Trace analysis of volatile organic compounds in water by GC and HPLC

dc.contributor.author Ogawa, Ikue
dc.contributor.department Department of Chemistry
dc.date 2018-08-16T23:09:38.000
dc.date.accessioned 2020-07-02T06:04:47Z
dc.date.available 2020-07-02T06:04:47Z
dc.date.copyright Wed Jan 01 00:00:00 UTC 1986
dc.date.issued 1986
dc.description.abstract <p>Low-molecular weight aldehydes and ketones were concentrated by a hydrophobic zeolite, ZSM-5. The carbonyl compounds (100 ppb) were desorbed with a small volume of acetonitrile and converted to the 2,4-dinitrophenylhydrazones. The derivatized analytes were recovered by solvent extraction (pentane) followed by microdistil- lation. The 2,4-dinitrophenylhydrazones were analyzed by reversed phase HPLC on a C(,18) column at 254 nm. Good recoveries were obtained for the model compounds, except formaldehyde. The method was applied to the analysis of drinking water from Ames, IA (no aldehydes or ketones) and from Des Moines, IA (1.6 ppb butanone);Other polar low-molecular weight compounds (100-200 ppb), diethyl ether, acetates, nitriles, alcohols, aldehydes, ketones and acids were concentrated by the ZSM-5 and Silicalite. Except for methanol, formaldehyde, acetic acid, and propionic acid good recoveries were obtained for model compounds. Concentration factors of 50 to 500 were achieved. Satisfactory desorbing solvents were 1-propanol, acetone, methanol and acetonitrile. The concen- trated solution was injected into a capillary (DBWax, 0.525 mm I.D.) column. The analytes were quantitated by GC with FID;The method of distillation with gas purging (helium) concentrated a variety of classes of organic (amines, alcohols, ketones, aldehydes, esters, phenols, nitriles, chlorinated compounds and polynuclear aromatic) compounds (25 ppm to 25 ppb). The entire apparatus was heated to 85(DEGREES)C or greater. The concentrating column (Tenax) was cooled. For safety a slow heating procedure was devised. The analytes were desorbed from the concentrating column by solvent elution with methanol or acetonitrile. The concentrated solution was injected into a capillary (methyl silicone, 0.525 mm I.D.) column and the analytes were quantitated by GC with FID;Recovery of the analytes was primarily dependent on the water solubility and molecular weight of the analyte. Less sample (more;headspace) was used for the strawberry jello, instant decaffeinated coffee, and shale oil retort water; ('1)DOE Report IS-T-1265. This work was performed under Contract No. W-7405-Eng-82 with the Department of Energy.</p>
dc.format.mimetype application/pdf
dc.identifier archive/lib.dr.iastate.edu/rtd/8106/
dc.identifier.articleid 9105
dc.identifier.contextkey 6328995
dc.identifier.doi https://doi.org/10.31274/rtd-180813-11529
dc.identifier.s3bucket isulib-bepress-aws-west
dc.identifier.submissionpath rtd/8106
dc.identifier.uri https://dr.lib.iastate.edu/handle/20.500.12876/81058
dc.language.iso en
dc.source.bitstream archive/lib.dr.iastate.edu/rtd/8106/r_8627141.pdf|||Sat Jan 15 02:06:47 UTC 2022
dc.subject.disciplines Analytical Chemistry
dc.subject.keywords Chemistry
dc.subject.keywords Analytic
dc.subject.keywords Chemistry
dc.title Trace analysis of volatile organic compounds in water by GC and HPLC
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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