Titrations titration curves

Acid-base titrations - titration curves for strong and weak acids and bases... 

Albery W J and Brett C M A 1983 The wall-]et ring disc electrode. 2. Collection efficiency, titration curves and anodic stripping voltammetry J. Electroanal. Chem. 148 201... 

Tanford, C., Kirkwood, J. G. Theory of protein titration curves. I. General equations for impenetrable spheres. J. Am. Chem. Soc. 79 (1957) 5333-5339. 6. Garrett, A. J. M., Poladian, L. Refined derivation, exact solutions, and singular limits of the Poisson-Boltzmann equation. Ann. Phys. 188 (1988) 386-435. Sharp, K. A., Honig, B. Electrostatic interactions in macromolecules. Theory and applications. Ann. Rev. Biophys. Chem. 19 (1990) 301-332. 

Bashford, D., Karplus, M. Multiple-site titration curves of proteins an analysis of exact and approximate methods for their calculation. J. Phys. Chem. 95 (1991) 9556-9561. 

Tanford, C., Roxby, R. Interpretation of protein titration curves Application to lysozyme. Biochem. 11 (1972) 2192-2198. 

FIGURE 27 2 The titration curve of glycine At pH values less than pKs H3NCH2CO2H is the major species present At pH values between pKs and pK z the principal species is the zwitter... 

A selected list of redox indicators will be found in Table 8.26. A redox indicator should be selected so that its if" is approximately equal to the electrode potential at the equivalent point, or so that the color change will occur at an appropriate part of the titration curve. If n is the number of electrons involved in the transition from the reduced to the oxidized form of the indicator, the range in which the color change occurs is approximately given by if" 0.06/n volt (V) for a two-color indicator whose forms are equally intensely colored. Since hydrogen ions are involved in the redox equilibria of many indicators, it must be recognized that the color change interval of such an indicator will vary with pH. 

The titration curve in Figure 9.1 is not unique to an acid-base titration. Any titration curve that follows the change in concentration of a species in the titration reaction (plotted logarithmically) as a function of the volume of titrant has the same general sigmoidal shape. Several additional examples are shown in Figure 9.2. 

Concentration is not the only property that may be used to construct a titration curve. Other parameters, such as temperature or the absorbance of light, may be used if they show a significant change in value at the equivalence point. Many titration reactions, for example, are exothermic. As the titrant and analyte react, the temperature of the system steadily increases. Once the titration is complete, further additions of titrant do not produce as exothermic a response, and the change in temperature levels off. A typical titration curve of temperature versus volume of titrant is shown in Figure 9.3. The titration curve contains two linear segments, the intersection of which marks the equivalence point. 

Examples of titration curves for (a) a complexation titration, (b) a redox titration, and (c) a precipitation titration. 

In the overview to this chapter we noted that the experimentally determined end point should coincide with the titration s equivalence point. For an acid-base titration, the equivalence point is characterized by a pH level that is a function of the acid-base strengths and concentrations of the analyte and titrant. The pH at the end point, however, may or may not correspond to the pH at the equivalence point. To understand the relationship between end points and equivalence points we must know how the pH changes during a titration. In this section we will learn how to construct titration curves for several important types of acid-base titrations. Our... 

Titrating Strong Acids and Strong Bases For our first titration curve let s consider the titration of 50.0 mb of 0.100 M HCl with 0.200 M NaOH. For the reaction of a strong base with a strong acid the only equilibrium reaction of importance is... 

The first task in constructing the titration curve is to calculate the volume of NaOIi needed to reach the equivalence point. At the equivalence point we know from reaction 9.1 that... 

The approach that we have worked out for the titration of a monoprotic weak acid with a strong base can be extended to reactions involving multiprotic acids or bases and mixtures of acids or bases. As the complexity of the titration increases, however, the necessary calculations become more time-consuming. Not surprisingly, a variety of algebraic and computer spreadsheet approaches have been described to aid in constructing titration curves. 

