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      Release Behavior of Liquid Crystal Monomers from Waste Smartphone Screens: Occurrence, Distribution, and Mechanistic Modeling

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          Abstract

          Liquid crystal display (LCD) screens can release many organic pollutants into the indoor environment, including liquid crystal monomers (LCMs), which have been proposed as a novel class of emerging pollutants. Knowing the release pathways and mechanisms of LCMs from various components of LCD screens is important to accurately assess the LCM release and reveal their environmental transport behavior and fate in the ambient environment. A total of 47, 43, and 33 out of 64 target LCMs were detected in three disassembled parts of waste smartphone screens, including the LCM layer (LL), light guide plate (LGP), and screen protector (SP), respectively. Correlation analysis confirmed LL was the source of LCMs detected in LGP and SP. The emission factors of LCMs from waste screen, SP, and LGP parts were estimated as 2.38 × 10 –3, 1.36 × 10 –3, and 1.02 × 10 –3, respectively. A mechanism model was developed to describe the release behaviors of LCMs from waste screens, where three characteristics parameters of released LCMs, including average mass proportion (AP), predicted subcooled vapor pressures ( P L), and octanol–air partitioning coefficients ( K oa), involving coexistence of absorption and adsorption mechanisms, could control the diffusion-partitioning. The released LCMs in LGP could reach diffusion-partition equilibrium more quickly than those in SP, indicating that LCM release could be mainly governed through SP diffusions.

          Abstract

          The diffusion-partitioning behaviors of LCMs released from various components of waste smartphone screens were modeled. The proposed release pathways and mechanisms provide valuable insights into the environmental transport behavior and fate of LCMs.

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          Transport and release of chemicals from plastics to the environment and to wildlife.

          Plastics debris in the marine environment, including resin pellets, fragments and microscopic plastic fragments, contain organic contaminants, including polychlorinated biphenyls (PCBs), polycyclic aromatic hydrocarbons, petroleum hydrocarbons, organochlorine pesticides (2,2'-bis(p-chlorophenyl)-1,1,1-trichloroethane, hexachlorinated hexanes), polybrominated diphenylethers, alkylphenols and bisphenol A, at concentrations from sub ng g(-1) to microg g(-1). Some of these compounds are added during plastics manufacture, while others adsorb from the surrounding seawater. Concentrations of hydrophobic contaminants adsorbed on plastics showed distinct spatial variations reflecting global pollution patterns. Model calculations and experimental observations consistently show that polyethylene accumulates more organic contaminants than other plastics such as polypropylene and polyvinyl chloride. Both a mathematical model using equilibrium partitioning and experimental data have demonstrated the transfer of contaminants from plastic to organisms. A feeding experiment indicated that PCBs could transfer from contaminated plastics to streaked shearwater chicks. Plasticizers, other plastics additives and constitutional monomers also present potential threats in terrestrial environments because they can leach from waste disposal sites into groundwater and/or surface waters. Leaching and degradation of plasticizers and polymers are complex phenomena dependent on environmental conditions in the landfill and the chemical properties of each additive. Bisphenol A concentrations in leachates from municipal waste disposal sites in tropical Asia ranged from sub microg l(-1) to mg l(-1) and were correlated with the level of economic development.
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            An absorption model of gas/particle partitioning of organic compounds in the atmosphere

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              Identifying new persistent and bioaccumulative organics among chemicals in commerce.

              The goal of this study was to identify commercial chemicals that might be persistent and bioaccumulative (P&B) and that were not being considered in current Great Lakes, North American, and Arctic contaminant measurement programs. We combined the Canadian Domestic Substance List (DSL), a list of 3059 substances of "unknown or variable composition complex reaction products and biological materials" (UVCBs), and the U.S. Environmental Protection Agency (U.S. EPA) Toxic Substances Control Act (TSCA) Inventory Update Rule (IUR) database for years 1986, 1990, 1994, 1998, 2002, and 2006 yielding a database of 22263 commercial chemicals. From that list, 610 chemicals were identified by estimates from U.S EPA EPISuite software and using expert judgment. This study has yielded some interesting and probable P&B chemicals that should be considered for further study. Recent studies, following up our initial reports and presentations on this work, have confirmed the presence of many of these chemicals in the environment.
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                Author and article information

                Journal
                Environ Sci Technol
                Environ Sci Technol
                es
                esthag
                Environmental Science & Technology
                American Chemical Society
                0013-936X
                1520-5851
                27 June 2023
                18 July 2023
                : 57
                : 28
                : 10319-10330
                Affiliations
                []School of Energy and Environment and State Key Laboratory of Marine Pollution, City University of Hong Kong , Hong Kong, China
                []Research Centre for the Oceans and Human Health, City University of Hong Kong Shenzhen Research Institute , Shenzhen 518057, China
                [§ ]Department of Chemistry and State Key Laboratory of Marine Pollution, City University of Hong Kong , Hong Kong, China
                []College of Environmental Science and Engineering, Nankai University , Tianjin 300350, China
                Author notes
                [* ]Email: henry.he@ 123456cityu.edu.hk . Tel: +852 3442-4370. Fax: +852 3442-0688.
                Author information
                https://orcid.org/0000-0001-7633-1701
                https://orcid.org/0000-0001-9211-4539
                Article
                10.1021/acs.est.2c09602
                10357588
                37369363
                fc0a8ce5-b74f-4479-b9f1-21128d252b5c
                © 2023 The Authors. Published by American Chemical Society

                Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works ( https://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 20 December 2022
                : 25 May 2023
                : 13 April 2023
                Funding
                Funded by: National Natural Science Foundation of China, doi 10.13039/501100001809;
                Award ID: 42177223
                Funded by: Marine Ecology and Enhancement Fund, doi NA;
                Award ID: MEEF2021002A
                Funded by: Guangdong Basic and Applied Basic Research Foundation, doi NA;
                Award ID: 2022A1515110549
                Funded by: Innovation and Technology Commission, doi 10.13039/501100003452;
                Award ID: NA
                Funded by: Research Grants Council, University Grants Committee, doi 10.13039/501100002920;
                Award ID: CityU 11311222
                Categories
                Article
                Custom metadata
                es2c09602
                es2c09602

                General environmental science
                liquid crystals monomers,emission factor,diffusion-partitioning,environmental modeling,release mechanism

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