To understand the feasibility of its application to the in situ remediation of contaminated groundwater,the dechlori-nation of 2,4-dichlorophenol (2,4-DCP) by Ni/Fe nanoparticles in the presence of humic acid (HA) was...To understand the feasibility of its application to the in situ remediation of contaminated groundwater,the dechlori-nation of 2,4-dichlorophenol (2,4-DCP) by Ni/Fe nanoparticles in the presence of humic acid (HA) was investigated.We found that,as high performance liquid chromatography (HPLC) was used,the 2,4-DCP was first quickly reduced to o-chlorophenol (o-CP) and p-chlorophenol (p-CP),and then reduced to phenol as the final product.Our experimental results indicated that HA had an adverse effect on the dechlorination of 2,4-DCP by Ni/Fe nanoparticles,as the HA concentration increased,the removal rate decreased evidently.It also demonstrated that 2,4-DCP was reduced more easily to o-CP than to p-CP,and that the sequence of the tendency in dechlorination of intermediates was p-CP>o-CP.Transmission electron microscope (TEM) showed that HA could act as an adsorbate to compete reactive sites on the surface of Ni/Fe nanoparticles to decrease the dechlorination rate.Also we con-cluded that the dechlorination reaction of 2,4-DCP over Ni/Fe nanoparticles progressed through catalytic reductive dechlorination.展开更多
The DBSA-PANI-Fe composite powder with 50wt% of Fe nanoparticles was prepared by mechanically mixing the DBSA-doped polyaniline powder and Fe nanoparticles. The composite powder was compacted to pellets and the pellet...The DBSA-PANI-Fe composite powder with 50wt% of Fe nanoparticles was prepared by mechanically mixing the DBSA-doped polyaniline powder and Fe nanoparticles. The composite powder was compacted to pellets and the pellets were annealed in vacuum at 443,493,543, and 593 K for 60 and 120 min. The conductivity of the pellet increases markedly with increasing the annealing temperature up to 493 K, and then decreases with further increasing the annealing temperature. When the pellet was annealed at 493 K for 60 min, the increment of conductivity reaches a maximum value, and the conductivity is 2.6 times as large as that of the pellet unannealed. The conductivities of the pellets annealed under the conditions of 543 K/120 min, 593 K/60 min, and 593 K/120 min are lower than the conductivity of the pellet unannealed. For all the pellets, the variation in conductivity with temperature reveals that the charge transport mechanism can be considered to be 1-D variable-range-hopping （1-D VRH）. The composite pellet shows a magnetic hysteresis loop independent of the annealing condition. The saturation magnetization is about 5.4×10^4 emu/kg. The saturation field and the coercivity are estimated to be 4.38×10^5 and 3.06×10^4 A/m, respectively. The crystalline structure ofFe nanoparticles in the composites does not change with the annealing condition. The annealing condition cannot destroy the polymer backbones.展开更多
Chlorinated phenols are a kind of environmental priority pollutants that attract much attention. The effect of Ni on the removal of pentachlorophenol （PCP） with Fe nanoparticles was investigated in this study. Fe na...Chlorinated phenols are a kind of environmental priority pollutants that attract much attention. The effect of Ni on the removal of pentachlorophenol （PCP） with Fe nanoparticles was investigated in this study. Fe nanoparticles and Ni submicron particles were synthesized using chemical reduction method and wet chemical techniques, respectively. And the concentrations of PCP and chloride ion in solutions were measured with and without Ni present. The results showed that the dechlorination of PCP was promoted in the presence of Ni particles, and the dechlorination efficiency was reduced along with the increase of Ni size. When the diameter of Ni particle was smaller than 300 nm, the removal efficiency of PCP was obviously increased in the initial 4 h, and then became the similar to that of the system with Fe only. When the diameter of Ni particle was between 400 nm and 1 μm, the removal efficiency of PCP was increased in the initial 1 h. Then the removal of PCP was inhibited, and the inhibition was increased with the increase of Ni size. Later, the removal efficiency was the similar in various systems.展开更多
Rational design and synthesis of non-precious-metal catalyst plays an important role in improving the activity and stability for oxygen reduction reaction(ORR)but remains a major challenge.In this work,we used a facil...Rational design and synthesis of non-precious-metal catalyst plays an important role in improving the activity and stability for oxygen reduction reaction(ORR)but remains a major challenge.In this work,we used a facile approach to synthesize iron nanoparticles encapsulated in nitrogen-doped porous carbon materials(Fe@N-C)from functionalized metal-organic frameworks(MOFs,MET-6).Embedding Fe nanoparticles into the carbon skeleton increases the graphitization degree and the proportion of graphitic N as well as promotes the formation of mesopores in the catalyst.The Fe@N-C-30 catalyst showed the excellent ORR activity in alkaline solutions(E^(0)=0.97 V vs.RHE,E1/2=0.89 V vs.RHE).Moreover,the Fe@N-C-30 catalyst exhibited better methanol resistance and long-term stability when compared to commercial Pt/C.The superior ORR performance could be attributed to the combination of high electrochemical surface area,relative high portion of graphitic-N,unique porous structures and the synergistic effect between the encapsulated Fe particles and the N-doped carbon layer.This work provides a promising method to construct efficient non-precious-metal ORR catalyst through MOFs.展开更多
