CN101033243A - Method of coproducting phytosterol, biological diesel oil and vitamin E - Google Patents
Method of coproducting phytosterol, biological diesel oil and vitamin E Download PDFInfo
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- CN101033243A CN101033243A CNA200710014171XA CN200710014171A CN101033243A CN 101033243 A CN101033243 A CN 101033243A CN A200710014171X A CNA200710014171X A CN A200710014171XA CN 200710014171 A CN200710014171 A CN 200710014171A CN 101033243 A CN101033243 A CN 101033243A
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- plant sterol
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E50/00—Technologies for the production of fuel of non-fossil origin
- Y02E50/10—Biofuels, e.g. bio-diesel
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/54—Improvements relating to the production of bulk chemicals using solvents, e.g. supercritical solvents or ionic liquids
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P30/00—Technologies relating to oil refining and petrochemical industry
- Y02P30/20—Technologies relating to oil refining and petrochemical industry using bio-feedstock
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- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
This invention provides a method to produce phytosterols, biodiesel and vitamin E together, and its characters: (1) conducting esterification on plants oil by-products and low carbon alcohol, washing the products and removing water on layer, recovering the lower carbon alcohol under 40 ~ 60deg.C and 0.6~0.8 ATM, the remained liquid is stored at 3~5deg.C for 8~24 hours for sucking filtration to get phytosterols, (2) locating the filtrate in the extraction reactor with supercritical carbon dioxide to extract biodiesel at 30~80deg.C, 9~15MPa, (3) increasing the pressure of reactor to 20~35MPa, to extract vitamin E at 30~80deg.C.
Description
Affiliated technical field
The invention provides a plant sterols, biofuel and vitamin-E co-production, belong to agricultural and sideline resources processing technical field.
Background technology
At present, in food service industry, protective foods industry particularly, supply falls short of demand for vitamin-E and plant sterol.The preparation method of vitamin-E generally adopts supercritical extraction method at present, but its facility investment is higher, causes the vitamin-E product price also higher, and the condition pressure of overcritical preparation vitamin-E is higher, and the time is long partially.Plant sterol preparation method complexity, technology is loaded down with trivial details.Simultaneously, fatty acid methyl ester is main biofuel, then is to alleviate one of effective means of domestic and international petrifaction diesel crisis.At present, the main bottleneck of using as the biofuel of pointing out in beautiful " the application present situation and the development prospect of the biofuel " literary composition delivered on " world agriculture " of Lee's generation is that its cost is higher, how head it off is related to the popularization and the development of biofuel.The method that reduces the production of biodiesel cost now mainly contains state subsidies, adopt food and beverage waste oil and grease to do raw material etc., yet these measures all can not fundamentally solve the higher problem of biofuel cost, because waste cooking oil has increased production process, and then have increased production cost; And state subsidies are not long-term solution after all.Simultaneously, esterification temperature is higher among the preparation method of biofuel at present, has increased facility investment expense and production run expense.
Summary of the invention
The purpose of this invention is to provide and a kind ofly can overcome plant sterol, biofuel and the vitamin-E co-production that above-mentioned defective, production cost are low, technology is simplified.Its technical scheme is:
One plant sterols, biofuel and vitamin-E co-production, it is characterized in that adopting following steps: (1) carries out esterification with Vegetable oil lipoprotein by product and low-carbon alcohol, the esterification products of gained is through washing and after layering dewaters, reclaim methyl alcohol down in 40～60 ℃, 0.6～0.8 normal atmosphere, surplus liquid is suction filtration behind-3 ℃～5 ℃ storage 8～24h, gets plant sterol; (2) suction filtration gained filtrate is placed the supercritical carbon dioxide extraction still, in 30～80 ℃ of temperature, 9～15MPa extract biofuel; (3) again extraction kettle is boosted to 20～35MPa, obtain vitamin-E in 30～80 ℃ of extractions.
Described plant sterol, biofuel and vitamin-E co-production, the Vegetable oil lipoprotein by product is pressed the two-step approach esterification in the step 1, the first step esterification free fatty acids, the second step esterification glyceryl ester.Wherein esterification free fatty acids technology be with Vegetable oil lipoprotein by product and low-carbon alcohol with 1: 2.5～4 mixed in molar ratio after, add strong acid catalyst, strong acid catalyst is a kind of of sulfuric acid, hydrochloric acid, its consumption is 2～4% of a Vegetable oil lipoprotein by product quality, in temperature is 45～70 ℃ of esterification 2～4h, 50～80 ℃ are washed to neutrality then, after layering removes and anhydrates again, reclaim low-carbon alcohol down in 50～60 ℃, 0.1～0.4 normal atmosphere; Esterification glyceryl ester technology is: with remaining Vegetable oil lipoprotein by product and low-carbon alcohol after the first step esterification free-fat acid recovery low-carbon alcohol with 1: 3～5 mixed in molar ratio after, add alkali catalyst, alkali catalyst is a kind of of potassium hydroxide, sodium methylate, its consumption is 1～2.5% of a Vegetable oil lipoprotein by product quality, in temperature is 45～85 ℃ of esterification 0.5～4h, 50～80 ℃ are washed to neutrality then, after layering removes and anhydrates again, reclaim low-carbon alcohol down in 50～60 ℃, 0.1～0.4 normal atmosphere.
