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Infrared beam

If the sample is placed in the path of the infrared beam, usually between the source and the monochromator, it will absorb a part of the photon energy having the same frequency as the vibrations of the sample molecule s atoms. The comparison of the source s emission spectrum with that obtained by transmission through the sample is the sample s transmittance spectrum. [Pg.57]

Transmission, Absorption, and Beer s Law. The majority of infrared spectrometry is stiU done by the classic method of transmission spectrometry the intensity of an infrared beam passing completely through a sample is measured. The standard description of how much radiation passes through the sample is that of Beet s law (or the Bouguer-Beer-Lambertlaw) ... [Pg.197]

Attenuated total reflection (ATR), also called internal reflection, is based on the phenomenon of total internal reflection. In ATR the infrared beam is directed into an infrared-transmitting crystal so that it strikes the crystal surface at less than the critical angle and undergoes total internal reflection. [Pg.199]

In the Lasentec instruments a chord-length distribution is generated, from a rotating infrared beam, and this is converted to a size distribution. Since highly concentrated systems can be interrogated this system can be used for on-hne size analysis. [Pg.1827]

Figure 3 Typical beam path configuration for collecting an FTIR spectrum using an attenuated total reflectance element Iq is the incident infrared beam, f is the exiting beam. Figure 3 Typical beam path configuration for collecting an FTIR spectrum using an attenuated total reflectance element Iq is the incident infrared beam, f is the exiting beam.
In the gas correlation techniques, gas-filled cells mounted on a rotating disk cross the analyzing infrared beam in turn. One correlation cell is filled with a gas that will not absorb infrared light, such as nitrogen (N2). The other cell (or cells) are filled with a high concentration of the gas to be measured. The wavelength range is selected at the absorption band of the gas to be measured by an optical band-pass filter. [Pg.1297]

When measuring CO concentration, the reference signal is obtained when the beam is passed through the sample chamber and the CO cell. The absorption is then saturated due to the high CO concentration in the cell. Consequently, the reference signal is practically nondependent on the CO concentration in the sample gas. When the beam passes through the sample chamber and the N2 filter, the absorption is dependent on the CO concentration in the sample chamber, as the N2 filter does not absorb energy from the infrared beam. [Pg.1297]

An infrared beam is directed through a crystal of refractive index (ni) onto a sample of smaller refractive index (n2). The intensity of the reflected beam is monitored as a function of the wavelength of the incident beam. These absorptions are used to identify the chemical structure. ATR has a sampling depth of about 0.3-3.0 microns. [Pg.517]

There is limited application for CO trim systems which are widely used on utility and other large water-tube boilers. The principle of operation is for an infrared beam to traverse the flue from emitter to sensor. The absorption of the infrared radiation is proportional to the CO content. [Pg.278]

The thermocouple is made by welding together two wires of metals 1 and 2 in such a manner that a segment of metal 1 is connected to two terminal wires of metal 2. One junction between metals 1 and 2 is heated by the infrared beam, and the other junction is kept at constant temperature small changes in ambient temperature are thus minimised. To avoid losses of energy by convection, the couples are enclosed in an evacuated vessel with a window transparent to infrared radiation. The metallic junctions are also covered with a black deposit to decrease reflection of the incident beam... [Pg.746]

A bolometer is essentially a thin blackened platinum strip in an evacuated glass vessel with a window transparent to the infrared rays it is connected as one arm of a Wheatstone bridge, and any radiation absorbed raises the temperature of the strip and changes its resistance. Two identical elements are usually placed in the opposite arms of a bridge one of the elements is in the path of the infrared beam and the other compensates for variations in ambient temperature. Both the above receptors give a very small direct current, which may be amplified by special methods to drive a recorder. [Pg.746]

Infrared spectra for solid organic compounds are frequently obtained by mixing and grinding a small sample of the material with specially dry and pure potassi um bromide (the carrier), then compressing the powder in a special metal die under a pressure of 15 30 tonnes to produce a transparent potassium bromide disc. As the potassium bromide has virtually no absorption in the middle-infrared region, a very well-resolved spectrum of the organic compound is obtained when the disc is placed in the path of the infrared beam. [Pg.755]

Experimental design Groups of 12 male NMRI mouse pups were treated by gavage with 0, 50, or 290 mg/kg/day trichloroethylene in a 20% peanut oil emulsion. The pups were treated for 7 days begiiming at 10 days of age. The doses selected did not sedate the mice. At 17 and 60 days of age behavior was tested. The tests were performed between 8 am-12 pm. Locomotion, rearing, and total activity were measured in an automated device with high and low level infrared beams. [Pg.306]

