In:
Journal of the American Oil Chemists' Society, Wiley, Vol. 71, No. 7 ( 1994-07), p. 727-730
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.
Type of Medium:
Online Resource
ISSN:
0003-021X
,
1558-9331
Language:
English
Publisher:
Wiley
Publication Date:
1994
detail.hit.zdb_id:
2041388-9
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