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Sample records for fe3o4 polymer composites

  1. Preparation and characterization of cross-linked β-cyclodextrin polymer/Fe3O4 composite nanoparticles with core-shell structures

    Institute of Scientific and Technical Information of China (English)

    Rui Xue Li; Shu Mei Liu; Jian Qing Zhao; Hideyuki Otsuka; Atsushi Takahara

    2011-01-01

    Cross-linked β-cyclodextrin polymer/Fe3O4 composite nanoparticles with core-shell structures were prepared via cross linking reaction on the surface of carboxymethyl β-cyclodextrin (CM-β-CD) modified Fe3O4 nanoparticles in β-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.

  2. Core-Shell Ferromagnetic Nanorod Based on Amine Polymer Composite (Fe3O4@DAPF) for Fast Removal of Pb(II) from Aqueous Solutions.

    Science.gov (United States)

    Venkateswarlu, Sada; Yoon, Minyoung

    2015-11-18

    Heavy metal ion removal from wastewater constitutes an important issue in the water treatment industry. Although a variety of nanomaterials have been developed for heavy metal removal via adsorption, the adsorption capacity, removal efficiency, and material recyclability still remain a challenge. Here, we present novel Fe3O4@DAPF core-shell ferromagnetic nanorods (CSFMNRs) for the removal of Pb(II) from aqueous solutions; they were prepared by the facile surface modification of twin-like ferromagnetic Fe3O4 nanorods using a 2,3-diaminophenol and formaldehyde (DAPF)-based polymer. The crystallinity and structure of the Fe3O4 nanorods were confirmed via X-ray diffraction (XRD). Transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS) revealed the core-shell morphology and composition of the materials. Pb(II) removal using the prepared Fe3O4@DAPF CSFMNRs was assessed, and comparable adsorption capacities (83.3 mg g(-1)) to the largest value were demonstrated. A thermodynamic study of the adsorption clearly indicated that the adsorption was exothermic and spontaneous. Due to the ferromagnetic properties with a high saturation magnetization value (56.1 emu g(-1)) of the nanorods, the nanorods exhibited excellent reusability with one of the fastest recovery times (25 s) among reported materials. Therefore, the Fe3O4@DAPF CSFMNRs can serve as recyclable adsorbent materials and as an alternative to commonly used sorbent materials for the rapid removal of heavy metals from aqueous solutions.

  3. Composites of nanotubular polyaniline containing Fe3O4 nanoparticles

    Institute of Scientific and Technical Information of China (English)

    龙云泽; 陈兆甲; 刘振兴; 张志明; 万梅香; 王楠林

    2003-01-01

    Results of charge-transport and magnetic measurements of nanotubular polyaniline (PANI) composites containing Fe3O4 nanoparticles (~10nm) synthesized by a "template-free" method are reported. The T-1/2 resistivity has been observed, and dc magnetic susceptibility data are fitted to an equation X = X* p + C/T. With increasing weight ratio of Fe3O4, the electrical conductivity and temperature-independent susceptibility X* p increase, and the Curietype susceptibility is suppressed at low temperatures. Further discussions have been given. The PANI-H3PO4/Fe3O4composite containing 27wt% of Fe3O4 nanoparticles is superparamagnetic, exhibiting very little hysteresis even at 5K.

  4. Composites of nanotubular polyaniline containing Fe3O4 nanoparticles

    Institute of Scientific and Technical Information of China (English)

    LongYun-Ze; ChenZhao-Jia; LiuZhen-Xing; ZhangZhi-Ming; WanMei-Xiang; WangNan-Lin

    2003-01-01

    Results of charge-transport and magnetic measurements of nanotubular polyaniline (PANI) composites containing Fe3O4 nanoparticles (-10nm) synthesized by a “template-free” method are reported. The T-1/2 resistivity has been observed, and dc magnetic susceptibility data are fitted to an equation χ=χP*+C/T. With increasing weight ratio of Fe3O4, the electrical conductivity and temperature-independent susceptibility χP* increase, and the Curietype susceptibility is suppressed at low temperatures. Further discussions have been given. The PANI-H3PO4/Fe3O4 composite containing 27wt% of Fe3O4 nanoparticles is superparamagnetic, exhibiting very little hysteresis even at 5K.

  5. Shape Memory Polymer Composites of Poly(styrene-b-butadiene-b-styrene Copolymer/Liner Low Density Polyethylene/Fe3O4 Nanoparticles for Remote Activation

    Directory of Open Access Journals (Sweden)

    Yongkun Wang

    2016-11-01

    Full Text Available Magnetically sensitive shape memory poly(styrene-b-butadiene-b-styrene copolymer (SBS/liner low density polyethylene (LLDPE composites filled with various contents of Fe3O4 nanoparticles were prepared. The influence of the Fe3O4 nanoparticles content on the thermal properties, mechanical properties, fracture morphology, magnetic behavior, and shape memory effect of SBS/LLDPE/Fe3O4 composites was systematically studied in this paper. The results indicated that homogeneously dispersed Fe3O4 nanoparticles ensured the uniform heat generation and transfer in the alternating magnetic field, and endowed the SBS/LLDPE/Fe3O4 composites with an excellent magnetically responsive shape memory effect. When the shape memory composites were in the alternating magnetic field (f = 60 kHz, H = 21.21 kA·m−1, the best shape recovery ratio reached 99%, the shape retention ratio reached 99.4%, and the shape recovery speed increased significantly with the increment of Fe3O4 nanoparticles. It is anticipated that tagging products with this novel shape memory composite is helpful for the purpose of an intravascular delivery system in Micro-Electro-Mechanical System (MEMS devices.

  6. Synthesis and characterization of new functionalized polymer-Fe3O4 nanocomposite particles

    Directory of Open Access Journals (Sweden)

    A. Bukowska

    2017-01-01

    Full Text Available In this study, Fe3O4 nanoparticles (NPs were functionalized with copolymer or terpolymer bearing glycidyl methacrylate (GMA moieties making them suitable for potential applications as drug delivery systems (DDS. For this purpose, the surface of magnetic nanoparticles was first coated with 3-(trimethoxysilyl propyl methacrylate (MPS by a silanization reaction to introduce reactive methacrylate groups onto the surface. Subsequently, monomers were grafted onto the surface of modified-MPS particles via two polymerization methods: seed emulsion (GMA, divinylbenzene, DVB, and styrene, S and distillation – precipitation (GMA and DVB. The obtained nanocomposite particles were characterized by FTIR (Fourier transform infrared spectroscopy, DR UV-Vis (diffuse reflectance ultraviolet – visible spectroscopy, TEM (transmission electron microscopy combined with EDS (energy dispersive X-ray spectroscopy analysis and DLS (dynamic light scattering. FTIR spectroscopy showed that indeed a polymerFe3O4@MPS composite was obtained. TEM and EDS analysis showed that the seed emulsion method resulted in nanosized, 100 nm Fe3O4@MPS core/polymer shell NPs, forming long chains. On the contrary, the distillation – precipitation method caused the formation of an inverted structure, i.e. polymer core coated by a Fe3O4@MPS shell, which exhibited a very coarse size distribution varying from several hundreds to over 2 µm.

  7. Properties of poly(1-naphthylamine)/Fe3O4 composites and arsenic adsorption capacity in wastewater

    Science.gov (United States)

    Tran, Minh Thi; Nguyen, Thi Huyen Trang; Vu, Quoc Trung; Nguyen, Minh Vuong

    2016-03-01

    The research results of poly(1-naphthylamine)/Fe3O4 (PNA/Fe3O4) nanocomposites synthesized by a chemical method for As(III) wastewater treatment are presented in this paper. XRD patterns and TEM images showed that the Fe3O4 grain size varied from 13 to 20 nm. The results of Raman spectral analysis showed that PNA participated in part of the PNA/Fe3O4 composite samples. The grain size of PNA/Fe3O4 composite samples is about 25-30 nm measured by SEM. The results of vibrating sample magnetometer measurements at room temperature showed that the saturation magnetic moment of PNA/Fe3O4 samples decreased from 63.13 to 43.43 emu/g, while the PNA concentration increased from 5% to 15%. The nitrogen adsorption-desorption isotherm of samples at 77 K at a relative pressure P/ P 0 of about 1 was studied in order to investigate the surface and porous structure of nanoparticles by the BET method. Although the saturation magnetic moments of samples decreased with the polymer concentration increase, the arsenic adsorption capacity of the PNA/Fe3O4 sample with the PNA concentration of 5% is better than that of Fe3O4 in a solution with pH = 7. In the solution with pH > 14, the arsenic adsorption of magnetic nanoparticles is insignificant.

  8. CHARACTERIZATION OF MANGANESE PHTHALOCYANINE-Fe3O4 NANOPARTICLE COMPOSITE AND ITS ELECTROMAGNETORHEOLOGICAL FLUID

    Institute of Scientific and Technical Information of China (English)

    1999-01-01

    Manganese phthalocyanine (MnPc)-Fe3O4 nanoparticles composite was prepared and characterized. The results show that MnPc are complexed on the surface of Fe3O4 nanoparticles in the state of single molecule. There is effective composite between MnPc and Fe3O4 nanoparticles which can improve the antioxidization ability of Fe3O4 nanoparticles greatly. The composite was dispersed into chlorinated paraffin oil to form electromagnetorheological (EMR) fluid with high activity,and the EMR properties of this EMR fluid are studied.

  9. Synthesis and Characterization of Composite UPR/Fe3O4 for Its Use as Electromagnetic Wave Absorber

    Science.gov (United States)

    Yusmaniar; Adi, W. A.; Taryana, Y.; Muzaki, R.

    2017-05-01

    Synthesis and characterization of UPR/Fe3O4 composite were performed to evaluate its potency as a electromagnet absorbent. The composite was prepared from the mixture of unsaturated polyester resin and magnetite powder of iron oxide. Fe3O4 was used as filler and unsaturated polyester resins (UPR) was used as a matrix. Fe3O4 magnetite was synthesized from iron objects using electro synthesis method. The raw material was blended in the beaker glass for 120 min and then pressed at temperature of 60 °C for 30 min. The composite is in a semi-crystalline form that consists of amorphous matrix and the various crystalline fillers. The functional group’s analysis of the composite showed that crosslink (bridges) was formed between the chains of individual polymer and between Fe3O4 magnetite filler and UPR matrix. The performance of microwave absorbent measured by VNA method showed the highest RL at the frequency of 10.44 GHz and 11.74 dB. This value was achieved with a composition of 10wt% Fe3O4 and 90wt% UPR. We concluded that the composite of UPR/Fe3O4 has been successfully demonstrated as an electromagnetic wave absorber.

  10. Study on the Properties of Metallophthalocyanine-Fe3O4 Nanoparticles Composite

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    The solubility,antioxidation ability,thermal stability,coercivity Hc and long term stability of MPc-Fe3O4-nanoparticles composite(M=Co,Cu,Ni,Mn) have been studied.The results show that MPc-Fe3O4 nanoparticles composite can be easily dissolved in dilute acid.The dissolving rate of different MPc-Fe3O4 nanoparticles composite is in the following order:M=Mn~M=Co<M=Cu<M=Ni.The antioxidation ability of Fe3O4 nanoparticles are improved greatly after their complex with MPc and there is good relationship between Toxidation of Fe3O4 nanoparticles and n ,the complex layers of MPc on the surface of the composite.The results also show that the thermal stability of Fe3O4 nanoparticles increases greatly and the Hc of them decreases dramatically after Fe3O4 nanoparticles form nanoscale composite with MPc.MPc-Fe3O4 nanoparticles composite have high long term stability.

  11. [Study on preparation of composite nano-scale Fe3O4 for phosphorus control].

    Science.gov (United States)

    Li, Lei; Pan, Gang; Chen, Hao

    2010-03-01

    Composite nano-scale Fe3O4 particles were prepared in sodium carboxymethyl cellulose (CMC) solution by the oxidation deposition method. The adsorptions of phosphorus by micro-scale Fe3O4 and composite nano-scale Fe3O4 were investigated in water and soil, and the role of cellulase in the adsorption of composite nano-scale Fe3O4 was studied. Kinetic tests indicated that the equilibrium adsorption capacity of phosphorous on the composite nano-scale Fe3O4 (2.1 mg/g) was less than that of micro-scale Fe3O4 (3.2 mg/g). When cellulase was added to the solution of composite nano-scale Fe3O4 to degrade CMC, the removal rate of P by the nanoparticles (86%) was enhanced to the same level as the microparticles (90%). In the column tests, when the composite nano-scale Fe3O4 suspension was introduced in the downflow mode through the soil column, 72% of Fe3O4 penetrated through the soil bed under gravity. In contrast, the micro-scale Fe3O4 failed to pass through the soil column. The retention rate of P was 45% in the soil column when treated by the CMC-stabilized nanoparticles, in comparison with only 30% for the untreated soil column, however it could be improved to 74% in the soil column when treated by both the CMC-stabilized nanoparticles and cellulase, which degraded CMC after the nanoparticles were delivered into the soil.

  12. Fe3O4/carbon coated silicon ternary hybrid composite as supercapacitor electrodes

    Science.gov (United States)

    Oh, Ilgeun; Kim, Myeongjin; Kim, Jooheon

    2015-02-01

    In this study, Fe3O4/carbon-coated Si ternary hybrid composites were fabricated. A carbon layer was directly formed on the surface of Si by the thermal vapor deposition. The carbon-coating layer not only prevented the contact between Si and reactive electrolyte but also provided anchoring sites for the deposition of Fe3O4. Fe3O4 nanoparticles were deposited on the surface of carbon-coated Si by the hydrazine reducing method. The morphology and structure of Fe3O4 and carbon layer were characterized via X-ray diffractometry, field emission scanning electron microscopy, field emission transmission electron microscopy, X-ray photoelectron spectroscopy, and thermogravimetric analyses. These characterizations indicate that a carbon layer was fully coated on the Si particles, and Fe3O4 particles were homogeneously deposited on the carbon-coated Si particles. The Fe3O4/carbon-coated Si electrode exhibited enhanced electrochemical performance, attributed to the high conductivity and stability of carbon layer and pseudocapacitive reaction of Fe3O4. The proposed ternary-hybrid composites may be potentially useful for the fabrication of high-performance electrodes.

  13. Rapid degradation of dyes in water by magnetic Fe(0)/Fe3O4/graphene composites.

    Science.gov (United States)

    Chong, Shan; Zhang, Guangming; Tian, Huifang; Zhao, He

    2016-06-01

    Magnetic Fe(0)/Fe3O4/graphene has been successfully synthesized by a one-step reduction method and investigated in rapid degradation of dyes in this work. The material was characterized by N2 sorption-desorption, scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), vibrating-sample magnetometer (VSM) measurements and X-ray photoelectron spectroscopy (XPS). The results indicated that Fe(0)/Fe3O4/graphene had a layered structure with Fe crystals highly dispersed in the interlayers of graphene, which could enhance the mass transfer process between Fe(0)/Fe3O4/graphene and pollutants. Fe(0)/Fe3O4/graphene exhibited ferromagnetism and could be easily separated and re-dispersed for reuse in water. Typical dyes, such as Methyl Orange, Methylene Blue and Crystal Violet, could be decolorized by Fe(0)/Fe3O4/graphene rapidly. After 20min, the decolorization efficiencies of methyl orange, methylene blue and crystal violet were 94.78%, 91.60% and 89.07%, respectively. The reaction mechanism of Fe(0)/Fe3O4/graphene with dyes mainly included adsorption and enhanced reduction by the composite. Thus, Fe(0)/Fe3O4/graphene prepared by the one-step reduction method has excellent performance in removal of dyes in water.

  14. The structure and properties of Fe3O4/P (NaUA-St-BA) magnetic composite nano particles

    Institute of Scientific and Technical Information of China (English)

    周春华; 张书香; 刘威; 王英姿; 杨鸿昌

    2004-01-01

    Fe3O4/P (NaUA-St-BA) core-shell composite micro spheres were in situ prepared by soapless polymerization of styrene and butyl acrylate, with Fe3O4magnetic colloidal particles coated with NaUA. The results of IR and XRD analysis demonstrated that the desired polymer chains have been covalently bonded to the surface of Fe3 O4 nano particles. The morphology analysis by TEM confirmed that the composite particles have the core-shell structure and a relatively uniform diameter of about 100nm. The magnetic properties of the obtained composite latex particles were measured by VSM and found that they exhibited super paramagnetic properties.Finally, the prepared magnetic composite particles latex is stable for several months.

  15. Three-dimensional Fe3O4-graphene macroscopic composites for arsenic and arsenate removal.

    Science.gov (United States)

    Guo, Liangqia; Ye, Peirong; Wang, Jing; Fu, Fengfu; Wu, Zujian

    2015-11-15

    3D graphene macroscopic gel synthesized via self-assembly of GO nanosheets under basic conditions at low temperature is modified with polydopamine and Fe3O4 nanoparticles. The modification of polydopamine can not only strengthen the 3D graphene-based macroscopic architecture but also enhance the loadage and binding ability of Fe3O4 nanoparticles. The synthesized 3D Fe3O4-graphene macroscopic composites are characterized by SEM, XRD, XPS, BET, Raman and magnetic property and used as a versatile adsorbent for sub-ppm concentration of As(III) and As(V) removal from aqueous solutions. The experimental results suggest that the synthesized 3D Fe3O4-graphene macroscopic composites are promising for treating low concentration of arsenic contaminated water. Copyright © 2015 Elsevier B.V. All rights reserved.

  16. Facile synthesis of monodisperse superparamagnetic Fe3O4/PMMA composite nanospheres with high magnetization

    Science.gov (United States)

    Lan, Fang; Liu, Ke-Xia; Jiang, Wen; Zeng, Xiao-Bo; Wu, Yao; Gu, Zhong-Wei

    2011-06-01

    Monodisperse superparamagnetic Fe3O4/polymethyl methacrylate (PMMA) composite nanospheres with high saturation magnetization were successfully prepared by a facile novel miniemulsion polymerization method. The ferrofluid, MMA monomer and surfactants were co-sonicated and emulsified to form stable miniemulsion for polymerization. The samples were characterized by DLS, TEM, FTIR, XRD, TGA and VSM. The diameter of the Fe3O4/PMMA composite nanospheres by DLS was close to 90 nm with corresponding polydispersity index (PDI) as small as 0.099, which indicated that the nanospheres have excellent homogeneity in aqueous medium. The TEM results implied that the Fe3O4/PMMA composite nanospheres had a perfect core-shell structure with about 3 nm thin PMMA shells, and the core was composed of many homogeneous and closely packed Fe3O4 nanoparticles. VSM and TGA showed that the Fe3O4/PMMA composite nanospheres with at least 65% high magnetite content were superparamagnetic, and the saturation magnetization was as high as around 39 emu g - 1 (total mass), which was only decreased by 17% compared with the initial bare Fe3O4 nanoparticles.

  17. PREPARATION,COMPLEX MECHANISM AND STRUCTURE MODEL OF METALLOPHTHALOC- YANINE-Fe3O4 NANOPARTICLES COMPOSITE

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    MPc-Fe3O4-nanoparticles composite(M=Co, Cu, Ni, Mn) have been prepared and the factors that influence their mean size have been studied. The mean size of the nanoparticles composite increase with the increase of complex temperature. The interaction of MPc with Fe3O4 nanoparticles has been studied. There are M-O covalent bonding and ionic bonding between MPc and Fe3O4 nanoparticles. The intensities of M-O bonding and ionic bonding are in vestigated .The complex mechanism of MPc with Fe3O4 nanoparticles have been studied. First, there are complex between MPc and all Fe3O4 nanoparticles. Then, Fe3O4 nanoparticles accumulate together to form the accumulators, MPc have the function of cohering Fe3O4 nanoparticles. A considerable number of MPc combine with Fe3O4 nanoparticles on the surface of the accumulators to form MPc-Fe3O4 nanoparticles composite. All the above proesses take place spontaneously. The structure model of MPc-Fe3O4 nanoparticles composite has also been investigated. Inside the MPc-Fe3O4 nanoparticles composite, Fe3O4 nanoparticles accumulate together without order, on the surface of the composite, MPc form molecular dispersion layer. The threshold of molecular dispersion layer are also investigated.

  18. Hydrothermal synthesis of magnetic Fe3O4/graphene composites with good electromagnetic microwave absorbing performances

    Science.gov (United States)

    Zhu, Lingyu; Zeng, Xiaojun; Li, Xiaopan; Yang, B.; Yu, Ronghai

    2017-03-01

    The Fe3O4 sub-microspheres have been embedded uniformly into the reduced graphene oxide (rGO) to form a new-type Fe3O4/rGO composites through a one-pot solvothermal method. The dielectric properties for these magnetic Fe3O4/rGO composites can be greatly tuned by their different rGO additions. A good impedance matching from the balanced dielectric and magnetic loss is achieved in the Fe3O4/rGO composites with 4 wt% rGO addition, which dominates their excellent microwave absorbing performances including the minimum reflection loss (RL) value of -45 dB at a frequency of 8.96 GHz with a sample thickness of 3.5 mm and an effective absorption bandwidth of 3.2 GHz (below -10 dB) superior to those of the most magnetic materials and carbon-based composites. The controlled Fe3O4/rGO composite structure also exhibits high chemical stability and low density, which shows great potential application in high-performance electromagnetic microwave-absorbing materials.

  19. Preparation and characterization of Fe3O4/Au composite particles

    Institute of Scientific and Technical Information of China (English)

    CUI; Yali; HUI; Wenli; WANG; Huirong; WANG; Lijun; CHEN; Ch

    2004-01-01

    Using Fe3O4 nano-particles as seeds, a new type of Fe3O4/Au composite particles with core/shell structure and diameter of about 170 nm was prepared by reduction of Au3+ with hydroxylamine in an aqueous solution. Particle size analyzer and transmission electron microscope were used to analyze the size distribution and microstructure of the particles in different conditions. The result showed that the magnetically responsive property and suspension stability of Fe3O4 seeds as well as reduction conditions of Au3+ to Au0 are the main factors which are crucial for obtaining a colloid of the Fe3O4/Au composite particles with uniform particle dispersion,excellent stability, homogeneity in particle sizes, and effective response to an external magnet in aqueous suspension solutions. UV-Vis analysis revealed that there is a characteristic peak of Fe3O4/Au fluid. For particles with d(0.5)=168 nm, the λmax is 625 nm.

  20. Synthesis and Characterization of the Graphene-Fe3O4 Hybrid Composite.

    Science.gov (United States)

    Myekhlai, Munkhshur; Lee, Taejin; Lee, Sinil; Kim, Junhyo; Kang, Donghoon; Noh, Jungpil; Huh, Sunchul; Chung, Hanshik; Jeong, Hyomin

    2015-03-01

    Graphene and iron oxide composites have attracted huge attention in the fields of nanoelectronics and nanodevices due to their superior magnetic and electric characteristics. However, their synthesis methods are composed of many steps and use toxic chemical reactants. Accordingly, in this study, a GN-Fe3O4 NP hybrid composite was prepared using an eco-friendly and facile method. Its morphological and structural characteristics were then investigated by scanning electron microscopy, transmission electron microscopy, X-ray diffractometer and UV-visible spectroscopy. The results indicated that the GN structures as well as Fe3O4 NPs were significantly associated with the composite of GN-Fe3O4 NPs.

  1. Removing Cd2+ by Composite Adsorbent Nano-Fe3O4/Bacterial Cellulose

    Institute of Scientific and Technical Information of China (English)

    LU Min; GUAN Xiao-hui; WEI De-zhou

    2011-01-01

    A new composite adsorbent,nano-Fe3O4/bacterial cellulose(BC),was prepared through blending method.The process of adsorbing Cd2+ including its isotherm and kinetics measured was studied.The results show that the adsorption efficiency is improved because of huge surface area and surface coordination of nano-Fe3O4 particles.Its adsorption capacity is 27.97 mg/g and the maximum of Cd2+ removal is 74%.The adsorption kinetics can be described by pseudo-second rate model and the adsorption equilibrium by Langmuir type.The superparamagnetism of nano-Fe3O4 particles can help to solve the difficult separation of single BC adsorbent and lead to the quick separation of composite adsorbent from the liquid if a magnetic field was applied.Cd2+ can be desorbed effectively by EDTA and HCl from the composite adsorbent,which can make it be reused.

  2. Composites Based on Core-Shell Structured HBCuPc@CNTs-Fe3O4 and Polyarylene Ether Nitriles with Excellent Dielectric and Mechanical Properties

    Science.gov (United States)

    Pu, Zejun; Zhong, Jiachun; Liu, Xiaobo

    2017-10-01

    Core-shell structured magnetic carbon nanotubes (CNTs-Fe3O4) coated with hyperbranched copper phthalocyanine (HBCuPc) (HBCuPc@CNTs-Fe3O4) hybrids were prepared by the solvent-thermal method. The results indicated that the HBCuPc molecules were decorated on the surface of CNTs-Fe3O4 through coordination behavior of phthalocyanines, and the CNTs-Fe3O4 core was completely coaxial wrapped by a functional intermediate HBCuPc shell. Then, polymer-based composites with a relatively high dielectric constant and low dielectric loss were fabricated by using core-shell structured HBCuPc@CNTs-Fe3O4 hybrids as fillers and polyarylene ether nitriles (PEN) as the polymer matrix. The cross-sectional scanning electron microscopy (SEM) images of composites showed that there is almost no agglomeration and internal delamination. In addition, the rheological analysis reveals that the core-shell structured HBCuPc@CNTs-Fe3O4 hybrids present better dispersion and stronger interface adhesion with the PEN matrix than CNTs-Fe3O4, thus resulting in significant improvement of the mechanical, thermal and dielectric properties of polymer-based composites.

  3. Healing of Early Stage Fatigue Damage in Ionomer/Fe3O4 Nanoparticle Composites

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    Wouter Post

    2016-12-01

    Full Text Available This work reports on the healing of early stage fatigue damage in ionomer/nano-particulate composites. A series of poly(ethylene-co-methacrylic acid zinc ionomer/Fe3O4 nanoparticle composites with varying amounts of ionic clusters were developed and subjected to different levels of fatigue loading. The initiated damage was healed upon localized inductive heating of the embedded nanoparticles by exposure of the particulate composite to an alternating magnetic field. It is here demonstrated that healing of this early stage damage in ionomer particulate composites occurs in two different steps. First, the deformation is restored by the free-shrinkage of the polymer at temperatures below the melt temperature. At these temperatures, the polymer network is recovered thereby resetting the fatigue induced strain hardening. Then, at temperatures above the melting point of the polymer phase, fatigue-induced microcracks are sealed, hereby preventing crack propagation upon further loading. It is shown that the thermally induced free-shrinkage of these polymers does not depend on the presence of ionic clusters, but that the ability to heal cracks by localized melting while maintaining sufficient mechanical integrity is reserved for ionomers that contain a sufficient amount of ionic clusters guaranteeing an acceptable level of mechanical stability during healing.

  4. Synthesis of porous Fe3O4 hollow microspheres/graphene oxide composite for Cr(vi) removal.

    Science.gov (United States)

    Liu, Mancheng; Wen, Tao; Wu, Xilin; Chen, Changlun; Hu, Jun; Li, Jie; Wang, Xiangke

    2013-10-01

    A composite of porous Fe3O4 hollow microspheres/graphene oxide (Fe3O4/GO) has been fabricated through a facile self-assembly approach. Driven by the mutual electrostatic interactions, the amine-functionalized Fe3O4 microspheres prepared by a hydrothermal method and then modified by 3-aminopropyltrimethoxysilane were decorated with negatively-charged GO sheets. The Fe3O4 microspheres were hollow with porous surfaces and the surfaces were successfully modified with the amine, which was confirmed by Fourier transform infrared spectroscopy. The specific saturation magnetization of Fe3O4/GO was 37.8 emu g(-1). The sorption performance of Fe3O4/GO for Cr(vi) was evaluated. The maximum sorption capacity for Cr(vi) on Fe3O4/GO was 32.33 mg g(-1), which was much higher than that of Fe3O4 microspheres. The GO sheets could not only prevent agglomeration of the Fe3O4 microspheres and enable a good dispersion of these oxide microspheres, but also substantially enhance the specific surface area of the composite. The Fe3O4/GO composite may be a promising sorption material for the separation and preconcentration of heavy metal ions from aqueous solutions in environmental pollution cleanup.

  5. Development of a new aluminium matrix composite reinforced with iron oxide (Fe3O4

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    E. Bayraktar

    2010-01-01

    Full Text Available Purpose: of this paper is to develop new aluminium matrix (intermetallic composites reinforced with iron oxide (Fe3O4 that will be used in aeronautical engineering or in electronic industry. Different parameters such as sintering time and temperature, reinforcement, compact pressure were evaluated. The final purpose of this project is going on to improve conductivity and magnetic permeability of this new composite.Design/methodology/approach: In this paper, a new alternative materials “aluminium–iron oxide (Fe3O4, naturally as the mineral magnetite powder composite” has been developed by using a microwave (in the laboratory scale sintering programme with various aspect ratios, that iron oxide (Fe3O4 particle sizes and aluminium powders together were prepared. This paper contains partially preliminary results of our going-on research project.Findings: Green density increased regularly depending on the compact pressure and percentage of the iron oxide (Fe3O4. Micro and macro porosity was not found due to very clean microwave sintering. Density after microwave sintering was higher than that of traditional sintering in an electrical oven.Research limitations/implications: This project is going on and magnetic permeability and conductivity of this composite will be improved.Practical implications: This composite is new and clean and thanks to the new microwave sintering basically will be used in aeronautical engineering. Microwave heating results in lower energy costs and decreased processing times for many industrial processes.Originality/value: Originality of this paper is to use a new reinforcement in the aluminium matrix composite; Fe3O4-iron oxide. A new method - microwave sintering- has been carried out on this composite.

  6. Removal of dyes from industrial wastewater by polyaniline nano-composite/ Fe3O4

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    Mehrdad Manteghiyan

    2016-12-01

    Full Text Available To supply healthy water and remove water contaminations are one of the serious concerns of modern societies. Various techniques and methods have been used to removecontaminants from industrial wastewater. The aim of this study was to remove yellow15 dye from industrial wastewater using nano-composite/Fe3O4. In this study, magnetic nanoparticles Fe3O4were synthesized firstly by chemical precipitation. Nanoparticles synthesis was confirmed by XRD and SEM techniques. Then, by polyanilinedeposition on nanoparticles, polyaniline nanocomposites were prepared and its synthesis was confirmed by TEM, SEM, and FTIR techniques. In addition, the effects of various parameters, including ph, contact time, adsorbent value, and temperature were investigated and optimized in the isolation of considered dye. Kinetics studies showed that the absorption kinetics follows a pseudo-second order equation and this dye adsorption isotherm follows a Langmuir Equation. The results showed that this method is an appropriate method for considered dye.

  7. Synthesis of BSA/Fe3O4 magnetic composite microspheres for adsorption of antibiotics.

    Science.gov (United States)

    Zhang, Baoliang; Zhang, Hepeng; Li, Xiangjie; Lei, Xingfeng; Li, Chunmei; Yin, Dezhong; Fan, Xinlong; Zhang, Qiuyu

    2013-10-01

    BSA/Fe3O4 magnetic composite microspheres with high saturation magnetization and paramagnetic property were prepared via inverse emulsion technology at room temperature, bovine serum albumin (BSA, 60 KD), magnetic nanoparticles (Fe3O4) and glutaraldehyde as macromonomer, inorganic particles and cross-linking agent, respectively. Fourier transform infrared (FTIR), scanning electron microscope (SEM), metalloscope, and particle size analyzer were used to characterize morphology and structure of composite microspheres. Vibrating sample magnetometer (VSM) and thermogravimetric analysis (TGA) were used to test magnetic properties of the synthesized samples, adsorption capacity of microspheres was determined by ultraviolet spectrophotometer (UV). The results showed that BSA/Fe3O4 microspheres were 43 μm with relatively narrow particle size distribution, perfect sphere-shaped morphologies, superparamagnetism with a saturation magnetization of 11 emu/g, and high magnetic content with a value of 57.29%. The main factors influencing properties of microspheres including raw material ratio, the amount of emulsifier and cross-linking agent, agitation speed were investigated and optimized. Furthermore, these microspheres accompanying with high separable and reusable efficient may have great potential application in the field of separation, in particular, removal of antibiotics. Adsorption capacities of the microspheres of four different kinds of antibiotics (erythromycin, streptomycin, tetracycline and chloramphenicol) ranging from 69.35 mg/g to 147.83 mg/g were obtained, and Langmuir isotherm model coincided with equilibrium data than that of the Freundlich model. © 2013 Elsevier B.V. All rights reserved.

  8. Microwave complex permeability of Fe3O4 nanoflake composites with and without magnetic field-induced rotational orientation

    Science.gov (United States)

    Liu, Xianguo; Wing Or, Siu; Ming Leung, Chung; Ho, S. L.

    2013-05-01

    Magnetite (Fe3O4) nanoflakes with widths of 100-200 nm and thicknesses of 10-80 nm were prepared by a hydrothermal synthesis method. Fe3O4 nanoflake composites with and without magnetic field-induced rotational orientation of flake planes of Fe3O4 nanoflakes in paraffin binder were fabricated using 35 wt. % Fe3O4 nanoflakes. The rotationally oriented composite showed higher permeability and resonance frequency than the nonoriented one, and its value of (μ0-1)fr reached 214.8 GHz and exceeded the Snoek's limit. Considering a uniform and a random distribution of flake planes of Fe3O4 nanoflakes in the oriented and nonoriented composites, respectively, the complex permeability of both composites was calculated using the Landau-Lifshitz-Gilbert equation and the Bruggeman's effective medium theory in the 2-18 GHz microwave frequency range.

  9. Preparation and properties of a nano TiO2/Fe3O4 composite superparamagnetic photocatalyst

    Institute of Scientific and Technical Information of China (English)

    LI Yuxiang; ZHANG Mei; GUO Min; WANG Xidong

    2009-01-01

    Nano TiO2/Fe3O4 composite particles with different molar ratios of TiO2 to Fe3O4 wefe prepared via sol-gel method. X-ray diffraction, transmission electron microscopy, and vibration sample magnetometry were used to characterize the TiO2/Fe3O4 particles. The photocatalytic activity of the particles was tested by degrading methyl blue solution under UV illumination (254 nm). The results indicate that with the con-tent of TiO2 increasing, the photocatalytic activity of the composite particles enhances, while the magnetism of the particles decreases. When the molar ratio of TiO2 to Fe3O4 is about 8, both the photocatalytic activity and magnetism of the TiO2/Fe3O4 particles are relatively high, and their photocatalytic activity remains well after repeated use.

  10. Synthesis and characterization of graphene oxide composite with Fe3O4

    Directory of Open Access Journals (Sweden)

    Chuanyu Sun

    2015-09-01

    Full Text Available In the paper, a magnetic composite of graphene oxide (MGO has been successfully synthesized through decomposition of iron (III acetylacetonate in the mixture solution of triethylene glycol and graphene oxide (GO. Atomic force microscopy (AFM, transmission electron microscopy (TEM, X-ray diffraction (XRD and superconducting quantum interference device were used to characterize the material. The results show that the magnetic Fe3O4 nanoparticles modified graphene oxide composite with superparamagnetic properties, and magnetization saturation of 16.4 emu/g has been obtained. The MGO has a good sustained-release performance, and in vitro cytotoxicity confirming its secure use as a potential drug carrier.

  11. One-step solvothermal synthesis of magnetic Fe3O4-graphite composite for Fenton-like degradation of levofloxacin.

    Science.gov (United States)

    Wang, Long; Zhao, Qi; Hou, Juan; Yan, Jin; Zhang, Fengshuang; Zhao, Jiahui; Ding, Hong; Li, Yi; Ding, Lan

    2016-01-01

    A novel Fe3O4-graphite composite was prepared, characterized, and investigated as a heterogeneous Fenton-like catalyst for the degradation of levofloxacin (LEV) in an aqueous solution. The results revealed that the Fe3O4-graphite composite exhibited excellent properties for the degradation and mineralization of LEV, achieving a nearly complete degradation of 50 mg L(-1) LEV in 15 min and 48% of total organic carbon removal in 60 min under optimal conditions. A large electronic conjugation structure exists in graphite, which may lead to the fast production of •OH radical species because of the easy reduction of Fe(III) to Fe(II). In addition, we observed that the graphite can degrade LEV in the presence of H2O2. Therefore, the synergistic results of the graphite structure and Fe3O4 magnetic nanoparticles (MNPs) may contribute to the high catalytic activity of the Fe3O4-graphite composite. Compared with pure Fe3O4 MNPs, lesser iron leaching of the Fe3O4-graphite composite was observed during the degradation of LEV. The degradation efficiency of LEV remained approximately 80% at the fifth recycling run, which indicates that the Fe3O4-graphite composite has potential applications in water treatment for removing organic pollutants.

  12. Removal of nitrate and phosphate using chitosan/Al2O3/Fe3O4 composite nanofibrous adsorbent: Comparison with chitosan/Al2O3/Fe3O4 beads.

    Science.gov (United States)

    Bozorgpour, Farahnaz; Ramandi, Hossein Fasih; Jafari, Pooya; Samadi, Saman; Yazd, Shabnam Sharif; Aliabadi, Majid

    2016-12-01

    In the present study the chitosan/Al2O3/Fe3O4 composite nanofibrous adsorbent was prepared by electrospinning process and its application for the removal of nitrate and phosphate were compared with chitosan/Al2O3/Fe3O4 composite bead adsorbent. The influence of Al2O3/Fe3O4 composite content, pH, contact time, nitrate and phosphate initial concentrations and temperature on the nitrate and phosphate sorption using synthesized bead and nanofibrous adsorbents was investigated in a single system. The reusability of chitosan/Al2O3/Fe3O4 composite beads and nanofibers after five sorption-desorption cycles were carried out. The Box-Behnken design was used to investigate the interaction effects of adsorbent dosage, nitrate and phosphate initial concentrations on the nitrate and phosphate removal efficiency. The pseudo-second-order kinetic model and known Freundlich and Langmuir isotherm models were used to describe the kinetic and equilibrium data of nitrate and phosphate sorption using chitosan/Al2O3/Fe3O4 composite beads and nanofibers. The influence of other anions including chloride, fluoride and sulphate on the sorption efficiency of nitrate and phosphate was examined. The obtained results revealed the higher potential of chitosan/Al2O3/Fe3O4 composite nanofibers for nitrate and phosphate compared with chitosan/Al2O3/Fe3O4 composite beads. Copyright © 2016 Elsevier B.V. All rights reserved.

  13. Interface composition between Fe3O4 nanoparticles and GaAs for spintronic applications

    Science.gov (United States)

    Hihath, Sahar; Kiehl, Richard A.; Benthem, Klaus van

    2014-08-01

    Recent interest in spintronic applications has necessitated the study of magnetic materials in contact with semiconductor substrates; importantly, the structure and composition of these interfaces can influence both device functionality and the magnetic properties. Nanoscale ferromagnet/semiconductor structures are of particular interest. In this study, the interface structure between a monolayer of ferromagnetic magnetite (Fe3O4) nanoparticles and a GaAs substrate was studied using cross-sectional transmission electron microscopy techniques. It was found that a continuous amorphous oxide interface layer separates the nanoparticles from the GaAs substrate, and that iron diffused into the interface layer forming a compositional gradient. Electron energy-loss near-edge fine structures of the O K absorption edge revealed that the amorphous oxide is composed of γ-Fe2O3 directly underneath the Fe3O4 nanoparticles, followed by a solid solution of Ga2O3 and FeO and mostly Ga2O3 when approaching the buckled oxide/substrate interface. Real-space density functional theory calculations of the dynamical form factor confirmed the experimental observations. The implication of the findings on the optimization of these structures for spin injection is discussed.

  14. Highly stable and magnetically separable alginate/Fe3O4 composite for the removal of strontium (Sr) from seawater.

    Science.gov (United States)

    Hong, Hye-Jin; Jeong, Hyeon Su; Kim, Byoung-Gyu; Hong, Jeongsik; Park, In-Su; Ryu, Taegong; Chung, Kang-Sup; Kim, Hyuncheol; Ryu, Jungho

    2016-12-01

    In this study, a highly stable alginate/Fe3O4 composite was synthesized, and systematically investigated for the practical application of strontium (Sr) removal in complex media, such as seawater and radioactive wastewater. To overcome the drawbacks of the use of alginate microspheres, high contents of alginic acid and Fe3O4 were used to provide a more rigid structure with little swelling and facile separation, respectively. The synthesized composite was optimized for particle sizes of alginate/Fe3O4 composite showed excellent Sr uptake (≈400.0 mg/g) and exhibited outstanding selectivity for Sr among various cations (Na, Mg, Ca and K). However, in diluted Sr condition (50 mg/L), Ca significantly affected Sr adsorption, resulting in a decrease of Kd value from 3.7 to 2.4 at the 0.01 M Ca. The alginate/Fe3O4 composite could be completely regenerated using 0.1 M HCl and CaCl2. In real seawater spiked with 50 mg/L of Sr, the alginate/Fe3O4 composite showed 12.5 mg/g of Sr uptake, despite the highly concentrated ions in seawater. The adsorption experiment for radio-active (90)Sr revealed a removal efficiency of 67% in real seawater, demonstrating the reliability of the alginate/Fe3O4 composite.

  15. Field-induced microwave absorption in Fe3O4 nanoparticles and Fe3O4/polyaniline composites synthesized by different methods

    Science.gov (United States)

    Kurlyandskaya, G. V.; Cunanan, Jessica; Bhagat, S. M.; Aphesteguy, J. C.; Jacobo, S. E.

    2007-08-01

    Three kinds of nanoscale powders containing Fe3O4 nanoparticles (NPs) have been studied by ferromagnetic resonance (FMR): (i) Fe3O4 NPs grown and then covered with polyaniline (PANI), (ii) unclad Fe3O4 NPs, and (iii) Fe3O4 NPs grown “in situ” with the PANI. In every case, there is no low field microwave absorption, rather a single FMR line is observed. However, the half-power widths are of order of 1 kOe presumably due to a distribution of internal fields. For type I particles with a low concentration (below 40%) of Fe3O4, the observed resonance fields (Hr) are close to those expected for spheres with negligible magnetocrystalline anisotropy. For all other cases, Hr values are significantly lower. Such shortfalls can be roughly understood by invoking dipolar interactions between the grains, stresses frozen in grains during manufacture (method III), as well as anisotropy fields when the specimens are prepared in an aligning field.

  16. One-step preparation of Fe3O4/Pd@polypyrrole composites with enhanced catalytic activity and stability.

    Science.gov (United States)

    Zhang, Hui; Liu, Yang; Wu, Jie; Xin, Baifu

    2016-08-15

    Core/shell Fe3O4/Pd@polypyrrole (PPy) composites with a Fe3O4 core and a PPy shell embedding Pd nanoparticles were prepared in one-step. The diameter of highly dispersed Pd nanoparticles was as small as 2.9nm owing to coordination interaction generated between Pd(2+) ions and amino groups on PPy chains. The outer PPy shell was only 6.8nm: on one hand, the coverage was beneficial to improving the stability of resulting composites; on the other hand, the shell was thin enough to permit free contact between embedding Pd nanoparticles and reactants. Additionally, the as-prepared Fe3O4/Pd@PPy composites displayed good magnetic separation property due to incorporation of Fe3O4 nanospheres. Based on above merits, they served as suitable catalyst candidates. Their catalytic performance and reusability were evaluated by reduction of 4-nitrophenol with sodium borohydride as reducing agent. Compared with traditional Fe3O4/Pd composites, Fe3O4/Pd@PPy composites not only showed superior catalytic activity; but also exhibited much better stability in successive cycling tests.

  17. Fe3O4/cyclodextrin polymer nanocomposites for selective heavy metals removal from industrial wastewater.

    Science.gov (United States)

    Badruddoza, Abu Zayed M; Shawon, Zayed Bin Zakir; Tay, Wei Jin Daniel; Hidajat, Kus; Uddin, Mohammad Shahab

    2013-01-02

    In this work, carboxymethyl-β-cyclodextrin (CM-β-CD) polymer modified Fe(3)O(4) nanoparticles (CDpoly-MNPs) was synthesized for selective removal of Pb(2+), Cd(2+), Ni(2+) ions from water. This magnetic adsorbent was characterized by TEM, FTIR, XPS and VSM. The adsorption of all studied metal ions onto CDpoly-MNPs was found to be dependent on pH, ionic strength, and temperature. Batch adsorption equilibrium was reached in 45 min and maximum uptakes for Pb(2+), Cd(2+) and Ni(2+) in non-competitive adsorption mode were 64.5, 27.7 and 13.2 mg g(-1), respectively at 25 °C. Adsorption data were fitted well to Langmuir isotherm and pseudo-second-order models for kinetic study. The polymer grafted on MNPs enhanced the adsorption capacity because of the complexing abilities of the multiple hydroxyl and carboxyl groups in polymer backbone with metal ions. In competitive adsorption experiments, CDpoly-MNPs could preferentially adsorb Pb(2+) ions with an affinity order of Pb(2+)>Cd(2+)>Ni(2+) which can be explained by hard and soft acids and bases (HASB) theory. Furthermore, we explored the recyclability of CDpoly-MNPs. Copyright © 2012 Elsevier Ltd. All rights reserved.

  18. A mild synthetic route to Fe3O4@TiO2-Au composites: preparation, characterization and photocatalytic activity

    Science.gov (United States)

    Ma, Jianqi; Guo, Shaobo; Guo, Xiaohua; Ge, Hongguang

    2015-10-01

    To prevent and avoid magnetic loss caused by magnetite core phase transitions involved in high-temperature crystallization of sol-gel TiO2, a direct and feasible low-temperature crystallization technique was developed to deposit anatase TiO2 nanoparticle shell on Fe3O4 sphere cores. To promote the photocatalytic efficiency of the obtained core-shell Fe3O4@TiO2 magnetic photocatalyst, uniformly distributed Au nanoparticles (NPs) were successfully immobilized on the core-shell Fe3O4@TiO2 spheres via a seed-mediated growth procedure. The 3 nm Au colloid absorbed on Fe3O4@TiO2 served as a nucleation site for the growth of Au NPs overlayer. The morphology, structure, composition and magnetism of the resulting composites were characterized, and their photocatalytic activities were also evaluated. In comparison to Fe3O4@TiO2, Fe3O4@TiO2-Au exhibited higher photocatalytic activity for organic degradation under UV irradiation. This enhanced mechanism may have resulted from efficient charge separation of photogenerated electrons and holes due to the Au NPs attached on the TiO2. In addition, the composites possessed superparamagnetic properties with a high saturation magnetization of 44.6 emu g-1 and could be easily separated and recycled by a magnet.

  19. Facile and straightforward synthesis of superparamagnetic reduced graphene oxide-Fe3O4 hybrid composite by a solvothermal reaction.

    Science.gov (United States)

    Liu, Yue-Wen; Guan, Meng-Xue; Feng, Lan; Deng, Shun-Liu; Bao, Jian-Feng; Xie, Su-Yuan; Chen, Zhong; Huang, Rong-Bin; Zheng, Lan-Sun

    2013-01-18

    A superparamagnetic reduced graphene oxide-Fe(3)O(4) hybrid composite (rGO-Fe(3)O(4)) was prepared via a facile and straightforward method through the solvothermal reaction of iron (III) acetylacetonate (Fe(acac)(3)) and graphene oxide (GO) in ethylenediamine (EDA) and water. By this method, chemical reduction of GO as well as the formation of Fe(3)O(4) nanoparticles (NPs) can be achieved in one step. The Fe(3)O(4) NPs are firmly deposited on the surfaces of rGO, avoiding their reassembly to graphite. The rGO sheets prevent the agglomeration of Fe(3)O(4) NPs and enable a uniform dispersion of these metal oxide particles. The size distribution and coverage density of Fe(3)O(4) NPs deposited on rGO can be controlled by varying the initial mass ratio of GO and iron precursor, Fe(acac)(3). With an initial mass ratio of GO and Fe(acac)(3) of 5:5, the surfaces of rGO sheets are densely covered by spherical Fe(3)O(4) NPs with an average size of 19.9 nm. The magnetic-functionalized rGO hybrid exhibits a good magnetic property and the specific saturation magnetization (M(s)) is 13.2 emu g(-1). The adsorption test of methylene blue from aqueous solution demonstrates the potential application of this rGO-Fe(3)O(4) hybrid composite in removing organic dyes from polluted water.

  20. Study on the impact of the dosages of nano-Fe3O4 on nano-Fe3O4/NR composites%纳米Fe3O4用量对纳米Fe3O4/NR复合材料性能影响的研究

    Institute of Scientific and Technical Information of China (English)

    韩海臻; 李光; 张可喜; 霍凯; 符新

    2011-01-01

    To adopt emulsion coagulating prepares nano-Fe3O4/NR compound, what Fe3O4 is to use chemistry to precipitate. The dosages of nano-Fe3O4 have the effect on mechanics function, thermal stability and processing function of nano-Fe3O4/NR compound. Results show that the dosages of nanoFe3O4 have apparent effect on the function of nano-Fe3O4/NR compound. Adding nano-Fe3O4 in the rubber, rubber compound's G' is higher, tan δ less, and the mechanics function and the thermal stability of nano-Fe3O4/NR compound have been raised. When nano-Fe3O4 dosages are 15%, the function of nano-Fe3O4/NR compound is fairly good.%采用乳液共凝法制备纳米Fe3O4/天然橡胶(NR)复合材料,所用纳米Fe3O4是用化学共沉淀法制备的纳米Fe3O4乳液.研究了纳米Fe3O4用量对纳米Fe3O4/NR复合材料的力学性能、热稳定性、加工性能的影响.结果表明:纳米Fe3O4的用量对纳米Fe3O4/NR复合材料的性能有较大的影响.在NR中加入纳米Fe3O4,混炼胶的G'较高,tan δ较小,提高了复合材料的力学性能和热稳定性.当纳米Fe3O4的质量分数为15%时,纳米Fe3O4 /NR复合材料的综合性能较好.

  1. Synthesis of Fe3O4@SiO2@polymer nanoparticles for controlled drug release

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    Novel multifunctional nanoparticles containing a magnetic Fe3O4@SiO2 sphere and a biocompatible block copolymer poly(ethylene glycol)-b-poly(aspartate)(PEG-b-PAsp) were prepared.The silica coated on the superparamagnetic core was able to achieve a magnetic dispersivity,as well as to protect Fe3O4 against oxidation and acid corrosion.The PAsp block was grafted to the surface of Fe3O4@SiO2 nanoparticles by amido bonds,and the PEG block formed the outermost shell.The anticancer agent doxorubicin(DOX) was loaded into the hybrid nanoparticles via an electrostatic interaction between DOX and PAsp.The release rate of DOX could be adjusted by the pH value.

  2. Synthesis and characterization of Fe3 O4/graphene composites%Fe3O4/石墨烯复合材料的制备与表征

    Institute of Scientific and Technical Information of China (English)

    罗俊; 王芳辉; 孔令汉; 张瑶; 朱红

    2015-01-01

    为了研究 Fe3 O 4形貌与其复合材料电磁吸收性能之间的关系,采用水热法制备了微粒和棒状两种形貌的 Fe3 O 4与石墨烯复合材料.利用 X 射线衍射(XRD)仪、透射电子显微镜(TEM)和矢量网络分析仪(VNA)对复合材料的结构、形貌以及电磁吸收性能进行了表征.结果表明,纳米 Fe3 O 4棒/石墨烯复合材料相比纳米 Fe3 O 4粒子/石墨烯具有更优异的电磁吸收性能,其在8~18 GHz 范围内小于-10 dB 频带宽9.8~17.9 GHz,说明材料的微波吸收性能和纳米粒子的形貌有关.%In order to study the relationship between the morphologies of Fe3 O 4 and the microwave absorption properties of its composites,Fe3 O 4 nanoparticles/graphene and Fe3 O 4 nanorod/graphene composites were pre-pared by hydrothermal method.The structure,morphology and microwave absorption properties of the com-posites were characterized by XRD,TEM and vector network analysis (VNA).The results indicated that the Fe3 O 4 nanorod/graphene composites had better microwave absorption ability than the Fe3 O 4 nanoparticles/gra-phene composites.The microwave absorption of Fe3 O 4 nanorod/graohene values less than -10 dB was in the ranges of 9.8-17.9 GHz,proving the microwave absorption performance greatly depends on the shape of nano-particles.

  3. Uniform Fe3O4-PANi/PS composite spheres with conductive and magnetic properties and their hollow spheres

    Science.gov (United States)

    Wang, Xiaocong; Tang, Saide; Liu, Jing; He, Ziqiong; An, Lijuan; Zhang, Chenxi; Hao, Jingmei; Feng, Wei

    2009-05-01

    Core-shell multifunctional composite spheres consisting of Fe3O4-polyaniline (PANi) shell and polystyrene (PS) core were fabricated using core-shell-structured sulfonated PS spheres (with uniform diameter of 250 nm) as templates. PANi was doped in situ by sulfonic acid resulting the composite spheres are well conductive. Dissolved with solvent, PS cores were removed from the core-shell composite spheres and hollow Fe3O4-PANi spheres were obtained. Removing the PANi and PS components by calcinations produced hollow Fe3O4 spheres. The cavity size of the hollow spheres was uniformly approximate to 190 nm and the shell thickness was 30 nm. The cavity size and the shell thickness can be synchronously controlled by varying the sulfonation time of the PS templates. The shell thickness in size range was of 20-86 nm when the sulfonation time was changed from 1 to 4 h. These resulting spheres could be arranged in order by self-assembly of the templates. Both the Fe3O4-PANi/PS composite spheres and the hollow Fe3O4 spheres exhibit a super-paramagnetic behavior. Scanning electron microscopy, transmission electron microscopy, Fourier transform infrared spectroscopy, and X-ray powder scattering were used to characterize these as-prepared spheres.

  4. A solvothermal method to produce RGO-Fe3O4 hybrid composite for fast chromium removal from aqueous solution

    Science.gov (United States)

    Zhou, Li; Deng, Huiping; Wan, Junli; Shi, Jun; Su, Tong

    2013-10-01

    A simple one step solvotermal strategy using non-toxic and cost-effective precursors has been developed to prepare reduced graphene oxide (RGO)-Fe3O4 non-nanocomposite for removal of Cr(VI). Compared with the nano-adsorbent, the RGO-Fe3O4 hybrid particles with size larger than 100 nm can reduce cell toxicity in water treatment processes. The structure, surface and magnetic characteristics of the non-nanocomposite were investigated by scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Brunauer-Emmett-Teller (BET), and Vibrating sample magnetometer (VSM). The RGO-Fe3O4 composite with the highest loading of Fe3O4 demonstrates the fastest removal of 500 μg/L Cr(VI) which can reach 85% within 5 min at neutral pH. The adsorption kinetics follows the pseudo-second-order model and the adosorbent exhibits better Cr(VI) removal efficiency in water at low pH. However, the removal efficiency of Cr(VI) decreased when common hazardous ions were added in water. The large saturation magnetization (41.12 emu/g) of the synthesized non-nanoparticles allows fast separation of the adsorbent from water. The RGO-Fe3O4 non-nanocomposite could be utilized as an efficient, stable, less toxic and magnetically separable adsorbent for environmental cleanup.

  5. Preparation and drug-loading properties of Fe3O4/Poly(styrene-co-acrylic acid) magnetic polymer nanocomposites

    Science.gov (United States)

    Lu, Wensheng; Shen, Yuhua; Xie, Anjian; Zhang, Weiqiang

    2013-11-01

    Fe3O4/poly(styrene-co-acrylic acid) magnetic polymer nanocomposites were synthesized by the dispersion polymerization method using styrene as hard monomer, acrylic acid as functional monomer, Fe3O4 nanoparticles modified with oleic acid as core, and poly(styrene-co-acrylic acid) as shell. Drug-loading properties of magnetic polymer nanocomposites with curcumin as a model drug were also studied. The results indicated that magnetic polymer nanocomposites with monodisperse were obtained, the particle size distribution was 50-120 nm, and the average size was about 100 nm. The contents of poly(styrene-co-acrylic acid) and Fe3O4 nanoparticles in magnetic polymer nanocomposites were 74% and 24.7%, respectively. The drug-loading capacity and entrapment efficiency were 2.5% and 44.4%, respectively. The saturation magnetization of magnetic polymer nanocomposites at 300 K was 20.2 emu/g without coercivity and remanence. The as-prepared magnetic polymer nanocomposites have not only lots of functional carboxyl groups but also stronger magnetic response, which might have potential applications in drug carrier and targeted drug release.

  6. Magnetic and microstructural properties of Fe3O4-coated Fe powder soft magnetic composites

    Science.gov (United States)

    Jo Sunday, Katie; Hanejko, Francis G.; Taheri, Mitra L.

    2017-02-01

    Soft magnetic composites (SMCs) comprised of ferrite-coated ferrous powder permit isotropic magnetic flux capabilities, lower core losses, and complex designs through the use of traditional powder metallurgy techniques. Current coating materials and methods are vastly limited by the nonmagnetic properties of organic and some inorganic coatings and their inability to withstand high heat treatments for proper stress relief of core powder after compaction. Ferrite-based coatings are ferrimagnetic, highly resistive, and possess high melting temperatures, thus providing adequate electrical barriers between metallic particles. In this work, iron powder was coated with Fe3O4 particles via mechanical milling, then compacted and cured in an inert gas environment. We find density and coercivity to improve with increasing temperatures; however, core loss greatly increases, which is attributed to the formation of a more conductive iron-oxide phase and less resistive Fe volume. Our work begins to exemplify the unique qualities and potential for ferrite-based coatings using traditional powder metallurgy techniques and higher curing temperatures for electromagnetic devices.

  7. Self-assembly and graft polymerization route to Monodispersed Fe3O4@SiO2--polyaniline core-shell composite nanoparticles: physical properties.

    Science.gov (United States)

    Reddy, Kakarla Raghava; Lee, Kwang-Pill; Kim, Ju Young; Lee, Youngil

    2008-11-01

    This study describes the synthesis of monodispersed core-shell composites of silica-modified magnetic nanoparticles and conducting polyaniline by self-assembly and graft polymerization. Magnetic ferrite nanoparticles (Fe3O4) were prepared by coprecipitation of Fe+2 and Fe+3 ions in alkaline solution, and then silananized. The silanation of magnetic particles (Fe3O4@SiO2) was carried out using 3-bromopropyltrichlorosilane (BPTS) as the coupling agent. FT-IR spectra indicated the presence of Fe--O--Si chemical bonds in Fe3O4@SiO2. Core-shell type nanocomposites (Fe3O4@SiO2/PANI) were prepared by grafting polyaniline (PANI) on the surface of silanized magnetic particles through surface initiated in-situ chemical oxidative graft polymerization. The nanocomposites were characterized by high resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), X-ray photoelectron spectra (XPS), Fourier transform infrared (FTIR) spectra, UV-visible spectroscopy, photoluminescence (PL) spectra, electrical conductivity and magnetic characteristics. HRTEM images of the nanocomposites revealed that the silica-modified magnetic particles made up the core while PANI made up the shell. The XPS spectrum revealed the presence of silica in the composites, and the XRD results showed that the composites were more crystalline than pure PANI. PL spectra show that composites exhibit photoluminescent property. Conductivity of the composites (6.2 to 9.4 x 10(-2) S/cm) was higher than that of pristine PANI (3.7 x 10(-3) S/cm). The nanocomposites exhibited superparamagnetism. Formation mechanism of the core-shell structured nanocomposites and the effect of modified magnetic nanoparticles on the electro-magnetic properties of the Fe3O4@SiO2/PANI nanocomposites are also investigated. This method provides a new strategy for the generation of multi-functional nanocomposites that composed of other conducting polymers and metal nanoparticles.

  8. Chemical synthesis of Fe/Fe3O4 core-shell composites with enhanced soft magnetic performances

    Science.gov (United States)

    Yang, Bai; Li, Xiaopan; Yang, Xueying; Yu, Ronghai

    2017-04-01

    The large-grain Fe/Fe3O4 composite particles with average size of about 1.2 μm have been fabricated by a facile one-step solvothermal method. The formation of high-purity Fe3O4 as the shells (90.14 wt%) and α-Fe as the cores (9.86 wt%) in the Fe/Fe3O4 composites leads to their high saturation magnetization of 119.6 A m2 Kg-1. Very low coercivity of 30 Oe is obtained in the composites due to their uniform cubic-shaped morphologies. Compared with Fe-based nanosized particles, these micron-sized magnetic Fe/Fe3O4 composites exhibit high air stability and good compactibility with high compressed density of 5.9 g cm-3. The fully compacted sample shows good soft magnetic properties including high magnetic induction B1.2k (H=1200 A/m) of 540 mT and good frequency-dependent magnetic properties with operating frequency up to 50 MHz superior to those of the most traditional soft magnetic ferrites, which promotes their potential applications in high-frequency and high-power magnetic devices.

  9. Magnetic recoverable Fe3O4-TiO2:Eu composite nanoparticles with enhanced photocatalytic activity

    Science.gov (United States)

    Stefan, M.; Leostean, C.; Pana, O.; Toloman, D.; Popa, A.; Perhaita, I.; Senilă, M.; Marincas, O.; Barbu-Tudoran, L.

    2016-12-01

    This work refers to the influence of Eu doping on the morphologic, structural and compositional properties of magnetic separable Fe3O4-TiO2 composite nanoparticles with photocatalytic activity. In this respect, Fe3O4-TiO2:Eu nanocomposites were prepared by seed mediated growth of TiO2:Eu through a sol-gel method onto preformed magnetite resulted from co-precipitation method. Different Eu concentration precursors were used for doping. The thermal behavior and the conversion of precursors into corresponding Fe3O4-TiO2:Eu composite nanoparticles were evidenced by FT-IR spectra and thermal analysis. The XRD, XPS and HRTEM investigations results indicate that nanocomposites contain besides Fe3O4-TiO2:Eu some amounts of iron titanate. Formation of FeTiO3 is suppressed by the increase of Eu doping level. Magnetic studies also indicated that nanocomposite exhibit superparamagnetic behavior at room temperature. The large surface area and mesoporous structure of magnetic nanocomposite were confirmed by the surface area (BET) and porosity measurements. It was demonstrated that the composite nanoparticles exhibit good photocatalytic activity toward the degradation of RhB solution and they can be used as efficient and conveniently recoverable photocatalyst.

  10. Facile preparation of magnetic mesoporous Fe3O4/C/Cu composites as high performance Fenton-like catalysts

    Science.gov (United States)

    Li, Keyan; Zhao, Yongqin; Janik, Michael J.; Song, Chunshan; Guo, Xinwen

    2017-02-01

    Fe-Cu composites with different compositions and morphologies were synthesized by a hydrothermal method combined with precursor thermal transformation. γ-Fe2O3/CuO and α-Fe2O3/CuO were obtained by calcining the Fe and Cu tartrates under air atmosphere at 350 °C and 500 °C, respectively, while Fe3O4/C/Cu was obtained by calcining the tartrate precursor under N2 atmosphere at 500 °C. The Fe3O4/C/Cu composite possessed mesoporous structure and large surface area up to 133 m2 g-1. The Fenton catalytic performance of Fe3O4/C/Cu composite was closely related to the Fe/Cu molar ratio, and only proper amounts of Fe and Cu exhibited a synergistic enhancement in Fenton catalytic activity. Cu inclusion reduced Fe3+ to Fe2+, which accelerated the Fe3+/Fe2+ cycles and favored H2O2 decomposition to produce more hydroxyl radicals for methylene blue (MB) oxidation. Due to the photo-reduction of Fe3+ and Cu2+, the Fenton catalytic performance was greatly improved when amending with visible light irradiation in the Fe3O4/C/Cu-H2O2 system, and MB (100 mg L-1) was nearly removed within 60 min. The Fe3O4/C/Cu composite showed good recyclability and could be conveniently separated by an applied magnetic field. Compared with conventional methods for mesoporous composite construction, the thermolysis method using mixed metal tartrates as precursors has the advantages of easy preparation and low cost. This strategy provides a facile, cheap and green method for the synthesis of mesoporous composites as excellent Fenton-like catalysts, without any additional reductants or organic surfactants.

  11. Synthesis and characterization of Fe3O4@SiO2 magnetic composite nanoparticles by a one-pot process

    Science.gov (United States)

    Zhang, Le; Shao, Hui-ping; Zheng, Hang; Lin, Tao; Guo, Zhi-meng

    2016-09-01

    Fe3O4@SiO2 core-shell composite nanoparticles were successfully prepared by a one-pot process. Tetraethyl-orthosilicate was used as a surfactant to synthesize Fe3O4@SiO2 core-shell structures from prepared Fe3O4 nanoparticles. The properties of the Fe3O4 and Fe3O4@SiO2 composite nanoparticles were studied by X-ray diffraction, transmission electron microscopy, energy dispersive spectroscopy, and Fourier transform infrared spectroscopy. The prepared Fe3O4 particles were approximately 12 nm in size, and the thickness of the SiO2 coating was approximately 4 nm. The magnetic properties were studied by vibrating sample magnetometry. The results show that the maximum saturation magnetization of the Fe3O4@SiO2 powder (34.85 A·m2·kg-1) was markedly lower than that of the Fe3O4 powder (79.55 A·m2·kg-1), which demonstrates that Fe3O4 was successfully wrapped by SiO2. The Fe3O4@SiO2 composite nanoparticles have broad prospects in biomedical applications; thus, our next study will apply them in magnetic resonance imaging.

  12. Synthesis and characterization of Fe3O4/AuNPs magnetic composite nanoparticles%Fe3O4/AuNPs磁性复合粒子的制备与表征

    Institute of Scientific and Technical Information of China (English)

    代昭; 杨坤; 黄丹丹; 初园园

    2015-01-01

    通过溶剂热法合成了较大粒径的磁性Fe3O4纳米粒子,使用3-氨丙基三乙氧基硅烷(APTES)在乙醇/异丙醇体系中将其表面功能化一层氨基,随后将金纳米粒子(AuNPs)自组装于Fe3O4粒子表面,得到了Fe3O4/AuNPs纳米粒子;采用透射电子显微镜(TEM)、X-射线衍射(XRD)、振动样品磁强计(VSM)和紫外-可见光吸收光谱仪(UV-Vis)对复合粒子的形态、结构及性质进行表征。结果表明:所制备的Fe3O4磁纳米粒子粒径均一,平均粒径约为250 nm,形状几乎都呈球形,磁性Fe3O4/AuNPs复合粒子包覆均匀、具有良好的的分散性和磁化率,同时兼有磁性和金纳米粒子的特性。%Fe3O4 magnetic nanoparticles with large particle size were synthesized by a solvothermal method, and then modified by (3-aminopropyl)triethoxysilane (APTES) in the system of ethanol and isopropanol, which can functionalized the surface a layer of amino groups. Then, magnetic Fe3O4/Au nanoparticles were prepared by connecting gold nanoparticles under the condition of ultrasound. These composite particles have been characterized by transmission electron microscopy (TEM), X-ray powder diffraction (XRD), vibrating sample magnetometer(VSM) and ultraviolet-visible spectrophotometer (UV-Vis). The result shows that the prepared Fe3O4 nanoparticles have a uniform particle size and spherical shape, the average size is 250 nm. Fe3O4/Au composite particles coated evenly, have a good dispersibility and magnetic susceptibility, possess magnetism and characteristics of gold nanoparticles at the same time.

  13. Hybrid composites made of multiwalled carbon nanotubes functionalized with Fe3O4 nanoparticles for tissue engineering applications

    Science.gov (United States)

    Cunha, C.; Panseri, S.; Iannazzo, D.; Piperno, A.; Pistone, A.; Fazio, M.; Russo, A.; Marcacci, M.; Galvagno, S.

    2012-11-01

    A straightforward technique for functionalization of multiwalled carbon nanotubes (MWCNTs) with magnetite (Fe3O4) nanoparticles was developed. Iron oxide nanoparticles were deposited on MWCNT surfaces by a deposition-precipitation method using Fe3+/Fe2+ salts precursors in basic solution. The characterizations by HRTEM, XRD, SEM/EDX, AAS and TPR analyses confirmed the successful formation of magnetic iron oxide nanoparticles on the MWCNT surface. Fe3O4/MWCNT hybrid composites were analysed in vitro by incubation with mesenchymal stem cells for 1, 3 and 7 days, either in the presence or absence of a static magnetic field. Analysis of cell proliferation was performed by the MTT assay, quantification of cellular stress was performed by the Lactate Dehydrogenase assay and analysis of cell morphology was performed by actin immunofluorescence and scanning electron microscopy. Results demonstrate that the introduction of magnetite into the MWCNT structure increases biocompatibility of oxidized MWCNTs. In addition, the presence of a static magnetic field further increases Fe3O4/MWCNT influence on cell behaviour. These results demonstrate this novel Fe3O4/MWCNT hybrid composite has good potential for tissue engineering applications.

