六亚甲基四胺
苯酚
化学
木质素
差示扫描量热法
水解
玻璃化转变
极限抗拉强度
聚合
固化(化学)
酚类
复合数
热固性聚合物
核化学
有机化学
聚合物
高分子化学
复合材料
材料科学
物理
热力学
作者
Yongsheng Zhang,Zhongshun Yuan,Nubla Mahmood,Shanhua Huang,Chunbao Xu
标识
DOI:10.1016/j.indcrop.2015.10.048
摘要
In this study a bio-based novolac resin, bio-phenol-hydroxymethylfurfural (BPHMF) resin, was prepared using a hydrolysis lignin (HL) as bio-phenol to partially substitute phenol and using glucose as a precursor for HMF. To enhance the chemical reactivity of the hydrolysis lignin with very high molecular weight, the HL was first degraded to de-polymerized hydrolysis lignin (DHL) followed by phenolation. BPHMF resin was then synthesized by resinification reaction between the phenolated DHL and HMF in-situ derived from glucose under pressure in the presence of Lewis acid catalysts, at an 85% yield. The resin was curable with 15 wt.% hexamethylenetetramine (HMTA) and the crosslinkage of the resin could also be strengthened by the functional groups in the DHL structure. Thermal/curing behaviors of the BPHMF-HMTA systems were studied using differential scanning calorimetry (DSC), peaking at 152 °C. The cured BPHMF resin demonstrated excellent thermal/thermomechanical properties, owing to the addition of HL, e.g., thermally stable up to 315 °C. The BPHMF-fiberglass thermoset composite demonstrated a high glass transition temperature (272 °C), and tensile strength (89 MPa) comparable to other phenolic composites.
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