SinoGreenTech Academic Portal
📚 Peer-Reviewed Translated Literature

All Clean Energy & Battery Intelligence (Page 30)

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 1498 peer-reviewed translated articles (Page 30 of 63)

Rapid Granulation of Anaerobic Sludge in Methanol Wastewater Treatment Using Functional AdditivesGraphical AbstractVerified
Chinese Journal of Environmental Engineering2026

Rapid Granulation of Anaerobic Sludge in Methanol Wastewater Treatment Using Functional Additives

Methanol is highly biodegradable, yet its efficient and stable anaerobic treatment is constrained by prolonged microbial adaptation to toxic substances, narrow microbial community structure, and poor sludge granulation. This study applied two functional additives—sodium bicarbonate (NaHCO3) as an inorganic carbon source (IC) and an amino-acid-rich organic functional supplement (FS)—to accelerate the startup of two upflow anaerobic sludge blanket (UASB) reactors. UASB-A received 3,000 mg·L−1 NaHCO3 and 127 mg·L−1 FS, while UASB-B received only 3,000 mg·L−1 NaHCO3. Both additives enabled rapid startup and granulation by shortening hydraulic retention time (HRT) and increasing organic loading rates (4, 6, 9, 15, 20, and 30 g COD·L−1·d−1). Granulation was evidenced by increased total suspended solids (TSS), volatile suspended solids (VSS), and particle size distribution. Microbial community analysis at HRT 0.2 d revealed highest relative abundances of Acetobacterium at 30.2% (UASB-A) and 36.9% (UASB-B). NaHCO3 supplementation enhanced syntrophy between Acetobacterium and the acetoclastic methanogen Methanothrix, while FS significantly increased the abundance of Sporomusa, establishing a novel syntrophic relationship with Methanothrix. These interactions promoted sludge granulation. The study demonstrates that functional additives facilitate rapid startup and granulation in methanol anaerobic treatment, offering a strategy to overcome process bottlenecks.

Read Full Abstract10.12030/j.cjee.202507088
Water Quality Trend Analysis of the Sanshenggong Section of the Yellow River from 2011 to 2024 Based on Mann-Kendall Test and Fuzzy Comprehensive EvaluationGraphical AbstractVerified
Chinese Journal of Environmental Engineering2026

Water Quality Trend Analysis of the Sanshenggong Section of the Yellow River from 2011 to 2024 Based on Mann-Kendall Test and Fuzzy Comprehensive Evaluation

The Sanshenggong section of the Yellow River is a critical hydrological monitoring and control point, whose water quality directly affects the ecological safety and sustainable water resource utilization of the middle and lower reaches. This study analyzed water quality monitoring data from 2011 to 2024 using the Mann-Kendall test to identify abrupt change years, combined with single-factor evaluation and a fuzzy comprehensive evaluation method improved by CRITIC-entropy weight combination to systematically assess water quality evolution. The Mann-Kendall test identified 2013 and 2019 as abrupt change points, with non-significant improvement from 2013 to 2015 and significant improvement after 2016. Single-factor evaluation indicated that total phosphorus (TP) was the primary exceeding factor in 2011–2012, and its declining concentration drove the water quality upgrade from Class III to Class II in 2013. The CRITIC-entropy weight combination assigned the highest weight (28.96%) to permanganate index, whose decline was the core driver of water quality improvement. The improved fuzzy evaluation showed that the membership degree of Class III water dropped to zero in 2013, indicating stable improvement, but periodic rebounds in Class II membership suggested potential degradation risks. This study provides scientific evidence for ecological protection and high-quality development of the Yellow River Basin.

Read Full Abstract10.12030/j.cjee.202508013
Analysis of Treatment and Resource Utilization of Coal Chemical Waste Salt: Current Status and ProspectsGraphical AbstractVerified
Chinese Journal of Environmental Engineering2026

Analysis of Treatment and Resource Utilization of Coal Chemical Waste Salt: Current Status and Prospects

Coal chemical waste salt, a solid residue from evaporative crystallization of high-salinity wastewater, poses significant environmental risks and challenges for resource utilization due to its complex composition. This study systematically analyzes its composition and environmental hazards, highlighting its typical "mixed salt" nature and the potential threats of organic pollutants and heavy metals to soil, water, and ecosystems. It reviews mainstream treatment pathways, including organic degradation, inorganic impurity removal, and salt separation, with a focus on the resource utilization of sodium chloride and sodium sulfate and their industrial prospects. The current pollution control technical specifications and product quality standards are examined, comparing the scope and technical points of relevant standards such as the "Technical Specification for Pollution Control of Chemical Waste Salt." Finally, countermeasures are proposed to address challenges including difficult treatment of mixed salts, insufficient resource utilization incentives, and incomplete standard systems, emphasizing technological innovation, policy guidance, and standard improvement.

