Efficient microbial cellulose/Fe3O4 nanocomposite for photocatalytic degradation by advanced oxidation process of textile dyes.

Fenton-type advanced oxidative processes (AOP) have been employed to treat textile dyes in aqueous solution and industrial effluent. The work focused on assisting the limitations still presented by the Fenton process regarding the use of suspended iron catalysts. Soon, a nanocomposite of bacterial cellulose (BC) and magnetite (Fe3O4) was developed. It has proven to be superior to those available in the literature, exhibiting purely catalytic properties and high reusability. Its successful production was verified through analytical characterization, while its catalytic potential was investigated in the treatment of different textile matrices. In initial tests, the photo-Fenton process irradiated and catalyzed by sunlight and BC/Fe3O4 discolored 92.19% of an aqueous mixture of four textile dyes. To improve the efficiency, the design of experiments technique evaluated the influence of the variables pH, [H2O2], and the number of BC/Fe3O4 membranes. 99.82% of degradation was obtained under optimized conditions using pH 5, 150 mg L-1 of H2O2, and 11 composite membranes. Reaction kinetics followed a pseudo-first-order model, effectively reducing the organic matter (COD = 83.24% and BOD = 88.13%). The composite showed low iron leaching (1.60 ± 0.08 mg L-1) and high stability. It was recovered and reused for 15 consecutive cycles, keeping the treatment efficiency at over 90%. As for the industrial wastewater, the photo-Fenton/sunlight/BC/Fe3O4 system showed better results when combined with the physical-chemical coagulation/flocculation process previously used in the industry's WWTP. Together they reduced COD by 77.77%, also meeting the color standards (DFZ scale) for the wavelengths of 476 nm (<3 m-1), 525 nm (<5 m-1), and 620 nm (<7 m-1). Thus, the results obtained demonstrated that employing the BC/Fe3O4 composite as an iron catalyst is a suitable alternative to materials employed in suspension. This is mainly due to the high catalytic activity and power of reuse, which will reduce treatment costs.

Original nanostructured bacterial cellulose/pyrite composite: Photocatalytic application in advanced oxidation processes.

The development of an original catalytic composite of bacterial cellulose (BC) and pyrite (FeS2) for environmental application was the objective of this study. Nanoparticles of the FeS2 were synthesized from the hydrothermal method and immobilized on the BC structure using ex situ methodology. In the BC, the FTIR and XRD analyzes showed the absorption band associated with the Fe-S bond and crystalline peaks attributed to the pyrite. Thus, the immobilization of the iron particles on the biopolymer was proven, producing the composite BC/FeS2. The use of the SEM technique also ratifies the composite production by identifying the fibrillar structure morphology of the cellulose covered by FeS2 particles. The total iron concentration was 54.76 ± 1.69 mg L-1, determined by flame atomic absorption analysis. TG analysis and degradation tests showed respectively the thermal stability of the new material and its high catalytic potential. A multi-component solution of textile dyes was used as the matrix to be treated via advanced oxidative processes. The composite acted as the catalyst for the Fenton and photo-Fenton processes, with degradations of 52.87 and 96.82%, respectively. The material proved stability by showing low iron leaching (2.02 ± 0.09 and 2.11 ± 0.11 mg L-1 for the respective processes). Thus, its high potential for reuse is presumed, given the remaining concentration of this metal in the BC. The results showed that the BC/FeS2 composite is suitable to solve the problems associated with using catalysts in suspension form.

Treatment of textile matrices using Fenton processes: influence of operational parameters on degradation kinetics, ecotoxicity evaluation and application in real wastewater.

Since conventional processes for treating textile effluents have limitations, this work aimed to investigate the application of advanced oxidation technology in this type of matrix. Initially, for a textile dyes mixture in solution, the photo-Fenton/sunlight process proved to be the most efficient among other systems tested. During the tests it was found that the degradation kinetics depends of the pH and catalyst and oxidant concentrations. After 60 min under optimized conditions, the color was reduced by 98.19%, with 92.52% organic matter conversion. Ecotoxicity tests with the Lactuca Sativa vegetable indicated that the dyes were not totally oxidized to inert compounds, although the treated solution did not cause a significant toxic effect for this species. In the second stage of the research, the photodegradation in real samples of textile wastewater was evaluated. The efficiency of the photo-Fenton/sunlight process was lower than that obtained for the dyes solution, a fact attributed to the greater complexity of the real matrix. However, the data also indicated that the combination of coagulation/flocculation and advanced oxidation processes is the most suitable methodology to reduce the fraction of biodegradable compounds. In summary, research has revealed that photocatalytic degradation of dyes through advanced oxidation is an efficient treatment.

