Metal Organic Framework UiO-66 Research Articles

Synthesis of UiO-67 Metal-organic Frameworks (MOFs) and their Application as Antibacterial and Anticancer Materials

This study involved the synthesis of the UiO-67 metal-organic framework; UiO-67 is a well-known type of MOF obtained by coordinating the Zr6O4(OH)4 metal unit with the 4,42-biphenyldicarboxylate organic linker, using the hydrothermal technique. The novelty of the current work is to synthesize UiO-67 MOFs, and their application as biological agents for antibacterial and cancer cells. Subsequently, the composite material UiO-67 was subjected to a comprehensive characterization process involving Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), thermal gravimetric analyses (TGA) and surface area analysis, and the results showed the successful synthesis of the UiO-67 MOFs, with a high specific surface area of 1415 m2/g. The­­­ synthesized UiO-67 for its antibacterial properties tested against five pathogenic bacterial strains, which include three gram-positive and methicillin-resistant pairs including MRSA, S. aureus and Enterococcus faecalis, and Two gram-negative bacteria E. colli and S. typhimurium using the agar well diffusion method. These findings have shown enhanced, strong antibacterial activity against all the five used gram-positive and gram-negative bacterial strains. Furthermore, the anticancer efficacy of UiO-67 was evaluated on two distinct types of cancer cells: We are using MCF-7 (human breast cancer cell line) and HepG2 (human liver cancer cells). The experiments prove that UiO-67 has the potential of cytotoxicity against both Glioblastoma and H460 cancer lines with the ability to inhibit apoptosis at the same time.

Computational Exploration on Coupling Formic Acid Production with Propylene Synthesis via Catalytic Transfer Hydrogenation: The Role of CO2 beyond Reverse Water Gas Shift Reaction.

CO2-assisted propane dehydrogenation (CO2-ODHP) is emerging as an alternative route to the direct dehydrogenation of propane. Previous studies on CO2-ODHP have shown that the role of CO2 is to shift the reaction equilibrium toward the product side by consuming the produced H2 molecules via reverse water gas shift (RWGS) reaction. Since the ultimate fate of CO2 is to get reduced, we herein propose another pathway of CO2 reduction in the realm of CO2-ODHP─CO2 hydrogenation to formic acid (FA). With the objective of investigating the feasibility of this process, we, for the first time, carry out a computational investigation on coupling propane dehydrogenation with CO2 hydrogenation using a Ti-alkoxide-functionalized UiO-67 metal-organic framework. Analysis using the distortion/interaction model confirms that CO2 hydrogenation to FA is a preferred pathway over the RWGS reaction and hence can be realized in practice. Our study also highlights the importance of intersystem crossing, which provides an opportunity to access nonground state potential energy surfaces while undergoing chemical transformations. Again, subsequent addition of water molecules has shown to ease product desorption by 41 kcal/mol. Our study, therefore, hints at an unexplored role of CO2 beyond the RWGS reaction in oxidative propane dehydrogenation.

Capacity building in porous materials research for sustainable energy applications.

The project aimed to develop porous materials for sustainable energy applications, namely, hydrogen storage, and valorization of biomass to renewable fuels. At the core of the project was a training programme for Africa-based researchers in (i) the exploitation of renewable locally available raw materials; (ii) the use of advanced state-of-the-art techniques for the design and synthesis of porous materials (zeolites and metal-organic frameworks (MOFs)) for energy storage; and (iii) the valorization of sustainable low-value feedstock to renewable fuels. We found that compaction of the UiO-66 MOF at high pressure improves volumetric hydrogen storage capacity without any loss in gravimetric uptake, and experimentally demonstrated the temperature-dependent dynamic behaviour of UiO-66, which allowed us to propose an activation temperature of ≤ 150°C for UiO-66. Co-pelletization was used to fabricate UiO-66/nanofibre monoliths as hierarchical porous materials with enhanced usable (i.e. deliverable) hydrogen storage capacity. We clarified the use of naturally occurring kaolin as a source of silica and alumina species for zeolite synthesis. The kaolin-derived zeolite X was successfully used as a catalyst for the transesterification of Jatropha curcas oil (from non-edible biomass) to biodiesel. We also prepared porous composites (i.e. carbon/UiO-66, organoclay/UiO-66 and zeolite/carbon) that were successfully applied in electrochemical sensing.

