• Title/Summary/Keyword: Themodynamic parameter

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Phase Separations in Random Copolymer Solutions by Continuous Thermodynamics (연속열역학을 이용한 랜덤공중합체 용액의 상분리)

  • Sheo, Shin-Ho;Kim, Ki-Chang;Lee, Kwang-Rae
    • Journal of Industrial Technology
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    • v.18
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    • pp.277-287
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    • 1998
  • In this work continuous thermodynamics was adopted for describing the influence of copolymer polydispersity on phase separations in random copolymer solutions. Continuous themodynamic frameworks were formulated using the Flory-Huggin's excess Gibbs free energy model in which the concentration- and temperature-depentent terms of interaction parameter x were modified. Cloud-point curves and coexistence curves of poly(ethylene-vinylactate)/methylacetate solutions and poly(ehtylene-vinylacetate)/ethylacetate solutions were measured, and experimental data were fitted with theoretical relations formulated in this work. Calculated could-point curves were more good ageeable with experimental data than the modified Flory-Huggins's relations. Coexistence curves which were evaluated by using parameters of x estimated from experimental cloud-point curves, were found to coincide with experimental data.

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The Interpratation of Dyeing Behavior of the Easily Dyeable Polyester Yarn under Atmospheric Pressure by Thermodynamic Parameters (열역학적 파라미터에 의한 상압가염형 폴리에스테르 섬유의 염색거동 해석)

  • 김태경;윤석한;신상엽;임용진;조규민
    • Textile Coloration and Finishing
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    • v.14 no.1
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    • pp.51-57
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    • 2002
  • In the prior study, the mechanical properties and the dyeability of the easily dyeable polyester grim(EDY) were investigated. In this study, to interpret the dyeing behavior of EDY with C. I. Disperse Violet 1, the thermodynamic parameters of dyeing, such as the standard affinity, the heat of dyeing(the enthalpy change), the entropy change, the diffusion coefficient, and the activation energy of diffusion, were obtained from adsorption isotherms and dyeing rate at various temperatures and compared to these of regular polyester (REG-PET). The heat of dyeing(the enthalpy change) and the entropy change for EDY showed smaller negative values than those for REG-PET. This means that the dye molecules in the EDY are combined more loosely than in the REG-PET and that is due to the flexibility of polymer chains of EDY. The diffusion coefficients of C. I. Disperse Violet 1 into the EDY were larger than those for REG-PET, and the activation energy of diffusion on EDY was smaller than that on REG-PET.