  14. Fabrication and application progress of magnetite Fe3O4/CNTs particles nano-composite%磁性纳米Fe3O4/CNTs复合微粒的制备及应用进展

    Institute of Scientific and Technical Information of China (English)

    赵纯颖; 张爱波; 栾静繁; 孙黎

    2011-01-01

    In this paper,many different chemical methods for preparing Fe3O4/CNTs nano-composite particles were reviewed, including co-precipitation method,hydrothermal method,solvothermal method and thermal decomposition method. Furthermore,the specific applications and the development trend of Fe3O4/CNTs nano-composite particles in biomedical field,electrochemical,catalysis,biosensor,microwave absorbing material,electronic devices and sewage treatment were introduced.%综述了磁性纳米Fe3O4/CNTs复合微粒的制备方法,包括化学共沉淀法、水热法、溶剂热法、热分解法等.介绍了磁性纳米Fe3O4/CNTs复合微粒在生物医学、电化学、催化、生物传感器、吸波材料、电子设备、污水处理等方面的应用以及发展前景.

  15. Characterization of Fe3O4/P(St-MPEO) Amphiphilic Magnetic Polymer Microspheres

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Amphiphilic magnetic microspheres consisting of styrene and poly(ethylene oxide) macromonomer(MPEO) were prepared by dispersion copolymerization in the presence of Fe3O4 magnetic fluid in an ethanol/water medium. The sizes of the magnetic microspheres and their distribution were characterized by means of scanning electron microscopy(SEM). The surface morphology and the average surface roughness of the microspheres were investigated by virtue of atomic force microscopy(AFM). It was found that the microspheres exhibit microscopic phase-separate and the mean square surface roughness of the microspheres increases with increasing MPEO used in the copolymerization. The amphiphilic magnetic microspheres containing 0.4-3.5 mg/g hydroxyl groups could be prepared from MPEO with different concentrations and styrene.

  16. [Preparation of molecularly imprinted polypyrrole/Fe3O4 composite material and its application in recognition of tryptophan enantiomers].

    Science.gov (United States)

    Chen, Zhidong; Shan, Xueling; Kong, Yong

    2012-04-01

    Ferrosoferric oxide (Fe(3)O(4)) magnetic material was first synthesized, and then the in-situ chemical polymerization of pyrrole was carried out on the surface of Fe(3)O(4) by using pyrole and L-tryptophan (L-Trp) as the functional monomer and templates, respectively. As a result, molecularly imprinted polypyrrole/Fe(3)O(4) composite material was obtained. This composite material was separated from the solution because of its magnetic property. Polypyrrole in the composite was overoxidized in 1 mol/L NaOH solution by applying a potential of 1.0 V, and thus L-Trp templates were de-deoped from the composite. Scanning electron microscopy (SEM), X-ray diffraction (XRD) and electrochemical methods were employed to characterize the composite. The solution containing L- or D-Trp was pumped through a porous ceramic tube packed with the composite, separately. High performance liquid chromatography (HPLC) was adopted for the detection of L- or D-Trp in the eluate, and the results indicated that the enrichment ability of the composite for L-Trp was almost 2 times that of D-Trp. Therefore, the electro-magnetic composite material has potential applications as chromatographic stationary phase for chiral recognition.

  17. PREPARATION AND PROPERTIES OF ULTRAFINE COMPOSITE POWDERS OF Fe3O4 AND Ni/MICA

    Institute of Scientific and Technical Information of China (English)

    Yucheng Wu; Jiaqin Liu; Rujun Xue; Guozhong Wang; Lide Zhang

    2005-01-01

    This paper presents the preparation of ultrafine powders of Fe3O4 and Ni by a chemical method, followed by mixing the prepared powders with mica and other ultrafine powders for synthesizing microwave absorption coatings.The microwave attenuation rate of the coatings was measured by the Microwave Network Analyzer in the frequency range of 8-12 GHz at room temperature. The results indicate that microwave could be absorbed by the coatings with an effectiveness strongly dependent on the powder sort and content and the coating thickness.

  18. The Influence of Nano-Fe3O4 on the Microstructure and Mechanical Properties of Cementitious Composites

    Science.gov (United States)

    Sikora, Pawel; Horszczaruk, Elzbieta; Cendrowski, Krzysztof; Mijowska, Ewa

    2016-04-01

    In the last decade, nanotechnology has been gathering a spectacular amount of attention in the field of building materials. The incorporation of nanosized particles in a small amount to the building materials can influence their properties significantly. And it can contribute to the creation of novel and sustainable structures. In this work, the effect of nano-Fe3O4 as an admixture (from 1 to 5 wt.% in mass of the cement) on the mechanical and microstructural properties of cementitious composites has been characterised. The study showed that Fe3O4 nanoparticles acted as a filler which improved the microstructure of a cementitious composite and reduced its total porosity, thus increasing the density of the composite. The presence of nanomagnetite did not affect the main hydration products and the rate of cement hydration. In addition, the samples containing nanomagnetite exhibited compressive strength improvement (up to 20 %). The study showed that 3 wt.% of nano-Fe3O4 in the cementitious composite was the optimal amount to improve both its mechanical and microstructural properties.

  19. Amphiphilic comblike polymers enhance the colloidal stability of Fe(3)O(4) nanoparticles.

    Science.gov (United States)

    Kim, Myeongjin; Jung, Jaeyeon; Lee, Jonghwan; Na, Kyunga; Park, Subeom; Hyun, Jinho

    2010-03-01

    Stable colloidal dispersions of magnetite (Fe(3)O(4)) nanoparticles (MNPs) were obtained with the inclusion of an amphiphilic comblike polyethylene glycol derivative (CL-PEG) as an amphiphilic polymeric surfactant. Both the size and morphology of the resulting CL-PEG-modified MNPs could be controlled and were characterized by transmission electron microscopy (TEM). The interaction between MNPs and CL-PEG was confirmed by the presence of characteristic infrared absorption peaks, and the colloidal stability of the nanoparticle dispersion in water was evaluated by long-term observation of the dispersion using UV-visible spectroscopy. SQUID measurements confirmed the magnetization of CL-PEG-modified MNPs. The zeta potential of the CL-PEG-modified MNPs showed a dramatic conversion from positive to negative in response to the pH of the surrounding aqueous medium due to the presence of carboxyl groups at the surface. These carboxyl groups can be used to functionalize the MNPs with biomolecules for biotechnological applications. However, regardless of surface electrostatics, the flexible, hydrophilic side chains of CL-PEG-modified MNPs prevented the approach of adjacent nanoparticles, thereby resisting aggregation and resulting in a stable aqueous colloid. The cytotoxicity of MNPs and CL-PEG-modified MNPs was evaluated by a MTT assay.

  20. Effect of nanographene platelets (NGP) surface area on organic dye adsorption using Fe3O4-NGP composites

    Science.gov (United States)

    Taufik, A.; Saleh, R.

    2016-11-01

    Fe3O4-NanoGraphene Platelets (NGP) composites with different surface area were successfully synthesized using sol gel method. The inverse cubic spinel structures as well as graphitic like structure from NGP were detected using X-Ray Diffraction (XRD) Measurement, while the ferromagnetic behavior for all samples were detected using Vibrating Sample Magnetometry (VSM) measurement. The vibrational mode for all samples were characterized using Fourier Transform Infrared Spectroscopy (FT-IR), and thermal stability for all samples were characterized using Thermogravimetric Analysis (TGA). The adsorption process were tested using methylene blue (MB) as a model of organic pollutant. The result showed that the higher NGP surface area could enhance the adsorption capacity of the samples. The kinetic model of adsorption shows that the adsorption process of Fe3O4-NGP materials followed the second order kinetic reaction. The reusability of adsorbent were also performed to analyze the stability of the adsorbent.

  1. Facile preparation of superparamagnetic Fe3O4/poly(St-co-MPS)/SiO2 composite particles with high magnetization by introduction of silanol groups.

    Science.gov (United States)

    Yan, Feng; Li, Jun; Fu, Rong; Lu, Ziyang; Yang, Wensheng

    2009-10-01

    Fe3O4/poly(St-co-MPS) particles were prepared by encapsulation of Fe3O4 nanoparticles into copolymers of styrene (St) and 3-trimethoxysilylpropylmethacrylate (MPS) (poly(St-co-MPS)) prepared by miniemulsion copolymerization. It is found that the structure of the Fe3O4/poly(St-co-MPS)/SiO2 composite particles prepared by direct silica deposition on surface of the Fe3O4/poly(St-co-MPS) particles is dependent on the volume fraction of MPS used in the copolymerization. It is identified that the surface of the Fe3O4/poly(St-co-MPS) particles becomes more negatively charged with increased volume fraction of MPS used in the copolymerization, attributed to the increased amount of the silanol groups on the particles surface. Introduction of silanol groups on the particle surface is effective to improve the dispersibility of the Fe3O4/poly(St-co-MPS) particles and their compatibility with silica, allowing the facile preparation of Fe3O4/poly(St-co-MPS)/SiO2 composite particles with defined core-shell structure. The as-prepared Fe3O4/poly(St-co-MPS)/SiO2 composite particles show high magnetization, for example, saturation magnetization of the particles with average size of 140 nm and 6 nm silica shell is as high as 45 emu/g at 300 K.

  2. 石墨烯/Fe3O4复合材料的制备及电磁波吸收性能%Synthesis of Graphene/Fe3O4 Composite Materials and Their Electromagnetic Wave Absorption Properties

    Institute of Scientific and Technical Information of China (English)

    李国显; 王涛; 薛海荣; 胡园园; 何建平

    2011-01-01

    For expanding the application field of grahene. Electromagnetic wave absorption performance of the magnetic functionalization graphene has been researched in this paper. Graphene/Fe3O4 nanoparticle composites are prepared by microwave irradiating the suspension of graphite oxide and Fe3O, in the presence of hydrazine hydrate. Transmission electron microscopy and X-ray diffraction are used to characterize the structure and the distribution condition of the composites. Vector network analyzer is used to measure the complex permittivity and complex permeability of the composites in the frequency range of 0.1-18. 0 GHz. The permittivity dispersion behaviors are explained based on the Cole-Cole model. The reflection loss curves are calculated using computer simulation technique. Calculation results from the complex permittivity and permeability show that when the mass ratio of graphene to Fe3O4 is 10:1. Reflection losses exceeding - 20 dB can be obtained in the frequency range of 6.5-8.7 GHz for absorber thicknesses of 2.0-2.5 mm. By changing the relative content of the Fe3 O4 nanoparticles, minimum reflection loss can be obtained at -49.7 dB. Strong absorption properties of the composites indicate its potentially application as electromagnetic wave absorption material.%为扩展石墨烯的应用领域,对磁性功能化石墨烯的电磁波吸收性能进行研究.在氧化石墨与Fe3 O4粒子的悬浮液中添加还原剂水合肼,微波辐照反应制备石墨烯/Fe3 O4复合物.采用X射线衍射、透射电镜等手段对材料的结构和Fe3 O4的分布状态进行了测试表征.采用矢量网络分析仪测定了材料在0.1~18.0 GHz频率范围内的复介电常数和复磁导率.利用Cole-Cole图解释了复合材料的介电特性.利用计算机模拟出不同厚度材料的电磁波衰减性能.结果表明,当石墨烯和Fe3 O4粒子以质量比10∶1复合得到的吸波剂材料的匹配厚度在2.0~2.5 mm变化时,反射损耗小于一20 d

  3. Fabrication of nano-Fe3O4 3D structure on carbon fibers as a microwave absorber and EMI shielding composite by modified EPD method

    Science.gov (United States)

    Gholampoor, Mahdi; Movassagh-Alanagh, Farid; Salimkhani, Hamed

    2017-02-01

    Recently, electromagnetic interference (EMI) shielding materials have absorbed a lot of attention due to a growing need for application in the area of electronic and wireless devices. In this study, a carbon-based EMI shielding composite was fabricated by electrophoretic deposition of Fe3O4 nano-particles on carbon fibers (CFs) as a 3D structure incorporated with an epoxy resin. Co-precipitation method was employed to synthesize Fe3O4 nano-particles. This as-synthesized Fe3O4 nano-powder was then successfully deposited on CFs using a modified multi-step electrophoretic deposition (EPD) method. The results of structural studies showed that the Fe3O4 nano-particles (25 nm) were successfully and uniformly deposited on CFs. The measured magnetic properties of as-synthesized Fe3O4 nano-powder and nano-Fe3O4/CFs composite showed that the saturation magnetization of bare Fe3O4 was decreased from Ms = 72.3 emu/g to Ms = 33.1 emu/g for nano-Fe3O4/CFs composite and also corecivity of Fe3O4 was increased from Hc = 4.9 Oe to Hc = 168 Oe for composite. The results of microwave absorption tests revealed that the reflection loss (RL) of an epoxy-based nano-Fe3O4/CFs composite are significantly influenced by layer thickness. The maximum RL value of -10.21 dB at 10.12 GHz with an effective absorption bandwidth about 2 GHz was obtained for the sample with the thickness of 2 mm. It also exhibited an EMI shielding performance of -23 dB for whole the frequency range of 8.2-12.4 GHz.

  4. 聚苯胺/Fe_3O_4空心微球复合材料的制备及表征%Preparation and Characterization of Polyaniline/Fe_3O_4 Magnetic Hollow Microsphere Composites

    Institute of Scientific and Technical Information of China (English)

    许缙; 傅毛生; 黄剑; 许龙飞; 张存龙; 梁美玲

    2012-01-01

    用乙二醇为溶剂,三氯化铁和尿素为起始反应试剂,通过一步溶剂热法制备Fe3O4空心微球,经十二烷基苯磺酸钠改性后,以磺基水杨酸为乳化剂和掺杂剂,过二硫酸钾为氧化剂,采用乳液聚合法制备聚苯胺/Fe3O4空心微球复合材料,并利用X射线衍射仪(XRD)、红外光谱(IR)、透射电子显微镜(TEM)和物理特性测试仪(PPMS)表征样品的结构、形貌和磁性能。结果表明:复合材料为形似花状的Fe3O4空心微球均匀镶嵌在丝带网状的聚苯胺中间所构成,复合材料表现良好的磁性。%Magnetite hollow microspheres were successfully synthesized by a solvothermal route,using ethylene glycol(EG) as reaction solvent and FeCl3·6H2O and urea as the starting materials,and it was modified by sodium dodecyl benzene sulfonate(SDBS).Polyaniline/Fe3O4 magnetic hollow microsphere composites was prepared by emulsion polymerization,using sulfosalicylic acid(SSA) as emulsifier and doping agent and potassium persulfate as oxidant.Phase structure,morphology and magnetic properties of its corresponding products were characterized by X-ray diffraction(XRD),Fourier transform infrared spectroscopy(FT-IR),high-resolution transmission electron microscopy(TEM),and physical property measurement system(PPMS).The results showed that the composite was composed of the network structure of ribbon-like polyaniline in which flower-like Fe3O4 hollow microspheres were uniformly embedded,and the composite had good magnetic property.

  5. Synthesis for Magnetic Mesoporous Fe3O4-SiO2 Composites and Heterogeneous Fenton Degradation of Methyl Blue

    Science.gov (United States)

    Xie, Huanling; Zhang, Tengyun

    2014-12-01

    In this work, we presented a facile, one-step preparation for magnetic mesoporous Fe3O4-SiO2 composites under closely neutral conditions by an evaporation-induced self-assembly (EISA) and adding 1,3,5-TMB as co-solvent approach. The resulting samples were characterized by X-ray diffraction, N2 adsorption measurement, FT-IR and SEM. Magnetic mesoporous composites and H2O2 form heterogeneous Fenton in order to removal methylene blue as the dye wastewater model object. The catalysts showed high catalytic activity and stability in the decolorization of methlye blue.

  6. Competitive fluorescence assay for specific recognition of atrazine by magnetic molecularly imprinted polymer based on Fe3O4-chitosan.

    Science.gov (United States)

    Liu, Guangyang; Li, Tengfei; Yang, Xin; She, Yongxin; Wang, Miao; Wang, Jing; Zhang, Min; Wang, Shanshan; Jin, Fen; Jin, Maojun; Shao, Hua; Jiang, Zejun; Yu, Hailong

    2016-02-10

    A novel fluorescence sensing strategy for determination of atrazine in tap water involving direct competition between atrazine and 5-(4,6-dichlorotriazinyl) aminofluorescein (5-DTAF), and which exploits magnetic molecularly imprinted polymer (MMIP), has been developed. The MMIP, based on Fe3O4-chitosan nanoparticles, was synthesized to recognize specific binding sites of atrazine. The recognition capability and selectivity of the MMIP for atrazine and other triazine herbicides was investigated. Under optimal conditions, the competitive reaction between 5-DTAF and atrazine was performed to permit quantitation. Fluorescence intensity changes at 515 nm was linearly related to the logarithm of the atrazine concentration for the range 2.32-185.4 μM. The detection limit for atrazine was 0.86μM (S/N=3) and recoveries were 77.6-115% in spiked tap water samples.

  7. Aligned Structures of Fe3O4 Nanoparticles in a Curable Polymer Carrier Induced by a Magnetic Field

    Institute of Scientific and Technical Information of China (English)

    FANG Wen-Xiao; HE Zhen-Hui; XU Xue-Qing; SHEN Hui

    2005-01-01

    @@ To understand the interaction in dipolar systems, it is necessary to investigate the structures formed by the interacting particles. We introduce a polymer acrylic resin carrier to fix the structures in the magnetic fluid(Fe3O4). An aligned structure is investigated, which is formed under a magnetic field, and fixed in the cured acrylic resin film by evaporating the solvent at room temperature. The aligned structure is confirmed with the help of optical microscopy and optical diffraction for the cured film. Furthermore, we find substructures by using a scanning electronic microscope. Based on the curable and observable structures, a platform can be developed for investigating the aligned structures and configurations dominant by dipolar interaction. This is also helpful for the development of magnetic devices with orderly aligned structures.

  8. Constructing magnetic polyaniline/metal hybrid nanostructures using polyaniline/Fe 3O 4 composite hollow spheres as supports

    Science.gov (United States)

    Kong, Lirong; Lu, Xiaofeng; Jin, E.; Jiang, Shan; Bian, Xiujie; Zhang, Wanjin; Wang, Ce

    2009-08-01

    Polyaniline (PANI)/Fe 3O 4 composite hollow spheres have been successfully synthesized in one step using sulfonated polystyrene (PS) spheres as templates. The magnetic PANI hollow spheres were used as supports for noble metal nanoparticles (NPs) such as Au and Pd. The morphology, composition and magnetic properties of the resulting products were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, inductively coupled plasma (ICP) atomic spectra and vibrating sample magnetometer. The catalytic activity of magnetic PANI/Au composite shells on the oxidation of dopamine was investigated by cyclic voltammetry. The obtained results provide our product with a practical application for the detection of dopamine. On the other hand, the catalytic activity of magnetic PANI/Pd composite shells on the reduction of 4-nitroaniline was investigated by spectroscopic methods and compared with Pd/C catalyst which was already widely used in industrial production.

  9. Enhanced Photocatalytic Removal of Uranium(VI) from Aqueous Solution by Magnetic TiO2/Fe3O4 and Its Graphene Composite.

    Science.gov (United States)

    Li, Zijie; Huang, Zhiwei; Guo, Wenlu; Wang, Lin; Zheng, Lirong; Chai, Zhifang; Shi, Weiqun

    2017-04-14

    The separation and recovery of uranium from radioactive wastewater is important from the standpoints of environmental protection and uranium reuse. In the present work, magnetically collectable TiO2/Fe3O4 and its graphene composites were fabricated and utilized for the photocatalytical removal of U(VI) from aqueous solutions. It was found that, under ultraviolet (UV) irradiation, the photoreactivity of TiO2/Fe3O4 for the reduction of U(VI) was 19.3 times higher than that of pure TiO2, which is strongly correlated with the Fe0 and additional Fe(II) generated from the reduction of Fe3O4 by TiO2 photoelectrons. The effects of initial uranium concentration, solution pH, ionic strength, the composition of wastewater, and organic pollutants on the U(VI) removal by TiO2/Fe3O4 were systematically investigated. The results demonstrated its excellent performance in the cleanup of uranium contamination. As graphene can efficiently attract the TiO2 photoelectrons and thus decrease their transfer to Fe3O4, the photodissolution of Fe3O4 in the TiO2/graphene/Fe3O4 composite can be largely alleviated compared to that of the TiO2/Fe3O4, rendering this ternary composite a much higher stability. In addition, scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray absorption near edge spectroscopy (XANES), and X-ray photoelectron spectroscopy (XPS) were used to explore the reaction mechanisms.

  10. Efficient use of Fe metal as an electron transfer agent in a heterogeneous Fenton system based on Fe0/Fe3O4 composites.

    Science.gov (United States)

    Moura, Flávia C C; Araujo, Maria Helena; Costa, Regina C C; Fabris, José D; Ardisson, José D; Macedo, Waldemar A A; Lago, Rochel M

    2005-08-01

    In this work a novel heterogeneous Fenton system based on Fe(0)/Fe3O4 composites is described. The composites with several Fe(0)/Fe3O4 ratios were prepared by two different methods, i.e. mechanical alloying of Fe(0) and Fe3O4 powders and controlled reduction of Fe3O4 with H2. Reaction studies and detailed Conversion Electron Mössbauer surface characterization of the composites Fe(0)/Fe3O4, Fe(0), Fe3O4, alpha-Fe2O3 and gamma-Fe2O3 suggested that Fe2+surf species are essential to produce an active Fenton system. Kinetic studies for the oxidation of the dye methylene blue, used as an organic model molecule, and for the peroxide decomposition suggest that the reactions proceed via HO* radicals generated from Fe2+surf species and H2O2 in a Fenton like mechanism. The increase in activity caused by the addition of Fe(0) is discussed in terms of a creation of Fe2+surf species during the preparation of the composite and by an electron transfer mechanism from Fe(0) to Fe3+surf during the Fenton reaction to regenerate the Fe2+surf active species.

  11. Removal of Chromium(VI from Aqueous Solutions Using Fe3O4 Magnetic Polymer Microspheres Functionalized with Amino Groups

    Directory of Open Access Journals (Sweden)

    Kai Wang

    2015-12-01

    Full Text Available Magnetic polymer microspheres (MPMs using glycidylmethacrylate (GMA as a functional monomer were synthesized in the presence of Fe3O4 nanoparticles via dispersion polymerization. After polymerization, the magnetic polymer microbeads were modified with ethylenediamine (EDA. The obtained ethylenediamine-functionalized magnetic microspheres (EDA-MPMs were characterized by scanning electron microscope (SEM, X-ray diffraction (XRD, vibrating-sample magnetometer (VSM and Fourier transform infrared (FT-IR spectroscopy. Then the EDA-MPMs were applied as adsorbents for the removal of Cr(VI from aqueous solution. Langmuir equation was appropriate to describe the experimental data. The maximum adsorption capacities obtained from the Langmuir model were 236.9, 242.1 and 253.2 mg/g at 298, 308 and 318 K, respectively. The Cr(VI adsorption equilibrium was established within 120 min and the adsorption kinetics was compatibly described by the pseudo-second order equation. The thermodynamic parameters (ΔG°, ΔH°, ΔS° of the sorption process revealed that the adsorption was spontaneous and was an endothermic process. The regeneration study demonstrated that the EDA-MPMs could be repeatedly utilized with no significant loss of adsorption efficiency.

  12. Speciation analysis of Mn(II)/Mn(VII) using Fe3O4@ionic liquids-β-cyclodextrin polymer magnetic solid phase extraction coupled with ICP-OES.

    Science.gov (United States)

    Chen, Songqing; Qin, Xingxiu; Gu, Weixi; Zhu, Xiashi

    2016-12-01

    Ionic liquids-β-cyclodextrin polymer (ILs-β-CDCP) was attached on Fe3O4 nanoparticles to prepare magnetic solid phase extraction agent (Fe3O4@ILs-β-CDCP). The properties and morphology of Fe3O4@ILs-β-CDCP were characterized by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction(XRD), size distribution and magnetic analysis. A new method of magnetic solid phase extraction (MSPE) coupled to ICP-OES for the speciation of Mn(II)/Mn(VII) in water samples was established. The results showed that Mn(VII) and total manganese [Mn(II)+Mn(VII)] were quantitatively extracted after adjusting aqueous sample solution to pH 6.0 and 10.0, respectively. Mn(II) was calculated by subtraction of Mn(VII) from total manganese. Fe3O4@ILs-β-CDCP showed a higher adsorption capacity toward Mn(II) and Mn(VII). Several factors, such as the pH value, extraction temperature and sample volume, were optimized to achieve the best extraction efficiency. Moreover, the adsorption ability of Fe3O4@ILs-β-CDCP would not be significantly lower after reusing of 10 times. The accuracy of the developed method was confirmed by analyzing certified reference materials (GSB 07-1189-2000), and by spiking spring water, city water and lake water samples. Copyright © 2016 Elsevier B.V. All rights reserved.

  13. Co-assembly of CdTe and Fe3O4 with molecularly imprinted polymer for recognition and separation of endocrine disrupting chemicals

    Science.gov (United States)

    Chang, Limin; Chen, Shaona; Chu, Jia; Li, Xin

    2013-11-01

    In this study, we present a general protocol to fabricate imprinting matrix co-loaded with CdTe quantum dots and Fe3O4 nanoparticles for the recognition of endocrine disrupting chemicals (EDCs). The resultant composites were characterized by transmission electron microscopy, fluorescence spectroscopy, and energy dispersive spectroscopy. The materials have been demonstrated to be characterized with spherical shape with a saturation magnetization value of 1.7 emu g-1. Furthermore, the rebinding experiments show that the resultant materials have greater affinity and selectivity towards p-nitrophenol (model EDCs) over structurally related compounds. We believe that the effective method proposed in this work might provide a platform to prepare magnetic and fluorescent molecularly imprinted polymers for the recognition and separation of EDCs.

  14. A novel adsorbent based on magnetic Fe3O4 contained polyvinyl alcohol/chitosan composite nanofibers for chromium (Ⅵ) removal

    Science.gov (United States)

    Yan, Eryun; Cao, Minglu; Jiang, Jinyu; Gao, Jianwei; Jiang, Congcheng; Ba, Xuewei; Yang, Xiuying; Zhang, Deqing

    2017-10-01

    The magnetic Fe3O4 contained polyvinyl alcohol/chitosan (Fe3O4@PVA/CS) composite nanofibers were successfully synthesized via the electrospinning method and characterized by scanning electron microscope (SEM), transmission electron microscope (TEM), vibrating sample magnetometer (VSM) and Fourier transform infrared (FT-IR). The composite nanofibers were used as a novel adsorbent for removing toxic chromium (Ⅵ) (CrⅥ) in aqueous solution. The doping of Fe3O4 nanoparticles (NPs) into the fibers had a positive effect on the absorption for CrⅥ ions both under neutral and acidic conditions, and the saturated adsorption reached the highest when pH was 3.0. The results of the kinetics of CrⅥ removal on the as-prepared Fe3O4@PVA/CS composite nanofibers suggested a rapid initial loading and a subsequent stable stage, and the adsorption was well described by the pseudo-first-order model. The possible CrⅥ removal mechanism of the magnetic Fe3O4@PVA/CS composite nanofibers was also proposed.

  15. Sub-micron-sized polyethylenimine-modified polystyrene/Fe3O4/chitosan magnetic composites for the efficient and recyclable adsorption of Cu(II) ions

    Science.gov (United States)

    Xiao, Changwei; Liu, Xijian; Mao, Shimin; Zhang, Lijuan; Lu, Jie

    2017-02-01

    A sub-micron-sized polyethylenimine(PEI)-modified polystyrene/Fe3O4/chitosan magnetic composite (PS/Fe3O4/CS-PEI) was developed as a novel adsorbent for the removal of Cu(II) ions from aqueous solutions. The PS/Fe3O4/CS-PEI microspheres with a diameter of ∼300 nm can be highly monodisperse and conveniently separated from suspensions by a magnet due to their excellent magnetism. When the PS/Fe3O4/CS-PEI microspheres were used as an absorbent for the absorption of Cu(II) ions, the adsorption isotherms and adsorption kinetics well fitted the Langmuir model and the pseudo-second-order model, respectively. The maximum adsorption capacity was about 204.6 mg g-1, which was higher than those of other chitosan adsorbents reported recently. The adsorption was considerably fast, reaching the equilibrium within 15 min. In addition, the adsorbed Cu(II) ions could be effectively desorbed using 0.1 mol L-1 NaOH solution, and the regeneration study proved that the composite microspheres could be repeatedly utilized without significant capacity loss after six cycles. All the results demonstrated that the synthesized sub-micron-sized magnetic PS/Fe3O4/CS-PEI composites can be used as an ideal adsorbent of Cu(II) ions for environmental cleanup applications.

  16. Graphene encapsulated Fe3O4 nanorods assembled into a mesoporous hybrid composite used as a high-performance lithium-ion battery anode material

    DEFF Research Database (Denmark)

    Huang, Wei; Xiao, Xinxin; Engelbrekt, Christian

    2017-01-01

    The discovery of new anode materials and engineering their fine structures are the core elements in the development of new-generation lithium ion batteries (LIBs). To this end, we herein report a novel nanostructured composite consisting of approximately 75% Fe3O4 nanorods and 25% reduced graphene...... oxide (rGO). Microscopy and spectroscopy analyses have identified that the Fe3O4 nanorods are wrapped (or encapsulated) by the rGO nanosheets via covalent bonding, which further self-assemble into a mesoporous hybrid composite networked by the graphene matrix. The composite has an average pore size...

  17. Fe3O4/PANI/P(MAA-co-NVP) multilayer composite microspheres with electric and magnetic features: assembly and characterization.

    Science.gov (United States)

    Luo, Yan-Ling; Fan, Li-Hua; Gao, Gai-Ling; Chen, Ya-Shao; Shao, Xiao-Hua

    2009-11-01

    A core-shell multilayered composite microsphere with electric and magnetic features was designed and prepared on the basis of mutilayered fabrication. This kind of microspheres was obtained by introducing a rod-like conductive polyanilline (PANI) or its derivatives onto the surface of magnetic Fe3O4 nanoparticles with 4,4'-diphenylmethane diisocyanate as a anchor molecule. Subsequently, the Fe3O4/PANI or Fe3O4/aniline oligomers microspheres, as a secondary core, were covered with a cross-linked shell layer which was constructed by a dispersion polymerization process of methacrylic acid and vinyl pyrrolidone. The structure and morphologies were characterized by using a FTIR, XRD, UV-vis, SEM, TEM and TGA. The average diameter of Fe3O4 nanoparticles prepared is about 10.7 nm, and the PANI nanobars hold the size in the range of about 20.4-25.6 nm. The PANI nanobars are covalently assembled on the surface of Fe3O4 nanoparticles mainly in a mode of extended or horizontal arrangements through XRD and TEM results. The electromagnetic properties were examined based on different polymerization degrees and component ratios of PANI or its derivatives, showing characteristics of soft magnetic materials and controllable conductivity. The multilayer microspheres can be readily used to perform separation and magnetism guide, even electric and pH-modulated drug release in the light of swelling determination and a laser diffraction particle size analyzer, and are potentially of interest for drug targeting purpose.

  18. Preparation of Fe3O4@Au nano-composites by self-assembly technique for immobilization of glucose oxidase

    Institute of Scientific and Technical Information of China (English)

    WANG XianXiang; HUANG Shuo; Shan Zhi; YANG WanSheni

    2009-01-01

    Superparamagnetism amination nanocrystals Fe3O4 with 3-aminopropyltriethyloxy silane (APTES) were prepared by modified co-precipitation method. Next, 4-5 nm gold nanoparticles, prepared by classical Frens procedure, were coated on the surface of the amination Fe3O4 by self-assembly technology. The prepared Fe3O4@Au nanocomposite particles were investigated by transmission electron microscopy (TEM), UV-vis, infrared spectrum (FT-IR), and vibrating sample magnetometer (VSM) in order to eluci-date the morphology, optics and magnetic properties of the nanocomposites. Their uniform distribution of particle size, which is about 15 nm, and good magnetic responsiveness were observed. In view of the fact that Fe3O4 owns superparamagnetism and that nano-gold can readily combine with biological molecules, glucose oxidase (GOx) was chosen as a model to penetrate the condition of immobilizing enzyme, and enzymatic properties of resultant immobilized enzyme were studied as well. By systematic optimization, we established that at 28℃, and pH (5.5) and when mole ratio of Fe3O4:HAuCl4 was 0.5:1, the immobilization provided the best results. Finally, we are glad to find that the immobilized enzyme exhibits excellent thermostability in addition to its better stability than free enzyme. Thus, herein de-scribed immobilized enzyme could be used repeatedly with the assistance of an external magnetic field.

  19. Thermal evaporation-induced anhydrous synthesis of Fe3O4-graphene composite with enhanced rate performance and cyclic stability for lithium ion batteries.

    Science.gov (United States)

    Dong, Yucheng; Ma, Ruguang; Hu, Mingjun; Cheng, Hua; Yang, Qingdan; Li, Yang Yang; Zapien, Juan Antonio

    2013-05-21

    We present a high-yield and low cost thermal evaporation-induced anhydrous strategy to prepare hybrid materials of Fe3O4 nanoparticles and graphene as an advanced anode for high-performance lithium ion batteries. The ~10-20 nm Fe3O4 nanoparticles are densely anchored on conducting graphene sheets and act as spacers to keep the adjacent sheets separated. The Fe3O4-graphene composite displays a superior battery performance with high retained capacity of 868 mA h g(-1) up to 100 cycles at a current density of 200 mA g(-1), and 539 mA h g(-1) up to 200 cycles when cycling at 1000 mA g(-1), high Coulombic efficiency (above 99% after 200 cycles), good rate capability, and excellent cyclic stability. The simple approach offers a promising route to prepare anode materials for practical fabrication of lithium ion batteries.

  20. Synthesis and Characterization of magnetic Fe3O4/Au Magnetic Composite Nanoparticles%Fe3O4/Au磁性纳米复合微粒的制备及表征

    Institute of Scientific and Technical Information of China (English)

    彭菊村; 吴波英; 陈杰

    2008-01-01

    实验中应用水相合成法制备Fe3O4/Au纳米复合微粒,通过对复合微粒生成过程的光谱检测,对生成物的磁响应性检测和采用HGMF磁分离,表明绝大多数颗粒既具有磁性,又具有纳米Au的特征.将获得的不同粒径的磁性颗粒分别与纯Fe3O4,Au纳米微粒进行选区电子衍射对比分析.结果表明,粒径越小的复合颗粒的衍射花样越接近纯Fe3O4,随粒径的增大,与纯Fe3O4的差异增大;当粒径增大到(15.8±2.8) nm,衍射花样与纯Au纳米颗粒的完全吻合,间接证实了Fe3O4/Au纳米复合微粒的核壳结构.

  1. Fe3O4/C composite with hollow spheres in porous 3D-nanostructure as anode material for the lithium-ion batteries

    Science.gov (United States)

    Yang, Zhao; Su, Danyang; Yang, Jinping; Wang, Jing

    2017-09-01

    3d transition-metal oxides, especially Fe3O4, as anode materials for the lithium-ion batteries have been attracting intensive attentions in recent years due to their high energy capacity and low toxicity. A new Fe3O4/C composite with hollow spheres in porous three-dimensional (3D) nanostructure, which was synthesized by a facile solvothermal method using FeCl3·6H2O and porous spongy carbon as raw materials. The specific surface area and microstructures of composite were characterized by nitrogen adsorption-desorption isotherm method, FE-SEM and HR-TEM. A homogeneous distribution of hollow Fe3O4 spheres (diameter ranges from 120 nm to 150 nm) in the spongy carbon (pore size > 200 nm) conductive 3D-network significantly reduced the lithium-ion diffusion length and increased the electrochemical reaction area, and further more enhanced the lithium ion battery performance, such as discharge capacity and cycle life. As an anode material for the lithium-ion battery, the title composite exhibit excellent electrochemical properties. The Fe3O4/C composite electrode achieved a relatively high reversible specific capacity of 1450.1 mA h g-1 in the first cycle at 100 mA g-1, and excellent rate capability (69% retention at 1000 mA g-1) with good cycle stability (only 10% loss after 100 cycles).

  2. Synthesis and drug-loading properties of folic acid-modified superparamagnetic Fe3O4 hollow microsphere core/mesoporous SiO2 shell composite particles

    Science.gov (United States)

    Yang, Yong; Guo, Xue; Wei, Kaiwei; Wang, Lijuan; Yang, Dandan; Lai, Lifang; Cheng, Meiling; Liu, Qi

    2014-01-01

    A drug delivery system, which not only has superparamagnetic property, higher surface area but also has targeting function, has been developed. The core/shell structural magnetic magnetite mesoporous silica microspheres with amine groups (Fe3O4-SiO2-NH2) were first fabricated by a one-pot direct co-condensation method, then folic acid-modified magnetic mesoporous silica composite microspheres (Fe3O4-SiO2-NHFA) were obtained by the bonding of the Fe3O4-SiO2-NH2 with folic acid as targeted molecule. The resultant composite microspheres were characterized by Fourier transform infrared spectroscopy, X-ray diffraction, transmission electron microscopy, scanning electron microscopy, low temperature nitrogen adsorption-desorption, and vibrating sample magnetometer. A well-known inflammational drug ibuprofen was used as a model drug to assess the loading and releasing behavior of the composite microspheres. Fe3O4-SiO2-NHFA system exhibits magnetic properties typical for superparamagnetic material with a higher saturation magnetization value of about 41.2 emu/g and has better capacity of drug storage (32.0 %) and sustained drug-release property. So this system has potential applications in biomedical field.

  3. Potential application of highly reactive Fe(0)/Fe3O4 composites for the reduction of Cr(VI) environmental contaminants.

    Science.gov (United States)

    Dos Santos Coelho, Flávia; Ardisson, José Domingos; Moura, Flávia C C; Lago, Rochel M; Murad, Enver; Fabris, José Domingos

    2008-03-01

    We describe the use of highly reactive Fe(0)/Fe3O4 composites for the reduction of Cr(VI) species in aqueous medium. The composites were prepared by simple mechanical alloying of metallic iron and magnetite in different proportions, i.e. Fe(0) 25, 50, 75 and 90wt%. While after 3h of reaction pure Fe(0) and pure Fe3O4 showed only a low reduction efficiency of 15% and 25% Cr(VI) conversion, respectively, the composites, in particular Fe(0)(25wt%)/Fe3O4, showed a remarkable activity with ca. 65% Cr(VI) conversion. Kinetic experiments showed a high reaction rate during the first 3h, which subsequently decreased strongly, probably due to a pH increase from 6 to 8. Experiments with composites based on Fe(0)/alpha-Fe2O3, Fe(0)/gamma-Fe2O3 and Fe(0)/FeOOH showed very low activities, suggesting that Fe(oct)2+ in the magnetite structure plays an important role in the reaction. Scanning and high resolution electron microscopies and Mössbauer spectra (transmission and conversion electron Mössbauer spectroscopy) indicated that the mechanical alloying process promotes a strong interaction and interface between the metallic and oxide phases, with the Fe(0) particles completely covered by Fe3O4 particles. The high efficiency of the composite Fe(0)/Fe3O4 for Cr(VI) reduction is discussed in terms of a special mechanism where an electron is transferred from Fe(0) to magnetite to reduce Fe(oct)3+ to Fe(oct)2+, which is active for Cr(VI) reduction.

  4. Degradation of p-Nitrophenol using magnetic Fe(0)/Fe3O4/Coke composite as a heterogeneous Fenton-like catalyst.

    Science.gov (United States)

    Wan, Dong; Li, Wenbing; Wang, Guanghua; Lu, Lulu; Wei, Xiaobi

    2017-01-01

    A Coke supported Fe3O4 and Fe(0) composite (Fe(0)/Fe3O4/Coke) was prepared for the first time with the aim of evaluating its ability to be used as heterogeneous catalyst for the Fenton degradation of p-Nitrophenol (p-NP). A four factor Box-Behnken design (BBD) coupled with response surface methodology (RSM) was applied to evaluate the effects of several operating parameters, namely Fe(0)/Fe3O4/Coke dosage, reaction temperature, initial pH and H2O2 concentration, on the removal efficiency of p-NP. A significant quadratic model (p-valuep-NP (100mg/L) conversion and 81% of COD removal were achieved after 120min of reaction time, respectively, under the optimum conditions, which agreed well with the modeling prediction. The recyclability of Fe(0)/Fe3O4/Coke was also investigated after three successive runs, in which p-NP degradation performances showed a slight difference with the first oxidation cycle with an acceptable iron leaching. Moreover, according to the main intermediate products identified by gas chromatography-mass spectrometry (GC-MS), a possible pathway of p-NP degradation was proposed based on hydrogen radicals ([H]) or hydroxyl radicals (•OH) mechanism.

  5. Monodisperse magnetite (Fe3O4) nanoparticles modified with water soluble polymers for the diagnosis of breast cancer by MRI method

    Science.gov (United States)

    Rezayan, Ali Hossein; Mousavi, Majid; Kheirjou, Somayyeh; Amoabediny, Ghasem; Ardestani, Mehdi Shafiee; Mohammadnejad, Javad

    2016-12-01

    In this study, magnetic nanoparticles (MNPs) were synthesized via co-precipitation method. To enhance the biocompatibility and colloidal stability of the synthesized nanoparticles, they were modified with carboxyl functionalized PEG via dopamine (DPA) linker. Both modified and unmodified Fe3O4 nanoparticles exhibited super paramagnetic behavior (particle size below 20 nm). The saturation magnetization (Ms) of PEGdiacid-modified Fe3O4 was 45 emu/g, which was less than the unmodified Fe3O4 nanoparticles (70 emu/g). This difference indicated that PEGdiacid polymer was immobilized on the surface of Fe3O4 nanoparticles successfully. To evaluate the efficiency of the resulting nanoparticles as contrast agents for magnetic resonance imaging (MRI), different concentration of MNPs and different value of echo time TE were investigated. The results showed that by increasing the concentration of the nanoparticles, transverse relaxation time (T2) decreased, which subsequently resulted in MR signal enhancement. T2-weighted MR images of the different concentration of MNPs in different value of echo time TE indicated that MR signal intensity increased with increase in TE value up to 66 and then remained constant. The cytotoxicity effect of the modified and unmodified nanoparticles was evaluated in three different concentrations (12, 60 and 312 mg l-1) on MDA-MB-231 cancer cells for 24 and 48 h. In both tested time (24 and 48 h) for all three samples, the modified nanoparticles had long life time than unmodified nanoparticles. Cellular uptake of modified MNPs was 80% and reduced to 9% by the unmodified MNPs.

  6. Adsorption of methylene blue using Fe3O4/CuO/ZnO/ nanographene platelets (NGP) composites with various NGP concentration

    Science.gov (United States)

    Tju, H.; Taufik, A.; Saleh, R.

    2016-11-01

    This study will examine the use of Fe3O4/CuO/ZnO nanocomposites that have been modified by Nanographene Platelets (NGP) as an adsorbent to degrade organic dye waste Methylene Blue (MB). The nanocomposites were synthesized using the sol-gel method then combined with three variatons of NGP weight percents by simple hydrothermal method. The Fe3O4/CuO/ZnO/NGP composites were characterized using the X-Ray Diffraction (XRD) spectroscopy, Fourier Transform Infrared (FTIR), Energy Dispersive X-Ray (EDX), Thermogravimetric Analysis (TGA) and Vibrating Sample Magnetometer (VSM). The composites exhibit ferromagnetic behaviour. The presence of hexagonal wurtzite of ZnO, monoclinic of CuO and cubic spinel of Fe3O4 were found in the composites. The graphitic-like structure represents the presence of the NGP in the composites. However, the addition of NGP weight percent reduces the thermal stability of the composites. The adsorption capability of the composites are analyzed by observing the degradation of organic dye Methylene Blue (MB) under dark condition. The NGP addition of 15 wt% show the best result of the composites to degrade Methylene Blue in alkaline condition. Adsorption mechanism of the composites with NGP addition tend to follow the model Langmuir adsorption kinetic models.

  7. High energy density asymmetric supercapacitor based on NiOOH/Ni3S2/3D graphene and Fe3O4/graphene composite electrodes.

    Science.gov (United States)

    Lin, Tsung-Wu; Dai, Chao-Shuan; Hung, Kuan-Chung

    2014-01-01

    The application of the composite of Ni3S2 nanoparticles and 3D graphene as a novel cathode material for supercapacitors is systematically investigated in this study. It is found that the electrode capacitance increases by up to 111% after the composite electrode is activated by the consecutive cyclic voltammetry scanning in 1 M KOH. Due to the synergistic effect, the capacitance and the diffusion coefficient of electrolyte ions of the activated composite electrode are ca. 3.7 and 6.5 times higher than those of the Ni3S2 electrode, respectively. Furthermore, the activated composite electrode exhibits an ultrahigh specific capacitance of 3296 F/g and great cycling stability at a current density of 16 A/g. To obtain the reasonable matching of cathode/anode electrodes, the composite of Fe(3)O(4) nanoparticles and chemically reduced graphene oxide (Fe(3)O(4)/rGO) is synthesized as the anode material. The Fe(3)O(4)/rGO electrode exhibits the specific capacitance of 661 F/g at 1 A/g and excellent rate capability. More importantly, an asymmetric supercapacitor fabricated by two different composite electrodes can be operated reversibly between 0 and 1.6 V and obtain a high specific capacitance of 233 F/g at 5 mV/s, which delivers a maximum energy density of 82.5 Wh/kg at a power density of 930 W/kg.

  8. Preparation and Properties of Fe_3O_4/Clinoptilolite Magnetic Composite%Fe_3O_4/斜发沸石磁性复合材料的制备及其性能

    Institute of Scientific and Technical Information of China (English)

    王维清; 冯启明; 董发勤; 李虎杰; 赵晓东

    2010-01-01

    采用化学共沉淀法制备Fe_3O_4磁流体,再与斜发沸石复合制备一系列不同Fe_3O_4载量的磁性斜发沸石,并进行X射线衍射(XRD)、扫描电子显微镜(SEM)、透射电子显微镜(TEM)、振动样品磁强计(VSM)等表征分析,测定了其磁分离回收率及Cu~(2+)、Zn~(2+)、Cd~(2+)的饱和交换吸附量.结果表明,Fe_3O_4微粒赋存于斜发沸石表面或相互聚集,磁性斜发沸石磁稳定性好,并具有良好的超顺磁性,其对Cu~(2+)、Zn~(2+)、Cd~(2+)的交换吸附性能与其所含斜发沸石相当,但随Fe_3O_4载量增加而降低.Fe_3O_4载量为25wt%时,其饱和磁化强度M_s、剩余磁化强度M_r分别为14.787和0.398A·m~2/kg,磁分离回收率为94.6%,Cu~(2+)、Zn~(2+)、Cd~(2+)的饱和交换吸附量分别为12.3、12.0和23.4mg/g.磁性斜发沸石经磁分离回收并放置于空气中100d后仍保持良好的超顺磁性和较高的磁分离回收率.

  9. RhB Adsorption Performance of Magnetic Adsorbent Fe3O4/RGO Composite and Its Regeneration through A Fenton-like Reaction

    Institute of Scientific and Technical Information of China (English)

    Yalin Qin; Mingce Long∗; Beihui Tan; Baoxue Zhou

    2014-01-01

    Adsorption is one of the most effective technologies in the treatment of colored matter containing wastewater. Graphene related composites display potential to be an effective adsorbent. However, the adsorp-tion mechanism and their regeneration approach are still demanding more efforts. An effective magnetically separable absorbent, Fe3O4 and reduced graphene oxide (RGO) composite has been prepared by an in situ coprecipitation and reduction method. According to the characterizations of TEM, XRD, XPS, Raman spectra and BET analyses, Fe3O4 nanoparticles in sizes of 10-20 nm are well dispersed over the RGO nanosheets, re-sulting in a highest specific area of 296.2 m2/g. The rhodamine B adsorption mechanism on the composites was investigated by the adsorption kinetics and isotherms. The isotherms are fitting better by Langmuir model, and the adsorption kinetic rates depend much on the chemical components of RGO. Compared to active carbon, the composite shows 3.7 times higher adsorption capacity and thirty times faster adsorption rates. Furthermore, with Fe3O4 nanoparticles as the in situ catalysts, the adsorption performance of composites can be restored by carrying out a Fenton-like reaction, which could be a promising regeneration way for the adsorbents in the organic pollutant removal of wastewater.

  10. Thermal decomposition assisted synthesis and upconversion property of Fe3O4@YPO4:Tm/Yb hybrid nano-composite phosphor

    Science.gov (United States)

    Tiwari, S. P.; Kumar, K.; Rai, V. K.

    2015-06-01

    Hybrid nano-composite phosphor has been successfully synthesized through thermal decomposition method. The dual phase of samples assigned by XRD analysis shows the formation of nano-composite with crystallite size 20 nm and 12 nm for YPO4: Tm/Yb and Fe3O4@YPO4:Tm/Yb respectively. The FESEM images show the spherical shape and non agglomerated formation of nanoparticles. Three bands in upconversion emission mode were found in intense blue at 472 nm, red at 662 nm and NIR at 798 nm regions corresponding to1G4 → 3H6, 1G4 → 3F4 and 3H4 → 3H6 transition states respectively. The lifetime for1G4 → 3H6 level is found 1150 microsecond and 1400 microsecond for YPO4: Tm/Yb and Fe3O4@YPO4:Tm/Yb samples respectively.

  11. Carbon-covered Fe3O4 hollow cubic hierarchical porous composite as the anode material for lithium-ion batteries

    Science.gov (United States)

    Chen, Shouhui; Zhou, Rihui; Chen, Yaqin; Fu, Yuanyuan; Li, Ping; Song, Yonghai; Wang, Li

    2017-04-01

    In this work, Prussian blue nanocrystals, a kind of cubic metal-organic frameworks, was firstly covered by a uniform layer of resorcinol-formaldehyde (RF) resin, and then followed with heat treatment at different pyrolysis temperatures. The effects of pyrolysis temperature on the morphologies, phase, pore size, and electrochemical performance of the pyrolysis products were studied in this work. The composite generated at 600 ∘C, FexC600, was a hollow cubic composite of Fe3O4 covered by a thin RF-derived carbon layer. The carbon layer on FexC600 was a robust and conductive protective layer, which can accommodate Fe3O4 NPs and withstand the huge volume change of Fe3O4 during the process of discharge and charge. When used as anodes for lithium-ion batteries, FexC600 showed excellent electrochemical performance. It delivered a discharge capacity of 1126 mAh g-1 with a coulombic efficiency of 98.8% at the current density of 100 mA g-1 after 100 times discharge/charge cycling. It even delivered a capacity of 492 mAh g-1 at the current density of 500 mA g-1. This cubic hollow composite would be a promising alternative anode material for lithium-ion batteries.

  12. A Novel Nanofilm Sensor Based on Poly-(Alizarin Red)/Fe3O4 Magnetic Nanoparticles-Multiwalled Carbon Nanotubes Composite Material for Determination of Nitrite.

    Science.gov (United States)

    Qu, Jianying; Dong, Ying; Yong, Wang; Lou, Tongfang; Du, Xueping; Qu, Jianhang

    2016-03-01

    Fe3O4 magnetic nanoparticles were synthesized by chemical co-precipitation with sodium citrate as surfactant and were characterized by FT-IR spectrometer, X-ray diffraction and transmission electron microscopy. A novel nitrite sensor was fabricated by electropolymerization of alizarin red on the surface of glassy carbon electrode modified with Fe3O4-multiwalled carbon nanotubes composite nanofilm. Under the optimal experimental conditions, it was showed that the proposed sensor exhibited good electrocatalytic activity to the oxidation of nitrite, and the peak current increased linearly with the nitrite concentration from 9.64 x 10(-6) mol x L(-1) to 1.30 x 10(-3) mol x L(-1) (R = 0.9976) with a detection limit of 1.19 x 10(-6) mol x L(-1) (S/N = 3). This sensor showed excellent sensitivity, wide linear range, stability and repeatability for nitrite determination with potential applications.

  13. Photo-, sono- and sonophotocatalytic degradation of methylene blue using Fe3O4/ZrO2 composites catalysts

    Science.gov (United States)

    Kristianto, Y.; Taufik, A.; Saleh, R.

    2017-07-01

    In the present work, magnetite material Fe3O4/ZrO2 with various molar ratios was prepared by the two-step method (sol-gel followed by the ultrasonic-assisted method). The as-prepared samples were fairly characterized by various characterization methods, such as X-ray Diffraction (XRD), Vibrating Sample Magnetometer (VSM), Fourier Transform Infrared (FT-IR) and Thermal Gravimetric Analysis (TGA). The catalytic performance of the as-prepared samples was evaluated based on the degradation of methylene blue under UV light, ultrasound and combination of UV and ultrasound irradiation. The results revealed that the sample with Fe3O4:ZrO2 molar ratio of 0.5:1 showed the best catalytic performance under UV, ultrasound and UV + ultrasound irradiation. The degradation of methylene blue follows the order: sonophotocatalytic > sonocatalytic > photocatalytic. In addition, the effect of various scavengers has also been studied. Furthermore, all prepared samples could be used as a convenient recyclable catalyst.

  14. Magnetic Fe3O4-graphene composites as targeted drug nanocarriers for pH-activated release

    Science.gov (United States)

    Fan, Xiujuan; Jiao, Guozheng; Zhao, Wei; Jin, Pengfei; Li, Xin

    2013-01-01

    A novel nanocarrier of magnetic Fe3O4-graphene nanocomposites (MGNs) was proposed as an effective drug delivery system for cancer treatment. The nanocarrier was synthesized by covalently attaching modified Fe3O4 nanoparticles onto water-soluble graphene sheets via the formation of an amide bond with the aid of 1-ethyl-3-(3-dimethyaminopropyl) carbodiimide. The obtained MGNs exhibited excellent dispersibility and stability in aqueous solution and they also exhibited superparamagnetic properties with a saturation magnetization of 23.096 emu g-1. An efficient loading of 5-fluorouracil (5-FU) on MGNs as high as 0.35 mg mg-1 was obtained. Furthermore, the in vitro drug release of 5-FU was examined in pH 6.9 and pH 4.0 buffers at 37 °C, and showed strong pH dependence. Transmission electron microscope observations revealed that MGNs can be internalized efficiently by HepG2 cells. More importantly, the cytotoxicity evaluation shows that the resulting MGNs exhibit excellent biocompatibility. The as-prepared nanocarrier system combined the advantages of the superparamagnetic iron oxide nanoparticles and water-soluble graphene sheets, which will find many potential applications in biomedicine and biomaterials.

  15. 聚山梨酯80/Fe3O4复合微球的制备、特性及在靶向MRI中的应用%Preparation, properties of Fe3O4/Polysorbate-80 composite microspheres and their application in MRI

    Institute of Scientific and Technical Information of China (English)

    叶燕斌; 沈晓冬; 崔升; 仲阳; 林本兰

    2011-01-01

    采用化学共沉淀法制备出磁性纳米Fe3O4颗粒,以聚山梨酯80为改性剂制得聚山梨酯80/ Fe3O4复合微球.采用透射电镜( TEM)、X射线衍射仪(XRD)、傅里叶变换红外光谱仪(FTIR)和振动样品磁强计( VSM)对其结构和性能进行了表征.结果表明:Fe3O4颗粒粒径在10~20nm,聚山梨酯80包覆在其表面.复合微球的饱和磁化强度为69.7A·m2/kg.这种复合微球具有很好的分散性和生物相客性,其注射剂作为造影剂应用在新西兰兔的脑靶向性磁共振成像上能够产生很好的T2造影效果.%The magnetic Fe3O4 nanoparticles were prepared by co-precipitation method, then polysorbate-80 as modifier was coated on the surface of Fe3O4 nanoparticles to get Fe3O4/polysorbate-80 composite microspheres. The structure and properties of Fe3O4/polysorbate-80 composite microspheres were characterized by means of transmission electronmicroscopc(TEM), X-ray difrraction(XRD), Fourier transform infrared spectrometry(FTIR) and vibrating sample magnetometcr(VSM). The results showed that the diameter of Fe3O4 nanoparticle is 10-20 nm, polysorbate-80 is well coated on the surface of Fe3O4 nanoparticles. The saturation magnetization of the composite microspheres is 69.7 A-m2/kg. The composite microspheres show good dispersion and biocompatibility, and their injections as contrast agents are well applied in the MRI of brain-targeted to produce very good T2 imaging effect.

  16. Studies on Properties of Rice Straw/Polymer Nanocomposites Based on Polycaprolactone and Fe3O4 Nanoparticles and Evaluation of Antibacterial Activity

    Directory of Open Access Journals (Sweden)

    Roshanak Khandanlou

    2014-10-01

    Full Text Available Modified rice straw/Fe3O4/polycaprolactone nanocomposites (ORS/Fe3O4/ PCL-NCs have been prepared for the first time using a solution casting method. The RS/Fe3O4-NCs were modified with octadecylamine (ODA as an organic modifier. The prepared NCs were characterized by using X-ray powder diffraction (XRD, Scanning electron microscopy (SEM, Transmission electron microscopy (TEM, Thermogravimetric analysis (TGA and Fourier transform infrared spectroscopy (FT-IR. The XRD results showed that as the intensity of the peaks decreased with the increase of ORS/Fe3O4-NCs content in comparison with PCL peaks, the Fe3O4-NPs peaks increased from 1.0 to 60.0 wt. %. The TEM and SEM results showed a good dispersion of ORS/Fe3O4-NCs in the PCL matrix and the spherical shape of the NPs. The TGA analysis indicated thermal stability of ORS/Fe3O4-NCs increased after incorporation with PCL but the thermal stability of ORS/Fe3O4/PCL-NCs decreased with the increase of ORS/Fe3O4-NCs content. Tensile strength was improved with the addition of 5.0 wt. % of ORS/Fe3O4-NCs. The antibacterial activities of the ORS/Fe3O4/PCL-NC films were examined against Gram-negative bacteria (Escherichia coli and Gram-positive bacteria (Staphylococcus aureus by diffusion method using nutrient agar. The results indicated that ORS/Fe3O4/PCL-NC films possessed a strong antibacterial activity with the increase in the percentage of ORS/Fe3O4-NCs in the PCL.

  17. NaCl leached sustainable porous flexible Fe3O4 decorated RGO-polyaniline/PVDF composite for durable application against electromagnetic pollution

    Directory of Open Access Journals (Sweden)

    R. Bera

    2017-05-01

    Full Text Available To avoid the interference of electromagnetic radiation from other devices, an electronic device needs to be fabricated with flexible and light weight electromagnetic interference (EMI shielding materials with high efficiency. According, highly flexible porous poly(vinylidene fluoride (PVDF/PFR (Fe3O4 decorated polyaniline/RGO composite composite was prepared through solution blending of PVDF with pre-synthesized PFR conductive composite that involves in-situ oxidative polymerization of aniline in the presence of reduced graphene oxide (RGO using FeCl3 as oxidant. The porous morphology of the composite was created by leaching out of mixed NaCl from the composite. Polyaniline and RGO were mutually decorated by chemically in-situ synthesized ferrosoferric oxide (Fe3O4 using the Fe source of FeCl3. A homogeneous dispersion of PFR in insulated PVDF matrix resulted in a highly electrical conductive composite (PVDF-PFR material through formation of three dimensional continuous conductive networks of polyaniline-RGO in the matrix phase. The composite shows an outstanding EMI shielding effectiveness (EMI SE property due to the porous structure and the presence of conductive network and ferromagnetic Fe3O4 nanoparticles. The PVDF-PFR composite (0.5 mm thickness depicts a great permittivity and permeability value and achieve high EMI SE value (≈–28.18 dB and conductivity value of ≈1.10·10–1 S·cm–1 at very low loading (5 wt% of RGO.

  18. Study on photocatalytic removal of Congo Red dye wastewater using magnetic Fe3 O4/Carbon nanotubes composite%磁性 Fe3 O4/碳纳米管复合材料光催化处理刚果红染料废水

    Institute of Scientific and Technical Information of China (English)

    宋筱; 朱翩翩; 陈盼; 胡琳; 朱华跃; 蒋茹

    2015-01-01

    Magnetic Fe3 O4/carbon nanotubes ( Fe3 O4/CNTs ) composite was prepared with the co-precipitation method.Crystal phase, particle size and magnetic properties of Fe3 O4/CNTs composite materials were characterized by X-ray diffraction ( XRD) , scanning electron microscopy ( SEM) and vibrating sample magnetometer ( VSM) . Taking Congo Red( CR) dye wastewater treatment as the example, the influence of different factors like treatment processes, photocatalyst dosage, pH and the reuse of photocatalyst on the effectiveness of photocatalytic removal of CR dye wastewater using Fe3 O4/CNTs was studied.The results indicate that 97%of CR solution was successfully decolorized after 50 min under simulated solar light irradiation with 10 mg/L of initial CR concentration and 0.20 g/L of photocatalyst dosage and 0.2 mL of 3% H2 O2 .Over 87% of CR solution ( 10 mg/L ) can be decolorized after the photocatalyst being used for four cycles. In addition to that, the existence of Fe3 O4 nanoparticles makes Fe3 O4/CNTs material have strong magnetism, which means it can be separated easily from treated aqueous by adding magnetic field.%采用共沉淀法制备了一种磁性Fe3O4/CNTs(碳纳米管复合物),采用XRD、SEM、VSM等对Fe3 O4/CNTs复合材料的晶相、颗粒大小和磁性能进行了表征。以刚果红染料废水处理为例,研究了不同处理工艺、催化剂投加量、溶液 pH、催化剂重复使用等因素对Fe3 O4/CNTs材料光催化脱色刚果红染料废水效果的影响。结果表明,当刚果红染料起始质量浓度为10 mg/L,用量为0.2 g/L,3%的H2 O20.2 mL,光照50 min后,Fe3 O4/CNTs对刚果红溶液的脱色率达到97.0%。催化剂重复使用第4次,对刚果红染料的脱色率仍可达87%以上。此外, Fe3 O4纳米粒子的存在使Fe3 O4/CNTs材料具有较强的磁性,且可通过外加磁场将其从处理后的水体中快速分离回收。

  19. Fe3O4@rGO复合磁性粒子对聚氨酯弹性体复合材料性能的影响%Effects of Fe3O4@rGO Composite Magnetic Particles on Properties of Polyurethane Composites

    Institute of Scientific and Technical Information of China (English)

    池慧娟; 孙友谊; 于海林; 刘坦坦; 张文辉; 侯春林; 刘亚青

    2015-01-01

    Three kinds of polyurethane(PUR) elastomer/Fe3O4@reduced graphene oxide(rGO) composites were prepared by incorporating Fe3O4@rGO–tetrahydrofuran(THF) dispersion into PUR elastomer matrix using in-situ polymerization method. The components of the PUR elastomer and PUR/Fe3O4@rGO elastomer composites were characterized by XRD,and the disperse situation was studied by SEM. In addition,the effects of Fe3O4@rGO composite magnetic particles on the thermal,magnetic and mechanical properties of the composite were further investigated in detail. It is found that the Fe3O4@rGO composite magnetic particles have great effects on the properties of the composites. The magnetic,thermal and mechanical properties of the composites are all improved at low loading of 0.5%. At the same time,with the increase of the rGO amount in Fe3O4@rGO composite magnetic particles,the saturation magnetization of the corresponding magnetic composites decrease,and the thermal stability and mechanical properties are gradually increased. When the rGO content in Fe3O4@rGO composite magnetic particles accounted for 60%,PUR/ Fe3O4@rGO composites show higher mechanical properties,which the tensile strength,the elongation at break,the tensile elastic modulus,the glass transition temperature,the maximum loss factor and the storage modulus at–60℃are up to 35.31 MPa, 438.90%,86.42 MPa,10.64℃,0.41 and 3 805.84 MPa,respectively. In addition,Fe3O4@rGO composite magnetic particles have good dispersion in PUR elastomer matrix.%将3种不同的Fe3O4@还原氧化石墨烯(rGO)–四氢呋喃(THF)复合磁性粒子分散液分别与聚氨酯(PUR)弹性体进行原位聚合制备3种PUR弹性体/Fe3O4@rGO磁性复合材料,并对其组分和分散状态进行了表征,系统研究了Fe3O4@rGO复合磁性粒子对PUR弹性体磁性能、热性能和力学性能的影响。结果表明,仅掺入质量分数为0.5%的Fe3O4@rGO复合磁性粒子可以显著提高PUR弹性体的性能。随着Fe3O4@r

  20. Synthesis and characterization of the dual-modified composite Fe3O4/CdSe/CdS magnetic fluorescent compound%双修饰Fe3O4/CdSe/CdS荧光磁性复合物的制备及其表征

    Institute of Scientific and Technical Information of China (English)

    张利杰; 顾银君; 马倩; 刘勇健

    2013-01-01

    采用共沉淀法制得Fe3O4溶胶,用γ-缩水甘油醚氧丙基三甲氧基硅烷(KH-560)对其表面进行改性,制得有机硅改性的纳米Fe3O4磁性粒子;用L-半胱氨酸盐酸盐(L-Cys)将油相的CdSe/CdS转成水相并带上氨基的CdSe/CdS纳米晶;将其复合制备了Fe3O4/CdSe/CdS荧光磁性双功能纳米复合物颗粒.该Fe3O4/CdSe/CdS复合物颗粒平均尺寸约为40nm,饱和磁化强度为21.287A·m2/kg,该纳米粒子既具有优异的荧光特性,也具有较强的超顺磁性.%Fe3O4 magnetic nanoparticles were prepared using hydrothermal coprecipitation process of ferric and ferrous ions.The as-prepared nanoparticles were further modified by γ-(2,3-epoxypropoxy)propytrimethoxysilane (KH-560) to obtain silicone modified Fe3O4 nanoparticles.Also,the water-soluble CdSe/CdS bearing amino have been synthesized using L-cysteine hydrochloride (L-Cys) as stabilizer,At last,CdSe/CdS were linked to Fe3O4 to form luminescent/magnetic bifunctional nanoparticles.The as-prepared composites with a typical diameter of 40nm show 21.287A · m2/kg of saturation magnetic susceptibility.Such material still retains a strong photoluminescence effect of CdSe/CdS quantum dots and also exhibits a typical superparamagnetic behavior of Fe3O4 nanoparticles.

  1. Enzymatic interesterification of soybean oil and methyl stearate blends using lipase immobilized on magnetic Fe3O4/SBA-15 composites as a biocatalyst.

    Science.gov (United States)

    Zang, Xuezhen; Xie, Wenlei

    2014-01-01

    The magnetic Fe3O4/SBA-15 composites were prepared, and treated with 3-aminopropyltriethoxysilane as a carrier material for enzyme immobilization. The immobilization of Candida rugosa lipase onto the amino-functionalized Fe3O4/SBA-15 composite was investigated by using glutaraldehyde as a coupling reagent. The immobilized lipase was then employed as a biocatalyst for the interesterification of soybean oil and methyl stearate in a laboratory-scale operation at 45°C. Various techniques, such as Fourier transform infrared spectroscopy (FT-IR), powder X-ray diffraction (XRD), and vibrating sample magnetometry (VSM), were used for the characterization of the immobilized lipase composite. The immobilized lipase behaved superparamagnetic and showed excellent response at applied magnetic field. The obtained results showed that the immobilized lipase could efficiently catalyze the interesterification reaction. Moreover, the interesterification reaction parameters, such as reaction temperature, substrate ratio and reaction time were investigated regarding the stearoyl incorporation into the triacylglycerols. Further, the immobilized lipase proved to be easily separated from the reaction mixture by applying an external magnetic field and to be stable in the repeated use for four cycles.

