Synthesis Of Metal-organic Frameworks Research Articles

Carbon and metal based magnetic porous materials - Role in drug removal: A Comprehensive review

Development of effective adsorbents for the removal of contaminants from wastewater is indispensable due to increasing water scarcity and a lack of pure drinking water, which are prevailing as a result of rapid industrialization and population growth. Recently, the development of new adsorbents and their effective use without generating secondary waste is receiving huge consideration. In order to protect the environment from primary and secondary pollution, the development of adsorbents from wastes and their recycling have become conventional practices aimed at waste management. As a result, significant progress has been made in the synthesis of new porous carbon and metal-organic frameworks as adsorbents, with the objective of using them for the removal of pollutants. While many different kinds of pollutants are produced in the environment, drug pollutants are the most vicious because of their tendency to undergo significant structural changes, producing metabolites and residues with entirely different properties compared to their parent compounds. Chemical reactions involving oxidation, hydrolysis, and photolysis transform drugs. The resulting compounds can have detrimental effects on living beings that are present in soil and water. This review stresses the development of adsorbents with adjustable porosities for the broad removal of primary drug pollutants and their metabolites, which are formed as a result of drug transformations in environmental matrices. This keeps adsorbents from building up in the environment and prevents them from becoming significant pollutants in the future. Additionally, it stops secondary pollution caused by the deterioration of the used adsorbents. Focus on the development of effective adsorbents with flexible porosities allows for the complete removal of coexisting contaminants and makes a substantial contribution to wastewater management. In order to concentrate more on the development of flexible pore adsorbents, it is crucial to comprehend the milestones reached in the research and applications of porous magnetic adsorbents based on metal and carbon, which are discussed here.

Synthesis and Application of a pH-Responsive Functional Metal-Organic Framework: In Vitro Investigation for Delivery of Oridonin in Cancer Therapy.

Oridonin (Ori) is a naturally existing diterpenoid substance that mainly exists in the Chinese medicinal plant Rabdosia rubescens. It was previously found to possess intriguing biological properties; however, the quick clearance from plasma and limited solubility in water restricts its use as a drug. Several metal-organic frameworks (MOFs), having big surfaces and large pores, have recently been considered promising drug transporters. The zeolitic imidazolate framework-8 (ZIF-8), a form of MOF consisting of 2-methylimidazole with zinc ions, is structurally stable under physiologically neutral conditions, while it can degrade at low pH values such as in tumor cells. Herein, a nanosized drug delivery system, Ori@ZIF-8, was successfully designed for encapsulating and transporting oridonin to the tumor site. The drug loading of the prepared Ori@ZIF-8 was 26.78%, and the particles' mean size was 240.5 nm. In vitro, the release of Ori@ZIF-8 exhibited acid sensitivity, with a slow release under neutral conditions and rapid release of the drug under weakly acidic conditions. According to the in vitro anti-tumor experiments, Ori@ZIF-8 produced higher cytotoxicity than free Ori and induced apoptosis in A549 cancer cells. In conclusion, Ori@ZIF-8 could be a potential pH-responsive carrier to accurately release more oridonins at the tumor site.

Thickness-controllable synthesis of metal-organic framework based hollow nanoflowers with magnetic core via liquid phase epitaxy for phosphopeptides enrichment

Thickness-controllable synthesis of metal-organic framework based hollow nanoflowers with magnetic core via liquid phase epitaxy for phosphopeptides enrichment

Synthesis of a novel cost-effective double-ligand Zr-based MOF via an inverted modulator strategy towards enhanced adsorption and photodegradation of tetracycline

Developing visible-light response photocatalysts with high activity and adsorption alongside sustainability is vitally important to environmental restoration. Here, we fabricated a novel metal organic framework (MOF) with cost-effective double-ligands (fumaric acid and 2-aminoterephthalic acid as ligand precursors, denoted as MA-MOF) via a facile solvothermal method. Specifically, crystalline [Zr6O4(OH)4(fumarate)6] (MOF-801) can be only formed with monocarboxylic acids as modulators. Therefore, in the construction of crystalline double-ligand MA-MOF, the absence of monocarboxylic acid modulators successfully prevents the formation of crystalline MOF-801. Instead, the crystalline double-ligand MA-MOF is formed. Properties of MA-MOFs including the surface area, porosity, charge transfer resistance, and energy level position can be adjusted via altering the ratio of ligands. The optimal sample, MA-MOF2 (prepared with a molar ratio of fumaric acid and 2-aminoterephthalic acid being 2:1), shows a total 94.6% removal of tetracycline via adsorption and photodegradation, far exceeding the corresponding single-ligand counterparts. This work proposes an innovative inverted modulator strategy for constructing double-ligand MOFs.

