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Total steady state

The element exists as an intermediate in uranium and thorium minerals through their decay. There is no stable isotope. The longest-living isotope has a half-life of 8.3 hours. In the crust of the Earth, the total steady-state mass is estimated at a few tens of grams. Thus astatine is the rarest element (record ). A few atoms of this relative of iodine can be found in all uranium ore. It exhibits certain metallic properties. [Pg.153]

It is very difficult to excite the donor without also exciting some of the acceptor population. This is because the absorption spectra of dyes extend significantly into the blue side of their absorption maxima, so the absorption spectra of the donor and acceptor usually overlap. The donor fluorescence can typically be observed without acceptor fluorescence interference therefore, when measuring FRET efficiency by observing the donor fluorescence, this overlap is not important. However, when observing the acceptor fluorescence the overlap of the donor and acceptor absorption must be taken into account. The total steady-state fluorescence of the acceptor, assuming that [A] = [D (i.e., a equal donor and acceptor concentrations, and 100% labeling) is... [Pg.57]

To develop E(B) for two CSTRs in series, we use a slightly different, but equivalent, method from that used for a single CSTR in Section 13.4.1.1. Thus, consider a small amount (moles) of tracer M, nMo = F,dt, where Ft is the total steady-state molar flow rate, added to the first vessel at time 0. The initial concentration of M is cMo = nMo/(V/2). We develop a material balance for M around each tank to determine the time-dependent outlet concentration of M from the second vessel, cM2(l). [Pg.411]

Note that the fractional intensity of component i, i.e. the fractional contribution of component i to the total steady-state intensity is... [Pg.172]

This means that the total steady-state protomer concentration, C , includes the amount necessary to equilibrate the polymers with Tb GTP (i.e., C°) plus the amount sequestered in the inactive form of Tb GDP. If the nucleotide dissociation constants, gdf and gtp> are known, then [Tb GDP] is determined. [Pg.189]

Given the PCBs inputs, 7t, and the atmospheric concentrations, Ca, we can now calculate the total steady-state concentration in the lake for the two congeners from Eq. 5 of Box 23.1. Note that among the input processes (nominator of Eq. 5) only the input from the rivers and the atmosphere are different from zero, whereas among the removal processes (denominator of Eq. 5) flushing, air/water exchange, and sedimentation are relevant. Thus, we can formulate the steady-state explicitly for the case of the two PCB congeners ... [Pg.1067]

Muraour and Ertand (Ref 29) exposed several primary expls in the atomic pile Zoe at Chatellon, France. Pb azide, MF, diazo meta mtraniline perchlorate, Pb trinitroresorcinate, and tetracene were subjected to total steady-state thermal neutron fluxes up to 1013 neutrons/cm2. The y component was not given. No explns were obtained with any of the materials during irradiation. The only effect noticed was a slight color change from white to light brown in tetracene. [Pg.34]

The use of microelectrodes under total steady-state conditions is very advantageous in determining kinetic constants of very fast chemical reactions. To show this, in Fig. 3.28, we show the time influence at different values of rs on the normalized limiting current of a CE mechanism (Eq. 3.249) compared with the time-independent solution (dashed lines and Eq. (3.250)) ... [Pg.214]

Equation (9,86), and the equivalent expression (with r replaced by / everywhere) for I Cl 12 = IC/ P give the steady-state population of individual levels, r and I, in the continua. This steady state was obtained by assigning to each such level a decay rate r). Therefore, the total steady-state flux out ofthe system through the continumn (channel) R is, in analogy to (9.71)... [Pg.333]

Figure 3.14 shows the total steady-state fuel-cycle cost for an interval of 1.0 year between refuelings as a function of feed enrichment for batch fractions, /, of 5, j, and j. The batch fraction is defined as 1 In, where n is the number of fuel zones. Also plotted in this flgure are levels of constant energy production (E) or capacity factor (/. ) and lines of constant burnup... [Pg.103]

The total steady-state flux through the pore can be determined by integration of Equation 5-12 ... [Pg.124]

