Ash Samples Research Articles

Measurement of Natural Radioactivity in Fly Ash from a Lignite-Fired Thermal Power Plant and Radiological Risk Assessment Using RESRAD Code

In this study, the activity concentrations of natural primordial radionuclides in fly ash (FA) samples collected from the landfill area of Afşin-Elbistan A lignite-fired thermal power plant (AE-A LFTPP) located in Kahramanmaraş province of Türkiye were measured using a gamma-ray spectrometer. Also, the radiological risk was assessed using the Residual Radioactivity Onsite 7.2 code. The average activity concentrations of 226Ra, 232Th and 40K in FA samples varied from 291 ± 10 to 853 ± 25 Bq/kg, 23 ± 1 to 125 ± 4 Bq/kg and 112 ± 10 to 315 ± 18 Bq/kg, respectively. The predicted maximum total annual effective dose rate due to the natural radionuclides and their progenies is 4.7, 4.4, and 4.0 mSv/y at t = 1000 y for 0.5-m, 1.25-m, and 2.0-m cover scenarios, respectively. While the predicted maximum total cancer risk is 4.56 × 10−3 (3.95 × 10−3 for 226Ra, 5.18 × 10−4 for 232Th and 6.14 × 10−15 for 40K), 4.00 × 10−3(3.80 × 10−3 for 226Ra, 1.90 × 10−4 for 232Th and 7.69 × 10−15 for 40K) and 3.71 × 10−3 (3.71 × 10−3 for 226Ra, 1.820 × 10−8 for 232Th and 7.66 × 10−15 for 40K) at t = 1000 y for 0.5-m, 1.25-m and 2.0-m cover scenario, respectively. Results also revealed that the total doses and cancer risks are less in thicker cover scenarios throughout the 1000 y time span and that 226Ra is the major contributor to the risk in all the scenarios owing to its higher activity concentration than 232Th and 40K.

Relevance of using portable X-ray fluorescence to identify gold hyperaccumulator plants

Field Portable X-Ray Fluorescence (FPXRF) was investigated as an alternative analysis tool for the detection and quantification of gold in hyperaccumulator plants in the field. First, synthetic gold standards were prepared with materials chosen to best simulate plant material, using microcrystalline cellulose (mcc) or ash by adding known amounts of gold. Powder samples were obtained containing gold in amounts ranging from 10 to 1000 ppm of gold. They were analysed, as well as blank samples of mcc and ash, using a NITON xl3t GOLDD+ FPXRF spectrometer in AllGeo and Soil modes with an analysis time of 60 s. Results were compared to Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES) analysis of the synthetic gold standards after digestion in aqua regia. Gold was detected and accurately quantified in synthetic gold standards containing more than 25 ppm of gold in AllGeo mode. At lower concentration, results were much more inaccurate, with no gold being detected at 10 ppm. In Soil mode, similar results to AllGeo mode were obtained with mcc synthetic standards. However, with ash synthetic standard gold quantification was very poor over the whole concentration range and gold was detected in the blank ash sample, which was confirmed as a false positive by the subsequent ICP analysis. Samples of Phyllanthus stipulatus, suspected gold hyperaccumulators, collected on gold-bearing sites in French Guiana were then analysed following the same protocol. The same false positive phenomenon was observed in some of them, with gold being detected by FPXRF in Soil mode but not by ICP analysis. Furthermore, analysis of the FPXRF spectra revealed that none of the characteristic gold emission ray was present. This false positive was attributed to an interference caused by zinc, present in significant amount in the ash of the synthetic standard and the collected plants.

