共辐照接枝处理芳纶纤维F3A表面

以环氧氯丙烷为接枝剂,通过高能射线共辐照法对国产芳纶纤维(AFs)进行表面处理,对比了辐照前后芳纶表面形貌、动态接触角、表面自由能及其本体结晶情况变化。用不同辐照剂量下处理的纤维(IAFs-200和IAFs-400)制备了芳纶/环氧(IAFs/ER)复合材料,与未处理纤维相比,共辐照处理的芳纶增强复合材料的界面剪切强度(IFSS)和层间剪切强度(ILSS)分别提高了51.56%和25.79%。辐照处理后纤维表面活性的稳定性良好。     

表面处理对Kevlar纤维复合材料界面结合强度的影响

为改善芳纶纤维增强树脂基复合材料的界面结合强度,用化学处理法对Kevlar-29纤维进行表面处理,并用傅里叶变换红外光谱和扫描电镜等方法对表面接枝进行鉴定,用单丝拔出试验表征芳纶纤维增强树脂基复合材料的界面结合强度。实验结果表明,纤维经过表面改性后,在单丝断裂强度降低不大的情况下,界面剪切强度显著提高。     

Technora纤维的表面改性研究

采用不同浓度的2,4-甲苯二异氰酸酯（TDI）溶液对Technora纤维（芳纶）进行表面改性,对处理前后的样品进行了扫描电镜、单丝抗拉强度、界面抗剪切强度、红外和表面浸润性测试。结果表明该方法能在对纤维力学性能无损伤的情况下,有效的改善界面性能和表面浸润性。     

硅烷偶联剂对芳纶的优化改性

采用硅烷偶联剂KH-550对芳纶进行表面处理。通过单因素法分析硅烷偶联剂KH-550在不同处理条件(浓度、温度和时间)下芳纶的断裂强力和界面剪切强度;再通过正交实验法得到硅烷偶联剂KH-550改性芳纶的最佳方案。结果表明,硅烷偶联剂KH-550表面处理芳纶的最优工艺为:浓度20%,温度55℃,时间7 h;得到芳纶的界面剪切强度增加率远远高于断裂强力损失率,芳纶的断裂强力损失率为7.79%,界面剪切强度增加率为14.59%,有利于纤维与树脂界面的结合。     

环氧树脂/多巴胺增强芳纶纤维界面性能

由于芳纶纤维表面光滑且呈现化学惰性,与环氧树脂等基体材料结合后界面性能较差。为此,采用多巴胺在不同时间下对改进型芳纶Ⅲ纤维表面进行改性处理,并研究了对环氧树脂/多巴胺改性芳纶纤维界面性能的影响。对扫描电子显微镜对纤维改性前后表面形貌进行表征,发现纤维改性后表面粗糙度提高,利于与环氧树脂间界面结合。利用傅里叶变换红外光谱、X射线光电子能谱对纤维改性前后基团和表面元素含量进行表征,改性后纤维表面活性基团增加,极性增强。通过热重分析表明聚多巴胺成功吸附在纤维表面。测量纤维表面接触角,改性后的接触角更小,有利于环氧树脂润湿纤维。采用横向丝束复合材料的拉伸强度表征环氧树脂/芳纶纤维的界面性能。最终确定了多巴胺浓度为2 g/L,在多巴胺溶液中处理4 h为最佳条件,在该条件拉伸强度比为改性前提高了28.06%,拉伸弹性模量提高了14.68%。     

左旋多巴胺处理对芳纶表面结构与性能的影响

利用L-3,4-二羟基苯丙氨酸(L-DOPA)的氧化自聚合,在杂环芳纶表面修饰聚L-3,4-二羟基苯丙氨酸(PDOPA)活性涂层来提高芳纶的表面活性及耐紫外辐照性能。结果表明:改性后芳纶表面粗糙度显著提高,同时,PDOPA涂层上大量的羧基、羟基等活性单元均有利于增强与环氧树脂的机械锁合力,改性后芳纶/环氧树脂复合材料的界面剪切强度提高了32.0%。此外,上述改性过程对杂环芳纶本身力学性能影响较小,纤维的拉伸强度保持率可以达到100%,基本实现了无损改性。同时,由于PDOPA的保护作用,改性后芳纶的耐紫外辐射性能显著提高;经过168 h紫外线辐照处理后,其拉伸强度保持率可达到92.5%,显著提升了杂环芳纶的耐紫外线辐照特性。     

芳纶纤维等离子体接枝改性处理研究

采用等离子体接枝对芳纶纤维表面进行改性处理,采用XPS、浸润性、界面剪切强度对等离子体接枝处理前后的表面组成、复合材料界面粘接性能等进行了研究,结果表明:等离子体接枝处理可以有效地提高芳纶纤维表面的极性官能团,增加与基体树脂-环氧树脂的浸润性,进而提高芳纶/环氧复合材料的界面粘接强度.     

