1995Collection of Czechoslovak Chemical CommunicationsRequires access

Liquid-Liquid Phase Separation in Multicomponent Polymer Systems. XXVI. Blends of Two Polydisperse Polymers

Karel Šolc, R. Koningsveld

Open publisher page 16 citations

Abstract

A method for computing phase diagrams of polydisperse A/B polymer blends is proposed, based on Flory-Huggins-Staverman thermodynamics, and employed to obtain cloud-point curves (CPCs), shadow curves, spinodals and coexistence curves for a series of systems. Often bimodal CPCs and shadow curves result, even for systems with a concentration-independent interaction parameter g. The importance of coexistence curves, as opposed to CPCs, for judging the A/B miscibility, recently observed in polydisperse blends, is confirmed in this study. Particular attention is here paid to the critical state. Analytical relations are derived for the critical point (CP) and the critical slopes of the CPC and shadow curve, as well as for the criterion of CP stability, all in terms of various molar-mass averages of A and B. The latter criterion then yields conditions for the existence of heterogeneous double CPs and triple CPs, important as markers announcing the proximity of a three-phase region. Interestingly, the sign of the critical CPC slope depends solely on the relative magnitude of the rz/rw ratios for the two polymers A and B. Hence, a CP located at the CPC's top should not be interpreted as a proof of both polymers' monodispersity. The validity of derived analytical relations is confirmed by numerically computed phase diagrams.

About this research paper

What this paper is about

A method for computing phase diagrams of polydisperse A/B polymer blends is proposed, based on Flory-Huggins-Staverman thermodynamics, and employed to obtain cloud-point curves (CPCs), shadow curves, spinodals and coexistence curves for a series of systems. Often bimodal CPCs and shadow curves result, even for systems with a concentration-independent interaction parameter g. The importance of coexistence curves, as opposed to CPCs, for judging the A/B miscibility, recently observed in polydisperse blends, is confirmed in this study. Particular attention is here paid to the critical state. Analytical relations are derived for the critical point (CP) and the critical slopes of the CPC and shadow curve, as well as for the criterion of CP stability, all in terms of various molar-mass averages of A and B. The latter criterion then yields conditions for the existence of heterogeneous double CPs and triple CPs, important as markers announcing the proximity of a three-phase region. Interestingly, the sign of the critical CPC slope depends solely on the relative magnitude of the rz/rw ratios for the two polymers A and B. Hence, a CP located at the CPC's top should not be interpreted as a proof of both polymers' monodispersity. The validity of derived analytical relations is confirmed by numerically computed phase diagrams.

Why it matters

OpenAlex reports 16 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

A method for computing phase diagrams of polydisperse A/B polymer blends is proposed, based on Flory-Huggins-Staverman thermodynamics, and employed to obtain cloud-point curves (CPCs), shadow curves, spinodals and coexistence curves for a series of systems. Often bimodal CPCs and shadow curves result, even for systems with a concentration-independent interaction parameter g. The importance of coexistence curves, as opposed to CPCs, for judging the A/B miscibility, recently observed in polydisperse blends, is confirmed in this study. Particular attention is here paid to the critical state. Analytical relations are derived for the critical point (CP) and the critical slopes of the CPC and shadow curve, as well as for the criterion of CP stability, all in terms of various molar-mass averages of A and B. The latter criterion then yields conditions for the existence of heterogeneous double CPs and triple CPs, important as markers announcing the proximity of a three-phase region. Interestingly, the sign of the critical CPC slope depends solely on the relative magnitude of the rz/rw ratios for the two polymers A and B. Hence, a CP located at the CPC's top should not be interpreted as a proof of both polymers' monodispersity. The validity of derived analytical relations is confirmed by numerically computed phase diagrams.

Key concepts: Critical point (mathematics), Miscibility, Thermodynamics, Phase diagram, Polymer, Lower critical solution temperature, Binodal, Upper critical solution temperature

Related papers

Back to paper searchBrowse research topicsOriginal source