Journal of Materials Chemistry C
·
2016
·Vol. 4
·期 32
·7614-7621
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IF 5.066
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
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2016
·Vol. 92
·期 3
·552-561
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IF 2.738
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
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CHEMICAL ENGINEERING JOURNAL
·
2016
·
IF 5.31
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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CHEMICAL ENGINEERING RESEARCH & DESIGN
·
2016
·
IF 2.525
Huanhuan Zhang,Xiaoyu Lan,Peng Bai,Xianghai Guo
Six water-tolerable metal-organic frameworks (MIL-101(Cr), MIL-100(Fe), MIL-100(Cr), MIL-53(Cr), MIL-96(Al), and UiO-66) were employed for the adsorptive removal of acetic acid from water. UiO-66 exhibited more potential as an acetic acid adsorbent than other five MOFs. UiO-66 was further investigated in the view of adsorption kinetics, isotherm, thermodynamics, and regeneration of the adsorbent. The analysis of film diffusion and intraparticle diffusion model suggested that larger acetic acid concentrations would cause higher effects of boundary layer, and the adsorption process was multiple steps. The kinetic results show that adsorption of acetic acid on UiO-66 fitted to pseudo-second-order model and was controlled by chemical adsorption. The adsorption isotherm of acetic acid on UiO-66 followed Freundlich isotherm, which indicated the presence of heterogeneous surface on UiO-66. The thermodynamic parameters (Δ G , Δ H and Δ S ) were also calculated, confirming that the adsorption of acetic acid on UiO-66 was spontaneously exothermic and decrease of disorder. The regeneration of UiO-66 was also demonstrated by washing with deionized water and ethanol. The adsorption capacity and XRD of UiO-66 did not change significantly even after three cycles. Therefore, UiO-66 can be a promising adsorbent for adsorptive removal of acetic acid from wastewater.
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Scientific Reports
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2017
·Vol. 7
·期 1
·1-9
·
IF 4.259
He Shichong,Zhu Lizhong
Sorptive landfill liners can prevent the migration of the leachate pollutants. However, their sorption ability will decrease over time. A method should be developed to maintain the sorption ability of landfill liners. In this study, we combined cetyltrimethylammonium bromide-bentonite (CTMAB-bentonite) and zero-valent iron (ZVI) to develop a self-cleaning liner that can retain its sorption ability for a long period. Batch experiments and calculation simulations were employed to analyse the sorption ability of this liner material and the ecological risk of halogenated hydrocarbons. The results showed that CTMAB-bentonite could sorb halogenated hydrocarbons well, with saturated sorption capacities ( Q
m ) of 10.2, 14.5, 6.69, 18.5, 29.4, and 49.7 mg·g -1 for dichloroethane (DCA), trichloroethane (TCA), dichloroethene (DCE), trichloroethylene (TCE), tetrachloroethylene (PCE), and 1,3- dichloropropene (1,3-DCP), respectively. Using the mixture of 0.5 g iron and 0.5 g CTMAB-bentonite could dramatically increase the removal efficiency of DCE, TCE, and PCE. The reaction with ZVI did not change the structure of CTMAB-bentonite and its sorption ability remained consistent. Calculation results suggested that the self-cleaning landfill liner would dramatically decrease the hazard index (HI) of the eluate. However, the humic acid and salt in leachate would cause a reduction in the removal of halogenated hydrocarbons.
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PubMed
高影响因子
ANALYTICAL AND BIOANALYTICAL CHEMISTRY
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2016
·Vol. 408
·期 29
·8515-8528
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IF 3.125
Lu Nan,Wang Ting,Zhao Pan,Zhang Lianjun,Lun Xiaowen,Zhang Xueli,Hou Xiaohong
In the presented work, metal-organic framework (MOF) material MIL-101(Cr) (MIL, Matérial Institute Lavoisier) was used as a sorbent for vortex assisted dispersive micro-solid-phase extraction (VA-D-μ-SPE) of trace amount of metronidazole (MNZ), ronidazole (RNZ), secnidazole (SNZ), dimetridazole (DMZ), tinidazole (TNZ), and ornidazole (ONZ) in different environmental water samples. Ultra-high-performance liquid chromatography coupled with tandem mass spectrometry (UPLC-MS/MS) was used to quantify the target analytes. The extraction conditions, including type of sorbents, amount of MIL-101(Cr), solution pH, extraction method, extraction time, effect of salt, and elution conditions were investigated. Upon the optimal conditions, the developed method showed an excellent extraction performance with the average recovery ranging from 75.2 to 98.8 %. Good sensitivity levels were achieved with the detection limits of 0.03∼0.06 μg/L and the quantitation limits of 0.09∼0.20 μg/L. The linear ranges were varied from 0.1 to 20 for SNZ and ONZ and from 0.2 to 40 μg/L for MNZ, RNZ, DMZ, and TNZ ( r
2 > 0.992), and repeatability of the method was satisfactory with the relative standard deviations (RSD) <8 %. Ultimately, the applicability of the method was successfully confirmed by the extraction and determination of 5-nitroimidazoles (5-NDZs) in 12 real water samples, showing the positive findings of MNZ and TNZ ranging from 0.3 to 1.0 μg/L. Furthermore, molecular docking was applied to explain the molecular interactions and free binding energies between MIL-101(Cr) and 5-NDZs, providing a deep insight into the adsorption mechanism. The proposed method exhibited the advantages of simplicity, rapidly, less solvent consumption, ease of operation, higher sensitivity, and lower matrix effect.
