NiY分子筛表面酸性影响其选择性吸附脱硫性能的机理研究  

Mechanism of effects of surface acidity on performance of adsorption desulfurization of NiY zeolites

作　　者：宋丽娟[1] 胡月婷[1] 秦玉才[1] 于文广[2] 张晓彤[1] 

机构地区：[1]辽宁石油化工大学辽宁省石油化工催化科学与技术重点实验室,辽宁抚顺113001 [2]中国科学院大连化学物理研究所,辽宁大连116023

出　　处：《燃料化学学报》2016年第9期1082-1088,共7页Journal of Fuel Chemistry and Technology

基　　金：国家自然科学基金(21076100;21376114);中国石油天然气股份有限公司炼油催化剂重大专项(10-01A-01-01-01)资助~~

摘　　要：采用原位红外光谱技术,以噻吩、环己烯和苯为模型探针分子,分别考察单一烃分子在NiY分子筛上的吸附与反应行为以及噻吩与烯烃、芳烃间的竞争吸附和催化反应行为。单一探针分子吸附研究发现,NiY分子筛中与Ni物种相关的Lewis(L)酸位是噻吩的选择性吸附活性位;噻吩和环己烯在NiY分子筛中Brnsted(B)酸位上发生的质子化和低聚反应明显弱于HY分子筛。双探针分子竞争吸附研究发现,环己烯二聚体在NiY中强B酸位上的强化学吸附与噻吩存在显著的竞争吸附行为。另外,苯和噻吩在NiY上的竞争吸附现象在373K时明显减弱。由此,在选择性吸附脱硫过程中,减少吸附剂表面B酸中心可降低烯烃对噻吩的竞争吸附,另外适当提高吸附体系的温度可以有效避免芳烃对噻吩的竞争吸附。The adsorption behaviors of thiophene, cyclohexene and benzene, and competitive adsorption of thiophene ＆ cyclohexene, and thiophene ＆ benzene over NiY zeolites were studied by in situ Py-FTIR spectroscopy method. The results of single probe molecular adsorption indicate that the Lewis （ L ） acid sites according to Ni species are the major active centers for the thiophene adsorption, more over the Br-nsted （ B） acid sites of the NiY and HY are the catalytic active centers of the protonation and oligomerization of thiophene and cyclohexene, while the reaction intensity on NiY is significantly weaker than that on HY zeolite. The competitive adsorption results show that the strongly adsorbed dimeric cyclohexene on B acidic sites in NiY zeolite plays a significant competitive adsorption to thiophene adsorption behavior. The effective solutions to solve the competitive adsorption from olefins and aromatics to thiophene are to reduce the surface B acid centers of the adsorbent and to increase temperature of adsorption system.

关 键 词：原位红外光谱 NiY分子筛 表面酸性 吸附脱硫 竞争吸附 

分 类 号：O643[理学—物理化学]