通过氨基功能化ZIF-8从水溶液中增强Cd(II) 的吸附和去除
Amir Khosravi1, Razieh Habibpour2, Maryam Ranjbar3
1Department of Chemical Technology, Iranian Research Organization for Science and Technology (IROST), Tehran, Iran.
Scientific reports
|May 10, 2024
概括
修改过乙烯基胺的酸伊米达酸框架-8 (ZIF-8-EDA) 有效地从水中去除离子. 这种增强的吸附剂在去除Cd2+方面表现出高效率和选择性,使其成为净化水的有前途材料.
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:
- 金属有机框架 (MOFs),特别是酸胺酸框架-8 (ZIF-8),是具有可调节性质的先进材料.
- 污染废水的重金属离子如 (Cd2+) 构成严重的环境和健康风险.
- 开发高效和选择性的吸附剂对于有效的重金属整治至关重要.
研究的目的:
- 合成和表征以乙二胺修饰的ZIF-8 (ZIF-8-EDA) 作为去除离子 (Cd2+) 的吸附剂.
- 研究ZIF-8-EDA对Cd2+的吸附性能,动力学和热力学.
- 评估ZIF-8-EDA对不同重金属离子的选择性.
主要方法:
- 使用XRD,FT-IR,BET,FE-SEM,EDS和TEM进行ZIF-8和ZIF-8-EDA的合成和表征.
- 批量吸附实验以确定最佳条件 (剂量,度,pH,接触时间).
- 使用兰木尔和弗洛因利希模型分析吸附数据,以及热力学研究.
主要成果:
- 对于Cd2+离子,ZIF-8-EDA的高去除效率为93.5%,超过了未经修改的ZIF-8 (89.7%).
- 兰穆尔模型最好地描述了吸附平衡,最大吸收能力为294.11 mg/g.
- 发现吸附是可行的,自发的和内热的,ZIF-8-EDA对Cd2+>Pb2+>Ni2+具有选择性.
结论:
- 乙二胺功能化显著提高了ZIF-8的Cd2+吸附性能.
- 性能改善归因于氨基功能组和金属离子之间的化学协调.
- ZIF-8-EDA是一种高效和选择性的吸附剂,用于从水溶液中去除.
相关概念视频
Colloidal precipitates
565
The high insolubility of some precipitates can result in an unfavorable relative supersaturation. This can lead to colloidal particles with a large surface-to-mass ratio, where adsorption is promoted. For instance, in the precipitation of silver chloride, silver ions are adsorbed on the surface of the colloidal particles, forming a primary layer. This layer attracts ions of opposite charge (such as nitrate ions), forming a diffuse secondary layer of adsorbed ions. This electric double layer...
565
Extraction: Advanced Methods
446
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...
446
Aryldiazonium Salts to Azo Dyes: Diazo Coupling
2.9K
The reaction of weakly electrophilic aryldiazonium (also called arenediazonium) salts with highly activated aromatic compounds leads to the formation of products with an —N=N— link, called an azo linkage. This reaction, presented in Figure 1, is known as diazo coupling and occurs without the loss of the nitrogen atoms of the aryldiazonium salt. Highly activated aromatic compounds such as phenols or arylamines favor the diazo coupling reaction. The coupling generally occurs at the...
2.9K


