1 Metode Titrimetri

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  • KIMIA ANALITIK DASAR 2

  • SILABUSMetode titrimetri; titrasi netralisasi; analisis volumetri untuk reaksi pembentukan endapan dan senyawa kompleks (argentometri); titrasi pembentukan senyawa kompleks; analisis volumetri secara oksidasi-reduksi (redoksimetri); Analisis gravimetri

  • BUKU REFERENSI David Harvey, Modern Analytical Chemistry, Mc Graw-Hill Skoog, D. A. and West, D.M., Fundamentals of Analytical Chemsitry, Holt-Saunders International edition. Vogels Textbook of Quantitative Chemical Analysis, Longman and Scientific, EssexChristian, G.D., Analytical Chemsitry, 5th edition, John Wiley and Sons, Inc., New York.

  • INTRODUCTION TO TITRIMETRY

  • Most common types of titrations : neutralization titrations oxidation-reduction titrations complex formation titration precipitation reactionsIn a titration, increments of titrant are added to the analyte until their reaction is complete. From the quantity of titrant required, the quantity of analyte that was present can be calculated.

  • Figure 1 Titration Setup

  • TITRATIONS IN PRACTICEAccurately add of specific volume of sample solution to a conical flask using a pipetteKnown: volume of sampleUnknown: concentration of analyte in sample

  • Pro Pipet

  • Slowly add standard solution from a burette to the sample solutionKnown: concentration of the titrant

  • Add until just enough titrant is added to react with all the analyteThe end point is signalled by some physical change or detected by an instrumentKnown: volume of the titrantNote the volume of titrant used

  • If we have:HA + BOH BA + H2OThen from the balanced equation we know:1 mol HA reacts with 1 mol BOHanalytetitrantWe also know:CBOH, VBOH and VHA and

  • STANDARD SOLUTIONSStandard solution:Reagent of known concentrationPrimary standard:highly purified compound that serves as a reference material in a titration.Determine concentration by dissolving an accurately weighed amount in a suitable solvent of known volume.

  • primary standard1. High purity100.0%2. Stability toward air3. Absence of hydrate water4. Available at moderate cost5. Soluble6. Large F.W.

  • Secondary standard:compound that does not have a high purityDetermine concentration by standardisation.Titrate standard using another standard.Standard solutions should: Be stable React rapidly with the analyte React completely with the analyte React selectively with the analyte

  • EQUIVALENCE POINTThe amount of added titrant is the exact amount necessary for stoichiometric reaction with the analyte in the sample.An estimate of the equivalence point that is observed by some physical change associated with conditions of the equivalence point.Aim to get the difference between the equivalence point and the end point as small as possible.Titration error:Et = Veq VepEstimated with a blank titrationEND POINTVS

  • Indicators used to observe the end point (at/near the equivalence point)Thymol blue indicator

  • Instruments can also be used to detect end points.Respond to certain properties of the solution that change in a characteristic way.E.g.: voltmeters, ammeters, ohmmeters, colorimeters, temperature recorders, refractometers etc.

  • Add excess titrant and then determine the excess amount by back titration with a second titrant.BACK TITRATIONUsed when: end point of back titration is clearer than end point of direct titration an excess of the first titrant is required to complete reaction with the analyte

  • If we have:HA + BOH BA + H2OThen from the balanced equation we know:1 mol HA reacts with 1 mol BOHanalytetitrantIf I add excess titrant and then react the excess with a second titrant as follows:HX + BOH BX + H2Otitrant 2excessThen from the balanced equation we know:1 mol HX reacts with 1 mol BOH

  • We also know:CBOH, CHX and VHX andWe also know vBOH(total) vBOH(reacted) = vBOH(total) vBOH(excess)

  • From our initial titration:HA + BOH BA + H2O analyte titrantwe then know:CBOH, VBOH(reacted) and VHA and we want to find CHA!

  • In summary:HA + BOH BA + H2Oanalytetitrant reactedVHACBOHHX + BOH BX + H2Otitrant 2titrant excessVHXCHXCBOH vBOH(reacted) = vBOH(total) vBOH(excess)CHA?

  • Example:50.00 ml of HCl was titrated with 0.02 M Ba(OH)2. The end point was reached (using bromocresol green as indicator after 20 ml Ba(OH)2 was added.What is the concentration of the HCl?

  • Example:A 0.8 g sample of iron ore is dissolve in acid. The iron is reduced to Fe2+ and titrated with 0.02 M KMnO4. 40 ml of titrant was added to reach the end point. Calculate the % Fe in the sample.MnO4- + 5Fe2+ + 8H+ Mn2+ + 5Fe3+ + 4H2O

  • MnO4- + 5Fe2+ ..

  • Example:The CO in a 20 L sample of gas was converted to CO2 by passing the gas over iodine pentoxide heated to 150oC:I2O5(s) + 5CO(g) 5CO2(g) + I2(g)The iodine distilled at this temperature was collected in an absorber containing 8 mL of 0.01 M Na2S2O3: I2(aq) + 2S2O32-(aq) 2I-(aq) + S4O62-(aq)The excess Na2S2O3 was back titrated with 2 mL of 0.001 M I2 solution. Calculate the mg CO per liter of sample.

  • I2O5(s) + 5CO(g) 5CO2(g) + I2(g)I2(aq) + 2S2O32-(aq) 2I-(aq) + S4O62-(aq)I2(aq) + 2S2O32-(aq) 2I-(aq) + S4O62-(aq)nreacted =ADDEDEXCESSREACTED

  • I2(aq) + 2S2O32-(aq) 2I-(aq) + S4O62-(aq)I2O5(s) + 5CO(g) 5CO2(g) + I2(g)

  • Calculate the mg CO per liter of sample.