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Upcycling of monomers derived from waste polyester plastics via electrocatalysis

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Journal of Energy Chemistry 2025年第2期101卷 535-561页

作者： Haoye Wang Richard Lee Smith Jr Xinhua Qi College of environmental Science and engineering Nankai University Graduate school of environmental Studies Tohoku University

Electrocatalysis offers efficient and targeted conversion of monomers derived from waste polyester plastics to chemical products under ambient temperature and pressure *** review provides analysis of research on electrochemical upgrading of monomers derived from waste polyester plastics published from2021 to *** for assessing upgrading of waste polyester plastics include alkaline hydrolysis pretreatment,indices of electrochemical reaction process(activity,stability,and techno-economic a nalysis),separation,and product *** of depolymerization monomers and their value-added products are summarized along with electrocatalytic mechanisms and reaction ***,cathode coupled reactions offer significant value for anodic waste plastic oxidation during electrolysis *** of bifunctional electrocatalysts can reduce the cost of coupled systems and complexity of the *** and recycling of waste plastic monomers using electrocatalytic technology should undergo downstream processing to form high-value products containing C-N and C-S derived functional groups obtained from depolymerized monomers,Electrochemical conversion and upgrading of monomers derived from waste polyester plastics can contribute to industrialization and global economies and help to realize environmental sustainability.

关键词： Coupling reaction Electrocatalysis Monomer Upgrade recycling Value-added products Waste plastics

Charged functional groups modified porous spherical hollow carbon material as CDI electrode for salty water desalination

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Journal of environmental Sciences 2025年第3期149卷 254-267页

作者： Yushan Ni Yunlong Pu Jie Zhang Weiyan Cui Mingjun Gao Dongjiang You school of environmental and Material engineering Yantai UniversityYantai 264005China

As a new electrochemical technology,capacitive deionization(CDI)has been increasingly applied in environmental water treatment and seawater *** this study,functional groups modified porous hollow carbon(HC)were synthesized as CDI electrode material for removing Na^(+)and Cl^(−)in salty *** showed that the average diameter of HC was approximately 180 nm,and the infrared spectrum showed that its surface was successfully modified with sulfonic and amino groups,*** sulfonic acid functionalized HC(HC-S)showed better electrochemical and desalting performance than the amino-functionalized HC(HC–N),with a maximum Faradic capacity of 287.4 F/g and an adsorptive capacity of 112.97 mg/g for ***,92.63%capacity retention after 100 adsorption/desorption cycles demonstrates the excellent stability of *** main findings prove that HC-S is viable as an electrodematerial for desalination by high-performance CDI applications.

关键词： Hollow carbon Functional groups Desalination Capacitive deionization

Anammox-based technologies:A review of recent advances,mechanism,and bottlenecks

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Journal of environmental Sciences 2025年第2期148卷 151-173页

作者： Mabruk Adams Eliasu Issaka Chongjun Chen school of environmental Science and engineering Suzhou University of Science and TechnologySuzhou 2155009China Civil engineering School of EngineeringCollege of Science and EngineeringUniversity of GalwayGalway H91 TK33Ireland school of environmental and Safety engineering Institute of Environmental Health and Ecological SecurityJiangsu UniversityZhenjiang 212013China

The removal of nitrogen via the ANAMMOX process is a promising green wastewater treatment technology,with numerous *** incessant studies on the ANAMMOX process over the years due to its long start-up and high operational cost has positively influenced its technological advancement,even though at a rather slow *** the moment,relatively newANAMMOX technologies are being developedwith the goal of treating lowcarbon wastewater at low temperatures,tackling nitrite and nitrate accumulation and methane utilization from digestates while also recovering resources(phosphorus)in a sustainable *** review compares and contrasts the handful of ANAMMOX-based processes developed thus far with plausible solutions for addressing their respective bottlenecks hindering full-scale ***,future prospects for advancing understanding of mechanisms and engineering application of ANAMMOX process are *** a whole,technological advances in process design and patents have greatly contributed to better understanding of the ANAMMOX process,which has greatly aided in the optimization and industrialization of the ANAMMOX *** review is intended to provide researchers with an overview of the present state of research and technological development of the ANAMMOX process,thus serving as a guide for realizing energy autarkic future practical applications.

