4 research outputs found
Methylene blue removal using a low-cost activated carbon adsorbent from tobacco stems: kinetic and equilibrium studies
The aim of this study was to prepare activated carbon from tobacco stalks using microwave heating. The prepared activated carbon was applied as an adsorbent in methylene blue (MB) removal from water. The optimum conditions for activated carbon preparation were a radiation power of 280 W for a period of 6 minutes after the impregnation of the precursor material with 30% ZnCl2 for 24 hours. The activated carbon yield and iodine number were 49.43% and 1,264.51 mg/g respectively. The activated carbon also had a point of zero charge of 5.81 with an adsorption capacity of 123.45 mg/g for MB. The optimum conditions for MB adsorption were a pH of 6.5 with an adsorbent dosage of 0.2 g/50 mL at 25 °C. The MB adsorption kinetics followed the pseudo second order kinetic model with the intra-particle diffusion model suggesting a two-step adsorption mechanism. The adsorption data also fitted well within the Langmuir adsorption isotherm model. Tobacco stalks can successfully be turned into an economically important product.</jats:p
Synthesis and application of a ternary composite of clay, saw-dust and peanut husks in heavy metal adsorption
The adsorption of a multi-component system of ferrous, chromium, copper, nickel and lead on single, binary and ternary composites was studied. The aim of the study was to investigate whether a ternary composite of clay, peanut husks (PH) and saw-dust (SD) exhibited a higher adsorption capacity than that of a binary system of clay and SD as well as a single component adsorbent of PH alone. The materials were used in their raw state without any chemical modifications. This was done to retain the cost effective aspect of the naturally occurring adsorbents. The adsorption capacities of the ternary composite for the heavy metals Fe2+, Cr3+, Cu2+, Ni2+ and Pb2+ were 41.7 mg/g, 40.0 mg/g, 25.5 mg/g, 41.5 mg/g and 39.0 mg/g, respectively. It was found that the ternary composite exhibited excellent and enhanced adsorption capacity compared with both a binary and single adsorbent for the heavy metals Fe2+, Ni2+ and Cr3+. Characterization of the ternary composites was done using Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD) and thermogravimetric analysis (TGA). Kinetic models and adsorption isotherms were also studied. The pseudo second order kinetic model and the Langmuir adsorption isotherm best described the adsorption mechanisms for the ternary composite towards each of the heavy metal ions.</jats:p
Application of Novel C-TiO2-CFA/PAN Photocatalytic Membranes in the Removal of Textile Dyes in Wastewater
The existence of dye effluent in environmental water bodies is becoming a growing concern to environmentalists and civilians due to negative health effects. In this study, a novel poly(acrylonitrile)-membrane-supported carbon-doped titanium dioxide–coal fly ash nanocomposite (C-TiO2-CFA/PAN) was prepared and evaluated in the removal of textiles dyes (methyl orange and golden yellow) in water. The C-TiO2-CFA nanocomposite was prepared via sol-gel synthesis and immobilized on PAN membrane prepared via phase inversion technique. The photocatalyst was characterized by FTIR, XRD, BET surface area analysis, SEM, EDX, and DRS. FTIR analysis confirmed the existence of the expected functional groups, and XRD revealed that the C-TiO2 was predominantly in the anatase phase, which exhibited the highest photocatalytic activity. The optimum C-TiO2-CFA photocatalyst load on the PAN membrane was 2% w/w, and it achieved degradation efficiencies of 99.86% and 99.20% for MO and GY dyes, respectively, at pH 3.5, using a dye concentration of 10 ppm, under sunlight irradiation, in 300 min. The novel 2% C-TiO2-CFA/PAN photocatalytic membrane proved to be very effective in the removal of textile dyes’ water. Three reusability cycles were carried out, and no significant changes were observed in the photocatalytic efficiencies. Immobilization on PAN membrane allowed easy recovery and reuse of the photocatalyst
The Physical and Chemical Properties of Fine Carbon Particles-Pinewood Resin Blends and Their Possible Utilization
The application of biomass gasification technology is very important in the sense that it helps to relieve the dwindling supply of natural gas from fossil fuels, and the desired product of its gasification process is syngas. This syngas is a mixture of CO and H2; however, by-products such as char, tar, soot, ash, and condensates are also produced. This study, therefore, investigated selected by-products recovered from the gasification process of pinewood chips with specific reference to their potential application in other areas when used as blends. Three samples of the gasification by-products were obtained from a downdraft biomass gasifier system and were characterized in terms of chemical and physical properties. FTIR analysis confirmed similar spectra in all char-resin blends. For fine carbon particles- (soot-) resin blends, almost the same functional groups as observed in char-resin blends appeared. In bomb calorimeter measurements, 70% resin/30% char blends gave highest calorific value, followed by 50% resin/50% soot blends with values of 35.23 MJ/kg and 34.75 MJ/kg consecutively. Provided these by-products meet certain criteria, they could be used in other areas such as varnishes, water purification, and wind turbine blades
