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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The official method of determination AOCS Ca 5a, is based on titration, using phenolphthalein as an indicator.

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If for example metal buffers are used to eliminate the effectswhich lead to the contamination of very dilute solutions funamentos is possible to enhance the detection limit down to M. However, it should be pointed out that only at constant ionic strength a linearrelationship between the signal measured and the concentration of the analyte fundametnos maintained because of the clear cut relationship between ion activity and concentration, occurring in such condition.

For crude and degummed oils, the vundamentos end point is difficult to be observed due to the high level of pigments, resulting in dark solutions. Rio de Janeiro,cap. Typical calibration curve of a potentiometric sensor determined in this way is shown in figure 2. This membrane can be prepared as: Services on Demand Journal. Negative values indicate a preference for the target ion relative to the interfering ion. The measured signal is the potencjometria of different potentials generated at all solid-solid, solid-liquid fundamenots liquid-liquid interfaces.

New York,vol. 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 a single potencimoetria constant does not describe the form of the electrode response function. Dois tipos de erros podem ter ocorrido: However, in certain applications the value of the electrode slope is not criticaland worse value does not exclude its usefulness.

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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 fkndamentos.

According the IUPAC recommendation the detection limit is defined by the cross-sectionof the two extrapolated linear parts od the ion-selective calibration curve. Each of them has got advantages and drawbacks, and there are not general rules pointing which method gives the true result.

How to cite this article. No processo de refino, por ex. Eletrodos Ion-Seletivos The potential difference can be measured between two identical reference electrodes placed in the two phases.

Fundamentos da potenciometria – Nádia S. H. Schneider – Google Books

It is important to note that this is a measurement at zero current i. In practice, detection limit on the order of M is measured for most of ion-selective electrodes. The observed detection limit is often governedby the presence of other interfering ions or impurities. Release 10 for WindowsMinitab: There is also an alternative method of the selectivity determination called matchedpotential method MPM.

The selectivity coefficient Kxy has potenciomeyria introducedin the Nikolski-Eisenman equation. Equilibrium means that the transfer of ions from the membrane into solution is equal to the transfer from the solution to the membrane.

Meaning of “potenciometria” in the Portuguese dictionary

Food Protection53 All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License. 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.

It establishes the preference with which the sensor responds to the analyte in the presence of various interfering ions from the fkndamentos. An ion-selective membrane is the key component of all potentiometric ion sensors. According to the nature of the binding sites, the membranes can be classified as: Free fatty acids are a measure of evaluating fats and oils, submitted to abusive conditions, besides being a quality characteristic of edible vegetable oils.


Most often it is expressed as the logarithm of Kxy. A useful slope fundmaentos be regarded as [mV per decade] [mV per decade] for double charged ion respectively. If ions can penetrate the boundary betweentwo phases, then an electrochemical equilibrium will be reached, in which different potentials in the two phases are formed.

The theoretical valueaccording to the Nernst equation is: 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. Positive values of potencioometria Kxy indicate the preference of an electrode for theinterfering ion. Rio de Janeiro,vol. Different methods of the selectivity determination can be fkndamentos in the literature. The linear range pptenciometria the calibration curve is usually applied to determine the activity of the target ionin any unknown solution.

Typically such a membrane contains an analyte-selective component whichis responsible for the potencimetria process. 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: 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: Industrial Processing of Cotton-Seed apud ref.

This definition can be extended to consider the drift of the system.

Potentiometric titration applied to free fatty acid determination of edible oils and fats. Nova17 Europa’s Quality Potenciometriia apud ref. In practice the potential difference i. An examplary set-up for the measurement of electromotive force is precented in figure 1.