Detection, identification and control of polar iodinated disinfection byproducts in chlor(am)inated secondary wastewater effluents?
Environmental Science: Water Research & Technology Pub Date: 2018-12-06 DOI: 10.1039/C8EW00718G
Abstract
Disinfection of wastewater effluents could generate numerous toxic disinfection byproducts (DBPs) during wastewater reclamation owing to the complexity of their dissolved organic matter. Recently, iodinated disinfection byproducts (I-DBPs) have attracted increasing attention as a result of their higher toxicity than their brominated and chlorinated analogues. In this study, various new polar I-DBPs in chlor(am)inated wastewater effluents were detected with ultra-performance liquid chromatography/electrospray ionization-triple quadrupole mass spectrometry (UPLC/ESI-tqMS) by setting a precursor ion scan of m/z 126.9. Three new polar I-DBPs were identified as wastewater I-DBPs, including iodoacetic acid, chloroiodoacetic acid and 3,5-diiodo-4-hydroxybenzaldehyde. The remaining new polar I-DBPs were proposed with structures, nine of which were found to be aromatic halogenated DBPs, and six of which were proposed to be in a group because they share closely related m/z values, retention times, and fragmentation pathways. In addition, formation of these new polar I-DBPs with disinfectants and contact times was also studied. Compared with chlorination, chloramination generated more species and higher concentrations of new polar I-DBPs. Furthermore, control of the newly detected polar I-DBPs during chlorination by coagulation, resin adsorption, and combined processes was compared. Resin adsorption showed a higher precursor removal efficiency than coagulation, and thus achieved a better control of these new polar I-DBPs. Coagulation followed by resin adsorption was the most effective compared with single coagulation and single resin adsorption.
Recommended Literature
- [1] An apparatus for testing water by measurement of its electrical conductivity Analyst, 1912,37, 538-543 10.1039/AN9123700538
- [2] Alt-proteins: A promising future 10.1002/fsat.3701_10.x
- [3] An autonomous self-optimizing flow machine for the synthesis of pyridine–oxazoline (PyOX) ligands? Eric Wimmer,Daniel Cortés-Borda,Solène Brochard,Elvina Barré,Charlotte Truchet,Fran?ois-Xavier FelpinReact. Chem. Eng., 2019,4, 1608-1615 10.1039/C9RE00096H
- [4] Acetyl group orientation modulates the electronic ground-state asymmetry of the special pair in purple bacterial reaction centers P. K. Wawrzyniak,M. T. P. Beerepoot,H. J. M. de Groot,F. BudaPhys. Chem. Chem. Phys., 2011,13, 10270-10279 10.1039/C1CP20213H
- [5] An integrated chip for immunofluorescence and its application to analyze lysosomal storage disorders Jie Shen,Ying Zhou,Tu Lu,Junya Peng,Zhixiang Lin,Yuhong Pang,Li YuLab Chip, 2012,12, 317-324 10.1039/C1LC20845D
- [6] Aluminium complexes with thio-phosphorus ligands: syntheses and characterisations of [Al2(CyPS3)2(CyPHS2)2] and [Al(S2PPh2)3]? Robert P. Davies,Maria A. Giménez,Laura Patel,Andrew J. P. WhiteDalton Trans., 2008, 5705-5707 10.1039/B813427H
- [7] An aptasensor for the detection of ampicillin in milk using a personal glucose meter Xixi Li,Nanwei Zhu,Ruohan Li,Qinpu ZhangAnal. Methods, 2020,12, 3376-3381 10.1039/D0AY00256A
- [8] An assay for the enzyme N-acetyl-β-d-glucosaminidase (NAGase) based on electrochemical detection using screen-printed carbon electrodes (SPCEs) R. M. Pemberton,J. P. Hart,T. T. MottramAnalyst, 2001,126, 1866-1871 10.1039/B104874K
- [9] An atom efficient route to N-aryl and N-alkyl pyrrolines by transition metal catalysis? Supaporn Sawadjoon,Joseph S. M. SamecOrg. Biomol. Chem., 2011,9, 2548-2554 10.1039/C0OB00383B
- [10] An atomistic mechanism for the degradation of perovskite solar cells by trapped charge? Eunhak Lim,Jiyoung Heo,Seong Keun KimNanoscale, 2019,11, 11369-11378 10.1039/C9NR02193K
Journal Name:Environmental Science: Water Research & Technology
research_products
-
CAS no.: 89640-58-4