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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2017 · IF 2.714

Fe/Fe3C nanoparticles loaded on Fe/N-doped graphene as an efficient heterogeneous Fenton catalyst for degradation of organic pollutants

Xiaoqin Huang,Yanli Niu,Weihua Hu

Heterogeneous Fenton catalyst with high activity and excellent durability is highly demanded for efficient removal of organic pollutants via well-known Fenton reaction. In this work Fe/Fe 3 C nanoparticles loaded on iron/nitrogen-doped graphene (Fe/Fe 3 C @ Fe/N-Graphene) were synthesized via spontaneous oxidative polymerization of dopamine (DA) on graphene oxide (GO) surface in the presence of iron (III) chloride, followed by thermal annealing. The Fenton catalytic performance of as-prepared Fe/Fe 3 C @ Fe/N-Graphene was evaluated by degrading rhodamine 6G (Rh 6G) as a model organic pollutant. It is found that as-prepared catalyst demonstrates good activity with a rate constant of 0.080   min −1 under optimal hydrogen peroxide (H 2 O 2 ) concentration and catalyst dosage. Moreover, its catalytic activity shows negligible decrease even after 13 successive cycles, exhibiting excellent catalytic durability. The possible mechanism behind the improved Fenton catalytic activity and durability was further discussed.

CAS / MDL: 7782-42-5
研究领域: 环境科学 · 材料科学
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CARBON · 2019 · IF 7.466

Fe-doped LiMnPO4@C nanofibers with high Li-ion diffusion coefficient

Hao Yang,Cuimei Fu,Yijian Sun,Lina Wang,Tianxi Liu

Olivine-type LiMnPO 4 (LMP) cathodes have gained enormous attraction for Li-ion batteries (LIBs) due to high discharge platform, theoretical capacity and thermal stability. However, it is still challenging to achieve encouraging Li-storage behavior owing to the low electronic conductivity and slow Li-ion diffusion rate of LMP. Here, the electrochemical behavior of fibrous LiFe x Mn 1-x PO 4 @carbon (LF x M 1-x P@C, x = 0, 0.25, 0.5, 0.75, 1) composites with different Fe doping amounts is investigated. Among the composites, LF 0.5 M 0.5 P@C demonstrates a superior cell performance due to a higher Li-ion diffusion coefficient (D Li ), resulting from a proper Fe doping ratio and a more uniform morphology. At a current rate of 0.2 C (1 C = 170 mA g −1 ), the LF 0.5 M 0.5 P@C cathode delivers a specific capacity of 150 mAh g −1 up to 500 cycles with a capacity retention of 119%. A longer-term cycling at 5 C for 2000 cycles can be maintained with a reversible capacity exceeding 102 mAh g −1 . The fundamental study provides an insightful guidance for future design of cathode materials with high performance.

研究领域: 材料科学 · 电化学
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JOURNAL OF SOLID STATE CHEMISTRY · 2021 · IF 3.498

Fe-doped LaNi1-xFexO3 perovskite oxides for enhanced visible-light-driven photocatalytic activity

Li Zeng,Tongjiang Peng,Hongjuan Sun,Jingjie Yang,Yao Li,Yating Qin

A series of Fe-doped LaNi 1-x Fe x O 3 perovskite oxide photocatalytic materials was prepared using a sol-gel method. The phase composition and morphology of LaNi 1-x Fe x O 3 samples were characterized via X-ray diffraction, scanning electron microscopy, transmission electron microscopy , X-ray photoelectron spectroscopy, and other analytical methods. The photocatalytic performance of the samples was tested by assessing the degradation rate of methyl orange. According to the results, Fe-doping caused the lattice distortion of the initially cubic of LaNiO 3 to a rhombohedral crystal system . In turn, partial substitution of Ni with Fe was found to increase the amount of oxygen vacancies , resulting in the higher mobility of lattice oxygen and thus improving the photocatalytic activity . The best photocatalytic performance was found in a LaNi 0.95 Fe 0.05 O 3 sample with a 5% Fe dopant concentration. Furthermore, the degradation rate of methyl orange in LaNi 0.95 Fe 0.05 O 3 within 120 ​min of visible light irradiation was as high as 98.89%, and its good degradation effect even with respect to other organic dyes such as methylene blue and rhodamine B. Finally, LaNi 0.95 Fe 0.05 O 3 was shown to maintain high photocatalytic activity and excellent recyclability even after numerous operation cycles.

