Activated carbon-alginate beads impregnated with surfactant as sustainable adsorbent for efficient removal of methylene blue

A cost-effective and sustainable Calligonum polygonoides biomass based activated carbon (AC) was synthesized. The prepared AC was utilized in the fabrication of carbon-alginate beads for the adsorption of methylene blue (MB) textile dye from aqueous solution. The surface morphology, surface functional groups, elemental analysis and thermal behavior of the prepared beads were investigated using different analytical techniques. Batch adsorption experiments were performed to investigate the adsorption capacity of the beads. Effect of different parameters such as initial pH of MB solution, dose of adsorbent, contact time, initial concentration of MB and temperature were evaluated. The kinetic studies identified pseudo-second order model. Langmuir and Freundlich isotherm models were applied and fitted to the experimental equilibrium data. The beads showed a maximum adsorption capacity of 769 mg/g in basic pH at 30 °C while using 400 mg·L-1 of MB solution. The adsorption process was found to be endothermic and spontaneous as confirmed by the thermodynamic data. The fabricated beads were subjected to recycling which exhibited same adsorption efficiency after six regeneration cycles. The results showed that the AC-alginate beads impregnated with SDS have high adsorption capability and would be used for the efficient removal of cationic dyes from wastewater

Exploring copyrolysis characteristics and thermokinetics of peach stone and bituminous coal blends

Copyrolysis, being an active area of research due to its synergistic impact in utilizing diverse fuel resources, including waste materials, like, peach stone (PS), has been the focal point for this study. PS, produced in vast quantities annually and typically intended for landscaping or insulation purposes, is being studied in combination with low‐grade bituminous coal for energy utilization focusing on thermokinetics and synergistic aspects. Coal‐peach stone (C‐PS) blends were formulated at different ratios and subjected to comprehensive characterization techniques, including ultimate analysis (CHN‐S), gross calorific value (GCV), Fourier transform infrared spectroscopy, and thermogravimetric analyzer (TGA). The ultimate analysis revealed an enhancement in carbon and hydrogen content from 45.38% to 68.08% and from 3.89% to 6.96%, respectively. Additionally, a reduction in sulfur and nitrogen content from 0.54% to 0.11% and from 1.16% to 0.42%, respectively, was observed with an increase in the ratio of PS in the C‐PS blends. The GCV of C‐PS blends ranged from 20.75 to 26.01 MJ kg−1. The pyrolysis conditions simulated in TGA are pivotal for evaluating thermokinetics and synergistic effects. The 60C:40PS blend shows a positive synergy index (SI) value of 0.0203% concerning total mass loss (MLT) indicating a favorable condition for bio‐oil generation. Coats–Redfern model‐fitting method reveals that the activation energy (Ea) of C‐PS blends increases in Section II with the addition of PS, and conversely, it decreases in Section III. The Ea for 100PS and 100C was 106.76 and 45.85 kJ mol−1 through (D3) and (F1), respectively, which was improved through the optimal blend 60C:40PS with an Ea of 94.56 and 27.58 kJ mol−1 through (D3) and (F2), respectively. The values obtained from linear regression prove that the kinetic models are effective while the thermodynamic analysis indicates that the pyrolytic behavior of C‐PS blends is characterized as endothermic, nonspontaneous, and capable of achieving thermodynamic equilibrium more rapidly

Synthesis of Boron-Doped Zinc Oxide Nanosheets by Using Phyllanthus Emblica Leaf Extract: A Sustainable Environmental Applications

The use of Phyllanthus emblica (gooseberry) leaf extract to synthesize Boron-doped zinc oxide nanosheets (B-doped ZnO-NSs) is deliberated in this article. Scanning electron microscopy (SEM) shows a network of synthesized nanosheets randomly aligned side by side in a B-doped ZnO (15 wt% B) sample. The thickness of B-doped ZnO-NSs is in the range of 20–80 nm. B-doped ZnO-NSs were tested against both gram-positive and gram-negative bacterial strains including Staphylococcus aureus, Pseudomonas aeruginosa, Klebsiella pneumonia, and Escherichia coli. Against gram-negative bacterium (K. pneumonia and E. coli), B-doped ZnO displays enhanced antibacterial activity with 26 and 24 mm of inhibition zone, respectively. The mass attenuation coefficient (MAC), linear attenuation coefficient (LAC), mean free path (MFP), half-value layer (HVL), and tenth value layer (TVL) of B-doped ZnO were investigated as aspects linked to radiation shielding. These observations were carried out by using a PTW® electron detector and VARIAN® irradiation with 6 MeV electrons. The results of these experiments can be used to learn more about the radiation shielding properties of B-doped ZnO nanostructures

Carbon nanofibers based copper/zirconia catalysts for carbon dioxide hydrogenation to methanol: Effect of copper concentration

