酚醛-石英混杂纤维增强苯并噁嗪复合材料高温失效特征

通过模压工艺制备了酚醛-石英混织纤维增强苯并噁嗪复合材料(P-Q/BZ)试样,考察了其力学性能、烧蚀性能和耐冲刷性能,分析了该试样在高温环境中的主要失效特征,研究其在高温环境中的适用性。结果表明,未经热处理的P-Q/BZ试样平均弯曲强度、弯曲模量和层间剪切强度分别为283 MPa、10.8 GPa和22.6 MPa;经300℃,N_2处理15 min后,试样均匀膨胀,厚度增加22%,弯曲强度、弯曲模量和层间剪切强度分别下降58%、41%和58%;在氧乙炔焰的平均质量烧蚀率和线烧蚀率分别为0.048 4 g/s和-0.081 mm/s,烧蚀后试样宏观不分层,表面炭层微观分层严重,酚醛纤维热解炭、树脂基体热解炭、熔融石英纤维以及碳硅氧化产物相互分离;该试样耐冲刷能力差,在发动机尾焰烧蚀平台模拟的热-力耦合环境中的质量损失率高达59%。P-Q/BZ复合材料需要解决热解膨胀问题,进一步提高抗冲刷性能。     

石英/双酚E型氰酸酯复合材料的制备与性能

采用实验方法研究双酚E型氰酸酯树脂的黏度和固化特性,揭示催化剂对双酚E型氰酸酯树脂固化特性的影响规律;采用树脂传递模塑和真空导入模塑工艺制备石英纤维/双酚E型氰酸酯复合材料,并考察其力学性能。结果表明,双酚E型氰酸酯树脂室温至90℃范围内的黏度小于300 m Pa·s,凝胶时间大于10 h,起始固化温度、固化温度和终止固化温度分别为186±5℃,235±5℃和286±5℃;固化特征温度随着催化剂含量的增加而降低,直至催化剂饱和,其饱和范围为0.02%~0.03%,可使双酚E型氰酸酯树脂体系的固化温度降低约60℃,从而避免爆聚,实现液相法成型其复合材料;真空导入模塑工艺制备的石英纤维/双酚E型氰酸酯复合材料的力学性能明显优于树脂传递模塑制备试样。     

3维C/SiC-ZrC复合材料的制备及其性能研究

针对超高温环境应用需求,采用化学气相渗透工艺(CVI)与先驱体浸渍-裂解工艺(PIP)联用制备了3维碳纤维增强SiC-ZrC基复合材料(C/SiC-zrC),并研究了SiC含量对C/SiC-ZrC复合材料力学性能、抗氧化性能和抗烧蚀性能的影响.结果表明,随着SiC含量的增加,C/SiC-ZrC复合材料的强度逐渐降低,静...     

三维石英纤维增强氮化物基复合材料的烧蚀性能及显微结构

采用先驱体转化法制备了三维石英纤维增强氮化物基复合材料(3D SiO2f/Si3N4-BN),用等离子射流烧蚀方法研究了复合材料的烧蚀性能,运用扫描电镜及能谱仪对烧蚀表面微观形貌进行了观察和分析。结果表明氮化物基复合材料在高压高热流等离子体烧蚀下线烧蚀率为0.91mm/s,石英纤维熔融并被吹除带走了大量的热量,熔融层抑制了基体的机械剥蚀。基体由于强度高、升华温度高,延缓了熔融层的吹除,表明氮化物基复合材料是一种良好的耐高温烧蚀透波材料。     

列车用复合材料阻燃性能研究

不同类别的阻燃剂配合使用能产生协效作用,大大提高阻燃效果。在甲基丙烯酸类不饱和聚酯树脂9001基体中,添加微囊化红磷/氢氧化铝/三氧化二锑/甲基膦酸二甲酯(MRP/Al(OH)3/Sb2O3/DMMP)阻燃剂体系,对其树脂体系固化物及玻璃纤维织物复合材料的力学性能和阻燃性能进行了实验研究,提出了一种有望用于列车复合材料大尺寸构件制造的性能优异、价格低廉的新体系。结果表明,当质量添加比例分别为12%MRP、50%Al(OH)3、2%Sb2O3时,树脂体系室温粘度100mPa.s左右,凝胶时间超过80min,适用于RTM和VIMP等大尺寸构件成型工艺;复合材料拉伸强度215.4MPa,弯曲强度177.15MPa,拉伸模量13.85GPa,弯曲模量13.36GPa,氧指数39.7。     

惰性填料对SiCf/Si-O-C陶瓷材料的性能影响

以聚硅氧烷为先驱体,采用先驱体转化法制备了SiCf/S i-O-C陶瓷复合材料.研究了惰性填料(SiC、SiO2及SiO2空心微珠)对材料的力学性能及热性能的影响.微观结构的分析表明,填料引起的界面结构与密度的变化是影响SiCf /Si-O-C复合材料性能的主要原因.     

