共聚物
原子转移自由基聚合
高分子化学
木质素
聚合
化学
溶解度
溶剂
聚合物
自由基聚合
化学工程
有机化学
工程类
作者
Yong Sik Kim,John F. Kadla
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2010-02-26
卷期号:11 (4): 981-988
被引量:184
摘要
Copolymerization of N-isopropylacrylamide (NIPAM) with technical hardwood kraft lignin (HWKL) was achieved by atom transfer radical polymerization (ATRP) using a selectively modified lignin-based macroinitiator. The degree of polymerization (DP) of polyNIPAM graft side chains was affected by varying the ratio of the DMF/water solvent system from 5:0 to 0:5, and an estimated DP(NIPAM) of >40 was obtained using a ratio of 1:4 (v/v). The thermal decomposition temperature of the lignin-g-polyNIPAM copolymers significantly increased with increasing DP(NIPAM). Likewise, the solubility of the lignin-g-polyNIPAM copolymers in water changed depending on copolymer structure. In both the water-soluble and suspended copolymers, at temperatures above 32 degrees C, the g-polyNIPAM component underwent the typical hydrophilic-to-hydrophobic transition, resulting in the precipitation of the copolymer.
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