Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

First fluxes

First flux estimates through larger parts of its metabolism were based on constraining assumed reaction networks with measurement of uptake and production rates [74]. A number of studies utilized stoichiometric balancing to assess the flexibility of the metabolic network [11, 75] and to investigate the influence of environmental conditions such as dissolved oxygen level [88], salt content [89], or nutrient status [12,90, 91]. However, this conventional approach cannot yield reliable information about parallel or bidirectional reactions and has to rely on balances for NADH or NADPH, which may not be accurate [34]. Moreover, it is limited to derive new conclusions since the results are strongly based on the taken assumptions and not on data [92],... [Pg.33]

The composition of talc corresponds to the position close to the lowest eutectic in the system Mg0-Si02(cf. Fig. 23). The first flux arises in the pure mineral at 1543 C. Below this temperature, metasilicate and cristobalite are the only equilibrium phases. [Pg.24]

Several different flux conserver shapes and external field conditions have been used to test the gross stability of the spheromak. Some of these configurations are shown in Fig, 6, As predicted by theory, the prolate spheromaks produced in the first flux conserver in Fig, 6 were unstable to the n = 1, m = 1 tilting mode (n and m are the toroidal and poloidal mode numbers), but the oblate shape of the other three conservers stabilized the tilt. The addition of external field has a destabilizing influence, but the last flux conserver shown stabilized the plasma even with significant external field. [Pg.468]

A SQUID [2] provides two basic advantages for measuring small variations in the magnetic field caused by cracks [3-7]. First, its unsurpassed field sensitivity is independent of frequency and thus dc and ac fields can be measured with an resolution of better than IpT/VHz. Secondly, the operation of the SQUID in a flux locked loop can provide a more than sufficient dynamic range of up to 160 dB/VHz in a shielded environment, and about 140 dB/>/Hz in unshielded environment [8]. [Pg.255]

There are two approaches to the kinetics of emulsion flocculation. The first stems from a relationship due to Smoluchowski [52] for the rate of diffusional encounters, or flux ... [Pg.511]

The exact quantum expression for the activated rate constant was first derived by Yamamoto [6]. The resulting quantum reactive flux correlation fiinction expression is given by... [Pg.891]

The RRKM rate constant is often expressed as an average classical flux tlirough the transition state [18,19 and 20]. To show that this is the case, first recall that the density of states p( ) for the reactant may be expressed as... [Pg.1014]

Diffusion may be defined as the movement of a species due to a concentration gradient, which seeks to maximize entropy by overcoming inhomogeneities within a system. The rate of diffusion of a species, the flux, at a given point in solution is dependent upon the concentration gradient at that particular point and was first described by Pick in 1855, who considered the simple case of linear difflision to a planar surface ... [Pg.1924]

If the molecules could be detected with 100% efficiency, the fluxes quoted above would lead to impressive detected signal levels. The first generation of reactive scattering experiments concentrated on reactions of alkali atoms, since surface ionization on a hot-wire detector is extremely efficient. Such detectors have been superseded by the universal mass spectrometer detector. For electron-bombardment ionization, the rate of fonnation of the molecular ions can be written as... [Pg.2062]

The diffusion of small molecules in polymers can be described using Pick s first and second laws. In a onedimensional situation, the flux J(c, x) as a function of the concentration c and the position x is given by... [Pg.2535]

At the present time there exist no flux relations wich a completely sound cheoretical basis, capable of describing transport in porous media over the whole range of pressures or pore sizes. All involve empiricism to a greater or less degree, or are based on a physically unrealistic representation of the structure of the porous medium. Existing models fall into two main classes in the first the medium is modeled as a network of interconnected capillaries, while in the second it is represented by an assembly of stationary obstacles dispersed in the gas on a molecular scale. The first type of model is closely related to the physical structure of the medium, but its development is hampered by the lack of a solution to the problem of transport in a capillary whose diameter is comparable to mean free path lengths in the gas mixture. The second type of model is more tenuously related to the real medium but more tractable theoretically. [Pg.3]

Clearly the general situation is very complicated, since all three mechanisms operate simultaneously and might be expected to interact in a complex manner. Indeed, this problem has never been solved rigorously, and the momentum transfer arguments we shall describe circumvent the difficulty by first considering three simple situations in which each of the three separate mechanisms in turn operates alone. In these circumstances Che relations between fluxes and composition and/or pressure gradients can be found without too much difficulty. Rules of combination, which are essea-... [Pg.7]

Equations (2.10), (2.18) and (2.24) provide the flux relations in situations where each of the three separate mechanisms of momentum transfer dominates. However, there remains the problem of finding the flux relations in "intermediate" situations where all three mechanisms may be of comparable importance. This has been discussed by Mason and Evans [7], who assumed first that the rates of momentum transfer due to mechanisms (i) and (ii) should be combined additively. If we write equation (2.10) in the form... [Pg.15]

Let us now turn attention to situations in which the flux equations can be replaced by simpler limiting forms. Consider first the limiting case of dilute solutions where one species, present in considerable excess, is regarded as a solvent and the remaining species as solutes. This is the simplest Limiting case, since it does not involve any examination of the relative behavior of the permeability and the bulk and Knudsen diffusion coefficients. [Pg.36]

In the first, motion is generated by composition gradients in the absence of any temperature or pressure gradient, in the second, motion is a consequence of pressure gradients alone, and in the third,both pressure and composition gradients are present but a constraint of zero net molar flux is imposed. These will be discussed in turn. [Pg.50]

Without assuming something specific about the reaction rate, it is not possible to go further and actually determine the micropore fluxes. We shall therefore consider the particular case of a first order reversible isomeri-... [Pg.82]

In simple cases it is not difficult to estimate the magnitude of the pressure variation within the pellet. Let us restrict attention to a reaction of the form A nB in a pellet of one of the three simple geometries, with uniform external conditions so that the flux relations (11.3) hold. Consider first the case in which all the pores are small and Knudsen diffusion controls, so that the fluxes are given by... [Pg.130]

Equations (12.13) and (12.14) may be approximated by rather simple equations in most conditions of physical interest. This is possible because of the relatively large value of the thermal conductivity of the solid matrix, which has two important consequences. First, the conductive enthalpy flux, represented by the second term on the left hand side of... [Pg.163]

Now in the present case i/a 1, so it follows from equation (A.1.7) that G/a 1, provided f differs significantly from zero. Thus che first term on the right hand side of (A.L.8) is a close approximation to the familiar Poisoiille flux. The second term, on the other hand, represents thermal transpiration. In particular, setting N 0, we find... [Pg.181]


See other pages where First fluxes is mentioned: [Pg.102]    [Pg.227]    [Pg.246]    [Pg.162]    [Pg.33]    [Pg.102]    [Pg.227]    [Pg.246]    [Pg.162]    [Pg.33]    [Pg.298]    [Pg.300]    [Pg.508]    [Pg.950]    [Pg.726]    [Pg.885]    [Pg.893]    [Pg.914]    [Pg.990]    [Pg.1243]    [Pg.1813]    [Pg.1926]    [Pg.2859]    [Pg.15]    [Pg.34]    [Pg.51]    [Pg.63]    [Pg.133]    [Pg.133]    [Pg.143]    [Pg.159]    [Pg.186]    [Pg.396]    [Pg.207]    [Pg.9]    [Pg.400]    [Pg.639]   
See also in sourсe #XX -- [ Pg.61 ]




SEARCH



First-order-reaction Fluxes

© 2024 chempedia.info