  2. 磺丁醚-β-环糊精/Fe3O4杂化的磁性纳米复合体的合成与表征%Synthesis and Characterization of Sulfobutylether-β-cyclodextrin/Fe3O4 Hybrid Magnetic Nano-composite

    Institute of Scientific and Technical Information of China (English)

    曹丽燕; 王海霞; 石娟; 周叶红; 刘文娟; 张国梅; 双少敏

    2011-01-01

    A novel magnetic nano-composite from the combination of Fe3O4 magnetic nanoparticles(MNP) and sulfobutylether-β-CD(SBE-β-CD) has been developed.Fabrication of composite SBE-β-CD/Fe3O4 M NP is based on conjugating the citrate-modified SBE-β-CD onto the gum arabic-modified MNP via carbodiimide activation.The structural property,morphology and hydrodynamic diameter distribution were characterized by X-ray diffraction ( XRD),transmission electron microscopy (TEM) and dynamic light scattering( DLS),respectively.The SBE-β-CD grafting was confirmed by Fourier transformation-infrared spectrometry(FTIR).The amount of SBE-β-CD grafted on MNP and the number of SBE-β-CD molecules immobilized on each MNP were determined by thermogravimetric analysis (TGA).%采用层层自组装法合成了一种新型的磺丁醚-β-环糊精/Fe3O4杂化的磁性纳米复合体(SBE-β-CD/Fe3O4 MNP).β-环糊精与1,4-丁磺酸内酯发生亲核取代反应得到磺丁醚-β-环糊精,柠檬酸进一步修饰磺丁醚-β-环糊精使其具有羧基基团,与阿拉伯胶修饰后的含有氨基的磁性纳米粒子进行脱水缩合制得SBE-β-CD/Fe3O4 MNP.运用X射线衍射(XRD)、透射电镜(TEM)、动态光散射(DLS)、红外光谱法(FHR)和热重分析(TGA)方法进行表征,证实了Fe3O4 MNP上接枝了SBE-β-CD.根据热重分析曲线(TGA)可估算出磁性纳米粒子表面SBE-β-CD的量及每个Fe3O4磁性纳米粒子结合SBE-β-CD分子的个数.

  3. Superhydrophobic and Magnetic Fe3O4/Polydopamine Composite Nanoparticle and Its Oil/Water Separation%超疏水磁性Fe3O4/聚多巴胺复合纳米颗粒及其油/水分离

    Institute of Scientific and Technical Information of China (English)

    梁伟欣; 王贵元; 王奔; 张亚斌; 郭志光

    2013-01-01

    借助于多巴胺在Fe3O4纳米颗粒表面自聚合形成聚多巴胺薄膜制备出Fe3O4/聚多巴胺(Fe3O4/PD)复合纳米颗粒,利用扫描电子显微镜、透射电子显微镜、X射线衍射仪对样品的形貌、结构及成分进行分析.所制备的颗粒经1H,1H,2H,2H-全氟癸基三氯硅烷化学修饰后表现出超疏水性.有趣的是,超疏水性的Fe3O4/PD纳米颗粒包裹在水滴表面能形成磁性液珠,该液珠(4 μL)在亲水性玻璃表面上的接触角高达164°、滚动角为8°.这些磁性液珠具有良好的机械稳定性和强度,同时研究了外部磁场驱动液珠在平面、曲面、油相中运动.结果表明,磁性液珠能够有效应用于操作微流体装置中的液体输送.水滴在Fe3O4/PD纳米颗粒构成表面的接触角超过150°,而油滴则接近0°,因此,在磁场存在下,这些颗粒能用于吸收油水混合物中的油滴而实现油水分离.此外,回收的Fe3O4/PD纳米颗粒保持着超疏水性且能再次利用.%We report a simple approach to creating bifunctional Fe3O4/polydopamine (Fe3O4/PD) composite nanoparticles (NPs) with both superparamagnetic and superhydrophobic properties. The Fe3O4/PD NPs were prepared by virtue of dopa-mine self-polymerization under mild conditions. Their morphology, structure and composition of nanocomposites were analyzed by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), respectively. The Fe3O4/PD NPs have uniform sizes in a narrow range of 100~300 nm. Magnetic measurement reveals the Fe3O4/PD NPs are superparamagnetic with saturation magnetization of 73.40 emu/g. The as-prepared particles showed su-perhydrophobicity after being modified by lH,lH,2H,2H-perfluorodecyltrichlorosilane. The Fe3O4 particles were also modified by fiuoroalkylsilane, and surface composed of the particles present a water contact angle (CA) of 117 °. This result indicated that plenty of phenolic hydroxyl groups in

  4. Facile one-pot fabrication of nano-Fe3O4/carboxyl-functionalized baker's yeast composites and their application in methylene blue dye adsorption

    Science.gov (United States)

    Du, Zongjun; Zhang, Yue; Li, Zhengjie; Chen, Hui; Wang, Ying; Wang, Guangtu; Zou, Ping; Chen, Huaping; Zhang, Yunsong

    2017-01-01

    Nano-Fe3O4/carboxyl-functionalized baker's yeast composites (NF/CF-BYs) were prepared for the first time based on the ultrasonic cavitation assisted oxygen implosion method using single Fe2+ as iron source. The series of characterization analysis results showed that the obtained NF/CF-BYs had not only the superparamagnetic properties of nano-Fe3O4, but their surface also had plenty of functional groups (especially carboxyl groups) introduced by strong oxidization. The adsorption properties of NF/CF-BYs for methylene blue (MB) were also evaluated. The results displayed that the uptakes of NF/CF-BYs for MB were higher than that of pristine baker's yeast (P-BYs), and the adsorption process was followed by the pseudo-second-order kinetic model and Langmuir isotherm. The maximum adsorption capacity of NF/CF-BYs for MB was estimated to be 141.75 mg g-1 at pH 6. The regeneration efficiency of the obtained NF/CF-BYs was attained to be more than 90%.

  5. Sonochemical synthesis of magnetic responsive Fe3O4@TMU-17-NH2 composite as sorbent for highly efficient ultrasonic-assisted denitrogenation of fossil fuel.

    Science.gov (United States)

    Mirzaie, Abbas; Musabeygi, Tahereh; Afzalinia, Ahmad

    2016-08-10

    In this work, a novel magnetic responsive composite was fabricated by encapsulation of Fe3O4 nanoparticles into an amino-functionalized MOF (TMU-17-NH2) under ultrasound irradiation. The prepared materials were characterized by several techniques such as elemental analyses, PXRD, FT-IR, N2 adsorption, TGA and ICP. This composite has been applied to the adsorptive removal of nitrogen-contain compounds in model liquid fuel. The prepared composite demonstrates very good performance for the removal of NCCs. The maximum adsorption capacity of IND and QUI over prepared composite calculated 375.93 and 310.18mg·g(-1) at 25°C, respectively. The composite material is magnetically separable and reusable for several times.

  6. Fe3O4高分子微球联合高强度聚焦超声损伤兔乳腺移植瘤的实验研究%Experiment study of Fe3O4-loaded polymer microspheres for combining with high-intensity focused ultrasound to damage breast cancer of rabbits

    Institute of Scientific and Technical Information of China (English)

    孙阳; 郑元义; 周洋; 沈红霞; 王琦; 王志刚

    2012-01-01

    Objective To prepare the Fe3O4 loaded polymer microspheres(Fe3O4/PLGA),and to investigate the influence of Fe3O4/PLGA combined with high-intensity focused ultrasound (HIFU) on rabbits bearing breast tumor.Methods Double emulsion method were utilized to prepare the Fe3O4/PLGA.14 days after implantation of VX2 tumor in breast,32 rabbits were randomly divided into four equal groups.In group Ⅱ,Ⅲ,and Ⅳ,the rabbits received a percutaneous injection of 0.5 ml saline,PLGA,and Fe3O4/PLGA microcapsules solution into breast tumor at 3,6,9,12 dots,about 3 mm around the tumor respectively,and massaged for 1 min before receiving HIFU ablation,while HIFU group received HIFU ablation only.HIFU ablation parameters were the same:"ablated-dot" mode,acoustic power 150 W,exposure duration 5 s.After HIFU ablation,the volume of coagulative necrosis was calculated,HE staining,TEM and immunohistochemical examination of PCNA were performed to detect the structure changes of the targeted tissue caused by HIFU ablation.Results The volume of coagulative necrosis caused by HIFU ablation was substantially larger and the positive index of PCNA was lower in the necrotic region after the injection of Fe3O4/PLGA microcapsules compared to the group without injection agents,the group of saline and the group of pure PLGA microspheres under the same irritation(P <0.05).Pathological examination demonstrated the targeted tissue was destroyed severely,Fe3O4 nanoparticles were seen depositing in residual tumor cells under TEM.Conclusions The self-made Fe3O4/PLGA microspheres can effectively enhanced the biomedical effect of HIFU surgery on rabbits bearing VX2 breast tumor.%目的 探讨自制载氧化铁高分子微球(Fe3O4/PLGA)联合高强度聚焦超声(HIFU)对兔VX2乳腺癌消融效果的影响.方法 双乳化法制备载Fe3O4的高分子微球.建立兔VX2乳腺癌模型32只,于肿瘤接种后14d,随机分为4组,第1组实验兔给予单纯HIFU辐照;第2、3、4组

  7. Preparation and characterization of chitosan/Fe3 O4/poly(N-isopropylacrylamide-co-acrylic acid)/escherichia coli composite microcapsule%壳聚糖/Fe3 O4/聚(N-异丙基丙烯酰胺-co-丙烯酸)/大肠杆菌复合微囊的制备与表征

    Institute of Scientific and Technical Information of China (English)

    宫艺; 孙敏敏; 朱爱梅; 刘庆林

    2015-01-01

    In order to maintain cell biological activity ,the cell encapsulation with wild condition was developed based on Pickering emulsion ,the Chitosan/Fe3 O4/poly(N-isopropylacrylamide-co-acrylic acid)/Escherichia coli composite microcapsule was prepared and characterized .The P(NIPAM-co-AAc) microgels and oleic acid-modified Fe3 O4 nanoparticles were prepared by microwave-assisted dispersion polymerization and co-precipitation method ,respectively ,and then they were used as the stabilizer to fabricate Pickering emulsion .Chitosan was used to crosslink the P(NIPAM-co-AAc) microgels and Fe3 O4 nanoparticles on the interface of the emulsion droplets which leads to the formation of novel organic/inorganic/biological composite microcapsule .Laser confocal scanning fluorescence microscopy (LCSM ) was used to identify emulsion type of the Pickering emulsion .The morphology and structure of the composite microcapsule was observed by SEM and LCSM .%为了保持细胞的生物活性,基于皮克林乳液开发了条件温和的细胞包裹技术,成功地制备了壳聚糖/Fe3 O4/聚(N-异丙基丙烯酰胺-co-丙烯酸)/大肠杆菌复合微囊。首先采用微波辅助分散聚合法和共沉淀法分别制备了聚(N-异丙基丙烯酰胺-co-丙烯酸)(P(NIPAM-co-AAc))微凝胶与油酸改性的Fe3 O4纳米粒子,并用其作为稳定剂制备皮克林乳液。最后大肠杆菌(E 。 coli)加入水相后分散在乳液液滴内部,使用异硫氰酸荧光素标记的壳聚糖(FITC-CS)交联油水界面的 Fe3O4与 P(NIPAM-AAc)微凝胶形成微囊。通过扫描电镜、透射电镜和激光共聚焦荧光显微镜(LCSM )对制备的凝胶、纳米粒子和复合微囊的形貌结构和组成进行了观察和分析。

  8. 肿瘤治疗用Fe3O4/P(NIPAAm-co-Am)磁性聚合物复合微球的磁热性能%Magnetocaloric effect of Fe3O4/P(NIPAAm-co-Am)composite microspheres for tumor treatment application

    Institute of Scientific and Technical Information of China (English)

    范少勇; 黄科棣; 唐清美; 黄志荣; 艾凡荣; 陈伟高

    2013-01-01

    Research on the magnetic thermo-sensitive composite microspheres for controlled release drug carrier was meaningful.Magnetocaloric effect was used to heat the Fe3O4/P (NIPAAm-co-Am)composite micro-spheres,and the heat generation abilities of the composited microspheres in alternation magnetic field (AMF) were investigated in the present work.Results show the resultant Fe3O4/P(NIPAAm-co-Am)composite mi-crospheres exhibite excellent superparamagnetic and high heating generation ability.The temperature of the composite microspheres was raised after exposed to AMF,which can stimulate the shrinks of P(NIPAAm-co-Am).Furthermore,the temperature raised after exposed to AMF can be adj usted by controlling the concentra-tion of composite microspheres,the magnetic intensity and the frequency of the AMF.%利用磁性纳米粒子在交变磁场作用下的磁热效应,来实现对 Fe3 O4/P(NIPAAm-co-Am)复合微球温度的控制,以达到肿瘤热疗与化疗联合治疗的目的。主要研究了交变磁场作用下复合微球的磁热性能的影响因素。研究结果表明,所制备的 Fe3 O4/P (NIPAAm-co-Am)复合微球具有很好的超顺磁性,且在交变磁场作用下具有很好的磁热效应,其磁热效应可以通过调节微球的浓度、交变磁场的磁场强度和频率等因素来调控,以适应不同应用场合需求。

  9. Solvothermal synthesis and performances of magnetite/reduced graphene oxide composites%溶剂热法制备Fe3O4/氧化石墨烯复合材料及其性能研究∗

    Institute of Scientific and Technical Information of China (English)

    王旭珍; 周泉; 任素贞; 万鹏; 邱介山

    2015-01-01

    Fe3 O4 nanoparticles/reduced graphene oxide (Fe3 O4/RGO)composites were prepared via an in-situ solvothermal synthesis method using graphite oxide and ferrocene as precursors.The structure,morphology, magnetic property and electrochemical performance of the obtained Fe3 O4/RGO hybrids were investigated by X-ray diffraction (XRD),Fourier transform infrared (FT-IR)spectroscopy,scanning and transmission electron microscopy (SEM,TEM),vibrating sample magnetometry (VSM)and cyclic voltammetry test.The results show that magnetic nanoparticles with the average size of 20 nm are well dispersed on the surface of reduced graphene oxide sheets,and the loading amount of Fe3 O4 nanoparticles in the composites can be easily controlled by changing the ratio of ferrocene to graphite oxide in the reaction mixture.The Fe3 O4/RGO composite exhibits superparamagnetic property,as well as good electrochemical stability and rate capability.%以氧化石墨和二茂铁为原料,采用溶剂热法原位一步合成了 Fe3 O4/还原氧化石墨烯(Fe3 O4/RGO)复合物,通过X射线衍射(XRD)、傅里叶变换红外光谱(FT-IR)、扫描电镜(SEM)、透射电镜(TEM)、振动样品磁强计(VSM)、循环伏安测试等手段对复合材料的形貌、结构、磁性能和电化学性能进行了表征。结果表明,该方法具有简单、可控的优点,通过调变前驱物中氧化石墨和二茂铁的比例,可以控制复合物中Fe3 O4纳米粒子的负载量。所制备 Fe3 O4/RGO 复合材料由平均粒径约20 nm 的 Fe3 O4纳米颗粒高度分散在还原氧化石墨烯片层上组成,具有较好的超顺磁性,电化学稳定性和良好的倍率性能。

  10. Cyclodextrin polymer/Fe3O4 nanocomposites as solid phase extraction material coupled with UV-vis spectrometry for the analysis of rutin.

    Science.gov (United States)

    Gong, Aiqin; Ping, Wenhui; Wang, Jue; Zhu, Xiashi

    2014-03-25

    In this paper, carboxymethyl-hydroxypropyl-β-cyclodextrin polymer modified magnetic particles Fe3O4 (CM-HP-β-CDCP-MNPs) were prepared and applied to magnetic solid phase extraction of rutin combined with UV-visible spectrometry detection. The synthesized magnetic particles were characterized by element analysis, Fourier transform infrared spectra, thermal gravimetric analysis, and transmission electron microscopy. Several variables affecting the extraction and desorption of rutin such as pH, the amount of adsorbent, the type and volume of eluent, extraction and desorption time, and temperature were investigated. The maximum adsorption capacity was 67.0 mg g(-1) for rutin with the equilibrium time of 30 min at room temperature, and the adsorbent could be reused for 10 times. A calibration curve was linear in the range of 0.05-8.00 μg mL(-1) with a relative standard deviation of 2.9% (n=5, c=4.0 μg mL(-1)). The limit of detection was 7.0 ng mL(-1). The interaction mechanism between the adsorbent and rutin was also studied. Feasibility of this method was validated by the analysis of rutin tablets and lotus plumule. Copyright © 2013 Elsevier B.V. All rights reserved.

  11. Cyclodextrin polymer/Fe3O4 nanocomposites as solid phase extraction material coupled with UV-vis spectrometry for the analysis of rutin

    Science.gov (United States)

    Gong, Aiqin; Ping, Wenhui; Wang, Jue; Zhu, Xiashi

    2014-03-01

    In this paper, carboxymethyl-hydroxypropyl-β-cyclodextrin polymer modified magnetic particles Fe3O4 (CM-HP-β-CDCP-MNPs) were prepared and applied to magnetic solid phase extraction of rutin combined with UV-visible spectrometry detection. The synthesized magnetic particles were characterized by element analysis, Fourier transform infrared spectra, thermal gravimetric analysis, and transmission electron microscopy. Several variables affecting the extraction and desorption of rutin such as pH, the amount of adsorbent, the type and volume of eluent, extraction and desorption time, and temperature were investigated. The maximum adsorption capacity was 67.0 mg g-1 for rutin with the equilibrium time of 30 min at room temperature, and the adsorbent could be reused for 10 times. A calibration curve was linear in the range of 0.05-8.00 μg mL-1 with a relative standard deviation of 2.9% (n = 5, c = 4.0 μg mL-1). The limit of detection was 7.0 ng mL-1. The interaction mechanism between the adsorbent and rutin was also studied. Feasibility of this method was validated by the analysis of rutin tablets and lotus plumule.

  12. Magnetic Solid-phase Extraction with Fe3O4/Molecularly Imprinted Polymers Modified by Deep Eutectic Solvents and Ionic Liquids for the Rapid Purification of Alkaloid Isomers (Theobromine and Theophylline from Green Tea

    Directory of Open Access Journals (Sweden)

    Guizhen Li

    2017-06-01

    Full Text Available Different kinds of deep eutectic solvents (DES based on choline chloride (ChCl and ionic liquids (ILs based on 1-methylimidazole were used to modify Fe3O4/molecularly imprinted polymers (Fe3O4/MIPs, and the resulting materials were applied for the rapid purification of alkaloid isomers (theobromine and theophylline from green tea with magnetic solid-phase extraction (M-SPE. The M-SPE procedure was optimized using the response surface methodology (RSM to analyze the maximum conditions. The materials were characterized by Fourier transform infrared spectroscopy (FI-IR and field emission scanning electron microscopy (FE-SEM. Compared to the ILs-Fe3O4/MIPs, the DESs-Fe3O4/MIPs were developed for the stronger recognition and higher recoveries of the isomers (theophylline and theobromine from green tea, particularly DES-7-Fe3O4/MIPs. With RSM, the optimal recovery condition for theobromine and theophylline in the M-SPE were observed with ratio of methanol (80% as the washing solution, methanol/acetic acid (HAc (8:2 as the eluent at pH 3, and an eluent volume of 4 mL. The practical recoveries of theobromine and theophylline in green tea were 92.27% and 87.51%, respectively, with a corresponding actual extraction amount of 4.87 mg•g−1 and 5.07 mg•g−1. Overall, the proposed approach with the high affinity of Fe3O4/MIPs might offer a novel method for the purification of complex isomer samples.

  13. The compositional, structural, and magnetic properties of a Fe3O4/Ga2O3/GaN spin injecting hetero-structure grown by metal-organic chemical vapor deposition

    Science.gov (United States)

    Xu, Zhonghua; Huang, Shimin; Tang, Kun; Gu, Shulin; Zhu, Shunming; Ye, Jiandong; Xu, Mingxiang; Wang, Wei; Zheng, Youdou

    2016-12-01

    In this article, the authors have designed and fabricated a Fe3O4/Ga2O3/GaN spin injecting hetero-structure by metal-organic chemical vapor deposition. The compositional, structural, and magnetic properties of the hetero-structure have been characterized and discussed. From the characterizations, the hetero-structure has been successfully grown generally. However, due to the unintentional diffusion of Ga ions from Ga2O3/GaN layers, the most part of the nominal Fe3O4 layer is actually in the form of GaxFe3-xO4 with gradually decreased x values from the Fe3O4/Ga2O3 interface to the Fe3O4 surface. Post-annealing process can further aggravate the diffusion. Due to the similar ionic radius of Ga and Fe, the structural configuration of the GaxFe3-xO4 does not differ from that of pure Fe3O4. However, the ferromagnetism has been reduced with the incorporation of Ga into Fe3O4, which has been explained by the increased Yafet-Kittel angles in presence of considerable amount of Ga incorporation. A different behavior of the magnetoresistance has been found on the as-grown and annealed samples, which could be modelled and explained by the competition between the spin-dependent and spin-independent conduction channels. This work has provided detailed information on the interfacial properties of the Fe3O4/Ga2O3/GaN spin injecting hetero-structure, which is the solid basis for further improvement and application of the structure.

  14. PLLA- Fe3O4 nanocomposites

    Science.gov (United States)

    Albano, Carmen; Gonzalez, Gema; Naranjo, Claudio

    2012-07-01

    In the present work magnetite nanoparticules and PLLA- Fe3O4 nanocomposites were prepared by high frequency ultrasound. The influence of pH on nanoparticle size was studied, showing that the particle size decreased as the pH increased. In the composites an interaction between the magnetite nanoparticles and the PLLA matrix was observed by FTIR. Magnetic properties were studied using a VSM, and a superparamegnetic behavior was observed for magnetite nanoparticles, but for the composite a magnetic attenuation was observed due to the polymeric matrix.

  15. Superparamagnetic Fe3 O4 @SiO2 core-shell composite nanoparticles for the mixed hemimicelle solid-phase extraction of benzodiazepines from hair and wastewater samples before high-performance liquid chromatography analysis.

    Science.gov (United States)

    Esmaeili-Shahri, Effat; Es'haghi, Zarrin

    2015-12-01

    Magnetic Fe3 O4 /SiO2 composite core-shell nanoparticles were synthesized, characterized, and applied for the surfactant-assisted solid-phase extraction of five benzodiazepines diazepam, oxazepam, clonazepam, alprazolam, and midazolam, from human hair and wastewater samples before high-performance liquid chromatography with diode array detection. The nanocomposite was synthesized in two steps. First, Fe3 O4 nanoparticles were prepared by the chemical co-precipitation method of Fe(III) and Fe(II) as reaction substrates and NH3 /H2 O as precipitant. Second, the surface of Fe3 O4 nanoparticles was modified with shell silica by Stober method using tetraethylorthosilicate. The Fe3 O4 /SiO2 composite were characterized by X-ray diffraction, scanning electron microscopy, Fourier transform infrared spectroscopy, and vibrating sample magnetometry. To enhance their adsorptive tendency toward benzodiazepines, cetyltrimethylammonium bromide was added, which was adsorbed on the surface of the Fe3 O4 /SiO2 nanoparticles and formed mixed hemimicelles. The main parameters affecting the efficiency of the method were thoroughly investigated. Under optimum conditions, the calibration curves were linear in the range of 0.10-15 μgmL(-1) . The relative standard deviations ranged from 2.73 to 7.07%. The correlation coefficients varied from 0.9930 to 0.9996.

  16. Core-double-shell Fe3O4@carbon@poly(In(III)-carboxylate) microspheres: cycloaddition of CO2 and epoxides on coordination polymer shells constituted by imidazolium-derived Al(III)-Salen bifunctional catalysts.

    Science.gov (United States)

    An, Qiao; Li, Zifeng; Graff, Robert; Guo, Jia; Gao, Haifeng; Wang, Changchun

    2015-03-01

    A hydrid microsphere Fe3O4@carbon@poly(In(III)-carboxylate) consisting of a cluster of Fe3O4 nanoparticles as the core, a carbon layer as the inner shell and a porous In(III)-carboxylate coordination polymer as the outer shell was prepared and applied as a recyclable catalyst for the cycloaddition reaction of CO2 and epoxides. Construction of this hybrid microsphere was achieved in the two steps, including (1) the one-pot solvothermal synthesis of Fe3O4@C particles with the abundant carboxylic groups on the carbon surface and (2) the subsequent growth of the outer shell polymers based on the precipitation coordination polymerization. Imidazolium-substituted Salen ligands were synthesized and chelated with the In(III) ions using the terminal carboxylic groups. The coordination polymer shell was formed on the Fe3O4@C particles, and the structures including shell thickness, surface area and porosity could be varied by tuning the feeding ratios of the In(III) ions and the ligands. The optimal structure of the coordination polymers showed a shell thickness of ca. 45 nm with ∼5 nm of mesopore, 174.7 m(2)/g of surface area and 0.2175 cm(3)/g of pore volume. In light of gas uptake capability, catalytic activity and magnetic susceptibility, cycloaddition of CO2 with a series of epoxides were studied by using Al-complexed Fe3O4@C@In(III)-[IL-Salen] microspheres. The results validated that the self-supporting catalytic layer with high surface area was of remarkable advantages, which were attributed from great increment of effective active sites and combination of nucleophilic/electrophilic synergistic property and CO2 uptake capability. Therefore, these hybrid microspheres provided excellent catalytic activity, prominent selectivity to cyclic carbonates and outstanding recyclability with the assistance of an applied magnetic field.

  17. Photocatalytic activity of cerium-doped mesoporous TiO2 coated Fe3O4magnetic composite under UV and visible light

    Institute of Scientific and Technical Information of China (English)

    SHI Zhongliang; YANG Xingman; YAO Shuhua

    2012-01-01

    A novel kind of magnetically separable photocatalyst of cerrium-doped mesoporous titanium dioxide coated magnetite (Ce/MTiO2/Fe3O4) was prepared and its activities under UV and visible light were reported.The catalysts with Ce/MTiO2 shell and Fe3O4 core were prepared by coating photoactive Ce/MTiO2 onto a magnetic Fe3O4 core through the hydrolysis of tetrabutyltitanate (Ti(OBu)4,TBT) with precursors of ammonium ceric nitrate and TBT in the presence of Fe3O4 particles.The MTiO2 shell was for photocatalysis,the Fe3O4 core was for separation by the magnetic field and the doped Ce was used to enhance the photocatalytic activity of MTiO2.The morphological,structural and optical properties of the prepared samples were characterized by Brunauer-Emmett-Teller (BET) surface area,transmission electron microscopy (TEM),X-ray diffraction (XRD) and UV-vis absorption spectroscopy.The effect of cerrium-doped content on the photocatalytic activity was studied and the result revealed that 0.5 mol.% Ce/MTiO2/Fe3O4 exhibited highest photoactivity.The photocatalytic activities of obtained photocatalysts under UV and visible light were estimated by measuring the degradation rate of methylene blue (MB,50 mg/L) in an aqueous solution.The results showed that the prepared photocatalyst was activated by visible light and used as effective catalyst in photooxidation reactions.In addition,the possibility of cyclic usage of the prepared photocatalyst was also confirmed.Moreover,Ce/MTiO2 was tightly bound to Fe3O4 and could be easily recovered from the medium by an external magnetic filed.So,the photocatalyst can be reused without any mass loss.It can therefore be potentially applied for the treatment of water contaminated by organic pollutants.

  18. PEGylated FePt-Fe3O4 composite nanoassemblies (CNAs): in vitro hyperthermia, drug delivery and generation of reactive oxygen species (ROS).

    Science.gov (United States)

    Sahu, Niroj Kumar; Gupta, Jagriti; Bahadur, Dhirendra

    2015-05-21

    Chemothermal therapy is widely used in clinical applications for the treatment of tumors. However, the major challenge is the use of a multifunctional nano platform for significant regression of the tumor. In this study, a simple synthesis of highly aqueous stable, carboxyl enriched, PEGylated mesoporous iron platinum-iron(ii,iii) oxide (FePt-Fe3O4) composite nanoassemblies (CNAs) by a simple hydrothermal approach is reported. CNAs exhibit a high loading capacity ∼90 wt% of the anticancer therapeutic drug, doxorubicin (DOX) because of its porous nature and the availability of abundant negatively charged carboxylic groups on its surface. DOX loaded CNAs (CNAs + DOX) showed a pH responsive drug release in a cell-mimicking environment. Furthermore, the release was enhanced by the application of a alternating current magnetic field. CNAs show no appreciable cytotoxicity in mouse fibroblast (L929) cells but show toxic effects in cervical cancer (HeLa) cells at a concentration of ∼1 mg mL(-1). A suitable composition of CNAs with a concentration of 2 mg mL(-1) can generate a hyperthermic temperature of ∼43 °C. Also, CNAs, because of their Fe and Pt contents, have an ability to generate reactive oxygen species (ROS) in the presence of hydrogen peroxide inside the cancer cells which helps to enhance its therapeutic effects. The synergistic combination of chemotherapy and ROS is very efficient for killing cancer cells.

  19. Preparation of Fe3O4/P(GMA-co-EGDMA) magnetic composite microspheres with high specific surface area by deposition of porous template%模板沉积法制备大孔高比表面积Fe3O4/P( GMA-co-EGDMA)磁性复合微球

    Institute of Scientific and Technical Information of China (English)

    张宝亮; 张秋禹; 张和鹏; 范新龙; 厉向杰; 雷星锋

    2012-01-01

    A simple method for preparation of Fe3O4/P ( GMA-co-EGDMA) magnetic composite microspheres using microporous P(GMA-co-EGDMA) microspheres copolymerized with glycidyl methacrylate (GMA) and ethylene glycol dimethacrylate (EGDMA) as template is reported in this paper. The preparation process included soaking of ferrous ion and ferric ion and coprecipitation in the presence of OH" . The influences of soaking temperature, soaking time, coprecipitation temperature and deposition times on magnetic content of magnetic composite microspheres were studied. The optimum preparation process of microporous Fe3O4/P (GMA-co-EGDMA) magnetic composite microspheres was as follows: microporous P (GMA-co-EGDMA) microspheres were soaked at 50°Cfor 4 h, coprecipitation temperature and time were 70°C and 1 h respectively. The magnetic content of magnetic composite microsphereswas 45. 24% when the deposition process was repeated 4 times. The morphology, magnetic properties, magnetic content, pore performance and particle size distribution of Fe3O4/P (GMA-co-EGDMA) were determined by SEM, TGA, XRD, mercury porosimeter and laser particle sizer. It was found that the range of particle size of Fe3O4/P (GMA-co-EGDMA) was 100~200 jmm and average particle size was 162 j^m, specific saturation magnetization was 10. 92 emu ? G~J , average pore diameter and specific surface area were 60 nm and 116 m2 ? G"1 respectively.%介绍了一种以大孔高比表面积甲基丙烯酸缩水甘油酯(GMA)与二甲基丙烯酸乙二醇酯(EGDMA)共聚交联微球[P(GMA-co-EGDMA)]为模板制备磁性复合微球的简单方法.制备过程包括Fe3+和Fe2+的浸入、OH-作用下孔内铁离子的共沉淀两步.在此过程中考察了浸泡温度、浸泡时间、共沉淀温度以及沉积次数对微球磁含量的影响,确定最佳制备工艺为50℃浸泡4h,70℃反应1h,如此反复4次磁含量可以达到45.24%.并通过SEM、VSM、XRD、TGA及压汞仪、激光粒度仪等手段对Fe3O4/P( GMA

  20. Electrical conductivity of LaFeO3.xFe3O4 (x = 0.0, 0.1, 0.2, 0.3, and 0.4) composites materials

    Science.gov (United States)

    Laysandra, H.; Triyono, D.

    2017-07-01

    Electrical conductivity of composites material LaFeO3.xFe3O4 with x = 0.0, 0.1, 0.2, 0.3, and 0.4 have been studied by impedance spectroscopy method. LaFeO3 was synthesized by sol-gel method result in nanoparticle, then it mixed with Fe3O4 powder, homogeneously. The mixture was pressed into pellet and sintered at 1300 °C for 1 h to form LaFeO3.xFe3O4 composites materials. The electrical properties as a function of temperature (300 K - 500 K) and frequency (100 Hz - 1 MHz) were presented in Nyquist and Bode plot. From these plots, the equivalent circuit was found and their parameters are contributed by grain and grain boundary which is supported by morphology characterized by scanning electron microscopy (SEM). DC conductivity of LaFeO3.xFe3O4 as a function of temperature was explained by using Arrhenius equation of 1000/T vs ln σ. From this equation, the values of the activation energy (Ea) for all samples were calculated. The value of Ea can be also analyzed as grain and grain boundary contribution.

  1. 3-D graphene-supported mesoporous SiO2 @Fe3 O4 composites for the analysis of pesticides in aqueous samples by magnetic solid-phase extraction with high-performance liquid chromatography.

    Science.gov (United States)

    Wang, Xuemei; Wang, Huan; Lu, Muxin; Ma, Xiaomin; Huang, Pengfei; Lu, Xiaoquan; Du, Xinzhen

    2016-05-01

    Three-dimensional graphene-supported mesoporous silica@Fe3 O4 composites (mSiO2 @Fe3 O4 -G) were prepared by modifying mesoporous SiO2 -coated Fe3 O4 onto hydrophobic graphene nanosheets through a simple adsorption co-condensation method. The obtained composites possess unique properties of large surface area (332.9 m(2) /g), pore volume (0.68 cm(3) /g), highly open pore structure with uniform pore size (31.1 nm), as well as good magnetic separation properties. The adsorbent (mSiO2 @Fe3 O4 -G) was used for the magnetic solid-phase extraction of seven pesticides with benzene rings in different aqueous samples before high-performance liquid chromatography. The main parameters affecting the extraction such as adsorbent amount, volume of elution solvent, time of extraction and desorption, salt effect, oscillation rate were investigated. Under the optimal conditions, this method provided low limits of detection (S/N = 3, 0.525-3.30 μg/L) and good linearity (5.0-1000 μg/L, R(2) > 0.9954). Method validation proved the feasibility of the developed adsorbent, which has a high extraction efficiency and excellent enhancement performance for pesticides in this study. The proposed method was successfully applied to real aqueous samples, and satisfactory recoveries ranging from 77.5 to 113.6% with relative standard deviations within 9.7% were obtained.

  2. Magnetic and structural characteristics of multiferroic Fe3O4/(Bi3.25Nd0.65Eu0.10)Ti3O12 composite thin films deposited by metalorganic chemical vapor deposition

    Science.gov (United States)

    Kobune, Masafumi; Furotani, Ryosuke; Fujita, Satoshi; Kikuchi, Kazuki; Kikuchi, Takeyuki; Fujisawa, Hironori; Shimizu, Masaru; Fukumuro, Naoki

    2016-10-01

    Ferromagnetic magnetite (Fe3O4) thin films for magnetoelectric multiferroic applications were deposited on (200) (Bi3.25Nd0.65Eu0.10)Ti3O12 (BNEuT)/(101) Nb:TiO2 substrates by metalorganic chemical vapor deposition (MOCVD) using an iron(III) tris(2,2,6,6-tetramethyl-3,5-heptanedionato) precursor as the iron source. The BNEuT film utilized as a ferroelectric template material was in the form of freestanding nanoplates with narrow spaces between them. The effects of deposition conditions such as the deposition time and substrate temperature on the magnetic and structural characteristics of the Fe3O4/BNEuT composite films were investigated. All the films consisted of mostly single-phase Fe3O4 with a cubic inverse-spinel structure. When deposition was carried out at temperatures of 400-420 °C, the filling rates of particles introduced into the narrow spaces between the BNEuT nanoplates exhibited high values of 76-89% including the amorphous phase. This suggested that the deposition in this temperature range made progress according to the growth mechanism of MOCVD in the surface reaction rate determining state. Room-temperature magnetic moment-magnetic field curves for Fe3O4 thin films deposited at 400-500 °C for 60 min exhibited narrow rectangular hysteresis loops, indicating typical soft magnetic characteristics.

  3. Synthesis, Characterization, and Study of In Vitro Cytotoxicity of ZnO-Fe3O4 Magnetic Composite Nanoparticles in Human Breast Cancer Cell Line (MDA-MB-231) and Mouse Fibroblast (NIH 3T3).

    Science.gov (United States)

    Bisht, Gunjan; Rayamajhi, Sagar; Kc, Biplab; Paudel, Siddhi Nath; Karna, Deepak; Shrestha, Bhupal G

    2016-12-01

    Novel magnetic composite nanoparticles (MCPs) were successfully synthesized by ex situ conjugation of synthesized ZnO nanoparticles (ZnO NPs) and Fe3O4 NPs using trisodium citrate as linker with an aim to retain key properties of both NPs viz. inherent selectivity towards cancerous cell and superparamagnetic nature, respectively, on a single system. Successful characterization of synthesized nanoparticles was done by XRD, TEM, FTIR, and VSM analyses. VSM analysis showed similar magnetic profile of thus obtained MCPs as that of naked Fe3O4 NPs with reduction in saturation magnetization to 16.63 emu/g. Also, cell viability inferred from MTT assay showed that MCPs have no significant toxicity towards noncancerous NIH 3T3 cells but impart significant toxicity at similar concentration to breast cancer cell MDA-MB-231. The EC50 value of MCPs on MDA-MB-231 is less than that of naked ZnO NPs on MDA-MB-231, but its toxicity on NIH 3T3 was significantly reduced compared to ZnO NPs. Our hypothesis for this prominent difference in cytotoxicity imparted by MCPs is the synergy of selective cytotoxicity of ZnO nanoparticles via reactive oxygen species (ROS) and exhausting scavenging activity of cancerous cells, which further enhance the cytotoxicity of Fe3O4 NPs on cancer cells. This dramatic difference in cytotoxicity shown by the conjugation of magnetic Fe3O4 NPs with ZnO NPs should be further studied that might hold great promise for the development of selective and site-specific nanoparticles. Schematic representation of the conjugation, characterization and cytotoxicity analysis of Fe3O4-ZnO magnetic composite particles (MCPs).

  4. Synthesis, Characterization, and Study of In Vitro Cytotoxicity of ZnO-Fe3O4 Magnetic Composite Nanoparticles in Human Breast Cancer Cell Line (MDA-MB-231) and Mouse Fibroblast (NIH 3T3)

    Science.gov (United States)

    Bisht, Gunjan; Rayamajhi, Sagar; KC, Biplab; Paudel, Siddhi Nath; Karna, Deepak; Shrestha, Bhupal G.

    2016-12-01

    Novel magnetic composite nanoparticles (MCPs) were successfully synthesized by ex situ conjugation of synthesized ZnO nanoparticles (ZnO NPs) and Fe3O4 NPs using trisodium citrate as linker with an aim to retain key properties of both NPs viz. inherent selectivity towards cancerous cell and superparamagnetic nature, respectively, on a single system. Successful characterization of synthesized nanoparticles was done by XRD, TEM, FTIR, and VSM analyses. VSM analysis showed similar magnetic profile of thus obtained MCPs as that of naked Fe3O4 NPs with reduction in saturation magnetization to 16.63 emu/g. Also, cell viability inferred from MTT assay showed that MCPs have no significant toxicity towards noncancerous NIH 3T3 cells but impart significant toxicity at similar concentration to breast cancer cell MDA-MB-231. The EC50 value of MCPs on MDA-MB-231 is less than that of naked ZnO NPs on MDA-MB-231, but its toxicity on NIH 3T3 was significantly reduced compared to ZnO NPs. Our hypothesis for this prominent difference in cytotoxicity imparted by MCPs is the synergy of selective cytotoxicity of ZnO nanoparticles via reactive oxygen species (ROS) and exhausting scavenging activity of cancerous cells, which further enhance the cytotoxicity of Fe3O4 NPs on cancer cells. This dramatic difference in cytotoxicity shown by the conjugation of magnetic Fe3O4 NPs with ZnO NPs should be further studied that might hold great promise for the development of selective and site-specific nanoparticles.

  5. Fe3O4@TiO2复合纳米颗粒稳定Pickering乳液的光磁双响应性研究%Pickering emulsion stabilized by Fe3O4@TiO2 core-shell composite nanoparticles with light and magnetic response

    Institute of Scientific and Technical Information of China (English)

    张青; 白瑞雪; 张志雄; 申小林; 张帆; 郭婷; 童志平; 孟涛

    2016-01-01

    利用三甲基氯硅烷修饰的核壳结构Fe3O4@TiO2复合纳米颗粒来稳定Pickering乳液,并对乳液的磁响应性和光响应性进行了评价,结果表明:Fe3O4@TiO2复合纳米颗粒稳定的Pickering乳液具有良好的磁响应性和光响应特性.

  6. In vitro biocompatibility of magnetic thermo-responsive nanohydrogel particles of poly(N-isopropylacrylamide-co-acrylic acid) with Fe3O4 cores: effect of particle size and chemical composition.

    Science.gov (United States)

    Chou, Feng-Yi; Lai, Jui-Yang; Shih, Chao-Ming; Tsai, Meng-Chao; Lue, Shingjiang Jessie

    2013-04-01

    Biocompatibility is a critical factor in the design and development of candidate materials for biomedical use. This paper reports on the in vitro biocompatibility of magnetic stimuli-sensitive nanohydrogel particles composed of magnetite cores in poly(N-isopropylacrylamide-co-acrylic acid) shells referred to Fe(3)O(4)/P(NIPAAm-co-AAc). The AAc concentration and polymerization time were varied to fabricate magnetic nanoparticles with various AAc levels (1.80-2.37%) and particle sizes (74-213 nm). The P(NIPAAm-co-AAc) shell exhibited thermo-sensitive properties and the Fe(3)O(4) core constituted 2.25-4.10% of the particles by weight. After a 2-day incubation of L929 cells with extract media that had been conditioned with various test samples, the cellular responses were monitored in terms of cell viability and growth. The Live/Dead assays showed that high levels of cellular viability (97.3-98.1%) were observed in all groups, indicating that none of the nanoparticles were cytotoxic. However, the 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymetho-xyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium (MTS) assays demonstrated that the activity of mitochondrial dehydrogenase varied significantly in cultures exposed to different magnetic nanohydrogel particles. The murine fibroblasts exposed to the NIP-(AAc5.1-Fe)-2 sample, which contained the highest AAc content and largest particle sizes, were the least metabolically active. In contrast, the activity levels in the cultures treated with the low AAc content and small size particles (NIP-(AAc2.6-Fe)-1) were not significantly different from those in the control group. Our findings suggest that smaller magnetic stimuli-sensitive nanohydrogel particles with a lower AAc content may have little inhibitory impact on cell proliferation. Overall, the in vitro biocompatibilities of the nanoparticles depend on the chemical composition and size of the Fe(3)O(4)/P(NIPAAm-co-AAc) particles.

  7. Fe3O4@SiO2-TiO2磁性介孔复合材料光催化降解亚甲基蓝的性能研究%Study on Magnetic Fe3 O4@ mesoSiO2 -TiO2 Mesoporous Composites Photocatalytic Degradation of Methylene Blue

    Institute of Scientific and Technical Information of China (English)

    谢焕玲; 贺卫; 陈格; 全学军; 杨桔材

    2014-01-01

    染料废水处理是水污染治理中非常重要内容之一,针对染料废水带有极高的色度、可生化性差和含“三致”物等特点。本文采用水热法制备复合材料用于染料废水处理。通过XRD、T EM、SBET 等表征手段证实制备材料为核-壳Fe3 O4@ SiO2-T iO2复合材料。将此材料用于染料废水处理,选用亚甲基蓝(Methylene Blue ,简称MB)作为染料废水典型目标物,测定催化剂Ti:Si摩尔比、催化剂用量、染料溶液pH值和催化剂重复利用对染料废水降解效果影响。研究结果表明,染料废水浓度为14mg/L ,双氧水用量为2mL ,催化剂用量为2g/L ,脱色90min时,溶液脱色率能达到98.6%。催化剂重复使用4次,其脱色效果仍然保持在90%左右。由此可见,用此方法制备的核-壳材料是比较有效且实用的一种染料废水处理非均相Fenton催化剂。%Dyestuff textile wastewater treatment has become a research hotspot due to it ’s high chroma ,poor biodegradability ,and low toxicity characteristics .In this paper ,we have synthesized composite materials by hydrothermal methods .Core-shell Fe3 O4@ SiO2 -TiO2 materials were charac-terized by XRD ,TEM and so on .This materials have been applied to dye wastewater treatment . Methylene blue was used as typical target of dye wastewater .Degradation effects of dye wastewater were determined by catalyst with different Ti :Si molar ratios ,amount of catalyst ,pH value of the dye solution and catalyst reuse . A serious of results of study show that decolorization ratios of dye wastewater arrived at 98 .6% under optimal conditions .When catalysts were reused for 4 times ,it’s decolorization ratios were maintained at about 90% . Therefore , this materials synthesized by this methods is an effective and practical dye wastewater treatment catalysts .

  8. Fluorescence analysis of 6-mercaptopurine with the use of a nano-composite consisting of BSA-capped Au nano-clusters and core-shell Fe3O4-SiO2 nanoparticles.

    Science.gov (United States)

    Li, Zhuo; Wang, Yong; Ni, Yongnian; Kokot, Serge

    2015-08-15

    A magnetic and fluorescent nano-composite was prepared. It comprised of a core of Fe3O4 nanoparticles (NPs), a silica shell and satellitic Au nano-clusters (AuNCs) capped with bovine serum albumin (BSA). This nano-composite has many desirable properties, e.g. magnetism, red emission, high water solubility, and high resistance to photo-bleaching. On addition of the analyte, 6-mercaptopurine (6-MP) or indeed other similar thiols, AuNCs formed aggregates because the existing cross-links within the Fe3O4 NPs@SiO2 and AuNC structure were broken in favor of the gold-thiol bonds. On suitable irradiation of such aggregates, red fluorescence was emitted at 613 nm. It decreased significantly as a function of the added 6-MP concentration, and the quenching ratio (F0 - F) / F0 was related linearly to the concentration of 6-MP in the range of 0.01 to 0.5 μmol L(-1). The detection limit was 0.004 μmol L(-1) (S/N=3). The method was strongly selective for 6-MP in the presence of oxidants, phenols, heavy-metal ions, and especially bio-thiols.

  9. Sandwich-Structured Graphene-Fe3O4@Carbon Nanocomposites for High-Performance Lithium-Ion Batteries.

    Science.gov (United States)

    Zhao, Li; Gao, Miaomiao; Yue, Wenbo; Jiang, Yang; Wang, Yuan; Ren, Yu; Hu, Fengqin

    2015-05-13

    Advanced anode materials for high power and high energy lithium-ion batteries have attracted great interest due to the increasing demand for energy conversion and storage devices. Metal oxides (e.g., Fe3O4) usually possess high theoretical capacities, but poor electrochemical performances owing to their severe volume change and poor electronic conductivity during cycles. In this work, we develop a self-assembly approach for the synthesis of sandwich-structured graphene-Fe3O4@carbon composite, in which Fe3O4 nanoparticles with carbon layers are immobilized between the layers of graphene nanosheets. Compared to Fe3O4@carbon and bulk Fe3O4, graphene-Fe3O4@carbon composite shows superior electrochemical performance, including higher reversible capacity, better cycle and rate performances, which may be attributed to the sandwich structure of the composite, the nanosized Fe3O4, and the carbon layers on the surface of Fe3O4. Moreover, compared to the reported graphene-Fe3O4 composite, the particle size of Fe3O4 is controllable and the content of Fe3O4 in this composite can be arbitrarily adjusted for optimal performance. This novel synthesis strategy may be employed in other sandwich-structured nanocomposites design for high-performance lithium-ion batteries and other electrochemical devices.

  10. Magnetic biodegradable Fe3O4/CS/PVA nanofibrous membranes for bone regeneration.

    Science.gov (United States)

    Wei, Yan; Zhang, Xuehui; Song, Yu; Han, Bing; Hu, Xiaoyang; Wang, Xinzhi; Lin, Yuanhua; Deng, Xuliang

    2011-10-01

    In recent years, interest in magnetic biomimetic scaffolds for tissue engineering has increased considerably. The aim of this study is to develop magnetic biodegradable fibrous materials with potential use in bone regeneration. Magnetic biodegradable Fe(3)O(4)/chitosan (CS)/poly vinyl alcohol (PVA) nanofibrous membranes were achieved by electrospinning with average fiber diameters ranging from 230 to 380 nm and porosity of 83.9-85.1%. The influences of polymer concentration, applied voltage and Fe(3)O(4) nanoparticles loading on the fabrication of nanofibers were investigated. The polymer concentration of 4.5 wt%, applied voltage of 20 kV and Fe(3)O(4) nanoparticles loading of lower than 5 wt% could produce homogeneous, smooth and continuous Fe(3)O(4)/CS/PVA nanofibrous membranes. X-ray diffraction (XRD) data confirmed that the crystalline structure of the Fe(3)O(4), CS and PVA were maintained during electrospinning process. Fourier transform infrared spectroscopy (FT-IR) demonstrated that the Fe(3)O(4) loading up to 5 wt% did not change the functional groups of CS/PVA greatly. Transmission electron microscopy (TEM) showed islets of Fe(3)O(4) nanoparticles evenly distributed in the fibers. Weak ferrimagnetic behaviors of membranes were revealed by vibrating sample magnetometer (VSM) test. Tensile test exhibited Young's modulus of membranes that were gradually enhanced with the increase of Fe(3)O(4) nanoparticles loading, while ultimate tensile stress and ultimate strain were slightly reduced by Fe(3)O(4) nanoparticles loading of 5%. Additionally, MG63 human osteoblast-like cells were seeded on the magnetic nanofibrous membranes to evaluate their bone biocompatibility. Cell growth dynamics according to MTT assay and scanning electron microscopy (SEM) observation exhibited good cell adhesion and proliferation, suggesting that this magnetic biodegradable Fe(3)O(4)/CS/PVA nanofibrous membranes can be one of promising biomaterials for facilitation of osteogenesis.

  11. Magnetite Fe3O4 nanoparticles synthesis by wet chemical reduction and their characterization

    Science.gov (United States)

    Chaki, S. H.; Malek, Tasmira J.; Chaudhary, M. D.; Tailor, J. P.; Deshpande, M. P.

    2015-09-01

    The authors report the synthesis of Fe3O4 nanoparticles by wet chemical reduction technique at ambient temperature and its characterization. Ferric chloride hexa-hydrate (FeCl3 · 6H2O) and sodium boro-hydrate (NaBH4) were used for synthesis of Fe3O4 nanoparticles at ambient temperature. The elemental composition of the synthesized Fe3O4 nanoparticles was determined by energy dispersive analysis of x-rays technique. The x-ray diffraction (XRD) technique was used for structural characterization of the nanoparticles. The crystallite size of the nanoparticles was determined using XRD data employing Scherrer’s formula and Hall-Williamson’s plot. Surface morphology of as-synthesized Fe3O4 nanoparticles was studied by scanning electron microscopy. High resolution transmission electron microscopy analysis of the as-synthesized Fe3O4 nanoparticles showed narrow range of particles size distribution. The optical absorption of the synthesized Fe3O4 nanoparticles was studied by UV-vis-NIR spectroscopy. The as-synthesized nanoparticles were analyzed by Fourier transform infrared spectroscopy technique for absorption band study in the infrared region. The magnetic properties of the as-synthesized Fe3O4 nanoparticles were evaluated by vibrating sample magnetometer technique. The thermal stability of the as-synthesized Fe3O4 nanoparticles was studied by thermogravimetric technique. The obtained results are elaborated and discussed in details in this paper.

  12. Preparation and property characterization of PAA/Fe3O4 nanocomposite

    Institute of Scientific and Technical Information of China (English)

    WEI Shanshan; ZHANG Yi; XU Jiarui

    2007-01-01

    PAA/Fe3O4 nanocomposites were prepared by mixing nano-Fe3O4 and polyacrylic acid(PAA)ethanol solution and then evaporating the solvent.The materials were characterized by transmission electron microscope(TEM),Fourier transform infrared spectroscope(FTIR),thermogravimetry analysis (TGA),dynamic ultra-micro hardness tester (DUMHT)and superconducting quantum interference device (SQUID)magnetometer.Results showed that PAA coordinated with nano-Fe3O4 to form a cross-linking structure.The presence of nano-Fe3O4 enhanced the thermal stability of the nanocomposite.The elasticity and hardness of the nanocomposite increased,and the indentation depth reduced with the increase of Fe3O4 content in the composites.The nanocomposites showed superparamagnetic properties at 300K.

  13. Preparation of MWCNT-Fe3O4 Nanocomposites from Iron Sand Using Sonochemical Route

    Science.gov (United States)

    Rahmawati, R.; Melati, A.; Taufiq, A.; Sunaryono; Diantoro, M.; Yuliarto, B.; Suyatman, S.; Nugraha, N.; Kurniadi, D.

    2017-05-01

    The composites of multi-walled carbon nanotube (MWCNT) and magnetite (Fe3O4) nanoparticles from iron sand were successfully prepared via the sonochemical route. In this experiment, the MWCNT-Fe3O4 nanocomposites were prepared with different compositions of MWCNT (0.01%, 0.02%, and 0.04%) with the constant composition of Fe3O4 particles. The characterizations were performed by means of X-Ray Diffractometry (XRD), Fourier Transform Infra-Red (FTIR) Spectrometer and Scanning Electron Microscopy (SEM) integrated with Energy Dispersive X-Ray (EDX). The XRD data analysis showed that the Fe3O4 crystallize in spinel structure in nanometric size. Furthermore, the crystallinity of the samples tended to reduce by increasing the MWCNT compositions. The SEM images showed that Fe3O4 tend to agglomerate in nanometric size. The FTIR spectra detected the functional groups of Fe-O bonding that showed the existence of Fe2+ and Fe3+. In the composites, the Fe3O4 nanoparticles were physically mixed with the MWCNTs constructing a unique structure. The as prepared MWCNT-Fe3O4 nanocomposites have the potential for bio-applications.

  14. Synergistic removal of Pb(II, Cd(II and humic acid by Fe3O4@mesoporous silica-graphene oxide composites.

    Directory of Open Access Journals (Sweden)

    Yilong Wang

    Full Text Available The synergistic adsorption of heavy metal ions and humic acid can be very challenging. This is largely because of their competitive adsorption onto most adsorbent materials. Hierarchically structured composites containing polyethylenimine-modified magnetic mesoporous silica and graphene oxide (MMSP-GO were here prepared to address this. Magnetic mesoporous silica microspheres were synthesized and functionalized with PEI molecules, providing many amine groups for chemical conjugation with the carboxyl groups on GO sheets and enhanced the affinity between the pollutants and the mesoporous silica. The features of the composites were characterized using TEM, SEM, TGA, DLS, and VSM measurements. Series adsorption results proved that this system was suitable for simultaneous and efficient removal of heavy metal ions and humic acid using MMSP-GO composites as adsorbents. The maximum adsorption capacities of MMSP-GO for Pb(II and Cd (II were 333 and 167 mg g(-1 caculated by Langmuir model, respectively. HA enhances adsorption of heavy metals by MMSP-GO composites due to their interactions in aqueous solutions. The underlying mechanism of synergistic adsorption of heavy metal ions and humic acid were discussed. MMSP-GO composites have shown promise for use as adsorbents in the simultaneous removal of heavy metals and humic acid in wastewater treatment processes.

  15. Synergistic removal of Pb(II), Cd(II) and humic acid by Fe3O4@mesoporous silica-graphene oxide composites.

    Science.gov (United States)

    Wang, Yilong; Liang, Song; Chen, Bingdi; Guo, Fangfang; Yu, Shuili; Tang, Yulin

    2013-01-01

    The synergistic adsorption of heavy metal ions and humic acid can be very challenging. This is largely because of their competitive adsorption onto most adsorbent materials. Hierarchically structured composites containing polyethylenimine-modified magnetic mesoporous silica and graphene oxide (MMSP-GO) were here prepared to address this. Magnetic mesoporous silica microspheres were synthesized and functionalized with PEI molecules, providing many amine groups for chemical conjugation with the carboxyl groups on GO sheets and enhanced the affinity between the pollutants and the mesoporous silica. The features of the composites were characterized using TEM, SEM, TGA, DLS, and VSM measurements. Series adsorption results proved that this system was suitable for simultaneous and efficient removal of heavy metal ions and humic acid using MMSP-GO composites as adsorbents. The maximum adsorption capacities of MMSP-GO for Pb(II) and Cd (II) were 333 and 167 mg g(-1) caculated by Langmuir model, respectively. HA enhances adsorption of heavy metals by MMSP-GO composites due to their interactions in aqueous solutions. The underlying mechanism of synergistic adsorption of heavy metal ions and humic acid were discussed. MMSP-GO composites have shown promise for use as adsorbents in the simultaneous removal of heavy metals and humic acid in wastewater treatment processes.

  16. Heterogeneous dimer peptide-conjugated polylysine dendrimer-Fe3O4 composite as a novel nanoscale molecular probe for early diagnosis and therapy in hepatocellular carcinoma

    Science.gov (United States)

    Shen, Jian-Min; Li, Xin-Xin; Fan, Lin-Lan; Zhou, Xing; Han, Ji-Min; Jia, Ming-Kang; Wu, Liang-Fan; Zhang, Xiao-Xue; Chen, Jing

    2017-01-01

    A novel nanoscale molecular probe is formulated in order to reduce toxicity and side effects of antitumor drug doxorubicin (DOX) in normal tissues and to enhance the detection sensitivity during early imaging diagnosis. The mechanism involves a specific targeting of Arg-Gly-Asp peptide (RGD)-GX1 heterogeneous dimer peptide-conjugated dendrigraft poly-l-lysine (DGL)–magnetic nanoparticle (MNP) composite by αvβ3-integrin/vasculature endothelium receptor-mediated synergetic effect. The physicochemical properties of the nanoprobe were characterized by using transmission electron microscope, Fourier transform infrared spectroscopy, X-ray diffraction, dynamic light scattering (DLS), and vibrating sample magnetometer. The average diameter of the resulting MNP–DGL–RGD-GX1–DOX nanoparticles (NPs) was ~150−160 nm by DLS under simulate physiological medium. In the present experimental system, the loading amount of DOX on NPs accounted for 414.4 mg/g for MNP–DGL–RGD-GX1–DOX. The results of cytotoxicity, flow cytometry, and cellular uptake consistently indicated that the MNP–DGL–RGD-GX1–DOX NPs were inclined to target HepG2 cells in selected three kinds of cells. In vitro exploration of molecular mechanism revealed that cell apoptosis was associated with the overexpression of Fas protein and the significant activation of caspase-3. In vivo magnetic resonance imaging and biodistribution study showed that the MNP–DGL–RGD-GX1–DOX formulation had high affinity to the tumor tissue, leading to more aggregation of NPs in the tumor. In vivo antitumor efficacy research verified that MNP–DGL–RGD-GX1–DOX NPs possessed significant antitumor activity and the tumor inhibitory rate reached 78.5%. These results suggested that NPs could be promising in application to early diagnosis and therapy in hepatocellular carcinoma as a specific nanoprobe. PMID:28243083

  17. Synthesis and characterization of plasmonic and magnetically separable Ag/AgCl-Bi2WO6@ Fe3O4@SiO2 core-shell composites for visible light-induced water detoxification.

    Science.gov (United States)

    Meng, Xiangchao; Zhang, Zisheng

    2017-01-01

    A magnetic photocatalyst composite (Ag/AgCl-Bi2WO6) was proposed and investigated. Magnetic Bi2WO6 was hydrothermally loaded onto silica-coated Fe3O4 which was synthesized by coprecipitation in addition to a modified Stöber process. Ag nanoparticles were then photoreduced on the surface of Bi2WO6. The prepared samples were characterized by X-ray diffraction, transmission electron microscopy, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, and ultraviolet-visible light diffuse reflectance spectroscopy. Magnetic properties were investigated using a superconducting quantum interface magnetometer, with samples exhibiting quasi-superparamagnetic behaviour. The visible light-induced photocatalytic activities were evaluated by degrading a model dye, RhB, as well as a colourless aromatic organic compound, phenol. Samples found to possess an excellent performance in terms of detoxification. Pathways and mechanisms for the photocatalytic degradation of organic compounds in the presence of Ag/AgCl-(M) Bi2WO6 were also investigated and proposed. Copyright © 2016. Published by Elsevier Inc.

  18. Determination of trace/ultratrace rare earth elements in environmental samples by ICP-MS after magnetic solid phase extraction with Fe3O4@SiO2@polyaniline-graphene oxide composite.

    Science.gov (United States)

    Su, Shaowei; Chen, Beibei; He, Man; Hu, Bin; Xiao, Zuowei

    2014-02-01

    A novel Fe3O4@SiO2@polyaniline-graphene oxide composite (MPANI-GO) was prepared through a simple noncovalent method and applied to magnetic solid phase extraction (MSPE) of trace rare earth elements (REEs) in tea leaves and environmental water samples followed by inductively coupled plasma mass spectrometry (ICP-MS) detection. The prepared MPANI-GO was characterized by transmission electron microscopy and vibrating sample magnetometer. Various parameters affecting MPANI-GO MSPE of REEs have been investigated. Under the optimized conditions, the limits of detection (LODs, 3σ) for REEs were in the range of 0.04-1.49 ng L(-1) and the relative standard deviations (RSDs, c=20 ng L(-1), n=7) were 1.7-6.5%. The accuracy of the proposed method was validated by analyzing a Certified Reference Material of GBW 07605 tea leaves. The method was also successfully applied for the determination of trace REEs in tea leaves and environmental water samples. The developed MPANI-GO MSPE-ICP-MS method has the advantages of simplicity, rapidity, high sensitivity, high enrichment factor and is suitable for the analysis of trace REEs in samples with complex matrix.

  19. Synthesis and characterization of ZnS@Fe3O4 fluorescent-magnetic bifunctional nanospheres

    Science.gov (United States)

    Koc, Kenan; Karakus, Baris; Rajar, Kausar; Alveroglu, Esra

    2017-10-01

    Herein, we synthesized and characterized fluorescent and super paramagnetic ZnS@Fe3O4 nanospheres. First, (3-mercaptopropyl) trimethoxysilane (MPS) capped ZnS quantum dots (QDs) and SiO2 coated Fe3O4 nanoparticles were synthesized separately by using solution growth and co-precipitation techniques. After synthesis and characterization of these two nanoparticles, they were conglutinated together in a nano sized sphere. The QDs were attached to the surface of the Fe3O4 nanoparticles by Sisbnd Osbnd Si bonds and so Sisbnd Osbnd Si bonds created a SiO2 network around the nanoparticles during the formation of the ZnS@Fe3O4 nanospheres. The synthesized MPS capped ZnS fluorescent QDs, SiO2 coated magnetite super paramagnetic nanoparticles and ZnS@Fe3O4 fluorescent-magnetic bifunctional nanospheres were characterized by using UV-Vis Absorption Spectroscopy, Fluorescence Spectroscopy, X-ray analysis, Vibrating Sample Magnetometer analysis, Attenuated Total Reflection-Fourier Transform Infrared Spectroscopy, Scanning Electron Microscope and Energy-dispersive X-ray spectroscopy. ZnS@Fe3O4 bifunctional nanospheres were shown to retain the magnetic properties of magnetite, while exhibiting the luminescent optical properties of ZnS nanoparticles. The combination of fluorescent and magnetic behaviors of nano composites make them useful for potential applications in the field of bio-medical and environmental.

  20. Incorporation of Fe3O4/CNTs nanocomposite in an epoxy coating for corrosion protection of carbon steel

    Science.gov (United States)

    Pham, Gia Vu; Truc Trinh, Anh; To, Thi Xuan Hang; Duong Nguyen, Thuy; Trang Nguyen, Thu; Hoan Nguyen, Xuan

    2014-09-01

    In this study Fe3O4/CNTs composite with magnetic property was prepared by attaching magnetic nanoparticles (Fe3O4) to carbon nanotubes (CNTs) by hydrothermal method. The obtained Fe3O4/CNTs composite was characterized by Fourier transform infrared (FTIR) spectroscopy, powder x-ray diffraction and transmission electron microscopy. The Fe3O4/CNTs composite was then incorporated into an epoxy coating at concentration of 3 wt%. Corrosion protection of epoxy coating containing Fe3O4/CNTs composite was evaluated by electrochemical impedance spectroscopy and adhesion measurement. The impedance measurements show that Fe3O4/CNTs composite enhanced the corrosion protection of epoxy coating. The corrosion resistance of the carbon steel coated by epoxy coating containing Fe3O4/CNTs composite was significantly higher than that of carbon steel coated by clear epoxy coating and epoxy coating containing CNTs. FE-SEM photographs of fracture surface of coatings showed good dispersion of Fe3O4/CNTs composite in the epoxy matrix.

  1. Preparation and adsorption properties of polycarboxylate nano-Fe3O4 magnetic composite particles%高分子聚羧酸-纳米Fe3O4磁性复合颗粒的制备及其对水中对羟基苯甲酸酯类化合物的吸附作用

    Institute of Scientific and Technical Information of China (English)

    沈昊宇; 赵永纲; 胡美琴; 夏清华

    2009-01-01

    采用悬浮聚合法制备高分子聚羧酸-纳米Fe3O4磁性复合颗粒(PC-NMPs).通过热重差热分析(TGA)、有机元素分析(EA)、原子吸收光谱(AAS)、X-射线衍射(XRD)、红外光谱(IR)、透射电镜(TEM)、振动样品磁强计(VSM)对合成的磁性复合颗粒进行了组成、结构、形貌、磁性等表征,并研究了其吸附和去除水中对羟基苯甲酸酯类化合物(Parabens)的性能.结果表明:合成的磁性复合颗粒平均粒径为100~150 nm,饱和磁化强度为10.66 emu/g,剩余磁化强度为0.61 emu/g,矫顽力为14.96 Oe;该磁性复合颗粒对4种常用的对羟基苯甲酸酯类化合物(Parabens)的等温吸附线基本符合Langmuir模式,对羟基苯甲酸甲酯(MPB)、对羟基苯甲酸乙酯(EPB)和对羟基苯甲酸丙酯(PPB)的饱和吸附量为556 mg/g;对羟基苯甲酸丁酯(BPB)的饱和吸附量为588mg/g.该复合颗粒能有效去除水中对羟基苯甲酸甲酯类化合物,是潜在的环境激素吸附剂和去除剂.该复合颗粒表面富含羧基可与Parabens类化合物形成氢键、苯环间存在π-π相互作用,有利于吸附过程快速有效地进行.

  2. Synthesis and characterizations of Fe3O4-acid fuchsin tagged poly(ɛ-caprolactone) nanocomposites

    Science.gov (United States)

    Meenarathi, Balakrishnan; Kannammal, Lingasamy; Palanikumar, Shanmugavel; Anbarasan, Ramasamy

    2014-04-01

    Ring opening polymerization (ROP) of caprolactone (CL) was carried out at different experimental conditions such as variation in [M], [M/I] and temperature under N2 atmosphere at 160 °C for 2 h with mild stirring condition by using acid fuchsin (AF) decorated Fe3O4 as a novel chemical initiator with the aid of stannous octoate as an effective catalyst. Thus, prepared polymer nano composite samples were characterised by various analytical techniques such as Fourier transform infrared (FTIR) spectroscopy, nuclear magnetic resonance (NMR) spectroscopy, UV-visible spectroscopy, fluorescence spectroscopy, differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), gel permeation chromatography (GPC), vibrating sample measurement (VSM), scanning electron microscopy (SEM) and field emission scanning electron microscopy (FESEM). Presence of Fe2p and Fe3p was confirmed by x-ray photoelectron spectroscopy (XPS) analysis. It was found that while increasing the [M/I] the melt transition values were increased. The surface catalytic effect of Fe3O4/AF hybrid system towards the ROP of CL was also studied.

  3. Polylactide-based polyurethane shape memory nanocomposites (Fe3O4/PLAUs) with fast magnetic responsiveness

    Science.gov (United States)

    Gu, Shu-Ying; Jin, Sheng-Peng; Gao, Xie-Feng; Mu, Jian

    2016-05-01

    Polylactide-based polyurethane shape memory nanocomposites (Fe3O4/PLAUs) with fast magnetic responsiveness are presented. For the purpose of fast response and homogeneous dispersion of magnetic nanoparticles, oleic acid was used to improve the dispersibility of Fe3O4 nanoparticles in a polymer matrix. A homogeneous distribution of Fe3O4 nanoparticles in the polymer matrix was obtained for nanocomposites with low Fe3O4 loading content. A small agglomeration was observed for nanocomposites with 6 wt% and 9 wt% loading content, leading to a small decline in the mechanical properties. PLAU and its nanocomposites have glass transition around 52 °C, which can be used as the triggering temperature. PLAU and its nanocomposites have shape fixity ratios above 99%, shape recovery ratios above 82% for the first cycle and shape recovery ratios above 91% for the second cycle. PLAU and its nanocomposites also exhibit a fast water bath or magnetic responsiveness. The magnetic recovery time decreases with an increase in the loading content of Fe3O4 nanoparticles due to an improvement in heating performance for increased weight percentage of fillers. The nanocomposites have fast responses in an alternating magnetic field and have potential application in biomedical areas such as intravascular stent.

