Photocatalytic degradation of real textile wastewater using carbon black-Nb2O5 composite catalyst under UV/Vis irradiation.

This work investigated the impregnation of Nb2O5 into carbon black (CB) in different ratios and its effect in photocatalytic degradation of real wastewater from a dyeing factory by advanced oxidative processes (AOP). Synthesized catalysts were characterized regarding their crystalline structure (DRX, micro-Raman), morphology (MEV), textural (BET area) and optical properties (bandgap energy by diffuse reflectance) and pH at the point of zero charge (pHpzc). Preliminary tests showed better photodegradation results in the acidic medium after 5 h of irradiation with NCB-0.5 (Nb2O5:CB 0.5:1). Treatment parameters optimization was carried out using response surface methodology based on Box-Behnken experimental design. Catalyst concentration, solution pH and irradiation time were varied, analysing absorbance reduction (285 and 574 nm), COD and TOC removal after treatment as responses. The composite catalyst showed improved photocatalytic activity, attributed to an increase in adsorption capacity and the bandgap narrowing, redshifting the absorption edge wavelength to the visible region, brought by CB impregnation. Optimal conditions were found at 0.250 g L-1 of catalyst, pH 2.0 and 5 h of irradiation, removing 72.19% and 93.52% of absorbance in 285 and 574 nm, respectively, 51.29% of COD and 70.70% of TOC using NCB-0.5.

Coagulation/flocculation of textile effluent using a natural coagulant extracted from Dillenia indica.

The aim of this study was to assess the efficiency of mucilage extracted from the fruit of Dillenia indica for enhancing coagulation in the treatment of textile effluent. The mucilage extraction was carried out in water at room temperature. The pH, concentration of coagulant FeCl3.6H2O, and concentration of mucilage solution were optimized with star-type central composite design (CCD). We were able to analyze the synergistic effects between the FeCl3.6H2O and mucilage concentrations: the process of coagulation/flocculation (CF) for chemical oxygen demand (COD) removal was more efficient at a low chemical coagulant concentration (8.00 mg L-1) and a higher natural coagulant (NC) concentration (15.00 mg L-1). This demonstrated the potential of this mucilage to treat textile effluents, with 67.66%% COD removal, 96.86% turbidity removal and 91.12% apparent color reduction. The characterization of the mucilage of Dillenia indica was done using Fourier transform infrared spectroscopy (FTIR) and solid-state cross-polarization magic angle spinning carbon-13 nuclear magnetic resonance (CP/MAS 13C NMR), and the signals obtained indicated the presence of polysaccharides, which are responsible for enhancing the CF process.

Hydrogen peroxide-assisted photocatalytic degradation of textile wastewater using titanium dioxide and zinc oxide.

The present work investigated the degradation of a dyeing factory effluent by advanced oxidative process under UV irradiation. TiO2 and ZnO were used as catalysts and the influence of different concentrations of H2O2 added to the system was studied. The catalysts were characterized in terms of crystal structure (X-ray diffraction), textural properties (Brunauer-Emmett-Teller area and pore volume) and point of zero charge, which indicated the semiconductors had a positively charged surface in an acidic medium. After 8 h of irradiation at pH 3.0 and catalyst concentration of 0.0625 g L-1, the effect of H2O2 was evaluated by means of kinetic efficiency (rate constants), absorbance reduction (at 284, 621 e 669 nm), total organic carbon reduction and mineralization (in terms of the formation of ions such as NH4+ and NO3- ). Adding H2O2 to the photocatalytic system significantly increased pollutants' removal, highlighting tests with 1.0 × 10-2 mol L-1, showing higher absorbance reduction and rate constants at 621 and 669 nm for TiO2 and best mineralization rates for ZnO. Ecotoxicity bioassays using Artemia salina L confirmed the treatment efficacy, with effluent lethal concentration (LC50) increasing from 65.68% (in natura) to over 100% after photocatalysis treatment.

Combined processes of ozonation and supercritical water oxidation for landfill leachate degradation.

Leachate is a highly variable, heterogeneous and recalcitrant wastewater generated in landfills which may contain high concentrations of many organic and inorganic compounds, hampering the application of a single technique in its treatment. Therefore, this paper assessed leachate degradation through supercritical water oxidation (ScWO) as well as combined processes of ozonation and supercritical water oxidation (O3/ScWO and ScWO/O3), a yet innovative combination. Ozonation was carried out at different reaction times (30-120 min). ScWO was developed at 600 °C, 23 MPa, and spatial time (τ) from 29 to 52 s. A combination of ozonation (30 min) and supercritical water oxidation process (O3-30'/ScWO) was the most efficient technique for the degradation of the leachate assessed. These conditions enabled to remove high values of apparent and true color (92% and 97%, respectively), biochemical oxygen demand (BOD5,20) (95%), chemical oxygen demand (COD) (92%), total organic carbon (TOC) (79%), nitrite (78%), nitrate (84%), total (96%), dissolved (96%) and suspended (94%) solids. In addition, the combined process presented significant decrease in electric conductivity (EC) (68%) and less leachate turbidity removal (43%). Except for ammonia and nitrite, all parameters of the leachate treated by O3-30'/ScWO met the specifications of Brazilian legislation (CONAMA Resolutions No. 357/2005 and No. 430/2011) for the disposal of wastewater in water bodies. Besides, both processes are considered to be clean technologies. This shows the great possibility of applying the O3/ScWO combination to landfills leachates.

The use of a natural coagulant (Opuntia ficus-indica) in the removal for organic materials of textile effluents.

