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JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY · 2022 · IF 6.76

Dual-inhibitor composite BTA/PPy/MIL-88(Fe) for active anticorrosion of epoxy resin coatings

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.

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SEPARATION AND PURIFICATION TECHNOLOGY · 2023 · IF 8.6

Photo-Fenton enhanced degradation of antibiotic by Fe single-atom material: Mechanism, performance and adaptability

Qinqin Yu,Youzhi Dai,Zhu Zhang,Bo Feng

A novel photo-Fenton coupling system was constructed in this paper to address the problems of low visible light utilization, narrow pH applicability range and difficult separation and recovery of common photo-Fenton. Fe single-atom material with high activity was used as a bridge connecting photocatalysis and Fenton oxidation, and the performance and mechanism of the coupling system were investigated using a typical antibiotic ciprofloxacin (CIP) as the target pollutant. It was found that the degradation performance of the photo-Fenton coupling system is significantly improved, and can be maintained in acidic, neutral and alkaline wastewaters; the main active species of the coupling system are ·O 2 – , 1 O 2 and h + , and the enhancement mechanism is a combination of Fe single atoms, S-scheme heterojunction and multiple active species.

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SCIENCE OF THE TOTAL ENVIRONMENT · 2023 · IF 9.8

Coupling Fe-Co atomic pair to promote the selective reduction of nitroaromatics under mild conditions

Li Gong,Leben Qiu,Xiaoqian Xing,Jieyun Zhu,Mengzhi Lu,Feier Dong,Yan Yu,Weiting Yu

Selectively reducing nitroaromatics into aromatic amines will not only remove nitroaromatic pollutants in waste effluents to reduce environmental risks, but also yield important feedstocks for chemical industrial manufactures. In this study, a FeCo-co-embedded N-doped Carbon (FeCo-N-C) catalyst with Fe-Co atomic pair has been identified with favorable activity, superior selectivity , excellent reusability, as well as outstanding performance in the treatment of real water. The combined results from theoretical study and experimental tests indicate that the improved catalytic performance of FeCo-N-C is owing to the narrowed band gap and electron delocalization caused by the Fe-Co atomic pair which can improve electron transport in its catalytic reaction. The results of isotope experiments and H* quenching experiments confirm that H 2 O is the source of hydrogen in catalytic reduction of PNP. FeCo-N-C is identified as a superior catalyst to replace multitudinous currently used noble-metal catalysts for the selective catalytic reduction of nitroaromatics in wastewater treatment .

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Results in Physics · 2023 · IF 5.3

Raman study of the spin–lattice excitations of the layered antiferromagnets MPSe3 (M = Fe, Mn)

Jin Qiu,Wen-Juan Huang,Young Jin Lee,Seung Kim,Xiang-Bai Chen,In-Sang Yang

Magnetism in van der Waals (vdW) materials has recently garnered significant attention due to their potential for advanced applications. In this study, we investigate the magnetic transition in layered MPSe 3 (M = Fe, Mn) bulk flakes utilizing temperature-dependent Raman spectroscopy. Our findings reveal unique features in the Raman spectrum that are strongly correlated with the antiferromagnetic ordering in MPSe 3 . We analyze the spin-dependent Raman scattering modes in MPSe 3 by applying the Suzuki–Kamimura formalism. Consequently, our comparative analyses of the spin correlation function and the reduced magnetization provide compelling evidence of the 2D Ising characteristic especially in FePSe 3 . Our results clearly show the potential of MPSe 3 as a prominent platform for exploring fundamental aspects of low-dimensional magnetism.

