Synthesis,structure and thermal protective behavior of silica aerogel/PET nonwoven fiber composite

In recent years, flexible, mechanically strong and environmental friendly thermal insulation materials have attracted considerable attention. In this work, silica aerogel/polyethylene terephthalate (PET) nonwoven fiber composite with desirable characteristics was prepared via a two-step sol-gel process followed by an ambient drying method through immersing the PET nonwoven fiber into silica sol. The silica aerogel particles were characterized by FTIR, FE-SEM, TGA and nitrogen adsorption analysis. The morphology and hydrophobic properties of neat PET nonwoven fiber and its silica aerogel composite were also investigated. For studying thermal protective properties, the thermal diffusivity was calculated from temperature distribution curves. The mean pore size of 11 nm, the surface area of 606 m²/g and the total pore volume of 1.77 cm³/g for the silica aerogel particles in the composite are obtained from nitrogen adsorption analysis, indicating the aerogel can maintain its high porosity in the nonwoven composite structure. Silica aerogel particles were efficiently covered the surface of the PET fibers and completely filled the micron size pores of the nonwoven fiber leading to a stronger hydrophobicity and higher thermal insulation performance in the aerogel composite samples compared to the neat PET nonwoven. In this regard, an almost 64 % decrease in the thermal diffusivity was achieved with 66 wt% silica aerogel.     

Effect of surface treatment on the structure and properties of para-aramid fibers by phosphoric acid

The surface of para-aramid fiber was modified by phosphoric acid solutions (H3PO4) based on an orthogonal experimental design and analysis method. Statistical results indicate that treatment temperature is the most significant variable in the modification processing, while treatment time was the least important factor. The structure and morphology of the modified fiber were characterized by Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), X-ray diffraction instrument (XRD), and scanning electron microscope (SEM). The results showed that some polar groups were introduced into the molecular structure of aramid fibers and the physical structure of the treated fibers was not etched obviously. The interfacial properties of aramid fiber/epoxy composites were investigated by the single fiber pull-out test (SFP), and the mechanical properties of aramid fibers were investigated by the tensile strength test. The results showed that the interfacial shear strength (IFSS) of aramid/epoxy composites was remarkably improved and the breaking strength of aramid fibers was not affected appreciably after surface modification.     

High Velocity Impact Response of Basalt Fibers/Epoxy Composites Containing Graphene Nanoplatelets

The effects of adding surface modified graphene nanoplatelets (GNPs) in various weight percentages (0, 0.1, 0.2, 0.3, 0.4, 0.5 with respect to matrix) on the high velocity impact response of basalt fibers/epoxy composites were evaluated. High speed mechanical stirrer and ultrasonic waves were used for the dispersion of GNPs in the epoxy matrix, and hand layup method was utilized for the fabrication of the composite samples. High velocity impact testing was performed using a conical projectile. The results demonstrated that the maximum improvement in the impact limit velocity and energy absorption occurred in the 0.3 wt.% GNPs nanocomposite, i.e., 11 and 23 %, respectively. Also, the electron microscopy studies revealed that the addition of GNPs contributed in improving the impact properties by influencing the matrix and thus enhancing the interfacial characteristics between the basalt fibers and the matrix.     

Ultra-porous flexible PET/Aerogel blanket for sound absorption and thermal insulation

Ultra porous and flexible PET/Aerogel blankets were prepared at ambient pressure, and their acoustic and thermal insulation properties were characterized. Two methods were selected for the preparation of PET/Aerogel blanket. Method I was a direct gelation of silica on PET. PET non-woven fabric was dipped and swelled in TEOS/ethanol mixture, and pH of reaction media was controlled to 2.5 using HCl to promote hydrolysis. After acid hydrolysis, pH was controlled to 7,8,9, and 10 with NH₄OH for the condensation. Method II was by the dipping of PET non-woven fabric in the dispersion of Silica hydrogel. The gelation process was same with Method I. However, PET fabric was not dipped in reaction media. After the hydrogel was dispersed and aged in EtOH for 24 hrs, then, PET non-woven fabric was dipped in the dispersion of hydrogel/EtOH for 24 hrs. The surface modification was carried out in TMCS/n-hexane solution, then the blanket was washed with nhexane and dried at room temperature to prevent the shrinkage. The silica areogels synthesized in optimum conditions exhibit porous network structure. Silica aerogel of highly homogeneous and smallest spherical particle clusters with pores was prepared by gelation process at pH 7. When direct gelation of silica was performed in PET nonwoven matrix (Method I), silica aerogel clusters were formed efficiently surrounding PET fibers forming network structure. The existence of a great amount of silica aerogel of more homogeneous and smaller size in the cell wall material has positive effect on the sound absorption and thermal insulation.     

