Two fly ashes from municipal solid waste incineration were selected to study their heavy metal leaching behavior. The main purpose of this research is to investigate the characteristics of fly ashes and compare the leaching of heavy metals in different leaching environment. pH and acid neutralization capacity analysis showed that fly ashes were highly alkaline. Fly ashes also contained a variety of heavy metals including Pb, Cu, Cr, Zn, Cd and Ni etc. Leaching studies showed that the alkalinity of fly ashes raised the pH of leaching solution from acidic to basic. Ni, Cu and Zn were strongly bound to ashes and manifested low leaching. In contrast, Cr and Cd had high mobility but their leaching was inhibited by the low solubility of carbonate Cr and Cd. Pb was highly leachable in the alkaline environment with concentration in the leaching solution reached as high as 9.74 mg/L. In addition, the presence of EDTA in the environment also increased leaching. Pb concentration was raised to 16.63 mg/L. This could be attributed to the chelating capacity of EDTA which means that the presence of organics in natural environment should be taken into consideration.

Although the Indian population is largely vegetarian, not much attention has been given to the cultivation of vegetables, as compared to other crops like cereals, pulses and oil seeds. Therefore, the present study was conducted on two leafy vegetables, spinach (Spanacia oleracea L.) and methi (Trigonella foenum graecum L.) commonly grown in Aligarh, as the two popular vegetables of Indian diet. The study was conducted for two successive years and during the first year, phosphorus and fly ash interactions with a uniform dose of nitrogen and potassium on both vegetables was observed. During the second year, while keeping nitrogen and phosphorus uniform, potassium and fly ash combinations were studied again with both vegetables, to determine the optimum dose of inorganic fertilizers and fly ash combination. It was observed that fly ash applied at the rate of 15 t ha-1 along with N40P15K20, proved optimum for spinach while in the case of methi, N20P30K40 + FA10 was sufficient. Therefore, both vegetables can safely be grown with 10 to 15 t ha-1 of fly ash and a comparatively lower quantity of NPK.

International audience | Amphibians are now recognized as the most endangered group. One of this decline causes is the degradation of their habitat through direct contamination of water, soil leaching, or runoff from surrounding contaminated soils and environments. In the North of France, the extensive industrial activities resulted in massive soil contamination by metal compounds. Mineral amendments were added to soils to decrease trace metal mobility. Because of the large areas to be treated, the use of inexpensive industrial by-products was favored. Two types of fly ashes were both tested in an experimental site with the plantation of trees in 2000. Aim of the present work was to investigate the effects of extracts from metal-contaminated soils treated or not for 10 years with fly ashes on Xenopus laevis oocyte using cell biology approaches. Indeed, our previous studies have shown that the Xenopus oocyte is a relevant model to study the metal ion toxicity. Survival and maturation of oocyte exposed to the soil extracts were evaluated by phenotypic approaches and electrophysiological recordings. An extract derived from a metal-contaminated soil treated for 10 years with sulfo-calcic ashes induced the largest effects. Membrane integrity appeared affected and ion fluxes in exposed oocytes were changed. Thus, it appeared that extracted elements from certain mineral amendments used to prevent the mobility of metals in the case of highly metal-contaminated soils could have a negative impact on X. laevis oocytes.

Airborne fine particles can affect climate change and human health; moreover, they can be transported over significant distances. However, studies on characteristics of individual particles and their morphology, elemental composition, aging processes, and spatial distribution after long-range transport over the Yellow Sea are limited. Therefore, in this study, we conducted shipborne measurements of fine particulate matter of less than 2.5 μm in diameter (PM₂.₅) over the Yellow Sea and classified the individual particles into seven types based on their morphology and composition. Overall, the percentage of organic-rich particles was the highest, followed by that of sea spray, sulfur-rich, dust, metals, fly ash, soot, and other particles. Near Shandong, China, the percentage of fly ash and sulfur-rich particles increased, while an increased percentage of only sulfur-rich particles was observed near the Korean Peninsula. In the open sea, the PM₂.₅ concentrations were the lowest, and sea spray particles predominated. During the cruises, three types (Types 1, 2, and 3) of events with substantially increased PM₂.₅ concentrations occurred, each with different dominant particles. Type 1 events frequently featured air masses from northern China and Mongolia with high wind speeds and increased dust particles. Type 2 events involved air masses from China with high wind speeds; fly ash, soot, organic-rich particles, and the sulfate percentage in PM₂.₅ increased. Type 3 events displayed stagnant conditions and local transport (from Korea); soot, dust particles, and the secondary sulfate and nitrate percentages in PM₂.₅ increased. Thus, different types of transport affected concentrations and dominant types of fine particles over the Yellow Sea during spring.

