CN112079709A - Method for preparing 3-hydroxydecanoic acid by hydrolyzing rhamnolipid - Google Patents
Method for preparing 3-hydroxydecanoic acid by hydrolyzing rhamnolipid Download PDFInfo
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Abstract
A method of preparing 3-hydroxydecanoic acid from rhamnolipid hydrolysis, the method comprising: 1) the rhamnolipid aqueous solution is subjected to hydrolysis reaction under the catalysis of acid to obtain a water phase containing rhamnose and an oil phase containing 3-hydroxydecanoic acid; 2) separating the oil phase containing the 3-hydroxydecanoic acid from the reaction system, and carrying out deep hydrolysis reaction under the catalysis of acid to generate the 3-hydroxydecanoic acid. The method can prepare the 3-hydroxydecanoic acid with high yield and high purity.
Description
Technical Field
The invention belongs to the field of organic chemistry, and particularly relates to a preparation method of 3-hydroxydecanoic acid.
Background
With more and more attention paid to environmental protection, degradable materials become a trend of new material development. The polyhydroxy fatty acid is used as a high-performance polymer, is biodegradable, is derived from organisms, and belongs to a material with a full life cycle and environment friendliness. The 3-hydroxydecanoic acid can be used as a monomer of biological material Polyhydroxyalkanoates (PHA), and can be polymerized or copolymerized with other hydroxyfatty acids such as 3-hydroxybutyric acid or 3-hydroxyhexanoic acid, so that the polyhydroxyalkanoates with excellent performance and commercial prospect can be obtained. In addition, the 3-hydroxydecanoate is proved to have the functions of bacteriostasis, inhibition of pollen growth, seed germination and the like, and is applied to the aspect of crop protection.
At present, the source of the 3-hydroxydecanoic acid mainly comprises PHA which is obtained by degrading polyhydroxyalkanoate containing the 3-hydroxydecanoic acid to obtain a monomer, or 3-hydroxydecanoic acid is obtained by hydrolyzing a chemical containing the 3-hydroxydecanoic acid, such as rhamnolipid, or is directly prepared by a fermentation method.
Chinese patent CN108587989 provides a strain for producing 3-hydroxydecanoate and a production method thereof, wherein the strain is pseudomonas aeruginosa, the rhamnosyl transferase I (rh IB) of the strain is inactivated, and the rh IA gene of the strain is utilized to catalyze 3-hydroxyfatty acid dimer (HAA, 3- (3-hydroxyakanoyloxy) alkanoate) synthesized from 3-hydroxyester acyl-CoA/ACP. The engineering strain provided by the invention is fermented and cultured by a culture medium which comprises palm oil and/or glycerol as a carbon source, and the 3-hydroxydecanoate can be obtained after alkaline hydrolysis treatment.
Chinese patent CN1379110 also provides a preparation method of 3-hydroxydecanoate, the scheme of the invention is to ferment and culture recombinant microorganism strains containing gene phaG to obtain the 3-hydroxydecanoate. Firstly, cloning gene phaG into plasmid to construct new plasmid, then transferring the constructed plasmid into bacterial strain to construct DNA recombinant bacterial strain, and obtaining 3-hydroxydecanoate by culturing the recombinant bacterial strain.
U.S. Pat. No. 4, 4,933,281 also mentions a method for preparing 3-hydroxydecanoic acid, which employs a method of hydrolyzing rhamnolipid to obtain rhamnose and co-produce 3-hydroxydecanoic acid.
From the prior preparation technology of 3-hydroxydecanoate, the problems of low yield and low production efficiency exist in the direct fermentation method for producing the 3-hydroxydecanoate, and the separation and purification difficulty of the 3-hydroxydecanoate from the fermentation liquor is large. The method for obtaining 3-hydroxydecanoate by hydrolysis of rhamnolipid is a feasible way, but the prior art has less description.
