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Large tow carbon fiber (LTCF) has excellent performance and low cost. However, there are still many difficulties in the application of LTCFs, among which the problem of interfacial penetration is mainly solved. Building interfaces with sizing structures of fiber composites is an effective approach to achieve high performance. In this article, a water-based epoxy sizing agent suitable for LTCF fiber thermoset composites was studied. A comparison of the five LTCFs in this study shows that the wettability and contact angle of the sized LTCFs are significantly improved. In addition, the interfacial shear strength (IFSS) and interlaminar shear strength (ILSS) increased from 52.3 to 71.0 MPa (35%) and 36.4 to 54.6 MPa (50%), respectively. Compared with other imported LTCFs, domestic large-size LTCFs have a wide variety and a large number of surface functional groups, thereby improving their wettability and covalent bonding with the resin matrix. This work has reference significance for the practical application and industrial production of LTCFRP. [ABSTRACT FROM AUTHOR]

To satisfy the light weight requirements of vehicles owing to the aggravation of environmental pollution, carbon-fiber (CF)-reinforced epoxy composites have been chosen as a substitute for traditional metal counterparts. Since the current processing methods such as resin transfer molding (RTM) and compression molding (CM) have many limitations, an integrated and optimal molding method needs to be developed. Herein, we prepared high-performance composites by an optimized molding method, namely compression resin transfer molding (CRTM), which combines the traditional RTM and CM selectively and comprehensively. Differential scanning calorimetry (DSC) and rotational rheometry were performed to optimize the molding parameters of CRTM. In addition, metallurgical microscopy test and mechanical tests were performed to evaluate the applicability of CRTM. The experimental results showed that the composites prepared by CRTM displayed superior mechanical properties than those of the composites prepared by RTM and CM. The composite prepared by CRTM showed up to 42.9%, 41.2%, 77.3%, and 5.3% increases in tensile strength, bending strength, interlaminar shear strength, and volume fraction, respectively, of the composites prepared by RTM. Meanwhile, the porosity decreased by 45.2 %. [ABSTRACT FROM AUTHOR]

In this work, a dicyclopentadiene monomer/Grubbs 2 catalyst was added to a mixture of epoxy oligomers and methyl nadic anhydride to obtain a poly‐dicyclopentadiene (DCPD) modified epoxy cross‐linked network via sequential curing. The hybrid resin was used as a matrix for preparing carbon fiber composites. The results indicated that the addition of DCPD monomers significantly reduced the viscosity of the epoxy resin. The toughness and heat resistance of the co‐cured resin was improved without significant loss of strength, which was attributed to the high compatibility between epoxy and the modifier polymer. Regarding the composites, the flexural strength of the hybrid resin‐derived composite first increased and then diminished slightly. Meanwhile, the mode‐I interlaminar fracture toughness continued to increase with the increase of PDCPD content compared to the non‐modified composites. Generally, the change trend of the above properties in the composites was consistent with the change trend of the strength and toughness exhibited in the bulk resin with increasing PDCPD contents, while the change extent was inconsistent due to factors such as fiber volume content and interfacial bonding. Highlights: The epoxy/PDCPD hybrid resin system was obtained via sequential curing.The PDCPD as modifier can reduce the viscosity of the epoxy curing system.The toughness and heat resistance of the PDCPD modified epoxy resin was improved.The loss in flexural strength of the hybrid resin system was insignificant.The GIC of the epoxy composites modified with PDCPD improved appreciably. [ABSTRACT FROM AUTHOR]

In this work, the tackified PDCPD (PDCPD-T) specialized for vacuum assistant resin infusion process (VARI) was developed. The epoxy resin and methyl nadic anhydride (NMA) was subsequently added to the PDCPD-T to improve the interfacial bonding with the carbon fibres. The results showed that the introduction of NMA-cured epoxy undermined the mechanical properties of the PDCPD-T owing to the agglomeration of the tackifier particles. Nonetheless, the mechanical properties of the CFRCs based on the co-cured blends of the PDCPD-T and the NMA-cured epoxy were comprehensively improved compared to the composites based on the PDCPD-T. The improvement was that a part of NMA-cured epoxy in the co-cured blends would phase separate on the surface of the carbon fibre, which formed the "bridge" connecting the matrix and the carbon fibre. In addition, the degree of the tackifier agglomeration would also decrease due to the decrease in the surrounding epoxy concentration. [Display omitted] • The continuous carbon fiber reinforced polydicyclopentadiene (PDCPD) composites based on the vacuum-assisted resin infusion process are realized by tackifying the dicyclopentadiene (DCPD) monomer. • The further addition of anhydride-cured epoxy resin to the tackified DCPD monomer solves the problem of poor interfacial bonding between the PDCPD resin and the carbon fiber. • The carbon fiber composites based on the modified PDCPD matrix are proved to be far superior in interlaminar fracture toughness and impact resistance than the epoxy-based composites. [ABSTRACT FROM AUTHOR]