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Thermodynamic Behavior of Poly(cyclohexylethylene) in Polyolefin Diblock Copolymers
We report the temperature dependence of the Flory−Huggins interaction parameter for three symmetric diblock copolymer systems containing poly(cyclohexylethylene) (PCHE): poly(cyclohexylethylene-b-ethylene) (CE), poly(cyclohexylethylene-b-ethylethylene) (CEE), and poly(cyclohexylethylene-b-ethylenep...
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Published in: | Macromolecules 2002-09, Vol.35 (19), p.7368-7374 |
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container_title | Macromolecules |
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creator | Cochran, Eric W Bates, Frank S |
description | We report the temperature dependence of the Flory−Huggins interaction parameter for three symmetric diblock copolymer systems containing poly(cyclohexylethylene) (PCHE): poly(cyclohexylethylene-b-ethylene) (CE), poly(cyclohexylethylene-b-ethylethylene) (CEE), and poly(cyclohexylethylene-b-ethylenepropylene) (CP). Order−disorder transition temperatures (T ODT) were determined using dynamic mechanical spectroscopy and interpreted with mean-field theory, (χN)ODT = 10.5, leading to well-defined expressions for χ(T). These results have been analyzed in the context of solubility parameter (δ) theory resulting in a unique parameter δC that describes the interactions in CE, CP, and CEE, where δC < δE E < δP < δE with (δE − δC) ≈ 1.6 MPa1/2 at 500 K. In contrast to the predictions of group contribution theory, this indicates that δC is in surprisingly close proximity to the solubility parameter for poly(dimethylsiloxane). |
doi_str_mv | 10.1021/ma020227+ |
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Order−disorder transition temperatures (T ODT) were determined using dynamic mechanical spectroscopy and interpreted with mean-field theory, (χN)ODT = 10.5, leading to well-defined expressions for χ(T). These results have been analyzed in the context of solubility parameter (δ) theory resulting in a unique parameter δC that describes the interactions in CE, CP, and CEE, where δC < δE E < δP < δE with (δE − δC) ≈ 1.6 MPa1/2 at 500 K. 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Order−disorder transition temperatures (T ODT) were determined using dynamic mechanical spectroscopy and interpreted with mean-field theory, (χN)ODT = 10.5, leading to well-defined expressions for χ(T). These results have been analyzed in the context of solubility parameter (δ) theory resulting in a unique parameter δC that describes the interactions in CE, CP, and CEE, where δC < δE E < δP < δE with (δE − δC) ≈ 1.6 MPa1/2 at 500 K. 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Order−disorder transition temperatures (T ODT) were determined using dynamic mechanical spectroscopy and interpreted with mean-field theory, (χN)ODT = 10.5, leading to well-defined expressions for χ(T). These results have been analyzed in the context of solubility parameter (δ) theory resulting in a unique parameter δC that describes the interactions in CE, CP, and CEE, where δC < δE E < δP < δE with (δE − δC) ≈ 1.6 MPa1/2 at 500 K. In contrast to the predictions of group contribution theory, this indicates that δC is in surprisingly close proximity to the solubility parameter for poly(dimethylsiloxane).</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/ma020227+</doi><tpages>7</tpages></addata></record> |
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subjects | Applied sciences Exact sciences and technology Organic polymers Physicochemistry of polymers Properties and characterization Thermal and thermodynamic properties |
title | Thermodynamic Behavior of Poly(cyclohexylethylene) in Polyolefin Diblock Copolymers |
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