scholarly journals Metal–organic frameworks (MOFs) based nanofiber architectures for the removal of heavy metal ions

RSC Advances ◽  
2022 ◽  
Vol 12 (3) ◽  
pp. 1433-1450
Author(s):  
Heja Ibrahim Adil ◽  
Mohammad R. Thalji ◽  
Suhad A. Yasin ◽  
Ibtisam A. Saeed ◽  
Mohammed A. Assiri ◽  
...  
Keyword(s):  
Heavy Metal ◽  
Metal Ions ◽  
Heavy Metal Ions ◽  
Metal Organic Frameworks ◽  
Chemical Properties ◽  
High Specific Surface Area ◽  
High Porosity ◽  
Metal Organic ◽  
Physical And Chemical ◽  
And Chemical Properties

Metal–organic frameworks (MOFs) are promising and effective materials for removing heavy metal ions from contaminated water owing to their high porosity, remarkable physical and chemical properties, and high specific surface area.

Functional group effect of isoreticular metal–organic frameworks on heavy metal ion adsorption

2018 ◽  
Vol 42 (11) ◽  
pp. 8864-8873 ◽  
Author(s):  
Leili Esrafili ◽  
Vahid Safarifard ◽  
Elham Tahmasebi ◽  
M. D. Esrafili ◽  
Ali Morsali
Keyword(s):  
Heavy Metal ◽  
Metal Ions ◽  
Metal Ion ◽  
Heavy Metal Ions ◽  
Functional Group ◽  
Metal Organic Frameworks ◽  
Ion Adsorption ◽  
Group Effect ◽  
Metal Ion Adsorption ◽  
Metal Organic

We examined adsorption behavior of some MOFs having different functional groups in their pillar structures for adsorption of some heavy metal ions.

Tuning Packing, Structural Flexibility, and Porosity in 2D Metal–Organic Frameworks by Metal Node Choice

2019 ◽  
Vol 72 (10) ◽  
pp. 797 ◽  
Author(s):  
Witold M. Bloch ◽  
Christian J. Doonan ◽  
Christopher J. Sumby
Keyword(s):  
Structural Changes ◽  
Metal Organic Frameworks ◽  
Chemical Properties ◽  
Complete Removal ◽  
Structural Flexibility ◽  
X Ray Diffraction ◽  
Metal Centre ◽  
Metal Organic ◽  
Physical And Chemical ◽  
And Chemical Properties

Understanding the key features that determine structural flexibility in metal–organic frameworks (MOFs) is key to exploiting their dynamic physical and chemical properties. We have previously reported a 2D MOF material, CuL1, comprising five-coordinate metal nodes that displays exceptional CO2/N2 selectively (L1=bis(4-(4-carboxyphenyl)-1H-pyrazolyl)methane). Here we examine the effect of utilising six-coordinate metal centres (CoII and NiII) in the synthesis of isostructural MOFs from L1, namely CoL1 and NiL1. The octahedral geometry of the metal centre within the MOF analogues precludes an ideal eclipse of the 2D layers, resulting in an offset stacking, and in certain cases, the formation of 2-fold interpenetrated analogues β-CoL1 and β-NiL1. We used a combination of thermogravimetric analysis (TGA), and powder and single crystal X-ray diffraction (PXRD and SCXRD) to show that desolvation is accompanied by a structural change for NiL1, and complete removal of the coordinated H2O ligands results in a reduction in long-range order. The offset nature of the 2D layers in combination with the structural changes impedes the adsorption of meaningful quantities of gases (N2, CO2), highlighting the importance of a five-coordinate metal centre in achieving optimal pore accessibility for this family of flexible materials.

Recent Progress in the Removal of Heavy Metal Ions from Water Using Metal‐Organic Frameworks

2020 ◽  
Vol 5 (1) ◽  
pp. 124-146 ◽  
Author(s):  
Hossein Shayegan ◽  
Gomaa A. M. Ali ◽  
Vahid Safarifard
Keyword(s):  
Heavy Metal ◽  
Metal Ions ◽  
Heavy Metal Ions ◽  
Recent Progress ◽  
Metal Organic Frameworks ◽  
Metal Organic

scholarly journals Fluorinated Organic Porous Materials

2019 ◽  
Vol 01 (01) ◽  
pp. 019-029 ◽  
Author(s):  
Zhenglin Zhang ◽  
Ognjen Š. Miljanić
Keyword(s):  
Porous Materials ◽  
Organic Molecules ◽  
Metal Organic Frameworks ◽  
Molecular Crystals ◽  
Chemical Properties ◽  
Physical And Chemical Properties ◽  
Metal Organic ◽  
Physical And Chemical ◽  
And Chemical Properties

Fluorine is in many aspects unique among the elements, and its incorporation into organic molecules can dramatically change their physical and chemical properties. This minireview will survey the existing classes of fluorinated porous materials, with a particular focus on all-organic porous materials. We will highlight our work on the preparation and study of metal–organic frameworks and porous molecular crystals derived from extensively fluorinated rigid aromatic pyrazoles and tetrazoles. Where possible, comparisons between fluorinated and nonfluorinated materials will be made.

