Combined chemical treatment of pharmaceutical effluents from medical ointment production

Three wastewater samples from a pharmaceutical plant formulating medical ointments were subjected to lab-scale treatment by a Fenton-like system in combination with lime coagulation. All samples were plant pre-treated by adsorption/flocculation/filtration processes with utilization of bentonite, but the quality of effluents did not comply with the regulations for wastewater discharged to local sewerage. The optimization of Fenton-like oxidation demonstrated the highest process efficacy at H(2)O(2)/COD weight ratio of 2:1, H(2)O(2)/Fe(2+) molar ratio of 10:1 and 2h of treatment time. The fast pH decrease to acidic values approximately 3 during first min of oxidation for all effluents suggested that pH adjustment was unnecessary. Combination of Fe(III) precipitation and lime coagulation proved feasible to improve considerably COD and residual iron concentration reduction in pharmaceutical effluents. Additionally, considerable BOD(7) reduction and BOD(7)/COD ratio improvement of pharmaceutical wastewater samples was achieved by combined treatment. The application of Fenton-like oxidation with subsequent iron (III)/lime coagulation did not only enhance the quality of pharmaceutical effluents with different chemical characteristics and help to meet the requirements for wastewater discharged to sewage, but also improve the biodegradability of pharmaceutical effluents.     

Assessment of the influence of climatic factors on concentration levels of volatile organic compounds (VOCs) in canadian homes

A nationwide study of indoor air concentrations of 26 VOCs was conducted in Canada in 1991. The study design was based upon random selection of private residences from 1986 Census data and incorporated a temporal stratification feature that allowed sampling of residences in each of four regions of the country at different times of the year with equal probability. Average 24 h concentrations of 26 VOCs in 754 residences were obtained by a passive monitoring method. Initially, climatic parameters were found to have the second highest relative weight among 14 factors identified by factor analysis. Further analysis by linear regression showed that individual VOC concentrations and average outdoor temperature or relative humidity were poorly correlated (r > 0.13). Detailed analysis of the data from four regions of Canada also gave poor correlations between household VOC concentrations and temperature or relative humidity. Concentrations of all 26 VOCs averaged 7.8 μg m⁻³ in winter, 10.3 μg m⁻³ in spring, 4.4 μg m⁻³ in summer and 10.8μ m⁻³ in fall. The highest concentrations of individual compounds averaged 84μm⁻³ for toluene in the spring and 42 μg m⁻³ in the fall, and 44 μg m⁻³ for decane in the spring and 48 μg m⁻³ in the fall. Segregation of the results into outdoor temperature ranges of 0°C, 0–15 and > 15°C gave mean indoor VOC concentrations of 10.3, 9.8 and 50μgm⁻³, respectively. Further examination of the results revealed that the likely presence of sources within homes had a far greater influence on indoor concentrations than ventilation which is partly influenced by climate.     

LivestockPlus: Forages,sustainable intensification,and food security in the tropics

The increased use of grain-based feed for livestock during the last two decades has contributed, along with other factors, to a rise in grain prices that has reduced human food security. This circumstance argues for feeding more forages to livestock, particularly in the tropics where many livestock are reared on small farms. Efforts to accomplish this end, referred to as the ‘LivestockPlus’ approach, intensify in sustainable ways the management of grasses, shrubs, trees, and animals. By decoupling the human food and livestock feed systems, these efforts would increase the resilience of the global food system. Effective LivestockPlus approaches take one of two forms: (1) simple improvements such as new forage varieties and animal management practices that spread from farmer to farmer by word of mouth, or (2) complex sets of new practices that integrate forage production more closely into farms’ other agricultural activities and agro-ecologies.     

Polychlorinated biphenyls-containing electrical insulating oil contaminated soil treatment with calcium and magnesium peroxides

Calcium and magnesium peroxides were applied for the treatment of soil contaminated by polychlorinated biphenyls-containing electrical insulating oil (Aroclor 1016). The removal of PCB-containing electrical insulating oil was achieved with the addition of either calcium peroxide or magnesium peroxide alone and dependent on dosages of the chemical. A 21-d treatment of 60% watered soil with the moderate addition (chemical/oil weight ratio of 0.005/1) of either calcium peroxide or magnesium peroxide resulted in nearly complete (96 ± 2%) oil removal, unsubstantial increase in soil pH and almost no changes in oxygen consumption and dehydrogenase activity, making it suitable for the soil decontamination.     

CO2 mineral sequestration in oil-shale wastes from Estonian power production

In the Republic of Estonia, local low-grade carbonaceous fossil fuel--Estonian oil-shale--is used as a primary energy source. Combustion of oil-shale is characterized by a high specific carbon emission factor (CEF). In Estonia, the power sector is the largest CO(2) emitter and is also a source of huge amounts of waste ash. Oil-shale has been burned by pulverized firing (PF) since 1959 and in circulating fluidized-bed combustors (CFBCs) since 2004-2005. Depending on the combustion technology, the ash contains a total of up to 30% free Ca-Mg oxides. In consequence, some amount of emitted CO(2) is bound by alkaline transportation water and by the ash during hydraulic transportation and open-air deposition. The goal of this study was to investigate the possibility of improving the extent of CO(2) capture using additional chemical and technological means, in particular the treatment of aqueous ash suspensions with model flue gases containing 10-15% CO(2). The results indicated that both types of ash (PF and CFBC) could be used as sorbents for CO(2) mineral sequestration. The amount of CO(2) captured averaged 60-65% of the carbonaceous CO(2) and 10-11% of the total CO(2) emissions.     

