Characterization and temperature-dependent conductivity of polyaniline nanocomposites encapsulating gold nanoparticles on the surface of carboxymethyl cellulose

Polyaniline nanocomposites encapsulating gold nanoparticles on carboxymethyl cellulose surface were prepared via the polymerization of aniline hydrochloride with different carboxymethyl cellulose (CMC) concentrations (wt.%) using HAuCl₄ as oxidant. The synthesized composites were characterized by Fourier transform infrared (FTIR) spectroscopy. Surface morphology was studied by electron diffraction scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The embedded crystallinity of the composites was investigated by X-ray diffraction (XRD) analyses. The electrical property of the composites was examined by temperature-dependent DC conductivity in the range of 300–500 K. The composites exhibited higher electrical conductivities with increased CMC concentration under equivalent conditions. Activation energy for electron transport was also calculated based on the conductivity data.     

Synthesis of polyaniline-gold/graphene oxide composite and microwave absorption characteristics of the composite films

This paper describes the synthesis of polyaniline-gold nanocomposite by an in situ polymerization of aniline hydrochloride with graphene oxide using hydrogen tetrachloroaurate as an oxidant. The synthesized nanocomposites were characterized by FT-IR and UV–vis spectroscopy, and their surface morphology was studied by scanning and transmission electron microscopy. Microwave absorption property of the composite films was studied at 2–12 GHz, and the effects of sample thickness on the microwave absorption were investigated. The electromagnetic interference shielding effectiveness of PANI-GNP has been enhanced due to the inclusion of GO.     

Manufacturing techniques and property evaluations of conductive composite yarns coated with polypropylene and multi-walled carbon nanotubes

This study uses a melt extrusion method, a method for producing wires, to coat polyester (PET) yarns with polypropylene (PP) and multi-walled carbon nanotubes (MWCNTs). The resulting PP/MWCNTs-coated PET conductive yarns are tested for their tensile properties, processability, morphology, melting and crystallization behaviors, electrical conductivity, and applications. The test results indicate that tensile strength of the conductive yarns increases with an increase in the coiling speed that contributes to a more single-direction-orientated MWCNTs arrangement as well as a greater adhesion between PP/MWCNTs and PET yarns. 8 wt% MWCNTs results in an 18 °C higher crystallization temperature (T_c) of PP and an electrical conductivity of 0.8862 S/cm. The test results of this study have proven that this form of processing technology can prepare PP/MWCNTs-coated PET conductive yarns that have satisfactory tensile properties and electrical conductivity, and can be used in functional woven fabrics and knitted fabrics.     

Microstructure of carbon nanotubes/PET conductive composites fibers and their properties

Poly(ethylene terephthalate) (PET) resin has been compounded with carbon nanotubes (CNTs) using a twin-screw extruder. The composites of 4 wt% CNTs in PET had a volume electrical resistance of 10³ Ω cm, which was 12 orders lower than pure PET. The volume electrical conductivity of CNTs/PET composites with different CNTs containing followed a percolation scaling law of the form σ = κ(ρ − ρ_c)^t well. Scanning electron microscopy (SEM) micrograph showed that CNTs had been well dispersed in PET matrix. Optical microscopy micrograph showed that discontinuity of conductive phase existed in some segments of composite fiber. Rheological behavior of CNTs/PET composites showed that the viscosity of CNTs/PET composites containing high nanotube loadings exhibited a large decrease with increasing shear frequency. Crystallization behavior of CNTs/PET composites was studied by differential scanning calorimetry (DSC) and the nucleating effect of CNTs in the cooling crystallization process of PET was confirmed. Composite fiber was prepared using the conductive CNTs/PET composites and pure PET resin by composite spinning process. Furthermore, cloth was woven by the composite fiber and common terylene with the ratio 1:3. The cloth had excellent anti-static electricity property and its charge surface density was only 0.25 μC/m².     

Gold nanoparticle/single-walled carbon nanotube film on the surface of glassy carbon electrode and its application

A sensor based on gold nanoparticle/single-walled carbon nanotube film on the surface of glassy carbon electrode is prepared. Electrochemical behavior of adrenaline hydrochloride (AH) on the surface of gold nanoparticle/single-walled carbon nanotube modified glassy carbon electrode is investigated. A simple, sensitive, and inexpensive method for determination of AH is proposed. The oxidation peak currents is proportional to adrenaline hydrochloride concentrations in the range of 0.20 mg L^? 1 to 1.80 mg L^? 1 in 0.1 M phosphate buffer solution of pH 7.3, the detection limit for AH is 0.06 mg L^? 1, and the recoveries are in the range from 100.0 to 110.0% with RSD of 1.2–1.9% (n = 6).     

