Preparation and photocatalytic properties of silver nanoparticles loaded on CNTs/TiO2 composite

In this study, new nanoscale photocatalyst based on silver and CNTs/TiO₂ was successfully prepared by photoreduction method. The prepared Ag-CNTs/TiO₂ was characterized by TEM, XRD and XPS. The photocatalytic activity was also evaluated by photocatalytic degradation of Reactive Brilliant Red X-3B dye. The results indicated that the photocatalytic efficiency of CNTs/TiO₂ increased in the presence of Ag nanoparticles and the photocatalysis reaction followed a first order kinetics. The kinetic constant of Ag-CNTs/TiO₂ for dye degradation was nearly 1.2 times than that of CNTs/TiO₂, which indicated decorating Ag nanoparticles on CNTs/TiO₂ could enhance the photocatalytic ability.     

Preparation and characterization of biocompatible magnetic carbon nanotubes

Magnetic carbon nanotubes consisting of multi-wall carbon nanotubes (MWNTs) core and Fe₃O₄ shell were successfully prepared by in situ thermal decomposition of Fe(acac)₃ or FeCl₃ or Fe(CO)₅ in 2-pyrrolidone containing acid treated MWNTs at 240 °C with the protection of nitrogen gas. The samples were characterized by TEM, XRD, SEAD, XPS and superconducting quantum interference device. Also, their biocompatibility was compared with naked carbon nanotubes. The results showed that after coated with Fe₃O₄ nanoparticles, the obtained magnetic carbon nanotubes show superparamagnetic characteristic at room temperature, and their blocking temperature is about 80 K. The magnetic properties of the nanotubes are relevant to the content of magnetic particles, increasing content of magnetic nanoparticles leads to higher blocking temperature and saturation magnetization. The results of antimicrobial activities to bacterial cells (Escherichia coli) showed that the MWNTs have antimicrobial activity, while the magnetic nanotubes are biocompatible even with a higher concentration than that of MWNTs.     

Hydrothermal synthesis of graphene oxide/multiwalled carbon nanotube/Fe<Subscript>3</Subscript>O<Subscript>4</Subscript> ternary nanocomposite for removal of Cu (II) and methylene blue

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.     

Electrostatic self-assembly of Fe3O4 nanoparticles on carbon nanotubes

Carbon nanotubes (CNTs)-based magnetic nanocomposites can find numerous applications in nanotechnology, integrated functional system, and in medicine owing to their great potentialities. Herein, densely distributed magnetic Fe₃O₄ nanoparticles were successfully attached onto the convex surfaces of carbon nanotubes (CNTs) by an in situ polyol-medium solvothermal method via non-covalent functionalization of CNTs with cationic surfactant, cetyltrimethylammonium bromide (CTAB), and anionic polyelectrolyte, poly(sodium 4-styrenesulfonate) (PSS), through the polymer-wrapping technique, in which the negatively charged PSS-grafted CNTs can be used as primer for efficiently adsorption of positively metal ions on the basis of electrostatic attraction. X-ray diffractometry (XRD), X-ray photoelectron spectroscopy (XPS) and transmission electron microscopy (TEM) analysis have been used to study the formation of Fe₃O₄/CNTs. The Fe₃O₄/CNTs nanocomposites were proved to be superparamagnetic with saturation magnetization of 43.5 emu g^?1. A mechanism scheme was proposed to illustrate the formation process of the magnetic nanocomposites.     

Solvothermal one-step synthesis of MWCNTs/Ni0.5Zn0.5Fe2O4 magnetic composites

A magnetic multi-walled carbon nanotubes-based (MWCNTs-based) composite, MWCNTs/Ni_0.5Zn_0.5Fe₂O₄, was synthesized via a facile solvothermal approach. The composites were characterized by X-ray diffraction analysis, transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), and vibrating sample magnetometry. The results confirmed that MWCNTs and Ni_0.5Zn_0.5Fe₂O₄ coexisted in the composites. The TEM and HRTEM results showed a thick layer of Ni_0.5Zn_0.5Fe₂O₄ was intimately connected to the surface of MWCNTs. The saturation magnetization value of the composites was 45.8 emu/g. Furthermore, the probable synthesis mechanism of the magnetic composites was also investigated based on the experimental results.     

