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通过芬顿试剂氧化交联制备高强度、疏水性能的淀粉基粘合剂。

Preparation of a high-strength, hydrophobic performance starch-based adhesive with oxidative cross-linking via Fenton's reagent.

作者信息

Liu Mengyao, Yao Wenrui, Zheng Hao, Zhao Hangqi, Shao Ruoxi, Tan Haiyan, Zhang Yanhua

机构信息

Key Laboratory of Bio-based Material Science & Technology (Northeast Forestry University), Ministry of Education, Harbin 150040, China; Engineering Research Center of Advanced Wooden Materials (Northeast Forestry University), Ministry of Education, Harbin 150040, China.

Key Laboratory of Bio-based Material Science & Technology (Northeast Forestry University), Ministry of Education, Harbin 150040, China; Engineering Research Center of Advanced Wooden Materials (Northeast Forestry University), Ministry of Education, Harbin 150040, China.

出版信息

Int J Biol Macromol. 2023 Dec 31;253(Pt 5):126995. doi: 10.1016/j.ijbiomac.2023.126995. Epub 2023 Oct 4.

Abstract

Starch is a highly attractive carbohydrate in the production for the preparation of adhesives in recent years, due to its widespread availability, renewability, and abundance of reactive hydroxyl groups. However, the mechanical properties, hydrophobicity, self-adhesion, and particularly high energy efficiency are generally unsatisfactory for current starch-based adhesives. On this premise, starch was oxidized using Fenton's reagent in a ""one-pot cooking" process. The prepared oxidized starch was chain expanded by polyvinyl alcohol (PVA) and then cross-linked with a 10 % isocyanate (PM-200) to fabricate a starch-based adhesive (SFA) with a network crosslinked structure. SFA/2.5-55 adhesive shows significantly higher wet shear strength (1.18 MPa), a remarkable 94 % increase compared to SFA/2.5-55. The adhesive film also demonstrates both hydrophobicity (99° contact angle) and exceptional energy efficiency, with a DSC test revealing a notable 10 % elevation in energy efficiency. In addition, the crosslinked structure increases its molecular weight, thereby increasing its self-adhesion (Fig. S1). This study opens up new possibilities for the design and manufacture of multifunctional starch-based adhesives.

摘要

近年来,由于淀粉广泛可得、可再生且含有大量活性羟基,它在制备粘合剂的生产中是一种极具吸引力的碳水化合物。然而,目前淀粉基粘合剂的机械性能、疏水性、自粘性,尤其是能源效率普遍不尽人意。在此前提下,淀粉在“一锅煮”过程中用芬顿试剂进行氧化。制备的氧化淀粉通过聚乙烯醇(PVA)进行扩链,然后与10%的异氰酸酯(PM - 200)交联,以制备具有网络交联结构的淀粉基粘合剂(SFA)。SFA/2.5 - 55粘合剂表现出显著更高的湿剪切强度(1.18MPa),与SFA/2.5 - 55相比显著提高了94%。该粘合剂膜还兼具疏水性(99°接触角)和卓越的能源效率,差示扫描量热法(DSC)测试显示能源效率显著提高了10%。此外,交联结构增加了其分子量,从而提高了其自粘性(图S1)。本研究为多功能淀粉基粘合剂的设计和制造开辟了新的可能性。

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