Synthesis and characteristics of α-carboxylic, ω-hydroxyl natural rubber toughened poly(lactic acid)
Abdulhakim Masa, Varaporn Tanrattanakul, Ruedee Jaratrotkamjorn
Vol. 17., No.11., Pages 1121-1134, 2023
DOI: 10.3144/expresspolymlett.2023.85
DOI: 10.3144/expresspolymlett.2023.85
GRAPHICAL ABSTRACT

ABSTRACT
This work presented the synthesis of α-carboxyl, ω-hydroxyl natural rubber (CHNR) for use as an alternative toughening agent for poly(lactic acid) (PLA). The proton nuclear magnetic resonance spectroscopy (1H-NMR) and Fourier transform infrared spectroscopy (FTIR) analyses verified the chemical structure of CHNR consisting of the hydroxyl and carboxyl end groups. The molecular weights of CHNR were set from 5000 to 15 000 g·mol–1 which were determined by gel permeation chromatography (GPC) and 1H-NMR. The PLA and CHNR were prepared by reactive blending using a twinscrew extruder. It was found that the reaction between PLA and CHNR proceeded through transesterification without a catalyst. The formation of copolymer (PLA-co-CHNR) at the interface of PLA and CHNR increased the interfacial adhesion between the two phases. Differential scanning calorimetry (DSC) analysis revealed that CHNR was more compatible with PLA than natural rubber (NR). The compatibilization affected the blend morphology by reducing the interfacial tension. It resulted in a reduction of rubber particle size. The CHNR with a molecular weight of 5000 g·mol–1 showed the greatest improvement in the toughness and ductility of PLA.
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This is an editorial article. It has no abstract.
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DOI: 10.3144/expresspolymlett.2024.29

The
effect of swelling and plasticizer content of a plastic, as well as the ethanol
content of the food simulant on the migration kinetics of three stabilizer-type
additives from polylactic acid (PLA)-based food contact plastics has been
investigated. The results proved that the parameters that affect the diffusion
of substances inside the polymer matrix, i.e.,
swelling, plasticization, and the size of migrants, are the decisive factors in
the migration from PLA to ethanolic food simulants. Both swelling and migration
were negligible when ethanol 10% (v/v) was used. Contrarily, the specific
migration limits of Commission Regulation (European Union, EU) No. 10/2011 were
exceeded in ethanol 50% (v/v) for all investigated stabilizers. Migration was
promoted by plasticization, but this effect could only be observed when the
applied food simulant swelled the plastic (at least 20% (v/v) ethanol content).
The dependence of the plasticizer’s migration-enhancing effect on the swelling
has not been shown before. When the plasticization caused increased migration,
it also led to specific migration limit exceeding within a shorter period of
time. It happens even if PLA-based plastics are dedicated to the storage of
hydrophilic food, which is the most common application area of these products.
These results can support the improvement of both consumer safety and active
packaging development.