文献类型：期刊文献

中文题名：Improved oxidation of hydrogen off-gas by hydrophobic surface modification: A multiscale density functional theory study

作者：Cheng Lian[1,2];Cheng Cai[2];Xiangjian Shen[3];Shuangliang Zhao[1];Xinhai Yu[4];Honglai Liu[2]

机构：[1]State Key Laboratory of Chemical Engineering and School of Chemical Engineering, East China University of Science and Technology, Shanghai 200237, China;[2]School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai 220237, China;[3]Research Center of Heterogeneous Catalysis and Engineering Science, School of Chemical Engineering and Energy, Zhengzhou University, Zhengzhou 450001, China;[4]Key Laboratory of Safety Science of Pressurized System (MOE), School of Mechanical Engineering, East China University of Science and Technology, Shanghai 200237, China

年份：2019

卷号：17

期号：3

起止页码：28

中文期刊名：Particuology

外文期刊名：颗粒学报（英文版）

收录：CSTPCD;;Scopus;CSCD:【CSCD2019_2020】；

基金：the National Natural Science Foundation of China(Nos.91434110 and U1707602);the National Natural Science Foundation of China for Innovative Research Groups(No.51621002);the 111 Project of China(No.B08021);the PetroChina Innovation Foundation(No.2017D5007-0204);SZ acknowledges the support of the Fok Ying Tong Education Foundation(No.151069).

语种：英文

中文关键词：Surface;reaction;Hydrophobic;modification;Density;functional;theory;Multiscale

摘要：A catalytic micro-reactor for converting hydrogen off-gas into water was recently developed, through which the conversion efficiency of hydrogen gas was greatly improved by hydrophobic modification of the catalytic substrate. Herein, a hybrid theoretical method is reported that combines density functional theory (DFT) on both the quantum and molecular scales. This method allows the microscopic study of the mechanism by which the surface catalytic reaction can be manipulated. Specifically, quantum DFT calculations are performed to quantify the molecular interaction between the catalytic substrate and reagent or product. Classical DFT investigations are subsequently carried out to determine the local concentrations of reagents near catalytic sites subject to different surface coating conditions. Finally, the reaction efficiency is determined from the local concentrations based on collision theory. This multiscale method provides molecular insight for quantifying the effect of catalytic surface modification on the reaction efficiency. The method reveals that an optimal surface hydrophobic modification can promote the densities of reagents near the substrate, while depleting the produced water. These two factors promote the conversion efficiency. The exclusion of produced water from the catalytic substrate is affected more by the degree of polymer grafting than by the chain length of hydrophobic polymer moieties.