A Nonoxide Catalyst System Study: Alkali Metal-Promoted Pt/AC Catalyst for Formaldehyde Oxidation at Ambient Temperature

被引:69
|
作者
Wang, Chunying [1 ,2 ]
Li, Yaobin [1 ,2 ,3 ]
Zheng, Lirong [4 ]
Zhang, Changbin [2 ,5 ]
Wang, Yin [1 ]
Shan, Wenpo [1 ,3 ]
Liu, Fudong [6 ]
He, Hong [2 ,7 ,8 ]
机构
[1] Chinese Acad Sci, Ctr Excellence Reg Atmospher Environm, Key Lab Urban Pollutant Convers, Inst Urban Environm, Xiamen 361021, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Chinese Acad Sci, Zhejiang Key Lab Urban Environm Proc & Pollut Con, Ningbo Urban Environm Observat & Res Stn, Ningbo 315800, Peoples R China
[4] Chinese Acad Sci, Inst High Energy Phys, Beijing Synchrotron Radiat Facil, Beijing 100049, Peoples R China
[5] Chinese Acad Sci, State Key Joint Lab Environm Simulat & Pollut Con, Res Ctr Ecoenvironm Sci, Beijing 100085, Peoples R China
[6] Univ Cent Florida, Dept Civil Environm & Construct Engn CECE, Catalysis Cluster Renewable Energy & Chem Transfo, NanoSci Technol Ctr NSTC, Orlando, FL 32816 USA
[7] Chinese Acad Sci, State Key Joint Lab Environm Simulat & Pollut Con, Res Ctr Ecoenvironm Sci, Ningbo Urban Environm Observat & Res Stn, Beijing 100085, Peoples R China
[8] Chinese Acad Sci, Zhejiang Key Lab Urban Environm Proc & Pollut Con, Ningbo Urban Environm Observat & Res Stn, Beijing 100085, Peoples R China
基金
中国国家自然科学基金;
关键词
formaldehyde; alkali metal; activated carbon; surface hydroxyl; catalytic oxidation; WATER-GAS SHIFT; ROOM-TEMPERATURE; AIRBORNE FORMALDEHYDE; SUPPORT INTERACTION; PD/TIO2; CATALYST; CO OXIDATION; REMOVAL; HCHO; MINERALIZATION; FACILITATE;
D O I
10.1021/acscatal.0c03196
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
Metal oxides have been extensively used as supports in noble metal-based catalysts for formaldehyde (HCHO) oxidation, utilizing the benefit of the strong metal-support interaction (SMSI). Non-oxide supported noble metal catalysts are still rarely investigated in the field of HCHO oxidation. Herein, a series of Pt catalysts supported on a nonoxide, that is, activated carbon (AC), were studied in detail. Pt/AC catalysts with or without addition of the alkali metal Na were prepared and tested for HCHO oxidation. HCHO could be completely oxidized to form H2O and CO2 at 25 degrees C on the Na-Pt/AC-R (reduced Na-Pt/AC) catalyst, but in contrast, the Pt/AC-R catalyst only achieved 40% HCHO conversion under the same reaction conditions. The characterization results indicated that Na addition to the Na-Pt/AC-R catalyst could induce the formation of Pt-O-x-Na species, which improves the stability of Pt species, increases Pt dispersion, and enhances the activation of chemisorbed oxygen and water to form abundant surface-active hydroxyl groups. Meanwhile, HCHO-TPD confirmed that HCHO could be transformed into CO2 and H2O directly because of the presence of abundant OH groups on the Na-Pt/AC-R catalyst. In this study, the promotion effect of alkali metals on supported Pt catalysts for HCHO oxidation was further extended to a catalyst system with a nonoxide carrier.
引用
收藏
页码:456 / 465
页数:10
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