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In-gel

A diffusion mechanism is also used in dialysis as a means of separating colloids from crystalloids. The rate of diffusion of molecules in gels is practically the same as in water, indicating the continuous nature of the aqueous phase. The diffusion of gases into a stream of vapour is of considerable importance in diffusion pumps. [Pg.137]

Sephadex A trade name for an insoluble hydrophilic substance prepared by cross-linking dextran, and used in gel filtration. It can also be linked to acidic or basic groups for ion exchange or to alkanes for the chromatography of lipophilic compounds. [Pg.356]

Salt Effects. The definition of a capacity factor k in hydrophobic interaction chromatography is analogous to the distribution coefficient, in gel permeation chromatography ... [Pg.56]

Konjac flour, derived from the konjac plant tuber, has a long history of use in the Ear East, but is a newcomer to the United States. It reacts with many starches to enhance the viscosity of both, and is used in gels that are stable in boiling water. [Pg.119]

The weatherabihty and hydrolytic stabiUty of unsaturated polyesters based on neopentyl glycol have made it a popular intermediate for use in formulations exposed to severe conditions, eg, in gel coats for cultured marble and marine appHcations (see Coatings, marine) (13). [Pg.372]

In gel-forming processes, the reactive aluminosibcate gel is first formed into a pellet which reacts with sodium aluminate solution and caustic solution. The 2eobte crysta11i2es in situ within an essentiaby self-bonded pellet, or as a component in an unconverted amorphous matrix. [Pg.453]

Polymer-based, synthetic ion-exchangers known as resins are available commercially in gel type or truly porous forms. Gel-type resins are not porous in the usual sense of the word, since their structure depends upon swelhng in the solvent in which they are immersed. Removal of the solvent usually results in a collapse of the three-dimensional structure, and no significant surface area or pore diameter can be defined by the ordinaiy techniques available for truly porous materials. In their swollen state, gel-type resins approximate a true molecular-scale solution. Thus, we can identify an internal porosity p only in terms of the equilibrium uptake of water or other liquid. When crosslinked polymers are used as the support matrix, the internal porosity so defined varies in inverse proportion to the degree of crosslinkiug, with swelhng and therefore porosity typically being more... [Pg.1500]

The commercial polymers are of comparatively low molecular weight (M = 25 000-60 000) and whilst being essentially linear may contain a few branches or cross-links arising out of thermal oxidation. Exposure to ultraviolet light causes a rapid increase in gel content, whilst heating in an oven at 125°C causes gelation only after an induction period of about 1000 hours. Eor outdoor applications it is necessary to incorporate carbon black. The polymers, however, exhibit very good hydrolytic stability. [Pg.587]

Where a flexible resin is required adipic and, rarely, sebacic acids are used. Whereas the phthalic acids give a rigid link these materials give highly flexible linkages and hence flexibility in the cured resin. Flexible resins are of value in gel coats. [Pg.699]

A novel cross-linked polystyrene-divinylbenzene copolymer has been produced from suspension polymerization with toluene as a diluent, having an average particle size of 2 to 50 /rm, with an exclusive molecular weight for the polystyrene standard from about 500 to 20,000 in gel-permeation chromatography. A process for preparing the PS-DVB copolymer by suspension polymerization in the presence of at least one free-radical polymerization initiator, such as 2,2 -azo-bis (2,4-dimethylvaleronitrile) with a half-life of about 2 to 60 min at 70°C, has been disclosed (78). [Pg.22]

The packing material for liquid chromatography is produced from styrene and divinylbenzene dissolved in 50 to 300% by weight of organic solvent to both monomers. The constitution of divinylbenzene in the monomer mixture is not less than 60% by weight. In gel-permeation chromatography, the exclusive molecular weight is not less than 1 X 10 in terms of standard polystyrene (79). [Pg.22]

