Bend,Twist, and Turn: First Bendable and Malleable Toughened PLA Green Composites

The future of green electronics possessing great strength and toughness proves to be a promising area of research in this technologically advanced society. This work develops the first fully bendable and malleable toughened polylactic acid (PLA) green composite by incorporating a multifunctional polyhydroxybutyrate rubber copolymer filler that acts as an effective nucleating agent to accelerate PLA crystallization and performs as a dynamic plasticizer to generate massive polymer chain movement. The resultant biocomposite exhibits a 24‐fold and 15‐fold increment in both elongation and toughness, respectively, while retaining its elastic modulus at >3 GPa. Mechanism studies show the toughening effect is due to an amalgamation of massive shear yielding, crazing, and nanocavitation in the highly dense PLA matrix. Uniquely distinguished from the typical flexible polymer that stretches and recovers, this biocomposite is the first report of PLA that can be “bend, twist, turn, and fold” at room temperature and exhibit excellent mechanical robustness even after a 180° bend, attributes to the highly interconnected polymer network of innumerable nanocavitation complemented with an extensively unified fibrillar bridge. This unique trait certainly opens up a new horizon to future sustainable green electronics development.     

Preparation and characterization study on maleic acid cross-linked poly(vinyl alcohol)/chitin/nanocellulose composites

In the quest on improving composite formulations for environmental sustainability, maleic acid (MA) cross-linked poly(vinyl alcohol) (PVA)-α-chitin composites reinforced by oil palm empty fruit bunch fibers (OPEFB)-derived nanocellulose crystals (NCC) had been successfully prepared. Based on the Fourier transform infrared (FTIR) spectroscopic analysis, it was proven that molecular interactions of the cross-linker to the polymeric networks was through conjugated ester linkage. Differential scanning calorimetry (DSC) showed that the influence of MA was minimal toward crystallization in the PVA/chitin/NCC composite. Maximum tensile strength, elongation at break and Young's modulus of the respective PVA/chitin/NCC composites were achieved at different content of MA, dependent on the PVA/chitin mass ratio. Among all compositions, a maximum Young's modulus was achieved at 30 wt% MA loading in PVA/chitin-30/NCC, amounting to 2,413.81 ± 167.36 MPa. Moreover, the mechanical properties and selected physicochemical properties (swelling, gel content, and contact angle) of the PVA/chitin/NCC composites could be tailored by varying the chitin content (10–30 wt%) and MA content (10–50 wt% based on total mass of composite). In brief, this chemically cross-linked PVA-based biocomposites formulated with sustainable resources exhibited tunable physicochemical and mechanical properties.     

Formulation and Characterization of Novel Nanostructured Lipid Carriers with Photoprotective Properties Made from Carnauba Wax,Beeswax, Pumpkin Seed Oil,and UV Filters

Pumpkin seed oil (PSO) with carnauba wax and beeswax was used to develop nanostructured lipid carriers (NLC) loaded with a UV filter, Uvinul® A Plus B. The aims of the study were to optimize the concentration of PSO to develop a stable NLC formulation, determine storage stability of the NLC with and without PSO, and the synergistic effect of PSO-NLC with UV filter for photoprotective properties. The physical properties of NLC were optimized based on the mean particle size, polydispersity index, and storage stability. The optimized NLC consisted 10% lipid phase (3.5% carnauba wax, 3.5% beeswax, and 3.0% PSO) and 90% aqueous phase. After optimization, Uvinul® A Plus B was added in the optimized PSO-NLC to produce a photoprotective formulation. Uvinul® A Plus B consisted of both UVA (Diethylamino Hydroxybenzoyl Hexyl Benzoate) and UVB (Ethylhexyl Methoxycinnamate) filters. The NLC produced with PSO and Uvinul® A Plus B had mean particle size of 135 ± 2 nm and showed good physical stability under storage time. Besides that, the NLC produced also proven to have positive effect in enhancing the entrapment efficiency and drug loading, which were 82.86 ± 0.15% and 55.41 ± 0.04%, respectively, and showed sun protection factor value of 16.61 ± 3.45. The results indicated the presence of synergistic effect among the PSO-NLC with Uvinul® A Plus B.     