耐海水高耐候丙烯酸树脂的合成及面漆性能分析

为合成耐海水与高耐候的丙烯酸树脂,选择甲基丙烯酸甲酯、甲基丙烯酸羟丁酯、丙烯酸异辛酯和丙烯酸已内酯,经引发剂作用,采用同步滴加法进行聚合反应,通过调节温度并测定酸价控制反应历程,并将合成的不同玻璃化温度的丙烯酸树脂配制成具有适当玻璃化温度梯度的耐海水面漆成膜树脂体系。选择HDT-90固化剂与丙烯酸成膜树脂作用,制备耐海水面漆涂层样品。性能测试结果表明,研制的耐海水面漆具有优良的耐候性和抗老化性。     

T300和JC2#纤维增强C/SiC复合材料力学性能对比

以聚碳硅烷(PCS)为先驱体,采用聚合物浸渍裂解法(PIP)分别制备得到T300碳纤维和JC2#碳纤维增强C/SiC复合材料。JC2#C/SiC复合材料具有优异的力学性能,抗弯强度和断裂韧性分别达到662MPa和19.5MPa.m1/2;T300 C/SiC复合材料表现出低强度、高脆性,其抗弯强度和断裂韧性不足前者的四分之一。T300 C/SiC复合材料低性能的根本原因在于T300纤维在PCS裂解过程中性能严重下降,复合材料中纤维与基体间存在强界面结合是另一个影响因素。     

氧化铝气凝胶复合材料的制备与隔热性能

以仲丁醇铝为先驱体,采用溶胶一凝胶工艺制备氧化铝溶胶,并将其与无机陶瓷纤维毡复合经超临界流体干燥得到氧化铝气凝胶隔热复合材料.利用扫描电子显微镜(SEM)和氮气吸附等方法对样品微观结构进行分析,利用热平板法对材料的隔热性能进行测试,并分析了氧化铝气凝胶隔热复合材料隔热机理.研究表明:与氧化硅气凝胶相比,氧化铝气凝胶具有更好的耐高温性能,经1000℃热处理后仍然能够较好地保持其纳米多孔结构;将气凝胶与纤维复合后,充分发挥了氧化铝气凝胶优良的隔热特性,使得复合材料的隔热性能较纯纤维毡有了明显的改善,其热面温度1000℃时导热系数为0.0685 W/m·K.     

裂解温度对PIP制备2D Cf/Si-O-C复合材料结构与性能的影响

以二维碳纤维布、硅树脂先驱体、SiC微粉和乙醇溶剂为原料,采用先驱体转化工艺制备了2D Cf/Si-O-C复合材料,考察了裂解温度对材料结构和性能的影响。结果表明,首周期裂解温度对制备材料的力学性能有重要影响,纤维-基体间的界面弱化是复合材料力学性能提高的主要原因;第6周期采用合适的温度裂解可提高复合材料的力学性能,其弯曲强度和断裂韧性分别达到了263.9MPa和12.8MPa.m1/2。     

添加SiC微粉对硅树脂先驱体转化3D Cf/Si-O-C材料性能的影响

以三维碳纤维织物和廉价的硅树脂为原料,采用先驱体转化工艺制备3D G/Si-O-C材料,考察了浸渍液中添加SiC填料对材料微观结构、力学性能和抗氧化性能影响.结果表明:添加适量的SiC填料有助于减少基体孔隙,改善界面结合,从而提高材料的力学性能;而SiC含量过高时,容易在材料内部形成闭孔,从而导致材料力学性能下降.当SiC微粉含量为18.2%时,材料具有最好的力学性能,弯曲强度和断裂韧度分别为421.3MPa和13.0 MPa·m1/2;而材料的抗氧化性能随着SiC微粉含量的增加而增加,当SiC微粉含量为25.0%时,材料的弯曲强度保留率最高,达到了89.5%.     

