Malmö University Publications
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Adsorption of delmopinol at the solid/liquid interface - the role of the acid-base equilibrium
Malmö högskola, Faculty of Health and Society (HS), Department of Biomedical Science (BMV).
Malmö högskola, Faculty of Health and Society (HS), Department of Biomedical Science (BMV).ORCID iD: 0009-0004-9546-0620
Sinclair Pharma AB, Ekonomivägen 5, SE-436 33 Askim, Sweden.ORCID iD: 0000-0003-2645-4636
Malmö högskola, Faculty of Health and Society (HS), Department of Biomedical Science (BMV).
2010 (English)In: Journal of Colloid and Interface Science, ISSN 0021-9797, E-ISSN 1095-7103, Vol. 350, no 1, p. 275-281Article in journal (Refereed) Published
Abstract [en]

Delmopinol is a tertiary amine surfactant that is used to counteract dental plaque formation. As it is of interest to understand the interfacial behavior from both fundamental and applied perspectives the adsorption of delmopinol to model surfaces was investigated. Adsorption on Teflon, titanium and stainless steel was studied by radioactive labeling and adsorption on silica was studied by quartz crystal microbalance (QCM), ellipsometry and particle electrophoresis. It was shown that the adsorption of delmopinol was complex and strongly influenced by pH and concentration. Pronounced peak values were detected in the adsorption curves (adsorbed amount versus concentration) exceeding the expected value for a bilayer type of structure. To account for this behavior two surface active component were assumed to be present. Accordingly, the high amounts result from the deposition of the component with lower solubility and the decrease at the critical micelle concentration can be explained by solubilization of this component. Based on data from several experimental methods and the pH dependence of the effect we propose an explanation in which the protonated and non-protonated forms of delmopinol represent the two components. However, it cannot be excluded that the component with the lower solubility could be a compound chemically different from delmopinol in the sample.

Place, publisher, year, edition, pages
Elsevier , 2010. Vol. 350, no 1, p. 275-281
Keywords [en]
surfactant adsorption
National Category
Physical Chemistry
Identifiers
URN: urn:nbn:se:mau:diva-5143DOI: 10.1016/j.jcis.2010.06.017ISI: 000281048300039PubMedID: 20619845Scopus ID: 2-s2.0-77955312365Local ID: 10678OAI: oai:DiVA.org:mau-5143DiVA, id: diva2:1401997
Available from: 2020-02-28 Created: 2020-02-28 Last updated: 2025-09-09Bibliographically approved

Open Access in DiVA

No full text in DiVA

Other links

Publisher's full textPubMedScopus

Authority records

Svensson, OlofHalthur, TobiasSjödin, TorgnyArnebrant, Thomas

Search in DiVA

By author/editor
Svensson, OlofHalthur, TobiasSjödin, TorgnyArnebrant, Thomas
By organisation
Department of Biomedical Science (BMV)
In the same journal
Journal of Colloid and Interface Science
Physical Chemistry

Search outside of DiVA

GoogleGoogle Scholar

doi
pubmed
urn-nbn

Altmetric score

doi
pubmed
urn-nbn
Total: 65 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf