Metal ion release from fine particulate matter sampled in the Po Valley to an aqueous solution mimicking fog water: Kinetics and solubility

Metals are among the key aerosol components exerting adverse health effects. Their toxic properties may vary depending on their chemical form and solubility, which can be affected by aqueous processing during aerosol atmospheric lifetime. In this work, fine particulate matter (PM2.5) was collected in the city centre of Padua in the Po Valley (Italy), during a winter campaign. Part of the sampling filters were used to measure the kinetics by which metal ions and other elements can leach from PM2.5 to an aqueous solution mimicking fog water in the winter in temperate climate regions (pH 4.7, 5\ub0C). The leaching process was interpreted by a first order kinetics, and the fitting of the experimental data allowed to obtain the leaching kinetic constants and the equilibrium concentrations (i.e., at infinite time) for all elements. The remaining filter parts were mineralised, through two subsequent extraction steps, and the extracts were analysed by ICP-MS to gain the total elemental content of PM for a large number of elements. We found that elements can leach from PM with half times generally between 10\u201340 minutes, which is a timescale compatible with atmospheric aqueous processing during fog events. For instance, aluminium(III) in PM2.5 dissolved with an average k = 0.0185 min\u20131, and t1/2 = 37.5 min. Nevertheless, a fraction of each element was immediately solubilised after contact with the extraction solution suggesting that metal ion solubilisation may already had started during particle lifetime in the atmosphere

Quaternary ferrites by batch and continuous flow hydrothermal synthesis: a comparison

Crystalline spinel quaternary ferrites MxZn1−xFe2O4 (M = Co, Ni; x = 0.2, 0.35, 0.5, 0.65, 0.8) were synthesised through conventional batch hydrothermal synthesis (HT) at 135 °C as well as via continuous flow hydrothermal synthesis (CHFS). The as prepared compounds were thoroughly characterised from a compositional (ICP-MS, XPS) and structural (XRD) point of view in order to compare the synthetic approaches and achieve a greater understanding of how the chosen approach influences the characteristics of the resulting spinel

Vineyard pruning residues pellets for use in domestic appliances: A quality assessment according to the EN ISO 17225

Nowadays many types of biomass are studied to satisfy the increased demand of renewable energy based on pellet combustion. However, only a few biomasses fulfil the high quality standard required for pellet used in domestic appliances. European and International standards in force define this quality of non-industrial use of pellets in term of the origin of biomass, physical, mechanical and chemical parameters. Vineyard residues are a worldwide potential source of energy but their compliance to be used in domestic pellet stoves has not been yet proven according to the new standards in force. In order to meet this need, this study makes an exhaustive characterisation of vineyard based pellets manufactured from residues of Prosecco (Glera variety) vineyards, assessing both the quality of biofuel and its behaviour during combustion in a domestic pellet stove. The quality of biofuel has been evaluated according to the in force standards for wood and non-woody pellets. The results show that vineyard pellets do not meet the type B quality standards required for non-industrial use of wood pellet mainly because of the high amount of ash content (&gt;2%) and the high amount of copper (&gt;10 ppm) but they fulfil the specifications of the type B non-woody pellets. Furthermore, during combustion test of vineyard-based pellet the high emission of CO indicates incomplete combustion; and vineyard- based pellet NOx emissions are more than double compared to those obtained during the control tests, confirming that the analysed vineyard-based pellets are unsuitable, as they are, for use in traditional pellet stoves.</jats:p

When ring makes the difference: coordination properties of Cu2+/Cu+ complexes with sulfur-pendant polyazamacrocycles for radiopharmaceutical applications

