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Применить Всего найдено 3960. Отображено 100.
10-06-2002 дата публикации

ПОТОЧНАЯ ЛИНИЯ ДЛЯ ПОЛУЧЕНИЯ ПЕНТАОКСИДА ВАНАДИЯ

Номер: RU0000023292U1

Поточная линия для получения пентаоксида ванадия, включающая последовательно установленные бак раствора щелочи, реактор для выщелачивания технического пентаоксида ванадия, нутч-фильтр для отделения нерастворимого остатка, реактор-кристаллизатор, фильтр-пресс и печь для разложения метаванадата аммония, отличающаяся тем, что дополнительно установлены реактор для выщелачивания нерастворимого остатка, снабженный баком-дозатором гипохлорита натрия и баком-нейтрализатором, снабженным баком-дозатором восстановителя, при этом реактор для выщелачивания нерастворимого остатка установлен между нутч-фильтром и реактором-кристаллизатором и соединен с баком раствора щелочи, а бак-нейтрализатор установлен на магистрали слива раствора из фильтр-пресса. (19) RU (11) 23 292 (13) U1 (51) МПК C01G 31/02 (2000.01) C22B 34/22 (2000.01) РОССИЙСКОЕ АГЕНТСТВО ПО ПАТЕНТАМ И ТОВАРНЫМ ЗНАКАМ (12) ОПИСАНИЕ ПОЛЕЗНОЙ МОДЕЛИ К СВИДЕТЕЛЬСТВУ (21), (22) Заявка: 2001130623/20 , 16.11.2001 (24) Дата начала отсчета срока действия патента: 16.11.2001 (46) Опубликовано: 10.06.2002 (73) Патентообладатель(и): ООО Научно-производственная экологическая фирма "ЭКО-технология" 2 3 2 9 2 (72) Автор(ы): Кудрявский Ю.П., Трапезников Ю.Ф., Глухих С.М., Казанцев В.П., Аликин В.И., Потеха С.И., Бездоля И.Н., Тарасенко В.В. R U Адрес для переписки: 618400, Пермская обл., г. Березники, ул. Деменева, 7, кв.3, Ю.П. Кудрявскому (71) Заявитель(и): ООО Научно-производственная экологическая фирма "ЭКО-технология" 2 3 2 9 2 R U (57) Формула полезной модели Поточная линия для получения пентаоксида ванадия, включающая последовательно установленные бак раствора щелочи, реактор для выщелачивания технического пентаоксида ванадия, нутч-фильтр для отделения нерастворимого остатка, реактор-кристаллизатор, фильтр-пресс и печь для разложения метаванадата аммония, отличающаяся тем, что дополнительно установлены реактор для выщелачивания нерастворимого остатка, снабженный баком-дозатором гипохлорита натрия и баком-нейтрализатором, ...

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10-10-2004 дата публикации

ПРОИЗВОДСТВЕННЫЙ УЧАСТОК ДЛЯ ПОЛУЧЕНИЯ ТОВАРНОГО ПЕНТАОКСИДА ВАНАДИЯ

Номер: RU0000041021U1

Производственный участок для получения товарного пентаоксида ванадия, включающий реактор для выщелачивания технологического пентаоксида ванадия, соединенный с баком для приготовления и подачи раствора щелочи, бак-дозатор для подачи в реактор раствора гипохлорида натрия, фильтр для отделения после выщелачивания нерастворимого остатка, бак-кристаллизатор метаванадата аммония, нижний слив которого направлен на фильтр, выход твердой фазы из которого имеет соединения с прокалочной печью, отличающийся тем, что дополнительно установлен бак-сборник маточного растворов и промвод метаванадата аммония, а после прокалочной печи абсорбер с ложным днищем и шаровой насадкой для очистки пылегазовой смеси, отходящей из прокалочной печи от соединений ванадия, абсорбер соединен через разбрызгивающие устройство с баком для приготовления и подачи раствора щелочи, сливной патрубок абсорбера через запорное устройство соединен с циркуляционным баком, нижний патрубок которого имеет соединения с разбрызгивающим устройством абсорбера и реактором для выщелачивания, бак-сборник маточных растворов и промвод соединен с реактором для обезвреживания стоков, один из верхних патрубков которого имеет соединение через дозатор с баком-сборником растворов, содержащих соли железа (II), а другой патрубок соединен с емкостью для щелочных реагентов, патрубок нижнего слива оксигидратной пульпы через запорную аппаратуру и транспортную магистраль соединен с дополнительно установленным фильтр-прессом для выделения из пульпы осадка оксигидратов металлов, корыто фильтра-пресса через шнековый питатель соединено со смесителем, в который направлены через дозирующие устройство и запорную аппаратуру, транспортную магистраль и трубопроводы из бункеров-дозаторов магнийсодержащий оксидные материалы, инертные наполнители, нерастворимый остаток и раствор, содержащего хлорид магния, смеситель имеет соединение с узлом формования, термообработки и отверждения композиционной смеси. РОССИЙСКАЯ ФЕДЕРАЦИЯ (19) RU (11) 41 021 (13) ...

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10-07-2008 дата публикации

АППАРАТУРНО-ТЕХНОЛОГИЧЕСКИЙ КОМПЛЕКС ДЛЯ ПОЛУЧЕНИЯ ПЕНТАОКСИДА ВАНАДИЯ

Номер: RU0000074636U1
Принадлежит: ООО "Энергострой"

Аппаратурно-технологический комплекс для получения пентаоксида ванадия, включающий реактор с мешалкой для щелочной обработки исходных ванадийсодержащих материалов, соединенный с баком для приготовления и подачи раствора гидроксида натрия, бак-кристаллизатор метаванадата аммония, фильтр - 1 для выделения осадка метаванадата аммония из суспензии и его промывки, прокалочную печь, бак-сборник маточных растворов и промвод метаванадата аммония, реактор для обезвреживания и нейтрализации ванадийсодержащих сточных вод, соединенный через дозатор с баком-сборником железо (II) - содержащих растворов и баком для приготовления и подачи раствора гидроксида натрия, реактор для обезвреживания и нейтрализации ванадийсодержащих сточных вод соединен с фильтром - 2, отличающийся тем, что реактор для щелочной обработки исходных ванадийсодержащих материалов имеет герметичное соединение с транспортируемой емкостью с окситрихлоридом ванадия, причем выход окситрихлорида ванадия из транспортируемой емкости через запорно-регулирующую арматуру направлен в распределительное устройство, расположенное в реакторе ниже уровня мешалки, бак-кристаллизатор имеет соединения с последовательно установленным баком-дозатором и расходно-накопительным баком для приготовления и подачи раствора хлорида аммония, на крышке бака-кристаллизатора имеется загрузочный люк, в который направлен выход из бункера-сборника хлорида натрия, после фильтра - 1 установлен бак-репульпатор метаванадата аммония, патрубок нижнего слива суспензии имеет соединение с фильтром - 1. РОССИЙСКАЯ ФЕДЕРАЦИЯ (19) RU (11) 74 636 (13) U1 (51) МПК C22B 34/22 (2006.01) C01G 31/02 (2006.01) ФЕДЕРАЛЬНАЯ СЛУЖБА ПО ИНТЕЛЛЕКТУАЛЬНОЙ СОБСТВЕННОСТИ, ПАТЕНТАМ И ТОВАРНЫМ ЗНАКАМ (12) ОПИСАНИЕ ПОЛЕЗНОЙ МОДЕЛИ К ПАТЕНТУ (21), (22) Заявка: 2008105007/22 , 11.02.2008 (24) Дата начала отсчета срока действия патента: 11.02.2008 (45) Опубликовано: 10.07.2008 (73) Патентообладатель(и): ООО "Энергострой" (RU) Ñòðàíèöà: 1 U 1 7 4 6 3 6 R U U 1 Формула полезной ...

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27-02-2009 дата публикации

ПРОМЫШЛЕННЫЙ УЧАСТОК ДЛЯ ПЕРЕРАБОТКИ НЕФТЕСОДЕРЖАЩИХ ОТХОДОВ

Номер: RU0000080838U1

Промышленный участок для переработки нефтесодержащих отходов, включающий приемные емкости, насосы, трубопроводы с запорно-регулирующей арматурой, промежуточные емкости с мешалками, соединенными с узлом для приготовления и дозировки химических реагентов для обработки нефтесодержащих отходов, выход из промежуточных емкостей направлен в трехфазную центрифугу, соединенную со сборниками нефтяной и водной фаз и контейнерами для сбора твердой фазы, выделенной из нефтесодержащих отходов, выход из которых соединен шнековым транспортером с питающим бункером, выход из которого направлен в камеру для термообработки, выполненной в виде наклонной вращающейся трубчатой печи, обогреваемой топочными газами и снабженной разгрузочным устройством, выход из которого направлен в сборники термообработанной твердой фазы, после которых установлена система брикетирования, отличающийся тем, что система брикетирования имеет соединения со шнековым смесителем, имеющим загрузочный люк для термообработанной твердой фазы, загрузочный люк, соединенный с бункером измельченного хлорида магния, вход в который направлен из узла дробления твердого хлорида магния, патрубок для подачи в смеситель магнезиального молока из обогреваемого реактора, снабженного перемешивающим устройством, конусом для загрузки магнийсодержащих оксидных материалов и патрубком для подвода в реактор воды, выход товарных продуктов из системы брикетирования оборудован разгрузочным устройством, направленным в расходно-накопительной емкостью. РОССИЙСКАЯ ФЕДЕРАЦИЯ (19) RU (11) (13) 80 838 U1 (51) МПК C01G 31/00 (2006.01) ФЕДЕРАЛЬНАЯ СЛУЖБА ПО ИНТЕЛЛЕКТУАЛЬНОЙ СОБСТВЕННОСТИ, ПАТЕНТАМ И ТОВАРНЫМ ЗНАКАМ (12) ОПИСАНИЕ ПОЛЕЗНОЙ МОДЕЛИ К ПАТЕНТУ (21), (22) Заявка: 2008146535/22, 25.11.2008 (24) Дата начала отсчета срока действия патента: 25.11.2008 (45) Опубликовано: 27.02.2009 (73) Патентообладатель(и): ООО Научно-производственная экологическая фирма "ЭКО-технология" (RU) U 1 8 0 8 3 8 R U Ñòðàíèöà: 1 ru CL U 1 Формула полезной модели ...

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10-03-2009 дата публикации

АППАРАТУРНО-ТЕХНОЛОГИЧЕСКАЯ СИСТЕМА ПРОИЗВОДСТВЕННОГО ОБОРУДОВАНИЯ ДЛЯ КОМПЛЕКСНОЙ ПЕРЕРАБОТКИ НЕФТЕСОДЕРЖАЩИХ ОТХОДОВ С ПОЛУЧЕНИЕМ ТОВАРНЫХ ПРОДУКТОВ

Номер: RU0000081185U1

Аппаратурно-технологическая система производственного оборудования для комплексной переработки нефтесодержащих отходов с получением товарных продуктов, включающая сборник исходных нефтесодержащих отходов, соединенный с обогреваемой емкостью, снабженной перемешивающим устройством, к которой подсоединен блок для приготовления и дозировки химических реагентов, высокоскоростную центрифугу, сборники очищенных от твердых частиц нефтяной и водной фаз, контейнеры для сбора осадка, устройство для термообработки осадка, сборник термообработанных осадков, склад готовой продукции, отличающаяся тем, что контейнеры для сбора осадка имеют соединения со смесителем, к которому подсоединен дозатор известняковой муки, получаемой на установке дробления и измельчения известнякового камня, в качестве устройства для термообработки осадка установлена вращающаяся трубчатая прокалочная печь, имеющая топку, соединенную со сборником нефтепродуктов, выделенных из исходных нефтесодержащих отходов, выход прокаленного материала из прокалочной печи через разгрузочный узел направлен в дробильно-размолочное отделение, имеющее фасовочную машину. РОССИЙСКАЯ ФЕДЕРАЦИЯ (19) RU (11) (13) 81 185 U1 (51) МПК C01G 31/00 (2006.01) ФЕДЕРАЛЬНАЯ СЛУЖБА ПО ИНТЕЛЛЕКТУАЛЬНОЙ СОБСТВЕННОСТИ, ПАТЕНТАМ И ТОВАРНЫМ ЗНАКАМ (12) ОПИСАНИЕ ПОЛЕЗНОЙ МОДЕЛИ К ПАТЕНТУ (21), (22) Заявка: 2008147318/22, 01.12.2008 (24) Дата начала отсчета срока действия патента: 01.12.2008 (45) Опубликовано: 10.03.2009 (73) Патентообладатель(и): ООО Научно-производственная экологическая фирма "ЭКО-технология" (RU) U 1 8 1 1 8 5 R U Ñòðàíèöà: 1 ru CL U 1 Формула полезной модели Аппаратурно-технологическая система производственного оборудования для комплексной переработки нефтесодержащих отходов с получением товарных продуктов, включающая сборник исходных нефтесодержащих отходов, соединенный с обогреваемой емкостью, снабженной перемешивающим устройством, к которой подсоединен блок для приготовления и дозировки химических реагентов, высокоскоростную ...

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10-06-2009 дата публикации

ПРОИЗВОДСТВЕННОЕ ОТДЕЛЕНИЕ ДЛЯ ПЕРЕРАБОТКИ ОКСИТРИХЛОРИДА ВАНАДИЯ С ПОЛУЧЕНИЕМ ПЕНТАОКСИДА ВАНАДИЯ

Номер: RU0000083497U1

Производственное отделение для переработки окситрихлорида ванадия с получением пентаоксида ванадия, включающее транспортируемую емкость с исходным окситрихлоридом ванадия, герметично соединенную через запорно-регулирующую арматуру с реактором, снабженным мешалкой и распределительным устройством для подачи окситрихлорида ванадия под слой раствора гидроксида натрия ниже уровня мешалки, реактор для разложения окситрихлорида ванадия соединен с последовательно установленным дозатором и баком для приготовления раствора гидроксида натрия, бак-кристаллизатор метаванадата аммония, снабженный мешалкой и оборудованный патрубком для подачи хлорида аммония, фильтр-1 для выделения из суспензии осадка метаванадата аммония и его промывки, бак-репульпатор метаванадата аммония, нижний слив из которого направлен на фильтр-1, после фильтра-1 для выделения из суспензии метаванадата аммония установлена прокалочная печь и бак-сборник маточных растворов и промвод метаванадата аммония, соединенный с реактором с мешалкой для обезвреживания ванадийсодержащих растворов и сточных вод, на крышке реактора имеются патрубки, один из которых подсоединен к дозатору и баку с раствором, содержащим хлорид железа (II), другой патрубок подсоединен к дозатору и баку для приготовления раствора гидроксида натрия, патрубок нижнего слива реактора имеет соединение через насос с фильтр-прессом 2 для выделения из пульпы осадка оксигидратов железа (II и III) с примесями соединений ванадия, отличающееся тем, что после реактора для разложения окситрихлорида ванадия установлен фильтр-пресс-3 для выделения из пульпы осадка оксигидрата титана, корыто фильтр-пресса-3 имеет разгрузочный люк, снабженный запорно-распределительным устройством, соединяющим фильтр-пресс-3 и бак-репульпатор осадка оксигидрата титана, имеющий подсоединения к фильтр-прессу-3 и дозатору раствора гидроксида натрия, выход очищенного от осадка растворов метаванадата натрия направлен в сборно-расходную емкость, соединенную с баком для кристаллизации ...

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10-06-2009 дата публикации

СИСТЕМА ТЕХНОЛОГИЧЕСКОГО ОБОРУДОВАНИЯ ДЛЯ ПЕРЕРАБОТКИ ОКСИТРИХЛОРИДА ВАНАДИЯ С ПОЛУЧЕНИЕМ ТОВАРНОГО ПЕНТАОКСИДА ВАНАДИЯ

Номер: RU0000083505U1

Система технологического оборудования для переработки окситрихлорида ванадия с получением пентаоксида ванадия, включающая реактор с мешалкой для щелочной обработки окситрихлорида ванадия, герметично соединенный с транспортируемой емкостью исходного технического окситрихлорида ванадия, последовательно соединенный с дозатором и баком для приготовления и подачи раствора гидроксида натрия, бак-кристаллизатор метаванадата аммония, соединенный с дозатором хлорида аммония и баком для приготовления раствора NHCl, фильтром-1 для выделения из суспензии осадка метаванадата аммония и его промывки, бак-репульпатор осадка метаванадата аммония, соединенный с фильтром-1, прокалочную печь, бак-сборник маточных растворов и промвод метаванадата аммония, реактор для обезвреживания от ванадия ванадийсодержащих сточных вод - маточных растворов и промвод метаванадата аммония, соединенный через дозатор с баком-сборником железо(II)-содержащих растворов, дозатором и баком для приготовления и подачи раствора гидроксида натрия, фильтр-2, для выделения из пульпы осадка оксигидратов железа (II и III) с примесями ванадия, отличающаяся тем, что патрубок нижнего слива реактора для щелочной обработки окситрихлорида ванадия направлен через насос и запорно-регулирующую арматуру на фильтр-3, корыто которого через разгрузочно-распределительное устройство соединено со сборником титанового кека-осадка оксигидрата титана, выход из которого направлен в обогреваемый бак с мешалкой для репульпации титанового кека, на крышке бака имеется патрубок для подсоединения к дозатору раствора гидроксида натрия, слив пульпы из бака через насос направлен на фильтр-3, выход очищенного от твердой фазы раствора метаванадата натрия из фильтра-3 направлен в сборно-усреднительную емкость, соединенную с реактором для щелочной обработки окситрихлорида ванадия, с баком-сборником маточных растворов и промвод метаванадата аммония, корыто фильтра-2 имеет соединения с загрузочным узлом, последовательно установленных сушильной камеры ...

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20-06-2009 дата публикации

ТЕХНОЛОГИЧЕСКИЙ ПЕРЕДЕЛ ДЛЯ ПОЛУЧЕНИЯ ПЕНТАОКСИДА ВАНАДИЯ

Номер: RU0000083774U1

Технологический передел для получения пентаоксида ванадия, включающий реактор с мешалкой для щелочной обработки окситрихлорида ванадия, герметично соединенный с транспортируемой емкостью исходного окситрихлорида ванадия и последовательно соединенный с дозатором и баком для приготовления и подачи раствора гидроксида натрия, бак-кристаллизатор метаванадата аммония соединен с дозатором хлорида аммония и баком для приготовления раствора хлорида аммония, фильтром-1 для выделения осадка метаванадата аммония из суспензии и его промывки, бак-репульпатор осадка метаванадата аммония, соединенный с фильтром-1, прокалочную печь, бак-сборник маточных растворов и промвод метаванадата аммония, реактор для обезвреживания от ванадия ванадийсодержащих сточных вод - маточных растворов и промвод метаванадата аммония, соединенный через дозатор с баком-сборником железо(II)-содержащих растворов, дозатором и баком для приготовления и подачи раствора гидроксида натрия, фильтр-2 для выделения из пульпы осадка оксигидратов железа (II и III) с примесями ванадия, отличающийся тем, что патрубок нижнего слива реактора для щелочной обработки окситрихлорида ванадия направлен через насос и запорно-регулирующую арматуру на фильтр-3, корыто которого через разгрузочно-распределительное устройство соединено со сборником титанового кека - осадка оксигидрата титана, выход из которого направлен в обогреваемый бак с мешалкой для репульпации титанового кека, на крышке бака имеется патрубок для подсоединения к дозатору раствора гидроксида натрия, слив пульпы из этого бака через насос направлен на фильтр-3, выход очищенного от твердой фазы раствора метаванадата натрия из фильтра-3 направлен в сборно-усреднительную емкость, соединенную с баком-кристаллизатором метаванадата аммония. РОССИЙСКАЯ ФЕДЕРАЦИЯ (19) RU (11) (13) 83 774 U1 (51) МПК C22B 34/22 (2006.01) C01G 31/02 (2006.01) ФЕДЕРАЛЬНАЯ СЛУЖБА ПО ИНТЕЛЛЕКТУАЛЬНОЙ СОБСТВЕННОСТИ, ПАТЕНТАМ И ТОВАРНЫМ ЗНАКАМ (12) ОПИСАНИЕ ПОЛЕЗНОЙ МОДЕЛИ К ПАТЕНТУ (21), (22) ...

