Readily Controllable Step-Growth Polymerization Method for Poly(lactic acid) Copolymers Having a High Glass Transition Temperature

2010 ◽  
Vol 11 (5) ◽  
pp. 1196-1201 ◽  
Author(s):  
Saara Inkinen ◽  
Mikael Stolt ◽  
Anders Södergård
2018 ◽  
Vol 1 (1) ◽  
pp. 526-535
Author(s):  
Benaniba Mohamed Tahar ◽  
Aouachria Kamira

Blends of poly(lactic acid) (PLA) and poly(ethylene glycol) (PEG) with various contents (0, 5, 10, 15, 20 and 30 weight %) and with different molecular weights (M¯w = 1000, 4000 and 6000 g/mol), called respectively PEG1, PEG2, and PEG3 were prepared by melt blending. Since glass transition temperature (Tg), T? and loss factor (tan ?) are relevant indicators of polymer chain mobility, plasticization has been studied by dynamic mechanical analysis (DMA) and differential scanning calorimetry (DSC). Low molecular weight (LMW) PEG enable increased miscibility with PLA and more efficient reduction of glass transition temperature (Tg) for concentrations of PEG less than 20%. This effect is not only enhanced by the LMW but also by increasing its content up to 20%. As expected, both T? and Tg decrease when increasing PEG molar mass and content up to 20%, which demonstrates the effectiveness of PEG to act as a plasticizer of PLA.


2013 ◽  
Vol 32 (1) ◽  
pp. 331 ◽  
Author(s):  
Gordana Bogoeva-Gaceva ◽  
Dimko Dimeski ◽  
Vineta Srebrenkoska

In this work, the influence of microfibrillated cellulose (MFC) on the basic mechanical properties of PLA/kenaf fiber biocomposites has been studied. The addition of 5–15 % microfibrillated cellulose to a biocomposite premix has resulted in an increased glass transition temperature of the final product, produced by compression molding of previously melt-mixed composite components. The presence of MFC has influenced the interface-sensitive properties of the PLA/kenaf composite: at an optimal loading of 10 %, the interfacial energy release rate was increased by about 20 %. Moreover, flexural strength and modulus of the composites were also improved (from 34.8 MPa to 57.1 MPa and from 4.9 GPa to 5.8 GPa, respectively).   


CrystEngComm ◽  
2015 ◽  
Vol 17 (30) ◽  
pp. 5651-5663 ◽  
Author(s):  
Chengbo Zhou ◽  
Hongfei Li ◽  
Yao Zhang ◽  
Feifei Xue ◽  
Shaoyong Huang ◽  
...  

The mesocrystal was found to form from the mesophase of glassy PLA stretched below the glass transition temperature.


2021 ◽  
Vol 10 (9) ◽  
pp. e50010916964
Author(s):  
Leticia Riboldi Cavalli ◽  
Jalma Maria Klein ◽  
Ivana Greice Sandri ◽  
Rosmary Brandalise

This work focused on the development of biodegradable active packaging with poly(lactic acid) (PLA), poly(ethylene-co-vinyl acetate) (EVA), polyethylene glycol (PEG) and chitosan (QUI) blends. It investigated thermal and mechanical morphological characteristics of the blends, as the same time, the antifungal activity of the packaging. To assess the antimicrobial activity of the PLA/EVA/PEG/QUI blends, the samples were inserted between slices of bread with no preservative to the evaluation of their shelf life. By comparing between PLA/EVA/PEG, PLA/EVA/PEG/QUI blends and neat PLA was possible to evidence the partial miscibility, decreased glass transition temperature (Tg) by incorporating PEG into the blends, a decrease in flexural strength of 71% and elasticity modulus of 80.4% to PLA/EVA/PEG/2.5QUI blend, as well as an increase in elongation at break of 153% and 392% to impact toughness. A similar behavior was observed to PLA/EVA/20PEG and PLA/EVA/PEG/5.0QUI. The QUI-containing film among the bread slices has also influenced the water activity reduction, and reduced about 35% in the count of molds and yeasts in the slices of bread. Chitosan in mixtures with PLA/EVA/PEG showed potential as a natural antifungal agent in bakery packaging.


