聚乙烯/ 石墨纳米复合材料的制备、结构和导电性

用溶液插层(SI ) 和母料熔体混合(MMM ) 方法制备了聚乙烯(PE ) / 马来酸酐接枝聚乙烯(gPE ) / 膨胀石墨(EG) 导电纳米复合材料, 以直接熔体混合(DMM ) 法制备的PE/ gPE/ EG、PE/ EG复合材料作对照, 通过电导率(σ) 测试, TEM、SEM、OM 观察和DSC 分析, 研究了制备方法、EG体积或质量分数( ? 或f_m ) 和gPE质量含量( C_g ) 对复合材料结构和σ的影响。结果表明, SI、MMM、DMM 法制备的C_g/ f_m = 115 复合材料和PE/ EG对照材料的逾渗阈值?_c 分别为2.19 %、3.81 %、4.68 %和5.35 %;当C_g/ f_m 由1 增至4 时, MMM、DMM 法制备的f_m = 9 %复合材料的σ分别跃升12 和8 个数量级;产生这些差异和现象的原因, 可根据复合材料中EG分散相形态和内部微结构随制备方法、?和C_g/ f_m 的变化, 按逾渗理论来解释。     

SiC颗粒增强铝合金基梯度复合材料拉伸力学性能及其评价

对SiC颗粒增强铝合金基梯度复合材料的拉伸力学性能进行了研究。提出了一种新的材料力学性能评价指标——梯度系数K_x。理论研究表明,金属基梯度复合材料(MMGC)各组分性能的差异使其在拉伸变形时产生了三轴应力。实验及断口分析表明,由拉伸试验获得的材料平均力学性能指标弹性模量E和屈服强度σ_0.2近似符合ROM法则;此类材料的拉伸力学性能受SiC颗粒梯度分布方式的影响。外层为基体,芯部为高SiC含量的材料拉伸断口具有韧性断裂特征,能发挥其性能优势。反之,断口表现出脆性断裂特征,降低了材料的力学性能;受多种因素影响,裂纹穿过层间界面时,会引起断裂方式和扩展方向的改变。当梯度层间SiC颗粒体积分数相差较大时,材料会产生分层开裂;梯度系数K_σb和K_δ可反映材料的梯度分布方式和性能的优劣程度,梯度系数K_E则反映了材料性能的稳定性程度。     

自生复合Al11La3/Al共晶材料的轴向拉伸性能及其断裂机制

本文研究了自生复合Al₁₁La₃/Al共晶材料从室温到673K时的轴向拉伸性能和轴向拉伸断裂机制.结果表明:在G=700K/cm、R=11.1μm/s的定向凝固条件下,该材料轴向拉伸性能在室温时为260MPa、在673K时为265MPa.对拉伸过程的动态观察和断口形貌的分析表明:自生复合Al₁₁La₃/Al共晶材料在室温到673K温度范围内,其轴向拉伸断裂机制相同:纤维相Al₁₁La₃的断裂是整个共晶体断裂的控制机制:其轴向拉伸的断裂模型为:弹性变形、裂纹萌生、界面脱粘、搭桥过程、宏观断裂.     

再生PET纤维/PP复合材料的结构及力学性能

为满足环境保护和可持续发展的需要,废弃无纺布的回收再利用已经成为材料领域的又一研究热点。本文以废弃无纺布为研究对象制得再生聚对苯二甲酸乙二醇酯(PET)纤维,通过热压成型技术制备不同纤维含量的PET/聚丙烯(PP)复合材料。综合利用SEM、DSC、XRD、拉伸性能测试等手段对PET/PP复合材料的结构和性能进行了研究。结果表明:低含量的PET纤维均匀分散在PP基体中,与基体间界面结合紧密;PET纤维的异相成核作用促进了PP分子链的结晶,提高了结晶度,使晶粒细化;这些微结构的变化有利于PET/PP复合膜力学性能的提高,当PET纤维含量仅为0.1%时,PET/PP复合膜的拉伸强度提高了25.99%,断裂韧性提高了61.96%。     

复合材料层板+θ/-θ层间断裂韧性研究

本文讨论了纤维增强复合材料层板沿+θ/-θ层间断裂韧性的研究方法;提出在满足一定力学条件时,可沿用机械载荷实验方法测得G_C中“纯机械部分”G_m;结合数值方法计算得出“纯温度部分”G_T,从而得到G_C.给出一个针对DCB试验的充分条件,据此设计铺层并对T300/648和T300/QY8911进行试验和分析(θ=0～30°)、讨论了大变形的影响并提出一个新的修正系数.结合θ对G_C的影响及断口微观形貌作了进一步讨论.     

