Depositon of ZnO on polyacrylonitrile fiber by thermal solvent coating

In this study, the surface functionalization of polyacrylonitrile (PAN) fibers was achieved by depositing ZnO nanoparticles using thermal solvent coating. surface morphology, crystalline structure, surface chemistry, thermal stability and washing stability of the ZnO coated PAN fibers were investigated by scanning electron microscope (SEM), X-ray diffractometer (XRD), Fourier transform Infra red spectroscopy (FT-IR), Thermo-gravimetric analyses (TGA) and washing stability test, respectively. In addition, the weight changes after coating and washing were studied at different coating and washing conditions. The SEM images revealed that the ZnO was well coated on the surface of the PAN fibers and the coating was obviously affected by the experimental temperature. The FT-IR spectra indicated the chemical features of the deposited ZnO nanostructures. The XRD patterns showed that there was a typical crystalline structure of ZnO nanogains formed on the PAN fibers after coating. The TGA results revealed that the thermal stability of the PAN fibers was improved by the ZnO coating. The experimental results of washing stability revealed the effect of temperature on the washing stability. Weight measurements indicated that the amount of ZnO deposited on PAN fibers increased with the increasing of coating temperature from 60 to 70 °C. Weight measurements also revealed that the weight of the ZnO coating on fibers decreased with the increase in washing temperature and washing time.     

Manufacturing and analyses of wet-laid nonwoven consisting of carboxymethyl cellulose fibers

Carboxymethyl cellulose (CMC) is a cellulose derivative having water-soluble property, biodegradability, and biocompatibility. It has been used in various medical applications as forms of gel, film, membrane, or powder. In this study, composite CMC nonwovens were produced, by a wet-laid nonwoven process, to improve the wet strength of carboxymethyl cellulose nonwovens. Followed by preparing the CMC fibers from cotton fiber, the composite CMC nonwovens composed of CMC fibers and PE/PP bicomponent fibers were manufactured by using 85/15 % v/v of ethanol/water solution as a dispersion medium. Structural analyses of CMC fibers, such as XRD, TGA, FT-IR, and degree of substitution indicated that CMC fibers were successfully produced. The wet strength of CMC nonwoven was dramatically increased by blending with the PE/PP fibers without sacrificing the key properties for wound dressing materials such as liquid absorption, gel blocking and liquid retention. It is expected that the composite CMC nonwovens will be a good candidate for wound dressing materials for mild exudate condition.     

Effect of chemically modified date palm leaf fiber on mechanical,thermal and rheological properties of polyvinylpyrrolidone

Polyvinylpyrrolidone/date palm leaf fiber (PVP/DPL) biocomposites were prepared by melt mixing fabrication technique with different weight percentage of fibers. DPL fibers were chemically modified by acrylic acid in order to have better dispersion and compatibility with PVP matrix. The interaction of DPL fibers with PVP matrix was studied by Fourier transforms infrared spectroscopy (FTIR). Field emission scanning electron microscope (FESEM) was used for the study the morphology of chemically modified DPL fibers and PVP/DPL biocomposites. Mechanical properties were improved with fiber loading due to strong interfacial adhesion between PVP and DPL fibers. The storage modulus, loss modulus and tan delta values of PVA/DPL biocomposites were measured by DMTA. The rheological properties were investigated to study the shearing storage and loss modulii along with complex viscosity of biocomposites. The thermal and conducting properties of biocomposites were measured and compared with that of virgin PVP.     

Highly stable coated polyvinylpyrrolidone nanofibers prepared using modified coaxial electrospinning

Hydrophobic polyvinylpyrrolidone (PVP) nanofibers, which is intensely hygroscopic, has been successfully prepared to improve their moisture resistance using a modified coaxial electrospinning process. A stearic acid (SA) solution was exploited as the sheath fluid to coat the fibers. Scanning electron microscopy demonstrated that the SA-coated PVP nanofibers became increasingly small with a rise in the sheath-to-core flow rate ratio; continuing to increase the sheath flow rate beyond a cut-off point resulted in nanofibres with very complicated morphologies. Transmission electron microscope images showed that SA formed a thin layer on the PVP nanofibers, with SA nanoparticles present on the fiber surfaces when a sheath-to-core flow rate ratio of 0.2:0.8 was used. Attenuated total reflectance-Fourier transform infrared spectroscopy verified the coating of SA onto the PVP nanofibers, and also the formation of hydrogen bonds between the SA and PVP molecules. The SA-coated PVP nanofibers were found to have much enhanced moisture resistance over pure PVP fibers. Modified coaxial electrospinning hence comprises a novel and powerful strategy for nanocoating and surface modification of polymer nanofibers.     

