Graphene reinforced carbon fibers

The superlative strength-to-weight ratio of carbon fibers (CFs) can substantially reduce vehicle weight and improve energy efficiency. However, most CFs are derived from costly polyacrylonitrile (PAN), which limits their widespread adoption in the automotive industry. Extensive efforts to produce CFs from low cost, alternative precursor materials have failed to yield a commercially viable product. Here, we revisit PAN to study its conversion chemistry and microstructure evolution, which might provide clues for the design of low-cost CFs. We demonstrate that a small amount of graphene can minimize porosity/defects and reinforce PAN-based CFs. Our experimental results show that 0.075 weight % graphene-reinforced PAN/graphene composite CFs exhibits 225% increase in strength and 184% enhancement in Young’s modulus compared to PAN CFs. Atomistic ReaxFF and large-scale molecular dynamics simulations jointly elucidate the ability of graphene to modify the microstructure by promoting favorable edge chemistry and polymer chain alignment.

Nanoscale toughening of ultrathin graphene oxide-polymer composites: mechanochemical insights into hydrogen-bonding/van der Waals interactions, polymer chain alignment, and steric parameters

Systematic molecular dynamics simulations reveal design criteria for utilization of ultra-thin polymer adlayer to toughen monolayer graphene oxide through nanoscale crack-bridging.

Enzymatic degradation of coconut shell powder–reinforced polylactic acid biocomposites

This work examined the effects of filler content and chemical treatment on the biodegradation of poly(lactic acid) (PLA)/coconut shell (CS) biocomposites in a diastase enzyme-containing buffer medium. CS was treated with two distinct chemical treatments: maleic acid and silanation with 3-aminopropyltriethoxysilane (3-APE). The CS was incorporated into PLA composites and their biodegradation patterns were studied. Both of the treated PLA/CS biocomposites exhibited lower biodegradation rates than the untreated biocomposites due to their enhanced interfacial adhesion, which reduced the area exposed to enzyme hydrolysis. Scanning electron micrographs taken after 30 days of biodegradation displayed surface roughening on both of the treated biocomposites, with fewer voids compared to the untreated biocomposites. The differential scanning calorimetry indicated that the glass transition temperature and melting temperature values of the treated biocomposites increased but that crystallinity declined. The crystallization temperature peak apparently disappeared due to the polymer chain alignment and rearrangement of the shorter PLA chains caused by the degradation. Fourier transform infrared analysis revealed the structural changes in the biocomposites after biodegradation, indicating the presence of soluble lactic acid as was confirmed by ultraviolet–visible spectroscopy analysis.

Nanoparticle amount, and not size, determines chain alignment and nonlinear hardening in polymer nanocomposites

Polymer nanocomposites—materials in which a polymer matrix is blended with nanoparticles (or fillers)—strengthen under sufficiently large strains. Such strain hardening is critical to their function, especially for materials that bear large cyclic loads such as car tires or bearing sealants. Although the reinforcement (i.e., the increase in the linear elasticity) by the addition of filler particles is phenomenologically understood, considerably less is known about strain hardening (the nonlinear elasticity). Here, we elucidate the molecular origin of strain hardening using uniaxial tensile loading, microspectroscopy of polymer chain alignment, and theory. The strain-hardening behavior and chain alignment are found to depend on the volume fraction, but not on the size of nanofillers. This contrasts with reinforcement, which depends on both volume fraction and size of nanofillers, potentially allowing linear and nonlinear elasticity of nanocomposites to be tuned independently.