首页> 外文期刊>Tenside Surfactants Detergents: Journal for Theory, Technology and Application of Surfactants >Synthesis of New Family of Dialkylaryl Disulfonate Gemini Anionic Surfactant
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Synthesis of New Family of Dialkylaryl Disulfonate Gemini Anionic Surfactant

机译:新家族的二磺酸二烷基芳基酯双子阴离子表面活性剂的合成

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摘要

A new family of dialkylaryl disulfonate Gemini-type anionic surfactant were synthesized based on the reaction of olefin sulfonic acid(C_(14)AOS acid)with different aromatics.New synthesis route do not require the conventional alkylation unit and strong acid catalysts,and the resulting Gemini-type anionic surfactant differ from existing products by having the sulfonyl group attached to the alkyl chain rather than the aromatic ring.To optimizing reaction condition,a reliable double-wavelength spectrophoto-metric method and iodine value method were employed for measurement the conversion of the aromatics.The experimental has confirmed that the reaction time and temperature are mainly the factors of the effect of conversion.Under 150 deg C,C_(14)AOS acid reacts with different aromatics for 4 or 5 hours to form dialkyaryl disulfonic acid,and dialkyaryl disulfonic acid was then neutralized to dialkyaryl disulfonate Gemini-type anionic surfactant.Some surface active property has been investigated too.The critical micelle concentration of ditetrade-cylbenzene disulfonate,ditetradecylnaphthalene disulfonate,ditetradecylmethylnaphthalene disulfonate,ditetradecylphenan-threne disulfonate,ditetradecyldiphenylether sulfonate,ditetra-decyldiphenylmethane sulfonate and ditetradecylbenzophe-none sulfonate were 1.7x10~(-4),8.082 x10~(-6),2x10~(-5),2.158x10~(-3),5.0x10~(-6),1.0x10~(-5)and 1.33 x 10~(-5)mol l~(-1).Above datum showed the aromatics of the surfactant may effect on surface active property obviously.Among these,some dialkylaryl disulfonate gemini anionic surfactant have very higher surface active than conventional dodecylbenzene sulfonate and may be widely used in industry and household.
机译:基于烯烃磺酸(C_(14)AOS酸)与不同芳烃的反应,合成了一个新的二烷基芳基二磺酸盐双子座型阴离子表面活性剂。新的合成路线不需要常规的烷基化单元和强酸催化剂,得到的Gemini型阴离子表面活性剂与现有产品的不同之处在于其磺酰基连接在烷基链上而不是芳环上。为优化反应条件,采用可靠的双波长分光光度法和碘值法测量了转化率。实验证实反应时间和温度是影响转化率的主要因素。在150℃下,C_(14)AOS酸与不同的芳烃反应4或5小时,形成二芳基二磺酸,然后将二烷基芳基二磺酸中和为二烷基芳基二磺酸盐双子型阴离子表面活性剂。二十四烷基苯二磺酸盐,二十四烷基萘二磺酸盐,二十四烷基甲基萘二磺酸盐,二十四烷基菲蒽-二磺酸二磺酸盐,二十四烷基二苯醚磺酸盐,二十四烷基二苯甲烷磺酸盐和二十四烷基苯甲酸-四(十)磺酸盐(10,8)的临界胶束浓度分别为10〜(10)〜(8)10〜(10)〜(8)10〜(10) 6),2x10〜(-5),2.158x10〜(-3),5.0x10〜(-6),1.0x10〜(-5)和1.33 x 10〜(-5)mol l〜(-1)。从以上数据可以看出,表面活性剂的芳烃对表面活性的影响明显。其中,一些二烷基芳基二磺酸盐双基阴离子表面活性剂的表面活性比常规十二烷基苯磺酸盐高得多,可广泛用于工业和家庭。

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