scholarly journals Study of the adsorption of an organic pollutant onto a microporous metal organic framework

2020 ◽  
Author(s):  
Mansouri Taki Eddine Mohammed ◽  
Nibou Djamel ◽  
Trari Mohamed ◽  
Samira Amokrane
Keyword(s):  
Methyl Orange ◽  
Adsorption Capacity ◽  
Active Sites ◽  
Physical Adsorption ◽  
Metal Organic Framework ◽  
Specific Interaction ◽  
Maximum Adsorption Capacity ◽  
Film Diffusion ◽  
Metal Organic ◽  
Organic Framework

Abstract In this study, the microporous Metal Organic Framework-5 (MOF-5) has been synthesized to be used to remove methyl orange by adsorption. The adsorption experiments exhibit a good adsorption capacity at a catalyst dose of 0.1 g L−1 and for an initial concentration of 200 mg L−1, whereas the performance is stable over a wide pH range. The equilibrium adsorption data showed a sigmoidal course, which is well fitted by the Dubinin-Astakhov model applicable for physical adsorption processes (E = 0.055 kJ mol−1) onto heterogeneous surfaces and a more homogeneous pore structure (n = 9.9), with a maximum adsorption capacity of 1248.35 mg g−1. As can be observed from the evaluation of the kinetic data, the surface of the adsorbent is heterogeneous with different active sites for Methyl Orange (MO) adsorption. Moreover, based on the rate constant, it can be suggested that there is a specific interaction like electrostatic interaction between MO and the adsorbent for rapid and high uptake of the dye, whereas the adsorption phenomenon is reversible. According to the adsorption mechanisms, intra-particle and film diffusion models simultaneously controlled the rate sorption, which was confirmed by the calculated intra-particle diffusion and the film diffusion coefficients. The evaluation of the thermodynamic parameters revealed that the MO adsorption is spontaneous, endothermic and the randomness increases with the adsorption of MO.

scholarly journals Synergistic effect of carboxyl and sulfate groups for effective removal of radioactive strontium ion in a Zr-metal-organic framework

2021 ◽  
Author(s):  
Lin Ren ◽  
Xudong Zhao ◽  
Baosheng Liu ◽  
Hongliang Huang
Keyword(s):  
Adsorption Capacity ◽  
High Efficiency ◽  
Metal Organic Framework ◽  
Maximum Adsorption Capacity ◽  
Potential Candidate ◽  
Dual Groups ◽  
Metal Organic ◽  
Strontium Ion ◽  
Rapid Adsorption ◽  
Organic Framework

Abstract Rapid removal of radioactive strontium from nuclear wastewater is of great significance for environment safety and human health. This work reported the effective adsorption of strontium ion in a stable dual-group metal-organic framework, Zr6(OH)14(BDC-(COOH)2)4(SO4)0.75 (Zr-BDC-COOH-SO4), which contains strontium-chelating groups (-COOH and SO4) and strongly ionizable group (-COOH). Zr-BDC-COOH-SO4 exhibits very rapid adsorption kinetics (<5 min) and a maximum adsorption capacity of 67.5 mg g−1. The adsorption behaviors can be well evaluated by pseudo-second-order model and Langmuir isotherm model. Further investigations indicate that the adsorption of Sr2+ in Zr-BDC-COOH-SO4 would not be interfered by solution pH and adsorption temperature obviously. Feasible regeneration of the adsorbent was also demonstrated through a simple elution method. Mechanism investigation suggests that free -COOH contributes to the rapid adsorption based on electrostatic interaction while introduction of -SO4 can enhance the adsorption capacity largely. Thus, these results suggest that Zr-BDC-COOH-SO4 might be a potential candidate for Sr2+ removal and introducing dual groups is an effective strategy for designing high-efficiency adsorbents.

scholarly journals Experimental and Modeling of Dicamba Adsorption in Aqueous Medium Using MIL-101(Cr) Metal-Organic Framework

Processes ◽  
2021 ◽  
Vol 9 (3) ◽  
pp. 419
Author(s):  
Hamza Ahmad Isiyaka ◽  
Khairulazhar Jumbri ◽  
Nonni Soraya Sambudi ◽  
Jun Wei Lim ◽  
Bahruddin Saad ◽  
...  
Keyword(s):  
Aqueous Medium ◽  
Adsorption Capacity ◽  
Environmental Concern ◽  
Metal Organic Framework ◽  
High Surface ◽  
High Surface Area ◽  
Data Matrix ◽  
Adsorption Parameters ◽  
Metal Organic ◽  
Organic Framework

