Titanium-rich TS-1 zeolite for highly efficient oxidative desulfurization

被引:27
|
作者
Bai, Risheng [1 ,2 ]
Song, Yue [1 ]
Tian, Ge [1 ]
Wang, Fei [3 ]
Corma, Avelino [2 ]
Yu, Jihong [1 ,4 ]
机构
[1] Jilin Univ, Coll Chem, State Key Lab Inorgan Synth & Preparat Chem, Changchun 130012, Peoples R China
[2] Univ Politecn Valencia, CSIC, Inst Tecnol Quim, Valencia 46022, Spain
[3] Jilin Univ, State Key Lab Superhard Mat, Changchun 130012, Peoples R China
[4] Jilin Univ, Int Ctr Future Sci, Changchun 130012, Peoples R China
基金
欧洲研究理事会; 中国国家自然科学基金;
关键词
TS-1; Zeolite; Ti-rich; Heterogeneous catalysis; Oxidative desulfurization; CATALYTIC PERFORMANCE; EPOXIDATION; TI; SITES; BETA; CRYSTALLIZATION; SILICALITE-1; REACTIVITY; STATE; FUEL;
D O I
10.1016/j.gee.2021.03.006
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
The exploration of highly efficient catalysts based on nano-sized Ti-rich titanosilicate zeolites with controllable active titanium species is of great importance in zeolite catalytic reactions. Herein, we reported an efficient and facile synthesis of nano-sized Ti-rich TS-1 (MFI) zeolites by replacing tetrabutyl orthotitanate (TBOT) with tetrabutyl orthotitanate tetramer (TBOT-tetramer) as the titanium source. The introduced TBOT-tetramer slowed down the zeolite crystallization process, and accordingly balanced the rate of incorporating Ti and the crystal growth and inhibited the massive formation of anatase species. Notably, the prepared Ti-rich TS-1 zeolite sample had a Si/Ti as low as 27.6 in contrast to conventional one with a molar ratio of 40. The TBOT-tetramer endowed the titanosilicate zeolites with enriched active titanium species and enlarged external surface area. It also impeded the formation of anatase species, resulting in superior catalytic behavior toward the oxidative desulfurization of dibenzothiophene compared with the conventional TS-1 zeolite counterpart prepared with TBOT.(c) 2021 Institute of Process Engineering, Chinese Academy of Sciences. Publishing services by Elsevier B.V. on behalf of KeAi Com-munications Co., Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:163 / 172
页数:10
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