EP4308534A1 - Process for the purification of vanillin or a vanillin derivative obtained by a biotechnological process - Google Patents
Process for the purification of vanillin or a vanillin derivative obtained by a biotechnological processInfo
- Publication number
- EP4308534A1 EP4308534A1 EP22714200.7A EP22714200A EP4308534A1 EP 4308534 A1 EP4308534 A1 EP 4308534A1 EP 22714200 A EP22714200 A EP 22714200A EP 4308534 A1 EP4308534 A1 EP 4308534A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- vanillin
- derivatives
- equal
- crystallization
- liquid
- 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.)
- Pending
Links
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 title claims abstract description 171
- FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 title claims abstract description 168
- 235000012141 vanillin Nutrition 0.000 title claims abstract description 168
- 238000000034 method Methods 0.000 title claims abstract description 59
- 230000008569 process Effects 0.000 title claims abstract description 42
- 238000000746 purification Methods 0.000 title claims abstract description 20
- 238000011138 biotechnological process Methods 0.000 title claims abstract description 18
- 238000002425 crystallisation Methods 0.000 claims abstract description 33
- 230000008025 crystallization Effects 0.000 claims abstract description 33
- ZENOXNGFMSCLLL-UHFFFAOYSA-N vanillyl alcohol Chemical compound COC1=CC(CO)=CC=C1O ZENOXNGFMSCLLL-UHFFFAOYSA-N 0.000 claims abstract description 29
- 238000000926 separation method Methods 0.000 claims description 43
- 238000000855 fermentation Methods 0.000 claims description 37
- 230000004151 fermentation Effects 0.000 claims description 37
- 239000002028 Biomass Substances 0.000 claims description 35
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 16
- 150000001875 compounds Chemical class 0.000 claims description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 7
- 238000009835 boiling Methods 0.000 claims description 3
- 230000000087 stabilizing effect Effects 0.000 claims description 2
- 239000007788 liquid Substances 0.000 description 43
- 239000000243 solution Substances 0.000 description 24
- 239000003960 organic solvent Substances 0.000 description 21
- 239000002904 solvent Substances 0.000 description 20
- 238000000605 extraction Methods 0.000 description 19
- 239000012074 organic phase Substances 0.000 description 16
- 239000007787 solid Substances 0.000 description 14
- 239000007864 aqueous solution Substances 0.000 description 12
- 238000002360 preparation method Methods 0.000 description 12
- 239000012535 impurity Substances 0.000 description 11
- 239000008346 aqueous phase Substances 0.000 description 10
- 238000001704 evaporation Methods 0.000 description 10
- 238000001728 nano-filtration Methods 0.000 description 10
- 230000006641 stabilisation Effects 0.000 description 10
- 238000011105 stabilization Methods 0.000 description 10
- YQUVCSBJEUQKSH-UHFFFAOYSA-N 3,4-dihydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C(O)=C1 YQUVCSBJEUQKSH-UHFFFAOYSA-N 0.000 description 9
- 230000008020 evaporation Effects 0.000 description 9
- 239000010408 film Substances 0.000 description 9
- 238000001914 filtration Methods 0.000 description 8
- LHGVFZTZFXWLCP-UHFFFAOYSA-N guaiacol Chemical compound COC1=CC=CC=C1O LHGVFZTZFXWLCP-UHFFFAOYSA-N 0.000 description 8
- 238000004821 distillation Methods 0.000 description 7
- KSEBMYQBYZTDHS-HWKANZROSA-N ferulic acid Chemical group COC1=CC(\C=C\C(O)=O)=CC=C1O KSEBMYQBYZTDHS-HWKANZROSA-N 0.000 description 7
- WKOLLVMJNQIZCI-UHFFFAOYSA-N vanillic acid Chemical compound COC1=CC(C(O)=O)=CC=C1O WKOLLVMJNQIZCI-UHFFFAOYSA-N 0.000 description 7
- TUUBOHWZSQXCSW-UHFFFAOYSA-N vanillic acid Natural products COC1=CC(O)=CC(C(O)=O)=C1 TUUBOHWZSQXCSW-UHFFFAOYSA-N 0.000 description 7
- 239000007791 liquid phase Substances 0.000 description 6
- 238000001471 micro-filtration Methods 0.000 description 6
- 238000000108 ultra-filtration Methods 0.000 description 6
- KSEBMYQBYZTDHS-HWKANZROSA-M (E)-Ferulic acid Natural products COC1=CC(\C=C\C([O-])=O)=CC=C1O KSEBMYQBYZTDHS-HWKANZROSA-M 0.000 description 5
- 229940114124 ferulic acid Drugs 0.000 description 5
- KSEBMYQBYZTDHS-UHFFFAOYSA-N ferulic acid Natural products COC1=CC(C=CC(O)=O)=CC=C1O KSEBMYQBYZTDHS-UHFFFAOYSA-N 0.000 description 5
- 235000001785 ferulic acid Nutrition 0.000 description 5
- 244000005700 microbiome Species 0.000 description 5
- QURCVMIEKCOAJU-UHFFFAOYSA-N trans-isoferulic acid Natural products COC1=CC=C(C=CC(O)=O)C=C1O QURCVMIEKCOAJU-UHFFFAOYSA-N 0.000 description 5
- 238000005292 vacuum distillation Methods 0.000 description 5
