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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2016 · IF 3.782

Enhanced removal of trace Cr(VI) from neutral and alkaline aqueous solution by FeCo bimetallic nanoparticles

Nannan Qin,Ya Zhang,Hongjian Zhou,Zhigang Geng,Gang Liu,Yunxia Zhang,Huijun Zhao,Guozhong Wang

The reactivity of zero valent iron (Fe 0 ) for removing Cr(VI) is self-inhibiting under neutral and alkaline conditions, due to the precipitation of ferrous hydroxide on the surface of Fe 0 . To overcome this difficulty, we incorporated a second metal (Co) into Fe 0 to form FeCo bimetallic nanoparticles (FeCo BNPs), which can achieve higher activity and significant improvement in the reaction kinetics for the removal of Cr(VI) compared with Fe 0 . The FeCo BNPs were synthesized by a hydrothermal reduction method without using any templates. The characterization analysis indicated that the products were highly uniform in large scale with 120–140   nm size in diameter. The obtained FeCo BNPs exhibited a remarkable removal ability for Cr(VI) in the pH range of 5.3–10.0. Especially, FeCo BNPs were able to reduce trace Cr(VI) (1.0   mg   L −1 , pH   =   7.5) down to about 0.025   mg   L −1 within 1   h. XPS analysis confirmed that Cr(VI) was reduced to Cr(III) by FeCo BNPs, while Fe and Co was oxidized, implying a chemical reduction process. The enhanced removal of trace Cr(VI) could be originated from the introduction of Co, which not only served as a protecting agent against surface corrosion by galvanic cell effect, but also enhanced the efficient flow of electron transfer between iron and Cr(VI). All the results primarily imply that FeCo BNPs can be employed as high efficient material for wastewater treatment.

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JOURNAL OF CHROMATOGRAPHY A · 2017 · IF 3.981

Pyrolytic in situ magnetization of metal-organic framework MIL-100 for magnetic solid-phase extraction

Shu-Hui Huo,Hai-Yan An,Jing Yu,Xue-Feng Mao,Zhe Zhang,Lei Bai,Yan-Feng Huang,Peng-Xin Zhou

In this study, we report a facile, environmental friendly fabrication of a type of magnetic metal-organic framework (MOF) MIL-100 that can be used for magnetic solid-phase extraction (MSPE). The magnetic MOF composites were fabricated using in situ calcination method. The as-synthesized materials exhibited both high porosity and magnetic characteristics. They used for the MSPE of polycyclic aromatic hydrocarbons (PAHs) from water samples. Such MOF-based magnetic solid-phase extraction in combination with gas chromatography equipped with a flame ionization detector (GC-FID), exhibited wide linearity (0.02–250   μ g   L −1 ), low detection limits (4.6-8.9   ng   L −1 ), and high enrichment factors (452–907) for PAHs. The relative standard deviations (RSDs) for intra- and inter-day extractions of PAHs were ranging from 1.7% to 9.8% and 3.8% to 9.2%, respectively. The recoveries for spiked PAHs (1   μ g   L −1 ) in water samples were in the range of 88.5% to 106.6%. The results showed that the special anion-π orbital (electron donor-acceptor) interaction and π-π stacking between magnetic MIL-100 and PAHs play an important role in the adsorption of PAHs.

CAS / MDL: 7439-89-6
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CERAMICS INTERNATIONAL · 2017 · IF 2.986

Preparation and characterization of iron/β-tricalcium phosphate bio-cermets for load-bearing bone substitutes

Fupo He,Guowen Qian,Weiwei Ren,Jinhuan Ke,Peirong Fan,Xuetao Shi,Yanling Cheng,Shanghua Wu,Xin Deng,Jiandong Ye

Ceramic-metal composite materials, namely cermets, are provided with characteristics of both ceramic and metal. Herein, for the first time bio-cermets based on β-tricalcium phosphate (β-TCP) bioceramic with biodegradable iron being reinforcement phase, were fabricated using the powder metallurgic method. The phase composition, microstructure, mechanical properties and in vitro cell behaviors of bio-cermets were investigated. The results revealed that atomic diffusion occurred between the iron and β-TCP matrix during the sintering process. The bio-cermets attained remarkable increase in fracture toughness (1.16–1.55   MPa   m 1/2 ) compared to the β-TCP bioceramic (0.54   MPa   m 1/2 ). The bio-cermets with 10   vol% iron showed the highest compressive strength (640   MPa), significantly higher than that of plain β-TCP bioceramic (285   MPa). The in vitro cell behaviors test indicated that the bio-cermets did not showed any sign of toxicity; the iron ions released from bio-cermets up-regulated bone-related gene expression of bone mesenchymal stem cells. The bio-cermets developed in this study represent potential bone substitutes for application in the load-bearing bone defects.

