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Mean life time equation

In the present case, the intracrystalline mean life times should be compared with a value of Ti lrou ,f = 0,007 ms, which results from inserting the mean crystallite radius and the intracrystalline self-diffusion coefficient (- 10 nrs ) at the given temperature and concentration (15) into Equation 10. Since in the nmr measurement is found to be much less than 0.2 ms,... [Pg.384]

For a direct check of the existence or non-existence of surface barriers we have applied the nmr tracer desorption technique. For a few selected systems, Table I gives a comparison between the mtracrvstaiiine mean life times a,and the quantities T ,n., l J 1 calculated from the coefficients oi intra-crystalline diffusion on the basis of Equation 11. The order of - magnitude agreement between these quantities indicates that under the given conditions in fact a substantial influence of surface barriers on molecular transport may be excluded,... [Pg.384]

The local linear velocity of shrinkage is m, which depends upon time and position in the layers . Equation (10.16) is applied to the fine-scale vortices, because only there are the layers sufficiently thin for molecular diffusion to effect contact between A and B on the molecular scale (micromixing). The initial thickness of the layers is about A ( and the initial vortex diameter about 12Ak. Deformation is completed during the mean life-time of such a fine-scale vortex, T , where... [Pg.191]

The termination rate constants can be estimated in two ways. If conductivity measurements are available plus a reasonable value for then k. =X Ri l. Where X is the mean life time for the charge carriers and may be rigorously determined from the conductivity measurements. Alternatively kt can be calculated from the simplified Debye equation. [Pg.519]

In a number of experiments substrate temperature is kept to be so low, that mean life time of adatoms exceeds the time of maximum supersatmation formation (so-called regime of complete condensation). In this case one is to solve the condensation equation together with the non-stationary diffusion equation describing the growth of clusters. Taking to = oo gives the following bedance equation... [Pg.101]

From equation 8 it was shown that the chance of surviving the mean life was 36.8% for the exponential distribution. However, this fact must be used with some degree of rationaHty in appHcations. For example, in the above situation the longest surviving MPU that was observed survived for 291.9 hours. The failure rate beyond this time is not known. What was observed was only a failure rate of A = 1.732 x lO " failures per hour over approximately 292 hours of operation. In order to make predictions beyond this time, it must be assumed that the failure rate does not increase because of wearout and... [Pg.10]

The half-life of a reactant and the mean reaction time of a reaction are two measures of the time to reach equilibrium. The half-life ty2 is the time for the reactant to decrease to half of its initial concentration, or more generally, the time for it to decrease to halfway between the initial and the final equilibrium concentration. The mean reaction time t is roughly the time it takes for the reactant concentration to change from the initial value to 1/e toward the final (equilibrium) value. The rigorous definition of the mean reaction time t is through the following equation (Equation 1-60) ... [Pg.96]

In Figure 10.30 the survival rate of the total sedimentary mass for the different Phanerozoic systems is plotted and compared with survival rates for the total carbonate and dolomite mass distribution. The difference between the two latter survival rates for each system is the mass of limestone surviving per unit of time. Equation 10.1 is the log linear relationship for the total sedimentary mass, and implies a 130 million year half-life for the post-Devonian mass, and for a constant sediment mass with a constant probability of destruction, a mean sedimentation rate since post-Devonian time of about 100 x 1014 g y 1. The modem global erosional flux is 200 x 1014 g y-1, of which about 15% is particulate and dissolved carbonate. Although the data are less reliable for the survival rate of Phanerozoic carbonate sediments than for the total sedimentary mass, a best log linear fit to the post-Permian preserved mass of carbonate rocks is... [Pg.551]

Equation (58) indicates that an increase in initiatior concentration will not enhance the rate of polymerization. It can be used for estimating the molecular mass of the polymer assuming, of course, the absence of transfer. The ratio N/q corresponds to the mean time of polymer growth and molecular mass is equal to the product of the number of additions per unit time and the length of the active life time of the radical, kpN/e. An increase in [I] also means a higher value of q, and thus a shortening of the chains. As in Phase II, the polymerized monomer in the particles is supplemented by monomer diffusion from the droplets across the aqueous phase a stationary state is rapidly established with constant monomer concentration in the particle. The rate of polymerization is then independent of conversion (see, for example the conversion curves in Fig. 7). We assume that the Smith-Ewart theory does not hold for those polymerizations where the mentioned dependence is not linear [132], The valdity of the Smith-Ewart theory is limited by many other factors. [Pg.284]

