催化作用
布朗斯特德-洛瑞酸碱理论
离子液体
石墨烯
环加成
氧化物
化学
环氧丙烷
傅里叶变换红外光谱
热重分析
碳酸丙烯酯
X射线光电子能谱
协同催化
无机化学
有机化学
材料科学
化学工程
纳米技术
物理化学
环氧乙烷
聚合物
共聚物
电化学
电极
工程类
作者
Jie Zhu,Shaoqing Wang,Yaokun Gu,Bing Xue,Yongxin Li
标识
DOI:10.1016/j.matchemphys.2018.01.031
摘要
In this work, both hydroxyl and epoxy groups on graphene oxide (GO) were simultaneously employed to immobilize ionic liquids (ILs) via a one-step Bronsted acid catalysis. The resulting materials, consisting of ILs immobilized on GO, were characterized by atomic force microscopy, Fourier transform infrared spectroscopy, thermogravimetry and X-ray photoelectron spectroscopy. The results indicate that the ILs were immobilized on the GO through both the ring opening of epoxy groups and the silylanization of hydroxyl groups in a single step. The amount of IL per unit mass of GO was greatly enhanced by Bronsted acid catalysis compared to the amount deposited without acid catalysis. These materials were applied to the cycloaddition of CO2 with propylene oxide to form propylene carbonate, and exhibited enhanced catalytic activity. The catalyst prepared using a H+ concentration of 80 mmol/L during the Bronsted acid catalysis was approximately 26% more active during the reaction relative to a control prepared without acid catalysis.
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