Mineralogy and geochemistry of rare metal (Zr-Nb-Hf-Ta-REE-Ga) coals of the seam XXX of the Izykh Coalfield, Minusinsk Basin, Russia: Implications for more widespread rare metal mineralization in North Asia

This study focuses a comprehensive mineralogical and geochemical study of rare-metal (Zr-Nb-Hf-Ta-REE-Ga) mineralization in the Permian coal seam XXX-XXXa of the Izykh Coalfield, Minusinsk Basin, southern Siberia. A link is demonstrated between the accumulation of rare metals in the coal with a volcanogenic rock parting up to 45 cm thick separating the coal seams. The floor of seam XXX is also characterized by the presence of pyroclastic material, which affects the level of accumulation of rare elements in the coal of the seam. Coals and intra-seam rock partings in seam XXX-XXXa have abnormally high concentrations of Zr, Nb, Hf, Ta, REE and Ga. In coal ash samples, the contents of some elements are highly evaluated, e.g., 1.4% Zr, 0.26% Nb, 164 ppm Hf, 17.9 ppm Ta, 0.8% REE, 0.13% Y, and 226 ppm Ga. The concentration of rare elements is higher in the coal and coal ash of the XXX coal seam than in the XXXa coal seam. The accumulation of anomalous concentrations of Zr-Nb-Hf-Ta-REE and Ga is mostly specific for the rock parting between the XXX and XXXa seams, as well as for the coals in contact with this parting. Zirconium, Nb, Y, and REE form more contrasting halos near the parting compared to Ta, Hf, and Ga. This is explained by the different mobility of the elements under weathering and diagenetic conditions. Other ore elements are concentrated to a greater extent in the coal in the near-contact zone, as well as at a distance from the partings. Ore material is concentrated primarily in the fine-dispersed mineral phase represented mainly by Zr-Nb-Ti-Fe oxides, complex Nb-Zr-P silicates, and REY-bearing phosphates (monazite, xenotime). Volcanogenic pyroclastics of acidic and alkaline composition (rhyolite-pantellerite) influenced the accumulation of rare metals in coal. Volcanic ash, transported from a distant source, served as the raw material for the formation of the rock interlayer in coal. The composition of this volcanic ash is believed to correspond to a pantelleritic tuff. These findings are comparable to those reached in earlier work on the altered ash in the coal seam XI of the Kuznetsk Coal Basin, which has similar geochemical features and is also of Permian age. Complex Zr-Nb-Hf-Ta-REE-Ga mineralization in the coals of the Kuznetsk and Minusinsk basins, associated with volcanogenic pyroclastics, indicates a wide manifestation of active acid and alkaline volcanism during the formation of coal deposits and the possibility of identifying similar mineralization in Permian coals of East and North Asia.

Radiation impact of ashes from the combustion of bottom sediments in a municipal sewage treatment plant, Czajka, located in Warsaw, Poland

Abstract The aim of the present research was to assess the radiological importance of the fly ashes generated from the incineration of sludge from the “Czajka” sewage treatment plant located in Warsaw, Poland. The γ-spectrometry technique was employed for their radiometry. The high purity germanium (HPGe) detector was mathematically energy-efficiency calibrated. The ash samples were measured two times, i.e., after 24 days and after 3 months of storage. Storage was supposed to provide a radioactive equilibrium. Radionuclides from three natural decay series, i.e., uranium–radium, uranium–actinium, and thorium, were detected in the ash samples. Apart from these, 40K, 137Cs, and 7Be were also detected. The indicated levels of radionuclides do not produce radioactive hazards, regardless of the method used for further management.

Ash Properties and Environmental Impact of Coal and Its Blend with Patent Fuel for Climate Sustainability

Fossil fuels are still widely used today, and exploring more sustainable ways of using coal is crucial. One promising approach is to develop a patented fuel with reduced harmful gas emissions during combustion. This study aims to investigate the properties of the ash produced by burning steam coal mixed with various ratios of patent fuel. The combustion process was carried out using a standard solid fuel boiler with a power output of 70 kW. The ash samples were analyzed using various analytical methods, and ash leaching tests were conducted. The study found that adding patent fuel to coal affects combustion and ash composition. Determining the thermal stability of ash samples showed that adding patent fuel to coal results in decomposition starting earlier and in stronger combustion. The ash produced by patent fuel–coal mixtures contains lower concentrations of Ba, Cr, Ga, Li, Mn, V, and Zn than pure coal combustion. Leaching tests showed that coal ash leachates had higher concentrations of environmental pollutants, such as As, Cd, Co, Mn, Mo, Sb, and U, than patent fuel leachates. Adding patent fuel to coal affects combustion, ash properties, emissions, and disposal. Understanding these implications can help to develop sustainable coal usage and reduce environmental impact.

