Conversion of Methane to Ethylene with BaCe0.9Y0.1CoxO3-δ Hydrogen Permeation Membrane

被引:0
作者
Liu Yun [1 ,2 ]
Yuan Sheng-Ze [2 ,3 ]
Xie Kui [2 ]
机构
[1] Fuzhou Univ, Coll Chem, Fuzhou 350116, Peoples R China
[2] Chinese Acad Sci, Key Lab Design & Assembly Funct Nanostruct, Fujian Inst Res Struct Matter, Fuzhou 350002, Peoples R China
[3] Fujian Normal Univ, Coll Chem & Mat Sci, Fuzhou 350007, Peoples R China
关键词
mixed-conducting; dehydrogenation; methane; metal nanoparticle; membrane; DEHYDROGENATION; NONSTOICHIOMETRY; ACTIVATION; CONDUCTORS; TRANSPORT; OLEFINS;
D O I
10.14102/j.cnki.0254-5861.2011-3055
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Dehydrogenation coupling of methane (DCM), which can be effectively used to produce low carbon alkenes, has the advantages of rich raw materials, simple reaction device, low energy consumption, etc. Herein, we report a series of Co doped perovskite porous-dense BaCe0.9Y0.1CoxO3-delta(BCYCx) membrane for DCM. After treatment in a reduced atmosphere, a large number of Co nanoparticles will exsolute on the surface of BCY. The metal-oxide interface is helpful to activate the C-H bonds, inhibit the carbon deposition, and so on. The XRD, SEM and XPS prove that Co nanoparticles homogeneously distributed on the BCYCx porous layers, which will create a large quantity of catalytic active sites. At 1100 C, the highest concentration of C-2 product was 5.66% (5.25% ethane + 0.41% ethylene) in output gas when methane conversion reaches a maximum value of 24.8%, and the C-2 selectivity gets to 45.6%. We further demonstrate the catalytic performance of high-temperature DCM without obvious decrease after running for 30 hours.
引用
收藏
页码:901 / 907
页数:7
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