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Journal of Environmental Chemical Engineering · 2026 ·Vol. 14 ·期 5 ·124477 · IF 7.5

Morphology-dependent surface phosphorylated Co3O4 for enhanced chlorobenzene oxidation and chlorine resistance

Ke Yin,Juntai Tian,Ziwei Wang,Bichun Huang

Morphology engineering is an effective strategy to regulate the catalytic performance of transition metal oxides for chlorinated volatile organic compound (CVOCs) elimination, yet the morphology-dependent response to surface modification and its intrinsic mechanism remain insufficiently understood. Herein, cubic Co 3 O 4 -c and plate-like Co 3 O 4 -p with distinct surface defect densities were selected as model catalysts to systematically reveal the morphology-dependent effect on chlorobenzene (CB) oxidation, with surface phosphorylation employed as a regulated means to probe the intrinsic morphology-dependent regulation mechanism. Surface phosphorylation exhibits a significant morphology-dependent feature. It retains the intrinsic spinel structure of Co 3 O 4 and triggers surface electronic redistribution via constructed Co–O–P bonds. High-defect Co 3 O 4 -p presents favorable responsiveness to phosphorylation, which synchronously boosts acid sites, surface Co 3 + proportion and adsorbed active oxygen content. By contrast, phosphate species partially cover surface active sites of low-defect Co 3 O 4 -c, leading to activity decline. The optimized HP-Co 3 O 4 -p delivers a T 90 value of 330 ℃ toward CB combustion, 23 ℃ lower than pristine Co 3 O 4 -p, and retains 84% conversion after 10 h reaction with mitigated attenuation. Mechanism analysis demonstrates that the morphology-dependent effect originates from the difference in surface defect density. On high-defect Co 3 O 4 -p, P–OH groups supply protons to facilitate C–Cl bond activation and HCl desorption, and phosphate moieties alleviate chlorine enrichment and restrain polychlorinated byproducts. This work reveals the morphology-dependent phosphorylation mechanism of Co 3 O 4 and guides the rational design of efficient CVOCs catalysts.

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Environments · 2026 ·Vol. 13 ·期 8 ·426 · IF 4.3

Adsorption–Catalysis Dual-Function Nitrogen-Doped Carbon/CoFe2O4 Composite for Efficient Tetracycline Removal

Xuekai Wang,Xiangwu Meng,Mengtian Zhang,Kai Li,Lichun Mao,Lu Zhong,Jianjun Li

Efficient removal of tetracycline (TC) from antibiotic-contaminated wastewater remains a significant challenge. In this study, a nitrogen-doped carbon modified cobalt ferrite (C@CoFe2O4, CF) composite was synthesized via a one-step hydrothermal method, and its adsorption–catalysis dual-function performance was systematically evaluated. Structural characterization revealed that CoFe2O4nanoparticles were locally encapsulated by an N-doped carbonaceous layer, providing a high specific surface area and abundant nitrogen-containing active sites. Under optimized conditions, the CF-3/PMS system achieved 93.44% TC removal within 45 min, while CF-3 exhibited a maximum adsorption capacity of 486.5 mg·g−1. Radical quenching experiments suggested that singlet oxygen (1O2) and superoxide radicals (O2•−) played major roles in TC oxidation, while sulfate radicals (SO4•−) and hydroxyl radicals (HO•) also contributed, indicating the coexistence of radical and non-radical oxidation pathways. TC adsorption was driven by surface complexation, π–π electron donor–acceptor interactions, and hydrogen bonding. The enhanced TC removal performance may arise from the cooperative contributions of N-containing carbon sites, accessible Co/Fe-containing regions, and interfacial electronic interactions, which promote TC enrichment and PMS-mediated oxidation. This work provides a promising strategy for designing bifunctional materials for antibiotic wastewater treatment.

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Advanced Science · 2026 · IF 14.1

Multi-Stimuli Responsive Magneto-Coacervate Droplets for Selective Molecular Enrichment and Programmable Manipulation

Kailang Liu,Haocheng Ran,Haohui Ou,Peiying Chen,Cheng Qi,Tiantian Kong,Zhou Liu

Coacervate droplets formed via liquid–liquid phase separation offer unique opportunities as microreactors and delivery vehicles due to their ability to selectively concentrate biomolecules and support biochemical reactions. However, their passive nature severely restricts precise spatial and temporal control, posing barriers to practical implementation. Here, we report magneto-coacervate droplets constructed from gelatin, poly(diallyldimethylammonium chloride) (PDDA), and superparamagnetic Fe 3 O 4 @SiO 2 nanoparticles. These magneto-coacervate droplets exhibit reversible sol–gel transitions controlled by temperature and pH, tunable surface charge properties for electrostatically driven molecular enrichment, and precise three-dimensional manipulation under external magnetic fields. These magneto-coacervate droplets can serve as multifunctional platforms, greatly increasing the practical use of phase-separated microreactors in environmental remediation, biochemical processing, and targeted biomedical interventions. Demonstrated applications include efficient capture and recycling of microplastic pollutants, magnetically enhanced catalytic enzyme cascades with reaction rates 2–3 times higher than those of conventional methods, and targeted vascular embolization through controlled in situ gelation.

