| 离子液体催化剂用于煤焦化苯深度脱硫制无硫苯 |
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| 引用本文： | 周霞萍,王琰靓,孟繁伟,樊兴明,秦松波. 离子液体催化剂用于煤焦化苯深度脱硫制无硫苯[J]. 中国化学, 2008, 26(4): 607-610. DOI: 10.1002/cjoc.200890114 |
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| 作者姓名： | 周霞萍 王琰靓 孟繁伟 樊兴明 秦松波 |
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| 作者单位： | 华东理工大学能源化工系,上海 200237 |
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| 摘 要： | 从扩大有机合成用苯的需求出发,采用研制的离子液体催化剂考察了煤焦化苯深度脱硫制无硫苯的过程。结果表明：N-甲基咪唑硫酸氢盐[Hmim][HSO4]离子液体催化剂脱噻吩效果与其酸函数值有关。本文采用Hammett指示剂测定离子液体的酸函数H0,并得出：在-4至-12的范围,离子液体催化剂可以使煤焦化苯噻吩脱至0. 5mg/L以下。与固体酸催化机理相似,酸量和酸强度一定的离子液体催化剂通过Friedel-Crafts反应形成烷基噻吩等,与苯的物性拉开距离,对苯的分离精制是必不可少的,但是过多、过强的[Hmim][HSO4]酸值也更有利于苯-噻吩-烯烃共聚合等副反应的发生,从而影响离子液体催化剂重复使用的寿命。本研究利用煤焦化苯脱硫反应形成的噻吩衍生物作为提供电荷流通的聚合物,将反复使用后性能不佳的离子液体成分等作为“受电子型”和“给电子型”的掺杂剂,进行导电（抗静电）材料的制备。结果显示：对煤焦化苯脱硫形成的噻吩衍生物等可以用于掺杂导电材料的试制。
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| 关 键 词： | 煤焦化苯 离子液体 酸性离子液体 脱噻吩 无硫苯 |
| 收稿时间： | 2007-11-01 |
| 修稿时间： | 2008-02-20 |
Ionic Liquid Catalyst Used in Deep Desulfuration of the Coking Benzene for Producing Sulfurless Benzene |
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| Xia‐Ping ZHOU,Yan‐Liang WANG,Fan‐Wei MENG,Xing‐Ming FAN,Song‐Bo QIN. Ionic Liquid Catalyst Used in Deep Desulfuration of the Coking Benzene for Producing Sulfurless Benzene[J]. Chinese Journal of Chemistry, 2008, 26(4): 607-610. DOI: 10.1002/cjoc.200890114 |
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| Authors: | Xia‐Ping ZHOU Yan‐Liang WANG Fan‐Wei MENG Xing‐Ming FAN Song‐Bo QIN |
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| Affiliation: | 1. Tel.: 027‐87543232;2. Fax: 086‐027‐87543632;3. Department of Chemical Engineering for Energy Resources Technology, East China University of Science & Technology, Shanghai 200237, China |
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| Abstract: | For the widening need of benzene used in organic synthesis, ionic liquid catalyst was prepared to study the process of deep desulfuration in the coking benzene. The result shows that the effect of de‐thiophene by the ionic liquid catalyst (N‐methyl imidazolium hydrogen sulfate [Hmim][HSO4]) is related to its acid function value. Hammett indicator was used to determine the acid function value H0 of the ionic liquid. It can be concluded that while the acid function value is in the range from ?4 to ?12, the ionic liquid catalyst can make the concentration of thiophene in the coking benzene be under 0.5 mg·L?1. Similarly to the catalytic mechanism of solid acid, with a certain acid quantity and strength, the ionic liquid catalyst helps to form alkyl thiophene through Friedel‐Crafts reaction, which differs from the character of benzene and it is absolutely necessary for the separation and refinement of benzene. But overabundant quantity and higher acid value of [Hmim][HSO4] are more suitable for the side copolymerization of benzene, thiophene and alkene, thereby affecting repeated use of the ionic liquid catalyst([Hmim][HSO4]). In our research, thiophene derivant produced by desulfurization in the coking benzene was used as the polymer to provide the passing channel of the charges. The ionic liquid composition in poor performance after repeated use was made to prepare conductive material (resisting to static electricity) as an "electron‐receiving" and "electron‐giving" doping agent. The result shows that thiophene derivant after desulfuration in the coking benzene can be used to prepare doping conductive materials. |
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| Keywords: | coking benzene ionic liquid acid ionic liquid de‐thiophene sulfurless benzene |
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