Practical Analytical Chemistry (1)

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Practical Analytical Chemistry (1) Faculty of Pharmacy Practical Analytical Chemistry (1) Department of Pharmaceutical Chemistry Practical (7)

pH: Measurement and Uses Theory One of the most important properties of an aqueous solution is hydrogen ion concentration. The concentration of H+1 (or H3O+1) affects the solubility of inorganic and organic species, the nature of complex metal cations, the path taken and the rates of many chemical reactions. For conciseness and convenience, the concentration of H+1 is frequently expressed as the pH of the solution rather than hydrogen ion molarity. pH is defined by the equation: PH = -log [H+1] (Eq. 1) Where the logarithm is taken to the base 10. If [H+1] is 1 x 10-4 moles per liter, the pH of the solution is 4. If [H+1] = 5 x 10-2 M, pH = 1.3.

Basic solutions are also described in terms of pH Basic solutions are also described in terms of pH. In water the following relation exists: [H+1] x [OH-1] = Kw = 1.00 x 10-14 at 25 ºC (Eq. 2) Since [H+1] equals [OH-1] in pure water, by Equation 2, [H+1] must be 1 x 10-7 M. Therefore, the pH of absolutely pure water is 7. Solutions in which [H+1] > [OH-1] are acidic and will have a pH < 7. When [H+1] < [OH-1], a solution is basic and pH >7. A solution with a pH of 10 will have [H+1] = 1 x 10-10 M and [OH-1] = 1 x 10-4 M. PH Measurement: The pH of a solution can be determined experimentally in several ways. One is to use an indicator, a soluble dye whose color is sensitive to pH. Indicator colors change over a relatively short (about 2-unit) pH range. When properly chosen, they give the approximate pH of solutions. Two common indicators are litmus, usually used on paper, and phenolphthalein, commonly used in solution in acid-base titrations.

Litmus changes from red to blue in the pH range 6 to 8 Litmus changes from red to blue in the pH range 6 to 8. Phenolphthalein changes from colorless to pink in the range 8 to 10. Any one indicator is useful for determining pH only in the region where it changes color. Indicators are available for measuring pH in any part of the scale. Universal indicator papers, which contain a mixture of several indicators and change color over a wide pH range, are also in common use. An electronic pH meter is used for more precise measurements. A pH meter determines pH from the electrical potential between two electrodes in a solution. The potential varies with pH and activates an analog or digital meter calibrated to read pH directly to the nearest 0.01 or 0.001 units. A pH meter is used when reliable knowledge or control of pH is necessary.

Buffers Solutions which undergo only a small change in pH when small quantities of acid or base are added to them are called buffers. For example, human blood is a complex buffered mixture with a normal pH range of 7.35 - 7.45. Three different buffer systems keep blood pH from varying more than ± 0.1 units. A buffer solution is prepared from approximately equal amounts of a weak acid and its salt with a strong base or from a weak base and its salt with a strong acid. The dependence of [H+1] on the ratio of the concentration of undissociated acid to the acid anion is seen in equation 14: HA(aq) 􀂕 H+1 (aq) + A-1(aq) (Eq. 12) Ka = [H+1][A-1]/[HA] (Eq. 13) [H+1] = Ka [HA]/ [A-1] (Eq. 14) Taking the log of both sides and rearranging the equation gives the Henderson-Hasselbalch equation that relates the pH of a buffer solution to the pKa of the acid and the anion/acid concentration ratio. pH = pKa + log([A-1]/[HA]) (Eq. 15) If a small quantity of strong base is added to a buffer solution, the added OH-1 reacts with the buffer HA to form water and A-1 both of which are already present in large amounts. [H+1] decreases only slightly, since the strong base hydroxide is replaced by the weak base [A-1]. If a small quantity of strong acid is added to a buffer, H+1 reacts with the buffer A-1 to produce the weak acid HA which is already present. In either case, the [HA]/[A-1] ratio, which controls pH, changes little and the pH remains almost unchanged. Solutions of weak bases and their salts also contain an acid/base conjugate pair and behave in a similar manner to stabilize pH

Procedure: Your instructor will show you how to calibrate the pH meter and read it to 0.01 pH unit. Take care not to damage the delicate glass hydrogen ion electrode by rubbing it against another glass surface. It’s best to use a plastic beaker. For highest accuracy, the meter must be calibrated with a buffer solution of known pH close to the range where you will be making your measurements. 1. Measurement of pH of Salt Solutions Put about 25 mL of each of the following solutions in a plastic beaker and measure its pH: 0.1M NaCl, 0.1 M Na2CO3, 0.1 M NH4NO3and 0.1 M NaHCO3.

2. The pH of a Buffer Solution Prepare a buffer solution by adding 4.10 g of Lead acetate to 8.5 mL of 6.0 M acetic acid. Dilute the solution to 100 mL with distilled water and mix. (As an exercise before you come to lab, verify that this solution contains equal concentrations of acetic acid and acetate ion.) Label four small plastic beakers 1 through 4. Put 40 mL of this buffer solution into each of beakers 1 and 2. Put 40 mL of distilled water into each of beakers 3 and 4. Measure the pH of each solution. Pipet 1.0 mL of 6.0 M HC1 into beakers 1 and 3. Pipet 1.0 mL of 6.0 M NaOH solution into beakers 2 and 4. Stir each solution and measure its pH again.  

1: pH of Salt Solutions Solution Measure PH 0.1M NaCl 0.1M Na2CO3 Points for discussion 1: pH of Salt Solutions Solution Measure PH 0.1M NaCl 0.1M Na2CO3 0.1M NH4NO3 0.1M NaHCO3

2: pH of Buffer Solutions Measure PH Beaker 1, Buffer Beaker 2, Buffer Beaker 3, Distilled Water Beaker 4, Distilled Water Beaker 1, Buffer + HCl Beaker 2, Buffer + NaOH Beaker 3, Distilled Water + HCl Beaker 4, Distilled Water + NaOH