Engineering Isoreticular 2D Metal–Organic Frameworks with Inherent Structural Flexibility

2017 ◽  
Vol 70 (5) ◽  
pp. 566 ◽  
Author(s):  
Alexandre Burgun ◽  
Witold M. Bloch ◽  
Christian J. Doonan ◽  
Christopher J. Sumby
Keyword(s):  
Metal Organic Frameworks ◽  
Mixed Valence ◽  
Chemical Properties ◽  
Fine Tuning ◽  
Gate Opening ◽  
Sterically Demanding ◽  
Metal Organic ◽  
Structure Metrics ◽  
Physical And Chemical ◽  
And Chemical Properties

The chemical mutability of metal–organic frameworks (MOFs) is an advantageous feature that allows fine-tuning of their physical and chemical properties. Herein, we report the successful isoreticulation of a MOF with an outstanding gas selectivity for CO2 versus N2: [Cu(L1)(H2O)]·xS (CuL1), where H2L1 = bis(4-(4-carboxyphenyl)-1H-pyrazolyl)methane) and S = solvate. By modifying the steric bulk and length of the original ligand, we synthesised three new MOFs with 2D networks isoreticular to CuL1, namely [Cu(L1Me)(H2O)]·xS (CuL1Me), [Cu(L2)(H2O)]·xS (CuL2), and [Cu(L2Me)(H2O)]·xS (CuL2Me) (where H2L1Me = bis(4-(4-carboxyphenyl)-3,5-dimethyl-1H-pyrazolyl)methane, H2L2 = bis(4-(4-carboxyphenyl)-(ethyne-2,1-yl)-1H-pyrazolyl)methane, and H2L2Me = bis(4-(4-carboxyphenyl)-(ethyne-2,1-yl)-3,5-dimethyl-1H-pyrazolyl)methane). Depending on the steric hindrance and structure metrics of the organic links, staggered and eclipsed arrangements of 2D 44 net layers were obtained. The anisotropy of the pore dimensions is proportional to the linker length (L2 and L2Me), which when increased, renders these materials non-porous. However, the more sterically demanding ligand L1Me gives a material that shows gate-opening behaviour in response to a CO2 absorbate. The synthesis and structure of an unexpected mixed-valence CuII/CuI 3D MOF, Cu3[Cu(L2Me)2]2(H2O)4]·xS (Cu5(L2Me)4), containing an unusual trimeric CuII node are also reported.

scholarly journals Novel Mixed Matrix Membranes Based on Polymer of Intrinsic Microporosity PIM-1 Modified with Metal-Organic Frameworks for Removal of Heavy Metal Ions and Food Dyes by Nanofiltration

Membranes ◽  
2021 ◽  
Vol 12 (1) ◽  
pp. 14
Author(s):  
Anna Kuzminova ◽  
Mariia Dmitrenko ◽  
Andrey Zolotarev ◽  
Aleksandra Korniak ◽  
Daria Poloneeva ◽  
...  
Keyword(s):  
Heavy Metal ◽  
Metal Ions ◽  
Heavy Metal Ions ◽  
High Efficiency ◽  
Metal Organic Frameworks ◽  
Mixed Matrix Membranes ◽  
Polymer Of Intrinsic Microporosity ◽  
Food Dyes ◽  
Metal Organic ◽  
Intrinsic Microporosity

Nowadays, nanofiltration is widely used for water treatment due to its advantages, such as energy-saving, sustainability, high efficiency, and compact equipment. In the present work, novel nanofiltration membranes based on the polymer of intrinsic microporosity PIM-1 modified by metal-organic frameworks (MOFs)—MIL-140A and MIL-125—were developed to increase nanofiltration efficiency for the removal of heavy metal ions and dyes. The structural and physicochemical properties of the developed PIM-1 and PIM-1/MOFs membranes were studied by the spectroscopic technique (FTIR), microscopic methods (SEM and AFM), and contact angle measurement. Transport properties of the developed PIM-1 and PIM-1/MOFs membranes were evaluated in the nanofiltration of the model and real mixtures containing food dyes and heavy metal ions. It was found that the introduction of MOFs (MIL-140A and MIL-125) led to an increase in membrane permeability. It was demonstrated that the membranes could be used to remove and concentrate the food dyes and heavy metal ions from model and real mixtures.

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