BIOMINERALIZATION OF ATRAZINE OZONATION PRODUCTS - APPLICATION TO THE DEVELOPMENT OF A PESTICIDE WASTE-DISPOSAL SYSTEM

被引:18
作者
LEESON, A [1 ]
HAPEMAN, CJ [1 ]
SHELTON, DR [1 ]
机构
[1] USDA ARS, BELTSVILLE AGR RES CTR, PESTICIDE DEGRADAT LAB, BELTSVILLE, MD 20705 USA
关键词
D O I
10.1021/jf00030a030
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Development of remediation techniques for unusable pesticide wastes has led to a binary scheme involving ozonation followed by biomineralization of the resultant oxidized pesticides. Preliminary field tests of this technique indicated that the s-triazines were somewhat, more recalcitrant than the other pesticides present. Further experiments identified the final ozonation products of atrazine, the most widely used s-triazine, as 4-acetamido-6-amino-2-chloro-s-triazine (CDAT) and chlorodiamino-s-triazine (CAAT). These compounds can be utilized by microorganisms only as nitrogen sources; however, 1 % concentrations of ammonia fertilizers are not uncommon in pesticide waste. Therefore, the organism should prefer an organic nitrogen source and tolerate high ammonia concentrations. A Klebsiella terragena (strain DRS-I) was observed to degrade CAAT in the presence of high ammonia concentrations (0.8 M) with the addition of a carbon source (corn syrup), in contrast to a known s-triazine-degrading organism which could not. Nearly complete mineralization of CAAT to CO2 by DRS-1 was demonstrated using CAAT-U-ring-C-14. Bench-scale reactors indicated that continuous-flow or fixed-film reactors would support growth of DRS-1 cultures and CAAT degradation.
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页码:983 / 987
页数:5
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