Design, preparation, and performance of different adsorbents based on carboxymethyl chitosan/sodium alginate hydrogel beads for selective adsorption of Cadmium (II) and Chromium (III) metal ions.

Developing cost-effective and efficient adsorbents for heavy metals in multicomponent systems is a challenge that needs to be resolved to meet the challenges of wastewater treatment technology. Two adsorbents were synthesized, characterized, and investigated for the removal of Cd2+ and Cr3+ as model heavy metals in their single and binary solutions. The first adsorbent (ACZ) was a nanocomposite formed of O-Carboxymethyl chitosan, sodium alginate, and zeolite. While, the other (ACL) contained ZnFe layered double hydroxides instead of the zeolite phase. Adsorbents were characterized using XRD, FTIR, SEM, and swelling degree analysis. For single heavy metal adsorption isotherms, data for both adsorbents was best fitted and indicated a multilayer adsorption nature. For binary adsorption, Langmuir model with interacting parameters showed the best results compared to other models for both pollutants. For single system, Avrami model was found to be the best model representing the adsorption kinetics data, which indicates that the mechanism of adsorption follows multiple kinetic orders that may change during duration of adsorption process. Numerous interaction mechanisms can occur between the heavy metals and functional groups in the synthesized hydrogels such as NH2, COOH, and OH groups leading to efficient adsorption of metal ions.

Antifungal and antibacterial investigation of quinary Zr Al Fe Co Ni layered double hydroxide and its Al Fe Co Ni quaternary and Fe Co Ni tertiary roots.

Layered double hydroxides (LDH) are promising 2D nanomaterials being investigated for several engineering and biomedical applications. In this work, quinary Zr Al Fe Co Ni LDH and its Al Fe Co Ni LDH quaternary and Fe Co Ni LDH tertiary roots were prepared and characterized. All samples showed an aggregated, layered morphology with zero surface charge and approximately 300 nm of hydrodynamic size. BET surface area of Al Fe Co Ni LDH showed a remarkable value of 143.25 m2 g-1 as opposed to 26.2 m2 g-1 and 45.4 m2 g-1 for Fe Co Ni LDH and Zr Al Fe Co Ni LDH, respectively. The antimicrobial activity of the prepared samples was assessed against the many pathogenic bacteria; Bacillus (B.) subtilis, Escherichia (E.) coli, Haemophilus (H.) influenza, Listeria (L.) monocytogenes, Staphylococcus (S.) aureus, and Streptococcus (St.) pneumonia, and six fungal species. Furthermore, anti-biofilm activity, growth curve assay, and effect of UV illumination were examined against various pathogenic microbes. Zr Al Fe Co Ni displayed remarkable antibacterial activity, as indicated by the lowest values of the minimum inhibitory concentrations (MIC) of 4-166.7 µg mL-1. Results for fungal strains varied in terms of their susceptibilities for the different samples tested. Zn Al Fe Co Ni was able to inhibit the biofilm formation of S. aureus (96.09%), E. coli (98.32%), and Candida (C.) albicans (95.93%). This study shown that certain LDH categories, particularly Zr Al Fe Co Ni, may be promising antibacterial agents against variety of pathogenic microorganisms that cause serious infections.

Expression of concern: Acceleration of ammonium phosphate hydrolysis using TiO2 microspheres as a catalyst for hydrogen production.

Expression of concern for 'Acceleration of ammonium phosphate hydrolysis using TiO2 microspheres as a catalyst for hydrogen production' by Ayman H. Zaki et al., Nanoscale Adv., 2020, 2, 2080-2086, https://doi.org/10.1039/D0NA00204F.

Investigation of ternary Zn-Co-Fe layered double hydroxide as a multifunctional 2D layered adsorbent for moxifloxacin and antifungal disinfection.

Layered double hydroxides have recently gained wide interest as promising multifunctional nanomaterials. In this work, a multifunctional ternary Zn-Co-Fe LDH was prepared and characterized using XRD, FTIR, BET, TEM, SEM, and EDX. This LDH showed a typical XRD pattern with a crystallite size of 3.52 nm and a BET surface area of 155.9 m2/g. This LDH was investigated, for the first time, as an adsorbent for moxifloxacin, a common fluoroquinolones antibiotic, showing a maximum removal efficiency and equilibrium time of 217.81 mg/g and 60 min, respectively. Its antifungal activity, for the first time, was investigated against Penicillium notatum, Aspergillus flavus, Aspergillus fumigatus, Aspergillus niger, and Mucor fungi at various concentrations (1000-1.95 µg/mL). This LDH was found to be effective against a variety of fungal strains, particularly Penicillium and Mucor species and showed zones of inhibition of 19.3 and 21.6 mm for Penicillium and Mucor, respectively, with an inhibition of 85% for Penicillium species and 68.3% for Mucormycosis. The highest antifungal efficacy results were obtained at very low MIC concentrations (33.3 and 62 µg/ml) against Penicillium and Mucor, respectively. The results of this study suggest a promising multifunctional potential of this LDH for water and wastewater treatment and disinfection applications.

