scholarly journals Qualitative and quantitative determination of water in airborne particulate matter

2012 ◽  
Vol 12 (10) ◽  
pp. 27367-27393
Author(s):  
S. Canepari ◽  
C. Farao ◽  
E. Marconi ◽  
C. Giovannelli ◽  
C. Perrino
Keyword(s):  
Particulate Matter ◽  
Chemical Composition ◽  
Quantitative Determination ◽  
Inorganic Ions ◽  
Airborne Particulate Matter ◽  
Dicarboxylic Acids ◽  
Atmospheric Particulate Matter ◽  
Simple Method ◽  
Field Samples

Abstract. This paper describes the optimization and validation of a new simple method for the quantitative determination of water in atmospheric particulate matter (PM). The analyses are performed by using a coulometric Karl-Fisher system equipped with a controlled heating device; different water contributions are separated by the application of an optimized thermal ramp (three heating steps: 50–120 °C, 120–180 °C, 180–250 °C). The analytical performance of the method was verified by using standard materials containing 5.55% and 1% by weight of water. The recovery was greater than 95%; the detection limit was about 20 μg. The method was then applied to NIST reference materials (NIST1649a, urban particulate matter) and to real PM10 samples collected in different geographical areas. In all cases the repeatability was satisfactory (10–15%). When analyzing the reference material, the separation of four different types of water was obtained. In real PM10 samples the amount of water and its thermal profile differed as a function of the chemical composition of the dust. Mass percentages of 3–4% of water were obtained in most samples, but values up to about 15% were reached in areas where the chemical composition of PM is dominated by secondary inorganic ions and organic matter. High percentages of water were also observed in areas where PM is characterized by the presence of desert dust. A possible identification of the quality of water released from the samples was tried by applying the method to some hygroscopic compounds that are likely contained in PM (pure SiO2, Al2O3, ammonium salts, carbohydrates and dicarboxylic acids) and by comparing the results with those obtained from field samples.

scholarly journals Qualitative and quantitative determination of water in airborne particulate matter

2013 ◽  
Vol 13 (3) ◽  
pp. 1193-1202 ◽  
Author(s):  
S. Canepari ◽  
C. Farao ◽  
E. Marconi ◽  
C. Giovannelli ◽  
C. Perrino
Keyword(s):  
Particulate Matter ◽  
Chemical Composition ◽  
Quantitative Determination ◽  
Inorganic Ions ◽  
Airborne Particulate Matter ◽  
Dicarboxylic Acids ◽  
Atmospheric Particulate Matter ◽  
Simple Method ◽  
Field Samples

Abstract. This paper describes the optimization and validation of a new simple method for the quantitative determination of water in atmospheric particulate matter (PM). The analyses are performed by using a coulometric Karl-Fisher system equipped with a controlled heating device; different water contributions are separated by the application of an optimized thermal ramp (three heating steps: 50–120 °C, 120–180 °C, 180–250 °C). The analytical performance of the method was verified by using standard materials containing 5.55% and 1% by weight of water. The recovery was greater than 95%; the detection limit was about 20 μg. The method was then applied to NIST Reference Materials (NIST1649a, urban particulate matter) and to real PM10 samples collected in different geographical areas. In all cases the repeatability was satisfactory (10–15%). When analyzing the Reference Material, the separation of four different types of water was obtained. In real PM10 samples the amount of water and its thermal profile differed as a function of the chemical composition of the dust. Mass percentages of 3–4% of water were obtained in most samples, but values up to about 15% were reached in areas where the chemical composition of PM is dominated by secondary inorganic ions and organic matter. High percentages of water were also observed in areas where PM is characterized by the presence of desert dust. A possible identification of the quality of water released from the samples was tried by applying the method to some hygroscopic compounds that are likely contained in PM (pure SiO2, Al2O3, ammonium salts, carbohydrates and dicarboxylic acids) and by comparing the results with those obtained from field samples.

scholarly journals Toxic Organic Contaminants in Airborne Particles: Levels, Potential Sources and Risk Assessment

2021 ◽  
Vol 18 (8) ◽  
pp. 4352
Author(s):  
Donatella Pomata ◽  
Patrizia Di Filippo ◽  
Carmela Riccardi ◽  
Federica Castellani ◽  
Giulia Simonetti ◽  
...  
Keyword(s):  
Risk Assessment ◽  
Particulate Matter ◽  
Organic Contaminants ◽  
Human Health Risk ◽  
Airborne Particulate Matter ◽  
Principal Component ◽  
Cardiovascular Effects ◽  
Atmospheric Particulate Matter ◽  
Emission Source ◽  
Size Fractions

In the last years, many studies have focused on risk assessment of exposure of workers to airborne particulate matter (PM). Several studies indicate a strong correlation between PM and adverse health outcomes, as a function of particle size. In the last years, the study of atmospheric particulate matter has focused more on particles less than 10 μm or 2.5 μm in diameter; however, recent studies identify in particles less than 0.1 μm the main responsibility for negative cardiovascular effects. The present paper deals with the determination of 66 organic compounds belonging to six different classes of persistent organic pollutants (POPs) in the ultrafine, fine and coarse fractions of PM (PM < 0.1 µm; 0.1 < PM < 2.5 µm and 2.5 < PM < 10 µm) collected in three outdoor workplaces and in an urban outdoor area. Data obtained were analyzed with principal component analysis (PCA), in order to underline possible correlation between sites and classes of pollutants and characteristic emission sources. Emission source studies are, in fact, a valuable tool for both identifying the type of emission source and estimating the strength of each contamination source, as useful indicator of environment healthiness. Moreover, both carcinogenic and non-carcinogenic risks were determined in order to estimate human health risk associated to study sites. Risk analysis was carried out evaluating the contribution of pollutant distribution in PM size fractions for all the sites. The results highlighted significant differences between the sites and specific sources of pollutants related to work activities were identified. In all the sites and for all the size fractions of PM both carcinogenic and non-carcinogenic risk values were below acceptable and safe levels of risks recommended by the regulatory agencies.

scholarly journals Recovery of Hg(0) from the Aqueous Hg(I/II) Present in Analyte Solution after Quantitative Determination of Iron

2013 ◽  
Vol 2013 ◽  
pp. 1-3
Author(s):  
Suman K. Giri ◽  
Nigamananda Das
Keyword(s):  
Aqueous Solutions ◽  
Quantitative Determination ◽  
Simple Method ◽  
Stoichiometric Amount ◽  
Analyte Solution

An easy and feasible approach to recover HgCl2, used in quantitative determination of iron values, as Hg(0) was described. Both Hg(I) and Hg(II), present in the solution after quantitative determination of iron, was completely reduced to Hg(0) by the addition of aluminium chips in more slightly excess than the stoichiometric amount. The purity of recovered Hg(0) was verified by comparing the value of density with pure mercury. This simple method may be useful to remove the mercury from other waste aqueous solutions before their discharge into the environment.

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