JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
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2025
·
IF 6.2
Chunqi Yu,Yingqi Wang,Ke Wang,Shuai Zhang,Xiaopeng Hu,Yiwei Liu,Jiajia Xi
Chlorpyrifos (CPF) poses severe environmental and health risks, driving the need for on-site monitoring tools. This study presents a novel dual-recognition colorimetric sensor for ultrasensitive detection of CPF by coimmobilizing molecularly imprinted polymers (MIPs) and aptamers onto bimetallic Fe,Zr-MOF composites. The resulting Fe,Zr-MOF/Apt/MIP hybrid synergistically merges the structural robustness of MIPs with the conformational specificity of aptamers, while also functioning as both a nanocarrier and a peroxidase mimic. Notably, CPF binding sterically hinders substrate diffusion to catalytic sites, enabling quantitative detection via dose-dependent inhibition of TMB oxidation. The optimized sensor exhibits exceptional performance: a broad linear range (1–120 ng mL–1), ultralow detection limit (0.105 ng mL–1), and high specificity against interferents. When validated with complex matrices (apples, pears, and cabbage), it achieved satisfactory recoveries (91.0–110.0%). This work establishes a field-deployable strategy for on-site pesticide monitoring in food and environmental safety.
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高影响因子
JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY
·
2020
·Vol. 20
·期 3
·1520-1529
·
IF 1.134
Deng Senlin,Lv Guojun,Zhai Yi,Yang Zebin,Zhu Yongqiang,Li Haichao,Wang Fumin,Zhang Xubin
Highly active and stable framework Fe-doped ZSM-5 (f-Fe-ZSM-5) zeolites with different Fe contents, which were synthesized using a facile one-pot hydrothermal method, could effectively resolve the loss of iron element during the catalytic degradation of basic dyes. The successful introduction
of Fe species into the framework of ZSM-5 was confirmed by elemental mappings, Fourier transform infrared (FT-IR) spectroscopy and Ultraviolet-visible spectroscopy (UV-vis spectra). The operational parameters, such as Fe content, H2O2 concentration, reaction temperature,
types of dyes as well as the stability of the synthesized samples were extensively evaluated. It was demonstrated that the f-Fe(0.10)-ZSM-5 exhibited an efficient catalytic ability and excellent stability even after seven consecutive runs. The degradation efficiency of f-Fe-ZSM-5 for basic
dyes was higher than that for acid dye. Therefore, f-Fe-ZSM-5 zeolites may present major potential for the treatment of basic dyes waste water without adjusting the initial pH value.
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Surfaces and Interfaces
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2025
·
IF 6.3
Chunjing Shi,Menghang Wang,Zhenyu Zhang,Hongxiu Zhou,Pengfei Hu,Longhua He,Xingzhong Liu,Huaxiang Cai,Zehong Pang
Ceramic dentures differ from those produced by additive manufacturing, and manual polishing is employed for ceramic dentures due to their hard-brittle nature, complex shapes, and thin-walled structures with thicknesses less than 1.0 mm. This presents challenges for the medical and manufacturing industries. To address these challenges, we prepared a novel ternary composite of Fe 3 O 4 @TiO 2 @PB (Prussian blue) to establish a photo-Fenton system. This composite enhances the transport of photogenerated electrons and facilitates the generation of radicals, demonstrating high photocatalytic activity for the polishing and degradation of pollutants without the need for sacrificial agents. Meanwhile, Fe 3 O 4 @TiO 2 @PB was utilized to develop a new photocatalytic magnetorheological polishing slurry. The slurry consisted of sorbitol, hydrogen peroxide, Fe 3 O 4 @TiO 2 @PB, and ceria (0.025 wt. %). After polishing, the surface roughness (Sa) decreased from 5.538 to 0.081 μm, representing a reduction of 98.54 % compared to the pristine surface. Due to photogenerated hydroxyl radicals, the Si-OH and Li-OH bonds can be created on the surface of the ceramic dentures, facilitating defects removal. Before and after polishing, the ceramic dentures enhanced the inhibition rates of Escherichia coli and Staphylococcus aureus from 50 % to 74 % and from 49 % to 80 % over the course of one day, respectively. Through irradiation with simulated sunlight, Fe 3 O 4 @TiO 2 @PB generates electrons, holes, and hydroxyl radicals, leading to the degradation of amoxicillin (AMOX) and polysorbate (PS20) by up to 99 % within 60 min. Additionally, Fe 3 O 4 @TiO 2 @PB was successfully separated and reused from the developed slurry. Therefore, the designed and developed novel ternary composite, Fe 3 O 4 @TiO 2 @PB, achieves photocatalysis, photodegradation, and recycling, offering new solutions for the medical, manufacturing, and environmental industries.
