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Effect of Polydispersity on the Phase Behavior of Polymer Blends

✍ Scribed by Chieh-Tsung Lo; Soenke Seifert; Pappannan Thiyagarajan; Balaji Narasimhan


Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
144 KB
Volume
26
Category
Article
ISSN
1022-1336

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✦ Synopsis


Abstract

Summary: The effect of polydispersity on polymer blend phase behavior is studied by in situ small‐angle X‐ray scattering. In a polydisperse polyethylene (PE)/isotactic poly(propylene) (iPP) blend, the enthalpic portion of the interaction parameter is greater than that of a corresponding blend with lower polydispersity. This is attributed to the presence of long chains, which provide a higher interaction energy and packing constraint, reducing the system miscibility. As expected, the radius of gyration is higher in the system with higher polydispersity.

Comparison of phase diagrams of the iPP/PE system used in this study (thin lines) with that obtained from the literature (thick lines). The solid lines represent binodals and the dashed lines are spinodals.

imageComparison of phase diagrams of the iPP/PE system used in this study (thin lines) with that obtained from the literature (thick lines). The solid lines represent binodals and the dashed lines are spinodals.


πŸ“œ SIMILAR VOLUMES


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The changes in molecular mass distribution (MMD) after adsorption from solution in concentration regions below and above the critical concentration of overlapping have been studied for various polymers and their mixtures. It was found that the formation of entanglements in both binary and ternary so

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## Abstract **Summary:** The chain‐length dependence of the Flory‐Huggins (FH) interaction parameter is introduced into the FH lattice theory for polydisperse polymer‐blend systems. The spinodals are calculated for the model polymer blends with different chain lengths and distributions. It is found