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用于改善TEMPO-CNCs表面疏水性和热稳定性的TEMPO氧化纤维素中羧基的酰胺化反应。

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

作者信息

Yoshikawa Yuki, Yamato Kyohei, Ishida Akiko, Yoshida Yutaka, Kumamoto Yoshiaki, Isogai Akira

机构信息

R&D Performance Chemicals Research, Kao Corporation, 1334 Minato, Wakayama 640-8580, Japan.

R&D Analytical Science Research, Kao Corporation, 1334 Minato, Wakayama 640-8580, Japan.

出版信息

Carbohydr Polym. 2025 Jan 1;347:122654. doi: 10.1016/j.carbpol.2024.122654. Epub 2024 Aug 23.

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-NH 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.

摘要

制备具有高机械强度、光学透明度和热稳定性的各种材料(如环氧纳米复合材料)需要具有高热降解点的表面疏水化纤维素纳米材料(CNs)。对含有大量羧基的亲水性CNs进行酰胺化是一种可能的化学改性方法。然而,在工业应用中,要实现CNs中高比例羧基的高效酰胺化极具挑战性。在本研究中,含羧基的纤维木浆在非均相固/液体系中进行酰胺化,以制备具有高酰胺化率和高收率的产品,同时实施经济高效的分离和纯化工艺。因此,首先制备了具有大量羧基的部分酸水解木浆。随后,分别使用聚亚烷基二醇-NH和辛胺成功地将木浆中88%和91%的羧基进行了酰胺化。这是通过分别使用4-(4,6-二甲氧基-1,3,5-三嗪-2-基)-4-甲基吗啉鎓氯化物和N-甲基吗啉作为缩合剂和活化剂,在约23°C的N,N-二甲基甲酰胺(DMF)中反应16小时来实现的。酰胺化后,热降解点从酸水解木浆的224°C提高到超过250°C。然后,通过在环氧单体/DMF混合物中使用高压均质化将酰胺化木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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