Calcium carbonate scaling causes significant damage and financial losses to various industries, particularly in deep-water oil exploration. It is affected by factors like pressure, temperature, pH, solution chemistry, and surface finish. Surface finish is critical, as it interacts with the fluid and serves as a substrate for the anchoring of calcium carbonate crystals. However, many studies investigate this phenomenon under conditions that differ from those encountered in deep-water oil exploration. Tests are commonly performed under atmospheric pressure and lacking fluid flow or CO2 influence, which limits their relevance to industrial conditions. This study aims to evaluate the influence of surface finish on the formation of calcium carbonate scaling under conditions that more closely resemble actual operating environments. 304 stainless steel was selected to replicate industrial conditions, owing to its chemical stability and common use in industrial settings. The tests were conducted in a plant with high-pressure capabilities, operating under continuous flow conditions with CO2 injection. Controlled surfaces were prepared through metallographic polishing, machining, sandblasting, and laser texturing techniques. Surface characterization was performed using a 3D optical profilometer and scratch testing to measure the average adhesion force. The polymorphs formed were characterized by Raman spectroscopy. Fractal dimension analysis was applied to quantify the complexity of the analyzed surfaces. The results indicate that surfaces with higher fractal dimensions exhibit greater scaling mass and higher adhesion force. The main polymorph observed was calcite. Additionally, it was noted that the texture orientation relative to the flow affects scaling, with higher scaling values observed on surfaces oriented perpendicular to the flow. These findings are crucial for optimizing material selection and surface treatments in deep-water oil exploration, enhancing operational efficiency and reducing costs.
Inorganic scale formation in oil wells is a major flow assurance challenge, causing production losses, increased intervention costs and reduced operational efficiency. In Brazil, recent discoveries in pre-salt reservoirs have increased the relevance of calcium carbonate (CaCO3) scaling under high-pressure and high-temperature (HPHT) conditions. Experimental data representative of petroleum environments under such conditions, particularly regarding the influence of CO2 and flow conditions, remain limited. In this study, a compact pressurized experimental unit was designed and constructed to investigate the dynamic formation, deposition and adhesion of CaCO3 under conditions close to those encountered in oil production systems. A dedicated experimental methodology was developed to promote controlled mixing of aqueous sodium bicarbonate (NaHCO3) and calcium chloride (CaCl2) solutions and CO2 injection, enabling precise control of pressure, temperature and flow regime. The effects of turbulent flow, expressed by different Reynolds numbers, on the deposited CaCO3 mass and its adhesion to the substrate were systematically evaluated under controlled conditions of 40 °C and a pressure drop of 15 bar was imposed in the control valve in order to promote the flash of CO2 and CaCO3 precipitation. Complementary characterization analyses were performed to assess crystal morphology and adhesion detachment strength. The results provide new experimental insights into CaCO3 scaling mechanisms under CO2-rich flowing conditions, contributing to improved understanding of scale adhesion and the development of mitigation strategies for flow assurance in oil and gas operations.