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Gel phases

For structures with a high curvature (e.g., small micelles) or situations where orientational interactions become important (e.g., the gel phase of a membrane) lattice-based models might be inappropriate. Off-lattice models for amphiphiles, which are quite similar to their counterparts in polymeric systems, have been used to study the self-assembly into micelles [ ], or to explore the phase behaviour of Langmuir monolayers [ ] and bilayers. In those systems, various phases with a nematic ordering of the hydrophobic tails occur. [Pg.2377]

The primary site of action is postulated to be the Hpid matrix of cell membranes. The Hpid properties which are said to be altered vary from theory to theory and include enhancing membrane fluidity volume expansion melting of gel phases increasing membrane thickness, surface tension, and lateral surface pressure and encouraging the formation of polar dislocations (10,11). Most theories postulate that changes in the Hpids influence the activities of cmcial membrane proteins such as ion channels. The Hpid theories suffer from an important drawback at clinically used concentrations, the effects of inhalational anesthetics on Hpid bilayers are very small and essentially undetectable (6,12,13). [Pg.407]

Polymerization in two phases, the Hquid monomer phase and the swollen polymer gel phase, forms the basis for kinetic descriptions of PVC polymerization (79—81). The polymerization rate is slower in the Hquid monomer phase than in the swoUen polymer gel phase on account of the greater mobiHty in Hquid monomer, which allows for greater termination efficiency. The lack of mobiHty in the polymer gel phase reduces termination and creates a higher concentration of radicals, thus creating a higher polymerization rate. Thus the polymerization rate increases with conversion to polymer. [Pg.501]

Quantity Gel phase (19°C, 12 water molecules/lipid) Liquid crystal phase (50°C, 28 water molecules/lipid) ... [Pg.471]

Other possibilities are the reduction of nitro groups by applying the sample solutions to adsorbent layers containing zinc dust and then exposing to hydrochloric acid vapors [110] 3,5-Dinitrobenzoates and 2,4-dinitrophenylhydrazones can also be reduced in the same way on tin-containing silica gel phases [111] Cellulose layers are also suitable for such reactions [112] Seiler and Rothweiler have described a method of trans-salting the alkali metal sulfates to alkali metal acetates [113]... [Pg.77]

An inorganic membrane can be prepared by various methods such as sol-gel, phase separation and leaching.2,3 The sol-gel process is considered the most practical method among those used to prepare inorganic membrane. Sol-gel processing is a simple technology in principle but requires considerable effort to become of practical use. The advantage of this... [Pg.379]

The sol-gel transition has been determined visually, with calcium and copper, for different pectins under different external conditions. As shown in Figure 5 for sample C44 the homogeneous gel phase is situated between the two transition lines. The extension of this phase was found to depend mainly on the DE, temperature and nature of the cation. With calcium the amount of cation required to get a gel increased with the degree of esterification and above 50% it became impossible to get a gel [8]. [Pg.41]

On the opposite, with copper, gels were obtained more easily for high methoxyl pectins. In general the extension of the gel phase was larger with calcium than with copper. [Pg.41]

Contrary to the phase separation curve, the sol/gel transition is very sensitive to the temperature more cations are required to get a gel phase when the temperature increases and thus the extension of the gel phase decreases [8]. The sol/gel transition as determined above is well reproducible but overestimates the real amount of cation at the transition. Gelation is a transition from liquid to solid during which the polymeric systems suffers dramatic modifications on their macroscopic viscoelastic behavior. The whole phenomenon can be thus followed by the evolution of the mechanical properties through dynamic experiments. The behaviour of the complex shear modulus G (o)) reflects the distribution of the relaxation time of the growing clusters. At the gel point the broad distribution of... [Pg.41]

The problem of transport of molecules through swollen gels is of general interest. It not only pertains to catalysis, but also to the field of chromatographic separations over polymeric stationary phases, where the partition of a solute between the mobile phase (liquid phase) and a swollen polymeric stationary phase (gel phase) is a process of the utmost importance. As with all the chemical and physicochemical processes, the thermodynamic and the kinetic aspect must be distinguished also in partition between phases. [Pg.219]

To summarize, there is a sizable and self-consistent body of data indicating that rotational and translational mobility of molecules inside swollen gel-type CFPs are interrelated and controlled mainly by viscosity. Accordingly, T, self-diffusion and diffusion coefficients bear the same information (at least for comparative purposes) concerning diffusion rates within swollen gel phases. However, the measurement of r is by far the most simple (it requires only the collection of a single spectrum). For this reason, only r values have been used so far in the interpretation of diffusion phenomena in swollen heterogeneous metal catalysts supported on CFPs [81,82]. [Pg.222]

Verdugo, P. Polymer Gel Phase Transition in Condensation-Decondensation of Secretory Products, VoL 110, pp. 145-156,... [Pg.216]

Hirst, A.R., Escuder, B. and Miravet, J.F. and Smith, D.K. (2008) High-tech applications of self-assembling supramolecular nanostructured gel-phase materials from regenerative medicine to electronic devices. Angewandte Chemie International Edition, 47 (42), 8002-8018. [Pg.280]

Dicker F.L., Hayden O., Bioimprinting of polymers and sol-gel phases. Selective detection of yeast with imprinted polymers. Anal. Chem. 2002 74 1302-1306. [Pg.385]


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A-gel phase

Amphiphilic Gels for Solid Phase Synthesis

Bonded Phase Silica Gels

Cholesteric gels liquid crystal phase

Fluorous reverse phase silica gel

Fluorous reversed-phase silica gel

Gel Emulsions - Relationship between Phase Behaviour and Formation

Gel Phases (L)

Gel mobile phase

Gel phase diagram

Gel phase diffusion

Gel phase immiscibility

Gel phase properties

Gel phase transition

Gel phases ceramics

Gel phases domain morphology

Gel phases drug delivery

Gel phases foam stabilization

Gel phases rheology

Gel phases structure

Gel phases surfactant-polymer systems

Gel phases vesicle bilayers

Gel-like phase

Gel-liquid crystal phase transition

Gel-liquid crystalline phase transition

Gel-phase 13C NMR spectroscopy

Gel-phase NMR

Gel-phase NMR spectroscopy

Gel-solution phase transition

Gel-state phase

Gel-to-liquid crystalline phase transition

Gels multiple phases

Gibbs phase rule, gels

In gel phase

Interdigitated gel phases

Lipid, gel phase

Liquid-Phase Synthesis Method (Sol-Gel Technique)

Multi-phase gels

Phase diagrams of thermoreversible gels

Phase separation in gels

Phase sol-gel

Phase transition temperatures gels, counterions

Phase transitions in polyelectrolyte gels

Relationship between Phase Behaviour and Spontaneous Gel Emulsion Formation

Response of Gel-Phase Membranes

Reverse phase silica gel

Reversed Phase Bonded Silica Gels

Reversed phase chemically bonded silica gel

Reversed-phased silica gel column chromatography cleanup

Silica Gel-based Stationary Phase Materials

Silica gel stationary phases

Silica gels adsorbant, solid phase extraction

Silica gels mobile phases

Silica gels phase complex

Single-phase gels

Single-phase gels mechanical properties

Sol-Gel Stationary Phases

Sol-gel phase transformation

Sol-gel phase transition

Sol-to-gel phase diagram

Solid-phase extractions with fluorous silica gel

Volume phase transition isotropic gels

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