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Abiotic degradation of 2,4-D (dichlorophenoxyacetic acid) on synthetic birnessite: a calorespirometric method

✍ Scribed by Marcos A Cheney; Garrison Sposito; Angus E McGrath; Richard S Criddle


Book ID
103967348
Publisher
Elsevier Science
Year
1996
Tongue
English
Weight
730 KB
Volume
107
Category
Article
ISSN
0927-7757

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✦ Synopsis


Abiotic transformation of organic pollutants in soil environments can contribute significantly to remediation. As a model for the examination of abiotic remediation, the birnessite-catalyzed degradation of 2,4-D (dichlorophenoxyacetic acid) and ethyl ether was monitored by calorespirometric methods, and the products were examined by calorespirometry, chromatography and electron spin resonance (ESR) spectral analysis. Birnessite is a common componenl of man~ soils. Birnessite (modeled as the oxide mineral 6-MnO2) is an efficient solid-state catalyst of the breakdown of organic pollutants. Our results show that 2,4-D and ethyl ether adsorbed on the surface of birnessite are rapidly oxidized. Both compounds produce CO2 as a major product, but by somewhat different mechanisms. Analysis of the reaction products by high-performance liquid chromatography shows no accumulation of intermediates. Following reaction with 2,4-D, but not with ethyl ether, ESR analysis detected Mn 2+ extractable into methanol. These experiments show (a} that birnessite catalyzes the breakdown of organochlorine herbicides, such as 2,4-D and organic solvents, such as ethyl ether; (b) that CO2 is a major product of degradation for both compounds: (c) that the reaction proceeds via the birnessite-catalyzed oxidation of hydrocarbon structures, but the 2,4-D-assisted dissolution of birnessite to produce Mn 2+ is also involved in the degradation of organic solvents; and (d) that solid-state analysis by calorespirometD allows simple, rapid determinations of the reaction kinetics of pollutant breakdown.


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## Abstract The degradation of 2,4‐dichlorophenoxyacetic acid (2,4‐D) in water by the combination process of UV‐irradiation, humic acids and activated sludge treatment has been studied. The photoreaction rate of all irradiated samples was lowest for the sample irradiated at 308 nm (the XeCl excilam