Hua Qi, Liu Li-Yang, Karaaslan Muzaffer A, Renneckar Scott
Department of Wood Science, The University of British Columbia, Vancouver, BC, Canada.
Front Chem. 2019 Jul 18;7:515. doi: 10.3389/fchem.2019.00515. eCollection 2019.
An aqueous biopolymer dispersion coating system was synthesized utilizing softwood kraft lignin and a long chain organic acid. The chemical treatment of lignin was a two-step procedure, which first consisted of hydroxyethylation of the phenolic groups on lignin utilizing ethylene carbonate and an alkaline catalyst. This first step resulted in the lignin containing more than 80% aliphatic hydroxyl functionality (H NMR). Following this step, oleic acid was reacted with hydoxyethyl lignin in order to form ester derivatives. With nearly a total reduction in absorbance in the hydroxyl stretching region, FT-IR analysis showed the majority of the hydroxyl groups was esterified forming an ethyl oleate derivative. Semi-quantitative C NMR analysis of the lignin revealed 88% substitution of the lignin hydroxyl groups. This derivative was soluble in organic solvent such as toluene and tetrahydrofuran. Solutions of lignin derivatives were slowly precipitated through dialysis, resulting in a stable dispersion of lignin microparticles in distilled water. The 1-2 μm average diameter size of the precipitated particles was found with dynamic light scattering of the suspensions. Spray and spin coating were used to apply the lignin derivative dispersion to different surfaces. For both coating methods, the lignin-based particles enhanced the hydrophobicity of all the substrates tested, resulting in increased water contact angles for glass, kraft pulp sheets and solid wood. Benign reagents involved in the coating synthesis utilized natural compounds that are known to repel water in nature. Combined with the avoidance of volatile organic solvents during application, this process provided a low environmental footprint solution for synthesis of hydrophobic coatings.
利用软木硫酸盐木质素和一种长链有机酸合成了一种水性生物聚合物分散体涂层体系。木质素的化学处理是一个两步过程,第一步是利用碳酸亚乙酯和碱性催化剂对木质素上的酚羟基进行羟乙基化反应。第一步反应后,木质素中含有超过80%的脂肪族羟基官能团(核磁共振氢谱)。在这一步之后,油酸与羟乙基木质素反应以形成酯衍生物。傅里叶变换红外光谱分析表明,在羟基伸缩振动区域吸光度几乎完全降低,这表明大多数羟基已被酯化形成油酸乙酯衍生物。木质素的半定量核磁共振碳谱分析表明,木质素羟基的取代率为88%。这种衍生物可溶于甲苯和四氢呋喃等有机溶剂。木质素衍生物溶液通过透析缓慢沉淀,从而在蒸馏水中形成稳定的木质素微粒分散体。通过对悬浮液进行动态光散射发现,沉淀颗粒的平均直径大小为1-2μm。采用喷涂和旋涂法将木质素衍生物分散体涂覆到不同表面上。对于这两种涂覆方法,木质素基颗粒均增强了所有测试基材的疏水性,导致玻璃、牛皮纸浆片和实木的水接触角增大。涂层合成过程中使用的良性试剂采用了自然界中已知的能防水的天然化合物。再加上在涂覆过程中避免使用挥发性有机溶剂,该工艺为合成疏水涂层提供了一种低环境影响的解决方案。