Real-time in situ ATR-FTIR analysis of the liquid phase hydrogenation of γ-butyrolactone over Cu-ZnO catalysts:: A mechanistic study by varying lactone ring size

被引:71
作者
Hamminga, GM [1 ]
Mul, G [1 ]
Moulijn, JA [1 ]
机构
[1] Delft Univ Technol, Fac Sci Appl, DelftChemTech, NL-2628 BL Delft, Netherlands
关键词
chemical analysis; heterogeneous catalysis; hydrogenation of lactones; kinetics; multiphase reactions; real-time in situ ATR-FTIR analysis; selectivity;
D O I
10.1016/j.ces.2004.07.087
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Real-time in situ attenuated total reflection (ATR) FTIR spectroscopy is a powerful tool for both kinetic and mechanistic studies of heterogeneous catalytic liquid phase reactions at high temperature and pressure. This is illustrated by the liquid phase hydrogenation of T-butyrolactone (five ring) to 1,4-butanediol over a copper zinc oxide catalyst at 453 K and a total hydrogen pressure of 5.0 MPa. The concentration profiles of the hydrogenation reaction obtained by this real-time analysis technique are in excellent agreement with conventional off-line GC analysis. Complementary results were found for the hydrogenation of delta-valerolactone (six ring) to 1,5-pentanediol. When investigating g-caprolactone (seven ring), a severe change in reaction selectivity was observed. This was explained by a significant change in reaction mechanism. However, by conduction several additional experiments a clear mechanistic picture could be created for the three lactone hydrogenation reactions. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5479 / 5485
页数:7
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