F-12和国产芳纶Ⅲ纤维/环氧单向复合材料力学性能和强度对比分析

采用单向复合材料缠绕型式,对F-12和国产芳纶Ⅲ纤维增强环氧复合材料进行力学性能测试,考核了两种芳纶纤维/环氧复合材料界面黏结性能,并进行拉伸破坏机理与强度分析,获得了强度参数值.结果表明:两种芳纶纤维单向复合材料具有明显的各向异性特征,轴向力学性能远高于径向力学性能;F-12/环氧复合材料力学性能优于国产芳纶Ⅲ/环氧复合材料性能;两种复合材料纤维/树脂界面粘接较差.     

纳米SiO2改性EP对基体力学性能和芳纶纤维/EP复合材料界面性能的影响

研究了纳米SiO2对环氧树脂(EP)基体力学性能的影响,并进一步采用对位芳纶纤维(F-12)增强环氧树脂,制备了NOL环复合材料,通过复合材料层间剪切性能测试考核了F-12与环氧树脂之间的界面粘接性能.结果表明:环氧树脂中添加适量的纳米SiO2能够有效提高环氧树脂浇注体的拉伸强度、拉伸弹性模量、冲击强度.纳米SiO2的加入,可以有效改善F-12与环氧树脂基体之间的界面粘接性能,降低复合材料的空隙率,F-12/纳米SiO2(6%)-EP复合材料的层间剪切强度(ILSS)提高约60.3%.     

低温等离子体对PBO纤维表面的改性

采用硅烷偶联剂处理聚对苯撑苯并双噁唑(PBO)纤维,利用常压射频低温等离子体对PBO纤维进行了表面处理,通过扫描电镜、红外光谱、光学显微镜等研究了处理时间对PBO纤维表面官能团和表面形貌的影响规律,通过单丝拔出实验测定PBO纤维基复合材料的界面剪切强度。结果表明:经过常压射频低温等离子体处理后,PBO纤维的表面形成了大量的极性基团,表面产生明显的凹坑,PBO纤维与树脂的粘接性能提高50%,纤维的拉伸强度下降5%。     

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。     

芳纶纤维/AFR树脂复合材料界面粘结性能的研究

为了改善芳纶纤维复合材料的界面粘结性能,合成了一种新型树脂(AFR)作为基体,以未经任何表面处理的芳纶纤维作增强材料,制备了芳纶纤维/AFR复合材料。采用测定表面能、接触角、层间剪切强度、横向拉伸性能和扫描电镜观察形貌等方法,从宏观和微观等方面研究了芳纶纤维/AFR复合材料的界面粘结性能。结果表明,AFR树脂与芳纶纤维有相近的表面能,AFR树脂溶液与芳纶纤维的接触角为42.8°,而环氧树脂(EP)与芳纶纤维的接触角为68°,说明AFR树脂对芳纶纤维的润湿性优于EP树脂;芳纶/AFR复合材料的层间剪切强度、横向拉伸强度和纵向拉伸强度分别为74.64MPa、25.34MPa和2256MPa,比芳纶/EP复合材料的相应强度分别提高了28.7%、32.5%和13.4%,其复合材料破坏面的形貌也说明芳纶纤维与AFR树脂之间的界面粘结性能较好。     

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.     

环氧树脂/PBO纤维复合材料性能研究

对环氧树脂(EP)/聚对苯撑苯并二恶唑(PBO)纤维复合材料的性能进行初步研究。结果表明,用浓度70%的甲基磺酸(MSA)溶液对PBO纤维表面进行处理,可改善PBO纤维与EP基体的粘结强度,但同时使PBO纤维的拉伸性能降低;对PBO纤维处理2h后,以胺类固化剂固化的EP/PBO纤维复合材料的层间剪切强度比处理前提高41%,以酸酐固化剂固化的EP/PBO纤维复合材料的层间剪切强度比处理前提高48%;前者的层间剪切强度大于后者。     

芳纶/环氧复合材料性能研究

对国产芳纶Ⅲ/环氧及F-12/环氧复合材料的力学性能,与绝热层材料的相容性、3个热常数、微观断裂形貌等进行了系统地测试、比对和分析.结果表明,芳纶Ⅲ复合材料的抗弯曲、压缩、剪切和横向拉伸性能均低于相应的F-12复合材料,但具有优越的抗纵向拉伸强度,其抗纵向拉伸强度比F-12复合材料高约13.9%;芳纶复合材料与丁腈橡胶的抗两板剪切性能略高于芳纶复合材料与三元乙丙橡胶的抗两板剪切性能.总体上来说,芳纶复合材料属于隔热性能较好的材料,但其抗剪性能、纵向抗压性能较差.SEM可观察到芳纶复合材料破坏断口呈"皮芯"抽离和纤维撕裂的破坏特征.     

