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Given the global challenge of plastic pollution, the development of new bioplastics to replace conventional polymers has become a priority. It is therefore essential to achieve a balance in the performances of biopolymers in order to improve their commercial availability. In this topic, this study aims to investigate the morphology and properties of poly(lactic acid) (PLA)/ poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) (PHBHHx) (at a ratio of 75/25 (w/w)) blends reinforced with halloysite nanotubes (HNTs) and compatibilized with poly(lactic acid)-grafted maleic anhydride (PLA-g-MA). HNTs and PLA-g-MA were added to the polymer blend at 5 and 10 wt.%, respectively, and everything was processed via melt compounding. A scanning electron microscopy (SEM) analysis shows that HNTs are preferentially localized in PHBHHx nodules rather than in the PLA matrix due to its higher wettability. When HNTs are combined with PLA-g-MA, a finer and a more homogeneous morphology is observed, resulting in a reduction in the size of PHBHHx nodules. The presence of HNTs in the polymer blend improves the impact strength from 12.7 to 20.9 kJ/mm2. Further, with the addition of PLA-g-MA to PLA/PHBHHX/HNT nanocomposites, the tensile strength, elongation at break, and impact strength all improve significantly, rising from roughly 42 MPa, 14.5%, and 20.9 kJ/mm2 to nearly 46 MPa, 18.2%, and 31.2 kJ/mm2, respectively. This is consistent with the data obtained via dynamic mechanical analysis (DMA). The thermal stability of the compatibilized blend reinforced with HNTs is also improved compared to the non-compatibilized one. Overall, this study highlights the effectiveness of combining HNTs and PLA-g-AM for the properties enhancement of PLA/PHBHHx blends. [ABSTRACT FROM AUTHOR]

Biocompostable composites based of ethylene‐co‐vinyl acetate (EVA) copolymer were prepared by using a twin‐screw extruder. The compatibility between EVA/starch composites were improved either by addition of polyethylene‐grafted maleic anhydride (PE‐g‐MA), or by reactive extrusion with maleic anhydride (MA) and benzoyl peroxide. The crystallinity of the non‐compatibilized composites increased with the starch content. The addition of PE‐g‐MA increased the crystallinity of the composites made with up to 20 wt% of starch. The thermal stability of EVA/starch composites decreased with increasing the starch content, and the addition of PE‐g‐MA compatibilizer enhanced the thermal stability of the composite. The in‐situ grafting with MA and PBO led to an increase in the thermal stability of the composites containing higher amounts of starch. Further, the mechanical properties of the compatibilized EVA/starch composites were improved with increasing the starch content and this was ascribed to the improved interfacial interactions between starch and EVA. POLYM. COMPOS., 40:3242–3253, 2019. © 2019 Society of Plastics Engineers [ABSTRACT FROM AUTHOR]

The paper provides some experimental data on the effects of a poly(3-hydroxybutyrate-co-3-hydroxyvalerate) grafted maleic anhydride (PHBV-g-MA) used as the compatibilizer for poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV)/olive husk flour (OHF) composites prepared by melt compounding. The natural filler was added to PHBV at various contents, i.e. 10, 20, and 30 wt%, while the amount of PHBV-g-MA was 5 wt% based on neat PHBV. Morphology, contact angle measurements, water absorption (WA), mechanical, viscoelastic, and barrier properties of the various composites were investigated with and without the compatibilizer. The study showed through scanning electron microscopy that the addition of PHBV-g-MA to PHBV/OHF composites resulted in better and finer dispersion of the filler in the matrix, even at a higher content ratio, indicating improved affinity between the components. This is in agreement with the decrease in both surface energy and WA. Furthermore, tensile and dynamic mechanical measurements indicated a reinforcing effect of OHF in PHBV composites, being more pronounced in the presence of PHBV-g-MA. The barrier properties against oxygen and water vapor were also improved for the compatibilized composites. [ABSTRACT FROM AUTHOR]

ABSTRACT The degradation of uncompatibilized and compatibilized PP/PA-6 (70/30 wt %) with PP- g-MA under accelerated UV light was investigated using Fourier Transform Infrared Spectroscopy (FTIR) spectroscopy, melt flow index (MFI) tester, tensile test, differential scanning calorimetry (DSC), thermogravimetric analysis (TGA) and scanning electron microscopy (SEM). FTIR analysis of the structure of the compatibilized and uncompatibilized blends after exposure to UV light showed the formation of photoproducts corresponding to both components. The MFI and mechanical results obtained revealed that photooxidation started primarily in PA-6 rather than PP. In addition, the uncompatibilized blends exhibited a higher degradation rate compared to neat polymers for long exposure time, and the addition of PP- g-MA increased slightly their ageing rate in accordance with TGA data. Further, DSC analysis showed an increase in the crystallinity index and a decrease in the melting temperature of PP and PA-6 after UV exposure either as neat polymers or as blend components. SEM micrographs of the cryo-fractured surfaces of the samples illustrated the formation of cracks and fractures after UV irradiation. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015, 132, 41722. [ABSTRACT FROM AUTHOR]