关键词： Anammox Commamox Denitrification Full-scale Partial nitrification

A binary eutectic electrolyte design for high-temperature interface-compatible Zn-ion batteries

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Journal of Energy Chemistry 2025年第2期101卷 587-597页

作者： Guomin Li Wentao Wen Kefeng Ouyang Yanyi Wang Jianhui Zhu Ming Yang Hongwei Mi Ning Zhao Peixin Zhang Dingtao Ma College of Chemistry and environmental engineering Shenzhen University school of Materials Science and engineering Harbin Institute of Technology (Shenzhen) school of Materials and environmental engineering Shenzhen Polytechnic Guangdong Flexible Wearable Energy and Tools engineering Technology Research Center

The deterioration of aqueous zinc-ion batteries（AZIBs） is confronted with challenges such as unregulated Zn2+diffusion,dendrite growth and severe decay in battery performance under harsh ***,a design concept of eutectic electrolyte is presented by mixing long chain polymer molecules,polyethylene glycol dimethyl ether（PEGDME）,with H2O based on zinc trifluoromethyl sulfonate(Zn（OTf）2),to reconstruct the Zn2+solvated structure and in situ modified the adsorption layer on Zn electrode *** dynamics simulations（MD）,density functional theory（DFT） calculations were combined with experiment to prove that the long-chain polymer-PEGDME could effectively reduce side reactions,change the solvation structure of the electrolyte and priority absorbed on Zn（002）,achieving a stable dendrite-free Zn *** to the comprehensive regulation of solvation structure and zinc deposition by PEGDME,it can stably cycle for over 3200 h at room temperature at 0.5 mA/cm2and 0.5 mAh/*** at high-temperature environments of 60℃,it can steadily work for more than 800 cycles（1600 h）.Improved cyclic stability and rate performance of aqueous Zn‖VO2batteries in modified electrolyte were also achieved at both room and high *** that,the demonstration of stable and high-capacity Zn‖VO2pouch cells also implies its practical application.

关键词： Dendrite suppression Eutectic electrolyte High temperature Solvation structure Zn anode

Effect of chlorination and ultraviolet on the adsorption of pefloxacin on polystyrene and polyvinyl chloride

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Journal of environmental Sciences 2025年第3期149卷 21-34页

作者： Yanan Li Yaning Wu Kai Guo Weiqin Wu Meijing Yao school of environmental Science and engineering Taiyuan University of TechnologyShanxi 030600China

During thewater treatment process,chlorination and ultraviolet(UV)sterilization can modify microplastics(MPs)and alter their physicochemical properties,causing various changes between MPs and other *** this study,the impact of chlorination and UV modification on the physicochemical properties of polystyrene(PS)and polyvinyl chloride(PVC)were investigated,and the adsorption behavior of pefloxacin(PEF)before and after modificationwas *** effect of pH,ionic strength,dissolved organicmatter,heavymetal ions and other water environmental conditions on adsorption behavior was *** results showed that PS had a higher adsorption capacity of PEF than PVC,and the modification increased the presence of O-containing functional groups in the MPs,thereby enhancing the adsorption capacity of both *** had a more significant impact on the physicochemical properties of MPs compared to UV irradiation within the same time period,leading to better adsorption performance of *** optimal pH for adsorption was found to be 6,and NaCl,sodium alginate and Cu2+would inhibit adsorption to varying degrees,among which the inhibition caused by pH was the *** and UV modification would weaken the inhibitory effect of environmental factors on the adsorption of PEF by *** main mechanisms of adsorption involved electrostatic interaction and hydrogen *** study clarified the effects of modification on the physicochemical properties of MPs,providing reference for subsequent biotoxicity analysis and environmental protection studies.

