SinoGreenTech Academic Portal
📚 Peer-Reviewed Translated Literature

All Clean Energy & Battery Intelligence (Page 21)

Browse complete peer-reviewed translations from top indexed Chinese clean energy & battery intelligence journals. Read verified previews and download authentic research reports verified by SinoGreenTech.

Published Research Papers

Showing 24 of 1398 peer-reviewed translated articles (Page 21 of 59)

Combined Effects of Biochar and Riboflavin on the Reduction of Hexavalent Chromium by Shewanella oneidensis MR-1Graphical AbstractVerified
Environmental Chemistry2026

Combined Effects of Biochar and Riboflavin on the Reduction of Hexavalent Chromium by Shewanella oneidensis MR-1

The biological reduction of Cr(VI) to less hazardous Cr(III) is a promising strategy for remediating Cr(VI)-contaminated sites. Both biochar and riboflavin can act as electron shuttles to accelerate this bioreduction process, yet their combined effects remain poorly understood. Using Shewanella oneidensis MR-1 as a model reducing bacterium, we investigated the joint influence of biochar (average particle size 28.85 μm) and riboflavin at high (1 mmol·L−1) and low concentrations on Cr(VI) bioreduction. Individually, biochar and high-concentration riboflavin enhanced indirect electron transfer, accelerating Cr(VI) removal. However, when combined, the fast-phase reaction rate (rf0) did not significantly improve compared to single amendments. The combined action factor revealed an antagonistic inhibition between biochar and riboflavin. Mechanistically, high-concentration riboflavin saturated biochar's adsorption sites (equilibrium concentration 0.96±0.04 mmol·L−1), hindering biochar's role as an electron conduit. With a bacterial density of 3.4×10^7 cells·mL−1, the inter-bacterial distance (30.87 μm) exceeded biochar's particle size, and the per-cell riboflavin concentration (2.9×10−2 pmol·cell−1) was sufficient for riboflavin to dominate as the primary electron shuttle, while biochar's surface became coated, reducing its efficacy. These findings reveal the complex interplay between biochar and soluble organic matter in Cr(VI) bioreduction, underscoring the need to consider such antagonistic effects when designing bioremediation strategies for multi-component contaminated environments.

Read Full Abstract10.7524/j.issn.0254-6108.2024112101
Research Progress on Potassium Permanganate Activated by Carbon Materials for Degradation of Organic PollutantsGraphical AbstractVerified
Environmental Chemistry2026

Research Progress on Potassium Permanganate Activated by Carbon Materials for Degradation of Organic Pollutants

Potassium permanganate (KMnO4) oxidation is a promising technology for organic pollutant removal in water due to its low cost and broad pH applicability. However, its moderate oxidation capacity results in slow degradation rates for refractory organic compounds. Carbon materials (CMs), known for their accessibility, stability, and environmental compatibility, have shown great potential in enhancing KMnO4 oxidation. This paper provides a comprehensive review of recent advancements on the enhancement of KMnO4 oxidation of organic pollutants by CMs. The performance and suitability of various CMs in improving KMnO4 oxidation were systematically compared. Additionally, two key mechanisms driving the degradation of organic pollutants in the KMnO4/CMs system were elucidated, along with a discussion on the recycling and regeneration of CMs. Finally, future research directions and development trends for this technology were outlined, aiming to offer insights to advance the practical application of KMnO4/CMs system in water treatment.

Read Full Abstract10.7524/j.issn.0254-6108.2024120203
Characteristics and Source Apportionment of Water-Soluble Ions in PM2.5 in Taiyuan during Autumn and Winter 2023Graphical AbstractVerified
Environmental Chemistry2026

Characteristics and Source Apportionment of Water-Soluble Ions in PM2.5 in Taiyuan during Autumn and Winter 2023

To investigate the pollution characteristics and temporal variations of water-soluble ions in atmospheric fine particulate matter (PM2.5) during autumn and winter in Taiyuan City, continuous sampling and analysis were conducted using a Swiss Metrohm ion chromatograph in autumn and winter 2023. The results show that the daily mean concentration of nine water-soluble ions was 26.04 μg m−3, accounting for 52.1% of the average PM2.5 mass concentration. Ion concentrations ranked in descending order: NO3−, NH4+, SO42−, Cl−, K+, Na+, Ca2+, F−, and Mg2+. Secondary inorganic ions (SNA) constituted 87.6% of total water-soluble ions. The mass ratio of NO3− to SO42− reached 1.83, indicating a shift from sulfate-dominated to nitrate-dominated aerosol chemistry. During pollution episodes, water-soluble ion concentrations increased exponentially, with distinct ion-specific trends: on moderately polluted days, SO42− increased to 5.31 times that on clean days, whereas on heavily polluted days, NO3− increased to 5.37 times, highlighting nitrate as a primary driver of severe pollution. Comparison with historical data reveals a recent increase in the proportion of water-soluble ions in PM2.5, with higher proportions during more polluted periods. Analysis of NH4+ forms and PM2.5 acidity suggests that acidic components contribute more under heavier pollution. Positive matrix factorization (PMF) identified four major sources: secondary sources, combustion and motor vehicles, industrial sources, and dust. The secondary source contributions were 45.4%, 64.7%, and 63.4% on clean, lightly polluted, and moderate-to-heavy polluted days, respectively, indicating a significantly higher secondary contribution on polluted days.

