Preparation and characterizations of polypyrrole on liquid ammonia pre-treated wool fabric

Wool fabric was treated with liquid ammonia at -40 °C for 30 and 60 s prior to the application of polypyrrole (PPy). The polymer was deposited on wool fiber using the chemical oxidation method with 0.02 and 0.05 mol/l (Py) monomer concentration and FeCl₃ as a catalyst. Functional groups of wool samples were analyzed using FT-IR, and surface morphology was investigated using SEM micrographs. Properties such as water absorbency, surface resistivity, abrasion resistance, weight add-on, and air permeability of coated specimens were explored. The FT-IR outcomes revealed the liquid ammonia pre-treatment changed the amount of amide I (NH), cystic acid, cystic monoxide, and dioxide content of the fiber. SEM micrographs revealed the descaling of wool surface after pre-treatment and smooth coating of polymer. Pre-treatment of wool in liquid ammonia improved absorbency of wool fabric with respect to the treatment duration. The surface resistivity of wool fabric decreased with the increase of monomer concentration and pre-treatment duration. The results of abrasion resistance confirmed that the pre-treated fabric exhibited lower loss of polymer after 200 cycles of abrasion. The weight of the fabric was increased and air permeability decreased when the monomer concentration and liquid ammonia pre-treatment duration was increased.     

Decay of electrical conductivity in p-toluene sulfonate doped polypyrrole films

Long term performance of conductivity of p-toluene sulfonic acid (pTSA) doped electrochemically synthesized polypyrrole (PPy) films was estimated from accelerated aging studies between 80 °C and 120 °C. Conductivity decay experiments indicated that overall aging behavior of PPy films deviated from first order kinetics at prolonged aging times at elevated temperatures. However, an approximate value for the activation energy of the conductivity decay of PPy was calculated as E=47.4 kJ/mol, enabling an estimate of a rate constant of k=8.35×10⁻⁶/min at 20 °C. The rate of decrease of conductivity was not only temperature dependent but also influenced by the dopant concentration. A concentration of 0.005 M pTSA in the electrolyte resulted in a conductive film and when this film was exposed to 120 °C for a period of 40 h, the conductivity decayed to about 1/20 of its original value. The concentration of pTSA was increased to 0.05 mol/l and when the resulting film was aged in the same way, it showed a decrease in the conductivity to about 1/3 of its original value. Both microwave transmission and dc conductivity data revealed that highly doped films were considerably more electrically stable than lightly doped films. The dopant had a preserving effect on the electrical properties of PPy.     

Properties and performance of polypyrrole (PPy)-coated silk fibers

Different silk substrates in form of spun silk tops, nonwoven web, yarn, and fabric were coated with electrically conducting doped polypyrrole (PPy) by in situ oxidative polymerization from an aqueous solution of pyrrole (Py) at room temperature using FeCl₃ as catalyst. PPy-coated silk materials were characterized by optical (OM) and scanning electron (SEM) microscopy, FT-IR spectroscopy, and thermal analysis (DSC, TG). OM and SEM showed that PPy completely coated the surface of individual silk fibers and that the polymerization process occurred only at the fiber surface and not in the bulk. Dendrite-like aggregates of PPy adhered to the fiber surface, with the exception of the sample first polymerized in the form of tops and then spun into yarn using conventional industrial machines. FT-IR (ATR mode) showed a mixed spectral pattern with bands typical of silk and PPy overlapping over the entire wavenumbers range. DSC and TG showed that PPy-coated silk fibers attained a significantly higher thermal stability owing to the protective effect of the PPy layer against thermal degradation. The mechanical properties of silk fibers remained unchanged upon polymerization of Py. The different PPy-coated silk materials displayed excellent electrical properties. After exposition to atmospheric oxygen for two years a residual conductivity of 10–20 % was recorded. The conductivity decreased sharply under the conditions of domestic washing with water, while it remained essentially unchanged upon dry cleaning. Abrasion tests caused a limited increase of resistance. PPy-coated silk tops were successfully spun into yarn either pure or in blend with untreated silk fibers. The resulting yarns maintained good electrical properties.     

