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Showing 24 of 1398 peer-reviewed translated articles (Page 36 of 59)

Characteristics and Meteorological Causes of PM2.5-O3 Compound Pollution in Typical Cities of the Yangtze River Delta RegionGraphical AbstractVerified
Environmental Chemistry2026

Characteristics and Meteorological Causes of PM2.5-O3 Compound Pollution in Typical Cities of the Yangtze River Delta Region

In the context of accelerated urbanization, regional air composite pollution in medium and large urban agglomerations is primarily characterized by PM2.5-O3 compound pollution. To elucidate the meteorological causes of PM2.5-O3 compound pollution in the Yangtze River Delta (YRD) region over the recent seven years (2017–2023), this study analyzed monitoring data from typical cities (Nanjing, Shanghai, Hangzhou, and Hefei) using Pearson and partial correlation coefficients. Results indicate: (1) PM2.5 pollution exhibited a significant downward trend across all four cities, with notable improvement during the COVID-19 pandemic in 2020, underscoring the effectiveness of air pollution control measures. Conversely, O3 pollution remained elevated or increased in some cities, indicating persistent challenges in O3 control. (2) During O3 pollution episodes, PM2.5 and O3 concentrations were positively correlated, whereas during PM2.5 pollution episodes, they were negatively correlated. (3) Compound pollution days were predominantly observed from February to October, with the highest frequency (20 days) occurring from April to June. (4) The significant reduction in PM2.5 weakened the aerosol 'umbrella effect', enhancing surface radiation and promoting near-surface O3 formation. Concurrently, changes in the NOx/VOCs ratio weakened O3 titration, and climate warming accelerated O3 precursor generation and potentially altered boundary layer structure, collectively contributing to O3 accumulation in the cold season and an increasing frequency of compound pollution during that period. (5) The formation mechanisms of PM2.5 and O3 are driven by distinct meteorological conditions, with low overall concentration correlation; however, under compound meteorological conditions such as high temperature, stagnant air, and weak diffusion, both pollutants tend to rise synchronously, indicating that compound pollution events are typically driven by multiple adverse meteorological factors. This study demonstrates that from 2017 to 2023, PM2.5 pollution significantly decreased while O3 pollution showed an increasing trend. Compound pollution was concentrated in April–June and influenced by high temperature, stagnant air, and weak diffusion. With effective PM2.5 control, enhanced surface radiation and changes in O3 precursors led to O3 accumulation in the cold season, increasing compound pollution frequency. Overall, compound pollution is driven by multiple meteorological factors, posing complex challenges for control.

Read Full Abstract10.7524/j.issn.0254-6108.2025030602
Bioavailability and Desorption Kinetics of Sulfonamide Antibiotics in Soil Assessed by Diffusive Gradients in Thin-FilmsGraphical AbstractVerified
Environmental Chemistry2026

Bioavailability and Desorption Kinetics of Sulfonamide Antibiotics in Soil Assessed by Diffusive Gradients in Thin-Films

The diffusive gradients in thin-films (DGT) technique has emerged as a promising tool for assessing the desorption kinetics and bioavailability of organic contaminants in soil. This study compared DGT, soil solution, and organic solvent extraction methods for evaluating the bioavailability of four sulfonamide antibiotics (SAs) in soil using pot experiments with Brassica rapa subsp. chinensis and Lactuca sativa. Results demonstrated that plant uptake of SAs depended on compound properties and plant species, with roots as the primary accumulation site. DGT-measured concentrations (CDGT) showed significant linear correlations with SA concentrations in both roots and leaves, and effective concentrations (CE) were positively correlated with plant tissue levels (P < 0.05). The soil solution method also showed predictive ability but with lower stability. The mass of SAs adsorbed by DGT increased non-linearly with deployment time, indicating that solid-phase resupply sustained long-term DGT uptake. DIFS model-derived soil-water partition coefficients (Kdl) ranged from 0.23 to 1.25 mL·g−1, with higher Kdl values corresponding to greater bioavailability. Response times (Tc) ranged from 2307 to 7523 seconds, with sulfamethoxazole (SMZ) exhibiting the highest Tc, indicating its release was most constrained. Meta-analysis of desorption parameters for other organic contaminants revealed that soil pH and particle size were key determinants of Kdl, while molecular volume and hydrophobicity influenced resupply rates. This study confirms the reliability of DGT for assessing antibiotic bioavailability in soil and provides fundamental data on their migration and fate.

Read Full Abstract10.7524/j.issn.0254-6108.2025031001
Optimized Simulation of HONO Sources and Its Impact on Nitrate Formation in GuangzhouGraphical AbstractVerified
Environmental Chemistry2026

Optimized Simulation of HONO Sources and Its Impact on Nitrate Formation in Guangzhou

