SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-026-4202-3
Carbon dots (CDs) with absorption in the second near-infrared window (NIR-II, 900-1700 nm) hold promise for tumor theranostics, yet existing synthesis methods often involve complex procedures, harsh conditions, or lack precise control. Here we report a 'self-photooxidation-restructuring' strategy that enables structural reorganization of the carbon core in CDs, achieving a significant redshift of absorption into the NIR-II region. Under ultraviolet (UV) light irradiation, the precursor (B-CDs, absorption in UV region) generates singlet oxygen, which self-oxidizes aldehyde groups and the carbon skeleton of B-CDs to stronger electron-withdrawing carboxyl groups and carbon radicals, respectively. These processes facilitate the formation of new C=C bonds between isolated aromatic domains, thereby transforming B-CDs into novel CDs (N-CDs) characterized by enhanced donor-acceptor interactions and a redshift in absorption toward the NIR-II window. Various experimental data, including high-resolution XPS, FTIR, NMR, EPR, have proved the proposed formation mechanism. The novel N-CDs afforded a high photothermal conversion efficiency of up to 71.33%, which enabled 1064 nm laser-activated photoacoustic imaging (PAI)-guided photothermal therapy (PTT) in tumors. This work opens a new avenue for the synthesis and modulation of CDs in the NIR-II region.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3664-x
The proliferation of electronic devices and wireless communications has escalated the demand for materials that simultaneously provide electromagnetic interference (EMI) shielding and infrared (IR) thermal camouflage, a combination critical for military and civilian applications. Traditional metallic shields suffer from high density, poor processability, and cost, while polymer-based alternatives often lack sufficient shielding effectiveness and environmental stability. Here, we report a multilayer composite film fabricated via layer-by-layer vacuum filtration and hot-pressing, integrating modified aramid nanofibers (ANF) and MXene (Ti3C2Tx) nanosheets. The film architecture comprises ANF-polypyrrole (ANF-PPy) as the matrix and Ag-MXene as the functional filler, with in-situ grown Ag nanoparticles intercalating between MXene layers to enhance interlayer spacing and electromagnetic wave scattering. At a thickness of only 33 μm, the film achieves an average EMI shielding effectiveness (SE) of 66.75 dB and a specific shielding effectiveness (SSE/t) of 38432.54 dB cm2 g−1. The multilayer structure promotes multiple internal reflections and interfacial polarization losses, while the tight integration ensures high IR reflectivity. This work establishes a foundation for developing multifunctional protective materials with dual EMI shielding and IR camouflage capabilities, addressing the critical bottleneck of simultaneous performance in ultrathin, flexible formats.
Environmental Chemistry•2026•DOI: 10.7524/j.issn.0254-6108.2025092802
Activated carbon (AC) filters in drinking water treatment plants (DWTPs) experience significant adsorption performance decline over extended operation, yet complete media replacement is a major cost. To evaluate cost-effective strategies, pilot-scale column experiments with five AC replacement ratios (0%, 30%, 50%, 70%, and 100%) were conducted to assess removal of disinfection by-product (DBP) precursors and pesticide-related emerging contaminants. For dissolved organic matter (DOM), all fractions except low molecular weight compounds (LMWC) achieved >85% of the removal obtained with full replacement when 70% new AC was used, with UV254 removal reaching 70%. LMWC, due to small molecular size and low adsorption energy, required higher replacement ratios or full replacement for substantial removal. For DBPs, removal of trihalomethanes (THMs) and haloacetic acids (HAAs) was insensitive to replacement ratio, while haloacetaldehydes (HALs) removal improved markedly with increasing ratio, indicating structural selectivity. For pesticide-related contaminants, all except triazoles achieved >95% removal at 70% replacement; triazoles, due to high water solubility, high polarity, and low octanol-water partition coefficient, achieved only ~60% removal. Overall, replacing 70% of AC restored treatment performance to >80% of that with full replacement, ensuring effluent quality while saving ~30% of new carbon cost. Molecular structure, polarity, and pore size matching are key determinants of removal efficiency; optimizing replacement ratio balances water quality and economic benefits.
