Investigation of the supercritical fluid extraction and detection of metals in contaminated soils

dc.contributor.authorLancaster, Edwin Deanen
dc.contributor.committeechairLong, Gary L.en
dc.contributor.committeememberAnderson, Mark R.en
dc.contributor.committeememberDietrich, Andrea M.en
dc.contributor.committeememberSanzone, Georgeen
dc.contributor.committeememberTissue, Brian M.en
dc.contributor.departmentChemistryen
dc.date.accessioned2014-03-14T21:12:13Zen
dc.date.adate2008-06-06en
dc.date.available2014-03-14T21:12:13Zen
dc.date.issued1996-08-05en
dc.date.rdate2008-06-06en
dc.date.sdate2008-06-06en
dc.description.abstractIn this work the Supercritical Fluid Extraction (SFE) and detection of sorbed metals in contaminated soils is explored. Iron containing samples were spiked onto sea sand and extracted with Supercritical Fluid CO₂. On-line detection was accomplished by decompressing the SF-CO₂ and analyte into a microwave induced plasma, whereby the resulting Iron atomic emission signal was quantified. This dissertation reports the first successful coupling of SFE and Microwave Induced Plasma - Atomic Emission Detection (MIP-AED) for the on-line analysis of sorbed metal contaminants. The on-line analysis was accomplished with a novel SFE-MIP interface design. Experiments involving the on-line extraction and detection of ferrocene spiked sea sand were very promising, in that unity of extraction and detection was achieved with this nonpolar compound. Percent recovery was greatly reduced when the on-line extraction of Iron III Trifluoroacetylacetonate (FeTFA) was attempted. Off-line extraction studies were performed to establish the optimum conditions necessary to effect the SFE of the following Iron III complexes: Iron III Acetylacetonate (FeAcac) and Iron III Trifluoroacetylacetonate. The greatest recovery (55.85 0/0) was achieved with Supercritical Fluid-CO₂ under the following conditions: 60°C, 150 atm, 20 minute static extraction followed by 20 minute dynamic extraction. The extraction vessel contained 0.250 mg iron complex, 20 μL HPLC grade methanol, and 20 μL deionized water. Trapping of the analyte was achieved by decompressing the SF-CO₂ and analyte in 10 mL of HPLC grade methanol held at O°C.en
dc.description.degreePh. D.en
dc.format.extentxi, 125 leavesen
dc.format.mediumBTDen
dc.format.mimetypeapplication/pdfen
dc.identifier.otheretd-06062008-151912en
dc.identifier.sourceurlhttp://scholar.lib.vt.edu/theses/available/etd-06062008-151912/en
dc.identifier.urihttp://hdl.handle.net/10919/38040en
dc.language.isoenen
dc.publisherVirginia Techen
dc.relation.haspartLD5655.V856_1996.L363.pdfen
dc.relation.isformatofOCLC# 37177493en
dc.rightsIn Copyrighten
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/en
dc.subjectmetalsen
dc.subjectsoil analysisen
dc.subjectsupercritical fluid extractionen
dc.subjectmicrowave induced plasmaen
dc.subjecton-line determinationsen
dc.subject.lccLD5655.V856 1996.L363en
dc.titleInvestigation of the supercritical fluid extraction and detection of metals in contaminated soilsen
dc.typeDissertationen
dc.type.dcmitypeTexten
thesis.degree.disciplineChemistryen
thesis.degree.grantorVirginia Polytechnic Institute and State Universityen
thesis.degree.leveldoctoralen
thesis.degree.namePh. D.en

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