TY - JOUR
T1 - Degradation of PAHs by high frequency ultrasound
AU - Manariotis, Ioannis D.
AU - Karapanagioti, Hrissi K.
AU - Chrysikopoulos, Constantinos V.
PY - 2011/4
Y1 - 2011/4
N2 - Polycyclic aromatic hydrocarbons (PAHs) are persistent organic compounds, which have been reported in the literature to efficiently degrade at low (e.g. 20 kHz) and moderate (e.g. 506 kHz) ultrasound frequencies. The present study focuses on degradation of naphthalene, phenanthrene, and pyrene by ultrasound at three different relatively high frequencies (i.e. 582, 862, and 1142 kHz). The experimental results indicate that for all three frequencies and power inputs ≥133 W phenanthrene degrades to concentrations lower than our experimental detection limit (<1 μg/L). Phenanthrene degrades significantly faster at 582 kHz than at 862 and 1142 kHz. For all three frequencies, the degradation rates per unit mass are similar for naphthalene and phenanthrene and lower for pyrene. Furthermore, naphthalene degradation requires less energy than phenanthrene, which requires less energy than pyrene under the same conditions. No hexane-extractable metabolites were identified in the solutions.
AB - Polycyclic aromatic hydrocarbons (PAHs) are persistent organic compounds, which have been reported in the literature to efficiently degrade at low (e.g. 20 kHz) and moderate (e.g. 506 kHz) ultrasound frequencies. The present study focuses on degradation of naphthalene, phenanthrene, and pyrene by ultrasound at three different relatively high frequencies (i.e. 582, 862, and 1142 kHz). The experimental results indicate that for all three frequencies and power inputs ≥133 W phenanthrene degrades to concentrations lower than our experimental detection limit (<1 μg/L). Phenanthrene degrades significantly faster at 582 kHz than at 862 and 1142 kHz. For all three frequencies, the degradation rates per unit mass are similar for naphthalene and phenanthrene and lower for pyrene. Furthermore, naphthalene degradation requires less energy than phenanthrene, which requires less energy than pyrene under the same conditions. No hexane-extractable metabolites were identified in the solutions.
KW - High frequency
KW - Naphthalene
KW - Phenanthrene
KW - Polycyclic aromatic hydrocarbons
KW - Pyrene
KW - Ultrasonic treatment
UR - http://www.scopus.com/inward/record.url?scp=79953163149&partnerID=8YFLogxK
U2 - 10.1016/j.watres.2011.02.009
DO - 10.1016/j.watres.2011.02.009
M3 - Article
C2 - 21414649
AN - SCOPUS:79953163149
SN - 0043-1354
VL - 45
SP - 2587
EP - 2594
JO - Water Research
JF - Water Research
IS - 8
ER -