The influence of aerosol size and organic carbon content on gas/particle partitioning of polycyclic aromatic hydrocarbons (PAHs)

2002 ◽  
Vol 36 (7) ◽  
pp. 1205-1220 ◽  
Author(s):  
John H Offenberg ◽  
Joel E Baker
2020 ◽  
Author(s):  
Sampriti Chaudhuri ◽  
Gabriel Sigmund ◽  
Hary von Rautenkranz ◽  
Thorsten Hueffer ◽  
Thilo Hofmann

<p>Biochar is a versatile soil additive and CO<sub>2</sub> neutral or negative “green” sorbent. Biochar can improve the soil quality, water retention capacity, and is effective in binding contaminants. Previous studies showed that biochar is a suitable remediation option at sites with residual contamination and that it is particularly favorable in immobilizing organic polycyclic aromatic hydrocarbons (PAHs) and cadmium. To achieve remediation goals, however, careful assessment of the soil geochemistry (pH, background ions, organic carbon content), the nature of the contaminant, and the application rate need to be carried out. We have screened the sorption affinity of 11 different types of biochars and 2 activated carbons for selected heavy metals and ionizable and non-ionizable PAHs. The biochars differed in the starting feedstock material (rice husk, wheat straw pellets, mixed softwood pellets, oil seed rape straw, miscanthus straw pellets), temperature of production (550°C, 700°C), and elemental composition. The target contaminants included acenaphthene, dibenzofuran, carbazole, dibenzothiophene, 2-hydroxybiphenyl, cadmium, and mercury. The sorption of the organic contaminants was driven by the carbon content, specific surface area, and aromatic nature of the biochars. Sorption of cadmium was higher onto biochars with greater inorganic fractions, whereas for mercury no specific trends could be observed. Based on the results of the initial screening, a novel approach to statistically design experiments using the Box-Behnken model was employed for selected biochars. Using this method, experiments were conducted to systematically investigate the influence of four factors (pH, dissolved organic carbon, ionic strength and contaminant concentration) on sorption at three different levels (-1, 0, +1). The results from the surface response modeling approach provides fundamental new insight into the applicability of these biochars at contaminated sites and can help identify scenarios favorable for remediation with biochar. Our results will help in the development of a remediation strategy with an overall low environmental footprint for contaminated soils.</p>


1991 ◽  
Vol 23 (1-3) ◽  
pp. 427-436 ◽  
Author(s):  
Y. Shimizu ◽  
H. M. Liljestrand

A fluorescence quenching method was used to determine the sorption of polycyclic aromatic hydrocarbons (PAHs) onto natural solids in batch experiments. This method is based upon the observation that PAHs fluoresce in aqueous solution but not when associated with natural solids. It avoids problems of incomplete solid-liquid separation. As natural solids, eleven different USEPA soils and sediments were used. Anthracene and 2-aminoanthracene, which are respectively non-ionic and ionic PAHs, were chosen as sorbates. The fractional decrease in fluorescence intensity as a function of added natural solid concentration is referred to as Stem-Volmer plots. The plots were linear for all natural solids investigated. The conditional sorption coefficients (Ksc) at pH 6 through 8 and I=0.1 M were obtained as the slopes of the plots. While the Ksc values of anthracene were independent of pH, the values of 2-aminoanthracene decreased with increasing pH. The Ksc values of anthracene correlated well with the organic carbon content of natural solids. However, the values of 2-aminoanthracene did not depend on the content of organic carbon in natural solids. For 2-aminoanthracene, inorganic matrices of the natural solids may contribute to the sorption.


2008 ◽  
Vol 3 (No. 4) ◽  
pp. 231-240 ◽  
Author(s):  
E. Hiller ◽  
Ľ. Jurkovič ◽  
M. Bartaľ

The knowledge of sorption-desorption processes of polycyclic aromatic hydrocarbons (PAHs) in natural solids is essential to predict the fate, transport, and environmental risks of these pollutants. In this study, the effect was investigated of temperature on the sorption-desorption of three PAHs (naphthalene, phenanthrene, and pyrene) in two natural solids with different organic carbon contents. In all cases, the sorption isotherms obtained could be well described by the linear sorption model. The analysis based on the measured isotherms and the corresponding equilibrium partition coefficients (Kp) revealed that (1) the sorption of PAHs increased with organic carbon content of the solid and PAH hydrophobicity in the order: sediment < soil and naphthalene < phenanthrene < pyrene, respectively, and (2) the extent of PAH sorption decreased with increasing temperature from 4°C to 27°C on average by 27.3, 17.0, and 27.4% for naphthalene, phenanthrene, and pyrene, respectively. The enthalpies of sorption (δHs) calculated by van’t Hoff equation were negative, relatively small, and in the range of weak forces such as van der Waals forces (0–9 kJ/mol), consistent with hydrophobic interactions and partitioning of the PAHs into soil/sediment organic matter. The desorption of naphthalene and phenanthrene showed significant hysteresis, i.e. great fraction of PAHs was resistant to desorption and somewhat increased with temperature.


Molecules ◽  
2020 ◽  
Vol 25 (16) ◽  
pp. 3727
Author(s):  
Łukasz Dąbrowski

For complex matrices such as environmental samples, there is usually a problem with not fully resolved peaks during GC/MS analysis. The PARADISe computer program (based on the PARFAC2 model) allows the identification of peaks using the deconvoluted mass spectra and the NIST MS library. The number of repetitions required by this software (at least five) is a real limitation for the determination of semi-volatile compounds, like polycyclic aromatic hydrocarbons, polychlorinated biphenyls, and organic pesticides in environmental samples. In this work, the method to overcome this condition was proposed and evaluated. The sets of the five files required by PARADISe were prepared by mathematically modifying the original GC/MS chromatograms obtained for the standard mixture (C = 2 µg/mL of 40 compounds) and real sample extracts (soil samples with different total organic carbon content and one cardboard extract) spiked with standards. Total average match factor for all the substances identified in a standard mixture was 874 (near 900—“excellent match”), and for all the substances in the real samples, it was 786 (near 800—“good match”). The results from PARADISe were comparable to those obtained with other programs: AMDIS (NIST) and MassHunter (Agilent), tested also in this work. PARADISe software can be effectively used for chromatogram deconvolution and substance identification.


2009 ◽  
Vol 43 (17) ◽  
pp. 2693-2699 ◽  
Author(s):  
Diana Guzmán-Torres ◽  
Arantza Eiguren-Fernández ◽  
Pablo Cicero-Fernández ◽  
Marisela Maubert-Franco ◽  
Armando Retama-Hernández ◽  
...  

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