Functionalization of Partially Bio-Based Poly(Ethylene Terephthalate) by Blending with Fully Bio-Based Poly(Amide) 10,10 and a Glycidyl Methacrylate-Based Compatibilizer
Abstract:This work shows the potential of binary blends composed of partially bio-based poly(ethyelene terephthalate) (bioPET) and fully bio-based poly(amide) 10,10 (bioPA1010). These blends are manufactured by extrusion and subsequent injection moulding and characterized in terms of mechanical, thermal and thermomechanical properties. To overcome or minimize the immiscibility, a glycidyl methacrylate copolymer, namely poly(styrene-ran-glycidyl methacrylate) (PS-GMA; Xibond™ 920) was used. The addition of 30 wt % bioPA… Show more
“…These additives are generally based on polymers with low molecular weight (Mw), oligomers, or even, more recently, functionalized vegetable oils with several reactive groups that are prone to form chemical bonds during melt processing [48,49]. In this sense, some commercially available copolymers and oligomers based on epoxy, maleic, or glycidyl methacrylate groups have successfully compatibilized biopolyesters and their green composites with lignocellulosic particles [22,[50][51][52]. The present study evaluated and compared the effect of surface treatments and different reactive compatibilizers on the performance of green composites based on PLA and short FFs prepared by twin-screw extrusion (TSE) and injection molding.…”
Section: Methodsmentioning
confidence: 99%
“…The three tested compatibilizers were added as different parts per hundred resin (phr) of composite. Particularly, PS-co-GMA and ESAO were both added at 1 phr, as this content has reported to enhance the interaction between biopolymers without leading undesired effects such as gel formation [50,59]. The selected MLO content was 5 phr since higher oil loadings could exert a negative effect by saturation [60].…”
Section: Reactive Extrusion Of the Green Compositesmentioning
confidence: 99%
“…Furthermore, in the case of the green composite samples processed with ESAO, PS-co-GMA and, even, MLO, this crystallinity restriction can be related to the formation of chain-extended and/or branched structures of PLA with a higher impairment to crystallize [74,89]. Some authors have additionally concluded that this reaction can create cross-linked structures that could lead to difficulties in the chains mobility and, hence, cold crystallization is delayed [50,74,90]. In the case of the PLA/FF + MLO piece, showing the highest T cc value, that is, 124.5 • C, the newly formed spherical-shape phases dispersed in the PLA matrix could further contribute to delay crystallization of PLA.…”
Section: Thermal Properties Of the Green Composite Piecesmentioning
Green composites made of polylactide (PLA) and short flaxseed fibers (FFs) at 20 wt % were successfully compounded by twin-screw extrusion (TSE) and subsequently shaped into pieces by injection molding. The linen waste derived FFs were subjected to an alkalization pretreatment to remove impurities, improve the fiber surface quality, and make the fibers more hydrophobic. The alkali-pretreated FFs successfully reinforced PLA, leading to green composite pieces with higher mechanical strength. However, the pieces also showed lower ductility and toughness and the lignocellulosic fibers easily detached during fracture due to the absence or low interfacial adhesion with the biopolyester matrix. Therefore, four different compatibilization strategies were carried out to enhance the fiber–matrix interfacial adhesion. These routes consisted on the silanization of the alkalized FFs with a glycidyl silane, namely (3-glycidyloxypropyl) trimethoxysilane (GPTMS), and the reactive extrusion (REX) with three compatibilizers, namely a multi-functional epoxy-based styrene-acrylic oligomer (ESAO), a random copolymer of poly(styrene-co-glycidyl methacrylate) (PS-co-GMA), and maleinized linseed oil (MLO). The results showed that all the here-tested compatibilizers improved mechanical strength, ductility, and toughness as well as the thermal stability and thermomechanical properties of the green composite pieces. The highest interfacial adhesion was observed in the green composite pieces containing the silanized fibers. Interestingly, PS-co-GMA and, more intensely, ESAO yielded the pieces with the highest mechanical performance due to the higher reactivity of these additives with both composite components and their chain-extension action, whereas MLO led to the most ductile pieces due to its secondary role as plasticizer for PLA.