  4. Fe3O4@Carbon Nanosheets for All-Solid-State Supercapacitor Electrodes.

    Science.gov (United States)

    Fan, Huailin; Niu, Ruiting; Duan, Jiaqi; Liu, Wei; Shen, Wenzhong

    2016-08-03

    Fe3O4@carbon nanosheet composites were synthesized using ammonium ferric citrate as the Fe3O4/carbon precursor and graphene oxide as the structure-directing agent under a hydrothermal process. The surface chemical compositions, pore structures, and morphology of the composite were analyzed and characterized by nitrogen adsorption isotherms, TG analysis, FT-IR, X-ray photoelectron energy spectrum, transmission electron microscopy, and scanning electron microscopy. The composites showed excellent specific capacitance of 586 F/g, 340 F/g at 0.5 A/g and 10 A/g. The all-solid-state asymmetric supercapacitor device assembled using carbon nanosheets in situ embedded Fe3O4 composite and porous carbon showed a largest energy density of 18.3 Wh/kg at power density of 351 W/kg in KOH/PVA gel electrolyte. The synergism of high special surface to volume ratio, mesoporous structure, graphene-based conduction paths, and Fe3O4 nanoparticles provided a high surface area of ion-accessibility, high electric conductivity, and the utmost utilization of Fe3O4 and resulted in excellent specific capacitance, outstanding rate capability and cycling life as all-solid-state supercapacitor electrodes.

  5. Reactively sputtered Fe3O4-based films for spintronics

    Institute of Scientific and Technical Information of China (English)

    Li Peng; Jin Chao; Mi Wen-Bo; Bai Hai-Li

    2013-01-01

    Half metallic polycrystalline,epitaxial Fe3O4 films and Fe3O4-based heterostructures for spintronics were fabricated by DC reactive magnetron sputtering.Large tunneling magnetoresistance was found in the polycrystalline Fe3O4 films and attributed to the insulating grain boundaries.The pinning effect of the moments at the grain boundaries leads to a significant exchange bias.Frozen interfacial/surface moments induce weak saturation of the high-field magnetoresistance.The films show a moment rotation related butterfly-shaped magnetoresistance.It was found that in the films,natural growth defects,antiphase boundaries,and magnetocrystaltine anisotropy play important roles in high-order anisotropic magnetoresistance.Spin injection from Fe3O4 films to semiconductive Si and ZnO was measured to be 45% and 28.5%,respectively.The positive magnetoresistance in the Fe3O4-based heterostructures is considered to be caused by a shift of the Fe3O4 eg ↑ band near the interface.Enhanced magnetization was observed in Fe3O4/BiFeO3 heterostructures experimentally and further proved by first principle calculations.The enhanced magnetization can be explained by spin moments of the thin BiFeO3 layer substantially reversing into a ferromagnetic arrangement under a strong coupling that is principally induced by electronic orbital reconstruction at the interface.

  6. Use of hydroxypropyl-β-cyclodextrin/polyethylene glycol 400, modified Fe3O4 nanoparticles for congo red removal.

    Science.gov (United States)

    Yu, Lan; Xue, Weihua; Cui, Lei; Xing, Wen; Cao, Xinli; Li, Hongyu

    2014-03-01

    Fe3O4 nanoparticles were modified with Hydroxypropyl-β-cyclodextrin (HP-β-CD) and Polyethylene glycol 400 (PEG400) by a facile one-pot homogeneous precipitation method, and were used as a novel nano-adsorbent for the removal of congo red (CR) from aqueous solutions. The polymer-modified composites were characterized by FTIR, TEM, TGA, XRD and VSM, and showed excellent adsorption efficiency for CR. The value of the maximum adsorption capacity calculated according to the Langmuir isotherm model were 1.895g/g, which are much high and about 19 times that of Fe3O4 nanoparticles. Desorption study further indicates the good regeneration ability of the nanocomposites. The results suggest that the HP-β-CD/PEG400-modified Fe3O4 nanoparticles is a promising adsorbent for CR removal from aqueous solutions, and it is easily recycled owing to its large specific surface area and unique magnetic responsiveness. Crown Copyright © 2013. Published by Elsevier B.V. All rights reserved.

  7. Microwave absorption property of aligned MWCNT/Fe3O4

    Science.gov (United States)

    Hekmatara, H.; Seifi, M.; Forooraghi, K.

    2013-11-01

    This study investigated the microwave absorption properties of magnetic modified multiwall carbon nanotubes (MWCNTs) with different alignments to the electric field (E vector) of the incident electromagnetic (EM) waves. MWCNTs were decorated with Fe3O4 nanoparticles using the wet chemical method and the resulting MWCNT/Fe3O4 was then used as a filler in a MWCNT/Fe3O4/epoxy resin composite at different weight-to-epoxy-resin ratios (2%, 5%, and 8%) with good uniformity and alignment. For each filler concentration, three samples were produced with different alignments of carbon nanotubes using the solution-casting method. For sample one, the nanotube axis (k) was parallel to the E vector of the EM wave, for sample two, k was perpendicular to E, and the third sample contained randomly oriented nanotubes. Magnetic MWCNTs were exposed to a 0.4 T magnetic field in the desired direction to achieve the desired alignment of carbon nanotubes in epoxy resin. Microwave absorption characterization of the considered ranging band (X-band) at all concentrations where the alignment of MWCNT/Fe3O4 was parallel to the incident E vector showed increased absorption. Samples with a perpendicular alignment of MWCNT/Fe3O4 to incident E had the lowest absorption. Samples containing 2 wt% and 8 wt% MWCNT/Fe3O4 aligned parallel to E and had reflection losses exceeding 14.4 dB and 23.6 dB, respectively, over a 10-11 GHz range. The 5 wt% parallel aligned MWCNT/Fe3O4 showed an absorbing peak of 27 dB and a bandwidth broadened to 1.2 GHz.

  8. Synthesis and characterization of Fe3O4@ZnS and Fe3O4@Au@ZnS core-shell nanoparticles

    Science.gov (United States)

    Stefan, M.; Leostean, C.; Pana, O.; Soran, M.-L.; Suciu, R. C.; Gautron, E.; Chauvet, O.

    2014-01-01

    In the present work we report new assets on the synthesis and characterization of magnetite based core-shell nanoparticles such as Fe3O4@ZnS and Fe3O4@Au@ZnS. The composites were prepared by seed mediated growth which consist in a sequential growth of a second or third component on a preformed magnetite seeds in the presence of sodium laurylsulphate additives with essential role in growth and aggregation of nanoparticles. Evolved gas analysis (EGA) coupled with FT-IR was used in order to evidence the stages of ZnS shell formation. XRD studies were used for the structural characterization while high resolution transmission electron microscopy gave information concerning morphology and size distributions of nanoparticles. Qualitative and quantitative compositional analysis of samples was made by X-ray photoelectron spectroscopy (XPS). All the samples showed magnetic response due to the superparamagnetic behavior of magnetite cores. Increased saturation magnetization was determined for Fe3O4@ZnS samples. A significant photoluminescence (PL) enhancement was also observed as a result of Fe3O4:Zn2+ molar ratio decrease. Additional PL increased response was realized by inserting a gold shell between the magnetite core and ZnS outer shell. Considerations regarding both PL and magnetization enhancements are also presented.

  9. A Facile and Green Synthetic Route for Preparation of Heterostructure Fe3O4@Au Nanocomposites

    Directory of Open Access Journals (Sweden)

    Xie Liping

    2017-01-01

    Full Text Available Magnetic nanoparticles offer many exciting opportunities in biology and biomedicine, such as magnetic resonance imaging, magnetic hyperthermia therapy, biomedical diagnosis. The synthesis of multifunctional magnetic nanocomposites that possess water-solubility, magnetic properties and optical stability by a green method at room temperature in aqueous phase is still an unmet need. Here, we developed a simple and green method for preparing Fe3O4@Au integrated the super-paramagnetic and optical properties by seed-mediated growth at mild condition in aqueous phase. The amphiphilic, non-ionic and nontoxic polymer poly(vinylpyrrolidone (PVP was used as a coupling agent for synthesis of Fe3O4@Au nanocomposites, which avoided the direct connection of Au and Fe3O4, and improved the saturation magnetization values of Fe3O4@Au to 40 emu/g at room temperature. We anticipate that the multifunctional Fe3O4@Au nanocomposites with high magnetic and good optical properties will provide a platform for potential diagnostic and therapeutic biomedical applications.

  10. Facile self-assembly of Fe3O4 nanoparticles@WS2 nanosheets: A promising candidate for supercapacitor electrode

    Science.gov (United States)

    Dai, Yu; Wu, Xiao; Sha, Dawei; Chen, Ming; Zou, Han; Ren, Jie; Wang, Jingjing; Yan, Xuehua

    2016-10-01

    Graphene-like dichalcogenides with huge surface area and nanostructured transition metal oxides with extraordinarily high theoretical capacities could be composited as promising electrode candidates for supercapacitors. In this work, monolayer and few-layers WS2 nanosheets were exfoliated by combination of ball-milling and sonication. A facile strategy for the hierarchical self-assembly of Fe3O4 nanoparticles (Fe3O4NPs) on WS2 nanosheets was developed to synthesize Fe3O4NPs@WS2 nanocomposites via hydrothermal method. Fe3O4NPs are uniformly dispersed on the WS2 nanosheets without aggregation. The particle size of Fe3O4NPs is about 3 nm. The nanocomposite shows strong enhancements of electrochemical behaviors. This self-assembly synthesis strategy may have great prospects for other 0D/2D nanocomposites in supercapacitors and other energy devices. [Figure not available: see fulltext.

  11. The sandwich-type electrochemiluminescence immunosensor for α-fetoprotein based on enrichment by Fe3O4-Au magnetic nano probes and signal amplification by CdS-Au composite nanoparticles labeled anti-AFP.

    Science.gov (United States)

    Zhou, Hankun; Gan, Ning; Li, Tianhua; Cao, Yuting; Zeng, Saolin; Zheng, Lei; Guo, Zhiyong

    2012-10-09

    A novel and sensitive sandwich-type electrochemiluminescence (ECL) immunosensor was fabricated on a glassy carbon electrode (GCE) for ultra trace levels of α-fetoprotein (AFP) based on sandwich immunoreaction strategy by enrichment using magnetic capture probes and quantum dots coated with Au shell (CdS-Au) as the signal tag. The capture probe was prepared by immobilizing the primary antibody of AFP (Ab1) on the core/shell Fe(3)O(4)-Au nanoparticles, which was first employed to capture AFP antigens to form Fe(3)O(4)-Au/Ab1/AFP complex from the serum after incubation. The product can be separated from the background solution through the magnetic separation. Then the CdS-Au labeled secondary antibody (Ab2) as signal tag (CdS-Au/Ab2) was conjugated successfully with Fe(3)O(4)-Au/Ab1/AFP complex to form a sandwich-type immunocomplex (Fe(3)O(4)-Au/Ab1/AFP/Ab2/CdS-Au), which can be further separated by an external magnetic field and produce ECL signals at a fixed voltage. The signal was proportional to a certain concentration range of AFP for quantification. Thus, an easy-to-use immunosensor with magnetic probes and a quantum dots signal tag was obtained. The immunosensor performed at a level of high sensitivity and a broad concentration range for AFP between 0.0005 and 5.0 ng mL(-1) with a detection limit of 0.2 pg mL(-1). The use of magnetic probes was combined with pre-concentration and separation for trace levels of tumor markers in the serum. Due to the amplification of the signal tag, the immunosensor is highly sensitive, which can offer great promise for rapid, simple, selective and cost-effective detection of effective biomonitoring for clinical application.

  12. Surface Organic Modification of Fe3O4 Magnetic Nanoparticles

    Institute of Scientific and Technical Information of China (English)

    CUI Sheng; SHEN Xiaodong; LIN Benlan; JIANG Guodong; ZHANG Weihua

    2008-01-01

    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.

  13. Synthesis and properties of hybrid hydroxyapatite-ferrite (Fe3O4) particles for hyperthermia applications

    Science.gov (United States)

    Tkachenko, M. V.; Kamzin, A. S.

    2016-04-01

    Hybrid ceramics consisting of hydroxyapatite Ca10(PO4)6(OH)2 and ferrite Fe3O4 were synthesized using a two-stage procedure. The first stage included the synthesis of Fe3O4 ferrite particles by co-precipitation and the synthesis of hydroxyapatite. In the second stage, the magnetic hybrid hydroxyapatite-ferrite bioceramics were synthesized by a thorough mixing of the obtained powders of carbonated hydroxyapatite and Fe3O4 ferrite taken in a certain proportion, pressing into tablets, and annealing in a carbon dioxide atmosphere for 30 min at a temperature of 1200°C. The properties of the components and hybrid particles were investigated using X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and Mössbauer spectroscopy. The saturation magnetization of the hybrid ceramic composite containing 20 wt % Fe3O4 was found to be 12 emu/g. The hybrid hydroxyapatite (Ca10(PO4)6(OH)2)-ferrite Fe3O4 ceramics, which are promising for the use in magnetotransport and hyperthermia treatment, were synthesized and investigated for the first time.

  14. Magnetically Recyclable Fe3O4@His@Cu Nanocatalyst for Degradation of Azo Dyes.

    Science.gov (United States)

    Kurtan, U; Amir, Md; Baykal, A; Sözeri, H; Toprak, M S

    2016-03-01

    Fe3O4@His@Cu magnetic recyclable nanocatalyst (MRCs) was synthesized by reflux method using L-histidine as linker. The composition, structure and magnetic property of the product were characterized by X-ray powder diffraction (XRD), Scanning electron microscopy (SEM), Fourier Transform infrared spectroscopy (FT-IR) and vibrating sample magnetometry (VSM). Powder XRD, FT-IR and EDAX results confirmed that the as-synthesized products has Fe3O4 with spinel structure and Cu nanoparticles with moderate crystallinity without any other impurities. The surface of the Fe3O4@His nanocomposite was covered by tiny Cu nanoparticles. We examine the catalytic activity of Fe3O4@His@Cu MRCs for the degradation of two azo dyes, methyl orange (MO) and methylene blue (MB) as well as their mixture. The reusability of the nanocatalyst was good and sustained even after 3 cycles. Therefore this innovated Fe3O4@His@Cu MRCs has a potential to be used for purification of waste water.

  15. Synthesis, Characterization, and Adsorptive Properties of Fe3O4/GO Nanocomposites for Antimony Removal

    Directory of Open Access Journals (Sweden)

    Xiuzhen Yang

    2017-01-01

    Full Text Available A magnetic Fe3O4/GO composite with potential for rapid solid-liquid separation through a magnetic field was synthesized using GO (graphene oxide and Fe3O4 (ferriferous oxide. Characterization of Fe3O4/GO used scanning electron microscope (SEM, X-ray diffractometer (XRD, Fourier transform infrared spectrometer (FT-IR, and Vibrating Sample Magnetometer (VSM. A number of factors such as pH and coexisting ions on adsorbent dose were tested in a series of batch experiments. The results showed that GO and Fe3O4 are strongly integrated. For pH values in the range of 3.0~9.0, the removal efficiency of Sb(III using the synthesized Fe3O4/GO remained high (95%. The adsorption showed good fit to a pseudo-second-order and Langmiur model, with the maximum adsorption capacity of 9.59 mg/g maintained across pH 3.0–9.0. Thermodynamic parameters revealed that the adsorption process was spontaneous and endothermic. Analysis by X-ray photoelectron spectroscopy (XPS showed that the adsorption process is accompanied by a redox reaction.

  16. Nanoparticle size matters in the formation of plasma protein coronas on Fe3O4 nanoparticles.

    Science.gov (United States)

    Hu, Zhengyan; Zhang, Hongyan; Zhang, Yi; Wu, Ren'an; Zou, Hanfa

    2014-09-01

    When nanoparticles (NPs) enter into biological systems, proteins would interact with NPs to form the protein corona that can critically impact the biological identity of the nanomaterial. Owing to their fundamental scientific interest and potential applications, Fe3O4 NPs of different sizes have been developed for applications in cell separation and protein separation and as contrast agents in magnetic resonance imaging (MRI), etc. Here, we investigated whether nanoparticle size affects the formation of protein coronas around Fe3O4 NPs. Both the identification and quantification results demonstrated that particle size does play an important role in the formation of plasma protein coronas on Fe3O4 NPs; it not only influenced the protein composition of the formed plasma protein corona but also affected the abundances of the plasma proteins within the coronas. Understanding the different binding profiles of human plasma proteins on Fe3O4 NPs of different sizes would facilitate the exploration of the bio-distributions and biological fates of Fe3O4 NPs in biological systems.

  17. In situ anchor of magnetic Fe3O4 nanoparticles onto natural maifanite as efficient heterogeneous Fenton-like catalyst

    Science.gov (United States)

    Zhao, Hang; Weng, Ling; Cui, Wei-Wei; Zhang, Xiao-Rui; Xu, Huan-Yan; Liu, Li-Zhu

    2016-09-01

    In situ anchor of magnetic Fe3O4 nanoparticles (NPs) onto the surface of natural maifanite was realized by chemical oxidation coprecipitation in hot alkaline solution. The Fe3O4/maifanite composites were characterized by XRD, FTIR, SEM, and TEM. These results indicated that polycrystalline Fe3O4 NPs with inverse spinel structure were formed and tightly dispersed on maifanite surface. Based on the measurement of surface Zeta potential of maifanite at different medium pHs, the possible combination mechanism between natural maifanite and Fe3O4 NPs was proposed. Then, the asobtained composites were developed as highly efficient heterogeneous Fenton-like catalyst for the discoloration of an azo dye, Methyl Orange (MO). The comparative tests on MO discoloration in different systems revealed that Fe3O4/maifanite composite exhibited much higher Fenton-like catalytic activity than Fe3O4 NPs and the heterogeneous Fentonlike reaction governed the discoloration of MO. Kinetic results clearly showed that MO discoloration process followed the second-order kinetic model. Fe3O4/maifanite composites exhibited the typical ferromagnetic property detected by VSM and could be easily separated from solution by an external magnetic field.

  18. Electrostatic Self-Assembly of Fe3O4 Nanoparticles on Graphene Oxides for High Capacity Lithium-Ion Battery Anodes

    Directory of Open Access Journals (Sweden)

    Jung Kyoo Lee

    2013-09-01

    Full Text Available Magnetite, Fe3O4, is a promising anode material for lithium ion batteries due to its high theoretical capacity (924 mA h g−1, high density, low cost and low toxicity. However, its application as high capacity anodes is still hampered by poor cycling performance. To stabilize the cycling performance of Fe3O4 nanoparticles, composites comprising Fe3O4 nanoparticles and graphene sheets (GS were fabricated. The Fe3O4/GS composite disks of mm dimensions were prepared by electrostatic self-assembly between negatively charged graphene oxide (GO sheets and positively charged Fe3O4-APTMS [Fe3O4 grafted with (3-aminopropyltrimethoxysilane (APTMS] in an acidic solution (pH = 2 followed by in situ chemical reduction. Thus prepared Fe3O4/GS composite showed an excellent rate capability as well as much enhanced cycling stability compared with Fe3O4 electrode. The superior electrochemical responses of Fe3O4/GS composite disks assure the advantages of: (1 electrostatic self-assembly between high storage-capacity materials with GO; and (2 incorporation of GS in the Fe3O4/GS composite for high capacity lithium-ion battery application.

  19. Catalytic Oxidation of Phenol and 2,4-Dichlorophenol by Using Horseradish Peroxidase Immobilized on Graphene Oxide/Fe3O4

    Directory of Open Access Journals (Sweden)

    Qing Chang

    2016-08-01

    Full Text Available Graphene oxide/Fe3O4 (GO/Fe3O4 nanoparticles were synthesized by an ultrasonic-assisted reverse co-precipitation method, and then horseradish peroxidase (HRP was covalently immobilized onto GO/Fe3O4 with 1-ethyl-3-(3-dimethyaminopropylcarbodiimide (EDC as a cross-linking agent. In order to enhance the phenol removal efficiency and prevent the inactivation of the enzyme, the polyethylene glycol with highly hydrophilicity was added in this reaction, because the adsorption capacity for the polymer by degradation was stronger than the HRP. The results showed that the immobilized enzyme removed over 95% of phenol from aqueous solution. The catalytic condition was extensively optimized among the range of pH, mass ratio of PEG/phenol as well as initial concentration of immobilized enzyme and H2O2. The HRP immobilized on GO/Fe3O4 composite could be easily separated under a magnetic field from the reaction solution and reused.

  20. Solvothermal synthesis of magnetic Fe3O4 microparticles via self-assembly of Fe3O4 nanoparticles

    Institute of Scientific and Technical Information of China (English)

    Wei Zhang; Fenglei Shen; Ruoyu Hong

    2011-01-01

    Ferromagnetic Fe3O4 nanoparticles were synthesized and then self-assembled into microparticles via a solvothermal method, using FeCI3.6H2O as the iron source, sodium oleate as the surfactant, and ethylene glycol as the reducing agent and solvent. The obtained Fe3O4 microparticles were characterized by X-ray powder diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy and vibrating sample magnetometer (VSM). The size and morphology of the particles were examined using transmission electron microscopy (TEM) and scanning electron microscopy (SEM). The Fe3O4 microparticles of nearly monodisperse diameters, controllable in the range of 120-400 nm, consist of assemblies of Fe3O4nanoparticles with a diameter of 22 nm. The effects of reaction time, amount of surfactant and NaAc on the products were discussed. Interestingly, by using the pre-synthesized Fe3O4 microparticles as the growth substrates, spherical and smooth-looking Fe3O4 microparticles with average diameter of lμmwere obtained. A plausible formation process was discussed.

  1. Magnetically separable and recyclable Fe3O4-polydopamine hybrid hollow microsphere for highly efficient peroxidase mimetic catalysts.

    Science.gov (United States)

    Liu, Shujun; Fu, Jianwei; Wang, Minghuan; Yan, Ya; Xin, Qianqian; Cai, Lu; Xu, Qun

    2016-05-01

    Magnetic Fe3O4-polydopamine (PDA) hybrid hollow microspheres, in which Fe3O4 nanoparticles were firmly incorporated in the cross-linked PDA shell, have been prepared through the formation of core/shell PS/Fe3O4-PDA composites based on template-induced covalent assembly method, followed by core removal in a tetrahydrofuran solution. The morphology, composition, thermal property and magnetic property of the magnetic hybrid hollow microspheres were characterized by SEM, TEM, FT-IR, XRD, TGA, and vibrating sample magnetometer, respectively. Results revealed that the magnetic hybrid hollow microspheres had about 380 nm of inner diameter and about 30 nm of shell thickness, and 13.6 emu g(-1) of magnetization saturation. More importantly, the Fe3O4-PDA hybrid hollow microspheres exhibited intrinsic peroxidase-like activity, as they could quickly catalyze the oxidation of typical substrates 3,3',5,5'-tetramethylbenzidine (TMB) in the presence of hydrogen peroxide. Compared with PDA/Fe3O4 composites where Fe3O4 nanoparticles were loaded on the surface of PDA microspheres, the stability of Fe3O4-PDA hybrid hollow microspheres was greatly improved. As-prepared magnetic hollow microspheres might open up a new application field in biodetection, biocatalysis, and environmental monitoring. Copyright © 2016 Elsevier Inc. All rights reserved.

  2. Fast defluorination and removal of norfloxacin by alginate/Fe@Fe3O4 core/shell structured nanoparticles.

    Science.gov (United States)

    Niu, Hongyun; Dizhang; Meng, Zhaofu; Cai, Yaqi

    2012-08-15

    Alginate-Fe(2+)/Fe(3+) polymer coated Fe(3)O(4) magnetic nanoparticles (Fe(3)O(4)@ALG/Fe MNPs) with core/shell structure are prepared and used as heterogeneous Fenton nanocatalyst to degrade norfloxacin (NOF). The Fenton-like process based on Fe(3)O(4)@ALG/Fe shows much higher efficiency on NOF degradation. Compared with Fe(3)O(4) nanoparticle-H(2)O(2) system, NOF degradation in Fe(3)O(4)@AlG/Fe-H(2)O(2) system can be conducted in a wide pH range (pH 3.5-6.5) and independent on temperature. With 0.98 mM H(2)O(2) and 0.4 g L(-1) Fe(3)O(4)@ALG/Fe, 100% of NOF and 90% of TOC is removed within 60 min, and the fluorine element in NOF molecule changes into F(-) ions within 1 min, indicating that NOF degradation in this Fenton-like reaction is performed through direct defluorination pathway. XPS analysis shows that TOC removal in reaction solution mainly results from the adsorption of NOF degradation intermediates on catalyst. Due to the paramagneticity and high saturation magnetization of Fe(3)O(4)@ALG/Fe, the used catalyst with adsorbed NOF intermediate is collected from aqueous solution by applying an external magnetic field, leading to complete removal of NOF from water samples. As being composed of inorganic materials and biopolymer, Fe(3)O(4)@ALG/Fe MNPs are robust, thermo-stable, nontoxic and environmentally friendly. These attractive features endow Fe(3)O(4)@ALG/Fe as a potent Fenton-like catalyst for fluoroquinolones degradation. Copyright © 2012 Elsevier B.V. All rights reserved.

  3. Photocatalytic Bactericidal Efficiency of Ag Doped TiO2/Fe3O4 on Fish Pathogens under Visible Light

    Directory of Open Access Journals (Sweden)

    Ekkachai Kanchanatip

    2014-01-01

    Full Text Available This research evaluates photocatalytic bactericidal efficiencies of Ag-TiO2/Fe3O4 in visible light using target pollutants that include Aeromonas hydrophila, Edwardsiella tarda, and Photobacterium damselae subsp. piscicida. The investigation started with Ag-TiO2/Fe3O4 synthesis and calcination followed by a series of product tests that include the examination of crystallite phase, light absorption, element composition morphology, and magnetic properties. The results of the experiment indicate that Ag and Fe3O4 significantly enhanced the light absorption capacity of TiO2 in the entire visible light range. The Ag-TiO2/Fe3O4 prepared in this study displays significantly enhanced visible light absorption and narrowed band gap energy. The magnetic property of Ag-TiO2/Fe3O4 made it easy for retrieval using a permanent magnet bar. The photocatalytic activity of Ag-TiO2/Fe3O4 remains above 85% after three application cycles, which indicates high and favorable efficiency in bactericidal evaluation. The experiments have proved that the Ag-TiO2/Fe3O4 magnetic photocatalyst is a promising photocatalyst for antibacterial application under visible light.

  4. Facile Preparation, Characterization, and Highly Effective Microwave Absorption Performance of CNTs/Fe3O4/PANI Nanocomposites

    Directory of Open Access Journals (Sweden)

    Deqing Zhang

    2013-01-01

    Full Text Available A facile method has been developed to synthesize light-weight CNTs/Fe3O4/PANI nanocomposites. The formation route was proposed as the coprecipitation of Fe2+ and Fe3+ and an additional process of in situ polymerization of aniline monomer. The structure and morphology of CNTs/Fe3O4/PANI were characterized by transmission electron microscopy (TEM, X-ray photoelectron spectroscopy (XPS, and Fourier transform infrared (FTIR spectroscopy. The TEM investigation shows that the CNTs/Fe3O4/PANI nanocomposites exhibit less intertwined structure and that many more Fe3O4 particles are attached homogeneously on the surface of CNTs, indicating that PANI can indeed help CNTs to disperse in isolated form. The wave-absorbing properties were investigated in a frequency of 2–18 GHz. The results show that the CNTs/Fe3O4/PANI nanocomposites exhibit a super absorbing behavior and possess a maximum reflection loss of −48 dB at 12.9 GHz, and the bandwidth below −20 dB is more than 5 GHz. More importantly, the absorption peak frequency ranges of the CNTs/Fe3O4/PANI composites can be tuned easily by changing the wax weight ratio and thickness of CNTs/Fe3O4/PANI paraffin wax matrix.

  5. Synthesis of Fe3O4 nanoparticles by wet milling iron powder in a planetary ball mill

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Fe3O4 nanoparticles with sizes ranging from 30 to 80nm were synthesized by wet milling iron powders in a planetary ball mill. The phase composition and the morphologies of the as-synthesized products were measured by X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Nanosized Fe3O4 particles were prepared by wet milling metallic iron powder (-200 mesh, 99%)rotation speed of 300 rpm. The use of the iron balls in this method played a key role in Fe3O4 formation. The present technique is simple and the process is easy to carry out.

  6. Synthesis and microwave absorption enhancement of graphene@Fe3O4@SiO2@NiO nanosheet hierarchical structures.

    Science.gov (United States)

    Wang, Lei; Huang, Ying; Sun, Xu; Huang, Haijian; Liu, Panbo; Zong, Meng; Wang, Yan

    2014-03-21

    Hierarchical structures of graphene@Fe3O4@SiO2@NiO nanosheets were prepared by combining the versatile sol-gel process with a hydrothermal reaction. Graphene@Fe3O4 composites were first synthesized by the reduction reaction between FeCl3 and diethylene glycol (DEG) in the presence of GO. Then, graphene@Fe3O4 was coated with SiO2 to obtain graphene@Fe3O4@SiO2. Finally, NiO nanosheets were grown perpendicularly on the surface of graphene@Fe3O4@SiO2 and graphene@Fe3O4@SiO2@NiO nanosheet hierarchical structures were formed. Moreover, the microwave absorption properties of both graphene@Fe3O4 and graphene@Fe3O4@SiO2@NiO nanosheets were investigated between 2 and 18 GHz microwave frequency bands. The electromagnetic data demonstrate that graphene@Fe3O4@SiO2@NiO nanosheet hierarchical structures exhibit significantly enhanced microwave absorption properties compared with graphene@Fe3O4, which probably originate from the unique hierarchical structure with a large surface area and high porosity.

  7. Ultrasonic irradiation-driven sonocatalytic degradation of methylene blue by ternary Fe3O4/ZnO/NGP nanocomposites

    Science.gov (United States)

    Harno, Faurul Fitri; Taufik, Ardiansyah; Saleh, Rosari

    2017-01-01

    In the current work, ZnO nanoparticles were modified by Fe3O4 and nanographene platelets (NGP) to enhance their sonocatalytic activity for degradation of methylene blue. The molar ratio between Fe3O4 and ZnO is 1:5, so we denote it as Fe3O4/5ZnO Ternary Fe3O4/5ZnO/NGP with various wt.% of nanographene platelets were fabricated by the sol-gel combining with the hydrothermal methods. The structure, chemical composition and surface area of ternary Fe3O4/5ZnO/NGP were investigated by X-ray diffraction (XRD), energy dispersive X-ray (EDX) and surface area analyzer while the thermal properties were characterized by Thermogravimetric Analysis (TGA) measurements. The magnetic properties of the samples were investigated using vibrating sample magnetometer (VSM). The conditions such as the weight ratio of nanographene platelets in ternary Fe3O4/5ZnO/NGP, catalyst dose and reusability of catalyst were investigated to identify the degradation of methylene blue under ultrasonic irradiation. A possible mechanism was proposed for the degradation of methylene blue over ternary Fe3O4/5ZnO-nanographene platelets ultrasonic irradiation. The ternary Fe3O4/5ZnO-nanographene platelets can be separated from the system effectively and easily using external magnet field. A significant sonocatalytic activity after four successive recycles was recorded and confirmed that the structure of ternary Fe3O4/5ZnO-nanographene platelets is stable during the sonocatalytic process.

  8. Texture induced magnetic anisotropy in Fe3O4 films

    Science.gov (United States)

    Liu, Er; Huang, Zhaocong; Zheng, Jian-Guo; Yue, Jinjin; Chen, Leyi; Wu, Xiumei; Sui, Yunxia; Zhai, Ya; Tang, Shaolong; Du, Jun; Zhai, Hongru

    2015-10-01

    This letter reports a free energy density model for textured films in which the related physical concept and expression of magneto-texture anisotropy energy are presented. The structural characterization and out-of-plane angular dependence ferromagnetic resonance of strongly textured Fe3O4 films were systematically investigated. We found that the typical free energy density model for polycrystalline film cannot be applied to the textured films. With the introduction of magneto-texture anisotropy energy in the free energy density model for thin films, we simulated and quantitatively determined the competing anisotropies in (111)-textured Fe3O4 films.

  9. Biocompatibility of magnetic Fe3O4 nanoparticles and their cytotoxic effect on MCF-7 cells

    Directory of Open Access Journals (Sweden)

    Chen DZ

    2012-09-01

    Full Text Available Daozhen Chen,1,3,* Qiusha Tang,2,* Xiangdong Li,3,* Xiaojin Zhou,1 Jia Zang,1 Wen-qun Xue,1 Jing-ying Xiang,1 Cai-qin Guo11Central Laboratory, Wuxi Hospital for Matemaland Child Health Care Affiliated Medical School of Nanjing, Jiangsu Province; 2Department of Pathology and Pathophysiology, Medical College, Southeast University, Jiangsu Province; 3The People’s Hospital of Aheqi County, Xinjiang, China *These authors contributed equally to this workBackground: The objective of this study was to evaluate the synthesis and biocompatibility of Fe3O4 nanoparticles and investigate their therapeutic effects when combined with magnetic fluid hyperthermia on cultured MCF-7 cancer cells.Methods: Magnetic Fe3O4 nanoparticles were prepared using a coprecipitation method. The appearance, structure, phase composition, functional groups, surface charge, magnetic susceptibility, and release in vitro were characterized by transmission electron microscopy, x-ray diffraction, scanning electron microscopy-energy dispersive x-ray spectroscopy, and a vibrating sample magnetometer. Blood toxicity, in vitro toxicity, and genotoxicity were investigated. Therapeutic effects were evaluated by MTT [3-(4, 5-dimethyl-2-thiazolyl-2, 5-diphenyl-2H-tetrazolium bromide] and flow cytometry assays.Results: Transmission electron microscopy revealed that the shapes of the Fe3O4 nanoparticles were approximately spherical, with diameters of about 26.1 ± 5.2 nm. Only the spinel phase was indicated in a comparison of the x-ray diffraction data with Joint Corporation of Powder Diffraction Standards (JCPDS X-ray powder diffraction files. The O-to-Fe ratio of the Fe3O4 was determined by scanning electron microscopy-energy dispersive x-ray spectroscopy elemental analysis, and approximated pure Fe3O4. The vibrating sample magnetometer hysteresis loop suggested that the Fe3O4 nanoparticles were superparamagnetic at room temperature. MTT experiments showed that the toxicity of the material

  10. Photodegradation of Methylene Blue by TiO2-Fe3O4-Bentonite Magnetic Nanocomposite

    Directory of Open Access Journals (Sweden)

    Wei Chen

    2015-01-01

    Full Text Available Fe3O4-bentonite nanoparticles have been prepared by a coprecipitation technique under a nitrogen atmosphere. An aqueous suspension of bentonite was first modified with FeCl2 and FeCl3. TiO2 was then loaded onto the surface of the Fe3O4-bentonite by a sol-gel method. After sufficient drying, the colloidal solution was placed in a muffle furnace at 773 K to obtain the TiO2-Fe3O4-bentonite composite. The material has been characterized by scanning electron microscopy (SEM, X-ray diffraction (XRD analysis, and vibrating sample magnetometry (VSM. Morphological observation showed that Fe3O4 and TiO2 nanoparticles had been adsorbed on the surface of bentonite nanoneedles. The material was then applied for the photodegradation of the azo dye methylene blue (MB. It was found that the removal efficiency of MB exceeded 90% under UV illumination, and that only a 20% mass loss was incurred after six cycles. The composite material thus showed good photocatalytic performance and recycling properties.

  11. Fabrication of graphene oxide decorated with Fe3O4@SiO2 for immobilization of cellulase

    Science.gov (United States)

    Li, Yue; Wang, Xiang-Yu; Jiang, Xiao-Ping; Ye, Jing-Jing; Zhang, Ye-Wang; Zhang, Xiao-Yun

    2015-01-01

    Fe3O4@SiO2-graphene oxide (GO) composites were successfully fabricated by chemical binding of functional Fe3O4@SiO2 and GO and applied to immobilization of cellulase via covalent attachment. The prepared composites were further characterized by transmission electron microscopy and Fourier transform infrared spectroscopy. Fe3O4 nanoparticles (NPs) were monodisperse spheres with a mean diameter of 17 ± 0.2 nm. The thickness of SiO2 layer was calculated as being 6.5 ± 0.2 nm. The size of Fe3O4@SiO2 NPs was 24 ± 0.3 nm, similar to that of Fe3O4@SiO2-NH2. Fe3O4@SiO2-GO composites were synthesized by linking of Fe3O4@SiO2-NH2 NPs to GO with the catalysis of EDC and NHS. The prepared composites were used for immobilization of cellulase. A high immobilization yield and efficiency of above 90 % were obtained after the optimization. The half-life of immobilized cellulase (722 min) was 3.34-fold higher than that of free enzyme (216 min) at 50 °C. Compared with the free cellulase, the optimal temperature of the immobilized enzyme was not changed; but the optimal pH was shifted from 5.0 to 4.0, and the thermal stability was enhanced. The immobilized cellulase could be easily separated and reused under magnetic field. These results strongly indicate that the cellulase immobilized onto the Fe3O4@SiO2-GO composite has potential applications in the production of bioethanol.

  12. Surface Modfication of Fe3O4 Nanoparticles

    Institute of Scientific and Technical Information of China (English)

    LIU Yong-jian; JIA Hong-yi; ZHUANG Hong

    2006-01-01

    Nanometer particles are important portion of magnetic fluid. Fe3O4 magnetic nanoparticles were studied in this paper and the surface modification of Fe3O4 nanoparticles was investigated by a series of experiments. Fe3O4 magnetic nanoparticles were synthesized with pH value, temperature, and the dosage of surfactant. The phase, structure, size and magnetism of nanoparticles were tested by X-ray diffration (XRD), transmission electron microscopy (TEM) and magnetic balance. On the basis of the surface modification coating mechanism, the experimental phenomena and the effects on the variation of size, magnetism and stability of Fe3O4 nanoparticles were theoretically analyzed. X-Ray diffraction spectrum and TEM photograph show that 1) the nanoparticles structure is perfect, 2) the diameter of namoparticles is small and have good deliquescence, and 3) Sodium oleate is the anion surfactant. Therefore 1) the good condition of surface modification is in an acidic solution, 2) the best temperature of surface modification is at 80 ℃, and 3) the dosage of surfactant should be about 0.6 times of that of Fe2+.

  13. Removal mechanism of selenite by Fe3O4-precipitated mesoporous magnetic carbon microspheres.

    Science.gov (United States)

    Lu, Jianwei; Fu, Fenglian; Ding, Zecong; Li, Na; Tang, Bing

    2017-05-15

    A mesoporous composite of magnetic carbon microspheres (MCMSs) was synthesized via introducing Fe3O4 nanoscale particles to the surface of carbon microspheres (CMSs) by coprecipitation. Scanning electron microscopy and transmission electron microscopy showed the Fe3O4 nanoscale particles were dispersedly immobilized on the surface of CMSs. The MCMSs demonstrated effective removal of selenite (Se(IV)) from wastewater. MCMSs showed the regular pattern where the lower pH value, the lower residual Se(IV) concentration. The coexisting sulfate, nitrate, chloride, carbonate, and silicate had no significant effect on Se(IV) removal, whereas phosphate hindered the removal of Se(IV) by competing with Se(IV) and formed inner-sphere complexes with Fe3O4 on the surface of MCMSs. Through X-ray photoelectron spectroscopy analysis, Se(IV) can not only form inner-sphere complexes with MCMSs, but also be reduced to insoluble elemental selenium (Se(0)) by Fe3O4 which was oxidized and formed γ-Fe2O3. Moreover, the superparamagnetic MCMSs can be easily separated from solution by means of an external magnetic field. The high removal efficiency for Se(IV) and rapid separability of MCMSs made them promising materials for the application in the practice. Copyright © 2017 Elsevier B.V. All rights reserved.

  14. Heteroepitaxy of Fe3O4/Muscovite: A New Perspective for Flexible Spintronics.

    Science.gov (United States)

    Wu, Ping-Chun; Chen, Ping-Fan; Do, Thi Hien; Hsieh, Ying-Hui; Ma, Chun-Hao; Ha, Thai Duy; Wu, Kun-Hong; Wang, Yu-Jia; Li, Hao-Bo; Chen, Yi-Chun; Juang, Jenh-Yih; Yu, Pu; Eng, Lukas M; Chang, Chun-Fu; Chiu, Po-Wen; Tjeng, Liu Hao; Chu, Ying-Hao

    2016-12-14

    Spintronics has captured a lot of attention since it was proposed. It has been triggering numerous research groups to make their efforts on pursuing spin-related electronic devices. Recently, flexible and wearable devices are in a high demand due to their outstanding potential in practical applications. In order to introduce spintronics into the realm of flexible devices, we demonstrate that it is feasible to grow epitaxial Fe3O4 film, a promising candidate for realizing spintronic devices based on tunneling magnetoresistance, on flexible muscovite. In this study, the heteroepitaxy of Fe3O4/muscovite is characterized by X-ray diffraction, high-resolution transmission electron microscopy, and Raman spectroscopy. The chemical composition and magnetic feature are investigated by a combination of X-ray photoelectron spectroscopy and X-ray magnetic circular dichroism. The electrical and magnetic properties are examined to show the preservation of the primitive properties of Fe3O4. Furthermore, various bending tests are performed to show the tunability of functionalities and to confirm that the heterostructures retain the physical properties under repeated cycles. These results illustrate that the Fe3O4/muscovite heterostructure can be a potential candidate for the applications in flexible spintronics.

  15. Multifunctional polypyrrole@fe3o4 nanoparticles for dual-modal imaging and in vivo photothermal cancer therapy

    KAUST Repository

    Tian, Qiwei

    2013-11-27

    Magnetic Fe3O4 crystals are produced in situ on preformed polypyrrole (PPY) nanoparticles by rationally converting the residual Fe species in the synthetic system. The obtained PPY@Fe3O4 composite nanoparticles exhibit good photostability and biocompatibility, and they can be used as multifunctional probes for MRI, thermal imaging, and photothermal ablation of cancer cells. © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  16. Fe3O4 nanoparticles on graphene oxide sheets for isolation and ultrasensitive amperometric detection of cancer biomarker proteins.

    Science.gov (United States)

    Sharafeldin, Mohamed; Bishop, Gregory W; Bhakta, Snehasis; El-Sawy, Abdelhamid; Suib, Steven L; Rusling, James F

    2017-05-15

    Ultrasensitive mediator-free electrochemical detection for biomarker proteins was achieved at low cost using a novel composite of Fe3O4 nanoparticles loaded onto graphene oxide (GO) nano-sheets (Fe3O4@GO). This paramagnetic Fe3O4@GO composite (1µm size range) was decorated with antibodies against prostate specific antigen (PSA) and prostate specific membrane antigen (PSMA), and then used to first capture these biomarkers and then deliver them to an 8-sensor detection chamber of a microfluidic immunoarray. Screen-printed carbon sensors coated with electrochemically reduced graphene oxide (ERGO) and a second set of antibodies selectively capture the biomarker-laden Fe3O4@GO particles, which subsequently catalyze hydrogen peroxide reduction to detect PSA and PSMA. Accuracy was confirmed by good correlation between patient serum assays and enzyme-linked immuno-sorbent assays (ELISA). Excellent detection limits (LOD) of 15 fg/mL for PSA and 4.8 fg/mL for PSMA were achieved in serum. The LOD for PSA was 1000-fold better than the only previous report of PSA detection using Fe3O4. Dynamic ranges were easily tunable for concentration ranges encountered in serum samples by adjusting the Fe3O4@GO Concentration. Reagent cost was only $0.85 for a single 2-protein assay.

  17. Preparation and Electromagnetic Wave-absorbing Properties of Micro-polyaniline/Fe3 O4 Hollow Spheres%微米聚苯胺/Fe3 O4空心球的制备及吸波性能

    Institute of Scientific and Technical Information of China (English)

    李涛; 张龙; 陈颖; 郭亚军; 杜雪岩

    2015-01-01

    采用界面聚合和Pickering乳液聚合相结合的方法,以甲苯为软模板,磁性Fe3 O4纳米颗粒为稳定剂,十二烷基苯磺酸钠( SDBS)为乳化剂,过硫酸铵( APS)为氧化剂,盐酸( HCl)为掺杂剂,制备了掺杂态聚苯胺/Fe3O4(D-PANI/Fe3O4)空心球.作为比较,在不掺杂盐酸的条件下,制备了本征态聚苯胺/Fe3O4(PANI/Fe3 O4)空心球.用透射电子显微镜( TEM)、扫描电子显微镜( SEM)、X射线衍射( XRD)仪、傅里叶变换红外光谱( FTIR)仪、热重分析( TG)仪、振动样品磁强( VSM)计及恒压四探针测试仪对复合材料的形貌、结构、组成和电磁性能进行了表征.结果表明, D-PANI/Fe3 O4空心球的直径约为2.8μm,电导率和饱和磁化强度(Ms)分别为2.75×10-2 S/cm 和54.26 A·m2/kg.用矢量网络分析(VNA)仪对 D-PANI/Fe3O4空心球和PANI/Fe3 O4空心球吸波性能进行分析,结果表明, D-PANI/Fe3 O4空心球在12.64 GHz处的最小反射率为-43.3 dB,对应的匹配厚度为2 mm,其吸波性能明显优于PANI/Fe3 O4空心球.%Doped polyaniline/Fe3 O4( D-PANI/Fe3 O4 ) with hollow spheres were prepared by the combination of interfacial polymerization and Pickering emulsion polymerization method with toluene as soft template, Fe3 O4 nanoparticles as cosurfactant, sodium dodecyl benzene sulfonate( SDBS) as emulsifier, ammonium per-sulfate ( APS ) as oxidant, hydrochloric acid ( HCl ) as the doping agent. And as a comparison, the polyaniline/Fe3 O4 ( PANI/Fe3 O4 ) with hollow spheres were prepared without acid doping. The morphology, structure, integrant, magnetic and electrical properties of the composite material were characterized by trans-mission electron microscopy( TEM) , scanning electron microscopy( SEM) , X-ray diffraction( XRD) , Fourier transform infrared spectroscopy( FTIR) , thermogravimetric( TG) , vibration sample magnetism( VSM) and the four-probe method, respectively. The results indicate that the D-PANI/Fe3 O4 with hollow spheres structures

  18. Factors Influence the Structural and Magnetic Properties of Ag-Fe3O4 Nanocomposites Synthesized by Reduction Method

    Science.gov (United States)

    Fajaroh, F.; Nazriati

    2017-05-01

    Silver nanoparticles integrated with a magnetic matrix such as Fe3O4 to form Ag-Fe3O4 nanocomposites show some advantages in their applications as an antibacterial agent and heterogeneous catalyst. This material can be synthesized by a combination of electrochemical and reduction methods supported by ultrasonic route. The purposes of this study are to synthesize the nanocomposites by reduction method and to study the effect of synthesis parameters on the structural and magnetic properties of the generated nanocomposites. This research consisted of three main stages. The first step was the electrochemical synthesis of magnetite nanoparticles using electro-oxidation of iron in water. Second, adsorption of Ag+ on the surface of Fe3O4 carried out by sonication of a mixture of AgNO3 solution and powder of Fe3O4 nanoparticles. The third stage was the reduction of Ag+ to Ag0 with glucose as reductant and NaOH as an accelerator, where it was conducted under a variation of AgNO3 mole ratios to glucose and NaOH concentration. The characterizations of Ag-Fe3O4 nanocomposites were performed using XRD and VSM. The results of the characterizations showed that Ag-Fe3O4 nanocomposites have been successfully synthesized. There was an optimum concentration of NaOH at pH (11) and mole ratio of AgNO3 to glucose (1 : 8) in the synthesis process producing the composite with the highest crystallinity.

  19. Kinetics of Fe3O4 formation by air oxidation

    Institute of Scientific and Technical Information of China (English)

    杨喜云; 龚竹青; 刘丰良

    2004-01-01

    The kinetics of Fe3O4 formation by air oxidation of slightly acidic suspension of Fe(OH)2 was studied. The effects of initial concentration of Fe(Ⅱ), temperature, partial pressure of oxygen, air flow rate and stirring rate on the oxidation rate were investigated. The results show that Fe3O4 formation is composed of two-step reaction, the first step is the formation of Fe(OH)+2 by oxidation of Fe(OH)+ complex ions, the second step is the formation of magnetite by dehydration and deprotonation of Fe(OH)+ and Fe(OH)+2. The oxidation reaction is zero-order with respect to the concentration of Fe(Ⅱ) and around 0.5-order with respect to partial pressure of oxygen, and oxygen transfer process is rate-limiting step of oxidation reaction with apparent activation energy of 2.74 kJ·mol-1.

  20. Large tunneling magnetoresistance in octahedral Fe3O4 nanoparticles

    OpenAIRE

    Arijit Mitra; Barun Barick; Jeotikanta Mohapatra; Sharma, H.; Meena, S. S.; ASLAM, M.

    2016-01-01

    We have observed large tunneling Magnetoresistance (TMR) in amine functionalized octahedral nanoparticle assemblies. Amine monolayer on the surface of nanoparticles acts as an insulating barrier between the semimetal Fe3O4 nanoparticles and provides multiple tunnel junctions where inter-granular tunneling is plausible. The tunneling magnetoresistance recorded at room temperature is 38% which increases to 69% at 180 K. When the temperature drops below 150 K, coulomb staircase is observed in th...

  1. Local probing of magnetoelectric properties of PVDF/Fe3O4 electrospun nanofibers by piezoresponse force microscopy

    Science.gov (United States)

    Zheng, Tian; Yue, Zhilian; Wallace, Gordon G.; Du, Yi; Martins, Pedro; Lanceros-Mendez, Senentxu; Higgins, Michael J.

    2017-02-01

    The coupling of magnetic and electric properties in polymer-based magnetoelectric composites offers new opportunities to develop contactless electrodes, effectively without electrical connections, for less-invasive integration into devices such as energy harvesters, sensors, wearable and implantable electrodes. Understanding the macroscale-to-nanoscale conversion of the properties is important, as nanostructured and nanoscale magnetoelectric structures are increasingly fabricated. However, whilst the magnetoelectric effect at the macroscale is well established both theoretically and experimentally, it remains unclear how this effect translates to the nanoscale, or vice versa. Here, PVDF/Fe3O4 polymer-based composite nanofibers are fabricated using electrospinning to investigate their piezoelectric and magnetoelectric properties at the single nanofiber level.

  2. Synthesis, characterization and electrical properties of Fe3O4/poly(vinyl alcohol-co-acrylic acid) nanocomposites

    Science.gov (United States)

    P, Jayakrishnan; Ramesan, M. T.

    2014-10-01

    This work focused on the synthesis of magnetite (Fe3O4)/poly(vinyl alcohol-co-acrylic acid) nanocomposite by in situ polymerization. The composite were characterized by FT-IR spectroscopy, XRD, SEM, TGA, AC and DC conductivity measurements. The spectroscopic studies revealed the molecular interaction between the polymer and nanocomposites. SEM, XRD indicated the uniform dispersion of nanoparticle inside the molecular chain of copolymer. TGA studies indicated the excellent thermal stability of copolymer nanocomposites. AC and DC conductivity of nanocomposites were higher than that of the copolymer and conductivity values were significantly increased with increase in concentration of metal oxide nanoparticles. These properties suggest that the polymer composite can be used as multifunctional material for nanoelectronics.

  3. Deposition and Magnetic Properties of Fe3O4/Fe/Fe3O4Tri-layer Films

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    The Fe3O4/Fe/Fe3O4 (MIM) tri-layer films (200 nm/12~93 nm/200 nm) were prepared on Si(100) by DC-magnetron reactive-sputtering followed by air- or vacuum-annealing at 280~400℃ for 1.5 h, respectively. Magnetic properties and phases under different sandwich and annealing conditions were studied. In MIM structure, the incorporation of the interlayer iron does increase the magnetization measured under 8 kOe (M8K), but reduce coercivity (Hc). The Hc of as deposited films decreases from 354 Oe to 74 Oe; while M8K increases from 254 to 392 emu/cc. By annealing in air, the whole MIM tri-layer film becomes γ-Fe2Oa, Hc is about 550 Oe and M8K is around 250 emu/cc. The coercivity mechanism of as-deposited and annealed MIM tri layer films belongs to domain-wall pinning type. δM plots show that when the interlayer Fe thickness is 12 nm, the Fe and Fe3O4 layers are decoupled in the as-deposited and annealed states; while it is coupled in the as deposited state when the Fe thickness increases to 23 nm. Vacuum annealing of the MIM films leads to increase in both coercivity and magnetization, and to enhance the exchange coupling between layers.

  4. Synthesis and photocatalytic properties of Fe3O4@TiO2 core-shell for degradation of Rhodamine B

    Science.gov (United States)

    Mufti, Nandang; Munfarriha, Ulfatien; Fuad, Abdulloh; Diantoro, Markus

    2016-02-01

    The aim of this research is to synthesis Fe3O4@TiO2 core-shell and used it as photocatalytic for degradation of Rhodamine B. The Fe3O4 nanoparticle core was synthesized by coprecipitation method from the iron sand. The TiO2 shell synthesized using coprecipitation method to capsulated Fe3O4 nanoparticle with vary of Fe3O4 mass. The Fe3O4@TiO2 core-shells were characterized using SEM-EDX, XRD. Photocatalytic activity of Rhodamine B degradation was performed under UV irradiation with variation of time exposure. The efficiency of photodegradation is measured by UV-Vis spectrophotometer. The XRD result showed that Fe3O4 nanoparticle is single phase with crystal size of 15.5 nm. The existence of Fe3O4 and anatase of TiO2 phases in the XRD pattern shows that The Fe3O4@TiO2 core-shells are successfully synthesized. While, the TiO2 shell is confirmed by thermal test up to 550 OC for two hours to the samples. Based on SEM characterization, The Fe3O4@TiO2 core-shells are agglomerated with averages diameter sizes of particles between 38.5 nm to 72.8 nm. The concentration of TiO2 decrease with increasing Fe3O4 mass with atomic composition of Fe/Ti elements in Fe3O4@TiO2 core-shells are 0.083, 1.12, and 1.48. Based on photo degradation test of Rhodamine B under UV irradiation, we conclude that the degradation of Rhodamin B is caused by absorbsion and photocatalytic mechanism. For photocatalytic mechanism the efficiency of photodegradation of Rhodamin B increases by increasing TiO2 concentration.

  5. Formation and characterization of β-cyclodextrin (β-CD) - polyethyleneglycol (PEG) - polyethyleneimine (PEI) coated Fe3O4 nanoparticles for loading and releasing 5-Fluorouracil drug.

    Science.gov (United States)

    Prabha, G; Raj, V

    2016-05-01

    In this work, β-cyclodextrin (β-CD) - polyethyleneglycol (PEG) - polyethyleneimine (PEI) coated iron oxide nanoparticles (Fe3O4-β-CD-PEG-PEI) were developed as drug carriers for drug delivery applications. The 5- Fluorouracil (5-FU) was chosen as model drug molecule. The developed nanoparticles (Fe3O4-β-CD-PEG-PEI) were characterized by various techniques such as Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), Scanning electron microscopy (SEM), transmission electron microscopy (TEM) and vibrating sample magnetometry (VSM). The average particles size range of 5-FU loaded Fe3O4-β-CD, Fe3O4-β-CD-PEG and Fe3O4-β-CD-PEG-PEI nanoparticles were from 151 to 300nm and zeta potential value of nanoparticles were from -43mV to -20mV as measured using Malvern Zetasizer. Finally, encapsulation efficiency (EE), loading capacity (LC) and in-vitro drug release performance of 5-FU drug loaded Fe3O4-β-CD, Fe3O4-β-CD-PEG and Fe3O4-β-CD-PEG-PEI nanoparticles was evaluated by UV-vis spectroscopy. In-vitro cytotoxicity tests investigated by MTT assay indicate that 5-FU loaded Fe3O4-β-CD-PEG-PEI nanoparticles were toxic to cancer cells and non-toxic to normal cells. The in-vitro release behavior of 5-FU from drug (5-FU) loaded Fe3O4-β-CD-PEG-PEI composite at different pH values and temperature was studied. It was found that 5-FU was released faster in pH 6.8 than in the acidic mediums (pH 1.2), and the released quantity was higher. Therefore, the newly prepared Fe3O4-β-CD-PEG-PEI carrier exhibits a promising potential capability for anticancer drug delivery in tumor therapy.

  6. [Adsorption of methylene blue from aqueous solution onto magnetic Fe3O4/ graphene oxide nanoparticles].

    Science.gov (United States)

    Chang, Qing; Jiang, Guo-Dong; Hu, Meng-Xuan; Huang, Jia; Tang, He-Qing

    2014-05-01

    A simple ultrasound-assisted co-precipitation method was developed to prepare magnetic Fe3O4/graphene oxide (Fe3O4/ GO) nanoparticles. The characterization with transmission electron microscope (TEM) indicated that the products possessed small particle size. The hysteresis loop of the dried Fe3O4/GO nanoparticles demonstrated that the sample had typical features of superparamagnetic material. Batch adsorption studies were carried out to investigate the effects of the initial pH of the solution, the dosage of adsorbent, the contact time and temperature on the adsorption of methylene blue. The results indicated that the composites prepared could be used over a broad pH range (pH 6-9). The adsorption process was very fast within the first 25 min and the equilibrium was reached at 180 min. The adsorption equilibrium and kinetics data fitted well with the Langmuir isotherm model and the pseudo-second-order kinetic model. The adsorption process was a spontaneous and endothermic process in nature. The composite exhibited fairly high adsorption capacity (196.5 mg.g-1) of methylene blue at 313 K. In addition, the magnetic composite could be effectively and simply separated by using an external magnetic field, and then regenerated by hydrogen peroxide and recycled for further use. The results indicated that the adsorbent had a potential in the application of the dye wastewater treatment.

  7. One-step thermolysis synthesis of two-dimensional ultrafine Fe3O4 particles/carbon nanonetworks for high-performance lithium-ion batteries

    Science.gov (United States)

    Zhang, Wanqun; Li, Xiaona; Liang, Jianwen; Tang, Kaibin; Zhu, Yongchun; Qian, Yitai

    2016-02-01

    To tackle the issue of inferior cycle stability and rate capability for Fe3O4 anode materials in lithium ion batteries, ultrafine Fe3O4 nanocrystals uniformly encapsulated in two-dimensional (2D) carbon nanonetworks have been fabricated through thermolysis of a simple, low-cost iron(iii) acetylacetonate without any extra processes. Moreover, compared to the reported Fe3O4/carbon composites, the particle size of Fe3O4 is controllable and held down to ~3 nm. Benefitting from the synergistic effects of the excellent electroconductive carbon nanonetworks and uniform distribution of ultrafine Fe3O4 particles, the prepared 2D Fe3O4/carbon nanonetwork anode exhibits high reversible capacity, excellent rate capability and superior cyclability. A high capacity of 1534 mA h g-1 is achieved at a 1 C rate and is maintained without decay up to 500 cycles (1 C = 1 A g-1). Even at the high current density of 5 C and 10 C, the 2D Fe3O4/carbon nanonetworks maintain a reversible capacity of 845 and 647 mA h g-1 after 500 discharge/charge cycles, respectively. In comparison with other reported Fe3O4-based anodes, the 2D Fe3O4/carbon nanonetwork electrode is one of the most attractive of those in energy storage applications.To tackle the issue of inferior cycle stability and rate capability for Fe3O4 anode materials in lithium ion batteries, ultrafine Fe3O4 nanocrystals uniformly encapsulated in two-dimensional (2D) carbon nanonetworks have been fabricated through thermolysis of a simple, low-cost iron(iii) acetylacetonate without any extra processes. Moreover, compared to the reported Fe3O4/carbon composites, the particle size of Fe3O4 is controllable and held down to ~3 nm. Benefitting from the synergistic effects of the excellent electroconductive carbon nanonetworks and uniform distribution of ultrafine Fe3O4 particles, the prepared 2D Fe3O4/carbon nanonetwork anode exhibits high reversible capacity, excellent rate capability and superior cyclability. A high capacity of 1534 mA h

  8. Fabrication and Electromagnetic Properties of Conjugated NH2-CuPc@Fe3O4

    Science.gov (United States)

    Yan, Liang; Pu, Zejun; Xu, Mingzhen; Wei, Renbo; Liu, Xiaobo

    2017-10-01

    Conjugated amino-phthalocyanine copper containing carboxyl groups/magnetite (NH2-CuPc@Fe3O4) has been fabricated from FeCl3·6H2O and NH2-CuPc via a simple solvothermal method and its electromagnetic properties investigated. Scanning electron microscopy and transmission electron microscopy revealed that the NH2-CuPc@Fe3O4 was a waxberry-like nanomaterial with NH2-CuPc molecules effectively embedded in the interior of Fe3O4 particles in the form of beads. Introduction of NH2-CuPc effectively improved the complementarity between the dielectric and magnetic losses of the system, resulting in excellent electromagnetic performance. The minimum reflection loss of the as-prepared composite reached -33.4 dB at 7.0 GHz for coating layer thickness of 4.0 mm and bandwidth below -10.0 dB (90% absorption) of up to 3.8 GHz. These results indicate that introduction of NH2-CuPc results in a composite with potential for use as an electromagnetic microwave absorption material.

  9. Synthesis and characterization of Fe3O4-TiO2 core-shell nanoparticles

    Science.gov (United States)

    Stefan, M.; Pana, O.; Leostean, C.; Bele, C.; Silipas, D.; Senila, M.; Gautron, E.

    2014-09-01

    Composite core-shell nanoparticles may have morpho-structural, magnetic, and optical (photoluminescence (PL)) properties different from each of the components considered separately. The properties of Fe3O4-TiO2 nanoparticles can be controlled by adjusting the titania amount (shell thinness). Core-shell nanoparticles were prepared by seed mediated growth of semiconductor (TiO2) through a modified sol-gel process onto preformed magnetite (Fe3O4) cores resulted from the co-precipitation method. The structure and morphology of samples were characterized by X-ray diffraction, transmission electron microscopy (TEM), and high resolution-TEM respectively. X-ray photoelectron spectroscopy was correlated with ICP-AES. Magnetic measurements, optical absorption spectra, as well as PL spectroscopy indicate the presence of a charge/spin transfer from the conduction band of magnetite into the band gap of titania nanocrystals. The process modifies both Fe3O4 and TiO2 magnetic and optical properties, respectively.

  10. Tailoring the nickel nanoparticles anchored on the surface of Fe3O4@SiO2 spheres for nanocatalysis

    Science.gov (United States)

    Ding, Lei; Zhang, Min; Zhang, Yanwei; Yang, Jinbo; Zheng, Jing; Hayat, Tasawar; Alharbi, Njud S.; Xu, Jingli

    2017-08-01

    Herein, we report an efficient and universal strategy for synthesizing a unique triple-shell structured Fe3O4@SiO2@C-Ni hybrid composite. Firstly, the Fe3O4 cores were synthesized by hydrothermal reaction, and sequentially coated with SiO2 and a thin layer of nickel-ion-doped resin-formaldehyde (RF-Ni2+) using an extended Stöber method. This was followed by carbonization to produce the Fe3O4@SiO2@C-Ni nanocomposites with metallic nickel nanoparticles embedded in an RF-derived thin graphic carbon layer. Interestingly, the thin SiO2 spacer layer between RF-Ni2+ and Fe3O4 plays a critical role on adjusting the size and density of the nickel nanoparticles on the surface of Fe3O4@SiO2 nanospheres. The detailed tailoring mechanism is explicitly discussed, and it is shown that the iron oxide core can react with the nickel nanoparticles without the SiO2 spacer layer, and the size and density of the nickel nanoparticles can be effectively controlled when the SiO2 layer exits. The multifunctional composites exhibit a significantly enhanced catalytic performance in the reduction of 4-nitrophenol (4-NP).

  11. 纳米Fe3O4/凹凸棒石的制备及其吸波性能研究%Characterization and Microwave Absorbing Property of Fe3O4-Attapulgite Nanocomposites

    Institute of Scientific and Technical Information of China (English)

    胡吉祥; 张学斌; 桂和仁; 丁辉; 万泽林; 赫丽华; 王智勇; 凤仪

    2016-01-01

    The Fe3O4-attapulgite (Fe3O4-ATP) composite material was fabricated by a co-precipitation method and characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), high-resolution transmission electron microscopy (HRTEM) and vector network analyzer. XRD and XPS characterized the phase of as-prepared sample and the oxidation state of iron bearing minerals, respectively. The HRTEM images revealed that the Fe3O4 magnetic parricles grew on the surface of the ATP needles which diameter distributes from 10 nm to 80 nm. The microwave absorption capacity of Fe3O4-ATP was measured in the frequency range of 2~18 GHz by a vector network analyzer. It can be seen that the optimal relfection loss (RL) of all the samples with different thickness are more than -13 dB and the biggest relfection loss (RL) could be about -28 dB at 12.6 GHz with a layer thickness of 3.5 mm. The results indicated that the ATP-Fe3O4 exhibited good microwave absorption capacity and could be used as a new type of absorber.%通过化学共沉积法制备纳米Fe3O4/凹凸棒石复合粉体,并采用XRD、XPS、HRTEM和矢量网络分析仪等手段对其微结构和吸波性能进行表征和分析。XRD和XPS分别证明了复合粉体的物相和铁的氧化价态。 HRTEM图像显示,Fe3O4磁性粒子均匀分布在凹凸棒石黏土表面,颗粒尺寸为10~80 nm。使用矢量网络分析仪在2~18 GHz范围测试不同厚度的Fe3O4/凹凸棒石的反射率。结果显示,不同厚度样品的峰值均超过-13 dB,其中厚度为3.5 mm的样品在12.6 GHz处反射峰为-28 dB,说明Fe3O4/凹凸棒石具有优良的吸波性能,有望成为一种新型的吸波材料。

  12. Coupling Hollow Fe3O4-Fe Nanoparticles with Graphene Sheets for High-Performance Electromagnetic Wave Absorbing Material.

    Science.gov (United States)

    Qu, Bin; Zhu, Chunling; Li, Chunyan; Zhang, Xitian; Chen, Yujin

    2016-02-17

    We developed a strategy for coupling hollow Fe3O4-Fe nanoparticles with graphene sheets for high-performance electromagnetic wave absorbing material. The hollow Fe3O4-Fe nanoparticles with average diameter and shell thickness of 20 and 8 nm, respectively, were uniformly anchored on the graphene sheets without obvious aggregation. The minimal reflection loss RL values of the composite could reach -30 dB at the absorber thickness ranging from 2.0 to 5.0 mm, greatly superior to the solid Fe3O4-Fe/G composite and most magnetic EM wave absorbing materials recently reported. Moreover, the addition amount of the composite into paraffin matrix was only 18 wt %.

  13. Antifungal activity of multifunctional Fe 3O 4-Ag nanocolloids

    Science.gov (United States)

    Chudasama, Bhupendra; Vala, Anjana K.; Andhariya, Nidhi; Upadhyay, R. V.; Mehta, R. V.

    2011-05-01

    In recent years, rapid increase has been observed in the population of microbes that are resistant to conventionally used antibiotics. Antifungal drug therapy is no exception and now resistance to many of the antifungal agents in use has emerged. Therefore, there is an inevitable and urgent medical need for antibiotics with novel antimicrobial mechanisms. Aspergillus glaucus is the potential cause of fatal brain infections and hypersensitivity pneumonitis in immunocompromised patients and leads to death despite aggressive multidrug antifungal therapy. In the present article, we describe the antifungal activity of multifunctional core-shell Fe 3O 4-Ag nanocolloids against A. glaucus isolates. Controlled experiments are also carried out with Ag nanocolloids in order to understand the role of core (Fe 3O 4) in the antifungal action. The minimum inhibitory concentration (MIC) of nanocolloids is determined by the micro-dilution method. MIC of A. glaucus is 2000 μg/mL. The result is quite promising and requires further investigations in order to develop a treatment methodology against this death causing fungus in immunocompromised patients.

  14. Large tunneling magnetoresistance in octahedral Fe3O4 nanoparticles

    Directory of Open Access Journals (Sweden)

    Arijit Mitra

    2016-05-01

    Full Text Available We have observed large tunneling Magnetoresistance (TMR in amine functionalized octahedral nanoparticle assemblies. Amine monolayer on the surface of nanoparticles acts as an insulating barrier between the semimetal Fe3O4 nanoparticles and provides multiple tunnel junctions where inter-granular tunneling is plausible. The tunneling magnetoresistance recorded at room temperature is 38% which increases to 69% at 180 K. When the temperature drops below 150 K, coulomb staircase is observed in the current versus voltage characteristics as the charging energy exceeds the thermal energy. A similar study is also carried out with spherical nanoparticles. A 24% TMR is recorded at room temperature which increases to 41% at 180 K for spherical particles. Mössbauer spectra reveal better stoichiometry for octahedral particles which is attainable due to lesser surface disorder and strong amine coupling at the facets of octahedral Fe3O4 nanoparticles. Less stoichiometric defect in octahedral nanoparticles leads to a higher value of spin polarization and therefore larger TMR in octahedral nanoparticles.

