Green fuel production: processes applied to microalgae

The continuous increase in world energy demand will lead to an energy crisis due to the limited availability of fossil fuels. Furthermore, the use of this energetic resource is responsible for the accumulation of greenhouse gases in atmosphere that is associated with several negative effects on environment. Therefore, it is worth to search for different energy supplies that are renewable and environmentally friendly—carbon neutral fuel. Microalgae are photosynthetic microorganisms that can achieve high oil contents. This oil is suitable for producing biodiesel; thus, microalgae are considered a promising sustainable energetic resource that can reduce the dependence on fossil fuel. Biodiesel production from microalgae includes several steps, such as cell cultivation and harvesting, oil extraction and biodiesel synthesis. Although several attempts have been made to improve biodiesel yields from microalgae, further studies are required to improve biodiesel production rates and to reduce the associated costs. This review shows the recent developments on biodiesel production from microalgae, emphasizing two process concepts: (1) indirect route, in which, after a facultative cell wall disruption method, microalgal oil is recovered in an appropriate solvent and then converted into biodiesel through transesterification and (2) direct route, in which biodiesel is produced directly from the harvested biomass. High biodiesel yields are obtained when both routes are preceded by a cell wall disruption method. In the indirect route, it is possible to apply three different types of solvents to recover microalgal oil. Although there are several concerns about the application of organic solvents, the most promising and cost-effective alternative for lipid recovery is n-hexane. Comparing direct and indirect routes, this study demonstrates that although further studies are required to optimize biodiesel production from microalgae, the available information proposes that the direct route is the most efficient.     

UASB performance for bleached and unbleached kraft pulp synthetic wastewater treatment

This paper presents the performance of two bench scale Upflow Anaerobic Sludge Blanket reactors (UASB) used for the treatment of synthetic substrates that simulate bleached and unbleached cellulose pulp plant wastewaters. The control reactor was fed with diluted black liquor and the treatment reactor with the same substrate plus a mixture of chlorinated organics. The total concentration of the chlorinated compounds was gradually increased from 2.5 mg l-1 to 15.0 mg l-1. The average COD removal efficiency during the last phase of the experiment was 81% in the control reactor and 76% in the treatment reactor. These results indicate the capability of UASB reactors to treat this kind of wastewater and the low impact of the chlorinated organics on COD removal efficiency. The minimum overall chlorinated organics removal efficiency was 71% and the maximum was 99.7%. The experiment indicates that under the conditions used in this research the presence of chlorinated organics does not negatively impact the treatment process.     

Investigation and proposal for reuse of effluents from beneficiated bentonite products

This work is intended to show the characterization of three effluents (X, Y, and Z) derived from laboratory analyses conducted in the quality control department of a beneficiated bentonite products factory in order to present alternatives for their treatment and final disposal according to Brazil's National Solid Waste Policy (Política Nacional de Resíduos Sólidos – PNRS, Law 12,305/2010, Brazil). Analyses to identify the characteristics of the effluents revealed that the pH, salinity, electroconductivity, and total dissolved solids were in agreement with the organic and mineral nature of the effluent constituents: solvent, clay minerals, water, and activating agent. To assess reuse proposals, the effluents were subjected to the following tests: (a) swelling characteristic with effluent X, (b) petrochemical characterization of Y, and (c) swelling characteristic using commercial solvent and activated clay produced with effluent Z. Preliminary results indicate that each of these effluents can be reused variously in the laboratory, as a fuel, or in the original analysis/process.     

The effectiveness of climate action and land recovery across ecosystems,climatic zones and scales

Regional Environmental Change - Avalanche risk changes through time due to climate, landscape and socio-environmental transformations. These drivers exhibit space-time variations as function of...     

Preliminary toxicological assessment of phthalate esters from drinking water consumed in Portugal

This paper reports, for the first time, the concentrations of selected phthalates in drinking water consumed in Portugal. The use of bottled water in Portugal has increased in recent years. The main material for bottles is polyethylene terephthalate (PET). Its plasticizer components can contaminate water by leaching, and several scientific studies have evidenced potential health risks of phthalates to humans of all ages. With water being one of the most essential elements to human health and because it is consumed by ingestion, the evaluation of drinking water quality, with respect to phthalate contents, is important. This study tested seven commercial brands of bottled water consumed in Portugal, six PET and one glass (the most consumed) bottled water. Furthermore, tap water from Lisbon and three small neighbor cities was analyzed. Phthalates (di-n-butyl phthalate ester (DnBP), bis(2-ethylhexyl) phthalate ester (DEHP), and di-i-butyl phthalate ester (DIBP)) in water samples were quantified (PET and glass) by means of direct immersion solid-phase microextraction and ionic liquid gas chromatography associated with flame ionization detection or mass spectrometry due to their high boiling points and water solubility. The method utilized in this study showed a linear range for target phthalates between 0.02 and 6.5 μg L^?1, good precision and low limits of detection that were between 0.01 and 0.06 μg L^?1, and quantitation between 0.04 and 0.19 μg L^?1. Only three phthalates were detected in Portuguese drinking waters: dibutyl (DnBP), diisobutyl (DIBP), and di(ethylhexyl) phthalate (DEHP). Concentrations ranged between 0.06 and 6.5 μg L^?1 for DnBP, between 0.02 and 0.16 μg L^?1 for DEHP, and between 0.1 and 1.89 μg L^?1 for DIBP. The concentration of DEHP was found to be up to five times higher in PET than in glass bottled water. Surprisingly, all the three phthalates were detected in glass bottled water with the amount of DnBP being higher (6.5 μg L^?1) than in PET bottled water. These concentrations do not represent direct risk to human health. Regarding potable tap water, only DIBP and DEHP were detected. Two of the cities showed concentration of all three phthalates in their water below the limits of detection of the method. All the samples showed phthalate concentrations below 6 μg L^?1, the maximum admissible concentration in water established by the US Environmental Protection Agency. The concentrations measured in Portuguese bottled waters do not represent any risk for adult's health.     