Described plant sterol, biofuel and vitamin-E co-production, the supercritical extraction temperature is 50～80 ℃ in the step 2, extraction pressure 9～15MPa, 30～50 ℃ of separation temperatures are separated pressure 7～8MPa, and the extraction time is not for being extracted out to there being extract.
Described plant sterol, biofuel and vitamin-E co-production, in the step 3, supercritical extraction pressure 25～35MPa, 60～80 ℃ of extraction temperature, 30～50 ℃ of separation temperatures, separate pressure 7～8MPa, carrying agent is ethanol, its consumption be in the step 2 the filtrate quality 3～5%, carry after agent squeezes into extraction kettle, after leaving standstill extraction 0.5h, cycling extraction is not extracted out to there being extract.
Described plant sterol, biofuel and vitamin-E co-production, in the step 1, mixing speed is for being 30～90 commentaries on classics/min during esterification, and the Vegetable oil lipoprotein by product is one or more a mixture of soyabean deodorization distillate, vegetable seed deodorization distillate, cottonseed deodorization distillate, peanut deodorization distillate.
The present invention compared with prior art has following advantage:
1, obtain vitamin-E, plant sterol and biofuel by coproduction, technology is simple, and cost is low;
2, esterification is complete, plant sterol purity height;
3, owing to adopt supercritical carbon dioxide extraction method, the vitamin-E hazardous solvent of acquisition is residual few.
Preferred forms
Embodiment 1:
Step 1: getting 200g soyabean deodorization distillate and methyl alcohol, to place temperature with 1: 3 mixed in molar ratio be 65 ℃ esterification device, add the 4g vitriol oil again, esterification 3h under the stirring velocity of 80 commentaries on classics/min, 78 ℃ are washed to neutrality then, treat layering remove anhydrate after, reclaim down methyl alcohol in 60 ℃, 0.3 normal atmosphere; The esterification glyceryl ester stage, it is 46 ℃ esterification device that remaining soyabean deodorization distillate and methyl alcohol behind the first step esterification free-fat acid recovery methyl alcohol are placed temperature with 1: 4 mixed in molar ratio, add 5g potassium hydroxide again, esterification time 2h, 80 ℃ are washed to neutrality then, treat layering remove anhydrate after, reclaim down methyl alcohol in 50 ℃, 0.4 normal atmosphere, surplus liquid is stored suction filtration behind the 14h in 0 ℃ of refrigerator, the plant sterol 33g of content 93%.
Step 2: the separating still that suction filtration gained filtrate is placed 65 ℃ of supercritical temperatures, pressure 10MPa, 45 ℃ of separation temperatures, separation pressure 8MPa, 1.25h altogether till being extracted to no extract and being extracted out, in the separating still fatty acid methyl ester is 85% biofuel 154g.
Step 3: break the 8mL dehydrated alcohol to extraction kettle with auxiliary pump, overcritical device extraction kettle boosts to 28MPa, is warmed up to 75 ℃, 30 ℃ of separating still temperature, pressure 8MPa, the extraction time is 1.75h altogether till do not have extract and be extracted out, in the separating still mass content is 47% vitamin e1 4g.
Embodiment 2:
Step 1: getting 200g vegetable seed deodorization distillate and ethanol, to place temperature with 1: 4 mixed in molar ratio be 45 ℃ esterification device, add the 10g vitriol oil again, esterification 4h under the stirring velocity of 40 commentaries on classics/min, 50 ℃ are washed to neutrality then, treat layering remove anhydrate after, reclaim down ethanol in 65 ℃, 0.3 normal atmosphere; The esterification glyceryl ester stage, with remaining vegetable seed deodorization distillate behind the first step esterification free-fat acid recovery ethanol, placing temperature by vegetable seed deodorization distillate and ethanol with 1: 5 mixed in molar ratio is 75 ℃ esterification device, add vegetable seed deodorization distillate quality 1% sodium methylate again, esterification time 4h, 60 ℃ are washed to neutrality then, treat layering remove anhydrate after, reclaim down ethanol in 60 ℃, 0.1 normal atmosphere, suction filtration behind 5 ℃ of storages of surplus liquid 14h, the plant sterol 35g of content 90%.
