Comparative study of equilibrium characteristics of Cu|Cu(II), Cu(I), glycine system containing sulfate or perchlorate as a supporting electrolyte

IF 0.5 4区 化学 Q4 CHEMISTRY, MULTIDISCIPLINARY Chemija Pub Date : 2019-12-04 DOI:10.6001/chemija.v30i4.4098
Kazimieras Mikulskis, S. Kanapeckaitė, A. Survila
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引用次数: 3

Abstract

2 Center for Physical Sciences and Technology, 3 Saulėtekio Avenue, 10222 Vilnius, Lithuania The distribution of species in Cu(II)-glycine solutions, containing sulfate or perchlorate as a supporting electrolyte, is considered. Substantial differences are observed at pH < 4.5, where the molar fraction of monoligand complex (associate) CuSO4 reaches up to 20 percent of the total Cu(II) concentration. Cu(I)-containing species are generated at the Cu|solution interface. These are Cu+ aqua-complexes (acid media) or monoand bidentate Cu(I)-glycine complexes (alkaline media). The addition of sulfate reduces the content of Cu+ ions, but practically does not affect the distribution of Cu(I) complexes. The study of acidbase equilibria involving Cu+ ions shows that the thermodynamic probability of Cu2O formation remains low in both perchlorate and sulfate media. HSO4 – ions formed in acid media should be treated as rather labile proton donors. This is quantitatively confirmed by experimental data, according to which the rate of hydrogen evolution increases correspondingly when perchlorate is replaced by sulfate in glycine solutions.
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含硫酸盐和高氯酸盐的Cu|Cu(II)、Cu(I)、甘氨酸体系平衡特性的比较研究
2物理科学与技术中心,3 Saulïtekio Avenue,10222维尔纽斯,立陶宛考虑了Cu(II)-甘氨酸溶液中的物种分布,该溶液含有硫酸盐或高氯酸盐作为支持电解质。在pH<4.5时观察到显著差异,其中单配体络合物(缔合)CuSO4的摩尔分数达到总Cu(II)浓度的20%。含Cu(I)的物种在Cu|溶液界面产生。这些是Cu+水络合物(酸性介质)或单齿和双齿Cu(I)-甘氨酸络合物(碱性介质)。硫酸盐的加入降低了Cu+离子的含量,但实际上并不影响Cu(I)配合物的分布。对Cu+离子酸碱平衡的研究表明,在高氯酸盐和硫酸盐介质中,Cu2O形成的热力学概率都很低。在酸性介质中形成的HSO4离子应被视为相当不稳定的质子供体。实验数据定量地证实了这一点,根据实验数据,当甘氨酸溶液中的高氯酸盐被硫酸盐取代时,析氢速率相应增加。
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来源期刊
Chemija
Chemija 化学-化学综合
CiteScore
1.30
自引率
16.70%
发文量
14
审稿时长
>12 weeks
期刊介绍: Chemija publishes original research articles and reviews from all branches of modern chemistry, including physical, inorganic, analytical, organic, polymer chemistry, electrochemistry, and multidisciplinary approaches.
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