Journal of the Taiwan Institute of Chemical Engineers
·
2018
·
IF 3.849
Weirui Chen,Zulin Zhang,Xukai Li,Dan Wu,Ying Xue,Laisheng Li
Fe-Cu-MCM-41/O 3 was first used as an alternative to O 3 to control disinfection by-products generation from chlorinated-disinfection of Br-containing Diclofenac. Accompanying with decrease of TOC , THMs and HAAs had an initial increase, reaching the highest at 30 min, then gradually decreased. Coupling Fe-Cu-MCM-41 with O 3 successfully enhanced TOC removal and inhibited bromate, THMs and HAAs formation in post-chlorination when compared with those in ozonation . Four kinds of THMs and six kinds of HAAs were detected. CHCl 3 was main Cl-THMs and CHBrCl 2 was main Br-THMs. CHCl 2 COOH was the dominant Cl-HAAs and CHClBrCOOH was main Br-HAAs. A converse Br-THMs order was observed in O 3 and Fe-Cu-MCM-41/O 3 pre-treatment. Fe-Cu-MCM-41 decreased ozone exposure, reducing the direct reaction of O 3 with Br − to form bromate. More DBPs precursors in Fe-Cu-MCM-41/O 3 were removed by ·OH. H 2 O 2 , which generated during pre-treatment process, reduced HBrO/BrO − to Br − , inhibiting both its reaction with Br-DBPs precursors and bromate formation. The pre-treatment process changed intermediates’ properties and hydrophilic DOM was the dominant component. Hydrophobic acids and transphilic DOM were the main chlorine consuming intermediates and had major contribution to DBPs formation. Fulvic-like intermediates was suggested as precursors of Br-DBPs. Fe-Cu-MCM-41/O 3 were suggested as a good alternative to O 3 pretreatment.
研究领域:
环境科学
·
水处理工程
✓ 已验证
DOI
高影响因子
JOURNAL OF SOLID STATE ELECTROCHEMISTRY
·
2024
·Vol. 28
·期 8
·2959-2971
·
IF 2.6
Gao Yali,Pang Wanyu,Chang Xile,Hu Zhiyong,Hu Tuoping,Ma Xuemei
Baicalin (Bn) is one of the flavonoids with various biological activities, and its accurate determination is of great significance to clinical medicine. The new “MOF-on-MOF” materials have a broad application prospect. ZIF-67 and MIL-101(Fe) are typical metal–organic frame (MOF) materials, which have the advantages of flexible structure, large specific surface area, large porosity, and adjustable pore size. In this paper, a disposable and sensitive Bn electrochemical sensor based on ZIF-67/MIL-101(Fe) composite modified carbon paper (CP) electrode was developed for the first time. The sensing nanomaterials were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction spectroscopy (XRD), and X-ray photoelectron spectroscopy (XPS). Cyclic voltammetry (CV) was used to evaluate the electrochemical behavior of Bn on different modified electrodes. The results showed that ZIF-67/MIL-101(Fe)/CP exhibited a well-defined redox peak compared with bare CP, ZIF-67/CP, and MIL-101(Fe)/CP, which was attributed to the synergistic effect of ZIF-67 and MIL-101(Fe). Under optimal conditions, the electrochemical sensor was able to quantify Bn in the ranges of 0.01 ~ 3 µM and 3 ~ 6 µM with a detection limit (LOD) as low as 0.009 µM (S/N = 3). In addition, the sensor was successfully used for the quantitative analysis of Bn in Dual yellow oral liquid with reliable results.
研究领域:
分析化学
·
药物分析
·
生物医学工程
✓ 已验证
DOI
高影响因子
Energy Storage Materials
·
2020
·
IF 16.28
Chong Bai,Huijie Jin,Zongshuai Gong,Xizheng Liu,Zhihao Yuan
Aqueous Fe-I 2 rechargeable batteries are highly desirable for large-scale energy storage because of their intrinsic safety, cost effective, and wide abundance of iron and iodine. However, their development suffers from Fe dendrite growth and severe shuttle effect during cycling. Herein, we demonstrate a high-performance Fe-I 2 rechargeable battery using metal iron as anode, iodine/hierarchically porous carbon composite as cathode and an eco-friendly aqueous electrolyte. The anode modified with ascorbic acid effectively suppresses the formation of iron dendrite, while the cathode doped with nitrogen greatly reduces the shuttle of iodine species. The battery operates a reversible redox reaction of FeI 2 /I 2 pair with fast kinetics. A capacity ~190 mAh g -1 at current densities up to 5000 mA g -1 and excellent cycle stability of 100% after 550 cycles at 2000 mA g -1 are obtained. The battery achieves superior power density of ~1300 W kg -1 at 120 Wh kg -1 and high energy density of 130 Wh kg -1 at 356 W kg -1 . Our study shows great promise for high-performance rechargeable batteries with low-cost, eco-friendliness and high safety.
