Understanding the surface and structural characteristics of tungsten oxide supported on tin oxide catalysts for the conversion of glycerol

被引:13
|
作者
Srinivas, M. [1 ]
Raveendra, G. [1 ]
Parameswaram, G. [1 ]
Prasad, P. S. Sai [1 ]
Loridant, S. [2 ]
Lingaiah, N. [1 ]
机构
[1] Indian Inst Chem Technol, CSIR, I & PC Div, Catalysis Lab, Hyderabad 500007, Andhra Pradesh, India
[2] Univ Lyon 1, CNRS, Inst Recherchessur Catalyse & Environm Lyon, IRCELYON,UMR 5256, F-69626 Villeurbanne, France
关键词
Tungsten oxide; tin oxide; etherification; glycerol; tert-butanol; glycerol ethers; DIMETHYL CARBONATE; ACID CATALYSTS; SOLID ACIDS; ETHERIFICATION; UREA; TRANSESTERIFICATION; EXCHANGE; SNO2; ESTERIFICATION; TRANSFORMATION;
D O I
10.1007/s12039-015-0848-4
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Catalysts with varying WO3 content on SnO2 were prepared and characterized by X-ray diffraction, in situ Raman spectroscopy, X-ray photoelectron spectroscopy and temperature programmed desorption of NH3. In situ Raman analysis reveals the presence isolated monomers and polymeric species of WO3. These catalysts were evaluated for the conversion of glycerol into value added chemicals. Etherification of glycerol with tertiary butanol and preparation of glycerol carbonate from glycerol and urea are studied over these catalysts. The catalytic activity results suggest that the glycerol conversion and selectivity depends on the morphology of WO3 which in turn is related to its content in the catalyst. The catalysts with 5 wt.% of WO3 on SnO2 resulted in high dispersion with larger number of strong acidic sites. The selectivity in the glycerol etherification is related to the nature of the catalyst and reaction time. These catalysts also exhibited high activity for synthesis of glycerol carbonate. The effect of various reaction parameters was studied to optimize the reaction conditions. The catalysts also exhibited consistent activity upon reuse.
引用
收藏
页码:897 / 908
页数:12
相关论文
共 50 条
  • [41] Electrochemical oxidation of CO over tin oxide supported platinum catalysts
    Matsui, T
    Fujiwara, K
    Okanishi, T
    Kikuchi, R
    Takeguchi, T
    Eguchi, K
    JOURNAL OF POWER SOURCES, 2006, 155 (02) : 152 - 156
  • [42] Molecular/electronic structure-surface acidity relationships of model-supported tungsten oxide catalysts
    Kim, Taejin
    Burrows, Andrew
    Kiely, Christopher J.
    Wachs, Israel E.
    JOURNAL OF CATALYSIS, 2007, 246 (02) : 370 - 381
  • [43] EFFECT OF OXIDE PROMOTERS ON THE SURFACE CHARACTERISTICS OF CARBON-SUPPORTED CO AND RU CATALYSTS
    RODRIGUEZRAMOS, I
    GUERRERORUIZ, A
    FIERRO, JLG
    APPLIED SURFACE SCIENCE, 1989, 40 (03) : 239 - 247
  • [44] Cellulose conversion to ethylene glycol by tungsten oxide-based catalysts
    Wiesfeld, Jan J.
    Persolja, Peter
    Rollier, Floriane A.
    Elemans-Mehring, Adelheid M.
    Hensen, Emiel J. M.
    MOLECULAR CATALYSIS, 2019, 473 : 92 - 101
  • [45] Preparation of supported vanadium oxide catalysts: The role of surface molecular chemistry on oxide surface structure
    Wegener, Staci L.
    Kim, Hacksung
    Marks, Tobin J.
    Stair, Peter C.
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2011, 241
  • [46] TIN - ANTIMONY OXIDE CATALYSTS
    BERRY, FJ
    ADVANCES IN CATALYSIS, 1981, 30 : 97 - 131
  • [47] Raman and IR studies of surface metal oxide species on oxide supports: Supported metal oxide catalysts
    Wachs, IE
    CATALYSIS TODAY, 1996, 27 (3-4) : 437 - 455
  • [48] Raman and IR studies of surface metal oxide species on oxide supports: Supported metal oxide catalysts
    Zettlemoyer Ctr. for Surface Studies, Department of Chemical Engineering, Lehigh University, Bethlehem, PA 18015, United States
    Catal Today, 3-4 SPEC. ISS. (437-455):
  • [49] Structural studies of supported tin catalysts
    Noel Nava
    Tomás Viveros
    Hyperfine Interactions, 1999, 122 : 147 - 153
  • [50] Structural studies of supported tin catalysts
    Inst. Mexicano del Petróleo, Gerencia de Catalizadores, Eje Ctrl. Lazaro Cardenas 152, México D.F. 07730, Mexico
    不详
    Hyperfine Interact., 1-2 (147-153):