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Synthesis of Cyclic Polymers and Characterization of Their Diffusive Motion in the Melt State at the Single Molecule Level
Published on: September 26, 2016
Kinetics of chain collapse in dilute polymer solutions: molecular weight and solvent dependences
Yasuyuki Maki1, Toshiaki Dobashi, Mitsuo Nakata
1Department of Biological and Chemical Engineering, Faculty of Engineering, Gunma University, Kiryu 376-8515, Japan.
Abstract:
The molecular weight and solvent dependences of the characteristic time of chain collapse were studied for poly(methyl methacrylate) (PMMA) of the molecular weight Mw=6.4x10(6) and 1.14x10(7) in pure acetonitrile (AcN) and in the mixed solvent of AcN+water (10 vol %). The size of PMMA chains was measured as a function of the time after the quench by static light scattering and the chain collapse processes were expressed by the plot of the expansion factor alpha2 vs ln t. The chain collapse in the mixed solvent AcN+water (10 vol %) was found to occur much faster than that in pure AcN, though the measurement of the former collapse process required several hours. In order to make a comparison between the rates of chain collapses, the fast chain collapse process was superposed on the slow one by scaling the time of the fast process as gammat. The scale factor gamma was determined by comparing the chain collapse processes of nearly the same equilibrium expansion factor with each other. Accordingly, the superposition of the collapse for Mw=6.4x10(6) on that for Mw=1.14x10(7) yielded gammam=4.0+/-0.6 for the process in AcN+water and 5.5+/-0.6 in AcN. The superposition of the chain collapse process in AcN+water on that in AcN yielded gammas=9.5+/-1.4 for Mw=6.4x10(6) and 12.0+/-1.8 for Mw=1.14x10(7). This analysis suggests that gammam and gammas are constant independent of each other. Thus, by assuming the molecular weight dependence of gammam approximately Mz, the characteristic time tauexp of chain collapse was conjectured as tauexp approximately kappaMz, where kappa reflects the nature of solvent species. The ratio of kappa for PMMA in AcN to that in AcN+water is given by gammas. The exponent was estimated to be z=2.4+/-0.7 for AcN+water and 3.0+/-0.7 for AcN. These values are compatible with the theoretical prediction z=3 based on a phenomenological model, though the observed characteristic times are longer by several orders of magnitude than those of the theoretical prediction.
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