Related Experiment Video
Updated: Jun 28, 2026

09:50
Electrochemically and Bioelectrochemically Induced Ammonium Recovery
Published on: January 22, 2015
Automated square-wave anodic-stripping voltammetry with a flow-through cell and matrix exchange
1Department of Chemistry, University of Iowa, Iowa City, IA, 52242, U.S.A.
Talanta
|March 1, 1982
Summary
A new, highly sensitive instrument for square-wave anodic-stripping voltammetry was developed. This versatile system, controlled by a microcomputer, enables precise analysis of trace metals like Cadmium (Cd) in various sample matrices.
Area of Science:
- Electroanalytical Chemistry
- Analytical Instrumentation
- Trace Metal Analysis
Background:
- Square-wave anodic-stripping voltammetry (SWASV) is a powerful technique for trace metal detection.
- Existing instrumentation may lack versatility in sample matrix handling and parameter control.
- Development of a highly sensitive and adaptable SWASV system is crucial for advanced environmental and chemical analysis.
Purpose of the Study:
- To describe a novel, extremely sensitive, and versatile instrument for square-wave anodic-stripping voltammetry.
- To demonstrate the instrument's capability to change solution matrices between deposition and stripping steps.
- To showcase the microcomputer-controlled system's flexibility in parameter adjustment for optimized trace metal analysis.
Main Methods:
- Development of a microcomputer-controlled instrument for square-wave anodic-stripping voltammetry.
- Incorporation of a flow-through cell allowing matrix changes between deposition and stripping.
- Utilization of a custom-built static mercury drop electrode.
- System control via microcomputer for adjustable square-wave parameters, scan potentials, deposition time, scan rate, sensitivity, and drop size.
Main Results:
- Demonstrated high sensitivity with calibration graphs for Cadmium (Cd) in the ranges 0.2-40 ng/ml and 0.1-1 ng/ml.
- Evaluated the reproducibility of the static mercury drop electrode.
- Successfully applied the method for Cd analysis in a sodium chloride (NaCl) sample, showcasing practical applicability.
Conclusions:
- The developed instrument offers exceptional sensitivity and versatility for SWASV.
- The flow-through cell and microcomputer control facilitate adaptable trace metal analysis.
- The system is a valuable tool for accurate quantification of trace metals in complex matrices.
More Related Videos
Related Concept Videos
Voltammetry: Stripping Methods
Anodic Stripping Voltammetry (ASV), Cathodic Stripping Voltammetry (CSV), and Adsorptive Stripping Voltammetry (AdSV) are electrochemical techniques used to determine trace amounts of analytes in solution. These methods involve applying a potential to an electrode and measuring the resulting current.
Anodic Stripping Voltammetry (ASV)
ASV is used to determine metals and metalloids at trace levels. It involves two steps: deposition and stripping. First, a negative potential is applied to the...
Anodic Stripping Voltammetry (ASV)
ASV is used to determine metals and metalloids at trace levels. It involves two steps: deposition and stripping. First, a negative potential is applied to the...
Voltammetric Techniques: Pulse Voltammetry
Differential-pulse voltammetry (DPV) is a type of voltammetry that involves applying a series of voltage pulses to an electrochemical cell while measuring the resulting current. In DPV, the differential pulse or small potential pulses are superimposed on a linear potential sweep. The magnitude of these pulses is typically small, often in the millivolt range. Each voltage pulse lasts a short duration, usually in the order of a few milliseconds, and is applied at regular intervals along the...
Voltammetric Techniques: Cyclic Voltammetry
Cyclic voltammetry (CV) is an electrochemical technique used to investigate the redox properties of a chemical species. It involves measuring the current response of an electrochemical cell as a function of the applied potential. The setup for cyclic voltammetry typically consists of a working electrode, a reference electrode, and a counter electrode—all immersed in an electrolyte solution. The working electrode is where the redox reaction of interest occurs, while the reference electrode...
Voltammetry: Overview
Voltammetry is an electroanalytical technique in which the current flowing through an electrochemical cell is measured as a function of applied potential, typically under conditions of concentration polarization. The technique provides valuable information about redox-active species, and the current response is plotted as a voltammogram.
A voltammetric cell uses three electrodes: a working electrode, a reference electrode, and an auxiliary electrode. The redox reactions occur in the working...
A voltammetric cell uses three electrodes: a working electrode, a reference electrode, and an auxiliary electrode. The redox reactions occur in the working...
Voltammetric Techniques: Linear-Scan (E vs Time)
Polarography is a classical voltammetric technique used to analyze electrochemical reactions. This method applies a linear potential sweep to a dropping mercury electrode (DME), and the resulting current is measured. A dropping mercury electrode is commonly used as the working electrode in polarography. It consists of a capillary tube filled with mercury, where the tiny droplet forms at the tip. This droplet continuously drops from the capillary, creating a new electrode surface for each...
Controlled-Current Coulometry: Overview
Controlled current coulometry, also known as amperostatic coulometry, is a technique used in electrochemical analysis to measure the quantity of a substance through the controlled passage of current. It involves the application of a constant current to an electrochemical cell containing the analyte of interest. As the current flows through the cell, the analyte undergoes a redox reaction at the electrode surface, resulting in a charge transfer. By monitoring the time required for a certain...

