Amphiphilic networks. XI. Mechanical properties and morphology

• Published in: Journal of applied polymer science Vol. 66; no. 5; pp. 901 - 910
• Main Authors: Park, Dongkyu, Keszler, Balazs, Galiatsatos, Vassilios, Kennedy, Joseph P.
• Format: Journal Article
• Language: English
• Published: New York John Wiley & Sons, Inc 31.10.1997; Wiley
• Subjects: amphiphilic networks; Applied sciences; Exact sciences and technology; mechanical properties; morphology; Organic polymers; Physicochemistry of polymers; Properties and characterization; Solution and gel properties; transition; Colloidal gel; Dynamic mechanical properties; Property composition relationship; Supramolecular structure; Isobutene copolymer; Mechanical properties; Acrylamide derivative copolymer; Hydroxyethyl methacrylate copolymer; Small angle X ray scattering; Experimental study; Thermal stability; Amphiphilic polymer
• ISSN: 0021-8995; 1097-4628
• DOI: 10.1002/(SICI)1097-4628(19971031)66:5<901::AID-APP10>3.0.CO;2-Q

The bulk properties of two types of amphiphilic networks, poly(2‐hydroxyethyl methacrylate)‐l‐polyisobutylene (PHEMA‐l‐PIB, H‐network) and poly(N,N‐dimethylacrylamide)‐l‐polyisobutylene (PDMAAm‐l‐PIB, A‐network), have been investigated. Tensile strengths decreased considerably by swelling, and the decrease was more severe by swelling in water than in n‐heptane. Elongations increased by swelling in water; however, the change was not consistent upon swelling in n‐heptane. The hardness of dry networks decreased with increasing PIB content, while for wet networks it was similar to dry networks containing 85 wt % PIB. Small‐angle X‐ray scattering showed that average interdomain spacings decreased with increasing PIB content. According to dynamic mechanical thermal analysis (DMTA) the glass transition temperatures (Tg) of the respective hydrophobic and hydrophilic components shift toward each other with increasing PIB content. A “liquid‐liquid transition” (Tll) above the Tg of the hydrophilic component was apparent by DMTA, but could not be found by differential scanning calorimetry (DSC). © 1997 John Wiley & Sons, Inc. J Appl Polym Sci 66: 901–910, 1997