Question 1

What are the two main steps in anodic stripping voltammetry?

Accepted Answer

Anodic stripping voltammetry involves deposition and stripping. First, a constant cathodic potential reduces analyte ions to metals deposited on the electrode surface. Next, an anodic potential oxidizes the deposited metals back to ionic states, stripping them off while measuring the resulting current, which is proportional to analyte concentration.

Question 2

How does cathodic stripping voltammetry differ from anodic stripping voltammetry?

Accepted Answer

Cathodic stripping voltammetry uses a mercury electrode that oxidizes and combines with the analyte, forming an insoluble film. The potential then scans toward negative values, reducing and stripping the analyte back into solution while measuring cathodic current. This differs from anodic stripping, which oxidizes deposited metals using positive potential scanning.

Question 3

What is the key advantage of adsorptive stripping voltammetry?

Accepted Answer

Adsorptive stripping voltammetry eliminates the electrolysis step by adsorbing analyte species directly onto the electrode surface without chemical transformation. After adsorption, the analyte is stripped by changing the applied potential, and the resulting current is measured. This technique works for both organic and inorganic species, including pollutants and heavy metals.

Question 4

Why is electrode surface preparation critical in stripping voltammetry?

Accepted Answer

A clean, well-polished electrode surface ensures consistent and reproducible results in stripping voltammetry. Surface contamination or fouling can interfere with analyte deposition and stripping, leading to inaccurate measurements. Proper electrode maintenance is essential for reliable trace-level analysis and minimizing interference from other ions.

Question 5

What role does deposition time play in anodic stripping voltammetry measurements?

Accepted Answer

Deposition time directly affects the amount of analyte reduced and deposited on the electrode surface. Controlling deposition time allows adjustment of the analyte concentration range that can be measured. Longer deposition times accumulate more analyte, improving sensitivity for trace-level detection but requiring careful optimization to avoid electrode saturation.

Question 6

What challenges arise from using mercury electrodes in cathodic stripping voltammetry?

Accepted Answer

Mercury electrodes present toxicity hazards requiring careful handling and disposal protocols. Additionally, reproducible film formation on the mercury surface is difficult to achieve consistently, affecting measurement reliability. These challenges necessitate strict safety procedures and precise experimental control to ensure both operator safety and analytical accuracy.

Question 7

How does solution pH affect stripping voltammetry analysis?

Accepted Answer

Maintaining stable pH is essential for consistent stripping voltammetry results, as pH influences analyte speciation, electrode potential, and deposition efficiency. Fluctuations in pH can alter the reduction potentials of analyte ions and affect their interaction with the electrode surface, compromising measurement accuracy and reproducibility.

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