Mercuric chloride-catalyzed hydrolysis of the new antifouling compound irgarol 1051
| Autor: | I. Aoyama, Y.L. Lau, Hideo Okamura, Dickson Liu, G. J. Pacepavicius, R. J. Maguire |
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| Rok vydání: | 1999 |
| Předmět: |
Reaction mechanism
Environmental Engineering Aqueous solution Chemistry Ecological Modeling Inorganic chemistry Pollution Chloride Biofouling Hydrolysis chemistry.chemical_compound medicine Tributyltin Organic chemistry Chelation Waste Management and Disposal Chemical decomposition Water Science and Technology Civil and Structural Engineering medicine.drug |
| Zdroj: | Water Research. 33:155-163 |
| ISSN: | 0043-1354 |
| DOI: | 10.1016/s0043-1354(98)00186-9 |
| Popis: | Irgarol 1051, 2-methylthio-4-tert-butylamino-6-cyclopropylamino-s-triazine, is a newly developed herbicidal additive for use in copper-based antifouling paints. It is intended to replace the antifouling agent tributyltin, which has been regulated internationally due to its severe impact on the aquatic ecosystem. However, there is no information in the open literature on the abiotic degradation of Irgarol, a fact that hinders the assessment of its ultimate impact on the environment. This study showed that mercuric chloride was capable of rapidly catalyzing the hydrolysis of Irgarol 1051 in distilled water and buffer solutions. The degradation appeared to follow the reaction of a catalyzed hydrolysis and was not significantly affected by the pH tested (5 to 9). All other 5 heavy metal salts tested (AgNO3, CdCl2, CuSO4, PbCl2 and ZnCl2) had practically no catalytic property on Irgarol hydrolysis, implying the involvement of a specific activity for Hg2+ in this reaction. The mechanism for the catalyzed hydrolysis may be the formation of bidentate chelation through nitrogen (No. 5) on the ring and the nitrogen on the cyclopropylamino side chain in Irgarol 1051 with the Hg2+ ion. The resulting four-member chelate complex would weaken the cyclopropyl-amino bond considerably, thus facilitating the hydrolysis reaction. Ultraviolet spectroscopy of the reaction mixtures and the identification of Irgarol hydrolysis product M1 (2-methylthio-4-tert-butylamino-6-amino-s-triazine) by GC-MS and LC-MS provided the basis for the proposed mechanism on the HgCl2-catalyzed hydrolysis of Irgarol 1051. M1 appeared to be more stable than the parent compound Irgarol 1051, thus implying its possible accumulation in the environment. One practical aspect of this work is that HgCl2 should not be used in preserving water samples in Irgarol 1051 monitoring programs. |
| Databáze: | OpenAIRE |
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