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Kinetics membranes

The theory of ion-selective electrode response is well developed, due to the works of Eisenman, Buck and others [23], Three models used for the description of the ISE response through the years, namely kinetic, membrane surface (or space charge) and phase boundary potential (PBP) models, although being seemingly contradictory, give similar results in most cases [7], The first two sophisticated models are out of the scope of the present chapter, as the PBP model, despite its simplicity, satisfactorily explains most of the experimental results and thus has become widely applicable. The... [Pg.101]

LIPID PHASE TRANSITION KINETICS Membrane lipid asymmetry,... [Pg.760]

Key Words Pulsed low electric fields Endocytosis Uptake kinetics Membrane internalization Albumin Lucifer Yellow Propidium iodide Adsorption Flow cytometry Confocal microscopy. [Pg.141]

Of the four redox centres, haem a is the most likely one to be coupled to proton translocation (Fig. 3.6). It exhibits heterogeneous oxidoreduction kinetics, membrane sidedness with respect to proton dependence, and looses the proton-dependence of oxidoreduction simultaneously with loss of proton pumping when subunit III is removed from the enzyme (see below, and discussion in Refs. 92, 99). [Pg.66]

Factors which influence the effectiveness of membrane separation systems are summarized. These factors include the complexation/decomplexation kinetics, membrane thickness, complex diffusivity, anion type, solvent type, and the use of ionic additives. [Pg.10]

The most important constitutive equations for the reaction kinetics, membrane flux are described above while axial and radial dispersion coefficients are discussed in Section 10.5. The main equations read ... [Pg.13]

Kinetic Membrane - bound ApoHBD (control or diabetic)... [Pg.214]

Liquid membrane separation systems possess great potential for performing cation separations. Many factors influence the effectiveness of a membrane separation system including complexation/ decomplexation kinetics, membrane thickness, complex diffusivity, anion type, solvent type, and the use of ionic additives. The role that each of these factors plays in determining cation selectivity and flux is discussed. In an effort to arrive at a more rational approach to liquid membrane design, the effect of varying each of these parameters is established both empirically and with theoretical models. Finally, several general liquid membrane types are reviewed, and a novel membrane type, the polymeric inclusion membrane, is discussed. [Pg.57]

As discussed above, the temperature can influence the OCV of a PEM fuel cell and thermodynamics, electrode kinetics, membrane conductivity, hydrogen crossover, and mass transfer process, and this influence will be reflected in the overall cell performance. However, the dependence of performance on temperature can be complicated by the fact that other conditions, such as RH, backpressure, gas stochiometry, flow field design, and electrode structure, also affect performance. [Pg.143]

Mixtures of trioctylamine and 2-ethylhexanol have been employed to extract 1—9% by volume acetic acid from its aqueous solutions. Reverse osmosis for acid separation has been patented and solvent membranes for concentrating acetic acid have been described (58,59). Decalin and trioctylphosphine were selected as solvents (60). Liquid—Uquid interfacial kinetics is an especially significant factor in such extractions (61). [Pg.69]

For example, the measurements of solution osmotic pressure made with membranes by Traube and Pfeffer were used by van t Hoff in 1887 to develop his limit law, which explains the behavior of ideal dilute solutions. This work led direcdy to the van t Hoff equation. At about the same time, the concept of a perfectly selective semipermeable membrane was used by MaxweU and others in developing the kinetic theory of gases. [Pg.60]

A crystalline or semicrystalline state in polymers can be induced by thermal changes from a melt or from a glass, by strain, by organic vapors, or by Hquid solvents (40). Polymer crystallization can also be induced by compressed (or supercritical) gases, such as CO2 (41). The plasticization of a polymer by CO2 can increase the polymer segmental motions so that crystallization is kinetically possible. Because the amount of gas (or fluid) sorbed into the polymer is a dkect function of the pressure, the rate and extent of crystallization may be controUed by controlling the supercritical fluid pressure. As a result of this abiHty to induce crystallization, a history effect may be introduced into polymers. This can be an important consideration for polymer processing and gas permeation membranes. [Pg.223]

