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NiY分子筛选择性吸附脱硫性能及作用机理

宋丽娟 潘明雪 秦玉才 鞠秀芳 段林海 陈晓陆

高等学校化学学报2011,Vol.32Issue(3):787-792,6.
高等学校化学学报2011,Vol.32Issue(3):787-792,6.

NiY分子筛选择性吸附脱硫性能及作用机理

Selective Adsorption Desulfurization Performance and Adsorptive Mechanisms of NiY Zeolites

宋丽娟 1潘明雪 1秦玉才 1鞠秀芳 1段林海 1陈晓陆1

作者信息

  • 1. 辽宁石油化工大学辽宁省石油化工重点实验室,抚顺,113001
  • 折叠

摘要

Abstract

NiY zeolites were prepared by liquid phase ion exchange method and the adsorbents were characterized by XRD, TEM, ICP, nitrogen adsorption and Py-IR. The adsorptive behavior of thiophene (T),2-methylthiophene ( 2-MT), 3-methylthiophene ( 3-MT ), tetrahydrothiophene ( THT ), benzothiophene ( BT ),dibenzothiophene( DBT), 4-methyldibenzothiophene (4-MDBT) and 4,6-dimethyldiben-zothiophene (4,6-DMDBT) on NiY zeolites were investigated by a fixed bed, gas chromatography-suffur chemiluminescence detector(GC-SCD) and Fourier transform infrared(FTIR). The results show that the breakthrough adsorption capacities of different suffur compounds are in the order of THT > BT ≈ DBT ≈ 4,6-DMDBT > 4-MDBT >3-MT≈2-MT > T, indicating that the steric hindrance of sulfur compounds is not the crucial factor for their adsorptive properties on NiY zeolites. The mechanisms of thiophene and thiophene derivatives interacting with NiY zeolites are different, but the direct S-M interaction is the domain process. Thiophene and thiophene alkyl complex adsorbed on the surface acidic sites of the sorbents can subsequently undergo the opening of the heterocyclic rings and then to form some larger suffur compounds. These polymer molecules will plug the pore of zeolite, resulting in the decreasing of the desulfurization capacity of the NiY. Adsorption mechanisms and surface acidity of NiY zeolites are the key factors for the selective adsorption desuffurization.

关键词

液相离子交换/NiY分子筛/吸附脱硫/表面酸性

Key words

Liquid phase ion exchanging/ NiY zeolite/ Adsorptive desulfurization/ Surface acidity

分类

化学化工

引用本文复制引用

宋丽娟,潘明雪,秦玉才,鞠秀芳,段林海,陈晓陆..NiY分子筛选择性吸附脱硫性能及作用机理[J].高等学校化学学报,2011,32(3):787-792,6.

基金项目

国家"九七三"计划项目(批准号:2007CB216403)和国家自然科学基金(批准号:20976077,21076100)资助. (批准号:2007CB216403)

高等学校化学学报

OA北大核心CSCDCSTPCD

0251-0790

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