Electrospun poly(tetrafluoroethylene) nanofiber membranes from PTFE-PVA-BA-H<Subscript>2</Subscript>O gel-spinning solutions

As a kind of high-performance fibers, PTFE fiber has been widely used in many fields because of its unique characteristics. In this study, the poly(tetrafloroethylene) (PTFE) nanofibers manufactured by electrospinning method was reported. The gel-spinning solution of poly(tetrafluoroethylene)/poly(vinyl alcohol)/boric acid (PTFE/PVA/BA), which was prepared by the gel process of the mixture of PTFE, PVA, BA and redistilled water, was electrospun to form PTFE/PVA/BA composite nanofibers. After calcinating, the PTFE nanofibers with diameters of 200 nm to 1000 nm were obtained. The fibers before and after calcinating were characterized by scanning electron microscopy (SEM), thermogravimetric analysis (TGA), X-ray diffraction (XRD), FT-IR spectrum analysis and X-ray photoelectron spectroscopy (XPS), respectively, and the mechanical and hydrophobic properties of the fibers were also investigated. The results showed that the PTFE nanofiber membranes could be electrospun effectively used the gel-spinning solution of PTFE/PVA/BA, and may realize the applications in the fields of high-temperature filtration, catalyst supports, battery separator and so on.     

Effects of surface treatment of ramie fibers in a ramie/poly(lactic acid) composite

The chemical and morphological properties of ramie fibers treated by chemical surface modification were examined with Fourier transform infrared (FT-IR) spectroscopy. The mechanical and thermal decomposition properties were evaluated with respect to tensile strength, tensile modulus and thermogravimetric analysis (TGA). Surface morphological changes were investigated with scanning electron microscopy (SEM). Finally, the capabilities of composites reinforced with various chemically treated fibers were analyzed by investigating tensile and impact strengths. Additionally, the thermal mechanical properties of the composites were investigated with thermal mechanical analysis (TMA). Based on the results of these analyses, we concluded that pectin, lignin and hemicellulose were removed and thermal stability was increased with chemical treatments. The composites reinforced with ramie fiber showed better properties compared with pure PLA matrix with respect to tensile and impact strengths. The peroxide-treated fiber composite had the smallest thermal expansion.     

Effect of surface treatment of jute fibers on the interfacial adhesion in poly(lactic acid)/jute fiber biocomposites

Jute fibers have immense potential to be used as natural fillers in polymeric matrices to prepare biocomposites. In the present study jute fibers were surface treated using two methods: i) alkali (NaOH) and ii) alkali followed by silane (NaOH+Silane) separately. Effects of surface treatments on jute fibers surface were characterized using fourier transform infrared spectroscopy (FT-IR) and scanning electron microscopy (SEM) analyses. Further, the effects of surface treatments on jute fibers properties such as crystallinity index, thermal stability, and tensile properties were analyzed by X-ray diffraction method (XRD), thermo gravimetric analysis (TGA), and single fiber tensile test respectively. The effects of surface treatment of jute fibers on interphase adhesion between of poly(lactic acid) (PLA) and jute fibers were analyzed by performing single fiber pull-out test and was examined in terms of interfacial shear strength (IFSS) and critical fiber length.     

Processing and characterization of nickel-plated PBO fiber with improved interfacial properties

A new application of conventional electroless nickel plating to improve the interfacial properties of PBO fibers was reported. The relationship between surface morphology and interfacial properties of nickel-plated PBO fiber was explored. The continuous nickel coating consisted of nickel and phosphorus elements determined by Energy dispersive spectrometer (EDS) and transmission electron microscope (TEM), exhibiting high adhesive durability. The influence of bath temperature and plating time on the crystal structure, microstructure and mechanical properties of nickel-plated PBO fibers was systematically investigated. X-ray diffractometer (XRD) results revealed that the crystal structure among nickel-plated PBO fibers did not show differences. Scanning electron microscope (SEM) and Atomic force microscope (AFM) images showed that the process parameters had a great influence on surface morphology and roughness of nickel-plated PBO fibers, which could directly affect the interfacial properties of nickel-plated PBO fibers. Single fiber pull-out testing results indicated that the interfacial shear strength (IFSS) of PBO fibers after electroless nickel plating had a significant improvement, which reached maximum at 85 °C for 20 min. Single fiber tensile strength of nickel-plated PBO fibers was slightly lower than that of untreated one. Thermo gravimetric analysis (TGA) indicated that nickel-plated PBO fiber had excellent thermal stability.     