Degradation of the residual textile mixture cetyltrimethylammonium bromide/remazol yellow gold RNL-150%/reactive blue BF-5G: evaluation photo-peroxidation and photo-Fenton processes in LED and UV-C photoreactors.

This article presents a study on the degradation of a residual textile mixture composed of cationic surfactant cetyltrimethylammonium bromide (CTAB) and the remazol yellow gold RNL-150% and reactive blue BF-5G textile dyes. This was carried out by employing the photo-peroxidation and photo-Fenton processes in LED and UV-C photoreactors. The photo-Fenton process was the most efficient as regards the degradation of the CTAB and dye mixture, for both types of radiation. In the kinetic study, degradations of 99% were obtained in 180 min for the chromophore groups using both types of radiation. The degradation of the CTAB and aromatic groups was, meanwhile, an average of 25% when employing LED radiation. The behavior of the degradation reaction was pseudo-first-order. Toxicity tests indicated that the solutions were better able to grow seeds and bacteria after treatment with the photo-Fenton process, using both types of radiation. The photo-Fenton processes carried out by employing LED and UV-C photoreactors were able to degrade the CTAB and dye mixture, thus highlighting the efficiency of LED radiation when its power (three times smaller) is compared to that of UV-C radiation. This process, therefore, represents an alternative for use in textile wastewater treatment systems.

Investigation of paracetamol degradation using LED and UV-C photo-reactors.

This work investigates the efficiency of LED and UV-C photo-reactors for paracetamol degradation using advanced oxidative processes. Among the evaluated processes, photo-Fenton was the most efficient for both radiations. Degradations greater than 81% (λ 197 nm) and 91% (λ 243 nm) were obtained in the kinetic study. These degradations were also observed by means of the reduction in the peaks in both spectral scanning and high-performance liquid chromatography analysis. The good fit of the Chan and Chu kinetic model shows that the degradation reaction has pseudo-first order behavior. Toxicity tests did not indicate the inhibition of growth of Lactuca sativa seeds and Escherichia coli bacterium. However, the growth of strains of the Salmonella enteritidis bacterium was inhibited in all the samples, demonstrating that only this bacterium was sensitive to solutions. The proposed empirical models obtained from the 24 factorial designs were able to predict paracetamol degradation. These models could, at the same levels assessed, be used to predict the percentage of degradation in studies using other organic compounds. The LED and UV-C photo-reactors were, when employing the photo-Fenton process, able to degrade paracetamol, thus highlighting the efficiency of LED radiation when its power (three times smaller) is compared to that of UV-C radiation.

Kinetic study of dye removal using TiO2 supported on polyethylene terephthalate by advanced oxidation processes through neural networks.

This work investigated the efficiency of polyethylene terephthalate (PET) as support material for TiO2 films in the photocatalytic degradation of red Bordeaux and yellow tartrazine dyes. The optimum operating conditions were determined by a factorial design, which resulted after 180 min of treatment in degradations of 99.5% and 99.1% for the UVC/H2O2/TiO2Sup and solar/H2O2/TiO2Sup systems, respectively. For the kinetic study, the experimental data fitted to the pseudo-first-order model and the calculated kinetic constants (k) values were 0.03 min-1 for the UVC/H2O2/TiO2Sup system and 0.0213 min-1 for the system solar/H2O2/TiO2Sup. It was verified that TiO2 supported in the PET remained with high degradation efficiency even after five cycles of reuse, indicating a good stability of the photocatalyst in the support. A significant reduction of TOC content was also observed along the reaction time. The phytotoxicity bioassay with Lactuca sativa demonstrated that after treatment with UVC/H2O2/TiO2Sup and solar/H2O2/TiO2SUP, an increase in IC50 and consequently lower toxicity was observed.

Use of TiO2 photocatalyst supported on residues of polystyrene packaging and its applicability on the removal of food dyes.

This work proposes the use of plastic residues, more specifically polystyrene packaging, to support TiO2, used as a photocatalyst in the degradation of erythrosine and Brilliant Blue food dyes. The scanning electron microscopy and Fourier transform infrared spectroscopy analyses exhibited the surface coating and the presence of TiO2 in the material, respectively. The UV/H2O2/TiO2 ((SP)supported) process was used in the preliminary study, given the high percentage of degradation, operational advantages and greater reductions in peaks related to the aromatic rings when compared to the other processes studied. For the factorial design, the highest efficiency was reached for 150 mg of TiO2, a H2O2 concentration of 11.2 mmol L-1 and pH of 5.0. These conditions were used in the degradation kinetics, which was rapid during the first 30 min, with the concentration of dyes in the solution reaching values close to zero after 180 min. Based on the mechanism proposed, the pseudo-first order kinetic model presented the best adjustment to the experimental data. After treatment, the solution presented greater biodegradability and lower toxicity, verified by the lettuce seed germination test (Lactuca sativa). Thus, the UV/H2O2/TiO2((SP)supported) process showed great potential in the treatment of industrial effluents contaminated by these food dyes, as well as in reusing discarded polystyrene packaging to support the photocatalyst.