Impact of the material hydroxylation on the possibility of pentane isomers separation by UiO-66 (Zr) MOF: A combined 2H NMR and MD study

The mobility of the pentane isomers in the hydroxylated UiO-66 metal-organic framework has been characterized. 2H NMR spectroscopy was applied to measure the jump rate of alkanes guest molecules between adjacent cages and estimate the diffusivity. It is inferred that the difference in diffusion coefficients defines the kinetic separation selectivity, which is higher for the linear alkanes. The adsorption of pentane isomers in UiO-66 has been modeled with molecular dynamics (MD) simulation. The adsorbed quantity of isopentane is higher than that for n-pentane, providing the possibility of separation with selectivity α ≈ 8 in stationary conditions. The impact of the UiO-66 MOF hydroxylation state on the mobility of pentane isomers has been characterized by comparison with results obtained for the dehydroxylated UiO-66 material. The hydroxylated state of UiO-66 MOF has 6-time higher separation selectivity for pentane isomers compared to its dehydroxylated state (αhyd ≈ 76). MD calculations show that hydroxylated UiO-66 MOF is more efficient, as the separation selectivity is 4 times lower in the dehydroxylated material. The UiO-66 hydroxylation effect is compared for the mobility of C4 and C5 alkanes. The optimal conditions for C4/C5 alkanes kinetic separation by UiO-66 MOF are established.

Accelerated thioanisole oxidation using partially β-brominated Cobalt(II) porphyrin heterogenized within UiO-66 scaffold

Heterogenization of a partially β-brominated cobalt (II) tetraphenylporphyrin complex (CoIITPPBr4) within the cavities of an UiO-66 (UiO stands for Universitetet i Oslo) metal-organic framework (MOF) using bottle-around-ship (BAS) strategy resulted in the formation of highly selective recoverable biomimetic catalyst (CoIITPPBr4@UiO-66). Integrating partial β-bromination with entrapment within the MOF host improved the porphyrin complex's stability and efficiency while preventing its deactivation owing to self-destruction. Under the influence of a heterogenized catalyst with a low active component loading, the selective oxidation of thioanisole (PhSMe) to methyl phenyl sulfoxide (PhSOMe) by hydrogen peroxide (H2O2) in acetonitrile (MeCN) solvent in the presence of imidazole (ImH) co-catalyst and acetic anhydride (Ac2O) activator was expedited significantly with an outstanding conversion (96.01 %) and selectivity (100 %). Also, the utilization of diverse analysis techniques verified the efficacious fabrication, as well as the stability and recyclability of the catalyst after four catalytic cycles.

Non-steroidal anti-inflammatory drugs adsorption from aqueous solution by MOFs MIL-100(Fe), ZIF-8 and UiO-66: Synthesis, characterization, and comparative study

Pharmaceutical products such as ibuprofen and naproxen pose a potencial risk to the environment and to the human health. In this context, it is necessary seek and implement new effective and low-cost technologies for water treatment such as adsorption. Metal-organic frameworks (MOFs) emerge as promising adsorbent materials due to their structural diversity and stability. The obtained MOFs were characterized by SEM/EDX, XRD, FTIR, N2 at 77 K, DLS, and PZC. According to the textural parameters, the obtained MOFs have the next surface areas: MIL-100 (Fe) 1359 m2, ZIF-8 357 m2 and UiO-66 1654 m2. Having this differences in surface areas, alongside the different PZC of each materials, affect the adsorption capacity. According to the experimental data UiO-66 and MIL-100(Fe) had the highest ibuprofen adsorption capacity (152.3 mg g-1) and naproxen adsorption capacity (278.3 mg g-1), respectively. On the other hand, ZIF-8 has the lowest adsorption capacity of ibuprofen and naproxen (85.4 and 78.9 mg g-1 respectively). It was found that the best-fitting model according to its R2 for all materials with both adsorbates was the Sips model. Moreover, all materials with all adsorbates, except for UiO-66 with naproxen, reached equilibrium within the first 120 min and fitted the pseudo-second order model. According to thermodynamic parameters and analysis of fitted kinetic models, it was determined that during adsorption, a combination of physical and chemical phenomena occurs, from which the following interactions are proposed as the main adsorption mechanisms: hydrogen bonding, π -π interactions, anion-π interactions, and Lewis’ acid/base interactions.

