Synthesis and solid-state structure of a Pt-Ru-P ternary metal phosphide (PtRuP2) as a carbon nanocomposite

Reactive thermal degradation of Pt(PPh3)(Cl)(mu2-Cl)2Ru(Cl)(eta3:eta3-C10H16)/Vulcan carbon powder composites gives a nanocomposite powder containing nanocrystals of the expected PtRu alloy phase along with nanocrystals of an unknown substance. Yields of the unknown phase increase when PPh3 is added to the composite prior to thermal treatment. The new substance has been identified as a ternary metal phosphide, PtRuP2. Full-profile Rietveld analysis of the XRD pattern of this phase is consistent with a primitive Pm3m cubic unit cell (CsCl-type) having a cell constant of 2.78 A. Fully disordered Pt and Ru atoms occupy the (0, 0, 0) atomic positions with P atoms occupying interstitial sites at the (1/2, 1/2, 1/2) atomic positions.     

Synthesis and characterization of PtSn/carbon and Pt3Sn/carbon nanocomposites as methanol electrooxidation catalysts

Two Pt-Sn/vulcan carbon nanocomposites containing nanoclusters of PtSn (niggliite) and Pt3Sn highly dispersed on a carbon powder support have been prepared using Pt(SnPh2Cl)(PPh3)2(Ph) or [Pt3[mu-(PPh2)2CH2]3(mu 3-SnF3) (mu 3-CO)][PF6] as single-source precursors of metal alloy. PtP2 or Pt metal is also present as a secondary phase. Bimetallic Pt-Sn nanoclusters with an average diameter of 5-8 nm are formed at a total metal loading of ca. 15 wt%. Evaluation of both Pt-Sn/C nanocomposites as electrooxidation catalysts in a direct methanol fuel cell gives fuel cell performances comparable to that expected for Pt-Sn catalysts prepared by more conventional methods.     

Rapid preparation of Pt-Ru/graphitic carbon nanofiber nanocomposites as DMFC anode catalysts using microwave processing

Pt-Ru/graphitic carbon nanofiber (GCNF) nanocomposites have been prepared on two different GCNF supports, with the use of a bimetallic precursor as a source of metal and microwave processing for thermal treatments. Pt-Ru nanoparticles appear as the major metal-containing component of these nanocomposites along with variable trace amounts of Ru metal. Use of microwave heating permits rapid preparation of these nanocomposites and affords metal nanoclusters of nearly uniform size. The performance of these nanocomposites as anode electrocatalysts in direct-methanol fuel cells (DMFCs) is compared with that of unsupported Pt-Ru colloid at identical total metal loading. The Pt-Ru/narrow tubular herringbone GCNF nanocomposite shows DMFC performance comparable to that recorded for an unsupported Pt-Ru colloid.     

One-step preparation of FeCo nanoparticles in a SBA-16 matrix as catalysts for carbon nanotubes growth

Nanocomposites containing FeCo alloy nanoparticles dispersed in a highly ordered 3D cubic Im3m mesoporous silica (SBA-16) matrix were prepared by a novel, single-step templated-assisted sol-gel technique. Two different approaches were used in the synthesis of nanocomposites; a pure SBA-16 sample was also prepared for comparison. Low-angle X-ray diffraction, transmission electron microscopy and N2 physisorption at 77 K show that after metal loading, calcination at 500 degrees C and reduction in H2 flux at 800 degrees C the nanocomposites retain the cubic mesoporous structure with pore size not very different from the pure matrix. X-ray absorption fine structure (EXAFS) analysis at Fe and Co K-edges demonstrates that the FeCo nanoparticles have the typical bcc structure. The final nanocomposites were tested as catalysts for the production of carbon nanotubes by catalytic chemical vapour deposition and high-resolution TEM shows that good quality multi-walled carbon nanotubes are obtained.     

