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Eriochrome Black T (EBT) and chromium (Cr) are considered to be potential pollutants due to their toxicity and severe impact on the environment. In the current study, hydrotalcite-derived Mg-Ca-Al-LDO mixed metal oxide composite was prepared using a conventional co-precipitation method and explored in terms of the removal of Cr and EBT dye from aqueous solution in a batch mode adsorption process. The prepared Mg-Ca-Al-LDH, Mg-Ca-Al-LDO and spent Mg-Ca-Al-LDO adsorbents were characterized to propose the adsorption mechanism. Different adsorption parameters were examined, such as adsorbent dosage, initial concentration, pH, reaction temperature and contact time. The EBT adsorption kinetic results matched strongly with the pseudo-second-order model for both Cr (R2 = 0.991) and EBT (R2 = 0.999). The Langmuir isotherm model exhibited a maximum adsorption capacity of 65.5 mg/g and 150.3 mg/g for Cr and EBT, respectively. The structure and morphology results obtained after Cr and EBT dye adsorption reveal that the adsorption mechanism is associated with electrostatic interactions and surface complexation of Cr and EBT dye with Mg-Ca-Al-LDO surface functional groups. Moreover, more than 84% of the initial adsorption capacity of EBT and Cr can be achieved on the Mg-Ca-Al-LDO surface after five adsorption/desorption cycles. Finally, the Mg-Ca-Al-LDO mixed metal oxide composite can be potentially used as a cost-effective adsorbent for wastewater treatment processes.

Increased phosphate concentration in water bodies has led to eutrophication, and its removal is an inevitable requirement of sustainable wastewater purification systems. In this study, MgAl layered doubled hydroxide (LDH) composites doped on the surface of activated carbon (AC/MgAl LDH) with various (Mg + Al) total metal loading (5 wt%, 10 wt%, and 15 wt%) were prepared by the co-precipitation method. The influence of (Mg + Al) total metal loading onto AC was examined to remove phosphate ions from aqueous solutions. The effect of adsorption parameters, including adsorbent dosage, initial solution pH, initial phosphate concentration, contact time, and experiment temperature, were investigated via batch adsorption experiments. The adsorption results demonstrated that the phosphate adsorption capacity significantly improved with increasing the (Mg + Al) metal loading on the surface of AC. The maximum Langmuir phosphate adsorption capacity was 337.2 mg phosphate per gram of AC/MgAl-3 LDH composite (15 wt% Mg + Al) composite at pH ~6.3, 22 °C, and 1 g/L of adsorbent. The kinetic data were best fitted with the pseudo-second order model. The initial solution pH notably influenced the phosphate removal by AC/MgAl-3 LDH composite with a maximum removal at pH 2.3. According to the spent adsorbent characterization results, the dominant mechanisms of phosphate removal by AC/MgAl-3 LDH were electrostatic interactions, ion exchange, and inner-sphere complexation. The phosphate adsorption capacity was gradually increased with increasing the experiment temperature, suggesting an endothermic adsorption process. Overall, the AC/MgAl LDH composites pave the way for an effective strategy for phosphate removal from aqueous solutions.

In the current study, preparation of cobalt-aluminum layered double oxide doped activated carbon (Co-Al LDO/AC) was achieved by the co-precipitation technique and utilized for the remediation of lead (Pb 2+ ) from water. Various methods were employed to examine the properties of the composite material, including BET, XRD, FTIR, SEM, and EDS analysis. The material characterization outcomes indicated that the LDO structure was successfully incorporated into the AC matrices with a surface area of 189.4 m 2 /g. The influence of adsorption parameters including Co-Al LDO/AC dosage, period of contact, initial Pb 2+ loading, and initial solution pH were investigated. Moreover, the isotherm and kinetic models were investigated to provide a deeper understanding of the elimination mechanism of Pb 2+ ions. The adsorption results illustrated that pH has a substantial influence on Pb 2+ removal with a highest removal effectiveness at pH = 6 and a fast adsorption rate within 7 h. The kinetic data were well aligned with the pseudo-second-order model while the isotherm data obeyed the Sips model (R 2 >0.966). The highest adsorption uptake, estimated by the Sips model was 25.09 mg/g. Considering the modeling and characterization of the spent Co-Al LDO/AC, a chemical interaction process was involved in the elimination process and mainly controlled by ion exchange, electrostatic interactions, and surface complexation mechanisms. Accordingly, the Co-Al LDO/AC could have great potential as a promising hybrid for the purification of toxic Pb 2+ ions from contaminated water streams.

