JOURNAL OF ALLOYS AND COMPOUNDS
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2020
·
IF 4.65
Danhua Liu,Xin Liu,Jian Wang,Xinhua Mao,Xiaochang Xu,Xi’an Fan
The effect of Fe nanoparticles with mass fraction of 0-7 wt% on the microstructure and soft magnetic properties of the Fe-6.5 wt%Si soft magnetic composites (SMCs) was investigated. The results show that the pores between Fe-6.5 wt%Si powders can be effectively filled by Fe nanoparticles , thereby correspondingly increasing the density of the SMCs. At the same time, the magnetic permeability of the SMCs mixed with different mass fraction of Fe nanoparticles has improved significantly and exhibits good frequency stability compared with the absence of Fe nanoparticles. It also reveals that the addition of 1 wt% Fe nanoparticles can reduce the eddy current loss of the SMCs by decreasing its intra-particle eddy current loss. When the addition of Fe nanoparticles is 3 wt%, the SMCs exhibits good magnetic properties with high magnetic permeability (increased by 24%) and relatively low core loss.
研究领域:
材料科学
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磁学
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DOI
高影响因子
Journal of Environmental Chemical Engineering
·
2025
·
IF 7.2
Yunpeng Zha,Xiaoxiao Sun,Zhengjun Xiong,Dandan Dong,Shili Li,Qinqin Wang,Minmin Liu
The porous carbon materials co-coordinated with Fe and N (Fe-N-C) were successfully synthesized through one-step pyrolysis with the zeolitic imidazolate framework (ZIF-8) as the precursor. Through systematic optimization of iron ion concentration during synthesis, the Fe-N-C-20 specimen exhibited optimal adsorption performance toward dibenzothiophene (DBT), demonstrating a maximum sulfur adsorption capacity of 22.14 mg S/g with a corresponding removal efficiency of 92 %. This superior performance can be primarily ascribed to the formation of Fe-S bonds anchored on Fe-N active sites, N-S interactions mediated by graphitic nitrogen species and appropriate pore size that allows access to thiophenic compounds. Furthermore, the experimental adsorption isotherms for DBT exhibited strong correlation with the Density Functional Theory (DFT) calculation. Additionally, the material's adsorption process followed pseudo-second-order kinetics and Langmuir isotherms of Fe-N-C, and the pseudo-second-order model shows the smallest RMSE (0.66), extremely low SSE (3.03) and AIC (-1.86), which further proves its excellent fitting ability. And the best balance between parameter efficiency and fitting performance. The high stability and recyclability of ZIF-derived Fe-N-C porous adsorbents contribute to sustainable industrial practices.
研究领域:
材料科学
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环境工程
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产品关联
DOI
高影响因子
Journal of Materials Chemistry A
·
2021
·Vol. 9
·期 26
·14793-14805
·
IF 12.732
Yuan Gao,Xiaoguang Duan,Bin Li,Qianqian Jia,Yang Li,Xiaobin Fan,Fengbao Zhang,Guoliang Zhang,Shaobin Wang,Wenchao Peng
Persulfate-based advanced oxidation processes are promising technologies to solve water pollution. In this work, single iron atoms are anchored on three-dimensional N-doped carbon nanosheets by a chemical vapor deposition (CVD) method with ferrocene-loaded CaO as the hard template. The high surface density of Fe–N4 sites and abundant interconnected meso–macro pores are highly favorable for activating peroxymonosulfate (PMS) to produce superoxide radicals (O2˙−), giving rise to ultrahigh activity and excellent stability for pollutant degradation. Experiment and density functional theory (DFT) calculations reveal that Fe–N4 is the main active site, on which electrons transfer from C to Fe via the C–N–Fe bond to secure the low-valence state of Fe species for the redox process. This work proposes a new strategy for developing highly active single-atom materials by CVD and reveals mechanisms of PMS activation on single-atom activators.
研究领域:
环境科学
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材料科学
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产品关联
DOI
高影响因子
CHEMOSPHERE
·
2021
·
IF 7.086
Peipei Huang,Lili Yao,Qing Chang,Yunhan Sha,Guodong Jiang,Shenghua Zhang,Zhe Li
The slow redox rate of Fe(III)/Fe(II) couples is a rate-limiting step for Fenton-like performance of Fe-MOFs. In this study, a series of catalysts (MIL-101) with various p-phthalic acid/2-aminoterephthalic acid (H 2 BDC/NH 2 –H 2 BDC) molar ratios were prepared using a simple and mild chemical method and applied for catalyzed degradation of bisphenol A (BPA). Interestingly, the –NH 2 modified MIL-101(Fe) can adjust Fe-Oxo node by increasing the electron density of Fe(III) in the presence of –NH 2 group with high electron density, thus forming Fe(II) in situ in MOFs. Meanwhile, the –NH 2 groups used as electron-donors can promote electron transfer , resulting in faster Fe(III)→Fe(II) half-reaction and active H 2 O 2 to continuously generate •OH radical. The BPA degradation and rate constant of Fe-BDC-NH 2 /H 2 O 2 system are 15.4-fold and 86.8-fold higher than that of Fe-BDC/H 2 O 2 system, respectively. The density functional theory (DFT) calculations showed that Fe-BDC-NH 2 possesses higher Fermi level energy (−4.88 eV) and lower activation energy barriers (0.32 eV) compared with Fe-BDC. Moreover, Fe-BDC-NH 2 showed good reusability and stability. This work offers a highly efficient and stable MOFs-based Fenton-like catalyst to rapidly degrade organic pollutants over a wide pH range for potential applications in wastewater treatment .
