2014
DOI: 10.1016/j.cattod.2013.10.015
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Selective synthesis of linear alkylbenzene by alkylation of benzene with 1-dodecene over desilicated zeolites

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Cited by 38 publications
(27 citation statements)
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“…Compared with the HZ5 catalyst, the number of Lewis acid sites increases after treatment of the catalysts with LiOH, NaOH, KOH, and CsOH, respectively (Table 2). It should be noted that Lewis acid sites are generated due to the formation of extraframework Al species, which is consistent with previous reports [49]. Notably, the ATHZ5-Na catalyst contains the highest amount of Brönsted acid sites, which can be attributed to the proper alkali treatment leading to higher Al content (i.e., a lower Si/Al ratio) [50].…”
Section: Pyridine Ft-ir Analysissupporting
confidence: 78%
“…Compared with the HZ5 catalyst, the number of Lewis acid sites increases after treatment of the catalysts with LiOH, NaOH, KOH, and CsOH, respectively (Table 2). It should be noted that Lewis acid sites are generated due to the formation of extraframework Al species, which is consistent with previous reports [49]. Notably, the ATHZ5-Na catalyst contains the highest amount of Brönsted acid sites, which can be attributed to the proper alkali treatment leading to higher Al content (i.e., a lower Si/Al ratio) [50].…”
Section: Pyridine Ft-ir Analysissupporting
confidence: 78%
“…Lewis acids may be involved as catalysts for the conversion, in particular, of more basic molecules, such as "normal" n-bases [15], as well as of aromatics [16,17], which are Page 3 of 29 A c c e p t e d M a n u s c r i p t 3 stronger -bases than olefins. Lewis acidity of protonic zeolites in fact gives rise to an additional or different functionality for catalysis with respect to Brønsted acidity [18,19].…”
mentioning
confidence: 99%
“…The authors performed the alkylation reaction using the benzene:1-alkene molecular ratio of 10:1 at temperatures ranging from 80°C to 160°C. It was shown that the composite material was less active than the dealuminated or desilicated mordenites [19,12]. The conversion of 1-dodecene was only 48% at the temperature of 120°C in the 120 min of reaction time.…”
Section: Introductionmentioning
confidence: 96%
“…These types of Friedel-Crafts catalysts are highly toxic, create a substantial amount of waste, and cause severe corrosion problems [6]. Based on the latter, a great effort is expended to replace these F-C catalysts by solid acid catalysts such as zeolites; for example, zeolite Y [7][8][9], beta zeolite [10,11], mordenites [12,13], heteropolyacids [14], clays [15] and ionic liquids [16] have been widely investigated for this reaction.…”
Section: Introductionmentioning
confidence: 99%