CN101338212A - Method for preparing biodesel - Google Patents
Method for preparing biodesel Download PDFInfo
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- CN101338212A CN101338212A CNA2007101184159A CN200710118415A CN101338212A CN 101338212 A CN101338212 A CN 101338212A CN A2007101184159 A CNA2007101184159 A CN A2007101184159A CN 200710118415 A CN200710118415 A CN 200710118415A CN 101338212 A CN101338212 A CN 101338212A
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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
- 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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Abstract
The invention relates to a preparation method for biological diesel oil, which comprises that: grease and alcohol are provided to a reactor for the transesterification; the biological oil and glycerol are separated and collected. The reaction temperature is 100-260 DEG C, and the reaction pressure is 0.2-7MPa. According to the method provided by the invention, the product yield can reach to more than 80w percent. The method of the invention is especially applied to the processing of unrefined oil with high acid value. Pretreatment process with complex procedures can be avoided, and the energy consumption and the equipment investment can be lowered. Without the three wastes, the method of the invention is an environmental friendly green process.
Description
Technical field
The present invention relates to a kind of by grease and monohydroxy-alcohol prepared in reaction method of bio-diesel oil.
Background technology
Biofuel can be that triglyceride level and low-carbon alcohol are carried out transesterification reaction and made by grease, fatty acid ester and mono-glycerides, two sweet esters, glycerine, pure and mild unreacted triglyceride level are arranged in the reaction product, can obtain biofuel by separating, wherein mainly be fatty acid ester, also contain a spot of mono-glycerides and two sweet esters.
The preparation method of biofuel can be divided into acid catalyzed process, base catalysis method, enzyme catalysis method and supercritical methanol technology.
CN1412278A discloses a kind of acid catalyzed process, with the method for preparing biological diesel oil from high acid value waste animal and plant oil, it, carries out according to the operation of raw material dehydration, esterification and transesterify, phase-splitting, decolouring as catalyzer with sulfuric acid, raw material is earlier at 60-100 ℃, dewater under the vacuum, then, under 40～85 ℃, sulfuric acid add-on 2～6%, carried out esterification and transesterification reaction 6 hours, and told the fatty acid methyl ester phase, with atlapulgite 90～125 ℃ of decolourings get final product biofuel.
It is raw material that CN1473907A adopts the tankage of vegetable oil refining and the edible oil of recovery, catalyzer is inorganic and organic acid is composite forms by sulfuric acid, hydrochloric acid, tosic acid, Witco 1298 Soft Acid, naphthene sulfonic acid etc., produce through operations such as acidifying removal of impurities, continous vacuum dehydration, esterification, layering, underpressure distillation, esterif iotacation step catalyzer add-on 1～3%, 60～80 ℃ of esterification temperatures, 6 hours reaction times.Reaction product neutralization is earlier removed catalyzer, and then, layering removes and anhydrates, and the after product that anhydrates obtains biofuel through underpressure distillation.
The acid catalysis existing problems are that speed of response is slow, have a large amount of spent acid, waste water generation in addition.
The speed of response of base catalysis method is faster than acid catalyzed process, if but free fatty acid content is more in the grease, directly use alkaline catalysts can produce fatty acid soaps, alkaline catalysts must be excessive in this case, can cause the fatty acid ester layer to separate with glycerin layer like this and become difficulty.For avoiding these problems, DE3444893 discloses a kind of method, at first, oil plant is carried out pre-esterification treatment, with acid catalyst, normal pressure, 50～120 ℃, free fatty acids and alcohol are carried out esterification, add in the excessive base metal catalysts then and the pre-residual acid catalyst of esterification, carry out transesterification reaction again, the requirement of base metal catalysts has bigger increase.Adopt that the pre-esterifying process existing problems are that technical process is long, step is many, facility investment, energy consumption significantly rise, and in addition, needs remove acid, basic catalyst from reaction process and product, need produce a large amount of waste water with a large amount of washing water.
US5713965A discloses a kind of method, in the presence of lipase, makes solvent with hexane, by grease and pure prepared in reaction fatty acid methyl ester.Though adopt the enzyme catalyst reaction conditions to relax, long reaction time, efficient are lower, need solvent, and enzyme are more expensive, easy inactivation in high purity methanol.
PCT/JP99/0543 discloses the method for a kind of grease and monohydroxy-alcohol prepared in reaction fatty acid ester, at 270～280 ℃, under 11～12MPa, methyl alcohol is reacted with oil plant, and the fatty acid methyl ester yield is 55～60%.This method severe reaction conditions is to the equipment requirements height.
Summary of the invention
The invention provides a kind ofly under than the demulcent condition, need not the high yield of catalyzer and prepare method of bio-diesel oil, not only reaction conversion ratio is near 100w%, and biofuel yield height.
