scholarly journals Nonisothermal Crystallization of Surface-Treated Alumina and Aluminum Nitride-Filled Polylactic Acid Hybrid Composites

Polymers ◽  
2019 ◽  
Vol 11 (6) ◽  
pp. 1077 ◽  
Author(s):  
Zelalem Lule ◽  
Jooheon Kim
Keyword(s):  
Aluminum Nitride ◽  
Polylactic Acid ◽  
Hybrid Composites ◽  
Crystallization Rate ◽  
Degree Of Crystallinity ◽  
Crystal Formation ◽  
Scanning Calorimetry ◽  
Nonisothermal Crystallization ◽  
Avrami Model ◽  
Filler Particles

This work investigates the nonisothermal crystallization and melting behavior of polylactic acid (PLA), filled with treated and untreated alumina and nano-aluminum nitride hybrid composites. Analysis by attenuated total reflectance Fourier transform infrared spectroscopy revealed that the treated fillers and the PLA matrix developed a good interaction. The crystallization and melting behaviors of the PLA hybrid composites were investigated using differential scanning calorimetry showed that the degree of crystallinity increased with the addition of hybrid fillers. Unlike the untreated PLA composites, the complete crystallization of the treated PLA hybrid composites hindered cold crystallization during the second heating cycle. The crystallization kinetics studied using the Avrami model indicated that the crystallization rate of PLA was affected by the inclusion of filler particles. X-ray diffraction analysis confirmed crystal formation with the incorporation of filler particles. The inclusion of nano-aluminum nitride (AlN) and the increase in the crystallinity led to an improvement of the storage modulus.

scholarly journals Mechanical Strength Enhancement of Polylactic Acid Hybrid Composites

Polymers ◽  
2019 ◽  
Vol 11 (2) ◽  
pp. 349 ◽  
Author(s):  
Ji-Won Park ◽  
Jae-Ho Shin ◽  
Gyu-Seong Shim ◽  
Kyeng-Bo Sim ◽  
Seong-Wook Jang ◽  
...  
Keyword(s):  
Composite Material ◽  
Mechanical Strength ◽  
Polylactic Acid ◽  
Mechanical Performance ◽  
Natural Fiber ◽  
Hybrid Composites ◽  
Structural Characteristics ◽  
Scanning Calorimetry ◽  
Environmental Friendliness ◽  
Research Attention

In recent years, there has been an increasing need for materials that are environmentally friendly and have functional properties. Polylactic acid (PLA) is a biomass-based polymer, which has attracted research attention as an eco-friendly material. Various studies have been conducted on functionality imparting and performance improvement to extend the field of application of PLA. Particularly, research on natural fiber-reinforced composites have been conducted to simultaneously improve their environmental friendliness and mechanical strength. Research interest in hybrid composites using two or more fillers to realize multiple functions are also increasing. Phase change materials (PCMs) absorb and emit energy through phase transition and can be used as a micro encapsulated structure. In this study, we fabricated hybrid composites using microcapsulated PCM (MPCM) and the natural fibrous filler, kenaf. We aimed to fabricate a composite material with improved endothermic characteristics, mechanical performance, and environmental friendliness. We analyzed the endothermic properties of MPCM and the structural characteristics of two fillers and finally produced an eco-friendly composite material. The PCM and kenaf contents were varied to observe changes in the performance of the hybrid composites. The endothermic properties were determined through differential scanning calorimetry, whereas changes in the physical properties of the hybrid composite were determined by measuring the mechanical properties.

Effect of Crystallinity on the Performance of P3HT/PC70BM/n-Dodecylthiol Polymer Solar Cells

2013 ◽  
Vol 136 (2) ◽  
Author(s):  
Nidal Abu-Zahra ◽  
Mahmoud Algazzar
Keyword(s):  
Solar Cells ◽  
Power Conversion Efficiency ◽  
Conversion Efficiency ◽  
Polymer Solar Cells ◽  
Short Circuit ◽  
Power Conversion ◽  
Crystallization Rate ◽  
Short Circuit Current ◽  
Scanning Calorimetry ◽  
Avrami Model

In this research, n-dodecylthiol was added to P3HT/PC70BM polymer solar cells (PSCs) to improve the crystallinity of P3HT and enhance the phase separation of P3HT/PC70BM. Crystallinity of P3HT:PC70BM doped with 0–5% by volume of n-dodecylthiol was measured using X-ray diffraction (XRD) and differential scanning calorimetry (DSC) techniques. Both methods showed improvement in crystallinity, which resulted in improving the power conversion efficiency (PCE) of polymer solar cells by 33%. In addition, annealing at 150 °C for 30 min showed further improvement in crystallinity with n-dodecylthiol concentration up to 2%. The highest power conversion efficiency of 3.21% was achieved with polymer crystallites size L of 11.2 nm, after annealing at 150 °C for 30 min under a vacuum atmosphere. The smaller crystallite size suggests a shorter path of the charge carriers between P3HT backbones, which could be beneficial to getting a higher short circuit current in the devices made with the additive. Kinetics study of P3HT:PC70BM crystallinity using Avrami model showed a faster crystallization rate (1/t0.5) at higher temperatures.

