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The characterization study of inhibited silica/silicate scale using vinyl sulfonated copolymer (VS-Co)

Autorzy
Sazali R.A.b. , Sorbie K. S. , Boak L. S. , Azman A. Z. , Mohd Saaid I.b. , Dollah A.b. , Kassim Shaari N.Z.b. , Ismail K.N.b.
Treść / Zawartość
Pełne teksty:
Sazali_jamme_2023_117_2.pdf
Identyfikatory
DOI
10.5604/01.3001.0053.6699
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Purpose Silica/silicate scale is a significant problem, especially in oilfield production during Alkaline Surfactant Polymer (ASP) flooding, where chemical inhibitors are the preferred method to prevent them. In this study, the effect of inhibitor vinyl sulfonated copolymer (VS-Co) on silica/silicate scale formation was analysed using X-Ray Diffraction (XRD) and Fourier-transform infrared spectroscopy (FTIR). Design/methodology/approach The functional group type of VS-Co are sulfonate ions, SO3-, and these interact in the scaling process. Bulk-inhibited scaling brine tests were conducted at 60°C and pH 8.5. During these tests, the silicon brine (with VS-Co) representing the inhibited ASP leachate was mixed with a magnesium brine representing the connate water to replicate reservoir conditions during ASP flooding. The samples tested in this study were non-inhibited Si/Mg mixed brine of 60 ppm Mg2+ and 940 ppm Si4+ (60Mg:940Si) as a blank, and inhibited 60Mg:940Si mixture with various VS-Co concentrations of 20 ppm, 50 ppm, and 100 ppm. The inhibition efficiency of the VS-Co was determined, followed by the characterisation study of the silica/silicate scale deposited from both test conditions. Findings The IR spectra of all 60Mg:940Si samples show a similar peak at 1050 cm-1 to 1080 cm-1, attributed to a Si-O covalent bond and a band at 790 cm-1 to 800 cm-1 showing the presence of Si-O-Si stretching. XRD patterns produced a broad scattering peak for all samples at 2θ of 24° showing that the samples are amorphous silica. For tests of high Mg2+ in the brine mix, 900Mg:940Si, a mix of crystalline silica and crystalline magnesium silicate was produced. Based on these results, it can be concluded that the scale formed even with 100 ppm of VS-Co present. Further studies are required to address how to mitigate scale formation effectively in the future. Research limitations/implications Based on the research conducted, we can conclude that the VS-Co alone could not significantly inhibit the formation of silica/silicate scale even at the highest concentration (100 ppm) of VS-Co. However, having VS-Co present caused an alteration in IR spectra frequency which requires further investigation to assess how best to develop the inhibiting properties of the VS-Co product. The application of nanoparticles and their successful stories spark the interest of authors in searching for an efficient method of managing the silica/silicate scale where the modification of potential scale inhibitor (SI) with nanoparticles may be able to improve the inhibition efficiency towards the silicate/silicate scale. Practical implications The presence of VS-Co in the scaling brine only slightly inhibits the Mg2+ ion (initially comes from connate water) from reacting. It is worth further investigation on how this VS-Co can make it happen. Hence, the functional groups responsible for this may be altered by adding other functional groups to provide a synergistic effect in preventing this silica/silicate scale; or by modifying the VS-Co with nanoparticles to improve their adsorption/desorption capacity. Originality/value The newly developed technique in analysing the inhibition mechanism of a chemical inhibitor using various spectroscopic analysis is promising where an alteration in the spectra may provide proof of the chemical’s inhibition efficiency.
Słowa kluczowe
EN
PL
Wydawca
International OCSCO World Press
Czasopismo
Journal of Achievements in Materials and Manufacturing Engineering
Rocznik
2023
Tom
Vol. 117, nr 2
Strony
57--70
Opis fizyczny
Bibliogr. 52 poz., rys., wykr.
Twórcy
autor
Sazali R.A.b.
rozana592@uitm.edu.my
  • School of Chemical Engineering, College of Engineering, Universiti Teknologi MARA, Shah Alam, 40450, Selangor, Malaysia
autor
Sorbie K. S.
  • Flow Assurance and Scale Team, Institute of GeoEnergy Engineering, Heriot-Watt University, UK EH14 4AS, Edinburgh, Scotland, United Kingdom
  • School of Energy, Geoscience, Infrastructure and Society (EGIS), Heriot-Watt University, UK EH14 4AS, Edinburgh, Scotland, United Kingdom
autor
Boak L. S.
  • Flow Assurance and Scale Team, Institute of GeoEnergy Engineering, Heriot-Watt University, UK EH14 4AS, Edinburgh, Scotland, United Kingdom
  • School of Energy, Geoscience, Infrastructure and Society (EGIS), Heriot-Watt University, UK EH14 4AS, Edinburgh, Scotland, United Kingdom
autor
Azman A. Z.
  • School of Chemical Engineering, College of Engineering, Universiti Teknologi MARA, Shah Alam, 40450, Selangor, Malaysia
autor
Mohd Saaid I.b.
  • Centre of Research in Enhanced Oil Recovery (COREOR), Universiti Teknologi PETRONAS, 32610 Seri Iskandar, Perak, Malaysia
  • Petroleum Engineering Department, Faculty of Engineering, Universiti Teknologi PETRONAS, 32610 Seri Iskandar, Perak, Malaysia
autor
Dollah A.b.
  • School of Chemical Engineering, College of Engineering, Universiti Teknologi MARA, Shah Alam, 40450, Selangor, Malaysia
autor
Kassim Shaari N.Z.b.
  • School of Chemical Engineering, College of Engineering, Universiti Teknologi MARA, Shah Alam, 40450, Selangor, Malaysia
autor
Ismail K.N.b.
  • School of Chemical Engineering, College of Engineering, Universiti Teknologi MARA, Shah Alam, 40450, Selangor, Malaysia
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Uwagi
Opracowanie rekordu ze środków MNiSW, umowa nr SONP/SP/546092/2022 w ramach programu "Społeczna odpowiedzialność nauki" - moduł: Popularyzacja nauki i promocja sportu (2024).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-1bd96894-c19c-41a7-996b-ab4704fc37ae
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