Improved interfacial performance of carbon fiber/polyetherimide composites by polyetherimide and modified graphene oxide complex emulsion type sizing agent

In the field of interfacial enhancement of composite, sizing method has attracted extensive attention. In this research, a new complex emulsion type sizing agent containing polyetherimide (PEI) and covalently chemical functionalized graphene oxide (GO) was first proposed to further improve the interfacial adhesion of carbon fiber (CF)/PEI composites, adapt to the high processing temperature, and overcome the shortcomings of the solution type sizing agent. The emulsion was prepared by the emulsion/solvent evaporation method. In order to avoid the agglomeration of nanomaterials on CF surface, the monomer and polymer structure of PEI was used to functionalize GO, so as to achieve better compatibility and dispersion of GO in PEI. The physicochemical state of CF surface was characterized and the successful introduction of GO was verified. The microbond test revealed that the introduction of GO further improved the IFSS compared with only PEI sizing. When GO grafted with PEI was used as the main component of the sizing agent, the IFSS reached the largest with an increasement of 55.96%. The mechanism of interfacial reinforcement was proposed. Increased ability of mechanical interlocking, the mutual solubility between PEI molecular chains, and the improvement in wettability may be beneficial to the interfacial strength. This mild and effective modification method provided theoretical guidance for the interfacial enhancement of composites and was expected to be applied in industrial production.

Shock-Induced Damage Mechanism of Perineuronal Nets

The perineuronal net (PNN) region of the brain’s extracellular matrix (ECM) surrounds the neural networks within the brain tissue. The PNN is a protective net-like structure regulating neuronal activity such as neurotransmission, charge balance, and action potential generation. Shock-induced damage of this essential component may lead to neuronal cell death and neurodegenerations. The shock generated during a vehicle accident, fall, or improvised device explosion may produce sufficient energy to damage the structure of the PNN. The goal is to investigate the mechanics of the PNN in reaction to shock loading and to understand the mechanical properties of different PNN components such as glycan, GAG, and protein. In this study, we evaluated the mechanical strength of PNN molecules and the interfacial strength between the PNN components. Afterward, we assessed the PNN molecules’ damage efficiency under various conditions such as shock speed, preexisting bubble, and boundary conditions. The secondary structure altercation of the protein molecules of the PNN was analyzed to evaluate damage intensity under varying shock speeds. At a higher shock speed, damage intensity is more elevated, and hyaluronan (glycan molecule) is most likely to break at the rigid junction. The primary structure of the protein molecules is least likely to fail. Instead, the molecules’ secondary bonds will be altered. Our study suggests that the number of hydrogen bonds during the shock wave propagation is reduced, which leads to the change in protein conformations and damage within the PNN structure. As such, we found a direct connection between shock wave intensity and PNN damage.

Atomistic-scale analysis of the deformation and failure of polypropylene composites reinforced by functionalized silica nanoparticles

Interfacial adhesion between polymer matrix and reinforcing silica nanoparticles plays an important role in strengthening polypropylene (PP) composite. To improve the adhesion strength, the surface of silica nanoparticles can be modified by grafted functional molecules. Using atomistic simulations, we examined the effect of functionalization of silica nanoparticles by hexamethyldisilazane (HMDS) and octyltriethoxysilane (OTES) molecules on the deformation and failure of silica-reinforced PP composite. We found that the ultimate tensile strength (UTS) of PP composite functionalized by OTES (28 MPa) is higher than that of HMDS (25 MPa), which is in turn higher than that passivated only by hydrogen (22 MPa). To understand the underlying mechanistic origin, we calculated the adhesive energy and interfacial strength of the interphase region, and found that both the adhesive energy and interfacial strength are the highest for the silica nanoparticles functionalized by OTES molecules, while both are the lowest by hydrogen. The ultimate failure of the polymer composite is initiated by the cavitation in the interphase region with the lowest mass density, and this cavitation failure mode is common for all the examined PP composites, but the cavitation position is dependent on the tail length of the functional molecules. The present work provides interesting insights into the deformation and cavitation failure mechanisms of the silica-reinforced PP composites, and the findings can be used as useful guidelines in selecting chemical agents for surface treatment of silica nanoparticles.

Influence of Waste Clinical Mask Fiber on Interfacial Strength Parameters

To investigate the influence of clinical mask fibers on the geotechnical properties of different interfaces. In the present study different geotechnical tests like Triaxial Shear Tests, California Bearing Ratio Tests, and split tensile strength tests were done to understand the behavior of different mix propositions containing clinical mask fiber. From the test result, it is clear that the addition of waste clinical mask fiber in different mix proportions increases the overall shear strength of the material. Also, the percentage increases in CBR value were recorded by about 40% with the addition of clinical mask fiber. In addition, from the split tensile tests results on different mix proportions, it is observed that the tensile strength value increases up to 45% to 50 % with the addition of mask fiber to respective coarser and fine grain compositions. Thus, the study confirms that clinical mask fibers have the potential to improve the geotechnical properties and can be used as fill material in different construction like retaining structures and earthen embankments.

On the tensile fracture behavior of Cr coating for ATF cladding considering the effect of pre-oxidation

In this study, the fracture mechanisms of Cr-coated Zr4 alloy samples were studied by in-situ tensile testing with high-resolution observations. Both original sample and pre-oxidized sample were studied to study the effects of pre-oxidation on the cracking and failure behavior. For the Cr-coated Zr4 sample, with the increase of tensile strain, multiple surface cracks were dominant and less interfacial cracks were formed, indicating good interfacial strength of Cr coating. For the pre-oxidized samples, there was a thin oxide layer formed on the Cr coating surface, revealing improved oxidation resistance and protection effects. However, a brittle ZrCr2 diffusion layer was formed in the same while at the Cr/Zr4 interface underneath the Cr coating, which would lead to earlier micro-cracks formed under tensile stress and evidently degrade the interfacial strength. The findings in the study indicated the importance of optimizing coating microstructure in future study to avoid forming the above-mentioned brittle diffusion interlayer and the associated premature failure.

The Effect of Touch-Cure Polymerization on the Conversion and Hardness of Core Build-Up Resin Composites: A Laboratory Study

To improve the self-curing capacity and interfacial strength with dentine of dual-cured composite materials, touch-cure activators have been introduced. The aim of the study was to evaluate the effect of these activators on the hardness and conversion of dual-cured resin composite core build-up restoratives. The materials tested were Clearfil DC Core Plus (CF) and Gradia Core (GC) with the corresponding adhesives Clearfil S3 Bond Plus (for CF) and G-Premio Bond/G-Premio DCA activator (for GC). Disk-shaped specimens (n = 6/group) were prepared for the following groups: dual-cured, self-cured and self-cured in contact with the adhesive activators at the bottom surface. After a 3-week storage period (dark/dry/37 °C) the Martens hardness (HM) and degree of conversion (DC%) were determined for the previously mentioned groups and the top surfaces of groups in contact with the adhesives. A statistical analysis was performed by a one-way ANOVA and Holm–Sidak test per material and a Pearson’s correlation analysis (HM vs. DC%) at an α = 0.05. The self-cured specimens resulted in significantly lower HM and DC% values from the dual-cured group, as expected. However, in the presence of the adhesives with touch-cure activators, the conversion of the self-cured groups showed insignificant differences in HM and DC% from the dual-cured in both composite materials. The improvements on the bottom composite surfaces in contact with the adhesives did not extend to the entire specimen length. Nevertheless, improved interfacial curing may improve interfacial durability.