Gianneli Maria, Roskamp Robert F, Jonas Ulrich, Loppinet Benoit, Fytas George, Knoll Wolfgang
Max Planck Institute for Polymer Research, P. O. Box 3148, Mainz, 55128, Germany and FO.R.T.H/IESL, P. O. Box 1527, 71110 Heraklion, Greece and Department of Materials Science & Technology, University of Crete, Greece.
Max Planck Institute for Polymer Research, P. O. Box 3148, Mainz, 55128, Germany.
Soft Matter. 2008 Jun 20;4(7):1443-1447. doi: 10.1039/b801468j.
We employ a dynamic micro light scattering technique to probe the thermal concentration fluctuations in surface-attached poly-N-isopropylacrylamide (PNIPAAm) gel layers swollen in ethanol as a good solvent. At the equilibrium swelling state, the relaxation function exhibits two decays in the time range between microseconds and seconds and the characteristic rates display a pure diffusive behavior. The fast cooperative diffusion increases with crosslinking density as a result of the decrease in the dynamic network mesh size. This increase is significantly stronger than the concentration dependence of the cooperative diffusion in uncrosslinked linear PNIPPAm solutions. Uniaxial swelling due to the surface attachment and structural inhomogeneities intrinsic to photo-crosslinked gels alter the dynamics of the surface anchored networks compared to the solutions. In contrast to the frozen inhomogeneities in conventional gels, the slow diffusion in the present anchored layers was found to be ergodic. It might relate to structural inhomogeneities but its nature is not clarified yet.
我们采用动态微光散射技术来探测在作为良溶剂的乙醇中溶胀的表面附着的聚-N-异丙基丙烯酰胺(PNIPAAm)凝胶层中的热浓度涨落。在平衡溶胀状态下,弛豫函数在微秒到秒的时间范围内呈现出两种衰减,且特征速率表现出纯扩散行为。由于动态网络网眼尺寸减小,快速协同扩散随交联密度增加。这种增加比未交联的线性PNIPPAm溶液中协同扩散的浓度依赖性显著更强。与溶液相比,由于表面附着和光交联凝胶固有的结构不均匀性导致的单轴溶胀改变了表面锚定网络的动力学。与传统凝胶中固定的不均匀性不同,发现当前锚定层中的缓慢扩散是遍历性的。它可能与结构不均匀性有关,但其本质尚未阐明。