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.     

Functional Antibacterial Finishing of Woolen Fabrics Using Ultrasound Technology

The growing concern for the personal health and hygiene has created the necessity of acquiring wool fabric antibacterial activity. Silicon dioxide nanoparticles (SiO₂ NPs) have appropriate features to enhance the functional properties of wool fabrics, especially with polymer application. In this study efficient coating using polyethylene glycol (PEG₂₀₀₀) and SiO₂ NPs were used for imparting antibacterial properties to treated fabrics. All the treatments were carried out using both conventional and ultrasound techniques. The physical and chemical properties were evaluated using FTIR, XRD, and SEM. The result indicated that treated wool fabrics by PEG/SiO₂ NPs improved the dyeability and antibacterial of the fabrics and also enhanced its mechanical properties. Furthermore, it is believed that the ultrasound radiation causes homogeneous distribution of cross-links and polymerization throughout the wool surface. This offers considerable advantages compared to conventional treatment.     

Functional modification of wool fabric by thiol-epoxy click chemistry

The paper reports modification and characterization of wool fabrics achieved through thiol-epoxy click chemistry. A pretreatment with tris (2-carboxyethyl) phosphine (TCEP) as an effective reducing agent was carried out to produce thiol groups on wool surface. Glycidyl trimethyl ammonium chloride (GTAC) was later covalently bonded with wool fibers via thiol-epoxy reaction. The reaction was confirmed by SEM, FTIR, Raman and TG analysis. Antibacterial activity, antistatic property, hydrophilicity and dyeability of treated wool fabric were assessed. The results demonstrated that TCEP-GTAC treatment can endow wool fabric good antibacterial and antistatic properties as well as improved hydrophilicity. Tensile strength studies indicated fiber strength loss of ~12 % on modification.     

Application of silver nanoparticles as an antibacterial mordant in wool natural dyeing: Synthesis,antibacterial activity,and color characteristics

Madder is a natural colorant which is commonly applied with metal salts as a mordant to improve its affinity to fibers and color fastness. Madder produces an insoluble complex or lake in the presence of metal ions on mordanted fabric. In this study, wool fabric was pretreated with AgNPs (silver nanoparticles) as a mordant, then dyed with madder. The wool fabric samples were examined by scanning electron microscopy (SEM) and their colorimetric characteristics were evaluated. The formation of spherical silver nanoparticle was confirmed using UV-Visible spectroscopy, SEM images, and elemental analysis. The average size of synthesized silver nanoparticles on the surface of wool fibers is around 73 nm. The dyed wool samples were pretreated with different concentration of Ag⁺ ions or AgNPs, which showed higher color strength value compared to untreated dyed wool fabric. This pretreatment also presented good antibacterial activity.     

Antibacterial Coating of Glass Fiber Filters with Silver Nanoparticles (AgNPs) and Glycidyltrimethylammonium Chloride (GTAC)

Silver nanoparticles (AgNPs) were attached to glass fiber filters to improve their antibacterial properties using glycidyltrimethylammonium chloride (GTAC), a type of quaternary ammonium salt. The glass fiber filters treated with GTAC were placed into the Ag colloid and heat-treated at 43 °C for 90 min to attach AgNPs to the glass fiber filters. The glass fiber filters with the attached AgNPs were then analyzed by scanning electron microscopy and atomic force microscopy (AFM). The surface morphology of the glass fiber filters treated with GTAC and AgNPs was observed. The Ag atomic % of the glass fiber filters was analyzed according to the GTAC concentration, Ag colloid concentration, and AgNPs treatment temperature. The surface roughness of the glass fiber filters with the attached AgNPs was measured by AFM. The antibacterial tests of the GTAC and AgNP-treated glass fiber filters highlighted the sufficient antibacterial effects against E. coli, S. aureus, and P. aeruginosa. In particular, the antibacterial properties of glass fiber filters against S. aureus and P. aeruginosa were improved when the glass fiber filters were treated with both GTAC and AgNPs.     

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.     

Synthesis and characterization of nanocrystalline CoWO4@silk fibers with antibacterial activity under ultrasound irradiation

The present investigation reports the novel synthesis of CoWO₄ nanoparticles@silk fiber under ultrasound irradiation. The effect of temperature, power of ultrasound irradiation and sequential dipping steps in growth of the CoWO₄ particles were studied. Results show a decrease in the particles size as the temperature and power of irradiation decreased. The fibers containing CoWO₄ nanoparticles were tested for their antibacterial efficacy against E. coli and S. aureus and were found to possess significant antibacterial activity. The results show the CoWO₄ nanoparticles@silk with strongest fluorescence characteristics can be obtained in this method. The physicochemical properties of the nanoparticles were determined by X-ray diffraction (XRD), scanning electron microscopy (SEM) and fluorescence spectroscopy.     

