A Short Review of Simple Analytical Methods for the Evaluation of PAHs and PAEs as Indoor Pollutants in House Dust Samples

Studies on indoor air quality are indispensable when considering that people spend approximately 85% of their time in confined environments. This short review mostly takes into consideration research that uses passive samplers to evaluate the quality of indoor environments (houses, school, cars, etc.). This short review summarizes most analytical methods to detect and quantify PAHs and PAEs in house dust used as a passive sampler. The objective of house dust analysis is to identify the presence, amount and distribution of specific hazardous substances in confined spaces and, if possible, to identify their sources. Household dust and the compounds present in it can enter the human body by inhalation, non-food ingestion and absorption through the skin. The observed differences in concentrations of house dust may also indicate important differences in the chemical and physical nature of pollutants caused by air filtration and absorption during the migration of ambient air into the indoor environment

Analytical Method for Quantification of Several Phthalate Acid Esters by Gas Chromatography-Mass Spectrometry in Coffee Brew Samples

Several phthalate acid esters (PAEs), often called phthalate esters or phthalates, are substances classified as harmful due to their carcinogenic and mutagenic properties, and moreover, as dangerous for humans because they interfere with the endocrine system. In general, phthalic esters are used as plasticizers for different polymers and more other consumer products. In the present study, we describe a simple method to quantify PAEs in coffee brew using a liquid-liquid extraction without purification processes through analysing the obtained organic phase by GCMS in the single ion monitoring mode. The totals of single PAEs, in coffee brew samples analysed by us, are in the range of 159-5305 mu g L-1. Considering that, on average, a person drinks three cups (total 90 mL) of the aforementioned drink per day, this will lead to the uptake of a total 14 to 477 mu g of phthalates

Determination of selected phthalates by gas chromatography\u2013mass spectrometry in mural paintings from Palermo (Italy)

Phthalate esters for decades, and probably even now, were used as softeners in water-based paintings. In general, these compounds are dangerous owing to their carcinogenicity and reproductive effects. Phthalates are not chemically but only physically bound to the matrices, hence, they may be leached into the environment and are ubiquitously found in environmental matrices. Considering that, construction is one of most important\ufb01elds in Europe, and probably worldwide, with respect to its economic, technological and environmental impact. In the present work the phthalate esters content of several mural paintings was evaluated by gas chromatography\u2013 mass spectrometry (GC-MS). Because, this issue is especially important to ensure proper security measurements during processes that could involve particulate inhalation, the total concentrations of 15 compounds in the analyzed mural paintings, ranged from 0.8 to 236 mg/Kg d.w. with anaverage of 39.4 mg/Kg d.w. The highest concentration was found in a mural painting sampled in an apartment built about 50 years ago, though, building age was not signi\ufb01cantly correlated with the levels of total and single PAEs. Among the monitored phthalates, only four (bis(2-ethylhexyl) phthalate, diisobutyl phthalate, Di-n-butyl phthalate and diethyl phthalate) were detected in appreciable quantities. Benzyl butyl phthalate was relevant only for one sample and, at trace levels, only for two samples. In all tested mural paintings, except two samples, predominates the bis(2-ethylhexyl) phthalate (DEHP) (from 30 to 100% of total). In general, occasionally, dinonyl phthalate (DNP) was used as an alternative to DEHP, however, in our case, its occurrence was not found. Diisobutyl phthalate (DiBP) was detected in seven samples and ranged from 0.17 to 13.2 mg/Kg d.w

Diallyldimethylammonium Chloride (DADMAC) in Water Treated with Poly-Diallyldimethylammonium Chloride (PDADMAC) by Reversed-Phase Ion-Pair Chromatography—Electrospray Ionization Mass Spectrometry

Poly-diallyldimethylammonium (PDADMAC) chloride is a flocculant agent extensively used in water clarification treatments. Commercial polyelectrolyte formulations often contain residual monomer (DADMAC), reaction by-products and other reactants as contaminants that could potentially affect human health. In the present study, we optimized an analytical method based on reversed-phase ion-pair chromatography coupled with mass spectrometry for quantifying ultra-trace levels of DADMAC, without preliminary treatments, in drinking water distributed by the Palermo aqueduct. The method was validated in terms of accuracy (recovery between 80 to 120%), precision (RSD < 10%), linearity range (from 0.5 to 15 µg/L), limit of quantification and limit of detection (LOQ 0.42 µg/L and LOD 0.12 µg/L). DADMAC was detected in all analysed water samples and the concentration ranged from 1.2 to 3.8 µg/L whit a mean value of 1.7 µg/L. To the best of our knowledge, this paper represents the first study concerning DADMAC concentration in water samples collected in Italy and, in this context, this paper can be considered very interesting when comparing future data on DADMAC monitoring in water. Moreover, this is one of a few cases where DADMAC was found in drinking water

Determination of Selected Polyaromatic Hydrocarbons by Gas Chromatography-Mass Spectrometry for the Analysis of Wood to Establish the cause of Sinking of an Old Vessel (Scauri wreck) by Fire

