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Infrared signal

Detection of the infrared signal is, of course, of prime importance. A range of detectors is available for this purpose, the type used in any particular instrument depending upon the type and quality of the spectrophotometer. [Pg.746]

Usually the infrared signal is modulated at a frequency /, and the responsivity of the bolometer decreases when G < 2irf x C, where C is the heat capacity of the bolometer. The optimum NEP occurs when G 2tt/ x C [74],... [Pg.339]

The use of infrared spectroscopy of adsorbed molecules to probe oxide surfaces has been reviewed by Davydov and Rochester [23], This approach works on sulfide catalysts as well. The infrared signal of NO has been successfully used to identify sites on the surface of a hydrodesulfurization catalyst, as the following example shows [24]. [Pg.229]

Infrared signals that corresponds to these intermediates, however, are so small except linearly adsorbed CO that it is difficult to judge the feasibility of these schemes. [Pg.112]

These intermediates are still questionable because the infrared signals are weak and they have not been confirmed yet by other groups. [Pg.115]

An interesting method of detecting infrared signals with sensitive and fast visible photomultipliers has been demonstrated by Boyd et al. The authors used the frequency mixing of infrared signals with visible light (10.6 yt COj laser with 0.6328 y He-Ne laser) in nonlinear crystals to produce the difference frequency wave ( at X = 0.6729 y) which can be detected by an S 20 photomultiplier. No additional source of noise due to the mixing process was observed. [Pg.59]

Figure 6 Transient infrared kinetics risetime for injected electrons originating from visible excitation (590 nm) Ru(4,4,-(COOH)2-2,2 -bipyridine)2(NCS)2 absorbed on nanostructured Ti02 thin films. The filled points arise from the infrared transient absorption at 5.4 pm, while the open points represent the single-sided VIS-IR cross correlation. An upper limit for the injection risetime is 350 fs. The horizontal arrow indicates the level of infrared signal induced by two-photon excitation of the substrate. Figure 6 Transient infrared kinetics risetime for injected electrons originating from visible excitation (590 nm) Ru(4,4,-(COOH)2-2,2 -bipyridine)2(NCS)2 absorbed on nanostructured Ti02 thin films. The filled points arise from the infrared transient absorption at 5.4 pm, while the open points represent the single-sided VIS-IR cross correlation. An upper limit for the injection risetime is 350 fs. The horizontal arrow indicates the level of infrared signal induced by two-photon excitation of the substrate.
However, Rest and co-workers (84) showed that irradiation of CpFe(CO)2CH3 at high dilution in CO matrices at 12 K gave rise to infrared signals which they attributed to the new species (tj -C5H5)Fe(CO)3CH3. No evidence for the species CpFe(CO)CH3 was found. The authors concluded that irradiation of the starting alkyl complex... [Pg.297]

Temporal monitoring resulted in the first direct evidence for active silicate volcanism on lo, when a large increase in lo s infrared signal was detected one night in 1986 in multiple spectral bands. Analysis of this event suggested that material with a temperature of > 900 K is necessary to explain the infrared spectral signature, ruling out molten sulfur (Johnson et al., 1988). [Pg.635]

FIG. 11.24 Beams arrangement at the prism output The two observed green signals are placed symmetrically aside the infrared signal. [Pg.358]

Hexadecanethiol monolayers also self-assemble on mercury surfaces and provide an extremely low defect density . Alkanethiols can likewise be assembled on GaAs (100) surfaces and can act as a useful semiconductor. Alkaneni-triles bind side-on (= x ) to gold and copper surfaces. The infrared signal in the range of 2000-2500 cm Ms replaced by a 1570-1630 cm band which is close to x -coordinated nitrile on platinum. Molecular dynamics calculations for —SH and —SCF13 on gold produced two chemisorption modes very close in energy . [Pg.161]

The kinetic equations for this simple sequential reaction can be solved analytically and the rate depends on two rate constants, and (see Scheme 1.2). The value of k is measured independently by similarly monitoring the time dependence of the intensity of the ethylidyne infrared signal of an initially ethylidyne-covered surface in the presence of hydrogen using infrared spectroscopy [69]. [Pg.13]


See other pages where Infrared signal is mentioned: [Pg.416]    [Pg.158]    [Pg.538]    [Pg.230]    [Pg.338]    [Pg.327]    [Pg.10]    [Pg.26]    [Pg.161]    [Pg.162]    [Pg.282]    [Pg.23]    [Pg.105]    [Pg.247]    [Pg.523]    [Pg.236]    [Pg.101]    [Pg.103]    [Pg.175]    [Pg.215]    [Pg.229]    [Pg.347]    [Pg.32]    [Pg.79]    [Pg.387]    [Pg.388]    [Pg.241]    [Pg.222]    [Pg.223]    [Pg.12]    [Pg.177]    [Pg.280]    [Pg.512]    [Pg.513]    [Pg.274]   


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