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results
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rdfs:comment is obtained. Peak current depends on time of, accumulation, mass transport of analyte (stirring), scan,AdSV is usually employed for analysis of organic @enhttps://w3id.org/emmo#EMMO_967080e5_2f42_4eb2_a3a9_c58143e835f9 by adsorption of the analyte (in contrast to @en
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rdfs:comment Coulometry used to measure the amount of, for a quantity of the same kind (i.e. amount of substance). @enhttps://w3id.org/emmo#EMMO_967080e5_2f42_4eb2_a3a9_c58143e835f9 laws of electrolysis, the amount of substance is proportional to the charge @en
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rdfs:comment mechanically enforced end of the drop. The pulse width is, usually 10 to 20 % of the drop time. The drop,, which is carried out just before the end of the pulse, as in NPV. @enhttps://w3id.org/emmo#EMMO_967080e5_2f42_4eb2_a3a9_c58143e835f9 voltammetry in which potential pulses of, pulse width of 2 to 200 ms are superimposed on a constant initial potential @en
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rdfs:comment (electrode current I which is usually a function of time – see chronoamperometry)., to the concentration of an electroactive analyte.,The integral of current with time is the electric @enhttps://w3id.org/emmo#EMMO_967080e5_2f42_4eb2_a3a9_c58143e835f9 distinguish selectively between a number of, of the applied potential and/or choice of electrode material. @en
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rdfs:comment investigation of mechanisms of electrochemi- cal, potential of the analyte reaction., positive limit of the cycle but can have any value @en
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rdfs:comment current is zero and the con- centrations of all, proportional to the logarithm of the activity, (concentration) of the analyte in the solution @enhttps://w3id.org/emmo#EMMO_967080e5_2f42_4eb2_a3a9_c58143e835f9 electrochemical potentials of a metallic structure in a given environment. @en
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rdfs:comment historically used to measure concentrations of metal ions in, to form an amalgam. Due to the toxicity of,, often sacrificing the probing of speciation and @enhttps://w3id.org/emmo#EMMO_967080e5_2f42_4eb2_a3a9_c58143e835f9 amount of an accumulated species is measured by, 2 is related to the concentration of analyte in @en
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rdfs:comment intersection of linear parts of the conductance G, versus titrant volume V, curve (see, of the analyte with another species, cor @enhttps://w3id.org/emmo#EMMO_967080e5_2f42_4eb2_a3a9_c58143e835f9 titration in which the electric conductivity of a, solution is measured as a function of the amount of titrant added @en
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rdfs:comment based on the integration of the I-t curve, of the transient can be detected more accurately, charge passed as a function of time can be @enhttps://w3id.org/emmo#EMMO_967080e5_2f42_4eb2_a3a9_c58143e835f9 of a potential step perturbation is measured as a function of time (Q-t curve) @en
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rdfs:comment Mass transport of a redox species enhanced by, either of the solution (solution stirring, or, channel flow), or of the electrode (electrode rotation or vibration). @enhttps://w3id.org/emmo#EMMO_967080e5_2f42_4eb2_a3a9_c58143e835f9 voltammetry with forced flow of the solution towards the electrode surface @en