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All Clean Energy & Battery Intelligence (Page 19)

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Showing 24 of 1398 peer-reviewed translated articles (Page 19 of 59)

Fabrication and Microwave Absorption Performance of FexOy/TiO2/C Composites Derived from Red MudGraphical AbstractVerified
Journal of Fuel Chemistry and Technology2026

Fabrication and Microwave Absorption Performance of FexOy/TiO2/C Composites Derived from Red Mud

Red mud, an industrial solid waste from alumina production, poses severe environmental challenges. This study presents a resource-efficient strategy to convert red mud into high-performance microwave absorbing materials. FexOy/TiO2/C composites were synthesized via a sol-gel method using starch as carbon source, followed by carbothermal reduction. The phase composition and microstructure were optimized by adjusting calcination temperature and raw material ratio. The optimal sample, RmCT-5.4-700, exhibited a minimum reflection loss (RLmin) of -30.2 dB at 14.0 GHz with an effective absorption bandwidth (EAB) of 5.3 GHz at a coating thickness of 2.0 mm. The superior absorption performance is attributed to the synergistic effects of dielectric components (TiO2, graphitized carbon) and magnetic components (Fe3O4/Fe). Carbothermal reduction introduces defects that induce dipole polarization, while the conductive network formed by graphitized carbon and Fe3O4/Fe particles enhances conductive loss. Heterogeneous interfaces between Fe3O4, Fe, TiO2, and the red mud matrix promote interfacial polarization. The magnetic loss of Fe3O4/Fe improves impedance matching, facilitating electromagnetic wave penetration and absorption. This work not only provides a novel route for red mud valorization but also contributes to the high-value utilization of solid wastes.

Read Full Abstract10.3724/2097-213X.2025.JFCT.0021
Damage Mechanism of High Chromia Refractory in the Slag Tapping Hole of Commercial Entrained-Flow GasifiersGraphical AbstractVerified
Journal of Fuel Chemistry and Technology2026

Damage Mechanism of High Chromia Refractory in the Slag Tapping Hole of Commercial Entrained-Flow Gasifiers

The service life of refractory bricks in the slag tapping hole of entrained-flow gasifiers is a critical bottleneck for long-term stable operation. This study investigated the damage mechanism of high chromia refractories in four commercial coal-water slurry gasifiers by analyzing gasification coal samples and corroded refractory bricks. Slag characteristics, including crystallization and viscosity-temperature behavior, were evaluated. Results revealed that low-viscosity slag induces more severe refractory damage. To mitigate slag crystallization risk, a safe slag tapping temperature range is recommended as tICT−t2.5 when tICT exceeds t25. Interior morphology of corroded bricks exhibited cracks, primarily attributed to molten slag penetration and subsequent reactions with refractory material. SEM-EDS analysis of slag-aggregate and slag-matrix interfaces identified reduction in Cr2O3 content as the earliest damage characteristic. XRD detected no zirconium-containing spinel in cracks, indicating that thermal expansion mismatch between newly formed phases and the refractory matrix drives crack propagation. A damage mechanism is proposed: initial Cr2O3 depletion compromises both matrix and aggregate, facilitating slag ingress and new phase formation, ultimately leading to structural failure. Early detection or prevention of Cr2O3 reduction is essential to prolong refractory service life.

Read Full Abstract10.1016/S1872-5813(25)60600-1
Research advances in the pyrolysis recycling of waste wind turbine bladesGraphical AbstractVerified
Journal of Fuel Chemistry and Technology2026

Research advances in the pyrolysis recycling of waste wind turbine blades

The global energy landscape is undergoing a profound transformation, with wind energy gaining increasing prominence due to its clean and renewable nature. However, as installed wind power capacity expands, disposal of waste wind turbine blades (WWTB) has emerged as a significant challenge. These blades are predominantly composed of epoxy resin (EP) polymers, carbon fibers (CFs), and glass fibers (GFs). Improper disposal exacerbates environmental concerns and leads to loss of valuable resources, particularly carbon-based materials. Pyrolysis technology, a versatile and environmentally sustainable method for resource recovery, has garnered considerable attention for WWTB disposal. This work presents a comprehensive review of pyrolytic recycling of WWTB, focusing on principles and classifications of pyrolysis technology, key factors influencing the pyrolysis process, as well as pyrolysis methods, equipment, products, and their applications. Through in-depth analysis of current research, this review identifies critical unresolved issues and provides a forward-looking perspective on emerging research trends. The review highlights that pyrolysis can effectively recover glass fibers and carbon fibers with mechanical property retention depending on process conditions, and that catalytic pyrolysis can enhance the quality of recovered products. Economic analysis indicates that collaborative disposal methods can improve cost-effectiveness. Future research should focus on optimizing process parameters for large-scale industrial application and developing more efficient catalysts to improve product selectivity and fiber quality.