Sulfur-modified chitosan hydrogel as an adsorbent for removal of Hg(II) from effluents

Sulfur-modified chitosan hydrogel (SMCH) was successfully synthesized by grafting dimethyl 3,3′-dithiodipropionate onto chitosan and then crosslinking with N,N′-methylene diacrylamide (MBA). The structure and properties of chitosan and sulfur-modified chitosan (SMC) were characterized and analyzed by Fourier transform infrared spectroscopy (FT-IR), Nuclear magnetic resonance (¹H NMR), X-ray diffraction (XRD) and Thermogravimetric analysis (TGA). Meanwhile, chitosan hydrogel and SMCH were characterized by Scanning electron microscope (SEM). In addition, static adsorption Hg(II) ions properties of chitosan hydrogel and SMCH were also investigated. The FT-IR and ¹H NMR manifested that SMC was synthesized successfully. The XRD and TGA showed that the crystallinity and thermal stability of SMC decreased. SEM showed that the SMCH had much more pores and bigger specific surface area than chitosan hydrogel. The result of adsorption experiment indicated that the SMCH showed noticeable improvements in the adsorption capacity of Hg(II), and had the highest adsorption capacity (187.5 mg/g) at pH 5.0. The equilibrium was achieved at 40 min. And the maximum adsorption capacities were 186.9 mg/g of SMCH.     

Effects of carbon nanotubes on morphological structure, thermal and flammability properties of electrospun composite fibers consisting of lauric acid and polyamide 6 as thermal energy storage materials

The ultrafine composite fibers consisting of lauric acid (LA) and polyamide 6 (PA6) as form-stable phase change materials (PCMs), were prepared successfully by electrospinning. The effect of carbon nanotubes (CNTs) on the structural morphology, phase change behaviors, thermal stability, flammability and thermal conductivity properties of electrospun LA/PA6 composite fibers was investigated by field-emission scanning electron microscopy (FE-SEM), differential scanning calorimetry (DSC), thermogravimetric analyses (TGA), microscale combustion calorimeter (MCC) and melting/freezing times measurements, respectively. SEM observations indicated that the LA/PA6 and LA/PA6/CNTs composite fibers possessed flat and ribbon-shaped morphologies, but the neat PA6 fibers had cylindrical shape with smooth surface; and the average fiber diameters for LA/PA6 composite fibers decreased generally with the addition of CNTs. DSC measurements indicated that the heat enthalpies of the composite fibers were lower that that of neat LA powders, while the amounts of CNTs had no appreciable effect on the phase change temperatures and heat enthalpies of the composite fibers. TGA results showed that the addition of CNTs increased the onset thermal degradation temperature, maximum weight loss temperature and charred residue at 700 °C of the composite fibers, attributed to the improved thermal stability properties. It could be found from MCC tests that there were two-step combustion processes for composite fibers, and corresponded respectively to combustion of LA and polymer chains (PA6) in composite fibers. The addition of CNTs reduced the peak of heat release rate (PHRR) of electrospun composite fibers, contributing to the decreased flammability properties. The improved thermal conductivity performances of LA/PA6/CNTs composite fibers was also confirmed by comparing the melting/freezing times of LA/PA6 composite fibers with that of neat LA powders. The results from the SEM observation showed that the composite fibers had no appreciable variations in shape and diameter after heating/cooling processes.     

Enzyme-modified casein fibers and their potential application in drug delivery

Enzymatic crosslinking of casein fibers was done using Transglutaminase (TGase) to improve the mechanical properties, particularly the stability in aqueous conditions and make them suitable for controlled drug release application. Crosslinking casein with 5 U/g of TGase in the spinning dope for 60 min at 25 °C increased the tenacity and tensile strain of the fibers from 0.40 g/den and 4.2 % to 0.70 g/den and 23.1 %, respectively. The stability of the fibers in water at different pH levels was considerably improved after the enzymatic crosslinking. The SDS-PAGE electrophoresis confirmed that higher molecular weight proteins were formed in TGase-crosslinked fibers. Thermogravimetric analysis (TGA) showed that TGase treated fibers also had a higher thermal degradation temperature than the non-crosslinked fibers. Crosslinked fibers exhibited delayed and lower rate of drug release from the fibers suggesting their suitability for controlled drug release.     

