Green Chemistry,
Год журнала:
2021,
Номер
23(11), С. 4065 - 4073
Опубликована: Янв. 1, 2021
The
dissolution
and
further
alkaline
hydrolysis
of
PET
in
biomass-derived
γ-valerolactone
is
realized
at
a
relatively
mild
temperature
high
efficiency.
Polymer Journal,
Год журнала:
2024,
Номер
56(4), С. 249 - 268
Опубликована: Янв. 12, 2024
Abstract
Over
8
billion
tons
of
plastic
have
been
produced
to
date,
and
a
100%
reclamation
recycling
strategy
is
not
foreseeable.
This
review
summarizes
how
the
mechanochemistry
polymers
may
contribute
sustainable
polymer
future
by
controlling
degradation
only
de
novo
developed
designer
but
also
plastics
in
existing
waste
streams.
The
historical
development
presented
while
highlighting
current
examples
mechanochemically
induced
degradation.
Additionally,
theoretical
computational
frameworks
are
discussed
that
lead
discovery
better
understanding
new
mechanochemical
reactions
future.
takes
into
account
technical
engineering
perspectives
converging
fields
trituration
with
particular
focus
on
fate
commodity
potential
technologies
monitor
they
occur.
Therefore,
unique
perspective
multiple
communities
presented,
need
for
transdisciplinary
research
tackle
high-leverage
parameters
governing
an
eventually
successful
approach
circular
economy.
Nature Chemistry,
Год журнала:
2024,
Номер
16(7), С. 1184 - 1192
Опубликована: Апрель 12, 2024
Abstract
Polymers
that
degrade
on
demand
have
the
potential
to
facilitate
chemical
recycling,
reduce
environmental
pollution
and
are
useful
in
implant
immolation,
drug
delivery
or
as
adhesives
debond
demand.
However,
polymers
made
by
radical
polymerization,
which
feature
all
carbon-bond
backbones
constitute
most
important
class
of
polymers,
proven
difficult
render
degradable.
Here
we
report
cyclobutene-based
monomers
can
be
co-polymerized
with
conventional
impart
resulting
mechanically
triggered
degradability.
The
cyclobutene
residues
act
mechanophores
undergo
a
ring-opening
reaction,
causes
rearrangement
renders
polymer
chains
cleavable
hydrolysis
under
basic
conditions.
These
broadly
applicable
free
controlled
polymerizations,
introduce
functional
groups
into
backbone
allow
gated
degradation
high-molecular-weight
materials
cross-linked
networks
low-molecular-weight
species.
Polymers,
Год журнала:
2025,
Номер
17(5), С. 628 - 628
Опубликована: Фев. 26, 2025
The
growing
environmental
impact
of
textile
waste,
fueled
by
the
rapid
rise
in
global
fiber
production,
underscores
urgent
need
for
sustainable
end-of-life
solutions.
This
review
explores
cutting-edge
pathways
waste
management,
spotlighting
innovations
that
reduce
reliance
on
incineration
and
landfilling
while
driving
material
circularity.
It
highlights
advancements
collection,
sorting,
pretreatment
technologies,
as
well
both
established
emerging
recycling
methods.
Smart
collection
systems
utilizing
tags
sensors
show
great
promise
streamlining
logistics
automating
pick-up
routes
transactions.
For
automated
technologies
like
near-infrared
hyperspectral
imaging
lead
way
accurate
scalable
separation.
Automated
disassembly
techniques
are
effective
at
removing
problematic
elements,
though
other
pretreatments,
such
color
finish
removal,
still
to
be
customized
specific
streams.
Mechanical
is
ideal
textiles
with
strong
mechanical
properties
but
has
limitations,
particularly
blended
fabrics,
cannot
repeated
endlessly.
Polymer
recycling-through
melting
or
dissolving
polymers-produces
higher-quality
recycled
materials
comes
high
energy
solvent
demands.
Chemical
recycling,
especially
solvolysis
pyrolysis,
excels
breaking
down
synthetic
polymers
polyester,
potential
yield
virgin-quality
monomers.
Meanwhile,
biological
methods,
their
infancy,
natural
fibers
cotton
wool.
When
methods
not
viable,
gasification
can
used
convert
into
synthesis
gas.
concludes
future
hinges
integrating
sorting
advancing
solvent-based
chemical
technologies.
These
innovations,
supported
eco-design
principles,
progressive
policies,
industry
collaboration,
essential
building
a
resilient,
circular
economy.
