Temperature Effect on Spectrometer Slit Width and Photomultiplier Sensitivity

1968 ◽  
Vol 39 (7) ◽  
pp. 1039-1043 ◽  
Author(s):  
A. Ozolins ◽  
W. C. Lineberger ◽  
F. E. Niles
1951 ◽  
Vol 4 (2) ◽  
pp. 172
Author(s):  
JB Willis

Making certain assumptions as to the shape of infra-red absorption bands and the shape of the slit function of the monochromator, expressions are obtained for the dependence on spectrometer slit-width of the intensity and half-width of absorption bands. Experimental data to confirm the accuracy of these deductions are presented.


1978 ◽  
Vol 32 (5) ◽  
pp. 433-444 ◽  
Author(s):  
L. C. McGonagle ◽  
J. A. Holcombe

Various microphotometric (or densitometric) techniques for generating quantitative intensity information from photographically recorded spectral lines of time or spatially resolved sources are discussed. The impact of various parameters on the accuracy of quantitative densitometry is presented. These parameters include line widths of the calibration spectrum, source line broadening, microphotometer scan slit width and the optical density of the photographic image. Nonrandom errors associated with the use of various microphotometer slit widths for spectral lines of nonuniform half-width are presented. Spectral lines which are uniform and exhibit slit width or diffraction limited resolution can be scanned with any size microphotometer slit width as long as the calibration curve is prepared using the same scan slit width. The use of microphotometer slit widths narrower than the line width produce H and D curves with maximal γ and increased accuracy in the final intensity value. A density-to-intensity conversion accuracy with a 6% average error was determined for SA-1 plates. For sources whose line widths are larger than the spectrometer bandpass, minimal errors are generated by using a narrow line source for calibration and scanning this spectrum with a slit width less than the line width. Scanning of the broadened line of interest is accomplished using a scan slit width equal to approximately twice the spectrometer slit width. Under these conditions an average error of approximately 11% was determined experimentally for SA-1 plates.


1996 ◽  
Vol 50 (6) ◽  
pp. 708-714 ◽  
Author(s):  
Charlene A. Hayden ◽  
Michael D. Morris

Raman images of the distribution of materials in a sample prepared from 10-μm-diameter polystyrene spheres embedded in epoxy were reconstructed from sets of line-scanned images, with the use of univariate and multivariate processing of the spectral data. Multiple sets of microscopic Raman spectral line images were acquired by using line-focused illumination with a cylindrical lens, a motorized translation stage to move the sample perpendicular to the illumination line, and a holographic imaging spectrograph equipped with a 2D charge-coupled device (CCD) detector. Repeat sets of data were obtained at different spectrometer slit width settings and different magnification. The raw spectral data were processed by using both a simple univariate method (single-band integration) and a more sophisticated multivariate method [principal components analysis (PCA) with eigenvector rotation] to generate 2D Raman images representing spatial distribution of the individual polymeric constituents. The repeat data sets were compared to ascertain the effects of the sampling parameters on the PCA method. The results indicated that spectrometer slit width and magnification affect the sampling depth and spatial resolution, but have little effect on the PCA. Moreover, digital sampling (i.e., number of PCA wavelength variables) could be significantly reduced with little or no degradation of the PCA-generated images, particularly if key bands were represented.


Author(s):  
J. Bentley ◽  
E. A. Kenik ◽  
K. Siangchaew ◽  
M. Libera

Quantitative elemental mapping by inner shell core-loss energy-filtered transmission electron microscopy (TEM) with a Gatan Imaging Filter (GIF) interfaced to a Philips CM30 TEM operated with a LaB6 filament at 300 kV has been applied to interfaces in a range of materials. Typically, 15s exposures, slit width Δ = 30 eV, TEM magnifications ∼2000 to 5000×, and probe currents ≥200 nA, were used. Net core-loss maps were produced by AE−r background extrapolation from two pre-edge windows. Zero-loss I0 (Δ ≈ 5 eV) and “total” intensity IT (unfiltered, no slit) images were used to produce maps of t/λ = ln(IT/I0), where λ is the total inelastic mean free path. Core-loss images were corrected for diffraction contrast by normalization with low-loss images recorded with the same slit width, and for changes in thickness by normalization with t/λ, maps. Such corrected images have intensities proportional to the concentration in atoms per unit volume. Jump-ratio images (post-edge divided by pre-edge) were also produced. Spectrum lines across planar interfaces were recorded with TEM illumination by operating the GIF in the spectroscopy mode with an area-selecting slit oriented normal to the energy-dispersion direction. Planar interfaces were oriented normal to the area-selecting slit with a specimen rotation holder.


Author(s):  
João Felipe de Araujo Martos ◽  
Paulo Toro ◽  
Israel Rêgo ◽  
sergio nicolás pachón laitón ◽  
Bruno Coelho Lima

Author(s):  
SAMUEL BRITO ◽  
RODOLFO SOBRAL ◽  
Luiz Carlos Sacramento ◽  
Marcos Paulo de Souza Junior

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