A promising strategy for fabricating high-performance stereocomplex-type polylactide products via carbon nanotubes-assisted low-temperature sintering
01 natural sciences
0104 chemical sciences
DOI:
10.1016/j.polymer.2018.12.032
Publication Date:
2018-12-24T16:36:20Z
AUTHORS (6)
ABSTRACT
Abstract Recently, powder metallurgy inspired low-temperature (below the melting temperature) sintering has been proposed as an innovative technology for the processing of eco-friendly stereocomplex-type polylactide (SC-PLA) from its nascent powder, without triggering noticeable thermal degradation. The physicochemical performances of the obtained SC-PLA products are governed by the newly formed SC crystallites with a remarkable ability to weld the interfaces between adjacent powder particles, however, the insufficient interdiffusion of poly(L-lactide) (PLLA) and poly(D-lactide) (PDLA) chains across the interfaces makes it challenging to form sufficient amounts of new SC crystallites. In the present work, we describe a facile and robust strategy to address this challenge by coating a trace amount (e.g., 0.001 wt%) of disentangled carbon nanotubes (CNTs) on the SC-PLA particle surfaces. During the subsequent sintering, these interface-localized CNTs can function as efficient nucleating agent to substantially promote the SC crystallization of PLLA/PDLA chains on their surfaces and finally countless SC crystallites are formed to strongly weld the interfaces as welded joints. Accordingly, SC-PLA/CNTs products possessing superb heat/solvent resistances and mechanical strength have been fabricated. Impressively, with the introduction of 0.001 wt% CNTs, the tensile strength is significantly enhanced from 45.8 MPa to 67.2 MPa. Most importantly, there is a linear relationship between the tensile strength and the content of the CNTs induced SC crystallites. Overall, this wok could provide a practical guidance for the design and fabrication of high-performance SC-PLA products through low-temperature sintering assisted by nanofillers like CNTs.
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