Read Full Abstract10.7524/j.issn.0254-6108.2025062404
Excitation of Triplet State Dissolved Organic Matter Sensitizes Formic Acid to Generate CO2•− and Its Reductive Degradation of MetronidazoleGraphical AbstractVerified
Environmental Chemistry2026

Excitation of Triplet State Dissolved Organic Matter Sensitizes Formic Acid to Generate CO2•− and Its Reductive Degradation of Metronidazole

Surface waters contain numerous photoactive substances and low molecular weight carboxylic acids (LCAs). Hydroxyl radicals (HO•) can react with LCAs to generate the highly reducing carbon dioxide anion radical (CO2•−). Excited triplet state dissolved organic matter (3DOM*), a common oxidant in surface waters, may also oxidize LCAs to CO2•−, but this pathway remains unexplored. This study simulated sunlight-driven generation of CO2•− via 3DOM* using 4-benzoylbenzoic acid (CBBP) as a 3DOM* precursor and formate (HCOO−) as a model LCA. Metronidazole (MNZ) served as the target pollutant. Comparative degradation experiments in hν, hν/HCOO−, hν/CBBP, and hν/CBBP/HCOO− systems, combined with electron spin resonance spectroscopy and quenching tests, confirmed that CO2•− generated in the hν/CBBP/HCOO− system was the primary reactive species responsible for enhanced MNZ degradation, originating mainly from 3CBBP* oxidizing HCOO−. Under optimized conditions (8 mmol·L−1 HCOO−, 200 μmol·L−1 CBBP, 10 μmol·L−1 MNZ), 98.2% degradation was achieved within 30 min. Degradation efficiency increased with HCOO− concentration and was pH-independent. Cl−, NO3−, CO3^2−, and low concentrations of HCO3− inhibited degradation, while high HCO3− slightly promoted it. Humic acid (HA) inhibited degradation in a concentration-dependent manner. The system also performed well in real water matrices, suggesting potential for treating micropollutants via reductive pathways.

Read Full Abstract10.7524/j.issn.0254-6108.2024120701
Research Progress in Metal Stable Isotope Fractionation in Coal-Fired BoilersGraphical AbstractVerified
Environmental Chemistry2026

Research Progress in Metal Stable Isotope Fractionation in Coal-Fired Boilers

Coal-fired boilers are significant anthropogenic sources of metal emissions, contributing over half of certain toxic heavy metal releases. Metal stable isotopes have been widely applied to trace metal pollutants from coal-fired power plants and other sources. However, complex physicochemical processes within boilers induce isotopic fractionation between raw coal and combustion products, complicating source tracing. This review outlines the structure and operational principles of coal-fired boiler systems, focusing on recent advancements in understanding the isotopic fractionation behavior of mercury (Hg), zinc (Zn), cadmium (Cd), and lead (Pb) during coal combustion and flue gas emission. These elements exhibit distinct fractionation patterns due to volatility and condensation dynamics. For instance, Hg, being highly volatile, undergoes significant mass-dependent and mass-independent fractionation, while semi-volatile elements like Cd and Zn show enrichment in fine fly ash. The review emphasizes the necessity of characterizing boiler-specific fractionation factors to improve the accuracy of isotopic tracing. It synthesizes field measurements and laboratory studies, highlighting that fractionation magnitudes can exceed analytical uncertainties by tens of times. The paper also discusses the influence of air pollution control devices (APCDs) such as selective catalytic reduction (SCR) and electrostatic precipitators (ESP) on isotope signatures. Ultimately, this work provides a framework for using metal isotopes as robust tracers in environmental forensics, underscoring the need for comprehensive understanding of boiler processes to interpret isotopic data correctly.

Read Full Abstract10.7524/j.issn.0254-6108.2024112103
Emission Inventory and Scenario Prediction of Non-Road Mobile Sources in Hebei ProvinceGraphical AbstractVerified
Environmental Chemistry2026

Emission Inventory and Scenario Prediction of Non-Road Mobile Sources in Hebei Province

Based on the 2022 activity data of non-road mobile sources in Hebei Province, this study employed the emission factor method recommended by the Guidelines to estimate emissions of CO, HC, NOx, PM2.5, PM10, and SO2. A comprehensive emission inventory was established, followed by spatial and uncertainty analyses. Scenario analysis, aligned with the 14th Five-Year Plan policies, was used to project emissions for 2030. The results indicate that non-road mobile sources in Hebei emitted 76.1×10^3 t of CO, 20.6×10^3 t of HC, 164.0×10^3 t of NOx, 8.5×10^3 t of PM2.5, 9.0×10^3 t of PM10, and 2.4×10^3 t of SO2. Agricultural machinery was the dominant contributor to CO, HC, PM2.5, and PM10, accounting for over 60.0% of CO emissions. Railway locomotives were the primary source of NOx, contributing 50.9%. For SO2, agricultural machinery and railway locomotives contributed 39.0% and 44.4%, respectively. The highest emitting cities were Tangshan (21.3%), Shijiazhuang (15.7%), Cangzhou (11.6%), and Handan (11.6%). Ship emissions were concentrated in Tangshan Port; civil aviation emissions were mainly in Shijiazhuang, Tangshan, Qinhuangdao, and Handan; railway emissions were distributed in Shijiazhuang, Baoding, and Handan. Under the updated emission standard scenario, NOx and PM10 emissions in 2030 could be reduced by approximately 35.0%. The phase-out of old machinery yielded the largest reduction in CO (36.0%), while both electrification and phase-out scenarios significantly impacted HC emissions.

