COMPARISON OF REAGENTS FOR OFF-LINE THERMOCHEMOLYSIS OF NATURAL ORGANIC MATTER
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dc.contributor.author | Joll C.A. | |
dc.contributor.author | Couton D. | |
dc.contributor.author | Heitz A. | |
dc.contributor.author | Kagi R.I. | |
dc.date.accessioned | 2022-10-29T05:11:52Z | |
dc.date.available | 2022-10-29T05:11:52Z | |
dc.date.issued | 2004 | |
dc.identifier | https://www.elibrary.ru/item.asp?id=5190287 | |
dc.identifier.citation | Organic Geochemistry, 2004, 35, 1, 47-59 | |
dc.identifier.issn | 0146-6380 | |
dc.identifier.uri | https://repository.geologyscience.ru/handle/123456789/39235 | |
dc.description.abstract | A range of tetramethylammonium salts with different base strengths was compared for off-line thermochemolysis of an aquatic natural organic matter sample. Tetramethylammonium acetate (TMAAc) in methanol produced a different suite of compounds to the more alkaline tetramethylammonium hydroxide (TMAH) in methanol and tetramethylammonium carbonate (TMACO3) in water. TMAAc treatment produced methyl 3-methylmercaptopropanoate, but no sulfur compounds were produced from TMAH or TMACO3. Only TMAAc in methanol produced methyl esters. A mechanism for this formation of methyl esters, involving transesterification with methoxide ion derived from the solvent, was proposed. Off-line TMAAc in methanol appears to avoid decarboxylation, provide more information than on-line TMAAc and preserve more structural information than off-line TMAH in methanol or TMACO3 in water. | |
dc.title | COMPARISON OF REAGENTS FOR OFF-LINE THERMOCHEMOLYSIS OF NATURAL ORGANIC MATTER | |
dc.type | Статья |
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