Filters
Results 1 - 1 of 1
Results 1 - 1 of 1.
Search took: 0.029 seconds
Cui, Changzheng; Jin, Lei; Jiang, Lei; Han, Qi; Lin, Kuangfei; Lu, Shuguang; Zhang, Dong; Cao, Guomin, E-mail: cuichangzheng@ecust.edu.cn2016
AbstractAbstract
[en] Trace levels of residual antibiotics in drinking water may threaten public health and become a serious problem in modern society. In this work, we investigated the degradation of twelve sulfonamides (SAs) at environmentally relevant trace level concentrations by three different methods: ultraviolet (UV) photolysis, peroxymonosulfate (PMS) oxidation, and UV-activated PMS (UV/PMS). Sulfaguanidine, sulfadiazine, sulfamerazine, sulfamethazine, sulfathiazole, sulfamethoxydiazine, and sulfadimethoxine were be effectively removed by direct UV photolysis and PMS oxidation. However, sulfanilamide, sulfamethizole, sulfamethoxazole, sulfisoxazole, and sulfachloropyridazine were not completely degraded, despite prolonging the UV irradiation time to 30 min or increasing the PMS concentration to 5.0 mg·L−1. UV/PMS provided more thorough elimination of SAs, as demonstrated by the complete removal of 200 ng·L−1 of all SAs within 5 min at an initial PMS concentration of 1.0 mg·L−1. UV/PMS promoted SA decomposition more efficiently than UV photolysis or PMS oxidation alone. Bicarbonate concentration and pH had a negligible effect on SA degradation by UV/PMS. However, humic acid retarded the process. Removal of 200 ng·L−1 of each SA from a sample of sand-filtered effluent from a drinking water treatment plant (DWTPs) was quickly and completely achieved by UV/PMS. Meanwhile, about 41% of the total organic carbon (TOC) was eliminated. Scavenging experiments showed that sulfate radical (SO4·−) was the predominant species involved in the degradation. It is concluded that UV/PMS is a rapid and efficient method for removing trace-level SAs from drinking water. - Highlights: • Trace-level sulfonamides were removed from drinking water. • UV, peroxymonosulfate (PMS), and UV-activated PMS were used for the removal. • Sulfonamides with five-membered heterocycles had more rapid photolysis. • Heterocyclic ring structure greatly affected photolysis and PMS oxidation. • UV/PMS could quickly and completely eliminate trace-level sulfonamides.
Primary Subject
Source
S0048-9697(16)31637-0; Available from http://dx.doi.org/10.1016/j.scitotenv.2016.07.183; Copyright (c) 2016 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; Country of input: International Atomic Energy Agency (IAEA)
Record Type
Journal Article
Journal
Country of publication
AMIDES, ANTI-INFECTIVE AGENTS, ANTIMICROBIAL AGENTS, CHEMICAL REACTIONS, DECOMPOSITION, DIMENSIONLESS NUMBERS, DRUGS, ELECTROMAGNETIC RADIATION, HETEROCYCLIC COMPOUNDS, HYDROGEN COMPOUNDS, ORGANIC ACIDS, ORGANIC COMPOUNDS, ORGANIC NITROGEN COMPOUNDS, ORGANIC SULFUR COMPOUNDS, OXYGEN COMPOUNDS, PHOTOCHEMICAL REACTIONS, RADIATIONS, REMOVAL, WATER
Reference NumberReference Number
INIS VolumeINIS Volume
INIS IssueINIS Issue