Gasoline alkylation desulfurization over Amberlyst 35 resin: Influence of methanol and apparent reaction kinetics

被引:33
|
作者
Guo, Benshuai [1 ]
Wang, Rong [1 ]
Li, Yonghong [1 ,2 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Key Lab Green Chem Technol, Tianjin 300072, Peoples R China
[2] Natl Engn Res Ctr Distillat Technol, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金;
关键词
Alkylation; Desulfurization; Amberlyst; 35; Thiophenic sulfurs; Kinetics; H-BETA-ZEOLITE; THIOPHENIC SULFUR; DEEP DESULFURIZATION; OLEFIN ALKYLATION; HYDRODESULFURIZATION; 3-METHYLTHIOPHENE; 2-METHYL-2-BUTENE; DIMERIZATION; PERFORMANCE;
D O I
10.1016/j.fuel.2010.10.010
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Gasoline desulfurization is receiving attention worldwide due to the increasing stringent regulations on sulfur content for environmental protection purpose. As conventional hydrotreating technology leads to significant octane number loss and processing costs, the gasoline alkylation desulfurization process, which consists of weighing down the sulfuric compounds by catalytic alkylation with olefins present in the feed and distillation followed by, is a rather attractive way. In this paper, firstly alkylation of thiophenic compounds was researched over macroporous sulfonic resin Amberlyst 35 in methanol presence to increase the selectivity of catalyst, then kinetics of thiophenic sulfurs alkylation in FCC gasoline was researched without and with methanol. Results found that appropriate methanol (<= 2 wt.% methanol in model gasoline and <= 1 wt.% methanol in FCC gasoline) could inhibit olefins oligomerization significantly without influence on the conversions of thiophenic compounds. The alkylation of thiophenic sulfurs could be described as pseudo first order reaction regardless of the existence of methanol. The introduction of methanol decreases the reaction rate constant and increases the activation energy of alkylation reactions. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:713 / 718
页数:6
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