木质素
软木
溶剂分解
硫酸
聚乙二醇
材料科学
PEG比率
化学工程
极限抗拉强度
纤维素
碳化
硬木
有机化学
复合材料
化学
水解
扫描电子显微镜
生态学
财务
经济
生物
工程类
作者
Jian Lin,Satoshi Kubo,Takatoshi Yamada,Keiichi Koda,Yasumitsu Uraki
出处
期刊:Bioresources
[North Carolina State University]
日期:2012-10-05
卷期号:7 (4)
被引量:28
标识
DOI:10.15376/biores.7.4.5634-5646
摘要
A thermally fusible softwood lignin was directly isolated by a solvolysis of cedar wood chips with a mixture of polyethylene glycol 400 (PEG 400) and sulfuric acid. Its fusibility was found to be due to a PEG moiety introduced into the lignin by the solvolysis. The lignin was easily formed into fibers by melt-spinning at temperatures ranging from 145 to 172 °C without any modification. The lignin fibers could be converted into infusible fibers as a precursor for carbon fibers (CFs) by conventional oxidative thermal stabilization processing in air or a stream of oxygen for 2 days. We found that the infusible fibers resulted from the partial cleavage of the PEG moiety from the lignin fibers after treatment with 6 M hydrochloric acid at 100 °C for 2 h. The infusible fibers were converted into CFs with a tensile strength of 450 MPa by carbonization at 1000 °C under a N2 stream.
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