Pretreatment of raw feed water is an essential step for proper functioning of a reverse osmosis (RO) desalination plant as it minimizes the risk of membrane fouling. Conventional pretreatment methods have drawbacks, such as the potential of biofouling, chemical consumption, and carryover. Non-conventional membrane-based pretreatment technologies have emerged as promising alternatives. The present review focuses on recent advances in MF, UF, and NF membrane pretreatment techniques that have been shown to be effective in preventing fouling as well as having low energy consumption. This review also highlights the advantages and disadvantages of polymeric and ceramic membranes. Hybrid technologies, which combine the benefits of conventional and non-conventional methods or different membranes, are also discussed as a potential solution for effective pretreatment. The literature that has been analyzed reveals the challenges associated with RO pretreatment, including the high cost of conventional pretreatment systems, the difficulty of controlling biofouling, and the production of large volumes of wastewater. To address these challenges, sustainable hybrid strategies for ceramic membrane-based systems in RO pretreatment are proposed. These strategies include a thorough assessment of the source water, removal of a wide range of impurities, and a combination of methods such as adsorption and carbon dioxide with a low amount of antiscalants. Furthermore, the suggestion of incorporating renewable energy sources such as solar or wind power can help reduce the environmental impact of the system. A pilot study is also recommended to overcome the difficulties in scaling ceramic systems from laboratory to industrial scale. The review also emphasizes the importance of conducting an effective assessment to suggest a treatment for the brine if needed before being discharged to the environment. By following this framework, sustainable, energy-efficient, and effective solutions can be recommended for pretreatment in desalination systems, which can have significant implications for water scarcity and environmental sustainability.

Density functional theory (DFT) calculations have been utilized to evaluate the complete reaction mechanism of methane dry reforming (DRM) over Ni2Cu (111) bimetallic catalyst. The detailed catalytic cycle on Ni2Cu (111) catalyst demonstrated superior coke resistance compared to pure Ni (111) and Ni2Fe (111) reported in the literature. Doping Cu in the Ni–Ni network enhanced the competitive CH oxidation by both atomic O and OH species with the latter having only 0.02 eV higher than the 1.06 eV energy barrier required for CH oxidation by atomic O. Among the C/CH oxidation pathways, C* + O* → CO (g) was the most favorable with an energy barrier of 0.72 eV. This was almost half of the energy barrier required for the rate-limiting step of CH decomposition (1.40 eV) and indicated enhanced coke deposition removal. Finally, we investigated the effect of temperature (800~1000 K) on the carbon deposition and elimination mechanism over Ni2Cu (111) catalyst. Under those realistic DRM conditions, the calculations showed a periodic cycle of simultaneous carbon deposition and elimination resulting in improved catalyst stability.

Alizarin Red and Rhodamine B are widely used dyes in the textile, paper, and plastic industries. However, the disposal or release of these dyes into the environment can negatively impact on both the environment and human health. In the present study, oxidized carbon nanotubes (OCNT) were used to eliminate Alizarin Red and Rhodamine B from contaminated water in batch adsorption experiments. The adsorption outcomes suggested that OCNT has the potential to be an effective material for the removal of these dyes from contaminated water. The kinetics modeling revealed that the adsorption process of both dyes onto OCNT follows the pseudo-second-order model, indicating a chemisorption process. Moreover, the OCNT has indicated fast kinetics in which the equilibrium was achieved in 4 h. The isotherm study demonstrated that the Freundlich isotherm model best fits the experimental data, suggesting that dyes’ adsorption onto OCNT is a monolayer adsorption process. The maximum adsorption capacities were 124.7 and 614.7 mg/g for Rhodamine B and Alizarin Red, respectively. The adsorption of these dyes was found to be more efficient at pH values of 6-8. This study suggests that OCNT can be an effective adsorbent for removing Alizarin Red and Rhodamine B from contaminated water.

The authors would like to make the following correction to the published paper [...]

