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Equilibrium Structure of Hydrogen-Bonded Polymer Blends

Published

Author(s)

C Zhou, Erik K. Hobbie, Barry J. Bauer, Charles C. Han

Abstract

Deuterium-labeled polystyrene modified by random distributions of the comonomer p-(1,1,1,3,3,3-hexaflouro-2-hydroxyisopropyl)-α-Methyl-styrene [DPS(OH)] has been blended with poly (butyl methacrylate) (PBMA) and studied with small-angle neutron scattering (SANS). Miscibility is induced via hydrogen bonding between the DPS (OH) hydroxyl group and PBMA carbonyl groups. The data suggest that the nature of the miscible-phase structure in these blends differs from that of the usual homopolymer blends at small scattering angles, which we attribute to the short-range site specific nature of the hydrogen bond interaction.
Citation
Journal of Polymer Science Part B-Polymer Physics
Volume
36
Issue
No. 15

Keywords

hydrogen bond, polymer blend, SANS

Citation

Zhou, C. , Hobbie, E. , Bauer, B. and Han, C. (1998), Equilibrium Structure of Hydrogen-Bonded Polymer Blends, Journal of Polymer Science Part B-Polymer Physics, [online], https://tsapps.nist.gov/publication/get_pdf.cfm?pub_id=851437 (Accessed April 14, 2024)
Created November 1, 1998, Updated February 17, 2017