On the entanglement-based mechanism in thermal degradation of vinyl polymers

被引:7
作者
Sawaguchi, Takashi [1 ]
Sasaki, Daisuke [2 ]
Takamura, Atsushi [2 ]
机构
[1] XTEX Corp, Konan Ku, X, 5-48-7 Serigaya, Yokohama, Kanagawa 2330006, Japan
[2] San Ei Kogyo Corp, 5-4-19-206A, Kashiwa, Chiba 2770882, Japan
关键词
Entanglement; Unentanglement; Reaction field; Constraint release; Thermal degradation; Vinyl polymer; SELF-DIFFUSION COEFFICIENT; MOLECULAR-WEIGHT; VOLATILE OLIGOMERS; LINEAR POLYSTYRENE; POLYISOBUTYLENE; MELT; VISCOSITY; PYROLYSIS; DENSITY;
D O I
10.1016/j.polymdegradstab.2019.108990
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
In thermal degradation of the main-chain-scission type of vinyl polymers as a polymer reaction in melt, we propose that each subsequent elementary reaction of terminal macroradicals generated by the initiation is significantly influenced by entanglement constraint of molten polymer chain which is a reaction field. First, the intermolecular hydrogen abstraction followed by beta-scission occurs dominantly at other molecules forming the entanglement constraint tube. As a result, the reaction field becomes rapidly drop in the molecular weight M of molten polymer to the region of M< M-c (characteristic molecular weight) and furthermore M < M-e (entanglement molecular weight). Thus, in the reaction field constituted by isolated random coil chain that the entanglement is disentangled and entanglement constraint is released, the intramolecular hydrogen abstraction occurs predominantly because it is controlled by the activation energy and the frequency factor. On the other hand, the direct beta-scission (depolymerization) of the macroradicals also takes place in tubes independent of entanglement constraints. (C) 2019 Elsevier Ltd. All rights reserved.
引用
收藏
页数:7
相关论文
共 50 条
  • [31] Thermal Degradation Kinetics of Poly (vinyl chloride)
    Han, Bin
    Wu, Yulong
    Rui, Guo
    Feng, Wei
    Chen, Zhen
    Yang, Mingde
    ADVANCE IN ECOLOGICAL ENVIRONMENT FUNCTIONAL MATERIALS AND ION INDUSTRY, 2010, 96 : 245 - +
  • [32] Thermal degradation of copolymers of acrylonitrile, methacrylonitrile and vinylidene cyanide with vinyl acetate
    Laleque-Mignard, N
    Montheard, JP
    Boinon, B
    JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS, 1998, 47 (02) : 145 - 164
  • [33] Advantages and limitations of channel multiplexing for discrete-variable entanglement-based quantum key distribution
    Maiti, Indranil
    Lasota, Mikolaj
    NEW JOURNAL OF PHYSICS, 2025, 27 (03):
  • [34] Thermal degradation kinetics of vinyl polyperoxide copolymers
    Sivalingam, G
    De, P
    Karthik, R
    Madras, G
    POLYMER DEGRADATION AND STABILITY, 2004, 84 (01) : 173 - 179
  • [35] Kinetic Parameters of Thermal Degradation of Polymers
    朱新生
    程嘉祺
    Journal of Donghua University(English Edition), 2003, (01) : 54 - 57
  • [36] Ferrocene based ionic liquid: synthesis, structure, transport properties and mechanism of thermal degradation
    Arkhipova, Ekaterina A. A.
    Ivanov, Anton S. S.
    Maslakov, Konstantin I. I.
    Kupreenko, Stepan Yu. M.
    Levin, Mikhail A.
    Iurenkov, Maksim V. M.
    Lyssenko, Konstantin A.
    Savilov, Serguei V.
    Aldoshin, Sergey M.
    JOURNAL OF MOLECULAR LIQUIDS, 2022, 355
  • [37] The effect of carbon black on the thermal decomposition of vinyl polymers
    Jakab, E
    Blazsó, M
    JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS, 2002, 64 (02) : 263 - 277
  • [38] Thermal decomposition of mixtures of vinyl polymers and lignocellulosic materials
    Jakab, E
    Blazsó, M
    Faix, O
    JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS, 2001, 58 (58-59) : 49 - 62
  • [39] Mechanism of thermal degradation of polyester fibre in a furnace pyrolyzer
    Zvanskii, BV
    Krasev, SY
    Koren, AO
    FIBRE CHEMISTRY, 1997, 29 (06) : 363 - 366
  • [40] Mechanism of thermal degradation of polyester fibre in a furnace pyrolyzer
    B. V. Zvanskii
    S. Yu. Krasev
    A. O. Koren'
    Fibre Chemistry, 1997, 29 : 363 - 366