In this work, uncompatibilized and compatibilized blends of low density polyethylene (LDPE) and poly(lactic acid) (PLA) were subjected to several investigations: Fourier transform infrared (FTIR) spectroscopy, morphological analysis and mechanical testing (tensile, impact, microhardness). The copolymer (ethylene-coglycidyl methacrylate) (EGMA) was used as compatibilizer. The percentages of PLA in LDPE/PLA samples ranged from 0 to 100 wt% while the EGMA was added to the blend 60/40 (LDPE/PLA) at concentrations of 2, 5, 7, 10, 15 and 20 parts per hundred (phr). FTIR analysis showed the absence of any interaction between LDPE and PLA, but after addition of compatibilizer, reactions between epoxy groups of EGMA and carboxylic or hydroxyl groups of PLA were confirmed. Tensile and impact tests revealed a loss of ductility of LDPE with the incorporation of PLA, except for the composition 80/20 (LDPE/PLA). However, the addition of 15 phr of EGMA led to the maximum increase in the elongation-at-break (about three times the value of uncompatibilized blend) and in the impact strength, but a marginal improvement was observed for tensile strength. SEM micrographs confirmed that the enhancement of mechanical properties is due to the improvement of the interfacial adhesion between different phases owing to the presence of EGMA. The microhardness values of the different blends (uncompatibilized or compatibilized) were in good agreement with the macroscopic mechanical properties (tensile and impact strengths).
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Zinc oxide nanoparticles (ZnO NPs) are prepared by sol-gel process, using both polyethylene glycol (PEG-400) as surfactant and propyltrimethoxysilane (PTMS) as capping agent. Surface modification is performed in situ procedure. The physical parameters such as strain and stress values are calculated via the Williamson-Hall plot (W&H) assuming a uniform deformation model (UDM) and uniform stress deformation model, and by the size and strain plot method (SSP). The results show that the crystallite size estimated from Scherrer's formula, (W&H), (UDM), (SSP) and the particle size estimated from DSL are inter-correlated, which confirm the small size and the isotropic nature of our ZnO NPs. The FTIR spectroscopy illustrates that PEG-400 and PTMS could be adsorbed at the ZnO NPs surface. The distinct emission peak in the blue band is located at 490 nm and E 2 (high) mode is situated at 436 cm -1 . Both results confirm the oxygen deficiency in the ZnO NPs.
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