快速,可逆和选择性离子交换的三维离子共价有机框架
Zonglong Li1, Hui Li1, Xinyu Guan1
1State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, Jilin University , Changchun 130012, P. R. China.
Journal of the American Chemical Society
|November 29, 2017
概括
研究人员开发了具有高表面积和二氧化碳吸收的正电荷3D离子共价有机框架 (COF). 这些新型COF显示出有效的离子交换能力,用于核废物清除和污染物捕获.
科学领域:
- 材料科学
- 纳米技术
- 化学学
背景情况:
- 共价有机框架 (COF) 是具有越来越多应用的功能材料.
- 三维 (3D) COF 的发展仍然有限,大多数现有框架都是中立的.
- 需要具有定制性质的先进COF,例如电荷和孔隙性.
研究的目的:
- 引入合成多孔,正电荷的3D离子COF的总体策略.
- 研究这些新型COF的结构特征和气体吸收特性.
- 评估合成的3D离子COF用于环境修复的离子交换能力.
主要方法:
- 在合成过程中将阴离子单体纳入框架.
- 3D COF结构的特征,包括孔隙性和表面积.
- 测试二氧化碳吸附能力.
- 使用核废物离子和离子污染物模型评估离子交换性能.
主要成果:
- 成功设计和合成多孔正电3D离子COF.
- 三维COF表现出一个三重互穿的钻石网结构.
- 取得了令人印象深刻的表面积和显著的二氧化碳吸收.
- 证明了有效的离子交换特性,包括可逆去除核废物离子和对离子污染物的尺寸选择性捕获.
结论:
- 已经制定了一种创建3D离子COF的新策略.
- 这些3D离子COF显示出高表面积,二氧化碳吸收和多功能离子交换功能.
- 这项工作为利用3D COF作为废物管理和污染物控制的先进离子交换材料开辟了新的途径.
更多相关视频
相关概念视频
Ion Exchange
1.3K
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...
1.3K
Ion-Exchange Chromatography
2.3K
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...
2.3K
Ionic Crystal Structures
18.2K
Ionic crystals consist of two or more different kinds of ions that usually have different sizes. The packing of these ions into a crystal structure is more complex than the packing of metal atoms that are the same size.
Most monatomic ions behave as charged spheres, and their attraction for ions of opposite charge is the same in every direction. Consequently, stable structures for ionic compounds result (1) when ions of one charge are surrounded by as many ions as possible of the opposite...
Most monatomic ions behave as charged spheres, and their attraction for ions of opposite charge is the same in every direction. Consequently, stable structures for ionic compounds result (1) when ions of one charge are surrounded by as many ions as possible of the opposite...
18.2K
Formation of Complex Ions
26.3K
A type of Lewis acid-base chemistry involves the formation of a complex ion (or a coordination complex) comprising a central atom, typically a transition metal cation, surrounded by ions or molecules called ligands. These ligands can be neutral molecules like H2O or NH3, or ions such as CN− or OH−. Often, the ligands act as Lewis bases, donating a pair of electrons to the central atom. These types of Lewis acid-base reactions are examples of a broad subdiscipline called coordination...
26.3K
Ionic Bonding and Electron Transfer
50.4K
Ions are atoms or molecules bearing an electrical charge. A cation (a positive ion) forms when a neutral atom loses one or more electrons from its valence shell, and an anion (a negative ion) forms when a neutral atom gains one or more electrons in its valence shell. Compounds composed of ions are called ionic compounds (or salts), and their constituent ions are held together by ionic bonds: electrostatic forces of attraction between oppositely charged cations and anions.
50.4K
Extraction: Advanced Methods
1.2K
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...
1.2K