The preparation method of biofuel provided by the invention comprises: provide reactor with grease and alcohol, carry out transesterification reaction, separate and collection of biological diesel oil and glycerine.
Said grease is a fatty acid triglycercide, be mainly derived from animal oil or vegetables oil, also comprise in addition from the oil plant in the materials such as microorganism, algae, acid value of oil and fat can change in the larger context, 1～190mgKOH/g for example, preferred 20～160mgKOH/g, more preferably 30～130mgKOH/g.High-acid value grease in above-mentioned acid number scope can be crude oil, waste grease or rotten grease etc.Wherein crude oil is meant without the grease that does not reach product standard after refining or refining, the refining step operations such as matter, alkali refining, dephosphorization matter, decolouring, deodorization that include but not limited to come unstuck.High-acid value grease in above-mentioned acid number scope also can obtain by the extra free fatty acids that adds in grease.
Said monohydroxy-alcohol is meant that carbon number is 1～6 Fatty Alcohol(C12-C14 and C12-C18), can be single Fatty Alcohol(C12-C14 and C12-C18), also can be the mixture of one or more Fatty Alcohol(C12-C14 and C12-C18), particular methanol and ethanol.
Said reactor is fixed-bed reactor, preferred tubular reactor.Grease and alcohol can offer reactor separately, or with offering reactor after their pre-mixings, before offering reactor, available preheater also can directly enter reactor, like this with the material preheating, reactor had both played the effect of preheater, also played the effect of reactor.As adopt preheater, preheating together after can or mixing grease and alcohol difference preheating.
100～260 ℃ of temperature of reactor, preferred 140～235 ℃, more preferably 170～220 ℃; Pressure 0.2～7MPa, preferred 1～6MPa, more preferably 2～5MPa; Oil/pure mass ratio is 0.4～8: 1, is preferably 1～7: 1, more preferably 2～7: 1.Liquid hourly space velocity is 0.1～5h
-1, preferred 0.3～2h
-1
For the reacting coarse product that obtains, can be by flash distillation, steam monohydroxy-alcohol, from the mixture behind the flash distillation monohydroxy-alcohol, separate then mixed ester mutually and glycerine mutually, can separate the separation of optimum fiber bundle by settlement separate or fibrous bundle separator, separation condition is 20～150 ℃ of temperature, preferred 40～100 ℃, pressure greater than a normal atmosphere or normal pressure all can, air speed 0.1-10h
-1, preferred 1～4h
-1Then mixed methyl phase and glycerine are distilled respectively, can be by rectification under vacuum tower or thin-film evaporator distillation, pressure is less than 0.1MPa, preferably less than 0.04MPa, reflux ratio 0.1～10 in the rectifying tower: 1, preferred 1～6: 1, tower still or thin film evaporation actuator temperature are 100～300 ℃, preferably less than 280 ℃.
According to method provided by the invention, product yield can reach more than the 80w%.Technology of the present invention is particularly suitable for processing the higher non-refining oil of acid number, can save the numerous and diverse preprocessing process of operation, and energy consumption, facility investment are descended.The basic three-waste free discharge of this technology is an eco-friendly friendly process.
Embodiment
Further specify the present invention below by example, but the present invention is not limited to this.
Relevant noun is defined as follows among the embodiment:
Yield=(biofuel weight/grease weight) * 100%
The oil quantity that liquid hourly space velocity=unit volume reactor unit time handles
W% represents weight percentage.
Embodiment 1
Grease and the methyl alcohol of acid number 104.7mgKOH/g are provided in the preheater liquid hourly space velocity 0.6h with the speed of 600 Grams Per Hours and 100 Grams Per Hours respectively
-1160 ℃ of preheater temperature, material after the preheating continuously is provided in the tubular reactor 200～205 ℃ of temperature of reaction, pressure 2.0～2.5MPa, reacting coarse product enters flashing tower, remove methyl alcohol at＜150 ℃, and methyl alcohol is reclaimed, reuses, leftover materials are entered the fibrous bundle separator, at 20 ℃ of temperature, liquid hourly space velocity 5h
-1, tell the mixed ester phase, the middle mutually content of triglyceride 2.4w% of mixed ester, mixed ester enters thin-film evaporator mutually, at pressure 6mmHg, under the condition that temperature is 240 ℃, steams biofuel, yield 85.2w%.