Lead (Pb) is a toxic metal in industrial production, which can seriously threat to human health and food safety. Thus, it is particularly crucial to reduce the content of Pb in the environment. In this study, raw fly ash (FA) was used to synthesise a new active silicate materials (IM) employing the low-temperature-assisted alkali (NaOH) roasting approach. The IM was further synthesised to form zeolite-A (ZA) using the hydrothermal method. The physicochemical characteristics of IM and ZA amendments before and after Pb²⁺ adsorption were analysed using the Scanning electron microscope-Energy Dispersive Spectrometer (SEM-EDS), Fourier Transform infrared spectroscopy (FTIR), and X-ray diffraction (XRD) apparatuses. The results revealed the considerably change in the microstructure and functional groups of IM and ZA amendments, conducive to Pb²⁺ removal. Moreover, a 3-year field experiment revealed that the IM and ZA significantly improved the growth of rice and reduced available Pb by 21%–26.8% and 9.7%–16.9%, respectively. After 3 years of remediation, the Pb concentration of the rice grain reached the national edible standard (≤0.2 mg kg⁻¹) of 0.171 mg kg⁻¹ and 0.179 mg kg⁻¹, respectively. Meanwhile, the concentration of acid-exchangeable Pb reduced, while those of reducible and residual fractions of Pb increased. There was no significant difference between the IM and ZA treatments. The potential mechanisms of remediation by the amendments were ion-exchange, complexation, precipitation, and electrostatic attraction. Overall, the results indicate that IM is suitable for the remediation of contaminated soil and promotes safe food production, and develops an environmentally friendly and cost-effective amendment for the remediation of polluted soil.

This study focused on the syngenetic control of polychlorinated-ρ-dibenzodioxins and dibenzofurans (PCDD/Fs) and heavy metals by field stabilization/solidification (S/S) treatment for municipal solid waste incineration fly ash (MSWIFA) and multi-step leachate treatment. Modified European Community Bureau of Reference (BCR) speciation analysis and risk assessment code (RAC) revealed the medium environment risk of Cd and Mn, indicating the necessity of S/S treatment for MSWIFA. S/S treatment significantly declined the mass/toxic concentrations of PCDD/Fs (i.e., from 7.21 to 4.25 μg/kg; from 0.32 to 0.20 μg I-TEQ/kg) and heavy metals in MSWIFA due to chemical fixation and dilution effect. The S/S mechanism of sodium dimethyldithiocarbamate (SDD) and cement was decreasing heavy metals in the mild acid-soluble fraction to reduce their mobility and bioavailability. Oxidation treatment of leachate reduced the PCDD/F concentration from 49.10 to 28.71 pg/L (i.e., from 1.60 to 0.98 pg I-TEQ/L) by suspension absorption or NaClO oxidation decomposition, whereas a so-called “memory effect” phenomena in the subsequent procedures (adsorption, press filtration, flocculating settling, slurry separation, and carbon filtration) increased it back to 38.60 pg/L (1.66 pg I-TEQ/L). Moreover, the multi-step leachate treatment also effectively reduced the concentrations of heavy metals to 1–4 orders of magnitude lower than the national emission standards. Furthermore, the PCDD/Fs and heavy metals in other multiple media (soil, landfill leachate, groundwater, and river water) and their spatial distribution characteristics site were also investigated. No evidence showed any influence of the landfill on the surrounding liquid media. The slightly higher concentration of PCDD/Fs in the soil samples was ascribed to other waste management processes (transportation and unloading) or other local source (hazardous incineration plant). Therefore, proper management of landfills and leachate has a negligible effect on the surrounding environment.

Coking is a substantial source of carbonaceous aerosols in China, but the emission characteristics and pollution levels of coking-produced organic carbon (OC) and elemental carbon (EC) remain unknown, causing considerable uncertainty in emission estimates. In this study, the emission factors of OC (EFOC) and EC (EFEC) of typical coking plants in Shanxi, China, were measured. The measured EFEC and EFOC from fugitive emissions (7.43 and 9.54 g/t) were significantly higher than those from flue gas (1.67 and 3.71 g/t). The technological conditions of coke production affect the emissions of OC and EC. For example, the total emissions from coke plants that use 3.2-m-high coke ovens were greater than those from plants that use 4.3- and 6-m-high ovens. The EFOC and EFEC for plants conducting stamp charging were considerably higher than those for plants using top charging. The stable carbon isotopes of total carbon (δ¹³CTC), OC (δ¹³COC), and EC (δ¹³CEC) for fly ash during coking were −23.74‰ to −24.17‰, −23.32‰ to −23.87‰, and −23.84‰ to −24.14‰, respectively, and no clear isotopic fractionation was found during coke production. Different EC/OC ratios from different emission pathways and the carbon isotope signature of coke production should be considered when investigating the sources of carbonaceous aerosols. The total estimated EC and OC emissions from coke production in China were 3.93 and 5.72 Gg in 2017, and Shanxi, Hebei, and Shaanxi made the largest contributions.