Step 2: the separating still that the filtrate of suction filtration gained is placed 75 ℃ of supercritical temperatures, pressure 13MPa, 30 ℃ of separation temperatures, separation pressure 7MPa, 1h altogether till being extracted to no extract and being extracted out, in the separating still fatty-acid ethyl ester content is 85% biofuel 158g.
Step 3: break the 10mL dehydrated alcohol to extraction kettle with auxiliary pump, overcritical device extraction kettle boosts to 32MPa, is warmed up to 75 ℃, 50 ℃ of separating still temperature, pressure 7MPa, the extraction time is 1.5h altogether till do not have extract and be extracted out, in the separating still mass content is 49% vitamin e1 1g.
Claims (10)
1, a plant sterols, biofuel and vitamin-E co-production, it is characterized in that adopting following steps: (1) carries out esterification with Vegetable oil lipoprotein by product and low-carbon alcohol, the esterification products of gained is through washing and after layering dewaters, reclaim low-carbon alcohol down in 40～60 ℃, 0.6～0.8 normal atmosphere, surplus liquid is suction filtration behind-3 ℃～5 ℃ storage 8～24h, gets plant sterol; (2) suction filtration gained filtrate is placed the supercritical carbon dioxide extraction still, in 30～80 ℃ of temperature, 9～15MPa extract biofuel; (3) again extraction kettle is boosted to 20～35MPa, obtain vitamin-E in 30～80 ℃ of extractions.
2, vitamin-E according to claim 1, plant sterol and biofuel co-production is characterized in that: in the step 1, the Vegetable oil lipoprotein by product is pressed the two-step approach esterification, the first step esterification free fatty acids, the second step esterification glyceryl ester.
3, plant sterol according to claim 2, biofuel and vitamin-E co-production, it is characterized in that esterification free fatty acids technology is in the step 1: with Vegetable oil lipoprotein by product and low-carbon alcohol with 1: 2.5～4 mixed in molar ratio after, add strong acid catalyst, the strong acid catalyst consumption is 2～4% of a Vegetable oil lipoprotein by product quality, in temperature is 45～70 ℃ of esterification 2～4h, 50～80 ℃ are washed to neutrality then, after layering removes and anhydrates again, reclaim low-carbon alcohol down in 50～60 ℃, 0.1～0.4 normal atmosphere.
4, plant sterol according to claim 3, biofuel and vitamin-E co-production is characterized in that: strong acid catalyst is a kind of of sulfuric acid, hydrochloric acid.
5, plant sterol according to claim 2, biofuel and vitamin-E co-production, it is characterized in that esterification glyceryl ester technology is in the step 1: with remaining Vegetable oil lipoprotein by product and low-carbon alcohol after the first step esterification free-fat acid recovery low-carbon alcohol with 1: 3～5 mixed in molar ratio after, add alkali catalyst, the alkali catalyst consumption is 1～2.5% of a Vegetable oil lipoprotein by product quality, in temperature is 45～85 ℃ of esterification 0.5～4h, 50～80 ℃ are washed to neutrality then, after layering removes and anhydrates again, in 50～60 ℃, 0.1～0.4 normal atmosphere reclaims low-carbon alcohol down.
6, plant sterol according to claim 5, biofuel and vitamin-E co-production is characterized in that: alkali catalyst is a kind of of potassium hydroxide, sodium methylate.
7, plant sterol according to claim 1, biofuel and vitamin-E co-production, it is characterized in that: the supercritical extraction temperature is 50～80 ℃ in the step 2, extraction pressure 9～15MPa, 30～50 ℃ of separation temperatures, separate pressure 7～8MPa, the extraction time is not for being extracted out to there being extract.
8, plant sterol according to claim 1, biofuel and vitamin-E co-production, it is characterized in that: in the step 3, supercritical extraction pressure 25～35MPa, 60～80 ℃ of extraction temperature, 30～50 ℃ of separation temperatures, separate pressure 7～8MPa, carrying agent is ethanol, its consumption be in the step 2 the filtrate quality 3～5%, carry after agent squeezes into extraction kettle, after leaving standstill extraction 0.5h, cycling extraction is not extracted out to there being extract.
9, plant sterol according to claim 1, biofuel and vitamin-E co-production is characterized in that: in the step 1, mixing speed is 30～90 commentaries on classics/min during esterification.