The aimof this paper was to establish the cause of sinking of an old wooden vessel by polycyclic aromatic hydrocarbon (PAH) analyses because wood combustion is a source of PAHs. In particular, the molecular PAH patterns generated by each source are like fingerprints and it is possible to determine the processes that generate PAHs by studying their distribution in wood samples. The relative abundance of high molecular weight PAHs, together with the PAH compound ratios and with total index (proposed by us) has demonstrated that samples owe their PAHs in wood archaeological material to a predominant single mode of origin, i.e. combustion processes, therefore we can say that the sinking of the vessel was caused by a fire

Metals distribution in the organic and inorganic fractions of soil: a case study on soils from Sicily

AbstractThe content of Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb and Zn, has been determined in the organic and inorganic fraction of eight soil samples from Sicily. A modified type-Tessier sequential extraction procedure has been used to recognize metals in five different fractions categorised as follows: (a) exchangeable metals, (b) metals bound to carbonates, (c) metals bound to iron and manganese oxides, (d) metals bound to organic matter, and (e) metals in residual fraction. The mineralogical composition of soils samples was characterized by X-ray diffraction. Humic substances were extracted by means of an alkaline extraction procedure. It has been found that both the mineralogical composition and the different content of humic fraction of organic matter in the soils investigated are responsible for the observed trace metal distribution. The obtained data show that a significant amount of trace metals is bound to the organic fraction where different binding sites are present simultaneously. In particular, Pb an..

Synthesis, properties, antitumor and antibacterial activity of new Pt(II) and Pd(II) complexes with 2,2'-dithiobis(benzothiazole) ligand

Mono- and binuclear Pt(II) and Pd(II) complexes with 2,20-dithiobis(benzothiazole) (DTBTA) ligand are reported. [Pt(DTBTA)(DMSO)Cl]Cl 19CHCl3 (1) and [Pd2(m-Cl)2(DTBTA)2]Cl2 (2) have been synthesized and structurally characterized by elemental analysis, IR, 1H and 13C NMR spectroscopy, MS spectrometry and the content of platinum and palladium was determined using a flame atomic spectrometer. Two different coordination modes of 1 and 2 complexes were found; in both complexes, the coordination of Pt(II) and Pd(II) ions involves the N(3) atoms of the ligand but the binuclear complex 2, is a cis-chloro-bridged palladium complex. Evaluation of their in vitro antitumor activity against two human tumor cell lines human breast cancer (MCF-7) and hepatocellular carcinoma (HepG2); and their antimicrobial activity against Escherichia coli and Kokuria rhizophila was performed. Only complex 1 showed a dose- and time-dependent cytotoxic activity against the two tumor cell lines, associated to apoptosis and accumulation of treated cells in G0/G1 phase of cell cycle, while both 1 and 2 exhibited antimicrobial activity with complex 1 much more potent. The study on intracellular uptake in both MCF-7 and HepG2 cell lines revealed that only platinum of complex 1 is present inside the cells, suggesting a different mode of action of the two compounds. This was also in agreement with the results obtained for the antitumor and antibacterial activity

Seismicity and Focal Mechanisms at the Calabro-Lucanian boundary along the Apennine chain (southern Italy)

The Calabro-Lucanian boundary is a complex geological zone marking the transition between the highly seismogenic tectonic domains of Southern Apennines and the Calabrian Arc. Historical catalogues include earthquakes with macroseismic effects up to VII-VIII MCS (CPTI WORKING GROUP, 2004) and paleoseismological investigations suggested that earthquakes of magnitude between 6.5 and 7 may have occurred in this area, between the 6th and the 15th century (MICHETTI et alii, 2000). More recently, on 9 September 1998, an earthquake of moment magnitude M5.6 occurred at the north-western margin of the Pollino massif (GUERRA et alii, 2005; ARRIGO et alii, 2006) and since the second half of 2010 the same region was interested by a noteworthy seismic activity characterized by several swarms with thousands of events with a maximum magnitude of 3.6

Testing the stability of moment tensor solutions for small earthquakes in the Calabro-Peloritan Arc region (southern Italy)

The aim of this study is to test the stability of moment tensor solutions for crustal earthquakes in the Calabro-Peloritan area (southern Italy). We used waveforms recorded by the Italian National Seismic Network managed by the Istituto Nazionale di Geofisica e Vulcanologia and the CAT-SCAN (Calabria Apennine Tyrrhenian - Subduction Collision Accretion Network) project. We computed the moment tensor solutions using the Cut And Paste (CAP) method. The technique allows the determination of the source depth, moment magnitude and focal mechanisms using a grid search technique. For the earthquakes investigated, we tried different station distributions and different velocity models. Results were also checked by computing the moment tensor solutions using the SLUMT grid-search method. Both methods (CAP and SLUMT) allow time shifts between synthetic and observed data in order to reduce the dependence of the solution on the assumed velocity model and on earthquake location errors. Comparisons have been made with the available published solutions. The final focal mechanisms were robustly determined. We show that the application of the CAP and SLUMT methods can provide good-quality solutions in a magnitude range not properly represented in the Italian national earthquake catalogues, and where the solutions estimated from Ponset polarities are often poorly constrained