1000 resultados para óxido de zinco


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In this work were prepared composites of iron oxide and carbonaceous materials in two different weight proportions (Carbon/Fe 1/1 and 1/2). The physico-chemical properties of the composites were determined by temperature programmed reduction (TPR), adsorption/dessorption of N2, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and pulse titration H2. The XRD and XPS analysis showed a cubic iron oxide phase, identified as maghemite, formed over the carbon surface. The particle size of maghemite showed to be within 10-30 nm. Carbon/Fe 1/2 was the most active in MB removal kinetics and ESI-MS studies showed that MB removal by both composites leads to oxidized intermediates.

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Nitrous oxide emissions from an activated sludge plant which serves a research institute in Rio de Janeiro city were estimated from six unit processes (grit tank, sand trap, aeration tank, secondary settling tank, sludge recirculation line and aerobic digester sludge tank) and also from the plant effluent. Total estimated annual flux was 3.2 x 10(4) g N2O yr-1 of which about 90% was from the aeration tank. Emission factors estimated from population served, wastewater flow and nitrogen load (conversion ratio) were 13 g N2O person-1 yr-1, 9.0 x 10-5 g N2O Lwastewater-1 and 0.14%.

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Iron oxide nanoparticles were synthesized in microemulsion systems composed by Triton X-100/hexyl alcohol/cyclohexane/aqueous solution. The nanoparticles were synthesized in microemulsions containing different amounts of ammonium, in order to evaluate the influence of this parameter on the size of the nanoparticles and on the phase transformation after heat treatment. Powder materials were obtained after centrifugation, washing and drying, and they were analyzed as synthesized and after heating at 350, 500 and 1000 °C. It was observed that the higher amount of ammonium induced smaller particles and minor phase transformation, possibly due to a preferential nucleation process.

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Surface sediments from the River São Francisco were analyzed to investigate the impact, due to the presence of metals (Cd, Cu, Pb, Zn) in wastes from a metallurgical industry in the city of Três Marias/MG, Brazil. The concentrations and geochemical associations of Pb, Zn and trace metals associated with the minerals employed in zinc production were measured. Sediments close to discharge locations were highly contaminated with Pb (332-512 μg g-1) and Zn (7872-10780 μg g-1), with values decreasing rapidly due to dilution and hydraulic sorting. Evaluation of toxicity according to the Consensus-based Sediment Quality Guidelines indicated for Cd, Pb and Zn a high probability of adverse effects on aquatic biota at these sites.

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This paper describes the adsorption of heavy metals ions from aqueous solution by hydrous niobium oxide. Three heavy metals were selected for this study: cadmium, lead and silver. Adsorption isotherms were well fitted by Langmuir model. Maximum adsorption capacity (Q0) for Pb2 +, Ag+ and Cd2 + was found to be 452.5, 188.68 and 8.85 mg g-1, respectively.

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In this work, hydrotalcite, a layered double hydroxide, had its adsorption and ion exchange properties combined with the magnetic properties of iron oxide to produce a magnetic adsorbent, HT-Fe. The removal of As(V) by a HT-Fe adsorbent was evaluated under various conditions. The Kinetic process was well described by a pseudo-second order rate model. The maximum adsorption capacity, calculated with the Langmuir model showed to be dependent on pH, reaching values of 24.09, 10.19 and 7.44 mg g-1, respectively, for pH values of 4.0, 7.0 and 9.0. The inhibition by competition of anions is dependent on the type of ionic species.

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Materials containing aluminum and iron oxide were synthesized through the preparation of hybrid spheres and tested in the dehydrogenation of ethylbenzene in the presence of CO2. The catalytic results suggest that the high initial ethylbenzene conversion is due to the contribution of basic sites. These results also point to a competitive process between CO2 adsorption and the oxidative dehydrogenation of ethylbenzene for the basic sites (lattice oxygen). In spite of the coke deposition is originating from ethylbenzene and CO2, the amount of carbonaceous deposits was smaller with the presence of CO2, if compared with the dehydrogenation in the absence of CO2.

