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Forces between two glass surfaces with adsorbed hexadecyltrimethylammonium salicylate
KTH, Tidigare Institutioner (före 2005), Kemi.ORCID-id: 0000-0002-8935-8070
2000 (Engelska)Ingår i: Langmuir, ISSN 0743-7463, E-ISSN 1520-5827, Vol. 16, nr 4, s. 1937-1942Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Forces have been measured for hexadecyltrimethylammonium salicylate (C(16)TASal) layers on glass beads. During the inward process, hydrophobic attraction occurred at lower adsorption of C(16)TASal and electrostatic repulsion interactions happened at higher adsorption. While the jump-in phenomenon was observed for solutions of concentrations below the critical micelle concentration (cmc = 0.15 mM), the step-in phenomenon was characteristic for solutions at the cme and above the cmc, suggesting the push-out of adsorbed C(16)TASal layers and/or inserted micelles. The remarkable pull-off phenomenon on the outward process occurred for all solutions, indicating a strong interaction between C(16)TASal molecules. For aqueous 0.15 mM C(16)TASal solutions of various NaSal concentrations, on the inward process, the electrostatic repulsive interaction decreased with adding NaSal. This is due to the electrostatic shielding by salt excess. The height of the force wall on the inward process reached a maximum at 0.01 M NaSal, but the interlocking between molecules on two surfaces during the outward process was minimized at 0.1 M NaSal. These tendencies, which are different from that of the electrostatic repulsion interaction, imply the strong cohesion between adsorbed C(16)TASal layers.

Ort, förlag, år, upplaga, sidor
2000. Vol. 16, nr 4, s. 1937-1942
Nyckelord [en]
surfactant, salicylate, micelle, adsorption, surface force
Nationell ämneskategori
Naturvetenskap
Identifikatorer
URN: urn:nbn:se:kth:diva-48324DOI: 10.1021/la990824yISI: 000085412600065PubMedID: 19231831Scopus ID: 2-s2.0-0033906706OAI: oai:DiVA.org:kth-48324DiVA, id: diva2:459472
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QC 20111130Tillgänglig från: 2011-11-25 Skapad: 2011-11-17 Senast uppdaterad: 2022-06-24Bibliografiskt granskad

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