Identification of redundant air quality measurements through the use of principal component analysis

This study aims to show how principal component analysis (PCA) can be used to identify redundant measurements in air quality monitoring networks. The minimum number of air quality monitoring sites in Oporto Metropolitan Area (Oporto-MA) was evaluated using PCA and then compared to the one settled by the legislation. Nine sites, monitoring NO₂, O₃ and PM₁₀, were selected and the air pollutant concentrations were analysed from January 2003 to December 2005. PCA was applied to the data corresponding to the first two years that were divided into annual quarters to verify the persistence of the PCA results. The number of principal components (PCs) was selected by applying two criteria: Kaiser (PCs with eigenvalues greater than 1) and ODV₉₀ (PCs representing at least 90% of the original data variance). Each pollutant was analysed separately. The two criteria led to different results. Using Kaiser criterion for the eight analysed periods, two PCs were selected in: (i) five periods for O₃ and PM₁₀; and (ii) six periods for NO₂. These PCs had important contributions of the same groups of monitoring sites. The percentage of the original data variance contained in the selected PCs using this criterion was always below 90%. Thus, the results obtained using ODV₉₀ were considered with more confidence. Using this criterion, only five monitoring sites for NO₂, three for O₃ and seven for PM₁₀ were needed to characterize the region. The number of monitoring sites for NO₂ and O₃ was in agreement with what was established by the legislation. However, for PM₁₀, Oporto-MA needed two more monitoring sites. To validate PCA results, statistical models were determined to estimate air pollutant concentrations at removed monitoring sites using the concentrations measured at the remaining monitoring sites. These models were applied to a year's data. The good performance obtained by the models showed that the monitoring sites selected by the procedure presented in this study were enough to infer the air pollutant concentrations in the region defined by the initial monitoring sites. Additionally, the air pollutant analysers corresponding to the redundant measurements can be installed in non-monitored regions, allowing the enlargement of the air quality monitoring network.     

Prenatal foetal diagnosis of partial trisomy 3q and monosomy 13p due to a maternal balanced rearrangement

The authors describe a case of a male foetus whose ultrasound at 20 weeks' gestation revealed cystic hygroma, cleft lip and ventricular septal defect. Amniotic fluid cytogenetics using GTG banding showed a 46,XY,der(13)t(3;13)(q12;p11.1) rearrangement, and fluorescence in situ hybridization (FISH) delineated the relevant breakpoints. Familial studies identified a maternal balanced translocation involving chromosomes 3 and 13. The post-mortem examination confirmed the prenatal ultrasound findings. Copyright © 2005 John Wiley & Sons, Ltd.     

Development of metal organic framework-199 immobilized zeolite foam for adsorption of common indoor VOCs

Reticulated foam shaped adsorbents are more efficient for the removal of volatile organic compounds (VOCs), particularly from low VOC-concentration indoor air streams. In this study composite structure of zeolite and metal organic frameworks (MOFs), referred as ZMF, has been fabricated by immobilization of fine MOF-199 powder on foam shaped Zeolite Socony Mobil-5 (ZSM-5) Zeolitic structure, referred as ZF. The ZMF possess a uniform and well-dispersed coating of MOF-199 on the porous framework of ZF. It shows higher surface area, pore volume, and VOCs adsorption capacity, as compared to ZF-structure. Post-fabrication changes in selective adsorption properties of ZMF were studied with three common indoor VOCs (benzene, n-hexane, and cyclohexane), using gravimetric adsorption technique. The adsorption capacity of ZMF with different VOCs follow the order of benzene > n-hexane > cyclohexane. In comparison with MOF-199 and ZF, the composite structure ZMF shows improvement in selectivity for benzene from other two VOCs. Further, improvement in efficiency and stability of prepared ZMF was found to be associated with its high MOF loading capacity and unique morphological and structural properties. The developed composite structure with improved VOCs removal and recyclability could be a promising material for small to limited scale air pollution treatment units.