介孔ZSM-5负载Ni催化剂的制备及乙烯齐聚催化性能

龚畅, 罗学刚, 张建平

现代化工 ›› 2018, Vol. 38 ›› Issue (4) : 68 -72.

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现代化工 ›› 2018, Vol. 38 ›› Issue (4) : 68-72. DOI: 10.16606/j.cnki.issn0253-4320.2018.04.016
科研与开发

介孔ZSM-5负载Ni催化剂的制备及乙烯齐聚催化性能

    龚畅, 罗学刚, 张建平
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Preparation of Ni catalyst supported by mesoporous ZSM-5 and its catalytic performance in ethylene oligomerization

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摘要

通过水热合成法和离子交换法制备了负载Ni的介孔Ni-HZSM-5分子筛催化剂,采用XRD、SEM、EDX、FT-IR、N2物理吸附-脱附等手段对催化剂组成、结构和形貌进行了研究,并以固定床微石英管反应器考察了不同反应温度、空速条件下介孔Ni-HZSM-5分子筛催化剂的乙烯齐聚反应性能。结果表明,Ni-HZSM-5样品具有介孔ZSM-5分子筛典型的特征结构,Ni进入分子筛骨架致使比表面降低,但孔径变大,更有利于齐聚反应的进行;在气体空速为1.2 L/(g·h)、反应温度为275℃时,乙烯的转化率为87.82%,C4的选择性可达57.25%,C6的选择性可达30.74%,说明Ni-HZSM-5催化剂对乙烯齐聚具有较好的催化性能。

Abstract

The Ni-supporting mesoporous Ni-HZSM-5 molecular sieve catalyst is synthesized by using hydrothermal synthesis and ion exchange methods.The composition,structure and morphology of prepared catalyst are investigated by XRD,SEM,EDX,FT-IR and N2 adsorption-desorption.The reaction performance of ethylene oligomerization over the prepared Ni-HZSM-5 molecular sieve catalyst is studied under different reaction temperatures and gas hourly space velocities (GHSV) in a fixed bed microquartz tube reactor.The results show that Ni-HZSM-5 samples have the same typical characteristic structure as mesoporous ZSM-5 molecular sieve.The specific surface area reduces slightly and pore size expands as Ni atoms embed in sieve frameworks,which is benefit to oligomerization.The conversion rate of ethylene can reach 87.82% with the selectivity rates of C4 and C6 being 57.25% and 30.74%,respectively under conditions that GHSV is 1.2 L/(g·h) and reaction temperature is 275℃.In summary,Ni-HZSM-5 catalyst has high catalytic performance for ethylene oligomerization.

关键词

水热合成法 / 催化剂 / 乙烯齐聚 / Ni-HZSM-5 / 离子交换法

Key words

hydrothermal synthesis method / catalyst / ethylene oligomerization / Ni-HZSM-5 / ion exchange method

Author summay

龚畅(1992-),男,硕士研究生,主要研究方向为齐聚催化剂的制备,gcwit2015@163.com

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介孔ZSM-5负载Ni催化剂的制备及乙烯齐聚催化性能[J]. , 2018, 38(4): 68-72 DOI:10.16606/j.cnki.issn0253-4320.2018.04.016

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