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Long chain alkanesulfonates and 1‐hydroxy‐2‐alkanesulfonates: Structure and property relations
Author(s) -
Weil J. K.,
Smith F. D.,
Stirton A. J.,
Bistline R. G.
Publication year - 1963
Publication title -
journal of the american oil chemists' society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.512
H-Index - 117
eISSN - 1558-9331
pISSN - 0003-021X
DOI - 10.1007/bf02822460
Subject(s) - krafft temperature , chemistry , sodium , carbon chain , carbon fibers , critical micelle concentration , carbon atom , micelle , organic chemistry , amino acid , medicinal chemistry , inorganic chemistry , alkyl , biochemistry , aqueous solution , materials science , composite number , composite material
Even chain sodium alkanesulfonates from the Strecker reaction, odd chain sodium alkanesulfonates from the alkaline decarboxylation of ॅ‐sulfo acids, and sodium 1‐hydroxy‐2‐alkanesulfonates from the reduction of esters of ॅ‐sulfo acids were compared with respect to Krafft point, critical micelle concentration, detergency and foam height. Sodium alkanesulfonates and crude fusion products from the ॅ‐sulfo acids (mixtures of alkanesulfonates of one less carbon atom with a lesser amount of a soap of two less carbon atoms) are more soluble and have better detergent and foaming properties. Sodium 1‐hydroxy‐2‐alkanesulfonates resemble monosodium salts of ॅ‐sulfo acids. Alkanesulfonic acids and 1‐hydroxy‐2‐alkane‐sulfonic acids obtained from the sodium salts by ion exchange have lower Krafft points and are more readily soluble. The critical micelle concentrations of 1‐hydroxy‐2‐alkanesulfonic acids and ॅ‐sulfo acids are nearly the same and about equal to those of alkanesulfonic acids of one less carbon atom.