4.5 Article

Hydration of Cations: A Key to Understanding of Specific Cation Effects on Aggregation Behaviors of PEO-PPO-PEO Triblock Copolymers

Journal

JOURNAL OF PHYSICAL CHEMISTRY B
Volume 117, Issue 35, Pages 10132-10141

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jp405709x

Keywords

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Funding

  1. American Chemical Society [51008-UNI4]
  2. Thomas F. and Kate Miller Jeffress Memorial Trust [J-966]
  3. National Science Foundation [CHE-1062629]

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This work reports results from the interaction's Of a series of monovalent and divalent cations with a triblock copolymer, poly(ethylene oxide)-b-poly(propylene oxide)-b-poly(ethylene oxide)2(PEO-PPO-PEO). Phase transition; temperatures of the polymer in the presence of chloride salts with six monovalent and eight divalent cations Were measured using an automated melting point apparatus The polymer undergoes a two-step Phase consisting of micellization of the polymer followed by aggregation, of the micelles, in the presence of all the salts studied herein. The results suggest that hydration of cations plays a key role in determining the interactions between the cations and the polymer. The modulation of the phase transition temperature, of the polymer by cations Can be explained as a balance between three interactions direct binding of cations to the oxygen in the polymer Chains, cations Sharing one water molecule with the polymer in their hydration layer, and cations interacting with the polymer via two Water molecules Monovalent cations Na+, K+, Rb+, and Cs+ do not bind to the polymer, While Li+ and NH4+ and all the divalent cations investigated including Mg2+, Ca2+, Sr2+, Ba2+, Co2+, Ni2+, Cu2+, and Cd2+ bind to the polymer. The effects of the catkins correlate well with their hydration thermodynamic properties. Mechanisms for Cation polymer interactions are discussed.

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