Title of article
Microbial atrazine mineralisation under carbon limited and denitrifying conditions
Author/Authors
Gerhard Stucki، نويسنده , , Chi W. Yu، نويسنده , , Thomas Baumgartner، نويسنده , , Juan F. Gonzalez-Valero، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 1995
Pages
6
From page
291
To page
296
Abstract
A microbial enrichment culture was able to mineralise atrazine (2-chloro-4-ethylamino-6-isopropylamino-1,3,5-triazine) supplied as sole carbon and energy source. The microorganisms were immobilised in a non-aerated fixed bed reactor with sintered glass beds as carrier matrix. Atrazine elimination was rapid, efficient and quantitative. With feed rates of up to 15.5 l d−1 of medium containing 7.5 mg l−1 atrazine, the hydraulic retention time in the 300 ml reactor decreased to below 30 min. Atrazine effluent concentrations under these conditions were in the 10–100 μg l−1-range. The mineralisation of atrazine became incomplete under oxygen deficient conditions observed with atrazine feed concentrations of 15 mg l−1. However, complete atrazine conversion was regained and the effluent levels dropped to below 10 μg l−1 when NO3−-ions (66 mg l−1) were supplemented to this medium. When [U-ring-14C]atrazine (7–15 mg l−1) was used in the feed medium and a hydraulic residence time of 3.6 h was applied, atrazine was not detectable (<0.2 μg l−1) in the effluent. The yield of 14CO2 in relation to the radioactivity applied to the system was 33% under C-limited and 44% under denitrifying conditions, respectively. Under low oxygen concentrations, only 77% of the atrazine was converted, and only 12% of the radioactivity was obtained as 14CO2, whereas a total of 61% of the radioactivity could be attributed to two water soluble metabolites, 2-hydroxy-4-ethylamino-6-isopropylamino-1,3,5-triazine and 2-chloro-4-amino-6-isopropylamino-1,3,5-triazine.
Keywords
Atrazine , Denitrifying conditions , herbicide , mineralisation
Journal title
Water Research
Serial Year
1995
Journal title
Water Research
Record number
765217
Link To Document