Conductive cotton fabrics for heat generation prepared by mist polymerization

Cotton fabrics were coated with conducting polypyrrole (PPy) by mist polymerization derived from aqueous solution of pyrrole (Py) with ferric chloride (FeCl₃) as oxidant. The polymerization conditions, such as the reaction time and the concentrations of monomer and oxidant, were systematically investigated. The prepared PPy-coated fabrics could keep their temperature at about 24–44 °C when charged by a fixed DC voltage of 1–3 V. The results indicate that these PPy-coated fabrics can be used potentially as heating pads and integrated into the apparel to make the wearer warm enough using a portable battery. Furthermore, such fabrics are more comfortable than the conventional heating pads due to their flexibility and breathability.     

Synthesis and characterization of electrically conductive composite films of polypyrrole/poly(acrylonitrile-co-styrene)

Homogeneus Polypyrrole (PPy)/poly(acrylonitrile-co-styrene) (SAN) composite thin films were prepared by chemical polymerization of pyrrole on poly(acrylonitrile-co-styrene) matrix. Ce (IV) is used as an oxidant for in-situ polymerizion of pyrrole on SAN matrix, having an advantageous over the impregnation method. The formation and incorporation of PPy in the copolymer matrix were confirmed by FTIR-ATR and UV-Visible spectrophotometric measurements. Thermal analyses showed that after polymerization of Py in copolymer matrix, thermal behavior of SAN was changed and derivative of weight loss at this temperature was increased by increasing of PPy content. XPS and FTIR-ATR analysis of composite films indicated cerium salt with nitrate ion acted as a dopant. The increase in the AC electrical conductivity of the PPy/SAN composites over pure SAN was observed. At lower frequency up to 10⁵ Hz, conductivity was shown an independent behavior from frequency; but at high frequencies (10⁵–10⁷ Hz), dependence on frequency was explained by polaron and bipolaron formations of PPy. The dispersion of PPy particles in copolymer matrix was proven by SEM, AFM and digital camera. By the increase of PPy content in the composite films, increase in AC conductivities, and decrease in dielectric constants and loss were observed.     

Gold recovery using inherently conducting polymer coated textiles

The ability of inherently conducting polymer (ICP) coated textiles to recover gold metal from aqueous solutions containing [AuCl₄]⁻ was investigated. Nylon-lycra, nylon, acrylic, polyester and cotton were coated with a layer of polypyrrole (PPy) doped with 1,5-naphthalenedisulfonic acid (NDSA), 2-anthraquinonesulfonic acid (AQSA) orp-toluenesulfonic acid (pTS). Textiles coated with polyaniline (PAn) doped with chloride were also used. The highest gold capacity was displayed by PPy/NDSA/nylon-lycra, which exhibited a capacity of 115 mg Au/g coated textile, or 9700 mg Au/g polymer. Varying the underlying textile substrate or the ICP coating had a major effect on the gold capacity of the composites. Several ICP coated textiles recovered more than 90% of the gold initially present in solutions containing 10 ppm [AuCl₄]⁻ and 0.1 M HCl in less than 1 min. Both PPy/NDSA/nylon-lycra and PAn/Cl/nylon-lycra recovered approximately 60% of the gold and none of the iron present in a solution containing 1 ppm [AuCl₄]⁻, 1000 ppm Fe³⁺ and 0.1 M HCl. The spontaneous and sustained recovery of gold metal from aqueous solutions containing [AuCl₄]⁻ using ICP coated textiles has good prospects as a potential future technology.     

