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This review article provides useful information on TiO2 and ZnO photocatalysts and their derivatives in removing organic contaminants such as dyes, hydrocarbons, pesticides, etc. Also, the reaction mechanisms of TiO2 and ZnO photocatalysts and their derivatives were investigated. In addition, the impact of adding metallic (e.g., Ag, Co, Pt, Pd, Cu, Au, and Ni) and non-metallic (e.g., C, N, O, and S) cocatalysts to their structure on the photodegradation efficiency of organic compounds was thoroughly studied. Moreover, the advantages and disadvantages of various synthesis procedures of ZnO and TiO2 nanocatalysts were discussed and compared. Furthermore, the impact of photocatalyst dosage, photocatalyst structure, contaminant concentration, pH, light intensity and wavelength, temperature, and reaction time on the photodegradation efficiency were studied. According to previous studies, adding metallic and non-metallic cocatalysts to the TiO2 and ZnO structure led to a remarkable enhancement in their stability and reusability. In addition, metallic and non-metallic cocatalysts attached to TiO2 and ZnO demonstrated remarkable photocatalytic efficiency in removing organic contaminants.

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Removal of organic pollutants and metal ions from produced water by adsorption, using prepared activated carbon (AC) from sewage sludge, with chemical activations using NaOH, KOH and ZnCl2 separately and pyrolysis at different temperatures (500, 600 and 700 °C). Pure sludge and prepared ACs were analyzed using FTIR and XRD. The results showed 18% crystallinity compared to that of commercial AC, which has 44% crystallinity. The results of FTIR demonstrate that the properties of the post-treated affect the final products depending on the method used and that it contains similar functional groups to those present in the commercial AC, but at a higher peak intensity. Adsorption treatments were carried out at 25, 35 and 45 °C solution temperatures. The results showed that the removal of pollutants from produced water using prepared AC with all types of chemical activations reached 99.5%, such as commercial AC with 0.06 g dosage of adsorbent at pyrolysis temperatures of 500 and 600 °C and a solution temperature of 25 °C. The obtained results refer to the mechanism of exothermic reaction and physical adsorption. It was observed that despite the lower dosage of adsorbent of 0.01 g, a sufficient treatment of pollutants was achieved. This reveals the effectiveness of using sewage sludge as a cheap adsorbent. Also, using pure sewage sludge, the adsorption data showed a 95.2% removal of the pollutants. This result indicated that pure sludge has an efficient adsorption capacity and can be utilized as a cheap and environmentally friendly material. For the removal of manganese and cadmium metal ions from the produced water, the resultant data showed that more than 90% of manganese was adsorbed and more than 97% of cadmium was adsorbed, especially when using pure sewage sludge and prepared activated carbon with NaOH chemical activation at pyrolysis temperatures of 500 °C and 600 °C.

MCM-41, a mesoporous silica with a high surface area and hexagonal structure, was synthesized, and commercial nano-silicon dioxide (SiO2) was used as a solid adsorbed in post-combustion CO2 capture. The CO2 adsorption experiments were conducted in a fixed-bed adsorption system using 5–15 vol.% CO2/N2 at a flow rate of 100 mL/min at varying temperatures (20–80 °C) and atmospheric pressure. Analyses (X-ray diffraction, nitrogen adsorption-desorption isotherms, Fourier-transform infrared spectroscopy, and transmission electron microscopy (TEM)) revealed that the synthesized MCM-41 has mesoporous characteristics: a high surface area and large pore volumes. The CO2 adsorption capacity of MCM-41 and commercial nano-SiO2 increased considerably with increasing CO2 concentration and temperature, peaking at 60 °C. Below 60 °C, dynamics rather than thermodynamics governed the adsorption. Increasing the temperature from 60 to 80 °C decreased the adsorption capacity, and the reaction became thermodynamically dominant. Additionally, compared with commercial nano-SiO2, the MCM-41 sorbent demonstrated superior regenerability and thermal stability.