Modeling of Unburned Carbon in Pulverized Coal-Fired Supercritical Steam Generators

ABSTRACT In coal-fired boilers, one of the most important metrics for optimizing combustion is the proportion of unburned carbon (UC) in the ash. In most Indian power plants, it is still assessed offline through manual sample collection and laboratory analysis. The laborious processes of sample collection, preparation, analysis, and reporting require at least five to eight hours of work. The delayed results may not be useful to optimize combustion in the boiler furnace, as the boiler operating conditions may be completely different from the conditions when the samples were collected. Instead, the use of prediction algorithms may bring timely corrective action if the UC goes high. The present experimental study is taken up to obtain a correlation between UC and corresponding relevant boiler operational parameters and on the residence time of coal particles in the boiler furnace. Multiple regression analysis is performed using ANOVA tools. One hundred and ninety-four sets of coal, ash samples and boiler operating parameters are collected from 07 supercritical units. Coal proximate, coal fineness and ash UC analysis are carried out. The analyzed results and collected boiler operational data are statistically analyzed using Microsoft Excel’s ANOVA tool to understand the dependent behavior of UC on the boiler operational parameters and fired coal characteristics. The empirical equations are proposed for the prediction of UC in bottom and fly ash for supercritical boilers. Additionally, fresh 20 sets of coal, ash samples, and related operating data are gathered for the validation of the proposed empirical equations. For additionally collected samples, the predicted results are compared with the offline measured laboratory results. The maximum deviation between the predicted and laboratory results are within the range of ± 0.40% and ± 0.24% for bottom and fly ash samples, respectively.

Direct carbonation of porous materials produced from self-hardened paper mill fly ash

A high-Ca fly ash generated from a paper mill using a fluidized bed boiler was used as the potential medium to sequester CO2 via the direct carbonation process. In this study, the fly ash samples were exposed to accelerated carbonation to produce hardened pastes. The influence of the porosity controlled by the amount of foam in the matrix for maximizing CO2 sequestration was determined. The effect of porosity on carbonation was evident. The samples prepared with 40 % foam and a water-to-fly ash ratio of 0.79 recorded porosities of 56.1 % (carbonated) and 66.8 % (naturally carbonated (NC)) with the lowest mechanical strength of 2.1 and 1.1 MPa, respectively. These naturally carbonated (NC) samples have been cured naturally without using high CO2 pressure. Meanwhile, the samples prepared with 10 % foam and a water-to-fly ash ratio of 0.5 recorded porosities of 41.1 % (carbonated) and 52.9 % (NC) with the highest strength at 10.2 and 4.6 MPa, respectively. The highest carbonation efficiency determined by thermogravimetric analysis was obtained from the carbonated samples with 40 % foam. Scanning electron microscopy–energy-dispersive spectroscopy depicted the areas with high Al/Si content but low Ca–O content (dark areas) and carbonated areas with high Ca–O content (bright areas). Mercury intrusion porosimetry was used to determine the pore size distribution, whereby the samples were dominated by large capillary pores, resulting in their high porosity in this study.

Emission and distribution characteristics of PCDD/Fs during the co-processing of various solid wastes in coal-fired boilers in China

