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通过湿纺,将植物纤维不均匀乙酰化为微纳米纤维素,用于合成具有高拉伸性、韧性和耐水性的共连续长丝。

Heterogeneous Acetylation of Plant Fibers into Micro- and Nanocelluloses for the Synthesis of Highly Stretchable, Tough, and Water-Resistant Co-continuous Filaments via Wet-Spinning.

机构信息

Department of Chemical & Biomolecular Engineering , NC State University , Raleigh , North Carolina 27695-7905 , United States.

Department of Forest Biomaterials , NC State University , Raleigh , North Carolina 27695-8001 , United States .

出版信息

ACS Appl Mater Interfaces. 2018 Dec 26;10(51):44776-44786. doi: 10.1021/acsami.8b17790. Epub 2018 Dec 11.

Abstract

Heterogeneous acetylation of wood fibers is proposed for weakening their interfibrillar hydrogen bonding, which facilitates their processing into micro- and nanocelluloses that can be further used to synthesize filaments via wet-spinning. The structural (SEM, WAXD), molecular (SEC), and chemical (FTIR, titration) properties of the system are used to propose the associated reaction mechanism. Unlike the homogeneous acetylation, this method does not alter the main morphological features of cellulose fibrils. Thus, we show for the first time, the exploitation of synergies of compositions simultaneously comprising dissolved cellulose esters and suspended cellulose micro- and nanofibrils. Such colloidal suspension forms a co-continuous assembly with a matrix that interacts strongly with the micro- and nanofibrils in the dispersed phase. This facilitates uninterrupted and defect-free wet-spinning. Upon contact with an antisolvent (water), filaments are easily formed and display a set of properties that set them apart from those reported so far for nanocelluloses: a remarkable stretchability (30% strain) and ultrahigh toughness (33 MJ/m), both surpassing the values of all reported nanocellulose-based filaments. All the while, they also exhibit competitive stiffness and strength (6 GPa and 143 MPa, respectively). Most remarkably, they retain 90% of these properties after long-term immersion in water, solving the main challenge of the lack of wet strength that is otherwise observed for filaments synthesized from nanocelluloses.

摘要

提出了对木纤维进行不均匀乙酰化,以削弱其纤维间氢键,从而便于将其加工成微纳米纤维素,进一步通过湿法纺丝合成纤维。利用系统的结构(SEM、WAXD)、分子(SEC)和化学特性(FTIR、滴定)来提出相关的反应机制。与均相乙酰化不同,该方法不会改变纤维素纤维的主要形态特征。因此,我们首次展示了同时包含溶解纤维素酯和悬浮纤维素微纳米纤维的协同作用的利用。这种胶体悬浮液与基质形成共连续组装,与分散相中的微纳米纤维强烈相互作用。这便于无中断和无缺陷的湿法纺丝。与非溶剂(水)接触时,很容易形成纤维,并显示出一组与迄今为止报道的纳米纤维素不同的性质:显著的拉伸性(30%应变)和超高韧性(33MJ/m),均超过所有报道的基于纳米纤维素纤维的数值。同时,它们还表现出具有竞争力的刚度和强度(分别为 6GPa 和 143MPa)。最显著的是,它们在水中长期浸泡后仍保留 90%的这些特性,解决了由纳米纤维素合成纤维所观察到的缺乏湿强度的主要挑战。

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