关键词： Microplastics Chlorination Ultraviolet Pefloxacin Adsorption mechanism

Oxygen atmosphere enhances ball milling remediation of petroleum-contaminated soil and reuse as adsorptive/catalytic materials for wastewater treatment

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Journal of environmental Sciences 2025年第1期147卷 652-664页

作者： Pingting Gao Simin Song Mingxin Wang Meng Yao Jinjuan Xue school of environmental Science and engineering Changzhou UniversityChangzhou 213164China Jiangsu Petrochemical Safety and environmental Protection engineering Research Center Changzhou 213164China

Ball milling is an environmentally friendly technology for the remediation of petroleumcontaminated soil(PCS),but the cleanup of organic pollutants requires a long time,and the post-remediation soil needs an economically viable disposal/reuse strategy due to its vast *** present paper develops a ball milling process under oxygen atmosphere to enhance PCS remediation and reuse the obtained carbonized soil(BCS-O)as wastewater treatment *** total petroleum hydrocarbon removal rates by ball milling under vacuum,air,and oxygen atmospheres are 39.83%,55.21%,and 93.84%,*** Langmuir and pseudo second-order models satisfactorily describe the adsorption capacity and behavior of BCS-O for transition *** Cu^(2+),Ni^(2+),and Mn^(2+)adsorbed onto BCS-O were mainly bound to metal carbonates and metal ***,BCS-O can effectively activate persulfate(PDS)oxidation to degrade aniline,while BCS-O loaded with transition metal(BCS-O-Me)shows better activation efficiency and ***-O and BCS-O-Me activated PDS oxidation systems are dominated by^(1)O_(2)oxidation and electron *** main active sites are oxygen-containing functional groups,vacancy defects,and graphitized *** oxygen-containing functional groups and vacancy defects primarily activate PDS to generate^(1)O_(2)and attack *** carbon promotes aniline degradation by accelerating electron *** paper develops an innovative strategy to simultaneously realize efficient remediation of PCS and sequential reuse of the postremediation soil.

关键词： Petroleum-contaminated soil Ball milling Oxygen atmosphere Pyrolysis Resource utilization

Co-doped cryptomelane-type manganese oxide in situ grown on a nickel foam substrate for high humidity ozone decomposition

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Journal of environmental Sciences 2025年第2期148卷 529-540页

作者： Haoyuan Liang Xu Wang Hui Wang Zhenping Qu Key Laboratory of Industrial Ecology and environmental engineering School of Environmental Science and TechnologyDalian University of TechnologyDalian 116024China

Monolithic catalysts with excellent O_(3)catalytic decomposition performance were prepared by in situ loading of Co-doped KMn_(8)O_(16)on the surface of nickel *** triple-layer structure with Co-doped KMn_(8)O_(16)/Ni6MnO_(8)/Ni foam was grown spontaneously on the surface of nickel foam by tuning the molar ratio of KMnO_(4)to Co(NO_(3))_(2)·6H_(2)O ***,the formed Ni6MnO_(8)structure between KMn_(8)O_(16)and nickel foam during in situ synthesis process effectively protected nickel foam from further etching,which significantly enhanced the reaction stability of *** optimum amount of Co doping in KMn_(8)O_(16)was available when the molar ratio of Mn to Co species in the precursor solution was 2:*** the Mn2Co1 catalyst had abundant oxygen vacancies and excellent hydrophobicity,thus creating outstanding O_(3)decomposition *** O_(3)conversion under dry conditions and relative humidity of 65%,90%over a period of 5 hr was 100%,94%and 80%with the space velocity of 28,000 hr^(−1),*** in situ constructed Co-doped KMn_(8)O_(16)/Ni foam catalyst showed the advantages of low price and gradual applicability of the preparation process,which provided an opportunity for the design of monolithic catalyst for O_(3)catalytic decomposition.

