Study on Properties of TBP-HNO3 Complex Used for Direct Dissolution of Lanthanide and Actinide Oxides in Supercritical Fluid CO2

The tri-n-butyl phosphate-nitric acid (TBP-HNO3) complex prepared by contacting the pure TBP with the concentrated HNO3 can be used for direct dissolution of lanthanide and actinide oxides in the supercritical fluid carbon dioxide (SCF-CO2). Properties of the TBP-HNO3 complex have been studied. Expe...

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Published inChinese journal of chemistry Vol. 25; no. 3; pp. 319 - 322
Main Author 段五华 朱礼洋 景山 朱永(贝睿) 陈靖
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 01.03.2007
WILEY‐VCH Verlag
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ISSN1001-604X
1614-7065
DOI10.1002/cjoc.200790062

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Summary:The tri-n-butyl phosphate-nitric acid (TBP-HNO3) complex prepared by contacting the pure TBP with the concentrated HNO3 can be used for direct dissolution of lanthanide and actinide oxides in the supercritical fluid carbon dioxide (SCF-CO2). Properties of the TBP-HNO3 complex have been studied. Experimental results showed that when the initial HNO3/TBP volume ratio was varied from 1 : 7 to 5 : 1, the concentration of HNO3 in the TBP-HNO3 complex changed from 1.95 to 5.89 mol/L, the [HNO3]/[TBP] ratio of the TBP-HNO3 complex changed from 0.61 to 2.22, and the content of H20 in the TBP-HNO3 complex changed from 2.02% to 4.19%. All of the density, viscosity and surface tension of the TBP-HNO3 complex changed with the concentration of HNO3 in the complex, and were higher than those of the pure TBE The protons of HNO3 and H2O in the complex underwent rapid exchange to exhibit a singlet resonance peak in nuclear magnetic resonance spectra. When the TBP-HNO3 complex was dissolved in a low dielectric constant solvent, small droplets of HNO3 were formed that can be detected by NMR.
Bibliography:31-1547/O6
TL241.14
TBP-HNO3 complex, supercritical fluid carbon dioxide, property
the National Natural Science Foundation of China - No. 20506014
ark:/67375/WNG-SNSSC7DL-F
ArticleID:CJOC200790062
istex:1F157966752F4CAD55898D232A5A28C3810F34A2
Tel.: 0086‐010‐80194038; Fax: 0086‐010‐62771740
ISSN:1001-604X
1614-7065
DOI:10.1002/cjoc.200790062