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Passive sampling methodologies offer a series of advantages, providing time-averaged contamination levels in the field, separating the analyte from complex matrices, lowering the limits of quantification, and offering the possibilities of chemical fractionation and speciation. This review surveys the recent developments in passive samplers (PSs) tools such as diffusive gradients in thin films, polymer inclusion membranes, stabilized liquid membrane devices, “octopus” samplers, and active PSs. This article also discusses some challenges in the on-site utilization of these techniques and presents the latest on-site application of PSs to assess metals and metalloids in aquatic systems. Passive sampling is becoming a recognized practice, confirmed by numerous articles published in this field. Advances were made to increase the robustness, accuracy, and precision of the method, and collaborative studies were used for on-site validation. Chemical fractionation, speciation, and bioavailability of elements received special attention in recent years. This review provides a comprehensive update on the latest progress in passive sampling techniques. It brings together for the first time the newest developments of the most used PSs for metal and metalloid monitoring, speciation, and fractionation in aquatic systems. The potential contribution of passive sampling for metal and metalloid determination in water samples in achieving the analytical chemistry green and white analytical concept is also discussed.

The editorial discusses the importance of plant biomonitoring, bioremediation, and biomining in addressing environmental pollution. It highlights the use of hyperaccumulator plants for bioremediation and the challenges in developing ready-to-use technologies. The research also explores the role of different plant species in environmental recovery and the potential of lichens as biological indicators of air pollution. The study emphasizes the need for further investigations to enhance pollution monitoring and develop cost-effective bioremediation methods. [Extracted from the article]

Water treatment necessitates the sustainable use of natural resources. This paper focuses on the characterization of three oxidic lithological materials (OLMs) with the aim of utilizing them to prepare calcined adsorbent substrates for ionic adsorption. The three materials have pH levels of 7.66, 4.63, and 6.57, respectively, and organic matter contents less than 0.5%. All of the materials are sandy loam or loamy sand. Their electric conductivities (0.18, 0.07, and 0.23 dS/m) show low levels of salinity and solubility. Their CEC (13.40, 13.77, and 6.76 cmol(+)kg) values are low, similar to those of amphoteric oxides and kaolin clays. Their aluminum contents range from 7% up to 12%, their iron contents range from 3% up to 7%, their titanium contents range from 0.3% to 0.63%, and their manganese contents range from 0.007% up to 0.033%. The amphoteric oxides of these metals are responsible for their ionic adsorption reactions due to their variable charge surfaces. Their zirconium concentrations range from 100 to 600 mg/g, giving these materials the refractory properties necessary for the preparation of calcined adsorbent substrates. Our XRD analysis shows they share a common mineralogical composition, with quartz as the principal component, as well as albite, which leads to their thermal properties and mechanical resistance against abrasion. The TDA and IR spectra show the presence of kaolinite, which is lost during thermal treatments. The results show that the OLMs might have potential as raw materials to prepare calcined adsorbent substrates for further applications and as granular media in the sustainable treatment of both natural water and wastewater. [ABSTRACT FROM AUTHOR]

Interest in measuring major and trace elements in plants has increased in recent years because of growing concerns about the elements’ contribution to daily intakes or the health risks posed by ingesting vegetables contaminated by potentially toxic elements. The recent advances in using inductively coupled plasma atomic emission spectrometry (ICP-OES) to measure major and trace elements in plant samples are reviewed in the present work. The sample preparation before instrumental determination and the main advantages and limitations of ICP-OES are described. New trends in element extraction in liquid solutions using fewer toxic solvents and microextractions are observed in recently published literature. Even though ICP-OES is a well-established and routine technique, recent innovations to increase its performance have been found. Validated methods are needed to ensure the obtaining of reliable results. Much research has focused on assessing principal figures of merit, such as limits of detection, quantification, selectivity, working ranges, precision in terms of repeatability and reproducibility, and accuracy through spiked samples or certified reference materials analysis. According to the published literature, the ICP-OES technique, 50 years after the release of the first commercially available equipment, remains a powerful and highly recommended tool for element determination on a wide range of concentrations. [ABSTRACT FROM AUTHOR]