Read Full Abstract10.1016/S1872-5813(25)60617-7
Rapid Identification of Industrial Wastewater Discharges in Municipal Sewer Networks Based on Three-Dimensional Fluorescence Spectroscopy and Spectral Angle MappingGraphical AbstractVerified
Chinese Journal of Environmental Engineering2026

Rapid Identification of Industrial Wastewater Discharges in Municipal Sewer Networks Based on Three-Dimensional Fluorescence Spectroscopy and Spectral Angle Mapping

The increasing complexity of pollutant sources in municipal wastewater networks, driven by unauthorized industrial discharges, poses significant risks to the stable operation of wastewater treatment plants. This study, conducted in an industrial park in Ningbo, Zhejiang Province, developed a source apportionment method using excitation-emission matrix (EEM) fluorescence spectroscopy combined with spectral angle mapping (SAM). A pollution fingerprint database was constructed from wastewater samples of six representative enterprises (A–F) and municipal sewer samples. The SAM algorithm demonstrated high sensitivity and stability in detecting changes in water composition, with spectral angle values showing a strong linear correlation (R² > 0.88) with the volume ratio of enterprise wastewater in mixed samples. This enabled both qualitative identification and quantitative estimation of pollution sources. Field application over a 12-hour monitoring period identified two enterprises as major contributors to organic matter and nitrogen during critical pollution episodes, consistent with trends in DOC, TN, and UV254. The proposed EEM+SAM approach offers a non-invasive, high-throughput method for real-time monitoring and source tracing of multi-source pollution in complex sewer systems, providing a scientific basis for pollution accountability and precise enforcement.

Read Full Abstract10.12030/j.cjee.202507055
Citric Acid-Modified HUSY Zeolite Catalyzes Alkylation of Phenol with Cyclohexanol for High-Density Aviation Fuel PrecursorsGraphical AbstractVerified
Journal of Fuel Chemistry and Technology2026

Citric Acid-Modified HUSY Zeolite Catalyzes Alkylation of Phenol with Cyclohexanol for High-Density Aviation Fuel Precursors

Lignin-derived oxygenated aromatics, particularly phenols and aromatic ethers, are promising feedstocks for synthesizing high-density, high-heat-sink aviation fuels via alkylation-hydrogenation processes. This study systematically evaluates the catalytic performance of various zeolites (Hβ, HZSM-5, MCM-41, and HUSY) in the alkylation of phenol with cyclohexanol. Characterization demonstrates that HUSY zeolite exhibits superior catalytic activity due to its favorable pore architecture and well-balanced acid site distribution, which synergistically facilitate molecular diffusion and catalytic transformations. To further enhance catalytic properties, HUSY was modified with citric acid at various concentrations and compared with NaOH and oxalic acid treatments. Results reveal that citric acid treatment preserves crystallinity while modulating acidity and pore structure. All modified zeolites enhance phenol alkylation activity. Notably, HUSY-0.5M, exhibiting the highest medium-strong acid to total acid ratio, achieves superior performance: 80.4% phenol conversion and 99.6% selectivity for alkylation products. The catalyst also shows high activity for various lignin-derived compounds (p-cresol, anisole, guaiacol), demonstrating broad applicability. This work provides a new strategy for valorizing lignin-derived phenols into high-value fuel precursors through alkylation.

Read Full Abstract10.1016/S1872-5813(25)60581-0
Hydrogen Production and Structure Evolution Mechanism during Thermochemical Conversion of Microalgae Pellet in Molten Hydroxide SaltsGraphical AbstractVerified
Journal of Fuel Chemistry and Technology2026

Hydrogen Production and Structure Evolution Mechanism during Thermochemical Conversion of Microalgae Pellet in Molten Hydroxide Salts

This study investigates the thermochemical conversion behavior of microalgae pellets in a molten hydroxide salt (80% NaOH-20% Na2CO3) system and its influence on hydrogen production. By comparing temperature evolution, gas release characteristics, and structural evolution of pellets with and without molten salt, and integrating char alkalization experiments, the regulatory mechanism of molten salt on reaction pathways and hydrogen production was systematically analyzed. Results indicate that molten salt significantly enhances internal heat transfer efficiency, achieving a central heating rate of 177 °C/s, effectively alleviating thermal hysteresis. Concurrently, molten salt promotes pore development through penetration, erosion, and catalytic effects, resulting in a porosity increase of 53.2%–104.3% after 10 s of reaction. Conversion efficiency is markedly improved, with the dominant reaction pathway shifting to char alkalization after only 70 s. Furthermore, when heating rate is increased above 600 °C, hydrogen yield from char alkalization improves more significantly, primarily attributed to the synergistic promotion of molten salt catalysis and rapid heating on volatiles reforming. This study provides a theoretical foundation for understanding efficient hydrogen production from biomass in molten hydroxide salts.

