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Relative mobility

The use of standards with samples makes zone electrophoresis particulady usehil as an analytical tool. However, when samples caimot be analyzed on the same gel, differences in the experimental conditions from experiment to experiment make direct comparison more difficult. To make comparisons from experiment to experiment, a relative mobility, is often measured by measuring the distance a component travels down the gel compared to some reference or standard component. [Pg.180]

The polysulphides used are relatively mobile liquids with viscosities of about 10 poise and are thus useful as reactive diluents. They may be employed in any ratio with epoxide and produets will range from soft rubbers, where only polysulphides are employed, to hard resins using only epoxide. [Pg.769]

Where is the ratio of the irradiated to unirradiated elastic modulus. The dislocation pinning contribution to the modulus change is due to relatively mobile small defects and is thermally annealable at 2000°C. Figure 13 shows the irradiation-induced elastic modulus changes for GraphNOL N3M. The low dose change due to dislocation piiming (dashed line) saturates at a dose <1 dpa. [Pg.467]

Most organic reactions are done in solution, and it is therefore important to recognize some of the ways in which solvent can affect the course and rates of reactions. Some of the more common solvents can be roughly classified as in Table 4.10 on the basis of their structure and dielectric constant. There are important differences between protic solvents—solvents fliat contain relatively mobile protons such as those bonded to oxygen, nitrogen, or sulfur—and aprotic solvents, in which all hydrogens are bound to carbon. Similarly, polar solvents, those fliat have high dielectric constants, have effects on reaction rates that are different from those of nonpolar solvent media. [Pg.237]

Fig. 22. Nomialized pull-off energy measured for polyethylene-polyethylene contact measured using the SFA. (a) P versus rate of crack propagation for PE-PE contact. Change in the rate of separation does not seem to affect the measured pull-off force, (b) Normalized pull-off energy, Pn as a function of contact time for PE-PE contact. At shorter contact times, P does not significantly depend on contact time. However, as the surfaces remain in contact for long times, the pull-off energy increases with time. In seinicrystalline PE, the crystalline domains act as physical crosslinks for the relatively mobile amorphous domains. These amorphous domains can interdiffuse across the interface and thereby increase the adhesion of the interface. This time dependence of the adhesion strength is different from viscoelastic behavior in the sense that it is independent of rate of crack propagation. Fig. 22. Nomialized pull-off energy measured for polyethylene-polyethylene contact measured using the SFA. (a) P versus rate of crack propagation for PE-PE contact. Change in the rate of separation does not seem to affect the measured pull-off force, (b) Normalized pull-off energy, Pn as a function of contact time for PE-PE contact. At shorter contact times, P does not significantly depend on contact time. However, as the surfaces remain in contact for long times, the pull-off energy increases with time. In seinicrystalline PE, the crystalline domains act as physical crosslinks for the relatively mobile amorphous domains. These amorphous domains can interdiffuse across the interface and thereby increase the adhesion of the interface. This time dependence of the adhesion strength is different from viscoelastic behavior in the sense that it is independent of rate of crack propagation.
Turning now to the Brownian motion of the ion, we must ask to what extent adjacent solvent molecules will tend to accompany the ion in its random motion, as a result of the mutual attraction. It appears that the strength of this mutual attraction will be similar in the three solvents. But we notice that the size of the solvent molecules that tend to accompany the ion is considerably larger in methanol than in water and will be still larger in ethanol. This fact must be taken into account, if we attempt to predict the relative mobilities of the ion in the three solvents. [Pg.72]

The second way in which an electroactive species such as lithium can be incorporated into the structure of an electrode is by a topotactic insertion reaction. In this case the guest species is relatively mobile and enters the crystal structure of the host phase so that no significant change in the structural configuration of the host lattice occurs. [Pg.365]

Research and development into polymer electrolyte battery systems continues, yet many unsolved and controversial issues, particularly relating to the inadequate understanding and control of ion dissociation and the relative mobilities of the ions, remain. Modem computational resources now allow the structures of complex systems such as polymer electrolytes to be simulated and evaluated. Computer simu-... [Pg.520]

NGc, Nitrosamines, Nitramines, etc. In this technique, microgram quantities of a sample are added to a column packed with an absorbing medium or phase. Over this is maintained a flow of mobile phase (gas or liq). The sample components separate because of their relative mobility in the absorbing phase, and thus leave the column at different times (See Vol 1,... [Pg.300]

