Category:OSW065e6243e2a658358ce9267455204750: Difference between revisions

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      ],
      "uuid": "065e6243-e2a6-5835-8ce9-267455204750",
-     "iri": "chameo:PotentiometricStrippingAnalysis",
+     "iri": "https://w3id.org/emmo/domain/characterisation-methodology/chameo#PotentiometricStrippingAnalysis",
      "name": "PotentiometricStrippingAnalysis",
      "label": [
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      ],
      "meta": {
-         "uuid": "b5db4a2a-8b29-4e0e-b550-582fbb93ad64",
+         "uuid": "bf6b9d12-ca7c-4cc0-9050-9704615d6d6b",
          "wiki_page": {
              "title": "OSW065e6243e2a658358ce9267455204750",

Latest revision as of 06:05, 1 March 2025

PotentiometricStrippingAnalysis
ID	OSW065e6243e2a658358ce9267455204750
UUID	065e6243-e2a6-5835-8ce9-267455204750
Label	PotentiometricStrippingAnalysis
Machine compatible name	PotentiometricStrippingAnalysis
Statements (outgoing)

Statements (incoming)

Description

Two-step electrochemical measurement in which 1) material is accumulated at an electrode and 2) the material is removed by chemical reaction or electrochemically at constant current with measurement of electrode potential. Historically for the analysis of metal ions, mercury ions were added to the test solution to form a mercury amalgam when reduced. Alternatively, an HMDE or MFE was used and the oxidizing agent added after amalgam formation. However, the toxicity of mercury and its compounds have all but precluded the present-day use of mercury. The accumulation is similar to that used in stripping voltammetry. The stripping potentiogram shows staircase curves of potential as a function of time. Frequently, the first derivative is displayed (dE/dt=f(t)), as this produces peak-shaped signals. The time between transitions (peaks) is proportional to the concentration of analyte in the test solution. The time between changes in potential in step 2 is related to the concentration of analyte in the solution.

Category (Class)

OWL Class
Imported fromA prefixed IRI defining this entry as a imported term. In OSW the prefix must be a registered imported ontology.<br>Definition: OWL Class	https://w3id.org/emmo/domain/characterisation-methodology/chameo#PotentiometricStrippingAnalysis

EmmoClass
Supercategories<br>Definition: Category (Class), OWL Class, EmmoClass	Voltammetry
Alternative label<br>Definition: EmmoClass	PSA [en]
metaclass<br>Definition: Category (Class), EmmoClass	EmmoClass

Graph

Attachments

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jsondata

rdf_type

"owl:Class"

uuid

"065e6243-e2a6-5835-8ce9-267455204750"

iri

"https://w3id.org/emmo/domain/characterisation-methodology/chameo#PotentiometricStrippingAnalysis"

name

"PotentiometricStrippingAnalysis"

label

text	"PotentiometricStrippingAnalysis"
lang	"en"

description

text

"Two-step electrochemical measurement in which 1) material is accumulated at an electrode and 2) the material is removed by chemical reaction or electrochemically at constant current with measurement of electrode potential. Historically for the analysis of metal ions, mercury ions were added to the test solution to form a mercury amalgam when reduced. Alternatively, an HMDE or MFE was used and the oxidizing agent added after amalgam formation. However, the toxicity of mercury and its compounds have all but precluded the present-day use of mercury. The accumulation is similar to that used in stripping voltammetry. The stripping potentiogram shows staircase curves of potential as a function of time. Frequently, the first derivative is displayed (dE/dt=f(t)), as this produces peak-shaped signals. The time between transitions (peaks) is proportional to the concentration of analyte in the test solution. The time between changes in potential in step 2 is related to the concentration of analyte in the solution."

lang

"en"