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Acid-base-catalyzed two-step liquefaction of empty fruit bunch lignin residue for preparation of biopolyol and high-performance biopolyurethanes

机译:酸碱催化的两步液化空果束木质素残留物,用于制备生物多聚酚和高性能生物聚氨基乙烷

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摘要

To reduce the dependence on fossil fuel, empty fruit bunch (EFB) lignin residue, a waste material generated from second-generation lignocellulosic biomass was used for the production of biopolyol and biopolyurethanes. The acid-base-catalyzed two-step liquefaction process was carried out to drive residual lignin into value-added products. The reaction condition for the second step (base-catalyzed liquefaction) was optimized to reduce molecular weight and lower the acid number below 5 mg KOH/g for preparing more suitable biopolyol. The optimal condition was determined at 2 wt% of catalyst loading and 130 degrees C reaction temperature for a reaction time of 60 min. By employing the upgraded two-step liquefaction process, biopolyol with a molecular weight of 4724 g/mol, a viscosity of 1.14 Pa s and a hydroxyl number of 816 mg KOH/g was obtained from low-grade lignin. The resulting biopolyol was converted to biopolyurethane elastomer and biopolyurethane foam with p-TDI and p-MDI as isocyanate, respectively. The biopolyurethane elastomer exhibited a high temperature at 10% weight loss T-d10 of 318 degrees C and temperature at 50% weight loss T-d50 of 386 degrees C. Besides, the biopolyurethane foam possesses a compressive strength and density of 99 kPa and 24.8 kg/m(3), which are properties comparable with petroleum-derived polyurethane.
机译:为了减少对化石燃料的依赖性,空果脯束(EFB)木质素残留物,从第二代木质纤维素生物量产生的废料用于生产生物聚醇和生物聚氨基乙烷。进行酸基催化的两步液化过程,以将残留的木质素驱动成增值产物。优化第二步(碱催化液化)的反应条件,以减少分子量,降低5mg KOH / g的酸数,以制备更合适的生物聚溶胶。在2wt%的催化剂负载下测定最佳条件,并为60分钟的反应时间为130℃的反应温度。通过采用升级的两步液化过程,从低级木质素中获得了分子量为4724g / mol的粘度为1.14pa的粘度和羟基数为816mg KOH / g的粘度。将所得杀菌溶胶与P-TDI和P-MDI转化为生物聚氨基乙烷弹性体和生物聚氨酯泡沫,分别为异氰酸酯。生物聚氨酸弹性体在318℃的10%重量损失T-D10下表现出高温,50%重量损失T-D50的温度为386℃。此外,生物聚氨酯泡沫具有抗压强度和99kPa的密度和24.8 Kg / m(3),其是与石油衍生的聚氨酯相当的性质。

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  • 来源
    《Wood Science and Technology》 |2021年第2期|315-330|共16页
  • 作者单位

    Kyung Hee Univ Dept Chem Engn Integrated Engn Seoul Gyeonggi Do South Korea;

    Kyung Hee Univ Dept Chem Engn Integrated Engn Seoul Gyeonggi Do South Korea;

    Kyung Hee Univ Dept Chem Engn Integrated Engn Seoul Gyeonggi Do South Korea;

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  • 入库时间 2022-08-19 01:18:01
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