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氨基磺酸系两性表面活性剂的新合成法及其机理推断

Novel synthesizing method and mechanism deducing for sulfamic acid series amphoteric surfactant

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【作者】 汤芝平薛永强赵红

【Author】 Tang Zhiping Xue Yongqiang Zhao Hong (College of Chemistry and Chemical Engineering,Taiyuan University of Technology,Taiyuan 030024,China)

【机构】 太原理工大学化学化工学院太原理工大学化学化工学院 山西太原030024山西太原030024

【摘要】 给出了一种以烷基胺、HCHO与无机磺化剂(NaHSO3或Na2SO3)为原料,经由胺羟甲基化、磺化与固相成盐三步反应,合成氨基磺酸系两性表面活性剂的新合成法。同时,基于曼尼奇反应、磺甲基化和N-烷基化等反应的历程,推断了新合成法的反应机理。结果表明,新合成法的收率高(86.7%);反应主要为亲核加成历程;胺羟甲基化反应pH值高,有利于H+的脱离,促进反应正向移动和中间体的稳定;磺化反应体系酸性越强,越有利于中间体上OH的离去,加速反应正向移动;固相成盐反应简单可行;机理推断结果符合实验和相关文献报道的结果。

【Abstract】 A novel method for synthesizing sulfamic acid series amphoteric surfaetant,that uses the materials of alkyl a- mine,HCHO and abio-sulfonation agent (NaHSO3 or Na2SO3)with three steps:amine hydroxymethylation,sulfonation and solid state reaction,has been put forward.Meanwhile,based on the mechanism of Mannich reaction,sulfomethylation reaction and N-alkylation raction etc,the mechanism of this novel method has been deduced.The results show that the novel method has high yield of 86.7%;the mechanism of this method is main about nucleophilic addition reaction;in the amine hydroxymeth- ylation,the higher pH value,the better H+ being away,which promotes this reaction positive shifting and the intermediate’s stability;in the sulfonation,strong acid is in favor of OH deviating,which accelerates the reaction positive shifting,too;the solid state reaction is available and easy;and the mechanism deducing results are identical to the experiment results and relative literature reports.

  • 【文献出处】 化学工业与工程技术 ,Journal of Chemical Industry & Engineering , 编辑部邮箱 ,2008年01期
  • 【分类号】TQ423
  • 【被引频次】8
  • 【下载频次】369
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