Ferromagnetic Fe3O4 nanoparticles were synthesized using water as the solvent through the sol-gel method, which was selected for its cost-effectiveness, simplicity, and eco-friendly nature. The synthesized nanoparticl...Ferromagnetic Fe3O4 nanoparticles were synthesized using water as the solvent through the sol-gel method, which was selected for its cost-effectiveness, simplicity, and eco-friendly nature. The synthesized nanoparticles were characterized using a variety of techniques, including Fourier Transform Infrared (FTIR) spectroscopy, X-ray powder diffraction (XRD), Scanning Electron Microscopy (SEM), Thermogravimetric Analysis (TGA), and Vibrating Sample Magnetometer (VSM). These characterizations confirmed the successful formation of Fe3O4 nanoparticles. The FTIR spectra identified characteristic peaks corresponding to the functional groups present, and XRD analysis, using Scherer’s equation, determined an average crystalline size of 1.2 nm for the Fe3O4 nanoparticles. TGA results demonstrated the thermal stability of the nanoparticles, SEM imaging revealed distinct honeycomb-like structures for the nanoparticles synthesized with water as the solvent, while the VSM analysis was used to determine the magnetic behavior of the nanoparticles.展开更多
Carbon encapsulated Fe nanoparticles were successfully prepared via confined arc plasma method. The composition, morphology, microstructure, specific surface area and particle size of the product were characterized vi...Carbon encapsulated Fe nanoparticles were successfully prepared via confined arc plasma method. The composition, morphology, microstructure, specific surface area and particle size of the product were characterized via X-ray diffraction, transmission electron microscopy, high resolution transmission electron microscopy, energy dispersive X-ray spectrometry and Brunauer-Emmett-Teller N2 adsorption. The experiment results show that the carbon encapsulated Fe nanoparticles have clear core-shell structure. The core of the particles is body centered cubic Fe, and the shell is disorder carbons. The particles are in spherical or ellipsoidal shapes. The particle size of the nanocapsules ranges from 15 to 40 nm, with the average value of about 30 nm. The particle diameter of the core is 18 nm, the thickness of the shells is 6-8 nm, and the specific surface area is 24 m2/g.展开更多
At present, there is little commercial sale of biochar, since farmers find they can not gain a return on their investment in this amendment in the first few years after its application, because of the high cost associ...At present, there is little commercial sale of biochar, since farmers find they can not gain a return on their investment in this amendment in the first few years after its application, because of the high cost associated with large application rates. To overcome this constraint, development of artificially aged enriched biochar-mineral complexes(BMCs), having a higher mineral content, surface functionality, exchangeable cations, high concentration of magnetic iron(Fe) nanoparticles, and higher water-extractable organic compounds has been undertaken by a combined team of researchers and a commercial company. Two biochars produced under different pyrolysis conditions were activated with a phosphoric acid treatment. A mixture of clay, chicken litter, and minerals were added to the biochar, and then this composite was torrefied at either 180 or 220?C. In this study a pot experiment was carried out in glasshouse conditions to determine the effects of four different BMCs, with different formulations applied at rates of 100 and 200 kg ha-1, on the mycorrhizal colonisation, wheat growth and nutrient uptake, and soil quality improvement. It was found that the phosphorus(P) and nitrogen uptake in wheat shoots were significantly greater for a low application rate of BMCs(100 kg ha-1). The present formulation of BMC was effective in enhancing growth of wheat at low application rate(100 kg ha-1). The increase in growth appeared due to an increase in P uptake in the plants that could be partly attributed to an increase in mycorrhizal colonisation and partly due to the properties of the BMC.展开更多
Using a liquid-solid phase inversion method, a hybrid matrix poly（vinylidene fluoride）（PVDF） membrane was prepared with alumina（Al2O3） nanoparticle addition. Pd/Fe nanoparticles（NPs） were successfully immobili...Using a liquid-solid phase inversion method, a hybrid matrix poly（vinylidene fluoride）（PVDF） membrane was prepared with alumina（Al2O3） nanoparticle addition. Pd/Fe nanoparticles（NPs） were successfully immobilized on the Al2O3/PVDF membrane, which was characterized by Scanning Electron Microscopy（SEM） and Transmission Electron Microscopy（TEM）. The micrographs showed that the Pd/Fe NPs were dispersed homogeneously. Several important experimental parameters were optimized, including the mechanical properties, contact angle and surface area of Al2O3/PVDF composite membranes with different Al2O3 contents. At the same time, the ferrous ion concentration and the effect of hydrophilization were studied. The results showed that the modified Al2O3/PVDF membrane functioned well as a support. The Al2O3/PVDF membrane with immobilized Pd/Fe NPs exhibited high efficiency in terms of dichloroacetic acid（DCAA） dechlorination. Additionally, a reaction pathway for DCAA dechlorination by Pd/Fe NPs immobilized on the Al2O3/PVDF membrane system was proposed.展开更多
Highly biocompatible superparamagnetic Fe3O4 nanoparticles were synthesized by amide of folic acid （FA） ligands and the NH2-group onto the surface of Fe3O4 nanoparticles. The as-synthesized folate-conjugated Fe3O4 n...Highly biocompatible superparamagnetic Fe3O4 nanoparticles were synthesized by amide of folic acid （FA） ligands and the NH2-group onto the surface of Fe3O4 nanoparticles. The as-synthesized folate-conjugated Fe3O4 nanoparticles were characterized by X-ray diffraction diffractometer, transmission electron microscope, FT-IR spectrometer, vibrating sample magnetometer, and dynamic light scattering instrument. The in vivo labeling effect of folate-conjugated Fe3O4 nanoparticles on the hepatoma cells was investigated in tumor-bearing rat. The results demonstrate that the as-prepared nanoparticles have cubic structure of Fe3O4 with a particle size of about 8 nm and hydrated diameter of 25.7 nm at a saturation magnetization of 51 A·m2/kg. These nanoparticles possess good physiological stability, low cytotoxicity on human skin fibroblasts and negligible effect on Wistar rats at the concentration as high as 3 mg/kg body mass. The folate-conjugated Fe3O4 nanoparticles could be effectively mediated into the human hepatoma Bel 7402 cells through the binding of folate and folic acid receptor, enhancing the signal contrast of tumor tissue and surrounding normal tissue in MRI imaging. It is in favor of the tumor cells labeling, tracing, magnetic resonance imaging （MRI） target detection and magnetic hyperthermia.展开更多
