沸石
ZSM-5型
芳构化
开裂
化学
焦炭
催化裂化
布朗斯特德-洛瑞酸碱理论
乙烯
选择性
路易斯酸
轻质原油
催化作用
有机化学
无机化学
化学工程
工程类
作者
Qingjing Niu,Lisha Wei,Ruifeng Hou,Ling Zhang,Kun Hao,Caixia Hu,Xiaodong Wen,Hongwei Xiang,Zhichao Tao,Yong Yang,Yongwang Li
出处
期刊:Fuel
[Elsevier]
日期:2023-07-25
卷期号:353: 129255-129255
被引量:6
标识
DOI:10.1016/j.fuel.2023.129255
摘要
The three dimension (3D) 10-membered ring channels zeolite has a unique advantage in increasing light olefins for catalytic cracking reaction. Herein, zeolites IM-5, ZSM-5 and ZSM-11 were synthesized hydrothermally to achieve comparable texture properties and SiO2/Al2O3 ratios. The acid content and acid strength of the three zeolites were as follows: IM-5 > ZSM-5 > ZSM-11. Meanwhile, 1H DQ MAS NMR confirmed that there was a synergistic effect between Brønsted and Lewis acids in IM-5 zeolite. However, IM-5 zeolite with lots of strong BAS had an unexpected low TOF in n-heptane cracking. Furthermore, the light olefins selectivity was as follows: IM-5 > ZSM-11 > ZSM-5 at 550–650 ℃ in the absence of steam. IM-5 zeolite had the particular advantage in ethylene, and its selectivity was up to 44.9 %. After steam was introduced, the monomolecular cracking reaction, the aromatization of propylene and the deep cracking of C3 and C4 hydrocarbons were inhibited over the three zeolites. Steam could prolong the activity of IM-5 zeolite, but accelerate the deactivation of ZSM-5 and ZSM-11 zeolites. The primary cause for the rapid deactivation of ZSM-5 and ZSM-11 zeolites was dealuminization in steam, whereas for the IM-5 zeolite, it was the rapid formation of coke on its surface, thereby blocking its micropore channels.
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