Molecular simulation-based assessing of a novel metal-organic framework modified with alginate and chitosan biopolymers for anionic reactive black 5 and cationic crystal violet pollutants capture

This study employed molecular simulations to develop efficient and environmentally friendly adsorbents for removing two common dye pollutants, crystal violet (CRVT) and reactive black 5 (RBC5). The investigated adsorbents are based on biodegradable polymers alginate (ALG) and chitosan (CHAN) functionalized with carboxyl acid groups (CA) on a UIO-66 metal–organic framework (MOF). Density functional theory (DFT) analyses such as electrostatics potential (ESP), Average local ionization energy (ALIE) analysis, COSMO-RS (Conductor-like Screening Model for Real Solvents) analysis and the density of states (DOS) were performed to investigate the structures of the pollutants and adsorbents. Physical and chemical properties of the adsorbents, including density, Hamiltonian energy (HAE), the radius of gyration (ROG), and the stress autocorrelation function (SACF) were also examined. Additionally, molecular dynamics (MD) and Monte Carlo (MC) simulations were employed to study the adsorption of CRVT and RBC5 onto CA/UIO-66, CA/UIO-66/ALG, and CA/UIO-66/CHAN adsorbents. The results demonstrated that functionalizing CA/UIO-66 with CHAN and ALG significantly enhances the adsorption capacity for both CRVT and RBC5. The modified adsorbent demonstrated significantly higher affinity towards RBC5 compared to CRVT, as evidenced by the adsorption energies of −1.11 × 104 kcal/mol for CA/UIO-66-CHAN-W-CRVT and −1.36 × 107 kcal/mol for CA/UIO-66-CHAN-W-RBC5. This research highlights the potential of CHAN- and ALG-functionalized CA/UIO-66-based adsorbents as promising alternatives to current wastewater treatment methods. These adsorbents are efficient, biodegradable, and environmentally friendly, offering remarkable potential for removing dye pollutants from industrial and domestic wastewater.

Thiol-Amino Bifunctional Metal-Organic-Framework-Based Membrane Regulating Hydrophobic Sites for Selective Separation of Artesunate.

The selective separation and purification of artesunate (ARU) and artemisinin (ART) using zirconium-based metal-organic frameworks (MOF), especially UiO-66 MOF, are receiving increasing attention. In this study, tunable "hydrophobic" sites of thiol (-SH) were introduced to amino-functionalized MOFs (UiO-66-NH2) to fabricate a thiol-amino bifunctional UiO-66/polyvinylidene fluoride (PVDF)-blended membrane (S1-UiO/PVDF-DPIM) via the delayed-phase-inversion method for selective separation of ARU/ART. The adsorption results indicated that the modification of UiO-66-NH2 with thiol can indeed increase the ARU adsorption. The thiol-functional MOF (S1-UiO-66-NH2) was chosen as the optimal thiol-amino bifunctional MOF, as it possessed the maximum ARU adsorption capacity (111.14 mg g-1) and the highest selective-separation factor (α = 51.84). The ATR FT-IR dynamic spectrum disclosed the recognition mechanism, indicating that incorporating thiol groups into a hydrophilic MOF as hydrophobic sites can boost adsorption efficiency. Moreover, the static-selective permeation results showed that the S1-UiO/PVDF-DPIM preferentially transfers ARU when mixed with ART, even achieving complete ARU/ART separation. The most crucial aspect was the introduction of a hydrophobic core of -SH and new spontaneously formed disulfide bonds to S1-UiO/PVDF-DPIM, creating alternated hydrogen bonds and hydrophobic interactions. This work provides an alternative strategy to prepare hydrophobic-hydrophilic MOF-based membranes for the highly efficient and selective separation of complex analogue systems.

Collaborative adsorption and photocatalytic degradation of high concentration pharmaceutical pollutants in water using a novel dendritic fibrous nano-silica modified with chitosan and UiO-66

This study presents a novel hybrid mesoporous material for degrading drug pollutants in water. The hybrid materials, derived from UiO-66 metal-organic framework and chitosan, coated on nano-silica, showed excellent drug adsorption through hydrogen-bonding interactions and efficient photodegradation of antibiotics. The hybrid material's enhanced conductivity and reduced band gap significantly improved pollution reduction by minimising electron-hole recombination. This allows for more efficient charge transport and better light absorption, boosting the material's ability to break down pollutants. Structural and morphological analyses were conducted using various techniques, including scanning electron microscopy, X-ray diffraction, Fourier transform infrared spectroscopy, transmission electron microscopy, Brunauer-Emmett-Teller analysis, X-ray photoelectron spectroscopy, and thermogravimetric analysis. Optimising the adsorption-photodegradation process involved investigating pH, catalyst dose, and radiation time. Non-linear optimisation revealed an efficiency exceeding 85 % for 400 mg/L tetracycline and doxycycline, the model antibiotics. The optimal parameters for maximal elimination were determined as pH = 4.3, hybrid mesosphere dose = 4.0 mg/mL, and radiation time = 10 min. Kinetic studies favored pseudo-second-order diffusion models over pseudo-first-order models. The hybrid mesosphere showed sustained efficiency after three cycles and performed well in real aqueous samples, removing over 80 % of each antibiotic. This study demonstrates the potential of the hybrid mesoporous material for removing pharmaceutical pollutants in water systems.

