Evolution of Copolymers of Epoxides and CO2: Catalysts, Monomers, Architectures, and Applications
Chemical Reviews,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 25, 2024
The
copolymerization
of
CO
Language: Английский
Closed-loop recyclable polymers: from monomer and polymer design to the polymerization–depolymerization cycle
Shuaiqi Yang,
No information about this author
Shuai Du,
No information about this author
Jin Zhu
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et al.
Chemical Society Reviews,
Journal Year:
2024,
Volume and Issue:
53(19), P. 9609 - 9651
Published: Jan. 1, 2024
We
present
the
state-of-the-art
of
circular
polymers
based
on
monomer
and
polymer
design
reversible
ring-opening
addition
polymerization
reactions
without
involvement
other
reactants.
Language: Английский
Multifunctional bio-aerogels realized by solvophilic phase assisted phase separation for passive radiative cooling and energy harvesting
Yameng Wang,
No information about this author
Feifei Zhang,
No information about this author
Zewei Hou
No information about this author
et al.
Chemical Engineering Journal,
Journal Year:
2025,
Volume and Issue:
unknown, P. 162059 - 162059
Published: April 1, 2025
Language: Английский
Soft‐Segment Containing Lignin‐Based Polyhydroxyurethanes: Controllable Flexibility Through PDMS Integration
Lily Masa,
No information about this author
Arijit Ghorai,
No information about this author
Hoyong Chung
No information about this author
et al.
Macromolecular Rapid Communications,
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 7, 2025
Abstract
Lignin,
a
biomass‐derived
polymer,
is
rich
in
aromatic
groups
composed
of
phenylpropane
units,
providing
rigidity,
thermal
stability,
and
mechanical
strength
ideal
for
structural
applications.
However,
its
inherent
stiffness
limits
flexibility.
To
address
this,
lignin
copolymerized
with
bis(3‐aminopropyl)‐terminated
poly(dimethylsiloxane)
(PDMS‐NH
2
),
introducing
tunable
elasticity
improved
properties.
Lignin
first
modified
CO₂
to
produce
cyclic
carbonate‐functionalized
(CCL).
The
CCL
reacts
PDMS‐NH
amines
via
the
ring‐opening
carbonates,
forming
soft‐hard
polyhydroxyurethane
copolymers
adjustable
properties
(CCL‐PDMS‐PHUs).
Structural
characterization
confirms
urethane
bond
formation,
peaks
at
1680
cm⁻¹
(FT‐IR)
chemical
shifts
161.33
ppm
(¹
3
C
NMR)
7.99
(¹H
NMR).
Thermal
analysis
reveals
5%
decomposition
temperatures
246–265
°C
glass
transition
(Tg)
ranging
from
44
66
°C,
indicating
stability.
Mechanical
testing
shows
that
CCL‐PDMS‐PHU60
(60%
)
exhibited
greater
softness,
while
CCL‐PDMS‐PHU40
(40%
displayed
higher
stiffness,
highlighting
’s
effect
on
These
results
demonstrate
CCL‐PDMS‐PHUs
offer
customizable
properties,
making
them
promising
materials
applications
requiring
tailored
performance.
Language: Английский