Embodiment 2
Grease and the methyl alcohol of acid number 58.1mgKOH/g are provided in the preheater liquid hourly space velocity 0.7h with the speed of 600 Grams Per Hours and 100 Grams Per Hours respectively
-1, 160 ℃ of preheater temperature continuously are provided to the material after the preheating in the tubular reactor, 220 ℃ of temperature of reaction, pressure 5.5～6.0MPa, the crude product of outflow reactor enters flashing tower, removes methyl alcohol and methyl alcohol is reclaimed, reuses at＜150 ℃.Leftover materials are entered the fibrous bundle separator, at 30 ℃ of temperature, liquid hourly space velocity 10h
-1Under the condition, tell continuously mixed ester mutually and glycerine mutually, the middle mutually content of triglyceride 0 of ester, mixed ester enters the rectification under vacuum tower mutually, at pressure 11mmHg, 267 ℃ of tower stills under 3: 1 the condition of reflux ratio, steam biofuel, yield 93w%.
Embodiment 3
Grease and the methyl alcohol of acid number 49.3mgKOH/g are provided in the preheater liquid hourly space velocity 0.6h with the speed of 600 Grams Per Hours and 110 Grams Per Hours respectively
-1140 ℃ of preheater temperature, continuously be provided to the material after the preheating in the tubular reactor, 200～205 ℃ of temperature of reaction, pressure 3.5～4MPa, the reacting coarse product of outflow reactor enters flashing tower, remove methyl alcohol and methyl alcohol is reclaimed, reuses at＜150 ℃, leftover materials are entered the fibrous bundle separator, at 60 ℃ of temperature, liquid hourly space velocity 5h
-1, divide the ester output phase, the middle mutually content of triglyceride 1.25w% of ester, ester enters the rectification under vacuum tower mutually, and at pressure 15mmHg, 279 ℃ of tower stills under 0.6: 1 the condition of reflux ratio, steam biofuel, and yield can reach 88.2w%.
Embodiment 4
Grease and the methyl alcohol of acid number 35.3mgKOH/g are provided in the preheater liquid hourly space velocity 0.6h with the speed of 600 Grams Per Hours and 128 Grams Per Hours respectively
-1, 140 ℃ of preheater temperature continuously are provided to the material after the preheating in the tubular reactor, temperature of reaction 225-230 ℃, pressure 0.7～0.9MPa, the crude product of outflow reactor enters flashing tower, remove methyl alcohol and methyl alcohol is reclaimed, reuses at＜150 ℃, leftover materials carry out settlement separate, divide ester output mutually with glycerine mutually, mixed ester enters thin-film evaporator mutually, at pressure 11mmHg, under the condition that temperature is 255 ℃, steam biofuel, yield 74.4w%.
Embodiment 5
Grease and the methyl alcohol of acid number 125.7mgKOH/g are provided in the preheater liquid hourly space velocity 0.6h with the speed of 600 Grams Per Hours and 100 Grams Per Hours respectively
-1, 170 ℃ of preheater temperature continuously are provided to the material after the preheating in the tubular reactor, 200～205 ℃ of temperature of reaction, pressure 3.5～4MPa, the crude product of outflow reactor separates by the method for embodiment 3, obtain biofuel, yield 71.4w%.
Embodiment 6
Grease and the methyl alcohol of acid number 81.2mgKOH/g are provided in the preheater liquid hourly space velocity 0.7h with the speed of 600 Grams Per Hours and 100 Grams Per Hours respectively
-1, 140 ℃ of preheater temperature continuously are provided to the material after the preheating in the tubular reactor, 180 ℃ of temperature of reaction, and pressure 5.8～6.0MPa, the crude product of outflow reactor separates by the method for embodiment 2, steams biofuel, yield 90.7w%.
Embodiment 7
Grease and the methyl alcohol of acid number 22.5mgKOH/g are provided in the preheater liquid hourly space velocity 0.6h with the speed of 600 Grams Per Hours and 100 Grams Per Hours respectively
-1, 170 ℃ of preheater temperature continuously are provided to the material after the preheating in the tubular reactor, 210～215 ℃ of temperature of reaction, pressure 2.0～2.5MPa, the crude product of outflow reactor separates by the method for embodiment 4, steam biofuel, yield 51.2w%.
Comparative example 1
Grease and the methyl alcohol of acid number 0.4mgKOH/g are provided in the preheater liquid hourly space velocity 0.6h with the speed of 600 Grams Per Hours and 100 Grams Per Hours respectively
-1, 170 ℃ of preheater temperature continuously are provided to the material after the preheating in the tubular reactor, 210～215 ℃ of temperature of reaction, pressure 2.0～2.5MPa, the crude product of outflow reactor separates by the method for embodiment 1, steam biofuel, yield 19.7w%.
Claims (15)
1. the preparation method of a biofuel comprises: with grease and alcohol extracting supply response device, carry out transesterification reaction, separate and collection of biological diesel oil and glycerine, said acid value of oil and fat is 1～190mgKOH/g, and temperature of reaction is 100～260 ℃, and reaction pressure is 0.2～7MPa.