Journal of Environmental Engineering Technology•2026•DOI: 10.13205/j.hjgc.202605017
In response to the escalating challenge of industrial dust pollution, this study introduces a magnetic field-enhanced electrostatic dust collector integrated with wire mesh filtration. By applying an external magnetic field, the conventional electrostatic precipitation process is physically intensified. Systematic experiments compared discharge characteristics and dust removal efficiency with and without magnetic field intervention. The influence of wire mesh structural parameters was investigated, focusing on pore size (1, 2, 3 mm), number of stacked layers (1, 2, 3), and surface composite filtration materials (polyethylene filter mesh, polyamide mesh). Additionally, the effects of airflow velocity (1–5 m/s), inlet flow direction (forward/reverse), and dust type (fly ash, coal combustion dust, cement ash) on removal efficiency were tested. Results demonstrate that the optimized magnetic field-wire mesh coupling significantly enhances the charging and capture of fine dust. Specifically, smaller mesh apertures improve efficiency, with 1 mm yielding the best performance. Increasing the number of mesh layers effectively enhances efficiency at discharge voltages of 13–17 kV. Coating the mesh with either polyethylene or polyamide further improves efficiency, with negligible difference between the two materials. Reverse airflow direction results in lower effective gas velocity due to opposing gravity and drag forces, yet the combined magnetic and electric fields stabilize particle charging and enhance trajectory deflection, leading to improved overall performance. Dust resistivity is a critical factor: lower resistivity facilitates charging, while higher resistivity induces back corona, reducing efficiency. Magnetic field enhancement mitigates back corona and improves removal, particularly for high-resistivity cement ash. These findings offer a viable technical solution for efficient industrial flue gas dedusting.
Chinese Journal of Environmental Engineering•2026•DOI: 10.12030/j.cjee.202510041
This study presents a full-scale engineering practice of retrofitting an idle upflow anaerobic sludge blanket (UASB) reactor into an aerobic granular sludge (AGS) system for treating low-strength municipal wastewater. The design capacity was 20,000 m3/d (maximum 24,000 m3/d), achieving separate treatment of industrial and domestic wastewater to reduce operational costs. Systematic analysis covered hydraulic capacity enhancement, effluent quality, pollutant removal efficiencies, sludge granulation progress, and operational costs. Results showed rapid start-up: the system reached 75% of design capacity by day 10 and 90% by day 26. During a 4-month operation, average removal efficiencies for COD, NH4+-N, TN, and SS were 83.2%, 97.0%, 75.9%, and 94.4%, respectively, even under low influent BOD5/TN ratios (typically below 4). Granulation progressed quickly: by day 44, average particle size was 2.6 times that of the inoculum and over 4 times that of flocs, with granules (>200 μm) accounting for 17.3%; by day 110, these values increased to 3.2 times and 5 times, with granule proportion reaching 33.4%. Compared to the previous year (June–August), the AGS process reduced electricity consumption, chemical consumption, and sludge production by 77.3%, 25.4%, and 30.4%, respectively, while saving 65.6% of footprint. This ten-thousand-ton case provides a practical basis for AGS technology application in China.
Environmental Chemistry•2026•DOI: 10.7524/j.issn.0254-6108.2025032004
This study proposes an integrated source apportionment framework that synergistically integrates pollution source classification, atmospheric dispersion modeling, backward trajectory analysis, weighted trajectory clustering, and forward contribution estimation to accurately target peak reduction at localized air pollution hotspots. Applied at the County-Town Scale in Beijing, this method was employed to investigate pollution episodes at the Tongzhou Dongguan monitoring site. Source classification relied on a pollution fingerprint database and temporal concentration profiles, while local contributions were quantified through combined air quality modeling and monitoring data. Forward and backward trajectory analyses enabled the identification of potential source regions and key contributors. Results indicate that construction dust, road dust, and emissions from the catering industry were the dominant local sources, with construction and road dust contributing most prominently to PM2.5 concentrations. Furthermore, abnormal PM2.5 increases were closely linked to low boundary layer height, weak winds, and high humidity, emphasizing the role of meteorological conditions in pollution accumulation. The proposed framework proves effective in pinpointing local pollution sources and offers a scientific basis for targeted air quality management at finer spatial scales.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3910-0
Perovskite photovoltaics (PVs) have emerged as leading candidates for next-generation solar technology due to low production costs, high efficiencies, and compatibility with large-area manufacturing. However, commercialization faces bottlenecks: toxic solvents, non-uniform film quality over large areas, and insufficient operational reliability. Wang et al. developed a green-solvent ink and a solvent-confinement edge-protection (SCEP) strategy to address these issues. By increasing the fraction of 2-methyltetrahydrofuran (2-MeTHF) in a gamma-valerolactone (GVL) based solvent system, they weakened perovskite-GVL coordination, accelerated solvent extraction during vacuum-chamber drying, and promoted rapid supersaturation toward the desired alpha-phase while suppressing the non-perovskite delta-phase. This resulted in perovskite films with enlarged grains, reduced voids, and improved crystallinity in ambient air. To mitigate edge effects during slot-die coating, they incorporated a cationic surfactant, trimethyltetradecylammonium chloride (TAC), which self-assembled at the liquid-vapor interface, reducing surface tension and inducing Marangoni flow to equalize evaporation. This SCEP strategy suppressed rapid edge evaporation, leading to uniform film morphology. The best-performing modules achieved a total area of 7200 cm², with J-V curves and stabilized efficiency certifications from NREL and TÜV Rheinland, demonstrating commercial viability. This work provides a unified framework for solvent design and process control, advancing perovskite PV modules toward industrial production.