Rhamnolipids are compounds having the following structure:
wherein R is1Is H or:
wherein R is2Is H or:
CH[(CH2)6CH3]CH2COOH
the 3-hydroxydecanoic acid is a structure contained in rhamnolipid, and different rhamnolipid structures contain 3-hydroxydecanoic acid in different proportions:
defining: 3-hydroxydecanoic acid structure average mass fraction ═ Σ xi*mi
Wherein x isiThe i-th structure rhamnolipid accounts for the mass fraction of all rhamnolipids; m isiIs the proportion of the molecular weight of the 3-hydroxydecanoate structure in the rhamnolipid with the i-th structure to the overall molecular weight of the rhamnolipid.
The hydrolysis of rhamnolipids to rhamnose and 3-hydroxydecanoic acid is as follows:
although the hydrolysis preparation of 3-hydroxydecanoic acid from rhamnolipids is chemically feasible, it was found in the actual preparation process that the hydrolysis preparation of 3-hydroxydecanoic acid from rhamnolipids presents the following problems:
1) the 3-hydroxydecanoate product contains two 3-hydroxydecanoate polymerization product (dimer) impurities of which rhamnolipid is not completely hydrolyzed, and the existence of the impurities reduces the purity of the 3-hydroxydecanoate product on one hand and reduces the yield of 3-hydroxydecanoate prepared by hydrolyzing the rhamnolipid on the other hand.
2) Hydroxyl in the hydrolysate 3-hydroxydecanoate and hydroxyl on rhamnose can generate etherification reaction, and the generated ether bond is difficult to be hydrolyzed again, so that the yield of rhamnose and 3-hydroxydecanoate prepared by rhamnolipid hydrolysis is reduced. The structure shown in the following chemical formula is one of ethers, a rhamnose structure contains 4 hydroxyl groups, and each hydroxyl group can generate etherification reaction with the hydroxyl group of 3-hydroxydecanoic acid to generate an etherification product.
The yield of 3-hydroxydecanoic acid prepared by hydrolyzing rhamnolipid is low due to the reasons, and the purity of the obtained 3-hydroxydecanoic acid is poor, so that the high-end application of the 3-hydroxydecanoic acid is limited.
Disclosure of Invention
In order to overcome the defects of the prior art, the invention provides a method for preparing 3-hydroxydecanoate by efficiently hydrolyzing rhamnolipid with great industrial prospect, and 3-hydroxydecanoate can be prepared with high yield and high purity.
In order to solve the technical problems, the technical scheme adopted by the invention is as follows:
a method of preparing 3-hydroxydecanoic acid from rhamnolipid hydrolysis, the method comprising:
1) the rhamnolipid aqueous solution is subjected to hydrolysis reaction at a certain temperature under the catalysis of acid to generate rhamnose and 3-hydroxydecanoate; 3-hydroxydecanoic acid is in oil phase, rhamnose is in water phase, and unreacted rhamnolipid is in the lowest precipitation phase;
2) separating the oil phase containing the 3-hydroxydecanoate from the reaction system, reacting with a certain amount of acid, and carrying out deep hydrolysis reaction at a certain temperature to generate the 3-hydroxydecanoate.
The rhamnolipids sold in the market are usually derived from fermentation processes, the products usually contain proteins and/or polypeptides, and the impurities are hydrolyzed in a hydrolysis process to generate amino acids, polypeptides and the like. In the research process, the inventor finds that amino acid, polypeptide and the like can generate browning reaction with rhamnose, and the browning reaction product and 3-hydroxydecanoic acid are difficult to separate by the conventional method.
According to the method, the rhamnolipid raw material needs to control the contents of protein, polypeptide, oligopeptide and amino acid. The content of protein in the impurities is not more than 0.1% of the weight of rhamnolipid, and the sum of protein, polypeptide, oligopeptide and amino acid in the rhamnolipid raw material is preferably 0.01-0.1% of the weight of rhamnolipid. The content of protein, polypeptide, oligopeptide and amino acid is usually tested by Coomassie Brilliant blue method, and the content of total protein is used to represent the content of protein, polypeptide, oligopeptide and amino acid in the sample.