Blends of poly(3-hydroxybutyrate- co-3-hydroxyvalerate) (PHBV) and polylactide (PLA) with different PHBV/PLA weight ratios (100/0, 75/25, 50/50, 25/75, 0/100) were prepared by melt compounding. To improve the miscibility between the two components of the blend, low amount of compatibilizing agent (5 wt%), obtained by grafting maleic anhydride onto PHBV, was used. When compared with the uncompatibilized blends, the compatibilizer presence induces a greater interfacial adhesion. The effect of Cloisite 30B (C30B) on the blend morphology and the blend properties was also investigated. The morphology of the different blends as well as the evolution of their material properties were discussed in terms of the nanoclay and compatibilizing agent contents. A synergistic effect of compatibilizer and C30B was highlighted leading to an improved miscibility of the two blend components. The resulting properties were correlated with the morphology observed for the different blends. POLYM. ENG. SCI., 54:2239-2251, 2014. © 2013 Society of Plastics Engineers [ABSTRACT FROM AUTHOR]

This work aims to study the effects of date stone flour (DSF) on morphology, thermal, and mechanical properties of polypropylene (PP) composites in the absence and presence of ethylene-butyl acrylate-glycidyl methacrylate (EBAGMA) used as the compatibilizer. DSF was added to the PP matrix at loading rates of 10, 20, 30, and 40 wt %, while the amount of compatibilizer was fixed to the half of the filler content. The study showed through scanning electron microscopy analysis that EBAGMA compatibilizer improved the dispersion and the wettability of DSF in the PP matrix. Thermogravimetric analysis (TGA) indicated a slight decrease in the decomposition temperature at onset ( Tonset) for all composite materials compared to PP matrix, whereas the thermal degradation rate was slower. Differential scanning calorimetry (DSC) data revealed that the melting temperature of PP in the composite materials remained almost unchanged. The nucleating effect of DSF was however reduced by the compatibilizer. Furthermore, the incorporation of DSF resulted in the increase of stiffness of the PP composites accompanied by a significant decrease in both the stress and strain at break. The addition of EBAGMA to PP/DSF composites improved significantly the ductility due to the elastomeric effect of EBAGMA. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013 [ABSTRACT FROM AUTHOR]

The paper reports some results of an experimental study on ethylene vinyl acetate (EVA) copolymer/olive husk flour (OHF) composites incorporated at various filler ratios (15, 30 and 45 wt%) in the absence and the presence of ethylene-butyl acrylate-glycidyl methacrylate (EBAGMA) terpolymer used as a compatibilizer. The composite samples have been prepared by melt blending and their chemical structure, as well as morphological, mechanical and water absorption properties investigated. It is shown that the compatibility of EVA/OHF composites is improved by the addition of EBAGMA terpolymer. Indeed, FT-IR analysis shows that chemical interactions have occurred between the compatibilizer and the base blend components. Morphological results from SEM shows better dispersion of the wood particles in the EVA matrix and the resulting composite samples exhibit better tensile properties at break and lower water absorption than the uncompatibilized ones. Moreover, the results indicate that the loading concentrations of both OHF and EBAGMA have an effect on the composite properties. [ABSTRACT FROM AUTHOR]

Blends of poly (3-hydroxybutyrate- co -3-hydroxyvalerate) (PHBV) and poly (butylene succinate) (PBS) (50:50 w/w) were prepared by melt mixing. 5 wt% of compatibilizing agent, obtained by grafting of maleic anhydride onto PHBV, was used to improve the miscibility between the blend components. The influence of the presence of both sepiolite and compatibilizer was studied by evaluating the effect of repeated extrusion cycles (up to 6) on the morphology and the functional properties of materials. Changes in thermal, morphological, rheological and mechanical properties were investigated. All the results showed that PHBV is the more sensitive component towards recycling due to thermomechanical degradation, but PBS as well as sepiolite and compatibilizer play a stabilizing role on PHBV due to improved morphology. The mechanical characteristics measured at different scales remain more or less constant compared to the initial ones revealing the preservation of the mechanical properties of the different samples after reprocessing. This paper highlights a synergistic effect induced by the presence of both compatibilizer and sepiolite leading to an improved recyclability of the resulting materials compared to neat polymers. [ABSTRACT FROM AUTHOR]

Blends of poly(3-hydroxybutyrate- co -3-hydroxyvalerate) (PHBV) and poly(butylene succinate) (PBS) with different PHBV/PBS weight ratios (100/0, 75/25, 50/50 and 0/100) were elaborated by melt mixing. The morphological investigation of the different samples, in comparison with that of neat PHBV and neat PBS, pointed out that PHBV/PBS blends form a biphasic system over the whole composition range. Low amount of compatibilizing agent (5 wt%), obtained by grafting maleic anhydride (MA) onto PHBV, i.e. PHBV-g-MA, was used for improving the miscibility between the two components of the blend. The incorporation of a fibrous filler as the sepiolite, easily dispersible in a polymer matrix, was also investigated. The morphology of the different blends as well as the evolution of their material properties were discussed in terms of the sepiolite and compatibilizing agent contents. The dispersion of PBS in the PHBV matrix markedly became finer with incorporation of sepiolite and PHBV-g-MA, due to enhanced interactions between the components. This paper highlighted a synergistic effect induced by the presence of both compatibilizer and sepiolite leading to an improved miscibility of the two blend components. The resulting properties were correlated with the morphology observed for the different blends. [ABSTRACT FROM AUTHOR]