Flame atomic emission

FLAME ATOMIC EMISSION, FLAME ATOMIC ABSORPTION,... 

The detection limits in the table correspond generally to the concentration of an element required to give a net signal equal to three times the standard deviation of the noise (background) in accordance with lUPAC recommendations. Detection limits can be confusing when steady-state techniques such as flame atomic emission or absorption, and plasma atomic emission or fluorescence, which... 

Flame Sources Atomization and excitation in flame atomic emission is accomplished using the same nebulization and spray chamber assembly used in atomic absorption (see Figure 10.38). The burner head consists of single or multiple slots or a Meker-style burner. Older atomic emission instruments often used a total consumption burner in which the sample is drawn through a capillary tube and injected directly into the flame. 

Method for background correction in flame atomic emission. 

Description of Method. Salt substitutes, which are used in place of table salt for individuals on a low-sodium diet, contain KCI. Depending on the brand, fumaric acid, calcium hydrogen phosphate, or potassium tartrate also may be present. Typically, the concentration of sodium in a salt substitute is about 100 ppm. The concentration of sodium is easily determined by flame atomic emission. Because it is difficult to match the matrix of the standards to that of the sample, the analysis is accomplished by the method of standard additions. 

Sensitivity Sensitivity in flame atomic emission is strongly influenced by the temperature of the excitation source and the composition of the sample matrix. Normally, sensitivity is optimized by aspirating a standard solution and adjusting the flame s composition and the height from which emission is monitored until the emission intensity is maximized. Chemical interferences, when present, decrease the sensitivity of the analysis. With plasma emission, sensitivity is less influenced by the sample matrix. In some cases, for example, a plasma calibration curve prepared using standards in a matrix of distilled water can be used for samples with more complex matrices. 

Instrumentation. Flame Characteristics. Flame Processes. Emission Spectra. Quantitative Measurements and Interferences. Applications of Flame Photometry and Flame Atomic Emission Spectrometry. 

Applications of Flame Photometry and Flame Atomic Emission Spectrometry... 

Operating Principles — There are many similarities between ICP-AES and the combustion flame spectroscopy techniques of flame atomic emission (FAE) and flame atomic absorption (FAA). In fact, the source of the ICP-AES has been referred to by Fassel as an electric flame. The final prepared analytical sample is presented in liquid form for analysis except for unique situations. The liquid sample is drawn (or... 

Analytical Techniques Atomic absorption spectrometry, 158, 117 multielement atomic absorption methods of analysis, 158, 145 ion microscopy in biology and medicine, 158, 157 flame atomic emission spectrometry, 158, 180 inductively coupled plasma-emission spectrometry, 158, 190 inductively coupled plasma-mass spectrometry, 158, 205 atomic fluorescence spectrometry, 158, 222 electrochemical methods of analysis, 158, 243 neutron activation analysis, 158, 267. 

In the past, flames used for atomic absorption spectrometry have also been used for atomic emission spectrometry, and these are described in some detail in Chapter 2. However, the advent of plasma excitation sources has resulted in the demise of flame atomic emission spectrometry, for the reasons discussed in Section 4.2.3. 

A wide range of instrumentation may be employed for flame atomic emission spectrometry, from filter photometers to highly sophisticated... 

D. The measurement of Li in brine (salt water) is used by geochemists to help determine the origin of this fluid in oil fields. Flame atomic emission and absorption of Li are subject to interference by scattering, ionization, and overlapping spectral emission from other elements. Atomic absorption analysis of replicate samples of a marine sediment gave the results in the table below. 

X-ray fluorence spectrometry was performed by P. A. Pella and flame atomic emission spectrometry by T. A. Butler, both of the NIST Analytical Chemistry Division. 

Flames (temperatures from 1700°C to 3100°C) and plasmas (temperatures ranging between 4000°C and 6000°C) are very efficient means of atomization they are used in FAAS, flame atomic emission spectrometry (FAES), ICP-OES, and ICP-MS. High temperatures (up to 3000°C) can also be obtained if an intense electrical current is set up between two electrical contacts. This type of atomization by electrical heating (electrothermal atomization) is the basis of ETA AS. 

Ba14C03 = radiolabeled barium carbonate EDTA = ethylenediamine tetraacetic acid FAAS = flame atomic absorption spectroscopy FAES = flame atomic emission... 

For instance, those elements present at relatively high concentration levels in milk are usually determined by FAAS or flame atomic emission spectrometry (FAES). On the other hand, if better LoDs are needed (e.g., ng g-1), the technique of choice would be ET-AAS. For multielemental analysis plasma-based techniques are recommended, such as AES for major elements and trace elements, or, as described below, mass spectrometry (MS) for major, trace, and ultratrace elements. The most relevant applications of these atomic techniques for elemental analysis in milk samples are summarized in Table 13.7. 

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