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The need to use renewable sources and matrices with energy potential is widely recognized. The development of innovative technologies aimed at the improvement of energy conversion processes and reducing environmental impacts is currently receiving increasing attention from the scientific community and policymakers. The presence of sugars in airborne particle materials is attributed to biomass combustion. For this reason, these compounds are considered markers of biomass burning. The purpose of this work was to evaluate the emissions produced by agroforestry biomass burning (citrus pruning) by simultaneously sampling both stack emissions and atmospheric particulates in the area around a biomass boiler to understand the real contribution of biomass burning to atmospheric pollution. The combustion tests were carried out by comparing the processes with and without particulate abatement system to see how biomass combustion's contribution to particulate emission can be controlled and reduced. During the tests, the focus was on particulate matter (PM) speciation in terms of sugar marker identification and determination. This study aims to increase knowledge to better understand the contribution of biomass plants to air pollution and differentiate it from the contributions of other sources, such as vehicular traffic or domestic heating. [ABSTRACT FROM AUTHOR]

Rice cultivation stands as the primary agricultural activity in Asia, generating a substantial amount of agricultural waste. Unfortunately, this waste is often disposed of through burning, contributing to severe environmental, health and climate issues. This study presents the characterization of PCDD/Fs, PCBs and PAHs. The emissions were quantified using a fixed-grid-system biomass plant and measuring the macro-pollutants online and sampling the organic micro-pollutants and metals in isokinetic mode, followed by ISO and CEN standards methods. Additionally, the role of agrochemicals was monitored in terms of metal catalysis resulting in POP emissions. This study provides the comprehensive characterization of the most relevant groups of pollutants (metals, PCDD/Fs, PCBs and PAHs) resulting from agricultural waste combustion. Prominent catalytic metals quantified were Cu (22–48 µg/Nm3) and Fe (78–113 µg/Nm3). Rice straw samples from AJK exhibited higher values of organochlorine micro-pollutants compared to those from Punjab and Sindh, i.e., ∑PCDD/F (2594 > 1493 > 856 pg/Nm3) and ∑PCB (41 > 38 > 30 pg/Nm3), respectively, whereas the organic micro-pollutants ∑c-PAH, indicators of incomplete combustion (PICs), were recorded high in the samples from Sindh followed by Punjab and AJK. The average EF is 100 pg/kg, 2.2 pg/kg and 1053.6 µg/kg for ∑PCDD/F, ∑PCB and ∑c-PAH. This study supports the idea that the phenomena leading to the formation of dioxin and dioxin-like compounds are influenced not only by poor combustion but also by the presence of metal catalysts in the burned fuel. [ABSTRACT FROM AUTHOR]

Brake wear emission is a significant contributor to vehicle-related particulate matter, especially in areas with high traffic density and braking frequency. Only recently, non-exhaust emissions from car brake wear have been regulated under Euro 7 regulation, which introduces emission limits for both brake and tires. It also introduces a standard brake particle assessment procedure which includes sampling procedure and measurement techniques defined in the Global Technical Regulation on brakes from light-duty vehicles up to 3.5 t. Over the years, various experimental setups have been tried leading to non-comparable results. The brake wear particle emissions, expressed as emission factors, are mostly estimated as particle mass or particle number and described using different units (e.g., mg/stop brake, mg/km brake; particle number/cm3) making the comparison between studies very difficult. The aim of the present literature review is to present the state-of-the-art of different experimental methods tuned for assessing brake wear emissions, including electric vehicles. The experiments are carried in close, semi-closed, and open systems, and depending on the experimental design, different sampling methods are applied to reduce particle transport loss and guarantee the efficiency of the particle sampling. Driving condition (e.g., speed and applied pressure), formulation of brake materials, and friction temperature have been found to strongly affect the emission characteristics of brake particles, and this needs to be considered when designing study procedures. The findings reported in this review can be beneficial to policy makers and researchers. [ABSTRACT FROM AUTHOR]

