ICAR ATRP for Estimation of Intrinsic Macro-Activation/Deactivation Arrhenius Parameters under Polymerization Conditions

被引:30
作者
Porras, Carolina Toloza [1 ]
D'hooge, Dagmar R. [1 ]
Van Steenberge, Paul H. M. [1 ]
Reyniers, Marie-Francoise [1 ]
Marin, Guy B. [1 ]
机构
[1] Univ Ghent, Lab Chem Technol LCT, B-9052 Ghent, East Flanders, Belgium
关键词
TRANSFER RADICAL POLYMERIZATION; NITROXIDE MEDIATED POLYMERIZATION; DIFFUSION-CONTROLLED REACTIONS; ACTIVATION RATE CONSTANTS; N-BUTYL ACRYLATE; METHYL-METHACRYLATE; CHAIN TRANSFER; EQUILIBRIUM-CONSTANTS; RATE COEFFICIENTS; METALLIC COPPER;
D O I
10.1021/ie5007596
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The potential of Initiators for Continuous Activator Regeneration Atom Transfer Radical Polymerization (ICAR ATRP) to determine reliable Arrhenius parameters for ATRP activation/deactivation of macrospecies is illustrated using styrene as monomer and CuBr2/TPMA (TPMA: tris(2-pyridylmethyl)amine) as deactivator. Regression is based on an extensive set of experimental data limited to conversions below 0.50 to avoid the interference of diffusional limitations on the activation/deactivation process and recorded at temperatures below 90 degrees C to avoid the influence of thermal self-initiation. Diffusional limitations on termination are accounted for based on literature data. The activation energy for the activation and deactivation reaction involving macrospecies are respectively 29 and 1.7 kJ mol(-1). The corresponding pre-exponentional factors are 6.9 x 10(5) and 1.8 x 10(7) L mol(-1) s(-1). At 70 degrees C, the corresponding rate coefficients amount to 2.2 x 10 and 9.9 x 10(6) L mol(-1) s(-1) confirming the relatively high activity of CuBr/TPMA as ATRP catalyst.
引用
收藏
页码:9674 / 9685
页数:12
相关论文
共 59 条
  • [1] A review of modeling of diffusion controlled polymerization reactions
    Achilias, Dimitris S.
    [J]. MACROMOLECULAR THEORY AND SIMULATIONS, 2007, 16 (04) : 319 - 347
  • [2] Chain Transfer to Polymer and Branching in Controlled Radical Polymerizations of n-Butyl Acrylate
    Ahmad, Nasir M.
    Charleux, Bernadette
    Farcet, Celine
    Ferguson, Christopher J.
    Gaynor, Scott G.
    Hawkett, Brian S.
    Heatley, Frank
    Klumperman, Bert
    Konkolewicz, Dominik
    Lovell, Peter A.
    Matyjaszewski, Krzystof
    Venkatesh, Rajan
    [J]. MACROMOLECULAR RAPID COMMUNICATIONS, 2009, 30 (23) : 2002 - 2021
  • [3] Barner-Kowollik C., 2012, ENCY RADICALS CHEM B
  • [4] Chain-length-dependent termination in radical polymerization: Subtle revolution in tackling a long-standing challenge
    Barner-Kowollik, Christopher
    Russell, Gregory T.
    [J]. PROGRESS IN POLYMER SCIENCE, 2009, 34 (11) : 1211 - 1259
  • [5] BarnerKowollik C., 2008, Handbook of RAFT Polymerization
  • [6] Kinetic modeling of miniemulsion nitroxide mediated polymerization of styrene: Effect of particle diameter and nitroxide partitioning up to high conversion
    Bentein, L.
    D'hooge, D. R.
    Reyniers, M. -F.
    Marin, G. B.
    [J]. POLYMER, 2012, 53 (03) : 681 - 693
  • [7] Kinetic Modeling as a Tool to Understand and Improve the Nitroxide Mediated Polymerization of Styrene
    Bentein, Lien
    D'hooge, Dagmar R.
    Reyniers, Marie-Francoise
    Marin, Guy B.
    [J]. MACROMOLECULAR THEORY AND SIMULATIONS, 2011, 20 (04) : 238 - 265
  • [8] Brandup J., 1999, POLYM HDB, V4th
  • [9] Controlled/living radical polymerization: Features, developments and perspectives (vol 32, pg 93, 2007)
    Braunecker, Wade A.
    Matyjaszewski, Krzysztof
    [J]. PROGRESS IN POLYMER SCIENCE, 2008, 33 (01) : 165 - 165
  • [10] CRITICALLY EVALUATED RATE COEFFICIENTS FOR FREE-RADICAL POLYMERIZATION .1. PROPAGATION RATE COEFFICIENT FOR STYRENE
    BUBACK, M
    GILBERT, RG
    HUTCHINSON, RA
    KLUMPERMAN, B
    KUCHTA, FD
    MANDERS, BG
    ODRISCOLL, KF
    RUSSELL, GT
    SCHWEER, J
    [J]. MACROMOLECULAR CHEMISTRY AND PHYSICS, 1995, 196 (10) : 3267 - 3280