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临氢条件下NiMoS/γ-Al2O3催化辛烯-1与H2S的反应
引用本文:吕岩,周文博,夏道宏,周玉路,项玉芝,薛晓红.临氢条件下NiMoS/γ-Al2O3催化辛烯-1与H2S的反应[J].石油学报(石油加工),2012,28(5):744-749.
作者姓名:吕岩  周文博  夏道宏  周玉路  项玉芝  薛晓红
作者单位:1. 中国石油大学 重质油国家重点实验室 化学工程学院,山东 青岛 266580;
2. 中国石油天然气管道局天津设计院,天津 300457
基金项目:国家自然科学基金(21076231)和山东省自然科学基金项目(2009ZRA05107)资助
摘    要: 在高压反应釜中临氢条件下研究了NiMoS/γ-Al2O3催化辛烯-1与H2S的反应,考察了反应温度、H2S含量和烯烃体积分数对反应产物的影响,对反应产物进行GC-MS分析,探讨了辛烯-1与H2S的反应机理。结果表明,辛烯-1与H2S反应主要生成硫醇类和硫醚类化合物,辛烯-1本身还会发生加氢饱和反应和双键迁移异构化反应。随着反应温度升高,反应产物中的硫醇硫和总硫的量均逐渐减少,同时促进了辛烯-1的加氢饱和反应。反应体系中H2S的含量越高,产物中硫醇硫和硫醚硫的含量越大;而且H2S还会促进辛烯-1的双键迁移异构化反应,抑制辛烯-1的加氢饱和反应。随着反应体系中辛烯-1体积分数增大,产物中总硫的含量不断增大,而硫醇硫的含量先增大后减小,此外,辛烯-1的异构化产物和加氢饱和产物也会随之不断增多。

关 键 词:辛烯-1  硫化氢  硫醇  硫化物  反应机理

Reaction Between Octene-1 and H2S Over NiMoS/γ-Al2O3 catalyst under Presence of H2
LV Yan,ZHOU Wenbo,XIA Daohong,ZHOU Yulu,XIANG Yuzhi,XUE Xiaohong.Reaction Between Octene-1 and H2S Over NiMoS/γ-Al2O3 catalyst under Presence of H2[J].Acta Petrolei Sinica (Petroleum Processing Section),2012,28(5):744-749.
Authors:LV Yan  ZHOU Wenbo  XIA Daohong  ZHOU Yulu  XIANG Yuzhi  XUE Xiaohong
Affiliation:1. State Key Laboratory of Heavy Oil Processing, College of Chemical Engineering, China University of Petroleum, Qingdao 266580, China; 2. China Petroleum Pipeline Bureau Tianjin Design Institute, Tianjin 300457, China
Abstract:The reaction between octene-1 and H2S was studied over NiMoS/γ-Al2O3 catalyst in the high pressure autoclave. The effects of reaction temperature, H2S  content and volume fraction of octene1 on the reaction between octene-1 and H2S  under the presence of H2 were investigated. The composition of the product was analyzed by GC-MS, and the reaction mechanism was discussed. The results showed that the sulfur compounds including mercaptans and thioethers were formed in the reaction between octene-1 and H2S , and that hydrogenation and double bond isomerization reactions of octene-1 occurred. The contents of mercaptan sulfides and total sulfides in the product both increased with the reaction temperature rising, meanwhile the hydrogenation reaction of octene-1 could be promoted. The contents of mercaptan sulfides and thioether sulfides in the reaction system increased with the H2S  content increasing; in addition, the isomerization of reaction of octene-1 could be promoted and the hydrogenation of octene-1 was inhibited. As the octene-1 volume fraction increased, the contents of total sulfides increased while the contents of mercaptan sulfides first increased and then decreased, moreover, the products of isomerization and hydrogenation reaction of octene-1 both increased.
Keywords:octene-1  hydrogen sulfide  mercaptan  sulfide  reaction mechanism
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