Synthesis of cationic core-shell fluorine-containing polyacrylate soap-free latex and its application on cotton substrate

Fluorinated polyacrylate latexes are preferably potential materials for use in the textile finishing due to their special surface property and especially economical, low-toxic characteristics compared to fluorinated polyacrylate solutions. A novel cationic fluorine-containing polyacrylate soap-free latex (CFMBD) with core-shell structure was accordingly developed by co-polymerizing dodecafluoroheptyl methacrylate (DFMA), methyl methacrylate (MMA), butyl acrylate (BA), and dimethylaminoethyl methacrylate (DM) using a cationic reactive emulsifier, maleic acid double ester-octadecyl poly(ethyleneoxy)₂₀ ether-ethylene trimethyl ammonium chloride (R303). Then CFMBD was utilized to treat the cotton fabric. Results showed that the as-prepared latex had due structure and its particles had uniform spherical core-shell structure with an average diameter of 125 nm. The core-shell CFMBD latex film thus had two T _g and its thermal property was improved due to the introduction of DFMA. CFMBD could form a smooth resin film on the treated fabric/fiber surface under FESEM observation. XPS analysis indicated the fluoroalkyl groups had the tendency to enrich at the film-air interface. Hydrophobicity of the CFMBD treated fabric was slightly superior to that of the fabric treated by general emulsion but their oleophobicity was identical. Contact angles of water and diiodomethane on the CFMBD treated fabric surface could attain 133.5 ° and 105.5 °, respectively. However, washing durability of the treated fabric by CFMBD showed improvement compared to the general emulsion. In addition, CFMBD didn’t influence whiteness of the treated fabric but would make it slightly stiff at high doses.     

Bioinspired Fabric with Superhydrophilicity and Superoleophobicity for Efficient Oil/Water Separation

The cotton fabric was modified with dopamine methacrylamide (DMA) based on mussel-inspired reaction and polymerized with zwitterionic sulfobetaine methacrylate (SBMA) through free radical polymerization reaction. The poly(DMA-SBMA) contained not only key chemical constituents of dopamine hydrochloride, which strongly adsorbed to fabric substrates, but also hydrophilic groups, providing a hydrophilic surface for fabric due to its strong interaction with water via electrostatic interactions. The chemical structure, surface topography, and surface wettability of the fabric were characterized by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and contact angle experiments, respectively. The results showed that the water contact angle (WCA) of the treated fabric was ~0 °, whereas the underwater oil contact angle (OCA) was ~161 °, as compared to ~25 ° for the control one. It is expected that as-prepared fabrics could be applied in oil/water separation due to such special superhydrophilicity and superoleophobicity.     

Facile fabrication of superhydrophobic cotton fabric from stearyl methacrylate modified polysiloxane/silica nanocomposite

The stearyl methacrylate modified polysiloxane/nanocomposite was synthesized by graft copolymerization between stearyl methacrylate modified polysiloxane with pendent epoxy groups and amino-functionalized nano silica. Then it was utilized to fabricate the superhydrophobic cotton fabric by one-step method. The structures, chemical compositions, thermal properties, surface morphology and wettability were characterized by Fourier Transform Infrared Spectrum (FT-IR), X-ray photoelectron spectroscopy (XPS), Thermo-gravimetric analyzer (TGA), Scanning electron microscopy (SEM) and Static contact angle analyzer. Results showed that a hydrophobic polysiloxane film and many nano-scaled tubercles were coated on the surface of the treated cotton fabrics plus their inherent microscaled roughness, which were the reasons why cotton fabric changed from hydrophilicity to hydrophobicity. In addition, with increase of the amount of nanocomposite, hydrophobicity of the treated cotton fabric would be enhanced; water contact angle of this fabric could attain 157°, which was higher than 141.5° reached by the fabric treated with stearyl methacrylate modified polysiloxane. The superhydrophobic cotton fabric also possessed favorable washing durability. On the other hand, its air permeability, color and softness would not be influenced instead.     

