Search results

Filters

  • Journals
  • Authors
  • Keywords
  • Date
  • Type

Search results

Number of results: 4
items per page: 25 50 75
Sort by:
Download PDF Download RIS Download Bibtex

Abstract

This work determined the solid-water distribution coefficient Kd, the Freundlich constant KF and the organic carbon normalized coefficient K0c of ibuprofen in natural, aquifer sediments. They are characterized as silt sediments with different clay and sand fraction contents varied in specific surface areas. Content of organic carbon and pH are on the same level. For determining sorption coefficients values of ibuprofen in sediments, its concentration was measured in the aqueous and calculated in the solid phase. Batch tests were conducted following OECD Guideline 106. The resulting Kd values ranged between 1.14 and 2.29 L/kg, ~ between 0.25 and 5.48 and Koc between 1.22 and 2.53 for ibuprofen in sediments SI and S2, respectively. These experiments proved that the presence of clay minerals beside organic carbon and pH might be relevant in sorption of ibuprofen in sediments. A comparison of experimentally determined Koc with modelled Koc calculated on the base of octanol-water partitioning coefficient K0w shows that the prediction of sorption behaviour cannot be based only on Kow· This is probably due to the fact that these approaches well describe hydrophobic interactions, but fail to predict sorption of polar and ionic compounds.
Go to article

Authors and Affiliations

Katarzyna Styszko
Katarzyna Sosonowska
Piotr Wojtanowicz
Janusz Gołaś
Jerzy Górecki
Mariusz Macherzyński
ORCID: ORCID
Download PDF Download RIS Download Bibtex

Abstract

In the study we have focused on the distribution of several metals (Cr, As, Pb) and anions (Cr, NO3-) and their partition between pore (interstitial) waters and sediments sampled at three stations at the Dobczyce Reservoir which supplies the drinking water to inhabitants from the city of Kraków and its agglomeration. The results show considerable increase in concentrations of Pb and As in pore water samples, when compared to the bottom waters. Meaningful alternations in concentration were observed in case of pore water samples (Pb, As) and sediments (Cr, Pb, As), coming from three stations and their lateral sections. The possible relations between this phenomenon and the sediment characteristic as well as the Fe and Ca content, has been studied. Some comments on the seasonal variations of anion contents in water and pore water samples, are also provided. It was found that nitrates and sulphates show considerable variations.
Go to article

Authors and Affiliations

Mariusz Macherzyński
ORCID: ORCID
Witold Reczyński
J. Sanecki
Jerzy Górecki
Janusz Gołaś
Download PDF Download RIS Download Bibtex

Abstract

Mercury is a highly toxic metal which naturally occurs in the Earth’s crust and has adverse effects on both humans and the environment. The use of fossil fuels for electricity generation and specific industries sources of mercury emissions. These emissions depend on the mercury content in fuels of different types, the process gas temperature and composition, the implementation of air pollutant control devices (APCDs), etc. The APCDs partially capture and/or oxidize mercury in flue gas as a side benefit. In some cases, the emissions are reduced by mercury-dedicated or mixed methods. Mercury transformation in process gases is generally based on a chain of homogeneous and/or heterogeneous reactions. The theory of gaseous mercury/solid phase reactions and its mechanisms is widely studied in the literature. In this review, we focused on the theoretical and practical studies of these mechanisms, including mercury oxidization and capture from specified laboratory simulated or process gases and industries. We summarized research on various reactions – mostly of a chemical type – between different forms of mercury derived from process gases, and solids, including particles of different kinds (fly ash, adsorbents or catalysts). We additionally reviewed the literature on the interactions between mercury and sulfur compounds in the simulated and process gases.
Go to article

Authors and Affiliations

Yinyou Deng
1
ORCID: ORCID
Mariusz Macherzyński
2
ORCID: ORCID

  1. AGH Doctoral School, AGH University of Science and Technology, Al. Mickiewicza 30, 30-059 Krakow
  2. AGH University of Science and Technology, Department of Coal Chemistry and Environmental Sciences, Faculty of Fuel and Energy, Al. Mickiewicza 30, 30-059, Krakow

This page uses 'cookies'. Learn more