Please use this identifier to cite or link to this item: https://apo.ansto.gov.au/dspace/handle/10238/9255
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dc.contributor.authorVance, ER-
dc.contributor.authorGregg, DJ-
dc.contributor.authorGriffiths, GJ-
dc.contributor.authorGaugliardo, PR-
dc.contributor.authorGrant, C-
dc.date.accessioned2020-03-26T04:47:02Z-
dc.date.available2020-03-26T04:47:02Z-
dc.date.issued2016-09-01-
dc.identifier.citationVance, E. R., Gregg, D. J., Griffiths, G. J., Gaugliardo, P. R., & Grant, C. (2016). Incorporation of Ba in Al and Fe pollucite. Journal of Nuclear Materials, 478, 256-260. doi:10.1016/j.jnucmat.2016.06.025en_AU
dc.identifier.govdoc9019-
dc.identifier.issn0022-3115-
dc.identifier.urihttps://doi.org/10.1016/j.jnucmat.2016.06.025en_AU
dc.identifier.urihttp://apo.ansto.gov.au/dspace/handle/10238/9255-
dc.description.abstractBa, the transmutation product of radioactive Cs, can be incorporated at levels of up to ∼0.07 formula units in Cs(1−2x)BaxAlSi2O6 aluminium pollucite formed by sol-gel methods and sintering at 1400 °C, with more Ba forming BaAl2Si2O8 phases. The effect of Ba substitution in pollucite-structured CsFeSi2O6 was also studied and no evidence of Ba substitution in the pollucite structure via cation vacancies or Fe2+ formation was obtained. The Ba entered a Fe-silicate glass structure. Charge compensation was also attempted with a Cs+ + Fe3+ ↔ Ba2+ + Ni2+ scheme but again the Ba formed a glass and NiO was evident. PCT leaching data showed CsFeSi2O6 to be very leach resistant. © 2016 Elsevier B.V.en_AU
dc.language.isoenen_AU
dc.publisherElsevier B.V.en_AU
dc.subjectBariumen_AU
dc.subjectAluminiumen_AU
dc.subjectPolluciteen_AU
dc.subjectPositron annihilation spectroscopyen_AU
dc.subjectIronen_AU
dc.subjectBariumen_AU
dc.subjectLeachingen_AU
dc.titleIncorporation of Ba in Al and Fe polluciteen_AU
dc.typeJournal Articleen_AU
dc.date.statistics2020-03-20-
Appears in Collections:Journal Articles

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