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Shape selective alkylation of biphenyl with propene on SAPO-11 catalysts

โœ Scribed by T. Matsuda; T. Kimura; E. Herawati; C. Kobayashi; E. Kikuchi


Publisher
Elsevier Science
Year
1996
Tongue
English
Weight
526 KB
Volume
136
Category
Article
ISSN
0926-860X

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๐Ÿ“œ SIMILAR VOLUMES


Alkylation of biphenyl with propene on H
โœ Takeshi Matsuda; Tatsuo Urata; Eiichi Kikuchi ๐Ÿ“‚ Article ๐Ÿ“… 1995 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 578 KB

Alkylation of biphenyl with propene to produce 4,4'-diisopropylbiphenyl (4,4'-DIPB) was investigated using silica-alumina and zeolites such as faujasite Y, beta, offretite, mordenite, ZSM-8, and ZSM-5 as catalysts. Of these, mordenite was the most active and selective to 4,4'-DIPB. The highest yield

Shape-selective alkylation of naphthalen
โœ Chunshan Song; Stephen Kirby ๐Ÿ“‚ Article ๐Ÿ“… 1994 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 791 KB

Naphthalene alkylation with isopropanol was studied at 250ยฐC using several proton-form mordenites (HM) and Y-zeolites. HM catalysts afforded 2-isopropylnaphthalene (ZIPN) as the dominant product, whereas the Y-zeolites (HY and LaHY) gave l-IPN as a major product. HM displayed better selectivity to 2