Application of the advanced oxidative process on the degradation of the green leaf and purple açaí food dyes with kinetic monitoring and artificial neural network modelling.

The study evaluated the advanced oxidative processes concerning the degradation of green leaf and purple açaí dyes, as well as the prediction of data through artificial neural networks (ANNs). It was verified that percentage of degradation on the wavelengths (λ) of 215, 248, 523 and 627 nm was 5.95, 49.99, 98.17 and 95.99%, respectively, when UV/H2O2 action and UV-C radiation was applied. A non-linear kinetic model proposed by Chan and Chu presented a good fit to the experimental data, reaching an R2 value between 0.978 and 0.999, for the studied λ. Within the ANN simulations through Statistica 6.0, the multilayer perceptron (MLP) (3-9-4) presented a better fit to the experimental data. However, higher values of R² were obtained when utilizing the sklearn package with Python language and an MLP (4-5-4) model. Assays with Staphylococcus aureus and Staphylococcus pyogenes bacteria isolates were performed and it was verified that after employing the UV/H2O2 process, there was a decrease in the toxicity of the solution of dyes. In evaluating S. aureus toxicity, normal growth was observed. However, for S. pyogenes bacteria, it was found that when using the UV/H2O2 process, toxicity was evidenced at post-treatment solution concentrations of 100, 70 and 50%.

Degradation of textile dyes Remazol Yellow Gold and reactive Turquoise: optimization, toxicity and modeling by artificial neural networks.

In this work, the degradation of Remazol Yellow Gold RNL-150% and Reactive Turquoise Q-G125 were investigated using AOP: photolysis, UV/H2O2, Fenton and photo-Fenton. It was found that the photo-Fenton process employing sunlight radiation was the most efficient, obtaining percentages of degradation above 87%. The ideal conditions for the degradation of the dyes were determined from a factorial design 23 and study of the [H2O2] ([H2O2] equal to 100 mg·L-1); [Fe] equal to 1 mg·L-1 and pH between 3 and 4. In the kinetic study, a degradation of more than 97% was obtained after 150 min for the chromophoric groups and 91% for the aromatic compounds. The experimental data obtained presented a good fit to the nonlinear kinetic model. The model of artificial neural networks multilayer perceptron (MLP) (4-11-5) using the software Statistica 8.0 enabled the modeling of the degradation process and showed a better prediction of the data. The toxicity to the seeds of Lactuca sativa and the bacteria Escherichia coli and Salmonella enteritidis allowed to evaluate the effectiveness of the process. The results of this study suggest that the use of photo-Fenton process with sunlight radiation is an effective way to degrade the dyes under study.

Adsorption of azo dyes using peanut hull and orange peel: a comparative study.

This work proposes the use of agro-industrial wastes, specifically peanut hull (HP) and orange peel (OP), as adsorbents for dyes, such as Remazol Golden Yellow RNL-150% (RYG), Gray Reactive BF-2R (RG) and Reactive Turquoise Q-G125 (RT). Characterization by Brunauer-Emmett-Teller indicates that the adsorbents are mesoporous, with pHzpc values of 5.0 for HP and 4.0 for OP. Fourier transform-infrared spectroscopy identified carbonyl and sulphonic groups. The initial pH of the best-adsorbing solution of the three colours was 2.0. Increasing the concentration of the adsorbent promoted an increase in the percentage of removal until saturation of the adsorbent. In a factorial design, the largest value of q was obtained with 0.25 g of the adsorbent, with a particle size of < 0.4 mm and a stirring speed of 300 rpm. Such conditions were used in kinetic studies and studies of adsorption equilibrium. The evolution kinetics were rapid in the first few minutes, and after 180 min the system reached equilibrium. The kinetic model that best fit the experimental data to a 95% confidence level for the F test was the pseudo-second-order model for RYG/HP, RG/OP and RT/OP. There was no significant difference between the kinetic models as evaluated by the F test for RYG/OP, RG/HP and RT/HP. The experimental results indicated favourable dye adsorption characteristics for the adsorbents studied. The results of the F test showed that for RYG and RG, there was no significant difference between the two evaluated models. This study suggests that HP and OP are viable alternatives for the treatment of effluents containing RYG, RG and RT dyes.