Conducting polymer coated graphene oxide reinforced C–epoxy composites for enhanced electrical conduction

Enhanced electrical conductivities were achieved in C–epoxy composites by integrating them with conducting polymers (CPs), namely poly pyrrole (PPY), poly(3,4-ethylene dioxythiophene) (PEDOT) and graphene oxide (GO) enwrapped by CPs. By in-situ polymerization of pyrrole or 3,4-ethylenedioxythiophene (EDOT) in the presence of the GO (template), sodium bis(2-ethylhexyl) sulfosuccinate (structure directing agent), ferric chloride (oxidant), the electrically conductive sheets of GO enwrapped CPs were obtained. The formation of CP coating on GO was confirmed by Raman spectroscopy, scanning electron microscopy and thermo gravimetric analysis studies. Different wt% of CP and CP coated GO were added to the epoxy resin and this resin was used to prepare the 2D laminated C–epoxy composites by hand layup method. DC electrical conductivity of the prepared C–epoxy composites were analyzed using current–voltage (I–V) characteristics and impedance measurements. Typical results showed that CP coated GO, at 0.5 wt% addition to epoxy imparted highest DC electrical conductivity for C–epoxy composite.     

Reaction synthesis of TiC–TiB<Subscript>2</Subscript>/Al composites from an Al–Ti–B<Subscript>4</Subscript>C system

The TiC–TiB₂/Al composites were fabricated by self-propagating high-temperature synthesis (SHS) from Al–Ti–B₄C compacts. The addition of Al to the Ti–B₄C reactants facilitates the ignition occurrence, lowers the reaction exothermicity, and modifies the resultant microstructure. The maximum combustion temperature and combustion wave velocity decrease with the increase in the Al amount. The B₄C particle size exerts a significant effect on the combustion wave velocity and the extent of the reaction, while that of Ti has only a limited influence. The reaction products are primarily dependent on the B₄C particle size and the Al content in the reactants. Desired products consisting of only the TiC, TiB₂, and Al phases could be obtained by a cooperative control of the B₄C particle size and the Al content.     

Graphene/TiO<Subscript>2</Subscript> hydrogel: a potential catalyst to hydrogen evolution reaction

In this study, graphene was synthesized from graphite. Graphite was oxidized via modified Hummer’s method and sonicated to form graphene oxide (GO). Infrared spectroscopy revealed the successful oxidation of graphite by the emergence of oxygen functionalities. The spectrum of GO showed peaks at 3270, 1629, 1227 and 1096 cm^?1, indicating O–H, C=O, C–OH and C–O–C functional groups, respectively. Graphene hydrogels were prepared by the addition of L-ascorbic acid to GO suspensions and subsequent heating at 90^°C. Composite hydrogels of graphene and titanium (IV) oxide (TiO₂) were synthesized with various TiO₂ to GO mass ratios. Composites were applied to photocatalytic hydrogen evolution reaction (HER) and the hydrogen gas produced was analysed by gas chromatography with thermal conductivity detector. Highest HER yield was 66.00% H₂.     

Surface charge induced tuning of electrical properties of CVD assisted graphene and functionalized graphene sheets

We demonstrate a new approach to tune the electrical properties of graphene and functionalized graphene. Graphene was synthesized using thermal chemical vapour deposition(TCVD) method on copper foil using precursor gas acetylene and co-catalyst H2 gas. TCVD assisted graphene was successfully transferred onto a silicon wafer. Transferred graphene sheet was then functionalized to prepare graphene oxide(GO) and reduced graphene oxide(rGO). Different surface charge carbon nanoparticles, e.g. carbon nanoparticle with net positive charge and carbon nanoparticle with net negative charge were then immobilized on transferred graphene and functionalized graphene sheets. The functionalized graphene and charge mobilized functionalized graphene were characterized by Uv–vis spectroscopy,Fourier transformed infrared spectroscopy, scanning electron microscopy, and Raman spectroscopy. After immobilization of carbon nanomaterials, the ac electrical conductivity was found to increase due to enhancement of the surface charge, electron density, and mobility. It was observed that negative surface charge immobilized graphene and functionalized graphene show higher conductivity. Thus, the electrical property of graphene and functionalized graphene can be tuned by surface modification with different surface charge carbon nanomaterials.     

