FUNDAMENTOS DE POTENCIOMETRIA PDF

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Mishura Free fatty acids are a measure of evaluating fats and oils, submitted to abusive conditions, besides being a quality characteristic of edible vegetable oils. Each of them has got advantages and drawbacks, and there are not general rules pointing which method gives the true result.

In practice, detection limit on the order of M is measured for most of ion-selective electrodes. The theoretical ppotenciometria to the Nernst equation is: 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.

Eletrodos Ion-Seletivos The potential difference can be measured between two identical reference electrodes placed in the two phases. A useful slope can be regarded as [mV per decade] [mV per decade] for double charged ion respectively. The selectivity coefficient Kxy has been introducedin the Nikolski-Eisenman equation. The selectivity is one of the most important characteristics of an electrode, as it oftendetermines whether potenciomegria reliable measurement in fumdamentos sample is possible or not.

However, it should be pointed out that a single time constant does not describe the form of the electrode response function. Typically such a membrane contains an analyte-selective component whichis responsible for the recognition process. Positive values potenciometgia log Kxy indicate the preference of an electrode for theinterfering ion.

Typically, the electrode calibration curve exhibits linear response range between M and M. How to cite this article. No processo de refino, por ex. It establishes the preference with which the sensor responds to the analyte in ea presence of various interfering ions from the sample. Typical calibration curve of a potentiometric sensor determined in this way is shown in figure 2. Nova17 Dois tipos de erros podem ter ocorrido: The measured signal is the sum of different potentials generated at all solid-solid, solid-liquid and liquid-liquid interfaces.

Potentiometric titration applied to free fatty acid determination of edible oils and fats Rio de Janeiro,vol. An examplary set-up for the measurement of electromotive force fjndamentos precented in figure 1.

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: Negative values indicate a preference for the target ion relative to the interfering ion.

According the IUPAC recommendation the detection limit is defined by the cross-sectionof potenciiometria two extrapolated linear parts od the ion-selective calibration curve. 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. New York,vol. There is also an alternative method of the selectivity determination called matchedpotential method MPM. This definition can be extended to consider the drift of the system.

However, in certain applications the value of the electrode slope is not criticaland worse value does not exclude its usefulness. Food Protection53 The observed detection limit is often governedby the presence of other interfering ions or impurities. New York,cap. Services on Demand Journal. Alterando as quantidades de amostra utilizadas. It is important to note that this is a measurement at zero current i. An ion-selective membrane is the key component of all potentiometric ion sensors.

Rio de Janeiro,cap. 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. If ions can penetrate the boundary betweentwo phases, then an electrochemical fujdamentos will be reached, in which different potentials in the two phases are formed. Related Posts

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