Overcoming the Deactivation of Pt/CNT by Introducing CeO2 for Selective Base-Free Glycerol-to-Glyceric Acid Oxidation

被引:65
|
作者
Zhang, Xueqiong [1 ]
Zhou, Dan [1 ]
Wang, Xiaojing [1 ]
Zhou, Jian [1 ]
Li, Jiefei [1 ]
Zhang, Mingkai [2 ]
Shen, Yihong [3 ]
Chu, Haibin [1 ]
Qu, Yongquan [2 ]
机构
[1] Inner Mongolia Univ, Coll Chem & Chem Engn, Inner Mongolia Engn & Technol Res Ctr Catalyt Con, Hohhot 010021, Peoples R China
[2] Xi An Jiao Tong Univ, Frontier Inst Sci & Technol, Xian 710049, Peoples R China
[3] PetroChina Petrochem Res Inst, Beijing 102206, Peoples R China
基金
中国国家自然科学基金;
关键词
heterogeneous catalysis; glycerol oxidation; platinum; catalyst deactivation; ceria; FREE AQUEOUS-SOLUTION; PT-CU CATALYSTS; PLATINUM CATALYSTS; AEROBIC OXIDATION; CARBON NANOTUBES; LACTIC-ACID; NANOPARTICLES; OXYGEN; TEMPERATURE; ALCOHOLS;
D O I
10.1021/acscatal.9b05559
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
Catalytic base-free oxidation of biomass-derived glycerol represents a promising approach for the value-added utilization of glycerol. However, the commonly used Pt/carbon nanotubes (Pt/CNT) catalysts suffer from the severe deactivation, because of the strong adsorption of glyceric acid (GLYA), resulting in the serious Pt-surface poisoning and their consequent poor activity with low selectivity toward GLYA. Here, we demonstrate that integrating CeO2 with Pt/CNT could effectively alleviate the catalyst deactivation, delivering high activity and selectivity to produce GLYA. The valence band analysis and kinetic experiments suggest that the Pt-CeO2/CNT ternary interface would weaken the GLYA adsorption on Pt and lower the energy barrier for glycerol oxidation. Moreover, via the generated OH* from H2O dissociation, CeO2 can promote the oxidation of primary hydroxyl groups of glycerol, leading to a high selectivity of GLYA.
引用
收藏
页码:3832 / 3837
页数:6
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