In indirect olfactometry analysis, to avoid condensation or adsorption processes during or storage of the sample, containers made of suitable materials should be used. Also, reaction between the chemicals during transport from the source of the odour to the research laboratory is an important process which can influence on examinations’ results. Study included determination of the odour and compound concentrations of six gas mixtures. Gas samples were collected by silicone hoses into Tedlar® bags and tested by Nasal Ranger, SM-100 olfactometers and Photovac Voyager gas chromatograph. Time of keeping gas in bags was 78 h, and concentration of compounds was measured every hour, eight times per day. For benzene, acetone, 1,1-dichloroethylene, c-1,2-dichloroethylene, t-1,2-dichloroethylene, methyl ethyl ketone and vinyl chloride, 100 % decrease of concentration has been noticed within 78 h of holding in the bag. Average rate of loss of most compounds concentration was from 0.01 to 2.50 % for the first 30 h and from 0.35 to 18.50 % during the last 48 h of examination. Decreasing of odour concentration measured by Nasal Ranger (NR) in all series was between 0.00 and 4.98 % till 30 h, between 1.91 and 100 % in the last 48 h of test and between 1.61 and 100 % in 78 h. In case of odour concentration measured by SM, those values were, respectively, 1.26–4.93 %, 1.39–4.93 % and 2.40–3.18 %. Values of average rate of intensity decreasing were, respectively, 0.77–1.75 %, 2.36–4.67 % and 1.18–2.07 %. Statistically significant correlation coefficients for compound concentrations and intensity, odour concentration obtained by SM-100 as well as NR were, respectively, 0.55–0.97, 0.47–0.99 and 0.37–0.98.

Ozone and ozone-based advanced oxidation processes were applied for the treatment of a recalcitrant wastewater generated by wood-based industries that contains different inorganic and organic constituents and high chemical oxygen demand (COD) varying between 3,400 and 4,000 mg/L. The investigation used a tubular ozone reactor combined with an UV reactor designed for different hydraulic retention times. The dependent variables addressed to evaluate the treatment efficiency were the reduction of COD and total organic carbon (TOC) and the biodegradability of the treated effluent based on respirometric studies using activated sludge from a wastewater treatment. The results showed that even though ozonation alone at acid pH promoted COD and TOC reductions of 65 and 31 % respectively, a decrease in the biodegradability was observed. The most effective treatment (COD and TOC reductions of 93 and 43 %, respectively) was obtained when applying ozone combined with UV light at basic pH. The ozone-UV combination was capable of increasing the amount of readily available COD by 75 % with an additional reduction of TOC by 60 %. In conclusion, ozonation at low pH effectively reduces the COD content in wastewater generated by the wood-based industry; however, in order to combine advanced oxidation with biological process, ozone combined with UV is recommended.

The effect of glyphosate on richness and structure of the Rhizobiaceae and total bacterial communities in an agricultural soil after different treatments was studied. The herbicide was applied on the soil in the presence or the absence of Medicago sativa plants with or without inoculation with the Sinorhizobium meliloti reference strain RCR2011. Terminal-restriction fragment length polymorphism (T-RFLP) profiling showed that this agricultural soil has a high total microbial and rhizobial genetic diversity. To investigate the impact of the herbicide on microbial activity, fluorescein diacetate (FDA) and a panel of three enzymes (phosphatase, catalase, and protease BAA) were assessed. Depending on the type of enzyme tested, the enzymatic activities responded differently to the action of glyphosate, the presence of M. sativa, and the inoculation with RCR2011. The present work gives original insights into the effect of the herbicide on the rhizospheric area of M. sativa with or without rhizobial inoculation by the fact that glyphosate changes microbial diversity and affects soil enzymatic activities.