- RGHHSNMVTDWUBI-UHFFFAOYSA-N 4-hydroxybenzaldehyde Chemical compound OC1=CC=C(C=O)C=C1 RGHHSNMVTDWUBI-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 229960001867 guaiacol Drugs 0.000 description 4
- 239000012528 membrane Substances 0.000 description 4
- 238000001556 precipitation Methods 0.000 description 4
- 238000001223 reverse osmosis Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 230000015556 catabolic process Effects 0.000 description 3
- 238000005520 cutting process Methods 0.000 description 3
- 238000006731 degradation reaction Methods 0.000 description 3
- 238000011026 diafiltration Methods 0.000 description 3
- 239000011552 falling film Substances 0.000 description 3
- 238000000622 liquid--liquid extraction Methods 0.000 description 3
- 238000000638 solvent extraction Methods 0.000 description 3
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- 235000009499 Vanilla fragrans Nutrition 0.000 description 2
- 235000012036 Vanilla tahitensis Nutrition 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000002671 adjuvant Substances 0.000 description 2
- DFYRUELUNQRZTB-UHFFFAOYSA-N apocynin Chemical compound COC1=CC(C(C)=O)=CC=C1O DFYRUELUNQRZTB-UHFFFAOYSA-N 0.000 description 2
- 238000010923 batch production Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000010924 continuous production Methods 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical group COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 229920005610 lignin Polymers 0.000 description 2
- 238000005374 membrane filtration Methods 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 238000005192 partition Methods 0.000 description 2
- 239000012466 permeate Substances 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000007790 solid phase Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 238000002604 ultrasonography Methods 0.000 description 2
- 238000007738 vacuum evaporation Methods 0.000 description 2
- DMEMUWOPWDCEGG-UHFFFAOYSA-N 4-[(4-hydroxy-3-methoxyphenyl)methoxy]-3-methoxybenzaldehyde Chemical compound COc1cc(COc2ccc(C=O)cc2OC)ccc1O DMEMUWOPWDCEGG-UHFFFAOYSA-N 0.000 description 1
- BZQOZUXQDDSNLZ-UHFFFAOYSA-N 4-hydroxy-3-[(4-hydroxy-3-methoxyphenyl)methyl]-5-methoxybenzaldehyde Chemical compound C1=C(O)C(OC)=CC(CC=2C(=C(OC)C=C(C=O)C=2)O)=C1 BZQOZUXQDDSNLZ-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- NPBVQXIMTZKSBA-UHFFFAOYSA-N Chavibetol Natural products COC1=CC=C(CC=C)C=C1O NPBVQXIMTZKSBA-UHFFFAOYSA-N 0.000 description 1
- 239000005770 Eugenol Substances 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- LPRNQMUKVDHCFX-RKQHYHRCSA-N Glucovanillin Chemical compound COC1=CC(C=O)=CC=C1O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 LPRNQMUKVDHCFX-RKQHYHRCSA-N 0.000 description 1
- BJIOGJUNALELMI-ONEGZZNKSA-N Isoeugenol Natural products COC1=CC(\C=C\C)=CC=C1O BJIOGJUNALELMI-ONEGZZNKSA-N 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- UVMRYBDEERADNV-UHFFFAOYSA-N Pseudoeugenol Natural products COC1=CC(C(C)=C)=CC=C1O UVMRYBDEERADNV-UHFFFAOYSA-N 0.000 description 1
- 239000004283 Sodium sorbate Substances 0.000 description 1
- 244000290333 Vanilla fragrans Species 0.000 description 1
- 244000263375 Vanilla tahitensis Species 0.000 description 1
- LPRNQMUKVDHCFX-UHFFFAOYSA-N Vanilloside Natural products COC1=CC(C=O)=CC=C1OC1C(O)C(O)C(O)C(CO)O1 LPRNQMUKVDHCFX-UHFFFAOYSA-N 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 238000010352 biotechnological method Methods 0.000 description 1
- 230000036983 biotransformation Effects 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 235000010244 calcium sorbate Nutrition 0.000 description 1
- 239000004303 calcium sorbate Substances 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- BJIOGJUNALELMI-ARJAWSKDSA-N cis-isoeugenol Chemical compound COC1=CC(\C=C/C)=CC=C1O BJIOGJUNALELMI-ARJAWSKDSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 1
- OPGYRRGJRBEUFK-UHFFFAOYSA-L disodium;diacetate Chemical compound [Na+].[Na+].CC([O-])=O.CC([O-])=O OPGYRRGJRBEUFK-UHFFFAOYSA-L 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229960002217 eugenol Drugs 0.000 description 1
- -1 ferulic acid Chemical class 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 235000021474 generally recognized As safe (food) Nutrition 0.000 description 1
- 235000021473 generally recognized as safe (food ingredients) Nutrition 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 229930182478 glucoside Natural products 0.000 description 1
- 150000008131 glucosides Chemical class 0.000 description 1
