共查询到19条相似文献,搜索用时 127 毫秒
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以减三糠醛抽出油为相容剂,90#沥青为基质沥青,LG501S为改性剂,考察了相容剂的不同掺入量(占基质沥青质量)0,1.0%,2.0%,3.0%,4.0%,5.0%对改性沥青性能的影响,分析了增加相容剂掺入量沥青相与SBS相的形态特征。结果表明,增加相容剂掺入量后,改性沥青针入度、弹性恢复逐渐升高,软化点、针入度比逐渐降低,经过旋转薄膜烤箱(RTFOT)后,改性沥青5℃延度、5℃老化后延度逐渐增加,提高了改性沥青的延伸性能。随着相容剂掺入量的增加,改性沥青的高温抗车辙因子能力降低,低温抗裂性能提高;改性剂SBS在沥青中的粒径逐渐减小,分布律逐渐增加,使改性沥青的储存稳定性得到显著提高。 相似文献
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采用聚烯烃弹性体(POE)对苯乙烯-丁二烯-苯乙烯嵌段共聚物(SBS)改性沥青进行复配改性,制备了POE/SBS改性沥青混合料。考察了POE用量对SBS改性沥青抗老化性能的影响。结果表明,POE/SBS复配改性能提升沥青混合料的高温抗老化性能,且对低温性能有一定的改善效果。POE改善了SBS改性沥青混合料的抗车辙和抗老化性能,但会在一定程度上降低其低温韧性。当在沥青中加入质量分数分别为4%和3%的SBS和POE,POE/SBS改性沥青混合料的综合性能较佳。 相似文献
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SBS改性沥青化学交联过程的微观结构和性能研究 总被引:2,自引:0,他引:2
研究了SBS改性沥青在反应性改性过程中的微观相态结构变化,以及交联剂对改性沥青性能的影响.结果表明:化学交联反应可以改变石油沥青的胶体结构,从而显著改善改性沥青的储存稳定性、高温稳定性和感温性;反应性改性沥青的微观相态结构不但与聚合物的品种有关,也与基质沥青的化学组成密切相关,在高速剪切过程中逐渐由沥青为连续相、聚合物为分散相的"海""岛"型结构,转变为聚合物相和沥青相互相贯穿网络的双连续相结构,SBS在高温储存过程中分散更加均匀,不发生离析现象. 相似文献
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With the increasing ratio of waste tire powder (WTP) to low‐density polyethylene (LDPE), the hardness and tensile strength of the WTP/LDPE blends decreased while the elongation at break increased. Five kinds of compatibilizers, such as maleic anhydride‐grafted polyethylene (PE‐g‐MA), maleic anhydride‐grafted ethylene‐octene copolymer (POE‐g‐MA), maleic anhydride‐grafted linear LDPE, maleic anhydride‐grafted ethylene vinyl‐acetate copolymer, and maleic anhydride‐grafted styrene‐ethylene‐butylene‐styrene, were incorporated to prepare WTP/LDPE blends, respectively. PE‐g‐MA and POE‐g‐MA reinforced the tensile stress and toughness of the blends. The toughness value of POE‐g‐MA incorporating blends was the highest, reached to 2032.3 MJ/m3, while that of the control was only 1402.9 MJ/m3. Therefore, POE‐g‐MA was selected as asphalt modifier. The toughness value reached to the highest level when the content of POE‐g‐MA was about 8%. Besides that the softening point of the modified asphalt would be higher than 60°C, whereas the content of WTP/LDPE blend was more than 5%, and the blends were mixed by stirring under the shearing speed of 3000 rpm for 20 min. Especially, when the blend content was 8.5%, the softening point arrived at 82°C, contributing to asphalt strength and elastic properties in a wide range of temperature. In addition, the swelling property of POE‐g‐MA/WTP/LDPE blend was better than that of the other compalibitizers, which indicated that POE‐g‐MA /WTP/LDPE blend was much compatible with asphalt. Also, the excellent compatibility would result in the good mechanical and processing properties of the modified asphalt. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011 相似文献
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Toughened polyoxymethylene by polyolefin elastomer and glycidyl methacrylate grafted high‐density polyethylene 下载免费PDF全文
Wenqing Yang Xuan‐Lun Wang Xingru Yan Zhanhu Guo 《Polymer Engineering and Science》2017,57(10):1119-1126