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ADVANCED FUNCTIONAL MATERIALS · 2026 ·Vol. 36 ·期 63 ·e77025 · IF 19.9

MXene–Ag2Se@sponge Dual-Modal Sensor for Decoupled Temperature and Pressure Sensing

Xuan Weng,Peilin Li,Chenyang Jia,Xinkai Guo,Wen Sun,Hai Jiang

Flexible sensors are evolving from single-parameter to multi-modal measurement. Dual-modal flexible tactile sensors capable of detecting both temperature and pressure are essential for human–machine interaction and wearable health monitoring. Here, we present a flexible dual-modal sensor constructed from a sponge framework decorated with MXene–Ag 2 Se nanocomposite. The heterogeneous MXene–Ag 2 Se interfaces enhance carrier transport and conductivity. A three-electrode configuration with spatially separated in-plane thermoelectricity and out-of-plane piezoresistivity enables effective decoupling of temperature and pressure sensing. The MXene–Ag 2 Se@sponge sensor demonstrates high pressure sensitivity (2.202 kPa − 1 in 0–25 kPa, 0.466 kPa − 1 in 25–60 kPa, and 0.076 kPa − 1 in 60–300 kPa), a fast response time (37 ms) for pressure sensing, and excellent durability. For temperature sensing, it achieves an ultralow detection limit of 0.2 K, a high Seebeck coefficient of 175.47 µV/K, and stable cycling performance. In addition, the MXene–Ag 2 Se@sponge dual-modal sensor is applied to human pulse monitoring, joint motion detection, and finger temperature measurement, highlighting its potential for wearable biomedical sensing. Furthermore, a sensor array was also implemented as electronic skin, enabling simultaneous temperature-pressure mapping with high spatial resolution. This work provides a promising strategy for intelligent robotics and flexible electronics.

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Food Bioscience · 2026 · IF 6.2

Polydopamine-modified 3D ordered micropillar arrays for uniform and dense immobilization of silver nanoflowers toward ultrasensitive SERS detection of multiple pollutants

Jiwei Song,Yunpeng Shao,Yuan Yao,Zicheng Zhang,Yaqin Ren,Linyu Mei

Surface-enhanced Raman scattering (SERS) has emerged as a powerful analytical technique for ultrasensitive and rapid detection. However, the performance of SERS substrates largely depends on their ability to generate intense localized electromagnetic fields at nanoscale hot spots, while simultaneously achieving high sensitivity and signal reproducibility remains a major challenge. In this work, a highly ordered SU-8 micropillar array was fabricated by Ultraviolet Lithography(UL), followed by biomimetic modification with polydopamine (PDA) to achieve the uniform immobilization of silver nanoflowers (AgNFs). The resulting three-dimensional (3D) AgNFs/PDA/SU-8 micropillar SERS substrate integrates the structural advantages of the 3D architecture, the abundant electromagnetic hot spots and physical enrichment effect generated by densely packed AgNFs, and the interfacial regulation provided by PDA, thereby synergistically enhancing the SERS performance. The substrate exhibited an enhancement factor(EF) of 2.16 × 10 9 for Rhodamine 6G (R6G), with an experimental limit of detection as low as 1 × 10 −14 M (S/N = 3) and a relative standard deviation below 8.30%. Furthermore, the limits of detection for enrofloxacin (ENR), clothianidin (CLO), and 100 and 800 nm polystyrene (PS) particles in seawater reached 1 × 10 −13  M, 1 × 10 −14  M, 2.5 μg mL −1 , and 0.6 mg mL −1 , respectively. Simultaneous detection of multiple contaminants was also successfully achieved in complex food matrices, including mineral water, milk, and liquor. This work provides an effective strategy for constructing high-performance 3D SERS substrates and demonstrates their promising potential for food safety monitoring and aquatic environmental analysis.

