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An overview of an acid-base titration experiment, explaining the concept of titration, standard solutions, indicators, and the equivalence point. It also discusses the importance of standardization and the role of primary and secondary standard solutions. examples of acids and their equivalent weights, as well as the importance of precision and accuracy in the experiment.
Typology: Lab Reports
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Exp 13 Volumetric Analysis: Acid-Base titration
Titration - is the measurement of the volume of a standard solution required to completely react with a measured volume or mass of substance being analyzed (also referred to as analyte)
Standard solution - is a solution containing a known concentration of solute.
Standardization - the concentration of a solution is determined by using it to titrate a carefully measured quantity of a primary standard.
Primary standard - is a highly purified compound that serves as a reference material in all volumetric and mass titrimetric methods. (high purity, stable toward air/dried, absence of hydrated waters, cost, soluble in solvent, large molar mass)
Secondary standard solution - titrant that is standardized against a standard solution.
Indicators - are added to analyte solution in order to give an observable physical change (end point) at or near the equivalence point. Typically appearance or disappearance of color, change in color, ppt formed, etc.
Equivalence point - is reached when the amount of added titrant is chemically equivalent to the amount of analyte in sample.
End point - physical change that can be observed associated with the conditions of equivalence.
Titration error - difference in volume or mass between the equivalence point and the end point.
CV = CV dilution only
NaVa = NbVb normality
Normality = number of eq wt solute L solution
Eq wt of acid - is defined as mass of acid that will furnish 1 mol H+^ or that will react with 1 mol OH-.
examples
HCl H+^ + Cl-^ 1eq/mol HCl H 2 SO 4 2H+^ + SO 4 2-^ 2eq/mol H 2 SO 4 NaOH Na+^ + OH-^ 1eq/mol NaOH Ca(OH) 2 Ca2+^ + 2OH-^ 2eq/mol Ca(OH) 2
Avg N ± s N minimum 3 runs ± 0.005 N (around ± 0.5 mL) for the std and 3 for the unknown.
Note: s must match avg N decimal place
Acid quantities 10 mL per run not 20 mL as in manual.
Take 150 mL 0.1 N NaOH 45 mL 0.1000 N H 2 SO 4 standard solution 45 mL unknown assigned by TA
Example 2: Enthalpy experiment
Discussion When reactions occur, there is an accompanying change in energy. Typically this energy change is in the form of heat (enthalpy). A reaction usually either absorbs heat (endothermic) or releases heat (exothermic) to the surroundings. The enthalpy of the reaction between HCl and NaOH was investigated. It was found that -58.3 kJ/mol of heat was involved in this reaction. This means that when HCl and NaOH are reacted, 58.3 kJ/mol of heat is released to the surroundings indicating that this reaction is exothermic. The surroundings in this experiment included the salt solution produced in the reaction and the coffee cup calorimeter.
This experiment was conducted three times with good precision (standard deviation of 0.1 kJ/mol) and accuracy of approximately 5% from the theoretical enthalpy of HCl (-55.4 kJ/mol).
There are two main sources of error that could interfere with the accuracy and precision of this experiment. First, the calorimeter used in this experiment was a Styrofoam cup with cardboard being placed on top of the cup as the lid. Heat could escape through the unsealed lid during the experiment causing inaccurate temperature readings during the experiment. Second, the two thermometers used in the experiment were not calibrated: one each in the HCl and NaOH solutions before they were mixed. The two thermometers indicated different room temperature readings. When the two solutions were mixed, the same thermometer that was in the HCl solution was used in the mixture making the measured change in temperature for the NaOH solution questionable. However, reasonable results were still obtained despite using a calorimeter that was non-technical (coffee cup with cardboard).