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.     

The preparation and characterization of conductive poly(ethylene terephthalate)/polyaniline composite fibers using benzoyl peroxide

Conductive polyaniline (PAn)/poly(ethylene terephthalate) (PET) composite fibers were prepared by chemical polymerization of aniline in the presence of PET fibers using benzoyl peroxide (Bz₂O₂) in organic solvent/aqueous hydrochloric acid mixtures. The effects of polymerization conditions such as organic solvent/water ratio, oxidant, aniline and hydrochloric acid concentrations and temperature were investigated on the amount of PAn deposited on PET fiber and the electrical surface resistance of composite fibers. The maximum PAn content and the lowest electrical surface resistance of composite fibers were observed at HCl concentrations of 0.5 mol L⁻¹. The properties of PAn/PET composite fibers such as density, diameter, tensile strength and breaking elongation were also investigated in comparison with those of pure PET. Characterization of conductive composite fibers was carried out by FTIR, TGA, SEM techniques, surface resistance measurements, and cross section images taken by optical microscope.     

Structure and properties of silk fibroin modified cotton

In this research, a novel cotton fiber with a silk fibroin (SF) coating was prepared by the oxidation of a cotton thread with sodium periodate and subsequent treatment in a solution of silk fibroin. The structures of both the oxidized cotton samples and the SF modified cotton samples were investigated by Fourier transform infrared (FT-IR) in combination with X-ray photoelectron spectroscopy (XPS) analysis. Other performances such as surface morphology and breaking strength were also studied. The results indicated that the weight of the oxidized cotton samples increased during SF treatment, while that of the un-oxidized cotton (pure cotton) samples reduced after SF treatment. Compared with the pure cotton samples, the oxidized cotton clearly showed a characteristic absorption band at 1730 cm⁻¹ due to the stretching vibration of the C=O double bond of the aldehyde group. After being treated with the SF solution, the oxidized cotton fiber showed a weakened characteristic absorption band at 1730 cm⁻¹ and a new absorption band at round 1540 cm⁻¹, suggesting the formation of C-N bond between aldehyde groups in the oxidized cotton and primary amines in the silk fibroin. The results were also confirmed by XPS analysis. Compared with the oxidized cotton samples, the SF treated cottons had relatively smooth surfaces, similar breaking strength, and the improved wrinkle recovery angles. The results in this research suggest that cotton based materials with protein coating can be achieved without using any other crosslinking agents by the method introduced.     

Relationships between antithrombogenicity and surface free energy of regenerated silk fibroin films

Silk fibroin (SF) was dissolved in calcium chloride/ethanol/water mixture (1/2/8 in mole ratio) at 70°C for 4 h. The dissolved silk fibroin was regenerated by casting the dialyzed solution into the films. The films were treated with 50% aqueous solution of methanol for different times, and their antithrombogenicity was evaluated byin vitro andin vivo tests.In vivo blood tests were made by a method of peripheral vein indwelling suture. It was found that the silk fibroin had a good anti-thrombogenicity and an absorbability even though the polymer showed foreign body reaction. Finally, the blood compatibilty of silk fibroin films which were subjected to structural change by the methanol treatment, was examined in connection with their interfacial surface energy, and a correlation between these properties was found to be present.     

Surface modifications of natural Kanchipuram silk (pattu) fibers using glow discharge air Plasma

Experimental investigations have been carried out to modify the surface properties of natural Kanchipuram silk (pattu) fibers using a low temperature DC glow discharge air Plasma. Silk is an externally spun fibrous protein secretion formed into fibers. Plasma treatment is an eco-friendly, dry, and clean process over wet chemical method and does not suffer from any environmental and health concerns. Experiments have been performed considering three parameters such as discharge current, treatment time, and working pressure. The structural, thermal, morphological, optical, and mechanical studies of raw and plasma treated silk fibers have been obtained out using attenuated total reflection-Fourier transform infrared spectroscopy (ATR-FTIR) spectroscopy, X-ray diffraction (XRD), thermo gravimetric analyzer (TGA), scanning electron microscope (SEM) with energy dispersive spectroscopy (EDS), diffuse absorbance spectroscopy, and tensile test. A comparative study has been done for the untreated and different treated fibers. Various characterization analyses reveal that surface roughness of the plasma treated silk fiber is increased and also crystallite size of treated samples is enhanced, plasma treated silk fibers maintain the whiteness effect and it is observed that UV transmittance region (A & B) is more for the treated fiber which signifies enhanced UV protection.     