Generally, organic membranes with different pore diameters can be used for intercepting proteins, polypeptides and the like with different molecular weights, for example, a nanofiltration membrane with the diameter of 1-10nm is adopted, so that the polypeptides, the proteins and the like can be separated; the protein and the target product may be separated from each other by using the difference in solubility between the protein and the target product in two phases, such as extraction. The protein, the polypeptide, the oligopeptide and the amino acid are thoroughly separated from the rhamnolipid, so that the loss of the rhamnolipid in the separation process is overlarge; in the research process, when the content is controlled below 0.01%, the browning reaction is not obvious, the production cost is higher, and the economical efficiency is poor.
According to the method, the rhamnolipid in the rhamnolipid aqueous solution has a mass fraction of 5% -40%, preferably 7.5% -25%.
According to the method, the acid added in the rhamnolipid hydrolysis process is inorganic acid such as sulfuric acid, phosphoric acid or hydrochloric acid, and can also be organic acid such as naphthalene sulfonic acid and p-toluenesulfonic acid. Preferably one or more of sulphuric acid, phosphoric acid and hydrochloric acid.
According to the method of the present invention, the reaction temperature of the rhamnolipid hydrolysis step in step 1) is 100 ℃ to 150 ℃, preferably 120 ℃ to 140 ℃.
According to the method of the present invention, the amount of acid added in the rhamnolipid hydrolysis step in step 1) (if the acid is an aqueous solution, the amount of acid refers to the mass of solute) is about 0.5% -5%, preferably 1% -2% of the mass of rhamnolipid solution, and preferably the acid is concentrated sulfuric acid with a concentration of 98% or concentrated phosphoric acid with a concentration of 85%.
According to the method of the present invention, the reaction time of the rhamnolipid hydrolysis step in step 1) is 1-10h, preferably 2-4 h.
According to the method, the rhamnolipid is subjected to hydrolysis reaction, an oil phase containing 3-hydroxydecanoate is generated, and the oil phase is separated for further deep hydrolysis by a phase separation method before the mass of the oil phase accounts for 0.5% of the mass of the rhamnolipid aqueous solution raw material. Preferably, the oil phase is separated before the mass of the oil phase reaches 0.1% of the mass of the rhamnolipid aqueous solution raw material. The 3-hydroxy decanoic acid generated by the reaction is transferred away in time to prevent the further reaction; in the experimental process, researchers surprisingly find that when the mass of the oil phase accounts for more than 0.5 percent of that of the rhamnolipid aqueous solution raw material, the dimerization reaction and etherification reaction of the 3-hydroxydecanoate are increased, and the yield of the product is reduced.
According to the method of the invention, the acid added in the deep hydrolysis process of the oil phase containing the 3-hydroxydecanoic acid in the step 2) is inorganic acid such as sulfuric acid, phosphoric acid or hydrochloric acid, and can also be organic acid such as naphthalenesulfonic acid and p-toluenesulfonic acid. Preferably one or more of sulphuric acid, phosphoric acid and hydrochloric acid.
According to the process of the invention, the reaction temperature in the step of deep hydrolysis of the oil phase in step 2) is from 140 ℃ to 180 ℃, preferably from 150 ℃ to 170 ℃.
According to the process of the invention, the acid is added in the step of deep hydrolysis of the oil phase in step 2) in an amount of about 1% to about 5%, preferably about 2% to about 4% of the mass of the oil phase.
According to the method of the present invention, the reaction time of the rhamnolipid hydrolysis step in step 2) is 0.5-5h, preferably 1-2 h.
By adopting the technology of the invention, the positive effects are as follows:
1) by the method of separating the oil phase containing the 3-hydroxydecanoate in time in the hydrolysis reaction process of the rhamnolipid, the probability of etherification reaction between the hydroxyl of the 3-hydroxydecanoate and the hydroxyl of the rhamnose is reduced, and the yield of the rhamnose and the 3-hydroxydecanoate in the hydrolysis process is improved.
2) Deeply hydrolyzing an oil phase obtained by hydrolyzing the rhamnolipid, so that a dimer of the 3-hydroxydecanoic acid which is difficult to separate from the 3-hydroxydecanoic acid can be further hydrolyzed into the 3-hydroxydecanoic acid, thereby improving the yield of the 3-hydroxydecanoic acid and simultaneously improving the purity of the 3-hydroxydecanoic acid.