- LPRNQMUKVDHCFX-RGDJUOJXSA-N glucovanillin Natural products COC1=CC(C=O)=CC=C1O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 LPRNQMUKVDHCFX-RGDJUOJXSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- JMMWKPVZQRWMSS-UHFFFAOYSA-N isopropanol acetate Natural products CC(C)OC(C)=O JMMWKPVZQRWMSS-UHFFFAOYSA-N 0.000 description 1
- 229940011051 isopropyl acetate Drugs 0.000 description 1
- GWYFCOCPABKNJV-UHFFFAOYSA-M isovalerate Chemical compound CC(C)CC([O-])=O GWYFCOCPABKNJV-UHFFFAOYSA-M 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- DUWWHGPELOTTOE-UHFFFAOYSA-N n-(5-chloro-2,4-dimethoxyphenyl)-3-oxobutanamide Chemical compound COC1=CC(OC)=C(NC(=O)CC(C)=O)C=C1Cl DUWWHGPELOTTOE-UHFFFAOYSA-N 0.000 description 1
- 238000009928 pasteurization Methods 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 235000010241 potassium sorbate Nutrition 0.000 description 1
- 239000004302 potassium sorbate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 230000005588 protonation Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000012465 retentate Substances 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 235000002639 sodium chloride Nutrition 0.000 description 1
- 235000017454 sodium diacetate Nutrition 0.000 description 1
- LROWVYNUWKVTCU-STWYSWDKSA-M sodium sorbate Chemical compound [Na+].C\C=C\C=C\C([O-])=O LROWVYNUWKVTCU-STWYSWDKSA-M 0.000 description 1
- 235000019250 sodium sorbate Nutrition 0.000 description 1
- 230000007928 solubilization Effects 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- BJIOGJUNALELMI-UHFFFAOYSA-N trans-isoeugenol Natural products COC1=CC(C=CC)=CC=C1O BJIOGJUNALELMI-UHFFFAOYSA-N 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
- 235000009529 zinc sulphate Nutrition 0.000 description 1
- 239000011686 zinc sulphate Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/78—Separation; Purification; Stabilisation; Use of additives
- C07C45/81—Separation; Purification; Stabilisation; Use of additives by change in the physical state, e.g. crystallisation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/78—Separation; Purification; Stabilisation; Use of additives
- C07C45/79—Separation; Purification; Stabilisation; Use of additives by solid-liquid treatment; by chemisorption
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/78—Separation; Purification; Stabilisation; Use of additives
- C07C45/80—Separation; Purification; Stabilisation; Use of additives by liquid-liquid treatment
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/24—Preparation of oxygen-containing organic compounds containing a carbonyl group
Definitions
- the present invention relates to a process for purifying vanillin or a vanillin derivative obtained by a biotechnological process.
- Vanillin can be obtained by various methods known to those skilled in the art, and in particular by the following two routes:
- a so-called natural route based on a biotechnological process comprising in particular the culture of a microorganism capable of allowing the biotransformation of a fermentation substrate into vanillin. It is in particular known from application EP0885968 such a process in which the fermentation substrate is ferulic acid. US patent 5017388 describes a process in which the fermentation substrate is eugenol and/or isoeugenol. These processes lead to the preparation of a so-called natural vanillin.
- vanillin can also be prepared according to a method described as "bio-based” in which the vanillin is derived from lignin, mention may be made in particular of documents US 2745796, DE1132113 and the article entitled “Preparation of lignin from wood dust as vanillin source and comparison of different extraction method” by Azadbakht et al in International Journal of Biology and Biotechnology, 2004, vol 1, No 4, pp 535-537.
- natural vanillin can be purified according to the process described in application EP 2791098 which comprises a step of liquid/liquid extraction of impurities having a higher pKa than that of vanillin.
- the yield of this process is good, generally greater than 80%, however in order to obtain improved qualities in terms of organoleptic properties such as the smell and/or the color of the vanillin, several additional purification steps are necessary, thus reducing the overall yield of this process.
- the energy efficiency of this process is also globally degraded due to the use of large quantities of solvents.
- the present invention relates to a process for the purification of vanillin or its derivatives obtained by a biotechnological process comprising at least one step in which the vanillin or its derivatives is separated from the vanillic alcohol or its derivatives.
