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Gemini表面活性剂C_(12)-3-C_(12)·2Br及C_(12)-3(OH)-C_(12)·2Cl的合成及表面活性 被引量:6

Study on synthesis and surface activities of the Gemini surfactants C_(12)-3-C_(12)·2Br and C_(12)-3(OH)-C_(12)·2Cl
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摘要 合成了联结基团分别为亚甲基链及含羟基亚甲基链的两种季铵盐Gemini表面活性剂,即C12-3-C12.2Br及C12-3(OH)-C12.2Cl。用红外光谱、核磁共振及元素分析对它们的结构进行了鉴定,并对影响反应的因素进行了研究,得出了合成C12-3-C12.2Br的最佳条件为:n(N,N-二甲基十二烷基胺)∶n(1,3-二溴丙烷)=2.2∶1.0,以乙醇作溶剂,在回流温度下反应24 h,产率可达80%以上。合成C12-3(OH)-C12.2Cl的最佳条件为n(二甲基十二烷基叔胺)∶n(二甲基十二烷基叔胺盐酸盐)∶n(环氧氯丙烷)=2.0∶1.0∶1.0,以正丙醇为溶剂,在回流温度下反应3 h,产率可达94.5%以上。测定了它们的表面张力γ、临界胶束浓度cmc及降低水溶液表面张力的效率C20,结果表明:与相应的单头基单烷烃链表面活性剂相比,Gemini表面活性剂具有很低的cmc和很强的表面活性,联结基团对其性能有较大的影响。 Two kinds of quaternary-ammonium Gemini surfactants were synthesized,with their spacer chain comprising methylene radicals and methylene radicals with hydroxyl groups and their molecular formula equating to C12-3-C12·2Br and C12-3(OH)-C12·2Cl,respectively.Their structures were also confirmed by IR,^1HNNR and elemental analysis.Meanwhile the factors affecting the reaction were discussed.The optimum condition for synthesizing C12-3-C12·2Br was as follows:n(C12H25N(CH3)2)∶n(1,3-dibromopropane)=2.0∶1.0 using ethanol as the solvent,with the reaction carried out for 24 h in reflux,and the product yield was 80%.The optimum condition for synthesizing C12-3(OH)-C12·2Cl was as follows:n(C12H25N(CH3)2)∶n(C12H25N(CH3)2·HCl)∶n(chloroepoxy propane)=2.0∶1.0∶1.0,using n-propanol as the solvent,with the reaction carried out for 3 h in reflux,and the product yield was 94.5%.Furthermore,the surface tension(γ),the critical micelle concentration(cmc) and the efficiency for decreasing the surface tension(C20) were also measured.Test results showed that the Gemini surfactants had a much lower cmc and stronger surface activity compared with the corresponding conventional surfactants,and their surface activity was affected remarkably by spacer chain.
作者 叶志文
出处 《化学试剂》 CAS CSCD 北大核心 2007年第9期513-516,571,共5页 Chemical Reagents
关键词 GEMINI表面活性剂 合成 联结基团 羟基 表面活性 Gemini surfactant synthesis spacer chain hydroxyl surface activity
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参考文献6

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