A series of novel bimetallic copper/zirconia carbon nanofibers supported catalysts with different Cu contents (5–25 wt%) were synthesized via deposition precipitation method. The physicochemical characterization of the calcined catalysts was carried out by X-ray diffraction, inductively coupled plasma optical emission spectroscopy, N2 adsorption–desorption, N2O chemisorption, temperature programmed reduction, X-ray photoelectron spectroscopy, high resolution transmission electron microscopy and temperature programmed CO2 desorption. Structure-reactivity correlation for catalytic hydrogenation of CO2 to methanol was discussed in details. Reaction studies revealed 15 wt% as optimum Cu concentration for CO2 conversion to methanol with CO2/H2 feed volume ratio of 1:3. Cu surface area was found to play a vital role in methanol synthesis rate. CO2 conversion was observed to be directly proportional to the number of total basic sites. A comparative study of this novel catalyst with the recently reported data revealed the better CO2 conversion at relatively low reaction temperature

Ni-Based Catalyst for Carbon Dioxide Methanation: A Review on Performance and Progress

Catalytic conversion of CO2 into methane is an attractive method because it can alleviate global warming and provide a solution for the energy depletion crisis. Nickel-based catalysts were commonly employed in such conversions due to their high performance over cost ratio. However, the major challenges are that Ni tends to agglomerate and cause carbon deposition during the high-temperature reaction. In the past decades, extensive works have been carried out to design and synthesize more active nickel-based catalysts to achieve high CO2 conversion and CH4 selectivity. This review critically discusses the recent application of Ni-based catalyst for CO2 methanation, including the progress on the effect of supporting material, promoters, and catalyst composition. The thermodynamics, kinetics, and mechanism of CO2 methanation are also briefly addressed

Ni-Based Catalyst for Carbon Dioxide Methanation: A Review on Performance and Progress

Catalytic conversion of CO2 into methane is an attractive method because it can alleviate global warming and provide a solution for the energy depletion crisis. Nickel-based catalysts were commonly employed in such conversions due to their high performance over cost ratio. However, the major challenges are that Ni tends to agglomerate and cause carbon deposition during the high-temperature reaction. In the past decades, extensive works have been carried out to design and synthesize more active nickel-based catalysts to achieve high CO2 conversion and CH4 selectivity. This review critically discusses the recent application of Ni-based catalyst for CO2 methanation, including the progress on the effect of supporting material, promoters, and catalyst composition. The thermodynamics, kinetics, and mechanism of CO2 methanation are also briefly addressed

Cobalt ferrite for direct cracking of methane to produce hydrogen and carbon nanostructure: Effect of temperature and methane flow rate

Cobalt ferrite (CoFe2O4) was used as a catalyst for direct methane cracking. The reaction was accomplished in a fixed bed reactor at normal atmospheric pressure, while gas flow rate (20–50 mL/min) and reaction temperature (800–900 °C) were varied. The fresh CoFe2O4 morphology is sponge-like particle with inverse spinel structure as revealed from SEM and XRD results. The methane conversions and hydrogen formation rate were increased with reaction temperature, while catalyst stability and induction period decreased. Increases of gas flow rate > 20 mL/min led to a decrease the overall catalytic activity of CoFe2O4 for methane cracking. The XRD results of spent catalysts revealed that CoFe alloy was the active phase of methane cracking. TGA analysis showed that the largest amount of deposited carbon was 70.46 % at (20 mL/min, 900 °C), where it was 34.40 % at (50 mL/min, 800 °C). The deposited carbon has the shape of spherical carbon nanostructures and/or nano sprouts as observed with SEM. Raman data confirmed the graphitization type of the deposited carbon

Biosynthesis and antibacterial activity of MgO-NPs produced from Camellia-sinensis leaves extract

Magnesium oxides nanoparticles (MgO-NPs) were synthesized by a novel technique based on the leaf extract of Camellia sinensis (Green tea). The synthesized nanoparticles were evaluated for antibacterial activity (against both gram-positive and gram-negative pathogens) and therefore can be a suitable therapeutic alternative to the usage of antibiotics. The antibacterial activity of synthesized MgO-NPs is tested against clinical isolates of gram-negative ( Escherichia coli, Pseudomonas aeruginosa, Serratia mercescens, Klebsiella pneumoniae ) and gram-positive ( Staphylococcus aureus, Staphylococcus epidermidis, Streptococcus pyogenes ) pathogenic bacteria. Agar well diffusion assay data indicate that MgO-NPs exhibit antibacterial activity at all concentrations tested against both gram-negative and gram-positive pathogenic bacteria, producing zone of inhibition (ZOI) in the range of 9.6 ± 1.1 to 21.0 ± 1.5 mm diameters. The maximum response is observed at 25 μ g ml ^−1 concentration of MgO-NPs, producing a zone of inhibition ranging from 15 ± 1.2 mm ( E.coli ) mm to 21.0 ± 1.5 mm ( S. marcescens)