JOURNAL OF ALLOYS AND COMPOUNDS
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2023
·
IF 6.2
Zhitong Xu,Ye Qi,Yueguang Fang,Peng Tian,Guiling Ning,Junwei Ye
Core-shell Fe 3 O 4 @UiO-66-NH 2 nanospheres with superior photocatalytic activity and photo-Fenton performance were synthesized using a layer-by-layer growth strategy. The synthesis involved the use of FeCl 3 , trisodium citrate, sodium acetate, ZrCl 4 , and 2-aminoterephthalic acid as raw materials, with mercaptoacetic acid serving as a modifier. Fe 3 O 4 @UiO-66-NH 2 demonstrated improved visible-light-driven photocatalytic performance in the oxidation degradation of Rhodamine B (RhB) in the presence of trace amounts of H 2 O 2 under visible light irradiation. The Fe(II)/Fe(III) cycle was accelerated by the transfer of the photogenerated electrons (e-) from UiO-66-NH 2 to Fe 3 O 4 , which in turn encouraged the Fenton reaction to produce hydroxyl radicals (•OH). With only 10 mmol/L H 2 O 2 , the removal rate of RhB approached 94% in 120 min. Furthermore, when exposed to visible light, Fe 3 O 4 @UiO-66-NH 2 exhibited 99% efficacious antibacterial activity against Escherichia coli and Staphylococcus aureus . Overall, the as-prepared Fe 3 O 4 @UiO-66-NH 2 core-shell nanospheres show promise for practical applications as photocatalysts for the degradation of organic pollutants and the inactivation of bacteria in wastewater.
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高影响因子
JOURNAL OF MATERIALS SCIENCE
·
2023
·Vol. 58
·期 31
·12596-12610
·
IF 4.5
Liu Jun,Wang Hui,Chang Meng-Jie,Li Wen-Juan,Bai Ge,Xie Heng-Xue,Li Xin,Du Hui-Ling,Song Shi-Jie
MIL-100(Fe) has been demonstrated as a commonly used photocatalyst but is limited by the deficient charge separation efficiency and difficult recovery. In this work, by taking advantages of the strong plasmonic absorption and electron conductivity of Ag nanoparticles, as well as the fast magnetic response of the Fe 3 O 4 , core/shell Ag/Fe 3 O 4 @MIL-100(Fe) (AFM) was facilely prepared by a direct hydrothermal reaction between H 3 btc and Ag/Fe 3 O 4 (AF) for photo-Fenton degradation of RhB assisted by H 2 O 2 . Specifically, the Fe 3 O 4 in AF acted as both ion precursor and protector to inhibit Ag aggregation to obtain uniform and dispersed core/shell AFM. By adjusting the MIL-100(Fe) thickness and the Ag proportion, the optimum AFM exhibits superior photo-Fenton activity to decompose 88.5% RhB within 30 min under visible-light irradiation and H 2 O 2 addition, which is much higher than that of AFM in the presence of either light (58.5%) or H 2 O 2 (46.6%) due to the synergistic effects of visible-light absorption by MIL-100(Fe) and ·OH generation from H 2 O 2 . Moreover, the catalyst can be collected conveniently for its strong magnetic responsibility. This work may be beneficial to the development of effective photo-Fenton catalysts. Graphical abstract A novel magnetically recyclable Ag/Fe 3 O 4 @MIL-100(Fe) with special core/shell structure was facilely synthesized by hydrothermal method with superior photo-Fenton activity for dye degradation.
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
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2023
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IF 5.2
Zhenliang Feng,Jufeng Huang,Hui Guo,Xinyue Zhang,Yuzhu Li,Bo Fang,Yan Li,Guang-Ling Song,Jie Liu
To repair the anti-corrosive coatings directly under seawater is an up-and-coming approach, which can effectively prolong the service life of coated steel structures once the coatings suffered from unexpected scratches. Inspired by the design of Band-Aid for the healing of wound, a magnetic “Band-Aid” (MB) combined with oleic acid modified Fe 3 O 4 nanoparticles (OMNPs) was designed to realize the in-situ repair of anti-corrosion coatings under seawater and the experimental results indicated that this coating repair method by MB incorporated with OMNPs modified epoxy binder is satisfying and effective when the addition of OMNPs epoxy binder was more than 1.0 wt%. Furthermore, the penetration of seawater in the vertical direction of the coating can be prevented by MB during the curing process of epoxy binder, the formation of permeation channels parallel to the coating can be blocked with the aid of OMNPs, which mainly based on the magnetic force between the MB and substrate steel, as well as the competitive-wetting and target-driving functions of OMNPs. The current work may provide a feasible approach to repair the organic anti-corrosion coating directly, which coated on the steel structures under seawater.
