Competitive calcium ion binding to end-tethered weak polyelectrolytes

被引:41
作者
Nap, Rikkert J.
Park, Sung Hyun
Szleifer, Igal [1 ]
机构
[1] Northwestern Univ, Dept Chem, Dept Biomed Engn, Evanston, IL 60208 USA
关键词
IRON-OXIDE NANOPARTICLES; POLY(ACRYLIC ACID) BRUSHES; GRAFTING DENSITY GRADIENTS; FLEXIBLE POLYELECTROLYTES; COUNTERION-CONDENSATION; POLYACRYLIC-ACID; POLYMER BRUSHES; COLLAPSE; BEHAVIOR; CHAINS;
D O I
10.1039/c7sm02434g
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We have developed a molecular model to describe the structural changes and potential collapse of weak polyelectrolyte layers end-tethered to planar surfaces and spherical nanoparticles as a function of pH and divalent ion concentration. In particular, we describe the structural changes of polymer-coated nanoparticles end-tethered to copolymers of poly(acrylic acid) (pAA) and poly arcrylamido-2-methylpropane sulfonate (pAMPS) in the presence of Ca2+ ions. We find that end-grafted poly(acrylic acid) layers will collapse in aqueous solutions containing sufficient amounts of Ca2+ ions, while polymers and copolymers with sufficient AMPS monomers will not collapse. The collapse of end-tethered pAA is due to the formation of calcium bridges between two acrylic acid monomers and one calcium ion. On the other hand pAMPS layers do not collapse due to the lack of calcium bridges. The collapse of pAA layers is strongly dependent on the pH as well as divalent and monovalent salt concentrations of the environment. The collapse is also strongly influenced by the curvature of the tethering surface.
引用
收藏
页码:2365 / 2378
页数:14
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