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Received June 5, 2016
Accepted November 20, 2016
- This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Effect of hydrophobic modification on the structure and rheology of aqueous and brine solutions of scleroglucan polymer
Department of Polymer Reactions Engineering, Faculty of Chemical Engineering, Tarbiat Modares University, 14155-143, Tehran, Iran 1Chemicals, Polymers & Petrochemicals Technology Development Division, Research Institute of Petroleum Industries (RIPI), 14665-137, Tehran, Iran
asharif@modares.ac.ir
Korean Journal of Chemical Engineering, March 2017, 34(3), 903-912(10), 10.1007/s11814-016-0322-0
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Abstract
Amphiphilic scleroglucans were synthesized by grafting hydrophobic stearate groups in various densities onto the polysaccharide under its triple-helix conformation. Furthermore, a polyelectrolyte was obtained by attaching ionic-sulfonic groups to the hydrophobically modified scleroglucan. Rheological measurements demonstrated the role of grafted stearates in helix-coil transition of scleroglucan and in reducing the viscosity of scleroglucan in pure aqueous and brine solutions. Nevertheless, grafting the ionic-sulfonic groups caused a substantial recovery of the lost viscosity, especially in brine solution at 90 °C, while keeping the amphiphilic character of the hydrophobically modified scleroglucan. Additionally, the hydrophobic modification altered the adsorption behavior of scleroglucan on oil-reservoir rock surfaces: the higher the grafting density, the greater the adsorption amount. However, the polyelectrolyte sample showed the lowest adsorption among all modified samples. Finally, the modified scleroglucans are promising candidates for enhanced oil recovery applications.
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References
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Babu K, Pal N, Saxena VK, Mandal A, Korean J. Chem. Eng., 33(2), 711 (2016)
Sodeifian G, Daroughegi R, Aalaie J, Korean J. Chem. Eng., 32(12), 2484 (2015)
Chai W, Zhang Y, Hou Y, Polym. Chem., 4, 1006 (2013)
Chichkanov SV, Proskurina VE, Myagchenkov VA, Chemistry and Computational Simulation. Butlerov Communications., 3, 33 (2002)
Pierce DS, Mechanics of Impression Evidence., CRC Press (2011).
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Aalaie J, Hemmati M, Sajjadian VA, J. Macromol. Sci.-Phys., 51, 2473 (2012)
Kulicke WM, Lettau AI, Thielking H, Carbohydr. Res., 297, 135 (1997)
Zatz JL, Knapp S, J. Pharm. Sci., 73, 468 (1984)
Alquraishi AA, Alsewailem FD, Carbohydr. Polym., 88, 859 (2012)
Lee BB, Ravindra P, Chan ES, Colloids Surf. A: Physicochem. Eng. Asp., 332, 112 (2009)
Docoslis A, Giese RF, van Oss CJ, Colloids Surf. B: Biointerfaces, 19, 147 (2000)
Nahringbauer I, J. Colloid Interface Sci., 176(2), 318 (1995)
Brunchi C, Bercea M, Morariu S, Dascalu M, J. Polym. Res., 23, 123 (2016)
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