Evaluation of health impacts arising from inhalation of pollutant particles <10 μm (PM10) is an active research area. However, lack of exposure data at high spatial resolution impedes identification of causal associations between exposure and illness. Biomagnetic monitoring of PM10 deposited on tree leaves may provide a means of obtaining exposure data at high spatial resolution. To calculate ambient PM10 concentrations from leaf magnetic values, the relationship between the magnetic signal and total PM10 mass must be quantified, and the exposure time (via magnetic deposition velocity (MVd) calculations) known. Birches display higher MVd (∼5 cm−1) than lime trees (∼2 cm−1). Leaf saturation remanence values reached ‘equilibrium’ with ambient PM10 concentrations after ∼6 ‘dry’ days (<3 mm/day rainfall). Other co-located species displayed within-species consistency in MVd; robust inter-calibration can thus be achieved, enabling magnetic PM10 biomonitoring at unprecedented spatial resolution.

The effectiveness and mechanism of nano-hydroxyapatite particles (nHAp) in immobilizing Pb and Cd from aqueous solutions and contaminated sediment were investigated. The maximum sorption amount (Qmax) of Pb and Cd in aqueous solution was 1.17 and 0.57 mmol/g. The X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) surface and depth analysis indicated that dissolution-precipitation is the primary immobilization mechanism for Pb, while surface complexation and intraparticle diffusion account for Cd sequestration. Different amounts of nHAp (0–10% nHAp/dry weight) were added to the contaminated sediment. Sequential extraction showed that nHAp could effectively reduce the exchangeable fraction of Pb and Cd in the sediment and significantly reduce the concentration in porewater. The results in this study showed that nHAp can immobilize Pb and Cd in sediment effectively. Nano-hydroxyapatite shows potential and advantages to immobilize lead and cadmium in aqueous solution and sediment.

Trace elements, especially those associated with fine particles in airborne particulate matter (PM), may play an important role in PM adverse health effect. The aim of this paper is to characterize elements in a wide particle size range from nano (57-100 nm) to fine (100-1,000 nm) and to coarse (1,000-10,000 nm) fractions of two urban PM samples collected in Ottawa. Size-selective particle sampling was performed using a micro-orifice uniform deposit impactor, and element concentrations were determined in each different size fraction by inductively coupled plasma-mass spectroscopy. A general trend of increasing element concentration with decreasing aerodynamic diameter was observed for elements V, Mn, Ni, Cu, Zn, Se, and Cd, indicating they were predominately concentrated in the nanoparticle size range. Other elements including Fe, Sr, Mo, Sn, Sb, Ba, and Pb were predominately concentrated in the fine-size range. Increased concentration of elements in the nano and fine particle size range is significant due to their ability to penetrate into the deepest alveolar area of the lungs. This was confirmed by the calculation of median concentration diameters, which were less than 800 nm for most of the investigated elements. Particle size distribution and element correlation analysis suggest that the elements concentrated in the nano- and fine-size fractions originated mainly from vehicular combustion and emission. Long-range airborne transport and soil or road dust resuspension may also contribute. Particle size had an important effect on element bioaccessibility for the studied urban PM samples showing a general trend of increasing element bioaccessibility with decreasing particle size. These results emphasize the importance of acquiring information on nano and/or fine PM-bound elements and their bioaccessibilities for accurate element and PM exposure assessment.

Present research has delineated the biosorption potential of three different nonliving biomasses namely eucalyptus bark saw dust, mango bark saw dust, and pineapple fruit peel with respect to Zn (II) ion removal from liquid phase through batch experiments. The efficacy of Zn (II) ion biosorption onto surface of biosorbents was judged and correlated with biosorbent particle size, surface chemistry, and surface texture. Maximum metal ion uptake capacity, percentage removal, and minimum equilibrium concentration as 1.688 mg/g, 84.4%, and 1.56 mg/l, respectively, was obtained using eucalyptus bark saw dust mediated biosorption followed by mango bark saw dust as 1.028 mg/g, 51.4%, and 4.867 mg/l and pineapple fruit peel as 0.45 mg/g, 22.9%, and 7.71 mg/l, respectively, at a particle size of 0.5 mm. Additionally, present investigation also proved that biosorption efficiency and metal ion interaction with adsorbent surface also depends upon presence of functional groups involved in metal ion adsorption and surface porosity.

