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000038826 084__ $$2WoS$$aPhysics, Atomic, Molecular & Chemical
000038826 1001_ $$0P:(DE-HGF)0$$aKita, R.$$b0
000038826 245__ $$aSign change of the Soret coefficient of poly(ethylene oxide) in water/ethanol mixtures observed by thermal diffusion forced Rayleigh scattering
000038826 260__ $$aMelville, NY$$bAmerican Institute of Physics$$c2004
000038826 300__ $$a3874 - 3885
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000038826 440_0 $$03145$$aJournal of Chemical Physics$$v121$$x0021-9606$$y8
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000038826 520__ $$aSoret coefficients of the ternary system of poly(ethylene oxide) in mixed water/ethanol solvent were measured over a wide solvent composition range by means of thermal diffusion forced Rayleigh scattering. The Soret coefficient S(T) of the polymer was found to change sign as the water content of the solvent increases with the sign change taking place at a water mass fraction of 0.83 at a temperature of 22 degrees C. For high water concentrations, the value of S(T) of poly(ethylene oxide) is positive, i.e., the polymer migrates to the cooler regions of the fluid, as is typical for polymers in good solvents. For low water content, on the other hand, the Soret coefficient of the polymer is negative, i.e., the polymer migrates to the warmer regions of the fluid. Measurements for two different polymer concentrations showed a larger magnitude of the Soret coefficient for the smaller polymer concentration. The temperature dependence of the Soret coefficient was investigated for water-rich polymer solutions and revealed a sign change from negative to positive as the temperature is increased. Thermodiffusion experiments were also performed on the binary mixture water/ethanol. For the binary mixtures, the Soret coefficient of water was observed to change sign at a water mass fraction of 0.71. This is in agreement with experimental results from the literature. Our results show that specific interactions (hydrogen bonds) between solvent molecules and between polymer and solvent molecules play an important role in thermodiffusion for this system.
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000038826 7001_ $$0P:(DE-Juel1)131034$$aWiegand, S.$$b1$$uFZJ
000038826 7001_ $$0P:(DE-HGF)0$$aLuettmer-Strathmann, J.$$b2
000038826 773__ $$0PERI:(DE-600)1473050-9$$a10.1063/1.1771631$$gVol. 121, p. 3874 - 3885$$p3874 - 3885$$q121<3874 - 3885$$tThe @journal of chemical physics$$v121$$x0021-9606$$y2004
000038826 8567_ $$uhttp://hdl.handle.net/2128/1187$$uhttp://dx.doi.org/10.1063/1.1771631
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