The advancement of co-processing solid wastes in coal-fired boilers is significant for waste recycling and contributes to the sustainable development of the coal-fired power industry. However, concerns over the emission of dioxins during co-processing have prompted a comprehensive investigation into the dioxin emission properties. In this study, the PCDD/F emission concentrations of seven coal-fired boilers, including three pulverized coal boilers and four circulating fluidized bed boilers were examined. The results indicate that co-processing solid wastes in coal-fired boilers did not lead to an increase in the mass concentration of dioxins in either the flue gas or solid samples, and the international toxic equivalents (I-TEQ) of dioxins in the flue gas complied with prevailing emission standards (0.1 ng I-TEQ/Nm3) in China, proving that coal-fired boilers co-processing would not raise the emission risk of dioxins. The types of waste during co-processing had minimal effect on the I-TEQ of dioxins. A significant proportion of PCDD/Fs was observed in the ash samples, while only 13.0–25.7% and 0.7–6.8% of dioxins were distributed in the boiler slag and the flue gas, respectively. The emission factor of dioxins under the blank conditions ranged from 0.009 to 0.327 ng I-TEQ/kg-coal, while it ranged from 0.015 to 0.129 ng I-TEQ/kg-(coal+waste) under the co-processing conditions. The reduction of emission factor under co-processing condition could be attributed to the significant decrease of dioxins I-TEQ.

Co-gasification of lignite and spent tea waste for the generation of hydrogen-rich syngas in a fluidized bed gasifier

The co-gasification of high moisture and high volatile content low-rank lignite (LG) coal and a common waste generated from the brewed tea leaves was studied in a fluidized bed gasification unit. Multiple experiments were conducted at different temperatures, ranging from 800 °C to 900 °C, at fixed operating parameters to elucidate the catalytic thermo-chemical impact on the gasifier performance parameters. The catalytic effect of alkali and alkaline earth metals (AAEMs), especially CaO, K2O, and Na2O present in the spent tea waste (STW) sample, on the product gas composition and performance parameters during the co-gasification experiments with LG was demonstrated. Mixed blends of LG and STW showed enhancement in the overall reactivity of the steam gasification runs, compared to the LG-only feed, primarily due to the change in the surface morphology, textures, and pore structures of the solid product ash samples, as identified with the electron spectroscopy analysis. Liquid and product samples were analyzed using characterization techniques such as Fourier transform infrared (FTIR) spectroscopy, thermogravimetric analysis (TGA), X-ray diffraction (XRD), and scanning electron microscopy-energy dispersive X-ray analysis (SEM-EDX) analytical techniques, along with the proximate, ultimate, and X-ray fluorescence (XRF) analysis of the gasification feed samples. An optimized blend ratio of 20 wt % of STW with LG sample enhanced the volumetric gas composition of H2 and CH4 gases from 52.03 % to 61.32 % and 3.98 %–5.45 % (on a dry-N2-free basis) with a relatively constant CO gas composition. It showed a reduced CO2 composition from 28.64 % to 18.25 % (on a dry-N2-free basis) for the gasification temperature of 900 °C. Even at the lower gasification temperatures of 800 °C and 850 °C with LG + STW feed, steam gasification experiments showed relatively comparable or superior performance to gasification experiments at 900 °C with LG-only feed. The present study indicated a holistic way to utilize the spent tea waste generated from millions of homes and commercial establishments in various parts of the world with potential application towards synergistic gasification process with other conventional carbon-source materials.

Volcanic Glass as a Proxy for Paleotopography Suggests New Features in Late-Miocene Oregon

Volcanic glass has been used extensively as a paleoaltimeter. Deuterium (2H) concentrations in glass have been found to be stable over geologic timescales, making δ2H (also known as δD) a reliable proxy for ancient water chemistry. However, continued work revolves around better understanding how different factors affect preserved water in volcanic ash. Here, we analyze δD in the Rattlesnake Tuff (RST), a widespread ca. 7 Ma ash-flow tuff, and create a paleoisoscape to assess variations in δD across Oregon during that time. To this end, 16 ash samples were collected across central and eastern Oregon from various flow units within the RST. Samples were analyzed for δD using a temperature conversion elemental analyzer (TC/EA) connected to a mass spectrometer and elemental composition using a scanning electron microscope (SEM). We compared the isotopic results to modern water and published ancient water proxy data to better constrain changes in climate and topography across Oregon throughout the Neogene. We also estimated wt. % H2O by calculating excess (non-stoichiometric) oxygen from SEM elemental data. We did not observe significant variations in δD among the flow units from single locations, nor was there a significant relationship between the prepared glass shard composition and wt. % H2O or δD, supporting the use of volcanic glass as a reliable paleoenvironmental indicator. Our results show significant spatial variation in δDwater values of RST, ranging from −107‰ to −154‰. δD values of ancient glass were similar to modern water near the Cascade Mountains but became relatively negative to the east near the inferred eruptive center of the RST, suggesting that a significant topographic feature existed in the vicinity of the RST eruptive center that has since subsided.