Nitrous acid (HONO) is a critical precursor of hydroxyl radicals (·OH) in the atmosphere, influencing oxidative capacity and secondary pollutant formation. However, model simulations often underestimate HONO concentrations, and its role in nitrate formation remains unclear. This study investigates a typical winter haze episode in Guangzhou (January 2021, peak PM2.5: 243.0 μg·m−3) using observational data and a box model to quantify HONO sources and assess their impact on ·OH and particulate nitrate. HONO concentrations increased from (1.0±1.0) μg·m−3 during clean periods to (9.2±3.8) μg·m−3 during polluted periods, while nitrate rose from (6.4±3.4) to (43.3±20.0) μg·m−3 (6.8-fold). Incorporating seven additional HONO sources improved simulated daytime HONO from (0.3±0.1) to (6.5±2.3) μg·m−3, matching observations. Source apportionment showed direct vehicle emissions dominated (49.7%), followed by heterogeneous photosensitized reaction of NO2 on aerosol surfaces (23.0%), ground surface reaction (10.7%), and nitrate photolysis (8.7%). With optimized HONO, simulated daytime ·OH increased from (0.6±0.3)×10^6 to (1.5±0.8)×10^6 molec·cm−3 (1.2-fold), and nitrate production via ·OH+NO2 increased from (3.4±1.2) to (15.3±8.5) μg·m−3·h−1 (3.5-fold). The simulated-to-observed nitrate ratio improved from 21% to 81%. Sensitivity tests indicated that setting nitrate photolysis enhancement to 100 times gaseous nitric acid yielded better HONO and nitrate simulations. This study underscores the importance of refining HONO sources for accurate simulation of atmospheric oxidation and nitrate formation, aiding pollution control strategies.

Read Full Abstract10.7524/j.issn.0254-6108.2025081103
Evolution of Water-Soluble Ions in PM2.5 in the Northern Suburbs of Nanjing During Summer Before and After the Implementation of the Air Pollution Prevention and Control Action PlanGraphical AbstractVerified
Environmental Chemistry2026

Evolution of Water-Soluble Ions in PM2.5 in the Northern Suburbs of Nanjing During Summer Before and After the Implementation of the Air Pollution Prevention and Control Action Plan

To assess the impact of the Air Pollution Prevention and Control Action Plan (APPCAP) on the chemical composition of PM2.5, this study analyzed the concentrations, existing forms, and sources of water-soluble ions in PM2.5 collected during summer (June–August) in the northern suburbs of Nanjing for the years 2012, 2013, 2017, and 2019. The results demonstrate a significant reduction in total water-soluble ion concentrations in 2017–2019 compared to 2012, indicating the effectiveness of APPCAP in mitigating PM2.5 pollution. Sulfate (SO4^2−), nitrate (NO3^−), and ammonium (NH4^+) (collectively SNA) were the dominant ionic species, contributing 69.98%–92.58% of the total ion mass, with SO4^2− being the most abundant. In the summers of 2013 and 2017, PM2.5 exhibited alkaline properties, and SNA primarily existed as NH4NO3 and (NH4)2SO4. Conversely, in 2019, PM2.5 became acidic, with SNA present as NH4NO3 and NH4HSO4. The nitrogen oxidation ratio (NOR) and sulfur oxidation ratio (SOR) indicated that NO3^− and SO4^2− predominantly originated from secondary reactions, with SO2 undergoing secondary conversion more readily than NO2, and the degree of secondary conversion increasing annually. Source apportionment revealed a shift from long-range transport in 2013 to local and regional sources by 2017. These findings underscore the success of APPCAP in reducing primary emissions and altering the chemical speciation of secondary inorganic aerosols, while highlighting the persistent dominance of sulfate and the need for continued SO2 emission controls.

Read Full Abstract10.7524/j.issn.0254-6108.2025021901
Comprehensive Evaluation of Soil Quality under Different Vegetation Types in the Green Heart Area of the Changsha-Zhuzhou-Xiangtan City ClusterGraphical AbstractVerified
Environmental Chemistry2026

Comprehensive Evaluation of Soil Quality under Different Vegetation Types in the Green Heart Area of the Changsha-Zhuzhou-Xiangtan City Cluster

The effects of different vegetation types on soil quality in the Green Heart Area of the Changsha-Zhuzhou-Xiangtan City Cluster were evaluated to provide a reference for selecting suitable afforestation species and improving forest soil quality. Seven vegetation types (mixed forest, broad-leaved forest, coniferous forest, economic forest, shrub forest, grassland, and abandoned cropland) with similar site conditions were studied. Eleven soil physicochemical indicators were measured, and soil quality was assessed using principal component analysis (PCA), Pearson correlation, total data set (TDS), minimum data set (MDS), and entropy-weighted TOPSIS methods. Results showed no significant differences in soil water content, soil bulk density, and C:N ratio among vegetation types, while significant differences were found in total porosity, capillary porosity, saturated water content, field water holding capacity, total carbon, total nitrogen, available potassium, and available phosphorus. Compared with abandoned cropland, soil water content, total porosity, field water holding capacity, saturated water content, total carbon, total nitrogen, available potassium, and available phosphorus were significantly higher, and soil bulk density was significantly lower. Mixed forest soil exhibited the highest values for field water holding capacity, total porosity, saturated water content, total nitrogen, total carbon, available potassium, and available phosphorus. Correlation analysis revealed that soil bulk density was extremely significantly negatively correlated with soil water content, total porosity, and saturated water content, and significantly negatively correlated with field water holding capacity, total carbon, and total nitrogen. Soil capillary porosity, field water holding capacity, total porosity, and saturated water content were extremely significantly positively correlated with soil nutrients, while soil bulk density showed varying degrees of negative correlation with soil chemical nutrients. Soil chemical properties and stoichiometric ratios showed varying degrees of significant positive correlation. The order of soil quality under different vegetation types was mixed forest > broad-leaved forest > shrub forest > economic forest > grassland > coniferous forest > abandoned cropland. Mixed forest soil quality was the best and significantly higher than other vegetation types, with significant differences among vegetation types. Mixed forest soil quality was clearly superior. In vegetation restoration and plantation establishment in the Green Heart Area, the principle of matching tree species to site conditions should be followed, with a focus on mixed forests to improve overall soil quality and enhance ecological benefits of artificial vegetation restoration.

