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PEB-g-MAN增韧SAN树脂的力学性能及增韧机理的研究 被引量:2

Toughening Effect of PEB-g-MAN on SAN Resin and Its Toughening Mechanism
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摘要 用悬浮接枝共聚合法合成了乙烯/1-丁烯共聚物(PEB)与甲基丙烯酸甲酯(MMA)/N烯腈(AN)的接枝共聚物(PEB-g-MAN),并用其增韧苯乙烯/丙烯腈共聚物(SAN)。研究了SAN/PEPrg-MAN共混物的力学性能、增韧机理和相结构。结果表明:PEB-g-MAN是SAN树脂的优良增韧剂,当PEB用量为25%时,SAN/PEB-g-MAN的缺口冲击强度达63.3kJ/m^2,约为SAN树脂的60倍。SAN/PEB-g-MAN共混物在PEB含量为15%~20%时发生脆韧转变。脆韧转变前、脆韧转变过程中和脆韧转变后的冲击断面形态的SEM分析表明,共混物的增韧机理先是裂纹支化终止和空穴化,随后为高度空穴化,再为基体剪切屈服兼空穴化,最后转变为空穴化为主,剪切屈服为辅。TEM分析表明,PEB均匀分散于SAN连续相中,两相界面模糊,具有良好的相容性,且随着PEB含量的增加,共混物的相结构由“海-岛”结构转变为“双连续相”结构。 PEB-g-MAN, synthesized by suspension grafting copolymerization of methyl methacrylate and acrylonitrile onto PEB, was blended with styrene-acrylonitrile copolymer (SAN). The mechanical properties, phase structure, and toughening mechanism of the SAN/PEB-g-MAN blends were studied using SEM and TEM. The notched impact strength of the blends (25%PEB) reached 63.3 kJ/m^2, which was nearly 60 times that of neat SAN. When the content of PEB was between 15 %~20 %, a brittle ductile transition was observed. TEM and SEM showed that SAN/ PEB-g-MAN were partially compatible. When the PEB content was low, the toughening mechanism of the blends was crack branching and termination with slight cavitation. As the PEB content increasing, the toughening mechanism shifted to extensive cavitation, and further to shear yielding accompanied by cavitation.
出处 《中国塑料》 CAS CSCD 北大核心 2009年第10期40-44,共5页 China Plastics
关键词 乙烯/1-丁烯共聚物和甲基丙烯酸甲酯/丙烯腈的接枝共聚物 苯乙烯/丙烯腈共聚物 增韧机理 相结构 脆韧转变 poly (ethylene-co-l-butene)-graft-methyl methacrylate-acrylonitrile styreneacryloni-trile copolymer toughening mechanism phase structure brittle-ductile transition
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参考文献17

  • 1Roland H. Horst, H. Henning Winter. Stable Critical Gels of A Crystallizing Copolymer of Ethene and 1-Butene [J]. Macromolecules, 2000, 33(1) :130-136.
  • 2张启兴,王海华,梁忠辉,欧阳巍,伍青,卢泽俭.Ti系高效催化剂乙烯-1-丁烯气相共聚反应及共聚物结构与性能[J].高分子材料科学与工程,1997,13(6):60-66. 被引量:5
  • 3Van Grieken R. , Martin C. , Moreno J. , et al. Ethylene/ 1-Butene Copolymerization over Heterogeneous Metallocene Catalyst [J]. Macromolecular Symposia, 2007, 259 (1) :174-180.
  • 4Mader D. , Thomann Y. , Suhm J. , et al. Influence of Comonomer Incorporation on Morphology and Thermal and Mechanical Properties of Blends based upon Isotactic Metallocene-polypropene and Random Ethene/1-Butene Copolymers [J].Journal Applied Polymer Science, 1999, 74(4): 838-848.
  • 5D. E. Mouzakis, D. Mader, R. Mulhaupt, et al. Relationship between Morphology and Mechanical Properties of Polypropylene/Ethene-co-butene Binary Blends with Various Butene Contents[J]. Journal of Materials Science, 2000,35(3) :1 219-1 230.
  • 6Park K. W., Chowdhury S. R., Park C. C., et al. Effect of Dispersion State of Organoclay on Cellular Foam Structure and Mechanical Properties of Ethylene Vinyl Acetate Copolymer/Ethylene-l-butene Copolymer/ Organoclay Nanocomposite Foams[J]. Journal Applied Polymer Science, 2007,104 (6):3 879-3 885.
  • 7Dai J. Q. , Wang L. S. , Cai T. M. , et al. EPDM/St-AN Graft Copolymerization Reaction Behavior by Phase Inversion Emulsion and the Toughness Effect of EPDM-g-SAN on SAN Resin[J]. Journal of Applied Polymer Science, 2007, 107(5): 3 393-3 400.
  • 8Bai S. L. , Wang G. T. , Hiver J. M. , et al. Microstructures and Mechanical Properties of Polypropylene/Polyamide 6/Polyethelene-octene Elastomer Blends [J]. Polymer, 2004, 45(9): 3 063-3 071.
  • 9WuC. S., Lai S. M., Liao H. T.. Graft Reaction of Acrylic Acid onto Metalloeene-based Polyethylene-octene Elastomer[J]. J. Appl. Poly. Sci. , 2002,85 (14): 2 905-2 912.
  • 10LuM. F., ZhangS. J., YuD. S.. Study onPolypropylene/Ammonium Polyphosphate Composites Modified by Ethylene-1-octene Copolymer Grafted with Glycidyl Methacrylate[J]. J. Appl. Poly. Sci., 2004, 93(1):412- 419.