Polychlorodibenzo-p-dioxins (PCDDs), polychlorodibenzofurans (PCDFs), and polychlorobiphenyls (PCBs) are semi-volatile compounds and can be partitioned in the atmosphere between the gas and particulate phase, due to their physicochemical properties. For this reason, the reference standard methods for air sampling include a quartz fiber filter (QFF) for the particulate and a polyurethane foam (PUF) cartridge for the vapor phase, and it is the classical and most popular sampling method in the air. Despite the presence of the two adsorbing media, this method cannot be used for the study of the gas-particulate distribution, but only for a total quantification. This study presents the results and the performance aim to validate an activated carbon fiber (ACF) filter for the sampling of PCDD/Fs and dioxin-like PCBs (dl-PCBs) using laboratory and field tests. The specificity, precision, and accuracy of the ACF in relation to the QFF + PUF were evaluated through the isotopic dilution technique, the recovery rates, and the standard deviations. Then the ACF performance was assessed on real samples, in a naturally contaminated area, through parallel sampling with the reference method (QFF + PUF). The QA/QC was defined according to the standard methods ISO 16000–13 and -14 and EPA TO4A and 9A. Data confirmed that ACF meets the requirements for the quantification of native POPs compounds in atmospheric and indoor samples. In addition, ACF provided accuracy and precision comparable to those offered by standard reference methods using QFF + PUF, but with significant savings in terms of time and costs. [ABSTRACT FROM AUTHOR]

Forestry woodchip and spent mushroom compost have commercial potential as sustainable residues in biological and chemical processes for energy production. This study focuses on the evaluation of agri-food industry waste energy valorization, with the aim to reduce the valuable biomass utilization for energy production without decreasing the process quality, thereby pursuing economic and environmental advantages. Burning trials were conducted in a fluidized bed biomass plant provided with emission abatement systems. The biomass mixture used for combustion was composed of pine and oak woodchip and spent mushroom compost. The biomass used was first characterized through compositional and energetic analysis, and subsequently, during the burning tests, a monitoring sampling campaign was carried out to analyze the gas and particles emission. Optimal combustion conditions were observed during combustion, with good oxidation of the organic material, relatively high CO2 production, and low CO concentration in flue gas. Nevertheless, SO2 concentrations in the combustion flue gas are greater than those found in the combustion of the most commonly used biomasses. In fact, the mixture compositional characterization revealed a non-negligible concentration of sulfur, which explains the high values of SO2 detected in emission. The obtained results confirm that controlled combustion, together with suitable biomasses utilization, preliminary characterization, and emission monitoring, are essential practices for the realization of a sustainable process, both from an energy and environmental point of view. [ABSTRACT FROM AUTHOR]

Agricultural activities lead to the production of large quantities of pruning and residual biomass, the correct disposal of which is a topic of great interest. Unfortunately, although it is an environmentally unacceptable practice, disposal often takes place with uncontrolled combustion in field (open burning). Disposal using biomass boilers produces energy from controlled combustion and the use of abatement systems reduces emissions that are inevitably generated in the combustion processes of solid fuel (CO, CO2, NOx, SO2, PM, etc.). Among the pollutants produced in combustion processes, Persistent Organic Pollutants (POPs) are one of the most relevant groups of chemicals that must be monitored for their effect on human health and the environment. This paper reports the data obtained for the emissive characterization of POPs of three different wood biomass prunings (Olive, Citrus and Grapevine) focusing on VOCs, PAHs, PCBs, PCDD/Fs. Emissions samplings were performed at the stack during combustion in a 30 kWth boiler equipped with a multicyclone filter bag for PM abatement in an isokinetic mode in accordance with the CEN and ISO standards methods. Through this work, a complete emission profile of VOCs, PAHs, PCBs, and PCDD/Fs of three different biomass types is provided for the first time, showing that the use of biomass boilers produces quantities of pollutants below the regulatory limits and still lower than those produced by open burning phenomena. Citrus has shown, regarding the other two essences, elevated concentrations in terms of Σ PAH = 174.247 ng/m3, while Olive gave higher results in terms of PCBs and PCDD/Fs (respectively, 39.769 and 3390.63 TEQ pg/Nm3). This is probably due to the high concentration of iron in this biomass (711.44 mg/kg), which during combustion is a catalyst (together with copper) of PCDD/Fs. [ABSTRACT FROM AUTHOR]