Efficient calcium sulfite oxidation treatment by a highly active iron-manganese bimetallic metal-organic frameworks (MOFs)

Calcium sulfite (CaSO3) oxidation is the key step in the resource utilization of flue gas desulfurization (FGD) ash waste. However, under natural conditions the oxidation rate of CaSO3 is very low, limiting its conversion into calcium sulfate, an acceptable product for construction material. This study was devoted to the investigation of the synthesis and performance of a bimetallic MOFs with potential catalytic activity, namely, Fe/Mn(BDC)(DMF,F) catalysts. A combination of techniques including SEM, EDS, XRD, FT-IR, etc. were used to characterize the catalysts. The excellent catalytic performance examined in a gas-liquid-solid three-phase oxidation system are due to the special flexible respiratory architecture and homogeneous distribution of active sites, which allows the reactants to fully contact with the catalyst. Mn incorporated in the backbone of the metal-organic framework significantly enriches the catalytic active species that participate in a radical chain reaction with activated SO32- as ·SO3-, which in turn generates the key radical ·SO5- that reacts with SO32- to form SO42-. In the presence of Fe/Mn(BDC)(DMF, F)-13, the oxidation ratio of CaSO3 could reach 90.71%, which is more than 30-fold compared to non-catalytic oxidation and almost 5 times the effects of the single metal Fe(BDC)(DMF, F) catalyst. In addition, the study of kinetics shows that the oxidation rate of Fe/Mn(BDC)(DMF,F)-13 can reach 0.042 mmol·L-1·s-1 with an apparent activation energy of 10.86 kJ/mol. The oxidation rate is mainly affected by reaction temperature, pH value, catalyst concentration, and air flow rate. This study provides a potentially sustainable way for utilization of CaSO3-containing desulfurization ash.

Solvent-Induced Structural Rearrangement in Ultrasound-Assisted Synthesis of Metal-Organic Frameworks.

Metal-organic frameworks (MOFs) are crystalline extended structures featuring permanent porosity, assembled from metal ions and organic ligands, often synthesized by the solvothermal method (50-260°C, 12-72h). Here, an alternative synthetic approach-solvent-induced structural rearrangement in ultrasound-assisted synthesis is presented. Six representative Zn-based MOFs, each composed of distinct secondary building units, are synthesized within 2-180min consuming less solvent (>0.03m) at room temperature. It is observed that ultrasonication induces the construction of a coordination network, and subsequent solvent exchange triggers structural rearrangement to yield MOFs of high crystallinity and porosity. Furthermore, the scalability of this method is demonstrated through the bulk synthesis of MOF-5, MOF-74, ZIF-8, and MFU-4l within 90min. The initiation of nucleation through ultrasound and the subsequent transformation induced by solvent exchange offer an alternative method for efficiently synthesizing MOFs in bulk, potentially broadening their range of applications.

Amino Functionality Enables Aqueous Synthesis of Carboxylic Acid-Based MOFs at Room Temperature by Biomimetic Crystallization.

Enzyme immobilization within metal-organic frameworks (MOFs) is a promising solution to avoid denaturation and thereby utilize the desirable properties of enzymes outside of their native environments. The biomimetic mineralization strategy employs biomacromolecules as nucleation agents to promote the crystallization of MOFs in water at room temperature, thus overcoming pore size limitations presented by traditional postassembly encapsulation. Most biomimetic crystallization studies reported to date have employed zeolitic imidazole frameworks (ZIFs). Herein, we expand the library of MOFs suitable for biomimetic mineralization to include zinc(II) MOFs incorporating functionalized terephthalic acid linkers and study the catalytic performance of the enzyme@MOFs. Amine functionalization of terephthalic acids is shown to accelerate the formation of crystalline MOFs enabling new enzyme@MOFs to be synthesized. The structure and morphology of the enzyme@MOFs were characterized by PXRD, FTIR, and SEM-EDX, and the catalytic potential was evaluated. Increasing the linker length while retaining the amino moiety gave rise to a family of linkers; however, MOFs generated with the 2,2'-aminoterephthalic acid linker displayed the best catalytic performance. Our data also illustrate that the pH of the reaction mixture affects the crystal structure of the MOF and that this structural transformation impacts the catalytic performance of the enzyme@MOF.