Modification of enzyme pretreated cotton fabric using acrylonitrile, acrylonitrile/solvent mixture and its characterization

The presented research deals with modifying the chemical structure of the bioscoured cotton fabric by acrylonitrile, acrylonitrile/acetone, and acrylonitrile/ethanol mixture. The modified cellulose was tested for weight gain, shrinkage, and wicking height and characterized by X-ray diffraction (XRD), thermal analysis (TG/DTA), elemental analysis, Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and atomic force microscopy (AFM). The weight gain and shrinkage % show increased value for modified fabrics. The wicking height increases with addition of solvent. The crystallinity and thermal studies show a significant change. FTIR analysis confirms the modification by the occurrence of -C??N stretching and -CONH₂ stretching. The SEM morphology of modified fabric shows uniform swelling of fibers with better smoothness. The AFM topography reveals that the addition of solvent affects the particle size. Clear surface morphology of modified fabric reveals that this processing method can be used for preparation of medical textiles with more swelling.     

Effect of Basalt Fiber on the Strength Properties of Polymer Reinforced Sand

This paper displays an experimental study of the effect of basalt fiber on the strength properties of polymer reinforced sand. Laboratory trials of unconfined compression test (UCS), direct shear test, and tensile test were conducted on the specimens treated with polymer and basalt fiber, and several factors including polymer content, fiber content and dry density of sand that will influence the strength behaviors are investigated in detail. Based on test results and scanning electron microscope (SEM) images, the reinforcement mechanism was analyzed. The results showed that the polymer content, basalt fiber content and dry density of sand had greatly improved the strength behaviors of reinforced specimens. The increase in polymer and fiber content had an active effect on strength characteristics, while the angle of internal decreased slightly. The strength properties were enhanced with the increase in dry density, and the effect of dry density on tensile strength is affected by fiber content. The presence of randomly distributed fibers has formed a spatial fiber-sand net in sand, and the additive of polymer solution formed membrane to enwrap sand particles and connect sand and fibers, thereby formed a stable structure in sand. These structures have increased the bonding and interlocking forces between sand and fibers, and decreased the void ratio of reinforced specimens.     

Thermal Insulation Performance of Cotton and PET-based Hybrid Fabrics Impregnated with Silica Aerogel via a Facile Dip-dry Process

We report the morphological features and thermal insulation properties of a series of cotton- and PET-based hybrid fabrics impregnated with silica aerogel. For the purpose, commercially available cotton and PET knitted fabrics were dipped into aqueous dispersions including different silica aerogel contents, dried, and stacked to 1, 3, and 5 layers. The SEM images revealed that the silica aerogel particles were well incorporated into cotton or PET knitted fabrics. The thermal insulating performance of the hybrid fabrics as functions of the silica aerogel content and the number of layers of stacked fabrics were characterized by monitoring the surface temperatures of the fabrics on a plate with a wide temperature range of ~50-80 oC using an infrared camera. The higher thermal insulation performance was attained for both cotton- and PET-based hybrid fabrics with higher silica aerogel contents. In addition, 3-layered hybrid fabrics exhibited noticeably improved thermal insulation performance, compared to 1- or 5-layered fabrics. The thermal insulation property of the cotton-based hybrid fabrics was dominantly influenced by silica aerogel than that of PET-based hybrid fabrics. The overall results demonstrated that the cotton- and PET-based hybrid fabrics with silica aerogel manufactured by a facile dip-dry process could be utilized as protective garments, heat-sensitive devices, pipes, automotive, aircrafts, and buildings for thermal insulation applications.     

Preparation and properties of alkaline functionalized carbon nanotubes reinforced polyurethane composites

Composites consisting of polyurethane (PU)/carbon nanotubes (CNTs) have been successfully prepared by solution mixing method. CNTs were modified through mechano-chemical reaction to increase the compatibility with PU via hydrogen bondings. SEM microphotographs proved that modified CNTs (M-CNTs) became shorter and FTIR spectra showed that hydroxyl groups had been introduced to the surface of M-CNTs. SEM images of PU/M-CNTs composites also proved that M-CNTs were effectively dispersed in PU matrix. Mechanical property tests showed that addition of M-CNTs could significantly improve the tensile properties of PU/M-CNTs composite (breaking strength enhancement ratio for composite with 5.0 wt% M-CNTs was 103.81 %). The thermal stability of composites with M-CNTs was also improved. The initial degradation temperature enhancement was 19.9 oC for the composite with 0.5 wt% M-CNTs. Electrical property tests showed that the electrical properties were improved by adding M-CNTs. The volume conductivities increased 3 and 5 orders of magnitude for the composites with 5.0 wt% and 10 wt% M-CNTs, respectively. The addition of M-CNTs had little effect on the elastic properties of the composites.     