- Figures 1 to 5 schematize various processes for the purification of vanillin or its derivatives obtained by a biotechnological process according to the present invention.
- the expression “natural vanillin” designates a vanillin obtained by a biotechnological process.
- a process for the preparation of natural vanillin denotes here a biotechnological process comprising the culture of a microorganism capable of allowing the transformation of a fermentation substrate into vanillin.
- the microorganism may be of wild origin or be a genetically modified microorganism (GMM) obtained by molecular biology. Very preferably, it may be a ferulic acid fermentation process, such as that described in patent application EP 0885968.
- vanillin may be produced by a glucose or d protocatechuic acid as described in patent application WO 2013/022881.
- vanillin derivative refers to any compound which may be derived from vanillin and in particular to vanillin in salified form or to glucovanillin.
- the term “derivative of vanillic alcohol” refers to any compound which may derive from vanillic alcohol and in particular to vanillic alcohol in salified form or to the glucoside of vanillic alcohol.
- the term “crystallization” refers to a process in which a substance changes to the solid state by a physical process, such as in particular lowering the temperature.
- the term “precipitation” refers to a process in which a substance passes into the solid state by a chemical transformation, such as in particular by protonation thanks to a change in pH.
- the present invention relates to a process for the purification of vanillin or its derivatives obtained by a biotechnological process comprising at least one step in which the vanillin or its derivatives is separated from the vanillic alcohol or its derivatives.
- the purification process of the present invention comprises at least one step of crystallization of vanillin or its derivatives.
- the crystallization step makes it possible to purify vanillin or its derivatives, obtained by a biotechnological process, having a purity of between 85% and 99%, preferably greater than or equal to 90%, very preferably greater than or equal to 95%.
- the crystallization process makes it possible to produce a vanillin or its purified derivatives having a purity greater than or equal to 95%, preferably greater than or equal to 97%, very preferably greater than or equal to 99%.
- Vanillin having a purity of between 85% and 99% generally comprises at least one other compound chosen from vanillic alcohol, vanillic acid, guaiacol, acetovanillone, 4-((4-hydroxy-3-methoxy-benzyl)oxy)-3 -methoxybenzaldehyde and 4-hydroxy-3-(4-hydroxy-3-methoxybenzyl)-5-methoxybenzaldehyde.
- the vanillic alcohol content is generally between 0.01% and 15% by weight.
- Crystallization is usually carried out in an alcoholic solution.
- the solvent used for the crystallization can be a water-soluble alcohol, preferably ethanol.
- the solvent used for the crystallization can be a water/alcohol mixture.
- the amount of alcohol is between 2% and 40% by weight, preferably between 5% and 35% by weight, and very preferably between 15% and 25% by weight.
- the vanillin concentration, at the start of crystallization is between 5% and 60% by weight, preferably between 10% and 50% by weight, advantageously between 15% and 35% by weight, and even more preferably between 15% and 25%.
- the crystallization allows the separation of the vanillin or its derivatives and the vanillic alcohol or its derivatives, this separation is advantageously carried out without degradation of the vanillin or its derivatives.
- the crystallization allows the separation of the vanillin and the vanillic alcohol, this separation is advantageously carried out without degradation of the vanillin.
- the crystallization is carried out at a temperature comprised between 0°C and 50°C.
- the crystallization yield is generally greater than or equal to 80%.
- the vanillin obtained at the end of the crystallization step generally has a color in 10% by weight ethanolic solution less than or equal to 150 Hazen, preferably less than or equal to 100 Hazen, and very preferably less than or equal to 50 Hazen .
- the present invention relates to a process for the purification of vanillin or its derivatives obtained by a biotechnological process in which the vanillin or its derivatives is separated from the vanillic alcohol or its derivatives.
- the process for purifying vanillin or its derivatives is particularly optimized and makes it possible to reduce the quantity of organic solvent used.
- the amount of organic solvent used in the purification process is reduced by at least 5% compared to purification processes for vanillin obtained by a biotechnological process.
- Solvent reduction is calculated relative to processes using at least one organic solvent.
- the amount of solvent used is calculated from any amount of solvent used for purification between the fermentation broth until the purified, crystallized vanillin is obtained. The process is thus improved by compared to the processes of the state of the art in that it has a reduced ecological and/or environmental impact.
- the present invention relates to a process for the purification of vanillin or its derivatives obtained by a biotechnological process in which the vanillin or its derivatives is separated from the vanillic alcohol or its derivatives.
- the process of the present invention makes it possible to upgrade vanillic alcohol or its derivatives.
- the vanillic alcohol or its derivatives can indeed be recovered in the filtrate resulting from the crystallization.
- this vanillic alcohol or its derivatives can then be upgraded as a synthesis intermediate, in particular for the preparation of organic compounds for the cosmetics or perfumery industry.
