Quasi‐chemical approximation for nonrandomness in the hole theory of polymeric systems: Application to homopolymer/random copolymer blends
Hankun Xie, Erík Nies
Abstract
Hankun Xie, Erík Nies
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.
OpenAlex reports 4 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
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