Asphaltene Adsorption onto Self-Assembled Monolayers of Mixed Aromatic and Aliphatic Trichlorosilanes

Published

June 2, 2009

Author(s)

Daniel A. Fischer, Saloman Turgman-Cohen, Mathew Smith, P K. Kilpatrick, Jan Genzer

Abstract

The adsorption of asphaltenes onto flat solid surfaces modified with mixed self-assembled monolayers (SAMs) of aliphatic and aromatic trichlorosilanes with varying wettabilities, aromaticities, and thicknesses is tested. The mixed SAMs are characterized by means of contact angle to assess hydrophobicity and molecular and chemical uniformity, spectroscopic ellipsometry to measure the thickness of the films, and near edge x-ray absorption fine structure (NEXAFS) spectroscopy to assess chemical and molecular composition. The molecular characteristics of the adsorbed asphaltene layer and the extent of asphaltene adsorption are determined using NEXAFS and spectroscopic ellipsometry, respectively. The SAMs are formed by depositing phenyl-, phenethyl-, butyl- and octadecyl- trichlorosilanes from toluene solutions onto silica-coated substrates; the chemical composition and the wettability of the SAM surface is tuned systematically by varying the trichlorosilane composition in the deposition solutions. The adsorption of asphaltenes on the substrates does not correlate strongly with the SAM chemical composition. Instead, the extent of asphaltene adsorption decreases with increasing SAM thickness. This observation suggests that the leading interaction governing the adsorption of asphaltenes is their interaction with the polar silica substrate and that the chemical composition of the SAM is of secondary importance.

Citation

Langmuir

Volume

25

Issue

11

Pub Type

Journals

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Keywords

Asphaltene, Trichlorosilanes, SAMS, NEXAFS

Citation

Fischer, D. , Turgman-Cohen, S. , Smith, M. , Kilpatrick, P. and Genzer, J. (2009), Asphaltene Adsorption onto Self-Assembled Monolayers of Mixed Aromatic and Aliphatic Trichlorosilanes, Langmuir, [online], https://tsapps.nist.gov/publication/get_pdf.cfm?pub_id=902377 (Accessed December 5, 2024)