1996
DOI: 10.1007/bf00658374
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The aggregation ofn-dodecanephosphonic acid in water

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Cited by 11 publications
(13 citation statements)
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“…This would produce a drop in the apparent acidity constant (K a1 ) and an increase of pK a1 when the size of the aggregates grows. This has already been observed in aqueous n-dodecanephosphonic acid systems, 12 where the pK a1 varies from 4.03 in non-micellized molecules to about 6 in micelles and 6.74 in lamellar mesophases. Moreover, the approaching between polar head groups produces an increase in the Stern layer surface potential, which in turn causes a reduction in the micelle ionization degree.…”
Section: ■ Experimental Sectionsupporting
confidence: 63%
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“…This would produce a drop in the apparent acidity constant (K a1 ) and an increase of pK a1 when the size of the aggregates grows. This has already been observed in aqueous n-dodecanephosphonic acid systems, 12 where the pK a1 varies from 4.03 in non-micellized molecules to about 6 in micelles and 6.74 in lamellar mesophases. Moreover, the approaching between polar head groups produces an increase in the Stern layer surface potential, which in turn causes a reduction in the micelle ionization degree.…”
Section: ■ Experimental Sectionsupporting
confidence: 63%
“…This was verified using ion-selective electrodes in micelles of dodecanephosphonic acid. 12 The reduction in [H 3 O + ] at higher DPA concentration is caused by the formation of a lamellar mesophase with lower ionization. The reason for the subsequent decrease is that, when the aggregates grow to form multilamellar vesicles or an emulsified lamellar mesophase, much of the added surfactant is enclosed inside the aggregates and cannot contribute to the formation of hydrogen ions.…”
Section: ■ Experimental Sectionmentioning
confidence: 99%
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“…The same behaviour was observed in sodium dehydrocholate micelar solutions [12]. However, in some anionic surfactants, such as SDS [9] sodium perfluorooctanoate [13], and n-alkane phosphonic acids [14,15] [16].…”
Section: Polarographic and Voltammetric Methods Applied To Surfactantsupporting
confidence: 65%
“…Moreover, zwitterionic surfactants have lower critical micelle concentration (CMC) than anionic, cationic or nonionic ones. For example, the CMCs of CTAB, DBSA, and N-Dodecylphosphonic acid, determined in water at room temperature are 0.90, 0.55, and 0.54 mM/L, respectively. The CMC of sulfobetaine surfactant SB3C16 is 0.02 mM/L . It is very important parameter, because nanoparticles are formed at a concentration of surfactant above its critical value.…”
Section: Introductionmentioning
confidence: 99%