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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All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License. New York,vol.

Meaning of “potenciometria” in the Portuguese dictionary

However, a membrane truly selective for a single potenciomteria an ion and completely non-selective for other ions does not exist. Typically, the electrode calibration curve exhibits linear response range between M and M. For this reason the potential of sucha membrane is governed mainly by the activity of the primary target ion and also by the activity of othersecondary interfering ions.

Most often it is expressed as the logarithm of Kxy. Each of them has got advantages and drawbacks, and there are not general fundamentls pointing which method gives the true result. Release 10 for WindowsMinitab: Different methods of the selectivity determination can be found in the literature. However, in certain applications the value of the electrode slope is not criticaland worse value does not exclude its usefulness. Europa’s Quality Acceptance apud ref. Nova17 Alterando funadmentos quantidades de amostra utilizadas.

It establishes the preference with which the sensor responds to the analyte in the presence of various interfering ions from the sample. This potenclometria can be extended to consider the drift of the system.

Dois tipos de erros podem ter ocorrido: The linear range of the calibration curve is usually applied to determine the activity of the target ionin any unknown solution. Services on Demand Journal. If ions can penetrate the boundary betweentwo phases, then an electrochemical equilibrium will be reached, in which different potentials in fubdamentos two phases are formed.


In practice the potential difference i.

No processo de refino, por ex. For crude and degummed oils, the titration end point is difficult to be observed due to the high level of pigments, resulting in dark solutions.

Food Protection53 Eletrodos Ion-Seletivos When the membrane separates two solutions of different ionic activities a1 and a2 and provided the membrane is only permeable to this single type of ion, the potential difference E across the membrane is described by the Nernst equation: How to cite this article. New York,cap. 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.

Negative values indicate a preference for the target ion relative to the interfering ion. Typically such a membrane contains an analyte-selective component whichis responsible for the recognition process. The official method of determination AOCS Ca 5a, is based on titration, using phenolphthalein as an indicator. Free fatty acids are a measure of evaluating fats and oils, submitted to abusive conditions, besides being a ca characteristic of edible vegetable oils. There is also an alternative method of the selectivity determination called matchedpotential method Ffundamentos.

Eletrodos Ion-Seletivos The potential difference can be measured between two identical reference electrodes placed in the two phases. 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: However, it should be pointed out that a single time constant does not describe the form of the electrode response function.

The theoretical valueaccording to the Nernst equation is: Rio de Janeiro,vol.

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In this case and others, such as self-life studies, in which sample quantities are limited, potentiometric titration may be a very good alternative. The selectivity coefficient Kxy has been introducedin the Nikolski-Eisenman equation.


It is important to note that this is a measurement at zero current i. Rio de Janeiro,cap. Moreover, in many investigationsthe response time of the overall measuring system is determined, which influences on the response time of the ISE. However, it should be pointed out that only at constant ionic strength a linearrelationship between the signal measured and the concentration of the analyte is maintained because of the clear cut relationship between ion activity and concentration, occurring in such condition.

The experimental selectivity coefficients depend on the activity and a method of their determination. Potentiometric titration applied to free fatty acid determination of edible oils and fats. A useful slope can be regarded as [mV per decade] [mV per decade] for double charged ion respectively.

At high and very low target ion activities there are deviations from linearity. The observed detection limit is often governedby the presence of other interfering ions or impurities.

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According to the nature of the binding sites, the membranes can be classified as: According the IUPAC recommendation the detection limit is defined by the cross-sectionof the two extrapolated linear parts od the ion-selective calibration curve.

An ion-selective potencioemtria is the key component of all potentiometric ion sensors. 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.