FUNDAMENTOS DA POTENCIOMETRIA PDF

Análise potenciométrica de redissolução com ultramicroeletrodos: fundamentos e aplicações na determinação de metais traços. Quím. Nova [online]. 09/02/ la química analítica es la parte de la química que estudia, diseña, desarrolla, optimiza y aplica métodos y técnicas que se materializan en. fundamentos fisioquímicos grado farmacia us métodos químicos: son todos aquellos que se basan casi exclusivamente en reacciones químicas en los que la.

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[Potencio & Conduto] Aula – Métodos Eletroquímicos e Titulação Potenciométrica (Guts)

If for example metal buffers are used to eliminate the effectswhich lead to the contamination of very dilute solutions it is possible to enhance the detection limit down to M. The selectivity is one of the most important characteristics of an electrode, as it oftendetermines whether a reliable measurement in the sample is possible or not.

Rio de Janeiro,cap. Each of them has got advantages and drawbacks, and there are not general rules pointing which method gives the true result. An examplary set-up for the measurement of electromotive force is precented in figure 1. The measured fundamntos is the sum of different potentials generated at all solid-solid, solid-liquid and liquid-liquid interfaces.

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A useful slope can be regarded as [mV per decade] [mV per decade] for double charged ion respectively. Dois tipos de erros podem ter ocorrido: Typically, the electrode calibration curve exhibits linear response range between M and M. In practice the potential difference i.

Services on Demand Journal. The selectivity coefficient Kxy has been introducedin the Nikolski-Eisenman equation. Industrial Processing of Cotton-Seed apud ref. According to the nature of the binding sites, the membranes can be classified as: Moreover, in many investigationsthe response time findamentos the overall measuring system is determined, which influences on the response time of the ISE.

Meaning of “potenciometria” in the Portuguese dictionary

Nova17 How to cite this article. However, it should be pointed out that only at constant ionic strength a linearrelationship between the signal measured and the concentration of potenciomstria analyte is maintained because of the clear cut relationship between ion activity and concentration, occurring in such condition. Release 10 for WindowsMinitab: New York,cap.

It establishes the preference with which the sensor responds to the analyte in the presence of various interfering ions from the sample. Typical calibration curve of potencioetria potentiometric sensor determined in this way is shown in figure 2.

Typically such a membrane contains an analyte-selective component whichis responsible for the recognition process. This membrane can be prepared as: It is important to note that this is a measurement at zero current i. The influence of the presence of interfering species in a sample solution on themeasured potential difference is taken into consideration in the Nikolski-Eisenman formalism: No processo de refino, por ex.

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For this reason the potential of sucha membrane is governed mainly by the activity of the primary target ion and ;otenciometria by the activity of othersecondary interfering ions. Europa’s Quality Acceptance apud ref. The linear range of the calibration curve is usually applied to determine the activity of the target ionin any unknown solution. According the IUPAC recommendation the detection limit is defined by the cross-sectionof the two extrapolated linear parts od the ion-selective calibration curve.

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This definition can be extended to consider the drift of the system. All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License. However, it funramentos be pointed out that a single time constant does not describe the form of the electrode response function. Rio de Janeiro,vol.

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