Separation of technetium from nuclear waste stream simulants. Final report

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The authors evaluated several calorimetric assays for ReO{sub 4}{sup {minus}}, and discovered that all were flawed. They evaluated atomic absorption spectroscopy as a technique to determine sub-millimolar concentrations of ReO{sub 4}{sup {minus}}, and discovered that it is not sensitive enough for their use. However, they discovered that ICP-AES can be used to determine concentrations of ReO{sub 4}{sup {minus}} down to 0.25 ppm. They next determined that ReO{sub 4}{sup {minus}} can be quickly extracted (10 minutes or less) from aqueous HNO{sub 3} using the commercial extractant Aliquat-336 nitrate diluted with 1,3-diisopropylbenzene. Higher concentrations of extractant led to higher values of K{sub ... continued below

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66 p.

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Strauss, S.H. September 30, 1994.

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  • Strauss, S.H. Colorado State Univ., Fort Collins, CO (United States). Dept. of Chemistry

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Description

The authors evaluated several calorimetric assays for ReO{sub 4}{sup {minus}}, and discovered that all were flawed. They evaluated atomic absorption spectroscopy as a technique to determine sub-millimolar concentrations of ReO{sub 4}{sup {minus}}, and discovered that it is not sensitive enough for their use. However, they discovered that ICP-AES can be used to determine concentrations of ReO{sub 4}{sup {minus}} down to 0.25 ppm. They next determined that ReO{sub 4}{sup {minus}} can be quickly extracted (10 minutes or less) from aqueous HNO{sub 3} using the commercial extractant Aliquat-336 nitrate diluted with 1,3-diisopropylbenzene. Higher concentrations of extractant led to higher values of K{sub d} (the distribution ratio). K{sub d} was lower as the nitrate concentration of the medium increased, and was also lowered by increasing the acidity at constant nitrate ion concentration. The authors performed parallel studies with TcO{sub 4}{sup {minus}}, determining that K{sub d}(ReO{sub 4}{sup {minus}}) and K{sub d}(TcO{sub 4}{sup {minus}}) track similarly as the conditions are changed. An effort was made to prepare substituted pyridium nitrate salts that are soluble in organic solvents to be used as alternate extractants. However, in all cases but one, the salts were also soluble to some extent in the aqueous phase, significantly limiting their usefulness as extractants for these purposes. Many of the new extractant salts would partition between the organic solvent and water so that 10% of the extractant salt was in the aqueous phase. Only 1-methyl-3,5-didodecylpyridium nitrate did not show any measurable solubility in water. However, this compound was not as good an extractant as Aliquat-336. A considerable effort was also made to find suitable alternative solvents to 1,3-diisopropylbenzene. Several ketone solvents with flash points above 60 C were tested, and two of these, 2-nonanone and 3-nonanone, were superior to 1,3-diisopropylbenzene as a diluent.

Physical Description

66 p.

Notes

INIS; OSTI as DE95007645

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  • Other Information: PBD: 30 Sep 1994

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  • Other: DE95007645
  • Report No.: LA-SUB--95-30
  • Grant Number: W-7405-ENG-36
  • DOI: 10.2172/28229 | External Link
  • Office of Scientific & Technical Information Report Number: 28229
  • Archival Resource Key: ark:/67531/metadc668274

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Office of Scientific & Technical Information Technical Reports

Reports, articles and other documents harvested from the Office of Scientific and Technical Information.

Office of Scientific and Technical Information (OSTI) is the Department of Energy (DOE) office that collects, preserves, and disseminates DOE-sponsored research and development (R&D) results that are the outcomes of R&D projects or other funded activities at DOE labs and facilities nationwide and grantees at universities and other institutions.

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Creation Date

  • September 30, 1994

Added to The UNT Digital Library

  • June 29, 2015, 9:42 p.m.

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  • July 28, 2016, 7:25 p.m.

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Strauss, S.H. Separation of technetium from nuclear waste stream simulants. Final report, report, September 30, 1994; New Mexico. (digital.library.unt.edu/ark:/67531/metadc668274/: accessed December 12, 2017), University of North Texas Libraries, Digital Library, digital.library.unt.edu; crediting UNT Libraries Government Documents Department.