4.6 Article

Contamination in Sodium Dodecyl Sulfate Solutions: Insights from the Measurements of Surface Tension and Surface Rheology

Journal

LANGMUIR
Volume 38, Issue 23, Pages 7179-7189

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.langmuir.2c00460

Keywords

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Funding

  1. National Science Foundation [CBET-1934513]
  2. American Chemical Society Petroleum Research Fund [61617-DNI9]

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The presence of contamination, such as dodecanol (LOH), in sodium dodecyl sulfate (SDS) solutions significantly affects interfacial properties. The addition of an electrolyte can lead to misinterpretation of surface purity based on surface tension isotherms. This study estimated the amount of dodecanol in SDS solutions and predicted the viscoelasticity of surfactant-laden surfaces using a rheological model.
The presence of contamination in sodium dodecyl sulfate (SDS) solutions in the form of dodecanol (LOH) is known to drastically affect the resulting interfacial properties such as surface tension (SFT) and rheology. Dodecanol molecules, which are the product of SDS hydrolysis and are inherently present in SDS solutions, have higher surface activity compared to SDS because they are less soluble in water. A characteristic dip in the SFT isotherm is an indicator of the dodecanol contamination in the sample. The presence of an electrolyte in the solution impacts the surface activity of SDS and its critical micelle concentration, and could yield SFT isotherms that closely match those obtained for pure SDS samples. The interpretation of the isotherms in such cases could thus lead to misinterpretation of the surface purity. In this work, we have examined the SFT isotherms for SDS solutions in both the absence and presence of electrolyte. We have fitted the isotherms to three different thermodynamic adsorption models to estimate the amount of dodecanol present in the sample. We have applied the estimated values for the LOH content in a two-component rheological model to predict the viscoelasticity of such surfactant-laden surfaces. We have compared these results with the experimentally measured interfacial rheological properties. Our findings demonstrate that the presence of impurities can be captured under dynamic expansion and contractions, even for solutions containing background electrolyte.

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