In situ redispersion of rhodium nanocatalyst for CO2 reforming of CH4

被引:17
作者
Fu, Yu [1 ]
Kong, Wenbo [1 ]
Pan, Bingrong [1 ]
Yuan, Changkun [1 ]
Li, Shuqing [1 ]
Zhu, He [1 ]
Zhang, Jun [1 ]
机构
[1] Chinese Acad Sci, Shanghai Adv Res Inst, CAS Key Lab Low Carbon Convers Sci & Engn, Shanghai 201412, Peoples R China
来源
JOURNAL OF ENVIRONMENTAL CHEMICAL ENGINEERING | 2021年 / 9卷 / 04期
基金
中国国家自然科学基金;
关键词
Noble metals; Deactivation; Titania; Heat treatment; Hydrocarbons; METAL-SUPPORT INTERACTIONS; SINGLE-ATOM CATALYST; CARBON-DIOXIDE; SYNTHESIS GAS; RE-DISPERSION; METHANE; REDUCTION; STABILITY; PLATINUM; TEMPERATURE;
D O I
10.1016/j.jece.2021.105790
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Noble metal nanoparticles (NPs) exhibit high reactivity towards hydrocarbon reforming, however, suffer from agglomeration and poisoning issues (e.g., carbon deposition). A facile and environmental approach to rejuvenate noble metal catalysts is techniques using thermal redox cycles. Here we demonstrate that in situ thermal oxidative aging and reduction strategy can reverse the sintering of Rh/TiO2 catalyst and meanwhile this redox process significantly affects the catalytic performance towards methane dry reforming (DRM). The oxidative aging process has substantial impact on the mobilization of Rh species across TiO2, and thus the degree of oxymetal activation and the Rh NPs size. In the subsequent reductive process, reduction temperature not only influences oxymetal activation but also the electronic structure of Rh NPs, which directly relates to the carbon formation.
引用
收藏
页数:8
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