An iron molybdate catalyst for methanol to formaldehyde conversion prepared by a hydrothermal method and its characterization

被引:67
作者
Beale, Andrew M. [1 ]
Jacques, Simon D. M. [2 ]
Sacaliuc-Parvalescu, Elena [1 ]
O'Brien, Matthew G. [1 ]
Barnes, Paul [2 ]
Weckhuysen, Bert M. [1 ]
机构
[1] Univ Utrecht, Debye Inst NanoMat Sci, NL-3584 CA Utrecht, Netherlands
[2] UCL, Dept Chem, London WC1H 0AJ, England
基金
英国工程与自然科学研究理事会;
关键词
Iron molybdate; Hydrothermal; Methanol-to-formaldehyde; RAY-ABSORPTION-SPECTROSCOPY; IN-SITU; SELECTIVE OXIDATION; ELECTRON-MICROSCOPY; BISMUTH MOLYBDATES; RAMAN-SPECTROSCOPY; CRYSTAL-STRUCTURE; MOLYBDENUM OXIDE; METAL OXIDES; PHASE;
D O I
10.1016/j.apcata.2009.05.008
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
A one-step, low-temperature hydrothermal method has been successfully employed to prepare iron molybdate catalysts with Mo:Fe ratios ranging from 1.5:1 to 3.0:1. The resulting materials were characterized using a number of techniques including: XRD, Raman, N-2 adsorption, SEM/EDX, DTA, EDXRD and combined XRD/XAS. The catalytic oxidative dehydrogenation of methanol to formaldehyde has been used as a test reaction. For Mo:Fe similar to 1.5, phase-pure Fe-2(MoO4)(3) resulted from syntheses performed at temperatures as low as 100 degrees C in under 4 h. For samples with a Mo:Fe similar to 3 detailed analysis of XRD, Raman and EXAFS data revealed the formation of a high surface area possessing, mixed phase material consisting of a poorly crystalline Mo5O14 and an amorphous Fe-2(MoO4)(3) type precursor. Both phases proved to be thermally unstable above a calcination temperature of 300 degrees C, going on to form high surface area mixed Fe-2(MoO4)(3)/MoO3. Continued heating of this mixed oxide material resulted in sintering and to a decrease in the surface area. When both mildly (200 degrees C) and then more severely calcined (300 degrees C) this mixed phase sample showed a higher selectivity for formaldehyde production than a conventionally prepared (via co-precipitation) iron molybdate catalyst. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:143 / 152
页数:10
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