Microstructure and properties of Ni-Fe3O4 composite plated polyester fabric

In this study, electroless Ni-Fe₃O₄ composite plating on polyester fabric modified with 3-aminopropyltrimethoxysilane (APTMS) was investigated under ultrasonic irradiation. Effects of deposit weight on microstructure and properties of Ni-Fe₃O₄ composite coating were studied. Surface morphology, chemical composition and state, crystal structure of the electroless Ni-Fe₃O₄ composite plated polyester fabric were characterized by SEM, EDX, XPS and XRD. Magnetic properties, electrical resistivity and electromagnetic interference (EMI) shielding effectiveness (SE) of Ni-Fe₃O₄ plated polyester fabric were also evaluated. The presence of co-deposition of Fe₃O₄ in Ni coating on the polyester fabric is demonstrated by an XPS analysis. At a higher deposit weight, there is an increase in particle size and saturation magnetization, and a decrease in electrical resistivity with respect to the rise of deposit weight, respectively. As the Ni-Fe₃O₄ weight on the treated fabric is 32.90 g/m², the EMI SE of the Ni-Fe₃O₄ plated polyester fabric arrives 15–20 dB at frequencies that range from 8 to 18 GHz. The results indicate the Ni-Fe₃O₄ plated polyester fabrics are used as super-paramagnetic, conductive and EMI shielding materials.     

An extensive look into the effect of mercerization treatment on dimensional properties of cotton plain knitted fabric

Following our previous research [1], an extensive investigation on the effects of four mercerization treatment parameters namely, alkali concentration, time of treatment, bath temperature, and mercerization tension on dimensional properties of plain knitted fabric produced from cotton yarn is presented in this paper. Numerical values of constant geometry of the dry relaxed, wet relaxed, and mercerized samples were calculated according to Munden’s equations. Study shows that the area geometry constant values (K _s ) achieved after mercerization treatment was higher than values obtained for the samples subjected to dry and wet relaxations. Also, ANOVA test confirmed significant effects of each parameter itself and their interactions on dimensional properties of the fabric samples. Based on the results, applying less value of tension improves dimensional stability of the fabric but not for the samples mercerized in higher values of three other parameters. The alkali concentration had an optimum value in mercerization treatment. In mercerizing conditions carried out in high temperature and long time, lower alkali concentration is more efficient. Increasing time of treatment leads to achieve higher K _s value when lower value of alkali concentration is used. Most of the samples mercerized in bath temperature of 40 °C had the highest K _s . At the end of the research a statistical model was derived to predict the area geometry constant of the fabric.     

Evaluation of bamboo charcoal/stainless steel/TPU composite woven fabrics

Composite woven fabric satisfies what people require. Bamboo charcoal (BC) has been identified as a multifunctional material that has far-infrared ray, anions, deodorization and etc. BC fibers and yarns were made of bamboo charcoal powders and have further become a pervasive materials used in textile industry. In this study, cotton yarns, stainless steel/cotton (SS/C) complex yarn, bamboo charcoal/cotton (BC/C) complex yarns were woven into the plain, twill and Dobby composite woven fabrics. The warp yarn was composed of cotton yarns, and the weft yarn was made up of BC/C and SS/C complex yarns with a picking ratio of 1:1 and 3:1. Thermoplastic polyurethanes (TPU) film was then attached to the composite woven fabrics, forming the BC/SS/TPU composite woven fabrics. Tests of electromagnetic shielding effectiveness (EMSE), far-infrared emissivity, anions, water resistance, and water vapor permeability measured the single-layer, two-layer and four-layer composite woven fabrics, obtaining a far-infrared emissivity of 0.95 by 39.8 counts per minute, an anion count of 149 amount/cc, an EMSE of −11.87 dB under frequency of 900 MHz, a surface resistivity of 8×10⁻⁶ Ω/square, a water resistance of −8219 mmH₂O, and water vapor permeability of 989 g/m²·h and 319 g/m²·24 h in accordance with JIS L 1099 A1 and ASTM E96 BW.     

