SE417441B - PROCEDURE FOR INSULATING POLERA LIPIDES FROM A MIXTURE OF POLERA AND OPOLERA CEREALICLIPIDES BY MIXING WITH THE WATER AND THEIR FOLLOWING Gravity Separation - Google Patents
PROCEDURE FOR INSULATING POLERA LIPIDES FROM A MIXTURE OF POLERA AND OPOLERA CEREALICLIPIDES BY MIXING WITH THE WATER AND THEIR FOLLOWING Gravity SeparationInfo
- Publication number
- SE417441B SE417441B SE7709374A SE7709374A SE417441B SE 417441 B SE417441 B SE 417441B SE 7709374 A SE7709374 A SE 7709374A SE 7709374 A SE7709374 A SE 7709374A SE 417441 B SE417441 B SE 417441B
- Authority
- SE
- Sweden
- Prior art keywords
- water
- mixture
- polera
- gravity separation
- opolera
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B7/00—Separation of mixtures of fats or fatty oils into their constituents, e.g. saturated oils from unsaturated oils
-
- A—HUMAN NECESSITIES
- A21—BAKING; EDIBLE DOUGHS
- A21D—TREATMENT, e.g. PRESERVATION, OF FLOUR OR DOUGH, e.g. BY ADDITION OF MATERIALS; BAKING; BAKERY PRODUCTS; PRESERVATION THEREOF
- A21D2/00—Treatment of flour or dough by adding materials thereto before or during baking
- A21D2/08—Treatment of flour or dough by adding materials thereto before or during baking by adding organic substances
- A21D2/14—Organic oxygen compounds
- A21D2/16—Fatty acid esters
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Food Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Bakery Products And Manufacturing Methods Therefor (AREA)
- Compounds Of Unknown Constitution (AREA)
- Fats And Perfumes (AREA)
- Cereal-Derived Products (AREA)
Description
7109:74-s t.ex. stearyl-laktyl-laktat-salter, vinsyreestrar och monoglycerider. 7109: 74-s e.g. stearyl-lactyl-lactate salts, tartaric acid esters and monoglycerides.
De ger brödet en förbättrad spannmålsarom, en ökad volym, samt förbättrad textur och hållbarhet. De polära cerealielipidernas goda effekt vid bakning är tidigare känd från t.ex. Mac Ritchie: 5 J. Scí. FD Agric.,g§(l977), 53-58. Andra användningar är som till- sats till stärkelsebaserade livsmedel såsom pastor, potatismos, välling, där produkten ger lívsmedlet en kortare textur. Upp- finningen avser avlägsnande av opolära lipider ur totalextraktet, eftersom dessa motverkar de önskade effekterna hos nämnda produkt- 10 typer. Det är därför önskvärt att isoleringen av de polära lipiderna blir så effektiv att dessa kommer att innehålla högst 25 viktsprocent opolära lipider.They give the bread an improved grain aroma, an increased volume, as well as improved texture and durability. The good effect of the polar cereal lipids in baking is previously known from e.g. Mac Ritchie: 5 J. Scí. FD Agric., G§ (l977), 53-58. Other uses are as an additive to starch-based foods such as pasta, mashed potatoes, gruel, where the product gives the food a shorter texture. The invention relates to the removal of non-polar lipids from the total extract, since these counteract the desired effects of said product types. It is therefore desirable that the isolation of the polar lipids be so effective that they will contain at most 25% by weight of non-polar lipids.