Electrical and dielectric properties of polypropylene nanocomposites based on carbon nanotubes and barium titanate nanoparticles

Functional polypropylene (PP) nanocomposites were prepared by melt compounding with multiwalled carbon nanotubes (MWNT) as the electrically conductive component and barium titanate (BT) spherical nanoparticles as the ferroelectric component. To make PP electrically conductive, more than 3 wt.% MWNT is required. Surface modification of either MWNT or BT with titanate coupling agent further improves the electrical conductivity of the PP/MWNT/BT ternary nanocomposites. Interestingly, by modifying both MWNT and BT, 2 wt.% MWNT are sufficient to make the ternary nanocomposite electrically conductive. In addition, the incorporation of MWNT greatly increases the dielectric permittivity of PP/BT nanocomposites. However, to retain a low dielectric loss, the MWNT loading should be slightly less than the percolation threshold of the nanocomposites. The improved electrical conductivity and dielectric properties make the ternary nanocomposites attractive in practical applications.     

Effect of various combinations of zirconia and organoclay nanoparticles on mechanical and thermal properties of an epoxy nanocomposite coating

An epoxy based nanocomposite coating containing various combinations of treated-zirconia and clay nanoparticles were prepared. Morphology and dispersion of nanoparticles within the nanocomposites were evaluated using optical microscopy, XRD and TEM analyses. Mechanical, thermal properties and corrosion resistance of nanocomposites were studied using; tensile strength measurements, DMTA and DSC analyses and salt spray test.The results showed that simultaneous use of spherical and plate-shape nanoparticles, have a positive effect on the clay exfoliation behavior in resulting nanocomposites.Mechanical properties of nanocomposites containing nano-zirconia slightly increased compared with neat-epoxy coating. Mechanical properties of nanocomposites containing various wt.% of clay or ZrO₂/clay nanoparticles slightly decreased; formation of physical barrier clay stacks, which leads to disturbing curing procedure and decreasing polymer cross-linking density, and development of nano-sized voids in the trapped regions by clay stacks. Corrosion performance of nanocomposites increased with addition of nanoparticles, due to improving barrier properties of the coating.     

Synthesis and electrocatalytic activity of platinum nanoparticle/carbon nanotube composites

Pt/CNT nanocomposite materials with an average platinum particle size of 3–5 nm and platinum content of 13–28 wt % have been prepared by reducing chloroplatinic acid, H₂PtCl₆, in the presence of conical carbon nanotubes. The effect of synthesis conditions on the average platinum particle size, total platinum content, and surface composition of the nanocomposites has been studied using X-ray photoelectron spectroscopy, IR spectroscopy, electron microscopy, X-ray diffraction, and thermogravimetry. The materials have been tested as catalysts for hydrogen oxidation and oxygen reduction. Their performance has been assessed by cyclic and steady-state voltammetric techniques. The structure and composition effects on the electrocatalytic properties of the nanocomposites are discussed.     

Dispersion of functionalized multi-walled carbon nanotubes in multi-walled carbon nanotubes/liquid crystal nanocomposites and their thermal properties

A novel liquid crystal functionalized multi-walled carbon nanotubes (LC-MWNTs)/2-methyl-N,N′-bis(4′-methoxy benzoyloxy)-terephthalamide liquid crystal (LC) nanocomposite (LC-MWNTs/LC) was prepared via solution blend. The dispersion and thermal property of the nanocomposites with different loadings of LC-MWNTs (0.1-1 wt.%) were investigated using SEM, TGA and DSC. The results show that the dispersion of LC-MWNTs in LC matrix is more homogeneous than purified MWNTs. The decomposition temperature of nanocomposites exhibits obvious decrease at first and then increase with increasing concentration of LC-MWNTs, which is lower than that of LC for 0.1-0.4 wt.% LC-MWNT loadings and higher than that of LC for 0.5-1 wt.% LC-MWNT loadings. The addition of LC-MWNTs has little effects on the texture of smectic mesophase. These results illustrate the LC-MWNTs/LC nanocomposites, which have lower melting point and higher decomposition temperature than those of LC by adding adequate amount of LC-MWNTs, show a wide temperature range of mesophase and high thermostability. The increased mesophase temperature region of LC materials will be beneficial to their practical applications.     