Three polyazamacrocyclic ligands, i.e. 1,5,9-tris[2-(methylsulfanyl)ethyl]-1,5,9-triazacyclododecane (TACD3S), 1,4,7,10-tetrakis[2-(methylsulfanyl)ethyl]-1,4,7,10-tetrazacyclotridecane (TRI4S) and 1,4,8,11-tetrakis[2-(methylsulfanyl)ethyl]-1,4,8,11-tetrazacyclotetradecane (TE4S), were considered as potential chelators for the medically relevant copper radioisotopes. The ligands have been synthesized through facile, single-step reactions, and their acidity constants have been measured in aqueous solution at 25 degrees C. The kinetic, thermodynamic, electrochemical and structural properties of their Cu2+ and Cu+ complexes were investigated in aqueous solution at 25 degrees C using spectroscopic (UV-Visible, EPR, NMR) and electrochemical techniques (pH-potentiometric titrations, cyclic voltammetry and electrolysis). TACD3S was demonstrated to be unable to stabilize Cu2+, whereas for TRI4S and TE4S the formation of stable monocupric (CuL2+) and monocuprous (CuL+) complexes was detected. TRI4S coordinates Cu(2+)via a [4N] and a [4N]S array of donor atoms while with TE4S only the latter geometry exists. The thermodynamic stability and the kinetic inertness of the copper complexes formed by TACD3S, TRI4S and TE4S were compared with those previously reported for 1,4,7,10-tetrakis-[2-(methylsulfanyl)ethyl]-1,4,7,10-tetrazacyclododecane (DO4S) to unravel the influence of the ring size and the nitrogen donor array on the copper chelation properties of these sulfur-rich macrocycles. The copresence of four nitrogen atoms is an essential feature to allow effective copper coordination when a 12-member ring is employed, as the Cu2+-DO4S complexes were far more stable than those of Cu2+-TACD3S. Furthermore, the larger ring size of TRI4S and TE4S, when compared to DO4S, progressively increases the rate of the Cu2+ complexation reactions but decreases the thermodynamic stability of the Cu2+ complexes. Despite this, the ability of TRI4S and TE4S to stably accommodate both copper oxidation states makes them very attractive for application in nuclear medicine as they could avoid the demetallation after the biologically triggered Cu2+/Cu+ reduction

4D Multimodal Nanomedicines Made of Nonequilibrium Au-Fe Alloy Nanoparticles

Several examples of nanosized therapeutic and imaging agents have been proposed to date, yet for most of them there is a low chance of clinical translation due to long-term in vivo retention and toxicity risks. The realization of nanoagents that can be removed from the body after use remains thus a great challenge. Here, we demonstrate that nonequilibrium gold–iron alloys behave as shape-morphing nanocrystals with the properties of self-degradable multifunctional nanomedicines. DFT calculations combined with mixing enthalpy-weighted alloying simulations predict that Au–Fe solid solutions can exhibit self-degradation in an aqueous environment if the Fe content exceeds a threshold that depends upon element topology in the nanocrystals. Exploiting a laser-assisted synthesis route, we experimentally confirm that nonequilibrium Au–Fe nanoalloys have a 4D behavior, that is, the ability to change shape, size, and structure over time, becoming ultrasmall Au-rich nanocrystals. In vivo tests show the potential of these transformable Au–Fe nanoalloys as efficient multimodal contrast agents for magnetic resonance imaging and computed X-ray absorption tomography and further demonstrate their self-degradation over time, with a significant reduction of long-term accumulation in the body, when compared to benchmark gold or iron oxide contrast agents. Hence, Au–Fe alloy nanoparticles exhibiting 4D behavior can respond to the need for safe and degradable inorganic multifunctional nanomedicines required in clinical translation.Instituto de Investigaciones Fisicoquímicas Teóricas y AplicadasInstituto de Física La Plat

Reversible and high accuracy pH colorimetric sensor array based on a single acid-base indicator working in a wide pH interval

A pH colorimetric sensor array (CSA) with fast response time (<1 min) using only one acid-base indicator, Bromothymol Blue (BB), was prepared and characterized by modulating the amount, C, of the surfactant Hexadecyltrimethylammonium p-toluenesulfonate between 0 and 0.3725 gCTApTs/gprecursor with a constant amount of the OrMoSil precursors. The effect of the C increase is a continuous acidic shift of the calibration position, i.e. a huge variation of the pKa value of BB in the pH range 5.80-13.50. The precision error decreased with increasing C from 0.096 pH units (lower C values) to 0.023 pH units (larger C values). This result led to the development of a model to determine the number of spots with suitable C values required for having a similar value of precision in the entire working interval of the CSA. By selecting only 4 spots the precision error is < 0.100 pH units in the pH range 5.80\u201313.50. With 256 spots (diameter of each spot 48 3 mm), the model predicted an error almost constant ( 480.010) in the entire pH range

Influence of surfactant chain length, counterion and OrMoSil precursors on reversibility and working interval of pH colorimetric sensors

