Adsorptive desulfurization of thiophene over Ti0.9Ce0.1O2 mixed oxide: A mechanistic study on the basis of XPS, in-situ FT-IR and TPD characterizations

被引:7
|
作者
Watanabe, Shingo [1 ,2 ]
Ma, Xiaoliang [3 ]
Song, Chunshan
机构
[1] Penn State Univ, Clean Fuels & Catalysis Program, EMS Energy Inst, 209 Acad Project Bldg, University Pk, PA 16802 USA
[2] Nanoram Labs, Boston, MA 02210 USA
[3] Kuwait Inst Sci Res, Kuwait, Kuwait
基金
美国国家科学基金会;
关键词
Adsorptive desulfurization; TiO2-CeO2; oxide; Thiophene; Adsorption mechanism; Dissociative adsorption; DEEP DESULFURIZATION; SELECTIVE ADSORPTION; JET FUEL; OXIDATIVE DESULFURIZATION; TIO2(110) SURFACES; ADSORBED THIOPHENE; SULFUR-COMPOUNDS; IONIC LIQUIDS; CERIUM OXIDE; DIESEL FUEL;
D O I
10.1016/j.cattod.2020.07.066
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The adsorption of thiophenic compounds over Ti0.9Ce0.1O2, an oxidatively regenerable sulfur adsorbent, was studied by XPS, DRIFT, and TPD-MS. Effect of the oxidative pretreatment on thiophene adsorption over Ti0.9Ce0.1O2 adsorbent, the adsorption site for thiophenic compound, and the role of surface Ce and Ti cations in the adsorptive desulfurization (ADS) were investigated. The results suggest that the surface oxygen plays an essential role in ADS and is a major active site for chemical adsorption of the thiophenic compounds. The surface Ce and Ti were further oxidized by the surface oxygen in the oxidative pretreatment, and then reduced during the adsorption of thiophenic compounds. This phenomenon is attributed to an electron transfer from the adsorbates to the surface Ce and Ti. It appears that the role of the surface Ce and Ti can accept electrons from adsorbate, and also contributes to producing the active oxygen to oxidize the sulfur atom of thiophenic compounds. An oxidative pretreatment, including oxidative regeneration, activates the surface oxygen to forms active oxygen species and oxidizes the surface Ce and Ti. Based on the results obtained, a possible mechanism was proposed for the chemical adsorption, dissociation and surface reaction of thiophene on Ti0.9Ce0.1O2 mixed metal oxide adsorbent.
引用
收藏
页码:276 / 286
页数:11
相关论文
共 8 条
  • [1] Air-Promoted Adsorptive Desulfurization over Ti0.9Ce0.1O2 Mixed Oxides from Diesel Fuel under Ambient Conditions
    Xiao, Jing
    Sitamraju, Siddarth
    Chen, Yongsheng
    Janik, Michael
    Song, Chunshan
    CHEMCATCHEM, 2013, 5 (12) : 3582 - 3586
  • [2] In-Situ FT-IR Study on Methane Combustion over Pd/NiAl2O4 Catalyst
    Liu Ying
    Wang Sheng
    Gao Diannan
    Pan Qiushi
    Wang Shudong
    CHINESE JOURNAL OF CATALYSIS, 2012, 33 (09) : 1552 - 1557
  • [3] In situ XAFS study of highly reducible mixed oxide catalysts Ce0.9Pd0.1O2-δ and Ce0.7Yb0.2Pd0.1O2-δ
    Piskorska-Hommel E.
    Kowalska D.A.
    Kraszkiewicz P.
    Kurnatowska M.
    Journal of Alloys and Compounds, 2020, 831
  • [4] In situ FT-IR and TPD-MS study of carbon monoxide oxidation over a CeO2/CO3O4 catalyst
    Tang, Chih-Wei
    Hsu, Li-Chia
    Yu, Shen-Wei
    Wang, Chen-Bin
    Chien, Shu-Hua
    VIBRATIONAL SPECTROSCOPY, 2013, 65 : 110 - 115
  • [5] In situ XAFS study of highly reducible mixed oxide catalysts Ce 0.9 Pd 0.1 O 2-5 and Ce 0.7 Yb 0.2 Pd 0.1 O 2-5
    Piskorska-Hommel, Edyta
    Kowalska, Dorota A.
    Kraszkiewicz, Piotr
    Kurnatowska, Michalina
    JOURNAL OF ALLOYS AND COMPOUNDS, 2020, 831
  • [6] In-Situ FT-IR Study on the Mechanism of CO2 Reduction with Water over Metal (Ag or Au) Loaded Ga2O3 Photocatalysts
    Yamamoto, Muneaki
    Yoshida, Tomoko
    Yamamoto, Naoto
    Yoshida, Hisao
    Yagi, Shinya
    E-JOURNAL OF SURFACE SCIENCE AND NANOTECHNOLOGY, 2014, 12 : 299 - 303
  • [7] In-situ FT-IR study on CO2 hydrogenation over Cu catalysts supported on SiO2, Al2O3, and TiO2
    Bando, KK
    Sayama, K
    Kusama, H
    Okabe, K
    Arakawa, H
    APPLIED CATALYSIS A-GENERAL, 1997, 165 (1-2) : 391 - 409
  • [8] In-situ FT-IR spectroscopy and kinetic study of methanol synthesis from CO/H-2 over ZnAl2O4 and Cu-ZnAl2O4 catalysts
    LePeltier, F
    Chaumette, P
    Saussey, J
    Bettahar, MM
    Lavalley, JC
    JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 1997, 122 (2-3) : 131 - 139