Dupin Damien, Rosselgong Julien, Armes Steven P, Routh Alexander F
Department of Chemistry, Dainton Building, The University of Sheffield, Brook Hill, Sheffield, South Yorkshire, S3 7HF United Kingdom.
Langmuir. 2007 Mar 27;23(7):4035-41. doi: 10.1021/la063278z. Epub 2007 Feb 22.
The kinetics of swelling of a series of six near-monodisperse, lightly cross-linked poly(2-vinylpyridine) latexes with mean diameters ranging from 380 to 1010 nm has been investigated by the pH jump method using a commercial stopped-flow instrument. These pH-responsive particles become substantially protonated at around pH 4.1, which leads to a rapid latex-to-microgel transition within a time scale of tens of milliseconds. The characteristic swelling time correlates linearly with the mean particle diameter, as predicted by the Tanaka equation. However, faster swelling is observed in the presence of added salt. This is contrary to the theory developed by Tanaka, which assumes that the relaxation of the polymer chains is the rate-limiting step. An alternative viewpoint, in which infusion of solvent determines the characteristic swelling time, satisfactorily explains the experimental observations and collapses most of the data, except for the largest microgels. This discrepancy is suggested to be due to the inaccurate sizing of these micrometer-sized swollen microgels by dynamic light scattering.
使用商用停流仪器,通过pH跃变法研究了一系列六种平均直径在380至1010纳米之间的近单分散、轻度交联的聚(2-乙烯基吡啶)胶乳的溶胀动力学。这些对pH有响应的颗粒在pH约4.1时基本上会质子化,这会导致在几十毫秒的时间尺度内从胶乳快速转变为微凝胶。如田中方程所预测的,特征溶胀时间与平均粒径呈线性相关。然而,在添加盐的情况下观察到溶胀更快。这与田中提出的理论相反,该理论假设聚合物链的松弛是限速步骤。另一种观点认为溶剂的注入决定了特征溶胀时间,这令人满意地解释了实验观察结果,并使大部分数据符合规律,除了最大的微凝胶。这种差异被认为是由于通过动态光散射对这些微米级溶胀微凝胶的尺寸测量不准确所致。