首页> 外文期刊>Journal of Solution Chemistry >Hetero-aromatic Nitrogen Base Promoted Cr(VI) Oxidation of Butanal in Aqueous Micellar Medium at Room Temperature and Atmospheric Pressure
【24h】

Hetero-aromatic Nitrogen Base Promoted Cr(VI) Oxidation of Butanal in Aqueous Micellar Medium at Room Temperature and Atmospheric Pressure

机译:在室温和大气压下,杂芳族氮基促进了胶束水溶液中丁醛的Cr(VI)氧化。

获取原文
获取原文并翻译 | 示例
           

摘要

The kinetics of the oxidation of butanal by chromic acid in aqueous and aqueous surfactant (sodium dodecyl sulfate, SDS, Triton X-100 (TX-100) and N-cetylpyridinium chloride, CPC) media have been investigated in the presence of a promoter at 303 K. The pseudo-first-order rate constants (k (obs)) were determined from a logarithmic plot of absorbance as a function time. The rate constants were found to increase with introduction of heteroaromatic nitrogen base promoters such as picolinic acid (PA), 2, 2'-bipyridine (bipy) and 1,10-phenanthroline (phen). The product, butanoic acid, was characterized by H-1-NMR. Three promoters PA, bpy and phen are used in combination with SDS, TX-100 and CPC surfactants showing an increase in the rate of oxidation compared to the unpromoted pathway. The mechanism of the reaction path has been proposed with the help of kinetic results and spectroscopic studies. The observed net enhancement of rate effects has been explained by considering the hydrophobic and electrostatic interaction between the surfactants and reactants. The TX-100 and PA combination is suitable for butanal oxidation.
机译:在有促进剂存在的条件下,研究了在水性和水性表面活性剂(十二烷基硫酸钠,SDS,Triton X-100(TX-100)和N-十六烷基吡啶鎓氯化物,CPC)中铬酸氧化丁醛的动力学。 303 K.伪一阶速率常数(k(obs))由吸光度与功能时间的对数关系图确定。发现速率常数随引入杂芳族氮碱启动子如吡啶甲酸(PA),2,2'-联吡啶(bipy)和1,10-菲咯啉(phen)而增加。产物丁酸通过H-1-NMR表征。三种促进剂PA,bpy和phen与SDS,TX-100和CPC表面活性剂结合使用,与未促进途径相比,显示出氧化速率的提高。已经通过动力学结果和光谱学研究提出了反应路径的机理。通过考虑表面活性剂和反应物之间的疏水和静电相互作用,可以解释所观察到的速率效应的净增强。 TX-100和PA的组合适用于丁醛氧化。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号