Synthesis of Fe3O4/CNTs magnetic nanocomposites at the liquid-liquid interface using oleate as surfactant and reactant

Carbon nanotubes (CNTs)-based magnetic nanocomposites have attracted significant research interest owing to their great potentialities in various technological fields. In this investigation, a kind of novel Fe₃O₄/CNTs magnetic nanocomposites were prepared by in situ chemical precipitation using oleate as reactant and surfactant at the liquid-liquid interface of cyclohexane/ethanol/water mixture solvent. The as-prepared samples were characterized via transmission electron microscopy (TEM), X-ray diffractometry (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared (FTIR) and vibration sample magnetometry (VSM). Results indicated that the Fe₃O₄/CNTs magnetic nanocomposites dispersed well in organic medium were prepared organic medium, were prepared. The magnetic nanocomposites were proved to be superparamagnetic with coercive force of 3.69 Oe. A mechanism scheme was proposed to illustrate the formation process of the magnetic nanocomposites.     

Green synthesis and characterization of superparamagnetic Fe3O4 nanoparticles

In this paper, we have first demonstrated a facile and green synthetic approach for preparing superparamagnetic Fe₃O₄ 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 Fe₃O₄ was obtained. The scanning electron microscopy (SEM) and transmission electron microscopy (TEM) results exhibited that Fe₃O₄ 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 Fe₃O₄ obtained from the JCPDS database. The superconducting quantum interference device (SQUID) results revealed that the blocking temperature (T_b) 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 Fe₃O₄ 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 Fe₃O₄. This method might provide a new, mild, green, and economical concept for the synthesis of other nanomaterials.     

Synthesis of carbon nanotubes via Fe-catalyzed pyrolysis of phenolic resin

Carbon nanotubes (CNTs) with 40–100 nm in diameter and tens of micrometers in length were prepared via catalytic pyrolysis of phenol resin in Ar at 673–1273 K using ferric nitrate as a catalyst precursor. Structure and morphology of pyrolyzed resin were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and Raman spectroscopy. Ferric nitrate was transformed to Fe₃O₄ at 673 K, and to metallic Fe and Fe_xC carbide at 873–1273 K. The optimal weight ratio of Fe catalyst to phenol resin for growing CNTs was 1.00 wt%, and the optimal temperature was 1073 K. In addition, use of a high pressure increased the yield of CNTs. Density functional theory (DFT) calculations suggest that Fe catalysts facilitate the CNTs growth by increasing the bond length and weakening the bond strength in C₂H₄ via donating electrons to the C atoms in it.     

Magnetic nanoparticles coated with polysaccharide polymers for potential biomedical applications

This study reports a two-steps route for obtaining magnetic nanoparticles–polysaccharide hybrid materials consisting of Fe₃O₄, NiFe₂O₄ and CuFe₂O₄ nanoparticles synthesis by coprecipitation method in the presence of a soft template followed by coating of ferrite nanoparticles of 8–10-nm size range with polysaccharide type polymers—sodium alginate or chitosan. Magnetic oxide nanoparticles and the corresponding hybrid materials were characterized by X-ray diffraction (XRD), Mössbauer spectroscopy, atomic absorption spectroscopy (AAS), FTIR spectroscopy, scanning and transmission electron microscopy (SEM and TEM) and specific surface area measurements. The vibrating sample magnetometry confirms the superparamagnetic properties of the synthesized ferrites and hybrids. Using this route, the percent of magnetic nanoparticles retained in chitosan-based hybrid materials is nearly double in comparison with that of sodium alginate–based materials. The biological activity tests on Escherichia coli ATCC 25922, Pseudomonas aeroginosa ATCC 27853, Staphylococcus aureus ATCC 25923 and Candida scotti microorganisms show the non-toxic properties of prepared hybrid materials.     

