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Photochlorination-induced degradation of microplastics and interaction with Cr(VI) and amlodipine
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Researchers found that photochlorination during wastewater disinfection significantly degrades polyethylene, polypropylene, and polystyrene microplastics while altering their interactions with co-existing pollutants like chromium and pharmaceuticals, potentially affecting environmental fate.
Wastewater treatment plants (WWTPs) are the important source of microplastics (MPs) in the environment, and disinfection processes bear high potential to degrade MPs. This study investigated the physicochemical degradation, dissolved organic products and interaction with co-existed pollutants (heavy metal and pharmaceutical) on polyethylene (PE), polypropylene (PP) and polystyrene (PS) MPs during simulated disinfection processes. Compared to photo or chlorination, photochlorination significantly resulted in the physicochemical degradation, including morphology alteration, fragmentation, and chemical oxidation on PP and PS MPs, but showed relatively low effect on PE, indicating the different resistance among polymers to disinfected treatment. Photochlorination also caused the formation of chain-scission organic compounds and even chlorinated products from MPs (e.g. CHOCl for PP and monochlorophenol, dichlorophenol, chloroacetophenone and chlorobenzoic acid for PS), which may form disinfection byproducts to induce healthy risk. The adsorption potentials of MPs for Cr(VI) or amlodipine were enhanced by photochlorination since the cracking and formed oxygen functional groups enhanced the pore filling and surface precipitation of Cr(VI), and the electrostatic attraction and hydrogen bonding with amlodipine. The findings indicated the physicochemical degradation of MPs and the combined pollution with co-existed pollutants, highlighting the health risks of MP-derived organic products during the disinfection treatments (even in normal dosage) in WWTPs.
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Effects of chlorination on microplastics pollution: Physicochemical transformation and chromium adsorption
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Researchers found that chlorination of polyethylene and thermoplastic polyurethane microplastics significantly altered their surface morphology and oxygen-containing functional groups, enhancing their ability to aggregate and adsorb chromium contaminants in water.
The photo-redox of chromium regulated by microplastics (MPs) and MPs-derived dissolved organic matter (MPs-DOM) and the CO2 emission of MPs-DOM
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Researchers found that microplastics and their derived dissolved organic matter regulate the photo-redox transformation of chromium in wastewater, with UV exposure converting less toxic Cr(III) to more hazardous Cr(VI) while microplastic-derived organic matter influences this process and contributes to CO2 emissions.
Insight into the dynamic transformation properties of microplastic-derived dissolved organic matter and its contribution to the formation of chlorination disinfection by-products
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Researchers studied how dissolved organic matter released from microplastics transforms under UV light and how it contributes to the formation of harmful disinfection byproducts during water chlorination. They found that UV exposure changed the chemical composition of the microplastic-derived organic matter, affecting its reactivity during disinfection. The findings suggest that microplastics in water sources may indirectly increase the formation of potentially harmful chemicals during standard water treatment.
Chlorination of Antivirals in Wastewater: Effects of Microplastics and Ecotoxicity on Aquatic and Terrestrial Species
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Researchers investigated how microplastics affect the chlorination of antiviral pharmaceuticals in secondarily treated wastewater and assessed ecotoxicity of the resulting products. Microplastics altered chlorination byproduct formation and in some cases increased overall ecotoxicity of treated wastewater, suggesting that microplastic co-occurrence complicates pharmaceutical disinfection outcomes.
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