This paper presents the theoretical and computation irreversibility investigation of the Ellis hybrid nanofluid flow (CuO-Al2O3 nanoparticles) model using both homogeneous and heterogeneous responses toward the horizontal porous stretching cylinder. The Joule heating, thermal radiation, and heat generation/absorption are all factors that affect thermal energy transport, all of which are explored. On the surface of the cylinder, the slip boundary conditions are enforced. Keeping in mind that the nonlinear partial differential equations (PDEs) are converted into nonlinear ordinary differential equations (ODEs), these ODEs are constructed from the mathematical flow model with the aid of proper transformations. With the help of the bvp4c MATLAB built-in method, the nonlinear system equations are tacked numerically. Graphical results are used to discuss the numerical aspects of different parameters. By increasing the curvature parameter, entropy generation increases while fluid velocity decreases. Elasticity and magnetic fields thin boundary layers. Realistically, as liquid porosity increases, momentum boundary layer diminishes.

In the present study, a ternary magnetic nanocomposite (SiO2/MnFe2O4/ZIF-8) was synthesized via the embedding of the SiO2/MnFe2O4 nanocomposite within the metal–organic framework (ZIF-8). The synthesized nanocomposite was characterized using suitable techniques including FT-IR, XRD, SEM, TEM, VSM, and BET. The nanocomposite showed a high surface area (SBET = 831 m2·g−1) and superparamagnetic behavior (23.7 emu·g−1). All characterization techniques confirmed the successful combination of three nanocomposite parts (MnFe2O4, SiO2, and ZIF-8). The nanocomposite was examined for the adsorption of organic dyes, malachite green (MG) and methyl red (MR), from aqueous solutions. The adsorption conditions including ionic strength, contact time, pH, and adsorbent dosage were optimized by studying their change effect. The SiO2/MnFe2O4/ZIF-8 nanocomposite showed high adsorption capacities (1000.03 and 1111.12 mg/g) for the removal of MG and MR, respectively, from water. The isotherm and kinetics studies indicated that the adsorption of MG and MR dyes on the surface of the SiO2/MnFe2O4/ZIF-8 nanocomposite followed the Langmuir isotherm model and pseudo-second-order kinetic model, suggesting the monolayer chemisorption mechanism. The reusability study of up to five successive cycles indicated the successful reuse of the SiO2/MnFe2O4/ZIF-8 adsorbent for dye removal from wastewater. The comparison of the present adsorbent to the previously reported adsorbents indicated that it is a promising adsorbent for dye adsorption from wastewater and must be investigated in the future for the removal of additional pollutants.

Persistent organic pollutants (POPs) have become a major global concern due to their large amount of utilization every year and their calcitrant nature. Due to their continuous utilization and calcitrant nature, it has led to several environmental hazards. The conventional approaches are expensive, less efficient, laborious, time-consuming, and expensive. Therefore, here in this review the authors suggest the shortcomings of conventional techniques by using nanoparticles and nanotechnology. Nanotechnology has shown immense potential for the remediation of such POPs within a short period of time with high efficiency. The present review highlights the use of nanoremediation technologies for the removal of POPs with a special focus on nanocatalysis, nanofiltration, and nanoadsorption processes. Nanoparticles such as clays, zinc oxide, iron oxide, aluminum oxide, and their composites have been used widely for the efficient remediation of POPs. Moreover, filtrations such as nanofiltration and ultrafiltration have also shown interest in the remediation of POPs from wastewater. From several pieces of literature, it has been found that nano-based techniques have shown complete removal of POPs from wastewater in comparison to conventional methods, but the cost is one of the major issues when it comes to nano- and ultrafiltration. Future research in nano-based techniques for POP remediation will solve the cost issue and will make it one of the most widely accepted and available techniques. Nano-based processes provide a sustainable solution to the problem of POPs.

Free laccase has limitations for its use in industrial applications that require laccase immobilization on proper support, to improve its catalytic activity. Herein, the nanoparticles of magnetic iron oxide (Fe3O4) and copper ferrite (CuFe2O4) were successfully used as support for the immobilization of free laccase, using glutaraldehyde as a cross-linker. The immobilization conditions of laccase on the surface of nanoparticles were optimized to reach the maximum activity of the immobilized enzyme. The synthesized free nanoparticles and the nanoparticle-immobilized laccase were characterized using different techniques, including X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscope (SEM), vibrating sample magnetometer (VSM), and thermogravimetric analysis (TGA). CuFe2O4 nanoparticles, as support, enhanced laccase activity compared to free laccase and Fe3O4 nanoparticle-immobilized laccase that appeared during the study of pH, temperature, and storage stability on free and immobilized laccase. The CuFe2O4 and Fe3O4 nanoparticle-immobilized laccase showed superior activity in a wide pH range, temperature range, and storage period, up to 20 days at 4.0 °C, when compared to free laccase. Additionally, the synthesized nanobiocatalysts were examined and optimized for the biodegradation of the anionic dye Direct Red 23 (DR23). HPLC analysis was used to confirm the dye degradation. The reusability of immobilized laccases for the biodegradation of DR23 dye was investigated for up to six successive cycles, with a decolorization efficiency over 70.0%, which indicated good reusability and excellent stability.