研究领域: 材料科学 · 环境科学
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JOURNAL OF CATALYSIS · 2017 · IF 6.844

Sn promoted BaFeO3−δ catalysts for N2O decomposition: Optimization of Fe active centers

Chuande Huang,Yanyan Zhu,Xiaodong Wang,Xin Liu,Junhu Wang,Tao Zhang

A series of BaFe 1− x Sn x O 3− δ catalysts were prepared by sol-gel method and tested for N 2 O decomposition to shed light on the effect of B-site substitution on the catalytic behavior of perovskite catalysts. 119 Sn and 57 Fe Mössbauer results confirmed that the 5-fold coordinated Fe 3+ cations with one adjacent oxygen vacancy (Fe 3+ O 5 ) were the main active centers for N 2 O decomposition. Doping of Sn cations can significantly improve the percentage of Fe 3+ O 5 from 30% ( x   =   0) to 68% ( x   =   0.8). More importantly, the valence state of Fe could be gradually reduced due to weakening of Fe O bond with increasing the Sn content, which was attributed to the stronger force of Sn than Fe in Fe O Sn structure to draw the oxygen anion and expansion of unit cell volume. Such change of Fe chemical state favored the oxygen mobility of the catalyst, leading to reduction in activation energy for N 2 O decomposition from ca. 241 ( x   =   0) to 178   kJ   mol −1 ( x   =   0.8). BaFe 0.2 Sn 0.8 O 3− δ catalyst exhibited the highest intrinsic rate of 1.49   s −1 (550   °C), nearly 4 times larger than that of BaFeO 3− δ (0.43   s −1 ).

CAS / MDL: 7782-61-8 814-94-8
研究领域: 催化化学 · 材料科学
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ELECTROCHIMICA ACTA · 2024 · IF 5.5

Carbon nanotubes cross-linked Fe/Fe3C nanoparticles and Fe single atoms as high-efficiency bifunctional oxygen electrocatalyst for rechargeable zinc-air batteries

Zhiwen Xu,Lanlu Lu,Weiwei Chen,Fei Yang,Guimei Liu,Yan Sun,Xiaoyi Qiu,M. Danny Gu,Ping Gao,Dong Su,Minhua Shao

Although zinc-air batteries (ZABs) have made great progress in recent years, there still a great challenge to develop low-cost bifunctional electrocatalysts with high catalytic activity and stability. Herein, we report a bifunctional oxygen electrocatalyst consisting of ZIF-derived carbon-anchored Fe/Fe 3 C nanoparticles and Fe single atoms, which are crosslinked by carbon nanotubes (denoted as CNT@Fe/Fe 3 C||FeNC). Benefiting from the synergetic effect of Fe/Fe 3 C nanoparticles, Fe-N 4 active sites, and the 3D interpenetrating network structure, CNT@Fe/Fe 3 C||FeNC shows excellent bifunctional catalytic activities with a low ΔE of 0.671 V. Furthermore, the assembled rechargeable ZAB demonstrates a high peak power density of 187 mW cm –2 and shows excellent cycling stability up to 600 h This work provides new ideas for constructing non-precious metal bifunctional catalysts for practical applications in ZABs.

CAS / MDL: 693-98-1 10196-18-6
研究领域: 材料科学 · 电化学 · 能源存储与转换
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Materials Science and Engineering B-Advanced Functional Solid-State Materials · 2024 · IF 3.9

Efficient removal of arsenic from wastewater using aminated Fe-BTC-based Metal-Organic frameworks

Boyu Du,Nan Jiang,Zengbin Chai,Chao Liu,Xing Zhu

DETA-Fe-BTC MOFs with an irregular porous structure is fabricated by a hydrothermal method combining with Diethylenetriamine (DETA) modification and investigated in batch adsorption experiments for arsenic removal from wastewater. DETA-Fe-BTC show high adsorption ability in wide pHs ranged from 2 to 12 and a wide arsenic concentration range from 1 mg/L to 1000 mg/L. The maximal arsenic adsorption capacity reaches 1748.50 mg/g at a pH of 10. Besides, the MOFs reveal a super-fast arsenic-removal rate. 90.58 % of arsenic was removed from wastewater with an initial arsenic concentration of 40 mg/L in 5 s. Arsenic adsorption kinetics and isotherms follow a chemical adsorption mode and a single-molecule adsorption mode that the MOFs offer abundant Fe 3+ active cites forming Fe-O-As coordination with arsenate or arsenite. Considering its strong recyclability and high efficiency, DETA-Fe-BTC will be used as a potential arsenic scavenger for the disposal of arsenic contaminated groundwater or industrial wastewater.

