ZIF-8 metal organic framework materials as a superb platform for the removal and photocatalytic degradation of organic pollutants: a review.

Metal organic frameworks (MOFs) are attracting significant attention for applications including adsorption, chemical sensing, gas separation, photocatalysis, electrocatalysis and catalysis. In particular, zeolitic imidazolate framework 8 (ZIF-8), which is composed of zinc ions and imidazolate ligands, have been applied in different areas of catalysis due to its outstanding structural and textural properties. It possesses a highly porous structure and chemical and thermal stability under varying reaction conditions. When used alone in the reaction medium, the ZIF-8 particles tend to agglomerate, which inhibits their removal efficiency and selectivity. This results in their mediocre reusability and separation from aqueous conditions. Thus, to overcome these drawbacks, several well-designed ZIF-8 structures have emerged by forming composites and heterostructures and doping. This review focuses on the recent advances on the use of ZIF-8 structures (doping, composites, heterostructures, etc.) in the removal and photodegradation of persistent organic pollutants. We focus on the adsorption and photocatalysis of three main organic pollutants (methylene blue, rhodamine B, and malachite green). Finally, the key challenges, prospects and future directions are outlined to give insights into game-changing breakthroughs in this area.

ZIF-8 metal organic framework composites as hydrogen evolution reaction photocatalyst: A review of the current state.

In the past decade, extensive research has been devoted to synthesis of ZIF-8 materials for catalytic applications. As physico-chemical properties are synthesis-dependent, this review explores different synthesis strategies based the solvent and solvent-free synthesis of zeolitic imidazole framework. Accordingly, the effect of several parameters on the ZIF-8 synthesis were discussed including solvent, deprotonating agents, precursors ratio is delivered. Additionally, the advantages and disadvantages of each synthesis have been discussed and assessed. ZIF-8 textural and structural properties justify its wide use as a stable high surface area MOF in aqueous catalytic reactions. This review includes the applicatios of ZIF-8 materials in photocatalytic hydrogen evolution reaction (HER). The efficiency of the reviewed materials was fairly assessed. Finally, Limitations, drawbacks and future challenges were fully debated to ensure the industrial viability of the ZIFs.

Selected pharmaceuticals removal using algae derived porous carbon: experimental, modeling and DFT theoretical insights.

Porous carbon from Laminaria digitata algae activated using NaOH (PCLD@NaOH) was prepared by a chemical activation approach and has been tested for the adsorption of ketoprofen and aspirin molecules. The prepared PCLD@NaOH was characterized using XPS, FTIR, Raman, N2-physisorption, SEM, acidic/basic character (Boehm), and pHPZC. The batch adsorption of ketoprofen and aspirin was investigated under different parameters. The adsorption kinetics on PCLD@NaOH were well described by the Avrami-fractional kinetic model and the equilibrium data by Liu isotherm model. The adsorption capacity of aspirin (970.88 mg g-1 at 25 °C) was higher than ketoprofen (443.45 mg g-1 at 25 °C). The thermodynamic values indicate that the adsorption of ketoprofen and aspirin is exothermic and spontaneous. These results were in good agreement with DFT calculation that shows that the aspirin molecule presents high reactivity, electrophilicity, and softness compared to the ketoprofen molecule. Finally, the response surface methodology was used to optimize the removal efficiency of ketoprofen and aspirin.

Acridine orange adsorption by zinc oxide/almond shell activated carbon composite: Operational factors, mechanism and performance optimization using central composite design and surface modeling.

Zinc Oxide/Activated Carbon Powder was used for the adsorptive removal of Acridine Orange dye (AO) from aqueous solution. The prepared composite material was characterized using XRD, XPS, SEM, EDS, FTIR, XRF, Raman, BET surface area and TGA/DTA. The adsorption isotherms, kinetics and thermodynamic studies of AO onto the ZnO-AC were thoroughly analyzed. The kinetic modeling data revealed that the adsorption of AO has a good adjustment to the pseudo-second-order model. Langmuir isotherm model is better fitted for adsorption data and the maximum adsorption capacity was found to be 909.1 mg/g at 313 K. The negative values of ΔG showed the spontaneous nature of the AO adsorption onto ZnO-AC. The results indicated the adsorption was pH dependent which is mainly governed by electrostatic attraction, hydrogen bonding and π-π interaction. Reusability test showed a low decrease in the removal performance of ZnO-AC due to the mesopore filling mechanism confirmed by BET analysis after adsorption. Also, thermal regeneration could deposit AO dye on the surface of the composite leading to the efficiency decrease. Finally, the effect of various parameters such as pH, temperature, contact time and initial dye concentration was studied using response surface methodology (RSM). The model predicted a maximum AO removal (99.42 ± 0.57%) under the optimum conditions, which was very close to the experimental value (99.32 ± 0.18%).