Journal of the Spectroscopical Society of Japan
Online ISSN : 1884-6785
Print ISSN : 0038-7002
ISSN-L : 0038-7002
Volume 18, Issue 4
Displaying 1-4 of 4 articles from this issue
  • Wataru SUËTAKA
    1969 Volume 18 Issue 4 Pages 187-193
    Published: September 30, 1969
    Released on J-STAGE: February 23, 2011
    JOURNAL FREE ACCESS
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  • Naobumi OI
    1969 Volume 18 Issue 4 Pages 194-201
    Published: September 30, 1969
    Released on J-STAGE: June 28, 2010
    JOURNAL FREE ACCESS
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  • 13% Mn Steel, 18% Mn-5% Cr Steel
    Shizuya MAEKAWA, Takanori SUZUKI, Hiroshi MORINAGA
    1969 Volume 18 Issue 4 Pages 202-209
    Published: September 30, 1969
    Released on J-STAGE: June 28, 2010
    JOURNAL FREE ACCESS
    In order to raise the efficiency of analytical works for a high alloy steel (13% Mn steel, 18% Mn-5% Cr steel) by means of a quantorecorder, a study of quantitative analysis was made for samples obtained from molten steel in the smelting furnace, and samples from final products.The results obtained are summarized as follows:
    (1) Cr 2677.16A line is affected by Mn 2677.24A or 2676.74A line and Si 2516.12A line is affected by Mn 2516.73A line in the case of oscillatory low voltage spark, and, therefore, some correction should be made.
    (2) Analytical results obtained by the present method was satisfactory for samples in the steel-smelting process.For pit samples and samples from products, however, conventional chemical analysis should be employed.
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  • I.Apparatus and Direct Determination of Rare Earths in Lanthanum Oxide
    Tokunosuke NAKAJIMA, Hiroshi KAWAGUCHI, Kyoichiro TAKASHIMA, Yoshihiko ...
    1969 Volume 18 Issue 4 Pages 210-217
    Published: September 30, 1969
    Released on J-STAGE: February 23, 2011
    JOURNAL FREE ACCESS
    A rapid, quantitative analytical technique for the analysis of rare earth impurities is described.The method, X-ray excited optical fluorescence, uses high-energy X-rays to excite the rare earth impu-rities in appropriate matrices.The excited rare earth impurities fluorescence with simple line emission spectra which can be used for quantitative measurements.
    The experimental equipment employed is similar to that described by Linares et al. and also Sasaki.In the present study the X-ray source is a Machlett OEG-60 tungsten-target X-ray tube driven by a ARL power supply.A sample chamber is shown in Fig.2.The fluorescent radiation is made monochromatic by a Hitachi Perkin-Elmer Model 139 scanning spectrophotometer equipped with a 1440 lines/mm grating blazed at 2000Å, and detected with an photomuitiplier (HAMAMATSU TV Co., Ltd.R106) having S-19 response, and a fused silica-envelope.An amplifier equipped in the spectrophoto-meter and a chart recorder (TOA Electronics Ltd., EPR-2T) complete the system.
    Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er and Tm have been determined by this method with detection limits ranging from 0.2 ppm to 20 ppm in La2O3.
    Appreciable amounts of Pr, exceeding 500 ppm in some cases was found in commercial La2O3, which had been used as the raw material for optical glass.
    Spectrum patterns obtained for each rare earth element in La2O3 are also presented.The detection limits in other oxide systems are surveyed and discussed.
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