Ternary blends of polyoxymethylene (POM), polyolefin elastomer (POE), and glycidyl methacrylate grafted high density polyethylene (GMA‐g‐HDPE) with various component ratios were studied for their mechanical and thermal properties. The size of POE dispersed phase increased with increasing the elastomer content due to the observed agglomeration. The notched impact strength demonstrated a parabolic tendency with increasing the elastomer content and reached the peak value of 10.81 kJ/m2 when the elastomer addition was 7.5 wt%. The disappearance of epoxy functional groups in the POM/POE/GMA‐g‐HDPE blends indicated that GMA‐g‐HDPE reacted with the terminal hydroxyl groups of POM and formed a new graft copolymer. Higher thermal stability was observed in the modified POM. Both storage modulus and loss modulus decreased from dynamic mechanical analysis tests while the loss factor increased with increasing the elastomer content. GMA‐g‐HDPE showed good compatibility between the POM matrix and the POE dispersed phase due to the reactive compatibilization of the epoxy groups of GMA and the terminal hydroxyl groups of POM. A POM/POE blend without compatibilizer was researched for comparison, it was found that the properties of P‐7.5(POM/POE 92.5 wt%/7.5 wt%) were worse than those of the blend with the GMA‐g‐HDPE compatibilizer. POLYM. ENG. SCI., 57:1119–1126, 2017. © 2017 Society of Plastics Engineers 相似文献
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PA66/POE/POE-g-MAH的分散相形态与力学性能研究 总被引:3,自引:0,他引:3
以(乙烯/辛烯)共聚物(POE)和马来酸酐接枝POE(POE-g-MAH)并用,制备了尼龙(PA)66/POE/POE-g-MAH合金,研究了POE-g-MAH用量对合金形态结构、力学性能的影响.结果表明,随着POE-g-MAH含量的增加,PA66/POE/POE-g-MAH合金的形态结构得到明显改善,弹性体分散相粒径细化且分布均匀,冲击强度显著提高;分散相粒径越小,粒径分布越均匀,POE-g-MAH较好增韧PA66的粒径范围是0.1~0.3μm;弹性体含量一定时,合金的缺口冲击强度随弹性体的细化而增大,但拉伸屈服强度和拉伸弹性模量不受影响. 相似文献
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DCP用量对动态硫化POE/PP热塑性弹性体性能的影响 总被引:1,自引:0,他引:1
研究了过氧化二异丙苯(DCP)用量对动态硫化乙烯一辛烯共聚物聚丙烯(POE/PP)体系的物理性能以及PP结晶形态和POE相态结构的影响。结果表明:随DCP用量的增加,POE/PP体系的交联密度增大,而断裂伸长率、永久变形和拉伸强度下降。过量DCP的加人会导致PP降解,使体系的熔体流动速率随DCP用量的增加呈上升趋势。DSC分析表明,随着DCP用量的增加,POE/PP体系结晶度下降。微观分析得出,DCP对POE/PP体系相态结构影响显著,当DCP用量为1份时交联POE以较小的颗粒均匀分布于PP连续相中。 相似文献
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Jingbo Hu Changqing Fang Shisheng Zhou Linna Jiao Maorong Zhang Di Wu 《乙烯基与添加剂工艺杂志》2015,21(3):215-219
Waste‐polyethylene (WPE) in packaging, instead of virgin polymer, was utilized as a modifier of base asphalt, and rheological properties of the modified asphalt were studied. Results show that the modified asphalt possesses better anti‐distortion capacity than the base asphalt, as indicated by the fact that the modified asphalt has higher viscosity and smaller endothermic peak dispersion in the transformation process of asphalt aggregation. Compared with base asphalt, the modified asphalt has higher complex modulus (G*), storage modulus (G′), and dissipation modulus (G″). In addition, the modified asphalt has smaller phase angle (δ), less tangent (tanδ), and lower rut factor (G*/sinδ), reflecting the high‐temperature rut resistance of the asphalt. The improvement of the rheological properties is related to the main features of the modified asphalt, including the swelling, whereas packaging‐waste‐PE absorbs low‐molecular‐weight fractions of asphalt, the displacement restriction of asphalt particles, and the molecular structure and performance of PE molecules. J. VINYL ADDIT. TECHNOL., 21:215–219, 2015. © 2014 Society of Plastics Engineers 相似文献
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