The effects of wool surface characteristic on fuzzing and pilling of knitted fabrics

The fuzzing and pilling of untreated, chlorinated and oxidized wool knitted fabrics were compared with frictional coefficients measured by capstan method, surface modification observed by scanning electron microscopy (SEM), the surface roughness and the scale height assessed by atomic force microscopy (AFM), and hairiness imaged on the three-dimensional rotational microscopy. The pilling comparative experiments of the corresponding knitted fabrics were conducted by means of Pillbox method. Experimental results showed that some scales on the oxidized fiber surface were partially cleaved and some grooves generated. With oxidization treatment, the anti- and with-scale of friction coefficient increase with decreasing the thickness of scales and the yarn hairiness. There is good correlation between the result of AFM and the change in frictional coefficients. The pilling grade of knitted fabric comprised of oxidization wool is 2.5, and the average numbers of pills per 25 cm² is 25. It is postulated that the surface topography, the frictional properties of oxidized wool fibers and surface hairs of corresponding yarns may limit the ability of those surface fibers to form fuzz and of those fuzz for pill formation.     

Thin film deposition by PECVD using HMDSO-O<Subscript>2</Subscript>-Ar gas mixture on knitted wool fabrics in order to improve pilling resistance

In this work knitted wool fabrics were coated by a Si:O_x:C_y:H_z thin film with the aim to promote pilling resistance. The wool samples were plasma coated in a radio frequency (RF) glow discharge using hexamethyldisiloxane (HMDSO) as the precursor, in mixture with argon and oxygen gases, for different deposition times and reaction pressures, at constant discharge power. Deposited films were characterized by means of Fourier transform infrared (FTIR) spectroscopy and surface morphology by means of scanning electron microscopy; moreover, propensity to pilling of treated samples was investigated, showing that treated fabrics had a better pilling performance respect to untreated ones.     

Surface modification of cellulose fibers by layer-by-layer self-assembly of lignosulfonates and TiO2 nanoparticles: Effect on photocatalytic abilities and paper properties

Depositing of TiO₂ nanoparticles on cellulose fiber surface has potential technological applications in the field of photocatalysis. With this motivation, multilayers composed of lignosulfonates (LS) and TiO₂ nanoparticles were constructed on cellulose fiber surface via layer-by-layer (LBL) self-assembly technique. X-ray photoelectron spectroscopy (XPS), zeta potential measurement and atomic force microscopy (AFM) were used to characterize the LS/TiO₂ multilayers on cellulose fiber surface. Moreover, the photocatalytic activities of modified cellulose fibers (decomposition of methyl orange and antibacterial test) were investigated. The decomposition efficiency of methyl orange for a (LS/TiO₂)₅ multilayer modified cellulose fibers was 74.7 % under 5 h UV irradiation. Photocatalytic decomposition efficiency of methyl orange by LS/TiO₂ multilayer modified cellulose fibers under the same UV irradiation time increased linearly with the number of bilayers. Antibacterial tests results revealed that the cellulose fibers modified with LS/TiO₂ multilayers exhibited excellent antibacterial activity against E.coil. The degree of E.coil growth inhibition for a (LS/TiO₂)₅ multilayer modified cellulose fiber reached as high as 93 %. In addition, the effect of LS/TiO₂ multilayers on properties of handsheets made from modified cellulose fibers was also considered. The air permeability of the handsheet prepared from fibers modified with TiO₂/LS multilayers had 6.1–24.3 % higher compared with that of handsheet prepared from original fibers. The wetting properties measurement results demonstrated that the water contact angle of handsheet oscillated with the increasing number of layers depended on building block which was in the outermost layer.     

The effect of ultrasonication on the micro-splitting of wool fiber

In this study, normal and dichlorodicyanuric acid (DCCA)-treated wool slivers were ultrasonicated in formic acid aqueous solutions. The effect of the ultrasonication condition on the wool fiber splitting was examined and the mechanism of the splitting by ultrasonication in formic acid was elucidated. No wool fiber splitting occurred at formic acid content up to 70 %, but the fiber splitting accelerated as the formic acid content increased from 75 %. Although no fiber splitting occurred up to 450W ultrasonic power, the degree of splitting increased significantly with increasing ultrasonic power above 450W. The wool fiber splitting by ultrasonication was heterogeneous and FE-SEM observations revealed a three-step splitting process: 1) full removal of scale, 2) removal of cell membrane complex (CMC), and 3) fiber splitting. A comparison of the fiber splitting of normal and DCCA-treated wool revealed that the scale of the ultrasonication-treated wool was removed by peeling off rather than by dissolution.     

