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The effect of cerium incorporation on the catalytic performance of cobalt and manganese containing layer double oxides for acetone oxidation

Authors :
Zhao, Qian
Liu, Qingling
Han, Jinfeng
Lu, Shuangchun
Su, Yun
Song, Chunfeng
Ji, Na
Lu, Xuebin
Ma, Degang
Cheung, Ocean
Zhao, Qian
Liu, Qingling
Han, Jinfeng
Lu, Shuangchun
Su, Yun
Song, Chunfeng
Ji, Na
Lu, Xuebin
Ma, Degang
Cheung, Ocean
Publication Year :
2019

Abstract

BACKGROUND Acetone is a volatile organic compound (VOC) that is often associated with poor air quality. Acetone has chronic toxicity towards humans and has significant impact to the overall atmospheric air quality. In this study, several layer double oxides (with M2+ = Mg, Ni, Co or Mn and M3+= Al or Ce)were tested as catalyst in acetone oxidation. RESULTS MnAl-LDO was found to be the most efficient catalyst. 50% acetone conversion was achieved at 170 °C (T50%) and 90% conversion at 200 °C (T90%).The incorporation of Ce on MnCeAl-LDO did not improve its catalytic properties over MnAl-LDO (the T50% for MnCeAl-LDO was 12 °C higher than for MnAl-LDO). The good performance on MnAl-LDO was due to the presence of Mn3+. MnAl-LDO was not affect when water was introduced into the catalytic reaction setup. Less than 5 % fluctuation in the acetone conversion rate at 170 and 200 °C was detected in the presence of 5.5% water. The incorporation of Ce on CoCeAl-LDO improved its catalytic performance over CoAl-LDO (T50% of CoCeAl-LDO was 15 °C lower than CoAl-LDO).Our results showed that the good catalytic performance of CoCeAl-LDO was ascribed to the increased Co2+/Co3+ ratio and the abundance of lattice oxygen (Olatt). CONCLUSION MnAl-LDO has good catalytic properties for acetone oxidation, even under humid conditions. The LDO catalysts tested here can be developed into efficient catalysts for acetone oxidation and serve as functional materials for the reduction in acetone or VOC emission. This article is protected by copyright. All rights reserved.

Details

Database :
OAIster
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1235235138
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.1002.jctb.5868