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Stereocomplex PLLA–PBAT copolymer and its composites with multi-walled carbon nanotubes for electrostatic dissipative application
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Abstract
Because of its low thermal stability and brittleness, both the drawbacks of poly(
l
-lactide) (PLLA) were solved by forming stereocomplex (ST) and its copolymer with poly(butylene adipate-
co
-terephthalate) (PLLA–PBAT). In this study, we synthesized PLLA and PLLA–PBAT copolymer by ring-opening polymerization. Both polymers were blended with poly(
d
-lactide) to form ST crystals. Multi-walled carbon nanotubes (MWCNTs) were added into the polymer matrix at 5 phr by the solvent casting method. The surface resistance of the composite was ≅10
6
Ω, which is appropriate for electrostatic dissipative purposes. The copolymer and its ST crystallites were confirmed by the peaks in infrared spectra at 922 and 908 cm
−1
, respectively. The PLLA–PBAT copolymer had 60% lower tensile strength than PLLA and its stereocomplex, but 10% higher elongation at break. The elongation at break of the PLLA–PBAT copolymer/MWCNT composite decreased by 17% while its thermal stability slightly increased when compared to the unfilled copolymer. The melting temperature for both ST PLLA–PBAT copolymers, with and without MWCNTs, was around 225°C, which is 50°C higher than that of the homocrystals. Moreover, the glass transition temperature and crystallinity of the ST PLLA–PBAT copolymer also increased by adding MWCNTs.
Walter de Gruyter GmbH
Title: Stereocomplex PLLA–PBAT copolymer and its composites with multi-walled carbon nanotubes for electrostatic dissipative application
Description:
Abstract
Because of its low thermal stability and brittleness, both the drawbacks of poly(
l
-lactide) (PLLA) were solved by forming stereocomplex (ST) and its copolymer with poly(butylene adipate-
co
-terephthalate) (PLLA–PBAT).
In this study, we synthesized PLLA and PLLA–PBAT copolymer by ring-opening polymerization.
Both polymers were blended with poly(
d
-lactide) to form ST crystals.
Multi-walled carbon nanotubes (MWCNTs) were added into the polymer matrix at 5 phr by the solvent casting method.
The surface resistance of the composite was ≅10
6
Ω, which is appropriate for electrostatic dissipative purposes.
The copolymer and its ST crystallites were confirmed by the peaks in infrared spectra at 922 and 908 cm
−1
, respectively.
The PLLA–PBAT copolymer had 60% lower tensile strength than PLLA and its stereocomplex, but 10% higher elongation at break.
The elongation at break of the PLLA–PBAT copolymer/MWCNT composite decreased by 17% while its thermal stability slightly increased when compared to the unfilled copolymer.
The melting temperature for both ST PLLA–PBAT copolymers, with and without MWCNTs, was around 225°C, which is 50°C higher than that of the homocrystals.
Moreover, the glass transition temperature and crystallinity of the ST PLLA–PBAT copolymer also increased by adding MWCNTs.
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