Drift deposition of emerging and carcinogenic contaminant dicamba (3,6-dichloro-2-methoxy benzoic acid) has become a major health and environmental concern. Effective removal of dicamba in aqueous medium becomes imperative. This study investigates the adsorption of a promising adsorbent, MIL-101(Cr) metal-organic framework (MOF), for the removal of dicamba in aqueous solution. The adsorbent was hydrothermally synthesized and characterized using N2 adsorption-desorption isotherms, Brunauer, Emmett and Teller (BET), powdered X-ray diffraction (XRD), Fourier Transformed Infrared (FTIR) and field emission scanning electron microscopy (FESEM). Adsorption models such as kinetics, isotherms and thermodynamics were studied to understand details of the adsorption process. The significance and optimization of the data matrix, as well as the multivariate interaction of the adsorption parameters, were determined using response surface methodology (RSM). RSM and artificial neural network (ANN) were used to predict the adsorption capacity. In each of the experimental adsorption conditions used, the ANN gave a better prediction with minimal error than the RSM model. The MIL-101(Cr) adsorbent was recycled six times to determine the possibility of reuse. The results show that MIL-101(Cr) is a very promising adsorbent, in particular due to the high surface area (1439 m2 g−1), rapid equilibration (~25 min), high adsorption capacity (237.384 mg g−1) and high removal efficiency of 99.432%.

Atomic regulation of metal-organic framework derived carbon-based single-atom catalysts for electrochemical CO2 reduction reaction

2021 ◽  
Author(s):  
Danni Zhou ◽  
Xinyuan Li ◽  
Huishan Shang ◽  
Fengjuan Qin ◽  
Wenxing Chen
Keyword(s):  
Active Sites ◽  
Metal Organic Framework ◽  
Co2 Reduction ◽  
Carbon Dioxide Reduction ◽  
Reduction Reaction ◽  
Single Atom ◽  
Electrochemical Co2 Reduction ◽  
Metal Organic ◽  
Co2 Reduction Reaction ◽  
Organic Framework

Metal-organic framework (MOF) derived single-atom catalysts (SACs), featured unique active sites and adjustable topological structures, exhibit high electrocatalytic performance on carbon dioxide reduction reactions (CO2RR). By modulating elements and atomic...

Highly selective CO2 separation from a CO2/C2H2 mixture using a diamine-appended metal–organic framework

2021 ◽  
Vol 9 (37) ◽  
pp. 21424-21428
Author(s):  
Doo San Choi ◽  
Dae Won Kim ◽  
Dong Won Kang ◽  
Minjung Kang ◽  
Yun Seok Chae ◽  
...  
Keyword(s):  
Adsorption Capacity ◽  
Metal Organic Framework ◽  
Co2 Separation ◽  
Metal Organic ◽  
Organic Framework

A diamine-appended metal–organic framework displays a top-tier CO2/C2H2 selectivity, a record-high CO2 adsorption capacity, and recyclability.

scholarly journals Photocatalytic Degradation of Methylene Blue and Methyl Orange by Y-PTC Metal-Organic Framework

2021 ◽  
Vol 7 (2) ◽  
pp. 129-141
Author(s):  
Adawiah Adawiah ◽  
Muhammad Derry Luthfi Yudhi ◽  
Agustino Zulys
Keyword(s):  
Methylene Blue ◽  
Photocatalytic Activity ◽  
Methyl Orange ◽  
Visible Light ◽  
Visible Light Irradiation ◽  
Metal Organic Framework ◽  
Light Irradiation ◽  
Bandgap Energy ◽  
Metal Organic ◽  
Organic Framework

