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Why is a high supporting electrolyte concentration used in most electroanalytical procedures?

Short Answer

Expert verified

To reduce the effect of moving electroactive spaces caused by electrostatic attraction, So we use high supporting electrolyte.

Step by step solution

01

Electroanalytical procedures.

Electroanalytical procedures make use of electrodes, which are electrically conductive probes that make contact with the analyte solution.

The electrodes are accustomed to measure an electrical parameter of the answer in conjunction with electric or electronic devices to which they're coupled.

02

Reason for using high supporting electrolyte.

A high supporting electrolyte concentration is employed to scale back the cell resistance, which lowers the IRdrop, and to reduce the impacts of electrostatic attraction on migration to the electrode surface.

03

Reason for top supporting electrolyte concentration employed in most electroanalytical procedures.

In most electroanalytic techniques, a high supporting analyte is used to limit the effect of moving electroactive species induced by electrostatic attraction so as to manage ionic strength, electrode potential, and conductivity, among other things.

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Most popular questions from this chapter

What is the purpose of the electrodeposition step in stripping analysis?

A new method for determining ultrasmall (nL) volumes by anodic stripping voltammetry has been proposed (W. R. Vandaveer and I. Fritsch, Anal. Chem.2002,74,3575,DOI:10.1021/ac011036s). In this method, a metal is exhaustively deposited from the small volume to be measured onto an electrode, from which it is later stripped. The solution volume Vsis related to the total charge Qrequired to strip the metal by

Vs=QnFC

where nis the number of moles of electrons per mole of analyte, Fis the faraday, and Cis the molar concentration of the metal ion before electrolysis.

(a) Beginning with Faradayโ€™s law (see Equation 22-8), derive the above equation for Vs.

(b) In one experiment, the metal deposited was Ag(s)from a solution that was 8.00mMin AgNO3. The solution was electrolyzed for 30min at a potential of -0.700Vversus a gold top layer as a pseudo reference. A tubular nano band electrode was used. The silver was then anodically stripped off the electrode using a linear-sweep rate of 0.10V/s. The following table represents idealized anodic stripping results. By integration, determine the total charge required to strip the silver from the tubular electrode. You can do a manual Simpsonโ€™s rule integration or do the integration with Excel From the charge, determine the volume of the solution from which the silver was deposited.

(c) Suggest experiments to show whether all the Ag+was reduced to Ag(s)in the deposition step.

(d) Would it matter if the droplet were not a hemisphere? Why or why not?

(e) Describe an alternative method against which you might test the proposed method.

Why is a high supporting electrolyte concentration used in most electroanalytical procedures?

A solution containing cd2+was analyzed voltammetrically using the standard addition method. Twenty-five milliliters of the deaerated solution, which was 1Min HNO3, produced a net limiting current of 1.41ฮผ{A} at a rotating mercury film working electrode at a potential of -0.8V(versus SCE). Following addition of 5.00MLof a 2.50ร—10-3Mstandard Cd2+solution, the resulting solution produced a current of 4.93ฮผ{A}. Calculate the concentration of Cd2+the sample.

What is the purpose of the electrodeposition step in stripping analysis?

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