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Effect of Alkyl Chain Length on Carboxylic Acid SAMs on Ti-6Al-4V

The formation of methyl-terminated carboxylic acid self-assembled monolayers (SAMs) with even numbers of carbons, from eighteen to thirty, was investigated on the oxide surface of Ti-6Al-4V and component metal oxides. Modified surfaces were characterized using diffuse reflectance infrared Fourier tr...

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Detalles Bibliográficos
Autores principales: Buckholtz, Gavin A., Gawalt, Ellen S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5448898/
http://dx.doi.org/10.3390/ma5071206
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author Buckholtz, Gavin A.
Gawalt, Ellen S.
author_facet Buckholtz, Gavin A.
Gawalt, Ellen S.
author_sort Buckholtz, Gavin A.
collection PubMed
description The formation of methyl-terminated carboxylic acid self-assembled monolayers (SAMs) with even numbers of carbons, from eighteen to thirty, was investigated on the oxide surface of Ti-6Al-4V and component metal oxides. Modified surfaces were characterized using diffuse reflectance infrared Fourier transform spectroscopy (DRIFT), matrix assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS) and contact angle analysis. Infrared spectroscopy indicated that using aerosol spray deposition techniques, stable, all-trans SAMs of octacosanoic (28 carbons) and triacontanoic (30 carbons) acids were formed on the alloy. Films were similarly formed on titanium and aluminum oxide. The surface of vanadium oxide exhibited limited reactivity. MALDI-TOF MS confirmed that formed films were monolayers, without multilayers or aggregates present. Water contact angles are indicative of the presence of hydrophobic methyl groups at the interface. This stable carboxylic acid SAM formation could be a useful alternative to phosphonic acid SAMs for corrosion and other applications.
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spelling pubmed-54488982017-07-28 Effect of Alkyl Chain Length on Carboxylic Acid SAMs on Ti-6Al-4V Buckholtz, Gavin A. Gawalt, Ellen S. Materials (Basel) Article The formation of methyl-terminated carboxylic acid self-assembled monolayers (SAMs) with even numbers of carbons, from eighteen to thirty, was investigated on the oxide surface of Ti-6Al-4V and component metal oxides. Modified surfaces were characterized using diffuse reflectance infrared Fourier transform spectroscopy (DRIFT), matrix assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS) and contact angle analysis. Infrared spectroscopy indicated that using aerosol spray deposition techniques, stable, all-trans SAMs of octacosanoic (28 carbons) and triacontanoic (30 carbons) acids were formed on the alloy. Films were similarly formed on titanium and aluminum oxide. The surface of vanadium oxide exhibited limited reactivity. MALDI-TOF MS confirmed that formed films were monolayers, without multilayers or aggregates present. Water contact angles are indicative of the presence of hydrophobic methyl groups at the interface. This stable carboxylic acid SAM formation could be a useful alternative to phosphonic acid SAMs for corrosion and other applications. MDPI 2012-07-09 /pmc/articles/PMC5448898/ http://dx.doi.org/10.3390/ma5071206 Text en © 2012 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Buckholtz, Gavin A.
Gawalt, Ellen S.
Effect of Alkyl Chain Length on Carboxylic Acid SAMs on Ti-6Al-4V
title Effect of Alkyl Chain Length on Carboxylic Acid SAMs on Ti-6Al-4V
title_full Effect of Alkyl Chain Length on Carboxylic Acid SAMs on Ti-6Al-4V
title_fullStr Effect of Alkyl Chain Length on Carboxylic Acid SAMs on Ti-6Al-4V
title_full_unstemmed Effect of Alkyl Chain Length on Carboxylic Acid SAMs on Ti-6Al-4V
title_short Effect of Alkyl Chain Length on Carboxylic Acid SAMs on Ti-6Al-4V
title_sort effect of alkyl chain length on carboxylic acid sams on ti-6al-4v
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5448898/
http://dx.doi.org/10.3390/ma5071206
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