  15. La-EDTA coated Fe3O4 nanomaterial: Preparation and application in removal of phosphate from water

    Institute of Scientific and Technical Information of China (English)

    Jiao Yang; Qingru Zeng; Liang Peng; Ming Lei; Huijuan Song; Boqing Tie; Jidong Gu

    2013-01-01

    La-EDTA-Fe3O4 was prepared by a chemical co-precipitation method.The magnetic composite was characterized by transmission electron microscopy (TEM),X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FT-IR).Furthermore,the adsorption properties of La-EDTA-Fe3O4 toward phosphate in water were investigated.The uptake rate of phosphate in water by La-EDTA-Fe3O4was 3-1000 times than that of EDTA-Fe3O4,and reached 97.8% at 7 hr.The adsorption process agreed well with the Freundlich model and kinetics studies showed that the adsorption of phosphate proceeds according to pseudo second-order adsorption kinetics.The maximum removal rate was achieved at pH 6.0-7.0.The La-EDTA-Fe3O4 had good adsorption properties and could be separated well from aqueous solution by a permanent magnet.Therefore,this nanomaterial has potential application for the removal of phosphate from large water bodies.

  16. Fabrication of Bi-Fe3O4@RGO hybrids and their catalytic performance for the reduction of 4-nitrophenol

    Science.gov (United States)

    Wang, Xuefang; Xia, Fengling; Li, Xichuan; Xu, Xiaoyang; Wang, Huan; Yang, Nian; Gao, Jianping

    2015-11-01

    Nanocatalysts are frequently connected to magnetic nanoparticles. These composites are easy to be retrieved from the reaction system under a magnetic field because of their magnetic properties. Magnetic separation is particularly promising in industry since it can solve many issues present in filtration, centrifugation, or gravitation separation. Herein, a facile method to prepare bismuth and Fe3O4 nanoparticles loaded on reduced graphene oxide magnetic hybrids (Bi-Fe3O4@RGO) using soluble starch as a dispersant is demonstrated. The magnetic Fe3O4 nanoparticles were synthesized by the co-precipitation of Fe2+ and Fe3+ ions, and Bi nanoparticles were fabricated by the redox reactions between sodium borohydride and ammonium bismuth citrate in the presence of soluble starch. Transmission electron microscopy images demonstrate that the average diameter of the Fe3O4 nanoparticles is about 5 nm and the diameters of Bi nanoparticles range from 10 to 20 nm. The magnetic Bi-Fe3O4@RGO hybrids exhibit high catalytic activity in the reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP) by NaBH4 with a first-order rate constant (K) of 0.00808 s-1 and is magnetically recyclable for at least five cycles. This strategy provides an efficient and recyclable catalyst for the use in environmental protection applications.

  17. Fabrication of Fe3O4@CuO core-shell from MOF based materials and its antibacterial activity

    Science.gov (United States)

    Rajabi, S. K.; Sohrabnezhad, Sh.; Ghafourian, S.

    2016-12-01

    Magnetic Fe3O4@CuO nanocomposite with a core/shell structure was successfully synthesized via direct calcinations of magnetic Fe3O4@HKUST-1 in air atmosphere. The morphology, structure, magnetic and porous properties of the as-synthesized nano composites were characterized by using scanning electron microscope (SEM), transmission electron microscopy (TEM), powder X-ray diffraction (PXRD), and vibration sample magnetometer (VSM). The results showed that the nanocomposite material included a Fe3O4 core and a CuO shell. The Fe3O4@CuO core-shell can be separated easily from the medium by a small magnet. The antibacterial activity of Fe3O4-CuO core-shell was investigated against gram-positive and gram-negative bacteria. A new mechanism was proposed for inactivation of bacteria over the prepared sample. It was demonstrated that the core-shell exhibit recyclable antibacterial activity, acting as an ideal long-acting antibacterial agent.

  18. Synthesis of Fe3O4/C/TiO2 Magnetic Photocatalyst via Vapor Phase Hydrolysis

    Directory of Open Access Journals (Sweden)

    Fuzhi Shi

    2012-01-01

    Full Text Available A core/multi-shell-structured Fe3O4/C/TiO2 magnetic photocatalyst is prepared via vapor phase hydrolysis process. The as-synthesized core/multi-shell-structured composite is characterized by X-ray diffraction (XRD, field emission scanning electron microscopy (FE-SEM, transmission electron microscopy (TEM, high-resolution electron microscopy (HRTEM, N2 adsorption-desorption isotherm analyses, vibrating sample magnetometer (VSM, and ultraviolet-visible (UV-Vis absorption spectroscopy. TEM and HRTEM show that well-crystallized anatase TiO2 nanocrystals are immobilized on the surface of as-prepared Fe3O4/C microspheres with dimensions around 200 nm. N2 adsorption-desorption isotherm analysis shows that the obtained photocatalyst exists disorderedly mesoporous structure. The photocatalytic efficiency of the catalyst in degradation of methylene blue is evaluated, and the Fe3O4/C/TiO2 photocatalyst with low TiO2 content (37% has a relatively higher activity than commercial anatase TiO2. The intermediate carbon layer avoids the photodissolution of Fe3O4 effectively, and the recycling property is largely improved due to the existence of magnetic Fe3O4 core.

  19. La-EDTA coated Fe3O4 nanomaterial: preparation and application in removal of phosphate from water.

    Science.gov (United States)

    Yang, Jiao; Zeng, Qingru; Peng, Liang; Lei, Ming; Song, Huijuan; Tie, Boqing; Gu, Jidong

    2013-02-01

    La-EDTA-Fe3O4 was prepared by a chemical co-precipitation method. The magnetic composite was characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FT-IR). Furthermore, the adsorption properties of La-EDTA-Fe3O4 toward phosphate in water were investigated. The uptake rate of phosphate in water by La-EDTA-Fe3O4 was 3-1000 times than that of EDTA-Fe3O4, and reached 97.8% at 7 hr. The adsorption process agreed well with the Freundlich model and kinetics studies showed that the adsorption of phosphate proceeds according to pseudo second-order adsorption kinetics. The maximum removal rate was achieved at pH 6.0-7.0. The La-EDTA-Fe3O4 had good adsorption properties and could be separated well from aqueous solution by a permanent magnet. Therefore, this nanomaterial has potential application for the removal of phosphate from large water bodies.

  20. Production of nearly monodisperse Fe3O4 and Fe@Fe3O4 nanoparticles in aqueous medium and their surface modification for biomedical applications

    Science.gov (United States)

    Tegafaw, Tirusew; Xu, Wenlong; Lee, Sang Hyup; Chae, Kwon Seok; Chang, Yongmin; Lee, Gang Ho

    2017-02-01

    Iron (Fe)-based nanoparticles are extremely valuable in biomedical applications owing to their low toxicity and high magnetization values at room temperature. In this study, we synthesized nearly monodisperse iron oxide (Fe3O4) and Fe@Fe3O4 (core: Fe, shell: Fe3O4) nanoparticles in aqueous medium under argon flow and then, coated them with various biocompatible ligands and silica. In this study, eight types of surface-modified nanoparticles were investigated, namely, Fe3O4@PAA (PAA = polyacrylic acid; Mw of PAA = 5100 amu and 15,000 amu), Fe3O4@PAA-FA (FA = folic acid; Mw of PAA = 5100 amu and 15,000 amu), Fe3O4@PEI-fluorescein (PEI = polyethylenimine; Mw of PEI = 1300 amu), Fe@Fe3O4@PEI (Mw of PEI = 10,000 amu), Fe3O4@SiO2 and Fe@Fe3O4@SiO2 nanoparticles. We characterized the prepared surface-modified nanoparticles using high-resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), Fourier transform infrared (FT-IR) absorption spectroscopy, a superconducting quantum interference device (SQUID), X-ray photoelectron spectroscopy (XPS), photoluminescence (PL) spectroscopy and confocal microscopy. Finally, we measured the cytotoxicity of the samples. The results indicate that the surface-modified nanoparticles are biocompatible and are potential candidates for various biomedical applications.

  1. One-pot green synthesis of reduced graphene oxide (RGO)/Fe3O4 nanocomposites and its catalytic activity toward methylene blue dye degradation.

    Science.gov (United States)

    Vinothkannan, M; Karthikeyan, C; Gnana kumar, G; Kim, Ae Rhan; Yoo, Dong Jin

    2015-02-05

    The reduced graphene oxide (RGO)/Fe3O4 nanocomposites were synthesized through a facile one-pot green synthesis by using solanum trilobatum extract as a reducing agent. Spherical shaped Fe3O4 nanoparticles with the diameter of 18 nm were uniformly anchored over the RGO matrix and the existence of fcc structured Fe3O4 nanoparticles over the RGO matrix was ensured from X-ray diffraction patterns. The amide functional groups exist in the solanum trilobatum extract is directly responsible for the reduction of Fe(3+) ions and GO. The thermal stability of GO was increased by the removal of hydrophilic functional groups via solanum trilobatum extract and was further promoted by the ceramic Fe3O4 nanoparticles. The ID/IG ratio of RGO/Fe3O4 was increased over GO, indicating the extended number of structural defects and disorders in the RGO/Fe3O4 composite. The catalytic efficiency of prepared nanostructures toward methylene blue (MB) dye degradation mediated through the electron transfer process of BH4(-) ions was studied in detail. The π-π stacking, hydrogen bonding and electrostatic interaction exerted between the RGO/Fe3O4 composite and methylene blue, increased the adsorption efficiency of dye molecules and the large surface area and extended number of active sites completely degraded the MB dye within 12 min.

  2. One-pot green synthesis of reduced graphene oxide (RGO)/Fe3O4 nanocomposites and its catalytic activity toward methylene blue dye degradation

    Science.gov (United States)

    Vinothkannan, M.; Karthikeyan, C.; Gnana kumar, G.; Kim, Ae Rhan; Yoo, Dong Jin

    2015-02-01

    The reduced graphene oxide (RGO)/Fe3O4 nanocomposites were synthesized through a facile one-pot green synthesis by using solanum trilobatum extract as a reducing agent. Spherical shaped Fe3O4 nanoparticles with the diameter of 18 nm were uniformly anchored over the RGO matrix and the existence of fcc structured Fe3O4 nanoparticles over the RGO matrix was ensured from X-ray diffraction patterns. The amide functional groups exist in the solanum trilobatum extract is directly responsible for the reduction of Fe3+ ions and GO. The thermal stability of GO was increased by the removal of hydrophilic functional groups via solanum trilobatum extract and was further promoted by the ceramic Fe3O4 nanoparticles. The ID/IG ratio of RGO/Fe3O4 was increased over GO, indicating the extended number of structural defects and disorders in the RGO/Fe3O4 composite. The catalytic efficiency of prepared nanostructures toward methylene blue (MB) dye degradation mediated through the electron transfer process of BH4- ions was studied in detail. The π-π stacking, hydrogen bonding and electrostatic interaction exerted between the RGO/Fe3O4 composite and methylene blue, increased the adsorption efficiency of dye molecules and the large surface area and extended number of active sites completely degraded the MB dye within 12 min.

  3. Electrochemical sensing behaviour of Ni doped Fe3O4 nanoparticles

    Science.gov (United States)

    Suresh, R.; Giribabu, K.; Manigandan, R.; Vijayalakshmi, L.; Stephen, A.; Narayanan, V.

    2014-01-01

    Ni doped Fe3O4 nanoparticles were synthesized by simple hydrothermal method. The prepared nanomaterials were characterized by X-ray diffraction analysis, DRS-UV-Visible spectroscopy and field emission scanning electron microscopy. The XRD confirms the phase purity of the synthesized Ni doped Fe3O4 nanoparticles. The optical property of Ni doped Fe3O4 nanoparticles were studied by DRS UV-Visible analysis. The electrochemical sensing property of pure and Ni doped Fe3O4 nanoparticles were examined using uric acid as an analyte. The obtained results indicated that the Ni doped Fe3O4 nanoparticles exhibited higher electrocatalytic activity towards uric acid.

  4. Enhanced dechlorination of 2,4-dichlorophenol by recoverable Ni/Fe-Fe3O4 nanocomposites.

    Science.gov (United States)

    Xu, Cancan; Liu, Rui; Chen, Lvjun; Tang, Jialu

    2016-10-01

    Ni/Fe-Fe3O4 nanocomposites were synthesized for dechlorination of 2,4-dichlorophenol (2,4-DCP). The effects of the Ni content in Ni/Fe-Fe3O4 nanocomposites, solution pH, and common dissolved ions on the dechlorination efficiency were investigated, in addition to the reusability of the nanocomposites. The results showed that increasing content of Ni in Ni/Fe-Fe3O4 nanocomposites, from 1 to 5wt.%, greatly increased the dechlorination efficiency; the Ni/Fe-Fe3O4 nanocomposites had much higher dechlorination efficiency than bare Ni/Fe nanoparticles. Ni content of 5wt.% and initial pH below 6.0 was found to be the optimal conditions for the catalytic dechlorination of 2,4-DCP. Both 2,4-DCP and the intermediate product 2-chlorophenol (2-CP) were completely removed, and the concentration of the final product phenol was close to the theoretical phenol production from complete dechlorination of 20mg/L of 2,4-DCP, after 3hr reaction at initial pH value of 6.0, 3g/L Ni/Fe-Fe3O4, 5wt.% Ni content in the composite, and temperature of 22°C. 2,4-DCP dechlorination was enhanced by Cl(-) and inhibited by NO3(-) and SO4(2-). The nanocomposites were easily separated from the solution by an applied magnetic field. When the catalyst was reused, the removal efficiency of 2,4-DCP was almost 100% for the first seven uses, and gradually decreased to 75% in cycles 8-10. Therefore, the Ni/Fe-Fe3O4 nanocomposites can be considered as a potentially effective tool for remediation of pollution by 2,4-DCP.

  5. Rapid ultrasound-assisted magnetic microextraction of gallic acid from urine, plasma and water samples by HKUST-1-MOF-Fe3O4-GA-MIP-NPs: UV-vis detection and optimization study.

    Science.gov (United States)

    Asfaram, Arash; Ghaedi, Mehrorang; Dashtian, Kheibar

    2017-01-01

    Magnetite (Fe3O4 nanoparticles (NPs)) HKUST-1 metal organic framework (MOF) composite as a support was used for surface imprinting of gallic acid imprinted polymer (HKUST-1-MOF-Fe3O4-GA-MIP) using vinyltrimethoxysilane (VTMOS) as the cross-linker. Subsequently, HKUST-1-MOF-Fe3O4-NPs-GA-MIP characterized by FT-IR, XRD and FE-SEM analysis and applied for fast and selective and sensitive ultrasound assisted dispersive magnetic solid phase microextraction of gallic acid (GA) by UV-Vis (UA-DMSPME-UV-Vis) detection method. Plackett-Burman design (PBD) and central composite design (CCD) according to desirability function (DF) indicate the significant variables among the extraction factors vortex (mixing) time (min), sonication time (min), temperature (°C), eluent volume (L), pH and HKUST-1-MOF-Fe3O4-NPs-GA-MIP mass (mg) and their contribution on the response. Optimum conditions and values correspond to pH, HKUST-1-MOF-Fe3O4-NPs-GA-MIP mass, sonication time and the eluent volume were set as follow 3.0, 1.6mg, 4.0min and 180μL, respectively. The average recovery (ER%) of GA was 98.13% with desirability of 0.997, while the present method has best operational performance like wide linear range 8-6000ngmL(-1) with a Limit of detection (LOD) of 1.377ngmL(-1), limit of quantification (LOQ) 4.591ngmL(-1) and precision (recovery of GA in urine, human plasma and water samples within the range of 92.3-100.6% that strongly support high applicability of present method for real samples analysis, which candidate this method as promise for further application.

  6. Fe3O4@PFR纳米磁流体的制备及其表征%Preparation and characterization of Fe3O4@PFR magnetic nanofluid

    Institute of Scientific and Technical Information of China (English)

    李文烈; 马杰; 赵建涛

    2013-01-01

    以硫酸亚铁、苯酚和六次甲基四胺为原料,采用水热法制备出酚醛树脂(PFR)包覆的Fe3O4(Fe3O4@PFR)纳米粒子,分散于离子水中,得水基Fe3O4@PFR磁性纳米流体,经过X-射线衍射仪(XRD)、傅里叶红外光谱仪(FTIR)、扫描电子显微镜(SEM)、透射电子显微镜(TEM)和振动磁强计(VSM)进行表征.结果表明,Fe3O4纳米晶体的平均粒径为20 nm,在室温下表现为超顺磁性,Fe3O4@PFR磁性纳米流体具有很好的稳定性和生物相容性.%Ferrous sulfate,phenol and hexamethylene tetramine as raw materials. Using hydrothermal syn-thesis of phenolic resin coated Fe3O4(Fe3O4@ PFR) nanoparticles,dispersing in deionized water,Fe3O4 @ PFR magentic nanofluid was obtained. The products are characterized by XRD, FTIR, SEM, TEM and VSM instruments. The results showed that Fe3 O4 nanocrystals around 20 nm size possess excellent super-paramagnetic properties at room temperature. Fe3O4@ PFR magnetic nanofluids possess outstanding stabil-ity with good biological compatibility.

  7. One-step synthesis of novel PANI-Fe3O4@ZnO core-shell microspheres: An efficient photocatalyst under visible light irradiation

    Science.gov (United States)

    Zhang, Xiaoyuan; Wu, Jianning; Meng, Guihua; Guo, Xuhong; Liu, Chang; Liu, Zhiyong

    2016-03-01

    For the first time, novel multifunctional superparamagnetic PANI-Fe3O4@ZnO core-shell composite photocatalysts with different PANI: ZnO ratios were synthesized by Pickering emulsion route in one step in the presence of ZnO nanoparticles. PANI-Fe3O4@ZnO core-shell microspheres consist of PANI core which embedded with Fe3O4-OA (oleic acid modified Fe3O4) nanoparticles and tunable ZnO shell thickness. The resulting samples were thoroughly studied by using X-ray diffraction (XRD), X-ray photoelectron spectra (XPS), transmission electron microscopy (TEM), scanning electron microscope (SEM) and energy dispersive X-ray spectroscopy (EDS). The catalytic activity of the as-prepared PANI-Fe3O4@ZnO core-shell microspheres is investigated by the degradation of MB under visible light irradiation. As expected, the as prepared PANI-Fe3O4@ZnO photocatalysts exhibit highly enhanced photocatalytic activities in the degradation of MB under visible light irradiation owing to fast separation of photo-generated electron-hole pairs. Significantly, the PANI-Fe3O4@ZnO catalysts can be separated from the reaction media by applying an external magnet, and can be reused for seven cycles without change in stability and degradation efficiency.

  8. Rapid degradation of methylene blue in a novel heterogeneous Fe3O4 @rGO@TiO2-catalyzed photo-Fenton system.

    Science.gov (United States)

    Yang, Xiaoling; Chen, Wei; Huang, Jianfei; Zhou, Ying; Zhu, Yihua; Li, Chunzhong

    2015-05-22

    Herein, a ternary nanocomposite with TiO2 nanoparticles anchored on reduced graphene oxide (rGO)-encapsulated Fe3O4 spheres (Fe3O4@rGO@TiO2) is presented as a high efficient heterogeneous catalyst for photo-Fenton degradation of recalcitrant pollutants under neutral pH. Fe3O4@rGO@TiO2 was synthesized by depositing TiO2 nanoparticles on the surface of the Fe3O4 spheres wrapped by graphene oxide (GO) which was obtained by an electrostatic layer-by-layer method. This as-prepared catalyst reflected good ferromagnetism and superior stability which makes it convenient to be separated and recycled. Due to the synergic effects between the different components composed the catalyst, swift reduction of Fe(3+) can be achieved to regenerate Fe(2+). Fe3O4@rGO@TiO2 exhibited enhancing catalytic activity for the degradation of azo-dyes compared with Fe3O4, Fe3O4@SiO2@TiO2 or SiO2@rGO@TiO2, further conforming the rapid redox reaction between Fe(2+) and Fe(3+). All these merits indicate that the composite catalyst possesses great potential for visible-light driven destruction of organic compounds.

  9. Rapid degradation of methylene blue in a novel heterogeneous Fe3O4 @rGO@TiO2-catalyzed photo-Fenton system

    Science.gov (United States)

    Yang, Xiaoling; Chen, Wei; Huang, Jianfei; Zhou, Ying; Zhu, Yihua; Li, Chunzhong

    2015-05-01

    Herein, a ternary nanocomposite with TiO2 nanoparticles anchored on reduced graphene oxide (rGO)-encapsulated Fe3O4 spheres (Fe3O4@rGO@TiO2) is presented as a high efficient heterogeneous catalyst for photo-Fenton degradation of recalcitrant pollutants under neutral pH. Fe3O4@rGO@TiO2 was synthesized by depositing TiO2 nanoparticles on the surface of the Fe3O4 spheres wrapped by graphene oxide (GO) which was obtained by an electrostatic layer-by-layer method. This as-prepared catalyst reflected good ferromagnetism and superior stability which makes it convenient to be separated and recycled. Due to the synergic effects between the different components composed the catalyst, swift reduction of Fe3+ can be achieved to regenerate Fe2+. Fe3O4@rGO@TiO2 exhibited enhancing catalytic activity for the degradation of azo-dyes compared with Fe3O4, Fe3O4@SiO2@TiO2 or SiO2@rGO@TiO2, further conforming the rapid redox reaction between Fe2+ and Fe3+. All these merits indicate that the composite catalyst possesses great potential for visible-light driven destruction of organic compounds.

  10. Recent advances in the synthesis of Fe3O4@AU core/shell nanoparticles

    Science.gov (United States)

    Salihov, Sergei V.; Ivanenkov, Yan A.; Krechetov, Sergei P.; Veselov, Mark S.; Sviridenkova, Natalia V.; Savchenko, Alexander G.; Klyachko, Natalya L.; Golovin, Yury I.; Chufarova, Nina V.; Beloglazkina, Elena K.; Majouga, Alexander G.

    2015-11-01

    Fe3O4@Au core/shell nanoparticles have unique magnetic and optical properties. These nanoparticles are used for biomedical applications, such as magnetic resonance imaging, photothermal therapy, controlled drug delivery, protein separation, biosensors, DNA detection, and immunosensors. In this review, recent methods for the synthesis of core/shell nanoparticles are discussed. We divided all of the synthetic methods in two groups: methods of synthesis of bi-layer structures and methods of synthesis of multilayer composite structures. The latter methods have a layer of "glue" material between the core and the shell.

  11. Encapsulation of Fe3O4 Nanoparticles into N, S co-Doped Graphene Sheets with Greatly Enhanced Electrochemical Performance

    Science.gov (United States)

    Yang, Zunxian; Qian, Kun; Lv, Jun; Yan, Wenhuan; Liu, Jiahui; Ai, Jingwei; Zhang, Yuxiang; Guo, Tailiang; Zhou, Xiongtu; Xu, Sheng; Guo, Zaiping

    2016-01-01

    Particular N, S co-doped graphene/Fe3O4 hybrids have been successfully synthesized by the combination of a simple hydrothermal process and a subsequent carbonization heat treatment. The nanostructures exhibit a unique composite architecture, with uniformly dispersed Fe3O4 nanoparticles and N, S co-doped graphene encapsulant. The particular porous characteristics with many meso/micro holes/pores, the highly conductive N, S co-doped graphene, as well as the encapsulating N, S co-doped graphene with the high-level nitrogen and sulfur doping, lead to excellent electrochemical performance of the electrode. The N-S-G/Fe3O4 composite electrode exhibits a high initial reversible capacity of 1362.2 mAhg−1, a high reversible specific capacity of 1055.20 mAhg−1 after 100 cycles, and excellent cycling stability and rate capability, with specific capacity of 556.69 mAhg−1 when cycled at the current density of 1000 mAg−1, indicating that the N-S-G/Fe3O4 composite is a promising anode candidate for Li-ion batteries. PMID:27296103

  12. Encapsulation of Fe3O4 Nanoparticles into N, S co-Doped Graphene Sheets with Greatly Enhanced Electrochemical Performance

    Science.gov (United States)

    Yang, Zunxian; Qian, Kun; Lv, Jun; Yan, Wenhuan; Liu, Jiahui; Ai, Jingwei; Zhang, Yuxiang; Guo, Tailiang; Zhou, Xiongtu; Xu, Sheng; Guo, Zaiping

    2016-06-01

    Particular N, S co-doped graphene/Fe3O4 hybrids have been successfully synthesized by the combination of a simple hydrothermal process and a subsequent carbonization heat treatment. The nanostructures exhibit a unique composite architecture, with uniformly dispersed Fe3O4 nanoparticles and N, S co-doped graphene encapsulant. The particular porous characteristics with many meso/micro holes/pores, the highly conductive N, S co-doped graphene, as well as the encapsulating N, S co-doped graphene with the high-level nitrogen and sulfur doping, lead to excellent electrochemical performance of the electrode. The N-S-G/Fe3O4 composite electrode exhibits a high initial reversible capacity of 1362.2 mAhg‑1, a high reversible specific capacity of 1055.20 mAhg‑1 after 100 cycles, and excellent cycling stability and rate capability, with specific capacity of 556.69 mAhg‑1 when cycled at the current density of 1000 mAg‑1, indicating that the N-S-G/Fe3O4 composite is a promising anode candidate for Li-ion batteries.

  13. Preparation of multi-functionalized Fe3O4/Au nanoparticles for medical purposes.

    Science.gov (United States)

    del Mar Ramos-Tejada, María; Viota, Julian L; Rudzka, Katarzyna; Delgado, Angel V

    2015-04-01

    In this work, we investigate a route towards the synthesis of multi-functionalized nanoparticles for medical purposes. The aim is to produce magnetite/gold (Fe3O4/Au) nanoparticles combining several complementary properties, specifically, being able to carry simultaneously an antitumor drug and a selected antibody chosen so as to improve specificity of the drug vehicle. The procedure included, firstly, the preparation of Fe3O4 cores coated with Au nanoparticles: this was achieved by using initially the layer-by-layer technique in order to coat the magnetite particles with a three polyelectrolyte (cationic-anionic-cationic) layer. With this, the particles became a good substrate for the growth of the gold layer in a well-defined core-shell structure. The resulting nanoparticles benefit from the magnetic properties of the magnetite and the robust chemistry and the biostability of gold surfaces. Subsequently, the Fe3O4/Au nanoparticles were functionalized with a humanized monoclonal antibody, bevacizumab, and a chemotherapy drug, doxorubicin. Taken together, bevacizumab enhances the therapeutic effect of chemotherapy agents on some kinds of tumors. In this work we first discuss the morphology of the particles and the electrical characteristics of their surface in the successive synthesis stages. Special attention is paid to the chemical stability of the final coating, and the physical stability of the suspensions of the nanoparticles in aqueous solutions and phosphate buffer. We describe how optical absorbance and electrokinetic data provide a follow up of the progress of the nanostructure formation. Additionally, the same techniques are employed to demonstrate that the composite nanoparticles are capable of loading/releasing doxorubicin and/or bevacizumab.

  14. Fluorescent magnetic Fe3 O4 /rare Earth colloidal nanoparticles for dual-modality imaging.

    Science.gov (United States)

    Zhu, Haie; Shang, Yalei; Wang, Wenhao; Zhou, Yingjie; Li, Penghui; Yan, Kai; Wu, Shuilin; Yeung, Kelvin W K; Xu, Zushun; Xu, Haibo; Chu, Paul K

    2013-09-09

    Fluorescent magnetic colloidal nanoparticles (FMCNPs) are produced by a two-step, seed emulsifier-free emulsion polymerization in the presence of oleic acid and sodium undecylenate-modified Fe3 O4 nanoparticles (NPs). The Fe3 O4 /poly(St-co-GMA) nanoparticles are first synthesized as the seed and Eu(AA)3 Phen is copolymerized with the remaining St and GMA to form the fluorescent polymer shell in the second step. The uniform core-shell structured FMCNPs with a mean diameter of 120 nm exhibit superparamagnetism with saturation magnetization of 1.92 emu/g. Red luminescence from the FMCNPs is confirmed by the salient fluorescence emission peaks of europium ions at 594 and 619 nm as well as 2-photon confocal scanning laser microscopy. The in vitro cytotoxicity test conducted using the MTT assay shows good cytocompatibility and the T2 relaxivity of the FMCNPs is 353.86 mM(-1) S(-1) suggesting its potential in magnetic resonance imaging (MRI). In vivo MRI studies based on a rat model show significantly enhanced T2 -weighted images of the liver after administration and prussian blue staining of the liver tissue slice reveals accumulation of FMCNPs in the organ. The cytocompatibility, superparamagnetism, and excellent fluorescent properties of FMCNPs make them suitable for biological imaging probes in MRI and optical imaging.

  15. Magnetically Separable Fe3O4/AgBr Hybrid Materials: Highly Efficient Photocatalytic Activity and Good Stability

    Science.gov (United States)

    Cao, Yuhui; Li, Chen; Li, Junli; Li, Qiuye; Yang, Jianjun

    2015-06-01

    Magnetically separable Fe3O4/AgBr hybrid materials with highly efficient photocatalytic activity were prepared by the precipitation method. All of them exhibited much higher photocatalytic activity than the pure AgBr in photodegradation of methyl orange (MO) under visible light irradiation. When the loading amount of Fe3O4 was 0.5 %, the hybrid materials displayed the highest photocatalytic activity, and the degradation yield of MO reached 85 % within 12 min. Silver halide often suffers serious photo-corrosion, while the stability of the Fe3O4/AgBr hybrid materials improved apparently than the pure AgBr. Furthermore, depositing Fe3O4 onto the surface of AgBr could facilitate the electron transfer and thereby leading to the elevated photocatalytic activity. The morphology, phase structure, and optical properties of the composites were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), UV-visible diffuse reflectance spectra (UV-vis DRS), and photoluminescence (PL) techniques.

  16. Synthesis and microwave absorption properties of graphene-oxide(GO)/polyaniline nanocomposite with Fe3O4 particles

    Institute of Scientific and Technical Information of China (English)

    耿欣; 何大伟; 王永生; 赵文; 周亦康; 李树磊

    2015-01-01

    In order to investigate the impedance matching properties of microwave absorbers, the ternary nanocomposites of GO/PANI/Fe3O4 (GPF) are prepared via a two-step method, GO/PANI composites are synthesized by dilute polymerization in the presence of aniline monomer and GO, and GO/PANI/Fe3O4 is prepared via a co-precipitation method. The obtained nanocomposites are characterized by scanning electron microscope (SEM), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FTIR), respectively. The microwave absorbability reveals enhanced microwave absorption properties compared with GO, PANI, and GO/PANI. The maximum reflection loss of GO/PANI/Fe3O4 is up to−27 dB at 14 GHz with its thickness being 2 mm, and its absorption bandwidths exceeding−10 dB are more than 11.2 GHz with its thickness values being in a range of 1.5 mm–4 mm. It provides that GO/PANI/Fe3O4 can be used as an attractive candidate for microwave absorbers.

  17. Synthesis of flexible Fe3O4/C nanofibers with buffering volume expansion performance and their application in lithium-ion batteries

    Science.gov (United States)

    Wu, Qianhui; Zhao, Rongfang; Zhang, Xiue; Li, Wenlong; Xu, Renhua; Diao, Guowang; Chen, Ming

    2017-08-01

    Freestanding binder-free electrodes, as a new generation of electrode material, can effectively improve the energy density of lithium-ion batteries (LIBs). In this paper, novel structured Fe3O4/C composite nanofibers are successful synthesized by a simple electrospinning method followed by a thermal treatment process. The composite nanofibers have the unique internal voids between Fe3O4 nanoparticles and carbon matrix. The Fe3O4/C nanofibers film with good flexibility and excellent electrical conductivity can be directly used to fabricate half-cell without any current collector, binder and additional conductive agent. As anode material for LIBs, the Fe3O4/C composite nanofibers deliver high reversible capacity (762 mA h g-1 at 0.5 A g-1 after 300 cycles). The results show that the internal voids in flexible Fe3O4/C composite nanofibers effectively buffer volume expansion of Fe3O4 in lithium ion intercalation/deintercalation process and avoid the fracture of the nanofibers, which retain the structural integrity and improve the cycling stability of electrode. Therefore, the design and synthesis strategy of flexible nanofibers film are prospective for applications in next-generation flexible LIBs.

  18. Fast synthesis of dopamine-coated Fe3O4 nanoparticles through ligand-exchange method

    Institute of Scientific and Technical Information of China (English)

    Peng An; Fang Zuo; Yuan Peng Wu; Jun Hua Zhang; Zhao Hui Zheng; Xiao Bin Ding; Yu Xing Peng

    2012-01-01

    A fast approach was described for the synthesis of water-dispersible monodisperse dopamine-coated Fe3O4 nanoparticles (DA-Fe3O4) with uniform size and shape via ligand-exchange of oleic acid on Fe3O4 using only 2 min.The prepared DA-Fe3O4 nanoparticles were characterized by transmission electron microscopy,Fourier transform infrared spectrometry,and vibrating sample magnetometer.The results indicated that the resulting DA-Fe3O4 nanoparticles had an average diameter of about 19.2 nm.The magnetic saturation value of the prepared DA-Fe3O4 nanoparticles was determined to be 72.87 emu/g,which indicating a wellestablished superparamagnetic property.

  19. A moderate method for preparation DMSA coated Fe3O4 nanoparticles

    Science.gov (United States)

    Song, L. N.; Gu, N.; Zhang, Y.

    2017-01-01

    A moderate way to prepare water soluble magnetic Fe3O4 nanoparticles has been developed. Firstly, oleic acid coated Fe3O4 is prepared by coprecipitation. Second, oleic acid were replaced by 2,3-dimercaptosuccinnic acid (DMSA) to prepare DMSA/Fe3O4 in the mixed solution of n-hexane and acetone. After dialysis and filtration the DMSA/Fe3O4 can be transferred into distilled water to form stable Fe3O4 nanoparticle solutions. The TEM images indicated that the particles had spherical shape and the nanoparticles were found to be 12 nm with a relatively narrow size distribution with the hydrodynamic size of 30 nm. And the result of VSM shows that DMSA/Fe3O4 nanoparticles have a saturation magnetization of 31 emu/g. The IR spectra indicated that the iron oxide was located by carboxyl matrix.

  20. Sol-gel derived silica/chitosan/Fe3O4 nanocomposite for direct electrochemistry and hydrogen peroxide biosensing

    Science.gov (United States)

    Satvekar, R. K.; Rohiwal, S. S.; Tiwari, A. P.; Raut, A. V.; Tiwale, B. M.; Pawar, S. H.

    2015-01-01

    A novel strategy to fabricate hydrogen peroxide third generation biosensor has been developed from sol-gel of silica/chitosan (SC) organic-inorganic hybrid material assimilated with iron oxide magnetic nanoparticles (Fe3O4). The large surface area of Fe3O4 and porous morphology of the SC composite facilitates a high loading of horseradish peroxidase (HRP). Moreover, the entrapped enzyme preserves its conformation and biofunctionality. The fabrication of hydrogen peroxide biosensor has been carried out by drop casting of the SC/F/HRP nanocomposite on glassy carbon electrode (GCE) for study of direct electrochemistry. The x-ray diffraction (XRD) pattern and transmission electron microscopy (TEM) confirms the phase purity and particle size of as-synthesized Fe3O4 nanoparticles, respectively. The nanocomposite was characterized by UV-vis spectroscopy, fluorescence spectroscopy and Fourier transform infrared (FTIR) for the characteristic structure and conformation of enzyme. The surface topographies of the nanocomposite thin films were investigated by scanning electron microscopy (SEM). Dynamic light scattering (DLS) was used to determine the particle size distribution. The electrostatic interactions of the SC composite with Fe3O4 nanoparticles were studied by the zeta potential measurement. Electrochemical impedance spectroscopy (EIS) of the SC/F/HRP/GCE electrode displays Fe3O4 nanoparticles as an excellent candidate for electron transfer. The SC/F/HRP/GCE exhibited a pair of well-defined quasi reversible cyclic voltammetry peaks due to the redox couple of HRP-heme Fe (III)/Fe (II) in pH 7.0 potassium phosphate buffer. The biosensor was employed to detect H2O2 with linear range of 5 μM to 40 μM and detection limit of 5 μM. The sensor displays excellent selectivity, sensitivity, good reproducibility and long term stability.

  1. Synthesis and Identification of Fe3o4/Clinoptilolite Magnetic Nanocomposite

    OpenAIRE

    A. mollahosseini; M. Toghroli

    2015-01-01

    In the present work, magnetic zeolitehave been synthesized by insitu method using combination of iron oxide nanoparticlesFe3O4 and clinoptilolite. Fe3O4nanoparticleshave been synthesized electrochemically and then clinoptilolitewas added to solution. The Fe3O4 nanoparticles synthesized at the temperature of 90? C with applying the potential of 8V for 1800 seconds. The synthesized nanocomposite characterized by IR spectra,scanning electron microscopy (SEM) and XRD methods.Results shows that na...

  2. Electrochemical sensing property of Mn doped Fe3O4 nanoparticles

    Science.gov (United States)

    Suresh, R.; Giribabu, K.; Manigandan, R.; Vijayalakshmi, L.; Stephen, A.; Narayanan, V.

    2013-02-01

    The Mn doped Fe3O4 nanoparticles were synthesized by hydrothermal method. The prepared nanoparticles were characterized by X-ray diffraction (XRD) analysis, UV-Visible spectroscopy (UV-Vis) and field emission scanning electron microscopy (FE-SEM). The electrochemical sensing property of pure and Mn doped Fe3O4 nanoparticles were examined using uric acid (UA) as an analyte. The obtained results indicated that the Mn doped Fe3O4 nanoparticles exhibited higher electrocatalytic activity towards UA.

  3. Influence of nanographene platelets (NGP) incorporation on Fe3O4 nanoparticles as materials additives for enhancement thermal properties stearic acid

    Science.gov (United States)

    Nuryadin, M. K.; Andiarto, R.; Taufik, A.; Saleh, R.

    2016-11-01

    In this work, Fe3O4 nanoparticles, and Fe3O4/NGP composite were used as material additive for enhancement thermal properties of stearic acid (SA). The both material additive were synthesized using sol-gel method. Phase change material (PCM) composites SA-Fe3O4 and Sa-Fe3O4/NGP mixtures were made through the dispersion technique with three different weight % ratio of material additives into stearic acid: 1 wt.%, 3 wt.%, and 5 wt.%. X-Ray Diffractometer (XRD) and Fourier Transform Infrared (FTIR) spectroscopy were used to investigate the structural properties. Magnetic properties also measured by vibrating sample magnetometer (VSM) to see influence of NGP in PCM composites. Differential Scanning Calorimetry (DSC) and Thermogravimetric Analysis (TGA) were used in order to analyse the thermal properties of the samples. The results show an enhancement of the latent heat, thermal stability as well as specific heat by the presence of material additives in SA. Compare to SA- Fe3O4, SA-Fe3O4/NGP show better improvement in enhancement of thermal performance of SA. The improvement by about 41.2% in specific heat and 21.2% in latent heat.

  4. One-Pot Synthesis of Pomegranate-Structured Fe3 O4 /Carbon Nanospheres-Doped Graphene Aerogel for High-Rate Lithium Ion Batteries.

    Science.gov (United States)

    He, Dafang; Li, Lixian; Bai, Fengjuan; Zha, Chenyang; Shen, Liming; Kung, Harold H; Bao, Ningzhong

    2016-03-18

    A unique hierarchically nanostructured composite of iron oxide/carbon (Fe3O4/C) nanospheres-doped three-dimensional (3D) graphene aerogel has been fabricated by a one-pot hydrothermal strategy. In this novel nanostructured composite aerogel, uniform Fe3O4 nanocrystals (5-10 nm) are individually embedded in carbon nanospheres (ca. 50 nm) forming a pomegranate-like structure. The carbon matrix suppresses the aggregation of Fe3O4 nanocrystals, avoids direct exposure of the encapsulated Fe3O4 to the electrolyte, and buffers the volume expansion. Meanwhile, the interconnected 3D graphene aerogel further serves to reinforce the structure of the Fe3O4/C nanospheres and enhances the electrical conductivity of the overall electrode. Therefore, the carbon matrix and the interconnected graphene network entrap the Fe3O4 nanocrystals such that their electrochemical function is retained even after fracture. This novel hierarchical aerogel structure delivers a long-term stability of 634 mA h g(-1) over 1000 cycles at a high current density of 6 A g(-1) (7 C), and an excellent rate capability of 413 mA h g(-1) at 10 A g(-1) (11 C), thus exhibiting great potential as an anode composite structure for durable high-rate lithium-ion batteries.

  5. Synthesis, characterization and magnetorheological study of 3-aminopropyltriethoxysilane-modified Fe3O4 nanoparticles

    Science.gov (United States)

    Wang, Guangshuo; Ma, Yingying; Tong, Yu; Dong, Xufeng

    2016-03-01

    In this study, monodisperse Fe3O4 nanoparticles were synthesized successfully using a sonochemical method in the presence of 3-aminopropyltriethoxysilane (APTES). The morphology, microstructure and magnetic properties of the bare Fe3O4 and APTES-coated Fe3O4 were investigated in detail by TEM, XRD, FTIR and SQUID. It was found that APTES-coated Fe3O4 showed relatively good dispersion with a narrow size distribution of 8.4 ± 2.1 nm diameter. The functionalization of Fe3O4 was proved to be covalent linking between Fe3O4 and APTES. The field-dependent magnetization curve indicated superparamagnetic behavior of Fe3O4-APTES with a saturation magnetization (M s) of 70.5 emu g-1 at room temperature. A magnetorheological (MR) fluid was prepared using the obtained Fe3O4-APTES nanoparticles with 25 wt% particles, and its MR properties were tested using a Physica MCR301 rheometer fitted with an MRmodule. The results showed that the as-prepared APTES-coated Fe3O4 nanoparticle-based MR fluid exhibited typical MR effects, with increasing viscosity, shear stress and yield stress depending on the applied magnetic field strength.

  6. Surface organic modification of Fe3O4 nanoparticles by silane-coupling agents

    Institute of Scientific and Technical Information of China (English)

    CUI Sheng; SHEN Xiaodong; LIN Benlan

    2006-01-01

    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 .

  7. Ferroferric oxide/polystyrene (Fe3O4/PS superparamagnetic nanocomposite via facile in situ bulk radical polymerization

    Directory of Open Access Journals (Sweden)

    2010-03-01

    Full Text Available Organo-modified ferroferric oxide superparamagnetic nanoparticles, synthesized by the coprecipitation of superparamagnetic nanoparticles in presence of oleic acid (OA, were incorporated in polystyrene (PS by the facile in situ bulk radical polymerization by using 2,2-azobisisobutyronitrile (AIBN as initiator. The transmission electron microscopy (TEM analysis of the resultant uniform ferroferric oxide/polystyrene superparamagnetic nanocomposite (Fe3O4/PS showed that the superparamagnetic nanoparticles had been dispersed homogeneously in the polymer matrix due to the surface grafted polystyrene, confirmed by Fourier transform infrared (FT-IR spectroscopy and thermogravimetric analysis (TGA. The superparamagnetic property of the Fe3O4/PS nanocomposite was testified by the vibrating sample magnetometer (VSM analysis. The strategy developed is expected to be applied for the large-scale industrial manufacturing of the superparamagnetic polymer nanocomposite.

  8. Synthesis and Characterization of Magnetized Photocatalyst Fe3O4/SiO2/TiO2 by Heteroagglomeration Method

    Science.gov (United States)

    Hasnah Dewi, Sari; Sutanto; Fisli, A.; Wardiyati, S.

    2016-08-01

    Magnetic photocatalysts Fe3O4/SiO2/TiO2 have been prepared using heteroagglomeration method. Synthesis of magnetic photocatalyst Fe3O4/SiO2/TiO2 was carried out through four stages : (1) synthesis of photocatalyst TiO2 nanoparticles by TiCl4 coprecipitation in ammonia solution, (2) synthesis of Fe3O4 nanoparticles through precipitation method using a mixture of Fe (III) / Fe (II) (2: 1 mole ratio) in ammonia solution, (3) coating with SiO2 through hydrolysis of silicate ion, (4) in the final stage, Fe3O4/SiO2 was mixed with TiO2 in hetero-agglomeration manner. Structure and morphology of resultan composites have been investigated by X-ray diffraction (XRD), Vibrating sample magnetometer (VSM), Fourier transform infrared (FTIR) and Transmission electron microscopy (TEM) were confirmed that composite Fe3O4/SiO2/TiO2 succefully synthesized. The functionality photocatalyst of the particles was tested by eliminating of methylene blue (MB) under UV light. The result showed the magnetite photocatalyst Fe3O4/SiO2/TiO2 has phototacalytic and absorbtion properties so that it has good performance at dyes removal in water higher than pure TiO2, and capable to perform repeatition process at least 4 times.

  9. 磁性纳米粒子Fe3O4@Au和Fe3O4@Ag的制备及表征%Synthesis and Characterization of Magnetic Fe3O4@Au and Fe3O4 @Ag Nanoparticles

    Institute of Scientific and Technical Information of China (English)

    庄严; 周群; 周全法

    2011-01-01

    利用化学共沉淀法将铁盐和亚铁盐溶液按一定比例混合制备磁性纳米Fe3O4,再用3-巯基丙基三甲氧基硅烷修饰磁性粒子,连接金、银纳米粒子制备了核壳结构的功能性微粒.通过X-射线粉末衍射(XRD)、透射电子显微镜(TEM)及紫外-可见光吸收光谱仪(UV - Vis)对粒子的结构与性质进行表征.结果表明:磁性Fe3O4纳米粒子属立方晶型,Fe3O4@Au和Fe3O4@Ag粒子包裹完全,形状趋近于球形,兼有磁性和金、银纳米粒子的特性,对硝基化合物具有良好的催化性能.%Magnetic nanoparticles of Fe3O4 were prepared by co - deposition. Fe3O4 and gold/silver nano-particles were conjoined with (3 - mercapto - propyl) trimethoxysilane, and then core - shell functional Fe3O4@ Au and Fe3O4@ Ag nanoparticles were prepared by multi - step reduction with sodiumcitrate. These particles were characterized by TEM, XRD, UV - Vis. The analysis results showed that the prepared Fe3O4 nanoparticles are cubic structure. Spherical Fe3O4@ Au and Fe3O4@ Ag nanoparticles have excellent catalytic activity for the reduction of nitrocompounds by borohydride.

  10. Preparation of CNC-dispersed Fe3O4 nanoparticles and their application in conductive paper.

    Science.gov (United States)

    Liu, Kai; Nasrallah, Joseph; Chen, Lihui; Huang, Liulian; Ni, Yonghao

    2015-08-01

    Well-dispersed Fe3O4 nanoparticles (NPs) were synthesized by a co-precipitation method in the presence of cellulose nano-crystals (CNC) as the template. The thus prepared Fe3O4 NPs were then used as a coating agent for the preparation of conductive paper. Fourier transform infrared spectroscopy (FTIR) results revealed that the Fe3O4 NPs were immobilized on the CNC through interactions between the hydroxyl groups of CNC and Fe3O4. Scanning transmission electron microscopy (STEM) images showed that the Fe3O4 NPs prepared in the presence of CNC can be dispersed in the CNC network, while the Fe3O4 NPs prepared in the absence of CNC tended to aggregate in aqueous solutions. The conductivity of the Fe3O4 NPs coated paper can reach to 0.0269 S/m at the coating amount of 14.75 g/m(2) Fe3O4/CNC nanocomposites. Therefore, the thus obtained coated paper can be potentially used as anti-static packaging material in the packaging field.

  11. Effect of MgO on Oxidation Process of Fe3 O4 in Pellets

    Institute of Scientific and Technical Information of China (English)

    Qiang-jian GAO; Yan-song SHEN; Xin JIANG; Hai-yan ZHENG; Feng-man SHEN; Chang-sheng LIU

    2016-01-01

    Induration process of oxidized pellets involves the oxidation of Fe3 O4 and re-crystallization of Fe2 O3 .The oxidation process of Fe3 O4 is significant for pellets to obtain better ambient strength.Thus,the effect of MgO on oxidation process of Fe3 O4 was investigated.The unreacted core model was applied to analyze the oxidizing indura-tion process of pellets.The experimental results show that MgO plays a negative role in the oxidation process of Fe3 O4 .The oxidation rate of Fe3 O4 in MgO-fluxed pellets (95.0% Fe3 O4+5.0% MgO)is slower than that in standard acid pellets (100% Fe3 O4 ).The relation between oxidation ratio of Fe3 O4 and time was calculated based on the unreacted core model for both MgO-fluxed pellets and standard acid pellets.According to verification experi-ments,the values calculated by model coincide well with the experimental values.Therefore,the unreacted core model could be applied to describe the oxidizing induration process of pellets.

  12. Biomimetic Mussel Adhesive Inspired Clickable Anchors Applied to the Functionalization of Fe3O4 Nanoparticles

    NARCIS (Netherlands)

    Goldmann, Anja S.; Schoedel, Christine; Walther, Andreas; Yuan, Jiayin; Loos, Katja; Mueller, Axel H. E.; Müller, Axel H.E.

    2010-01-01

    The functionalization of magnetite (Fe3O4) nanoparticles with dopamine-derived clickable biomimetic anchors is reported. Herein, an alkyne-modified catechol-derivative is employed as the anchor, as i) the catechol-functional anchor groups possess irreversible covalent binding affinity to Fe3O4 nanop

  13. Biomimetic Mussel Adhesive Inspired Clickable Anchors Applied to the Functionalization of Fe3O4 Nanoparticles

    NARCIS (Netherlands)

    Goldmann, Anja S.; Schoedel, Christine; Walther, Andreas; Yuan, Jiayin; Loos, Katja; Mueller, Axel H. E.; Müller, Axel H.E.

    2010-01-01

    The functionalization of magnetite (Fe3O4) nanoparticles with dopamine-derived clickable biomimetic anchors is reported. Herein, an alkyne-modified catechol-derivative is employed as the anchor, as i) the catechol-functional anchor groups possess irreversible covalent binding affinity to Fe3O4 nanop

  14. Spectroscopic characterization of magnetic Fe3O4@Au core shell nanoparticles

    Science.gov (United States)

    Fouad, Dina M.; El-Said, Waleed A.; Mohamed, Mona B.

    2015-04-01

    The magnetic nanoparticles iron oxide (Fe3O4) nanoparticles and iron oxide/gold core-shell (Fe3O4/Au) nanoparticles were synthesized and their catalytic photo-degradation activity towards malathion as example of organophosphorus pesticides were reported. Iron oxide (Fe3O4) magnetic nanoparticle was successfully prepared through co-precipitation method by the reduction of ferric chloride (FeCl3) using ascorbic acid. The morphology of the prepared nanoparticles was characterized by the TEM and XRD (X-ray diffraction) techniques. Degradation of 10 ppm of malathion in the presence of these nanoparticles under UV radiation was monitored using (HPLC) and UV-visible spectra. Fe3O4/Au nanoparticles showed higher efficiency in photo-degradation of malathion than Fe3O4 ones.

  15. Physical Chemistry Properties of Fe3O4 @ Cyclodextrin@ (12, 12 Swcnts as a Catalyst

    Directory of Open Access Journals (Sweden)

    Zeynab Abbasi

    2017-02-01

    Full Text Available Fe3O4 is used in the water gas shift reaction as a catalyst in the “Haber process”. In this work, the physical and chemical properties of Fe3O4 @ -Cyclodextrin @ (12, 12 SWCNTs has been investigated. Our calculations have been done in point of chemical phenomenon and electronic properties. The Magnetic behavior , Electron densities and electrical properties such as NMR Shielding, potential energies densities, energy density , ellipticity for electron densities , ELF, LOL, index of eta and finally ECP for Fe3O4 @ -Cyclodextrin@ (12, 12 SWCNTs have been calculated and simulated in our system. Our Calculation indicate that the Fe3O4 @ -Cyclodextrin@ (12, 12 SWCNTs are suitable surfaces for Fe3O4 such silica surfaces.

  16. 溶剂热法制备纳米Fe3O4粉体%Solvothermal Synthesis of Fe3O4 Nanopowders

    Institute of Scientific and Technical Information of China (English)

    刘冰; 李晓忆; 刘文宝; 姜付义

    2013-01-01

    Fe3 O4 nanoparticles are synthesized by the thermal decomposition of FeOOH with oleic acid as surfactant and 1 -octadecene as solvent. The influence of oleic acid and FeCl3 content, reaction time on the size and morphology of Fe3O4nanocrystals are studied. The results demonstrate that both the prolonging of reaction time and the increasing of FeCl3content can enlarge the magnetite particles. By increasing the oleic acid from 13. 5 mL to 20 mL, the particle diameter first decreases and then increases. X-ray powder diffraction (XRD) and transmission electron microscopy ( TEM) are used to characterize the structure and morphology of the products. The results reveal that the prepared Fe3O4nanoparticles have an inverse spinel structure. The nanoparticles have high crystallinity, good dispersion and small average diameter can be obtained after reaction at 230 ℃ for 12 with 0. 003 mol FeCl3 and 13. 5 mL oleic acid.%通过溶剂热法,以FeOOH作为前驱体,以油酸作为表面活性剂,以十八烯为溶剂,制备了纳米Fe3O4颗粒,研究了油酸和FeCl3用量、反应时间对纳米Fe3 O4粒子的大小以及分散性的影响.结果显示,FeCl3用量的增加和反应时间的延长均可使Fe3O4粒子粒径增大,油酸用量的增加会导致Fe3O4粒子粒径先减小再增大.利用XRD、TEM等手段对所制备颗粒的结构、形貌进行了表征,结果表明,所制备的纳米Fe3O4粒子属于反尖晶石结构.FeCl3用量为0.003 mol,油酸用量为13.5 mL时(即Fe3+/油酸约为1/15),在230℃反应12 h得到结晶度较高,分散性良好,平均粒径比较小的纳米Fe3O4粒子.

  17. Preparation and enhanced properties of Fe3O4 nanoparticles reinforced polyimide nanocomposites

    Science.gov (United States)

    Ding, Daowei; Yan, Xingru; Zhang, Xi; He, Qingliang; Qiu, Bin; Jiang, Dawei; Wei, Huige; Guo, Jiang; Umar, Ahmad; Sun, Luyi; Wang, Qiang; Khan, Mojammel A.; Young, David P.; Zhang, Xin; Weeks, Brandon; Ho, Thomas C.; Guo, Zhanhu; Wei, Suying

    2015-09-01

    Polyimide (PI) nanocomposite reinforced with Fe3O4 nanoparticles (NPs) at various NPs loadings levels of 5.0, 10.0, 15.0, and 20.0 wt% were prepared. The chemical interactions of the Fe3O4 NPs/PI nanocomposites were characterized using Fourier Transform Infrared (FT-IR) spectroscopy. X-ray Diffraction (XRD) results revealed that the addition of NPs had a significant effect on the crystallization of PI. Scanning electron microscope (SEM) and the atomic force microscope (AFM) were used to characterize the dispersion and surface morphology of the Fe3O4 NPs and the PI nanocomposites. The obtained optical band gap of the nanocomposites characterized using Ultraviolet-Visible Diffuse Reflectance Spectroscopy (UV-Vis DRS) was decreased with increasing the Fe3O4 loading. Differential scanning calorimetry (DSC) results showed a continuous increase of Tg with increasing the Fe3O4 NPs loading. Some differences were observed in the onset decomposition temperature between the pure PI and nanocomposites since the NPs and the PI matrix were physically entangled together to form the nanocomposites. The contact angle of pure PI was larger than that of Fe3O4/PI nanocomposites films, and increased with increasing the loading of Fe3O4. The degree of swelling was increased with increasing the Fe3O4 loading and the swelling time. The dielectric properties of the nanocomposite were strongly related to the Fe3O4 loading levels. The Fe3O4/PI magnetic property also had been improved with increasing the loading of the magnetic nanoparticles.

  18. Synthesis of superparamagnetic Fe3O4/PMMA/SiO2 nanorattles with periodic mesoporous shell for lysozyme adsorption

    Science.gov (United States)

    Lan, Fang; Hu, Hao; Jiang, Wen; Liu, Kexia; Zeng, Xiaobo; Wu, Yao; Gu, Zhongwei

    2012-03-01

    A new kind of nanorattle, composed of a Fe3O4/polymethyl methacrylate (PMMA) composite nanospherical core and mesoporous SiO2 shell, has been successfully synthesized with the combination of a modified stöber method and a dual-template strategy, followed by alcohol dialysis. The nanorattles showed high efficiency in protein adsorption and separation.A new kind of nanorattle, composed of a Fe3O4/polymethyl methacrylate (PMMA) composite nanospherical core and mesoporous SiO2 shell, has been successfully synthesized with the combination of a modified stöber method and a dual-template strategy, followed by alcohol dialysis. The nanorattles showed high efficiency in protein adsorption and separation. Electronic supplementary information (ESI) available: Experimental details, SAXRD pattern. See DOI: 10.1039/c2nr12125e

  19. One-pot sequential synthesis of magnetically separable Fe3O4/AgCl photocatalysts with enhanced activity and stability

    Science.gov (United States)

    Liu, Zening; Liu, Yongcheng; Cai, Mujin; Xu, Piaopiao; Ma, Zonghua; Yuan, Hong

    2017-03-01

    Magnetically separable Fe3O4/AgCl photocatalysts were prepared by a one-pot sequential method. A series of techniques proved the hybrid structure of Fe3O4/AgCl composites. Fe3O4/AgCl composites had a much higher photocatalytic activity toward Rhodamine B (RhB) degradation than pure AgCl under the simulated solar light irradiation. The existence of metal Ag resulted in high photocatalytic activity of Fe3O4/AgCl, which was related with the amount of metallic Ag. The scavenging experiments showed that the degradation reaction most probably was initiated by the photoinduced single-electron transfer, and the generation of superoxide anion (O 2 -· ) played a significant role. The composite photocatalysts could be recycled by applying an external magnetic field, and the reused composites maintained their original photocatalytic activity. Fe3O4/AgCl composites were highly efficient, magnetically separable, and recoverable. This proves their potential applications in the photodegradation of organic pollutants.

  20. One-Pot Synthesis of Bi/Fe3O4 and Its Catalytic Performances for 4-Nitrophenol Reduction

    Directory of Open Access Journals (Sweden)

    Ke-ying Cai

    2017-04-01

    Full Text Available A novel approach was successfully developed for the catalyst Bi-deposited Fe3O4 magnetic nanoparticles, which was used in the degradation of 4-nitrophenol (4-NP. The Bi/Fe3O4 composite was prepared via a one-pot process from ferrous sulfate and bismuth chloride using hydrazine hydrate as a reducing agent. The catalyst was characterized by X-ray diffraction (XRD and Fourier transform infrared (FTIR spectroscopy. In the composite pure Fe3O4 particles were synthesized and bismuth particles were well dispersed. The catalytic performances were investigated for the reduction of 4-NP with sodium borohydride. The catalyst has higher activity when Bi/Fe molar ratio is 1:4 in the composite and the rate constant k is about 0.611 min-1. The catalyst has good reusability which can be used 10 cycles without obvious deactivation. Furthermore, the catalyst can be easily separated by an external magnetic field. Copyright © 2017 BCREC GROUP. All rights reserved Received: 11st August 2016; Revised: 20th December 2016; Accepted: 21st December 2016 How to Cite: Cai, K.Y., Liu, Y.S., Xu, Y., Zhou, H., Zhang, L., Cui., Y. (2017. One-Pot Synthesis of Bi/Fe3O4 and Its Catalytic Performances for 4-Nitrophenol Reduction. Bulletin of Chemical Reaction Engineering & Catalysis, 12 (1: 89-95 (doi:10.9767/bcrec.12.1.621.89-95 Permalink/DOI: http://dx.doi.org/10.9767/bcrec.12.1.621.89-95

  1. Facile synthesis and enhanced magnetic, photocatalytic properties of one-dimensional Ag@Fe3O4-TiO2

    Science.gov (United States)

    Jia, Xiaohua; Dai, Rongrong; Lian, Dandan; Han, Song; Wu, Xiangyang; Song, Haojie

    2017-01-01

    Fe3O4-TiO2 heterostructures were synthesized through co-precipitation method based on TiO2 nanobelts. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), vibration sample magnetometry (VSM) were used to characterize the heterostructure nanocomposites. The results of XRD proved that the TiO2 nanobelt was anatase which was the most suitable crystal form for photocatalysis. SEM and TEM analysis indicated that Fe3O4 nanoparticles were adhere to TiO2 nanobelts which have one-dimensional structure with 100-200 nm in width. The VSM measurements showed that the photocatalyst can be easily recovered by an extemal magnetic field. X-ray photoelectron spectroscopy (XPS) of Ag@Fe3O4-TiO2 nanocomposites studies confirm that Ag is in Ag0 state. Finally, the photodegradation of rhodamine B (RhB) by the obtained magnetic photocatalyst was investigated via UV-vis absorption spectra. The photocatalytic activity of the composites was observed to be lower compared to bare TiO2 due to the higher degree of recombination reactions after combined with Fe3O4 nanoparticles. After coated the composite of 15% Fe3O4-TiO2 with Ag, the new nanocomposite of Ag@Fe3O4-TiO2 can be easily recovered after photocatalysis by an extemal magnetic field and showed enhanced photocatalytic activity. The mechanisms for the exhibited enhanced photocatalytic effect of Ag nanoparticle decorated Fe3O4-TiO2 nanocomposites with surface heterostructures are discussed.

  2. A simple way to prepare Au@polypyrrole/Fe3O4 hollow capsules with high stability and their application in catalytic reduction of methylene blue dye

    Science.gov (United States)

    Yao, Tongjie; Cui, Tieyu; Wang, Hao; Xu, Linxu; Cui, Fang; Wu, Jie

    2014-06-01

    Metal nanoparticles are promising catalysts for dye degradation in treating wastewater despite the challenges of recycling and stability. In this study, we have introduced a simple way to prepare Au@polypyrrole (PPy)/Fe3O4 catalysts with Au nanoparticles embedded in a PPy/Fe3O4 capsule shell. The PPy/Fe3O4 capsule shell used as a support was constructed in one-step, which not only dramatically simplified the preparation process, but also easily controlled the magnetic properties of the catalysts through adjusting the dosage of FeCl2.4H2O. The component Au nanoparticles could catalyze the reduction of methylene blue dye with NaBH4 as a reducing agent and the reaction rate constant was calculated through the pseudo-first-order reaction equation. The Fe3O4 nanoparticles permitted quick recycling of the catalysts with a magnet due to their room-temperature superparamagnetic properties; therefore, the catalysts exhibited good reusability. In addition to catalytic activity and reusability, stability is also an important property for catalysts. Because both Au and Fe3O4 nanoparticles were wrapped in the PPy shell, compared with precursor polystyrene/Au composites and bare Fe3O4 nanoparticles, the stability of Au@PPy/Fe3O4 hollow capsules was greatly enhanced. Since the current method is simple and flexible to create recyclable catalysts with high stability, it would promote the practicability of metal nanoparticle catalysts in industrial polluted water treatment.Metal nanoparticles are promising catalysts for dye degradation in treating wastewater despite the challenges of recycling and stability. In this study, we have introduced a simple way to prepare Au@polypyrrole (PPy)/Fe3O4 catalysts with Au nanoparticles embedded in a PPy/Fe3O4 capsule shell. The PPy/Fe3O4 capsule shell used as a support was constructed in one-step, which not only dramatically simplified the preparation process, but also easily controlled the magnetic properties of the catalysts through adjusting

  3. Characteristics of magnetic Fe3O4 nanoparticles encapsulated with human serum albumin

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    Magnetic nanoparticles (Fe3O4) were prepared by chemical precipitation method using Fe2+ and Fe3+salts with sodium hydroxide in the nitrogen atmosphere. Fe3O4 nanoparticles were coated with human serum albumin(HSA) for magnetic resonance imaging as contrast agent. Characteristics of magnetic particles coated or uncoated were carried out using scanning electron microscopy and X-ray diffraction. Zeta potentials, package effects and distributions of colloid particles were measured to confirm the attachment of HSA on magnetic particles. Effects of Fe3O4 nanoparticles coated with HSA on magnetic resonance imaging were investigated with rats. The experimental results show that the adsorption of HSA on magnetic particles is very favorable to dispersing of magnetic Fe3O4 particles, while the sizes of Fe3O4 particles coated are related to the molar ratio of Fe3O4 to HSA. The diameters of the majority of particles coated are less than 100 nm. Fe3O4 nanoparticle coated with HSA has a good biocompatibility and low toxicity. This new contrast agent has some effects on the nuclear magnetic resonance imaging of liver and the lowest dosage is 20 μmol/kg for the demands of diagnosis.

  4. Improving Pullulanase Catalysis via Reversible Immobilization on Modified Fe3O4@Polydopamine Nanoparticles.

    Science.gov (United States)

    Wang, Jianfeng; Liu, Zhongmei; Zhou, Zhemin

    2017-08-01

    To improve the catalysis of pullulanase from Anoxybacillus sp.WB42, Fe3O4@polydopamine nanoparticles (Fe3O4@PDA) were prepared and modified with functional groups for immobilization of pullulanases via covalent binding or ionic adsorption. Immobilized pullulanases had lower thermal stability than that of free pullulanase, whereas their catalysis depended on the surface characteristics of nanoparticles. As for covalent immobilization of pullulanases onto Fe3O4@PDA derivatives, the spacer grafted onto Fe3O4@PDA made the catalytic efficiency of pullulanase increase up to the equivalence of free enzyme but dramatically reduced the pullulanase thermostability. In contrast, pullulanases bounded ionically to Fe3O4@PDA derivatives had higher activity recovery and catalytic efficiency, and their catalytic behaviors varied with the modifier grafted onto Fe3O4@PDA. Among these immobilized pullulanases, ionic adsorption of pullulanase on Fe3O4@PDA-polyethyleneimine-glycidyltrimethylammonium gave a high-performance and durable catalyst, which displayed not only 1.5-fold increase in catalytic efficiency compared to free enzyme but also a significant improvement in operation stability with a half of initial activity after 27 consecutive cycles with a total reaction time of 13.5 h, and was reversible, making this nanoparticle reusable for immobilization.

  5. Superior Antibacterial Activity of Fe3O4-TiO2 Nanosheets under Solar Light.

    Science.gov (United States)

    Ma, Shuanglong; Zhan, Sihui; Jia, Yanan; Zhou, Qixing

    2015-10-07

    Fe3O4-TiO2 nanosheets (Fe3O4-TNS) were synthesized by means of lamellar reverse micelles and solvothermal method, which were characterized by TEM, XRD, XPS, BET, and magnetic property analysis. It can be found that Fe3O4-TNS nanosheets exhibited better photocatalytic antibacterial activity toward Gram-negative Escherichia coli and Gram-positive Staphylococcus aureus than pure Fe3O4 and TNS, and the antibacterial efficiency could reach 87.2% and 93.7% toward E. coli and S. aureus with 100 μg/mL Fe3O4-TNS after 2 h of simulated solar light illumination, respectively. The photocatalytic destruction of bacteria was further confirmed by fluorescent-based cell live/dead test and SEM images. It was uncovered that Fe3O4-TNS inactivated G- E. coli and G+ S. aureus by different mechanisms: the destruction of outer membranes and ruptured cell bodies were responsible for the bactericidal effect against E. coli, while the antibacterial effect toward S. aureus were due to the fact that the cells were adsorbed in form of clusters by massive Fe3O4-TNS, which could restrict their activities and cause malfunction of the selective permeable barriers. Furthermore, the antibacterial mechanism was studied by employing scavengers to understand exact roles of different reactive species, indicating the key roles of h(+) and H2O2. The recovery and reusability experiments indicated that Fe3O4-TNS still retained more than 90% bacteria removal efficiency even after five cycles. Considering the easy magnetic separation, bulk availability, and high antibacterial activity of Fe3O4-TNS, it is a promising candidate for cleaning the microbial contaminated water environment.

