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作者:

Dong, Ning (Dong, Ning.) | Ye, Qing (Ye, Qing.) | Zhang, Dan (Zhang, Dan.) | Xiao, Yang (Xiao, Yang.) | Dai, Hongxing (Dai, Hongxing.) (学者:戴洪兴)

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EI Scopus SCIE

摘要:

The layered manganese oxide (S-MnO2)-supported reduced graphene oxide (rGO)-promoted silver catalysts (xAg-yrGO/delta-MnO2; x and y are the Ag and rGO contents (wt%), respectively) were prepared via a polyvinyl alcohol-protected reduction route. Physicochemical properties of these materials were determined using the numerous techniques, and their catalytic activities were evaluated for the oxidation of CO and ethyl acetate. It is found that the loading of rGO as an electron transfer promoter could significantly strengthen the metal-support interaction (SMSI) between Ag and delta-MnO2 and increase specific surface area of the sample, hence improving catalytic performance of the sample. Activity evaluation reveals that 1Ag-1.0rGO/delta-MnO2 showed the best catalytic activity and the lowest apparent activation energy (E-a), giving a T-90% of 140 degrees C and an E-a of 42.7 kJ/mol for CO oxidation, and a T-90% of 160 degrees C and an E-a of 39.8 kJ/mol for ethyl acetate oxidation at space velocity (SV) = 60,000 mL/(g h). The good performance of 1Ag-1.0rGO/S-MnO2 was associated with its high Mn3+/Mn4+ or O-ads/O-latt molar ratio, good low-temperature reducibility, and strong SMSI between Ag and delta-MnO2. The in situ DRIFTS characterization demonstrates that the carbonate and acetate species were the main intermediate products in CO and ethyl acetate oxidation over 1Ag-1.0rGO/delta-MnO2, respectively. The 1Ag-1.0rGO/delta-MnO2 sample was not significantly altered in physicochemical property after 55 h of stability test, but its activity decreased in the presence of water vapor, especially such an effect on ethyl acetate oxidation was more obvious, which was possibly due to the competitive adsorption of water and reactants on the catalyst surface.

关键词:

Carbon monoxide oxidation Manganese oxide-supported silver catalyst Reduced graphene oxide promoter Ethyl acetate oxidation Reaction mechanism

作者机构:

  • [ 1 ] [Dong, Ning]Beijing Univ Technol, Fac Environm & Life, Sch Environm & Chem Engn, Dept Environm Sci,Key Lab Beijing Reg Air Pollut, Beijing 100124, Peoples R China
  • [ 2 ] [Ye, Qing]Beijing Univ Technol, Fac Environm & Life, Sch Environm & Chem Engn, Dept Environm Sci,Key Lab Beijing Reg Air Pollut, Beijing 100124, Peoples R China
  • [ 3 ] [Zhang, Dan]Beijing Univ Technol, Fac Environm & Life, Sch Environm & Chem Engn, Dept Environm Sci,Key Lab Beijing Reg Air Pollut, Beijing 100124, Peoples R China
  • [ 4 ] [Xiao, Yang]Beijing Univ Technol, Fac Environm & Life, Sch Environm & Chem Engn, Dept Environm Sci,Key Lab Beijing Reg Air Pollut, Beijing 100124, Peoples R China
  • [ 5 ] [Dai, Hongxing]Educ Minist China, Key Lab Beijing Reg Air Pollut Control, Key Lab Adv Funct Mat, Beijing Key Lab Green Catalysis & Separat, Beijing 100124, Peoples R China
  • [ 6 ] [Dai, Hongxing]Beijing Univ Technol, Fac Environm & Life, Sch Environm & Chem Engn, Dept Environm Chem Engn,Lab Catalysis Chem & Nano, Beijing 100124, Peoples R China

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来源 :

JOURNAL OF HAZARDOUS MATERIALS

ISSN: 0304-3894

年份: 2022

卷: 431

1 3 . 6

JCR@2022

1 3 . 6 0 0

JCR@2022

ESI学科: ENGINEERING;

ESI高被引阀值:49

JCR分区:1

中科院分区:1

被引次数:

WoS核心集被引频次: 21

SCOPUS被引频次: 22

ESI高被引论文在榜: 0 展开所有

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