SPE Production & Operations
Volume 24, Number 2, May 2009, pp. 360-368

SPE-125203-PA

Verification of Asphaltene-Instability-Trend (ASIST) Predictions for Low-Molecular-Weight Alkanes

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DOI  More information 10.2118/125203-PA http://dx.doi.org/10.2118/125203-PA

Citation

  • Creek, J.L., Wang, J., and Buckley, J.S. 2009. Verification of Asphaltene-Instability-Trend (ASIST) Predictions for Low-Molecular-Weight Alkanes. SPE Prod & Oper  24 (2): 360-368. SPE-125203-PA.

Discipline Categories

  • 4.6.3 Asphaltenes
  • 5.5.1 Asphaltenes, Hydrates, Precipitates, Scale, Waxes (Inhibition and Remediation)
  • 4.6.2 Paraffin
  • 5.1.3 Downhole Intervention
  • 5.2.6 Gas Lift

Keywords

  • asphaltene, onset prediction, ASIST, solubility

Summary

Anticipating when and where asphaltenes may flocculate during oil production is a key step in successfully preventing or mitigating asphaltene problems in the field. Because there will be no deposition without precipitation, mapping of asphaltene stability over a wide range of temperature, pressure, and composition is required. The asphaltene-instability-trend (ASIST) allows the determination of the onset of asphaltene instability to be established with a series of liquid n-alkanes. These data are used to predict asphaltene stability of live fluids by extrapolating the onset condition from the base data to reservoir conditions by use of a linear extrapolation of the onset solubility parameter vs. square root of the partial molar volume of the precipitant. This extrapolation has been demonstrated previously to be accurate for methane and a model oil. The present work verifies that such an extrapolation is valid for predicting the asphaltene instability for mixtures of methane, ethane, and propane with a representative stock-tank oil (STO). The STO was combined with known amounts of methane, ethane, or propane. The asphaltene onset pressure was determined by a combination of near-infrared (NIR) light scattering and microscopic observation. The onset conditions at ambient pressures were examined for flocculation periods ranging from 20 minutes to 24 hours. Onset pressures calculated with the 5-hour ASIST trends compared well with measured onset pressures.

Introduction

Asphaltenes are materials in a crude oil that are among the highest molecular weight and/or those with the highest degree of polarity (Long 1981) and aromaticity (Cimino et al. 1995). These large molecules have limited solubility in saturated hydrocarbons, tend to form aggregates that are dispersed in crude oils, and form separate heavy phases in response to changes in pressure, temperature, or composition of the oil mixture. The amount of material that separates (asphaltene amount) and the solubility conditions at which separation occurs (asphaltene-flocculation onset) vary not only with the composition of the asphaltenes themselves, but also with the size of the paraffinic precipitants, whether these are the native crude-oil light ends or added nonsolvents (typically, n-pentane or n-heptane).

Wang (2000) demonstrated that asphaltene onset conditions--defined in terms of the mixture refractive index (RI), which for nonpolar species can be related to the mixture solubility parameter (δ) (Buckley et al. 1998)--changed predictably with molar volume of n-alkane precipitating agents. Extrapolation of the relationship established by measurements with liquid n-alkanes to predict asphaltene instability during depressurization was proposed (Wang and Buckley 2001a). Numerous successful applications of ASIST (Buckley et al. 2007) have since been published (e.g., Wang et al. 2004) suggesting that extrapolation of the ASIST relationship is reasonable. Nevertheless, direct verification is needed of the link between asphaltene instability, upon addition of normal alkanes, and the asphaltenes that appear during depressurization of a crude oil.

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History

  • Original manuscript received: 4 February 2008
  • Meeting paper published: 5 May 2008
  • Revised manuscript received: 16 September 2008
  • Manuscript approved: 3 October 2008
  • Published online: 1 May 2009
  • Version of record: 1 May 2009