Manipulating Ion Transport Regimes in Nanomembranes via a "Pore-in-Pore" Approach Enabled by the Synergy of Metal-Organic Frameworks and Solid-State Nanochannels.

Solid-state nanochannels (SSNs) have emerged as promising platforms for controlling ionic transport at the nanoscale. SSNs are highly versatile, and this feature can be enhanced through their combination with porous materials such as Metal-Organic Frameworks (MOF). By selection of specific building blocks and experimental conditions, different MOF architectures can be obtained, and this can influence the ionic transport properties through the nanochannel. Herein, we study the effects of confined synthesis of Zr-based UiO-66 MOF on the ion transport properties of single bullet-shaped poly(ethylene terephthalate) (PET) nanochannels. We have found that emerging textural properties from the MOF phase play a determinant role in controlling ionic transport through the nanochannel. We demonstrate that a transition from ion current saturation regimes to diode-like regimes can be obtained by employing different synthetic approaches, namely, counterdiffusion synthesis, where MOF precursors are kept separate and forced to diffuse through the nanochannel, and one-pot synthesis, where both precursors are placed at both ends of the channel. Also, by considering the dependence of the charge state of the UiO-66 MOF on the protonation degree, pH changes offered a mechanism to tune the iontronic output (and selectivity) among different regimes, including anion-driven rectification, cation-driven rectification, ion current saturation, and ohmic behavior. Furthermore, Poisson-Nernst-Planck (PNP) simulations were employed to rationalize the different iontronic outputs observed experimentally for membranes modified by different methods. Our results demonstrate a straightforward tool to synthesize MOF-based SSN membranes with tunable ion transport regimes.

Defect engineering of UiO-66 metal–organic framework: The role of temperature in the catalytic performance for methanol conversion

Defect engineering of UiO-66 metal–organic frameworks offers promising opportunities to develop catalytic applications. Recently, the methanol conversion reaction has been used to quantitatively investigate the catalytic properties of defective UiO-66. In this contribution, the role of synthesis temperature in creating structural defects of UiO-66 was evaluated. First, the catalysts were synthesized using the solvothermal method at various temperatures (100–220 °C). The XRD, SEM-PSD, FTIR, TG-DTG, BET, TPD-NH3, and TPD-CO2 techniques were used to study the characteristics. The findings suggested that raising the synthesis temperature enhanced the crystallinity, surface area, thermal stability, and acidity of catalysts. Following that, activity tests were performed at P = 101.3 kPa and T = 300–450 °C, and increasing the reaction temperature improved the catalyst’s performance. As a result, UiO-66 produced at 220 °C had the best performance (conversion = 51 %, yield DME = 81 %), and its activity remained stable at 450 °C for 6 h.

Assessing Activation Quality through Evaporative Drying Patterns of Zr-MOF (UiO-66) Colloidal Droplets.

We demonstrate a simple droplet diagnostic approach to monitor the UiO-66 MOF (metal-organic framework) synthesis and its quality using the sessile droplet drying phenomenon. Drying a sessile droplet involves evaporation-driven hydrodynamic flow and particle-nature-dependent self-assembled deposition. In general, the MOF synthesis process involves different sizes and physicochemical nature of particles in every synthesis stage. Equivalent quantities of each of purified pore-activated UiO-66 MOF, yet-to-be-purified pore-inactivated UiO-66 MOF, and reaction precursors of UiO-66 MOF give different deposition patterns when a well-dispersed aqueous droplet of these materials undergoes drying over substrates of varying stiffness and wettability. Yet-to-be-purified, pore-inactivated UiO-66 MOF nanoparticles undergo transport toward the droplet periphery, leading to a thick ring-like deposition at the dried droplet edge. Under appropriate drying conditions, such a deposit leads to desiccation-type mud-like reticular cracking. We study the origin of such ring-like deposits and cracks to understand how the surface charge density of UiO-66 particles controls their stability. We demonstrate that ZrOCl2 salt trapped in a nonpurified pore-inactivated UiO-66 MOF moiety is the principal reason for ring-like deposit formation and subsequent cracking in its dried aqueous droplet edge. Qualitatively, we identified Lewis acid salts that are capable of acting as Bro̷nsted acid upon hydrolysis (like FeCl3, SnCl2, and ZrOCl2), influence surface charge density and colloidal stability of dispersed UiO-66 MOF particles. As a result, immediate particle coagulation is avoided, so those travel to the droplet edge, forming ring-like deposition and subsequent cracking upon drying. Further, we show that crack patterns on such deposits are highly dependent on the stiffness and temperature of depositing substrates via a competition between axial and lateral strains at the deposit-substrate interface.