二级参考文献39

  • 1张启兴,卢泽俭,欧阳巍,伍青,王海华.Ti-Mg催化剂的预聚合及其对乙烯气相聚合的影响[J].合成树脂及塑料,1994,11(3):8-14. 被引量:6
  • 2代惊奇,王炼石,蔡彤旻,张安强,曾祥斌.相反转乳液接枝法合成EPDM-g-SAN及其对SAN树脂的增韧作用[J].橡胶工业,2007,54(3):150-153. 被引量:6
  • 3马德柱,何平笙,徐种德,等.高聚物的结构与性能(第二版)[M].北京:科学出版社,2003.161-164.
  • 4Wagner E R, Robeson L M. Impact Polystyrene: Factors Controlling the Rubber Efficiency [J]. Rubber Chemistry and Technology, 1970, 43(5): 1129-1137.
  • 5Manson J A, Sperling L H. Polymer Blends and Composites. Chapter 3, Plenum press, New York, 1976.
  • 6马洵炜.改性复合阻燃剂对HIPS的增韧阻燃作用[A]硕士学位论文.广州华南理工大学,2003-06.
  • 7Cigna G, Lomellini P, Merlotti M J. Impact Thermoplastics: Combined Role of Rubbery Phase Volume and Particle Size on Toughening Efficiency [J]. Appl Polymer Sci, 1989,37(6): 1527-1540.
  • 8Kinloch A J,Young R J. Fracture Behavious of Polymers.Applied Science Publishers Ltd. London and New York.1983:421-451.
  • 9Smith J A, Keskkula H. Sort-time Stress Relaxtion and Toughness of Rubber Modified Polystyrene [J]. J Appl Polym Sci. 1960,3(8): 132-142.
  • 10Bucknall C B, Smith R R. Stress-whitenig in High Impact Polystyrene[J]. Polymer, 1965, 6(8): 437-446.

共引文献27

同被引文献38

  • 1蔡世绵,涂建军,汪复.乙烯与1-丁烯共聚合的研究[J].石油化工,1994,23(12):776-782. 被引量:5
  • 2张学全,陈辉,黄葆同,杨永然,姜明,王展望,张俊杰.MgCl_2·EB/TiCl_4高效载体催化剂的乙烯/1-丁烯共聚反应研究[J].石油化工,1994,23(5):286-289. 被引量:4
  • 3沈勇,王炼石,张安强.PBA-g-SAN的表征及其对SAN树脂的增韧作用[J].弹性体,2007,17(2):37-41. 被引量:4
  • 4van Grieken R., Martin C., Moreno J., Prieto O., Bravo J. M.. Macromolecular Symposia[J], 2007, 259: 174-180.
  • 5SUNBai-Ping(孙佰平).化学工程,2007,.
  • 6Thomann Y., Suhm J, Thomann R., Bar G., Maier R. D., Muhlaupt R.. Macromolecules[J]..1998, 31:5441-5449.
  • 7Thomann Y., Suhm J, Thomann R., Maier R. D., Mulhaupt R., Bar G.. Macromolecular Symposia[J]..2000, 149(1):125-130.
  • 8Mader D., Thomann Y., Suhm J., Mulhaupt R.. Journal of Applied Polymer Science[J], 1999, 74(4): 838-848.
  • 9Mouzakis D. E., Mader D, Mulhaupt R., Karger-Kocsis J.. Journal of Materials Science[J]..2000, 35:1219-1230.
  • 10Park K. W., Chowdhury S. R., Park C. C., Kim G. H.. Journal of Applied Polymer Science[J], 2007, 104(6): 3879-3885.

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