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一种国产新型反应性增容剂在PA6与ABS合金中的应用 被引量:4

APPLICATION OF A HOMEMADE NOVEL COMPATIBILIZER IN PREPARING SUPER-TOUGHENING PA6/ABS BLENDS
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摘要 以国产苯乙烯-丙烯腈-顺丁烯二酸酐共聚物(SAM)为原位反应性增容剂,制备了超韧PA6/ABS合金。在m(PA6)/m(ABS)为50/50~70/30和SAM加入量为3%~4%时,23℃的合金悬臂梁缺口冲击强度达900J/m以上;-18℃的合金悬臂梁缺口冲击强度达270J/m。电镜和力学性能测试表明原位反应性增容使PA6和ABS两相界面张力降低,并使ABS分散颗粒变小及更均匀地分散于PA6中。另外,过多的SAM用量将导致PA6与SAM间的深度反应,使体系粘度上升和ABS相难于被分散。总之,SAM用量、相界面张力和ABS分散颗粒大小是影响该合金力学性能的关键因素。 The super-toughening PA6/ABS blends were successfully prepared using a homemade styrene-acrylonitrile-maleic anhydride terpolymer (SAM). The blends with the 50/50~70/30 mass ratios of PA6 to ABS and the addition of 3%~4% SAM exhibited the notched Izod strength>900 J/m at room temperature and >270 J/m at (-18) ℃. SEM photomicrographs and mechanical testing show that the in-situ reactive compatibilization with the addition of SAM makes the PA6/ABS interfacial tension reduced and ABS domains become smaller and more uniformly dispersed throughout the blends. The increase in SAM at above 7% limits the improvement in the properties of the blends, which is due to that the profound reaction between PA6 and SAM makes the blends more viscous and the dispersion of ABS domains difficult. Therefore, the size of ABS domains, the interfacial tension and amount of SAM play their important roles in improving the performance of PA6/ABS blends.
出处 《高分子材料科学与工程》 EI CAS CSCD 北大核心 2005年第2期264-266,270,共4页 Polymer Materials Science & Engineering
关键词 苯乙烯-丙烯腈-顺丁烯二酸酐共聚物 尼龙6 ABS 增容 超韧 聚合物合金 styrene-acrylonitrile-maleic anhydride terpolymer nylon 6 ABS compatibilization super-tough polymer alloy
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  • 1邱志勇,李松,张增民.PA/ABS塑料合金的研制[J].现代塑料加工应用,1996,8(1):1-5. 被引量:26
  • 2杉浦基之.-[J].工业材料,1991,39(15):39-45.
  • 3杉浦基这 森屋泰夫 等.-[J].工业材料,1990,38(17):17-23.
  • 4石正金 王荣伟 等.-[J].石油化工,2001,30:564-566.
  • 5Angola J C, Fujita Y, Sakai T, et al. J Polym Sci, Part B:Polym Phys, 1988, 26(4): 807-816.
  • 6Bruls W G M, Buntinx R A M, Reid V. Rubber-modifiedpolymer composition. Eur Pat Appl, EP 785 234. 1997.
  • 7Lavengood R E. Rubber-modified nylon composition. USA, US 4 777 211. 1988.
  • 8Aoki Y, Watanabe M. Impact resistant thermoplastic resin composition. USA, US 4 987 185. 1991.
  • 9Kudva R A, Keskkula H, Paul D R. Polymer, 2000, 41(1):225 -237.
  • 10Kudva R A, Keskkula H, Paul D R. Polymer, 2000, 41(1):239-258.

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  • 1李爱英,常杰云,王凯全,陆路德.PA6/ABS/ABS-g-MAH合金的研究[J].塑料工业,2005,33(B05):76-77. 被引量:10
  • 2王璐,郭宝华,谢续明.ABS的MAH/St多单体熔融接枝及其对PA6/ABS共混体系相形态和力学性能的影响[J].高分子学报,2005,15(2):213-218. 被引量:20
  • 3李超,李光吉,王志.超韧PA6/ABS合金的制备[J].塑料工业,2005,33(9):22-24. 被引量:14
  • 4蔡绪福,陈力,鲁成祥.ABS/PA6/SMA共混体系的结构与性能[J].四川大学学报(工程科学版),2005,37(6):81-86. 被引量:15
  • 5Paul D R, Bucknall C B. Polymer Blends. New York: John Wiley &Sons Ltd, 2000.83 - 118.
  • 6Scheirs J, Priddy D. Modem Styrenic Polymers: Polystyrenes and Styrenic Copolymers. West Sussex, England: John Wiley & Sons Ltd, 2003.3 - 24.
  • 7Fang Qinzhi, Wang Tiejun, Li Huimin. Large Tensile Deformation Behavior of PC/ABS Alloy. Polymer, 2006, 47 ( 14 ) : 5 174- 5 181.
  • 8Fang Qinzhi, Wang Tiejun, Li Huimin. 'Tail' Phenomenon and Fatigue Crack Propagation of PC/ABS Alloy. Polym Degrad Stab, 2008, 93(1): 281 - 290.
  • 9Steendam R, van Steenbergen M J, Hennink W E, et al. Effect of Molecular Weight and Glass Transition on Relaxation and Release Behaviour of Poly( DL-Lactic Acid) Tablets. J Controlled Release, 2001, 70(1 -2): 71 -82.
  • 10Ding Enyong, Cheng Rongshi. Novel Quasi-Isothermal Method of Measuring Heat Capacity in Temperature Modulated Differential Scanning Calorimetry. Thermochim Acta, 2001, 376(2) :133 - 139.

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