Read Full Abstract10.12030/j.cjee.202507081
Removal Mechanisms of Fe3O4@MIL-100(Fe) for Microplastics in WaterGraphical AbstractVerified
Chinese Journal of Environmental Engineering2026

Removal Mechanisms of Fe3O4@MIL-100(Fe) for Microplastics in Water

Microplastics (MPs) are frequently detected in various water bodies, posing increasing environmental risks. This study synthesized magnetic Fe3O4@MIL-100(Fe) microspheres via an in-situ one-step hydrothermal method and investigated their adsorption removal mechanisms for polystyrene (PS) and polylactic acid (PLA) microplastics. The composite exhibited a core-shell structure with a high specific surface area of 848.6 m2·g−1. Adsorption kinetics showed that PLA followed a pseudo-second-order model, while PS fitted both pseudo-first-order and pseudo-second-order models. Equilibrium data for both MPs were well described by the Freundlich isotherm. Removal efficiencies for PLA and PS increased from 58.18% and 49.66% to 98.90% and 98.58%, respectively, as pH decreased, and from 64.24% and 21.58% to 97.05% and 94.63% with increasing ionic strength. The removal mechanism involved synergistic physical-chemical interactions: hydrogen bonding dominated for PLA, with some complexation, while π–π interactions and hydrogen bonding were primary for PS. The material demonstrated excellent reusability over multiple cycles. These findings highlight the potential of Fe3O4@MIL-100(Fe) for efficient removal of MPs from water, offering a novel approach for controlling emerging contaminants.

Read Full Abstract10.12030/j.cjee.202510089
A Novel Continuous-Flow Self-Circulating Upflow Granular Sludge Bed Process for Treating Real Domestic WastewaterGraphical AbstractVerified
Chinese Journal of Environmental Engineering2026

A Novel Continuous-Flow Self-Circulating Upflow Granular Sludge Bed Process for Treating Real Domestic Wastewater

Aerobic granular sludge (AGS) is an economical and efficient technology, yet its application has been largely confined to sequencing batch reactors (SBRs). This study introduces a novel continuous-flow self-circulating upflow granular sludge bed (Zier) process with separate aeration for treating real domestic wastewater. By regulating operational parameters, the nitrogen removal performance and granular sludge stability were investigated. Under hydraulic retention time of 10 h, self-circulation times of 29–58, and upflow velocity of 11–18 m·h−1, effluent NH4+-N and TN averaged (5±3.4) mg·L−1 and (10±2.8) mg·L−1, respectively, with COD at (30±6.2) mg·L−1. The process maintained sludge stability: mixed liquor suspended solids increased from 5,080 to 6,650 mg·L−1, mean particle size was 209.6 μm, and sludge volume index (SVI) remained at 50–60 mL·g−1. Extracellular polymeric substances (EPS) increased from 26.05 to 68.27 mg·g−1, with proteins (PN) rising from 21.26 to 59.44 mg·g−1 and polysaccharides (PS) from 4.79 to 8.82 mg·g−1, elevating the PN/PS ratio from 4.4 to 6.7. These results confirm that the Zier process preserves granular structure and function in continuous flow. The process demonstrates robust nitrogen removal and offers a novel approach for continuous-flow AGS applications in real wastewater treatment.

Read Full Abstract10.12030/j.cjee.202509035
Optimization of Preparation Conditions for a Novel Composite Slow-Release Carbon Source and Its Denitrification PerformanceGraphical AbstractVerified
Chinese Journal of Environmental Engineering2026

Optimization of Preparation Conditions for a Novel Composite Slow-Release Carbon Source and Its Denitrification Performance

To address the issues of insufficient carbon sources and low denitrification efficiency in rural domestic wastewater, this study developed and optimized a composite slow-release carbon source using corncob, rice husk, reed straw, polyvinyl alcohol (PVA), and sodium alginate (SA). The preparation conditions and raw material ratios were systematically optimized using Plackett-Burman (PB) design, response surface methodology (Box-Behnken design, BBD), and mixture-optimal design (MOD). The denitrification performance was evaluated through carbon release characteristics and denitrification experiments. The optimal preparation conditions were determined as PVA 8.64 g, SA 2.41 g, rice husk 3.82 g, corncob 4.47 g, reed straw 6.06 g, freezing time 19.11 h, and crosslinking time 12 h. The 7-day cumulative carbon release was (43.38 ± 1.3) mg·(g·h)−1. The release process followed first-order kinetics, Higuchi, Ritger-Peppas, and Weibull models, indicating that carbon release is controlled by multiple mechanisms including diffusion and skeleton erosion, ensuring stable slow-release characteristics. In denitrification experiments with influent NO3−-N concentration of 50 mg·L−1, the composite carbon source (RCR-PVA-SA) achieved a maximum NO3−-N removal rate of 90.8% after 10 days of operation, with a removal rate of 0.079 mg·(g·h)−1. Under dynamic conditions with hydraulic retention time (HRT) of 3 h, the average removal rate remained at 87.9%, demonstrating efficient and stable denitrification performance under both static and dynamic conditions. This research provides a reference for the preparation of natural slow-release carbon sources and the resource utilization of agricultural waste.

