This paper reveals the influence of doping on the morphological, structural, and optical properties of zinc oxide (ZnO) nanoparticles (NPs) synthesized by pneumatic spray pyrolysis technique (PSP), using zinc ethoxide ZnO2CH32 as the precursor. The prepared samples were characterized by XRD, HRTEM, SEM-EDX, UV-Vis spectroscopy, and RS. RS analysis has revealed that the unmodified ZnO and carbon modified ZnO samples have characteristic Raman optic modes at 325 cm−1, 373 cm−1, and 432 cm−1 belonging to Wurtzite ZnO structure. The XRD ZnO (C:ZnO) NPS have characteristic peaks of hexagonal Wurtzite ZnO structure. HRTEM analysis has revealed that the synthesized ZnO NPs have particle size range of 8.8–11.82 nm. EDX spectra of both unmodified and modified ZnO nanoparticles have revealed prominent peaks at 0.51 keV, 1.01 keV, 1.49 keV, 8.87 keV, and 9.86 keV. The occurrence of these peaks in the EDX spectra endorses the existence of Zn and O atoms in the PSP synthesized ZnO NPs. The UV-Vis spectroscopy has revealed a red shift of the absorption edge, with the increase in C dopant level. The effect of nanocrystallite size and the gradual prominence of C into ZnO matrix due to increase in C dopant level in the PSP synthesized ZnO NPs was meticulously elaborated through Raman spectroscopy analysis.

Gasification is a promising technology for the production of gaseous fuels, mainly syngas, which is produced from the hydrocarbon-based materials such as coal and biomass. Currently, coal is the main feedstock that is used for the gasification process due to its large reserves and higher energy per volume. However, the use of coal has been a more concern because of the environmental impacts caused by the emission of toxic gases such as the sulphides, sulphates and nitrates as well as the ash slagging problems forming inside the gasifier. On the other hand, biomass is a renewable energy resource of interest as a replacement for coal to reduce the environmental impacts associated with fossil fuel usage. Much consumption of fossil fuels has caused serious energy crisis and environmental impacts, globally. Co-gasification of coal and biomass is considered as a connection between energy production based on fossil fuels and energy production based on renewable fuels. The utilization of biomass by co-gasification with coal causes reductions of carbon dioxide, nitrogen and sulfur emissions due to the renewable character of biomass and low contamination content in biomass. This study determined the properties of various biomass/coal blends and their suitability for co-gasification in a downdraft biomass gasifier. A bomb calorimeter was used to determine the calorific values of the material. CHNS and XRF analysis were carried out to determine the elemental analysis of the material. Thermogravimetric analysis (TGA) was conducted to investigate the thermal degradation of the material. The kinetic analysis of the various feedstocks allows the prediction of the rate at which co-gasification takes place. The results suggested that blending coal with biomass result in a faster reaction rate at lower temperatures than that of coal alone and lower activation energy due to the high quantity of volatile matter in biomass.

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% ZnCl 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.

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 Fe, Cr, Cu, Ni and Pb 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 Fe, Ni and Cr. 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.

photodegradation of bentazon. A bentazon removal efficiency of 90.1 % was achieved at pH 7. N-TiO 2 -PMAAg-PVDF/PAN membranes were successfully prepared and characterized. These photocatalytic membranes showed great potential as a technology for the effective removal of pesticides from water. According to literature, N-TiO 2 -PMAA-g-PVDF/PAN asymmetric photocatalytic membranes have not been prepared before for the purpose of treating agricultural wastewater.

This work investigates the preparation of a magnetically recoverable photocatalytic nanocomposite of maghemite nanoparticles coated with silica and carbon doped titanium dioxide. The novel nanocomposite boasts the advantages of efficient photocatalytic degradation of organic pollutants in water and ease of recovery of the fine particles after water treatment. The photocatalytic nanocomposite was successfully synthesized through a stepwise approach via co-precipitation and sol-gel methods. Characterisation by Fourier transform infrared (FTIR), X-ray diffraction (XRD), transmission electron microscopy (TEM) and energy dispersive spectroscopy (EDS) substantiated the existence of the intended structure of the nanocomposite and the particles were found to be in the size range of 15–22 nm with a quasi-spherical shape. Brunauer–Emmett–Teller (BET) surface area analysis revealed an average surface area of 55.20 m2/g, which is higher than that of commercial TiO2 (Degussa P25, 50.00 m2/g), and an average pore diameter of 8.36 nm. A 5 ppm methylene blue solution was degraded with an efficiency of 96.8% after 3 h of solar irradiation, which was 19.7% greater than using the same photo-catalyst under strict UV light irradiation. Photo-catalysis using these nanoparticles was observed to be very effective. The prepared novel visible light active nanocomposite has great potential for incorporation into water treatment systems because it exhibits good stability and magnetism, as well as high photocatalytic efficiency.

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 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.