Frictional and tensile properties of conducting polymer coated wool and alpaca fibers

Wool and alpaca fibers were coated with polypyrrole by vapor-phase polymerisation method. The changes in frictional and tensile properties of the single fibers upon coating with the conductive polymer are presented. Coating a thin layer of polypyrrole on the alpaca and wool fibers results in a significant reduction in the fiber coefficient of friction, as the conducting polymer layer smooths the protruding edges of the fiber scales. It also reduces the directional friction effect of the fibers. Depending on the type of fiber, the coating may slightly enhance the tensile properties of the coated fibers.     

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.     

Structure and performance of<Emphasis Type="Italic">Bombyx mori</Emphasis> silk modified with nano-TiO<Subscript>2</Subscript> and chitosan

Bombyx mori (B. mori) silk was modified with the nano-TiO₂ and chitosan dispersion system by the crosslinking reactions of citric acid (CA) and maleic anhydride (MA). The average size of the nano-TiO₂ particles in the aqueous dispersion system was 36.7 nm. The scanning electron microscopy (SEM) micrographs showed that the nano-TiO₂ particles were spherical and homogeneously dispersed in the dispersion system, and the surface ofB. mori silk fiber treated with the nano-TiO₂ and chitosan dispersion system was rougher than that of the untreated one. X-ray diffraction (XRD) and Fourier transform infrared (FT-IR) Spectrometry indicated that the crystallinity of theB. mori silk fiber increased after treatment. It was also found that the nano-TiO₂ and chitosan contributed to significantly enhance the mechanical properties including breaking strength, breaking elongation, initial modulus, rupture work, and elastic recovery property of theB. mori silk fiber. The wrinkle-resistant performance of the treatedB. mori silk fabrics was also greatly improved.     

Dyeing and fastness properties of a reactive disperse dye on PET, nylon, silk and N/P fabrics

Dyeing and color fastness properties of a reactive disperse dye containing an acetoxyethylsulphone group on PET, Nylon, silk and N/P fabrics were examined. The reactive disperse dye exhibited almost the same dyeing properties on PET fabric as a conventional disperse dye except the level of dye uptake. The most appropriate pH and dyeing temperature for the dyeing of Nylon fabric were 7 and 100°C respectively. The build-up on Nylon fabric was good and various color fastnesses were good to excellent due to the formation of the covalent bond. Application of the reactive disperse dye on silk fabric at pH 9 and 80°C yielded optimum color strength. The rate of dyeing on Nylon fabric was faster than that on PET fabric when both fabrics were dyed simultaneously in a dye bath, accordingly color strength of the dyed Nylon was higher. The reactive disperse dye can be applied for one-step and one-bath dyeing of N/P mixture fabric with good color fastness.     

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.     

Sonicator dyeing of modified cotton, wool and silk with Mahonia napaulensis DC. and identification of the colorant in Mahonia

Mahonia napaulensis DC. (local name—Taming) family Berberidaceae, produces natural dye from its stem which has been used for dyeing textiles by the Apatanis (a tribe of Arunachal Pradesh) since ancient times. Sonicator dyeing with Mahonia napaulensis showed marked improvement in dye uptake. It showed that pretreatment with metal mordant (2%, w/w with respect to the fabric) improved substantially the fastness properties for dyed cotton, silk fabrics and wool yarn. Five fractions were isolated from column chromatography of the stem extract of Mahonia. Attempts have been made to identify these fractions by matching the spectral data which indicated that they were from a well-known isoquinoline alkaloid family.     

Mechanical properties and crystal structure transition of biodegradable poly(butylene succinate-co-terephthalate) (PBST) fibers

Mechanical properties of biodegradable poly(butylene succinate-co-terephthalate) (PBST) fibers with 70 mol% butylene terephthalate (BT) were intensively investigated. Chemical structure composed of hard BT units and soft butylene succinate (BS) units made contributions to the higher elongation at break and lower initial modulus of PBST fibers than poly(butylene terephthalate) (PBT) fibers. Moreover, PBST fibers had better elastic properties than PBT fibers by exploring their elastic recovery. The stretch elastic recovery mechanism of PBST fibers was clarified from the point of crystal structure transition. According to the preliminary studies by wide angle X-ray diffraction (WAXD) measurements, two polymorphs (α form and β form) were confirmed when PBST fibers were applied to different deformations. With the help of intensive study by small angle X-ray scattering (SAXS) measurements, the crystal structure transition of PBST fibers was further verified.     