Read Full Abstract10.3724/2097-213X.2025.JFCT.0024
Recent Advances in CO2 Hydrogenation to Light OlefinsGraphical AbstractVerified
Journal of Fuel Chemistry and Technology2026

Recent Advances in CO2 Hydrogenation to Light Olefins

The catalytic hydrogenation of carbon dioxide (CO2) to light olefins (C2–C4) represents a pivotal route for mitigating greenhouse gas emissions while producing high-value chemical feedstocks. This review systematically examines the two principal technological pathways: CO2-Fischer-Tropsch synthesis (CO2-FTO) and CO2-methanol-to-olefins (CO2-MTO). The CO2-FTO route couples reverse water-gas shift (RWGS) with Fischer-Tropsch synthesis, whereas CO2-MTO proceeds via methanol intermediate. Key challenges arise from the thermodynamic stability of CO2 (C=O bond dissociation energy ~750 kJ/mol) and kinetic limitations. The review critically evaluates the influence of catalyst promoters (e.g., Na, Mn, Cu), support structures, and surface defect site concentrations on CO2 activation and olefin selectivity. For zeolite-based catalysts, pore architecture and acidity are shown to govern methanol conversion to olefins. Representative data from the literature indicate that Fe-based catalysts with Na promotion achieve CO2 conversion up to 40% with olefin selectivity exceeding 50% under optimized conditions. The review underscores the necessity of integrating catalyst design with reactor engineering to overcome thermodynamic constraints and achieve industrially viable performance.

Read Full Abstract10.3724/2097-213X.2025.JFCT.0026
Cu3P@CuO Nanosheet Catalyst for Efficient Hydrolytic Hydrogen Production from Ammonia BoraneGraphical AbstractVerified
Journal of Fuel Chemistry and Technology2026

Cu3P@CuO Nanosheet Catalyst for Efficient Hydrolytic Hydrogen Production from Ammonia Borane

Ammonia borane (AB) is a promising hydrogen storage material due to its low molecular weight and high hydrogen content. The development of low-cost, high-activity catalysts for AB hydrolysis is critical for industrialization. In this work, CuO nanosheets (CuO NS) were synthesized via a solvothermal method under alkaline conditions using anhydrous copper chloride as precursor. Subsequently, low-temperature phosphating converted CuO NS into Cu3P@CuO nanosheets (Cu3P@CuO NS). The morphology and structure were characterized by SEM, TEM, AFM, XRD, and XPS. The catalytic performance for AB hydrolysis was evaluated, revealing that at a phosphating ratio of m(CuO NS)/m(NaH2PO2)=1 (0.1 g each), Cu3P@CuO NS exhibited excellent activity with a TOF of 57.23 min−1 and an apparent activation energy of 44.31 kJ/mol. The reaction followed pseudo-first-order kinetics with respect to catalyst amount and pseudo-zero-order kinetics with respect to AB concentration. The superior performance is attributed to the abundant active sites exposed by the nanosheet structure. Given the extremely low cost, Cu3P@CuO NS is a promising alternative to noble metal catalysts for hydrogen generation from AB.

Read Full Abstract10.3724/2097-213X.2025.JFCT.0020
Methanation Performance of Biomass Gasification Syngas over Alkali-Modified Ni/Al2O3 Monolithic CatalystsGraphical AbstractVerified
Journal of Fuel Chemistry and Technology2026

Methanation Performance of Biomass Gasification Syngas over Alkali-Modified Ni/Al2O3 Monolithic Catalysts

The methanation of biomass gasification syngas (H2/CO = 3:1) was investigated over Ni/Al2O3 monolithic catalysts supported on cordierite, with a nominal Ni loading of 15 wt%. Catalysts were modified by treatment with 10% NaOH solution for 1 h and 2 h. Physicochemical properties were characterized by BET, TEM, H2-TPR, XRD, CO2-TPD, and TG. Results showed that the 2 h modification (15%Ni/Al2O3-2h) increased specific surface area, enhanced catalytic activity, and increased alkaline site density compared to the unmodified catalyst. Under optimized conditions (H2/CO volume ratio 3:1, space velocity 10000 mL/(g·h), temperature 400 °C), the 15%Ni/Al2O3-2h catalyst achieved a CO conversion of 97% and CH4 selectivity of 100%. Stability tests over 2 h showed that the CO conversion remained stable at approximately 98%, indicating excellent catalytic stability. The study demonstrates that alkali modification with 10% NaOH for 2 h significantly improves both the methanation performance and stability of Ni/Al2O3 monolithic catalysts, offering a promising route for synthetic natural gas production from biomass.

