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author:

Si, Ruiru (Si, Ruiru.) [1] | Liu, Junfeng (Liu, Junfeng.) [2] | Yang, Kai (Yang, Kai.) [3] | Chen, Xun (Chen, Xun.) [4] (Scholars:陈旬) | Dai, Wenxin (Dai, Wenxin.) [5] (Scholars:戴文新) | Fu, Xianzhi (Fu, Xianzhi.) [6] (Scholars:付贤智)

Indexed by:

EI Scopus SCIE

Abstract:

The reaction behavior of CO over Au/TiO2 has been investigated by a temperature-programed surface reaction (TPSR) testing. We have found that there maybe existed four reaction processes of oxidizing CO over Au/TiO2 in the O-2-poor stream containing a trace H2O at or below 80 degrees C: (i) CO adsorbed at TiO2 sites is oxidized by H2O to form Ti-COOH species below 80 degrees C, which is desorbed into CO2 and H2O at 80 degrees C; (ii) CO adsorbed at Au sites is oxidized by H2O to form CO2; (iii) CO adsorbed at Au sites is oxidized by H2O to form H-2 and CO2 according to the water-gas shift reaction, which only occurs with the desorption of Ti-COOH species at TiO2 sites into CO2 at 80 degrees C; (iv) CO adsorbed at Au sites is oxidized by molecular O-2 to form CO2. For the three processes of H2O oxidizing CO, the chemisorption result of CO and O-2 over Au/TiO2 shows that it may be the Ti-bonded hydroxyl species (Ti OH) but not the adsorbed molecular H2O at TiO2 sites to react with CO adsorbed at Au or TiO2 sites. For the process of O-2 oxidizing CO, the non-promotion of pre-adsorption of O-2 on the formation of CO2 below 80 degrees C indicates that it may be the physisorbed molecular O-2 not the chemisorbed O-2 to directly react with CO adsorbed at Au sites. This work also indicates that the process of CO oxidation in the presence of H2O over the supported Au catalyst may be simultaneously oxidized by O-2 and H2O according to the respective process. (C) 2013 Elsevier Inc. All rights reserved.

Keyword:

Au/TiO2 CO oxidation Temperature-programed surface reaction (TPSR) Ti-bonded hydroxyl species

Community:

  • [ 1 ] [Si, Ruiru]Fuzhou Univ, State Key Lab Breeding Base, Fujian Prov Key Lab Photocatalysis, Res Inst Photocatalysis,Res Inst Photocatalysis, Fuzhou 350002, Peoples R China
  • [ 2 ] [Liu, Junfeng]Fuzhou Univ, State Key Lab Breeding Base, Fujian Prov Key Lab Photocatalysis, Res Inst Photocatalysis,Res Inst Photocatalysis, Fuzhou 350002, Peoples R China
  • [ 3 ] [Yang, Kai]Fuzhou Univ, State Key Lab Breeding Base, Fujian Prov Key Lab Photocatalysis, Res Inst Photocatalysis,Res Inst Photocatalysis, Fuzhou 350002, Peoples R China
  • [ 4 ] [Chen, Xun]Fuzhou Univ, State Key Lab Breeding Base, Fujian Prov Key Lab Photocatalysis, Res Inst Photocatalysis,Res Inst Photocatalysis, Fuzhou 350002, Peoples R China
  • [ 5 ] [Dai, Wenxin]Fuzhou Univ, State Key Lab Breeding Base, Fujian Prov Key Lab Photocatalysis, Res Inst Photocatalysis,Res Inst Photocatalysis, Fuzhou 350002, Peoples R China
  • [ 6 ] [Fu, Xianzhi]Fuzhou Univ, State Key Lab Breeding Base, Fujian Prov Key Lab Photocatalysis, Res Inst Photocatalysis,Res Inst Photocatalysis, Fuzhou 350002, Peoples R China

Reprint 's Address:

  • 戴文新

    [Dai, Wenxin]Fuzhou Univ, State Key Lab Breeding Base, Fujian Prov Key Lab Photocatalysis, Res Inst Photocatalysis,Res Inst Photocatalysis, Fuzhou 350002, Peoples R China

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Source :

JOURNAL OF CATALYSIS

ISSN: 0021-9517

Year: 2014

Volume: 311

Page: 71-79

6 . 9 2 1

JCR@2014

6 . 5 0 0

JCR@2023

ESI Discipline: CHEMISTRY;

ESI HC Threshold:268

JCR Journal Grade:1

CAS Journal Grade:1

Cited Count:

WoS CC Cited Count:

SCOPUS Cited Count:

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 0

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