Dynamics of thermoresponsive PNIPAM- g-PEO copolymer chains in semi-dilute solution

Abstract

The effects of concentration and temperature on dynamics of poly( N-isopropylacrylamide)- graft-poly(ethylene oxide) (PNIPAM- g-PEO) chains in semi-dilute aqueous solution were studied by static and dynamic laser light scattering. The intensity–intensity time correlation function shows a fast and a slow relaxation mode, with line widths Γ f and Γ s, respectively. Γ f is scaled to the scattering vector ( q) as Γ f ∝ q 2, revealing that it is due to the cooperative diffusion of the subchains between two neighboring entangled points. As the concentration increases, the slow relaxation becomes slower and contributes more to the total scattered light intensity, indicating that the slow relaxation is related to the chain entanglement. On the other hand, when the solution temperature increases, the PNIPAM chain backbone shrinks, but the fast relaxation remains and the slow mode slows down with a minimum rate at ∼33 °C. It indicates that the slow mode arises from inter-chain clustering, which is gradually suppressed by the intra-chain shrinking. The sample position independence of the time-averaged scattered light intensity 〈 I〉 T reveals that the solution is homogeneous and the clustering is transient.