CAS / MDL: 7439-89-6 7439-96-5
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APPLIED SURFACE SCIENCE · 2023 · IF 6.7

Synergistic effects of Fe-Se dual single-atom sites for boosting electrochemical nonenzymatic H2O2 sensing

Chengcheng Qi,Yuhua Luo,Yongping Dong

The study of single atoms in the field of electrochemical sensing is at the early stage. How to boost the catalytic performance of single atoms is still a big challenge. Herein, we prepare Fe-Se dual single-atom sites on N-doped ultrathin carbon carrier (Fe 1 Se 1 /NC) for realizing highly sensitive nonenzymatic detection of H 2 O 2 . Fe 1 Se 1 /NC was synthesized through the pyrolysis strategy, and then was characterized by transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDS) mapping, high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM), X-ray diffraction (XRD), X-ray photoelectron spectrometer (XPS), and electrochemical techniques, respectively. The results displayed that Fe and Se both existed in an atomically dispersed status. Compared to the single-atom Se or Fe catalyst (Se 1 /NC or Fe 1 /NC), the Fe 1 Se 1 /NC significantly boosted the electrocatalytic activity for H 2 O 2 reduction. The Fe 1 Se 1 /NC modified electrode could be used to detect H 2 O 2 in a wide linear range of 0.02 mM to 13 mM with a high sensitivity of 1508.6 µA·mM −1 ·cm −2 and a low detection limit of 11.5 µM. Moreover, the sensor was successfully employed for detecting H 2 O 2 in disinfectant and urine samples. This work provides a novel design of dual-atom catalysts for excellent electrochemical sensing applications.

CAS / MDL: 56-41-7 108-78-1 69-93-2
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Journal of Environmental Chemical Engineering · 2023 · IF 7.7

Citric acid enhanced oxytetracycline degradation by Fe(Ⅲ)/peracetic acid: Performance, mechanism and influence factors

Yiqing Liu,Lin Tian,Zhenran Wang,Yongsheng Fu,Dandan Zhao

Citric acid (CA) can effectively complex with Fe(Ⅲ) to improve the solubility of Fe(Ⅲ) and accelerate the reduction of Fe(Ⅲ) to Fe(II), while its use in Fe(Ⅲ)-activated peracetic acid (PAA) system has not been reported so far. Therefore, CA was introduced into Fe(Ⅲ)/PAA system in this study to degrade oxytetracycline (OTC), and the degradation efficiency and mechanism of OTC in this system were systematically investigated. The results showed that the removal efficiency of OTC in Fe(Ⅲ)-CA/PAA system at pH 7.0 could reach 81.5% after 20 min, and the degradation of OTC followed pseudo-first-order kinetic. The addition of CA into Fe(Ⅲ)/PAA system could effectively reduce Fe(Ⅲ) to Fe(Ⅱ) driving the cycle of Fe(Ⅲ)/Fe(Ⅱ) and accordingly enhance the OTC removal in this system. According to the results of electron paramagnetic resonance (EPR) and scavenging experiments, hydroxyl radical (HO • ) and organic radicals (CH 3 C(O)O • and CH 3 C(O)OO • ) played major roles for the degradation of OTC in Fe(Ⅲ)-CA/PAA system. Four possible transformation paths of OTC in this system were proposed, including demethylation, hydroxylation, dehydrogenation and dehydration, based on five detected degradation products . This study provides an idea to improve PAA activation by Fe(Ⅲ) and broadens the practical application of Fe(Ⅲ) in advanced oxidation processes .

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CATALYSIS COMMUNICATIONS · 2023 · IF 3.7

Interzeolite conversion synthesized [Fe, Al]-FER zeolites with enhanced hydrothermal stability for NH3-SCR reaction

Li Guo,Jialing Chen,Shaokang He,Tingyu Liang,Lijun Lu,Shenke Zheng,Xinyue Hu,Lan Yi,Xiaoqin Wu

The [Fe, Al]-FER zeolites, which are prepared from the interzeolite conversion method (from MWW to FER topology) with high Al and Fe content (Si/Al of 8–18 and Si/Fe of 11–13), exhibit excellent catalytic performances and hydrothermal tolerance for NH 3 -SCR reaction. The interzeolite conversion process can be tuned by optimizing the zeolite synthesis conditions such as synthesis gel composition, crystallization time, crystallization temperature, and adding MWW seeds. The work can provide a new strategy to synthesize high Al and Fe content zeolite with high hydrothermal stability for NO x removal.