Synthesis of polypyrrole and carbon nano-fiber composite for the electrode of electrochemical capacitors

Nano-thin polypyrrole (PPy) films were deposited on vapor grown carbon fibers (VGCF) by using an in situ chemical polymerization of the monomer in the presence of FeCl₃ oxidant. An ultrasonic cavitational stream was used during polymerization of pyrrole, to enable the deposition of uniformly nano-thin PPy films on the surface of VGCF. The PPy/VGCF composite was characterized by FTIR spectroscopy. Surface morphology of the polymer films was characterized by using scanning electron microscopy and scanning transmission electron microscopy. The capacitance of the composite electrodes was investigated with cyclic voltammetry. As results of this study, thinner layer of PPy in the composite electrode (< 10 nm) was effective to obtain fully reversible and very fast Faradaic reaction. Hence, most mass of the PPy could contribute to the pseudo-capacitive charge storage. This nano-thin PPy layer exhibited higher specific capacitance of ∼588 F g^− 1 at 30 mV s^− 1 and ∼545 F g^− 1 at 200 mV s^− 1 along with an excellent power capability.     

PPy/graphene nanosheets/rare earth ions: A new composite electrode material for supercapacitor

Highly conductive PPy/graphene nanosheets/rare earth ions (PPy/GNS/RE³⁺) composites were prepared via in situ polymerization with p-toluenesulfonic acid as a dopant and FeCl₃ as an oxidant. The effects of GNS and RE³⁺ on the electrical conductivity of the composites were investigated. The results showed that the GNS as a filler had effect on the conductivity of PPy/GNS/RE³⁺ composites, which played an important role in forming a conducting network in PPy matrix. The microstructures of GNS and PPy/GNS/RE³⁺ were characterized by the SEM and TEM examinations. It was found that GNS and PPy nanospheres formed a uniform composite with the PPy nanospheres absorbed on the GNS surface and/or filled between the GNS. Such uniform structure together with the observed high conductivities afforded high specific capacitance when used as supercapacitor electrodes. A specific capacitance of as high as 238 F/g at a current density of 1 A/g was achieved over the PPy/GNS/Eu³⁺ composite.     

Three-dimensional graphene/polyaniline composite material for high-performance supercapacitor applications

A novel three-dimensional (3D) graphene/polyaniline nanocomposite material which is synthesized using in situ polymerization of aniline monomer on the graphene surface is reported as an electrode for supercapacitors. The morphology and structure of the material are characterized by scanning electron microscopy (SEM), transmission electron microscope (TEM), Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD). The electrochemical properties of the resulting materials are systematically studied using cyclic voltammetry (CV) and constant current charge–discharge tests. A high gravimetric capacitance of 463 F g^?1 at a scan rate of 1 mV s^?1 is obtained by means of CVs with 3 mol L^?1 KOH as the electrolyte. In addition, the composite material shows only 9.4% capacity loss after 500 cycles, indicating better cyclic stability for supercapacitor applications. The high specific surface area, large mesopore volume and three-dimensional nanoporous structure of 3D graphene could contribute to the high specific capacitance and good cyclic life.     

Silk fibroin immobilization on poly(ethylene terephthalate) films: Comparison of two surface modification methods and their effect on mesenchymal stem cells culture

Silk fibroin (SF) has played a curial role for the surface modification of conventional materials to improve the biocompatibility, and SF modified poly(ethylene terephthalate) (PET) materials have potential applications on tissue engineering such as artificial ligament, artificial vessel, artificial heart valve sewing cuffs dacron and surgical mesh engineering. In this work, SF was immobilized onto PET film via two different methods: 1) plasma pretreatment followed by SF dip coating (PET-SF) and 2) plasma-induce acrylic acid graft polymerization and subsequent covalent immobilization of SF on PET film (PET-PAA-SF). It could be found that plasma treatment provided higher surface roughness which was suitable for further SF dip coating, while grafted poly(acrylic acid) (PAA) promised the covalent bonding between SF and PAA. ATR-FTIR adsorption band at 3284 cm^? 1, 1623 cm^? 1 and 1520 cm^? 1 suggested the successful introduction of SF onto PET surface, while the amount of immobilized SF of PET-SF was higher than PET-PAA-SF according to XPS investigation (0.29 vs 0.23 for N/C ratio). Surface modified PET film was used as substrate for mesenchymal stem cells (MSCs) culture, the cells on PET-SF surface exhibited optimum density compared to PET-PAA-SF according to CCK-8 assays, which indicated that plasma pretreatment followed by SF dip coating was a simple and effective way to prepare biocompatible PET surface.     

