Synergetic adsorption-photocatalysis process for water treatment using TiO2 supported on waste stainless steel slag.

This study presents an economical and efficient method to decolourise dye wastewater using industrial waste stainless steel slag (SSS). Titanium dioxide was immobilised on SSS by a precipitation-calcination method. Samples with different TiO2 loadings (prepared using either titanium isopropoxide precursor or commercial TiO2 nanoparticles) were used to decolourise an organic contaminant (methylene blue) under dark and UV conditions in aqueous solution, and their adsorption and photocatalytic performances were compared. Samples with 15 and 25 TiO2 wt% prepared by the precursor method had normalised photocatalytic efficiencies per gram close to that of bare TiO2; using an adsorption-photocatalysis process led to efficiencies 4.4 and 1.6 times higher than that of pure TiO2. The improvement in catalytic performance (greater for samples with less than 50% TiO2 content) may be due to better UV absorption ability (related to with the improvement of TiO2 particle dispersion) and the close TiO2 support interaction, which can eventually cause a photocatalysis-enhancing shift towards more negative oxidation potentials. The SSS also acted as an efficient adsorption trap for organic compounds. The pollutant was thus transferred to the TiO2 surface and photodegraded more rapidly and efficiently. The outstanding synergetic adsorption-photocatalysis capacities of TiO2 waste stainless steel slag composites for dye water treatment made the proposed conversion approach have great potential in practical applications.

High-capacity adsorbents from stainless steel slag for the control of dye pollutants in water.

Adsorbent materials for the control of dye pollutants in water were synthetized from stainless steel slag (SSS) using different acid-base treatments. Using HCl (SS-Cl) and HNO3 (SS-NO3) produced high-capacity adsorbents, with BET areas of 232 m2/g and 110 m2/g respectively. Specifically, the SS-Cl had a structure of amorphous silica sponge. Treatment with H2SO4 (SS-SO4) did not enhance the adsorption capabilities with respect to the raw sample (SSS). Activated carbon (AC) was also tested as reference. The materials were characterized by X-ray diffraction (XRD), X-ray fluorescence (XRF), N2 adsorption-desorption isotherms, scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDX) zeta potential, and infrared spectroscopy (FTIR). Batch adsorption experiments with methylene blue (MB) showed that the maximum sorption capacities were 9.35 mg/g and 8.97 mg/g for SS-Cl and SS-NO3 at 240 h, respectively. These values, even at slower rate, were close to the adsorption capacity of the AC (9.72 mg/g). This behavior has been attributed to the high porosity in the range of nanopores (0.6-300 nm) and the high-surface area for both samples. Preferential involvement of certain functional groups in the adsorption of dye ions on their surface indicative of chemisorption has been found. Although optimization, repeatability, and reproducibility of the process and environmental assessment have to be done before practical applications, these preliminary results indicate that application of these cost-effective adsorbents from raw SSS may be used in water pollution treatment and contribute to the sustainable development of the steel manufacturing industry.

Photocatalytic Activity of Zn x Mn3-x O4 Oxides and ZnO Prepared From Spent Alkaline Batteries.

Oxides with Zn x Mn3-xO4 stoichiometries and ZnO were synthesized from the "black mass" material recovered from spent alkaline batteries. The oxides were characterized by XRF, XRD with Rietveld refinement, SEM, and TEM methods. Optical characterization included diffuse reflectance (DRS) and photoluminescence (PL) measurements. ZnO presented a clear band edge in the UV region, and PL signals were detected. The Zn/Mn oxides showed strong absorption in the UV region and a continuous absorption band in the Vis-IR regions. There is a non-detected PL signal due to excited charges being trapped on sub-band energy states and/or transfer by non-radiative paths. Photocatalytic activity under both irradiation conditions was evaluated using the resazurin dye test, terephthalic acid fluorescence probe method, and NOx air purification evaluation. In the three photoactivity tests, ZnO performed well under both UV and Vis irradiation, whereas no evidence of any appreciable photocatalytic activity was observed for the Zn/Mn oxides. The results are discussed in terms of the findings of previously reported optical measurements.