Heavy and extra-heavy oils generally exhibit high viscosity, which is detrimental to their production, transport, and refining. The oil and gas industry has thoroughly investigated the use of chemical agents to improve the mobility of this type of low-quality crude oil at the surface as well as reservoir conditions for many years. In this sense, the main objective of this paper is to provide unexpected experimental evidence of heavy oil and extra-heavy crude oils viscosity reduction resulting from the presence of nanoparticles (NPs) of different chemical natures (SiO 2 , Fe 3 O 4 , and Al 2 O 3 ), particle size, surface acidity, and concentration at low-volume fractions. The viscosity of the enhanced fluids was measured using a rotational rheometer at shear rates varying between 1 and 75 s −1 . Upon addition of nanoparticles, viscosity reduction was observed in all cases evaluated. However, the maximum viscosity reduction of roughly 52% was obtained at a concentration of 1000 mg/L with 7 nm SiO 2 nanoparticles at shear rates below 10 s −1 , contrary to expectations from Einstein's viscosity theory in particulate systems. A mathematical model based on a modification to Pal and Rhodes Model for the viscosity of suspensions is proposed in this work. The said model that relates the concentration of nanoparticles to the fluid mixture viscosity was validated successfully using experimental data, as evidenced by RSME% values lower than 10%. The importance of our findings lies in the lack of previous experimental and theoretical data in the open literature showing heavy crude oil viscosity reduction in the presence of nanoparticles.
The main objective of this study is to evaluate the effect of the textural properties and surface chemical nature of silica nanoparticles obtained from different synthesis routes and silicon precursors, on their interactions with asphaltenes and further viscosity reduction of heavy crude oil (HO). Four different SiO 2 nanoparticles were used, namely, commercial fumed silica nanoparticles (CSNs) and three in-house-synthesized nanoparticles (named based on the silicon source) modifying the silicon precursor: sodium silicate (SNSS), tetraethylorthosilicate (TEOS) (SNT), and rice husk (SNRH). The nanomaterials were characterized through dynamic light scattering (DLS), transmission electron microscopy (TEM), Fourier transform infrared (FTIR) spectroscopy, N 2 physisorption (S BET ), atomic force microscopy (AFM), and X-ray photoelectron (XP) spectroscopy (XPS). The adsorption of asphaltenes over the different nanoparticles was evaluated at a concentration of 1000 mg•L −1 in toluene. The asphaltene−nanoparticle interactions are closely related to several textural properties, such as roughness, surface area, and hydrodynamic diameter, as well as the surface chemical nature of the materials. The results in the textural characterization exhibited that the sizes of the nanoparticles from TEM ranged between 6.9 and 11.5 nm. Nevertheless, the standard deviation of the measurements showed that the sizes are statistically similar. Inversely, the hydrodynamic diameter changed, affecting the surface silanol group's availability due to a hindering effect on functional groups as the hydrodynamic size of the material increased. The rheological measurements were performed at a fixed nanoparticle dosage of 1000 mg•L −1 and showed that the trend of the degree of viscosity reduction (DVR) was CSN > SNT > SNSS > SNRH with the highest value yielding at 30%. The results of DVR are in accordance with the nanoparticles' adsorptive capacity as higher values were obtained with the material that leads to a higher amount of adsorbed asphaltenes. Also, the oxygen amount related to silanol groups, estimated by the XPS analysis, showed a direct relation regarding adsorption capacity and further HO viscosity reduction.
The primary objective of this study is the development of nanofluids based on different diluent/dispersant ratios (DDR) for extra-heavy oil (EHO) viscosity reduction and its perdurability over time. Different diluents such as xylene, diesel, n-pentane, and n-heptane were evaluated for the formulation of the carrier fluid. Instability of asphaltenes was assessed for all diluents through colloidal instability index (CII) and Oliensis tests. Rheology measurements and hysteresis loop tests were performed using a rotational rheometer at 30 °C. The CII values for the alkanes type diluents were around 0.57, results that were corroborated with the Oliensis tests as asphaltenes precipitation was observed with the use of these diluents. This data was related to the viscosity reduction degree (VRD) reported for the different diluents. With the use of the alkanes, the VRD does not surpass the 60%, while with the use of xylene a VRD of approximately 85% was achieved. Dimethylformamide was used as a dispersant of the nanoparticles and had a similar VRD than that for xylene (87%). Subsequent experiments were performed varying the DDR (xylene/dimethylformamide) for different dosages up to 7 vol % determining that a DDR = 0.2 and a dosage of 5 vol % was appropriated for enhancing EHO VRD, obtaining a final value of 89%. Different SiO2 nanoparticles were evaluated in the viscosity reduction tests reporting the best results using 9 nm nanoparticles that were then included at 1000 mg·L−1 in the carrier fluid, increasing the VRD up to 4% and enhancing the perdurability based on the rheological hysteresis and the viscosity measurements for 30 days. Results showed a viscosity increase of 20 and 80% for the crude oil with the nanofluid and the carrier fluid after 30 days, respectively. The nanoparticles have a synergistic effect in the viscosity reduction and the inhibition of the viscoelastic network re-organization (perdurability) after treatment application which was also observed in the rheological modeling carried out with Cross and Carreau models as the reported characteristic relaxation time was increased almost a 20%. Moreover, the Vipulanandan rheological model denotes a higher maximum stress value reached by the EHO with the addition of nanofluids which is derived from the EHO internal structure rearrangement caused by the asphaltenes adsorption phenomenon.
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