The selective oxidation of methanol to formaldehyde using novel iron molybdate catalysts prepared by supercritical antisolvent precipitation

被引:0
作者
Pitchers, Jack R. [1 ]
Carter, James [1 ]
Genc, Aziz [1 ]
Slater, Thomas J. A. [1 ]
Morgan, David J. [1 ]
Oakley, Alice [2 ]
Vandegehuchte, Bart D. [3 ]
Taylor, Stuart H. [1 ]
Hutchings, Graham J. [1 ]
机构
[1] Cardiff Univ, Cardiff Catalysis Inst, Sch Chem, Translat Res Hub, Maindy Rd, Cardiff, Wales
[2] Southampton Univ, Sch Chem, Highfield Campus, Southampton, Hants, England
[3] TotalEnergies OneTech Belgium, Zone Ind C, B-7181 Feluy, Belgium
关键词
OXIDE PARTICLES; SURFACE; BEHAVIOR; CO;
D O I
10.1039/d5cy00211g
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
Iron molybdate catalysts have been extensively explored for the oxidation of methanol to formaldehyde. However, low surface area catalysts are typically formed, and iron-rich phases still exist from common preparation methods, leading to lower selectivity. The use of supercritical antisolvent precipitation to form novel precursors led to catalysts with improved productivity compared to alternative precipitation techniques. Using isoconversion studies, new structure-performance relationships have been uncovered. The novel iron molybdate catalysts provided an improved formaldehyde production of 42.5 mmolCH2O gcat-1 h-1 for the best performing catalyst, whilst specific productivity was used as a descriptor to probe intrinsic properties of the catalysts. Improved performance was achieved by increased agglomerate size and by phase purity, both controlled by the precursor structure. Both properties improve the supply of oxygen to the amorphous MoOx surface phase from the reducible crystalline phase.
引用
收藏
页码:3195 / 3203
页数:9
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