scholarly journals Nonisothermal Crystallization Kinetics of Polylactic Acid under the Influence of Polyolefin Elastomers

2020 ◽  
Vol 4 (2) ◽  
pp. 65
Author(s):  
Azadeh Khosravi ◽  
Abdolhossein Fereidoon ◽  
Mohammad Mehdi Khorasani ◽  
Vincent Berthe ◽  
Henri Vahabi ◽  
...  
Keyword(s):  
Crystallization Kinetics ◽  
Crystallization Kinetic ◽  
Ethylene Vinyl Acetate ◽  
Poly Lactic Acid ◽  
Experimental Investigations ◽  
Melt Mixing ◽  
Dsc Measurements ◽  
Theoretical Approaches ◽  
The Matrix ◽  
Kinetics Of

Crystallization kinetics of various blends of poly(lactic acid) (PLA)/polyolefin elastomer (POE) was studied through nonisothermal experimental investigations and theoretical approaches. The PLA/POE blends were prepared in a melt mixing process by using two types of POEs and compatibilizers. The rubber phases used were adopted on the basis of polyethylene (PE) and polypropylene (PP) type olefin elastomers. The effects of two kinds of compatibilizers containing ethylene vinyl acetate copolymer (EVA) and ethylene acrylic ester-glycidyl methacrylate terpolymer (EGMA) on the morphology and various parameters of crystallization of PLA were investigated using scanning electron microscopy (SEM) and differential scanning calorimeter (DSC) measurements, respectively. The morphology investigations on PLA blends containing PP based olefin elastomers showed that the introduction of EGMA compatibilizer into the matrix led to a more than 100% reduction in the size of the rubber droplets. The experimental measurements of crystallization behavior of various PLA/POE blends showed that the POEs and compatibilizers could cause a fall in the initial crystallization temperature more than 13 °C. The theoretical approaches used for studying the kinetics of crystallization of PLA in the presence of various POEs and compatibilizers indicated a decrease in the crystallinity of PLA and a 64% reduction in the activation energy compared to the neat PLA. The results suggest that the largest variation in the crystallization kinetic parameters of PLA was resulted from the PP based olefin elastomer and EGMA compatibilizer.

scholarly journals Poly(lactic Acid)–Biochar Biocomposites: Effect of Processing and Filler Content on Rheological, Thermal, and Mechanical Properties

Polymers ◽  
2020 ◽  
Vol 12 (4) ◽  
pp. 892 ◽  
Author(s):  
Rossella Arrigo ◽  
Mattia Bartoli ◽  
Giulio Malucelli
Keyword(s):  
Lactic Acid ◽  
Filler Content ◽  
Processing Method ◽  
Poly Lactic Acid ◽  
Rheological Characterization ◽  
Scanning Calorimetry ◽  
Melt Mixing ◽  
Dsc Measurements ◽  
The Matrix ◽  
Filler Dispersion

Biocomposites based on poly(lactic acid) (PLA) and biochar (BC) particles derived from spent ground coffee were prepared using two different processing routes, namely melt mixing and solvent casting. The formulated biocomposites were characterized through rheological, thermal, and mechanical analyses, aiming at evaluating the effects of the filler content and of the processing method on their final properties. The rheological characterization demonstrated the effectiveness of both exploited strategies in achieving a good level of filler dispersion within the matrix, notwithstanding the occurrence of a remarkable decrease of the PLA molar mass during the processing at high temperature. Nevertheless, significant alterations of the PLA rheological behavior were observed in the composites obtained by melt mixing. Differential scanning calorimetry (DSC) measurements indicated a remarkable influence of the processing method on the thermal behavior of biocomposites. More specifically, melt mixing caused the appearance of two melting peaks, though the structure of the materials remained almost amorphous; conversely, a significant increase of the crystalline phase content was observed for solvent cast biocomposites containing low amounts of filler that acted as nucleating agents. Finally, thermogravimetric analyses suggested a catalytic effect of BC particles on the degradation of PLA; its biocomposites showed decreased thermal stability as compared with the neat PLA matrix.

Glass Forming Ability and Crystallization Kinetics of Al-Mg-Ni-La Metallic Glasses

2014 ◽  
Vol 960-961 ◽  
pp. 161-164 ◽  
Author(s):  
Juan Mu ◽  
Hai Feng Zhang
Keyword(s):  
Crystallization Kinetics ◽  
Glass Forming Ability ◽  
Continuous Heating ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Glass Forming ◽  
Dsc Measurements ◽  
Mg Addition ◽  
Kinetics Of ◽  
Thermal Stability Of

Glass forming ability and crystallization kinetics of Al-Mg-Ni-La alloys have been investigated by X-ray diffraction (XRD) and differential scanning calorimetry (DSC). The maximum thickness achievable in glasses of Al76Mg11Ni8La5and Al69Mg18Ni8La5ribbons were 200 and 120 μm, respectively. The crystallization temperature and peak temperature indicated by DSC measurements displayed dependence on the heating rate during continuous heating, and were coincident with Lanoka’s relationship. The activation energies for the crystallization reactionExwere obtained from the Kissinger’s equation. The results show the Mg addition is beneficial to the thermal stability of the amorphous phase.

