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Cellulose nanocrystal (CNC) has potential to be used as a reinforcement in polymeric nanocomposites because of their inherent biodegradability, universal accessibility, and superior mechanical properties. The most crucial challenge faced in the nanocomposite production is dispersing the nanoparticles effectively in the polymer matrix, so that the exceptional mechanical properties of the nanoparticles can be transferred to the macroscale properties to the bulk nanocomposites. In this research, a safe, effective and ecofriendly modification was used to functionalize the surface hydroxyl groups of CNC via silane treatment. These modified CNCs were used as reinforcements to prepare poly (ethylene oxide) (PEO)/CNC nanocomposites. The composites were prepared using solvent casting method. The composite properties were evaluated using Fourier Transform Infrared Spectroscopy (FT-IR), Scanning Electron Microscopy (SEM), Thermo-Gravimetric Analysis (TGA), Differential Scanning Calorimetry (DSC), and Dynamic Mechanical Analysis (DMA). The SEM micrographs demonstrated that the composites incorporated with silane treated CNCs showed improvement in the dispersion behavior of the nanoparticles in the matrix. Oxidative combustion of the composites containing silane treated CNCs promoted char formation and enhanced thermal stability. The composites containing (1:1) silane treated CNCs exhibited the better crystallization ability, highest storage modulus, and lowest tan δ value compared to the other silane treated systems indicating improved dispersion of CNC. The polysiloxane network provided an efficient surface covering of the CNC molecules, imparting reduced polar surface characteristics and enhancing the overall mechanical properties of the composites. [ABSTRACT FROM AUTHOR]

Synthetic polymers are ubiquitous materials widely used in construction, automotive, electronics, and countless commercial products. With the growing trend of polymer applications in everyday life, upholding the rigorous fire safety regulations has become a matter of concern. In this regard, numerous studies have been conducted for improving the fire retardancy of polymers, mainly through incorporating a diverse group of fire‐retardant compounds into polymer‐based composites. This review article aims to present a comprehensive overview of recent advances in the fire‐retardant categories for polymeric materials especially emphasizing the nanosized fire retardants. Along with an attempt to focus attention on the consumption of conventional and possibly harmful fire retardants, potential eco‐friendly alternatives are represented. A detailed discussion on the flame retardation mechanisms and conventional fire characterization techniques are also discussed. [ABSTRACT FROM AUTHOR]

Global energy consumption is expected to grow by 56% between 2010 and 2040. Renewable energy is one of the fastest-growing energy resources, and biomass is a major feedstock for providing renewable energy. It constitutes up to 35% of the main energy consumption in developing countries. Densified solid biofuel with high density gets a lot of attention due to its uniform shape and low heating cost. When considering densified solid biofuels as a viable solution for energy production, its quality needs to be improved. Solid biofuel quality is a function of the chemical composition and physical properties of the raw materials. It is widely reported that the raw material chemical composition has a major effect on the final solid biofuel quality, as it influences the heating value, ash content, and mechanical durability. The moisture content influences the net heating value, combustion efficiency, and mechanical durability of solid biofuels. The bulk density influences the mechanical durability, thermal characteristics, as well as handling and storage costs of solid biofuels. This work reviewed the latest developments on the effects of the chemical composition, moisture content, and bulk density of raw materials on the thermal efficiency, emission, and mechanical durability of densified solid biofuels. [ABSTRACT FROM AUTHOR]

Highlights • Biochar, a carbon rich material is porous and thermally stable. • Addition of biochar improves the physico-mechanical properties of composites. • Coupling agent is more effective in HDPE-wood fiber matrix than biochar. • Biochar improves the thermal stability and reduces water absorption of composites. Abstract Bio-composite samples were manufactured using poly (lactic acid) (PLA), high density polyethylene (HDPE), biochar, wood flour, and coupling agent. Biochar, a carbon rich and thermally stable material, derived from switchgrass under controlled pyrolysis was tested as a functional filler. The study aimed at investigating the impact of biochar and wood fiber in the presence of coupling agent (maleic anhydride) on the properties of bio-composites. The bio-composite physical, mechanical and thermal properties were characterized using microscopy, dynamic mechanical analysis (DMA), thermogravimetric analysis (TGA), Fourier transform-infrared spectroscopy (FT-IR). The results showed that coupling agent is more compatible with wood flour than biochar. Addition of biochar reduced the moisture absorption and linear thermal expansion of filled bio-composites. It also improved the composites strength and moduli, showing a reinforcing nature of biochar. The TGA thermograms confirmed the improved stability of composites with biochar. Coupling agent was more effective in HDPE matrix reinforced by wood flour than biochar. Overall, this study demonstrated that biochar can be a good filler for improving dimensional stability, mechanical properties, and thermal stability of bio-composites. [ABSTRACT FROM AUTHOR]

ABSTRACT: Cellulose nanocrystal (CNCs)‐reinforced poly(lactic acid) (PLA) nanocomposites were prepared using twin screw extrusion followed by injection molding. Masterbatch approach was used to achieve more efficient dispersion of CNCs in PLA matrix. Modified CNCs (b‐CNCs) were prepared using benzoic acid as a nontoxic material through a green esterification method in a solvent‐free technique. Transmission electron microscopy images did not exhibit significant differences in the structure of b‐CNCs as compared with unmodified CNCs. However, a reduction of 6.6–15.5% in the aspect ratio of b‐CNCs was observed. The fracture surface of PLA‐b‐CNCs nanocomposites exhibited rough and irregular pattern which confirmed the need of more energy for fracture. Pristine CNCs showed a decrease in the thermal stability of nanocomposites, however, b‐CNCs nanocomposites exhibited higher thermal stability than pure PLA. The average storage modulus was improved by 38 and 48% by addition of CNCs and b‐CNCs in PLA, respectively. The incorporation of b‐CNCs increased Young's modulus, ultimate tensile stress, elongation at break, and impact strength by 27.02, 10.90, 4.20, and 32.77%, respectively, however, CNCs nanocomposites exhibited a slight decrease in ultimate strength and elongation at break. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018, 135, 46468. [ABSTRACT FROM AUTHOR]

Biopolymers are an emerging class of materials being widely pursued due to their ability to degrade in short periods of time. Understanding and evaluating the recyclability of biopolymers is paramount for their sustainable and efficient use in a cost-effective manner. Recycling has proven to be an important solution, to control environmental and waste management issues. This paper presents the first recycling assessment of Solanyl, Bioflex, polylactic acid (PLA) and PHBV using a melt extrusion process. All biopolymers were subjected to five reprocessing cycles. The thermal and mechanical properties of the biopolymers were investigated by GPC, TGA, DSC, mechanical test, and DMA. The molecular weights of Bioflex and Solanyl showed no susceptible effect of the recycling process, however, a significant reduction was observed in the molecular weight of PLA and PHBV. The inherent thermo-mechanical degradation in PHBV and PLA resulted in 20% and 7% reduction in storage modulus, respectively while minimal reduction was observed in the storage modulus of Bioflex and Solanyl. As expected from the Florry-Fox equation, recycled PLA with a high reduction in molecular weight (78%) experienced 9% reduction in glass transition temperature. Bioflex and Solanyl showed 5% and 2% reduction in molecular weight and experienced only 2% reduction in glass transition temperature. These findings highlight the recyclability potential of Bioflex and Solanyl over PLA and PHBV. [ABSTRACT FROM AUTHOR]