研究领域:
能源存储
·
电池技术
·
材料科学
✓ 已验证
DOI
高影响因子
Environmental Science-Advances
·
2023
·Vol. 2
·期 5
·731-739
·
IF 0
Wen Wen,Yina Liu,Zhongping Li,Guangming Wen,Hung-Wing Li,Li Li
In this study, we report a simple pyrolytic strategy for N–C co-doped Fe-based nanoparticles (Fe–N–C) and exhibit their oxidase-mimicking and peroxidase-mimicking activity in a chromogenic reaction with 3,3′,5,5′-tetramethylbenzidine dihydrochloride (TMB) as a substrate. Structural analysis revealed that Fe–NX and Fe3C structures were formed with Fe-Imace coordination compounds as precursors and melamine as the nitrogen source, which provided abundant active sites for the Fe–N–C nanozyme. Interestingly, owing to the blocking effect triggered by π–π stacking between the tetracycline antibiotics (TCs) tetraphenyl skeleton and Fe–N–C, the substrate affinity of the Fe–N–C was significantly blocked, resulting in the solution fading. Under the optimum conditions, the UV absorption intensity versus the concentration of TCs was found to be linear over the range of 0.08–90 μM for tetracycline (TC), 0.1–80 μM for chlortetracycline (CTC) and 0.09–100 μM for oxytetracycline (OTC). The detection limits were 62 nM for TC, 85 nM for CTC and 88 nM for OTC. The Fe–N–C displayed good storage and long-term stability when stored at 4 °C for 30 days. In addition, based on its superparamagnetism, Fe–N–C can be effectively recycled and reused through an external magnetic field, avoiding secondary pollution.
研究领域:
分析化学
·
生物医学工程
·
环境科学
✓ 已验证
DOI
Journal of Environmental Chemical Engineering
·
2025
·
IF 7.2
Mingrui Geng,Zhizhen Wang,Denghui Wang
Formaldehyde (HCHO), a ubiquitous indoor organic pollutant, severely threatens human health. Developing efficient and low-energy catalytic materials for room-temperature HCHO purification remains an urgent priority. In this work, Fe y MnO x catalysts were synthesized via a facile coprecipitation method. The Fe doping effectively modulated the morphology and crystallinity of δ-MnO 2 while inducing the formation of surface oxygen vacancies, thereby enhancing the capability to generate surface reactive oxygen species. Under a gas hourly space velocity (GHSV) of 150 L·g cat –1 ·h –1 , the catalyst achieved > 99 % removal efficiency for 100 ppm HCHO, along with exceptional stability. In situ DRIFTS reveals the influence of Fe doping on the catalytic reaction pathway for HCHO. This work demonstrates that the Fe doping strategy successfully optimizes the microstructure and surface chemical properties of δ-MnO 2 , resulting in outstanding room-temperature HCHO removal performance, providing valuable insights into defect engineering for optimizing transition metal oxide catalysts.
研究领域:
环境催化
·
材料科学
·
室内空气净化
·
过渡金属氧化物
·
缺陷工程
✓ 已验证
产品关联
DOI
高影响因子
DALTON TRANSACTIONS
·
2021
·Vol. 50
·期 46
·17265-17274
·
IF 4.39
Yun-Wu Li,Shi-Kun Su,Cai-Zhen Yue,Jun Shu,Peng-Fang Zhang,Fang-Hui Du,Su-Na Wang,Hui-Yan Ma,Jie Yin,Xin Shao
Electrochemical water splitting is convinced as one of the most promising solutions to combat the energy crisis. The exploitation of efficient hydrogen and oxygen evolution reaction (HER/OER) bifunctional electrocatalysts is undoubtedly a vital spark yet challenging for imperative green sustainable energy. Herein, through introducing a simple pH regulated redox reaction into a tractable hydrothermal procedure, a hierarchical Fe3O4@MnOx binary metal oxide core–shell nano-polyhedron was designed by evolving MnOx wrapped Fe3O4. The MnOx effectively prevents the agglomeration and surface oxidation of Fe3O4 nano-particles and increases the electrochemically active sites. Benefiting from the generous active sites and synergistic effects of Fe3O4 and MnOx, the Fe3O4@MnOx-NF nanocomposite implements efficient HER/OER bifunctional electrocatalytic performance and overall water splitting. As a result, hierarchical Fe3O4@MnOx only requires a low HER/OER overpotential of 242/188 mV to deliver 10 mA cm−2, a small Tafel slope of 116.4/77.6 mV dec−1, combining a long-term cyclability of 5 h. Impressively, by applying Fe3O4@MnOx as an independent cathode and anode, the overall water splitting cell supplies a competitive voltage of 1.64 V to achieve 10 mA cm−2 and super long cyclability of 80 h. These results reveal that this material is a promising candidate for practical water electrolysis application.