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ACS Applied Nano Materials
·
2025
·
IF 5.5
Yue Cao,Xin Zhang,Bo Ren,Xiaodong Yang
Due to the complex physiological and pathological barriers in tumor tissues, the penetration depth of light is limited and the accumulation and distribution of photosensitizers in the tumor are insufficient, which seriously affects the therapeutic effect of photothermal therapy (PTT) on solid tumors. The preparation process of traditional photothermal agents is complicated, and their biosafety needs further improvement. Moreover, photothermal agents are difficult to rapidly excrete from the body after realizing the therapeutic function, which may cause long-term potential harm to the body. In this study, multifunctional nanoparticles (FeCNPs) consisting of iron(III), curcumin, and poly(ethylene glycol) grafted polyglutamate (PLG-g-mPEG) were obtained through a simple one-pot method. The synthesized FeCNPs exhibited an average hydrodynamic size of 125 nm and a polydispersion index (PDI) of 0.462. Furthermore, the nanoparticle has excellent biocompatibility and a photothermal effect. After the PPT, the FeCNPs break down into harmless elements via a dynamic disassembly mechanism triggered by deferoxamine mesylate (DFO), facilitating swift elimination and preventing possible long-term toxicity to major organs. The therapeutic synergies enable efficient tumor removal. In summary, this study demonstrates an approach for the dynamic disassembly of metal-polyphenol nanoparticles, effectively addressing the challenge of balancing the EPR effect and renal clearance.
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SEPARATION AND PURIFICATION TECHNOLOGY
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2025
·
IF 9
Zhengming He,Cong Li,Jingzhen Su,Kai Zhang,Jiaxue zhu,Ren Cai,Yunshu Zhang,Jieming Yuan,Xiaohong Guan
Iron-based catalysts are generally used to activate oxidizing species, such as hydrogen peroxide by increasing homogeneous active substances like free radicals, to promote the degradation of organic matter. However, less attention has been paid to the reactions on the surface or the generation of heterogeneous metal-oxo species. Herein, oxygen vacancies (Vo) were introduced into Fe oxides by a calcination-induced hetero-atom doping modification. The characteristic peak of the heterogeneous hypervalent iron-oxo [≡Fe IV =O] species in the UV–Vis spectrum at 371 nm was observed. In the context of electrochemical experiment, Vo-rich Mn-Fe 2 O 3 significantly enhanced the electron conduction of sulfamethoxazole and H 2 O 2 , while simultaneously inhibiting the self-decomposition of potassium ferrate (Fe(VI)). Regarding the H 2 O 2 generated during the self-decomposition process of Fe(VI), Vo-rich Mn-Fe 2 O 3 can accelerate the degradation of sulfamethoxazole, increasing the reaction rate to 0.1081 min −1 (with a 30.05 % improvement in removal efficiency). Density functional theory calculations indicate that Vo leads to an enhanced capture of O atoms by the low-coordinated Fe atoms, promoting the anchoring of H 2 O 2 and the formation of the active ≡Fe IV =O with a higher spin state. This work proposes heterogeneous reactive species on the surface of metal oxidase, constructing Vo as the O atom capture sites in iron-based oxides to facilitate the formation of ≡Fe IV =O and the degradation of organic compounds.
