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-groups. 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.
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Gies et al. (2009) studied this question.
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