Intermediates of Hydrogen Peroxide-Assisted Photooxidation of Salicylic Acid: Their Degradation Rates and Ecotoxicological Assessment
International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(2), P. 697 - 697
Published: Jan. 15, 2025
Accelerated
photooxidation
of
salicylic
acid
(SA)
was
performed
using
UV
radiation
and
hydrogen
peroxide.
HPLC-MS
analysis
showed
that
the
primary
intermediates
are
2,5-dihydroxybenzoic
acid,
2,3-dihydroxybenzoic
pyrocatechol,
phenol.
Deeper
oxidation
leads
to
low
molecular
weight
aliphatic
acids,
such
as
maleic,
fumaric,
glyoxylic.
The
main
carried
out
in
same
conditions.
degradation
SA
its
follows
first-order
reaction
kinetics.
In
case
irradiation
alone,
photodegradation
is
slightly
faster
(reaction
rate
constant
0.007
min−1)
compared
(0.0052
min−1).
Other
products
degrade
more
slowly
than
SA.
Hydrogen
peroxide,
concentrations
1.8–8.8
mM,
accelerates
intermediate
products.
An
ecotoxicological
evaluation
EPI
SuiteTM
software.
overall
persistence
(POV)
long-range
transport
potential
(LRTP)
all
transformation
were
assessed
OECD
POV
LRTP
screening
tool.
Salicylic
have
toxicity.
Due
their
high
solubility,
these
contaminants
can
travel
considerable
distances
aquatic
environment.
phenol
values
156–190
km.
shorter
(less
100
km).
Language: Английский
Synthesis and Characterization of a Novel Sol–Gel-Derived Ni-Doped TiO2 Photocatalyst for Rapid Visible Light-Driven Mineralization of Paracetamol
Nanomaterials,
Journal Year:
2025,
Volume and Issue:
15(7), P. 530 - 530
Published: March 31, 2025
The
increasing
presence
of
pharmaceutical
contaminants,
such
as
paracetamol,
in
water
sources
necessitates
the
development
efficient
and
sustainable
treatment
technologies.
This
study
investigates
photocatalytic
degradation
mineralization
paracetamol
under
visible
light
using
nickel-doped
titanium
dioxide
(Ni–TiO2)
catalysts
synthesized
via
sol-gel
method.
were
characterized
through
Raman
spectroscopy,
UV–Vis
diffuse
reflectance
spectroscopy
(UV–Vis
DRS),
surface
area
measurements.
Ni
doping
enhanced
absorption
TiO2,
reducing
its
band
gap
from
3.11
eV
(undoped)
to
2.49
at
0.20
wt.%
loading,
while
analysis
confirmed
incorporation
with
anatase
predominant
phase.
Ni(0.1%)-TiO2
catalyst
exhibited
highest
activity,
achieving
88%
total
organic
carbon
(TOC)
removal
(5
ppm)
after
180
min
optimal
conditions
(catalyst
dosage,
3
g
L−1).
Stability
tests
demonstrated
84%
retained
efficiency
over
five
cycles,
a
kinetic
rate
constant
0.010
min−1.
Hydroxyl
radicals
identified
main
reactive
species.
maintained
high
performance
tap
water,
78.8%
TOC
removal.
These
findings
highlight
potential
cost-effective,
light-active
photocatalyst
for
pollutants,
promising
scalability
industrial
applications.
Language: Английский