Design of Experiment (DoE) as a Tool for the Optimization of Source Conditions in SEC-ESI-MS of Functional Synthetic Polymers Synthesized via ATRP

被引:48
作者
Gruendling, Till [1 ,2 ]
Guilhaus, Michael [2 ]
Barner-Kowollik, Christopher [1 ]
机构
[1] Univ Karlsruhe TH, Karlsruhe Inst Technol KIT, Inst Tech & Polymerchem, D-76128 Karlsruhe, Germany
[2] Univ New S Wales, UNSW Analyt Ctr, Bioanalyt Mass Spectrometry Facil, Sydney, NSW 2052, Australia
关键词
design of experiment (DoE); ESI source optimization; ionization efficiency; poly(methyl methacrylate); radical polymerization; response surface design; reversible addition fragmentation chain transfer (RAFT); size exclusion chromatography electrospray ionization mass spectrometry (SEC-ESI-MS); IONIZATION-MASS-SPECTROMETRY; MOLECULAR-WEIGHT DISTRIBUTIONS; END-GROUP ANALYSIS; ELECTROSPRAY-IONIZATION; RADICAL POLYMERIZATION; POLY(METHYL METHACRYLATE); LIQUID-CHROMATOGRAPHY; DOEHLERT DESIGN; MALDI; POLYSTYRENES;
D O I
10.1002/marc.200800738
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Design of experiment (DoE) is applied to establish the optimum ionization conditions for analyzing synthetic polymers via coupled size exclusion chromatography electrospray ionization mass spectrometry (SEC-ESI-MS) yielding maximum ionization efficiency. The ion source conditions were optimized with regard to the ionization efficiency, the amount of fragmentation, as well as the formation of salt adducts. A D-optimal experimental design was employed for this purpose and the recorded data were evaluated by a quadratic response surface model, accounting for possible interactions between the individual source settings. It was established that the ionization efficiency can be improved by up to one order of magnitude without compromising the softness of the ionization process and that optimal ionization conditions are found at similar source settings regardless of the charge state. The present optimization exercise therefore provides a hands-on guide for the use of experimental design to determine optimum ionization conditions during the SEC-ESI-MS of functional polymers.
引用
收藏
页码:589 / 597
页数:9
相关论文
共 41 条
[1]   Gel permeation chromatography coupled to Fourier transform mass spectrometry for polymer characterization [J].
Aaserud, DJ ;
Prokai, L ;
Simonsick, WJ .
ANALYTICAL CHEMISTRY, 1999, 71 (21) :4793-4799
[2]   On the signal response of various pesticides in electrospray and atmospheric pressure chemical ionization depending on the flow-rate of eluent applied in liquid chromatography-tandem mass spectrometry [J].
Asperger, A ;
Efer, R ;
Koal, T ;
Engewald, W .
JOURNAL OF CHROMATOGRAPHY A, 2001, 937 (1-2) :65-72
[3]   Complex macromolecular architectures by reversible addition fragmentation chain transfer chemistry: Theory and practice [J].
Barner, Leonie ;
Davis, Thomas P. ;
Stenzel, Martina H. ;
Barner-Kowollik, Christopher .
MACROMOLECULAR RAPID COMMUNICATIONS, 2007, 28 (05) :539-559
[4]   Probing mechanistic features of conventional, catalytic and living free radical polymerizations using soft ionization mass spectrometric techniques [J].
Barner-Kowollik, C ;
Davis, TP ;
Stenzel, MH .
POLYMER, 2004, 45 (23) :7791-7805
[5]  
Barner-Kowollik C., 2008, Handbook of RAFT Polymerization
[6]  
Bednarek M, 2000, MACROMOL CHEM PHYSIC, V201, P58, DOI 10.1002/(SICI)1521-3935(20000101)201:1<58::AID-MACP58>3.0.CO
[7]  
2-G
[8]   Evidence for the low thermal stability of poly(methyl methacrylate) polymer produced by atom transfer radical polymerisation [J].
Borman, CD ;
Jackson, AT ;
Bunn, A ;
Cutter, AL ;
Irvine, DJ .
POLYMER, 2000, 41 (15) :6015-6020
[9]   Electrospray ionization mass spectrometric end-group analysis of PMMA produced by radical polymerization using diacyl peroxide initiators [J].
Buback, Michael ;
Frauendorf, Holm ;
GUnzler, Fabian ;
Vana, Philipp .
POLYMER, 2007, 48 (19) :5590-5598
[10]   Initiation of radical polymerization by peroxyacetates:: Polymer end-group analysis by electrospray ionization mass spectrometry [J].
Buback, Michael ;
Frauendorf, Holm ;
Guenzler, Fabian ;
Vana, Philipp .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2007, 45 (12) :2453-2467