研究领域:
环境科学
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材料科学
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化学工程
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产品关联
DOI
PubMed
高影响因子
WATER RESEARCH
·
2022
·
IF 13.4
Haolin Xu,Rundong Chen,Sheng Liang,Zhenchao Lei,Wenxiao Zheng,Zhang Yan,Jianxin Cao,Chaohai Wei,Chunhua Feng
The formation of chlorinated byproducts represents a significant threat to the quality of the effluent treated using electrochemical advanced oxidation processes (EAOPs), thus spurring investigation into alleviating their production. This study presents a new strategy to minimize the release of chlorinated intermediates during the electrochemical oxidation of Ni-EDTA by establishing a dual mixed metal oxide (MMO)/Fe anode system. The results indicate that the dual-anode system achieved a substantially higher rate (0.141 min − 1 ) of Ni-EDTA destruction and accordingly allowed a more pronounced removal of aqueous Ni (from 39.85 to 0.63 mg L − 1 ) after alkaline precipitation, compared with its single MMO anode (0.017 min − 1 of Ni-EDTA removal, with 14.38 mg L − 1 Ni remaining) and single Fe anode (insignificant Ni-EDTA removal, with 38.37 mg L − 1 Ni remaining) counterparts. Compared to reactive chlorine species (RCS) produced from the single MMO anode system, Fe(IV) was in situ generated from the dual-anode system and was predominantly responsible for the attenuation of chlorinated byproducts and thus the decrease in the acute toxicity of the treated solution (evaluated using luminescent bacteria). The Fe(IV)-dominated dual-anode system also exhibited superior performance in removing multiple pollutants (including organic ligands, Ni, and phosphite) in the real electroless plating effluent. The findings suggest that the strategy for Fe(II) transition to Fe(IV) by active chlorine paves a new avenue for yielding less chlorinated products with lower toxicity when EAOPs are used to treat chloride-containing organic wastewater.
研究领域:
环境科学
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电化学工程
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产品关联
DOI
PubMed
高影响因子
WATER RESEARCH
·
2023
·
IF 12.8
Tao Yang,Linqian An,Ge Zeng,Maoju Jiang,Juan Li,Changyu Liu,Jianbo Jia,Jun Ma
The widespread occurrence of p -arsanilic acid ( p -ASA) in natural environments poses big threats to the biosphere due to the generation of toxic inorganic arsenic (i.e., As(III) and As(V), especially As(III) with higher toxicity and mobility). Oxidation of p -ASA or As(III) to As(V) followed by precipitation of total arsenic using Fe-based advanced oxidation processes demonstrated to be a promising approach for the treatment of arsenic contamination. This study for the first time investigated the efficiency and inherent mechanism of p -ASA and As(III) oxidation by Fe(II)/peracetic acid (Fe(II)/PAA) and PAA processes. p -ASA was rapidly degraded by the Fe(II)/PAA process within 20 s at neutral to acidic pHs under different conditions, while it was insignificantly degraded by PAA oxidation alone. Lines of evidence suggested that hydroxyl radicals and organic radicals generated from the homolytic O O bond cleavage of PAA contributed to the degradation of p -ASA in the Fe(II)/PAA process. p -ASA was mainly oxidized to As (V), NH 4 + , and p -aminophenol by the Fe(II)/PAA process, wherein the aniline group and its para position were the most vulnerable sites. As(III) of concern was likely generated as an intermediate during p -ASA oxidation and it could be readily oxidized to As(V) by the Fe(II)/PAA process as well as PAA alone. The in-depth investigation demonstrated that PAA alone was effective in the oxidation of As(III) under varied conditions with a stoichiometric molar ratio of 1:1. Efficient removal (> 80%) of total arsenic during p -ASA oxidation by Fe(II)/PAA process or during As(III) oxidation by PAA process with additional Fe(III) in synthetic or real waters were observed, mainly due to the adsorptive interactions of amorphous ferric (oxy)hydroxide precipitates. This study systematically investigates the oxidation of p -ASA and As(III) by the Fe(II)/PAA and PAA processes, which is instructive for the future development of arsenic remediation technology.
