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Determination of rhodium by thermal neutron activation analysis using g-ray spectrometry

dc.contributor.authorSteele, Edgar L.en_US
dc.contributor.authorWayne Meinke, W.en_US
dc.date.accessioned2006-04-13T14:56:20Z
dc.date.available2006-04-13T14:56:20Z
dc.date.issued1962en_US
dc.identifier.citationSteele, Edgar L., Wayne Meinke, W. (1962)."Determination of rhodium by thermal neutron activation analysis using g-ray spectrometry." Analytica Chimica Acta 26(): 269-274. <http://hdl.handle.net/2027.42/32335>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6TF4-4502478-15H/2/cb3ee9f998d2d0cfa046401ddf3ba69een_US
dc.identifier.urihttps://hdl.handle.net/2027.42/32335
dc.description.abstractTrace amounts of rhodium have been determined by thermal neutron activation analysis using both destructive and non-destructive methods. With a neutron flux of 1012 n cm-2 sec-1 the lower limits of detection are about 0.1 [mu]g and 0.01 [mu]g, respectively. A rapid sodium-peroxide fusion followed by a pyridine extraction was used in the destructive method to separate the 4.4-mm 104mRh from its matrix. The 44-sec104Rh was used in the non-destructive method. Both radioactive isomers were measured by [gamma]-ray spectrometry with a multichannel pulse height analyzer. The average time required per non-destructive analysis was 7 min while the chemical method averaged 20 min.en_US
dc.format.extent515538 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleDetermination of rhodium by thermal neutron activation analysis using g-ray spectrometryen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, Michigan U.S.A.en_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, Michigan U.S.A.en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/32335/1/0000405.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/S0003-2670(00)88383-Xen_US
dc.identifier.sourceAnalytica Chimica Actaen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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