CAS / MDL: 7439-89-6 8042-47-5
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Journal of Materials Chemistry C · 2016 ·Vol. 4 ·期 32 ·7614-7621 · IF 5.066

Tunable hierarchical Fe nanowires with a facile template-free approach for enhanced microwave absorption performance

Junyao Shen,Yongtao Yao,Yanju Liu,Jinsong Leng

We demonstrate a facile, template-free route for Fe nanowires (NWs) with an average diameter of 100 nm through magnetic-field-assisted hydrothermal conditions. The aspect ratio of the Fe NWs reaches 50. Fe NWs are constructed with interconnected bead-like nanospheres, which are composed of primary nanocrystals (NCs) with an average size of 8 nm. This shows that the polycrystalline Fe NWs have a body-centred cubic (bcc) structure with preferential growth on the 〈110〉 zone axis. Such hierarchical structures involve orientational growth in the presence of an external magnetic field. The molarity of the reducing agent, reaction time and temperature, are further investigated to understand the influence of these parameters on the growth process of Fe NWs. Compared with those of Fe nanoparticles (NPs), the magnetic properties of Fe NWs show both higher saturation magnetization (154.03 emu g−1) and coercivity (360.84 Oe). The peak value of reflection loss (RL) reaches up to −27.28 dB at 3.68 GHz, indicating the excellent microwave absorption performance of the Fe NWs for low gigahertz usage (2–6 GHz). This mild approach to control Fe NWs is easy to scale-up for other iron-related magnetic nanodevice applications.

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JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY · 2016 ·Vol. 92 ·期 3 ·552-561 · IF 2.738

Oxidation of N-nitrosodimethylamine in a heterogeneous nanoscale zero-valent iron/H2O2 Fenton-like system: influencing factors and degradation pathway

Lin Wang,Juan Yang,Yongmei Li,Juan Lv,Gucheng Li

BACKGROUND N-nitrosodimethylamine (NDMA) is an emerging disinfection byproduct, which is also classified as a potential carcinogen and mutagen. Advanced oxidation processes based on hydroxyl radical (•OH) have been suggested as an effective NDMA elimination method. This study focused on investigating the mechanism of oxidative degradation of NDMA using a nanoscale zero-valent iron (nZVI) induced heterogeneous Fenton system. RESULTS The results show that nZVI was stable in the system. NDMA (≤1 mg L −1 ) was completely removed in 60 min under the following optimal conditions: initial pH =3.0, H 2 O 2 concentration =2 mmol L −1 and nZVI dose =56 mg L −1 . Major dissolved species (such as HCO 3 − , Cl − and humic acid) in a natural water matrix reduced the degradation rate of NDMA. During the degradation of NDMA, eight degradation intermediates were detected and confirmed, including methylamine (MA), dimethylamine (DMA), ammonia (AM), nitromethane (NM), hydroxyurea (HU), acetaldehyde (AA), NO 2 − and NO 3 − . Based on the identified intermediates, a tentative degradation pathway of NDMA in the nZVI/H 2 O 2 system was proposed. CONCLUSION Results indicate that nZVI as the catalyst used in the heterogeneous Fenton system is an effective alternative to remove NDMA. © 2016 Society of Chemical Industry

CAS / MDL: 7439-89-6
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CHEMICAL ENGINEERING JOURNAL · 2016 · IF 5.31

Simultaneous removal of bisphenol A and phosphate in zero-valent iron activated persulfate oxidation process