Irradiation with swift heavy ions causes the deformation of Ferric nanoparticles in direction of the ion beam.Fe nanoparticles with mean diameter of about 20 nm were prepared by gas flow sputtering and subsequently co...Irradiation with swift heavy ions causes the deformation of Ferric nanoparticles in direction of the ion beam.Fe nanoparticles with mean diameter of about 20 nm were prepared by gas flow sputtering and subsequently confined within silica films.Two silica films wherein two different densities of Fe nanoparticles are encapsulated were irradiated with 50 MeV Ag ions with fluences of few 1014 ions.cm^(-2) at 300 K and normal incidence.Transmission electron microscopy analysis shows that the spherical Fe nanoparticles are deformed into prolate nanorods aligned in direction of the incident ion beam.The depth distribution profiles of irradiated particles reveal the presence of a critical fluence above which the elongation kinetics becomes dependent on the nanoparticles density.Analysis indicates that for the lower density particles,a saturation length is reached under irradiation to fluence between 3-4×10^(14) ions.cm^(-2).However,for the higher density,collective growth into aligned nanowires is presumed to take place.Hysteresis curves of the saturation magnetization and coercivity indicate an increasing magnetic anisotropy,which can be correlated with the deformation of nanoparticles in the direction of the ion beam.展开更多
In this work, compressive, flexural and split tensile strength together with coefficient of water absorption of high performance self-compacting concrete containing different amount of Fe2Os nanoparticles have been in...In this work, compressive, flexural and split tensile strength together with coefficient of water absorption of high performance self-compacting concrete containing different amount of Fe2Os nanoparticles have been investigated. The strength and the water permeability of the specimens have been improved by adding Fe2Os nanoparticles in the cement paste up to 4.0 wt%. Fe203 nanoparticle as a foreign nucleation site could accelerate C-S-H gel formation as a result of increased crystalline Ca（OH）2 amount especially at the early age of hydration and hence increase the strength of the specimens. In addition, Fe203 nanoparticles are able to act as nanofillers and recover the pore structure of the specimens by decreasing harmful pores to improve the water permeability. Several empirical relations have been presented to predict the flexural and the split tensile strength of the specimens by means of the corresponding compressive strength at a certain age of curing. Accelerated peak appearance in conduction calorimetry tests, more weight loss in thermogravimetric analysis and more rapid appearance of peaks related to hydrated products in X-ray diffraction results indicate that Fe203 nanoparticles up to 4 wt% could improve the mechanical and the physical properties of the specimens.展开更多
Effective in situ remediation of Cr（VI） in groundwater requires the successful delivery of reactive iron particles to the subsurface. Fe 0 nanoparticles （20–110 nm diameter） supported on silica fume were synthesi...Effective in situ remediation of Cr（VI） in groundwater requires the successful delivery of reactive iron particles to the subsurface. Fe 0 nanoparticles （20–110 nm diameter） supported on silica fume were synthesized by borohydride reduction of an aqueous iron salt in the presence of a support material. The experimental result showed that attachment of Fe 0 nanoparticles on the commercial available sub-micrometer silica fume prevented them from aggregation while maintaining the particle reactivity. When the Fe 0 concentration was 0.4 g/L, 88.00% of 40 mg/L Cr（VI） was removed by silica fume-supported Fe 0 nanoparticles （SF-Fe 0 ） in 120 min, 22.55% higher than unsupported Fe 0 . Furthermore, transport experiments confirmed that almost all unsupported Fe 0 was retained, whereas 51.50% and 38.29% of SF-Fe 0 were eluted from the vertical and horizontal sand column, respectively. Additionally, the effect of solution ionic strength on the transport ability of SF-Fe 0 was evaluated. The result showed that increase in the salt concentration led to a decrease in the mobility and also the divalent ion Ca 2＋ had a greater effect than that of monovalent ion Na ＋ .展开更多
Peroxidase-like catalytic properties of Fe3O4 nanoparficles （NPs） with three different sizes, synthesized by chemical coprecipitation and sol-gel methods, were investigated by UV-vis spectrum analysis. By comparing ...Peroxidase-like catalytic properties of Fe3O4 nanoparficles （NPs） with three different sizes, synthesized by chemical coprecipitation and sol-gel methods, were investigated by UV-vis spectrum analysis. By comparing Fe3O4 NPs with average diameters of 11, 20, and 150 nm, we found that the catalytic activity increases with the reduced nanoparticle size. The electrochemical method to characterize the catalytic activity of Fe3O4 NPs using the response currents of the reaction product and substrate was also developed.展开更多
To improve the initial coulombic efficiency and bulk density of ordered mesoporous carbons, active Fe203 nanoparticles were introduced into tubular mesopore channels of CMK-5 carbon, which possesses high specific surf...To improve the initial coulombic efficiency and bulk density of ordered mesoporous carbons, active Fe203 nanoparticles were introduced into tubular mesopore channels of CMK-5 carbon, which possesses high specific surface area （〉1700 m2.g-1） and large pore volume （〉1.8 cm3-g-1）. Fine Fe203 nanoparticles with sizes in the range of 5-7 nm were highly and homogenously encapsulated into CMK-5 matrix through ammonia-treatment and subsequent pyrolysis method. The Fe203 loading was carefully tailored and designed to warrant a high Fe203 content and adequate buffer space for improving the electrochemical performance. In particular, such Fe203 and mesoporous carbon composite with 47 wt% loading exhibits a considerably stable cycle performance （683 mAh.g-1 after 100 cycles, 99% capacity retention against that of the second cycle） as well as good rate capability. The fabrication strategy can effectively solve the drawback of single material, and achieve a high-performance lithium electrode material.展开更多