Read Full Abstract10.7524/j.issn.0254-6108.2024112102
Effect of Water Vapor and Nitrogen Oxides on Electricity Pulse-Sparked Catalysis for Soot CombustionGraphical AbstractVerified
Environmental Chemistry2026

Effect of Water Vapor and Nitrogen Oxides on Electricity Pulse-Sparked Catalysis for Soot Combustion

The rapid combustion of soot at low temperatures is critical for diesel engine cold-start emission control. This study investigates the effects of water vapor (H2O) and nitrogen oxides (NOx) on electricity-pulse-sparked catalysis (EPSC) for soot combustion over a ceramic filter paper-based potassium-supported antimony-doped tin oxide (K/ATO/CP) monolithic catalyst. Under EPSC with 2000 J pulses, the presence of H2O and NOx adversely affected soot combustion performance, yet average reaction rates remained high at 12.0 μmol·gcat−1·s−1 and 9.53 μmol·gcat−1·s−1, respectively, exceeding conventional thermal catalysis (<8 μmol·gcat−1·s−1). In situ Raman and concentration profiles revealed that electricity pulses promote rapid H2O desorption, effectively alleviating H2O poisoning and restoring catalyst activity. In contrast, NOx adsorption forms stable nitrates (e.g., KNO3) that desorb slower than the soot combustion process, leading to incomplete recovery of activity. These findings highlight the importance of adsorbate desorption kinetics in EPSC and suggest that using weakly basic alkaline-earth metals (e.g., Mg, Ca, Sr) with lower nitrate decomposition temperatures could mitigate NOx poisoning. The results provide guidance for advancing EPSC technology in hybrid vehicle exhaust aftertreatment systems.

Read Full Abstract10.7524/j.issn.0254-6108.2024102403
Effect of Fullerene C60 on Sulfate Formation during Gas-Phase Oxidation of SO2 by H2O2Graphical AbstractVerified
Environmental Chemistry2026

Effect of Fullerene C60 on Sulfate Formation during Gas-Phase Oxidation of SO2 by H2O2

Fullerene (C60) is an emerging atmospheric pollutant that may influence sulfate formation during haze events. This study investigated the effect of C60 on sulfate production in the gas-phase oxidation of SO2 by H2O2 using a flow tube reactor. Results demonstrated that the presence of C60 significantly increased sulfate yields. Control experiments varying C60 loading, H2O2 concentration, and ultraviolet (UV) irradiation revealed that higher C60 amounts, elevated H2O2 levels, and UV exposure enhanced the promoting effect. Mechanistic investigations via free radical trapping and X-ray photoelectron spectroscopy (XPS) indicated a pre-adsorption-oxidation pathway. XPS analysis showed electron transfer on the C60 surface, converting adsorbed S(IV) to S(VI), confirming direct participation of C60 in sulfate formation. Radical trapping experiments and model calculations confirmed that C60 promotes the generation of hydroxyl radicals (·OH) and superoxide radicals (·O2−), which are key oxidants driving SO2 conversion to sulfate. The study reveals that C60 particles markedly enhance atmospheric sulfate formation, offering a novel pathway for understanding sulfate generation mechanisms. These findings have implications for air quality modeling and haze mitigation strategies, as C60 may act as a catalytic surface for sulfate production in polluted atmospheres.

Read Full Abstract10.7524/j.issn.0254-6108.2024122501
Induced Exposure Strategy to Achieve Synergistic Catalytic Elimination of CH3SH and CO2 by Al2O3Graphical AbstractVerified
Environmental Chemistry2026

Induced Exposure Strategy to Achieve Synergistic Catalytic Elimination of CH3SH and CO2 by Al2O3

Selective synergistic catalytic elimination (SSCE) of CH3SH and CO2 represents a significant approach towards achieving green chemistry objectives. In this study, a series of Al2O3 catalysts with different surface hydroxyl coordination states were designed and fabricated through a simple water bath strategy. The performance of the corresponding catalysts for selective synergistic catalytic elimination of CH3SH and CO2 was systematically evaluated. The catalysts were comprehensively characterized by BET, XRD, XPS, NMR and CO-DRIFTS techniques. The experimental results revealed that the synthesized samples exhibited uniform specific surface areas (150 m2·g−1) and pore sizes (12 nm), while demonstrating varying hydroxyl coordination states, which significantly affects the surface acidity of W-Al2O3 catalyst. Notably, W80-Al2O3, synthesized at 80 °C via water bath heating, displayed the highest proportion of μ1-type hydroxyl coordination. This unique structural feature endowed the catalyst with enhanced Brønsted acidity and superior CO adsorption capacity compared to other catalysts, which significantly promotes the further hydrogenation of CO to CH4 in the SSCE process. As a result, the SSCE performance of W80-Al2O3 was significantly improved, achieving complete conversion of CH3SH (100%) and a CH4 product concentration of 1326 μmol·g−1, which is significantly higher than that of Al2O3 (56 μmol·g−1) and W-Al2O3 (54 μmol·g−1). This work provides a new strategy for the synergistic reduction of typical sulfur-containing odorous pollutants and carbon dioxide.

