2016
DOI: 10.1007/s11743-016-1795-x
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Surface Parameters and Biological Activity of N‐(3‐(Dimethyl Benzyl Ammonio) Propyl) Alkanamide Chloride Cationic Surfactants

Abstract: Three cationic surfactants containing amide groups were prepared by quaternization of dimethylaminopropylamine with benzyl chloride. FTIR and 1 H-NMR spectroscopy were used to confirm the chemical structure of the prepared cationic surfactants. The surface parameters were estimated using surface tension measurements at three different temperatures. The prepared cationic surfactant showed a lower CMC than conventional cationic surfactants. Thermodynamic parameters of adsorption and micellization depend mainly o… Show more

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Cited by 38 publications
(14 citation statements)
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References 48 publications
(55 reference statements)
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“…Similar results can be found in literatures, such as the A S values of 1.05-1.43 nm 2 were obtained for quaternary ammonium salt hydrocarbon gemini surfactants (Alami et al, 1993;Yoshimura et al, 2006). The A S value of 1.75 nm 2 was measured for alkanamide chloride cationic surfactants (Shaban et al, 2016). The large A S values probably are related to the weak hydrophobic interactions of the ester group and strong electrostatic repulsion between neighboring cationic head groups of surfactant (Benbayer et al, 2013;Shen et al, 2018).…”
Section: Surface Activity Of Sfhcs Solutionssupporting
confidence: 89%
“…Similar results can be found in literatures, such as the A S values of 1.05-1.43 nm 2 were obtained for quaternary ammonium salt hydrocarbon gemini surfactants (Alami et al, 1993;Yoshimura et al, 2006). The A S value of 1.75 nm 2 was measured for alkanamide chloride cationic surfactants (Shaban et al, 2016). The large A S values probably are related to the weak hydrophobic interactions of the ester group and strong electrostatic repulsion between neighboring cationic head groups of surfactant (Benbayer et al, 2013;Shen et al, 2018).…”
Section: Surface Activity Of Sfhcs Solutionssupporting
confidence: 89%
“…π cmc decreased with increasing temperature and salinity. The maximum surface excess decreased with temperature and increased with salinity because of the decrease in the repulsion forces between the hydrophobic tail and the aqueous medium, which ultimately reduced the concentration of surfactant molecules at the air/water interface (Shaban, Aiad, & Ismail, ). However, the minimum surface area per molecule increased with the temperature and decreased by increasing the salinity.…”
Section: Resultsmentioning
confidence: 99%
“…By reduction in the г max values, the distance between the interface and surfactant monomers increase. High temperature reduces the repulsion between the hydrophobic tail and the aqueous medium, which favors the horizontal orientation of the molecule at the interface, hence increasing A min (Shaban et al, ). A slight decrease of the A min value in FW may be due to the increase in concentration of the divalent ions (Ca 2+ , Mg 2+ ), which favors the shielding of surfactant head charges (Demissie & Duraisamy, ).…”
Section: Resultsmentioning
confidence: 99%
“…The concentration of the surfactant is 10 mM. The procedures were described in previous work (Shaban et al, 2016a).…”
Section: Biological Activitymentioning
confidence: 99%