Preparation of the cotton fabric with ultraviolet resistance and antibacterial activity using nano attapulgite colloidal particles

A carefully designed surface modification technique for the preparation of multifunctional cotton fabric was successfully developed by the functionalization of cotton fabric with nano attapulgite (ATP) colloidal particles. The dispersion of the nano ATP colloidal particles, the morphology, microstructure, thermal stability, ultraviolet resistance, antibacterial activity and air permeability of the treated cotton fabric were characterized. The results showed that the particle size of the ATP particle distributed between 100 nm to 150 nm after dispersion. The SEM (scanning electron microscopy) and FTIR (Fourier transform infrared spectra) analysis demonstrated that the ATP particles were successfully introduced to surface of the cotton fabric. The structural and thermal stability of the treated fabric were higher than those of the untreated fabric. The ATP treated cotton fabric possessed excellent ultraviolet resistance and antibacterial activity. Furthermore, the treatment did not affect the wear ability of the cotton fabric. The multifunctional cotton fabric meets the market demand for natural products.     

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.     

Preparation and characterization of (POSS/TiO2)n multi-coatings based on PBO fiber surface for improvement of UV resistance

The application of poly (p-phenylene-2, 6-benzobisoxazole) (PBO) fiber as reinforcement in composite material was restricted by its photo-degradation, therefore, some measures should be considered to protect PBO fiber against UV aging. In this study, A series of multilayer coating for (POSS/TiO₂)_n was prepared on PBO fiber surface via LbL assembly technique for enhancement of UV resistance. TiO₂ as UV absorbing material was used to relieve UV-degradation of PBO. Surface elemental composition, surface morphology, mechanical and interfacial properties, and UV resistance of uncoated and coated PBO fibers were investigated. These experimental results show multilayer coating of (POSS/TiO₂)_n was uniform deposition on fiber surface after treatment, tensile strength decreased to certain extent, interfacial shear strength increased in a small range and UV resistance is obvious enhanced. After the same accelerated aging time under UV irradiation, the retention of tensile strength and intrinsic viscosity of coated PBO fibers were much better than that of untreated PBO fibers.     

Preparation and property evaluation of sound-absorbing/thermal-insulating PU composite boards with cushion protection

This study used recycled fibers and inflaming retarding fibers to form composite nonwoven and then compounded with PU foam preparing composite board with sound-absorbing, thermal-insulating and cushion properties. Effects of foam density and composite nonwoven on three properties of PU composite board have studied. Result shows that, with increase of foam density, composite boards had higher sound absorbing coefficient at medium and high frequencies, lower thermal insulation as well as firstly improved and then decreased cushion property. After assessment, the optimal foam density was 60 kg/m³. For diverse requirements, PU foam matches with different kinds of composite nonwoven to achieve excellent cushion property. The resulting composite board can effectively ease hurts from rigid wall, and could be applied in kindergarten, music hall, audio-visual room, pub and recreational centre etc in the future.     

Immobilization of TiO2 nanoparticles on PET fabric modified with silane coupling agent by low temperature hydrothermal method

PET fabric was first modified with silane coupling agent KH-560, and then was loaded with a layer of nano-scaled TiO₂ particles using tetrabutyl titanate as precursor by low temperature hydrothermal method, followed by dyeing with Disperse Blue 56. The morphology, crystalline phase, chemical modification, thermal stability and optical property of PET fiber before and after treatments were studied by scanning electron microscope, X-ray diffraction, X-ray photoelectron spectroscopy, thermal gravimetric and diffuse reflectance spectrum techniques. The properties of tensile, air permeability, luster, ultraviolet (UV) protection, photocatalytic activity, K/S value and color fastness were also measured. It was found that compared with the TiO₂-coated fabric without modification with KH-560, the loading of TiO₂ nanoparticles on the surface of the TiO₂-coated fabric modified with KH-560 was obviously improved. The pure anatase TiO₂ nanoparticle was grafted onto the fiber surface. The onset decomposition temperature increased. The absorbing capability to ultraviolet radiation was enhanced. The properties of tensile, air permeability, luster, K/S value and color fastness changed slightly. The UV protection ability and photodegradation of methyl orange under UV illumination were enhanced to some extent.     

