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Received January 27, 2010
Accepted June 2, 2010
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Biodegradation of monoethanolamine in aerobic and anoxic conditions

Department of Environmental Sciences & Biotechnology, Hallym University, Gangwon 200-702, Korea 1Department of Energy & Environmental Engineering, Soonchunhyang University, Chungnam 336-745, Korea
Korean Journal of Chemical Engineering, September 2010, 27(5), 1521-1526(6), 10.1007/s11814-010-0285-5
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Abstract

Monoethanolamine (MEA) is widely used in many industries and its proper treatment is important for protecting the water environment. As MEA contains an amine group, nitrogen removal by nitrification/denitrification as well as biodegradation of MEA is necessary for wastewater treatment. In this study the effects of adaptation and inhibition of MEA on biological degradation, and the removal of amine were investigated in a laboratory scale sequencing batch reactor (SBR). In addition, the denitrification characteristics of nitrate, and nitrite with MEA as the electron_x000D_ donor, were compared to the other electron donor (acetate). In the aerobic SBR, the removal efficiency of 9,000 mg/L MEA reached 92% at the hydraulic retention time (HRT) of 10.5 days. Ammonium hydrolyzed from the MEA was nitrified after 8 weeks from the start-up showing that adaptation time is needed for nitrification. Non-linear curve fitting of the specific MEA biodegradation gave the maximum specific activity (Vmax), the half saturation constant (Ks), and_x000D_ the inhibition constant (Ki) of 2.81 g/(g VSS·d), 102.1 mg/L, and 1149.6 mg/L, respectively. Batch denitrification showed that MEA is a competitive electron donor to acetate.

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