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Polydopamine surface modified Ti 3 C 2 T x / PLA biocomposites with enhanced mechanical, thermal, and tribological properties
The industry desires to create robust, resilient, thermally stable, and environmentally friendly composites. In this study, we created a poly (lactic acid) (PLA) composite via a straightforward method. The Ti 3 C 2 T X was surface‐coated with polydopamine (PDA) via a bioinspired approach and was the...
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Published in: | Journal of applied polymer science 2023-11, Vol.140 (44) |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | The industry desires to create robust, resilient, thermally stable, and environmentally friendly composites. In this study, we created a poly (lactic acid) (PLA) composite via a straightforward method. The Ti
3
C
2
T
X
was surface‐coated with polydopamine (PDA) via a bioinspired approach and was then reinforced in the PLA using melt blending. The PDA layer adorned on the Ti
3
C
2
T
X
provided several functional groups for the MXene nanosheets and strengthened the PLA‐MXene interaction by hydrogen bonding. The well‐dispersed PDA@Ti
3
C
2
T
X
in the PLA improved mechanical, thermal, and tribological properties. For PLA/PDA@Ti
3
C
2
T
X
‐1, the tensile strength and elongation at the break of the nano‐composite were 9.03% and 25.5% higher than pure PLA, respectively. The flexural strength and modulus were increased by 49.5% over pure PLA, reaching 148.8 and 6702 MPa, respectively. The nanocomposite toughness increased by up to 53.3%. The nanocomposites had 3.8% and 49.08% lower friction coefficient and specific wear rate, respectively, than pure PLA. The addition of Ti
3
C
2
T
X
and PDA@Ti
3
C
2
T
X
increased the thermal stability of PLA at lower temperatures and promoted carbonization. PLA/PDA@Ti
3
C
2
T
X
‐1 showed the maximum char yield of 10 wt.% at 800°C, proving the highest thermal barrier effect due to MXene exfoliation during PDA and increased PLA dispersion state. |
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ISSN: | 0021-8995 1097-4628 |
DOI: | 10.1002/app.54619 |