聚丙烯
开裂
机制(生物学)
离子交换
催化裂化
化学工程
离子
材料科学
化学
复合材料
有机化学
工程类
认识论
哲学
作者
Xue Yang,Boxu Gao,Wanyi Li,Kaige Hou,Kexin Yan,Tianlan Yan,Sinong Wang,Yahong Zhang,Lei Wang,Yi Tang
出处
期刊:Chem catalysis
[Elsevier]
日期:2024-03-01
卷期号:4 (3): 100947-100947
标识
DOI:10.1016/j.checat.2024.100947
摘要
Precisely tailoring the location and strength of Brønsted acid is crucial for the catalytic cracking of polyolefins. Here, by simple sodium cation exchange (xNa-USY, where x is the Na/Al ratio), it was unexpectedly discovered that xNa-USY (x < 0.5) displayed a lower cracking temperature of polypropylene (PP) with optimum performance and excellent reproducibility at x = 0.38, rather than pure H-USY, as generally believed. Combining spectroscopic and microstructural characterizations, a putative mechanism was proposed from the perspective of proton location and acid strength. When lacking strong Brønsted acid near site II, PP tended to cleave into longer alkane fractions at low temperatures and volatilized directly, exhibiting significant apparent cracking capacity. Meanwhile, the lower distribution of olefins and aromatics remarkably reduced coke generation at high temperatures. These findings not only shed light on the optimization of plastic degradation catalysts but also expand our knowledge of the zeolitic acid-catalyzed cracking process.
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