Vat photopolymerization (VP) is a rapidly growing additive manufacturing technology (3D-printing), yet its reliance on fossil-derived and potentially hazardous acrylate resins presents a significant sustainability challenge. Although itaconic acid has emerged as a promising bio-based platform chemical, current synthetic strategies to functionalize it often involve toxic intermediates and energy-intensive processes. This work reports a sustainable route for the synthesis of a novel class of itaconamide monomers derived from essential amino acids (alanine, valine, isoleucine, and phenylalanine) via the direct, solvent-minimised ring-opening of itaconic anhydride. This approach avoids chlorinated reagents and activation steps, aligning with green chemistry principles. The monomers were incorporated into photocurable formulations (up to 40 mol%), demonstrating highly tunable mechanical properties: aliphatic derivatives acted as efficient plasticizers, increasing elongation at break by up to 385%, while phenylalanine moieties provided network reinforcement via pi-pi interactions. Thermal analysis confirmed stable glass transition temperatures combined with enhanced char yields. Crucially, a quantitative sustainability assessment yielded a Sustainable Formulation Score (SFS) of up to 51.8, significantly outperforming current state of the art bio-based resins. The successful fabrication of high-resolution 3D printed objects confirms these materials as viable, high-performance, and eco-friendly candidates for VP.
Carmenini, R., Capancioni, F., Maturi, M., Locatelli, E., Molina, S.I., Sambri, L., et al. (2026). Sustainable itaconamide monomers from amino acids for vat photopolymerization 3D printing. RSC SUSTAINABILITY, 4(4), 1857-1866 [10.1039/d6su00014b].
Sustainable itaconamide monomers from amino acids for vat photopolymerization 3D printing
Carmenini R.;Capancioni F.;Locatelli E.;Sambri L.;Comes Franchini M.
2026
Abstract
Vat photopolymerization (VP) is a rapidly growing additive manufacturing technology (3D-printing), yet its reliance on fossil-derived and potentially hazardous acrylate resins presents a significant sustainability challenge. Although itaconic acid has emerged as a promising bio-based platform chemical, current synthetic strategies to functionalize it often involve toxic intermediates and energy-intensive processes. This work reports a sustainable route for the synthesis of a novel class of itaconamide monomers derived from essential amino acids (alanine, valine, isoleucine, and phenylalanine) via the direct, solvent-minimised ring-opening of itaconic anhydride. This approach avoids chlorinated reagents and activation steps, aligning with green chemistry principles. The monomers were incorporated into photocurable formulations (up to 40 mol%), demonstrating highly tunable mechanical properties: aliphatic derivatives acted as efficient plasticizers, increasing elongation at break by up to 385%, while phenylalanine moieties provided network reinforcement via pi-pi interactions. Thermal analysis confirmed stable glass transition temperatures combined with enhanced char yields. Crucially, a quantitative sustainability assessment yielded a Sustainable Formulation Score (SFS) of up to 51.8, significantly outperforming current state of the art bio-based resins. The successful fabrication of high-resolution 3D printed objects confirms these materials as viable, high-performance, and eco-friendly candidates for VP.| File | Dimensione | Formato | |
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d6su00014b.pdf
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d6su00014b1.pdf
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