油化学
Online ISSN : 1884-2003
ISSN-L : 0513-398X
プロパンスルトン誘導体の合成とその界面化学的性質について (第3報)
脂肪族アルコールおよび脂肪酸誘導体
平井 久夫石川 洋三須賀 恭一渡辺 昭次
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1967 年 16 巻 2 号 p. 75-80

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Surfactants (RiOC3H6SO3Na, RiCOOC3H6SO3Na) having propane sulfonate group were prepared from fatty alcohols (C10C18) and fatty acids (C10C18).
Surface active properties of their aqueous solutions were examined on surface tension, foaming power, foam stability and CMC at 50°C.
In comparison with sodium alkylsulfates (RiOSO3Na), the propane sultone derivatives exhibited lower Krafft point and cloud point, excellent surface tension and foaming power even at lower concentrations. The foam stability of these derivatives was similar to each other, but that of fatty acid derivatives was slightly inferior to the others.
The CMC values of the propane sultone derivatives were lower than those of sodium alkylsulfates, and relationship between the CMC and the number (N) of carbon atoms in the alkyl chain (Ri) was expressed as follows.
RiOC3H6SO3Na ; log CMC =1.15 - 0.292 N
RiCOOC3H6SO3Na ; log CMC = 0.99 - 0.296 N
RiOSO3Na ; log CMC =1.39 - 0.292 N
Furthermore, the relationship between the log CMC and the length of surface active ion (L, Å) could be represented as the following equations.
RiOC3H6SO3- ; log CMC = 3.09 - 0.233 L
RiCOOC3H6SO3- ; log CMC = 3.17 - 0.233 L
RiOSO3-; log CMC = 2.37 = 0.231 L
From these equations it is suggested that the hydrophilic groups of -O- and -COO- decrease the lipophilic property of the hydrocarbon chain by 1.4 and 0.7 units of -CH2- respectively in regard to the CMC value.

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