Abstract

Abstract Chelating agents are used to stimulate high-temperature carbonate reservoirs and remove mineral scales. For field applications, commercial chelates—EDTA, DTPA, GLDA, etc.—are commonly supplied as 35–50 wt% (1.2–1.7 M) solutions and diluted two times in water. However, the dependence of the reaction rate on the concentration of chelate in solution has never been quantified. This paper focuses on determining the kinetics of calcite dissolution as a function of the dilution factor of commonly used chelates at acidic pH. Using a rotating disk apparatus, the kinetics of calcite marble dissolution in 0.1–0.25 M EDTA (pH=4.9–5.0), 0.1–0.25 M DTPA (pH=3.5–5.0), and 0.28–0.85 M GLDA (pH=3.7–5.0) solutions has been investigated. The dissolution of calcite in all chelates has a negative fractional-order that increases with temperature in the range -0.6 < n < -1.9. Thus, less concentrated chelate solutions react faster with calcite, and the effect of chelate dilution becomes less pronounced with a temperature increase. For example, three times dilution of pH≈3.7 commercial GLDA solution—from commonly used 50 vol% (0.85 M) to 16.7 vol% (0.28 M)—increases calcite dissolution rate 8.4, 4.9, 2.7, and 2.0 times at 98.6, 116.6, 134.6, and 188.6°F, respectively. Dilution of pH=5.0 EDTA and pH=3.5 DTPA from 0.25 M to 0.1 M increases the dissolution rate of calcite 1.4–3.1 times at 98.6–188.6°F. Probable reasons for such an unusual reaction behavior are discussed in the paper. Presented results are integral for designing the stimulation operations in carbonate reservoir rocks and the removal of carbonate scales.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.