Block Compositions and Microstructure‐Macroproperty Regulation of Biobased Long Carbon‐Chain Polyamide Elastomers

Long carbon-chain polyamide elastomers (LCPAEs), an emerging class of high-performance elastomers, have garnered widespread interest due to their excellent flexibility, exceptional low/high temperature resistance, and favorable physical and mechanical properties. In this work, we systematically investigated the influence of block compositions (relative content and molecular chain length of hard segment (HS) and soft segments (SS)) on the microstructural and macroscopic properties of the LCPAEs with gradient HS contents (ca. 20-70 wt.%) by various characterization techniques. The results show that increasing HS content generally leads to better crystallization ability, higher thermal stability, greater mechanical strength (reduced ductility), more pronounced microphase separation morphology, and varied shape memory effect. These findings highlight the feasibility of tailoring LCPAEs' chemical structures and properties through modulating the relative content of HS and SS precisely. More importantly, the quantitative correlations between the block compositions and mechanical properties of LCPAEs were established via using the average distance between adjacent HS domains (L) and the average constrained molecular weight between physical cross-linking junctions ( <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"> <mml:semantics> <mml:msub><mml:mover><mml:mi>M</mml:mi> <mml:mo>¯</mml:mo></mml:mover> <mml:mi>C</mml:mi></mml:msub> <mml:annotation>${{\overline M }_C}$</mml:annotation></mml:semantics> </mml:math> ) as the bridge (the correlation coefficients R<sup>2</sup> of both L and <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"> <mml:semantics> <mml:msub><mml:mover><mml:mi>M</mml:mi> <mml:mo>¯</mml:mo></mml:mover> <mml:mi>C</mml:mi></mml:msub> <mml:annotation>${{\overline M }_C}$</mml:annotation></mml:semantics> </mml:math> with tensile strength are greater than 0.99), which helps to guide the precise structural design and property directional control of high-performance LCPAEs.

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Publication Details

Journal
Macromolecular Rapid Communications
Published
2025-08-25
DOI
https://doi.org/10.1002/marc.202500493
Citations
1
Primary Topic
biodegradable polymer synthesis and properties
Type
article
Field-Weighted Citation Impact
0.60

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article

Block Compositions and Microstructure‐Macroproperty Regulation of Biobased Long Carbon‐Chain Polyamide Elastomers

Kai Pan, Changhai Cao, Biao Zhao, Jin Cheng et al.
1 citations
Macromolecular Rapid Communications
biodegradable polymer synthesis and properties
0.60
article

Block Compositions and Microstructure‐Macroproperty Regulation of Biobased Long Carbon‐Chain Polyamide Elastomers

Kai Pan, Changhai Cao, Biao Zhao, Jin Cheng, Yi Zhang, Shun Gong, Yidi Wang
article en
1 citations

Abstract

Long carbon-chain polyamide elastomers (LCPAEs), an emerging class of high-performance elastomers, have garnered widespread interest due to their excellent flexibility, exceptional low/high temperature resistance, and favorable physical and mechanical properties. In this work, we systematically investigated the influence of block compositions (relative content and molecular chain length of hard segment (HS) and soft segments (SS)) on the microstructural and macroscopic properties of the LCPAEs with gradient HS contents (ca. 20-70 wt.%) by various characterization techniques. The results show that increasing HS content generally leads to better crystallization ability, higher thermal stability, greater mechanical strength (reduced ductility), more pronounced microphase separation morphology, and varied shape memory effect. These findings highlight the feasibility of tailoring LCPAEs' chemical structures and properties through modulating the relative content of HS and SS precisely. More importantly, the quantitative correlations between the block compositions and mechanical properties of LCPAEs were established via using the average distance between adjacent HS domains (L) and the average constrained molecular weight between physical cross-linking junctions ( <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"> <mml:semantics> <mml:msub><mml:mover><mml:mi>M</mml:mi> <mml:mo>¯</mml:mo></mml:mover> <mml:mi>C</mml:mi></mml:msub> <mml:annotation>${{\overline M }_C}$</mml:annotation></mml:semantics> </mml:math> ) as the bridge (the correlation coefficients R<sup>2</sup> of both L and <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"> <mml:semantics> <mml:msub><mml:mover><mml:mi>M</mml:mi> <mml:mo>¯</mml:mo></mml:mover> <mml:mi>C</mml:mi></mml:msub> <mml:annotation>${{\overline M }_C}$</mml:annotation></mml:semantics> </mml:math> with tensile strength are greater than 0.99), which helps to guide the precise structural design and property directional control of high-performance LCPAEs.

Macromolecular Rapid CommunicationsVol. 46(21)
Sinopec (China) (CN), Beijing University of Chemical Technology (CN)
China Petrochemical Corporation
Openalex Percentile: Top 30%
biodegradable polymer synthesis and properties
0.60
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