Crystallization Processes In Poly (Ethylene Terephthalate) / Polycarbonate Blends

1993 ◽  
Vol 321 ◽  
Author(s):  
Veronika E. Reinsch ◽  
Ludwig Rebenfeld
Keyword(s):  
Ethylene Terephthalate ◽  
Crystallization Rate ◽  
Melt Processing ◽  
Degree Of Crystallinity ◽  
Processing Temperature ◽  
Scanning Calorimetry ◽  
Processing Times ◽  
Poly Ethylene Terephthalate ◽  
Poly Ethylene ◽  
Crystallization From The Melt

ABSTRACTBlends of poly (ethylene terephthalate), or PET, and polycarbonate (PC) over a range of compositions were studied in isothermal crystallizations from the melt using differential scanning calorimetry (DSC). Both crystallization rate and degree of crystallinity of PET depend on blend composition. The glass transition temperature, Tg, of PET and PC in blends and pure polymer were also measured by DSC. Elevation of the Tg of PET and depression of the Tg of PC are observed upon blending. In cooling scans, dynamic crystallization from the melt was observed. In PET/PC blends with high PC content, a novel dual-peak crystallization of PET was observed. The effects of thermal history on crystallization kinetics and degree of crystallinity were also determined in isothermal crystallization studies. For Melt processing times between 1 and 30 Min and for processing temperatures between 280 and 300 °C, Melt processing temperature was seen to have a stronger effect than processing time.

scholarly journals Combined Effects of Cellulose Nanofiber Nucleation and Maleated Polylactic Acid Compatibilization on the Crystallization Kinetic and Mechanical Properties of Polylactic Acid Nanocomposite

Polymers ◽  
2021 ◽  
Vol 13 (19) ◽  
pp. 3226
Author(s):  
Siti Shazra Shazleen ◽  
Lawrence Yee Foong Ng ◽  
Nor Azowa Ibrahim ◽  
Mohd Ali Hassan ◽  
Hidayah Ariffin
Keyword(s):  
Mechanical Properties ◽  
Tensile Strength ◽  
Polylactic Acid ◽  
Crystallization Kinetics ◽  
Crystallization Kinetic ◽  
Crystallization Rate ◽  
Combined Effects ◽  
Dsc Analysis ◽  
Scanning Calorimetry ◽  
Isothermal Crystallization Kinetics

This work investigated the combined effects of CNF nucleation (3 wt.%) and PLA-g-MA compatibilization at different loadings (1–4 wt.%) on the crystallization kinetics and mechanical properties of polylactic acid (PLA). A crystallization kinetics study was done through isothermal and non-isothermal crystallization kinetics using differential scanning calorimetry (DSC) analysis. It was shown that PLA-g-MA had some effect on nucleation as exhibited by the value of crystallization half time and crystallization rate of the PLA/PLA-g-MA, which were increased by 180% and 172%, respectively, as compared to neat PLA when isothermally melt crystallized at 100 °C. Nevertheless, the presence of PLA-g-MA in PLA/PLA-g-MA/CNF3 nanocomposites did not improve the crystallization rate compared to that of uncompatibilized PLA/CNF3. Tensile strength was reduced with the increased amount of PLA-g-MA. Contrarily, Young’s modulus values showed drastic increment compared to the neat PLA, showing that the addition of the PLA-g-MA contributed to the rigidity of the PLA nanocomposites. Overall, it can be concluded that PLA/CNF nanocomposite has good performance, whereby the addition of PLA-g-MA in PLA/CNF may not be necessary for improving both the crystallization kinetics and tensile strength. The addition of PLA-g-MA may be needed to produce rigid nanocomposites; nevertheless, in this case, the crystallization rate of the material needs to be compromised.