Due to the increasing tattoo practicing in Eastern countries and general concern on tattoo ink composition and safety, the green tattoo inks Green Concentrate by Eternal, for European and "for Asia Market Only" were analyzed, under the premise that only the former falls under a composition regulation. A separation of the additives from the pigment was carried out by successive extraction in solvents of different polarities, i.e., water, acetone and dichloromethane. The solid residues were analyzed by IR and Raman spectroscopies, the liquid fractions by GC/mass spectrometry. The relative pigment load and element traces were also estimated. We found that the European and the Asian inks are based on the same pigment, PG7, restricted in Europe, though at different loads. They have a similar content of harmful impurities, such as Ni, As, Cd and Sb and both contain siloxanes, including harmful D4. Furthermore, they have different physical-chemical properties, the European ink being more hydrophilic, the Asian more hydrophobic. Additionally, the Asian ink contains harmful additives for the solubilization of hydrophobic matrices and by-products of the phthalocyanine synthesis. Teratogenic phthalates are present as well as chlorinated teratogenic and carcinogenic compounds usually associated to the laser treatment for removal purposes, to a larger extent in the European ink. The composition of the inks does not seem to reflect regulatory restrictions, where issued. [ABSTRACT FROM AUTHOR]

The tattoos removal has become an issue upon spread of the tattooing practice worldwide and hindsight regrets. Lasers are typically used for the purpose, though some colours such as green are considered "recalcitrant" to the treatment. In the current investigation, we aim at determining the efficacy of removal of a green ink water dispersion, using 5 laser treatments: Nd:YAG nano- and picosecond lasers in normal and array mode and Ruby nanosecond laser, keeping the total irradiated energy constant. The UV–Vis spectroscopy of the treated samples indicate that Nd:YAG picosecond laser is most effective, and the Ruby nanosecond laser is the least efficient. Fragment compounds generated from the pigment and siloxanes are common to all treatments, whereas hydrocarbon emerge by a larger amount upon Nd:YAG nanosecond treatment. Fibres are formed upon picosecond treatments and when operating in array mode, and lamellae are achieved by Ruby nanosecond laser treatment. Residual particles suspensions are very heterogeneous upon nanosecond treatments. [ABSTRACT FROM AUTHOR]

Comparative laser and thermal treatments were carried out on PG36, a green phthalocyanine-based pigment, permitted in European countries where legislation on tattoo composition was issued. Prior to the treatments, PG36 was characterized by SEM imaging, EDX, IR and UV–Vis spectroscopies, revealing an excess of Si and C and O as compared to the pure halogenated Cu-phthalocyanine. Laser treatments were carried out with a Nd:YAG device applied to H2O and propan-2-ol dispersions. Pyrolysis and calcinations were carried out in air or under N2 flow. The outcome of the different procedures was analyzed by UV–Vis spectroscopy, GC–mass spectrometry, X-ray diffraction of the solid residues, SEM microscopy and dynamic light scattering. The comparative analysis indicated the production of different fragment compounds depending on the treatment, (pyrolysis or laser), and, to some extent, to the solvent of the dispersion, with pyrolysis generating a larger number of hazardous compounds. Hydrocarbons and cyclic siloxanes present as additives in PG36 were stable or degraded depending on the treatment. The morphology of the products is also treatment-dependent with nanoparticles < 20 nm and fibers being produced upon laser treatments only. Based on the experimental findings, the equivalence of laser and thermal treatments is evaluated. [ABSTRACT FROM AUTHOR]

Three cases are reviewed of radioactive material with anomalous decay after ultrasound irradiation. In the pure element thorium-228 in distilled water, the radioactivity decreased faster after cavitation than the natural decay. The more complex molecule of Nickel Nitrate, made of radioactive nickel-63, in solution of nitric acid and distilled water was investigated before and after ultrasound irradiation. The X-rays produced by Bremsstrahlung of the electrons from the beta decay of Ni-63 were recorded and a 13% decrease of intensity was measured after 100 s of sonication. A decrease of nickel and an increase of other elements was detected by mass spectrometry in the sonicated sample. The Cobalt-57 decay was investigated by detecting the gamma and X-ray intensity from the Iron-57 resulting after its beta emission. In this third case too, an anomalous decay was observed after sonication. These three cases of anomalous behavior can be explained at the light of the Deformed Space–Time theory. It assumes that a suitable sudden variation of energy density can induce a local deformation of space–time, thus violating the Local Lorentz Invariance. This variation can be created by the ultrasounds in the matter, thus, allowing reactions that cannot occur in a flat (Minkowskian) space–time. The "neutralization" of a radionuclide occurs when it undergoes a DST transformation changing the radionuclide into non-radioactive nuclides. [ABSTRACT FROM AUTHOR]

