4.8 Article

Microplastic removal in conventional drinking water treatment processes: Performance, mechanism, and potential risk

Journal

WATER RESEARCH
Volume 202, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.watres.2021.117417

Keywords

Microplastics; Drinking water treatment system; Coagulation; Sand filtration; Advanced oxidation; Toxicity

Funding

  1. National Research Foundation of Korea (NRF) - Korea government [2019R1A2C2003064]
  2. Korea Environment Industry & Technology Institute (KEITI) - Korea Ministry of Environment (MOE) [2020003110004]
  3. Korea Institute of Science and Technology institutional programs [2E30503, 2E31261]
  4. National Research Foundation of Korea [2019R1A2C2003064] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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The study found that the removal efficiency of microplastics in traditional drinking water treatment plants is influenced by the size of microplastics, the type of coagulant, and water characteristics. They used X-ray microcomputed tomography technique and two-site kinetic modeling to discover that microplastics below 20 microns were retained by attachment to the sand surface.
The effectiveness of traditional drinking water treatment plants for the removal of Microplastics (MPs) in the size range of tens of micrometers is currently uncertain. This study investigated the behavior and removal efficiency of four different sized polystyrene MPs (10-90 mu m in diameter) in a simulated cascade of coagulation/sedimentation, sand filtration, and UV-based oxidation over technically relevant time frames. In the coagulation and sand filtration steps, the larger the MP size, the better it was removed. The coagulant type and water characteristics (i.e., pH and the presence of natural organic matter) influenced the coagulation efficiency for MPs. X-ray microcomputed tomography technique and two-site kinetic modeling were used to identify the mechanisms involved in sand filtration. The MPs 20 mu m could be completely retained in sand by straining, while the attachment to the sand surface was likely responsible for the retention of MPs < 20 mu m. However, approximately 16% of 10 mu m MPs injected passed through the sand, which were further fragmented by UV oxidation. UV/H2O2 treatment promoted the MP fragmentation and chemical leaching more significantly than UV treatment, resulting in a higher toxicity for UV/H2O2-treated water. Our findings pave the way for deeper understanding of how MPs behave and transform in a sequential drinking water treatment process.

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