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10-07-2009 дата публикации

ПОТОЧНАЯ ТЕХНОЛОГИЧЕСКАЯ ЛИНИЯ ДЛЯ ПЕРЕРАБОТКИ ОКСИТРИХЛОРИДА ВАНАДИЯ С ПОЛУЧЕНИЕМ ПЕНТАОКСИДА ВАНАДИЯ И УТИЛИЗАЦИЕЙ ОТХОДОВ ПРОИЗВОДСТВА

Номер: RU0000084383U1

Поточная технологическая линия для переработки окситрихлорида ванадия с получением пентаоксида ванадия и утилизацией отходов производства, включающая реактор для разложения окситрихлорида ванадия в щелочном растворе, соединенный через распределительное устройство с транспортируемой емкостью для окситрихлорида ванадия, бак с мешалкой для приготовления исходного раствора щелочи, сборно-расходную емкость раствора метаванадата щелочного металла, бак с мешалкой для приготовления исходного раствора хлорида аммония, линию раздачи дистиллированной воды, бак-кристаллизатор метаванадата аммония, фильтр - 1 для выделения из суспензии осадка метаванадата аммония, прокалочную печь, оборудованную затарочным узлом, баки-сборники ванадийсодержащих маточных растворов и промвод, установку для извлечения из маточных растворов и промвод соединений ванадия, в состав которой входит баковое оборудование, реакторы, дозатор химических реагентов, фильтры, трубопроводы, сушильная камера и/или прокалочная печь, насосы, запорно-регулирующая арматура, сборная емкость для очищенных от соединений ванадия хлоридных растворов, отличающаяся тем, что реактор для разложения окситрихлорида ванадия имеет соединение с баком для приготовления и подачи солевого раствора гидроксида калия, соединенного с фильтр-прессом - 2 и баком с исходным раствором гидроксида калия, бак-кристаллизатор метаванадата аммония соединен с сборно-расходным баком фильтратов - растворов метаванадата калия после выделения осадка оксигидрата титана и с баком для приготовления и подачи смешанного раствора хлоридов аммония и калия, патрубок нижнего слива пульпы из реактора для разложения технического окситрихлорида ванадия в солевом растворе гидроксида калия соединен с входным патрубком фильтр-пресса - 2, выход из которого твердой фазы - осадка оксигидрата титана через корыто фильтр-пресса - 2 направлен в бак-репульпатор оксигидрата титана, соединенный с баком для приготовления и подачи раствора гидроксида калия, выход твердой фазы из ...

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03-05-2012 дата публикации

Mixed valency metal sulfide sorbents for heavy metals

Номер: US20120103912A1
Принадлежит: JOHNSON MATTHEY PLC

A sorbent, suitable for removing heavy metals, including mercury, from fluids containing hydrogen and/or carbon monoxide at temperatures up to 550° C., in the form of a shaped unit comprising one or more mixed-valency metal sulphides of vanadium, chromium, manganese, iron, cobalt or nickel.

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28-06-2012 дата публикации

Positive electrode active material for secondary battery and magnesium secondary battery using the same

Номер: US20120164537A1
Принадлежит: HITACHI LTD

In a positive electrode active material for a magnesium secondary battery and a magnesium secondary battery using it, there is contained a powder particle containing a crystal phase having a structure formed with aggregation of a plurality of crystallites, and amorphous phases formed between the crystallites themselves; the amorphous phases contain at least one kind of a metal oxide selected from a vanadium oxide, an iron oxide, a manganese oxide, a nickel oxide and a cobalt oxide; and the crystal phase and the amorphous phases use the positive electrode active material enabling to store and release magnesium ions.

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01-11-2012 дата публикации

Synthesis of Nanoparticles by Means of Ionic Liquids

Номер: US20120275991A1

A method for producing nanoscale particles by means of ionic liquids produces highly crystalline particles. The ionic liquids can be easily regenerated.

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27-12-2012 дата публикации

Nanostructures, their use and process for their production

Номер: US20120329686A1
Принадлежит: Yeda Research and Development Co Ltd

A lubricating and shock absorbing materials are described, which are based on nanoparticles having the formula A 1-x -B x -chalcogenide. Processes for their manufacture are also described.

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17-01-2013 дата публикации

Positive electrode active material

Номер: US20130015410A1
Принадлежит: Hitachi Chemical Co Ltd, HITACHI LTD

A lithium ion secondary battery has a high cycle retention rate, and has its battery capacity increased. A positive electrode active material is used which includes a crystal phase having a structure formed by collecting a plurality of crystallites 101 , and powder particles containing amorphous phases 103 a and 103 b formed between the crystallites 101 . The amorphous phases 103 a and 103 b contain one or more kinds of metal oxides selected from the group consisting of vanadium oxide, iron oxide, manganese oxide, nickel oxide and cobalt oxide. The crystal phase and the amorphous phase 103 a and 103 b are capable of intercalation and deintercalation of lithium ions.

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11-04-2013 дата публикации

CHIRAL NEMATIC NANOCRYSTALLINE METAL OXIDES

Номер: US20130089492A1
Принадлежит:

A mesoporous metal oxide materials with a chiral organization; and a method for producing it, in the method a polymerizable metal oxide precursor is condensed inside the pores of chiral nematic mesoporous silica by the so-called “hard templating” method. As a specific example, mesoporous titanium dioxide is formed inside of a chiral nematic silica film templated by nanocrystalline cellulose (NCC). After removing the silica template such as by dissolving the silica in concentrated aqueous base, the resulting product is a mesoporous titania with a high surface area. These mesoporous metal oxide materials with high surface area and chiral nematic structures that lead to photonic properties may be useful for photonic applications as well as enantioselective catalysis, photocatalysis, photovoltaics, UV filters, batteries, and sensors. 1. A mesoporous metal oxide having chirality and crystallinity.2. The mesoporous metal oxide of claim 1 , wherein said oxide is titanium oxide.3. The mesoporous metal oxide of claim 2 , wherein said titanium oxide is anatase titanium oxide.4. The mesoporous metal oxide of claim 1 , wherein said chirality is in a length scale ranging from nanometers to centimetres.5. The mesoporous metal oxide of claim 2 , wherein said chirality is in a length scale ranging from nanometers to centimetres.6. A process for producing a mesoporous metal oxide having chirality claim 2 , comprising: introducing a metal oxide precursor into a mesoporous silica template defining chirality claim 2 , converting said precursor to metal oxide claim 2 , and removing said silica template.7. A process according to claim 6 , wherein said precursor is a precursor of a metal oxide selected from the group consisting of titanium oxide claim 6 , tin dioxide claim 6 , iron oxide claim 6 , tantalum oxide and vanadium oxide.8. A process according to claim 6 , wherein said precursor is a precursor of titanium oxide.9. A process according to claim 6 , wherein said precursor is a ...

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25-04-2013 дата публикации

Doped Nanoparticles and Methods of Making and Using Same

Номер: US20130101848A1

Doped nanoparticles, methods of making such nanoparticles, and uses of such nanoparticles. The nanoparticles exhibit a metal-insulator phase transition at a temperature of −200° C. to 350° C. The nanoparticles have a broad range of sizes and various morphologies. The nanoparticles can be used in coatings and in device structures.

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25-04-2013 дата публикации

METHOD OF MANUFACTURING METAL OXIDE FILM, METAL OXIDE FILM, ELEMENT USING THE METAL OXIDE FILM, SUBSTRATE WITH METAL OXIDE FILM, AND DEVICE USING THE SUBSTRATE WITH METAL OXIDE FILM

Номер: US20130101867A1
Принадлежит: SUMITOMO METAL MINING CO., LTD.

Provided is a method of manufacturing a metal oxide film to be formed through the following processes: a coating process of forming a coating film on a substrate by using a coating liquid for forming metal oxide film containing any of various organometallic compounds; a drying process of making the coating film into a dried coating film; and a heating process of forming an inorganic film from the dried coating film under an oxygen-containing atmosphere having a dew-point temperature equal to or lower than −10° C. 1. A method of manufacturing a metal oxide film to be formed through the following processes: a coating process of coating a substrate with a coating liquid for forming metal oxide film containing an organometallic compound as a main component to form a coating film; a drying process of drying the coating film to form a dried coating film; and a heating process of mineralizing the dried coating film to form an inorganic film having an inorganic component , which is a metal oxide , as a main component , whereinthe heating process is a process of performing a heating treatment to elevate a temperature of the dried coating film, which has the organometallic compound as a main component and has been formed in the drying process, up to a temperature or higher at which at least mineralization of the organometallic compound components occurs, under an oxygen-containing atmosphere having a dew-point temperature equal to or lower than −10° C., and then removing an organic component contained in the dried coating film by thermal decomposition, burning, or thermal decomposition and burning, thereby forming a metal oxide fine-particle layer densely packed with metal oxide fine particles having a metal oxide as a main component, andthe organometallic compound is formed of any one or more types of an organic aluminum compound, an organic silicon compound, an organic scandium compound, an organic titanium compound, an organic vanadium compound, an organic chromium ...

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20-06-2013 дата публикации

H4v3o8, a new vanadium(iv) oxide electroactive material for aqueous and non aqueous batteries

Номер: US20130157138A1
Принадлежит: BELENOS CLEAN POWER HOLDING AG

A new electroactive material of formula H 4 V 3 O 8 obtainable from H 2 V 3 O 8 is described as well as a method for its production, an electroactive cathode coating material comprising this electroactive material, a method for its production and cathodes as well as aqueous and non aqueous, rechargeable and non rechargeable batteries comprising such cathodes.

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29-08-2013 дата публикации

Re-Dispersible Metal Oxide Nanoparticles and Method of Making Same

Номер: US20130220178A1
Принадлежит: Justus Liebig Universitaet Giessen

The current invention relates to a method of making metal oxide nanoparticles comprising the reaction of—at least one metal oxide precursor (P) containing at least one metal (M) with—at least one monofunctional alcohol (A) wherein the hydroxy group is bound to a secondary, tertiary or alpha-unsaturated carbon atom—in the presence of at least one aliphatic compound (F) according to the formula Y 1 —R 1 —X—R 2 —Y 2 , wherein—R 1 and R 2 each are the same or different and independently selected from aliphatic groups with from 1 to 20 carbon atoms, —Y 1 and Y 2 each are the same or different and independently selected from OH, NH 2 and SH, and —X is selected from the group consisting of chemical bond, —O—, —S—, —NR 3 —, and CR 4 R 5 , wherein R 3 , R 4 and R 5 each are the same or different and represent a hydrogen atom or an aliphatic group with from 1 to 20 carbon atoms which optionally carries functional groups selected from OH, NH 2 and SH. This invention also relates to metal oxide nanoparticles, to a method of making dispersions of said nanoparticles and to dispersions containing them.

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06-03-2014 дата публикации

SOLUTION-PROCESSED TRANSITION METAL OXIDES

Номер: US20140061550A1
Принадлежит:

Embodiments may pertain to methods for preparing a transition metal oxide. 1. A method comprising:combining a peroxide with a solution of an alcohol-based solvent and a transition metal; and2. The method of claim 1 , wherein said peroxide comprises hydrogen peroxide.3. The method of claim 1 , wherein said alcohol-based solvent is ethanol.4. The method of claim 1 , wherein said solution comprises:an amount of said alcohol-based solvent to affect a rate of reaction of said transition metal with said peroxide in combination.5. The method of claim 1 , wherein said transition metal comprises one of the group consisting essentially of vanadium claim 1 , molybdenum claim 1 , tungsten.6. The method of claim 1 , further comprising:drying said solution of said peroxide and said transition metal to form an at least partially dried transition metal oxide.7. The method of claim 6 , further comprising:combining at least one water-free solvent with said at least partially dried transition metal oxide.8. The method of claim 6 , the said drying comprises:creating said at least partially dried transition metal oxide in a vacuum environment.9. The method of claim 6 , further comprising:dispersing said at least partially dried transition metal oxide into a water-free solvent.10. The method of claim 9 , further comprising:forming a transition metal oxide film.11. The method of claim 10 , said forming comprises:spin-coating said dispersed solution onto a substrate to form said transition metal oxide film.12. The method of claim 11 , further comprising:forming an organic device that includes said transition metal oxide film.13. The method of claim 12 , wherein said organic device comprises at least one of an organic light emitting diode claim 12 , an organic solar cell claim 12 , or an organic photodetector.14. The method of claim 10 , wherein said forming comprisesannealing said transition metal oxide film at a temperature approximately between approximately 60.0° C. and approximately ...

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20-03-2014 дата публикации

VANADIUM OXIDE PURIFICATION PROCESS

Номер: US20140079609A1
Автор: Drozd Michael Adam
Принадлежит:

Process for purifying vanadium oxide that includes cationic exchange resin and solvent extraction. 1. A process for purifying vanadium oxide , comprising:(a) loading vanadium oxide on a cationic exchange resin by contacting a first vanadium oxide-containing aqueous solution with the resin to provide a cationic exchange resin loaded with vanadium oxide;(b) stripping vanadium oxide from the cationic resin loaded with vanadium oxide by contacting the cationic exchange resin loaded with vanadium oxide with acid to regenerate the resin and to provide a second vanadium oxide-containing aqueous solution, wherein the concentration of vanadium oxide in the second solution relative to other cationic metals is greater than in the first solution;(c) extracting the second vanadium oxide-containing aqueous solution with an organic solvent comprising a chelating agent to provide an aqueous solution and an organic solvent containing vanadium oxide;(d) separating the organic solvent containing vanadium oxide from the aqueous solution; and(e) releasing vanadium oxide from the organic solvent by contacting the organic solvent containing vanadium oxide with an aqueous solution to provide a third vanadium oxide-containing aqueous solution, wherein the concentration of vanadium oxide in the third solution relative to other cationic metals is greater than in the second solution.2. The process of further comprising:(f) extracting the third vanadium oxide-containing aqueous solution with an organic solvent comprising a chelating agent to provide an aqueous solution and an organic solvent containing vanadium oxide;(g) separating the organic solvent containing vanadium oxide from the aqueous solution; and(h) releasing vanadium oxide from the organic solvent by contacting the organic solvent containing vanadium oxide with an aqueous solution to provide a fourth vanadium oxide-containing aqueous solution, wherein the concentration of vanadium oxide in the fourth solution relative to other ...

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04-01-2018 дата публикации

System and Method for Purifying Vanadium Pentoxide

Номер: US20180002190A1
Принадлежит:

The present invention provides a system and method for purifying vanadium pentoxide. Industrial grade vanadium pentoxide is converted to vanadium oxytrichloride by low temperature fluidizing chlorination, wherein chlorinating gas is preheated via heat exchange between fluidizing gas and chlorination flue gas, and an appropriate amount of air is added to enable a part of carbon powder to combust so as to achieve a balanced heat supply during the chlorination, thereby increasing the efficiency of chlorination and ensuring good selectivity in low temperature chlorination. The vanadium oxytrichloride is purified by rectification, and then subjected to plasma oxidation, thereby obtaining a high-purity vanadium pentoxide product and chlorine gas. The chlorine gas is returned for low temperature chlorination. The system and method have advantages of favorable adaptability to raw material, no discharge of contaminated wastewater, low energy consumption and chlorine consumption in production, stable product quality, etc. 1. A system for purifying vanadium pentoxide , comprising a feeding device , a low temperature chlorination fluidized bed , a rectification and purification device , a plasma oxidation device , a tail gas washing absorber , an induced draft fan and a chimney;wherein the feeding device comprises an industrial grade vanadium pentoxide hopper, an industrial grade vanadium pentoxide screw feeder, a carbon powder hopper and a carbon powder screw feeder;the low temperature chlorination fluidized bed comprises a chlorination bed feeder, a chlorination fluidized bed body, a chlorination bed cyclone separator, a flue gas heat exchanger, a flue gas condenser, a chlorination bed acid-seal tank and a chlorination bed spiral slag-discharging device;the rectification and purification device comprises a distilling still, a rectifying column, a distillate condenser, a reflux liquid collecting tank, a silicon-containing vanadium oxytrichloride storage tank, a rectification ...

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07-01-2016 дата публикации

METHOD OF PREPARING A VANADIUM OXIDE COMPOUND AND USE THEREOF IN ELECTROCHEMICAL CELLS

Номер: US20160006028A1
Принадлежит:

Electrochemical cell comprising an anode and a cathode is provided. The anode and the cathode independently comprises or consists essentially of a vanadium oxide compound having general formula MVO, wherein M is selected from the group consisting of ammonium, alkali-metal, and alkaline-earth metal; and n is 1 or 2. Method of preparing a vanadium oxide compound having general formula MVOis also provided. 1. An electrochemical cell comprising an anode and a cathode , wherein the anode and the cathode independently comprises a vanadium oxide compound of general formula (I){'br': None, 'sub': n', '6', '16, 'MVO\u2003\u2003(I),'}wherein M is selected from the group consisting of ammonium, alkali-metal, and alkaline-earth metal; and n is 1 or 2.2. The electrochemical cell according to claim 1 , wherein M is selected from the group consisting of ammonium claim 1 , sodium claim 1 , potassium claim 1 , lithium claim 1 , calcium and magnesium.34.-. (canceled)5. The electrochemical cell according to claim 1 , wherein the vanadium oxide compound is a nanostructured vanadium oxide compound comprising nanobelts claim 1 , nanorods claim 1 , microrods claim 1 , nanofibers claim 1 , or combinations thereof.6. The electrochemical cell according to claim 5 , wherein the nanobelts have an average diameter in the range of about 50 nm to about 100 nm.7. The electrochemical cell according to claim 5 , wherein the nanorods have an average length in the range of about 1 μm to about 10 μm.8. The electrochemical cell according to claim 1 , wherein the anode and the cathode independently further comprise a binder.9. (canceled)10. The electrochemical cell according to claim 1 , wherein the anode and the cathode independently further comprise an electrically conductive agent.1112.-. (canceled)13. The electrochemical cell according to claim 10 , wherein the weight ratio of vanadium oxide compound:binder:electrically conductive agent is about 75:15:10.14. The electrochemical cell according to ...

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04-01-2018 дата публикации

A METAL OXIDE NANOSTRUCTURED MATERIAL AND AN ELECTROCHEMICAL CELL COMPRISING THE SAME

Номер: US20180005771A1
Автор: LEE Pooi See, WANG Xu
Принадлежит:

A method for preparing a niobium, titanium or vanadium metal oxide nanostructured material is provided. The method comprises providing an aqueous reagent comprising (i) a soluble metal oxalate, and/or (ii) oxalic acid and a metal oxide precursor, adding a buffering agent to the aqueous reagent to form a mixture, and heating the mixture under hydrothermal conditions to obtain the metal oxide nanostructured material. The metal oxide nanostructured material may also be doped with a dopant metal such as titanium to enhance capacity and cycling stability. An electrode comprising the metal oxide nanostructured material, and an electrochemical cell containing the electrode are also provided. 1. A method for preparing a metal oxide nanostructured material , the method comprisinga) providing an aqueous reagent comprising (i) a soluble metal oxalate, and/or (ii) oxalic acid and a metal oxide precursor,b) adding a buffering agent to the aqueous reagent to form a mixture, andc) heating the mixture under hydrothermal conditions to obtain the metal oxide nanostructured material.2. The method according to claim 1 , wherein the metal oxide nanostructured material comprises an orthorhombic crystal structure.3. The method according to claim 1 , wherein metal of the metal oxide nanostructured material is selected from the group consisting of niobium claim 1 , titanium claim 1 , vanadium claim 1 , combinations thereof claim 1 , and alloys thereof.4. (canceled)5. The method according to claim 1 , wherein the soluble metal oxalate is selected from the group consisting of niobium (V) oxalate claim 1 , titanium oxalate claim 1 , vanadium oxalate claim 1 , ammonium niobium (V) oxalate claim 1 , ammonium titanium oxalate claim 1 , ammonium vanadium oxalate claim 1 , potassium titanium oxide oxalate claim 1 , and mixtures thereof.6. The method according to claim 1 , wherein the metal oxide precursor is selected from the group consisting of metal halides claim 1 , metal sulfates claim 1 , ...

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04-01-2018 дата публикации

Ceramic material, method for producing the ceramic material, and electroceramic component comprising the ceramic material

Номер: US20180006210A1
Принадлежит: EPCOS AG

The invention relates to a ceramic material, comprising lead zirconate titanate, which additionally contains K and optionally Cu. The ceramic material can be used in an electroceramic component, for example a piezoelectric actuator. The invention also relates to methods for producing the ceramic material and the electronic component.