The radioactivity reduction of a system containing Ni-63 radioactive nuclei after an appropriate ultrasound treatment in an apparatus designed on purpose is reported. The application of ultrasounds for 200 s resulted in the partial disappearance of about 13% of the radioactive Ni-63 nuclei and the appearance of nonradioactive elements. The formation of new elements, not belonging to the decay chain of Nickel-63, is a strong issue where strong nuclear reactions transform Nickel into different elements rather than the usual weak interaction, responsible for the decay, which is accelerated. This way, the time necessary to halve the intensity is shortened by about 20 years, without altering the Ni-63 decay constant, which is 1 4 6. 0 0 ± 2. 1 6  years. Two cases producing similar effects in other radioactive systems after ultrasound treatment are described in the literature and support this finding, which is not forecast by the commonly accepted theories. A theory able to explain these and other results is also reported. [ABSTRACT FROM AUTHOR]

The European and American methods for the determination of polychlorodibenzo- p-dioxins and polychlorodibenzofurans in stationary source emissions require a high-resolution mass spectrometer detector. At the same time, all of the 17 toxic 2,3,7,8-chlorine-substituted isomers have to be separated by an appropriate chromatographic method. The resulting analysis has long runtimes and sometimes a double-column run is needed, which results in a huge waste of time, money and manual labor. To obtain a fast and cost-effective but still reliable analytical system, a single-column gas chromatography with hydrogen as carrier gas and tandem mass spectrometry detection is proposed. The use of hydrogen as the carrier gas is a good choice to shorten runtimes and improve the chromatographic resolution, while tandem mass spectrometry is a well-known alternative for this analysis. All the chromatographic and mass spectrometric parameters fill the requirements of the reference methods with a 35% reduction of runtimes. The accuracy is tested with three fly ash samples of a proficiency interlaboratory test. A good correlation between the results is obtained ( R2 = 0.992, slope = 0.9675), and no coelutions are noted. The system robustness is tested during 5 years of constant use and the maximal relative standard deviation of the relative response factor is 18.8%. [ABSTRACT FROM AUTHOR]

CO2adsorption on synthetic zeolites has become a consolidated approach for biogas upgrading to biomethane. As an alternative to synthetic zeolites, tuff waste from building industry was investigated in this study: indeed, this material is available at a low price and contains a high fraction of natural zeolites. A selective adsorption of CO2and H2S towards CH4was confirmed, allowing to obtain a high-purity biomethane (CO2<2 g m−3, i.e. 0.1%; H2S <1.5 mg m−3), suitable for injection in national grids or as vehicle fuel. The loading capacity was found to be 45 g kg−1and 40 mg kg−1, for CO2and H2S, respectively. Synthetic gas mixtures and real biogas samples were used, and no significant effects due to biogas impurities (e.g. humidity, dust, moisture, etc.) were observed. Thermal and vacuum regenerations were also optimized and confirmed to be possible, without significant variations in efficiency. Hence, natural zeolites from tuffs may successfully be used in a pressure/vacuum swing adsorption process. [ABSTRACT FROM AUTHOR]

Indoor aerosol sources may significantly contribute to the daily dose of particles deposited into the human respiratory system. Therefore, it is important to characterize the aerosols deriving from the operations currently performed in an indoor environment and also to estimate the relevant particle respiratory doses. For this aim, aerosols from indoor combustive and non-combustive sources were characterized in terms of aerosol size distributions, and the relevant deposition doses were estimated as a function of time, particle diameter and deposition site in the respiratory system. Ultrafine particles almost entirely made up the doses estimated. The maximum contribution was due to particles deposited in the alveolar region between the 18th and the 21st airway generation. When cooking operations were performed, respiratory doses per unit time were about ten-fold higher than the relevant indoor background dose. Such doses were even higher than those associated with outdoor traffic aerosol. [ABSTRACT FROM AUTHOR]

