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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Release 10 for WindowsMinitab: According the IUPAC recommendation the detection limit is defined by the cross-sectionof the two extrapolated linear parts od the ion-selective calibration curve. Typically such a membrane contains an analyte-selective component whichis responsible for the recognition process.

The experimental selectivity coefficients depend on the activity and a method of their determination. In this case and others, such as self-life studies, in which sample quantities are limited, potentiometric titration may be a very good alternative.

An ion-selective membrane is the key component of all potentiometric ion sensors. Food Protection53 Positive values of log Kxy pofenciometria the preference of an electrode for theinterfering ion.

Typically, the electrode calibration curve exhibits linear response range between M and M. The official method of determination AOCS Ca 5a, is based on titration, using phenolphthalein as an indicator.

Industrial Processing of Cotton-Seed apud ref.

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: Free fatty acids are a measure of evaluating fats and oils, submitted to abusive optenciometria, besides being a 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.


Potencioemtria de Janeiro,cap.

Meaning of “potenciometria” in the Portuguese dictionary

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. Nova17 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 potenckometria target ion in these phases.

Fubdamentos definition can be extended to consider the drift of the system. According to the nature of the binding sites, the membranes can be classified as: Moreover, in many investigationsthe response time of the overall measuring system is determined, which influences on potenciomrtria response time of the ISE.

Services on Demand Journal. 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. Potenciometfia theoretical valueaccording to the Nernst equation is: The selectivity coefficient Kxy has been introducedin the Nikolski-Eisenman equation. 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.

In practice the potential difference i. In practice, detection limit on the order of M is measured for most of ion-selective potenciomehria. 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.


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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 the analyte is maintained because of the clear cut relationship between ion activity and concentration, occurring in such condition. Different methods of the selectivity determination can be found in the literature. An examplary set-up for the measurement of electromotive force is precented in figure 1.

There is also an alternative method of the selectivity determination called matchedpotential method MPM. However, in certain applications the value of the electrode slope is not criticaland worse value does not exclude its usefulness. Negative values indicate a preference for the target ion relative to the interfering ion. At high and very low target ion activities there are deviations fundxmentos linearity.

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