The Study of the Degradation of the Phosphate Ester Catalyzed by the Nitrogen Unsaturated Heterocycle Cerium(III) Complex

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Abstract:

Phosphate ester and its ramifications in the pesticide are virulent and some are known to be human carcinogens. The removal of phosphate ester in the leftover of the pesticide has been a major environmental concern. The Cerium(III) complex made up of a nitrogen unsaturated heterocycle ligand and Cerium ion(III) was used in the catalytic degradation of bis(4-nitrophenyl) phosphate ester (BNPP). This catalytic system showed higher catalytic activity and better reproducibility and stability than other similar Cerium(III) systems. The rate of the BNPP catalytic degradation was about 109 -fold faster than that of its spontaneous degradation at the same conditions. The Cerium(III) complex is an very effective catalyst in the degradation of the phosphate ester.

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Advanced Materials Research (Volumes 518-523)

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541-544

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May 2012

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© 2012 Trans Tech Publications Ltd. All Rights Reserved

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[1] S. H. Gellman, R. Petter, R. Breslow: J. Am. Chem. Soc. Vol. 108(1986), p.2388

Google Scholar

[2] P. E. Jurek, A. M. Jurek, A. E. Martell: Inorg. Chem. Vol.39(2000), p.1016

Google Scholar

[3] C. M. Hartshorn, J. R. Deschamps, A. Singh: React. Funct. Polym. Vol.55(2003), p.219

Google Scholar

[4] E. Longhinotti, J. B. Domingos, B. Szpoganicz: Inorg. Chim. Acta. Vol.358(2005), p.(2089)

Google Scholar

[5] C.Vichard and T.A. Kaden: Inorg. Chim. Acta. Vol.357(2004), p.2285

Google Scholar

[6] J. Zhang, Y.Tang, J. Q. Xie: Acta. Phys. Chim. Sin. Vol.21(2005), p.408

Google Scholar

[7] W.D. Jiang, B. Xu, J. B. Zhong: J. Chem. Sci. Vol.120(2008), p.411

Google Scholar

[8] S. Couderc, J. Toullec: Langmuir Vol.17(2001), p.3819

Google Scholar

[9] J. Du, Y. Jiang, X .M. Kou: J. Colloid. Interf. Sci. Vol.256( 2002), p.428

Google Scholar

[10] W.D. Jiang, Z. Huang, F.A. Liu: Trnnsition. Met. Chem. Vol.25(2004): p.819

Google Scholar

[11] G.D. Lei, J.Q. Xie, C. Li: Trans. Met. Chem. Vol.33(2008), p.655

Google Scholar

[12] E.L. Hegg, S.H. Mortimore, C. L. Cheung: Irong. Chem. Vol.38(1999), p.2961

Google Scholar

[13] G.T. Paola and A.K. Yatsimirsky: J. Chem. Soc. Dalton. Trans. (1998), p.2957

Google Scholar

[14] A.L. Maldonado and A.K. Yatsimirsky: Org. Biomol. Chem. Vol. 3(2005), p.2859

Google Scholar

[15] J. S. Li and B. Xie: Acta Chim Sin, Vol.55(1997), p.892

Google Scholar

[16] M.J. Young, D. Wahnon, R. C. Hynes: J. Am. Chem. Soc. Vol.117(1995), p.9441

Google Scholar