TL;DR: In this article, double-network gels are characterized by a special network structure consisting of two types of polymer components with opposite physical natures: the minor component is abundantly crosslinked polyelectrolytes (rigid skeleton) and the major component comprises of poorly cross-linked neutral polymers (ductile substance).
Abstract: Double-network (DN) gels have drawn much attention as an innovative material having both high water content (ca. 90 wt%) and high mechanical strength and toughness. DN gels are characterized by a special network structure consisting of two types of polymer components with opposite physical natures: the minor component is abundantly cross-linked polyelectrolytes (rigid skeleton) and the major component comprises of poorly cross-linked neutral polymers (ductile substance). The former and the latter components are referred to as the first network and the second network, respectively, since the synthesis should be done in this order to realize high mechanical strength. For DN gels synthesized under suitable conditions (choice of polymers, feed compositions, atmosphere for reaction, etc.), they possess hardness (elastic modulus of 0.1–1.0 MPa), strength (failure tensile nominal stress 1–10 MPa, strain 1000–2000%; failure compressive nominal stress 20–60 MPa, strain 90–95%), and toughness (tearing fracture energy of 100∼1000 J m−2). These excellent mechanical performances are comparable to that of rubbers and soft load-bearing bio-tissues. The mechanical behaviors of DN gels are inconsistent with general mechanisms that enhance the toughness of soft polymeric materials. Thus, DN gels present an interesting and challenging problem in polymer mechanics. Extensive experimental and theoretical studies have shown that the toughening of DN gel is based on a local yielding mechanism, which has some common features with other brittle and ductile nano-composite materials, such as bones and dentins.
TL;DR: Possible areas of application for polyelectrolyte shells range from the pharmaceutical, food, cosmetic, and paint industries to catalysis and microcrystallization.
Abstract: Exact control of the film thickness of polyelectrolyte shells (a transmission electron microscopy image is shown) is achieved by colloid-templated consecutive adsorption of polyanions and polycations followed by decomposition of the templating core. Possible areas of application for these shells range from the pharmaceutical, food, cosmetic, and paint industries to catalysis and microcrystallization.
TL;DR: A detailed study of the role that solution pH plays in the layer-by-layer processing of the weak polyelectrolytes poly(acrylic acid) and poly(allylamine hydrochoride) was carried out as discussed by the authors.
Abstract: A detailed study of the role that solution pH plays in the layer-by-layer processing of the weak polyelectrolytes poly(acrylic acid) and poly(allylamine hydrochoride) was carried out. It was found that dramatically different polymer adsorption behavior is observed as one systematically increases (or decreases) the charge density of a weak polyelectrolyte including transitions from very thick adsorbed layers (ca. 80 A) to very thin adsorbed layers (ca. 4 A) over a very narrow pH range. By controlling pH, it is possible to vary the thickness of an adsorbed polycation or polyanion layer from 5 to 80 A. In addition, control over the bulk and surface composition of the resultant multilayer thin films is readily achieved via simple pH adjustments. These studies have provided new insights into the polyelectrolyte sequential adsorption process and have already opened up some interesting technological applications.
TL;DR: In this article, the authors summarize the current development of theoretical models describing properties of polyelectrolyte solutions and adsorption of charged polymers at surfaces and interfaces, and discuss conformational properties and the phenomenon of counterion condensation.
TL;DR: A polymer is described that undergoes marked solubility changes in water in response to temperature and/or pH changes and it is found that block copolymers, in which the temperature- and pH-sensitive units alternate along the chain, show similar behaviour.
Abstract: There are many potential applications of 'intelligent' aqueous polymer systems in medicine, biotechnology, industry and in environmental problems. Many of these polymer systems undergo reversible phase transitions--for example, abrupt changes in volume--in response to external stimuli such as temperature, pH or the nature of the solvent. Most of the polymers studied previously are responsive to only one kind of stimulus. But for some applications, independent responsiveness to several factors, such as temperature and pH, may be required. Here we describe a polymer that undergoes marked solubility changes in water in response to temperature and/or pH changes. The polymer is prepared by grafting temperature-sensitive side chains onto a pH-sensitive backbone. We also find that block copolymers, in which the temperature- and pH-sensitive units alternate along the chain, show similar behaviour.