Abstract
As a thermally sensitive polymer, poly(N-isopropylacrylamide) (PNIPAM) is hydrophilic at temperatures below its lower critical solution temperature (LCST, ∼132°C), but undergoes a coil-to-globule transition in water at higher temperatures. The adsorption of PNIPAM on polystyrene (PS) nanoparticles resulted in a core-shell nanostructure. In the first heating-and-cooling cycle there existed a hysteresis in terms of the thickness of the adsorbed PNIPAM layer; this could be attributed to additional binding of the adsorbed PNIPAM chains to the surface. Moreover, the surface shifted the coil-to-globule transition to a lower temperature and made the transition less sharp. The temperature dependence of the ratio of the radius of gyration to the hydrodynamic radius (<Rg>/<Rh>) revealed that the PNIPAM shell is highly swollen, and the density of the shell in the collapsed state approached that of the PS core.
ACKNOWLEDGMENT
The financial support of the National Distinguished Young Investigator Fund (1996, 29625410), the BASF-Sino-German Research and Development Fund (1998), and the Research Grants Council of Hong Kong Special Administrated Region Earmarked Grant 1997/98 (CUHK4181/97P, 2160082) is gratefully acknowledged.