Abstract
Kraft lignin (KL) and castor oil (CO) were used as polyols in the synthesis of bio-based polyurethanes (PUs) in the absence of both solvents and catalysts at room temperature with simultaneous film formation. KL was purified (PKL), and both KL and PKL were fully characterized. CO was mixed with different percentages of PKL (0%, 10%, 30%, and 50%), as well as with polymeric methyl phenyl diisocyanate. After degassing, the reaction mixture was stirred; when the medium viscosity was suitable for spreading, it was poured onto a glass plate, and the thickness was adjusted using an extender. The storage modulus (E′, 25 °C) and tensile strength of the lignopolyurethane films (LignoPUCOPKL) were higher than those of the control film (PUCO). LignoPUCOPKL30 and LignoPUCOPKL50 did not break under the conditions that the other films broke under. It was noted phase segregation (rigid and flexible domains) for LignoPUCOPKL30 and LignoPUCOPKL50, and the glass transition temperature (Tg) of the flexible domains (96.2 °C and 52.3 °C, respectively) was higher than that of PUCO (8.4 °C). The formed films were also characterized by scanning electron microscopy, thermogravimetric analysis, X-ray diffraction, contact angles, and swelling tests. To our knowledge, the approach of this study is unprecedented.
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More From: International Journal of Biological Macromolecules
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