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11-01-2018 дата публикации

SYSTEM AND METHOD FOR PURIFYING AND PREPARING HIGH-PURITY VANADIUM PENTOXIDE POWDER

Номер: US20180009673A1
Принадлежит:

The present invention provides a system and method for purifying and preparing vanadium pentoxide powder. Industrial grade vanadium pentoxide is converted to vanadium oxytrichloride by low temperature fluidizing chlorination, wherein chlorinating gas is preheated via heat exchange between fluidizing gas and chlorination flue gas, and an appropriate amount of air is added to enable a part of carbon powder to combust so as to achieve a balanced heat supply during the chlorination, thereby increasing the efficiency of chlorination and ensuring good selectivity in low temperature chlorination. The vanadium oxytrichloride is purified by rectification, and then subjected to fluidized gas phase ammonification, thereby obtaining ammonium metavanadate, and further obtaining a high-purity vanadium pentoxide powder product through fluidized calcination. The system and method have advantages of favorable adaptability to a raw material, no discharge of contaminated wastewater, low energy consumption and chlorine consumption in production, stable product quality and so on. 1. A system for purifying and preparing high-purity vanadium pentoxide powder , comprising a feeding device , a low temperature chlorination fluidized bed , a rectification and purification device , a gas phase ammonification fluidized bed , an ammonium metavanadate feeding device , a calcination fluidized bed , a tail gas washing absorber , an induced draft fan and a chimney;wherein the feeding device comprises an industrial grade vanadium pentoxide hopper, an industrial grade vanadium pentoxide screw feeder, a carbon powder hopper and a carbon powder screw feeder;the low temperature chlorination fluidized bed comprises a chlorination bed feeder, a chlorination fluidized bed body, a chlorination bed cyclone separator, a flue gas heat exchanger, a flue gas condenser, a chlorination bed acid-seal tank and a chlorination bed spiral slag-discharging device;the rectification and purification device comprises a ...

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11-01-2018 дата публикации

SYSTEM AND METHOD FOR PRODUCING HIGH-PURITY VANADIUM TETRAOXIDE POWDER

Номер: US20180009674A1
Принадлежит:

The present invention provides a system and method for producing high-purity vanadium tetraoxide powder. Industrial grade vanadium pentoxide is converted to vanadium oxytrichloride by low temperature fluidizing chlorination, wherein chlorinating gas is preheated via heat exchange between fluidizing gas and chlorination flue gas, and an appropriate amount of air is added to enable a part of carbon powder to combust so as to achieve a balanced heat supply during the chlorination, thereby increasing the efficiency of chlorination and ensuring good selectivity in low temperature chlorination. The vanadium oxytrichloride is purified by rectification, and then subjected to fluidized gas phase hydrolyzation, thereby producing a high-purity vanadium pentoxide product and a by-product solution of hydrochloric acid, and further obtaining a high-purity vanadium tetraoxide powder product through fluidized hydrogen reduction. The system and method have advantages of favorable adaptability to raw material, no discharge of contaminated wastewater, low energy consumption, etc. 1. A system for producing high-purity vanadium tetraoxide powder ,comprising a feeding device, a low temperature chlorination fluidized bed, a rectification and purification device, a gas phase hydrolyzation fluidized bed, a high-purity vanadium pentoxide feeding device, a reduction fluidized bed, a tail gas washing absorber, an induced draft fan and a chimney;wherein the feeding device comprises an industrial grade vanadium pentoxide hopper, an industrial grade vanadium pentoxide screw feeder, a carbon powder hopper and a carbon powder screw feeder;the low temperature chlorination fluidized bed comprises a chlorination bed feeder, a chlorination fluidized bed body, a chlorination bed cyclone separator, a flue gas heat exchanger, a flue gas condenser, a chlorination bed acid-seal tank and a chlorination bed spiral slag-discharging device;the rectification and purification device comprises a distilling still, ...

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11-01-2018 дата публикации

System and Method for Producing High-Purity Vanadium Pentoxide Powder

Номер: US20180009675A1
Принадлежит:

The present invention provides a system and method for producing high-purity vanadium pentoxide powder. Industrial grade vanadium pentoxide is converted to vanadium oxytrichloride by low temperature fluidizing chlorination, wherein chlorinating gas is preheated via heat exchange between fluidizing gas and chlorination flue gas, and an appropriate amount of air is added to enable a part of carbon powder to combust so as to achieve a balanced heat supply during the chlorination, thereby increasing the efficiency of chlorination and ensuring good selectivity in low temperature chlorination. The vanadium oxytrichloride is purified by rectification, and then subjected to fluidized gas phase hydrolyzation and fluidized calcination, thereby producing a high-purity vanadium pentoxide product and a by-product of hydrochloric acid solution. The system and method have advantages of favorable adaptability to raw material, no discharge of contaminated wastewater, low energy consumption in production, low operation cost, stable product quality, etc. 1. A system for producing high-purity vanadium pentoxide powder , comprising a feeding device , a low temperature chlorination fluidized bed , a rectification and purification device , a gas phase hydrolyzation fluidized bed , a calcination fluidized bed , a tail gas washing absorber , an induced draft fan and a chimney;wherein the feeding device comprises an industrial grade vanadium pentoxide hopper, an industrial grade vanadium pentoxide screw feeder, a carbon powder hopper and a carbon powder screw feeder;the low temperature chlorination fluidized bed comprises a chlorination bed feeder, a chlorination fluidized bed body, a chlorination bed cyclone separator, a flue gas heat exchanger, a flue gas condenser, a chlorination bed acid-seal tank and a chlorination bed spiral slag-discharging device;the rectification and purification device comprises a distilling still, a rectifying column, a distillate condenser, a reflux liquid ...

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14-01-2021 дата публикации

ENAMEL COMPOSITION, METHOD FOR PREPARING ENAMEL COMPOSITION, AND COOKING APPLIANCE

Номер: US20210009814A1
Принадлежит:

A cooking appliance includes a chamber surface that defines a cavity including a cooking chamber, a door that is configured to open and close the cavity and has a door surface configured to face the cavity, a heat source configured to supply heat to the cavity, and a coating layer disposed on the chamber surface or the door surface. The coating layer includes an enamel composition of materials including 30 to 45 wt % of phosphorus pentoxide (PO), 5 to 20 wt % of silicon dioxide (SiO), 15 to 30 wt % of aluminum oxide (AlO), 10 to 20 wt % of zirconium dioxide (ZrO), 5 to 20 wt % of at least one of lithium oxide (LiO), sodium oxide (NO), or potassium oxide (KO), 5 to 15 wt % of boron trioxide (BO), and10 to 25 wt % of vanadium pentoxide (VO). 1. A cooking appliance , comprising:a chamber surface that defines a cavity including a cooking chamber;a door configured to open and close the cavity, the door having a door surface configured to face the cavity;a heat source configured to supply heat to the cavity; anda coating layer disposed on the chamber surface or the door surface, the coating layer comprising an enamel composition of materials, [{'sub': 2', '5, '30 to 45 wt % of phosphorus pentoxide (PO),'}, {'sub': '2', '5 to 20 wt % of silicon dioxide (SiO),'}, {'sub': 2', '3, '15 to 30 wt % of aluminum oxide (AlO),'}, {'sub': '2', '10 to 20 wt % of zirconium dioxide (ZrO),'}, {'sub': 2', '2', '2, '5 to 20 wt % of at least one of lithium oxide (LiO), sodium oxide (NaO), or potassium oxide (KO),'}, {'sub': 2', '3, '5 to 15 wt % of boron trioxide (BO), and'}, {'sub': 2', '5, '10 to 25 wt % of vanadium pentoxide (VO).'}], 'wherein the enamel composition comprises2. The cooking appliance of claim 1 , wherein the enamel composition further comprises:{'sub': '2', '5 or less wt % of titanium dioxide (TiO); and'}10 or less wt % of at least one of stannous oxide (SnO) or zinc oxide (ZnO).3. The cooking appliance of claim 1 , further comprising a metal plate that defines the ...

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11-01-2018 дата публикации

SECONDARY BATTERY AND METHOD OF MANUFACTURING THE SAME, BATTERY PACK, ELECTRIC VEHICLE, ELECTRIC POWER STORAGE SYSTEM, ELECTRIC POWER TOOL, AND ELECTRONIC APPARATUS

Номер: US20180013143A1
Принадлежит:

There is provided a secondary battery including a cathode, an anode including an anode active material layer and a coating film, and an electrolytic solution. The anode active material layer includes a titanium-containing compound, and a surface of the anode active material layer is coated with the coating film. The electrolytic solution includes one or more of unsaturated cyclic carbonate esters. Porosity of a portion of the anode active material layer measured with use of a mercury intrusion technique is within a range from 30% to 50% both inclusive. The portion of the anode active material layer is cut together with a portion of the coating film from a surface of the coating film to a depth of 10 μm. 2. The secondary battery according to claim 1 , wherein a peak is detected by analysis of the coating film with use of Fourier transform infrared spectroscopy in each of a wave number range smaller than 1000 cm claim 1 , and a wave number range larger than 2000 cm claim 1 , and a peak is not detected in a wave number range from 1000 cm to 2000 cmboth inclusive.3. The secondary battery according to claim 1 , wherein the titanium-containing compound includes one or more of a titanium oxide represented by the following formula (1) and respective lithium-titanium composite oxides represented by the following formulas (2) to (4) claim 1 ,{'br': None, 'sub': 'w', 'TiO\u2003\u2003(1)'} {'br': None, 'sub': x', '(1−3x)/2', '(3+x)/2', '4, 'Li[LiM1Ti]O\u2003\u2003(2)'}, 'where w satisfies 1.85≦w2.15.'} {'br': None, 'sub': y', '1-3y', '1+23', '4, 'Li[LiM2Ti] O(3)'}, 'where M1 is one or more of magnesium (Mg), calcium (Ca), copper (Cu), zinc (Zn), and strontium (Sr), and “x” satisfies 0≦x≦1/3,'} {'br': None, 'sub': 1/3', 'z', '(5/3)-z', '4, 'Li[LiM3Ti]O\u2003\u2003(4)'}, 'where M2 is one or more of aluminum (Al), scandium (Sc), chromium (Cr), manganese (Mn), iron (Fe), germanium (Ga), and yttrium (Y), and “y” satisfies 0≦y≦1/3, and'}where M3 is one or more of vanadium (V), ...

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18-01-2018 дата публикации

Polymer-Metal Compound Composite Ink, and Preparation Method and Application Thereof

Номер: US20180016456A1
Принадлежит:

The present invention discloses a polymer-metal compound composite ink, a preparation method and application thereof. The composite ink comprises: at least one polymer; at least one metal compound material, the metal compound material being selected from polyoxometalate compounds and nanocrystalline metal oxides; at least one solvent which is used for forming a disperse system in the form of a uniform fluid together with the remaining components in the composite ink. The present invention also discloses a method for preparing the composite ink. The composite ink of the present invention is easily available in raw material, easy to prepare and low in cost, and can be manufactured into a composite thin film by spin-coating, printing or in other ways. The composite thin film, as an electrode modification layer, can be applied to photoelectric devices such as solar cells or light-emitting diodes, so as to improve the contact performance between an electrode and an organic active layer and thus enhance the performance and yield of photoelectric devices. 1. A polymer-metal compound composite ink , comprising:at least one polymer;at least one metal compound material, the metal compound material being selected from polyoxometalate compounds and nanocrystalline metal oxides; andat least one solvent which is used for forming a disperse system in the form of a uniform fluid together with the remaining components in the composite ink.2. The polymer-metal compound composite ink according to claim 1 , characterized in that the polyoxometalate compound is at least selected from polyoxometalate compounds comprising any one of or a combination of more than two of molybdenum claim 1 , tungsten and vanadium.3. The polymer-metal compound composite ink according to claim 2 , characterized in that the polyoxometalate compound further contains any one of or a combination of more than two of phosphorus claim 2 , silicon claim 2 , germanium and arsenicum.4. The polymer-metal compound ...

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21-01-2021 дата публикации

PROCESS FOR OBTAINING VANADIUM OXIDE FROM A GASIFIER SLAG FIELD

Номер: US20210017038A1
Принадлежит: RELIANCE INDUSTRIES LIMITED

A process for obtaining vanadium component in the form of vanadium oxide from gasifier slag is disclosed. The process comprises pulverizing the slag to obtain pulverized slag, which is blended with water and an alkali salt to obtain a slurry. The slurry is dried and then roasted in the presence of air to obtain a roasted slag. The roasted slag is leached to obtain a first filtrate comprising the vanadium component. The first filtrate is reacted with a magnesium salt to remove a silica component in the form of a precipitate. The silica free second filtrate is reacted with an ammonium salt to obtain ammonium metavanadate, which is further calcined to obtain the significant amount of vanadium pentoxide (VO). 1. A process for obtaining vanadium oxide from gasifier slag having vanadium component;the process comprising the following steps:a) pulverizing the gasifier slag to a particle size less than 100 μm to obtain a pulverized slag;b) blending the pulverized slag with water and at least one alkali salt to obtain a slurry;c) drying the slurry to remove water therefrom;d) roasting the dried slurry in the presence of air and at a temperature in the range of 750° C. to 1000° C. to obtain a roasted slag;e) leaching the roasted slag with water to obtain a first filtrate comprising the vanadium component;f) separating a silica component from the first filtrate to obtain a second filtrate;g) reacting the second filtrate with an ammonium salt to obtain ammonium metavanadate in the form of a precipitate; andh) separating the precipitate and calcining at a temperature in the range of 400 to 600° C. to obtain vanadium oxide having purity greater than 95%.2. The process as claimed in claim 1 , wherein in the step (b) the alkali salt is at least one selected from the group consisting of sodium carbonate (NaCO) and sodium sulphate (NaSO) and the amount of the alkali salt is in the range of 20 wt % to 50 wt % of the total slag.3. The process as claimed in claim 1 , wherein in the step ...

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21-01-2021 дата публикации

CARBON NANOFIBER ADHESIVE FILM

Номер: US20210017674A1
Принадлежит: Lintec Of America, Inc.

A filtered nanofiber film can be used as an intervening layer between the nanofiber structure (e.g., a drawn nanofiber sheet and/or a nanofiber forest) and a final substrate. Filtered nanofiber films can adhere to other types of nanofiber structures (e.g., drawn nanofiber sheets and/or nanofiber forests) and also exhibit adhesion to non-nanofiber surfaces. Thus, when used as an intervening layer between another type of nanofiber structure and a final substrate, a filtered film can increase adhesion therebetween. Filtered nanofiber films can also be used as a releasable protective film to prevent contamination of a confronting major surface of the nanofiber structure. 1. A method comprising:providing a nanofiber structure having an exposed major surface, the nanofiber structure comprising an array of aligned nanofibers;providing a filtered nanofiber film having a first major surface and a second major surface;placing the first major surface of the filtered nanofiber film in contact with the exposed major surface of the nanofiber structure;placing the second major surface of the filtered nanofiber film in contact with a final substrate; andresponsive to placing the second major surface of the filtered nanofiber film in contact with the final substrate, adhering the nanofiber structure to the final substrate via the filtered nanofiber film.2. The method of claim 1 , wherein the array of aligned nanofibers comprises a nanofiber forest or a drawn nanofiber sheet.3. The method of claim 2 , further comprising densifying the drawn nanofiber sheet by exposing the drawn nanofiber sheet to a solvent vapor or solvent steam.4. The method of claim 1 , further comprising removing a releasable assembly from the second major surface of the filtered nanofiber film prior to placing the second major surface of the filtered nanofiber film on the final substrate.5. The method of claim 4 , wherein the releasable assembly comprises a support film and a nanofiber film coated on at least one ...

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25-01-2018 дата публикации

System and Method for Preparing High-Purity Vanadium Pentoxide Powder

Номер: US20180022616A1
Принадлежит:

The present invention provides a system and method for preparing high-purity vanadium pentoxide powder. Industrial grade vanadium pentoxide is converted to vanadium oxytrichloride by low temperature fluidizing chlorination, wherein chlorinating gas is preheated via heat exchange between fluidizing gas and chlorination flue gas, and an appropriate amount of air is added to enable a part of carbon powder to combust so as to achieve a balanced heat supply during the chlorination, thereby increasing the efficiency of chlorination and ensuring good selectivity in low temperature chlorination. The vanadium oxytrichloride is subjected to purification by rectification, ammonium salt precipitation and fluidized calcination, thereby obtaining high-purity vanadium pentoxide, wherein the ammonia gas produced during calcination is condensed and then recycled for ammonium salt precipitation. The system and method have advantages of favorable adaptability to raw material, less pollution, low energy consumption in production, low operation cost, stable product quality, etc. 1. A system for preparing high-purity vanadium pentoxide powder , comprising a feeding device , a low temperature chlorination fluidized bed , a rectification and purification device , an ammonium salt precipitation device , an ammonium salt feeding device , a calcination fluidized bed , a tail gas washing absorber , an induced draft fan and a chimney;wherein the feeding device comprises an industrial grade vanadium pentoxide hopper, an industrial grade vanadium pentoxide screw feeder, a carbon powder hopper and a carbon powder screw feeder;the low temperature chlorination fluidized bed comprises a chlorination bed feeder, a chlorination fluidized bed body, a chlorination bed cyclone separator, a flue gas heat exchanger, a flue gas condenser, a chlorination bed acid-seal tank and a chlorination bed spiral slag-discharging device;the rectification and purification device comprises a distilling still, a rectifying ...

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24-01-2019 дата публикации

Process for producing a metal oxide powder

Номер: US20190023583A1
Принадлежит: Oxford University Innovation Ltd

A process for producing a metal oxide powder comprising: providing a precursor solution or dispersion containing a metal complex; spraying the precursor solution on to a heated substrate in the presence of water, thereby depositing material on the substrate; drying the deposited material; and removing the deposited material from the substrate to produce the metal oxide powder.

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28-01-2016 дата публикации

Cathode active material for secondary battery and method of manufacturing the same

Номер: US20160028076A1
Принадлежит: LG Chem Ltd

Provided are a method of manufacturing a cathode active material including a first step of preparing a metal glycolate solution, a second step of mixing lithium-containing transition metal oxide particles and the metal glycolate solution and stirring in a paste state, a third step of drying the paste-state mixture, and a fourth step of performing a heat treatment on the dried mixture, a cathode active material including a metal oxide layer which is manufactured by the above method, and a secondary battery composed of a cathode including the cathode active material.

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02-02-2017 дата публикации

Methods for producing electrochromic films by low temperature condensation of polyoxometalates

Номер: US20170031224A1

Described are electrochromic films produced by low temperature condensation of polyoxometalates and applications thereof. A method of producing an electrochromic film includes depositing a polyoxometalate (POM) solution on a substrate to form a POM film. The POM solution includes anionic POM clusters and counter ions, and may be doped with near-infrared plasmonic nanocrystals. The film is chemically cured using an acid to condense the POM clusters within the POM film. Another method of producing an electrochromic film includes electrochemical deposition and condensation of POM clusters.

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07-02-2019 дата публикации

VANADIUM OXIDE FILMS AND METHODS OF FABRICATING THE SAME

Номер: US20190040526A1
Принадлежит:

Method for fabricating a crystalline vanadium oxide (VO) film comprising the steps of: a) depositing an amorphous VOfilm on a substrate by pulsed DC magnetron sputtering using a vanadium target, wherein the substrate is exposed to a sputtering gas comprising an inert process gas and oxygen (O), and the substrate has a temperature of less than about 50° C.; and b) annealing the deposited amorphous VOfilm to crystallise the amorphous VOfilm into a crystalline VOfilm that exhibits an insulator-metal transition. The disclosed method for fabricating a crystalline VOfilm may be suitable for a broad range of substrates. 1. A method for fabricating a crystalline vanadium oxide (VO) film comprising the steps of:{'sub': 2', '2, 'a) depositing an amorphous VOfilm on a substrate by pulsed DC magnetron sputtering using a vanadium target, wherein the substrate is exposed to a sputtering gas comprising an inert process gas and oxygen (O), and the substrate has a temperature of less than about 50° C.; and'}{'sub': 2', '2', '2, 'b) annealing the deposited amorphous VOfilm to crystallise the amorphous VOfilm into a crystalline VOfilm that exhibits an insulator-metal transition.'}2. The method according to claim 1 , wherein the annealing is performed at a pressure in the range of about 20 Pa to about 50 Pa.3. The method according to claim 2 , wherein the annealing is performed at a pressure in the range of about 30 Pa to about 40 Pa.4. The method according to claim 1 , wherein the substrate temperature is in the range from about 20° C. to about 30° C.5. The method according to claim 4 , wherein the substrate temperature is about room temperature.6. The method according to claim 1 , wherein the inert process gas is argon (Ar).7. The method according to claim 6 , wherein the sputtering gas has an Omolar concentration in Ar in a range from about 20% to about 60%.8. The method according to claim 7 , wherein the sputtering gas has an Omolar concentration in Ar of about 30%.9. The method ...