Cattle manure vermicompost has been used for the adsorption of Al(III) and Fe(II) from both synthetic solution and kaolin industry wastewater. The optimum conditions for Al(III) and Fe(II) adsorption at pH 2 (natural pH of the wastewater) were particle size of ≤250 µm, 1 g/10 mL adsorbent dose, contact time of 4 h, and temperature of 25°C. Langmuir and Freundlich adsorption isotherms fitted reasonably well in the experimental data, and their constants were evaluated, with R ² values from 0.90 to 0.98. In synthetic solution, the maximum adsorption capacity of the vermicompost for Al(III) was 8.35 mg g⁻¹ and for Fe(II) was 16.98 mg g⁻¹ at 25°C when the vermicompost dose was 1 g 10 mL⁻¹, and the initial adjusted pH was 2. The batch adsorption studies of Al(III) and Fe(II) on vermicompost using kaolin wastewater have shown that the maximum adsorption capacities were 1.10 and 4.30 mg g⁻¹, respectively, at pH 2. The thermodynamic parameter, the Gibbs free energy, was calculated for each system, and the negative values obtained confirm that the adsorption processes were spontaneous.

Background, aim, and scope Nanomaterials have been used increasingly in industrial production and daily life, but their human exposure may cause health risks. The interactions of nanomaterial with functional biomolecules are often applied as a precondition for its cytotoxicity and organ toxicity where various proteins have been investigated in the past years. In the present study, nano-TiO₂ was selected as the representative of nanomaterials and lysozyme as a representative for enzymes. By investigating their interaction by various instrumentations, the objective is to identify the action sites and types, estimate the effect on the enzyme structure and activity, and reveal the toxicity mechanism of nanomaterial. Materials and methods Laboratory-scale experiments were carried out to investigate the interactions of nano-TiO₂ with lysozyme. The interaction of nano-TiO₂ particles with lysozyme has been studied in the analogous physiological media in detail by UV spectrometry, fluorophotometry, circular dichroism (CD), scanning electron microscope, ζ-potential, and laser particle size. Results The interaction accorded with the Langmuir isothermal adsorption and the saturation number of lysozyme is determined to be 580 per nano-TiO₂ particle (60 nm of size) with 4.7 × 10⁶ M⁻¹ of the stability constant in the physiological media. The acidity and ion strength of the media obviously affected the binding of lysozyme. The warping and deformation of the lysozyme bridging were demonstrated by the conversion of its spatial structure from α-helix into a β-sheet, measured by CD. In the presence of nano-TiO₂, the bacteriolysis activity of lysozyme was subjected to an obvious inhibition. Discussion The two-step binding model of lysozyme was proposed, in which lysozyme was adsorbed on nano-TiO₂ particle surface by electrostatic interaction and then the hydrogen bond (N-H···O and O-H···O) formed between nano-TiO₂ particle and polar side groups of lysozyme. The adsorption of lysozyme obeyed the Langmuir isothermal model. The binding of lysozyme is dependent on the acidity and ion strength of the media. The bigger TiO₂ aggregate was formed in the presence of lysozyme where lysozyme may bridge between nano-TiO₂ particles. The coexistence of nano-TiO₂ particles resulted in the transition of lysozyme conformation from an α-helix into a β-sheet and a substantial inactivation of lysozyme. The β-sheet can induce the formation of amyloid fibrils, a process which plays a major role in pathology. Conclusions Lysozyme was adsorbed on the nano-TiO₂ particle surface via electrostatic attraction and hydrogen bonds, and they also bridged among global nano-TiO₂ particles to form the colloidal particles. As a reasonable deduction of this study, nano-TiO₂ might have some toxic impacts on biomolecules. Our data suggest that careful attention be paid to the interaction of protein and nanomaterials. This could contribute to nanomaterial toxicity assessment. Recommendations and perspectives Our results strongly suggest that nano-TiO₂ has an obvious impact on biomolecules. Our data suggest that more attention should be paid to the potential toxicity of nano-TiO₂ on biomolecules. Further research into the toxicity of nanosized particles needs to be carried out prior to their cell toxicity and tissue toxicity. These investigations might serve as the basis for determining the toxicity and application of nanomaterials.

