Laser calibration

The calibration procedure is sufficiently accurate for Doppler velocities in the regime 0 to 10 mm s beyond this range, laser calibration is more suitable. Calibration with ot-iron, as described, can also be used for Mossbauer measurements with other isotopes, e.g., Ni, Au, and Ir, for which suitable standard absorbers are not available (provided that the Doppler velocity range of interest is not significantly greater than 10 mm s ). This, of course, requires that the spectrometer is temporarily equipped with a Co source and an a-iron absorber. 

Lohle, S., Battaglia, J.-L., Batsale, J.-C., Enouf, O., Dubard, J., and Filtz, J.-R. (2007) Characterization of a heat flux sensor using short pulse laser calibration. Rev. Sci. Instrum., 78, 053501. 

Fig. IX.H.5 Schematic experimental layout for UV laser calibration of distance vs. time relationship of the drift chamber. The lens focused the light into a"pencil" with a diameter of < 1mm along the active region of the detector.

A Q-switched, frequency-quadrupled Nd—YAG laser (X, = 266 nm) and its accompanying optical components produce and focus the laser pulse onto the sample surface. The typical laser spot size in this instrument is approximately 2 pm. A He-Ne pilot laser, coaxial with the UV laser, enables the desired area to be located. A calibrated photodiode for the measurement of laser energy levels is also present... 

Calibration curves must be made using a series of standards to relate emission intensities to the concentration of each element of interest. Because ICP-OES is relatively insensitive to matrix effects, pure solutions containing the element of interest often are used for calibration. For thin films the amount of sample ablated by spark discharges or laser sources is often a strong function of the sample s composition. Therefore, either standards with a composition similar to the sample s must be used or an internal standard (a known concentration of one element) is needed. 

Since the calibration factors for these techniques are known and relatively stable (depending on constant optical and geometrical parameters), the calibration process for laser-based measurements is simple or can be ignored. 

In addition to polymer standards, a number of broad distribution, water-soluble polymers can be characterized on TSK-PW columns using universal calibration. These include both fully and partially hydrolyzed PVA, PAAM, PEE, and dextran. PVA, the world s largest-volume, synthetic, water-soluble polymer, was first successfully separated on TSK-PW columns by Hashimota et al. (10). In the 1980s, the use of low-angle, laser light-scattering detection... 

Fig. 31 Evolution of the Raman spectra of a high-pressure and photo-induced sample of Se while decreasing the pressure at ca. 300 K [109]. The spectrum at 3.9 GPa shows the onset of the transformation S6 p-S. The asterisks indicate the Raman signals typical for p-S whereas the peaks of two stretching vibrations of p-S coincide with those of Se at about 458 cm and 471 cm (not indicated by asterisks). The Raman spectrum of the sample recovered at ambient pressure (0 GPa) is evidently a superposition of the spectra of a-Sg and polymeric sulfur, Sj, arrows indicate plasma lines of the Ar ion laser at 515 nm, which have been used for calibration). For Raman spectra under increasing pressure, see Fig. 23 in [1] and references cited therein...

Laboratory work involved making calibration curves which show the response of the system for various concentrations of pollutant, e.g., phenol. Typically, remote laser-induced fluorescence measurements from both the laboratory apparatus and the mobile unit are made on... 

The LIF technique is extremely versatile. The determination of absolute intermediate species concentrations, however, needs either an independent calibration or knowledge of the fluorescence quantum yield, i.e., the ratio of radiative events (detectable fluorescence light) over the sum of all decay processes from the excited quantum state—including predissociation, col-lisional quenching, and energy transfer. This fraction may be quite small (some tenths of a percent, e.g., for the detection of the OH radical in a flame at ambient pressure) and will depend on the local flame composition, pressure, and temperature as well as on the excited electronic state and ro-vibronic level. Short-pulse techniques with picosecond lasers enable direct determination of the quantum yield [14] and permit study of the relevant energy transfer processes [17-20]. 

Dreyer, C.B., Spuler, S.M., and Linne, M., Calibration of laser induced fluorescence of the OH radical by cavity ringdown spectroscopy in premixed atmospheric pressure flames. Combust. Sci. Tech., 171,163, 2001. 

At the moment, one recommends to determine the molecular characteristics of pectins using SEC chromatography equipped with a differential refractometer, a multiangle laser light scattering detector and a viscometer as previously described [25]. This technique needs no calibration with the usual molecular weight standards such dextrans and pullulans... 

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