Förfarandet enligt uppfinningen kännetecknas därav, att man blandar lipidblandningen med vatten i en sådan mängd att l5 lipid-vatten-blandningen innehåller minst 50 viktsprocent vatten, varefter man utsätter blandningen för en tyngdkraftseparation, och att man slutligen tillvaratager den vid tyngdkraftseparationen bildade tyngsta oljeliknande fasen, som innehåller huvuddelen av de polära lipiderna. 20 Lipidblandningen försättes alltså med vatten, lämpligen destillerat vatten, i en sådan mängd att lipid-vatten-blandningen innehåller minst 50 viktsprocent vatten. Vi har funnit 70 Vikts- procent vatten vara en lämplig vattenhalt. Om vattenhalten är högre än 80 viktsprocent blir blandningens volym så stor att 25 tyngdkraftseparationen bereder svårigheter. Blandningens tempera- tur bör helst hållas högre än 2500 för att den önskade fasen skall få lämplig konsistens ur hanteringssynpunkt. Temperaturen bör dock understiga 5000 för undvikande av fettoxidation. Efter 5-6 timmar har fasjämvikt uppnåtts. Blandningen underkastas nu 50 tyngdkraftseparation, lämpligen i en centrifugalseparator. Vid centrifugering vid 5000-10000 g har faserna separerat full- ständigt efter 0,5-2 timmar. Den översta, lättaste fasen är en olja som nästan helt utgörs av opolära lipider, främst triglycerider.The process according to the invention is characterized in that the lipid mixture is mixed with water in such an amount that the lipid-water mixture contains at least 50% by weight of water, after which the mixture is subjected to a gravity separation, and that finally the heaviest oil-like phase formed in gravity separation is recovered. which contains the majority of the polar lipids. The lipid mixture is thus added with water, suitably distilled water, in such an amount that the lipid-water mixture contains at least 50% by weight of water. We have found 70% by weight of water to be a suitable water content. If the water content is higher than 80% by weight, the volume of the mixture becomes so large that the gravity separation creates difficulties. The temperature of the mixture should preferably be kept higher than 2500 in order for the desired phase to have a suitable consistency from a handling point of view. However, the temperature should be below 5000 to avoid fat oxidation. After 5-6 hours, phase equilibrium has been reached. The mixture is now subjected to gravity separation, preferably in a centrifugal separator. When centrifuged at 5000-10000 g, the phases have separated completely after 0.5-2 hours. The top, lightest phase is an oil that consists almost entirely of non-polar lipids, mainly triglycerides.
Under denna fas ligger en ren vattenfas. Den understa, tyngsta 35 fasen är en svagt gulfärgad oljeliknande fas som innehåller de önskade polära lipiderna. Vi har funnit att denna fas oväntat nog fiurïåller en hög halt vatten, nämligen ca 50-70 viktsprocent, beroende av tillsatt vattenmängd. Trots detta är fasen ej blandbar med vatten.Below this phase is a pure water phase. The lowest, heaviest phase is a pale yellow oil-like phase which contains the desired polar lipids. We have found that this phase unexpectedly contains a high content of water, namely about 50-70% by weight, depending on the amount of water added. Despite this, the phase is immiscible with water.
H0 halten opolära lipider i den oljelíknande fas som inno- håller de polära lipiderna kan bringas att minska något (från högst 10 20 25 35 770937lr-8 ca 25 % till högst ca 10) om man tillsätter ett salt till det vatten varmed man tillsätter lipidextraktet. Vattnets salthalt är lämpligen 0,U-H viktsprocent. Saltet utgörs lämpligen av ett halogensalt av en alkalímetall.The content of non-polar lipids in the oil-like phase containing the polar lipids can be reduced somewhat (from a maximum of about 25% to a maximum of about 10) if a salt is added to the water with which the lipid extract is added. . The salinity of the water is suitably 0.1% by weight. The salt is suitably a halogen salt of an alkali metal.
Exemgel: Exemplet behandlar framställning av en lipidblandning ur vetemjöl, isolering av polära lipider, samt användning av de polära lipiderna vid bakning.Example gel: The example deals with the preparation of a lipid mixture from wheat flour, isolation of polar lipids, and the use of the polar lipids in baking.
A. Lipidframställning ur vetemjöl. 10 kg vetemjöl försattes i en blandare med Ä0 kg vattenmättad butanol. Blandaren kördes 2 timmar. Blandningens temperatur var 20-2500. Blandningen överfördes till en centrifugal- separator och centrifugerades vid 1800 g under en timme. Härvid erhölls ca 35 liter vätska. Denna indunstades genom uppvärmning vid 5000. Härvid erhölls en torr återstod vägande ca 160 g. Det är ur livsmedelssynpunkt viktigt att indunstningen blir fullständig, så att inget organiskt lösningsmedel återstår i lipidblandningen.A. Lipid production from wheat flour. 10 kg of wheat flour was added to a mixer with Ä0 kg of water-saturated butanol. The mixer was run for 2 hours. The temperature of the mixture was 20-2500. The mixture was transferred to a centrifugal separator and centrifuged at 1800 g for one hour. This gave about 35 liters of liquid. This was evaporated by heating at 5000. A dry residue weighing about 160 g was obtained. It is important from a food point of view that the evaporation is complete, so that no organic solvent remains in the lipid mixture.
