Preparation of MgAlY-LDO Solid Base Catalysts and their Catalytic Performance on the Synthesis of Isophorone via Acetone Condensation

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Abstract:

Mg-Al composite oxide (MgAlY-LDO) solid base catalysts were prepared via the coprecipitation method, followed by calcinations at high temperatures. Isophorone synthesis from acetone condensation was also investigated. The catalysts were characterized via X-ray diffraction analysis, Fourier transform infrared spectroscopy, CO2 temperature-programmed desorption, and Brunauer-Emmett-Teller analysis. After doping with Y, the MgAl-LDO showed higher catalytic activity at a reaction temperature of 300 °C, 100 kPa and WHSV 6.3 h-1. Furthermore, the conversion of acetone and the selectivity of isophorone increased from 17.8% and 11.0% to 37.5% and 58.7%, respectively. These results indicate that the basicity of MgAlY-LDO as well as the number of its strong base centers increased after Y doping. The pore volume and size of MgAlY-LDO increased because of the increased hydrotalcite layer space caused by the big Y3+ ion. However, the crystal structure of hydrotalcite was remained. Y2O3 was evenly dispersed in MgAlY-LDO at low Y doping amounts. As the doping amount increased, the layer structure of hydrotalcite became distorted, thereby affecting the crystallinity of the hydrotalcite. Some Y3+ ions emerged from the Mg2+ lattice after doping with a high Y3+ concentration.

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Periodical:

Advanced Materials Research (Volumes 550-553)

Pages:

424-428

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July 2012

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[1] S. Kannan: Catalysis Surveys from Asia Vol. 10(2006), p.117

Google Scholar

[2] H. C. Greenwell, P. J. Holliman, W. Jones, and B. V. Velasco: Catal. Today Vol. 114(2006), p.397

Google Scholar

[3] Y. Liu, K. Sun, H. Ma, X. Xu, and X. Wang: Catal. Commun. Vol. 11(2010), p.880

Google Scholar

[4] Q.-Q. Yu, S. Wang, R.-X. Bai, F.-M. Mei, and G.-X. Li: Chemical Journal of Chinese Universities-Chinese Vol. 26(2005), p.1502

Google Scholar

[5] L. Wang, X. Meng, and F. Xiao: Chinese Journal of Catalysis Vol. 31(2010), p.943

Google Scholar

[6] C.-h. Zhou, X. Hua-li, Z.-x. Du, Y.-x. Fan, Z.-h. Ge, and X.-n. Li: Journal of Chemical Engineering of Chinese Universities Vol. 23(2009), p.516

Google Scholar

[7] F. Shi, H. Gu, Y. Li, D. Wang, and L. Zhang: Chinese Journal of Catalysis Vol. 30(2009), p.201

Google Scholar

[8] Z.-M. Ni, S.-J. Xia, L.-G. Wang, F.-F. Xing, and G.-X. Pan: J. Colloid Interface Sci. Vol. 316(2007), p.284

Google Scholar

[9] W. Cheng, W. Wang, Y. Zhao, L. Liu, L. Shao, and J. Yang: J. Chem. Ind. Eng.(China) Vol. 58(2007), p.3072

Google Scholar

[10] A. E. Palomares, G. Eder-Mirth, M. Rep, and J. A. Lercher: J. Catal. Vol. 180(1998), p.56

Google Scholar

[11] Z.-l. Liu, Y. Liu, and B.-l. Lu: Journal of Guangzhou University (Natural Science Edition) Vol. 10(2011), p.14

Google Scholar

[12] T. Feng, D.-Q. Li, D. G. Evans, and X. Duan: Chinese Journal of Inorganic Chemistry Vol. 18(2002), p.1156

Google Scholar

[13] Z.-q. Guo, Z.-m. Ni, C.-p. Fang, W.-h. Yu, L.-g. Wang, and Z.-h. Ge: Journal of Zhejiang University of Technology Vol. 33(2005), p.102

Google Scholar

[14] B. Zapata, P. Bosch, G. Fetter, M. A. Valenzuela, J. Navarrete, and V. H. Lara: Int. J. Inorg. Mater. Vol. 3(2001), p.23

Google Scholar

[15] Y.-M. Xu: Chemical Journal of Chinese Universities-Chinese Vol. 20(1999), p.670

Google Scholar