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功能化二氧化硅纳米粒子改性环氧结构胶粘剂的冲击楔-剥离性能比较研究

Comparative Study of the Impact Wedge-Peel Performance of Epoxy Structural Adhesives Modified with Functionalized Silica Nanoparticles.

作者信息

Chae Gyeong-Seok, Park Hee-Woong, Kwon Kiok, Shin Seunghan

机构信息

Green Chemistry & Materials Group, Korea Institute of Industrial Technology (KITECH), Cheonan, Chungnam 31056, Korea.

Department of Green Process and System Engineering, University of Science & Technology (UST), Daejeon, Chungnam 34113, Korea.

出版信息

Polymers (Basel). 2021 Feb 2;13(3):469. doi: 10.3390/polym13030469.

Abstract

Epoxy structural adhesives have strong adhesion, minimal shrinkage and high thermal and chemical resistance. However, despite these excellent properties, their high-energy impact resistance should be improved to satisfy the increasing demands of the automotive industry. For this reason, we used four types of silica nanoparticles with different surface groups, such as polydimethylsiloxane (PDMS), hydroxyl, epoxy and amine groups, as toughening agents and examined their effect on the glass transition temperature (), crosslinking density and phase separation of epoxy structural adhesives. High-energy impact resistance, mode I fracture toughness and lap shear strength were also measured to explain the effect of surface functional groups. Silica nanoparticles with reactive functional groups increased the mode I fracture toughness of epoxy structural adhesives without sacrificing the crosslinking density. Although the mode I fracture toughness of epoxy structural adhesives could not clearly show the effect of surface functional groups, the dynamic resistance to cleavage obtained by impact wedge-peel tests showed quite different values. At a 0.3 vol% content, epoxy-functionalized silica nanoparticles induced the highest value (40.2 N/mm) compared to PDMS (34.1 N/m), hydroxyl (34.9 N/mm), and amine (36.1 N/m). All of these values were significantly higher than those of pristine epoxy structural adhesive (27.7 N/mm).

摘要

环氧结构胶粘剂具有很强的附着力、最小的收缩率以及高耐热性和耐化学性。然而,尽管具有这些优异性能,但其抗高能冲击性仍需提高,以满足汽车行业日益增长的需求。因此,我们使用了四种具有不同表面基团的二氧化硅纳米颗粒,如聚二甲基硅氧烷(PDMS)、羟基、环氧基和胺基,作为增韧剂,并研究了它们对环氧结构胶粘剂的玻璃化转变温度、交联密度和相分离的影响。还测量了抗高能冲击性、I型断裂韧性和搭接剪切强度,以解释表面官能团的作用。具有反应性官能团的二氧化硅纳米颗粒在不牺牲交联密度的情况下提高了环氧结构胶粘剂的I型断裂韧性。尽管环氧结构胶粘剂的I型断裂韧性不能清楚地显示表面官能团的作用,但通过冲击楔形剥离试验获得的动态抗劈裂性显示出相当不同的值。在0.3体积%的含量下,与PDMS(34.1 N/mm)、羟基(34.9 N/mm)和胺基(36.1 N/mm)相比,环氧官能化二氧化硅纳米颗粒诱导出最高值(40.2 N/mm)。所有这些值均显著高于原始环氧结构胶粘剂的值(27.7 N/mm)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0266/7867298/30ceb5d82a52/polymers-13-00469-g001.jpg

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