Tween 20 system studies

Kunieda s group reported numerous viscoelastic worm-like micellar systems in the salt-free condition when a lipophilic nonionic surfactant such as short hydrophilic chain poly(oxyethylene) alkyl ether, C EOni, or N-hydroxyethyl-N-methylaUcanolamide, NMEA-n, was added to the dilute micellar solution of hydrophilic cationic (dodecyltrimethylammonium bromide, DTAB and hexade-cyltrimethylammonium bromide, CTAB) [12-14], anionic (sodium dodecyl sulfate, SDS [15, 16], sodium dodecyl trioxyethylene sulfate, SDES [17], and Gemini-type [18]) or nonionic (sucrose alkanoates, C SE [9, 19], polyoxyethylene cholesteryl ethers, ChEO [10, 20], polyoxyethylene phytosterol, PhyEO [11, 21] and polyoxyethylene sorbitan monooleate, Tween-80 [22]) surfactants. The mechanism of formation of these worm-Hke stmctures and the resulting rheological behavior of micellar solutions is discussed in this section based in some actual published and unpublished results, but conclusions can qualitatively be extended to aU the systems studied by Kunieda s group. 

Chromobacterium viscosum AOT/Tween 85 mixed micellar system Activity studies [84]... 

Previous work has shown that binary surfactant systems containing Dowfax 8390 and the branched hydrophobic surfactant AOT can form Winsor III systems with both PCE and decane whereas DOWFAX 8390 by itself cannot (Wu et. al. 1999). This binary surfactant system was used in conjunction with hydrophobic octanoic acid to help with phase behavior and lessen the required concentration of CaCl2. Since this formulation is rather complicated, questions about field robustness arise. Thus, for the phase behavior studies presented here, we used the simple binary system of the nonionic TWEEN 80 and the branched hydrophobic AOT, and we optimized the NaCl concentration to give the Winsor Type III system. The lesser electrolyte concentration requirement for the binary TWEEN 80/ AOT system helps to decrease the potential for undesirable phase behavior such as surfactant precipitation, thereby increasing surfactant system robustness. 

The overall objective of this research was to evaluate the effects of cosolvent addition on the ability of an ethoxylated nonionic surfactant to recover PCE from a heterogeneous, 2-D system. The specific tasks of this work were to (a) quantify the PCE solubilization rate and capacity in the presence and absence of a representative cosolvent (EtOH) and (b) investigate the effects of EtOH addition on surfactant delivery, plume migration and PCE recovery in a 2-D, layered sand tank. A representative nonionic surfactant, polyoxyethylated (POE) (20) sorbitan monooleate (Tween 80), was selected for study because of its capacity to solubilize PCE ( 0.7 g PCE/g surf at 20°C) and relatively high interfacial tension with PCE (5 dynes/cm). EtOH was chosen as the representative cosolvent because of its relatively low density (p = 0.79 g/cm1) and regulatory acceptance. 

Analysis of Tween 80 was performed using a Hewlett Packard 1100 series HPLC equipped with a Sedex 55 Evaporative Light Scattering Detector (ELSD). The mobile phase consisted of 80% acetonitrile and 20% water. Duplicate injections (5 pL) of each sample were evaluated by HPLC. Potassium iodide, used for the 1-D column and 2-D box tracer studies, was analyzed with a continuous flow Isco V4 variable UV wavelength absorbance detector equipped with an EZChrom Chromatography data acquisition system. 

Copolymerization. Tailor-made -functionalized polymers structurally related to the host polymer may be synthesized by copolymerization of functionalized monomers with properly selected conventional monomers. Copolymerization parameters may differ markedly between various monomer couples. The concentration of the built-in -fiinctionalized units can be controlled by the concentration ratio of selected reactants [46]. Systems differing in the structure of their backbones, distribution and attachment modes of functionalized moieties are thus available and may serve as polymer stabilizers as well as suitable materials for more profound mechanistic studies of relations l tween activity, persistency and physical properties of the system additive/polymer matrix. Improvement of the compatibility with the host polymer, formation of polymers from functionalized monomers that do not homopolymerize, and polymeric stabilizers containing a proper combination of two functional groups forming cooperative systems in one molecule may be considered as the most valuable properties of copolymeric stabilizers. 

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