从废水中通过电化学选择性回收通过合结和电荷储存回收废水
Fubing Yao1, Wanchao Li1, Zhigong Liu1
1School of Metallurgy and Environment, Central South University, Changsha 410083, China; State Key Laboratory of Advanced Metallurgy for Non-ferrous Metals, Changsha 410083, China; Chinese National Engineering Research Center for Control & Treatment of Heavy Metal Pollution, Changsha 410083, China.
Water research
|January 13, 2024
概括
从废水中电化学 (NH4+) 的回收得到了显著的改进,使用了一种新的GO/V2O5电极. 这种方法实现了高存储能力和选择性,克服了当前技术的局限性.
科学领域:
- 环境科学 环境科学
- 材料科学 材料科学 材料科学
- 电化学 电化学 电化学
背景情况:
- 电化学 (NH4+) 储存 (EAS) 是废水回收的关键.
- 目前的EAS方法面临着低容量和选择性的挑战.
- 这些局限性阻碍了广泛的工程应用.
研究的目的:
- 开发一种高效和选择性的NH4+从废水中回收的方法.
- 为了研究增强NH4+储存背后的机制.
- 为改进NH4+回收技术提供准则.
主要方法:
- 自组装的双层复合电极 (GO/V2O5) 的制造.
- 使用密度函数理论 (DFT) 阐明机制.
- 进行物理和电化学分析.
主要成果:
- 达到234.7毫克Ng-1的NH4+储存能力,比活性炭高100倍以上.
- 由于电子捐赠能力和降低屏障,DFT揭示了增强的NH4+扩散.
- 增加的膜间距和ECSA通过结和电荷储存促进了NH4+的插入.
结论:
- 该GO/V2O5电极可实现高效和选择性的电化学NH4+回收.
- 结合和电荷储存的协同效应推动了卓越的性能.
- 这项研究为设计用于废水NH4+整治的先进材料提供了基础.
相关概念视频
Ion Exchange
592
Ion exchange chromatography separates charged molecules from a solution by reversibly exchanging them with mobile, or 'active', ions associated with the oppositely charged stationary phase. This method can be used to separate ions, soften and deionize water, and purify solutions. The polymers comprising the ion-exchange column are high-molecular-weight and chemically stable polymers, crosslinked to be porous and essentially insoluble. They are also functionalized with either acidic or...
592
Titration of a Weak Base with a Strong Acid
5.3K
The titration curve of a weak base like ammonia with a strong acid like hydrochloric acid is the mirror image of the titration curve of a weak acid with a strong base.
Using the ICE table and substituting the Kb value, we calculate the initial pH of 50 mL of 0.1 M ammonia to be 11.11. Addition of 25 mL of 0.1 M hydrochloric acid to this solution of ammonia results in a buffer with an equal concentration of ammonia and ammonium ions. The pH of this buffer can be calculated by substituting these...
Using the ICE table and substituting the Kb value, we calculate the initial pH of 50 mL of 0.1 M ammonia to be 11.11. Addition of 25 mL of 0.1 M hydrochloric acid to this solution of ammonia results in a buffer with an equal concentration of ammonia and ammonium ions. The pH of this buffer can be calculated by substituting these...
5.3K
Hydrogen Bonds
8.5K
A hydrogen bond is formed when a weakly positive hydrogen atom already bonded to one electronegative atom (for example, the oxygen in the water molecule) is attracted to another electronegative atom from another polar molecule, such as water (H2O), hydrogen fluoride (HF), or ammonia (NH3). The huge electronegativity difference between the H atom (2.1) and the atom to which it is bonded (4.0 for an F atom, 3.5 for an O atom, or 3.0 for an N atom), combined with the very small size of an H atom...
8.5K
Preparation of Amines: Alkylation of Ammonia and Amines
3.4K
Alkylation is one of the methods used to prepare amines. Direct alkylation of ammonia or a primary amine with an alkyl halide gives polyalkylated amines along with a quaternary ammonium salt through successive SN2 reactions. This process of making the quaternary salt through the direct alkylation method is called exhaustive alkylation.
Each alkylation step makes the nitrogen center more nucleophilic, which triggers successive alkylations until a quaternary ammonium salt is formed. Considering...
Each alkylation step makes the nitrogen center more nucleophilic, which triggers successive alkylations until a quaternary ammonium salt is formed. Considering...
3.4K
Common Ion Effect
41.7K
Compared with pure water, the solubility of an ionic compound is less in aqueous solutions containing a common ion (one also produced by dissolution of the ionic compound). This is an example of a phenomenon known as the common ion effect, which is a consequence of the law of mass action that may be explained using Le Châtelier’s principle. Consider the dissolution of silver iodide:
41.7K
Titration in Nonaqueous Solvents
805
Most acid-base titrations are performed in an aqueous medium. In aqueous titrations, water competes with weaker acids or bases for proton donation or acceptance, leading to ambiguous endpoints in the titration curve. Water also affects the partial ionization of weak acids or bases. For example, water accepts a proton from acetic acid to form hydronium and acetate ions. The hydronium ion formed is a stronger acid than acetic acid, and the acetate ion is a stronger base than water. As a result,...
805