Read Full Abstract10.7524/j.issn.0254-6108.2024112106
Covalent Modification of MIL-101 for Enhanced Tetracycline Adsorption from Aqueous SolutionsGraphical AbstractVerified
Environmental Chemistry2026

Covalent Modification of MIL-101 for Enhanced Tetracycline Adsorption from Aqueous Solutions

The pervasive presence of tetracycline (TC) in aquatic environments poses significant ecological and public health risks. This study reports the synthesis of MIL-101-Bim, a covalently modified metal-organic framework (MOF), via a pre-modification strategy that introduces formyl groups into the MIL-101(Cr) framework (MIL-101-CHO), followed by Schiff base condensation and NaBH4 reduction to graft benzimidazole moieties. Powder X-ray diffraction (PXRD) and scanning electron microscopy (SEM) confirmed retention of the parent MIL-101(Cr) topology. Fourier-transform infrared (FT-IR) spectroscopy verified successful functionalization. 1H NMR analysis of digested MIL-101-Bim revealed a benzimidazole modification degree of 41%, with 32% of formyl groups reduced to hydroxymethyl and 27% remaining unreacted. Thermogravimetric analysis (TGA) demonstrated good thermal stability. Nitrogen adsorption-desorption measurements showed a specific surface area of 1361 m2·g−1 and pore sizes ranging from 1 to 2.3 nm. Adsorption kinetics for TC on both materials followed a pseudo-second-order model, and isotherm data fitted the Langmuir model. The theoretical maximum adsorption capacity of MIL-101-Bim for TC was 86.31 mg·g−1, significantly higher than that of MIL-101-CHO (39.56 mg·g−1). Zeta potential measurements indicated optimal adsorption performance at pH 5–8. X-ray photoelectron spectroscopy (XPS) provided evidence of hydrogen bond formation during adsorption. The adsorption mechanism involves both physical adsorption (pore filling, electrostatic interactions, π-π stacking) and chemical adsorption (weak hydrogen bonding). Regeneration studies showed that MIL-101-Bim retained an adsorption capacity of 46.93 mg·g−1 after five cycles, demonstrating promising reusability.

Read Full Abstract10.7524/j.issn.0254-6108.2025112601
Bismuth Upconversion Luminescent Glass for Fluoride Removal and Photocatalytic Performance of the Fluoride Removal ProductsGraphical AbstractVerified
Environmental Chemistry2026

Bismuth Upconversion Luminescent Glass for Fluoride Removal and Photocatalytic Performance of the Fluoride Removal Products

Fluoride-containing wastewater treatment typically relies on calcium-based precipitation and flocculation, which suffer from low compliance rates and difficult valorization of fluoride-laden sludge. This study introduces a novel bismuth upconversion luminescent glass (BULG) synthesized from Bi2O3, SiO2, Yb2O3, and Er2O3, designed for efficient fluoride removal and subsequent photocatalytic application. By varying the Bi2O3:SiO2 molar ratio, a series of BULGs with superior upconversion luminescence were obtained. Under optimal conditions (Bi3+:F− molar ratio = 1:1, pH = 2), fluoride removal efficiencies exceeded 97% for all compositions, with the 0.7:0.3 Bi2O3:SiO2 formulation achieving 99.9% removal and rapid settling of the precipitate. The fluoride removal products retained upconversion luminescence and exhibited semiconductor heterojunctions, enabling complete photocatalytic degradation of ciprofloxacin (100% within 60 min). This approach not only efficiently removes fluoride ions but also valorizes the waste into a functional photocatalyst, offering a promising strategy for fluoride-containing wastewater treatment.

Read Full Abstract10.7524/j.issn.0254-6108.2024102303
Synergistic Regulation by Long- and Short-Chain Quorum Sensing Signaling Molecules Enhances Sulfamethoxazole Metabolism in Electroactive Biofilms within a Microbial Electrolysis Cell Coupled Anaerobic Digestion SystemGraphical AbstractVerified
Journal of Environmental Engineering Technology2026

Synergistic Regulation by Long- and Short-Chain Quorum Sensing Signaling Molecules Enhances Sulfamethoxazole Metabolism in Electroactive Biofilms within a Microbial Electrolysis Cell Coupled Anaerobic Digestion System

High-strength sulfamethoxazole (SMX) wastewater severely inhibits anaerobic microorganisms, reducing organic degradation and methane yield. This study investigated the effects of short-chain (C6-HSL) and long-chain (C12-HSL) N-acyl-homoserine lactone (AHL) signaling molecules, individually and in combination, on the construction, performance, and antibiotic resistance gene (ARG) profiles of anaerobic electroactive biofilms within a microbial electrolysis cell coupled anaerobic digestion (MEC-AD) system. Compared to the control (no AHLs), SMX removal efficiency increased by 9.26%, 7.44%, and 10.67% for C6-HSL (T1), C12-HSL (T2), and combined (T3) treatments, respectively. Methane production rates rose by 20.4%, 16.9%, and 23.1% for T1, T2, and T3, respectively. AHLs promoted extracellular polymeric substance secretion, enhancing electroactive microbe attachment to the anode. Microbial community analysis revealed increased diversity and modulated key functional genera. Notably, Georgenia abundance increased by 16.77% (T1) and 36.47% (T3) but decreased by 15.99% (T2). ARG analysis showed that single AHLs elevated intI1, sul1, and sul2 abundances, whereas combined AHLs (T3) exhibited a milder response, with sul2 abundance reduced by 4.92% relative to control. This suggests synergistic AHLs suppress ARG host proliferation. This study first demonstrates that combined short- and long-chain AHLs enhance electroactive biofilm formation, maintain microbial community stability, and modulate ARG dissemination risk, offering a quorum sensing-based strategy for antibiotic wastewater treatment and risk management.

