The thermal‐electrical properties of polyvinyl alcohol/AgNO3 films

In this article, one cast technique to fabricate 20–40 wt %AgNO₃‐doped polyvinyl alcohol (PVA) composite films of which electrical resistance sharply dropped (4–5 order) in a certain temperature range was reported. The phase, structure thermal, and electrical resistivity properties of films at different heat treatment temperatures were studied by X‐ray diffraction (XRD), scanning electrical microscopy (SEM) and differential scanning calorimetry (DSC). The results showed that all the AgNO₃ (20–40 wt %) doped PVA films presented an exothermic peak at 182°C. And the temperature of exothermic peak kept constant for various contents of AgNO₃. Meanwhile, the phase composition of the films was greatly affected by the heat treatment temperature. Ag particles were generated during the heat treatment process, and the content of Ag particles increased with increasing the temperature. The resistivity of PVA/AgNO₃ films decreased with increasing the temperature. And a sharp decrease appeared at 155–165°C due to the generation and contact of a mass of Ag particles at this temperature. The thermal‐electrical results suggested the applicability of these materials in temperature sensor, for example, critical temperature resistor thermistor. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Acidic hydrolysis of a poly(vinyl acetate) matrix by the catalytic effect of Ag nanoparticles and the micellization of Ag‐metal‐containing polymer

In this study, we conveniently obtained Ag(0)–polymer nanocomposites by reacting AgNO₃ with commercial poly(vinyl acetate) (PVAc) in the absence of a special reducing agent. The formation of Ag(0) metal was detected after formic acid (HCOOH) was added to a PVAc–AgNO₃ complex system, and some of the acetate groups of the PVAc backbone were hydrolyzed to form hydroxyl groups (OH) under the catalytic effect of the reduced Ag(O) metal. Here, the structure of the partially hydrolyzed PVAc backbone was represented as PVOH‐PVAc. X‐ray diffraction spectra showed that the Ag(0) metal generated in this method was in the form of Ag crystals. The structure of the Ag(0)–polymer was analyzed by ¹H‐NMR and ¹³C‐NMR spectroscopy. The micellization of the Ag(0)–polymer was also investigated by the addition of an inducing solvent to the formic acid solution of Ag(0)–polymer. The image showed that the morphology of the Ag micelles in the H₂O‐induced solvent was a Ag corona with a Ag shell, and that in the p‐xylene induced solvent showed a Ag cluster core structure. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 1457–1464, 2006     

Preparation and performance of a transparent poly(3,4‐ethylene dioxythiophene)–poly(p‐styrene sulfonate‐co‐acrylic acid sodium) film with a high stability and water resistance

Poly(p‐styrene sulfonate‐co‐acrylic acid sodium) (PSA) from the copolymerization of acrylic acid sodium and p‐styrene sulfonate monomers were used to dope poly(3,4‐ethylene dioxythiophene) (PEDOT) to generate PEDOT–PSA antistatic dispersions. Compared to those of the PEDOT–poly(p‐styrene sulfonate sodium) (PSS), the physical and electrical properties of the PEDOT–PSA conductive liquids were much better. The PEDOT–PSA films possessed a better water resistance without a decrease in the conductivity. The sheet resistance of the PEDOT–PSA–poly(ethylene terephthalate) (PET) films was about 1.5 × 10⁴ Ω/sq with a 100 nm thickness, the same as the PEDOT–PSS–PET films. The transmittance of the PEDOT–PSA–PET films exceeded 88%. Furthermore, the environmental dispersity of the PEDOT–PSA antistatic dispersion was apparently improved by the dopant PSA so that the stability was extraordinarily promoted. Meanwhile, the water resistances of the PEDOT–PSA–PET and PEDOT–PSA films were also enhanced. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45163.     

Electrical resistivity of polycarbonate/multiwalled carbon nanotube composites under varying injection molding conditions

Multiwalled carbon nanotube (MWCNT)‐filled polycarbonate composites were prepared by a corotating intermeshing twin‐screw extruder. The surface resistivities of compression‐ and injection‐molded specimens were quite different, the difference ranging from 10³ to 10⁷ Ω/sq at varying MWCNT concentrations. The surface resistivity of the injection‐molded specimen at 2 wt % loading varied up to 10⁵ Ω/sq in the specimen thickness direction and up 10⁴ Ω/sq in the polymer flow direction with respect to the gate. The difference in surface resistivity with the positions of injection‐molded specimen was confirmed with the morphology, which showed the difference in MWCNT number density (numbers/surface area). There was no significant effect on surface resistivity with injection pressure, holding pressure, and molding temperature. The specimens prepared at the injection speed of 13 mm/s showed surface resistivities 10³–10⁴ Ω/sq depending on the positions, which was comparable with the compression‐molded specimens, which had a surface resistivity of 10³ Ω/sq. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Using oxidation to increase the electrical conductivity of carbon nanotube electrodes