Preparation of poly(acrylonitrile)-grafted silk fibers with antibacterial properties

This study is focused on investigating the feasibility of using silver(I) ions loaded poly(acrylonitrile)-grafted silk fibers as antibacterial dressing material. The optimum grafting conditions for ceric ammonium nitrate induced graft-copolymerization of acrylonitrile onto silk fibers were found to include initiator concentration of 35 mM, catalyst HNO₃ concentration of 0.40 M and initiation time of 10 min. The poly(acrylonitrile)-grafted silk fibers were loaded with silver(I) ions by equilibration method. The resulting fibers were investigated for their biocidal action against E. coli, by using zone inhibition and colonies counting method.     

Preparation and properties of 2-(2-aminoethoxy) ethyl chitosan/cellulose fiber using N-methylmorpholine-N-oxide process

N-methylmorpholine-N-oxide (NMMO) is used widely in the manufacturing of man-made cellulose fibers and functional lyocell fibers due to its environment-friendly advantage. Although chitosan is known as a natural antibacterial polymer it has poor solubility in neutral to basic medium and the antibacterial activity is shown only in acidic medium. Chitosan’s poor solubility in NMMO is the disadvantage for the production of antibacterial lyocell fibers. This paper investigates a more “NMMO soluble” derivative of chitosan, 2-(2-aminoethoxy) ethyl chitosan (AECS). AECS has greatly improved solubility in NMMO hydrate, and stronger antibacterial activity than chitosan. AECS was introduced to modify the lyocell fiber spun in a co-solution of cellulose and AECS in NMMO hydrate. The physical properties and antibacterial activity of the fibers were examined and the results indicated that the modified lyocell fiber, containing more than 2 wt% of AECS, exhibits good antibacterial activity against E. coli and slightly decreased tensile strength compared with unmodified fibers.     

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.     

Multifunctional melt-mixed Ag/TiO2 nanocomposite PP fabrics: Water vapour permeability, UV resistance, UV protection and wear properties

This research deals with the investigating the effect of nanoparticles on the various properties of nanocomposite fabrics produced from melt spinning of various blend ratios of prepared masterbatch containing Ag/TiO₂ nanoparticles. The results revealed that the wear properties of modified fabrics improved as compared to pure fabrics with a trend justified considering modulus or crystallinity of fabrics with opposite effects. About 40 % UV protection enhancement has been obtained applying this kind of nanoparticles in the close relationship with the crimp contraction of textured yarns. A considerable improvement in the garment comfort has been recorded for nanocomposite sample containing 1 wt% nanoparticles. The lower permeability at low environment temperature and a higher at higher one, as compared to the pure sample, were obtained using this sample. It is highly interesting that these desirable changes in permeability can be achieved in the range of common environment temperatures (15–35 °C) being adapted to the human body requirements. The changing point is about 25 °C exactly meeting the body requirements by changing environment temperatures. A UV-induced solid state nanocomposite interaction increasing wear properties of UV-irradiated nanocomposite fabrics has been discovered.     

Preparation and properties of antibacterial Poly(vinyl alcohol) nanofibers by nanoparticles

Poly(vinyl alcohol) (PVA)/Ag-zeolite nanofiber webs were prepared with different concentrations of Ag-zeolite nanoparticles by the electrospinning technique. Scanning electron microscopy (SEM), energy-dispersive X-ray spectrometry (EDS), transmission electron microscopy (TEM), Fourier transform-infrared (FT-IR) spectroscopy, thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), Instron, and antibacterial activities analysis were utilized to characterize the morphology and properties of the PVA/Ag-zeolite nanofiber webs. The study results showed that the polymer concentration, applied voltages and tip-to-collector distances were the main factors influencing the morphology of the electrospun nanofiber webs. The introduction of Ag-zeolite nanoparticles improved the mechanical properties and thermal stability of the PVA nanofiber webs. TEM data demonstrated that the Ag-zeolite nanoparticles were well distributed within the nanofiber. FTIR revealed a possible interaction between the PVA matrix and the Ag-zeolite nanoparticles. These fibers showed an antibacterial efficacy of 99.8 % and over against Staphylococcus aureus and Klebsiella pneumoniae at Ag-zeolite concentrations of 1 % and over, because of the presence of the silver nanoparticles in the zeolite.     