Unintentional persistent organic pollutants in cremation process: Emissions, characteristics, and inventory

Pollutants produced by cremation furnaces have gradually caused concern because of the increasing rate of cremation around the world. In this study, the levels, patterns, and emission factors of unintentional persistent organic pollutants (UPOPs) from cremation were investigated. The toxic equivalent (TEQ) concentrations (11 % O2 normalized) of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) in flue gas ranged from 0.036 to 22 ng TEQ/Nm3, while the levels of polychlorinated biphenyls (PCBs) and polychlorinated naphthalenes (PCNs) in flue gas samples ranged from 0.0023 to 1.2 ng TEQ/Nm3 and 0.17–44 pg TEQ/Nm3, respectively. The average concentrations of UPOPs in flue gas from car-type furnaces were higher than those from flat-panel furnaces. Secondary chambers and air pollution control devices were effective for controlling UPOPs emissions. However, heat exchangers were not as effective for reducing UPOPs emissions. It was observed that the UPOPs profiles exhibited dissimilarities between fly ash and flue gas samples. HxCDF, OCDD, and PeCDF were the dominant homologs of PCDD/Fs in flue gas, while HxCDF, PeCDF, and HpCDF were the dominant homologs in fly ash. The fractions of MoCBs and MoCNs in fly ash were higher than those in flue gas. Finally, we conducted an assessment of the global emissions of UPOPs from cremation in the years of 2019 and 2021. The total emission of UPOPs in 47 countries was estimated at 239 g TEQ in 2021, which was during the peak period of the COVID-19 pandemic worldwide. The emissions in 2021 increased by approximately 24 % compared to 2019, with the impact of COVID-19 being a significant factor that cannot be disregarded.

Determination of Concentration of Heavy Metals in Wood Ash

Heavy Metals such as lead, chromium, and arsenic are thought to be present in wood ashes. As many people use wood ash in gardens, we decided to test how easily these metals can be extracted from wood ash. Metals were extracted from 10-gram samples of ash by mixing with 100 ml of 2.0% trace metal nitric acid, gravity filtering, and final filtering with a 0.22 um. nylon syringe. Absorption data for the extracted samples was compared to a calibration curve of absorption versus concentration constructed from data obtained with a Shimadzu AA7000. Initial results indicate that the concentration of the metals are below the lower limit of detection for Cr, As, and Pb which are 0.2 ppm, 2.0 ppm, and 0.5 ppm respectively. However, the laboratory-fortified matrix sample for each metal failed, thus we will need to perform standard addition tests to certify these results. This work was supported by NASA WV Space Grant Consortium training grant number 80NSSC20M0055.

New measurements of the hemispherical albedo of cometary analogues: Influence on the amplitude of the change of cometary brightness during its outburst

The paper presents new experimental results of measurements of the hemispherical albedo of a potential comet analogue and an analysis of its influence on the change in the cometary brightness. Measurements of the spectral properties of the tested analogues were performed using a Cary 5000 spectrometer in the wavelength range from 200 to 2500 nm. Two samples were used as a dust analogue: a mixture of sand and ash (sample A) and a mixture of sand and charcoal (sample B), respectively. The obtained hemispherical albedo values for the tested samples ranged from 1.20% to 32.25%. In particular, for sample B, the obtained hemispherical albedo values are comparable to the actual reflectance for comet 67P. Based on the obtained spectral properties of the tested samples, a thermodynamic model of cometary activity was developed and used, among others, to calculate the power absorbed by the tested analogue and the sublimation flux occurring through the porous structure of the fine-grained dust present on the cometary surface. The obtained results were used to calculate the change in the cometary brightness during its outburst, the upper limit of which was equal to 5.36 magnitude.