In-silico green toxicology approach toward discovering safer ligands for development of safe-by-design metal–organic frameworks

A vast variety of chemical compounds have been fabricated and commercialized, they not only result in industrial exposure during manufacturing and usage, but also have environmental impacts throughout their whole life cycle. Consequently, attempts to assess the risk of chemicals in terms of toxicology have never ceased. In-silico toxicology, also known as predictive toxicology, has advanced significantly over the last decade as a result of the drawbacks of experimental investigations. In this study, ProTox-III was applied to predict the toxicity of the ligands used for metal–organic framework (MOF) design and synthesis. Initially, 35 ligands, that have been frequently utilized for MOF synthesis and fabrication, were selected. Subsequently, canonical simplified molecular-input line-entry system (SMILES) of ligands were extracted from the PUBCHEM database and inserted into the ProTox-III online server. Ultimately, webserver outputs including LD50 and the probability of toxicological endpoints (cytotoxicity, carcinogenicity, mutagenicity, immunotoxicity, and ecotoxicity) were obtained and organized. According to retrieved LD50 data, the safest ligand was 5-hydroxyisophthalic. In contrast, the most hazardous ligand was 5-chlorobenzimidazole, with an LD50 of 8 mg/kg. Among evaluated endpoints, ecotoxicity was the most active and was detected in several imidazolate ligands. This data can open new horizons in design and development of green MOFs.

Investigating the Effect of Trace Levels of Manganese Ions During Solvothermal Synthesis of Massey University Framework-16 on CO2 Uptake Capacity.

The effects of impurities on reaction precursors for metal-organic framework (MOF) synthesis have not been studied in extensive detail. The impact of these impurities can be an important factor while considering scale-up of these materials. In this work, we study the apparently positive impact of the presence of manganese ions for the synthesis of a Co-based MOF, Massey University Framework-16 (MUF-16). The presence of a trace amount of manganese in the reaction mixture led to consistently high CO2 uptake across multiple batches. Characterization including X-ray diffraction, scanning electron microscopy, Fourier transform infrared-attenuated total reflectance, ultraviolet-visible spectroscopy, thermogravimetric analysis, X-ray photoelectron spectroscopy, and extended X-ray absorption fine structure spectroscopy led us to hypothesize that the differences in CO2 adsorption among materials with differing synthesis routes arise from variations in the local environment around the cobalt metal center. Aided by density functional theory calculations, we speculate that manganese ions get inserted into the structure during crystallization and act as catalysts for ligand substitution, improving the possibility for octahedral coordination of cobalt with the ligand, thus leading to Co-based pristine structures with higher CO2 uptakes.

In situ synthesis of porous metal-organic frameworks NH2-UiO-66 on tea stem biochar and application in odours adsorption

Multiple odour nuisance in livestock farming is a notorious problem that has a significant impact on the living environment of surrounding communities. Adsorbents based on metal-organic framework (MOF) materials show great promise for controlling odour pollution, as they offer a high specific surface area, a controllable structure and an abundance of active sites. However, the MOF formation process is prone to problems such as pore clogging or collapse and reduced porosity, which limits its further application. In this study, a series of odour adsorbents were prepared by in situ growth of NH2-UiO-66 on tea stem biochar (TSBC) using a hydrothermal method and named UiO (Zr)-TSBCx. The physical and chemical properties and composition of UiO (Zr)-TSBCx have been systematically characterized using SEM, TEM, XRD, FT-IR, N2 adsorption-desorption and XPS. The release of odours from the pig farm effluent was monitored using in-situ continuous Proton-Transfer-Reaction Mass Spectrometry (PTR-MS), and the obtained primary compositions were tested for further adsorption. In dynamic adsorption experiments focused on butyric acid, UiO (Zr)-TSBC2 showed a high adsorption capacity of 3.99 × 105 μg/g and exceptional structural stability. UiO (Zr)-TSBC2 showed variable adsorption efficiencies for different odorous gases, with the best performance for the removal of ammonia, toluene and butyric acid. It also demonstrated the ability to rapidly mitigate instantaneous high concentrations of hydrogen sulfide (H2S), methanethiol and toluene resulting from agitation. Additionally, based on the relationship between the adsorption amount and the structural characteristics of the adsorbent as well as the nature of the odours, a possible adsorption mechanism of UiO (Zr)-TSBC2 for a variety of odours released from pig farm effluent was proposed. This work demonstrates a novel approach to promote deodorization applications in livestock and poultry farming environments by the in-situ growth of NH2-UiO-66 on biochar prepared from tea stem.

