Abstract
The fate of the acidic organic solute from the soil-water-solvent system is not well-understood. In this study, the effect of the acidic functional group of organic solute in the sorption from cosolvent system was evaluated. The sorption of naphthalene (NAP) and 1-naphthoic acid (1-NAPA) by three kaolinitic soils and two model sorbents (kaolinite and humic acid) were measured as functions of the methanol volume fractions (f c ≤ 0.4) and ionic compositions (CaCl 2 and KCl). The solubility of 1-NAPA was also measured in various ionic compositions. The sorption data were interpreted using the cosolvency-induced sorption model. The K m values (= the linear sorption coefficient) of NAP with kaolinitic soil for both ionic compositions was log linearly decreased with f c. However, the K m values of 1-NAPA with both ionic compositions remained relatively constant over the f c range. For the model sorbent, the K m values of 1-NAPA with kaolinite for the KCl system and with humic acid for both ionic compositions decreased with f c, while the sorption of 1-NAPA with kaolinite for the CaCl 2 system was increased with f c. From the solubility data of 1-NAPA with f c, no significant difference was observed with the different ionic compositions, indicating an insignificant change in the aqueous activity of the liquid phase. In conclusion, the enhanced 1-NAPA sorption, greater than that predicted from the cosolvency-induced model, was due to an untraceable interaction between the carboxylate and hydrophilic soil domain in the methanol-water system. Therefore, in order to accurately predict the environmental fate of acidic pesticides and organic solutes, an effort to quantitatively incorporate the enhanced hydrophilic sorption into the current cosolvency-induced sorption model is required.
| Original language | English |
|---|---|
| Pages (from-to) | 22-29 |
| Number of pages | 8 |
| Journal | Journal of Environmental Science and Health - Part B Pesticides, Food Contaminants, and Agricultural Wastes |
| Volume | 47 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - 2012 Jan 1 |
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Keywords
- 1-Napthoic acid
- cosolvency
- kaolinitic soil
- sorption
ASJC Scopus subject areas
- Food Science
- Pollution
- Medicine(all)
Cite this
Sorption of acidic organic solute onto kaolinitic soils from methanol-water mixtures. / Kim, Juhee; Kim, Minhee; Hyun, Seunghun; Kim, Jeong-Gyu; Ok, Yong Sik.
In: Journal of Environmental Science and Health - Part B Pesticides, Food Contaminants, and Agricultural Wastes, Vol. 47, No. 1, 01.01.2012, p. 22-29.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Sorption of acidic organic solute onto kaolinitic soils from methanol-water mixtures
AU - Kim, Juhee
AU - Kim, Minhee
AU - Hyun, Seunghun
AU - Kim, Jeong-Gyu
AU - Ok, Yong Sik
PY - 2012/1/1
Y1 - 2012/1/1
N2 - The fate of the acidic organic solute from the soil-water-solvent system is not well-understood. In this study, the effect of the acidic functional group of organic solute in the sorption from cosolvent system was evaluated. The sorption of naphthalene (NAP) and 1-naphthoic acid (1-NAPA) by three kaolinitic soils and two model sorbents (kaolinite and humic acid) were measured as functions of the methanol volume fractions (f c ≤ 0.4) and ionic compositions (CaCl 2 and KCl). The solubility of 1-NAPA was also measured in various ionic compositions. The sorption data were interpreted using the cosolvency-induced sorption model. The K m values (= the linear sorption coefficient) of NAP with kaolinitic soil for both ionic compositions was log linearly decreased with f c. However, the K m values of 1-NAPA with both ionic compositions remained relatively constant over the f c range. For the model sorbent, the K m values of 1-NAPA with kaolinite for the KCl system and with humic acid for both ionic compositions decreased with f c, while the sorption of 1-NAPA with kaolinite for the CaCl 2 system was increased with f c. From the solubility data of 1-NAPA with f c, no significant difference was observed with the different ionic compositions, indicating an insignificant change in the aqueous activity of the liquid phase. In conclusion, the enhanced 1-NAPA sorption, greater than that predicted from the cosolvency-induced model, was due to an untraceable interaction between the carboxylate and hydrophilic soil domain in the methanol-water system. Therefore, in order to accurately predict the environmental fate of acidic pesticides and organic solutes, an effort to quantitatively incorporate the enhanced hydrophilic sorption into the current cosolvency-induced sorption model is required.
AB - The fate of the acidic organic solute from the soil-water-solvent system is not well-understood. In this study, the effect of the acidic functional group of organic solute in the sorption from cosolvent system was evaluated. The sorption of naphthalene (NAP) and 1-naphthoic acid (1-NAPA) by three kaolinitic soils and two model sorbents (kaolinite and humic acid) were measured as functions of the methanol volume fractions (f c ≤ 0.4) and ionic compositions (CaCl 2 and KCl). The solubility of 1-NAPA was also measured in various ionic compositions. The sorption data were interpreted using the cosolvency-induced sorption model. The K m values (= the linear sorption coefficient) of NAP with kaolinitic soil for both ionic compositions was log linearly decreased with f c. However, the K m values of 1-NAPA with both ionic compositions remained relatively constant over the f c range. For the model sorbent, the K m values of 1-NAPA with kaolinite for the KCl system and with humic acid for both ionic compositions decreased with f c, while the sorption of 1-NAPA with kaolinite for the CaCl 2 system was increased with f c. From the solubility data of 1-NAPA with f c, no significant difference was observed with the different ionic compositions, indicating an insignificant change in the aqueous activity of the liquid phase. In conclusion, the enhanced 1-NAPA sorption, greater than that predicted from the cosolvency-induced model, was due to an untraceable interaction between the carboxylate and hydrophilic soil domain in the methanol-water system. Therefore, in order to accurately predict the environmental fate of acidic pesticides and organic solutes, an effort to quantitatively incorporate the enhanced hydrophilic sorption into the current cosolvency-induced sorption model is required.
KW - 1-Napthoic acid
KW - cosolvency
KW - kaolinitic soil
KW - sorption
UR - http://www.scopus.com/inward/record.url?scp=84863337956&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84863337956&partnerID=8YFLogxK
U2 - 10.1080/03601234.2012.601949
DO - 10.1080/03601234.2012.601949
M3 - Article
VL - 47
SP - 22
EP - 29
JO - Journal of Environmental Science and Health - Part B Pesticides, Food Contaminants, and Agricultural Wastes
JF - Journal of Environmental Science and Health - Part B Pesticides, Food Contaminants, and Agricultural Wastes
SN - 0360-1234
IS - 1
ER -