研究领域:
材料科学
·
能源化学
✓ 已验证
DOI
PubMed
高影响因子
BIOMATERIALS
·
2013
·
IF 7.604
Shuai Xu,Jing Liu,Dian Li,Liming Wang,Jia Guo,Changchun Wang,Chunying Chen
We propose a modular synthetic strategy to constitute metallosalphen prodrugs in the form of coordination polymer nanoparticles , comprising magnetite nanocrystal colloidal cluster as core and salphen-In III coordination polymer as shell. These composite nanoparticles are not only equipped with intense photoluminescence , sensitive magnetic responsiveness and pH-dependent degradability, but also serve as prodrugs to accomplish intercellular conversion from non-toxic nanoparticles (Fe 3 O 4 @Salphen-In III ) to pharmacologically active complexes (Fe–salphen), allowing to specifically inhibit the proliferation of A549 cancer cells via caspase activation.
研究领域:
材料科学
·
生物医学工程
·
肿瘤学
✓ 已验证
DOI
PubMed
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2025
·
IF 9.7
Yaping Zhang,Yanan Zhao,Yixin Qi,Yanyan Lin,Yuhang Cheng,Mengmeng Sun,Lei Wang
Photogenerated holes have emerged as critical mediators for activating peroxymonosulfate (PMS) in the coupled photocatalytic PMS activation system, enabling novel dual-channel activation pathway. A tandem system based on Fe-MOF@BiVO 4 (Vis/PMS/Fe-MOF@BVO) with spatially separated active sites was constructed to form a dual-channel activation mechanism. The BiVO 4 (010) face provides the active sites for photogenerated electrons to drive the Fe 3+ /Fe 2+ cycle and activate PMS, while the BiVO 4 (110) face serves as the active sites for photogenerated holes to activate PMS. Consequently, the Vis/PMS/Fe-MOF@BVO system achieved complete degradation of 10 mg/L BPA within 6 min, with a degradation rate constant (K obs ) of 0.74 min −1 . It also demonstrated high removal efficiency for various organic pollutants with excellent immunity to interference and reusability. This work provides a new insight into the coordinative mechanism for coupled photocatalysis and PMS activation system.
研究领域:
环境科学
·
材料科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2022
·
IF 9.965
Ning Liu,Fuhao Fei,Wangxi Dai,Jianqiu Lei,Fukun Bi,Botao Wang,Guixiang Quan,Xiaodong Zhang,Liang Tang
Herein, a highly efficient Z-scheme SnS 2 /MIL-88B (Fe) (SnSFe) heterojunction was successfully synthesized to use both as photocatalysts and persulfate (PS) activator for ibuprofen (IBP) degradation. Flower-liked SnS 2 was uniformly loaded on MIL-88B (Fe), and SnSFe retained the original polyhedral morphology of MIL-88B (Fe). The highest removal of IBP was achieved in the presence of SnSFe with 0.5% SnS 2 (SnSFe0.5). Characteristic results and density functional theory calculations demonstrated that the enhanced degradation of IBP was due to the difference in Fermi energy levels of SnS 2 and MIL-88B (Fe) leading to electrons transferred from SnS 2 to MIL-88B (Fe), and Sn O bond was formed in SnSFe. , OH and O 2 − were the main active species in SnSFe0.5/PS/visible light system. Z-scheme heterojunction of SnSFe was constructed to propose the degradation mechanism. This research revealed that the synergism of photocatalysis and PS activation using SnS 2 /Fe-based MOFs composites possessed great potentials in wastewater remediation.
