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关于颗粒活性炭过滤器中有机微量污染物吸附和降解相互作用的新观点。

New Perspectives on the Interactions between Adsorption and Degradation of Organic Micropollutants in Granular Activated Carbon Filters.

机构信息

Department of Process and Life Science Engineering. Division of Chemical Engineering, Lund University, Lund 221 00, Sweden.

School of Education and Environment, Division of Natural Sciences, Kristianstad University, Kristianstad 291 88, Sweden.

出版信息

Environ Sci Technol. 2024 Jul 2;58(26):11771-11780. doi: 10.1021/acs.est.4c00815. Epub 2024 Jun 18.

DOI:10.1021/acs.est.4c00815
PMID:38889182
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11223462/
Abstract

The removal of organic micropollutants in granular activated carbon (GAC) filters can be attributed to adsorption and biological degradation. These two processes can interact with each other or proceed independently. To illustrate the differences in their interaction, three C-labeled organic micropollutants with varying potentials for adsorption and biodegradation were selected to study their adsorption and biodegradation in columns with adsorbing (GAC) and non-adsorbing (sand) filter media. Using CO formation as a marker for biodegradation, we demonstrated that the biodegradation of poorly adsorbing -nitrosodimethylamine (NDMA) was more sensitive to changes in the empty bed contact time (EBCT) compared with that of moderately adsorbing diclofenac. Further, diclofenac that had adsorbed under anoxic conditions could be degraded when molecular oxygen became available, and substantial biodegradation (≥60%) of diclofenac could be achieved with a 15 min EBCT in the GAC filter. These findings suggest that the retention of micropollutants in GAC filters, by prolonging the micropollutant residence time through adsorption, can enable longer time periods for degradations than what the hydraulic retention time would allow for. For the biologically recalcitrant compound carbamazepine, differences in breakthrough between the C-labeled and nonradiolabeled compounds revealed a substantial retention via successive adsorption-desorption, which could pose a potential challenge in the interpretation of GAC filter performance.

摘要

颗粒活性炭 (GAC) 过滤器中有机微污染物的去除可归因于吸附和生物降解。这两个过程可以相互作用或独立进行。为了说明它们相互作用的差异,选择了三种具有不同吸附和生物降解潜力的 C 标记有机微污染物,以研究它们在具有吸附(GAC)和非吸附(砂)过滤介质的柱中的吸附和生物降解。使用 CO 形成作为生物降解的标志物,我们表明,与中度吸附的双氯芬酸相比,吸附性差的 -亚硝基二甲基胺 (NDMA) 的生物降解对空床接触时间 (EBCT) 的变化更为敏感。此外,在缺氧条件下吸附的双氯芬酸在分子氧可用时可以被降解,并且在 GAC 过滤器中 15 分钟的 EBCT 可以实现双氯芬酸的大量生物降解(≥60%)。这些发现表明,通过吸附延长微污染物的停留时间,在 GAC 过滤器中保留微污染物可以使降解时间长于水力停留时间允许的时间。对于生物难降解化合物卡马西平,C 标记和非放射性标记化合物的穿透差异揭示了通过连续吸附-解吸的大量保留,这可能在解释 GAC 过滤器性能时带来潜在挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9131/11223462/278cb4713303/es4c00815_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9131/11223462/be23cdd58f74/es4c00815_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9131/11223462/e73c472cd164/es4c00815_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9131/11223462/9a24d6b3c88c/es4c00815_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9131/11223462/278cb4713303/es4c00815_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9131/11223462/be23cdd58f74/es4c00815_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9131/11223462/e73c472cd164/es4c00815_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9131/11223462/9a24d6b3c88c/es4c00815_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9131/11223462/278cb4713303/es4c00815_0004.jpg

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