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types of complexometric titration
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Complexometric titration is defined as a form of volumetric analysis in which the formation of a coloured complex is used to indicate the endpoint of the titration (1). Complexometric titrations rely on the formation of complexes between metal ions and compounds capable of donating electrons to form a stable, soluble complex (2). The complex is formed as a result of metal ions being titrated with a complexing agent or ligand. The principle of complexometric titrations is based on a simple ion being transformed into a complete ion and using a metal indicator to determine the endpoint (3), and the displacement of water from the solvation sphere of the metal ions by ligands (5). Different indicators are used in complexometric titrations as they have different pH ranges as well as detecting different metals in those ranges (1). Therefore complexometric titrations are useful in determining a mixture of different metals (1).
There are 4 types of complexometric titrations, namely direct titration, back titration, replacement titration and indirect titration (3). Direct titration is similar to an acid-base titration, whereby a standard chelon solution is added to the metal ion until the endpoint is detected (3). Although this method is the most convenient, it is limited by slow complexation reaction and interference due to the presence of other ions (3). In back titration an excess of standard EDTA solution is added to the metal solution to be analysed and the excess is back titrated to with a standard solution of a second metal ion (3). In replacement titration, the metal to be analysed displaces quantitatively from the complex (3). When the first 2 methods do not give a sharp endpoint, the metal may be determined by the displacement ...
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...rated against a known volume of EDTA
References
www.srmuniv.ac.in/downloads/Complexometric_Titration.pdf
Cairns, D. (2008). Essentials of Pharmaceutical Chemistry. Third Edition. Pharmaceutical Press. London. Great Britain. p152 – 154
Husain, A. (2007). Pharmaceutical Analysis: Theoretical Basis of Analysis. Complexometric Titrations. Department of Pharmaceutical Chemistry, Faculty of Pharmacy. Jamia Hamdard. Hamdard Nagar New Delhi. India
www.pharma-board.com/fop-drs/drawady/3rd_partII.pdf
Tandlich, R. (2014). Pharmaceutical Chemistry. Complexometric Titrations. Rhodes University. Grahamstown. South Africa. Slide 59-82
www.bionmr.un/edu/courses/chem221/lectures/chapter-12.ppt
Chemlab.truman.edu/CHEM222manual/pdf/edta.pdf
Furia, T. E. (1980). CRC Handbook of Food Additives, Second Edition, Volume 2. CRC Press. Florida. United States of America. p274
1-2 droplets of phenolphthalein indicator were put in. It was titrated until red color can be observed.
Stability of a complex in solution is known to be the separation of two compound resulting in equilibrium state, theoretically it was observed that; there greater association, the higher the stability of the
There are a few changes that should be made to the procedure so that the experiment could generate better results. More time should be allowed to dissolve the tablets as if they are not dissolved colour changes are harder to identify during the titration and also the results are less accurate. The acid used should also be more concentrated as a 0.5mol or 0.3mol would mean a smaller amount of acid would be required.
Note: The revised version of the method (9.1.) differs in one major point from reference 9.4.: Preparation of samples and standards for analysis. It is now ...
Although the majority of the copper remained within the beaker, some of the copper went along with the supernatant liquid that was removed. Since some copper molecules were inadvertently removed from the beaker, the overall weight of the copper later measured less than what it should have been. Another laboratory error was how zinc was not fully extracted from the solution. While taking out the zinc that was used to separate the copper ion from the chlorine ion, some residue could have been left behind. As a direct result of stirring around the solid zinc to knock off the copper, some zinc from the original piece broke off. Not knowing how much zinc was left behind likely caused the weight of the later measured copper to be greater than what it should have been. Overall, the weight variation of the copper sample, after the procedure, was not 100% accurate since it gain weight from zinc and loss some weight due to
The purpose of this lab is to understand the concepts of pH and buffers and how to make a buffer in the laboratory. Also, how to perform the titration process and identify the values of pKa, equivalence point, and the unknown buffer based on the titration process.
Before beginning the experiment observe and record the physical appearance of all the chemicals used in the experiment. First write a balanced chemical equation that has Zinc iodide as product when Barium iodide and zinc sulfate are used. To begin today’s lab, weigh a small test tube on a scale that goes to the hundredths place. Using a clean spatula add .45 g + .03 grams of zinc sulfate heptahydrate (.25 g + .03 grams if zinc sulfate is used) into the small test tube. Dissolve the sample in 2 mL of deionized water. Make sure al of the powder is mixed with the water, stopper the test tube and shake for about 1 to 1 ½ minutes to dissolve. Let the test tube stand and weigh another small test tube. Depending on what is being used, .61 g +.03
By comparing the absorption spectrum of phenol red in basic and acidic solutions, the red (basic) form had a much narrower and higher λ max (560nm) than the yellow form (420nm). As a result, the red form of phenol red was more sensitive with pH changes and it was used in for an assay in part B. In part B, the standard calibration curve was generated in order to determine the concentration of phenol red in the unknown 2B. From the slope, the average concentration of the unknown 2B was 0.001009 M. More importantly, the % difference of unknown trials was low (0.40%), indicating the high precision and reliability of the result. In part C, the pKa of the phenol red can be determined by plotting pH as a function of log ([A-])/([HA]). The pKa and
The Mohr chloride titration method determines the chloride content in a solution in order determine molarity.
Varying the n value carries out the experiment. Absorbencies of each of the ZLn complexes are obtained. The sum of the concentrations of the metal, Z, and the ligand, L, are kept equal. With the ratio of the ligand to the metal in the solution with the maximum absorbance for the ZLn complex, the value of n can be determined as well as the composition of ZLn.
Gusdinar T. COMPLEXOMETRIC TITRATION An application method of Inorganic Pharmaceutical Analysis [homepage on the internet] . No date. [cited 2014 Mar 20]. Available from: http://download.fa.itb.ac.id/filenya/Handout%20Kuliah/Inorganic%20Pharmaceutical%20Analysis%202008/English%20Version/05.%20COMPLEXOMETRIC%20TITRATION.pdf.
Due to the nature of amino acids, a titration curve can be employed to identify
This experiment consists of titrating the ferrous ion with permanganate ion to study the oxidation-reduction reaction. The ions react in acidic solution to give ferric ion and a reduced ionic form of manganese. All the reactants and products except permanganate ion are weakly colored, whereas permanganate is a very intensely colored ion. Then a solution of permanganate is removed as long as there is a ferrous ion present to react with it. But as soon as the entire ferrous ion has been oxidized, the next small portion of added permanganate colors the solution. The first appearance of a permanent pink color indicates the endpoint of the experiment. From the titration it will be able to calculate the percentage of iron in the sample from the data.
Titration is a technological process in which a solution, known as a titrant, is slowly and carefully added from a burrette into a fixed volume of another solution (known as the sample). In an acid-base titration an acid neutralizes a base or vice versa. This process is maintained untill the reaction between the titrant and the sample (acid and the base) is judged to be complete. The reaction is judged to be complete when the endpoint is reached. An endpoint in a titration analysis is referred to as the point at which no more titrant is added due to an observable colour change of an indicator. Indicators can be used to find an endpoint because they change colour when the pH of a solution changes and an endpoint in a titration is an empirical approximation of the equivalence point, which is the point of major pH change in the titration sample due to the fact that equal chemical amounts of reactants have been combined at that point. All indicators have a pH range, which is the range of pH values at which the colour of the indicator changes. Thus
In this experiment three different equations were used and they are the Stoichiometry of Titration Reaction, Converting mL to L, and Calculating the Molarity of NaOH and HCl (Lab Guide pg. 142 and 143).