This study focused on exploring the feasibility of green composites made from biodegradable and renewable materials as potential alternatives to petroleum polymer composites and understanding the reinforcing mechanisms in composites containing kenaf fibers (KF). KF-reinforced poly(lactide) acid (PLA) composites were made using melt compounding and injection molding, and their properties were compared to that of KF-reinforced polypropylene (PP) composites. The flexural properties and thermomechanical behavior were determined as a function of the fiber content, the crystallization of PLA and PP was studied using X-ray diffraction and differential scanning calorimetry, and the composites’ morphology was investigated using scanning electron microscopy. It was concluded that PLA exhibits higher modulus and Tg compared to those of neat PP. The modulus of the composites at 40 wt% fibers is 6.64 GPa and 2.96 GPa for PLA and PP, respectively. In general, addition of kenaf results in larger property enhancement in PP due to better wetting of the fibers by the low melt viscosity PP and the crystallization behavior of PP that is significantly altered by the fibers. The novelty of this work is that it provides one-to-one comparison of PLA and PP composites, and it explores the feasibility of fabricating green composites with enhanced properties using a simple scalable process.
Advanced carbon materials are important for the next-generation of energy storage apparatus, such as electrochemical capacitors. Here, the physical and electrochemical properties of carbonised filter paper (FP) were investigated. FP is comprised of pure cellulose and is a standardised material. After carbonisation at temperatures ranging from 600 to 1700 °C, FP was contaminant-free, containing only carbon and some oxygenated species, and its primary fibre structure was retained (diameter ≈20–40 μm). The observed enhancement in conductivity of the carbonised FP was correlated with the carbonisation temperature. Electrochemical capacitance in the range of ≈1.8–117 F g−1 was achieved, with FP carbonised at 1500 °C showing the best performance. This high capacitance was stable with >87 % retained after 3000 charge–discharge cycles. These results show that carbonised FP, without the addition of composite materials, exhibits good supercapacitance performance, which competes well with existing electrodes made of carbon-based materials. Furthermore, given the lower cost and renewable source, cellulose-based materials are the more eco-friendly option for energy storage applications.
This study compared the dynamic mechanical and thermal properties of biocomposites reinforced with algae fiber; polypropylene (PP) and poly(lactic acid) (PLA) biocomposites. The biocomposites are manufactured with a bleached red algae fiber (BRAF) loading ranging from 30 to 60 wt%. The thermal properties of BRAF, PLA and PP were determined by DSC and TGA. The dynamic mechanical and thermomechanical properties of the PLA matrix and biocomposites were analyzed by DMA and TMA. The dynamic mechanical and thermomechanical properties of both BRAF/PLA and BRAF/PP biocomposites show improvement with increasing BRAF loading. The fibers were well bonded with the PLA matrix, indicating strong adhesion, as observed by SEM observations of the fractured surface. In addition, greater improvement in the storage modulus was achieved with the BRAF/PLA biocomposites than with the BRAF/PP biocomposites. Therefore, BRAF/PLA biocomposites can be used as an alternative completely biodegradable biocomposite to BRAF/PP biocomposites.
Nanofibers composed of cellulose acetate (CA) and montmorillonite (MMT) were prepared by electrospinning method. MMT was first dispersed in water and mixed with an acetic acid solution of CA. The viscosity and conductivity of the CA/MMT solutions with different MMT contents were measured to compare with those of the CA solution. The CA/MMT solutions were electrospun to fabricate the CA/MMT composite nanofibers. The morphology, thermal stability, and crystalline and mechanical properties of the composite nanofibers were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDX), thermogravimetric analysis (TGA), X-ray diffraction (XRD), and tensile test. The average diameters of the CA/MMT composite nanofibers obtained by electrospinning 18 wt% CA/MMT solutions in a mixed acetic acid/water (75/25, w/w) solvent ranged from 150~350 nm. The nanofiber diameter decreased with increasing MMT content. TEM indicated the coexistence of CA nanofibers. The CA/MMT composite nanofibers showed improved tensile strength compared to the CA nanofiber due to the physical protective barriers of the silicate clay layers. MMT could be incorporated into the CA nanofibers resulting in about 400% improvement in tensile strength for the CA sample containing 5 wt% MMT.
Advanced carbon materials formed from abundant biomass are an exciting and promising class for energy devices due to the clear advantages of low cost, sustainability and good physical and electrochemical properties. However, these materials typically do not compete well with their metal functionalised counterparts. In this work, we demonstrate that xCo(OH) 2 -(1−x)Ni(OH) 2 with various Ni:Co ratios can be deposited onto biomass-derived carbon to make a hybrid inorganic-carbon electrode with tuneable physical features and electrochemical performance. These features were tuned by adjusting the Ni:Co ratio within precursor solutions. The electrodes had shown a capacitance ranging from 780.7 to 2041 F g −1 , which is very close to the theoretical value for Ni(OH) 2 (2365 F g −1 ). A hypothesis is presented to help explain this performance for a modified, biomass-derived carbon electrode.
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