  6. Fe3O4 nano-whiskers by ultrasonic-aided reduction in concentrated NaOH solution

    Institute of Scientific and Technical Information of China (English)

    Chenglong Yu; Xin Hao; Hongtao Jiang; Lili Wang

    2011-01-01

    Fe3O4 nano-whiskers were synthesized via ultrasonic-aided reduction of FeCl2·4H2O with N2H4·H2O in concentrated NaOH solution. Phase identification and morphology observation were conducted by X-ray diffraction (XRD) analysis,transmission electron microscopy (TEM) and field emission scanning electron microscopy (FE-SEM). Face scanning energy dispersive spectrum (face scanning EDS) and two-dimensional fast Fourier transform (2DFFT) for element distribution were carried out for confirming composition homogeneity. From XRD and TEM,the synthesized Fe3O4 nano-whiskers are of cubic phase with average dimension of 20 nm × 200 nm (average aspect ratio of 10). FE-SEM shows that the nanowhiskers without dispersion are interconnected into a network at a scale of 20μm. 2DFFT of the distribution of Fe and O from face scanning EDS confirms the composition homogeneity of the synthesized Fe3O4. Hydrazine hydrate determines the formation of the nano-whiskers,while the possible mechanism is the preferred growth along certain orientation with the aid of ultrasonic treatment.

  7. A simple way to prepare Au@polypyrrole/Fe3O4 hollow capsules with high stability and their application in catalytic reduction of methylene blue dye.

    Science.gov (United States)

    Yao, Tongjie; Cui, Tieyu; Wang, Hao; Xu, Linxu; Cui, Fang; Wu, Jie

    2014-07-07

    Metal nanoparticles are promising catalysts for dye degradation in treating wastewater despite the challenges of recycling and stability. In this study, we have introduced a simple way to prepare Au@polypyrrole (PPy)/Fe3O4 catalysts with Au nanoparticles embedded in a PPy/Fe3O4 capsule shell. The PPy/Fe3O4 capsule shell used as a support was constructed in one-step, which not only dramatically simplified the preparation process, but also easily controlled the magnetic properties of the catalysts through adjusting the dosage of FeCl2·4H2O. The component Au nanoparticles could catalyze the reduction of methylene blue dye with NaBH4 as a reducing agent and the reaction rate constant was calculated through the pseudo-first-order reaction equation. The Fe3O4 nanoparticles permitted quick recycling of the catalysts with a magnet due to their room-temperature superparamagnetic properties; therefore, the catalysts exhibited good reusability. In addition to catalytic activity and reusability, stability is also an important property for catalysts. Because both Au and Fe3O4 nanoparticles were wrapped in the PPy shell, compared with precursor polystyrene/Au composites and bare Fe3O4 nanoparticles, the stability of Au@PPy/Fe3O4 hollow capsules was greatly enhanced. Since the current method is simple and flexible to create recyclable catalysts with high stability, it would promote the practicability of metal nanoparticle catalysts in industrial polluted water treatment.

  8. Adsorption of Acid Red 114 onto Fe3O4@Caffeic acid recycable magnetic nanocomposite

    OpenAIRE

    YILDIZ, Aylin

    2016-01-01

    In this study, the adsorption capacity of caffeic acid (CFA) functionalized Fe3O4 magnetic recyclable nanocomposite (Fe3O4@CFA MNCs) for removal of industrial dye Acid Red 114 (AR 114) was investigated. The max. adsorption (qm) of the Fe3O4@CFA MNCs for AR114 was 333 mg/g without pH correction of the solution. Compared with other studies these adsorbent possess very adsorption capacity for AR114 dye. The adsorption isotherm data and the process of adsorption kinetics were fitted using the Lan...

  9. Pharmacokinetic parameters and tissue distribution of magnetic Fe3O4 nanoparticles in mice

    Directory of Open Access Journals (Sweden)

    Jun Wang

    2010-10-01

    Full Text Available Jun Wang1, Yue Chen1, Baoan Chen1, Jiahua Ding1, Guohua Xia1, Chong Gao1, Jian Cheng1, Nan Jin1, Ying Zhou1, Xiaomao Li1, Meng Tang2, Xue Mei Wang21Department of Hematology, Zhongda Hospital, Clinical Medical School, Southeast University, Nanjing, People’s Republic of China; 1Department of Physics, University of Saarland, D-266041 Saarbruechen, Germany; 2National Key Laboratory of Bioelectronics (Chien-Shiung Wu Laboratory, Southeast University, Nanjing, People’s Republic of ChinaBackground: This study explored the pharmacokinetic parameters and tissue distribution of magnetic iron oxide nanoparticles (Fe3O4 MNPs in imprinting control region (ICR mice.Methods: The Fe3O4 MNPs were synthesized by chemical coprecipitation, and their morphology and appearance were observed by transmission electron microscopy. ICR mice were divided into a control group and a Fe3O4 MNP-treated group. Probable target organs in ICR mice were observed, and the pharmacokinetic parameters and biodistribution of Fe3O4 MNPs in tissues were identified using atomic absorption spectrophotometry.Results: Fe3O4 MNPs were spherical with a well distributed particle diameter, and were distributed widely in various target organs and tissues including the heart, liver, spleen, lungs, kidneys, brain, stomach, small intestine, and bone marrow. The majority of Fe3O4 MNPs were distributed to the liver and the spleen. Fe3O4 MNP levels in brain tissue were higher in the Fe3O4 MNP-treated group than in the control group, indicating that Fe3O4 MNPs can penetrate the blood–brain barrier.Conclusion: These results suggest that the distribution of Fe3O4 MNPs was mostly in the liver and spleen, so the curative effect of these compounds could be more pronounced for liver tumors. Furthermore, Fe3O4 MNPs might be used as drug carriers to overcome physiologic barriers.Keywords: magnetic nanoparticles, Fe3O4, tissue distribution, mice

  10. Size-dependent peroxidase-like catalytic activity of Fe3O4 nanoparticles

    Institute of Scientific and Technical Information of China (English)

    Fang Fang Peng; Yu Zhang; Ning Gu

    2008-01-01

    Peroxidase-like catalytic properties of Fe3O4 nanoparticles (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.

  11. Carboxymethyl-cellulose/Fe3O4 nanostructures for antimicrobial substances delivery.

    Science.gov (United States)

    Vlad, Mihaela; Andronescu, Ecaterina; Grumezescu, Alexandru Mihai; Ficai, Anton; Voicu, Georgeta; Bleotu, Coralia; Chifiriuc, Mariana Carmen

    2014-01-01

    The synthesis of carboxymethyl-cellulose/magnetite (CMC/Fe3O4) was carried out. This magnetic hybrid material was characterized by infrared spectroscopy, scanning electron microscopy and X-ray diffractometry. The adsorption of norfloxacin and cefotaxim antimicrobial substances (ATB) onto the CMC/Fe3O4 was performed in order to investigate the capacity of the magnetic scaffold to improve the antimicrobial activity of the respective therapeutic agents, assessed by an in vitro quantitative assay. The obtained results proved that CMC/Fe3O4/ATBs might be a promising candidate for the development of efficient and cheap antimicrobial drugs carriers under magnetic field.

  12. A Facile Solvothermal Synthesis of Octahedral Fe3O4 Nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Ooi, Frances; DuChene, Joseph S.; Qiu, Jianqing; Graham, Jeremy O.; Engelhard, Mark H.; Cao, Guixin; Gai, Zheng; Wei, Wei

    2015-06-01

    Magnetic nanoparticles are of great technological interest because they promise numerous potential opportunities in biomedicine and data storage. Although intriguing, these applications require exquisite control over nanostructure morphology in order to appropriately harness their magnetic properties. Most synthesis strategies reported to date are unable to routinely produce anisotropic Fe3O4 nanostructures with appropriate sizes to enable integration into biological systems. Here, we report a simple solvothermal synthesis for obtaining octahedral Fe3O4 nanoparticles with suitable sizes for cellular internalization. Furthermore, these ferromagnetic Fe3O4 octahedrons exhibit substantial saturation magnetization with minimal remanence, suggesting their potential applicability for a host of biomedical applications.

  13. Synthesis and electrochemical properties of Fe3O4@MOF core-shell microspheres as an anode for lithium ion battery application

    Science.gov (United States)

    Sun, Xuemin; Gao, Ge; Yan, Dongwei; Feng, Chuanqi

    2017-05-01

    The Fe3O4@MOF composite with a microspheric core and a porous metal-organic framework (MOF HKUST-1) shell has been successfully synthesized utilizing a versatile Layer-by-Layer (LBL) assembly method. The structure was identified by X-ray diffraction (XRD), and the morphology was investigated by scanning electron microscopy (SEM) and transmission electron microscopy (TEM) techniques. The Fe3O4@MOF composite exhibited outstanding electrochemical properties when it was used as an anode material for lithium ion batteries (LIBs). After 100 discharge-charge cycles at a current density of 100 mA g-1, the reversible capacity of Fe3O4@MOF could maintain ∼1002 mAh g-1, which was much higher than that of the bare Fe3O4 counterpart (696 mAh g-1). Moreover, load the current density as high as 2 A g-1 (after 70 cycles at the current density step increased from 0.1 to 2 A g-1), it still delivered a reversible capacity of ∼429 mAh g-1. The results demonstrate that the cycling stability of Fe3O4 as an anode could be significantly improved by coating Cu3(1,3,5-benzenetricarboxylate)2 (HKUST-1). This strategy may offer new route to prepare other composite materials using different particles and suitable Metal-organic frameworks (MOFs) for LIBs application.

  14. Synthesis of Fe3O4@phenol formaldehyde resin core-shell nanospheres loaded with Au nanoparticles as magnetic FRET nanoprobes for detection of thiols in living cells.

    Science.gov (United States)

    Yang, Ping; Xu, Qi-Zhi; Jin, Sheng-Yu; Zhao, Yang; Lu, Yang; Xu, Xue-Wei; Yu, Shu-Hong

    2012-01-23

    A magnetic, sensitive, and selective fluorescence resonance energy transfer (FRET) probe for detection of thiols in living cells was designed and prepared. The FRET probe consists of an Fe(3)O(4) core, a green-luminescent phenol formaldehyde resin (PFR) shell, and Au nanoparticles (NPs) as FRET quenching agent on the surface of the PFR shell. The Fe(3)O(4) NPs were used as the core and coated with green-luminescent PFR nanoshells by a simple hydrothermal approach. Au NPs were then loaded onto the surface of the PFR shell by electric charge absorption between Fe(3)O(4)@PFR and Au NPs after modifying the Fe(3)O(4)@PFR nanocomposites with polymers to alter the charge of the PFR shell. Thus, a FRET probe can be designed on the basis of the quenching effect of Au NPs on the fluorescence of Fe(3)O(4)@PFR nanocomposites. This magnetic and sensitive FRET probe was used to detect three kinds of primary biological thiols (glutathione, homocysteine, and cysteine) in cells. Such a multifunctional fluorescent probe shows advantages of strong magnetism for sample separation, sensitive response for sample detection, and low toxicity without injury to cellular components.

  15. Fabrication of one-dimensional Fe3O4/P(GMA-DVB) nanochains by magnetic-field-induced precipitation polymerization.

    Science.gov (United States)

    Ma, Mingliang; Zhang, Qiuyu; Dou, Jinbo; Zhang, Hepeng; Yin, Dezhong; Geng, Wangchang; Zhou, Yanyang

    2012-05-15

    One-dimensional (1D) magnetic Fe(3)O(4)/P(GMA-DVB) peapod-like nanochains have been successfully synthesized by magnetic-field-induced precipitation polymerization using Fe(3)O(4) as building blocks and P(GMA-DVB) as linker. The Fe(3)O(4) microspheres without surface modification can be arranged with the direction of the external magnetic field in a line via the dipolar interaction between Fe(3)O(4) microspheres and linked permanently via P(GMA-DVB) coating during precipitation polymerization. The length of peapod-like nanochains can be controlled by magnetic field intensity, and the thickness of polymer shell can be tuned by the amount of monomers. Magnetic measurement revealed that these 1D peapod-like nanochains showed highly magnetic sensitivity. In the presence of magnetic field, 1D magnetic Fe(3)O(4)/P(GMA-DVB) peapod-like nanochains can be oriented and aligned along the direction of external magnetic field.

  16. Preparation of Fe3O4/TiO2 Mgnetic Ctalyst and Application in Swage Teatment%Fe3O4/TiO2磁性催化剂的制备及在污水治理中的应用

    Institute of Scientific and Technical Information of China (English)

    宋海南; 李国喜; 周建庆; 吴寅子

    2011-01-01

    With nano-Fe3O4 as carrier, Fe3O4/TiO2 nanocomposite was synthesized by sol-gel method with tetrabutyl titanate as the precursor. The nanocomposite was charactered by TEM, XRD, XPS, and FTIR, and the results indicate Fe3O4 nanoparticles are wrapped by TiO2. The composite was applied to the treatment of wastewater containing phenolic compounds, and the results indicated that the Fe3O4/TiO2 nanoeomposite shows more excellent photocatalysis activity for degradation of P-Nitrophenol and magnetic recyclability. It is found that UV light up 100 min, the degradation ratio of P-Nitrophenol is 98.6%. and the degradation efficiency up to 86.3% after six times.%以纳米Fe3O4为载体,以钛酸四丁酯为前躯体,用溶胶-凝胶法在Fe3O4表面包覆TiO2层,制备Fe3O4/TiO2光催化材料.透射电镜(TEM)、X射线衍射(XRD)、X射线光电子能谱(XPS)和红外光谱(IR)分析表明,TiO2在纳米Fe3O4颗粒表面形成很好的包覆层.用Fe3O4/TiO2光催化材料对工业上难处理的酚类废水进行处理,结果表明,催化剂的光催化降解活性和磁分离回收性能均较好,光照时间为1.5h,Fe3O4/TiO2可使4-硝基苯酚的降解率达98.6%,Fe3O4/TiO2在重复利用六次后,催化效率仍能达到86.3%.

  17. Preparation of nano Fe3 O4/PS-EDTA microspheres and their adsorption for Cu2+ ion%纳米Fe3O4/PS-EDTA功能微球的制备及对Cu2+的吸附性能

    Institute of Scientific and Technical Information of China (English)

    王华山; 刘玉芳

    2015-01-01

    The nano magnetic composite microspheres(Fe3 O4/PS‐EDTA)were prepared by polymerization and substitution reaction .First ,the Fe3 O4/PS particles were prepared through polymerization of styrene(st) in the surface of Fe3 O4 S.econd ,hydrogen atoms of Fe3 O4/PS were substituted in proper order by chlorine ,ehylenedia‐mine and acetic acid .The synthesized Fe3 O4/PS‐EDTA were characterized by scanning electron microscopy (SEM ) ,X‐ray diffraction ,thermogravimetric (TGA ) analysis ,Fourier transform infrared (FT‐IR) spectrome‐ter and ultraviolet spectrophotometer .Results show that EDTA were effectively connected with chemical bond to the surface of nano‐magnetic Fe3 O4/PS with uniform particle size .The adsorption dynamic process fit the Langmuir isotherms well with a maximum adsorption capacity of 98 5.9 mg/g for Cu2+ and the adsorption kinet‐ics followed the mechanism of the pseudo‐second order equation .%以磁性纳米Fe3 O4为核,利用苯乙烯(St)聚合对其进行包覆,并进一步对表面进行氯取代、乙二胺取代及氯乙酸取代反应,制备了 Fe3 O4/PS‐EDTA 纳米磁性复合微球。利用扫描电子显微镜(SEM )、X射线衍射分析(XRD)、热重(TGA)分析、傅里叶变换红外(FT‐IR)光谱仪、紫外分光光度计等对 Fe3 O4/PS‐EDTA微球性能进行了表征。结果表明,EDTA 有效地以化学键合方式连接到纳米磁性Fe3 O4/PS 表面,且粒径均匀。 Fe3 O4/PS‐EDTA 对 Cu2+表现出了良好的吸附性能,饱和吸附量为98.59 m g/g ,吸附等温数据符合Langmuir模型,吸附动力学符合拟二级反应动力学模型。

  18. Controllable synthesis of magnetic Fe3O4 particles with different morphology by one-step hydrothermal route

    Science.gov (United States)

    Chen, Zhongtao; Du, Yi; Li, Zhongfu; Yang, Kai; Lv, Xingjie

    2017-03-01

    Well-defined Fe3O4 particles were successfully fabricated by a facile triethanolamine (TEA)-assisted method under mild hydrothermal conditions. Hydrated ferric salt was employed as the single iron precursor. TEA was used as the complexing agent and/or alkaline source. The crystalline phases of the as-obtained samples were characterized by X-ray diffraction (XRD). Furthermore, the morphology as well as the compositions of the samples were investigated by scanning electron microscopy (SEM) equipped with an energy dispersion spectroscopy (EDS). The results indicated that the products were Fe3O4 crystal phase, and the morphology and powder size of the particles were varied with adding different amount of NaOAc and keeping the content of TEA unchanged. On the basis of these results, the possible formation mechanism of Fe3O4 was discussed. It was observed that TEA and NaOAc affected the growth rate of crystal planes and nucleation. Besides, the magnetic property tested by a vibrating sample magnetometer (VSM) showed that the products exhibited a ferromagnetic behavior and possessed the excellent saturation magnetization (Ms) at room temperature.

  19. UCST-like hybrid PAAm-AA/Fe3O4 microgels. Effect of Fe3O4 nanoparticles on morphology, thermosensitivity and elasticity.

    Science.gov (United States)

    Echeverria, Coro; Mijangos, Carmen

    2011-07-01

    The incorporation of metal oxide nanoparticles into microgels forming hybrid systems gives additional functionalities to the system and widens the field of potential application in biomedicine, biotechnology, and other fields. In particular, there have been very few investigations regarding UCST-like hybrid microgels. In connection with this, we report the preparation of UCST-like hybrid microgels of magnetite nanoparticles (Fe(3)O(4)) encapsulated in poly(acrylamide-acrylic acid) microgel matrix via an inverse emulsion polymerization method. The key factor in the preparation of hybrid microgels is the need to divide in two the aqueous phase of the emulsion and feed them separately in order to avoid the aggregation of magnetic nanoparticles prior to polymerization reaction. The morphology, size, and spherical shape of hybrid microgels are determined by scanning electron microscopy. The encapsulation of magnetite nanoparticles within the polymer matrix is confirmed by transmission electron microscopy. Dynamic light scattering is employed to study both the swelling UCST-like behavior and the surface charge of the hybrid microgels. Swelling measurements confirm that the incorporation of magnetite does not affect the thermosensitivity of the system. In order to highlight the rheological behavior that can affect the final potential applications of these hybrid systems, a deep study of the viscoelastic properties is carried out by means of an oscillatory rheometer. The dependence of G' and G'' of the microgel dispersions with the frequency suggests a gel-like behavior and hence the occurrence of structural organization. In order to understand this structure formation and the influence of the magnetite in the interaction between hybrid microgels, scaling theory was applied. In terms of rheology, the addition of magnetite leads to a change in the interaction between hybrid microgels giving rise to an increase in the elasticity of the system.

  20. Fe_3O_4磁粉的合成与结构表征%Preparation of Fe3O4 Nanoparticle by Liquid - phase Coprecipitation

    Institute of Scientific and Technical Information of China (English)

    霍涌前; 陈小利; 王升文; 崔华莉; 王潇

    2012-01-01

    Nanometer magnetite Fe3O4 particles were prepared by chemical co -precipitation, NH3·H2O was cho- sen as precipitating agent and added to the mixed aqueous solution containing ferric and ferrous ions to produce nanometer Fe3O4 particles. Some influence factors on the size were investigated. The phase structure of the particle was measured by XRD test, and the average size was about 28 nm.%采用化学共沉淀法制备纳米磁性Fe3O4粒子。选用NH3.H2O作为沉淀剂,加入到Fe2+和Fe3+的混合盐溶液中,制得了纳米磁性Fe3O4粒子。考察了影响产物粒径的一些实验因素。通过X-Ray谱图证实了产物结构特征,平均粒径在37 nm左右,平均晶粒度只有28 nm左右的均分散。

  1. A Study of Fe3O4@ Zigzag, @Armchair and @Chiral Swcnts and α and γ Cyclodextrins

    Directory of Open Access Journals (Sweden)

    Somayeh Khosravi

    2016-08-01

    Full Text Available Fe3O4 is used as a catalyst in the Haber process and in the water gas shift reaction. In this work we have investigated the physical and chemical properties of Fe3O4@ Zigzag, @Armchair and @Chiral SWCNTs compare to Fe3O4@ -Cyclodextrin in view point of chemical reaction and sensitizes. The electrical properties such as NMR Shielding, electron densities, energy densities , potential energy densities, ELF, LOL, ellipticity of electron density , eta index and ECP for Fe3O4@ -Cyclodextrin shell and Fe3O4@ Zigzag, @Armchair and @Chiral SWCNTs have been calculated for the simulations. Our Calculation indicate that the Fe3O4 @ (7, 7 and Fe3O4 @ (10,5 and Fe3O4 @ (9, 0 have physical and chemical properties close to Fe3O4@ -Cyclodextrin and as well as the Fe3O4 @ (8,8 and Fe3O4 @ (11,6 and Fe3O4 @ (10, 0 are close to Fe3O4@ -Cyclodextrin.

  2. TEA controllable preparation of magnetite nanoparticles (Fe3O4 NPs) with excellent magnetic properties

    Science.gov (United States)

    Han, Chengliang; Zhu, Dejie; Wu, Hanzhao; Li, Yao; Cheng, Lu; Hu, Kunhong

    2016-06-01

    A fast and controllable synthesis method for superparamagnetic magnetite nanoparticles (Fe3O4 NPs) was developed in Fe(III)-triethanolamine (TEA) solution. The phase structure, morphology and particle size of the as-synthesized samples were characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM). The results showed that the magnetic particles were pure Fe3O4 with mean sizes of approximately 10 nm. The used TEA has key effects on the formation of well dispersing Fe3O4 NPs. Vibrating sample magnetometer (VSM) result indicated that the as-obtained Fe3O4 NPs exhibited superparamagnetic behavior and the saturation magnetization (Ms) was about 70 emu/g, which had potential applications in magnetic science and technology.

  3. Crystal structures and magnetic properties of magnetite (Fe3O4)/Polyvinyl alcohol (PVA) ribbon

    Science.gov (United States)

    Ardiyanti, Harlina; Suharyadi, Edi; Kato, Takeshi; Iwata, Satoshi

    2016-04-01

    Ribbon of magnetite (Fe3O4)/Polyvinyl Alcohol (PVA) nanoparticles have been successfully fabricated with various concentration of PVA synthesized by co-precipitation method. Particle size of nanoparticles Fe3O4 sample and ribbon Fe3O4/PVA 25% sample is about 9.34 nm and 11.29 nm, respectively. The result of Vibrating Sample Magnetometer (VSM) showed that saturation magnetization value decreased from 76.99 emu/g to 15.01 emu/g and coercivity increased from 49.30 Oe to 158.35 Oe as increasing concentration of PVA. Atomic Force Microscopy (AFM) analysis showed that encapsulated PVA given decreasing agglomeration, controlled shape of nanoparticles Fe3O4 more spherical and dispersed. Surface roughness decreased with increasing concentration of PVA.

  4. Magnetically separable Fe3O4@DOPA–Pd: a heterogeneous catalyst for aqueous Heck reaction

    Data.gov (United States)

    U.S. Environmental Protection Agency — Magnetically separable Fe3O4@DOPA–Pd catalyst has been synthesized via anchoring of palladium over dopamine-coated magnetite via co-ordinate interaction and the...

  5. Synthesis of Fe3O4 nanoparticles and its antibacterial application

    Science.gov (United States)

    Prabhu, Y. T.; Rao, K. Venkateswara; Kumari, B. Siva; Kumar, Vemula Sesha Sai; Pavani, Tambur

    2015-02-01

    The Present work outlines the antibacterial activity of Fe3O4 nanoparticles synthesized through chemical combustion method where ferric nitrate is used as precursor material and urea as fuel with the assistant of Tween 80, a non-ionic surfactant. The obtained Fe3O4 nanoparticles were characterized by X-ray diffraction, differential thermal analysis/thermo gravimetric analysis (DTA/TGA), particle size analyzer, SEM with EDAX and TEM. Various parameters such as dislocation density, micro strain, analysis of weight loss and surface morphological studies were calculated. The particle size was calculated from XRD and it was found to be 33-40 nm. Using well diffusion method antibacterial activity of Fe3O4 nanoparticles was tested against gram-positive and gram-negative Staphylococus aureus, Xanthomonas, Escherichia coli and Proteus vulgaris. Fe3O4 nanoparticles exhibited strong antibacterial activity against bacterial species.

  6. pH controlled release of chromone from chromone-Fe3O4 nanoparticles.

    Science.gov (United States)

    Wang, Baodui; Xu, Chenjie; Xie, Jin; Yang, Zhengyin; Sun, Shouheng

    2008-11-05

    We report a new strategy for coupling chromone to Fe3O4 nanoparticles. The chromone-Fe3O4 NP conjugate shows a dramatic increase in chromone solubility in cell culture medium from less than 2.5 to 633 microg/ml, leading to the enhanced chromone uptake by HeLa cells. Chromone can be released at low pH and as a result, the chromone-Fe3O4 conjugate is much more efficient in inhibiting the HeLa cell proliferation. Such chromone-Fe3O4 NPs are promising as a powerful multifunctional delivery system for both chromone-based diagnostic and therapeutic applications.

  7. Structure and magnetic properties of amorphous and polycrystalline Fe3O4 thin films

    Institute of Scientific and Technical Information of China (English)

    TANG Xiao-li; ZHANG Huai-wu; SU Hua; ZHONG Zhi-yong; JING Yu-lan

    2006-01-01

    Half-metallic Fe3O4 films prepared by DC magnetron reactive sputtering with a tantalum(Ta) buffer layer was investigated. Primary emphasis is placed on the structural impact on its magnetic properties. The experimental results show that the amorphous Fe3O4 films exhibit a superparamagnetic response at a large-scale from 20 nm to 150 nm,and the magnetoresistance (MR) isn't detected. By contrast,the polycrystalline Fe3O4 films possess large saturation magnetization Ms of 420 A/(kg-cm) and a clear magnetoresistance with a field of 40 kA/m. The unusual properties for the amorphous Fe3O4 film are attributed to the existing large density of the similar structure as anti-phase boundaries in the film.

  8. Assembly of Fe3O4 nanoparticles on SiO2 monodisperse spheres

    Indian Academy of Sciences (India)

    K C Barick; D Bahadur

    2006-11-01

    The assembly of superparamagnetic Fe3O4 nanoparticles on submicroscopic SiO2 spheres have been prepared by an in situ reaction using different molar ratios of Fe3+/Fe2+ (50–200%). It has been observed that morphology of the assembly and properties of these hybrid materials composed of SiO2 as core and Fe3O4 nanoparticles as shell depend on the molar ratio of Fe3+/Fe2+.

  9. Removal of Microcystis aeruginosa using nano-Fe3O4 particles as a coagulant aid.

    Science.gov (United States)

    Zhang, Bo; Jiang, Dan; Guo, Xiaochen; He, Yiliang; Ong, Choon Nam; Xu, Yongpeng; Pal, Amrita

    2015-12-01

    Blue-green algae bloom is of great concern globally since they adversely affect the water ecosystem and also drinking water treatment processes. This work investigated the removal of Microcystis aeruginosa (M. aeruginosa) by combining the conventional coagulant polyaluminum chloride (PACl) with nano-Fe3O4 particles as a coagulant aid. The results showed that the addition of nano-Fe3O4 significantly improved the removal efficiency of M. aeruginosa by reducing the amount of PACl dosage and simultaneously hastening the sedimentation. At the M. aeruginosa density of an order of magnitude of 10(7), 10(6), and 10(5) pcs/mL, respectively, the corresponding PACl dose of 200, 20, and 2 mg/L and the mass ratio of PACl to nano-Fe3O4 of 4:1, the removal efficiency of M. aeruginosa could be increased by 33.0, 44.7, and 173.1%, respectively. Compared to PACl, PACl combined with the nano-Fe3O4 as a coagulant aid had higher removal efficiency at a wider pH range. SEM images showed that nano-Fe3O4 first combined with PACl to form clusters and further generated the flocs with algae. Results from the laser particle analyzer further suggested that the floc size increased with the addition of nano-Fe3O4. It was noted that the addition of nano-Fe3O4 led to aluminum species change after PACl hydrolyzed in the algae solution, from Ala to Alb and Alc subsequently. As a coagulant aid, the nano-Fe3O4, in conjunction with PACl, apparently provided nucleation sites for larger flocs to integrate with M. aeruginosa. In addition, increased floc density improved the removal of M. aeruginosa.

  10. Multifunctional Fe3O4 @ Au core/shell nanostars: a unique platform for multimode imaging and photothermal therapy of tumors

    Science.gov (United States)

    Hu, Yong; Wang, Ruizhi; Wang, Shige; Ding, Ling; Li, Jingchao; Luo, Yu; Wang, Xiaolin; Shen, Mingwu; Shi, Xiangyang

    2016-06-01

    We herein report the development of multifunctional folic acid (FA)-targeted Fe3O4 @ Au nanostars (NSs) for targeted multi-mode magnetic resonance (MR)/computed tomography (CT)/photoacoustic (PA) imaging and photothermal therapy (PTT) of tumors. In this present work, citric acid-stabilized Fe3O4/Ag composite nanoparticles prepared by a mild reduction route were utilized as seeds and exposed to the Au growth solution to induce the formation of Fe3O4 @ Au core/shell NSs. Followed by successive decoration of thiolated polyethyleneimine (PEI-SH), FA via a polyethylene glycol spacer, and acetylation of the residual PEI amines, multifunctional Fe3O4 @ Au NSs were formed. The designed multifunctional NSs possess excellent colloidal stability, good cytocompatibility in a given concentration range, and specific recognition to cancer cells overexpressing FA receptors. Due to co-existence of Fe3O4 core and star-shaped Au shell, the NSs can be used for MR and CT imaging of tumors, respectively. Likewise, the near infrared plasmonic absorption feature also enables the NSs to be used for PA imaging and PTT of tumors. Our study clearly demonstrates a unique theranostic nanoplatform that can be used for high performance multi-mode imaging-guided PTT of tumors, which may be extendable for theranostics of different diseases in translational medicine.

  11. Graphene/Fe3 O4 Nanocomposites as Efficient Anodes to Boost the Lifetime and Current Output of Microbial Fuel Cells.

    Science.gov (United States)

    Song, Rong-Bin; Zhao, Cui-E; Gai, Pan-Pan; Guo, Dan; Jiang, Li-Ping; Zhang, Qichun; Zhang, Jian-Rong; Zhu, Jun-Jie

    2017-02-01

    The enhancement of microbial activity and electrocatalysis through the design of new anode materials is essential to develop microbial fuel cells (MFCs) with longer lifetimes and higher output. In this research, a novel anode material, graphene/Fe3 O4 (G/Fe3 O4 ) composite, has been designed for Shewanella-inoculated MFCs. Because the Shewanella species could bind to Fe3 O4 with high affinity and their growth could be supported by Fe3 O4 , the bacterial cells attached quickly onto the anode surface and their long-term activity improved. As a result, MFCs with reduced startup time and improved stability were obtained. Additionally, the introduction of graphene not only provided a large surface area for bacterial attachment, but also offered high electrical conductivity to facilitate extracellular electron transfer (EET). The results showed that the current and power densities of a G/Fe3 O4 anode were much higher than those of each individual component as an anode.

  12. Green Synthesis of Magnetite (Fe3O4) Nanoparticles Using Seaweed ( Kappaphycus alvarezii) Extract

    Science.gov (United States)

    Yew, Yen Pin; Shameli, Kamyar; Miyake, Mikio; Kuwano, Noriyuki; Bt Ahmad Khairudin, Nurul Bahiyah; Bt Mohamad, Shaza Eva; Lee, Kar Xin

    2016-06-01

    In this study, a simple, rapid, and eco-friendly green method was introduced to synthesize magnetite nanoparticles (Fe3O4-NPs) successfully. Seaweed Kappaphycus alvarezii ( K. alvarezii) was employed as a green reducing and stabilizing agents. The synthesized Fe3O4-NPs were characterized with X-ray diffraction (XRD), ultraviolet-visible spectroscopy (UV-Vis), Fourier transform infrared (FT-IR), and transmission electron microscopy (TEM) techniques. The X-ray diffraction planes at (220), (311), (400), (422), (511), (440), and (533) were corresponding to the standard Fe3O4 patterns, which showed the high purity and crystallinity of Fe3O4-NPs had been synthesized. Based on FT-IR analysis, two characteristic absorption peaks were observed at 556 and 423 cm-1, which proved the existence of Fe3O4 in the prepared nanoparticles. TEM image displayed the synthesized Fe3O4-NPs were mostly in spherical shape with an average size of 14.7 nm.

  13. Inductive heat property of Fe3O4 nanoparticles in AC magnetic field for local hyperthermia

    Institute of Scientific and Technical Information of China (English)

    ZHAO Donglin; ZENG Xianwei; XIA Qisheng; TANG Jintian

    2006-01-01

    Magnetite (Fe3O4) nanoparticles with different magnetic properties were prepared by coprecipitation of Fe3+ and Fe2+ with aqueous NaOH solution.The inductive heat properties of Fe3O4 nanoparticles in an alternating current (AC) magnetic field were investigated for local hyperthermia. The maximum saunder the optimum conditions of Fe3+:Fe2+ molar ratio at 1.8:1. The Ms of Fe3O4 nanoparticles decreased as the Fe3+ /Fe2+ molar ratio increased. But the coercivity Hc increases with the increasing of Fe3+ /Fe2+ molar ratio. Exposed in the AC magnetic field for 29 min, the temperatures of physiological saline suspension containing Fe3O4 nanoparticles were 42-97.5 ℃.The inductive heat property of Fe3O4 nanoparticles in AC magnetic field decreases as Hc increases, but increases with the increasing of Ms. The Fe3O4 nanoparticles would be useful as good thermoseeds for localized hyperthermia treatment of cancers.

  14. Cytotoxicity and genotoxicity of GO-Fe3O4 hybrid in cultured mammalian cells

    Directory of Open Access Journals (Sweden)

    Jedrzejczak-Silicka Magdalena

    2017-03-01

    Full Text Available The study was aimed at investigating the effect of the Fe3O4 hybrid deposited on graphene oxide (GO-Fe3O4 on the relative viability and DNA integrity. The properties of the GO-Fe3O4 hybrid were analyzed using a transmission electron microscopy (TEM, X-ray diffraction technique (XRD and thermal gravimetric method (TGA, while the efficiency of graphene oxide covalent functionalization with iron oxide nanospheres was determined by Fourier transform infrared spectroscopy (FT-IR. L929 and MCF-7 cell lines were selected to analyze the biocompatibility of GO-Fe3O4 nanoparticles. The hybrid was tested using WST-1 and LDH leakage assays. DNA integrity was analyzed by agarose gel electrophoresis and micronucleus assay was performed to examine chromosomal damage in the exposed cell lines. The tested GO-Fe3O4 hybrid did not significantly reduce cell metabolism of L929 cells. GO-Fe3O4 hybrid particles only slightly affected the integrity of cell membranes. DNA integrity and micronucleus assays did not indicate genotoxicity of the hybrid.

  15. Removal of Cr(VIin water by Fe3O4/IP6

    Directory of Open Access Journals (Sweden)

    CHEN Lu

    2014-12-01

    Full Text Available The preparation of functional ferroferric oxide (Fe3O4 magnetic nanoparticles is widely concerned.However,during their preparation,it is difficult to control the morphology of Fe3O4 nanoparticles and also a serious agglomeration exists,greatly restricting their applications.In present paper,an economical and ′green′ reagent-phytic acid (IP6 can form micelle in the water and then the nanoparticles can grow in a soft template.The as-prepared Fe3O4/IP6 exhibited a good stability and high dispersion.Fe3O4/IP6 can chelate with Cr (VI due to its phosphate structure.The Fe3O4/IP6 chelated with Cr (VI can be removed conveniently from water using an external magnet.Fe3O4/IP6 nanocomposites have a good adsorption capacity to Cr (VI within a short time (10 min.Additionally,the effect of pH on adsorption efficiency was studied.

  16. Growth mechanism and magnetism in carbothermal synthesized Fe3O4 nanoparticles from solution combustion precursors

    Science.gov (United States)

    Wang, Xuanli; Qin, Mingli; Cao, Zhiqin; Jia, Baorui; Gu, Yueru; Qu, Xuanhui; Volinsky, Alex A.

    2016-12-01

    Magnetic Fe3O4 nanoparticles were prepared by carbothermal reduction using solution combustion synthesis precursors derived from ferric nitrate (oxidizer), glycine (fuel) and glucose (carbon source) mixed solution. In this paper, the growth mechanism and magnetism in Fe3O4 nanoparticles were investigated by adjusting the glucose content in precursor and the heat temperature in carbothermal process. The products were analyzed by X-ray diffraction, Field emission scanning electron microscopy, Infrared adsorption method and Vibrating sample magnetometry. The results revealed that the more amount of glucose, the earlier Fe3O4 phase generated as temperature increasing. Depending on glucose content and thermal temperature, the average grain size of Fe3O4 nanoparticles varied from 19.9 nm to 48 nm and saturation magnetization changed from 21.2 emu/g to 71.77 emu/g, which indicated that the saturation magnetization of Fe3O4 nanoparticles fell off as the average grain size decreasing. These results were crucial not only from the application stand-point, but more importantly leaded to a new platform for further studies of high quality magnetic Fe3O4 particles at nanoscale.

  17. Superparamagnetic Au-Fe3O4 nanoparticles: one-pot synthesis, biofunctionalization and toxicity evaluation

    Science.gov (United States)

    Pariti, A.; Desai, P.; Maddirala, S. K. Y.; Ercal, N.; Katti, K. V.; Liang, X.; Nath, M.

    2014-09-01

    Superparamagnetic Au-Fe3O4 bifunctional nanoparticles have been synthesized using a single step hot-injection precipitation method. The synthesis involved using Fe(CO)5 as iron precursor and HAuCl4 as gold precursor in the presence of oleylamine and oleic acid. Oleylamine helps in reducing Au3+ to Au0 seeds which simultaneously oxidizes Fe(0) to form Au-Fe3O4 bifunctional nanoparticles. Triton® X-100 was employed as a highly viscous solvent to prevent agglomeration of Fe3O4 nanoparticles. Detailed characterization of these nanoparticles was performed by using x-ray powder diffraction, transmission electron microscopy, scanning tunneling electron microscopy, UV-visible spectroscopy, Mössbauer and magnetometry studies. To evaluate these nanoparticles’ applicability in biomedical applications, L-cysteine was attached to the Au-Fe3O4 nanoparticles and cytotoxicity of Au-Fe3O4 nanoparticles was tested using CHO cells by employing MTS assay. L-cysteine modified Au-Fe3O4 nanoparticles were qualitatively characterized using Fourier transform infrared spectroscopy and Raman spectroscopy; and quantitatively using acid ninhydrin assay. Investigations reveal that that this approach yields Au-Fe3O4 bifunctional nanoparticles with an average particle size of 80 nm. Mössbauer studies indicated the presence of Fe in Fe3+ in A and B sites (tetrahedral and octahedral, respectively) and Fe2+ in B sites (octahedral). Magnetic measurements also indicated that these nanoparticles were superparamagnetic in nature due to Fe3O4 region. The saturation magnetization for the bifunctional nanoparticles was observed to be ˜74 emu g-1, which is significantly higher than the previously reported Fe3O4 nanoparticles. Mössbauer studies indicated that there was no significant Fe(0) impurity that could be responsible for the superparamagnetic nature of these nanoparticles. None of the investigations showed any presence of other impurities such as Fe2O3 and FeOOH. These Au-Fe3O4 bifunctional

  18. A novel magneto-fluorescent microsphere: Preparation and characterization of polystyrene-supported Fe3O4 and CdS nanoparticles

    Science.gov (United States)

    Kaboudin, Babak; Ghaderian, Abolfazl

    2013-10-01

    Novel sulfonated polystyrene microsphere containing Fe3O4 and CdS nanoparticles have been prepared and characterized. A thorough structural characterization has been carried out by means of transmission electron microscopy (TEM), scanning electron microscopy (SEM) images, VSM data, EDS, and photoluminescence spectroscopy. The presence of the magnetic nanoparticles (Fe3O4) and CdS nanoparticles on the polystyrene microspheres has been demonstrated. Cadmium diethyl dithiophosphate (CDDP) has been used as a 3 in 1 precursor (cadmium, sulfur, and ligand source) for the synthesis of high-quality CdS nanoparticles on polystyrene microsphere containing Fe3O4 nanoparticles. This novel composite exhibits both fluorescence and magnetism properties that may be used in a novel bioprobe.

  19. Controllable synthesis and enhanced microwave absorbing properties of Fe3O4/NiFe2O4/Ni heterostructure porous rods

    Science.gov (United States)

    Li, Yana; Wu, Tong; Jin, Keying; Qian, Yao; Qian, Naxin; Jiang, Kedan; Wu, Wenhua; Tong, Guoxiu

    2016-11-01

    We developed a coordinated self-assembly/precipitate transfer/sintering method that allows the controllable synthesis of Fe3O4/NiFe2O4/Ni heterostructure porous rods (HPRs). A series of characterizations confirms that changing [Ni2+] can effectively control the crystal size, internal strain, composition, textural characteristics, and properties of HPRs. Molar percentages of Ni and NiFe2O4 in HPRs increase with [Ni2+] in various Boltzmann function modes. Saturation magnetization Ms and coercivity Hc show U-shaped change trends because of crystal size, composition, and interface magnetic coupling. High magnetic loss is maintained after decorating NiFe2O4 and Ni on the surface of Fe3O4 PRs. Controlling the NiFe2O4 interface layers and Ni content can improve impedance matching and dielectric losses, thereby leading to lighter weight, stronger absorption, and broader absorption band of Fe3O4/NiFe2O4/Ni HPRs than Fe3O4 PRs. An optimum EM wave absorbing property was exhibited by Fe3O4/NiFe2O4/Ni HPRs formed at [Ni2+] = 0.05 M. The maximum reflection loss (RL) reaches -58.4 dB at 13.68 GHz, which corresponds to a 2.1 mm matching thickness. The absorbing bandwidth (RL ≤ -20 dB) reaches 14.4 GHz with the sample thickness at 1.6-2.4 and 2.8-10.0 mm. These excellent properties verify that Fe3O4/NiFe2O4/Ni HPRs are promising candidates for new and effective absorptive materials.

  20. Magneto-optical and catalytic properties of Fe3O4@HA@Ag magnetic nanocomposite

    Science.gov (United States)

    Amir, Md.; Güner, S.; Yıldız, A.; Baykal, A.

    2017-01-01

    Fe3O4@HA@Ag magnetic nanocomposites (MNCs) were successfully synthesized by the simple reflux method for the removal of azo dyes from the industrial aqueous media. Fe3O4@HA@AgMNCs exhibited high catalytic activity to reduce MB within 20 min from the waste water. The obtained materials were characterized by the means of different techniques. Powder X-ray diffraction (XRD) analysis confirmed the single-phase of Fe3O4 spinel structure. SEM and TEM analysis indicated that Fe3O4@HA@AgMNCs were nanoparticles like structure with small agglomeration. TG result showed that the products contained 9% of HA. The characteristic peaks of HA at 1601 cm-1 and 1703 cm-1 was observed by the means of FT-IR spectra of Fe3O4@HA@AgMNCs. The hysteresis (σ-H) curves revealed Fe3O4@HA@Ag MNCs exhibit a typical superparamagnetic characteristic with a saturation magnetization of 59.11 emu/g and measured magnetic moment is 2.45 μB. The average magnetic particle dimension (Dmag) is 13.25 nm. In accordance, the average crystallite and particle dimensions were obtained as 11.50 nm and 13.10 nm from XRD and TEM measurements, respectively. Magnetocrystalline anisotropy was offered as uniaxial and calculated effective anisotropy constant (Keff) is 2.96×105 Erg/g. The blocking temperature was estimated as 522 K. The size-dependent saturation magnetization suggests the existence of a magnetically dead layer as 0.793 nm for Fe3O4@HA@Ag MNCs. The UV-vis diffuse reflectance spectroscopy (DRS) and Kubelka-Munk theory were applied to determine the optical properties of powder samples. The direct optical energy band gap (Eg) values were estimated from Tauc plots between 1.62 eV and 2.12 eV.

  1. One-pot synthesis of in-situ carbon-coated Fe3O4 as a long-life lithium-ion battery anode

    Science.gov (United States)

    Liu, Min; Jin, Hongyun; Uchaker, Evan; Xie, Zhiqiang; Wang, Ying; Cao, Guozhong; Hou, Shuen; Li, Jiangyu

    2017-04-01

    Fe3O4 has been regarded as a promising anode material for lithium-ion batteries (LIBs) due to its high theoretical capacity, low cost, and environmental friendliness. In this work, we present a one-pot reducing-composite-hydroxide-mediated (R-CHM) method to synthesize in situ carbon-coated Fe3O4 (Fe3O4@C) at 280 °C using Fe(NO3)3 · 9H2O and PEG800 as raw materials and NaOH/KOH as the medium. The as-prepared Fe3O4 octahedron has an average size of 100 nm in diameter, covered by a carbon layer with a thickness of 3 nm, as revealed by FESEM and HRTEM images. When used as anode materials in LIBs, Fe3O4@C exhibited an outstanding rate capability (1006, 918, 825, 737, 622, 455 and 317 mAh g‑1 at 0.1, 0.2, 0.5, 0.8, 1.0, 1.5 and 2.0 A g‑1). Moreover, it presented an excellent cycling stability, with a retained capacity of 261 mAh g‑1 after 800 cycles under an extremely high specific current density of 2.0 A g‑1. Such results indicate that Fe3O4@C can provide a new route into the development of long-life electrodes for future rechargeable LIBs. Importantly, the R-CHM developed in our work can be extended for the synthesis of other carbon-coated electrodes for LIBs and functional nanostructures for broader applications.

  2. Magnetic nanoparticles of Fe3O4 enhance docetaxel-induced prostate cancer cell death

    Directory of Open Access Journals (Sweden)

    Sato A

    2013-08-01

    Full Text Available Akiko Sato,1 Naoki Itcho,1 Hitoshi Ishiguro,2,3 Daiki Okamoto,1 Naohito Kobayashi,4 Kazuaki Kawai,5 Hiroshi Kasai,5 Daisuke Kurioka,1 Hiroji Uemura,2 Yoshinobu Kubota,2 Masatoshi Watanabe11Laboratory for Medical Engineering, Division of Materials Science and Chemical Engineering, Graduate School of Engineering, Yokohama National University, Yokohama, Japan; 2Department of Urology, Yokohama City University Graduate School of Medicine, Yokohama, Japan; 3Photocatalyst Group, Kanagawa Academy of Science and Technology, Kawasaki, Japan; 4Department of Molecular Pathology, Yokohama City University Graduate School of Medicine, Yokohama, Japan; 5Department of Environmental Oncology, Institute of Industrial Ecological Sciences, University of Occupational and Environmental Health, Kitakyushu, JapanAbstract: Docetaxel (DTX is one of the most important anticancer drugs; however, the severity of its adverse effects detracts from its practical use in the clinic. Magnetic nanoparticles of Fe3O4 (MgNPs-Fe3O4 can enhance the delivery and efficacy of anticancer drugs. We investigated the effects of MgNPs-Fe3O4 or DTX alone, and in combination with prostate cancer cell growth in vitro, as well as with the mechanism underlying the cytotoxic effects. MgNPs-Fe3O4 caused dose-dependent increases in reactive oxygen species levels in DU145, PC-3, and LNCaP cells; 8-hydroxydeoxyguanosine levels were also elevated. MgNPs-Fe3O4 alone reduced the viability of LNCaP and PC-3 cells; however, MgNPs-Fe3O4 enhanced the cytotoxic effect of a low dose of DTX in all three cell lines. MgNPs-Fe3O4 also augmented the percentage of DU145 cells undergoing apoptosis following treatment with low dose DTX. Expression of nuclear transcription factor κB in DU145 was not affected by MgNPs-Fe3O4 or DTX alone; however, combined treatment suppressed nuclear transcription factor κB expression. These findings offer the possibility that MgNPs-Fe3O4–low dose DTX combination therapy may be

  3. Impact of Ti Incorporation on Hydroxylation and Wetting of Fe3O4

    Energy Technology Data Exchange (ETDEWEB)

    Stoerzinger, Kelsey A.; Pearce, Carolyn I.; Droubay, Timothy C.; Shutthanandan, Vaithiyalingam; Shavorskiy, Andrey; Bluhm, Hendrik; Rosso, Kevin M.

    2017-08-18

    Understanding the interaction of water with compositionally tuned metal oxides is central to exploiting their unique catalytic and magnetic properties. However, processes such as hydroxylation, wetting, and resulting changes in electronic structure at ambient conditions are challenging to probe in situ. Here, we examine the hydroxylation and wetting of Fe(3-x)TixO4 epitaxial films directly using ambient pressure X-ray photoelectron spectroscopy under controlled relative humidity. Fe2+ formation promoted by Ti4+ substitution for Fe3+ increases with hydroxylation, commensurate with a decrease in the surface work function or change in the surface dipole. The incorporation of small amounts of Ti (x=0.25) as a bulk dopant dramatically impacts hydroxylation, in part due to surface segregation, leading to coverages closer to that of TiO2 than Fe3O4. However, the Fe(3-x)TixO4 compositional series shows a similar affinity for water physisorption, which begins at notably lower relative humidity than on TiO2. The findings suggest that relative humidity rather than surface hydroxyl density controls wettability. Studies of this kind directly relate to rational design of doped magnetite into more active catalysts for UV/Fenton degradation, the adsorption of contaminants, and the development of spin filters.

  4. Functionalized Magnetic Fe3O4-β-Cyclodextran Nanoparticles for Efficient Removal of Bilirubin.

    Science.gov (United States)

    Han, Lulu; Chu, Simin; Wei, Houliang; Ren, Jun; Xu, Li; Jia, Lingyun

    2016-06-01

    Bilirubin (BR), as a lipophilic toxin, can binds and deposits in various tissues, especially the brain tissue, leading to hepatic coma and even death. Magnetic nanoparticles adsorbent modified by β-cyclodextran (Fe3O4-β-CD) was developed to remove the BR from the plasma. Fe3O4-β-CD nanoparticles was prepared through Schiff base reaction between the polyethylenimine (PEI)-modified Fe3O4 and aldehyde-functionalized β-CD, and characterized by Fourier transform infrared (FTIR) spectra, X-ray diffraction (XRD), transmission electron microscopy (TEM), vibrating sample magnetometer (VSM) and dynamic light scattering (DLS). Under optimized conditions, the Fe3O4-β-CD adsorbent could adsorb 225.6 mg/g free BR in PBS and reach the adsorption equilibrium within 90 min mainly through hydrophobic interaction; Moreover, the adsorbent displayed better adsorption capability in a dialysis system for BSA-bound bilirubin, plasma bilirubin and total bile acid, and the removal rates of those were 66%, 31% and 41% respectively. Because of the advantages of fast separation and purification process, low preparation cost, good adsorption capability for plasma bilirubin, Fe3O4-β-CD may become an economical and promising absorbent of BR for clinical applications.

  5. Synthesis of talc/Fe3O4 magnetic nanocomposites using chemical co-precipitation method.

    Science.gov (United States)

    Kalantari, Katayoon; Bin Ahmad, Mansor; Shameli, Kamyar; Khandanlou, Roshanak

    2013-01-01

    The aim of this research was to synthesize and develop a new method for the preparation of iron oxide (Fe(3)O(4)) nanoparticles on talc layers using an environmentally friendly process. The Fe(3)O(4) magnetic nanoparticles were synthesized using the chemical co-precipitation method on the exterior surface layer of talc mineral as a solid substrate. Ferric chloride, ferrous chloride, and sodium hydroxide were used as the Fe(3)O(4) precursor and reducing agent in talc. The talc was suspended in deionized water, and then ferrous and ferric ions were added to this solution and stirred. After the absorption of ions on the exterior surface of talc layers, the ions were reduced with sodium hydroxide. The reaction was carried out under a nonoxidizing oxygen-free environment. There were not many changes in the interlamellar space limits (d-spacing = 0.94-0.93 nm); therefore, Fe(3)O(4) nanoparticles formed on the exterior surface of talc, with an average size of 1.95-2.59 nm in diameter. Nanoparticles were characterized using different methods, including powder X-ray diffraction, transmission electron microscopy, emission scanning electron microscopy, energy dispersive X-ray spectroscopy, and Fourier transform infrared spectroscopy. These talc/Fe(3)O(4) nanocomposites may have potential applications in the chemical and biological industries.

  6. Structural and magnetic properties of core-shell Au/Fe3O4 nanoparticles

    Science.gov (United States)

    León Félix, L.; Coaquira, J. A. H.; Martínez, M. A. R.; Goya, G. F.; Mantilla, J.; Sousa, M. H.; Valladares, L. De Los Santos; Barnes, C. H. W.; Morais, P. C.

    2017-02-01

    We present a systematic study of core-shell Au/Fe3O4 nanoparticles produced by thermal decomposition under mild conditions. The morphology and crystal structure of the nanoparticles revealed the presence of Au core of d = (6.9 ± 1.0) nm surrounded by Fe3O4 shell with a thickness of ~3.5 nm, epitaxially grown onto the Au core surface. The Au/Fe3O4 core-shell structure was demonstrated by high angle annular dark field scanning transmission electron microscopy analysis. The magnetite shell grown on top of the Au nanoparticle displayed a thermal blocking state at temperatures below TB = 59 K and a relaxed state well above TB. Remarkably, an exchange bias effect was observed when cooling down the samples below room temperature under an external magnetic field. Moreover, the exchange bias field (HEX) started to appear at T~40 K and its value increased by decreasing the temperature. This effect has been assigned to the interaction of spins located in the magnetically disordered regions (in the inner and outer surface of the Fe3O4 shell) and spins located in the ordered region of the Fe3O4 shell.

  7. Catalytic wet air oxidation of phenol over Co-doped Fe3O4 nanoparticles

    Science.gov (United States)

    Song, Xu Chun; Zheng, Yi Fan; Yin, Hao Yong

    2013-08-01

    The Fe3O4 nanoparticles doped with cobalt ions have been successfully synthesized by the co-precipitation process. The X-ray diffraction, inductively coupled plasma, scanning electron microscopy, and transmission electron microscopy were used to characterize the as-prepared nanoparticles. The results show that the phase structure of the nanoparticles is spinel structure of pure Fe3O4 with the particle size ranging from 40 to 50 nm. The Co-doping concentration can be controlled by changing the atomic ratio of the stock materials. The catalytic activity of the Co-doped Fe3O4 was further investigated by decomposing the phenol in liquid phase. The results show that cobalt ions doping can improve the catalytic efficiency of Fe3O4 nanoparticles in phenol degradation with catalytic reaction fitting the first-order kinetics. According to the estimated reaction rate of Co-doped Fe3O4 nanoparticles at different temperatures, the activation energy was calculated to be 45.63 kJ/mol.

  8. Synthesis and characterization of surface-modified Fe3O4 super-paramagnetic nanoparticles.

    Science.gov (United States)

    Zhang, Zhan-jie; Ma, Jia; Xu, Shuang-bing; Ren, Jing-hua; Qin, You; Huang, Jing; Yang, Kun-yu; Zhang, Zhi-ping; Wu, Gang

    2014-04-01

    Aqueous dispersion and stability of Fe3O4 nanoparticles remain an issue unresolved since aggregation of naked iron nanoparticles in water. In this study, we successfully synthesized different Fe3O4 super-paramagnetic nanoparticles which were modified by three kinds of materials [DSPE-MPEG2000, TiO2 and poly acrylic acid (PAA)] and further detected their characteristics. Transmission electron microscopy (TEM) clearly showed sizes and morphology of the four kinds of nanoparticles. X-ray diffraction (XRD) proved successfully coating of the three kinds of nanoparticles and their structures were maintained. Vibrating sample magnetometer (VSM) verified that their magnetic properties fitted for the super-paramagnetic function. More importantly, the particle size analysis indicated that Fe3O4@PAA had a better size distribution, biocompatibility, stability and dispersion than the other two kinds of nanoparticles. In addition, using CNE2 cells as a model, we found that all nanoparticles were nontoxic. Taken together, our data suggest that Fe3O4@PAA nanoaparticles are superior in the application of biomedical field among the four kinds of Fe3O4 nanoparticles in the future.

  9. Synthesis of mesoporous γ-AlOOH@Fe3O4 magnetic nanomicrospheres

    Institute of Scientific and Technical Information of China (English)

    Yuanyuan Zheng; Shengfu Ji; Hongfei Liu; Ming Li; Hao Yang

    2012-01-01

    Mesoporous γ-AlOOH@Fe3O4 magnetic nanomicrospheres were synthesized using superparamagnetic Fe3O4 nanoparticles as the core and aluminum isopropoxide (AIP) as the aluminum source.The obtained magnetic nanomicrospheres were characterized by X-ray powder diffraction (XRD),transmission electron microscopy (TEM),scanning electron microscopy (SEM),N2 adsorption-desorption and vibrating sample magnetometry (VSM).The effects of preparation parameters such as hydrolysis time of AIP,concentration of AIP and coating layer number on microspheres were investigated.The results indicated that the mesoporous γ-AlOOH@Fe3O4 magnetic nanomicrospheres consisted ofa mesoporous γ-AlOOH shell and a Fe3O4 magnetic core.The diameter of γ-AlOOH@Fe3O4 nanomicrospheres was about 200 nm,the thickness of mesoporous γ-AlOOH shell was about 5 nm and the average pore size was 3.8 nm.The thickness of the mesoporous γ-AlOOH shell could be controlled via layer-by-layer coating times.The formation mechanism of the mesoporous γ-AlOOH shell involved a "chemisorption-hydrolysis" process.

  10. Weaving a two-dimensional fishing net from titanoniobate nanosheets embedded with Fe3O4 nanocrystals for highly efficient capture and isotope labeling of phosphopeptides

    Science.gov (United States)

    Chen, Xueqin; Li, Siyuan; Zhang, Xiaoxia; Min, Qianhao; Zhu, Jun-Jie

    2015-03-01

    Qualitative and quantitative characterization of phosphopeptides by means of mass spectrometry (MS) is the main goal of MS-based phosphoproteomics, but suffers from their low abundance in the large haystack of various biological molecules. Herein, we introduce two-dimensional (2D) metal oxides to tackle this biological separation issue. A nanocomposite composed of titanoniobate nanosheets embedded with Fe3O4 nanocrystals (Fe3O4-TiNbNS) is constructed via a facile cation-exchange approach, and adopted for the capture and isotope labeling of phosphopeptides. In this nanoarchitecture, the 2D titanoniobate nanosheets offer enlarged surface area and a spacious microenvironment for capturing phosphopeptides, while the Fe3O4 nanocrystals not only incorporate a magnetic response into the composite but, more importantly, also disrupt the restacking process between the titanoniobate nanosheets and thus preserve a greater specific surface for binding phosphopeptides. Owing to the extended active surface, abundant Lewis acid sites and excellent magnetic controllability, Fe3O4-TiNbNS demonstrates superior sensitivity, selectivity and capacity over homogeneous bulk metal oxides, layered oxides, and even restacked nanosheets in phosphopeptide enrichment, and further allows in situ isotope labeling to quantify aberrantly-regulated phosphopeptides from sera of leukemia patients. This composite nanosheet greatly contributes to the MS analysis of phosphopeptides and gives inspiration in the pursuit of 2D structured materials for separation of other biological molecules of interests.Qualitative and quantitative characterization of phosphopeptides by means of mass spectrometry (MS) is the main goal of MS-based phosphoproteomics, but suffers from their low abundance in the large haystack of various biological molecules. Herein, we introduce two-dimensional (2D) metal oxides to tackle this biological separation issue. A nanocomposite composed of titanoniobate nanosheets embedded with Fe3

  11. Magnetic Fe3O4@C nanoparticles as adsorbents for removal of amoxicillin from aqueous solution.

    Science.gov (United States)

    Kakavandi, Babak; Esrafili, Ali; Mohseni-Bandpi, Anoushiravan; Jonidi Jafari, Ahmad; Rezaei Kalantary, Roshanak

    2014-01-01

    In the present study, powder activated carbon (PAC) combined with Fe(3)O(4) magnetite nanoparticles (MNPs) were used for the preparation of magnetic composites (MNPs-PAC), which was used as an adsorbent for amoxicillin (AMX) removal. The properties of magnetic activated carbon were characterized by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, Brunaeur, Emmett and Teller and vibrating sample magnetometer. The operational factors affecting adsorption such as pH, contact time, adsorbent dosage, initial AMX concentration and temperature were studied in detail. The high surface area and saturation magnetization for the synthesized adsorbent were found to be 671.2 m(2)/g and 6.94 emu/g, respectively. The equilibrium time of the adsorption process was 90 min. Studies of adsorption equilibrium and kinetic models revealed that the adsorption of AMX onto MNPs-PAC followed Freundlich and Langmuir isotherms and pseudo-second-order kinetic models. The calculated values of the thermodynamic parameters, such as ΔG°, ΔH° and ΔS° demonstrated that the AMX adsorption was endothermic and spontaneous in nature. It could be concluded that MNPs-PAC have a great potential for antibiotic removal from aquatic media.

  12. Enzyme encapsulation in magnetic chitosan-Fe3O4 microparticles.

    Science.gov (United States)

    Costa-Silva, Tales Alexandre; Marques, Polyana Samorano; Souza, Cláudia Regina Fernandes; Said, Suraia; Oliveira, Wanderley Pereira

    2015-01-01

    Two simple procedures for the preparation of magnetic chitosan enzyme microparticles have been investigated and used for the immobilisation of endophytic fungus Cercospora kikuchii lipase as model enzyme. In the first case, lipase was entrapped in Fe3O4-chitosan microparticles by cross-linking method, while in the second case magnetic immobilised derivatives were produced using spray drying. Immobilised enzymes showed high enzyme activity retention and stability during storage without significant loss of activity. Glutaraldehyde Fe3O4-chitosan powders presented a higher lipase activity retention and storage stability than the others preparations. However, the immobilised derivatives produced by cross-linking showed higher enzyme activity after reuse cycles. The results proved that the magnetic Fe3O4-chitosan microparticles are an effective support for the enzyme immobilisation since the immobilised lipase showed best properties than the free form.

  13. Preparation and mechanism of Fe3O4/Au core/shell super-paramagnetic microspheres

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    In the presence of Fe3O4 nano-particles, a new type of super-paramagnetic Fe3O4/Au microspheres with core/shell structures was prepared by reduction of Au3+ with hydroxylamine. The formation mechanism of the core/shell microspheres was studied in some detail. It was shown that the formation of the complex microspheres can be divided into two periods, that is, surface reaction-controlled process and diffusion-controlled process. The relative time lasted by either process depends upon the amount of Fe3O4 added and the initial concentration of Au3+. XPS analysis revealed that along with increasing in coating amount, the strength of the characteristic peaks of Au increased, and the Auger peaks of Fe weakened and even disappeared. Size distribution analysis showed that the core/shell microspheres are of an average diameter of 180 nm, a little bit larger than those before coating.

  14. Controlled Synthesis and Characterization of Monodisperse Fe3O4 Nanoparticles

    Institute of Scientific and Technical Information of China (English)

    SHI,Rongrong; GAO,Guanhua; YI,Ran; ZHOU,Kechao; QIU,Guanzhou; LIU,Xiaohe

    2009-01-01

    Monodisperse Fe3O4 nanoparticles were successfully synthesized through the thermal decomposition of iron acetylacetonate in octadecene solvent in the presence of oleic acid and oleylamine.The influences of experimental parameters,such as reacting temperature,amounts and kinds of surfactants,solvents,oleic acid and oleylamine,on the size and shape of monodisperse Fe3O4 nanoparticles were discussed.The phase structures,morphology,and size of the as-prepared products were investigated in detail by X-ray diffraction (XRD),transmission electron microscopy (TEM),selected area electron diffraction (SAED) and high-resolution transmission electron microscopy (HRTEM).Magnetic property was measured using a vibrating sample magnetometer (VSM) at room temperature,which revealed that Fe3O4 nanoparticles were of ferromagnetism with a saturation magnetization (Ms) of 74.0 emu/g and coercivity (Hc) of 72.6 Oe.

  15. Preparation of Fe3O4Spherical Nanoporous Particles Facilitated by Polyethylene Glycol 4000

    Directory of Open Access Journals (Sweden)

    Wang Li-Li

    2009-01-01

    Full Text Available Abstract Much interest has been attracted to the magnetic materials with porous structure because of their unique properties and potential applications. In this report, Fe3O4nanoporous particles assembled from small Fe3O4nanoparticles have been prepared by thermal decomposition of iron acetylacetonate in the presence of polyethylene glycol 4000. The size of the spherical nanoporous particles is 100–200 nm. Surface area measurement shows that these Fe3O4nanoporous particles have a high surface area of 87.5 m2/g. Magnetization measurement and Mössbauer spectrum indicate that these particles are nearly superparamagnetic at room temperature. It is found that the morphology of the products is greatly influenced by polyethylene glycol concentration and the polymerization degree of polyethylene glycol. Polyethylene glycol molecules are believed to facilitate the formation of the spherical assembly.

  16. Magnetic Control of Fe3O4 Nanomaterial for Fat Ablation in Microchannel

    Directory of Open Access Journals (Sweden)

    Ming Chang

    2015-11-01

    Full Text Available In this study, surface modification of iron (II, III oxide Fe3O4 nanoparticles by oleic acid (OA coating is investigated for the microablation of fat in a microchannel. The nanoparticles are synthesized by the co-precipitation method and then dispersed in organic solvent prior to mixing with the OA. The magnetization, agglomeration, and particle size distribution properties of the OA-coated Fe3O4 nanoparticles are characterized. The surface modification of the Fe3O4 nanoparticles reveals that upon injection into a microchannel, the lipophilicity of the OA coating influences the movement of the nanoparticles across an oil-phase barrier. The motion of the nanoparticles is controlled using an AC magnetic field to induce magnetic torque and a static gradient field to control linear translation. The fat microablation process in a microchannel is demonstrated using an oscillating driving field of less than 1200 Am−1.

  17. Tunable fluorescence enhancement based on bandgap-adjustable 3D Fe3O4 nanoparticles

    Science.gov (United States)

    Hu, Fei; Gao, Suning; Zhu, Lili; Liao, Fan; Yang, Lulu; Shao, Mingwang

    2016-06-01

    Great progress has been made in fluorescence-based detection utilizing solid state enhanced substrates in recent years. However, it is still difficult to achieve reliable substrates with tunable enhancement factors. The present work shows liquid fluorescence enhanced substrates consisting of suspensions of Fe3O4 nanoparticles (NPs), which can assemble 3D photonic crystal under the external magnetic field. The photonic bandgap induced by the equilibrium of attractive magnetic force and repulsive electrostatic force between adjacent Fe3O4 NPs is utilized to enhance fluorescence intensity of dye molecules (including R6G, RB, Cy5, DMTPS-DCV) in a reversible and controllable manner. The results show that a maximum of 12.3-fold fluorescence enhancement is realized in the 3D Fe3O4 NP substrates without the utilization of metal particles for PCs/DMTPS-DCV (1.0 × 10-7 M, water fraction (f w) = 90%).

  18. Synthesis of cytocompatible Fe3O4@ZSM-5 nanocomposite as magnetic resonance imaging contrast agent

    Science.gov (United States)

    Atashi, Zahra; Divband, Baharak; Keshtkar, Ahmad; Khatamian, Maasoumeh; Farahmand-Zahed, Farzane; Nazarlo, Ali Kiani; Gharehaghaji, Nahideh

    2017-09-01

    In this study, ZSM-5 nano zeolite was used as a support material for iron oxide nanoparticles and the potential ability of the nanocomposite for magnetic resonance imaging (MRI) contrast agent was investigated. The nanocomposite was synthesized by hydrothermal method and characterized using X-ray diffraction and scanning electron microscopy. MRI was carried out by use of a 1.5 Tesla clinical scanner. The T2 weighted images were prepared and the r2 relaxivity was calculated. The sizes of Fe3O4 nanoparticles and related nanocomposite were 13-24 nm and 80-150 nm, respectively. Results of MTT assay confirmed that the prepared nanocomposite is cytocompatible. The r2 relaxivity of the Fe3O4@ZSM-5 nanocomposite was 457.1 mM-1 s-1. This study suggests that the Fe3O4@ZSM-5 nanocomposite has potential to use as an MRI T2 contrast agent.

  19. Comparison of schemes for preparing magnetic Fe3O4 nanoparticles

    Institute of Scientific and Technical Information of China (English)

    Ruoyu Hong; Jianhua Li; Jian Wang; Hongzhong Li

    2007-01-01

    Magnetic Fe3O4 nanoparticles were prepared by means of coprecipitation using NH3·H2O in water and in alcohol, and using NaOH in water. A series of instruments such as SEM, TEM, HRTEM, FT-IR, XRD and VSM were used to characterize the properties of the magnetic nanoparticles.was the longest. The process using NaOH in water was the simplest and the reaction time was the shortest, but the particle characteristics were inferior to those of the other two methods. The mean size of magnetic Fe3O4 nanoparticles prepared by coprecipitation in alcohol was the smallest among the three, but the nanoparticles aggregated severely. The magnetic Fe3O4 nanoparticles were coated with oleic acid using saturated sodium coated successfully and thoroughly.