Li Zhao,Yuefei Ji,Deyang Kong,Junhe Lu,Quansuo Zhou,Xiaoming Yin

In this study, the removal of bisphenol A (BPA) and phosphate in zero-valent iron activated persulfate (ZVI/PS) oxidation process was investigated. Activation of PS by ZVI mainly produces strong oxidizing sulfate radicals (SO 4 − ) which can efficiently degrade organic contaminants. ZVI is ultimately transformed to ferric iron (Fe 3+ ) which works as a coagulant to remove phosphate. It was demonstrated that BPA and phosphate could be simultaneously removed in this system. The oxidation of BPA in ZVI/PS process followed pseudo-first-order kinetics. The reaction rate increased with increased PS and ZVI dosage. Eight transformation products were identified using gas chromatography–mass spectrometry (GC–MS) technique. SO 4 − -induced oxidative transformation of BPA included electron transfer and hydrogen abstraction mechanisms. Carbonate exhibited no obvious influence on the removal both of phosphate and BPA. Natural organic matter (NOM) showed inhibitory effect on BPA degradation but had no appreciable negative effect on phosphate removal. Simultaneous removal of BPA and phosphate was also observed in wastewater treatment plant effluent with relatively high efficiency. The results of this work indicate that ZVI/PS process could serve as a novel treatment technique for removal of trance organic contaminants and phosphate simultaneously.

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Nature Communications · 2016 ·Vol. 7 ·期 1 ·1-8 · IF 11.329

Scrutinizing the double superconducting gaps and strong coupling pairing in (Li1−xFex)OHFeSe

Du Zengyi,Yang Xiong,Lin Hai,Fang Delong,Du Guan,Xing Jie,Yang Huan,Zhu Xiyu,Wen Hai-Hu

In the field of iron-based superconductors, one of the frontier studies is about the pairing mechanism. The recently discovered (Li 1− x Fe x )OHFeSe superconductor with the transition temperature of about 40 K provides a good platform to check the origin of double superconducting gaps and high transition temperature in the monolayer FeSe thin film. Here we report a scanning tunnelling spectroscopy study on the (Li 1− x Fe x )OHFeSe single crystals. The tunnelling spectrum mimics that of the monolayer FeSe thin film and shows double gaps at about 14.3 and 8.6 meV. Further analysis based on the quasiparticle interference allows us to rule out the d -wave gap, and for the first time assign the larger (smaller) gap to the outer (inner) Fermi pockets (after folding) associating with the d xy ( d xz /d yz ) orbitals, respectively. The gap ratio amounts to 8.7, which demonstrates the strong coupling mechanism in the present superconducting system.

CAS / MDL: 7439-89-6
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JOURNAL OF HAZARDOUS MATERIALS · 2016 · IF 4.836

Heavy metal removal using nanoscale zero-valent iron (nZVI): Theory and application

Shaolin Li,Wei Wang,Feipeng Liang,Wei-xian Zhang

Treatment of wastewater containing heavy metals requires considerations on simultaneous removal of different ions, system reliability and quick separation of reaction products. In this work, we demonstrate that nanoscale zero-valent iron (nZVI) is an ideal reagent for removing heavy metals from wastewater. Batch experiments show that nZVI is able to perform simultaneous removal of different heavy metals and arsenic; reactive nZVI in uniform dispersion brings rapid changes in solution E h , enabling a facile way for reaction regulation. Microscope characterizations and settling experiments suggest that nZVI serves as solid seeds that facilitate products separation. A treatment process consisting of E h -controlled nZVI reaction, gravitational separation and nZVI recirculation is then demonstrated. Long-term (>12 months) operation shows that the process achieves >99.5% removal of As, Cu and a number of other toxic elements. The E h -controlled reaction system sustains a highly-reducing condition in reactor and reduces nZVI dosage. The process produces effluent of stable quality that meets local discharge guidelines. The gravitational separator shows high efficacy of nZVI recovery and the recirculation improves nZVI material efficiency, resulting in extraordinarily high removal capacities ((245   mg As   +   226 mg-Cu)/g-nZVI). The work provides proof that nanomaterials can offer truly green and cost-effective solutions for wastewater treatment.

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CHEMOSPHERE · 2015 · IF 3.34

Novel iron metal matrix composite reinforced by quartz sand for the effective dechlorination of aqueous 2-chlorophenol

Yunfei Zhang,Bo Yang,Yanni Han,Chaojin Jiang,Deli Wu,Jinhong Fan,Luming Ma

In this work, we tested a novel iron metal matrix composite (MMC) synthesized by mechanically introducing quartz sand (SiO 2 ) into an iron matrix (denoted as SiO 2 –Fe MMC). The pseudo-first-order reaction rate constant of the SiO 2 –Fe MMC (initial pH 5.0) for 20 mg/L of 2-chlorophenol (2-CP) was 0.051 × 10 −3  L/m 2 /min, which was even higher than that of some reported Pd/Fe bimetals. This extraordinary high activity was promoted by the quick iron dissolution rate, which was caused by the formation of Fe–C internal electrolysis from carbonization of process control agent (PCA) and the active reinforcement/metal interfaces during the milling process. In addition, pH has slight effect on the dechlorination rate. The SiO 2 –Fe MMC retained relatively stable activity, still achieving 71% removal efficiency for 2-CP after six consecutive cycles. The decrease in dechlorination efficiency can be attributed to the rapid consumption of Fe 0 . A dechlorination mechanism using the SiO 2 –Fe MMC was proposed by a direct electron transfer from Fe 0 to 2-CP at the quartz sand/iron interface.