Reinforcing graphene oxide/cement composite with NH<Subscript>2</Subscript> functionalizing group

In this study, pure and NH₂-functionalized graphene oxide (GO) nanosheets have been added to the cement mortar with different weight percents (0.05, 0.10, 0.15, 0.20 and 0.25 wt%). In addition, the effects of functionalizing GO on the microstructure and mechanical properties (flexural/compressive strengths) of cement composite have been investigated for the first time. Scanning electron microscopy (SEM) images showed that GO filled the pores and well dispersed in concrete matrix, whereas exceeding GO additive from 0.10 wt% caused the formation of agglomerates and microcracks. In addition, mercury intrusion porosimetry confirmed the significant effects of GO and functionalizing groups on filling the pores. NH₂-functionalizing helped to improve the cohesion between GO nanosheets and cement composite. Compressive strengths increased from 39 MPa for the sample without GO to 54.23 MPa for the cement composites containing 0.10 wt% of NH₂-functionalized GO. Moreover, the flexural strength increased to 23.4 and 38.4% by compositing the cement paste with 0.10 wt% of pure and NH₂-functionalized GO, compared to the sample without GO, respectively. It was shown that functionalizing considerably enhanced the mechanical properties of GO/cement composite due to the interfacial strength between calcium silicate hydrates (C-S-H) gel and functionalized GO nanosheets as observed in SEM images. The morphological results were in good agreement with the trend obtained in mechanical properties of GO/cement composites.     

TiO<Subscript>2</Subscript> nanocrystals grown on graphene as advanced photocatalytic hybrid materials

A graphene/TiO₂ nanocrystals hybrid has been successfully prepared by directly growing TiO₂ nanocrystals on graphene oxide (GO) sheets. The direct growth of the nanocrystals on GO sheets was achieved by a two-step method, in which TiO₂ was first coated on GO sheets by hydrolysis and crystallized into anatase nanocrystals by hydrothermal treatment in the second step. Slow hydrolysis induced by the use of EtOH/H₂O mixed solvent and addition of H₂SO₄ facilitates the selective growth of TiO₂ on GO and suppresses growth of free TiO₂ in solution. The method offers easy access to the GO/TiO₂ nanocrystals hybrid with a uniform coating and strong interactions between TiO₂ and the underlying GO sheets. The strong coupling gives advanced hybrid materials with various applications including photocatalysis. The prepared graphene/TiO₂ nanocrystals hybrid has superior photocatalytic activity to other TiO₂ materials in the degradation of rhodamine B, showing an impressive three-fold photocatalytic enhancement over P25. It is expected that the hybrid material could also be promising for various other applications including lithium ion batteries, where strong electrical coupling to TiO₂ nanoparticles is essential.     

TiO<Subscript>2</Subscript>/graphene composite from thermal reaction of graphene oxide and its photocatalytic activity in visible light

In this study, the P25 TiO₂ nanoparticles and graphene sheets (GSs) composite were prepared from a facile thermal reaction of graphene oxide. Its microstructures and photocatalytic properties were characterized and measured using X-ray diffraction (XRD), high resolution transmission electron microscopy (HRTEM), Brunauer–Emmett–Teller (BET) specific area analysis, X-ray photoelectron spectroscopy (XPS), FT-IR spectra, and ultraviolet–visible (UV–vis) diffuse reflectance spectroscopy. Compared with pure P25 nanoparticles, the results reveal that (1) there is a red shift about 20 nm in the absorption edge of the P25/graphene composite; (2) the photocurrent of the composite is about 15 times higher than that of pure P25; (3) the visible light photocatalytic activity of the composite is enhanced greatly on decomposition of methylene blue (MB). The photocatalytic mechanism of the P25/graphene composite is also discussed.     

