Langwaldt J H, Männistö M K, Wichmann R, Puhakka J A
Department of Environmental Technology, Institute of Water and Environmental Engineering, Tampere University of Technology, FIN-33720 Tampere, Finland.
Appl Microbiol Biotechnol. 1998 Jun;49(6):663-8. doi: 10.1007/s002530051229.
Air-lift percolator experiments simulated in situ subsurface degradation of 2,4,6-trichlorophenol, 2,3,4,6-tetrachlorophenol and pentachlorophenol, in mixtures and individually, by indigenous microorganisms from a chlorophenol-contaminated aquifer. Inoculation with a chlorophenol(CP)-degrading gram-positive isolate from the CP-contaminated groundwater did not significantly increase CP degradation rates. Feed concentrations of up to 55 mg CP l-1 were degraded. Stable CP degradation was maintained for over 6 months. CP degradation rates up to 54.3 mg l-1 day-1 and effluent concentrations below 40 micrograms CP l-1 were achieved. CP were mineralized as shown by CP reduction, dissolved organic carbon removal and release of inorganic chloride.
气升式渗滤器实验模拟了受氯酚污染含水层中的本地微生物对2,4,6-三氯酚、2,3,4,6-四氯酚和五氯酚混合物及单独物质的原位地下降解情况。用从受氯酚污染的地下水中分离出的一株降解氯酚(CP)的革兰氏阳性菌进行接种,并未显著提高CP的降解速率。高达55 mg CP l-1的进料浓度被降解。稳定的CP降解持续了6个多月。实现了高达54.3 mg l-1天-1的CP降解速率和低于40微克CP l-1的流出物浓度。通过CP减少、溶解有机碳去除和无机氯释放表明CP被矿化。