Thermally activated peroxydisulfate in the presence of additives: A clean method for the degradation of pollutants

被引:98
作者
Mora, Veronica C. [1 ]
Rossoa, Janina A. [1 ]
Carrillo Le Roux, Galo [2 ]
Martire, Daniel O. [1 ]
Gonzalez, Monica. C. [1 ]
机构
[1] Univ Nacl La Plata, CONICET, INIFTA, Fac Ciencias Exactas, RA-1900 La Plata, Argentina
[2] Univ Sao Paulo, Escola Politecn, Dept Engn Quim, Sao Paulo, Brazil
关键词
Carbon dioxide radical anions; Sulfate radicals; Trichloroacetic acid; Waste water treatment; Activated peroxydisulfate; PERSULFATE OXIDATION; AQUEOUS-SOLUTIONS; RADICALS; TRICHLOROETHYLENE; KINETICS; TCE; PHOTOLYSIS; ANIONS; SO4;
D O I
10.1016/j.chemosphere.2009.02.038
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The kinetics and mechanism of the thermal activation of peroxydisulfate, in the temperature range from 60 to 80 degrees C, was investigated in the presence and absence of sodium formate as an additive to turn the oxidizing capacity of the reaction mixture into a reductive one. Trichloroacetic acid, TCA, whose degradation by a reductive mechanism is well reported in the literature, was used as a probe. The chemistry of thermally activated peroxydisulfate is described by a reaction scheme involving free radical generation. The proposed mechanism is evaluated by a computer simulation of the concentration profiles obtained under different experimental conditions. In the presence of formate, SO4 center dot- radicals yield CO2 center dot-, which are the main species available for degrading TCA. Under the latter conditions, TCA is more efficiently depleted than in the absence of formate, but otherwise identical conditions of temperature and [S2O82-]. We therefore conclude that activated peroxydisulfate in the presence of formate as an additive is a convenient method for the mineralization of substrates that are refractory to oxidation. such as perchlorinated hydrocarbons and TCA. This method has the advantage that leaves no toxic residues. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1405 / 1409
页数:5
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