Figure 7.3 shows the two-beam photon-force measurement system using a coaxial illumination photon force measurement system. Two microparticles dispersed in a liquid are optically trapped by two focused near-infrared beams ( 1 pm spot size) of a CW Nd YAG laser under an optical microscope (1064 nm, 1.2 MWcm , lOOX oil-immersion objective, NA = 1.4). The particles are positioned sufficiently far from the surface of a glass slide in order to neglect the interaction between the particles and the substrate. Green and red beams from a green LD laser (532 nm, 21 kWcm ) and a He-Ne laser (632.8 nm, 21 kW cm ) are introduced coaxially into the microscope and slightly focused onto each microparticle as an illumination light (the irradiated area was about 3 pm in diameter). The sizes of the illumination areas for the green and red beams are almost the same as the diameter of the microparticles (see Figure 7.4). The back scattered light from the surface of each microparticle is... Figure 7.3 shows the two-beam photon-force measurement system using a coaxial illumination photon force measurement system. Two microparticles dispersed in a liquid are optically trapped by two focused near-infrared beams ( 1 pm spot size) of a CW Nd YAG laser under an optical microscope (1064 nm, 1.2 MWcm , lOOX oil-immersion objective, NA = 1.4). The particles are positioned sufficiently far from the surface of a glass slide in order to neglect the interaction between the particles and the substrate. Green and red beams from a green LD laser (532 nm, 21 kWcm ) and a He-Ne laser (632.8 nm, 21 kW cm ) are introduced coaxially into the microscope and slightly focused onto each microparticle as an illumination light (the irradiated area was about 3 pm in diameter). The sizes of the illumination areas for the green and red beams are almost the same as the diameter of the microparticles (see Figure 7.4). The back scattered light from the surface of each microparticle is...
FIG. 9 Vibrational sum frequency spectrum in the OH mode region of the neat air-water interface at different temperature for the fundamental visible and infrared beams respectively s- and p-polar-ized and the SFG beam s-polarized. (From Ref. 120, copyright American Physical Society.)... [Pg.158]

Spectra were obtained using a Digilab FTS-15E Fourier Transform Spectrophotometer. A NaCl crystal mounted in a heated cell (Model 018-5322 Foxboro/Analabs, N. Haven, Ct.) was placed in the infrared beam and the chamber allowed to purge for several minutes while the cell was brought to the desired temperature. The temperature of the cell was controlled using a DuPont 900 Differential Thermal Analyzer interfaced to the spectrometer cell. A chlorobenzene solution (ca. 10 by wt.) of the sample was then applied to the crystal using cotton tipped wood splint. [Pg.243]

Simply visualised, the infrared beam penetrates (of the order 0.3-3 pm, dependent on its wavelength) just beyond the ATR crystal-specimen boundary before it is reflected back and makes its way through the crystal to the detector. On this short path (of the evanescent wave) into the sample surface layer, light is absorbed, and the reflected beam carries characteristic spectral information of the sample. The decaying amplitude of the evanescent wave and the depth of penetration dp at which it has decreased to a proportion of 1 /e is defined by the Harrick equation (Equation (2)), where X is the wavelength of the incoming... [Pg.535]

As will be shown later, the surface coverages of CO vary with distance into the pellet during CO adsorption and desorption, as a result of intrapellet diffusion resistances. However, the infrared beam monitors the entire pellet, and thus the resulting absorption band reflects the average surface concentration of CO across the pellet s depth. Therefore, for the purpose of direct comparison between theory and experiment, the integral-averaged CO coverage in the pellet... [Pg.91]

When infrared beam incidents upon thin organic films extended over a plain metal surface (Figure 1), there usually occurs a standing wave electric field on the metal surface as a consequence of the interference between the incident and reflected beams. Since the standing wave may interact with, i. e. be absorbed by, molecules in the organic film, the reflectance of the beam from the metal surface is reduced. [Pg.157]

In the normal-incident transmission measurements of LB films deposited on transparent substrates, the electric vector of the infrared beam is parallel to the film surface (Figure 5A). Therefore, only absorption bands which have the transition moments parallel to the film surface can be detected by this method. On the other hand, in the above-mentioned RA measurements, in which the p-polarized infrared beam is incident upon the LB film prepared on Ag-evaporated substrates at a large angle of incidence, we have a strong electric field perpendicular to the film surface as shown in Figure 5B. Therefore, in this case, only absorption bands which have the transition moments perpendicular to the film surface can be detected with a large intensity enhancement. Thus, if the molecules are highly oriented in the LB films, the peak intensities of particular bands should be different between the transmission and RA spectra. [Pg.160]

Although by now a large number of electrochemical systems have been examined using both SERS and IRRAS, including some common to both techniques (2b), the conditions employed are usually sufficiently different (e.g. disparate surface state, adsorbate concentrations) so to preclude a quantitative comparison of the spectral responses. One further hindrance to such comparisons is that it usually is difficult to remove entirely the contribution to the infrared spectra from solution-phase species. Two types of approaches are commonly used in IRRAS with this objective in mind. Firstly, modulating the infrared beam between s- and p-polarization can achieve a measure of demarcation between surface and bulk-phase components since considerably greater infrared absorption will occur for the former, but not the latter, species for p- versus s-polarized light (2.81. However, a complication is that the "surface... [Pg.304]

The combination of surface enhanced Raman scattering (SERS) and infrared reflection absorption spectroscopy (IRRAS) provides an effective in-situ approach for studying the electrode-electrolyte interface. The extreme sensitivity to surface species of SERS is well known. By using polarization modulation of the infrared beam for IRRAS, the complete band shape is obtained without modulating the electrode potential. [Pg.322]


See other pages where Infrared beam is mentioned: [Pg.1948]    [Pg.3001]    [Pg.288]    [Pg.192]    [Pg.192]    [Pg.195]    [Pg.196]    [Pg.197]    [Pg.199]    [Pg.199]    [Pg.201]    [Pg.423]    [Pg.747]    [Pg.748]    [Pg.107]    [Pg.242]    [Pg.113]    [Pg.75]    [Pg.375]    [Pg.111]    [Pg.1008]    [Pg.534]    [Pg.535]    [Pg.88]    [Pg.68]    [Pg.81]    [Pg.106]    [Pg.168]    [Pg.323]   
See also in sourсe #XX -- [ Pg.104 , Pg.106 , Pg.200 ]




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