10, plant sterol according to claim 1, biofuel and vitamin-E co-production is characterized in that: the Vegetable oil lipoprotein by product is one or more a mixture of soyabean deodorization distillate, vegetable seed deodorization distillate, cottonseed deodorization distillate, peanut deodorization distillate in the step 1.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB200710014171XA CN100537592C (en) | 2007-04-10 | 2007-04-10 | Method of coproducting phytosterol, biological diesel oil and vitamin E |
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| Application Number | Priority Date | Filing Date | Title |
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| CNB200710014171XA CN100537592C (en) | 2007-04-10 | 2007-04-10 | Method of coproducting phytosterol, biological diesel oil and vitamin E |
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| CN101033243A true CN101033243A (en) | 2007-09-12 |
| CN100537592C CN100537592C (en) | 2009-09-09 |
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Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103045664A (en) * | 2012-12-15 | 2013-04-17 | 华中科技大学 | Method for producing biodiesel, sterol and vitamin E from deodorized distillate |
| CN105418713A (en) * | 2015-12-20 | 2016-03-23 | 高大元 | Preparation method of water-soluble amino acid modified soyasterol of caviar |
| CN109456382A (en) * | 2018-12-18 | 2019-03-12 | 湖南科瑞生物制药股份有限公司 | A method of preparing delmadinone acetate |
| CN109535214A (en) * | 2018-12-18 | 2019-03-29 | 湖南科瑞生物制药股份有限公司 | A method of preparing the bis- dehydrogenation -17a- hydroxyl progesterones of 1,6- |
| CN109627275A (en) * | 2018-12-18 | 2019-04-16 | 湖南科瑞生物制药股份有限公司 | A kind of bis- dehydrogenation -17a- hydroxyl progesterone product preparation methods of 1,6- |
| CN109627276A (en) * | 2018-12-18 | 2019-04-16 | 湖南科瑞生物制药股份有限公司 | It is a kind of to prepare the bis- dehydrogenation -17a- hydroxyl progesterone method for product of 1,6- |
| CN109651473A (en) * | 2019-02-18 | 2019-04-19 | 湖南科瑞生物制药股份有限公司 | A kind of preparation method of androstane -2- alkene -17- ketone |
| CN111875657A (en) * | 2020-07-31 | 2020-11-03 | 福建省格兰尼生物工程股份有限公司 | Deodorized distillate suitable for biological enzyme esterification reaction and preparation method thereof |
| CN114409719A (en) * | 2022-01-24 | 2022-04-29 | 浙江工业大学 | Method for extracting phytosterol from rice bran oil deodorizer distillate |
| CN114921283A (en) * | 2015-09-30 | 2022-08-19 | 公立大学法人大阪 | Method and apparatus for producing vegetable oil |
-
2007
- 2007-04-10 CN CNB200710014171XA patent/CN100537592C/en not_active Expired - Fee Related
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103045664A (en) * | 2012-12-15 | 2013-04-17 | 华中科技大学 | Method for producing biodiesel, sterol and vitamin E from deodorized distillate |
| CN114921283A (en) * | 2015-09-30 | 2022-08-19 | 公立大学法人大阪 | Method and apparatus for producing vegetable oil |
| CN105418713A (en) * | 2015-12-20 | 2016-03-23 | 高大元 | Preparation method of water-soluble amino acid modified soyasterol of caviar |
| CN109456382A (en) * | 2018-12-18 | 2019-03-12 | 湖南科瑞生物制药股份有限公司 | A method of preparing delmadinone acetate |
| CN109535214A (en) * | 2018-12-18 | 2019-03-29 | 湖南科瑞生物制药股份有限公司 | A method of preparing the bis- dehydrogenation -17a- hydroxyl progesterones of 1,6- |
| CN109627275A (en) * | 2018-12-18 | 2019-04-16 | 湖南科瑞生物制药股份有限公司 | A kind of bis- dehydrogenation -17a- hydroxyl progesterone product preparation methods of 1,6- |
| CN109627276A (en) * | 2018-12-18 | 2019-04-16 | 湖南科瑞生物制药股份有限公司 | It is a kind of to prepare the bis- dehydrogenation -17a- hydroxyl progesterone method for product of 1,6- |
| CN109651473A (en) * | 2019-02-18 | 2019-04-19 | 湖南科瑞生物制药股份有限公司 | A kind of preparation method of androstane -2- alkene -17- ketone |
| CN111875657A (en) * | 2020-07-31 | 2020-11-03 | 福建省格兰尼生物工程股份有限公司 | Deodorized distillate suitable for biological enzyme esterification reaction and preparation method thereof |
| CN114409719A (en) * | 2022-01-24 | 2022-04-29 | 浙江工业大学 | Method for extracting phytosterol from rice bran oil deodorizer distillate |
| CN114409719B (en) * | 2022-01-24 | 2023-12-12 | 浙江工业大学 | Method for extracting phytosterol from rice bran oil deodorized distillate |
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| CN100537592C (en) | 2009-09-09 |
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