Crole David A, Freakley Simon J, Edwards Jennifer K, Hutchings Graham J
Cardiff Catalysis Institute and School of Chemistry , Main Building, Park Place, Cardiff CF10 3AT, UK.
Proc Math Phys Eng Sci. 2016 Jun;472(2190):20160156. doi: 10.1098/rspa.2016.0156.
The direct synthesis of hydrogen peroxide (HO) from hydrogen and oxygen has been studied using an Au-Pd/TiO catalyst. The aim of this study is to understand the balance of synthesis and sequential degradation reactions using an aqueous, stabilizer-free solvent at ambient temperature. The effects of the reaction conditions on the productivity of HO formation and the undesirable hydrogenation and decomposition reactions are investigated. Reaction temperature, solvent composition and reaction time have been studied and indicate that when using water as the solvent the HO decomposition reaction is the predominant degradation pathway, which provides new challenges for catalyst design, which has previously focused on minimizing the subsequent hydrogenation reaction. This is of importance for the application of this catalytic approach for water purification.
已使用金-钯/二氧化钛催化剂研究了由氢气和氧气直接合成过氧化氢(HO)的过程。本研究的目的是在环境温度下,使用无稳定剂的水性溶剂来理解合成反应与后续降解反应之间的平衡。研究了反应条件对HO生成产率以及不良氢化和分解反应的影响。对反应温度、溶剂组成和反应时间进行了研究,结果表明,当使用水作为溶剂时,HO分解反应是主要的降解途径,这给催化剂设计带来了新的挑战,此前催化剂设计主要关注将后续氢化反应降至最低。这对于这种催化方法在水净化中的应用至关重要。