树脂浸渍裂解对气相硅反应渗透C/SiC的影响

粘胶基碳纤维毡经过CVD工艺进行沉积碳增密处理后,采用酚醛树脂浸渍—裂解对C/C素坯的密度进行调节,通过气相硅渗透反应工艺制备了C/SiC复合材料。研究了树脂浸渍—裂解对C/C素坯密度和气孔率的影响规律,分析了树脂裂解碳对C/SiC显微形貌和力学性能的影响。结果表明:随着树脂浸渍—裂解循环次数的增加,素坯密度增加,孔隙率降低;裂解碳含量为27wt%时,C/SiC复合材料的强度和模量达到最大,分别为231MPa和209GPa。通过控制裂解碳含量,可以实现对C/SiC复合材料力学性能和微观结构的裁剪。     

Effect of organo-modified montmorillonite nanoclay on mechanical,thermal and ablation behavior of carbon fiber/phenolic resin composites

The mechanical, thermal and ablation properties of carbon phenolic (C-Ph) composites (Type-I) rein-forced with different weight percentages of organo-modified montmorillonite (o-MMT) nanoclay have been studied experimentally. Ball milling was used to disperse different weight (wt) percentages (0, 1,2,4,6 wt.％) of nanoclay into phenolic resin. Viscosity changes to resin due to nanoclay was studied. On the other hand, nanoclay added phenolic matrix composites (Type-II) were prepared to study the dispersion of nanoclay in phenolic matrix by small angle X-ray scattering and thermal stability changes to the matrix by thermogravimetric analyser (TGA). This data was used to understand the mechanical, thermal and ablation properties of Type-I composites. Inter laminar shear strength (ILSS), flexural strength and flexural modulus of Type I composites increased by about 29％, 12％and 7％respectively at 2 wt.％ addition of nanoclay beyond which these properties decreased. This was attributed to reduced fiber volume fraction (％Vf) of Type-I composites due to nanoclay addition at such high loadings. Mass ablation rate of Type-I composites was evaluated using oxy acetylene torch test at low heat flux (125 W/cm2) and high heat flux levels (500 W/cm2). Mass ablation rates have increased at both flux levels marginally up to 2 wt.％ addition of nanoclay beyond which it has increased significantly. This is in contrast to increased thermal stability observed for Type-I and Type-Ⅱ composites up to 2 wt.％addition of nanoclay. Increased ablation rates due to nanoclay addition was attributed to higher insulation effi-ciency of nanolcay, which accumulates more heat energy in limited area behind the ablation front and self-propagating ablation mechanisms triggered by thermal decomposition of organic part of nanoclay.     

表面官能化对碳纳米管/环氧复合材料玻璃化转变温度及韧性的影响

通过碳纳米管的不同表面官能化,构造其与环氧树脂的不同界面。采用动态机械性能分析研究不同表面官能化碳纳米管对环氧树脂复合材料玻璃化转变温度的影响;采用摆锤冲击试验研究环氧树脂复合材料的韧性。结果表明:与纯环氧树脂相比,氨基化碳纳米管/环氧树脂复合材料的玻璃化转变温度升高,而羧基化碳纳米管/环氧树脂复合材料的玻璃化转变温度反而有所下降;碳纳米管/环氧树脂复合材料的冲击强度相比纯环氧树脂均提高了近一倍。复合材料性能的这些变化规律主要归因于不同表面官能化碳纳米管与环氧树脂基体间形成了不同的界面。     

Investigation of the mechanical and ballistic properties of hybrid carbon/ aramid woven laminates

