Novel aspartic-based bio-MOF adsorbent for effective anionic dye decontamination from polluted water.

In this study, a cost-effective powdered Zn l-aspartic acid bio-metal organic framework (Zn l-Asp bio-MOF) was reported as an efficient adsorbent for Direct Red 81 (DR-81) as an anionic organic dye. The prepared bio-MOF was characterized using Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM), field emission transmission electron microscopy (FETEM), surface area analysis (BET), and thermal gravimetrical analysis (TGA). The resulting bio-MOF has a large surface area (180.43 m2 g-1) and large mesopore volume (0.144 cm3 g-1), as well as good chemical inertness and mechanical stability. The optimum dosage from the Zn l-Asp bio-MOF was 1.0 g L-1 at pH = 7 for 95.3% adsorption of 10 ppm DR-81 after 45 min. Thermodynamic analysis results demonstrated that the decontamination processes were done with spontaneous, thermodynamically, and exothermic nature onto the fabricated bio-MOF. Kinetic parameters were well-fitted with pseudo-second-order kinetics, and the adsorption process was described by the Freundlich isotherm. The adsorption data proved that Zn l-Asp bio-MOF is an effective adsorbent for DR-81 from aqueous solutions with high stability and recycling ability for eight cycles, as well as the easy regeneration of the sorbent.

Bio-Zirconium Metal-Organic Framework Regenerable Bio-Beads for the Effective Removal of Organophosphates from Polluted Water.

Organophosphate-based pesticides, such as diazinon, are among the most toxic organic contaminants to human and environment. Effective removal of diazinon from contaminated water sources is critical. Zirconium Metal-organic frameworks (Zr-MOFs) are promising candidates for the removal of organic contaminants from wastewater. Herein, we report the adequacy of a bio based Zr-MOF named MIP-202 for the removal of diazinon from water. On the other hand, the use of these materials in powder form is not workable, the development of scalable and economical processes and integrative of these materials onto beads is paramount for industrial processes. Hence, it was reported a scalable, bio aqueous solution-based preparation strategy for Bio Zr-MOF beads production. The composite material exposed identical reactivity under the same ambient parameters compared to powdered material in an aqueous solution. These results signify a critical procedure to an integrated strategy for organophosphates removal using bio-based MOFs, which demonstrates high potential for manufacturing applications such as continued removal of organophosphates from wastewater supplies.

Photocatalytic Degradation of Malachite Green Dye from Aqueous Solution Using Environmentally Compatible Ag/ZnO Polymeric Nanofibers.

An efficient, environmentally compatible and highly porous, silver surface-modified photocatalytic zinc oxide/cellulose acetate/ polypyrrole ZnO/CA/Ppy hybrid nanofibers matrix was fabricated using an electrospinning technique. Electrospinning parameters such as solution flow rate, applied voltage and the distance between needles to collector were optimized. The optimum homogenous and uniform ZnO/CA/Ppy polymeric composite nanofiber was fabricated through the dispersion of 0.05% wt ZnO into the dissolved hybrid polymeric solution with an average nanofiber diameter ranged between 125 and 170 nm. The fabricated ZnO-polymeric nanofiber was further surface-immobilized with silver nanoparticles to enhance its photocatalytic activity through the reduction of the nanofiber bandgap. A comparative study between ZnO polymeric nanofiber before and after silver immobilization was investigated using X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscopy (TEM), Fourier transform infrared (FTIR) and thermal gravimetric analysis (TGA). The photocatalytic degradation efficiency of the two different prepared nanofibers before and after nanosilver immobilization for malachite green (MG) dye was compared against various experimental parameters. The optimum degradation efficiency of nanosilver surface-modified ZnO-polymeric nanofibers was recorded as 93.5% for malachite green dye after 1 h compared with 63% for ZnO-polymeric nanofibers.

Biocompatible MIP-202 Zr-MOF tunable sorbent for cost-effective decontamination of anionic and cationic pollutants from waste solutions.

