Thermal Diffusion Behavior of Nonionic Surfactants in Water

Ning, H.; Kriegs, H.; Luettmer-Strathmann, J.; Kita, R.; Wiegand, S.

doi:10.1021/jp0572986

Journal Article

PreJuSER-51504

Thermal Diffusion Behavior of Nonionic Surfactants in Water

Ning, H.FZJ* ; Kita, R. ; Kriegs, H.FZJ* ; Luettmer-Strathmann, J. ; Wiegand, S.FZJ*

2006
Soc. Washington, DC

The journal of physical chemistry <Washington, DC> / B 110, 10746 (2006) [10.1021/jp0572986]

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Please use a persistent id in citations: http://hdl.handle.net/2128/1205 doi:10.1021/jp0572986

Abstract: We studied the thermal diffusion behavior of hexaethylene glycol monododecyl ether (C12E6) in water by means of thermal diffusion forced Rayleigh scattering (TDFRS) and determined Soret coefficients, thermal diffusion coefficients, and diffusion constants at different temperatures and concentrations. At low surfactant concentrations, the measured Soret coefficient is positive, which implies that surfactant micelles move toward the cold region in a temperature gradient. For C12E6/water at a high surfactant concentration of w1 = 90 wt % and a temperature of T = 25 degrees C, however, a negative Soret coefficient S(T) was observed. Because the concentration part of the TDFRS diffraction signal for binary systems is expected to consist of a single mode, we were surprised to find a second, slow mode for C12E6/water system in a certain temperature and concentration range. To clarify the origin of this second mode, we investigated also, tetraethylene glycol monohexyl ether (C6E4), tetraethylene glycol monooctyl ether (C8E4), pentaethylene glycol monododecyl ether (C12E5), and octaethylene glycol monohexadecyl ether (C16E8) and compared the results with the previous results for octaethylene glycol monodecyl ether (C10E8). Except for C6E4 and C10E8, a second slow mode was observed in all systems usually for state points close to the phase boundary. The diffusion coefficient and Soret coefficient derived from the fast mode can be identified as the typical mutual diffusion and Soret coefficients of the micellar solutions and compare well with the independently determined diffusion coefficients in a dynamic light scattering experiment. Experiments with added salt show that the slow mode is suppressed by the addition of w(NaCl) = 0.02 mol/L sodium chloride. This suggests that the slow mode is related to the small amount of absorbing ionic dye, less than 10(-5) by weight, which is added in TDFRS experiments to create a temperature grating. The origin of the slow mode of the TDFRS signal will be tentatively interpreted in terms of a ternary mixture of neutral micelles, dye-charged micelles, and water.

Keyword(s): Diffusion (MeSH) ; Surface-Active Agents: chemistry (MeSH) ; Temperature (MeSH) ; Water: chemistry (MeSH) ; Surface-Active Agents ; Water ; J