首页 | 本学科首页   官方微博 | 高级检索  
     

分子筛催化异丁烷与正丁烯烷基化反应性能
引用本文:王新星,钱小磊,孙晶明,崔楼伟,顾建峰. 分子筛催化异丁烷与正丁烯烷基化反应性能[J]. 工业催化, 2017, 25(1): 61-65
作者姓名:王新星  钱小磊  孙晶明  崔楼伟  顾建峰
作者单位:西安元创化工科技股份有限公司,陕西 西安 710061
基金项目:陕西省工业科技攻关项目(批准号2015GY151)
摘    要:
以Y、β、MCM-41和EU-1分子筛为活性组分制备异丁烷与正丁烯烷基化反应催化剂,并利用NH_3-TPD和N_2物理吸附-脱附对催化剂进行表征。结果表明,HY分子筛催化剂的总酸量最大,MCM-41分子筛催化剂的总酸量最小,Hβ和HEU-1分子筛催化剂总酸量适中,Hβ分子筛催化剂平均孔径最大,而大孔径有利于分子扩散。对分子筛催化异丁烷与正丁烯反应的催化性能进行研究,结果表明,Hβ分子筛催化剂的失活速率最低,正丁烯异构化率最低,生成的烷基化油辛烷值达85.2,对Hβ分子筛催化剂进行Pt元素改性后催化剂的失活速率降低。

关 键 词:石油化学工程  异丁烷与正丁烯烷基化反应  β分子筛  分子筛催化剂  

Catalytic performance of molecular sieve catalysts for alkylation of isobutane and 1-butene
Wang Xinxing,Qian Xiaolei,Sun Jingming,Cui Louwei,Gu Jianfeng. Catalytic performance of molecular sieve catalysts for alkylation of isobutane and 1-butene[J]. Industrial Catalysis, 2017, 25(1): 61-65
Authors:Wang Xinxing  Qian Xiaolei  Sun Jingming  Cui Louwei  Gu Jianfeng
Affiliation:Xi’an Origin Chemical Technologles Co.,Ltd.,Xi’an 710061,Shaanxi,China
Abstract:
Alkylation catalysts were prepared by using Y,β,MCM-41 and EU-1 molecular sieves and were characterized by means of NH3-TPD and N2 physical adsorption-desorption.The results showed that the total acid amount of HY molecular sieve catalyst was maximum,the total acid amount of MCM-41 molecular sieve catalyst was minimum,and the total acid amounts of Hβ and HEU-1 molecular sieves were moderate.Hβ molecular sieve catalyst possessed maximum average aperture,which was conducive to molecular diffusion.The effects of molecular sieve catalyst for isobutane and 1-butene reaction were investigated.The results showed that Hβ molecular sieve catalyst possessed the lowest deactivation rate and the lowest isomerization rate of 1-butene,and the octane value of alkylated oil reached 85.2.The deactivation rate of Hβ molecular sieve catalyst after modification by Pt was reduced.
Keywords:petrochemical engineering  isobutene/1-butene alkylation  β-molecular sieve  molecular sieve catalyst  
本文献已被 CNKI 等数据库收录!
点击此处可从《工业催化》浏览原始摘要信息
点击此处可从《工业催化》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号