CAS / MDL: 111-49-9
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CHEMOSPHERE · 2022 · IF 8.943

Impacts of anions on activated persulfate oxidation of Fe(II) - Rich potassium doped magnetic biochar

Jiayi Luo,Yunqiang Yi,Long Zhou,Zhanqiang Fang

The potassium-doped magnetic biochar (KMBC) preparation was inevitably introduced the different anions in the process of modifying magnetic biochar (MBC) with different potassium salts, but the effect and mechanism of different anion on KMBC activation properties has not been reported. Therefore, in this paper, five different KMBCs were prepared using several common potassium salts under the same dosage of K + and Fe 2+ , and then was added in the presence of persulfate (PS) for the removal of metronidazole (MNZ). The removal rate of metronidazole was ordered as KMBC K2SO4 (98.40%) > KMBC KNO3 (76.84%) > KMBC KCl (20.79%) > KMBC K2CO3 (19.02%) > KMBC K2C2O4 (14.23%). However, the semi-quantitative of Fe(II) experiments results confirmed that the effectively increase of Fe(II) content by potassium salts modification played the dominant role in improvement of KMBC activation performance. The Fe(II) content of KMBC were ordered as KMBC K2CO3  > KMBC K2SO4  > KMBC KNO3  > KMBC KCl  > KMBC K2C2O4 , with the Fe(II) content of KMBC of 36.74, 17.70, 8.79, 5.24 and 4.85 mg/g, respectively. The indicated that the introduction of different anions would lead to different optimal Fe(Ⅱ) content in KMBC modified with different potassium salts, which was most directly reflected in 1 O 2 content in different KMBC/PS systems, and account for the difference in MNZ degradation efficiency. Meanwhile, when the Fe(II) content in KMBC reached the range of 13.7–28.8 mg/g, KMBC had the better performance of activating PS.

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WATER RESEARCH · 2022 · IF 13.4

Enhanced coagulation and oxidation by the Mn(VII)-Fe(III)/peroxymonosulfate process: Performance and mechanisms

Zheng-Yu Dong,Yi-Li Lin,Tian-Yang Zhang,Chen-Yan Hu,Yang Pan,Renjie Pan,Yu-Lin Tang,Bin Xu,Nai-Yun Gao

To improve the performance of the conventional coagulation process, a permanganate (Mn(VII)) pre-oxidation combined with Fe(III)/peroxymonosulfate (PMS) coagulation process (Mn(VII)-Fe(III)/PMS) that can significantly improve the removal of dissolved organic carbon (DOC), turbidity, and micropollutants is proposed in this study. Compared with conventional Fe(III) coagulation, the Mn(VII)-Fe(III)/PMS process can also significantly enhance the removal of iohexol and sulfamethoxazole in raw water. During this process, the primary reduction product, Mn(IV), after Mn(VII) pre-oxidation was adsorbed on the floc surfaces and involved in the Fe(III)/PMS process. The natural organic matter (NOM) in raw water mediated the redox cycle of iron. The synergistic effect of NOM, Fe, and Mn facilitated the redox cycle of Mn(III)/Mn(IV) and Fe(III)/Fe(II) to promote the activation of PMS. The sulfate radical (SO 4 •− ) played an important role in the degradation of micropollutants. The formation potential of the detected volatile disinfection by-product (DBP) during the subsequent chlorination was reduced by 21.9% after the Mn(VII)-Fe(III)/PMS process. This study demonstrated the promising application of the Mn(VII)-Fe(III)/PMS process for coagulation and micropollutant control and illustrated the reaction mechanism. This study provides guidance for improving conventional drinking water treatment processes.

