001     51790
005     20180211183649.0
024 7 _ |2 pmid
|a pmid:16545826
024 7 _ |2 DOI
|a 10.1016/j.chroma.2006.03.004
024 7 _ |2 WOS
|a WOS:000237680300036
037 _ _ |a PreJuSER-51790
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 Separation of nonylphenol ethoxylates and nonylphenol by non-aqueous capillary electrophoresis
260 _ _ |a New York, NY [u.a.]
|b Science Direct
|c 2006
300 _ _ |a 277 - 285
336 7 _ |a Journal Article
|0 PUB:(DE-HGF)16
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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 1116
500 _ _ |a Record converted from VDB: 12.11.2012
520 _ _ |a Capillary electrophoresis based on non-aqueous solvent background electrolytes was employed, with single and multiple wavelength UV detection, to evaluate discrimination among oligomer components of mixtures of non-ionic, long chain nonylphenol ethoxylates (NPnEO, with n = number of ethoxy units) and their lipophilic degradation products. The tested organic solvents included acetonitrile, methanol, ethanol, 1- and 2-propanol, 1-butanol and tetrahydrofurane in the presence of sodium acetate. A rational variation of composition of background electrolyte solvent mixtures allowed to modify the mobility of electroosmotic flow and the type and degree of interactions between the ionic additive (sodium acetate) and the components of the analyte mixtures. The physicochemical properties of the solvents, such as dielectric constant, viscosity and electron donor-acceptor ability regarding the additive, were considered to improve the resolution of lipophilic compounds with less than three ethoxy groups and the discrimination attainable for longer chain oligomers. The studied methodologies also allowed discerning between surfactants of similar (nominal) ethoxy chain lengths. This was demonstrated by the different peak distribution patterns observed for NPnEO compounds with n = 7.5 and 10, respectively.
536 _ _ |a Terrestrische Umwelt
|c P24
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588 _ _ |a Dataset connected to Web of Science, Pubmed
650 _ 2 |2 MeSH
|a Electrophoresis, Capillary: methods
650 _ 2 |2 MeSH
|a Ethylene Glycols: isolation & purification
650 _ 2 |2 MeSH
|a Phenols: isolation & purification
650 _ 2 |2 MeSH
|a Spectrophotometry, Ultraviolet
650 _ 2 |2 MeSH
|a Surface-Active Agents: isolation & purification
650 _ 2 |2 MeSH
|a Viscosity
650 _ 7 |0 0
|2 NLM Chemicals
|a Ethylene Glycols
650 _ 7 |0 0
|2 NLM Chemicals
|a Phenols
650 _ 7 |0 0
|2 NLM Chemicals
|a Surface-Active Agents
650 _ 7 |0 25154-52-3
|2 NLM Chemicals
|a nonylphenol
650 _ 7 |0 27986-36-3
|2 NLM Chemicals
|a terics
650 _ 7 |a J
|2 WoSType
653 2 0 |2 Author
|a non-aqueous capillary electrophoresis
653 2 0 |2 Author
|a nonylphenol ethoxylates
653 2 0 |2 Author
|a lipophilic metabolites
653 2 0 |2 Author
|a cationic complexes
653 2 0 |2 Author
|a heteroconjugation
700 1 _ |a Gettar, R. T.
|b 1
|0 P:(DE-HGF)0
700 1 _ |a Silva, M. F.
|b 2
|0 P:(DE-HGF)0
700 1 _ |a Thiele, B.
|b 3
|u FZJ
|0 P:(DE-Juel1)129410
700 1 _ |a Batistoni, D. A.
|b 4
|0 P:(DE-HGF)0
773 _ _ |a 10.1016/j.chroma.2006.03.004
|g Vol. 1116, p. 277 - 285
|p 277 - 285
|q 1116<277 - 285
|0 PERI:(DE-600)1491247-8
|t Journal of chromatography / A
|v 1116
|y 2006
|x 0021-9673
856 7 _ |u http://dx.doi.org/10.1016/j.chroma.2006.03.004
909 C O |o oai:juser.fz-juelich.de:51790
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913 1 _ |k P24
|v Terrestrische Umwelt
|l Terrestrische Umwelt
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914 1 _ |y 2006
915 _ _ |0 StatID:(DE-HGF)0010
|a JCR/ISI refereed
920 1 _ |k ICG-III
|l Phytosphäre
|d 31.12.2006
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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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