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Infrared emission

Emission infrared spectroscopy is used for thin films and opaque polymers. The sample is heated so that energy is emitted. The sample acts as the radiation source and the emitted radiation is recorded giving spectra similar to those of classical FTIR. In some cases, IR frequencies vary because of differences in the structures at different depths and interactions between surface and interior emissions. [Pg.426]

B. Dimensional Stability Boroscope Miniaturized T.V. Microscope Radiation Reflectance or Diffraction Photocell (visible) X-ray diffraction U.V. reflectance spectroscope y-Ray back-scatter Scintillation read out Infrared reflectance Radiation emission Infrared scan Profilometer... [Pg.242]

Emissivity - [INFRARED TECHNOLOGY AND RAMAN SPECTEOSCOPY - INFRARED TECHNOLOGY] (Vol 14)... [Pg.360]

When air is heated to between 2000-6000 K and passed over a PTFE surface, carbonyl difluoride is detected by its emission infrared spectrum in the PTFE/air boundary layer [2239]. COF j has also been detected in an ablating flat plate air-PTFE laminar boundary layer [820,821] generated with a subsonic free stream of air (1 atm, 3000-6000 K) produced by an arc jet CO, COj, and NO were also observed in this experiment. [Pg.595]

Once the transient species has been formed, it has to be monitored by some form of kinetic spectroscopy, typically with ultraviolet-visible absorption or emission, infrared (time-resolved infrared or TRIR) (74), or resonance Raman (time-resolved resonance Raman or TR3) (80) methods of detection. The transient is usually tracked by a probe beam at a single characteristic frequency, thereby giving direct access to the kinetic dimension. Spectra can then be built up point by point, if necessary, with an appropriate change of probe frequency for each point, although improvements in the sensitivity of multichannel detectors may be expected to lead increasingly to the replacement of the laborious point-by-point method by full two-dimensional methods of spectroscopic assay (that is, with both spectral and kinetic dimensions). [Pg.137]

Balkin (5) found the following infrared spectral changes to occur upon transition from the crystalline to the nematic and from the nematic to isotropic liquid phase under stationary conditions. (He used absorption rather than emission infrared spectroscopy.)... [Pg.81]

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]

Active thermography is a contactless NDE technique that consists in the detection of infrared emission after the transient thermal excitation of the inspected structure. [Pg.393]

The eombination in a compact system of an infrared sensor and a laser as excitation source is called a photothermal camera. The surface heating is aehieved by the absorption of the focused beam of a laser. This localisation of the heating permits a three-dimensional heat diffusion in the sample to be examined. The infrared (IR) emission of the surface in the neighbourhood of the heating spot is measured by an infrared detector. A full surface inspection is possible through a video scanning of the excitation and detection spots on the piece to test (figure 1). [Pg.393]

The research activity here presented has been carried out at the N.D.T. laboratory of l.S.P.E.S.L. (National Institute for Occupational Safety and Prevention) and it is aimed at the set up of the Stress Pattern Analysis by Measuring Thermal Emission technique [I] applied to pressure vessels. Basically, the SPATE system detects the infrared flux emitted from points resulting from the minute temperature changes in a cyclically stressed structure or component. [Pg.408]

IRE Infrared emission [110] Infrared emission from a metal surface is affected in angular distribution by adsorbed species Orientation of adsorbed molecules... [Pg.314]

IRE Infrared emission IR emission spectrum observed High resolution, long... [Pg.317]

Vibrational Spectroscopy. Infrared absorption spectra may be obtained using convention IR or FTIR instrumentation the catalyst may be present as a compressed disk, allowing transmission spectroscopy. If the surface area is high, there can be enough chemisorbed species for their spectra to be recorded. This approach is widely used to follow actual catalyzed reactions see, for example. Refs. 26 (metal oxide catalysts) and 27 (zeolitic catalysts). Diffuse reflectance infrared reflection spectroscopy (DRIFT S) may be used on films [e.g.. Ref. 28—Si02 films on Mo(llO)]. Laser Raman spectroscopy (e.g.. Refs. 29, 30) and infrared emission spectroscopy may give greater detail [31]. [Pg.689]

The first mfonnation on the HE vibrational distribution was obtained in two landmark studies by Pimentel [39] and Polanyi [24] in 1969 both studies showed extensive vibrational excitation of the HE product. Pimental found that tire F + H2 reaction could pump an infrared chemical laser, i.e. the vibrational distribution was inverted, with the HF(u = 2) population higher than that for the HF(u = 1) level. A more complete picture was obtained by Polanyi by measuring and spectrally analysing tlie spontaneous emission from vibrationally excited HE produced by the reaction. This infrared chemiluminescence experiment yielded relative populations of 0.29, 1 and 0.47 for the HF(u =1,2 and 3)... [Pg.876]

Maranowski K D, Gossard A C, Unterrainer K and Gornik E 1996 Far-infrared emission from parabolioally graded quantum wells Appl. Rhys. Lett. 69 3522-4... [Pg.1260]

Almost every modem spectroscopic approach can be used to study matter at high pressures. Early experiments include NMR [ ], ESR [ ] vibrational infrared [33] and Raman [ ] electronic absorption, reflection and emission [23, 24 and 25, 70] x-ray absorption [Tf] and scattering [72], Mossbauer [73] and gems analysis of products recovered from high-pressure photochemical reactions [74]. The literature contains too many studies to do justice to these fields by describing particular examples in detail, and only some general mles, appropriate to many situations, are given. [Pg.1961]

