Studies on the activation of hydrogen peroxide for color removal in the presence of a new Cu(II)-polyampholyte heterogeneous catalyst

被引:59
作者
Lazaro Martinez, Juan Manuel [1 ]
Leal Denis, Maria Florencia [2 ]
Leonor Piehl, Lidia [3 ]
Rubin de Celis, Emilio [3 ]
Yolanda Buldain, Graciela [1 ]
Dall' Orto, Viviana Campo [2 ]
机构
[1] Univ Buenos Aires, Fac Farm & Bioquim, Dept Quim Organ, Ciudad Autonoma Buenos A, Argentina
[2] Univ Buenos Aires, Fac Farm & Bioquim, Dept Quim Analit & Fisicoquim, Ciudad Autonoma Buenos A, Argentina
[3] Univ Buenos Aires, Fac Farm & Bioquim, Dept Fisicomatemat, Ciudad Autonoma Buenos A, Argentina
关键词
heterogeneous catalyst; copper ion; hydrogen peroxide; azo dyes; ESR;
D O I
10.1016/j.apcat6.2008.01.030
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
In this work we describe the application of a new non-soluble and non-porous complex with copper ion based on ethylene glycol diglycidyl ether (EGDE), methacrylic acid (MAA) and 2-methylimidazole (2MI) in the decolorization of an azo dye Methyl Orange (MO) as a model pollutant at room temperature. The complex with copper ion was studied by ESR and SEM and was tested as a heterogeneous catalyst for H2O2 activation. A possible mechanism of interaction involves the production of hydroxyl radicals (confirmed by ESR), dioxygen and water. The Cu(II)-polyampholyte/H2O2 system acted efficiently in the color removal of MO. The adsorption and oxidative degradation of the azo-based dye followed pseudo-first-order kinetic profiles, and the rate constant for degradation had a second-order dependence on copper ion content in the mixture. A removal of MO higher than 90% was achieved in 20 min at pH 7.0. combining 0.8 mM of complexed copper ions in the mixture with 24 mM hydrogen peroxide. The dye adsorbed on the polyampholyte following a L4-type isotherm with 4.9 mu mol g(-1) maximum loading capacity and 3.1 mu M dissociation constant for the first monolayer. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:273 / 283
页数:11
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