3) The inventor finds that protein, oligopeptide, polypeptide and amino acid impurities can perform browning reaction with reaction products such as rhamnose and the like in the hydrolysis process to generate dark substances, and the generation of the reaction products reduces the quality yield of the rhamnose in the reaction process on one hand, and on the other hand, the inventor finds that the color number of the 3-hydroxydecanoic acid cannot be improved by a conventional means in the research process. The invention can keep the color number of the 3-hydroxydecanoate product generated by the reaction at a lower level and have lighter color by controlling the content of impurities such as protein, oligopeptide, polypeptide, amino acid and the like in the rhamnolipid raw material.
Description of the drawings:
FIG. 1 is a schematic diagram of the reaction scheme of the example; wherein 1, rhamnolipid solution is fed; 2. a rhamnolipid hydrolysis acid feed; 3. a rhamnolipid hydrolysis reactor; 4. rhamnolipid hydrolysis reaction liquid; 5. a first oil-water separator; 6, rhamnolipid hydrolysis water phase; 7. a rhamnolipid hydrolysis oil phase; 8. deeply hydrolyzing an acid feed by using an oil phase; 9. an oil phase deep hydrolysis reactor; 10. deeply hydrolyzing the reaction solution; 11. a second oil-water separator; 12.3-hydroxydecanoic acid crude product; deep hydrolysis of the aqueous phase.
Detailed Description
The invention will now be further illustrated by the following examples, but is not limited thereto.
The analysis method comprises the following steps:
the analysis of the reaction mass in the process provided by the invention was carried out using ultra high performance liquid tandem triple quadrupole mass spectrometry (Xevo-TQD) as follows:
a chromatographic column: ACQUITY UPLC BEH Amide (1.7 μm, 3.0X 150 mm);
column temperature: 35 ℃;
flow rate: 0.3ml/min
Mobile phase and gradient: a is 0.1% ammonia water; b: acetonitrile;
0min-90％B，4min-50％B，7min-50％B，7.1min-90％B，12min-90％B
an ionization mode: electrospray ionization, negative ion mode;
the detection mode is as follows: multiple Reaction Monitoring (MRM)
Electrospray voltage: 2.8kv
Ion source temperature: 150 ℃ C
Temperature and flow rate of atomizing gas: 400 ℃ and 600L/h
And (3) quantitative ion pair: 163.06/102.97; taper hole voltage 16v and collision voltage 6v
And (3) qualitative ion pair: 163.06/59 (88.98); cone voltage 16v, impact voltage 6 v.
The rhamnolipid concentration is determined by adopting an anthrone sulfuric acid method, the protein content is determined by adopting a Coomassie brilliant blue method, and the polypeptide, the oligopeptide and the amino acid are converted into the content of the protein.
And (3) rhamnolipid purification:
the rhamnolipids sold on the market contain a large amount of protein (protein, polypeptide, oligopeptide, amino acid) impurities because the rhamnolipids are products obtained by fermentation. The proteins in rhamnolipids can be isolated by, but not limited to, the following methods. For example, 500g of crude rhamnolipid product with a rhamnolipid content of 30 wt% and a protein, polypeptide, oligopeptide and amino acid content of 15% produced by lake Zijin Biotechnology Ltd is dissolved in 1000g of deionized water, the pH is adjusted to 2.5, 300g of rhamnolipid-containing precipitate is obtained, the rhamnolipid content is 47.5% by adopting an anthrone sulfuric acid method, and the total content of the protein, polypeptide, oligopeptide and amino acid is 5% by adopting a Coomassie brilliant blue method. And extracting the obtained rhamnolipid precipitate with 2000g ethyl acetate to obtain an ethyl acetate solution containing rhamnolipid, and removing ethyl acetate by distillation to obtain 135g of rhamnolipid product with rhamnolipid content of 95%, wherein the total content of protein, polypeptide, oligopeptide and amino acid is 0.075%. Repeating the above extraction for 1 time to obtain rhamnolipid product with content of about 95%, and total content of protein, polypeptide, oligopeptide, and amino acid of 0.05%. Repeating the extraction for 2 times to obtain rhamnolipid product with content of about 95%, and total content of protein, polypeptide, oligopeptide, and amino acid of 0.035%.