Recent studies have demonstrated that significantly low sheet resistance (Rs) (<100 Ω/sq; comparable to ITO) were achieved in single-walled carbon nanotube (SWCNT) films treated with HNO₃ followed by thionyl chloride. Here we show that H₂SO₄ can effectively reduce the Rs of SWCNT electrodes. H₂SO₄ treatment generates defects (COOH and SO₃H functionalities) on SWCNTs and the produced chemical functionalities are beneficial for enhancing the electrical conductivity in SWCNT electrodes. It is plausible that the H₂SO₄p-dopes the SWCNTs and the attachment of chemical functionalities helps to stabilize p-doping owing to their electron-deficient property.     

Fabrication of flexible transparent electrodes using PEDOT:PSS and application to resistive touch screen panels

The flexible transparent electrodes were fabricated by line patterning of conductive inks consisting of poly(3,4‐ethylenedioxythiophene) doped with poly(4‐styrenesulfonic acid) (PEDOT:PSS) water dispersion, ethylene glycol, isopropyl alcohol, and tetraethoxysilane (TEOS) on polyethylene terephthalate (PET) films. The values of sheet resistance (R_s), total light transmittance, haze, figure‐of‐merit, and pencil hardness of the PEDOT:PSS‐TEOS/PET film were found to be 301 Ω/sq., 85.0%, 2.4%, 41, and 2H, respectively. Furthermore, a resistive touch screen panel was fabricated using the PEDOT:PSS‐TEOS/PET film as the top electrode. It was found that the drawing on the resistive touch screen panel was successfully displayed on the PC screen with good in‐plane uniformity and maximum linearity of 0.8%. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45972.     

In vitro efficacy and toxicology evaluation of silver nanoparticle‐loaded gelatin hydrogel pads as antibacterial wound dressings

The silver nanoparticle (nAg)‐loaded gelatin hydrogel pads were prepared from 10 wt % gelatin aqueous solution containing silver nitrate (AgNO₃) at 0.75, 1.0, 1.5, 2.0, or 2.5 wt % by solvent‐casting technique. These AgNO₃‐containing gelatin solutions, that had been aged for 15, 12, 8, 8, and 8 h, respectively, showed noticeable amounts of the as‐formed nAgs, the size of which increased with an increase in the AgNO₃ concentration (i.e., from 7.7 to 10.8 nm, on average). The hydrogels were crosslinked with a glutaraldehyde aqueous solution (50 wt %, at 1 μL mL^?1). At 24 h of submersion in phosphate buffer saline (PBS) or simulated body fluid buffer (SBF) solution, about 40.5–56.4% or 44.4–79.6% of the as‐loaded amounts of silver was released. Based on the colony count method, these nAg‐loaded hydrogels were effective against Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa, with at least about 99.7% of bacterial growth inhibition. Unless they had been treated with a sodium metabisulfite aqueous solution, these hydrogels were proven, based on the indirect cytotoxicity evaluation, to be toxic to human's normal skin fibroblasts. Lastly, only the hydrogels that contained AgNO₃ at 0.75 and 1.0 wt % were not detrimental to the skin cells that had been cultured directly on them. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Highly transparent low resistance ATO/AgNWs/ATO flexible transparent conductive thin films

Indium-free flexible transparent conductive thin films (TCFs) composed of silver nanowire (AgNW) networks and Sb doped SnO₂ (ATO) layers were prepared on polyethylene terephthalate (PET) substrates. The ATO layers were deposited via radio frequency (RF) magnetron sputtering at room temperature. The AgNWs were achieved via a modified polyol reduction method and embedded between the ATO layers. The effects of AgNW networks and ATO layers on electrical and optical properties of the ATO/AgNWs/ATO flexible tri-layer thin films are investigated. The ATO layers can improve the optical transmittance and reduce the resistivity of tri-layers, and the corresponding mechanisms are proposed. Typically, an ATO/AgNWs/ATO flexible tri-layers show a high figure of merit value (30.06 × 10^-3 Ω^-1) with a low sheet resistance of 7.1 Ω/sq. and a high transmittance of 85.7%. Meanwhile, the tri-layers present excellent mechanical flexibility, and the ATO layers acted as the protecting layers improve the adhesive and environmental stability at high temperature and humidity for the ATO/AgNWs/ATO flexible tri-layers. These results indicate that ATO/AgNWs/ATO flexible tri-layer thin films can be useful for the fabrication of wearable electronic devices.     

