001     57080
005     20180211175451.0
024 7 _ |2 pmid
|a pmid:17540387
024 7 _ |2 DOI
|a 10.1016/j.chroma.2007.05.038
024 7 _ |2 WOS
|a WOS:000248107200028
037 _ _ |a PreJuSER-57080
041 _ _ |a eng
082 _ _ |a 540
084 _ _ |2 WoS
|a Biochemical Research Methods
084 _ _ |2 WoS
|a Chemistry, Analytical
100 1 _ |a Babay, P. A.
|b 0
|0 P:(DE-HGF)0
245 _ _ |a Column temperature as an active variable in the isocratic, normal-phase high-performance liquid chromatography separation of lipophilic metabolites of nonylphenol ethoxylates
260 _ _ |a New York, NY [u.a.]
|b Science Direct
|c 2007
300 _ _ |a 227 - 236
336 7 _ |a Journal Article
|0 PUB:(DE-HGF)16
|2 PUB:(DE-HGF)
336 7 _ |a Output Types/Journal article
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336 7 _ |a Journal Article
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|2 EndNote
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a article
|2 DRIVER
440 _ 0 |a Journal of Chromatography A
|x 0021-9673
|0 3154
|v 1157
500 _ _ |a Record converted from VDB: 12.11.2012
520 _ _ |a Normal-phase separation of technical grade nonylphenol (t-NP, about 90% 4-nonylphenol), 4-nonylphenol mono-ethoxylate (4-NP1EO) and 4-nonylphenol di-ethoxylate (4-NP2EO) was assessed, with the inclusion of column temperature as an active variable. The compound 2,4,6-trimethylphenol was evaluated for use as internal standard. Isocratic elution with 2-propanol/hexanes mixtures from an amino-silica column and spectrometric UV detection at 277 nm were employed. Technical nonylphenol presented a significant contribution from unknown substances that eluted with retention times similar to that of 4-NP1EO. GC-MS analysis of the unknowns allowed to identify them as isomers of 2-NP. The response of the system to joint variations in flow rate, eluent composition and column temperature was investigated by means of Doehlert statistical experimental design. A model for retention of the analytes as a function of the experimental variables was proposed, and separation selectivity was studied. Selection of the optimal working zone was made through desirability function (D) calculations. Potential co-elution of 2-NP isomers with 4-NP1EO was considered when optimizing the separation. The occurrence of a restricted region of the experimental space where baseline resolution of analytes, associated impurities and internal standard results feasible (D not equal to 0) is apparent.
536 _ _ |a Terrestrische Umwelt
|c P24
|2 G:(DE-HGF)
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|x 0
588 _ _ |a Dataset connected to Web of Science, Pubmed
650 _ 2 |2 MeSH
|a Chromatography, High Pressure Liquid: instrumentation
650 _ 2 |2 MeSH
|a Ethylene Glycols: isolation & purification
650 _ 2 |2 MeSH
|a Ethylene Glycols: metabolism
650 _ 2 |2 MeSH
|a Sensitivity and Specificity
650 _ 2 |2 MeSH
|a Spectrophotometry, Ultraviolet
650 _ 2 |2 MeSH
|a Temperature
650 _ 7 |0 0
|2 NLM Chemicals
|a Ethylene Glycols
650 _ 7 |0 27986-36-3
|2 NLM Chemicals
|a terics
650 _ 7 |a J
|2 WoSType
653 2 0 |2 Author
|a nonylphenol ethoxylates
653 2 0 |2 Author
|a lipophilic metabolites
653 2 0 |2 Author
|a normal-phase HPLC
653 2 0 |2 Author
|a column temperature
653 2 0 |2 Author
|a separation selectivity
700 1 _ |a Gettar, R. T.
|b 1
|0 P:(DE-HGF)0
700 1 _ |a Magallanes, J.F.
|b 2
|0 P:(DE-HGF)0
700 1 _ |a Becquart, E.T.
|b 3
|0 P:(DE-HGF)0
700 1 _ |a Thiele, B.
|b 4
|u FZJ
|0 P:(DE-Juel1)129410
700 1 _ |a Batistoni, D. A.
|b 5
|0 P:(DE-HGF)0
773 _ _ |a 10.1016/j.chroma.2007.05.038
|g Vol. 1157, p. 227 - 236
|p 227 - 236
|q 1157<227 - 236
|0 PERI:(DE-600)1491247-8
|t Journal of chromatography / A
|v 1157
|y 2007
|x 0021-9673
856 7 _ |u http://dx.doi.org/10.1016/j.chroma.2007.05.038
909 C O |o oai:juser.fz-juelich.de:57080
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|v Terrestrische Umwelt
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914 1 _ |y 2007
915 _ _ |0 StatID:(DE-HGF)0010
|a JCR/ISI refereed
920 1 _ |k ICG-3
|l Phytosphäre
|d 31.10.2010
|g ICG
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980 _ _ |a UNRESTRICTED
981 _ _ |a I:(DE-Juel1)IBG-2-20101118
981 _ _ |a I:(DE-Juel1)ICG-3-20090406


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