Read Full Abstract10.7524/j.issn.0254-6108.2024122406
Phosphorus-Enriched Biochar Promotes Brassica napus L. Growth under Cadmium Stress by Immobilizing Cadmium and Sustained Phosphorus ReleaseGraphical AbstractVerified
Environmental Chemistry2026

Phosphorus-Enriched Biochar Promotes Brassica napus L. Growth under Cadmium Stress by Immobilizing Cadmium and Sustained Phosphorus Release

Cadmium (Cd) contamination in farmland soils poses a threat to food security, necessitating effective remediation strategies. This study prepared three types of phosphorus-enriched biochar (PBC) from rice straw and different phosphorus sources (fused calcium magnesium phosphate, citric acid-activated fused calcium magnesium phosphate, and monocalcium phosphate) to evaluate their potential in stabilizing Cd(II), releasing phosphorus, and enhancing plant resistance to heavy metal stress. Under Cd stress, PBC amendments significantly improved soil physicochemical properties and reduced Cd bioavailability through direct immobilization (adsorption, precipitation) and indirect mechanisms. Specifically, CBC and MBC treatments reduced DTPA-extractable Cd by 45.73% and 48.92%, respectively. The porous structure of biochar facilitated sustained phosphorus release, influencing soil solution phosphorus dynamics. In pot experiments with Brassica napus L., PBC application significantly improved agronomic traits and reduced oxidative stress markers. The C5 treatment increased leaf area by 100%, M7 increased plant height by 26.8%, and M3 reduced malondialdehyde (MDA) and hydrogen peroxide (H2O2) contents by 72.5% and 61.2%, respectively. These findings demonstrate that PBC effectively alleviates Cd toxicity, promotes plant growth, and enhances stress resistance, offering a feasible strategy for remediating Cd-contaminated soils while providing a sustainable phosphorus source.

Read Full Abstract10.7524/j.issn.0254-6108.2025011002
Advances in Computational Simulation of Autoxidation Reactions of Atmospheric Peroxyalkyl RadicalsGraphical AbstractVerified
Environmental Chemistry2026

Advances in Computational Simulation of Autoxidation Reactions of Atmospheric Peroxyalkyl Radicals

Volatile organic compounds (VOCs) are key precursors of secondary organic aerosols (SOA), and their oxidation reactions are regulated by reactive intermediates. A deep understanding of the reaction mechanisms of VOCs-derived reactive intermediates is crucial for evaluating SOA formation. Atmospheric peroxyalkyl radicals (RO2·) are important intermediates produced during VOCs oxidation and can generate highly oxygenated organic molecules (HOMs) through a unique atmospheric autoxidation mechanism, contributing significantly to SOA formation. This article reviews recent advances in computational studies on the autoxidation mechanisms of RO2· with different functional groups, focusing on the autoxidation reactions of RO2· derived from alkanes, alkenes, carbonyl compounds, aromatic hydrocarbons, heteroatom-containing compounds, and other substances. The review highlights the commonalities and differences in autoxidation mechanisms across these functional groups, emphasizing the role of intramolecular hydrogen shifts and subsequent O2 addition steps. Furthermore, we emphasize that future research should focus on the autoxidation of second-generation RO2· and autoxidation mechanisms driven by different intramolecular reactions. Quantum chemical calculations, often combined with kinetic modeling, provide molecular-level insights into reaction pathways and rate constants, which are essential for predicting HOM formation and SOA yields. This review aims to guide further theoretical investigations and support the development of more accurate atmospheric chemistry models.

Read Full Abstract10.7524/j.issn.0254-6108.2025021903
Chemical Characteristics and Source Apportionment of Typical High Mountain Precipitation in the Hengduan Mountains AreaGraphical AbstractVerified
Environmental Chemistry2026

Chemical Characteristics and Source Apportionment of Typical High Mountain Precipitation in the Hengduan Mountains Area

This study analyzed 75 precipitation samples collected from August 2017 to August 2018 in the Meili Snow Mountain region of the Hengduan Mountains. The chemical characteristics of inorganic ions and their seasonal variations between monsoon and non-monsoon periods were examined. The volume-weighted mean total ion concentration was 246.2 μeq·L–1, with higher concentrations in the non-monsoon season and lower in the monsoon season. The dominant water chemistry type was HCO3–-Ca2+. Principal component and partial correlation analyses indicated that Ca2+, Mg2+, HCO3–, and SO42– mainly originated from local sedimentary rock dust, while Na+ and Cl– were primarily marine during the monsoon, with reduced marine influence in the non-monsoon period. NO3– was largely attributed to South Asian pollution emissions, with significant contributions from biomass burning to K+, Na+, and Cl– in the pre-monsoon phase. PMF source apportionment confirmed that during the monsoon, approximately 70% of Cl– and Na+ were from sea salt, whereas in the non-monsoon, over half came from biomass burning. NO3– was almost entirely from fossil fuel combustion during the monsoon (96%), decreasing to 72% in the non-monsoon. Ca2+ and Mg2+ were mainly from carbonate dust in the monsoon and weathered dust in the non-monsoon. Backward trajectory analysis showed that the non-monsoon period was dominated by westerly transport (60%), while the monsoon was dominated by southwest monsoon transport (81%). These findings provide scientific basis for understanding atmospheric pollution and background values in the region.

