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    The Role of Gas Dissolution and Induced Crystallization During Microcellular Polymer Processing: A Study of Poly (Ethylene Terephthalate) and Carbon Dioxide Systems

    Source: Journal of Engineering Materials and Technology:;1995:;volume( 117 ):;issue: 001::page 62
    Author:
    Daniel F. Baldwin
    ,
    Minuro Shimbo
    ,
    Nam P. Suh
    DOI: 10.1115/1.2804373
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: One of the critical steps in the production of microcellular polymers is the dissolution of gas into a polymer matrix. In this paper, the formation of a gas and semi-crystalline thermoplastic solution is studied in the presence of a crystallizing matrix with particular emphasis on the ultimate effects of crystallinity on microcellular polymer processing. In this particular study, carbon dioxide was selected as the gas and poly (ethylene terephthalate) (PET) as the polymer. Polymer/gas solution formation is the precursor to the microvoid nucleation and growth during microcellular polymer processing. In batch processing, the solution formation is typically accomplished by placing a polymer sample in a high pressure gas environment resulting in the diffusion of gas into the polymer matrix. For gas and semi-crystalline thermoplastic systems, the solution formation process is notably more complex. In particular, PET crystallizes in the presence of high Co2 solution concentrations. The crystallization results in a solution that is relatively difficult to microcellular process, requiring relatively high temperatures as compared to amorphous polymer/gas solutions. However, the resulting crystalline foam has a superior microcellular morphology. In addition, the crystallization of the solution results in a lower solubility, an increased matrix stiffness, and a lower diffusivity. Our analysis includes (1) an experimental characterization of the carbon dioxide-induced crystallization occurring during microcellular polymer processing, indicating a critical gas concentration is required for crystallization, (2) an experimental estimation of the vis-coelastic behavior of amorphous and semi-crystalline PET/CO2 solutions, and (3) an experimental investigation of the effects of crystallinity on microcellular processing and the resulting cell morphology. Crystallinity was found to play a major role in microcellular processing through its effects on (a) cell nucleation mechanisms resulting in larger cell densities due to heterogeneous nucleation at the amorphous/crystalline boundaries and (b) cell growth mechanisms resulting in smaller cell sizes due to the increased matrix stiffness of the semi-crystalline matrix.
    keyword(s): Crystallization , Polymers , Carbon dioxide , Nucleation (Physics) , Stiffness , Mechanisms , Diffusion (Physics) , High temperature , Experimental characterization , Carbon AND High pressure (Physics) ,
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      The Role of Gas Dissolution and Induced Crystallization During Microcellular Polymer Processing: A Study of Poly (Ethylene Terephthalate) and Carbon Dioxide Systems

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    http://yetl.yabesh.ir/yetl1/handle/yetl/115429
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    contributor authorDaniel F. Baldwin
    contributor authorMinuro Shimbo
    contributor authorNam P. Suh
    date accessioned2017-05-08T23:47:23Z
    date available2017-05-08T23:47:23Z
    date copyrightJanuary, 1995
    date issued1995
    identifier issn0094-4289
    identifier otherJEMTA8-26969#62_1.pdf
    identifier urihttp://yetl.yabesh.ir/yetl/handle/yetl/115429
    description abstractOne of the critical steps in the production of microcellular polymers is the dissolution of gas into a polymer matrix. In this paper, the formation of a gas and semi-crystalline thermoplastic solution is studied in the presence of a crystallizing matrix with particular emphasis on the ultimate effects of crystallinity on microcellular polymer processing. In this particular study, carbon dioxide was selected as the gas and poly (ethylene terephthalate) (PET) as the polymer. Polymer/gas solution formation is the precursor to the microvoid nucleation and growth during microcellular polymer processing. In batch processing, the solution formation is typically accomplished by placing a polymer sample in a high pressure gas environment resulting in the diffusion of gas into the polymer matrix. For gas and semi-crystalline thermoplastic systems, the solution formation process is notably more complex. In particular, PET crystallizes in the presence of high Co2 solution concentrations. The crystallization results in a solution that is relatively difficult to microcellular process, requiring relatively high temperatures as compared to amorphous polymer/gas solutions. However, the resulting crystalline foam has a superior microcellular morphology. In addition, the crystallization of the solution results in a lower solubility, an increased matrix stiffness, and a lower diffusivity. Our analysis includes (1) an experimental characterization of the carbon dioxide-induced crystallization occurring during microcellular polymer processing, indicating a critical gas concentration is required for crystallization, (2) an experimental estimation of the vis-coelastic behavior of amorphous and semi-crystalline PET/CO2 solutions, and (3) an experimental investigation of the effects of crystallinity on microcellular processing and the resulting cell morphology. Crystallinity was found to play a major role in microcellular processing through its effects on (a) cell nucleation mechanisms resulting in larger cell densities due to heterogeneous nucleation at the amorphous/crystalline boundaries and (b) cell growth mechanisms resulting in smaller cell sizes due to the increased matrix stiffness of the semi-crystalline matrix.
    publisherThe American Society of Mechanical Engineers (ASME)
    titleThe Role of Gas Dissolution and Induced Crystallization During Microcellular Polymer Processing: A Study of Poly (Ethylene Terephthalate) and Carbon Dioxide Systems
    typeJournal Paper
    journal volume117
    journal issue1
    journal titleJournal of Engineering Materials and Technology
    identifier doi10.1115/1.2804373
    journal fristpage62
    journal lastpage74
    identifier eissn1528-8889
    keywordsCrystallization
    keywordsPolymers
    keywordsCarbon dioxide
    keywordsNucleation (Physics)
    keywordsStiffness
    keywordsMechanisms
    keywordsDiffusion (Physics)
    keywordsHigh temperature
    keywordsExperimental characterization
    keywordsCarbon AND High pressure (Physics)
    treeJournal of Engineering Materials and Technology:;1995:;volume( 117 ):;issue: 001
    contenttypeFulltext
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