Preparation of electroconductive,magnetic, antibacterial,and ultraviolet-blocking cotton fabric using reduced graphene oxide nanosheets and magnetite nanoparticles

The main goal of present study was the fabrication of cotton fabric with special functions, including electrical conductivity, magnetic, antibacterial, and ultraviolet (UV) blocking. In this regard, the cotton fabric was primarily coated with graphene oxide and then reduction of graphene oxide and synthesis of magnetite nanoparticles accomplished in one step. The alkaline hydrolysis of magnetite precursors and reduction of graphene oxide was simultaneously performed using sodium hydroxide to produce reduced graphene oxide/Fe₃O₄ nanocomposite on the fabric surface. The prepared cotton fabrics were characterized with field emission scanning electron microscope (FE-SEM), X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDS), and X-ray photoelectron spectroscopy (XPS). The treated fabrics with reduced graphene oxide/Fe₃O₄ nanocomposite displayed a low electrical resistivity i.e. 80 kΩ/sq. Furthermore, the coated fabrics showed reasonable magnetic properties due to the presence of magnetite nanoparticles on the surface of cotton fabrics. Moreover, this process imparted proper antibacterial properties and UV blocking activity to cotton samples.     

Dimensional stabilization of cotton plain weft knitted fabric using mercerization treatment

Investigation on dimensional stability of cotton plain weft knitted fabric manufactured from rotor spun yarn, subjected to mercerization treatment has been represented. Several fabric samples were mercerized considering variation in time of treatment, bath temperature, concentration of alkali solution and also mercerizing tension. Values of constant of course (K _c ), constant of wale (K _w ), the area geometry constant (K _s ) which are indicative of fabric dimensional stability were calculated after treatment for mercerized samples. Then, these values were compared with those of un-treated samples subjected to dry and wet relaxation and also were compared with each other. Based on the effect of each variable itself and their simultaneous effect, it was concluded that, mercerization treatment and considered parameters had a distinctive influence on dimensional stability of the fabric. Mercerized samples had better dimensional stability in comparison with un-treated ones. A comprehensive experimental analysis showed that, there is meaningful difference between K _s values of the samples mercerized at various conditions. Also, the area geometry constant (K _s ) achieved after treatment was higher than that of other relaxation methods.     

Inhibition of Iron Induced Lipid Peroxidation and Antioxidant Activity of Indian Spices and Acacia In Vitro

The spices used in the Indian foods such as Star anise (Illicium verum), Bay leaves (Cinnamomum zeylanicum) and Cobra’s saffron (Mesua ferrea), and Acacia (Acacia catechu), which have medicinal value, were used as test samples, to find their effect on in vitro lipid peroxidation (LPO). Rat liver post mitochondrial supernatant (PMS) in Tris HCl buffer, pH 7.4 was incubated for 0 and 1 h, with various test extracts in three different oxidant systems. The results show that addition of test samples to FeCl₃ medium at 0 h significantly stop the initiation of the LPO. However, the propagation phase of LPO was inhibited by Cobra’s saffron and Acacia and not by Star anise and Bay leaves. The test samples also showed strong reducing power and superoxide radical scavenging activity. Cobra’s saffron and Acacia showed the highest antioxidant activity, probably due to the higher polyphenol content as compared to other test samples.     

Preparation and property of TiO2/SiO2 multilayer film on the fabric by sol-gel process

The high light reflection of multilayer TiO₂/SiO₂ film was prepared on the fabric by the sol-gel process. The size of titania and silica particles in hydrosol was analyzed by Nanosizer, and the morphology of TiO₂/SiO₂ multilayer film on the fabric was characterized by SEM. The reflection spectra of the samples were tested accordingly, and it showed that the reflection of the fabric coated by multilayer film was higher than that of the monolayer film. Moreover, the reflection increased with the increase of layer number. For sunlight fastness testing, the fabric color changed less with the increase of layer number, which showed the multilayer film on the fabric can improve the light resistance of the fabric. The mechanical property, the bending property and air permeability testing results showed that there was little change for the coated fabric compared with the original fabric.     