Synthesis of carbon nanotubes and iron oxide nanoparticles in MW plasma torch with Fe(CO)5 in gas feed

The MW plasma torch (2.45 GHz) in the mixture of CH₄/H₂/Ar (42/430/1540 sccm) with added Fe(CO)₅vapors was used for the synthesis of iron oxide nanoparticles and carbon nanotubes. The particles with well-defined facets consisting of Fe₃O₄ and -Fe₂O₃ and self-assembled into long chains were produced at the power of 360 W. At higher power of 440-460 W the deposit contained significant amount of multi-walled carbon nanotubes covered by iron oxide nanoparticles. The diameter of CNTs was 8-20 nm. The particles had Fe₃O₄ and/or -Fe₂O₃ cores of spherical shape covered by a thin layer of carbon.     

Pyridine-thermal synthesis and high catalytic activity of CeO2/CuO/CNT nanocomposites

Carbon nanotubes (CNTs) were controllably coated with the uninterrupted CuO and CeO₂ composite nanoparticles by a facile pyridine-thermal method and the high catalytic performance for CO oxidation was also found. The obtained nanocomposites were characterized by transmission electron microscopy, scanning electron microscopy, X-ray diffraction as well as X-ray photoelectron spectroscopy. It is found that the CuO/CeO₂ composite nanoparticles are distributed uniformly on the surface of CNTs and the shell of CeO₂/CuO/CNT nanocomposites is made of nanoparticles with a diameter of 30-60 nm. The possible formation mechanism is suggest as follows: the surface of CNTs is modified by the pyridine due to the π-π conjugate role so that the alkaline of pyridine attached on the CNT surface is more enhanced as compared to the one in the bulk solvent, and thus, these pyridines accept the proton from the water molecular preferentially, which result in the formation of the OH⁻ ions around the surface of CNTs. Subsequently, the metal ions such as Ce³⁺ and Cu²⁺ in situ react with the OH⁻ ions and the resultant nanoparticles deposit on the surface of CNTs, and finally the CeO₂/CuO/CNT nanocomposites are obtained. The T₅₀ depicting the catalytic activity for CO oxidation over CeO₂/CuO/CNT nanocomposites can reach ∼113 °C, which is much lower than that of CeO₂/CNT or CuO/CNT nanocomposites or CNTs.     

海藻酸改性的空心Fe3O4纳米颗粒的制备与应用

不使用任何模板一步制得空心Fe₃O₄纳米颗粒,然后将海藻酸钠嫁接在氨基化的空心Fe₃O₄表面,再利用海藻酸盐与钙离子的作用,在空心Fe₃O₄表面形成一个凝胶化层,制得海藻酸盐凝胶化的空心Fe₃O₄纳米颗粒,粒径约为400～500 nm．采用TEM、XRD、XPS、VSM等手段对纳米微球进行表征．VSM表征结果表明在室温下样品磁性材料为超顺磁性．改性Fe₃O₄纳米颗粒成功地用于柔红霉素的载负和缓释,最大载负率和载药量分别为28.4%和14.2%．缓释结果表明,海藻酸盐凝胶化层的存在,能更有效控制柔红霉素缓慢地释放．     

High performance magnetic elastomer nanocomposites

Elastomer nanocomposites were prepared by mixing carbon nanofiber (CNF) decorated with metal nanoparticles (CNF–Fe₂O₃) with latex. The Fe₂O₃ metal nanoparticles were decorated on the CNF by electrostatic attraction via a green and facile solution-based method. The presence of the metal nanoparticles on the surface of the CNF improved their dispersion and electric contact resistance in the elastomer matrix. Interestingly, the CNF–Fe₂O₃/elastomer composite exhibited improvements in both tensile strength and elongation (carbon black/elastomer), by as much as 9.7 and 28.9%, respectively, compared to an elastomer control without filler. Also, the CNF–Fe₂O₃/elastomer exhibited superior thermal and electrical conductivity compared with the control. In an applied magnetic field the elastomer nanocomposites showed a significant transition from dominant diamagnetism to ferromagnetism due to synergies between the Fe₂O₃ nanoparticles and the CNF. The elastomer nanocomposites prepared with CNF–Fe₂O₃ will open significant new opportunities for preparing advanced elastomer nanocomposites for future engineering applications.     