Read Full Abstract10.7524/j.issn.0254-6108.2025021805
Combined Effects of Biochar and Dissolved Organic Matter Surrogate AQDS on Methane Emissions from Paddy SoilGraphical AbstractVerified
Environmental Chemistry2026

Combined Effects of Biochar and Dissolved Organic Matter Surrogate AQDS on Methane Emissions from Paddy Soil

Paddy soils are a major source of agricultural methane (CH4) emissions. Biochar is widely applied to paddy soils, while dissolved organic matter (DOM) is ubiquitous; both can regulate CH4 emissions by mediating electron transfer processes, yet their synergistic mechanisms remain unclear. This study investigated the individual and combined effects of biochar and the DOM model compound anthraquinone-2,6-disulfonic acid (AQDS) on CH4 emissions from paddy soil during incubation. Biochar amendment increased DOM concentration and accelerated extracellular electron transfer, resulting in a maximum cumulative CH4 emission of (66.23±16.20) μmol, four-fold higher than the control (15.14±0.18) μmol. In contrast, AQDS addition markedly suppressed CH4 accumulation to (1.04±0.09) μmol, attributed to sulfate introduction as a competitive electron acceptor, despite enhanced electron exchange. The combined biochar-AQDS treatment yielded intermediate CH4 accumulation of (12.71±0.32) μmol. Although DOM availability increased, sulfate-driven electron competition inhibited methanogens, and the combined treatment favored the acetoclastic methanogenesis pathway, which produces less CH4 per unit acetate, resulting in lower emissions than biochar alone but higher than AQDS alone, indicating an additive effect. These findings elucidate the mechanisms by which biochar and DOM jointly regulate CH4 emissions from paddy soils, providing a theoretical basis for agricultural management.

Read Full Abstract10.7524/j.issn.0254-6108.2025022801
Characteristics and Source Apportionment of Volatile Organic Compounds at a Roadside Site in a Tropical City during SummerGraphical AbstractVerified
Environmental Chemistry2026

Characteristics and Source Apportionment of Volatile Organic Compounds at a Roadside Site in a Tropical City during Summer

This study conducted online monitoring of volatile organic compounds (VOCs) at a roadside site on a main arterial road in Haikou, a tropical city, during summer 2023 (June 25–September 30). A total of 56 VOCs were measured. The mean total VOC concentration (φ(TVOCs)) was (9.05 ± 6.24) nmol·mol−1, with concentrations in the order: alkanes > alkenes > aromatic hydrocarbons > alkynes, dominated by light alkanes. Alkenes and aromatic hydrocarbons contributed significantly to atmospheric chemical reactivity, while secondary organic aerosol formation potential (SOAFP) was limited, influenced by both VOC concentrations and temperature. VOC concentrations exhibited a pronounced bimodal diurnal pattern, consistent with traffic peaks. Ratio analysis indicated a Toluene/Benzene (T/B) ratio slightly higher than typical vehicle exhaust values, and an iso-Pentane/n-Pentane (i/n) ratio suggesting fuel evaporation influence. Positive Matrix Factorization (PMF) identified four sources: gasoline/LPG vehicle exhaust (49.9%), solvent use or vehicle evaporation (26.1%), diesel vehicle exhaust (14.9%), and biogenic sources (9.1%). SOAFP was mainly contributed by solvent use/evaporation (35.7%), gasoline/LPG exhaust (34.6%), diesel exhaust (22.0%), and biogenic sources (7.7%). These findings indicate that under tropical summer high-temperature conditions, roadside VOC pollution is predominantly traffic-related, with vehicle evaporation sources non-negligible, providing insights for evaluating vehicular impacts on particulate pollution.

Read Full Abstract10.7524/j.issn.0254-6108.2026012804
Electronic Synergy Modulation of Fe-Based Bimetallic Oxides Catalysts for Enhanced Ozonation in Industrial Wastewater TreatmentGraphical AbstractVerified
Environmental Chemistry2026

Electronic Synergy Modulation of Fe-Based Bimetallic Oxides Catalysts for Enhanced Ozonation in Industrial Wastewater Treatment

The design of stable and efficient O3 catalysts is critical for advancing heterogeneous catalytic ozonation (HCO) in industrial wastewater treatment. In this study, various iron-based bimetallic oxides were synthesized, and Fe-Co bimetallic oxide (FeCo-O) was identified as the optimal catalyst through degradation experiments and structural characterization. FeCo-O exhibits a single spinel structure with abundant metal valence states and synergistic effects between Fe and Co. Compared to conventional O3 oxidation, the FeCo-O/O3 system enhanced organic pollutant degradation by 2–3 times, demonstrating broad applicability under neutral or weakly acidic/alkaline conditions. Characterization revealed that FeCo-O promotes O3 activation via enhanced inter-metal electron transfer on the catalyst surface, increasing the generation of highly oxidative free radicals (·OH, ·O2−) and thereby improving pollutant degradation efficiency. In treating real industrial wastewater, the FeCo-O/O3 system achieved excellent COD removal, indicating its potential for both pre-treatment and advanced treatment applications. This study provides theoretical and practical guidance for designing efficient catalytic ozonation catalysts.