Synthesis,film morphology and performance of novel crosslinked polysiloxane with end-capped epoxy groups on cotton substrates

An epoxy group-terminated polyvinylmethylsiloxane (EPVMS) was firstly prepared via the cohydrolysis/condensation reaction of octamethylcyclotetrasiloxane (D₄), 2,4,6,8-Tetramethyl-2,4,6,8-tetravinylcyclotetrasiloxane (D₄V), and epoxy group-terminated polydimethylsiloxane (ETP) under a base catalyst. Then, the EPVMS was reacted with polymethylhydrosiloxane oligomer (PHMS) by hydrosilylation to develop novel crosslinked polysiloxane with end-capped epoxy groups (CLPS). The chemical structure and the thermal property of the as-prepared products were characterized by Fourier transform infrared spectroscopy (FT-IR), nuclear magnetic resonance spectra (¹H/¹³C NMR) and thermogravimetric analysis (TGA). Finally, the CLPS was applied as the finishing agent to treat the cotton fabrics. The film morphology and the surface properties were examined with scanning electron microscopy (SEM), atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS), contact angle measurements, and other instruments. FT-IR and NMR results confirmed the structure of the resultants. The crosslinked polysiloxane CLPS showed better thermal stability than the uncrosslinked polysiloxane EPVMS. The CLPS film on cotton fabric surface seemed to be smooth compared to the control by SEM. However, owing to the crosslinked structure, the CLPS film on silicon-wafer was inhomogeneous and had a few weak or strong peaks. At 5 nm data scale and in 2×2 μm² scanning field, the root mean square roughness of CLPS film reached to 0.414 nm. XPS analysis further demonstrates that there was a CLPS film covered on the cotton surface. Hydrophobicity of the CLPS treated fabric was superior to that of the EPVMS treated one. Whiteness of the treated fabrics by CLPS and EPVMS did not change at all compared to the control. The softness of the two treated fabrics was both better than that of control and particularly the softness of the EPVMS treated fabrics was preferable. The CLPS treated fabric possessed good washing durability.     

Fluorosilicone modified polyacrylate emulsifier-free latex: Synthesis,properties, and application in fabric finishing

Fluorosilicone modified polyacrylate emulsion was successfully synthesized via emulsifier-free emulsion polymerization using polymerizable surfactant and sol-gel process. TEM analysis indicated that the hybrid particles were spherical-like particles with narrow size distributions. The influence of synthetic conditions on the physical and chemical properties of fluorosilicone modified polyacrylate was investigated, including the mass ratio of methyl methacrylate (MMA)/butyl acrylate (BA) and the content of dodecafluoroheptyl methacrylate (DFMA) and ethyl silicate (TEOS). The water absorption decreased as the MMA/BA mass ratio was reduced from 5/4 to 2/4, then increased afterwards. With the reducing of MMA/BA mass ratio, the tensile strength decreased, while the elongation at break increased. The thermal stability of the hybrid film was improved with the increasing of TEOS amount. Finally, the contact angle results showed that the finished fabric had the excellent water repellency. Meanwhile, the SEM measurements confirmed that the finished fabric had the rough surface. XPS analysis demonstrated that there was a layer of fluorosilicone modified polyacrylate film covered on the finished fabric surface, and fluorinated segments had the tendency to be enriched at the film-air interface.     

Simultaneous synthesis of nano ZnO and surface modification of polyester fabric

In this study, synthesis of zinc oxide nanoparticles was carried out along with the hydrolysis of polyester fabric using sodium hydroxide to increase the surface activity and enhance the nanoparticles adsorption. The polyester fabrics were treated with zinc acetate and sodium hydroxide at different bath conditions, ultrasound and stirrer, resulting in formation of ZnO nanospheres and ZnO nanorods. The presence of zinc oxide with different shapes on the surface of the polyester fabrics was confirmed by scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS). Also, the X-ray diffraction patterns established the composition of wurtzite structure of zinc oxide. The self-cleaning property of treated polyester fabrics was evaluated through discoloring dye stain under sunlight irradiation. The antibacterial activities of the samples against two common pathogenic bacteria including Escherichia coli and Staphylococcus aureus were also assessed. The results indicated that the photocatalytic and antibacterial activities of the ultrasound treated polyester fabrics were superior compared to the stirrer treated samples.     