Catalytic transfer hydrogenation of α-angelica lactone over Nickel(II) modified UiO-66 metal organic framework under mild conditions

In the realm of biomass valorization, catalysts play a pivotal role, and UiO-66(Zr), a type of metal organic framework (MOF), emerges as a promising heterogeneous catalyst. This study focuses on incorporating Ni2+ into UiO-66(Zr) for application in catalytic transfer hydrogenation (CTH) of bio-derived α-angelica lactone (a-AL) to ɣ-valerolactone (GVL). The synthesis of UiO-66(Zr) occurs through a solvothermal process at 120 °C for 24 h. Ni(II) modification, achieved through wet impregnation with loadings of 2.5 and 5.0 wt%, results in no observable diffraction peaks associated with Ni particles in XRD analysis. FTIR analysis indicates significant shifts, suggesting deprotonation of the carboxylic moiety from the ligand and coordination with Zr4+ metal ion. Nitrogen sorption isotherms show a reduction in surface area and pore volume upon Ni(II) incorporation. FESEM analysis reveals particle agglomeration and increased size with Ni(II) introduction. EDX and HRTEM confirm the presence of 0.9 and 1.8 wt% Ni(II) on UiO-66(Zr). TG/DTA analysis affirms that Ni(II) does not affect the thermal stability of UiO-66(Zr). Ultimately, the introduction of Ni(II) enhances the catalytic performance of UiO-66(Zr), increasing the conversion and selectivity towards ɣ-valerolactone from 67 to 83.3 % and 71.6 % to 97.4 %, respectively, under mild reaction conditions.

Deep Oxidative Desulfurization of Planar Compounds Over Functionalized Metal–Organic Framework UiO-66(Zr): An Optimization Study

Deep Oxidative Desulfurization of Planar Compounds Over Functionalized Metal–Organic Framework UiO-66(Zr): An Optimization Study

Triflate-Functionalized UiO-66 Metal–Organic Framework Nanoparticles for Tandem Synthesis of Xanthones

Triflate-Functionalized UiO-66 Metal–Organic Framework Nanoparticles for Tandem Synthesis of Xanthones

Amino-Functionalizing Ce-Based MOF UiO-66 for Enhanced CO2 Adsorption and Selectivity.

Metal-organic frameworks (MOF) hold great promise for CO2 adsorption due to their high surface areas, tunable pore sizes, and the ability to modify their chemical properties to enhance CO2 affinity. MOFs tagged with functional groups either at linker or metal sites have shown improved CO2 uptake capacity and selectivity. This study focuses on investigating the potential of selective CO2 adsorption using amino functionalization of linker forming Ce-UiO-66. The physicochemical properties and characteristics of MOFs to determine the degree of amino functionalization and structural stability were examined using powder X-ray diffraction (PXRD), Fourier transformer infra-red (FTIR), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), and N2 porosimetry and specific surface area (BET). This work unveils a novel array of results on CO2, N2 and water vapour adsorption on Ce-UiO-66-NH2. The amino-functionalized Ce-UiO-66-NH2 shows 63 % higher CO2 uptake and 84 % higher CO2/N2 selectivity at 273 K and 1 bar over Ce-UiO-66. Ce-UiO-66-NH2 also shows excellent structural stability after gas and vapour sorption making Ce-UiO-66-NH2 potential adsorbent for CO2 capture.

