• Complex
  • Title
  • Keyword
  • Abstract
  • Scholars
  • Journal
  • ISSN
  • Conference
成果搜索

author:

Vargheese, Vibin (Vargheese, Vibin.) [1] | Murakami, Junichi (Murakami, Junichi.) [2] | Bando, Kyoko K. (Bando, Kyoko K..) [3] | Ghampson, I. Tyrone (Ghampson, I. Tyrone.) [4] | Yun, Gwang-Nam (Yun, Gwang-Nam.) [5] | Kobayashi, Yasukazu (Kobayashi, Yasukazu.) [6] | Oyama, S. Ted (Oyama, S. Ted.) [7]

Indexed by:

EI Scopus SCIE

Abstract:

The direct partial oxidation of CH4 to dimethyl ether (DME) on a Pt/Y2O3 catalyst was studied using a mixture of NO and O-2 as the oxidant. The reaction was carried out in a fixed bed reactor at 0.1 MPa and 275-400 degrees C using 20% CH4, 1% NO, and 1% O-2 in inert gas. No methanol was detected in the effluent and a contact time study demonstrated that DME was a primary product. The DME productivities were comparable to the oxygenate (methanol, formaldehyde) productivities obtained with stronger oxidants such as N2O, H2O2, and O-3. The presence of Pt and the NO + O-2 gas mixture was necessary for DME formation; without NO only CO2 was produced. During the methane partial oxidation reaction NO and NO2 were not reduced to N-2, indicating that they worked as a shuttle to transfer oxygen from O-2 to CH4. In situ Fourier transform infrared showed the formation of a bridged nitrate species on the Pt/Y2O3 catalyst which was associated with the reaction of CH4. A comprehensive study of this bridged nitrate species indicated they were formed on yttria sites close to Pt and were likely responsible for the formation of DME. The characterization of catalysts using X-ray diffraction showed that the Pt was highly dispersed and CO uptake measurements indicated a particle size of similar to 3 nm. Analysis by X-ray absorption fine structure measurements showed the presence of Pt oxide with Pt-O and Pt-Pt bonds. (C) 2020 Elsevier Inc. All rights reserved.

Keyword:

CH4 partial oxidation Dimethyl ether In situ FTIR Nitrate species NO and O-2 XAFS

Community:

  • [ 1 ] [Oyama, S. Ted]Fuzhou Univ, Sch Chem Engn, Fuzhou 350116, Peoples R China
  • [ 2 ] [Vargheese, Vibin]Univ Tokyo, Dept Chem Syst Engn, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1138656, Japan
  • [ 3 ] [Ghampson, I. Tyrone]Univ Tokyo, Dept Chem Syst Engn, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1138656, Japan
  • [ 4 ] [Yun, Gwang-Nam]Univ Tokyo, Dept Chem Syst Engn, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1138656, Japan
  • [ 5 ] [Oyama, S. Ted]Univ Tokyo, Dept Chem Syst Engn, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1138656, Japan
  • [ 6 ] [Murakami, Junichi]Natl Inst Adv Ind Sci & Technol, 2D Nanomat Grp, 1-1-1 Higashi, Tsukuba, Ibaraki 3058565, Japan
  • [ 7 ] [Bando, Kyoko K.]Natl Inst Adv Ind Sci & Technol, 2D Nanomat Grp, 1-1-1 Higashi, Tsukuba, Ibaraki 3058565, Japan
  • [ 8 ] [Yun, Gwang-Nam]Virginia Tech, Dept Chem Engn, Blacksburg, VA 24061 USA
  • [ 9 ] [Oyama, S. Ted]Virginia Tech, Dept Chem Engn, Blacksburg, VA 24061 USA
  • [ 10 ] [Yun, Gwang-Nam]Korea Res Inst Chem Technol KRICT, Green Carbon Res Ctr, 141 Gajeong Ro, Daejeon 34114, South Korea
  • [ 11 ] [Kobayashi, Yasukazu]Natl Inst Adv Ind Sci & Technol, Interdisciplinary Res Ctr Catalyt Chem, Cent 5,1-1-1 Higashi, Tsukuba, Ibaraki 3058565, Japan

Reprint 's Address:

  • 大山茂生

    [Yun, Gwang-Nam]Univ Tokyo, Dept Chem Syst Engn, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1138656, Japan;;[Oyama, S. Ted]Univ Tokyo, Dept Chem Syst Engn, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1138656, Japan

Show more details

Related Keywords:

Source :

JOURNAL OF CATALYSIS

ISSN: 0021-9517

Year: 2020

Volume: 389

Page: 352-365

7 . 9 2

JCR@2020

6 . 5 0 0

JCR@2023

ESI Discipline: CHEMISTRY;

ESI HC Threshold:160

JCR Journal Grade:1

CAS Journal Grade:1

Cited Count:

WoS CC Cited Count: 0

SCOPUS Cited Count: 20

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 0

Online/Total:195/10059035
Address:FZU Library(No.2 Xuyuan Road, Fuzhou, Fujian, PRC Post Code:350116) Contact Us:0591-22865326
Copyright:FZU Library Technical Support:Beijing Aegean Software Co., Ltd. 闽ICP备05005463号-1