This paper presents the results of a study on mercury distribution in urban wells from the town of Almadén (central Spain), a site that not only hosted the world’s largest mercury mine but also a large roasting plant for cinnabar (HgS). The study includes data on Hg contents in the underground waters and also quality and physical-chemical parameters such as pH, conductivity, oxidation-reduction potential (ORP), dissolved oxygen, and water temperature from 27 wells and 2 monitoring drill holes. An important proportion of the wells (16 %) display Hg concentrations above the European Union Commission (EUC) and Spanish threshold (at 1 μg L⁻¹) and only 10 % exceeded the US EPA recommendation (at 2 μg L⁻¹). As expected, the highest concentrations of dissolved and total Hg are found in wells near to the mine. Hydrochemical water types depend on geogenic and anthropogenic factors, for example, higher mercury concentrations are linked to water-rock interactions (e.g., oxidation, leaching) in sectors where soluble mercury compounds have formed. Hg concentrations show a decrease from 2013 to 2015, a fact that may be due to the encapsulation of the main calcines waste dump or to dilution effects related to strong rainfall events previous to the sampling survey.

In the present work, the role of chemical compounds of one abundant vegetable waste, exhausted coffee, on Cr(VI), Cu(II), and Ni(II) sorption has been investigated. For this purpose, exhausted coffee was subjected to sequential extractions by using dichloromethane (DCM), ethanol (EtOH), water, and NaOH 1 %. The raw and treated biomass resulting from the extractions were used for metal ions sorption. Sorption results were discussed taking into consideration polarity and functional groups of raw and treated biomass. In general, the successive removal of extractives led to an insignificant increase in the studied metal ions sorption after DCM, EtOH, and water. The sorption results using free-extractive materials showed that metal sorption can be effectively achieved without this non-structural fraction of the sorbent. Alkaline hydrolysis destroyed in part the structural compounds of the sorbent resulting in an insignificant decrease of chromium removal while a significant increase of copper and nickel sorption was observed. The determination of elemental ratios of exhausted coffee and all treated biomass evidenced the involvement of oxygen functional groups in copper and nickel sorption. FTIR analysis confirmed the involvement of lignin moieties in the chromium sorption by exhausted coffee. As a final remark, this study shows that the sequential extraction opens new expectations to the total valorisation of lignocellulosic-based biomasses. The extractives can be removed and used as a biosource of valuable compounds, and the resulting waste can be used as a sorbent for metal ions keeping the same capacity for metal sorption as the non-extracted biomass.

Because of the low energy costs in the absence of the need for aeration, the non-requirement of a carbon source and alkali, and the reduced production of excess sludge, anaerobic ammonia oxidation (Anammox) has been extensively studied as an alternative to the conventional nitrification–denitrification pathway for biological nitrogen removal from wastewater. However, many challenges remain which need to be overcome to prepare the process for engineering application. These include the long doubling time of Anammox bacteria/autotrophic ammonia-oxidizing bacteria (AAOB), the low tolerance capacity to substrate concentration, and high sensitivity to various environmental factors. This review article focuses on the main drawbacks of the Anammox process and evaluates the progress made to date with regard to the enrichment of AAOB and the treatment performance of the Anammox process itself. The factors affecting the nitrogen removal performance of the Anammox process, such as substrate concentration, organic matters, and variation of temperature, are also reviewed and discussed. Finally, the need for the development of long-term storage methods for AAOB is addressed.

For many years, atmospheric mercury has been perceived as a global pollutant. Transport of mercury compounds in the atmosphere and its deposition on the earth’s surface is an important issue that requires knowledge regarding the circulation of the various forms of this metal between environmental components. There are many numerical models that can be used to study and image this phenomenon. These models are based on data concerning mercury emission sources, concentrations of this contaminant on modelling areas and meteorological data to assess air mass inflow on a regional and global scale. A method to assess mercury deposition fluxes on a local scale based only on stream intensity analysis of mercury is proposed in this study. Mercury deposition fluxes (bulk) that were assessed by the MDC method at the Zloty Potok station (regional background station for the Silesian Agglomeration) varied from 22.8 μg · m⁻² · year⁻¹ (an 8-month period in 2013) to 54.2 μg · m⁻² · year⁻¹ in 2012. Developing procedures to estimate the mercury deposition coefficient (MDC) is useful in areas where only meteorological parameters and mercury concentrations in the atmospheric air are measured. The obtained deposition coefficient values enable quantification of a selected pollutant concentration and its potential impact resulting from deposition.

