Thermophoresis is the rectification of Brownian motion induced by the presence of a thermal gradient ∇T, yielding a net drift of colloidal particles along or against the direction of ∇T. The effect is known to depend on the specific interactions between solute and solvent, and quantitative theoretical models are lacking except in a few simple experimental cases. Both the order of magnitude and the temperature dependence of the thermophoretic mobility DT are known to be very similar for a wide class of aqueous colloidal systems, ranging from latex colloids to polymers, surfactant micelles, proteins, and DNA. Here we show that thermoresponsive microgel particles made of poly(N-isopropylacrylamide) (PNIPAM) do not share, in the temperature range around the ϑ-point, these common features. Instead, DT displays an unusually strong temperature dependence, maintaining a linear growth across the collapse transition. This behaviour is not shared by linear PNIPAM chains, for which existing data show DT falling at the transition, with similar values between the expanded coil and collapsed globule states away from the transition point. A possible connection of the observed giant temperature dependence of DT to microgel hydration is suggested.
Giant thermophoresis of poly(N-isopropylacrylamide) microgel particles / S. Wongsuwarn, D. Vigolo, R. Cerbino, A. M. Howe, A. Vailati, R. Piazza, P. Cicuta. - In: SOFT MATTER. - ISSN 1744-683X. - 8:21(2012 Apr 23), pp. 5857-5863.
|Titolo:||Giant thermophoresis of poly(N-isopropylacrylamide) microgel particles|
|Parole Chiave:||thermophoresis ; soret effect ; optical techniques ; microgel|
|Settore Scientifico Disciplinare:||Settore FIS/07 - Fisica Applicata(Beni Culturali, Ambientali, Biol.e Medicin)|
Settore FIS/03 - Fisica della Materia
|Data di pubblicazione:||23-apr-2012|
|Digital Object Identifier (DOI):||http://dx.doi.org/10.1039/c2sm25061f|
|Appare nelle tipologie:||01 - Articolo su periodico|