Preparation of silk sericin beads using LiCl/DMSO solvent and their potential as a drug carrier for oral administration

Silk sericin (SS) was fabricated into beads using LiCl/DMSO solution as a solvent. Up to 30 % (w/v) of SS could be dissolved within 3 hours, and the shape of solidified SS depends on the concentration of SS. Ethanol was the best coagulant among alcohols, making beads with suitable mechanical strength for further application. SS beads swell more at a pH above the isoelectric point (pl) than below the pl. The pH and the presence of an enzyme greatly affect the dissolution rate of SS beads. Whereas only 10 % of SS beads were dissolved at pH 2.2 in the presence of pepsin, more than 45 % of SS beads were dissolved at pH 7.4 in the presence of trypsin. The release of drug was suppressed in a stomach-like environment while promoted in an intestine-like environment.     

A study of hybrid organic/inorganic hydrogel films based on in situ-generated TiO2 nanoparticles and methacrylated gelatin

Methacrylated gelatin films with in situ-generated TiO₂ nanoparticles containing varying weight percentages of gelatin (0 %, 0.5 %, 1 %, 2 % and 4 %) were successfully prepared as novel biomaterials. ¹H-NMR spectroscopy confirmed their methacrylation with a 79 % degree of substitution. TiO₂ nanoparticles were uniformly distributed in the films with the average particle size increasing from 85 to 130 nm in proportion to an increase in TiO₂ concentration from 0.5 to 4 wt%. The water absorption of various gelatin methacrylamide/TiO₂ films was in the range of 471–758 %, which was enough to prevent wound beds from exudates accumulation. And in vitro degradation test in PBS showed that the three-dimensional structure of all samples basically remained unchanged although more than or nearly half the mass of specimens decreased after 4 weeks’ degradation, and the pH levels of all sample solutions were maintained in an adequate range of 6.5–7.4 for cell and tissue growth during the whole process. The antibacterial activities of the films against E. coli and S. aureus were measured via a shake flask test and demonstrated good performance after the importation of TiO₂ nanoparticles. Cytotoxicity testing revealed that all films had no cytotoxicity and showed favorable adherence in the presence of L929 cells. The results suggest that hybrid hydrogel films hold potential for antibacterial wound dressing and tissue engineering scaffold applications.     

Preparation of monodisperse poly(vinyl alcohol) (PVA) nanoparticles by dispersion polymerization and heterogeneous surface saponification

Monodisperse poly(vinyl alcohol) (PVA)/poly(vinyl acetate) (PVAc) nanoparticles with a skin-core structure were prepared through heterogeneous surface saponification of PVAc nanoparticles. For the preparation of PVAc nanoparticles with a uniform particle size distribution, vinyl acetate (VAc) was dispersion polymerized in a mixed solvent of ethanol and water using PVA with a low degree of saponification as a stabilizer. Increase of the amount of ethanol in media, the resulting PVAc nanoparticle size increases due to increasing solubility of VAc and oligomer PVAc. To preserve the sphericity and size uniformity of PVAc nanoparticles, we restricted saponification to the surface of the nanoparticles by using a small amount of aqueous sodium hydroxide solution. To determine the proper concentration of alkali solution for heterogeneous saponification, monodisperse PVAc nanoparticles were saponified with different concentrations of alkali solution at 25 °C for 0.5–3.0 h. The PVA/PVAc nanoparticles obtained by the heterogeneous saponification with 4 % (relative to the amount of the VAc) alkali solution for 2.0 h were uniformly shaped and monodispersed with diameter ranging from 428 to 615 nm. Transmission electron microscopy (TEM) confirmed the spherical nature and regular skin-core structure of the PVA/PVAc nanoparticles.     