The FeS coated Fe nanoparticles were prepared by using high temperature reactions between the commercial Fe nanoparticles and the S powders in a sealed quartz tube. The simple method developed in this work is effectiv...The FeS coated Fe nanoparticles were prepared by using high temperature reactions between the commercial Fe nanoparticles and the S powders in a sealed quartz tube. The simple method developed in this work is effective for large scale synthesis of FeS/Fe nanoparticles with tunable shell/core structures, which can be obtained by controlling the atomic ratio of Fe to S. The structural, magnetic and photocatalytic properties of the nanoparticles were investigated systematically. The good photocatalytic performance originating from the FeS shell in degradation of methylene blue under visible light and the high saturation magnetization originating from the ferromagnetic Fe core make the FeS/Fe nanoparticles a good photocatalyst that can be collected and recycled easily with a magnet. An exchange bias up to tl mT induced in Fe by FeS was observed in the Fe/FeS nanoparticles with ferro/antiferromagnetic interfaces. The enhanced coercivi- ty up to 32 mT was ascribed to the size effect of Fe core.展开更多
Fe3O4 nanoparticles were prepared by chemistry co-precipitation and the mean crystal size was 17.9 nm measured by XRD. After it had been treated by silane-coupling agents KH570, magnetic micro-spheres dispersed in org...Fe3O4 nanoparticles were prepared by chemistry co-precipitation and the mean crystal size was 17.9 nm measured by XRD. After it had been treated by silane-coupling agents KH570, magnetic micro-spheres dispersed in organic medium glycol were gained and the mean size of Fe3O4 nanopowders was 33.7 nm. So it can be concluded that magnetic micro-sphere is made of a few Fe3O4 crystals. Many factors of modification were researched, such as the time of ball milling, the content of Fe3O4 and the content of KH570. The modification of Fe3O4 is relative to the time of ball milling, but the dominant function is affected by the content of Fe3O4 and KH570. When the content of Fe3O4 is known, there is a suitable content of KH570. Different content of Fe3O4 will make the different suitable content of KH570, but the range of latter is less than former, which is relative to the distribution of KH570 on Fe3O4 surface or in the solution.展开更多
Cross-linkedβ-cyclodextrin polymer/Fe3O4 composite nanoparticles with core-shell structures were prepared via cross linking reaction on the surface of carboxymethylβ-cyclodextrin（CM-β-CD） modified Fe3O4 nanoparti...Cross-linkedβ-cyclodextrin polymer/Fe3O4 composite nanoparticles with core-shell structures were prepared via cross linking reaction on the surface of carboxymethylβ-cyclodextrin（CM-β-CD） modified Fe3O4 nanoparticles inβ-cyclodextrin alkaline solution by using epichlorohydrin as crosslinking agent.The morphology,structure and magnetic properties of the prepared composite nanoparticles were investigated by transmission electron microscopy（TEM）,Fourier transform infrared（FTIR） spectrometry,X-ray diffraction（XRD） measurement,thermogravimetric analysis（TGA） and Vibrating sample magnetometry （VSM）,respectively.展开更多
We proposed a new way to synthesize a nanocomposite consisted of cementite Fe3C nanoparticles and amorphous carbon by radio frequency plasma-enhanced chemical vapor deposition. Transmission electron microscope images ...We proposed a new way to synthesize a nanocomposite consisted of cementite Fe3C nanoparticles and amorphous carbon by radio frequency plasma-enhanced chemical vapor deposition. Transmission electron microscope images show the existence of nanometric dark grains（Fe3C） embedded in a light matrix（amorphous carbon） in the samples. X-ray photoelectron spectroscopy experiment exhibit that the chemical bonding state in the films corresponded to sp3/sp2 amorphous carbon, sp^3 C-N（287.3 eV） and C15 in Fe3C（283.5 eV）. With increasing deposition time, the ratio of amorphous carbon increased. The magnetic measurements show that the value of in-lane coercivity increased with increasing carbon matrix concentration（from about 6.56× 10^3 A/m for film without carbon structures to approximately 2.77× 10^4 and 5.81 × 10^4 AJm for nanocomposite films at room temperature and 10 K, respectively）. The values of saturation magnetization for the synthesized nanocomposites were lower than that of the bulk Fe3C （ 140 Am^2/kg）.展开更多
The surface organic modification of Fe3O4 nanoparticles with silane coupling reagent KH570 was studied. The modified and unmodified nanoparticles were characterized by FT-IR, XPS and TEM. The spectra of FT-IR and XPS ...The surface organic modification of Fe3O4 nanoparticles with silane coupling reagent KH570 was studied. The modified and unmodified nanoparticles were characterized by FT-IR, XPS and TEM. The spectra of FT-IR and XPS revealed that KH570 was coated onto the surface of Fe3O4 nanoparticles to get Fe-O- Si bond and an organic coating layer also was formed. Fe3O4 nanoparticles were spheres partly with mean size of 18,8 nm studied by TEM, which was consistent with the result 17.9 nm calculated by Scherrer＇s equation. KH570 was adsorbed on surface and formed chemistry bond to be steric hindrance repulsion which prevented nanoparticles from reuniting. Then glycol-based Fe3O4 magnetic liquids dispersed stably was gained.展开更多
