TY - JOUR
T1 - A novel technique for heavy oil recovery using poly vinyl alcohol (PVA) and PVA-NaOH with ethanol additive
AU - Alade, Olalekan S.
AU - Al Shehri, Dhafer
AU - Mahmoud, Mohamed
AU - Mokheimer, Esmail M.A.
AU - Al Hamad, Jafar
AU - Kamal, Muhammad Shahzad
AU - Al-Nakhli, Ayman
AU - Sasaki, K.
N1 - Funding Information:
The authors of this article highly appreciate and acknowledge the support provided by the DSR of King Fahd University of Petroleum and Minerals (KFUPM) through the Internal Funded Project No. DF181017. Kyushu University are also highly appreciated for provision of research space and supports. The authors would like also to appreciate the Kuraray Company Japan for provision of the PVA samples.
Publisher Copyright:
© 2020 Elsevier Ltd
PY - 2021/2/1
Y1 - 2021/2/1
N2 - A novel enhanced oil recovery approach using PVA solution and PVA-NaOH mixtures (with ethanol additives) to instigate in situ oil-in-water (O/W) emulsion of heavy oil is presented, for first time, in this paper. Polyvinyl alcohols (PVA) is the world's largest volume synthetic polymer, which has attracted several industrial applications because of its attractive properties including water solubility, surface activeness, chemical and thermal resistance, biocompatibility and biodegradability. In the present study, an experimental setup was developed to investigate tolerance to salinity, thermal stability, and to obtain optimal mixture formulation of PVA and PVA-NaOH (with ethanol additive) for emulsification of heavy oil. Subsequently, coreflooding experiments were performed to compare the recovery performances of water flooding, and those of (0.5%) PVA solution, PVA-NaOH mixture (pH = 12, EtOH = 0) designated PVA(x), and PVA-NaOH mixture (pH = 12, EtOH = 10% v/v) designated PVA(y). The results revealed that the PVA solution was used within 0–70,000 ppm salinity with no significant alteration to its surface activeness and/or emulsification ability. The PVA solution was applied within 25–175 °C with no significant alteration to its effectiveness. Positive synergistic results were obtained from PVA(x), and heavy oil emulsification was enhanced (with higher viscosity reduction) when PVA(y) was applied. By injecting 5.2 PV of PVA(y) (at 70 °C), 83% original oil in place (OOIP) of the highly viscous oil (1.5E + 5 cP at 30 °C) was recovered compared to 73% OOIP and 71% OOIP recovered using PVA(x) and PVA solutions, respectively.
AB - A novel enhanced oil recovery approach using PVA solution and PVA-NaOH mixtures (with ethanol additives) to instigate in situ oil-in-water (O/W) emulsion of heavy oil is presented, for first time, in this paper. Polyvinyl alcohols (PVA) is the world's largest volume synthetic polymer, which has attracted several industrial applications because of its attractive properties including water solubility, surface activeness, chemical and thermal resistance, biocompatibility and biodegradability. In the present study, an experimental setup was developed to investigate tolerance to salinity, thermal stability, and to obtain optimal mixture formulation of PVA and PVA-NaOH (with ethanol additive) for emulsification of heavy oil. Subsequently, coreflooding experiments were performed to compare the recovery performances of water flooding, and those of (0.5%) PVA solution, PVA-NaOH mixture (pH = 12, EtOH = 0) designated PVA(x), and PVA-NaOH mixture (pH = 12, EtOH = 10% v/v) designated PVA(y). The results revealed that the PVA solution was used within 0–70,000 ppm salinity with no significant alteration to its surface activeness and/or emulsification ability. The PVA solution was applied within 25–175 °C with no significant alteration to its effectiveness. Positive synergistic results were obtained from PVA(x), and heavy oil emulsification was enhanced (with higher viscosity reduction) when PVA(y) was applied. By injecting 5.2 PV of PVA(y) (at 70 °C), 83% original oil in place (OOIP) of the highly viscous oil (1.5E + 5 cP at 30 °C) was recovered compared to 73% OOIP and 71% OOIP recovered using PVA(x) and PVA solutions, respectively.
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U2 - 10.1016/j.fuel.2020.119128
DO - 10.1016/j.fuel.2020.119128
M3 - Article
AN - SCOPUS:85091249531
SN - 0016-2361
VL - 285
JO - Fuel
JF - Fuel
M1 - 119128
ER -