Effect of NA-light radiation on the optical gap and crystal structure of AgNO3-diffused PVDF sensor

A casting method was used to prepare polyvinylidene fluoride (PVDF) and 1 wt % MnCl₂-filled PVDF films. AgNO₃ was allowed to diffuse through the filled films. The 3 types of the prepared films were irradiated by Na light with various doses. The post-irradiation and relaxation effects were investigated using ultraviolet–visible spectroscopy, X-ray analysis, and optical microscopy. The results were interpreted on the bases of a theoretical model previously suggested for a build-up and decay of radiation-induced conductivity associated with the transition of charge carriers in the presence of a uniform trap distribution. Various structures were proposed for the diffused AgNO₃ before and after irradiation. It was found that the induced change in optical gap, due to 5-min irradiation time for the AgNO₃ diffused films, exhibits no relaxation phenomenon. Accordingly, this film can be used in photorecording applications. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 70: 1759–1767, 1998     

Filling effect on the structural,electrical, and magnetic properties of PVAc/Co composites

Polyvinyl‐acetate/‐cobalt (PVAc/Co) composite films were prepared using a casting technique. The structural and physical properties were studied using X‐ray diffraction (XRD), differential scanning calorimetry (DSC), Fourier transform infrared (FTIR) spectroscopy, dielectric measurements, direct current magnetic susceptibility (χ_dc), and electron spin resonance (ESR). The XRD patterns revealed that the incorporation of Co particles increases the amorphization of PVAc and Co oxide formations. The DSC results suggest that the thermal properties obviously improved. Frequency and filler concentration dependence of the dielectric constant (ε′) and AC conductivity (σ_AC) were measured at room temperature in the frequency range 20 Hz to 3 MHz of pure PVAc and PVAc/Co composite films. The dielectric constant shows usual dielectric dispersion behavior. The dielectric constant and AC conductivity increased with the increase in Co content. The variation of σ_AC is attributed to hopping of polarons and bipolarons in the composites. The filling level dependence of the effective magnetic moment (μ_eff) has been evaluated. The ESR spectra exhibit a peak of an increasing depth as Co content increases. The control of thermal stability, dielectric and magnetic moment of the composites films is interesting for applications such as electric and magnetic sensors. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Preparation and characterization of biodegradable polymer blends from poly(3‐hydroxybutyrate)/poly(vinyl acetate)‐modified corn starch

Biodegradable polymer blends prepared by blending poly(3‐hydroxybutyrate) (PHB) and corn starch do not form intact films due to their incompatibility and brittle behavior. For improving their compatibility and flexibility, poly(vinyl acetate) (PVAc) was grafted from the corn starch to prepare the PVAc‐modified corn starch (CSV). The resulting CSV consisted of 47.2 wt% starch‐g‐PVAc copolymer and 52.8 wt% PVAc homopolymer and its structure was verified by FT‐IR analysis. In comparison with 35°C of the neat PVAc, the glass transition temperature (T_g) of the grafted PVAc chains on starch‐g‐PVAc was higher at 44°C because of the hindered molecular mobility imposed from starch on the grafted PVAc. After blending PHB with the CSV, structure and thermal properties of the blends were investigated. Only a single T_g was found for all the PHB/CSV blends and increased with increasing the CSV content. The T_g‐composition dependence of the PHB/CSV blends was well‐fitted with the Gordon‐Taylor equation, indicating that the CSV was compatible with the PHB. In addition, the presence of the CSV could raise the thermal stability of the PHB component. It was also found that the presence of the PHB and PVAc components would not hinder the enzymatic degradation of the corn starch by α‐amylase. POLYM. ENG. SCI., 55:1321–1329, 2015. © 2015 Society of Plastics Engineers     

The production of flexible and transparent conductive films of carbon nanotube/graphene networks coordinated by divalent metal (Cu, Ca or Mg) ions

Divalent metal ions (M²⁺, M = Cu, Ca or Mg) are used to coordinate oxidized carbon nanotubes (CNTs) and chemically modified graphene (CMG) by the oxygen-containing functional groups. Flexible and transparent conductive films of M²⁺-coordinated CNT/CMG networks are produced by spin coating. The lowest sheet resistance is 680 Ω/sq at 86% transmittance. Chemical doping with SOCl₂ further decreases the value to 370 Ω/sq with only 1% loss in transmittance. The M²⁺-coordinated CNT/CMG films can withstand 200 bending cycles without losing much in sheet resistance. This method provides a new route to transparent electrode materials with high flexibility and strength.     

