Liu Guifeng, Jin Can, Huo Shuping, Kong Zhenwu, Chu Fuxiang
Institute of Chemical Industry of Forest Products, CAF, Nanjing 210042, China; National Engineering Lab. for Biomass Chemical Utilization, Nanjing 210042, China; Key Lab. of Chemical Engineering of forest Products, National Forestry and Grassland Administration, Nanjing 210042, China; Key Lab. of Biomass Energy and Material of Jiangsu Province, Nanjing 210042, China; Co-Innovation Center of Efficient Processing and Utilization of Forest Resources of Jiangsu Province, Nanjing 210037, China.
Institute of Chemical Industry of Forest Products, CAF, Nanjing 210042, China; National Engineering Lab. for Biomass Chemical Utilization, Nanjing 210042, China; Key Lab. of Chemical Engineering of forest Products, National Forestry and Grassland Administration, Nanjing 210042, China; Key Lab. of Biomass Energy and Material of Jiangsu Province, Nanjing 210042, China; Co-Innovation Center of Efficient Processing and Utilization of Forest Resources of Jiangsu Province, Nanjing 210037, China.
Int J Biol Macromol. 2021 Dec 15;193(Pt B):1400-1408. doi: 10.1016/j.ijbiomac.2021.10.203. Epub 2021 Nov 3.
A series of lignin-based epoxy resins (LEPs) were prepared by the reaction of epichlorohydrin with lignin oligomers derived from partial reductive depolymerization of lignin. To overcome the high viscosity and brittleness defects in practical applications, the LEPs were blended with renewable epoxied cardanol glycidyl ether (ECGE) and then cured with methyltetrahydrophthalic anhydride (MeTHPA) to form high-performance epoxy thermosets. The effects of degree of lignin depolymerization, chemical composition of lignin oligomers and dosage of ECGE on thermal and mechanical properties of the cured products were investigated. The LEP/MeTHPA thermosets exhibited good thermal and mechanical properties. Especially, by separating monomer-rich fractions from lignin oligomers, the thermal and mechanical properties of the cured product were improved obviously. Notably, the incorporation of ECGE also possessed a positive effect on reinforcing and toughening the cured products. With 20 wt% ECGE loadings, the tensile, flexural and impact strength of the cured product reached the maximum value of 77 MPa, 115 MPa and 14 kJ/m, respectively, which were equivalent to the commercial bisphenol A epoxy resins thermosets. These findings indicated that the novel bio-based epoxy resins from lignin oligomers and cardanol could be utilized as renewable alternatives for BPA epoxy resins.
通过环氧氯丙烷与木质素部分还原解聚得到的木质素低聚物反应,制备了一系列木质素基环氧树脂(LEP)。为克服实际应用中高粘度和脆性的缺陷,将LEP与可再生的环氧腰果酚缩水甘油醚(ECGE)共混,然后用甲基四氢苯酐(MeTHPA)固化,形成高性能环氧热固性材料。研究了木质素解聚程度、木质素低聚物的化学组成以及ECGE用量对固化产物热性能和力学性能的影响。LEP/MeTHPA热固性材料表现出良好的热性能和力学性能。特别是,通过从木质素低聚物中分离出富含单体的馏分,固化产物的热性能和力学性能得到明显改善。值得注意的是,加入ECGE对固化产物的增强和增韧也有积极作用。当ECGE含量为20 wt%时,固化产物的拉伸强度、弯曲强度和冲击强度分别达到最大值77 MPa、115 MPa和14 kJ/m,与商用双酚A环氧树脂热固性材料相当。这些研究结果表明,由木质素低聚物和腰果酚制备的新型生物基环氧树脂可作为双酚A环氧树脂的可再生替代品。