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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Eletrodos Ion-Seletivos The potential difference can be measured between two identical reference electrodes placed in the two phases. According the IUPAC recommendation the detection limit is defined by the cross-sectionof the two extrapolated linear parts od the ion-selective calibration curve. Industrial Processing of Cotton-Seed funxamentos ref. Positive values of log Kxy indicate the preference of an electrode for theinterfering ion.

Potenciometrla, in many investigationsthe response time of the overall measuring system is determined, which influences on the response time of the ISE. Most often it is expressed as the logarithm of Kxy. The official method of determination AOCS Ca 5a, is based on titration, using phenolphthalein as an indicator.

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. It establishes the preference with which the sensor responds to the analyte in the presence of various interfering ions from the sample.

It is important to note that this is a measurement at zero current i. Alterando as quantidades de amostra utilizadas. 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 fundamentox will be reached, in which different potentials in the two phases are formed. 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.

Equilibrium means that the transfer of ions from the membrane into solution is equal to the transfer from the solution to the membrane. 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. All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License.

The experimental selectivity coefficients potencionetria on the activity and a method of their determination. New York,vol. Different methods of the sa determination can be found in the literature. Each of them has got advantages and drawbacks, and there are not general rules pointing which method gives the true result. In practice the potential difference i.

Potenciometria by Aline Zemke on Prezi

In practice, detection limit on the order of M is measured for most of ion-selective electrodes. This definition can be extended to consider the drift of the system. Typically such a membrane contains an analyte-selective component whichis responsible for the recognition process. 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.

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. Ra is also an alternative method of the selectivity determination called matchedpotential method MPM. However, it should be pointed out that a single time constant does fundwmentos describe the form of the electrode response function.


The measured signal is the sum of different potentials generated at all solid-solid, solid-liquid and liquid-liquid interfaces. New York,cap. The selectivity coefficient Kxy has been introducedin the Nikolski-Eisenman equation. Potentiometric titration applied to free fatty acid determination of edible oils and fats. Dois tipos de erros podem ter ocorrido: At high and very low target ion activities there are deviations from linearity.

Meaning of “potenciometria” in the Portuguese dictionary

Rio de Janeiro,cap. Release 10 for WindowsMinitab: A useful slope can be regarded as [mV per decade] [mV per decade] for double charged ion respectively.

Rio de Janeiro,vol. Nova17 Typically, the electrode calibration curve exhibits linear response range between M and M. Typical calibration curve of a potentiometric sensor determined in this way is shown potenciometrla figure 2.

According to the nature of the binding sites, the membranes can be classified as: Potehciometria Protection53 The theoretical valueaccording to the Nernst equation is: The observed detection limit is often governedby the presence of other interfering ions or impurities.

However, a membrane truly selective for a single typeof an ion and completely non-selective for other ions does not exist. 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: