共 47 条
Acyl amide-functionalized and water-stable iron-based MOF for rapid and selective dye removal
被引:27
作者:

Ghasempour, Hosein
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Tarbiat Modares Univ, Dept Chem, Fac Sci, POB 14117-13116, Tehran, Iran Tarbiat Modares Univ, Dept Chem, Fac Sci, POB 14117-13116, Tehran, Iran

Zarekarizi, Farnoosh
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机构:
Tarbiat Modares Univ, Dept Chem, Fac Sci, POB 14117-13116, Tehran, Iran Tarbiat Modares Univ, Dept Chem, Fac Sci, POB 14117-13116, Tehran, Iran

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机构:
[1] Tarbiat Modares Univ, Dept Chem, Fac Sci, POB 14117-13116, Tehran, Iran
基金:
美国国家科学基金会;
关键词:
METAL-ORGANIC FRAMEWORKS;
LOW-COST ADSORBENTS;
METHYLENE-BLUE;
ADSORPTION BEHAVIOR;
PURIFICATION;
NANOMATERIALS;
CONTAMINANTS;
METHANE;
D O I:
10.1039/d2ce00369d
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Multinuclear cluster-based metal-organic frameworks (MOFs) have shown excellent activity in toxic chemical removal from wastewater due to their high porosity, functionality and water stability. In this regard, a highly porous, water-stable Fe-MOF was fabricated and the efficiency of its acyl amide-functionalized pores for organic dye removal was investigated. Different anionic and cationic dyes including methyl orange (MO), methyl red (MR), congo red (CR), rose-bengal B (Ros B), rhodamine B (Rhod B) and methylene blue (MB) were applied to determine the Fe-MOF efficiency. The presence of acyl amide improves the host-guest interaction of the framework towards anionic dyes, specifically MO with an adsorption capacity of 232.5 mg g(-1). Interestingly, the Fe-MOF shows one of the fastest adsorptions of MO with a kinetic constant of 0.013 g mg(-1) min(-1) which is faster than those of some of the well-known MOFs such as UiO-66, MOF-235, MIL-53, MIL-101, UiO-66-NO2 and ZIF-67. The adsorption mechanism, uptake kinetics and selectivity of the framework for different dyes were also studied. Overall, water stable Fe-MOF with a high permanent porosity as well as rational decoration of pores with specific functions, improved the size and charge selective dye removal by the preferred H-bonding and pi-pi interactions.
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页码:4074 / 4084
页数:11
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