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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Rio de Janeiro,vol.

It is important to note that this is a measurement at zero current i. Nova17 New York,vol.

If for example metal buffers fundamehtos used to eliminate the dundamentos lead to the contamination of very dilute solutions it is possible to enhance the detection limit down to M. Each of them has got advantages and drawbacks, and there are not general rules pointing which method gives the true result.

The theoretical valueaccording potwnciometria the Nernst equation is: The official method of determination AOCS Ca 5a, is based on titration, using phenolphthalein as an indicator. This membrane can be prepared as: Rio de Janeiro,cap. 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.

The selectivity is one of the most potencoometria characteristics of an electrode, as it oftendetermines whether a reliable measurement in the sample is possible or not. In this case and others, such as self-life studies, in which sample ptoenciometria are limited, potentiometric titration may be a very good alternative.

Alterando as quantidades de amostra utilizadas. Most often it is expressed as the logarithm of Kxy. Different methods of the selectivity determination can be found in the literature. 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. No processo de refino, por ex.


Services on Demand Journal. At potenxiometria and very low target ion activities there are deviations from linearity. How to cite this article.

According to the nature of the binding sites, the membranes can be classified as: It establishes the preference with which the sensor responds to the analyte in the presence of various interfering ions from the sample. Moreover, in many investigationsthe response time of the overall measuring system is determined, which influences on the response time of the ISE.

Europa’s Quality Acceptance apud ref. According the IUPAC recommendation the detection limit is defined by the cross-sectionof the two extrapolated linear parts od the ion-selective calibration curve.

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 ad activity and concentration, occurring in such condition.

The measured signal is the sum of different potentials generated at all solid-solid, solid-liquid and liquid-liquid interfaces.

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: The linear range of the calibration curve is usually applied to determine the activity of the target ionin any unknown solution.

Potentiometric titration applied to free fatty acid determination of edible oils and fats.

Potentiometric titration applied to free fatty acid determination of edible oils and fats

Eletrodos Ion-Seletivos When potenciomwtria membrane separates two solutions of poteenciometria 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: Free fatty acids are a measure of evaluating fats and oils, submitted to abusive conditions, besides being a quality characteristic of edible vegetable oils.

Equilibrium means that the transfer of ions from the membrane into solution is equal to the transfer from the solution to the membrane. An examplary set-up for the measurement of electromotive force is precented in figure 1.


Release 10 for WindowsMinitab: However, in certain applications the value of the electrode slope is not criticaland worse value does not exclude its usefulness. New York,cap.

All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License. Typically, the electrode calibration curve exhibits linear response range between M and M. The experimental selectivity coefficients depend on the activity and a method of their determination.

Industrial Processing of Cotton-Seed apud ref.

[Potencio & Conduto] Aula – Métodos Eletroquímicos e Titulação Potenciométrica (Guts)

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

This definition can be extended to consider the drift of the system. 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 fundamenttos phases are formed.

Dois tipos de erros podem ter ocorrido: Eletrodos Ion-Seletivos The potential difference can be measured between two identical reference electrodes placed in the two phases. However, a membrane truly selective for a single typeof an ion and completely non-selective for other ions does not exist. Positive values of log Kxy indicate the preference of an electrode for theinterfering ion.

There is also an alternative method of the selectivity determination called matchedpotential method MPM. Typically such a membrane contains an analyte-selective component whichis responsible for the recognition process.

Negative values indicate a preference for the target ion relative to the interfering ion. An ion-selective membrane is the key component of all potentiometric ion sensors.