CAS / MDL: 7782-63-0 7439-89-6
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RSC Advances · 2017 ·Vol. 7 ·期 10 ·5621-5627 · IF 3.108

MIL-100(Fe)-catalyzed efficient conversion of hexoses to lactic acid

Shan Huang,Kai-Li Yang,Xiao-Fang Liu,Hu Pan,Heng Zhang,Song Yang

MIL-100(Fe) was used for the first time in the catalytic transformation of hexose sugars into lactic acid (LA). The as-synthesized MIL-100(Fe) was systematically characterized, and its superior morphological and textural properties were demonstrated to contribute greatly to the pronounced catalytic performance in fructose-to-LA conversion (up to 32% yield), as compared with other catalysts like Cu-BTC and MIL-100(Cr). The effects of reaction conditions including temperature, reaction time, and substrate loading were explored. In addition, MIL-100(Fe) could be easily reused for 4 cycles with no evident decrease in catalytic activity.

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RSC Advances · 2016 ·Vol. 6 ·期 80 ·76867-76873 · IF 3.289

A mechanically synthesized SiO2–Fe metal matrix composite for effective dechlorination of aqueous 2-chlorophenol: the optimum of the preparation conditions

Yunfei Zhang,Bo Yang,Jinhong Fan,Luming Ma

In this study, abrasives-reinforced metal matrix composites (MMCs) with a microscale size synthesized by ball milling (BM) could achieve highly active and stable dechlorination efficiency for aqueous 2-chlorophenol (2-CP). The preparation process of this composite via BM was optimized to obtain a high degradation efficiency, especially for the effect of the abrasives including B4C, SiC, α-Al2O3, SiO2, Fe3O4 and Na2SO4. The results showed that the hardness of the abrasives in the Fe-based MMCs was closely related with their dechlorination performance. Subsequently, the optimal abrasive, i.e. SiO2 was further investigated for its proper milling conditions with zero-valent iron (ZVI) particles including optimal SiO2 size, SiO2 loading, milling time, and the dosage of the process control agent (PCA). Additionally, the influence of other metal categories including Al and Si was also investigated for dechlorination; and their low reaction efficiencies were closely related with their passivating film. Finally, the longevity test suggested that the decreased reactivity of the SiO2–Fe MMC during the storage in air could be recovered when consecutively used, mainly due to the promoting effects of the inherent structure of SiO2–Fe MMC with the Fe/C and Fe/SiO2 interfaces, as well as the effective regeneration of the reactive sites by continuous iron dissolution.

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BIORESOURCE TECHNOLOGY · 2017 · IF 5.651

Unraveling the impact of nanoscale zero-valent iron on the nitrogen removal performance and microbial community of anammox sludge

Zheng-Zhe Zhang,Jia-Jia Xu,Zhi-Jian Shi,Yu-Hui Bai,Ya-Fei Cheng,Hai-Yan Hu,Ren-Cun Jin

Given the increasing use of nanoscale zero-valent iron (NZVI) particles for environmental remediation and wastewater treatment, their potential impact on anaerobic ammonium oxidation (anammox) bacteria was investigated in this study using anammox sludge. Batch assays showed that NZVI concentrations up to 200   mg   L −1 did not affect anammox activity, reactive oxygen species production, and cell membrane integrity. The nitrogen removal efficiency of the continuous-flow reactor fluctuated in the presence of 20 or 50   mg   L −1 NZVI, but it could return to normal over time, even at 200   mg   L −1 NZVI. 16S rDNA-based high-throughput sequencing indicated that although the presence of 10, 20, 50, and 200   mg   L −1 NZVI to some extent affected microbial composition, the anammox bacteria ( Candidatus Kuenenia ) never lost its dominance. The abundance of gene families that are related to the assimilation and utilization of iron was down-regulated in response to the stress of high-level NZVI.

CAS / MDL: 7439-89-6
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