Read Full Abstract10.12030/j.cjee.202508036
Removal of Pollutants from Urban Surface Runoff by a Straw-Based Composite Bioretention SystemGraphical AbstractVerified
Chinese Journal of Environmental Engineering2026

Removal of Pollutants from Urban Surface Runoff by a Straw-Based Composite Bioretention System

Surface runoff pollution has become a significant source of water contamination. This study constructed an integrated composite bioretention system comprising straw, aquatic plant, and biochar zones for purifying urban surface runoff, aiming to meet the standards for reuse as landscaping water. The system's performance in removing conventional pollutants and polycyclic aromatic hydrocarbons (PAHs) was investigated, along with microbial community structure analysis. Results showed removal efficiencies of 81.1% for COD, 98.1% for TN, 79.1% for TP, and 90.3% for TSS, with effluent meeting the 'Water Quality for Scenic and Recreational Use' (GB/T 18921-2019) standard. The system exhibited robust resistance to pollutant and hydraulic loading. The alkali-modified straw zone was the primary pollutant removal region, facilitating physical adsorption and capture of suspended solids, while released carbon sources enhanced total nitrogen removal. This zone exhibited the highest microbial richness, with relative abundances of Proteobacteria and Firmicutes at 54.3% and 21.9%, respectively. The system effectively removed all 16 priority PAHs, reducing effluent toxicity equivalent by 86.5%. The straw zone completely removed four high-molecular-weight PAHs (BaP, DahA, BghiP, IcdP), while aquatic plants and biochar effectively removed medium- and low-molecular-weight PAHs.

Read Full Abstract10.12030/j.cjee.202410085
Multidimensional Groundwater Quality Assessment and Source Apportionment in the Guyuan Region, NingxiaGraphical AbstractVerified
Chinese Journal of Environmental Engineering2026

Multidimensional Groundwater Quality Assessment and Source Apportionment in the Guyuan Region, Ningxia

Groundwater is a vital drinking and irrigation source in the loess regions of northwestern China. In Guyuan, a densely populated area in southern Ningxia, systematic assessments of groundwater pollution risks are lacking. This study collected 60 groundwater samples and employed the Nemerow index, heavy metal pollution index (HPI), and health risk assessment models to evaluate pollution levels and health risks of eight elements including Cr, As, and Hg. Results show that the groundwater is generally Class IV quality, with a mean TDS of 1350.9 mg·L−1. Average concentrations of As, Cr, and Mn are 4.39, 29.87, and 45.77 μg·L−1, respectively. The Nemerow index indicates moderate pollution. The mean HPI is 10.56, but a local sample (PS1-51-下) reaches 36.15, indicating severe pollution. Health risk assessment reveals that carcinogenic risks from Cr and As for adults and children are 8.037×10−6 a−1 and 3.863×10−6 a−1, respectively, below US EPA limits but above recommended levels by Swedish and Dutch agencies, with children at higher risk. Hydrogen and oxygen isotopes and principal component analysis suggest that groundwater is primarily recharged by atmospheric precipitation. Cr, Zn, and Mn mainly originate from regional copper ore belts, coal mining, and agricultural activities. This study fills a gap in multidimensional groundwater assessment in populated loess areas, identifies pollution characteristics distinct from typical loess regions, and provides a scientific basis for regional water resource risk management and sustainable development.

Read Full Abstract10.12030/j.cjee.202506084
Biosurfactant-Enhanced Electrokinetic-Biobarrier Remediation of Polycyclic Aromatic Hydrocarbon-Contaminated Soil from an Industrial SiteGraphical AbstractVerified
Chinese Journal of Environmental Engineering2026

Biosurfactant-Enhanced Electrokinetic-Biobarrier Remediation of Polycyclic Aromatic Hydrocarbon-Contaminated Soil from an Industrial Site

Polycyclic aromatic hydrocarbons (PAHs) in industrial soils pose significant risks due to their hydrophobicity and low bioavailability, limiting the efficacy of bioremediation. This study investigated the enhancement of an in-situ electrokinetic-biological barrier (EK-BB) system for PAH-contaminated soil using biosurfactants. Three biosurfactants—rhamnolipid (RL), alkyl polyglycoside (APG), and saponin (SAP)—were applied individually and in combinations at 10× critical micelle concentration (CMC), and the optimal RL+APG mixture was further tested at 2.5, 5.0, 7.5, and 10× CMC. Results showed that biosurfactant application improved soil electrical current, moisture retention, and PAH removal. Combined surfactants outperformed single ones, with the 10× CMC RL+APG treatment (Exp IV) achieving the highest average current intensity and moisture content, 1.31 and 1.12 times that of the control (CK), respectively, and a PAH removal of 106.02 mg·kg⁻¹. Biosurfactants also promoted bacterial growth in both contaminated soil and the biobarrier layer; the 10× CMC RL+APG treatment increased bacterial counts by 6.24-fold and 44.8%, respectively. However, excessive surfactant concentrations led to PAH accumulation in the biobarrier and clean soil. The 5× CMC RL+APG treatment provided optimal balance, maximizing PAH removal while maintaining barrier effectiveness. These findings confirm that appropriate biosurfactant concentrations can enhance EK-BB remediation, offering technical support for PAH-contaminated site remediation and safe reuse.

