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首页> 外文期刊>Journal of Materials Science >Investigation on terpolymer of ethylene/propylene/omega-bromo-alpha-olefins catalyzed by titanium complexes
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Investigation on terpolymer of ethylene/propylene/omega-bromo-alpha-olefins catalyzed by titanium complexes

机译:钛配合物催化乙烯/丙烯/欧米茄 - 溴-α-烯烃三元共聚物的研究

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摘要

Polyolefins with polar groups exhibited many applications as high-performance materials have been the subject of considerable research. In this study, terpolymers of omega-bromo-alpha-olefins with ethylene and propylene were synthesized in the presence of three multi-chelated non-metallocene titanium complexes. The structure and properties of the terpolymers were determined by H-1 NMR, C-13 NMR, Fourier transform infrared, differential scanning calorimetry after treatment by successive self-nucleating and annealing and wide-angle X-ray diffractograms. Furthermore, the stress-strain behaviors of the terpolymers were measured with ASTMD1708 microtensile, and the specimens were from the obtained terpolymer films. The results indicated that these catalysts were efficient for the terpolymerization. The catalytic activity was as high as 6.21 x 10(5) gP (molTi)(-1) h(-1) for terpolymerization of 11-bromo-1-undecylene with ethylene and propylene. The insertion ratio of 11-bromo-1-undecylene was up to 2.49 mol% confirmed by H-1 NMR and C-13 NMR. As for the terpolymers, their melting points decreased and their plasticity became weak with the incorporation of omega-bromo-alpha-olefins increasing. GPC results showed that the terpolymers had high weight-average molecular weight up to 2.51 x 10(5) g mol(-1). Molecular weight distribution of the terpolymers was about 2, implying single-site mechanism for the terpolymerization, but slightly broader than that of ethylene/propylene copolymer.
机译:具有极性基团的聚烯烃显示出许多应用,因为高性能材料一直是具有相当大的研究的主题。在该研究中,在三种多螯合的非茂金属钛配合物存在下合成具有乙烯和丙烯的ω-溴-α-烯烃的三元共聚物。通过连续自核和退火和广角X射线衍射图,通过H-1 NMR,C-13 NMR,C-13 NMR,C-13 NMR,傅立叶变换红外,差示扫描量热法测定三元共聚物的结构和性质。此外,用ASTMD1708微量调节测量三元共聚物的应力 - 应变行为,并从得到的三元共聚物膜中测量样品。结果表明,这些催化剂对于三聚合而有效。催化活性高达6.21×10(5)克(Molti)( - 1)H(-1),用于11-溴-1-不应亚亚亚亚亚丁烯与乙烯和丙烯。 11-溴-1-不应亚甲烯的插入率高达2.49mol%,通过H-1 NMR和C-13 NMR确认。至于三元共聚物,它们的熔点降低,并且它们随着ω-溴-α-烯烃的掺入而变弱。 GPC结果表明,三元共聚物的重量平均分子量高至2.51×10(5 )g摩尔(-1)。三元共聚物的分子量分布为约2,暗示三聚合的单点机制,但略宽于乙烯/丙烯共聚物的机制。

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  • 来源
    《Journal of Materials Science》 |2017年第10期|共11页
  • 作者单位

    Beijing Univ Chem Technol Coll Mat Sci &

    Engn State Key Lab Chem Resource Engn Key Lab Carbon Fiber &

    Funct Polymers Minist Educ Beijing 100029 Peoples R China;

    Beijing Univ Chem Technol Coll Mat Sci &

    Engn State Key Lab Chem Resource Engn Key Lab Carbon Fiber &

    Funct Polymers Minist Educ Beijing 100029 Peoples R China;

    Beijing Univ Chem Technol Coll Mat Sci &

    Engn State Key Lab Chem Resource Engn Key Lab Carbon Fiber &

    Funct Polymers Minist Educ Beijing 100029 Peoples R China;

    Beijing Univ Chem Technol Coll Mat Sci &

    Engn State Key Lab Chem Resource Engn Key Lab Carbon Fiber &

    Funct Polymers Minist Educ Beijing 100029 Peoples R China;

    Beijing Univ Chem Technol Coll Mat Sci &

    Engn State Key Lab Chem Resource Engn Key Lab Carbon Fiber &

    Funct Polymers Minist Educ Beijing 100029 Peoples R China;

    China Natl Petr Corp Liaoyang Petrochem Corp Liaoyang 111003 Peoples R China;

    China Natl Petr Corp Liaoyang Petrochem Corp Liaoyang 111003 Peoples R China;

    Beijing Univ Chem Technol Coll Mat Sci &

    Engn State Key Lab Chem Resource Engn Key Lab Carbon Fiber &

    Funct Polymers Minist Educ Beijing 100029 Peoples R China;

    Beijing Univ Chem Technol Coll Mat Sci &

    Engn State Key Lab Chem Resource Engn Key Lab Carbon Fiber &

    Funct Polymers Minist Educ Beijing 100029 Peoples R China;

    Beijing Univ Chem Technol Coll Mat Sci &

    Engn State Key Lab Chem Resource Engn Key Lab Carbon Fiber &

    Funct Polymers Minist Educ Beijing 100029 Peoples R China;

    Beijing Univ Chem Technol Coll Mat Sci &

    Engn State Key Lab Chem Resource Engn Key Lab Carbon Fiber &

    Funct Polymers Minist Educ Beijing 100029 Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 工程材料学;
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