Here we report the synthesis of thermosetting resins from low molar mass Kraft lignin fractions of high functionality, re-fined by solvent extraction. Such fractions were fully characterized by 31P-NMR, 2D-HSQC NMR, SEC and DSC in order to obtain a detailed description of the structures. Reactive oxirane moieties were introduced on the lignin backbone under mild reaction conditions and quantified by simple 1H-NMR analysis. The modified fractions were chemically cross-linked with a flexible polyether diamine (Mn≈2000), in order to obtain epoxy thermosets. Epoxies from different lignin fractions, studied by DSC, DMA, tensile tests and SEM, demonstrated substantial differences in terms of thermo-mechanical prop-erties. For the first time, strong relationships between lignin structures and epoxy properties could be demonstrated. The suggested approach provides unprecedented possibilities to tune network structure and properties of thermosets based on real lignin fractions, rather than model compounds.

Enzyme catalysed ring-opening polymerisation was performed by reactive extrusion gave high molecular weight polyester ( M _w ≥ 163 000 g mol ⁻¹ ) in 15 minutes.