Synthesis of a dodecylphenylsiloxane oligomer resin/silica nanocomposite and its application to cotton fabrics

A novel dodecylphenylsiloxane oligomer resin/nanocomposite (PHDESR-SiO₂) was prepared by graft copolymerization between dodecyl modified phenylsiloxane resin with pendent epoxy groups (PHDESR) and amino-functionalized silica nanoparticles (BTEPA-SiO₂). PHDESR-SiO₂ was then used to prepare a super hydrophobic surface on cotton fabric by a facile solution-immersion process method. Chemical structures, chemical compositions, wettability, surface morphology, and thermal properties were investigated by Fourier Transform Infrared Spectrum (FT-IR), ¹H-NMR spectrum, X-ray photoelectron spectroscopy (XPS), static contact angle analyzer, scanning electron microscopy (SEM), Particle size distribution (PSD) and thermo-gravimetric analysis (TGA). The results showed that the target product PHDESR-SiO₂ has an anticipative structure with many micro/nanostructure tubercles, a cross-linked network hydrophobic organosilicon resin film and many clusters of cylindrical dodecyl molecular brushes. This created super hydrophobic structure on the surface of the treated cotton fabrics. XPS analysis indicated that the long carbon chain groups had a slight tendency to enrich the film-air interface. In addition, PHDESR-SiO₂ can provide good hydrophobicity for the treated fabric. As the dose of PHDESR-SiO₂ increased, the hydrophobicity of the treated fabric enhanced and consequently the water static contact angle reached 152.5 °. This had little influence on the softness, color, and gas permeability of the fabrics. This makes it slightly stiff at high doses, and the super-hydrophobic cotton fabric also had good launderability.     

Antimicrobial treatment properties of Tencel Jacquard fabrics treated with ginkgo biloba extract and silicon softener

Tencel Jacquard fabric is one of the eco-fabrics used for underwear, sportswear, bedclothes, clothes for aged people, and hospital textiles. It is popular for these uses because it is easy to process into yarns and fabrics alone or in blends, very stable in washing and drying, thermally stable, and easy to dye with deep vibrant colors using direct, reactive, or vat dyes. In order to provide antimicrobial properties for Tencel Jacquard fabrics, they were treated with ginkgo biloba extract and silicon softener using two different processes so the results could be compared. One of the processes treated the fabrics with ginkgo biloba extract and silicon softener simultaneously, and the other process treated the fabrics with these agents sequentially. The treated Tencel Jacquard fabrics were characterized by scanning electron microscopy, and their antimicrobial properties were evaluated. In addition, water repellency, air permeability, water vapor permeability, and yellowness were measured. It was observed that the ginkgo biloba extract and silicon softener were present on the surface of the treated fibers, and the quantity of these agents before and after laundering was proportional to the measured antimicrobial activity of the fabrics before and after laundering. Fabrics treated with both agents had stronger water/oil repellency than fabrics treated with only ginkgo biloba extract. As the quantities of the two treating agents on fabrics were increased, their air permeability and water vapor permeability decreased. No significant changes were observed for yellowness based on the amounts of treating agents applied. From these results, it is expected that Tencel fabrics treated with ginkgo biloba extract and silicon softener are excellent for use as bedclothes.     

Synthesis and Characterization of Waterborne Polyurethane Modified by Acrylate/nano-ZnO for Dyeing of Cotton Fabrics

Waterborne polyurethane modified by acrylate/nano-ZnO (PUA/ZnO) was synthesized and used to improve the wet rubbing fastness of reactive dyed cotton fabric. The reaction conditions were optimized and the products were characterized by FT-IR, TG, DSC, SEM, and particle size distribution. The dyed cotton fabrics were finished with PUA/ZnO emulsion and the rubbing fastness, ultraviolet resistant property, and wearability of treated fabrics were measured. The wet rubbing fastness of treated fabrics was increased by about 0.5–1 rate to achieve 3–4 rate, and the ultraviolet protection factor (UPF) achieved 50+ level. The whiteness, air permeability, and elongation at break of treated fabric were not decreased significantly. SEM showed that the smooth and reticular coating on the surface of treated fabric reduced the mechanical friction force between dyed fabric and rubbing cloth, and thus improved the rubbing fastness. The decomposition temperature of finished fabric was increased by 50–80 °C.     

Highly flame retardancy of cotton fabrics with a novel phosphorus/nitrogen/silicon flame-retardant treating system

A novel reactive flame retardant (FR) containing phosphorus, nitrogen, and silicon was synthesized successfully, and its chemical structure was fully characterized by Fourier transform infrared spectrometry and nuclear magnetic resonance spectrometry (¹H-NMR and ³¹P-NMR). Then it was used to impart flame resistance to cotton fabrics. Vertical flammability and limiting oxygen index test were used to evaluate the flame retardancy of the cotton fabrics treated with FR. When the cotton treated with 150 g/l FR and 50 g/l sodium hypophosphite, the finished cotton can pass the vertical flammability test. Thermogravimetry (TG) was used to evaluate thermal behavior of FR and cotton fabrics. TG results demonstrated that the FR has good thermostability and char-forming ability. After treatment with FR, the thermal stability of the cotton fabrics was clearly improved, indicating that the FR can protect cotton fabric from fire to a certain degree. Furthermore, attenuated total reflection Fourier transform infrared spectroscopy was utilized to characterize the chemical structure of FR treated cotton fabrics. Finally, the surface morphology in different regions of the treated cotton was observed using scanning electron microscopy.     

