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Adsorption of Surface Active Ionic Liquids on Different Rock Types under High Salinity Conditions
A new class of surface active ionic liquids (SAIL) have been reported to be a greener alternative to the conventional surfactants in enhanced oil recovery (EOR). These SAILs work efficiently under harsh salinity conditions encountered in the reservoir thereby recovering more additional oil during th...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6791850/ https://www.ncbi.nlm.nih.gov/pubmed/31611581 http://dx.doi.org/10.1038/s41598-019-51318-2 |
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author | Nandwani, Shilpa Kulbhushan Chakraborty, Mousumi Gupta, Smita |
author_facet | Nandwani, Shilpa Kulbhushan Chakraborty, Mousumi Gupta, Smita |
author_sort | Nandwani, Shilpa Kulbhushan |
collection | PubMed |
description | A new class of surface active ionic liquids (SAIL) have been reported to be a greener alternative to the conventional surfactants in enhanced oil recovery (EOR). These SAILs work efficiently under harsh salinity conditions encountered in the reservoir thereby recovering more additional oil during the tertiary oil recovery process. Adsorption mechanism of SAILs on different rock surface is however, not yet reported in the literature. This article highlights adsorption mechanism of three cationic SAILs having different headgroups, viz., imidazolium, pyridinium, pyrrolidinium, on different rock surfaces (crushed natural carbonate rock and crushed sandstone rock). All the SAILs studied here however had the same tail length and same anion (Br(−)) attached to it. XRD and XPS characterization techniques reveal that the crushed natural carbonate rock contains a substantial amount of silica, thus rendering it a slight negative charge. Static adsorption tests show that the retention efficiency on the natural carbonate type of rock for all the SAILs was lower than the conventional cationic surfactant, CTAB. The adsorption data obtained thereby was examined using four different adsorption isotherm models (Langmuir, Freundlich, Redlich-Peterson, and Sips). Results suggest that Sips adsorption isotherm model can satisfactorily estimate the adsorption of all the surface active agents on the natural carbonate rock. Factors like mineralogical composition of rock surface, presence of divalents, temperature, and structure of surfactants strongly affect the amount of surfactant adsorbed on reservoir rock. In order to evaluate the simultaneous effect all these factors as well as their interdependence on the retention capability of the three SAILs, a design of experiments approach has been employed further in this study. Statistical analysis of the data obtained after performing the full factorial experiments reveal that at high salinity, imidazoluim based SAIL show minimal adsorption on crushed natural carbonate rock at higher temperature. In general, at a given ionic strength, with increasing temperature as the amount of divalent in the aqueous solution increases, the amount of SAIL adsorbed on both the rock types decreases. Electrostatic attraction is the basic mechanism in governing adsorption of SAILs on the two types of rock surfaces. Results presented in this work can be used for EOR schemes. |
format | Online Article Text |
id | pubmed-6791850 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67918502019-10-21 Adsorption of Surface Active Ionic Liquids on Different Rock Types under High Salinity Conditions Nandwani, Shilpa Kulbhushan Chakraborty, Mousumi Gupta, Smita Sci Rep Article A new class of surface active ionic liquids (SAIL) have been reported to be a greener alternative to the conventional surfactants in enhanced oil recovery (EOR). These SAILs work efficiently under harsh salinity conditions encountered in the reservoir thereby recovering more additional oil during the tertiary oil recovery process. Adsorption mechanism of SAILs on different rock surface is however, not yet reported in the literature. This article highlights adsorption mechanism of three cationic SAILs having different headgroups, viz., imidazolium, pyridinium, pyrrolidinium, on different rock surfaces (crushed natural carbonate rock and crushed sandstone rock). All the SAILs studied here however had the same tail length and same anion (Br(−)) attached to it. XRD and XPS characterization techniques reveal that the crushed natural carbonate rock contains a substantial amount of silica, thus rendering it a slight negative charge. Static adsorption tests show that the retention efficiency on the natural carbonate type of rock for all the SAILs was lower than the conventional cationic surfactant, CTAB. The adsorption data obtained thereby was examined using four different adsorption isotherm models (Langmuir, Freundlich, Redlich-Peterson, and Sips). Results suggest that Sips adsorption isotherm model can satisfactorily estimate the adsorption of all the surface active agents on the natural carbonate rock. Factors like mineralogical composition of rock surface, presence of divalents, temperature, and structure of surfactants strongly affect the amount of surfactant adsorbed on reservoir rock. In order to evaluate the simultaneous effect all these factors as well as their interdependence on the retention capability of the three SAILs, a design of experiments approach has been employed further in this study. Statistical analysis of the data obtained after performing the full factorial experiments reveal that at high salinity, imidazoluim based SAIL show minimal adsorption on crushed natural carbonate rock at higher temperature. In general, at a given ionic strength, with increasing temperature as the amount of divalent in the aqueous solution increases, the amount of SAIL adsorbed on both the rock types decreases. Electrostatic attraction is the basic mechanism in governing adsorption of SAILs on the two types of rock surfaces. Results presented in this work can be used for EOR schemes. Nature Publishing Group UK 2019-10-14 /pmc/articles/PMC6791850/ /pubmed/31611581 http://dx.doi.org/10.1038/s41598-019-51318-2 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Nandwani, Shilpa Kulbhushan Chakraborty, Mousumi Gupta, Smita Adsorption of Surface Active Ionic Liquids on Different Rock Types under High Salinity Conditions |
title | Adsorption of Surface Active Ionic Liquids on Different Rock Types under High Salinity Conditions |
title_full | Adsorption of Surface Active Ionic Liquids on Different Rock Types under High Salinity Conditions |
title_fullStr | Adsorption of Surface Active Ionic Liquids on Different Rock Types under High Salinity Conditions |
title_full_unstemmed | Adsorption of Surface Active Ionic Liquids on Different Rock Types under High Salinity Conditions |
title_short | Adsorption of Surface Active Ionic Liquids on Different Rock Types under High Salinity Conditions |
title_sort | adsorption of surface active ionic liquids on different rock types under high salinity conditions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6791850/ https://www.ncbi.nlm.nih.gov/pubmed/31611581 http://dx.doi.org/10.1038/s41598-019-51318-2 |
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