“…These additives are generally based on polymers with low molecular weight (Mw), oligomers, or even, more recently, functionalized vegetable oils with several reactive groups that are prone to form chemical bonds during melt processing [48,49]. In this sense, some commercially available copolymers and oligomers based on epoxy, maleic, or glycidyl methacrylate groups have successfully compatibilized biopolyesters and their green composites with lignocellulosic particles [22,[50][51][52]. The present study evaluated and compared the effect of surface treatments and different reactive compatibilizers on the performance of green composites based on PLA and short FFs prepared by twin-screw extrusion (TSE) and injection molding.…”
Section: Methodsmentioning
confidence: 99%
“…The three tested compatibilizers were added as different parts per hundred resin (phr) of composite. Particularly, PS-co-GMA and ESAO were both added at 1 phr, as this content has reported to enhance the interaction between biopolymers without leading undesired effects such as gel formation [50,59]. The selected MLO content was 5 phr since higher oil loadings could exert a negative effect by saturation [60].…”
Section: Reactive Extrusion Of the Green Compositesmentioning
confidence: 99%
“…Furthermore, in the case of the green composite samples processed with ESAO, PS-co-GMA and, even, MLO, this crystallinity restriction can be related to the formation of chain-extended and/or branched structures of PLA with a higher impairment to crystallize [74,89]. Some authors have additionally concluded that this reaction can create cross-linked structures that could lead to difficulties in the chains mobility and, hence, cold crystallization is delayed [50,74,90]. In the case of the PLA/FF + MLO piece, showing the highest T cc value, that is, 124.5 • C, the newly formed spherical-shape phases dispersed in the PLA matrix could further contribute to delay crystallization of PLA.…”
Section: Thermal Properties Of the Green Composite Piecesmentioning
Green composites made of polylactide (PLA) and short flaxseed fibers (FFs) at 20 wt % were successfully compounded by twin-screw extrusion (TSE) and subsequently shaped into pieces by injection molding. The linen waste derived FFs were subjected to an alkalization pretreatment to remove impurities, improve the fiber surface quality, and make the fibers more hydrophobic. The alkali-pretreated FFs successfully reinforced PLA, leading to green composite pieces with higher mechanical strength. However, the pieces also showed lower ductility and toughness and the lignocellulosic fibers easily detached during fracture due to the absence or low interfacial adhesion with the biopolyester matrix. Therefore, four different compatibilization strategies were carried out to enhance the fiber–matrix interfacial adhesion. These routes consisted on the silanization of the alkalized FFs with a glycidyl silane, namely (3-glycidyloxypropyl) trimethoxysilane (GPTMS), and the reactive extrusion (REX) with three compatibilizers, namely a multi-functional epoxy-based styrene-acrylic oligomer (ESAO), a random copolymer of poly(styrene-co-glycidyl methacrylate) (PS-co-GMA), and maleinized linseed oil (MLO). The results showed that all the here-tested compatibilizers improved mechanical strength, ductility, and toughness as well as the thermal stability and thermomechanical properties of the green composite pieces. The highest interfacial adhesion was observed in the green composite pieces containing the silanized fibers. Interestingly, PS-co-GMA and, more intensely, ESAO yielded the pieces with the highest mechanical performance due to the higher reactivity of these additives with both composite components and their chain-extension action, whereas MLO led to the most ductile pieces due to its secondary role as plasticizer for PLA.
“…In contrast, biobased polymers with the same chemical structures as conventional polymers, such as bioPE, bioPP, and bioPET, also share the same mechanical and thermal behaviours. These biopolymers differ in the origin of the components out of which they are synthesised, as they come from renewable sources instead of oil [ 1 , 4 , 9 , 10 , 11 , 12 ].…”
In this study, binary blends of biodegradable polymers were prepared to improve the ductile properties of those that have a more rigid and/or brittle. Specifically, PLA, PHA and TPS were blended with different amounts of PBS with the objective of reducing the stiffness and brittleness of the three polymers. The compatibility of the blends and their resulting mechanical properties were studied. The flexibility of the blends increased with the addition of PBS; however, a limited compatibility was achieved, leading to a low impact resistance improvement. For this reason, other blend options with an EVA-based material were studied, increasing the impact resistance and flexibility of the PLA material in this case.
“…BioPE is a polymer that is synthesized from ethylene monomer derived from the dehydration of bioethanol obtained from the glucose of different biological raw materials such as sugar cane, sugar beet, corn or wheat starch, and lignocellulosic materials (Tsiropoulos et al, 2015). This material can reach up to 95% biobased content, which makes it more environmentally friendly than petroleum-based polyethylene (Jorda et al, 2019). Furthermore, CO 2 emissions from petrochemical PE are estimated to be 2.1 tonnes per tonne of polymer whereas for BioPE the emissions are -2.5 tonnes of CO 2 , indicating that it binds carbon, thus reducing CO 2 emissions to the atmosphere and the environmental impact compared to its petroleum-based counterpart (Garcia-Garcia, Carbonell-Verdu, Jordá-Vilaplana, Balart, & Garcia-Sanoguera, 2016;Samper-Madrigal, Fenollar, Dominici, Balart, & Kenny, 2015).…”
<p class="JARTEAbstract">In this study was analyzed the effect of three different compatibilizers polyethylene-graft-maleic anhydride (PE-g-MA), unmodified halloysite nanotubes (HNTs), and HNTs treated by silanization with (3-glycidyloxypropyl) trimethoxysilane (GLYMO) (silanized HNTs) in blends of bio-based high-density polyethylene (bioPE) and poly(butylene succinate) (PBS) with a weight ratio of (70/30). Each compatibilizer was added in a proportion of (3 phr regarding PBS). Standard samples were obtained by extrusion and subsequent injection molding. The analyzes of the samples were performed by mechanical tests, thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), dynamic mechanical thermal analysis (DMTA), field emission scanning electron microscopy (FESEM), and wettability (θ<sub>w</sub>). Results suggest that the addition of modified HNTs (silanized HNTs) allowed to obtain better properties than samples compatibilized with unmodified HNTs and PE-g-MA, due to it contributes with the improvement in mechanical properties regarding bioPE/PBS blend, for instance, the tensile modulus and elongation at break increase about 8% and 13%, respectively. In addition, it was determined through FESEM images and that silanized HNTs particles were better dispersed over the matrix, which in fact contribute to the enhance in mechanical properties. TGA showed that silanized HNTs delay the degradation temperature regarding the uncompatibilized blend. While DMTA indicated the reduction in the mobility of the chains in samples with unmodified and modified HNTs. Therefore, it was successfully obtained compatibilized bioPE/PBS blends, which constitutes an interesting option to develop new sustainable polymers.</p>
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