Effects of experimental conditions on the molecular composition of maltenes and asphaltenes derived from oilsands bitumen: Characterized by negative-ion ESI FT-ICR MS

LiTao Wang¹, Chen He¹, YangLiu¹, SuoQi Zhao^1* , YaHe Zhang¹, ChunMing Xu¹, Keng H.Chung² and Quan Shi^1*

¹State Key Laboratory of Heavy Oil Processing, China University of Petroleum, Beijing 102249, China

²Well Resources Inc., 3919-149A Street, Edmonton, Alberta, T6R 1J8, Canada

^*Corresponding authors (email: sqzhao@cup.edu.cn; sq@cup.edu.cn)

DOI: 10.1007/s11426-013-4902-0

Keywords: asphaltene precipitation, experimental conditions, bulk properties, molecular composition, ESI FT-ICR MS

Abstract: A vacuum topped Canadian oilsands bitumen (VTB) was subjected to solvent precipitation and subsequently characterized by elemental analysis, gel permeation chromatograph (GPC), 1H-NMR spectroscopy and negative-ion electrospray ionization (ESI) Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS). Effects of experimental conditions such as solvent types (n-C₅, n-C₆, and n-C₇), solvent purity, and solvent washing time on asphaltenes yields, bulk composition, and molecular composition of detectable heteroatom compounds in ESI source were determined. Elemental nitrogen and sulfur were enriched in asphaltenes while elemental oxygen had comparable content in maltenes and asphaltenes. Molecular compo sition of asphaltenes varies with separation conditions. The N₁ and O₁ species identified by ESI FT-ICR MS were enriched in maltenes. The O₂ species exhibited two different double bond equivalents (DBE) distributions and solubility in normal paraffin solvents, indicating two types of molecular structures. Multi oxygen atom containing compounds mainly detected in asphal tenes. Compound class distributions are similar for maltenes derived from n-C₅, n-C₆, and n-C₇ , as well as for asphaltenes. The cyclic paraffin impurities in normal paraffin solvents had a significant influence on asphaltenes yields and heteroatom molecu lar composition. A portion of neutral N₁ species and acidic O₂ species adsorbed on asphaltenes could be dissolved by increas ing washing time. Cautions should be exercised when interpreting the properties and composition of asphaltenes obtained with different experimental conditions.