Interfacial synergism of hollow mesoporous Pt/WOx/SiO2-TiO2 catalysts enable highly selective hydrogenolysis of glycerol to 1,3-propanediol

被引:4
|
作者
Chen, Yan
Zeng, Yang
Hung, Chin-Te
Zhang, Zhenghao
Lv, Zirui
Huang, Senchuan
Yang, Yi
Liu, Yupu
Li, Wei [1 ]
机构
[1] Fudan Univ, State Key Lab Mol Engn Polymers, Dept Chem, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
hollow nanospheres; mesoporous materials; Pt/WOx/SiO2-TiO2; catalysts; selective hydrogenolysis of glycerol; 1; 3-propanediol; TUNGSTEN-OXIDE; TIO2; WOX; NANOPARTICLES; PERFORMANCE; GRAPHENE; STRATEGY;
D O I
10.1007/s12274-023-5712-0
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 selective hydrogenolysis of glycerol exhibits great prospects, while the catalysts with high selectivity and activity are still missing and need to be created urgently. Herein, we report the synthesis of hollow mesoporous Pt/WOxSiO2-TiO2 nanosphere catalysts with bi-functional interfaces synergistically for high efficiency conversion of glycerol to 1,3-propanediol. The hollow mesoporous Pt/WOxSiO2-TiO2 catalysts show a typical brick-concrete liked framework with a high surface area (179.3 m(2)g(.1)), large mesopore size (10.6 nm), uniform particle size (similar to 400 nm), and ultrathin shell thickness (similar to 75 nm). The brick anatase nanocrystals and concrete amorphous SiO2 networks can selectively rivet Pt nanoparticles and WOx nanocluster species, respectively, thus constructing two interfaces for effective adsorption, rapidly catalytic dehydration and hydrogenation processes. The hollow mesoporous Pt/WOxSiO2-TiO2 catalysts deliver a high selectivity of 53.8% for 1,3-propanediol (1,3-PDO) at a very high glycerol conversion of 85.0%. As a result, a favorable 1,3-PDO yield of 45.7% can be obtained with excellent stability, which is among the best performances of previously reported catalysts. This work paves a new way to synthesize catalysts with high selectivity, high activity and high stability.
引用
收藏
页码:9081 / 9090
页数:10
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