研究领域:
环境科学
·
材料科学
✓ 已验证
DOI
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2025
·
IF 6.3
Yuan Ma,Chunhong Li,Muhammad Aizaz Ud Din,Lan Zhao,Nengcong Pan,Yuhan Lei,Nanpu Cheng
Affordable and highly effective electrocatalysts are essential for achieving industrial-scale hydrogenation of water applications. The successful fabrication of Fe-doped CoSe 2 nanosheets supported on nickel foam (Fe x -CoSe 2 /NF) via a two-step electrochemical deposition method is presented in this study, showing their effectiveness as an electrocatalyst for the oxygen evolution reaction (OER) in water splitting. The performance of Fe x -CoSe 2 /NF initially improves with increasing x, reaching an optimal value before subsequently declining. The ideal catalyst, Fe 0.75 -CoSe 2 /NF, requires a low overpotential of 256 mV at 10 mA cm −2 , and even at 100 mA cm −2 , the overpotential remains as low as 291 mV. The catalyst also displays a low Tafel slope of 34.37 mV dec −1 , highlighting the fast OER kinetics. Furthermore, Fe 0.75 -CoSe 2 /NF demonstrates exceptional electrochemical stability. The enhanced OER catalytic performance of Fe-doped CoSe 2, compared to intrinsic CoSe 2, is attributed to the thinner nanosheets structure and optimized electronic structures, which provide a higher density of active sites and facilitate a new reaction coordination with a lower energy barrier during the OER process. These findings not only offer new mechanistic insights into Fe-doped CoSe 2 systems but also provide a scalable and cost-effective pathway for designing next-generation, non-precious-metal-based electrocatalysts.
研究领域:
电化学
·
纳米材料
·
催化
·
能量转换
·
材料科学
✓ 已验证
产品关联
DOI
高影响因子
COMPOSITES PART B-ENGINEERING
·
2025
·
IF 14.2
Chunmiao Liu,Yurun Feng,Haibin Sun,Qiangqiang Hu,Hui Xiao,Xue Guo,Huaiqing Zhang
The increasingly complex electromagnetic environment and escalating stealth technology requirements pose unprecedented challenges to multifunctional electromagnetic wave (EMW) absorbing materials. While significant progress has been made, existing SiBCN material systems still struggle to simultaneously achieve broadband absorption and strong attenuation. In response to this demand, we propose a Fe-Co-Ni ternary co-doping strategy from the perspective of multiple doping and magnetic medium coupling. By precisely controlling the content of magnetic elements, the synergistic effect between magnetic loss and dielectric loss is realized. The experimental results show that the minimum reflection loss (RL min ) of the optimized SiBCN/Fe-Co-Ni fibers reach -53.19 dB, and a broadband absorption of 5.36 GHz is achieved at a thickness of 1.98 mm. More importantly, the material maintains excellent stealth performance across a wide range of incident angles. Capitalizing on these outstanding properties, we have successfully designed a low radar cross-section (RCS) stealth antenna. The antenna exhibits a 27.5 dBsm RCS reduction at 9.24 GHz. This work not only clarifies the synergistic mechanism of multiple magnetic doping to regulate electromagnetic parameters, but also provides new ideas for the development of new generation of smart stealth materials and devices.
研究领域:
材料科学
·
电磁学
·
天线设计
·
隐身技术
✓ 已验证
产品关联
DOI
高影响因子
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2018
·
IF 4.229
Jiqiong Lian,Yihui Wu,Houan Zhang,Siyong Gu,Zhiwei Zeng,Xiaoyun Ye
Design of inexpensive and highly efficient bifunctional electrocatalyst is paramount for overall water splitting . In this study, amorphous Ni–Fe–P alloy was successfully synthesized by one-step direct-current electrodeposition method. The performance of Ni–Fe–P alloy as a bifunctional electrocatalyst toward both hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER) was evaluated in 30 wt% KOH solution. It was found that Ni–Fe–P alloy exhibits excellent HER and OER performances, which delivers a current density of 10 mA cm −2 at overpotential of ∼335 mV for HER and ∼309 mV for OER with Tafel slopes of 63.7 and 79.4 mV dec −1 , respectively. Moreover, the electrolyzer only needs a cell voltage of ∼1.62 V to achieve 10 mA cm −2 for overall water splitting. The excellent electrocatalytic performance of Ni–Fe–P alloy is attributed to its electrochemically active constituents, amorphous structure, and the conductive Cu Foil.
研究领域:
材料科学
·
电化学
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）