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杨军

作品数:11 被引量:156H指数:7
供职机构:中国科学院长春应用化学研究所更多>>
发文基金:国家自然科学基金国家重点基础研究发展计划更多>>
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11 条 记 录,以下是 1-10
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HIPS/PP熔融反应共混及其动态力学性质被引量:6
1998年
研究了高抗冲聚苯乙烯(HIPS)/聚丙烯(PP)共混物在过氧化二异丙苯(DCP)存在下的熔融反应过程及其动态力学性质.HIPS在DCP存在下以聚苯乙烯(PS)的降解为主,伴随着聚丁二烯(PB)的交联和接枝,PP在DCP存在下以降解为主,HIPS/PP在DCP存在下以PP同HIPS的反应接枝为主,这种原位生成的增容剂显著地改善了HIPS/PP两组份间的相容性,其分子运动特征较前两者发生明显变化,PS的Tg下降,PB和PP的Tg升高.
刘万军杨军刘景江
关键词:高抗冲反应增容熔融共混物
HIPS/MA接技共聚物对HIPS/PA1010共混体系的增容被引量:2
1998年
制备了高抗冲聚苯乙烯和马来酸酐的接枝共聚物,利用红外光谱,电子能谱和动态力学谱对产物的结构进行了表征,并通过滴定法测定了接枝物中马来酸酐的含量。结果表明马来酸酐接枝到了高抗冲聚苯乙烯中顺丁橡胶的分子链上,接技率为4.7%。研究了该接枝共聚物对PA1010/HIPS共混物的增容作用。电镜照片显示,随着共聚物中接枝物含量的增加,分散相相区尺寸明显减小,说明增容效果显著。测定了共混体系的拉伸行为,研究了拉伸断面形貌,结果显示增容剂的加入提高了共混物的力学性能。
陈广新杨军刘景江
关键词:高抗冲聚苯乙烯
超细碳酸钙填充聚丙烯的拉伸和结晶行为的研究被引量:36
2002年
研究了组成为 1phr和 10 phr的超细碳酸钙 (Ca CO3 ,0 .1μm)经偶联剂处理前后 ,填充聚丙烯(PP)的拉伸性能和结晶行为。结果表明 :Ca CO3 的加入增加了 PP的杨氏模量 (E) ,降低了 PP的断裂伸长率 (εb) ,1Phr样品与未填充 PP的 εb 的比值为 0 .5 6 ,10 phr时则迅速降至 0 .0 4。这一变化趋势明显不同于普通 Ca CO3 填充 PP所表现出来的行为。表面处理样品的 E和 εb 均大于相应组成的未经表面处理的样品 ,SEM照片显示偶联剂的作用改善了 Ca CO3 / PP的界面粘接性能。WAXD分析表明 ,Ca CO3 的加入提高了 PP的结晶度 ,结晶形态以 α晶为主 ,晶胞参数和微晶尺寸均有一定程度的变化。DSC结果表明 ,除了 CTUCPP- 10样品的过冷度降低以外 。
杨军刘万军陈广新刘景江
关键词:聚丙烯碳酸钙粉末超细粉
用仪器化冲击仪研究HIPS/SBS共混物的冲击性能被引量:5
1999年
用J-20型仪器化冲击仪研究了HIPS/SBS共混物在组成为100/0、100/5、100/10、100/15、100/20和100/25质量比下样品的Izod缺口冲击性能。结果表明,在组成范围内,随着SBS含量的增加,样品的Izod缺口冲击强度随之增加。质量比为100/25样品的Izod缺口冲击强度值(225.9J/m)比质量比为100/0的样品(108.7J/m)增加了1倍以上。通过对冲击断裂过程的分析表明,冲击强度的提高主要是由于缺口根部应力集中产生塑性区所消耗的裂纹引发能的提高引起的。
杨军刘景江
关键词:冲击韧性仪器化HIPSSBS共混物
弹性体改性高抗冲聚苯乙烯的力学行为Ⅰ.拉伸和动态力学性能被引量:14
1995年
研究了高抗冲聚苯乙烯(HIPS)同苯乙烯-丁二烯-苯乙烯热塑性弹性体(SBS)、丁苯橡胶(SBR)、高顺式聚丁二烯橡胶(PBR)共混物的拉伸性能及动态力学性质。SBS改性的HIPS试样具有最大的断裂能,最大的断裂伸长率,较高的拉伸杨氏模量、屈服强度,屈服点过后有明显的应变硬化现象。SBR改性的HIPS也呈现韧性断裂,拉伸过程中有明显的应力发白现象。PBR改性HIPS试样表现为脆性断裂,力学性能变劣,3种改性试样的动态力学性能谱同HIPS相比均发生明显变化,表明分子运动的特征发生改变。
杨军刘景江
关键词:聚苯乙烯动态力学性能共聚物
高抗冲聚苯乙烯的增韧机理被引量:32
1997年
概述了以高抗冲聚苯乙烯(HIPS)为中心的有关橡胶增韧机理的理论,并且总结了界面性能、粒子尺寸、粒子间距及缠结密度等因素对橡胶/高分子共混体系性能的影响。
杨军刘万军刘景江
关键词:橡胶增韧机理共混体系聚苯乙烯高抗冲
高抗冲聚苯乙烯的增韧机理和断裂力学
杨军
关键词:聚苯乙烯增韧机理
高抗冲聚苯乙烯中银纹的引发与终止被引量:7
2000年
Initiation and termination of crazes in high impact polystyrene (HIPS) were studied by transmission electron microscope. Instead of the first initiation of crazes in the vicinity of the equator or rubber particles, ribbon\|shaped crazes beyond the region were observed on the TEM photos. The starting point and the end point of each ribbon were noticed not to be randomly located on the surface of the cellar particles in HIPS. The spots connecting to the ligaments between the PS rigid inclusions in the cellar particle are found to be the