Read Full Abstract10.7524/j.issn.0254-6108.2025022502
Formation Mechanisms of Secondary Inorganic Components in Fine Particulate Matter in a Typical City of the Fenwei PlainGraphical AbstractVerified
Environmental Chemistry2026

Formation Mechanisms of Secondary Inorganic Components in Fine Particulate Matter in a Typical City of the Fenwei Plain

Secondary inorganic aerosols (SNA), comprising sulfate, nitrate, and ammonium, are critical contributors to PM2.5 pollution in the Fenwei Plain, yet their formation mechanisms remain poorly characterized. Wintertime observations in Taiyuan revealed SNA as the dominant PM2.5 component, with a mean mass concentration of 33.19 ± 18.72 μg m−3, accounting for 47.13% of total PM2.5 mass. SNA concentrations increased markedly with pollution severity, but even under relatively clean conditions, SNA maintained a high mass fraction. Diurnal variation and correlation analyses indicated that nitrate formation pathways differed between day and night, largely governed by relative humidity (RH). During daytime, high RH (>55%) facilitated the partitioning of gaseous HNO3 to particulate nitrate. At night, RH positively correlated with nitrate concentration and nitrogen oxidation rate (NOR), with increased aerosol liquid water content (AWC) promoting NO2-to-nitrate conversion. The PM2.5 pH ranged from 4.3 to 5.2, and sulfate formation was primarily driven by H2O2 oxidation, with NO2 oxidation as a secondary pathway. These findings enhance understanding of SNA formation in the Fenwei Plain and provide a scientific basis for air quality policy.

Read Full Abstract10.7524/j.issn.0254-6108.2025022704
Distribution and Risk Assessment of Per- and Polyfluoroalkyl Substances from Source Water to Tap Water in the Hubei Section of the Yangtze River MainstreamGraphical AbstractVerified
Environmental Chemistry2026

Distribution and Risk Assessment of Per- and Polyfluoroalkyl Substances from Source Water to Tap Water in the Hubei Section of the Yangtze River Mainstream

Per- and polyfluoroalkyl substances (PFAS) are emerging contaminants of concern in China, and drinking water is a major exposure pathway. This study investigated 17 PFAS in surface water from 12 drinking water sources along the Hubei section of the Yangtze River mainstream during dry, normal, and wet seasons. Total PFAS concentrations ranged from 10.84 to 41.05 ng/L (dry), nd to 62.60 ng/L (normal), and 6.77 to 29.00 ng/L (wet). Predominant compounds were PFBS, PFOA, PFHxA, PFBA, and PFOS. Lake-type sources exhibited significantly higher concentrations than river-type sources, and dry and normal seasons showed higher levels than wet season. Compared to other Chinese sources, PFAS levels in Hubei were moderate, with fluorochemical plant inputs and population density as likely influencing factors. Ecological and health risk assessments indicated acceptable risks. In four selected water supply systems, PFAS distribution from source to tap was examined; PFOA, PFBA, PFHxA, and PFBS were dominant, and secondary water supply did not significantly introduce or remove PFAS. Health risks from tap water were within acceptable limits.

Read Full Abstract10.7524/j.issn.0254-6108.2025100102
Adsorption Behavior of Microplastics for Typical Psychoactive DrugsGraphical AbstractVerified
Journal of Environmental Engineering Technology2026

Adsorption Behavior of Microplastics for Typical Psychoactive Drugs

Microplastics, as emerging environmental pollutants, can adsorb psychotropic drugs in aquatic environments, facilitating their migration and transformation, ultimately posing ecological risks. This study investigated the adsorption behavior and mechanisms of four common microplastics—polyethylene (PE), polypropylene (PP), polystyrene (PS), and polyvinyl chloride (PVC)—each with a particle size of 50 μm, toward three psychoactive drugs: diazepam, fluoxetine, and mianserin. Adsorption kinetics, isotherms, and the effects of pH and salinity were examined. Kinetic data fitted well to a pseudo-second-order model, indicating chemisorption as the rate-limiting step. Isotherm analysis using Langmuir and Freundlich models revealed that PE exhibited the highest affinity for fluoxetine, PP for mianserin, and PVC for diazepam, while PS showed linear adsorption for fluoxetine, suggesting partitioning. The adsorption of diazepam was maximal at pH 6.5–8.5, typical of natural surface waters, and increased with NaCl concentration, indicating that non-electrostatic interactions dominate and that higher ionic strength enhances adsorption. Mechanistic insights suggest that hydrophobic interactions, hydrogen bonding, π-π interactions (for PS), and halogen bonding (for fluoxetine) contribute to adsorption. These findings highlight the potential of microplastics to act as vectors for psychoactive drugs, necessitating further research on their environmental fate and ecological implications.

Read Full Abstract10.13205/j.hjgc.202606014
Research Advances in Resin-Enhanced Electrosorption for Water TreatmentGraphical AbstractVerified
Journal of Environmental Engineering Technology2026

Research Advances in Resin-Enhanced Electrosorption for Water Treatment

Resin-enhanced electrosorption for water treatment significantly improves ion adsorption efficiency and selectivity through synergistic effects, making it a research hotspot in the water treatment field. This technology provides an innovative solution to the bottlenecks of kinetic lag and insufficient selectivity by modulating electrode-solution interface behavior in multiple dimensions. Current technological advances include the following: a simple integration method enables desalination efficiency to exceed 92.3%; resin-coated composite electrodes eliminate the co-ion effect and achieve a 42% increase in total salt adsorption capacity; resin-derived porous carbon electrodes with tunable pore structures possess three to five times the adsorption capacity of commercially available activated carbon; and by enhancing solution convection and electrophoretic convection, the resin-filling strategy achieves a high desalination rate of (670 ± 20) mg/(L·h). Studies have demonstrated that different material combinations can achieve targeted optimization of adsorption performance based on specific water quality characteristics. Future research directions may focus on: developing intelligent resin materials with electromagnetic responsiveness; constructing a multi-scale structural design theory for resin-electrode systems; and establishing a cross-scale model integrating electrochemistry, fluid dynamics, and interface science for comprehensive analysis. In particular, in-depth studies are needed on the dynamic behavior of resin-based flow electrodes under electric/magnetic field regulation, as well as the precise construction of catalytic sites on the resin surface. This review aims to promote the widespread application and efficient practice of this technology in water treatment, providing a theoretical foundation and scientific basis for the future development of high-efficiency, selective, and stable electrosorption technologies.

