Effect of initial nickel particle size on stability of nickel catalysts for aqueous phase reforming

作     者：Tomas van Haasterecht Marten Swart Krijn P.de Jong Johannes Hendrik Bitter 

作者机构：Inorganic Chemistry and Catalysis Utrecht University 3508 TB Utrecht The Netherlands Biobased Chemistry and Technology Wageningen University 6708 WG Wageningen The Netherlands 

出 版 物：《Journal of Energy Chemistry》 (能源化学（英文版）)

年 卷 期：2016年第25卷第2期

页      面：287-294页

核心收录：

学科分类：081705[工学-工业催化] 08[工学] 0817[工学-化学工程与技术] 

基　　金：the support of the Smart Mix Program of The Netherlands Ministry of Economic Affairs  Agriculture and Innovation and The Netherlands Ministry of Education  Culture and Science (Grant no. 053.70.011) 

主　　题：Aqueous phase reforming Particle growth Catalyst stability Ostwald ripening Leaching Nickel catalysts Particle size effect Support effect 

摘      要：The deactivation behavior by crystallite growth of nickel nanoparticles on various supports（carbon nanofibers, zirconia, Si C, α-Al2O3 and γ-Al2O3） was investigated in the aqueous phase reforming of ethylene glycol. Supported Ni catalysts of ~10 wt% were prepared by impregnation of carbon nanofibers（CNF）,Zr O2, SiC, γ-Al2O3 and α-Al2O3. The extent of the Ni nanoparticle growth on various support materials follows the order CNF ~ ZrO2〉 SiC 〉 γ-Al2O3〉〉 α-Al2O3 which sequence, however, was determined by the initial Ni particle size. Based on the observed nickel leaching and the specific growth characteristics; the particle size distribution and the effect of loading on the growth rate, Ostwald ripening is suggested to be the main mechanism contributing to nickel particle growth. Remarkably, initially smaller Ni particles（~12 nm） supported on α-Al2O3 were found to outgrow Ni particles with initially larger size（~20 nm）. It is put forward that the higher susceptibility with respect to oxidation of the smaller Ni nanoparticles and differences in initial particle size distribution are responsible for this behavior.