The effect of zinc ion content on flame retardance and thermal degradation of alginate fibers

The study employs limiting oxygen index (LOI) measurements, cone calorimetry (CONE) and thermogravimetric analysis (TGA) to examine the catalytic effect of zinc ion content on the flame retardance and thermal degradation of alginate fibers. LOI results show that all zinc alginate fibers are intrinsically flame retardant, with LOI values of over 27.0, as compared with about 24.5 for alginic acid fiber. The heat release rate (HRR) and total heat release values of zinc alginate fibers (obtained from CONE) are significantly less than those of alginic acid fiber, and decrease with increasing zinc ion content. TGA indicates that char formation increases and maximum thermal weight-loss rate is reduced when zinc content in the fibers is increased. The residues of zinc alginate fibers keep their shapes better than those of the alginic acid fiber. Further discussion of the combustion process and flame retardant mechanism is presented.     

蔗糖脂肪酸三酯在菜籽油脱磷工艺中的应用及蔗糖酯磷脂复合物的制备

本文以蔗糖脂肪酸三酯（sucrose fatty acid triester，STE）和磷脂酰胆碱（phosphatidylcholine，PC）为原料制备蔗糖酯磷脂复合物，并通过傅里叶红外光谱分析（Fourier infrared spectrum，FT-IR）、热重分析（thermogravimetric analysis，TGA）和差示扫描量热分析（differential scanning calorimetry，DSC）对制备的蔗糖酯磷脂复合物进行表征分析；以STE为吸附脱磷剂，考察STE在菜籽油脱磷工艺中的应用。研究结果表明，STE与PC在无水乙醇体系中形成了新型的STE-PC复合物，与STE和PC相比，STE-PC复合物具有更低的相变熔融温度；另外，STE对菜籽油中的磷脂有一定的吸附脱除作用，在脱磷温度为55oC、STE添加量为3.5%、脱磷时间为30min条件下，脱磷率可达37.2%。     

Effect of peroxide and softness modification on properties of ramie fiber

Ramie fiber is one of the natural cellulose fibers that have undergone rapid development due to its good performance. This study confirmed that hydrogen peroxide and isopropyl alcohol can be used as very efficient agents for simultaneous removal of non-cellulosic substances and improvement of ramie fiber properties. The factors influencing the properties of modified fiber with combined chemicals were investigated. Optimum treatment conditions were achieved at 85 °C, 60 min, pH 11.0, hydrogen peroxide concentration 7 %, and isopropyl alcohol concentration 4 %. SEM, XRD, and FT-IR were used to elucidate the effects of preparation and modification. Results showed that fiber preparation and chemical modification process in the same bath solution could successfully remove most of the gummy materials. The treated fibers demonstrated improved softness, elongation, and fineness properties as compared to the alkali or peroxide method.     

An effective and simple process for obtaining high strength silkworm (Bombyx mori) silk fiber

This article describes a new process for strengthening natural silk fibers. This process is simple yet effective for mass production of high strength silk fibers, enabled by drawing at a lower temperature and immediately heat setting at a higher temperature. The processing conditions were investigated and optimized to improve the strength. Silk fibers drawn to the maximum ratio at room temperature and then heat set at 200 °C show best tensile properties. Some salient features of the resulting fibers are tensile strength at break reaching 533±10.2 MPa and Young’s modulus attaining 12.9±0.57 GPa. These values are significantly higher than those of natural silk fibers (tensile strength increased by 44 % and Young’s modulus by 135 %). Wide-angle X-ray diffraction and FTIR confirm the transformation of silk I to silk II crystalline structure for the fiber obtained from this process. DSC and TGA data also provide support for the structural change of the silk fiber.     

