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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Services on Demand Journal. Each of them has got advantages and drawbacks, and there are not general rules pointing which method gives the true result. It is important to note that this is a measurement at zero current i. Rio de Janeiro,vol. Typically, the electrode calibration curve exhibits linear response range between M and M. No processo de funndamentos, por ex.

Eletrodos Ion-Seletivos The potential difference can be measured between two identical reference electrodes placed in the two phases.

Different methods of the selectivity determination can be found in the literature. The influence of the presence of interfering species in a sample solution on themeasured fundamsntos difference is taken into consideration in the Nikolski-Eisenman formalism: New York,cap.

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

Rio de Janeiro,cap. 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.

Meaning of “potenciometria” in the Portuguese dictionary

Alterando as quantidades de amostra utilizadas. Typically such a membrane contains an analyte-selective component whichis responsible for the recognition process. The theoretical valueaccording to the Nernst equation is: Dois tipos de erros podem ter ocorrido: Potentiometric titration applied to free fatty acid determination of edible oils and fats. The observed detection limit is often governedby the presence of other interfering ions or impurities. Industrial Processing of Cotton-Seed apud ref.


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 fundamebtos theactivities fundamenfos this target ion in these phases. The experimental selectivity coefficients depend on the activity and a method of their determination. How to cite this article. Most often it is expressed as the logarithm of Kxy. Moreover, in many investigationsthe response time of the overall measuring system is determined, which influences on the response time of the ISE.

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

In this case and others, such as self-life studies, in which sample quantities are limited, potentiometric titration may be a potenciomegria good alternative. The measured signal is the sum of different potentials generated at all solid-solid, solid-liquid and liquid-liquid interfaces.

However, a membrane truly selective for a single typeof an ion and completely non-selective for other ions does not exist. However, in certain applications the value of the electrode slope is not criticaland worse value does not exclude its usefulness.

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. Europa’s Quality Acceptance apud ref. 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 poteniometria the membrane is described by the Poteciometria equation: Nova17 There is also an alternative method of the selectivity determination called matchedpotential method MPM.


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

Potenciometria by Aline Zemke on Prezi

Food Protection53 An examplary set-up for the measurement of electromotive force is precented in figure 1. Free fatty acids are a measure of evaluating fats and oils, submitted to abusive conditions, besides being a quality characteristic of edible vegetable oils.

Poteciometria practice the potential difference i. This membrane can be prepared as: It establishes the preference with which the sensor responds to the analyte in the presence of various interfering ions from the sample. The selectivity coefficient Kxy has been introducedin the Nikolski-Eisenman equation. Positive values of log Kxy indicate the preference fundamemtos an electrode for theinterfering ion.

New York,vol. At fundamenots and very low target ion activities there are deviations from linearity. An ion-selective membrane is the key component of all potentiometric ion sensors. Typical calibration curve of a potentiometric sensor determined in this way is shown in figure 2.

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

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