A new FeS2/N-C nanoparticle from NH2-MIL-101 for high performance lithium ion batteries

Among multitudinous lithium storage electrode materials, transition metal sulfides have attracted widespread attention because of high theoretical capacity and wide availability. However, these anodes still suffer poor capacity retention and limited cycle life. Metal organic frameworks (MOFs) are important precursors for fabricating functional materials for energy conversion and storage. A study of their derivatization process is of great significance for the design of materials with specific functional properties. In this paper, a new FeS2/N-C nanoparticle is synthesized by calcination strategy from NH2-MIL-101 prepared by solvothermal method. Due to the coordination effect of nitrogen-doped carbon and special particle morphology, the synthesized FeS2/N-C nanoparticles have superior cycling stability and high reversible capacity. This work provides a better understanding of the carbonization process of MOFs and reveals the effect of N-doped and MOF synthesis time on transition metal sulfides.

MOFs-Based Materials with Confined Space: Opportunities and Challenges for Energy and Catalytic Conversion.

Metal-Organic Frameworks (MOFs) are a very promising material in the fields of energy and catalysis due to their rich active sites, tunable pore size, structural adaptability, and high specific surface area. The concepts of "carbon peak" and "carbon neutrality" have opened up huge development opportunities in the fields of energy storage, energy conversion, and catalysis, and have made significant progress and breakthroughs. In recent years, people have shown great interest in the development of MOFs materials and their applications in the above research fields. This review introduces the design strategies and latest progress of MOFs are included based on their structures such as core-shell, yolk-shell, multi-shelled, sandwich structures, unique crystal surface exposures, and MOF-derived nanomaterials in detail. This work comprehensively and systematically reviews the applications of MOF-based materials in energy and catalysis and reviews the research progress of MOF materials for atmospheric water harvesting, seawater uranium extraction, and triboelectric nanogenerators. Finally, this review looks forward to the challenges and opportunities of controlling the synthesis of MOFs through low-cost, improved conductivity, high-temperature heat resistance, and integration with machine learning. This review provides useful references for promoting the application of MOFs-based materials in the aforementioned fields.

CO2-Based Stable Porous Metal-Organic Frameworks for CO2 Utilization.

The transformation of carbon dioxide (CO2) into functional materials has garnered considerable worldwide interest. Metal-organic frameworks (MOFs), as a distinctive class of materials, have made great contributions to CO2 capture and conversion. However, facile conversion of CO2 to stable porous MOFs for CO2 utilization remains unexplored. Herein, we present a facile methodology of using CO2 to synthesize stable zirconium-based MOFs. Two zirconium-based MOFs CO2-Zr-DEP and CO2-Zr-DEDP with face-centered cubic topology were obtained via a sequential desilylation-carboxylation-coordination reaction. The MOFs exhibit excellent crystallinity, as verified through powder X-ray diffraction and high-resolution transmission electron microscopy analyses. They also have notable porosity with high surface area (SBET up to 3688 m2 g-1) and good CO2 adsorption capacity (up to 12.5 wt %). The resulting MOFs have abundant alkyne functional moieties, confirmed through 13C cross-polarization/magic angle spinning nuclear magnetic resonance and Fourier transform infrared spectra. Leveraging the catalytic prowess of Ag(I) in diverse CO2-involved reactions, we incorporated Ag(I) into zirconium-based MOFs, capitalizing on their interactions with carbon-carbon π-bonds of alkynes, thereby forming a heterogeneous catalyst. This catalyst demonstrates outstanding efficiency in catalyzing the conversion of CO2 and propargylic alcohols into cyclic carbonates, achieving >99% yield at room temperature and atmospheric pressure conditions. Thus, this work provides a dual CO2 utilization strategy, encompassing the synthesis of CO2-based MOFs (20-24 wt % from CO2) and their subsequent application in CO2 capture and conversion processes. This approach significantly enhances overall CO2 utilization.