Effect of mechanical milling on the corrosion behavior of Al–Zn/Al<Subscript>2</Subscript>O<Subscript>3</Subscript> composite in NaCl solution

Ceramic particle reinforced aluminum metal matrix composites (MMCs) have resulted in potential use in aerospace and automobile industries. The composites have been processed by mechanical milling followed by traditional powder metallurgy route. The Al crystallite size is reduced to 27 nm after 60 h of milling. Results of the corrosion tests, evaluated using the potentiodynamic method in the NaCl solution, indicate that corrosion of the investigated composite materials depends on the weight fraction of the reinforcing particles. It has been found out, based on the determined anode polarization curves, that the investigated materials are susceptible to pitting corrosion. Moreover, experimental results suggest that the milled composite material Al–Zn/Al₂O_3p has higher corrosion resistance in the selected environment compared to unmilled composite Al–Zn/Al₂O_3p. Polarization curves show that the milling procedure improves the composite corrosion resistance in passive conditions. This is illustrated by the corrosion potential, which becomes nobler with milling.     

Enhanced thermal conductivity and retained electrical insulation for polyimide composites with SiC nanowires grown on graphene hybrid fillers

Polyimide (PI) composites containing one-dimensional SiC nanowires grown on two-dimensional graphene sheets (1D–2D SiC_NWs-GSs) hybrid fillers were successfully prepared. The PI/SiC_NWs-GSs composites synchronously exhibited high thermal conductivity and retained electrical insulation. Moreover, the heat conducting properties of PI/SiC_NWs-GSs films present well reproducibility within the temperature range from 25 to 175 °C. The maximum value of thermal conductivity of PI composite is 0.577 W/mK with 7 wt% fillers loading, increased by 138% in comparison with that of the neat PI. The 1D SiC nanowires grown on the GSs surface prevent the GSs contacting with each other in the PI matrix to retain electrical insulation of PI composites. In addition, the storage modulus and Young’s modulus of PI composites are remarkably improved in comparison with that of the neat PI.     

Relationship between thermal and sliding wear behavior of Al6061/Al<Subscript>2</Subscript>O<Subscript>3</Subscript> metal matrix composites

Al6061 alloy and Al6061/Al₂O₃ metal matrix composites (MMCs) were fabricated by stir casting. The MMCs were prepared by addition of 5, 10 and 15 wt% Al₂O₃ particulates and the size of particulates was taken as 16 μm. The effect of Al₂O₃ particulate content, thermal properties and stir casting parameters on the dry sliding wear resistance of MMCs were investigated under 50–350 N loads. The dry sliding wear tests were performed to investigate the wear behavior of MMCs against a steel counterface (DIN 5401) in a block-on-ring apparatus. The wear tests were carried out in an incremental manner, i.e., 300 m per increment and 3,000 m in total. It was observed that, the increase in Al₂O₃ vol% decreased both thermal conductivity and friction coefficient and hence increased the transition load and transition temperature for mild to severe wear during dry sliding wear test.     

Oxidation behavior and electrochemical corrosion performance of Ti<Subscript>3</Subscript>Al alloy with TiAl coating

Magnetron-sputter deposition was used to produce a Ti–48Al–8Cr–2Ag (at. %) coating on a Ti–24Al– 17Nb–0.5Mo (at. %) alloy substrate. Oxidation behavior was studied in air at 900–1000°C. The results indicated that the oxidation rate of sputtered Ti–48Al–8Cr–2Ag nanocrystalline coating was lower than that of the Ti₃Al alloy at 900°C. The former formed a scale of merely Al₂O₃, and the latter formed a scale of TiO₂. However, the Ti–48Al–8Cr–2Ag nanocrystalline coating showed a little bit higher oxidation rate than Ti₃Al alloy at 1000°C because the outer TiO₂ scale formed and columnar boundaries of the coating gave a larger actual oxidation area than the original alloy. The electrochemical corrosion behavior was investigated in a 3.5% NaCl solution at room temperature. The coating showed excellent electrochemical corrosion resistance in 3.5% NaCl solution because it exhibited stable passive polarization behavior without any overpassivation phenomena.     

Synthesis of carbon nanotube,graphene, CoFe<Subscript>2</Subscript>O<Subscript>4</Subscript>, and NiFe<Subscript>2</Subscript>O<Subscript>4</Subscript> polypyrrole nanocomposites and study their microwave absorption

In this experimental work, different conductive polymer nanocomposites were synthesized using polypyrrole as conductive polymer and CoFe₂O₄, NiFe₂O₄, CNT and graphene as fillers. X-ray diffraction pattern was used to study the crystallinity of the products and it was found CoFe₂O₄, NiFe₂O₄, CNT, and graphene were successfully embedded in the polymer matrix. To further approve the synthesis of the nanocomposites, energy dispersive X-ray spectroscopy was served. Surface groups of the synthesized nanocomposites were studied by Fourier transform infrared and Raman spectroscopy. The morphology of the products was examined by scanning electron microscopy and transmission electron microscopy. It was found the fillers were successfully embedded in the polymer matrix and they were in nanometer scales. To investigate the magnetic properties and conductivity of the polymer nanocomposites, alternating gradient force magnetometer and four-point probe were used, respectively. Finally, the microwave absorption properties of the polymer nanocomposites were studied and it was found the fillers have different effects on the polymer microwave absorption value.     