Several trusted tasks use consensus algorithms to solve agreement challenges. Usually, consensus agreements are used to ensure data integrity and reliability in untrusted environments. In many distributed networking fields, the Proof of Work (PoW) consensus algorithm is commonly used. However, the standard PoW mechanism has two main limitations, where the first is the high power consumption and the second is the 51% attack vulnerability. In this paper, we look to improve the PoW consensus protocol by introducing several proof rounds. Any given consensus node should resolve the game of the current round Roundi before participating in the next round Roundi+1. Any node that resolves the game of Roundi can only pass to the next round if a predetermined number of solutions has been found by other nodes. The obtained evaluation results of this technique show significant improvements in terms of energy consumption and robustness against the 51% and Sybil attacks. By fixing the number of processes, we obtained an energy gain rate of 15.63% with five rounds and a gain rate of 19.91% with ten rounds.

The removal of heavy metals from water has become a global environmental problem. Various materials have been applied as adsorbent to remove metals from water. In this field, nanomaterials have been gaining increasing interest due to their exceptional properties. In this work, we discuss the synthesis of a core-shell structure nanocomposite by the modification of magnetic chitosan (CS) (Fe3O4/CS) with polyethylenimine (PEI) to produce Fe3O4/CS/PEI composite for the adsorption of arsenic ions (As(V) and As(III)) from aqueous solution. The synthesized materials were characterized using X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), transmission electron microscope (TEM), and vibrating sample magnetometer (VSM). The results indicated the successful combination of three components of the nanocomposite. The adsorption conditions were optimized by studying the effect of different parameters included pH, contact time, initial concentration, and adsorbent dosage. The optimum adsorption pH was found to be 6.7 while the optimum adsorbent dosage was found to be 2.0 and 1.5 g/L for As(III) and As(V), respectively. The removal efficiency for the uptake of As(III) and As(V) ions over Fe3O4/CS/PEI nanocomposite at optimum conditions was found to be 99.5 and 99.7%, respectively. The experimental results were fitted using Freundlich’s and Langmuir’s isotherms. The data were more fitted to Langmuir isotherm providing a suggestion of monolayer adsorption with maximum adsorption capacity equal to 77.61 and 86.50 mg/g for the removal of As(III) and As(V), respectively. Moreover, linear regression coefficient (R2) indicated that the adsorption of arsenic ions over the synthesized magnetic nanocomposite obeyed pseudo 2nd order suggesting the chemisorption process. The reusability of the nanosorbent for arsenic uptake using sodium hydroxide as eluent was also assessed up to five cycles. Interestingly, Fe3O4/CS/PEI nanocomposite can be considered as a promising adsorbent for As ions’ removal from water and should be tested for the removal of other pollutants.

In this study, natural clay minerals with green appearance were treated with sulfuric acid. Mass percentage of acid (wt%), temperature (T), contact time (t) and liquid-to-solid mass ratio (R) are used as the prevailing factors that determine the extent of acid-activation. The values of these factors range from 15⁻50%, 60⁻90 °C, 1.5⁻6 h and 4⁻7, respectively. The study has focused on the structural changes as well as textural characteristics of the clay. Three activated clay samples were prepared under different treatment conditions. The samples were characterized using X-ray powder diffraction (XRD), fourier transform infrared (FTIR), scanning electron microscope (SEM), chemical analysis and N2 adsorption techniques. Characterization of the treated clay minerals exhibited significant structural changes to a greater extent of acid-activation, from being partially crystalline to being amorphous silica. The surface area and total pore volume of clay increased proportionally with the level of acid treatment. The average pore diameter behaved differently. During the strong acid treatment, a large increase in pore volume and the enlargement of the pore size distribution were observed. This suggests that considerable structural changes and partial destruction may have occurred in this condition. The removal of methylene blue, used as cationic dye, from aqueous solution by the batch adsorption technique on three prepared acid-activated clay samples was studied. The Langmuir model was found to agree well with the experimental data.