CN1309727C - Method for preparing powdery phosphatide by alkali emulsion phosphatide - Google Patents
Method for preparing powdery phosphatide by alkali emulsion phosphatide Download PDFInfo
- Publication number
- CN1309727C CN1309727C CNB2004100242238A CN200410024223A CN1309727C CN 1309727 C CN1309727 C CN 1309727C CN B2004100242238 A CNB2004100242238 A CN B2004100242238A CN 200410024223 A CN200410024223 A CN 200410024223A CN 1309727 C CN1309727 C CN 1309727C
- Authority
- CN
- China
- Prior art keywords
- phosphatide
- acetone
- phospholipid
- alkalization
- emulsus
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
Landscapes
- Fats And Perfumes (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
Abstract
The present invention provides a method for preparing powdery phospholipid by alkalized milky phospholipid as raw materials, and the alkalized milky phospholipid is prepared from alkalized oil sediments of different plants of peanuts, soybeans, vegetable seeds, etc. Acetone is added into an extracting container according to a proportion of the alkalized milky phospholipid and the acetone; under the condition of stir, the alkalized milky phospholipid is added; the alkalized milky phospholipid and the acetone are stirred, extracted and settled; under the condition of continuous stir, precipitates are extracted by the acetone until supernatant liquid is almost colorless and transparent, different processing agents which are favorable to producing the powdery phospholipid are added, and the method for preparing powdery phospholipid by the alkalized milky phospholipid raw materials has the advantages of easy production, high efficiency and low cost.
Description
Technical field
The present invention relates to produce the method for powder lecithin, the alkalization emulsus phosphatide that especially a kind of alkalization oil foot that utilizes different plants such as peanut, soybean, vegetable seed is made is the method for the Powdered phosphatide of raw material production.
Background technology
Extract preparation powder soybean phospholipid solvent for use and be the existing many reports of acetone (Zhao Yingju etc. medicinal soybean lecithin refining. animal doctor's college journal .13 (4) 372-375.1993).Tong Qigen (production method of novel high quality soy phosphatide, foodstuffs industry science and technology (7) .18-23.1990) proposes with ether-when the acetone-water method prepares the powder soybean phospholipid except that deoiling, and the fractionation relative complex of ether-acetone.Ni Hongzhi (solvent method of phosphatide is refining and separates. Chinese oil 10 (3) .50-52.1991) propose with the yield that can increase substantially phosphatide after the acetone oil removing once again with water treatment, but more than having dewatered then during again with acetone extract a dewatering process.The phosphatide color and luster is dark when using acetone deoiling once more, and the acetone consumption does not reduce.Wang Jingshi (preparation of soybean phospholipid and application. chemical and bonding. (1) .1991.36-40) with 5 ℃ of acetone extraction powdered soybean phospholipids,, but must have freezer in process of production because this moment, solubleness was 0.003%.Temperature light source etc. (the reparation technology experiment of powder soybean phospholipid. Chinese oil 1985 (5) .40-47), Zhang Genwang etc. (development of human consumption soybean phosphatide. Zhengzhou Grain College journal 1991 (2) .1-8) carry out powder soybean phospholipid pilot experiment with acetone as solvent, spray strip device and the circulation device except that the latter increases a material separating disc at stirring feed solution mouth, other parts of technology do not have big-difference.But the two all makes raw material with soybean aquation concentrated phosphatide.Up till now, making raw material in China with soybean aquation concentrated phosphatide adopts acetone extract explained hereafter powder lecithin to be accepted by producer.But now the above grease of China 90% factory takes alkali addition process.Alkalization oil foot or by its alkalization emulsus phosphatide that is processed into, perhaps the emulsus phosphatide producer of hydrated oil foot preparation has added alkali therein for reducing acid number.It is then very difficult to adopt above production technique to make powder soybean phosphine fat.Saponified and the normal phosphatide of glyceride can not form powder when mixing oven dry.Utilizing the alkalization oil foot to prepare the powder soybean phospholipid is to require study and the wide new technology of market outlook.Liu the present inventor obviously improves with alkalization emulsus phosphatide production powder lecithin effect for the powder lecithin working system that becomes once to have invented a kind of suitable different plant emulsification phosphatide raw materials (Chinese patent application number be 200310105345.5).About 1 ton 500 yuan of alkalization oil foot prices, the about 1 ton of 2000-2500 unit of the alkalization emulsus phosphatide that is processed into thus, and 1 ton/3000-4000 of aquation emulsus phosphatide price unit.
Summary of the invention:
The purpose of this invention is to provide and a kind ofly just utilizing the solvent acetone emulsus phosphatide that will alkalize to be extracted to the roughly water white front and back of supernatant liquor and to add the processing aid that is beneficial to powdered phospholipid production, make alkalization emulsus phosphatide raw material production powder lecithin easier, the more effective technology that becomes simple, the method for easy handling.
