催化作用
双金属片
一氧化碳
贵金属
甲苯
吸附
过渡金属
金属
纳米颗粒
工业催化剂
催化氧化
化学工程
材料科学
无机化学
纳米材料基催化剂
化学
分散性
催化剂载体
纳米技术
有机化学
工程类
作者
Peng Peng,Jun Li,Shengpeng Mo,Qi Zhang,Taiming Shen,Qinglin Xie
出处
期刊:Processes
[Multidisciplinary Digital Publishing Institute]
日期:2021-01-26
卷期号:9 (2): 230-230
被引量:24
摘要
Carbon monoxide (CO) and hydrocarbons (HCs) generally have competitive adsorption on the active site of noble-metal nano-catalysts, thus developing an effective way to reduce the passivation of competitive reaction with each other is an urgent problem. In this study, we successfully synthesized transition metal-noble metal (Pt-M) alloys via introducing inexpensive metal elements (M = Ni, Co and Cu) into Pt particles and then deposited on alumina support to form Pt-based catalysts. Subsequently, we choose CO and toluene as polluting gases to evaluate the catalytic activities of Pt-M/Al2O3 catalysts. Introducing inexpensive metal elements (M = Ni, Co, and Cu) significantly changed the physicochemical properties and catalytic activities of these Pt-based catalysts. It can be found that the Pt-Co/Al2O3 catalyst exhibited outstanding catalytic activity for CO and toluene oxidation under mixed gas atmosphere, compared with other Pt-based catalysts, which is due to the higher dispersity, more surface adsorption oxygen, and well redox ability. Surprisingly, H2O could promote the catalytic activities for CO/toluene co-oxidation over the Pt-Co/Al2O3 catalyst. Thus, the present synthetic strategy not only opens an avenue towards the synthesis of noble metal-based catalysts, but also provides an excellent tolerance to H2O in the catalytic process.
科研通智能强力驱动
Strongly Powered by AbleSci AI