Method for Simultaneously Improving the Thermal Stability and Mechanical Properties of Poly(lactic acid): Effect of High-Energy Electrons on the Morphological, Mechanical, and Thermal Properties of PLA/MMT Nanocomposites

Langmuir ◽  
2012 ◽  
Vol 28 (34) ◽  
pp. 12601-12608 ◽  
Author(s):  
De-Yi Wang ◽  
Uwe Gohs ◽  
Nian-Jun Kang ◽  
Andreas Leuteritz ◽  
Regine Boldt ◽  
...  
2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Chaitra Venkatesh ◽  
Yuanyuan Chen ◽  
Zhi Cao ◽  
Shane Brennan ◽  
Ian Major ◽  
...  

Abstract Poly (lactic acid)/halloysite nanotube (PLA/HNT) nanocomposites have been studied extensively over the past few years owing to the interesting properties of the polymer, PLA, and the nanoclay, HNT, individually and as composites. In this paper, the influence of the screw speed during extrusion was investigated and was found to have a significant impact on the mechanical and thermal performance of the extruded PLA/HNT nanocomposites. To determine the effect of screw speed on PLA/HNT nanocomposites, 5 and 10 wt% of HNTs were blended into the PLA matrix through compounding at screw speeds of 40, 80, and 140 rpm. Virgin PLA was compounded for comparison. The resultant polymer melt was quench cooled onto a calendar system to produce composite films which were assessed for mechanical, thermal, chemical, and surface properties. Results illustrate that in comparison to 40 and 80 rpm, the virgin PLA when compounded at 140 rpm, indicated a significant increase in the mechanical properties. The PLA/HNT 5 wt% nanocomposite compounded at 140 rpm showed significant improvement in the dispersion of HNTs in the PLA matrix which in turn enhanced the mechanical and thermal properties. This can be attributed to the increased melt shear at higher screw speeds.


Materials ◽  
2018 ◽  
Vol 11 (10) ◽  
pp. 1893 ◽  
Author(s):  
Přemysl Menčík ◽  
Radek Přikryl ◽  
Ivana Stehnová ◽  
Veronika Melčová ◽  
Soňa Kontárová ◽  
...  

This paper explores the influence of selected commercial plasticizers structure, which are based on esters of citric acid, on mechanical and thermal properties of Poly(3-hydroxybutyrate)/Poly(lactic acid)/Plasticizer biodegradable blends. These plasticizers were first tested with respect to their miscibility with Poly(3-hydroxybutyrate)/Poly(lactic acid) (PHB/PLA) blends using a kneading machine. PHB/PLA/plasticizer blends in the weight ratio (wt %) of 60/25/15 were then prepared by single screw and corotating meshing twin screw extruders in the form of filament for further three-dimensional (3D) printing. Mechanical, thermal properties, and shape stability (warping effect) of 3D printed products can be improved just by the addition of appropriate plasticizer to polymeric blend. The goal was to create new types of eco-friendly PHB/PLA/plasticizers blends and to highly improve the poor mechanical properties of neat PHB/PLA blends (with majority of PHB) by adding appropriate plasticizer. Mechanical properties of plasticized blends were then determined by the tensile test of 3D printed test samples (dogbones), as well as filaments. Measured elongation at break rapidly enhanced from 21% for neat non-plasticized PHB/PLA blends (reference) to 328% for best plasticized blends in the form of filament, and from 5% (reference) to 187% for plasticized blends in the form of printed dogbones. The plasticizing effect on blends was confirmed by Modulated Differential Scanning Calorimetry. The study of morphology was performed by the Scanning Electron Microscopy. Significant problem of plasticized blends used to be also plasticizer migration, therefore the diffusion of plasticizers from the blends after 15 days of exposition to 110 °C in the drying oven was investigated as their measured weight loss. Almost all of the used plasticizers showed meaningful positive softening effects, but the diffusion of plasticizers at 110 °C exposition was quite extensive. The determination of the degree of disintegration of selected plasticized blend when exposed to a laboratory-scale composting environment was executed to roughly check the “biodegradability”.


