首页> 美国卫生研究院文献>Materials >Study on the Dissolution Mechanism of Cellulose by ChCl-Based Deep Eutectic Solvents
【2h】

Study on the Dissolution Mechanism of Cellulose by ChCl-Based Deep Eutectic Solvents

机译:基于ChCl的深共晶溶剂对纤维素的溶解机理研究

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Four deep eutectic solvents (DESs), namely, glycerol/chlorocholine (glycerol/ChCl), urea/ChCl, citric acid/ChCl, and oxalic acid/ChCl, were synthesized and their performance in the dissolution of cellulose was studied. The results showed that the melting point of the DESs varied with the proportion of the hydrogen bond donor material. The viscosity of the DESs changed considerably with the change in temperature; as the temperature increased, the viscosity decreased and the electrical conductivity increased. Oxalic acid/ChCl exhibited the best dissolution effects on cellulose. The microscopic morphology of cellulose was observed with a microscope. The solvent system effectively dissolved the cellulose, and the dissolution method of the oxalic acid/ChCl solvent on cellulose was preliminarily analyzed. The ChCl solvent formed new hydrogen bonds with the hydroxyl groups of the cellulose through its oxygen atom in the hydroxyl group and its nitrogen atom in the amino group. That is to say, after the deep eutectic melt formed an internal hydrogen bond, a large number of remaining ions formed a hydrogen bond with the hydroxyl groups of the cellulose, resulting in a great dissolution of the cellulose. Although the cellulose and regenerated cellulose had similar structures, the crystal form of cellulose changed from type I to type II.
机译:合成了甘油/氯胆碱(甘油/ ChCl),尿素/ ChCl,柠檬酸/ ChCl和草酸/ ChCl四种深共晶溶剂(DESs),并研究了它们在纤维素溶解中的性能。结果表明,DES的熔点随氢键供体材料的比例而变化。 DES的粘度随温度的变化而变化很大。随着温度升高,粘度降低,电导率升高。草酸/ ChCl对纤维素的溶解效果最好。用显微镜观察纤维素的微观形态。该溶剂体系有效地溶解了纤维素,初步分析了草酸/ ChCl溶剂在纤维素上的溶解方法。 ChCl溶剂通过其羟基中的氧原子和氨基中的氮原子与纤维素的羟基形成新的氢键。也就是说,在深共晶熔体形成内部氢键之后,大量残留离子与纤维素的羟基形成氢键,导致纤维素的大量溶解。尽管纤维素和再生纤维素具有相似的结构,但是纤维素的晶体形式从I型变为II型。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号