从盐酸溶液中提取 (IV) 离子的液体-液体提取,使用在煤油中溶解的Aliquat 336
1Hot Laboratories Center, Egyptian Atomic Energy Authority, Cairo, 13759, Egypt.
BMC chemistry
|September 28, 2024
概括
这项研究表明,在煤油中使用Aliquat 336有效地用溶剂提取 (IV),从缩盐酸溶液中获得高回收率. 优化的方法显示出从工业液中回收的前景.
科学领域:
- 化学工程是化学工程的重要组成部分.
- 水电金术是指用水电金术进行金术.
- 分离科学 分离科学
背景情况:
- 的回收对环境保护和资源利用至关重要.
- 盐酸介质对选择性金属提取提出了挑战.
- 阿利卡特336是一种四级盐,以其在液体-液体提取中的潜力而闻名.
研究的目的:
- 通过使用Aliquat 336.6从缩的盐酸中提取 (IV) 的溶剂.
- 为了优化提取参数并阐明提取机制.
- 评估从工业溶液中回收的方法的可行性.
主要方法:
- 使用0.4mol/L Aliquat 336在煤油中与1-octanol作为修饰剂进行溶剂提取.
- 对参数进行系统研究:酸度,时间,金属离子度,负载能力,稀释剂和温度.
- 使用斜率分析和富里埃变换红外光谱 (FT-IR) 来识别提取的物种.
- 提取过程的热力学分析.
主要成果:
- 获得了的高提取效率 (IV),达到92%在8mol/L HCl和97.1%在1mol/L Aliquat 336.6.
- 最佳的有机阶段包括Aliquat 336在煤油中与1-octanol.
- 提取的物种被确定为[H2SeO2Cl2.2R4NCl]org,提取平衡常数 (Kex) 为 26.17 ± 2 M-2.
- 由于安全,经济和环境因素,煤油被确定为首选的稀释剂.
结论:
- 开发的溶剂提取方法对于从缩的HCl中恢复是非常有效的.
- 该过程是内热的,如热力学参数所示.
- 该方法显示了从阳极粘液浸出液中回收的实际应用潜力.
相关概念视频
Extraction: Advanced Methods
431
Metal ions can be separated from one another by complexation with organic ligands–the chelating agent– to form uncharged chelates. Here, the chelating agent must contain hydrophobic groups and behave as a weak acid, losing a proton to bind with the metal. Since most organic ligands used in this process are insoluble or undergo oxidation in the aqueous phase, the chelating agent is initially added to the organic phase and extracted into the aqueous phase. The metal-ligand complex is...
431
Precipitation of Ions
27.8K
Predicting Precipitation
The equation that describes the equilibrium between solid calcium carbonate and its solvated ions is:
The equation that describes the equilibrium between solid calcium carbonate and its solvated ions is:
27.8K
High-Performance Liquid Chromatography: Elution Process
435
In High-Performance Liquid Chromatography (HPLC), the elution process is critical to the separation of analytes and the quality of chromatographic results. Elution describes how compounds move through the column and separate based on their interactions with the mobile and stationary phases. This process determines the resolution, peak shape, and retention times in the chromatogram, which are essential for identifying and quantifying components in complex mixtures. Understanding the elution...
435
Washing, Drying, and Ignition of Precipitates
883
After filtration, the precipitate is washed to remove coprecipitated impurities and any remaining mother liquor. Colloidal precipitates, such as silver chloride, are washed with an electrolyte (such as dilute nitric acid) to prevent the peptization of the precipitate. In the case of slightly soluble precipitates, the wash solution contains a common ion to reduce solubility. Lead sulfate, which is slightly soluble in water, is washed with dilute sulfuric acid. Similarly, wash solutions may be...
883
Precipitation and Co-precipitation
1.7K
Precipitation and coprecipitation methods can be used to separate a mixture of ions in a solution. In qualitative inorganic analysis, ions that form sparingly soluble precipitates with the same reagent are separated based on the differences in solubility products. For example, consider the separation of Cu(II) and Fe(II) ions by precipitation as insoluble sulfides. First, copper(II) sulfide is precipitated by the addition of acidic H2S, where the dissociation of H2S is suppressed. Adding H2S...
1.7K
Ion-Exchange Chromatography
389
Ion-exchange chromatography, or IEC, is a technique for separating ions based on their affinity for the stationary phase. The stationary phase is a cross-linked polymer resin with covalently attached ionic functional groups. The functional groups can be either positively charged (cation exchangers) or negatively charged (anion exchangers). A cation exchanger consists of a polymeric anion and active cations, while an anion exchanger is a polymeric cation with active anions. The choice of...
389


