TY - JOUR

T1 - Modified Langmuir-Hinselwood kinetics for dynamic adsorption of surfactants at the air/water interface

AU - Chang, C. H.

AU - Franses, E. I.

N1 - Funding Information:
WC are grateful to the Whitaker Foundation for Biomedical Research and to the National Science Foundation (grant ,!,t EXCS9 1-12154) for particl support of this work. We also thank Professors J. Talbot and N.-H-L. Wang for helpful discussions.

PY - 1992/12/11

Y1 - 1992/12/11

N2 - The Langmuir-Hinselwood (L-H) equation is the simplest kinetic equation which is consistent with Langmuir's equilibrium isotherm. This kinetic equation cannot describe well the dynamic surface tension data for octanol, sodium dodecyl sulfate (SDS), and other surfactants. A new kinetic equation for the rate of adsorption from the subsurface (dl/dt = kaLc(θ,t)(1-θ) exp(-Bθ)-kdL Γ exp(-Bθ). where θ is the fractional surface coverage Γ/Γm, c(θ,t) is the subsurface concentration, and kaL, kdL, and B are constants) includes modification of the kinetics but not of the equilibrium isotherm. The new equation describes better the capture efficiency of the interfacial monolayer for additional surfactant, and can describe activation barriers for adsorption and desorption, or cooperative adsorption caused by primarily attractive interactions between the monolayer and the dissolved surfactant. This equation was used in a new model of mixed kinetics for one-dimensional diffusion/adsorption/desorption. For octanol and heptanol, the initial adsorption rate is controlled by intrinsic adsorption/desorption kinetics (slow adsorption/desorption). With increasing surface coverage, dynamic adsorption gets closer to the diffusion-controlled limit (fast adsorption/desorption relative to diffusion). This indicates attractive and cooperative interactions of alcohol molecules in the monolayer. For sodium di-2-ethylhexylsulfosuccinate (DESS or AOT) and SDS, adsorption is much slower than predicted by diffusion-controlled models. The modified L-H equation in a mixed-kinetics model can fit the data well. The capture efficiency factor, kaL exp(-bθ), increases with increasing SDS concentration cSDS or NaCl concentration cs, indicating that adsorption is strongly affected by electrostatic barriers. For cs = 0 and cSDS = 1.7 to 5.9 mM (for θc<0.4), the estimated surface electrical potential is in the range 150-230 mV, and is consistent with classical double-layer theory. For θc > 0.4 and a high salt concentration, the parameter B may involve substantial steric or other interactions.

AB - The Langmuir-Hinselwood (L-H) equation is the simplest kinetic equation which is consistent with Langmuir's equilibrium isotherm. This kinetic equation cannot describe well the dynamic surface tension data for octanol, sodium dodecyl sulfate (SDS), and other surfactants. A new kinetic equation for the rate of adsorption from the subsurface (dl/dt = kaLc(θ,t)(1-θ) exp(-Bθ)-kdL Γ exp(-Bθ). where θ is the fractional surface coverage Γ/Γm, c(θ,t) is the subsurface concentration, and kaL, kdL, and B are constants) includes modification of the kinetics but not of the equilibrium isotherm. The new equation describes better the capture efficiency of the interfacial monolayer for additional surfactant, and can describe activation barriers for adsorption and desorption, or cooperative adsorption caused by primarily attractive interactions between the monolayer and the dissolved surfactant. This equation was used in a new model of mixed kinetics for one-dimensional diffusion/adsorption/desorption. For octanol and heptanol, the initial adsorption rate is controlled by intrinsic adsorption/desorption kinetics (slow adsorption/desorption). With increasing surface coverage, dynamic adsorption gets closer to the diffusion-controlled limit (fast adsorption/desorption relative to diffusion). This indicates attractive and cooperative interactions of alcohol molecules in the monolayer. For sodium di-2-ethylhexylsulfosuccinate (DESS or AOT) and SDS, adsorption is much slower than predicted by diffusion-controlled models. The modified L-H equation in a mixed-kinetics model can fit the data well. The capture efficiency factor, kaL exp(-bθ), increases with increasing SDS concentration cSDS or NaCl concentration cs, indicating that adsorption is strongly affected by electrostatic barriers. For cs = 0 and cSDS = 1.7 to 5.9 mM (for θc<0.4), the estimated surface electrical potential is in the range 150-230 mV, and is consistent with classical double-layer theory. For θc > 0.4 and a high salt concentration, the parameter B may involve substantial steric or other interactions.

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U2 - 10.1016/0166-6622(92)80230-Y

DO - 10.1016/0166-6622(92)80230-Y

M3 - Article

AN - SCOPUS:44049112366

VL - 69

SP - 189

EP - 201

JO - Colloids and Surfaces

JF - Colloids and Surfaces

SN - 0166-6622

IS - 2-3

ER -