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Self-curing Epoxy Resin as a Bio-based Adhesive for Wood Products (PPT)

机译:自固化环氧树脂作为木制品的生物基粘合剂(PPT)

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1. The utilization of two different HTL-bio-oils (W-HTL-bio-oii and WE-HTL-bio-oil) was investigated for the synthesis of epoxy resin. 2. The distribution of OH groups within bio-oi! (aliphatic, phenolic and acidic OH) plays an important role on the yield and EEW of epoxy resin. 3. Curing kinetics and FT-IR analysis revealed that curing of BOBER was mainly controlled by etherification reaction. 4. DMA analysis showed that BOBER-WE had a higher storage modulus (845 MPa), glass transition temperature (96 °C), and crosslink density (58.7 mol/m3) than BOBER-W (425 MPa, 63.6 °C, and 8.5 mol/m3), suggesting that addition of ethanol in HTL process improved the thermomecrsanical properties of epoxy resin. 5. Lab shear test showed that bio-oil based epoxy resins are comparable to the commercial epoxy resin in dry and wet conditions.
机译:1.研究了两种不同的HTL-生物油(W-HTL-BIO-OII和We-HTL-Bio-油)以合成环氧树脂。 2. Bio-oi内OH群体的分布! (脂族,酚类和酸性OH)对环氧树脂的产率和EEW起着重要作用。 3.固化动力学和FT-IR分析表明,通过醚化反应来控制自由的固化。 4. DMA分析表明,BOWS-WE具有更高的储存模量(845MPa),玻璃化转变温度(96℃)和交联密度(58.7mol / m3),而不是BOL-W(425MPa,63.6°C和8.5 mol / m3),表明在HTL过程中添加乙醇改善了环氧树脂的热致植物性质。 5.实验室剪切试验表明,生物油基环氧树脂与在干燥和湿润条件下的商业环氧树脂相当。

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