- the process of the present invention does not degrade vanillic alcohol or its derivatives.
- the vanillin or its derivatives is in aqueous solution in a fermentation broth.
- the process of the present invention consists in purifying an aqueous solution of vanillin or its derivatives.
- the vanillin concentration in the aqueous solution is between 0.2 and 5% by weight, preferably between 0.8 and 2.5% by weight, very preferably between 1.0 and 1.8% in weight.
- the aqueous solution further comprises: biomass, in general, the amount of biomass is between 0.5 and 5% by weight of dry matter, preferably between 1.0 and 2.0% by weight of dry matter ; vanillic alcohol, in general, the amount of vanillic alcohol is between 0.01% and 0.5% by weight, preferably between 0.05% and 0.3% by weight; vanillic acid, in general, the amount of vanillic acid is between 0.01% and 0.5% by weight, preferably between 0.05% and 0.3% by weight.
- the aqueous solution can also comprise other compounds such as ferulic acid, and derivatives of ferulic acid, coumaric acid, para-hydroxybenzaldehyde, guaiacol. These compounds can be separated from vanillin or its derivatives according to the process of the present invention.
- at least one compound chosen from ferulic acid, ferulic acid derivatives, coumaric acid, para-hydroxybenzaldehyde or guaiacol can be utilized in particular as a synthesis intermediate.
- the purification process of the present invention may comprise at least one step consisting of a separation of the biomass from the aqueous solution of vanillin or its derivatives.
- This stage is a stage of separation of a solid phase: the biomass, from a liquid phase.
- the liquid phase obtained at the end of the biomass separation step is an aqueous phase comprising vanillin or its derivatives.
- the step of separating the biomass can be carried out by filtration such as frontal filtration or tangential filtration, in particular membrane filtration, such as microfiltration, ultrafiltration, nanofiltration, or reverse osmosis.
- Membrane filtration can be carried out in concentration or in diafiltration.
- the biomass separation step is a frontal filtration, it is possible to add adjuvants in order to improve the efficiency of the filtration.
- the biomass separation step can be carried out by one or more microfiltration membranes, in particular having a cutting limit of approximately 0.2 ⁇ m, followed by one or more ultrafiltrations having a limit of smaller cut than microfiltration.
- the vanillin is dissolved in the aqueous phase and the biomass is retained by the membranes.
- ultrafiltration also allows the separation of molecules dissolved in the fermentation broth.
- a solvent preferably water
- the amount of solvent added is between 0.5 and 5 equivalents by volume of fermentation broth.
- the microfiltration, ultrafiltration or diafiltration can be coupled with a nanofiltration or reverse osmosis step.
- nanofiltration makes it possible to increase the vanillin concentration in the retentate from the nanofiltration step while the water passes through the membrane (permeate from the nanofiltration step).
- the permeate from this nanofiltration step can advantageously be recycled.
- reverse osmosis has a cut limit of less than or equal to 100 Da.
- nanofiltration has a cut limit of less than or equal to 400 Da.
- nanofiltration has a cutting limit greater than or equal to 100 Da, for example cutting limit between 100 and 250 Da.
- the fermentation Prior to this step of separating the biomass from the aqueous solution of vanillin or its derivatives, the fermentation must be stabilized.
- stabilization refers to any method making it possible to avoid the degradation, in particular by reduction, of the vanillin or its derivatives between the end of the fermentation and the purification process.
- the stabilization can be carried out by adding at least one compound.
- the compound is preferably chosen from sodium benzoate, ascorbic acid and its salts, potassium, calcium or sodium sorbate, zinc sulphate, propanoic acid, acetic acid or its salts, sodium diacetate.
- the amount of compound added is between 0.2 g/L and 6 g/L.
- the stabilization can be carried out by changing the temperature of the fermentation broth.
- the temperature is controlled so as to reach a temperature between 15°C and 23°C, preferably between 18°C and 21°C.
- the stabilization can be carried out by changing the pH of the fermentation broth.
- the pH is controlled so as to reach a pH less than or equal to 7.5, preferably less than or equal to 7, very preferably less than or equal to 6.8.
- the pH is controlled so as to achieve a pH greater than or equal to 5.0, preferably greater than or equal to 6.
- the fermentation broth can also be pasteurized.
- the fermentation must is then heated to a temperature between 50°C and 90°C, preferably between between 60°C and 80°C.
- the heating is generally maintained for a period comprised between 10 min and 120 min, preferably comprised between 15 min and 45 min, for example for 20 min.
- the fermentation must can be stabilized by ultrasound.
- ultrasound is emitted in the fermentation must for a period of between 10 min and 120 min.
- these aspects can be carried out separately or jointly, thus, by way of nonlimiting example, it is possible to modify the temperature, the pH and to add a compound according to the conditions described above.
