Manufacturing silk/epoxy composite laminates : challenges and opportunities

Presented at the 34th International Conference of the Polymer Processing Society, May 24, 2018.Application of natural fibers in polymer composites has been gaining popularity in several industries pursuing environmentally friendly products. Among the natural fibers with proven potential applications, silk fibers have recently received considerable attention from researchers. Silk fibers provide higher mechanical properties compared to other commonly used natural fibers such as sisal, jute, and hemp. Silk may also exhibit comparable specific mechanical properties to glass fibers. However, silk composite laminates are rarely used in commercial products due to a number of fabrication challenges. This paper investigates such challenges for silk/epoxy laminates, especially issues related to manufacturing and preform architecture. First, challenges arising from preform architecture (i.e., random and woven preforms) are presented. Unlike glass fibers for which random mats are easier to manipulate, handling random silk preform proves to be more challenging, particularly compared to woven silk fabrics. The random silk/epoxy laminates show higher thickness variation and lower compaction, yielding lower fiber content. Second, fabrication of laminates by vacuum bag/wet lay-up and vacuum assisted resin transfer molding (VARTM) processes are presented. VARTM is found to be more appropriate for silk/epoxy laminate fabrication, as it allows a uniform impregnation of the silk preform, yielding higher part quality and limited void formation. Moreover, applying 0.21 MPa (30 psi) external pressure to the VARTM laminates allows to increase the fiber content of both random and woven silk/epoxy laminates from ~17 and ~30% to ~21 and ~33%, respectively. In contrast, wetting of silk preform during wet lay-up process, which is operator dependent, is difficult to achieve; and the produced laminates have high void content. Furthermore, SEM images show a weak silk/epoxy adhesion in laminates fabricated without external pressure. Finally, the mechanical performance of these laminates is assessed. The woven silk/epoxy laminates fabricated by pressurized VARTM exhibits the highest improvement in the specific flexural strength and modulus over pristine epoxy with 30 and 65% increase, respectively.YesPeer reviewed for the Proceedings of the 34th International Conference of the Polymer Processing Society, Taipei, Taiwan, May 21st-25th 2018

Silk as a Natural Reinforcement: Processing and Properties of Silk/Epoxy Composite Laminates

With growing environmental awareness, natural fibers have recently received significant interest as reinforcement in polymer composites. Among natural fibers, silk can potentially be a natural alternative to glass fibers, as it possesses comparable specific mechanical properties. In order to investigate the processability and properties of silk reinforced composites, vacuum assisted resin transfer molding (VARTM) was used to manufacture composite laminates reinforced with woven silk preforms. Specific mechanical properties of silk/epoxy laminates were found to be anisotropic and comparable to those of glass/epoxy. Silk composites even exhibited a 23% improvement of specific flexural strength along the principal weave direction over the glass/epoxy laminate. Applying 300 kPa external pressure after resin infusion was found to improve the silk/epoxy interface, leading to a discernible increase in breaking energy and interlaminar shear strength. Moreover, the effect of fabric moisture on the laminate properties was investigated. Unlike glass mats, silk fabric was found to be prone to moisture absorption from the environment. Moisture presence in silk fabric prior to laminate fabrication yielded slower fill times and reduced mechanical properties. On average, 10% fabric moisture induced a 25% and 20% reduction in specific flexural strength and modulus, respectively

Three-dimensional nano-morphology of carbon nanotube/epoxy filled poly(methyl methacrylate) microcapsules

HAMIDI, Youssef K./0000-0003-3648-9939WOS: 000469757500028PubMed: 31035448The three-dimensional nano-morphology of poly(methyl methacrylate; PMMA) microcapsules filled with carbon nanotubes (CNTs) and epoxy resin were investigated by various microscopy methods, including a novel, laser scanning confocal microscopy (LSCM) method. Initially, PMMA microcapsules containing various amounts of CNTs were synthesized by a solvent evaporation method. Scanning electron microscopy analysis showed that pore-free, smooth-surface microcapsules formed with various types of core-shell morphologies. The average size of CNT/epoxy/PMMA microcapsules was shown to decrease from similar to 52 m to similar to 15 m when mixing speed during synthesis increased from 300 rpm to 1000 rpm. In general, the presence of CNTs resulted in slightly larger microcapsules and higher variations in size. Moreover, three-dimensional scans obtained from confocal microscopy revealed that higher CNT content increased the occurrence and size of CNT aggregates inside the microcapsules. Entrapped submicron air bubbles were also observed inside most microcapsules, particularly within those with higher CNT content