Treatment of raw sewage by sonuv (combined
sonication and UV irradiation) in 90 min was not
effective to mineralize the organic matter. A significant
reduction of COD was observed after 4 h
of sonuv treatment (62).
Ultrasonic can decompose other organic substrates
such as chlorinated hydrocarbons, pesticides, phenol,
explosives such as TNT, and esters, and transform
them into short-chain organic acids, CO2
and inorganic ions as the final products. The time
for complete degradation ranges from minutes to
hours (63).
The application of ultrasound to remove low-concentration
bisphenol A (BPA) in aqueous solution
at the frequency of 20 kHz, and evaluation of
ultrasonic intensity and ozone on BPA removal
was studied (64). BPA was degraded under US
in the presence of CCl4. Also they identified the
main intermediates resulting from BPA ultrasonic
degradation by GC-MS. They found that OH radical
induced oxidation is the major destruction
pathway during BPA sonolysis (64).
The degradation of bisphenol A (BPA) upon ultrasonic
action under different experimental conditions
and evaluation of saturating gas, BPA concentration,
ultrasonic frequency and power has
been studied (65). They found that for 118 μmol/L
BPA solution, the best performance obtained at
300 kHz, 80 W, and oxygen as saturating gas. In
these conditions, BPA readily eliminated by ultrasound
process (90 min). Identified intermediates
were: monohydroxylated bisphenol A, 4-
isopropenylphenol, quinone of monohydroxylated
bisphenol A, dihydroxylated bisphenol A, quinone
of dihydroxylated bisphenol A, monohydroxylated-
4-isopropenylphenol and 4-hydroxyacetophenone
(65)
A novel hybrid advanced oxidation technique
(sonoelectro-Fenton process) was applied for the
degradation of organic pollutants in aqueous medium
(66). They coupled ultrasound irradiation
and the in-situ electrogeneration of Fenton’s reagent.
They studied synergistic action of sonication
in the sono-EF process at low and high frequency.
It was demonstrated that destruction of
herbicides 4, 6-dinitro-o-cresol (DNOC) and 2,
4-dichlorophenoxyacetic acid (2, 4-D) is significantly
accelerated. They concluded that improvement
yielded by sonoelectro-Fenton process
is due to various contributions: (i) enhanced mass
transfer rate of reactants towards cathode, (ii) additional
generation of OH by sonolysis, and (iii)
pyrolysis of organics due to cavitation generated
by ultrasound irradiation (66).
The potential of using ultrasonic irradiation for
the removal of sodium dodecylbenzene sulfonate
(SDBS) at concentrations of 15, 30 and 100 mg/L
from aqueous solutions with power values of 45,
75 and 150 W was studied (67). Results showed
that SDBS conversion decrease with increasing
temperature and initial solute concentration and decreasing
power and frequency. Investigations using
the radical scavengers 1-butanol and KBr revealed
that SDBS degradation proceeds through
radical reactions occurring predominately at the
bubble-liquid interface and, to a lesser extent, in
the liquid bulk. In this research addition of NaCl
or H2O2 had little or even an adverse effect on
SDBS conversion (67).
In another research the effect of various operating
conditions and the presence of matrix components
on the sonochemical degradation of naphthalene,
acenaphthylene and phenanthrene in water
was studied (68). At the operating conditions in
question (initial concentrations of 150, 300 and
450 μg/l, temperatures of 20 and 40° C, applied
power of 45, 75 and 150 W and ultrasound frequencies
of 24 and 80 kHz), all PAHs were susceptible
to sonochemical treatment and, in most
cases, complete degradation could be achieved in
up to 120 min of treatment. Conversion was found
to decrease with increasing initial concentration
and temperature and decreasing power and frequency
as well as in the presence of an excess
of dissolved salts (68).
sonication and UV irradiation) in 90 min was not
effective to mineralize the organic matter. A significant
reduction of COD was observed after 4 h
of sonuv treatment (62).
Ultrasonic can decompose other organic substrates
such as chlorinated hydrocarbons, pesticides, phenol,
explosives such as TNT, and esters, and transform
them into short-chain organic acids, CO2
and inorganic ions as the final products. The time
for complete degradation ranges from minutes to
hours (63).
The application of ultrasound to remove low-concentration
bisphenol A (BPA) in aqueous solution
at the frequency of 20 kHz, and evaluation of
ultrasonic intensity and ozone on BPA removal
was studied (64). BPA was degraded under US
in the presence of CCl4. Also they identified the
main intermediates resulting from BPA ultrasonic
degradation by GC-MS. They found that OH radical
induced oxidation is the major destruction
pathway during BPA sonolysis (64).
The degradation of bisphenol A (BPA) upon ultrasonic
action under different experimental conditions
and evaluation of saturating gas, BPA concentration,
ultrasonic frequency and power has
been studied (65). They found that for 118 μmol/L
BPA solution, the best performance obtained at
300 kHz, 80 W, and oxygen as saturating gas. In
these conditions, BPA readily eliminated by ultrasound
process (90 min). Identified intermediates
were: monohydroxylated bisphenol A, 4-
isopropenylphenol, quinone of monohydroxylated
bisphenol A, dihydroxylated bisphenol A, quinone
of dihydroxylated bisphenol A, monohydroxylated-
4-isopropenylphenol and 4-hydroxyacetophenone
(65)
A novel hybrid advanced oxidation technique
(sonoelectro-Fenton process) was applied for the
degradation of organic pollutants in aqueous medium
(66). They coupled ultrasound irradiation
and the in-situ electrogeneration of Fenton’s reagent.
They studied synergistic action of sonication
in the sono-EF process at low and high frequency.
It was demonstrated that destruction of
herbicides 4, 6-dinitro-o-cresol (DNOC) and 2,
4-dichlorophenoxyacetic acid (2, 4-D) is significantly
accelerated. They concluded that improvement
yielded by sonoelectro-Fenton process
is due to various contributions: (i) enhanced mass
transfer rate of reactants towards cathode, (ii) additional
generation of OH by sonolysis, and (iii)
pyrolysis of organics due to cavitation generated
by ultrasound irradiation (66).
The potential of using ultrasonic irradiation for
the removal of sodium dodecylbenzene sulfonate
(SDBS) at concentrations of 15, 30 and 100 mg/L
from aqueous solutions with power values of 45,
75 and 150 W was studied (67). Results showed
that SDBS conversion decrease with increasing
temperature and initial solute concentration and decreasing
power and frequency. Investigations using
the radical scavengers 1-butanol and KBr revealed
that SDBS degradation proceeds through
radical reactions occurring predominately at the
bubble-liquid interface and, to a lesser extent, in
the liquid bulk. In this research addition of NaCl
or H2O2 had little or even an adverse effect on
SDBS conversion (67).
In another research the effect of various operating
conditions and the presence of matrix components
on the sonochemical degradation of naphthalene,
acenaphthylene and phenanthrene in water
was studied (68). At the operating conditions in
question (initial concentrations of 150, 300 and
450 μg/l, temperatures of 20 and 40° C, applied
power of 45, 75 and 150 W and ultrasound frequencies
of 24 and 80 kHz), all PAHs were susceptible
to sonochemical treatment and, in most
cases, complete degradation could be achieved in
up to 120 min of treatment. Conversion was found
to decrease with increasing initial concentration
and temperature and decreasing power and frequency
as well as in the presence of an excess
of dissolved salts (68).