locations where crazes were initiated and terminated preferentially. In addition, the crazes generated at those spots were much thicker and longer. The thoughness of high impact polystyrene was enhanced by the multiple crazes formed in the matrices, through the reduction of the craze stress at room temperature with increasing the volume fraction of polybutadiene at these spots in the dispersed phase. These results conducted that not only the cell structure of the domains in HIPS was not homogeneous but also the polybutadiene ligaments between PS rigid inclusions in the domains were inhomogeneous. Therefore, the responsibility of those polybutadiene ligaments with different thickness to the stresses was different and it forced the crazing initiation and growing preferentially. The crazes were created in some regions in the matrices; On the contrary, rare crazes were formed in the other regions in spite of these regions surrounded around the same dispersed particles. The relation between the spots on the surface and the inner structure of the cellar particle was discussed in this paper.
杨军刘景江
关键词:高抗冲聚苯乙烯银纹橡胶增韧机理
超细CaCO_3的粒子尺寸对PP结晶行为的影响被引量:48
2001年
The effects of CaCO\-3 on the crystallization behavior of polypropylene (PP) were studied by means of DSC and WAXD.The average sizes of the CaCO\-3 powders used were 0\^1?μm (UC) and 0\^5?μm (GC),respectively.The PP/CaCO\-3 composites at compositions of 1?phr and 10 phr were investigated.The results showed that the addition of CaCO\-3 reduced the supercooling,the rate of nucleation and the overall rate of crystallization (except for the 10?phr UC/PP sample).The crystallinity of PP was increased and the size distribution of the crystallites of α \|PP was broadened.On the other hand,the crystallization rate of 10?phr UC/PP is 1\^5 times higher than that of neat PP.It has an overall rate of crystallization 2 times as much as that of the neat PP and has the maximum crystallinity.The sizes of crystallites and the unit cell parameters of α \|PP were varied by the addition of CaCO\-3. β \|PP was formed by addition of GC and was not detected by addition of UC.The differences of crystallization behaviors of PP might be attributed to the combined effects of the content and size of CaCO\-3 filled.
杨军刘万军陈广新刘景江
关键词:聚丙烯碳酸钙超细粉末粒子尺寸复合材料
用SBS或SBR或BR改进HIPS的冲击性能被引量:11
1995年
采用机械共混法,在弹性体用量为5%~25%时,研究了SBS,SBR,BR分别对HIPS的增韧效果。SBS可使HIPS的冲击韧性大幅度提高,并随SBS含量增加显著上升。SBR也能提高HIPS的冲击韧性,但幅度不大。BR的加入使HIPS的冲击韧性下降。前两者的冲击试样断面平整而光洁,有明显的应力发白现象,属韧性断裂,后者的断面粗糙不平,无应力发白现象,属脆性断裂。改性HPS的形态随着弹性体的不同以及含量的变化均有不同特点,与冲击韧性的变化相对应。
杨军刘景江
关键词:橡胶增韧塑料丁苯橡胶
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