4.8 Article

Roles of Bromine Radicals and Hydroxyl Radicals in the Degradation of Micropollutants by the UV/Bromine Process

期刊

ENVIRONMENTAL SCIENCE & TECHNOLOGY
卷 54, 期 10, 页码 6415-6426

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.0c00723

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资金

  1. Natural Science Foundation of China [21922612, 21677181, 51908564]
  2. Shanghai Tongji Gao Tingyao Environmental Science AMP
  3. Technology Development Foundation (STGEF)

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The inevitable occurrence of Br- in natural water affects the degradation kinetics of micropollutants in the UV/chlorine process, the radical chemistry of which, however, is largely unclear. As Br- in the UV/chlorine process first forms free bromine (HOBr/OBr-), this study investigated the radical chemistry of the UV/bromine process for the degradation of selected micropollutants resistant to bromine, i.e., ibuprofen and benzoate, to focus on the roles of radicals. The actual quantum yields of HOBr and OBr- by UV photolysis at 254 nm are 0.43 (+/- 0.025) and 0.26 (+/- 0.025) mol Einstein(-1), respectively. Br-center dot and HO center dot are generated first, and then, Br-2(center dot-) is formed, with the signal detectable at 360 nm by laser flash photolysis. Compared with Cl-center dot in the UV/chlorine system, Br-center dot exists at higher concentrations (similar to 10(-12) M) in the UV/bromine system while HO center dot exists at similar concentrations. In the UV/bromine process, reactive bromine species (RBS) dominates the degradation of ibuprofen, while HO center dot dominates the degradation of benzoate. Br-center dot and Br-2(center dot-) are reactive toward ibuprofen which second-order rate constants (k) were determined to be 2.2 X 10(9) and 5.3 X 10(7) M-1 s(-1), respectively, by laser flash photolysis. Be was the major RBS for ibuprofen degradation by the UV/bromine treatment, whereas Br-2(center dot-) increasingly contributed to ibuprofen degradation with increasing free bromine or Br- concentrations. Br-center dot could be scavenged by HCO3- and natural organic matter (NOM), and the k with NOM was determined to be 2.6 X 10(4) (mg/L)(-1) s(-1). Both Br-center dot and Br-2(center dot-) prefer to react with ibuprofen via electron transfer with activation energy barriers (Delta(double dagger)G(SET)(0)) of 1.35 and 7.78 kcal mol(-1), respectively. RBS promoted the formation of hydroxylated products. Then free bromine, rather than RBS, was responsible for the formation of brominated products, increasing the total organic bromine (TOBr) and tribromomethane yields in the UV/bromine system. This study demonstrates for the first time the roles of RBS and HO center dot in micropollutant degradation in the UV/bromine process.

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