The effect of interfacial state on the thermal conductivity of functionalized Al2O3 filled glass fibers reinforced polymer composites

Rapidly increasing packaging density of electronic devices puts forward higher requirements for thermal conductivity of glass fibers reinforced polymer (GFRP) composites, which are commonly used as substrates in printed circuit board. Interface between fillers and polymer matrix has long been playing an important role in affecting thermal conductivity. In this paper, the effect of interfacial state on the thermal conductivity of functionalized Al₂O₃ filled GFRP composites was evaluated. The results indicated that amino groups-Al₂O₃ was demonstrated to be effective filler to fabricate thermally conductive GFPR composite (1.07 W/m K), compared with epoxy group and graphene oxide functionalized Al₂O₃. It was determined that the strong adhesion at the interface and homogeneous dispersion of filler particles were the key factors. Moreover, the effect of interfacial state on dielectric and thermomechanical properties of GFRP composites was also discussed. This research provides an efficient way to develop high-performance GFRP composites with high thermal conductivity for integrated circuit packaging applications.     

Carbon black/graphite nanoplatelet/rubbery epoxy hybrid composites for thermal interface applications

Hybrid composites were developed by dispersing carbon black (CB) nanoparticles and graphite nanoplatelets (GNPs) at 4–6 and 12–14 wt%, respectively, into rubbery epoxy resin. SEM analysis showed that CB particles improved the dispersion of GNPs in the hybrid composite. The thermal conductivity of 4 wt% CB/14 wt% GNP-15/rubbery epoxy hybrid composite, 0.81 W/m K, is ca. four times higher than that of rubbery epoxy. When silane-functionalised, the fillers reduced the viscosity of the hybrid dispersion and made the hybrid composite highly electrically insulating. Nevertheless, filler functionalisation decreased the composite’s thermal conductivity by only 16.6%. Compression testing showed that the hybrid fillers increased the compressive modulus and strength of rubbery epoxy by nearly two and three times, respectively. Overall, the hybrid composites with their thermal paste-type morphology, low viscosity, high compliance, improved thermal conductivity and, when fillers are functionalised, low electrical conductivity makes them promising materials as thermal interface adhesives.     

Properties of synthetic diamond and graphene nanoplatelet-filled epoxy thin film composites for electronic applications

Epoxy thin film composites filled with particulate nanofillers; synthetic diamond and graphene nanoplatelets were prepared and characterized based on tensile, thermal, and electrical properties. The influences of these two types of fillers, especially in terms of their loading, sizes and shapes, were discussed. It was found that the epoxy thin film composites incorporating synthetic diamond displayed optimum properties where the addition of synthetic diamond from 0 to 2 vol.% results in higher elastic modulus, tensile strength, elongation at break, thermal conductivity and storage modulus if compared to those of graphene nanoplatelets composites. Both thin film composites showed improvement in the glass transition temperature with increasing filler loadings. Results on the electrical conductivity of both systems showed that higher conductivity is observed in graphene nanoplatelets composites if compared to synthetic diamond composites.     

Effect of mechanical activation of Al(OH)<Subscript>3</Subscript> on its reaction with Li<Subscript>2</Subscript>CO<Subscript>3</Subscript>

The effect of preliminary mechanical activation of Al(OH)₃ on its solid-state reaction with Li₂CO₃ at temperatures above 800°C has been studied by thermogravimetry, X-ray diffraction, in situ X-ray diffraction, electron microscopy, and specific surface area and particle size measurements. The results demonstrate that preliminary mechanical activation of Al(OH)₃ in an AGO-2 planetary mill at 40g for 1 min allows phase-pure γ-LiAlO₂ to be obtained. The composition of the lithium aluminates resulting from mechanical activation and heat treatment depends on the phase composition of the aluminum oxides resulting from the thermal decomposition of Al(OH)₃. The particle size and specific surface area of the forming γ-LiAlO₂ have been determined.     

