• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 2006.04a
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• pp.115-118
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• 2006

The partitioning tracer method has been studied as an alternative method for characterizing aquifers contaminated by nonaqueous phase liquids (NAPLs). Accurate partition coefficients of tracers partitioning between NAPL and water are needed to improve the reliability of the partitioning tracer method. In this research, partition coefficients of alcohol tracers partitioning between benzene, toluene, ethylbenzene, and xylenes (BTEX) compounds and water are estimated from using the approach of equivalent alkane carbon number (EACN). General agreement was observed in between the measured and estimated partition coefficients. Based on these results we can verify that the EACN approach is suitable for estimating the partition coefficient.

• Journal of Soil and Groundwater Environment
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• v.12 no.2
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• pp.47-54
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• 2007

The partitioning tracer method has been studied as an alternative method for detecting and characterizing the distribution of nonaqueous phase liquids (NAPLs) contaminants in subsurface. The reliability of the partitioning tracer method depends on accurate measurements of partition coefficients of the partitioning tracers between water and NAPLs. In this study, partition coefficients of several alcohol tracers between water and benzene, toluene, ethylbenzene, xylene, and BTEX mixtures are estimated using the modified approach of equivalent alkane carbon number (EACN). Agreements between the measured and estimated partition coefficients were generally observed in experiments. Based on these results, it is confirmed that the partition coefficients of tracers are readily obtained without experiments if the EACN values for the tracers and LNAPLs are known.

• Journal of Radiation Industry
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• v.10 no.4
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• pp.181-187
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• 2016

Selective ${\beta}_1$-agonist and antagonists are used for the treatment of cardiac diseases including congestive heart failure, angina pectoris and arrhythmia. Selective ${\beta}_1$-antagonists including nebivolol have high binding affinity on ${\beta}_1$-adrenergic receptor, not ${\beta}_2$-receptor mainly expressed in smooth muscle. Nebivolol is one of most selective ${\beta}_1$-blockers in clinically used ${\beta}_1$-blockers including atenolol and bisoprolol. We tried to develop clinically useful cardiac PET tracers using a selective ${\beta}_1$-blocker. Nebivolol is $C_2$-symmetric and has two chromane moiety with a secondary amino alcohol and aromatic fluorine. We adopted the general synthetic strategy using epoxide ring opening reaction. Unlike formal synthesis of nebivolol, we prepared two chromane building blocks with fluorine and iodine which was transformed to diaryliodonium salt for labelling of $^{18}F$. Two epoxide building blocks were readily prepared from commercially available chromene carboxylic acids (1, 8). Then, the amino alcohol building block (15) was prepared by ammonolysis of epoxide (14) followed by coupling reaction with the other building block, epoxide (7). Diaryliodonium salt, a precursor for $^{18}F$-aromatic substitution, was synthesized in moderate yield which was readily subjected to $^{18}F$-aromatic substitution to give $^{18}F$-labelled nebivolol.