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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. [ABSTRACT FROM AUTHOR]

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. [ABSTRACT FROM AUTHOR]

In this work, the MCM-48 mesoporous material was prepared and characterized to apply it as an active adsorbent for the adsorption of 4-nitroaniline (4-Nitrobenzenamine) from wastewater. The MCM-48 characterizations were specified by implementing various techniques such as; scanning electron microscopy (SEM), Energy dispersive X-ray analysis (EDAX), X-ray diffraction (XRD), Brunauer–Emmett–Teller (BET) surface area, pore size distribution (PSD), and Fourier transform infrared (FTIR). The batch adsorption results showed that the MCM-48 was very active for the 4-nitroaniline adsorption from wastewater. The adsorption equilibrium results were analyzed by applying isotherms like Langmuir, Freundlich, and Temkin. The maximum experimental uptake according to type I Langmuir adsorption was found to be 90 mg g−1 approximately. The Langmuir model with determination coefficient R2 = 0.9965 is superior than the Freundlich model R2 = 0.99628 and Temkin model R2 = 0.9834. The kinetic adsorption was investigated according to pseudo 1st order, pseudo 2nd order, and Intraparticle diffusion model. The kinetic results demonstrated that the regression coefficients are so high R2 = 0.9949, that mean the pseudo 2nd order hypothesis for the adsorption mechanism process appears to be well-supported. The findings of adsorption isotherms and kinetics studies indicate the adsorption mechanism is a chemisorption and physical adsorption process. [ABSTRACT FROM AUTHOR]

ZnO is a semiconductor material that has important physical and chemical properties, which are frequently and significantly enhanced by the addition of impurities, such as doping. A study of the structural properties of pristine and functionalized (i.e., doped with Antimony and Tungsten) ZnO nanoparticles has been conducted for the photocatalyst-based degradation of methylene blue (MB) dye under both Ultraviolet (UV) and solar light. Authors have used a 1% concentration of dopant for doping purposes. The synthesized materials were characterized for structural analysis, functional group identification, spectroscopic measurements, and morphological examination using X-ray diffraction (XRD), Fourier transform-infrared (FTIR), UV-Vis spectroscopy (UV-Vis), and Field emission scanning electron microscope (FESEM) techniques. XRD analysis confirmed that the synthesized-doped materials retained the wurtzite hexagonal structure with a purity of 99%. Transmission electron microscope (TEM) analysis data reveals the average size of pure ZnO-NPs was found to be 7 nm; after doping the size was found to be increased to 18 nm and 9.55 nm, respectively, for ZnO-W and ZnO-Sb. As per FESEM analysis results, minor morphological changes were observed after doping. The Ultraviolet Differential reflectance spectroscopy UV-DRS study revealed the confirmation of ZnO doping with antimony and tungsten, which exhibited a blue shift. The decrease in the band-gap on doping makes the ZnO-NPs more efficient for photocatalytic applications. The photocatalytic efficiency of pristine and doped ZnO-NPs catalysts for methylene blue photocatalytic degradation (PCD) was analyzed under both UV and solar irradiation. This study analyzed the effect of pH, nano-photocatalyst dose, and initial dye concentration (ICD) on the PCD of MB. The obtained analytical results showed that the ideal conditions for the PCD of MB dye are as follows: pH = 9, the quantity of the nano-photocatalyst used was 300 mg/L, and an initial MB dye dose of 10 ppm. These conditions lead to a PCD of about 91% of the MB dye by using ZnO-Sb nano-photocatalyst on exposure to solar radiation. The reusability study also revealed the stability of nano-photocatalysts. The current research may pave the way for the removal of hazardous dyes from wastewater discharged by many industries. [ABSTRACT FROM AUTHOR]

Removal of AffiliationIn the original publication [[1]], there was an error regarding the affiliation for Abdelfattah Amari; the updated affiliation should include: Department of Chemical Engineering, College of Engineering, King Khalid University, Abha 61411, Saudi Arabia. The authors state that the scientific conclusions are unaffected. This correction was approved by the Academic Editor.By Hind F. Hasan; Farah T. Al-Sudani; Talib M. Albayati; Issam K. Salih; Hamed N. Harharah; Hasan Sh. Majdi; Noori M. Cata Saady; Sohrab Zendehboudi and Abdelfattah AmariReported by Author; Author; Author; Author; Author; Author; Author; Author; Author [Extracted from the article]