Highly effective and fast removal of anionic carcinogenic dyes via an In3-cluster-based cationic metal-organic framework with nitrogen-rich ligand

被引:44
作者
Liu, Xinyao [1 ]
Liu, Bing [1 ]
Eubank, Jarrod F. [2 ]
Liu, Yunling [1 ]
机构
[1] Jilin Univ, Coll Chem, State Key Lab Inorgan Synth & Preparat Chem, Changchun 130012, Peoples R China
[2] Florida Southern Coll, Dept Chem Biochem & Phys, 111 Lake Hollingsworth Dr, Lakeland, FL 33801 USA
基金
中国国家自然科学基金;
关键词
SELECTIVE ADSORPTION; MOF; PERFORMANCE; WATER; COORDINATION; SEPARATION; CAPACITY; STORAGE; FUNCTIONALIZATION; ADSORBENTS;
D O I
10.1039/c9qm00644c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this work, highly effective and rapid removal of anionic carcinogenic organic dye molecules is achieved through the use of a novel cationic metal-organic framework (MOF). The MOF is constructed using a nitrogen-rich triangular organic ligand, 4,4 ',4 ''-s-triazine-1,3,5-triyltri-p-aminobenzoate (H(3)TATAB), and trinuclear 6-connected In-3-cluster secondary building units (SBUs), [In3O(TATAB)(2)(H2O)(3)](NO3)center dot(DMA)(15) (In-TATAB), which gives a structure exhibiting a new topology. As the formula indicates, In-TATAB is inherently cationic due to the [In3O(COO-)(6)](+) units, which thus favors interaction with anionic guests. Several organic dye molecules of varying charge and size, such as acid chrome blue K, acid red 26, congo red, direct black 38 and, orange II, were used to test the sequestration potential of the MOF material. In addition to electrostatic attraction, it is shown that hydrogen-bonding originating from the highly functional bridging ligand and terminal H2O ligands enhance the interactions between the framework and guest dye molecules, suggesting its potential use for the removal of anionic organic pollutants.
引用
收藏
页码:182 / 188
页数:7
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