U. Retter et al., EFFECT OF CHEMICAL-STRUCTURE ON HYDROLYSIS OF SILOXANE ALKYL AMMONIUMBROMIDES, Journal of colloid and interface science, 202(2), 1998, pp. 269-277
The influence of the chemical structure of siloxane alkyl ammonium bro
mides on their long-term stability in aqueous solution has been invest
igated by means of the change of the double layer capacity at the merc
ury/electrolyte interface and by mass spectroscopic measurements. Gene
rally, the degradation of the surfactants is caused by a hydrolytic cl
eavage of the siloxane bonds, leading to a loss of surface activity. S
uch a loss could be detected only in concentrated solutions (10(-1) M)
, not in those less than or equal to 10(-4) M. In the case of branched
trisiloxanes, the successive addition of a few methylene groups to on
e alkyl chain at the nitrogen atom resulted in a dramatic decrease of
the rate of hydrolysis. This effect is consistent with the assumption
that polar groups, located at the surface of siloxane micelles, protec
t the siloxane bonds against hydrolytic attack and that this protectio
n increases significantly with increasing alkyl chain length. (C) 1998
Academic Press.