Angewandte Chemie,
Journal Year:
2024,
Volume and Issue:
136(44)
Published: Aug. 6, 2024
Abstract
The
development
of
mechanically
robust,
chemically
stable,
and
yet
recyclable
polymers
represents
an
essential
undertaking
in
the
context
advancing
a
circular
economy
for
plastics.
Here,
we
introduce
novel
cleavable
β‐(1,3‐dioxane)ester
(
DXE
)
linkage,
synthesized
through
catalyst‐free
reaction
β‐ketoester
1,3‐diol,
to
cross‐link
poly(vinyl
alcohol)
PVA
formation
high‐performance
thermosets
with
inherent
chemical
recyclability.
,
modified
groups
transesterification
excess
tert
‐butyl
acetoacetate,
undergoes
cross‐linking
reactions
unmodified
1,3‐diols
within
itself
upon
thermal
treatment.
architecture
improves
’s
mechanical
properties,
Young's
modulus
toughness
that
can
reach
up
656
MPa
84
MJ
cm
−3
i.e.
approximately
3‐
12‐fold
those
linear
respectively.
Thermal
treatment
cross‐linked
under
acid
conditions
leads
deconstruction
networks,
enabling
excellent
recovery
(>90
%)
.
In
absence
either
or
acidic
treatment,
maintains
its
dimensional
stability.
We
show
is
also
possible
when
performed
presence
other
plastics
commonly
found
recycling
mixtures.
Furthermore,
‐based
composites
comprising
carbon
fibers
activated
charcoal
by
linkages
are
shown
be
fillers.
Journal of the American Chemical Society,
Journal Year:
2024,
Volume and Issue:
146(18), P. 12645 - 12655
Published: April 23, 2024
The
increased
production
of
plastics
is
leading
to
the
accumulation
plastic
waste
and
depletion
limited
fossil
fuel
resources.
In
this
context,
we
report
a
strategy
create
polymers
that
can
undergo
controlled
depolymerization
by
linking
renewable
feedstocks
with
siloxane
bonds.
α,ω-Diesters
α,ω-diols
containing
bonds
were
synthesized
from
an
alkenoic
ester
derived
castor
oil
then
polymerized
varied
monomers,
including
related
biobased
monomers.
addition,
cyclic
monomers
hydrosiloxanes
prepared
cyclized
form
26-membered
macrolactone
unit.
Sequential
ring-opening
polymerization
lactide
afforded
ABA
triblock
copolymer.
This
set
siloxanes
underwent
programmed
into
in
protic
solvents
or
hexamethyldisiloxane
acid
catalyst.
Monomers
polyesters
linkages
repolymerized
demonstrate
circularity
select
polymers.
Evaluation
environmental
stability
these
toward
enzymatic
degradation
showed
they
hydrolysis
fungal
cutinase
Fusarium
solani.
soil
microbial
metabolism
selectively
labeled
13C
revealed
differential
main
chain
side
organic
groups
microbes.
Macromolecules,
Journal Year:
2024,
Volume and Issue:
57(7), P. 3407 - 3415
Published: April 1, 2024
Functionalization
of
polyethylene
toward
high-performance
polymers
with
good
thermal
and
mechanical
properties
is
a
persistent
challenge.
Closo-carboranes,
polyhedral
nanocage
structure,
provide
excellent
chemical
stability.
In
this
work,
main-chain
carborane-embedded
prepared
by
the
ring-opening
metathesis
copolymerization
cyclic
o-carborane
olefin
cyclooctene,
followed
backbone
hydrogenation.
The
mimics
could
offer
superior
to
high-density
(HDPE)
adjusting
incorporation
ratio
while
still
maintaining
moderate
crystalline
properties.
ACS Nano,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 21, 2025
The
development
of
bioplastics
is
advancing
globally
to
promote
a
sustainable
society.
In
this
study,
we
designed
cellulosic
dual-network
address
the
need
for
materials
with
balanced
mechanical
properties
and
biodegradability.
Cellulose
was
used
as
first
network,
second
network
functionalized
enhance
strength
while
preserving
dynamic
covalent
moieties
within
were
generated
through
dithiolane
ring-opening
polymerization.
ultimate
tensile
flexural
elongation
controlled
8.8-193
MPa
3.3-32.5%,
respectively,
depending
on
degree
bonds.
Moreover,
exhibited
gradual
biodegradability,
achieving
approximately
30%
degradation
2
weeks.