2019 ◽  
Vol 972 ◽  
pp. 172-177
Author(s):  
Sirirat Wacharawichanant ◽  
Patteera Opasakornwong ◽  
Ratchadakorn Poohoi ◽  
Manop Phankokkruad

This work studied the effects of various types of cellulose fibers on the morphology, mechanical and thermal properties of poly(lactic acid) (PLA)/propylene-ethylene copolymer (PEC) (90/10 w/w) blends. The PLA/PEC blends before and after adding cellulose fibers were prepared by melt blending method in the internal mixer and molded by compression method. The morphological analysis observed that the presence of cellulose in PLA did not change the phase morphology of PLA, and PLA/cellulose composite surfaces were observed the cellulose fibers inserted in PLA matrix and fiber pull-out. The phase morphology of PLA/PEC blends was changed from brittle fracture to ductile fracture behavior and showed the phase separation between PLA and PEC phases. The presence of celluloses did not improve the compatibility between PLA and PEC phases. The tensile stress and strain curves found that the tensile stress of PLA was the highest value. The addition of all celluloses increased Young’s modulus of PLA. The PEC presence increased the tensile strain of PLA over two times when compared with neat PLA and PLA was toughened by PEC. The incorporation of cellulose fibers in PLA/PEC blends could improve Young’s modulus, tensile strength, and stress at break of the blends. The thermal stability showed that the degradation temperatures of all types of cellulose were less than the degradation temperatures of PLA. Thus, the incorporation of cellulose in PLA could not enhance the thermal stability of PLA composites and PLA/PEC composites. The degradation temperature of PEC was the highest value, but it could not improve the thermal stability of PLA. The incorporation of cellulose fibers had no effect on the melting temperature of the PLA blend and composites.


2013 ◽  
Vol 1499 ◽  
Author(s):  
Eda Acik ◽  
Ulku Yilmazer

ABSTRACTTernary nanocomposites of poly (lactic acid) (PLA) were produced by melt blending with two types of elastomers and five types of organoclays to obtain improved mechanical properties such as tensile strength, modulus and impact strength. One of the elastomers is a random copolymer of ethylene and glycidyl methacrylate (E-GMA) and the other one is a random terpolymer of ethylene-butyl acrylate-maleic anhydride (E-BA-MAH). Organically modified montmorillonites (OMMT) were utilized as nanofillers. XRD, DSC, tensile and impact tests were done on the injection molded samples. FTIR, SEM and TEM analyses are still in progress. As preliminary results, thermal analysis showed that the addition of compatibilizers and organoclays does not have a distinct effect on the thermal properties of the composites, and no evidence of nucleation activity of compatibilizers or organoclays was found. For all types of organoclays, the nanocomposites produced with E-GMA exhibited better mechanical properties in comparison to nanocomposites containing E-BA-MAH, especially for the impact strength.


2015 ◽  
Vol 37 ◽  
pp. 15 ◽  
Author(s):  
Azin Paydayesh ◽  
Ahmad Aref Azar ◽  
Azam Jalali Arani

In this work, Poly Lactic Acid/Poly methyl Methacrylate (PLA/PMMA) blends in various compositions prepared and morphology and properties of these blends was investigated. Moreover, the effect of adding different amounts of Graphene Nanoplatelets (GNP) on the morphology of the blends (by SEM), the interaction of nanopalates with polymer phases (by FTIR) and its effect on the mechanical properties and thermal stability of the samples were examined. The results of the study showed that in different amounts of graphene, these plates were preferentially located in the polymer phases dissimilarly and thus, caused the change of the blend morphology. In addition, measuring the mechanical properties by tensile test and results of thermal analysis by TGA indicated the improvement of thermal stability, modulus and mechanical strength and reduction of the elongation at break of graphene containing blends with increasing the loading of GNP. The changing behavior of the mechanical and thermal properties was proportional to the Graphene localization in blend phases.