- the methods without adding compounds are advantageous, without wishing to be bound by any theory whatsoever, they make it possible to avoid possible deleterious effects on vanillin or its derivatives, in particular in terms of odor or color.
- the purification process generally comprises at least one liquid/liquid extraction step making it possible to recover the vanillin or its derivatives in an organic solution.
- the liquid/liquid extraction step advantageously makes it possible to transfer the vanillin or its derivatives in aqueous solution into the fermentation must or, after a solid/liquid separation of the fermentation must, into an organic phase.
- an organic phase is obtained comprising vanillin or its derivatives.
- the liquid/liquid extraction step advantageously allows the separation of vanillin or its derivatives from compounds that are very soluble in water such as vanillic acid or its derivatives, ferulic acid.
- the pH of the aqueous solution is between 5 and 8, preferably between 5.5 and 7.5, very preferably between 6 and 7.
- the extraction solvent is chosen for these solubilization properties of vanillin or its derivatives, advantageously the solvent can be of biosourced origin.
- the solvent chosen is compatible with the standards of the food industry, in particular FEMA GRAS, immiscible with water.
- the solvent is chosen from methyl ethyl ketone, methyl isobutyl ketone, ethyl acetate, isopropyl acetate or mixtures thereof.
- the liquid/liquid extraction step can be a discontinuous liquid-liquid extraction.
- the volume ratio of solvent relative to the aqueous solution of vanillin or its derivatives is between 1:5 and 5:1, preferably between 1:1 and 5:1, preferably between 1.5:1 and 3:1.
- the liquid/liquid extraction step can be carried out continuously.
- the volume ratio of solvent relative to the aqueous solution of vanillin or its derivatives is between 5:1 and 1:2, preferably between 3:1 and 1:1.
- the yield of vanillin or its derivatives from the liquid/liquid extraction stage is generally greater than or equal to 95%, preferably greater than or equal to 97%, very preferably greater than or equal to 98%.
- the stages of separation of the biomass and of liquid/liquid extraction can be carried out simultaneously. This particular aspect makes it possible to extract the vanillin or its derivatives in the organic solvent from the fermentation broth.
- the biomass is then separated from the two-phase system. This process is advantageous in that the loss of vanillin or its derivatives in the biomass is reduced.
- This separation step can in particular be carried out continuously by centrifugation, in particular by using a two- or three-phase centrifuge or a counter-current extractor.
- the concentration (C) of the organic solution of vanillin or its derivatives obtained at the end of the liquid/liquid extraction step is generally between 0.1% by weight and 10% by weight.
- a stripping step can be carried out on the aqueous stream obtained at the end of the liquid-liquid extraction step.
- the stripping step allows the recovery of organic compounds contained in the aqueous flow, in particular vanillin or its derivatives.
- stripping makes it possible to improve the yield of vanillin or its derivatives.
- the stripping step also makes it possible to facilitate the treatment of the aqueous effluents.
- the method of the present invention comprises at least one step of concentration of an aqueous or organic solution of vanillin or its derivatives.
- the concentration can be carried out on an aqueous solution of vanillin or its derivatives obtained at the end of the stage of separation of the biomass.
- the concentration can be carried out on an organic solution of vanillin or its derivatives obtained after the liquid/liquid extraction.
- the vanillin or its derivatives is in liquid or solid form depending on the temperature.
- at least 95% of the solvent has been separated from the vanillin or its derivatives.
- the concentration step can consist of one or more concentration steps.
- At least 95% of the quantity of solvent present in the organic solution of vanillin or its derivatives obtained at the end of the liquid-liquid extraction can be evaporated.
- the concentration of the organic solution obtained at the end of the liquid/liquid extraction step can be partial, to result in the formation of a solution of vanillin or its concentrated derivatives (Cl), preferably having a higher concentration than the concentration (C) of the organic solution of vanillin or its derivatives obtained at the end of the liquid/liquid extraction step.
- the organic solution of vanillin or its derivatives obtained at the end of the liquid/liquid extraction step is concentrated so as to obtain an organic solution of vanillin or its derivatives (Cl) having a concentration of between 10% by weight and 95% by weight.
- the organic solution of vanillin or its derivatives (Cl) can be subjected to one or more subsequent concentration steps so as to obtain vanillin or its derivatives in liquid or solid form depending on the temperature.
- the concentration step can be carried out in a continuous process or in a batch process.
- the concentration step can be carried out in a stirred reactor or in a distillation column.
- the concentration step is carried out under vacuum, preferably at a pressure between 5 mbar and 300 mbar, preferably between 50 mbar and 250 mbar.
- the concentration step is generally carried out at a temperature between 25°C and 100°C.
- the concentration step can be carried out using tray or packed distillation columns, falling film evaporators, wiped film evaporators or partition columns.
