Electrochemical synthesis and characterization of basic bismuth nitrate [Bi6O5(OH)3](NO3)5·2H2O: a potential highly efficient sorbent for textile reactive dye removal

A new method of synthesis was developed for the preparation of basic bismuth nitrate [Bi6O5(OH)3](NO3)5·2H2O (ECBBN). Electrochemical synthesis of the material was carried out by galvanostatic electrodeposition from an acidic Bi(III) solution on a Ti substrate and further thermal treatment in air at 200 °C. Characterization of ECBBN was conducted by employing SEM–EDX, N2 adsorption, XRD and FTIR, and its pI was also determined. The analyses showed that the material obtained was pure [Bi6O5(OH)3](NO3)5·2H2O. Morphologically, ECBBN aggregates were composed of crystals, some smaller than 50 nm. Electrochemically synthesized sorbent (ECBBN) was used for the removal of the textile dye Reactive Blue 19 (RB19) from deionized water and model solutions of polluted river water, and it showed considerably superior sorption performance compared to other inorganic sorbents synthesized by conventional methods reported in the literature. A kinetic study suggests that the sorption process is both under reaction and diffusion control. Equilibration of the sorption process was attained in several minutes, i.e. the sorption process is very fast. The sorption equilibrium data were well interpreted by the Langmuir, Redlich–Peterson and Brouers–Sotolongo isotherm. Using Langmuir isotherm, the maximum sorption capacity of ECBBN was reached at pH 2 and was 1049.19 mg g−1

New Way of Synthesis of Basic Bismuth Nitrate by Electrodeposition from Ethanol Solution: Characterization and Application for Removal of RB19 from Water

A new method of synthesis was developed for the preparation of sorbent basic bismuth nitrate [Bi6O5(OH)(3)](NO3)(5)center dot 2H(2)O (BBN-EtOH). This electrochemical method includes electrodeposition from an acidic Bi(III) solution in 96% ethanol at a constant current density of 150.0 mA cm(-2). Final product was obtained by thermal treatment at 200 degrees C. Characterization of BBN-EtOH was conducted by employing XRD, FTIR, SEM-EDX as well as BET, and its pI was also determined. The analysis showed that the material obtained is pure [Bi6O5(OH)(3)](NO3)(5)center dot 2H(2)O. Morphologically, it is composed of aggregates which were formed of several smaller particles of various shapes and sizes, some smaller than 100 nm. Electrochemically synthesized sorbent (BBN-EtOH) was used for the removal of the textile dye Reactive Blue 19 (RB19) from deionized water and model solution of river water, and it showed considerably superior sorption performance compared to other inorganic sorbents synthesized by conventional methods reported in the literature. Kinetic study suggests that the sorption process is both under reaction and diffusion control. Equilibrium of the sorption process was attained in several minutes, i.e., the sorption process is very fast. The sorption equilibrium data were well interpreted by the Langmuir, Sips and Brouers-Sotolongo isotherm. The maximum sorption performance was achieved at pH 2.0, and according to the Langmuir isotherm, it is 1344.99 mg g(-1)

Electrochemically synthesized Molybdenum oxides for enhancement of atmospheric pressure non-thermal pulsating corona plasma induced degradation of an organic compound

MoO2 and MoO3 were applied as catalysts for plasma degradation of organic compound. They were prepared by electrodeposition (MoO2) and electrodeposition followed by thermal treatment (MoO3), and then characterized by the cyclic voltammetry, SEM, EDX, XRD, and FTIR. The RB 19 was degraded by self-made non-thermal atmospheric pressure pulsating plasma corona reactor. Decolourization mechanism, parameters, kinetics, and influence of the catalysts were examined. Mo-oxides enhanced degradation reactions rate constants by 45% – 50%, increased decolourization rate at all the tested pHs, discharged current densities, and decreased energy consumption. Degradation followed the pseudo-first kinetics order and proceeded via plasma-generated ⋅OH radical, which attacked dye molecule; MoO2 and MoO3, excited by plasma-generated UV radiation and high-energy chemical species bombardment, enhanced decomposition of plasma-generated H2O2 into ⋅OH radicals, thus enhancing production of degradation agent. Higher percentage of mineralization was attained in the presence of catalysts, which maintained their degradation activity after 5 uses

A New Photocatalyst Bismuth Oxo Citrate: Synthesis, Characterization, and Photocatalytic Performance

A new photocatalyst bismuth oxo citrate was synthesized by facile precipitation process with calcination at 200 8C. The photocatalyst was characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), Fouriertransform infrared (FTIR) spectroscopy, N2 sorptometry, and elemental analysis. Morphologically, it is composed of polyhedral particles with different, irregular shapes and sizes. The specific surface area (SSA) of the photocatalyst was 8.92 m2 g-1. It showed very good photocatalytic performance and reusability. Total decolorization of Reactive Blue 19 (RB19) was achieved in less than 10 minutes, which is much faster in comparison with TiO2 P25. Also, bismuth oxo citrate showed higher photocatalytic activity than other photocatalysts based on bismuth compounds reported by other authors. Optimal photocatalysis parameters were pH 2 and photocatalyst dose of 250 mg dm-3. The decolorization rate was found to decrease as initial dye concentration increased. The photocatalytic data best fitted to L-H kinetic model with pseudo-first order reaction rate. Chrastil diffusion model showed that diffusion has not influence on the process. Water Environ. Res., 90, 719 (2018). © 2018 Water Environment Federation

Heterogeneous photocatalytic degradation of anthraquinone dye Reactive Blue 19: optimization, comparison between processes and identification of intermediate products

Treatment of textile wastewater using heterogeneous photocatalysis began in the the last decade and attracted the attention of researchers due to its versatile application. The variety of applications of TiO2 as a photocatalyst was due toits numerous positive properties, such as low operating temperature, biologically inert nature, low energy consumption, water insolubility, availability and photoactivity, low toxicity, high chemical stability, suitable flat band potential, narrow bandgap and the fact that it is environmentally benign. Heterogeneous UV-TiO2 photocatalysis is capable of removing organic pollutants from textile wastewater; this has been widely studied, with the technology also having been commercialized in many developing countries. Decolorization of anthraquinone dye Reactive Blue 19 (RB 19) by heterogeneous advanced oxidation processes TiO2/UV/H2O2, TiO2/UV/KBrO3 and TiO2/UV/(NH4)2S2O8 was studied under different conditions and in the presence of electron acceptors such as hydrogen peroxide (H2O2), potassium bromate (KBrO3) and ammonium persulphate ((NH4)2S2O8). Decolorization was very fast for all three processes, and complete dye decolorization was achieved in 10 min. The effect of various ions (Cl–, SO42– and HCO3–) on RB 19 decolorization was also studied. The optimal condition for the decolorization of the dye were determined to be: TiO2 concentration 1 g∙dm–3, electron acceptor concentration 30.0 mmol∙dm–3, dye concentration 50.0 mg∙dm–3, UV intensity 1 950 μW∙cm–2, at temperature 25 ± 0.5°C. In addition, experiments were performed and compared in three different matrices. In the surface water and dyebath effluent water, the removal efficiency for RB 19 was lower than that achieved in the deionized water because of the interference of complex constituents in the surface water and effluent. LC-MS analysis was carried out and the detected intermediates were compared with the previously published data for anthraquinone dyes