Published 2018 | Version v1
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Quantification of Iodine-129 in radioactive waste

Description

Separation methods are required to quantify I-129, produced by U-235 and Pu-239 spontaneous fission in nuclear reactors, in radioactive waste, in order to purify and quantify it due to I-129 is a weak beta / gamma emitter difficult to quantify by gamma spectrometry, if other gamma or X emitting radionuclides are present. Therefore, the objective of this work was to develop an iodine separation methodology based on its precipitation as silver iodide (Ag129I) on an inert support. Four inert matrices were studied: Kieselgurth (SiO2), alumina (Al2O3), titanium oxide (TiO2) and Amberlite® XAD4 resin, which were impregnated with silver nitrate (AgNO3) by two methods: dynamic and static, in order to determine the retention efficiency of Ag129I on these supports. The retention of iodine on the supports was determined at three different ph s (2, 6 and 12), using as radiotracer: I-131, also a fission product of U-235, with 8 days of half-life, beta-gamma emitter easily detectable by gamma spectrometry, and that has the same chemical properties as I-129. The retention of I-131 was also determined in the presence of radioisotopes such as 99mTc, Cs-137 and Co-58. According to the Ag-I Pourbaix diagram, iodine precipitation as Ag131I is favored at ph less than 10. The highest retention efficiencies of I-131 were obtained in Amberlite XAD4 (96%) impregnated with 1 x 10-3 M AgNO3, applying the dynamic method in aqueous solutions at ph 6. Co-58 and Cs-137, also fission products, are not retained in any of the inert matrices treated studied in this work. The inert matrices and treated with AgNO3 were characterized by: X-ray diffraction, Scanning electron microscopy (Sem), Raman and Infrared spectrometry, in order to determine the structural change of the matrix when AgNO3 is impregnated. The highest percentage of silver nitrate impregnated over the MIT was obtained in the Amberlite® XAD4 with 5.9%, according to the elemental analyzes of the MIT performed by Sem. The presence of silver nitrate on the inert matrices cause's changes in the crystalline structures of the inert matrices treated, particularly when the dynamic method of impregnation is used; The highest retention of I-131 was presented in the matrix of Amberlite® XAD4 obtaining 96%. (author)

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Additional details

Additional titles

Original title (Spanish)
Cuantificacion de yodo-129 en desechos radiactivos

Publishing Information

Imprint Pagination
157 p.
Report number
INIS-MX--3522

INIS

Country of Publication
Mexico
Country of Input or Organization
Mexico
INIS RN
53064713
Subject category
S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
Resource subtype / Literary indicator
Thesis
Descriptors DEI
ALUMINIUM OXIDES; AQUEOUS SOLUTIONS; CESIUM 137; COBALT 58; FISSION PRODUCTS; GAMMA SPECTROSCOPY; IODINE; IODINE 129; IODINE 131; MATRICES; ORGANIC ION EXCHANGERS; PLUTONIUM 239; RADIOACTIVE WASTES; SCANNING ELECTRON MICROSCOPY; SILVER IODIDES; SILVER NITRATES; TECHNETIUM 99; TITANIUM OXIDES; URANIUM 235; X-RAY DIFFRACTION
Descriptors DEC
ACTINIDE NUCLEI; ALPHA DECAY RADIOISOTOPES; ALUMINIUM COMPOUNDS; BETA DECAY RADIOISOTOPES; BETA-MINUS DECAY RADIOISOTOPES; BETA-PLUS DECAY RADIOISOTOPES; CESIUM ISOTOPES; CHALCOGENIDES; COBALT ISOTOPES; COHERENT SCATTERING; DAYS LIVING RADIOISOTOPES; DIFFRACTION; DISPERSIONS; ELECTRON CAPTURE RADIOISOTOPES; ELECTRON MICROSCOPY; ELEMENTS; EVEN-ODD NUCLEI; HALIDES; HALOGEN COMPOUNDS; HALOGENS; HEAVY NUCLEI; HOMOGENEOUS MIXTURES; HOURS LIVING RADIOISOTOPES; INTERMEDIATE MASS NUCLEI; INTERNAL CONVERSION RADIOISOTOPES; IODIDES; IODINE COMPOUNDS; IODINE ISOTOPES; ION EXCHANGE MATERIALS; ISOMERIC TRANSITION ISOTOPES; ISOTOPES; MATERIALS; MICROSCOPY; MINUTES LIVING RADIOISOTOPES; MIXTURES; NITRATES; NITROGEN COMPOUNDS; NONMETALS; NUCLEI; ODD-EVEN NUCLEI; ODD-ODD NUCLEI; OXIDES; OXYGEN COMPOUNDS; PLUTONIUM ISOTOPES; RADIOACTIVE MATERIALS; RADIOISOTOPES; SCATTERING; SILVER COMPOUNDS; SILVER HALIDES; SOLUTIONS; SPECTROSCOPY; SPONTANEOUS FISSION RADIOISOTOPES; TECHNETIUM ISOTOPES; TITANIUM COMPOUNDS; TRANSITION ELEMENT COMPOUNDS; URANIUM ISOTOPES; WASTES; YEARS LIVING RADIOISOTOPES