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The leaching behavior of arsenic (As), lead (Pb), nickel (Ni), iron (Fe), and manganese (Mn) was investigated from subsurface core sediment of marine and nonmarine depositional environments in central Kanto Plain, Japan. A four-step sequential extraction technique was adopted to determine the chemical speciation, potential mobility, and bioavailability of metals under natural conditions in variable depositional environments. In addition, a correlation of these properties with pore water and total metal content was carried out. The concentration of As in pore water was found to be 2–3 times higher than the permissible limit (10 µg/L) for drinking water and leachate in fluvial, transitional, and marine environments. The trend of potential mobile fractions of As, Pb, and Ni showed Fe–Mn oxide bound > carbonate bound > ion exchangeable bound > water soluble in the fluvial environment. However, in the marine environment, it showed Fe–Mn oxide bound > water soluble > carbonate bound > ion exchangeable bound for As. The leaching of As in this fluvial environment is due to the organic matter-mediated, reductive dissolution of Fe–Mn oxide bound, where Mn is the scavenger. The amount of total content of As and sulfur (S) in transitional sediment reflects an elevated level of leachate in pore water, which is controlled by S reduction. However, the leaching of As in marine sediment is controlled by pH and organic matter content.

Electronic cigarettes (EC) deliver aerosol by heating fluid containing nicotine. Cartomizer EC combine the fluid chamber and heating element in a single unit. Because EC do not burn tobacco, they may be safer than conventional cigarettes. Their use is rapidly increasing worldwide with little prior testing of their aerosol. We tested the hypothesis that EC aerosol contains metals derived from various components in EC. Cartomizer contents and aerosols were analyzed using light and electron microscopy, cytotoxicity testing, x-ray microanalysis, particle counting, and inductively coupled plasma optical emission spectrometry. The filament, a nickel-chromium wire, was coupled to a thicker copper wire coated with silver. The silver coating was sometimes missing. Four tin solder joints attached the wires to each other and coupled the copper/silver wire to the air tube and mouthpiece. All cartomizers had evidence of use before packaging (burn spots on the fibers and electrophoretic movement of fluid in the fibers). Fibers in two cartomizers had green deposits that contained copper. Centrifugation of the fibers produced large pellets containing tin. Tin particles and tin whiskers were identified in cartridge fluid and outer fibers. Cartomizer fluid with tin particles was cytotoxic in assays using human pulmonary fibroblasts. The aerosol contained particles >1 µm comprised of tin, silver, iron, nickel, aluminum, and silicate and nanoparticles (<100 nm) of tin, chromium and nickel. The concentrations of nine of eleven elements in EC aerosol were higher than or equal to the corresponding concentrations in conventional cigarette smoke. Many of the elements identified in EC aerosol are known to cause respiratory distress and disease. The presence of metal and silicate particles in cartomizer aerosol demonstrates the need for improved quality control in EC design and manufacture and studies on how EC aerosol impacts the health of users and bystanders.

Heavy metal levels have steadily risen over the past century due to the presence of human activity and are hazardous to human health and the environment. Regarding the health of humans and the environment, palladium (Pd) is among the most hazardous and toxic heavy metals. It is listed as a priority contaminant by the Agency for Toxic Substances and Disease Registry (ATSDR). As a result, eliminating pollution and tracking changes in Pd contamination in the air are the top research priorities. This study will be conducted on trees grown in Düzce, the fifth dirtiest city on the European continent, to identify appropriate species that may be utilized for tracking and mitigating Pd pollution in the air. Samples from Cupressus arizonica, Pinus pinaster, Cedrus atlantica, Pseudotsuga menziesii, and Picea orientalis will all be analyzed as part of the study, and the variations in Pd content according to species, organ, and direction will be assessed. The goal is to ascertain which biomonitors are best suited for tracking and mitigating lead contamination in the atmosphere. The study consistently found Pd contents in woods with different directions that developed within the same period. However, when the species were compared, notable differences were detected between the Pd levels formed in different directions in the same period for each species and the wood formed in the same direction in other periods. This variation suggests that Pd transfer in wood is restricted in all tested species. Consequently, every species performs as a reliable biomonitor for tracking Pd contamination.