Carbothermal transformation of a graphitic carbon nanofiber/silica aerogel composite to a SiC/silica nanocomposite

Carbon nanofiber/silica aerogel composites are prepared by sol-gel processing of surface-enhanced herringbone graphitic carbon nanofibers (GCNF) and Si(OMe)4, followed by supercritical CO2 drying. Heating the resulting GCNF/silica aerogel composites to 1650 degrees C under a partial pressure of Ar gas initiates carbothermal reaction between the silica aerogel matrix and the carbon nanofiber component to form SiC/silica nanocomposites. The SiC phase is present as nearly spherical nanoparticles, having an average diameter of ca. 8 nm. Formation of SiC is confirmed by powder XRD and by Raman spectroscopy.     

Studies on the photo-catalytic activity of semiconductor nanostructures and their gold core-shell on the photodegradation of malathion

This work is devoted to the synthesis of different semiconductor nanoparticles and their metal core-shell nanocomposites such as TiO2, Au/TiO2, ZnO, and Au/ZnO. The morphology and crystal structures of the developed nanomaterials were characterized by transmission electron microscopy (TEM) and x-ray diffraction (XRD). These materials were used as catalysts for the photodegradation of malathion, which is one of the most commonly used pesticides in developing countries. The degradation of 10 ppm malathion under ultraviolet (UV) and visible light in the presence of different synthesized nanocomposites was analyzed using high performance liquid chromatography (HPLC) and UV-visible spectra. A comprehensive study was carried out for the catalytic efficiency of the prepared nanoparticles. Moreover, the effects of different factors that could influence catalytic photodegradation, such as different light sources, surface coverage and the nature of the organic contaminants, were investigated. The results indicate that the core-shell nanocomposite of semiconductor-gold serves as a better catalytic system than the semiconductor nanoparticles themselves.     

Chemical fluid deposition of monometallic and bimetallic nanoparticles on ordered mesoporous silica as hydrogenation catalysts

A simple and green method of depositing monometallic (Ru, Rh, Pd) and bimetallic nanoparticles (Ru-Rh, Ru-Pd and Rh-Pd) on an ordered mesoporous silica support (MCM-41) in supercritical carbon dioxide (scCO2) is described. Metal acetylacetonates were used in the experiments as CO2-soluble metal precursors. Suitable temperature and pressure conditions for synthesizing each kind of nanoparticles were applied in this study. The characterizations of these nanocomposites were performed by transmission electron microscopy (TEM), X-ray diffraction (XRD) and energy dispersive X-ray spectroscopy (EDS). The nanoparticles had average sizes varying from 2 nm to 8 nm. The Ru nanoparticles were clearly shown to be inside the mesopores of MCM-41 from the TEM image. These nanocomposites used as catalysts for hydrogenation was demonstrated. The efficiency of the scCO2 prepared Ru/MCM-41 catalyst was nearly 8 times than that of a Ru/MCM-41 catalyst prepared by conventional impregnation method.     

树脂基Fe纳米粒子及碳纤维复合吸波平板的制备与性能

以Fe纳米粒子(Fe NPs)为吸波剂,偶联剂KH550为表面改性剂,碳纤维(CFs)作为增强及电磁波反射相,环氧树脂(ER)作为基体,制备多种吸波平板并对其综合性能及相关机制进行研究。结果表明:平板的吸波性能随Fe NPs和CFs含量的增加而提高,吸收剂浓度梯度分布有助于形成特定频段的共振吸收;平板对电磁波损耗具有明显的各向异性,表现为CFs垂直电磁波入射方向时性能优于平行情况,当Fe NPs的含量为30%(质量分数,下同),CFs为5.52%,板厚为4.56mm时,最小反射损耗为-26.8dB(4.9GHz);同时,CFs可改善平板的抗弯性能,当Fe NPs为30%时,弯曲强度相比于纯树脂时仅降低了5.81%。     

TiN-Al2O3纳米复合材料的力学性能和导电性能

以纳米TiN和α-Al₂O₃粉体为原料,采用球磨混合法制备了纳米TiN-Al₂O₃复合粉体,通过热压烧结得到致密烧结体.研究了纳米TiN颗粒对Al₂O₃材料力学性能和导电性能的影响,实验结果表明:在Al₂O₃基体中加入15vol％TiN纳米颗粒时,Al₂O₃材料的弯曲强度和断裂韧性分别从370MPa和3.4MPa·m^1/2提高到690MPa和5.1MPa·m^1/2,随着TiN添加量的增加,复合材料的电阻率逐渐降低,在25vol％TiN时达到最低值(6.5×10^-3Ω·cm).     

