1981
DOI: 10.1016/0021-9797(81)90093-x
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Three-dimensional phase diagrams and interfacial tensions of the water—dodecane—pentanol—sodium octylbenzene sulfonate system

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Cited by 41 publications
(7 citation statements)
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“…γ ow decreases with salinity until reaching a minimum value at optimum salinity (i.e., near HLD = 0). Bellocq et al studied how γ ow , γ om , and γ mw change as a function of the active surfactant concentration for a surfactant–alcohol–oil–brine system, finding behavior similar to that described above except for changes in salinity. Kunieda and Shinoda also found similar behavior for γ ow , γ om , and γ mw as a function of temperature.…”
Section: Introductionmentioning
confidence: 63%
“…γ ow decreases with salinity until reaching a minimum value at optimum salinity (i.e., near HLD = 0). Bellocq et al studied how γ ow , γ om , and γ mw change as a function of the active surfactant concentration for a surfactant–alcohol–oil–brine system, finding behavior similar to that described above except for changes in salinity. Kunieda and Shinoda also found similar behavior for γ ow , γ om , and γ mw as a function of temperature.…”
Section: Introductionmentioning
confidence: 63%
“…The volume in which three phases are in equilibrium close to the condition R = 1, which is called the three phase body, has a strange shape as illustrated in the lower left part of Fig. 2, and shown in various ways elsewhere [14][15][16], even in quaternary SOWA systems with an alcohol co-surfactant [17]. An outstanding analysis of the body volume of a three liquid phase equilibrium is available elsewhere [18], although the reported quaternary system does not contain any surfactant.…”
Section: Three-phase Behavior Zonementioning
confidence: 99%
“…For ethoxylated nonionics, the scanning variables used most are the temperature and the average ethylene oxide number (EON) in the head group. For any type of surfactant, the ACN has been also used as the scanning variable, although the actual liquid range (5)(6)(7)(8)(9)(10)(11)(12)(13)(14)(15)(16) for n-alkanes is rather small as far as a physicochemical change is concerned. In effect, it will be shown later that the full experimental range of ACN for liquid n-alkanes (5-16) is, for ethoxylated nonionics, equivalent to a change in about 1.5 EO groups in the polyether head or 30°C in temperature variation, and for anionics to a change in salinity from 1 to 5 wt% NaCl.…”
Section: Empirical Correlations To Attain Optimum Formulationmentioning
confidence: 99%
“…More hydrophilic ones have a very small effect, while more lipophilic ones like n-pentanol or n-hexanol contribute to the hydrophilicity-lipophilicity balance at interface and result in a formulation effect included as the term called f(A) or /(A) in the SAD/HLD equations discussed in Part 1 of this review [1] or equivalent way to take into account the alcohol effect [28,33,37,39,55,[137][138][139][140][141][142]]. This f(A)//(A) term is easy to measure, but it has not been reported with accuracy in the literature for two reasons.…”
Section: Alcohol Effects As Cosurfactantsmentioning
confidence: 99%