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06-02-2020 дата публикации

System for extracting vanadium from leaching solution containing vanadium chromium silicon and for preparing vanadium pentoxide and processing method therefor

Номер: US20200039838A1
Автор: Hongbin CAO, Pengge Ning
Принадлежит: Institute of Process Engineering of CAS

A system for extracting vanadium from a leaching solution containing vanadium chromium silicon and for preparing vanadium pentoxide, and a method therefor, the system comprising, in sequence: an impurity removal system, an extraction system, a reverse-extraction and vanadium precipitation system, a washing system and a calcining system. The method comprises the following steps: removing silicon in a leaching solution by using a silicon removal agent, extracting most of the vanadium to an organic phase by using centrifugal extraction, reverse-extracting the vanadium of a vanadium-rich organic phase by using a mixed solution containing a basic solution and an ammonium salt, and precipitating ammonium metavanadate to obtain an ammonium metavanadate solid, washing and drying, and then calcining at a certain temperature to obtain a low chromium, low silicon, low aluminum and high-purity vanadium pentoxide product.

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16-02-2017 дата публикации

METHOD FOR PRODUCING DISPERSIONS OF NANOSHEETS

Номер: US20170044683A1
Принадлежит:

The present invention provides a method for producing a solution of nanosheets, comprising the step of contacting an intercalated layered material with a polar aprotic solvent to produce a solution of nanosheets, wherein the intercalated layered material is prepared from a layered material selected from the group consisting of a transition metal dichalcogenide, a transition metal monochalcogenide, a transition metal trichalcogenide, a transition metal oxide, a metal halide, an oxychalcogenide, an oxypnictide, an oxyhalide of a transition metal, a trioxide, a perovskite, a niobate, a ruthenate, a layered III-VI semiconductor, black phosphorous and a V-VI layered compound. The invention also provides a solution of nanosheets and a plated material formed from nanosheets. 1. A method for producing a solution of nanosheets , comprising the step of contacting an intercalated layered material with a polar aprotic solvent to produce a solution of nanosheets , wherein the intercalated layered material is prepared from a layered material selected from the group consisting of a transition metal dichalcogenide , a transition metal monochalcogenide , a transition metal trichalcogenide , a transition metal oxide , a metal halide , an oxychalcogenide , an oxypnictide , an oxyhalide of a transition metal , a trioxide , a perovskite , a niobate , a ruthenate , a layered III-VI semiconductor , black phosphorous and a V-VI layered compound.2. The method according to claim 1 , wherein the layered material is selected from the group consisting of a transition metal dichalcogenide claim 1 , a transition metal monochalcogenide claim 1 , a transition metal trichalcogenide claim 1 , a transition metal oxide claim 1 , a layered III-VI semiconductor claim 1 , black phosphorous and a V-VI layered compound.3. The method according to claim 2 , wherein the layered material is selected from the group consisting of a transition metal dichalcogenide claim 2 , a transition metal monochalcogenide ...

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07-02-2019 дата публикации

SYSTEM AND METHOD FOR PREPARING VANADIUM BATTERY HIGH-PURITY ELECTROLYTE

Номер: US20190044171A1
Принадлежит:

A system and method for preparing a vanadium battery high-purity electrolyte, comprising preparing a low-valence vanadium oxide with a valence of 3.5 with liquid phase hydrolysis and fluidization reduction with vanadium oxytrichioride, adding clean water and sulfuric acid for dissolution, and further performing ultraviolet activation to obtain the vanadium electrolyte, for use in an all-vanadium redox flow battery stack. The high-temperature tail gas in the reduction fluidized bed is combusted for preheating the vanadium powder material, to recover the sensible heat and latent heat of the high-temperature tail gas, and the sensible heat of the reduction product is recovered through heat transfer between the reduction product and the fluidized nitrogen gas. An internal member is arranged in the reduction fluidized bed to realize the precise regulation of the valence state of the reduction product, and ultraviolet is used to activate the vanadium ions, improving the activity of the electrolyte. 14. A system for preparing a vanadium battery high-purity electrolyte , comprising a vanadium oxytrichloride storage tank , a liquid phase hydrolysis device , a vanadium pentoxide feeding device , a preheating system () , a reduction fluidized bed , a combustion chamber , a cooling system , a secondary cooling system , a low-valence vanadium oxide feeding device , a dissolution reactor and an activation device;wherein the liquid phase hydrolysis device comprises a liquid phase hydrolysis reaction tank and a washing filter;the vanadium pentoxide feeding device comprises a vanadium pentoxide hopper and a vanadium pentoxide screw feeder;the preheating system comprises a venturi preheater, a primary cyclone preheater, a secondary cyclone preheater and a bag-type dust collector;the reduction fluidized bed comprises a feeder, a bed body, a discharger, a gas heater, a gas purifier and a first cyclone separator;the cooling system comprises a venturi cooler, a cyclone cooler and a ...

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07-02-2019 дата публикации

A SYSTEM AND METHOD FOR PRODUCING HIGH-PURITY AND HIGH-ACTIVITY VANADIUM ELECTROLYTE

Номер: US20190044172A1
Принадлежит:

A system and method for producing a high-purity and high-activity vanadium electrolyte, comprising converting high-purity vanadium oxytrichloride into an ammonium salt in a fluidized bed by gas phase ammoniation, then in another fluidized bed, reducing the ammonium salt into a low-valence vanadium oxide having an average vanadium valence of 3.5, adding clean water and sulfuric acid for dissolution, and further performing activation by ultrasound to obtain a 3.5-valence vanadium electrolyte which can be directly used in a new all-vanadium redox flow battery stack. The method of producing an ammonium salt containing vanadium in the fluidized bed by gas phase ammoniation is of short process and high efficiency. Precise regulation of the valence state of the reduction product is implemented by arranging an internal member in the reduction fluidized bed, and ultrasonication is used to activate the vanadium ion, thereby greatly improving the activity of the electrolyte. 1. A system for producing a high-purity and high-activity vanadium electrolyte , comprising a vanadium oxytrichloride storage tank , a gas phase ammoniation fluidized bed , a reduction fluidized bed , a pre-cooling device , a secondary cooling device , a low-valence vanadium oxide feeding device , a dissolution reactor , and an activation device;wherein the gas phase ammoniation fluidized bed comprises a vanadium oxytrichloride vaporizer, a purified ammonia liquor vaporizer, a chloride spray gun, a gas phase ammoniation fluidized bed body, a first cyclone separator, and an ammonium chloride settling tower;the reduction fluidized bed comprises a material valve, a bed body, a discharger, a gas heater, a gas purifier, and a second cyclone separator;the pre-cooling device comprises a cyclone cooler and a third cyclone separator;the low-valence vanadium oxide feeding device comprises a low-valence vanadium oxide hopper and a low-valence vanadium oxide screw feeder;wherein a feed outlet at the bottom of the ...

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07-02-2019 дата публикации

SYSTEM AND METHOD FOR PRODUCING 3.5-VALENCE HIGH-PURITY VANADIUM ELECTROLYTE

Номер: US20190044173A1
Принадлежит:

A system and method for producing a 3.5-valence high-purity vanadium electrolyte, comprising hydrolyzing high-purity vanadium oxytrichloride into vanadium pentoxide in a fluidized bed, and reducing vanadium pentoxide into a low-valence vanadium oxide having an average vanadium valence of 3.5 adding water and a sulfuric acid solution under a microwave field applied externally for dissolution at a low temperature, to obtain a 3.5-valence high-purity vanadium electrolyte. The preparation of vanadium pentoxide by means of gas-phase hydrolysis in the fluidized bed is of short process and high efficiency. By providing an internal member within the reduction fluidized bed, the precise regulation of the valence state of the reduction product is achieved, and the special chemical effect of the microwave field is used to promote dissolution of the vanadium oxide and activate the vanadium ions, thereby greatly improving the activity of the electrolyte. 1. A system for producing a 3.5-valence high-purity vanadium electrolyte , comprising a vanadium oxytrichloride storage tank , a gas phase hydrolysis fluidized bed , a vanadium pentoxide feeding device , a preheat dedusting device , a reduction fluidized bed , a primary cooling device , a secondary cooling device , a low-valence vanadium oxide feeding device , a dissolution and activation device a tail gas washing absorber , an induced draft fan and a chimney;wherein the gas phase hydrolysis fluidized bed comprises a vanadium oxytrichloride vaporizer, a clean water vaporize, a chloride spray gun a gas phase hydrolysis fluidized bed body, a hydrolysis fluidized bed discharger, and a hydrochloric acid tail gas absorber;the vanadium pentoxide feeding device comprises a vanadium pentoxide hopper and a vanadium pentoxide screw feeder;the preheat dedusting device comprises a venturi preheater, a first cyclone separator, a cyclone preheater, and a bag-type dust collector;the reduction fluidized bed comprises a feeder, a bed body, a ...

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07-02-2019 дата публикации

SYSTEM AND METHOD FOR PREPARING HIGH PURITY VANADIUM ELECTROLYTE

Номер: US20190044174A1
Принадлежит:

A system and method for preparing a high-purity vanadium electrolyte, comprising preparing a low-valence vanadium oxide with vanadium oxytrichloride by ammonium salt precipitation and fluidization reduction, and preparing the high-purity vanadium electrolyte at a low temperature by adding a sulfuric acid solution and clean water under the conditions of ultrasound-assisted dissolution and activation. Efficient utilization of heat is achieved through heat exchange between the ammonium salt and the reduction tail gas and heat exchange between the reduction product and fluidized nitrogen gas. Ammonia gas in the reduction tail gas is recovered for precipitation of vanadium to achieve the recycling of ammonia gas. An internal member is arranged in the reduction fluidized bed to realize the precise regulation of the valence state of the reduction product. Furthermore, ultrasound-assisted dissolution and activation are employed to prepare the vanadium electrolyte at a low temperature, thereby improving the activity of the electrolyte. 1. A system for preparing a high-purity vanadium electrolyte , comprising: a vanadium oxytrichloride storage tank , an ammonium salt precipitating device , an ammonium salt feeding device , a preheating system , a reduction fluidized bed , a cooling system , a secondary cooling device , a low-valence vanadium oxide feeding device , and a dissolution and activation reactor;wherein the ammonium salt precipitating device comprises an ammonium salt precipitating reaction tank and a washing filter;the ammonium salt feeding device comprises an ammonium salt hopper and an ammonium salt screw feeder;the preheating system comprises a primary cyclone preheater, a venturi preheater, a secondary cyclone preheater, and a first cyclone separator;the reduction fluidized bed comprises a feeder, a bed body, a discharger, a gas heater, a gas purifier, and an ammonium chloride settling tower;the cooling system comprises a venturi cooler, a cyclone cooler, and a ...

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03-03-2022 дата публикации

POWDER MATERIAL FOR SINTERING AND SOLID LATENT HEAT STORAGE MEMBER INCLUDING THE SAME

Номер: US20220064510A1

[PROBLEM TO BE SOLVED] To provide a solid heat storage material that is made of a VO-based inorganic material, is easy to sinter, has a high latent heat storage capacity, and can be suitably used as a phase change solid heat storage material, and a method of manufacturing the same. 18.-. (canceled)9. A powder material for sintering ,comprising vanadium and oxygen; and{'sub': '2', 'comprising a vanadium oxide represented by a chemical formula VOand at least one other type of vanadium oxide,'}wherein, when a molar ratio of V and O in all powder is expressed as 1:(2+d), d is in a range of 0 Подробнее

14-02-2019 дата публикации

Metal Oxide Film

Номер: US20190047873A1
Принадлежит: OXFORD UNIVERSITY INNOVATION LIMITED

A process for producing a metal oxide film comprising: providing a precursor solution or dispersion containing a metal complex; spraying the precursor solution on to a heated substrate in the presence of water, thereby depositing material on the substrate; and drying the deposited material, thereby producing the metal oxide film. 1. A process for producing a metal oxide film comprising:providing a precursor solution or dispersion containing a metal complex;spraying the precursor solution on to a heated substrate in the presence of water, thereby depositing material on the substrate; anddrying the deposited material, thereby producing the metal oxide film.2. A process according to claim 1 , wherein the precursor solution is an aqueous solution claim 1 , optionally wherein the concentration of the precursor solution is up to 0.1M.3. (canceled)4. A process according to claim 1 , wherein the metal oxide film comprises claim 1 , or consists essentially of claim 1 , a metal (IV) oxide film (MO claim 1 , where M is a metal) or the metal oxide film comprises claim 1 , or consists essentially of claim 1 , a metal (III) oxide film (MO claim 1 , where M is a metal).5. A process according to claim 1 , wherein the metal is vanadium claim 1 , molybdenum claim 1 , tungsten claim 1 , germanium or manganese claim 1 , optionally wherein the metal is vanadium and the metal complex is vanadyl acetylacetonate claim 1 , or wherein the metal is vanadium and the metal complex is vanadyl oxalate claim 1 , or wherein the metal is molybdenum and the metal complex is molybdenyl acetylacetonate claim 1 , or wherein the metal is molybdenum and the metal complex is molybdenyl oxalate or a suitable molybdenum (IV) complex.6. (canceled)7. (canceled)8. A process according to claim 1 , wherein the oxidation state of the metal is the same in the metal complex as it is in the metal oxide film.9. A process according to claim 1 , wherein the precursor solution comprises one or more further metals as ...

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03-03-2022 дата публикации

VANADIUM OXIDE WITH A FORMULA OF VOx AS CHARGE BALANCING MATERIAL FOR ELECTROCHROMIC DEVICES

Номер: US20220066276A1
Автор: LI XUEFEI, Mei Jianguo
Принадлежит:

An electrochromic device includes a charge balancing thin film comprised of a new vanadium oxide with a formula of VO, which provides a high charge density, low coloration efficiency, an electroactive voltage in close proximity to those of some electrochromic materials, and high chemical and electrochromic stability. Vanadium oxide can be without doping or doped with others. The VOcharge balancing thin film has a porous nanostructure and is amorphous or a combination of amorphous and polycrystalline, and can work with electrochromic conjugated polymer in the device in a minimally color changing mode. A method to design a material for a charge balancing thin film to pair with a working electrode and obtain a low device voltage in an electrochromic device is disclosed. Methods to prepare related charge balancing thin films are also disclosed. 1. An electrochromic device , comprising a charge balancing thin film , the charge balancing thin film including a vanadium oxide with a formula of VO ,wherein:x ranges from 2 to 2.5; and{'sup': 2', '−1', '2, 'a coloration efficiency of the charge balancing thin film is less than about 10 cmC; and a charge density of the charge balancing thin film is greater than about 1 mC/cmat a maximum device working voltage.'}2. The electrochromic device of claim 1 , wherein the vanadium oxide has a porous nanostructure and is amorphous or a combination of amorphous and polycrystalline.3. The electrochromic device of claim 1 , wherein the charge balancing thin film operates in a minimally color changing mode.4. The electrochromic device of claim 1 , wherein the vanadium oxide is a doped VOor a doped VOhydrate.5. The electrochromic device of claim 4 , wherein the doped VOcomprises one or more metal cations of the second to fourth period transition metal on the periodic table.6. The electrochromic device of claim 4 , wherein the doped VOcomprises metal cations selected from one or more of Nb claim 4 , Nb claim 4 , Mo claim 4 , and Mo.7. The ...

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14-02-2019 дата публикации

Oil based product for treating vanadium rich oils

Номер: US20190048278A1
Принадлежит: General Electric Co

Provided are oil-based fuel additive compositions that, when combusted with a fuel containing vanadium in a gas turbine, inhibit vanadium hot corrosion in the gas turbine. The oil-based fuel additive compositions include at least one rare earth element compound or alkaline earth element compound that retards vanadium corrosion resulting from combustion of vanadium rich fuel.

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03-03-2022 дата публикации

REDOX FLOW BATTERY SYSTEMS AND METHODS OF MANUFACTURE AND OPERATION AND REDUCTION OF METALLIC IMPURITIES

Номер: US20220069328A1
Автор: Li Liyu, Wei Kui
Принадлежит:

A redox flow battery system includes an anolyte having a first ionic species in solution; a catholyte having a second ionic species in solution, where the redox flow battery system is configured to reduce the first ionic species in the anolyte and oxidize the second ionic species in the catholyte during charging; a first electrode in contact with the anolyte, where the first electrode includes channels for collection of particles of reduced metallic impurities in the anolyte; a second electrode in contact with the catholyte; and a separator separating the anolyte from the catholyte. A method of reducing metallic impurities in an anolyte of a redox flow battery system includes reducing the metallic impurities in the anolyte; collecting particles of the reduced metallic impurities; and removing the collected particles using a cleaning solution.

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25-02-2021 дата публикации

DOWN-CONVERTED LIGHT EMITTING COMBINATION AND METHOD OF MANUFACTURING THE SAME

Номер: US20210055219A1

A down-converted light emitting combination that generates a visible light when an ultraviolet light is incident is provided. The down-converted light emitting combination includes a first structure made of a first material that generates a visible light of a first color when an ultraviolet light of a first wavelength range is incident and a second structure made of a second material that generates a visible light of a second color different from the first color when the ultraviolet light of a second wavelength range different from the first wavelength range is incident, and the first material and the second material have different emission colors and distributions of intensities of the visible lights generated depending on a wavelength of the incident ultraviolet light. 1. A down-converted light emitting combination comprising:a first structure made of a first material configured to generate a visible light of a first color when an ultraviolet light of a first wavelength range is incident; anda second structure made of a second material configured to generate a visible light of a second color different from the first color when an ultraviolet light of a second wavelength range different from the first wavelength range is incident,wherein the first material and the second material are materials which generate visible lights of different wavelength ranges and different distributions of intensities depending on a wavelength of an incident ultraviolet light.2. The down-converted light emitting combination of claim 1 , further comprising:a substrate for supporting the first structure and the second structure,wherein the first structure and the second structure are formed in a nano-pattern on the substrate, respectively.3. The down-converted light emitting combination of claim 1 , wherein the first material and the second material are provided with yttrium vanadium oxide (YVO) or yttrium oxide (YO) in which lanthanide ions are doped to have down-converted light emission ...

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23-02-2017 дата публикации

ANODE COMPOSITIONS FOR SODIUM-ION BATTERIES AND METHODS OF MAKING SAME

Номер: US20170054176A1
Принадлежит:

A sodium-ion battery includes a cathode comprising sodium; and an anode composition comprising a material having the formula: ABCDO, where A is an alkali metal, alkaline earth metal, or a combination thereof, where B is titanium, C is vanadium, D is one or more transition metal element other than titanium or vanadium, a+b+c+d≦1, a≧0, b+c>0, b≧0, c≧0, d>0, and where the material comprises a ilmenite structure, triclinic VFeOstructure, cubic CaCo(VO)structure, dichromate structure, orthorhombic ∀-CoVOstructure, brannerite structure, thortveitite structure, orthorhombic ∃-CrPOstructure, or the pseudo rutile structure. 2. The sodium-ion battery of claim 1 , wherein (b+c)/d≧1.3. The sodium-ion battery of claim 1 , wherein b=0.4. The sodium-ion battery of claim 1 , wherein c=0.5. The sodium-ion battery of claim 1 , wherein b>0 and c>0.6. The sodium-ion battery according to claim 1 , wherein a>0.05.7. The sodium-ion battery according to claim 1 , wherein D is iron claim 1 , nickel claim 1 , cobalt claim 1 , manganese claim 1 , chromium claim 1 , or combinations thereof.9. The sodium-ion battery according to claim 8 , wherein A or A′ is sodium claim 8 , lithium claim 8 , magnesium claim 8 , calcium claim 8 , or combinations thereof.10. The sodium-ion battery according to claim 8 , wherein the sodium-ion battery further comprises an electrolyte comprising sodium.11. An electronic device comprising a sodium-ion battery according to .12. A method of making a sodium-ion battery claim 8 , the method comprising:providing a cathode comprising sodium;providing an anode comprising vanadium, titanium or a combination thereof, and optionally an alkali metal or alkaline earth metal and optionally a transition metal other than titanium or vanadium; andincorporating the cathode and anode into a battery comprising an electrolyte, wherein the electrolyte comprises sodium. The present disclosure relates to compositions useful as anodes for sodium-ion batteries and methods for preparing and ...

