首页> 外文期刊>Indian Journal of Chemistry, Section A. Inorganic, Physical, Theoretical & Analytical >Micellar effect on the reacation of chromium(VI) oxidation of formaldehyde in the presence and absence of picolinic acid in aqueous acid media: A kinetic study
【24h】

Micellar effect on the reacation of chromium(VI) oxidation of formaldehyde in the presence and absence of picolinic acid in aqueous acid media: A kinetic study

机译:在存在和不存在吡啶甲酸的酸性介质中,胶束对甲醛铬(VI)氧化反应的动力学研究:动力学研究

获取原文
获取原文并翻译 | 示例
           

摘要

The kinetics and mechanism of Cr(VI) oxidation of formaldehyde in the presence and absence of picolinic acid (PA) in aqueous acid media have been carried out under the conditions, [formaldehydeh ? [Cr(VI)]T at different temperatures. Un- der the kinetic conditions, the monomeric species of Cr(VI) has been found kinetically active in the absence of PA while in the PA catalysed path, Cr(VI)-PA complex has been suggested as the active oxidant. In the PAcatalysed path, Cr(VI)-PA complex receives a nucleophilic attack by the substrate to form a ternary complex which subsequently experiences a redox decomposition (through 2e transfer) leading to formic acid and Cr(IV)-PA complex. Then Cr(IV)-PA complex participates further in the oxidation of formaldehyde and ultimately is converted into Cr(I11)-PA complex. In the uncatalysed path, Cr(VI)-substrate ester experiences an acid catalysed redox decomposition (2e transfer) at the rate determining step. The un- catalysed path shows a second order dependence on [H+] while the PA catalysed path shows a zeroth order dependence on [H+]. Both the uncatalysed and PA catalysed paths show first-order dependence on [formaldehyde]T and [Cr(VI)]T. The PA catalysed path is first order in [PA]T. All these observations (i.e. dependence patterns on the reactants) remain unaltered in the presence of externally added surfactants. Effect of cationic surfactant (i.e. cetylpyridinium chloride, CPC) and anionic surfactant (i.e. sodium dodecyl sulphate, SDS) has been studied both in the presence and absence of PA. CPC inhibits the reactions while SDS catalyses the reactions. The observed micellar effects have been explained by considering the parti- tioning of the reactants between the micellar and aqueous phase. Applicability of different kinetic models, e.g. pseudo-phase ion exchange (PIE) model, Menger-Portnoy model, Piszkiewicz cooperative model, has been tested to explain the observed micellar effects.
机译:在酸性条件下,在存在和不存在吡啶甲酸(PA)的条件下,进行了Cr(VI)氧化甲醛的动力学和机理。 [Cr(VI)] T在不同温度下。在动力学条件下,已发现在不存在PA的情况下Cr(VI)的单体具有动力学活性,而在PA催化的路径中,已表明Cr(VI)-PA络合物可作为活性氧化剂。在PA催化的路径中,Cr(VI)-PA配合物受到底物的亲核攻击,形成三元配合物,随后发生氧化还原分解(通过2e转移),形成甲酸和Cr(IV)-PA配合物。然后,Cr(IV)-PA络合物进一步参与甲醛的氧化,最终转化为Cr(I11)-PA络合物。在未催化的路径中,Cr(VI)-底物酯在速率确定步骤经历酸催化的氧化还原分解(2e转移)。未催化的路径显示对[H +]的二阶依赖性,而PA催化的路径显示对[H +]的零阶依赖性。未催化路径和PA催化路径均显示对[甲醛] T和[Cr(VI)] T的一级依赖性。 PA催化的路径是[PA] T中的一阶。在外部添加的表面活性剂的存在下,所有这些观察结果(即,对反应物的依赖性模式)保持不变。在存在和不存在PA的情况下,均已研究了阳离子表面活性剂(即十六烷基氯化吡啶鎓,CPC)和阴离子表面活性剂(即十二烷基硫酸钠,SDS)的作用。 CPC抑制反应,而SDS催化反应。考虑到胶束和水相之间的反应物分配,可以解释观察到的胶束效应。不同动力学模型的适用性,例如伪相离子交换(PIE)模型,Menger-Portnoy模型,Piszkiewicz合作模型已通过测试来解释观察到的胶束效应。

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