Effect of temperature and durations of heating on coir fibers

Biocomposites derived from polymeric resin and lignocellulosic fibers may be processed at temperatures ranging from 100 °C to 230 °C for durations of up to 30 min. These processing parameters normally lead to the degradation of the fiber's mechanical properties such as Young's modulus (E), ultimate tensile strength (UTS) and percentage elongation at break (%EB). In this study, the effect of processing temperature and duration of heating on the mechanical properties of coir fibers were examined by heating the fibers in an oven at 150 °C and 200 °C for 10, 20 and 30 min to simulate processing conditions. Degradation of mechanical properties was evaluated based on the tensile properties. It was observed that the UTS and %EB of heat treated fibers decreased by 1.17-44.00% and 15.28-81.93%, respectively, compared to untreated fibers. However, the stiffness or E of the fibers increased by 6.3-25.0%. Infra red spectroscopy (FTIR), thermogravimetric analysis (TGA) and scanning electron microscopy (SEM) were used to elucidate further the influence of chemical, thermal and microstructural degradation on the resulting tensile properties of the fibers. The main chemical changes observed at 2922, 2851, 1733, 1651, 1460, 1421 and1370 cm⁻¹ absorption bands were attributed to oxidation, dehydration and depolymerization as well as volatization of the fiber components. These phenomena were also attributed to in the TGA, and in addition the TGA showed increased thermal stability of the heat treated coir fibers with reference to the untreated counterparts which was most probably due to increased recrystallization and cross linking. The microstructural features including microcracks, micropores, collapsed microfibrils and sort of cooled molten liquid observed on the surface of heat treated coir fibers from the scanning electron microscope (SEM) could not directly be linked to the effect of temperature and durations of heating although such features may have largely account for the lower tensile properties of heat treated coir fibers with reference to untreated ones.     

Water soluble carboxymethylcellulose fibers derived from alkalization-etherification of viscose fibers

Carboxymethylcellulose (CMC) fibers have been successfully prepared from viscose fibers through the process of alkalization-etherification. Parameters including reaction temperature, mass ratio of NaOH to the viscose fibers, and mass ratio of the viscose fibers to ethanol are studied. The degree of substitution (DS) and the inherent viscosity of the CMC fibers are determined. The CMC fibers are characterized by using Fourier transform infrared spectroscopy (FT-IR), ¹H-nuclear magnetic resonance spectroscopy (¹H-NMR), scanning electron microscopy (SEM), and the X-ray diffraction (XRD). The analysis demonstrates that under the experimental conditions where the reaction temperature is 40 °C, mass ratio of NaOH to the viscose fibers is 2.0, and mass ratio of the viscose fibers to ethanol is 1:15, the obtained CMC fibers possess an appropriate DS, better water-solubility, and lower degree of etching, thus they can be used as absorbable hemostatic fibers.     

The role of Na-montmorillonite on thermal characteristics and morphology of electrospun PAN nanofibers

Polymer organic-inorganic hybrid nanofibers constitute a new class of materials in which the polymeric nanofibers are reinforced by uniformly dispersed inorganic particles having at least one dimension in nanometer-scale. In the present study, polyacrylonitrile (PAN) and PAN/Na-montmorillonite (PAN/Na-MMT) nanofibers were conducted via electrospinning process. Electrospun PAN and PAN/Na-MMT fibers with the respective mean fiber diameter of about 220 and 160 nm were prepared. The influence of the clay-montmorillonite on the morphology and diameter of nanofibers was investigated by scanning electron microscope (SEM) and transmission electron microscope (TEM) techniques. The microscopic techniques propose that the PAN/Na-MMT composite nanofibers show lower mean fiber diameter than the neat PAN nanofibers. Besides, the difference in nanoclay-content has a slight effect on the distribution of fibers diameter. Thermogravimetric analysis (TGA) results suggest that introduction of clay-nanomaterials improves the thermal characteristics of fibers.     

An investigation on the comparison of wet spinning and electrospinning: Experimentation and simulation

Polysulfonamide (PSA) has been widely used in many fields because of its excellent thermodynamic properties. In this study, PSA fibers were prepared separately via two different spinning ways, including conventional wet spinning and electrospinning. Fluid motion of wet spinning and electrostatic field of electrospinning were modeled using finite element analysis to investigate the spinning process. The properties of fabricated PSA fibers were characterized systematically by scanning electron microscope (SEM), fourier transform infrared spectrometer (FTIR), X-ray diffraction (XRD), thermal gravity analysis (TGA) and electronic strength tester. Based on the simulation and theoretical analysis of spinning process, it was found that the extruding force of the wet spinning is larger than that of the electrospinning. The larger extruding force makes the alignment of macromolecules inside fiber relatively uniform, and a higher proportion of crystallization happens. Accordingly, the mechanical properties and thermal stability of PSA fibers could be improved due to a higher proportion of crystallization. The experimental results of mechanical strength and TG test are coincided with the simulation results. PSA fiber prepared by wet spinning has better thermal stability and mechanical properties than that fabricated by electrospinning.     

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.