Rapid Microwave-Assisted Chemical Recycling of Poly(p-Phenylene Terephthalamide)
Joël Benninga,
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B. Gebben,
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Rudy Folkersma
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et al.
Journal of the American Chemical Society,
Journal Year:
2025,
Volume and Issue:
147(9), P. 7191 - 7195
Published: Feb. 21, 2025
Back-to-monomer
chemical
recycling
of
polymers
is
crucial
in
achieving
a
circular
plastics
economy.
Herein,
we
report
the
rapid
microwave-assisted
depolymerization
poly(p-phenylene
terephthalamide)
(PPTA),
also
known
as
Twaron
or
Kevlar.
The
alkaline
hydrolysis
PPTA
was
conducted
microwave
reactor
at
temperatures
ranging
from
240
to
260
°C
with
reaction
times
1-15
min.
highest
conversion
(96%)
found
after
15
min
°C.
resulting
monomers
terephthalic
acid
and
p-phenylenediamine
were
successfully
purified
(>99%
purity)
good
yields
using
extraction
precipitation
methods.
This
work
presents
fastest
date
under
relatively
mild
conditions,
thereby
encouraging
value
chain
for
PPTA.
Language: Английский
Zinc-Oxide-Supported Zeolite Subcrystal Catalyst: Enhancing Chemical Recycling of Poly(lactic acid) via Optimized Active Site Dispersion and Polymer Diffusion
Ling Ding,
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Di Pan,
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Ke Du
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et al.
ACS Sustainable Chemistry & Engineering,
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 2, 2025
Language: Английский
Hydrogen-Bond-Network-Driven Biodegradable PLA Elastomer with High Strength and Toughness
Yuzhu Zhai,
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Sidra Ghaffar,
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Yongxin Zhao
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et al.
ACS Applied Polymer Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 21, 2025
Language: Английский
Polyester transesterification through reactive blending and its applications: a comprehensive review
Polymer,
Journal Year:
2025,
Volume and Issue:
unknown, P. 128488 - 128488
Published: May 1, 2025
Language: Английский
Robust, Thermally Stable and Impurity-Tolerant Aluminum-Based Catalyst System for Polylactide Production under Industrial Conditions
Ze-Bin Wang,
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Mingqian Wang,
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Zhiqiang Ding
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et al.
Polymer science & technology.,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 4, 2024
Ring-opening
polymerization
of
l-lactide
(l-LA)
is
a
powerful
approach
that
leverages
renewable
monomer
to
generate
high-molecular-weight
polylactide
(PLA).
It
essential
replace
the
industrially
used
cytotoxic
tin(II)
bis(2-ethylhexanoate)
[Sn(Oct)2]
with
low/nontoxic
alternatives.
However,
most
benign
catalysts
addressed
solution
polymerizations
are
typically
performed
at
25–100
°C.
Robust,
thermally
stable
and
protonic
agent-tolerant
for
industrial
PLA
production
still
lacking.
Herein,
we
designed
synthesized
tetracoordinate
aluminum
methyl
complexes
bearing
(amidoalkyl)pyridine–phenolate
(AmPyPh)
pincers
l-LA
polymerizations.
The
catalytic
activity
could
be
modulated
by
electronic
steric
effects
substituents
in
different
positions.
structure–catalytic
performance
relationships
were
further
investigated
assistance
density
functional
theory
calculations.
These
(AmPyPh)AlMe
effectively
promote
under
industrial-relevant
conditions
(150–180
°C,
melt
bulk).
novel
Al
suppress
epimerization
side
reaction
harsh
afforded
semicrystalline
PLLA.
molecular
weight
monomer/catalyst
feed
ratio
loading
dosage
chain
transfer
agent.
showed
comparable
Sn(Oct)2
presence
20
equiv
benzyl
alcohol
but
exhibited
much
higher
degree
control
over
PLLA
narrower
distribution.
Technical
grade
without
purification
also
polymerized
rapidly
thanks
good
tolerance
agents
high
temperature.
Language: Английский