SPE Journal
Volume 17, Number 4, December 2012, pp. 1172-1185

SPE-129907-PA

CO2-Soluble, Nonionic, Water-Soluble Surfactants That Stabilize CO2-in-Brine Foams

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DOI  More information 10.2118/129907-PA http://dx.doi.org/10.2118/129907-PA

Citation

  • Xing, D., Wei, B., McLendon, W. et al. 2012. CO2-Soluble, Nonionic, Water-Soluble Surfactants That Stabilize CO2-in-Brine Foams. SPE J.  17 (4): 1172-1185. SPE-129907-PA. http://dx.doi.org/10.2118/129907-PA.

Summary

Several commercially available, nonionic surfactants were identified that are capable of dissolving in carbon dioxide (CO2) in dilute concentration at typical minimum- miscibility-pressure (MMP) conditions and, upon mixing with brine in a high-pressure windowed cell, stabilizing CO2-in-brine foams. These slightly CO2-soluble, water-soluble surfactants include branched alkylphenol ethoxylates, branched alkyl ethoxylates, a fatty-acid-based surfactant, and a predominantly linear ethoxylated alcohol. Many of the surfactants were between 0.02 to 0.06 wt% soluble in CO2 at 1,500 psia and 25°C, and most demonstrated some capacity to stabilize foam. The most- stable foams observed in a high-pressure windowed cell were attained with branched alkylphenol ethoxylates, several of which were studied in high-pressure small-angle-neutron-scattering (HP SANS) tests, transient mobility tests using Berea sandstone cores, and high-pressure computed-tomography (CT)-imaging tests using polystyrene cores. HP SANS analysis of foams residing in a small windowed cell demonstrated that the nonylphenol ethoxylate SURFONIC® N-150 [15 ethylene oxide (EO) groups] generated emulsions with a greater concentration of droplets and a broader distribution of droplet sizes than the shorter-chain analogs with 9-12 ethoxylates. The in-situ formation of weak foams was verified during transient mobility tests by measuring the pressure drop across a Berea sandstone core as a CO2/surfactant solution was injected into a Berea sandstone core initially saturated with brine; the pressure-drop values when surfactant was dissolved in the CO2 were at least twice those attained when pure CO2 was injected into the same brine-saturated core. The greatest mobility reduction was achieved when surfactant was added both to the brine initially in the core and to the injected CO2. CT imaging of CO2 invading a polystyrene core initially saturated with 5 wt% KI brine indicated that despite the oil-wet nature of this medium, a sharp foam front propagated through the core, and CO2 fingers that formed in the absence of a surfactant were completely suppressed by foams formed because of the addition of nonylphenol ethoxylate surfactant to the CO2 or the brine.

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History

  • Original manuscript received: 20 April 2011
  • Meeting paper published: 24 April 2010
  • Revised manuscript received: 21 May 2012
  • Manuscript approved: 23 May 2012
  • Published online: 27 November 2012
  • Version of record: 7 December 2012