To investigate the reaction of calcium hydroxide with CO2 and SO2 simultaneously, a gas containing both gases reacted with the calcium base at 58 ºC and a relative humidity of 55 %. Different CO2 and SO2 concentrations were performed being the composition of the gas stream 12, 6 or 0 % CO2; 5000, 2500, 1000 or 0 ppm SO2, 9.5 % synthetic air and balanced N2, with a flue gas rate of 1000 mL/minute. A continuous gas analyzer controlled the CO2 and SO2 concentrations in the effluent gas and the breakthrough curves of both gases were obtained. The gas analyzer data show that SO2 and CO2 compete to react with the base reacting simultaneously. By using thermogravimetry (TG), differential scanning calorimetry (DSC) and mass spectrometry (MS) techniques, calcium sulphite hemihydrate, CaSO3.1/2H2O, was identified as the unique desulfurization product detected. CaSO4 was not identified although O2 was present in the gas mixture. CaCO3 was the main product of the reaction of calcium hydroxide and CO2 being the complex CaO.CO2 another possible product synthesized in low amounts. From analyzer data it was proved that a part of the CaCO3 present in the sorbent or synthesized in the process reacts with the SO2 and release CO2. Results of this work show that the combination of continuous gas analyzer data and TG-DSC-MS techniques, not used before to study this reaction, is a good and easy way to clarify the process and the products of reaction. | Our acknowledgment to M.C. y T. for financial support of this work under Project MAT 2010-18862.

Cantabria is a small region located in Northern Spain that combines different land uses; thus, urban, industrial and rural areas are present in a relatively small area (5300 km2); however, the anthropogenic influence is evident by studying the deposition of metals towards these areas. Three sampling sites (industrial, urban and rural) were selected to assess the variability in metal deposition. Sampling was carried out monthly (from January 2012 to July 2012) using a bulk (funnelbottle) sampler. As, Cd, Cr, Cu, Mn, Mo, Ni, Pb, Ti, Zn and V were determined in the water-soluble and in the insoluble fractions of deposition samples. The impact of the human activities in the industrial area can be seen on several metals such as Pb, Zn, Cu and Mn. The most obvious influence was found for Mn, high fluxes were measured in the industrial site with a mean value of 2260 μg/m2·day; in contrast to urban (99.6 μg/m2·day) and rural (15.3 μg/m2·day) areas. The lowest flux values were found in the rural area for all the elements. Enrichment Factor (EF) analysis were also studied for the three sites. The high EFs values found for Pb, Mn, Cu, and Zn (>100) in the industrial site point to significant anthropogenic sources, mainly originated from industrial activities (steel and ferro-manganese alloy manufacturing plants) and road traffic.

The use of peracetic acid (PAA) in the disinfection of sanitary effluents has been proposed by various authors. However, there are still doubts about its influence on the physical-chemical characteristics of the effluent after application. In the present study, it was observed that the composition of PAA leads to an increase in organic material, resulting in an increase of approximately 20 mg/L in the chemical oxygen demand of the effluent for every 10 mg/L of PAA applied. According to the kinetic tests, the degradation of PAA in the effluent was represented by a first-order reaction and its half-life in the effluent was estimated at 79 min. The formation of by-products resulting from degradation of PAA in the effluent was evaluated by considering by-products already detected by other authors in disinfection trials, these being nonanal, decanal, chlorophenols, and 1-methoxy-4-methylbenzene, which were not observed in the effluent being studied after application of PAA at a dosage of 10 mg/L. © 2013 Springer Science+Business Media Dordrecht.

The volatile monoterpene alpha-pinene has been measured in sediments of a selected area at "Carlos Anwandter" Nature Sanctuary, a Ramsar protected wetland located at the northwest of Valdivia City, south-central Chile. The ecosystem was seriously damaged by an uncontrolled liquid emission of a pulp mill (CELCO-Arauco) located about 15 km upstream of Rio Cruces during 2004. Exploratory data analysis was applied to analytical data collected from sediment samples, having found alpha-pinene as a reiterative chemical at relatively high concentrations in some specific areas of the wetland. The decrease of the total concentration of alpha-pinene in the area under study is coincident with a point contamination that occurred during 2004 (12,240 ng g(-1)) showing a decay in 2005 (7,890 ng g(-1)) and middle of 2006 (4,060 ng g(-1)). The following years, last 2006, 2008, and 2009, show a relatively constant concentration with a clear tendency toward baseline levels (2,460-2,640 ng g(-1)). Since the decrease of concentrations of alpha-pinene in sediments in the period 2004-2009 shows an opposite trend as compared to the surface area increase of pine and eucalyptus plantation in Region de Los Rios, and not having found potential sources of alpha-pinene by anthropogenic activities other than the pulp mill in the area under study, it may be finally concluded that this compound did not enter the bodies of water from a gradual and natural process; instead there is a base to sustain anthropogenic input. alpha-Pinene in sediments may be a plausible chemical tracer capable of detecting pollution events over time and its impacts in aquatic ecosystems as well as changes in aquatic ecosystems produced by improperly treated pulp mill liquid emissions that use pine and eucalyptus species.