Read Full Abstract10.1016/S1872-5813(25)60607-4
Effects of Endogenous Potassium and Calcium Ions on the Yields and Characteristics of Products from Corn Stalk PyrolysisGraphical AbstractVerified
Journal of Fuel Chemistry and Technology2026

Effects of Endogenous Potassium and Calcium Ions on the Yields and Characteristics of Products from Corn Stalk Pyrolysis

Endogenous alkali and alkaline earth metals (AAEMs) in biomass ash and pyrolysis temperature significantly influence the properties of pyrolysis polygeneration products. This study selected potassium (K+) and calcium (Ca2+) as representative AAEMs, added them at mass ratios of 2%, 5%, and 7% to corn stover via impregnation, and conducted fixed-bed pyrolysis at 400, 500, and 600 °C to investigate the yields and compositions of gas, liquid, and solid products. Results showed that increasing metal ion concentration significantly increased biochar yield, with Ca2+ at 7% achieving 24.96% biochar yield, while bio-oil yield generally decreased. Ca2+ strongly promoted H2 formation due to its Lewis acidity, reaching 32.49% in gas at 7% concentration, and facilitated furan enrichment to 65.88%. K+ at low concentrations favored phenolic formation, while high concentrations promoted ketones and intensified bio-oil cracking. Increasing temperature from 400 to 600 °C decreased biochar yield and increased gas yield, with high temperatures enhancing secondary cracking and reforming, significantly raising H2 and CH4 yields while suppressing oxygenates. At 600 °C, K+ catalysis increased acids to 39.41%, while Ca2+ maintained furans at 65.89%. This study demonstrates that adjusting metal ion concentration and temperature enables directional regulation of high-value bio-oil components and high-energy gases, providing a theoretical basis for optimized biomass pyrolysis utilization.

Read Full Abstract10.3724/2097-213X.2025.JFCT.0025
Metal-Free Brush-Like 3D Carbon Nitride Delivers Efficient Red-Light-Driven PhotocatalysisGraphical AbstractVerified
Journal of Fuel Chemistry and Technology2026

Metal-Free Brush-Like 3D Carbon Nitride Delivers Efficient Red-Light-Driven Photocatalysis

In this study, melamine and cyanuric acid were used as precursors to form supramolecular crystals via hydrogen-bond-assisted self-assembly followed by hydrothermal treatment. Subsequent high-temperature calcination yielded a novel brush-like three-dimensional carbon nitride. The brush-like 3D architecture was found to expose more accessible active sites, markedly accelerate electron transfer, and suppress the recombination of photogenerated charge carriers. The resulting superoxide (O2•−) and hydroxyl (•OH) radicals generated via electron reduction were identified as the key reactive species in the photocatalytic process. Moreover, the surface of the brush-like structure is enriched with nitrogen vacancies, which enhance the catalyst’s ability to harvest visible light. The photocatalytic performance of the brush-like CNS-650 catalyst was evaluated for rhodamine B (RhB) degradation. Under red-light irradiation (660 nm), its degradation rate was 7.4 times higher than that of bulk CN. This work provides valuable insights into the design and application of efficient metal-free 3D photocatalysts.

Read Full Abstract10.1016/S1872-5813(25)60610-4
Intelligent Detection of Drainage Pipeline Defects Based on Cross-Frame Annotation and Recall OptimizationGraphical AbstractVerified
Chinese Journal of Environmental Engineering2026

Intelligent Detection of Drainage Pipeline Defects Based on Cross-Frame Annotation and Recall Optimization

Drainage pipeline defect detection predominantly relies on closed-circuit television (CCTV) inspection, which is labor-intensive, inefficient, and prone to missed detections. Although deep learning-based object detection has been applied, it suffers from low precision, recall, and speed in practical scenarios. This study proposes an engineering-oriented detection scheme achieving high recall and low miss rates. The annotation phase employs a cross-frame strategy combining manual labeling of first and last frames with interpolation and tracking-based refinement. Data preprocessing introduces perceptual hashing to identify similar images, enhancing training efficiency. For detection, a Faster R-CNN model is enhanced with Focal Loss to focus on hard examples, defect classification and grading, and a dynamic threshold strategy to improve recall. Validated on 5,068.72 m of real pipeline data, the method achieves a recall rate exceeding 98% across 16 defect categories, a miss rate of only 2% for grade 4 defects, and a 425% improvement in per-segment detection efficiency compared to manual screening. These results demonstrate the method's effectiveness in balancing recall, miss rate, and speed for engineering deployment.

Read Full Abstract10.12030/j.cjee.202512072
Influence of Preparation Method on the Denitration Performance of Co-Modified Ce/TiO2 CatalystsGraphical AbstractVerified
Journal of Fuel Chemistry and Technology2026

Influence of Preparation Method on the Denitration Performance of Co-Modified Ce/TiO2 Catalysts

This study systematically optimized the preparation of Co-modified Ce/TiO2 catalysts and investigated the effects of preparation method and Co loading on their low-temperature denitrification activity. The sol-gel method with a Co/Ti mass ratio of 0.025 (Ce-Co0.025/TiO2-SG) yielded superior performance compared to impregnation and co-precipitation methods. The catalyst maintained NO conversion above 95% in the 225–350 °C range and exhibited high N2 selectivity. Characterization via BET, XRD, XPS, H2-TPR, and in situ DRIFTS revealed that the enhanced activity was attributed to abundant surface oxygen vacancies, a high proportion of Ce3+ species, and prominent acidic sites. The catalyst followed the Eley-Rideal mechanism, effectively inhibiting nitrate intermediate formation and promoting NO-to-NO2 oxidation. This work provides a reference for developing efficient low-temperature denitrification catalysts for industrial applications such as cement production, which emitted 722,000 tons of NOx in 2020, accounting for 17.3% of industrial emissions.