Effects of modified and non-modified clay on the rheological behavior of high density polyethylene

HDPE nanocomposites containing 2.5, 5 and 10 wt.% of non-modified and modified clays (NMC and MC) were prepared by melt extrusion in a twin screw extruder. Compression molded samples were prepared. Transmission electron microscopy (TEM) indicated a partial intercalation of the modified clay nanofiller within the HDPE matrix comparing to that of non-modified clay. The moduli of nanocomposites increased with increase in nanofiller concentration; but this increase was greater in the low frequency region. The non-modified clay had a greater increase in the elastic behavior, while the modified clay increased viscose behavior because of more interactions with the matrix and partial intercalation. The rheological behaviors of both HDPE/NMC and HDPE/MC nanocomposites are more sensitive to nanoparticles’ concentration at low frequencies. The HDPE/MC nanocomposites showed semi-circle shapes comparing to HDPE/NMC nanocomposites. While the Cole–Cole plot of HDPE/NMC nanocomposite had more departure of semi-circle shape. The agglomerated particles could concentrate the imposed stress so the yield stress reached at lower shear rates comparing to pure HDPE and HDPE filled 2.5 wt.% NMC nanocomposite. Study of suspension models showed that the Eilers-Van Dijck and Einsten models fitted to almost experimental data satisfactorily.     

Synthesis of core/shell spinel ferrite/carbon nanoparticles with enhanced cycling stability for lithium ion battery anodes

Monodispersed core/shell spinel ferrite/carbon nanoparticles are formed by thermolysis of metal (Fe3+, Co2+) oleates followed by carbon coating. The phase and morphology of nanoparticles are characterized by x-ray diffraction and transmission electron microscopy. Pure Fe3O4 and CoFe2O4 nanoparticles are initially prepared through thermal decomposition of metal–oleate precursors at 310 degrees C and they are found to exhibit poor electrochemical performance because of the easy aggregation of nanoparticles and the resulting increase in the interparticle contact resistance. In contrast, uniform carbon coating of Fe3O4 and CoFe2O4 nanoparticles by low-temperature (180 degrees C) decomposition of malic acid allowed each nanoparticle to be electrically wired to a current collector through a conducting percolative path. Core/shell Fe3O4/C and CoFe2O4/C nanocomposite electrodes show a high specific capacity that can exceed 700 mAh g(-1) after 200 cycles, along with enhanced cycling stability.     

Effect of highly dispersible zirconia nanoparticles on the properties of UV-curable poly(urethane-acrylate) coatings

Highly crystalline and dispersible zirconia nanoparticles, ex situ synthesized from a solvothermal reaction of zirconium(IV) isopropoxide isopropanol complex in benzyl alcohol, were functionalized with 3-(trimethoxysilyl)propyl methacrylate and blended with UV-curable urethane-acrylate formulations to fabricate poly(urethane-acrylate)/zirconia (PUA/ZrO₂) nanocomposite coatings. A critical ZrO₂ concentration of 20 wt% was observed for the evolutions of both the structure and properties of the nanocomposites as a function of ZrO₂ content. Below the critical concentration, completely transparent nanocomposite film was obtained and the nanocomposites exhibited increasing final carbon–carbon double bond conversion, refractive index, hardness, elastic modulus, and thermal stability as ZrO₂ content increased. However, serious agglomeration of ZrO₂ nanoparticles occurred at 25 wt% of ZrO₂, which decreased final conversion, transparency and hardness, and thermal stability of the nanocomposite film. These results clearly reveal that the performance of UV-curable nanocomposites is strongly dependent on the dispersion of nanoparticles.     

