RESUMO
The potentials of mesoporous TiO2-ZnO (3TiZn) were explored on photocatalytic degradation of doxycycline (DOX) antibiotic, likewise the influence of adsorption on the photocatalytic process. The 3TiZn was characterized for physical and chemical properties. Stability, reusability, kinetic and the ability of 3TiZn to degrade high concentration of pollutant under different operating conditions were investigated. Photocatalytic degradation of DOX was conducted at varied operating conditions, and the best was obtained at 1 g/L catalyst dosage, solution inherent pH (4.4) and 50 ppm of DOX. Complete degradation of 50 ppm and 100 ppm of DOX were attained within 30 and 100 min of the reaction time, respectively. The stability and reusability study of the photocatalyst proved that at the tenth (10th) cycle, the 3TiZn is as effective in the degradation of DOX as in the first cycle. This may be attributed to the fusion of the mixed oxides during calcination. The 3TiZn is mesoporous with a pore diameter of 17 nm, and this boosts it potential to degrade high concentration of DOX. It was observed that the adsorption capacity of 3TiZn enhance the photocatalytic process. It can be emphasized that 3TiZn portrayed a remarkable catalyst stability and good potentials for industrial application.
RESUMO
The refinery industry has witnessed tremendous activity aimed at producing petrochemicals for the benefit of the teeming populace. These activities are accompanied by the discharge of wastewater containing chemical substances and elements that have negative impacts on the ecosystem. The presence of phenol and cyanide contaminants in refinery wastewater poses serious health hazards to humans, necessitating their removal. In this study, boron oxide-doped multi-walled carbon nanotubes (B2O3/MWCNTs) and titanium boride-doped MWCNT (TiB/MWCNTs) nanoadsorbents were prepared via a wet impregnation method and characterized using High-Resolution Transmission Electron Microscopy (HR-TEM), X-Ray Diffraction (XRD), and X-ray Photoelectron Spectroscopy (XPS). HR-TEM images depict the nanostructure of the nanoadsorbent, the presence of doped materials, and the internal, external, and wall thickness of B2O3/MWCNTs and TiB/MWCNTs nanoadsorbents. XRD results indicate that the nanomaterials were monocrystalline with average crystallite sizes of 22.75 nm and 16.79 nm for B2O3/MWCNTs and TiB/MWCNTs, respectively. The formation of B2O3 and TiB was observable in the results obtained from the XPS at the binding energy of 192 and 193.1 eV, respectively. The application of the produced B2O3/MWCNTs and TiB/MWCNTs nanoadsorbents for the removal of phenol and cyanide from refinery wastewater was explored in a batch adsorption system. The effects of contact time, adsorbent dosage, and adsorption temperature were investigated. To the best of our knowledge, the incorporation of B2O3 and TiB in MWCNTs resulted in the highest adsorption capacities for phenol and cyanide from aqueous solutions. The highest percentage removal of 100% for phenol and 99.06% for cyanide was observed for the TiB/MWCNTs nanoadsorbent at a residence time of 70 minutes, a temperature of 60 °C, and 0.3 g of adsorbent. The isotherm models show that cyanide and phenol removal obeyed the Langmuir isotherm, indicating monolayer adsorption over B2O3/MWCNTs nanoadsorbent. Furthermore, cyanide and phenol removal depict multilayer adsorption on the TiB/MWCNT nanoadsorbent. The research shows that B2O3/MWCNTs are proficient in cyanide sorption, while TiB/MWCNT favors phenol sorption due to their respective adsorption capacities.
RESUMO
The presence of As(V) and Mn(VII) in water beyond the permissible concentration allowed by World Health Organization (WHO) standard affects human beings, animals and the environment adversely. Hence, there is need for an efficient material to remove these potentially toxic elements from wastewater prior to discharge into water bodies. This research focused on the application of response surface method (RSM) assisted optimization of Fe-Ni/Activated carbon (AC) catalyst for the synthesis of MWCNTs. Also, the MWCNTs was carboxylated and the adsorption behaviors of both nano-adsorbents in the removal of As(V) and Mn(VII) from industrial wastewater was investigated through experimental and computational techniques. The prepared Fe-Ni/AC, MWCNTs and MWCNTs-OCH2CO2H were characterized using BET, TGA, FTIR, HRSEM, HRTEM, XRD and XPS. The result showed the BET surface area of Fe-Ni/AC, MWCNTs and MWCNTs-OCH2CO2H were obtained as 1100, 1250 and 1172 m2/g, respectively. Due to the enhanced impact of carboxylation, the adsorption capacity of As(V) and Mn(VII) removal increased from 200 to 192 mg/g for MWCNTs to 250 and 298 mg/g for MWCNTs-OCH2CO2H. The isotherm and kinetic models were best fitted by Langmuir and pseudo-second order kinetics, while the thermodynamic investigation found that the adsorption process was endothermic, spontaneous and chemisorptions controlled. The regeneration potential of MWCNTs and MWCNTs-OCH2CO2H after six repeated applications revealed good stability of adsorption efficiency. The study demonstrated optimization importance of Fe-Ni/AC catalyst design for MWCNTs adsorbents and the potentials of utilizing both MWCNTs and MWCNTs-OCH2CO2H in the removal of selected heavy metals from water and soil.