CAS / MDL: 64-17-5 111-40-0 68-12-2
研究领域: 环境科学 · 材料科学
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NEW JOURNAL OF CHEMISTRY · 2024 ·Vol. 48 ·期 20 ·9185-9195 · IF 2.7

Construction of an MIL-101(Fe)/layered bimetallic oxide heterojunction for enhanced ciprofloxacin removal

Shikai Xue,Dongying Zhu,Qing Zuo,Shuangfeng Yang,Haiyan Wang,Qiujun Lu,Guoxing Yin,Guihua Ruan,Fuyou Du

A novel MIL-101(Fe)/ZnCrZr-LBMO heterojunction was successfully constructed and used for the removal of ciprofloxacin (CIP) in this work. The MIL-101(Fe)/ZnCrZr-LBMO composite exhibited significantly enhanced photocatalytic degradation activity, with reaction rates approximately 3.4 and 3.1 times faster than those observed with pristine MIL-101(Fe) and ZnCrZr-LBMO, respectively. The effect of different amounts of ZnCrZr-LBMO, sample pH, CIP concentration, inorganic cations, and anions on CIP removal was investigated, and the possible intermediates and degradation pathways of CIP were speculated. The·O2− radicals dominated CIP degradation, with minor contributions from 1O2, h+, and ·OH radicals. The composite exhibited high removal rates for CIP (94.7%), ofloxacin (86.8%), and tetracycline (96.3%), respectively, within 60 min of light irradiation, and excellent reusability, retaining over 85.1% CIP degradation rate after five cycles. Our work provides a new reference to construct highly efficient and easily recyclable MIL-101(Fe)/ZnCrZr-LBMO photocatalysts for the removal of antibiotic pollutants, promising advancements in real water treatment applications.

研究领域: 环境科学 · 材料科学
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LANGMUIR · 2024 · IF 3.7

Photocatalytic Selective Oxidation of Toluene over Chlorine-Coordinated MIL-101(Fe) under Ambient Conditions

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.

研究领域: 化学 · 材料科学 · 环境科学
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MOLECULES · 2024 ·Vol. 29 ·期 17 ·4194 · IF 4.2

The Role of Fe(III) in Selective Adsorption of Pullulan on Calcite Surfaces: Experimental Investigation and Molecular Dynamics Simulation

Kaiwei Ding,Tingsheng Qiu,Xianhui Qiu,Guanfei Zhao,Qinghao Jiao,Jiangjie Fang,Ruisen Lai,Wenhui Yang

The floatability of fluorite and calcite exhibit similar properties, rendering their flotation separation challenging. Macromolecular polysaccharide reagents containing the polyhydroxyl group have shown broad promising application. The selectivity of polysaccharide is relatively low. In this study, the introduction of Fe3+was employed to enhance the selective adsorption capacity of Pullulan polysaccharide towards fluorite and calcite minerals, thereby achieving effective flotation separation. Furthermore, the mechanism underlying intramolecular interactions was elucidated. The DFT calculation and XPS analysis revealed that the adsorption of Fe3+on the calcite surface was more favorable, leading to the formation of a Ca-O-Fe structure. The MD simulation, XPS analysis, and Zeta potential analysis revealed that the Fe-OH groups on the surface of calcite reacted with the -OH groups in Pullulan and formed bonds, resulting in the formation of a Calcite-Fe-Pullulan structure. This facilitated the attachment of a significant number of Pullulan molecules to the calcite surface. The formation of a hydrophilic layer on the outer surface of calcite by Pullulan, in contrast to the absence of such layer on fluorite’s surface, results in an increased disparity in surface floatability between these two minerals, thereby enhancing the efficiency of flotation separation.

