Simultaneous identification of different classes of hydrocarbons and determination of nitro-polycyclic aromatic hydrocarbons by means of particle beam liquid chromatography mass spectrometry

被引:45
作者
Bonfanti, L
Careri, M
Mangia, A
Manini, P
Maspero, M
机构
[1] UNIV PARMA, DIPARTIMENTO CHIM GEN & INORGAN CHIM ANALIT CHIM, I-43100 PARMA, ITALY
[2] CRT, ENEL, I-56100 PISA, ITALY
[3] CTR INFORMAZ STUDI & ESPERIENZE, I-20134 MILAN, ITALY
关键词
liquid chromatography mass spectrometry; particle beam interface; interfaces; LC-MS; hydrocarbons; polynuclear aromatic hydrocarbons;
D O I
10.1016/0021-9673(95)01040-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
LC-MS with a particle beam interface was used to separate and identify aliphatic hydrocarbons, polycyclic aromatic hydrocarbons (PAHs) and their nitrated derivatives (nitro-PAHs). In particular, the behaviour of nitro-PAHs and of two nitrated biphenyls was checked in terms of instrumental response. A normal-phase chromatographic system was used, with a silica column and heptane-tetrahydrofuran as mobile phase. Electron impact and positive- and negative-ion chemical ionization (NICI) modes were used; for nitro-PAHs, the best results were obtained under NICI conditions. In the flow-injection mode, detection limits as low as pg levels were obtained for 9-nitroanthracene, 3-nitro-9-fluorenone, 1-nitropyrene, 1,8-dinitronaphthalene, 2,7-dinitrofluorene and 2,7-dinitro-9-fluorenone, whereas the low-molecular-mass 1- and 2-nitronaphthalene were not detected even at mu g levels; using the analytical column, a detection limit five times higher was determined for 1-nitropyrene. For most of the nitro-PAHs considered, the dependences of the intensities on the amounts injected were found to be linear in a range of more than two orders of magnitude.
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页码:359 / 369
页数:11
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