Oxidation of Dichloromethane over Au, Pt, and Pt-Au Containing Catalysts Supported on γ-Al2O3 and CeO2-Al2O3

被引:7
|
作者
Nevanpera, Tuomas K. [1 ]
Pitkaaho, Satu [1 ]
Ojala, Satu [1 ]
Keiski, Riitta L. [1 ]
机构
[1] Univ Oulu, Fac Technol Environm & Chem Engn, POB 4300, FI-90014 Oulu, Finland
来源
MOLECULES | 2020年 / 25卷 / 20期
关键词
environmental catalysis; gold; platinum; bimetallic catalyst; chlorinated volatile organic compound (CVOC); VOLATILE ORGANIC-COMPOUNDS; CHLORINATED HYDROCARBONS; GOLD CATALYSTS; PERCHLOROETHYLENE-ACTIVITY; ZEOLITE CATALYSTS; OXIDE CATALYSTS; CO OXIDATION; DESTRUCTION; METHANOL; PD;
D O I
10.3390/molecules25204644
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Au, Pt, and Pt-Au catalysts supported on Al2O3 and CeO2-Al2O3 were studied in the oxidation of dichloromethane (DCM, CH2Cl2). High DCM oxidation activities and HCl selectivities were seen with all the catalysts. With the addition of Au, remarkably lower light-off temperatures were observed as they were reduced by 70 and 85 degrees with the Al2O3-supported and by 35 and 40 degrees with the CeO2-Al2O3-supported catalysts. Excellent HCl selectivities close to 100% were achieved with the Au/Al2O3 and Pt-Au/Al2O3 catalysts. The addition of ceria on alumina decreased the total acidity of these catalysts, resulting in lower performance. The 100-h stability test showed that the Pt-Au/Al2O3 catalyst was active and durable, but the selectivity towards the total oxidation products needs improvement. The results suggest that, with the Au-containing Al2O3-supported catalysts, DCM decomposition mainly occurs via direct DCM hydrolysis into formaldehyde and HCl followed by the oxidation of formaldehyde into CO and CO2.
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页数:25
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