Underwater determination of calcium and strontium ions in oilfield produced water by laser-induced breakdown spectroscopy (LIBS)

Abstract

Laser-induced breakdown spectroscopy (LIBS) was applied to the determination of scaling ions in oilfield-produced water employing underwater measurements. Initially, the stability of plasma was verified using four different optical setups and expansion of the laser beam, and a combination of an achromatic lens with a meniscus lens were necessary to stabilize the plasma. Preliminary experiments demonstrated that only the determinations of Ca(II) and Sr(II) ions were feasible while the signal for the Mg(II) ion was absent and the sensitivity for Ba(II) was very low. The laser pulse repetition rate was evaluated and rates of 10 and 20 Hz provided a more stable breakdown in water compared to repetition rates of 2 to 7 Hz, besides imparting higher intense signals. The increase in salinity showed a small matrix effect, decreasing the sensitivities of the calibration curves by 8–13% when standard solutions with a salinity of 30‰ were used instead of water. Under optimized conditions with a laser pulse energy of 31 mJ, gate delay of 300 ns, gate width of 5.0 μs, repetition rate of 10 Hz, and accumulation of 500 laser shots, a linear range from 25 to 150 mg L⁻¹ was obtained, with limits of detection of 0.58 and 0.85 mg L⁻¹ for Ca(II) and Sr(II), respectively. The underwater determination of scaling ions in produced water by LIBS provided results that do not significantly differ from those obtained by inductively coupled plasma atomic emission spectroscopy (ICP OES) at a confidence level of 95%, with relative errors of up to 5.2%. These results demonstrate the potential of underwater LIBS measurements as an analytical tool for the determination of alkaline-earth metal ions in produced water, which can help the oil industry to overcome the problems related to scale formation.