Selecting a sustainable source of silica from biomass waste was the research challenge that was put forth in this investigation. Herein, the MCM-41 support has been synthesized using a renewable rice husk and explored as a support for Ni-Cu catalyst in the production of zero-emission H2 through CH4 pyrolysis. The role of Cu promoter was investigated by doping different amounts of Cu loading to 30wt%Ni/R-MCM-41catalyst, which improved the catalytic performance in terms of CH4 conversion and stability. An optimum Cu loading of 3wt% addition to 30wt%Ni/R-MCM-41 catalyst demonstrated the best catalytic performance compared to all the catalysts in terms of hydrogen yield (15,218 mol H2/mol Ni) and carbon formation rate. The Ni-Cu alloy formation was confirmed by X-ray diffraction, H2-temperature programmed reduction, and pulse chemisorption studies, as demonstrated by decreased H2 uptake (from 41 to 33 μmol/gcat) and enhanced N2O (from 89.2 to 138.3 μmol/g) uptakes, which results in a significant improvement in the availability of the surface metal species (both Cu and Ni), which in turn contributed to increase the CH4 cracking performance and stabilization of Ni species. Additionally, doping Cu results in better carbon nanotube production, as shown by the lowest ID/IG ratio from the Raman spectroscopic analysis.Selecting a sustainable source of silica from biomass waste was the research challenge that was put forth in this investigation. Herein, the MCM-41 support has been synthesized using a renewable rice husk and explored as a support for Ni-Cu catalyst in the production of zero-emission H2 through CH4 pyrolysis. The role of Cu promoter was investigated by doping different amounts of Cu loading to 30wt%Ni/R-MCM-41catalyst, which improved the catalytic performance in terms of CH4 conversion and stability. An optimum Cu loading of 3wt% addition to 30wt%Ni/R-MCM-41 catalyst demonstrated the best catalytic performance compared to all the catalysts in terms of hydrogen yield (15,218 mol H2/mol Ni) and carbon formation rate. The Ni-Cu alloy formation was confirmed by X-ray diffraction, H2-temperature programmed reduction, and pulse chemisorption studies, as demonstrated by decreased H2 uptake (from 41 to 33 μmol/gcat) and enhanced N2O (from 89.2 to 138.3 μmol/g) uptakes, which results in a significant improvement in the availability of the surface metal species (both Cu and Ni), which in turn contributed to increase the CH4 cracking performance and stabilization of Ni species. Additionally, doping Cu results in better carbon nanotube production, as shown by the lowest ID/IG ratio from the Raman spectroscopic analysis.

Eriochrome Black T (EBT) and chromium (Cr) are considered to be potential pollutants due to their toxicity and severe impact on the environment. In the current study, hydrotalcite-derived Mg-Ca-Al-LDO mixed metal oxide composite was prepared using a conventional co-precipitation method and explored in terms of the removal of Cr and EBT dye from aqueous solution in a batch mode adsorption process. The prepared Mg-Ca-Al-LDH, Mg-Ca-Al-LDO and spent Mg-Ca-Al-LDO adsorbents were characterized to propose the adsorption mechanism. Different adsorption parameters were examined, such as adsorbent dosage, initial concentration, pH, reaction temperature and contact time. The EBT adsorption kinetic results matched strongly with the pseudo-second-order model for both Cr (R[sup.2] = 0.991) and EBT (R[sup.2] = 0.999). The Langmuir isotherm model exhibited a maximum adsorption capacity of 65.5 mg/g and 150.3 mg/g for Cr and EBT, respectively. The structure and morphology results obtained after Cr and EBT dye adsorption reveal that the adsorption mechanism is associated with electrostatic interactions and surface complexation of Cr and EBT dye with Mg-Ca-Al-LDO surface functional groups. Moreover, more than 84% of the initial adsorption capacity of EBT and Cr can be achieved on the Mg-Ca-Al-LDO surface after five adsorption/desorption cycles. Finally, the Mg-Ca-Al-LDO mixed metal oxide composite can be potentially used as a cost-effective adsorbent for wastewater treatment processes.

Selecting a sustainable source of silica from biomass waste was the research challenge that was put forth in this investigation. Herein, the MCM-41 support has been synthesized using a renewable rice husk and explored as a support for Ni-Cu catalyst in the production of zero-emission H through CH pyrolysis. The role of Cu promoter was investigated by doping different amounts of Cu loading to 30wt%Ni/R-MCM-41catalyst, which improved the catalytic performance in terms of CH conversion and stability. An optimum Cu loading of 3wt% addition to 30wt%Ni/R-MCM-41 catalyst demonstrated the best catalytic performance compared to all the catalysts in terms of hydrogen yield (15,218 mol H /mol ) and carbon formation rate. The Ni-Cu alloy formation was confirmed by X-ray diffraction, H -temperature programmed reduction, and pulse chemisorption studies, as demonstrated by decreased H uptake (from 41 to 33 μmol/g ) and enhanced N O (from 89.2 to 138.3 μmol/g) uptakes, which results in a significant improvement in the availability of the surface metal species (both Cu and Ni), which in turn contributed to increase the CH cracking performance and stabilization of Ni species. Additionally, doping Cu results in better carbon nanotube production, as shown by the lowest I /I ratio from the Raman spectroscopic analysis.