Fig. 20. Schematic representation of the solid + solid reaction A + B -> AB in which constituents of the relatively mobile reactant (A) are transported to the outer surfaces of the product phase (AB) and rate is controlled by diffusion of constituents of A and/ or B across the barrier layer AB. Fig. 20. Schematic representation of the solid + solid reaction A + B -> AB in which constituents of the relatively mobile reactant (A) are transported to the outer surfaces of the product phase (AB) and rate is controlled by diffusion of constituents of A and/ or B across the barrier layer AB.
The relative immobility of the chlorodioxins is expected, based on the very low solubility of these compounds in water (0.6 / g/liter). In contrast, the herbicide, 2,4,5-T, is relatively mobile in sandy soils, but movement decreases as soil organic matter increases. What does this information tell us, and how does it compare with other organic compounds A mobility scale has been devised for a large number of pesticides (3). Higher mobility numbers reflect increased compound mobility in soils. The dioxins would be in Class 1—i.e., they are immobile in soils and would compare with several chlorinated hydrocarbon insecticides. [Pg.106]

The effect of precursor-support interactions on the surface composition of supported bimetallic clusters has been studied. In contrast to Pt-Ru bimetallic clusters, silica-supported Ru-Rh and Ru-Ir bimetallic clusters showed no surface enrichment in either metal. Metal particle nucleation in the case of the Pt-Ru bimetallic clusters is suggested to occtir by a mechanism in which the relatively mobile Pt phase is deposited atop a Ru core during reduction. On the other hand, Ru and Rh, which exhibit rather similar precursor support interactions, have similar surface mobilities and do not, therefore, nucleate preferentially in a cherry model configuration. The existence of true bimetallic clusters having mixed metal surface sites is verified using the formation of methane as a catalytic probe. An ensemble requirement of four adjacent Ru surface sites is suggested. [Pg.294]

In a typical study of conductivity. Cook (1982) used a cell consisting of two platinum disc electrodes, 12 mm in diameter and 1-5 mm apart. The setting AB cement was examined in this cell which had been calibrated using a standard solution of0 02 M potassium chloride. Plots were recorded of spedfic conductance against time for each of the setting cements. For zinc polycarboxylate there was found to be a rapid drop in spedfic conductance about 10 minutes after the start of mixing. This behaviour was consistent with the replacement of relatively mobile protons by significantly less mobile zinc ions in the polycarboxylate chain. Con-... [Pg.366]

From a structural point-of-view the bulk metallic state, that is, fee lattice (with varying densities of defects such as twins and stacking faults) is generally established in gold nanoparticles of about 10 nm diameter and upwards. However, such particles still display many unusual physical properties, primarily as the result of their small size. Shrinking the size of gold particles has an important effect it increases both the relative proportion of surface atoms and of atoms of even lower coordination number, such as edge atoms [49] and these atoms in turn are relatively mobile and reactive. [Pg.325]

Improvement of the relative mobility of oil to water by biosurfactants and biopolymers... [Pg.217]

Santschi PH, Li YH, Adler DM, Amdurer M, Bell J, Nyffeler UP (1983) The relative mobility of natural (Th, Pb and Po) and fallout (Pu, Am, Cs) radionuclides in the coastal marine-enviromnent - results from model-ecosystems (MERL) and Narragansett Bay. Geochim Cosmochim Acta 47 201-210... [Pg.604]

There are three main electrophoretic methods of separation (i) zone electrophoresis, where the components are separated on a basis of relative mobilities (ii) isotachophoresis, where the separation is again based on relative mobilities but where the solutes are sandwiched between leading and terminating electrolytes ... [Pg.273]

It is clear from the two spectra that resonances corresponding to inner carbohydrate residues, such as peaks 5, 6, and 13, display a much larger line-width than resonances corresponding to outer residues, such as peaks 2-4. This reflects the relative mobility of such residues, and aids in distinguishing between terminal residues and inner residues of the intact oligosaccharide chains of intact glycoproteins. [Pg.19]

An advantage of NMR spectroscopy is the analysis of protein dynamics. Measurement and analysis of the relaxation parameters R1 R2, and the 15N NOE of 15N-labeled proteins leads to an order parameter (S2) that can describe the relative mobility of the backbone of the protein. Both collagenase-1 and stromelysin-1 have been studied either as inhibited complexes or the free protein [19, 52], Stromleysin-1 was studied with inhibitors binding to prime or nonprime subsites. Presence or absence of inhibitors in the nonprime sites had minor effects on the highly ordered structure of residues in these subsites, which are in contact with the... [Pg.87]

To emphasize the difference between the results in different kinds of rock, it is helpful to consider the relative mobility, Ar, which is the ratio of the measured absolute mobility to the rock permeability. The dimension of relative mobility is reciprocal centipoise, whereas absolute mobility is measured in (md/cp). [Pg.507]