Abstract
Converting
poly(ethylene
terephthalate)
(PET)
into
metal–organic
frameworks
(MOFs)
has
emerged
as
a
promising
innovation
for
upcycling
of
waste
plastics.
However,
previous
solvothermal
methods
suffer
from
toxic
solvent
consumption,
long
reaction
time,
high
pressure,
and
temperature.
Herein,
mechanochemical
milling
strategy
was
reported
to
transform
PET
series
MOFs
with
yields.
This
had
the
merits
solvent‐free
conditions,
ambient
temperature,
short
running
easy
scale‐up
large‐scale
production
MOFs.
The
as‐prepared
exhibited
definite
crystal
structure
porous
morphology
composed
agglomerated
nanoparticles.
It
proven
that,
under
milling,
firstly
decomposed
1,4‐benzenedicarboxylate,
which
acted
linkers
coordinate
metal
ions
forming
fragments,
followed
by
gradual
arrangement
fragments
work
not
only
promotes
value‐added
conversion
polyesters
but
also
offers
new
opportunity
produce
in
green
scalable
manner.
Waste
polyester
textiles
are
not
recycled
due
to
separation
challenges
and
partial
structural
degradation
during
use
recycling.
Chemical
recycling
of
polyethylene
terephthalate
(PET)
through
depolymerization
can
provide
a
feedstock
monomers
make
"as-new"
polymers.
While
enzymatic
PET
is
more
selective
sustainable
approach,
methods
in
development,
however,
have
thus
far
been
limited
clean,
high-quality
feedstocks,
require
an
energy-intensive
melt-amorphization
step
ahead
treatment.
Here,
high-crystallinity
mixed
PET/cotton
could
be
directly
selectively
depolymerized
terephthalic
acid
(TPA)
by
using
commercial
cutinase
from
Humicola
insolens
under
moist-solid
reaction
conditions,
affording
up
30±2
%
yield
TPA.
The
process
was
readily
combined
with
cotton
simultaneous
or
sequential
application
the
cellulase
enzymes
CTec2®,
providing
83±4
glucose
without
any
negative
influence
on
TPA
yield.
Nature Communications,
Год журнала:
2023,
Номер
14(1)
Опубликована: Янв. 14, 2023
Polymers
with
low
ceiling
temperatures
(Tc)
are
highly
desirable
as
they
can
depolymerize
under
mild
conditions,
but
typically
suffer
from
demanding
synthetic
conditions
and
poor
stability.
We
envision
that
this
challenge
be
addressed
by
developing
high-Tc
polymers
converted
into
low-Tc
on
demand.
Here,
we
demonstrate
the
mechanochemical
generation
of
a
polymer,
poly(2,5-dihydrofuran)
(PDHF),
an
unsaturated
polyether
contains
cyclobutane-fused
THF
in
each
repeat
unit.
Upon
mechanically
induced
cycloreversion
cyclobutane,
unit
generates
three
units
PDHF.
The
resulting
PDHF
completely
depolymerizes
2,5-dihydrofuran
presence
ruthenium
catalyst.
otherwise
difficult-to-synthesize
highlights
power
polymer
mechanochemistry
accessing
elusive
structures.
concept
mechanochemically
regulating
Tc
applied
to
develop
next-generation
sustainable
plastics.
ACS Materials Au,
Год журнала:
2024,
Номер
4(3), С. 335 - 345
Опубликована: Март 18, 2024
Polyester
fibers,
comprising
mostly
poly(ethylene
terephthalate)
with
high
crystalline
content,
represent
the
most
commonly
produced
plastic
for
ubiquitous
textiles,
and
approximately
60
million
tons
are
manufactured
annually
worldwide.
Considering
social
issues
of
mismanaged
waste
from
used
textile
products,
there
is
an
urgent
demand
sustainable
polyester
fiber
recycling
methods.
We
developed
a
low-temperature,
rapid,
efficient
depolymerization
method
fibers.
By
utilizing
methanolysis
dimethyl
carbonate
as
trapping
agent
ethylene
glycol,
fibers
products
proceeded
at
50
°C
2
h,
affording
terephthalate
(DMT)
in
>90%
yield.
This
strategy
allowed
us
to
depolymerize
even
practical
textiles
blended
other
selectively
isolate
DMT
yields.
was
also
applicable
colored
analytically
pure
isolated
via
decolorization
processes.