This reported work aims to fabricate an eco-friendly Zr bio-based MOF and assessment its adsorption efficiency towards the cationic and anionic dye pollutants including methylene blue (MB) and direct red 81 (DR-81), respectively. Also, its adsorption tendency for the highly toxic heavy metal of hexavalent chromium (Cr(VI)) was compared with dyes. The adsorption performance of bio-MOF showed that the maximum monolayer adsorption capacities were recorded as 79.799 mg/g for MB, 36.071 mg/g for DR-81, and 19.012 mg/g for Cr(VI). Meanwhile, the optimum dosage of as-synthesized MIP-202 bio-MOF was 0.5, 1, and 2 g L-1 for MB, DR-81, and Cr(VI), respectively. Thermodynamic analysis demonstrated the spontaneous, thermodynamically, and endothermic nature of the decontamination processes onto the fabricated Zr bio-based MOF. The adsorption data were fitted by Langmuir isotherm model compared with Freundlich and Temkin models for all studied water pollutants. Pseudo-second-order kinetic model was a fit model for description of the adsorption kinetics of the different cationic and anionic pollutants onto Zr bio-based MOF. These outcomes indicated that Zr bio-based MOF has potential application for adsorption of different types of industrial water pollutants including cationic and anionic dyes and heavy metals.

Novel Magnetic Zinc Oxide Nanotubes for Phenol Adsorption: Mechanism Modeling.

Considering the great impact of a material's surface area on adsorption processes, hollow nanotube magnetic zinc oxide with a favorable surface area of 78.39 m²/g was fabricated with the assistance of microwave technology in the presence of poly vinyl alcohol (PVA) as a stabilizing agent followed by sonic precipitation of magnetite nano-particles. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) micrographs identified the nanotubes' morphology in the synthesized material with an average aspect ratio of 3. X-ray diffraction (XRD) analysis verified the combination of magnetite material with the hexagonal wurtzite structure of ZnO in the prepared material. The immobilization of magnetite nanoparticles on to ZnO was confirmed using vibrating sample magnetometry (VSM). The sorption affinity of the synthesized magnetic ZnO nanotube for phenolic compounds from aqueous solutions was examined as a function of various processing factors. The degree of acidity of the phenolic solution has great influence on the phenol sorption process on to magnetic ZnO. The calculated value of ΔH° designated the endothermic nature of the phenol uptake process on to the magnetic ZnO nanotubes. Mathematical modeling indicated a combination of physical and chemical adsorption mechanisms of phenolic compounds on to the fabricated magnetic ZnO nanotubes. The kinetic process correlated better with the second-order rate model compared to the first-order rate model. This result indicates the predominance of the chemical adsorption process of phenol on to magnetic ZnO nanotubes.

Adsorption Profile of Basic Dye onto Novel Fabricated Carboxylated Functionalized Co-Polymer Nanofibers.

Acrylonitrile-Styrene co-polymer was prepared by solution polymerization and fabricated into nanofibers using the electrospinning technique. The nanofiber polarization was enhanced through its surface functionalization with carboxylic acid groups by simple chemical modification. The carboxylic groups' presence was dedicated using the FT-IR technique. SEM showed that the nanofiber attains a uniform and porous structure. The equilibrium and kinetic behaviors of basic violet 14 dye sorption onto the nanofibers were examined. Both Langmuir and Temkin models are capable of expressing the dye sorption process at equilibrium. The intraparticle diffusion and Boyd kinetic models specified that the intraparticle diffusion step was the main decolorization rate controlling the process.

Immobilization of Magnetic Nanoparticles onto Amine-Modified Nano-Silica Gel for Copper Ions Remediation.

A novel nano-hybrid was synthesized through immobilization of amine-functionalized silica gel nanoparticles with nanomagnetite via a co-precipitation technique. The parameters, such as reagent concentrations, reaction temperature and time, were optimized to accomplish the nano-silica gel chelating matrix. The most proper amine-modified silica gel nanoparticles were immobilized with magnetic nanoparticles. The synthesized magnetic amine nano-silica gel (MANSG) was established and characterized using X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), Fourier transform infrared (FTIR), thermal gravimetric analysis (TGA), differential scanning calorimetry (DSC) and vibrating sample magnetometry (VSM). The feasibility of MANSG for copper ions' remediation from wastewater was examined. MANSG achieves a 98% copper decontamination from polluted water within 90 min. Equilibrium sorption of copper ions onto MANSG nanoparticles obeyed the Langmuir equation compared to the Freundlich, Temkin, Elovich and Dubinin-Radushkevich (D-R) equilibrium isotherm models. The pseudo-second-order rate kinetics is appropriate to describe the copper sorption process onto the fabricated MANSG.