Biofiltration of fugitive methane emissions from landfills using scum from municipal wastewater treatment plants as alternative substrate

Journal of Material Cycles and Waste Management - Biofilters have been recognized as a key technology in the mitigation of greenhouse gases (GHG) emitted by landfills. This study aimed to evaluate...     

Acute toxicity of disinfection by-products from chlorination of algal organic matter to the cladocerans Ceriodaphnia silvestrii and Daphnia similis: influence of bromide and quenching agent

Environmental Science and Pollution Research - Algal organic matter (AOM) in water reservoirs is a worldwide concern for drinking water treatment; once it is one of the main precursors for...     

Influence of palladium content dispersed in the TiO2 photocatalyst for degradation of volatile organic compounds in gas emission

Heterogeneous photocatalysis is highlighted to treat volatile organic compound (VOC) emission. Then, this work analysed the influence of palladium (Pd) content loaded in TiO₂ on n-octane and iso-octane photodegradation. For this, TiO₂ was loaded with Pd in different contents: 0.4%, 0.7%, and 1.0%. The samples were characterized, and the photodegradation experiments were conducted by Pd/TiO₂/UV process. The characterization analyses showed that the metal presence did not change the catalyst structure or its surface area; however, it reduced the bandgap energy. The photocatalytic results proved that palladium improved n-octane degradation from 62% (pure TiO₂) to 92.6% (0.4%Pd/TiO₂) and, iso-octane degradation enhanced from 59% (pure TiO₂) to 90.6% (0.7%Pd/TiO₂); all results were obtained in the space time of 39 s. Therefore, 0.4%Pd/TiO₂ and 0.7%Pd/TiO₂ showed better oxidation results to degradation n-octane and iso-octane, respectively. The kinetic model of pseudo-first order showed a good fit for the data of both VOCs. Heterogeneous photocatalysis with Pd/TiO₂ showed to be an adequate technique to reduce VOCs emission.

     

Woody residues of the grape production chain as an alternative precursor of high porous activated carbon with remarkable performance for naproxen uptake from water

Environmental Science and Pollution Research - Activated carbon prepared from grape branches was used as a remarkable adsorbent to uptake naproxen and treat a synthetic mixture from aqueous...     

Evaluation of boron removal from water by hydrotalcite-like compounds

Layered double hydroxides (LDHs) or hydrotalcite (HT)-like compounds with different kinds of metal ions (Mg-Al and Mg-Fe) in the brucite-like sheets were prepared and their adsorption properties were studied in the boron removal from aqueous solution under laboratory conditions. The hydrotalcites were synthesized by the coprecipitation method and were characterized by chemical analyses, X-ray diffraction (XRD), Fourier Transform infrared spectroscopy (FTIR) and specific surface area measurements (BET). The affinity of these materials with a mixture of B(OH)(3) and B(OH)(4)(-) was studied as a function of contact time, initial pH of the solutions, HT quantity and B concentration (adsorption isotherms). It was found that 120 min is enough time for the equilibrium state to be reached in boron adsorption. Boron removal was independent of the initial pH of the solutions because of the high buffering capacity of the LDHs. On the other hand, the adsorption capacity increases with increasing the adsorbent quantity. The adsorption isotherms, described by the Langmuir model, are of L-type, suggesting that B(OH)(4)(-) is adsorbed preferentially on HT-like materials. Besides, Mg-Al hydrotalcites showed higher adsorption capacity than Mg-Fe. We proposed that in Mg-Al hydrotalcites, the boron removal occurs by both adsorption on external surface and ion exchange, whereas for Mg-Fe it occurs only by surface adsorption. After treatment of a solution containing 5.2 mgBl(-1) with Mg-Al hydrotalcites the final boron concentration reached the recommended limit by WHO for drinking water (0.5 mgl(-1)).     

Dissipation of DDT in a heavily contaminated soil in Mato Grosso, Brazil

After the prohibition of organochlorine-pesticide use in Brazil for controlling insect vector diseases, Mato Grosso State gathered the exceeding DDT and stored it irregularly in an open air area that belongs to the National Health Foundation, causing soil contamination. This study aimed to evaluate the contamination level and dissipation of p,p'-DDT and p,p'-DDE in this area. For that, surface soil samples were collected on 19 September 2000, 15 December 2000, 4 April 2001 and soil samples 30-40 cm; 60-70 cm and 90-100 cm deep were taken from five points in the studied area on 17 July 2001. The contaminants were determined by a small scale method which consists on extraction and clean-up steps combined into one step by transferring soil samples mixed with neutral alumina to a chromatographic column prepacked with neutral alumina and elution with hexane:dichloromethane (7:3 v:v). The eluate was concentrated and the analytes were quantified by gas chromatography with an electron-capture detector. p,p'-DDT at surface soil ranged from 3,800 to 7,300 mg kg(-1). 30-40 cm deep soil sample concentrations varied from 0.036 to 440 mg kg(-1) while 90-100 cm deep samples varied from 0.069 to 180 mg kg(-1). Volatilization is probably the main dissipation process. The p,p'-DDT is moving slowly downward in the soil profile, however, the levels of this contaminant are high enough to present risk to underground waters.     

