학술논문
Comparison of chlorination resistance of biodegradable microplastics and conventional microplastics during the disinfection process in water treatments.
Document Type
Academic Journal
Author
Zhang X; School of Environmental Science and Engineering, Tianjin University, Tianjin 300350, China.; Feng X; School of Environmental Science and Engineering, Tianjin University, Tianjin 300350, China.; Ma Y; School of Marine Science and Technology, Tianjin University, Tianjin 300072, China.; Niu Z; School of Environmental Science and Engineering, Tianjin University, Tianjin 300350, China; International Joint Institute of Tianjin University, Fuzhou, Fuzhou 350205, China.; Zhang Y; School of Environmental Science and Engineering, Tianjin University, Tianjin 300350, China. Electronic address: yzhang_n@tju.edu.cn.
Source
Publisher: Elsevier Country of Publication: Netherlands NLM ID: 0330500 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1879-1026 (Electronic) Linking ISSN: 00489697 NLM ISO Abbreviation: Sci Total Environ Subsets: MEDLINE
Subject
Language
English
Abstract
Nowadays, microplastics (MPs) widely exist in the environment, and water treatment plants are important sources of MPs. Chlorine is widely used in the disinfection process in water treatment plants and has strong oxidation, however, the chemical and physical properties changes of MPs during chlorination were unclear. Thus, in this study, based on the actual used chlorine concentrations, different chlorination conditions were simulated to study the variation of MPs after chlorination. Meanwhile, the produced disinfection by-products were monitored. The results showed that under high chlorination concentration conditions, functional groups of polyethylene (PE), polystyrene (PS), and polylactic acid (PLA) changed, while no peak shift or change of poly (butyleneadipate-co-terephthalate) (PBAT) could be detected. Moreover, after chlorination, partial yellowing and cracks appeared on PS, PLA, and PBAT, while PE remained white and showed little morphological changes. Besides, chlorination led to the narrowing of the cold crystallization peak and melting peak of PLA, while chlorination had little influence on the crystal structure of PE and PBAT. Furthermore, the reaction between PLA and chlorine mostly produced more trichloromethane than other types of MPs. Consequently, when chlorine concentrations were in the range of 2.5 to 5000 mg/L, the chlorination resistance was PBAT/PE > PLA > PS. Specifically, PBAT had the strongest chlorination resistance in terms of chemical properties, while PE had the strongest chlorination resistance in terms of physical properties. Therefore, the degradability of biodegradable MPs is not higher than that of conventional MPs in all cases. Moreover, it should be noted that most changes occurred only in high chlorine concentrations. Thus, neither conventional MPs nor biodegradable MPs can be completely degraded during the chlorination process in water treatments.
Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
(Copyright © 2023 Elsevier B.V. All rights reserved.)
Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
(Copyright © 2023 Elsevier B.V. All rights reserved.)