Abstract
Abstract
This study reports results on the estimated magnitude of changes in P sorption isotherms in clayey mud sediments when performed using (1) freeze-dried instead of fresh sediment samples and (2) artificial sea water (ASW) instead of ambient near-bottom water. The sediments used differed in their P sorption. For the isotherms, sediments were equilibrated for 48 h in solutions of varying P concentration whereafter the amount of P sorbed or desorbed was determined. We adjusted the modified Freundlich equation to the isotherm data and assessed differences in the isotherms between the treatments by comparing equilibrium P concentrations and P buffering capacities determined from the isotherm equation. Freeze-drying decreased the P sorption in all investigated sediments, but the magnitude of the changes varied depending on the properties of the sediments. The effect was minor in the sediment abundant in P sorption sites and low in easily exchangeable P, while it was clearer in the sediments originally high in P or low in sorption surfaces. ASW and ambient water produced similar isotherms suggesting that ASW is a suitable equilibrium solution in P exchange experiments with muddy clay sediments. This study enlightens the processes occurring in freeze-drying. The results highlight that when examining the effects of dissimilar treatments or experimental conditions on the P exchange isotherms the magnitude and significance of the observed changes should be evaluated in a proper context considering the precision of the method.
Article highlights
The effects of freeze-drying on P sorption isotherms are minor in sediments abundant in unoccupied sorption surfaces.
Artificial sea water is a suitable background matrix for the P exchange isotherms.
The precision of the method should be considered when comparing the effects of differing isotherm treatments.
Funder
Maj ja Tor Nesslingin Säätiö
Publisher
Springer Science and Business Media LLC
Subject
General Earth and Planetary Sciences,General Physics and Astronomy,General Engineering,General Environmental Science,General Materials Science,General Chemical Engineering