An in-depth study was conducted to determine the influence of some important parameters to produce a pH colorimetric sensor characterized by long-term stability, lack of leaching, high reversibility, repeatability and extended working range. Bromothymol Blue (BB) was used as pH sensitive molecule. Its performance was monitored while tailoring the concentration of some added cationic surfactants, together with the organic fraction of the sol-gel composition to avoid leaching phenomena, low homogeneity and to increase reversibility. Five cationic surfactants with different linear alkyl chain length (from C8 to C18) were added to a sol-gel containing BB. The C16 was chosen as optimal. The effect of the surfactant counterion was also investigated. The C16 surfactant had a pH working interval of 3 pH unit by using chloride, 1.5 with bromide and 1 pH unit with p-toluenesulfonate as counterions, respectively. Chloride was characterized by a larger inhomogeneity while p-toluenesulfonate gave homogeneity and high repeatability. The hexadecyltrimethylammonium p-toluenesulfonate was therefore chosen as the best surfactant. Leaching in alkaline medium was avoided by using the dodecyl moiety among three organic groups linked to the OrMoSil matrix (dodecyl, phenyl and methyl). Colorimetric sensor arrays made with these specifications remained stable and reversible for months

Determination of the relevant equilibrium constants working in pH Colorimetric Sensor Arrays (CSAs)

The rationalization of the behavior of pH Colorimetric Sensor Arrays, based on Bromophenol Blue embedded in tetraethyl orthosilicates-based matrices, was accomplished by calculating the thermodynamic constants of the reactions involved. The constants were determined in four matrices upon variation of the concentration of surfactant, indicator, and anionic species present in buffers and samples. Based on the values found, it was demonstrated that the variation of the surfactant concentration widened the working interval up to 1.80 and 5.30 pH units in the solution and one of the tested polymers, respectively. The competitive reaction between anionic species and cationic head-groups of the surfactant shifted the position of the calibration profile ​​up to 1.50 pH units in solution. For the CSA, the shift was 0.35 pH units for a large concentration of surfactant (0.1 M) and negligible at low concentrations (<0.01 M). The proposed mechanism allowed for a very good curve fitting in all conditions

High accuracy OrMoSil (Polyvinylidene Fluoride)-supported colorimetric sensor: Novel approach for the calculation of the pH prediction error

pH colorimetric sensors with prediction error comparable to the potentiometric measurements in the working range of the indicator employed, were prepared. Bromothymol Blue (BB), Tetrabromophenol Blue (TBB), Cresol Red (CR) and Brilliant Yellow (BY) in PVDF (Polyvinylidene Fluoride)-supported OrMoSil (organically modified silicate) matrix, were used. Sensor preparation was reproducible. Signal was based on a suitably modified Hue coordinate from HSV (Hue, Saturation, Value) color space, H. Although H profile was not influenced by the indicator concentrations, the prediction error depended on the product of saturation and luminance, \u394. By using H, the response of every spot was less affected by shape and optical inhomogeneity. The H calibration held for all the spots of the same lot and remained identical in time giving an advantage with respect to a glass electrode requiring calibration before each set of measurements. The prediction errors both in solution and in the OrMoSil matrix were similar: for BB, spHjavax.xml.bind.JAXBElement@315a8962 = 0.03 in both environments; for TBB, spHjavax.xml.bind.JAXBElement@4f058030 = 0.02 in the sensing spot and 0.05 in solution; for CR, spHjavax.xml.bind.JAXBElement@4ee5bdc0 = 0.11 in the sensing spot and 0.04 in solution; for BY, spHjavax.xml.bind.JAXBElement@36932dcd = 0.17 in the sensing spot and 0.07 in solution. Indeed, H values of TBB and BB increased their variances near the inflection point where \u394 has the minimum value (heteroscedastic behavior)

Kinetic response of pH colorimetric sensors: Role of the cationic surfactant concentration and amount and type of solvent used in the preparation of the sensing spot

A pH colorimetric sensor array (CSA) with a kinetic response comparable to those of the pH-meter was prepared. The signal comes from the Hue coordinate (H) and RGB profiles of some pH indicators such as Bromothymol Blue (BB) and Nitrazine Yellow (NY) in polyvinylidene fluoride (PVDF)-supported organically modified silicate (OrMoSil) spots. The t95 is of the order of 50\u2013150 s for RGB coordinates but is lowered of one order of magnitude employing the H coordinate as the detection signal. The addition of the Hexadecyltrimethylammonium p-toluenesulfonate (CTApTs) additive in the interval 0.10 0.19 gCTApTs/gprecursors, the transition from the basic to the acid form was hindered by the cationic interface due to the surfactant. The CTApTs concentrations, leading to a t95 lower than one minute, were in the interval 0.10 < R < 0.37 gCTApTs/gprecursors for NY and 0.10 < R < 0.28 gCTApTs/gprecursors for BB, comparable to the response time of the potentiometric measurements. Indeed, the kinetic profiles did not change with the amount and type of solvent