Bionanomining of copper-based nanoparticles using pre-processed mine tailings as the precursor.

The bacterial synthesis of copper nanoparticles emerges as an eco-friendly alternative to conventional techniques since it comprises a single-step and bottom-up approach, which leads to stable metal nanoparticles. In this paper, we studied the biosynthesis of Cu-based nanoparticles by Rhodococcus erythropolis ATCC4277 using a pre-processed mining tailing as a precursor. The influence of pulp density and stirring rate on particle size was evaluated using a factor-at-time experimental design. The experiments were carried out in a stirred tank bioreactor for 24 h at 25 °C, wherein 5% (v/v) of bacterial inoculum was employed. The O2 flow rate was maintained at 1.0 L min-1 and the pH at 7.0. Copper nanoparticles (CuNPs), with an average hydrodynamic diameter of 21 ± 1 nm, were synthesized using 25 g.L-1 of mining tailing and a stirring rate of 250 rpm. Aiming to visualize some possible biomedical applications of the as-synthesized CuNPs, their antibacterial activity was evaluated against Escherichia coli and their cytotoxicity was evaluated against Murine Embryonic Fibroblast (MEF) cells. The 7-day extract of CuNPs at 0.1 mg mL-1 resulted in 75% of MEF cell viability. In the direct method, the suspension of CuNPs at 0.1 mg mL-1 resulted in 70% of MEF cell viability. Moreover, the CuNPs at 0.1 mg mL-1 inhibited 60% of E. coli growth. Furthermore, the NPs were evaluated regarding their photocatalytic activity by monitoring the oxidation of methylene blue (MB) dye. The CuNPs synthesized showed rapid oxidation of MB dye, with the degradation of approximately 65% of dye content in 4 h. These results show that the biosynthesis of CuNPs by R. erythropolis using pre-processed mine tailing can be a suitable method to obtain CuNPs from environmental and economical perspectives, resulting in NPs useful for biomedical and photocatalytic applications.

Assessment of the use of red mud as a catalyst for photodegradation of bisphenol A in wastewater treatment.

This study aimed to investigate the use of red mud (RM) - a byproduct of aluminum production, as a photocatalyst, which was characterized physical-chemically and used in the photodegradation of the target compound bisphenol A (BPA). Chemical processing was performed in the RM (acid treatment, chemical reduction and calcination) to verify the most active catalyst. From the results obtained, a complete degradation kinetics of BPA was carried out using a synthetic matrix (BPA in deionized water) and a real matrix (BPA in wastewater) using natural RM/calcined and TiO2 for comparison. The results indicated the potential use of the RM/calcined, which was able to degrade between 88 and 100% of the pollutant in a synthetic sample. Tests on a real effluent sample resulted in degradation rates that ranged from 59 to 100% with chemical oxygen demand reductions of up to 23% using natural RM/calcined in comparison to TiO2. The blank system (irradiation of the solution without the use of a photocatalyst) and the natural RM/calcined one, resulted in reductions of the toxicity in the effluent sample (measured by EC20 using the marine bacteria Vibrio fischeri) of about 12 times, whereas the same treatment using TiO2 resulted in a toxicity reduction of only seven times. Within these results, the RM/calcined showed potential to be used in wastewater treatment in polishing processes.

A friendly environmental material: iron oxide dispersed over activated carbon from coffee husk for organic pollutants removal.

A friendly environmental material for organic contaminants removal was prepared in this work: small particles of iron oxide dispersed over activated carbon from coffee waste for Fenton-like application. The materials were characterized by means of XRD, N2 physisorption, Mössbauer spectroscopy and H2 pulse titration. The composites showed very good catalytic performances for methylene blue organic dye oxidation. The small goethite particles are the predominant iron oxide phase in the composites. The apparent surface area is quite high and is not very affected after iron impregnation. ESI-MS studies revealed that the dye removal occurs through a Fenton-type system by the composite whereas for the activated carbon the dye removal occurs mainly via adsorption. The iron leaching from the catalysts was negligible, less than 0.5 ppm, which evidences the occurrence of a heterogenous oxidation process. The catalyst was very active for methylene blue oxidation and could be repeatedly used for at least 5 cycles. The catalyst was also active in the oxidation of other organic compounds, such as caffeine and atrazine.

Activated carbon prepared from coffee pulp: potential adsorbent of organic contaminants in aqueous solution.

The processing of coffee beans generates large amounts of solid and liquid residues. The solid residues (pulp, husk and parchment) represent a serious environmental problem and do not have an adequate disposal mechanism. In this work, activated carbons (ACs) for adsorption of organic compounds were prepared from coffee pulp by controlled temperature at different pulp/Na2HPO4 ratios (4:1, 2:1, 5:4 and 1:1). The N2 adsorption/desorption isotherms showed ACs with high quantities of mesopores and micropores and specific surface areas of 140, 150, 450 and 440 m(2)g(-1) for AC 4:1, AC 2:1, AC 5:4 and AC 1:1, respectively. The prepared material AC 5:4 showed a higher removal capacity of the organic contaminants methylene blue (MB), direct red (DR) and phenol than did a Merck AC. The maximum capacities for this AC are approximately 150, 120 and 120 mg g(-1) for MB, DR and phenol, respectively. Thus, a good adsorbent was obtained from coffee pulp, an abundant Brazilian residue.

