Selective Oxidation and Oxidative Dehydrogenation of Isobutane over Hydrothermally Synthesized Mo-V-O Mixed Oxide Catalysts

被引:10
作者
Guan, Jingqi [1 ]
Xu, Haiyan [1 ]
Song, Ke [1 ]
Liu, Bo [1 ]
Shang, Fanpeng [1 ]
Yu, Xiaofang [1 ]
Kan, Qiubin [1 ]
机构
[1] Jilin Univ, Coll Chem, Changchun 130023, Peoples R China
基金
中国国家自然科学基金;
关键词
Isobutane; Isobutene; Selective oxidation; Methacrolein; Mo-V-O mixed oxide catalysts;
D O I
10.1007/s10562-008-9613-3
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 series of Mo-V-O catalysts were prepared by calcining the orthorhombic (M1) Mo-V-O phase containing precursors under different conditions (T = 500 or 600 C in atmosphere of N-2 or air) and tested for the oxidation of isobutane and isobutene. Characterization results (BET, XRD, XPS, FTIR, and TPR) showed that their structure and properties depend on the composition of the calcined samples and the calcined conditions. Catalytic tests showed that relatively high isobutane conversion and desired product selectivity can be achieved over MoV0.3-500-N and MoV0.3-600-A catalysts. It is also found that both orthorhombic M1 phase and (V0.07M0.93)(5)O-14 phase are active and selective for the selective oxidation of isobutane to methacrolein, whereas higher selectivity toward methacrolein (40.4%) can be achieved over the former phase at a moderate isobutane conversion (6.4%). Moreover, (Mo0.3V0.7)(2)O-5 phase may be propitious to complete oxidation for the selective oxidation of isobutane. On the other hand, the presence of V affects the activity and selectivity, and a low surface V4+ concentration prefers selective oxidation products. In addition, specific surface areas of the catalysts appear to be little important in determining the catalytic activation.
引用
收藏
页码:293 / 300
页数:8
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