Read Full Abstract10.13205/j.hjgc.202604006
Preparation of Solid-Phase Carbon Sources with Different Ratios and Their Carbon Release PropertiesGraphical AbstractVerified
Journal of Environmental Engineering Technology2026

Preparation of Solid-Phase Carbon Sources with Different Ratios and Their Carbon Release Properties

Low C/N ratios in wastewater treatment plant effluent necessitate external carbon sources for denitrification, but conventional liquid carbon sources are costly and unstable. This study prepared nine composite solid-phase carbon sources by combining PHBV with natural cellulose materials (straw, sawdust, corncob) at different mass ratios. Dynamic release experiments, DOC analysis, UV-Vis spectroscopy, and EEM fluorescence were employed to characterize carbon release. Results showed that increasing cellulose proportion in corncob-based sources led to release patterns opposite to those of straw- and sawdust-based sources. For straw and sawdust, higher cellulose ratios accelerated release rates, increased total release and duration, reduced aromaticity and molecular weight of released DOM, and promoted protein-like components (tryptophan, tyrosine), indicating enhanced bioavailability. Under identical ratios, corncob-based sources exhibited moderate total release, release durations exceeding 134 h, lower DOM aromaticity and molecular weight, and lower humic substance proportion, indicating superior bioavailability and engineering potential. Among the nine sources, JG5, MX5, and CC4 (PHBV:cellulose mass ratios of 4:5, 4:5, and 1:1, respectively) showed optimal comprehensive performance with low theoretical maximum release, long release periods, and high mass transfer coefficients. EEM-PARAFAC identified three DOM components (protein-like C1, C2; humic-like C3), with protein-like components dominating. This study validates the relationship between cellulose proportion and release kinetics and reveals synergistic regulation of DOM components, offering guidance for designing effective solid-phase carbon sources.

Read Full Abstract10.13205/j.hjgc.202604007
Enhancement of Anaerobic Digestion Operational Efficiency for Guar Gum Production Wastewater Using a Microaerobic-Biochar Coupled SystemGraphical AbstractVerified
Journal of Environmental Engineering Technology2026

Enhancement of Anaerobic Digestion Operational Efficiency for Guar Gum Production Wastewater Using a Microaerobic-Biochar Coupled System

Guar gum production wastewater contains 1,2-propanediol, which in conventional anaerobic treatment causes propionate accumulation and microbial inhibition. Microaerobic conditions foster fermentative bacterial metabolism, enhancing organic substrate conversion, while biochar promotes anaerobic microbial aggregation and oxygen tolerance. This study treated actual guar gum wastewater using three configurations: blank control, anaerobic, and microaerobic-biochar (O2/BC) coupled systems. Under mesophilic conditions (37 °C), with micro-aeration at 0.2 mL/(g VS·d) and biochar dosage of 15 g/L, the O2/BC system achieved a COD removal efficiency of 90%, 10.6 percentage points higher than the anaerobic control. Effluent COD and propionate concentrations dropped to 3800 mg/L and 0.15 g/L, respectively, representing reductions of 49.6% and 98.4% versus the control. Biogas production was 1.64 times that of the control, with a maximum methane concentration of 77.2%. Fourier transform infrared spectroscopy (FT-IR) indicated increased abundance of –OH, –CH2–, and C–O functional groups on sludge surfaces, revealing biochar's adsorption enhancement. Scanning electron microscopy (SEM) showed dense microbial aggregates dominated by long bacilli, distinct from conventional anaerobic sludge. Microbial community analysis revealed increased abundance of Clostridium and Comamonas, modulating the propionate-to-acetate ratio and optimizing acidification efficiency, thereby promoting complex organic degradation. This study provides a novel technical pathway for biological treatment of alcohol-rich organic wastewater.

Read Full Abstract10.13205/j.hjgc.202604010
Simultaneous Determination of Eleven Organic Ultraviolet Absorbents in Coral by Ultra-High Performance Liquid Chromatography-Mass SpectrometryGraphical AbstractVerified
Environmental Chemistry2026

Simultaneous Determination of Eleven Organic Ultraviolet Absorbents in Coral by Ultra-High Performance Liquid Chromatography-Mass Spectrometry

An analytical method was developed for the simultaneous determination of 11 organic ultraviolet absorbents (OUVs) in coral tissues using ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS). Target analytes included benzophenones (BP, BP-2, BP-3, BP-8) and other common UV filters. Sample pretreatment and chromatographic conditions were systematically optimized. Coral tissue samples were extracted by combined vortexing and ultrasonication, separated on a CAPCELL PAK MG C18 column using a mobile phase of methanol-0.1% formic acid aqueous solution under gradient elution, and determined by multiple reaction monitoring (MRM) with internal standard quantification. Method validation demonstrated good linearity for all target compounds over the range of 0.1–500 μg·L−1 (R2 > 0.990), with method detection limits ranging from 0.020 to 0.133 ng·g−1. The mean recoveries at low, medium, and high spiking levels ranged from 60.5% to 120.3%, with relative standard deviations (RSDs) of 1.6%–10.7%. The method offers advantages of simple pretreatment, good repeatability, and high accuracy, making it suitable for high-throughput determination of OUVs in complex biological matrices such as corals. The method was applied to analyze 89 coral samples collected from Xidao Island, Sanya, and five target OUVs were detected in the samples. This method provides reliable technical support for elucidating the accumulation characteristics of OUVs in corals and assessing their potential ecological risks.

