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Adsorption behaviou...
Adsorption behaviour of a quinidine carbamate-based chiral stationary phase : Role of the additive
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Arnell, Robert (författare)
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- Forssén, Patrik (författare)
- Uppsala universitet,Institutionen för fysikalisk och analytisk kemi
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- Fornstedt, Torgny (författare)
- Uppsala universitet,Institutionen för fysikalisk och analytisk kemi
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Sardella, Roccaldo (författare)
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Laemmerhofer, Michael (författare)
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Lindner, Wolfgang (författare)
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(creator_code:org_t)
- Elsevier BV, 2009
- 2009
- Engelska.
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Ingår i: Journal of Chromatography A. - : Elsevier BV. - 0021-9673 .- 1873-3778. ; 1216:16, s. 3480-3487
- Relaterad länk:
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https://urn.kb.se/re...
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https://doi.org/10.1...
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Abstract
Ämnesord
Stäng
- In this study, we incorporate the additive properties into the theoretical model of a general preparative chromatographic system; this is normally not done and this limits a proper process optimization. As a model phase system, we used the adsorption of 9H-fluoren-9-ylmethoxycarbonyl-allylglycine (Fmoc-allylglycine) enantiomers on a quinidine carbamate-based chiral stationary phase (anion exchanger) together with a methanol-glacial acetic acid-ammonium acetate eluent. The inverse method was used to measure the competitive adsorption isotherms of both the Fmoc-allylglycine enantiomers as well as the non-detectable additive acetic acid. It was concluded that this enantioselective preparative system is well described by a non-heterogeneous adsorption model and that the loading capacity is very high. The proposed model is valid over a wide range of additive concentrations, which is important for process optimization.
Ämnesord
- NATURVETENSKAP -- Kemi (hsv//swe)
- NATURAL SCIENCES -- Chemical Sciences (hsv//eng)
Nyckelord
- Chiral stationary phase
- Quinidine carbamate-based chiral stationary phase
- Chiral preparative chromatography
- Adsorption isotherm data
- Inverse method
- Loadability
- Chemistry
- Kemi
Publikations- och innehållstyp
- ref (ämneskategori)
- art (ämneskategori)
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