The efficiency of the multi-walled carbon nanotubes used for antibiotics removal from wastewaters generated by animal farms

Environmental Science and Pollution Research - In the recent years, residual antibiotics are considered to be emerging environmental pollutants due to their continuous input and persistence into...     

Effect of ceramic industrial particulate emission control on key components of ambient PM10

The relationship between specific particulate emission control and ambient levels of some PM₁₀ components (Zn, As, Pb, Cs, Tl) was evaluated. To this end, the industrial area of Castellón (Eastern Spain) was selected, where around 40% of the EU glazed ceramic tiles and a high proportion of EU ceramic frits are produced. The PM₁₀ emissions from the ceramic processes were calculated over the period 2000–2006, taking into account the degree of implementation of corrective measures throughout the study period. Abatement systems were implemented in the majority of the fusion kilns for frit manufacture in the area as a result of the application of the Directive 1996/61/EC, leading to a marked decrease in PM₁₀ emissions. By contrast, emissions from tile manufacture remained relatively constant because of the few changes in the implementation of corrective measures. On the other hand, ambient PM₁₀ levels and composition measurements were carried out from 2002 to 2006. A high correlation between PM₁₀ emissions from frit manufacture and ambient levels of Zn, As, Pb and Cs (R² from 0.61 to 0.98) was observed. On the basis of these results, the potential impact of the implementation of corrective measures to reduce emissions from tile manufacture was quantified, resulting in a possible decrease of 3–5 μg/m³ and 2 μg/m³ in ambient mineral PM₁₀ (on an annual basis) in urban and suburban areas, respectively. This relatively simple methodology allows us to estimate the direct effect of a reduction in primary particulate emissions on ambient levels of key particulate components, and to make a preliminary quantification of the possibilities of air quality improvement by means of further emission reduction. Therefore, it is a useful tool for developing future air quality plans in the study area and in other industrialised areas.     

Bioaccumulation of POPs in human breast milk from south of the Russian Far East and exposure risk to breastfed infants

Environmental Science and Pollution Research - The present study is a stage of the regular POP monitoring conducted in the framework of the Russian Federation’s National Implementation Plan...     

Toxicity of two types of silver nanoparticles to aquatic crustaceans Daphnia magna and Thamnocephalus platyurus

Although silver nanoparticles (NPs) are increasingly used in various consumer products and produced in industrial scale, information on harmful effects of nanosilver to environmentally relevant organisms is still scarce. This paper studies the adverse effects of silver NPs to two aquatic crustaceans, Daphnia magna and Thamnocephalus platyurus. For that, silver NPs were synthesized where Ag is covalently attached to poly(vinylpyrrolidone) (PVP). In parallel, the toxicity of collargol (protein-coated nanosilver) and AgNO₃ was analyzed. Both types of silver NPs were highly toxic to both crustaceans: the EC50 values in artificial freshwater were 15–17 ppb for D. magna and 20–27 ppb for T. platyurus. The natural water (five different waters with dissolved organic carbon from 5 to 35 mg C/L were studied) mitigated the toxic effect of studied silver compounds up to 8-fold compared with artificial freshwater. The toxicity of silver NPs in all test media was up to 10-fold lower than that of soluble silver salt, AgNO₃. The pattern of the toxic response of both crustacean species to the silver compounds was almost similar in artificial freshwater and in natural waters. The chronic 21-day toxicity of silver NPs to D. magna in natural water was at the part-per-billion level, and adult mortality was more sensitive toxicity test endpoint than the reproduction (the number of offspring per adult).     

Anaerobic and aerobic transformations affecting stability of dewatered sludge during long-term storage in a lagoon

The goal of this work was to study long-term behavior of anaerobically digested and dewatered sludge (biosolids) in a lagoon under anaerobic and aerobic conditions to determine the stability of the final product as an indicator of its odor potential. Field lagoons were sampled to estimate spatial and temporal variations in the physical-chemical properties and biological stability characteristics such as volatile solids content, accumulated oxygen uptake, and soluble protein content and odorous compound assessment. The analyses of collected data suggest that the surface layer of the lagoon (depth of above 0.15 m) undergoes long-term aerobic oxidation resulting in a higher degree of stabilization in the final product. The subsurface layers (depth 0.15 m below the surface and deeper) are subjected to an anaerobic environment where the conditions favor the initial rapid organic matter degradation within approximately the first year, followed by slow degradation.     

Role and impact of CO2–rock interactions during CO2 storage in sedimentary rocks

Before implementing CO₂ storage on a large scale its viability regarding injectivity, containment and long-term safety for both humans and environment is crucial. Assessing CO₂–rock interactions is an important part of that as these potentially affect physical properties through highly coupled processes. Increased understanding of the physical impact of injected CO₂ during recent years including buoyancy driven two-phase flow and convective mixing elucidated potential CO₂ pathways and indicated where and when CO₂–rock interactions are potentially occurring. Several areas of interactions can be defined: (1) interactions during the injection phase and in the near well environment, (2) long-term reservoir and cap rock interactions, (3) CO₂–rock interactions along leakage pathways (well, cap rock and fault), (4) CO₂–rock interactions causing potable aquifer contamination as a consequence of leakage, (5) water–rock interactions caused by aquifer contamination through the CO₂ induced displacement of brines and finally engineered CO₂–rock interactions (6). The driving processes of CO₂–rock interactions are discussed as well as their potential impact in terms of changing physical parameters. This includes dissolution of CO₂ in brines, acid induced reactions, reactions due to brine concentration, clay desiccation, pure CO₂–rock interactions and reactions induced by other gases than CO₂. Based on each interaction environment the main aspects that are possibly affecting the safety and/or feasibility of the CO₂ storage scheme are reviewed and identified. Then the methodologies for assessing CO₂–rock interactions are discussed. High priority research topics include the impact of other gaseous compounds in the CO₂ stream on rock and cement materials, the reactivity of dry CO₂ in the absence of water, how CO₂ induced precipitation reactions affect the pore space evolution and thus the physical properties and the need for the development of coupled flow, geochemical and geomechanical models.     

Modelling the long-term performance of zero-valent iron using a spatio-temporal approach for iron aging

Zero-valent iron (ZVI) permeable reactive barriers (PRBs) have become popular for the degradation of chlorinated ethenes (CEs) in groundwater. However, a knowledge gap exists pertaining to the longevity of ZVI. The present investigation addresses this situation by suggesting a numerical simulation model that is intended to be used in conjunction with field or column tests in order to describe long-term ZVI performance at individual sites. As ZVI aging processes are not yet completely understood and are still subject to research, we propose a phenomenological modelling technique instead of a common process-based approach. We describe ZVI aging by parameters that characterise the extent and rate of ZVI reactivity change depending on the propagation of the precipitation front through ZVI. We approximate degradation of CEs by pseudo-first order kinetics accounting for the formation of partially dechlorinated products, and describe ZVI reactivity change by scaling the degradation rate constants. Three independent modelling studies were carried out to test the suitability of the conceptual and numerical model to describe the observations of accelerated column tests. All three tests indicated that ZVI reactivity declined with an increasing number of exchanged pore volumes. Measured and modelled concentrations showed good agreement, thereby proving that resolving spatial as well as temporal changes in ZVI reactivity is reasonable.