Zirconia-supported 12-tungstophosphoric acid as a solid catalyst for the synthesis of linear alkyl benzenes

被引:95
作者
Devassy, BM
Lefebvre, F
Halligudi, SB [1 ]
机构
[1] Natl Chem Lab, Inorgan Chem & Catalysis Div, Pune 411008, Maharashtra, India
[2] CNRS, Lab Chem Organomet Surface, CPE, Villeurbanne, France
关键词
zirconia; 12-tungstophosphoric acid; solvent effect; linear alkyl benzene;
D O I
10.1016/j.jcat.2004.09.024
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The liquid-phase alkylation of benzene with 1-octene and 1-dodecene was investigated with zirconia-supported 12-tungstophosphoric acid (TPA) as catalysts. We prepared the catalysts, with different TPA loading (5-20 wt% calcined at 750 degrees C) and calcination temperatures (15 wt% calcined from 650 to 850 degrees C), by suspending hydrous zirconia in a methanol solution of TPA, followed by drying and calcination. These catalysts were characterized by X-ray diffraction, DTG-DTA, FTIR pyridine adsorption, NH3-TPD, and P-31, MAS NMR spectroscopy measurements. The catalyst with optimum TPA loading (15%) and calcination temperature (750 degrees C) was prepared in different solvents and characterized by P-31 MAS NMR spectroscopy. The XRD results indicate that TPA stabilizes the tetragonal phase of zirconia. The catalysts show both Bronsted and Lewis acidity, and 15% TPA on zirconia calcined at 750 degrees C shows the highest acidity. P-31 MAS NMR spectra show two types of phosphorous species: one is the Keggin unit and the other is the decomposition product of TPA. The relative amount of each depends on TPA loading, calcination temperature, and the solvent used for the catalyst preparation. Under reaction conditions of 84 degrees C and a benzene/1-olefin molar ratio of 10 (time 1 h), the most active catalyst, 15% TPA, calcined at 750 degrees C, gave more than 98% olefin conversion with selectivity for 2-phenyl octane (53.5%) and 2-phenyl dodecane (47%). (c) 2004 Elsevier Inc. All rights reserved.
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页码:1 / 10
页数:10
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共 40 条
  • [1] Present general status of understanding of heteropoly electrolytes and a tracing of some major highlights in the history of their elucidation
    Baker, LCW
    Glick, DC
    [J]. CHEMICAL REVIEWS, 1998, 98 (01) : 3 - 49
  • [2] Solid acid catalysts based on supported tungsten oxides
    Barton, DG
    Soled, SL
    Iglesia, E
    [J]. TOPICS IN CATALYSIS, 1998, 6 (1-4) : 87 - 99
  • [3] An investigation into the preparation of high surface area zirconia
    Chuah, GK
    [J]. CATALYSIS TODAY, 1999, 49 (1-3) : 131 - 139
  • [4] A new solid acid-based route to linear alkylbenzenes
    Clark, JH
    Monks, GL
    Nightingale, DJ
    Price, PM
    White, JF
    [J]. JOURNAL OF CATALYSIS, 2000, 193 (02) : 348 - 350
  • [5] Lewis acids:: From conventional homogeneous to green homogeneous and heterogeneous catalysis
    Corma, A
    García, H
    [J]. CHEMICAL REVIEWS, 2003, 103 (11) : 4307 - 4365
  • [6] INORGANIC SOLID ACIDS AND THEIR USE IN ACID-CATALYZED HYDROCARBON REACTIONS
    CORMA, A
    [J]. CHEMICAL REVIEWS, 1995, 95 (03) : 559 - 614
  • [7] Thermal behavior of 12-molybdophosphoric acid supported on zirconium-loaded silica
    Damyanova, S
    Gomez, LM
    Bañares, MA
    Fierro, JLG
    [J]. CHEMISTRY OF MATERIALS, 2000, 12 (02) : 501 - 510
  • [8] Infrared study of pyridine adsorbed on unpromoted and promoted sulfated zirconia
    Davis, BH
    Keogh, RA
    Alerasool, S
    Zalewski, DJ
    Day, DE
    Doolin, PK
    [J]. JOURNAL OF CATALYSIS, 1999, 183 (01) : 45 - 52
  • [9] LINEAR ALKYLBENZENE
    DEALMEIDA, JLG
    DEFAUX, M
    TAARIT, YB
    NACCACHE, C
    [J]. JOURNAL OF THE AMERICAN OIL CHEMISTS SOCIETY, 1994, 71 (07) : 675 - 694
  • [10] Immobilised ionic liquids as Lewis acid catalysts for the alkylation of aromatic compounds with dodecene
    DeCastro, C
    Sauvage, E
    Valkenberg, MH
    Hölderich, WF
    [J]. JOURNAL OF CATALYSIS, 2000, 196 (01) : 86 - 94