PVDF/PS/HDPE/MWCNTs/Fe3O4 nanocomposites: Effective and lightweight electromagnetic interference shielding material through the synergetic effect of MWCNTs and Fe3O4 nanoparticles

In this work, Polyvinylidene Fluoride (PVDF)/polystyrene (PS)/high density polyethylene (HDPE) ternary blends displayed a core-shell structure where HDPE was the core, PS was the shell, and this core-shell system dispersed in PVDF matrix. Here, multiwall carbon nanotubes (MWCNTs) and ferroferric oxide (Fe₃O₄) was incorporated. F-F composites with MWCNTs was in PS shell and Fe₃O₄ was in PVDF matrix and E-F composites with MWCNTs was in PS shell and Fe₃O₄ was in HDPE core were fabricated by melt blending. It was indicated that the core-shell morphology between PS and HDPE was well retained with the incorporation of Fe₃O₄ and MWCNTs. Both the electrical conductivity of F-F and E-F composites were similar without no obvious change with the incorporation of Fe₃O₄. Composites with greater than 20 dB shielding effectiveness were easy to obtain. The highest SE we observed was for the F-F composite with 1 vol% Fe₃O₄ and 1 vol% MWCNTs was 25 dB at 9.5 GHz, and the SE was over 20 dB in the whole measured frequency(X-band). The E-F composites with SE greater than 20 dB in X-band was at 2 vol% Fe₃O₄ and 1 vol% MWNCTs. Such effective and lightweight nanocomposites were obtained, resulting from the synergetic effect of MWCNTs and Fe₃O₄ nanoparticles.     

Green synthesis of soya bean sprouts-mediated superparamagnetic Fe3O4 nanoparticles

Superparamagnetic Fe₃O₄ 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 Fe₃O₄ nanoparticles was investigated using X-ray photoemission spectroscopy (XPS) and Fourier-transform infrared spectroscopy (FT-IR). The results indicate that spherical Fe₃O₄ 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 Fe₃O₄ nanoparticles. In addition, the superconducting quantum interference device (SQUID) results indicate the products are superparamagnetic at room temperature, with blocking temperature (T_B) of 150 K and saturation magnetization of 37.1 emu/g.     

One‐Dimensional Magnetic Composite of Polypyrrole‐Containing Carbon Nanotubes/Ni0.75Zn0.25Fe2O4

A novel one‐dimensional electromagnetic nanocomposite of polypyrrole (PPY) containing carbon nanotubes (CNTs)/Ni_0.75Zn_0.25Fe₂O₄ was synthesized by an in‐situ polymerization method. The composite was characterized by x‐ray diffraction (XRD), transmission electron microscopy (TEM), high resolution transmission electron microscopy (HRTEM) and Fourier transform infrared. The XRD results confirmed that PPY, CNTs, and Ni_0.75Zn_0.25Fe₂O₄ coexisted in the composite. The TEM and HRTEM results indicated that PPY coated the surface of the CNTs/Ni_0.75Zn_0.25Fe₂O₄ with a thickness of 15–30 nm. The lattice spacings, according to the first main peak of the CNTs, Ni_0.75Zn_0.25Fe₂O₄, and PPY, was about 0.34 nm, 0.25 nm, and 0.42 nm, respectively. The FTIR result also indicated that the PPY formed in the composite. A test of magnetic properties indicated that the composite was ferromagnetic with the saturated magnetization of 12.86 electromagnetic units (emu)/g, and the coercive of 127.18 Oersted (Oe).     

