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Polyelectrolyte layers

Electrophoresis measurements provide a qualitative indication of the assembly of polymer multilayers on colloids [49,50], The -potential as a function of polyelectrolyte layer number for negatively charged polystyrene (PS) particles coated with poly(diallyldimethylam-monium chloride) (PDADMAC) and poly(styrenesulfonate) (PSS) are displayed in Figure... [Pg.510]

FIG. 9 Confocal laser scanning micrograph of a hollow polymer capsule. The polymer capsule was obtained from polymer multilayer-templated FDA microcrystals after removal of the colloidal core. The FDA microcrystals were coated with SDS and 11 polyelectrolyte layers [(PAH/PSS)3/PAH/ (PSS/PAH-FITC)2]. (PAH-FITC = PAH labeled with fluorescein isothiocyanate.) The microcrystal core was removed by exposure of the coated microcrystals to ethanol, causing solubilization of FDA. [Pg.518]

Measurement results utilizing polyelectrolyte layers and synthetic DNA... [Pg.210]

MEASUREMENT RESULTS UTILIZING POLYELECTROLYTE LAYERS AND SYNTHETIC DNA... [Pg.228]

Since the components in the adsorbed polyelectrolyte layer are considered to be the same as the bulk phase with a three component system which consists of polyelectrolyte, simple salt, and water, we calculate the adsorbances of polyelectrolyte and salt by assuming the Donnan equilibrium between the bulk phase and the adsorbed polyelectrolyte layer, as described previously (5). [Pg.41]

The developed sensor was used for ultrathin-film measurement. The reflection spectrum was shifted during the deposition of thin films (e.g., self-assembly of polyelectrolyte layers) onto the sensor end. The reflection between the thin film and the fiber endface was neglected because of their similar refractive indices. As the film increased its thickness, the length of the fiber cavity changed. The amount of change was estimated by the phase shift of the interferogram. The device could also be used as an immunosensor in which the optical thickness changes were used to... [Pg.151]

In many biological systems the biological membrane is a type of surface on which hydrophilic molecules can be attached. Then a microenvironment is created in which the ionic composition can be tuned in a controlled way. Such a fluffy polymer layer is sometimes called a slimy layer. Here we report on the first attempt to generate a realistic slimy layer around the bilayer. This is done by grafting a polyelectrolyte chain on the end of a PC lipid molecule. When doing so, it was found that the density in which one can pack such a polyelectrolyte layer depends on the size of the hydrophobic anchor. For this reason, we used stearoyl Ci8 tails. The results of such a calculation are given in Figure 26. [Pg.84]

Emerging new technologies such as spray deposition of alternate polyelectrolyte layers in LbL multilayers will reduce the deposition time to 1 s per layer, which will open up possibilities of real applications in electrochemical science and technology. [Pg.107]

Kawaguchi et al.125) prepared an ionene-oxyethylene-ionene (IEI) triblock copolymer with the molecular weight 72 X 103 and measured its surface tension in aqueous KBr. They also determined by ellipsometry the adsorbance and the thickness of the adsorbed polyelectrolyte layer at the air-KBr solution interface as a function of the KBr concentration. The data obtained indicate that this copolymer is surface-active and that the effect of added KBr on the surface tension is stronger than in the case of polyoxyethylene (POE). [Pg.60]

Because the Donnan exclusion effect is much stronger for multivalent ions than for univalent ions, the polyelectrolyte layer rejects multivalent ions but allows the univalent ions to pass relatively unhindered. [Pg.417]

Hard-sphere or cylinder models (Avena et al., 1999 Benedetti et al., 1996 Carballeira et al., 1999 De Wit et al., 1993), permeable Donnan gel phases (Ephraim et al., 1986 Marinsky and Ephraim, 1986), and branched (Klein Wolterink et al., 1999) or linear (Gosh and Schnitzer, 1980) polyelectrolyte models were proposed for NOM. Here the various models must be differentiated in detail—that is, impermeable hard spheres, semipermeable spherical colloids (Marinsky and Ephraim, 1986 Kinniburgh et al., 1996), or fully permeable electrolytes. The latest new model applied to NOM (Duval et al., 2005) incorporates an electrokinetic component that allows a soft particle to include a hard (impermeable) core and a permeable diffuse polyelectrolyte layer. This model is the most appropriate for humic substances. [Pg.507]

Radtchenko IL, Sukhorukov GB, Leporatti S, Khomutov GB, Donath E, Mohwald H. Assembly of alternated multivalent ion/polyelectrolyte layers on colloidal particles. Stability of the multilayers and encapsulation of macromolecules into polyelectrolyte capsules. Journal of Colloid Interface Science 2000, 230, 272-280. [Pg.315]

Mesoporous silica containers can be used as inhibitor hosts with controlled release properties triggered at the beginning of the corrosion process in response to local pH changes. For instance, mesoporous silica nanoparticles covered with polyelectrolyte layers can be loaded with an inhibitor (2-(benzothiazol-2-ylsulfanyl)-succinic acid) prior to introduction into a hybrid zirconia-silica sol-gel film. This hierarchical design avoids spontaneous release of the inhibitor by the formation of a polyelectrolyte shell over the container s outermost surface. [Pg.642]

To make the containers sensitive to IR laser light, preformed silver nanoparticles were directly incorporated into the polyelectrolyte shell. For this purpose, AgNPs were added into solutions of polyelectrolytes for LbL deposition and hence fixed between the polyelectrolyte layers. The AFM images of the resultant nanocontainer-impregnated him showed a uniform distribution of the containers over the coating, with the concentration of the silica containers equalling 107 containers per meter squared. [Pg.650]

Abstract Polyelectrolyte block copolymers form micelles and vesicles in aqueous solutions. Micelle formation and micellar structure depends on various parameters like block lengths, salt concentration, pH, and solvent quality. The synthesis and properties of more complicated block and micellar architectures such as triblock- and graft copolymers, Janus micelles, and core-shell cylinder brushes are reviewed as well. Investigations reveal details of the interactions of polyelectrolyte layers and electro-steric stabilization forces. [Pg.173]

In dilute aqueous solutions, polyelectrolyte block copolymers self-assemble into micelles consisting of a hydrophobic core and a polyelectrolyte shell. The study of their structural properties is expected to provide a basic understanding of the properties of dense polyelectrolyte layers, electro-steric stabilization mechanisms, and actuator functions based on variations in the electrostatic interactions. [Pg.175]


See other pages where Polyelectrolyte layers is mentioned: [Pg.10]    [Pg.11]    [Pg.13]    [Pg.145]    [Pg.228]    [Pg.510]    [Pg.511]    [Pg.517]    [Pg.517]    [Pg.151]    [Pg.217]    [Pg.429]    [Pg.229]    [Pg.230]    [Pg.263]    [Pg.115]    [Pg.84]    [Pg.80]    [Pg.24]    [Pg.59]    [Pg.66]    [Pg.67]    [Pg.193]    [Pg.177]    [Pg.185]    [Pg.341]    [Pg.180]    [Pg.215]    [Pg.416]    [Pg.265]    [Pg.648]    [Pg.131]    [Pg.164]   
See also in sourсe #XX -- [ Pg.131 ]




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