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Matrix concentration-differences

During ATP synthesis, protons move down these gradients from outside [Hour] into the mitochondrial matrix each proton doing both electrical and osmotic work (due to the concentration difference) so that the Gibbs energy change is... [Pg.148]

Figure 9.8 Simple diagram of mitochondrial H -ion movement and axonal K -ion movement to establish membrane potentials across membranes. Note that H movement from the mitochondrial matrix to the outer surface of the inner membrane requires a specific proton pump that requires energy, which is transferred from electron transfer, whereas the K ion movement occurs via an ion channel with energy provided from the concentration difference of K ions on either side of the membrane (approximately 100-fold). The movement of both the protons and K ions generates a membrane potential. The potential across the membrane of the nerve axon provides the basis for nervous activity (see Chapter 14). Figure 9.8 Simple diagram of mitochondrial H -ion movement and axonal K -ion movement to establish membrane potentials across membranes. Note that H movement from the mitochondrial matrix to the outer surface of the inner membrane requires a specific proton pump that requires energy, which is transferred from electron transfer, whereas the K ion movement occurs via an ion channel with energy provided from the concentration difference of K ions on either side of the membrane (approximately 100-fold). The movement of both the protons and K ions generates a membrane potential. The potential across the membrane of the nerve axon provides the basis for nervous activity (see Chapter 14).
Concentration, Characteristic, or Property Matrix (C) Different characteristics or properties of chemical systems can be predicted using multivariate calibration techniques. Throughout this book, the word concentration is often used as a generic term to represent concentration, characteristic, or property. [Pg.186]

Compound Matrix Concentration LC MS or ELISA GC MS MS % Difference Reference"... [Pg.90]

When a biocatalyst is immobilized on or within a solid matrix, mass transfer effects may exist because the substrate must diffuse from the bulk solution to the immobilized biocatalyst. If the biocatalyst is attached to non-porous supports there are only external mass transfer effects on the catalytically active outer surface in the reaction solution, the supports are surrounded by a stagnant film and substrate and product are transported across this Nemst layer by diffusion. The driving force for this diffusion is the concentration difference between the surface and the bulk concentration of substrate and product. [Pg.422]

Consider a binary system at an elevated temperature composed of A and B atoms containing a distribution of spherical /0-phase particles of pure B embedded in an A-rich matrix phase, a. The concentration of B atoms in the vicinity of each /0-phase particle has an equilibrium value that increases with decreasing particle radius, as demonstrated in Fig. 15.1. Because of concentration differences, a flux of B atoms from smaller to larger particles develops in the matrix. This flux causes the smaller particles to shrink and the larger particles to grow. [Pg.364]

Pervaporation is a concentration-driven membrane process for liquid feeds. It is based on selective sorption of feed compounds into the membrane phase, as a result of differences in membrane-solvent compatibility, often referred to as solubility in the membrane matrix. The concentration difference (or, in fact, the difference in chemical potential) is obtained by applying a vacuum at the permeate side, so that transport through the membrane matrix occurs by diffusion in a transition from liquid to vapor conditions (Figure 3.1). Alternatively, a sweep gas can be used to obtain low vapor pressures at the permeate side with the same effect of a chemical potential gradient. [Pg.46]

Figure 16 The PL spectra of anthracene (A) 10-substituted with a long molecular thread (ANTPEP 10-[3,5-di(terbutyl)phenoxy]decyl-2-( 2-[(9-anthrylcarbonyl)amino] acetate)) in a bisphenol A polycarbonate (PC) matrix at different concentrations shown in the figure. The PL spectrum in the dilute solution of dichloromethane (DCM) is displayed for comparison (curve 4). Molecular structures of the chemical compounds are shown in the upper part of the figure. Adapted from Ref. 94. Figure 16 The PL spectra of anthracene (A) 10-substituted with a long molecular thread (ANTPEP 10-[3,5-di(terbutyl)phenoxy]decyl-2-( 2-[(9-anthrylcarbonyl)amino] acetate)) in a bisphenol A polycarbonate (PC) matrix at different concentrations shown in the figure. The PL spectrum in the dilute solution of dichloromethane (DCM) is displayed for comparison (curve 4). Molecular structures of the chemical compounds are shown in the upper part of the figure. Adapted from Ref. 94.
Equations (6.299) and (6.300) show that Onsager s reciprocal rules hold. The Js eq and Jweq have a microscopic definition represented by perturbation matrix elements and a macroscopic definition represented by the equilibrium exchange rate. As long as the criteria of linearization are satisfied, the statistical rate theory may be used to describe systems with temperature differences at an interface besides the driving forces of pressure and concentration differences. [Pg.355]