Thus, in the very approximate sense in which "foam" is considered to be a single fluid that saturates the porespace (so that singlephase permeability could be used to characterize the rock), the "effective viscosity" of the foam could be taken to be the reciprocal of the relative mobility. [Pg.507]

These tests show that CC -foam is not equally effective in all porous media, and that the relative reduction of mobility caused by foam is much greater in the higher permeability rock. It seems that in more permeable sections of a heterogeneous rock, C02-foam acts like a more viscous liquid than it does in the less permeable sections. Also, we presume that the reduction of relative mobility is caused by an increased population of lamellae in the porous medium. The exact mechanism of the foam flow cannot be discussed further at this point due to the limitation of the current experimental set-up. Although the quantitative exploration of this effect cannot be considered complete on the basis of these tests alone, they are sufficient to raise two important, practical points. One is the hope that by this mechanism, displacement in heterogeneous rocks can be rendered even more uniform than could be expected by the decrease in mobility ratio alone. The second point is that because the effect is very non-linear, the magnitude of the ratio of relative mobility in different rocks cannot be expected to remain the same at all conditions. Further experiments of this type are therefore especially important in order to define the numerical bounds of the effect. [Pg.510]

Tautomerism, strictly defined, could be used to describe the reversible interconversion of isomers, in all cases and under all conditions. In practice, the term has increasingly been restricted to isomers that are fairly readily interconvertible, and that differ from each other only (a) in electron distribution, and (b) in the position of a relatively mobile atom or group. The mobile atom is, in the great majority of examples, hydrogen, and the phenomenon is then referred to as prototropy. Familiar examples are / -ketoesters, e.g. ethyl 2-ketobutano-ate (ethyl acetoacetate, 23), and aliphatic nitro compounds, e.g. nitro-methane (24) ... [Pg.277]

Fig. 3 SDS-PAGE Photograph Separation (Lane Mr and A) and activity staining (Lane B and C) of the crude filtrate of Funalia trogii. Lane Mr standard molecular weight markers ([3-galactosi-dase, 118.0 kDa bovine serum albumin, 79.0 kDa ovalbumin, 47.0 kDa carbonic anhydrase, 33.0 kDa P-lactoglobulin, 25.0 kDa and lysozyme, 19.5 kDa). Relative mobilities of the standard markers vs. common logarithms of their molecular masses were plotted.With the linear regression output, the molecular masses of the proteins in the crude filtrate were estimated (taken from [18])... Fig. 3 SDS-PAGE Photograph Separation (Lane Mr and A) and activity staining (Lane B and C) of the crude filtrate of Funalia trogii. Lane Mr standard molecular weight markers ([3-galactosi-dase, 118.0 kDa bovine serum albumin, 79.0 kDa ovalbumin, 47.0 kDa carbonic anhydrase, 33.0 kDa P-lactoglobulin, 25.0 kDa and lysozyme, 19.5 kDa). Relative mobilities of the standard markers vs. common logarithms of their molecular masses were plotted.With the linear regression output, the molecular masses of the proteins in the crude filtrate were estimated (taken from [18])...

See other pages where Relative mobility is mentioned: [Pg.181]    [Pg.350]    [Pg.351]    [Pg.74]    [Pg.205]    [Pg.244]    [Pg.500]    [Pg.44]    [Pg.210]    [Pg.645]    [Pg.94]    [Pg.58]    [Pg.258]    [Pg.773]    [Pg.118]    [Pg.470]    [Pg.507]    [Pg.510]    [Pg.516]    [Pg.111]    [Pg.302]    [Pg.40]    [Pg.70]    [Pg.209]   
See also in sourсe #XX -- [ Pg.64 , Pg.240 , Pg.307 , Pg.314 , Pg.341 ]

See also in sourсe #XX -- [ Pg.64 , Pg.240 , Pg.307 , Pg.314 , Pg.341 ]

See also in sourсe #XX -- [ Pg.79 ]

See also in sourсe #XX -- [ Pg.64 , Pg.240 , Pg.307 , Pg.314 , Pg.341 ]

See also in sourсe #XX -- [ Pg.205 , Pg.209 ]




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Mobility reduced/relative

Reciprocal relative mobility

Relative electrophoretic mobility

Relative frontal mobility

Relative hydrogen mobility

Relative mobility, definition

Relative oxygen mobility

Serum proteins relative mobilities

The Relative Mobilities of Serum Protein Fractions

Total relative mobility

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