Development and Characterisation of Electrically Conductive Polymeric‐Based Blends for Proton Exchange Membrane Fuel Cell Bipolar Plates

The main objective of this work was to develop films with controlled dimensions for proton exchange membrane fuel cell (PEMFC) bipolar plates (BPPs) using the twin‐screw extrusion process. These films consisted of a low‐viscosity polyethylene terephthalate (PET) in which a mixture of high specific surface area carbon black (CB) and synthetic flake graphite (GR) were dispersed. A third conductive additive, consisting of silver‐coated glass particles (SCG) or multi‐walled carbon nanotubes (MWCNT), was also added at a low concentration (5 wt.‐%) in order to study its synergistic effect on the PET‐based blend electrical conductivity. As the developed blends had to meet properties suitable for PEMFC bipolar plate applications, they were characterised for their electrical through‐plane resistivity, mechanical properties and oxygen permeability. Through‐plane electrical resistivity of about 0.3 Ω·cm and oxygen permeation rate of 3.5 × 10^–8 cc cm^–2 s^–1 were obtained for only 30 wt.‐% of a 60:40 mixture of CB/GR conductive additives. Although the substitution of 5 wt.‐% of CB/GR by the same amount of MWCNT had no significant effect on BPPs' electrical resistivity, it helped to improve their mechanical properties and especially their oxygen permeation, which was decreased from 3.5 × 10^–8 cc cm^–2 s^–1 to around 0.6 × 10^–8 cc cm^–2 s^–1.     

Silver-plated polyamide fabrics with high electromagnetic shielding effectiveness performance prepared by in situ reduction of polydopamine and chemical silvering

In this article, the silver-plated polyamide fabrics (SPPAFs) with high electroconductibility and shielding effectiveness were fabricated by using in situ reduction of polydopamine and chemical silvering. The effects of SPPAFs dopamine (C₈H₁₁O₂N) and silver nitrate (AgNO₃) concentration on surface resistivity and electromagnetic interference shielding effectiveness were studied. The results showed that the surface resistivity of SPPAFs can reach a minimum value of 0.06 ± 0.014 Ω cm⁻¹, when C₈H₁₁O₂N concentration is 4 g L⁻¹ and the AgNO₃ concentration is 120 g L⁻¹. The shielding effectiveness of SPPAFs in the wide frequency range of 10–3000 MHz increases with the increase in the concentration of AgNO₃, and increases first and stabilizes afterward with increasing C₈H₁₁O₂N concentration. When the concentration of C₈H₁₁O₂N and AgNO₃ is 3 and 120 g L⁻¹, respectively, mean shielding effectiveness values in the low-, medium-, and high-frequency bands are 71.3, 73.8, and 76.1 dB, respectively. Moreover, the mean shielding effectiveness values is 83.79 dB in the frequency range of 1.2–2.3 GHz. The dominant shielding mechanism of SPPAFs is the reflected electromagnetic waves and the absorption shielding effectiveness is less than 2 dB. The average electromagnetic shielding values of SPPAFs are above 67 dB after 16 weeks of storage, when C₈H₁₁O₂N concentration is 4 g L⁻¹ and the AgNO₃ concentration is 80 and 100 g L⁻¹. The prepared SPPAFs show promising applications in military textiles and smart wearable clothing. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 48227.     

Studies on the preparation and properties of conductive polymers. IV. Novel method to prepare metallized plastics from metal chelates of polymides–imides

A new type of polyamide–imides (PAI) was synthesized by direct polycondensation. A series of polyamide–imide metal chelate films was prepared by the transition-metal salts (AgNO₃, CuCl₂, and CoCl₂) mixed with the polyamide–imides in NMP solution. These polyamide–imide metal chelate films were reduced by various reducing agents, and the reduced films exhibited low surface resistivity around 10⁰?10¹ Ω/cm². The surfaces of these conductive films were proved to be metallized by means of X-ray analysis. The metal adhered on the film was believed to be responsible for the improvement of electrical conductivity. The effects of kinds and concentrations of metal salts, kinds and concentrations of reducing agents, and reduction time on the conductivity of metallized films were investigated. The IR spectra and SEM observations of unreduced and reduced polymer chelate films were also studied.     

