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Thermal and Mechanical Properties of Polyurethanes Derived from Fractionated Kraft Lignin.

1997; Volume: 53; Issue: 10 Linguagem: Inglês

10.2115/fiber.53.10_416

1884-2259

Junzö Nakano, Yoshinobu Izuta, Tomomi Orita, Hyōe Hatakeyama, Ken Kobashigawa, Kiichi Teruya, Shigeo Hirose,

Polymer composites and self-healing

Polyurethane (PU) sheets were prepared from fractionated kraft lignin (KL) samples having molecular weights (MW's) of 1420 and 860, polyethylene glycol having a MW of 400 (PEG 400) and diphenylmethane diisocyanate (MDI). KL contents in weight %, in a mixture of KL and PEG 400, were varied from 10 to 50%. The thermal and mechanical properties of PU's were studied by thermogravimetry (TG), differential scanning calorimetry (DSC) and tensile tests. The thermal decomposition temperatures slightly decreased with increasing KL contents. The glass transition temperatures (Tg's) increased, the temperature range of glass transition (ΔT) increased, and the heat capacity difference between the glass and rubbery states at Tg's (ΔCp) decreased, with increasing KL contents. Tensile properties such as strength at break (σ), elongation at break (ε), and Young's modulus (E) were measured at 25°C. The obtained results were highly dependent on the state, i.e. the glassy state and the rubbery state. The effect of molecular weight of KL on thermal degradation and tensile properties was not prominent. However, Tg's apparently increased with decreasing molecular weights of KL when the same amounts in weight % of KL were introduced into PU molecules.