Unravelling the effects of size, volume fraction and shape of nanoparticle additives on crystallization of nanocomposite polymers

Jabbarzadeh, Ahmad; Halfina, Beny

doi:10.1039/c9na00525k

Cited by 38 publications

(29 citation statements)

References 43 publications

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“…According to Table 2 ,

is equal to 1.829 in (a) and is equal to 2.491 in (b), it shows that PEG and the PEG block in PEG-PLLA during the crystallization process differed by about one dimension under the same cooling method, and further illustrates that the first crystallized PLLA block have an effect of the crystallization behavior on the later crystallized PEG block. Specifically, the crystal of the PLLA block provides nucleating sites for the crystallization of the PEG block and can be regarded as heterogeneous nucleation to a certain extent [ 7 , 22 ]. The difference of

between (b) and (c) means that inhibition of crystallization in the PLLA block has a significant effect on subsequent crystallization.…”

Section: Resultsmentioning

confidence: 99%

“…Understanding and controlling the crystallization behavior have provided an effective method for predicting and adjusting the physical properties of crystalline polymers. In addition, just as the additive nanoparticles have an influence on the crystallization of nanocomposite polymers, the crystallization of different blocks in the double-crystallizable block copolymer PEG-PLLA is bound to influence each element, which is worth exploring [ 7 , 8 , 9 ].…”

Section: Introductionmentioning

confidence: 99%

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Non-Isothermal Crystallization Kinetics of Poly(Ethylene Glycol)–Poly(l-Lactide) Diblock Copolymer and Poly(Ethylene Glycol) Homopolymer via Fast-Scan Chip-Calorimeter

et al. 2021

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The non-isothermal crystallization kinetics of double-crystallizable poly(ethylene glycol)–poly(l-lactide) diblock copolymer (PEG-PLLA) and poly(ethylene glycol) homopolymer (PEG) were studied using the fast cooling rate provided by a Fast-Scan Chip-Calorimeter (FSC). The experimental data were analyzed by the Ozawa method and the Kissinger equation. Additionally, the total crystallization rate was represented by crystallization half time t1/2. The Ozawa method is a perfect success because secondary crystallization is inhibited by using fast cooling rate. The first crystallized PLLA block provides nucleation sites for the crystallization of PEG block and thus promotes the crystallization of the PEG block, which can be regarded as heterogeneous nucleation to a certain extent, while the method of the PEG block and PLLA block crystallized together corresponds to a one-dimensional growth, which reflects that there is a certain separation between the crystallization regions of the PLLA block and PEG block. Although crystallization of the PLLA block provides heterogeneous nucleation conditions for PEG block to a certain extent, it does not shorten the time of the whole crystallization process because of the complexity of the whole crystallization process including nucleation and growth.

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“…According to Table 2 ,

between (b) and (c) means that inhibition of crystallization in the PLLA block has a significant effect on subsequent crystallization.…”

Section: Resultsmentioning

confidence: 99%

Section: Introductionmentioning

confidence: 99%

Non-Isothermal Crystallization Kinetics of Poly(Ethylene Glycol)–Poly(l-Lactide) Diblock Copolymer and Poly(Ethylene Glycol) Homopolymer via Fast-Scan Chip-Calorimeter

et al. 2021

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“…The potential for using composite materials has been widely reported in different application fields [ 22 , 23 , 24 ]. In the case of hybrid polymeric systems, the control of crystallinity has a great impact on their properties and is fundamental for developing innovative functional materials [ 23 ].…”

Section: Resultsmentioning

confidence: 99%

“…In the case of hybrid polymeric systems, the control of crystallinity has a great impact on their properties and is fundamental for developing innovative functional materials [ 23 ]. Moreover, the effects of volume fraction, size, and shape of the reinforcement on the composite properties have been largely stressed [ 24 ].…”