Read Full Abstract10.1016/S1872-5813(25)60613-X
Rapid Detection of Trace Pb(II) in Water Using a Rod-Shaped Bismuth-Based ElectrodeGraphical AbstractVerified
Chinese Journal of Environmental Engineering2026

Rapid Detection of Trace Pb(II) in Water Using a Rod-Shaped Bismuth-Based Electrode

This study presents a novel electrochemical sensor for the rapid detection of trace lead ions (Pb(II)) in water, utilizing a rod-shaped bismuth-based electrode. The electrode was fabricated by modifying a glassy carbon electrode (GCE) with basic bismuth nitrate [Bi6O5(OH)3](NO3)5·3H2O, synthesized via a chemical precipitation method. The sensor was characterized by X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), electron probe microanalysis (EPMA), and energy-dispersive X-ray spectroscopy (EDS), confirming the rod-like morphology and composition. Electrochemical detection was performed using differential pulse voltammetry (DPV) in a 0.1 mol·L−1 NaAc-HAc buffer (pH 4.3). The sensor exhibited a linear detection range for Pb(II) from 1 to 90 μg·L−1, with a detection limit of 0.34 μg·L−1 and a sensitivity of 106 μA·(μmol·L−1)−1. The electrode demonstrated excellent anti-interference capability and reproducibility. Recovery tests in real water samples (tap water and campus lake water) yielded high recovery rates, indicating practical applicability. This work provides a simple, cost-effective, and reliable method for monitoring trace Pb(II) in environmental water, particularly relevant for public swimming pools and similar aquatic facilities.

Read Full Abstract10.12030/j.cjee.202507057
Exploring the Potential Molecular Mechanisms of Eight Environmental Pollutants in Lung Adenocarcinoma through Network Toxicology, Machine Learning, and Multi-Omics AnalysisGraphical AbstractVerified
Environmental Chemistry2026

Exploring the Potential Molecular Mechanisms of Eight Environmental Pollutants in Lung Adenocarcinoma through Network Toxicology, Machine Learning, and Multi-Omics Analysis

Epidemiological studies have established a significant association between exposure to environmental pollutants (EP) and the risk of lung adenocarcinoma (LUAD). This study integrates network toxicology and multi-omics analysis to elucidate the EP-LUAD molecular regulatory network and identify key regulatory genes, thereby revealing novel mechanisms of environmental carcinogenesis. Transcriptomic data from GEO and TCGA databases yielded 4,971 and 4,488 disease-related targets, respectively. Integration of toxicology databases (TargetNet, Swiss Target Prediction, CTD, SEA) identified 24,860 potential targets for eight common pollutants (SO2, NO, CO, NO2, O3, benzene, toluene, and polycyclic aromatic hydrocarbons). Intersection of these datasets produced 1,536 EP-LUAD common target genes. Protein-protein interaction network analysis identified 247 core targets. Machine learning selected five key genes: AGER, CAV1, CD44, CEP55, and GNB3, which demonstrated robust diagnostic and prognostic efficacy. Their expression correlated with immune cell infiltration, including CD4+ memory T cells and macrophages. Single-cell RNA sequencing revealed epithelial cell-specific expression patterns. Molecular docking confirmed stable pollutant-target binding, with PAH showing highest affinity for CD44 (binding energy −9.32 kcal·mol−1) and GNB3 (−8.32 kcal·mol−1). These findings establish AGER, CAV1, CD44, CEP55, and GNB3 as core molecular mediators of pollution-related LUAD. The high-affinity binding of PAH to CD44 and GNB3 underscores its carcinogenic potential. This study constructs a multi-level regulatory network for EP-LUAD, revealing underlying molecular mechanisms and providing novel potential targets and theoretical basis for early warning and intervention.