Crystallization behavior and UV‐protection property of PET‐ZnO nanocomposites prepared by in situ polymerization

The aim of this study was to investigate the crystallization behavior and UV‐protection property of polyethylene terephthalate (PET)‐ZnO nanocomposits. PET‐ZnO nanocomposites containing 0.5–3.0 wt % of ZnO were successfully synthesized by in situ polymerization. The Fourier transformed infrared (FTIR) spectroscopy indicated the silane coupling agent was anchored onto the surface of ZnO. Scanning electron microscope (SEM) images showed ZnO particles were dispersed homogeneously in PET matrix with amount of 0.5–1.0 wt %. Differential scanning calorimetry (DSC) results exhibited that the incorporation of ZnO into PET resulted in increase of the melting transition temperature (T_m) and crystallization temperature (T_c) of PET‐ZnO nanocomposites. The crystallization behavior of PET and PET‐ZnO nanocomposites was strongly affected by cooling rate. ZnO nanoparticles can act as an efficient nucleating agent to facilitate PET crystallization. UV–vis spectrophotometry showed that UV‐ray transmittance of PET‐ZnO nanocomposites decreased remarkably and reached the minimum value of 14.3% with 1.5 wt % of ZnO, compared with pure PET whose UV‐ray transmittance was 84.5%. PET‐ZnO nanocomposites exhibited better UV‐protection property than pure PET, especially in the range of UVA. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Preparation and barrier property of poly(ethylene terephthalate)/clay nanocomposite using clay‐supported catalyst

Poly(ethylene terephthalate) (PET)/clay nanocomposite was prepared by the direct polymerization with clay‐supported catalyst. The reaction degree of catalyst against the cation exchange capacity of clay was 8 wt %. The intercalation of PET chains into the silicate layers was revealed by X‐ray diffraction studies. SEM morphology of the nanocomposite showed a good dispersion of clay‐supported catalyst, ranging from 30 to 100 nm. The intercalated and exfoliated clay‐supported catalyst in PET matrix was also observed by TEM. The improvement of O₂ permeability for PET/clay‐supported catalyst composite films over the pure PET is approximately factors of 11.3–15.6. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 4875–4879, 2006     

Shielding effectiveness of carbon‐filled polycarbonate composites

In this project, varying amounts of three different carbons [carbon black (CB), carbon nanotubes (CNT), and graphene nanoplatelets (GNP)] were added to polycarbonate (PC). The resulting single filler composites were tested for shielding effectiveness (SE). The effects of single fillers and combinations of two different carbon fillers were studied via a factorial design. At the highest single filler loadings, the following SE results were obtained at 800 MHz: 18.9 dB for 10 wt % CB/PC, 18.4 dB for 8 wt % CNT/PC, and 6.3 dB for 15 wt % GNP/PC. The highest SE value of 21.4 dB was measured for the 5 wt % CB/5 wt % CNT/PC composite and could be used in SE applications (typically > 20 dB is needed). Statistically significant equations were developed that could be used to predict the SE of composites containing these fillers. In addition, it was determined that the composite SE is higher than what would be expected from the additive effect of each single filler for the CB/GNP/PC composites. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42719.     

Transparent conductive film based on carbon nanotubes and PEDOT composites

Single-walled nanotubes (SWNTs), thin multiwalled carbon nanotubes (t-MWNTs) and multiwalled carbon nanotubes (MWNTs) were treated with H₂SO₄–HNO₃ acid solution, under different chemical conditions. The acid-treated CNTs were dispersed in DI water and in poly (3,4-ethylenedioxythiophene) (PEDOT) solution. Furthermore, the finely dispersed CNTs/PEDOT solutions were employed to a simple method of bar coating to obtain the transparent conductive films on the glass and polyethylene terephthalate (PET) film. A sheet resistance of 247 Ω/sq and a transmission of 84.7% were obtained at a concentration of the acid-treated CNTs of 0.01 wt.%.     

Electroless silver plating on the PET fabrics modified with 3‐mercaptopropyltriethoxysilane

The feasibility of adherent silver layers onto PET fabrics by electroless plating was explored and its optimal technology for modification and electroless plating was investigated. Morphology, structure, and thermal stability of silver plating PET fabrics were characterized by scanning electric microscope (SEM), X‐ray diffraction (XRD) and thermogravitric (TG) analysis. As the silver weight on the modified fabric is 25 g/m², the electromagnetic shielding effectiveness (SE) of silver plating PET fabric is more than 30dB at the frequency ranging from 1MHz to 5000 MHz. The results show that the silver plating PET fabric has good electrical conductivity and electromagnetic shielding property. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012