A practical grinding-assisted dry synthesis of nanocrystalline NiMoO4 polymorphs for oxidative dehydrogenation of propane

被引:29
作者
Chen, Miao [1 ,2 ]
Wu, Jia-Ling [1 ]
Liu, Yong-Mei [1 ]
Cao, Yong [1 ]
Guo, Li [2 ]
He, He-Yong [1 ]
Fan, Kang-Nian [1 ]
机构
[1] Fudan Univ, Dept Chem, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R China
[2] Zhejiang Chem Ind Res Inst, Hangzhou 310023, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
NiMoO4; Nanocrystalline; Grinding; Propane; Oxidative dehydrogenation; NICKEL MOLYBDATE CATALYSTS; SELECTIVE OXIDATION; C-4; HYDROCARBONS; MALEIC-ANHYDRIDE; LOW-TEMPERATURE; EXCESS MOO3; ACTIVATION; OXIDES; CONVERSION; KINETICS;
D O I
10.1016/j.jssc.2011.10.024
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A practical two-stage reactive grinding-assisted pathway waste-free and cost-effective for the synthesis of NiMoO4 has been successfully developed. It was demonstrated that proper design in synthetic strategy for grinding plays a crucial role in determining the ultimate polymorph of NiMoO4. Specifically, direct grinding (DG) of MoO3 and NiO rendered alpha-NiMoO4 after annealing, whereas sequential grinding (SG) of the two independently pre-ground oxides followed by annealing generated beta-NiMoO4 solid solution. Characterizations in terms of Raman and X-ray diffraction suggest the creation of beta-NiMoO4 precursor in the latter alternative is the key aspect for the formation of beta-NiMoO4. The DG-derived alpha-NiMoO4 tested by oxidative dehydrogenation of propane exhibited superior activity in contrast to its analog synthesized via conventional coprecipitation. It is suggested that the favorable chemical composition facilely obtained via grinding in contrast to that by coprecipitation was essential for achieving a more selective production of propylene. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:3357 / 3363
页数:7
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