A Perfect Couple: PLP/SEC/ESI-MS for the Accurate Determination of Propagation Rate Coefficients in Free Radical Polymerization

被引:16
作者
Gruendling, Till [1 ,2 ]
Voll, Dominik [1 ]
Guilhaus, Michael [2 ]
Barner-Kowollik, Christopher [1 ]
机构
[1] KIT, Inst Tech Chem & Polymerchem, D-76128 Karlsruhe, Germany
[2] Univ New S Wales, UNSW Analyt Ctr, Bioanalyt Mass Spectrometry Facil, Sydney, NSW 2052, Australia
关键词
accurate propagation rate coefficients (k(p)); arrhenius equation; electrospray Ionization mass spectrometry (ESI-MS); pulsed laser polymerization (PLP); size exclusion chromatography (SEC); SIZE-EXCLUSION CHROMATOGRAPHY; PULSED-LASER POLYMERIZATION; FLIGHT MASS-SPECTROMETRY; MOLECULAR-WEIGHT DISTRIBUTIONS; EVALUATED RATE COEFFICIENTS; GEL-PERMEATION CHROMATOGRAPHY; CHAIN-LENGTH DEPENDENCE; ALKYL METHACRYLATES; SYNTHETIC-POLYMERS; POLYDISPERSE POLYMERS;
D O I
10.1002/macp.200900394
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Pulsed laser polymerization (PLP) in conjunction with online size exclusion chromatography electrospray ionization mass spectrometry (SEC/ESI-MS) has successfully been applied for the determination of accurate propagation rate coefficients, k(p), in free radical polymerization. SEC/ESI-MS is used in this context to precisely determine the molecular weight distribution of the polymer produced by the PLP-experiment. The novel approach allows for a highly accurate internal calibration of the size exclusion system to be obtained from first principles, as the molecular weight of the polymer is determined with ppm accuracy by the mass spectrometer and allows corrections for SEC band broadening effects to be made. Molecular weight measurements can furthermore be performed regardless of the monomer class, as long as the macromolecule is amenable to electrospray ionization. The proposed approach successfully eliminates work-steps and problems incurred in the analysis of new and poorly characterized monomers, where universal calibration or multi-detector SEC had to be applied until now and provides an alternative also to PLP/MALDI-MS. Applicability of the method is demonstrated for the homologous series of methyl-, ethyl- and butyl methacrylate. The experimentally determined k(p) values were 5-10% higher than the currently available benchmark data. The experimental k(p) is in agreement with the results of kinetic simulations, assuming a short chain length dependency of k(p), in accordance with the empirical model of Smith, Heuts and Russell.
引用
收藏
页码:80 / 90
页数:11
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