(Al2O3)f/Al复合材料在强界面结合下的疲劳损伤模式

在拉-拉载荷下测定了(Al₂O₃)_f/Al复合材料的疲劳寿命(S-N)曲线。通过夭折试验以及SEM疲劳断口和纵截面组织结构分析,研究了复合材料的疲劳损伤模式。研究结果表明,(Al₂O₃)_f/Al复合材料的疲劳极限为750MPa,远高于SCS-6碳化硅纤维增强钛基复合材料。该复合材料兼有钛基和树脂基纤维复合材料疲劳损伤的特点,高应力下由单个裂纹的起源和生长导致复合材料的失效;低应力下,疲劳损伤模式包括纤维劈裂、众多基体裂纹和单个基体裂纹的横向扩展。其中纤维劈裂是主控机制。其更高的疲劳极限可归因于低应力下纤维的纵向劈裂。     

任意铺层开裂复合材料层板本构关系探讨及特例分析

本文作者对含非正交各向异性铺层的约束开裂复合材料层板,提出用分解刚度的方法建立本构关系;给出分解后耦合问题的控制微分方程;作为特例,研究了(-θ_m/90_n/θ_m)_s开裂层板的刚度衰减.     

累托石/热塑性聚氨酯弹性体纳米复合材料的制备与性能

将累托石(REC)有机化处理后通过熔融插层复合法制备了REC/热塑性聚氨酯弹性体(TPUR)纳米复合材料,并用傅立叶变换红外光谱仪(FTIR),X-射线和扫描电镜(SEM)等进行了表征。研究结果表明:十二烷基芳基季铵盐(C₁₂)对REC的处理效果及在TPUR中的分散性优于十六烷基季铵盐(C₁₆)和联苯胺(BZD);少量有机化处理REC(分别记作C₁₂-REC,C₁₆-REC和BZD-REC)加入TPUR就可使复合材料的力学性能大幅度提高,其中C₁₂-REC/TPUR的拉伸和撕裂强度在2 wt% C₁₂-REC含量时分别由38.87 MPa和92.8 kN/m提高到57.93 MPa和123.37 kN/m ,增幅分别达49 ％和33 ％;初步考察了有机化处理条件对力学性能的影响,结果发现:用处理2h的REC制备的纳米复合材料性能最佳。     

PET-MFIAA/ PP原位成纤复合材料的形态结构及力学性能

用钉挂预埋多功能界面活化剂(MFIAA)的PET(PET-MFIAA)与PP共混 - 挤出 - 拉伸,制备了PET-MFIAA/PP原位成纤复合材料,采用扫描电镜、偏光显微镜观察和力学性能测定的方法,研究了PET-MFIAA/PP的PET微纤形态、试样断面形态及力学性能,并与PET/PP、MFIAA/PET/PP两种原位成纤复合材料进行对比。结果表明: PET-MFIAA/PP PET微纤与PP基体间具有强的相互作用,PET微纤呈粗细不均匀、凹凸不平的异形形态及柔性界面等结构特征,形成了强的界面结合,其刚性、韧性均比纯 PP明显提高,含7.00% MFIAA的PET-MFIAA/PP复合材料的拉伸屈服应力、弯曲弹性模量和悬臂梁缺口冲击强度分别达到了纯PP的1.04倍、1.23倍和1.79倍。     

纳米SiO2表面接枝聚合改性及其聚丙烯基复合材料的力学性能

分别用苯乙烯和丙烯酸乙酯对纳米SiO₂进行辐照接枝聚合改性,通过两步熔融共混工艺与聚丙烯(PP)共混制备了SiO₂/PP复合材料。研究了SiO₂添加量和表面接枝不同聚合物的SiO₂对复合材料力学性能的影响。结果表明,接枝改性的SiO₂对PP有较好的增强增韧效果;拉伸断面观察显示复合材料韧性的提高主要由基体剪切屈服所致。对断面上个别较大团聚体分析发现,经辐照接枝聚合改性的纳米粒子团聚体的结构变得更加紧凑、结实,且随粒子表面聚合物的性质不同,团聚体与基体树脂的界面粘结也随之不同,导致其拉伸破坏形状有所差异,但与基体树脂的界面粘结都得到较好的改善。     

