Distribution of Platinum and Palladium between Dissolved, Nanoparticulate, and Microparticulate Fractions of Road Dust.

Ageing processes of vehicle catalytic converters inevitably lead to the release of Pt and Pd into the environment, road dust being the main sink. Though Pt and Pd are contained in catalytic converters in nanoparticulate metallic form, under environmental conditions, they can be transformed into toxic dissolved species. In the present work, the distribution of Pt and Pd between dissolved, nanoparticulate, and microparticulate fractions of Moscow road dust is assessed. The total concentrations of Pt and Pd in dust vary in the ranges 9-142 ng (mean 35) and 155-456 (mean 235) ng g-1, respectively. The nanoparticulate and dissolved species of Pt and Pd in dust were studied using single particle inductively coupled plasma mass spectrometry. The median sizes of nanoparticulate Pt and Pd were 7 and 13 nm, respectively. The nanoparticulate fraction of Pt and Pd in Moscow dust is only about 1.6-1.8%. The average contents of dissolved fraction of Pt and Pd are 10.4% and 4.1%, respectively. The major fractions of Pt and Pd (88-94%) in road dust are associated with microparticles. Although the microparticulate fractions of Pt and Pd are relatively stable, they may become dissolved under changing environmental conditions and, hence, transformed into toxic species.

Natural silicate nanoparticles: separation, characterization, and assessment of stability and perspectives of their use as reference nanomaterials.

Natural nanomaterials, which play a very important role in environmental processes, are so far poorly studied. Firstly, the separation of nanoparticles from the bulk sample is a challenge. Secondly, the absence of reference natural nanomaterials makes it impossible to compare the results obtained by different researchers and develop a unified methodology for the separation and characterization of natural nanomaterials. Therefore, the development of reference natural nanomaterials is an urgent need of the environmental analytical chemistry. In this work, mineral nanoparticles (kaolinite, montmorillonite, muscovite, and quartz) have been studied as potential reference natural nanomaterials. A set of analytical methods including coiled-tube field-flow fractionation, scanning electron microscopy, dynamic light scattering, laser diffraction, inductively coupled plasma atomic emission, and mass spectrometry are applied to the separation and characterization of nanoparticles. It has been shown by laser diffraction that 93-98% of separated mineral nanoparticles are in the size range from about 40 to 300 nm, while 2-7% have size up to 830 nm. The size range of particles is confirmed by electron microscopy. Major (Al, Na, K, Ca, Fe), trace (Ti, Co, Cu, Zn, Tl, Pb, Bi, etc.), and rare earth elements have been determined in the suspensions of kaolinite, montmorillonite, and muscovite nanoparticles. Based on Al content, the concentration of mineral nanoparticles in suspensions is estimated. Agglomeration stability (consistency of size distribution) of nanoparticles at pH 6-8 is assessed. It has been shown that muscovite nanoparticles are stable at pH 7-8, whereas montmorillonite nanoparticles are stable only at pH 8 for at least 4 weeks. A noticeable agglomeration of kaolinite nanoparticles is observed at pH 6-8. Due to the low concentration of quartz nanoparticles, their characterization and stability assessment are hindered. The challenges of the development of reference natural nanomaterials are discussed.

Separation of nanoparticles from polydisperse environmental samples: comparative study of filtration, sedimentation, and coiled tube field-flow fractionation.

Nanoparticles (NPs) in the environment have a potential risk for human health and the ecosystem due to their ubiquity, specific characteristics, and properties (extreme mobility in the environment, abilities to accumulate of toxic elements and penetrate into living organisms). There is still a gap in studies on the chemical composition of natural NPs. The main reason is the difficulty to recover NPs, which may represent only one-thousandth or less of the bulk environmental sample, for further dimensional and quantitative characterization. In the present study, a methodology for the recovery of the nanoparticle fraction from polydisperse environmental samples was developed taking as example volcanic ashes from different regions of the world. For the first time, three separation methods, namely, filtration through a 0.45-µm membrane, sedimentation, and coiled tube field-flow fractionation (CTFFF), were comparatively studied. The separated fractions were characterized by laser diffraction and scanning electron microscopy and then analyzed by inductively coupled plasma atomic emission and mass spectrometry. It has been shown that all three methods provide the separation of NPs less than 400 nm from the bulk material. However, the fraction separated by sedimentation also contained a population (5% in mass) of submicron particles (~ 400-900 nm). The filtration resulted in low recovery of NPs. The determination of most trace elements was then impossible; the concentration of elements was under the limit of detection of the analytical instrument. The sedimentation and CTFFF made it possible to determine quantifiable concentrations for both major and trace elements in separated fractions. However, the sedimentation took 48 h while CTFFF enabled the fractionation time to be decreased down to 2 h. Hence, CTFFF looked to be the most promising method for the separation of NPs followed by their quantitative elemental analysis.

