CHEMICAL ENGINEERING JOURNAL
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2024
·
IF 13.3
Xingyu Wu,Tiantian Feng,Xiaohong Zhu,Dong Dong,Qinxue Gao,Shufan Huang,Rui Huang,Dong Wang,Huayu Xiong,Zigong Wei,Yong Chen,Jichao Liang
Pharmacological treatments of diabetic ulcers remain a huge challenge due to the impaired angiogenesis and uncontrolled bacterial infection. Here, iminopyrazine-based Fe-covalent organic frameworks (Fe-COF) were synthesized via a subcomponent assembly strategy, and functionalized through covalent modification of L-arginine and encapsulated with photosensitizer IR780 and hyaluronic acid for enhancing diabetic wound healing. The functionalized Fe-COF (Fe-COF NRs) showed peroxidase-like activity and near-infrared (NIR)-controlled NO generation property, which can be used for synergistic photothermal/photodynamic antibacterial therapy and NO-based gas therapy. Treatment with Fe-COF NRs + NIR caused pathogenic elimination and enhanced angiogenesis, subsequently leading to accelerated wound healing in a rat model of infected diabetic wound. Mechanistically, the results from RNA sequencing analysis indicated that Fe-COF NRs treatment significantly induced the expression of genes involved in angiogenesis, but obviously inhibited the expression of proinflammatory cytokines. Gene Ontology enrichment and Kyoto Encyclopedia of Genes and Genomes pathway analysis revealed that collagen-containing extracellular matrix, hair follicle development, PI3K-Akt signaling pathway, wound healing and skin development were significantly enriched after Fe-COF NRs treatment. Taken together, Fe-COF NRs provide a novel therapeutic strategy for the treatment of infected diabetic wound.
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GREEN CHEMISTRY
·
2024
·Vol. 27
·期 1
·133-143
·
IF 9.3
Hongjiao Chen,Kewei Zhang,Yanzhi Xia,Jian Li,Bin Hui
Coupling the urea oxidation reaction (UOR) and hydrogen evolution reaction (HER) in seawater is desirable to produce sustainable and green hydrogen due to the reduced energy consumption. However, developing high-performance UOR/HER electrocatalysts in seawater instead of pure water remains a great challenge. Herein, (B,P,Co,Fe)-Ni anchored on Paulownia Wood (PW) is proposed to enhance the overall urea-(sea)water splitting performance. The resulting sample only needs a potential of 1.34 V to deliver a large current density of 100 mA cm−2 for alkaline UOR and features a remarkable durability to maintain 100 mA cm−2 for 100 h. The HER and UOR (HER||UOR) coupled system in alkaline seawater-urea electrolyte for producing H2 demonstrated a more significantly reduced electrolyzer voltage of 1.67 V obtained at 100 mA cm−2 in comparison to that of the HER||OER system (1.98 V). The well-aligned micro-channels and nanopores in wood frameworks not only improve the hydrophilicity and aerophobicity of the whole electrode, which is conducive to the penetration of the electrolyte and release of bubbles, but also shorten the transmission distance of ions and intermediates to accelerate the reaction kinetic process. Density functional theory calculations reveal that Co, Fe, P and B co-doping in Ni effectively adjusts the electronic structure, and the adsorption/desorption behavior of the urea reaction intermediates is regulated by the synergistic effect from multiple components, resulting in an excellent catalytic activity in seawater-urea media. This work promotes a better understanding of the surface electronic structure modulation of nanowood via doping strategy and offers great potential in the design of advanced UOR/HER catalysts for hydrogen production and urea wastewater treatment.
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IEEE SENSORS JOURNAL
·
2024
·Vol. 24
·期 22
·36239-36246
·
IF 4.3
Dong Zhao,Honglie Chen,Kun Yang,Haoyu Wang,Xing Guo,Yang Ge,Xiushan Dong,Shengbo Sang
The application of competitive immunoassay brings many advantages to the detection of trace biomolecules and has the potential to be applied to urine-based clinical practice. However, this type of detection method has strict requirements for secondary antibody incubation processes and analysis equipment, leading to strong demands for convenient, rapid, and inexpensive detection platforms. In this study, a mechanical competitive immunosensor (MCI) was proposed for the detection of human serum albumin (HSA) based on goat anti-rabbit @Fe2O3 magnetic beads with magnetic sensitization. With the doping of Fe2O3, the conversion layer of MCI responds more accurately and rapidly to stress. In addition, goat anti-rabbit conjugated with animated Fe2O3 nanoparticles were introduced as secondary antibodies for signal amplification. Under the synergistic effect of the magnetic force of magnetic beads and the stress caused by the specific binding of antigen and antibody, the deformation of the film was amplified, which can effectively change the conductive pathway formed by doped carbon nanotubes, resulting in a larger output electric signal. Through competitive immunoassay for HSA, a limit of detection (LOD) of 68 ng/mL was achieved, which was an order of magnitude lower than direct detection methods. With high reproducibility and stability, MCI demonstrated effectiveness in the detection of HSA at a clinically significant concentration range (0.1–
$50 \; \mu $
g/mL). Moreover, MCI showed excellent specificity and selectivity, which held promise to offer an alternative tool for clinical diagnosis of urine HSA levels in nephrotic patients.
