Renewable Lactam Monomer for Tunable and Processable Polyamides

Replacement of petroleum-derived monomers with renewable alternatives is an integral part of the sustainable polymer framework. Research in this area involves the search for bio-based or recycled starting materials for traditional polymers, as well as investigations into new materials accessible from renewable feedstocks. Focusing on the latter, we studied the properties of polyamides synthesized from γ-methyl-ε-caprolactam through anionic ring-opening polymerization by an activated monomer mechanism. The amorphous homopolymer presents high stiffness (Young’s modulus, ≈3 GPa), strength (stress at break, ≈80 MPa) and toughness under dry (low humidity) conditions, high ductility (strain at break, ≈1100%) in humid environments, optical clarity, and excellent processability due to its non-crystallizable nature and solubility in common organic solvents. Copolymerization with ε-caprolactam allows tailoring the mechanical properties and crystallinity in the resultant copolymers and provides new opportunities for advanced manufacturing and other applications.

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Publication Details

Journal
Macromolecules
Published
2025-03-14
DOI
https://doi.org/10.1021/acs.macromol.4c03199
Citations
3
Primary Topic
biodegradable polymer synthesis and properties
Type
article
Field-Weighted Citation Impact
1.79

Funders

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article

Renewable Lactam Monomer for Tunable and Processable Polyamides

Satu Häkkinen, Daniel M. Krajovic, Marc A. Hillmyer, William R. Dichtel et al.
3 citations
Macromolecules
biodegradable polymer synthesis and properties
1.79
article

Renewable Lactam Monomer for Tunable and Processable Polyamides

Satu Häkkinen, Daniel M. Krajovic, Marc A. Hillmyer, William R. Dichtel, Arpan Biswas, Kari M. Chamberlain, Honghu Zhang, Lillian M. Felsenthal, Joshua Shippee
article en
3 citations

Abstract

Replacement of petroleum-derived monomers with renewable alternatives is an integral part of the sustainable polymer framework. Research in this area involves the search for bio-based or recycled starting materials for traditional polymers, as well as investigations into new materials accessible from renewable feedstocks. Focusing on the latter, we studied the properties of polyamides synthesized from γ-methyl-ε-caprolactam through anionic ring-opening polymerization by an activated monomer mechanism. The amorphous homopolymer presents high stiffness (Young’s modulus, ≈3 GPa), strength (stress at break, ≈80 MPa) and toughness under dry (low humidity) conditions, high ductility (strain at break, ≈1100%) in humid environments, optical clarity, and excellent processability due to its non-crystallizable nature and solubility in common organic solvents. Copolymerization with ε-caprolactam allows tailoring the mechanical properties and crystallinity in the resultant copolymers and provides new opportunities for advanced manufacturing and other applications.

MacromoleculesVol. 58(6)
Northwestern University (US), University of Minnesota (US), Brookhaven National Laboratory (US), University of Minnesota System (US), Stanford Synchrotron Radiation Lightsource (US), National Synchrotron Light Source II
Division of Chemistry
Affordable and clean energy
Openalex Percentile: Top 17%
biodegradable polymer synthesis and properties
1.79
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Renewable Lactam Monomer for Tunable and Processable Polyamides — Satu Häkkinen, Daniel M. Krajovic, et al. · Macromolecules (2025) | TGRS Research Map | TGRS