Kargar Mahdi, Nabizadeh Ramin, Naddafi Kazem, Nasseri Simin, Mesdaghinia Alireza, Mahvi Amir Hossein, Alimohammadi Mahmood, Nazmara Shahrokh, Pahlevanzadeh Bagher
Department of Environmental Health Engineering, School of public Health, Tehran University of Medical Sciences, Tehran, Iran.
Iranian J Environ Health Sci Eng. 2012 Dec 23;9(1):32. doi: 10.1186/1735-2746-9-32.
Sonolysis and photochemical degradation of different compounds such as chlorinated aliphatic hydrocarbons are among the recent advanced oxidation processes. Perchloroethylene is one of these compounds that has been mainly used as a solvent and degreaser. In this work, elimination of perchloroethylene in aqueous solution by ultrasonic irradiation, andphotochemical oxidation by ultra violet ray and hydrogen peroxide were investigated. Three different initial concentrations of perchloroethylene at different pH values, detention periods, and concentrations of hydrogen peroxide were investigated. Head space gas chromatography with FID detector was used for analyses of perchloroethylene. This research was performed in 9 months from April through December 2011.Results showed that perchloroethylene could be effectively and rapidly degraded by ultrasonic irradiation, photochemical oxidation by ultra violet ray, hydrogen peroxide and a combination of these methods. Kinetics of perchloroethylene was strongly influenced by time, initial concentration and pH value. Degradation of Perchloroethylene increased with decrease in the initial concentration of perchloroethylene from 0.3 to 10 mg/L at all initial pH. The results showed an optimum degradation condition achieved at pH = 5 but did not affect significantly the perchloroethylene destruction in the various pH values. Kinetic modeling applied for the obtained results showed that the degradation of perchloroethylene by ultrasound and photo-oxidation followed first order and second order model. The percentage of removal in the hybrids reactor was higher than each of the reactors alone, the reason being the role of hydroxyl radical induced by ultrasound and photochemical reaction.
声解以及光化学降解不同化合物(如氯代脂肪烃)属于近期的高级氧化过程。全氯乙烯是这些化合物之一,主要用作溶剂和脱脂剂。在本研究中,考察了通过超声辐照去除水溶液中的全氯乙烯,以及紫外线和过氧化氢进行的光化学氧化作用。研究了在不同pH值、停留时间和过氧化氢浓度下三种不同初始浓度的全氯乙烯。采用配有FID检测器的顶空气相色谱法分析全氯乙烯。本研究于2011年4月至12月的9个月内进行。结果表明,全氯乙烯可通过超声辐照、紫外线光化学氧化、过氧化氢以及这些方法的组合被有效且快速地降解。全氯乙烯的动力学受时间、初始浓度和pH值的强烈影响。在所有初始pH值下,随着全氯乙烯初始浓度从0.3降至10 mg/L,其降解率增加。结果表明,在pH = 5时达到最佳降解条件,但在不同pH值下对全氯乙烯的破坏影响不显著。对所得结果应用动力学模型表明,超声和光氧化降解全氯乙烯遵循一级和二级模型。混合反应器中的去除率高于单独的每个反应器,原因是超声和光化学反应诱导产生的羟基自由基的作用。