Salinity, pH , and Surfactant Concentration Effects on CO2-Foam

Author(s):  
Yi Liu ◽  
R.B. Grigg ◽  
Baojun Bai
2012 ◽  
Vol 116 (3) ◽  
pp. 987-991 ◽  
Author(s):  
Arben Jusufi ◽  
David N. LeBard ◽  
Benjamin G. Levine ◽  
Michael L. Klein

2021 ◽  
Author(s):  
Amit Katiyar ◽  
Troy Knight ◽  
Adam Grzesiak ◽  
Pete Rozowski ◽  
Quoc Nguyen

Abstract Several gas Enhanced Oil Recovery (EOR) pilots enhanced with aqueous-foam based conformance solutions have been implemented in the last 30 years. While these pilots were technically successful, there were economic challenges limiting their commercial viability. Many of these pilots were implemented with water-soluble foaming surfactants that can get adversely affected by near wellbore gas-water gravity segregation and adsorption loss up to 90% of the injected surfactant. Novel, gas-soluble surfactants can be injected with the gas phase where these surfactants are carried with the gas to thief zones faster and deeper with relatively lower adsorption to the rock surface. However, the conventional foam modeling approach relied only on the surfactant concentration in brine to determine foam strength, which adversely predicted the performance of gas soluble surfactants. With proven laboratory evaluations and multiple successful field implementations, the advantages of low adsorbing and gas soluble surfactants cannot be ignored. In this paper, the advantages of surfactant partitioning to the gas phase are confirmed by correcting the conventional foam modeling approach while simulating 1D transport of CO2-foam displacing brine in porous media. An empirical foam model was developed from the lab scale core flooding work of CO2foam transport through porous media using a novel gas-soluble foaming surfactant. While investigating the performance of gas soluble surfactants, global surfactant concentration was used to determine foam strength as the surfactant can transport to the gas-water interface from both the phases. Lab experiments and simulations with an improved foam modeling approach confirmed that a higher gas phase partitioning surfactant generated robust foam and deeper foam propagation while injecting surfactant with CO2in a water saturated core. In addition, comparing three partition coefficient scenarios around 1 on mass basis, the higher gas phase partitioning surfactant showed the larger delay in gas breakthrough. Overall, the simulation results with our better modeling approach do support the advantages of the higher gas phase surfactant partitioning in deeper foam transport and conformance enhancement for the gas-EOR technology.


2002 ◽  
Vol 35 (18) ◽  
pp. 6915-6919 ◽  
Author(s):  
Gaofeng Pan ◽  
E. David Sudol ◽  
Victoria L. Dimonie ◽  
Mohamed S. El-Aasser

2005 ◽  
Vol 54 (6) ◽  
pp. 875-881 ◽  
Author(s):  
Ajit Ranade ◽  
Nandika D'Souza ◽  
Christopher Thellen ◽  
Jo Ann Ratto

Energies ◽  
2017 ◽  
Vol 10 (12) ◽  
pp. 1970 ◽  
Author(s):  
Shehzad Ahmed ◽  
Khaled Elraies ◽  
Muhammad Hashmet ◽  
Alvinda Hanamertani

Pharmaceutics ◽  
2021 ◽  
Vol 13 (8) ◽  
pp. 1287
Author(s):  
Vladimir Katev ◽  
Sonya Tsibranska-Gyoreva ◽  
Zahari Vinarov ◽  
Slavka Tcholakova

Lipid-based formulations (LBF) enhance oral drug absorption by promoting drug solubilization and supersaturation. The aim of the study was to determine the effect of the lipid carrier type, drop size and surfactant concentration on the rate of fenofibrate release in a bicarbonate-based in vitro digestion model. The effect of the lipid carrier was studied by preparing type I LBF with drop size ≈ 2 µm, based on medium-chain triglycerides (MCT), sunflower oil (SFO), coconut oil (CNO) and cocoa butter (CB). The drop size and surfactant concentration effects were assessed by studying MCT and SFO-based formulations with a drop size between 400 nm and 14 µm and surfactant concentrations of 1 or 10%. A filtration through a 200 nm filter followed by HPLC analysis was used to determine the aqueous fenofibrate, whereas lipid digestion was followed by gas chromatography. Shorter-chain triglycerides were key in promoting a faster drug release. The fenofibrate release from long-chain triglyceride formulations (SFO, CNO and CB) was governed by solubilization and was enhanced at a smaller droplet size and higher surfactant concentration. In contrast, supersaturation was observed after the digestion of MCT emulsions. In this case, a smaller drop size and higher surfactant had negative effects: lower peak fenofibrate concentrations and a faster onset of precipitation were observed. The study provides new mechanistic insights on drug solubilization and supersaturation after LBF digestion, and may support the development of new in silico prediction models.


2009 ◽  
Vol 283-284 (1) ◽  
pp. 34-44 ◽  
Author(s):  
Hugo Martínez-Gutiérrez ◽  
Víctor M. Ovando-Medina ◽  
René D. Peralta

2021 ◽  
Vol 409 ◽  
pp. 126878
Author(s):  
M. Vijayanand ◽  
R. Varahamoorthi ◽  
P. Kumaradhas ◽  
S. Sivamani ◽  
Mithun V. Kulkarni

2017 ◽  
Vol 101 ◽  
pp. 02008
Author(s):  
Widia Yanti ◽  
Sugiatmo Kasmungin ◽  
Rabiatul Adawiyah ◽  
Blandina Kolanus

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