Effects of lipase on poly(lactic acid) fibers

Two types of lipases, L3126 and Lipex 100L, were used to modify the surface of poly(lactic acid) (PLA) fiber by measuring weight loss percentage and wettability of the fiber in this work. The influence factors were discussed and optimized based on single-factor experiments. The optimal conditions for the modification of poly(lactic acid) fiber with lipases were determined as follows: incubation with lipase L3126 of 0.5 g/l at 45 °C and pH 8.5 for 8 hours and incubation with lipase of 10 ml/l at 40 °C and pH 7.5 for 10 hours. Lipase L3126 showed higher biodegradation ability to poly(lactic acid) fiber than lipase Lipex 100L. The scanning electron microscopy confirmed that both of the two lipases could lead to the formation of etching characters on treated poly(lactic acid) fibers in comparison with the blank samples. Furthermore, the wettability of the fibers treated with the lipases was evidently improved, especially Lipase L3126.     

Structure and performance of fibers prepared from liquefied wood in phenol

The fibers from liquefied wood in phenol (WPFs) were spun by adding hexamethylenetetramine as synthetics and cured by soaking in solution containing hydrochloric acid and formaldehyde as main components. The chemical structure of WPFs remarkably changed from that of liquefied wood was identified by FT-IR spectrometer. WPFs with the average diameter of 27∼42 μm, tensile strength of 230∼356 MPa, and modulus of 15∼31 GPa were obtained using spinning speed of 0.72 μm min⁻¹, hydrochloric acid concentration of 18.5 %, heating rate of 10 °C h⁻¹, and curing time of 4 h. These WPFs showed a high thermal stability and a complex thermal decomposition process by TG(thermogravimetric) analysis. It was also found that the two obvious weight loss temperatures of WPFs were 510°C and 748°C.     

Mechanical properties of flax-g-poly(methyl acrylate) reinforced phenolic composites

In order to develop composites with better mechanical properties and environmental performance, it becomes necessary to increase the hydrophobicity of the natural fibers and to improve the interface between matrix and natural fibers. Graft copolymerization of natural fibers is one of the best methods to attain these improvements. Only few workers have reported the use of graft copolymers as reinforcing material in the preparation of composites. So in the present paper, we report the preparation of graft copolymers of flax fibers with methyl acrylate (MA) using Fenton’s reagent (FAS-H₂O₂) as redox system. Synthesized flax-g-poly(MA) was characterized with FTIR, TGA/DTA, scanning electron microscopy (SEM), and X-ray diffraction (XRD) techniques. Composites were prepared using flax-g-poly(MA) as a reinforcement and phenolformaldehyde (PF) as the binding material. Mechanical properties of phenol-formaldehyde composites were compared and it has been found that composites reinforced with flax-g-poly(MA) showed improvement in mechanical properties. Composites reinforced with flax-g-poly(MA) showed better tensile strength (235 N) and compressive strength (814 N) in comparison to composites reinforced with original flax fiber which showed lesser tensile strength (162 N) and compressive strength (372 N). Composites reinforced with flax-g-poly(MA) shows the improved MOR, MOE, and SP.     

Thermal degradation behaviors and fire retardant properties of poly(1,3,4-oxadiazole)s (POD) and poly(m-phenylene isophthalamide) (PMIA) fibers

Thermal degradation behaviors and fire retardant properties of poly(1,3,4-oxadiazole)s (POD) and poly(m-phenylene isophthalamide) (PMIA) fibers were investigated. The thermal gravimetric analysis (TGA) demonstrated that POD exhibited higher onset thermal degradation temperature (T_onset) than PMIA, exceeding nearly 80 °C. The thermal degradation kinetics, evaluated by the modified Coats-Redfern method, displayed that the apparent activation energy (E_a) of POD and PMIA fibers was similar when the conversion rate (α) ranges from 0.2 to 0.5, while with the α from 0.6 to 0.8, the E_a of POD was significantly lower than that of PMIA. The fire retardant performance of POD and PMIA fibers were evaluated by cone calorimeter under heat fluxes of 35, 50 and 75 kW/m², during which the temperature of the fibers were monitored by a thermocouple. Surprisingly, POD fibers showed inferior fire retardant performance in comparison with PMIA, with lower time to ignition (TTI) and higher peak heat release rate (PHRR). The origin of the different fire retardant properties of both fibers was revealed by analyzing the residual chars and gaseous products during thermal pyrolysis. The morphology confirmed that stable and compact chars can be formed in PMIA. In addition, the Fourier Transform Infrared Spectroscopy (FTIR) characterization of the residual char revealed that POD can form carbonaceous chars at the heat flux of 50 kW/m², while the heat flux of PMIA was 75 kW/m². The pyrolysis products characterized by pyrolysis-gas chromatography-mass spectrometry (Py-GC-MS) indicated that POD can be pyrolyzed completely at 600 °C, while the temperature of PMIA was 700 °C.     

