化学
氧化磷酸化
试剂
接触角
金属
傅里叶变换红外光谱
X射线光电子能谱
氧化物
疏水效应
有机化学
多相催化
化学工程
组合化学
无机化学
氧气
红外光谱学
嫁接
催化作用
疏水
过渡金属
高分子化学
疏水二氧化硅
氧化还原
作者
Na Zhao,Xuanjiao Zhao,X. R. Zhou,Tingzhen Zhang,Chuxin Huang,Shanshan Liu,Yuchao Li,Cuncun Zuo,Rui Xu,Haofei Huang,Yansong Zhao
标识
DOI:10.1021/acs.iecr.5c03337
摘要
Hydrophobic catalysts play a crucial role in promoting oxidative esterification. In such reactions, water, formed as a byproduct, can occupy active sites, thereby reducing catalytic activity. A series of hydrophobic catalysts (Au@M–Si-y, M = ZnO, Ce2O, or Al2O3) was designed for the oxidative esterification of methacrolein. These catalysts utilize metal oxides as supports and integrate trimethylchlorosilane as a hydrophobic group to produce hydrophobic metal oxide supports. The active component, Au, was immobilized on the hydrophobic supports using the deposition–precipitation technique, and then the Au-based hydrophobic catalyst was synthesized. Scanning electron microscopy and Fourier transform infrared spectroscopy analyses confirmed the grafting of Au and hydrophobic groups onto the metal oxide surface. The as-synthesized hydrophobic catalyst exhibited a water droplet contact angle of 71.6°, higher than that of the hydrophobic-group-free Au-based metal oxide catalyst. X-ray photoelectron spectroscopy revealed that the gold was mainly in a metallic state, facilitating oxygen activation and thus accelerating the reaction. For Au@ZnO–Si-y, the catalytic activity first increased and then decreased with increasing TMCS loading, indicating that the moderate degree of hydrophobicity of the catalyst promotes the reaction. Based on reaction kinetics, the activation energy was 29.42 kJ mol–1.
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