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03-03-2016 дата публикации

Method for processing vanadium-titanium magnetite finished ores by using wet process

Номер: US20160060728A1
Принадлежит: Institute of Process Engineering of CAS

A method for processing vanadium-titanium magnetite finished ores by using a wet process. The method comprises the steps: extracting vanadium from vanadium-titanium magnetite finished ores and processing, by using the vanadium extraction method, obtained leaching residue by using a wet process, so as to obtain titanium; and calcining the remaining liquid extracted during the vanadium extraction, so as to prepare ferric oxide. The flow of the method is short, and the energy consumption is low, thereby avoiding waste of a titanium resource.

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04-03-2021 дата публикации

METHOD FOR PREPARING VANADIUM BATTERY ELECTROLYTE BY USING WASTE VANADIUM CATALYST

Номер: US20210061672A1
Автор: TIAN Xingjiang, XU Xiaodi

The present invention discloses a method for preparing a vanadium battery electrolyte by using a waste vanadium catalyst. The method includes step A: soaking a waste vanadium catalyst in an oxalic acid solution for 2-8 h, to generate a solution containing vanadyl oxalate; step B: cleaning the waste vanadium catalyst, and collecting the vanadyl oxalate solution; and step C: adding a polyacid ester into the vanadyl oxalate solution; and after full reaction, removing impurities by filtration, and concentrating the filtrate to obtain a vanadyl oxalate mother solution. The method for preparing a vanadium battery electrolyte by using a waste vanadium catalyst according to the present invention does not generate wastes which cause environmental pollution in the treatment process, and can make a solution in the waste vanadium catalyst treatment process generate the electrolyte for preparing a vanadium battery. The process is simple and the treatment cost is low. 1. A method for preparing a vanadium battery electrolyte by using a waste vanadium catalyst , comprising the following steps:step A: soaking a waste vanadium catalyst in an oxalic acid solution for 2-8 h, to generate a solution containing vanadyl oxalate;step B: cleaning the waste vanadium catalyst, and collecting the vanadyl oxalate solution;step C: adding a polyacid ester into the vanadyl oxalate solution; and after full reaction, removing impurities by filtration, and concentrating the filtrate to obtain a vanadyl oxalate mother solution; andstep D: adding a sulfuric acid solution into the vanadyl oxalate mother solution to form a vanadyl sulfate solution, and after filtering, obtaining a vanadium electrolyte for preparing a vanadium battery.2. The method for preparing a vanadium battery electrolyte by using a waste vanadium catalyst according to claim 1 , whereinin the step C, a waste vanadium catalyst is further added to the vanadyl oxalate solution, and dried at 80-100° C. to obtain waste vanadium catalyst ...

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21-02-2019 дата публикации

POLYMER SOLUTION ELECTROLYTES

Номер: US20190058214A1
Автор: Tamirisa Prabhakar A.
Принадлежит:

Liquid electrolyte compositions containing a lithium salt, one or more solvents having a boiling point of at least 200° C. and a solubilized polymer are disclosed. Coin cells and laminated foil pack cells containing such liquid electrolyte compositions are also disclosed. 1. A electrolyte composition containing a solubilized polymer comprising:a liquid solution resulting from the combination ofa lithium salt;a solvent or a mixture of solvents having a boiling point of at least 200° C.; anda polymer that is soluble in the electrolyte composition in an amount of from 2 to 25 weight percent based on the total weight of the electrolyte composition.2. The electrolyte composition of wherein the polymer is selected from the group consisting of: polyethylene oxide claim 1 , poly(ethylene-co-propylene oxide) claim 1 , poly (methyl methacrylate) claim 1 , poly(lithium acrylate) claim 1 , poly(butyl acrylate) claim 1 , poly(butyl methacrylate) claim 1 , methyl cellulose claim 1 , hydroxypropyl methyl cellulose claim 1 , cellulose acetate claim 1 , and mixtures thereof.3. The electrolyte composition of wherein the solvent or mixture of solvents having a boiling point of at least 200° C. is selected from the group consisting of propylene carbonate claim 1 , ethylene carbonate claim 1 , dimethoxyethane claim 1 , Gamma butyrolactone claim 1 , dimethylacetamide claim 1 , N-methylpyrrolidone claim 1 , tetraethylene glycol dimethyl ether and mixtures thereof.4. The electrolyte composition of wherein the lithium salt is selected from the group consisting of: lithium bis(trifluoromethylsulfonyl) imide (LiTFSI) claim 1 , lithium bis(fluorosulfonyl)imide (LiFSI)lithium bis(pentafluoroethylsulfonyl) imide (LiBETI) claim 1 , lithium tris(trifluorosulfonyl) methide claim 1 , lithium perchlorate (LiClO) claim 1 , lithium tetrafluoroborate (LiBF) claim 1 , lithium hexafluoroarsenate (LiAsF) claim 1 , lithium hexafluorophosphate (LiPF) claim 1 , Lithium bis(oxalatoborate) (LiBOB) claim 1 , ...

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27-02-2020 дата публикации

Method for Reducing the Bandgap of Titanium Dioxide

Номер: US20200062610A1
Автор: Hisao Yamada
Принадлежит: Individual

This invention describes a new method for reducing the bandgap of titanium dioxide by forming solid solutions with other dioxides that a) have either rutile or anatase crystal structure, b) exhibit either metallic or semiconducting characteristics and c) maintain stable 4+ valence during high temperature processing as well as during cooling to room temperature.

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08-03-2018 дата публикации

VANADIUM-DIOXIDE-CONTAINING PARTICLES HAVING THERMOCHROMIC PROPERTIES AND METHOD FOR PRODUCING THE SAME

Номер: US20180065861A1
Автор: Washizu Takashi
Принадлежит:

By vanadium-dioxide-containing particles having thermochromic properties and configured such that in an X-ray diffraction spectrum using CuKα as the radiation source, the area of a VOmonoclinic peak appearing at 2θ=28°±0.5° and the area of a peak appearing at 2θ=30°±0.5° satisfy a predetermined relation, vanadium-dioxide-containing particles having excellent thermochromic properties are provided. 1. Vanadium-dioxide-containing particles having thermochromic properties , configured such that in an X-ray diffraction spectrum using CuKα as the radiation source , the area of a VOmonoclinic peak appearing at 2θ=28°±0.5° and the area of a peak appearing at 2θ=30°±0.5° satisfy the relation of the following Equation 1:{'br': None, 'i': P', '/P, 'sub': 2', '1, '0.03≦()≦0.2 \u2003\u2003Equation (1)'}{'sub': 1', '2', '2, 'wherein Pis the area of a VOmonoclinic peak appearing at 2θ=28°±0.5°, and Pis the area of a peak appearing at 2θ=30°±0.5°.'}2. The vanadium-dioxide-containing particles according to claim 1 , wherein the particle size at which the cumulative abundance ratio from the small-size side based on the average number of particles by a laser diffraction particle size distribution method is 80% is 150 nm or less.3. A dispersion comprising the vanadium-dioxide-containing particles according to .4. A heat shield film comprising:a substrate; and{'claim-ref': {'@idref': 'CLM-00001', 'claim 1'}, 'an optical functional layer containing the vanadium-dioxide-containing particles according to and a resin.'}5. A method for producing vanadium-dioxide-containing particles having thermochromic properties claim 1 ,the method comprising subjecting a reaction mixture containing a vanadium compound and water to a hydrothermal reaction, thereby forming vanadium-dioxide-containing particles,the temperature rise rate in the hydrothermal reaction being 15 to 80 (°C./h).6. The method according to claim 5 , wherein the temperature of the hydrothermal reaction is 200° C. or more and 350° C. ...

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11-03-2021 дата публикации

SEEDED SOLID-PHASE CRYSTALLIZATION OF TRANSPARENT CONDUCTING VANADATE PEROVSKITES

Номер: US20210069999A1
Принадлежит:

Transparent, electrically conductive vanadium oxide-based perovskite films and methods of making the vanadium oxide-based perovskite films are provided. Transparent conducting vanadate perovskites are made by forming a layer of amorphous vanadate perovskite precursor around a plurality of nanoscale, crystalline, perovskite oxide seeds and heating the layer of amorphous vanadate perovskite precursor at a temperature that favors lateral vanadate perovskite crystal growth from the perovskite oxide seeds over homogeneous crystal nucleation within the layer of amorphous vanadate perovskite precursor material. The crystallization processes can form the desired vanadate perovskite phase directly or via a transformation in a controlled gas environment from an initial crystallized vanadate perovskite phase that has a higher oxidation state. 1. A method of forming a polycrystalline vanadate perovskite film , the method comprising:forming a plurality of nanoscale crystalline perovskite oxide seeds on a substrate;depositing a layer of amorphous vanadate perovskite precursor over the nanoscale crystalline perovskite oxide seeds; andheating the layer of amorphous vanadate perovskite precursor, whereby the layer of amorphous vanadate perovskite precursor is laterally crystallized from the nanoscale crystalline perovskite oxide seeds to form the polycrystalline vanadate perovskite film.2. The method of claim 1 , wherein the polycrystalline vanadate perovskite film comprises SrVO claim 1 , CaVO claim 1 , LaSrVO claim 1 , where x is in the range from 0 to 0.5 claim 1 , or a mixture of two or more thereof.3. The method of claim 1 , wherein the polycrystalline vanadate perovskite film is an SrVOfilm.4. The method of claim 1 , wherein the polycrystalline vanadate perovskite film is a CaVOfilm.5. The method of claim 1 , wherein the polycrystalline vanadate perovskite film is an LaSrVOfilm claim 1 , where x is in the range from 0 to 0.5.6. The method of claim 1 , wherein heating the layer ...

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28-02-2019 дата публикации

68Ge/68Ga Generator

Номер: US20190066860A1
Принадлежит:

A Ge/Ga generator for a continuous production of a Ga daughter nuclide, wherein the Ge parent nuclide thereof is specifically adsorbed to an inorganic support material and wherein said Ge parent nuclide continuously decays to Ga by electron capture at a half-life of 270.82 d, wherein the inorganic support material is at least one oxide of a metal being selected from the group consisting of: Vanadium, Niobium and Tantalum. The use of at least one oxide of a metal being selected from the group consisting of: Vanadium, Niobium and Tantalum as an inorganic support material for the manufacture of a Ge/Ga generator for pharmaceutical purposes. With the inorganic support material of the present invention, it is possible to load Ge/Ga generators with up to 8000 MBq of Ge (corresponding to 80 μg Germanium). 118-. (canceled)19. A Ge/Ga generator for a continuous production of a Ga daughter nuclide , wherein the Ge parent nuclide thereof is specifically adsorbed to an inorganic support material and wherein said Ge parent nuclide continuously decays to Ga by electron capture at a half-life of 270.82 d ,characterized in thatthe inorganic support material is at least one oxide of a metal being selected from the group consisting of Vanadium, Niobium and Tantalum.20. The generator according to claim 19 , characterized in that the oxide is an oxide having the general formula (1):{'br': None, 'sub': 2', '5, 'MO\u2003\u2003(1),'}wherein M is selected from the group consisting of Vanadium, Niobium and Tantalum.21. The generator according to claim 19 , characterized in that the oxide is tantalum pentaoxide (TaO).22. The generator according to claim 21 , characterized in that said TaOis present in its alpha- and/or beta-crystalline form.23. The generator according to claim 19 , characterized in that the oxide is obtainable by hydrolyzing a metal halogenide of the general formula (2):{'br': None, 'sub': '5', 'MX\u2003\u2003(2),'}wherein M is selected from the group consisting of Vanadium, ...

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28-02-2019 дата публикации

Continuous Process for Producing Electrochemical Cells

Номер: US20190067732A1
Автор: Jang Bor Z., Zhamu Aruna
Принадлежит: Nanotek Instruments, Inc.

A process for producing an electrochemical cell, comprising: (A) continuously depositing a wet cathode active material mixture onto a surface of a cathode current collector to form a cathode electrode, wherein the wet cathode active material mixture contains 30% to 85% by volume of a cathode active material and 0% to 15% by volume of a conductive additive dispersed in a first liquid or polymer gel electrolyte; (B) continuously depositing a wet anode active material mixture onto a surface of an anode current collector to form an anode electrode, wherein the wet anode active material mixture contains an anode active material and a conductive additive dispersed in a second electrolytes; and (C) combining the cathode electrode or a portion thereof and the anode electrode or a portion thereof to form the cell; wherein the anode electrode and/or the cathode electrode has a thickness from 200 μm to 3,000 μm. 1. A process for producing an electrochemical cell , said process comprising:(A) continuously depositing a wet cathode active material mixture onto at least a surface of a cathode current collector to form a wet cathode electrode, wherein said wet cathode active material mixture contains 30% to 85% by volume of a cathode active material and 0% to 15% by volume of a conductive additive dispersed in a first liquid or polymer gel electrolyte;(B) continuously depositing a wet anode active material mixture onto at least a surface of an anode current collector to form a wet anode electrode, wherein said wet anode active material mixture contains 30% to 85% by weight of an anode active material and 0% to 15% by volume of a conductive additive dispersed in a second liquid or polymer gel electrolytes; and(C) combining said wet cathode electrode or a portion thereof and said wet anode electrode or a portion thereof to form said electrochemical cell;wherein said anode electrode and/or said cathode electrode has a thickness from 200 μm to 3,000 μm.2. The process of claim 1 , ...

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19-03-2015 дата публикации

METHOD FOR PROCESSING ORGANIC PHASE SUBSTANCE BY USING HALOGEN-CONTAINING CHECICAL OR CHEMICALS AND/OR MIXTURE CONTAINING OXYGEN-CONTAINING OXIDIZER OR OXIDIZERS AND ORGANIC CARBONYL ANALOGUE OR ANALOGUES, AND/OR METHOD FOR EXTRACTING OR DEPOSITING HEAVY ELEMENT SPECIES AND/OR ORGANIC COMPONENTS OF ASPHALTENE AND/OR INORGANIC SUBSTANCE FROM THE ORGANIC PHASE SUBSTANCE BY USING HALOGEN-CONTAINING CHEMICAL OR CHEMICALS AND/OR MIXTURE CONTAINING OXYGEN-CONTAINING OXIDIZER OR OXIDIZERS AND ORGANIC CARBONYL ANALOGUE OR ANALOGUES, AND PLANT USING FOR THE METHOD, AND ORGANIC PHASE SUBSTANCE

Номер: US20150075065A1

The invention provides a processing method for upgrading an organic phase substance by removing heavy element species from the organic phase substance originating from a resource substance in mild environmental conditions, and further provides a method for collecting removed heavy element species and a method for collecting other substances. 1. A method for processing an organic phase substance , comprising:allowing an organic phase substance to coexist with a water phase, wherein the organic phase substance contains at least organic components originating from one or more selected from crude oil, bitumen, tar, residual fuel oil, petroleum residue, oil sands, tar-sand, asphaltene, fossil strata, cokes, oil-shale and coal, and contacting resultant of the above coexistence with halogen-containing chemical or chemicals, thereby extracting or depositing the heavy element species from the organic phase substance into the water phase.2. The method for processing an organic phase substance according to claim 1 , wherein the halogen-containing chemical or chemicals include at least one chlorine-containing chemical or more chlorine-containing chemicals selected from chlorine gas claim 1 , chlorofluorides or an interhalogen compound selected from bromine monochloride or iodine monochloride claim 1 , a chlorine radial and a chlorine oxide.3. The method for processing an organic phase substance according to claim 1 , wherein the halogen-containing chemical or chemicals include at least one bromine-containing chemical or more bromine-containing chemicals selected from bromine gas claim 1 , bromine liquid claim 1 , bromine-containing interhalogen compounds claim 1 , bromine radicals and bromine oxides.4. A method for processing an organic phase substance claim 1 , comprising:allowing an organic phase substance to coexist with a water phase, wherein the organic phase substance contains at least organic components originating from one or more selected from crude oil, bitumen, tar, ...

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07-03-2019 дата публикации

VANADIUM OXIDE FOR INFRARED COATINGS AND METHODS THEREOF

Номер: US20190071319A1
Принадлежит:

The present invention relates to vanadium oxide and methods of controlling reaction processes for making such materials (e.g., powders). In particular embodiments, the method includes control of oxygen partial pressure in order to kinetically control the oxidation species of the crystalline vanadium oxide material. Other methods, uses, systems, protocols, and coatings are also described. 1. A method of preparing crystalline vanadium oxide , the method comprising:(i) providing a vanadium oxide precursor;{'sub': '2', '(ii) annealing the precursor at a reduced Opartial pressure, thereby preparing the crystalline vanadium oxide in tetragonal form; and'}{'sub': 1', '2', '2, '(iii) determining a first temperature Tat which a metastable VOform and/or a tetragonal VOform is present.'}2. The method of claim 1 , further comprising (iv) adjusting to a further reduced Opartial pressure claim 1 , thereby further isolating the crystalline vanadium oxide in tetragonal form.3. The method of claim 1 , wherein the crystalline vanadium oxide is VO.4. The method of claim 1 , wherein the vanadium oxide precursor comprises vanadium oxide particles.5. The method of claim 4 , wherein the crystalline vanadium oxide has substantially the same morphology as the vanadium oxide particles.6. The method of claim 5 , wherein the vanadium oxide particles comprise vanadium pentoxide VO.7. A method of preparing crystalline vanadium oxide claim 5 , the method comprising:(i) providing a vanadium oxide precursor;{'sub': 2', '1, '(ii) annealing the precursor at a first Opartial pressure P, thereby forming one or more vanadium oxide form(s);'}(iii) obtaining one or more spectroscopy measurements of the vanadium oxide form(s);{'sub': 1', '2', '2, '(iv) determining a first temperature Tat which a metastable VOform and/or a tetragonal VOform is present; and'}{'sub': 2', '2', '1, '(v) adjusting to a second Opartial pressure Pwhile maintaining T, thereby preparing the crystalline vanadium oxide.'}8. The method ...

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05-03-2020 дата публикации

PRODUCTION OF ETHYLENE WITH NANOWIRE CATALYSTS

Номер: US20200070136A1
Принадлежит:

Nanowires useful as heterogeneous catalysts are provided. The nanowires catalysts are useful in a variety of catalytic reactions, for example, the oxidative coupling of methane to ethylene. Related methods for use and manufacture of the same are also disclosed. 1. A catalyst comprising an inorganic catalytic nanowire , the nanowire having a ratio of effective length to actual length of less than one and an aspect ratio of greater than ten as measured by TEM in bright field mode at 5 keV , wherein the nanowire comprises one or more elements from any of Groups 1 through 7 , lanthanides , actinides or combinations thereof , wherein the catalyst has a catalytic activity effective to catalyze the oxidative coupling of methane with a Cselectivity of greater than 30% at a temperature below 600° C.2. The catalyst of claim 1 , wherein the one or more elements are in the form of oxides claim 1 , hydroxides claim 1 , oxyhydroxides claim 1 , sulfates claim 1 , carbonates claim 1 , oxide carbonates claim 1 , oxalates claim 1 , phosphates claim 1 , hydrogenphosphates claim 1 , dihydrogenphosphates claim 1 , oxyhalides claim 1 , hydroxihalides claim 1 , oxysulfates or combinations thereof.3. The catalyst of claim 2 , wherein the one or more elements are in the form of oxides.4. The catalyst of claim 2 , wherein the one or more elements are in the form of hydroxides.5. The catalyst of claim 1 , wherein the nanowire comprises Mg claim 1 , Ca claim 1 , La claim 1 , W claim 1 , Mn claim 1 , Mo claim 1 , Nd claim 1 , Sm claim 1 , Eu claim 1 , Pr claim 1 , Zr or combinations thereof.6. The catalyst of claim 1 , wherein the nanowire comprises MgO claim 1 , CaO claim 1 , LaO claim 1 , NaWO claim 1 , MnO claim 1 , MnO claim 1 , NdO claim 1 , SmO claim 1 , EuO claim 1 , PrO claim 1 , MgMnO claim 1 , NaMnO claim 1 , Na/Mn/W/O claim 1 , MnWOor combinations thereof.7. The catalyst of claim 1 , wherein the nanowire further comprises one or more dopants comprising metal elements claim 1 , semi- ...