2020 ◽  
pp. 2150009
Author(s):  
S. Patra ◽  
K. L. Mohanta ◽  
C. Parida

Modification of surface of natural fibers by high energy electron beam irradiation (6 MeV) is a process for enhancing the adhesion between fiber and matrix. Composites reinforced with natural fiber have gained a prominent place in the field of research and innovation due to the advantages such as low cost, light weight and environment friendly factors. We have studied the thermal properties such as thermal degradation and crystallinity behavior of biodegradable composites using biodegradable polymer poly (lactic) acid (PLA) and fiber of luffa cylindrica (LC) fabricated by using injection molding technique. First, reinforcement LC fibers are irradiated with electron beam of 0.5, 1.0, 2.0, 4.0 and 10.0 Gy using 6 MeV linear accelerator at room temperature in presence of air. The thermal properties like glass transition temperature [Formula: see text], cold crystallization temperature [Formula: see text], melting peak temperature [Formula: see text] and thermal stability of the composites are studied using differential scanning calorimetry (DSC) in the temperature range from 30[Formula: see text]C to 250[Formula: see text]C and thermogravimetric analysis (TGA) in temperature range from 20[Formula: see text]C to 700[Formula: see text]C. The variation of these properties in response to the irradiation dose is analyzed in detail. It is observed that with increase in irradiation dose, glass transition temperature and crystallization temperature increase. However, the thermal stability of the composites is found to increase with increase in irradiation dose.


Author(s):  
M. I. Valueva ◽  
I. V. Zelenina ◽  
M. A. Zharinov ◽  
M. A. Khaskov

The article presents results of studies of experimental carbon plastics based on thermosetting PMRpolyimide binder. Сarbon fiber reinforced plastics (CFRPs) are made from prepregs prepared by melt and mortar technologies, so the rheological properties of the polyimide binder were investigated. The heat resistance of carbon plastics was researched and its elastic-strength characteristics were determined at temperatures up to 320°С. The fundamental possibility of manufacturing carbon fiber from prepregs based on polyimide binder, obtained both by melt and mortar technologies, is shown. CFRPs made from two types of prepregs have a high glass transition temperature: 364°C (melt) and 367°C (solution), with this temperature remaining at the 97% level after boiling, and also at approximately the same (86–97%) level of conservation of elastic strength properties at temperature 300°С.


Polymers ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1734
Author(s):  
Erick Franieck ◽  
Martin Fleischmann ◽  
Ole Hölck ◽  
Larysa Kutuzova ◽  
Andreas Kandelbauer

We report on the cure characterization, based on inline monitoring of the dielectric parameters, of a commercially available epoxy phenol resin molding compound with a high glass transition temperature (>195 °C), which is suitable for the direct packaging of electronic components. The resin was cured under isothermal temperatures close to general process conditions (165–185 °C). The material conversion was determined by measuring the ion viscosity. The change of the ion viscosity as a function of time and temperature was used to characterize the cross-linking behavior, following two separate approaches (model based and isoconversional). The determined kinetic parameters are in good agreement with those reported in the literature for EMCs and lead to accurate cure predictions under process-near conditions. Furthermore, the kinetic models based on dielectric analysis (DEA) were compared with standard offline differential scanning calorimetry (DSC) models, which were based on dynamic measurements. Many of the determined kinetic parameters had similar values for the different approaches. Major deviations were found for the parameters linked to the end of the reaction where vitrification phenomena occur under process-related conditions. The glass transition temperature of the inline molded parts was determined via thermomechanical analysis (TMA) to confirm the vitrification effect. The similarities and differences between the resulting kinetics models of the two different measurement techniques are presented and it is shown how dielectric analysis can be of high relevance for the characterization of the curing reaction under conditions close to series production.


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