Read Full Abstract10.7524/j.issn.0254-6108.2025111002
One-Step Electrodeposition of Cu-Sn Alloy Catalysts for Efficient Electroreduction of CO2 to FormateGraphical AbstractVerified
Journal of Fuel Chemistry and Technology2026

One-Step Electrodeposition of Cu-Sn Alloy Catalysts for Efficient Electroreduction of CO2 to Formate

Electrocatalytic CO2 reduction reaction (CO2RR) offers a promising route to mitigate CO2 emissions while producing valuable chemicals. This study reports a Cu-Sn alloy catalyst with a wheat-ear-like dendritic structure, fabricated via a one-step electrodeposition method, for selective CO2 electroreduction to formate. Compared to pure Cu and Sn electrodes, the Cu-Sn alloy exhibits superior catalytic activity and selectivity toward formate, achieving a maximum Faradaic efficiency (FE) of 80% and maintaining above 70% FE over a potential window from -1.7 V to -2.0 V (vs. Ag/AgCl). The enhanced performance is attributed to the unique dendritic morphology that provides abundant active sites and the synergistic alloying effect that modulates the adsorption of the CO2*- intermediate, as corroborated by electrochemical measurements and X-ray photoelectron spectroscopy (XPS). This work presents a facile strategy for designing bimetallic catalysts for efficient CO2RR to formate.

Read Full Abstract10.3724/2097-213X.2025.JFCT.0027
Effects of Different Functionalized Nanoplastics on the Transformation of Extracellular Antibiotic Resistance Genes in Aquatic EnvironmentsGraphical AbstractVerified
Environmental Chemistry2026

Effects of Different Functionalized Nanoplastics on the Transformation of Extracellular Antibiotic Resistance Genes in Aquatic Environments

The rapid dissemination of antibiotic resistance genes (ARGs) in aquatic environments poses serious threats to public health and environmental safety under the 'One Health' framework. Nanoplastics (NPs), as co-occurring pollutants, can exacerbate ARG risks by promoting horizontal gene transfer (HGT), yet the influence of different functional groups on extracellular ARG (eARG) transformation remains unclear. This study investigated the effects of carboxy-modified polystyrene NPs (PS-COOH) and amino-functionalized polystyrene NPs (PS-NH2) compared to unmodified polystyrene NPs (PS) on the transformation of the extracellular resistance plasmid IE-V1955 (carrying an ampicillin resistance gene) into Escherichia coli DH5α. Results showed that PS-COOH exposure promoted plasmid transformation similarly to PS, with effects increasing over 0.1–20 mg·L−1. Low concentrations (0.1–0.5 mg·L−1) of PS-NH2 also enhanced transformation, with stronger effects than PS-COOH at equal doses, whereas high concentrations (1–20 mg·L−1) inhibited it. Mechanistically, PS-COOH (0.1–20 mg·L−1) and low PS-NH2 induced intracellular reactive oxygen species (ROS), increased cell membrane permeability, elevated the protein-to-polysaccharide ratio in extracellular polymeric substances (EPS), and promoted biofilm formation, thereby facilitating transformation. High PS-NH2 concentrations caused excessive ROS leading to cell lysis and formed aggregates with plasmids larger than membrane pores, blocking uptake. These findings provide a theoretical basis for assessing the combined environmental health risks of NPs and ARGs.

Read Full Abstract10.7524/j.issn.0254-6108.2024112804
Molecular Dataset of Paraffin Oxidative Pyrolysis: ReaxFF Molecular Dynamics Simulations and Reaction Network AnalysisGraphical AbstractVerified
Journal of Fuel Chemistry and Technology2026

Molecular Dataset of Paraffin Oxidative Pyrolysis: ReaxFF Molecular Dynamics Simulations and Reaction Network Analysis

This dataset provides high-precision molecular dynamics trajectories for oxidative pyrolysis of three paraffin models with distinct straight-chain hydrocarbon distributions, simulated over a temperature range of 2100–2500 K. The COMPASS force field was used for initial structure optimization, and the ReaxFF reactive force field for pyrolysis simulation. The database comprises atomic trajectories, species evolution information, and reaction network analysis results for both heating and isothermal cracking processes, totaling approximately 141 GB and including 150,000 atomic configuration frames. Data are stored in a hierarchical directory structure, supporting multi-scale mechanistic studies. The dataset enables quantitative analysis of carbon chain length effects on reaction pathways, high-resolution tracking of free radical evolution, and extraction of kinetic parameters across a wide temperature range. It provides an atomic-scale foundation for understanding paraffin oxidative pyrolysis, with implications for addressing wax deposition in oil and gas extraction, enhancing product selectivity in cracking processes, and advancing clean fuel technologies. The data are publicly available via DOI:10.57760/sciencedb.31639.