Low-temperature pyrolysis on jute fibers as a thermochemical modification method

Low-temperature pyrolysis up to 200, 250, 300 °C was conducted in order to remove non-cellulosic compounds without damaging the structure of the cellulose in jute fibers. The chemical, morphological, and mechanical aspects of prepared low-temperature pyrolyzed jute fibers were investigated by Fourier transform infrared (FTIR) spectroscopy, the wettability test in water/dichloromethane system, moisture content measurement, X-ray diffraction (XRD) analysis, scanning electron microscope (SEM), and tensile test using universal testing machine (UTM). It was confirmed that hydrophilic compounds including absorbed water, low molecular weight compounds such as waxes, hemicellulose, and lignin were largely removed from the fibers. Increasing amounts of non-cellulosic compounds were removed as the maximum pyrolysis temperature was increased. The degree of hydrophilic nature of jute fibers were reduced by low-temperature pyrolysis and thus water absorptivity of pyrolyzed jute fibers was reduced as maximum pyrolysis temperature increased. Furthermore, XRD analysis and morphological studies by SEM indicated that the crystalline structure of native cellulose was rarely damaged after pyrolysis up to 300 °C. In case of mechanical properties, breaking tenacity and breaking strain of the fibers decreased with increasing maximum pyrolysis temperatures because flaws formed on the surface of pyrolyzed jute fibers acted as weak-links. In agreement with predictions made according to Weibull’s weakest-link theory, it was found that shortened pyrolyzed jute fibers could have higher breaking tenacities compared with raw jute fibers of the same length. In addition, the compatibility with hydrophobic matrix was investigated by the mechanical properties of polypropylene (PP) reinforced with jute fibers. Consequently, it was hypothesized that low-temperature pyrolysis could be used to process raw jute fibers for use as short fiber reinforcements in fiber-polymer systems or be a simple and effective pretreatment method for a wide range of further chemical treatments.     

Extraction of natural cellulosic fibers from cornhusk and its physico-chemical properties

A natural long staple ligno-cellulosic fibers have been extracted from the cornhusks using an alkali treatment. Physico-chemical properties such as chemical composition, length, fineness, crystallinity, surface properties, etc. measured by standard methods are reported in this paper. The physico-chemical and morphological properties of the extracted cornhusk fibers are discussed in detail and compared with other cellulosic like cotton and ligno-cellulosic fibers such as jute. Scanning electron microscopy was used to study the morphological and cross-sectional view and energy dispersive X-ray and FTIR were used for the identification and quantification of elements, groups present in the cornhusk and other cellulosic and lignocellulosic fibers. In addition, fibers are characterized by thermo-gravimetric analysis. Results showed that morphological and physico-chemical behavior is more or less similar to other multicellular ligno-cellulosic fibers like jute.     

Preparation,Characterization and Properties of High-salt-tolerance Sodium Alginate/Krill Protein Composite Fibers

Sodium alginate (SA) and krill protein (AKP) were blended to obtain composite solution, and functional SA/AKP composite fibers were prepared via wet spinning. To further improve the salt tolerance, SA/AKP composite fibers were modified with copper sulfate aqueous solution as secondary coagulation bath because of the strong adsorption to copper ions. The CSA/AKP composite fibers with high salt tolerance have been successfully prepared. The intermolecular interaction of SA/AKP composite system and the two-order structure of protein in the composite system were characterized by Fourier transform infrared spectroscopy (FT-IR). Besides, the crystallinity, morphology, mechanical properties, salt tolerance and water resistance and thermal stability of SA/AKP composites were investigated respectively. The results showed that the adsorption rate and the adsorption capacity of the composite solution to copper ion were significantly higher than those to calcium ion. Under the effect of secondary solidification by copper sulfate, the β-sheet chain of the composite fibers increased from 41.48 % to 49.21 %, the intramolecular hydrogen bond increased from 38.18 % to 44.26 %, the intermolecular hydrogen bond decreased from 59.84 % to 54.70 % and free hydroxyl slightly decreased. The water resistance of the modified composite fibers was improved by about 22 %; when the swelling time was 25 min, the salt resistance increased by about 150 %; the number of grooves on the surface of the composite fibers obviously increased, and the grooves on the surface of CSA/AKP composite fibers and the fiber section structure were much denser; Meanwhile, copper sulfate had some influence on the crystallization, thermal stability and mechanical properties of the composite fibers.     