2. in accordance with the method for claim 1, it is characterized in that said acid value of oil and fat is 20～160mgKOH/g.
3. in accordance with the method for claim 1, it is characterized in that said acid value of oil and fat 30～130mgKOH/g.
4. in accordance with the method for claim 1, it is characterized in that said alcohol is the Fatty Alcohol(C12-C14 and C12-C18) of carbon number 1～6.
5. in accordance with the method for claim 1, it is characterized in that said alcohol is methyl alcohol or ethanol.
6. in accordance with the method for claim 1, it is characterized in that said reactor is a tubular reactor.
7. in accordance with the method for claim 1, it is characterized in that temperature of reaction is 140～235 ℃.
8. in accordance with the method for claim 1, it is characterized in that temperature of reaction is 170～220 ℃.
9. in accordance with the method for claim 1, it is characterized in that reaction pressure is 1～6MPa.
10. in accordance with the method for claim 1, it is characterized in that reaction pressure is 2～5MPa.
11. in accordance with the method for claim 1, it is characterized in that oil/pure mass ratio is 0.4～8: 1.
12. in accordance with the method for claim 11, it is characterized in that oil/pure mass ratio is 1～7: 1.
13. in accordance with the method for claim 11, it is characterized in that oil/pure mass ratio is 2～7: 1.
14. in accordance with the method for claim 1, it is characterized in that liquid hourly space velocity is 0.1～5h
-1
15. in accordance with the method for claim 1, it is characterized in that liquid hourly space velocity is 0.3～2h
-1
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| Application Number | Priority Date | Filing Date | Title |
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| CN2007101184159A CN101338212B (en) | 2007-07-05 | 2007-07-05 | Method for preparing biodesel |
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| CN2007101184159A CN101338212B (en) | 2007-07-05 | 2007-07-05 | Method for preparing biodesel |
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| CN101338212A true CN101338212A (en) | 2009-01-07 |
| CN101338212B CN101338212B (en) | 2012-02-15 |
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Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101812375A (en) * | 2010-04-13 | 2010-08-25 | 南京工业大学 | Production method of autocatalytic esterification and ester exchange of biodiesel |
| CN101985580A (en) * | 2010-11-15 | 2011-03-16 | 江苏永林油脂化工有限公司 | Method for preparing biodiesel from low-boiling-point substance through continuous rectification of oleic acid |
| CN102649920A (en) * | 2012-05-07 | 2012-08-29 | 唐山金利海生物柴油股份有限公司 | Device and method for continuously preparing biodiesel under intermediate-temperature and medium-pressure condition |
| CN102690726A (en) * | 2012-05-29 | 2012-09-26 | 东南大学 | Method for preparing biodiesel by fixed bed catalytic membrane reactor |
| CN103756715A (en) * | 2014-01-20 | 2014-04-30 | 厦门大学 | Preparation method of high hydrocarbon |
| CN104403805A (en) * | 2014-09-29 | 2015-03-11 | 成都新柯力化工科技有限公司 | Biodiesel preparation method |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6768015B1 (en) * | 2003-05-16 | 2004-07-27 | Stepan Company | Method of making alkyl esters using pressure |
| CN100460482C (en) * | 2005-08-31 | 2009-02-11 | 中国石油化工股份有限公司 | Method of preparing organism diesel oil from mixing plant oil |
| CN1952047B (en) * | 2005-10-19 | 2010-04-21 | 中国石油化工股份有限公司 | Production process of biological diesel oil |
-
2007
- 2007-07-05 CN CN2007101184159A patent/CN101338212B/en active Active
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101812375A (en) * | 2010-04-13 | 2010-08-25 | 南京工业大学 | Production method of autocatalytic esterification and ester exchange of biodiesel |
| CN101985580A (en) * | 2010-11-15 | 2011-03-16 | 江苏永林油脂化工有限公司 | Method for preparing biodiesel from low-boiling-point substance through continuous rectification of oleic acid |
| CN102649920A (en) * | 2012-05-07 | 2012-08-29 | 唐山金利海生物柴油股份有限公司 | Device and method for continuously preparing biodiesel under intermediate-temperature and medium-pressure condition |
| CN102690726A (en) * | 2012-05-29 | 2012-09-26 | 东南大学 | Method for preparing biodiesel by fixed bed catalytic membrane reactor |
| CN103756715A (en) * | 2014-01-20 | 2014-04-30 | 厦门大学 | Preparation method of high hydrocarbon |
| CN103756715B (en) * | 2014-01-20 | 2015-11-04 | 厦门大学 | A kind of preparation method of high-carbon hydrocarbon |
| CN104403805A (en) * | 2014-09-29 | 2015-03-11 | 成都新柯力化工科技有限公司 | Biodiesel preparation method |
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| CN101338212B (en) | 2012-02-15 |
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