MALDI-TOF/TOF CID Study of Poly(p-phenylene sulfide) Fragmentation Reactions

被引:13
作者
Gies, Anthony P. [1 ]
Geibel, Jon F. [2 ]
Hercules, David M. [1 ]
机构
[1] Vanderbilt Univ, Dept Chem, Nashville, TN 37235 USA
[2] Chevron Phillips Chem Co LP, Bartlesville Technol Ctr, Bartlesville, OK 74004 USA
关键词
MASS-SPECTRAL ANALYSIS; TEMPERATURE PYROLYSIS PRODUCTS; STEPWISE PY-GC/MS; THERMAL-DEGRADATION; POLY(PHENYLENE SULFIDE); POLY(ARYLENE SULFONE)S; SPECTROMETRY; MECHANISM; GROWTH;
D O I
10.1021/ma902118s
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A study involving the evaporation-grinding MALDI sample preparation method, MALDI-TOF/TOF CID, and Py-GC/MS is presented to examine the fragmentation mechanisms of poly(p-phenylene sulfide) (PPS). MALDI-TOF/TOF CID fragmentation studies yielded a wealth of information about the mass, structure (linear or cyclic), end-groups, and backbone modifications of the polymer. Additionally, Py-GC/MS experimental data are presented for comparison of the multimolecular free radical reactions in pyrolysis with the unimolecular fragmentation reactions of MS/MS.(1,2) TOF/TOF CID results indicate that linear PPS undergoes random main chain Fragmentation along the polymer backbone and preferentially fragments at bonds adjacent to dibenzothiophene and phenyl end-ggroups. Cyclic species produce fragment ions similar to linear species. However, the MS/MS precursor ions for cyclic PPS are, by far, the most intense peaks, while the precursor ions for linear species show relatively low intensity. CID fragmentation results are supported by Py-GC/MS data and are consistent with the proposed degradation mechanisms.
引用
收藏
页码:952 / 967
页数:16
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