Example 1
500g of rhamnolipid aqueous solution obtained by diluting the above purified rhamnolipid with deionized water was added to a reactor 3(1L) shown in FIG. 1, the concentration of rhamnolipid was 7.5 wt%, and the sum of protein, polypeptide, amino acid, etc. was 0.05 wt% of the rhamnolipid. 7.5g of concentrated sulfuric acid with a concentration of 98% are added and stirred to 500 rpm. The temperature in the kettle was raised to 140 ℃ by means of an external heater. And (3) extracting a stream 4 at the beginning of the reaction, wherein the extraction rate of the stream 4 is 100ml/min, and controlling the oil phase content in the reaction system by controlling the velocity of the circulating stream. And (3) separating the oil phase containing the 3-hydroxydecanoic acid and the water phase containing the rhamnose, which are generated by the reaction, by a first oil-water separator 5, returning the water phase to the reactor 3, and weighing the oil phase content in the extracted stream 4 in the reaction process to be about 0.05 wt%. The reaction was carried out for a total of 3 hours, and 18.0g of the oil phase was collected and analyzed by liquid chromatography external standard, wherein the content of 3-hydroxydecanoic acid was 81%.
18.0g of the oil phase obtained by the hydrolysis is added into a deep hydrolysis reactor 9, 0.5g of concentrated phosphoric acid with the concentration of 85 wt% is added, the stirring speed is 500 r/min, the temperature is raised to 170 ℃, and the reaction is carried out for 1 hour. After the reaction, 15.4g of oil phase is collected, and the content of the 3-hydroxydecanoic acid is 95.4 percent by the analysis of a liquid chromatography external standard.
The color number of the platinum and the cobalt of the 3-hydroxydecanoate is analyzed to be 50 (GB/T3143-1982).
The rhamnolipid adopted in the reaction is a mixture of a plurality of rhamnolipid structures, and the average mass fraction of the 3-hydroxydecanoate structure is 40% through external standard analysis of liquid chromatography.
The yield of 3-hydroxydecanoic acid was 98.1% of the theoretical yield.
Example 2
500g of rhamnolipid aqueous solution diluted with deionized water was added to a reactor 3(1L) shown in FIG. 1, the rhamnolipid concentration was detected to be 15%, and the total amount of proteins, polypeptides, amino acids, etc. was 0.035% of the amount of rhamnolipid. 10g of 85% concentrated sulfuric acid was added thereto, and the mixture was stirred to 500 rpm. The temperature in the kettle was raised to 130 ℃ by means of an external heater. The extraction rate of the stream 4 is 75ml/min, the oil phase containing 3-hydroxydecanoate and the water phase containing rhamnose, which are generated by the reaction, are separated by the first oil-water phase separator 5, the water phase is returned to the reactor 3, and the content of the oil in the stream 4 is detected to be 0.045 wt% in the reaction process. The reaction was carried out for a total of 3 hours, and 36.0g of oil phase was collected and analyzed by liquid chromatography external standard, wherein the content of 3-hydroxydecanoic acid was 76%.
Adding 36.0g of the oil phase obtained by hydrolysis into a deep hydrolysis reactor 9, adding 1.4g of 98% concentrated sulfuric acid, stirring at 500 rpm, heating to 150 ℃, and reacting for 1.5 hours. 30.4g of oil phase is collected after the reaction is finished, and the content of the 3-hydroxydecanoic acid is 96.1 percent by the analysis of a liquid chromatography external standard. The color number of the platinum cobalt of the 3-hydroxydecanoic acid was analyzed to be 45.
The rhamnolipid adopted in the reaction is a mixture of a plurality of rhamnolipid structures, and the average mass fraction of the 3-hydroxydecanoate structure is 40% through external standard analysis of liquid chromatography.
The yield of 3-hydroxydecanoic acid was 97.5% of theory.
