This article presents thermal diffusivity (D) measurement by flash radiometry for the polymer blend of polycaprolactone (PCL) and poly(bisphenol A carbonate) (PC) with a lower critical solution temperature (LCST) phase diagram. The dependence of D on temperature is significantly changed by annealing
Thermal diffusivity study of polystyrene/poly(vinyl methyl ether) blends by flash radiometry
β Scribed by Naoto Tsutsumi; Shigenobu Kizu; Wataru Sakai; Tsuyoshi Kiyotsukuri
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 235 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0887-6266
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β¦ Synopsis
This article presents thermal diffusivity ( D) measurements by flash radiometry for the polymer blend of polystyrene (PS) and poly(vinyl methyl ether) (PVME) with lower critical solution temperature (LCST) phase diagram. Dependence of D on PS content measured at 100ΠC coincides a phase diagram determined by a cloud point measurement. D value for the blend decreases with increasing PS content and has minimum value at the PS content around 20 wt % from which D increases again with increasing PS content. If the concentration fluctuation between two components in the miscible states at the temperature close to LCST causes the remarkable phonon scattering, the composition dependence of D would resemble the phase diagram. D for the sample in the phase-separated state is larger than that for the miscible state. The larger D in the phase-separated sample would be due to the decrease of the total surface area microscopically contacted to the counter component in the phase-separated state. Dependence of D on temperature for the phase-separated sample is quite different from that of the miscible one. On an isothermal measurement of D for PS/PVME (10 : 90) at 110ΠC just below the cloud point, D started to increase at time above 100 min and leveled out above 250 min. Isothermal observation of sample film by a differential interference contrast microscopy showed the creation of some structure due to the nucleation and growth of interface at 225 min and it became obvious above 250 min. Thus, the increase in D at 110ΠC implies that D can sensitively reflect the change in microscopic structures which follows the nucleation and growth of interface.
π SIMILAR VOLUMES
Polystyrene (PS) samples carrying terminal or in-chain nitroxide spin labels have been blended with poly(vinyl methyl ether) (PVME) in varying proportions and their electron spin resonance (ESR) spectra recorded over a range of temperatures. The spectra are mainly of the slow-motion type but reΓect
A series of blends of poly(vinyl chloride) (PVC) with ( 1) poly(methyl methacrylate) (PMMA) or ( 2) polyoxymethylene (POM), with lithium acetate as a stabilizing agent, was investigated by differential scanning calorimetry (DSC), scanning electron microscopy (SEM), and thermogravimetric analysis (TG