Read Full Abstract10.0000/202604-1
Occurrence Characteristics, Source Apportionment, and Ecological Risk Assessment of Pesticides in Plateau Lakes: A Case Study of Dianchi LakeGraphical AbstractVerified
Journal of Environmental Engineering Technology2026

Occurrence Characteristics, Source Apportionment, and Ecological Risk Assessment of Pesticides in Plateau Lakes: A Case Study of Dianchi Lake

This study systematically investigated the occurrence, spatial distribution, sources, and ecological risks of 160 pesticides in Dianchi Lake, a typical plateau lake impacted by agricultural activities. A total of 37 pesticides were detected in the water, with total concentrations ranging from 64.2 to 1132.8 ng/L (average 610.0 ng/L). Fungicides, including boscalid (BOS), fluopicolide (FPC), and dimethomorph (DMM), were dominant, contributing up to 65.0% of the total concentration. Spatially, the southern lake region exhibited significantly higher concentrations (672.5 ng/L) than the north, attributed to intensive facility agriculture. Highly hydrophobic pesticides, such as penconazole (PEN), showed a tendency to enrich in bottom layers. Source apportionment identified inflowing rivers and wastewater treatment plant effluents as primary input sources, with average concentrations 7 and 9 times higher than lake water, respectively. Ecological risk assessment revealed that pesticides posed the highest risk to algae, followed by daphnia and fish. Prometryn (PMT) was identified as a high-risk factor for algae, while profenofos (PFF) and carbendazim (CBD) posed potential threats to higher trophic levels. These findings provide fundamental data and technical support for understanding pesticide pollution in plateau lake ecosystems.

Read Full Abstract10.13205/j.hjgc.202604001
Microbiome Mechanisms of Composite Carbon Sources for Enhancing Denitrification and Reducing N2O EmissionsGraphical AbstractVerified
Journal of Environmental Engineering Technology2026

Microbiome Mechanisms of Composite Carbon Sources for Enhancing Denitrification and Reducing N2O Emissions

Biological nitrogen removal in wastewater treatment plants (WWTPs) is often limited by insufficient influent carbon sources, necessitating external carbon addition to enhance denitrification. Conventional single carbon sources, such as sodium acetate, frequently fail to meet the metabolic demands of complex microbial communities, compromising nitrogen removal efficiency and stability. Composite carbon sources, by providing multiple electron donors, can improve metabolic cooperation among microorganisms, yet their underlying microbial mechanisms remain insufficiently understood. In this study, activated sludge from a municipal WWTP was used to investigate the microbial mechanisms of composite carbon sources during denitrification. Batch denitrification experiments were conducted in combination with metagenomic and metatranscriptomic analyses to systematically characterize microbial community structure and functional gene expression under different carbon source conditions. Results showed that, compared with sodium acetate as the single carbon source, the composite carbon source system (sodium acetate: sodium succinate: ethanol = 2:1:3) increased the denitrification rate from (6.822 ± 0.141) mg/(L·h) to (8.370 ± 0.186) mg/(L·h), representing a 22.7% improvement, while reducing N2O accumulation by approximately 55%. Metagenomic analysis revealed that Ottowia, Rubrivivax, Thauera, and Zoogloea were the dominant denitrifying genera. Metatranscriptomic results further demonstrated that the composite carbon sources significantly upregulated the transcription of key denitrification genes, with nirS, norB, and nosZ increasing by 37.8%, 27.4%, and 48.6%, respectively. In addition, the composite carbon sources promoted complementary carbon metabolic strategies among different microbial communities, enhancing electron donor supply and improving denitrification efficiency. These findings indicate that composite carbon sources synergistically enhance denitrification performance through regulation of functional gene transcription in complex microbial communities, providing a theoretical basis for carbon source optimization in WWTPs.

Read Full Abstract10.13205/j.hjgc.202604009
Key Environmental Behaviors and Pollution Control Strategies of Tire Wear Particles in Aquatic EnvironmentsGraphical AbstractVerified
Journal of Environmental Engineering Technology2026

Key Environmental Behaviors and Pollution Control Strategies of Tire Wear Particles in Aquatic Environments

Tire wear particles (TWPs) are emerging pollutants and constitute the dominant type of microplastics (MPs) in urban stormwater runoff, accounting for up to 90% of MPs in some cases. They are characterized by small size, high mobility, complex composition, and significant toxicity. Current research on TWPs remains fragmented, lacking a comprehensive understanding of their environmental behaviors and pollution control in aquatic systems. This review systematically analyzes the enrichment and vectoring roles of TWPs for coexisting pollutants, and their environmental fate, including ecotoxicological impacts, detection methodologies, release of intrinsic additives, and aggregation and sedimentation behaviors. Drawing on insights from other microplastic studies, the paper explores control technologies across the pollution pathway—source, transport, and terminal treatment—and proposes feasible management strategies. Key findings indicate that TWPs can adsorb heavy metals and organic contaminants, with adsorption capacities influenced by aging processes. Their aggregation is governed by solution chemistry, with critical coagulation concentrations varying with ionic strength and pH. The release of additives such as zinc and benzothiazoles is significant, posing ecological risks. Future research should focus on real-water aggregation mechanisms, additive release under natural conditions, long-term performance of treatment facilities like constructed wetlands under TWPs stress, enzymatic degradation pathways, and integration of AI, big data, and IoT for cost-effective detection and risk modeling. This review provides a scientific basis for developing targeted pollution control measures for TWPs in aquatic environments.

