TY - JOUR
T1 - Factors affecting sonolytic degradation of sulfamethazine in water
AU - Gao, Yu Qiong
AU - Gao, Nai Yun
AU - Deng, Yang
AU - Gu, Jin Shan
AU - Gu, Yu Liang
AU - Zhang, Dong
PY - 2013/11
Y1 - 2013/11
N2 - In this study, the major factors affecting sonolytic degradation of sulfamethazine (SMT), a typical pharmaceutically active compound, in water were evaluated. The factors tested included two operational parameters (i.e. initial SMT concentration and ultrasonic power), three dissolved gases (i.e. Ar, O 2 and N2), five most frequently found anions in water (NO3-,Cl-,SO42-,HCO3-andBr-), ferrous ion (Fe 2+), and four alcohols (methanol, ethanol, isopropyl alcohol, tert-butyl alcohol). Typically, the degradation rate was increased with the increasing initial SMT concentration and power. The degradation rate was accelerated in the presence of argon or oxygen, but inhibited by nitrogen. Effects of anions on the ultrasonic treatment were species-dependent. The SMT degradation rate was slightly inhibited by NO3-,Cl-,and,SO42- but significantly improved by HCO3-andBr-. The negative effects of alcohols acted as hydroxyl radicals scavengers with the following order: tert-butyl alcohol > isopropyl alcohol > ethanol > methanol. The synergetic effect of ferrous ion was mainly due to production of additional hydroxyl radicals (·OH) through Fenton chemistry. LC/MS/MS analysis indicated that the degradation of SMT by ultrasonic irradiation is mainly ascribed to ·OH oxidation. Of interest, although the SMT could be rapidly degraded by ultrasonic irradiation, the degradation products were rarely mineralized. For example, ∼100% of 180 μM SMT was decomposed, but only 8.31% TOC was reduced, within 2 h at an irradiation frequency of 800 kHz and a power of 100 W. However, the products became much biodegradable (BOD 5/COD was increased from 0.04 to 0.45). Therefore, an aerobic biological treatment may be an appropriate post-treatment to further decompose the SMT degradation products.
AB - In this study, the major factors affecting sonolytic degradation of sulfamethazine (SMT), a typical pharmaceutically active compound, in water were evaluated. The factors tested included two operational parameters (i.e. initial SMT concentration and ultrasonic power), three dissolved gases (i.e. Ar, O 2 and N2), five most frequently found anions in water (NO3-,Cl-,SO42-,HCO3-andBr-), ferrous ion (Fe 2+), and four alcohols (methanol, ethanol, isopropyl alcohol, tert-butyl alcohol). Typically, the degradation rate was increased with the increasing initial SMT concentration and power. The degradation rate was accelerated in the presence of argon or oxygen, but inhibited by nitrogen. Effects of anions on the ultrasonic treatment were species-dependent. The SMT degradation rate was slightly inhibited by NO3-,Cl-,and,SO42- but significantly improved by HCO3-andBr-. The negative effects of alcohols acted as hydroxyl radicals scavengers with the following order: tert-butyl alcohol > isopropyl alcohol > ethanol > methanol. The synergetic effect of ferrous ion was mainly due to production of additional hydroxyl radicals (·OH) through Fenton chemistry. LC/MS/MS analysis indicated that the degradation of SMT by ultrasonic irradiation is mainly ascribed to ·OH oxidation. Of interest, although the SMT could be rapidly degraded by ultrasonic irradiation, the degradation products were rarely mineralized. For example, ∼100% of 180 μM SMT was decomposed, but only 8.31% TOC was reduced, within 2 h at an irradiation frequency of 800 kHz and a power of 100 W. However, the products became much biodegradable (BOD 5/COD was increased from 0.04 to 0.45). Therefore, an aerobic biological treatment may be an appropriate post-treatment to further decompose the SMT degradation products.
KW - Sulfamethazine Sonolytic degradation Operational parameters Additives Products
UR - http://www.scopus.com/inward/record.url?scp=84879021846&partnerID=8YFLogxK
U2 - 10.1016/j.ultsonch.2013.04.007
DO - 10.1016/j.ultsonch.2013.04.007
M3 - Article
C2 - 23711347
AN - SCOPUS:84879021846
SN - 1350-4177
VL - 20
SP - 1401
EP - 1407
JO - Ultrasonics Sonochemistry
JF - Ultrasonics Sonochemistry
IS - 6
ER -