有效的Hg(II) 通过化学吸附通过易于部分连接体替换策略通过l-氨酸修饰的UiO-66去除
Zeming Dai1, Xuan Zhou1, Yuting Lin1
1College of Environmental Science and Engineering, Yangzhou University, Yangzhou 225000 PR China.
Journal of colloid and interface science
|January 16, 2025
概括
一种新的UiO-66-l-cys材料显示了水中的 (Hg(II)) 的显著增强吸附能力. 这一进步为重金属污染处理提供了具有成本效益和高效的解决方案.
科学领域:
- 材料科学 材料科学 材料科学
- 环境化学环境化学
- 纳米技术纳米技术
背景情况:
- 重金属污染,特别是 (Hg II),对水生生态系统和人类健康构成重大威胁.
- 传统的去除的方法往往涉及复杂的过程和高成本.
- 开发高效且具有成本效益的吸附材料对于环境修复至关重要.
研究的目的:
- 为了合成一种改性UiO-66材料 (UiO-66-l-cys),增强了Hg的吸附能力.
- 为了研究UiO-66-l-cys的吸附机制和去除功能的性能.
- 评估用于实际应用的开发材料的稳定性和成本效益.
主要方法:
- 简单的两步的部分连接体替代策略,用于UiO-66-l-cys合成.
- 吸附实验以确定Hg的吸收能力和性能.
- 兰木尔吸附模型和热力学研究.
- 进行X射线光电子光谱 (XPS) 和密度函数理论 (DFT) 计算以阐明吸附机制.
主要成果:
- 与原始UIO-66.6相比,UIO-66-l-cys的最大理论吸附能力为1321.4mg/g的Hg{}II,增加了20倍.
- 吸附是一种自发的,内热过程,在更高的温度下容量增加.
- XPS和DFT证实了硫 (SH) 和氨基 (NH2) 基在Hg (II) 结合中的关键作用.
- 该材料表现出极好的循环稳定性,在五个循环后,容量仅下降了2.7%.
结论:
- UiO-66-l-cys是一种高效的吸附剂,用于从水中去除Hg(II).
- 合成策略简单,具有成本效益,并且避免了复杂的化学过程.
- 这种材料在处理重金属污染方面具有很大的实际应用潜力.
相关概念视频
Extraction: Advanced Methods
407
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...
407
Ion-Exchange Chromatography
348
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...
348
Ion Exchange
537
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...
537
Metal-Ligand Bonds
20.5K
The hemoglobin in the blood, the chlorophyll in green plants, vitamin B-12, and the catalyst used in the manufacture of polyethylene all contain coordination compounds. Ions of the metals, especially the transition metals, are likely to form complexes.
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
20.5K
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
1.8K
Radical substitution reactions can be used to remove functional groups from molecules. The hydrogenolysis of alkyl halides is one such reaction, where the weak Sn–H bond in tributyltin hydride reacts with alkyl halides to form alkanes. Here, the reagent Bu3SnH yields tributyltin halide as a byproduct.
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation...
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation...
1.8K
Acid Halides to Ketones: Gilman Reagent
2.7K
Lithium dialkyl cuprate, also known as Gilman reagents, selectively reduces acid halides to ketones. The acid chloride is treated with Gilman reagent at −78 °C in the presence of ether solution to produce a ketone in good yield.
As shown below, the mechanism proceeds in two steps. First, one of the alkyl groups of the reagent acts as a nucleophile and attacks the acyl carbon of the acid chloride to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen...
As shown below, the mechanism proceeds in two steps. First, one of the alkyl groups of the reagent acts as a nucleophile and attacks the acyl carbon of the acid chloride to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen...
2.7K