- the concentration step is carried out at a pressure at the distillation head of between 0.5 bar and 5 bar, preferably between 1 bar and 3 bar.
- the temperature at the distillation head is generally between 75°C and 150°C, preferably between 85°C and 120°C and very preferably between 90°C and 110°C.
- the concentration step is carried out so as to reduce the transit time of the vanillin or its derivatives in the reactors or columns.
- the concentration step makes it possible to recover the vanillin or its derivatives at the bottom of the column while the solvent is recovered at the top of the column.
- the vanillin or its derivatives at the bottom of the column generally have a purity greater than or equal to 90%.
- Other compounds are present with vanillin or its derivatives at the bottom of the column, in particular vanillic alcohol or its derivatives.
- the purification process of the present invention may comprise at least one step in which vanillin or its derivatives is separated from compounds having a higher boiling point than that of vanillin or its derivatives.
- This step can be a tar removal step.
- the tar removal step can be carried out in a distillation column, a partition column, a falling film evaporator, or a wiped film evaporator.
- the purification process of the present invention comprises at least one step of crystallization of vanillin or its derivatives as described above.
- the crystallization can in particular be carried out on vanillin or its derivatives obtained after at least one step chosen from liquid/liquid extraction, concentration and tar removal.
- the purification process of the present invention may further comprise a step of precipitation of vanillin or its derivatives in the presence of the biomass.
- This precipitation step is generally preliminary to the biomass separation step.
- the precipitation of vanillin or its derivatives in the presence of biomass is generally carried out at a temperature between 0°C and 6°C.
- This step can be simultaneous with a step for stabilizing the fermentation broth, in particular by modifying the pH. This aspect then allows the separation of the biomass from the liquid phase.
- the vanillin or its derivatives being in solid form is recovered in the cake with the biomass.
- the cake is advantageously taken up with a solvent in which the vanillin or its derivatives is soluble, to allow the formation of a solid phase and an organic phase of vanillin or its liquid derivatives which can be purified according to the different concentration stages, tar removal and/or crystallization as described above.
- the process for purifying vanillin or its derivatives obtained by a biotechnological process is characterized in that no organic solvent is used except for the solvent used during the crystallization.
- the quantity of organic solvent used is reduced by 100% compared to the methods of the state of the art.
- the method for purifying vanillin or its derivatives obtained by a biotechnological method and, prior to the crystallization step, may comprise at least one step of solid/liquid separation, concentration and/or tar removal such as previously described without the use of organic solvent.
- the fermentation broth is subjected to a stabilization step.
- This stabilized fermentation broth is then centrifuged with a plate centrifuge allowing the separation of the biomass.
- An organic solvent is added simultaneously to make it possible to extract the vanillin in organic solution, the aqueous and organic phases are separated.
- the organic phase is then subjected to concentration, preferably using a wiped film evaporator, and/or a falling film evaporator.
- the evaporated organic solvent is recycled to the biomass separation step.
- the vanillin is then subjected to a second stage of evaporation, preferably in a wiped film evaporator so as to separate the vanillin from the heavies.
- the vanillin is recovered at the head of the evaporator with any impurities such as vanillic alcohol. Finally, this stream recovered at the head of the evaporator is crystallized to allow the preparation of a crystallized vanillin having a purity greater than or equal to 99.5% and having a color in ethanolic solution at 10% by weight less than or equal to 150 Hazen, preferably less than or equal to 100 Hazen, and very preferably less than or equal to 50 Hazen.
- the fermentation broth is subjected to a stabilization step.
- This stabilized fermentation must is then decanted, then filtered allowing the separation of the biomass.
- An organic solvent is added simultaneously to make it possible to extract the vanillin in organic solution, the aqueous and organic phases are separated.
- the organic phase is then subjected to concentration by vacuum distillation.
- the evaporated organic solvent can be recycled to the biomass separation step.
- the vanillin is then subjected to a second stage of evaporation, preferably in a wiped film evaporator so as to separate the vanillin and the heavies.
- the vanillin is recovered at the top of the evaporator with any impurities such as vanillic alcohol.
- this stream recovered at the head of the evaporator is crystallized to allow the preparation of a crystallized vanillin having a purity greater than or equal to 99.9% and having a color in ethanolic solution at 10% by weight less than or equal to 150 Hazen, preferably less than or equal to 100 Hazen, and very preferably less than or equal to 50 Hazen.
- the fermentation must is subjected to a stabilization step by lowering the temperature to 21° C., adjusting the pH to 6.8, and adding an adjuvant or a pasteurization at 60°C for 20 min.
- An organic solvent is added simultaneously to allow the vanillin to be extracted in organic solution.
- the separation of the biomass and the aqueous and organic phases is carried out using a counter-current extractor.
- the organic phase is then subjected to concentration by vacuum distillation.
- the evaporated organic solvent can be recycled to the biomass separation step.