A Robust Pyrazolate Metal-Organic Framework for Efficient Catalysis of Dehydrogenative C-O Cross Coupling Reaction.

Construction of robust heterogeneous catalysts with atomic precision is a long-sought pursuit in the catalysis field due to its fundamental significance in taming chemical transformations. Herein, we present the synthesis of a single-crystalline pyrazolate metal-organic framework (MOF) named PCN-300, bearing a lamellar structure with two distinct Cu centers and one-dimensional (1D) open channels when stacked. PCN-300 exhibits exceptional stability in aqueous solutions across a broad pH range from 1 to 14. In contrast, its monomeric counterpart assembled through hydrogen bonding displays limited stability, emphasizing the role of Cu-pyrazolate coordination bonds in framework robustness. Remarkably, the synergy of the 1D open channels, excellent stability, and the active Cu-porphyrin sites endows PCN-300 with outstanding catalytic activity in the cross dehydrogenative coupling reaction to form the C-O bond without the "compulsory" ortho-position directing groups (yields up to 96%), outperforming homogeneous Cu-porphyrin catalysts. Moreover, PCN-300 exhibits superior recyclability and compatibility with various phenol substrates. Control experiments reveal the synergy between the Cu-porphyrin center and framework in PCN-300 and computations unveil the free radical pathway of the reaction. This study highlights the power of robust pyrazolate MOFs in directly activating C-H bonds and catalyzing challenging chemical transformations in an environmentally friendly manner.

Heterogeneous strategy constructing a built-in electric field: CoP/FeP bifunctional electrode for overall water splitting

Development of non-noble bifunctional electrocatalysts for the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) are of great significance under alkaline electrolytes for overall water splitting. In this work, CoP/FeP has been designed and constructed in situ on carbon fiber paper by using the bimetallic metal organic frameworks (MOFs) synthesis strategy. The heterogeneous CoP/FeP displays excellent catalytic activities in both HER and OER of the fully hydrolyzed semi-reaction. Remarkably, CoP/FeP is applied as the bifunctional electrode in anode and cathode to construct an overall water splitting apparatus, resulting in the low cell voltage and excellent stability. The exceptional electrocatalytic performance may be mainly attributed to the heterogeneous interface, which constructs a built-in electric field to provide electron to Co with electron-rich structure, resulting in the strong adsorption of H and weak adsorption of O2 on Co. This study provides an effective and controllable method for the design of self-supporting bimetal phosphide catalysts.

Removal of Humic Acid by UiO-66(Zr) and MIL-100(Fe) Metal-Organic Frameworks (MOFs) Adsorption

The escalating presence of humic acid (HA) in aquatic systems poses significant ecological and potable water treatment challenges, altering the color, taste, and odor of water and fueling algal blooms that deplete oxygen levels to the detriment of aquatic life. Traditional techniques like coagulation-flocculation, membrane filtration, oxidation fall short in efficiency due to its small fraction of HA. This study confronts the pervasive issue of HA contamination by leveraging the advanced properties of metal-organic frameworks (MOFs). In this work, two representative MOFs are synthesized and well characterized. Then, their capability for removal HA by adsorption process in water for HA treatment are detailed evaluated. The findings from this research extend beyond academic curiosity, offering actionable insights for water treatment facilities and environmental management agencies. The synthesis of MOFs which are UiO-66(Zr), MIL-100(Fe). Each MOFs have been applied to remove HA by adsorption under different condition. The effect of contacting time, initial pH, adsorbent dosage has been evaluated. After adsorption experiment, MOF samples prepared to dry and went through characterization. Removal of HA by MOF adsorption showed UiO-66(Zr) and MIL-100(Fe) examined rapid reaching equilibrium state with 10-15 min. Among various pH conditions, UiO-66(Zr) and MIL-100(Fe) showed the highest adsorption capacity under acidic conditions. MIL-100(Fe) achieves a higher maximum adsorption capacity than MIL-100(Fe). MOF after adsorption samples went through characterizations and their remained characteristics indicating the adsorption not affected the structure of the MOFs.

