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In this study, almond shell waste (ASW) as filling material, pure (ER), and waste polystyrene modified bisphenol-A type epoxy resin (ER-PS) were used to obtain biobased composite materials. The modification of ASW was carried out with NaOH and linoleic acid (LnA). Fourier transform infrared spectroscopy (FT-IR), Scanning electron microscopy (SEM), thermogravimetric analysis (TGA), and Particle size distribution analyses were used in the characterization of ASW. Composites were prepared at filling ratios of 10-20-30-40-50% by mass using the casting technique. The morphology of the composites was characterized by SEM. The effects of epoxy matrix type and BK filling ratio on composites' mechanical, thermal, and water sorption properties were investigated. Tensile strength and modulus of elasticity (e-modulus) values of ERPS/ASW composites were lower, and tensile elongation values were higher than ER/ASW composites. The highest tensile strength values of 95-129 MPa were obtained for LnA modified ASW composites. The order of the tensile strength of the prepared ER matrix composites according to the filler type is: linoleic acid-modified ASW (LnA-ASW)>NaOH treated ASW (NaOH-ASW) > unmodified ASW. The most suitable ASW ratio was found as 30% by mass. e-modulus values of all modified ASW composites were higher than the epoxy matrix. According to the hardness test results, there was no significant difference between the composites. The water sorption of the composites increased depending on the ASW ratio and had a weakening effect on the mechanical properties. [ABSTRACT FROM AUTHOR]

Polyethylene terephthalate (PET) waste has become a major challenge for the conservation of the environment due to difficult degradation. For this reason, it is important to develop new recycling strategies for reusing this waste. In this work, the electrospinning technique was used to synthesize composite nanofibers of polyvinylpyrrolidone (PVP), recycling PET (RPET) that was obtained from the chemical recycling of postconsumer PET with glycolysis and styrene (ST) as a crosslinking agent. The polymer solutions were analyzed by viscosity and frequency sweeping, while the composite nanofibers were characterized by scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis/differential scanning calorimetry (TGA/DSC), and nanoindentation to compare their properties. The PVP nanofibers presented an average diameter of 257 nm; the RPET/PVP and RPET/PVP/ST composite nanofibers had average diameters of 361 nm and 394 nm, respectively; and the modulus of elasticity and hardness of the RPET/PVP/ST composite nanofibers were 29 and 20 times larger, respectively, than those of the PVP nanofibers. With the synthesis of these composite nanofibers, a new approach to PET recycling is presented. [ABSTRACT FROM AUTHOR]

This study evaluates the effect of 1% to 5% NaOH treatments of cotton stalk particles on the chemical composition and physical and mechanical properties of particleboards produced with this material. Gas chromatography and Fourier transform infrared (FTIR) spectroscopy indicated that the extractive, hemicellulose, and lignin content of the particles decreased during the alkali treatments, whereas the cellulose content increased. Thermogravimetric analysis (TGA) indicated that the untreated particles exhibited higher thermal stability than the particles treated with NaOH. The decrease in thermal stability of alkali-treated particles seems to be due to degradation of chemical components. Alkali treatments raised water absorption (WA) and thickness swelling (TS) of the produced particleboards. Except for 1% NaOH, the treatments reduced the modulus of elasticity (MOE), modulus of rupture (MOR), and internal bond (IB) strength in relation to the board made with untreated particles. The 1% NaOH treatment of cotton stalks was more effective and beneficial, leading to particleboards with satisfying MOE, MOR, and IB values that met the requirements for general-purpose particleboards used in dry conditions, as indicated by the TS-EN 312 (2012) standard. [ABSTRACT FROM AUTHOR]