Insight into the effect of mass transfer channels and intrinsic reactivity in titanium silicalite catalyst for one-step epoxidation of propylene

被引:10
作者
Jie, Zhiyuan [1 ]
Yang, Tengfei [1 ]
Wang, Xiaobin [1 ]
Ji, Yun [1 ]
Li, Yuchao [1 ]
Meng, Bo [1 ]
Tan, Xiaoyao [2 ]
Liu, Shaomin [3 ]
机构
[1] Shandong Univ Technol, Sch Chem & Chem Engn, Zibo 255000, Peoples R China
[2] Tianjin Polytech Univ, Dept Chem Engn, Tianjin 300387, Peoples R China
[3] Beijing Univ Chem Technol, Coll Chem Engn, State Key Lab Organ Inorgan Composites, Beijing 100029, Peoples R China
关键词
Propylene epoxidation; TS-1; Mass transfer channels; Acidic sites; Ti species; GAS-PHASE EPOXIDATION; HIERARCHICAL TS-1; HYDROGEN-PEROXIDE; BENZENE HYDROXYLATION; TI SITES; RECRYSTALLIZATION; H2O2; PERFORMANCE; PARTICLES; ZEOLITES;
D O I
10.1016/j.surfin.2022.101741
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
One-step epoxidation of propylene to propylene oxide (PO) in TS-1/H2O2 system is a promising green and sustainable formation route. However, the TS-1 catalyst is limited by the small pore channels and inadequate intrinsic reactivity. Herein, tetrapropylammonium hydroxide (TPAOH) is used to modify the TS-1 skeleton structures to improve the mass transfer and intrinsic reactivity. Comparative catalytic performance tests indicate that the optimized temperature for TPAOH treatment to modify TS-1 was 90 degrees C, and the achieved H(2)O2 utilization efficiency and the PO selectivity can be over 80%. Different TPAOH treatment temperatures significantly influenced the dissolution and recrystallization behavior of TS-1, which altered the composition and microstructure in terms of the pore volume and size, surface properties, and active sites. Our findings indicated that the enlarged pore channels for favorable mass transfer, improved hydrophobic surfaces, enriched framework titanium, and reduced acid strength of titanium silicalite zeolite should be the primary reasons for the enhanced conversion and yields.
引用
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页数:9
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