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Addition accuracy

Accuracy The accuracy of a fluorescence method is generally 1-5% when spectral and chemical interferences are insignificant. Accuracy is limited by the same types of problems affecting other spectroscopic methods. In addition, accuracy is affected by interferences influencing the fluorescent quantum yield. The accuracy of phosphorescence is somewhat greater than that for fluorescence. [Pg.432]

The//(tissue) values are averaged for the species, this average is assumed to be the value for human, inserted back into the Oie-Tozer equation and combined with the measured value of /,(piasma) in human to obtain a predicted value for human VD. However, despite its increased complexity it does not offer additional accuracy over the above mentioned dog-human proportionality method and may only be most appropriate when plasma protein binding shows considerable inter-species variability. [Pg.211]

When base selection and proofreading are combined, DNA polymerase leaves behind one net error for every 106 to 108 bases added. Yet the measured accuracy of replication in E. coli is higher still. The additional accuracy is provided by a separate enzyme system that repairs the mismatched base pairs remaining after replication. We describe this mismatch repair, along with other DNA repair processes, in Section 25.2. [Pg.955]

If additional accuracy is desired (on the order of 0.5 cm-1), then indene may be used (20). Indene also has been used as a frequency calibrant for IR spectrophotometers. Before use, it should be purified by vacuum distillation and stored in sealed capillary or an NMR tube. Figure 2-13 shows the Raman spectrum of indene, and Table 2-7 lists the frequencies that are recommended for use in calibration. [Pg.118]

NaCl solution. In one set of experiments, the slurry was titrated with 0.1 normal NaOH solution in one cm increments to a pH of about 10. The samples of this set are referred to as the "slurry" samples (titration of the calcined zeolite - NaCl solution slurry). In another set of experiments, the calcined zeolite - NaCl solution slurry was filtered, the filter cake washed with about 100 cnP distilled water, and the combined filtrates were titrated with 0.1 N NaOH solution, again to a pH of about 10. The samples of this latter set are referred to as the "filtrate" samples (the zeolite being removed by filtration prior to titration of the filtrate). In addition to the manual titrations, automated potentiometric titration curves were obtained with a Metrohm E636 Titroprocessor, which has an estimated pH measurement accuracy of 0.001 pH unit and an estimated volumetric addition accuracy of 0.001 cm ... [Pg.373]

For a system of coupled 7=1/2 nuclei, the transition frequencies in the multiple quantum spectra are determined by the dipolar coupling constants, the scalar coupling constants and the chemical shifts of the nuclei. In theory, the spectra of order N— 1 and N—2 contain sufficient transitions to measure all of the dipolar coupling constants and chemical shifts in an 7V-spin system. For additional accuracy and confidence, the A— 3 quantum spectrum can also be analysed to provide redundancy and more reliable estimates of the Dy. [Pg.4]

This representation is normally not needed for organic structures of a reasonable input quality with small distortions and the difference between the two functions is then negligible. A harmonic potential or a higher-order derivative of such is normally used in the initial optimization phase. Additional accuracy gained from a well-determined Morse function, at the cost of increase in complexity, may be important when studying more complex systems. [Pg.3]

As a preliminary test of the accuracy and precision of the complete method as recommended, a crude oil, that was found to contain less than 10 ng/g of cadmium when tested by the method, was spiked with 26 ng/g of cadmium and analyzed 10 times. The mean recovery was 28 ng/g, with a standard deviation of 6 ng/g. As in the case of the wet ash-flame method, additional accuracy and precision data were obtained by cross-checks in three different laboratories (14). The results, also consolidated in Table 7.1 V, confirmed the validity of the method. [Pg.95]

While considering tendons and ligaments as simple nonlinear elastic elements (Table 48.6) are often sufficient, additional accuracy can be obtained by incorporating viscous damping. The quasi-hnear viscoelastic approach [Fung, 1981] introduces a stress relaxation function, G(t), that depends only on time, is convoluted with the elastic response, T (A,), that depends only on the stretch ratio, to yield the complete stress response, K X, t). To obtain the stress at any point in time requires that the contribution of all preceding deformations be assessed ... [Pg.826]

While negative ion mode is vay usefid to identify known compounds, the first-order mass spectrum yielded by positive ion mode can provide more structural information. So, the combined use of both ionization modes can give additional accuracy to the molecular mass determination, which is particularly relevant when noise levels are high. "... [Pg.1773]

