ACS Sustainable Chemistry & Engineering,
Journal Year:
2024,
Volume and Issue:
12(44), P. 16165 - 16174
Published: Oct. 21, 2024
Previous
studies
aiming
to
achieve
sustainability
in
adhesive
materials,
primarily
focused
on
the
integration
of
bioderived
or
biodegradable
components.
However,
existing
sustainable
adhesives
often
prioritize
permanent
adhesion
over
removability,
which
limits
their
recyclability.
Herein,
we
introduce
an
innovative
approach
for
producing
scalable,
biodegradable,
and
removable
hot-melt
adhesives,
offering
sustainability.
Polybutylene
succinate
(PBS)
was
selected
as
base
polymer
because
its
excellent
melt
processability,
biodegradability,
commercial
availability.
To
impart
adhesiveness,
three
biomass-derived
tackifiers
were
incorporated;
basic
rosin,
disproportionated
rosin
ester.
The
use
a
twin-screw
extruder
enabled
efficient
mixing
large-scale
production
at
kilogram
scale.
Our
investigation
revealed
that
exhibited
optimal
compatibility
wettability,
attributed
high
acid
value.
value
promoted
rapid
crystallization
minimized
crystal
defects.
A
correlation
between
behavior
strength
also
established,
identifying
composition.
composition
yields
satisfactory
(2.5
N/25
mm)
makes
it
suitable
repositionable
adhesives.
Additionally,
our
optimized
sufficient
biodegradability
completely
decomposed
by
lipase
within
21
d,
has
not
been
observed
previous
studies.
This
study
provides
practical
pathway
enhancing
with
potential
further
advancements
tailoring
diverse
applications
future
research.
Macromolecular Rapid Communications,
Journal Year:
2024,
Volume and Issue:
45(17)
Published: June 2, 2024
As
the
demand
for
sustainable
polymers
increases,
most
research
efforts
have
focused
on
polyesters,
which
can
be
bioderived
and
biodegradable.
Yet
analogous
polythioesters,
where
one
of
oxygen
atoms
has
been
replaced
by
a
sulfur
atom,
remain
relatively
untapped
source
potential.
The
incorporation
allows
polymer
to
exhibit
wide
range
favorable
properties,
such
as
thermal
resistance,
degradability,
high
refractive
index.
Polythioester
synthesis
represents
frontier
in
research,
holding
promise
paving
way
eco-friendly
alternatives
conventional
polyesters.
Moreover,
polythioester
also
open
avenues
development
recyclable
materials.
In
last
25
years,
many
methods
synthesize
polythioesters
developed.
However,
date
no
industrial
developed
due
challenges
costs,
yields,
toxicity
by-products.
This
review
will
summarize
recent
advances
synthesis,
covering
step-growth
polymerization,
ring-opening
polymerization
(ROP),
biosynthesis.
Crucially,
benefits
processes
highlighted,
paying
particular
attention
their
sustainability,
with
aim
encouraging
further
exploration
into
fast-growing
field
polythioesters.
ChemPlusChem,
Journal Year:
2024,
Volume and Issue:
89(6)
Published: Feb. 21, 2024
With
the
increasing
use
of
pressure-sensitive
adhesives
(PSAs)
in
various
industries,
there
is
a
need
for
greater
sustainability,
particularly
developing
polymer
materials
from
renewable
resources,
as
well
reuse
and
recycling
to
reduce
environmental
impact,
waste,
or
extend
their
life.
Here,
we
outlined
required
properties
PSAs
which
are
governed
by
molecular
parameters
(molecular
weights,
dispersities,
weight
between
entanglement,
cross-links
gel
content)
subsequently
define
physical
(storage
loss
moduli,
glass
transition
temperature)
that
good
performance
peel,
tack
shear
tests.
The
sustainable
approach
discussed
here
development
degradable
featuring
selectively
linkages
backbone.
This
provides
viable
alternative
design
could
overcome
'stickies'
problem
make
cardboard
more
efficient.
Polymer,
Journal Year:
2024,
Volume and Issue:
302, P. 127032 - 127032
Published: April 8, 2024
Radical
ring-opening
(co)polymerization
(RROP)
provides
an
accessible
method
for
synthesizing
main
chain
degradable
vinyl
polymers.
Although
the
applications
of
reversible
deactivation
radical
polymerization
(RDRP)
into
RROP
have
been
reported,
use
photo-mediated
RDRP
methods
has
received
less
attention
than
thermal
process.
Here,
photo-RROP
thionolactone
dibenzo[c,e]-oxepine-5(7H)-thione
(DOT)
and
methyl
acrylate
(MA)
was
studied
using
photo-iniferter
(PI)
addition-fragmentation(chain)
transfer
(RAFT)
at
ambient
temperature
without
external
initiators
or
photocatalysts.
Despite
occurrence
some
side
reactions
including
desulfurization-oxygenation
O-S
isomerization
DOT
promoted
by
photoexcited
thiocarbonyl
groups,
polymers
with
thioester
linkages
in
backbone
were
prepared,
which
degraded
presence
amines
bleach.