Cement plants are responsible for particle and gaseous emissions into the atmosphere. With respect to particle emission, the greater part of is in the range from 0.05 to 5.0 µm in diameter. In the last years attention was paid to submicron particles, but there is a lack of available data on the emission from stationary sources. In this paper, concentration and size distribution of particles emitted from four cement kilns, in relationship to operational conditions (especially the use of alternative fuel to coal) of the clinker process are reported. Experimental campaigns were carried out by measuring particles concentration and size distribution at the stack of four cement plants through condensation particle counter (CPC) and scanning mobility particle sizer spectrometer (SMPS). Average total particle number concentrations were between 2000 and 4000 particles/cm3, about 8–10 times lower that those found in the corresponding surrounding areas. As for size distribution, for all the investigated plants it is stable with a unimodal distribution (120–150 nm), independent from the fuel used. Implications: The study provides information on submicron particles emitted from cement kilns in different driving conditions. In particular, the total particle number is modest and considerably lower than that measured in ambient air, whereas the particle size distribution could be influenced by the operational conditions. [ABSTRACT FROM AUTHOR]

Nitrous oxide (N2O) is the third most important greenhouse gas after carbon dioxide and methane, and contributes about 6% to the greenhouse effect. Nitrous oxide is a minor component of the atmosphere, and it is a thousand times less than carbon dioxide (CO2). Nevertheless, it is much more potent than CO2and methane, owing to its long stay in the atmosphere of approximately 120 yr and the high global warming potential (GWP) of 298 times that of CO2. Although greenhouse gases are natural in the atmosphere, human activities have changed the atmospheric concentrations. Most of the values of emission of nitrous oxide are still obtained by means of emission factors and not actually measured; the lack of real data may result in an underestimation of current emissions. The emission factors used for the calculation of N2O can be obtained from the “Guidelines for the implementation of the national inventory of emissions” of the Intergovernmental Panel on Climate Change, which refer to all nations for the realization of their inventory. This study will present real data, measured in several Italian cement plants with different characteristics. The work also shows a comparison between N2O concentration measured with in situ Fourier transform IR (FTIR) and the reference method EN ISO 21258 based on nondispersive IR (NDIR), in order to investigate the interfering compounds in the measurement with NDIR.Implications:N2O may arise as an unwanted by-product of nitrogen oxide (NOx) abatement systems, in particular selective noncatalytic reduction (SNCR). Since it is applied in the cement plants, N2O emission from cement industry is evaluated, with both FTIR and NDIR instrument. Several considerations emerged from the results. First of all, the emission from this industrial sector is not negligible, and for that reason N2O concentration should be regulated; another observation is that the reference method based on the NDIR technique is not as selective as FTIR could be. [ABSTRACT FROM PUBLISHER]

The combustion of biomass is a process that is increasingly used for the generation of heat and energy through different types of wood and agricultural waste. The emissions generated by the combustion of biomass include different kinds of macro- and micropollutants whose formation and concentration varies according to the physical and chemical characteristics of the biomass, the combustion conditions, the plants, and the operational parameters of the process. The aim of this work is to evaluate the effect of biomass moisture content on the formation of volatile organic compounds (VOCs) during the combustion process. Wet and dry poplar chips, with a moisture content of 43.30% and 15.00%, respectively, were used in a cogeneration plant based on a mobile grate furnace. Stack's emissions were sampled through adsorbent tubes and subsequently analyzed by thermal desorption coupled with the GC/MS. The data obtained showed that, depending on the moisture content of the starting matrix, which inevitably influences the quality of combustion, there is significant variation in the production of VOCs. [ABSTRACT FROM AUTHOR]

A method to measure the emissive concentration of 5-ethylidene-2-norbornene (ENB), a reactive compound used in industrial synthesis of terpolymers, has been developed. The starting points for the development of the presented method are European and Italian reference methods for the quantification of nonreactive volatile organic compounds in industrial emission. In this study, sampling conditions and desorption solvent have been optimized in laboratory and the method was applied in an industrial plant. The laboratory tests showed a good recovery (88-95 %). The concentrations of ENB in industrial emission obtained with the developed method were compared with an online gas chromatography-flame ionization results ( R > 0.97). In addition, several manual measurements were performed in parallel, and the resulting %RSD repeatability was <9 %. The developed method provides a discontinuous technique to measure reactive volatile organic compounds using easy-to-use instruments and assures a very good accuracy and precision even with high-humidity gas flows. The method could be extended to other reactive compounds of the same class. [ABSTRACT FROM AUTHOR]