Example 3
500g of an aqueous solution of rhamnolipid diluted with deionized water was added to a reactor 3(1L) as shown in the figure, the concentration of rhamnolipid was 25%, and the total amount of protein, polypeptide, amino acid, etc. was 0.075% of the rhamnolipid. 10g of concentrated hydrochloric acid having a concentration of 36.5% are added and stirred to 500 rpm. The temperature in the kettle was raised to 120 ℃ by an external heater. The extraction rate of the stream 4 is 50ml/min, the oil phase containing 3-hydroxydecanoic acid and the water phase containing rhamnose which are generated by the reaction are separated by an oil-water phase separator 5, the water phase is returned to the reaction kettle 3, and the content of the oil in the stream 4 is detected to be about 0.1 wt% in the reaction process. The reaction was carried out for a total of 4 hours, and 60.0g of the oil phase was collected and analyzed by liquid chromatography external standard, wherein the content of 3-hydroxydecanoic acid was 84%.
60.0g of the oil phase obtained by the hydrolysis is added into a deep hydrolysis reactor 9, 1.8g of concentrated hydrochloric acid with the concentration of 36.5 percent is added, the stirring speed is 500 r/min, the temperature is raised to 160 ℃, and the reaction is carried out for 2 hours. 51.5g of oil phase is collected after the reaction is finished, and the oil phase is analyzed by a liquid chromatography external standard, wherein the content of the 3-hydroxydecanoic acid is 94.3 percent, and the platinum-cobalt color number of the 3-hydroxydecanoic acid is 55.
The rhamnolipid adopted in the reaction is a mixture of a plurality of rhamnolipid structures, and the average mass fraction of the 3-hydroxydecanoate structure is 40% through external standard analysis of liquid chromatography.
The yield of 3-hydroxydecanoic acid was 97.1% of theory.
Example 4
500g of rhamnolipid aqueous solution diluted by deionized water is added into a reactor 3(1L) shown in the attached figure, the concentration of rhamnolipid is detected to be 7.5%, and the total amount of protein, polypeptide, amino acid and the like accounts for 0.075% of the mass of rhamnolipid. 7.5g of concentrated sulfuric acid with a concentration of 98% are added and stirred to 500 rpm. The temperature in the kettle was raised to 140 ℃ by an external heater. The extraction rate of the stream 4 is 100ml/min, the oil phase containing 3-hydroxydecanoic acid and the water phase containing rhamnose which are generated by the reaction are separated by an oil-water phase separator 5, the water phase is returned to the reaction kettle 3, and the content of the oil in the stream 4 is detected to be about 0.05 wt% in the reaction process. The reaction was carried out for a total of 3 hours, and 17.9g of oil phase was collected and analyzed by liquid chromatography external standard, wherein the content of 3-hydroxydecanoic acid was 82%.
Adding 17.9g of the oil phase obtained by hydrolysis into a deep hydrolysis reactor 9, adding 0.5g of concentrated phosphoric acid with the concentration of 85 percent, stirring at the rotating speed of 500 revolutions per minute, heating to 170 ℃, and reacting for 1 hour. 15.4g of oil phase is collected after the reaction is finished, and the content of the 3-hydroxydecanoic acid is 95.5 percent by the analysis of a liquid chromatography external standard. The color number of the platinum cobalt for analyzing the 3-hydroxydecanoic acid is 60. The rhamnolipid adopted in the reaction is a mixture of a plurality of rhamnolipid structures, and the average mass fraction of the 3-hydroxydecanoate structure is 40% through liquid chromatography external standard analysis.
The yield of 3-hydroxydecanoic acid was 97.8% of theory.
Comparative example 1
500g of rhamnolipid aqueous solution diluted with deionized water was added to a reactor 3(1L) shown in FIG. 1, and the concentration of rhamnolipid was detected to be 7.5%, and the total amount of protein, polypeptide, amino acid, etc. was 0.05% of the amount of rhamnolipid. 7.5g of concentrated sulfuric acid with a concentration of 98% are added and stirred to 500 rpm. The temperature in the kettle was raised to 140 ℃ by means of an external heater. The reaction was carried out for a total of 3 hours and 18.5g of oil phase was collected and analyzed by liquid chromatography external standard to have a 3-hydroxydecanoic acid content of 65%. The rhamnolipid adopted in the reaction is a mixture of a plurality of rhamnolipid structures, and the average mass fraction of the 3-hydroxydecanoate structure is 40% through liquid chromatography external standard analysis. The color number of the platinum cobalt of the 3-hydroxydecanoic acid was analyzed to be 75. The yield of 3-hydroxydecanoic acid was 80.2%.