Structural analysis of finer cotton yarns produced by conventional and modified ring spinning system

Yarn structure plays an important role in determining the properties of spun yarns. Recently, a modified spinning technique has been developed for producing a low torque and soft handle singles yarn by modifying the fiber arrangement in a yarn. Comparative studies revealed that the finer modified yarns possess significantly higher strength and lower hairiness over the conventional yarns of the same twist level, implying a different structure of finer modified yarn. Thus this paper aims to quantitatively study the structures of the finer conventional and modified cotton yarn (80 Ne) produced at the same twist level. Various measuring techniques, namely the Scanning Electron Microscope (SEM), cross section technique and tracer fiber technique, are adopted to analyze their structural characteristics, including fiber configuration, fiber spatial orientation angle, fiber packing density, yarn surface appearance, and fiber migration behavior. Results showed that finer modified yarns exhibit a smoother surface and much more compact structure with less hairiness. The fibers in the finer modified yarn have a complicated fiber path with relatively lower fiber radial position, larger migration frequency and magnitudes. In addition, it was noted that 73% of fibers in the finer conventional yarn follow concentric conical helix, which is contrary to those in the coarser conventional yarn. The analyses conducted in this paper provide deep insights into the mechanism of modified spinning technique and evidential explanations on the difference of properties between the finer conventional and modified yarns.     

硅溶胶浸注-热处理改性橡胶木物理性能初探

采用硅溶胶作为浸注改性液，分析橡胶木经过浸注及浸注-热处理改性后物理性能的变化。结果表明：浸注改性使橡胶木增重率提高约20%，气干密度提高15%，平衡含水率降低6%，径向及弦向气干湿胀率均降低20%左右；而橡胶木浸注-热处理材与热处理材相比，质量损失率降低15%，气干密度提升约15%，平衡含水率降低8%，径向及弦向气干湿胀率则分别降低约5%和20%。     

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

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

Synthesis and characterization of polyacrylate sizes modified by nano-microspheres prepared via miniemulsion polymerization

This paper firstly stated the fabrication of silica particles via Sol-Gel method and their modification by Silane coupling agent ??-MPS (3-Methacryloxypropyltrimethoxysilane). Pure PSt (Polystyrene) and silica/PSt microspheres were prepared via miniemulsion polymerization. We added these two microspheres to SX-5 size respectively to form the nanomodified sizes. These nano-particles were characterized by means of FTIR (Fourier Transmission Infrared Spectroscopy), DLS (Dynamic Light Scattering) and TEM (Transmission Electron Microscope). Then the properties of sizes (SX-5, nanomodified SX-5, PVA (Polyvinyl Alcohol) 1799), size films, sized yarns, and removability of sizes were characterized. Experimental results show that silica/PSt modified SX-5 had the best properties of sizes, and the best properties presented in size films and sized yarns. This result can be suggested that small size effect, high fluidity, high surface energy and tough surface morphology of silica/PSt microspheres, playing a role as cross-linker and reinforcement, will enhance the mechanical properties of SX-5 and increase the interfacial adhesion force between sizes and yarns.     

Surface modified ployacrylonitrile nanofibers and application for metal ions chelation

Ployacrylonitrile (PAN) nanofibers were formed by electrospinning. Amidoxime ployacrylonitrile (AOPAN) nanofibers were prepared by reaction with hydroxylamine hydrochloride, which were used as the matrix for metal ions chelation. FTIR spectra of the PAN nanofibers and AOPAN nanofibers were recorded for analysis of the surface chemical structures. The AOPAN conventional fibers were also prepared for comparison, and surface morphologies of the modified PAN conventional fibers and PAN nanofibers were observed by FESEM. Metal ions concentrations were calculated by AAS. The chelated isothermal process and kinetics parameters of the modified PAN nanofibers and PAN conventional fibers were studied in this work. Results indicated that the saturated coordinate capacity of AOPAN nanofibers to Cu²⁺, Cd²⁺ was 3.4482 and 4.5408 mmol/g (dry fiber) respectively, nearly two times higher than that of AOPAN conventional fibers. Besides, the desorption rate of Cu²⁺ and Cd²⁺ from metal chelated AOPAN nanofibers was 87 and 92 % respectively in 1 mol/l nitric acid solution for 60 min. The isothermal processes were found to be in conformity with Langmuir model.     