Read Full Abstract10.13205/j.hjgc.202604004
Spatial Heterogeneity of Reverse Osmosis Membrane Fouling During Long-Term Reclaimed Water Treatment: A 3.5-Year Field StudyGraphical AbstractVerified
Journal of Environmental Engineering Technology2026

Spatial Heterogeneity of Reverse Osmosis Membrane Fouling During Long-Term Reclaimed Water Treatment: A 3.5-Year Field Study

Reverse osmosis (RO) membrane fouling remains a critical bottleneck in reclaimed water production, yet its spatial heterogeneity over extended operation is poorly understood. This study investigated fouling characteristics and microbial community dynamics on RO membranes after 3.5 years of operation in a full-scale microfiltration-reverse osmosis (MF-RO) system treating reclaimed water. Long-term monitoring showed stable effluent quality (turbidity <0.1 NTU, conductivity <400 μS/cm), but RO inlet pressure exhibited seasonal fluctuations of 15%–22% between summer and winter, attributed to water viscosity changes. Membrane autopsies revealed distinct fouling layers at the inlet (RO1) and outlet (RO2) ends. RO1 featured a dense bio-inorganic composite fouling layer with CaSO4 crystals and rod-shaped microbial aggregates (5–10 μm), dominated by Proteobacteria (77.11%), particularly Alphaproteobacteria (71.49%) and Xanthobacteraceae (35.29%), which secreted extracellular polymeric substances (EPS) to form biofilms. In contrast, RO2, exposed to higher salinity, showed reduced microbial abundance (Proteobacteria decreased to 64.79%) and a shift toward halotolerant taxa, including Microbacteriaceae (23.73%) and Actinobacteriota (24.76%), with EPS secretion increased by 42%. Alphaproteobacteria relative abundance dropped by 19.3%, while Gammaproteobacteria rose to 12.54%. These findings elucidate salinity-driven microbial succession and spatial heterogeneity of fouling, providing a basis for targeted antifouling strategies and 'zonal-graded' cleaning protocols in reclaimed water plants.

Read Full Abstract10.13205/j.hjgc.202604011
Non-targeted Analysis of Emerging Contaminant Characteristics and Distribution Differences in Wastewater from a Metro Maintenance DepotGraphical AbstractVerified
Journal of Environmental Engineering Technology2026

Non-targeted Analysis of Emerging Contaminant Characteristics and Distribution Differences in Wastewater from a Metro Maintenance Depot

Emerging contaminants (ECs) in wastewater from urban transportation infrastructure remain poorly characterized. This study employed high-resolution mass spectrometry (HRMS)-based non-target screening to systematically identify the composition and spatial distribution of ECs in wastewater from three functional zones of a metro maintenance depot: storeroom (S1), office/residential area (S2), and final discharge outlet (S3). A total of 417 contaminants were detected, spanning eight categories including industrial materials, pharmaceuticals, pesticides, and natural products. Among these, 48 substances were identified with Level 1 confidence via spectral matching. Pesticides exhibited the highest detection frequency and concentration levels, representing the primary contaminant load. Semi-quantitative concentration heatmaps of 24 pesticides revealed significant spatial variation: S2 showed the highest number and concentration of contaminants, reflecting inputs from landscaping and vector control; S1 and S3 showed lower levels, indicating dilution, migration, and attenuation. Representative pesticide bifenox displayed a clear concentration gradient (S2 > S1 > S3), suggesting transport mechanisms such as surface runoff, hydraulic transfer, and sorption. These findings underscore the complexity and diversity of EC sources in metro depot wastewater, highlight the need to prioritize pesticides in regulatory management, and provide fundamental data for understanding EC environmental behavior and informing water environment risk assessment.

Read Full Abstract10.13205/j.hjgc.202604003
Effects of Exogenous Antibiotic-Resistant Bacteria Exposure on Wheat Seedling Growth and Its Root Endophytes and Rhizosphere Bacterial CommunitiesGraphical AbstractVerified
Journal of Environmental Engineering Technology2026

Effects of Exogenous Antibiotic-Resistant Bacteria Exposure on Wheat Seedling Growth and Its Root Endophytes and Rhizosphere Bacterial Communities

To elucidate the effects of exogenous antibiotic-resistant bacteria (ARB) exposure on wheat growth and associated bacterial community assembly, the inhibitory impacts of exogenous ARB on wheat seedling root and shoot length, shifts in root endophytic and rhizosphere bacterial communities, and the horizontal transfer of exogenous antibiotic resistance genes (ARGs) to indigenous endophytic bacteria were investigated using plate culture counting and 16S rRNA high-throughput sequencing. The results showed that exogenous ARB exposure significantly suppressed wheat seedling root and shoot growth, with inhibition rates increasing in an ARB concentration-dependent manner. At an exogenous ARB concentration of 108 CFU/mL, the inhibition rates of seedling root and shoot length reached 68.83% and 36.87%, respectively. During the period of ARB exposure, the relative abundance of Clostridium_sensu_stricto_5 in root endophytic bacteria increased rapidly, becoming the most dominant genus (45.02%) by the end of the exposure period. In contrast, Betaproteobacteriales remained the dominant order in the rhizosphere bacterial community throughout the experiment, with its relative abundance increasing continuously over time. The proportion of ARB-carrying endophytic bacteria initially decreased and then increased during exposure, showing a significant positive correlation with the relative abundances of Clostridium_sensu_stricto_5, Clostridium_sensu_stricto_1, Bacillus, and Paenibacillus (P<0.05). In summary, exogenous ARB exposure significantly inhibits wheat seedling growth and alters the community structure of both root endophytic and rhizosphere bacteria. Sustained ARB exposure leads to the transfer of exogenous ARGs to root endophytes, and Clostridium_sensu_stricto species may act as potential hosts for ARGs in wheat seedling roots.

