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- Author or Editor: S. Travnikov x
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Abstract
The possibility has been investigated of separating rare-earth fission fragment elements from106Ru and137Cs by high-temperature sublimation (950°C) of chlorides, with their subsequent gas adsorption separation in a quartz tube under a temperature gradient in a flow of the carrier-gas Ar+SOCl2. The temperature corresponding to the maxima of the element precipitation zones are: 630–660°C (144Ce), 770–780°C (0.7–6 μg140La+La), 920°C (1.5 mg Ce or La), 420–450°C (106Ru), 280–300°C (137Cs). The coefficients of element separation have been calculated. For the separation of indicator amounts of rare-earth elements and106Ru and137Cs, fractional sublimation of the chlorides of the latter at 650°C has been used. Rate constants and effective activation energies of the overall processes of chlorination-sublimation of the elements have been determined.
Abstract
The transfer and separation of the chlorides of a number of rare-earth and actinide elements and their mixtures has been investigated in the flow of gas-carrier along a quartz tube under temperature gradient. The dependence of the position (characteristic temperature) and shape of the condensation (or sorption) peak of cerium chloride in the gradient region of the tube on the amount of substance in the starting zone has been studied. Weight limits determining the behaviour of the substance as micro- or macrocomponent and its transfer by adsorption or condensation mechanism have been established. The mutual effect of elements in the La−Ce, Am−U, Np−U systems has been studied. It is shown that in the case, when the condensation peak of the macrocomponent overlaps the adsorption zone of the microcomponent, the position of the adsorption peak is shifted and the effectivity of the micro- and macrocomponent separation deteriorates in comparison with the separation of microamounts of elements. If the condensation of the macrocomponent occurs in temperature zones distant from that of the microcomponent adsorption, the position of the latter does not change and the degree of purification of the microcomponent increases.
Abstract
Trace amounts of lanthanum hexafluoroacetylacetonate and indium acetylacetonate were isolated by combination of methods, which includes synthesis of volatile elements 
-diketonates by nucleophilic ligands exchange and fractional sublimation. This method is useful for produce isotope generators.
Abstract
Separation of239Np from243Am including extraction of Np/IV/ and Am/III/ by thenoyltrifluoroacetone solution in benzene, transformation of thenoyltrifluoroacetonates into volatile hexafluoroacetylacetones in the flow of a carrier gas saturated with hexafluoroacetylacetone vapours are described.
Abstract
The temperature dependence of the vapour pressure of californium-249 hexafluoroacetylacetonate adducts with tributylphosphate /TBP/, tributylphosphineoxide /TBPO/ and dipropylsulphoxide /DPSO/ is determined. The enthalpy and entropy sublimation of the compounds are calculated.
Abstract
Volatile einsteinium hexafluoroacetylacetonate complexes have been syntehsized. Their sublimation and thermochromatographic behaviour has been studied in the presence of 
-diketone vapours. Interaction of einsteinium di-and trichloride with hexafluoracetylacetone vapours is discussed.
Abstract
A possibility to use exchange reaction of metal \-diketonates and the vapours of \-diketones for the separation of volatile \-diketonate complexes by the method of fractional sublimation has been studied. When a mixture of thenoyltrifluoroacetonates of95Zr–95Nb and Th–233Pa is treated with a carrier gas containing hexafluoroacetylacetone vapours, zirconium and thorium, unlike niobium and protactinium, form volatile hexafluoroacetyl-acetonates which sublimate quite completely at 115°C. Niobium and protactinium remain in the initial sample in the form of nonvolatile compounds.
Abstract
Volatile hexafluoroacetylacetonates of mendelevium and daughter fermium were first obtained by the interaction of hexafluoroacetylacetone with256Md radionuclide formed in the cyclotron under 
on-line
conditions as well as by the heterophase exchange of ligands. Thermochromatographic behaviour of the complexes synthesized was studied in a flow of a carrier-gas saturated with ligand vapours.
Abstract
Volatile hexafluoroacetylacetonates of hafnium, ytterbium, scandium, as well as scandium trifluoroacetylacetonate and acetylacetonate have been obtained by interaction of 
-diketone vapours with radionuclides formed in a cyclotron in on-line operation. The application of volatile -diketonates for transport and separation of the short-life isotopes of metallic elements has been shown.