Read Full Abstract10.1016/S1872-5813(26)60646-9
Cardiovascular Toxicity Induced by Micro/Nano-Plastics and Its MechanismsGraphical AbstractVerified
Environmental Chemistry2026

Cardiovascular Toxicity Induced by Micro/Nano-Plastics and Its Mechanisms

Micro/nano-plastics (MNPs) are emerging contaminants widely detected in human circulatory systems, including blood, heart, and vascular endothelium, raising concerns about cardiovascular health risks. This systematic review analyzed 61 peer-reviewed studies (2008–2024) to elucidate the cardiotoxic effects and molecular mechanisms of MNPs. Evidence indicates that MNPs exposure elevates risks of atherosclerosis, thrombosis, and arrhythmias through oxidative stress, inflammatory cascades, endothelial dysfunction, and metabolic dysregulation. Notably, co-exposure with persistent organic pollutants (POPs) or heavy metals may produce synergistic or antagonistic effects. Current research relies predominantly on animal and cell models, with critical gaps in low-dose, long-term exposure data and epidemiological evidence. Future studies should optimize experimental designs, integrate metabolomics and epigenetics, and explore transgenerational effects and combined toxicity mechanisms to inform pollution control policies and mitigate cardiovascular risks.

Read Full Abstract10.7524/j.issn.0254-6108.2025073004
Catalytic Reforming of Lignite Pyrolysis Volatiles over Metal Oxide and Zeolite Tandem Catalysts for Light Aromatics ProductionGraphical AbstractVerified
Journal of Fuel Chemistry and Technology2026

Catalytic Reforming of Lignite Pyrolysis Volatiles over Metal Oxide and Zeolite Tandem Catalysts for Light Aromatics Production

Pyrolysis is a key route for the graded conversion of low-rank coal, yet the volatiles are rich in oxygenates and heavy components, limiting direct utilization. This study proposes a tandem catalytic system combining metal oxides and ZSM-5 zeolite to efficiently convert lignite pyrolysis volatiles into light aromatics (benzene, toluene, ethylbenzene, xylene, naphthalene, methylnaphthalene). The upper-layer metal oxide pre-cracks large molecules and removes oxygenates, reducing carbon deposition on the zeolite and extending catalyst life. Among metal oxides tested, strongly basic MgO exhibited superior cracking and deoxygenation performance. Compared to ZSM-5 alone, the MgO/ZSM-5 tandem system increased total light aromatics yield by approximately 20% to 21.5 mg/g, while maintaining liquid product proportion at 21.4%. The incorporation of MgO also significantly reduced coke deposition on ZSM-5, preserving its catalytic activity and potentially prolonging its operational lifespan. These findings provide a theoretical basis for upgrading low-rank coal pyrolysis volatiles to valuable light aromatics.

Read Full Abstract10.3724/2097-213X.2025.JFCT.0028
Body Burden of Polybrominated Diphenyl Ethers and Joint Effects on Thyroid Function in a Physical Examination Population in ShenzhenGraphical AbstractVerified
Environmental Chemistry2026

Body Burden of Polybrominated Diphenyl Ethers and Joint Effects on Thyroid Function in a Physical Examination Population in Shenzhen

This study characterized the body burden of polybrominated diphenyl ethers (PBDEs) in a physical examination population in Shenzhen and evaluated its impact on thyroid function. Serum samples from 368 residents were analyzed for eight PBDE congeners using atmospheric pressure gas chromatography-tandem mass spectrometry (APGC-MS/MS). The median concentration of ∑8PBDEs was 10.2 ng·g⁻¹ lipid weight (lw), ranging from 0.13 to 2089.4 ng·g⁻¹ lw, with BDE-209 predominating (59.7% of total). Multiple linear regression revealed that a 1.7-fold increase in serum BDE-153 was associated with a 0.4% increase in free triiodothyronine (FT3) (P<0.05), while a 1.7-fold increase in BDE-183 was associated with a 0.9% decrease in total triiodothyronine (T3) and a 0.7% decrease in FT3 (P<0.05). Bayesian kernel machine regression (BKMR) indicated a negative correlation between mixed PBDE exposure and thyroid-stimulating hormone (TSH) at high exposure levels. Weighted quantile sum (WQS) regression showed that mixed exposure was associated with decreased T3 levels and T3/FT3 ratio, with BDE-153 and BDE-183 as the primary contributors. These findings suggest that PBDE exposure may adversely affect thyroid function and disrupt thyroid hormone homeostasis, with BDE-183 and BDE-153 playing key roles. This study provides a scientific basis for PBDE health risk assessment and thyroid protection.

Read Full Abstract10.7524/j.issn.0254-6108.2025121602
Mechanisms of Natural Organic Matter in Regulating Microplastic Aggregation and Transport in Soil-Groundwater Systems: A ReviewGraphical AbstractVerified
Environmental Chemistry2026

Mechanisms of Natural Organic Matter in Regulating Microplastic Aggregation and Transport in Soil-Groundwater Systems: A Review

