Mixed polymer hydrogel

Other novel mixed polymer systems have included glycosaminoglycans (GAGs) modified with multiblock copolymers to form self-assembling, crosslinker free hydrogels. For example, aminooxy pluronic derivatives were coupled with HA to give amphiphilic hydrogels with the ability to bind to hydrophobic surfaces (89). 

Conducting polymers can be mixed with or electrochemically deposited onto transition metal oxides to achieve better performances as electrode materials. However, the wrapping of conducting polymers on metal oxides may reduce the effective contact area between metal oxides and electrolytes. This will further impede insertion of alkali ions into metal oxides and result in poor rate performance with low specific capacitance. A rational strategy is to use conducting polymers as active electrode materials directly and optimize their structures. To this end, a hierarchically nanostructured conductive polymer hydrogel was synthesized by a facile interfacial polymerization (Shi et al., 2014). 

Polymer complexes associated with two or more complementary polymers are widely used in potential applications in the form of particles, hydrogels, films, and membranes. In particular, a polyion complex (PIC) can be easily formed when oppositely charged polyelectrolytes are mixed in aqueous solution and interact via... 

The structure of hydrogels that do not contain ionic moieties can be analyzed by the Flory Rehner theory (Flory and Rehner 1943a). This combination of thermodynamic and elasticity theories states that a cross-linked polymer gel which is immersed in a fluid and allowed to reach equilibrium with its surroundings is subject only to two opposing forces, the thermodynamic force of mixing and the retractive force of the polymer chains. At equilibrium, these two forces are equal. Equation (1) describes the physical situation in terms of the Gibbs free energy. 

It must be noted that Eqs. (35) and (36) are for the case in which the crosslinks in the polymer network were introduced in solution as with the Peppas-Merrill equation for neutral hydrogels and also that a Gaussian chain distribution is assumed. The complete equilibrium expressions accounting for the mixing, elastic-retractive, and ionic contributions to the chemical potential for anionic networks in the two cases described above are then... 

The principal polyphosphazenes that have been used in hydrogels are those with linear or branched ethyleneoxy side chains, aryloxy groups with carboxylic acid substituents, or mixed-substituent polymers that bear hydrophilic methylamino side groups plus a hydrophobic cosubstituent such as phenoxy or trifluoroethoxy. Cross-linking is usually accomplished by gamma-ray irradiation or, in the case of the carboxylic acid functional species, by treatment with a di- or tri-valent cation. Here, we will consider another example based on MEEP (3.79), a polymer that is well suited to the clean method of radiation cross-linking. 

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