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(organic chemistry)
A natural or synthetic electrolyte with high molecular weight, such as proteins, polysaccharides, and alkyl addition products of polyvinyl pyridine; can be a weak or strong electrolyte; when dissociated in solution, it does not give uniform distribution of positive and negative ions (the ions of one sign are bound to the polymer chain while the ions of the other sign diffuse through the solution).



a polymer electrolyte, that is, a polymer that dissociates into ions in solution. A large number of periodically repeating charges arises in each macromolecule during dissociation. Polyelectrolytes are divided into polyacids (for example, polyacrylic acids), polybases (such as polyvinyl pyridinium), and polyampholytes (copolymers containing both basic and acidic groups). Most polyelectrolytes contain weak acidic or basic groups and therefore are ionized only in the presence of a strong base (for a polyacid) or strong acid (for a polybase).

Primary biopolymers such as proteins and nucleic acids are among the polyelectrolytes. Cross-linked polyelectrolytes, which are prepared by the introduction of readily dissociating groups (for example, sulfo and amino groups) into various cross-linked polymers, are of great importance to industry and laboratory practice. The most valuable cross-linked polyelectrolytes are ion-exchange resins.

The dissociating groups in the polymer molecules determine the solubility of polyelectrolytes in water and other polar liquids. For example, a sulfonated linear polystyrene dissolves freely in water, although polystyrene itself is one of the most water-resistant polymers known. Cross-linked polyelectrolytes of three-dimensional structure swell in water rather than dissolving. The properties of polyelectrolyte molecules in solution are determined by the electrostatic interaction of charged groups in the chain with one another and with low-molecular-weight ions in the solution. The strong electrostatic field generated by the charges in the polyelectrolyte molecule holds a large number of oppositely charged ions close to the molecule. The electrostatic repulsion of groups of like charge leads to a substantial alteration of the macromolecular conformations in solutions: the effective size of the molecules increases, and the coiled chains straighten out, assuming an approximately linear form as the degree of polyelectrolyte dissociation increases. The physicochemical properties of solutions also undergo considerable alteration (for example, solution viscosity increases by hundreds and thousands; the higher the concentration, the greater the viscosity). The theory that was developed for solutions of low-molecular-weight electrolytes ceases to be valid for polyelectrolyte solutions. The low-molecular-weight ions that appear during the dissociation of polar groups of these polyelectrolytes create a diffuse shell around the oppositely charged surface of the polymer and may to some degree be replaced by other ions of like sign.


Tager, A. A. Fiziko-khimiia polimerov, 2nd ed. Moscow, 1968.
Rice, S. A., and M. Nagasawa. Polyelectrolyte Solutions: A Theoretical Introduction. London-New York, 1961.


References in periodicals archive ?
Besides its appealing simplicity, the LbL assembly is regarded as an extremely versatile bottom-up nanofabrication technique, since it allows the construction of PEMs films that have a great variety of architectures, by changing the types of polyelectrolyte components, the number of layers, and the layering sequence.
will have the tendency to form ion pairs by interlayer diffusion or interpenetration [37], making the polyelectrolyte layer may not have the perfect layer-by-layer structures.
This suggests two possible mechanisms by which the system would pick the antigen: firstly by entrapment into the hollow core of the nanoparticle or secondly, by adsorption unto the peripheral PSS layer which can be tuned to multilayered assembly system using LBL polyelectrolyte approach to decorate the resulting system with other immune boosters (UA and IL-12) for a longer-lasting immune recognition (Fig.
One alternative that can address the issue of electrode stability and longevity is to use polyelectrolyte multilayer (PEM) coatings.
Lipid coating on polyelectrolyte surface modified colloidal particles and polyelectrolyte capsules.
Counterion induced bundle formation of rodlike polyelectrolytes.
Quartz Crystal Resonator as a Tool for Following the Buildup of Polyelectrolyte Multilayers
In recent years, polyelectrolytes have been extensively studied experimentally, theoretically, and computationally as most biopolymers are polyelectrolytes (or polyampholytes) and they play very important roles in diverse industries.
Lahann and Kazemi have prepared multiphase nano- to micro-particles such as core-shell or anisotropic (Janus) multiphase particles with well-defined structures using electrohydrodynamic co-jetting of two different polyelectrolyte solutions.
Two tenders for the supply of (a) 13 tons polymer (positive charged polyelectrolyte compounds + cation) required for the hardening of sludge emitted during potable water treatment at Al Marj potable water treatment plant and (b) lube oils for the Automotive Dept.
APPLICATION: This equation will help analysts determine the surface charge of pulp fibers from polyelectrolyte adsorption data.
University of Akron, Deparment of Polymer Engineering, seminar on "New understanding and application of layer-by-layer polyelectrolyte assembly," Polymer Engineering Academic Center, Akron, OH, Thein Kyu (330) 972-6672--October 29.