Macroporous polyvinyl alcohol particles with a molecular weight cutoff of ca. 8 X 10 in gel-permeation chromatography have been prepared. The particles are produced by first dispersing an aqueous solution of polyvinyl alcohol in an organic solvent to make spheres of polyvinyl alcohol solution. Holding the dispersion in such a state that a gel will then form spontaneously will cause the gel to react with glutaraldehyde in the presence of an acidic catalyst (85). [Pg.23]

Classical gel electrophoresis has been used extensively for protein and nucleic acid purification and characterization [9, 10], but has not been used routinely for small molecule separations, other than for polypeptides. A comparison between TLC and electrophoresis reveals that while detection is usually accomplished off-line in both electrophoretic and TLC methods, the analyte remains localized in the TLC bed and the mobile phase is immediately removed subsequent to chromatographic development. In contrast, in gel electrophoresis, the gel matrix serves primarily as an anti-... [Pg.289]

A series of polyamine disulphides (polyaniline disulphide, polyamine disulphide, and polyparaphenylenedi-amine disulphide) represent effective thermostabilizers of cured polyethylene, and provide a decrease in gel fraction 2.5-3 times as large as that in case of inhibited thermal destruction. Stabilizers of normal polyethylene (Neozone D , Santonox R ) are inefficient as stabilizers of cured polyethylene, these substances decompose and even initiate thermal destruction of cured polyethylene. [Pg.90]

Polyamine disulphides are effective thermostabilizers of cured polyethylene up to 400°C. In presence of polyamine disulphides a decrease in gel fraction is one half as large as that of nonstabilized cured polyethylene over the temperature range from 350-380°C [46]. [Pg.90]

A drop in gel fraction of nonstabilized cured polyethylene amounts to 50% after 25-h exposure, 75% after 50 hours and after a 75-h exposure the complete fall is observed. At the same time, a decrease in gel fraction in presence of polyaniline disulphide is observed only after a 50-h exposure and comes to only 2%, whereas... [Pg.90]

Wang et al.2 and Najafpour et al.3A worked with immobilised microbial cells of Nitrobacer agilis, Saccharomyces cerevisiae and Pseudomonas aeruginosa in gel beads, respectively. They found separately that the cells retained more than 90% of their activity after immobilisation by using specific oxygen uptake rate (SOUR) [mg 02g 1 (dry biomass) h 11 as the biomass activity indicator. Such differences in immobilised biomass and activity between free and immobilised biomass activities depend strongly on the particular characteristics of the microbial systems and their interaction with the support matrix. [Pg.200]


See other pages where In-gel is mentioned: [Pg.89]    [Pg.51]    [Pg.228]    [Pg.353]    [Pg.69]    [Pg.359]    [Pg.296]    [Pg.298]    [Pg.300]    [Pg.453]    [Pg.253]    [Pg.307]    [Pg.163]    [Pg.251]    [Pg.488]    [Pg.296]    [Pg.2061]    [Pg.9]    [Pg.22]    [Pg.219]    [Pg.234]    [Pg.90]    [Pg.90]    [Pg.90]    [Pg.90]    [Pg.91]    [Pg.91]    [Pg.224]    [Pg.451]    [Pg.515]    [Pg.6]    [Pg.188]    [Pg.1029]    [Pg.392]   
See also in sourсe #XX -- [ Pg.546 , Pg.548 ]

See also in sourсe #XX -- [ Pg.534 , Pg.537 ]




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A Robust Approach to Inorganic Aerogels The Use of Epoxides in Sol-Gel Synthesis

