Electrogravimetry and Coulometry. Potentiometric measurements are made in the absence of current flow. The measured potential is that of a galvanic or voltaic . 22A The effect of current on cell potential When there is a net current in an electrochemical cell, the measured potential across the two electrodes is no longer. PDF | On Mar 3, , Subhrangsu Dey and others published Electrogravimetry and Coulometry.

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Adsorptive stripping voltammetry Amperometric titration Anodic stripping voltammetry Bulk electrolysis Cathodic stripping voltammetry Chronoamperometry Coulometry Cyclic voltammetry Differential pulse voltammetry Electrogravimetry Hydrodynamic technique Linear sweep voltammetry Normal pulse voltammetry Polarography Potentiometry Rotated electrode voltammetry Squarewave voltammetry Staircase voltammetry Voltammetry.

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Bulk Electrolysis: Electrogravimetry and Coulometry – ppt video online download

It is known that in the phenomenon of polarization the products of electrolysis exerts a back EMFwhich reduces the actual EMF of the cell. In other projects Wikimedia Commons. This article about analytical chemistry is a stub. Retrieved from ” https: In this process, the analyte solution is electrolyzed. If you wish to download it, please recommend it to your friends in any social system. OK Other Electrochemical Methods. Share buttons are a little bit lower.


Amperostat Auxiliary electrode Dropping mercury electrode Electrode Electrolytic cell Galvanic cell Hanging mercury drop electrode Ion selective electrode Mercury coulometer pH meter Potentiostat Reference electrode Rotating disk electrode Rotating ring-disk electrode Salt bridge Saturated calomel electrode Silver chloride electrode Standard hydrogen electrode Ultramicroelectrode Voltameter Working electrode.


The cathode is maintained at V versus SCE throughout the electroggavimetry. The proportionality constant between the quantity measured and the analyte mass is calculated from accurately known physical constants. The applied voltage which is just sufficient to overcome the back EMF due to polarization and also to bring about the electrolysis of an electrolyte without any hindrance is known as decomposition potential. Reactants are transported to the surface couloometry an electrode by three mechanisms: Concentration polarization occurs because of the finite rate of mass transfer from the solution to the electrode surface.

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The current a and IR drop b decrease steadily with time. Controlling the potential of the electrode is important to ensure that only the metal being analyzed will be deposited on the electrode. Comparison of Voltammetry to Other Electrochemical Methods 1. This page was last edited on 19 Aprilat About project SlidePlayer Terms of Service.

By using this site, you agree to the Terms of Use and Privacy Policy. Two additional phenomena, IR drop and elctrogravimetry, must be considered. To use this website, you must agree to our Privacy Policyincluding cookie policy. Unsourced material may be challenged and removed. Feedback Privacy Policy Feedback. Download ppt “Bulk Electrolysis: Ag AgCl sCl- 0.


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Electrogravimetry – Wikipedia

In the limiting current region, the electrode is said to be completely polarized since its potential can be changed widely without affecting coulometdy current. From Wikipedia, the free encyclopedia. In order to generate a current of I amperes in this cell, a potential that is IR volts more negative than the thermodynamic cell potential must be applied.

Electrogravimetry and Coulometry Chapter 22 Bulk Electrolysis: Thus electrolysis of an electrolyte is possible only when this back EMF is overcome. Please help improve this article by adding citations to reliable sources. The oxidation number of Zn has. If electrogravimery source of potential is applied, no appreciable current will flow through the system, until some minimum potential is applied after which the current will increase as the applied potential increases.

The charge required to convert the analyte to its reaction product is then determined by recording and integrating the current-versus-time curve during the electrolysis.

The instrumentation for potentiostatic coulometry consists of an electrolysis cell, a potentiostat, and a device for determining the charge consumed by the analyte.