酸性调控对1-己烯临氢异构化反应性能的影响

刘蕾, 赵新红, 姚文君, 张文奇, 向永生

现代化工 ›› 2022, Vol. 42 ›› Issue (11) : 93 -99.

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现代化工 ›› 2022, Vol. 42 ›› Issue (11) : 93-99. DOI: 10.16606/j.cnki.issn0253-4320.2022.11.018
科研与开发

酸性调控对1-己烯临氢异构化反应性能的影响

    刘蕾, 赵新红, 姚文君, 张文奇, 向永生
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Effect of acidity control on performance of 1-hexene hydro-isomerization reaction

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摘要

以无定形酸性硅铝材料ASA30和ZSM-35沸石为母体材料,通过复配制备了一系列组成不同的复合催化材料,并考察了其在1-己烯临氢异构化反应中的催化性能。利用N2物理吸-脱附、NH3-TPD和Py-IR等对复合催化材料的孔结构和酸性质进行研究。结果表明,复合催化剂的孔结构参数、酸类型、酸强度及强弱酸酸量随其组成发生有规律的变化。骨架异构化率及异构烷烃选择性最好的AZ-3/2在250℃就达到其最优异构化性能,骨架异构化率为84.81%,异构烷烃选择性为27.53%,异构烯烃选择性为57.28%,正构烷烃选择性仅为4.65%。此时L/B酸比例为2.3、中强酸/弱酸比例为5.26。

Abstract

ASA30 zeolite and ZSM-35 zeolite,both amorphous acidic silica-alumina materials,are used as parent materials,a series of composite catalytic material with different compositions are prepared via compounding method,and their catalytic performance in the hydro-isomerization of 1-hexene is investigated.The pore structure and acidic properties of the composite catalytic material are studied by means of N2 physical adsorption-desorption,NH3-TPD and Py-IR.The results show that the pore structure parameters,acid type,acid strength and the amounts of strong and weak acids of the composite catalyst change regularly with its composition.AZ-3/2 composite catalyst with the best skeletal isomerization rate and iso-alkanes selectivity can reach its optimal isomerization performance at 250℃,over which the skeletal isomerization rate of 1-hexene reaches 84.81%,the selectivity of iso-alkanes is 27.53%,the selectivity of iso-olefins is 57.28%,and the selectivity of n-alkanes is 4.65%.The ratio of L acid to B acid of AZ-3/2 is 2.3,and the ratio of medium strong acid to weak acid is 5.26.

关键词

烯烃临氢异构化反应 / 骨架异构烷烃 / 烯烃骨架异构 / ZSM-35 / 酸性硅铝材料

Key words

hydro-isomerization of olefins / skeletal iso-alkanes / skeletal isomerization of olefins / ZSM-35 / acidic silica-alumina materials

Author summay

刘蕾(1990-),女,硕士研究生,主要从事酸性材料改性及其临氢异构化性能研究,2547523110@qq.com

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酸性调控对1-己烯临氢异构化反应性能的影响[J]. , 2022, 42(11): 93-99 DOI:10.16606/j.cnki.issn0253-4320.2022.11.018

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