研究领域:
环境科学
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化学
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产品关联
DOI
PubMed
高影响因子
Catalysts
·
2023
·Vol. 13
·期 7
·1057
·
IF 3.9
Rongwei Zheng,Ruifan Tan,Yali Lv,Xiaoling Mou,Junqiao Qian,Ronghe Lin,Ping Fang,Weidong Kan
Iron-based materials are widely applied in Fenton chemistry, and they have promising prospects in the processing of wastewater. The composition complexity and rich chemistry of iron and/or oxides, however, hamper the precise understanding of the active sites and the working mechanism, which still remain highly controversial. Herein, iron oxides of four different model systems are designed through a conventional precipitation method plus H2reduction treatment. These systems feature Fe@Fe3O4with abundant oxygen vacancy, Fe0and Fe3O4particles with interface structures, and Fe3O4-dominated nanoparticles of different sizes. These materials are applied in the decomposition of methyl orange as a model reaction to assess the Fenton chemistry. The Fe@Fe3O4with core–shell structures exhibits significantly higher decomposition activity than the other Fe3O4-rich nanoparticles. A thin Fe3O4layer formed by auto-oxidation of iron particles when exposed to air can boost the activity as compared with the Fe0and Fe3O4particles with interface structures but poor oxygen vacancy. The unique hetero-structure with the co-existence of both metallic iron and oxygen vacancy displays excellent redox propensity, which might account for the superior Fenton activity. This finding provides a new perspective to understand and design highly efficient iron-based Fenton catalysts.
研究领域:
环境科学
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材料科学
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产品关联
DOI
高影响因子
JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY
·
2022
·
IF 6.76
Meng Zhang,Yu Zhang,Yucong Chen,Xiaoru Tian,Lingzhi Liu,Yizhong Wang,Ruijie Guo,Hong Yan
MIL-88(Fe) was used as an oxidant and a hard template for the synthesis of polypyrrole (PPy) on its surface, and the formation of PPy made the surface of MIL-88(Fe) rougher as well as more voids formed in the interior. The increased specific surface area allowed more benzotriazole (BTA) (17.8 wt%) loaded on PPy/MIL-88 particles. BTA/PPy/MIL-88(Fe) was employed as a novel corrosion inhibitor to enhance the corrosion resistance of epoxy coating for carbon steel. BTA/PPy/MIL-88(Fe) filler improved the corrosion resistance of EP coating without/with artificial scratch by delaying the cathodic and anodic reactions in corrosive media. Both BTA and MIL-88(Fe) played the role of corrosion inhibitors, making EP coating possess active corrosion protection and pH-sensitive performance. Besides, BTA/PPy/MIL-88(Fe) enhanced the adhesion of EP coating by filling the pores inside.
研究领域:
材料科学
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防腐蚀工程
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化学工程
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产品关联
DOI
高影响因子
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2020
·
IF 3.99
Qingwen Long,Feng Liu,Yanjie Yuan,Yuting Dai,Chunli Wang,Xuheng Li,Jing Zhang
In this study, heterogeneous Fenton-like catalyst, nano-Fe° encapsulated in hydrothermal carbon (Fe°/HTCC), was prepared via a green chemistry route, aiming at increasing the degradation efficiency of p-chlorophenol (4-CP) by controlling the stability of the catalyst and Fe(III)/Fe(II) cycling in the advanced oxidation process. The degradation of 4-CP by heterogeneous Fenton reactions was conducted with the assistance of visible light, which was monitored with the aid of the HPLC and total organic carbon analysis. The results revealed that Fe°/HTCC composite markedly enhanced both the degradation (100 %) and the mineralization efficiency (∼73.9 %) for 100 mg/L 4-CP within 60 min at pH 4.0. More importantly, the catalyst presented a high stability to resist the side oxidation, where the removal efficiency was maintained even after 5 successive cycling experiments. Electron spin resonance confirmed that in the presence of both HTCC and visible light irradiation greatly enhanced the production of •OH for the degradation and mineralization of 4-CP, which can be attributed to the enhancement of Fe(III)/Fe(II) cycling. This study paves a new way toward the rational design of Fe°–carbon composites as heterogeneous Fenton-like catalysts for potential applications into wastewater treatment.