Figure 14. Plot of the total steady-state reaction rate increase, r-s, -Vo, as a function of the anodic polarizing current, I. Reprinted from J. Ekctroanal. Chem., 0. F6ti, V. Stankovic, 1. Bolzonella, and Ch. Comninellis, Transient Behavior of Electrochemical Promotion of Gas-Phase Catalytic Reactions, (2002), in press, with permission from Elsevier Science. Figure 14. Plot of the total steady-state reaction rate increase, r-s, -Vo, as a function of the anodic polarizing current, I. Reprinted from J. Ekctroanal. Chem., 0. F6ti, V. Stankovic, 1. Bolzonella, and Ch. Comninellis, Transient Behavior of Electrochemical Promotion of Gas-Phase Catalytic Reactions, (2002), in press, with permission from Elsevier Science.
Figure 8. Plot of dimensionless total steady state bacterial density versus A/ for single randomly motile populations. Figure 8. Plot of dimensionless total steady state bacterial density versus A/ for single randomly motile populations.
Figure 9. Plot of dimensionless total steady state bacterial density vs. 8 for single chemotactic populations. Extrapoiations of perturbation computations beyond 8 — I shown (--------------). Asymptotic vaiues for S = 0 shown (------ -). Figure 9. Plot of dimensionless total steady state bacterial density vs. 8 for single chemotactic populations. Extrapoiations of perturbation computations beyond 8 — I shown (--------------). Asymptotic vaiues for S = 0 shown (------ -).
In scenario A (columns 2 and 3) of Table 16.5, where (as shown above) clearance is limited by hepatic plasma flow, a doubling of the fraction of dmg unbound in the plasma has minimal effect on total steady-state drug concentration but results in a near doubling of free steady-state dmg concentration. This increased free concentration will likely increase therapeutic or toxic effect and would require a downward adjustment in dose. [Pg.323]

Conversely, in scenario B (columns 4 and 5) Table 16.5, where clearance was limited by pCl inb a doubling of the fraction of dmg unbound in the plasma results in an almost perfectly inversely proportional change in total steady-state dmg concentration but has minimal effect on free steady-state dmg concentration. There would be virtually no potential for increased drug effect in this case however, a clinician monitoring the total dmg concentration could be alarmed by its decrease and order an inappropriate increase in the dose in order to increase the total drug concentration. [Pg.324]

We observe that an increase in free fraction of dmg causes an inversely proportional decrease in average total steady-state dmg concentration but no change in the corresponding free concentration. These changes are independent of the relative sizes of plasma flow to the liver and the volume of distribution of dmg in the body. [Pg.324]

In this expression, the 7 (2) are the individual emission spectra the/- ate the fractional contributions to the total steady-state intensity, s 1.0 and nij is the modulation of the ith component and is its phase angle. Dqtending upon the needs of the experiment, the steaify-state qwe-ttum of each species, can be replaced by the steady-... [Pg.620]

For mixed gas experiments, the flow rates and composition of the feed gas were controlled using electronic mass flow controllers. The total feed pressure was kept steady at 227.5 cm Hg (303 kPa) while the permeate pressure and temperature were maintained at ambient conditions (62 cm Hg and room temperature). Permeate and retentate streams, with helium as the sweep gas (on permeate side), were analyzed for gas compositions using a gas chromatograph (SRI Instruments, model 8610 C). The total steady state permeate flow rate and the gas composition of the permeate stream were used to calculate the analyte gas flux. From the flux, and the pressure differential across the membrane, the gas permeances and separation factor (ratio of permeance) can be calculated. [Pg.228]

Steady-state and time-resolved measurements are related. The steady-state concentration of excited-states of a lumophore of lifetime t is Rabs(t> where is the rate of absorption of photons, in E dm s (E is the Einstein, which corresponds to 1 mole of photons), and 4> the quantum yield for excited-state formation. The total steady-state emission intensity is where Trad is the... [Pg.479]

Note that the total steady-state recombination rate per unit volume is... [Pg.20]

There is no known frictional LAD channel loss data reported in the literature. Equations (3.23), (3.33), (3.57), and (3.58) can be substituted into Equation (3.2) for a given LAD system to determine the total steady state pressure drop for the LAD system for any configuration. ID model results are compared to 1-g inverted vertical outflow test results in LH2 in Chapter 9. [Pg.72]

The total steady-state rate of excitation also can be written as... [Pg.438]

Total steady state error was less than 1 percent relative to CCEP... [Pg.462]


See other pages where Total steady state is mentioned: [Pg.456]    [Pg.213]    [Pg.328]    [Pg.1982]    [Pg.2742]    [Pg.174]    [Pg.41]    [Pg.194]    [Pg.213]    [Pg.151]    [Pg.104]    [Pg.196]    [Pg.376]    [Pg.128]    [Pg.67]    [Pg.87]    [Pg.60]    [Pg.60]    [Pg.53]    [Pg.566]   
See also in sourсe #XX -- [ Pg.213 , Pg.214 , Pg.215 ]




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Total drug concentration at steady state

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