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ACS Applied Nano Materials
·
2023
·
IF 5.9
Zhenmao Chen,Yijing Ai,Weiqiang Yang,Li Niu,Qingxiang Wang,Feng Gao
The unique discriminating ability of hydroxyapatite (HAP) to single- and double-stranded nucleic acid implies its potential as a biosensing material for nucleic acid analysis. Herein, a novel immobilization- and label-free electrochemical strategy has been developed for miRNA let-7a detection based on the specific adsorption of magnetic Fe3O4@hydroxyapatite (Fe3O4@HAP) to a duplex structure. Typically, the highly efficient homogeneous reaction between probe DNA (pDNA) and target miRNA let-7a produces the nucleic acid duplex, which is specifically adsorbed on the surface of Fe3O4@HAP. Thereafter, the electroactive intercalator Nile blue (NB) is introduced as the label-free signal molecule and inserts between the stacked base pairs of the pDNA–miRNA duplex. Thus, the Fe3O4@HAP bearing pDNA–miRNA and numerous intercalated NBs are adsorbed by the magnetic glassy carbon electrode, giving rise to an intense sensing signal without the need of nuclease-assisted cyclic amplification. With this advantage, the sensing system shows a wide linear range from 1.0 fM to 100 nM and a low detection limit of 0.051 fM for miRNA let-7a analysis. What is more, the synergy of the base-pairing-driven hybridization, the specific intercalation of NB to the duplex structure, and the selective adsorption of Fe3O4@HAP contribute to a high sensing specificity of the biosensing strategy. The sensing method provides a state-of-the-art strategy for the sensitive and facile bioanalysis and clinical diagnosis of miRNA.
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Journal of Inorganic and Organometallic Polymers and Materials
·
2023
·Vol. 33
·期 8
·2562-2573
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IF 4
Jiang Wenjie,Xu Qianrui,Bu Fengjie,Wei Yingying,Wang Yang,Wang Zhifei,Jiang Yong
In recent decades, magnetic nanomaterials with fast separation and recyclable performance have raised great interest for broad applications in catalysis, protein separation and immunodiagnostics. In this paper, Fe 3 O 4 nanoparticles with a size of (350 ± 50) nm were produced by the solvothermal method. Then, the nanoparticles were coated with a shell made of 3-aminophenol-formaldehyde (APF) resin to prevent agglomeration. The reaction was very rapid, and core–shell Fe 3 O 4 @APF nanospheres were produced by polycondensation within 10 min. Besides, the thickness of the APF shell could be easily adjusted in the range of 10–200 nm by controlling the reaction time and the concentration of 3-aminophenol and formaldehyde. In particular, the APF layer could also act as an effective carrier and reducing agent to capture hundreds of well-dispersed Ag nanoparticles for the abundant hydroxyl groups, obtaining sesame-ball-like Fe 3 O 4 @APF@Ag nanocomposites. The structure of sesame-ball can prevent silver nanoparticles from agglomerating, and Fe 3 O 4 core could provide strong magnetism. The magnetic Fe 3 O 4 @APF@Ag nanomaterials could catalyze the reduction of organic dyes (4-NP, MB and RhB), and the catalyst possessed high activity, with the conversion of dyes remaining above 90% within 3 min after 7 cycles.
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CERAMICS INTERNATIONAL
·
2023
·
IF 5.2
Zeyu You,Ling Weng,Lizhu Guan,Xiaorui Zhang,Zijian Wu
As an excellent two-dimensional insulating material with high thermal conductivity , high temperature stability and high hardness, hexagonal boron nitride(h-BN) is widely applied in semiconductor manufacturing, aerospace, metallurgical manufacturing and other cutting-edge fields. However, the unique surface structure of h-BN leads to poor lubricity and easy agglomeration, which limits the application of h-BN especially in the field of electronic packaging. To address key issues boosted above, this study designed and prepared the BN@Fe 3 O 4 magnetic insulating particles and doped it into the reduced viscosity epoxy resin to prepare the composites. By selecting appropriate external magnetic field strength and BN@Fe 3 O 4 particles’ content, a novel 3D structure of fillers like dominoes in epoxy resin composite was successfully constructed. The microstructure of the BN@Fe 3 O 4 particles and composites were analyzed, the thermal conductivity, the mechanical and the electrical properties of composites were simultaneously tested. Results manifested that the core-shell structures with BN as core and Fe 3 O 4 as shell was successfully prepared, linking through the PDA middle layer between the BN core and Fe 3 O 4 shell. Under the influence of magnetic orientation, the BN@Fe 3 O 4 magnetic particles were preferred an out-of-plane oriented in the epoxy resin composites, resulted an enormously enhanced on thermal conductivity of composites. At a magnetic field strength of 60 mT and 25 vol% BN@Fe 3 O 4 content, the thermal conductivity of BN@Fe 3 O 4 /EP composites is as lofty as 1.832 W/(m K), which is 1023.46% higher than that of pure epoxy resin. Meanwhile, the thermal stability has also been slightly improved, the elastic modulus and insulation performances remain at the same level.