Materials ◽  
2020 ◽  
Vol 13 (21) ◽  
pp. 4736 ◽  
Author(s):  
Soňa Kontárová ◽  
Radek Přikryl ◽  
Veronika Melčová ◽  
Přemysl Menčík ◽  
Matyáš Horálek ◽  
...  

This paper investigates the effect of plasticizer structure on especially the printability and mechanical and thermal properties of poly(3-hydroxybutyrate)-poly(lactic acid)-plasticizer biodegradable blends. Three plasticizers, acetyl tris(2-ethylhexyl) citrate, tris(2-ethylhexyl) citrate, and poly(ethylene glycol)bis(2-ethylhexanoate), were first checked whether they were miscible with poly(3-hydroxybutyrate)-poly(lactic acid) (PHB-PLA) blends using a kneading machine. PHB-PLA-plasticizer blends of 60-25-15 (wt.%) were then prepared using a corotating meshing twin-screw extruder, and a single screw extruder was used for filament preparation for further three-dimensional (3D) fused deposition modeling (FDM) printing. These innovative eco-friendly PHB-PLA-plasticizer blends were created with a majority of PHB, and therefore, poor mechanical properties and thermal properties of neat PHB-PLA blends were improved by adding appropriate plasticizer. The plasticizer also influences the printability of blends, which was investigated, based on our new specific printability tests developed for the optimization of printing conditions (especially printing temperature). Three-dimensional printed test samples were used for heat deflection temperature measurements and Charpy and tensile-impact tests. Plasticizer migration was also investigated. The macrostructure of 3D printed samples was observed using an optical microscope to check the printing quality and printing conditions. Tensile tests of 3D printed samples (dogbones), as well as extruded filaments, showed that measured elongation at break raised, from 21% for non-plasticized PHB-PLA reference blends to 84% for some plasticized blends in the form of filaments and from 10% (reference) to 32% for plasticized blends in the form of printed dogbones. Measurements of thermal properties (using modulated differential scanning calorimetry and oscillation rheometry) also confirmed the plasticizing effect on blends. The thermal and mechanical properties of PHB-PLA blends were improved by the addition of appropriate plasticizer. In contrast, the printability of the PHB-PLA reference seems to be slightly better than the printability of the plasticized blends.


2013 ◽  
Vol 844 ◽  
pp. 65-68
Author(s):  
Pranee Nuinu ◽  
Kittikorn Samosorn ◽  
Kittisak Srilatong ◽  
Siripa Tongbut ◽  
Sayant Saengsuwan

The aim of this research was to reduce and improve the brittleness and thermal properties of poly lactic acid (PLA), respectively. Epoxidized natural rubber (ENR) was used to enhance the toughness and rutile titanium dioxide (R-TiO2) as filler was also incorporated to improve the thermal properties of the PLA. 10wt% ENR with epoxidation contents of 25 mol% (ENR25) and 50 mol% (ENR50) and various R-TiO2contents (0-10 phr)were compounded with PLA by using a twin-screw extruder at 155-165°C and a rotor speed of 40 rpm. The pellets of blends were then formed a thin film using a cast film extruder machine and cooled down under air flow. Thermal and mechanical properties and morphology of PLA/ENR/R-TiO2thin film were investigated. The crystallinity of PLA was found to increase with addition of ENR. The mechanical properties of thin film showed that the ENR50 enhanced the elongation but reduced the tensile strength of PLA with addition of R-TiO2at 5 and 10 phr, respectively. The TGA indicated that the addition of 10 phr R-TiO2increased in the decomposition temperature at 5% weight loss (Td5%) of PLA/ENR film. Thus the thermal stability of PLA/ENR50 was found to improve with addition of R-TiO2. From morphology study, the ENR50 phase showed a good dispersion in the PLA matrix. In conclusion, the addition of ENR and R-TiO2was found to enhance both toughness and thermal stability of PLA.


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