Rapid Synthesis of Self-Pillared ZSM-5 Zeolite Nanosheets with Enhanced Catalytic Performance in n-Octane Cracking

被引:1
作者
Wang, Peng [1 ]
Wang, Jianjie [1 ]
Shu, Xiaolong [1 ]
Bian, Mengqi [1 ]
Xiao, Xia [1 ]
Fan, Xiaoqiang [1 ]
Kong, Lian [1 ]
Xie, Zean [1 ]
Zhao, Zhen [1 ,2 ]
机构
[1] Shenyang Normal Univ, Inst Catalysis Energy & Environm, Coll Chem & Chem Engn, Shenyang 110034, Peoples R China
[2] China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China
基金
中国国家自然科学基金;
关键词
REACTION PATHWAYS; PENTANE CRACKING; ACID SITES; HEPTANE; ADSORPTION; MFI;
D O I
10.1021/acs.iecr.4c02530
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Investigating the synthesis of hierarchical ZSM-5 zeolite and its catalytic performance in the catalytic cracking of n-octane is significant for industrial production. In this work, self-pillared ZSM-5 zeolite nanosheets were prepared using a seed-assisted crystallization approach. The influence of crystallization time on the relative crystallinity, morphologies, pore characteristics, and acidity of a series of nanosheet-stacked ZSM-5 zeolite was investigated by using XRD, Raman, FT-IR, SEM, TEM, nitrogen physisorption, 27Al MAS NMR, NH3-TPD, and Py-IR characterization techniques. The self-pillared ZSM-5 zeolite synthesized with a crystallization time of 8 h exhibited enhanced catalytic performance in terms of both conversion and light olefin selectivity during n-octane cracking, which could be attributed to the synergistic effect of a suitable mesoporous structure and moderate acidity. Furthermore, the hierarchical self-pillared ZSM-5 zeolite exhibited improved anticoking stability because the shortened straight channel lengths can efficiently suppress the aromatic-based cycle, thus hindering the accumulation of the polycyclic aromatics.
引用
收藏
页码:18773 / 18782
页数:10
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