Biomaterials Chemistry, Faculty of Forestry, University of British Columbia, Vancouver, BC, Canada.
Biomacromolecules. 2010 Apr 12;11(4):981-8. doi: 10.1021/bm901455p.
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.
采用原子转移自由基聚合(ATRP),利用选择性修饰的木质素基大分子引发剂,实现了 N-异丙基丙烯酰胺(NIPAM)与阔叶木硫酸盐木质素(HWKL)的共聚。通过改变 DMF/水溶剂体系的比例从 5:0 至 0:5,聚 NIPAM 接枝侧链的聚合度(DP)受到影响,当比例为 1:4(v/v)时,得到了估计 DP(NIPAM)>40 的结果。木质素-g-聚 NIPAM 共聚物的热分解温度随 DP(NIPAM)的增加而显著升高。同样,木质素-g-聚 NIPAM 共聚物在水中的溶解度取决于共聚物结构。在水溶性和悬浮共聚物中,在 32 摄氏度以上的温度下,g-聚 NIPAM 组分经历了典型的亲水-疏水转变,导致共聚物沉淀。