关键词： Co-doped cryptomelane-type manganese O3 decomposition High humidity Nickel foam Monolithic catalyst

Relative humidity-dependent evolution of molecular composition ofα-pinene secondary organic aerosol upon heterogeneous oxidation by hydroxyl radicals

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Journal of environmental Sciences 2025年第2期148卷 210-220页

作者： Wei Wang Chenxi Li Huayun Xiao Ziyue Li Yue Zhao school of environmental Science and engineering Shanghai Jiao Tong UniversityShanghai 200240China

Heterogeneous oxidation by gas-phase oxidants is an important chemical transformation pathway of secondary organic aerosol(SOA)and plays an important role in controlling the abundance,properties,as well as climate and health impacts of ***,our knowledge on this heterogeneous chemistry remains *** this study,the heterogeneous oxidation ofα-pinene ozonolysis SOA by hydroxyl(OH)radicals was investigated under both low and high relative humidity(RH)conditions,with an emphasis on the evolution of molecular composition of SOA and its RH *** is found that the heterogeneous oxidation of SOA at an OH exposure level equivalent to 12 hr of atmospheric aging leads to particle mass loss of 60%at 25%RH and 95%at 90%*** heterogeneous oxidation strongly changes the molecular composition of *** dimer-to-monomer signal ratios increase dramatically with rising OH exposure,in particular under high RH conditions,suggesting that aerosol water stimulates the reaction of monomers with OH radicals more than that of *** addition,the typical SOA tracer compounds such as pinic acid,pinonic acid,hydroxy pinonic acid and dimer esters(e.g.,C17H26O8 and C19H28O7)have lifetimes of several hours against heterogeneous OH oxidation under typical atmospheric conditions,which highlights the need for the consideration of their heterogeneous loss in the estimation of monoterpene SOA concentrations using tracer-based *** study sheds lights on the heterogeneous oxidation chemistry ofmonoterpene SOA andwould help to understand their evolution and impacts in the atmosphere.

关键词： Secondary organic aerosol(SOA) Heterogeneous oxidation Chemical transformation Molecular composition Aerosol water

Integrating Cu+/Cu0 sites on porous nitrogen-doped carbon nanofibers for stable and efficient CO2 electroreduction to multicarbon products

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Journal of Energy Chemistry 2025年第2期101卷 453-462页

作者： Yicheng Chao Jiahao Zhang Qinyue Wu Xinfei Fan Xie Quan Yanming Liu Key Laboratory of Industrial Ecology and environmental engineering (MOE) School of Environmental Science and Technology Dalian University of Technology College of environmental Science and engineering Dalian Maritime University Frontier Science Center for Smart Materials Dalian University of Technology

The Cu+/Cu0sites of copper-based catalysts are crucial for enhancing the production of multicarbon(C2+)products from electrochemical CO2reduction reaction（eCO2RR）.However,the unstable Cu+and insufficient Cu+/Cu0active sites lead to their limited selectivity and stability for C2+***,we embedded copper oxide（CuOx） particles into porous nitrogen-doped carbon nanofibers（CuOx@PCNF）by pyrolysis of the electrospun fiber film containing ZIF-8 and Cu2O *** porous nitrogendoped carbon nanofibers protected and dispersed Cu+species,and its micro porous structure enhanced the interaction between CuOxand reactants during *** obtained CuOx@PCNF created more effective and stable Cu+/Cu0active *** showed a high Faradaic efficiency of 62.5% for C2+products in Hcell,which was 2 times higher than that of bare CuOx（～31.1%）.Furthermore,it achieved a maximum Faradaic efficiency of 80.7% for C2+products in flow *** situ characterization and density functional theory（DFT） calculation confirmed that the N-doped carbon layer protected Cu+from electrochemical reduction and lowered the energy barrier for the dimerization of**** and exposed Cu+/Cu0active sites enhanced the enrichment of*CO and promoted the C-C coupling reaction on the catalyst surface,which facilitated the formation of C2+products.

关键词： Carbon nanofibers Cu+/Cu0 sites C–C coupling Electrocatalytic CO2 reduction Multicarbon products