CAS / MDL: 7647-01-0
研究领域: 矿物学 · 表面化学 · 分子动力学模拟
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MICROPOROUS AND MESOPOROUS MATERIALS · 2022 · IF 5.876

Delignified wood supported MIL-100 (Fe) for fast adsorption removal of tetracycline

Xiuying Zhu,Mengjie Li,Xiong-Fei Zhang,Jianfeng Yao

Iron-based metal-organic framework (MIL-100) with intrinsic high surface area and low cost is extremely attractive in the field of organic pollutant remediation. Herein, delignified balsa wood is utilized as substrate/support for the in situ growth and dispersion of MIL-100 particles. Results demonstrate that the MIL-100 particles adhere tightly to the support and a hierarchal architecture is constructed. The MIL-100@Wood composite can be used as adsorbent and filter for the alleviation of organic contamination. With 25.4 wt% of MIL-100 loading, the MIL-100 decorated delignified wood (MD-Wood) exhibits a tetracycline (TC) adsorption capacity of 109.9 mg/g. The composite MD-Wood can be easily fabricated into an all-in-one filter and this filter presents an effective treatable volume of 1100 mL of TC solution (20 mg/L). The MD-Wood is further deposited with Ag particles and the Ag@MD-Wood can be directly applied for the flow catalytic reduction of 4-nitrophenol. Moreover, the composite woods are facile to regenerate and possess superior reusability and stability.

研究领域: 环境科学 · 材料科学
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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH · 2015 ·Vol. 23 ·期 7 ·6758-6766 · IF 2.828

Enhanced degradation of benzene by percarbonate activated with Fe(II)-glutamate complex

Fu Xiaori,Gu Xiaogang,Lu Shuguang,Miao Zhouwei,Xu Minhui,Zhang Xiang,Danish Muhammad,Cui Hang,Farooq Usman,Qiu Zhaofu,Sui Qian

Effective degradation of benzene was achieved in sodium percarbonate (SPC)/Fe(II)-Glu system. The presence of glutamate (Glu) could enhance the regeneration of Fe(III) to Fe(II), which ensures the benzene degradation efficiency at wider pH range and eliminate the influence of HCO 3 − in low concentration. Meanwhile, the significant scavenging effects of high HCO 3 − concentration could also be overcome by increasing the Glu/SPC/Fe(II)/benzene molar ratio. Free radical probe compound tests, free radical scavenger tests, and electron paramagnetic resonance (EPR) analysis were conducted to explore the reaction mechanism for benzene degradation, in which hydroxyl radical (HO•) and superoxide anion radical (O 2 •− ) were confirmed as the predominant species responsible for benzene degradation. In addition, the results obtained in actual groundwater test strongly indicated that SPC/Fe(II)-Glu system is applicable for the remediation of benzene-contaminated groundwater in practice.

研究领域: 环境科学 · 化学工程
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CHEMICAL ENGINEERING JOURNAL · 2019 · IF 8.355

Visible light induced photocatalytic reduction of Cr(VI) by self-assembled and amorphous Fe-2MI

Qiaoyuan Gao,Dagang Lin,Yongjie Fan,Qin He,Qi Wang

Visible-light-active Fe-2MI assemblies were prepared at room temperature using 2-Methylimidazole (2MI) as organic ligand to form complex with Fe(II) or Fe(III). TGA and XRD characterizations indicated that Fe(II) can form more stable complex and higher coordinating percentage with 2MI relative to Fe(III). Besides, Fe(II)-2MI displayed amorphous state with larger BET surface area and higher photocurrent response. At very low catalyst dosage (0.1 g/L), highest activity for Cr(VI) reduction can be achieved using Fe(II)-2MI as photocatalyst. The estimated pseudo-first-order rate constant (0.021 min −1 ) was 1.4 and 2.1 times that on Fe(III)-2MI and Fe(II)-NaOH, respectively. The well-known ZIF-67 (Co-2MI), ZIF-7 (Zn-2MI) and Fe-MOFs with other organic ligands (H 2 BDC, NH 2 -H 2 BDC or FA) were also used as control samples. Optimal activity for photocatalytic reduction of Cr(VI) was achieved by Fe(II)-2MI. The operating factors was optimized at acidic pH (2.0), higher catalyst dosage (0.3 g/L) and appropriate concentration of coexisting organics (2.0 mM) within the tested range. The stability of Fe(II)-2MI was investigated at different pH values (2, 3 and 4.64), which all displayed good stability. Mechanism study indicated that Fe(II)-2MI has adequate conduction and valence band positions for Cr(VI) reduction and organics oxidation, respectively. Therefore, the as-prepared amorphous Fe(II)-2MI assemblies may be cheap, stable and easy available candidate for the photocatalytic disposal of Cr(VI)-containing wastewaters.

研究领域: 环境科学 · 材料科学
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