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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
·
2023
·Vol. 30
·期 21
·60574-60589
·
IF 5.8
Zhang Xiaoting,Liu Yang,Qu Lingbo,Han Runping
In this study, a green adsorbent (Fe 3 O 4 -UiO-66-NH 2 ) with the ability of addressing the issues of separation and recovery of UiO-66-NH 2 is obtained using a simple co-precipitation method under environmentally benign conditions. Various characterization techniques are utilized for evaluating the properties of the developed adsorbent. The capability of Fe 3 O 4 -UiO-66-NH 2 towards 2,4-dichlorophenoxyacetic acid (2,4-D) and glyphosate (GP) from solution is explored. The results revealed that the magnetization process did not destroy the crystal structure of UiO-66-NH 2 , which ensured that Fe 3 O 4 -UiO-66-NH 2 had good adsorption performance for 2,4-D and GP. The adsorption processes showed a wide pH application range, high salt tolerance, and regeneration performance as well as an excellent adsorption rate. Results from thermodynamic study showed that both processes were spontaneous and endothermic. The unit uptake ability of Fe 3 O 4 -UiO-66-NH 2 for 2,4-D and GP reached up to 249 mg·g −1 and 183 mg·g −1 from Langmuir model at 303 K, respectively. When solid–liquid ratio was 2 g·L −1 , Fe 3 O 4 -UiO-66-NH 2 can reduce the content of 2,4-D or GP with the initial density of 100 mg·L −1 below the drinking water requirement limit. In addition, the reusability efficiency of Fe 3 O 4 -UiO-66-NH 2 towards 2,4-D and GP was found to be 86% and 80% using 5 mmol·L −1 NaOH as eluent. Analysis of simulated water samples indicated that Fe 3 O 4 -UiO-66-NH 2 could achieve the single or simultaneous removal of 2,4-D and GP from wastewater. Summarily, Fe 3 O 4 -UiO-66-NH 2 as a green adsorbent can serve as an alternative for removing 2,4-D and GP from water body.
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高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2023
·
IF 15.1
Siqi Tong,Dan Chen,Xinbai Jiang,Zhixiang Xu,Xiaodong Liu,Jinyou Shen
A novel composite biochar synthesized from Fenton sludge (FS) and sewage sludge (SS) was employed to catalyze persulfate for the removal of 1-H-1,2,4-triazole (TZ). The optimized conditions for the synthesis and operating process were identified through response surface methodology as follow: SS/FS mass ratio = 5:1, catalyst dosage = 0.9 g L −1 and PDS concentration = 0.5 g L −1 . The removal efficiencies of TZ, TOC and organic nitrogen were found to be as high as 97.6%, 80.33% and 100%, respectively, with the addition of Fe 3 O 4 -doped biochar in persulfate catalytic system. Besides, Fe 3 O 4 -doped biochar exhibited superior stability and tolerance to wide range of pH (2–12), temperature (15–45 °C) and co-existing substrate. The reactive oxygen species, which resulted in the catalytic degradation of TZ followed the order of SO 4 ∙− > ∙OH > O 2 ∙− > 1 O 2 , were identified by electron spin resonance and quenching tests. It demonstrated that the radical pathway accomplished with non-radical pathway contributed to the enhanced degradation of TZ, which was further identified by electrochemical experiments. Moreover, the possible degradation pathway of TZ was ascertained and proposed through DFT calculation and LC-MS analysis. These findings illustrated that the novel magnetic biochar would be a promising persulfate catalyst for the treatment of refractory organic matters. In addition, it also provided a new alternative method for the resource utilization of FS and SS.
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ADVANCED POWDER TECHNOLOGY
·
2023
·
IF 5.2
Tingting Mao,Qihui Ding,Qian Shan,Xiaochen Chang,Wei Wu
In this paper, a magnetic ferrosoferric oxide/two-dimensional molybdenum disulfide (Fe 3 O 4 /2D-MoS 2 ) composite material was successfully prepared by combining liquid phase exfoliation and in-situ liquid phase co-precipitation methods with scalable and facile characteristics and applied to catalyze the degradation of tetracycline (TC) during the peroxymonosulfate-based advanced oxidation processes (PMS-AOPs), which is a typical and widely used antibiotic. The morphology and crystallinity of the composites were determined by scanning electron microscopy, transmission electron microscope and X-ray diffraction, respectively. And its BET surface area was tested by N 2 adsorption and desorption curves. For the PMS-AOPs, the effects of iron loading, different systems, initial concentration of pollutants, dosage of the composites, concentration of peroxymonosulfate (PMS) and solution initial pH on the removal of TC were researched in details. The results showed that it could reach 89.0% degradation efficiency within 90 min for 50 mg/L TC with the as-prepared composites as catalyst, showing good catalytic performances. In addition, the mechanisms of the reaction were deduced by quenching experiments and X-ray photoelectron spectroscopy analysis. It was turned out that the as-synthsized material has a broad applying prospect in PMS-AOPs.