Read Full Abstract10.13205/j.hjgc.202604005
Determination of 22 Per- and Polyfluoroalkyl Substances in Surface Water by Solid-Phase Extraction with Ultra-High Performance Liquid Chromatography-Tandem Mass SpectrometryGraphical AbstractVerified
Journal of Environmental Engineering Technology2026

Determination of 22 Per- and Polyfluoroalkyl Substances in Surface Water by Solid-Phase Extraction with Ultra-High Performance Liquid Chromatography-Tandem Mass Spectrometry

A robust analytical method was developed for the simultaneous determination of 22 per- and polyfluoroalkyl substances (PFAS) in surface water using ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS). To address the loss of particle-bound PFAS, the method incorporates a methanol extraction step for particulate matter retained on filters, followed by combining the extract with the filtrate. Samples were then concentrated and purified using weak anion exchange (WAX) solid-phase extraction (SPE) cartridges. After nitrogen evaporation, the residue was reconstituted in methanol/water (8:2, v/v) and filtered prior to analysis. Quantification was performed using isotope dilution. The method exhibited excellent linearity (R² > 0.995) over a concentration range of 1–250 µg/L. Method detection limits ranged from 0.2 to 0.6 ng/L, and method quantification limits from 0.8 to 2.4 ng/L. Recoveries in blank water and surface water matrices were 85.3%–139% and 76.4%–127%, respectively, with relative standard deviations (RSD, n=6) below 15%. Compared to conventional methods without particulate extraction, this approach significantly improved recovery rates in surface water, effectively eliminating negative bias caused by particle adsorption. The method is sensitive, accurate, and reliable, making it suitable for routine monitoring of PFAS in surface water.

Read Full Abstract10.13205/j.hjgc.202604002
A Pilot-Scale Study on Iron-Driven Autotrophic Denitrification Enhanced by CF-Fe-CS Cathode for Low C/N Wastewater TreatmentGraphical AbstractVerified
Journal of Environmental Engineering Technology2026

A Pilot-Scale Study on Iron-Driven Autotrophic Denitrification Enhanced by CF-Fe-CS Cathode for Low C/N Wastewater Treatment

Municipal wastewater treatment plant (WWTP) effluent in China typically exhibits a low carbon-to-nitrogen (C/N) ratio, necessitating substantial external carbon addition for conventional heterotrophic denitrification, which incurs high costs and secondary pollution risks. Nitrate-dependent ferrous oxidation (NDFO) offers a promising alternative, yet suffers from unsustainable iron sources and surface passivation. This study constructed a pilot-scale electrochemical-biological coupled system (CF-Fe-CS/NAFO) with an effective volume of 200 L and a treatment capacity of 100 L/d, incorporating a composite cathode (5% apparent filling rate of carbon felt-iron-chitosan, CF-Fe-CS). A constant potential of -1.0 V (vs. Ag/AgCl) was applied to the cathode to achieve in-situ electrochemical reduction of Fe(III). During stable operation from day 16 to 60 with a hydraulic retention time (HRT) of 48 h and synthetic influent containing 15 mg/L NO3-N, effluent NO3-N remained below 6.5 mg/L, achieving total nitrogen (TN) removal of 50-60%, whereas the control reactor (no applied potential) exhibited effluent NO3-N above 12 mg/L and TN removal below 20%. From day 61 to 74, treating real secondary sedimentation tank effluent (influent NO3-N: 15.29 mg/L), the system reduced effluent NO3-N to 6.06 mg/L, maintaining TN removal above 50%. From day 74 to 98, as HRT was sequentially reduced from 48 h to 24, 12, 6, and 3 h, effluent NO3-N increased to 9.5, 11.9, 13.6, and 14.6 mg/L, with TN removal efficiencies of 32.6%, 19.9%, 10.9%, and 5.8%, respectively. These results demonstrate that the CF-Fe-CS/NAFO system achieves long-term, stable, advanced nitrogen removal from WWTP secondary effluent without external organic carbon.

Read Full Abstract10.13205/j.hjgc.202604008
Design and Operational Performance of a Modified Bardenpho Process in a Wastewater Treatment PlantGraphical AbstractVerified
Journal of Environmental Engineering Technology2026

Design and Operational Performance of a Modified Bardenpho Process in a Wastewater Treatment Plant

A newly constructed wastewater treatment plant with a design capacity of 100,000 m3/d receives influent containing approximately 15% industrial wastewater, resulting in water quality and quantity fluctuation coefficients of 1.2–1.5, refractory organic matter (as COD) exceeding 35% of total COD, and a total nitrogen (TN) concentration up to 55 mg/L. To ensure stable effluent compliance and enhance shock resistance, a modified Bardenpho process was implemented, integrating multi-point influent distribution, post-anoxic and post-aerobic zones, and supplemented with an equalization basin, high-efficiency sedimentation tank, and denitrifying deep-bed filter. During commissioning and operation, the process achieved average removal efficiencies of 96.10% for COD, 98.24% for NH3-N, 83.89% for TN, and 98.29% for TP. Effluent concentrations stabilized at 15.4 mg/L COD, 0.57 mg/L NH3-N, 7.94 mg/L TN, and 0.12 mg/L TP, consistently meeting the Class 1A standard of GB 18918—2002. The modified Bardenpho process demonstrates strong adaptability and stability for treating wastewater with high nitrogen and refractory organic loads, improving carbon source utilization and reducing energy consumption. Design parameters and operational experience provide valuable references for similar municipal plants, particularly those receiving significant industrial wastewater fractions.

Read Full Abstract10.13205/j.hjgc.202604012