Fe3O4 magnetic nanoparticles(MNPs) were synthesised, characterised, and used as a peroxidase mimetic to accelerate levofloxacin sono-degradation in an ultrasound(US)/H2O2 system. The Fe3O4 MNPs were in nanometre scale...Fe3O4 magnetic nanoparticles(MNPs) were synthesised, characterised, and used as a peroxidase mimetic to accelerate levofloxacin sono-degradation in an ultrasound(US)/H2O2 system. The Fe3O4 MNPs were in nanometre scale with an average diameter of approximately 12 to 18 nm. The introduction of Fe3O4 MNPs increased levofloxacin sono-degradation in the US/H2O2 system. Experimental parameters, such as Fe3O4 MNP dose, initial solution p H, and H2O2 concentration, were investigated by a one-factor-at-a-time approach. The results showed that Fe3O4 MNPs enhanced levofloxacin removal in the p H range from 4.0 to 9.0. Levofloxacin removal ratio increased with Fe3O4 MNP dose up to 1.0 g·L-1and with H2O2 concentration until reaching the maximum. Moreover, three main intermediate compounds were identified by HPLC with electrospray ionisation tandem mass spectrometry, and a possible degradation pathway was proposed. This study suggests that combination of H2O2, Fe3O4 MNPs and US is a good way to improve the degradation efficiency of antibiotics.展开更多
基金Project supported by the National Natural Science Foundation of China(No.20407015)the Program for New Century Excellent Talents in University(No.NCET-06-0525),China
文摘To understand the feasibility of its application to the in situ remediation of contaminated groundwater,the dechlori-nation of 2,4-dichlorophenol (2,4-DCP) by Ni/Fe nanoparticles in the presence of humic acid (HA) was investigated.We found that,as high performance liquid chromatography (HPLC) was used,the 2,4-DCP was first quickly reduced to o-chlorophenol (o-CP) and p-chlorophenol (p-CP),and then reduced to phenol as the final product.Our experimental results indicated that HA had an adverse effect on the dechlorination of 2,4-DCP by Ni/Fe nanoparticles,as the HA concentration increased,the removal rate decreased evidently.It also demonstrated that 2,4-DCP was reduced more easily to o-CP than to p-CP,and that the sequence of the tendency in dechlorination of intermediates was p-CP>o-CP.Transmission electron microscope (TEM) showed that HA could act as an adsorbate to compete reactive sites on the surface of Ni/Fe nanoparticles to decrease the dechlorination rate.Also we con-cluded that the dechlorination reaction of 2,4-DCP over Ni/Fe nanoparticles progressed through catalytic reductive dechlorination.
基金the Education Reform Foundation of University of Science and Technology Beijing (No.00008099)
文摘The DBSA-PANI-Fe composite powder with 50wt% of Fe nanoparticles was prepared by mechanically mixing the DBSA-doped polyaniline powder and Fe nanoparticles. The composite powder was compacted to pellets and the pellets were annealed in vacuum at 443,493,543, and 593 K for 60 and 120 min. The conductivity of the pellet increases markedly with increasing the annealing temperature up to 493 K, and then decreases with further increasing the annealing temperature. When the pellet was annealed at 493 K for 60 min, the increment of conductivity reaches a maximum value, and the conductivity is 2.6 times as large as that of the pellet unannealed. The conductivities of the pellets annealed under the conditions of 543 K/120 min, 593 K/60 min, and 593 K/120 min are lower than the conductivity of the pellet unannealed. For all the pellets, the variation in conductivity with temperature reveals that the charge transport mechanism can be considered to be 1-D variable-range-hopping （1-D VRH）. The composite pellet shows a magnetic hysteresis loop independent of the annealing condition. The saturation magnetization is about 5.4×10^4 emu/kg. The saturation field and the coercivity are estimated to be 4.38×10^5 and 3.06×10^4 A/m, respectively. The crystalline structure ofFe nanoparticles in the composites does not change with the annealing condition. The annealing condition cannot destroy the polymer backbones.
基金Supported by the National Natural Science Foundation(51108454)
文摘Chlorinated phenols are a kind of environmental priority pollutants that attract much attention. The effect of Ni on the removal of pentachlorophenol （PCP） with Fe nanoparticles was investigated in this study. Fe nanoparticles and Ni submicron particles were synthesized using chemical reduction method and wet chemical techniques, respectively. And the concentrations of PCP and chloride ion in solutions were measured with and without Ni present. The results showed that the dechlorination of PCP was promoted in the presence of Ni particles, and the dechlorination efficiency was reduced along with the increase of Ni size. When the diameter of Ni particle was smaller than 300 nm, the removal efficiency of PCP was obviously increased in the initial 4 h, and then became the similar to that of the system with Fe only. When the diameter of Ni particle was between 400 nm and 1 μm, the removal efficiency of PCP was increased in the initial 1 h. Then the removal of PCP was inhibited, and the inhibition was increased with the increase of Ni size. Later, the removal efficiency was the similar in various systems.
基金supported by the National Natural Science Foundation of China(Grants 22002121,22172121)the National Undergraduate Training Program for Innovation and Entrepreneurship(Grant S202210656087).
文摘Rational design and synthesis of non-precious-metal catalyst plays an important role in improving the activity and stability for oxygen reduction reaction(ORR)but remains a major challenge.In this work,we used a facile approach to synthesize iron nanoparticles encapsulated in nitrogen-doped porous carbon materials(Fe@N-C)from functionalized metal-organic frameworks(MOFs,MET-6).Embedding Fe nanoparticles into the carbon skeleton increases the graphitization degree and the proportion of graphitic N as well as promotes the formation of mesopores in the catalyst.The Fe@N-C-30 catalyst showed the excellent ORR activity in alkaline solutions(E^(0)=0.97 V vs.RHE,E1/2=0.89 V vs.RHE).Moreover,the Fe@N-C-30 catalyst exhibited better methanol resistance and long-term stability when compared to commercial Pt/C.The superior ORR performance could be attributed to the combination of high electrochemical surface area,relative high portion of graphitic-N,unique porous structures and the synergistic effect between the encapsulated Fe particles and the N-doped carbon layer.This work provides a promising method to construct efficient non-precious-metal ORR catalyst through MOFs.
