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Thermal properties and micromorphology of polyurethane resins based on liquefied benzylated wood

机译:液化苄基化木材的聚氨酯树脂的热性能和微观形态

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Liquefied benzylated wood based Polyurethanes (PUs) are synthesized with excess toluene diisocyanate (TDI), isophorone diisocyanate (IPDI) and hexamethylene diisocyanate (HDI). Four polyethylene glycols (PEG) of molecular weight 400, 600, 1000 and 2000 are mixed with liquefied wood using dibasic ester (DBE) as liquefaction reagent to incorporate different proportions of soft segment into the network prior to crosslinking with TDI. By differential scanning calorimetry, thermogravimetry, wide angle X-ray diffraction and SEM analysis, thermal properties and micromorphology of PU samples are investigated. Results indicated that molecular weight of the PEG had only a minor effect on glass transition temperature (T_g) of PU samples, but diisocyanates had major effects. The T_gg of HDI-based PU network was -25℃ lower than that of TDI (40℃) and IPDI (28.6℃). From SEM analysis, TDI, IPDI-based films have better phase-mixing properties than HDI-based PU. All the films had greater thermal stability than conventional PU films based on polyether or polyester alone.
机译:用过量的甲苯二异氰酸酯(TDI),异佛尔酮二异氰酸酯(IPDI)和六亚甲基二异氰酸酯(HDI)合成液化的苄基木基聚氨酯(PU)。使用二元酸酯(DBE)作为液化试剂,将四种分子量分别为400、600、1000和2000的聚乙二醇(PEG)与液化木材混合,以在与TDI交联之前将不同比例的软链段掺入网络中。通过差示扫描量热,热重分析,广角X射线衍射和SEM分析,研究了PU样品的热性能和微观形貌。结果表明,PEG的分子量对PU样品的玻璃化转变温度(T_g)影响不大,而二异氰酸酯的影响最大。基于HDI的PU网络的T_gg比TDI(40℃)和IPDI(28.6℃)低-25℃。根据SEM分析,基于TDI,IPDI的薄膜比基于HDI的PU具有更好的相混合特性。与仅基于聚醚或聚酯的常规PU膜相比,所有膜均具有更高的热稳定性。

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