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The purpose of this paper is to investigate the through-thickness stresses of woven glass fiber reinforced polymer (GFRP) composite laminates under combined tensile and shear loading. Tensile tests were carried out with cross specimens at room temperature under various stacking angles, and the through-thickness strength properties of the woven GFRP laminates were evaluated. The failure characteristics of the woven GFRP laminates were also studied by optical microscopy observations. A three-dimensional finite element analysis (FEA) was carried out to calculate the stress distributions in the cross specimens, and the failure conditions of the specimens were examined. The numerically determined interlaminar tensile and shear stresses at failure location were consistent with Hoffman and Mohr-Coulomb failure criteria when the stacking angle was relatively small. This work is the first attempt to quantify the relation between interlaminar tensile and shear strengths of GFRP composite laminates under tensile and shear loading simultaneously using a combined numerical and experimental approach. A method based on finite element stress analysis was developed for estimating the through-thickness strength of the composite laminates using the experimentally determined fracture load and location. The results suggest that the through-thickness strength under combined tensile and shear loading can be determined effectively by this approach for relatively small stacking angles.

Cellulose nanofibers (CNFs) are highly crystalline, fibrous materials with a high aspect ratio of long cellulose molecules linked together with strong hydrogen bonds. These long cellulose molecules are incorporated into hemicellulose and lignin, the cell walls of higher plants. The modulus of elasticity of CNF remains constant between 200 °C and +200 °C. However, the linear coefficient of thermal expansion of cellulose fibers was 0.17 ppm/K, which is comparable to that of quartz glass. Further, CNFs have a thermal conductivity in the same order of magnitude as glass. Therefore, they are promising next-generation fiber owing to the excellent mechanical and thermal properties, sustainability, and biodegradability of CNF. Most studies on using CNFs to increase strength have focused on polymer matrix composites, particularly biodegradable polymers. However, it is difficult to increase the strength of materials using CNFs due to the agglomeration of CNFs. Compared to other composite materials, the uniform dispersion of nanosized CNFs is crucial. This article reports that CNFs may behave not as reinforcing fibers but as cross-linking agents to strengthen the polymer when the amount of CNFs is very small in polymer matrix composites, and the addition of CNFs is also effective in strengthening silk yarn and Ti. The mechanical properties of the ceramic green bodies can be increased using CNFs as an auxiliary agent in ceramic slurry. Moreover, the fabrication of composite materials using CNFs is essential for expanding the CNFs applications.

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Little is known about how the strength of biodegradable polymers changes during decomposition. This study investigated the changes in the tensile properties of polybutylene succinate (PBS) and basalt-fiber (BF)-reinforced PBS (PBS-BF) composite sheets during degradation in bacterial solutions. Seven days after the start of the experiment, the elongation at break of the PBS specimens decreased significantly, and the PBS-BF composite specimens were characterized by barely any change in ultimate tensile strength (UTS) after immersion in the bacteria-free medium for 7 and 56 days. Meanwhile, when immersed in the bacterial solution, the UTS of the PBS-BF composite specimens showed a tendency to decrease after 7 days. After 56 days, the UTS decreased to about half of its value immediately after fabrication. The degradation of the material was attributed to infiltration of the bacterial solution into structurally weak areas, causing decomposition throughout the material.