Read Full Abstract10.12030/j.cjee.202508053
Mechanical Properties and Microstructural Evolution of CO2-Mineralized Cured Steel Slag-Fly Ash Composite Cementitious MaterialsGraphical AbstractVerified
Chinese Journal of Environmental Engineering2026

Mechanical Properties and Microstructural Evolution of CO2-Mineralized Cured Steel Slag-Fly Ash Composite Cementitious Materials

This study investigates the optimization of CO2 mineralization curing on the performance of a ternary cementitious system comprising steel slag, fly ash, and Portland cement. Specimens were fabricated with varying residual water-to-cement ratios (r/w), steel slag and fly ash contents, curing pressures, and durations, then subjected to standard curing and CO2 mineralization curing. Compressive strength and carbon sequestration rate were measured, and X-ray diffraction (XRD) and scanning electron microscopy (SEM) were employed to analyze mineral composition and microstructural evolution. Results indicate that compressive strength first increases then rapidly decreases with increasing residual water-to-cement ratio, with an optimal r/w below 0.15. Both compressive strength and carbon sequestration rate increase with higher steel slag content; the 50% steel slag + 10% fly ash formulation exhibited the highest values. Microstructural analyses revealed that CO2 mineralization primarily consumes hydration products such as Ca(OH)2, C-S(Al)-H, and AFt, generating abundant calcium carbonate that densifies the pore structure, thereby enhancing mechanical properties. Lower residual water-to-cement ratios, higher steel slag content, or extended curing durations increase the content and crystallinity of calcium carbonate. SEM observations confirmed the presence of densely packed, well-crystallized rhombohedral calcite in specimens with lower water-to-cement ratios and higher steel slag content. These findings provide a mechanistic basis for the engineering application of CO2 mineralization curing in ternary solid-waste cementitious materials.

Read Full Abstract10.12030/j.cjee.202507095
Stress Responses and Accumulation Characteristics of Duckweed (Landoltia punctata) to Lead Oxide NanoparticlesGraphical AbstractVerified
Chinese Journal of Environmental Engineering2026

Stress Responses and Accumulation Characteristics of Duckweed (Landoltia punctata) to Lead Oxide Nanoparticles

Lead oxide nanoparticles (PbO NPs) are increasingly released into aquatic environments from industrial processes, posing ecological risks. Duckweed (Landoltia punctata) is a known lead hyperaccumulator, but its physiological and biochemical responses to PbO NPs remain unexplored. This study synthesized PbO NPs via a plant-mediated biosynthesis method and exposed L. punctata to concentrations of 0 (control), 10, 20, 30, and 40 mg·L−1 in hydroponic culture for 7 days. Results showed concentration-dependent effects: low concentrations (10–20 mg·L−1) stimulated growth, while high concentrations (≥30 mg·L−1) inhibited fresh weight, growth rate, and root length. Chlorophyll b content decreased significantly at ≥20 mg·L−1 (by 14.09%, 10.79%, and 18.48% at 20, 30, and 40 mg·L−1, respectively), while carotenoid content increased. Malondialdehyde content and activities of superoxide dismutase, peroxidase, and catalase increased with PbO NPs concentration, indicating oxidative stress. Lead accumulation reached 1265.65 mg·kg−1 at 30 mg·L−1 and 2030.01 mg·kg−1 at 40 mg·L−1, with bioconcentration factors >1 and lead removal rates above 68.94%. Subcellular distribution showed lead predominantly in the cell wall fraction, followed by soluble components and organelles. These findings demonstrate that L. punctata exhibits strong PbO NPs accumulation and stress tolerance, supporting its use in phytoremediation of metal nanoparticle-contaminated waters.

Read Full Abstract10.12030/j.cjee.202508041
Characterization of Pollutants in Coal Chemical Industry Waste Salt and Its Resource Utilization Potential: A Case Study of a Coal Chemical Industrial Park in Northwest ChinaGraphical AbstractVerified
Chinese Journal of Environmental Engineering2026

Characterization of Pollutants in Coal Chemical Industry Waste Salt and Its Resource Utilization Potential: A Case Study of a Coal Chemical Industrial Park in Northwest China

Coal chemical industry waste salt, generated from high-salinity wastewater treatment, poses a bottleneck for green transformation under the 'dual carbon' strategy due to its low value and high complexity. This study investigated a typical coal chemical industrial park in Northwest China, using principal component analysis (PCA) on actual waste salt samples to identify pollutant characteristics and assess resource utilization potential. Results showed total organic carbon (TOC) ranged from 707.9 to 7,737.9 mg·kg⁻¹, with benzo(a)pyrene concentrations frequently exceeding the limits of the 'Identification Standards for Hazardous Wastes' (GB 5085.3). Hardness ions and metal ions also surpassed relevant product standards. PCA classified the waste salts into three types: sodium sulfate type, sodium chloride type, and high-complexity mixed salt, each corresponding to distinct resource utilization pathways. The study proposes differentiated technical routes based on PCA classification, providing a feasible reference for classified management and technology selection. This research supports the national policy of 'harmless pretreatment + resource utilization' for waste salt, contributing to green and high-quality development of the coal chemical industry.