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18-03-2021 дата публикации

ELECTRODE MATERIALS FOR GROUP II CATION-BASED BATTERIES

Номер: US20210083261A1
Принадлежит:

Preparation, characterization, and an electrochemical study of MgVOprepared by a novel sol-gel method with no high-temperature post-processing are disclosed. Cyclic voltammetry showed the material to be quasi-reversible, with improved kinetics in an acetonitrile-, relative to a carbonate-, based electrolyte. Galvanostatic test data under a C/10 discharge showed a delivered capacity >250 mAh/g over several cycles. Based on these results, a magnesium anode battery, as disclosed, would yield an average operating voltage ˜3.2 Volts with an energy density ˜800 mWh/g for the cathode material, making the newly synthesized material a viable cathode material for secondary magnesium batteries. 1. A composition of matter comprising a compound according to the formula:{'br': None, 'sub': z', 'x', 'y, 'MgMO,'}wherein M is a metal chosen from the group consisting of V, Mn, and Fe;wherein z/(x+y+z) is the mole fraction of Mg in the compound;wherein x/(x±y±z) is the mole fraction of metal M in the compound;wherein y/(x+y+z) is the mole fraction of 0 in the compound; andwherein x and y and z are each greater than zero.2. The composition of claim 1 , wherein:M comprises V; andx=2, and y=5.3. The composition of claim 2 , wherein 0.1 Подробнее

12-05-2022 дата публикации

Electrochemical-Based Purification of Electrolyte Solutions, and Related Systems and Methods

Номер: US20220149405A1
Автор: Sullivan Joseph T.
Принадлежит:

Methods and systems for removing impurities from electrolyte solutions having three or more valence states. In some embodiments, a method includes electrochemically reducing an electrolyte solution to lower its valence state to a level that causes impurities to precipitate out of the electrolyte solution and then filtering the precipitate(s) out of the electrolyte solution. In embodiments in which the electrolyte solution is desired to be at a valence state higher than the precipitation valence state, a method of the disclosure includes oxidizing the purified electrolyte solution to the target valence. 1. A method of commissioning a redox flow battery having a positive side and a negative side , the method comprising:providing an electrolyte solution having an initial valence and at least four available oxidation states comprising a set of higher oxidation states and a set of lower oxidation states;reducing the electrolyte solution to a valence below the initial valence to make a reduced electrolyte solution having a valence within the set of lower oxidation states;oxidizing a first portion of the reduced electrolyte solution to make a positive-side electrolyte solution having a valence within the set of higher oxidation states;providing, for the commissioning, the positive-side electrolyte solution for the positive side of the redox flow battery; andproviding, for the negative side of the redox flow battery for the commissioning, a second portion of the reduced electrolyte solution as a negative-side electrolyte solution having a valence within the set of lower oxidation states.2. The method according to claim 1 , wherein the providing of the second portion of the reduced electrolyte solution as the negative-side solution includes oxidizing the second portion to raise the valence of the second portion to a value within the set of lower oxidation states.3. The method according to claim 1 , further comprising adding the positive-side electrolyte solution to the ...

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28-03-2019 дата публикации

ANNEALING METHOD AND NITROGEN-DOPED METAL OXIDE STRUCTURE

Номер: US20190097227A1

An annealing method is provided. The annealing method includes preparing a metal oxide structure, annealing the metal oxide structure in a gas atmosphere including nitrogen to fabricate a metal compound structure, an oxygen content of which is lower than that of the metal oxide structure, from the metal oxide structure, and annealing the metal compound structure in a gas atmosphere including oxygen to fabricate a nitrogen-doped metal oxide structure, which has a specific surface area greater than that of the metal oxide structure, from the metal compound structure. 1. An annealing method comprising:preparing a metal oxide structure;annealing the metal oxide structure in a gas atmosphere including nitrogen to fabricate a metal compound structure, an oxygen content of which is lower than that of the metal oxide structure, from the metal oxide structure; andannealing the metal compound structure in a gas atmosphere including oxygen to fabricate a nitrogen-doped metal oxide structure, which has a specific surface area greater than that of the metal oxide structure, from the metal compound structure.2. The annealing method of claim 1 , wherein a grain size of the nitrogen-doped metal oxide structure is less than a grain size of the metal oxide structure.3. The annealing method of claim 2 , wherein a grain size of the metal compound structure is less than the grain size of the metal oxide structure claim 2 , andwherein a specific surface area of the metal compound structure is greater than the specific surface area of the metal oxide structure.4. The annealing method of claim 3 , wherein the grain size of the nitrogen-doped metal oxide structure is less than the grain size of the metal compound structure; andwherein the specific surface area of the nitrogen-doped metal oxide structure is less than the specific surface area of the metal compound structure.5. The annealing method of claim 1 , wherein the metal oxide structure is a bulk type claim 1 , andwherein the nitrogen ...

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12-04-2018 дата публикации

Copper Vanadium Oxides as a Reversible Cathode for Lithium Ion Batteries

Номер: US20180102538A1

A lithium ion battery having a cathode including an α-copper vanadium oxide having a stoichiometry of Cu 7−x V 6 O 19−X , wherein 0≤x≤0.5, and a discharge capacity of at least 250 mAh/g after 20 cycles is claimed. Solid state and hydrothermal reaction methods of synthesizing the α-copper vanadium oxide are also claimed.

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12-04-2018 дата публикации

Electrochemical-Based Purification of Electrolyte Solutions, and Related Systems and Methods

Номер: US20180102561A1
Автор: Joseph T. Sullivan
Принадлежит: Vionx Energy Corp

Methods and systems for removing impurities from electrolyte solutions having three or more valence states. In some embodiments, a method includes electrochemically reducing an electrolyte solution to lower its valence state to a level that causes impurities to precipitate out of the electrolyte solution and then filtering the precipitate(s) out of the electrolyte solution. In embodiments in which the electrolyte solution is desired to be at a valence state higher than the precipitation valence state, a method of the disclosure includes oxidizing the purified electrolyte solution to the target valence.

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19-04-2018 дата публикации

METHOD OF TREATING LIQUID ELECTROLYTE SOLUTION

Номер: US20180105944A1
Автор: Smeltz Andrew
Принадлежит:

A method for treating a liquid redox electrolyte solution for use in a flow battery includes feeding a liquid redox electrolyte solution into a first half-cell of an electrochemical cell and feeding a gaseous reductant into a second half-cell of the electrochemical cell, and electrochemically reducing at least a portion of the liquid redox electrolyte solution in the electrochemical cell using the gaseous reductant. 1. A method for treating a liquid electrolyte solution for use in a flow battery , comprising:(a) feeding a liquid redox electrolyte solution into a first half-cell of an electrochemical cell and feeding a gaseous reductant into a second half-cell of the electrochemical cell; and(b) electrochemically reducing at least a portion of the liquid redox electrolyte solution in the electrochemical cell using the gaseous reductant.2. The method as recited in claim 1 , wherein the liquid redox electrolyte solution initially is vanadium(IV) electrolyte solution claim 1 , and the reduced portion of the liquid redox electrolyte solution is vanadium(III) electrolyte solution.3. The method as recited in claim 1 , wherein the gaseous reductant in said step (b) is a hydrogen-containing gas.4. The method as recited in claim 1 , wherein said step (b) includes using hydrogen as the gaseous reductant to electrochemically reduce substantially all of the liquid redox electrolyte solution from vanadium(IV) electrolyte solution to vanadium(III) electrolyte solution.5. The method as recited in claim 1 , wherein said step (b) includes using the gaseous reductant to electrochemically reduce a portion the liquid redox electrolyte solution such that upon completion of said step (b) there is a mixture of ionic species in the liquid redox electrolyte solution.6. The method as recited in claim 5 , wherein the mixture has approximately equimolar amounts of the ionic species.7. The method as recited in claim 5 , further comprising feeding approximately half of the volume of the mixture ...

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28-04-2016 дата публикации

USE OF VANADIUM-CONTAINING PARTICLES AS A BIOCIDE

Номер: US20160113283A1
Принадлежит:

The present invention relates to the use of vanadium-containing particles as a biocide, in particular to the use of vanadium-containing particles comprising at least one vanadium compound and a support material or of a support material in which some metal atoms from the crystal lattice have been replaced by vanadium. Furthermore, it relates to method for preventing biofouling of a substrate and to a method of imparting biocidal properties to the surface of a substrate. 114.-. (canceled)15. A biocide which comprises vanadium-containing particles.16. The biocide according to claim 15 , wherein the vanadium-containing particles are not pure vanadium pentoxide particles.17. The biocide according to claim 15 , wherein the vanadium-containing particles comprise at least one vanadium compound and a support material.18. The biocide according to claim 15 , wherein the vanadium-containing particles comprise a support material in which some metal atoms of the crystal lattice have been replaced by vanadium.19. A process for the prevention of growth of microorganisms which comprises utilizing the biocide as claimed in .20. A process for the prevention of biofouling and/or growth of microorganisms which comprises utilizing a support material in which some metal atoms from the crystal lattice have been replaced by vanadium.21. A process for the prevention of growth of bacteria and/or organisms that cause biofouling which comprises utilizing the biocide as claimed in .22. A process for the prevention of growth of bacteria and/or organisms that cause biofouling which comprises utilizing a support material in which some metal atoms from the crystal lattice have been replaced by vanadium.23. The biocide according to claim 15 , wherein together with an oxidizing agent and a halide selected from chloride claim 15 , bromide and iodide.24. The biocide according to claim 23 , wherein the oxidizing agent is hydrogen peroxide.25. The biocide according to claim 17 , wherein the support ...

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19-04-2018 дата публикации

VANADIUM REDOX FLOW BATTERIES

Номер: US20180108931A1
Принадлежит:

A vanadium redox flow battery employs a single electrolyte as a starting material to be placed in equal amounts in the positive and negative electrolyte storage tanks for supporting electrolytes containing zinc and chloride ions. A supporting solution includes chloride ions and zinc ions, and a half-cell solution including vanadium ions based on an aggregate oxidation state around +3.5 is disposed in the supporting solution to form the electrolyte solution for the redox flow battery. With HCl as a supporting electrolyte, as an alternative to conventional sulfuric acid, the use of zinc provides multiple benefits in the preparation of vanadium-based electrolytes. 1. An electrolyte solution for use in a vanadium redox flow cell battery , comprising:a supporting solution containing chloride ions and zinc ions; anda battery electrolyte solution containing vanadium ions.2. The electrolyte solution of claim 1 , wherein:the total concentration of vanadium lies between 2.0 M and 2.75 M in a liquid solution; andthe vanadium is resistant to precipitation of a solid phase from the liquid solution for a duration of at least two weeks at a temperature within the range of −20° C. to +70° C.3. The electrolyte solution of wherein the electrolyte solution is based on an equimolar mixture of V+ and V+ ions.4. The electrolyte solution of wherein the electrolyte solution has an initial oxidation state substantially around +3.5.5. The electrolyte solution of wherein the electrolyte solution defines V as an electroactive species prior to charging or discharging.6. The electrolyte solution of wherein species of vanadium other than V are excluded from the electrolyte solution.7. The electrolyte solution of wherein the electrolyte solution is obtained by the reduction of V by oxalic acid.8. The solution of wherein the electrolyte solution is obtained by the reduction of V by glycerol.9. The solution of wherein the electrolyte solution defines V as an electroactive species prior to charging ...

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26-04-2018 дата публикации

Desulfurization catalyst for hydrocarbon oils, its preparation, and use thereof

Номер: US20180112139A1
Принадлежит:

Disclosed is a desulfurization catalyst for hydrocarbon oils, comprising a support and at least one metal promoter selected from the group consisting of cobalt, nickel, iron and manganese, the support comprising at least one metal oxide selected from the group consisting of oxides of Group IIB, Group VB and Group VIB metals and a refractory inorganic oxide, wherein the support further comprises at least about 5% by weight of vanadium carbide, based on the total weight of the desulfurization catalyst for hydrocarbon oils. The desulfurization catalyst for hydrocarbon oils shows a good stability, a high desulfurization activity, an excellent abrasion resistance, and a long service life. Also disclosed is a process for preparing the desulfurization catalyst for hydrocarbon oils, and use of the catalyst in the desulfurization of sulfur-containing hydrocarbon oils. 1. A desulfurization catalyst for hydrocarbon oils , comprising a support and at least one metal promoter selected from the group consisting of cobalt , nickel , iron and manganese , the support comprising at least one metal oxide selected from the group consisting of oxides of Group IIB , Group VB and Group VIB metals and a refractory inorganic oxide , wherein the support further comprises at least about 5% by weight of vanadium carbide , based on the total weight of the desulfurization catalyst for hydrocarbon oils.2. The desulfurization catalyst for hydrocarbon oils according to claim 1 , wherein the desulfurization catalyst is substantially free of silica.3. The desulfurization catalyst for hydrocarbon oils according to claim 1 , wherein the desulfurization catalyst comprises or consists of:1) about 10-80% by weight of the metal oxide;2) about 3-35% by weight of the refractory inorganic oxide;3) about 5-40% by weight of the vanadium carbide; and4) about 5-30% by weight of the metal promoter,based on the total weight of the desulfurization catalyst for hydrocarbon oils.4. The desulfurization catalyst for ...

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13-05-2021 дата публикации

Preparation method and application of tetragonal NaV2O5H2O nanosheet-like powder

Номер: US20210139343A1
Принадлежит:

A preparation method of a tetragonal NaVO.HO nanosheet-like powder includes steps of: (Step 1) simultaneously adding NaVOand NaS.9HO into deionized water, and then magnetically stirring, and obtaining a black turbid solution; (Step 2) sealing after putting the black turbid solution into an inner lining of a reaction kettle, fixing the sealed inner lining in an outer lining of the reaction kettle, placing the reaction kettle into a homogeneous reactor, and then performing a hydrothermal reaction; and (Step 3) after completing the hydrothermal reaction, naturally cooling the reaction kettle to the room temperature, and then alternately cleaning through water and alcohol, and then collecting a product, drying the product, and finally obtaining the tetragonal NaVO.HO nanosheet-like powder with a thickness in a range of 30-60 nm and a single crystal structure grown along a (002) crystal orientation. 1. A preparation method of a tetragonal NaVO.HO nanosheet-like powder used as an anode material of a lithium ion battery , wherein:{'sub': 2', '5', '2, 'the tetragonal NaVO.HO nanosheet-like powder has a thickness in a range of 30-60 nm and a layer spacing of 7.71 Å, and is a single crystal layered structure grown along a (002) crystal orientation;'}{'sub': 2', '5', '2, 'sup': −1', '−1', '−1', '−1', '−1', '−1', '−1, 'when the tetragonal NaVO.HO nanosheet-like powder acts as the anode material of the lithium ion battery, at a current density of 100, 200, 500, 1000 and 2000 mAg, a capacity reaches 348, 285, 209, 167 and 130 mAhg, respectively; at the current density of 100 and 200 mAg, a first discharge capacity reaches 859 and 633 mAhg, respectively; and after 480 and 600 cycles, the capacity reaches 483 and 320 mAhg, respectively; and after 1000 cycles at the current density of 1000 mAg, the capacity reaches 129 mAhg;'}the preparation method comprises the steps of:{'sub': 3', '2', '2, '(Step 1) simultaneously adding 0.8-1.2 g of NaVOand 0.5-3.5 g of NaS.9HO into 55-65 ml of ...

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07-05-2015 дата публикации

Transparent conductive thin film

Номер: US20150123046A1
Принадлежит: SAMSUNG ELECTRONICS CO LTD

Disclosed is a transparent conductive thin film and an electronic device including the same. The transparent conductive thin film may include a perovskite vanadium oxide represented by Chemical Formula 1, A 1-x VO 3±δ   [Chemical Formula 1] wherein A is a Group II element, 0 ≦x<1, and δ is a number necessary for charge balance in the oxide.

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09-04-2020 дата публикации

POLYMER TEMPLATED NANOWIRE CATALYSTS

Номер: US20200109094A1
Принадлежит:

Nanowires useful as heterogeneous catalysts are provided. The nanowire catalysts are prepared by polymer templated methods and are useful in a variety of catalytic reactions, for example, the oxidative coupling of methane to ethane and/or ethylene. Related methods for use and manufacture of the same are also disclosed. 133.-. (canceled)34. A process for the preparation of ethylene from methane comprising contacting a mixture comprising oxygen and methane with a catalytic material comprising nanowires comprising a plurality of metal oxides (MO) , metal oxy-hydroxides (MOOH) , metal oxycarbonates (MO(CO)) or metal carbonates (M(CO)) or combinations thereof , the nanowires prepared by a method comprising:a) providing a solution comprising a polymer template; and{'sub': m', 'n', 'p, '(b) introducing at least one metal ion and at least one anion to the solution under conditions and for a time sufficient to allow for nucleation and growth of nanowires comprising a plurality of metal salts (MXZ) on the polymer template,'}wherein:M is, at each occurrence, independently a metal element from any of Groups 1 through 7, lanthanides or actinides;X is, at each occurrence, independently hydroxide, carbonate, bicarbonate, phosphate, hydrogenphosphate, dihydrogenphosphate, sulfate, nitrate or oxalate;Z is O;n, m, x and y are each independently a number from 1 to 100; andp is a number from 0 to 100.35. The process of claim 34 , wherein the polymer template is functionalized with at least one of amine claim 34 , carboxylic acid claim 34 , sulfate claim 34 , alcohol or thiol groups.36. The process of claim 35 , wherein the polymer template comprises a hydrocarbon polymer.37. The process of claim 36 , wherein the polymer template comprises polystyrene.38. The process of claim 34 , wherein the method further comprises converting the nanowires comprising the plurality of metal salts (MXZ) to the nanowires comprising the plurality of metal oxides (MO) claim 34 , metal oxy-hydroxides (MOOH) ...

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03-05-2018 дата публикации

PRODUCTION OF ETHYLENE WITH NANOWIRE CATALYSTS

Номер: US20180117579A1
Принадлежит:

Nanowires useful as heterogeneous catalysts are provided. The nanowire catalysts are useful in a variety of catalytic reactions, for example, the oxidative coupling of methane to ethylene. Related methods for use and manufacture of the same are also disclosed. 1113-. (canceled)114. A method for the preparation of ethylene from methane , the method comprising contacting a mixture comprising oxygen and methane at a temperature below 600° C. with a catalytic nanowire , thereby producing C2 hydrocarbons at a selectivity of greater than 30% , wherein the catalytic nanowire comprises one or more elements from any of Groups 1 through 7 , lanthanides , actinides or combinations thereof in the form of oxides , hydroxides , oxyhydroxides , sulfates , carbonates , oxide carbonates , oxalates , phosphates , hydrogenphosphates , dihydrogenphosphates , oxyhalides , hydroxihalides , oxysulfates or combinations thereof.115. The method of claim 114 , wherein the one or more elements are in the form of oxides.116. The method of claim 114 , wherein the catalytic nanowire comprises Mg claim 114 , Ca claim 114 , La claim 114 , W claim 114 , Mn claim 114 , Mo claim 114 , Nd claim 114 , Sm claim 114 , Eu claim 114 , Pr claim 114 , Zr or combinations thereof.117. The method of claim 114 , wherein the catalytic nanowire comprises MgO claim 114 , CaO claim 114 , LaO claim 114 , NaWO claim 114 , MnO claim 114 , MnO claim 114 , NdO claim 114 , SmO claim 114 , EuO claim 114 , PrO claim 114 , MgMnO claim 114 , NaMnO claim 114 , Na/Mn/W/O claim 114 , MnWOor combinations thereof.118. The method of claim 114 , wherein the catalytic nanowire further comprises one or more dopants comprising metal elements claim 114 , semi-metal elements claim 114 , non-metal elements or combinations thereof.119. The method of claim 118 , wherein the dopant comprises Li claim 118 , Na claim 118 , K claim 118 , Mg claim 118 , Ca claim 118 , Ba claim 118 , Sr claim 118 , Eu claim 118 , Sm claim 118 , Co or Mn.120. The ...

