CHEMICAL-STRUCTURE AND SURFACE-ACTIVITY .30. SYNTHESIS AND SURFACE-PROPERTIES OF CHEMODEGRADABLE ANIONIC SURFACTANTS - SODIUM (2-N-ALKYL-1,3-DIOXAN-5-YL)SULFATES
A. Piasecki et al., CHEMICAL-STRUCTURE AND SURFACE-ACTIVITY .30. SYNTHESIS AND SURFACE-PROPERTIES OF CHEMODEGRADABLE ANIONIC SURFACTANTS - SODIUM (2-N-ALKYL-1,3-DIOXAN-5-YL)SULFATES, Journal of the American Oil Chemists' Society, 74(1), 1997, pp. 33-37
In the reaction of cis- and trans-2-n-alkyl-5- hydroxy-1,3-dioxane mix
tures with SO3 . pyridine complex, followed by neutralization with sod
ium hydroxide or sodium carbonate, a new group of anionic surfactants,
i.e., sodium cis- and trans-(2-n-alkyl-1,3-dioxan-5-yl)sulfate were o
btained. The hydrophobic intermediates used in the sulfation reaction
were obtained in high yields from four-component glycerol acetals by t
he process of transacetalization and selective crystallization of 1,3-
dioxane derivatives. The physical data of the new compounds and some o
f their surface properties, such as critical micelle concentration (CM
C), effectiveness of water surface tension reduction Gamma I-CMC, stan
dard free energies of adsorption and micellization, Delta G(ads)(0) an
d Delta G(CMC)(0), surface excess concentration, Gamma(CMC), and the s
urface area demand per molecule, A(CMC) were determined. It was shown
that the surface activity of the standard anionic surfactant sodium do
decyl sulfate should be similar to the surface activity of sodium (2-n
-decyl-1,3-dioxan 5-yl)sulfate.