A method was developed to analyze direct trace and ultra-trace metal elements in crude oil and its fractions (maltenes-asphaltenes) by ICP-MS after sample dilution in xylene. Efficient introduction of organic compounds requires addition of O2 for complete combustion of the sample, carbon deposit on cones (interface) and extraction lenses was minimized by optimization of argon to oxygen ratio in the plasma. A PFA-100 (100 μl.mn−1) MicroFlow Nebulizer and a Scott “double pass” chilled spray chamber were associated for an optimal introduction of petroleum products. The Q-ICP/MS was equipped with platinum cones to limit drifts caused by cone corrosion during an organic analysis. A standard addition method was realized for the calibration procedure in order to control the matrix effects. Method validation was completed by analyzing three certified reference materials from the National Institute for Standards and Technology (NIST). NIST 1085b, NIST 1084a, and NIST 1634c accuracies were approximately 10 %. Detection limit of ultra trace elements in xylene were at pg.g−1 level. A clean PFA filter system was developed to separate the oil fractions (maltenes and asphaltenes) by precipitation of asphaltenes (heavy fraction) in n-heptane. For optimal detection conditions, the samples were diluted in xylene according to their pre-estimated element concentration range. Total mass balance shows a recovery close to 100 % for Ni, V, Cu, Mo, Ag, Sn, Ba, and Pb. These results show that elements analyzed are highly concentrated in the asphaltenic fraction.

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A method was developed to analyze direct trace and ultra-trace metal elements in crude oil nd its fractions (maltenes-asphaltenes) by ICP-MS after sample dilution in xylene. Efficient introduction of organic compounds requires addition of O2 for complete combustion of the sample; carbon deposit on cones (interface) and extraction lenses was minimized by optimization of argon to oxygen ratio in the plasma. A PFA-100 (100 μl.mn-1) MicroFlow Nebulizer and a Scott “double pass” chilled spray chamber were associated for an optimal introduction of petroleum products. The Q-ICP/MS was equipped with platinum cones to limit drifts caused by cone corrosion during an organic analysis. A standard addition method was realized for the calibration procedure in order to control the matrix effects. Method validation was completed by analyzing three certified reference materials from the National Institute for Standards and Technology (NIST). NIST 1085b, NIST 1084a, and NIST 1634c accuracies were approximately 10 %. Detection limit of ultra trace elements in xylene were at pg.g-1 level. A clean PFA filter system was developed to separate the oil fractions (maltenes and asphaltenes) by precipitation of asphaltenes (heavy fraction) in n-heptane. For optimal detection conditions, the samples were diluted in xylene according to their pre-estimated element concentration range. Total mass balance shows a recovery close to 100 % for Ni, V, Cu, Mo, Ag, Sn, Ba, and Pb. These results show that elements analyzed are highly concentrated in the asphaltenic fraction.