Petroleomics by Direct Analysis in Real Time-Mass Spectrometry

被引:23
作者
Romao, Wanderson [1 ,2 ]
Tose, Lilian V. [1 ]
Vaz, Boniek G. [3 ]
Sama, Sara G. [4 ,5 ]
Lobinski, Ryszard [4 ]
Giusti, Pierre [5 ]
Carrier, Herve [6 ]
Bouyssiere, Brice [4 ]
机构
[1] Univ Fed Espirito Santo, Dept Quim, Lab Petr & Forense, Vitoria 29075910, ES, Spain
[2] Inst Fed Educ Cincia & Tecnol Espirito Santo, BR-29106010 Vila Velha, ES, Brazil
[3] Univ Fed Goias, Inst Quim, Goiania, Go, Brazil
[4] Univ Pau & Pays Adour, LCABIE IPREM, F-64053 Pau, France
[5] TOTAL Raffinage Chim, TRTG, Harfleur, France
[6] Univ Pau & Pays Adour, LFR R, F-64012 Pau, France
关键词
Ambient mass spectrometry; DART; Crude oil; Paraffin; Porphyrin; IONIZATION; HYDROCARBONS; OXIDATION; AIR;
D O I
10.1007/s13361-015-1266-z
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The analysis of crude oil and its fractions by applying ambient ionization techniques remains underexplored in mass spectrometry (MS). Direct analysis in real time (DART) in the positive-ion mode was coupled to a linear quadrupole ion trap Orbitrap mass spectrometer (LTQ Orbitrap) to analyze crude oil, paraffin samples, and porphyrin standard compounds. The ionization parameters of DART-MS were optimized for crude oil analysis. DART-MS rendered the optimum conditions of the operation using paper as the substrate, T = 400A degrees C, helium as the carrier gas, and a sample concentration a parts per thousand yen6 mg mL(-1). In the crude oils analysis, the DART(+)-Orbitrap mass spectra detected the typical N, NO, and O-containing compounds. In the paraffin samples, oxidized hydrocarbon species (O-x classes, where x = 1-4) with double-bond equivalent of 1-4 were detected, and their structures and connectivity were confirmed by collision-induced dissociation (CID) experiments. DART(+)-MS has identified the porphyrin standard compounds as [M + H](+) ions of m/z 615.2502 and 680.1763, where M = C44H30N4 and C44H28N4OV, respectively, based on the formula assignment and by phenyl losses observed on CID experiments.
引用
收藏
页码:182 / 185
页数:4
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