首页> 外文期刊>Russian Journal of General Chemistry >Adsorption on Quartz of Co(II), Ni(II), and Cu(II) in the Form of Hydroxide Nanoparticles or Metal Ionic Species from Solutions with pH Close to That of the Onset of Hydroxide Formation
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Adsorption on Quartz of Co(II), Ni(II), and Cu(II) in the Form of Hydroxide Nanoparticles or Metal Ionic Species from Solutions with pH Close to That of the Onset of Hydroxide Formation

机译:pH值接近氢氧化物生成开始时溶液中氢氧化物纳米颗粒或金属离子形式对Co(II),Ni(II)和Cu(II)的吸附

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摘要

The kinetics of adsorption and desorption of Co(II), Ni(II), and Cu(II) from aqueous solutions were studied at such pH values when the prevailing metal species in the continuous phase is either hydroxide of Me~(2+) (at pH only slightly lower than that at which the hydroxide starts to precipitate). The desorption was performed by methods producing different effects on the adsorbed layer. The time of the preceding adsorption was also varied. a significant different effects on the adsorbed layer. The time of the preceding adsorption was also varied. a significant difference in the adsorption-desorption behavior of the metals was revealed. This difference cannot be explained without considering the effects related to the detailed electronic structure of metal species and of the adsorbent active centers. The observed trends are attributed to the difference in the properties of the metals as electron pair acceptors and of the surface coordination compounds formed.
机译:当连续相中主要的金属种类是Me〜(2+)的氢氧化物时,在这样的pH值下研究了Co(II),Ni(II)和Cu(II)从水溶液中的吸附和解吸动力学。 (在pH值仅略低于氢氧化物开始沉淀的pH值)。通过对吸附层产生不同影响的方法进行解吸。先前的吸附时间也有所不同。对吸附层的影响明显不同。先前的吸附时间也有所不同。结果表明,金属的吸附-解吸行为存在显着差异。如果不考虑与金属种类和吸附活性中心的详细电子结构有关的影响,就无法解释这种差异。观察到的趋势归因于作为电子对受体的金属和所形成的表面配位化合物的性能差异。

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