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Diagnostic wavelengths

Although such instruments as described earlier are available, they are not typically used in soil analysis. Today, samples are most often aspirated into a flame or torch to cause the promotion of electrons in elements, and the diagnostic wavelengths are detected and quantified by photomultipliers. Modern spectrometers are different because of the use of many different ways of heating samples and the range of wavelengths available. Today, because of increased sensitivity of instrumentation and detectors, more of the spectrum is available for this type of analysis. Thus, wavelengths from 200 to 900 nm can be used for the analysis of the elements that are present. [Pg.306]

Raman infrared spectroscopy A particular wavelength from IR in the electromagnetic spectrum is projected onto a sample and the diagnostic wavelengths of the light scattered at a high angle are recorded. [Pg.272]

UV-VIS In the absence of any additional chromophores carboxylic acids absorb at a wavelength (210 nm) that is not very useful for diagnostic purposes... [Pg.821]

Fig. 4. Examples of emission spectrometry as a diagnostic monitoring tool for plasma processing, (a) The removal of chlorine contamination from copper diode leads using a hydrogen—nitrogen plasma. Emissions are added together from several wavelengths, (b) The etching and eventual removal of a 50-p.m thick polyimide layer from an aluminum substrate, where (x ) and (° ) correspond to wavelengths (519.82 and 561.02 nm, respectively) for molecular CO2... Fig. 4. Examples of emission spectrometry as a diagnostic monitoring tool for plasma processing, (a) The removal of chlorine contamination from copper diode leads using a hydrogen—nitrogen plasma. Emissions are added together from several wavelengths, (b) The etching and eventual removal of a 50-p.m thick polyimide layer from an aluminum substrate, where (x ) and (° ) correspond to wavelengths (519.82 and 561.02 nm, respectively) for molecular CO2...
Cahbration with standard reflectance and transmittance samples should be routinely used for optimum results in spectrophotometry and colorimetry. Cahbration of the wavelength (32) and photometric (33) scales is also advisable. The cahbration of a white reflectance standard in terms of the perfect reflecting diffuse, T, has been discussed (34), as have diagnostic tiles for tristimulus colorimetry (35). A collaborative reference program is available on instmment performance (36). [Pg.417]

Raman spectroscopy is primarily useful as a diagnostic, inasmuch as the vibrational Raman spectrum is directly related to molecular structure and bonding. The major development since 1965 in spontaneous, c.w. Raman spectroscopy has been the observation and exploitation by chemists of the resonance Raman effect. This advance, pioneered in chemical applications by Long and Loehr (15a) and by Spiro and Strekas (15b), overcomes the inherently feeble nature of normal (nonresonant) Raman scattering and allows observation of Raman spectra of dilute chemical systems. Because the observation of the resonance effect requires selection of a laser wavelength at or near an electronic transition of the sample, developments in resonance Raman spectroscopy have closely paralleled the increasing availability of widely tunable and line-selectable lasers. [Pg.466]

Quality assurance measures such as pre-analytical checks on instrumental stability, wavelength calibration, balance calibration, tests on resolution of chromatography columns, and problem diagnostics are not included. For present purposes they are regarded as part of the analytical protocol, and IQC tests their effectiveness together with the other aspects of the methodology. [Pg.87]

Between 1926 and 1962, numerous ORD curves of optically active sulfoxides were described in the literature for the visible and ultraviolet (UV) regions. However, down to about 250 nm all compounds investigated showed plain curves with [0] increasing toward shorter wavelengths, and this limited their diagnostic value for the determination of the absolute configuration of these compounds. [Pg.397]

Unlike MUR, PCR and PLS are methods that can be used without explicitly selecting variables. This is accomplished by transforming the measured variables (e.g., absorbance values at many wavelengths) into new variables (often referred to as factors) that are used in the matrix calculations. The difference between PCR and PLS is in how this variable transformation is performed. Both PCR and PLS have good diagnostic tools and in general the results are similar. These methods are often preferred over MLR unless the number of variables is small or circumstances dictate the explicit reduction in the number of varialj es. [Pg.99]

When an energetic electron scatters inelastically, an electron from the (filled) valence band can be promoted to the (empty) conduction band creating an electron/hole pair. On recombination, the excess energy is released as a photon, the wavelength of which is well defined by the band-gap transition. The technique is powerful in catalysis it is diagnostic of the electronic/chemical state and is sensitive to point defects. It can be used to probe the distribution of dopants in catalytic oxides. [Pg.74]


See other pages where Diagnostic wavelengths is mentioned: [Pg.306]    [Pg.307]    [Pg.307]    [Pg.251]    [Pg.195]    [Pg.368]    [Pg.370]    [Pg.306]    [Pg.307]    [Pg.307]    [Pg.251]    [Pg.195]    [Pg.368]    [Pg.370]    [Pg.429]    [Pg.721]    [Pg.821]    [Pg.235]    [Pg.235]    [Pg.8]    [Pg.374]    [Pg.464]    [Pg.126]    [Pg.160]    [Pg.46]    [Pg.290]    [Pg.510]    [Pg.28]    [Pg.126]    [Pg.160]    [Pg.175]    [Pg.489]    [Pg.89]    [Pg.199]    [Pg.65]    [Pg.3]    [Pg.31]    [Pg.63]    [Pg.4]    [Pg.16]    [Pg.292]    [Pg.141]    [Pg.106]    [Pg.213]    [Pg.506]    [Pg.14]    [Pg.1]    [Pg.21]   
See also in sourсe #XX -- [ Pg.289 ]




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