Read Full Abstract10.12030/j.cjee.202508021
Spatial Differentiation of Heavy Metals in a Landfill Site in a High-Altitude Cold Region Driven by Freeze-Thaw CyclesGraphical AbstractVerified
Chinese Journal of Environmental Engineering2026

Spatial Differentiation of Heavy Metals in a Landfill Site in a High-Altitude Cold Region Driven by Freeze-Thaw Cycles

This study investigated the spatial distribution and ecological risk of heavy metals (As, Cd, Cr, Cu, Ni, Pb, Zn) in soil beneath an informal waste dump in a pastoral area of Baingoin County, Nagqu City, Tibet, a high-altitude cold region with frequent freeze-thaw cycles. A total of 55 soil samples were collected from surface (0 cm), middle (10-30 cm), and deep (50 cm) layers. Single-factor index (Pi), geo-accumulation index (Igeo), Nemerow index (PN), and risk assessment code (RAC) were employed to evaluate contamination levels and potential ecological risks, while Kriging interpolation was used to map spatial distribution. Results showed that average concentrations of all seven heavy metals exceeded local background values. Horizontally, high-concentration zones were mainly located at five points within the dump. Vertically, Cd, Cu, Pb, and Zn were significantly enriched in the surface layer, whereas Ni exhibited higher concentrations in deeper layers, indicating downward migration driven by freeze-thaw processes. All evaluation methods identified Cd as the primary pollutant. Speciation analysis revealed that heavy metals were predominantly in the residual fraction, with Ni having the highest weak-acid-extractable fraction (5.55%), indicating strong mobility and potential biological toxicity. This study fills a gap in systematic research on informal waste dumps in high-altitude ecologically fragile areas and provides a case reference for environmental management and remediation of such sites in cold regions.

Read Full Abstract10.12030/j.cjee.202508050
Strength and Microstructural Characteristics of Sludge Solidified by Loess-Based Composite Solidifying AgentGraphical AbstractVerified
Chinese Journal of Environmental Engineering2026

Strength and Microstructural Characteristics of Sludge Solidified by Loess-Based Composite Solidifying Agent

To address land waste and poor bearing capacity from sludge landfill, this study developed a composite solidifying agent using loess, fly ash, desulfurized gypsum, and cement. Orthogonal experiments combined strength testing, SEM/XRD microanalysis, permeability and heavy metal leaching tests, and cost accounting. Results show that cement significantly enhances early and mid-term strength, while loess dominates later strength development. Optimal fly ash and desulfurized gypsum content is 12% each. The optimal mix ratio (loess:fly ash:desulfurized gypsum:cement:sludge) is 0.1:0.12:0.12:0.08:1. The solidified matrix forms dense structures via C-S-H gel and ettringite (Aft), effectively controlling heavy metal leaching at low cost. This work enables solid waste resource utilization and provides robust support for sludge solidification engineering.

Read Full Abstract10.12030/j.cjee.202507094
Multi-stage Activation of Fly Ash for Al(OH)3 Extraction: Process Optimization and Mechanistic InsightsGraphical AbstractVerified
Chinese Journal of Environmental Engineering2026

Multi-stage Activation of Fly Ash for Al(OH)3 Extraction: Process Optimization and Mechanistic Insights

Selective recovery of aluminum compounds from fly ash is a key route for its high-value utilization. This study developed a multi-stage activation process for extracting Al(OH)3 from fly ash, comprising mechanical activation, calcination activation, chemical separation, and carbonation precipitation. Fly ash was mixed with carbide slag and CaF2, then calcined; the resulting clinker was leached with Na2CO3 solution to extract Al. The CaO generated from high-temperature calcination of carbide slag facilitated the separation of Si and Al. After solid-liquid separation, CO2 was introduced into the Al-rich leachate to precipitate Al(OH)3. The process promoted the formation of Ca12Al14O32F2 and inert Ca2SiO4, achieving efficient Si-Al separation during calcination. Under optimal conditions (mechanical activation for 60 min, 4% CaF2, calcination at 1000°C for 2 h, leaching with 40 g/L Na2CO3), the Al extraction rate reached 91.8%, and the product purity was 98.9%. The alumina extraction residue exhibited porous and highly reactive characteristics, suitable for producing flame-retardant materials or high-value silicon-based products (e.g., white carbon black, molecular sieve adsorbents). The process offers a promising industrial route for fly ash valorization, with potential integration with cement production lines for synergistic CO2 capture and utilization.

Read Full Abstract10.12030/j.cjee.202508047
Interface Regulation for Enhanced Photoelectrochemical Performance of CuBi2O4 PhotocathodesGraphical AbstractVerified
Journal of Fuel Chemistry and Technology2026

Interface Regulation for Enhanced Photoelectrochemical Performance of CuBi2O4 Photocathodes

Photoelectrochemical (PEC) water splitting offers a direct route to convert solar energy into clean hydrogen fuel. CuBi2O4, a p-type semiconductor with a bandgap of 1.5–1.8 eV, exhibits visible-light responsiveness and good stability, yet its performance is limited by high interfacial resistance and severe charge carrier recombination. This study introduces a CuO interlayer between fluorine-doped tin oxide (FTO) and CuBi2O4 to construct CuO/CuBi2O4 photocathodes, aiming to improve interfacial charge transfer. The optimized CuO/CuBi2O4-200 photocathode achieved a photocurrent density of −1.71 mA/cm² at 0 V vs. RHE, more than 3.5 times that of bare CuBi2O4. Incident photon-to-current efficiency (IPCE) at 365 nm reached ~13%, and the maximum applied bias photon-to-current efficiency (ABPE) was 0.17%. Water splitting experiments yielded 2.05 μmol/cm² of hydrogen, significantly surpassing the unmodified photoelectrode. Mechanistic studies indicate that the CuO layer establishes favorable band alignment, promotes hole transport toward the FTO substrate, and suppresses interfacial carrier recombination. This work demonstrates a simple and efficient interfacial engineering strategy, offering insights for the design of high-performance semiconductor-based PEC photoelectrodes.