Read Full Abstract10.13205/j.hjgc.202606008
Performance and Mechanism of Cobalt-Aluminum Spinel Catalyzed Oxidation of Nitric OxideGraphical AbstractVerified
Journal of Environmental Engineering Technology2026

Performance and Mechanism of Cobalt-Aluminum Spinel Catalyzed Oxidation of Nitric Oxide

Cobalt-aluminum spinel metal oxides derived from hydrotalcite were synthesized via hydrothermal, coprecipitation, and sol-gel methods, and their catalytic performance for NO oxidation was systematically evaluated. Characterization by X-ray photoelectron spectroscopy (XPS), O2 temperature-programmed desorption (O2-TPD), H2 temperature-programmed reduction (H2-TPR), and Raman spectroscopy revealed that the synthesis method significantly influences the surface Co2+/Co3+ ratio, which in turn modulates the formation of surface oxygen vacancies. The hydrothermally synthesized catalyst (CoAlO-H) exhibited the highest density of surface oxygen vacancies, leading to enhanced adsorption and activation of gaseous oxygen and superior NO oxidation activity compared to coprecipitation (CoAlO-C) and sol-gel (CoAlO-S) counterparts. Mechanistic studies using NO-TPD, NO+O2-TPD, and in situ diffuse reflectance infrared Fourier transform spectroscopy (in situ DRIFTS) identified nitrates as key intermediates. Notably, CoAlO-C and CoAlO-S followed the Langmuir-Hinshelwood (L-H) mechanism, whereas CoAlO-H operated via both L-H and Mars-van Krevelen (MvK) mechanisms. The exceptional performance of CoAlO-H is attributed to its abundant surface oxygen vacancies, high surface oxygen mobility, and low decomposition temperature of reaction intermediates. These findings provide a rational basis for designing efficient non-precious metal catalysts for NO oxidation in diesel exhaust aftertreatment.

Read Full Abstract10.13205/j.hjgc.202606007
Comparative Analysis of CH4 and N2O Generation and Emission Characteristics in A2/O and A2/O-MBR Wastewater Treatment PlantsGraphical AbstractVerified
Journal of Environmental Engineering Technology2026

Comparative Analysis of CH4 and N2O Generation and Emission Characteristics in A2/O and A2/O-MBR Wastewater Treatment Plants

The A2/O-MBR process, owing to its superior effluent quality and smaller footprint, is increasingly adopted in newly built and upgraded wastewater treatment plants. However, systematic studies on its greenhouse gas (GHG) emissions remain scarce, and direct comparisons with the conventional A2/O process are lacking. In this study, two full-scale wastewater treatment plants employing the A2/O and A2/O-MBR processes under identical influent conditions, climate, and discharge standards were investigated. A high-frequency monitoring system covering the entire treatment train was established, and combined with measurements of dissolved CH4 and N2O, water quality parameters, and operational parameters, to elucidate the differences in GHG emission characteristics. Results showed that the daily average CH4 emission intensities were not significantly different between the two plants [(0.67 ± 0.22) and (0.65 ± 0.18) g/m3, respectively]. CH4 emissions mainly originated from sewer-derived anaerobic production and subsequent release in the pretreatment units (accounting for over 70% of the total emissions), with partial in-plant oxidation by methanotrophs. Temperature and aeration-induced stripping were identified as key driving factors, as CH4 emissions were positively correlated with ambient temperature and dissolved oxygen (DO). In contrast, more than 90% of N2O emissions occurred in the biological treatment units. The A2/O-MBR plant exhibited significantly higher daily N2O emission intensity [(0.132 ± 0.055) g/m3] than the A2/O plant [(0.060 ± 0.046) g/m3], largely due to intensive aeration and oxygen-enriched internal/external recirculation in the membrane tank, which enhanced N2O production and stripping. Correlation analysis further revealed that N2O emissions in the A2/O plant were positively related to influent COD and BOD5, indicating dominance of heterotrophic denitrification, whereas in the A2/O-MBR process they were mainly driven by NH3-N loading and DO, reflecting a nitrification-based pathway. Importantly, both processes exhibited CH4 and N2O emission factors that were significantly lower than the reference values recommended by the IPCC and industry guidelines, underscoring the necessity of localizing emission factors for accurate carbon accounting.