The Initial phase of the development was the determination of the relative solubility of the selected pheromone, ZZ and ZE-7, 11-hexadecadlenyl acetate (Gossyplure, 1 1 ratio). In a suitable polymer matrix. Four different water-soluble or water-reducible resins were Initially Investigated a water-soluble acrylic mixture, two latex emulsions and a natural rubber colloid. Intrln- sic solubility was determined by making resln/pheromone solutions of varying concentrations and measuring the rate of pheromone diffusion from dried films. In this manner, we were able to determine the most suitable base polymer from which to begin. [Pg.154]

Fig. 10. (a) Time-integrated emission spectrum and (b) PMDR (phosphorescence microwave double resonance) spectrum of Pd(2-thpy)2 at T = 1.4 K dissolved in an n-octane Shpol skii matrix. Concentration = 10 mol/1. Aexc = 330 nm. The PMDR spectrum is induced by a microwave irradiation with a frequency of 2886 MHz, which is in resonance with the energy difference between the triplet substates I and III. An intensity increase (+) signifies vibrational satellites that belong to an emission from the short-lived substate III, while a decrease (-) characterizes satellites of the emission spectrum from the long-lived substate I (Compare Ref. [61])... [Pg.113]

An intrinsic ionic charge gradient across the membrane exists because of semipermeable nature of membrane, which maintains a difference in the concentration of the ions between the cytosol and the extracellular matrix. This difference results in a definite potential across membrane of the normal cells, which is called the resting potential. Normal plant cells, mammalian muscle cells, and neurons have resting potential values of about —120, —90, and —70 mV, respectively. Along with the resistance to the flow of ions, membrane also exhibits a capacitance. Cm, which is given by... [Pg.746]

In the percolation of a liquid through a bed of solids, mass transfer of the solute from the surfaces of the solid to the liquid in the interstices of the bed takes place by molecular diffusion and by natural convection arising from the density changes created by dissolution. Although these processes are slow, they are much faster than mass transfer in the matrix under the same concentration differences. Concentration gradients in the liquid outside the particles are, therefore, very low. At any point in the bed, the introduction of dilute solution from above and the loss of concentrated solution to below decrease the interstitial concentration by dilution or displacement. This effect can be considered simply to reduce the solute concentration at the jimction of solid and solution, thus imposing a favorable concentration gradient within the matrix. [Pg.3904]

There are a number of different membrane techniques which have been suggested as alternatives to the SPE and LLE techniques. It is necessary to distinguish between porous and nonporous membranes, as they have different characteristics and fields of application. In porous membrane techniques, the liquids on each side of the membrane are physically connected through the pores. These membranes are used in Donnan dialysis to separate low-molecular-mass analytes from high-molecular-mass matrix components, leading to an efficient cleanup, but no discrimination between different small molecules. No enrichment of the small molecules is possible instead, the mass transfer process is a simple concentration difference over the membrane. Nonporous membranes are used for extraction techniques. [Pg.1408]

The elements of the first square matrix (dimensions nxn) are the differentials dcji / 3Q / = 1,2, - , n) of the stationary phase concentration of one sample component with respect to the mobile phase concentration of another sample component. Since in analytical chromatography all the sample components are present only at infinite dilution, differentiation of Eqs. 13.3 gives cross-partial differentials that are zero. Only the diagonal elements of this matrix are different from 0. These nonzero elements are equal to a,/(1 -I- EjhjCj) = so are simply related to... [Pg.613]

Equilibrium of adsorption on a solid is characterized by an adsorption isotherm, which shows the concentration on the solid as a function of the concentration in the contacting fluid. A quantitative measure of uptake of a gaseous species by a liquid is the distribution coefficient, defined as the ratio of the concentration on the solid to that in the contacting fluid. If concentration-independent, the coefficient is also called Henry coefficient. Diffusion of a species in a porous solid is expressed in terms of an effective diffusion coefficient, whose value accounts for the retardation by the solid matrix. Mass transfer to or from a solid is expressed in terms of a mass-transfer coefficient, the flux being the product of that coefficient and a concentration difference as "driving force."... [Pg.16]

The Antibody Dilution Matrix (after Hoffman et al 2008) is needed to determine the correct dilution of antibodies. For a different detection method, the matrix is the same, but the dilutions of the H antibody and other reagents may be a different antibody Dilution Matrix has different concentration ranges for different detection systems. To test the antibody Dilution Matrix with indirect fluorescent immunocy-tochemistry, run a preliminary experiment that uses eight samples. The results of this preliminary experiment will show the dilutions for both the D antibody and the 2° antibody. This one experiment will save so much time that its importance cannot overemphasized. [Pg.102]

In principle, by using an SPR apparatus with a G-rich strand attached to the matrix and different strand concentrations of the complementary oligonucleotide in solution, one can determine the k n and koff values for the intramolecular quadruplex and the bimolecular duplex. One of the major conclusions of these experiments is that both the folded and unfolded forms of the intramo-... [Pg.46]


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See also in sourсe #XX -- [ Pg.301 ]




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Concentration difference

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