Preparation of poly(vinyl alcohol)/ZrO2 composite nanofibers via co-axial electrospinning with higher ZrO2 particle content

Poly(vinyl alcohol) (PVA)/zirconium oxide (ZrO₂) composite nanofibers with a skin-core structure were prepared and the effect of ZrO₂ particle content on uniform web formation was investigated. The optimized polymer concentration, tip to collector distance, and applied voltage for electrospinning were 11 wt%, 12 cm, and 20 kV, respectively. Skin-core PVA/ZrO₂ composite nanofibers containing up to 12 wt% ZrO₂ were successfully prepared, but it was difficult to obtain PVA/ZrO₂ composite nanofiber webs via conventional electrospinning. Increasing the amount of ZrO₂ caused the morphology of the PVA/ZrO₂ composite nanofibers to become a non-uniform nanoweb with irregular nanofiber diameters. While it was difficult to obtain a uniform nanofiber web containing a content of ZrO₂ over 6 wt% for conventional electrospinning, a more uniform nanofiber web could be obtained at up to 9 wt% ZrO₂ using a skin-core dual nozzle. More uniform webs could also be obtained when ZrO₂ was in the skin rather than the core.     

Preparation and characterization of poly(2-hydroxyethyl methacrylate) grafted bacterial cellulose using atom transfer radical polymerization

The purpose of this study is to synthesize grafted Bacterial Cellulose (BC) nanofibers using Atom Transfer Radical Polymerization (ATRP) reinforced into poly(2-hydroxyethyl methacrylate) (PHEMA) hydrogel matrix. Nanofibers grafting polymerizations were conducted in the presence of the catalyst CuCl/CuBr and the initiator 2-bromoisobutyrylbromide (2-BiBr). Degrees of substitution (DS) of BC-macroinitiators were quantified using both elemental analysis and gravimetric method. FTIR results confirmed BC nanofibers’ surface modifications of both initiator and hydroxyethyl methacrylate (HEMA) grafts. X-ray spectroscopy further confirmed the increase in carbonyl content after PHEMA-grafting polymerization. Results of the gravimetric analysis showed an increase in the weight of the grafted BC upon increasing reaction time. Furthermore, the change in the swelling ratio percentages of the reinforced composites product (BC-MI-3-g-PHEMA-1.5) was considerably higher based on reaction time. Slight increase in the swelling ratio of BC-MI-3 nanofibers was observed after 48 hours to reach 31 %. Moreover, results of thermal gravimetric analysis (TGA) demonstrated that decomposition temperature at 50 % weight loss (T₅₀) decreased to 350 °C for BC-MI-3-g-PHEMA-1.5. These characteristics demonstrate potentials for applications in the biomedical fields including drug delivery and wound care.     

Characterization of Solanum chomatophilum resistance to 2 aphid potato pests, Macrosiphum euphorbiae (Thomas) and Myzus persicae (Sulzer)

The aphids Macrosiphum euphorbiae (Thomas) and Myzus persicae (Sulzer) (Hemiptera: Aphididae) are responsible for yield reduction in potato (Solanum tuberosum) production by direct phloem feeding and by spreading viruses. Breeding resistant traits from Solanum chomatophilum into the potato germplasm provides alternative means to control aphid infestations. Integrated pest management strategy, using plant resistance, benefits from the characterization of the resistance and of its impact on aphid biology. Our objective was to characterize the resistance of S. chomatophilum by assessing the effects of accessions, plant parts on aphid performance, and by assessing the impact of the resistance factors on different aphid developmental stages and on alate morph production. Detailed aphid performance was obtained by measuring fecundity, survival, percentage of nymphs that reached adult moult, and population growth using whole plant and clip cage experimental designs. Accession and plant physiological age, but not aphid developmental stage, influenced all life-history parameters, except for alate morph production which was not induced on the resistant accessions. Plant part influence was independent of plant species and accession. Both experimental designs resulted in congruent resistance levels at the accession level for each of the two aphid species, supporting the use of any of them in S. chomatophilum resistance screening. PI243340 was resistant to both aphid species, while PI365324 and PI310990 were also resistant to M. euphorbiae and M. persicae, respectively.     

