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Analysis of plutonium isotopes in marine samples by radiometric, ICP-MS and AMS techniques

dc.contributor.authorGastaud, J.
dc.contributor.authorLa Rosa, J.
dc.contributor.authorLiong Wee Kwong, L.
dc.contributor.authorPovinec, P.
dc.contributor.authorFifield, L. Keith
dc.contributor.authorHausladen, P.
dc.contributor.authordi Tada, M.
dc.contributor.authordos Santos, G
dc.contributor.authorLee, S. H.
dc.contributor.authorWyse, E.
dc.date.accessioned2015-12-13T23:27:05Z
dc.date.issued2001
dc.date.updated2015-12-12T09:49:00Z
dc.description.abstractIAEA reference materials (radionuclides in the marine environment) collected in areas affected by nuclear reprocessing plants and nuclear weapons tests have been analysed by semiconductor alpha-spectrometry (SAS), liquid scintillation spectrometry (LSS) and mass spectrometric techniques (high resolution ICP-MS and AMS) with the aim of developing analytical procedures and to study the geochemical behavior of plutonium in the marine environment. The Pu results obtained by SAS, ICP-MS and AMS were in reasonably good agreement (R2 = 0.99). The mean atom ratios of 240Pu/239Pu in IAEA reference materials, IAEA-134, 135 and 381 were (0.212±0.010), (0.211±0.004) and (0.242±0.004), respectively. IAEA-384 (Fangataufa Lagoon Sediment) gave a 24OPu/239Pu mean atom ratio of 0.051±0.001. The results of 241Pu obtained by ICP-MS and LSS also show reasonable agreement (R2 = 0.91). Pu isotopic signatures were useful in tracing Pu origin and in interpreting biogeochemical processes involving Pu in the marine environment.
dc.identifier.issn0236-5731
dc.identifier.urihttp://hdl.handle.net/1885/93155
dc.publisherAkademiai Kiado
dc.sourceJournal of Radioanalytical and Nuclear Chemistry
dc.subjectKeywords: plutonium; radioisotope; accelerator mass spectrometry; atom; atomic emission spectrometry; comparative study; conference paper; environmental monitoring; liquid scintillation counting; marine environment; mass spectrometry; sensitivity and specificity; s
dc.titleAnalysis of plutonium isotopes in marine samples by radiometric, ICP-MS and AMS techniques
dc.typeJournal article
local.bibliographicCitation.issue3
local.bibliographicCitation.lastpage764
local.bibliographicCitation.startpage757
local.contributor.affiliationS.H., Lee, International Atomic Energy Agency
local.contributor.affiliationGastaud, J., International Atomic Energy Agency
local.contributor.affiliationLa Rosa, J, National Institute of Standards and Technology
local.contributor.affiliationLiong Wee Kwong, L., International Atomic Energy Agency
local.contributor.affiliationPovinec, P, International Atomic Energy Agency
local.contributor.affiliationE., Wyse, International Atomic Energy Agency
local.contributor.affiliationFifield, L Keith, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationHausladen, P., College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationdi Tada, M., College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationdos Santos, G, College of Physical and Mathematical Sciences, ANU
local.contributor.authoruidFifield, L Keith, u8100341
local.contributor.authoruidHausladen, P., u9906569
local.contributor.authoruiddi Tada, M., u951022
local.contributor.authoruiddos Santos, G, t374
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.description.refereedYes
local.identifier.absfor040502 - Chemical Oceanography
local.identifier.ariespublicationMigratedxPub26495
local.identifier.citationvolume248
local.identifier.doi10.1023/A:1010609215926
local.identifier.scopusID2-s2.0-0034967427
local.type.statusPublished Version

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