Antimicrobial properties of promising Zn-Fe based layered double hydroxides for the disinfection of real dairy wastewater effluents.

Bacterial resistance to conventional antibiotics is a serious challenge that requires novel antibacterial agents. Moreover, wastewater from dairy farms might contain countless number of pathogens, organic contaminants and heavy metals that consider a threat to the terrestrial and aquatic environment. Therefore, the development of cost-effective, highly operation-convenient, recyclable multifunctional antimicrobial agents became an urgent necessity. Layered double hydroxides (LDH) have shown promising results as antibacterial agents. However, more work is required to further investigate and improve the antimicrobial performance of LDH structures against pathogens. In this study three Zn-Fe based LDH were investigated for real dairy wastewater disinfection. The three LDH samples were cobalt substituted Zn-Fe LDH (CoZnFe), magnesium substituted Zn-Fe LDH (MgZnFe) and MgZnFe-Triazol LDH (MgZnFe-Tz) nanocomposite. Seventy-five wastewater samples were collected from a dairy farm sewage system. The sensitivity of isolated pathogens was tested against two commonly used disinfectants (Terminator and TH4) and was assessed against the three LDH samples at different concentrations. The overall prevalence of S. agalactiae, S. dysgalactiae and Staph. aureus was significantly at 80.0% (P-value = 0.008, X2 = 9.700). There was variable degree of resistance to the tested disinfectants, whereas the antimicrobial activity of CoZnFe LDH was increased significantly at a concentration of 0.005 mg/L followed by MgZnFe LDH while MgZnFe-Tz LDH showed minor antibacterial potency. It was concluded that CoZnFe LDH showed a better biocidal activity in killing the isolated resistant pathogens, making it a good choice tool in combating the zoonotic microbes in wastewater sources.

Cost estimation of synthesis and utilization of nano-adsorbents on the laboratory and industrial scales: A detailed review.

The recent regulations pertaining to the circular economy have unlocked new prospects for researchers. In contrast to the unsustainable models associated with the linear economy, integration of concepts of circular economy braces reducing, reusing, and recycling of waste materials into high-end products. In this regard, adsorption is a promising and cost-effective water treatment technology for handling conventional and emerging pollutants. Numerous studies are published annually to investigate the technical performance of nano-adsorbents and nanocomposites in terms of adsorption capacity and kinetics. Yet, economic performance evaluation is rarely discussed in the literature. Even if an adsorbent shows high removal efficiency towards a specific pollutant, its high preparation and/or utilization costs might hinder its real-life use. This tutorial review aims at illustrating cost estimation methods for the synthesis and utilization of conventional and nano-adsorbents. The current treatise discusses the synthesis of adsorbents on a laboratory scale where the raw material, transportation, chemical, energy, and any other costs are discussed. Moreover, equations for estimating the costs at the large-scale adsorption units for wastewater treatment are illustrated. This review focuses on introducing these topics to non-specialized readers in a detailed but simplified manner.

Waste Valorization of a Recycled ZnCoFe Mixed Metal Oxide/Ceftriaxone Waste Layered Nanoadsorbent for Further Dye Removal.

Waste valorization of spent wastewater nanoadsorbents is a promising technique to support the circular economy strategies. The terrible rise of heavy metal pollution in the environment is considered a serious threat to the terrestrial and aquatic environment. This led to the necessity of developing cost-effective, operation-convenient, and recyclable adsorbents. ZnCoFe mixed metal oxide (MMO) was synthesized using co-precipitation. The sample was characterized using X-ray powder diffraction, Fourier transform infrared spectroscopy, and scanning electron microscopy. Factors affecting the adsorption process such as pH, the dose of adsorbent, and time were investigated. ZnCoFe MMO showed the maximum adsorption capacity of 118.45 mg/g for ceftriaxone sodium. The spent MMO was recycled as an adsorbent for malachite green (MG) removal. Interestingly, the spent adsorbent showed 94% removal percent for MG as compared to the fresh MMO (90%). The kinetic investigation of the adsorption process was performed and discussed. In addition, ZnCoFe MMO was tested as an antimicrobial agent. The proposed approach opens up a new avenue for recycling wastes after adsorption into value-added materials for utilization in adsorbent production with excellent performance as antimicrobial agents.

Valorization of spent double substituted Co-Ni-Zn-Fe LDH wastewater nanoadsorbent as methanol electro-oxidation catalyst.

Finding suitable non-expensive electrocatalyst materials for methanol oxidation is a significant challenge. Waste valorization of spent wastewater nanoadsorbents is a promising route toward achieving circular economy guidelines. In this study, the residual of layered double hydroxide (LDH) can be used as an electrocatalyst in direct methanol fuel cells as a novel approach. The Co-Ni-Zn-Fe LDH was prepared by the co-precipitation method followed by the adsorption of methyl orange (MO). Moreover, the spent adsorbent was calcined at different temperatures (200, 400, and 600 °C) to be converted to the corresponding mixed metal oxides (MMO). The prepared samples were characterized using XRD, FTIR, HRTEM, zeta potential, and hydrodynamic size measurements. The spent adsorbent was tested as an electro-catalyst for direct methanol electro-oxidation. The spent LDH/MO adsorbent showed a maximum current density of 6.66 mA/cm2 at a 50 mV/s scan rate and a 1 M methanol concentration. The spent MMO/MO adsorbent showed a maximum current density of 8.40 mA/cm2 at a 200 °C calcination temperature, 50 mV/s scan rate, and a 3 M methanol concentration. Both samples show reasonable stability over time, as indicated by the chronoamperometric response. Further nanoengineering of used nanoadsorbents could be a promising path to repurposing these wastes as electro-oxidation catalysts.