CAS / MDL: 7647-14-5 7705-08-0
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COMPOSITES PART B-ENGINEERING · 2022 · IF 11.322

Synergistic reinforcement effect of Fe and in-situ synthesized MgAlB4 whiskers in Al matrix composites

Fucheng Wang,Jinfeng Zhang,Kaixin Sun,Liwei Quan,Jing Wang,Naiqin Zhao,Chunsheng Shi,Shijian Zheng

Interfacial bonding is an important factor affecting the mechanical properties of composites. The interface between the in-situ synthesized ceramic phase and the metal matrix is considered ideal, so little attention is paid to the interfacial modification. In this work, we found that interfacial segregation affects the growth of the MgAlB 4 whisker and the interface of reinforcement and matrix in the composites. Systematic experiments and theoretical calculations indicate Fe solute prefer to segregate at the MgAlB 4 - { 10 1 ‾ 0 } /Al interfaces in in-situ synthesized MgAlB 4 /Al composites, which is helpful to reduce system free energy. On the one hand, Fe segregation induces the whisker coarsening and the formation of planar defects with a sandwich structure formed by a layer of Fe atoms and two layers of Al atoms in coarse-whiskers, on the other hand, it improves the interfacial strength . Although extra Fe aggravates the whisker coarsening, the synergistic reinforcing effect of the whiskers and the extra Fe is greater than the sum of their individual reinforcing effects. This work demonstrates that interfacial segregation can be used to modulate the size of reinforcements and improve interfacial strength.

CAS / MDL: 7440-42-8 7439-89-6
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2022 · IF 7.139

Enhancing oxygen reduction reaction performance in acidic media via bimetal Fe and Cr synergistic effects

Nan Xue,Yue Zhang,Chunyan Wang,Xueyan Xue,Dandan Ouyang,Hui Zhu,Jiao Yin

Currently, it is a great challenge to improve the stability of Fe-based oxygen reduction reaction (ORR) catalysts in acidic medium, because the Fenton reaction between Fe-based catalyst and H 2 O 2 will reduce the stability of the catalyst. In this study, Fe, Cr and nitrogen-doped carbon (FeCr-N-C) was synthesized via co-impregnation of biomass walnut shells with metal precursor solutions. The FeCr-N-C catalyst has an onset potential of 0.88 V vs. RHE and outperforms the Fe-N-C catalyst in acidic media. Moreover, FeCr-N-C shows negligible activity decay (ΔE 1/2 = 14 mV) in 0.1 M HClO 4 after 20 000 cycles. The experimental results proved that the bimetal synergism can produce low yield of H 2 O 2 (<2%), which might attribute to variations of local electronic structure. The reactive oxygen species of the catalyst were analyzed by Ultraviolet-visible (UV-Vis) absorption spectra . It was proved that the presence of bimetal inhibited the Fenton reaction between Fe 2+ /Fe 3+ and H 2 O 2 , and further improved the stability of the catalysts. Hence, this study proposes an efficient strategy to facilitate the practical application of Fe-based catalysts in acidic media.

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Journal of Materials Chemistry C · 2022 ·Vol. 10 ·期 46 ·17472-17480 · IF 8.067

TA–Fe(III) complex coated PS nanospheres for non-iridescent structural coloration of cotton fabric

Xiaowei Zhu,Yijiang Li,Tianchen Wei,Yichen Li,Tieling Xing,Matthew D. Shawkey,Guoqiang Chen

Photonic structures constructed from colloidal nanospheres present an attractive prospect for structural coloration in an ecological manner. However, the application of structural color in the field of textile coloration is usually blocked by their uncorrelated scattered light and feeble mechanical properties. Here, a non-iridescent structural color coating with high color saturation and mechanical stability is developed by assembling PS@TA–Fe(III) core–shell nanospheres. The rough surface and low surface charge are favorable for forming amorphous colloid arrays (ACAs) by restricting the crystalline alignment during the assembly process, resulting in non-iridescent structural colors. In addition, the as-prepared structurally colored cotton fabric possesses high color saturation and mechanical stability thanks to the intense light absorption and interface adhesion of the TA–Fe(III) shell. The preparation approach of this structural color coating is facile, low-cost, and environment-friendly, showing promising applications in textile coloration and smart displays.

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