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硅烷偶联剂化学性质对再生碳纤维表面处理中与热塑性塑料界面结合强度的影响

Effect of the Chemical Properties of Silane Coupling Agents on Interfacial Bonding Strength with Thermoplastics in the Resizing of Recycled Carbon Fibers.

作者信息

Lee Hyunkyung, Kim Minsu, Kim Gyungha, Kim Daeup

机构信息

Carbon & Light Materials Application Group, Korea Institute of Industrial Technology, Bucheon 14449, Republic of Korea.

Department of Carbon Material Fiber Engineering, Chonbuk National University, Jeonju 54896, Republic of Korea.

出版信息

Polymers (Basel). 2023 Oct 30;15(21):4273. doi: 10.3390/polym15214273.

Abstract

Upcycling recycled carbon fibers recovered from waste carbon composites can reduce the price of carbon fibers while improving disposal-related environmental problems. This study assessed and characterized recycled carbon fibers subjected to sizing treatment using N-(2-aminoethyl)-3-aminopropyltrimethoxysilane (APS) chemically coordinated with polyamide 6 (PA6) and polypropylene (PP) resins. Sizing treatment with 1 wt.% APS for 10 s yielded O=C-O on the surface of the carbon fiber, and the -SiOH in the APS underwent a dehydration-condensation reaction that converted O=C-O (lactone groups) into bonds of C-O (hydroxyl groups) and C=O (carbonyl groups). The effects of C-O and C=O on the interfacial bonding force increased to a maximum, resulting in an oxygen-to-carbon ratio (O/C) of 0.26. The polar/surface energy ratio showed the highest value of 32.29% at 10 s, and the interfacial bonding force showed the maximum value of 32 MPa at 10 s, which is about 15% better than that of commercial carbon fiber (PA6-based condition). In 10 s resizing treatments with 0.5 wt.% 3-methacryloxypropyltrimethoxysilane (MPS), C-O, C=O, and O=C-O underwent a dehydration-condensation reaction with -SiOH, which broke the bonds between carbon and oxygen and introduced a methacrylate group (H2C=C(CH)COH), resulting in a significant increase in C-O and C=O, with an O/C of 0.51. The polar/surface free energy ratio was about 38% at 10 s, with the interfacial bonding force increasing to 27% compared to commercial carbon fiber (PP-based conditions). MPS exhibited a superior interfacial shear strength improvement, two times higher than that of APS, with excellent coordination with PP resin and commercial carbon fiber, although the interfacial bonding strength of the PP resin was significantly lower.

摘要

对从废弃碳复合材料中回收的再生碳纤维进行升级改造,既能降低碳纤维价格,又能改善与废弃物处理相关的环境问题。本研究对使用N-(2-氨乙基)-3-氨丙基三甲氧基硅烷(APS)进行上浆处理的再生碳纤维进行了评估和表征,APS与聚酰胺6(PA6)和聚丙烯(PP)树脂发生化学配位。用1 wt.%的APS进行10秒的上浆处理后,碳纤维表面产生了O=C-O,APS中的-SiOH发生脱水缩合反应,将O=C-O(内酯基团)转化为C-O(羟基)和C=O(羰基)的键。C-O和C=O对界面结合力的影响增大到最大值,导致氧碳比(O/C)为0.26。极性/表面能比在10秒时显示出最高值32.29%,界面结合力在10秒时显示出最大值32 MPa,比商业碳纤维(基于PA6的条件)约高15%。在用0.5 wt.%的3-甲基丙烯酰氧基丙基三甲氧基硅烷(MPS)进行10秒的上浆处理中,C-O、C=O和O=C-O与-SiOH发生脱水缩合反应,打破了碳和氧之间的键,并引入了甲基丙烯酸酯基团(H2C=C(CH)COH),导致C-O和C=O显著增加,O/C为0.51。极性/表面自由能比在10秒时约为38%,与商业碳纤维(基于PP的条件)相比,界面结合力提高了27%。MPS表现出优异的界面剪切强度提升效果,比APS高两倍,与PP树脂和商业碳纤维具有良好的配位性,尽管PP树脂的界面结合强度明显较低。

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