共查询到18条相似文献,搜索用时 359 毫秒
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用端异氰酸酯基聚丁二烯液体橡胶与环氧树脂制得端异氰酸酯基聚丁二烯液体橡胶/环氧树脂聚合物(ETPB)。在ETPB中分别加入质量分数5%和10%的纳米Al2O3,并选择适宜的固化剂固化,制得ETPB/Al2O3复合材料。考查了ETPB与ETPB/Al2O3复合材料的力学性能,研究了该材料的滑动摩擦磨损率与滑动速度之间的关系,并用扫描电子显微镜(SEM)对几种材料磨损表面进行了观察。结果表明,通过填充纳米Al2O3无机粒子可显著提高ETPB的性能,当填充量为5%时,ETPB/Al2O3复合材料性能最佳。 相似文献
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Al2O3/环氧树脂复合材料导热性能的研究 总被引:7,自引:0,他引:7
分别选用纳米和超细Al2O3填料,采用直接分散法制备Al2O3/环氧树脂复合材料,研究了不同填料含量的复合材料的导热性能,并结合理论模型探讨粉体粒径对导热性能的影响.结果表明:随着Al2O3含量的增加,复合材料的导热系数增大.当加入40%的超细Al2O3填料时,复合材料的导热系数达到0.535 W/(m·K),是纯环氧树脂的3倍.实验测量值与Y. Agari模型参数均表明:超细Al2O3的体系中粒子更容易形成导热链,可以更有效地提高环氧树脂体系的导热性能. 相似文献
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纳米Al2O3/环氧树脂复合材料的制备及性能 总被引:11,自引:1,他引:11
在原位法制备纳米复合材料时,要使纳米粒子在树脂中分散均匀,必须首先获得稳定的单体悬浮体系。基于这一原理,本文通过对纳米Al2O3表面改性即选择合适的分散剂,获得稳定的纳米Al2O3/丙酮悬浮液,然后将环氧树脂溶解于其中,制得纳米Al2O3/环氧树脂复合材料。运用透射电子显微镜,观察了纳米Al2O3在环氧基体中的分散情况。分析并讨论了纳米Al2O3含量对该复合材料力学性能的影响。结果表明:利用稳定的悬浮体系能制得分散较为均匀的纳米复合材料,在纳米Al2O3含量为5%的情况下,纳米复合材料的力学性能达到最优。 相似文献
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环氧树脂/纳米α-Al2O3复合材料性能的研究 总被引:11,自引:0,他引:11
以纳米α-Al2O3作为增强材料,制备纳米复合材料,研究了不同处理方法及不同的纳米α-Al2O3质量分数对纳米复合材料性能的影响,采用透射电镜对纳米α-Al2O3粒子的分布进行了表征。结果表明,当纳米粒子α-Al2O3质量分数为2%时,复合材料的拉伸强度为61.1MPa,拉伸模量为3.42GPa,玻璃化温度为137.97℃。 相似文献
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将带有环氧基的功能性单体甲基丙烯酸缩水甘油酯(GMA)接枝聚合在微米级氧化铝颗粒表面,制备了接枝微粒PGMA/(Al)_2O_3。考察了各种因素对接枝率的影响;利用红外光谱、扫描电镜表征了PGMA/(Al)_2O_3;并通过扫描电镜观察了PGMA/(Al)_2O_3在环氧树脂中的分散情况,初步研究了PGMA/(Al)_2O_3对环氧树脂体系的增强增韧性能。结果表明:表面引发自由基聚合反应可以成功制备复合粒子PGMA/(Al)_2O3,其接枝率随引发剂浓度和氧化铝与GMA质量比的增大先增大后减小;将PGMA/(Al)_2O_3填充到环氧密封材料中后,氧化铝颗粒在环氧树脂中分散良好,其复合材料的韧性明显高于未改性Al2O3填充的复合材料。 相似文献
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从性能,组织结构以及应用情况等方面介绍了Al2O3基陶瓷刀具的研究现状,并对其增韧机制进行了概述。 相似文献
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本工作以改善纳米粒子在环氧树脂基体中的分散性,提高无机粒子与基体的界面结合力为目的,选择了硅烷偶联剂KH550和KH570分别对纳米Al2O3粒予表面进行改性。文章系统研究了各种聚合条件(加料顺序、偶联剂加入量、反应时间)对改性效果的影响。TGA测试表明获得了不同接枝率的改性粒子。改性粒子与环氧树脂反应后进行的TGA测试以及FTIR测试证明了KH550改性的纳米粒子能够与环氧树脂发生反应,而KH570改性的纳米粒子不能发生反应。 相似文献
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为了减少石墨材料的高温氧化消耗,以普通石墨电极为例,设计并制备了氧化铝抗氧化涂层。采用氧化失重分析法对有涂层和无涂层石墨电极进行了对比研究,发现有涂层石墨电极的氧化失重率明显低于无涂层石墨电极。同时采用扫描电镜对涂层的形貌进行观察。研究结果表明:自行研制的氧化铝涂层具有很好的高温抗氧化性能。 相似文献
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In this article, two kinds of methods for grafting polyglycidyl methacrylate (PGMA) onto Al2O3 surface by the radical polymerization initiated by peroxide groups and double bond groups, respectively, were investigated. In the first method, peroxide groups, as initiators, were immobilized onto the Al2O3 surface. Then, GMA was polymerized on Al2O3 under the radicals decomposed by peroxide groups, and PGMA was grafted onto Al2O3. But in the second method, 3‐methacryloylpropyl