Preparation and characterization of nanoscaled poly(vinyl alcohol) fibers via electrospinning

Nanoscaled PVA fibers were prepared by electrospinning. This paper described the electrospinning process, the processing conditions, fiber morphology, and some potential applications of the PVA nano-fibers. PVA fibers with various diameters (50–250 nm) were obtained by changing solution concentration, voltage and tip to collector distance (TCD). The major factor was the concentration of PVA solution which affected the fiber diameter evidently. Increasing the concentration, the fiber diameter was increased, and the amount of beads was reduced even to 0%. The fibers were found be efficiently crosslinked by glyoxal during the curing process. Phosphoric acid was used as a catalyst activator to reduce strength losses during crosslinking. Scanning electron micrograph (SEM) and differential scanning calorimetric (DSC) techniques were employed to characterize the morphology and crosslinking of PVA fibers. It was found that the primary factor which affected the crosslinking density was the content of chemical crosslinking agent.     

Fabrication and properties of dope-dyed Poly(m-phenylene isophthalamide) fibers via wet spinning

Poly(m-phenylene isophthalamide) (PMIA) fibers play an irreplaceable role in the area of high-temperature resistance. It is usually difficult to dye PMIA fibers due to their rigid molecular structure and high crystallinity. In this study, the dope-dyed PMIA fibers with different amounts of pigment were fabricated by wet spinning. The properties of the pigment were analyzed, including size distribution and dispersive properties. The results showed that the pigment was easy to disperse in the fibers when the average diameter of the pigment was smaller than 500 nm. The color fastness of the colored PMIA fibers was tested, and their thermal properties and mechanical properties were also analyzed. The results of thermal gravity analysis (TGA) indicated that the colored PMIA fibers maintained good thermal performance. Compared to uncolored PMIA fibers, the colored PMIA fibers became lighter after exposing to simulated sunlight for 50 h. The breaking tenacity of fibers exceeded 2.0 cN/dtex, and the retentivity was above 80 % after being exposed to simulated sunlight for 50 h. These suggested the good mechanical performance of colored PMIA fibers. Dope-dyed PMIA fibers with good mechanical properties and thermal performance were successfully developed.     

Development and characterization of alginate-chitosan-hyaluronic acid (ACH) composite fibers for medical applications

Natural materials and plants have a long history of medical applications due to their broad range of favorable biological functions including biocompatibility, anti-bacterial, anti-oxidant and anti-inflammatory properties. Main objective of this study was to develop alginate-chitosan-hyaluronic acid (ACH) composite fibers with controlled drug release, and liquid retention properties for better moist wound healing. The dope comprising sodium alginate was extruded into calcium chloride (CaC1₂) coagulation bath. The developed calcium alginate fibers were then passed through a bath containing hydrolyzed chitosan and dip coated with hyaluronic acid for 24 hours. The resulting ACH composite fibers were then rinsed with deionized water and dried using acetone. These fibers were tested for tensile properties, % swelling, liquid absorption (g/g) and controlled drug release. The results concluded that ACH composite fibers can be produced by wet spinning and have adequate tensile properties, high % swelling, liquid absorption (g/g) and controlled release of hyaluronic acid for improved wound healing.     

Dyeing of cotton and silk yarn with the extracted dye from the fruit hulls of mangosteen,<Emphasis Type="Italic">Garcinia mangostana</Emphasis> linn

The extracted dye from the dried fruit hulls of mangosteen was used as a natural dye for the dyeing of cotton and silk yarn. The optimal conditions for dye extraction were to extract the dried fruit hulls of mangosteen at 80°C for 1 hour with a 15 % w/v citric acid solution in a 1:4 ratio of mangosteen powder to solvent. Cotton dyeing with the extracted dye from the dried fruit hulls of mangosteen was carried out at 60°C for 60 minutes with a material to liquor ratio of 1:25. The effect on dyeing of mordant type with different mordanting methods was studied. The results showed that the dyeing of cotton using the post-mordanting method with ferrous sulfate and calcium hydroxide not only provided better depth of shade but also provided better wash fastness and light fastness than with other mordants (alum; zinc tetrafluoroborate) or without a mordant. Good fastness properties were also obtained using a post-mordanted silk with calcium hydroxide.