Selective conjugation of soybean esters to increase hydrogenation selectivity
Abstract Polyunsaturated fatty acid methyl esters of soybean oil (MeSBO) were selectively conjugated as a means of increasing the linolenate selectivity of various homogeneous and heterogeneous hydrogenation catalysts. Kinetics of the conjugation reaction in various solvents indicated that linolenat...
Ausführliche Beschreibung
Autor*in: |
Koritala, S. [verfasserIn] |
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Format: |
Artikel |
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Sprache: |
Englisch |
Erschienen: |
1981 |
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Anmerkung: |
© American Oil Chemists’ Society 1981 |
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Übergeordnetes Werk: |
Enthalten in: Journal of the American Oil Chemists Society - Springer-Verlag, 1947, 58(1981), 4 vom: Apr., Seite 553-556 |
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Übergeordnetes Werk: |
volume:58 ; year:1981 ; number:4 ; month:04 ; pages:553-556 |
Links: |
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DOI / URN: |
10.1007/BF02541593 |
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Katalog-ID: |
OLC2068079720 |
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520 | |a Abstract Polyunsaturated fatty acid methyl esters of soybean oil (MeSBO) were selectively conjugated as a means of increasing the linolenate selectivity of various homogeneous and heterogeneous hydrogenation catalysts. Kinetics of the conjugation reaction in various solvents indicated that linolenate conjugated 5–8 times faster than linoleate. Selective conjugation of MeSBO with potassiumt-butoxide in dipolar solvents resulted in an increase in linolenate hydrogenation selectivity to 7–8 with Ni and Pd heterogeneous catalysts, and to 7–10 with homogeneous and heterogeneous chromium carbonyl catalysts.Trans-unsaturation in the hydrogenated products was only 1–3% with the chromium carbonyl catalysts, in contrast to 30–39% with the heterogeneous metal catalysts. Triglycerides were readily converted to partial glycerides andt-butyl esters with the potassiumt-butoxide reagent. | ||
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10.1007/BF02541593 doi (DE-627)OLC2068079720 (DE-He213)BF02541593-p DE-627 ger DE-627 rakwb eng 660 VZ Koritala, S. verfasserin aut Selective conjugation of soybean esters to increase hydrogenation selectivity 1981 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © American Oil Chemists’ Society 1981 Abstract Polyunsaturated fatty acid methyl esters of soybean oil (MeSBO) were selectively conjugated as a means of increasing the linolenate selectivity of various homogeneous and heterogeneous hydrogenation catalysts. Kinetics of the conjugation reaction in various solvents indicated that linolenate conjugated 5–8 times faster than linoleate. Selective conjugation of MeSBO with potassiumt-butoxide in dipolar solvents resulted in an increase in linolenate hydrogenation selectivity to 7–8 with Ni and Pd heterogeneous catalysts, and to 7–10 with homogeneous and heterogeneous chromium carbonyl catalysts.Trans-unsaturation in the hydrogenated products was only 1–3% with the chromium carbonyl catalysts, in contrast to 30–39% with the heterogeneous metal catalysts. Triglycerides were readily converted to partial glycerides andt-butyl esters with the potassiumt-butoxide reagent. Linolenate Methyl Linolenate Diglyme Conjugate Triene Tetraglyme Frankel, E. N. aut Enthalten in Journal of the American Oil Chemists Society Springer-Verlag, 1947 58(1981), 4 vom: Apr., Seite 553-556 (DE-627)129595691 (DE-600)240684-6 (DE-576)015088715 0003-021X nnns volume:58 year:1981 number:4 month:04 pages:553-556 https://doi.org/10.1007/BF02541593 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_26 GBV_ILN_40 GBV_ILN_70 GBV_ILN_95 GBV_ILN_2360 GBV_ILN_4012 GBV_ILN_4036 GBV_ILN_4046 GBV_ILN_4125 GBV_ILN_4219 GBV_ILN_4306 GBV_ILN_4315 AR 58 1981 4 04 553-556 |
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10.1007/BF02541593 doi (DE-627)OLC2068079720 (DE-He213)BF02541593-p DE-627 ger DE-627 rakwb eng 660 VZ Koritala, S. verfasserin aut Selective conjugation of soybean esters to increase hydrogenation selectivity 1981 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © American Oil Chemists’ Society 1981 Abstract Polyunsaturated fatty acid methyl esters of soybean oil (MeSBO) were selectively conjugated as a means of increasing the linolenate selectivity of various homogeneous and heterogeneous hydrogenation catalysts. Kinetics of the conjugation reaction in various solvents indicated that linolenate conjugated 5–8 times faster than linoleate. Selective conjugation of MeSBO with potassiumt-butoxide in dipolar solvents resulted in an increase in linolenate hydrogenation selectivity to 7–8 with Ni and Pd heterogeneous catalysts, and to 7–10 with homogeneous and heterogeneous chromium carbonyl