A comprehensive clean-up method for quantitative analysis of polychlorinated biphenyls (PCBs) and polychlorinated dibenzo-p-dioxins and dibenzo-furans (PCDD/Fs) in one single extract of environmental samples was developed. Since the chemical nature and toxicity of planar PCBs are similar to those of PCDD/Fs, dioxin-like PCBs and PCDD/Fs are often surveyed together in their exposure assessments. The development of a method for the simultaneous analysis of PCBs and PCDD/Fs in environmental samples is invaluable. The automated clean-up system evaluated in this work consists of three additional steps after traditional extraction: the chromatography on gel permeation (GPC), the concentration of the solvent through the use of an in-line evaporation module and the further purification and separation of PCDDs/Fs and dl-PCBs on an alumina cartridge in the ‘SPE module’. In this work, three fly ash samples from an interlaboratory study with different PCDD/F and PCB levels were Soxhlet-extracted and then cleaned up using an automated system. PCDD/Fs and PCBs were determined using isotope dilution and high resolution gas chromatography/high resolution mass spectrometry. The determined values of 17 PCDD/Fs were consistent with the certified values and the relative standard deviations (RSDs) of the determined values were less than 20%. The recoveries of 13C labeled PCDD/Fs and planar PCBs, and their RSDs were within the ranges specified in EPA1613 and 1668a methods, respectively. An accurate and reliable method was successfully developed and can be used in the simultaneous analysis of PCDD/Fs and planar PCBs in environmental samples. [ABSTRACT FROM AUTHOR]

The Stockholm Convention on Persistent Organic Pollutants (POPs) was signed in May 2001 by 127 countries. Currently, 12 substances are regulated by the convention, and the work on finding new candidate chemicals to the convention has started. Among these 12 substances, dibenzo-p-dioxins (PCDDs), polychlorinated dibenzofurans (PCDFs) and polychlorinated biphenyls (PCBs) are the objects of this study. There are no European standard methods for the simultaneous determination of these microorganic compounds, together with polycyclic aromatic hydrocarbons (PAHs) in ambient air—they must be referred to three different methods developed by the U.S. Environmental Protection Agency (EPA). The quali-quantitative analysis of these microorganic pollutants is an important challenge due to the low concentrations at which they may be present. In this study, the development of a simplified, alternative, fast and affordable sampling method for the determination of PAHs, PCDDs, PCDFs and PCBs in ambient air was performed. The sampling time was extended from 24 h to 7 d in order to enrich the sample, to fall within the instrumental limits of detection and to reduce the number of samples to be processed and, therefore, errors that may arise. First of all, experiments with labelled standards were conducted in the research area of Montelibretti (rural station, which is sited about 20 km northeast of Rome), with the purpose of optimizing sampling efficiency. Finally, the method was applied to the analysis of these compounds in the air of a suburban area with small industrial plants in order to evaluate the feasibility of the proposed sampling method system, by comparing concentrations of native compounds acquired during simultaneous daily and weekly sampling. [ABSTRACT FROM AUTHOR]

Residential air cleaners exploiting different technologies re commonly used today to remove air contaminants from indoor environments. Different methods have been developed in the USA and Europe to test their efficiency. The one used in the USA provides a more comprehensive view of indoor processes, because testing is performed in a large simulation chamber (28.5 m3), using anthropogenic emissions, such as cigarette smoke, to generate pollution. Testing rooms are also important to investigate new removal technologies, or to improve them. Since no such testing facilities exist in Italy, one of 12.4 m3 was built in which cigarette smoke, resuspended dust from agricultural soil and, for the first time, diesel exhaust emissions were used to generate indoor pollution. Performances were tested with two air cleaning systems, exploiting completely different removal technologies. Accurate values of decay rates of indoor pollutants were obtained using a suite of on-line and out-of-line monitors for the measurement of particulate matter, volatile organic compounds (VOCs) and some inorganic gases. Proton-transfer mass spectrometry (PTR-MS) provided an almost real-time detection of several VOCs and H2S, at trace levels (0.01 ppbv). A method using a common in vitro bioassay was developed to assess the ability of air cleaners to remove indoor toxic substances. [ABSTRACT FROM AUTHOR]