Upper error bounds can be foimd easily by approximating the sums with integrals (see [54]). As for the Lekner sum, the additional accuracy has to be paid for with only a small decrease of computational performance therefore, MMM is the method of choice if high accuracy is required. [Pg.82]

In routine blood analysis of electrolytes, where ISEs are used nearly universally, sometimes extremely small concentration changes are assessed with direct poten-tiometry. This requires potential stabilities and reproducibilities in the 10 to 100 microvolt range, which is achieved in temperature-controlled flow-through cells and with frequent, automated recalibrations between measurements. In batch mode benchtop analyses with ISEs, such a high precision is often not observed. In addition, accuracies are mainly limited by variations in the liquid junction potential between the calibration and sample phases and by interferences from other sample ions, temperature fluctuations, and if concentrations rather than activities are desired, variations in activity coefficients. The latter reflects the well-known relationship between the sample activity ai and its concentration c ... [Pg.5578]

Truncation error results from using a function like a polynomial to approximate the true solution. To reduce tmncation error, we could use more sophisticated functions—for example, higher order polynomials—which require more information. Multistep methods do this, but the additional accuracy gained by increasing the order of the method drops off very quickly beyond about k = 4. [Pg.145]

Most samples show more than one point of inflection. To avoid errors arising from this source, two determinations are done on different amounts of sample, and the difference between them is used to calculate the result. A blank titration is necessary for each determination. This means doing four titrations for each determination, which makes the method rather cumbersome. The analyst must decide in individual cases, on the basis of experience, whether the additional accuracy gained is sufficient to justify the three titrations of steps 4 and 5. [Pg.185]

The above method ass imes an infinite heat transfer coefficient on the fluid side of the concentrated mass, and hence tends to overestimate the percentage cooldown. Additional accuracy might be obtained if the method of calculation were refined to account for finite heat transfer coefficients. A refinement of this type might be helpful in those situations in which the heat input from the partial cooldown of concentrated masses is large in comparison with the heat input from the complete cooldown of the distributed mass. However, it is felt that for most conventional cryogenic transfer lines the assumption of an infinite coefficient is adequate to obtain a reasonable approximation of cooldown mass. [Pg.388]

If a check must be made, it must be completely independent. Rather than review a calculation, the calculation must be repeated independently and then compared. If we wanted to really improve the accuracy of orders through checking, we would have two people enter them independently and then compare them. If identical, they would go to the supplier for processing. If they differed, we would find and correct the problem. In the case of promotional products, this is too expensive for the additional accuracy we would achieve. We acknowledge that there are many circumstances in industry where this is necessary. However, in practice, we rarely see inspection carried out in this fashion. What we see is checking, reviewing the calculation made by another worker. This is the worst thing that could be done it will make accuracy worse, not better, and will cost time that could be better spent in other ways. [Pg.5]

A reliable and u.ser-friendly method for evaluating An for V-shaped levers deserves particular attention. Equation (17) con.stitutes the lowest-order approximation for purposes of modeling An. The expression has been used in several studies with various degrees of success (e.g., [40]), Two correction factors have been derived [46], which offer additional accuracy without unnecessarily adding complexity to the treatment. Application of the first factor to the lowest-order approximation, Eq. (17), results in... [Pg.428]

For diatomic molecules, it is often sufficiently accurate to describe the interaction by using a Morse potential. This has also been explicitly assumed in some of the previous sections. However, near the dissociation limit additional accuracy can be obtained by using a functional form containing additional parameters. Such a function is the extended Rydberg (ER) function, given by... [Pg.75]


See other pages where Addition accuracy is mentioned: [Pg.152]    [Pg.43]    [Pg.28]    [Pg.88]    [Pg.133]    [Pg.719]    [Pg.800]    [Pg.265]    [Pg.139]    [Pg.22]    [Pg.625]    [Pg.134]    [Pg.45]    [Pg.918]    [Pg.22]    [Pg.515]    [Pg.81]    [Pg.93]    [Pg.140]    [Pg.239]    [Pg.307]    [Pg.183]    [Pg.442]    [Pg.155]    [Pg.849]    [Pg.45]   
See also in sourсe #XX -- [ Pg.481 ]




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