pH-Responsive Crude Oil-In-Water Pickering Emulsion Stabilized by Polyacrylamide Nanogels
Abstract
Oil-in-water (o/w) Pickering emulsions stabilized by polyacrylamide (PAM) and poly(acrylamide-co-acrylic acid) nano-sized crosslinked polymeric particles (nanogels) under various conditions are described herein. Nanogels with different crosslinking and charge degree were synthesized through suspension polymerization and characterized at various salinities and pH using dynamic light scattering (DLS) and scanning electron microscopy (SEM). The PAM nanogel-stabilized o/w Pickering emulsions were quickly demulsified in alkaline solutions whereas they showed markedly stability in brines and under acidic conditions. A small amount of nanogels were sufficient for the formation of Pickering emulsions. The average diameter of oil droplets was no longer decreasing with nanogel concentration increment above 1000 mg/L. In addition, the average diameter of oil drops was independent of sonication period in the range of 15-240 s. Interestingly, the string-like structures of nanogel aggregations were found in the aromatic hydrocarbons/water Pickering emulsions, which significantly enhanced the emulsion stability. Compared to the crude oil, the corresponding Pickering emulsions showed excellent flowability at various shear rates. The crude oil/water Pickering emulsions could be broken using alkali as a trigger, which suggests the potential utility for the recovery of crude oil.
Recommended Citation
J. Geng et al., "pH-Responsive Crude Oil-In-Water Pickering Emulsion Stabilized by Polyacrylamide Nanogels," Fuel, vol. 258, Elsevier Ltd, Dec 2019.
The definitive version is available at https://doi.org/10.1016/j.fuel.2019.116159
Department(s)
Geosciences and Geological and Petroleum Engineering
Second Department
Chemistry
Research Center/Lab(s)
Center for Research in Energy and Environment (CREE)
Keywords and Phrases
Enhanced oil recovery; Nanogel; Pickering emulsion
International Standard Serial Number (ISSN)
0016-2361
Document Type
Article - Journal
Document Version
Citation
File Type
text
Language(s)
English
Rights
© 2019 Elsevier Ltd, All rights reserved.
Publication Date
01 Dec 2019
Comments
The authors would like to express their grateful acknowledgement to the financial support from DOE under the contract of DE-FE0024558.