Example 5
500g of rhamnolipid aqueous solution diluted with deionized water was added to a reactor 3(1L) shown in FIG. 1, the rhamnolipid concentration was 7.5%, and the sum of proteins, polypeptides, amino acids, etc. was 0.5% of the amount of rhamnolipid. 7.5g of concentrated sulfuric acid with a concentration of 98% are added and stirred to 500 rpm. The temperature in the kettle was raised to 140 ℃ by means of an external heater. The extraction rate of the stream 4 is 100ml/min, the oil phase containing 3-hydroxydecanoic acid and the water phase containing rhamnose which are generated by the reaction are separated by an oil-water phase separator 5, the water phase is returned to the reaction kettle 3, and the content of the oil in the stream 4 is detected to be about 0.05 wt% in the reaction process. The reaction was carried out for a total of 3 hours, and 18.8g of the oil phase was collected and analyzed by liquid chromatography external standard, wherein the content of 3-hydroxydecanoic acid was 82%.
Adding 18.8g of the oil phase obtained by hydrolysis into a deep hydrolysis reactor 9, adding 0.6g of concentrated phosphoric acid with the concentration of 85 percent, stirring at the rotating speed of 500 revolutions per minute, heating to 170 ℃, and reacting for 1 hour. 15.3g of oil phase is collected after the reaction is finished, and the content of the 3-hydroxydecanoic acid is 95.6 percent by the analysis of a liquid chromatography external standard. The color number of the platinum and the cobalt of the 3-hydroxydecanoic acid is analyzed to be 450.
The rhamnolipid adopted in the reaction is a mixture of a plurality of rhamnolipid structures, and the average mass fraction of the 3-hydroxydecanoate structure is 40% through external standard analysis of liquid chromatography.
The yield of 3-hydroxydecanoic acid was 97.6% of theory.
Example 6
500g of rhamnolipid aqueous solution diluted with deionized water was added to a reactor 3(1L) shown in FIG. 1, and the concentration of rhamnolipid was detected to be 7.5%, and the total amount of protein, polypeptide, amino acid, etc. was 0.05% of the amount of rhamnolipid. 7.5g of concentrated sulfuric acid with a concentration of 98% are added and stirred to 500 rpm. The temperature in the kettle was raised to 140 ℃ by means of an external heater. The extraction rate of the stream 4 is 100ml/min, the oil phase containing 3-hydroxydecanoic acid and the water phase containing rhamnose which are generated by the reaction are separated by an oil-water phase separator 5, the water phase returns to the reaction kettle 3, and the content of the oil in the stream 4 is detected to be about 1 wt% in the reaction process. The reaction was carried out for a total of 3 hours and 17.3g of oil phase was collected and analyzed by liquid chromatography external standard to show that the 3-hydroxydecanoic acid content was 65%.
Adding 17.3g of the oil phase obtained by hydrolysis into a deep hydrolysis reactor 9, adding 0.5g of concentrated phosphoric acid with the concentration of 85 percent, stirring at the rotating speed of 500 revolutions per minute, heating to 170 ℃, and reacting for 1 hour. 13.3g of oil phase is collected after the reaction is finished, and the content of the 3-hydroxydecanoic acid is 85.0 percent by the analysis of external standard of liquid chromatography. The color number of the platinum cobalt for analyzing the 3-hydroxydecanoic acid is 60.
The rhamnolipid adopted in the reaction is a mixture of a plurality of rhamnolipid structures, and the average mass fraction of the 3-hydroxydecanoate structure is 40% through external standard analysis of liquid chromatography.
The yield of 3-hydroxydecanoic acid was 75.5% of theory.