Purpose of the present invention can realize by following technical measures
Earlier with the proportioning adding extraction container of acetone according to alkalization emulsus phosphatide and acetone, add alkalization emulsus phosphatide down in stirring again, stir extraction, leave standstill, when again throw out being extracted to the supernatant liquor water white transparency continuously with acetone under stirring, getting the precipitated liquid that contains powdered phospholipid and be sent from scheming, the phosphatide after centrifugal is joined to be dissolved with according to dry powder phosphatide amount be in the mellisic acetone solution of 100 0.01~0.1 weight part, under agitation be cooled to normal temperature, centrifugal drying gets powder lecithin.
The described temperature that is dissolved with the mellisic acetone solution is 50-55 ℃.
The alkalization emulsus phosphatide that the present invention adopts the alkalization oil foot to make is that the raw material production powder lecithin not only greatly reduces production cost, and the separation of solvent in convenient the production, do not need other auxiliary processes and equipment, just utilizing the solvent acetone emulsus phosphatide that will alkalize to be extracted to the roughly water white front and back of supernatant liquor and to add the processing aid that is beneficial to powdered phospholipid production, make alkalization emulsus phosphatide raw material production powder lecithin become easier, more effective, cost is lower.
Embodiment:
Embodiment 1
It is the emulsus phosphatide (moisture do not surpass 2%) of alkalization soybean oil residue preparation that the present invention adopts raw material, the extraction solvent is an acetone, earlier by alkalization emulsus phosphatide: the weight part proportioning of acetone=1: 10, acetone is pumped into the stirring extractor, begin to stir, stirring velocity 80r/min pumps into alkalization emulsus phosphatide (pressing 10Kg/min speed) while stirring.Stir extraction 0.5 hour behind the intact alkalization of the pump emulsus phosphatide, stop to stir, static avaling 15 minutes emitted supernatant liquid.Second and third, extract used amounts of acetone for four, five times and be respectively 5,5,5,2 times of alkalization emulsus phosphatide parts by weight of raw materials, stir the extraction time and static, sinking time is same as described above.During the supernatant liquor water white transparency, the precipitated liquid that contains powdered phospholipid under agitation can be emitted and adds whizzer, centrifugal (1400r/min) 5 minutes by extractor to the end.Phosphatide is the powder agglomates shape, then it being joined 50 ℃ is dissolved with the mellisic acetone soln (the beeswax amount is a dry powder phosphatide: beeswax=100: 0.01 weight parts), stirred 10 minutes, evenly, be cooled to normal temperature while stirring, static, avale, emit the supernatant acetone solution after, stir and to emit the precipitated liquid that lower floor contains powdered phospholipid, centrifugal (1400r/min) 5 minutes down, be paved into 1cm thickness, dried 15 minutes for 55 ℃, or adopt the dry 30 ℃ of dry powdereds of vacuum of bipyramid, packing then.The content of soybean composite phospholipid in powder lecithin is generally about 95%.
As being raw material with the soybean oil residue, oil foot can be poured into 45 ℃ of insulations of jacketed kettle 24 hours, inclining upper strata fluid, then lower floor is contained phosphatide liquid and steams moisture one-tenth alkalization emulsus phosphatide through horizontal wiped film vaporization equipment.Also can directly use alkalization oil foot direct production, but the acetone consumption is excessive, the powdered phospholipid productive rate is low, and cost is too high.
Vegetable seed and arachine carburetion pin and alkalization emulsus phosphatide are handled with soybean alkalization emulsus phosphatide, and the phospholipids content of the peanut powdered phospholipid of production is about 90%, and the phospholipids content of the vegetable seed powdered phospholipid of production is about 93%.
Embodiment 2
Raw materials used and extraction process is all with embodiment 1, being the blocky phosphatide of powder after just will extracting joins 52 ℃ and is dissolved with the mellisic acetone soln (the beeswax amount is a dry powder phosphatide: beeswax=100: 0.05 weight parts), stirred 20 minutes, evenly, be cooled to normal temperature while stirring, static, avale, emit the supernatant acetone solution after, stir and emit the precipitated liquid that lower floor contains powdered phospholipid down, centrifugal (1400r/min) 8 minutes, after be paved into 60 ℃ of 1.5cm thickness oven dry 15 minutes, or adopt the dry 45 ℃ of dry powdereds of vacuum of bipyramid, pack then.The content of soybean composite phospholipid in powder lecithin is generally about 95%.
Embodiment 3
Raw materials used and extraction process is all with embodiment 1, being the blocky phosphatide of powder after just will extracting joins 55 ℃ and is dissolved with the mellisic acetone soln (the beeswax amount is a dry powder phosphatide: beeswax=100: 0.1 weight parts), stirred 30 minutes, evenly, be cooled to normal temperature while stirring, static, avale, emit the supernatant acetone solution after, stir and emit the precipitated liquid that lower floor contains powdered phospholipid down, centrifugal (1400r/min) 10 minutes, after be paved into 65 ℃ of 2cm thickness oven dry 15 minutes, or adopt the dry 60 ℃ of dry powdereds of vacuum of bipyramid, pack then.The content of soybean composite phospholipid in powder lecithin is generally about 95%.