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 Degradation of Polylactic Acid Using Sub-Critical Water for Compost

Polymers ◽  
2020 ◽  
Vol 12 (11) ◽  
pp. 2434
Author(s):  
Toshiharu Goto ◽  
Mikitaka Kishita ◽  
Yin Sun ◽  
Takeshi Sako ◽  
Idzumi Okajima
Keyword(s):  
Molecular Weight ◽  
Polylactic Acid ◽  
Food Packaging ◽  
Crystallization Rate ◽  
General Purpose ◽  
Water Soluble ◽  
Decomposition Rates ◽  
Scanning Calorimetry ◽  
Reaction Conditions ◽  
Decomposition Products

Polylactic acid (PLA) is expected to replace many general-purpose plastics, especially those used for food packaging and agricultural mulch. In composting, the degradation speed of PLA is affected by the molecular weight, crystallinity, and microbial activity. PLA with a molecular weight of less than 10,000 has been reported to have higher decomposition rates than those with higher molecular weight. However, PLA degradation generates water-soluble products, including lactic acid, that decrease the pH of soil or compost. As acidification of soil or compost affects farm products, their pH should be controlled. Therefore, a method for determining suitable reaction conditions to achieve ideal decomposition products is necessary. This study aimed to determine suitable reaction conditions for generating preprocessed PLA with a molecular weight lower than 10,000 without producing water-soluble contents. To this end, we investigated the degradation of PLA using sub-critical water. The molecular weight and ratio of water-soluble contents (WSCs) affecting the pH of preprocessed products were evaluated through kinetic analysis, and crystallinity was analyzed through differential scanning calorimetry. Preprocessed PLA was prepared under the determined ideal conditions, and its characteristics in soil were observed. The results showed that the crystallization rate increased with PLA decomposition but remained lower than 30%. In addition, the pH of compost mixed with 40% of preprocessed PLA could be controlled within pH 5.4–5.5 over 90 days. Overall, soil mixed with the preprocessed PLA prepared under the determined ideal conditions remains suitable for plant growth.

Parameters characterizing the kinetics of the non-isothermal crystallization of polyamide 5,6 determined by differential scanning calorimetry

2014 ◽  
Vol 34 (4) ◽  
pp. 353-358 ◽  
Author(s):  
Yassir A. Eltahir ◽  
Haroon A.M. Saeed ◽  
Chen Yuejun ◽  
Yumin Xia ◽  
Wang Yimin
Keyword(s):  
Crystallization Kinetics ◽  
Isothermal Crystallization ◽  
Crystallization Rate ◽  
Degree Of Crystallinity ◽  
Avrami Equation ◽  
Scanning Calorimetry ◽  
Isothermal Crystallization Kinetics ◽  
Ozawa Model ◽  
Kinetic Crystallization ◽  
Kinetics Of

Abstract The non-isothermal crystallization behavior of polyamide 5,6 (PA56) was investigated by differential scanning calorimeter (DSC), and the non-isothermal crystallization kinetics were analyzed using the modified Avrami equation, the Ozawa model, and the method combining the Avrami and Ozawa equations. It was found that the Avrami method modified by Jeziorny could only describe the primary stage of non-isothermal crystallization kinetics of PA56, the Ozawa model failed to describe the non-isothermal crystallization of PA56, while the combined approach could successfully describe the non-isothermal crystallization process much more effectively. Kinetic parameters, such as the Avrami exponent, kinetic crystallization rate constant, relative degree of crystallinity, the crystallization enthalpy, and activation energy, were also determined for PA56.

Effect of Poly(D-Lactic Acid)-co-Polyethylene Glycol on the Crystallization of Poly(L-Lactic Acid)

2017 ◽  
Vol 751 ◽  
pp. 283-289 ◽  
Author(s):  
Ployrawee Kaewlamyai ◽  
Amornrat Lertworasirikul
Keyword(s):  
Lactic Acid ◽  
Polyethylene Glycol ◽  
Weight Ratio ◽  
Crystallization Rate ◽  
Heat Stability ◽  
Nucleating Agent ◽  
Degree Of Crystallinity ◽  
Poly Lactic Acid ◽  
Infrared Spectrometry ◽  
Scanning Calorimetry