Microplastics (MPs) are persistent emerging contaminants ubiquitously distributed in soil-groundwater environments, where their aggregation and transport critically govern pollutant fate and ecological risks. Natural organic matter (NOM), a complex assemblage of organic compounds, interacts with MPs and porous media via hydrogen bonding, π-π interactions, hydrophobic effects, and electrostatic binding, thereby modulating MP surface properties and environmental behavior. This review systematically synthesizes the mechanisms by which NOM influences MP aggregation and transport, with emphasis on the distinct roles of humic substances, proteins, and extracellular polymeric substances (EPS), and their synergistic modulation with solution chemistry (pH, ionic strength, ion type). Additionally, NOM accelerates MP aging and alters surface characteristics, consequently impacting transport capacity. Current research limitations are identified, and future directions are proposed to inform MP pollution risk assessment and management strategies. Key findings indicate that NOM generally enhances MP stability and mobility at low ionic strengths, while high ionic strengths may induce aggregation depending on NOM type and ion valence. Humic substances predominantly increase electrostatic repulsion, whereas proteins and EPS can bridge particles, promoting aggregation. Aging processes, accelerated by NOM photochemical activity, increase surface oxygen functionality and hydrophilicity, further altering transport. The review underscores the need for systematic studies under environmentally relevant conditions to predict MP fate accurately.

Read Full Abstract10.7524/j.issn.0254-6108.2024112806
Neurotoxicity of Carboxyl-Modified Polystyrene Microplastics on Zebrafish at Early Developmental StageGraphical AbstractVerified
Environmental Chemistry2026

Neurotoxicity of Carboxyl-Modified Polystyrene Microplastics on Zebrafish at Early Developmental Stage

Carboxyl-modified polystyrene microplastics (PS-COOH) are negatively charged particles formed by surface oxidation and functional group modification of polystyrene microplastics (PS), widely used in biomedical and analytical chemistry. However, studies on their neurotoxic effects on aquatic organisms are scarce. This study employed zebrafish (Danio rerio) as a model organism, exposing embryos to environmentally relevant concentrations (0.1, 1, 10, 100 μg·L−1) of PS and PS-COOH. Neurotoxic effects were assessed by measuring tail coiling frequency at 24 hpf and swimming velocity under alternating light/dark cycles at 120 hpf. Results demonstrated that both PS and PS-COOH induced neurotoxicity, with PS-COOH significantly reducing tail coiling frequency and average swimming speed compared to PS (P<0.05). Exposure to 10 μg·L−1 PS-COOH disrupted neurotransmitter homeostasis, altering levels of acetylcholine (ACh), serotonin (5-HT), and γ-aminobutyric acid (GABA). Transgenic zebrafish Tg(huc:EGFP) fluorescence assays revealed that PS-COOH (0.1–100 μg·L−1) caused damage to central neurons. These findings indicate that PS-COOH exposure impairs cholinergic, serotonergic, and GABAergic neurotransmission, induces neuronal damage, and exerts neurotoxic effects on zebrafish larvae. This study provides a theoretical basis for assessing the ecological and health risks of modified microplastics.

Read Full Abstract10.7524/j.issn.0254-6108.2024112104
Determination of Per- and Polyfluoroalkyl Substances in Vegetables by Solid-Phase Extraction Combined with Ultra-High Performance Liquid Chromatography-Tandem Mass SpectrometryGraphical AbstractVerified
Environmental Chemistry2026

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

Vegetable consumption is a well-established pathway for human exposure to per- and polyfluoroalkyl substances (PFAS). These contaminants are absorbed by vegetables through uptake from soil and irrigation water, leading to bioaccumulation within plant tissues and posing potential risks to human health. Therefore, monitoring PFAS concentrations in vegetables is critical for assessing dietary exposure and associated health risks. In this study, a solid-phase extraction (SPE) followed by ultra-high performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method was developed for the determination of 24 PFAS compounds in leafy vegetables, including Shanghai Bok Choy, Cabbage, and Water Spinach. The analytical method, incorporating organic solvent extraction followed by SPE cleanup, was optimized with respect to both extraction solvent and SPE sorbent. Alkaline methanol was used as the extraction solvent, and PFAS in vegetables were extracted via vortex-assisted extraction. Tandem mass spectrometry was used for detection in multiple reaction monitoring mode, and quantification was performed by internal standard method. Under optimized conditions, at a spiking level of 2 ng, recoveries ranged from 50.0% to 120.8% with relative standard deviations (RSD) between 1.0% and 26%. Calibration curves showed good linearity with correlation coefficients (r) greater than 0.99. Limits of detection (LOD, S/N=3) were between 0.002 and 0.103 ng·g−1, and limits of quantification (LOQ, S/N=10) were between 0.007 and 0.343 ng·g−1. The method was applied to real samples, detecting 20 PFAS, with 10 compounds showing 100% detection frequency. Total PFAS concentrations ranged from 2.92 to 6.83 ng·g−1 dry weight (dw). Perfluorobutanoic acid (PFBA) was the dominant contaminant, with concentrations from 1.18 to 3.74 ng·g−1 dw. The method demonstrates good sensitivity and accuracy, effectively identifying and quantifying multiple PFAS, thus providing reliable technical support for monitoring PFAS in vegetables.

Read Full Abstract10.7524/j.issn.0254-6108.2025010402