Assessment of elemental composition and properties of copper smelter-affected dust and its nano- and micron size fractions.

A comprehensive approach has been developed to the assessment of composition and properties of atmospherically deposited dust in the area affected by a copper smelter. The approach is based on the analysis of initial dust samples, dynamic leaching of water soluble fractions in a rotating coiled column (RCC) followed by the determination of recovered elements and characterization of size, morphology and elemental composition of nano-, submicron, and micron par ticles of dust separated using field-flow fractionation in a RCC. Three separated size fractions of dust (<0.2, 0.2-2, and >2 µm) were characterized by static light scattering and scanning electron microscopy, whereupon the fractions were analyzed by ICP-AES and ICP-MS (after digestion). It has been evaluated that toxic elements, which are characteristics for copper smelter emissions (As, Cu, Zn), are accumulated in fraction >2 µm. At the same time, up to 2.4, 3.1, 8.2, 6.7 g/kg of As, Cu, Zn, Pb, correspondently, were found in nanoparticles (<0.2 µm). It has been also shown that some trace elements (Sn, Sb, Ag, Bi, and Tl) are accumulated in fraction <0.2, and their content in this fraction may be one order of magnitude higher than that in the fraction >2 µm, or the bulk sample. It may be assumed that Sn, Sb, Ag, Bi, Tl compounds are adsorbed onto the finest dust particles as compared to As, Cu, Zn compounds, which are directly emitted from the copper smelter as microparticles.

A contribution of nanoscale particles of road-deposited sediments to the pollution of urban runoff by heavy metals.

Road-deposited sediments (RDS) present a sink for traffic-related pollutants including heavy metals (HMs). HMs associated with RDS particles enter the urban aquatic environment during rainfall events and have adverse effects for biota. RDS nanoscale particles (NSPs) require special consideration due to their specific properties, extremely high mobility in the environment, and ability to penetrate into living organisms. In the present work, the contribution of NSPs of RDS to the pollution of urban runoff by HMs has been evaluated for the first time. It has been shown that bulk RDS samples are polluted by HMs as compared to background urban soils (geo-accumulation indexes of Cu and Zn may attain 2-3). Meanwhile, NSPs of RDS are enriched by HMs as compared to bulk samples; concentration factor for Ni, Cu, Zn, Cd, Sn, and Pb in NSPs being varied from 2 to 10. The water-soluble fractions of RDS samples were also analyzed. Results have shown that the content of water-soluble HMs in RDS is insignificant and rarely exceeds 0.5% of the total contents of HMs in the bulk samples; the highest contents are identified for Cu and Pb. It should be noted that the water-soluble fraction is nearly free from Zn and this element is almost entirely present as particulate matter (NSPs). In general, the overall contribution of NSPs and water-soluble fraction of HMs to the pollution of urban runoff is comparable.

Nanoparticles of volcanic ash as a carrier for toxic elements on the global scale.

At present, there is concern about engineered nanoparticles in the environment, whereas natural nanoparticles (NPs) and their impact are often neglected. In our paper, we demonstrate the important role of nanoparticles of volcanic ash in transport of toxic elements on a global scale. A single volcanic eruption can eject millions of tons of ash. NPs of volcanic ash reach the upper troposphere and the stratosphere and may "travel" around the world for years affecting human health, environment, and even climate. So far, there is a gap in exposure assessment of volcanic ash NPs since their chemical composition remains largely unknown. Here we show for the first time that volcanic ash NPs can serve as an important carrier for potentially toxic elements. The concentrations of Ni, Zn, Cd, Ag, Sn, Se, Te, Hg, Tl, Pb, Bi in volcanic ash NPs (<100 nm) were found to be 10-500 times higher than total contents of these elements in bulk samples. This is valid for volcanoes from different regions of the world (Kamchatka, Far East of Russia and Andes, Chile). The work opens a new door into studies on biogeochemical impact of volcanic ash.

Combination of ICP-MS, capillary electrophoresis, and their hyphenation for probing Ru(III) metallodrug-DNA interactions.

Determination of the DNA-binding reactivity and affinity is an important part of a successful program for the selection of metallodrug candidates. For such assaying, a range of complementary analytical techniques was proposed and tested here using one of few anticancer metal-based drugs that are currently in clinical trials, indazolium trans-[tetrachloridobis(1H-indazole)ruthenate(III), and a DNA oligonucleotide. A high reactivity of the Ru drug was confirmed in affinity capillary electrophoresis (CE) mode, where adduct formation takes place in situ (i.e., in the capillary filled with an oligonucleotide-containing electrolyte). To further characterize the binding kinetics, a drug-oligonucleotide mixture was incubated for a different period of time, followed by ultrafiltration separation into two different in molecular weight fractions (>3 and <3 kDa). The time-dependent distribution profiles of the Ru drug were then assessed by CE-inductively coupled plasma mass spectrometry (ICP-MS), revealing that at least two DNA adducts exist at equilibrium conditions. Using standalone ICP-MS, dominant equilibrium amount of the bound ruthenium was found to occur in a fraction of 5-10 kDa, which includes the oligonucleotide (ca. 6 kDa). Importantly, in all three assays, the drug was used for the first time in in-vitro studies, not in the intact form but as its active species released from the transferrin adduct at simulated cancer cytosolic conditions. This circumstance makes the established analytical platform promising to provide a detailed view on metallodrug targeting, including other possible biomolecules and ex vivo samples.