Relevant kinetic parameters (half-life, body pool, and mean transit time in organs) can be calculated. According to Equation 1 the specific activity in plasma shows a triphasic decay with half-lives of ti = 1.1 h, t2 == 22 h, and 3 == 61 h. The half-lives ti and 2 essentially describe the distribution of the compound into the system. The third half-life of 61 h (2.5 d) is valid for all tissues after attainment of the distribution equilibrium and represents the overall half-life of elimination from the body under the special conditions of the study (ascorbate status of the animals). [Pg.309]

The characteristic life time of a reaction is a measure of the time required after initiation for it to reach completion. This period is frequently related to the rate constant for the reaction in a veiy clear and specific way. Solutions to some of the common zero-, first- and second-order rate equations are presented in Table 9.5. Examples of zero- and first-order reactions are discussed in this section application of the second-order equations to general catalytic processes will be presented in the section on catalysis. The last column of Table 9.5 lists the relations between r, the characteristic life time of the reactant with respect to the chemical reaction, and the rate constant for the reaction. The meaning of the characteristic life time depends upon the order and reversibility of the reaction. [Pg.319]

Here, is the correlation time for the molecular motion of the C—H vector, meaning the time (or the life time) in which the C—H vector stays in the same direction without any motion. Figure 3.5 shows Tj, T2 and NOE as functions of t, which are obtained using Equation (3.17). [Pg.57]

More recently, Benet has described so-called multiple dosing half-lives, the half-life for a drug that is equivalent to the dosing interval to choose so that plasma concentrations (Equation 17.31) or amounts of drug in the body (Equation 17.32) will show a 50% drop during a dosing interval at a steady state. These parameters are defined in terms of the mean residence time in the central compartment (MRTC)and the mean residence time in the body MRT). [Pg.644]

Based on damage data from the field, it is feasible, by means of statistical distribution models, to describe product failure in a statistically sound way. The state of the art in industry is the application of WeibuU distribution models (Pfeifer, T. 2002). Using the WeibuU distribution function Fwd(1), cf equation (1), and the WeibuU density functionywo(t)> cf- equation (2), it is feasible to form the failure rate function X(t), cf. equation (3). The parameters are to (failure-free time), T (characteristic life time) and b (form parameter). The use of WeibuU distribution models allows to describe simple product failures and to inden-tify different damage phases or behaviors in a product Ufe cycle (Birolini, A. 2007). [Pg.798]

The exponential integral Ei(x) is defined by Jahnke and Emde. If < = 0 taken to be a time shortly after birth, but long enough after birth to exclude infant deaths (which are omitted in Gompertz treatment), then mean life span from birth to death. If then T/td is a constant for all animal species, we find from equations (8) and (9) that A is a constant, independent of species, given by the solution of the equation... [Pg.488]

A practical use of fitting a distribution to reliability data is to extrapolate to smaller failure rates or other environmental conditions. To simplify the equations, the expressions in the text refer to the mean life of the relevant portion of the assembly. If the constants that define the failure distribution are known, the time to reach a smaller proportion of failures may be readily calculated. For example, for failure modes that are described by a Weibull distribution, the time f to reach x% failures is given by ... [Pg.1319]

Under isothermal conditions, these four equations are sufficient to describe the flow of water (or air and any other gas or liquid with so-called Newtonian behavior of the viscosity). However, in most cases of industrial interest (i.e., at large scale), these equations cannot be solved using analytical techniques. The momentum balance is nonlinear in velocity, which makes analytical solution virtually always impossible. This is reflected in the properties of the flow of water it is in many cases turbulent. This means that the flow is inherently transient in time a steady state solution only exists for the time-averaged flow. The real flow shows a wide variety of structures, both in time and in space the flow field is built up of eddies of all kinds of sizes that have a finite life time. They come and disappear. These eddies make the solution very difficult. However, they are also vital to the processes we are running they make flow so effective in transport and mixing. Without them, we would have to rely on diffusion, which is a very slow process, and life on a larger scale as we know it would not have been possible. [Pg.94]


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See also in sourсe #XX -- [ Pg.42 , Pg.131 , Pg.183 ]




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