High yield preparation of keratin powder from wool fiber

A descaling and oxidation pretreatment was employed to maximize the yield of cortical cells in the disintegration process of wool fiber. The results indicated that the productivity of intact cortical cells was greatly increased by moderate oxidation pretreatment in 1.6 % per-acetic acid within 2 h, but the yield would be decreased by further oxidation pretreatment. In order to give a reasonable explanation for this fact, the effect of the increasing time of oxidation pretreatment on the yield of intact cortical cells was investigated by means of spectral analysis using FT-IR and XRD. The intensity of the peak at 1040 and 1173 cm^?1 in FT-Infrared spectrum gradually increased with increasing oxidation pretreatment time, suggesting that more and more SS bonds were cleaved to form cysteic acid. X-ray Diffraction investigation showed that the crystallinity of wool fiber obviously decreased when the time of oxidation pretreatment exceeded 2 h. The combined results of FT-IR and XRD revealed that SS bonds in the amorphous region of wool fiber were first cleaved in the fiber components. The selective cleavage of SS bonds in the amorphous region by the appropriate oxidation pretreatment can effectively decrease the bonding force between the components of wool fiber and enhance the yield of intact cortical cells.     

Dyeing behavior of low temperature plasma treated wool

In this paper, the effects of low temperature plasma (LTP) treatment on the dyeing properties of the wool fiber were studied. The wool fibers were treated with oxygen plasma and three types of dye that commonly used for wool dyeing, namely: (i) acid dye, (ii) chrome dye and (iii) reactive dye, were used in the dyeing process. For acid dyeing, the dyeing rate of the LTP-treated wool fiber was greatly increased but the final dyeing exhaustion equilibrium did not show any significant change. For chrome dyeing, the dyeing rate of the LTP-treated wool fiber was also increased but the final dyeing exhaustion equilibrium was only increased to a small extent. In addition, the rate of afterchroming process was similar to the chrome dyeing process. For the reactive dyeing, the dyeing rate of the LTP-treated wool fiber was greatly increased and also the final dyeing exhaustion equilibrium was increased significantly. As a result, it could conclude that the LTP treatment could improve the dyeing behavior of wool fiber in different dyeing systems.     

Electrospun grape seed polyphenols/gelatin composite fibers contained silver nanoparticles as biomaterials

GSP/gelatin composite nanofiber membranes containing silver nanoparticles were successfully fabricated as a novel biomaterial by electrospinning. The silver nanoparticles (AgNPs) were synthesized with the grape seed polyphenols (GSP) as reducing agent in aqueous solution of gelatin, and then the GSP/gelatin/AgNPs mixed solution was electrospun into nanofibers at 55 °C. The scanning electron microscopy (SEM) confirmed that the composite fibers were uniform and the average fiber diameter ranged between 150 nm and 230 nm with an increase in applied potentials from 14 kV to 22 kV. And the transmission electron microscopy (TEM) showed that silver nanoparticles distributed individually in the fibers with the average particle size of about 11 nm. Furthermore, the ultraviolet visible spectrophotometer (UV-vis spectroscopy) test demonstrated that all of Ag⁺ converted to Ag⁰ when the concentration of gelatin was 24 wt% and the mass ratio of GSP to AgNO₃ was about 5:2. The antibacterial activities of the fiber membranes against E.coli and S.aureus were measured via a shake flank test and demonstrated good performance after the importation of silver nanopaticles. Cytotoxicity testing also revealed that fiber membranes contained silver nanoparticles had no cyto-toxic. All the results indicated that the GSP was effective for the formation and stabilization of silver nanoparticles in composite nanofibers mats which had the potential for applications in antimicrobial tissue engineering and wound dressing.     

Mechanical properties of wool fiber in the stretch breaking process

Short wool fibers obtained by the stretch breaking process can be blended with cotton fibers and processed in a cotton spinning system, which has a high production rate. For the structural property of the wool fiber after stretch breaking, the diameter and length of the wool fiber were measured as a function of time. The diameter of the broken fibers was finer than the diameter of untreated fibers. The fiber diameter at the break point was the finest and was more irregular than the original fiber. The broken fiber showed mechanical properties of increased modulus, decreased breaking strain, and increased breaking strength.     