B. Isolering av polära lipider. 500 g av en lipidblandning av det slag som framställts enligt steg A försattes med 700 g destillerat vatten och omrördes tills en till synes homogen blandning erhållits. Blandningen fick stå i 4 timmar vid 3000 utan omröring. Därefter överfördes den till en centrifugalseparator och centrifugerades vid 5000 g under l timme. Därvid erhölls två oljeliknande faser, skilda av ett vattenskikt. Den tyngsta oljeliknande fasen tillvaratogs. Den hade en volym av 750 ml och befanns innehålla 70 % vatten.B. Isolation of polar lipids. 500 g of a lipid mixture of the kind prepared according to step A were added with 700 g of distilled water and stirred until a seemingly homogeneous mixture was obtained. The mixture was allowed to stand for 4 hours at 3000 without stirring. It was then transferred to a centrifugal separator and centrifuged at 5000 g for 1 hour. Thereby, two oil-like phases were obtained, separated by a water layer. The heaviest oil-like phase was recovered. It had a volume of 750 ml and was found to contain 70% water.
C. Bakning.C. Baking.
Bakförsök utfördes på standardiserat sätt enligt metodik från Utsädesföreningen i Svalöv. Vetemjölet var s.k. bageriblandníng från Kungsörnen. Jässkåp och ugn av fabrikat Simons (England) an- vändes. De polära vetelipiderna enligt steg B tillsattes i en mängd av 0,83 viktsprocent av mjölmängden. Som jämförelse bakades dels bröd med en lika stor tillsats av natriumstearyl-laktyl-laktat, samt bröd utan någon extra emulgatortillsats. Följande resultat erhölls. Porositeten anges i en skala l-8, där högsta siffran anger fin porositet. Inkråmets elasticitet anges i en skala l-6, där 6 anger en mycket god elasticitet. Brödutseendet anges i en skala l-H, där l är det bästa värdet och anger ett felfritt utseende. 77093711-8 i! Tid till § Bröd- Inkråm Bröd- oaccepta- Bröd volym Porosí- elasti- utseende bel hård- ml tet citet het * dygn :Ingen tillsats , Iuo É 6 14 1 in Natriumstearyl- i ä -lalgfiyl-dlaktat ; g i 0,85 % På mjöl- 2 f Å mängd É H80 § 6 2 l g 4 4 :_ Polära Vetelipiderß 2 ¿ enl. uppfinningen ¿ f É .,, l f f 0,83 % på mJo1- , ' § mängd § H90 g 6 6 l É 6 ¿ I aDessutom noterades att texturen hos inkråm och smak på det bakade brödet var överlägset bäst för den baksats som innehöll de polära vetelipiderna. Det är välkänt att emulgatortillsats ger smulighet hos brödet, vilket var mycket tydligt i vårt jämförelseförsök.Baking experiments were performed in a standardized manner according to methodology from the Seed Association in Svalöv. The wheat flour was so-called bakery mix from Kungsörnen. Fermenters and ovens made by Simons (England) were used. The polar wheat lipids of step B were added in an amount of 0.83% by weight of the amount of flour. For comparison, bread was baked with an equal addition of sodium stearyl-lactyl-lactate, and bread without any additional emulsifier additive. The following results were obtained. The porosity is given on a scale of 1-8, where the highest number indicates fine porosity. The elasticity of the crust is indicated on a scale of 1-6, where 6 indicates a very good elasticity. The bread appearance is given in a scale l-H, where l is the best value and indicates a flawless appearance. 77093711-8 i! Time to § Bread- Ingredients Bread- unaccept- Bread volume Porosí- elasti- appearance bel hard- ml tet citet hot * day: No additive, Iuo É 6 14 1 in Sodium stearyl- i ä -lalg fi yl-lactate; g in 0.85% On flour- 2 f Å amount É H80 § 6 2 l g 4 4: _ Polar Wheat Lipidsß 2 ¿acc. invention ¿f É. ,, lff 0.83% on mJo1-, '§ quantity § H90 g 6 6 l É 6 ¿I aIn addition, it was noted that the texture of the ingredients and taste of the baked bread was by far the best for the baking that contained the the polar wheat lipids. It is well known that emulsifier additive gives crumb to the bread, which was very clear in our comparison experiment.