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MICROCHEMICAL JOURNAL
·
2024
·
IF 4.9
Tian Si-Yu,Ding Zhu,Yao Mu-Lan,Liu Si-Mian,Hou Xiang-Yang,Tang Long,Yue Er-Lin,Wang Xiao,Wang Ji-Jiang
A three-dimensional UiO-67-BDA with various pore structures and abundant active binding sites is constructed, and Fe@UiO-67-BDA composites with electrochemical sensing and recognition performance were further prepared by successfully loading Fe 3+ ions. The different modified electrodes (Fe@UiO-67-BDA/GCE, UiO-67-BDA/GCE, Fe/GCE) and the bare electrode (GCE) were also characterized in terms of basic structure and electrochemistry, and it was found that the basic structure and electrochemical performances of Fe@UiO-67-BDA/GCE were better than those of the remaining three electrodes, with good selectivity, reproducibility and stability. And the Fe@UiO-67-BDA/GCE sensor with good electrochemical performance was constructed under the optimal working potential (E pa = 0.59 V) and experimental conditions, which was utilized to rapidly and accurately detect heavy metal ions Hg 2+ by the DPV method, with a detection limit of up to 1.642 × 10 −9 M. In addition, the electrochemical behavior mechanism of the Fe@UiO-67- BDA/GCE sensor was investigated. Finally, the sensor was applied to detect cosmetic heavy metal ions, and the experimental results also showed high reliability and practicality. Therefore, MOFs composite material is applied to the field of electrochemistry, because of its simple operation technology, fast detection speed and high sensitivity, so that it has a greater application prospect.
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CHEMICAL ENGINEERING JOURNAL
·
2017
·
IF 6.216
Xiang Zhang,Xiaogang Gu,Shuguang Lu,Mark L. Brusseau,Minhui Xu,Xiaori Fu,Zhaofu Qiu,Qian Sui
The enhancement effect of an environmentally friendly reducing agent, ascorbic acid (AA), on trichloroethene (TCE) degradation by Fe(III)-activated calcium peroxide (CP) was evaluated. The addition of AA accelerated the transformation of Fe(III) to Fe(II), and the complexation of Fe(III)/Fe(II) with AA and its products alleviated the precipitation of dissolved iron. These impacts enhanced the generation of reactive oxygen species (ROSs). Investigation of ROSs using chemical probe tests, electron paramagnetic resonance (EPR) tests, and radical scavenger tests strongly confirm large production of hydroxyl radicals (HO ) that is responsible for TCE degradation. The generation of Cl − from the degraded TCE was complete in the enhanced CP/Fe(III)/AA system. The investigation of solution matrix effects showed that the TCE degradation rate decreases with the increase in solution pH, while Cl − , SO 4 2− and NO 3 − anions have minor impact. Conversely, HCO 3 − significantly inhibited TCE degradation due to pH elevation and HO scavenging. The results of experiments performed using actual groundwater indicated that an increase in reagent doses are required for effective TCE removal. In summary, the potential effectiveness of the CP/Fe(III)/AA oxidation system for remediation of TCE contaminated groundwater has been demonstrated. Additional research is needed to develop the system for practical implementation.
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APPLIED CATALYSIS B-ENVIRONMENTAL
·
2024
·
IF 20.2
Ruonan Guo,Changsheng Guo,Zenghui Bi,Heng Zhang,Ningqing Lv,Beidou Xi,Guangzhi Hu,Jian Xu
A novel iron-based single-atom catalyst (Fe SAC) integrated into a catalytic membrane was developed for peroxymonosulfate (PMS) activation and organic pollutant degradation. The Fe SAC membrane was synthesized using a co-precipitation method and acid leaching treatment, and its catalytic activity was evaluated in a continuous flow-through system using nitenpyram (NPR) as a model pollutant. The Fe SAC membrane/PMS system achieved over 90% NPR removal efficiency with low iron leaching (2.85–8.05 μg/L) during 10 hours of continuous operation, and maintained over 80% NPR removal in tap water, Yellow River water, and Yangtze River water. Experimental and theoretical analyses revealed that the strong chemisorption and electron transfer between PMS and FeN4 led to the dominant production of singlet oxygen for NPR degradation. This study demonstrates the potential of SAC-based catalytic membranes for efficient and stable attenuation of refractory organic pollutants in water treatment applications.