Laterally confined graphene nanosheets and graphene/SnO<Subscript>2</Subscript> composites as high-rate anode materials for lithium-ion batteries

High-rate anode materials for lithium-ion batteries are desirable for applications that require high power density. We demonstrate the advantageous rate capability of few-layered graphene nanosheets, with widths of 100–200 nm, over micro-scale graphene nanosheets. Possible reasons for the better performance of the former include their smaller size and better conductivity than the latter. Combination of SnO₂ nanoparticles with graphene was used to further improve the gravimetric capacities of the electrode at high charge-discharge rates. Furthermore, the volumetric capacity of the composites was substantially enhanced compared to pristine graphene due to the higher density of the composites.     

Wear behavior of TiB<Subscript>2</Subscript> inoculated 20Cr–3Mo–4C high chromium white cast irons

FeTi, B₂O₃, Al, and FeW particulates, approximately 40–60 μm in size, were mixed in stoichiometric ratio and sintered at 1,200 °C. The sintered particulates were added as 5 wt% to molten high chromium white cast iron over 50 C-deg above the melting temperature, and stirred at 1,000 rpm. The samples were investigated in three groups: (1) high Cr white cast iron inoculated by the particulates sintered from Al–FeTi–B₂O₃ particulates; (2) high Cr white cast iron inoculated by the sintered particulates derived from Al–FeTi, B₂O₃, and FeW particulates; and (3) specimens of the second group that were subsequently homogenized. The microhardness of ceramic particulates was measured as 2,800–3,400 HV₁₀. The effect of sintered particulate volume fraction on the abrasive wear resistance of the high chromium white cast iron was determined. The wear resistance and hardness of the composites improved significantly as a result of particulate inoculation. The application of the homogenization heat treatment to the inoculated samples produced a microstructure having homogeneously distributed particulates.     

Synthesis of In(OH)<Subscript>3</Subscript> and In<Subscript>2</Subscript>O<Subscript>3</Subscript> nanomaterials incorporating Au

In(OH)₃ and In₂O₃ nanocrystals of rectangular shape and incorporating Au were synthesized with a hydrothermal process and thermal decomposition. Powder X-ray diffraction, electron microscopy (SEM, TEM), and energy-dispersive spectroscopy studies reveal that elemental Au nanoparticles are dispersed on the surface of In(OH)₃ rectangular nanocrystals and incorporated into In₂O₃ nanoporous particles. UV–vis spectral measurements reveal a surface-enchanced plasma band near λ ~532 nm for both Au-incorporating nanomaterials. The BET surface areas of Au-incorporating In(OH)₃ and In₂O₃ are 26.2 and 35.5 m²/g, respectively. The incorporation of elemental Au in In(OH)₃ and In₂O₃ nanomaterials is attractive for sensor, catalyst and solar-cell applications.     

Effects of sodium oleate on synthesis and photocatalytic activity of Bi<Subscript>2</Subscript>WO<Subscript>6</Subscript>/Bi<Subscript>2</Subscript>O<Subscript>3</Subscript>@RGO

In this study, the effects of sodium oleate on synthesis of Bi₂WO₆/Bi₂O₃ loaded reduced graphene oxide photocatalyst was studied. The as-prepared composites were characterized by X-ray diffraction, Fourier transform infrared, X-ray photoelectron spectroscopy, UV–visible diffuse reflectance and photoluminescence spectroscopy. The results suggested that addition of sodium oleate not only promoted synthesis of Bi₂O₃, but also enhanced the reduction of GO to graphene. When the amount of sodium oleate was 4 mol (Bi:SO?=?1:1), Bi₂WO₆/Bi₂O₃@RGO to the best visible-light photocatalytic activity can be synthesized by a facile one-step solvothermal process without further reduction reaction. Hence, it indicated that sodium oleate could affect the synthesis of the as-prepared composites and the photocatalytic activity for degradation of RhB. This study did provide not only a facile method to synthesize Bi₂WO₆/Bi₂O₃@RGO, but also a method to reduce graphene oxide to graphene.