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Preparation and properties of sulfonate salt‐type cleavable surfactants with a 1,3‐dioxane ring
Author(s) -
Wang GuanWu,
Yuan XianYou,
Liu YouCheng,
Lei XueGong
Publication year - 1994
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/bf02541429
Subject(s) - chemistry , pulmonary surfactant , sulfonate , hydrolysis , alkyl , sodium hydride , hydroxymethyl , critical micelle concentration , salt (chemistry) , micelle , condensation , polymer chemistry , condensation reaction , organic chemistry , sodium , catalysis , aqueous solution , biochemistry , physics , thermodynamics
Abstract A series of di‐anionic cleavable surfactants were prepared by the condensation of aldehydes with 2,2‐ bis (hydroxymethyl)‐1,3‐propanediol, followed by reaction with 1,3‐propanesultone in the presence of sodium hydride. Surfactant 5a had a different 1 H nuclear magnetic resonance spectrum in D 2 O than products 5b−d. This was rationalized by its different conformation, which originates from the self‐coiling of its alkyl chain. The critical micelle concentrations, Krafft points and hydrolysis properties of these surfactants were determined.

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