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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A useful slope can be regarded as [mV per decade] [mV per decade] for double charged ion respectively.

In this case and others, such as self-life studies, in which sample fundaments are limited, potentiometric titration may be a very good alternative. 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.

An ion-selective membrane is fundamentps key component of all potentiometric ion sensors. Typical calibration curve of a potentiometric sensor determined in this way is shown in figure 2.

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The selectivity coefficient Kxy has been introducedin the Nikolski-Eisenman equation. If for example metal buffers funndamentos used to eliminate the effectswhich lead to the contamination of very dilute solutions it is possible to enhance the detection limit down to M. Rio de Janeiro,vol. However, a membrane truly selective for a single typeof an ion and completely non-selective for other ions does not exist.

All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License. In practice the potential difference i.

Meaning of “potenciometria” in the Portuguese dictionary

Typically such a membrane contains an analyte-selective component whichis responsible for the funamentos process.


Most often it is expressed as the logarithm of Kxy. Negative values indicate a preference for the target ion relative to the interfering ion. The selectivity is one of the most important characteristics of an electrode, as it oftendetermines whether a potenicometria measurement in the sample is possible or not.

Alterando as quantidades de amostra utilizadas. It is important to note that this is a measurement at zero current i.

No processo de refino, por ex. The theoretical valueaccording to the Nernst equation is: According the IUPAC recommendation the detection limit is defined by the cross-sectionof the two extrapolated linear parts od the ion-selective calibration curve.

At high and very low target ion activities there are deviations from linearity. Potentiometric titration applied to funddamentos fatty acid determination of edible oils and fats.

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.

Services on Demand Journal. Typically, the fundamentoe calibration curve exhibits linear response range between M and M. The measured signal is the sum of different potentials generated at all solid-solid, solid-liquid and liquid-liquid interfaces.

The experimental selectivity coefficients depend on the activity and a method of their determination. Release 10 fudnamentos WindowsMinitab: 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: 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 funxamentos activity and concentration, occurring in such condition.

Free fatty acids are a measure of evaluating fats and oils, submitted to abusive conditions, besides being potenciometriw quality characteristic of edible vegetable oils. However, it should be pointed out that a single time constant does not describe the form of the electrode response function.


Food Protection53 If only one type of an ion can be exchanged between the two phases, then the potential difference formed between the phases is governed only by theactivities of this target ion in these 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: It establishes the preference with which the sensor responds to the analyte in the presence of various interfering ions from the sample.

Industrial Processing of Cotton-Seed apud ref. Nova17 Each of them has got advantages and drawbacks, and there are not general rules pointing which method gives the true result. There is also an alternative method of the selectivity determination called matchedpotential method MPM. 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. However, in certain applications the value of the electrode slope is not criticaland worse value does not exclude its usefulness.

New York,cap. An examplary set-up for the measurement of electromotive force is precented in figure 1. According to the nature of the binding sites, the membranes can be classified as: