2004
DOI: 10.1016/j.jcis.2003.08.006
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Thermodynamic method for prediction of surfactant-modified oil droplet contact angle

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Cited by 21 publications
(18 citation statements)
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“…where K D is the MB partition coefficient (mol·mol −1 ), ΔH is adsorption enthalpy change (J·mol −1 ), T is temperature (K), ΔS is adsorption entropy change (J·K −1 ·mol −1 ), and ΔG is Gibbs free energy change (J·mol −1 ) [31][32][33].…”
Section: Adsorption Thermodynamicsmentioning
confidence: 99%
“…where K D is the MB partition coefficient (mol·mol −1 ), ΔH is adsorption enthalpy change (J·mol −1 ), T is temperature (K), ΔS is adsorption entropy change (J·K −1 ·mol −1 ), and ΔG is Gibbs free energy change (J·mol −1 ) [31][32][33].…”
Section: Adsorption Thermodynamicsmentioning
confidence: 99%
“…The enthalpy is dependent on the volume of the adsorbed phase because initially the volume of the adsorbed phase is zero [24]. These approximations were applied to the adsorption from aqueous solutions of organic substances [8,15,[25][26][27][28].…”
Section: Thermodynamic Parametersmentioning
confidence: 99%
“…The enthalpy depends on the volume of the adsorbed phase because initially the volume of the adsorbed phase is zero [25]. These approximations were applied to the adsorption of organic substances [26][27][28][29] from aqueous solutions. Thus, we will approximate the differential or molar enthalpy in the solution ( h a ) as shown in the equation…”
Section: Thermodynamic Parametersmentioning
confidence: 99%