Read Full Abstract10.1016/S1872-5813(26)60647-0
Fe-modified MoS2/NC catalyst for hydrodeoxygenation of lignin into aviation fuel-range arenesGraphical AbstractVerified
Journal of Fuel Chemistry and Technology2026

Fe-modified MoS2/NC catalyst for hydrodeoxygenation of lignin into aviation fuel-range arenes

Lignin, as the sole renewable source of aromatic compounds, holds significant potential for producing green aviation fuel-range arenes via hydrodeoxygenation (HDO). In this study, a series of nitrogen-doped carbon-supported FeMoS/NC bimetallic catalysts were synthesized via a hydrothermal method. The HDO performance was evaluated using 4-ethylguaiacol as a model compound at 340 °C under 3 MPa H2. The unmodified MoS2/NC catalyst achieved a deoxygenation degree of 83.4%, whereas the Fe-modified catalyst with an optimal Fe/Mo molar ratio of 0.3 (Fe0.3MoS/NC) attained complete deoxygenation (100%) with an arenes selectivity of 78.6%. Beyond this optimal ratio, the deoxygenation degree inversely correlated with the Fe/Mo molar ratio. Characterization via XRD, TEM, BET, and XPS revealed that Fe incorporation enhanced the uniform dispersion of MoS2 on the NC support, increased surface acidity, and raised the concentration of sulfur vacancies, thereby promoting adsorption of oxygen-containing compounds. The HDO pathway over Fe0.3MoS/NC primarily proceeded via direct deoxygenation. When applied to real lignin under identical conditions (340 °C, 3 MPa H2, 12 h), the catalyst yielded 65.5% green hydrocarbons, with the C8–C16 fraction accounting for 54.4% of total hydrocarbons and an aromatic selectivity of 63.4% within this fraction. These results demonstrate that Fe0.3MoS/NC is a viable catalyst for selective conversion of lignin into green arenes suitable for sustainable aviation fuel applications.

Read Full Abstract10.1016/S1872-5813(26)60644-5
Chemical-Looping Methane Hydrogen Production Performance of Cu, La, Ce Modified Fe2O3/Al2O3 Oxygen CarriersGraphical AbstractVerified
Journal of Fuel Chemistry and Technology2026

Chemical-Looping Methane Hydrogen Production Performance of Cu, La, Ce Modified Fe2O3/Al2O3 Oxygen Carriers

Chemical looping methane steam reforming (CL-MSR) enables sequential production of high-selectivity syngas and high-purity hydrogen via redox cycling, yet single iron-based oxygen carriers suffer from poor cycling stability, low reactivity, and sintering. This study modified Fe2O3/Al2O3 oxygen carriers with Cu, La, and Ce additives via dip-coating, and systematically characterized their physicochemical properties, reactivity, and hydrogen production performance. Results showed that spinel-phase CuFe2O4 exhibited higher reactivity than perovskite LaFeO3 and CeO2, promoting deeper reduction of Fe2O3. Fe58Cu2Al achieved an oxygen storage capacity of 6.5 mmol/g. During CH4 reaction, Fe58Cu2Al exhibited the highest oxygen loss of 12.1 g/100 g oxygen carrier, with syngas yield of 5.15 mmol/g—1.33 and 1.59 times that of Fe60Al. In hydrogen production, the 2% Cu-modified carrier yielded 5.13 mmol/g H2, 1.51 times that of pristine Fe60Al, with purity exceeding 98%. After ten cycles, H2 yield remained at 3.61 mmol/g, surpassing the single-cycle output of pristine Fe60Al (3.39 mmol/g), demonstrating superior dispersion and coking resistance. The study establishes Cu modification as an effective strategy to enhance reactivity and cyclic stability of iron-based oxygen carriers for CL-MSR hydrogen production.