Strategies for reducing airborne pesticides under tropical conditions

Brazil is currently one of the largest pesticide consumers worldwide. However, a lack of scientific information regarding airborne pollution is still an issue, with tragic consequences to human health and the environment. To reduce pollution of the lower air layers, where pesticide spraying occurs, green barriers that filter the air could be an effective mitigation procedure. Modifying pulverization habits, by pulverizing in the late afternoon instead of in the morning could also reduce pesticide volatilization, while other recommendations with the purpose of lowering the pesticide amounts currently applied are likewise pursued. Data obtained about volatilization have demonstrated that, in order to reduce air pollution risks, one of the most effective preventive strategies is to ban products with high vapor pressure. Global/local stakeholders need to assume the responsibility to find the best way to reduce airborne pesticide pollution, which has increasingly shown disastrous effects as major poisons to human health and the environment.     

The effects of land use change on mercury distribution in soils of Alta Floresta, Southern Amazon

This study presents the spatial distribution, degree of contamination and storage capacity of Hg in surface forest and pasture soils from Alta Floresta, Southern Amazon, a significant gold mining site from 1980 to 1996. During that period, average annual gold production was about 6.5 tons, with an estimated Hg annual emission to the environment of about 8.8 tons, 60-80% of it being emitted to the atmosphere. Mercury sources to the region are mining sites and gold-dealer shops at the city of Alta Floresta, where gold is smelted and commercialized. Mercury concentrations in forest soils (15-248 ng g(-1), average=61.9 ng g(-1)) were 1.5-3.0 times higher than in pasture soils (10-74 ng g(-1), average=33.8 ng g(-1)), suggesting strong re-mobilization after deforestation. Highest Hg concentrations were found within a distance of 20-30 km from mining sites in both soil types. The influence of the refining operations within the city of Alta Floresta, however, was less clear. Somewhat higher concentrations were observed only within a 5 km radius from the city center where gold-dealer shops are located. Wind direction controls the spatial distribution of Hg. Background concentrations (15-50 ng g(-1)) were generally found at the outer perimeter of the sampling grid, about 40 km from sources. This suggests that Hg released from mining and refining activities undergoes rapid deposition. Estimated cumulative Hg burdens for the first 10 cm of soil averaged 8.3 mg m(-2) and 4.9 mg m(-2), for forest and pasture soils respectively and compare well with ultisols and hydromorphic oxisols, but were lower than those found in yellow-red and yellow latosols and podsols from other Amazonian areas. Our results show that changing land use in the Amazon is a strong re-mobilizing agent of Hg deposited on soils from the atmosphere.     

Absorption and translocation of 2,4-D in plants of Memora peregrina

The objective of this work was to evaluate absorption and translocation of the herbicide 2,4-D in plants of Memora peregrina. The herbicide 2,4-D was used alone with the formulation DMA 806 BR and associated with the herbicide picloram in the commercial product Padron. Levels of radioactivity on the treated leaves were determined in sample obtained after washing them with methanol and chloroform at different times after the application of the radiolabelled formulation (1, 2, 4, 8, 24, and 48 h). Translocation was evaluated by cutting plants between stem and root. The parts obtained were: root, stem, leaf treated, leaves above the leaf treated, leaves below the leaf treated, and leaf opposite of the leaf treated. These parts were weighted, dried, ground, burnt, and radioactivity in the samples was determined. The results suggest that the translocation of the radioactive herbicide 2,4-D was insignificant in plants of M. peregrina in the two treatments evaluated. Absorption of 14C 2,4-D in the treatment with DMA 806 BR and the mixture of DMA 806 BR plus Padron had the same behavior. These observations explain the inefficient control obtained with this herbicide in plant species under study.     

Composition analysis of dental solid waste in Brazil

When developing proper waste management strategies, it is essential to characterize the volume and composition of solid waste. The aim of this work was to evaluate the composition of dental waste produced by three dental health services in Belo Horizonte, Minas Gerais State, Brazil. Two universities, one public and one private, and one public dental health service were selected. Waste collection took place from March to November 2007. During this period, three samples were collected from each dental health service. The total amount of dental waste produced in one day of dental work was manually separated into three categories: infectious and potentially infectious waste, accounting for 24.3% of the total waste; non-infectious waste, accounting for 48.1%; and domestic-type waste, accounting for 27.6% (percentages are for mean weights of solid waste). Our results showed that most of the waste considered as biomedical may be misclassified, consequently making the infectious waste amount appear much larger. In addition, our results suggest that the best waste minimization method is recycling, and they help to define an appropriate waste management system in all three of the dental health services involved in this study.