文摘Ferromagnetic Fe3O4 nanoparticles were synthesized using water as the solvent through the sol-gel method, which was selected for its cost-effectiveness, simplicity, and eco-friendly nature. The synthesized nanoparticles were characterized using a variety of techniques, including Fourier Transform Infrared (FTIR) spectroscopy, X-ray powder diffraction (XRD), Scanning Electron Microscopy (SEM), Thermogravimetric Analysis (TGA), and Vibrating Sample Magnetometer (VSM). These characterizations confirmed the successful formation of Fe3O4 nanoparticles. The FTIR spectra identified characteristic peaks corresponding to the functional groups present, and XRD analysis, using Scherer’s equation, determined an average crystalline size of 1.2 nm for the Fe3O4 nanoparticles. TGA results demonstrated the thermal stability of the nanoparticles, SEM imaging revealed distinct honeycomb-like structures for the nanoparticles synthesized with water as the solvent, while the VSM analysis was used to determine the magnetic behavior of the nanoparticles.
基金Project(208151)supported by the Key Project of Ministry of Education,ChinaProject(1014RJZA035)supported by the Natural Science Foundation of Gansu Province,China
文摘Carbon encapsulated Fe nanoparticles were successfully prepared via confined arc plasma method. The composition, morphology, microstructure, specific surface area and particle size of the product were characterized via X-ray diffraction, transmission electron microscopy, high resolution transmission electron microscopy, energy dispersive X-ray spectrometry and Brunauer-Emmett-Teller N2 adsorption. The experiment results show that the carbon encapsulated Fe nanoparticles have clear core-shell structure. The core of the particles is body centered cubic Fe, and the shell is disorder carbons. The particles are in spherical or ellipsoidal shapes. The particle size of the nanocapsules ranges from 15 to 40 nm, with the average value of about 30 nm. The particle diameter of the core is 18 nm, the thickness of the shells is 6-8 nm, and the specific surface area is 24 m2/g.
基金supported by Ven Earth LLC,San Francisco,CA,USA and the Australian Research Council
文摘At present, there is little commercial sale of biochar, since farmers find they can not gain a return on their investment in this amendment in the first few years after its application, because of the high cost associated with large application rates. To overcome this constraint, development of artificially aged enriched biochar-mineral complexes(BMCs), having a higher mineral content, surface functionality, exchangeable cations, high concentration of magnetic iron(Fe) nanoparticles, and higher water-extractable organic compounds has been undertaken by a combined team of researchers and a commercial company. Two biochars produced under different pyrolysis conditions were activated with a phosphoric acid treatment. A mixture of clay, chicken litter, and minerals were added to the biochar, and then this composite was torrefied at either 180 or 220?C. In this study a pot experiment was carried out in glasshouse conditions to determine the effects of four different BMCs, with different formulations applied at rates of 100 and 200 kg ha-1, on the mycorrhizal colonisation, wheat growth and nutrient uptake, and soil quality improvement. It was found that the phosphorus(P) and nitrogen uptake in wheat shoots were significantly greater for a low application rate of BMCs(100 kg ha-1). The present formulation of BMC was effective in enhancing growth of wheat at low application rate(100 kg ha-1). The increase in growth appeared due to an increase in P uptake in the plants that could be partly attributed to an increase in mycorrhizal colonisation and partly due to the properties of the BMC.
基金supported by the Nature Science Foundation of Heilongjiang Province (No. B201410)the Postdoctoral Foundation Project of Heilongjiang Province (No. LBH-Z13128)+3 种基金the Science and Technology Research Program of Education Bureau of Heilongjiang Province (No. 12531206)the Special Scientific Research Projects of Harbin Normal University (12XQXG02)the National Nature Science Foundation of China (No. 41030743)the National Nature Science Foundation of China (No. 42171217)
文摘Using a liquid-solid phase inversion method, a hybrid matrix poly（vinylidene fluoride）（PVDF） membrane was prepared with alumina（Al2O3） nanoparticle addition. Pd/Fe nanoparticles（NPs） were successfully immobilized on the Al2O3/PVDF membrane, which was characterized by Scanning Electron Microscopy（SEM） and Transmission Electron Microscopy（TEM）. The micrographs showed that the Pd/Fe NPs were dispersed homogeneously. Several important experimental parameters were optimized, including the mechanical properties, contact angle and surface area of Al2O3/PVDF composite membranes with different Al2O3 contents. At the same time, the ferrous ion concentration and the effect of hydrophilization were studied. The results showed that the modified Al2O3/PVDF membrane functioned well as a support. The Al2O3/PVDF membrane with immobilized Pd/Fe NPs exhibited high efficiency in terms of dichloroacetic acid（DCAA） dechlorination. Additionally, a reaction pathway for DCAA dechlorination by Pd/Fe NPs immobilized on the Al2O3/PVDF membrane system was proposed.
基金Project(2011JQ028)supported by the Fundamental Research Funds for the Central Universities,ChinaProjects(2008SK3114,2010SK3113)supported by Hunan Provincial Science&Technology Plan,China+2 种基金Project(B2007086)supported by Science&Research Funds of Hunan Health Department,ChinaProject(12JJ5057)supported by Natural Science Foundation of Hunan Province,ChinaProjects(XCX1119,XCX12073)supported by University Students Innovative Experiment Plan Project of Hunan Agricultural University,China
文摘Highly biocompatible superparamagnetic Fe3O4 nanoparticles were synthesized by amide of folic acid （FA） ligands and the NH2-group onto the surface of Fe3O4 nanoparticles. The as-synthesized folate-conjugated Fe3O4 nanoparticles were characterized by X-ray diffraction diffractometer, transmission electron microscope, FT-IR spectrometer, vibrating sample magnetometer, and dynamic light scattering instrument. The in vivo labeling effect of folate-conjugated Fe3O4 nanoparticles on the hepatoma cells was investigated in tumor-bearing rat. The results demonstrate that the as-prepared nanoparticles have cubic structure of Fe3O4 with a particle size of about 8 nm and hydrated diameter of 25.7 nm at a saturation magnetization of 51 A·m2/kg. These nanoparticles possess good physiological stability, low cytotoxicity on human skin fibroblasts and negligible effect on Wistar rats at the concentration as high as 3 mg/kg body mass. The folate-conjugated Fe3O4 nanoparticles could be effectively mediated into the human hepatoma Bel 7402 cells through the binding of folate and folic acid receptor, enhancing the signal contrast of tumor tissue and surrounding normal tissue in MRI imaging. It is in favor of the tumor cells labeling, tracing, magnetic resonance imaging （MRI） target detection and magnetic hyperthermia.