As being raw material with the soybean oil residue, oil foot can be poured into 70 ℃ of insulations of jacketed kettle 48 hours, inclining upper strata fluid, then lower floor is contained phosphatide liquid and steams moisture one-tenth alkalization emulsus phosphatide through horizontal wiped film vaporization equipment.
Claims (2)
1, the method for utilizing alkalization emulsus phosphatide to produce powder lecithin, earlier with the proportioning adding extraction container of acetone according to alkalization emulsus phosphatide and acetone, add alkalization emulsus phosphatide down in stirring again, stir extraction, leave standstill, when again throw out being extracted to the supernatant liquor water white transparency continuously with acetone under stirring, get the precipitated liquid that contains powdered phospholipid and be sent from scheming, phosphatide after centrifugal joined to be dissolved with according to dry powder phosphatide amount be in the mellisic acetone solution of 100 0.01~0.1 weight part, under agitation be cooled to normal temperature, centrifugal drying gets powder lecithin.
2, the method for utilization alkalization emulsus phosphatide production powder lecithin according to claim 1 is characterized in that the described temperature that is dissolved with the mellisic acetone solution is 50-55 ℃.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB2004100242238A CN1309727C (en) | 2004-06-01 | 2004-06-01 | Method for preparing powdery phosphatide by alkali emulsion phosphatide |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB2004100242238A CN1309727C (en) | 2004-06-01 | 2004-06-01 | Method for preparing powdery phosphatide by alkali emulsion phosphatide |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1583765A CN1583765A (en) | 2005-02-23 |
CN1309727C true CN1309727C (en) | 2007-04-11 |
Family
ID=34600835
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB2004100242238A Expired - Fee Related CN1309727C (en) | 2004-06-01 | 2004-06-01 | Method for preparing powdery phosphatide by alkali emulsion phosphatide |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN1309727C (en) |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1270030A (en) * | 2000-03-23 | 2000-10-18 | 张文芳 | Process for preparing high-purity phosphatide particles directly from concentrated phosphatide |
CN1408716A (en) * | 2001-09-25 | 2003-04-09 | 上海金伴药业有限公司 | Process for preparing powdered soy bean phosphatide |
-
2004
- 2004-06-01 CN CNB2004100242238A patent/CN1309727C/en not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1270030A (en) * | 2000-03-23 | 2000-10-18 | 张文芳 | Process for preparing high-purity phosphatide particles directly from concentrated phosphatide |
CN1408716A (en) * | 2001-09-25 | 2003-04-09 | 上海金伴药业有限公司 | Process for preparing powdered soy bean phosphatide |
Also Published As
Publication number | Publication date |
---|---|
CN1583765A (en) | 2005-02-23 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN103859067B (en) | A kind of nutrition Rice oil and production method thereof | |
CN102191128B (en) | Method for preparing edible idesia oil | |
CN102676291A (en) | Method for extracting antarctic krill grease and separating biological active substance | |
CN101401658A (en) | Medium test method for extracting oil and protolysate from peanut with water-enzyme method | |
CN101343309B (en) | Method for simultaneously separating soy protein and oil fat with inverse micelle abstraction technique | |
CN102550708A (en) | Method for preparing Cyperus esculentus edible oil | |
CN108753453A (en) | Shinyleaf yellowhorn oil refinery practice | |
CN102311867A (en) | Method for extracting Cyperus esculentus oil by aqueous enzymatic extraction-freeze-thaw coupling technology | |
CN104711124A (en) | Soybean lecithin processing technology | |
CN108902441A (en) | A kind of flaxseed meal deep working method | |
CN104651040A (en) | Method for degumming fragrant rap oil through enzymic process | |
CN108276438A (en) | A kind of preparation method and applications of EPA plasmalogens | |
Wu et al. | Fractionation of crude soybean lecithin with aqueous ethanol | |
CN103361171B (en) | Method for preparing rice bran oil, rice bran protein and phytin from rice bran | |
CN1309727C (en) | Method for preparing powdery phosphatide by alkali emulsion phosphatide | |
CN104041655B (en) | A kind of production method of soybean protein isolate | |
CN101016228A (en) | Policosanol prepared from sugarcane epidermis and preparing method thereof | |
CN104711112A (en) | Method for realization of combined production of high quality rice bran oil and ferulic acid from rice bran | |
CN1272335C (en) | Method of producing powder phosphatide using of peanut, soyabeun, repeseed phosphatide from milky | |
CN110862862A (en) | Method for simultaneously preparing xanthoceras sorbifolia Bunge oil and xanthoceras sorbifolia Bunge protein by aqueous enzymatic method | |
CN1285277C (en) | Production of powdery lipoid | |
CN101796983A (en) | Novel preparation technology of vegetable health care oil | |
CN103773596A (en) | Preparation method of krill oil | |
CA2948964C (en) | Method for obtaining sinapic acid from a native material mixture | |
CN1742604A (en) | Method for preparing composite vegetable-seed polypeptide through peeling vegetable-seed and cold squeezing |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
C19 | Lapse of patent right due to non-payment of the annual fee | ||
CF01 | Termination of patent right due to non-payment of annual fee |