Interestingly,
our
demonstrated
ability
coexist
plants,
their
did
not
negatively
affect
cell
viability
or
plant
growth.
This
study
provides
promising
approach
developing
advanced
that
reach
sustainability
goals
offering
tunable
properties.
Research Square (Research Square),
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 25, 2025
Abstract
The
pursuit
of
clean
and
sustainable
energy
sources
has
intensified
the
research
focus
on
water
electrolysis,
particularly
oxygen
evolution
reaction
(OER),
which
serves
as
a
pivotal
step
in
hydrogen
generation.
However,
development
efficient
cost-effective
OER
catalysts
remains
major
bottleneck
hindering
widespread
adoption
electrolysis
technology.
In
this
work,
utilizing
vermiculite
(VMT),
an
abundant
environmentally
friendly
clay
mineral,
was
employed
precursor
to
obtain
SiO2(V-SiO2).
We
have
successfully
synthesized
novel
phosphate-modified
layered
nickel
silicate
Ni3Si2O5(OH)4
(NiSi-P)
derived
from
VMT
through
combination
hydrothermal
vapor
deposition
method.
Electrochemical
evaluations
1.0
M
KOH
revealed
that
NiSi-P
exhibited
remarkable
performance,
achieving
low
overpotential
334
mV
at
10
mA·cm-2,
significantly
outperforming
unmodified
(NiSi,
564
mV).
This
improvement
is
attributed
unique
structural
features
surface
chemistry
NiSi-P,
facilitate
charge
transfer
protonation/deprotonation
during
catalytic
process.
study
provided
idea
for
application
low-cost
materials
electrocatalytic
splitting
OER.
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
63(44)
Published: Aug. 6, 2024
Abstract
The
development
of
mechanically
robust,
chemically
stable,
and
yet
recyclable
polymers
represents
an
essential
undertaking
in
the
context
advancing
a
circular
economy
for
plastics.
Here,
we
introduce
novel
cleavable
β‐(1,3‐dioxane)ester
(
DXE
)
linkage,
synthesized
through
catalyst‐free
reaction
β‐ketoester
1,3‐diol,
to
cross‐link
poly(vinyl
alcohol)
PVA
formation
high‐performance
thermosets
with
inherent
chemical
recyclability.
,
modified
groups
transesterification
excess
tert
‐butyl
acetoacetate,
undergoes
cross‐linking
reactions
unmodified
1,3‐diols
within
itself
upon
thermal
treatment.
architecture
improves
’s
mechanical
properties,
Young's
modulus
toughness
that
can
reach
up
656
MPa
84
MJ
cm
−3
i.e.
approximately
3‐
12‐fold
those
linear
respectively.
Thermal
treatment
cross‐linked
under
acid
conditions
leads
deconstruction
networks,
enabling
excellent
recovery
(>90
%)
.
In
absence
either
or
acidic
treatment,
maintains
its
dimensional
stability.
We
show
is
also
possible
when
performed
presence
other
plastics
commonly
found
recycling
mixtures.
Furthermore,
‐based
composites
comprising
carbon
fibers
activated
charcoal
by
linkages
are
shown
be
fillers.
ACS Macro Letters,
Journal Year:
2024,
Volume and Issue:
unknown, P. 1704 - 1710
Published: Dec. 7, 2024
Recovering
monomers
from
the
depolymerization
of
thermosets
presents
a
significant
challenge,
which
becomes
even
more
daunting
if
one
sets
goal
doing
it
directly,
i.e.,
without
complex
chemical
separation
steps.
To
this
end,
we
have
synthesized
new
type
polycarbonate
thermoset
by
first
copolymerizing
alkyl
cyclic
carbonates
(ACCs)
with
small
amounts
allyloxy
(AoCCs),
followed
cross-linking
resulting
excess
tetrathiol
compounds
under
UV
irradiation.
These
cross-linked
polycarbonates
demonstrate
enhanced
thermal
and
mechanical
properties
compared
to
their
linear
analogues,
while
maintaining
polymers'
capacity
for
ring-closing
depolymerization.
The
process
enables
direct
recovery
ACC
its
dimer,
bypassing
steps
that
are
commonly
employed
in
recycling
conventional
chemically
recyclable
thermosets.
yields
range
74.7%
91.7%
depending
on
ratios
AoCC
Furthermore,
recovered
can
be
repolymerized
AoCCs
leading
same
quality
initially
one.