催化作用
开裂
化学
焦炭
催化裂化
吡啶
聚乙烯
癸烷
聚丙烯
沸石
化学工程
蒸馏
微型多孔材料
有机化学
无机化学
工程类
作者
Karolina A. Tarach,Joaquı́n Martı́nez-Triguero,Susana Valencia,Kamila Wojciechowska,Fernando Rey,Kinga Góra‐Marek
标识
DOI:10.1016/j.apcatb.2023.123066
摘要
The 10-ring zeolites TNU-9 and IM-5 were obtained by a desilication and evaluated in series of acid-catalysed cracking reactions. n-Decane and 1,3,5-tri-iso-propylbenzene cracking were performed as model reactions, while vacuum gas oil, polypropylene and polyethylene were cracked into add-value lower molecular weight chemicals. The catalytic performance improvement of hierarchical zeolites was rationalized by deep acid sites characterization in situ FT-IR studies of pyridine, carbon monoxide and 2,6-di-tert-butylpyridine sorption. Further, operando FT-IR-GC studies supported by 2D COS (two-dimensional correlation) analysis provided insight into cracking and coking of catalysts during polypropylene and polyethylene decomposition. It was found that NaOH-derived catalysts ensure the most usurped acidity, in terms of number and accessibility of the sites, and then with better performance. In VGO cracking the connected mesopores added post-synthesis increased yields to propylene and middle distillates and lowered coke production. A bigger share of iso-olefins was observed both in VGO and polyolefins cracking products.
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