998 resultados para Metais : Remoção


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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

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Heavy metals are present in industrial waste. These metals can generate a large environmental impact contaminating water, soil and plants. The chemical action of heavy metals has attracted environmental interest. In this context, this study aimed to test t he performance of electrochemical technologies for removing and quantifying heavy metals. First ly , the electroanalytical technique of stripping voltammetry with glassy carbon electrode (GC) was standardized in order to use this method for the quantificatio n of metals during their removal by electrocoagulation process (EC). A nalytical curves were evaluated to obtain reliability of the determin ation and quantification of Cd 2+ and Pb 2+ separately or in a mixture. Meanwhile , EC process was developed using an el ectrochemical cell in a continuous flow (EFC) for removing Pb 2+ and Cd 2+ . The se experiments were performed using Al parallel plates with 10 cm of diameter (  63.5 cm 2 ) . The optimization of conditions for removing Pb 2+ and Cd 2+ , dissolved in 2 L of solution at 151 L h - 1 , were studied by applying different values of current for 30 min. Cd 2+ and Pb 2+ concentrations were monitored during electrolysis using stripping voltammetry. The results showed that the removal of Pb 2 + was effective when the EC pro cess is used, obtaining removals of 98% in 30 min. This behavior is dependent on the applied current, which implies an increase in power consumption. From the results also verified that the stripping voltammetry technique is quite reliable deter mining Pb 2+ concentration , when compared with the measurements obtained by atomic absorption method (AA). In view of this, t he second objective of this study was to evaluate the removal of Cd 2+ and Pb 2+ (mixture solution) by EC . Removal efficiency increasing current was confirmed when 93% and 100% of Cd 2+ and Pb 2+ was removed after 30 min . The increase in the current promotes the oxidation of sacrificial electrodes, and consequently increased amount of coagulant, which influences the removal of heavy metals in solution. Adsortive voltammetry is a fast, reliable, economical and simple way to determine Cd 2+ and Pb 2+ during their removal. I t is more economical than those normally used, which require the use of toxic and expensive reagents. Our results demonstrated the potential use of electroanalytical techniques to monitor the course of environmental interventions. Thus, the application of the two techniques associated can be a reliable way to monitor environmental impacts due to the pollution of aquatic ecosystems by heavy metals.

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Industrial activities like mining, electroplating and the oil extraction process, are increasing the levels of heavy metals such as Cu, Fe, Mg and Cd in aquatic ecosystems. This increase is related to the discharge of effluents containing trace of this elements above the maximum allowed by law. Methods such as ion exchange, membrane filtration and chemical precipitation have been studied as a means of treatment of these metals contamination. The precipitation of metals using anionic surfactants derived from carboxylic acids emerged as an alternative for the removal of metals from industrial effluents. The reaction between bivalent ions and these types of surfactants in aqueous solution leads to the formation of metal carboxylates, which can precipitate in the form of flakes and are subsequently removed by a process of decantation or simple filtration. In this work the metals extraction is performed by using the surfactant sodium hexadecanoate as extracting agent. The main purpose was to study the effect of temperature, solution pH, and concentration of surfactant in the metal removal process. The statistical design of the process showed that the process is directly dependent to changes in pH and concentration of surfactant, but inversely proportional and somewhat dependent to temperature variation, with the latter effect being considered negligible in most cases. The individual study of the effect of temperature showed a strong dependence of the process with the Kraft point, both for the surfactant used as extracting agent, as for the surfactant obtained after the reaction of this surfactant with the metal. From data of temperatures and concentrations of the surfactant was possible to calculate the equilibrium constant for the reaction between sodium hexadecanoate and copper ions. Later, thermodynamic parameters were determined, showing that the process is exothermic and spontaneous.

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Heavy metals are used in many industrial processestheirs discard can harm fel effects to the environment, becoming a serious problem. Many methods used for wastewater treatment have been reported in the literature, but many of them have high cost and low efficiency. The adsorption process has been used as effective for the metal remoal ions. This paper presents studies to evaluate the adsorption capacity of vermiculite as adsorbent for the heavy metals removal in a synthetic solution. The mineral vermiculite was characterized by differents techniques: specific surface area analysis by BET method, X-ray diffraction, raiosX fluorescence, spectroscopy in the infraredd region of, laser particle size analysis and specific gravity. The physical characteristics of the material presented was appropriate for the study of adsorption. The adsorption experiments weredriveal finite bath metod in synthetic solutions of copper, nickel, cadmium, lead and zinc. The results showed that the vermiculite has a high potential for adsorption, removing about 100% of ions and with removal capacity values about 85 ppm of metal in solution, 8.09 mg / g for cadmium, 8.39 mg/g for copper, 8.40 mg/g for lead, 8.26 mg/g for zinc and 8.38 mg/g of nickel. The experimental data fit in the Langmuir and Freundlich models. The kinetic datas showed a good correlation with the pseudo-second order model. It was conducteas a competition study among the metals using vermiculiti a adsorbent. Results showed that the presence of various metals in solution does not influence their removal at low concentrations, removing approximat wasely 100 % of all metals present in solutions