A comparative study on low-velocity impact response of fabric composite laminates

Impact behaviors at low velocity of composite laminates reinforced with fabrics of different architectures are investigated. Unidirectional prepreg, 2D woven and 3D orthogonal fabrics, all formed of Ultrahigh Molecular Weight Polyethylene (UHMWPE) filaments, were selected as reinforcements to form composite laminates using hot pressing technology. Low velocity impact tests were conducted using a drop-weight impact equipment at the energy level of 35 J. A three-coordinate measuring device was employed to determine the volume of plastic deformation and surface dent diameter. The results show that the composite laminates of single-ply 3D orthogonal woven fabric exhibit better energy absorbed capacity and impact damage resistance as compared to those of unidirectional and 2D plain-woven fabric.     

Electrical thermal heating and piezoresistive characteristics of hybrid CuO–woven carbon fiber/vinyl ester composite laminates

The electric heating and piezoresistive characteristics of CuO–woven carbon fiber (CuO–WCF) composite laminates were experimentally evaluated. Hybrid CuO–WCF composites were fabricated via a two-step seed-mediated hydrothermal method. The interlaminar interface between two plies of hybrid CuO–WCF/vinyl ester composite laminae was influenced by interlocked fiber–fiber cross-linking structures with CuO NRs and acted as electric heating and resistance elements. The contribution of CuO NRs (10–110 mM) to the interlaminar interface was determined by measuring the temperature profile, in order to investigate the electrical resistive heating behavior. At higher concentration of CuO NRs growth in the interlaminar region applied by 3 A, the average temperature reached to 83.55 °C at the interface area 50 × 50 mm² and the heating efficiency was 0.133 W/°C owing to radiation and convection given by 10.5 W (3 A, 3.5 V). To investigate the piezoresistive response, the through-thickness gauge factor was observed at 0.312 during Joule heating applied by 2 A, compared with 0.639 at an ambient air temperature for CuO 110 mM concentration. The morphology and crystallinity of CuO NRs were investigated using scanning electron microscopy and X-ray diffraction analyses, respectively. The temperature dependence of hybrid CuO–WCF composite laminates’ storage moduli were analyzed using a dynamic mechanical analyzer. These characterizations showed that the interlaminar interface, combined with the high specific surface area of CuO NRs, provided the electron traps for electrical conduction around multiple WCF junctions and adjacent cross-linked laminae.     

Fabrication of conductive network formed by polyaniline-ZnO composite on fabric surfaces

A conductive network consisting of polyaniline (PANI) and PANI/nm-ZnO immobilized on the surfaces of poly(ethylene terephthalate) (PET) fabrics was synthesized by a route involving a wet-chemical technique and in-situ chemical oxidative polymerization procedures. Morphological, structural, thermal and electrical properties of the PET fabrics modified with PANI-ZnO composites were analyzed. X-ray diffraction (XRD) measurements of the composites revealed that the crystal structure of incorporated ZnO undergone a weak distortion during the polymerization reaction and the XRD pattern of PANI was predominate. Attenuated total reflection Fourier transform infrared spectroscopic studies indicated the presence of interaction between ZnO nanorods and molecular chains of PANI in the ZnO/PANI layers. Field emission scanning electron microscope images implied the thin composite layers showed a submicro-sized rod like network and the homogeneous distribution on the substrates. Thermogravimetric studies exhibited that the PET-ZnO/PANI composite had a higher thermal stability than anyone of PET and PET-PANI. The surface resistance of ZnO/PANI conductive films was found to be smaller than the PANI film, which was declined as aniline concentration in adsorption bath increased and reached a relatively low value when Zn(NO₃)₂ concentration was at 0.03 mol/L in the precursor solution.     