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LANGMUIR
·
2024
·
IF 3.7
Zeqi Wu,Feng Niu,Wenhao Yao,Siyuan Gao,Da Chen,Yuexiang Huang
The activation of an inert C(sp3)–H bond in selective oxidation of hydrocarbons under mild conditions is a critical and challenging process. Herein, we report a stable chlorine-coordinated metal–organic framework (MOF) photocatalyst, MIL-101(Fe), for efficient visible-light-driven photocatalytic selective oxidation of toluene to benzaldehyde in air under ambient conditions. Encouragingly, a benzaldehyde formation yield of 3.11 mmol·g–1·h–1 with a selectivity of 92.1% is achieved in 5 h, which is superior to most of the reported works. Based on the experimental results and characterizations, the high catalytic performance is mainly due to the promoted rate-limiting step of C(sp3)–H bond activation by a chlorine radical (Cl·) from the coordinated −Cl in the MIL-101(Fe) structure. In addition, the present photocatalyst possesses good substrate tolerance for photocatalytic selective oxidation of various toluene derivatives under optimized conditions.
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ELECTROCHIMICA ACTA
·
2024
·
IF 5.5
Xiaoyi Chen,Jie Yang,Kai Zhou,Zhenlong Lei,Xia Zhao,Jianqiang Zhang,Heming Luo
Supercapacitors , as an eco-friendly energy storage system, have garnered significant interest due to distinct charging/discharging mechanisms, superior power density, and robust cycle stability. This study introduces a novel approach to enhance the typically low energy density of carbon materials . By employing ferrocene (Fc) as a dopant and utilizing an external crosslinker technique for “knitting”, we synthesized Fe-doped hypercrosslinked poly(naphthalene-based) polymer MON-Fe. This polymer served as a precursor for generating Fe-doped microporous carbon, termed MONC-Fe-800–1, through a chemical activation process. Comparing the structural features of MON-Fe and MONC-Fe-800–1, microporous carbon MONC-Fe-800–1 has a more pronounced hierarchical pore structure with higher microporosity (accounting for 81.43 % of its structure) and specific surface area (819.42 m 2 g − 1 ). In a 6 M KOH electrolyte, the specific capacity of MONC-Fe-800–1 was observed to be 264.8 C g − 1 at a current density of 1.0 A g − 1 , which is much higher than the specific capacity of MON-Fe (131.9 C g − 1 ). A MONC-Fe-800–1//MONC-800–2 hybrid supercapacitor (HSC) device was constructed with an energy density of 15.2 Wh kg −1 at a power density of 750.0 W kg −1 . Notably, after 5000 charge-discharge cycles at 1.0 A g − 1 , the device maintained 83.16 % of its initial capacity with 99.92 % coulombic efficiency, which compares with 63.87 % capacity retention and 84.00 % coulombic efficiency obtained by MON-Fe//MONC-800–2 HSC, highlighting the Fe-doped microporous carbon's enhanced electrode material potential compared to its precursor.
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Advanced Healthcare Materials
·
2025
·
IF 9.6
Xianyu Zhu,Lingli Gao,Yanbo Zheng,Peng Fei Zhao,Hanrui Wei,Ruixue Liu,Liping Zhao,Junyi Zhang,Qi Sun,Lingling Zheng,Han Lv,JiGang Yang,Jianhua Gong,Zhenchang Wang
Poor prognosis and chemotherapy response stem from difficulties in precise targeting and the lack of effective synergistic treatments. Nanozymes show promising potential in tumor chemodynamic therapy (CDT) by catalyzing hydrogen peroxide (H₂O₂) decomposition and glutathione depletion in the tumor microenvironment (TME). However, integrating precise chemotherapy targeting with CDT remains challenging. In this study, a porous Fe/Cu bimetallic nanozyme carrier (FeCuNPs) is developed for co-loading with the humanized 3F8 anti-GD2 disialoganglioside antibody (3F8) and the novel pyridazinone-based chemotherapeutic agent (IMB), forming a nanoreactor (3F8@FeCuNPs@IMB) for targeted chemotherapy and CDT. The nanoreactor responds specifically to the acidic TME as a primary insurance, allowing for the controlled release of IMB at the tumor site. The targeting antibody 3F8 coating on the surface of the nanozyme carrier acts as a secondary insurance, minimizing chemotherapy drug leakage during the delivery process and ensuring precise targeting for effective chemotherapy. Furthermore, FeCuNPs act as peroxidase-like (POD) and glutathione oxidase-like (GSHOX) enzymes, catalyzing hydroxyl radical (•OH) generation and depleting excess GSH, enhancing CDT. The results in vitro and in vivo indicate that the dual insurance designed 3F8@FeCuNPs@IMB offers a promising prospect for a targeted, precise, and effective combination of chemotherapy and CDT against melanoma.