Electronic e-waste (e-waste) is a growing problem worldwide. In 2019, total global production reached 53.6 million tons, and is estimated to increase to 74.7 million tons by 2030. This rapid increase is largely fuelled by higher consumption rates of electrical and electronic goods, shorter life cycles and fewer repair options. E-waste is classed as a hazardous substance, and if not collected and recycled properly, can have adverse environmental impacts. The recoverable material in e-waste represents significant economic value, with the total value of e-waste generated in 2019 estimated to be US $57 billion. Despite the inherent value of this waste, only 17.4% of e-waste was recycled globally in 2019, which highlights the need to establish proper recycling processes at a regional level. This review provides an overview of global e-waste production and current technologies for recycling e-waste and recovery of valuable material such as glass, plastic and metals. The paper also discusses the barriers and enablers influencing e-waste recycling with a specific focus on Oceania.

With industrialization, great amounts of trace elements and heavy metals have been excavated and released onto the surface of the earth and dissipated into the environments. Rapid screening technology for detecting major and trace elements as well as heavy metals in variety of environmental samples has been most desired. The objectives of this study were to determine the detection limits, accuracy, repeatability, and efficiency of an X-ray fluorescence spectrometer (Niton XRF analyzer) in comparison to the traditional analytical methods, inductively coupled plasma optical emission spectrometer (ICP-OES) in screening of major and trace elements of environmental samples including estuary soils and sediments, contaminated soils, and biological samples. XRF is a fast and non-destructive method for measuring the total concentration of multi-elements simultaneously. Contrary to ICP-OES, XRF analyzer is characterized by the limited preparation required for solid samples, non-destructive analysis, increased total speed and high throughout, decreased production of hazardous waste, and low running costs as well as multi-elemental determination and portability in the fields. The current comparative study demonstrates that XRF is a good rapid, non-destructive screening method for contaminated soils, sediments, and biological samples containing high concentrations of major and trace elements. Unfortunately, XRF does not have sensitive detection limits for most trace elements as ICP-OES, but it may serve as a rapid screening tool for locating hot spots in uncontaminated field soils and sediments, such as in the US Department of Energy’s Oak Ridge site.

Emerging and low-carbon technologies and innovations are driving a need for domestic sources, sustainable use, and availability of critical minerals (CMs)—those vital to the national and economic security of the United States. Understanding the known and potential health effects of exposures to such mineral commodities can inform prudent and environmentally responsible handling and harvesting. We review the occurrence, use, predominant exposure pathways, and adverse outcome pathways (AOP) for human and fish receptors of those CMs that are nutritionally essential trace metals (specifically, cobalt, chromium, manganese, nickel, and zinc), as well as the rare earth elements. Biological responses to some elements having comparable biogeochemistry can sometimes be similar. Candidate quantifiable biomarkers for assessing potential AOP are conveyed.

BackgroundLittered cigarette butts represent potential point sources for environmental contamination. In areas with substantial amounts of cigarette litter, environmental hazards may arise as chemical components are leached from the filters and smoked tobacco.ObjectiveThe three main aims of this study were: (1) to quantify the amount of Al, Ba, Cd, Cr, Cu, Fe, Pb, Mn, Ni, Sr, Ti and Zn leached from cigarette butts, (2) to determine the relationship between the pH of the aqueous soaking solution and metal concentration leached and (3) to determine the relationship between the period of soaking in aqueous solution and metal concentration leached.MethodsSmoked cigarette butts and unsmoked cigarettes were added to phials containing aqueous solutions of pH 4.00, 5.00 and 6.00 (±0.05). The metal concentration of the resultant leachates was measured via inductively coupled plasma optical emission spectroscopy (ICP-OES) 1 day, 7 days and 34 days after sample addition.ResultsAll metals were detected in leachates 1 day after sample addition (with the exception of Cd) and were released at varying rates. No clear relationship between pH within the range typical of precipitation and metal concentration leached was observed.ConclusionsBased on the gradual release of multiple metals over the full 34-day study period, cigarette litter was found to be a point source for metal contamination. The apparent rapid leaching of other metals may increase the risk of acute harm to local organisms.

