DIRECT TEMPERATURE RESOLVED HRMS OF FIRE-RETARDED POLYMERS BY IN-SOURCE PYMS ON AN EXTERNAL ION-SOURCE FOURIER-TRANSFORM ION-CYCLOTRON RESONANCE MASS-SPECTROMETER

Citation
Rma. Heeren et al., DIRECT TEMPERATURE RESOLVED HRMS OF FIRE-RETARDED POLYMERS BY IN-SOURCE PYMS ON AN EXTERNAL ION-SOURCE FOURIER-TRANSFORM ION-CYCLOTRON RESONANCE MASS-SPECTROMETER, Analytical chemistry, 67(21), 1995, pp. 3965-3970
Citations number
38
Categorie Soggetti
Chemistry Analytical
Journal title
ISSN journal
00032700
Volume
67
Issue
21
Year of publication
1995
Pages
3965 - 3970
Database
ISI
SICI code
0003-2700(1995)67:21<3965:DTRHOF>2.0.ZU;2-4
Abstract
Rapid microscale analysis with high mass accuracy is demonstrated by d irect temperature resolved desorption and pyrolysis from a Pt/Rh filam ent probe inside the external ion source of a 7-T FTICR-MS. High press ure generated during desorption and pyrolysis in the ion source does n ot interfere with analysis in the hydrocarbon-free UHV of the ICR cell , thus allowing short observation cycles at high resolution. The typic al conditions achieved, a mass resolution (m/Delta m)(50%) equals 50 0 00 at m/z 600 with cycle times of 100 ms, were used to analyze isobari c compound mixtures generated by pyrolysis of brominated fire-retarded polymers spiked with antimony-containing synergists. Unknown fire-ret arded polymer blends sampled from household appliances were found to c ontain brominated biphenyls, brominated diphenyl ethers, tetrabromoBis phenol-A and its butylated isomers, polystyrene, and antimony oxides. High-resolution temperature-resolved analysis by ''in-source'' pyrolys is FTICR-MS confirms the elemental composition. The resolution is suff icient to separate the nominally isobaric ions from the antimony(III) oxide (Sb4O6) synergist and the n-butyl ether derivative of tetrabromo Bisphenol-A.