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Journal ArticleDOI

Surface structure of cationic surfactant solutions investigated by angular resolved X‐ray photoelectron spectroscopy with calibrated transmission function

Chuangye Wang, +1 more
- 01 Apr 2011 - 
- Vol. 43, Iss: 4, pp 784-790
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TLDR
In this article, the surface structure of cationic surfactant solutions by angular resolved X-ray photoelectron spectroscopy (ARXPS) after calibrating transmission function of the spectrometer was investigated.
Abstract
The main goal of the present work is to investigate the surface structure of cationic surfactant solutions by angular resolved X-ray photoelectron spectroscopy (ARXPS) after calibrating transmission function of the spectrometer. We have estimated the transmission function of the ARXPS spectrometer, and with it, we investigated solution of tetrabutylammonium iodide in a nonaqueous polar solvent. By genetic algorithm, the fractional concentration-depth profiles of constituents were reconstructed. These depth profiles evidence the enrichment of surfactant and the depletion of solvent in the surface regime and verify the separate distributions of oppositely charged surfactant ions. From those profiles we draw a conclusion that there is a preferred orientation for cation present at the surface, and the possibility for cation to take this orientation is related to its surface amount. Copyright © 2010 John Wiley & Sons, Ltd.

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Citations
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Core level photoelectron spectroscopy of heterogeneous reactions at liquid–vapor interfaces: Current status, challenges, and prospects

TL;DR: X-ray photoelectron spectroscopy is an excellent method for the investigation of these interfaces due to its surface sensitivity, elemental and chemical specificity, and the possibility to obtain information on the depth distribution of solute and solvent species in the interfacial region as discussed by the authors.
Journal ArticleDOI

Surfactant-promoted reactions of Cl2 and Br2 with Br- in glycerol.

TL;DR: In this paper, gas-liquid scattering experiments are used to explore reactions of gaseous Cl2 and Br2 with a 0.03 M solution of the surfactant tetrahexylammonium bromide (THABr) dissolved in glycerol.
Journal Article

Surfactant-Promoted Reactions of Cl2 and Br2 with Br– in Glycerol B

TL;DR: The THA(+) ion appears to be a powerful interfacial catalyst for promoting reaction of Cl2 and Br2 with Br(-) and for ferrying the resultant ions into solution.
References
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Empirical atomic sensitivity factors for quantitative analysis by electron spectroscopy for chemical analysis

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Molecular bonding and interactions at aqueous surfaces as probed by vibrational sum frequency spectroscopy.

TL;DR: Her research group uses a combination of linear and nonlinear optical methods, thermodynamic measurements, and theory to characterize interactions at aqueous surfaces, metal and semiconductor surfaces in contact with liquids and adsorbates, and liquid/liquid interfaces.
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Photoionization cross sections and photoelectron angular distributions for x-ray line energies in the range 0.132–4.509 keV targets: 1 ≤ Z ≤ 100

TL;DR: In this article, the relativistic self-consistent Dirac-Slater potentials were used to calculate the photoionization cross-sections and asymmetry parameters of photoelectrons for 14 incident photon energies corresponding to x-ray lines in the energy range 0.132-4.509 keV.
Journal ArticleDOI

Attenuation of photoelectrons in monolayers of n-alkanethiols adsorbed on copper, silver, and gold

TL;DR: In this paper, the relationship between tr and the kinetic energy of photoelectrons, over the energy range studied by using SAMs, can be fit equally well by the expressions \ = 9.0 * 0.022K8 or tr o KEp where p = 0.67 + 0.11.
Journal ArticleDOI

Liquid–liquid interfaces: studied by X-ray and neutron scattering

TL;DR: In this paper, the first precise measurements of interfacial widths at water-oil interfaces and the ordering of surfactants adsorbed to these interfaces were obtained, and phase transitions and domain formation in surfactant monolayers were studied.
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