De polära vetelipiderna ger inga sådana effekter.The polar wheat lipids do not produce such effects.
Claims (1)
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE7709374A SE417441B (en) | 1977-08-19 | 1977-08-19 | PROCEDURE FOR INSULATING POLERA LIPIDES FROM A MIXTURE OF POLERA AND OPOLERA CEREALICLIPIDES BY MIXING WITH THE WATER AND THEIR FOLLOWING Gravity Separation |
AU38631/78A AU522378B2 (en) | 1977-08-19 | 1978-08-04 | Polar lipids |
DE19782834999 DE2834999A1 (en) | 1977-08-19 | 1978-08-10 | PROCESS FOR THE ISOLATION OF POLAR LIPIDS FROM A MIXTURE OF POLAR AND NON-POLAR GRAIN LIPIDS |
CA309,300A CA1102795A (en) | 1977-08-19 | 1978-08-14 | Method of isolating polar lipids from a mixture of polar and non-polar cereal lipids |
FI782477A FI782477A (en) | 1977-08-19 | 1978-08-14 | FOERFARANDE FOER ATT ISOLERA POLAERA LIPIDER UR EN BLANDNING AV POLAERA OCH OPOLAERA CEREALIELIPIDER |
FR7824047A FR2400552A1 (en) | 1977-08-19 | 1978-08-17 | Sepg. polar lipid(s) from non-polar lipid(s) for use as food additives - by mixing with water a lipid mixt. extracted from cereals, and centrifuging |
JP10136578A JPS5452003A (en) | 1977-08-19 | 1978-08-18 | Method of isolating polar lipid from grain lipid mixture |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE7709374A SE417441B (en) | 1977-08-19 | 1977-08-19 | PROCEDURE FOR INSULATING POLERA LIPIDES FROM A MIXTURE OF POLERA AND OPOLERA CEREALICLIPIDES BY MIXING WITH THE WATER AND THEIR FOLLOWING Gravity Separation |
Publications (2)
Publication Number | Publication Date |
---|---|
SE7709374L SE7709374L (en) | 1979-02-20 |
SE417441B true SE417441B (en) | 1981-03-16 |
Family
ID=20332052
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SE7709374A SE417441B (en) | 1977-08-19 | 1977-08-19 | PROCEDURE FOR INSULATING POLERA LIPIDES FROM A MIXTURE OF POLERA AND OPOLERA CEREALICLIPIDES BY MIXING WITH THE WATER AND THEIR FOLLOWING Gravity Separation |
Country Status (7)
Country | Link |
---|---|
JP (1) | JPS5452003A (en) |
AU (1) | AU522378B2 (en) |
CA (1) | CA1102795A (en) |
DE (1) | DE2834999A1 (en) |
FI (1) | FI782477A (en) |
FR (1) | FR2400552A1 (en) |
SE (1) | SE417441B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2010104444A1 (en) | 2009-03-11 | 2010-09-16 | Swedish Oat Fiber Ab | Method for separating neutral and polar lipids and an oil rich in polar lipids |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2676936B1 (en) * | 1991-05-27 | 1993-11-05 | Inocosm Laboratoires | PROCESS FOR SEPARATING A COMPOUND RICH IN GLYCOLIPIDES LYSOPHOSPHOLIPIDES SHINGOLIPIDES AND CERAMIDES OF PLANT ORIGIN, AS WELL AS COSMETIC PRODUCTS OBTAINED BY THE IMPLEMENTATION OF THIS PROCESS. |
DE59506314D1 (en) * | 1994-08-16 | 1999-08-05 | Frische Gmbh | METHOD FOR OBTAINING NON-WATER-SOLUBLE, NATURAL PRODUCTS FROM NATURAL MIXTURES WITH THE AID OF THE CENTRIFUGAL FORCE |
AU6987996A (en) * | 1995-09-14 | 1997-04-01 | Unilever N.V. | Surface-active composition |
FR2836335B1 (en) * | 2002-02-27 | 2004-12-03 | Intersnack Knabber Geback Gmbh | STARCH-BASED DEHYDRATED FLAKES COMPRISING 0.05% GLYCOLIPIDE (S) |
