Poly (p-phenylene terephthalamide) fibers prepared by wet or dry-jet wet spinning processes have a notable response to very brief heat treatment (seconds) under tension. The modulus of the as-spun fiber can be greatly affected by the heat treatment conditions (temperature, tension and duration). The crystallite orientation and the fiber modulus will increase by this short-term heating under tension. Poly (p-phenylene terephthalamide) fibers have a very high molecular orientation (orientation angle 12-20°). Kevlar  and Twaron  fibers are poly (p-phenylene terephthalamide) fibers. This review reports for PPTA fibers the heat treatment techniques, devices and its process conditions. It reports in details the structural relationships between the fiber properties which are influenced by the heat treatment process. In particular, focused deeply on the effect of the crystal structure and the morphology of the fibers on the mechanical properties of PPTA fibers.

Thermal pre-oxidation of polyacrylonitrile (PAN) fibers is a time-consuming and energy-consuming step in the production of PAN-based carbon fibers. In this paper, the effect of temperature on the structures and properties of PAN fibers cyclized in the supercritical carbon dioxide (Sc-CO2) medium was studied. The thermal behaviors of the PAN fibers were investigated by Fourier transform infrared spectra (FT-IR), X-ray diffraction (XRD), differential scanning calorimeter (DSC) and thermogravimetric analysis (TGA). The cyclization reaction was sensitive to the heating temperature and gas atmosphere. The FT-IR results of the PAN fibers treated in the Sc-CO2 confirmed that the degree of cyclization increased with the increase of the cyclization temperature. Compared with the PAN fibers treated in the air, the PAN fibers treated in the Sc-CO2 showed a higher degree of cyclization even at the same temperature. These findings might be related to the osmotic action of Sc-CO2 causing the fibers to be further arranged in a regular manner, which was favorable for the cyclization reaction. Moreover, as one kind of high diffusion and high heat transfer media, the heat release during the cyclization of PAN fibers could be quickly removed by Sc-CO2, which achieved the progress of the rapid-entry cyclization reaction.

Improving the tensile strength and modulus of aramid fibers by enhancement of the amorphous phase in supercritical carbon dioxide.

No abstract

The effect of supercritical carbon dioxide (ScCO 2 ) treatment with acetic anhydride (AA) for Kevlar fabric on the interfacial adhesion and mechanical properties of Kevlar fabric/epoxy composites was investigated. ScCO 2 treatment with AA remarkably affects the interfacial adhesion, thus improving mechanical properties. The effects of treating time on the surface modification and mechanical properties of composites were studied. Results demonstrated that the optimal condition is 100 C at 10 MPa for 60 min, as shown by the tensile strength and shear strength of the ScCO 2 -treated composites being 21.3 and 47.9% higher than those of the untreated ones, respectively. The mechanical properties demonstrated that ScCO 2 treatment provides an efficient and environmentally safe method for surface modification to improve interfacial interaction between the treated fiber and matrix with ScCO 2 treatment. POLYM. COMPOS., 40: E920-E927, 2019. POLYMER COMPOSITES-2019 FIG. 4. SEM images of the surfaces of Kevlar fiber (a) Kevlar untreated, (b) treating time of 30 min, (c) 60 min, and (d) 90 min. E924 POLYMER COMPOSITES-2019 DOI 10.1002/pc FIG. 7. SEM images of interlaminar shear ruptures of Kevlar fiber/epoxy Kevlar untreated, (b) treating time of 30 min, (c) 60 min, and (d) 90 min E926 POLYMER COMPOSITES-2019

In this work, the layer-by-layer self-assembly technology was used to modify aramid fibers (AFs) to improve the interfacial adhesion to epoxy matrix. By virtue of the facile layer-by-layer self-assembly technique, poly(l-3,4-Dihydroxyphenylalanine) (l-PDOPA) was successfully coated on the surface of AFs, leading to the formation of AFs with controllable layers (nL-AF). Then, a hydroxyl functionalized silane coupling agent (KH550) was grafted on the surface of l-PDOPA coated AFs. The properties such as microstructure and surface morphology of AFs before and after modification were characterized by FTIR, XPS and FE-SEM. The results confirmed that l-PDOPA and KH550 were successfully introduced into the surface of AFs by electrostatic adsorption. The interfacial properties of AFs reinforced epoxy resin composites before and after coating were characterized by interfacial shear strength (IFSS), interlaminar shear strength (ILSS) and FE-SEM, and the results show that the interfacial adhesion properties of the modified fiber/epoxy resin composites were greatly improved.

Aramid fibers with low density and high strength, modulus, and thermal resistance are widely used in applications such as bulletproof vests and cables. However, owing to their chemical structure, they are sensitive to ultraviolet light, which degrades the fibers’ useful mechanical properties. In this study, titanium dioxide (TiO2) nanoparticles were synthesized both on the aramid III fiber surface and in the interfacial space between the fibrils/microfibrils in supercritical carbon dioxide (scCO2) to improve the UV resistance of aramid fibers. The effects of scCO2 treatment pressure on the TiO2 structure, morphology, surface composition, thermal stability, photostability, and mechanical properties were investigated using Fourier transform infrared spectroscopy, X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy, thermogravimetric analysis, ultraviolet–visible spectroscopy, and single-fiber test. The results show that amorphous TiO2 formed on the fiber surface and the interface between fibrils/microfibrils, and decreased the photodegradation rate of the aramid III fiber. Moreover, this modification can also improve the tensile strength via treatment at low temperature and without the use of a solvent. The simple synthesis process in scCO2, which is scalable, is used for mild modifications with a green solvent, providing a promising technique for synthesizing metal dioxide on polymers.

Aramid pulp (AP) is a highly fibrillated form of fiber， with excellent heat resistance, wear resistance, size stability, and other beneficial properties, that can be dispersed in rubber or resin matrix systems. Its fibrillation results in a large surface area. However, AP easily tangles and aggregates between fibers because of its large surface area. Consequently, it experiences difficulty in dispersing in matrices, especially when a relatively large amount of pulp is needed to be mixed. In this study, a SiO2 nanoparticle was synthesized on the surface of AP through the hydrolysis of tetraethyl orthosilicate to improve the dispersion of AP in an epoxy matrix. Fourier transform infrared spectroscopy, X‐ray diffraction, thermogravimetric analysis, X‐ray photoelectron spectroscopy, and scanning electron microscopy showed that SiO2 nanoparticles coated on the pulp could improve the thermal and mechanical properties. The optimum treatment concentration was 0.15 mol/L. Dynamic mechanical analysis tests indicated when AP modified by SiO2, the E' is higher due to the uniformly diffusion and enhanced interfacial adhesion for load transfer from the epoxy to AP. But Tg is lower as the flexibility chain SiOSi in epoxy. In comparison with the properties of the unmodified AP, the tensile strength and modulus of modified pulp/epoxy composites increased by 53.5% and 160.4%, respectively. Therefore, the dispersion and interface combination of AP modified by SiO2 in the epoxy improved because of the interaction of AP with SiO2 through the hydrogen bonding and crosslinking of SiO2 with epoxy.