Peroxymonosulfate assisted mechanochemical remediation of high concentration DDTs contaminated soil.

DDTs (DDT and its metabolites) contaminated sites urgently need to be treated efficiently and greenly. In this study, a horizontal planetary mechanochemical method with co-milling additives was developed aiming at efficiently degrading high-concentration DDTs in historical contaminated soil (∼7500 mg/kg). Peroxymonosulfate (PMS) was firstly used to the mechanochemical degradation of DDTs in historical contaminated soil, with a degradation efficiency of over 95% after 1 h of milling under the optimal milling conditions (CR = 30:1, r = 500 rpm, R = 1:4). Mechanism study indicated that DDTs in soil were partially dechlorinated and mineralized. The main products formed might be chlorinated aliphatic hydrocarbons, which need further treatment by ball milling or other methods. Under the action of mechanical energy, PMS could oxidize DDTs in soil through non-radical way rather than common radical way. Then, a comprehensive assessment of this remediation method was conducted by analyzing the changes in soil properties and acute biotoxicity after ball milling. Although PMS had a great performance on the degradation of DDTs, especially p, p'-DDE, it would cause the acidification and salinization of soil. Therefore, further pH adjustment and desalination treatment were suggested to reduce the negative impacts. This work successfully presents a practical approach to mechanochemical remediation of DDTs contaminated sites.

Mechanochemical remediation of lindane-contaminated soils assisted by CaO: Performance, mechanism and overall assessment.

Soil contamination caused by persistent organic pollutants (POPs) has been a worldwide concern for decades. With lindane-contaminated soil as the target, a mechanochemical method assisted by CaO was comprehensively evaluated in terms of its remediation performance, degradation mechanism and overall assessment. The mechanochemical degradation performance of lindane in cinnamon soil or kaolin was determined under different additives, lindane concentrations and milling conditions. 2,2-Diphenyl-1-(2,4,6-trinitrophenyl) hydrazinyl free radical (DPPH•) and electron spin resonance (ESR) tests evidenced that the degradation of lindane in soil was caused mainly by the mechanical activation of CaO to produce free electrons (e-) and the alkalinity of the generated Ca(OH)2. Dehydrochlorination or dechlorination by elimination, alkaline hydrolysis, hydrogenolysis and the subsequent carbonization were the main degradation pathways of lindane in soil. The main final products included monochlorobenzene, carbon substances and methane. The mechanochemical method with CaO was proved to also efficiently degrade lindane in three other soils and other hexachlorocyclohexane isomers and POPs in soil. The soil properties and soil toxicity after remediation were assessed. This work presents a relatively clear discussion of various aspects of the mechanochemical remediation of lindane-contaminated soil assisted by CaO.

Horizontal planetary mechanochemical method for rapid and efficient remediation of high-concentration lindane-contaminated soils in an alkaline environment.

Lindane is a persistent organic pollutant that has attracted worldwide attention because of its threat to human health and environmental security. A horizontal planetary mechanochemical method was developed for rapid and efficient degradation of lindane in soil in an alkaline environment. Under the condition of a very low reagent-to-soil ratio (R = 2%), ball-to-powder ratio (CR = 6:1), rotation speed (r = 300 rpm) and high soil single treatment capacity (SC = 60 g), the lindane in four typical soils (~ 100 mg/kg) can be degraded up to 96.30% in 10 min. This method can also remediate high-concentration lindane-contaminated soil (833 ± 26 mg/kg). The experimental results and theoretical calculations proved that the stepwise dechlorination and final carbonization of lindane in soil are mainly attributed to the combined action of mechanical energy and alkalinity. The bimolecular elimination (E2) reaction was the first step of lindane destruction. Subsequently, the unimolecular elimination (E1) reaction tended to occur with the weakening of alkalinity. Then, benzene was obtained through stepwise hydrogenolysis reaction. The last was the generation of carbon substances by fragmentation or condensation of benzene rings. This work proposes a practical remediation technology for organic contaminated soil and improves the understanding of the degradation pathways of lindane in soil in alkali-assisted mechanochemical system.