L-poly(lactic acid), poly(3-hydroxybutyrate), and poly-hydroxybutyrate-co-hydroxyvalerate are biodegradable polymers that can be obtained from renewable biomass sources. The aim of this study was to develop three types of environmentally friendly film biocomposites of altered microstructure by combining each of the above-mentioned polymers with cellulose nanocrystal fillers and further processing the resulting materials via space-confined solvent vapor annealing. Cellulose was previously obtained from renewable biomass and further converted to cellulose nanocrystals by hydrolysis with the lactic acid. The solutions of biodegradable polymers were spin-coated onto solid substrates before and after the addition of cellulose nanocrystals. The obtained thin film composites were further processed via space-confined solvent vapor annealing to eventually favor their crystallization and, thus, to alter the final microstructure. Indeed, atomic force microscopy studies have revealed that the presence of cellulose nanocrystals within a biodegradable polymer matrix promoted the formation of large crystalline structures exhibiting fractal-, spherulitic- or needle-like morphologies. [ABSTRACT FROM AUTHOR]

Precious metals such as palladium (Pd) have many applications, ranging from automotive catalysts to fine chemistry. Platinum group metals are, thus, in massive demand for industrial applications, even though they are relatively rare and belong to the list of critical materials for many countries. The result is an explosion of their price. The recovery of Pd from spent catalysts and, more generally, the development of a circular economy process around Pd, becomes essential for both economic and environmental reasons. To this aim, we propose a sustainable process based on the use of supercritical CO2 (i.e., a green solvent) operated in mild conditions of pressure and temperature (p = 25 MPa, T = 313 K). Note that the range of CO2 pressures commonly used for extraction is going from 15 to 100 MPa, while temperatures typically vary from 308 to 423 K. A pressure of 25 MPa and a temperature of 313 K can, therefore, be viewed as mild conditions. CO2-soluble copolymers bearing complexing groups, such as pyridine, triphenylphosphine, or acetylacetate, were added to the supercritical fluid to extract the Pd from the catalyst. Two supported catalysts were tested: a pristine aluminosilicate-supported catalyst (Cat D) and a spent alumina supported-catalyst (Cat A). An extraction conversion of up to more than 70% was achieved in the presence of the pyridine-containing copolymer. The recovery of the Pd from the polymer was possible after extraction, and the technological and economical assessment of the process was considered. [ABSTRACT FROM AUTHOR]

The study presents the current status of contamination with metals (Cu, Cr, Cd, Pb, Ni, Zn, As) and their anthropogenic or natural origin in the sediments of the Aries river basin, Romania, affected by mining activities. The results indicated an enrichment of metals in sediments. Different contamination levels were identified on the Aries river and its tributaries. According to sediment quality guidelines and contamination indices, sediments from the Aries river were found to be highly contaminated with Cd, Cu, As, considerably with Zn and moderately with Pb and Ni. The right-bank tributaries were found to be more contaminated than the left-bank affluents, where only a contamination with As of geogenic origin was identified. The Principal Component Analysis allowed to identify five latent factors (86 % total variability) reflecting the anthropogenic and natural origins of metals. Arsenic, Cd and partially Pb were found to have a common anthropogenic origin, different from that of Cu. The statistical approach indicated also the geogenic origin of Pb due to its association with Ca, K, Na, Sr. Chromium and Ni were attributed to natural source following their association with Mn, Fe, Al and Mg, respectively.

In order to evaluate the mobility of heavy metals in soil from Baia Mare mining region, the total, water and DTPA extractable metal contents were determined. The results showed that despite the high total metals contents and the high percentages of plant available metals only a low percent was water soluble, indicating a potential accumulation of metals in trophic chain and a potential risk for public health. Among the investigated metals, the plant available Pb and Cd species are the most severe contaminants. Significant correlations between total and DTPA extractable metals were found for Cu (r=0.510) and Pb (0.418), and also an affinity between total and water extractable metals were identified for Cu (0.366), Pb (0.502) and Zn (0.597).