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      Recent advances in plastic recycling and upgrading under mild conditions

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          Abstract

          This review summarizes the emerging advanced technologies including bio-, photo-, electro-, and low-temperature thermocatalysis for recycling and upgrading of waste plastics under mild conditions.

          Abstract

          Plastic depolymerization usually requires rigorous conditions such as high temperature, high pressure, and caustic bases or acids, resulting in high energy costs and environmental issues. Recently, new technologies that operate under mild conditions are emerging. This review summarizes the progress made in the past decade in the conversion of waste plastics into high-purity monomers or value-added products under mild conditions by bio-, photo-, electro-, and low-temperature thermocatalysis. First, the enzymatic depolymerization of plastics is discussed, with emphasis on the progress in enzyme engineering to improve the thermal stability of enzymes. Next, electro- and photocatalytic approaches for the conversion of waste plastics into high value-added fuels and chemicals at room temperature are presented. Specifically, the status and problems of upgrading plastics via electrocatalysis and photoreforming are described, and the photocatalytic oxidation of plastics to chemical feedstocks using oxygen or air as the oxidant is also highlighted. Then, the recent progress in low-temperature thermocatalysis for plastic recycling and upgrading is surveyed. Finally, the challenges and opportunities of catalytic recycling and upgrading of waste plastics under mild conditions are discussed in terms of the catalyst rational design, catalytic system optimization and scalability, and economic feasibility.

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          Production, use, and fate of all plastics ever made

          We present the first ever global account of the production, use, and end-of-life fate of all plastics ever made by humankind.
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            Is Open Access

            Anomalous collapses of Nares Strait ice arches leads to enhanced export of Arctic sea ice

            The ice arches that usually develop at the northern and southern ends of Nares Strait play an important role in modulating the export of Arctic Ocean multi-year sea ice. The Arctic Ocean is evolving towards an ice pack that is younger, thinner, and more mobile and the fate of its multi-year ice is becoming of increasing interest. Here, we use sea ice motion retrievals from Sentinel-1 imagery to report on the recent behavior of these ice arches and the associated ice fluxes. We show that the duration of arch formation has decreased over the past 20 years, while the ice area and volume fluxes along Nares Strait have both increased. These results suggest that a transition is underway towards a state where the formation of these arches will become atypical with a concomitant increase in the export of multi-year ice accelerating the transition towards a younger and thinner Arctic ice pack.
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              Semiconductor-based photocatalytic hydrogen generation.

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                Author and article information

                Contributors
                Journal
                GRCHFJ
                Green Chemistry
                Green Chem.
                Royal Society of Chemistry (RSC)
                1463-9262
                1463-9270
                September 18 2023
                2023
                : 25
                : 18
                : 6949-6970
                Affiliations
                [1 ]Department State Key Laboratory of Chemical Engineering, Department of Chemical Engineering, Tsinghua University, Beijing 100084, China
                [2 ]School of Environmental Science and Engineering, Tianjin Key Laboratory of Biomass/Wastes Utilization, Tianjin University, Tianjin 300350, China
                [3 ]Tianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin, China
                Article
                10.1039/D3GC01872E
                baa1cddd-15ea-4096-a365-d32d7497db63
                © 2023

                http://rsc.li/journals-terms-of-use

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