Affixing poly(methyl methacrylate-co-acrylic acid) nanospheres with trimethoxyvinylsilane on silicon solar module to enhance its power conversion efficiency

Poly(methyl methacrylate-co-acrylic acid) [P(MMA-co-AA)] incorporated with 0–9 wt% of trimethoxyvinylsilane (TMVS) has been studied to investigate the effect of TMVS on the adhesion properties of P(MMA-co-AA) nanospheres coated on silicon substrate as well as on the power conversion efficiency (PCE) of silicon solar module coated with the polymer nanospheres. The incorporation of 7 and 9 wt% of TMVS into the copolymer has been found to render the copolymer stronger adhesion to glass substrate than the samples with lower amount of TMVS in them. The coating of the P(MMA-co-AA) nanospheres on the glass surface of solar module increases the light harvesting efficiency by serving as an anti-reflective layer. Solar module coated with an array of P(MMA-co-AA) nanospheres with 7 wt% of TMVS yielded the highest PCE enhancement of 98% under the illumination of an AM1.5 solar simulator. The natural weathering results indicate that the copolymer with 7% of TMVS was able to withstand prolonged natural weathering exposure and remained reasonably effective in PCE enhancement up to 130 days of outdoor exposure. This study demonstrates a cost-effective technique to bind [P(MMA-co-AA)] nanospheres onto the silicon surface of solar module via siloxane linkages and thus increases the PCE of the solar module effectively. The T_g of the copolymer increased linearly from 110.31 to 118.42 °C when 0–9 wt% of TMVS was added into it. Thermogravimetry results indicate that the incorporation of TMVS does not give any significant effect on the T_d of the copolymer, which occurs at about 390 °C.

     

Electrochemical conversion of switchgrass and poplar in molten carbonate direct carbon fuel cell

One way of sustaining fuel cell technology is using renewable and sustainable energy means provided by biomass. This article explores switchgrass and poplar in a molten carbonate electrolyte direct carbon fuel cell. It investigates their electrochemical conversions and provides results of power density, current density, open circuit voltage (OCV) and other parameters. The biomasses were pyrolysed at 800°C to produce carbon fuels. Biomass carbon fuels were mixed with molten carbonate and subjected to different operating conditions (600–800°C) in the fuel cell. The electrochemical performances of the poplar fuel were better than those experienced with switchgrass fuel. At 800°C the OCV of poplar fuel (1.08?V) has higher output than switchgrass (0.87?V). The peak power density recorded for poplar fuel was 23.91?mW/cm² while switchgrass fuel was lower at 21.60?mW/cm². Poplar fuel (81.53?mA/cm²) gave a maximum current density with switchgrass fuel lower at 74.00?mA/cm².     

Synthesis of graphene/vitamin C template-controlled polyaniline nanotubes composite for high performance supercapacitor electrode

A graphene nanosheet/polyaniline nanotube (GPNT) composite is prepared for the first time by in-situ chemical oxidative polymerization of aniline using vitamin C as a structure directing agent. The vitamin C molecules lead to the synthesis of polyaniline (PANI) nanotubes through the development of rod-like assembly by H-bonding in an aqueous medium. The initially synthesized graphene oxide/polyaniline nanotubes composite is reduced to graphene using hydrazine monohydrate followed by re-oxidation and protonation of the PANI to produce the GPNT nanocomposite. This novel composite showed a high specific capacitance of 534.37 F/g and an excellent energy density of 74.27 Wh/kg at a constant current of 0.5 mA. Besides, the GPNT composite exhibited excellent cycle life with 91.4% specific capacitance retained after 500 charge-discharge cycles. The excellent performance is due to the synergistic combination of graphene which provides good electrical conductivity and mechanical stability, and PANI nanofiber which deals with good redox activity.     

Superabsorbent polymer prepared using carboxymethyl cellulose derived from Ceiba pentandra (L.) Gaertn. (kapok) cotton

Superabsorbent polymers (SAPs) were synthesized by grafting acrylic acid and butyl acrylate onto carboxymethyl cellulose (CMC) modified from Ceiba pentandra (L.) Gaertn. (kapok) cotton, with N,N′‐methylenebisacrylamide as a crosslinker and ammonium persulphate as initiator. The effect of distilled water, saline solution, and applied pressure on superabsorbent was investigated. The product exhibited the maximum water absorbency of 554 g/g in distilled water and 96 g/g in saline solution. The SAP achieved the highest water absorbency under load of 83 g/g under applied pressure of 7.6 g/cm². The kapok cotton modified cellulose‐based SAP exhibited stronger gel strength than the SAP based on commercial CMC. This is probably due to the higher grafting efficiency (78.3%) of the former. The SAP was characterized by FTIR analysis, thermogravimetric analysis, and scanning electron microscopy. Thermogravimetric analysis results showed that the SAP, with AA and BA grafted onto CMC, had better thermal stability than CMC alone. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40808.