Influence of ionic strength on complex formation between poly(ethylene oxide) and cationic surfactant and turbulent wall shear stress in aqueous ... article from: Chemical Engineering Journal] Buy on Amazon

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Influence of ionic strength on complex formation between poly(ethylene oxide) and cationic surfactant and turbulent wall shear stress in aqueous ... article from: Chemical Engineering Journal]

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PublisherElsevier
ISBN / ASINB000PDTZLC
ISBN-13978B000PDTZL2
AvailabilityAvailable for download now
MarketplaceUnited States  🇺🇸

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This digital document is a journal article from Chemical Engineering Journal, published by Elsevier in 2007. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.

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We investigate the influence of ionic strength on the interaction between poly(ethylene oxide) (PEO) and cationic surfactant, hexadecyltrimethylammonium chloride (HTAC), and the consequent effect on turbulent drag reduction in aqueous PEO/HTAC solutions. Conductivity and surface tension data for PEO-HTAC in aqueous solution indicate that salt stabilizes binding of HTAC micelles to the polymer. Dynamic light scattering analysis indicates an increase in hydrodynamic radius for HTAC micelles in aqueous salt solution. In contrast, salt reduces the hydrodynamic radius of PEO-HTAC complexes. The latter observation is consistent with contraction of the PEO-HTAC complex via electrostatic screening. For the measurement of turbulent drag reduction in a Couette cell, our data indicate that the minimum wall shear stress in aqueous HTAC solutions occurs at an optimum HTAC concentration, close to CMC, and this optimum concentration value decreases with increasing ionic strength. This result suggests a lowering of the CMC in turbulent flow. For aqueous PEO-HTAC mixtures, the minimum wall shear stress occurs at an optimum PEO concentration smaller than that of pure PEO solutions, and this optimum concentration value increases with ionic strength. Our findings provide evidences that the turbulent wall shear stress does not always scale inversely with the hydrodynamic volume of the polymer-surfactant complex.
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