The installation rate of denitrification devices is accelerating in Chinese urban boilers. Previous studies on pulverized coal-fired boilers without denitrification devices showed that combustion products containing mainly oxidized mercury (Hg) preferably enriched lighter Hg isotopes than feed coals. However, the magnitude of this enrichment becomes less pronounced if denitrification devices are installed. The underlying Hg isotope fractionation mechanisms are still unclear. In this study, three types of urban boilers (two pulverized coal-fired boilers, one circulating fluidized bed boiler and one municipal waste incinerator boiler) all installed with denitrification devices were measured for Hg isotope compositions of their feed fuels and corresponding combustion products. We observed little mass independent fractionation but very significant mass dependent fractionation (MDF) between feed fuels and combustion products. The fly ash and desulfurization products both enriched heavier Hg isotopes than feed coals in three coal-fired boilers, and the enrichment of heavy Hg isotopes increased with sequential removal of combustion products in all boilers. Different from previously suggested kinetic MDF for gaseous Hg⁰(g)→Hgᴵᴵ(g) and gaseous Hgᴵᴵ(g)→particulate Hgᴵᴵ(p) in coal combustion flue gases, we propose an equilibrium MDF for Hg⁰(g)↔Hgᴵᴵ(g) followed by a kinetic MDF for Hgᴵᴵ(g)→Hgᴵᴵ(p). This equilibrium MDF most likely occurs during Hg⁰(g) oxidation in denitrification devices, which enriches heavy Hg isotopes in oxidized products (Hgᴵᴵ(g) and Hgᴵᴵ(p)) that are then sequestrated in fly ash and desulfurization products. The paradigm shift of MDF in boilers with denitrification devices was further verified by parallel Hg isotope measurement in urban atmosphere particulates. Our study clearly demonstrates that modern coal-fired boilers with denitrification devices have a quite different MDF compared to traditional boilers without denitrification devices. This has important implications for estimating isotope signatures of urban boiler Hg emissions, and for isotope tracing of anthropogenic Hg emissions.

Multi-layered engineered landfill consists of the bottom liner layer (mainly bentonite clay (B)) upon which the hazardous wastes are dumped. In current practice, sand (S) is mixed with bentonite to mitigate the adverse effects of using bentonite alone in the liner layer. Incorporation of waste and unutilized fly ash (FA) as an amendment material to B has been explored in terms of its hydro-mechanical properties, but not gauged its adsorption potential. Indian subcontinent primarily relies on the thermal power source, and FA dumps have already reached its full capacity. The objective of this study is to explore the adsorption characteristics of four B-FA composite mixes sourced within India, considering Pb²⁺ as a model contaminant. The effect of fly ash type, fly ash amendment rate and adsorbate concentration was explored in the current study and juxtaposed with B-S mixes, based on 960 batch adsorption tests. Both B-FA and B-S mixes reached equilibrium adsorption capacity within 65 min. At higher adsorbate concentrations (commonly observed in the liner), B-FA mixes exhibited superior adsorption capacity, mainly one mixed with Neyvelli fly ash (NFA). The effect of higher amendment rate had little impact on the adsorption capacity at different concentration, but gradually decreased the percentage removal of Pb²⁺. The B-S mix showed a drastic decrease in percentage removal at higher adsorbate concentration among all tested mixes. Systematic characterization including geotechnical properties, microstructure and chemical analysis was also done to interpret the obtained results. Both Freundlich and Langmuir models fitted the isotherm data well for all B-FA mixes. The maximum adsorption capacity from the isotherm was correlated to easily measurable Atterberg limits by two empirical relationships.

Apportioning sources of environmental pollutants is key to controlling pollution. In this study, the sources of heavy metals to 234 agricultural soils from the Jianghan Plain (JHP) (∼22454 km2) in central China were discriminated between using Cd and Pb isotope compositions and multivariate statistical analyses. Concentrations of some metals in JHP soils (0.48 ± 0.2, 48.2 ± 15.9, 0.12 ± 0.23, 48.8 ± 16.4, 36.5 ± 9.8, and 96.8 ± 42.2 mg kg−1 for Cd, Cu, Hg, Ni, Pb, and Zn, respectively) were higher than background concentrations in Chinese soil. The Cd isotope compositions for the JHP soils (δ114/110Cd values −0.76‰ to −0.25‰) were similar to Cd isotope compositions found for smelter dust and incinerator fly ash, indicating Cd was supplied to the JHP soils by ore smelting and/or refining processes. The Pb isotope compositions for the JHP soils (206Pb/207Pb 1.182–1.195 and 208Pb/206Pb 2.078–2.124) were between the Pb isotope compositions found for Chinese coal and natural sources, which a binary isotope mixing model indicated contributed 52% and 48%, respectively, of the Pb in JHP soils. Cluster analysis and positive matrix factorization indicated that the sources of heavy metals in JHP soils may consist of smelting and/or refining activities, coal combustion, agricultural activities, and natural sources (including Han River sediment and soil parent materials). The isotope fingerprints and multivariate statistical analyses together indicated that coal combustion and smelting and/or refining activities were the main anthropogenic sources of heavy metals polluting JHP soils.