3 Fuente: D.A. Skoog, D.M. fundamentos de quimica analitica skoog pdf descargar gratis West, F.J. Holler, Fundamentos de Química Analítica, Editorial. Quimica. Skoog fundamentos de quimica analitica pdf Fundamentos de Química Analítica, Skoog, LIBRO PDF. Fundamentos de química analítica, novena edición, es un. Douglas a. Skoog, D. M. West, F. J. Holler – Ebook download as PDF File .pdf), Text File .txt) or read book online. libro de fundamentos de quimica analitica de Souglas a. Skoog Como Descargar La Contraseña. Cargado por.

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The absorbances of the three standards are analitiica to be 0. The unknown absorbance was approximately 0. From the analysis, the concentration of the unknown is 0. During drying and ashing, volatile absorbing species may have been formed.

In addition, particulate matter would appear as smoke during ashing, which would scatter source radiation and reduce its intensity.

This behavior results from the formation of nonvolatile complexes between calcium and phosphate. The suppressions levels off after a stoichiometric amount of phosphate has been added.

Solucionário livro Fundamentos de Química Analítica SKOOG

The interference can be reduced by adding a releasing agent which ties up the phosphate when added in excess. When an internal standard is used, the ratio of intensity of the analyte line to that of the internal standard is plotted as a function of the analyte concentration see Figure If the internal standard and the analyte species are influenced in the same way by variation in the aspiration rate and the flame temperature, and if the internal standard is present at approximately the same concentration in the standards and the unknown, the intensity ratio should be independent of these variables.

Principles of Instrumental Analysis, 6th ed. Chapter 9 7 Setting up two equations in two unknowns 0. In the spreadsheet below we first calculate the equation for the line in cells B10 and B G7, and the mean Na concentrations in cell D8: These values are uncorrected for the blank. The blank corrections are made in Cells B D15 by gundamentos following equation 22 6 conc. Since the final result is obtained by subtracting the blank reading, the standard deviations must be calculated from the difference in cells E Chapter 9 8 Principles of Instrumental Analysis, 6th ed.


Chapter 9 9 Principles of Instrumental Analysis, 6th ed. Chapter 9 9 An internal standard is a substance that responds to uncontrollable variables in a similar way as the analyte. It is introduced into or is present in both standards and samples in a fixed amount. The ratio of the analyte signal to the internal standard signal then serves as the analytical reading. Flame atomic absorption ed a separate lamp for fudamentos element, which is not convenient when multiple elements are to be determined.


In a plasma, the high concentration of electrons suppresses extensive ionization of the analyte. In the presence of air and with graphite electrodes, strong cyanogens CN bands desxargar the wavelength region of to nm of little use. By excluding nitrogen with an inert gas, the intensities of these bands are greatly reduced making possible detection of several elements with lines in this region.

By Nebulization, by electrothermal vaporization, and by laser ablation. Chapter 10 2 The advantages of the ICP over the Skopg are higher sensitivity for several elements and freedom from some interferences and maintainence problems. No electrodes need to be replaced in the ICP, whereas in the DCP, the graphite electrodes must be replaced every few hours. Advantages of the DCP include lower argon consumption and simpler and less expensive equipment.

Ionization interferences are less severe in the ICP than in flame emission because argon plasmas have a high concentration of electrons from ionization of the argon which represses ionization of the analyte.


Advantages of plasma sources include: Emission spectra for many elements can be obtained with one set of excitation conditions.

Resolução Skoog

Spectra can be obtained for elements that tend to form refractory compounds. Plasma sources usually have a linearity range that covers several decades in concentration.

The internal standard method is often used in preparing ICP calibration curves to compensate for random instrumental errors that arise from fluctuations in the output of znalitica plasma source. Three types of mass spectrometers are used in atomic mass spectrometry: The quadrupole mass spectrometer separates ions of different mass based on selective filtering of ions during their passage through four parallel rods that serve as electrodes.

One pair of rods is attached to a positive dc voltage and the other to a negative dc voltage. The ions to be separated are then accelerated between the rods.


All others are annihilated by stiking the rods. By varying the dc and ac voltages simultaneously, separation of ions of different masses occurs. In the time-of-flight mass spectrometer, ions are accelerated periodically into a field-free drift tube. Their velocity in the tube is determined by their mass-to-charge ratio so that they arrive at a detector at different times depending on their mass In a double-focusing mass spectrometer, ions are accelerated into a curved electrostatic field and then into an electromagnetic field.

The lightest ions are deflected to a greater fundammentos than are heavier ions, and thus are dispersed on a plane where they are detected. Posta de novo em rar para que possamos baixar.