Compensation in the isopropyl alcohol dehydration over sol-gel Al2O3-TiO2 oxides: Effect of calcining temperature

被引:12
|
作者
Escobar, J. [1 ]
Reyes, J. A. De Los [2 ]
Viveros, T. [2 ]
Valle-Orta, M. [3 ]
Barrera, M. C. [4 ]
机构
[1] Inst Mexicano Petr, Mexico City 07730, DF, Mexico
[2] Univ Autonoma Metropolitana Iztapalapa, Area Ing Quim, Mexico City 09340, DF, Mexico
[3] Lab CIQA PEMEX, Ctr Invest Quim Aplicada, Mexico City 07730, DF, Mexico
[4] Univ Veracruzana, Fac Ciencias Quim, Coatzacoalcos 96538, Veracruz, Mexico
关键词
Alumina-titania mixed oxides; Isopropanol dehydration; Compensation effect; Constable plot; Isokinetic temperature; PRECURSOR; CATALYSTS; KINETICS; SITES;
D O I
10.1016/j.fuel.2014.09.016
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Compensation effects were found in isopropanol dehydration over alumina (A), titania (T) and corresponding mixed oxides (Al/Ti = 2 and 25 mol ratio, AT2 and AT25, respectively) synthesized by low-temperature sol-gel. Prepared materials (calcined in the 573-1173 K) range were characterized by several techniques (N-2 physisorption, XRD, thermal analysis and SEM). In general, Al2O3 had the highest reaction rate (at 473 K) in propylene formation meanwhile both mixed oxides had much lower activity. TiO2 had minimal dehydrating activity that, nevertheless, was the highest intrinsic one (in areal basis). Constable plots were obtained for materials annealed at various temperatures, but for titania series. A clear isokinetic temperature (T-theta) was observed for alumina series whereas for AT25 materials, a T-theta pole was registered but for the sample calcined at the most severe condition. Meanwhile, two T-theta poles were identified for AT2 solids, the first one corresponding to materials calcined at moderate temperature whereas the other set apart solids annealed under severe conditions. As expected, no isokinetic temperature was observed in Arrhenius plots corresponding to alcohol dehydration over TiO2 materials. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:109 / 117
页数:9
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