聚对苯二甲酸乙二醇酯/锡氟磷酸盐玻璃复合材料原位成纤对聚丙烯的增强效果

采用低玻璃化转变温度的锡氟磷酸盐玻璃(Pglass)改性聚对苯二甲酸乙二醇酯(PET),制备低黏度高模量的PET基复合材料(PET/Pglass);以PET/Pglass或PET为成纤相,聚丙烯为基体,利用实验室自主设计的多级拉伸挤出装置,制得原位成纤增强聚丙烯复合材料,并研究成纤相形态及其对复合材料力学性能的影响。结果表明,与PET相比,PET/Pglass在多级拉伸挤出过程中原位成纤更容易,纤维长径比更大,分散更均匀,从而进一步提高聚丙烯的拉伸强度和模量,而且能保持聚丙烯较高的断裂伸长率,表明具有低黏高模的PET/Pglass对聚丙烯的原位成纤增强效果更显著。     

Tensile properties and meso-scale mechanism of weft knitted textile composites for energy absorption

The investigation on large deformation tensile properties and the relevant meso-scale mechanisms of weft knitted textile composites is presented. The correlation between fabric structure (e.g. loop height and width, number of wale or course per unit length, etc.), matrix damage and material properties are described. Weft knitted fabrics with 1×1 interlock structure were used as the preform for the composites. The materials studied include knitted nylon fabric/unsaturated polyester resin and co-knitted polyethylene terephthalate (PET)/polypropylene (PP) textile composites. The results show that all the nylon/polyester thermoset textile composites samples displayed an ideal bi-linear character in their tensile stress–strain curves, whilst the tensile curves of PET/PP co-knitted thermoplastic samples along the wale, course and 45° directions are all significantly non-linear. The tensile behavior is superior in the wale direction to those in the course and 45° directions. The deformation mechanisms in meso-scale were identified experimentally by in-situ observation of large deformation process for both thermoset matrix and thermoplastic matrix textile composites. For the nylon/polyester composite samples, the non-linear properties mainly come from the change in the configuration of the fabric structure during extension. For the PET/PP co-knitted textile composite samples, the inelastic properties are attributed to the damage evolution in the matrix, interface damage between fiber bundle and matrix, sliding between the wales of the knitted fabric, as well as the change in the configuration of the fabric structure during loading.     

抗静电PET/ATO纤维的制备及材料的性能

采用原位聚合的方法制备了抗静电涤纶(PET)/锑掺杂二氧化锡(ATO)纳米复合材料。结果显示,ATO在PET中分散良好,团聚体尺寸小于200 nm;加入ATO没有影响PET的流动曲线类型,随着ATO含量的增加,在相同的剪切频率下,熔体黏度均呈先增加后减小的趋势;加入ATO提高了材料的热性能,利于熔融纺丝。采用熔融纺丝法制备了抗静电纳米复合纤维。ATO含量为1.0%(质量分数,下同)时纤维的比电阻由2.7×1013Ω.cm下降到4.9×108Ω.cm。抗静电纤维的渗滤阈值为1.05%,低于传统抗静电填料。     

聚丙烯/热致液晶聚合物/玻璃纤维混杂复合材料 Ⅱ: 混杂复合材料的静态及动态力学性能

对具有良好液晶聚合物微纤结构的聚丙烯/热致液晶聚合物/玻璃纤维 (PP/TLCP/GF) 混杂复合材料,使用静态拉伸和动态力学分析 (DMA) 的方法研究了材料的力学性能。拉伸实验结果表明,混杂复合材料的拉伸强度和模量随着PP和TLCP挤出后的牵伸速率增大而上升,并且含有增容剂PP-g-MAH的体系,力学性能更优异。DMA测试结果表明,混杂复合材料的动态模量E'随着体系中玻纤的含量增加而增大;当体系中加入增容剂后,复合材料的刚性得到进一步提高。但无论是否使用了增容剂PP-g-MAH,当体系中玻纤含量高于20%后,模量随玻纤含量增大的趋势变缓。当体系中增强相的含量增加,以及加入增容剂使增强相与基体的界面粘结得到改善后,PP基体的损耗因子 (tanδ) 峰值都有一定的减小。      

聚丙烯/热致液晶聚合物/玻璃纤维混杂复合材料Ⅰ: 液晶聚合物组分的预成纤及对混杂复合材料形态的控制

考察了熔融挤出后施加的牵伸比和增容剂对聚丙烯 (PP)/热致液晶聚合物(TLCP) 原位复合材料中TLCP分散相形貌的影响。结果表明,复合材料中的TLCP相随着牵伸比的增大逐渐形成良好的微纤结构,TLCP微纤的长径比随牵伸比增大而增大;当体系中加入增容剂PP-g-MAH后,体系中TLCP在较小的牵伸速率下即可形成长径比很大的微纤结构。将上述所得原位复合材料与玻纤在 200℃(低于TLCP熔融温度) 下熔融挤出制得玻纤和液晶聚合物微纤混杂增强的材料。实验证明,在此加工温度下液晶聚合物形态得到较好保持,注射样品中不存在原位复合材料中典型的"皮-芯"形貌。同时,增容剂PP-g-MAH还明显改善了玻纤与基体之间的界面粘结。      