芳纶纤维/环氧树脂预浸料界面相容性的方法探究

预浸料要求树脂基体和增强纤维具有良好的匹配性,为了提高芳纶纤维/环氧树脂预浸料的界面相容性,本文从芳纶纤维表面改性及增韧技术两个方面进行综述,讨论了芳纶纤维物理改性和化学改性方法的优缺点,分析了界面增韧及环氧树脂基体的不同增韧途径,重点介绍了聚氨酯/环氧树脂互穿网络体系.认为芳纶纤维的偶联剂表面处理和聚氨酯增韧环氧树脂相结合,是提高芳纶纤维/环氧树脂预浸料层间剪切强度的的可行途径.     

芳纶表面改性研究进展

简单回顾了芳纶的发展历史,阐述了表面涂层法、化学改性、物理改性等几种芳纶表面改性方法的研究现状,同时介绍了3种常用来表征纤维复合材料界面结合强度的方法,最后指出芳纶表面改性技术的发展方向。     

γ射线辐照处理对芳纶纤维F-3A结构和性能的影响

为采用γ射线对芳纶纤维进行辐照处理,研究辐照对纤维表面形貌、拉伸性能、比浓黏度,表面能以及芳纶纤维复合材料机械性能的影响。实验结果显示,经过辐照处理后,纤维表面粗糙度,纤维的拉伸强度和比浓黏度发生明显变化,纤维在溶液中的浸润性能提高,表面能增大。当辐照强度为600k Gy时,纤维增强环氧树脂的层间剪切强度达到51.86MPa,提高了23.09%。     

Surface modification of aramid fibers with γ‐ray radiation for improving interfacial bonding strength with epoxy resin

Co⁶⁰ γ‐ray radiation as a simple and convenient method for surface modification of Armos aramid fibers was introduced in this article. Two kinds of gas mediums, N₂ and air, were chosen to modify aramid fiber surface by γ‐ray irradiation. After fiber surface treatment, the interlaminar shear strength values of aramid/epoxy composites were enhanced by about 17.7 and 15.8%, respectively. Surface elements of aramid fibers were determined by XPS, the analysis of which showed that the ratio of oxygen/carbon was increased. The crystalline state of aramid fibers was determined by X‐ray diffraction instrument. The surface topography of fibers was analyzed by atomic force microscopy and scanning electron microscope. The degree of surface roughness and the wettability of fiber surface were both enhanced by γ‐ray radiation. The results indicated that γ‐ray irradiation technique, which is a suitable way of batch process for industrialization, can significantly improve the surface properties of aramid fibers reinforced epoxy resin matrix composites. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Effect of ultrasound on wettability between aramid fibers and epoxy resin

Good wetting of reinforced fiber by resin was a main factor in the improvement of the interface adhesion of their composites. Ultrasound with a frequency of 20 kHz was used to improve the wettability between aramid fibers and epoxy resin during the winding process of the composites. The effects of ultrasound on the viscosity and surface tension of epoxy resin and on the surface characteristics of aramid fibers were investigated. The wettability of aramid fibers and treated epoxy resin under different conditions and of aramid fibers and epoxy resin under ultrasonic online treatment were compared. The results indicated that the main action of ultrasound was to force epoxy resin to impregnate aramid fibers, in addition to the influence of ultrasound on the properties of epoxy resin and aramid fibers. The results of microdebond testing showed that the interfacial shear strength (IFSS) of aramid/epoxy composites could be 26% higher than that of untreated composites because of the improved wettability between aramid fibers and epoxy resin subjected to ultrasonic online treatment. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci, 2006     

RETRACTED ARTICLE: Surface modification of aramid fibers with novel chemical approach

Friedel–Crafts Reaction as a simple and convenient approach to the surface modification of aramid fiber was introduced in this paper. Epoxy chloropropane was chosen as the treatment reagent to modify aramid fibers surface via Graft reaction. After the modification, the interfacial properties of aramid/epoxy composites were investigated by the single fiber pull-out test (SFP), and the mechanical properties of aramid fibers were investigated by the tensile strength test. The results showed that the interfacial shear strength (IFSS) value of aramid/epoxy composites was enhanced by about 50%, and the tensile strength of aramid fibers had no obvious damage. The crystalline state of aramid fibers was determined by X-ray diffraction instrument (XRD), and the results showed that there were not any distinct crystal type varieties. The surface elements of aramid fibers were determined by X-ray photoelectron spectroscopy (XPS), the analysis of which showed that the oxygen/carbon ratio of aramid fiber surface increased obviously. The possible changes of the chemical structure of aramid fibers were investigated via Fourier transform infrared spectrum (FTIR), and the analysis of which showed that the epoxy functional groups were grafted into the molecule structure of aramid fibers. The surface morphology of aramid fibers was analyzed by Scanning electron microscope (SEM), and the SEM results showed that the physical structure of aramid fibers was not etched or damaged obviously. The surface energy of aramid fibers was investigated via the dynamic capillary method, and the results showed that the surface energy was enhanced by 31.5%, and then the wettability degree of aramid fiber surface was enhanced obviously too. All of the results indicated that this novel chemical modification approach not only can improve the interfacial bonding strength of aramid/epoxy composites remarkably, but also have no negative influence on the intrinsic tensile strength of aramid fibers.     