Section: Resultsmentioning

confidence: 99%

Stress Distributions for Hybrid Composite Endodontic Post Designs with and without a Ferrule: FEA Study

et al. 2020

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The aim of the current work was to analyze the influence of the ferrule effect for hybrid composite endodontic post designs consisting of carbon (C) and glass (G) fiber-reinforced polyetherimide (PEI), in upper canine teeth. Starting from theoretical designs of C-G/PEI hybrid composite posts with different Young’s moduli (Post A—57.7 GPa, Post B—31.6 GPa, Post C—graduated from 57.7 to 9.0 GPa in the coronal–apical direction) in endodontically treated anterior teeth, the influence of the ferrule effect was determined through finite element analysis (FEA). On the surface of the crown, a load of 50 N was applied at 45° to the longitudinal axis of the tooth. Maximum principal stresses were evaluated along the C-G/PEI post as well as at the interface between the surrounding tooth structure and the post. Maximum stress values were lower than those obtained for the corresponding models without a ferrule. The presence of a ferrule led to a marked decrease of stress and gradients especially for posts A and B. A less marked effect was globally found for Post C, except in a cervical margin section along a specific direction, where a significant decrease of the stress was probably due to local geometric features, compared to the model without a ferrule. The presence of a ferrule did not generally provide a marked benefit in the case of the graduated Post C, in comparison to other C-G/PEI posts. The outcomes suggest how such a hybrid composite post alone should be sufficient to optimize the stress distribution, dissipating stress from the coronal to the apical end.

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“…The results of large-scale molecular dynamics simulations revealed that while crystallinity was affected by the nanoparticle size and its volume fraction, their combined effects can only be measured by interparticle free space and the characteristic size of the crystals. Understanding the dynamics of these systems, including the mobilities of the different constituents, also remains an extremely difficult task, despite the wide-ranging research interest in them [ 20 , 21 ].…”

Section: Introductionmentioning

confidence: 99%

Nanocomposite Materials with Poly(l-lactic Acid) and Transition-Metal Dichalcogenide Nanosheets 2D-TMDCs WS2

et al. 2020

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Layered transition-metal dichalcogenides (TMDCs) based on tungsten disulfide nanosheets (2D-WS2) were introduced via melt processing into poly(l-lactic acid) (PLLA) to generate PLLA/2D-WS2 nanocomposite materials. The effects of the 2D-WS2 on the morphology, crystallization, and biodegradation behavior of PLLA were investigated. In particular, the non-isothermal melt-crystallization of neat PLLA and PLLA/2D-WS2 nanocomposites were analyzed in detail by varying both the cooling rate and 2D-WS2 loading. The kinetic parameters of PLLA chain crystallization are successfully described using the Liu model. It was found that the PLLA crystallization rate was reduced with 2D-WS2 incorporation, while the crystallization mechanism and crystal structure of PLLA remained unchanged in spite of nanoparticle loading. This was due to the PLLA chains not being able to easily adsorb on the WS2 nanosheets, hindering crystal growth. In addition, from surface morphology analysis, it was observed that the addition of 2D-WS2 facilitated the enzymatic degradation of poorly biodegradable PLLA using a promising strain of actinobacteria, Lentzea waywayandensis. The identification of more suitable enzymes to break down PLLA nanocomposites will open up new avenues of investigation and development, and it will also lead to more environmentally friendly, safer, and economic routes for bioplastic waste management.

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Unravelling the effects of size, volume fraction and shape of nanoparticle additives on crystallization of nanocomposite polymers

Cited by 38 publications

References 43 publications

Non-Isothermal Crystallization Kinetics of Poly(Ethylene Glycol)–Poly(l-Lactide) Diblock Copolymer and Poly(Ethylene Glycol) Homopolymer via Fast-Scan Chip-Calorimeter

Non-Isothermal Crystallization Kinetics of Poly(Ethylene Glycol)–Poly(l-Lactide) Diblock Copolymer and Poly(Ethylene Glycol) Homopolymer via Fast-Scan Chip-Calorimeter

Stress Distributions for Hybrid Composite Endodontic Post Designs with and without a Ferrule: FEA Study

Nanocomposite Materials with Poly(l-lactic Acid) and Transition-Metal Dichalcogenide Nanosheets 2D-TMDCs WS2

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