烷基化
立方氧化锆
催化作用
钒
甲醇
程序升温还原
氧化钒
无机化学
苯酚
化学
解吸
氧化物
核化学
材料科学
有机化学
吸附
陶瓷
作者
Komandur V. R. Chary,K. Ramesh,Guggilla Vidyasagar,Vidya S. Rao
出处
期刊:Journal of Molecular Catalysis A-chemical
[Elsevier BV]
日期:2003-05-01
卷期号:198 (1-2): 195-204
被引量:31
标识
DOI:10.1016/s1381-1169(02)00691-x
摘要
A series of vanadium oxide supported on zirconia catalysts with varying vanadium oxide content (2.5–12.5 wt.%) were prepared by wet impregnation method. The catalysts were characterised by X-ray diffraction (XRD), temperature-programmed reduction (TPR) of hydrogen, temperature-programmed desorption (TPD) of NH3 and specific surface area measurements. X-ray diffraction patterns indicate the presence of crystalline V2O5 phase from 7.5 wt.% of V2O5 on zirconia. TPR patterns reveal the presence of V3+ species on zirconia. Ammonia TPD results suggest that acidity of the catalysts increased with increase in V2O5 loading up to 7.5 wt.% and decreased with further increase in V2O5 loading. The catalytic properties were evaluated for the vapour-phase alkylation of phenol with methanol. During alkylation of phenol with methanol exclusively C-alkylated (alkylation proceeds through ring) products were formed. The selectivity towards 2,6-xylenol was high when compared to o-cresol. The activity of the catalysts was found to increase with V2O5 loading up to 7.5 wt.% of V2O5 and decreased with increase in further vanadia content.
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