AGM and gel technology in vehicles

Antibody-antigen interactions in gels

Antigen-Antibody Reactions in Gels

Application of alkoxides in sol-gel processes

Autoradiography of Radioactive Labeled Compounds in Gels

Biomolecules, interactions and stability in sol-gel matrices

Carbon Gels in Catalysis

Cation effects, in silica gel formation

Concentration effects, in silica gel formation

Cracks in gels

Cross-linking in gels

Crystal growth in gels

Crystallization in Sol-Gel-Derived Films Raman Spectra

Crystals, growth of, in silica gel

Detecting Glycoproteins in Gels

Differential in-gel electrophoresis

Diffusion coefficient in gels

Diffusion in biological gels

Diffusivity in biological gels

Donnan-Type Equilibria in Polyelectrolyte Gels

Effective Diffusivities in Biological Gels

Electrochemical Measurement of Solute in Gels

Electrodes in a Plane with Fix-Ended Gel

Electrodes in a Plane with Free-Ended Gel

Electrophoretic mobility in gels

Electrophoretic separation in agar gel

Encapsulation in Sol-Gel Matrices

Entrapment in Gel Matrixes

Experimentally Observed Gel Points in Polyfunctional Condensations

Fluorescence of Polymers in Gel State

Fractionation of Polyacrylamide by Gel Permeation Chromatography in Water

Gel Electrophoresis in Analyzing Dendritic Polymers and Related Materials

Gel Electrophoresis in CE

Gel aging, in zeolite crystallization

Gel electrophoresis in the presence of SDS

Gel polymer electrolytes in lithium ion batteries

Gels Cross-Linked in Solution

Gels in Good Solvents

Glycoproteins in gels

Growth in Gels

Hybridization in gel

Hydrophobicity of sugars as evidenced by their affinity for polystyrene gel in aqueous media

Immunochemical reactions in agar gel

In gel chromatography

In gel permeation chromatography

In gel phase

In sol-gel methods

In-Situ Studies on Sol-Gel Systems

In-gel digestion

In-gel digests

In-gel fluorescence

In-gel trypsin digestion

In-gel tryptic digestion

In-vivo gel formation

Interactions and stability of biomolecules in sol-gel

Intermittent Crosslinked Gels in a Film Product

Isoelectric focusing in polyacrylamide gel

Light scattering in gels

Mechanism in the formation of polysaccharide gels

Molecular Diffusion in Biological Solutions and Gels

NMR Relaxivity Properties Applications of Sol-Gel Procedures in MRI Contrast Agents

NMR in gels and porous media

Particle Size of Ag NPs in Sol-Gel Films from Optical Absorption Spectra

Pattern Formation in Variety of Gels

Pb in Sol-Gel Prepared Ceramics

Phase separation in gels

Phase transitions in polyelectrolyte gels

Plant and animal whole cells, in sol-gel matrices

Platinized silica gel, in preparation

Platinized silica gel, in preparation of HBr

Porosity and dynamics of proteins in sol-gel

Preparative electrophoresis in polyacrylamide gel

Probes in gels and biological systems

Progress in sol-gel process

Quantum Dots in Sol-Gel Films for NLO Effects

Relevant Examples in the Field of Sol-Gel Materials

Removing Gels Produced in Polymerization

Resolution power and calibration in gel chromatography

Results from Concentrated Electrolyte Additions and 1 Phenol in Agarose Gels

Results from Dilute Electrolyte Additions and pH Changes in Agarose Gels

Role of Biopolymers in Sol-Gel Processing

SEI formation in solid polymer and gel electrolytes

Scandium triflate silica gel, in lactonization

Self-assembly of ionic surfactants in oppositely charged polyelectrolyte gels

Silica gel in alkali metal hydroxides

Silica gel in thin-layer chromatography

Silica gel platinized, use in preparation

Silica gel, use in separation

Silver Staining of Proteins in Gels

Small Gels in an LLDPE Film Product

Sol-Gel Transition in Semidilute Conditions

Solutes in gels

Solvent water, in gels

Solvents in gels

Strain-induced alignment in a gel

Studies in solutions and gels

Supramolecular Gels in Aqueous and Polar Organic Media

TRICINE-SDS-Polyacrylamide Gel Electrophoresis for Proteins and Oligopeptides in the Range of 1000-50 000 Daltons

The Electrical Contacting of Enzymes in Mediator-functionalized Sol-gel Matrices

Theory of Deformation and Flow in Gels

Variation in gel composition

Water in gel

Whole-cell encapsulation in sol-gels and their applications

Whole-cell encapsulation, in sol-gels

Whole-cell encapsulation, in sol-gels plant and animal cells

Zone Electrophoresis in Starch Gels and

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