Macromolecules,
Journal Year:
2023,
Volume and Issue:
56(23), P. 9787 - 9795
Published: Nov. 30, 2023
The
thionolactone
3,3-dimethyl-2,3-dihydro-5H-benzo[e][1,4]dioxepine-5-thione
(DBT)
is
shown
to
radically
homopolymerize,
copolymerize
rapidly
with
acrylates
and
styrene,
and,
for
the
first
time,
methacrylates,
introducing
a
degradable
thioester
backbone
functionality.
Surprisingly,
aminolysis
of
DBT
homopolymers
was
accompanied
by
intramolecular
ether
cleavage,
leading
formation
2,2-dimethylthiirane
salicylamides.
rapid
copolymerization
styrene
exploited
produce
copolymers
through
free-radical
polymerization
in
starve-fed
semibatch
setup.
higher
reactivity
compared
current
benchmark
dibenzo[c,e]oxepine-5(7H)-thione
(DOT)
inconsistent
expected
electron-donating
effect
alkoxy
substituent
DBT.
Using
single-crystal
XRD
structure
analysis
DFT
modeling,
this
study
rationalized
(i)
better
stabilization
intermediate
radical
means
overlap
adjacent
aromatic,
which
shifts
addition
equilibrium
right;
(ii)
an
increased
ring
strain
DOT,
drives
ring-opening;
(iii)
reinitiating
efficiency
tertiary
alkyl
open-ring
benzylic
DOT.
These
insights
are
facilitate
development
further
monomers
tailored
behavior.
Macromolecular Chemistry and Physics,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 20, 2025
Abstract
This
work
investigates
the
correlation
between
formulation
of
waterborne
acrylic
pressure‐sensitive
adhesives
(PSAs)
and
their
resulting
adhesive
performance.
A
library
n
‐butyl
acrylate‐based
latexes
is
synthesized
via
miniemulsion
polymerization.
Controlled
variations
in
composition
these
polyacrylates
–
such
as
inclusion
rigid
comonomers,
latent
crosslinkers
chain
transfer
agents
enabled
precise
control
over
key
network
structures
particles
leading
then
to
a
range
physical
parameters
cast
PSA
films
glass
transition
temperature,
entanglement
crosslink
density.
The
viscoelastic
mechanical
behaviors
networks
are
carefully
characterized
using
combination
techniques,
including
linear
rheology,
dynamic
analysis,
tensile
testing.
These
properties
correlated
with
performance,
measured
by
probe
tack
shear
holding
time
tests.
comprehensive
approach
allowed
for
identification
optimal
balance
that
delivers
best
compromises
directly
correlating
outcomes
macromolecular
design.
Polymer-based
particulate
materials
are
useful
in
various
industries,
but
nondegradable
polymeric
that
generate
microplastics
pose
challenges.
Herein,
we
synthesized
main-chain
degradable
polymer
particles
by
radical
ring-opening
polymerization
(rROP)
a
miniemulsion
system
(miniemulsion
rROP),
which
dibenzo[c,e]oxepan-5-thione
(DOT)
was
selected
as
the
monomer.
Miniemulsion
rROP
of
DOT
and
typical
vinyl
comonomers
(styrene:
St
n-butyl
acrylate:
nBA)
performed.
The
rate
significantly
higher
than
solution
rROP.
feed
molar
ratio
increased
to
20
mol
%
with
high
conversion.
Colloidally
stable
poly(St-DOT)
were
successfully
degraded
amine
compounds
homogeneous
heterogeneously
dispersed
systems.
Additionally,
when
nBA
used
monomer,
colloidally
poly(nBA-DOT)
synthesized,
their
degradation
observed
n-propylamine,
evidencing
possibility
using
synthesize
particles.
Journal of Applied Polymer Science,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 26, 2025
ABSTRACT
Renewable
and
degradable
pressure‐sensitive
adhesives
(PSAs)
have
emerged
as
promising
green
alternatives
in
the
adhesive
industry,
addressing
both
petroleum
resource
depletion
plastic
pollution
challenges.
This
work
is
to
provide
a
design
preparation
of
high‐performance
biodegradable
bio‐based
thermoplastic
polyurethane
adhesive(TPU‐PSAs)
solve
problem
that
most
PSAs
are
nondegradable,
nonrenewable,
nonrecyclable.
Through
solvent‐free
one‐step
polymerization
process,
we
synthesized
TPU‐PSAs
using
polylactide
diol
(PLA),
polycaprolactone
(PCL),
polytetramethylene
ether
glycol
(PTMEG)
polyols
with
varying
NCO/OH
ratios.
correlation
analysis
microphase
separation
morphology,
viscoelastic
response,
macroscopic
adhesion
behavior,
structure‐performance
relationship
system
was
established,
which
promoted
rational
sustainable
adhesives.
Notably,
HS
(30)/0.8
(NCO/OH
=
0.8)
demonstrated
exceptional
peel
strength
(7.5
N/cm)
coupled
substantial
biodegradability
(56.4%
degradation
within
8
weeks).
Meanwhile,
(30)/1
1)
exhibited
superior
shear
resistance
(368
kPa
on
glass
substrates)
without
requiring
cross‐linking
agents.
These
showcase
unique
combination
tunable
properties
through
controlled
separation,
positioning
them
candidates
for
applications
demand
biodegradability,
recyclability,
renewability.