Effect of composition on phase morphology and mechanical properties of PP/PA66 in situ composites via extrusion-drawing-injection method

The reinforced and toughened PP/PA66 in situ composites were prepared via extrusion-drawing-injection method. The relationship among composition, phase morphology and mechanical properties, together with their functional mechanism, was investigated. The results show that in the range of PA66 weight fraction (f _w) from 0 to 20% and under the experimental processing conditions, the main changes in phase morphology of the composites with f _w are that the number of in situ formed PA66 microfibers and remained PA66 particles increases with f _w whereas the fiber transverse size and its dispersity decrease till f _w = 15% and then increase. This can be attributed to the combined effect of break-up, coalescence and deformation of the PA66 phase in the PP phase in the course of extrusion and drawing. The tensile strength of composites has a maximum value at f _w of 15% and Young's modulus increases with f _w up to a plateau level, while impact strength continuously rises with f _w, an effect which can be ascribed to the distinct dependence of these properties on the phase-morphological factors mentioned above.     

Ternary nano-CaCO3/poly(ethylene terephthalate) fiber/polypropylene composites: Increased impact strength and reinforcing mechanism

The binary nano-CaCO₃/polypropylene (PP), poly(ethylene terephthalate) (PET) fibers/PP and ternary nano-CaCO₃/PET fibers/polypropylene composites were prepared by melt blending method, and their structure and mechanical properties were investigated. The results show that the ternary nano-CaCO₃/PET fibers/PP composite displays significantly enhanced mechanical properties compared with the binary PET fibers/PP and nano-CaCO₃/PP composites, and neat PP. The X-ray diffraction, dynamic mechanical analysis, scanning electron microscopy and analysis of the non-isothermal crystallization kinetics were used to investigate the reinforcement mechanism of composites. The results indicate that the interfacial action and compatibility between PET fiber and PP are obviously enhanced by the addition of modified nano-CaCO₃ particles in the ternary composites and the mechanical property enhancement in the ternary system may be mainly originated from the formation of β-form crystallites of PP induced by the synergistic effect between PET fibers and nano-CaCO_3.     

Ceramic composites: roles of fiber and interface

Results are presented that elucidate: (a) the effects of fiber coating on retained fiber strength and mechanical properties of Nicalon-fiber-reinforced SiC matrix composites; and (b) the role of residual stresses in the interfacial bond strength of SiC-fiber-reinforced reaction-bonded Si₃N₄ matrix composites. For Nicalon-fiber-reinforced SiC matrix composites that were fractured in a flexural mode, retained in-situ fiber strength, ultimate strength and work-of-fracture (WOF) of the composites increased with increasing thickness of the fiber coating and reached maximum values at a coating thickness of ≈0.3 μm. A direct correlation between the variation of in-situ fiber strength and the variation of ultimate strength and WOF of the composites clearly indicates the critical role of the retained in-situ strength of reinforcing fibers in composites. Fiber pushout tests performed on SiC-fiber-reinforced reaction-bonded Si₃N₄ matrix composites indicate that both debonding and frictional shear stresses decreased with increasing fiber content. These variations are consistent with the variation of residual radial stress on fibers, as measured by neutron diffraction, i.e. residual stresses decreased with increasing fiber content. Because fracture behavior is strongly controlled by interfacial bond strength, which is proportional to the residual radial stress, appropriate control of residual stresses is critical in the design of composites with desired fracture properties.     

纳米CaCO_3/PET短纤维/聚丙烯复合材料的制备及性能

制备了纳米CaCO3/聚丙烯、聚对苯二甲酸乙二酯(PET)短纤维/聚丙烯、CaCO3/PET短纤维/聚丙烯复合材料。分别测试了复合材料的力学性能,结果发现,与纳米CaCO3/聚丙烯、PET短纤维/聚丙烯两相复合材料相比,三相复合材料的力学性能尤其是冲击性能有明显的提高。采用X射线衍射(XRD)、动态力学分析(DMA)、电子扫描(SEM)系统研究了复合材料的增强机理,结果发现,在三相复合材料中,纳米CaCO3的加入明显提高了PET短纤维与聚丙烯基体界面之间的作用力和相容性,同时纳米CaCO3与PET短纤维的协同效应诱导了聚丙烯β晶的生成。