Introduction of silica into thermo-responsive poly( N-isopropyl acrylamide) hydrogels: A novel approach to improve response rates

Abstract

The response rates of novel thermo-responsive poly( N-isopropyl acrylamide) (PNIPAM) hybrid hydrogels are compared to those of conventional chemically crosslinked PNIPAM hydrogels. The former materials were obtained by applying the sol–gel technology, in which the inorganic silica particles act as physical crosslinks for the organic polymer chains, leading to a semi-interpenetrating polymer network structure. In situ modulated temperature DSC shows that the introduction of hydrophilic silica improves the thermal response rate of the hybrid hydrogels to a great extent as compared to aqueous PNIPAM solutions and conventional PNIPAM hydrogels. Ex situ gravimetrical measurements also illustrate that the shrinking/swelling rate of the hybrid hydrogels is largely improved. It is assumed that the uniform distribution of the SiO 2 units, as demonstrated by cryo-field emission scanning electron microscopy, causes the silica to act as nano-sized water reservoirs, which reduce the characteristic diffusion length of water in the PNIPAM matrix so that it can be transported faster within the hybrid PNIPAM nano-composite.