Anodic stripping voltammetry and MIPS (disambiguation): Difference between pages
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[[Image:Linear Potential Sweep Anodic Stripping Voltammetry.JPG|right|400px|thumb|'''A:''' Cleaning step, '''B:''' Electroplating step, '''C:''' Equilibration step, '''D:''' Stripping step]] |
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'''Anodic stripping voltammetry''' is a voltammetric method for quantitative determination of specific ionic species. The [[analyte]] of interest is [[electroplating|electroplated]] on the [[working electrode]] during a deposition step, and [[oxidized]] from the electrode during the stripping step. The current is measured during the stripping step. The oxidation of species is registered as a peak in the current signal at the potential at which the species begins to be oxidized. The stripping step can be either [[Linear sweep voltammetry| linear]], [[Staircase voltammetry| staircase]], [[Squarewave voltammetry| squarewave]], or pulse. |
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==Electrochemical Cell Set-Up== |
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Anodic stripping voltammetry usually incorporates three electrodes, a [[working electrode]], [[auxiliary electrode]] (sometimes called the counter electrode), and [[reference electrode]]. The [[solution]] being analyzed usually has an [[electrolyte]] added to it. For most standard tests, the working electrode is a [[mercury (element)|mercury]] film electrode. The mercury film forms an [[amalgam]] with the analyte of interest, which upon oxidation results in a sharp peak, improving resolution between analytes. The mercury film is formed over a [[glassy carbon]] electrode. A mercury drop electrode has also been used for much the same reasons. In cases were the analyte of interest has an oxidizing potential above that of mercury, or where a mercury electrode would be otherwise unsuitable, a solid, inert metal such as [[silver]], [[gold]], or [[platinum]] may also be used. |
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==Steps== |
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Anodic stripping voltammetry usually incorporates 4 steps if the working electrode is a mercury film or mercury drop electrode and the solution incorporates stirring. The solution is stirred during the first two steps at a repeatable rate. The first step is a cleaning step; in the cleaning step, the potential is held at a more oxidizing potential than the analyte of interest for a period of time in order to fully remove it from the electrode. In the second step, the potential is held at a lower potential, low enough to reduce the analyte and deposit it on the electrode. After the second step, the stirring is stopped, and the electrode is kept at the lower potential. The purpose of this third step is to allow the deposited material to distribute more evenly in the mercury. If a solid inert electrode is used, this step is unnecessary. The last step involves raising the working electrode to a higher potential (anodic), and stripping (oxidizing), the analyte. As the analyte is oxidized, it gives off electrons which are measured as a current. |
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==Sensitivity== |
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Anodic stripping voltammetry can detect μg/l concentrations of analyte. |
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==See also== |
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* [[Cathodic stripping voltammetry]] |
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* [[Adsorptive stripping voltammetry]] |
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* [[Voltammetry]] |
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* [[Electroanalytical Methods]] |
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* [[Electroplating]] |
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* [[Amalgam]] |
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==References== |
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# http://www.drhuang.com/science/chemistry/electrochemistry/polar.doc.htm |
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# http://www.chemistry.msu.edu/courses/cem837/Anodic%20Stripping%20Voltammetry.pdf |
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# http://ocw.kfupm.edu.sa/user/CHEM54201/Anodic%20stripping%20good.pdf |
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# Wang, J. (1985). Stripping Analysis: Principles, Instrumentation, and Applications, VCH Publishers, Inc., Deerfield Beach, Florida. |
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# http://www.amelchem.com/download/items/voltammetry/manuals/eng/manual_eng.pdf |
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[[Category:Analytical chemistry]] |
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{{analytical-chemistry-stub}} |
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{{electroanalytical}} |
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Revision as of 01:49, 10 October 2008
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