CA2481411C (en) | 2002-04-19 | 2016-06-14 | Diversa Corporation | Phospholipases, nucleic acids encoding them and methods for making and using them |
US7226771B2 (en) | 2002-04-19 | 2007-06-05 | Diversa Corporation | Phospholipases, nucleic acids encoding them and methods for making and using them |
DK2853593T3 (en) | 2003-03-07 | 2018-01-08 | Dsm Ip Assets Bv | Hydrolases, nucleic acids encoding them, and processes for their preparation and use |
CN103173282A (en) | 2004-06-16 | 2013-06-26 | 帝斯曼知识产权资产管理有限公司 | Compositions and methods for enzymatic decolorization of chlorophyll |
US20080070291A1 (en) | 2004-06-16 | 2008-03-20 | David Lam | Compositions and Methods for Enzymatic Decolorization of Chlorophyll |
WO2007092314A2 (en) | 2006-02-02 | 2007-08-16 | Verenium Corporation | Esterases and related nucleic acids and methods |
MX2009003034A (en) | 2006-09-21 | 2009-11-18 | Verenium Corp | Phospholipases, nucleic acids encoding them and methods for making and using them. |
UA109884C2 (en) | 2009-10-16 | 2015-10-26 | A POLYPEPTIDE THAT HAS THE ACTIVITY OF THE PHOSPHATIDYLINOSYTOL-SPECIFIC PHOSPHOLIPASE C, NUCLEIC ACID, AND METHOD OF METHOD | |
UA111708C2 (en) | 2009-10-16 | 2016-06-10 | Бандж Ойлз, Інк. | METHOD OF OIL REFINING |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR1469392A (en) * | 1965-02-20 | 1967-02-10 | Inst Przemyslu Tluszczowego | Continuous process for the degumming of vegetable oils and for the production of lecithin from the phosphatide sludge obtained, and device for implementing this process |
DE1923971B1 (en) * | 1969-05-10 | 1970-11-26 | Heinz Schumacher | Method and device for degumming vegetable oils |
-
1977
- 1977-08-19 SE SE7709374A patent/SE417441B/en not_active IP Right Cessation
-
1978
- 1978-08-04 AU AU38631/78A patent/AU522378B2/en not_active Expired
- 1978-08-10 DE DE19782834999 patent/DE2834999A1/en active Granted
- 1978-08-14 FI FI782477A patent/FI782477A/en unknown
- 1978-08-14 CA CA309,300A patent/CA1102795A/en not_active Expired
- 1978-08-17 FR FR7824047A patent/FR2400552A1/en active Granted
- 1978-08-18 JP JP10136578A patent/JPS5452003A/en active Granted
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2010104444A1 (en) | 2009-03-11 | 2010-09-16 | Swedish Oat Fiber Ab | Method for separating neutral and polar lipids and an oil rich in polar lipids |
EP3816265A1 (en) | 2009-03-11 | 2021-05-05 | Swedish Oat Fiber AB | Method for separating neutral and polar lipids and an oil rich in polar lipids |
Also Published As
Publication number | Publication date |
---|---|
AU3863178A (en) | 1980-02-07 |
SE7709374L (en) | 1979-02-20 |
JPS626558B2 (en) | 1987-02-12 |
JPS5452003A (en) | 1979-04-24 |
CA1102795A (en) | 1981-06-09 |
FR2400552A1 (en) | 1979-03-16 |
FI782477A (en) | 1979-02-20 |
DE2834999C2 (en) | 1989-04-20 |
AU522378B2 (en) | 1982-06-03 |
FR2400552B1 (en) | 1983-08-05 |
DE2834999A1 (en) | 1979-03-01 |
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