Schematic diagram of the extraction process and molecular docking investigation
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JOURNAL OF HAZARDOUS MATERIALS
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2017
·
IF 6.065
Weizhao Yin,Yongtao Li,Jinhua Wu,Guocai Chen,Gangbiao Jiang,Ping Li,Jingjing Gu,Hao Liang,Chuansheng Liu
A one-pot bio-iron system was established to investigate synergetic abiotic and biotic effects between iron and microorganisms on Cr(VI) removal. More diverse iron corrosion and reactive solids, such as green rusts, lepidocrocite and magnetite were found in the bio-iron system than in the Fe 0 -H 2 O system, leading to 4.3 times higher Cr(VI) removal efficiency in the bio-iron system than in the Fe 0 -H 2 O system. The cycling experiment also showed that the Cr(VI) removal capacity of Fe 0 in the bio-iron system was 12.4 times higher than that in the Fe 0 -H 2 O system. A 62 days of life-span could be achieved in the bio-iron system, while the Fe 0 -H 2 O system lost its efficacy after 30 days. Enhanced effects of extra Fe 2+ on Cr(VI) removal was observed, largely contributed to the adsorbed Fe 2+ on iron surface, which could function as an extra reductant for Cr(VI) and promote the electron transfer on the solid phase. The results also showed that the reduction of Cr(VI) by microorganisms was insignificant, indicating the adsorption/co-precipitation of Cr by iron oxides on iron surface was responsible for the overall Cr(VI) removal. Our study demonstrated that the bio-amended iron corrosion could improve the performance of Fe 0 for Cr(VI) removal from groundwater.
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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
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2017
·Vol. 24
·期 22
·18640-18650
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IF 2.741
Chen Yuan,Lei Xin,Dou Rongni,Chen Yuancai,Hu Yongyou,Zhang Zhiqi
A water-compatible magnetic triclosan (TCS) imprinted material (TCS-CTS-Fe 0 -MIPs) was synthesized for selective enrichment and detection of TCS in real complex water samples. The material was synthesized by using chitosan (CTS) as functional monomer, which has rich surface O- and N-containing functional groups. The TCS imprinted CTS was coated on Fe 0 surface and then cross-linked with glutaraldehyde. Scanning electron microscopy suggested that the imprinted material was covered with a layer of imprinted film, Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy confirmed that the imprinted material had more functional groups (amino and hydroxyl groups) than that of non-imprinted material. The TCS imprinted and non-imprinted materials used in each adsorption experiments were 0.1 mg mL −1 . The maximum adsorption capacity of the TCS imprinted material and non-TCS imprinted material were 20.86 and 15.11 mg g −1 , respectively. The adsorption results showed that selectivity coefficient was 10.151, 1.353, and 8.271 in the presence of p-chlorophenol, 2,4,6-trichlorophenol, and bisphenol-A, respectively. The recoveries of river water and lake water samples were 92.8, 91.3, 92.4, and 81.4, 82.3, 82.1%, respectively, when the samples were spiked with 4, 6, and 8 μg L −1 of TCS with the imprinted material. The adsorption capacity of the TCS imprinted material and non-TCS imprinted material lost 5.2 and 6.2% after six times of recycling. The high selectivity and excellent adsorption capacity of the imprinted material can be attributed to the presence of sterically complementary imprinted sites and high surface, which would also made it more accessible to TCS than that of non-imprinted material. The present study would provide an environmental friendly and convenient method for the removal and the monitoring of TCS in environmental water samples.
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RSC Advances
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2017
·Vol. 7
·期 10
·5621-5627
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IF 3.108
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
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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CERAMICS INTERNATIONAL
·
2017
·
IF 2.986
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.
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FUEL
·
2024
·
IF 6.7
Ruonan Wang,Naif Abdullah Al-Dhabi,Yufeng Jiang,Xiaofeng Dai,Rui Li,Wangwang Tang,Rongbo Guo,Shanfei Fu
Food waste (FW) is prone to accumulate volatile fatty acids (VFAs) during anaerobic digestion (AD). In this study, nano zero-valent iron (nZVI) was used to enhance AD system stability and improve methane production efficiency. Results showed that nZVI facilitated the AD obviously. The highest cumulative methane production of 195.63 ± 5.38 mL/g VS was obtained at the nZVI dosage of 1.0 g/L, which was 22.6 % higher than that of the control. The appropriate addition of nZVI mainly strengthened the methanogenic stage of AD of FW, reduced the accumulation of VFAs and alleviated the pH fluctuation of the system. The corrosion hydrogen production efficiency of nZVI during AD first increased and then decreased with the increase of nZVI addition. Microbial community analysis demonstrated that the addition of nZVI mainly increased the abundance of hydrotropic methanogens and DIET-associated methanogens, and promoted the growth of bacteria in a symbiotic relationship with methanogens. In summary, the nZVI addition supplied a promising approach to improve the methane production efficiency from AD of FW.
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