氧化锌纳米棒阵列对芳纶的改性

利用湿化学方法在芳纶Ⅲ表面预制氧化锌(ZnO)晶种层,再在晶种膜的基础上制备出了垂直生长的ZnO纳米棒阵列。采用X射线衍射(XRD)、场发射扫描电镜(FE-SEM)和微脱黏试验对纤维表面的组成、形貌及复合材料的界面黏结性能进行了研究。结果表明:纤维表面生长的ZnO纳米棒阵列属于六方纤锌矿晶相,纳米棒垂直生长在纤维表面,增大了与基体的接触面积,能够使纤维更好地与环氧树脂基体间发生界面结合,进而有效改善芳纶Ⅲ-环氧复合材料的界面黏接强度。     

Effects of environmental exposure on fiber/epoxy interfacial shear strength

The TRI microbond technique for direct determination of fiber/resin interfacial shear strength in composites has been used for investigation the influence of environmental conditions on adhesive bonding in certain systems. The small dimensions involved in the method facilitate uniform exposure and short exposure times. We have observed significant changes in both average shear strength and in shear strength distributions on exposing aramid/epoxy and glass/epoxy microbond assemblies to steam or hot water. Shear strength dropped to a plateau value in both cases, the reduction being more drastic with the glass fiber. Vacuum drying restored shear strength completely in aramid/epoxy microassemblies, even when the surface of the aramid fiber had been chemically modified, but there was only partial regeneration of bond strength with the glass/epoxy system.     

表面改性芳纶复合材料的界面粘结与界面断裂韧性

本文以表面改性芳纶和改性ＢＭＩ型树脂组成复合材料体系，研究芳纶表面改性其复合材料界面粘结与界面断裂韧性的影响。     

杂环芳纶表面ZnO纳米界面相的构筑及其界面强化作用

为了改善杂环芳纶(F3)与环氧树脂黏结性差以及不耐紫外辐射的缺点,首先对纤维进行功能化预处理,然后通过溶胶-凝胶法和水热法分别在芳纶表面生长了氧化锌纳米颗粒和氧化锌纳米线界面层。采用X成、形貌、与环氧树脂的黏结性以及抗紫外性能进行了研究。结果表明:纳米颗粒状和纳米线形态的ZnO纳米界面相能够显著提高纤维与树脂基体的黏结性能,与未处理的纤维相比,单纤维复合材料的界面剪切强度分别提高了14.1%和27.0%;同时ZnO的破坏,经过168 h紫外辐射试验后,纤维强度保持率从79.1%提高到96.7%。     

电子束辐射接枝对PAN基碳纤维的表面改性

采用电子束加速器辐射接枝方法对聚丙烯腈(PAN)基碳纤维进行表面改性,研究了接枝单体种类对接枝率及其环氧树脂基复合材料力学性能的影响,分析了辐射接枝前后PAN基碳纤维的表面形貌与化学结构以及其复合材料界面断口的形貌变化。结果表明:电子束辐射接枝改性的PAN基碳纤维表面粗糙度增加,表面活性官能团增多,与树脂的机械锲合作用增强,其树脂基复合材料断口表而较为平整;乙二胺/水溶液体系是辐射接枝改性的理想溶液,在200 kGy的电子束辐射下,PAN基碳纤维表面的接枝率为6.66%,复合材料的层间剪切强度提高了45.1%。     

芳纶纤维增强树脂基复合材料的界面粘结性能研究

为了改善芳纶纤维增强树脂基复合材料的界面粘结性能,从树脂基体入手,依据相似相容原理和芳纶的结构特点,合成出新型热固性树脂(AFR–T)用作芳纶复合材料的基体,以未经表面处理的芳纶作增强材料,采用热压成型法制备了AFR–T/芳纶纤维复合材料,并通过测定溶度参数、接触角、线膨胀系数、层间剪切强度(ILSS)和横向拉伸强度等方法研究了复合材料的界面粘结性能。结果表明,AFR–T树脂浇注体与芳纶的溶度参数相近,AFR–T树脂溶液在芳纶纸表面的接触角为36.9°,小于环氧树脂(EP)溶液与芳纶纸的接触角(53.2°),说明AFR–T树脂对芳纶的浸润性优于EP;AFR–T/芳纶纤维复合材料的ILSS和横向拉伸强度为73.0 MPa和25.3 MPa,分别比EP/芳纶纤维复合材料提高了25.9%和32.5%,这表明AFR–T树脂与芳纶纤维之间的浸润性和界面粘结性能较好。