Want this question answered?
it give sharp end point for coloured soln. even for those that are precipitate out in other volumetric titration
types of conductometric titration: acid base titration complexometric titration replacement titration redox titration precipitation titration
In the determination of iron in pharmaceutical preparations In the determination of iron in pharmaceutical preparations
Direct titration, Indirect titration, back titration, replacement titration and so on
over titration is when too much titrant is added to the analyte in a titration procedure.
it give sharp end point for coloured soln. even for those that are precipitate out in other volumetric titration
command
command
types of conductometric titration: acid base titration complexometric titration replacement titration redox titration precipitation titration
In the determination of iron in pharmaceutical preparations In the determination of iron in pharmaceutical preparations
Direct titration, Indirect titration, back titration, replacement titration and so on
A unstructured application is hard to maintain, difficult to debug, and generally performs slower than a properly structured and organized application.
over titration is when too much titrant is added to the analyte in a titration procedure.
Titration is a method of chemical analysis; for example: - volumetry - potentiometric titration - amperometric titration - radiometric titration - Karl Fisher titration - spectrophotometric titaration - viscosimetric titration and other methods
A program or an application or a utility are computer software that perform tasks
There are various types of titration. It is dependent on the conditions used and the reactants and desired products. Some of them are acid-base titration, redox titration, colorimetric titration and thermometric titration.
Radiometric titration is "regular" titration, but with the incorporation of a radioactive indicator to monitor the end-point. And that's right from the IUPAC Compendium of Chemical Terminology. If you need an example, use the link provided to a post on the radiometric titration of hexachloro-platinate (IV). It's a bit esoteric, but it will serve to exemplify the idea behind radiometric titration. It's pretty clear that when working with two precipitates (co-precipitation), the analyst would need a way to differentiate them. In the case cited, the application of radioactive cæsium-137 will permit the observer to more quickly and easily find a cutoff point at which to terminate the titration.