1992•Makromolekulare Chemie Macromolecular SymposiaOpen access

Quasi‐chemical approximation for nonrandomness in the hole theory of polymeric systems: Application to homopolymer/random copolymer blends

Hankun Xie, Erík Nies

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Abstract

Abstract The non‐random‐mixing version of the Holey‐Huggins theory is used to extract molecular parameters from the experimental equation of state data of polystyrene, poly(p‐bromostyrene) and a random copolymer poly(styrene‐co‐p‐bromostyrene) of known composition. With these parameters upper critical miscibility behavior, in qualitative agreement with experimental observations, is predicted for the system poly(styrene‐co‐p‐bromostyrene)/polystyrene. Quantitative agreement can be obtained for the equation of state and miscibility behavior if small changes in the values of the cross parameters are allowed.

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What this paper is about

Abstract The non‐random‐mixing version of the Holey‐Huggins theory is used to extract molecular parameters from the experimental equation of state data of polystyrene, poly(p‐bromostyrene) and a random copolymer poly(styrene‐co‐p‐bromostyrene) of known composition. With these parameters upper critical miscibility behavior, in qualitative agreement with experimental observations, is predicted for the system poly(styrene‐co‐p‐bromostyrene)/polystyrene. Quantitative agreement can be obtained for the equation of state and miscibility behavior if small changes in the values of the cross parameters are allowed.

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Available abstract

Abstract The non‐random‐mixing version of the Holey‐Huggins theory is used to extract molecular parameters from the experimental equation of state data of polystyrene, poly(p‐bromostyrene) and a random copolymer poly(styrene‐co‐p‐bromostyrene) of known composition. With these parameters upper critical miscibility behavior, in qualitative agreement with experimental observations, is predicted for the system poly(styrene‐co‐p‐bromostyrene)/polystyrene. Quantitative agreement can be obtained for the equation of state and miscibility behavior if small changes in the values of the cross parameters are allowed.

Key concepts: Miscibility, Copolymer, Polystyrene, Styrene, Materials science, Flory–Huggins solution theory, Polymer chemistry, Random phase approximation

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