Investigation of the physicochemical properties of CuO/Sm2O3/γ-Al2O3 catalysts and their activity for NO removal by CO

被引:20
作者
Lv, Yuanyuan [1 ,2 ]
Zhang, Hongliang [4 ]
Yao, Xiaojiang [2 ]
Dong, Lin [2 ,3 ]
Chen, Yi [2 ]
机构
[1] Wujiang Entry Exit Inspect & Quarantine Bur Peopl, Suzhou 215200, Peoples R China
[2] Nanjing Univ, Sch Chem & Chem Engn, Key Lab Mesoscop Chem MOE, Nanjing 210093, Jiangsu, Peoples R China
[3] Nanjing Univ, Ctr Modern Anal, Jiangsu Key Lab Vehicle Emiss Control, Nanjing 210093, Jiangsu, Peoples R China
[4] Anhui Univ Technol, Anal & Testing Cent Facil, Maanshan 243002, Peoples R China
基金
中国国家自然科学基金;
关键词
CuO/gamma-Al2O3; Sm2O3; NO-CO reaction; Incorporation model; COPPER-OXIDE; INFRARED CHARACTERIZATION; CARBON-MONOXIDE; OXIDATION; DECOMPOSITION; CU; IDENTIFICATION; SPECTROSCOPY; GAMMA-AL2O3; ADSORPTION;
D O I
10.1016/j.molcata.2016.03.038
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
XRD, LRS, H-2-TPR, and in situ FT-IR techniques were employed to investigate the dispersion, physicochemical behaviors of the Sm2O3 modification for CuO/gamma-Al2O3 catalysts. And the catalytic performance for CuO/Sm2O3/gamma-Al2O3 catalysts was tested by NO-CO reaction. The results indicated that (1) samarium oxide could be dispersed on the surface of gamma-Al2O3 with a dispersion capacity of about 0.625 mmol/100 m(2) and the supported copper oxide could be also dispersed upon the surface of Sm2O3/gamma-Al2O3; (2) the reducibility of copper oxide was inhibited by the presence of samarium oxide, which could be influenced by the loading amounts of Sm2O3 upon gamma-Al2O3 surface; (3) FT-IR results implied that the presence of samarium oxide species made the copper oxide hard to be reduced by CO while enhanced the NO strongly adsorbed; (4) NO-CO reaction could start to react only when both of them were in adsorbed states and the formation of free-like NO3- species was recognized as the intermediates of the reaction; (5) the reaction activity was negatively influenced by the introduction of samarium oxide in CuO/gamma-Al2O3 catalysts. And a possible reaction pathway was tentatively proposed to discuss the NO-CO reaction based on all of these results. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:34 / 44
页数:11
相关论文
共 47 条
[1]   Infrared characterization of Rh surface states and their adsorbates during the NO-CO reaction [J].
Almusaiteer, KA ;
Chuang, SSC .
JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (10) :2265-2272
[2]   One-electron reducibility of isolated copper oxide on alumina for selective NO-CO reaction [J].
Amano, Fumiaki ;
Suzuki, Sosuke ;
Yamamoto, Takashi ;
Tanaka, Tsunehiro .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2006, 64 (3-4) :282-289
[3]   DETERMINATION OF THE PREFERENTIAL EXPOSED PLANE OF POWDERED SUPPORTS OF CATALYSTS BY DIFFERENTIAL NEUTRON-DIFFRACTION [J].
BEAUFILS, JP ;
BARBAUX, Y .
JOURNAL DE CHIMIE PHYSIQUE ET DE PHYSICO-CHIMIE BIOLOGIQUE, 1981, 78 (04) :347-352
[4]   Adsorption of NO and CO over transition-metal-incorporated mesoporous catalytic materials [J].
Bhargava, SK ;
Akolekar, DB .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2005, 281 (01) :171-178
[5]   METHANE ACTIVATION BY THE LANTHANIDE OXIDES [J].
CAMPBELL, KD ;
ZHANG, H ;
LUNSFORD, JH .
JOURNAL OF PHYSICAL CHEMISTRY, 1988, 92 (03) :750-753
[6]   SURFACE INTERACTION-MODEL OF GAMMA-ALUMINA-SUPPORTED METAL-OXIDES [J].
CHEN, Y ;
ZHANG, LF .
CATALYSIS LETTERS, 1992, 12 (1-3) :51-62
[7]  
CHEN Y, 1991, CAT SCI TEC, V1, P291
[8]   Determination of the dispersion and surface oxidation states of supported Cu catalysts [J].
Dandekar, A ;
Vannice, MA .
JOURNAL OF CATALYSIS, 1998, 178 (02) :621-639
[9]   Anomalous high pressure behaviour in nanosized rare earth sesquioxides [J].
Dilawar, Nita ;
Varandani, Deepak ;
Mehrotra, Shalini ;
Poswal, Himanshu K. ;
Sharma, Surinder M. ;
Bandyopadhyay, Ashis K. .
NANOTECHNOLOGY, 2008, 19 (11)
[10]   Heats of adsorption of CO on a Cu/Al2O3 catalyst using FTIR spectroscopy at high temperatures and under adsorption equilibrium conditions [J].
Dulaurent, O ;
Courtois, X ;
Perrichon, V ;
Bianchi, D .
JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (25) :6001-6011