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03-05-2018 дата публикации

NANOWIRE CATALYSTS AND METHODS FOR THEIR USE AND PREPARATION

Номер: US20180118637A1
Принадлежит:

Nanowires useful as heterogeneous catalysts are provided. The nanowire catalysts are useful in a variety of catalytic reactions, for example, the oxidative coupling of methane to C2 hydrocarbons. Related methods for use and manufacture of the same are also disclosed. 141-. (canceled)42. A method for the preparation of ethane , ethylene or combinations thereof , the method comprising contacting a catalytic material with a gas comprising methane , wherein the catalytic material comprises a plurality of catalytic nanowires and a diluent or support , the diluent or support comprising an alkaline earth metal compound.43. The method of claim 42 , wherein the catalytic material is in the form of a pressed pellet claim 42 , extrudate or monolith.44. The method of claim 42 , wherein the catalytic material is in the form of a pressed pellet.45. The method of claim 42 , wherein the catalytic material is in the form of an extrudate.46. The method of claim 42 , wherein the catalytic material is in the form of a monolith.47. The method of claim 42 , wherein the catalytic nanowires comprise one or more doping elements.48. The method of claim 42 , wherein the catalytic material is in the form of a pressure treated claim 42 , pressed pellet and comprises substantially no binder material.49. The method of claim 42 , wherein the catalytic material is in the form of a pressed pellet or extrudate and comprises pores greater than 20 nm in diameter.50. The method of claim 42 , wherein the alkaline earth metal compound is an alkaline earth metal oxide claim 42 , alkaline earth metal carbonate claim 42 , alkaline earth metal sulfate or alkaline earth metal phosphate.51. The method of claim 42 , wherein the alkaline earth metal compound is an alkaline earth metal carbonate claim 42 , alkaline earth metal sulfate or alkaline earth metal phosphate.52. The method of claim 42 , wherein the diluent or support comprises MgO claim 42 , MgCO claim 42 , MgSO claim 42 , Mg(PO) claim 42 , MgAlO claim ...

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04-05-2017 дата публикации

Ceramic material

Номер: US20170121229A1
Автор: Sakyo Hirose
Принадлежит: Murata Manufacturing Co Ltd

The present disclosure provides a ceramic material containing a vanadium oxide, and 50 to 400 ppm by mass of nitrogen with respect to the vanadium oxide. The ceramic material according to the present disclosure less varies in the amount of heat absorption. A cooling device comprising the ceramic material is also provided.

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16-04-2020 дата публикации

ONE-DIMENSIONAL NANO-CHAIN STRUCTURE AND PREPARING METHOD THEREOF

Номер: US20200115252A1

The present disclosure relates to a one-dimensional nano-chain structure including a single crystal structure as a minimum repeat unit structure. 1. A one-dimensional nano-chain structure including a single crystal structure as a minimum repeat unit structure.2. The one-dimensional nano-chain structure of claim 1 ,wherein the one-dimensional nano-chain structure does not have a dangling bond on its lateral surfaces.3. The one-dimensional nano-chain structure of claim 1 ,wherein the one-dimensional nano-chain structure has a thickness of 10 nm or less.4. The one-dimensional nano-chain structure of claim 1 ,wherein the minimum repeat unit structure includes an inorganic molecule.5. The one-dimensional nano-chain structure of claim 1 , {'br': None, 'sub': 2', '9, 'MX\u2003\u2003[Chemical Formula 1]'}, 'wherein the minimum repeat unit structure is represented by the following Chemical Formula 1(in the above Chemical Formula 1,M is V, Nb, Ta, or Db, andX is S, Se, Te, or Po).6. The one-dimensional nano-chain structure of claim 1 ,{'sub': 2', '9', '2', '9', '2', '9', '2', '9', '2', '9', '2', '9', '2', '9', '2', '9, 'wherein the one-dimensional nano-chain structure includes a unit structure selected from the group consisting of VSe, NbSe, TaSe, DbSe, VTe, NbTe, TaTe, DbTe, and combinations thereof.'}7. The one-dimensional nano-chain structure of claim 1 ,wherein the one-dimensional nano-chain structure is bonded to each other by a van der Waals force.8. A one-dimensional nanostructure bundle in which one-dimensional nano-chain structures of are bonded by a van der Waals force.9. A preparing method of a one-dimensional nano-chain structure of claim 1 , comprising:separating the one-dimensional nano-chain structure from a one-dimensional single crystal bulk material.10. The preparing method of a one-dimensional nano-chain structure of claim 9 , comprising:dispersing the one-dimensional single crystal bulk material in a solvent;irradiating an ultrasonic wave to the solvent; ...

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03-05-2018 дата публикации

ACTIVE MATERIAL, NONAQUEOUS ELECTROLYTE BATTERY, BATTERY PACK AND BATTERY MODULE

Номер: US20180123127A1
Принадлежит: KABUSHIKI KAISHA TOSHIBA

In general, according to one embodiment, there is provided an active material. The active material contains a composite oxide having an orthorhombic crystal structure. The composite oxide is represented by a general formula of LiNaM1TiM2O. In the general formula, the M1 is at least one selected from the group consisting of Cs and K; the M2 is at least one selected from the group consisting of Zr, Sn, V, Nb, Ta, Mo, W, Fe, Co, Mn, and Al; and w is within a range of 0≤w≤4, x is within a range of 0 Подробнее

01-09-2022 дата публикации

CORE-SHELL STRUCTURE TYPE WAVE ABSORBING MATERIAL, PREPARATION METHOD THEREFOR, AND APPLICATION

Номер: US20220274844A1
Принадлежит:

Disclosed are a core-shell structure type wave absorbing material and a preparation method therefor. The wave absorbing material has a core-shell structure with two-dimensional transition metal-chalcogen compound nanosheets as cores and hollow carbon spheres as shells. The preparation method includes: dissolving the hollow carbon spheres in a solvent, sequentially adding a transition metal source and a chalcogen source, taking a solvothermal reaction after dissolution through stirring, and then performing posttreatment to obtain the wave absorbing material. The present invention further discloses an application of the wave absorbing material in fields of military and civilian high-frequency electromagnetic compatibility and protection. The core-shell structure type wave absorbing material of the present invention has a density of 0.3 to 1.5 g/cm, a maximum reflection loss value and an effective bandwidth of the material can be effectively improved in a frequency range of 2 to 40 GHz, and the core-shell structure type wave absorbing material is an electromagnetic compatibility and protection material capable of meeting requirements of civilian high-frequency electronic devices and military weapons and equipment such as airships and artillery shells. 1. A core-shell structure type wave absorbing material , having a core-shell structure with two-dimensional transition metal-chalcogen compound nanosheets as cores and hollow carbon spheres as shells , whereinthe transition metal is selected from Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Zr, Nb, Mo, Hf, Ta, W and Re, and the chalcogen is selected from S, Se and Te.2. The core-shell structure type wave absorbing material according to claim 1 , wherein a matching thickness of the wave absorbing material in a frequency band of 2 to 40 GHz is 0.5 to 5.0 mm claim 1 , a maximum reflection loss (RL) is −40 to 80 dB claim 1 , and an effective absorption bandwidth with a RL smaller than −10 dB is 2.5 to 12 GHz.3. A preparation method for the ...

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21-05-2015 дата публикации

METHOD FOR THE EXTRACTION OF VANADIUMPENTOXIDE, V2O5, FROM A SOURCE CONTAINING VANADIUM

Номер: US20150139873A1
Принадлежит:

The invention relates to a method for the extraction of vanadium from various sources in the form of vanadiumpentoxide, VO, from a source containing vanadium. The method includes the steps of: providing a source of VO, heating the source to a temperature of at least 1000° C., evaporating VOfrom the heated source and recovering the evaporated VO. 1. A method for the extraction of vanadium pentoxide , VO , from a source containing VO , the method comprises the steps of:providing a source containing vanadium,{'sub': 2', '5', '2', '5, 'if necessary, converting at least part of the vanadium in said source to VO, thereby providing a source of VO,'}{'sub': 2', '5, 'heating the source of VOto a temperature of at least 1000° C.,'}{'sub': 2', '5, 'evaporating VOfrom the heated source and'}{'sub': 2', '5, 'recovering the evaporated VO.'}215-. (canceled)16. The method according to claim 1 , wherein the vanadium containing source is selected from the group of: ore claim 1 , slag claim 1 , ash and vanadium-sulphide.17. The method according to claim 1 , wherein the vanadium containing source is from spent petroleum refining catalysts.18. The method according to claim 16 , wherein the ore is selected from the iron sands claim 16 , magnetite claim 16 , hematite claim 16 , titani-ferrous magnetite and vanadium-titanium magnetite; the slag is selected from converter slag claim 16 , submerged arc furnace slag claim 16 , ladle slag and slag obtained by selective oxidation of vanadium from raw iron; and the ash is selected from petroleum coke ash.19. The method according to claim 16 , wherein the ash is selected from fly ash and boiler ash.20. The method according to claim 1 , wherein the evaporation is carried out by the use of a gas.21. The method according to claim 1 , wherein the evaporation is carried out by the use of air or oxygen enriched air containing 22-99% oxygen.22. The method according to claim 1 , wherein the evaporation is carried out by the use of only oxygen.23. The ...

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17-05-2018 дата публикации

PRODUCTION OF VCl4

Номер: US20180134575A1
Принадлежит:

A process () for the production of VCIincludes suspending a solid particulate oxygen-free vanadium compound starting material in a liquid reaction medium to form a reaction mixture, and reacting the oxygen-free vanadium compound starting material suspended in the liquid reaction medium with a chlorinating agent () to produce liquid VCI. The liquid reaction medium in the reaction mixture is maintained at a reaction temperature above its normal boiling point and the oxygen-free compound starting material and the chlorinating agent are reacted at a reaction pressure higher than the vapour pressure of the liquid reaction medium at the reaction temperature of the process so that the reaction mixture does not boil. 1. A process for the production of VCl , the process includingsuspending a solid particulate oxygen-free vanadium compound starting material in a liquid reaction medium to form a reaction mixture; and{'sub': '4', 'reacting the oxygen-free vanadium compound starting material suspended in the liquid reaction medium with a chlorinating agent to produce liquid VCl, the liquid reaction medium in the reaction mixture being at a reaction temperature above its normal boiling point and the oxygen-free compound starting material and the chlorinating agent being reacted at a reaction pressure higher than the vapour pressure of the liquid reaction medium at the reaction temperature of the process so that the reaction mixture does not boil.'}2. The process as claimed in claim 1 , in which the oxygen-free vanadium compound starting material is selected from the group consisting of vanadium nitride claim 1 , vanadium carbide claim 1 , vanadium carbonitride claim 1 , vanadium silicide claim 1 , ferro vanadium claim 1 , and mixtures of two or more thereof.3. The process as claimed in claim 1 , in which the liquid reaction medium is a fully chlorinated liquid claim 1 , which is not prone to being further chlorinated.4. The process as claimed in claim 1 , in which the liquid ...

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17-05-2018 дата публикации

METHOD FOR PRODUCING VANADIUM COMPOUND, METHOD FOR PRODUCING VANADIUM SOLUTION, AND METHOD FOR PRODUCING REDOX FLOW BATTERY ELECTROLYTE

Номер: US20180135149A1
Автор: HANAWA Kenzo, ORIJI Gaku
Принадлежит: SHOWA DENKO K.K.

This method for producing a vanadium compound has an alkaline leaching step for immersing incineration ash in an alkaline solution to cause vanadium to leach from the incineration ash into the alkaline solution and obtain a leachate slurry, a solid-liquid separation step for separating the leachate slurry obtained in the alkaline leaching step into a solid and liquid followed by removing insoluble matter to obtain a leachate, a pH adjustment step for adding acid to the leachate following solid-liquid separation to make the leachate acidic, an aging step for aging the leachate following pH adjustment until a precipitate forms in the leachate, and a separation step for separating the precipitate from the leachate following the aging step. 1. A method for producing a vanadium compound , comprising:an alkaline leaching step for immersing incineration ash in an alkaline solution to cause vanadium to leach from the incineration ash into the alkaline solution and obtain a leachate slurry,a solid-liquid separation step for separating the leachate slurry obtained in the alkaline leaching step into a solid and liquid followed by removing insoluble matter to obtain a leachate,a pH adjustment step for adding acid to the leachate following solid-liquid separation to make the leachate acidic,an aging step for aging the leachate following pH adjustment until a precipitate forms in the leachate, anda separation step for separating the precipitate from the leachate following the aging step.2. The method for producing a vanadium compound according to claim 1 , wherein the solid-liquid separation is carried out by filtration.3. The method for producing a vanadium compound according to claim 1 , wherein an oxidizing agent is added to the alkaline solution in the alkaline leaching step.4. The method for producing a vanadium compound according to claim 1 , wherein the pH of the alkaline solution following immersion of the incineration ash in the alkaline leaching step is 10 or higher.5. ...

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09-05-2019 дата публикации

Preparation method and application of tetragonal NaV2O5°H2O nanosheet-like powder

Номер: US20190135652A1
Принадлежит:

A preparation method of a tetragonal NaVO.HO nanosheet-like powder includes steps of: (S1) simultaneously adding NaVOand NaS.9HO into deionized water, and then magnetically stirring, and obtaining a black turbid solution; (S2) sealing after putting the black turbid solution into an inner lining of a reaction kettle, fixing the sealed inner lining in an outer lining of the reaction kettle, placing the reaction kettle into a homogeneous reactor, and then performing a hydrothermal reaction; and (S3) after completing the hydrothermal reaction, naturally cooling the reaction kettle to the room temperature, and then alternately cleaning through water and alcohol, and then collecting a product, drying the product, and finally obtaining the tetragonal NaVO.HO nanosheet-like powder with a thickness in a range of 30-60 nm and a single crystal structure grown along a (002) crystal orientation. 1. A preparation method of a tetragonal NaVO.HO nanosheet-like powder , which comprises steps of:{'sub': 3', '2', '2, '(S1) simultaneously adding 0.8-1.2 g of NaVOand 0.5-3.5 g of NaS.9HO into 55-65 ml of deionized water, and then magnetically stirring, and obtaining a black turbid solution;'}(S2) sealing after putting the black turbid solution into an inner lining of a reaction kettle according to a filling ratio in a range of 55-65%, fixing the sealed inner lining in an outer lining of the reaction kettle, placing the reaction kettle into a homogeneous reactor, and then heating under a rotational speed in a range of 5-15 r/min from a room temperature to 150-200° C., and then performing a hydrothermal reaction; and{'sub': 2', '5', '2, '(S3) after completing the hydrothermal reaction, naturally cooling the reaction kettle to the room temperature, and then alternately cleaning through water and alcohol, and then collecting a product, drying the product at 40-80° C., and finally obtaining the tetragonal NaVO.HO nanosheet-like powder.'}2. The preparation method of the tetragonal NaVO.HO ...

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17-05-2018 дата публикации

Battery with enhanced resistance to dendrite formation

Номер: US20180138463A1
Принадлежит: Pacesetter Inc

A battery includes a case having a feedthrough port, a feedthrough assembly disposed in the feedthrough port, and a cell stack disposed within the case. The feedthrough port includes an inner conductor and an insulator core separating the inner conductor from the case. The cell stack includes an anode, a cathode, and a separator insulating the anode from the cathode, wherein the anode and cathode are offset from one another. An insulating boot surrounding the cell stack insulates the cell stack from the case. The insulating boot has an opening configured to receive therein the feedthrough assembly, which may include overmolded insulation. The interior surfaces and interior walls of the battery case may be thermal spray-coated with a dielectric material to prevent lithium dendrite formation between cathode and anode surfaces.

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30-04-2020 дата публикации

THERMOCHROMIC FENESTRATION FILMS CONTAINING VANADIUM DIOXIDE NANOCRYSTALS

Номер: US20200131328A1
Принадлежит:

Vanadium oxide nanomaterial composite compositions and substrates including films comprising vanadium oxide nanomaterial composite compositions are described. A film and composition generally including a polymeric matrix; and a crystalline vanadium oxide nanomaterial dispersed in the polymeric matrix, wherein the crystalline vanadium oxide nanomaterial comprises a smallest dimension between about 100 nm and about 5 nm. 1. A composition comprising:a polymeric matrix; anda crystalline vanadium oxide nanomaterial dispersed in the polymeric matrix, wherein the crystalline vanadium oxide nanomaterial comprises an average smallest dimension between about 100 nm and about 5 nm.2. The composition of claim 1 , wherein the crystalline vanadium oxide nanomaterial has an average smallest dimension chosen from between about 50 nm and about 5 nm claim 1 , about 50 nm and about 10 nm claim 1 , and about 15 nm and about 5 nm.3. The composition of claim 1 , wherein the crystalline vanadium oxide nanomaterial has an average smallest dimension of about 40 nm.4. The composition of claim 1 , wherein the crystalline vanadium oxide nanomaterial is a nanomaterial chosen from a nanoparticle claim 1 , a nanowire claim 1 , a nanorod claim 1 , a nanosphere claim 1 , a nanostar claim 1 , and combinations thereof.5. The composition of claim 1 , wherein the crystalline vanadium oxide nanomaterial has an insulator-metal electronic transition at a temperature between about −20° C. and about 100° C.6. The composition of claim 5 , wherein the insulator-metal electronic transition is accompanied by a modulation of near-infrared (NIR) light transmittance.7. The composition of claim 6 , wherein an integrated modulation of light transmittance between about 680 nm and about 2 claim 6 ,500 nm is between about 5% and about 75%.8. The composition of claim 6 , wherein an onset of modulation of NIR light transmittance occurs between about 680 nm and about 1750 nm.9. The composition of claim 1 , wherein a dried ...

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01-06-2017 дата публикации

PLASMA PROCESSING DETECTION INDICATOR USING INORGANIC SUBSTANCE AS A COLOR-CHANGE LAYER

Номер: US20170153174A1
Принадлежит: SAKURA COLOR PRODUCTS CORPORATION

The present invention provides a plasma treatment detection indicator including a color-changing layer that changes color by plasma treatment, exhibiting excellent heat resistance, with the gasification of the color-changing layer or the scattering of the fine debris of the color-changing layer caused by the plasma treatment being suppressed to such a degree as to not affect the electronic device properties. Specifically, the present invention provides a plasma treatment detection indicator including a color-changing layer that changes color by plasma treatment, the color-changing layer containing at least one metal element selected from the group consisting of Mo, W, Sn, V, Ce, Te, and Bi in the form of a simple substance and/or an inorganic compound containing at least one metal element selected from the group consisting of Mo, W, Sn, V, Ce, Te, and Bi. 1. A plasma treatment detection indicator comprising a color-changing layer that changes color by plasma treatment , the color-changing layer comprising at least one metal element selected from the group consisting of Mo , W , Sn , V , Ce , Te , and Bi in the form of a simple substance and/or an inorganic compound containing at least one metal element selected from the group consisting of Mo , W , Sn , V , Ce , Te , and Bi.2. The plasma treatment detection indicator according to claim 1 , wherein the valence of the at least one metal element contained in the inorganic compound is at least one member selected from the group consisting of Mo(II) to Mo(VI) claim 1 , W(II) to W(VI) claim 1 , Sn(II) claim 1 , Sn(IV) claim 1 , V(II) to V(V) claim 1 , Ce(III) to Ce(IV) claim 1 , Te(II) claim 1 , Te(IV) claim 1 , Te(VI) claim 1 , Bi(III) claim 1 , and Bi(V).3. The plasma treatment detection indicator according to claim 1 , wherein the inorganic compound is at least one member selected from the group consisting of oxides claim 1 , hydroxides claim 1 , carbonates claim 1 , oxide salts claim 1 , oxoacids claim 1 , oxoacid ...