The present and past mining activity left several abandoned tailings and dams in the Panasqueira tin–tungsten mining area. Seasonal water samples and stream sediments were collected during two different periods (rainy and dry seasons) and analyzed for a wide range of major and trace elements, in order to define the present hydrochemical situation. Rain waters interact with the altered sulfides stored in the tailings which generate runoff waters with high metal concentrations. The waste material derived from the exploitation enhanced acidification and metal-releasing processes, due to the increase in the specific surface, which favors the oxidation of sulfide minerals. Acid drainage and high metal(loid)s (Cd, Fe, Mn, Zn, Cu, As) concentrations in solution were observed in waters leaching the Panasqueira tailing deposits. In dry season, generally the acidic waters, enriched in metals, evaporate progressively depositing sulfate efflorescences characteristic of acidic environments. The elements distribution in precipitated minerals helps in the interpretation of aqueous geochemical data. Aqueous concentrations may be attenuated by goethite, gibbsite, and/or ferrihydrite precipitation in the oxidation zone through adsorption processes. The use of these waters for human consumption and for irrigation represents a threat to humans as they have a potential carcinogenic risk, especially due to the As concentrations. The acid water precipitation is present on the stream sediments, with concentrations exceeding the toxicity limits. Stream sediments are good receptors of metals and metalloids transported by waters. The enrichment factor values, of heavy metal(loid)s from Casinhas stream and Zêzere river sediments, are extremely high in Ag, As, Cd, and Cu revealing enrichments for these potential toxic elements. Igₑₒvalues shows that samples are strongly to very strongly polluted for Ag, As, Bi, Cd, and Cu. According to the consensus-based SQGs, 80 % of the samples were classified at the level of great concern and adverse biological effects are to be expected frequently in this area.

Sixty years of air pollution from two Cu-Ni smelting plants (“Pechenganikel” and “Severonikel”) in the Kola region in northwest Russia have posed a severe threat for water quality, specifically acidification, in subarctic lakes. In the last two decades, emissions of SO2, Cu and Ni from the smelters have declined with 33 %, 40 % and 36 %, respectively. The 75 lakes in Kola Peninsula were sampled with 5-year intervals for the period 1990 to 2010. In addition, were analysed for major anions and cations, DOC and heavy metals. The lakes were grouped according to geology and distance to emission sources into 6 subregions. The most acid-sensitive lakes are located on granites, quartz sands or in highlands. Since 1990, ANС has increased, which is connected to the reduction of the contents strong acids in water (sulphate, chloride) while base cations concentrations have been almost unchanged. Despite the reduction of sulphate, concentrations of alkalinity have not increased in lake water. We have found an increase in concentration of dissolved organic carbon (DOC) and nutrients in Kola lake waters over a 20-year period. We suggest this phenomenon can be explained by two mechanisms: a reduction in deposition of strong acids and warming climate. Concentrations of Ni and Cu have decreased 5-10-fold over the last 20 years. We conclude that reduced emissions from Cu-Ni smelting plants has led to improved water quality in the Kola region.

In the present study, facile and competent homogeneous liquid–liquid microextraction via flotation assistance (HLLME-FA) method combined with flow injection flame atomic absorption spectrometry (FI-FAAS) was proposed for simultaneous separation/preconcentration and determination of trace amounts of cadmium and copper in water samples. The efficient 2-(3,4-dihydroxyphenyl)-1,3-dithiolane (DHPDTO) with thiol groups was used as chelating reagent. The predominant parameters influencing the HLLME-FA, such as solution pH, concentration of DHPDTO, extraction and homogeneous solvent types and volumes, ionic strength, and extraction time were studied. Applying all the optimum conditions in the process, the detection limits of 0.008 and 0.01 μg L⁻¹, linear ranges of 0.08–40 and 0.1–45 μg L⁻¹, and the precision (RSD%, n = 7) of 3.4 and 3.9 % were obtained, respectively, for cadmium and copper. The proposed procedure showed satisfactory results for analysis of tap water, river water, well water, and seawater.