Department of Chemical Engineering, School of Engineering, University of Santiago de Compostela, Rua Lope Gómez de Marzoa s/n, E-15782 Santiago de Compostela, Spain.
Water Res. 2012 Oct 15;46(16):5434-44. doi: 10.1016/j.watres.2012.07.037. Epub 2012 Jul 28.
High biodegradation efficiencies of different emerging micropollutants were obtained with nitrifying activated sludge (NAS) working at high nitrogen loading rates (NLR), that boosted the development of biomass with high nitrifying activities (>1 g N-NH(4)(+)/g VSS d). Come-tabolic biodegradation seemed to be responsible for the removal of most compounds due to the action of the ammonium monooxygenase enzyme. NAS showed a different affinity for each compound, probably due to steric hindrance, activation energy limitations or the presence of specific functional groups. Increasing loading rates of micropollutants were removed at shorter hydraulic retention times, although the biodegradation efficiencies of compounds with slow/intermediate kinetics, such as fluoxetine, erythromycin, roxithromycin and trimethoprim, diminished due to kinetic and/or stoichiometric limitations. Solids retention time, always above the minimum to avoid the washout of nitrifiers, did not enhance the biodegradation of any of the selected compounds, with the exception of diclofenac. Regarding sorption, the solid-liquid distribution coefficients (K(d)) obtained in NAS were very similar to those found in conventional activated sludge by other authors. No correlation between K(d) values and any of the operational parameters was found for the selected substances.
采用高氮负荷率(NLR)运行的硝化活性污泥(NAS)可实现不同新兴微量污染物的高生物降解效率,从而促进具有高硝化活性(>1 g N-NH 4 (+)/g VSS d)的生物量的发展。共代谢生物降解似乎是由于氨单加氧酶的作用负责去除大多数化合物。NAS 对每种化合物的亲和力不同,可能是由于空间位阻、活化能限制或存在特定的官能团。尽管对于具有缓慢/中等动力学的化合物(如氟西汀、红霉素、罗红霉素和甲氧苄啶),由于动力学和/或化学计量限制,生物降解效率降低,但增加微量污染物的负荷率可在更短的水力停留时间内去除。由于动力学限制,固体停留时间始终高于避免硝化菌洗出的最小值,除了双氯芬酸外,并没有增强所选化合物中的任何一种的生物降解。关于吸附,在 NAS 中获得的固-液分配系数(Kd)与其他作者在传统活性污泥中发现的非常相似。对于所选物质,未发现 Kd 值与任何操作参数之间存在相关性。