Alkylation process
Реферат: 559,053. Alkylation process. SHELL DEVELOPMENT CO. May 27, 1942, No. 7180. Convention date, Oct. 11, 1941. [Class 2 (iii)] Alkylatable organic compounds such as isoparaffins, cyclopentanes, cyclohexanes, aromatic hydrocarbons, phenols, cresols, aniline, nitrobenzene, and halobenzenes, are alkylated with a normally liquid olefine capable of forming an active oxygen-containing compound which tends to shorten the life of the alkylation catalyst, the alkylation taking place in the substantial absence of said active oxygencontaining compound. Its absence may be obtained by adding an antioxidant such as a naphthol, tertiary butyl phenol or cresol, or resorcinol, to the olefine, or distilling the olefine to obtain a fraction having a lower concentration of said oxygen-containing compound, or by treating the olefine with reducing agents such as sodium bisulphite or by using an oxalic acid-sulphuric acid mixture. The olefine used is preferably a polymer of a lower boiling olefine, such as ethylene, propylene, butylenes, isobutylene, amylenes, cyclopentene, cyclohexene, and methyl cyclohexene, or the polymers may be made from the corresponding alcohols. Interpolymers of isobutylene and secondary butylenes may be used. The catalyst may be sulphuric, chlorosulphonic, fluorosulphonic, hydrofluoric or hydrofluoroboric acid, or Friedel-Crafts type catalysts such as aluminium chloride, aluminium chloridekerosene, aluminium chloride-sodium chloride or aluminium chloride with antimony trichloride. Specifications 479,657, 514,043, 527,720 and 553,749 are referred to.
Sulfuric acid catalyzed alkylation process
Номер патента: US4209656A. Автор: Gerald F. Prescott,Charles T. Lewis, Jr.. Владелец: Texaco Inc. Дата публикации: 1980-06-24.