Journal
JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY
Volume 87, Issue 10, Pages 1489-1496Publisher
WILEY
DOI: 10.1002/jctb.3774
Keywords
F-substituent aromatics; toxicity; most negative atomic charges of molecule (q-); sorption; desorption
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Funding
- Innovative Research Team in Higher Educational Institutions of Zhejiang Provinece [T200912]
- Science and Technology Plan Projects of Hangzhou
- Zhejiang province [20091633F07, 20091633F11]
- Science and Technology Innovation Projects of Zhejiang Gongshang University [1260XJ151114]
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BACKGROUND: The commercial use of organofluorine compounds has dramatically increased over the past few years. However, little information has been reported on the potential toxicity of organofluorine compounds to anaerobic digestion processes. In this work, the effects of 4-fluorophenol (p-FP), 4-fluorobenzoic acid (p-FB) and 4-fluoroaniline (p-FA) on methanogenesis and biodegradability were evaluated using sucrose-fed systems. RESULTS: The anaerobic biodegradation of three test compounds was not observed in the study. Adsorption of p-FP, p-FB and p-FA to the sludge fitted the linear model well (r2 > 0.94). The partition coefficient Kd was 25 L kg-1 for p-FP, 16 L kg-1 for p-FB and 26 L kg-1 for p-FA. Both methanogensis and hydrolysis acidification were inhibited in the presence of three test compounds. The half maximal inhibitory concentrations (IC50s) of methanogenic activity were 339, 1390 and 1907 mg L-1 for p-FP, p-FB and p-FA, respectively. A significant linear correlation (R2 = 0.99, P < 0.05) was obtained between the half maximal inhibitory concentrations and the most negative atomic charges of molecules (q-) of the three F-substituent aromatics. CONCLUSIONS: Three F-substituent aromatics had specific effects on methanogensis, hydrolysis acidification and syntrophic cooperation in anaerobic systems. Copyright (c) 2012 Society of Chemical Industry
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