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ENVIRONMENTAL POLLUTION · 2026 · IF 7.2

Unveiling N-nitrosomorpholine precursors in wastewater using nontarget, target analysis and transformation mechanism

Jing Zhou,Bo Zhao,Jie Liu,Junhan Ruan,Li Lin,Yi Li

N -nitrosomorpholine (NMOR), as a highly carcinogenic N -nitrosamine, has been widely detected in urban sewer systems. NMOR ranged from 27.2 to 817 ng/L in winter, follow by summer (2.09–453 ng/L), in raw wastewater collected from pumping stations connected to a Wastewater Treatment Plant (WWTP). Especially in winter, NMOR was detected (200–295 ng/L) in the influent, with residue of 98.0–116 ng/L in the effluent. Therefore, it is necessary to control NMOR before the WWTP. However, the corresponding precursors and transformation mechanisms in sewer systems are not yet fully understood. This study has identified NMOR precursors in sewer systems by nontarget analysis combined with targeted analysis. NMOR formation was confirmed by nitrosation and chloramination through distinct pathways from a known (morpholine, MOR) and two unreported ( N -methylmorpholine, NMM and N -methylmorpholine- N -oxide, NMMO) precursors. In addition, NMM and MOR were detected up to 8.65 and 14.3 μg/L in raw wastewater, as well as up to 0.250 and 1.17 μg/L in the effluent. NMOR formation by chloramine could reach to 73.0 ng/L. This study demonstrated the extensive presence of NMOR precursors in raw and treated wastewater, in which new identified precursor NMM might significantly contribute formation of NMOR.

CAS / MDL: 1336-21-6
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2026 · IF 9.6

Gas marble-film reactors with programmable particle shells and capillary–granular stability

Qin Yao,Meiling Liang,Kunling Yang,Cheng Qi,Tiantian Kong,Bernard P. Binks,Zhou Liu

Motivated by gas-accessible thin liquid films in lung alveoli, we develop gas marble-film reactors in which particle-stabilized bubbles confine an ultrathin freestanding liquid film within a jammed solid shell. Hexagonal PET (poly(ethylene terephthalate)) plates, in addition to conventional spherical particles, generate faceted gas marbles with planar film regions that improve optical access. We quantify the pressure limits of microsphere- and plate-stabilized shells during inflation and deflation, and describe their response using a capillary–granular framework. In this framework, inflation rupture is governed by capillary breakthrough at particle-defined throats, whereas deflation collapse reflects the combined resistance of capillarity and interparticle jamming. The mechanically defined films then serve as gas-accessible interfacial reactors in two proof-of-concept demonstrations. In a Tollens reaction, aerosolized glucose delivery through the external gas phase localizes silver reduction to liquid-wetted regions of the particle shell, producing spatially patterned silver-deposited microspheres. In biological assays, plate-stabilized shells provide flat observation windows for monitoring aerobic E. coli growth and its inhibition by levofloxacin. These results establish gas marbles as programmable colloidal film reactors whose structure, pressure stability, and interfacial function can be coupled through particle geometry and capillary jamming. Download: Download high-res image (101KB) Download: Download full-size image

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CERAMICS INTERNATIONAL · 2026 · IF 6

Gelcasting of ZTA/Cr2O3 ceramics for pressureless sintering of complex components: slurry rheological properties and mechanical properties

Zhengjia Zhu,Hui Chen,Yushuai Bai,Jingjie Zhang,Mingdong Yi,Zhaoqiang Chen,Guangchun Xiao,Chonghai Xu

ZTA/Cr 2 O 3 ceramics were fabricated by gelcasting via gelcasting followed by pressureless sintering. The effects of pH, dispersant content, ball-milling time, solid loading, and Cr 2 O 3 content on slurry rheological properties, green body properties, sintering densification behavior, and mechanical properties were investigated. The addition of Cr 2 O 3 effectively decreased slurry viscosity and improves flowability, facilitating the preparation of high-solid-loading slurries. The green body relative density and flexural strength reached optimum values at a solid loading of 54 vol%, reaching 54.83% and 19.7 ± 0.27 MPa, respectively. After sintering at 1600 °C for 3 h, the optimum mechanical properties were obtained at a Cr 2 O 3 content of 0.4 vol%. The Vickers hardness, flexural strength, and fracture toughness were 17.17 ± 0.26 GPa, 581.22 ± 9.20 MPa, and 6.59 ± 0.32 MPa m 1/2 , respectively. Compared with Cr 2 O 3 -free ZTA ceramics, the hardness, flexural strength, and fracture toughness increased by 5.5%, 17.58%, and 10.75%, respectively. The enhanced mechanical properties are mainly attributed to the synergistic effects of the solid-solution incorporation of Cr 3+ in the α-Al 2 O 3 lattice, the resulting changes in lattice parameters, grain refinement, improved densification, and enhanced stability of the t-ZrO 2 phase. Furthermore, complex-shaped ZTA/Cr 2 O 3 ceramic components were successfully fabricated, showing no visible defects and uniform shrinkage after sintering, providing useful guidance for the near-net-shape fabrication of high-performance ceramic components.