Read Full Abstract10.1016/S1872-5813(25)60630-X
Ring Formation Mechanism of C4H3 Radical and Acetylene in Soot Precursor FormationGraphical AbstractVerified
Journal of Fuel Chemistry and Technology2026

Ring Formation Mechanism of C4H3 Radical and Acetylene in Soot Precursor Formation

This study systematically investigates the cyclization reaction mechanisms between n-C4H3 (1-buten-3-yn-1-yl) and i-C4H3 (2-buten-3-yn-1-yl) radicals with acetylene (C2H2) using density functional theory (DFT) and transition state theory (TST). The results reveal that the reaction of n-C4H3 with acetylene proceeds via a radical chain mechanism through an addition-cyclization pathway, yielding phenyl (six-membered ring), fulvenyl (five-membered ring), and four-membered ring intermediates. The product formation rates follow the order: fulvenyl (five-membered ring) > phenyl (six-membered ring) > four-membered ring. For i-C4H3, the intermediate structures depend on the carbon position of i-C4H3 where acetylene addition occurs: addition at the C2 position predominantly generates fulvenyl (five-membered ring) as the primary product, whereas addition at the C4 position may lead to phenyl (six-membered ring), fulvenyl (five-membered ring), or four-membered ring intermediates, with the four-membered ring forming most rapidly and the six-membered ring the slowest. Theoretical analyses demonstrate that the selectivity of reaction pathways is primarily governed by structural differences between the isomers. This work provides atomic-scale insights into the cyclization processes between acetylene and C4H3 species, establishing a foundation for refining models of soot precursor formation.

Read Full Abstract10.1016/S1872-5813(25)60627-X
Efficient Leaching and Separation of Iron, Aluminum, and Calcium from Carbon-Rich Components in Coal Gasification Fine Slag Using Organic AcidsGraphical AbstractVerified
Journal of Fuel Chemistry and Technology2026

Efficient Leaching and Separation of Iron, Aluminum, and Calcium from Carbon-Rich Components in Coal Gasification Fine Slag Using Organic Acids

Coal gasification fine slag (CGFS) is a solid waste generated in large quantities during coal gasification, containing residual carbon and inorganic ash rich in SiO2, Al2O3, CaO, Fe2O3, and MgO. The carbon-rich components (CGFS-H) of CGFS, typically comprising 20–50% residual carbon, present both environmental challenges and opportunities for resource recovery. This study systematically investigates the selective leaching behavior of Fe3+, Al3+, and Ca2+ from CGFS-H using three organic acid extractants: citric acid, tartaric acid, and tetrasodium iminodisuccinate (IDS-4Na). The results demonstrate distinct selectivity: IDS-4Na exhibits the highest leaching yield and selectivity for Fe3+, achieving a single leaching yield of 41.2% while suppressing Ca2+ and Al3+ leaching to below 4%, with a selectivity ratio of Fe3+ to Al3+ and Ca2+ of 10.73. Tartaric acid effectively leaches both Fe3+ and Al3+, with single yields of 38.7% and 33.5%, respectively, while Ca2+ leaching remains below 5%, yielding a selectivity of Fe3+ and Al3+ relative to Ca2+ of 14.73. Citric acid preferentially leaches Ca2+, achieving a single yield of 71.5%, but also leaches Fe3+ and Al3+ at 35.2% and 39.1%, respectively, resulting in a low selectivity ratio of Ca2+ to Fe3+ and Al3+ of 0.96. Based on these selective affinities, a green stepwise separation method was developed using sequential leaching with IDS-4Na, tartaric acid, and citric acid. Under optimal conditions, cumulative leaching yields of 79.8% for Fe3+, 65.08% for Al3+, and 78.6% for Ca2+ were achieved. XRD, XRF, and SEM analyses elucidate the complexation mechanisms, indicating that the synergistic effects of selective coordination between structurally diverse organic acids and metal ions drive the process. This advancement provides a critical foundation for developing Ca/Fe/Al hydrotalcite materials using CGFS-H as a sustainable feedstock, promoting resource-efficient utilization of coal gasification fine slag.

Read Full Abstract10.1016/S1872-5813(25)60612-8
Design of Catalysts for Electrochemical Nitric Oxide Reduction to Ammonia Based on Stacked Ensemble LearningGraphical AbstractVerified
Journal of Fuel Chemistry and Technology2026

Design of Catalysts for Electrochemical Nitric Oxide Reduction to Ammonia Based on Stacked Ensemble Learning

The electrocatalytic reduction of nitric oxide to ammonia (NORR) is a key green energy conversion technology. Its efficiency relies on high-performance electrocatalysts to enhance both ammonia yield (YNH3) and Faradaic efficiency (FNH3). Conventional experimental screening methods are resource- and time-intensive. Here, machine learning combined with SHAP feature analysis was employed to establish a stacked ensemble model integrating multiple algorithms, enabling systematic investigation of key descriptors governing NORR performance based on an experimental dataset. Evaluation of eight model algorithms revealed that the Stacked-SVR model achieved an R² of 0.9223 and RMSE of 0.0608 for predicting YNH3 on the test set, while the Stacked-RF model achieved an R² of 0.9042 and RMSE of 0.0900 for predicting FNH3. The stacked ensemble model integrates strengths of individual algorithms, demonstrating strong prediction performance while avoiding overfitting. SHAP analysis revealed that Cu content in catalyst composition has the most significant impact on catalytic performance. Moreover, the combination of wet chemical reduction synthesis, carbon fiber (CF) conductive substrate, and HCl electrolyte is more favorable for enhancing catalytic activity. Additionally, moderately lowering working potential, controlling electrolyte volume at low-to-medium levels, reducing catalyst loading, and increasing electrolyte concentration synergistically enhance both YNH3 and FNH3.