The goal of this study was to investigate the activity of the coagulant extracted from the cactus Opuntia ficus-indica (OFI) in the process of coagulation/flocculation of textile effluents. Preliminary tests of a kaolinite suspension achieved maximum turbidity removal of 95 % using an NaCl extraction solution. Optimization assays were conducted with actual effluents using the response surface methodology (RSM) based on the Box-Behnken experimental design. The responses of the variables FeCl3, dosage, cactus dosage, and pH in the removal of COD and turbidity from both effluents were investigated. The optimum conditions determined for jeans washing laundry effluent were the following: FeCl3 160 mg L(-1), cactus dosage 2.60 mg L(-1), and pH 5.0. For the fabric dyeing effluent, the optimum conditions were the following: FeCl3 640 mg L(-1), cactus dosage 160 mg L(-1), and pH 6.0. Investigation of the effects of the storage time and temperature of the cactus O. ficus-indica showed that coagulation efficiency was not significantly affected for storage at room temperature for up to 4 days.

Toxicity assessment of textile effluents treated by advanced oxidative process (UV/TiO2 and UV/TiO2/H2O2) in the species Artemia salina L.

Textile industry wastes raise a great concern due to their strong coloration and toxicity. The objective of the present work was to characterize the degradation and mineralization of textile effluents by advanced oxidative processes using either TiO(2) or TiO(2)/H(2)O(2) and to monitor the toxicity of the products formed during 6-h irradiation in relation to that of the in natura effluent. The results demonstrated that the TiO(2)/H(2)O(2) association was more efficient in the mineralization of textile effluents than TiO(2), with high mineralized ion concentrations (NH (4) (+) , NO (3) (-) , and SO (4) (2-) ) and significantly decreased organic matter ratios (represented by the chemical oxygen demand and total organic carbon). The toxicity of the degradation products after 4-h irradiation to Artemia salina L. was not significant (below 10 %). However, the TiO(2)/H(2)O(2) association produced more toxicity under irradiation than the TiO(2) system, which was attributed to the increased presence of oxidants in the first group. Comparatively, the photogenerated products of both TiO(2) and the TiO(2)/H(2)O(2) association were less toxic than the in natura effluent.

Optimised photocatalytic degradation of a mixture of azo dyes using a TiO(2)/H(2)O(2)/UV process.

The aim of the present study was to optimise the photocatalytic degradation of a mixture of six commercial azo dyes, by exposure to UV radiation in an aqueous solution containing TiO(2)-P25. Response surface methodology, based on a 3(2) full factorial experimental design with three replicates was employed for process optimisation with respect to two parameters: TiO(2) (0.1-0.9 g/L) and H(2)O(2) (1-100 mmol/L). The optimum conditions for photocatalytic degradation were achieved at concentrations of 0.5 g TiO(2)/L and 50 mmol H(2)O(2)/L, respectively. Dye mineralisation was confirmed by monitoring TOC, conductivity, sulfate and nitrate ions, with a sulfate ion yield of 96% under optimal reactor conditions. Complete decolorisation was attained after 240 min irradiation time for all tested azo-dyes, in a process which followed a pseudo-first kinetic order model, with a kinetic rate constant of approximately 0.018 min(-1). Based on these results, this photocatalytic process has promise as an alternative for the treatment of textile effluents.

Combined electrocoagulation and TiO(2) photoassisted treatment applied to wastewater effluents from pharmaceutical and cosmetic industries.

The treated wastewater consists of refractory materials and high organic content of hydrolyzed peptone residues from pharmaceutical factory. The combination of electrocoagulation (EC) followed by heterogeneous photocatalysis (TiO(2)) conditions was maximized. The EC: iron cathode/anode (12.50 cmx2.50 cmx0.10 cm), current density 763Am(-2), 90min and initial pH 6.0. As EC consequence, the majority of the dissolved organic and suspended material was removed (about 91% and 86% of the turbidity and chemical oxygen demand (COD), respectively). After EC, refractory residues still remained in the effluent. The subsequent photocatalysis: UV/TiO(2)/H(2)O(2) (mercury lamps), pH 3.0, 4h irradiation, 0.25gL(-1) TiO(2) and 10mmolL(-1) H(2)O(2) shows high levels of inorganic and organic compounds eliminations. The obtained COD values: 1753mgL(-1) for the sample from the factory, 160mgL(-1) after EC and 50mgL(-1) after EC/photocatalyzed effluents pointed out that the combined treatment stresses this water purification.

The effect of operational parameters on electrocoagulation-flotation process followed by photocatalysis applied to the decontamination of water effluents from cellulose and paper factories.

Cellulose and paper pulp factories utilize a large amount of water generating several undesirable contaminants. The present work is a preliminary investigation that associates the electrocoagulation-flotation (EC) method followed by photocatalysis to treat such wastewater. For EC, the experiment with aluminium and iron electrodes showed similar efficiency. Iron electrodes (anode and cathode) were chosen. By applying 30min of EC/Fe(0), 153A m(-2) and pH 6.0, the COD values, UV-vis absorbance and turbidity underwent an intense decrease. For the subsequent UV photocatalysis (mercury lamps) TiO(2) was employed and the favourable operational conditions found were 0.25g L(-1) of the catalyst and solution pH 3.0. The addition of hydrogen peroxide (50mmol L(-1)) highly increased the photo-process performance. By employing the UV/TiO(2)/H(2)O(2) system, the COD reduction was 88% compared to pre-treated effluents and complete sample photobleaching was verified. The salt concentration on EC (iron electrodes) showed that the electrolysis duration can be reduced from 30 to 10min by the addition of 5.0g L(-1) of NaCl. The biodegradability index (BOD/COD) increased from 0.15 (pre-treated) to 0.48 (after EC) and to 0.89 (after EC/photocatalysis irradiated for 6h), showing that the employed sequence is very helpful to improve the water quality. This result was confirmed by biotoxicity tests performed with microcrustaceous Artemia salina.