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Types of complexometric titration
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Recommended: Types of complexometric titration
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
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Pharmaceutical journal: A weekly record of pharmacy and allied sciences. Third series, volume XXIV. Bloomsbury Square W.C.: 1894. 26 November 2011. http://books.google.com/books?
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Ostrove, N. M. (2004). Statement of Nancy M. Ostrove, Ph.D., Deputy Director, Division of Drug.
Pauly, S. (2011, February). News from ABC: changes and challenges. Analytical & Bioanalytical Chemistry. pp. 1003-1004. doi:10.1007/s00216-010-4459-0.
As we discussed above that pharmacokinetic and pharmacodynamics can be seen as two sides of the same coin in order to gain better understanding of their efficacy and safety profiles.” Generally it is possible to make fairly robust predictions of the pharmacokinetic profile in man using in vitro systems and preclinical pharmacokinetic studies. A previously published survey on the causes of failure in drug development indicated that inappropriate pharmacokinetics were a major cause such as; factors as low bioavailability due to high extraction or poor absorption characteristics, short elimination half-life leading to short duration of action and excessive variability due to genetic or environmental factors. This observation has led to an increased emphasis on pharmacokinetic input to the drug discovery process throughout the pharmaceutical industry. However, it is important to realise that this may only permit the rejection of compounds to b...
Chemistry: Acid-Base Titration. Purpose: The objective of this experiment were: a) to review the concept of simple acid-base reactions; b) to review the stoichiometric calculations involved in chemical reactions; c) to review the basic lab procedure of titration and introduce the student to the concept of a primary standard and the process of standardization; d) to review the calculations involving chemical solutions; e) to help the student improve his/her lab technique Theory: Titration was used to study acid-base neutralization reaction quantitatively. In acid-base titration experiment, a solution of accurately KHP concentration was added gradually to another solution of NaOH concentration until the chemical reaction between the two solutions was completed. The equivalence point was the point at which the acid was completely reacted with or neutralized by the base.
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.
Analysis of Aspirin Tablets Aim --- To discover the percentage of acetylsalicylic acid in a sample of aspirin tablets. ----------------------------------------------------------------- In order to do this, the amount of moles that react with the sodium hydroxide must be known. This is achieved by using the method of back titration.
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
We consume more of them everyday, but many people do not know what additives do to food and the people that eat it. The average person is amazed by the number of additives injected into our food. Through years of scientific research, it is now possible to comprehend the most commonly used and controversial additives.
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).
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.