This study investigated the influence of different charge typologies and additives on the PCDD/Fs amount produced and on the congener profiles in an iron ore sintering plant. Many tests were carried out combining different typologies of charge (iron materials) and solid fuel (“coke breeze” or “anthracite”) with or without the use of urea. The PCDD/Fs produced ranged from 1.2 to 22.7 μg I-TEQ/ton of agglomerate, whereas the PCDD/Fs released to the ambient air ranged from 0.10 to 1.92 ng I-TEQ/Nm3 because of cleaning in an electrostatic precipitator (ESP) and a Wetfine scrubber (WS). A more homogeneous charge with a higher amount of fine particles charge appeared to produce a lower PCDD/Fs concentration due to a better combustion but this hypothesis needs further investigations on charges having different dimension particles. Only a synergitic action of urea and anthracite was able to reduce the high PCDD/Fs content due to the bad combustion of the more inhomogeneous charge with a lower amount of fine particles. The congener profile was a typical combustion process fingerprint because the PCDFs predominated, the highly chlorinated congeners (HeptaCDD and OctaCDD) prevailed in PCDDs, whereas in PCDFs the profile was more varied; 1,2,3,4,6,7,8-HeptaCDF was the main contributor to the total concentration while 2,3,4,7,8-PentaCDF was the main contributor to the I-TEQ concentration. Whereas all the parameters under scrutiny influenced strongly the amount of PCDD/Fs produced, they affected only slightly the fingerprint of PCDD/Fs. In all cases studied, the reduction obtained using urea, anthracite, or the more homogeneous charge with a higher amount of fine particles was slightly greater on the higher chlorinated congeners in respect to the lower ones. [ABSTRACT FROM AUTHOR]

Active carbon-based sorbents are well known and are used in analytical chemistry. Activated carbon fibers (ACFs) are mainly used as abatement systems in industrial emission pollution control. The objective of this study was to extend the use of ACFs in analytical chemistry for the analysis of polychlorodibenzo-p-dioxins (PCDDs), polychlorodibenzofurans (PCDFs), dioxin-like polychlorobiphenyls (PCBs), and chlorobenzenes (CBs). For this purpose, the extraction efficiency was evaluated based on the QA/QC criteria defined by EPA/ISO reference methods on 13C-standards recovery rates. The procedures tested were ultrasonic assisted extraction (UAE), Soxhlet extraction (SE), accelerated solvent extraction (ASE), and microwave-assisted extraction (MAE). Each experiment was performed in triplicate to ensure the repeatability of the results, and a second extraction assessed the complete extraction. The comparison of the results of each set of experiments with the minimum requirements of the reference methods for each class of compounds led to SE being chosen as the best technique. SE with toluene resulted in a reduction of time and costs and with respect to the other investigated techniques. The present work demonstrated that ACFs can be used in environmental fields means of both prevention and control (exploiting the adsorbent characteristics) and for analytical purposes (exploiting the desorption) for the described chlorinated classes of pollutants. [ABSTRACT FROM AUTHOR]

Polycyclic Aromatic Hydrocarbons (PAHs) are typical pollutants arising from incineration. They are produced in any incomplete combustion principally due to inhomogeneities in a combustion chamber. The effects of the afterburning temperature on PAHs formation during sewage sludge incineration are discussed in this paper. Tests were performed inside the area of the wastewater treatment plant of `Bari Ovest' on a demonstrative plant (maximum throughput 250 kg hr-1 of dewatered sludge at 20% solids concentration) equipped with a fluidised bed furnace (FBF) and a rotary kiln furnace (RKF) where sewage sludge was fed, either as it was taken from the dewatering section of the wastewater treatment plant, or previously spiked by different dosages of chlorinated hydrocarbons. Exhaust gases were sampled before the bag filter, where the pollutants can be considered representative of those arising from the process. Parallel sampling of flue gas at the stack was also carried out. In the FBF tests with sludge spiked with high dosages of chlorinated hydrocarbons highest values of PAHs concentrations (>3.9 μg Nm-3) were detected before filtration, when the afterburning chamber was not in use. The operation of the afterburning chamber, at a temperature higher than 900 °C, allows to partially suppress PAHs formation up to values of 0.9–3.2 μg Nm-3. PAHs removal efficiency of the exhaust gas treatment was calculated with a mean value for all the test of 72%. In RKF tests PAHs displayed much lower values before filtration (range 0.04–2.98 μg Nm-3, mean value 0.51 μg Nm-3) probably due to the longer gas residence time in the furnace (>6 s in comparison with values <2 s in fluidised bed furnace). Surprisingly, for RKF tests PAHs removal efficiency of gas treatment appeared quite unstable: some tests evidenced PAHs stripping in the scrubber, where the effluent of the wastewater treatment plant was used. No correlation was observed in RKF tests between PAHs concentration before the bag filter and the temperature of the afterburning chamber. [ABSTRACT FROM AUTHOR]