Guest diffusion in interpenetrating networks of micro- and mesopores.

Pulsed field gradient NMR is applied for monitoring the diffusion properties of guest molecules in hierarchical pore systems after pressure variation in the external atmosphere. Following previous studies with purely mesoporous solids, also in the material containing both micro- and mesopores (activated carbon MA2), the diffusivity of the guest molecules (cyclohexane) is found to be most decisively determined by the sample "history": at a given external pressure, diffusivities are always found to be larger if they are measured after pressure decrease (i.e., on the "desorption" branch) rather than after pressure increase (adsorption branch). Simple model consideration reproduces the order of magnitude of the measured diffusivities as well as the tendencies in their relation to each other and their concentration dependence.

Ammonia removal using activated carbons: effect of the surface chemistry in dry and moist conditions.

The effect of surface chemistry (nature and amount of oxygen groups) in the removal of ammonia was studied using a modified resin-based activated carbon. NH(3) breakthrough column experiments show that the modification of the original activated carbon with nitric acid, that is, the incorporation of oxygen surface groups, highly improves the adsorption behavior at room temperature. Apparently, there is a linear relationship between the total adsorption capacity and the amount of the more acidic and less stable oxygen surface groups. Similar experiments using moist air clearly show that the effect of humidity highly depends on the surface chemistry of the carbon used. Moisture highly improves the adsorption behavior for samples with a low concentration of oxygen functionalities, probably due to the preferential adsorption of ammonia via dissolution into water. On the contrary, moisture exhibits a small effect on samples with a rich surface chemistry due to the preferential adsorption pathway via Brønsted and Lewis acid centers from the carbon surface. FTIR analyses of the exhausted oxidized samples confirm both the formation of NH(4)(+) species interacting with the Brønsted acid sites, together with the presence of NH(3) species coordinated, through the lone pair electron, to Lewis acid sites on the graphene layers.

Activated carbon production from industrial yeast residue to boost up circular bioeconomy.

This work aims to obtain activated carbon (AC) from yeast residue to boost up bioeconomy. In this way, carbon was prepared from yeast biomass produced by the ethanol industry and after beta-glucan extraction. Carbon was activated with CO2, water vapor, and a combination of both using an experimental design. The best conditions to produce AC were activation with CO2 for 30 min at 850 °C and CO2 flow of 0.09 L/min, set by experimental design and desirability function to optimize the yield, surface area, and microporosity. Thus, for physical activation with water vapor employing the optimized conditions, it was possible to achieve a yield of 56.6% (m/m) for AC with 1144 m2/g of surface area and mean micropore volume of 0.53 cm3/g. The maximum AC surface area reached 1616 ± 567 m2/g with a yield of 21 ± 1%. The prepared ACs were characterized by elemental analysis, X-ray diffractometry, infrared spectroscopy, thermogravimetry analysis, pHPZC, and potentiometric titration to determine the main functional groups of sorption sites. The carbon obtained from the desirability condition was used to remove dipyrone from synthetic aqueous effluent with an experimental sorption capacity of 88 ± 4 mg/g, being the phenomenon described by the Freundlich isotherm model.

Removal of As(V) and Cr(VI) from aqueous solutions using solid waste from leather industry.

This study evaluated the feasibility of using a solid waste from the leather industry as an adsorbent for removal of Cr(VI) and As(V) from aqueous media. The adsorbent material was characterized by chemical analyses, infrared spectroscopy, and scanning electronic microscopy (SEM) prior to reaction in order to assess its surface properties. Langmuir and Freundlich equations were used for analyzing the experimental data, which showed a better fit to the Langmuir model, thus suggesting a monolayer adsorption process in the surface of the adsorbent. The high amounts of Cr(VI)-133 mg g(-1) and As(V)-26 mg g(-1) adsorbed demonstrates the great potential for using this solid waste from the leather industry as a low-cost alternative to the traditionally used adsorbent materials.

Solid waste from leather industry as adsorbent of organic dyes in aqueous-medium.

The industrial tanning of leather usually produces considerable amounts of chromium-containing solid waste and liquid effluents and raises many concerns on its environmental effect as well as on escalating landfill costs. Actually, these shortcomings are becoming increasingly a limiting factor to this industrial activity that claims for alternative methods of residue disposals. In this work, it is proposed a novel alternative destination of the solid waste, based on the removal of organic contaminants from the out coming aqueous-residue. The adsorption isotherm pattern for the wet blue leather from the Aurea tanning industry in Erechim-RS (Brazil) showed that these materials present high activity on adsorbing the reactive red textile dye as well as other compounds. The adsorbent materials were characterized by IR spectroscopy and SEM and tested for the dye adsorption (reactive textile and methylene blue dyes). The concentrations of dyes were measured by UV-vis spectrophotometry and the chromium extraction from leather waste was realized by basic hydrolysis and determined by atomic absorption. As a low cost abundant adsorbent material with high adsorption ability on removing dye methylene blue (80mgg(-1)) and textile dye reactive red (163mgg(-1)), the leather waste is revealed to be a interesting alternative relatively to more costly adsorbent materials.

