Publication: Free energy contribution to gas chromatographic separation of petroselinate and oleate esters
dc.contributor.author | Sansa-ard, C | en |
dc.contributor.author | Aryusuk,K | en |
dc.contributor.author | Lilitchan, S | en |
dc.contributor.author | Supathra Lilitchan | en |
dc.contributor.author | Krisnangkura, K | en |
dc.contributor.author | สุภัทรา ลิลิตชาญ | en |
dc.date.accessioned | 2011-02-10T02:58:58Z | en |
dc.date.accessioned | 2011-08-26T08:26:00Z | |
dc.date.accessioned | 2017-06-27T02:56:04Z | |
dc.date.available | 2011-02-10T02:58:58Z | en |
dc.date.available | 2011-08-26T08:26:00Z | |
dc.date.available | 2017-06-27T02:56:04Z | |
dc.date.created | 2011-02-10 | en |
dc.date.issued | 2011 | en |
dc.description.abstract | The ease of separation by gas chromatography between petroselinic and oleic acids depends on the alcoholmoieties of their esters. The esters of higher molecular weight alcohols tend to be better separated on a 90%-biscyanopropyl-10%-cyanopropylphenyl polysiloxane capillary column (30m? 0.25mmi.d.). By analysis of free energies contribution fromdifferent parts of themolecules, it is tentatively concluded that the interaction between the double bond and the column stationary phase is interfered by the bulky alkyl group, and it is the major driving force for the separation of the two fatty acids. | en |
dc.format.extent | 729845 bytes | en |
dc.format.mimetype | application/pdf | en |
dc.identifier.citation | Chromatography Research International. 2011, ID 252543 | |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/123456789/2317 | |
dc.language.iso | eng | en |
dc.rights | Mahidol University | en |
dc.source | Chromatography Research International 2011:1-9 | en |
dc.subject | Petroselinate | en |
dc.subject | Oleate Esters | en |
dc.subject | Open Access article | en_US |
dc.title | Free energy contribution to gas chromatographic separation of petroselinate and oleate esters | en |
dc.type | Article | en |
dspace.entity.type | Publication |