Prostate Cancer Cellular Uptake of Ternary Titanate Nanotubes/CuFe2O4/Zn-Fe Mixed Metal Oxides Nanocomposite.

BACKGROUND: Certainly, there is a demand for stronger recognition of how nanoparticles can move through the cell membrane. Prostate cancer is one of the forcing sources of cancer-relevant deaths among men. AIM OF THE WORK: The current research studied the power of prostate cancer cells to uptake a ternary nanocomposite TNT/CuFe2O4/Zn-Fe mixed metal oxides (MMO). METHODOLOGY: The nanocomposite was synthesized by a chemical method and characterized by a High-resolution transmission electron microscope, Field emission scanning electron microscope, X-ray diffraction, Fourier transmission infra-red, X-ray photoelectron spectroscopy, dynamic light scattering. Besides, it was implemented as an inorganic anticancer agent versus Prostate cancer PC-3 cells. RESULTS: The results revealed cellular uptake validity, cell viability reduction, ultra-structures alterations, morphological changes and membrane damage of PC-3 cells. CONCLUSION: The prepared ternary nanocomposite was highly uptake by PC-3 cells and possessed cytotoxicity that was dose and time-dependent. To conclude, the study offered the potential of the investigated ternary nanocomposite as a promising prostate anticancer agent.

Acceleration of ammonium phosphate hydrolysis using TiO2 microspheres as a catalyst for hydrogen production.

Titania microspheres are considered an adequate material with low cost and easily attainable pathways, and can be utilized in photocatalytic H2 production to solve the energy crisis. Spherical porous titanium dioxide materials, with nanostructure composition, were chemically synthesized from titanate nanotubes via a simple hydrothermal technique, then added as a catalyst to accelerate the route of ammonium phosphate hydrolysis for hydrogen production. The mechanism of sphere formation from titanate nanotubes is elucidated in detail through the current study. The prepared materials were applied as a photocatalyst to facilitate the separation and transfer of photoinduced electrons, while preventing the recombination of electron-hole pairs. Experimental results show that the obtained microspheres possess significantly enhanced photocatalytic hydrogen (H2) production performance. The amount of photocatalytic hydrogen product using the microspheres is found to be ∼2.5 fold greater than that of titanate nanotubes. Analytical techniques such as field-emission scanning electron microscopy (FESEM), high-resolution transmission electron microscopy (HR-TEM), simulated visible solar light and X-ray diffraction (XRD) were used for the evaluation and characterization of the developed products, as well as the elucidation of the route of hydrolysis in the hydrogen production process.

Gamma radiation as a green method to enhance the dielectric behaviour, magnetization, antibacterial activity and dye removal capacity of Co-Fe LDH nanosheets.

Nowadays, improving the physico-chemical properties of nanomaterials to enhance their performance towards various applications is urgent. Accordingly, gamma irradiation (GI) has evolved and attracted wide attention as a promising green technique to meet this need. In the current study, a Co-Fe LDH was used as a model 2D nanomaterial and was irradiated by GI (dose = 100 kGy). The sample was characterized via XRD, FTIR, FESEM, HRTEM, hydrodynamic size, zeta potential, and BET surface area measurements. The results showed that after irradiation, the surface area of the sample increased from 83 to 89 m2 g-1. Moreover, irradiation increased its dielectric constant, dielectric loss and AC conductivity. In addition, the sample showed superparamagnetic behavior, where its saturation magnetization increased from 1.28 to 52.04 emu g-1 after irradiation. Furthermore, the adsorption capacity of the irradiated LDH towards malachite green (MG) and methylene blue (MB) as model wastewater pollutants was also studied. The exposure of LDH to GI enhanced its adsorption capacity for MG from 44.73 to 54.43 mg g-1. The Langmuir-Freundlich, Sips, and Baudu models were well suited for both MG and MB adsorption among the six fitted isotherm models. The pseudo-first and second order models fit the adsorption kinetics better than the intraparticle diffusion model for both dyes. The interaction of MB and MG with the LDH surface was further investigated in dry and aqueous solution using Grand canonical Monte Carlo and molecular dynamics simulations. These two techniques provided insight into the adsorption mechanism, which is vital to understand the adsorption process by the LDH nanosheets and their possible use in practical applications. Moreover, the Co-Fe LDH showed good antibacterial activity against both Gram-positive and Gram-negative bacteria strains. Furthermore, due to its magnetic property, the Co-Fe LDH could be simply recovered from water by magnetic separation at a low magnetic field after the adsorption process.