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Mn, Zn, Fe, Cd, Pb and Hg were determined in Zn-C and alkaline batteries manufactured along almost 20 years. After samples disassembly the electroactive components were treated with aqua regia in bath ice for 24 h. Metals were analyzed by ICP-OES. Zn and Mn amounts did not vary significantly. Fe amount decreased, specially after 2000. Hg, Cd and Pb amounts dramatically decreased along time, being virtually absent in alkaline batteries manufactured after 2005. Pb still remains in Zn-C samples. Scanning electron microscopy of batteries manufactured in 1997 and 1998 showed the presence of Bi, In and Cr in the plastic/paper anode-cathode separator.

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Lead metallurgy at Adrianópolis is the largest environmental problem of Paraná, Brazil. The objective of this study was to determine Pb and Zn levels in water and sediment in two catchments by different extraction methods. The high levels of lead in water in most of samples do not allow the human use. Total Pb concentration as high as 795.3 µg L-1 was observed in Ribeira River bank, in a pluvial water stream flowering from a abandoned factory. Due to the high Pb levels in sediments from some sites (maximum of 24,300 mg kg-1) is recommended to avoid the water turbulence.

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Spent alkaline and Zn-C batteries were placed in seawater, rainwater or landfill leachate at room temperature for up 30 days in order to simulate natural weathering. After the experiments pH and electrical conductivity of the liquid were measured. The precipitate formed and the filtrate were submitted to metal analysis by ICP-OES. Seawater is the most corrosive medium, followed by landfill leachate. Pb, Cd and Hg were mainly in the filtrate. Fe, Mn and Zn were generally dominant in the precipitate. Na and K account for the electrical conductivity and are good indicators of the corrosion stage of the batteries.

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This work describes methodologies for speciation analysis of the metals copper and zinc as total, total dissolved, labile, as well as complexation capacity (conditional stability constants and available ligand concentration), using the same technique, differential pulse anodic stripping voltammetry (DPASV). Several supporting electrolytes were tested, and the results showed that KNO3 and HNO3 resulted in voltamograms without interferences as well as excellent resolution for the total and labile fractions. The methodology using the DPASV technique allows a simple and low cost analysis of copper and zinc speciation, with high precision and sensitivity, with limits of quantification (LOQ) of 1.8 nmol L-1 for copper and 2.1 nmol L-1 for zinc.

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This work aimed to access the contents and chemical forms and to estimate mobility and availability of cooper and zinc in samples from two soils (Haplortox and Paleudult) previously treated with doses of sewage sludge (SS) and municipal solid waste compost (MSWC), besides a control treatment. Largest percentages of Cu and Zn were determined in the organic matter fraction. Zn showed higher percentages of soluble and exchangeable fractions than Cu. Treatments with SS showed higher potential of Cu and Zn availability. Modifications in soil attributes due to residue application affected metal mobility and availability indexes.

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Nine absorbents were prepared using a mixture of Amazonian kaolinite and MnO2 at three temperatures (600, 700 and 900 ºC) in order to retain Pb2+ ions contained in the battery solutions. The batch experiments carried out with the batteries used water for 3 h and the kinetic isotherm was fitted with the pseudo-second order Lagergren equation. Findings show that synthesized adsorbents AD4, AD5 and AD7 performed well in reducing the Pb2+ ion content from 0.36 to 0.00 mg g-1. The better performance for removing the Pb2+ ions occurred for adsorbents synthesized in the temperature range from 600 to 700 ºC.

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Zn availability in Red Latossol (Rhodic Ferralsol) of different pH amended with different rates of sewage sludge was studied by the isotopic 65Zn L value method. Soil chemical properties were found to be altered by SS addition. Zn concentration and Zn derived from SS (ZnpfSS) in plant, and Zn phytoavailability (L value), were increased with increasing SS rates. The linear correlation coefficient of plant Zn with SS rates and with L value was significant at 1% probability. The L value proved an efficient method for predicting Zn phytoavailability in sewage sludge-amended soil with different pH under the soil conditions studied.

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Soil fluxes of N2O were determined over one year in montane tropical rainforest of southeastern Brazil with average annual rainfall of 2.8 m. Annual mean (± standard deviation) and median N2O fluxes were 3.0 ± 1.4 and 2.7 µg N m-2 h-1, respectively, is 5-10 times lower than mean values reported in literature for tropical rainforest soils in the Amazon basin. N2O fluxes varied spatially and seasonally, were about twice as high during summer as in winter, and significantly influenced by both monthly precipitation and soil temperature.