Characterisation of rare earth element-bearing mineral phases present in South African coal ash using Mineral Liberation analysis

Critical raw materials, including rare earth elements (REE), are the cornerstone of modern technologies. Due to their unique properties, REE are in high demand, leading to the exploration and research of alternative sources. Coal combustion by-products, specifically coal ash, has been identified as a potential alternative source of REE, but more research is required. This study aimed to identify REE’s occurring in power station and laboratory-derived coal ash. Results from Inductively Coupled Plasma-Mass Spectrometry (ICP-MS) and Mineral Liberation Analysis are presented herein, to gain insight into rare-earth-bearing minerals occurring in the ash samples.REEs were determined in both sets of ash samples at values higher than 600 parts per million (ppm) using ICP-MS. Critical REE occur in ranges from 203 to 406 ppm; uncritical REE from 179 to 256 ppm; and excessive REE ranging from 197 to 348 ppm in these samples. Laboratory-derived coal ash and power station-generated ash samples were prepared as polished blocks and coated for examination using a Mineral Liberation Analyser (MLA). A bright phase search mode was employed to detect rare earth-bearing mineral phases using the back-scattered electron detector (BSE).Energy dispersive spectroscopy (EDS) was used to determine elemental compositions in these phases.Four rare earth-bearing mineral phases were determined, namely: monazite-REE, xenotime-REE, Ce-REErium rich, and REE-silicate. The laboratory-derived ash samples had a greater proportion of liberated rare earth-bearing minerals, related to the lower proportion of aluminosilicate glassy phase, related to the low temperature ashing procedure.The detailed mineralogy provides insight into the design of REE extraction processes, targeting specific REE’s hosted in the various minerals. This will be documented in a future paper.

Agglomeration behaviour of various biomass fuels under different air staging conditions in fluidised bed technology for renewable energy applications

The most common technology for thermochemical conversion of solid fuel through the process of gasification, such as coal, varieties of residues from biomass and agriculture are the bubbling fluidised bed or fluidised bed systems. However, there are some disadvantages within these systems including the formation of eutectic mixtures, increased process of melting and bed agglomeration. Hence, the current study aimed to evaluate the agglomeration behaviour of various biomass fuels. Characteristics of five biomass fuels (miscanthus, peanut, straw, domestic wood and industrial wood) in a bubbling fluidised bed (BFB) combustor were studied by SEM-EDX, XRD and XRF analysis of bed materials and ash samples. The influence of bed temperatures on the fuel ash composition and bed particles was evaluated, as well as fuel ash components, their interaction with the particles from the bed sand and morphology of the bed material. The combustion efficiency ranged from 95.5 to 99.5% with the highest value obtained for miscanthus under SA conditions. The peanut and straw had the highest K content, whereas the industrial wood ash contained the highest Ca content compared to other biomasses. The XRF results showed that most of the potassium (K) from the wheat straw biomass was converted to K2O with 19%. No bed agglomeration was noticed without staging-air (WSA) and with staging-air (SA) combustion conditions, even with temperatures up to 850 °C during the testing period. Overall obtained results demonstrated that agglomeration is unlikely expected to be a major problem during fluidised bed combustion of tested biomass fuels.

Leachability of hexavalent chromium from fly ash-marl mixtures in Sarigiol basin, Western Macedonia, Greece: environmental hazard and potential human health risk

Hexavalent chromium (Cr (VI)) is an environmental contaminant brining high concerns due to its higher toxicity and mobility in comparison with trivalent chromium Cr(III). Cr (VI) has been linked with several adverse health effects, including respiratory diseases, lung cancer, and skin irritation. The primary sources of it in the environment are industrial activities.Most of the time, fly ash made of lignite can release Cr(VI) when it comes into contact with water in an aquatic environment. The objective of this study is the investigation of Cr (VI) concentration in leachates of fly ash and marl mixtures and the determination of its solubility under different pH conditions. Samples of fly ash were collected from the Power Plant of Agios Dimitrios. Additionally, samples of marl were collected from the mine of South Field, and both samples were mixed and prepared in in different proportions (% w.t.). The leaching experiments were carried out according to the EN-12457/1-4 (2003) standard under different pH conditions and chemical analysis of the leachates were performed by spectrophotometry with diphenylcarbazide (DPC). The environmental footprint of Cr (VI) in the study area was significant, especially in mixtures containing higher concentrations of fly ash. A critical pH range between 6 to 12 is observed. At acidic pH values, a high release of Cr (VI) was observed, while at the mentioned critical values (pH 10–12), a gradual decrease in its leachability was noticed. The high concentrations of Cr (VI) in the industrial area studied require immediate actions in terms of managing and limiting the potential hazardous impacts on the environment and by extension on the public health by developing appropriate prevention strategies.Graphical abstract