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The acceleration of industrial growth in recent decades on all continents aroused the interest of the companies to counter the impacts produced on the environment, spurred primarily by major disasters in the petroleum industry. In this context, the water produced is responsible for the largest volume of effluent from the production and extraction of oil and natural gas. This effluent has in its composition some critical components such as inorganic salts, heavy metals (Fe, Cu, Zn, Pb, Cd, ), presence of oil and chemicals added in the various production processes. In response to impact, have been triggered by research alternative adsorbent materials for water treatment and water produced, in order to removing oils and acids and heavy metals. Many surveys of diatomaceous earth (diatomite) in Brazil involve studies on the physico-chemical, mineral deposits, extraction, processing and applications. The official estimated Jazi are around 2.5 million tonnes, the main located in the states of Bahia (44%) and Rio Grande do Norte (37,4%). Moreover, these two states appear as large offshore producers, earning a prominent role in research of adsorbents such as diatomite for treatment of water produced. Its main applications are as an agent of filtration, adsorption of oils and greases, industrial load and thermal insulator. The objective of this work was the processing and characterization of diatomite diatomaceous earth obtained from the municipality of Macaíba-RN (known locally as tabatinga) as a low cost regenerative adsorbent for removal of heavy metals in the application of water produced treatment. In this work we adopted a methodology for batch processing, practiced by small businesses located in producing regions of Brazil. The characterization was made by X-ray diffraction (XRD), scanning electron microscopy (SEM) and specific surface area (BET). Research conducted showed that the improvement process used was effective for small volume production of diatomite concentrated. The diatomite obtained was treated by calcination at temperature of 900 oC for 2 hours, with and without fluxing Na2CO3 (4%), according to optimal results in the literature. Column adsorption experiments were conducted to percolation of the in nature, calcined and calcined fluxing diatomites. Effluent was used as a saline solution containing ions of Cu, Zn, Na, Ca and Mg simulating the composition of produced waters in the state of Rio Grande do Norte, Brazil. The breakthrough curves for simultaneous removal of copper ions and zinc as a result, 84.3% for calcined diatomite and diatomite with 97.3 % for fluxing. The calcined fluxing diatomite was more efficient permeability through the bed and removal of copper and zinc ions. The fresh diatomite had trouble with the permeability through the bed under the conditions tested, compared with the other obtained diatomite. The results are presented as promising for application in the petroleum industry

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Comunicação seleccionada e artigo em Livro de Actas

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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

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Dissertação apresentada na Faculdade de Ciências e Tecnologia da Universidade Nova de Lisboa para obtenção de grau de Mestre em Bioenergia

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Dissertação apresentada na Faculdade de Ciências e Tecnologia da Universidade Nova de Lisboa para obtenção do grau de Mestre em Engenharia Sanitária

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Dissertação para obtenção do Grau de Mestre em Engenharia do Ambiente, perfil Engenharia Sanitária