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ACS Applied Polymer Materials · 2026 ·Vol. 8 ·期 14 ·11084-11103 · IF 5.2

Decoupling Adhesion and Photon-Regulated Curing via Superamphiphobic and Quantum Dot-PDMS Dual Functional Coatings in Vat Photopolymerization

Muniyandi Vigneshwaran,Mansoor Farukh,Chen Weiqiang,Li Yan,Weng Zixiang,Thirunavukkarasu Naveen,Wu Lixin

Unstable layer detachment and uncontrolled interfacial curing remain critical limitations in conventional bottom-up photopolymerization resin vats, where high-surface-energy release films promote strong resin-vat adhesion, and unrestricted photon flux at the resin-vat boundary leads to excessive bottom-layer cross-linking, together resulting in mechanical disturbance during separation and dimensional inaccuracy. To address these coupled challenges, this study reports a dual-interface engineered resin vat that decouples interfacial adhesion and curing regulation through independent material design. A superamphiphobic superlow-adhesion interface (SLAI) minimizes interfacial bonding at the release surface, while a carbon quantum dot-incorporated polydimethylsiloxane (CQD-PDMS) optical layer is introduced at the vat window to modulate interfacial photon flux and confine polymerization within the intended layer thickness. Compared with the conventional release film interface, the proposed synergistic interfacial control significantly reduced separation forces during layer detachment from 5 to 15 N to 0.25–3 N, depending on resin viscosity and processing conditions, corresponding to a maximum reduction of up to 95% under optimized conditions. Simultaneously, dimensional fidelity was substantially improved, reducing the Z -direction deviation from approximately 7% to 0.2%. Importantly, the optical modification preserves high transparency and demonstrates stable performance over 10,000 consecutive printing cycles. By establishing a materials-driven strategy that simultaneously regulates adhesion energy and interfacial curing density, this work provides a scalable pathway for stabilizing detachment mechanics and enhancing dimensional precision in vat photopolymerization without altering the resin chemistry.

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ACS Applied Nano Materials · 2026 ·Vol. 9 ·期 29 ·13721-13740 · IF 5.8

Dual-Functional Janus Nanoparticles for Synergistic Antibacterial-Antitumor Therapy in Oral Squamous Cell Carcinoma

Yuan Yifang,Wang Chaoli,Li Na,Chen Hongwei,Zhou Zichao,Zhang Chongyang,Zhang Haiou,Wang Shengchao,Yu Qing,Cheng Xiaogang,Jiang Wenkai

Intratumor microorganisms can promote tumor initiation, development, metastasis, and therapeutic resistance in cancer. Previous studies have indicated that Porphyromonas gingivalis ( P. gingivalis ) accelerates the progression of oral squamous cell carcinoma (OSCC) through enhancing cancer cell stemness, promoting immune evasion, regulating cyclins, modulating inflammatory cytokine profiles, and remodeling the tumor microenvironment. In this study, a high detection rate of intratumor and intracellular P. gingivalis was observed in OSCC clinical patients, which suggested a potential association between P. gingivalis and OSCC pathogenesis. However, whether synergistic elimination of P. gingivalis during antitumor therapy can slow OSCC progression remains unknown. Thus, we engineered an anisotropic Janus nanoparticle-based drug delivery system utilizing Au nanoparticles (AuNPs) and porous silica carriers for tumor-targeted synergistic therapy. The Au–Ce6–SiO 2 -MTZ Janus nanoparticles (denoted as JCM) prevent primary tumor growth through the photosensitizer Chlorin e6 (Ce6)-mediated photodynamic therapy (PDT) and eliminate intracellular P. gingivalis via metronidazole (MTZ) simultaneously. Our results demonstrate that the Au–Ce6–SiO 2 -MTZ Janus NPs enhance targeted nanomedicine delivery to tumor sites and improve the relevant therapeutic outcomes of P. gingivalis -infected models by synergistic antitumor-antibacterial in vitro and in vivo . Overall, this study introduces an effective OSCC treatment using a Janus nanoplatform that integrates antibacterial and photodynamic functions. It successfully targets tumor-promoting P. gingivalis , enhancing antitumor efficacy compared to PDT alone, while ensuring good biocompatibility.