Ammonia is a common factor linking air in bat caves and air pollution in the proximity of agricultural fields treated with livestock farming sewage and slaughterhouses, where important clusters of COVID-19 have recently been reported all over the world. Such a commonality has a further connection with the known behavior of some viruses of the coronavirus family, such as the murine hepatitis virus, whose spike glycoprotein (S) can be triggered to a membrane-binding conformation at pH 8.0. Within the airborne route of virus transmission, with particular relevance for crowded and enclosed environments, these observations have prompted a hypothesis that may represent a contributing cause to interpret the geographical variability of the virus diffusion and the surging rise of COVID-19 cases in slaughterhouses all over the world. The hypothesis is that, in these environments, the SARS-CoV-2 S protein may find on a fraction of the airborne particles an alkaline pH, favorable to trigger the conformational changes, needed to induce the fusion of the viral envelope with the plasma membrane of the target cells. [ABSTRACT FROM AUTHOR]

Polychlorinated byphenyls (PCBs) are a class of Persistent Organic Pollutants extremely hard to remove from soil. The use of plants to promote the degradation of PCBs, thanks to synergic interactions between roots and the natural soil microorganisms in the rhizosphere, has been proved to constitute an effective and environmentally friendly remediation technique. Preliminary microcosm experiments were conducted in a greenhouse for 12 months to evaluate the capacity of the Monviso hybrid poplar clone, a model plant for phytoremediation, to grow in a low quality and PCB-contaminated soil in order to assess if this clone could be subsequently used in a field experiment. For this purpose, three different soil conditions (Microbiologically Active, Pre-sterilized and Hypoxic soils) were set up in order to assess the capacity of this clone to grow in the polluted soil in these different conditions and support the soil microbial community activity. The growth and physiology (chlorophyll content, chlorophyll fluorescence, ascorbate, phenolic compounds and flavonoid contents) of the poplar were determined. Moreover, chemical analyses were performed to assess the concentrations of PCB indicators in soil and plant roots. Finally, the microbial community was evaluated in terms of total abundance and activity under the different experimental conditions. Results showed that the poplar clone was able to grow efficiently in the contaminated soil and to promote microbial transformations of PCBs. Plants grown in the hypoxic condition promoted the formation of a higher number of higher-chlorinated PCBs and accumulated lower PCBs in their roots. However, plants in this condition showed a higher stress level than the other microcosms, producing higher amounts of phenolic, flavonoid and ascorbate contents, as a defence mechanism. [ABSTRACT FROM AUTHOR]

Drying is a critical point for the exploitation of biomass for energy production. High moisture content negatively affects the efficiency of power generation in combustion and gasification systems. Different types of dryers are available however; it is known that rotary dryers have low cost of maintenance and consume 15% and 30% less in terms of specific energy. The study analyzed the drying process of woody residues using a new prototype of mobile rotary dryer cocurrent flow. Woodchip of poplar (Populus spp.), black locust (Robinia pseudoacacia L.), and grapevine (Vitis vinifera L.) pruning were dried in a rotary drier. The drying cycle lasted 8 h for poplar, 6 h for black locust, and 6 h for pruning of grapevine. The initial biomass had a moisture content of around 50% for the poplar and around 30% for grapevine and black locust. The study showed that some characteristics of the biomass (e.g., initial moisture content, particle size distribution, bulk density) influence the technical parameters (i.e., airflow temperature, rate, and speed) of the drying process and, hence, the energy demand. At the end of the drying process, 17% of water was removed for poplar wood chips and 31% for grapevine and black locust wood chips. To achieve this, result the three-biomass required 1.61 (poplar), 0.86 (grapevine), and 1.12 MJ kgdry solids−1 (black locust), with an efficiency of thermal drying (η) respectively of 37%, 12%, and 27%. In the future, the results obtained suggest an increase in the efficiency of the thermal insulation of the mobile dryer, and the application of the mobile dryer in a small farm, for the recovery of exhaust gases from thermal power plants. [ABSTRACT FROM AUTHOR]