Predicting CO2 and SO2 emissions in the Baltic States through reorganization of energy infrastructure

The paper deals with predicting carbon dioxide and sulphur dioxide emissions generated by power production sector in the Baltic States in period up to year 2020. The economies of Lithuania, Latvia and Estonia are rapidly growing therefore forecast of emissions related with this occurrence becomes very important. The Ignalina Nuclear Power Plant (INPP), one of the largest in the world, is situated in the region. Two power production scenarios are modelled to investigate changes in power sector's emissions expected as the consequences of the coming closure of Ignalina NPP. Power market was assumed to be common for all three Baltic countries and was modelled by applying the Balmorel model. The planned closure of Ignalina NPP will bring restructuring of Lithuania power production sector and will change also power transmission between countries. Predictive identified the potential of investments for new modern power generation technologies. At the same time, modelling results show in both scenarios that CO(2) and SO(2) emissions from power production in the Baltic region will increase. The increment of emissions is discussed in the context of meeting requirements of UNFCCC Kyoto protocol and EC Directives. Despite of CO(2) emissions increase the Kyoto protocol's requirements may be expected. At the same time, SO(2) formation in Lithuania power sector may exceed the limits of the EU Council Directive 2001/80/EB therefore the additional measures to control SO(2) emissions have to be investigated.     

Comparing the desorption and biodegradation of low concentrations of phenanthrene sorbed to activated carbon,biochar and compost

Carbonaceous soil amendments are applied to contaminated soils and sediments to strongly sorb hydrophobic organic contaminants (HOCs) and reduce their freely dissolved concentrations. This limits biouptake and toxicity, but also biodegradation. To investigate whether HOCs sorbed to such amendments can be degraded at all, the desorption and biodegradation of low concentrations of ¹⁴C-labelled phenanthrene (?5 μg L^?1) freshly sorbed to suspensions of the pure soil amendments activated carbon (AC), biochar (charcoal) and compost were compared. Firstly, the maximum abiotic desorption of phenanthrene from soil amendment suspensions in water, minimal salts medium (MSM) or tryptic soy broth (TSB) into a dominating silicone sink were measured. Highest fractions remained sorbed to AC (84 ± 2.3%, 87 ± 4.1%, and 53 ± 1.2% for water, MSM and TSB, respectively), followed by charcoal (35 ± 2.2%, 32 ± 1.7%, and 12 ± 0.3%, respectively) and compost (1.3 ± 0.21%, similar for all media). Secondly, the mineralization of phenanthrene sorbed to AC, charcoal and compost by Sphingomonas sp. 10-1 (DSM 12247) was determined. In contrast to the amounts desorbed, phenanthrene mineralization was similar for all the soil amendments at about 56 ± 11% of the initially applied radioactivity. Furthermore, HPLC analyses showed only minor amounts (<5%) of residual phenanthrene remaining in the suspensions, indicating almost complete biodegradation. Fitting the data to a coupled desorption and biodegradation model revealed that desorption did not limit biodegradation for any of the amendments, and that degradation could proceed due to the high numbers of bacteria and/or the production of biosurfactants or biofilms. Therefore, reduced desorption of phenanthrene from AC or charcoal did not inhibit its biodegradation, which implies that under the experimental conditions these amendments can reduce freely dissolved concentration without hindering biodegradation. In contrast, phenanthrene sorbed to compost was fully desorbed and biodegraded.     

Experiences from phasing out the use of mercury in Sweden

The Swedish parliament has decided that the use of mercury (Hg) in society should be phased out by the target year 2000 and substituted with alternative, less harmful elements or compounds. This is to reduce exposure to the toxic heavy metal, levels of which have increased two to seven times in the Swedish environment during the last century. Mercury in products and goods in use in Sweden has been estimated at 100 tonnes Hg, which will slowly be released into the environment if no preventative measures are taken. To avoid handing over unsolved environmental problems and connected costs to future generations, the Swedish government commissioned the Swedish Environmental Protection Agency (EPA) to improve the efficiency of Hg collection and to find a solution for terminal storage of the waste. The result is that the Swedish EPA considers deep storage in rock, accompanied by technical measures to further reduce the risk of future Hg emissions to be the safest method. It has funded approximately 50 projects with the goal of spreading information about the Hg problem and removing Hg from society. The projects have focused on areas where there is a great risk of Hg in products and goods entering the environment. About 6 tonnes Hg has so far been collected in these projects – end of 1999 – and the cost of the Hg collected has varied between 70 and 1300 US$ kg^–1 Hg. The projects were more cost-effective than traditional inspection by an official due to local participation, use of Hg-tracker dogs, and employment of professional electricians in the search for Hg. The involvement of school children and the public has resulted in an increased awareness of environmental matters, and, together with the emptying of water seals, reduced Hg levels in municipal sewage sludge. Electronic Publication