Platinum recovery using inherently conducting polymers and common fabrics

The recovery of platinum from solutions containing [PtCl₆]²⁻ using inherently conducting polymer (ICP) powders, membranes and coated fabrics has been investigated. Polyaniline (PAn) powders were able to recover platinum from solution, whereas polypyrrole (PPy) powders and membranes displayed almost no ability to perform this task. Uncoated pieces of nylon and nylon-lycra showed a significant capacity to recover platinum metal, unlike each of the other common fabrics investigated. Surprisingly the amount of platinum recovered by nylon-lycra was not improved by coating the fabric with a layer of ICP. Pieces of nylon-lycra that had previously been soaked in solutions containing [PtCl₆]²⁻ released only a small percentage of the bound metal when treated with 5 % HCl. However, subsequent treatment with aqua regia released all of the remaining platinum. A mechanism of platinum recovery by nylon and nylon-lycra involving coordination to functional groups present in their polymeric structures is proposed.     

Preparation and properties of polypropylene nanocomposites reinforced with exfoliated graphene

We have prepared a series of polypropylene/exfoliated graphene (PP/EG) nanocomposite films via efficient meltcompounding and compression, and investigated their morphology, structures, thermal transition behavior, thermal stability, electrical and mechanical properties as a function of EG content. For the purpose, EG, which is composed of disordered graphene platelets as reinforcing nanoscale fillers, is prepared by the oxidation/exfoliation process of natural graphite flakes. SEM images and X-ray diffraction data confirm that the graphene platelets of EG are well dispersed in PP matrix for the nanocomposites with EG contents less than 1.0 wt%. It is found that thermo-oxidative degradation of PP/EG nanocomposites is noticeably retarded with the increasing of EG content. Electrical resistivity of the nanocomposite films was dramatically changed from ∼10¹⁶ to ∼10⁶ Ω·cm by forming electrical percolation threshold at an certain EG content between 1 and 3 wt%. Tensile drawing experiments demonstrate that yielding strength and initial modulus of PP/EG nanocomposite films are highly improved with the increment of EG content.     

Structural investigation of anionic functional poly(vinyl alcohol) doped polypyrrole nanospheres

This article reports on a facile route for the preparation of polypyrrole nanospheres with improved water solubility, ordering and conductivity in the presence of a polyelectrolyte, such as phosphorylated polyvinyl alcohol. The phosphorylated polyvinyl alcohol (PPVA) was used as both the stabilizer and the dopant in the chemical oxidative polymerization of pyrrole. The resulting PPVA doped polypyrrole (PPy) nanocomposites (PPy-PPVA) were characterized with FTIR, TGA, SEM and AFM techniques. The electrical conductivity of polymer was measured by four-point probe method. Our observation and results suggest a plausible formation mechanism of PPy nanospheres, PPVA micelle might have functioned as ‘template’ during the polymerization of pyrrole monomers, meanwhile, the PPy chains doped with phosphate group. It was found that the size decreased and their dispersion stability in water increased with the increasing feeding ratio of PPVA. The conductivity of PPy with different morphologies was also measured and compared. When the PPVA: pyrrole feeding ratio ranged from 20 to 50 wt%, the PPy-PPVA nanoparticles showed spherical shape with excellent uniformity, good electrical conductivity (up to 33.1 S·cm^?1), and weakly temperature dependent conductivity. It’s worth mentioning that the PPy-PPVA nanocomposite prepared in high PPVA feeding ratio has been well-dispersed for more than 24 months, which indicates its significant dispersion stability.     

Effects of ferric chloride on structure, surface morphology and combustion property of electrospun polyacrylonitrile composite nanofibers

In this work, the pure polyacrylonitrile (PAN) nanofibers and PAN/FeCl₃ composite nanofibers were prepared by an electrospinning process. Electrospinning solution properties including viscosity, surface tension and conductivity, had been measured and combined with the results of Scanning electron microscopy (SEM), Atomic force microscope (AFM) and Micro Combustion Calorimeter (MCC) to investigate the effects of FeCl₃ on the structure, surface morphology and combustion property of electrospun PAN nanofibers, respectively. It was found from SEM images that the diameters of composite nanofibers were decreased with the addition of FeCl₃, which was attributed predominantly to the increased conductivity of the polymer solutions compared to viscosity and surface tension. The AFM analyses revealed that the surface morphology of electrospun nanofibers changed from smooth and wrinkle-like structure (without FeCl₃) to rough and ridge-like structure (with FeCl₃). The results characterized by MCC showed that the loading of FeCl₃ decreased the heat release rate (HRR) and improved the combustion property of composite nanofibers.     

