Pt-Pd bimetallic nanoparticles anchored on uniform mesoporous MnO2 sphere as an advanced nanocatalyst for highly efficient toluene oxidation

被引:29
作者
He, Jiaqin [1 ]
Chen, Dongyun [1 ]
Li, Najun [1 ]
Xu, Qingfeng [1 ]
Li, Hua [1 ]
He, Jinghui [1 ]
Lu, Jianmei [1 ]
机构
[1] Soochow Univ, Collaborat Innovat Ctr Suzhou Nano Sci & Technol, Coll Chem, Chem Engn & Mat Sci, Suzhou 215123, Jiangsu, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
MnO2; nanospheres; Mesoporous structure; Pt-Pd bimetal; VOCs oxidation; CATALYTIC COMBUSTION; OXIDE CATALYSTS; MANGANESE OXIDE; PERFORMANCE; NI; CO; REMOVAL; FORMALDEHYDE; SUBSTITUTION; STABILITY;
D O I
10.1016/j.gee.2021.03.002
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
Improving catalytic performance is a yet still challenge in thermal catalytic oxidation. Herein, uniform mesoporous MnO2 nanosphere-supported bimetallic Pt-Pd nanoparticles were successfully fabricated via a SiO2 template strategy for the total catalytic degradation of volatile organic compounds at low temperature. The introduction of mesopores into the MnO2 support induces a large specific surface area and pore size, thus providing numerous accessible active sites and enhanced diffusion properties. Moreover, the addition of a secondary noble metal can adjust the O-ads/O-latt molar ratios, resulting in high catalytic activity. Among them, the catalyst having a Pt/Pd molar ratio of 7:3 exhibits optimized catalytic activity at a weight hourly space velocity of 36,000 mL g(-1) h(-1), reaching 100% toluene oxidation at 175 degrees C with a lower activation energy (57.0 kJ mol(-1)) than the corresponding monometallic Pt or non-Pt-based catalysts (93.8 kJ mol(-1) and 214.2 kJ mol(-1)). Our findings demonstrate that the uniform mesoporous MnO2 nanosphere-supported bimetallic Pt-Pd nanoparticles catalyst is an effective candidate for application in elimination of toluene. (c) 2021 Institute of Process Engineering, Chinese Academy of Sciences. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co., Ltd.
引用
收藏
页码:1349 / 1360
页数:12
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