Synthesis and characterization of hybrid latexes from soybean oil-based polyurethane and poly(2,2,2-trifluoroethyl methacrylate)

A class of novel fluorine containing core-shell hybrid latexes were obtained from soybean oil-based polyurethanes and poly(2,2,2-trifluoroethyl methacrylate) (PTFEMA) by two-step synthesis under mild reaction conditions. Structural and morphology properties of the resulting hybrid latexs have been characterized by FT-IR and TEM. In addition, thermal properties (DSC, TGA) and coating performance (contact angle, stress-strain curve, and surface free energy) were investigated and discussed. The hybrid latexes exhibit outstanding thermal stability and coating performance. More importantly, through this method, low-valued foods are successfully transformed into high-valued functional materials which bring new solutions for preparing materials from renewable sources.     

Assessment of the surface roughness of cotton fabrics through different yarn and fabric structural properties

The effects of some yarn properties (i.e. type, count, twist level, ply number, unevenness and crimp) and fabric constructional properties (i.e. cover, thickness and balance) on surface roughness values of cotton woven fabrics were investigated. A general overview of the results showed that surface roughness values of fabrics were affected from yarn and fabric properties and the effects were related to fabric balance, fabric cover (not cover factor), fabric thickness and crimp values of yarns in fabric structures. Surface roughness values of fabrics decreased as yarn fineness and yarn twist levels increased but as yarn ply number decreased. Also, surface roughness values gradually decreased from open-end yarn constituting fabrics to combed yarn constituting fabrics. Results showed that different properties of yarns caused changes in yarn crimps in fabric structure and also governed the changes in fabric balance, as well as changes in roughness of fabric surfaces. The changing properties of yarns and impact of these properties on fabric construction affected the formation of cotton fabric surfaces from smooth to coarse.     

Effect of Silver Particle size on color and Antibacterial properties of silk and cotton Fabrics

In this study silver nanoparticles with different particle sizes and hence colors were synthesized on silk and cotton fabrics through reduction of silver nitrate. Particle sizes of the silver colloids were measured by dynamic light scattering (DLS). The structure and properties of the treated fabrics were characterized by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD), and UV-Vis reflectance spectroscopy. Various characteristics of the treated fabrics including antibacterial activities against a Gram positive (Staphylococcus aureus) and a Gram negative (Escherichia coli) bacteria, color effect, wash and light fastness, water absorption, fabric rigidity, and UV blocking properties were also assessed. The results indicated that the treated fabrics displayed different colors in the presence of silver nanoparticles with different particle sizes and exhibited good and durable fastness properties. Also, the size of the silver particles had a tangible effect on antibacterial activity of treated fabrics and its antibacterial performance was improved by decreasing the size of particles. Moreover, this process imparted significantly UV blocking activity to fabric samples.     

Improving certain properties of wool fibers by applying chitosan nanoparticles and atmospheric plasma treatment

The nanochitosan particles were prepared by ionic gelation method using sodium tripolyphosphate (TPP) as anionic chemical agent. Structural and morphological properties of the nanoparticles were characterized by dynamic light scattering (DLS), transmission electron microscopy (TEM), and Fourier transform infrared spectroscopy (FTIR) analyses. The results showed that nanoparticles were spherical with a diameter range of 17-105 nm. After nanochitosan synthesis, the effects of chitosan and nanochitosan concentrations on the dyeability, fastness properties, shrink-proofing, tensile strengths, and surface friction coefficients of untreated and plasma treated wool fabrics were investigated. The studies revealed that nanochitosan treated wool fabric possesses better dyeing and shrink-proofing properties in comparison with conventional chitosan treated fabrics.     