catalysts.Trans-unsaturation in the hydrogenated products was only 1–3% with the chromium carbonyl catalysts, in contrast to 30–39% with the heterogeneous metal catalysts. Triglycerides were readily converted to partial glycerides andt-butyl esters with the potassiumt-butoxide reagent. Linolenate Methyl Linolenate Diglyme Conjugate Triene Tetraglyme Frankel, E. N. aut Enthalten in Journal of the American Oil Chemists Society Springer-Verlag, 1947 58(1981), 4 vom: Apr., Seite 553-556 (DE-627)129595691 (DE-600)240684-6 (DE-576)015088715 0003-021X nnns volume:58 year:1981 number:4 month:04 pages:553-556 https://doi.org/10.1007/BF02541593 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_26 GBV_ILN_40 GBV_ILN_70 GBV_ILN_95 GBV_ILN_2360 GBV_ILN_4012 GBV_ILN_4036 GBV_ILN_4046 GBV_ILN_4125 GBV_ILN_4219 GBV_ILN_4306 GBV_ILN_4315 AR 58 1981 4 04 553-556 |
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10.1007/BF02541593 doi (DE-627)OLC2068079720 (DE-He213)BF02541593-p DE-627 ger DE-627 rakwb eng 660 VZ Koritala, S. verfasserin aut Selective conjugation of soybean esters to increase hydrogenation selectivity 1981 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © American Oil Chemists’ Society 1981 Abstract Polyunsaturated fatty acid methyl esters of soybean oil (MeSBO) were selectively conjugated as a means of increasing the linolenate selectivity of various homogeneous and heterogeneous hydrogenation catalysts. Kinetics of the conjugation reaction in various solvents indicated that linolenate conjugated 5–8 times faster than linoleate. Selective conjugation of MeSBO with potassiumt-butoxide in dipolar solvents resulted in an increase in linolenate hydrogenation selectivity to 7–8 with Ni and Pd heterogeneous catalysts, and to 7–10 with homogeneous and heterogeneous chromium carbonyl catalysts.Trans-unsaturation in the hydrogenated products was only 1–3% with the chromium carbonyl catalysts, in contrast to 30–39% with the heterogeneous metal catalysts. Triglycerides were readily converted to partial glycerides andt-butyl esters with the potassiumt-butoxide reagent. Linolenate Methyl Linolenate Diglyme Conjugate Triene Tetraglyme Frankel, E. N. aut Enthalten in Journal of the American Oil Chemists Society Springer-Verlag, 1947 58(1981), 4 vom: Apr., Seite 553-556 (DE-627)129595691 (DE-600)240684-6 (DE-576)015088715 0003-021X nnns volume:58 year:1981 number:4 month:04 pages:553-556 https://doi.org/10.1007/BF02541593 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_26 GBV_ILN_40 GBV_ILN_70 GBV_ILN_95 GBV_ILN_2360 GBV_ILN_4012 GBV_ILN_4036 GBV_ILN_4046 GBV_ILN_4125 GBV_ILN_4219 GBV_ILN_4306 GBV_ILN_4315 AR 58 1981 4 04 553-556 |
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10.1007/BF02541593 doi (DE-627)OLC2068079720 (DE-He213)BF02541593-p DE-627 ger DE-627 rakwb eng 660 VZ Koritala, S. verfasserin aut Selective conjugation of soybean esters to increase hydrogenation selectivity 1981 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © American Oil Chemists’ Society 1981 Abstract Polyunsaturated fatty acid methyl esters of soybean oil (MeSBO) were selectively conjugated as a means of increasing the linolenate selectivity of various homogeneous and heterogeneous hydrogenation catalysts. Kinetics of the conjugation reaction in various solvents indicated that linolenate conjugated 5–8 times faster than linoleate. Selective conjugation of MeSBO with potassiumt-butoxide in dipolar solvents resulted in an increase in linolenate hydrogenation selectivity to 7–8 with Ni and Pd heterogeneous catalysts, and to 7–10 with homogeneous and heterogeneous chromium carbonyl catalysts.Trans-unsaturation in the hydrogenated products was only 1–3% with the chromium carbonyl catalysts, in contrast to 30–39% with the heterogeneous metal catalysts. Triglycerides were readily converted to partial glycerides andt-butyl esters with the potassiumt-butoxide reagent. Linolenate Methyl Linolenate Diglyme Conjugate Triene Tetraglyme Frankel, E. N. aut Enthalten in Journal of the American Oil Chemists Society Springer-Verlag, 1947 58(1981), 4 vom: Apr., Seite 553-556 (DE-627)129595691 (DE-600)240684-6 (DE-576)015088715 0003-021X nnns volume:58 year:1981 number:4 month:04 pages:553-556 https://doi.org/10.1007/BF02541593 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_26 GBV_ILN_40 GBV_ILN_70 GBV_ILN_95 GBV_ILN_2360 GBV_ILN_4012 GBV_ILN_4036 GBV_ILN_4046 GBV_ILN_4125 GBV_ILN_4219 GBV_ILN_4306 GBV_ILN_4315 AR 58 1981 4 04 553-556 |
