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Modifications to sorption and sinking capability of microplastics after chlorination
Chlorination disinfection in water treatments may be highly destructive to microplastics (MPs). Herein, low- and high-dose (concentration–time values at 75 and 9,600 mg min L−1, respectively) chlorination processes were used to simulate short-term chlorination in drinking water treatment plants and long-term residual chlorine reaction in drinking water supply systems, respectively. Both chlorination processes induced modifications to polyethylene (PE), polyethylene terephthalate (PET), polystyrene (PS), and polyvinyl chloride (PVC) MPs, varying in polymer types and sizes. Oxidized and chlorinated bonds were detected, and destructed surfaces with increased specific surface area and reduced hydrophobicity were observed. As a result, the sorption capacity of all MPs was weakened, e.g., low-dose chlorination (pH 7) depressed the sorption of ciprofloxacin by 6.5 μm PE (Kf from 0.140 to 0.128 L g−1). The sinking behavior of PET, PS, and PVC MPs was enhanced, e.g., the sinking ratio of 200 μm PET increased by ∼30% after low-dose chlorination (pH 7). By contrast, PE tended to float after high-dose chlorination. Furthermore, chlorination of MPs generated various products, which were the degraded fragments from the MP skeleton. In general, chlorination disinfection reduces the potential of MPs as transport vectors of organic contaminants. HIGHLIGHTS Disinfection by chlorination is destructive to microplastics (MPs).; MPs tend to adsorb less ciprofloxacin after chlorination.; MPs, except polythene, tend to sink after chlorination.; Chlorination reduces the potential of MPs as transport vectors of organic contaminants.; Practical dose chlorination presents limited effects on MPs.;
Modifications to sorption and sinking capability of microplastics after chlorination
Chlorination disinfection in water treatments may be highly destructive to microplastics (MPs). Herein, low- and high-dose (concentration–time values at 75 and 9,600 mg min L−1, respectively) chlorination processes were used to simulate short-term chlorination in drinking water treatment plants and long-term residual chlorine reaction in drinking water supply systems, respectively. Both chlorination processes induced modifications to polyethylene (PE), polyethylene terephthalate (PET), polystyrene (PS), and polyvinyl chloride (PVC) MPs, varying in polymer types and sizes. Oxidized and chlorinated bonds were detected, and destructed surfaces with increased specific surface area and reduced hydrophobicity were observed. As a result, the sorption capacity of all MPs was weakened, e.g., low-dose chlorination (pH 7) depressed the sorption of ciprofloxacin by 6.5 μm PE (Kf from 0.140 to 0.128 L g−1). The sinking behavior of PET, PS, and PVC MPs was enhanced, e.g., the sinking ratio of 200 μm PET increased by ∼30% after low-dose chlorination (pH 7). By contrast, PE tended to float after high-dose chlorination. Furthermore, chlorination of MPs generated various products, which were the degraded fragments from the MP skeleton. In general, chlorination disinfection reduces the potential of MPs as transport vectors of organic contaminants. HIGHLIGHTS Disinfection by chlorination is destructive to microplastics (MPs).; MPs tend to adsorb less ciprofloxacin after chlorination.; MPs, except polythene, tend to sink after chlorination.; Chlorination reduces the potential of MPs as transport vectors of organic contaminants.; Practical dose chlorination presents limited effects on MPs.;
Modifications to sorption and sinking capability of microplastics after chlorination
Xinni Wu (author) / Mingjun Fan (author) / Zongyi Tan (author) / Ruijuan Liu (author) / Zhianqi Liao (author) / Eddy Y. Zeng (author) / Huase Ou (author)
2023
Article (Journal)
Electronic Resource
Unknown
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