Removal of organic dyes using Cr-containing activated carbon prepared from leather waste.

In this work, hydrogen peroxide decomposition and oxidation of organics in aqueous medium were studied in the presence of activated carbon prepared from wet blue leather waste. The wet blue leather waste, after controlled pyrolysis under CO(2) flow, was transformed into chromium-containing activated carbons. The carbon with Cr showed high microporous surface area (up to 889 m(2)g(-1)). Moreover, the obtained carbon was impregnated with nanoparticles of chromium oxide from the wet blue leather. The chromium oxide was nanodispersed on the activated carbon, and the particle size increased with the activation time. It is proposed that these chromium species on the carbon can activate H(2)O(2) to generate HO radicals, which can lead to two competitive reactions, i.e. the hydrogen peroxide decomposition or the oxidation of organics in water. In fact, in this work we observed that activated carbon obtained from leather waste presented high removal of methylene blue dye combining the adsorption and oxidation processes.

The use of piassava fibers (Attalea funifera) in the preparation of activated carbon.

The piassava fiber, residue of the broom industry, was used as precursor for the preparation of activated carbons (AC). AC were prepared by chemical activation with zinc chloride (AC ZnCl(2)) or phosphoric acid (AC H(3)PO(4)) and by physical activation with carbon dioxide (AC CO(2)) or water vapor (AC H(2)O). These materials were characterized by adsorption/desorption of N(2) to determine the BET areas, elemental analysis (CHN), thermogravimetric analysis (TG, DTA) and scanning electron microscopy (SEM). The carbons were tested with respect to their adsorption capacity of methylene blue, reactive red, phenol and metallic ions (Cr(+6), Cu(+2) and Zn(+2)). AC ZnCl(2) presented the highest surface area (1190 m(2)g(-1)) and AC H(3)PO(4), the largest pore volume (0.543 cm(3)g(-1)). AC ZnCl(2) was more efficient in the adsorption of methylene blue, Cr(+6) and Cu(+2) ions. AC H(2)O was the better adsorbent for phenol, while AC CO(2) was better for Zn(+2) ions.

Activated carbon/iron oxide composites for the removal of atrazine from aqueous medium.

The adsorption features of activated carbon and the oxidation properties of iron oxides were combined in a composite to produce new materials for atrazine removal from aqueous medium. Activated carbon/iron oxide composites were prepared at 1/1 and 5/1 mass ratios and characterized with powder X-ray diffractometry (XRD), infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and nitrogen adsorption measurements. The adsorption and oxidation processes were evaluated in batch experiments, in order to monitor the atrazine removal capacity of these composites. The main iron oxide actually present in the composites was goethite (alpha-FeOOH). Impregnation with iron oxide reduced the surface area by its deposition in the activated carbon pores. However, a higher iron concentration promoted a higher oxidation rate, indicating that the efficiency of the oxidation reaction is related with the iron content and not with the pre-concentration of the contaminant on the carbon surface through adsorption process.

Produção de carvão a partir de resíduo de erva-mate para a remoção de contaminantes orgânicos de meio aquoso / Production of charcoal from maté waste to remove organic contaminants from aqueous solution

Neste trabalho, apresenta-se um novo material adsorvente, obtido a partir da pirólise de resíduos da erva-mate. O carvão resultante demonstrou elevada área superficial específica quando comparado com outros materiais pirolisados e elevada capacidade de remoção de contaminantes orgânicos de soluções aquosas. Os valores de área específica apresentados pelos materiais foram de 344, 191 e ~0,5 m² g-1, para o carvão Mate 1, Mate 2 e Mate 3, respectivamente. As isotermas de adsorção mostraram que os carvões apresentam potencial para utilização como adsorvente para compostos orgânicos, tais como: o corante têxtil vermelho reativo, o corante azul de metileno e para o herbicida atrazina, sendo que os máximos de adsorção utilizando o carvão Mate 1 foram de 16, 230 e 30 mg g-1, respectivamente.

In this work we present a new adsorbent material, obtained by maté waste pyrolisis. The resulting charcoal presented high specific area when compared with other pyrolized materials and also high capacity to remove organic contaminants from aqueous solution. The charcoal showed specific area of 344, 191 and ~0.3 m² g-1 for sample Mate 1, Mate 2 and Mate 3, respectively. According to the corresponding adsorption isotherm these materials present good adsorption capacity for reactive textile and methylene blue dyes and the herbicide atrazine. Adsorption maxima were respectively 16, 230 and 35 mg g-1 for such substances, when sample Mate 1 was used.