Synthesis of HER-capable cobalt metal organic framework using a straightforward reflux method and a thorough spectroscopic and theoretical analysis

A Cobalt MOF was obtained under reflux using aqueous methanol. The Cobalt MOF was synthesized using Cobalt (II) perchlorate hexahydrate and 1,3,5-Benzenetricarboxylic Acid (BTC) in a methanol mixed with double distilled water as a solvent under reflux condition for 2–3 h at 60–65 °C. The reddish solution obtained was filtered and kept in the refrigerator for almost 24 h. A crystal suitable for SC-XRD was obtained and the XRD analysis confirmed the polymeric structure of the Co-BTC. All the other analysis such as FTIR, Thermal analysis and FESEM of Co-BTC was carried out. Further, the efficacy of it as a potential catalyst towards HER was explored. The theoretical study assisted, and the data suggests that low band gap of the MOF possibly favors its efficacy in the Hydrogen Evolution Reaction (HER).

One-pot synthesis of multivariate porphyrinic metal-organic frameworks with the insertion of metallobipyridine and the cooperative catalysis for carbonyl hydrosilylation

A series of multivariate porphyrinic metal-organic frameworks with the insertion of bipyridine were obtained via one-pot synthesis. The single Pt site was introduced into the bipyridine linker of BPy@Co-PCN-224 through post-synthetic metalation. The resultant Pt(BPy)Cl2@M-PCN-224, especially when M was Co(II), could efficiently promote carbonyl hydrosilylation with a turnover number up to 13,140 based on Pt and could be recycled and reused for at least 6 times without a noticeable decrease of activity. Mechanistic studies based on in situ UV–vis, FT-IR and 1H NMR spectra, and kinetic isotope effect (KIE) experiments disclosed that the catalytic reaction was accomplished by the cooperative catalysis of Pt(BPy)Cl2 and Co-PCN-224, in which Pt(BPy)Cl2 was the catalytically active center and meanwhile the Co-PCN-224 could condense and increase the concentrations of ketone molecules in its inner cavities through the interactions between Co-porphyrin and carbonyl group. The plausible reaction pathway was proposed based on density functional theory calculations.

나노 크기의 금속 유기 골격체, ZIF-8 합성을 위한 이온성 액체 마이크로에멀젼 합성법의 체계적 연구

Porous Metal-Organic Frameworks (MOFs) are composed of metal ions and organic ligands. Recently, nano-sized MOFs have been widely utilized in biomedical fields, including biosensing and drug delivery. Researchers are primarily focusing on reducing their particle sizes to the nanoscale with a uniform size distribution. An ionic liquid microemulsion, the one of the MOF synthesis mehtods is in the limelight as an effective way with the following advantages: grain size uniformity and eco-friendliness. In this work, systematic study to control grain size, morphology, and yield of ZIF-8 (Zeolitic Imidazolate Framework-8) through ionic liquid microemulsion method was conducted in the new systems ‘water / surfactant (TX-100 or AOT) / CnmimX (n, the number of carbon = 2, 3, 4, 6, 8, 10 / X = Cl, Br, I)’. Furthermore, not only how the type of anion of ionic liquids, the length of carbon chain in them, the type of surfactants and the mass ratio change of the components affect the ZIF-8 synthesis results, respectively, was analyzed quantitatively through several characterization methods such as PXRD, TEM, DLS and FT-IR. Through this study, we aim to shed light on the infinite possibility of ionic liquid microemulsion method to synthesize desired size of nano-size MOF with uniformity.

Two dimensional Co-based metal organic framework for selective adsorption of Congo red from wastewater

Metal Organic Frameworks (MOFs) are promising candidates for adsorptive removal of dyes. Nevertheless, the synthesis of crystalline MOFs is a challenging task in achieving selective dye removal while ensuring efficient reusability. Herein, Co-MOF was synthesized by the solvothermal method and investigated using X-ray single crystallography, PXRD, IR and thermogravimetric analysis. Moreover, Co-MOF exhibits excellent removal efficiency towards Congo red. The maximum adsorption of Congo red by Co-MOF after optimizing parameters such as the effect of dye concentration, adsorbent dosages and pH was reached 974.86 mg/g. It is observed that the adsorption process follows the pseudo-second order kinetics and the adsorption isotherm fits well with the Langmuir model indicating complex adsorption process. The H-bonding, π-π interaction and electrostatic interaction play a crucial role in the adsorption mechanism. The Co-MOF has a significant recycling performance of 879.85 mg/g even after five cycles, showing potential application in wastewater treatment and developing a new class considering sustainable environment.