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17-06-2021 дата публикации

ANODE MATERIAL FOR RECHARGEABLE LI-ION BATTERIES

Номер: US20210184210A1
Автор: Liu Haodong, Liu Ping
Принадлежит:

Materials, designs, methods of manufacture, and devices are provided for an anode material for a rechargeable lithium-ion battery. For example, an anode material may include LiVO. 0≤x≤7, 0≤y≤1, and z may be based on the charge resulting from Liand V. Also, a cell can include a lithiated anode material. The lithiated anode material may include Li3±xV2±yO5±z. The lithiated anode material may be casted on a first substrate to form a lithiated anode, having a separator stacked on the lithiated anode. The separator may include electrolytes. A cathode can be stacked on the separator. The cathode being formed by casting a cathode material on a second substrate. 1. An anode material comprising LiVO , wherein 0≤x≤7 , 0≤y≤1 , and z is based on the charge resulting from Liand V.2. The anode material of claim 1 , wherein the LiVOis an omega structure claim 1 , wherein the omega structure is a disordered rocksalt structure in the Fmm space group.3. The anode material of claim 1 , wherein lithium is reversibly inserted to form at least one of LiVOand LiVO.4. The anode material of claim 3 , wherein the LiVOor LiVOis an omega structure claim 3 , wherein the omega structure is a disordered rocksalt structure in the Fmm space group.5. The anode material of claim 1 , further comprising one or more materials selected from the group of silicon claim 1 , tin claim 1 , graphite claim 1 , or non-graphitized carbon claim 1 , wherein the one or more materials are blended with the anode material.6. The anode material of claim 1 , wherein the cathode is selected from the group comprising one or more of one or more of LiMnO claim 1 , LiNiCoMnOwhere x+y+z=1 claim 1 , or other cathodes.7. The anode material of claim 1 , further comprising repeating the above steps to form a pouch-type cell.8. An anode material comprising a composition defined by LiVMO claim 1 , wherein M is a dopant claim 1 , and wherein 0.5 Подробнее

22-09-2022 дата публикации

COMBUSTION ASH HANDLING METHOD AND SYSTEM, AND PETROLEUM-BASED FUEL COMBUSTION PLANT

Номер: US20220298602A1
Принадлежит: KAWASAKI JUKOGYO KABUSHIKI KAISHA

A combustion ash handling method of handling combustion ash discharged from a combustion furnace that combusts a petroleum-based fuel includes: separating the combustion ash into a heavy component and a light component by a dry-type separation technique; feeding the light component to the combustion furnace as a fuel; and recovering the heavy component. A metal such as vanadium is separated and extracted from the heavy component of the combustion ash. 1. A combustion ash handling method of handling combustion ash discharged from a combustion furnace that combusts a petroleum-based fuel , the combustion ash handling method comprising:separating the combustion ash into a heavy component and a light component by a dry-type separation technique;feeding the light component to the combustion furnace as a fuel; andrecovering the heavy component.2. The combustion ash handling method according to claim 1 , whereinseparating the combustion ash includes separating the combustion ash into the heavy component and the light component by dry-type specific gravity separation.3. The combustion ash handling method according to claim 1 , whereinseparating the combustion ash includes separating the combustion ash into the heavy component and the light component by sink float separation with use of a fluidized bed.4. The combustion ash handling method according to claim 3 , whereina fluidized medium of the fluidized bed is the combustion ash.5. The combustion ash handling method according to claim 1 , further comprising separating and extracting a metal from the heavy component that has been recovered claim 1 , the metal containing at least vanadium.6. A combustion ash handling system for handling combustion ash discharged from a combustion furnace that combusts a petroleum-based fuel claim 1 , the combustion ash handling system comprising:a dry-type separator that separates the combustion ash into a heavy component and a light component;a light component transfer line that feeds the ...

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21-05-2020 дата публикации

UV-PROTECTIVE COMPOSITIONS AND THEIR USE

Номер: US20200155428A1
Принадлежит:

Disclosed are compositions comprising inorganic UV-absorbing agents and the use of such compositions, in particular for protecting a subject or the surface of an inanimate object against a harmful effect of ultraviolet radiation. 1. A UV-protective composition which comprises particles of at least one inorganic UV-absorbing agent selected from the group consisting of (i) barium titanate (BaTiO) and (ii) bismuth vanadate (BiVO) , and which optionally comprises particles of an additional inorganic UV-absorbing agent selected from the group consisting of (iii) bismuth oxide (Bi2O) and (iv) doped zinc oxide (ZnO).2. The UV-protective composition according to claim 1 , wherein said at least one inorganic UV-absorbing agent is present in the composition as nanoparticles having at least one dimension of up to about 100 nm and said additional inorganic UV-absorbing agent claim 1 , if included claim 1 , is present in the composition as nanoparticles having at least one dimension of up to about 100 nm.3. The UV-protective composition according to or claim 1 , wherein at least 50% claim 1 , at least 90% claim 1 , at least 95% claim 1 , at least 97.5% or at least 99% of the number or of the volume of nanoparticles of the inorganic UV-absorbing agent(s) and/or of the additional inorganic UV-absorbing agent(s) claim 1 , if included claim 1 , present in the composition have each independently at least one dimension of up to about 100 nm.4. The UV-protective composition of claim 3 , wherein at least 90% of the number or the volume of nanoparticles of the inorganic UV-absorbing agent(s) and/or of the additional inorganic UV-absorbing agent(s) claim 3 , if included claim 3 , present in the composition have each independently at least one dimension of up to about 100 nm.5. The UV-protective composition of claim 4 , wherein at least 95% of the number or the volume of nanoparticles of the inorganic UV-absorbing agent(s) and/or of the additional inorganic UV-absorbing agent(s) claim 4 , ...

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15-06-2017 дата публикации

HEAT STORING SYSTEM

Номер: US20170167803A1
Принадлежит:

A heat storing system includes: a heat source that emits heat to a first thermal medium; and a heat storing unit. The heat storing unit includes a heat storing body container housing a heat storing body, and a thermal medium container housing a liquid phase thermal medium. The heat storing body stores or emits heat in accordance with phase change of the heat storing body. The heat storing unit is configured to conduct a cold heat emission mode in which the liquid phase thermal medium and a cooling medium exchange heat in the thermal medium container to evaporate the thermal medium such that cold heat is emitted to the cooling medium. 1. A heat storing system comprising:a heat source that generates heat and emits the heat to a first thermal medium; anda heat storing unit including a heat storing body storing heat, wherein: a heat storing body container housing the heat storing body, and', 'a thermal medium container housing a liquid-state second thermal medium that is evaporated by removing heat of a third thermal medium flowing outside the thermal medium container,, 'the heat storing unit includes'}the heat storing body container is configured to receive vapor of the second thermal medium generated in the thermal medium container,the heat storing body has a pore receiving the vapor of the second thermal medium,the heat storing body is configured to change to a solid-state first phase when the heat storing body has a temperature not more than a phase transition temperature and change to a solid-state second phase when the heat storing body has a temperature exceeding the phase transition temperature,the heat storing body is configured to store or emit heat in accordance with phase change between the first phase and the second phase, andthe heat storing unit is configured to be switchable betweena heat storing mode to store heat of the first thermal medium in the heat storing body by heat exchange between the first thermal medium and the heat storing body in the heat ...

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21-05-2020 дата публикации

Metallurgical And Chemical Processes For Recovering Vanadium And Iron Values From Vanadiferous Titanomagnetite And Vanadiferous Feedstocks

Номер: US20200157696A1
Автор: CARDARELLI François
Принадлежит:

The present disclosure broadly relates to a process for recovering vanadium, iron, titanium and silica values from vanadiferous feedstocks. More specifically, but not exclusively, the present disclosure relates to a metallurgical process in which vanadium, iron, titanium and silica values are recovered from vanadiferous feedstocks such as vanadiferous titanomagnetite, iron ores, vanadium slags and industrial wastes and by-products containing vanadium. The process broadly comprises digesting the vanadiferous feedstocks into sulfuric acid thereby producing a sulfation cake; dissolving the sulfation cake and separating insoluble solids thereby producing a pregnant solution; reducing the pregnant solution thereby producing a reduced pregnant solution; and crystallizing ferrous sulfate hydrates from the reduced pregnant solution, producing an iron depleted reduced solution. The process further comprises removing titanium compounds from the iron depleted reduced solution thereby producing a vanadium-rich pregnant solution; concentrating vanadium and recovering vanadium products and/or a vanadium electrolyte. 1. A process for recovering vanadium , iron , titanium and silica values from vanadiferous feedstocks , the process comprising:digesting the vanadiferous feedstocks into sulfuric acid thereby producing a sulfation cake;dissolving the sulfation cake and separating insoluble solids thereby producing a pregnant solution;reducing the pregnant solution thereby producing a reduced pregnant solution;crystallizing ferrous sulfate hydrates from the reduced pregnant solution, producing an iron depleted reduced solution; andremoving titanium compounds from the iron depleted reduced solution thereby producing a vanadium-rich pregnant solution.2. The process of claim 1 , further comprising treating the vanadium-rich pregnant solution to recover vanadium products and/or a vanadium electrolyte.3. The process of or claim 1 , wherein the vanadiferous feedstocks comprise materials ...

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25-06-2015 дата публикации

Bi-Functional Catalysts for Oxygen Reduction and Oxygen Evolution

Номер: US20150180046A1
Принадлежит: STC.UNM

A porous metal-oxide composite particle suitable for use as a oxygen reduction reaction or oxygen evolution reaction catalyst and sacrificial support based methods for making the same. 1. A method for forming a porous metal oxide material comprising:providing sacrificial template particles;reacting one or more metal precursors and an oxide precursor onto the sacrificial template particles to produce coated template particles;heat treating the coated template particles; andremoving the sacrificial template particles to produce a highly dispersed, self-supported, high surface area electrocatalytic material.2. The method of wherein the metal is a transition metal.3. The method of wherein at least one of the metal precursors is a metal citrate or metal nitrate.4. The method of wherein the step of reacting one or more metal precursors and an oxide precursor onto the sacrificial template particles comprises mixing a colloidal suspension of template particles with a solution containing a transition metal citrate or nitrate and sodium nitrate.5. The method of wherein the step of heat treating the coated template particles comprises calcination.6. The method of wherein the step of reacting one or more metal precursors and an oxide precursor onto the sacrificial template particles comprises mixing a colloidal suspension of template particles claim 1 , sucrose and urea with a solution containing transition metal precursors.7. The method of wherein the step of heat treating the coated template particles comprises pyrolyzation claim 1 , followed by calcination.8. The method of wherein the step of removing the sacrificial template particles comprises chemical etching.9. The method of wherein the chemical etchant is HF.10. The method of wherein the metal precursor is selected from the group consisting of cobalt nitrate claim 1 , zirconium oxynitrate hydrate claim 1 , indium chloride tetrahydrate claim 1 , venadyl sulfate hydrate claim 1 , praseodymium nitrate hexahydrate claim 1 , ...

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22-06-2017 дата публикации

COMPOSITE NANOMATERIALS AND MICROMATERIALS, FILMS OF SAME, AND METHODS OF MAKING AND USES OF SAME

Номер: US20170174526A1
Принадлежит:

Composite nano- and micromaterials and methods of making and using same. The composite materials comprise crystalline materials (e.g., binary and ternary vanadium oxides) in an amorphous or crystalline material (e.g., oxide, sulfide, and selenide materials). The materials can be made using sol-gel processes. The composite materials can be present as a film on a substrate. The films can be formed using preformed composite materials or the composite material can be formed in situ in the film forming process. For example, films of the materials can be used in fenestration units, such as insulating glass units deployed within windows. 1. A composition comprising a crystalline vanadium oxide nanomaterial and/or micromaterial encapsulated in an amorphous or crystalline oxide , sulfide , or selenide matrix.2. The composition of claim 1 , wherein the vanadium oxide nanomaterial and/or micromaterial is in the form of nanoparticles claim 1 , microparticle claim 1 , nanowires claim 1 , microwires claim 1 , nanorods claim 1 , microrods claim 1 , nanospheres claim 1 , microspheres claim 1 , nanostars claim 1 , microstars claim 1 , or a combination thereof.3. The composition of claim 1 , wherein the amorphous oxide matrix comprises silicon oxide claim 1 , titanium oxide claim 1 , vanadium oxide claim 1 , zinc oxide claim 1 , hafnium oxide claim 1 , cerium oxide claim 1 , molybdenum oxide claim 1 , or a combination thereof.4. The composition of claim 1 , wherein the vanadium oxide nanomaterial and/or vanadium oxide micromaterial is doped.5. A substrate comprising a film of the composition of disposed on at least a portion of a surface of the substrate.6. The substrate of claim 5 , wherein the substrate is glass claim 5 , silicon oxide claim 5 , sapphire claim 5 , alumina claim 5 , polymer claim 5 , plastic claim 5 , or indium tin oxide-coated glass.7. The substrate of claim 5 , wherein the film of the composition of disposed on the at least a portion of a surface of the substrate ...

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23-06-2016 дата публикации

TRANSPARENT CONDUCTING FILMS INCLUDING COMPLEX OXIDES

Номер: US20160180982A1
Принадлежит:

Transparent conducting films including an alkaline earth, transition metal oxide and their optimization of electrical conductivity and optical transparency by aliovalent substitution, which are useful as electrodes for semiconductors and other electronic devices are disclosed. Such materials include thin films of an aliovalent substituted transition metal oxides of Formula (I): AA′BB′O(I) or a transition metal oxide of Formula (II): (ABO)m(A′B′O)n. 1. A transparent conducting film comprising a transition metal oxide of formula:{'br': None, 'sub': 1-x', 'x', '1-y', 'y', '3-d, 'AA′′BB′O\u2003\u2003(I)'}wherein A and A′ are different from each other and A represents one or more divalent alkaline earth cations; A′ represents either one or more trivalent cations or one or more monovalent cations; B and B′ are different from each other and B represents a transition metal selected from group VB; and B′ represents a transition metal from the groups VB, IVB, VIB, IVA and/or group IIIA; d is a value between −0.5≦d≦0.5; and the values for x and y are 0≦x≦1, 0≦y≦1; provided that when y is 0, B is not vanadium.3. The film according to claim 1 , wherein A′ is present and represents one or more of a trivalent cation of lanthanum claim 1 , cerium claim 1 , praseodymium claim 1 , neodymium claim 1 , promethium claim 1 , samarium claim 1 , europium claim 1 , gadolinium claim 1 , terbium claim 1 , dysprosium claim 1 , holmium claim 1 , erbium claim 1 , thulium claim 1 , ytterbium claim 1 , or lutetium to adjust a Fermi level position in a conduction band of the transition metal oxide.4. The film according to claim 1 , wherein A′ is present and represents one or more of a monovalent ion of lithium claim 1 , sodium claim 1 , potassium claim 1 , rubidium or cesium to adjust a Fermi level position in a conduction band of the transition metal oxide.5. The film according to claim 1 , wherein B′ is present and represents one or more group VIB transition metal elements to adjust a Fermi level ...

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21-06-2018 дата публикации

NANOFIBERS ELECTRODE AND SUPERCAPACITORS

Номер: US20180174767A1
Автор: Kumar Vipin, LEE Pooi See
Принадлежит:

According to the present disclosure, a method for synthesizing a free-standing flexible electrode is provided. The method includes the steps of mixing a solution comprising vanadium powder, molybdenum powder and hydrogen peroxide to form a mixture comprising nanofibers represented by the formula of VMoOnHO, filtering the mixture to form an electrode comprising the nanofibers, treating the electrode with an acidic solution, contacting the acid-treated electrode with a solution comprising monomers of a conductive polymer, and polymerizing the monomers in a medium comprising an oxidizing agent to form the conductive polymer. According to the present disclosure, there is also a free-standing flexible electrode comprising nanofibers comprised of molybdenum, vanadium and a conductive polymer, wherein the electrode is represented by a formula of X—V MoOn-HO. In this formula, X is the conductive polymer and n is independently 1 or 2. According to the present disclosure, storage devices comprising the electrode as defined above, are also provided. 2. The method of claim 1 , wherein the molybdenum powder comprises about 85 to about 95 wt % of the mixed vanadium and molybdenum powders.3. The method of claim 1 , wherein the vanadium powder comprises about 5 to about 15 wt % of the mixed vanadium and molybdenum powders.4. (canceled)5. The method of claim 1 , wherein the hydrogen peroxide comprises a concentration of about 10 to about 25 wt %.6. (canceled)7. The method of claim 1 , further comprising heating the mixture to about 170 to about 190° C. to form the nanofibers.8. (canceled)9. The method of claim 1 , wherein the mixture is filtered under vacuum and/or via a flow directed assembly.10. (canceled)11. The method of claim 1 , wherein the filtered electrode is treated with the acidic solution for about 5 to about 10 hours.1213-. (canceled)14. The method of claim 1 , further comprising drying the acid-treated electrode before contacting the acid-treated electrode with the ...

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21-06-2018 дата публикации

Graphene-Vanadium Oxide Nanowire, Method for Preparation Thereof, Positive Active Material Comprising the Same and Lithium Battery Comprising the Positive Active Material

Номер: US20180175385A1
Принадлежит:

The present disclosure is directed to a graphene-vanadium oxide nanowire including a nanowire core including vanadium oxide and a shell formed on the surface of the nanowire core and including graphene oxide. The graphene-vanadium oxide nanowire having improved capacity stability can be provided by using the graphene-vanadium oxide nanowire according to the present disclosure, the method for preparing the same, and a positive active material and a secondary battery including the same. In addition, by using the graphene-vanadium oxide nanowire according to the present disclosure as a positive active material, it is possible to provide a secondary battery having improved cycle characteristics and capacity retention rates. 1. A graphene-vanadium oxide nanowire comprising a nanowire core including vanadium oxide and a shell formed on a surface of the nanowire core and including graphene oxide.2. The graphene-vanadium oxide nanowire according to claim 1 , wherein the shell has graphene and graphene oxide.3. The graphene-vanadium oxide nanowire according to claim 1 , wherein the vanadium oxide includes at least one selected from a group consisting of VO claim 1 , VO claim 1 , and VO.4. The graphene-vanadium oxide nanowire according to claim 1 , wherein the nanowire core and the shell are in a mass ratio of 1:1 to 10:1.5. An active material for a secondary battery claim 1 , the active material comprising a nanowire core including vanadium oxide claim 1 , and a shell formed on a surface of the nanowire core and including graphene oxide.6. The active material for a secondary battery according to claim 5 , wherein the shell has graphene and graphene oxide.7. The active material for a secondary battery according to claim 5 , wherein the vanadium oxide includes at least one selected from a group consisting of VO claim 5 , VO claim 5 , and VO.8. The active material for a secondary battery according to claim 5 , wherein the nanowire core and the shell are in a mass ratio of 1:1 ...

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08-07-2021 дата публикации

ANISOTROPIC MATERIALS AND METHODS OF FORMING ANISOTROPIC MATERIALS EXHIBITING HIGH OPTICAL ANISOTROPY

Номер: US20210206652A1
Принадлежит:

A method for forming a crystalline material having an anisotropic, quasi-one-dimensional crystal structure is disclosed. In various embodiments, the method includes: mixing a plurality of precursor materials together to form a combined precursor material, the plurality of precursor materials including a transition-metal ion or a main group ion and at least one of an alkaline earth ion or an alkali metal ion; and reacting the combined precursor material to obtain the crystalline material, the crystalline material having a formula ABX3, wherein A is the at least one of the alkaline earth ion or the alkali metal ion and B is the transition-metal ion surrounded by six anions (X), and wherein the quasi-one-dimensional anisotropic crystal provides a birefringence of at least 0.03, defined as the absolute difference in the real part of the complex-refractive-index values along different crystal axes, in at least a portion of one or N both of the visible-wave spectrum or the infrared spectrum. 1. A method for forming a crystalline material having an anisotropic , quasi-one-dimensional crystal structure , comprising:mixing a plurality of precursor materials together to form a combined precursor material, the plurality of precursor materials including a transition-metal ion or a main group ion and at least one of an alkaline earth ion or an alkali metal ion; and{'sub': '3', 'reacting the combined precursor material to obtain the crystalline material, the crystalline material having a formula ABX, wherein A is the at least one of the alkaline earth ion or the alkali metal ion and B is the transition-metal ion surrounded by six anions (X), and wherein the quasi-one-dimensional anisotropic crystal provides birefringence of at least 0.03, defined as the absolute difference in the real part of the complex refractive-index values along different crystal axes, in at least a portion of one or both of the visible-wave spectrum or the infrared-wave spectrum.'}2. The method of claim 1 , ...

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30-06-2016 дата публикации

Composite postiive electrode active material, method of manufacturing the same, positive electrode including the composite positive electrode active material, and lithium secondary battery including the positive electrode

Номер: US20160190575A1

A composite positive electrode active material including: an overlithiated layered oxide (OLO) including vanadium (V) and magnesium (Mg), wherein the vanadium and magnesium have a molar ratio of about 1:2. Also a method of manufacturing the composite positive electrode active material, a positive electrode including the composite positive electrode, and a lithium battery including the positive electrode.

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28-06-2018 дата публикации

Nanoscale pore structure cathode for high power applications and material synthesis methods

Номер: US20180183089A1
Принадлежит: A123 Systems LLC

A lithium iron phosphate electrochemically active material for use in an electrode and methods and systems related thereto are disclosed. In one example, a lithium iron phosphate electrochemically active material for use in an electrode is provided including, a dopant comprising vanadium and optionally a co-dopant comprising cobalt.

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