Fabrication of homogeneous multi-walled carbon nanotube/poly (vinyl alcohol) composite films using for microwave absorption application

Poly (vinyl alcohol) (PVA)/multi walled carbon nanotubes (MWNT) nanocomposite films were fabricated and their microwave absorption behavior were evaluated using vector network analyzer in the frequency range of 8–12 GHz (Xband). The uniform, stable dispersion and well oriented MWNT within the PVA matrix were achieved through using sodium dodecyl sulfate (SDS) as dispersing agent. The surface morphology of the PVA/SDS/MWNT films was examined by scanning electron microscope (SEM). The SEM analysis of the film samples revealed the uniform appearance in the whole surfaces of the fabricated composite films. However, some roughness on the surface was observed due to the presence of MWNT in the film structure. The PVA/SDS/MWNT films show significant increase in microwave absorption which is improved by increasing the MWNT content. The PVA/SDS/MWNT nanocomposite film sample with MWNT loading of 10 wt% showed the maximum and the relatively high microwave absorption of 28.00 dB at the frequency of 8.6 GHz.     

The effect of casting solvent on the structural characteristics and miscibility of regenerated silk fibroin/Poly(vinyl alcohol) blends

Regenerated silk fibroin(SF)/Poly(vinyl alcohol)[PVA] blend films were prepared using different casting solvents, water and formic acid, to elucidate the effect of casting solvent on the structure and miscibility of SF/PVA blends. FTIR and XRD measurement suggested thatβ-sheet conformation of SF was not changed by addition of PVA in case of formic acid casting and the casting solvent determined the crystallized component of SF/PVA, leading to a different trend in the overall crystallinity between the two blends. The casting solvent had a dominant role in deciding phase behavior and molecular miscibility of blend films. SEM observation and DMTA measurement elucidated that water solvent produced phase-separated blend films while formic acid yielded one phase blend films with partial miscibility in molecular level indicating that the miscibility of SF blend can be improved by choosing a proper co-solvent.     

Organic-inorganic hybrid of chitosan/poly (vinyl alcohol) containing yttrium(III) membrane for the removal of Cr(VI)

In this present study, an organic-inorganic hybrid membrane was prepared by embedding yttrium(III) into chitosan matrix for the removal of Cr(VI) from aqueous solutions. Several techniques, including fourier infrared spectrum (FTIR), scanning electron microscope (SEM), X-ray diffraction (XRD), and transmission electron microscope (TEM) are employed to characterize the properties of the membrane. The mechanical properties of the membrane were also examined. The chitosan/poly(vinyl alcohol) containing yttrium(III) (CY) membrane was experimentally used for the removal of Cr(VI) ions from aqueous solution under the optimized conditions. The results showed that the adsorption capacity for the removal of Cr(VI) ions was enhanced when yttrium(III) was introduced. The adsorption data from the experiment were fit well by Langmuir isotherm. Based on Langmuir model, q _m was calculated to be 38.48 mg g^?1. Kinetic study results indicated that the adsorption process followed a pseudo-second-order kinetics.     

Pervaporation separation of dimethyl carbonate/methanol binary mixtures with poly(vinyl alcohol)-perfluorslulfonic acid/poly(acrylonitrile) hollow fiber composite membranes

Using poly(vinyl alcohol) (PVA) and perfluorslulfonic acid (PFSA) as coating materials, poly(acrylonitrile) (PAN) hollow fiber ultrafiltration membrane as substrate, PVA-PFSA/PAN composite membranes were fabricated by dip-coating method. The fabricated composite membranes were used to the separation of dimethyl carbonate (DMC)/methanol (MeOH) binary mixtures by pervaporation process. SEM images verify that the coated layer is well combined with substrate and the thickness nearly linearly increases with the coating solution concentration. The separation factor increases but at cost of the decline of permeation flux when the concentration of the coating solution or its PVA mass fraction increase. The permeation flux increases and separation factor slightly increases with the feed temperature increasing at 30–60 °C. The increase of feed MeOH concentration leads to an improvement of permeation flux and a decline of separation factor.