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ADSORPTION OF THIOUREA AND ITS METHYL DERIVATIVES FROM CHLORATE(VII) WITH VARIED WATER ACTIVITY

机译:可变水活度从氯酸盐(VII)中吸附硫脲及其甲基衍生物

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The comparison of thiourea, methylthiourea, dimethylthiourea and tetramethylthiourea adsorption at mercury|sodium chlorate(VII) interface was done. For the sake of due to the specific interactions between sulfur and mercury all the compounds examined are pointed with their negative end towards mercury, even at the negative values of an electrode charge. However the change of an electrode charge is connected with the change of an adsorbate reorientation. It was found that with the increase of the methyl group amount in a molecule of thiourea methyl derivatives: (i) the range of adsorption potentials is expanded, (ii) the values of zero charge potentials and surface tension decrease, (iii) the surface excesses increase. Whereas the considerable changes of adsorption energy values were not fund. The lack of symmetry results in a molecule, while the methylthiourea interaction constants are much more higher than the interaction constants of the other compounds examined. The changes of adsorption parameters as a function of the supporting electrolyte concentration are analogous for all the adsorbates examined. They point to the competitive adsorption of thiourea methyl derivatives and ClO^sub 4^^sup -^. [PUBLICATION ABSTRACT]
机译:比较了硫脲,甲基硫脲,二甲基硫脲和四甲基硫脲在氯酸钠(VII)界面上的吸附。由于硫和汞之间的特定相互作用,因此所检查的所有化合物的负极均指向汞,即使电极电荷为负值也是如此。然而,电极电荷的变化与被吸附物重取向的变化有关。发现随着硫脲甲基衍生物分子中甲基量的增加:(i)吸附电位的范围扩大,(ii)零电荷电位的值和表面张力降低,(iii)表面过度增加。然而,吸附能值的显着变化是没有资金的。缺乏对称性导致产生分子,而甲硫脲的相互作用常数比其他所研究化合物的相互作用常数高得多。对于所检查的所有被吸附物,作为支持电解质浓度的函数的吸附参数的变化是相似的。他们指出了硫脲甲基衍生物和ClO 2亚砜的竞争吸附。 [出版物摘要]

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    Agnieszka NOSAL-WIERCINSKA1,* and Mariusz GROCHOWSKI2Faculty of Chemistry, Maria Curie-Sklodowska Univeristy, 20-031 Lublin, Poland, e-mail: 1 anosal@poczta.umcs.lublin.pl, 2 mariusz.grochowski@poczta.umcs.lublin.plReceived October 13, 2010Accepted February 7, 2011Published online March 15, 2011,;

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