A comparative synthesis of ZSM-5 with ethanol or TPABr template: distinction of Brønsted/Lewis acidity ratio and its impact on n-hexane cracking

CATALYSIS SCIENCE & TECHNOLOGY(2018)

引用 34|浏览5
暂无评分
摘要
Two kinds of ZSM-5 zeolites with various SiO2/Al2O3 ratios were synthesized using ethanol (EtOH) or tetrapropylammonium bromide (TPABr) as the template respectively and their physicochemical properties were investigated extensively. Different ZSM-5 morphologies were observed for each kind of sample, the former with coffin-shaped single crystals and the latter with aggregates assembled from nanocrystals. The desilication process occurred and intensified at a later period of crystallization for ZSM-5 by EtOH with increasing SiO2/Al2O3 ratio and/or increasing alkalinity, due to its weaker pore-filling effect. Specifically, ZSM-5 zeolites by EtOH had a large amount of Bronsted acid sites (BAS) and a much less amount of Lewis acid sites (LAS), leading to an ultra-high B/L ratio (45-66); while those by TPA(+) with comparable acidity possessed a usual B/L ratio (6-8). Owing to no octahedrally coordinated Al in both kinds of ZSM-5, the amount of LAS should be attributed to the tri-coordinated Al "defect" sites, in accordance with the extra silanols determined by OH-IR. Further, ZSM-5 by EtOH exhibited fewer internal defective Al sites, which was responsible for its small number of LAS. Applied to n-hexane cracking, the ZSM-5 zeolite by EtOH had high activity with twice the lifetime (60 vs. 35 h) compared to that by TPA(+) with a similar SiO2/Al2O3 ratio. The ratio of accumulated amount of coke to converted n-hexane was obtained as a measure of average coke selectivity (S-c). The ZSM-5 zeolites by EtOH displayed less than half the S-c value (0.45) in comparison with those by TPA(+) (1.08), due to the big difference in LAS, regardless of their SiO2/Al2O3 ratio, morphological structure and reaction conditions. Thus, for ZSM-5 possessing a high B/L ratio improves the catalytic activity and decreases coke deposit through suppressing the dehydrogenation process of the reaction intermediate to form coke precursor.
更多
查看译文
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要