EXPLORING THE POTENTIAL OF RED ASH AND MARBLE CHIPS AS ALTERNATIVES IN BASE COURSE MATERIAL VIA BLENDING WITH CRUSHED STONE AGGREGATE

Despite its abundance, red ash has compaction issues owing to its lightweight, rough circular surface, and high porosity. The usage of conventional base course materials across the country incurs shipping expenses and takes time, slowing down projects because they are only widely available in limited areas across the country. In this study, non-probably sampling approach was used to examine the potential for employing red ash and marble chips as an alternative base course material by mixing them with crushed stone aggregate (CSA). In order to accomplish the goal of this study, an experimental test was conducted via trial and error, focusing on the mechanical stabilization of red ash and marble chips. Their physical characteristics were subsequently assessed through laboratory testing. In the laboratory, nine (9) samples of red ash and marble chips blended with CSA in varying percentages (0, 5, 10, 15, 20, 25, and 30 percent) were examined. The laboratory test results showed that 100% red ash and marble chips gave; CBR, SG, AIV, ACV, LAA, FI, EI, water absorption, and soundness: 55.4%, 2.38%, 18.20%, 26.34%, 19.69%, 5.59%, 12.09%, 2.5% and 13.80 and 83.6%, 2.63%, 19.70%, 26.41%, 19.75%, 23.2%, 16.9%, 1.24% and 12.22 respectively. Several of these test results align with the Ethiopian Road Authority (ERA) standard specifications; however, the findings from the CBR, water absorption, and soundness tests do not. Thus, mechanical stabilization was employed to improve the samples' physical characteristics. Experimental results are obtained by mixing 20% red ash, 20% marble chips, and 60% CSA. The values for CBR, SG, AIV, ACV, LAA, FI, EI, water absorption, and soundness are 102.5%, 2.55, 14.23%, 19.84%, 7.92%, 18.61%, 20.77%, 0.83%, and 7.38, respectively. The CBR, water absorption, and soundness characteristics all meet the necessary ERA standard specifications for crushed weathered rock (GB2) and natural coarsely graded granular materials (GB3) at this particular proportion. Hence, it is recommended to incorporate red ash up to 20% and marble chips up to 20% by weight, alongside 60% CSA, for constructing road base courses, particularly when these materials are reasonably accessible from construction sites and are widely available in the area.

Evaluation on Properties of Cement Mortar and Brick Using Magnetically Separated Coal Power Plant Bottom Ash

Recycling of abandoned waste bottom ash has been a key issue in Republic of Korea in terms of environmental protection as well as economic concern. In this work, a method for recycling of abandoned bottom ash has been discussed based on the results from laboratory and industrial-scale experiments. Abandoned bottom ash was magnetically separated and properties of magnetically separated bottom ash samples as well as properties of mortar and masonry cement brick made of bottom ash were investigated. According to the experimental results, bulk and skeletal densities were ranked in the order of strongly magnetic > weakly magnetic > as-received > non-magnetic (from heavier to lighter) bottom ash. From laboratory-scale experiments, compressive strengths of mortars made of bottom ash samples (measured by ASTM C 109) were lower than that of mortar made of standard sand. Among bottom ash samples, mortar made of non-magnetic bottom ash (after removal of unburnt carbon) showed higher compressive strength with lower thermal conductivity (measured by ASTM C 1113) and weight than others. Masonry cement brick made of magnetic bottom ash showed lower weight and thermal conductivity than those made of standard sand, while meeting the KS strength guideline as a masonry cement brick. The results suggest the applicability of bottom ash as lightweight aggregate for production of masonry cement brick. However, considering the lower strength obtained from masonry cement brick made of as-received bottom ash (without removal of unburnt carbon), unburnt carbon content should be removed prior to its utilization as lightweight aggregate.

