Molecular characterization of petroporphyrins in crude oil by electrospray ionization Fourier transform ion cyclotron resonance mass spectrometry

被引:95
作者
Rodgers, RP
Hendrickson, CL
Emmett, MR
Marshall, AG
Greaney, M
Qian, KN
机构
[1] Florida State Univ, Ctr Interdisciplinary Magnet Resonance, Natl High Magnet Field Lab, Tallahassee, FL 32310 USA
[2] ExxonMobil Res & Engn, Annandale, NJ 08801 USA
关键词
petroporphyrin; porphyrin; petroleum; electrospray ionization; mass spectrometry; Fourier transform; ion cyclotron resonance; ICR; FT-ICR; FTMS;
D O I
10.1139/cjc-79-5-6-546
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Petroporphyrin compositional analysis of a heavy crude oil has been realized by isolation and subsequent ESI-FT-ICR mass spectrometric analysis of the porphyrin-containing fractions. Vanadium octaethyl (V=O(II)OEP) and nickel octaethyl (Ni(II)OEP) porphyrin standards were analyzed to determine favorable electrospray ionization conditions and provide insight as to the molecular species present (e.g., adducts, multimers). Standard V=O(II)OEP and Ni(II)OEP solutions revealed the presence of both monomer and dimer species with a greater relative abundance of monomers. In contrast, mass spectral analysis of a porphyrin fraction from Cerro Negro crude oil was dominated by dimeric species. MS3 analysis identified a dioctylphthalate (DOP) contaminant, likely introduced during fractionation of the crude oil. DOP-porphyrin complexes and porphyrin-porphyrin dimers were then identified. Infrared multiphoton dissociation (IRMPD) of dimeric species produced the corresponding monomers with minimal fragmentation. The monomeric petroporphyrins were analyzed to reveal the metal (Ni(II) or V=O(II)), porphyrin type (e.g., etio vs. DPEP), and distribution of alkylation.
引用
收藏
页码:546 / 551
页数:6
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