Effects of NCO/OH ratios and polyols during polymerization of water-based polyurethanes on polyurethane modified polylactide fabrics

Polylactides (PLAs) are a type of environmental friendly material. PLA fabrics feature excellent performance in terms of texture, comfort, curling effect, crystallinity, and transparency. However, because of its aliphatic polyester structure, PLA is relatively fragile as compared with the commercially available products like PET or Nylon. This study adopted water-based polyurethane (PU) to modify the surface of PLA fabrics, thereby enhancing the fabrics’ mechanical properties. Various polyols such as polytetrahydrofuran (PTMG), polycaprolactone diol (PCL), and polycarbonates diol (PC) were used and various NCO/OH molar ratios were designed in this study. As the PLA fabric was processed by dipping in various PU dispersions, it was found that the breaking strength of the fabric was increased, while its elongation at breakage decreased. Particularly, the breaking strength of the fabric modified by PUD50PC containing 50 weight percent of PC and two other polyols was the most prominent showing an 80 % increase in strength. Furthermore, the abrasion resistance of the PUD50PC-modified PLA fabric showed a roughly 6 times increase as compared to the plain PLA fabric. SEM images also reveal that after processing with water-based PU, the PLA fibers are bonded tightly with the water-based PU molecules to increase the breaking strength of the PLA fabrics.     

A new consolidation system for aged silk fabrics: Interaction between ethylene glycol diglycidyl ether,silk Fibroin and Artificial Aged Silk Fabrics

Consolidation of fragile historic silks is of great importance for further displays and researches. An effective and convenient method to consolidate aged silk fabric has been proposed by using a silk fibroin (SF)/ethylene glycol diglycidyl ether (EGDE) consolidation system. Artificial aged silk fabrics treated with SF/EGDE show great improvement in mechanical properties. The chemical reaction between EGDE and silk fabrics has been proved in previous paper. And in this paper, mechanical test, field emission scanning electron microscopy (FESEM), Fourier transform infrared spectrum (FTIR) test and amino acid analysis (AAA) were applied to illustrate the interactions between SF and silk fabric, EGDE and SF. Results show that SF takes part in the consolidation in the form of adhesions on the surface of silk fibers. The chemical reactions and film adhesion are both responsible for the improvements of mechanical properties in the consolidation.     

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.     

Polyester modification through synthesis of copper nanoparticles in presence of triethanolamine optimized with response surface methodology

In this paper, polyester fabric was modified through synthesis and fabrication of Cu/Cu₂O nanoparticles using a facile and cost-effective method at boil by chemical reduction through exhaustion route. Triethanolamine (TEA) was used for aminolysis of polyester fabric and pH adjusting, copper sulfate (CuSO₄) as metal salt, sodium hypophosphite (SHP) as reducing agent and polyvinylpyrrolidone (PVP) as stabilizer. A response surface methodology was also employed to optimize the reaction conditions and study the effects of SHP, PVP and TEA concentrations in the processing. The images of field-emission scanning electron microscopy (FESEM), the patterns of energy-dispersive spectroscopy (EDX) and X-ray diffraction (XRD) patterns confirmed successfully synthesis of Cu and Cu₂O nanoparticles on the polyester fabric. Further, the thermal behavior of the untreated and treated fabrics was studied by using thermogravimetric analysis (TGA) and differential scanning colorimetry (DSC). The treated fabrics indicated good properties regarding wettability and flame-retardant along with high tensile strength.     

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.     

Highly Durable and Robust Superhydrophobic/Superoleophilic Cotton Fabric with Well-designed Roughness for Oil/Water Separation

Herein we report a simple and reproducible method for fabricating highly durable and robust superhydrophobic and superoleophilic cotton fabrics via simultaneous radiation-induced graft polymerization of glycidyl methacrylate and subsequent chemical modifications with aminopropyltriethoxysilane and hexamethyldisilazane. The chemical structure and the surface topography of the pristine and the modified cotton fabrics were investigated in detail by ATR-FTIR, XPS, and ²⁹Si NMR, and a grafting layer was successfully immobilized onto the surface of the cotton fabric by forming covalent bonds. Multi-dimensional surface roughness was created by combining micro-sized fibers of the cotton fabric, nanoscaled protuberances of the grafting chain, and molecular level spherical projection points of silicon methyl. The superhydrophobic cotton fabric exhibited long-term stability, ultra-high durability and robustness, and maintained its properties even after 25 wash cycles. The fabric also showed excellent water repellency with a water contact angle of 153 ° and a high efficiency of oil/water separation (98 %). The superhydrophobic/superoleophilic cotton fabric developed in the present work exhibits important potential applications in superhydrophobic textiles and oil/water separation.