The yttrium based metal-organic framework (MOF) Y-PTC was synthesized by the solvothermal method using perylene as the linker and yttrium as metal ion. This study aims to assess the photocatalytic activity of yttrium-perylenetetracarboxylate (Y-PTC) metal-organic framework (MOF) toward methylene blue and methyl orange under visible light irradiation. The results of the FTIR analysis showed that Y-PTC MOF had a different structure and composition from its precursor (Na4PTC). The Y-PTC MOF has a bandgap energy value of 2.20 eV with a surface area of 47.7487 m2/g. The SEM-EDS analysis showed an elemental composition of yttrium, carbon, and oxygen, were 6.9%, 72.1% and 20.7%, respectively. Furthermore, Y-PTC MOF was able to adsorb dyes at the optimum by 78.10% and 35.57% toward methylene blue (MB) and methyl orange (MO) at the dispersion period of 60 mins. Y-PTC MOF exhibited photocatalytic activity towards the degradation of methylene blue and methyl orange under visible light irradiation. The addition of H2O2 inhibited Y-PTC photocatalytic activity towards MO degradation from 50.89% to 26.38%. In contrast to MO, the addition of H2O2 had a positive effect on MB, which increased the degradation from 87.56% to 91.65%. Therefore, Y-PTC MOF possessed the potential of a photocatalyst material in dyes degradation under visible light irradiation.

scholarly journals A Zirconium Metal-Organic Framework with SOC Topological Net for Catalytic Peptide Bond Hydrolysis

2021 ◽  
Author(s):  
Sujing Wang ◽  
Antoine Tissot ◽  
Guillaume Maurin ◽  
Tatjana Parac-Vogt ◽  
Christian Serre ◽  
...  
Keyword(s):  
Active Sites ◽  
Metal Organic Framework ◽  
Cost Effective ◽  
Peptide Bond ◽  
Catalytic Performance ◽  
Wide Range ◽  
Horse Heart Myoglobin ◽  
Metal Organic ◽  
Effective Synthesis ◽  
Organic Framework

<div>The discovery of nanozymes for selective cleavage of proteins would boost the emerging areas of modern proteomics, however, the development of efficient and reusable artificial catalysts for peptide bond hydrolysis is challenging. Here we report the detailed catalytic properties of a microporous zirconium carboxylate metal-organic framework, MIP-201, in promoting peptide bond hydrolysis in a simple dipeptide, as well as in horse-heart myoglobin (Mb) protein that consists of 153 amino acids. We demonstrate that MIP-201 features an excellent catalytic activity and selectivity, a good tolerance toward reaction conditions covering a wide range of different pH values, and importantly, an exceptional recycling ability associated with easy regeneration process. Taking into account the excellent catalytic performance of MIP-201 and its other advantages such as 6-connected Zr6 cluster active sites, the green, scalable and cost-effective synthesis, and an outstanding chemical and architectural stability, our finding suggests that MIP-201 may be a promising and practical alternative to the current commercially available catalysts for peptide bond hydrolysis.</div>

scholarly journals A Zirconium Metal-Organic Framework with SOC Topological Net for Catalytic Peptide Bond Hydrolysis

2021 ◽  
Author(s):  
Sujing Wang ◽  
Antoine Tissot ◽  
Guillaume Maurin ◽  
Tatjana Parac-Vogt ◽  
Christian Serre ◽  
...  
Keyword(s):  
Active Sites ◽  
Metal Organic Framework ◽  
Cost Effective ◽  
Peptide Bond ◽  
Catalytic Performance ◽  
Wide Range ◽  
Horse Heart Myoglobin ◽  
Metal Organic ◽  
Effective Synthesis ◽  
Organic Framework

<div>The discovery of nanozymes for selective cleavage of proteins would boost the emerging areas of modern proteomics, however, the development of efficient and reusable artificial catalysts for peptide bond hydrolysis is challenging. Here we report the detailed catalytic properties of a microporous zirconium carboxylate metal-organic framework, MIP-201, in promoting peptide bond hydrolysis in a simple dipeptide, as well as in horse-heart myoglobin (Mb) protein that consists of 153 amino acids. We demonstrate that MIP-201 features an excellent catalytic activity and selectivity, a good tolerance toward reaction conditions covering a wide range of different pH values, and importantly, an exceptional recycling ability associated with easy regeneration process. Taking into account the excellent catalytic performance of MIP-201 and its other advantages such as 6-connected Zr6 cluster active sites, the green, scalable and cost-effective synthesis, and an outstanding chemical and architectural stability, our finding suggests that MIP-201 may be a promising and practical alternative to the current commercially available catalysts for peptide bond hydrolysis.</div>

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