Read Full Abstract10.13205/j.hjgc.202606013
Oxygen-Loaded Porous Materials Inhibit Phosphorus Release at the Sediment-Water Interface in Eutrophic WatersGraphical AbstractVerified
Journal of Environmental Engineering Technology2026

Oxygen-Loaded Porous Materials Inhibit Phosphorus Release at the Sediment-Water Interface in Eutrophic Waters

Dissolved oxygen (DO) is a critical factor controlling endogenous phosphorus (P) migration in eutrophic waters. Existing oxygenation technologies suffer from high energy consumption and sediment disturbance, necessitating low-disturbance, pH-stable strategies that avoid additional nitrogen and P loads. This study evaluated an oxygen-loaded porous material (OLPM) for inhibiting sediment P release using laboratory microcosms with natural eutrophic water samples. DO microprofiles across the sediment-water interface (SWI) were measured with microelectrodes; diffusive gradients in thin films (DGT) resolved Fe, S, and P distributions; and sequential extraction quantified sediment P fractions. Results showed that OLPM coverage increased surface sediment DO concentration by 6.58-fold and DO penetration depth by 1.33-fold (16.8 mm). Overlying water total phosphorus (TP) decreased by 93.79%, and sediment interstitial phosphate (PO4-P) decreased by up to 45.75%. The SWI TP exchange flux reversed from +0.0068 mg/(m2·d) to -0.014 mg/(m2·d), shifting the system from a P source to a P sink. Sediment P fractionation revealed a 5.22% increase in stable Res-P and a 4.48% decrease in labile NaHCO3-P. Mechanistically, OLPM enhanced iron oxidation (Fe2+ reduced by 59.62%) and suppressed sulfate reduction (S2- homogenized at low levels), promoting P immobilization via Fe-S coupling. The material effectively inhibits endogenous P release through interfacial DO regulation without altering pH, offering a promising approach for eutrophication management.

Read Full Abstract10.13205/j.hjgc.202606010
Preparation of Dispersed Iron-Sulfur-Based Nanoparticle Slurry and Its Application in Remediating Cr(VI) ContaminationGraphical AbstractVerified
Journal of Environmental Engineering Technology2026

Preparation of Dispersed Iron-Sulfur-Based Nanoparticle Slurry and Its Application in Remediating Cr(VI) Contamination

Hexavalent chromium (Cr(VI)) contamination in chromite ore processing residue (COPR) and associated soils poses a persistent environmental challenge. This study developed a dispersedly stabilized iron-sulfur-based slurry (DSS-ISB) modified with an inorganic dispersant to enhance nanoparticle suspension stability and interfacial reactivity. The slurry, with a particle size of approximately 200 nm, efficiently reduced and immobilized Cr(VI) without pH adjustment. Under optimal conditions (liquid-to-solid ratio of 5 mL:10 g, DSS-ISB dosage of 1.8 mg/g, reaction time of 20 h), the removal efficiency exceeded 97%, reducing the leaching concentration from 15.03 mg/L to 0.03 mg/L, well below the GB 5085.3—2007 limit of 5 mg/L. X-ray photoelectron spectroscopy (XPS) and Brunauer-Emmett-Teller (BET) analyses revealed a synergistic mechanism of chemical reduction (Fe2+/S2- as dual electron donors) and surface adsorption, converting toxic Cr(VI) to stable Cr(III). Compared with traditional reductants ferrous sulfate (FeSO4) and sodium sulfide (Na2S), DSS-ISB increased removal efficiency by 28.24% and 6.23%, respectively, and unit mass removal capacity by 92.43% and 77.08%. The reagent cost per ton of COPR was reduced to RMB 36.40, achieving savings of 33.82% and 26.02% versus FeSO4 (RMB 55.00) and Na2S (RMB 49.20). The process eliminates pH adjustment and subsequent passivation, simplifying remediation. DSS-ISB offers an economical and green solution for Cr(VI) remediation in both industrial residues and contaminated soils.

Read Full Abstract10.13205/j.hjgc.202606011
Machine Learning-Based Prediction of Acidogenic Performance in Anaerobic Fermentation of Chemical-Biological Sewage SludgeGraphical AbstractVerified
Journal of Environmental Engineering Technology2026

Machine Learning-Based Prediction of Acidogenic Performance in Anaerobic Fermentation of Chemical-Biological Sewage Sludge

Municipal sludge anaerobic resource recovery efficiency in China lags behind developed countries. Widespread chemical phosphorus removal increases iron and aluminum salt precipitates in waste activated sludge, forming chemical-biological sludge that reduces acidogenic efficiency. This study identified key factors and developed a high-precision prediction model. Integrating literature and experimental data, acidogenic performance indicators under various conditions were compiled. Five machine learning models—Backpropagation Neural Network, Adaptive Neuro-Fuzzy Inference System, Support Vector Machine, K-Nearest Neighbors, and Random Forest—were systematically compared. Random Forest achieved the best predictive performance with a test set coefficient of determination (R²) of 0.9463, significantly outperforming others with minimal overfitting risk, demonstrating strong capability for high-dimensional, nonlinear, multi-factor coupled problems. Feature importance analysis revealed pH and Volatile Suspended Solids (VSS) as primary drivers, with aluminum salts exerting greater influence than iron salts. Engineering optimization should follow the pathway: 'adjust pH, stabilize organic matter, control aluminum salts'. This study provides an intelligent predictive tool and clarifies optimization directions, advancing precision and intelligent sludge treatment.

Read Full Abstract10.13205/j.hjgc.202606001
Recent Progress in Chitosan-Based Microsphere Composites for Phosphorus Removal from Aqueous EnvironmentsGraphical AbstractVerified
Journal of Environmental Engineering Technology2026

Recent Progress in Chitosan-Based Microsphere Composites for Phosphorus Removal from Aqueous Environments

Chitosan-based microsphere composites have attracted considerable attention for phosphorus adsorption due to their facile preparation, low cost, environmental friendliness, and high uptake capacity. This review summarizes the physicochemical properties and preparation methods of chitosan microspheres for phosphate removal, outlines common modification strategies to enhance adsorption capacity, and discusses their applications in aqueous environments. Adsorption mechanisms, regeneration, and resource recovery of spent microspheres are analyzed. Challenges and recommendations are proposed, including streamlined preparation, enhanced phosphorus recovery, removal of multiple phosphorus forms, and practical implementation. The review aims to guide the development of high-performance chitosan-based microspheres for phosphorus removal.

