Structure–Property Relationships of Elastomeric Vinylogous Urethane Thermosets and Their Application as Closed-Loop Recyclable Strain Sensors
Macromolecules,
Journal Year:
2025,
Volume and Issue:
58(4), P. 1923 - 1934
Published: Feb. 5, 2025
Developing
closed-loop
recyclable
thermosets
and
understanding
their
structure–property
relationships
are
essential
steps
in
advancing
a
circular
materials
economy.
Here,
we
present
vinylogous
urethane
(VU)
thermoset
with
recyclability,
synthesized
through
the
reaction
of
polytetrahydrofuran
bisacetoacetate
(aPTHF)
tris(2-aminoethyl)amine
(TREN).
These
VU
polymers
exhibit
high
elasticity,
only
3–9%
residual
strain
observed
after
cyclic
tensile
testing
at
maximum
100%,
depending
on
molecular
weight
aPTHF
network
cross-link
density.
The
two
structural
parameters
also
allow
modulation
mechanical
stress-relaxation
properties
elastomers.
To
investigate
hydrolysis
linkages
within
hydrophobic
matrix,
employed
heterogeneous
system
using
biphasic
mixture
HCl
CDCl3.
Our
findings
show
that
VUs
remain
stable
pure
water
but
can
be
dissociated
under
acidic
conditions,
dissociation
rate
accelerated
higher
temperatures
and/or
presence
concentrations.
detailed
investigations
indicate
potential
elastomers
as
sustainable
substrates
for
wearable
sensors.
We
therefore
conduct
case
study
synthesizing
sensor
incorporation
multiwalled
carbon
nanotubes
(MCNs)
into
elastomer
matrix.
robustly
detect
various
movements.
Moreover,
treatment
both
neat
polymer
composite
diethyl
ether
solvent
allows
excellent
recovery
(>90%)
TREN
(86%),
without
discernible
damage
to
MCNs
reclaimed
from
latter.
Language: Английский
Next-generation solar energy: Progress, stability, and prospects of polymer-modified Perovskite solar cells; A review
Pei Zhang,
No information about this author
Huanggen Yang,
No information about this author
Qi Zheng
No information about this author
et al.
International Journal of Hydrogen Energy,
Journal Year:
2025,
Volume and Issue:
106, P. 1088 - 1113
Published: Feb. 8, 2025
Language: Английский
Recent Advances in the Chemical Recycling of Polyamide for a Sustainable Circular Economy
Industrial & Engineering Chemistry Research,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 27, 2025
Language: Английский
Linear and Network-Forming Acetal Polymerization of Multifunctional Alcohols with Dichloromethane for Degradable and Recyclable Materials
Macromolecules,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 29, 2025
Language: Английский
Ultratough Thermoplastic Elastomers Based on Chemically Recyclable Cycloalkyl-Substituted Polyhydroxyalkanoates
Journal of the American Chemical Society,
Journal Year:
2025,
Volume and Issue:
147(9), P. 7788 - 7798
Published: Feb. 20, 2025
It
remains
a
long-standing
challenge
for
chemical
recycling
of
polyhydroxyalkanoates
(PHAs)
to
propiolactone-based
monomers
due
the
high
ring
strain
and
many
inevitable
side
reactions.
In
this
contribution,
novel
α-spiro-cyclohexyl-propiolactone
(SHPL)
has
been
designed
with
reactivity
toward
ring-opening
polymerization
even
at
catalyst
loading
<1
ppm.
The
resulting
poly(3-hydroxy-2-spiro-cyclohexylpropionate)
(P3HSHP)
exhibited
thermal
stability
Td
364
°C
Tm
272
°C.
Meanwhile,
it
could
be
depolymerized
back
SHPL
in
86%
yield
without
decarboxylation
or
elimination
products.
Notably,
exploited
construct
high-performance
thermoplastic
elastomers
(TPEs)
via
one-pot
copolymerization
ε-caprolactone
(CL).
Particularly,
gradient
P(CL2000-grad-SHPL500)
showcased
an
ultimate
tensile
strength
58.8
±
4.0
MPa,
stretchability
1959
53%,
record
toughness
600
MJ/m3,
elastic
recovery
(>90%).
This
superior
performance
advance
development
new
sustainable
TPEs.
Language: Английский
Clusterization-triggered room-temperature phosphorescent synthetic polymeric materials
Wenya Yan,
No information about this author
Peixuan Dong,
No information about this author
Qiyu Zhang
No information about this author
et al.
Coordination Chemistry Reviews,
Journal Year:
2025,
Volume and Issue:
535, P. 216629 - 216629
Published: March 28, 2025
Language: Английский
Synergetic “amine scissors” break down cured epoxy resins with nearly 100% degradation efficiency
Furong Xie,
No information about this author
Rong Chen,
No information about this author
Chao Deng
No information about this author
et al.
Chemical Engineering Journal,
Journal Year:
2025,
Volume and Issue:
unknown, P. 161175 - 161175
Published: March 1, 2025
Language: Английский
Viscoelastic Supramolecular Networks Based on Guanidinium‐Oxyanion Interactions
Oliver G. Venablerose,
No information about this author
Evan B. Van Pelt,
No information about this author
Ava L. DeKoekkoek
No information about this author
et al.
Journal of Polymer Science,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 25, 2025
ABSTRACT
We
describe
the
synthesis
and
characterization
of
supramolecular
networks
based
on
charge‐assisted
hydrogen
bonding
interactions
guanidinium
oxyanion
functionalities.
Although
they
are
constructed
entirely
small‐molecule
components,
these
materials
display
properties
such
as
a
glass
transition
time‐
temperature‐dependent
viscoelastic
rheological
behavior.
These
can
be
tuned
by
choice
each
network
component:
T
g
varies
over
50°C
in
studied
networks,
relaxation
times
scaled
with
changes
to
.
However,
inherently
degradable
thermally
reversible
no
covalent
macromolecular
structure
is
formed.
Language: Английский
Direct Monomer Recovery from Ring-Closing Depolymerization of Thermosets
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.
Language: Английский