Preparation,morphology and properties of acid and amine modified multiwalled carbon nanotube/polyimide composite

The precursor of polyimide, polyamic acid, was prepared by reacting 4,4′-oxydianiline (ODA) with 3,3′,4,4′-benzophenone tetracarboxylic dianhydride (BTDA). Unmodified, acid-modified and amine-modified multiwall carbon nanotubes (MWCNT) were separately added to the polyamic acid and heated to 300 °C to produce polyimide/carbon nanotube composite. Scanning electron microscopic (SEM) and transmission electron microscopic (TEM) microphotographs reveal that acid-modified MWCNT and amine-modified MWCNT were dispersed uniformly in the polyimide matrix. The effect of the acid and amine-modified MWCNTs on the surface and volume electrical resistivities of MWCNT/polyimide composites were investigated . The surface electrical resistivity of the nanocomposites decreased from 1.28 × 10¹⁵ Ω/cm² (neat polyimide) to 7.59 × 10⁶ Ω/cm² (6.98 wt% unmodified MWCNT content). Adding MWCNTs influenced the glass transition temperatures of the nanocomposites. Modified MWCNTs significance enhanced the mechanical properties of the nanocomposites. The tensile strength of the MWCNT/polyimide composite was increased from 102 MPa (neat polyimide) 134 MPa (6.98 wt% acid modified MWCNT/polyimide composites).     

Effect of environment atmosphere on thermal shock resistance of the ZrB2–SiC–graphite composite

The thermal shock resistance of the ZrB₂–SiC–graphite composite was evaluated by measuring the retention of the flexural strength after the electrical resistance heating to the temperature ranging from 1000 °C up to 2500 °C. The experiment was operated in two different environment atmospheres (pure oxygen and low oxygen partial pressure which mixed O₂ and Ar with 1:9) at total pressure 2000 Pa. The residual strength for the specimen decreased gradually as the temperature increased up to 2200 °C, and it was slightly higher when heated in low oxygen partial pressure environment than in pure oxygen. In contrast to the specimen heated in low oxygen partial pressure environment, the residual strength for the specimen in pure oxygen increased steeply as the temperature increased from 1600 °C up to 1800 °C. The analysis of the SEM observations combined with EDS confirmed that the surface oxidation played a positive role in the thermal shock resistance of the ZrB₂–SiC–graphite composite with different environment atmospheres. The results here pointed out a potential method for charactering the effect of environment atmosphere on thermal shock resistance of the ZrB₂–SiC–graphite composite.     

Thermally induced porous carbon nanofibers for electrochemical capacitor electrodes from phenylsilane and polyacrylonitrile blend solutions

This work focuses on preparations of porous carbon composite nanofibers (CCNFs) with silicon-containing compounds and the introduction of a high specific surface area through the creation of pores by a simple thermal treatment. Blends of phenylsilane (PS) solutions at various concentrations and polyacrylonitrile (PAN) were electrospun into nanofibers. This process was followed by carbonization at 800 °C to create CCNFs with diameters of 60–200 nm and a high specific surface area of over 800 m²/g. The specific capacitance of the electrode in 6 M KOH solution was extraordinarily high (180 F/g).     

An investigation of contact resistance between carbon fiber/epoxy composite laminate and printed silver electrode for damage monitoring

An addressable conducting network (ACN) enables the structural condition to be monitored by the electrical resistance between electrodes on surface of CFRP (carbon fiber reinforced polymer) structure. To improve the reliability of ACN for damage detection, the contact resistance between the electrodes and CFRP laminates needs to be minimized. In this paper, the silver nanoparticles electrodes were fabricated via printed electronics techniques on CFRP composite. The contact resistance between the silver electrodes and CFRP was measured with respect to various fabrication conditions such as the sintering temperature of silver nanoink and the surface roughness of CFRP laminates. The interfaces between silver electrode and carbon fibers were observed using scanning electron microscope (SEM). From the study, it was found that the lowest contact resistance of 0.3664 Ω could be achieved when the sintering temperature of the silver nanoink and surface roughness were 120 °C and 230 nm, respectively.     

Superparamagnetic maghemite/polyrhodanine core/shell nanoparticles: Synthesis and characterization

Maghemite nanoparticles (MNPs) with a thin layer of polyrhodanine (PRd) at the surface were synthesized via chemical oxidative polymerization of rhodanine monomer at the MNPs surface in the presence of ferric chloride as oxidant. X-ray diffraction (XRD) pattern gave direct evidence that the synthesized nanoparticles are crystalline maghemite of about 8 nm in size. Magnetization of the particles versus an applied magnetic field exhibited no hysteresis loop, indicated superparamagnetic behavior in the particles. Transmission electron microscopy (TEM) together with Fourier-transform infrared (FT-IR) spectroscopy were used to determine the morphology and the chemical structure of the magnetic core and the polymeric shell. Through the microscopy analysis the shell thickness was estimated to be about 1.5 nm, whereas through thermogravimetric analysis (TGA) it was estimated to be about 0.6 nm. Moreover inductively coupled plasma optical emission spectroscopy (ICP-OES) measurements revealed that the oxidant residue in the polymer backbone is ca. 4 wt.%.     