Read Full Abstract10.13205/j.hjgc.202606006
Environmental Impact and Cost Analysis of Ecological Buffer Zones from an LCA-LCC PerspectiveGraphical AbstractVerified
Journal of Environmental Engineering Technology2026

Environmental Impact and Cost Analysis of Ecological Buffer Zones from an LCA-LCC Perspective

To identify optimal watershed remediation pathways under environmental and economic dimensions, an integrated environmental-economic impact assessment framework combining life cycle assessment (LCA) and life cycle costing (LCC) based on openLCA was established, using 1 m³ of treated wastewater as the functional unit. This framework comprehensively evaluated the environmental impacts and economic costs of three ecological buffer measures—constructed wetlands, ecological intercepting ditches, and vegetation restoration projects—in non-point source pollution control. The results indicated that constructed wetlands offer the optimal environmental-economic profile, featuring the lowest comprehensive cost (¥1.01 yuan/m³) and the lowest load across most environmental impact categories, with only slightly higher land resource consumption intensity. Ecological intercepting ditches exhibited higher impacts in areas such as metal resource consumption due to the use of rebars and base fertilizer inputs, resulting in a moderate comprehensive cost (¥1.57 yuan/m³). Vegetation restoration projects incurred the highest comprehensive cost (¥61.14 yuan/m³) and produced the most significant environmental impacts, with elevated indicators such as human carcinogenic toxicity. This primarily stemmed from the extensive use of concrete grass pavers and base fertilizer in rural river sections. These findings provide quantitative references for environmental-economic integrated evaluation and decision-making regarding ecological buffer zone engineering schemes in similar watersheds.

Read Full Abstract10.13205/j.hjgc.202606004
High-Temperature Dechlorination Performance of Solid Waste-Based Dechlorination AgentsGraphical AbstractVerified
Journal of Environmental Engineering Technology2026

High-Temperature Dechlorination Performance of Solid Waste-Based Dechlorination Agents

The escalating volume of municipal solid waste in China necessitates effective disposal strategies. Industrial kiln co-processing offers a promising route, but high-temperature decomposition of chlorinated components releases HCl and Cl2, causing severe equipment corrosion and operational issues. This study investigates the high-temperature dechlorination performance of fly ash and red mud, two abundant industrial solid wastes, as potential dechlorination agents. Using a high-temperature tube furnace system, dechlorination efficiencies were evaluated across 600–900 °C. At 700 °C, fly ash achieved a peak dechlorination efficiency of 93.33%, while red mud reached 88.61%. However, efficiencies declined with further temperature increase, dropping to 65.6% and 58.27% at 900 °C for fly ash and red mud, respectively. To enhance performance at higher temperatures, fly ash was modified via alkali (NaOH) treatment. The modification increased surface roughness and porosity, disrupted Si-O-Si and Si-O-Al networks, and exposed active sites. Consequently, the alkali-modified fly ash exhibited a peak dechlorination efficiency of 94.98% at 800 °C, a 23.08% improvement over unmodified fly ash (71.9%). These findings demonstrate the technical feasibility of utilizing solid wastes as dechlorination agents, offering a dual benefit of waste valorization and cost-effective high-temperature gas purification. The study provides a foundation for scaling up this approach in industrial kiln applications, contributing to sustainable waste management and reduced environmental impact.

Read Full Abstract10.13205/j.hjgc.202606009
Establishment of a Carbon Emission Balance Model and Analysis of Carbon Neutrality Pathways for Urban Reclaimed Water PlantsGraphical AbstractVerified
Journal of Environmental Engineering Technology2026

Establishment of a Carbon Emission Balance Model and Analysis of Carbon Neutrality Pathways for Urban Reclaimed Water Plants

In the context of carbon peaking and carbon neutrality, urban reclaimed water plants must adopt measures such as energy conservation, consumption reduction, and enhanced resource and energy utilization to achieve carbon neutrality. This study developed a carbon emission balance model and accounting method for such plants, incorporating strategies of carbon emission reduction, carbon substitution, and carbon sink. The optimal pathway towards carbon neutrality was evaluated based on the carbon emission balance ratio. Using a 1×10⁵ m³/d urban reclaimed water plant as a case study, the results showed total carbon emissions of 20,934 t CO2e. The carbon emission reduction from reclaimed water source heat pumps for heating and cooling was 21,701 t CO2e, yielding a carbon emission balance ratio of 103.7%. In contrast, other carbon reduction measures contributed 15,424 t CO2e, with a balance ratio of 73.7%, highlighting the pivotal role of reclaimed water source heat pumps. When the heat pump extracted 27% and 36% of residual thermal energy, coupled with reclaimed water reuse or sludge anaerobic digestion-cogeneration, respectively, both pathways achieved a 100% balance ratio. Assuming year-round extraction, the balance ratio reached 213%. The carbon reduction ratio between utilizing residual thermal energy and chemical energy was 8.76:1. This study demonstrates that urban reclaimed water plants can achieve carbon neutrality through multiple pathways, with residual thermal energy recovery exhibiting significant potential.

Read Full Abstract10.13205/j.hjgc.202606005