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