Facile synthesis of carbon supported copper nanoparticles from alginate precursor with controlled metal content and catalytic NO reduction properties

A copper-nanoparticle-doped carbon was prepared from an alginate based precursor in a one step carbonisation-reduction procedure based on the modified polyol process. The ion exchange capacity of the precursor as well as the porosity, metal content, thermal properties, of the final product, were investigated. The preparation route leads to a porous carbon/copper composite with predefined metal loading reaching up to over 30% (w/w) of finely dispersed Cu nanoparticles of fairly uniform size. NO catalytic abatement evaluation showed high efficiency even at low temperatures compared to other recently reported carbon supported catalysts.     

Synthesis and characterization of dual particle (MWCT+B4C) reinforced sintered hybrid aluminum matrix composites

ABSTRACT

Metal matrix nanocomposites (MMNCs) consist of a metal matrix reinforced with nanoparticles, featuring physical and mechanical properties very different from those of the matrix. Especially carbon nanotubes (CNTs) can improve the matrix material in terms of wear resistance, damping properties, and mechanical strength. The present investigation deals with the synthesis and characterization of aluminum matrix reinforced with micro-B₄C particles, and multiwall carbon nanotubes (MWCNTs) which have been prepared by powder metallurgy route. Powder mixture containing fixed weight (%) of B₄C and different wt% of MWCNT as reinforcement constituents that are uniaxial cold pressed and later green compacts are sintered in continues electric furnace. Microstructure and Mechanical properties such as microhardness and density are examined. Microstructure of samples has been investigated using scanning electron microscope (SEM). X-ray diffraction(XRD), energy dispersive x-ray (EDAX), atomic force microscope (AFM), and transmission electron microscope (TEM). TEM microstructure of the nanocomposite shows the homogeneous dispersion of MWCNT in the aluminum matrix. The results indicated that the increase in wt % of MWCNT improves the bonding and mechanical properties.     

Synthesis and characterization of PtRe alloy nanoparticles as electrocatalysts for methanol oxidation

We report a new synthesis of PtRe alloy nanoparticles (NPs) and their electrocatalytic activity for methanol oxidation. PtRe alloy NPs with controlled composition were prepared by a capping agents-based colloidal method. In the synthesis, trioctylamine was used as high-boiling solvent, and oleylamine/oleic acid were employed as capping agents to control the particle size and dispersion. The PtRe NPs were fully characterized by TEM, EDX, XRD and XPS. The as-prepared PtRe NPs had a narrow size distribution, and displayed a good dispersion in hydrocarbon solvents. Carbon-supported PtRe catalysts were prepared by physical deposition of as-prepared particles on carbon powder, followed by the catalytic activation at 400 degrees C in Ar/H2. Electrochemical studies showed the PtRe catalysts had high activity for methanol electrooxidation.     

Influence of metal nanoparticle decorated CNTs on polyurethane based electro active shape memory nanocomposite actuators

Polymer nanocomposites based on thermoplastic polyurethane (PU) elastomer and metal nanoparticle (Ag and Cu) decorated multiwall carbon nanotubes (M-CNTs) were prepared through melt mixing process and investigated for its mechanical, dynamic mechanical and electro active shape memory properties. Structural characterization and morphological characterization of the PU nanocomposites were done using X-ray diffraction (XRD) and scanning electron microscopy (SEM). Morphological characterization revealed better dispersion of M-CNTs in the polyurethane, which is attributed to the improved interaction between the M-CNTs and polyurethane. Loading of the metal nanoparticle coated carbon nanotubes resulted in the significant improvement on the mechanical properties such as tensile strength of the PU composites in comparison to the pristine carbon nanotubes (P-CNTs). Dynamic mechanical analysis showed that the glass transition temperature (Tg) of the polyurethane increases slightly with increasing loading of both pristine and metal nanoparticle functionalized carbon nanotubes. The metal nanoparticles decorated carbon nanotubes also showed significant improvement in the thermal and electrical conductivity of the PU/M-CNTs nanocomposites. Shape memory studies of the PU/M-CNTs nanocomposites exhibit remarkable recoverability of its shape at lower applied dc voltages.