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DRUG DELIVERY
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2025
·
IF 8.1
Jinguo Li,Yuhao Zhang,Changyu Shao,Yining Bai,Puxiu Wang,Tianyang Ren
Triple-negative breast cancer (TNBC) is the most aggressive type of breast cancer and is characterized by high invasiveness, rapid recurrence, and poor prognosis. To date, the ferroptosis-combined therapies have exerted their potential in the TNBC treatments via multi-mechanisms. Here, we reported a doxorubicin (DOX)–Fe complex and RSL3 co-loaded liposomes (DOX–Fe/RSL3@LIPs) for ferroptosis-enhanced chemotherapy on TNBC tumors. This nanoformulation performed a uniform spherical structure with a mean particle size of 126.9 nm, a zeta potential of −3.56 mV, and high colloidal stability. The pH-responsive dissociation of DOX–Fe and release of DOX were conducive to drug accumulation in the tumor microenvironment and tumor cells, meanwhile efficiently suppressed free DOX leakage in the blood circulation, potentially reducing the cardiotoxicity of DOX. In vitro cell and in vivo pharmacodynamic studies demonstrated a favorable anticancer effect of the DOX–Fe/RSL3@LIPs on 4T1 tumors by synchronously delivering biologically active DOX, Fe2+, and RSL3 to the tumor sites. DOX induced tumor cell death through a dual pathway of apoptosis/ferroptosis, and promoted the H2O2 generation. The tumor cell ferroptosis was observably enhanced via supplements of the ferrous ions and H2O2, and RSL3-derived GPX4 inhibition to severely destroy the oxidation balance in cells. In this paper, the DOX–Fe/RSL3@LIPs have exerted a synergistic anticancer effect on TNBC by combining ferroptosis and conventional chemotherapy, and made a meaningful exploration of new strategies for TNBC therapy.
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高影响因子
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
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2025
·
IF 8.3
Yanru Yin,Qi Xiao,Wenying Zhang,Kai Li,Dong Yan,Jian Li,Lichao Jia
Cathode materials greatly govern the performance of protonic ceramics fuel cells (PCFCs), and development of suitable cathodes for PCFCs now becomes important. In this study, the traditional proton conductor BaZrO 3 is tailored with Sr and Fe elements, aiming to design proper cathodes for PCFCs. The structural, electronic, and catalytic effects of dual-element doping on BaZrO 3 -based materials are systemically investigated. Experimental and computational analyses reveal that a 75 % iron doping concentration (BaZr 0 · 25 Fe 0 · 75 O 3 ) markedly enhances oxygen vacancy concentration, reduces proton migration barriers, and elevates electrical conductivity. Notably, moderate strontium doping (50 %) synergistically improves performance, whereas excessive doping (75 %) induces adverse effects on oxygen vacancy concentration, proton migration, and electrical conductivity. The optimized Ba 0 · 5 Sr 0 · 5 Zr 0 · 25 Fe 0 · 75 O 3 cathode achieves a peak power density of 945 mW cm -2 at 700 °C. These findings elucidate the interplay between dopant elements, doping concentrations, and material properties related to electrochemical performance, offering actionable strategies for designing high-performance PCFC cathodes.
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JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY
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2014
·
IF 2.063
Jianrong Li,Jinsheng Chen,Yanke Yu,Chi He
The Fe–Mn–Ce/CP catalyst prepared by the incipient-wetness impregnation method was investigated for elemental mercury (Hg 0 ) removal in simulated coal-fired flue gas . The incorporation of Fe could remarkably enhance the SO 2 -resistance of Fe–Mn–Ce/CP catalyst at low temperature, and the existence of water vapor had negative impact on Hg 0 removal efficiency. More than 95% of Hg 0 could be removed at 100 °C under the conditions of 60 ppm HCl, 3% O 2 ( v/v ), 5% H 2 O ( v/v ) and 400 ppm SO 2 . Hg-TPD results indicated that Hg 0 adsorption amount decreased after the addition of H 2 O or SO 2 . The XPS results revealed that the incorporation of Fe could enhance the contents of high valence Mn x + (i.e., Mn 3+ /Mn 4+ ) and Ce 3+ species in the composite catalysts, which are favorable for the oxidation process of elemental mercury. The surface characteristics were not the primary factor determining the catalytic activity . Overall, the catalytic performance of the Fe–Mn–Ce/CP catalyst was closely related to the Fe 3+ state, high ratios of (Mn 4+ + Mn 3+ )/Mn 2+ and high content of not fully coordinated cerium species.
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ENVIRONMENTAL SCIENCE & TECHNOLOGY
·
2020
·
IF 7.864
Tian Tian,Ke Zhou,Yu-Sheng Li,Dong-Feng Liu,Han-Qing Yu
Phosphorus (P) recovery from wastewater can be completed by iron-involved autotrophic denitrification via forming Fe(III)–P precipitates and/or adsorbing P onto Fe(III) oxyhydroxides. However, so far, most studies focused on the final P-containing products, while the P-capturing pathways in such a process remain unclear. In this work, autotrophic iron-dependent denitrification (AIDD) was used as a typical anoxic iron-involved P-capturing biosystem to investigate the main P recovery pathways. The AIDD biosystem showed a relatively stable capability of capturing P coupled with nitrate reduction. Direct formation of amorphous Fe(II)–P precipitates after the phosphate was fed, followed by microbially driven oxidation into Fe(III)–P minerals, was found to be the primary pathway for the P capture. In addition, adsorption of phosphate onto the formed iron oxyhydroxides also contributed to the P recovery. This work provides better understanding about recovering P in AIDD and iron-involved denitrification and highlights the important roles of iron oxidizers in the iron-related biological wastewater treatment processes.
