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Fate of selected pharmaceutically active compounds in the integrated fixed film activated sludge process

机译:在集成的固定膜活性污泥过程中选择的药物活性化合物的命运

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The potential for integrated fixed film activated sludge (IFAS) processes to achieve enhanced transformation of pharmaceuticals relative to conventional activated sludge (CAS) processes was assessed. Previous studies have focused on direct comparisons of parallel reactors with and without fixed film carriers and little information is available on the impacts of how varying operating parameters impact the differences in observed pharmaceutical compound (PC) transformation capabilities between CAS reactors and those equipped with both an activated sludge (AS) and fixed film carriers. The testing was carried out using bench scale sequencing batch reactors fed with authentic municipal wastewater and operated at selected combinations of temperature and solids retention time (SRT). PC transformation efficiencies were assessed in a 22 factorial design that employed the IFAS and CAS processes, operated in parallel under identical process conditions. Nitrification rate testing that was conducted to obtain insight into the biomass activity demonstrated that IFAS consistently had improved nitrification kinetics despite lower mixed liquor volatile suspended solids levels thereby demonstrating the contribution of the biofilm to nitrification. Increased transformation of atenolol (ATEN; ranging from 10-60%) and trimethoprim (TRIM; ranging from 30-50%) in the IFAS equipped reactors relative to their respective activated sludge (AS) controls was observed under all experimental conditions. Negligible transformation of carbamazepine was observed in both reactors under all conditions investigated. More than 99% of acetaminophen was transformed in both configurations under all conditions. There was no correspondence between nitrification activity and TRIM removal in the control AS while conditions that stimulated nitrification in the control AS also resulted in enhanced removal of ATEN. The results of this study indicate that the integration of biofilms in AS processes enhances transformation of some PCs.
机译:对于集成的固定膜的活性污泥(IFAS)过程的潜在达到强化相对于传统的活性污泥药物的转化(CAS)方法进行了评估。先前的研究已经集中在使用和不使用固定膜载体和小信息并联反应器的直接比较是可以用的是如何变化的操作参数影响所观察到的药物化合物(PC)CAS反应器之间转换的能力和那些配备有一个差的影响活性污泥(AS)和固定膜的载体。测试进行了使用与可信市政污水送入实验室规模序批式反应器中,并在温度和固体停留时间(SRT)选择的组合进行操作。 PC转化效率在22因子设计所采用的IFAS和CAS过程进行了评估,在操作过程中相同的条件下平行。硝化率测试这是进行以获得洞察表明,IFAS始终有尽管下混合液挥发性悬浮固体水平从而表明生物膜硝化的贡献提高硝化动力学生物质的活性。阿替洛尔的增加的转化(ATEN;范围从10-60%)和甲氧苄啶(TRIM;范围从30-50%)在配备IFAS相对于它们各自的活性污泥反应器(AS)的对照中所有实验条件下观察。在所有被调查的条件下,两个反应器中观察卡马西平可以忽略不计的转变。对乙酰氨基酚的99%以上在所有条件下都配置转化。有没有在控制硝化作用和TRIM去除之间没有对应关系,而在控制刺激硝化条件也得到了增强的ATEN的去除。这项研究的结果表明,在AS生物膜一体化处理一些个人电脑的促进转化。

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