Claims (10)
1. A method for preparing 3-hydroxydecanoic acid by hydrolysis of rhamnolipids, comprising:
1) the rhamnolipid aqueous solution is subjected to hydrolysis reaction under the catalysis of acid to obtain a water phase containing rhamnose and an oil phase containing 3-hydroxydecanoic acid;
2) separating the oil phase containing the 3-hydroxydecanoic acid from the reaction system, and carrying out deep hydrolysis reaction under the catalysis of acid to generate the 3-hydroxydecanoic acid.
2. The method according to claim 1, wherein the sum of the proteins, polypeptides, oligopeptides and amino acids in the rhamnolipid material is not more than 0.1% by mass of the rhamnolipid, preferably the sum of the proteins, polypeptides, oligopeptides and amino acids in the rhamnolipid material is 0.01-0.1% by mass of the rhamnolipid.
3. The method according to claim 1, wherein the rhamnolipid is present in the aqueous rhamnolipid solution in a mass fraction of 5% to 40%, preferably 7.5% to 25%.
4. The method according to claim 1, wherein the acid in steps) 1 and 2) is one or more of sulfuric acid, phosphoric acid, hydrochloric acid, naphthalenesulfonic acid, and p-toluenesulfonic acid, preferably one or more of sulfuric acid, phosphoric acid, and hydrochloric acid.
5. The method according to claim 1 or 4, wherein the acid is added in step 1) in an amount of 0.5% to 5%, preferably 1% to 2% by mass of the rhamnolipid solution.
6. The method according to claim 1, wherein the reaction temperature of the rhamnolipid hydrolysis step in step 1) is 100 ℃ to 150 ℃, preferably 120 ℃ to 140 ℃; the hydrolysis reaction time is 1-10h, preferably 2-4 h.
7. The method according to any one of claims 1 to 6, wherein the rhamnolipid is hydrolyzed in step 1) to produce an oil phase containing 3-hydroxydecanoic acid, and step 2) is performed before the oil phase accounts for 0.5% of the mass of the rhamnolipid aqueous solution raw material, preferably before the oil phase reaches 0.1% of the mass of the rhamnolipid aqueous solution raw material.
8. The method according to claim 7, wherein the reaction temperature of the deep oil phase hydrolysis step in the step 2) is 140 ℃ to 180 ℃, preferably 150 ℃ to 170 ℃.
9. The method according to claim 8, wherein the amount of acid added in the step 2) of deep oil phase hydrolysis is 1% to 5%, preferably 2% to 4% of the mass of the oil phase.
10. The process according to claim 9, wherein the hydrolysis reaction time in step 2) is 0.5 to 5 hours, preferably 1 to 2 hours.
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| US4933281A (en) * | 1987-03-17 | 1990-06-12 | The University Of Iowa Research Foundation | Method for producing rhamnose |
| US5501966A (en) * | 1992-06-25 | 1996-03-26 | Hoechst Aktiengesellschaft | Pseudomonas aeruginosa and its use in a process for the biotechnological preparation of L-rhamnose |
| WO2000029604A1 (en) * | 1998-11-18 | 2000-05-25 | The University Of Akron | Production of biological materials by simultaneous aerobic and anaerobic respiration |
| CN108587989A (en) * | 2018-03-21 | 2018-09-28 | 中国科学院微生物研究所 | A kind of bacterial strain and production method for producing 3- hydroxydecanoic acids |
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Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US4933281A (en) * | 1987-03-17 | 1990-06-12 | The University Of Iowa Research Foundation | Method for producing rhamnose |
| US5501966A (en) * | 1992-06-25 | 1996-03-26 | Hoechst Aktiengesellschaft | Pseudomonas aeruginosa and its use in a process for the biotechnological preparation of L-rhamnose |
| WO2000029604A1 (en) * | 1998-11-18 | 2000-05-25 | The University Of Akron | Production of biological materials by simultaneous aerobic and anaerobic respiration |
| CN108587989A (en) * | 2018-03-21 | 2018-09-28 | 中国科学院微生物研究所 | A kind of bacterial strain and production method for producing 3- hydroxydecanoic acids |
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