  20. Evaluation of the antibacterial activity of Ag/Fe3O4 nanocomposites synthesized using starch.

    Science.gov (United States)

    Ghaseminezhad, Seyedeh Masumeh; Shojaosadati, Seyed Abbas

    2016-06-25

    Ag/Fe3O4 nanocomposites were successfully synthesized by a facile and cost-effective method using starch. Starch acts as both a biocompatible capping agent for Fe3O4 nanoparticles and a reducing agent for the reduction of silver ions in an alkaline medium. Samples were characterized using several analytical techniques including field emission scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), atomic absorption spectroscopy (AAS), and Fourier-transform infrared (FT-IR) spectroscopy. The vibrating sample magnetometer revealed that the nanocomposites were superparamagnetic. The Ag/Fe3O4 nanocomposites demonstrated a high-antibacterial activity against Escherichia coli as evaluated by means of minimum inhibitory concentration. The characteristics and antibacterial activity of the nanocomposites were significantly influenced by the concentration of silver nitrate and pH.

  1. Size-Controlled Synthesis of Fe3O4 Magnetic Nanoparticles in the Layers of Montmorillonite

    Directory of Open Access Journals (Sweden)

    Katayoon Kalantari

    2014-01-01

    Full Text Available Iron oxide nanoparticles (Fe3O4-NPs were synthesized using chemical coprecipitation method. Fe3O4-NPs are located in interlamellar space and external surfaces of montmorillonite (MMT as a solid supported at room temperature. The size of magnetite nanoparticles could be controlled by varying the amount of NaOH as reducing agent in the medium. The interlamellar space changed from 1.24 nm to 2.85 nm and average diameter of Fe3O4 nanoparticles was from 12.88 nm to 8.24 nm. The synthesized nanoparticles were characterized using some instruments such as transmission electron microscopy, powder X-ray diffraction, energy dispersive X-ray spectroscopy, field emission scanning electron microscopy, vibrating sample magnetometer, and Fourier transform infrared spectroscopy.

  2. Conjugating folate on superparamagnetic Fe3O4@Au nanoparticles using click chemistry

    Science.gov (United States)

    Shen, Xiaofang; Ge, Zhaoqiang; Pang, Yuehong

    2015-02-01

    Gold-coated magnetic core@shell nanoparticles, which exhibit magneto-optical properties, not only enhance the chemical stability of core and biocompatibility of surface, but also provide a combination of multimodal imaging and therapeutics. The conjugation of these tiny nanoparticles with specific biomolecules allows researchers to target the desired location. In this paper, superparamagnetic Fe3O4@Au nanoparticles were synthesized and functionalized with the azide group on the surface by formation of self-assembled monolayers. Folate (FA) molecules, non-immunogenic target ligands for cancer cells, are conjugated with alkyne and then immobilized on the azide-terminated Fe3O4@Au nanoparticles through copper(I)-catalyzed azide-alkyne cycloaddition (click reaction). Myelogenous leukemia K562 cells were used as a folate receptor (FR) model, which can be targeted and extracted by magnetic field after interaction with the Fe3O4@Au-FA nanoparticles.

  3. Preparation of surface plasmon resonance biosensor based on magnetic core/shell Fe3O4/SiO2 and Fe3O4/Ag/SiO2 nanoparticles.

    Science.gov (United States)

    Wang, Liying; Sun, Ying; Wang, Jing; Wang, Jian; Yu, Aimin; Zhang, Hanqi; Song, Daqian

    2011-06-01

    In this paper, surface plasmon resonance biosensors based on magnetic core/shell Fe(3)O(4)/SiO(2) and Fe(3)O(4)/Ag/SiO(2) nanoparticles were developed for immunoassay. With Fe(3)O(4) and Fe(3)O(4)/Ag nanoparticles being used as seeding materials, Fe(3)O(4)/SiO(2) and Fe(3)O(4)/Ag/SiO(2) nanoparticles were formed by hydrolysis of tetraethyl orthosilicate. The aldehyde group functionalized magnetic nanoparticles provide organic functionality for bioconjugation. The products were characterized by scanning electronic microscopy (SEM), transmission electronic microscopy (TEM), FTIR and UV-vis absorption spectrometry. The magnetic nanoparticles possess the unique superparamagnetism property, exceptional optical properties and good compatibilities, and could be used as immobilization matrix for goat anti-rabbit IgG. The magnetic nanoparticles can be easily immobilized on the surface of SPR biosensor chip by a magnetic pillar. The effects of Fe(3)O(4)/SiO(2) and Fe(3)O(4)/Ag/SiO(2) nanoparticles on the sensitivity of SPR biosensors were also investigated. As a result, the SPR biosensors based on Fe(3)O(4)/SiO(2) nanoparticles and Fe(3)O(4)/Ag/SiO(2) nanoparticles exhibit a response for rabbit IgG in the concentration range of 1.25-20.00 μg ml(-1) and 0.30-20.00 μg ml(-1), respectively.

  4. Synthesis of talc/Fe3O4 magnetic nanocomposites using chemical co-precipitation method

    Directory of Open Access Journals (Sweden)

    Kalantari K

    2013-05-01

    Full Text Available Katayoon Kalantari,1 Mansor Bin Ahmad,1,* Kamyar Shameli,1,2,* Roshanak Khandanlou11Department of Chemistry, Universiti Putra Malaysia, Serdang, Malaysia; 2Nanotechnology and Advance Materials Department, Materials and Energy Research Center, Karaj, Alborz, Karaj, Iran*These authors contributed equally to this workAbstract: The aim of this research was to synthesize and develop a new method for the preparation of iron oxide (Fe3O4 nanoparticles on talc layers using an environmentally friendly process. The Fe3O4 magnetic nanoparticles were synthesized using the chemical co-precipitation method on the exterior surface layer of talc mineral as a solid substrate. Ferric chloride, ferrous chloride, and sodium hydroxide were used as the Fe3O4 precursor and reducing agent in talc. The talc was suspended in deionized water, and then ferrous and ferric ions were added to this solution and stirred. After the absorption of ions on the exterior surface of talc layers, the ions were reduced with sodium hydroxide. The reaction was carried out under a nonoxidizing oxygen-free environment. There were not many changes in the interlamellar space limits (d-spacing = 0.94–0.93 nm; therefore, Fe3O4 nanoparticles formed on the exterior surface of talc, with an average size of 1.95–2.59 nm in diameter. Nanoparticles were characterized using different methods, including powder X-ray diffraction, transmission electron microscopy, emission scanning electron microscopy, energy dispersive X-ray spectroscopy, and Fourier transform infrared spectroscopy. These talc/Fe3O4 nanocomposites may have potential applications in the chemical and biological industries.Keywords: nanocomposites, Fe3O4 nanoparticles, talc, powder X-ray diffraction, scanning electron microscopy

  5. Green synthesis and characterization of superparamagnetic Fe 3O 4 nanoparticles

    Science.gov (United States)

    Lu, Wensheng; Shen, Yuhua; Xie, Anjian; Zhang, Weiqiang

    2010-07-01

    In this paper, we have first demonstrated a facile and green synthetic approach for preparing superparamagnetic Fe 3O 4 nanoparticles using α- D-glucose as the reducing agent and gluconic acid (the oxidative product of glucose) as stabilizer and dispersant. The X-ray powder diffraction (XRD), X-ray photoelectron spectrometry (XPS), and selected area electron diffraction (SAED) results showed that the inverse spinel structure pure phase polycrystalline Fe 3O 4 was obtained. The scanning electron microscopy (SEM) and transmission electron microscopy (TEM) results exhibited that Fe 3O 4 nanoparticles were roughly spherical shape and its average size was about 12.5 nm. The high-resolution TEM (HRTEM) result proved that the nanoparticles were structurally uniform with a lattice fringe spacing about 0.25 nm, which corresponded well with the values of 0.253 nm of the (3 1 1) lattice plane of the inverse spinel Fe 3O 4 obtained from the JCPDS database. The superconducting quantum interference device (SQUID) results revealed that the blocking temperature ( Tb) was 190 K, and that the magnetic hysteresis loop at 300 K showed a saturation magnetization of 60.5 emu/g, and the absence of coercivity and remanence indicated that the as-synthesized Fe 3O 4 nanoparticles had superparamagnetic properties. Fourier transform infrared spectroscopy (FT-IR) spectrum displayed that the characteristic band of Fe-O at 569 cm -1 was indicative of Fe 3O 4. This method might provide a new, mild, green, and economical concept for the synthesis of other nanomaterials.

  6. Magnetic Fe3O4 nanoparticle catalyzed chemiluminescence for detection of nitric oxide in living cells.

    Science.gov (United States)

    Wang, Huiliang; Li, Mei; Wang, Bing; Wang, Meng; Kurash, Ibrahim; Zhang, Xiangzhi; Feng, Weiyue

    2016-08-01

    Direct and real-time measurement of nitric oxide (NO) in biological media is very difficult due to its transient nature. Fe3O4 nanoparticles (nanoFe3O4) because of their unique catalytic activities have attracted much attention as catalysts in a variety of organic and inorganic reactions. In this work, we have developed a magnetic Fe3O4 nanoparticle-based rapid-capture system for real-time detection of cellular NO. The basic principle is that the nanoFe3O4 can catalyze the decomposition of H2O2 in the system to generate superoxide anion (O2 (·-)) and the O2 (·-) can serve as an effective NO(·) trapping agent yielding peroxynitrite oxide anion, ONOO(-). Then the concentration of NO in cells can be facilely determined via peroxynitrite-induced luminol chemiluminescence. The linear range of the method is from 10(-4) to 10(-8) mol/L, and the detection of limit (3σ, n = 11) is as low as 3.16 × 10(-9) mol/L. By using this method, the NO concentration in 0.1 and 0.5 mg/L LPS-stimulated BV2 cells was measured as 4.9 and 11.3 μM, respectively. Surface measurements by synchrotron X-ray photoelectron spectroscopy (SRXPS) and scanning transmission X-ray microscopy (STXM) demonstrate the catalytic mechanism of the nanoFe3O4-based system is that the significantly excess Fe(II) exists on the surface of nanoFe3O4 and mediates the rapid heterogeneous electron transfer, thus presenting a new Fe2O3 phase on the surface.

  7. Improved Photocatalytic Performance of a Novel Fe3O4@SiO2/Bi2SiO5 Hierarchical Nanostructure with Magnetic Recoverability

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    Xinxin Zhang

    2015-01-01

    Full Text Available Magnetic Fe3O4@SiO2/Bi2SiO5 composites with a novel hierarchical nanostructure were synthesized by sol-gel and hydrothermal methods and were characterized by scanning electron microscopy (SEM, X-ray diffraction (XRD, Fourier transform infrared spectroscopy (FTIR, X-ray photoelectron spectroscopy (XPS, and UV-visible diffuse reflectance spectroscopy (UV-vis DRS. It was found that the introduction of Fe3O4@SiO2 could turn the morphology of Bi2SiO5 from close-grained slab to hollow hierarchical architecture with fabric-structure. The Fe3O4@SiO2/Bi2SiO5 composite showed enhanced photodegradation efficiency for the degradation of reactive brilliant red dye (X-3B in aqueous solution under simulated sunlight irradiation, as compared with that of commercial P25. In addition, the Fe3O4@SiO2/Bi2SiO5 composite exhibited good magnetic recoverability and excellent photocatalytic stability (no obvious activity loss after recycling tests.

  8. Surface Organic Modification of Magnetic Iron Oxide Black Particles%磁性 Fe3O4微粒表面有机改性

    Institute of Scientific and Technical Information of China (English)

    施卫贤; 杨俊; 王亭杰; 金涌

    2001-01-01

    The affinity between magnetic particles (Fe3O4) and monomer or its polymer is a key factor affecting the function of micro spheres in the preparation of encapsulated magnetic micro-spheres(EMMS).Silane coupling[KH 570,CH2C(CH3)C(O)OC3H6Si(OCH3)3] was used for the surface modification of fine magnetic particles with 0.2~ 0.3 μ m in size and tetrahedron in crystal form.Ethanol/water solution was used as modification medium for silane coupling.Fourier transform infrared spectrometer and X ray photoelectron spectra analysis show that the coupling bonds chemically on the particle surface,leading to the affinity improvement between magnetic particles and monomer or its polymer.The encapsulated magnetic microspheres synthesized by dispersion polymerization of styrene in the presence of modified Fe3O4 particles are significantly improved compared with that when unmodified Fe3O4 particles are used.%在分散聚合法制备复合磁性微球过程中 ,采用硅烷偶联剂 KH 570对磁性 Fe3O4微粒进行表面改性 .红外光谱 (FTIR)、光电子能谱 (XPS)分析结果表明 ,偶联剂与磁性微粒表面以化学键形式结合 .改性后 ,Fe3O4微粒与单体及其聚合物之间具有良好的亲和性 ,采用改性后的磁性微粒可以显著改善磁性微球的性能指标 .

  9. Radiolytic formation of Fe3O4 nanoparticles: influence of radiation dose on structure and magnetic properties.

    Directory of Open Access Journals (Sweden)

    Alam Abedini

    Full Text Available Colloidal Fe3O4 nanoparticles were synthesized using a gamma-radiolysis method in an aqueous solution containing iron chloride in presence of polyvinyl alcohol and isopropanol as colloidal stabilizer and hydroxyl radical scavenger, respectively. Gamma irradiation was carried out in a 60Co gamma source chamber at different absorbed doses. Increasing the radiation dose above a certain critical dose (100 kGy leads to particle agglomeration enhancement, and this can influence the structure and crystallinity, and consequently the magnetic properties of the resultant particles. The optimal condition for formation of Fe3O4 nanoparticles with a uniform and narrow size distribution occurred at a dose of 100 kGy, as confirmed by X-ray diffractometry and transmission electron microscopy. A vibrating sample magnetometry study showed that, when radiation dose increased, the saturation and remanence magnetization decreased, whereas the coercivity and the remanence ratio increased. This magnetic behavior results from variations in crystallinity, surface effects, and particle size effects, which are all dependent on the radiation dose. In addition, Fourier transform infrared spectroscopy was performed to investigate the nature of the bonds formed between the polymer chains and the metal surface at different radiation doses.

  10. Adsorption mechanism of magnetically separable Fe3O4/graphene oxide hybrids

    Science.gov (United States)

    Ouyang, Ke; Zhu, Chuanhe; Zhao, Ya; Wang, Leichao; Xie, Shan; Wang, Qun

    2015-11-01

    A reclaimable Fe3O4/graphene oxide (GO) magnetic hybrid was successfully synthesized via a facile one-pot polyol approach and employed as a recyclable adsorbent for Bisphenol A (BPA) in aqueous solutions. The maximum adsorption capacity (qm) of the Fe3O4/GO hybrid for BPA was 72.80 mg/g at 273 K. The kinetics of the adsorption process and the adsorption isotherm data were fitted using the Freundlich equation and a pseudo-second-order kinetic model. The results of the thermodynamic parameters ΔH°, ΔS° and ΔG° showed that the adsorption process was exothermic and spontaneous. Furthermore, the reusability of the samples was investigated, and the results indicated that the samples exhibited high stability. The magnetic characterization demonstrated that hybrids were superparamagnetic and could be recovered conveniently by magnetic separation. The strong π-π interaction was determined to be the predominant driving force behind the adsorption of BPA onto the Fe3O4/GO hybrid. Therefore, the Fe3O4/GO hybrid could be regarded as a potential adsorbent for wastewater treatment and purification processes.

  11. Mössbauer investigations of Fe and Fe3O4 magnetic nanoparticles for hyperthermia applications

    Science.gov (United States)

    Kamzin, A. S.

    2016-03-01

    Magnetic nanoparticles of magnetite Fe3O4 and Fe synthesized by physical vapor deposition with a fast highly effective method using a solar energy have been studied. Targets have been prepared from tablets pressed from Fe3O4 or Fe powders. Relationships between the structure of nanoparticles and their magnetic properties have been investigated in order to understand principles of the control of the parameters of magnetic nanoparticles. Mössbauer investigations have revealed that the nanoparticles synthesized from tablets of both pure iron and Fe3O4 consist of two phases: pure iron and iron oxides (γ-Fe2O3 and Fe3O4). The high iron oxidability suggests that the synthesized nanoparticles have a core/shell structure, where the core is pure iron and the shell is an oxidized iron layer. Magnetite nanoparticles synthesized at a pressure of 80 Torr have the best parameters for hyperthermia due to their core/shell structure and core-to-shell volume ratio.

  12. Removal of Lignin from aqueous solution using Fe3O4 Nanoparticles as an effective adsorbent

    Directory of Open Access Journals (Sweden)

    Harajyoti Mazumdar

    2015-06-01

    Full Text Available The study was carried out to find out the adsorption efficiency of lignin from paper mill waste water by using Fe3O4 magnetic nanoparticles. The physico-chemical analysis of paper mill effluent results high B.O.D value. Separations of lignin from black liquor were done by acid precipitation method and removal of lignin was done with nanoparticles. Synthesis of nanoparticles was done by co-precipitation method by mixing and stirring of FeCl3.6H2O and FeCl2.4H2O solution at 2:1 molar ratio. The nanoparticles were characterized by using U.V-Vis spectrophotometer and X-Ray Diffraction. U.V-Vis spectra show absorbance spectra at around 585 nm while XRD revealed around 10 nm sizes of Fe3O4 MNPs. The removal efficiency of lignin by Fe3O4 MNPs was investigated at different pH and contact time. Maximum adsorption of lignin onto the surface of Fe3O4 MNPs took place at pH 2.5 and 10 mins of contact time. Desorption of lignin by nanoparticles was studies by using different organic solvents.

  13. Magnetic anisotropies in epitaxial Fe3O4/GaAs(100) patterned structures

    NARCIS (Netherlands)

    Zhang, W.; Wong, P.K.J.; Zhang, D.; Yuan, S.J.; Huang, Z.S.; Zhai, Y.; Wu, J.; Xu, Y.B.

    2014-01-01

    Previous studies on epitaxial Fe3O4 rings in the context of spin-transfer torque effect have revealed complicated and undesirable domain structures, attributed to the intrinsic fourfold magnetocrystalline anisotropy in the ferrite. In this Letter, we report a viable solution to this problem, utilizi

  14. Lipase NS81006 immobilized on Fe3O4 magnetic nanoparticles for biodiesel production

    Directory of Open Access Journals (Sweden)

    Thangaraj Baskar

    2016-06-01

    Full Text Available Lipase-catalyzed biodiesel production is being the object of extensive research due to the demerits of chemical based catalytic system. Lipase immobilized on Fe3O4 magnetic nanoparticles has the integrated advantages of traditional immobilized lipase and free lipase for its rather fast reaction rate and easy separation. It has been demonstrated that free lipase NS81006 has potential in catalyzing the alcoholysis of renewable oils for biodiesel preparation. In this study, Fe3O4 magnetic nanoparticles functionalized with organosilane compounds like (3-aminopropyltriethyloxysilane (APTES and (3-mercaptopropyltrimethoxysilane MPTMS were used as carriers for lipase immobilization. Lipase NS81006 was covalently bound to the organosilane-functionalized magnetic nanoparticles by using glutaraldehyde cross-linking reagent. A biodiesel yield of 89% and 81% could be achieved by lipase immobilized on APTES-Fe3O4 and MPTMS-Fe3O4 magnetic nanoparticles respectively under optimized conditions of oil to methanol molar ratio 1:3 with three step addition of methanol, reaction temperature 45°C and reaction time duration 12 h. The lipases immobilized on magnetic nanoparticles could be recovered easily by external magnetic field for further use.

  15. Preparation and characterization of spindle-like Fe3O4 mesoporous nanoparticles

    Directory of Open Access Journals (Sweden)

    Zhang Shaofeng

    2011-01-01

    Full Text Available Abstract Magnetic spindle-like Fe3O4 mesoporous nanoparticles with a length of 200 nm and diameter of 60 nm were successfully synthesized by reducing the spindle-like α-Fe2O3 NPs which were prepared by forced hydrolysis method. The obtained samples were characterized by transmission electron microscopy, powder X-ray diffraction, attenuated total reflection fourier transform infrared spectroscopy, field emission scanning electron microscopy, vibrating sample magnetometer, and nitrogen adsorption-desorption analysis techniques. The results show that α-Fe2O3 phase transformed into Fe3O4 phase after annealing in hydrogen atmosphere at 350°C. The as-prepared spindle-like Fe3O4 mesoporous NPs possess high Brunauer-Emmett-Teller (BET surface area up to ca. 7.9 m2 g-1. In addition, the Fe3O4 NPs present higher saturation magnetization (85.2 emu g-1 and excellent magnetic response behaviors, which have great potential applications in magnetic separation technology.

  16. One-step hydrothermal synthesis of magnetic Fe3O4 nanoparticles immobilized on polyamide fabric

    Science.gov (United States)

    Zhang, Hui; Zhu, Guoqing

    2012-03-01

    A thin film of nanosized Fe3O4 particles prepared by hydrothermal method was immobilized on the surface of polyamide 6 fiber using ferric trichloride and ferrous chloride as the precursor, N,N-dimethyl formamide as the swelling agent and sodium dodecyl sulfate as the dispersant agent. The morphology, crystalline phase, thermal stability, magnetization properties and chemical structure of polyamide 6 fabric before and after treatments were characterized by means of scanning electron microscope (SEM), transmission electron microscope (TEM), X-ray diffraction (XRD), thermal gravimetric analysis (TGA), differential scanning calorimetry (DSC), vibrating sample magnetometer (VSM) and X-ray photoelectron spectroscopy (XPS) techniques. The tensile properties and abrasion resistance were also measured. It was found that the inverse cubic spinel phase of Fe3O4 nanoparticles with an average size 50 nm were synthesized, and synchronously grafted onto polyamide fiber surface. As compared with the original fabric, the onset decomposition temperature of the Fe3O4-coated fabric decreased slightly. The saturation magnetization was measured to be 3.8 emu/g at temperature of 300 K. The tensile properties were enhanced to some extent mainly due to the fabric shrinkage. The abrasion resistance of the Fe3O4-coated fabric behaved well.

  17. SYNTHESIS OF M–Nd DOPED Fe3O4 NANOPARTICLES (M = Co ...

    African Journals Online (AJOL)

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    series of Nd, Nd-Co, Nd-Ce, Nd-Cr, Nd-Ni doped Fe3O4 nanoparticles were ... good crystal structure, small particle size and high magnetic saturation. ... mmol) and salt of M (3.6×10-3 mmol) (salt of M: cobalt nitrate or chromium(III) nitrate or.

  18. Green synthesis of soya bean sprouts-mediated superparamagnetic Fe 3O 4 nanoparticles

    Science.gov (United States)

    Cai, Yan; Shen, Yuhua; Xie, Anjian; Li, Shikuo; Wang, Xiufang

    2010-10-01

    Superparamagnetic Fe 3O 4 nanoparticles were first synthesized via soya bean sprouts (SBS) templates under ambient temperature and normal atmosphere. The reaction process was simple, eco-friendly, and convenient to handle. The morphology and crystalline phase of the nanoparticles were determined from scanning electron microscopy (SEM), transmission electron microscopy (TEM), selected area electron diffraction (SAED), and X-ray diffraction (XRD) spectra. The effect of SBS template on the formation of Fe 3O 4 nanoparticles was investigated using X-ray photoemission spectroscopy (XPS) and Fourier-transform infrared spectroscopy (FT-IR). The results indicate that spherical Fe 3O 4 nanoparticles with an average diameter of 8 nm simultaneously formed on the epidermal surface and the interior stem wall of SBS. The SBS are responsible for size and morphology control during the whole formation of Fe 3O 4 nanoparticles. In addition, the superconducting quantum interference device (SQUID) results indicate the products are superparamagnetic at room temperature, with blocking temperature ( TB) of 150 K and saturation magnetization of 37.1 emu/g.

  19. Hydrothermal synthesis of graphene oxide/multiwalled carbon nanotube/Fe3O4 ternary nanocomposite for removal of Cu (II) and methylene blue

    Science.gov (United States)

    Long, Zhihang; Zhan, Yingqing; Li, Fei; Wan, Xinyi; He, Yi; Hou, Chunyan; Hu, Hai

    2017-09-01

    In this work, highly activated graphene oxide/multiwalled carbon nanotube/Fe3O4 ternary nanocomposite adsorbent was prepared from a simple hydrothermal route by using ferrous sulfate as precursor. For this purpose, the graphene oxide/multiwalled carbon nanotube architectures were formed through the π-π attractions between them, followed by attaching Fe3O4 nanoparticles onto their surface. The structure and composition of as-prepared ternary nanocomposite were characterized by XRD, FTIR, XPS, SEM, TEM, Raman, TGA, and BET. It was found that the resultant porous graphene oxide/multiwalled carbon nanotube/Fe3O4 ternary nanocomposite with large surface area could effectively prevent the π-π stacking interactions between graphene oxide nanosheets and greatly improve sorption sites on the surfaces. Thus, owing to the unique ternary nanocomposite architecture and synergistic effect among various components, as-prepared ternary nanocomposite exhibited high separation efficiency when they were used to remove the Cu (II) and methylene blue from aqueous solutions. Furthermore, the adsorption isotherms of ternary nanocomposite structures for Cu (II) and methylene blue removal fitted the Langmuir isotherm model. This work demonstrated that the graphene oxide/multiwalled carbon nanotube/Fe3O4 ternary nanocomposite was promising as an efficient adsorbent for heavy metal ions and organic dye removal from wastewater in low concentration.

  20. Bacteria-Affinity 3D Macroporous Graphene/MWCNTs/Fe3O4 Foams for High-Performance Microbial Fuel Cells.

    Science.gov (United States)

    Song, Rong-Bin; Zhao, Cui-E; Jiang, Li-Ping; Abdel-Halim, Essam Sayed; Zhang, Jian-Rong; Zhu, Jun-Jie

    2016-06-29

    Promoting the performance of microbial fuel cells (MFCs) relies heavily on the structure design and composition tailoring of electrode materials. In this work, three-dimensional (3D) macroporous graphene foams incorporated with intercalated spacer of multiwalled carbon nanotubes (MWCNTs) and bacterial anchor of Fe3O4 nanospheres (named as G/MWCNTs/Fe3O4 foams) were first synthesized and used as anodes for Shewanella-inoculated microbial fuel cells (MFCs). Thanks to the macroporous structure of 3D graphene foams, the expanded electrode surface by MWCNTs spacing, as well as the high affinity of Fe3O4 nanospheres toward Shewanella oneidensis MR-1, the anode exhibited high bacterial loading capability. In addition to spacing graphene nanosheets for accommodating bacterial cells, MWCNTs paved a smoother way for electron transport in the electrode substrate of MFCs. Meanwhile, the embedded bioaffinity Fe3O4 nanospheres capable of preserving the bacterial metabolic activity provided guarantee for the long-term durability of the MFCs. With these merits, the constructed MFC possessed significantly higher power output and stronger stability than that with conventional graphite rod anode.

  1. Preparation, characterization and photocatalytic activity of Fe2O3/ZnO and Fe3O4/ZnO

    Directory of Open Access Journals (Sweden)

    Patij Shah

    2014-03-01

    Full Text Available Composite Iron oxide-Zinc oxide (α-Fe2O3/ZnO and Fe3O4/ZnO was synthesized by two step method. In the first step, uniform α-Fe2O3 and Fe3O4 particles were prepared through a hydrolysis process of ferric chloride at 80°C. In the second step, the ZnO particles were included in the α-Fe2O3 and Fe3O4 particles by a zinc acetate [Zn(Ac2·2H2O] assisted hydrothermal method at low temperature (90 °C. X-ray Powder Diffraction (XRD, Scanning Electron microscopy (SEM, Energy-dispersive X-ray spectroscopy (EDAX was used to study its structural properties. The α-Fe2O3 and ZnO phases were identified by XRD, energy dispersive X-ray analysis (EDAX. The photoactivities of α-Fe2O3/ZnO and Fe3O4/ZnO nanoparticles under UV irradiation were quantified by the degradation of formaldehyde. The determination of magnetic property was also carried out by Gouy balance method.

  2. Synthesis, characterization and wound healing imitation of Fe3O4 magnetic nanoparticle grafted by natural products

    Science.gov (United States)

    Pala, Sravan Kumar

    This research focused on the study of the core-shelled magnetic nanomaterials derived from a colloidal chemistry. The goals are four-fold: (1) synthesis of Fe3O4MNMs using colloidal chemistry. The Fe 3O4 MNMs were then grafted with extracts derived from natural products, namely Olecraceavar italica (broccoli), Boletus edulis (mushroom)and Solanum lycopersicum (tomato);(2)characterization of natural products by chromatography and mass spectrometry;(3) characterization of MNMs to determine their crystallinity, morphological and elemental composition by the state-of-the-art instruments; and (4) biological evaluation using Gram-negative and Gram-positive bacteria. The approach provides advantages to precisely control the composition and homogeneity. The second advantage of the colloidal chemistry is its user friendliness and feasibility. Due to the nature of the natural products, the compatibility of MNM is anticipated to be enhanced.In this chapter, the nanomaterials will be discussed from four perspectives,§1.1 Nanotechnology (§1.1), §1.2 Synthesis of nanomaterials; §1.3 The natural product extract,; §1.4 Characterization of nanomaterials; and §1.5Biological application of nanomaterials.Fig. 1 summarized the overarching goals of this study.

  3. [Dechlorination degradation of 2,4-D by nanoscale Fe3O4].

    Science.gov (United States)

    Fang, Guo-Dong; Si, You-Bin

    2010-06-01

    Reductive transformation of 2,4-Dichlorophenoxyacetic acid (2,4-D) by nanoscale Fe3O4 was studied, and the effects of 2,4-D initial concentration, the dosage of nanoscale Fe3O4, pH and temperature on degradation rate of 2,4-D were investigated. The results showed that 48% 2,4-D with initial concentration of 10 mg/L was transformed within 48 h in the presence of 300 mg/L nanoscale Fe3O4. The degradation of 2,4-D was a reductive dechlorination process, and the concentration of chloride ion increased sharply with the degration of the 2,4-D. Disappearance of parent species and formation of reaction intermediates and products were analyzed by LC/MS. The transformation of 2,4-D followed a primary pathway of its complete reduction to phenol and a secondary pathway of sequential reductive hydrogenolysis to 2,4-dichlorophenol (2,4-DCP), 4-chlorophenol (4-CP) or 2-chlorophenol (2-CP) and phenol. The degradation equations of 2,4-D by nanoscale Fe3O4 conformed to pseudo-first-order kinetics, and the reaction rate constant (K) of 4-CP, 2,4-DCP and phenol were 0.0043 h(-1), 0.0026 h(-1) and 0.0032 h(-1), respectively. The degradation rate increased with an increase in initial concentration of 2,4-D from 0 mg/L to 10 mg/L, and increasing the dosage of nanoscale Fe3O4 from 0 mg/L to 300 mg/L. The pH of reaction solution significantly influenced reductive degradation of 2,4-D, and the optimum pH value was 3.0. Besides, high temperature could improve dechlorination rate of 2,4-D.

  4. [Degradation of norfloxacin by nano-Fe3O4/H2O2].

    Science.gov (United States)

    Zhang, Di; Wang, Yi-Xuan; Niu, Hong-Yun; Meng, Zhao-Fu

    2011-10-01

    The degradation of norfloxacin in aquatic environment was studied in the presence of Fe3O4 nanoparticles and H2O2. The effects of solution pH, temperature, dose of catalysts and concentration of H2O2 on norfloxacin degradation were surveyed. The degradation behaviors of different substrates by nano-Fe3O4/H2O2 were investigated and the reaction mechanism of norfloxacin was discussed. The results showed that the reaction was strongly pH-dependent and favored in acidic solution (pH = 3.5). The removal efficiency of norfloxacin was enhanced with the increase of temperature, catalysts dosage and H2O2 concentration. The degradation efficiency of norfloxacin by nano-Fe3O4/H2O2 was significantly higher than those of sulfathiazole, phenolic and aniline compounds. In the presence of 4.4 mmol x L(-1) of H2O2, 0.80 g x L(-1) of Fe3O4 and T = 303 K, norfloxacin was degraded completely in 5 min. The F element in norfloxacin molecule existed totally as F(-) in solution within 5 min, and the removal efficiency of total organic carbon was 57% in 1 h. In the ESR spectrum of nano-Fe3O4/H2O2 system, the characteristic peaks of BMPO-*OH adduct was detected, however, the intensity of the peaks was reduced to 5% with the addition of tert-butanol, a strong *OH scavenger, and the degradation efficiency of norfloxacin was correspondingly decreased to 10% in 1 h. These results indicated that *OH played an important role on norfloxacin degradation, and the reaction proceeded based on a heterogeneous Fenton-like system.

  5. Synthesis and characterization of magnetically recyclable Ag nanoparticles immobilized on Fe3O4@C nanospheres with catalytic activity

    Science.gov (United States)

    Li, Wei-hong; Yue, Xiu-ping; Guo, Chang-sheng; Lv, Jia-pei; Liu, Si-si; Zhang, Yuan; Xu, Jian

    2015-04-01

    A novel approach for the synthesis of Ag-loaded Fe3O4@C nanospheres (Ag-Fe3O4@C) was successfully developed. The catalysts possessed a carbon-coated magnetic core and grew active silver nanoparticles on the outer shell using hydrazine monohydrate as the AgNO3 reductant in ethanol. The morphology, inner structure, and magnetic properties of the as-prepared composites were studied with transmission electron microscopy (TEM), X-ray powder diffraction (XRD), fourier translation infrared spectroscopy (FT-IR), and vibrating sample magnetometer (VSM) techniques. Catalytic activity was investigated by degrading rhodamine B (RhB) in the designed experiment. The obtained products were monodispersed and bifunctional with high magnetization, as well as exhibited excellent catalytic activity toward organic dye with 98% of RhB conversion within 20 min in the presence of NaBH4. The product also exhibited convenient magnetic separability and maintained high catalytic activity after six cycle runs.

  6. Thiol-functionalized Fe3O4/SiO2 microspheres with superparamagnetism and their adsorption properties for Au(III) ion separation

    Science.gov (United States)

    Peng, Xiangqian; Zhang, Wei; Gai, Ligang; Jiang, Haihui; Tian, Yan

    2016-08-01

    Thiol-functionalized Fe3O4/SiO2 microspheres (Fe3O4/SiO2-SH) with high saturation magnetization (69.3 emu g-1), superparamagnetism, and good dispersibility have been prepared by an ethylene glycol reduction method in combination with a modified Stöber method. The as-prepared composite magnetic spheres are characterized with fourier transform infrared spectroscopy (FT-IR), zeta potential, X-ray powder diffraction (XRD), transmission electron microscopy (TEM), and superconducting quantum interference magnetometer, and tested in separation of Au(III) ions from aqueous solutions. The data for Au(III) adsorption on Fe3O4/SiO2-SH are analyzed with the Langmuir, Freundlich, Temkin, and Dubinin-Radushkevich isotherm models, and the pseudo-first-order, pseudo-second-order, and intraparticle diffusion kinetics models. The adsorption behaviors of Au(III) on Fe3O4/SiO2-SH follow the Langmuir isotherm model, and the adsorption process conforms to the pseudo-second-order kinetic model. The maximum adsorption capacity of Au(III) on Fe3O4/SiO2-SH is 43.7 mg g-1. Acetate anions play an important role yet Cu(II) ions have little interference in the adsorption of Au(III) on the adsorbent. A satisfactory recovery percentage of 89.5% is acquired by using an eluent with 1 M thiourea and 5% HCl, although thiols have a high affinity to Au(III) ions based on the hard-soft acid-base (HSAB) theory by Pearson.

  7. Fe3O4 nanoparticles for magnetic hyperthermia and drug delivery; synthesis, characterization and cellular studies

    Science.gov (United States)

    Palihawadana Arachchige, Maheshika

    In recent years, magnetic nanoparticles (MNPs), especially superparamagnetic Fe3O4nanoparticles, have attracted a great deal of attention because of their potential applications in biomedicine. Among the other applications, Magnetic hyperthermia (MHT), where localized heating is generated by means of relaxation processes in MNPs when subjected to a radio frequency magnetic field, has a great potential as a non-invasive cancer therapy treatment. Specific absorption rate (SAR), which measures the efficiency of heat generation, depends on magnetic properties of the particles such as saturation magnetization (M s), magnetic anisotropy (K), particle size distribution, magnetic dipolar interactions, and the rheological properties of the target medium.We have investigated MHT in two Fe3O4 ferrofluids prepared by co-precipitation (CP) and hydrothermal (HT) synthesis methods showing similar physical particle size distribution and Ms, but very different SAR 110 W/g and 40 W/g at room temperature. This observed reduction in SAR has been explained by taking the dipolar interactions into account using the so called T* model. Our analysis reveals that HT ferrofluid shows an order of magnitude higher effective dipolar interaction and a wider distribution of magnetic core size of MNPs compared to that of CP ferrofluid. We have studied dextran coated Gd-doped Fe3O4 nanoparticles as a potential candidate in theronostics for multimodal contrast imaging and cancer treatment by hyperthermia. The effect of surfactant on the MHT efficiency and cytotoxicity on human pancreatic cancer cells was explored as well. Though further in vivo study is necessary in the future, these results imply that the dextran coated Fe3O4 dispersion could maintain their high heating capacity in physiological environments while citric acid coating require further surface modification to reduce the non-specific protein adsorption. We have also investigated the traffic, distribution, and cytotoxicity, associated

  8. Seeded preparation of ultrathin FeS2 nanosheets from Fe3O4 nanoparticles

    Science.gov (United States)

    Li, Tingting; Liu, Huiwen; Wu, Zhennan; Liu, Yi; Guo, Zuoxing; Zhang, Hao

    2016-06-01

    FeS2 nanomaterials with two-dimensional features hold great promise for electrochemical and photovoltaic applications. However, the preparation of ultrathin FeS2 nanosheets is still challenging because of the lack of a tailor-made approach. In this work, FeS2 nanosheets with a thickness of 2.1 nm are prepared through a Fe3O4-seeded approach. Uniform Fe3O4 nanoparticles are foremost synthesized via the standard method in organic media. The injection of a S solution leads to the replacement of O in Fe3O4 through anion-exchange, which generates (110) facet-enriched FeS2 nuclei. The subsequent (110) facet-mediated oriented attachment and fusion of FeS2 nuclei produce ultrathin FeS2 nanosheets. As catalysts in the hydrogen evolution reaction, FeS2 nanosheets exhibit good electrochemical activity.FeS2 nanomaterials with two-dimensional features hold great promise for electrochemical and photovoltaic applications. However, the preparation of ultrathin FeS2 nanosheets is still challenging because of the lack of a tailor-made approach. In this work, FeS2 nanosheets with a thickness of 2.1 nm are prepared through a Fe3O4-seeded approach. Uniform Fe3O4 nanoparticles are foremost synthesized via the standard method in organic media. The injection of a S solution leads to the replacement of O in Fe3O4 through anion-exchange, which generates (110) facet-enriched FeS2 nuclei. The subsequent (110) facet-mediated oriented attachment and fusion of FeS2 nuclei produce ultrathin FeS2 nanosheets. As catalysts in the hydrogen evolution reaction, FeS2 nanosheets exhibit good electrochemical activity. Electronic supplementary information (ESI) available: EDX, AFM images, small-angle XRD pattern, SAED pattern, and TEM images of FeS2 nanosheets. See DOI: 10.1039/c6nr02211a

  9. Magnetic C-C@Fe3O4 double-shelled hollow microspheres via aerosol-based Fe3O4@C-SiO2 core-shell particles.

    Science.gov (United States)

    Zhu, Yangzhi; Li, Xiangcun; He, Gaohong; Qi, Xinhong

    2015-02-18

    Magnetic C-C@Fe3O4 hollow microspheres were prepared by using aerosol-based Fe3O4@C-SiO2 core-shell particles as templates. The magnetic double-shelled microspheres efficiently worked as carriers to load Pt nanoparticles, thus making the catalyst recyclable and reusable.

  10. Pickering-type ASA emulsions stabilized by Fe3O4 nanoparticles%纳米Fe3O4稳定的Pickering型ASA乳液

    Institute of Scientific and Technical Information of China (English)

    林兆云; 于得海; 李友明

    2014-01-01

    利用纳米Fe3O4作为稳定剂和乳化剂来制备Pickering型ASA(alkenyl succinic anhydride)施胶乳液,并研究了固体颗粒浓度、油水比、水分散相pH对乳液类型、稳定性、形态及施胶性能的影响。结果表明,纳米Fe3O4能够乳化制备均一稳定的Pickering型ASA乳液。乳液在室温下静置稳定,析出油相体积分数随固体颗粒用量的增加而增大,随油水比的增大而减小。油水比为2:1,水分散相浓度为0.1%(质量分数)时制备的ASA乳液稳定性最佳。固体颗粒部分吸附在油/水界面处,部分分散在分散相中,随分散相中固体颗粒浓度的增加,乳液稳定性变差。乳液静置分层之前,ASA发生部分水解。在放置1 h后用于纸页浆内施胶,随ASA乳液用量的增加,纸页表面接触角逐渐增大,且纸页表面粗糙度下降。在ASA的添加量为1.0%(质量分数)时,纸页表面接触角达到93.5°,纸页表面粗糙度为15.924μm。%Fe3O4 nanoparticles were used as stabilizer and emulsifier to prepare Pickering-type ASA (alkenyl succinic anhydride) emulsions, and the effects of particles concentration, volume ratio of oil/water and pH value on the type, stability, morphology and sizing performance of the emulsions were investigated. Fe3O4 nanoparticles were able to emulsify ASA to prepare homogeneous emulsions. When emulsions were placed without stirring at room temperature, the separated oil phase fraction increased with increasing particles concentration and decreased with increasing volume ratio of oil/water. Emulsions could keep homogeneous phase for 6 h as volume ratio of oil/water was 2 and particles concentration was 0.1%(mass). For stable emulsions, part of particles was absorbed at liquid-liquid interface and part of particles entered the dispersed phase, the stability of emulsions reduced with increasing particles concentration. Before the emulsions creamed, hydrolysis resistance was investigated

  11. Reversed ageing of Fe3O4 nanoparticles by hydrogen plasma

    Science.gov (United States)

    Schmitz-Antoniak, Carolin; Schmitz, Detlef; Warland, Anne; Svechkina, Nataliya; Salamon, Soma; Piamonteze, Cinthia; Wende, Heiko

    2016-02-01

    Magnetite (Fe3O4) nanoparticles suffer from severe ageing effects when exposed to air even when they are dispersed in a solvent limiting their applications. In this work, we show that this ageing can be fully reversed by a hydrogen plasma treatment. By x-ray absorption spectroscopy and its associated magnetic circular dichroism, the electronic structure and magnetic properties were studied before and after the plasma treatment and compared to results of freshly prepared magnetite nanoparticles. While aged magnetite nanoparticles exhibit a more γ-Fe2O3 like behaviour, the hydrogen plasma yields pure Fe3O4 nanoparticles. Monitoring the temperature dependence of the intra-atomic spin dipole contribution to the dichroic spectra gives evidence that the structural, electronic and magnetic properties of plasma treated magnetite nanoparticles can outperform the ones of the freshly prepared batch.

  12. Synthesis of Fe 3O 4 magnetic fluid used for magnetic resonance imaging and hyperthermia

    Science.gov (United States)

    Wang, Y. M.; Cao, X.; Liu, G. H.; Hong, R. Y.; Chen, Y. M.; Chen, X. F.; Li, H. Z.; Xu, B.; Wei, D. G.

    2011-12-01

    Fe3O4 magnetic nanoparticles were prepared by co-precipitation from FeSO4·7H2O and FeCl3·6H2O aqueous solutions using NaOH as precipitating reagent. The nanoparticles have an average size of 12 nm and exhibit superparamagnetism at room temperature. The nanoparticles were used to prepare a water-based magnetic fluid using oleic acid and Tween 80 as surfactants. The stability and magnetic properties of the magnetic fluid were characterized by Gouy magnetic balance. The experimental results imply that the hydrophilic block of Tween 80 can make the Fe3O4 nanoparticles suspending in water stable even after dilution and autoclaving. The magnetic fluid demonstrates excellent stability and fast magneto-temperature response, which can be used both in magnetic resonance imaging and magnetic fluid hyperthermia.

  13. Facile synthesis of pectin coated Fe3O4 nanospheres by the sonochemical method

    Science.gov (United States)

    Dai, Junjun; Wu, Shixi; Jiang, Wei; Li, Pingyun; Chen, Xiaolong; Liu, Li; Liu, Jie; Sun, Danping; Chen, Wei; Chen, Binhua; Li, Fengsheng

    2013-04-01

    Pectin coated Fe3O4 magnetic nanospheres (PCMNs) were synthesized by the sonochemical method. The Fe3O4 nanoparticles were prepared by chemical precipitation as reported in the previous articles, and the PCMNs were characterized by transmission electron microscopy, dynamic light scattering, thermogravimetric analysis, Fourier-transform infrared spectroscopy, a vibrating sample magnetometer and energy dispersive X-ray spectrum. The results indicated that the magnetic nanoparticles have been coated by pectin, magnetite content of which was up to 63%, with the saturation magnetization being 32.69 emu/g. The formation mechanism and further application of PCMNs have also been discussed. The results show that the PCMNs can be applied to biomedical applications.

  14. Facile synthesis of size tunable Fe3O4 nanoparticles in bisolvent system

    Science.gov (United States)

    Huang, Zhuanzhuan; Wu, Kelu; Yu, Qiao-He; Wang, Yi-Yan; Xing, Jiayi; Xia, Tian-Long

    2016-11-01

    Magnetic nanoparticle clusters with magnetization of about 80 emu/g and tunable size between 55 and 500 nm were synthesized through a bisolvent solvothermal process in the presence of ethylene glycol (EG) and diethylene glycol (DEG), triethylene glycol (TEG) or 1,2-propanediol (PG) with polyethylene glycol (PEG) or hexadecyltrimethyl ammonium bromide (CTAB) as surfactant. It was found that the volume ratio of EG to the other polyol played an important role in controlling the size and morphology of Fe3O4. Effect of the concentration of Ferric chloride hexahydrate (FeCl3·6H2O) and original reactants on controlling the size of Fe3O4 particles was also discussed.

  15. Synthesis and antibacterial properties of Fe3O4-Ag nanostructures

    Directory of Open Access Journals (Sweden)

    Pachla Anna

    2016-12-01

    Full Text Available Superparamagnetic iron oxide nanoparticles were obtained in the polyethylene glycol environment. An effect of precipitation and drying temperatures on the size of the prepared nanoparticles was observed. Superparamagnetic iron oxide Fe3O4, around of 15 nm, was obtained at a precipitation temperature of 80°C and a drying temperature of 60°C. The presence of functional groups characteristic for a polyethylene glycol surfactant on the surface of nanoparticles was confirmed by FTIR and XPS measurements. Silver nanoparticles were introduced by the impregnation. Fe3O4-Ag nanostructure with bactericidal properties against Escherichia coli species was produced. Interesting magnetic properties of these materials may be helpful to separate the bactericidal agent from the solution.

  16. Thermodynamics of Fe(II)Fe(III) oxide systems I. Hydrothermal Fe3O4

    Science.gov (United States)

    Bartel, J.J.; Westrum, E.F.; Haas, J.L.

    1976-01-01

    The heat capacity of a hydrothermally-prepared polycrystalline sample of Fe3O4 was measured from 53 to 350 K, primarily to study the thermophysics of the Verwey transitions. Although the bifurcation of the transition was confirmed, the sample was found to contain traces of manganese. The observed transition temperatures of 117.0 and 123.0 K are 3.7 and 4.2 K higher respectively than those found in pure Fe3O4. Ancillary analytical results are consistent and indicate a stoichiometry of Mn0.008Fe2.992O4 for this material. Characteristics in the transition region are ascribed to dopant effects. ?? 1976.

  17. Temperature-dependent anisotropic magnetoresistance inversion behaviors in Fe3O4 films

    Science.gov (United States)

    Yoon, Kap Soo; Hong, Jin Pyo

    2017-02-01

    We address the abnormal anisotropic magnetoresistance (AMR) reversal feature of half-metallic polycrystalline Fe3O4 films occurring at a specific temperature. Experimental results revealed a positive to negative MR transition in the Fe3O4 films at 264 K, which reflect the influence of additional domain wall scattering. These features was described by a correlation between domain wall resistance and inversion behavior of AMR with additional domain wall scattering factors. We further describe a possible model based on systematic structural and electrical measurements that employs a temperature-dependent domain wall width and spin diffusion length of the conducting electrons. This model allows for spin-flipping scattering of spin polarized electrons inside a proper domain width.

  18. Removal of Uranium (VI from aqueous solution by Uranium Benzamide Complex using AC_Fe3O4 Nanocomposite

    Directory of Open Access Journals (Sweden)

    Z Akbari Jonoush

    2014-07-01

    Conclusion: The removal of U(VI on AC_Fe3O4 nanocomposite with the aid of benzamide is a rapid and highly pH depended process. The maximum sorption capacity (15/87 mg/g of AC_Fe3O4 nanocomposite shows that this method is a suitable method for Uranium removal.

  19. Synthesis and characterization of graphene patterned with Fe3 O 4 nanoparticles

    Science.gov (United States)

    Chandra, Sayan; Stojak, K.; Ferizovic, D.; Munoz, M.; Phan, M. H.; Srikanth, H.

    2011-03-01

    Graphene has emerged as a very exciting material with its outstanding physical, chemical, and mechanical properties. Due to the presence of excess free electrons on a graphene surface, the possibility of graphene-mediated long-range interactions between magnetic nanoparticles would open up new avenues of research and device development. Our studies aimed to deposit ~ 9 nm Fe 3 O4 NPs on graphene layers to understand the role of the metallic interface in mediating the magnetic interactions between the particles. We successfully grew the high-quality graphene on Ni films using CVD and used the Langmuir-Blodgett technique to pattern different layers of the Fe 3 O4 nanoparticles on the graphene sheets. The samples were well structurally characterized by XRD, TEM, AFM, and Raman spectroscopy. Interestingly we have observed strong variation in the magnetic properties such as magnetic anisotropy of the NPs pattered graphene samples when compared to just the NPs. These results point to the important role of the metallic interface in mediating the magnetic interactions between the Fe 3 O4 nanoparticles.

  20. Synthesis and characterization of core-shell Fe3O4-gold-chitosan nanostructure

    Directory of Open Access Journals (Sweden)

    Salehizadeh Hossein

    2012-01-01

    Full Text Available Abstract Background Fe3O4-gold-chitosan core-shell nanostructure can be used in biotechnological and biomedical applications such as magnetic bioseparation, water and wastewater treatment, biodetection and bioimaging, drug delivery, and cancer treatment. Results Magnetite nanoparticles with an average size of 9.8 nm in diameter were synthesized using the chemical co-precipitation method. A gold-coated Fe3O4 monotonous core-shell nanostructure was produced with an average size of 15 nm in diameter by glucose reduction of Au3+ which is then stabilized with a chitosan cross linked by formaldehyde. The results of analyses with X-ray diffraction (XRD, Fourier Transformed Infrared Spectroscopy (FTIR, Transmission Electron Microscopy (TEM, and Atomic Force Microscopy (AFM indicated that the nanoparticles were regularly shaped, and agglomerate-free, with a narrow size distribution. Conclusions A rapid, mild method for synthesizing Fe3O4-gold nanoparticles using chitosan was investigated. A magnetic core-shell-chitosan nanocomposite, including both the supermagnetic properties of iron oxide and the optical characteristics of colloidal gold nanoparticles, was synthesized.

  1. Magnetic and electronic properties of Fe3O4/graphene heterostructures: First principles perspective

    KAUST Repository

    Mi, Wenbo

    2013-02-27

    Magnetic and electronic properties of Fe3O4(111)/graphene heterostructures are investigated by first principles calculations. Different structural models have been considered, which differ in the interface termination of Fe3O4(111) surface with respect to the same monolayer graphene. In three models, the magnetic moment of Fe(A) has a major change due to less O atoms surrounding Fe(A) atoms than Fe(B). Magnetic moment is enhanced by 8.5%, 18.5%, and 8.7% for models (a), (b), and (c), respectively. Furthermore, the spin polarization of models (a) and (c) is lowered due to the simultaneous occurrence of density of states of spin-up Fe(A) and spin-down Fe(B) at Fermi lever. The spin polarization of model (b) remains the same as that of bulk Fe3O4. Our results suggest that different interface terminations and Fe(A) play an important role in determining the magnetism strength and spin polarization.

  2. Synthesis and characterization of Fe3O4-SiO2-AgCl photocatalyst

    Science.gov (United States)

    Husni, H. N.; Mahmed, N.; Ngee, H. L.

    2016-07-01

    Magnetite-silica-silver chloride (Fe3O4-SiO2-AgCl) coreshell particles with AgCl crystallite size of 117 nm was prepared by a wet chemistry method at ambient temperature. The magnetite-core was synthesized by using iron (II) sulfate heptahydrate (FeSO4•7H2O) and iron (III) sulfate hydrate (Fe2(SO4)3) with ammonium hydroxide (NH4OH) as the precipitating agent. The silica-shell was synthesized by using a modified Stöber process. The silver ions (Ag+) was adsorbed onto the silica surface after Söber process, followed by the addition of Cl- and polyvinylpyrrolidone (PVP) for the formation of Fe3O4-SiO2-AgCl coreshell particles. The effectiveness of the synthesized photocatalyst was investigated by monitoring the degradation of the methylene blue (MB) under sunlight for five cycles. About 90 % of the MB solution can be degraded after 2 hours. The degradation of MB solution by the Fe3O4-SiO2-AgCl particles is highly efficient for first three cycles according to the MB concentration recorded by the UV-Visible spectroscopy (UV-Vis). Nevertheless, the synthesized particles could be a promising material for photocatalytic applications.

  3. Sustained magnetization oscillations in polyaniline-Fe3O4 nanocomposites

    Science.gov (United States)

    de Araújo, A. C. V.; Rodrigues, A. R.; de Azevedo, W. M.; Machado, F. L. A.; Rezende, S. M.

    2015-09-01

    We report experiments with polyaniline-Fe3O4 (PANI-Fe3O4) nanocomposites synthesized under several different conditions. With a reaction carried out at room temperature and assisted by intense ultra-violet (UV) irradiation, we observe sustained oscillations in the magnetization with a period of about 25 min. The oscillations are interpreted as the result of an oscillatory chemical reaction in which part of the Fe+2 ions of magnetite, Fe3O4, are oxidized by the UV irradiation to form Fe+3 so that a fraction of the magnetite content transforms into maghemite, γ-Fe2O3. Then, Fe+3 ions at the nanoparticle surfaces are reduced and transformed back into Fe+2, when acting as an oxidizing agent for polyaniline in the polymerization process. Since maghemite has smaller magnetization than magnetite, the oscillating chemical reaction results in the oscillatory magnetization. The observations are interpreted with the Lotka-Volterra nonlinear coupled equations with parameters that can be adjusted to fit very well the experimental data.

  4. Optical Properties of Fe3O4 Magnetic Fluid from Iron Sand

    Science.gov (United States)

    Puspitaningrum, A.; Taufiq, A.; Hidayat, A.; Sunaryono; Hidayat, N.; Samian

    2017-05-01

    Nowadays, a high sensitive sensor for the magnetic field has become an essential tool that vastly desired in several fields, especially in biomedical application. Therefore, the development of preparing material for the magnetic sensor becomes crucial to be conducted. In this experimnet, we propose the use of Fe3O4 magnetic fluid prepared from a local iron sand in Indonesia as a material for a magnetic sensor. In this work, optical activities of the Fe3O4 magnetic fluid as the effect of magneto-optics were performed under varying external magnetic field. The polarization direction change of the laser was detected as a function of the external magnetic field with the exponential function. Moreover, the intensity collected by a photodetector exhibited a linear correlation with the external magnetic field. These phenomena become strong evidence that the prepared Fe3O4 magnetic fluid opens potential to be applicated further as sensors, especially as a high sensitive optics-based sensor for the magnetic field.

  5. One-pot preparation of superparamagnetic attapulgite/Fe3O4/polydopamine nanocomposites for adsorption of methylene blue

    Science.gov (United States)

    Mu, Bin; Kang, Yuru; Zheng, Maosong; Wang, Aiqin

    2016-05-01

    Superparamagnetic attapulgite/Fe3O4/polydopamine nanocomposites have been facilely prepared by a one-pot process without the nitrogen protection, in which Fe(III) was served as both of the oxidant for dopamine and the precursor of Fe3O4 in the presence of attapulgite. The introduction of attapulgite can effectively induce the uniform encapsulation of polydopamine and Fe3O4 nanoparticles on the surface of attapulgite, preventing from the formation of the free aggregates of Fe3O4 nanoparticles. The as-prepared APT/Fe3O4/PANI nanocomposites can be used as an adsorbent for the removal of methylene blue, and the adsorption ratio toward 100 ppm of methylene blue could reach 95.8%.

  6. Synthesis, Characterizations of Superparamagnetic Fe3O4-Ag Hybrid Nanoparticles and Their Application for Highly Effective Bacteria Inactivation

    DEFF Research Database (Denmark)

    Tung, L.M.; Cong, N.X.; Huy, L.T.

    2016-01-01

    In recent years, outbreaks of infectious diseases caused by pathogenic micro-organisms pose a serious threat to public health. In this work, Fe3O4-Ag hybrid nanoparticles were synthesized by simple chemistry method and these prepared nanoparticles were used to investigate their antibacterial...... properties and mechanism against methicilline-resistant Staphylococcus aureus (MRSA) pathogen. The formation of dimer-like nanostructure of Fe3O4-Ag hybrid NPs was confirmed by X-ray diffraction and High-resolution Transmission Electron Microscopy. Our biological analysis revealed that the Fe3O4-Ag hybrid...... NPs showed more noticeable bactericidal activity than that of plain Fe3O4 NPs and Ag-NPs. We suggest that the enhancement in bactericidal activity of Fe3O4-Ag hybrid NPs might be likely from main factors such as: (i) enhanced surface area property of hybrid nanoparticles; (ii) the high catalytic...

  7. Aloe vera plant-extracted solution hydrothermal synthesis and magnetic properties of magnetite (Fe3O4) nanoparticles

    Science.gov (United States)

    Phumying, Santi; Labuayai, Sarawuth; Thomas, Chunpen; Amornkitbamrung, Vittaya; Swatsitang, Ekaphan; Maensiri, Santi

    2013-06-01

    Magnetite (Fe3O4) nanoparticles have been successfully synthesized by a novel hydrothermal method using ferric acetylacetonate (Fe(C5H8O2)3) and aloe vera plant-extracted solution. The influences of different reaction temperatures and times on the structure and magnetic properties of the synthesized Fe3O4 nanoparticles were investigated. The synthesized nanoparticles are crystalline and have particle sizes of ˜6-30 nm, as revealed by transmission electron microscopy (TEM). The results of X-ray diffraction (XRD), High resolution TEM (HRTEM) and selected area electron diffraction (SAED) indicate that the synthesized Fe3O4 nanoparticles have the inverse cubic spinel structure without the presence of any other phase impurities. The hysteresis loops of the Fe3O4 nanoparticles at room temperature show superparamagnetic behavior and the saturation magnetization of the Fe3O4 samples increases with increasing reaction temperature and time.

  8. Controlled synthesis and photocatalysis of sea urchin-like Fe3O4@TiO2@Ag nanocomposites

    Science.gov (United States)

    Zhao, Yilin; Tao, Chengran; Xiao, Gang; Wei, Guipeng; Li, Linghui; Liu, Changxia; Su, Haijia

    2016-02-01

    Based on the synergistic photocatalytic activities of nano-sized TiO2 and Ag, as well as the magnetic properties of Fe3O4, a sea urchin-like Fe3O4@TiO2@Ag nanocomposite (Fe3O4@TiO2@Ag NCs) is controllably synthesized with tunable cavity size, adjustable shell layer of TiO2 nanofiber, higher structural stability and larger specific surface area. Here, Fe3O4@TiO2@Ag NCs are obtained with Fe3O4 as the core and nanofiber TiO2/Fe3O4/Ag nanoheterojunctions as the shell; and Ag nanoparticles with diameter of approximately 4 nm are loaded both on TiO2 nanofibers and inside the cavities of sea urchin-like Fe3O4@TiO2 nanocomposites uniformly. Ag nanoparticles lead to the production of more photogenerated charges in the TiO2/Fe3O4/Ag heterojunction via LSPR absorption, and enhance the band-gap absorption of TiO2, while the Fe3O4 cocatalyst provides the active sites for oxygen reduction by the effective transfer of photogenerated electrons to oxygen. So the photocatalytic performance is improved due to the synergistic effect of TiO2/Fe3O4/Ag nanoheterojunctions. As photocatalysts under UV and visible irradiation, the as-synthesized nanocomposites display enhanced photocatalytic and recycling properties for the degradation of ampicillin. Moreover, they present better broad-spectrum antibiosis under visible irradiation. The enhanced photocatalytic activity and excellent chemical stability, in combination with the magnetic recyclability, makes this multifunctional nanostructure a promising candidate for antibiosis and remediation in aquatic environmental contamination in the future.Based on the synergistic photocatalytic activities of nano-sized TiO2 and Ag, as well as the magnetic properties of Fe3O4, a sea urchin-like Fe3O4@TiO2@Ag nanocomposite (Fe3O4@TiO2@Ag NCs) is controllably synthesized with tunable cavity size, adjustable shell layer of TiO2 nanofiber, higher structural stability and larger specific surface area. Here, Fe3O4@TiO2@Ag NCs are obtained with Fe3O4 as the

  9. Electrochemical behavior of Piroxicam on a glassy carbon electrode modified with nano-Fe3 O4-reduced graphene oxide and its electrochemical determination%吡罗昔康在纳米Fe3 O4-石墨烯复合修饰玻碳电极上的电化学行为及电分析研究

    Institute of Scientific and Technical Information of China (English)

    张青春; 张志华; 张瑞; 彭娟; 高作宁

    2015-01-01

    The nano-Fe3 O4 and reduced graphene oxide ( RGO ) composite modified glassy carbon electrode ( nano-Fe3 O4-RGO/GCE)was fabricated,the electrochemical behavior and electrochemical properties of the anti-inflammatory drug Piroxicam(PC)at the nano-Fe3 O4-RGO/GCE,RGO/GCE and GCE were investigated by electrochemical impedance spectroscopy( EIS) ,cyclic volta-mmetry(CV),square wave voltammetry(SWV),chronoamperometry(CA)and chronocoulometry(CC). The experimental results showed that the electrochemical response of PC is much greater on the nano-Fe3 O4-RGO/GCE than on the bare glassy carbon elec-trode. the oxidation peak currents increased linearly range from 2. 0×10-6 to 2. 0×10-4 mol·L-1 with the detection limit(S/N=3)of 5. 3×10-7 mol·L-1 and the recoverage is in the range of 100. 0% ~104. 0%. Compared with other modified electrode,the nano-Fe3 O4-graphene modified glassy carbon electrode was convenient to prepare,and it exhibited a satisfactory accuracy and precision, and long-term stability,and could be used in the determination of piroxicam in pharmaceutical.%采用纳米Fe3 O4粒子( nano-Fe3 O4)和石墨烯( Reduced Graphene Oxide,RGO)制备了nano-Fe3 O4-RGO复合材料修饰玻碳电极(nano-Fe3O4-RGO/GCE),采用循环伏安法(cyclic voltammetry,CV),方波伏安法(square wave voltammetry,SWV),计时电流法( chronoamperometry,CA),计时库仑法( chronocoulometry,CC)研究了吡罗昔康( Piroxicam,PC)在此复合修饰电极上的电化学行为及电化学动力学性质。实验结果表明,与GCE相比, nano-Fe3 O4-RGO/GCE对PC的电化学氧化作用有显著的促进作用,其氧化峰电流显著增加;对各种实验条件进行了优化,测得峰电流Ipa与PC浓度在2.0×10-6~2.0×10-4 mol·L-1范围内呈良好的线性关系,检出限(S/N=3)为5.3×10-7 mol·L-1,加标回收率为100.0%~104.0%。该方法快速,灵敏,并将nano-Fe3O4-RGO/GCE用于市售吡罗昔康片剂的测定,结果符合定量测定要求。

  10. Controlled synthesis and photocatalysis of sea urchin-like Fe3O4@TiO2@Ag nanocomposites.

    Science.gov (United States)

    Zhao, Yilin; Tao, Chengran; Xiao, Gang; Wei, Guipeng; Li, Linghui; Liu, Changxia; Su, Haijia

    2016-03-07

    Based on the synergistic photocatalytic activities of nano-sized TiO2 and Ag, as well as the magnetic properties of Fe3O4, a sea urchin-like Fe3O4@TiO2@Ag nanocomposite (Fe3O4@TiO2@Ag NCs) is controllably synthesized with tunable cavity size, adjustable shell layer of TiO2 nanofiber, higher structural stability and larger specific surface area. Here, Fe3O4@TiO2@Ag NCs are obtained with Fe3O4 as the core and nanofiber TiO2/Fe3O4/Ag nanoheterojunctions as the shell; and Ag nanoparticles with diameter of approximately 4 nm are loaded both on TiO2 nanofibers and inside the cavities of sea urchin-like Fe3O4@TiO2 nanocomposites uniformly. Ag nanoparticles lead to the production of more photogenerated charges in the TiO2/Fe3O4/Ag heterojunction via LSPR absorption, and enhance the band-gap absorption of TiO2, while the Fe3O4 cocatalyst provides the active sites for oxygen reduction by the effective transfer of photogenerated electrons to oxygen. So the photocatalytic performance is improved due to the synergistic effect of TiO2/Fe3O4/Ag nanoheterojunctions. As photocatalysts under UV and visible irradiation, the as-synthesized nanocomposites display enhanced photocatalytic and recycling properties for the degradation of ampicillin. Moreover, they present better broad-spectrum antibiosis under visible irradiation. The enhanced photocatalytic activity and excellent chemical stability, in combination with the magnetic recyclability, makes this multifunctional nanostructure a promising candidate for antibiosis and remediation in aquatic environmental contamination in the future.

  11. A comparative study on the morphology of P3HT:PCBM solar cells with the addition of Fe3O4 nanoparticles by spin and rod coating methods

    Science.gov (United States)

    Zhang, Wenluan; Nguyen, Ngoc A.; Murray, Roy; Xin, Jiyuan; Mackay, Michael E.

    2017-09-01

    Our previous study presented up to 20% power conversion efficiency (PCE) enhancement of poly(3-hexylthiophene):phenyl-C61-butyric acid methyl ester (P3HT:PCBM) solar cells under the Fe3O4 nanoparticles (NPs) self-assembly (SA) effect by spin coating. Fe3O4 NPs (about 11 nm hydrodynamic diameter) form a thin layer at the top interface of the light absorbing active layer, which results in the generation of PCBM rich region improving the charge transport (Zhang et al. Sol Energ Mat Sol C 160:126-133, 2017). In order to investigate the feasibility of this Fe3O4 NPs SA effect under large-scale production condition, a smooth rod was implemented to mimic roll-to-roll coating technique and yield active layers having about the same thickness as the spin-coated ones. Small angle neutron scattering and grazing incidence X-ray diffraction were employed finding out similar morphologies of the active layers by these two coating techniques. However, rod-coated solar cell's PCE decreases with the addition of Fe3O4 NPs compared with the one without them. This is because PCBM rich region is not created at the top interface of the active layer due to the absence of Fe3O4 NPs, which is attributed to the weak convective flow and low diffusion rate. Moreover, in the rod-coated solar cells, the presence of Fe3O4 NPs causes decrease in P3HT crystallinity, thus the charge transport and the device performance. Our study confirms the role of spin coating in the Fe3O4 NPs SA effect and enables researchers to explore this finding in other polymer nanocomposite systems.

  12. Preparation of Fe3O4 Magnetic Surface Imprinted Microspheres and the Ethyl Acetate Extract Flavonoids Raspberry Concentration of Active Ingredient Applied

    Directory of Open Access Journals (Sweden)

    Xie YiHui

    2016-01-01

    Full Text Available the study is used by the co-precipitation method to make some uniform particle size and have good Fe3O4 magnetic nanoparticles and their surface modified with oleic acid ; oleic acid as the carrier of Fe3O4, quercetin as template molecule, prepared by the microwave assisted molecular imprinted polymer magnetic nanospheres; In raspberry ethyl acetate extract fingerprints for the assessment index, with orthogonal design best preparation; Characterization of equilibrium adsorption constant Kd and maximum adsorption capacity Qmax by Scatchard model.The results show that: This study explores the preparation of MIPs polymerization time by ten times, prepared by the Fe3O4 nanometer level, greatly increase the MIPs of the specific surface area, thereby increase the amount of adsorption (Kd = 0.7322mg / L, Qmax = 18.92μmol / g. Successfully extract raspberry flavonoids active ingredients from ethyl acetate which can be used for rapid and large parts of ethyl acetate enrichment raspberry flavonoids.

