Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Atomic optical emission spectroscopy instrumentation

Multielement analysis will become more important in industrial hygiene analysis as the number of elements per sample and the numbers of samples increases. Additional requirements that will push development of atomic absorption techniques and may encourage the use of new techniques are lower detction and sample speciation. Sample speciation will probably require the use of a chromatographic technique coupled to the spectroscopic instrumentation as an elemental detector. This type of instrumental marriage will not be seen in routine analysis. The use of Inductively Coupled Plasma-Optical Emission Spectroscopy (ICP-OES) (17), Zeeman-effect atomic absorption spectroscopy (ZAA) (18), and X-ray fluorescence (XRF) (19) will increase in industrial hygiene laboratories because they each offer advantages or detection that AAS does not. [Pg.263]

Gravimetric methods and chemical methods, such as colorimetric measurements based on the arsenic-molybdenum blue complex (1,2,3) and arsine generation in combination with silver diethyldithiocarbamate (4, 5, 6,7), have been used to measure arsenic in aqueous media. Various instrumental methods such as differential pulse polarography (8), heated vaporization atomic absorption (9), arsine generation in combination with atomic absorption spectroscopy (10, 11, 12) or non-dispersive atomic fluorescence spectroscopy (13), and optical emission spectroscopy (14) can be used to determine arsenic in aqueous solutions. [Pg.63]

Because light emitted from inductively coupled plasma torches is characteristic of the elements present, the torches were originally introduced for instruments that optically measured the frequencies and intensities of the emitted light and used them, rather than ions, to estimate the amounts and types of elements present (inductively coupled plasma atomic emission spectroscopy. [Pg.87]

Numerous methods have been published for the determination of trace amounts of tellurium (33—42). Instrumental analytical methods (qv) used to determine trace amounts of tellurium include atomic absorption spectrometry, flame, graphite furnace, and hydride generation inductively coupled argon plasma optical emission spectrometry inductively coupled plasma mass spectrometry neutron activation analysis and spectrophotometry (see Mass SPECTROMETRY Spectroscopy, OPTICAL). Other instrumental methods include polarography, potentiometry, emission spectroscopy, x-ray diffraction, and x-ray fluorescence. [Pg.388]

With the exception of better optical resolution needed, the basic instrument used for atomic emission is very similar to that used for atomic absorption with the difference that no primary light source is used for atomic emission. One of the most critical components for this technique is the atomisation source because it must also provide sufficient energy to excite the atoms as well as atomise them. The earliest energy sources for excitation were simple flames, but these often lacked sufficient thermal energy to be truly effective sources. The development in 1963 and the introduction in 1970 of the first commercial inductively coupled plasma (ICP) as a source for atomic emission dramatically changed the use and the utility of emission spectroscopy (Thompson Walsh 1983). [Pg.81]

Several instrument manufacturers offer echelle-lype spectrometers for simultaneous determination of a multitude of elements by atomic emission spectroscopy. The optical designs of two of these instruments are shown in Figures 10-7,10-9, and 10-11. [Pg.630]

Since the introduction of the first commercially available atomic absorption spectrophotometer (AAS) in the early 1960s, there has been an increasing demand for better, faster, easier-to-use, and more flexible trace element instrumentation. A conservative estimate shows that today s market for atomic spectroscopy (AS)-based instruments, such as atomic absorption (AA), inductively coupled plasma optical emission (ICP-OES), and inductively coupled plasma mass spectrometry (ICP-MS), represents over 700 million in annual revenue. After market sales and service costs are added to this number, it is probably close to 1 billion. As a result of this growth, we have seen a rapid emergence of more sophisticated equipment and easier-to-use software. Moreover, with an increase in the number of manufacturers of both instrumentation and sampling accessories, the choice of which technique to use is often unclear. [Pg.241]

The besl isolation of radiant energy can he achieved with flame spectrometers that incorporate either a prism sir grating monochromator, those with prisms having variable gauged entrance and exii slits. Both these spectrometers provide a continuous selection of wavelengths with resolving power sufficient lo separate completely most of the easily excited emission lines, and afford freedom from scattered radiation sufficient lo minimize interferences. Fused silica or quartz optical components are necessary to permit measurements in Ihe ultraviolet portion of the spectrum below 350 nanometers Sec also Analysis (Chemical) Atomic Spectroscopy Photometers and Spectra Instruments. [Pg.638]

Atomic spectroscopy is the oldest instrumental elemental analysis principle, the origins of which go back to the work of Bunsen and Kirchhoff in the mid-19th century [1], Their work showed how the optical radiation emitted from flames is characteristic of the elements present in the flame gases or introduced into the burning flame by various means. It had also already been observed that the intensities of the element-specific features in the spectra, namely the atomic spectral lines, changed with the amount of elemental species present. Thus the basis for both qualitative and quantitative analysis with atomic emission spectrometry was discovered. These discoveries were made possible by the availability of dispersing media such as prisms, which allowed the radiation to be spectrally resolved and the line spectra of the elements to be produced. [Pg.373]

See also Atomic Absorption Spectrometry Principles and Instrumentation Interferences and Background Correction Flame Electrothermal. Atomic Emission Spectrometry Principles and Instrumentation Flame Photometry. Elemental Speciation Practicalities and Instrumentation. Laser-Based Techniques. Optical Spectroscopy Radiation Sources Detection Devices. [Pg.238]


See other pages where Atomic optical emission spectroscopy instrumentation is mentioned: [Pg.285]    [Pg.263]    [Pg.285]    [Pg.62]    [Pg.897]    [Pg.151]    [Pg.428]    [Pg.151]    [Pg.799]    [Pg.76]    [Pg.152]    [Pg.18]    [Pg.24]    [Pg.309]    [Pg.1554]    [Pg.1555]    [Pg.1570]    [Pg.1573]    [Pg.1599]    [Pg.118]    [Pg.602]    [Pg.99]    [Pg.102]    [Pg.427]    [Pg.311]    [Pg.94]    [Pg.256]    [Pg.431]    [Pg.80]    [Pg.157]    [Pg.13]    [Pg.920]    [Pg.170]   


SEARCH



Atom optics

Atomic emission

Atomic emission spectroscopy

Atomic optical emission spectroscopy

Atomic spectroscopy

Emission spectroscopy)

Instrument optics

Instrumentation atomic emission spectroscopy

Instruments spectroscopy

Optical Instruments

Optical atomic spectroscopy

Optical emission

Optical spectroscopy

Spectroscopy instrumentation

© 2024 chempedia.info