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In analytical chemistry, argentometry is a type of titration involving the silver(I) ion. Typically, it is used to determine the amount of chloride present in a sample. The sample solution is titrated against a solution of silver nitrate of known concentration. Chloride ions react with silver(I) ions to give the insoluble silver chloride:
A back titration is useful if the endpoint of the reverse titration is easier to identify than the endpoint of the normal titration, as with precipitation reactions. Back titrations are also useful if the reaction between the analyte and the titrant is very slow, or when the analyte is in a non-soluble solid. [44]
2 I − → I 2 + 2 e − B·I 2 + B·SO 2 + B + H 2 O → 2 BH + I − + BSO 3 BSO 3 + ROH → BHRSO 4. The end point is detected most commonly by a bipotentiometric titration method. A second pair of Pt electrodes is immersed in the anode solution. The detector circuit maintains a constant current between the two detector electrodes during ...
Thus, one standard solution is needed (e.g. HCl) in the direct titration, while two are needed (e.g. HCl and NaOH) in the back-titration. One of the suitable indicators for these titration reactions is Tashiro's indicator. [3] In practice, this analysis is largely automated; specific catalysts accelerate the decomposition. Originally, the ...
Some examples of primary standards for titration of solutions, based on their high purity, are provided: [4] Arsenic trioxide for making sodium arsenite solution for standardisation of sodium periodate solution (until Ph. Eur. 3, Appendix 2001 also for iodine and cerium(IV) sulfate solutions, since Ph. Eur. 4, 2002 standardised by sodium ...
Note that iodometry involves indirect titration of iodine liberated by reaction with the analyte, whereas iodimetry involves direct titration using iodine as the titrant. Redox titration using sodium thiosulphate, Na 2 S 2 O 3 (usually) as a reducing agent is known as iodometric titration since it is used specifically to titrate iodine. The ...
Fig. 15. Titration plot of back-titration of excess EDTA with Cu(II) in NH 3 /NH 4 Cl buffered solution. Direct EDTA titrations with metal ions are possible when reaction kinetics are fast, for example zinc, copper, calcium and magnesium. However, with slower reaction kinetics such as those exhibited by cobalt and nickel, back-titrations are used.
For a strong acid-strong base titration monitored by pH, we have at any i'th point in the titration = [+] [] where K w is the water autoprotolysis constant.. If titrating an acid of initial volume and concentration [+] with base of concentration [], then at any i'th point in the titration with titrant volume ,