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10.1007/BF02541593 doi (DE-627)OLC2068079720 (DE-He213)BF02541593-p DE-627 ger DE-627 rakwb eng 660 VZ Koritala, S. verfasserin aut Selective conjugation of soybean esters to increase hydrogenation selectivity 1981 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © American Oil Chemists’ Society 1981 Abstract Polyunsaturated fatty acid methyl esters of soybean oil (MeSBO) were selectively conjugated as a means of increasing the linolenate selectivity of various homogeneous and heterogeneous hydrogenation catalysts. Kinetics of the conjugation reaction in various solvents indicated that linolenate conjugated 5–8 times faster than linoleate. Selective conjugation of MeSBO with potassiumt-butoxide in dipolar solvents resulted in an increase in linolenate hydrogenation selectivity to 7–8 with Ni and Pd heterogeneous catalysts, and to 7–10 with homogeneous and heterogeneous chromium carbonyl catalysts.Trans-unsaturation in the hydrogenated products was only 1–3% with the chromium carbonyl catalysts, in contrast to 30–39% with the heterogeneous metal catalysts. Triglycerides were readily converted to partial glycerides andt-butyl esters with the potassiumt-butoxide reagent. Linolenate Methyl Linolenate Diglyme Conjugate Triene Tetraglyme Frankel, E. N. aut Enthalten in Journal of the American Oil Chemists Society Springer-Verlag, 1947 58(1981), 4 vom: Apr., Seite 553-556 (DE-627)129595691 (DE-600)240684-6 (DE-576)015088715 0003-021X nnns volume:58 year:1981 number:4 month:04 pages:553-556 https://doi.org/10.1007/BF02541593 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_26 GBV_ILN_40 GBV_ILN_70 GBV_ILN_95 GBV_ILN_2360 GBV_ILN_4012 GBV_ILN_4036 GBV_ILN_4046 GBV_ILN_4125 GBV_ILN_4219 GBV_ILN_4306 GBV_ILN_4315 AR 58 1981 4 04 553-556 |
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selective conjugation of soybean esters to increase hydrogenation selectivity |
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Selective conjugation of soybean esters to increase hydrogenation selectivity |
abstract |
Abstract Polyunsaturated fatty acid methyl esters of soybean oil (MeSBO) were selectively conjugated as a means of increasing the linolenate selectivity of various homogeneous and heterogeneous hydrogenation catalysts. Kinetics of the conjugation reaction in various solvents indicated that linolenate conjugated 5–8 times faster than linoleate. Selective conjugation of MeSBO with potassiumt-butoxide in dipolar solvents resulted in an increase in linolenate hydrogenation selectivity to 7–8 with Ni and Pd heterogeneous catalysts, and to 7–10 with homogeneous and heterogeneous chromium carbonyl catalysts.Trans-unsaturation in the hydrogenated products was only 1–3% with the chromium carbonyl catalysts, in contrast to 30–39% with the heterogeneous metal catalysts. Triglycerides were readily converted to partial glycerides andt-butyl esters with the potassiumt-butoxide reagent. © American Oil Chemists’ Society 1981 |
abstractGer |
Abstract Polyunsaturated fatty acid methyl esters of soybean oil (MeSBO) were selectively conjugated as a means of increasing the linolenate selectivity of various homogeneous and heterogeneous hydrogenation catalysts. Kinetics of the conjugation reaction in various solvents indicated that linolenate conjugated 5–8 times faster than linoleate. Selective conjugation of MeSBO with potassiumt-butoxide in dipolar solvents resulted in an increase in linolenate hydrogenation selectivity to 7–8 with Ni and Pd heterogeneous catalysts, and to 7–10 with homogeneous and heterogeneous chromium carbonyl catalysts.Trans-unsaturation in the hydrogenated products was only 1–3% with the chromium carbonyl catalysts, in contrast to 30–39% with the heterogeneous metal catalysts. Triglycerides were readily converted to partial glycerides andt-butyl esters with the potassiumt-butoxide reagent. © American Oil Chemists’ Society 1981 |
abstract_unstemmed |
Abstract Polyunsaturated fatty acid methyl esters of soybean oil (MeSBO) were selectively conjugated as a means of increasing the linolenate selectivity of various homogeneous and heterogeneous hydrogenation catalysts. Kinetics of the conjugation reaction in various solvents indicated that linolenate conjugated 5–8 times faster than linoleate. Selective conjugation of MeSBO with potassiumt-butoxide in dipolar solvents resulted in an increase in linolenate hydrogenation selectivity to 7–8 with Ni and Pd heterogeneous catalysts, and to 7–10 with homogeneous and heterogeneous chromium carbonyl catalysts.Trans-unsaturation in the hydrogenated products was only 1–3% with the chromium carbonyl catalysts, in contrast to 30–39% with the heterogeneous metal catalysts. Triglycerides were readily converted to partial glycerides andt-butyl esters with the potassiumt-butoxide reagent. © American Oil Chemists’ Society 1981 |
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container_issue |
4 |
title_short |
Selective conjugation of soybean esters to increase hydrogenation selectivity |
url |
https://doi.org/10.1007/BF02541593 |
remote_bool |
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author2 |
Frankel, E. N. |
author2Str |
Frankel, E. N. |
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doi_str |
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up_date |
2024-07-03T17:31:40.880Z |
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