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Diffusion inner

Poly(N-(p-cyanobenzylidene)-p-aminostyrene), (PCBAS). Polymerization of the monomer from the nematic and isotropic states proceeds over a few hour period (10). Samples polymerized at 127 C for 24 hours show a very weak diffuse inner ring at 29 4.2 degrees. This is much less intense than expected from comparisons with low molecular weight nematics. Within the outer halo there is a sharp line corresponding to 4.43. Films of the polymer are transparent, but are weakly birefringent. Light of low intensity is transmitted between crossed polarizers in the optical microscope. [Pg.7]

Weak diffuse inner ring. Strong diffuse outer ring. [Pg.81]

At first we tried to explain the phenomenon on the base of the existence of the difference between the saturated vapor pressures above two menisci in dead-end capillary [12]. It results in the evaporation of a liquid from the meniscus of smaller curvature ( classical capillary imbibition) and the condensation of its vapor upon the meniscus of larger curvature originally existed due to capillary condensation. We worked out the mathematical description of both gas-vapor diffusion and evaporation-condensation processes in cone s channel. Solving the system of differential equations for evaporation-condensation processes, we ve derived the formula for the dependence of top s (or inner) liquid column growth on time. But the calculated curves for the kinetics of inner column s length are 1-2 orders of magnitude smaller than the experimental ones [12]. [Pg.616]

If a fluid is placed between two concentric cylinders, and the inner cylinder rotated, a complex fluid dynamical motion known as Taylor-Couette flow is established. Mass transport is then by exchange between eddy vortices which can, under some conditions, be imagmed as a substantially enlranced diflfiisivity (typically with effective diflfiision coefficients several orders of magnitude above molecular difhision coefficients) that can be altered by varying the rotation rate, and with all species having the same diffusivity. Studies of the BZ and CIMA/CDIMA systems in such a Couette reactor [45] have revealed bifiircation tlirough a complex sequence of front patterns, see figure A3.14.16. [Pg.1112]

Potentiometric electrodes also can be designed to respond to molecules by incorporating a reaction producing an ion whose concentration can be determined using a traditional ion-selective electrode. Gas-sensing electrodes, for example, include a gas-permeable membrane that isolates the ion-selective electrode from the solution containing the analyte. Diffusion of a dissolved gas across the membrane alters the composition of the inner solution in a manner that can be followed with an ion-selective electrode. Enzyme electrodes operate in the same way. [Pg.532]

McKillop and associates have examined the electrophoretic separation of alkylpyridines by CZE. Separations were carried out using either 50-pm or 75-pm inner diameter capillaries, with a total length of 57 cm and a length of 50 cm from the point of injection to the detector. The run buffer was a pH 2.5 lithium phosphate buffer. Separations were achieved using an applied voltage of 15 kV. The electroosmotic flow velocity, as measured using a neutral marker, was found to be 6.398 X 10 cm s k The diffusion coefficient,... [Pg.619]

A number of chemiluminescent reactions have been studied by producing key reactants through pulsed electric discharge, by microwave dissociation, or by observing the reactions of atoms and free radicals produced in the inner cone of a laminar flame as they diffuse into the flame s cool outer cone (182,183). These are either combination reactions or atom-transfer reactions involving transfer of chlorine (184) or oxygen atoms (181,185—187), the latter giving excited oxides. [Pg.270]

Fig. 1. Schematic representation of the electrochemical or diffuse double layer showing the inner (IHP) and outer (OHP) Helmholtz planes and the... Fig. 1. Schematic representation of the electrochemical or diffuse double layer showing the inner (IHP) and outer (OHP) Helmholtz planes and the...
Either the and the two e s diffuse outward through the film to meet the 0 at the outer surface, or the oxygen diffuses inwards (with two electron holes) to meet the at the inner surface. The concentration gradient of oxygen is simply the concentration in the gas, c, divided by the film thickness, x and the rate of growth of the film dx/dt is obviously proportional to the flux of atoms diffusing through the film. So, from Pick s Law (eqn. (18.1)) ... [Pg.216]