Advantages to Membrane Separation This subsertion covers the commercially important membrane applications. AU except electrodialysis are pressure driven. All except pervaporation involve no phase change. All tend to be inherently low-energy consumers in the-oiy if not in practice. They operate by a different mechanism than do other separation methods, so they have a unique profile of strengths and weaknesses. In some cases they provide unusual sharpness of separation, but in most cases they perform a separation at lower cost, provide more valuable products, and do so with fewer undesirable side effects than older separations methods. The membrane interposes a new phase between feed and product. It controls the transfer of mass between feed and product. It is a kinetic, not an equihbrium process. In a separation, a membrane will be selective because it passes some components much more rapidly than others. Many membranes are veiy selective. Membrane separations are often simpler than the alternatives. [Pg.2024]

Process Description Reverse osmosis (RO) and nanofiltration (NF) processes utilize a membrane that selectively restricts flow of solutes while permitting flow of the solvent. The processes are closely related, and NF is sometimes called loose RO. They are kinetic processes, not equilibrium processes. The solvent is almost always water. [Pg.2034]

Salt flux across a membrane is due to effects coupled to water transport, usually negligible, and diffusion across the membrane. Eq. (22-60) describes the basic diffusion equation for solute passage. It is independent of pressure, so as AP — AH 0, rejection 0. This important factor is due to the kinetic nature of the separation. Salt passage through the membrane is concentration dependent. Water passage is dependent on P — H. Therefore, when the membrane is operating near the osmotic pressure of the feed, the salt passage is not diluted by much permeate water. [Pg.2035]

The more permeable component is called the. st ga.s, so it is the one enriched in the permeate stream. Permeability through polymers is the product of solubihty and diffusivity. The diffusivity of a gas in a membrane is inversely proportional to its kinetic diameter, a value determined from zeolite cage exclusion data (see Table 22-23 after Breck, Zeolite Molecular Sieves, Wiley, NY, 1974, p. 636). [Pg.2047]

Advanced Materials Experimental membranes have shown remarkable separations between gas pairs such as O9/N9 whose kinetic dian ieters (see Table 22-23) are quite close. Most prominent is the carbon molecular sieve membrane, which operates by ultran iicro-porous molecular sieving (see Fig. 22-48c). Preparation of large-scale permeators based on ultran iicroporous membranes has proven to be a major challenge. [Pg.2050]

From a thermodynamic and kinetic perspective, there are only three types of membrane transport processes passive diffusion, faeilitated diffusion, and active transport. To be thoroughly appreciated, membrane transport phenomena must be considered in terms of thermodynamics. Some of the important kinetic considerations also will be discussed. [Pg.297]

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]

In this chapter we will provide an overview of the application of membrane separations for chiral resolutions. As we will focus on physical separations, the use of membranes in kinetic (bio)resolutions will not be discussed. This chapter is intended to provide an impression, though not exhaustive, of the status of the development of membrane processes for chiral separations. The different options will be discussed on the basis of their applicability on a large scale. [Pg.128]

A consequence of this theoretical approach which includes kinetic parameters is the establishment and coupling of certain ion fluxes across the phase boundary (equality of the sum of cathodic and anodic partial currents leading to a mixed potential). If a similar approach can be applied to asymmetric biological membranes with different thermodynamic equilibrium situations at both surfaces, the active ion transport could also be understood. [Pg.219]

Otherwise it has been shown that the accumulation of electrolytes by many cells runs at the expense of cellular energy and is in no sense an equilibrium condition 113) and that the use of equilibrium thermodynamic equations (e.g., the Nemst-equation) is not allowed in systems with appreciable leaks which indicate a kinetic steady-state 114). In addition, a superposition of partial current-voltage curves was used to explain the excitability of biological membranes112 . In interdisciplinary research the adaptation of a successful theory developed in a neighboring discipline may be beneficial, thus an attempt will be made here, to use the mixed potential model for ion-selective membranes also in the context of biomembrane surfaces. [Pg.237]


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See also in sourсe #XX -- [ Pg.57 , Pg.58 , Pg.58 ]




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