PBO纤维表面改性方法的研究

对PBO纤维表面性能的改善进行了研究,考察了混杂芳纶纤维、电晕处理、偶联剂处理及强酸处理等多种方法对PBO纤维与环氧树脂表面粘接强度及其复合材料层间剪切性能的影响程度,比较了各种方法的改性效果及各自优缺点。     

PBO纤维表面特性对酚醛复合材料拉伸性能的影响

复合材料良好的界面结合可使增强纤维发挥最大的承载作用,良好的纤维表面性能有助于纤维性能转化率的提高,从而有利于其力学性能。为研究国产聚对苯撑苯并二噁唑(PBO)纤维表面特性对酚醛基复合材料拉伸性能的影响,采用扫描电子显微镜、原子力显微镜和接触角测量仪分析了三种国产高模型PBO纤维的表面特性,并计算其纤维强度转化率。研究发现,PBO纤维的表面粗糙度和沟槽等对复合材料的界面性能及纤维强度转化率具有显著影响。结果表明：三种国产PBO纤维表面均有明显的黏附物和纤维向沟槽,表面杂质少、沟槽较多,表面粗糙度最大、表面自由能最高的PBO-A纤维强度转化率最高,PBO纤维的强度转化率(40%～50%)远低于碳纤维的强度转化率(70%～90%),其与树脂的工艺匹配性有待进一步提高。     

芳纶、碳纤维混杂工艺对环氧复合材料拉伸性能的影响

研究了铺层参数及纤维表面处理对芳纶纤维、碳纤维混杂增强环氧复合材料(简称混杂复合材料)纵向拉伸性能的影响。结果表明，该混杂复合材料的纵向拉伸强度均低于混合定律的预测值，表现出明显的混杂负效应。铺层顺序对材料纵向拉伸强度及断裂伸长率有显著影响，界面数越多，纵向拉伸强度和断裂伸长率越大；界面粘接性能的改善可提高混杂复合材料的拉伸强度和断裂伸长率，但对它的弹性模量没有显著影响。     

Evaluation of fiber surfaces treatment and sizing on the shear and transverse tensile strengths of carbon fiber-reinforced thermoset and thermoplastic matrix composites

The mechanical performance of advanced composite materials depends to a large extent on the adhesion between the fiber and matrix. This is especially true for maximizing the strength of unidirectional composites in off-axis directions. The materials of interest in this study were PAN-based carbon fibers (XA and A4) used in combination with a thermoset (EPON 828 epoxy) and a thermoplastic (liquid crystal poymer) matrix. The effect of surface treatment and sizing were evaluated by measuring the short-beam shear (SBS) and transverse flexural (TF) tensile strengths of unidirectional composites. Results indicated that fiber surface treatment improves the shear and trasverse tensile strengths for both thermosetting and thermoplastic matrix/carbon fiber-reinforced unidirectional composites. A small additional improvement in strengths was observed as the result of sizing treated fibers for the epoxy composites. Scanning electron microscope photomicrographs were used to determine the location of composite failure, relative to the fiber-matrix interface. Finally, the epoxy composites SBS and TF strengths appear to be limited to the maximum transeverse tensile strength of the epoxy matrix, while the thermoplastic composite SBS and TF strengths are limited by the LCP matrix shear and transverse tensile strengths, respectively.     

Effect of Surface Modification on Mechanical and Tribological Performance of Poly-p-phenylenebenzobisoxazole Fiber-Reinforced Polyimide Composite

This work examined the effect of coupling agent surface modification of Poly-p-phenylenebenzobisoxazole (PBO) fibers on mechanical and tribological performance of PBO fiber-reinforced thermoplastic polyimide (PBO/PI) composites. The results show that tensile strength and flexural strength are largely improved by coupling agent treatment. Under dry sliding conditions, coupling agent treatment is effective to reduce the wear of PBO/PI composite. The principle of improvement in interfacial adhesion between PBO fiber and PI matrix after coupling agent treatment was discussed. The surface characteristics of PBO fibers were characterized by X-ray photoelectron spectroscopy (XPS). It is found that the content of polar groups on the surface of PBO fiber treated by coupling agent increases compared with the untreated fiber. The presence of polar groups is probably leading to an increment of interfacial binding force between fibers and matrix in a composite system, and accordingly enhances the mechanical and tribological properties.     