文摘Irradiation with swift heavy ions causes the deformation of Ferric nanoparticles in direction of the ion beam.Fe nanoparticles with mean diameter of about 20 nm were prepared by gas flow sputtering and subsequently confined within silica films.Two silica films wherein two different densities of Fe nanoparticles are encapsulated were irradiated with 50 MeV Ag ions with fluences of few 1014 ions.cm^(-2) at 300 K and normal incidence.Transmission electron microscopy analysis shows that the spherical Fe nanoparticles are deformed into prolate nanorods aligned in direction of the incident ion beam.The depth distribution profiles of irradiated particles reveal the presence of a critical fluence above which the elongation kinetics becomes dependent on the nanoparticles density.Analysis indicates that for the lower density particles,a saturation length is reached under irradiation to fluence between 3-4×10^(14) ions.cm^(-2).However,for the higher density,collective growth into aligned nanowires is presumed to take place.Hysteresis curves of the saturation magnetization and coercivity indicate an increasing magnetic anisotropy,which can be correlated with the deformation of nanoparticles in the direction of the ion beam.
文摘In this work, compressive, flexural and split tensile strength together with coefficient of water absorption of high performance self-compacting concrete containing different amount of Fe2Os nanoparticles have been investigated. The strength and the water permeability of the specimens have been improved by adding Fe2Os nanoparticles in the cement paste up to 4.0 wt%. Fe203 nanoparticle as a foreign nucleation site could accelerate C-S-H gel formation as a result of increased crystalline Ca（OH）2 amount especially at the early age of hydration and hence increase the strength of the specimens. In addition, Fe203 nanoparticles are able to act as nanofillers and recover the pore structure of the specimens by decreasing harmful pores to improve the water permeability. Several empirical relations have been presented to predict the flexural and the split tensile strength of the specimens by means of the corresponding compressive strength at a certain age of curing. Accelerated peak appearance in conduction calorimetry tests, more weight loss in thermogravimetric analysis and more rapid appearance of peaks related to hydrated products in X-ray diffraction results indicate that Fe203 nanoparticles up to 4 wt% could improve the mechanical and the physical properties of the specimens.
基金supported by the National Natural Science Foundation of China (No. 40971254)the National Youth Science Foundation of China (No. 20907023)
文摘Effective in situ remediation of Cr（VI） in groundwater requires the successful delivery of reactive iron particles to the subsurface. Fe 0 nanoparticles （20–110 nm diameter） supported on silica fume were synthesized by borohydride reduction of an aqueous iron salt in the presence of a support material. The experimental result showed that attachment of Fe 0 nanoparticles on the commercial available sub-micrometer silica fume prevented them from aggregation while maintaining the particle reactivity. When the Fe 0 concentration was 0.4 g/L, 88.00% of 40 mg/L Cr（VI） was removed by silica fume-supported Fe 0 nanoparticles （SF-Fe 0 ） in 120 min, 22.55% higher than unsupported Fe 0 . Furthermore, transport experiments confirmed that almost all unsupported Fe 0 was retained, whereas 51.50% and 38.29% of SF-Fe 0 were eluted from the vertical and horizontal sand column, respectively. Additionally, the effect of solution ionic strength on the transport ability of SF-Fe 0 was evaluated. The result showed that increase in the salt concentration led to a decrease in the mobility and also the divalent ion Ca 2＋ had a greater effect than that of monovalent ion Na ＋ .
基金This work was supported by the National Natural Science Foundation of China （Nos. 90406023 and 60571031）；National Important Science Research Program of China （Nos. 2006CB933206 and 2006CB705606）.
文摘Peroxidase-like catalytic properties of Fe3O4 nanoparficles （NPs） with three different sizes, synthesized by chemical coprecipitation and sol-gel methods, were investigated by UV-vis spectrum analysis. By comparing Fe3O4 NPs with average diameters of 11, 20, and 150 nm, we found that the catalytic activity increases with the reduced nanoparticle size. The electrochemical method to characterize the catalytic activity of Fe3O4 NPs using the response currents of the reaction product and substrate was also developed.
基金supported by the Fundamental Research Funds for the Central Universities (Grant No. DUT12ZD218)the National Natural Science Foundation of China (Grant No. 21103184)the Ph. D. Programs Foundation (Grant No. 20100041110017) of Ministry of Education of China
文摘To improve the initial coulombic efficiency and bulk density of ordered mesoporous carbons, active Fe203 nanoparticles were introduced into tubular mesopore channels of CMK-5 carbon, which possesses high specific surface area （〉1700 m2.g-1） and large pore volume （〉1.8 cm3-g-1）. Fine Fe203 nanoparticles with sizes in the range of 5-7 nm were highly and homogenously encapsulated into CMK-5 matrix through ammonia-treatment and subsequent pyrolysis method. The Fe203 loading was carefully tailored and designed to warrant a high Fe203 content and adequate buffer space for improving the electrochemical performance. In particular, such Fe203 and mesoporous carbon composite with 47 wt% loading exhibits a considerably stable cycle performance （683 mAh.g-1 after 100 cycles, 99% capacity retention against that of the second cycle） as well as good rate capability. The fabrication strategy can effectively solve the drawback of single material, and achieve a high-performance lithium electrode material.
