Critically evaluated termination rate coefficients for free-radical polymerization: Experimental methods

被引:114
|
作者
Barner-Kowollik, C
Buback, M
Egorov, M
Fukuda, T
Goto, A
Olaj, OF
Russell, GT [1 ]
Vana, P
Yamada, B
Zetterlund, PB
机构
[1] Univ New S Wales, Sch Chem Engn & Ind Chem, Ctr Adv Macromol Design, Sydney, NSW 2052, Australia
[2] Univ Gottingen, Inst Phys Chem, D-37077 Gottingen, Germany
[3] Kyoto Univ, Inst Chem Res, Uji, Kyoto 6110011, Japan
[4] Univ Vienna, Inst Phys Chem, A-1090 Vienna, Austria
[5] Univ Canterbury, Dept Chem, Christchurch, New Zealand
[6] Osaka City Univ, Fac Engn, Dept Appl Chem, Osaka 5528585, Japan
[7] Kobe Univ, Grad Sch Sci & Technol, Nada Ku, Kobe, Hyogo 6578501, Japan
关键词
free-radical polymerization; kinetics; termination rate coefficients; pulsed-laser polymerization; molecular weight distributions;
D O I
10.1016/j.progpolymsci.2005.02.001
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 knowledge of accurate rate coefficients for individual steps of free-radical polymerization (FRP) is of scientific interest and of application-oriented importance. For a wide variety of homopolymerizations and for many copolymerizations, reliable propagation rate coefficients, k(P), are accessible via the IUPAC-reconiniended method of PLP-SEC (pulsed laser polymerization-size-exclusion chromatography). For termination rate coefficients, k(t). the situation is less favorable. Even for very common monomers, no k(t) benchmark data sets are available. Moreover, instead of having one recommended technique for measuring k(t). there are a plethora of such methods. Seventeen of the most prominent approaches for measuring k(t) are here reviewed, including innovative ones that have emerged over the last decade. The methods have been subdivided into two categories: (i) 'Kinetic methods', in which analysis of the time dependence of concentrations is essential, and (ii) 'MWD methods', in which the analysis of the molecular weight distribution plays the dominant role. The methods are evaluated with respect to their potential for providing routine access to measuring k(t) as a function of monomer conversion and of free-radical chain length. Moreover, it has been considered whether expensive instrumentation or highly demanding analysis is required for a particular method and whether a method is applicable to many types of monomers. A table summarizes all these evaluations in a readily accessible form. The use of kinetic methods appears to be generally preferable over MWD-based methods. The largest potential is currently seen for methods in which polymerization is induced by a single laser pulse and where the subsequent time evolution of either monomer concentration or free-radical concentration is measured. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:605 / 643
页数:39
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