Assessment of elemental composition and properties of copper smelter-affected dust and its nano- and micron size fractions.

A comprehensive approach has been developed to the assessment of composition and properties of atmospherically deposited dust in the area affected by a copper smelter. The approach is based on the analysis of initial dust samples, dynamic leaching of water soluble fractions in a rotating coiled column (RCC) followed by the determination of recovered elements and characterization of size, morphology and elemental composition of nano-, submicron, and micron particles of dust separated using field-flow fractionation in a RCC. Three separated size fractions of dust (<0.2, 0.2-2, and >2 µm) were characterized by static light scattering and scanning electron microscopy, whereupon the fractions were analyzed by ICP-AES and ICP-MS (after digestion). It has been evaluated that toxic elements, which are characteristics for copper smelter emissions (As, Cu, Zn), are accumulated in fraction >2 µm. At the same time, up to 2.4, 3.1, 8.2, 6.7 g/kg of As, Cu, Zn, Pb, correspondently, were found in nanoparticles (<0.2 µm). It has been also shown that some trace elements (Sn, Sb, Ag, Bi, and Tl) are accumulated in fraction <0.2, and their content in this fraction may be one order of magnitude higher than that in the fraction >2 µm, or the bulk sample. It may be assumed that Sn, Sb, Ag, Bi, Tl compounds are adsorbed onto the finest dust particles as compared to As, Cu, Zn compounds, which are directly emitted from the copper smelter as microparticles.

Continuous-flow leaching in a rotating coiled column for studies on the mobility of toxic elements in dust samples collected near a metallurgic plant.

Continuous-flow (dynamic) leaching in a rotating coiled column has been applied to studies on the mobility of Zn, Cd, Cu, Pb, Ni, Sb, As, S, and other potentially toxic elements in atmospherically deposited dust samples collected near a large copper smelter (Chelyabinsk region, Russia). Water and simulated "acid rain" (pH 4) were used as eluents. The technique enables not only the fast and efficient leaching of elements but as well time-resolved studies on the mobilization of heavy metals, sulphur, and arsenic in environmentally relevant forms to be made. It is shown that up to 1.5, 4.1, 1.9, 11.1, and 46.1% of Pb, As, Cu, Zn, and S, correspondingly, can be easily mobilized by water. Taking into consideration that the total concentrations of these elements in the samples under investigation are surprisingly high and vary in the range from 2.7 g/kg (for arsenic) to 15.5 g/kg (for sulphur), the environmental impact of the dust may be dramatic. The simulated acid rain results in somewhat higher recoveries of elements, except Cu and Pb. The proposed approach and the data obtained can very useful for the risk assessment related to the mobility of potentially toxic elements and their inclusion in the biogeochemical cycle.

Characterization of size, morphology and elemental composition of nano-, submicron, and micron particles of street dust separated using field-flow fractionation in a rotating coiled column.

For the first time, nano- and submicron particles of street dust have been separated, weighted, and analyzed. A novel technique, sedimentation field-flow fractionation in a rotating coiled column, was applied to the fractionation of dust samples with water being used as a carrier fluid. The size and morphology of particles in the separated fractions were characterized by electronic microscopy before digestion and the determination of the concentration of elements by ICP-AES and ICP-MS. The elements that may be of anthropogenic origin (Zn, Cr, Ni, Cu, Cd, Sn, Pb) were found to concentrate mainly in <0.3 and 0.3-1 µm fractions. It has been shown that the concentrations of Cr, Ni, Zn in the finest fraction (<0.3 µm) of street dust can be one order of magnitude higher than the concentrations of elements in bulk sample and coarse fractions. For example, the concentrations of Ni in <0.3, 0.3-1, 1-10, and 10-100 µm fractions were 297 ± 46, 130 ± 21, 36 ± 10, and 21 ± 4 mg/kg, correspondingly. Though the finest particles present only about 0.1 mass% of the sample they are of special concern due to their increased mobility and ability to penetrate into the deepest alveolar area of the lungs. For rare earth elements (La, Ce, Pr, Nd, Sm) that are evidently of natural source and may be found in soil minerals, in contrary, higher concentrations were observed in large particles (10-100 µm). Sc was an exception that needs further studies. The proposed approach to the fractionation and analysis of nano-, submicron, and micron particles can be a powerful tool for risk assessment related to toxic elements in dust, ash, and other particulate environmental samples.