国产PBO纤维的性能及形貌研究

采用扫描电子显微镜、元素分析仪、热分析仪以及复合材料单向环(NOL)法等对国产聚对苯撑苯并双噁唑(PBO)纤维和东洋纺Zylon纤维的形貌、元素组成、热性能和力学性能进行了比较分析。结果表明:Zylon纤维单丝直径约为12μm,国产PBO纤维直径稍大,约为20μm;Zylon纤维表面较为光滑和致密,国产PBO纤维表面存在微小的浅沟槽;国产PBO纤维的断裂强度最高达5.36 GPa,模量最大为239 GPa,分别比Zylon纤维低7.6%和14.6%,但其NOL环的层间剪切强度最高达26 MPa,比Zylon纤维制备的复合材料高14%;国产PBO纤维与Zylon纤维的组成基本一致,但其耐热性能优异,在氮气中的分解温度大于676℃,在空气中的分解温度大于634℃,分别比Zylon纤维高6℃和23℃。     

Effects of PBO fiber and clay on the mechanical,morphological, and dynamic mechanical properties of NR/HDPE blends

Poly(p‐phenylene‐2,6‐benzobisoksazole) (PBO) and natural rubber (NR)/high density polyethylene (HDPE) composites were melt‐blended in a Haake internal mixer. The tensile strength, tensile modulus, and impact strength increased with fiber loading and optimized at 20%. Incorporation of clay into the NR/HDPE/PBO composites resulted in an improvement of tensile strength for NR/HDPE/PBO composites compared to the systems without clay. However, addition of clay was only effective at low contents (5–7.5%). Additional improvement of tensile strength, tensile modulus, and impact strength of the hybrid composite was observed on addition of liquid natural rubber (LNR). Scanning electron micrographs of the samples had indicated that the presence of clay decreased the domain size of the dispersed phase. Results on dynamic response showed that incorporation of clay and LNR into the composites had increased the storage modulus and reduced the tan δ. The shift of glass transition temperature (T_g) to higher values for composites also indicated good interaction between the fiber and the matrix. POLYM. ENG. SCI., 2011. © 2010 Society of Plastics Engineers.     

单向芳纶/玻璃纤维混杂复合材料板材拉伸性能研究

本文对单向芳纶/玻璃纤维复合材料进行制作,对其纵向拉伸强度、拉伸模量和弹性伸长进行实验分析。实验结果表明,单向混杂复合材料的拉伸断裂大多为多次性,界面数越多,一次性断裂的可能性越大。界面数为1的混杂纤维复合材料的芳纶纤维体积含量在对拉伸强度影响上的存在临界值,表现出明显的混杂效应。界面数大于1的混杂复合材料在芳纶纤维铺层数一定的情况下,界面数的多少不影响混杂复合材料拉伸强度和拉伸弹性模量的大小。界面数大于1比界面数为1的复合材料的拉伸强度和拉伸模量明显偏高。同时对不同制作条件下纯玻璃纤维单向复合材料的拉伸性能进行剖析。     

PBO纤维表面改性与热处理研究

运用扫描电镜对自制的聚对苯撑苯并二噁唑(PBO)纤维表面进行观察,发现未经烘干的PBO纤维表面有许多的裂纹和沟槽,而烘干的纤维表面则较光滑。通过单丝拔出实验研究了偶联剂对不同表面形态纤维的表面处理情况,结果表明:用偶联剂表面处理后,纤维与树脂间的界面剪切强度得到提高,偶联剂对未经烘干纤维表面处理比对烘干纤维处理的效果要好,与原丝相比,提高率可达69.4%。对自制的PBO纤维进行了热处理,发现未烘干的PBO纤维比经烘干而干燥致密化的纤维的热处理效果要好,模量有很大提高,强度也有一定的增加。     

Effect of coupling agents on the thermal and mechanical properties of polypropylene–jute fabric composites

Composites with different jute fabric contents and polypropylene (PP) were prepared by compression molding. The composite tensile modulus increased as the fiber content increased, although the strain at break decreased due to the restriction imposed on the deformation of the matrix by the rigid fibers. Moreover, and despite the chemical incompatibility between the polar fiber and the PP matrix, the tensile strength increased with jute content because of the use of long woven fibers. The interfacial adhesion between jute and PP was improved by the addition of different commercial maleated polypropylenes to the neat PP matrix. The effect of these coupling agents on the interface properties was inferred from the resulting composite mechanical properties. Out‐of‐plane instrumented falling weight impact tests showed that compatibilized composites had lower propagation energy than uncompatibilized ones, which was a clear indication that the adhesion between matrix and fibers was better in the former case since fewer mechanisms of energy propagation were activated. These results are in agreement with those found in tensile tests, inasmuch as the compatibilized composites exhibit the highest tensile strength. Scanning electron microscopy also revealed that the compatibilized composites exhibited less fiber pullout and smoother fiber surface than uncompatibilized ones. The thermal behavior of PP–compatibilizer blends was also analyzed using differential scanning calorimetry, to confirm that the improvements in the mechanical properties were the result of the improved adhesion between both faces and not due to changes in the crystallinity of the matrix. Copyright © 2006 Society of Chemical Industry