Transient acrolein selectivity and carbon deposition study of glycerol dehydration over WO3/TiO2 catalyst

被引:40
作者
Dalil, Marjan [1 ]
Carnevali, Davide [1 ]
Dubois, Jean-Luc [2 ]
Patience, Gregory S. [1 ]
机构
[1] Polytech Montreal, Dept Chem Engn, Montreal, PQ H3C 3A7, Canada
[2] ARKEMA, F-69493 Pierre Benite, France
基金
加拿大自然科学与工程研究理事会;
关键词
Glycerol; Dehydration; Acrolein; WO3-TiO2; Kinetics; Fluidized-bed; GAS-PHASE DEHYDRATION; ACRYLIC-ACID; 1,2-PROPANEDIOL; HYDROGENOLYSIS; CONVERSION; OXIDATION; KINETICS;
D O I
10.1016/j.cej.2015.02.058
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Acrolein is one of the highest valued commodity chemicals for which glycerol is an attractive feedstock. Glycerol is derived from transesterification of vegetable oils and animal fats. WO3/TiO2 catalyst dehydrated glycerol to acrolein at a selectivity exceeding 73% after 6 h time-on-stream. However, after 1 h, the acrolein selectivity was only 55%. All the glycerol reacted at reaction temperature (280 degrees C) and the by-products were predominantly propanal, acetaldehyde, formic and acetic acids. The weight gain of carbon on the catalyst increased with time and after one hour, the mass fraction of carbon was 2.2%; after an additional five hours, it doubled. A first order kinetic model characterizes the rate at which oxygen reacts the carbon on the catalyst with an activation energy of 100 kJ mol(-1) (R-2 >0.997). Partial oxidation of coke, as a new strategy for catalyst regeneration, enhanced the selectivity toward acrolein from 10% to 25% in the first 15 min of glycerol injection. Glycerol conversion to coke was reduced from 34% to 6%. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:557 / 563
页数:7
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