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Study of The Reaction Mechanism to Produce Nanocellulose-Graft-Chitosan Polymer

机译:制备纳米纤维素接枝壳聚糖聚合物的反应机理研究

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摘要

Cellulose and chitin are the most abundant polymeric materials in nature, capable of replacing conventional synthetic polymers. From them, cellulose nano/microfibers (CNFs/CMFs) and chitosan are obtained. Both polymers have been used separately in graft copolymerization but there are not many studies on the use of cellulose and chitosan together as copolymers and the reaction mechanism is unknown. In this work, the reaction mechanism to produce nano/microcellulose-graft-chitosan polymer has been studied. Recycled cellulose pulp was used, with and without a 2,2,6,6-tetramethylpiperidin-1-oxyl-radical (TEMPO)-mediated oxidation pretreatment, to produce CNFs and CMFs, respectively. For chitosan, a low-molecular weight product dissolved in an acetic acid solution was prepared. Grafted polymers were synthesized using a microwave digester. Results showed that TEMPO-mediated oxidation as the cellulose pretreatment is a key factor to obtain the grafted polymer CNF-g-CH. A reaction mechanism has been proposed where the amino group of chitosan attacks the carboxylic group of oxidized cellulose, since non-oxidized CMFs do not achieve the desired grafting. 13C NMR spectra, elemental analysis and SEM images validated the proposed mechanism. Finally, CNF-g-CH was used as a promising material to remove water-based inks and dyes from wastewater.
机译:纤维素和几丁质是自然界中最丰富的聚合材料,能够代替传统的合成聚合物。从它们中获得纤维素纳米/微纤维(CNFs / CMFs)和壳聚糖。两种聚合物已分别用于接枝共聚,但是关于将纤维素和壳聚糖一起用作共聚物的研究很少,反应机理尚不清楚。在这项工作中,已经研究了制备纳米/微纤维素接枝壳聚糖聚合物的反应机理。使用再生纤维素纸浆,分别在有和没有2,2,6,6-四甲基哌啶-1-氧基-自由基(TEMPO)介导的氧化预处理中进行生产,分别生产CNF和CMF。对于壳聚糖,制备了溶解在乙酸溶液中的低分子量产物。使用微波蒸煮器合成了接枝的聚合物。结果表明,TEMPO介导的氧化作为纤维素的预处理是获得接枝聚合物CNF-g-CH的关键因素。已经提出了一种反应机理,其中壳聚糖的氨基攻击氧化的纤维素的羧基,因为未氧化的CMF不能实现所需的接枝。 13 C NMR光谱,元素分析和SEM图像验证了该机理。最后,CNF-g-CH被用作从废水中去除水性油墨和染料的有前途的材料。

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