PURPOSES AND AIMS: Economically efficient methods for removing arsenic from the drinking water supply are urgently needed in many parts of the world. Iron oxides are known to have a strong affinity for arsenic in water. However, they are commonly present in the forms of fine powder or floc, which limits their utility in water treatment. In this study, a novel granular adsorbent, iron-oxide-coated diatomite (IOCD), was developed and examined for its adsorption of arsenic from water. MATERIALS AND METHODS: An industrial-grade diatomite was used as the iron oxide support. The diatomite was first acidified and dried and then coated with iron oxide up to five times. The prepared IOCD samples were characterized for their morphology, composition, elemental content, and crystal properties by various instruments. Experiments of equilibrium and kinetic adsorption of As(V) on IOCD were conducted using 0.1- and 2-L polyethylene bottles, respectively, at different pH and temperatures. RESULTS: Iron oxide (α-Fe₂O₃ hematite) coated onto diatomite greatly improves (by about 30 times) the adsorption of As(V) from water by IOCD as compared to using raw diatomite. This improvement was attributed to increases in both surface affinity and surface area of the IOCD. The surface area of IOCD increased to an optimal value. However, as the IOCD surface area (93 m²/g) was only 45% higher than that of raw diatomite (51 m²/g), the enhanced As(V) adsorption resulted primarily from the enhanced association of negatively charged As(V) ions with the partial positive surface charge of the iron oxide. The As(V) adsorption decreased when the solution pH was increased from 3.5 to 9.5, as expected from the partial charge interaction between As(V) and IOCD. The adsorption data at pH 5.5 and 7.5 could be well fitted to the Freundlich equation. A moderately high exothermic heat was observed for the As(V) adsorption, with the calculated molar isosteric heat ranging from −4 to −9 kcal/mol. The observed heats fall between those for physical adsorption and chemisorption and are indicative of the formation of a series of ion-pair complexes of As(V) ions with iron oxide surface groups. CONCLUSIONS: This study demonstrated that the granular IOCD was successfully developed and employed to remove the As(V) in aqueous solution. The Freundlich isotherm well fitted the equilibrium adsorption data of As(V) onto IOCD, and both the pseudo-second-order model and the pore diffusion model simulated well the adsorption kinetics. Compared to other iron-oxide-based adsorbents reported in the literatures, the adsorption capacity of IOCD is relatively high and its kinetics is fast.

Background, aim, and scope Transport of bacteria through natural porous media is an issue of increasing concern arising in several very important environmental processes. These include the percolation of bacteria from fecal waste to drinking water reservoirs, thus leading to a risk for human health, or the bioremediation of contaminated soils in which the bacteria are expected to travel long distances underground in order to reach contaminated areas and degrade chemicals originating from accidental spills. An understanding of bacterial retention and transport mechanisms in porous media would be of great help in the development of models able to predict the distance covered by bacterial suspensions in these situations. Materials and methods Experiments were carried out preparing columns filled of soil and sand, introducing bacteria culture (Escherichia coli, Pseudomona putida, and Listeria innocua) solutions by the top of the column. Breakthrough curves were obtained to see the transport of the bacteria in the column. Results The transport of different bacteria in the two soils aimed at establishing the relative importance of straining in different conditions. This has enabled us to obtain certain parameters, such as the sticking coefficients derived from the filtration theory or bacterial recoveries after multi-step elution, which aid our understanding of how bacteria are retained by mechanisms different to those usually included in the physico-chemical filtration theory. Discussion Several indicators may be used to determine the degree of relevance of straining as a mechanism acting during bacterial transport through porous media. Usually, in natural media, neither straining nor physico-chemical filtration is the sole mechanism contributing to bacterial retention. The retention of bacteria by straining mechanisms can be assessed by means of elution profiles under varying conditions. The inversion of flow in our experiments gave rise to secondary elution peaks, probably originating from bacteria retained in narrow pores Conclusions According to experimental observations, straining was shown to contribute highly to bacterial retention in all the soils tested, in particular in the soils with a broader grain size distribution and more irregular shape. In both media, an increase in ionic strength did not lead to significant differences in bacterial retention, possibly due to the lack of relevance of ionic repulsion as a barrier to physico-chemical attachment of particles Recommendation and perspectives The study of bacteria transport in natural soil is an important step in the development of decontamination processes. The importance of the straining in the transport process has been revealed in the work carried out in this paper.