Poly (lactic acid) (PLA) is a biopolymer derived from renewable resources and can be disposed of without creating harm to the environment. PLA can be formed by thermoplastic processes and has good mechanical properties. However, its disadvantages are a high crystallization temperature, slow crystallization rate, poor heat stability and low ductility. In the past, it was found that poly (D-lactic acid) (PDLA) can form complexes with poly (L-lactic acid) (PLLA) and the complexes could accelerate the crystallization and increase the degree of crystallinity of the PLA, but decrease the ductility. It is known that polyethylene glycol (PEG) can improve the ductility of PLLA. In this research, PDLA was copolymerized with PEG in an attempt to improve both crystallization behavior and ductility of PLLA. Poly (D-lactic acid)-co-polyethylene glycol (PDEG) was synthesized by ring opening polymerization using D-lactide and PEG at a D-lactide:PEG weight ratio of 10:3. The PDEG was blended with PLLA with a PDEG content of 0wt% to 50wt% by melt blending process. Fourier transform infrared spectrometry (FT-IR) and X-Ray diffractometry (XRD) confirmed the stereocomplex formation between PDEG and PLLA. Characterization by differential scanning calorimetry (DSC) revealed that crystallization temperatures of the blends were decreased in the presence of PDEG. Storage moduli and tan of the blends obtained from dynamic mechanical analysis (DMA) decreased as PDEG content increased. Polarized optical microscopy (POM) micrographs of blends with PDEG content of 1wt% to 5wt% obviously showed that crystallization rate was increased. PDEG has the potential to be an effective nucleating agent and efficient plasticizer for PLLA.

scholarly journals An insight on the process–property relationships of melt spun polylactic acid fibers

2019 ◽  
Vol 89 (23-24) ◽  
pp. 4959-4966 ◽  
Author(s):  
AM Ali ◽  
HM El-Dessouky
Keyword(s):  
Polylactic Acid ◽  
High Performance ◽  
Polarized Light ◽  
Degree Of Crystallinity ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Laser Diffractometry ◽  
Wide Range ◽  
Innovative Materials ◽  
The Degree Of Crystallinity

Polylactic acid (PLA) fibers are receiving growing interest as one of the recent innovative materials being developed for various applications. The inherent biodegradability of PLA makes it highly attractive for the biomedical and health care sectors. PLA fibers need to be partially and/or highly oriented to allow high performance and readiness for a wide range of manufacturability. In this study, the structure and properties of PLA fibers, manufactured at different spinning speeds, were studied. Laser diffractometry, polarized light microscopy, differential scanning calorimetry (DSC) and X-ray diffraction (XRD) were used to determine the diameter, birefringence, molecular orientation, enthalpy and degree of crystallinity of as-spun and drawn PLA fibers. The results of DSC and XRD showed that the degree of crystallinity of the PLA fibers is significantly improved for the drawn PLA fibers compared to the as-spun fibers and leveled off in the case of changing the take-up speeds of drawn fibers.

scholarly journals Synthesis and Nonisothermal Crystallization Kinetics of Poly(Butylene Terephthalate-co-Tetramethylene Ether Glycol) Copolyesters

Polymers ◽  
2020 ◽  
Vol 12 (9) ◽  
pp. 1897 ◽  
Author(s):  
Hsu-I Mao ◽  
Chin-Wen Chen ◽  
Syang-Peng Rwei
Keyword(s):  
Crystallization Rate ◽  
Resonance Spectroscopy ◽  
Scanning Calorimetry ◽  
Nonisothermal Crystallization ◽  
Excellent Thermal Stability ◽  
Butylene Terephthalate ◽  
Melt Polymerization ◽  
Ft Ir ◽  
Nonisothermal Crystallization Kinetics ◽  
Kinetics Of

Poly(butylene terephthalate-co-tetramethylene ether glycol) (PBT-co-PTMEG) copolymers with PTMEG ranging from 0 to 40 wt% were synthesized through melt polymerization. The structure and composition were supported by Fourier-transform infrared spectroscopy (FT-IR) and nuclear magnetic resonance spectroscopy (1H NMR). All samples had excellent thermal stability at a Td−5% around 370 °C. Crystallization temperature (Tc) and enthalpy of crystallization (ΔHc) were detected by differential scanning calorimetry (DSC), revealing a decrement from 182.3 to 135.1 °C and 47.0 to 22.1 J g−1, respectively, with the increase in PTMEG concentration from 0 to 40 wt%. Moreover, nonisothermal crystallization was carried out to explore the crystallization behavior of copolymers; the crystallization rate of PBT reduced gradually when PTMEG content increased. Hence, a decrement in the spherulite growth rate was detected in polarizing light microscope (PLM) observation, observing that the PTMEG could enhance the hindrance in the molecular chain to lower the crystallinity of PBT-co-PTMEG copolyester. Moreover, thermal properties and the crystallization rate of PBT-co-PTMEG copolymers can be amended via the regulation of PTMEG contents.

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