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The formation of mineral scale is an undesirable phenomenon which is as a result of the disturbances in thermodynamics and chemical equilibria of the water system. CaCO3 scale is one of the major flow challenges in the oil industry and the crystallization process starts from thermodynamically unstable hydrated form to anhydrous polymorphic stable forms1,2 The transformation involves a series of ordering, dehydration, and crystallization processes, each lowering the enthalpy of the system where the crystallization of the dehydrated amorphous material lowers the enthalpy the most. There are two theories regarding the polymorphic transformation of a solid structure. The first suggests the transformation occurs through a direct solid transition in which the metastable phase exhibits a rearrangement of its molecules or atoms to a more stable form3. The second is valid in the presence of a solvent which allows the dissolution and the re-nucleation and growth of the stable phase4.
Studying the kinetics of scale formation on the surface and in the bulk of the fluid when the oil phase is present has not yet received much attention. The impact of adding an oil phase to both surface deposition and bulk precipitation is not clear and needs to be studied. This work studies the mechanisms and behavior of precipitation of calcium carbonate scale in the presence of oil - water emulsion. A total of 100ml of different oil fractions including cyclohexane, kerosene, toluene and asphaltene is introduced to a vessel with 1000ml of brine at temperature, T=30°C. Using the Rotating Cylinder Electrode (RCE) technique, the mixture is continuously stirred with an overhead impeller blade at 520 rpm to create homogeneous dispersion in the two-phase mixture.
The incidence and proliferation of microbial population in oil and gas production facilities can have undesirable consequences on upstream, midstream and downstream production systems. Microbes thrive in the anaerobic conditions encountered in these systems and are supported by nutrients and metabolites found in produced water. Although the majority of process and water injection systems are susceptible to microbial fouling, the development of microbial activity is exacerbated by specific conditions such as stagnant fluids or the presence of deposits.1 Threats of microbiologically influenced corrosion (MIC) and other challenges associated with microorganisms have become valid as more cases are reported. While MIC, biofouling (BF), and reservoir souring are three of the most common problems associated with microbes, many other production issues can be attributable to microbial activity including: employee infections, filter plugging, loss of injectivity, and metal sulfide deposits.2
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Offshore wind farms are important contributions to the growing need for the generation of renewable energy. The number of offshore wind farms is growing, and multiple projects are under planning and construction around the world. One key element for a profitable and sustainable operation of offshore wind farms is that the installations are protected with the most cost-effective corrosion protective solution for the entire lifetime of the offshore wind farm. In practice, this means that today’s projects are planned with an estimated lifetime of a minimum of 35 years without major maintenance of the corrosion protective solution. To achieve this it is instrumental that the entire lifetime cost is considered when a corrosion protective solution is selected.
Many industrial processes contain H2, CO, CO2, and H2O gas mixtures, such as syngas production and processing in hydrogen, ammonia, and methanol plants. These process environments have high carbon activity, i.e. ac > 1, and low oxygen partial pressure at their elevated operating temperatures, such as in the temperature range of 400-800 °C (752-1472 °F). The high carbon activity could result in a catastrophic material degradation, i.e. metal dusting. The resulting corrosion products consist of carbon or graphite and metal particles, along with possible carbides and oxides, and cause material disintegration.