journal article·1996-01-01

Preparing Nontoxic Microemulsions with Alkyl Monoglucosides and the Role of Alkanediols as Cosolvents

M. Kahlweit, G. Busse, B. Faulhaber

Langmuir· Volume 12· Issue 4
Publisher page

Abstract

Experiments tell that the emulsification of mineral oils by lecithins, or glucosides, requires the addition of alcohols as cosolvents. In our first studies we used alkanols for this purpose. However, for preparing nontoxic microemulsions with biological oils, the alkanols, too, must be substituted by nontoxic alcohols. In this paper we show that n -alkane-1,2-diols (C i -diols) are efficient substitutes, with medium-chain diols ( i ≤ 6) playing the role of propanol and the longer-chain C 8 -diol that of butanol. After having recently demonstrated how to prepare microemulsions with a long-chain lecithin and C 5 -diol, we show in this paper how to prepare nontoxic microemulsions with a long-chain monoglucoside and C 8 -diol.
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Research context

OpenAlex topics: Surfactants and Colloidal Systems · Carbohydrate Chemistry and Synthesis

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Max-Planck-Institut für Biophysikalische Chemie, Postfach 2841, D-37018 Göttingen, Germany

References (5)

Show source-provided references
1. Kahlweit M. · Langmuir · 1995 · 11 · 418510.1021/la00011a001 ↗
2. Shinoda K. · J. Dispersion Sci. Technol. · 1988 · 9 · 55510.1080/01932698808944010 ↗
3. Kahlweit M. · Langmuir · 1995 · 11 · 157610.1021/la00005a027 ↗
4. Kahlweit M. · Langmuir · 1995 · 11 · 338210.1021/la00009a019 ↗
5. Kahlweit M. · Langmuir · 1989 · 5 · 30510.1021/la00086a002 ↗