2001
DOI: 10.1006/jcis.2001.7836
|View full text |Cite
|
Sign up to set email alerts
|

Self-Assembly in the System Decanoic Acid–Butylamine–Water

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

0
15
0

Year Published

2005
2005
2017
2017

Publication Types

Select...
6

Relationship

0
6

Authors

Journals

citations
Cited by 17 publications
(15 citation statements)
references
References 55 publications
(43 reference statements)
0
15
0
Order By: Relevance
“…Contrary to this, above the CMC the viscosity increases exponentially with increasing concentration for the methacrylate counterion, while it increases only slightly for the acrylate counterion. Such a sharp increase is usually attributed to a micellar growth with a transition from discrete spherical aggregates to larger elongated micelles [22,34,36,82,83]. According to this, in the present case it is shown that the presence of the methacrylate counterion leads to a different shape of the aggregates, indicating that there is a trend to form elongated micelles, whereas with an acrylate counterion the surfactant (da + a − ) forms spherical micelles.…”
Section: Isotropic L1 Phasementioning
confidence: 55%
See 1 more Smart Citation
“…Contrary to this, above the CMC the viscosity increases exponentially with increasing concentration for the methacrylate counterion, while it increases only slightly for the acrylate counterion. Such a sharp increase is usually attributed to a micellar growth with a transition from discrete spherical aggregates to larger elongated micelles [22,34,36,82,83]. According to this, in the present case it is shown that the presence of the methacrylate counterion leads to a different shape of the aggregates, indicating that there is a trend to form elongated micelles, whereas with an acrylate counterion the surfactant (da + a − ) forms spherical micelles.…”
Section: Isotropic L1 Phasementioning
confidence: 55%
“…Depending on the lengths of the alkyl chains, the resulting salts are considered as catanionic surfactants [22][23][24][25][26][27][28][29][30][31][32][33] or surfactants with an organic counterion [3,[34][35][36]. Backlund and co-workers [24,34] investigated the ternary phase behavior of the acetic acid/dodecylamine/water system and found an isotropic region (micelles), a cubic phase, and both lamellar and hexagonal lyotropic liquid crystalline (LLC) phases.…”
Section: Introductionmentioning
confidence: 99%
“…The conclusion relevant to our discussion borne out from these experimental results is that, depending on the water content, a fraction of the short moiety of a catanionic surfactant (i.e. the organic counterion) is aggregated in the micelle (or lyotropic liquid crystal), while the remaining fraction resides free (unbound) [49].…”
Section: Overview On the Molecular Desorption Of Catanionic Surfactantsmentioning
confidence: 92%
“…For the paired surfactants formed by alkyl ammonium and alkyl carboxylate, when the chains contain equal numbers of carbon atom and are long enough, the phase behavior is typical of a "true" ion-pair amphiphile or catanionic surfactant [11]. However, if the carbon atom number is sufficiently unbalanced between the cationic and anionic chains, the phase behavior resembles more that of a surfactant with an organic counterion [43][44][45][46][47][48][49]. The conclusion relevant to our discussion borne out from these experimental results is that, depending on the water content, a fraction of the short moiety of a catanionic surfactant (i.e.…”
Section: Overview On the Molecular Desorption Of Catanionic Surfactantsmentioning
confidence: 92%
“…Above the critical micelle concentration (CMC), surfactants aggregate in micelles, and at higher concentrations they can form lyotropic liquid crystal (LLC) phases [4,[12][13][14][15][16][17][18][19][20][21]. The type of LLC phases (e.g., lamellar, cubic, or hexagonal) can be deduced from the texture observed by polarized optical microscopy (POM).…”
Section: Introductionmentioning
confidence: 99%