研究领域:
环境科学
·
化学工程
·
材料科学
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产品关联
DOI
高影响因子
MOLECULES
·
2024
·Vol. 29
·期 9
·2078
·
IF 4.2
Yu Cao,Zeming Dai,Xuan Zhou,Yuting Lin,Jianhua Hou
The dyes in printing and dyeing wastewater are harmful to the human body and the environment. It is essential to develop practical and effective adsorbents to deal with them. In this study, an Fe-doped, ZIF-67 derived Fe/Co/C composite material with strong magnetism was successfully synthesized. The effects of pH, initial concentration, and adsorption time on the properties of the adsorbent were investigated. To further improve the removal efficiency and enhance the practicality, potassium peroxymonosulfate (PMS) was added to the system due to its Fenton-like effect. Then, an Fe/Co/C composite was used with PMS to remove Congo red (CR) with a 98% removal of 250 mg·L−1. Moreover, for its high saturation magnetization of 85.4 emu·g−1, the Fe/Co/C composite can be easily recovered by applying a magnetic field, solving the problem that powdery functional materials are difficult to recover and, thus, avoiding secondary pollution. Furthermore, since the composite material was doped before carbonization, this synthetic strategy is flexible and the required metal elements can be added at will to achieve different purposes. This study demonstrates that this Fe-doped, ZIF-67 derived magnetic material has potential application prospects for dye adsorption.
研究领域:
环境科学
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材料科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
APPLIED CATALYSIS B-ENVIRONMENTAL
·
2025
·
IF 21.1
Qingfei Zhao,Zhenpeng Guo,Zhuohan Wu,Shuyuan Dong,Ronghao Kang,Bingdian Jiang,Shuhui Guan,Ting Zhang,Zhenfeng Bian
The advanced oxidation process (AOP) based on hydroxyl radical ( • OH) has garnered increasing attention in water purification and wastewater treatment. However, producing • OH by activating hydrogen peroxide (H 2 O 2 ) encounters the challenges associated with the sluggish kinetics of Fe(II) regeneration. Herein, we developed a carambola-like catalyst of boron (B)-doped TiO 2 mesocrystals-based iron catalyst (Fe-B-MST), which served as a photocatalyst to modulate the regeneration of Fe(II) in photo Fenton-like systems. We successfully used the electrospinning method to gain membrane and realised the remediation of different industrial wastewater. The Fe-B-MST catalyst exhibits excellent efficiencies in the oxidative degradation of 4-chlorophenol (4-CP) pollutants, effectively facilitating the production of • OH while minimising the formation of toxic byproducts, with the first-order kinetic constant ( k = 2.372 min −1 ) being approximately 6.1 times greater than that without B doping, and 19.8 times greater than that observed with commercial TiO 2 . Theoretical calculations and related physicochemical characterisation reveal that B occupies an interstitial site in titania, conferring a sufficiently high valence band potential, making it thermodynamically favourable for H 2 O 2 oxidation and weakening its interaction with • OH, consequently increasing higher reactivity toward the targeted organic pollutant. The B doping facilitates electron transfer, promotes rapid reduction of Fe(III) to Fe(II), and further enhances • OH production via a photo Fenton-like reaction. The oxidation reaction stoichiometry efficiencies were quantified for different organics and calculated to be in the range of 7.70–24.20 % in Fe-B-MST/H 2 O 2 vis. system, representing an enhancement of 1.18–1.54 times compared to Fe-MST/H 2 O 2 vis. , alongside the utilisation efficiency of H 2 O 2 ( η ) of Fe-B-MST/H 2 O 2 vis. is 1.37–1.67 fold greater than that of Fe-MST/H 2 O 2 vis. after 30 min of reaction. This study expands our understanding and provides valuable insights into applying photocatalysis for enhanced wastewater treatment.
研究领域:
环境科学
·
材料科学
✓ 已验证
产品关联
DOI
高影响因子
iScience
·
2021
·
IF 5.458
Yanfei Zeng,Xinyi Zhang,Xianxing Mao,Pei Kang Shen,Douglas R MacFarlane
The Ni-Fe battery is a promising alternative to lithium ion batteries due to its long life, high reliability, and eco-friendly characteristics. However, passivation and self-discharge of the iron anode are the two main issues. Here, we demonstrate that controlling the valence state of the iron and coupling with carbon can solve these problems. We develop a mesostructured carbon/Fe/FeO/Fe 3 O 4 hybrid by a one-step solid-state reaction. Experimental evidence reveals that the optimized system with three valence states of iron facilitates the redox kinetics, while the carbon layers can effectively enhance the charge transfer and suppress self-discharge. The hybrid anode exhibits high specific capacity of 604 mAh⋅g -1 at 1 A⋅g -1 and high cyclic stability. A Ni-Fe button battery is fabricated using the hybrid anode exhibits specific device energy of 127 Wh⋅kg -1 at a power density of 0.58 kW⋅kg -1 and maintains good capacity retention (90%) and coulombic efficiency (98.5%).
研究领域:
材料科学
·
电化学
·
能源存储
✓ 已验证
DOI
PubMed
高影响因子
危险品化学品经营许可证（带存储）