Extraction,Dyeing, and Antibacterial Properties of <Emphasis Type="Italic">Crataegus Elbursensis</Emphasis> Fruit Natural Dye on Wool Yarn

Fruits obtained from shrubs of the Crataegus elbursensis (C. elbursensis) plant demonstrate significant antioxidant and antibacterial properties. In this study, natural dye was sono-extracted from fresh and dried fruits and applied in dyeing and antibacterial finishing of wool. The maximum sono-extraction yield was obtained when optimal conditions of ethanol/ water (4/1 v/v) as extracting solvent, time 30 min, pH 4, temperature 50 oC, and C. elbursensis concentration 10 g/l were used. When wool yarns were dyed with the extracted natural dye, the maximum dye uptake was achieved using dye concentration 75 % owf, and dyeing condition of 100 oC, 60 min, pH 4, and LR 100:1. Different metal salts like aluminum sulfate, copper sulfate, and tin chloride were applied on wool by pre-mordanting method and their effects on dye uptake, color variation, and color fastness were examined. Results showed that the natural dye itself had relatively high uptake and good color fastness on un-mordanted wool. Further, each mordant had different effect on dye uptake, color variation, and color fastness properties depending on its coordination ability with dye molecules and wool chains. Moreover, dyed yarns showed good antibacterial activity against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) bacteria.     

Rheological behavior and spinnability of ethylamine hydroxyethyl chitosan/cellulose co-solution in N-methylmorpholine-N-oxide system

In this work, the novel chitosan derivative ethylamine hydroxyethyl chitosan (EHC) was synthesized and blended with cellulose in an aqueous N-methylmorpholine-N-oxide (NMMO) solution in order to fabricate antibacterial chitosan/cellulose fiber. The rheological behaviors of the obtained co-solution in both steady and dynamic states were carefully investigated to determine the spinnability of the co-solution. In steady state, the addition of EHC was found to preserve the power-law flow characteristics of cellulose in the aqueous NMMO solution, while broadening the first Newtonian fluid-flow area. Under dynamic conditions, both Han-plot and viscoelastic analyses indicated the homogeneity of the co-solution. EHC/cellulose antibacterial fibers were successfully spun via the lyocell process using aqueous NMMO as the solvent, confirming the excellent spinnability of the EHC/cellulose co-solution. Scanning electron microscopy was used to observe the morphology of the obtained EHC/cellulose fibers; they were also investigated for antibacterial activity. The obtained EHC/cellulose fiber exhibited good spinning consistency and strong antibacterial activity against Escherichia coli, demonstrating potential applications for the material in antibacterial textiles.     

Surface characterization of low temperature plasma treated wool fiber

Previous investigation results revealed that after the Low Temperature Plasma (LTP) treatment, the hydrophilicity of wool fiber was improved significantly. Such improvement enhances the wool dyeing and finishing processes which might be due to the changes of the wool surface to a more reactive one. In this paper, wool fibers were treated with LTP with different gases, namely, oxygen, nitrogen and gas mixture (25 % hydrogen/75 % nitrogen). Investigations showed that chemical composition of wool fiber surface varied differently with the different plasma gas used. The surface chemical composition of the different LTP-treated wool fibers was evaluated with different characterization methods, namely FTIR-ATR, XPS and saturated adsorption value. The experimental results were thoroughly discussed.     

Statistical optimization of wool dyeing with Alizarin Red S as a natural dye via central composite design

Recently a revival interest in the use of natural dyes in textile coloration has been growing. The major parts of natural dyes are anthraquinones. Depending on substituents, anthraquinone compounds are dyes, as represented by Alizarin Red S (ARS) which is a major constituent of the natural colorant madder. In this study, colorization of wool fiber by ARS as a natural dye was studied. The progress of the colorization process was followed spectrophotometrically at 500 nm as λ _max. The effective factors on the process were investigated using one factor at a time (OFT) method. Then, the central composite design (CCD) method was applied to design experiments for the evaluation of the interactive effects of the four most important operating variables. The values of the optimized factors for OFT and CCD methods in wool dyeing with ARS were respectively as follow: temperature 70 °C and 55 °C, L/R: 40/1 and 40/2, pH 5.0 and 2.5 and time 60.0 min and 42.0 min. The predicted results by CCD had significantly higher exhaustion percentages and relatively better fastness properties than OFT and were found to be in a good agreement (R²=0.9908) with those obtained by performing experiments. Finally, the obtained results were shown a good wash fastness for dyed wool with ARS.     

Study on the dyeing of wool fabrics with Phytolacca berry natural dyes

Dyeing of wool fabrics with natural dyes from Phytolacca berries has been studied. The effect of dye concentration, dye bath pH, dyeing time and temperature were discussed. The influence of chitosan application on the dyeing properties of wool fabrics was investigated. The SEM photographs of chitosan treated wool fabrics clearly depict the deposition of chitosan on the fibers. The effect of chitosan concentration, dye bath pH, dyeing time and temperature has been studied by orthogonal experiment. It has been proved that the dyed wool samples pretreated by chitosan have higher color fastness, faster dyeing rate, and better antibacterial properties compared with untreated ones.