Development of analytical method for plutonium in high active liquid waste solution by high performance spectrophotometry

Jitsukata, Shu*; *; ; ; Kurosawa, A.

JNC TN8410 2001-002, 66 Pages, 2000/12

JNC-TN8410-2001-002.pdf:2.03MB

It was required from IAEA to determine a small amount of plutonium in the high active liquid waste solutions (HALW) in the tokai reprocessing plant. High performance spectrophotometer (HPSP), which could be obtained lower detection limit than conventional spectrophotometer, is studied to be applied to the inspection and verification analysis by the IAEA. [Cold Test] Neodymium, showing an absorption peak near the absorption wavelength of plutonium (VI), was used as an alternative element to plutonium, in order to review the calculation method of the peak intensity. As a result, the three-point correction method was found to be simple and effective. [Hot Test] Plutonium nitrate solution was used the fundamental test of this method. Since the method is known to be influenced by acidity, suspended sludge and coexistent elements in a sample, each dependency was examined. It was found that measurement results varied about 14% at a nitric acid concentration of 2-4 mol/L. Sludge should be removed by filtration before the measurement. The effect of coexisting elements could be eliminated adjusting the optical balance between reference and sample beam intensity. In the case of measuring a low concentration plutonium solution sample, a ratio of the peak intensity to the background intensity (S/B ratio) is relatively small. Therefore a method should be improved the S/B ratio by analyzing the obtained spectra. Accumulated average method, moving average method and Fourier transform method was tested. The results showed that a combination of the accumulated average method and the moving average method was the optimum method for the purpose. Linearity of the calibration curve was found between 0-11 mgPu/L. Synthetic sample solution, which simulated the actual constituents of the HALW with plutonium showed a good linear relation at 0-11 mgPu/L. The detection limit for plutonium concentration was 0.07 mgPu/L. When the synthetic HALW solution containing plutonium was measured, the de

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; Ishibashi, Yuzo; ; ; Takeda, Seiichiro;

PNC TN8410 98-063, 48 Pages, 1997/12

PNC-TN8410-98-063.pdf:1.74MB

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; Ouchi, Yoshifusa; ;

PNC TN8450 93-005, 14 Pages, 1993/06

PNC-TN8450-93-005.pdf:1.25MB

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Spectrophotometric determination of trace amounts of boron in high purity graphite with curcumin

; Watanabe, Kazuo

Bunseki Kagaku, 42, p.T65 - T69, 1993/00

https://doi.org/10.2116/bunsekikagaku.42.5_T65

no abstracts in English

Determination of Plutonium in Nitric Acid Solution by Spectrophotometry of Pu(VI)

; ; ; ;

JAERI-M 86-032, 10 Pages, 1986/03

JAERI-M-86-032.pdf:0.39MB

no abstracts in English

Atomic absorption spectrometric determination of the isotopic composition of lithium by an ultimate absorbance-ratio technique

Analytica Chimica Acta, 183, p.225 - 230, 1986/00

https://doi.org/10.1016/0003-2670(86)80090-3

no abstracts in English

Spectrophotometric determination of zirconium in nickel-base alloys with arsenazo III after separation by froth flotation

;

Z.Anal.Chem., 288, p.47 - 49, 1977/00

no abstracts in English

Determination of traces of uranium in sea water after separation by forth flotation

Mikrochim.Acta., 1(4), p.313 - 319, 1975/04

no abstracts in English

Determination of Traces of Uranium in Sodiumafter Vacuum Distillation of Sodium; Isotopedilution and Spectrophotometric Methods

; ; ;

Bunseki Kagaku, 20(9), p.1085 - 1091, 1971/00

https://doi.org/10.2116/bunsekikagaku.20.1085

no abstracts in English