首页 | 本学科首页   官方微博 | 高级检索  
     


Investigation of Asphaltene Precipitation Process for Kuwaiti Reservoir
Abstract:Abstract

As part of an Enhanced Oil Recovery (EOR) research program, Asphalting precipitation processes were investigated for a Kuwaiti dead oil sample using different hydrocarbons and carbon dioxide as precipitants at the ambient and high pressure of 3000 psig conditions. The hydrocarbons used as precipitants were ethane (C2), propane (C3), butane (C4), normal pentane (n-C5), normal hexane (n-C6), and normal heptane (n-C7). The equipment used for this investigation was a mercury-free, variable volume, fully visual JEFRI-DBR PVT system with laser light scattering. The minimum critical value of precipitants concentration for the oil sample has been identified at the ambient and high-pressure conditions for each precipitant. Our investigation has revealed that for this oil sample the most powerful asphaltene precipitant were CO2 followed by C2, C3, C4, n-C5, n-C6, and n-C7. Moreover, the effect of pressure and temperature on the asphaltene precipitation has been investigated experimentally for CO2, n-C5, n-C6, and n-C7. The precipitation and redissolution of asphaltene upon the addition and removal of CO2 and light alkanes (C2–C4), at 3000 psig and ambient temperatures, have shown evidence of reversibility of asphaltene precipitation. A comprehensive fluid characterization analysis for the oil sample has been performed including, physical properties of crude oil, compositional, molecular weight (Mw), and SARA analyses. Advanced analytical techniques such as 1H and 13C NMR and IR spectrometers have been utilized to investigate the molecular structure of the asphaltene for this sample. It was concluded that the asphaltene molecules for this oil contain 120 total aromatic carbons with 42 aromatic rings, 114 naphthenic rings, and 5–7 sets of condensed aromatic rings.
Keywords:Asphaltene  Asphaltene precipitation  Alkanes precipitants  Asphaltene reversibility  Asphaltene in Kuwait  Asphaltene lab analysis
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号