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Environmental fate of five radio-labeled coal conversion by-products evaluated in a laboratory model ecosystem

Anthracene, fluorene, carbazole, dibenzofuran, and dibenzothiophene are five typical by-products of coal conversion which are likely to be environmental pollutants. These were radiolabeled to high specific activity and purity by simple tritium exchange and evaluated for environmental fate in laborat...

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Detalles Bibliográficos
Autores principales: Lu, Po-Yung, Metcalf, Robert L., Carlson, Elaine M.
Formato: Texto
Lenguaje:English
Publicado: 1978
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1637214/
https://www.ncbi.nlm.nih.gov/pubmed/17539148
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author Lu, Po-Yung
Metcalf, Robert L.
Carlson, Elaine M.
author_facet Lu, Po-Yung
Metcalf, Robert L.
Carlson, Elaine M.
author_sort Lu, Po-Yung
collection PubMed
description Anthracene, fluorene, carbazole, dibenzofuran, and dibenzothiophene are five typical by-products of coal conversion which are likely to be environmental pollutants. These were radiolabeled to high specific activity and purity by simple tritium exchange and evaluated for environmental fate in laboratory model ecosystems. Anthracene and fluorene were biologically converted to hydroxy and keto analogs. Carbazole was N-methylated and N-acetylated. Dibenzothiophene was microsomally oxidized to the sulfoxide and sulfone. Dibenzofuran was relatively inert to biodegradation. The octanol/water partition coefficient for the parent compounds was well correlated with ecological magnification indicating the possibility of predicting environmental behavior from physicochemical parameters.
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spelling pubmed-16372142006-11-17 Environmental fate of five radio-labeled coal conversion by-products evaluated in a laboratory model ecosystem Lu, Po-Yung Metcalf, Robert L. Carlson, Elaine M. Environ Health Perspect Contributed Articles Anthracene, fluorene, carbazole, dibenzofuran, and dibenzothiophene are five typical by-products of coal conversion which are likely to be environmental pollutants. These were radiolabeled to high specific activity and purity by simple tritium exchange and evaluated for environmental fate in laboratory model ecosystems. Anthracene and fluorene were biologically converted to hydroxy and keto analogs. Carbazole was N-methylated and N-acetylated. Dibenzothiophene was microsomally oxidized to the sulfoxide and sulfone. Dibenzofuran was relatively inert to biodegradation. The octanol/water partition coefficient for the parent compounds was well correlated with ecological magnification indicating the possibility of predicting environmental behavior from physicochemical parameters. 1978-06 /pmc/articles/PMC1637214/ /pubmed/17539148 Text en
spellingShingle Contributed Articles
Lu, Po-Yung
Metcalf, Robert L.
Carlson, Elaine M.
Environmental fate of five radio-labeled coal conversion by-products evaluated in a laboratory model ecosystem
title Environmental fate of five radio-labeled coal conversion by-products evaluated in a laboratory model ecosystem
title_full Environmental fate of five radio-labeled coal conversion by-products evaluated in a laboratory model ecosystem
title_fullStr Environmental fate of five radio-labeled coal conversion by-products evaluated in a laboratory model ecosystem
title_full_unstemmed Environmental fate of five radio-labeled coal conversion by-products evaluated in a laboratory model ecosystem
title_short Environmental fate of five radio-labeled coal conversion by-products evaluated in a laboratory model ecosystem
title_sort environmental fate of five radio-labeled coal conversion by-products evaluated in a laboratory model ecosystem
topic Contributed Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1637214/
https://www.ncbi.nlm.nih.gov/pubmed/17539148
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