  13. Effect of Fe(3)O(4) on the sedimentation and structure-property relationship of starch under different pHs.

    Science.gov (United States)

    Palanikumar, S; Siva, P; Meenarathi, B; Kannammal, L; Anbarasan, R

    2014-06-01

    The nanosized ferrite (Fe3O4) was synthesized and characterized by analytical techniques such as Fourier transform infrared (FTIR) spectroscopy, UV-visible spectroscopy, fluorescence spectroscopy and transmission electron microscopy (TEM). The structure-property relationship of starch was studied under three different pHs namely 3.8, 7.1 and 12.5. The starch treated under acidic condition was degraded. In a similar manner, the structure-property relationship of starch in the presence of ferrite nanoparticles at three different pHs, as mentioned above was studied. The starch/ferrite nanocomposite prepared under acidic condition showed a degraded structure. Further, the polymer/nanocomposite systems were characterized by analytical techniques such as FTIR, differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), vibrating sample measurement (VSM), TEM and scanning electron microscopy (SEM). Finally, the settling velocity of starch under three different pHs both in the presence and absence of Fe3O4 was carried out to ensure the role of pH and effect of Fe3O4 on the settling velocity of starch.

  14. Monodispersed Silica Nanospheres Encapsulating Fe3O4 and LaF3:Eu3+ Nanoparticles for MRI Contrast Agent and Luminescent Imaging

    Science.gov (United States)

    Tian, Yang; Yu, Binbin; Yang, Hong-Yu; Liao, Ji

    2013-03-01

    Bifunctional nanospheres of silica encapsulating Fe3O4 and LaF3:Eu nanoparticles were synthesized in a reverse microemulsion solution. The nanospheres were perfectly monodispersed with a small diameter of 20 nm. The composition of the bifunctional nanospheres was confirmed by powder X-ray diffraction. Their magnetic and luminescent properties were measured at room temperature. The relaxation efficiency and T2-weighted images showed the high-performance for the product as a resonance imaging contrast agent. In addition, a qualitative cell uptake in human cervical cancer HeLa cells demonstrated that the SFLE nanospheres were efficiently up-taken into cytosol. Taken together, these findings suggest that the SiO2/Fe3O4-LaF3:Eu3+ nanospheres are good luminescence probes for bio-imaging.

  15. Preparation of stable magnetic nanofluids containing Fe3O4@PPy nanoparticles by a novel one-pot route

    Directory of Open Access Journals (Sweden)

    Zhao Baobao

    2011-01-01

    Full Text Available Abstract Stable magnetic nanofluids containing Fe3O4@Polypyrrole (PPy nanoparticles (NPs were prepared by using a facile and novel method, in which one-pot route was used. FeCl3·6H2O was applied as the iron source, and the oxidizing agent to produce PPy. Trisodium citrate (Na3cit was used as the reducing reagent to form Fe3O4 NPs. The as-prepared nanofluid can keep long-term stability. The Fe3O4@PPy NPs can still keep dispersing well after the nanofluid has been standing for 1 month and no sedimentation is found. The polymerization reaction of the pyrrole monomers took place with Fe3+ ions as the initiator, in which these Fe3+ ions remained in the solution adsorbed on the surface of the Fe3O4 NPs. Thus, the core-shell NPs of Fe3O4@PPy were obtained. The particle size of the as-prepared Fe3O4@PPy can be easily controlled from 7 to 30 nm by the polymerization reaction of the pyrrole monomers. The steric stabilization and weight of the NPs affect the stability of the nanofluids. The as-prepared Fe3O4@PPy NPs exhibit superparamagnetic behavior.

  16. Physiological effects of magnetite (Fe3O4) nanoparticles on perennial ryegrass (Lolium perenne L.) and pumpkin (Cucurbita mixta) plants.

    Science.gov (United States)

    Wang, Huanhua; Kou, Xiaoming; Pei, Zhiguo; Xiao, John Q; Shan, Xiaoquan; Xing, Baoshan

    2011-03-01

    To date, knowledge gaps and associated uncertainties remain unaddressed on the effects of nanoparticles (NPs) on plants. This study was focused on revealing some of the physiological effects of magnetite (Fe(3)O(4)) NPs on perennial ryegrass (Lolium perenne L.) and pumpkin (Cucurbita mixta cv. white cushaw) plants under hydroponic conditions. This study for the first time reports that Fe(3)O(4) NPs often induced more oxidative stress than Fe(3)O(4) bulk particles in the ryegrass and pumpkin roots and shoots as indicated by significantly increased: (i) superoxide dismutase and catalase enzyme activities, and (ii) lipid peroxidation. However, tested Fe(3)O(4) NPs appear unable to be translocated in the ryegrass and pumpkin plants. This was supported by the following data: (i) No magnetization was detected in the shoots of either plant treated with 30, 100 and 500 mg l(-1) Fe(3)O(4) NPs; (ii) Fe K-edge X-ray absorption spectroscopic study confirmed that the coordination environment of Fe in these plant shoots was similar to that of Fe-citrate complexes, but not to that of Fe(3)O(4) NPs; and (iii) total Fe content in the ryegrass and pumpkin shoots treated with Fe(3)O(4) NPs was not significantly increased compared to that in the control shoots.

  17. Ultrasound-assisted removal of Acid Red 17 using nanosized Fe3O4-loaded coffee waste hydrochar.

    Science.gov (United States)

    Khataee, Alireza; Kayan, Berkant; Kalderis, Dimitrios; Karimi, Atefeh; Akay, Sema; Konsolakis, Michalis

    2017-03-01

    The Fe3O4-loaded coffee waste hydrochar (Fe3O4-CHC) was synthesized using a simple precipitation method. The as-prepared adsorbent was characterized using scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET) and Fourier transform infrared spectroscopy (FT-IR). The EDX analysis indicated the presence of Fe in the structure of Fe3O4-CHC. The specific surface area of hydrochar increased from 17.2 to 34.7m(2)/g after loading of Fe3O4 nanoparticles onto it. The prepared Fe3O4-CHC was used for removal of Acid Red 17 (AR17) through ultrasound-assisted process. The decolorization efficiency decreased from 100 to 74% with the increase in initial dye concentration and from 100 to 91 and 85% in the presence of NaCl and Na2SO4, respectively. The synthesized Fe3O4-CHC exhibited good stability in the repeated adsorption-desorption cycles. The high correlation coefficient (R(2)=0.997) obtained from Langmuir model indicated that physical and monolayer adsorption of dye molecules occurred on the Fe3O4-CHC surface. Furthermore, the by-products generated through the degradation of AR17 was identified by gas chromatography-mass spectrometry analysis. Copyright © 2016 Elsevier B.V. All rights reserved.

  18. Ferroic ordering and charge-spin-lattice order coupling in Gd doped Fe3O4 nanoparticles

    Science.gov (United States)

    Laha, Suvra; Abdelhamid, Ehab; Palihawadana Arachchige, Maheshika; Dixit, Ambesh; Lawes, Gavin; Naik, Vaman; Naik, Ratna

    Rare earth doped spinels have been extensively studied for their potential applications in magneto-optical recording and as MRI contrast agents. In the present study, we have investigated the effect of gadolinium doping (1-5 at.%) on the magnetic and dielectric properties of Fe3O4nanoparticles synthesized by the chemical co-precipitation method. The structure and morphology of the as-synthesized gadolinium doped Fe3O4(Gd-Fe3O4) nanoparticles were characterized by XRD, SEM and TEM, and the magnetic properties were measured by a Quantum Design physical property measurement system. We find that the penetration of excess Gd3+ ions into Fe3O4 spinel matrix significantly influences the average crystallite size and saturation magnetization in Gd-Fe3O4. The average crystallite size, estimated from XRD using Scherrer equation, increases with increasing Gd doping percentage and the saturation magnetization drops monotonically with excess Gd3+ ions. Interestingly, Gd- Fe3O4develops enhanced ferroelectric ordering at low temperatures. The details of the temperature dependent dielectric, ferroelectric and magnetocapacitance measurements to understand the onset of charge-spin-lattice coupling in Gd-Fe3O4 system will be presented.

  19. Modifying Fe3O4 microspheres with rhodamine hydrazide for selective detection and removal of Hg2+ ion in water.

    Science.gov (United States)

    Wang, Zhuqing; Wu, Dayu; Wu, Genhua; Yang, Ningning; Wu, Aiguo

    2013-01-15

    Rhodamine hydrazide modifying Fe(3)O(4) microspheres (Fe(3)O(4)-R6G) was developed for selective detection and removal of mercury ion from water. With a saturation magnetization of 74.2 emu/g, the Fe(3)O(4)-R6G could be simply recollected from water with magnetic separation within a few minutes. The selectivity and adsorption ability of Fe(3)O(4)-R6G for metal cations were studied by fluorophotometry and atomic absorption spectrometry, respectively. The results showed that Fe(3)O(4)-R6G exhibited excellent selectivity for sensing mercury ion over other metal ions in aqueous solution, and also adsorbed 91% of mercury ion. The maximum adsorption capacity of the Fe(3)O(4)-R6G for Hg(2+) ion was 37.4 μmol g(-1). The Fe(3)O(4)-R6G was successfully applied to the determination of Hg(2+) in environmental samples, and could be used repeatedly by treatment with tetrabutylammonium hydroxide. Copyright © 2012 Elsevier B.V. All rights reserved.

  20. 退火对Ag包裹Fe3O4@TiO2复合微球结构光催化剂性能影响%Influence of Annealing on the Micro-structure and Phocatalysts of Ag-Coated Fe3O4@TiO2 Microspheres

    Institute of Scientific and Technical Information of China (English)

    周祥博; 叶英杰; 刘忠良; 刘亲壮; 朱光平; 李兵; 代凯; 张永兴

    2015-01-01

    文章采用气热法制备Fe3O4@TiO2复合微纳米球结构光催化剂,对其在氩气气氛保护中进行450℃退火3 h;在退火后的Fe3O4@TiO2复合微纳米球结构表面包裹一层Ag纳米颗粒.利用X射线衍射仪(XRD)、场发射扫描电子显微镜(FESEM)、透射电子显微镜(TEM)、振动样品磁强计(VSM)和全自动微孔物理吸附和化学吸附分析仪(ASAP 2020 M+C)对Ag包裹退火后的Fe3O4@TiO2复合微球结构光催化剂进行微结构表征.以有机染料亚甲基蓝(MB)作为废水模型,研究Ag包裹退火后的Fe3O4@TiO2复合微纳米球的光催化性能.结果表明:Ag包裹退火后的Fe3O4@TiO2复合微纳米球结构光催化剂仍具有良好的磁性能,易回收重复利用,相对于退火后的Fe3O4@TiO2催化剂,其光催化活性显著提高.循环使用4次后,在1 h内,其对MB的降解率仍能达到91.8%.%The Fe3O4@TiO2 micro/nanospheres were prepared by the vapor–thermal method using TBOT as the titanium source,and then annealed in argon shield at 450 ℃ for 3h.Ag nanoparticles were coated on the surface of the Fe3O4@TiO2 microspheres annealed by photodeposition method.The micro/nano-structures were characterized by X-ray diffraction(XRD),filed-scanning electron microscope(FE-SEM),transmission elec⁃tron microscope (TEM),vibration sample magnetometer (VSM),and nitrogen adsorption and desorption iso⁃therms on a Micrometrics ASAP 2020 system.The photocatalytic activities were evaluated by photocatalytic degradation of Methylene blue (MB) as model reaction.The result shows that Ag-Coated Fe3O4@TiO2 an⁃nealed composite photocatalyst still has a good magnetic property.And they are also easy to recycle and reuse. Compared with the Fe3O4@TiO2 catalyst annealed,Ag-TiO2 heterogeneous composite microspheres exhibited enhanced photocatalytic activity in the decomposition of MB under ultraviolet light condition.This material al⁃so shows good catalytic stability

  1. Fabrication of Docetaxel Surfaced Fe3O4 Magnetite Nanoparticles and their Cytotoxicity on 4 T1 Breast Cancer Cells

    Directory of Open Access Journals (Sweden)

    MH Yazdi

    2012-08-01

    Full Text Available Background:In the recent years, there is an increasing attention to the using of Fe3O4 magnetite nanoparticles (MNPs as drug delivery systems. Application of this nanoparticles could profit advantages of nanomedicine to enhance biological activity of pharmaceutical ingredients. Methods:Fe3O4 MNPs were synthesised by a chemical method and characterized by transmission electron microscopy and energy-dispersive spectroscopy techniques. In the next step, docetaxel-coated Fe3O4 MNPs were prepared, using percipitation method. The surface chemistry of docetaxel-coated Fe3O4 MNPs as well as their thermal decomposition characteristics were examined using fourier transform infrared spectroscopy and thermogravimetric analyzer equipment, respectively. The cytotoxicity assay was conducted on 4 T1 breast cancer carsinoma by MTT assay to evaluate the possible in vitro antiproliferative effects of docetaxel-coated Fe3O4 MNPs. Results:During precipitation process, docetaxel molecules were precipitated on the surface of Fe3O4 MNPs by the ratio of 3:100 w/w which indicates that each milligram of coated Fe3O4 MNPs averagely contained 30 mug pure docetaxel compound. Docetaxel showed aniproliferative effects against mentioned cell line. The higestest concentartion of docetaxel (80 mug/ml caused about 80% cell death. However, the results demostarted that much lower amounts of docetaxel will be needed in combination of Fe3O4 MNPs to produce the potent antiproliferative effect compared to docetaxel alone. Dose response cytotoxicity assay of docetaxel-coated Fe3O4 MNPs against 4 T1 breast cancer cells showed that lower amount of docetaxel (0.6 mug/ml can exhibit higher cytotoxic effect against this cancer cell line (90% cell death.

  2. Fast removal of malachite green dye using novel superparamagnetic sodium alginate-coated Fe3O4 nanoparticles.

    Science.gov (United States)

    Mohammadi, Abbas; Daemi, Hamed; Barikani, Mehdi

    2014-08-01

    In this study, superparamagnetic sodium alginate-coated Fe3O4 nanoparticles (Alg-Fe3O4) as a novel magnetic adsorbent were prepared by in situ coprecipitation method, in which Fe3O4 nanoparticles were precipitated from FeCl3 and FeCl2 under alkaline medium in the presence of sodium alginate. The Alg-Fe3O4 nanoparticles were used for removal of malachite green (MG) from aqueous solutions using batch adsorption technique. The characterization of synthesized nanoparticles was performed using XRD, FTIR, TEM, TGA and vibrating sample magnetometer (VSM) techniques. FTIR analysis of synthesized nanoparticles provided the evidence that sodium alginate was successfully coated on the surface of Fe3O4 nanoparticles. The FT-IR and TGA characterization showed that the Alg-Fe3O4 nanoparticles contained about 14% (w/w) of sodium alginate. Moreover, TEM analysis indicated that the average diameter of the Alg-Fe3O4 nanoparticles was about 12nm. The effects of adsorbent dosage, pH and temperature were investigated on the adsorption properties of MG onto Alg-Fe3O4 nanoparticles. The equilibrium adsorption data were modeled using the Langmuir and Freundlich isotherms. The maximum adsorption capacity obtained from Langmuir isotherm equation was 47.84mg/g. The kinetics of adsorption of MG onto Alg-Fe3O4 nanoparticles were investigated using the pseudo-first-order and pseudo-second-order kinetic models. The results showed that the adsorption of MG onto nanoparticles followed pseudo-second-order kinetic model. Copyright © 2014 Elsevier B.V. All rights reserved.

  3. Gum arabic modified Fe3O4 nanoparticles cross linked with collagen for isolation of bacteria

    Directory of Open Access Journals (Sweden)

    Chittor Raghuraman

    2010-12-01

    Full Text Available Abstract Background Multifunctional magnetic nanoparticles are important class of materials in the field of nanobiotechnology, as it is an emerging area of research for material science and molecular biology researchers. One of the various methods to obtain multifunctional nanomaterials, molecular functionalization by attaching organic functional groups to nanomagnetic materials is an important technique. Recently, functionalized magnetic nanoparticles have been demonstrated to be useful in isolation/detection of dangerous pathogens (bacteria/viruses for human life. Iron (Fe based material especially FePt is used in the isolation of ultralow concentrations (2 cfu/ml of bacteria in less time and it has been demonstrated that van-FePt may be used as an alternative fast detection technique with respect to conventional polymerase chain reaction (PCR method. However, still further improved demonstrations are necessary with interest to biocompatibility and green chemistry. Herein, we report the synthesis of Fe3O4 nanoparticles by template medication and its application for the detection/isolation of S. aureus bacteria. Results The reduction of anhydrous Iron chloride (FeCl3 in presence of sodium borohydride and water soluble polyelectrolyte (polydiallyldimethyl ammonium chloride, PDADMAC produces black precipitates. The X-ray diffraction (XRD, XPS and TEM analysis of the precipitates dried at 373 K demonstrated the formation of nanocrystalline Fe3O4. Moreover, scanning electron microscopy (SEM showed isolated staphylococcous aureus (S. aureus bacteria at ultralow concentrations using collagen coated gum arabic modified iron oxide nanoparticles (CCGAMION. Conclusion We are able to synthesize nanocrystalline Fe3O4 and CCGAMION was able to isolate S. aureus bacteria at 8-10 cfu (colony forming units/ml within ~3 minutes.

  4. Use of aerosol route to fabricate positively charged Au/Fe3O4 Janus nanoparticles as multifunctional nanoplatforms

    Science.gov (United States)

    Byeon, Jeong Hoon; Park, Jae Hong

    2016-10-01

    Gold (Au)-decorated iron oxide (Fe3O4), Au/Fe3O4, Janus nanoparticles were fabricated via the continuous route for aerosol Au incorporation with Fe3O4 domains synthesized in an aqueous medium as multifunctional nanoplatforms. The fabricated nanoparticles were subsequently exposed to 185-nm UV light to generate positive charges on Au surfaces, and their activities were tested in computed tomography (CT) and magnetic resonance (MR) imaging, gene-delivery and photothermal therapy. No additional polymeric coatings of the Janus particles also had a unique ability to suppress inflammatory responses in macrophages challenged with lipopolysaccharide, which may be due to the absence of amine groups.

  5. Synthesis of water-dispersible poly-l-lysine-functionalized magnetic Fe3O4-(GO-MWCNTs) nanocomposite hybrid with a large surface area for high-efficiency removal of tartrazine and Pb(II).

    Science.gov (United States)

    Hu, Dan; Wan, Xiaodong; Li, Xiaohui; Liu, Jianguo; Zhou, Chunhua

    2017-03-07

    In this study, a novel, effective and environment-friendly methods was used to prepare poly-l-lysine (PLL)-functionalized magnetic Fe3O4-(GO-MWCNTs) hybrid composite with large surface area and abundant hydroxyl and amino groups. The as-prepared PLL-Fe3O4-(GO-MWCNTs) nanocomposite was systematically characterized by FT-IR, XRD, TGA, SEM, TEM, VSM and EDX. The PLL-Fe3O4-(GO-MWCNTs) hybrid composite exhibited excellent adsorption performance for the removal of a dye (tartrazine) and a heave metal (Pb(II)). The result showed that adsorption of Pb(II) reached equilibrium in 30min and adsorption of tartrazine reached equilibrium in approximately 60min. Most importantly, PLL-Fe3O4-(GO-MWCNTs) hybrid possesses high adsorption capacity, rapid separation, and less time-consuming. The equilibrium adsorption capacity was 1038.42mgg(-1) for Pb(II) and 775.19mgg(-1) for tartrazine under the optimal conditions. These two pollutants removal were found to obey Langmuir adsorption model, while the kinetics of adsorption followed pseudo-second-order kinetic model. A possible adsorption mechanism has been proposed where the chelation between PLL and Pb(II) or electrostatic interaction between GO and tartrazine. These results demonstrated the potential applications of PLL-Fe3O4-(GO-MWCNTs) hybrid composite in deep-purification of polluted water. Copyright © 2017 Elsevier B.V. All rights reserved.

  6. Tunneling Magneto-resistance in grain boundary tailored Fe3O4 nano structured thin films

    Science.gov (United States)

    Kumar, Ankit; Behera, Nilamani; Husain, Sajid; Chaudhary, Sujeet; Pandya, Dinesh K.

    2017-05-01

    The pulse DC sputtered nanostructured Fe3O4 thin films have been subjected to hydrocarbon treatment and vacuum annealing to investigate their effect on grain boundaries. Remarkably, this treatment causes a change in the crystallographic structure of the film from polycrystalline to (440) oriented one and enhancement in film conductivity. Hopping conduction mechanism changes to nearest-neighbor hoping above Verwey transition temperature of 110 K on treatment. Treatment also leads to grain boundary modification by incorporation of antiferro defects that inhibit an increase in MR despite enhanced electron conduction across grain boundaries. Our results follow the non-homogeneous grain boundary model.

  7. Passively Q-switched EDFL using Fe3O4-nanoparticle saturable absorber

    OpenAIRE

    Bai, Xuekun; Mou, Chengbo; Xu, Luxi; Huang, Sujuan; Wang, Tingyun; Pu, Shengli; Zeng, Xianglong

    2015-01-01

    We experimentally demonstrate a passively Q-switched erbium-doped fiber laser (EDFL) operation by using a saturable absorber based on Fe3O4 nanoparticles (FONP) in magnetic fluid (MF). As a kind of transition metal oxide, the FONP has a large nonlinear optical response with a fast response time for saturable absorber. By depositing MF at the end of optical fiber ferrule, we fabricated a FONP-based saturable absorber, which enables a strong light-matter interaction owing to the confined transm...

  8. Fe3O4(110)-(1 × 3) revisited: Periodic (111) nanofacets

    Science.gov (United States)

    Parkinson, Gareth S.; Lackner, Peter; Gamba, Oscar; Maaß, Sebastian; Gerhold, Stefan; Riva, Michele; Bliem, Roland; Diebold, Ulrike; Schmid, Michael

    2016-07-01

    The structure of the Fe3O4(110)-(1 × 3) surface was studied with scanning tunneling microscopy (STM), low-energy electron diffraction (LEED), and reflection high-energy electron diffraction (RHEED). The so-called one-dimensional reconstruction is characterized by bright rows that extend hundreds of nanometers in the [ 1 bar10] direction and have a periodicity of 2.52 nm in [001] in STM. It is concluded that this reconstruction is the result of a periodic faceting to expose {111}-type planes with a lower surface energy.

  9. A novel electrochemical DNA biosensor based on a modified magnetic bar carbon paste electrode with Fe3O4NPs-reduced graphene oxide/PANHS nanocomposite.

    Science.gov (United States)

    Jahanbani, Shahriar; Benvidi, Ali

    2016-11-01

    In this study, we have designed a label free DNA biosensor based on a magnetic bar carbon paste electrode (MBCPE) modified with nanomaterial of Fe3O4/reduced graphene oxide (Fe3O4NP-RGO) as a composite and 1- pyrenebutyric acid-N- hydroxysuccinimide ester (PANHS) as a linker for detection of DNA sequences. Probe (BRCA1 5382 insC mutation detection) strands were immobilized on the MBCPE/Fe3O4-RGO/PANHS electrode for the exact incubation time. The characterization of the modified electrode was studied using different techniques such as scanning electron microscopy (SEM), infrared spectroscopy (IR), vibrating sample magnetometer (VSM), electrochemical impedance spectroscopy (EIS) and cyclic voltammetry methods. Some experimental parameters such as immobilization time of probe DNA, time and temperature of hybridization process were investigated. Under the optimum conditions, the immobilization of the probe and its hybridization with the target DNA (Complementary DNA) were tested. This DNA biosensor revealed a good linear relationship between ∆Rct and logarithm of the complementary target DNA concentration ranging from 1.0×10(-18)molL(-1) to 1.0×10(-8)molL(-1) with a correlation coefficient of 0.9935 and a detection limit of 2.8×10(-19)molL(-1). In addition, the mentioned biosensor was satisfactorily applied for discriminating of complementary sequences from non-complementary sequences. The constructed biosensor (MBCPE/Fe3O4-RGO/PANHS/ssDNA) with high sensitivity, selectivity, stability, reproducibility and low cost can be used for detection of BRCA1 5382 insC mutation. Copyright © 2016 Elsevier B.V. All rights reserved.

  10. Antifungal activity of magnetically separable Fe3O4/ZnO/AgBr nanocomposites prepared by a facile microwave-assisted method

    Institute of Scientific and Technical Information of China (English)

    Abolghasem Hoseinzadeh; Aziz Habibi-Yangjeh; Mahdi Davari

    2016-01-01

    In the present work, magnetically separable Fe3O4/ZnO/AgBr nanocomposites with different weight ra-tios of Fe3O4 to ZnO/AgBr were prepared by a facile microwave-assisted method. The resultant samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission elec-tron microscopy (TEM), energy dispersive analysis of X-rays (EDX), and vibrating sample magnetometery (VSM). Antifungal activity of the as-prepared samples was evaluated against Fusarium graminearum and Fusarium oxysporum as two phytopathogenic fungi. Among the nanocomposites, the sample with 1:8 weight ratio of Fe3O4 to ZnO/AgBr was selected as the best nanocomposite. This nanocomposite in-activates Fusarium graminearum and Fusarium oxysporum at 120 and 60 min, respectively. Moreover, it was observed that the microwave irradiation time has considerable influence on the antifungal activity and the sample prepared by irradiation for 10 min showed the best activity. Moreover, the nano-composite without any thermal treatment displayed the superior activity.

  11. Facile synthesis of Fe3O4-graphene@mesoporous SiO2 nanocomposites for efficient removal of Methylene Blue

    Science.gov (United States)

    Wu, Xi-Lin; Shi, Yanpeng; Zhong, Shuxian; Lin, Hongjun; Chen, Jian-Rong

    2016-08-01

    Herein, we have developed a facile and low-cost method for the synthesis of novel graphene based nanosorbents. Firstly, well-defined Fe3O4 nanoparticles were decorated onto graphene sheets, and then a layer of mesoporous SiO2 were deposited on the surface of the Fe3O4-graphene composites. The obtained Fe3O4-graphene@mesoporous SiO2 nanocomposites (denoted as MG@m-SiO2) were characterized by scanning electron microscopic (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), Fourier transformed infrared (FTIR) spectroscopy and X-ray diffraction (XRD). The adsorptive property was investigated by using MG@m-SiO2 as sorbents and Methylene Blue (MB), a common dye, as model of the organic pollutants. Adsorption kinetics, isotherms, thermodynamics as well as effects of pH and adsorbent dose on the adsorption were studied. The adsorption isotherms and kinetics are better described by Langmuir isotherm model and pseudo-second-order kinetic model, respectively. Thermodynamic studies suggest that the adsorption of MB onto the MG@m-SiO2 is endothermic and spontaneous process. The results imply that the MG@m-SiO2 can be served as a cost-effective adsorbent for the removal of organic pollutants from aqueous solutions.

  12. A facile method for the preparation of bifunctional Mn:ZnS/ZnS/Fe3O4 magnetic and fluorescent nanocrystals

    Directory of Open Access Journals (Sweden)

    Houcine Labiadh

    2015-08-01

    Full Text Available Bifunctional magnetic and fluorescent core/shell/shell Mn:ZnS/ZnS/Fe3O4 nanocrystals were synthesized in a basic aqueous solution using 3-mercaptopropionic acid (MPA as a capping ligand. The structural and optical properties of the heterostructures were characterized by X-ray diffraction (XRD, dynamic light scattering (DLS, transmission electron microscopy (TEM, UV–vis spectroscopy and photoluminescence (PL spectroscopy. The PL spectra of Mn:ZnS/ZnS/Fe3O4 quantum dots (QDs showed marked visible emission around 584 nm related to the 4T1 → 6A1 Mn2+ transition. The PL quantum yield (QY and the remnant magnetization can be regulated by varying the thickness of the magnetic shell. The results showed that an increase in the thickness of the Fe3O4 magnetite layer around the Mn:ZnS/ZnS core reduced the PL QY but improved the magnetic properties of the composites. Nevertheless, a good compromise was achieved in order to maintain the dual modality of the nanocrystals, which may be promising candidates for various biological applications.

  13. Multifunctional nanocomposites Fe3O4@SiO2-EDTA for Pb(II) and Cu(II) removal from aqueous solutions

    Science.gov (United States)

    Liu, Yu; Fu, Ruiqi; Sun, Yue; Zhou, Xiaoxin; Baig, Shams Ali; Xu, Xinhua

    2016-04-01

    In this study, EDTA-functionalized Fe3O4 (Fe3O4@SiO2-EDTA) was prepared by silanization reaction between N-(trimethoxysilylpropyl) ethylenediamine triacetic acid (EDTA-silane) and hydroxyl groups for Pb(II) and Cu(II) removal from aqueous solutions. Fe3O4@SiO2-EDTA composites were characterized using SEM, TEM, EDX, FTIR, XPS, TGA and saturated magnetization techniques. Maximum Pb(II) adsorption capacity was found to be 114.94 mg g-1 with SiO2/EDTA molar ratio of 2.5:1. The adsorption rate was significantly fast and the equilibrium was reached within 10 min. The optimum pH was recorded to be 5.0. The maximum adsorption capacity of the studied heavy metal ions calculated by Langmuir model followed the order: Cu(II) (0.58 mmol g-1) > Pb(II) (0.55 mmol g-1) ≈ Ni(II) (0.55 mmol g-1) > Cd(II) (0.45 mmol g-1). Moreover, Pb(II) and Cu(II) adsorption capacities were not significantly affected by co-existing cations and NOM. These results suggested that this adsorbent can be considered as a promising adsorbent to remove Pb(II) and Cu(II) from wastewaters.

  14. Carbon-Coated Fe3O4/VOx Hollow Microboxes Derived from Metal-Organic Frameworks as a High-Performance Anode Material for Lithium-Ion Batteries.

    Science.gov (United States)

    Zhao, Zhi-Wei; Wen, Tao; Liang, Kuang; Jiang, Yi-Fan; Zhou, Xiao; Shen, Cong-Cong; Xu, An-Wu

    2017-02-01

    As the ever-growing demand for high-performance power sources, lithium-ion batteries with high storage capacities and outstanding rate performance have been widely considered as a promising storage device. In this work, starting with metal-organic frameworks, we have developed a facile approach to the synthesis of hybrid Fe3O4/VOx hollow microboxes via the process of hydrolysis and ion exchange and subsequent calcination. In the constructed architecture, the hollow structure provides an efficient lithium ion diffusion pathway and extra space to accommodate the volume expansion during the insertion and extraction of Li(+). With the assistance of carbon coating, the obtained Fe3O4/VOx@C microboxes exhibit excellent cyclability and enhanced rate performance when employed as an anode material for lithium-ion batteries. As a result, the obtained Fe3O4/VOx@C delivers a high Coulombic efficiency (near 100%) and outstanding reversible specific capacity of 742 mAh g(-1) after 400 cycles at a current density of 0.5 A g(-1). Moreover, a remarkable reversible capacity of 556 mAh g(-1) could be retained even at a current density of 2 A g(-1). This study provides a fundamental understanding for the rational design of other composite oxides as high-performance electrode materials for lithium-ion batteries.

  15. Fe3O4/salicylic acid nanoparticles versatility in magnetic mediated vascular nanoblockage

    Science.gov (United States)

    Mîndrilă, I.; Buteică, S. A.; Mihaiescu, D. E.; Badea, G.; Fudulu, A.; Mărgăritescu, D. N.

    2016-01-01

    An aqueous dispersion of Fe3O4/salicylic acid magnetic nanoparticles (SaMNPs) was synthesized by a modified Massart method, characterized by Inductively Coupled Plasma-Optic Emission Spectrometry (ICP-OES), High-Resolution Transmission Electron Microscopy (HRTEM) and Dynamic Light Scattering (DLS) methods, and tested on the chick chorioallantoic membrane (CAM) model to evaluate biocompatibility, biodistribution, intravascular time persistence, and ability to be magnetically target driven in order to block the blood supply into a tumor xenograft. ICP-OES, DLS, and HRTEM SaMNPs sample analyses showed a 0.356 mg/mL Fe concentration, a good stability in water (average Zeta potential of 39.3 mV), a hydrodynamic diameter around 52 nm and a core diameter in the 7-15 nm range for the Fe3O4 nanoparticles. In vivo CAM assay showed that SaMNPs were biocompatible with the chick embryo, were fixed almost completely by the liver, had no embolic potential, and a threshold-dose-dependent intravascular magnetic targeting time. Study on the CAM tumor model showed that SaMNPs could be used for long-term magnetically mediated nanoblocking of the capillary networks and 70-µm smaller arterioles.

  16. Fe3O4-based PLGA nanoparticles as MR contrast agents for the detection of thrombosis

    Science.gov (United States)

    Liu, Jia; Xu, Jie; Zhou, Jun; Zhang, Yu; Guo, Dajing; Wang, Zhigang

    2017-01-01

    Thrombotic disease is a great threat to human health, and early detection is particularly important. Magnetic resonance (MR) molecular imaging provides noninvasive imaging with the potential for early disease diagnosis. In this study, we developed Fe3O4-based poly(lactic-co-glycolic acid) (PLGA) nanoparticles (NPs) surface-modified with a cyclic Arg-Gly-Asp (cRGD) peptide as an MR contrast agent for the detection of thrombosis. The physical and chemical characteristics, biological toxicity, ability to target thrombi, and biodistribution of the NPs were studied. The Fe3O4-PLGA-cRGD NPs were constructed successfully, and hematologic and pathologic assays indicated no in vivo toxicity of the NPs. In a rat model of FeCl3-induced abdominal aorta thrombosis, the NPs readily and selectively accumulated on the surface of the thrombosis and under vascular endothelial cells ex vivo and in vivo. In the in vivo experiment, the biodistribution of the NPs suggested that the NPs might be internalized by the macrophages of the reticuloendothelial system in the liver and the spleen. The T2 signal decreased at the mural thrombus 10 min after injection and then gradually increased until 50 min. These results suggest that the NPs are suitable for in vivo molecular imaging of thrombosis under high shear stress conditions and represent a very promising MR contrast agent for sensitive and specific detection of thrombosis. PMID:28223802

  17. MAPLE Fabricated Fe3O4@Cinnamomum verum Antimicrobial Surfaces for Improved Gastrostomy Tubes

    Directory of Open Access Journals (Sweden)

    Alina Georgiana Anghel

    2014-06-01

    Full Text Available Cinnamomum verum-functionalized Fe3O4 nanoparticles of 9.4 nm in size were laser transferred by matrix assisted pulsed laser evaporation (MAPLE technique onto gastrostomy tubes (G-tubes for antibacterial activity evaluation toward Gram positive and Gram negative microbial colonization. X-ray diffraction analysis of the nanoparticle powder showed a polycrystalline magnetite structure, whereas infrared mapping confirmed the integrity of C. verum (CV functional groups after the laser transfer. The specific topography of the deposited films involved a uniform thin coating together with several aggregates of bio-functionalized magnetite particles covering the G-tubes. Cytotoxicity assays showed an increase of the G-tube surface biocompatibility after Fe3O4@CV treatment, allowing a normal development of endothelial cells up to five days of incubation. Microbiological assays on nanoparticle-modified G-tube surfaces have proved an improvement of anti-adherent properties, significantly reducing both Gram negative and Gram positive bacteria colonization.

  18. Magnetoelectric properties of epitaxial Fe3O4 thin films on (011) PMN-PT piezosubstrates

    Science.gov (United States)

    Tkach, Alexander; Baghaie Yazdi, Mehrdad; Foerster, Michael; Büttner, Felix; Vafaee, Mehran; Fries, Maximilian; Kläui, Mathias

    2015-01-01

    We determine the magnetic and magnetotransport properties of 33 nm thick Fe3O4 films epitaxially deposited by rf-magnetron sputtering on unpoled (011) [PbMg1/3Nb2/3O3] 0.68-[PbTiO3]0.32 (PMN-PT) substrates. The magnetoresistance (MR), as well as the magnetization reversal, strongly depend on the in-plane crystallographic direction of the epitaxial (011) Fe3O4 film and strain. When the magnetic field is applied along [100], the magnetization loops are slanted and the sign of the longitudinal MR changes from positive to negative around the Verwey transition at 125 K on cooling. Along the [01 1 ¯] direction, the loops are square shaped and the MR is negative above the switching field across the whole temperature range, just increasing in absolute value when cooling from 300 K to 150 K. The value of the MR is found to be strongly affected by poling the PMN-PT substrate, decreasing in the [100] direction and slightly increasing in the [01 1 ¯] direction upon poling, which results in a strained film.

  19. Magnetic Behaviour and Heating Effect of Fe3O4 Ferrofluids Composed of Monodisperse Nanoparticles

    Institute of Scientific and Technical Information of China (English)

    ZHANG Li-Ying; DOU Yong-Hua; ZHANG Ling; GU Hong-Chen

    2007-01-01

    Fe3O4 ferrofluids containing monodisperse Fe3O4 nanoparticles with different diameters of 8, 12, 16 and 18 nm are prepared by using high-temperature solution phase reaction. The particles have single crystal structures with narrow size distributions. At room temperature, the 8-nm ferrofluid shows superparamagnetic behaviour,whereas the others display hysteresis properties and the coercivity increases with the increasing particle size.The spin glass-like behaviour and cusps near 190K are observed on all ferrofluids according to the temperature variation of field-cooled (FC) and zero-field-cooled (ZFC) magnetization measurements. The cusps are found to be associated with the freezing point of the solvent. As a comparison, the ferrofluids are dried and the FC and ZFC magnetization curves of powdery samples are also investigated. It is found that the blocking temperatures for the powdery samples are higher than those for their corresponding ferrofluids. Moreover, the size dependent heating effect of the ferrofluids is also investigated in ac magnetic field with a frequency of 55 kHz and amplitude of 200 Oe.

  20. Controlling the Properties of Solvent-free Fe3O4 Nanofluids by Corona Structure

    Institute of Scientific and Technical Information of China (English)

    Yumo Tan; Yaping Zheng∗; Nan Wang; Aibo Zhang

    2012-01-01

    We studied the relationship between corona structure and properties of solvent-free Fe3O4 nanoflu-ids. We proposed a series of corona structures with different branched chains and synthesize different solvent-free nanofluids in order to show the effect of corona structure on the phase behavior, dispersion, as well as rheol-ogy properties. Results demonstrate novel liquid-like behaviors without solvent at room temperature. Fe3O4 magnetic nanoparticles content is bigger than 8%and its size is about 2∼3 nm. For the solvent-free nanofluids, the long chain corona has the internal plasticization, which can decrease the loss modulus of system, while the short chain of corona results in the high viscosity of nanofluids. Long alkyl chains of modifiers lead to lower viscosity and better flowability of nanofluids. The rheology and viscosity of the nanofluids are correlated to the microscopic structure of the corona, which provide an in-depth insight into the preparing nanofluids with promising applications based on their tunable and controllable physical properties.

  1. Highly regenerable carbon-Fe3O4 core-satellite nanospheres as oxygen reduction electrocatalyst and magnetic adsorbent

    Science.gov (United States)

    Zhou, Wenqiang; Liu, Minmin; Cai, Chao; Zhou, Haijun; Liu, Rui

    2017-02-01

    We present the synthesis and multifunctional utilization of core-satellite carbon-Fe3O4 nanoparticles to serve as the enabling platform for a range of applications including oxygen reduction reaction (ORR) and magnetic adsorbent. Starting from polydopamine (PDA) nanoparticles and Fe(NO3)3, carbon-Fe3O4 core-satellite nanospheres are synthesized through successive steps of impregnation, ammoniation and carbonization. The synergistic combination of Fe3O4 and N-doped carbon endows the nanocomposite with high electrochemical activity in ORR and mainly four electrons transferred in reaction process. Furthermore, carbon-Fe3O4 nanoparticles used as magnetic adsorbent exhibit the efficient removal of Rhodamine B from an aqueous solution. The recovery and reuse of the adsorbent is demonstrated 5 times without any detectible loss in activity.

  2. Sonocatalytic Methylene Blue in The Presence of Fe3O4-CuO-TiO2 Nanocomposites Heterostructure

    Science.gov (United States)

    Fauzian, Malleo; Jalaludin, Shofianina; Taufik, Ardiansyah; Saleh, Rosari

    2016-04-01

    In this work, the emphasis was mainly placed on investigating the sonocatalytic activity of Fe3O4-CuO-TiO2 nanocomposites heterostructure. The prepared samples were characterized by X-ray diffraction (XRD), Vibrating Sample Magnetometer (VSM), Brunauer-Emmett-Teller (BET) Surface Area Analysis. Methylene blue dye was selected to examine the sonocatalytic activity of Fe3O4-CuO-TiO2 nanocomposites heterostructure. The degradation reaction processes were monitored by UV-vis spectrophotometer. The influence on the activity of the Fe3O4-CuO-TiO2 nanocomposites heterostructure such as TiO2 loading was studied. The sonocatalyst Fe3O4-CuO-TiO2 with molar ratio of 1:1:5 showed the highest sonocatalytic activity. At last, the experiment also indicated that holes are the main reactive species in the photodegradation mechanism in methylene blue.

  3. The Preparation of Glucan-Fe3O4 Magnetic Nanoparticles and Its In Vivo Distribution in Mice

    Directory of Open Access Journals (Sweden)

    Fengdan Jin

    2014-01-01

    Full Text Available The glucan-Fe3O4 magnetic nanoparticles were prepared by hydrothermal method. The mixture of FeCl2 and glucan was stirred vigorously for half an hour under low temperature (15°C. KOH of 1 mol/L was dropwise added, slowly, into the solution until the pH to 12. Immediately, KNO3 was added and the temperature was raised to 75°C for an hour. All the processes of Fe3O4 crystal particles generation were under nitrogen. An atomic absorption spectrometry quantitative analysis method was built to determine the in vivo distribution of the glucan-Fe3O4 magnetic nanoparticles in mice. The diameter of glucan-Fe3O4 magnetic nanoparticles was about 25 nm and they were up taken by the liver primarily after intravenous administration via the tail.

  4. PREPARATION OF Fe3O4/PSt MAGNETIC PARTICLES IN THE PRESENCE OF MAGNETIC FLUID IN ETHANOL/WATER MIXTURE

    Institute of Scientific and Technical Information of China (English)

    Xiao-bin Ding; Zong-hua Sun; Guo-xiang Wan; Ying-yan Jiang

    1999-01-01

    Fe3O4/Polystyrene(PSt) magnetic particles with core/shell structure have been prepared in the presence of Fe3O4 magnetic fluid in ethanol/water medium by dispersion polymerization of styrene. A Fe3O4particle formation mechanism was proposed. According to this mechanism, the size of particle nuclei is determined by the extent of aggregation of Fe3O4/oligomer. Magnetic particles with diameter ranging from 5to 200μm were prepared under different reaction conditions. Some polymerization parameters such as the concentration of monomer, stabilizer, initiator, and ethanol which affect particle size and size distribution are discussed and their effect on particle formation are explained by the proposed mechanism.

  5. Effect of Fe3O4 Magnetic Nanoparticle Concentration on the Signal of Surface Plasmon Resonance (SPR) Spectroscopy

    Science.gov (United States)

    Oktivina, M.; Nurrohman, D. T.; Rinto, A. N. Q. Z.; Suharyadi, E.; Abraha, K.

    2017-05-01

    Effect of Fe3O4 magnetic nanoparticle concentration on the signal of surface plasmon resonance (SPR) spectra has been successfully observed. The Fe3O4 nanoparticles with a particle size of about 10.5 ± 0.2 nm were used as active materials to increase the SPR response. X-ray diffraction (XRD) pattern showed that Fe3O4 nanoparticles have a high degree of crystallinity with spinel structure. The SPR system was successfully set up by using a glass prism coupler in a Kretschmann configuration in which gold (Au) thin film was thermally evaporated on the prism base. A green laser of wavelength 543 nm was used as light source. The angular scan in the attenuated total reflection (ATR) spectra showed a dropping intensity. Those things clearly indicated the appearance of SPR coupling phenomenon on the interface of Au thin film. The SPR spectra of fixed Au masses were also performed with same angular positions of dips. The Fe3O4 nanoparticles were deposited on gold thin film as a third layer which was synthesized via co-precipitation method. Hence, it was observed that the variation of Fe3O4 concentration affected the SPR spectra profile. The concentrations of Fe3O4 nanoparticles are 1, 3, 5, 7, 9, and 11 mg/ml which correspond to the angle shift of 0.1°, 0.3°, 0.5°, 0.7°, 0.9°, and 1.0°, respectively. The SPR angle of the dip was shifted to higher value due to change of refractive index of the medium as Fe3O4 nanoparticles concentration increases. Based on this result, we can conclude that the angle shift of SPR increases with increasing concentration of Fe3O4 nanoparticles.

  6. Colorimetric aptasensing of ochratoxin A using Au@Fe3O4 nanoparticles as signal indicator and magnetic separator.

    Science.gov (United States)

    Wang, Chengquan; Qian, Jing; Wang, Kun; Yang, Xingwang; Liu, Qian; Hao, Nan; Wang, Chengke; Dong, Xiaoya; Huang, Xingyi

    2016-03-15

    Gold nanoparticles (Au NPs) doped Fe3O4 (Au@Fe3O4) NPs have been synthesized by a facile one-step solvothermal method. The peroxidase-like activity of Au@Fe3O4 NPs was effectively enhanced due to the synergistic effect between the Fe3O4 NPs and Au NPs. On this basis, an efficient colorimetric aptasensor has been developed using the intrinsic dual functionality of the Au@Fe3O4 NPs as signal indicator and magnetic separator. Initially, the amino-modified aptamer specific for a typical mycotoxin, ochratoxin A (OTA), was surface confined on the amino-terminated glass beads surafce using glutaraldehyde as a linker. Subsequently, the amino-modified capture DNA (cDNA) was labeled with the amino-functionalized Au@Fe3O4 NPs and the aptasensor was thus fabricated through the hybridization reaction between cDNA and the aptamers. While upon OTA addition, aptamers preferred to form the OTA-aptamer complex and the Au@Fe3O4 NPs linked on the cDNA were released into the bulk solution. Through a simple magnetic separation, the collected Au@Fe3O4 NPs can produce a blue colored solution in the presence of 3,3',5,5'-tetramethylbenzidine and H2O2. When the reaction was terminated by addition of H(+) ions, the blue product could be changed into a yellow one with higher absorption intensity. This colorimetric aptasensor can detect as low as 30 pgmL(-1) OTA with high specificity. To the best of our knowledge, the present colorimetric aptasensor is the first attempt to use the peroxidase-like activity of nanomaterial for OTA detection, which may provide an acttractive path toward routine quality control of food safety. Copyright © 2015 Elsevier B.V. All rights reserved.

  7. Core-shell Fe3O4 polydopamine nanoparticles serve multipurpose as drug carrier, catalyst support and carbon adsorbent.

    Science.gov (United States)

    Liu, Rui; Guo, Yunlong; Odusote, Gloria; Qu, Fengli; Priestley, Rodney D

    2013-09-25

    We present the synthesis and multifunctional utilization of core-shell Fe3O4 polydopamine nanoparticles (Fe3O4@PDA NPs) to serve as the enabling platform for a range of applications including responsive drug delivery, recyclable catalyst support, and adsorbent. Magnetite Fe3O4 NPs formed in a one-pot process by the hydrothermal approach were coated with a polydopamine shell layer of ~20 nm in thickness. The as prepared Fe3O4@PDA NPs were used for the controlled drug release in a pH-sensitive manner via reversible bonding between catechol and boronic acid groups of PDA and the anticancer drug bortezomib (BTZ), respectively. The facile deposition of Au NPs atop Fe3O4@PDA NPs was achieved by utilizing PDA as both the reducing agent and the coupling agent. The nanocatalysts exhibited high catalytic performance for the reduction of o-nitrophenol. Furthermore, the recovery and reuse of the catalyst was demonstrated 10 times without any detectible loss in activity. Finally, the PDA layers were converted into carbon to obtain Fe3O4@C and used as an adsorbent for the removal of Rhodamine B from an aqueous solution. The synergistic combination of unique features of PDA and magnetic nanoparticles establishes these core-shell NPs as a versatile platform for multiple applications.

  8. Synthesis,M(o)ssbauer Spectra and Magnetic Properties of Quasi-One-Dimensional Fe3O4 Nanowires

    Institute of Scientific and Technical Information of China (English)

    薛德胜; 张丽英; 高存绪; 许雪飞; 桂安标

    2004-01-01

    Quasi-one-dimensional Fe3O4 nanowires in diameter of about 200nm were assembled into anodic aluminium oxide templates via electrodepositing and heat-treating processes. The nanowires have a polycrystalline spinel structure with a = 8.317A, and each nanowire is composed of fine Fe3O4 crystallites with size of about 30nm.The magnetic moments of Fe3 O4 crystallites in nanowires have a preferred orientation leaning to the wire axis but not parallel to the wire axis. Mossbauer spectra (MS) were used to verify the presence of Fe3 O4 further and the existence of superparamagnetic particles in nanowires. A perpendicular magnetic anisotropy was observed obviously. Temperature dependence of the magnetic moments (M-T) shows that the Verwey transition for the Fe3 O4 nanowires occurs at 50 K, and the behaviour of the M-T curve is different from that of other magnetite materials. These characteristic magnetic properties of Fe3 O4 nanowires are mainly due to the reduced dimension and the configuration of preferred orientation in the nanowires caused by the shape anisotropy.

  9. Synthesis and Characterization of Magnetic Elastomer based PEG-Coated Fe3O4 from Natural Iron Sand

    Science.gov (United States)

    Kurniawan, C.; Eko, A. S.; Ayu, Y. S.; Sihite, P. T. A.; Ginting, M.; Simamora, P.; Sebayang, P.

    2017-05-01

    Magnetic elastomer nanocomposite based PEG-coated Fe3O4 with silicone rubber binder have been prepared from natural iron-sand by using coprecipitation method. The samples were characterized by using X-ray Diffractometer, X-ray Fluorescence, Fourier Transform Infra-Red, tensile strength test, and Vibrating Sample Magnetometer to analyze the physical and magnetic properties. We observed that all samples were formed by single phase cubic spinel magnetite (Fe3O4) crystalline structure. The atomic bonding analysis by FTIR showed that the C-O-C and C-H ordering were understood as the PEG - Fe3O4 bonding characteristics. We have observed that the Young modulus of elastomer based PEG-coated Fe3O4 slightly decreased compared to the natural iron-sand based elastomer. The magnetic properties of PEG-coated Fe3O4 were known to be magnetically softer with the lowest coercivity without losing its magnetization saturation value. We propose that the PEG-coated Fe3O4 is a promising candidate to be applied as magnetorheological elastomer due to a good mechanical and magnetic characteristic and also promising as microwave absorbing materials.

  10. Heterogenized Bimetallic Pd-Pt-Fe3O4 Nanoflakes as Extremely Robust, Magnetically Recyclable Catalysts for Chemoselective Nitroarene Reduction.

    Science.gov (United States)

    Byun, Sangmoon; Song, Yeami; Kim, B Moon

    2016-06-15

    A very simple synthesis of bimetallic Pd-Pt-Fe3O4 nanoflake-shaped alloy nanoparticles (NPs) for cascade catalytic reactions such as dehydrogenation of ammonia-borane (AB) followed by the reduction of nitro compounds (R-NO2) to anilines or alkylamines (R-NH2) in methanol at ambient temperature is described. The Pd-Pt-Fe3O4 NPs were easily prepared via a solution phase hydrothermal method involving the simple one-pot coreduction of potassium tetrachloroplatinate (II) and palladium chloride (II) in polyvinylpyrrolidone with subsequent deposition on commercially available Fe3O4 NPs. The bimetallic Pd-Pt alloy NPs decorated on Fe3O4 NPs provide a unique synergistic effect for the catalysis of cascade dehydrogenation/reduction. Various nitroarene derivatives were reduced to anilines with very specific chemoselectivity in the presence of other reducible functional groups. The bimetallic Pd-Pt-Fe3O4 NPs provide a unique synergistic effect for the catalysis of cascade dehydrogenation/reduction. The nitro reduction proceeded in 5 min with nearly quantitative conversions and yields. Furthermore, the magnetically recyclable nanocatalysts were readily separated using an external magnet and reused up to 250 times without any loss of catalytic activity. A larger scale (10 mmol) reaction was also successfully performed with >99% yield. This efficient, recyclable Pd-Pt-Fe3O4 NPs system can therefore be repetitively utilized for the reduction of various nitro-containing compounds.

  11. Contribution of Fe3O4 nanoparticles to the fouling of ultrafiltration with coagulation pre-treatment

    Science.gov (United States)

    Yu, Wenzheng; Xu, Lei; Graham, Nigel; Qu, Jiuhui

    2015-08-01

    A coagulation (FeCl3)-ultrafiltration process was used to treat two different raw waters with/without the presence of Fe3O4 nanoparticle contaminants. The existence of Fe3O4 nanoparticles in the raw water was found to increase both irreversible and reversible membrane fouling. The trans-membrane pressure (TMP) increase was similar in the early stages of the membrane runs for both raw waters, while it increased rapidly after about 15 days in the raw water with Fe3O4 nanoparticles, suggesting the involvement of biological effects. Enhanced microbial activity with the presence of Fe3O4 nanoparticles was evident from the measured concentrations of extracellular polymeric substances (EPS) and deoxyribonucleic acid (DNA), and fluorescence intensities. It is speculated that Fe3O4 nanoparticles accumulated in the cake layer and increased bacterial growth. Associated with the bacterial growth is the production of EPS which enhances the bonding with, and between, the coagulant flocs; EPS together with smaller sizes of the nano-scale primary particles of the Fe3O4-CUF cake layer, led to the formation of a lower porosity, more resilient cake layer and membrane pore blockage.

  12. Preparation and Characterization of Fe3O4/Ethiodized-oil Magnetic Fluids Used in Arterial Embolization Hyperthermia

    Institute of Scientific and Technical Information of China (English)

    罗志; 王益明; 洪若瑜; 李洪钟

    2012-01-01

    Fe3O4 nanoparticles (NPs) were prepared by the co-precipitation of Fe3+ and Fe2+ with ammonium hydroxide, and were modified by four different surfactants. The modified Fe3O4 NPs were characterized by Fourier transform infrared spectroscopy, X-ray powder diffraction, transmission electron microscopy and vibrating sample magne- tometer. Then, the modified Fe3O4 NPs were dispersed in ethiodized-oil by mechanical agitation and ultrasonic vi- bration to obtain stable Fe3O4 /ethiodized-oil magnetic fluids (MFs). The magnetic properties and rheological prop- erties of the MFs were measured using a Gouy magnetic balance and a rotational rheometer, respectively. The satu- ration magnetization of the Fe3O4 modified by oleic acid was 52.1 Emu/g. Furthermore, the result showed that the inductive heating effect of oleic acid stabilized Fe3O4/ethiodized-oil MF was remarkable and it only took 650 s for the temperature rising from 25 ℃ to 65 ℃. The specific absorption rate of the MF was 50.16 W/(g of Fe). It had a potential application in arterial embolization hyperthermia.

  13. Polydopamine-Encapsulated Fe3O4 with an Adsorbed HSP70 Inhibitor for Improved Photothermal Inactivation of Bacteria.

    Science.gov (United States)

    Liu, Dongdong; Ma, Liyi; Liu, Lidong; Wang, Lu; Liu, Yuxin; Jia, Qi; Guo, Quanwei; Zhang, Ge; Zhou, Jing

    2016-09-21

    Photothermal treatment, a new approach for inactivation of bacteria and pathogens that does not depend on traditional therapeutic approaches, has recently received much attention. In this study, a new type of nanoplatform (PDA@Fe3O4 + PES) was fabricated by using polydopamine (PDA, a photothermal conversion agent) to encapsulate Fe3O4 (a magnetic nanoparticle) and support 2-phenylethynesulfonamide (PES, an inhibitor of heat shock protein 70 (HSP70)). Upon near-infrared light irradiation, the increased temperature weakens π-π and hydrogen bonding interactions, and PES is released from the PDA@Fe3O4 + PES. The released PES inhibits the function of HSP70, reducing bacterial tolerance to photothermal therapy and improving the therapeutic effect against infectious bacterial pathogens. After treatment, PDA@Fe3O4 + PES can be recovered using the magnetic property of the Fe3O4 cores. Consequently, PDA@Fe3O4 + PES possesses the potential to be a recyclable photothermal agent for enhanced photothermal bacterial inactivation without causing secondary pollution.

  14. Fe(3)O(4)@Au/polyaniline multifunctional nanocomposites: their preparation and optical, electrical and magnetic properties.

    Science.gov (United States)

    Yu, Qiaozhen; Shi, Minmin; Cheng, Yunan; Wang, Mang; Chen, Hong-Zheng

    2008-07-02

    Fe(3)O(4)@Au/polyaniline (PANI) nanocomposites were fabricated by in situ polymerization in the presence of mercaptocarboxylic acid. The mercaptocarboxylic acid was used to introduce hydrogen bonding and/or electrostatic interaction; it acts as a template in the formation of Fe(3)O(4)@Au/PANI nanorods. The morphology and structure of the resulting nanocomposites were analyzed by scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy, x-ray diffraction and x-ray energy dispersion spectroscopy (EDS). It was found that the nanocomposites were rod-like with an average diameter of 153 nm, and they exhibited a core-shell structure. A UV-visible spectrometer, semiconductor parameter analyzer and vibrating sample magnetometer (VSM) were used to characterize the optical, electrical and magnetic properties of the Fe(3)O(4)@Au/PANI nanocomposites. It was interesting to find that these properties are dependent on the molar ratio of Au to Fe(3)O(4) when the molar ratio of Fe(3)O(4)@Au to PANI is fixed. The magnetic property of the Fe(3)O(4)@Au/PANI nanocomposite is very close to superparamagnetic behavior.

  15. High surface area monodispersed Fe3O4 nanoparticles alone and on physical exfoliated graphite for improved supercapacitors

    Science.gov (United States)

    Sarno, Maria; Ponticorvo, Eleonora; Cirillo, Claudia

    2016-12-01

    Highly conductive, unsophisticated and easy to be obtained physical exfoliated graphite (PHG) supporting well dispersed magnetite, Fe3O4/PHG nanocomposite, has been prepared by a one-step chemical strategy and physico-chemical characterized. The nanocomposite, favoured by the a-polar nanoparticles (NPs) capping, results in a self-assembled monolayer of monodispersed Fe3O4, covering perfectly the hydrophobic surfaces of PHG. The nanocomposite as an electrode material was fabricated into a supercapacitor and characterized by cyclic voltammetry (CV) and galvanostatic charge-discharge measurements. It shows, after a suitable annealing, significant electrochemical properties (capacitance value of 787 F/g at 0.5 A g-1 and a Fe3O4/PHG weight ratio of 0.31) and good cycling stability (retention 91% after 30,000 cycles). Highly monodispersed very fine Fe3O4 NPs, covered by organic chains, have been also synthesized. The high surface area Fe3O4 NPs, after washing to leave a low content of organic chains able to avoid aggregation without excessively affecting the electrical properties of the material, exhibit remarkable pseudocapacitive activities, including the highest specific capacitance over reported for Fe3O4 (300 F/g at 0.5 A g-1).

  16. Efficient purification of lysozyme from egg white by 2-mercapto-5-benzimidazolesulfonic acid modified Fe3O4/Au nanoparticles.

    Science.gov (United States)

    Zhu, Xinjun; Zhang, Lianying; Fu, Aiyun; Yuan, Hao

    2016-02-01

    2-Mercapto-5-benzimidazolesulfonic acid (MBISA) modified Fe3O4/Au nanoparticles were synthesized in aqueous solution and characterized by photo correlation spectroscopy (PCS) and vibrating sample magnetometer (VSM). The so-obtained Fe3O4/Au-MBISA nanoparticles were capable of specific adsorbing lysozyme. The maximum amount of lysozyme adsorbed on 1.0mg Fe3O4/Au-MBISA nanoparticles was 346μg. The lysozyme desorption behavior was studied and the lysozyme recovery from Fe3O4/Au-MBISA nanoparticles approached 100% under optimal conditions, and the reusability studies showed that the nanoparticles could maintain about 91% of the initial lysozyme adsorption capacity after 7 repeated adsorption-elution cycles. The Fe3O4/Au-MBISA nanoparticles were used in the purification of lysozyme from chicken egg white, which was verified by a single SDS-PAGE band. Therefore, the obtained Fe3O4/Au-MBISA nanoparticles exhibited excellent performance in the direct purification of lysozyme from egg white.

  17. Magnetic alignment of SWCNTs decorated with Fe3O4 to enhance mechanical properties of SC-15 epoxy

    Directory of Open Access Journals (Sweden)

    O. Malkina

    2013-04-01

    Full Text Available We report significant improvement in mechanical properties of SC-15 epoxy when reinforced with decorated nanotubes and cured in a modest magnetic field. The chemical synthesis and field curing process is a low cost and relatively easy technique to impose strong magnetic anisotropy into the system without the need of a superconducting magnet. SWCNT(COOHs were decorated with Fe3O4 nanoparticles through a sonochemical oxidation process and then dispersed into SC-15 epoxy at 0.5 wt% loading. The admixture was cured for 6 hours in a magnetic field of 10 kOe followed by an additional 24 hours of post curing at room temperature. Control samples were prepared in a similar manner but without the application of the magnetic field. Mechanical tests performed on field-cured samples indicated that tensile strength and modulus increased by 62% and 40%. Most importantly, modulus of toughness, fracture strain, and modulus of resilience improved by 346%, 165%% and 170%, respectively. Such enhancement in mechanical properties was attributed to changes in polymer morphology, partial alignment of nanotubes in the field direction, and sliding at the polymer-nanotube interface. Detailed characterization of the system with XRD, TEM, DMA, and Magnetometry are described in the paper.

  18. Alpha chymotrypsin coated clusters of Fe3O4 nanoparticles for biocatalysis in low water media

    Directory of Open Access Journals (Sweden)

    Mukherjee Joyeeta

    2012-11-01

    Full Text Available Abstract Background Enzymes in low water containing non aqueous media are useful for organic synthesis. For example, hydrolases in such media can be used for synthetic purposes. Initial work in this area was carried out with lyophilized powders of enzymes. These were found to have poor activity. Drying (removing bulk water by precipitation turned out to be a better approach. As enzymes in such media are heterogeneous catalysts, spreading these precipitates over a large surface gave even better results. In this context, nanoparticles with their better surface to volume ratio provide obvious advantage. Magnetic nanoparticles have an added advantage of easy separation after the reaction. Keeping this in view, alpha chymotrypsin solution in water was precipitated over a stirred population of Fe3O4 nanoparticles in n-propanol. This led to alpha chymotrypsin activity coated over clusters of Fe3O4 nanoparticles. These preparations were found to have quite high transesterification activity in low water containing n-octane. Results Precipitation of alpha chymotrypsin over a stirred suspension of Fe3O4 nanoparticles (3.6 nm diameter led to the formation of enzyme coated clusters of nanoparticles (ECCNs. These clusters were also magnetic and their hydrodynamic diameter ranged from 1.2- 2.6 microns (as measured by dynamic light scattering. Transmission electron microscopy (TEM, showed that these clusters had highly irregular shapes. Transesterification assay of various clusters in anhydrous n-octane led to optimization of concentration of nanoparticles in suspension during precipitation. Optimized design of enzyme coated magnetic clusters of nanoparticles (ECCN 3 showed the highest initial rate of 465 nmol min-1 mg-1protein which was about 9 times higher as compared to the simple precipitates with an initial rate of 52 nmol min-1 mg-1 protein. Circular Dichroism (CD(with a spinning cell accessory showed that secondary structure content of the alpha

  19. Temperature dependence of the spin relaxation time of Fe3O4 and hemozoin superparamagnetic nanocrystals

    Science.gov (United States)

    Khmelinskii, I.; Makarov, V.

    2017-08-01

    We report experimental temperature and concentration dependences of the natural spin relaxation time of superparamagnetic Fe3O4 and hemozoin nanocrystals. We recorded the 1H NMR spectrum of 0.5% benzene dissolved in CS2 in function of superparamagnetic particle concentration and temperature, interpreting the 7.261 ± 0.002 ppm benzene line broadening. Our model for the line broadening includes natural, hyperfine magnetic dipole-dipole, and contact hyperfine contributions. The latter arises due to exchange interaction between benzene molecules and suspended nanoparticles. Estimated frequency of fluctuation in the 1 cm3 sample volume is in the 107 Hz scale. Estimated natural electron spin-lattice relaxation frequencies of the superparamagnetic nanocrystals using frequency of fluctuations, and developed theoretical model applied to analysis of experimental data are in good agreement between each other. Thus the presently developed approach may be used to study fluctuations and natural spin-lattice relaxation frequencies in different media.

  20. Hydrodynamic Properties of Fe3O4 Kerosene-Based Ferrofluids with Narrow Particle Size Distribution

    Institute of Scientific and Technical Information of China (English)

    ZHANG Jian-Hui; XU Xue-Fei; SI Ming-Su; ZHOU You-He; XUE De-Sheng

    2005-01-01

    @@ We investigate the hydrodynamic properties of Fe3O4 kerosene-based ferrofluids with narrow particle size distri-bution. The ferrofluids are synthesized by improving chemical coprecipitation technique. A narrow distribution of 8.6-10.8nm particle sizes is obtained from the magnetization curve with the free-form model based on the Bayesian inference theory. The fitting result is consistent with average particle size obtained from x-ray diffraction. With the increase of applied magnetic field and magnetic particle concentration, apparent viscosity of ferrofluids increases. At concentration 4.04%, the type of flow for the ferrofluid transforms from Newtonian to Bingham plastic fluid as the applied magnetic field increases.

  1. Magnetite Fe3O4 (111) Surfaces: Impact of Defects on Structure, Stability, and Electronic Properties

    KAUST Repository

    Noh, Junghyun

    2015-08-04

    We present a comprehensive investigation, via first-principles density functional theory (DFT) calculations, of various surface terminations of magnetite, Fe3O4 (111), a major iron oxide which has also a number of applications in electronics and spintronics. We compare the thermodynamic stability and electronic structure among the different surfaces terminations. Interestingly, we find that surfaces modified with point defects and adatoms can be more stable than bulk-like terminations. These surfaces show different surface chemistry, electronic structures and distinctive spin polarization features near the Fermi level from those previously considered in the literature. Our studies provide an atomic level insight for magnetite surfaces, which is a necessary step to understanding their interfaces with organic layers in OLED and spintronic devices.

  2. Green synthesis of magnetite (Fe3O4) nanoparticles using Graptophyllum pictum leaf aqueous extract

    Science.gov (United States)

    Sari, I. P.; Yulizar, Y.

    2017-04-01

    Magnetite nanoparticles (MNPs) attracted the attention of many researchers due to their unique properties. In this research, nanoscale magnetite particles have been successfully synthesized through an environmentally friendly method using aqueous extract of Graptophyllum pictum leaf (GPLE). In MNPs formation, GPLE acted as a base source and capping agent. Alkaloids in GPLE were hydrolyzed in water and hydroxilated Fe2+ to form Fe3O4 nanoparticles powder through calcination. After the addition of leaf extract, MNPs formation was observed by color change from pale yellow to dark brown. The synthesized nanoparticles were characterized using UV-Vis spectrophotometer, X-Ray diffraction (XRD), and Fourier transform infra red (FTIR) spectroscopy. The results confirmed that MNPs formation indicated the surface plasmon resonance at a maximum wavelength, λmax 291 nm. The average crystallite size is 23.17 nm. The formed MNPs through green synthesis method promise in various medical applications such as drug carrier and targeted therapy.

  3. Facile synthesis and characterization of magnetochromatic Fe3O4 nanoparticles

    Science.gov (United States)

    Wang, Wei; Zheng, Lelin; Lu, Fenghua; Hong, Ruijiang; Chen, Michael Z. Q.; Zhuang, Lin

    2017-05-01

    A facile synthetic method for magnetochromatic Fe3O4 nanoparticles (FNPs) with controllable size and optical properties has been fabricated by the combination of an improved solvothermal method and the usage of ultrasonic irradiation in the surface modification step. The improved solvothermal method enables the alteration of the size of nanopar