Catalytic oxidation of n-hexane promoted by Ce1-xCuxO2 catalysts prepared by one-step polymeric precursor method

被引:11
作者
Araujo, Vinicius D. [1 ]
de Lima, Mauricio M., Jr. [2 ,3 ]
Cantarero, Andres [2 ]
Bernardi, Maria I. B. [1 ]
Bellido, Jorge D. A. [4 ]
Assaf, Elisabete M. [5 ]
Balzer, Rosana [6 ]
Probst, Luiz F. D. [6 ]
Fajardo, Humberto V. [7 ]
机构
[1] Univ Sao Paulo, Inst Fis, BR-13560970 Sao Carlos, SP, Brazil
[2] Univ Valencia, Inst Ciencia Mat, E-46071 Valencia, Spain
[3] Univ Valencia, Fdn Gen, Valencia, Spain
[4] Univ Fed Sao Joao Del Rei UFSJ, CAP Engn Quim, Sao Joao Del Rei, MG, Brazil
[5] Univ Sao Paulo, Inst Quim, BR-13560970 Sao Carlos, SP, Brazil
[6] Univ Fed Santa Catarina UFSC, Dept Quim, BR-88040900 Florianopolis, SC, Brazil
[7] Univ Fed Ouro Preto UFOP, Dept Quim, BR-35400000 Ouro Preto, MG, Brazil
基金
巴西圣保罗研究基金会;
关键词
Ceramics; Chemical synthesis; Oxides; Oxidation; NANOCOMPOSITE CATALYSTS; CO; OXIDE; CEO2; PHOTOLUMINESCENCE; PLATINUM; ETHANOL; FE;
D O I
10.1016/j.matchemphys.2013.08.021
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Ceria-supported copper catalysts (Ce(1-x)Cu(x)O2, with x (mol) = 0, 0.01, 0.03, 0.05 and 0.10) were prepared in one step through the polymeric precursor method. The textural properties of the catalysts were investigated by X-ray diffraction (XRD), Rietveld refinement, N-2-physisorption (BET surface area), electron paramagnetic resonance (EPR), UV visible diffuse reflectance and photoluminescence spectroscopies and temperature-programmed reduction (TPR). In a previous study ceria-supported copper catalysts were found to be efficient in the preferential oxidation of CO. In this study, we extended the catalytic application of Ce(1-x)Cu(x)O2 systems to n-hexane oxidation and it was verified that the catalysts were highly efficient in the proposed reaction. The best performance (up to 95% conversion) was observed for the catalysts with low copper loads (Ce(0.92)Cu(0.03)O2 and Ce(0.99)Cu(0.01)O2, respectively). The physicochemical characterizations revealed that these behaviors could be attributed to the copper species present in the catalysts and the interaction between CuO and CeO2, which vary according to the copper content. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:677 / 681
页数:5
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