trimethoxysilane was chemically bonded onto the Al2O3 surfaces firstly to introduce double bonds. Secondly, the copolymerizations between the immobilized double bonds and the monomer GMA were performed, homopolymerizations of GMA followed, and finally PGMA was grafted to the Al2O3 surfaces. The effects of grafting methods on grafting degree were examined mainly. At the same time, the effects of different grafting conditions on the grafting degree were researched. Furthermore, the effect of the grafted particles PGMA/Al2O3 on impact strength of the epoxy composites was studied. It was found that the grafting degree achieved by the first method was much higher than that by the second, and the grafting degree can reach about 54%. Moreover, the impact strength of epoxy composites containing PGMA/Al2O3 particles were improved largely, and which increased with the grafting degree. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 相似文献
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Effect on the toughness and adhesion properties of epoxy resin modified with silyl-crosslinked urethane microsphere 总被引:1,自引:0,他引:1
In order to give a toughness and improve adhesion properties of the cured epoxy system, modified epoxy resins, which have pre-reacted urethane microspheres formed using dynamic vulcanization method in liquid diglycidylether of bisphenol A, were prepared. It was found that the size of the particles decreased to sub-micro order with increase in solubility of urethane oligomers in epoxy resin, and coefficient of variance in the particle size distribution resulted in less than 15%. Fracture energy G1c of the cured system was highly improved. Lap shear strength and peel strength were also improved. These mechanical and adhesion properties do not depend on any curing condition of epoxy resin because of the existing stable particles in the epoxy resin before curing. 相似文献
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采用悬浮聚合的方法,以过氧化苯甲酰为引发剂,制备了不饱和聚酯(UP)/A l2O3复合微粒,考察了分散剂用量、分散助剂、油水比、搅拌速度等工艺条件对复合微粒平均粒径、粒径分布、均方偏差及其目标粒径质量分率的影响,测定了复合微粒的硬度。得到UP/A l2O3复合微粒悬浮聚合的最佳配方及工艺为UP 100份、A l2O355份、羟基磷酸钙0.5份、聚乙烯醇8份、NaC l 1.6份、过氧化苯甲酰1.0份、十二烷基苯磺酸钠0.3份、油水比1∶4、反应温度85℃和搅拌速度600 r/m in。制备出圆整光滑的复合微粒磨料,目标微粒的质量分率达到59.14%。 相似文献
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本文从纳米结构喂料制备、纳米Al2O3-TiO2涂层结构特征及其形成机制、喷涂工艺及在线控制、纳米Al2O3-TiO2涂层性能4个方面论述了等离子喷涂纳米Al2O3-TiO2涂层的研究进展。在此基础上,对等离子喷涂纳米Al2O3-TiO2涂层的前景进行了展望。 相似文献
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纳米ZrO2对Al2O3陶瓷性能的影响 总被引:5,自引:0,他引:5
以纳米ZrO2,微米Al2O3为原料,采用无压烧结方式制备了ZTA复相陶瓷.结果表明:纳米ZrO2的加入有利于制备细晶ZTA复相陶瓷.此外,nano-ZrO2的加入对Al2O3陶瓷的显微结构也产生影响,ZrO2颗粒以"晶内型"和晶界型2种形式存在.合理的配方组成及制备工艺有利于ZrO2以四方亚稳相存在.ZrO2质量分数为30%时,其四方相质量分数可达69%,有利于应力诱导相变增韧,该ZTA复相陶瓷的抗弯强度、断裂韧性分别达到604MPa,6.87MPa·m1/2. 相似文献