Synthesis and application of ramie fiber soft modifier comprised of carboxylate-containing polymer

In effort to improve the soft properties of ramie fiber, we synthesized a carboxylate-containing polymer for use as a modifying agent, and successfully modified the ramie fiber in a strong base with the carboxylate-containing polymer. We applied Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), thermogravimetric analysis (TGA), and scanning electron microscopy (SEM) to investigate the structures of the raw and modified ramie fibers, and further investigated the mechanical and dyeing properties of the raw and modified ramie fibers. The results showed that the surface of the ramie fiber underwent significant changes due to the grafting reaction of the carboxylate-containing polymer and fiber. After the chemical modification, the flexural strength and initial modulus of the modified ramie fiber decreased while tensile strength increased, indicating that the softness of the modified ramie fiber increased though its tensile resistance remained high. In addition, the fixation of reactive dyes on the modified ramie fiber was larger than that of the reactive dyes on the raw ramie fiber. Our observations of mechanical properties and dye fixation indicated that the carboxylate-containing polymer is an effective and efficient soft modifier.     

Fique fibers: Enhancement of the tensile strength of alkali treated fibers during tensile load application

Fique fibers were treated using Na(OH) solution at 5 w/v%, slack and under 1 N of tension, at room temperature, for 4 and 24 h respectively. Changes in their structure and composition were monitored using Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA) and X-ray diffraction (XRD). Additionally their mechanical properties were evaluated and analyzed. Results showed that tensile load application during alkali treatment improves their tensile strength and modulus. The most important change in mechanical properties was achieved in fibers treated for 24 h under tension. However, these fibers presented a high standard deviation; due to this treatment causing an important defibrillation. Moreover, fibers treated for 4 hours under tension, enhance their tensile strength around 56 %, while slack treated fibers improve only 38 %. When fibers were treated under tension, cellulose microfibrills were rearranged in the direction of tensile application and the spiral angle decreased, increasing the molecular orientation.     

Macro-micro structure,antibacterial activity,and physico-mechanical properties of the mulberry bast fibers

In this paper, the mulberry fibers were successfully obtained by a new pretreatment named alkali-assisted microwave plus biological enzymatic technique (AMBET). The morphology, microstructure, physico-mechanical and antibacterial properties of the mulberry bast fibers were investigated by means of scanning electron microscope (SEM), Fourier Transform-Infrared (FTIR), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), X-ray diffraction (XRD), instron tensile tester and antibacterial testing. The results showed that impurities of the bast fibers could be removed by AMBET treatment. AMBET treated mulberry fiber was even, smooth and fine, and typical cellulose I in the mulberry fibers was confirmed by FTIR and XRD analysis. The crystallinity of the AMBET treated fibers was higher than that of the raw mulberry and chemical treated mulberry fibers. Thermal analysis indicated that the mulberry fibers had a good thermal stability. Moreover, the AMBET treated mulberry fibers showed excellent antimicrobial activities against S.aureus. The physical properties of the mulberry fibers indicated the AMBET treated mulberry fibers were ideal candidates for new textile materials.     

Modification of polyacrylonitrile precursor fiber with hydrogen peroxide

Polyacrylonitrile (PAN) precursor fibers were modified for different periods of time using hydrogen peroxide aqueous solution. A variety of tests were employed to characterize the fibers. The modification could induce cyclization and oxidation in the precursor fibers, as reflected by the changes in length and diameter of the fibers, and the results of Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). Compared with the unmodified fiber, the modified fibers released less heat during a heating process similar to stabilization of PAN precursor fiber. Also, the modified fibers showed lower characteristic temperatures on differential scanning calorimetry (DSC) thermograms, and lower onset temperature of weight loss on thermal gravimetry (TG) curves. The modified fibers had more surface defects and hence exhibited lower tenacity and tensile modulus. Compared with the unmodified fibers, however, the modified fibers had smoother surface and fewer defects after stabilization. The strain decreased with increasing temperature under a constant tension for all the fibers. At the temperatures above 200 °C, the shrinkage of the fibers decreased with the increase of modification time, because a certain degree of cyclization and oxidation occurred in modified fibers, making them shrink less in the temperature range equivalent to stabilization.