Nucleation and crystallization kinetics of poly(lactic acid)

2011 ◽  
Vol 522 (1-2) ◽  
pp. 128-134 ◽  
Author(s):  
Felice De Santis ◽  
Roberto Pantani ◽  
Giuseppe Titomanlio
Keyword(s):  
Lactic Acid ◽  
Crystallization Kinetics ◽  
Poly Lactic Acid ◽  
Kinetics Of

scholarly journals Crystallization Kinetics of Poly(lactic acid)–Graphene Nanoscroll Nanocomposites: Role of Tubular, Planar, and Scrolled Carbon Nanoparticles

2021 ◽  
Vol 7 (4) ◽  
pp. 75
Author(s):  
Oluwakemi Ajala ◽  
Caroline Werther ◽  
Rauf Mahmudzade ◽  
Peyman Nikaeen ◽  
Dilip Depan
Keyword(s):  
Mechanical Properties ◽  
Lactic Acid ◽  
Crystallization Kinetics ◽  
Crystallization Rate ◽  
Melting Behavior ◽  
Degree Of Crystallinity ◽  
Poly Lactic Acid ◽  
Avrami Model ◽  
Superior Mechanical Properties ◽  
Kinetics Of

Graphene nanoscrolls (GNS) are 1D carbon-based nanoparticles. In this study, they were investigated as a heterogeneous nucleating agent in the poly(lactic acid) (PLA) matrix. The isothermal and non-isothermal melting behavior and crystallization kinetics of PLA-GNS nanocomposites were investigated using a differential scanning calorimeter (DSC). Low GNS content not only accelerated the crystallization rate, but also the degree of crystallinity of PLA. The Avrami model was used to fit raw experimental data, and to evaluate the crystallization kinetics for both isothermal and non-isothermal runs through the nucleation and growth rate. Additionally, the effect of the dimensionality and structure of the nanoparticle on the crystallization behavior and kinetics of PLA is discussed. GNS, having a similar fundamental unit as CNT and GNP, were observed to possess superior mechanical properties when analyzed by the nanoindentation technique. The scrolled architecture of GNS facilitated a better interface and increased energy absorption with PLA compared to CNTs and GNPs, resulting in superior mechanical properties.

scholarly journals Barrier Properties and Hydrophobicity of Biodegradable Poly(lactic acid) Composites Reinforced with Recycled Chinese Spirits Distiller’s Grains

Polymers ◽  
2021 ◽  
Vol 13 (17) ◽  
pp. 2861
Author(s):  
Zhi-Jun Chen ◽  
Chi-Hui Tsou ◽  
Meng-Lin Tsai ◽  
Jipeng Guo ◽  
Manuel Reyes De Guzman ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Lactic Acid ◽  
Barrier Properties ◽  
Poly Lactic Acid ◽  
Control Group ◽  
Scanning Calorimetry ◽  
Melt Mixing ◽  
Distiller's Grains ◽  
The Matrix ◽  
Section Structure

Adding natural biomass to poly(lactic acid) (PLA) as a reinforcing filler is a way to change the properties of PLA. This paper is about preparing PLA/biomass composites by physically melting and blending Chinese Spirits distiller’s grains (CSDG) biomass and PLA to optimize the composite performance. Composites of modified PLA (MPLA) with varying amounts of CSDG were also prepared by the melt-mixing method, and unmodified PLA/CSDG composites were used as a control group for comparative analysis. The functional groups of MPLA enhanced the compatibility between the polymer substrate and CSDG. The composite water vapor/oxygen barrier and mechanical properties were studied. It was found that the barrier and mechanical properties of MPLA/CSDG composites were significantly improved. SEM was adopted to examine the tensile section structure of the composites, and the compatibility between the filler and the matrix was analyzed. An appropriate amount of CSDG had a better dispersibility in the matrix, and it further improved the interfacial bonding force, which in turn improved the composite mechanical properties. X-ray diffraction, thermogravimetric analysis, and differential scanning calorimetry were conducted to determine the crystalline properties and to analyze the stability of the composites. It was found that the CSDG content had a significant effect on the crystallinity. Barrier and biodegradation mechanisms were also discussed.

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