Preparation and characterization of copper nanoparticles/zinc oxide composite modified electrode and its application to glucose sensing

We report a new method for selective detection of d(+)-glucose using a copper nanoparticles (Cu-NPs) attached zinc oxide (ZnO) film coated electrode. The ZnO and Cu-NPs were electrochemically deposited onto indium tin oxide (ITO) coated glass electrode and glassy carbon electrode (GCE) by layer-by-layer. In result, Cu-NPs/ZnO composite film topography was characterized by scanning electron microscopy (SEM) and atomic force microscopy (AFM), respectively. SEM and AFM confirmed the presence of nanometer sized Cu-NPs/ZnO composite particles on the electrode surface. In addition, X-ray diffraction pattern revealed that Cu-NPs and ZnO films were attached onto the electrode surface. Indeed, the Cu-NPs/ZnO composite modified electrode showed excellent electrocatalytic activity for glucose oxidation in alkaline (0.1 M NaOH) solution. Further, we utilized the Cu-NPs/ZnO composite modified electrode as an electrochemical sensor for detection of glucose. This glucose sensor showed a linear relationship in the range from 1 × 10^? 6 M to 1.53 × 10^? 3 M and the detection limit (S/N = 3) was found to be 2 × 10^? 7 M. The Cu-NPs/ZnO composite as a non-enzymatic glucose sensor presents a number of attractive features such as high sensitivity, stability, reproducibility, selectivity and fast response. The applicability of the proposed method to the determination of glucose in human urine samples was demonstrated with satisfactory results.     

Development of electromagnetic shielding materials from the conductive blends of polystyrene polyaniline-clay nanocomposite

Electromagnetic interference shielding composite materials were developed from the conductive blends of nanostructured polyaniline-clay composite (PANICN) and Polystyrene (PS) by a one step host matrix assisted emulsion polymerization of anilinium salt of 3-pentadecyl phenol-4-sulphonic acid (3-PDPSA) in clay. 3-PDPSA was derived from cashew nut shell liquid, a low cost renewable resource based product. These blends were characterized using Uv–visible and FT-IR spectroscopy, XRD, electrical conductivity, thermal property, dielectric property and electromagnetic shielding efficiency. The interactions between the primary particles and host matrix were elucidated from the studies made through spectroscopy and rheology. The key finding of the research is that this low cost PANICNPS blend with superior electrical conductivity (7.6 × 10^?1 S/m), excellent thermal stability and EMI SE of 10–20 dB at 8 GHz makes them as a promising candidate for application in EMI shielding and antistatic discharge matrix for the encapsulation of micro electronic devices.     

Influence of the molar concentration and substrate temperature on fluorine-doped zinc oxide thin films chemically sprayed

The effect of both the molar concentration of the starting solution and the substrate temperature on the electrical, morphological, structural and optical properties of chemically sprayed fluorine-doped zinc oxide (ZnO:F) thin films deposited on glass substrates is analyzed in this work. All the starting solutions employed were aged for 10 days before the deposition. The results show that as the molar concentration increases, a decrease in the electrical resistivity values is obtained, reaching the minimum resistivity in films ZnO:F deposited from a 0.4 M solution at 500 °C. A further increase in the molar concentration leads to a very slight increase in the resistivity. On the other hand, as the substrate temperature is increased, the resistivity decreases and a tendency towards to minimum value is evidenced; taking the molar concentration as parameter, minimum values are reached at 500 °C. The obtaining of ZnO:F thin films, with a resistivity as low as 7.8 × 10^− 3 Ω cm (sheet resistance of 130 Ω/□ and film thickness of 600 nm) measured in as-deposited films is reported here for the first time. The concurrent effect of the high molar concentration of the starting solution, the substrate temperature values used, and the ageing of the starting solution, which might cause polymerization of the zinc ions with the fluorine species, enhance the electrical properties. The structure of the films is polycrystalline, with a (002) preferential growth. Molar concentration rules the surface morphology as at low concentration an hexagonal and porous structure is developed changing to a uniform compact and small grain size surface in the films deposited with the high molar concentrations.