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What is the theoretical background of potentiometry? - Metrohm

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1.4.2. The Metrosensor «Long Life» referencesystemMost electrodes are equipped with <strong>the</strong> silver/silverchloride reference system. The solubility product <strong>of</strong>silver chloride in water <strong>is</strong> very small (10 -10 mol/L). In<strong>the</strong> concentrated, chloride-containing solution <strong>of</strong> <strong>the</strong>reference electrolyte soluble complexes <strong>of</strong> <strong>the</strong> series(AgCl 2 ) - , (AgCl 3 ) 2- , (AgCl 4 ) 3- are formed. Th<strong>is</strong> meansthat <strong>the</strong> reference system poses several problems.Outside <strong>the</strong> electrode <strong>the</strong> chloride concentration <strong>is</strong>frequently lower and <strong>the</strong> complexed silver chlorideprecipitates in <strong>the</strong> region surrounding <strong>the</strong> diaphragm(«liquid junction»). The result: precipitated silver chlorideblocks <strong>the</strong> diaphragm, <strong>the</strong> response time <strong>of</strong> <strong>the</strong>pH electrode increases and with time <strong>the</strong> electrodebecomes inactive. A fur<strong>the</strong>r problem <strong>is</strong> presented by<strong>the</strong> dependency <strong>of</strong> <strong>the</strong> solubility product <strong>of</strong> AgCl on<strong>the</strong> temperature. If <strong>the</strong> electrode <strong>is</strong> used at a differenttemperature <strong>the</strong>n <strong>the</strong> equilibrium that determines <strong>the</strong>potential <strong>of</strong> <strong>the</strong> reference electrode must be reestabl<strong>is</strong>hed.The larger <strong>the</strong> surface with solid AgCl in relationshipto <strong>the</strong> electrolyte volume, <strong>the</strong> shorter <strong>the</strong>time required. The «Long Life» reference system preventshigh concentrations <strong>of</strong> complexed AgCl fromoccurring in <strong>the</strong> outer electrolyte, as <strong>the</strong> silver chloridereservoir <strong>is</strong> connected with <strong>the</strong> outer electrolyteby a highly effective diffusion barrier. The concentration<strong>of</strong> <strong>the</strong> silver complex in <strong>the</strong> reference electrolyteremains low. Even after one year <strong>the</strong> concentration<strong>of</strong> silver chloride in <strong>the</strong> outer electrolyte has onlyreached 5% <strong>of</strong> <strong>the</strong> saturation value.Figure 9:Conventional Ag/AgCl/KClsystem. The chloride concentrationoutside <strong>the</strong> electrode<strong>is</strong> usually lower than in <strong>the</strong>electrolyte chamber. Thesoluble silver chloride complexesprecipitate out in<strong>the</strong> region surrounding <strong>the</strong>diaphragm and may block it.Figure 10:The <strong>Metrohm</strong> «Long Life»reference system. Thed<strong>is</strong>solved AgCl <strong>is</strong> retainedin <strong>the</strong> AgCl cartridge andcan no longer block <strong>the</strong>diaphragm.The advantages <strong>of</strong> <strong>the</strong> «Long Life» referencesystems at a glance:• Long working life <strong>of</strong> <strong>the</strong> electrode• Rapid response to changes in pH• Rapid response to temperature changes• Greatly reduced reaction between Ag + and samplesolution, e.g. if th<strong>is</strong> latter contains sulfide ionsBlocking <strong>the</strong> diaphragm by crystallized AgCl alsoaffects <strong>the</strong> electrolyte flow. If <strong>the</strong> «Long Life» referencesystem <strong>is</strong> used <strong>the</strong>n <strong>the</strong> flow <strong>of</strong> <strong>the</strong> KCl solutionthrough <strong>the</strong> diaphragm into deionized water onlydecreases slightly. In a conventional electrode <strong>the</strong>flow <strong>is</strong> reduced by more than 90% in only 10 days.As in <strong>the</strong> «Long Life» reference system <strong>the</strong> silver chloride<strong>is</strong> present in a smaller volume <strong>of</strong> potassium chloridesolution, <strong>the</strong> <strong>the</strong>rmodynamic equilibrium betweensilver, silver chloride (solid) and silver chloride(d<strong>is</strong>solved) <strong>is</strong> establ<strong>is</strong>hed very quickly and <strong>the</strong> potential<strong>of</strong> <strong>the</strong> reference electrode becomes stable after avery short time.1.4.3. DiaphragmsFaulty measurements, unstable measured values andvery long response times usually have <strong>the</strong>ir source in<strong>the</strong> «liquid junction» between <strong>the</strong> sample solutionand <strong>the</strong> reference electrode. The diffusion, streamingand Donnan potentials that occur <strong>the</strong>re – which arenormally known toge<strong>the</strong>r as <strong>the</strong> diaphragm potential– have various causes and can result in a very incorrectmeasured value. The measuring error mayassume vast proportions if measurements are madeunder <strong>the</strong> following conditions:• with a blocked, virtually impermeable diaphragm,• in ion-deficient solutions with an unsuitablediaphragm,• in strong acids and bases with an unsuitablediaphragm,• in colloidal solutions.In all such cases errors may occur that cannot betolerated. Th<strong>is</strong> <strong>is</strong> why <strong>the</strong> following questions must bein <strong>the</strong> foreground whenever an electrode and <strong>the</strong>refore<strong>the</strong> optimal type <strong>of</strong> diaphragm are to be selected:• Does <strong>the</strong> reference electrolyte react with <strong>the</strong>sample solution to form a precipitate in <strong>the</strong>diaphragm?• Does <strong>the</strong> electrolyte flow alter <strong>the</strong> composition<strong>of</strong> <strong>the</strong> sample solution in an unacceptable way?• Is <strong>the</strong>re a r<strong>is</strong>k <strong>of</strong> depositing sample solutioncomponents on <strong>the</strong> diaphragm?• Is <strong>the</strong> chemical res<strong>is</strong>tance assured?85

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