Multifunctional modification of wool fabric using graphene/TiO<Subscript>2</Subscript> nanocomposite

In this study, a new finishing technique is introduced through treatment of wool fabric with graphene/TiO₂ nanocomposite. Graphene oxide/titanium dioxide nanocomposite first applied on the wool fabric by hydrolysis of titanium isopropoxide in graphene oxide suspension and then this coating chemically converted by sodium hydrosulfite to graphene/TiO₂ nanocomposite. The homogenous distribution of the graphene/TiO₂ nanocomposite on the fiber surface was confirmed by field emission scanning electron microscopy (FE-SEM), Energy-dispersive X-ray spectroscopy (EDS) and X-ray mapping. X-ray diffraction patterns proved the presence of titanium dioxide nanoparticles with a crystal size of 127 Å on the treated wool fabric. Also, the defect analysis based on X-ray photoelectron spectroscopy (XPS) established the composition of the nanocomposite. Other characteristics of treated fabrics such as antibacterial activity, photo-catalytic self-cleaning, electrical resistivity, ultraviolet (UV) blocking activity and cytotoxicity were also assessed. The treated wool fabrics possess significant antibacterial activity and photo-catalytic self-cleaning property by degradation of methylene blue under sunlight irradiation. Moreover, this process has no negative effect on cytotoxicity of the treated fabric even reduces electrical resistivity and improves UV blocking activity.     

Performance of cotton fabric treated with an amino-terminated hyperbranched polymer

An amino-terminated hyperbranched polymer (HBP-NH₂), synthesized from methyl acrylate and diethylene tri-amine by polycondensation, was applied to treat cotton samples by a pad-dry-cure method. Physical properties, salt-free dye-ability, antimicrobial activity, and antiultraviolet property of the treated cotton samples were tested. The crystallinity and mechanical properties, including breaking strength, breaking elongation, and Young’s modulus of the treated cotton fibers, increased slightly in comparison with those of the untreated cotton fibers. The thermal stability and the moisture regain were also improved slightly. Dyed with direct dyes and reactive dyes in the absence of the electrolytes, the treated cotton fabric showed similar or higher color strength compared with the untreated cotton fabric in conventional dyeing. The treated cotton fabric can also be dyed with acid dyes effectively. In addition, the treated cotton fabric showed good antimicrobial activities against Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli). The study of the antiultraviolet properties of the treated cotton fabric indicated that the HBP-NH₂ contributed to the reduction of UV transmission and the increase of UPF.     

Surface characterization of aromatic thermotropic liquid crystalline fiber deposited by nanostructured silver

Nanostructured silver thin films were sputtered onto the aromatic thermotropic liquid crystalline fibers of Vectran by magnetron sputtering technology. Plasma treatment was used as pre-treatment in order to improve the deposition of the coating layer. Surface morphology of the coated fibers was examined by scanning electron microscopy (SEM) and atomic force microscopy (AFM). A full energy dispersive X-ray analysis (EDX) was used to detect the elemental composition of the material. Its conductivity and mechanical properties were measured and analyzed as well. The study revealed that a very thin conductive silver deposition exhibited high electrical conductivity as well as less influence on the mechanical properties of the pre-treated Vectran fiber. The plasma treatment could improved the deposition of the coating layer, but the surface roughness caused by plasma treatment also affected the surface conductivity. It was found that the surface resistivity could reach very low value of 1.66×10⁻³ Ω·cm after sputtering deposition for 30 min.