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Surfactant loss control in chemical flooding spectroscopic and calorimetric study of adsorption and precipitation on reservoir minerals. Annual report, September 30, 1993--September 30, 1994
Author(s) -
P. Somasundaran
Publication year - 1995
Publication title -
osti oai (u.s. department of energy office of scientific and technical information)
Language(s) - English
Resource type - Reports
DOI - 10.2172/80984
Subject(s) - pulmonary surfactant , adsorption , chemistry , chemical engineering , sodium dodecyl sulfate , desorption , inorganic chemistry , critical micelle concentration , surface charge , chromatography , micelle , organic chemistry , aqueous solution , biochemistry , engineering
The aim of this project is to elucidate the mechanisms underlying adsorption and surface precipitation of flooding surfactants on reservoir minerals. Effect of surfactant structure, surfactant combinations, other inorganic and polymeric species is being studied. A multi-pronged approach consisting of micro and nano spectroscopy, microcalorimetry, electrokinetics, surface tension and wettability is used to achieve the goals. The results of this study should help in controlling surfactant loss in chemical flooding and also in developing optimum structures and conditions for efficient chemical flooding processes. During the second year of this three year contract, adsorption/desorption of single surfactants and select surfactant mixtures on alumina and silica was studied. Surfactants studied include the anionic sodium dodecyl sulfate (SDS), cationic tetradecyl trimethyl ammonium chloride (TTAC), nonionic pentadecylethoxylated nonyl phenol (NP-15) and the nonionic octaethylene glycol n-dodecyl ether (C{sub 12}EO{sub 8}) of varying hydrocarbon chain length. The microstructure of the adsorbed layer in terms of micropolarity and aggregation numbers was probed using fluorescence spectroscopy. Changes of microstructure upon dilution (desorption) were also studied. Presence of the nonionic surfactant in the mixed aggregate led to shielding of the charge of the ionic surfactant which in-turn promoted aggregation but reduced electrostatic attraction between the charged surfactant and the mineral surface. Strong consequences of surfactant interactions in solution upon adsorption as well as correlations between monomer concentrations in mixtures and adsorption were revealed

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