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A fitoextração tem sido sugerida como alternativa viável às práticas tradicionais de recuperação de solos contaminados por metais pesados (remoção do solo e destinação em aterros ou coprocessamento em cimento, etc.), em razão dos menores custos e por ser menos impactante ao ambiente. Este trabalho objetivou avaliar a fitoextração induzida (uso de ácido cítrico como agente quelante) de metais pesados, com o cultivo de aveia-preta (Avena strigosa Schreber), girassol (Helianthus annuus L.) e grama-batatais (Paspalum notatum Flügge), em solos poluídos (solos 2, 3 e 4) de uma área de mineração de Pb em Adrianópolis (PR). O solo 1 foi amostrado em área de mata nativa (referência). O experimento foi realizado em casa de vegetação, com três repetições. Foram determinados os teores de Pb, Cd, Cu, Ni, Cr e Zn no solo com HNO3/HCl (3:1) concentrados. Após a colheita das plantas, determinaram-se a massa de matéria seca e os teores de metais pesados nas raízes e parte aérea (digestão nítrico-perclórica). Os solos contaminados (2, 3 e 4) apresentaram as seguintes faixas de teores de metais pesados (mg kg-1): Pb - 2.598,5 a 9.678,2; Cd - 1,9 a 22,2; Cu - 165,5 a 969,2; Ni - 22,6 a 38,4; Cr - 15,2 a 27,8; e Zn - 87,4 a 894,8. A adição de quelante não induziu a uma absorção mais efetiva de metais pesados pelas plantas. O solo 2 possibilitou melhor crescimento das plantas, e o girassol deve ser preferido na fitorremediação das áreas sob as mesmas condições. Na área próxima à planta fabril (solo 3) e nas áreas com grande ocorrência de rejeitos (solo 4), a fitoextração não foi eficiente. Nesses ambientes, recomenda-se o estudo de outras plantas nativas e, ou, exóticas resistentes a altos teores de Pb (solo 3) ou a remobilização de solo mais rejeito para aterros industriais (solo 4).

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Neste trabalho, avaliou-se o desempenho de dois reatores anaeróbios operados em batelada sequencial (ASBR), instalados em série, em escala-piloto (volumes de 280 L e 140 L, respectivamente), no tratamento de águas residuárias de suinocultura, com concentrações de sólidos suspensos totais (SST) em torno de 10.000 mg L-1. Para o pós-tratamento do efluente do sistema de tratamento com os ASBR, utilizou-se de duas lagoas de polimento (volume de 1.000 L, cada) em série. As cargas orgânicas volumétricas (COV) aplicadas no primeiro ASBR variaram de 4,43 a 12,75 g DQOtotal (L d)-1. As eficiências médias de remoção de nitrogênio total Kjeldahl (NTK) e fósforo total (P-total) variaram de 30 a 82% e de 42 a 100%, respectivamente, no sistema de tratamento anaeróbio composto pelos ASBR seguidos das lagoas de polimento. A utilização das lagoas de polimento em série permitiu manter eficiências médias de remoção acima de 80% para o Fe, Mn e Zn e de 76% para o Cu. O número de coliformes termotolerantes foi reduzido a 8x10³ NMP/100 mL.

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Este estudo foi realizado com o objetivo de se estimar o conteúdo de elementos metálicos presentes em três macrófitas aquáticas submersas, procurando avaliar a participação destas plantas na remoção destes elementos na água e criar base de dados que permita prever o impacto ambiental do descarte delas em solo ou na própria água. As amostras foram desidratadas, moídas e encaminhadas aos laboratórios para análise e quantificação dos elementos. Para as três espécies, a maior concentração de elementos foi observada durante o verão, ocorrendo declínio nas concentrações durante o inverno, principalmente para os elementos vanádio e chumbo. Não foi detectada presença do elemento mercúrio em nenhuma das amostras.

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The produced water is a byproduct formed due to production of petroleum and carries with it a high amount of contaminants such as oil particles in suspension, organic compounds and metals. Thus, these latter pollutants are very difficult to treat because of its high solubility in water. The objective of this work is to use and evaluate a microemulsioned system to remove metals ( K , Mg , Ba , Ca , Cr , Mn , Li , Fe ) of synthetic produced water. For the extraction of metals, it was used a pseudoternary diagram containing the following phases: synthetic produced water as the aqueous phase (AP), hexane as organic phase (OP), and a cosurfactant/surfactant ratio equal to four (C/S = 4) as the third phase, where the OCS (saponified coconut oil) was used as surfactant and n-butanol as cosurfactant. The synthetic produced water was prepared in a bench scale and the region of interest in the diagram for the removal of metals was determined by experimental design called. Ten points located in the phase Winsor II were selected in an area with a large amount of water and small amounts of reagents. The samples were analyzed in atomic absorption spectrometer, and the results were evaluated through a statistical assesment, allowing the efficiency analysis of the effects and their interactions. The results showed percentages of extraction above 90% for the metals manganese, iron, chromium, calcium, barium and magnesium, and around 45% for metals lithium and potassium. The optimal point for the simultaneous removal of metals was calculated using statistical artifact multiple response function (MR). This calculation showed that the point of greatest extraction of metals occurs was the J point, with the composition [72% AP, 9% OP, 19% C/S], obtaining a global extraction percentage about 80%. Considering the aspects analyzed, the microemulsioned system has shown itself to be an effective alternative in the extraction of metals on synthetic produced water remediation