Fig. 8. Diffraction space according to the "disordered stacking model" (a) achiral (zigzag) tube (b) chiral tube. The parallel circles represent the inner rims of diffuse coronae, generated by streaked reflexions. The oo.l nodes generate sharp circles. In (a) two symmetry related 10.0 type nodes generate one circle. In the chiral case (b) each node generates a separate corona [9]. Fig. 8. Diffraction space according to the "disordered stacking model" (a) achiral (zigzag) tube (b) chiral tube. The parallel circles represent the inner rims of diffuse coronae, generated by streaked reflexions. The oo.l nodes generate sharp circles. In (a) two symmetry related 10.0 type nodes generate one circle. In the chiral case (b) each node generates a separate corona [9].
The main predictions of the scaling theory [40], concerning the dynamics behavior of polymer chains in tubes, deal with a number of characteristic times the smallest time rtube measures the interval of essentially Rouse relaxation before the monomers feel the tube constraints significantly, 1 < Wt < Wrtube = and diffusion of an inner monomer is... [Pg.584]

The model just presented describes what electrochemists call the diffuse part of the double layer and no account is made of the inner layer effects such as the plane of the closest approach. To have an idea what the impact of the effects predicted by this model on the measured capacitance could be, we assume the traditional inner and diffuse layer separation. However, we... [Pg.830]

Mitochondria are surrounded by a simple outer membrane and a more complex inner membrane (Figure 21.1). The space between the inner and outer membranes is referred to as the intermembrane space. Several enzymes that utilize ATP (such as creatine kinase and adenylate kinase) are found in the intermembrane space. The smooth outer membrane is about 30 to 40% lipid and 60 to 70% protein, and has a relatively high concentration of phos-phatidylinositol. The outer membrane contains significant amounts of porin —a transmembrane protein, rich in /3-sheets, that forms large channels across the membrane, permitting free diffusion of molecules with molecular weights of about 10,000 or less. Apparently, the outer membrane functions mainly to... [Pg.674]

The final step of the reaction involves the transfer of two electrons from iron-sulfur clusters to coenzyme Q. Coenzyme Q is a mobile electron carrier. Its isoprenoid tail makes it highly hydrophobic, and it diffuses freely in the hydrophobic core of the inner mitochondrial membrane. As a result, it shuttles electrons from Complexes I and II to Complex III. The redox cycle of UQ is shown in Figure 21.5, and the overall scheme is shown schematically in Figure 21.6. [Pg.682]

As with Complex 1, passage of electrons through the Q cycle of Complex 111 is accompanied by proton transport across the inner mitochondrial membrane. The postulated pathway for electrons in this system is shown in Figure 21.12. A large pool of UQ and UQHg exists in the inner mitochondrial membrane. The Q cycle is initiated when a molecule of UQHg from this pool diffuses to a site (called Q, ) on Complex 111 near the cytosolic face of the membrane. [Pg.687]

It should be emphasized here that the four major complexes of the electron transport chain operate quite independently in the inner mitochondrial membrane. Each is a multiprotein aggregate maintained by numerous strong associations between peptides of the complex, but there is no evidence that the complexes associate with one another in the membrane. Measurements of the lateral diffusion rates of the four complexes, of coenzyme Q, and of cytochrome c in the inner mitochondrial membrane show that the rates differ considerably, indicating that these complexes do not move together in the membrane. Kinetic studies with reconstituted systems show that electron transport does not operate by means of connected sets of the four complexes. [Pg.691]


See other pages where Diffusion inner is mentioned: [Pg.1537]    [Pg.233]    [Pg.234]    [Pg.1323]    [Pg.10]    [Pg.146]    [Pg.2002]    [Pg.1537]    [Pg.233]    [Pg.234]    [Pg.1323]    [Pg.10]    [Pg.146]    [Pg.2002]    [Pg.178]    [Pg.2723]    [Pg.90]    [Pg.91]    [Pg.233]    [Pg.252]    [Pg.338]    [Pg.49]    [Pg.289]    [Pg.488]    [Pg.49]    [Pg.63]    [Pg.31]    [Pg.221]    [Pg.124]    [Pg.193]    [Pg.326]    [Pg.100]    [Pg.470]    [Pg.131]    [Pg.576]    [Pg.831]    [Pg.831]    [Pg.857]    [Pg.315]    [Pg.691]    [Pg.171]    [Pg.156]   
See also in sourсe #XX -- [ Pg.239 ]

See also in sourсe #XX -- [ Pg.239 ]

See also in sourсe #XX -- [ Pg.239 ]




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Inner diffusion boundary layer

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