skip to main content
OSTI.GOV title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: Naphthalene sorption to organic soil materials studied with continuous stirred flow experiments

Abstract

Estimation of sorption-desorption kinetics of hydrophobic contaminants in soils and sediments is a prerequisite for assessing the risk of hazardous compounds and for studying the feasibility of bioremediation treatments. Naphthalene sorption studies were carried out with four organic soil materials, using a batch sorption technique and a continuously stirred flow (CSF) cell. Reproducibility of the CSF experiments were tested, and an experiment with different inputs showed that experimental results were independent of input pulse length. Single-particle and multi-particle linear driving force models and bicontinuum models were tested. When the sorption coefficient K{sub om} was fixed at the values obtained from the batch experiments, the RMSE modeling error increased with increasing N{sub 2} surface area, S{sub N2}, of the soil materials. The high RMSE for soil materials with a high N{sub 2} surface area was the result of strong sorption-desorption non-singularity, most probably due to a larger fraction of the applied naphthalene diffusing to slow sorption sites. A dual resistance sorption model was able to accurately describe the data with two free parameters. However, parameter uncertainty resulted from the simultaneous optimization of the rate parameter, {alpha}, and K{sub om}. The combination of batch sorption experiments, input-response experiments, and model exercises givemore » supporting evidence that sorption kinetics of hydrophobic organic compounds to soil OM are controlled by (i) rapid pore diffusion toward S{sub N2} ({alpha} = 0.1 h{sup {minus}1}) and (ii) slow diffusion into the soil organic matter structure ({alpha} = 0.01--0.001 h{sup {minus}1}).« less

Authors:
 [1]; ;  [2]
  1. Danish Inst. of Agricultural Sciences, Tjele (Denmark). Dept. of Crop Physiology and Soil Science
  2. Univ. of Amsterdam (Netherlands). Dept. of Physical Geography and Soil Science
Publication Date:
Sponsoring Org.:
USDOE
OSTI Identifier:
678087
Resource Type:
Journal Article
Journal Name:
Soil Science Society of America Journal
Additional Journal Information:
Journal Volume: 63; Journal Issue: 2; Other Information: PBD: Mar-Apr 1999
Country of Publication:
United States
Language:
English
Subject:
54 ENVIRONMENTAL SCIENCES; SOILS; NAPHTHALENE; SORPTION; ORGANIC MATTER; SOIL CHEMISTRY; MATHEMATICAL MODELS; ENVIRONMENTAL TRANSPORT

Citation Formats

Jonge, H de, Heimovaara, T J, and Verstraten, J M. Naphthalene sorption to organic soil materials studied with continuous stirred flow experiments. United States: N. p., 1999. Web. doi:10.2136/sssaj1999.03615995006300020007x.
Jonge, H de, Heimovaara, T J, & Verstraten, J M. Naphthalene sorption to organic soil materials studied with continuous stirred flow experiments. United States. https://doi.org/10.2136/sssaj1999.03615995006300020007x
Jonge, H de, Heimovaara, T J, and Verstraten, J M. 1999. "Naphthalene sorption to organic soil materials studied with continuous stirred flow experiments". United States. https://doi.org/10.2136/sssaj1999.03615995006300020007x.
@article{osti_678087,
title = {Naphthalene sorption to organic soil materials studied with continuous stirred flow experiments},
author = {Jonge, H de and Heimovaara, T J and Verstraten, J M},
abstractNote = {Estimation of sorption-desorption kinetics of hydrophobic contaminants in soils and sediments is a prerequisite for assessing the risk of hazardous compounds and for studying the feasibility of bioremediation treatments. Naphthalene sorption studies were carried out with four organic soil materials, using a batch sorption technique and a continuously stirred flow (CSF) cell. Reproducibility of the CSF experiments were tested, and an experiment with different inputs showed that experimental results were independent of input pulse length. Single-particle and multi-particle linear driving force models and bicontinuum models were tested. When the sorption coefficient K{sub om} was fixed at the values obtained from the batch experiments, the RMSE modeling error increased with increasing N{sub 2} surface area, S{sub N2}, of the soil materials. The high RMSE for soil materials with a high N{sub 2} surface area was the result of strong sorption-desorption non-singularity, most probably due to a larger fraction of the applied naphthalene diffusing to slow sorption sites. A dual resistance sorption model was able to accurately describe the data with two free parameters. However, parameter uncertainty resulted from the simultaneous optimization of the rate parameter, {alpha}, and K{sub om}. The combination of batch sorption experiments, input-response experiments, and model exercises give supporting evidence that sorption kinetics of hydrophobic organic compounds to soil OM are controlled by (i) rapid pore diffusion toward S{sub N2} ({alpha} = 0.1 h{sup {minus}1}) and (ii) slow diffusion into the soil organic matter structure ({alpha} = 0.01--0.001 h{sup {minus}1}).},
doi = {10.2136/sssaj1999.03615995006300020007x},
url = {https://www.osti.gov/biblio/678087}, journal = {Soil Science Society of America Journal},
number = 2,
volume = 63,
place = {United States},
year = {Mon Mar 01 00:00:00 EST 1999},
month = {Mon Mar 01 00:00:00 EST 1999}
}