Wine is one of the most popular alcoholic beverages. Therefore, the control of the elemental composition is necessary throughout the entire production process from the grapes to the final product. The content of some elements in wine is very important from the organoleptic and nutritional points of view. Nowadays, wine studies have also been undertaken in order to perform wine categorization and/or to verify the authenticity of products. The main objective of this research was to evaluate the influence of the chosen factors (type of wine, producer, origin) on the levels of 28 elements in 180 wine samples. The concentration of studied elements was determined by ICP-MS (Ag, B, Ba, Be, Bi, Cd, Co, Cr, Cu, Li, Mn, Mo, Ni, Pb, Rb, Sb, Sn, Sr, Te, Tl, U, Zn), ICP-OES (Ca, Fe, K, Mg, Ti), and CVAAS (Hg) techniques in 79 red, 75 white, and 26 rose wine samples. In general, red wines contained higher values of mean and median of B, Ba, Cr, Cu, Mn, Sr and Zn in contrast to other wine types (white and rose). In white wines (when compared to red and rose wines) higher levels of elements such as Ag, Be, Bi, Cd, Co, Li, K and Ti were determined. In contrast, rose wines were characterized by a higher concentration of Fe and U. The study also revealed that in the case of 18 samples, the maximum levels of some metals (Cd—8 samples, Pb—9 samples, Cu—1 sample) were slightly exceeded according to the OIV standards, while for Zn and Ti in any wine sample the measured concentrations of these metals were above the permissible levels. Thus, it can be stated that the studied wines contained, in general, lower levels of heavy metals, suggesting that they should have no effect on the safety of consumption. The results also showed higher pH level for red wines as a consequence of the second fermentation process which is typically carried out for this type of wine (malolactic fermentation). The highest median value of pH was reported for Merlot-based wines, while the lowest was for Riesling. It is assumed that dry Riesling has a higher content of tartaric and malic acid than dry Chardonnay grown in the same climate. From all of the studied countries, wines from Poland seemed to present one of the most characteristic elemental fingerprints since for many elements relatively low levels were recorded. Moreover, this study revealed that also wine samples from USA and Australia can be potentially discriminated from the rest of studied wines. For USA the most characteristic metal for positive identification of the country of origin seems to be uranium, whereases for Australia – strontium and manganese. Based on the highly reduced set of samples, it was not possible to differentiate the studied wine products according to the grape variety other than Syrah, and partially Chardonnay. Since all the Syrah-based samples originated from the same country (Australia) thus, the observed grouping should be more related with the country of origin than the grape variety.

A nationwide investigation was carried out to evaluate the geochemical characteristics and environmental impacts of red mud and leachates from the major alumina plants in China. The chemical and mineralogical compositions of red mud were investigated, and major, minor, and trace elements in the leachates were analyzed. The mineral and chemical compositions of red mud vary over refining processes (i.e., Bayer, sintering, and combined methods) and parental bauxites. The main minerals in the red mud are quartz, calcite, dolomite, hematite, hibschite, sodalite, anhydrite, cancrinite, and gibbsite. The major chemical compositions of red mud are Al, Fe, Si, Ca, Ti, and hydroxides. The associated red mud leachate is hyperalkaline (pH > 12), which can be toxic to aquatic life. The concentrations of Al, Cl−, F−, Na, NO32−, and SO42− in the leachate exceed the recommended groundwater quality standard of China by up to 6637 times. These ions are likely to increase the salinization of the soil and groundwater. The minor elements in red mud leachate include As, B, Ba, Cr, Cu, Fe, Ni, Mn, Mo, Ti, V, and Zn, and the trace elements in red mud leachate include Ag, Be, Cd, Co, Hg, Li, Pb, Sb, Se, Sr, and Tl. Some of these elements have the concentration up to 272 times higher than those of the groundwater quality standard and are toxic to the environment and human health. Therefore, scientific guidance is needed for red mud management, especially for the design of the containment system of the facilities.

With the development of industry, sustainable use of natural resources has become a worldwide hot topic. Heavy metal–containing sludge (HMS) is a hazardous waste after wastewater treatment. At present, HMS is still treated by landfill or landfill after incineration. Considering the components, HMS usually contains various heavy metals and organic compounds, which is potentially used as a raw resource for catalyst production. This review thus concludes recent reports and developments in this field. First, basic technologies are summarized as component regulation, precursor formation, and structure transformations. Second, prepared materials are applied in various catalytic fields, such as gas purification, photocatalysis, electrocatalysis, and Fenton catalysis. During these processes, key factors are multi-metallic components, metal doping, temperature, and pH. They not only influence the formation of HMS-derived catalyst but also the catalytic activity. Furthermore, catalytic activities of HMS-derived catalysts are compared with those synthesized by pure reagents. An assessment and accounting are also supplied if raw resources are substituted by HMS. Finally, in order to apply HMS in a real application, more works must be devoted to the influence of trace metal doping on catalytic activities and stabilities. Besides, more pilot experiments are urgently necessary.