Optical metiiods, in both bulb and beam expermrents, have been employed to detemiine tlie relative populations of individual internal quantum states of products of chemical reactions. Most connnonly, such methods employ a transition to an excited electronic, rather than vibrational, level of tlie molecule. Molecular electronic transitions occur in the visible and ultraviolet, and detection of emission in these spectral regions can be accomplished much more sensitively than in the infrared, where vibrational transitions occur. In addition to their use in the study of collisional reaction dynamics, laser spectroscopic methods have been widely applied for the measurement of temperature and species concentrations in many different kinds of reaction media, including combustion media [31] and atmospheric chemistry [32]. [Pg.2071]

The section on Spectroscopy has been retained but with some revisions and expansion. The section includes ultraviolet-visible spectroscopy, fluorescence, infrared and Raman spectroscopy, and X-ray spectrometry. Detection limits are listed for the elements when using flame emission, flame atomic absorption, electrothermal atomic absorption, argon induction coupled plasma, and flame atomic fluorescence. Nuclear magnetic resonance embraces tables for the nuclear properties of the elements, proton chemical shifts and coupling constants, and similar material for carbon-13, boron-11, nitrogen-15, fluorine-19, silicon-19, and phosphoms-31. [Pg.1284]

Colorimetry, in which a sample absorbs visible light, is one example of a spectroscopic method of analysis. At the end of the nineteenth century, spectroscopy was limited to the absorption, emission, and scattering of visible, ultraviolet, and infrared electromagnetic radiation. During the twentieth century, spectroscopy has been extended to include other forms of electromagnetic radiation (photon spectroscopy), such as X-rays, microwaves, and radio waves, as well as energetic particles (particle spectroscopy), such as electrons and ions. ... [Pg.368]

In principle, emission spectroscopy can be applied to both atoms and molecules. Molecular infrared emission, or blackbody radiation played an important role in the early development of quantum mechanics and has been used for the analysis of hot gases generated by flames and rocket exhausts. Although the availability of FT-IR instrumentation extended the application of IR emission spectroscopy to a wider array of samples, its applications remain limited. For this reason IR emission is not considered further in this text. Molecular UV/Vis emission spectroscopy is of little importance since the thermal energies needed for excitation generally result in the sample s decomposition. [Pg.434]

The majority of infrared spectra are obtained by an absorption rather than an emission process and, as a result, the change of signal intensity 1(5) with retardation 5 appears very different from that in Figure 3.13. [Pg.57]

In the process of absorption or emission of infrared radiation involving transitions between two vibrational states the interaction is usually between the molecule and the electric, rather than the magnetic, component of the electromagnetic radiation (see Section 2.1). For this... [Pg.166]

The word laser is an acronym derived from light amplification by the stimulated emission of radiation . If the light concerned is in the microwave region then the alternative acronym maser is often used. Although the first such device to be constructed was the ammonia maser in 1954 it is the lasers made subsequently which operate in the infrared, visible or ultraviolet regions of the spectrum which have made a greater impact. [Pg.337]


See other pages where Infrared emission is mentioned: [Pg.214]    [Pg.354]    [Pg.308]    [Pg.214]    [Pg.354]    [Pg.308]    [Pg.151]    [Pg.873]    [Pg.1140]    [Pg.1233]    [Pg.1235]    [Pg.1237]    [Pg.1780]    [Pg.2060]    [Pg.2447]    [Pg.2895]    [Pg.122]    [Pg.123]    [Pg.292]    [Pg.295]    [Pg.101]    [Pg.281]    [Pg.191]    [Pg.194]   


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Emission and absorption of radiation Infrared

Fourier Transform Infrared Emission Spectroscopy (FT-IRES)

Fourier transform infrared emission

Fourier transform infrared emission measurements

Infrared emission spectra

Infrared emission spectrometry

Infrared emission spectrometry principles

Infrared emission spectroscopy applications

Infrared emission, from vibrationally excited

Infrared emission, from vibrationally excited species

Infrared emissions from dust disks

Infrared excess emission

Infrared spectroscopy emission measurements

Interstellar medium infrared emission

Near infrared excitation/emission

Near infrared excitation/emission imaging

Near-infrared emission

Near-infrared emission 3-diketone ligands

Near-infrared emission ionic liquids

Near-infrared emission lanthanide complexes

Near-infrared emission lanthanide ions

Near-infrared emission ligands

Near-infrared emission luminescence

Near-infrared emission materials

Near-infrared emission photoluminescence

Near-infrared emission photophysics

Near-infrared emission polymers

Near-infrared emission silicates

Near-infrared emission upconversion

Near-infrared emissive polymersomes

Polycyclic aromatic hydrocarbons infrared emission bands

Reduction of Infrared Emission from Combustion Products

Relative Quantification of Catalytic Activity in Combinatorial Libraries by Emissivity-Corrected Infrared Thermography

Spectroscopy infrared emission

Transient infrared emission spectroscopy

Transient infrared emission spectroscopy TIRES)

Transition metal ions infrared emissions

Unidentified infrared emission bands

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