Chinese Journal of Environmental Engineering•2026•DOI: 10.12030/j.cjee.202510044
The efficient treatment of sulfur-containing volatile organic compounds (S-VOCs) has become a critical task for air pollution control and green low-carbon transition under China's 14th Five-Year Plan. Industrial emissions often contain multiple S-VOC species, whose interactions can complicate degradation pathways, generate uncontrollable byproducts, and deactivate catalysts, limiting practical application. This review systematically summarizes the past decade of research on catalytic degradation of thiols and thioethers in multi-pollutant systems, focusing on competitive adsorption mechanisms, interfacial reaction pathways, and environmental factor regulation. Performance differences and reaction mechanisms across various catalyst systems under coexisting S-VOCs and inorganic sulfur are compared. Key findings indicate that mixed thiol systems exhibit faster deactivation than single-component systems due to temperature-dependent competitive adsorption and pathway switching, governed by molecular size–active site matching. Strategies such as metal–support strong interactions, zeolite confinement, nanocluster effects, and single-atom catalysts have improved activity and stability. However, dynamic competition mechanisms at active sites remain unresolved. Future research should develop atomic/molecular-level characterization techniques and multi-variable kinetic models, and shift from end-of-pipe purification to resource recovery, e.g., converting H2S and thiols into high-value chemicals like methanethiol, achieving dual goals of pollution control and sulfur resource recycling.
Journal of Environmental Engineering Technology•2026•DOI: 10.13205/j.hjgc.202608015
Inter-basin water diversion projects can profoundly alter the water quality dynamics of receiving basins. Taking the Qincun Reservoir and its downstream reaches in the Huangze River Basin as a case study, this research quantitatively evaluates water-quality responses under multiple coordinated management measures. An integrated Environmental Fluid Dynamics Code-Soil and Water Assessment Tool (EFDC-SWAT) modeling framework was established, coupling a two-dimensional hydrodynamic-water-quality model for the reservoir with a hydrology-water-quality model for the downstream reaches. Seven management scenarios were designed to reflect various combinations of point- and non-point-source pollution control strategies. Simulations focused on spatiotemporal variations in key indicators—total nitrogen (TN), total phosphorus (TP), ammonia nitrogen (NH3-N), and permanganate index (CODMn)—and assessed pollution-load reduction effectiveness. Comparative analysis using the comprehensive water quality identification index (CWQII) revealed that under Scenario 3 (highest pollution-control standards with lowest diversion volume), TN and TP concentrations in the reservoir decreased by 80% and 50%, respectively, achieving Class II water-quality standards. Downstream TN and TP levels declined by 36% and 33%, and the CWQII improved from 4.211 to 3.410. Land consolidation contributed 77% and 45% to TN and TP load reductions in the reservoir, respectively, while a 20% reduction in diversion volume was most effective in improving downstream TN (>50%). These results demonstrate that the coupled EFDC-SWAT model effectively elucidates mechanisms through which inter-basin water diversion influences water quality in supply areas. Moreover, synergistic point- and non-point-source controls exhibit a nonlinear enhancement effect on overall water-quality improvement.