PL150101B1 - Method of obtaining isomerized vegetable oil - Google Patents
Method of obtaining isomerized vegetable oilInfo
- Publication number
- PL150101B1 PL150101B1 PL26690487A PL26690487A PL150101B1 PL 150101 B1 PL150101 B1 PL 150101B1 PL 26690487 A PL26690487 A PL 26690487A PL 26690487 A PL26690487 A PL 26690487A PL 150101 B1 PL150101 B1 PL 150101B1
- Authority
- PL
- Poland
- Prior art keywords
- oil
- catalyst
- vegetable oil
- reaction medium
- isomerization
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 25
- 235000015112 vegetable and seed oil Nutrition 0.000 title claims description 6
- 239000008158 vegetable oil Substances 0.000 title claims description 6
- 239000003054 catalyst Substances 0.000 claims description 15
- 239000003921 oil Substances 0.000 claims description 14
- 235000019198 oils Nutrition 0.000 claims description 13
- 238000006317 isomerization reaction Methods 0.000 claims description 11
- 239000000010 aprotic solvent Substances 0.000 claims description 7
- 239000012429 reaction media Substances 0.000 claims description 7
- 150000004703 alkoxides Chemical class 0.000 claims description 6
- 239000000725 suspension Substances 0.000 claims description 6
- 239000011261 inert gas Substances 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 238000002604 ultrasonography Methods 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims 1
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
- BDAWXSQJJCIFIK-UHFFFAOYSA-N potassium methoxide Chemical compound [K+].[O-]C BDAWXSQJJCIFIK-UHFFFAOYSA-N 0.000 description 5
- 238000007086 side reaction Methods 0.000 description 5
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 235000019484 Rapeseed oil Nutrition 0.000 description 3
- 239000003973 paint Substances 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- 239000002966 varnish Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 230000021615 conjugation Effects 0.000 description 2
- 238000006073 displacement reaction Methods 0.000 description 2
- 230000003628 erosive effect Effects 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000013467 fragmentation Methods 0.000 description 1
- 238000006062 fragmentation reaction Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 238000009210 therapy by ultrasound Methods 0.000 description 1
- -1 unsaturated fatty acid esters Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL26690487A PL150101B1 (en) | 1987-07-16 | 1987-07-16 | Method of obtaining isomerized vegetable oil |
| CS885082A CS508288A3 (en) | 1987-07-16 | 1988-07-14 | Process for preparing vegetable oil modified by isomerization |
| SU884356186A SU1679976A3 (ru) | 1987-07-16 | 1988-07-15 | Способ получени изомеризованного растительного масла |
| DD31799088A DD281814A5 (de) | 1987-07-16 | 1988-07-15 | Verfahren zur herstellung von isomerisiertem pflanzlichem oel |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL26690487A PL150101B1 (en) | 1987-07-16 | 1987-07-16 | Method of obtaining isomerized vegetable oil |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| PL266904A1 PL266904A1 (en) | 1989-01-23 |
| PL150101B1 true PL150101B1 (en) | 1990-04-30 |
Family
ID=20037391
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL26690487A PL150101B1 (en) | 1987-07-16 | 1987-07-16 | Method of obtaining isomerized vegetable oil |
Country Status (2)
| Country | Link |
|---|---|
| DD (1) | DD281814A5 (de) |
| PL (1) | PL150101B1 (de) |
-
1987
- 1987-07-16 PL PL26690487A patent/PL150101B1/pl unknown
-
1988
- 1988-07-15 DD DD31799088A patent/DD281814A5/de not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| PL266904A1 (en) | 1989-01-23 |
| DD281814A5 (de) | 1990-08-22 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Roschat et al. | Synthesis of glycerol carbonate from transesterification of glycerol with dimethyl carbonate catalyzed by CaO from natural sources as green and economical catalyst | |
| JP2003512507A (ja) | 加アルコール分解による生物由来の脂肪および/又は油のエステル交換方法 | |
| Mazo et al. | Self-esterification of partially maleated castor oil using conventional and microwave heating | |
| JPH05500505A (ja) | 低級アルキルエステルの連続製造方法 | |
| Amalia et al. | Biodiesel production from castor oil using heterogeneous catalyst KOH/zeolite of natural zeolite Bandung Indonesia | |
| CN109400811A (zh) | 离子液体中合成蔗渣木聚糖乙酰苯丙氨酸酯-g-CHMA的方法 | |
| MX2010011628A (es) | Preparacion de fluoruro de hidrogeno a partir de material residual que contiene fluorita o fluoruro de calcio. | |
| PL150101B1 (en) | Method of obtaining isomerized vegetable oil | |
| PL150102B1 (pl) | Sposób wytwarzania izomeryzowanego oleju roślinnego | |
| Gite et al. | Synthesis of n-octyl acetate using heterogeneous catalyst: kinetic and thermodynamic study | |
| NO180714B (no) | Fremgangsmåte til fremstilling av oksamid | |
| PL150086B1 (en) | Method of obtaining an isomerized vegetable oil | |
| EP4482897A1 (de) | (poly)ester- und (poly)amidzusammensetzungen, verfahren zur modifizierung von (poly)estern oder (poly)amiden und katalysator dafür | |
| RU2359956C1 (ru) | Способ получения оксалата марганца (ii) | |
| EP0281266A1 (de) | 3-Amino-2,4,5-trifluorobenzoesäure und ihre Herstellung | |
| Al-Mulla et al. | Enzymatic synthesis of palm olein-based fatty thiohydroxamic acids | |
| Sharma et al. | Fly ash supported perchloric acid (PAFA): a green, highly efficient and recyclable heterogeneous catalyst for series of esterification | |
| RU2126789C1 (ru) | Способ получения n,n'- дифенил-n-фенилендиамина | |
| Haoue et al. | A New Green Catalyst for Synthesis of bis-Macromonomers of Polyethylene Glycol (PEG) | |
| SU1395646A1 (ru) | Способ получени аммонийной соли тетрасульфофталоцианиновых металлокомплексов | |
| JPH0873397A (ja) | 金属石鹸の製造方法 | |
| SU939526A1 (ru) | Способ получени депрессорной присадки к нефтепродуктам | |
| NL8302367A (nl) | Katalytische bereiding van carbonamiden. | |
| JP3546462B2 (ja) | ポリグリセリン脂肪酸エステルの分離方法 | |
| PL229108B1 (pl) | Sposób wydzielania i oczyszczania estrów chityny (mono-, di‑podstawionych) oraz kopoliestrów chityny z mieszanin poreakcyjnych |