Department of Polymer Science and Engineering, University of Massachusetts, Amherst, Massachusetts 01003, USA.
J Chem Phys. 2010 Feb 28;132(8):084901. doi: 10.1063/1.3328821.
Theoretical investigations of phase separation in polyelectrolyte solutions have so far assumed that the effective charge of the polyelectrolyte chains is fixed. The ability of the polyelectrolyte chains to self-regulate their effective charge due to the self-consistent coupling between ionization equilibrium and polymer conformations, depending on the dielectric constant, temperature, and polymer concentration, affects the critical phenomena and phase transitions drastically. By considering salt-free polyelectrolyte solutions, we show that the daughter phases have different polymer charges from that of the mother phase. The critical point is also altered significantly by the charge self-regularization of the polymer chains. This work extends the progress made so far in the theory of phase separation of strong polyelectrolyte solutions to a higher level of understanding by considering chains which can self-regulate their charge.
到目前为止,关于聚电解质溶液相分离的理论研究假设聚电解质链的有效电荷是固定的。由于离子平衡和聚合物构象之间的自洽耦合,聚电解质链能够根据介电常数、温度和聚合物浓度自我调节其有效电荷,这会剧烈影响临界现象和相转变。通过考虑无盐的聚电解质溶液,我们表明子相具有与母相不同的聚合物电荷。聚合物链的电荷自调节也会显著改变临界点。这项工作通过考虑可以自我调节电荷的链,将强聚电解质溶液相分离理论的进展提高到了更高的理解水平。