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Water · 2026 ·Vol. 18 ·期 14 ·1694 · IF 3.5

Occurrence, Spatiotemporal Distribution, Source Apportionment, and Ecological Risk Assessment of PPCPs in the Taipu River, a Strategic Trans-Boundary Water Source in Eastern China

Deling Fan,Yucen Liu,Wen Gu,Shuai Sun,Weilong Xing,Zhen Wang,Lili Shi,Lei Wang,Zheng Fang

Pharmaceuticals and personal care products (PPCPs) are contaminants of emerging global concern, yet their long-term fate and distribution in strategic trans-boundary water source areas remain underexplored. This study conducted a comprehensive monitoring campaign spanning from 2018 to 2020, with six sampling campaigns carried out in August 2018, December 2018, May 2019, August 2019, December 2019, and May 2020, to investigate the occurrence, spatiotemporal dynamics, source apportionment, and ecological risks of 54 PPCPs in the surface water and sediments of the Taipu River in eastern China. Utilizing non-target screening via liquid chromatography high-resolution mass spectrometry (LC-HRMS), 54 PPCPs across 15 categories were detected, with average total concentrations of 28.60 ng/L in surface water and 13.01 ng/g in sediments. Sulfonamides, quinolones, and non-steroidal anti-inflammatory drugs (NSAIDs) dominated the aqueous phase (with bisphenol A and sulfamethoxazole highly prevalent), while hormones (e.g., estriol) and quinolones (e.g., ciprofloxacin (CIP)) exhibited significant accumulation in the benthic zone. Spatiotemporal analysis revealed a seasonal pattern where PPCP concentrations were higher in the dry season than in the wet season, primarily driven by hydrological dilution and climate-induced degradation. Furthermore, Positive Matrix Factorization (EPA PMF 5.0) extracted five distinct source factors for each matrix. Specifically, surface water pollution was primarily driven by domestic wastewater, municipal effluents, medical discharges, and localized pharmaceutical emissions, whereas sediments acted as a long-term sink predominantly for domestic wastewater, agricultural/veterinary runoff, and municipal/industrial emissions. Ecological risk assessment indicated that while most of the nine high-frequency contaminants posed low risks, specific compounds such as CIP, SM2, and E3 presented medium risks in surface water, whereas ENR, CIP, and SPI posed medium risks in sediments. These findings emphasize that the continuous multi-source input and the resulting pseudo-persistence of PPCPs in sediments warrant prioritized continuous attention and targeted pollution control strategies in the Taipu River Basin.

CAS / MDL: 1336-21-6 64-18-6
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2026 · IF 8.7

Identification of a commercial Xylan as a microfold cell-targeting polysaccharide in vivo and in vitro

Jing Li,Mingxiao Feng,Niping Chen,Pengfei Shan,Hauyee Fung,Xueting Zhang,Singwan Pun,Yulin Sun,Chuying Huo,Wenting Zhao,Peili Zhu,Simin Qi,Shanlong Tang,Junmei Xia,Lifeng Li,Quanbin Han

Commercial Xylan undergoes efficient Microfold cell-mediated transport in vitro and in vivo . • Xylan possesses a β -(1 → 4)-linked backbone, branched with α -(1 → 2)-linked 4- O -methyl-glucuronic acid residues. • Uromodulin is predicted and validated as a potential receptor mediating Xylan transport. Microfold cells (M cells) in the gut serve as a key gateway to enhance the potency of oral vaccines. Although natural polysaccharides show promise as carriers, their development is limited by inherent drawbacks such as scarce availability and lack of intrinsic targeting capacity. Therefore, it is essential to identify suitable materials from well-defined, commercially available polysaccharide standards. In this study, a library of well-defined, high-purity commercial polysaccharides was screened, and identified Xylan as a lead candidate with superior M cell transport efficiency in an in vitro human M-like cell model. This transport was confirmed in vivo , where mass spectrometry quantified a significant delivery (2.45–9.97 μg) of Xylan into murine Peyer's patches. Structural confirmation via monosaccharide composition, enzymatic oligosaccharide profiling, methylation, and NMR analyses identified this active polymer as a β -1, 4-Xylan branched with α -1, 2-glucuronic acid bearing methyl substitution. Mechanistically, molecular docking predicted the M cell surface protein Uromodulin (Umod) as a potential receptor, a hypothesis subsequently validated by isothermal titration calorimetry and surface plasmon resonance. In conclusion, our findings reveal that a specific, commercial Xylan is selectively transported by M cells, a process potentially mediated by Umod, highlighting its great promise as a novel and well-defined carrier for oral vaccine development. Download: Download high-res image (263KB) Download: Download full-size image

CAS / MDL: 1336-21-6 631-61-8
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