brief report is given of the method of intermittent illumination and of the rotating sector polymerization instrument built in our laboratory. The solvent dependence of chain propagation and termination rate constants was investigated for the polymerization system styrene-benzene at 50. The observed
Investigation of the Peak Width of Polystyrene Prepared by Rotating-Sector Polymerization in Microemulsion
✍ Scribed by Irene Schnöll-Bitai; Christian Pfeisinger
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 156 KB
- Volume
- 204
- Category
- Article
- ISSN
- 1022-1352
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Styrene was polymerized by intermittent photoinitiation (at a constant sector speed and a light to dark ratio of 1:5) in microemulsion. The molecular weight distribution was measured by size‐exclusion chromatography and turned out to be extremely well structured. When the points of inflection were used for the calculation of the rate constant of propagation in analogy to pulsed‐laser polymerization/size‐exclusion chromatography (PLP‐SEC), values were obtained which were lower than those accepted for bulk polymerization but good agreement was achieved with a slightly modified equation. The absolute peak width (introduced as the difference between two successive points of inflection) turned out to be an invariant quantity no matter which type of distribution curve (number, molar mass, or hyper distribution) was analyzed, thus demonstrating the Poissonian character of the peaks. Furthermore, the relative peak widths (defined as the ratio of two successive points of inflection) for the first peak scattered between 1.35–1.45, those for the second peak between 1.26–1.30. After subtracting the respective value for the theoretical peak width, the same value for the first and second peaks was obtained for all experiments over a broad range of experimental parameters. As the appearing peaks are well resolved and narrow, the influence of axial dispersion on the results is, therefore, conclusively demonstrated. A simple procedure for the direct determination of axial dispersion is presented based on the relative peak widths and the additivity of the peak variances. The invariance of the peak widths is an easily verifiable theoretical and experimental prerequisite for this procedure.
Comparison of GPC traces of a microemulsion polymerization of styrene (t~0~ = 1.4 s, [M] = 4.326 mol · l^−1^; light‐to‐dark ratio 1:5; full line) and of a standard mixture (styrene, peak masses: 1 950, 89 400, 993 000; dashed line).
imageComparison of GPC traces of a microemulsion polymerization of styrene (t~0~ = 1.4 s, [M] = 4.326 mol · l^−1^; light‐to‐dark ratio 1:5; full line) and of a standard mixture (styrene, peak masses: 1 950, 89 400, 993 000; dashed line).
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