Competition between α, β, and γ polymorphs in β-nucleated metallocenic isotactic polypropylene

被引:175
作者
Krache, Rachida
Benavente, Rosario
Lopez-Majada, Juan M.
Perena, Jose M.
Cerrada, Maria L.
Perez, Ernesto [1 ]
机构
[1] Univ Ferhat Abbes, Fac Sci Ingn, Dept Genie Proc, LMPM, Setif 19000, Algeria
[2] CSIC, Inst Ciencia & Tecnol Polimeros, E-28006 Madrid, Spain
关键词
D O I
10.1021/ma0710636
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The competition between alpha, beta and gamma polymorphs has been studied in a P-nucleated metallocenic isotactic polypropylene, iPP, as a function of the cooling rate and of the isothermal crystallization temperature, by performing X-ray diffraction and DSC experiments. It was found that the addition of a 1% by weight of a typical P-nucleating agent is not enough to develop any appreciable amount of beta modification, at least under the crystallization conditions used, which cover a wide range of cooling rates. In comparison, the same amount of nucleating agent added to a Ziegler-Natta iPP leads to almost 100% of beta form at low cooling rates. It seems that such amount of beta nucleating agent is not enough to counterbalance the well-known gamma nucleation ability of the relatively high content of defects (stereo- and regioerrors) which are present in the studied metallocenic iPP, and only different proportions of gamma and a modifications are obtained in this sample, the relative amount of them depending on the cooling rate. On the contrary, if a 5% nucleating agent is added, the beta modification is also obtained, in addition to the gamma and alpha polymorphs. However, now the amount of beta crystals as a function of the cooling rate follows a trend opposite to that for the Ziegler-Natta iPP: the higher are the cooling rates (or the lower are the isothermal crystallization temperatures) the larger proportions of beta modification are obtained. It is deduced, therefore, that the nucleation ability of the chain errors which leads to the development of the gamma form predominates over that one of the nucleating agent. The enthalpies for the 100% crystalline modifications, estimated from the enthalpies of melting and from the X-ray determined proportions of the different polymorphs, are rather similar: 162, 159, and 158 J/g for the alpha, beta and gamma phases, respectively. These values are inside the experimental error.
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页码:6871 / 6878
页数:8
相关论文
共 48 条
  • [1] POLYMORPHISM OF CRYSTALLINE POLYPROPYLENE
    ADDINK, EJ
    BEINTEMA, J
    [J]. POLYMER, 1961, 2 (02) : 185 - 193
  • [2] Structural and kinetic factors governing the formation of the γ polymorph of isotactic polypropylene
    Alamo, RG
    Kim, MH
    Galante, MJ
    Isasi, JR
    Mandelkern, L
    [J]. MACROMOLECULES, 1999, 32 (12) : 4050 - 4064
  • [3] Structure and mechanical behavior of the mesomorphic form in a propylene-b-poly(ethylene-co-propylene) copolymer and its comparison with other thermal treatments
    Arranz-Andrés, J
    Benavente, R
    Pérez, E
    Cerrada, ML
    [J]. POLYMER JOURNAL, 2003, 35 (10) : 766 - 777
  • [4] Bond EB, 1999, J POLYM SCI POL PHYS, V37, P3050, DOI 10.1002/(SICI)1099-0488(19991101)37:21<3050::AID-POLB14>3.0.CO
  • [5] 2-L
  • [6] BRUCKNER S, 1989, NATURE, V340, P455, DOI 10.1038/340455a0
  • [7] POLYMORPHISM IN ISOTACTIC POLYPROPYLENE
    BRUCKNER, S
    MEILLE, SV
    PETRACCONE, V
    PIROZZI, B
    [J]. PROGRESS IN POLYMER SCIENCE, 1991, 16 (2-3) : 361 - 404
  • [8] On the crystallization of gamma-isotactic polypropylene: A high pressure study
    Bruckner, S
    Phillips, PJ
    Mezghani, K
    Meille, SV
    [J]. MACROMOLECULAR RAPID COMMUNICATIONS, 1997, 18 (01) : 1 - 7
  • [9] Tailoring of the α-, β-, and γ-modification in isotactic polypropene and propene/ethene random copolymers
    Busse, K
    Kressler, J
    Maier, RD
    Scherble, J
    [J]. MACROMOLECULES, 2000, 33 (23) : 8775 - 8780
  • [10] CORRADINI P, 1989, POLYM COMMUN, V30, P281