沸石
乙烯
氢氧化物
化学
催化作用
氢氧化铝
多孔性
化学工程
BETA(编程语言)
无机化学
材料科学
铝
有机化学
计算机科学
工程类
程序设计语言
作者
Nazmul Abedin Khan,Dong Kyu Yoo,Biswa Nath Bhadra,Jong Won Jun,Tae‐Wan Kim,Chul‐Ung Kim,Sung Hwa Jhung
标识
DOI:10.1016/j.cej.2018.07.148
摘要
For the first time, beta zeolites (IZA code: BEA with 12-membered rings, having a wide range of SiO2/Al2O3) were converted into SSZ-13s (IZA code CHA, having 8-membered rings) in the presence of external silica source (here, Na2SiO3) and N,N,N-trimethyl-1-adamantanamine hydroxide as a structure directing agent. Na2SiO3 was essential for the successful conversion when the parent zeolite beta was Al-rich. The conversion of beta into SSZ-13 zeolite can be explained by the relative stabilities of beta and SSZ-13 zeolites, where pore size had more dominant role than the framework density. The obtained SSZ-13s were highly porous, had both weak and strong acidic sites and composed of tetrahedral aluminum. Finally, the synthesized SSZ-13s were applied in the direct conversion of ethylene-to-propylene (ETP) as a solid catalyst. The results showed that the SSZ-13s, converted from beta, were better or competitive in ETP (especially in the stable conversion of ethylene) against the SSZ-13 (synthesized by using tetraethylammonium hydroxide) that had showed very competitive performances earlier in ETP.
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