- By:
- Zheng, Jackie ; Boucher, Mairead F; Galan, Nicholas J; Danielson, Mary K; Rahman, Md Anisur ; McConnell, David J; Bowland, Christopher C; Barnett, Philip R; Saito, Tomonori
- Journal Name:
- ACS Materials Letters
- Page Number:
- 868-873
- Volume:
- 8
- Issue Number:
- 3
- Publication Date:
- March 16, 2026
- View DOI Listing:
- https://doi.org/10.1021/acsmaterialslett.5c01543
Abstract
Nylon-based fiber-reinforced composites are widely used in various sectors due to their strength, durability, and lightweight properties. Despite their widespread use, recycling these composites is difficult due to the inability to separate fibers and thermal instability of nylon at high temperatures. Consequently, most nylon composites are landfilled, leading to significant economic loss. Current fiber recovery methods (i.e., pyrolysis) are energetically inefficient and preclude recovery of the matrix. Dissolution methods, such as using hexafluoroisopropanol (HFIP), allow recovery of polymer and fiber but are economically taxing and require extensive safety infrastructure. Herein we report tailored glycolysis of nylon-6 composites, resulting in separated constituent fibers and nylon-6 oligomers. Deconstruction kinetics reveal nylon’s molecular weight reductions from 32,600 to 2000 g/mol, while SEM and tensile testing confirm recovered fiber integrity. This approach offers a pathway to reclaim high-value materials from nylon composites, providing a strategy for the chemical recycling of fiber-reinforced composites.
