Amidation of carboxy groups in TEMPO-oxidized cellulose for improving surface hydrophobization and thermal stability of TEMPO-CNCs

IF 10.7 1区 化学 Q1 CHEMISTRY, APPLIED
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Abstract

Surface-hydrophobized cellulose nanomaterials (CNs) with high thermal degradation points are required for preparing various materials, such as epoxy nanocomposites, which possess high mechanical strength, optical transparency, and thermal stability. Amidation of carboxy groups in CNs is one possible chemical modification for hydrophilic CNs that contain abundant carboxy groups. However, achieving efficient amidation of high ratios of carboxy groups in CNs is highly challenging for industrial applications. In this study, carboxy group-containing fibrous wood pulp was subjected to amidation in heterogeneous solid/liquid systems to prepare products with high amidation ratios and high yields, while implementing cost-effective isolation and purification processes. Consequently, a partially acid-hydrolyzed wood pulp with abundant carboxy groups was first prepared. Subsequently, 88 % and 91 % of the carboxy groups in the pulp were successfully amidated using polyalkylene glycols-NH2 and octylamine, respectively. This was achieved by utilizing 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride and N-methylmorpholine as the condensation reagent and activator, respectively, in N,N-dimethylformamide (DMF) at approximately 23 °C for 16 h. The thermal degradation point increased from 224 °C for the acid-hydrolyzed pulp to over 250 °C after amidation. The amidated pulps were then converted into transparent dispersions, consisting of amidated cellulose nanocrystals, by homogenization in an epoxy monomer/DMF mixture using high-pressure homogenization.

Abstract Image

氨化 TEMPO 氧化纤维素中的羧基以改善 TEMPO-CNC 的表面疏水性和热稳定性
制备具有高机械强度、光学透明度和热稳定性的环氧纳米复合材料等各种材料时,需要具有高热降解点的表面疏水性纤维素纳米材料(CN)。对于含有大量羧基的亲水性氯化萘来说,酰胺化氯化萘中的羧基是一种可行的化学改性方法。然而,实现氯化萘中高比例羧基的高效酰胺化对于工业应用而言极具挑战性。在本研究中,含羧基的纤维木浆在异构固/液体系中进行酰胺化,以制备高酰胺化比率和高产率的产品,同时采用具有成本效益的分离和纯化工艺。因此,首先制备出了含有大量羧基的部分酸水解木浆。随后,使用聚亚烷基二醇-NH2 和辛胺分别成功地酰胺化了纸浆中 88% 和 91% 的羧基。在 N,N-二甲基甲酰胺(DMF)中,以 4-(4,6-二甲氧基-1,3,5-三嗪-2-基)-4-甲基吗啉氯化物和 N-甲基吗啉分别作为缩合试剂和活化剂,在约 23 °C、16 小时的条件下进行。然后,在环氧单体/DMF 混合物中使用高压匀浆法将酰胺化纸浆转化为由酰胺化纤维素纳米晶体组成的透明分散体。
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来源期刊
Carbohydrate Polymers
Carbohydrate Polymers 化学-高分子科学
CiteScore
22.40
自引率
8.00%
发文量
1286
审稿时长
47 days
期刊介绍: Carbohydrate Polymers stands as a prominent journal in the glycoscience field, dedicated to exploring and harnessing the potential of polysaccharides with applications spanning bioenergy, bioplastics, biomaterials, biorefining, chemistry, drug delivery, food, health, nanotechnology, packaging, paper, pharmaceuticals, medicine, oil recovery, textiles, tissue engineering, wood, and various aspects of glycoscience. The journal emphasizes the central role of well-characterized carbohydrate polymers, highlighting their significance as the primary focus rather than a peripheral topic. Each paper must prominently feature at least one named carbohydrate polymer, evident in both citation and title, with a commitment to innovative research that advances scientific knowledge.
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