Yin Chongxin, Wang Min, Ma Qingzhi, Bian Huiyang, Ren Hao, Dai Hongqi, Cheng Jinlan
Jiangsu Co-Innovation Center for Efficient Processing and Utilization of Forest Resources, Jiangsu Provincial Key Lab of Pulp & Paper Science & Technology, Nanjing Forestry University, Nanjing 210037, China.
Zhejiang Provincial Collaborative Innovation Center of Agricultural Biological Resources Biochemical Manufacturing, Zhejiang University of Science and Technology, Hangzhou 310023, China.
Molecules. 2021 Jul 6;26(14):4123. doi: 10.3390/molecules26144123.
Rice straw hydrotropic lignin was extracted from -Toluene sulfonic acid (-TsOH) fractionation with a different combined delignification factor (CDF). Hydrotropic lignin characterization was systematically investigated, and alkaline lignin was also studied for the contrast. Results showed that the hydrotropic rice straw lignin particle was in nanometer scopes. Compared with alkaline lignin, the hydrotropic lignin had greater molecular weight. NMR analysis showed that β-aryl ether linkage was well preserved at low severities, and the unsaturation in the side chain of hydrotropic lignin was high. H units and G units were preferentially degraded and subsequently condensed at high severity. High severity also resulted in the cleavage of part β-aryl ether linkage. P-NMR showed the decrease in aliphatic hydroxyl groups and the increasing carboxyl group content at high severity. The maximum weight loss temperature of the hydrotropic lignin was in the range of 330-350 °C, higher than the alkaline lignin, and the glass conversion temperature (T) of the hydrotropic lignin was in the range of 107-125 °C, lower than that of the alkaline lignin. The hydrotropic lignin has high β-aryl ether linkage content, high activity, nanoscale particle size, and low T, which is beneficial for its further valorization.
采用不同的组合脱木质素因子(CDF)从对甲苯磺酸(-TsOH)分级中提取稻草向水性木质素。系统地研究了向水性木质素的特性,并以碱性木质素作为对比进行了研究。结果表明,向水性稻草木质素颗粒处于纳米尺度。与碱性木质素相比,向水性木质素具有更大的分子量。核磁共振分析表明,在低强度条件下β-芳基醚键得到了很好的保留,且向水性木质素侧链的不饱和度较高。在高强度条件下,H单元和G单元优先降解,随后发生缩合。高强度还导致部分β-芳基醚键断裂。磷核磁共振显示,在高强度条件下脂肪族羟基减少,羧基含量增加。向水性木质素的最大失重温度在330-350℃范围内,高于碱性木质素,且向水性木质素的玻璃化转变温度(Tg)在107-125℃范围内,低于碱性木质素。向水性木质素具有高β-芳基醚键含量、高活性、纳米级粒径和低Tg,这有利于其进一步增值利用。