Synthesis and characteristics of multifunctional Fe3O4-SiO2-CdS magnetic-fluorescent nanocomposites

A luminescent superparamagnetic nanocomposite with an Fe 3 O 4-SiO 2-CdS structure is synthesized.Coated with a silica shell,Fe 3 O 4 nanoparticles and CdS quantum dots (QDs) are successfully assembled together.Analysed from the test results of X-ray diffraction (XRD),transmission electron microscopy (TEM),high resolution transmission electron microscopy (HRTEM),hysteresis loop,and photoluminescence (PL) spectrum,these nanocomposites exhibit superparamagnetic and photoluminescent properties.     

Controlled-synthesis,characterization, and magnetic properties of Fe<Subscript>3</Subscript>O<Subscript>4</Subscript> nanostructures

Fe₃O₄ nanostructures with different morphologies, including uniform nanoparticles, nanorods and nanowire bundles, have been successfully synthesized via a facile hydrothermal route. Based on the observation of TEM images, the growth mechanism of one-dimensional Fe₃O₄ nanostructures is in accordance with Ostwald ripening process. From the hysteresis loops of as-prepared Fe₃O₄ products, we found that the morphology has great influence on the magnetic properties. The uniform Fe₃O₄ nanoparticles have higher saturation magnetization and lower coercivity than that of Fe₃O₄ nanorods and nanowires bundles. These phenomena attribute to the high shape anisotropy of nanorods and nanowire bundles, which prevent them from magnetizing in directions other than along their easy magnetic axes. PACS 81.07.-b; 75.50.Bb; 75.30.Gw; 81.10.Dn; 81.16.Be     

Preparation and characterization of silicon oil based ferrofluid

Stable silicon oil based ferrofluid was prepared in the present investigation. Silicon oil surfactant ethoxy terminated polydimethylsiloxane was used to modify the Fe₃O₄ nanoparticles. The Fe₃O₄ nanoparticles were firstly coated with a SiO₂ layer by the hydrolysis of tetraethoxysilane. Then using the active hydroxyl groups on the surface of the SiO₂, silicon oil surfactant was covalently grafted onto the Fe₃O₄ nanoparticles surface. The ethoxy terminated polydimethylsiloxane has similar molecular chain structure and good compatibility with that of the carrier liquid, thus ensuring stable dispersion of modified Fe₃O₄ in the carrier silicon oil. The interaction between Fe₃O₄ and the modifier was characterized by IR and XPS. The crystal structure and the magnetic properties of the Fe₃O₄ nanoparticles were determined by XRD and VSM, respectively. The size and morphology of the particles were observed using TEM. The properties of the silicon oil based ferrofluid were characterized by Gouy magnetic balance. The results indicated that the ferrofluid had high magnetism and good stability. The rheological properties and thermostability of the ferrofluid were also investigated.     

Synthesis of magnetite nanoparticles via a solvent-free thermal decomposition route

Superparamagnetic nanoparticles have been widely applied in various bio-medical applications. To date, it is still a challenge to synthesize nanosized Fe₃O₄ particles with controlled size and distribution. In this paper, a novel solvent-free thermal decomposition method is reported for synthesizing Fe₃O₄ nanoparticles. Size and morphology of the nanoparticles are determined by TEM while the structure of the nanoparticles is identified by FTIR, XPS and TGA measurements. Magnetic properties of the obtained particles are determined using VSM and SQUID measurement. The particle size of the Fe₃O₄ can be tailored by adjusting either reaction temperature or time. When the reaction temperature is increased to 330 °C and the reaction time is extended to 4 h, the average particle size of the obtained nanoparticles is ∼9 nm, while Ms value reaches ∼76 emu/g. The as synthesized Fe₃O₄ nanoparticles show well-established superparamagnetic properties with the blocking temperature at around 100 K.