2008
DOI: 10.1016/j.cattod.2007.08.017
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Gasoline desulfurization by catalytic alkylation over silica-supported heteropolyacids: From model reaction to real feed conversion

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Cited by 50 publications
(23 citation statements)
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“…1. Although the reaction of alkylation have reported at lower temperature that could be taken place, it could not act effective on high sulfuric content gasoline [13]. While the temperature below 140°C, the conversion of thiophene is no more than 57.5%.…”
Section: The Effect Of Reaction Temperature On Conversion Of Thiophenementioning
confidence: 98%
See 1 more Smart Citation
“…1. Although the reaction of alkylation have reported at lower temperature that could be taken place, it could not act effective on high sulfuric content gasoline [13]. While the temperature below 140°C, the conversion of thiophene is no more than 57.5%.…”
Section: The Effect Of Reaction Temperature On Conversion Of Thiophenementioning
confidence: 98%
“…Several works had been investigated about the OATS zeolites catalysts, such as the Hb, MCM-41, MCM-22 [11][12][13]. However, the activity of the acid catalyst and the alkylation conditions are hardly to be chosen which will lead to the other competitive reactions, the aromatics alkylation, since they could decrease the selectivity of the OATS and increase the losses in gasoline yield.…”
Section: Introductionmentioning
confidence: 99%
“…However, the increment of conversion was limited. It showed that mono-olefins also reacted with thiophene [9,12], which led to an improvement of conversion of thiophene. Due to the higher reaction activity of diene than mono-olefins [8], the conversion of thiophene only had a slight increase when the olefin was introduced to the system.…”
Section: Alkylation Performance Of Different Kind Of Thiophenic Sulfurmentioning
confidence: 99%
“…Many acidic catalysts are proposed, with either Brunsted or Lewis acidity, including various zeolites (b-zeolite, MCM-22, MCM-41, USY,…), phosphoric acid on kieselguhr, H 3 PW 12 O 40 /Fe 2 O 3 , etc. [7,[9][10][11][12]. However, the acid catalyst causes easily the other competitive reactions under the alkylation conditions, such as the aromatics alkylation, polymerization of olefins or diene, over-alkylation of thiophene and so on.…”
Section: Introductionmentioning
confidence: 99%
“…This process is used to convert thiophene, benzenethiophene, dibenzothiophene and 4,6-dimethyldibenzothiophene into sulfones and sulfoxides in presence of oxidizing agent and sulfones and sulfoxides are easily separated by extraction with polar solvent [16][17][18][19]. The ODS process widely studied in various systems, such as organic acid [20], heteropolyoxo-metalates [21], ionic liquid [22,23], molecular sieve [24,25] and photocatalysts [26], heteropoly acid (HPA) catalysts [27][28][29], HPA catalysts, especially those having the keggin structure, have been determined to be very effective for the oxidation of sulfur containing compounds in a liquid-liquid two phase system. Li et al [30] reported mesoporous silica pillared clay incorporated with phosphotungstic acid.…”
Section: Introductionmentioning
confidence: 99%