Sketching an Acid—Base Titration Curve To evaluate the relationship between an equivalence point and an end point, we only need to construct a reasonable approximation to the titration curve. In this section we demonstrate a simple method for sketching any acid-base titration curve. Our goal is to sketch the titration curve quickly, using as few calculations as possible. 

Sketch the titration curve for the titration of 50.0 mb of 0.100 M acetic acid with 0.100 M NaOH. This is the same titration for which we previously calculated the titration curve (Table 9.3 and Figure 9.6). 

We begin by drawing the axes for the titration curve (Figure 9.7a). We have already shown that the volume of NaOH needed to reach the equivalence point is 50 mb, so we draw a vertical line intersecting the x-axis at this volume (Figure 9.7b). 

How to sketch an add-base titration curve see text for explanation. 

This approach can be used to sketch titration curves for other acid-base titrations including those involving polyprotic weak acids and bases or mixtures of weak acids and bases (Figure 9.8). Figure 9.8a, for example, shows the titration curve when titrating a diprotic weak acid, H2A, with a strong base. Since the analyte is... 

Figure 9.8b shows a titration curve for a mixture consisting of two weak acids HA and HB. Again, there are two equivalence points. In this case, however, the equivalence points do not require the same volume of titrant because the concentration of HA is greater than that for HB. Since HA is the stronger of the two weak acids, it reacts first thus, the pH before the first equivalence point is controlled by the HA/A buffer. Between the two equivalence points the pH reflects the titration of HB and is determined by the HB/B buffer. Finally, after the second equivalence point, the excess strong base titrant is responsible for the pH. 

Where Is the Equivalence Point We have already learned how to calculate the equivalence point for the titration of a strong acid with a strong base, and for the titration of a weak acid with a strong base. We also have learned to sketch a titration curve with a minimum of calculations. Can we also locate the equivalence point without performing any calculations The answer, as you may have guessed, is often yes ... 

It has been shown that for most acid-base titrations the inflection point, which corresponds to the greatest slope in the titration curve, very nearly coincides with the equivalence point. The inflection point actually precedes the equivalence point, with the error approaching 0.1% for weak acids or weak bases with dissociation constants smaller than 10 , or for very dilute solutions. Equivalence points determined in this fashion are indicated on the titration curves in figure 9.8. 

The principal limitation to using a titration curve to locate the equivalence point is that an inflection point must be present. Sometimes, however, an inflection point may be missing or difficult to detect, figure 9.9, for example, demonstrates the influence of the acid dissociation constant, iQ, on the titration curve for a weak acid with a strong base titrant. The inflection point is visible, even if barely so, for acid dissociation constants larger than 10 , but is missing when is 10 k... 

Titration curve for 50.00 ml of 0.100 M CH3COOH with 0.100 M NaOH showing the range of pHs and volumes of titrant over which the indicators bromothymol blue and phenolphthalein are expected to change color. 

The need for the indicator s color transition to occur in the sharply rising portion of the titration curve justifies our earlier statement that not every equivalence point has an end point. For example, trying to use a visual indicator to find the first equivalence point in the titration of succinic acid (see Figure 9.10c) is pointless since any difference between the equivalence point and the end point leads to a large titration error. 

The most obvious sensor for an acid-base titration is a pH electrode.For example, Table 9.5 lists values for the pH and volume of titrant obtained during the titration of a weak acid with NaOH. The resulting titration curve, which is called a potentiometric titration curve, is shown in Figure 9.13a. The simplest method for finding the end point is to visually locate the inflection point of the titration curve. This is also the least accurate method, particularly if the titration curve s slope at the equivalence point is small. 

Another method for finding the end point is to plot the first or second derivative of the titration curve. The slope of a titration curve reaches its maximum value at the inflection point. The first derivative of a titration curve, therefore, shows a separate peak for each end point. The first derivative is approximated as ApH/AV, where ApH is the change in pH between successive additions of titrant. For example, the initial point in the first derivative titration curve for the data in Table 9.5 is... 

Titration curves for a weak acid with 0.100 M NaOH—(a) normal titration curve (b) first derivative titration curve ... 

---