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Logarithms rules

Taking the negative logarithm of both sides of the equation and manipulating logarithm rules yields cin equation called the Henderson-Hasselbalch equation, which relates the pH cind the pAT ... [Pg.241]

With logarithm rules, you can manipulate this equation to get j—y be more useful in certain situations. L J... [Pg.242]

Remember the logarithm rules in Appendix A.2, if you are not sure how this calculation works.)... [Pg.731]

Useful logarithm rules logxy = logx + logy logx/y = logx- logy log x = y log X... [Pg.190]

The volume coefficients of thermal expansion of the composite, polymer, and filler are a, i, and 2 respectively. The bulk moduli of the components are Bi and B2, respectively. The parameter G is the shear modulus of the polymer. The more the filler particles deviate from spherical, the greater the divergence of the thermal expansion coefficient from this equation. In such cases, the Thomas equation (41), or the logarithmic rule of mixtiu es, provides a better estimate. [Pg.3139]

Napier John (1550-1617) Scot, math., best known inventor of logarithm, originator of Napier s rules of eircular parts for solution of spherieal triangles and also Napier s bones (antecedent of a logarithmic rule) Nernst Hermann Walther (1864—1941)... [Pg.464]

A common logarithm, in general, consists of an integer, which is called the characteristic, and a decimal (usually endless), which is called the mantissa. The characteristic of any number may be determined from the following rules ... [Pg.176]

For a sequenee of reaetion steps two more eoneepts will be used in kinetics, besides the previous rules for single reaetions. One is the steady-state approximation and the seeond is the rate limiting step eoneept. These two are in strict sense incompatible, yet assumption of both causes little error. Both were explained on Figure 6.1.1 Boudart (1968) credits Kenzi Tamaru with the graphical representation of reaction sequences. Here this will be used quantitatively on a logarithmic scale. [Pg.123]

The logarithmic mean temperature difference is defined when AT, A7, Consider the case where AT2 = ATj. The logarithmic temperature difference is obtained by applying I lTopital s rule as AT2 —> AT, giving... [Pg.696]

In the case of a rectangular cross-section, a variety of methods and corresponding measurement point locations exist." - Table 12.8 shows the required measuring points for the log-Tchebycheff rule, where the velocity distribution in the wall-connected elements is logarithmic and in the central elements polynomial. [Pg.1164]

For base-10 logarithms, the rules governing significant figures are as follows ... [Pg.646]

The rules for significant figures involving natural logarithms and inverse logarithms are somewhat more complex than those for base-10 logs. However, for simplicity we will assume that the rules listed above apply here as well. Thus... [Pg.647]

Because logarithms are exponents, the rules governing the use of exponents apply as well The rules that follow are valid for all types of logarithms, regardless of the base. We illustrate the rules with natural logarithms that is where you are most likely to use them in working with this text. [Pg.647]

The advent of reasonably priced hand-held calculators has replaced the use of both logarithms and slide-rules for statistical calculations. In addition to the... [Pg.133]

Potentiometric instrnments are nsed most often when analyzing harmful contaminants in the air at production sites or in cities. Electrodes, whose potential is, as a rule, a linear fnnction of the logarithm of concentration of the substance to be determined (by Nemst s law), are the sensing elements in snch instruments. Most potentiometric sensors are highly selective. [Pg.406]

These relationships are termed the Harned rules and have been verified experimentally up to high overall molality values (e.g. for a mixture of HC1 and KC1 up to 2 mol-kg-1). If this linear relationship between the logarithm of the activity coefficient of one electrolyte and the molality of the second electrolyte in a mixture with constant overall molality is not fulfilled, then a further term is added, including the square of the appropriate molality ... [Pg.54]

It should be emphasized that the deviations from the logarithmic correlation obey the normal distribution statistics, allowing one to apply convenient statistical procedures to analytical measurement results. As will be shown below, the logarithmic linear correlation rule was observed for all types of geo-chemical samples, i. e., snow, air, water, and soil. The correlation analysis of the elemental composition of melted-snow fractions showed with confidence level 95% that no significant discrepancy exists between the element composition within the correlation curves (see Table 1) and the corresponding variances are thus homogeneous for any two randomly chosen samples (i. e., points of the territory). [Pg.143]

If we take the logarithm of equation (4) and apply the rules of logs we obtain... [Pg.231]

Activity coefficients in concentrated solutions are often described using Harned s rule (l ). This rule states that for a ternary solution at constant total molality the logarithm of the activity coefficient of each electrolyte is proportional to the molality of the other electrolyte. The expressions for the activity coefficients are written ... [Pg.721]

Fig. 8.1 Variation of the activity (logarithmic scale) or galvanic cell voltage as a function of the composition (schematic). The plateaux indicate multi-phase regions in which the activity is fixed according to Gibbs phase rule. Fig. 8.1 Variation of the activity (logarithmic scale) or galvanic cell voltage as a function of the composition (schematic). The plateaux indicate multi-phase regions in which the activity is fixed according to Gibbs phase rule.
Raman and IR spectroscopies are complementary to each other because of their different selection rules. Raman scattering occurs when the electric field of light induces a dipole moment by changing the polarizability of the molecules. In Raman spectroscopy the intensity of a band is linearly related to the concentration of the species. IR spectroscopy, on the other hand, requires an intrinsic dipole moment to exist for charge with molecular vibration. The concentration of the absorbing species is proportional to the logarithm of the ratio of the incident and transmitted intensities in the latter technique. [Pg.22]


See other pages where Logarithms rules is mentioned: [Pg.109]    [Pg.226]    [Pg.534]    [Pg.161]    [Pg.14]    [Pg.109]    [Pg.226]    [Pg.534]    [Pg.161]    [Pg.14]    [Pg.415]    [Pg.646]    [Pg.168]    [Pg.275]    [Pg.911]    [Pg.53]    [Pg.177]    [Pg.69]    [Pg.396]    [Pg.57]    [Pg.102]    [Pg.96]    [Pg.14]    [Pg.380]    [Pg.380]    [Pg.250]    [Pg.7]    [Pg.88]    [Pg.191]    [Pg.52]    [Pg.100]    [Pg.98]   
See also in sourсe #XX -- [ Pg.7 ]

See also in sourсe #XX -- [ Pg.156 ]




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