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ENVIRONMENTAL RESEARCH
·
2023
·
IF 8.3
Wenjun Zhu,Xiaohua Zuo,Xiaofei Zhang,Xiangyi Deng,Deng Ding,Chunlei Wang,JunTao Yan,Xiaobo Wang,Guanghui Wang
A novel CuO–Fe 3 O 4 encapsulated in the carbon framework with abundant oxygen vacancies (CuO–Fe 3 O 4 @C) was successfully prepared by thermal conversion of Cu(OAc) 2 /Fe-metal organic framework. The as-prepared catalyst exhibited excellent peroxymonosulfate (PMS) activation performance, good recyclability and fast magnetic separation. Under optimal conditions, the added BPA (60 mg/L) could be completely removed by CuO–Fe 3 O 4 @C/PMS system within 15 min with the degradation rate constant ( k ) of 0.32 min −1 , being 10.3 and 246.2 times that in CuO/PMS (0.031min −1 ) and Fe 3 O 4 /PMS (0.0013 min −1 ) system. A deep mineralization rate of BPA (＞80%) was achieved within 60 min. The results demonstrated the synergistic effect of bimetallic clusters, oxygen vacancies and carbon framework was a key benefit for the exposure of more active sites, the electron donor capacity and the mass transfer of substrates, thereby promoting the decomposition of BPA. Capture experiments and EPR indicated that 1 O 2 was the predominant reactive oxygen species (ROSs). The degradation routes of BPA and the activation mechanism of PMS were proposed. This study offers an opportunity to develop promising MOFs-derived hybrid catalysts with tailored structures and properties for the practical application of SR-AOPs.
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高影响因子
JOURNAL OF MATERIALS SCIENCE
·
2023
·Vol. 58
·期 13
·5587-5598
·
IF 4.5
Sun Shanshan,Zhang Zihao,Li Shuhan,Le Jinxun,Qian Haixia,Yin Xiaoshuang,Liu Ying,Yang Wenzhong,Chen Yun
Magnetic core–shell nanomaterial Fe 3 O 4 –SiO 2 –Cu 2 O/Cu was first successfully synthesized using an economical strategy. Using Fe 3 O 4 as a magnetic center for easy recycling and SiO 2 as the connecting layer, Cu elements were evenly and steadily distributed on the surface of the Fe 3 O 4 –SiO 2 –Cu 2 O/Cu core–shell nanostructure. The magnetic catalyst performed outstanding catalytic reduction activity for 4-nitrophenol (4-NP), and the complete catalytic reduction of 4-NP was achieved within only 5 min. What’s more, the catalyst could be well recycled, and the catalytic efficiency remained more than 90% after being reused 24 times. Graphical abstract
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RSC Advances
·
2019
·Vol. 9
·期 2
·766-780
·
IF 3.049
Lin Guo,Sheng-Shuai Gao,Qing-Da An,Zuo-Yi Xiao,Shang-Ru Zhai,Dong-Jiang Yang,Li Cui
Dopamine-derived cavities/Fe3O4 nanoparticles-encapsulated carbonaceous composites with self-generating three-dimensional (3D) network structure were successfully fabricated by a facile synthetic method, in which sodium alginate provided carbon matrix pores and excellent microwave absorption performance was established. The hollow cavities derived from the core–shell-like CaCO3@polydopamine were creatively introduced into the 3D absorber to significantly improve the absorption performance. The sample calcined at 700 °C exhibited the most outstanding microwave absorption performance, with minimal reflection loss up to −50.80 dB at 17.52 GHz with a rare thickness of only 1.5 mm when filler loading was 35% in paraffin matrix. The effective absorption bandwidth of reflection loss < −10 dB reached 3.52 GHz from 14.48 GHz to 18 GHz, corresponding to the same thickness of 1.5 mm. In contrast, the sample without hollow dopamine-derived cavities showed poor performance due to poor impedance matching, and this highlights the role of hollow cavities brought into the 3D structure, which led to a difference in interfacial polarization, multiple reflections and scattering. The novel dopamine-derived cavities/Fe3O4 nanoparticles-encapsulated carbonaceous composites with 3D network structure can be regarded as a promising candidate for application as a microwave absorber with strong absorption.
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