TY - JOUR
T1 - Selectivity of electron-donor- and electron-acceptor-bonded silica packing materials for hydrophobic environmental contaminants in polar and non-polar eluents
AU - Kimata, Kazuhiro
AU - Hosoya, Ken
AU - Kuroki, Hiroaki
AU - Tanaka, Nobuo
AU - Barr, John R.
AU - McClure, P. Cheryl
AU - Patterson, Donald G.
AU - Jakobsson, Eva
AU - Bergman, Ake
N1 - Funding Information:
This work was supported in part by a Monbusho International Joint Research Program and a Grant-in-Aid for Scientific Research funded by the Ministry of Education, Science, Sports, and Culture, Japan. The authors thank Beckman Instrument Co. for the loan of the equipment, 126 pump and 168 photodiode array detector with NUVEAU software.
PY - 1997/10/31
Y1 - 1997/10/31
N2 - Electron-acceptor-bonded stationary phases, 2-(nitrophenyl)ethylsilyl (NPE) and 3-(p-nitrophenoxy)propylsilyl (NPO), and electron-donor-bonded phases, 3-(N-carbazolyl)propylsilyl (CZP), 2-(1-pyrenyl)ethylsilyl (PYE), and 5-coronenylpentylsilyl (COP), were prepared from silica particles and their selectivities were examined in both polar and non-polar solvents for specific isomers of polychlorodibenzo-p-dioxins (PCDDs), hexachloronaphthalenes (HxCNs) and planar and non-planar polychlorobiphenyl (PCB) congeners. Although no single stationary phase was able to separate all the isomer pairs that are coproduced during the synthesis of the PCDDs and HxCNs, pairs can be separated by selecting a suitable stationary phase and solvent. The separation of mixtures of PCDD isomers were found to be most successful with PYE and NPO phases, which yielded the opposite elution orders for each isomer pair that is produced as a mixture. Similar results were obtained for the HxCN isomers that were separated on PYE and CZP phases. The COP phase provided easier separation of non-ortho-substituted and mono-ortho- substituted PCBs from the other PCBs based on the planarity than PYE phase.
AB - Electron-acceptor-bonded stationary phases, 2-(nitrophenyl)ethylsilyl (NPE) and 3-(p-nitrophenoxy)propylsilyl (NPO), and electron-donor-bonded phases, 3-(N-carbazolyl)propylsilyl (CZP), 2-(1-pyrenyl)ethylsilyl (PYE), and 5-coronenylpentylsilyl (COP), were prepared from silica particles and their selectivities were examined in both polar and non-polar solvents for specific isomers of polychlorodibenzo-p-dioxins (PCDDs), hexachloronaphthalenes (HxCNs) and planar and non-planar polychlorobiphenyl (PCB) congeners. Although no single stationary phase was able to separate all the isomer pairs that are coproduced during the synthesis of the PCDDs and HxCNs, pairs can be separated by selecting a suitable stationary phase and solvent. The separation of mixtures of PCDD isomers were found to be most successful with PYE and NPO phases, which yielded the opposite elution orders for each isomer pair that is produced as a mixture. Similar results were obtained for the HxCN isomers that were separated on PYE and CZP phases. The COP phase provided easier separation of non-ortho-substituted and mono-ortho- substituted PCBs from the other PCBs based on the planarity than PYE phase.
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U2 - 10.1016/S0021-9673(97)00597-9
DO - 10.1016/S0021-9673(97)00597-9
M3 - Article
C2 - 9408988
AN - SCOPUS:0030840209
SN - 0021-9673
VL - 786
SP - 237
EP - 248
JO - Journal of Chromatography
JF - Journal of Chromatography
IS - 2
ER -