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高影响因子
DALTON TRANSACTIONS
·
2024
·Vol. 53
·期 6
·2526-2533
·
IF 3.5
Jia-Min Lyu,Shen Yu,Zhan Liu,He-You Du,Ming-Hui Sun,Chun-Mu Guo,Yi-Long Wang,Yu Li,Li-Hua Chen,Bao-Lian Su
Excessive emission of CO2 into the atmosphere has severely impacted the global ecological environment. Converting CO2 into valuable chemicals and fuels is of great significance for sustainable development. However, low activity and undesirable selectivity often result from the inherent inertness of CO2. Herein, K- or/and Zn-modified Fe-based catalysts were prepared by an incipient-wetness impregnation method for CO2 hydrogenation via a cascade reaction. The results indicate that K species exist as K2O while Zn species exist as ZnFe2O4. In the CO2 hydrogenation pathway, K2O facilitates the adsorption of CO2 and restrains the adsorption of H2, accelerating the transformation of CO2 into C2–C4 olefins rather than paraffins while Zn species promote the dispersion of Fe species, leading to improved activity. Synergistically, a K- and Zn-modified Fe-based catalyst (2Zn–10K–Fe/Al) shows excellent catalytic CO2 hydrogenation activity, achieving a CO2 conversion of 77% which is 1.8 times that (42%) of the unmodified Fe-based catalyst (Fe/Al). Our catalyst also shows a significantly promoted selectivity to C2–C4 olefins of 17% in comparison with the Fe/Al catalyst (0%). It is envisioned that such a binary effect of elements might contribute to the low-cost and industrial production of Fe-based catalysts for selective CO2 conversion.
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SEPARATION AND PURIFICATION TECHNOLOGY
·
2024
·
IF 8.1
Shuzhuang Sun,Bocheng Yu,Yanmei Shen,Yu Liu,Hongman Sun,Xuan Bie,Mengna Wu,Yongqing Xu,Chunfei Wu,Hui Zhou
Integrated CO 2 capture and utilization (ICCU) using “capture-conversion” dual functional materials (DFMs) paves a cost-effective path for restricting CO 2 emissions by eliminating the energy-intensive intermediate processes. The interactions between catalysts and absorbents are believed pivotal in ICCU; however, there is a lack of environment-friendly strategy to fabricate the interaction for industrial applications. Here, we propose a solvent-free mechanochemical approach to promote the interaction by improving the proximity between natural calcium and iron sources. The interaction was systemically investigated and confirmed using XRD, XPS, TEM, TPR, etc. As a result, the mechanochemical approach derived DFM achieved 5.5 mmol g −1 CO 2 capacity, 87 % CO 2 conversion, and 100 % CO selectivity at 650 °C, significantly outperforming the CaO-alone benchmark (CO 2 capacity < 4.5 mmol g −1 , CO 2 conversion < 73 %). Further incorporating MgO would alleviate the sintering and promote the CO 2 capture stability (< 15 % decrease after 20 cycles) by acting as a thermal-stable barrier. Based on in situ XRD, it is further confirmed that Fe-Ca interaction exhibits a dynamic looping mechanism in ICCU. The techno-economic analysis strongly supports the superiority of ICCU catalyzed by naturally sourced DFMs on eliminating the energy and H 2 consumption for CO 2 capture and upgradation. As a result, producing CO via ICCU using mechanochemical derived DFMs exhibits 20 % and 10 % cost decrease compared to the conventional CCU and ICCU using CaO alone scenarios, pointing out the potential of ICCU technology in industrial applications.
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Journal of Water Process Engineering
·
2025
·
IF 6.7
Liping Zhang,Huitong Li,Mengnan Duan,Weiwei Wang,Ran Mu,Zehua Pi,Yubin Shang
Coking reverse osmosis concentrates (ROCs) are characterized by a high organic content, complex composition, and difficulty in biological degradation. To achieve the zero liquid discharge (ZLD) strategy, ROCs need to be treated urgently. This work aims to prepare a modified catalyst under high-efficiency activated alumina (γ-Al 2 O 3 ) loaded with Fe and Co bimetals and to degrade m-cresol as a typical pollutant in actual coking ROCs. The results showed that Fe and Co metals were successfully loaded. Meanwhile, the catalyst enhances the reactive active sites, reduces the activation energy of the reaction, and improves the degradation efficiency. The degradation mechanism and removal process were investigated. The results showed that with the optimal conditions, as ozone dosage of 50 mg/L, gas flow rate of 400 mL/min, catalyst dosage of 30 g/L, and pH value of 9, the removal rates of COD, TOC, and UV 254 were 75.61 %, 56.22 %, and 84.14 %, respectively. This study provides a better treatment option for the degradation of m-cresols in coking ROCs.
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