The effectiveness of activated carbon sample (Carbonₑₓₚ) prepared by KOH chemical activation in hampering oligomerization of multicomponent adsorption was systematically examined. Anoxic (absence of molecular oxygen) and oxic (presence of molecular oxygen) adsorption isotherms of single-solute (2,4-dimethylphenol), binary solute (2-methylphenol/2,4-dimethylphenol), and ternary solute (phenol/2-methylphenol/2,4-dimethylphenol) were studied, using Carbonₑₓₚ and commercial granular activated carbon F400. Both binary solute adsorption and ternary solute adsorption on Carbonₑₓₚ indicated no impact of the presence of molecular oxygen on the adsorptive capacity. No significant differences between oxic and anoxic environment were noticed for any multicomponent adsorption systems, which indicated the effectiveness of Carbonₑₓₚ in hampering the oligomerization of phenolic compounds. On the other hand, in F400, which has lower microporosity and acidic functional groups, significant increases in the adsorptive capacity had been observed when molecular oxygen was present.

Heavy metals occur naturally in soil, at concentrations that depend on the parent material from which the soil was formed, the processes of formation, and the composition and the proportion of the components of its solid phase. Quantifying these concentrations is important for environmental studies of soil contamination and pollution, and choosing the methods for doing so is a key step in establishing heavy metal contents in soil samples. We evaluated two digestion methods (aqua regia and EPA 3051, both microwave oven-assisted) for assessing pseudo-total concentrations of Cd, Co, Cr, Cu, Ni, Pb and Zn in the surface layer (0–20 cm) of soil samples from the Brazilian agricultural frontier in the southwestern Amazon. Nineteen composite samples of the most representative soil classes for the states of Mato Grosso and Rondônia were collected under native vegetation undisturbed by human intervention. Canonical discriminant analysis and principal component analysis were used for multivariate exploration of the data. Aqua regia extracted higher amounts of Co, Ni, Pb, and Zn than EPA 3051, while levels of Cr and Cu did not differ between methods. In general, aqua regia recovered more of the metals when compared to reference soil samples.

With the constant development of new ionic liquids, the understanding of the chemical fate of these compounds also needs to be updated. To this effect, the interaction of a number of novel ionic liquids with soils was determined. Therefore, three novel headgroups (ammonium, phosphonium, or pyrrolidinium) with single or quaternary substitution were tested on a variety of soils with high-to-low organic matter content and high-to-low cation exchange capacity, thereby trying to capture the full range of possible soil interactions. It was found that the ionic liquids with single butyl alkyl chain interacted more strongly with the soils (especially with a higher cation exchange capacity), at lower concentrations, than the quad-substituted ionic liquids. However, the quad-substituted ionic liquids interacted more strongly at higher concentrations, due to the double-layer formation, and induced stronger dipole interaction with previously sorbed molecules.

Geochemical characterization of two landfills, one closed and the other still active, both located near Komotini (Thrace, Greece), has been carried out. The aim was to provide an integrated and reliable methodology for a rapid assessment of the real impact of a municipal solid waste landfill, in the main environmental matrices (air and water) of the surrounding areas. The chemical (CO₂, CH₄, CO, H₂, N₂, and O₂ + Ar) and isotopic characterization (δ¹³C₍CO₂₎ and δ¹³C₍CH₄₎) of landfill gas and chemical (Na⁺, K⁺, Ca²⁺, Mg²⁺, Cl⁻, SO₄ ²⁻, HCO₃ ⁻, NH₄ ⁺, NO₃ ⁻, NO₂ ⁻, B, COD, Fe, Mn, As, Cr, Ni, Cu, Zn, Cd, Pb, and Hg) and isotopic analysis (δD, δ¹⁸O, tritium content, and δ¹³CDIC) of leachate, stream waters and groundwaters, and flux survey on the air–soil interface has been carried out. Combined chemical and isotopic analysis of the fluids collected inside and in the surroundings of the Komotini landfills supply a detailed picture of biogas emission and composition as well as of leachate chemistry and interaction with local waters. The results arising in this case study demonstrate that it is possible to propose a quick and reliable geochemical protocol to get a detailed picture of the state of health of the environment around a landfill.