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高影响因子
Materials Today Energy
·
2017
·
IF 0
Ge Ma,Zhen Chen,Zhihong Chen,Mingliang Jin,Qingguo Meng,Mingzhe Yuan,Xin Wang,Jun-Ming Liu,Guofu Zhou
In this work, we have prepared a series of efficient visible-light-driven WO 3 /Fe(III) nanofiber photocatalysts by electrospinning and impregnation method. The physical and optical properties of the prepared photocatalysts were characterized by field emission scanning electron microscope (FESEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and the nitrogen adsorption analysis. Under the irradiation of visible light , all the prepared WO 3 /Fe(III) nanofiber photocatalysts exhibit much higher activity for degrading methyl orange (MO) solution than the pristine WO 3 nanofibers, and reaches 94.6% under visible light irradiation for 3 h when the relative grafting amount of Fe(III) ions was 0.003 by mass percentage. Grafting of Fe(III) ions on the surface of WO 3 nanofiber could enhance its visible-light absorption and reduce the photo-generated electron-hole pairs recombination due to the interfacial charge transfer (IFCT) effect, and thus improve its photocatalytic activity , which were further verified by the ultraviolet–visible diffuse reflectance spectroscopy (UV–Vis DRS), photoluminescence (PL) and the ns-level time-resolved fluorescence decay spectrum measurements.
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ACS Applied Materials & Interfaces
·
2023
·
IF 9.5
Kunli Song,Kaiyu Guo,Yixuan Lv,Dandan Ma,Yonghong Cheng,Jian-Wen Shi
Selective catalytic reduction with ammonia is the mainstream technology of flue gas denitration (de-NOx). The reducibility and acid site are two important factors affecting the de-NOx performance, and effective regulation between them is the key to obtain a highly efficient de-NOx catalyst. Herein, a series of Mn–Fe–BTC with different ratios of Mn and Fe are synthesized, among which 2Mn-1Fe-BTC with 2:1 molar ratio of Mn and Fe has excellent low-temperature (LT) de-NOx performance (above 90% NO conversion between 60 and 270 °C) and good tolerance to H2O and SO2 poisoning (88% NO conversion at 150 °C with 100 ppm of SO2 and/or 6% H2O). It is revealed that the reducibility properties and acid sites of Mn–Fe–BTC can be flexibly tuned by the ratio of Mn and Fe. The difference in electronegativity between Fe and Mn leads to the redistribution of valence electrons, which enables the controllable reducibility of Mn–Fe–BTC. Furthermore, different amounts of Mn and Fe lead to different electron transport, which determines the type and number of acid sites. The synergistic effect of Mn and Fe endows Mn–Fe–BTC with enhanced surface molecular adsorption capacity and enables the catalyst to selectively chemisorb NH3 and NO at different active sites. This research provides guidance for the flexible regulation of reducibility and acid site of LT de-NOx catalyst.
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
·
2016
·Vol. 27
·期 6
·6382-6388
·
IF 1.798
Wang Yuxuan,Liang Weizheng,Huang Wen,Gao Min,Zhang Yin,Lin Yuan
Fe-doped BaTiO 3 thin films were grown on (001) oriented LaAlO 3 substrates using a polymer-assisted deposition technique. The microstructural and chemical state characters of the films with the Fe doping range from 1 to 10 at% were systematically investigated by X-ray diffraction and X-ray photoelectron spectroscopy. Evolution of the preferred orientation and strain status of BaTiO 3 films could be observed with increasing doping amount of Fe. Meanwhile, UV–Vis spectra of doped BaTiO 3 thin films showed that the band gap could be strongly affected by the doping amount of Fe with the smallest value at the Fe doping rate of 3 at%, which is proposed to be associated with the inevitable oxygen vacancies and the substitution of Ti ions by the Fe dopants.
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