Separation and determination of trace metal ions using organic chelating reagents

dc.contributor.advisor James S. Fritz
dc.contributor.author Palmieri, Margo
dc.contributor.department Department of Chemistry
dc.date 2018-08-16T16:03:50.000
dc.date.accessioned 2020-07-02T06:12:30Z
dc.date.available 2020-07-02T06:12:30Z
dc.date.copyright Thu Jan 01 00:00:00 UTC 1987
dc.date.issued 1987
dc.description.abstract <p>The separation and determination of trace metals using four different organic chelating agents is studied. The reagents tested were N,N-dihexylacetamide (DHA), 2,6-diacetylpyridine bis(furoylhydrazone) (H[subscript] 2dapf), 1,3-dimethyl-4-acetyl-2-pyrazolin-5-one (DMAP) and N-methylfurohydroxamic acid (NMFHA). DHA and H[subscript] 2dapf were investigated for their complex formation with uranium, and DMAP and NMFHA were used as chelating agents in high performance liquid chromatography (HPLC);Uranium(VI) is preferentially extracted from nitric acid solutions using DHA in toluene. The extraction characteristics of the uranium-DHA complex are studied. A 119,000 [mu]gL[superscript] -1 uranium solution is analyzed for twenty-six elements. The uranium is extracted with DHA, and the trace metal ions are then determined by inductively coupled plasma - mass spectrometry (ICP-MS). Uranium must be removed from the sample before analysis to prevent ionization suppression;The complexing agent H[subscript] 2dapf is synthesized and characterized. Studies of the complexation of metal ions with H[subscript] 2dapf is described. Uranium(VI) forms a stable complex with H[subscript] 2dapf, and a procedure for selectively determining trace uranium by spectrophotometry is presented;DMAP complexes of Cu(II), Fe(III), Ga(III), Th(IV), U(VI), V(V), and Zr(IV) are separated using reversed phase HPLC. The effects of varying chromatographic conditions on metal complex retention are described. Major changes in retention are due to solvent interaction with the metal-DMAP complexes. The conditions for quantitatively determining metal ions and a method for selectively determining uranium by HPLC of its DMAP chelate are presented;NMFHA complexes of Al(III), Fe(III), Hf(IV), Nb(V), Sb(III), and Zr(IV) are separated using reversed phase HPLC. In acidic eluents, the metal ions form cationic complexes with NMFHA and are separated using ion pairing techniques. The conditions for quantitatively determining the metal ions by HPLC of their metal chelates are described. NMFHA is also used to separate uranium(VI) from trace lanthanide ions by quantitatively sorbing the uranium-NMFHA complex onto a polymeric resin. ftn[superscript]1DOE Report IS-T 1319. This work was performed under contract No. W-7405-Eng-82 with the U.S. Department of Energy.</p>
dc.format.mimetype application/pdf
dc.identifier archive/lib.dr.iastate.edu/rtd/9287/
dc.identifier.articleid 10286
dc.identifier.contextkey 6355926
dc.identifier.doi https://doi.org/10.31274/rtd-180813-12173
dc.identifier.s3bucket isulib-bepress-aws-west
dc.identifier.submissionpath rtd/9287
dc.identifier.uri https://dr.lib.iastate.edu/handle/20.500.12876/82369
dc.language.iso en
dc.source.bitstream archive/lib.dr.iastate.edu/rtd/9287/r_8805122.pdf|||Sat Jan 15 02:30:46 UTC 2022
dc.subject.disciplines Analytical Chemistry
dc.subject.keywords Chemistry
dc.subject.keywords Analytic
dc.subject.keywords Chemistry
dc.title Separation and determination of trace metal ions using organic chelating reagents
dc.type dissertation
dc.type.genre dissertation
dspace.entity.type Publication
relation.isOrgUnitOfPublication 42864f6e-7a3d-4be3-8b5a-0ae3c3830a11
thesis.degree.level dissertation
thesis.degree.name Doctor of Philosophy
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