Sources, accumulation levels and environmental hazard of heavy metals and metalloids in soils and PM10 fractions of Severobaykalsk

Relevance. The need to study the ecological state of the soil cover of industrial cities, which is the main depositing environment for technogenic emissions of heavy metals and metalloids, to identify the geochemical characteristics of the region and assess the impact on public health. Aim. To assess the sources and accumulation of heavy metals and metalloids in soils and their fraction PM10 in Severobaikalsk and to assess the risks associated with them for public health. Methods. Total content of Zn, As, Cd, Pb, Cr, Co, Ni, Cu, Sb, Mo, V, W, Sr, Bi in soil, coal and ash samples was determined by mass spectral and atomic emission methods with inductive-coupled plasma. Geochemical (KK, Kc, Zc), sanitary and hygienic (Ko) indicators were used. Health risks for adults and children were assessed. Principal component analysis was used. Results. In Severobaikalsk, the priority soil pollutants are Sb, Cu, Pb, Mo, Cr. The soils and their PM10 fraction in the transport zone, where Sb, Cu, Pb, Co, V, W, Ni are accumulated, are the most polluted. The greatest influence on the chemical composition of urban soils and PM10 particles is exerted by emissions from railway infrastructure and coal combustion at the Central Thermal Power Plant (22% for soils in general and 48% for the PM10 fraction). The average total level of contamination of urban soils and PM10 fraction corresponds to a low, non-hazardous level (Zc=6). The total non-carcinogenic risk of soil particles contaminated with heavy metals and metalloids. entering the body of children, exceeded the safe level 1 (from 1.60 in a residential one-story zone to 1.81 in a transport zone). For the adult population, HI values were below the acceptable threshold value. For adult health, there is no carcinogenic risk associated with ingestion or skin contact of As, Cr and Pb. For children, a dangerous risk (ILCRingest 5.56*10–4) of ingestion of carcinogenic heavy metals and metalloids was identified.

Promotion of chloride removal from MSWI fly ash by an accelerated wet-carbonation process to enhance ash recycling in cement manufacture

Chlorides, sulfates, and heavy metals are the three main factors preventing the recycling of municipal solid waste incineration (MSWI) fly ash as an alternative material for cement clinker production, of which chloride plays the main role due to its extremelly hign content in fly ash. This study evaluated three wet-based pretreatment methods (water-washing, CO2-aided washing, and flue gas-aided washing) to remove chlorides using MSWI fly ashes from 13 incineration plants in China. Water washing was suitable for removing Cl- from MSWI fly ash containing a limited amount of less-soluble Cl-containing salts (Ca(OH)Cl, Ca2Al(OH)6(H2O)2Cl, and Ca6(CO3)2(OH)7Cl). However, for fly ash with a significant proportion of these less-soluble Cl-containing salts, injection of CO2/flue gas during washing promoted their decomposition and increased the chloride removal rates by 2–12%. Compared with chloride, the removal rate of sulfate was lower under all treatment scenarios and ranged from 7% to 47%. Therefore, caution should be taken when exploring techniques for the deep removal of chloride from MSWI fly ash, as sulfates may be the limiting factor in fly ash samples with low chloride contents when utilizing the fly ash for cement clinker production. Heavy metals in fly ash were not a limiting factor for any ash samples (either raw ash or treated ash) when utilizing the fly ash for clinker production. However, the dissolution of heavy metals in the washing solution deserves more attention, as a large amount of wastewater will be generated during wet-based pretreatment methods. This study confirmed that CO2/flue gas injection during washing promoted the removal of the less-soluble harmful components of fly ash, expanding the applications of ash materials.