Institute of Chemistry and Chemical Technology, Krasnoyarsk Science Center, Siberian Branch, Russian Academy of Sciences, Akademgorodok 50/24, 660036 Krasnoyarsk, Russia.
School of Non-Ferrous Metals and Material Science, Siberian Federal University, Pr. Svobodny 79, 660041 Krasnoyarsk, Russia.
Molecules. 2022 Sep 26;27(19):6356. doi: 10.3390/molecules27196356.
For the first time, the process of birch ethanol lignin sulfation with a sulfamic acid-urea mixture in a 1,4-dioxane medium was optimized experimentally and numerically. The high yield of the sulfated ethanol lignin (more than 96%) and containing 7.1 and 7.9 wt % of sulfur was produced at process temperatures of 80 and 90 °C for 3 h. The sample with the highest sulfur content (8.1 wt %) was obtained at a temperature of 100 °C for 2 h. The structure and molecular weight distribution of the sulfated birch ethanol lignin was established by FTIR, 2D H and C NMR spectroscopy, and gel permeation chromatography. The introduction of sulfate groups into the lignin structure was confirmed by FTIR by the appearance of absorption bands characteristic of the vibrations of sulfate group bonds. According to 2D NMR spectroscopy data, both the alcohol and phenolic hydroxyl groups of the ethanol lignin were subjected to sulfation. The sulfated birch ethanol lignin with a weight average molecular weight of 7.6 kDa and a polydispersity index of 1.81 was obtained under the optimum process conditions. Differences in the structure of the phenylpropane units of birch ethanol lignin (syringyl-type predominates) and abies ethanol lignin (guaiacyl-type predominates) was manifested in the fact that the sulfation of the former proceeds more completely at moderate temperatures than the latter. In contrast to sulfated abies ethanol lignin, the sulfated birch ethanol lignin had a bimodal and wider molecular weight distribution, as well as less thermal stability. The introduction of sulfate groups into ethanol lignin reduced its thermal stability.
首次在 1,4-二氧六环介质中使用硫酸氨基脲混合物对桦木乙醇木质素进行磺化,从实验和数值两方面对该过程进行了优化。在 80 和 90°C 下反应 3 小时,可得到产率高于 96%、含硫量为 7.1 和 7.9wt%的磺化乙醇木质素。在 100°C 下反应 2 小时,可得到含硫量最高(8.1wt%)的样品。通过傅里叶变换红外光谱(FTIR)、二维 H 和 C NMR 光谱以及凝胶渗透色谱(GPC)确定了磺化桦木乙醇木质素的结构和分子量分布。通过 FTIR 可以看出,木质素结构中引入了硫酸盐基团,出现了特征硫酸盐基团键振动的吸收带。根据二维 NMR 光谱数据,乙醇木质素中的醇羟基和酚羟基都发生了磺化。在最佳工艺条件下,得到重均分子量为 7.6 kDa、多分散指数为 1.81 的磺化桦木乙醇木质素。桦木乙醇木质素(以愈创木基型为主)和云杉乙醇木质素(以紫丁香基型为主)中苯丙烷单元结构的差异表现为,前者在中等温度下的磺化反应比后者更完全。与磺化云杉乙醇木质素不同,磺化桦木乙醇木质素有更宽的双峰分子量分布和更低的热稳定性。硫酸盐基团的引入降低了乙醇木质素的热稳定性。