High-performance ballistic fibers, such as aramid fiber and ultra-high-molecular-weight polyethylene (UHMWPE), are commonly used in anti-ballistic structures due to their low density, high tensile strength and high specific modulus. However, their low modulus in the thickness direction and insufficient shear strength limits their application in certain ballistic structure. In contrast, carbon fiber reinforced epoxy resin matrix composites (CFRP) have the characteristics of high modulus in the thickness direction and high shear resistance. However, carbon fibers are rarely used and applied for protection purposes. A hybridization with aramid fiber reinforced epoxy resin matrix composites (AFRP) and CFRP has the potential to improve the stiffness and the ballistic property of the typical ballistic fiber composites. The hybrid effects on the flexural property and ballistic performance of the hybrid CFRP/AFRP laminates were investigated. Through conducting mechanical property tests and ballistic tests, two sets of reliable simulation parameters for AFRP and CFRP were established using LS-DYNA software, respectively. The experimental results suggested that by increasing the content of CFRP that the flexural properties of hybrid CFRP/AFRP laminates were enhanced. The ballistic tests’ results and the simulation illustrated that the specific energy absorption by the perforation method of CFRP achieved 77.7% of AFRP. When CFRP was on the striking face, the shear resistance of the laminates and the resistance force to the projectiles was promoted at the initial penetration stage. The proportion of fiber tensile failures in the AFRP layers was also enhanced with the addition of CFRP during the penetration process. These improvements resulted in the ballistic performance of hybrid CFRP/AFRP laminates was better than AFRP when the CFRP content was 20 wt% and 30 wt%.     

UHMWPE复合材料抗爆实验研究

运用定制的聚偏四氟乙烯(PVDF)压电传感器,直接测量爆炸载荷下UHMWPE层叠无纬布和PU基体的UHMWPE复合材料内部冲击波压力峰值,对其冲击波衰减特性进行了实验研究。实验结果表明:UHMWPE复合材料对爆炸冲击波有很好的衰减作用,含有PU基体的UHMWPE复合材料比UHMWPE层叠无纬布对爆炸冲击波有更好的衰减效果。UHMWPE复合材料具有轻质、吸收冲击波效率高等特性,在爆炸冲击波防护领域有很好的应用前景。     

侧面封边对玻璃纤维增强环氧树脂基复合材料吸湿规律的影响

采用称量法和排水法联合,研究了侧面封边和未封边单向玻璃纤维增强环氧树脂基复合材料层合板试件的吸湿量和体积变化率与浸泡时间的关系,结果显示,复合材料侧面吸湿的速度远大于表面吸湿速度;侧面封边复合材料试件的饱和吸湿量为1.30％,而未封边试件的为2.26％,即与侧面封边试件相比,未封边试件的饱和吸湿量(质量比)增加了73....     

Synergistic effect of hybrid Himalayan Nettle/Bauhinia-vahlii fibers on physico-mechanical and sliding wear properties of epoxy composites

The cellulosic bast fibers are recognized as a justifiable and biodegradable substitute for producing moderate strength polymer composite materials because of their characteristics of renewability, eco-friendliness, and higher specific strength. Hence the aim of this research work is to fabricate Himalayan bast fibers (Nettle fiber (NF)/bauhinia vahlii fiber (BF)) based mono/hybrid epoxy composites at varying weight percentage of 2–6 wt% and evaluate the physical (void fraction and water absorption), mechanical (tensile strength, flexural strength, hardness) and sliding wear properties of as-fabricated composites. The 6 wt% NBF reinforced composites exhibited higher mechanical properties as compared to NF and BF composites with tensile strength of 34.04 MPa, flexural strength of 42.45 MPa, and hardness of 37.01 H_v respectively. The influence of various control factors (sliding velocity, NF/BF/NBF contents, normal load and sliding distance) on specific sliding wear rate of composites was evaluated by Taguchi (three factors at three levels) experimental design and the percentage contribution of these selected parameters on sliding wear performance was examined by Analysis of variance (ANOVA). The sliding wear property of as-developed composites was found to be greatly influenced by sliding velocity and the wear resistance was observed to be improved with the NF/BF/NBF contents. The wear mechanism of the as-fabricated composites has been elucidated by scanning electron microscopy analysis. The research outcomes demonstrated that the hybridization of Bauhinia vahlii fiber with Nettle fiber led to improve the mechanical and wear properties of epoxy composites.     

一种低黏度环氧树脂的制备及性能研究

采用一种新型增韧剂CC对环氧树脂进行增韧改性,获得一种低黏度中温固化环氧树脂体系。测试了树脂的力学性能,并通过红外光谱和动态热机械能分析等方法,对树脂的组织和性能进行了研究。结果表明：当CC的质量分数为19%时,环氧树脂的剪切强度和拉伸强度最大,分别为25.1 MPa和55.88 MPa;该环氧树脂具有较低的黏度;固化过程中各组分反应完全,树脂刚度较大,玻璃温度Tg达110.36℃。