Summary
Surfactant-based acid systems were developed over the last few years for
diversion to overcome the severe problems caused by polymer residue and
crosslinker precipitate after polymer-based system treatments during matrix and
fracture acidizing. Two main types of viscoelastic surfactants have been used:
amphoteric and cationic. Surfactant molecules can form rod-like micelles and
significantly increase the viscosity in the presence of salts. After acid
treatments, the surfactant gel can be broken by mixing with hydrocarbons,
external breakers, internal breakers, or by reducing the concentration of salts
and or surfactant through dilution with water.
This paper introduces a new type of viscoelastic-amphoteric surfactant
(amine oxide). It carries a positive charge in live HCl acids. The effects of
acid additives and Fe(III) contamination were examined on its rheological
properties. Measurements were made at temperatures from 75 to 220°F and 300 psi
at various shear rates from 0.01 to 935 sec–1. Acid additives
included corrosion inhibitors, a mutual solvent, a nonemulsifying surfactant,
iron-control agents, and a hydrogen-sulfide scavenger.
The apparent viscosity of surfactant solutions prepared in deionized water,
live acid, and spent acid was found to be a function of temperature. Apparent
viscosity of live surfactant-based acids was also found to be a function of HCl
concentration. Fe(III) contamination caused enhancement of apparent viscosity,
then two immiscible liquids, and finally precipitation of surfactant/Fe
complex. A demulsifer and mutual solvent decreased the apparent viscosity at
all temperatures examined. Multiple iron-control agents were tested and found
to reduce the apparent viscosity of this surfactant-based acid. Only up to 1
wt% methanol can be used with this spent-acid system at temperatures below
175°F.
© 2010. Society of Petroleum Engineers
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History
- Original manuscript received:
26 February 2009
- Meeting paper published:
20 April 2009
- Revised manuscript received:
10 September 2009
- Manuscript approved:
25 November 2009
- Published online:
11 March 2010
- Version of record:
11 August 2010