Catalytic activity of tungsten-doped titanium dioxide-supported platinum catalysts in the sequential hydrogenolysis of glycerol: effect of support calcination temperature

IF 1.7 4区 化学 Q4 CHEMISTRY, PHYSICAL
Chao Yu, Changlin Chen
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引用次数: 0

Abstract

Two Pt-WOx/TiO2 catalysts with the same content of Pt and WOx were prepared by impregnation-calcination method and treated with WOx/TiO2 supports at different temperatures, and their catalytic performance in the preparation of 1,3-propanediol (1,3-PDO) by selective hydrogenolysis of glycerol was studied. The catalysts were characterized by N2 adsorption–desorption, CO chemisorption, Thermogravimetric analysis, X-ray diffraction, High-resolution transmission electron microscopy, NH3-temperature-programmed desorption, H2-temperature-programmed reduction, Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy. The results showed that the Pt-WOx/TiO2 catalyst with high temperature treatment had the highest activity, with a glycerol conversion rate of 71.4% and a selectivity of 36.4% for 1,3-PDO at 160 °C and 4 MPa, while the catalyst treated with low temperature was only 5.2% and 10.6%. In this regard, increasing the treatment temperature of the catalyst did not change the crystalline phase structure of TiO2, but changed the diameter structure of the catalyst pore, improved the crystallinity of the catalyst support and the dispersion of Pt particles on the surface, reduced the amount of acid in the catalyst, and enhanced the interaction between Pt, WOx and TiO2 in the catalyst.

掺钨二氧化钛负载铂催化剂在甘油序贯氢解中的催化活性:负载煅烧温度的影响
采用浸渍-煅烧法制备了Pt和WOx含量相同的两种Pt-WOx/TiO2催化剂,并用WOx/TiO2载体在不同温度下处理,研究了它们在甘油选择性氢解法制备1,3-丙二醇(1,3- pdo)中的催化性能。采用N2吸附-脱附、CO化学吸附、热重分析、x射线衍射、高分辨率透射电镜、nh3程序升温脱附、h2程序升温还原、傅里叶变换红外光谱和x射线光电子能谱对催化剂进行了表征。结果表明,高温处理的Pt-WOx/TiO2催化剂活性最高,在160℃和4 MPa条件下甘油转化率为71.4%,对1,3- pdo的选择性为36.4%,而低温处理的催化剂仅为5.2%和10.6%。由此可见,提高催化剂的处理温度并没有改变TiO2的晶相结构,但改变了催化剂孔的直径结构,提高了催化剂载体的结晶度和Pt颗粒在表面的分散性,减少了催化剂中的酸量,增强了催化剂中Pt、WOx和TiO2的相互作用。
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来源期刊
CiteScore
3.30
自引率
5.60%
发文量
201
审稿时长
2.8 months
期刊介绍: Reaction Kinetics, Mechanisms and Catalysis is a medium for original contributions in the following fields: -kinetics of homogeneous reactions in gas, liquid and solid phase; -Homogeneous catalysis; -Heterogeneous catalysis; -Adsorption in heterogeneous catalysis; -Transport processes related to reaction kinetics and catalysis; -Preparation and study of catalysts; -Reactors and apparatus. Reaction Kinetics, Mechanisms and Catalysis was formerly published under the title Reaction Kinetics and Catalysis Letters.
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