Investigation of arsenic removal from aqueous solution through selective sorption and nanofiber-based filters.

BACKGROUND: This research paper focuses on removing of arsenic from contaminated water via a nanofibrous polymeric microfiltration membrane, applied in prospective combination with an inorganic sorbent based on iron oxide hydroxide FeO(OH). MATERIALS AND METHODS: Nanofibrous materials were prepared by electrospinning from polyurethane selected by an adsorption test. The chemical composition (FTIR), morphology (SEM, porometry) and hydrophilicity (contact angle) of the prepared nanostructured material were characterized. The process of eliminating arsenic from the contaminated water was monitored by atomic absorption spectroscopy (AAS). The adsorption efficiency of the nanofibrous material and the combination with FeO(OH) was determined, the level of arsenic anchorage on the adsorption filter was assessed by a rinsing test and the selectivity of adsorption in arsenic contaminated mineral water was examined. RESULTS: It was confirmed that the hydrophilic aromatic polyurethane of ester type PU918 is capable of capturing arsenic by complexation on nitrogen in its polymer chains. The maximum As removal efficiency was around 62 %. Arsenic was tightly anchored to the polymeric adsorbent. The adsorption process was sufficiently selective. Furthermore, it was found that the addition of even a small amount of FeO(OH) (0.5 g) to the nanofiber filter would increase the efficiency of As removal by 30 %. CONCLUSIONS: The presented results showed that an adsorption filter based on a polyurethane nanostructured membrane added with an inorganic adsorbent FeO(OH) is a suitable way for the elimination of arsenic from water. However, it is necessary to ensure perfect contact between the surface of the nanostructure and the filtered medium.

The presence of fine and ultrafine particulate matter in the work environment.

This study presents the results of pilot measurement, where the exposure of fine and ultrafine particulate matter was monitored. The measurement was performed in welding workplace, where these particles are produced unintentionally. The measurement consisted of collecting information and measuring the concentration of particles in the workplace, where data collection was focused only on inhalation exposure. During welding, primarily 300 nm size particles are produced, and their concentration is strongly influenced by the welding material, type of welding and suction. The particles are amorphous in terms of morphology and contain manganese, iron and silicon, which can cause neurodegenerative diseases. Furthermore, the results indicate the importance of monitoring oral exposure.

Levels and Health Risk Assessment of PM10 Aerosol in Brno, Czech Republic.

OBJECTIVE: The main effort of this work was to evaluate the situation of the atmosphere in selected regions of Brno during the years 2009-2013 and to estimate health risks which might come up due to the increased concentrations of airborne particulate matter. METHODS: PM10 samples were collected in four areas varying in degree of automobile traffic using automatic and gravimetric sampling methods. PM10 concentrations were assessed using Spearman's rank correlation coefficient. Health risks were estimated based on calculation of relative risks and population for four health endpoints. The selected health outcomes were premature mortality, cardiovascular disease, respiratory disease, and chronic bronchitis. RESULTS: The highest PM10 concentrations were measured in two regions with high traffic loads T1, T2 and background region B2. The values were 34.33 ± 11.52 µg·m-3 in 2010, 34.87 ± 12.03 µg·m-3 in 2013 and 34.52 ± 8.81 µg·m-3 in 2009, respectively. The highest correlation was between T1 and T2 having Spearman's correlation coefficient 0.888 followed by T1-B1 pair with coefficient 0.886. For all health outcomes, the highest health effect of PM (E) was determined for T2 site in 2010 which was 48 ± 14, 49 ± 21, 44 ± 19 and 24 ± 10 for premature mortality, cardiovascular disease, respiratory disease, and chronic bronchitis, respectively. CONCLUSION: The concentrations are highly correlated, especially in traffic regions. The annual concentrations did not exceed the legislation limit but 24-hours limit was exceeded more than two times in several cases. The highest number of cases with a given health outcome was estimated in traffic regions especially for cardiovascular disease and premature mortality.

Levels, sources, and health risk assessment of polycyclic aromatic hydrocarbons in Brno, Czech Republic: a 5-year study.

This work aimed to determine the seasonal variations of polycyclic aromatic hydrocarbons (PAHs) in airborne PM10 at two background sites (Masná-MS, Lísen-LN) in Brno over a 5-year period (2009-2013). Samples were collected on quartz filters using a low-volume sampler by continual filtration. Concentrations of PAHs in collected PM10 samples were determined using a gas chromatography with a mass spectrometer as a detector. A different number of PAHs were determined to be at each site, i.e., 11 PAHs at the MS site and six PAHs at the LN site, and similarities between them were identified using non-parametric analysis of variance. Potential sources were identified using principal component analysis (PCA) and PAHs diagnostic ratios. The work also focused on health risk assessment. This was estimated using toxic equivalent factors to calculate individual lifetime cancer risk, which quantifies risk of exposure to PAHs for specific age groups. The average 11-PAH concentrations in M|S site annually ranged from 19.28 ± 19.02 ng m-3 (2011) to 40.37 ± 21.35 ng m-3 (2013). With regard to the LN site, the average six-PAH concentrations annually ranged from 3.64 ± 3.87 ng m-3 (2009) and 5.27 ± 6.19 ng m-3 (2012). PCA and diagnostic ratios indicate the main sources to be traffic emissions and coal combustion. Health risk assessment showed carcinogenic risk under limit value in all cases.

Dissolution kinetics of Pd and Pt from automobile catalysts by naturally occurring complexing agents.

Powder samples prepared from gasoline (Pt, Pd, Rh, new GN/old GO) and diesel (Pt, new DN/old DO) catalysts and recycled catalyst NIST 2556 were tested using kinetic leaching experiments following 1, 12, 24, 48, 168, 360, 720 and 1440-h interactions with solutions of 20mM citric acid (CA), 20 mM Na(2)P(4)O(7) (NaPyr), 1 g L(-1) NaCl (NaCl), a fulvic acid solution (FA-DOC 50 mg L(-1)) and 20 mM CA at pH 3, 4, 5, 6, 7, 8 and 9. The mobilisation of platinum group elements (PGEs) was fastest in solutions of CA and NaPyr. In the other interactions (NaCl, FA), the release of PGEs was probably followed by immobilisation processes, and the interactions were not found to correspond to the simple release of PGEs into solution. Because of their low concentrations, the individual complexing agents did not have any effect on the speciation of Pd and Pt in the extracts; both metals are present in solution as the complexes Me(OH)(2), Me(OH)(+). Immobilisation can take place through the adsorption of the positively charged hydroxyl complexes or flocculation of fulvic acid, complexing the PGEs on the surface of the extracted catalysts. The calculated normalised bulk released NRi values are similar to the reaction rate highest in the solutions of CA and NaPyr.