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个人信息Personal Information
副教授
博士生导师
硕士生导师
任职 : 环境生态与工程研究生导师纵向党支部书记
性别:男
毕业院校:中科院南京土壤所
学位:博士
所在单位:环境学院
学科:环境科学
办公地点:环境楼B409
联系方式:办公电话:84707189 手机:13610848936
电子邮箱:xlqiao@dlut.edu.cn
Distinct Photolytic Mechanisms and Products for Different Dissociation Species of Ciprofloxacin
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论文类型:期刊论文
发表时间:2013-05-07
发表刊物:ENVIRONMENTAL SCIENCE & TECHNOLOGY
收录刊物:SCIE、EI、PubMed、PKU、ISTIC、Scopus
卷号:47
期号:9
页面范围:4284-4290
ISSN号:0013-936X
摘要:As many antibiotics are ionizable and may have different dissociation forms in the aquatic environment, we hypothesized that the different dissociation species have disparate photolytic pathways, products, and kinetics, and adopted ciprofloxacin (CIP) as a case to test this hypothesis. Simulated sunlight experiments and matrix calculations were performed to differentiate the photolytic reactivity for each dissociation species (H4CIP3+, H3CIP2+, H2CIP+, HCIP0, and CIP-). The results prove that the five dissociation species do have dissimilar photolytic kinetics and products. H4CIP3+ mainly undergoes stepwise cleavage of the piperazine ring, while H2CIP+ mainly undergoes defluorination. For H3CIP2+, HCIP, and CIP, the major photolytic pathway is oxidation. By density functional theory calculation, we clarified the defluorination mechanisms for the five dissociation species at the excited triplet states: All the five species can defluorinate by reaction with hydroxide ions (OH-) to form hydroxylated products, and H2CIP+ can also undergo C-F bond cleavage to produce F- and a carbon-centered radical. This study is a first attempt to differentiate the photolytic products and mechanisms for different dissociation species of ionizable compounds. The results imply that for accurate ecological risk assessment of ionizable emerging pollutants, it is necessary to investigate the environmental photochemical behavior of all dissociation species.