Construction of carboxyl-functionalized hyper-cross-linked porous polymers using waste polystyrene for effective adsorption of phenolic contaminants
Chenhuan Wang,
No information about this author
Qianqian Wang,
No information about this author
Kaiyuan Si
No information about this author
et al.
Journal of Chromatography A,
Journal Year:
2025,
Volume and Issue:
unknown, P. 465925 - 465925
Published: March 1, 2025
Language: Английский
Photooxidation of Polystyrene into High‐Value Chemicals
Shaokai Jiang,
No information about this author
Yunhan Chen,
No information about this author
Yahao Huang
No information about this author
et al.
European Journal of Organic Chemistry,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 5, 2024
Abstract
Plastics
play
a
crucial
role
in
the
survival
and
advancement
of
human
civilization.
However,
increasing
challenge
plastic
pollution
presents
significant
obstacles.
Disposal
methods
such
as
incineration
landfilling
result
substantial
resource
wastage
pose
potential
environmental
hazards.
The
slow
progress
recycling
reusing
waste
plastics
hinders
their
industrial
application
effective
response
to
crises.
Photocatalysis
offers
promising
solutions
for
future
recycling,
particularly
with
recent
increase
photocatalytic
degradation
polystyrene
(PS).
This
review
provides
comprehensive
overview
latest
advancements
photooxidation
PS
into
high‐value
chemicals.
Language: Английский
Reassessing the Photochemical Upcycling of Polystyrene Using Acridinium Salts
Anne‐Lise De Abreu,
No information about this author
Daniel Taton,
No information about this author
Dario M. Bassani
No information about this author
et al.
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 13, 2024
Abstract
Polystyrene
(
PS
)
is
a
commodity
plastic
recalcitrant
to
chemical
recycling
or
upcycling
processes.
Approaches
aimed
at
deconstructing
by
photocatalytic
means
struggle
generate
high‐energy
species
capable
of
cleaving
the
robust
C−H
and
C−C
bonds
.
We
show
that
9‐mesityl‐10‐methylacridinium
perchlorate
MA
various
grades
substrates
into
up
40
%
benzoic
acid
BAc
),
formic
FA
small
proportions
acetophenone
ACP
under
visible
light
(456
nm)
through
solar
radiation.
Time‐resolved
emission
absorption
spectroscopy
evidence
reaction
with
oxygen
primary
photochemical
step
in
oxygen‐saturated
solutions,
accounting
for
77
photons
absorbed
vs.
1
direct
(0.303
M
repeating
units).
These
results
are
agreement
mechanism
which
‐mediated
photo
occurs
abstraction
benzylic
H
atoms
reactive
generated
energy
electron
transfer
from
excited
state
Addition
triplet
O
2
these
radicals,
followed
intra‐
inter‐molecular
hydrogen
atom
(HAT)
generates
C‐
O‐centered
radicals
then
undergoing
β‐scission
hydroperoxide
fragmentation.
The
formation
intermediate
oligomers
functionalized
terminal
carbonyl
groups
demonstrated
both
infrared
analysis
MALDI
TOF
mass
spectrometry.
undergo
further
photoinduced
conversion
even
absence
,
as
evidenced
size
exclusion
chromatography
irradiated
samples.
Language: Английский
Reassessing the Photochemical Upcycling of Polystyrene Using Acridinium Salts
Angewandte Chemie,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 13, 2024
Abstract
Polystyrene
(
PS
)
is
a
commodity
plastic
recalcitrant
to
chemical
recycling
or
upcycling
processes.
Approaches
aimed
at
deconstructing
by
photocatalytic
means
struggle
generate
high‐energy
species
capable
of
cleaving
the
robust
C−H
and
C−C
bonds
.
We
show
that
9‐mesityl‐10‐methylacridinium
perchlorate
MA
various
grades
substrates
into
up
40
%
benzoic
acid
BAc
),
formic
FA
small
proportions
acetophenone
ACP
under
visible
light
(456
nm)
through
solar
radiation.
Time‐resolved
emission
absorption
spectroscopy
evidence
reaction
with
oxygen
primary
photochemical
step
in
oxygen‐saturated
solutions,
accounting
for
77
photons
absorbed
vs.
1
direct
(0.303
M
repeating
units).
These
results
are
agreement
mechanism
which
‐mediated
photo
occurs
abstraction
benzylic
H
atoms
reactive
generated
energy
electron
transfer
from
excited
state
Addition
triplet
O
2
these
radicals,
followed
intra‐
inter‐molecular
hydrogen
atom
(HAT)
generates
C‐
O‐centered
radicals
then
undergoing
β‐scission
hydroperoxide
fragmentation.
The
formation
intermediate
oligomers
functionalized
terminal
carbonyl
groups
demonstrated
both
infrared
analysis
MALDI
TOF
mass
spectrometry.
undergo
further
photoinduced
conversion
even
absence
,
as
evidenced
size
exclusion
chromatography
irradiated
samples.
Language: Английский