文摘The FeS coated Fe nanoparticles were prepared by using high temperature reactions between the commercial Fe nanoparticles and the S powders in a sealed quartz tube. The simple method developed in this work is effective for large scale synthesis of FeS/Fe nanoparticles with tunable shell/core structures, which can be obtained by controlling the atomic ratio of Fe to S. The structural, magnetic and photocatalytic properties of the nanoparticles were investigated systematically. The good photocatalytic performance originating from the FeS shell in degradation of methylene blue under visible light and the high saturation magnetization originating from the ferromagnetic Fe core make the FeS/Fe nanoparticles a good photocatalyst that can be collected and recycled easily with a magnet. An exchange bias up to tl mT induced in Fe by FeS was observed in the Fe/FeS nanoparticles with ferro/antiferromagnetic interfaces. The enhanced coercivi- ty up to 32 mT was ascribed to the size effect of Fe core.
基金This work was financially supported by the Graduate Innovation Plan Projects of Jiangsu Province in 2005.
文摘Fe3O4 nanoparticles were prepared by chemistry co-precipitation and the mean crystal size was 17.9 nm measured by XRD. After it had been treated by silane-coupling agents KH570, magnetic micro-spheres dispersed in organic medium glycol were gained and the mean size of Fe3O4 nanopowders was 33.7 nm. So it can be concluded that magnetic micro-sphere is made of a few Fe3O4 crystals. Many factors of modification were researched, such as the time of ball milling, the content of Fe3O4 and the content of KH570. The modification of Fe3O4 is relative to the time of ball milling, but the dominant function is affected by the content of Fe3O4 and KH570. When the content of Fe3O4 is known, there is a suitable content of KH570. Different content of Fe3O4 will make the different suitable content of KH570, but the range of latter is less than former, which is relative to the distribution of KH570 on Fe3O4 surface or in the solution.
基金financially supported by the Guangdong Natural Science Foundation(No.020891)
文摘Cross-linkedβ-cyclodextrin polymer/Fe3O4 composite nanoparticles with core-shell structures were prepared via cross linking reaction on the surface of carboxymethylβ-cyclodextrin（CM-β-CD） modified Fe3O4 nanoparticles inβ-cyclodextrin alkaline solution by using epichlorohydrin as crosslinking agent.The morphology,structure and magnetic properties of the prepared composite nanoparticles were investigated by transmission electron microscopy（TEM）,Fourier transform infrared（FTIR） spectrometry,X-ray diffraction（XRD） measurement,thermogravimetric analysis（TGA） and Vibrating sample magnetometry （VSM）,respectively.
基金Supported by the National Natural Science Foundation of China(No.50832001)the Science and Technology Develop-ment Program of Jilin Province, China(No.20070501)
文摘We proposed a new way to synthesize a nanocomposite consisted of cementite Fe3C nanoparticles and amorphous carbon by radio frequency plasma-enhanced chemical vapor deposition. Transmission electron microscope images show the existence of nanometric dark grains（Fe3C） embedded in a light matrix（amorphous carbon） in the samples. X-ray photoelectron spectroscopy experiment exhibit that the chemical bonding state in the films corresponded to sp3/sp2 amorphous carbon, sp^3 C-N（287.3 eV） and C15 in Fe3C（283.5 eV）. With increasing deposition time, the ratio of amorphous carbon increased. The magnetic measurements show that the value of in-lane coercivity increased with increasing carbon matrix concentration（from about 6.56× 10^3 A/m for film without carbon structures to approximately 2.77× 10^4 and 5.81 × 10^4 AJm for nanocomposite films at room temperature and 10 K, respectively）. The values of saturation magnetization for the synthesized nanocomposites were lower than that of the bulk Fe3C （ 140 Am^2/kg）.
基金the Natural Science Fund of Jiangsu province (No.BK2007586)Jiangsu Planned Projects(No.0701012B)for Postdoctoral Research Funds
文摘The surface organic modification of Fe3O4 nanoparticles with silane coupling reagent KH570 was studied. The modified and unmodified nanoparticles were characterized by FT-IR, XPS and TEM. The spectra of FT-IR and XPS revealed that KH570 was coated onto the surface of Fe3O4 nanoparticles to get Fe-O- Si bond and an organic coating layer also was formed. Fe3O4 nanoparticles were spheres partly with mean size of 18,8 nm studied by TEM, which was consistent with the result 17.9 nm calculated by Scherrer＇s equation. KH570 was adsorbed on surface and formed chemistry bond to be steric hindrance repulsion which prevented nanoparticles from reuniting. Then glycol-based Fe3O4 magnetic liquids dispersed stably was gained.
基金Supported by the National Natural Science Foundation of China(51009115)Shaanxi Provincial Department of Education Key Laboratory Project(13JS067)+2 种基金the Hall of Shaanxi Province Science and Technology(2013JK0881)the Research Plan Project of Water Resources Department of Shaanxi Province(2013slkj-07)the Innovation of Science and Technology Fund of Xi'an University of Technology(211302)
文摘Fe3O4 magnetic nanoparticles(MNPs) were synthesised, characterised, and used as a peroxidase mimetic to accelerate levofloxacin sono-degradation in an ultrasound(US)/H2O2 system. The Fe3O4 MNPs were in nanometre scale with an average diameter of approximately 12 to 18 nm. The introduction of Fe3O4 MNPs increased levofloxacin sono-degradation in the US/H2O2 system. Experimental parameters, such as Fe3O4 MNP dose, initial solution p H, and H2O2 concentration, were investigated by a one-factor-at-a-time approach. The results showed that Fe3O4 MNPs enhanced levofloxacin removal in the p H range from 4.0 to 9.0. Levofloxacin removal ratio increased with Fe3O4 MNP dose up to 1.0 g·L-1and with H2O2 concentration until reaching the maximum. Moreover, three main intermediate compounds were identified by HPLC with electrospray ionisation tandem mass spectrometry, and a possible degradation pathway was proposed. This study suggests that combination of H2O2, Fe3O4 MNPs and US is a good way to improve the degradation efficiency of antibiotics.