UiO-66(Zr) as drug delivery system for non-steroidal anti-inflammatory drugs

The toxicity for the human body of non-steroidal anti-inflammatory drugs (NSAIDs) overdoses is a consequence of their low water solubility, high doses, and facile accessibility to the population. New drug delivery systems (DDS) are necessary to overcome the bioavailability and toxicity related to NSAIDs. In this context, UiO-66(Zr) metal-organic framework (MOF) shows high porosity, stability, and load capacity, thus being a promising DDS. However, the adsorption and release capability for different NSAIDs is scarcely described. In this work, the biocompatible UiO-66(Zr) MOF was used to study the adsorption and release conditions of ibuprofen, naproxen, and diclofenac using a theoretical and experimental approximation. DFT results showed that the MOF-drug interaction was due to an intermolecular hydrogen bond between protons of the groups in the defect sites, (μ3 − OH, and − OH2) and a lone pair of oxygen carboxyl functional group of the NSAIDs. Also, the experimental results suggest that the solvent where the drug is dissolved affects the adsorption process. The adsorption kinetics are similar between the drugs, but the maximum load capacity differs for each drug. The release kinetics assay showed a solvent dependence kinetics whose maximum liberation capacity is affected by the interaction between the drug and the material. Finally, the biological assays show that none of the systems studied are cytotoxic for HMVEC. Additionally, the wound healing assay suggests that the UiO-66(Zr) material has potential application on the wound healing process. However, further studies should be done.

Highly dispersed active sites and strong metal-support interaction for boosting CO2 hydrogenation to methanol

As global energy demand continues to increase and global climate change issues caused by greenhouse gas emissions gradually heat up, the effective conversion of carbon dioxide into high value-added methanol has become a key challenge in the energy and environmental fields. However, due to the chemical inertness of CO2 molecules, it is difficult to activate CO2 at low temperatures, resulting in extremely low conversion rates. Although increasing the reaction temperature is beneficial for the conversion of CO2, there is also competition in the reverse water gas reaction, resulting in lower methanol selectivity. Therefore, developing efficient catalysts is the key to improving CO2 conversion rate and methanol selectivity. In this work, we used zirconium-based UIO-66 metal-organic framework as a precursor, replaced the original terephthalic acid ligand with thermally unstable aminoterephthalic acid, and supported Cu on the MOF precursor by equal volume impregnation method. After heat treatment, the Cu/ZrO2-DM catalyst was prepared. The catalyst was compared with Cu/ZrO2 catalyst prepared by co-precipitation method, hydrothermal method and unmodified Cu/ZrO2-D catalyst. The Cu/ZrO2-DM catalyst exhibited the highest CO2 conversion and methanol selectivity in the hydrogenation reaction, reaching 13.95% and 90.78%, respectively. The main reason is attributed to the large specific surface area of the copper-based catalyst derived from MOF materials, the good dispersion of the active center and the strong interaction between Cu and the precursor. This work may provide a new perspective for the design and synthesis of related catalytic materials for efficient CO2 hydrogenation to methanol.

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.

A facile and efficient voltammetric sensor for marbofloxacin detection based on zirconium-based metal-organic framework UiO-66/nitrogen-doped graphene nanocomposite

Improper and persistent use of marbofloxacin (MAR) is prone to produce residues that deteriorate the surrounding environment and endanger our health. Hence, it is urgent to stablish a facile and efficient detection technique for the detection of MAR. Herein, a highly efficient electrochemical platform was constructed for sensitive determination of MAR using zirconium-based metal–organic framework (UiO-66)/nitrogen-doped graphene (NG) nanocomposites (UiO-66/NG). The surface morphology, crystalline phase, elemental composition, and electrochemical behavior of UiO-66/NG were characterized by various spectroscopic and electrochemical techniques. Owing to the synergistic interaction of UiO-66 MOFs and NG nanosheets, the UiO-66/NG exhibited remarkable catalytic activity for MAR oxidation. As consequently, the UiO-66/NG demonstrated a wide linear response range (0.01 − 10 μM), high sensitivity (1.80 μM μA−1 cm−2) and low detection limit (0.002 μM). The proposed UiO-66/NG/GCE demonstrated robust voltammetric responses even in the presence of excess potential interfering species and retained stable response signals for at least two weeks. More importantly, the proposed UiO-66/NG/GCE displayed highly consistent sensitivity toward MAR detection in both aquaculture water and milk matrices and PBS buffer, and achieved accurate and sensitive detection of MAR with good recovery. Together with its low cost and facile operation, the UiO-66/NG/GCE shows great prospects for trace detection of MAR from complex matrices.