30 research outputs found
Correlation between Cohesive Energy Density, Fractional Free Volume, and Gas Transport Properties of Poly(ethylene-co-vinyl acetate) Materials
The transport properties of the poly(ethylene-co-vinyl acetate) (EVA) materials to He, N2, O2, and CO2 are correlated with two polymer molecular structure parameters, that is, cohesive energy density (CED) and fractional free volume (FFV), determined by the group contribution method. In our preceding paper, the attempt was made to approximate EVA permeability using a linear function of 1/FFV as predicted by the free volume theory. However, the deviations from this relationship appeared to be significant. In this paper, it is shown that permeation of gas molecules is controlled not only by free volume but also by the polymer cohesive energy. Moreover, the behavior of CO2 was found to differ significantly from that of other gases. In this instance, the correlation is much better when diffusivity instead of permeability is taken into account in a modified transport model
Relationship between structure and aromatic solvent permeability of crosslinked polyurethanes based on hyperbranched polyesters
Synthesis and characterization of a novel kind of thermotropic liquid crystalline poly(urea-ester)s based on bis(4?-hydroxyphenyl)-tolyene-2,4-diurea
Physico-chemical properties of new composite polymer for heat resistance with thin-film form through the blending of m-aramid and polyurethane (PU)
MoDeNa Nanotools: An integrated multiscale simulation workflow to predict thermophysical properties of thermoplastic polyurethanes
Poly(urethane鈥搖rea) based on functionalized polystyrene with HMDI: Synthesis and characterization
Spacer length controlled highly thermo reversible polyurethane-urea based on polystyrene: synthesis and crystallization studies
Hydroxyl-terminated poly(urethane acrylate) as a soft liner in dental applications: Synthesis and characterization
Hydroxyl-terminated poly(urethane acrylate)s were synthesized for use in biomedical applications. Acrylate end capping via an interesterification reaction was successfully achieved with methacryloyl chloride addition to the hydroxyl ends of the polyurethane at low temperatures. 2,4-Toluene diisocyanate, 1,6-hexane diisocyanate, and methylene diphenyl diisocyanate were used as diisocyanates for urethane synthesis, and they were end-capped with methyl methacrylate and hydroxyethyl methacrylate. The nature of the monomers that we used had an effect on the thermal and morphological properties that were interpreted in terms of the level of hydrogen bonding and the degree of phase separation. The synthesized polymers were characterized by NMR, Fourier transform infrared/attenuated total reflectance spectroscopy, differential scanning calorimetry, thermogravimetric analysis, and gel permeation chromatography. The number-average molecular weights of the poly(urethane acrylate)s were 2500-6000 g/mol. To use the polymer as a soft-liner material in denture applications, the residual isocyanate should not exist. In this study, we showed that a prepolymer without residual isocyanate could be synthesized. (C) 2010 Wiley Periodicals, Inc. J Appl Polym Sci 117: 458-466, 201