Read Full Abstract10.1016/S1872-5813(25)60625-6
Influence of the Distance between Brønsted Acid Sites and Mo Sites in Mo/HZSM-5 on the Mechanism of Methane Dehydroaromatization PerformanceGraphical AbstractVerified
Journal of Fuel Chemistry and Technology2026

Influence of the Distance between Brønsted Acid Sites and Mo Sites in Mo/HZSM-5 on the Mechanism of Methane Dehydroaromatization Performance

Methane dehydroaromatization (MDA) offers a carbon-neutral route to benzene, toluene, and xylene (BTX), yet the regulatory mechanisms of Brønsted acid site (BAS) strength and spatial proximity to Mo sites remain unresolved. This study systematically tunes BAS strength via isomorphous substitution (Al, Ga, Fe, B) and Mo-BAS proximity in ZSM-5, integrating catalytic evaluations with density functional theory (DFT). Strongly acidic Al-zeolites achieve the highest methane conversion, while weakly acidic B-substituted systems exhibit optimal mono-/bifunctional synergy, outperforming moderate-acid counterparts. DFT reveals that deprotonation energy (DPE) correlates with acid strength; Al-ZSM-5 (DPE = -5.68 eV) lowers the C–H activation barrier (ΔG = 1.467 eV). Spatial proximity analysis shows that nanoscale Mo-BAS distances, achieved via ball milling, enhance methane conversion by 33% and BTX yield by 31% compared to micrometer-scale mixtures, by accelerating intermediate transport and suppressing coke. These findings establish a multi-scale framework linking acid strength, spatial confinement, and electronic modulation, providing actionable guidelines for designing next-generation MDA catalysts.

Read Full Abstract10.1016/S1872-5813(25)60631-1
The Role of Copper Valence States in CuZnAl Catalysts for CO2-to-Methanol ConversionGraphical AbstractVerified
Journal of Fuel Chemistry and Technology2026

The Role of Copper Valence States in CuZnAl Catalysts for CO2-to-Methanol Conversion

CuZnAl (CZA) is a classic industrial catalyst for methanol synthesis from syngas, but its catalytic performance for CO2 hydrogenation to methanol is suboptimal. The catalytic mechanism of Cu species in CZA remains challenging. This study systematically investigates the valence state changes of active Cu species in CZA catalysts and their influence on catalytic performance by modifying catalysts with varying amounts of electron donor K, thereby identifying the catalytic function of Cu species with different valence states. H2-TPR, XPS, and HR-TEM characterizations reveal that highly dispersed K species supported on CZA catalysts inhibit the reduction of CuO, resulting in a small amount of Cu2O active species being produced under reaction conditions, thus causing a decrease in catalytic activity. Furthermore, XRD and Cu LMM spectra show that the proportion of Cu0 in K-modified CZA catalysts increases with K loading, but a higher proportion of Cu0 species on the surface obviously promotes the reverse water gas shift (RWGS) reaction. According to the results of in situ infrared spectroscopy, CZA catalyst follows the reaction pathway mediated by HCOO* in the hydrogenation of CO2 to methanol.

Read Full Abstract10.1016/S1872-5813(25)60616-5
Oxidation Mechanism of Ethylene over MgO-Supported Ag-Cu Bimetallic Synergistic Catalysts: A DFT StudyGraphical AbstractVerified
Journal of Fuel Chemistry and Technology2026

Oxidation Mechanism of Ethylene over MgO-Supported Ag-Cu Bimetallic Synergistic Catalysts: A DFT Study

Ethylene (C2H4) in vehicle exhaust is a highly reactive volatile organic compound (VOC) whose photo-oxidation with NOx contributes to the formation of O3 and secondary organic aerosols (SOA), a key precursor of PM2.5. This study designs a novel MgO-supported Ag-Cu bimetallic catalyst and investigates its performance using density functional theory (DFT). The effects of Ag and Cu loading on geometric structure, stability, and reactant adsorption are analyzed, and the catalytic oxidation pathways of C2H4 over AgCu-MgO are elucidated. Results indicate that loading Ag significantly enhances C2H4 adsorption, with a maximum adsorption energy of -1.46 eV, while O2 adsorption remains weak (-0.45 eV). Cu-MgO shows moderate C2H4 adsorption (-0.87 eV at bridge site) but higher O2 adsorption (-0.76 eV). Among 17 AgCu-MgO dual-atom catalyst (DAC) configurations, those with Ag and Cu co-adsorbed at Mg sites are thermodynamically more stable (binding energies below -10 eV). Configurations with Ag and Cu in close proximity enhance co-adsorption of C2H4 and O2. C2H4 oxidation preferentially proceeds via C=C bond cleavage to form *CH3 and CO2. For three representative configurations (1, 3, 6), free energy barriers for rate-limiting steps in the *HCO and CH2O pathway are consistently higher than those for *CH3 and CO2 pathway. Configuration 6 exhibits the lowest energy barrier (0.32 eV) for its rate-limiting step, indicating the highest catalytic performance. This study provides atomic-scale insights for rational design of efficient catalysts targeting olefinic pollutants in automotive emissions.

Read Full Abstract10.1016/S1872-5813(26)60640-8