- the vanillin is then subjected to a second stage of evaporation, preferably in a wiped film evaporator so as to separate the vanillin and the heavies.
- the vanillin is recovered at the top of the evaporator with any impurities such as vanillic alcohol. Finally, this stream recovered at the top of the evaporator is crystallized to allow the preparation of a crystallized vanillin having a purity greater than or equal to 99.9% and having a color in 10% by weight ethanol solution less than or equal to 150 Hazen, preferably less than or equal to 100 Hazen, and very preferably less than or equal to 50 Hazen.
- the fermentation broth is subjected to a stabilization step.
- This stabilized fermentation broth is stirred with the simultaneous addition of an organic solvent.
- This mixture is then separated using a centrifugal decanter.
- the organic phase is then subjected to concentration by continuous or discontinuous vacuum distillation.
- the evaporated organic solvent can be recycled to the biomass separation step.
- the vanillin is then subjected to a second stage of evaporation, preferably in a wiped film evaporator so as to separate the vanillin and the heavies.
- the vanillin is recovered at the top of the evaporator with any impurities such as vanillic alcohol.
- this stream recovered at the head of the evaporator is crystallized to allow the preparation of a crystallized vanillin having a purity greater than or equal to 99.9% and having a color in ethanolic solution at 10% by weight less than or equal to 150 Hazen, preferably less than or equal to 100 Hazen, and very preferably less than or equal to 50 Hazen.
- the fermentation broth is subjected to a stabilization step.
- This stabilized fermentation must is filtered allowing the separation of the biomass. Filtration is carried out by microfiltration followed by nanofiltration.
- An organic solvent is then added to make it possible to extract the vanillin in organic solution, the aqueous and organic phases are separated by continuous extraction.
- the organic phase is then subjected to concentration by continuous or discontinuous vacuum distillation.
- the evaporated organic solvent can be recycled to the biomass separation step.
- the vanillin is then subjected to a second stage of evaporation, preferably in a wiped film evaporator so as to separate the vanillin and the heavies.
- the vanillin is recovered at the top of the evaporator with any impurities such as vanillic alcohol. Finally, this stream recovered at the head of the evaporator is crystallized to allow the preparation of a crystallized vanillin having a purity greater than or equal to 99.9% and having a color in ethanolic solution at 10% by weight less than or equal to 150 Hazen, preferably less than or equal to 100 Hazen, and very preferably less than or equal to 50 Hazen.
- the fermentation broth is subjected to a stabilization step.
- This stabilized fermentation must is filtered allowing the separation of the biomass by frontal filtration.
- An organic solvent is then added to make it possible to extract the vanillin in organic solution, the aqueous and organic phases are separated by continuous extraction.
- the organic phase is then subjected to concentration by continuous or discontinuous vacuum distillation.
- the evaporated organic solvent can be recycled to the biomass separation step.
- the vanillin is then subjected to a second stage of evaporation, preferably in a wiped film evaporator so as to separate the vanillin and the heavies.
- the vanillin is recovered at the top of the evaporator with any impurities such as vanillic alcohol.
- this stream recovered at the head of the evaporator is crystallized to allow the preparation of a crystallized vanillin having a purity greater than or equal to 99.9% and having a color in ethanolic solution at 10% by weight less than or equal to 150 Hazen, preferably less than or equal to 100 Hazen, and very preferably less than or equal to 50 Hazen.
- the fermentation broth is stabilized and precipitated.
- a solid/liquid separation step is then carried out so as to separate the cake comprising the vanillin and the biomass from a liquid aqueous phase comprising certain impurities of the fermentation process.
- the vanillin contained in the cake is then dissolved with an organic solvent or water to allow the separation of an aqueous or organic liquid phase comprising the vanillin from the biomass.
- the aqueous or organic liquid phase comprising the vanillin is then subjected to steps of concentration, separation of heavy substances and crystallization as described in the first embodiment.
- the fermentation broth is stabilized.
- a solid/liquid separation step is then carried out so as to separate the cake comprising the biomass from a liquid aqueous phase comprising the vanillin.
- the solid/liquid separation can be carried out by any method described according to embodiments 1 to 6.
- the aqueous liquid phase is then subjected to a step of adsorption on resin or pertraction with simultaneous addition of an organic solvent. .
- the organic phase comprising the vanillin is then subjected to steps of concentration, separation of heavy substances and crystallization as described in the first embodiment.
- the fermentation broth is stabilized.
- a solid/liquid separation stage is then carried out so as to separate the biomass, preferably this separation is carried out by microfiltration or diafiltration.
- This first separation can be followed by an ultrafiltration step.
- This ultrafiltration makes it possible in particular to separate particles not separated during the separation on a ceramic membrane.
- the ultrafiltrate is then subjected to a nanofiltration step (or optionally reverse osmosis) in order to concentrate the flux in vanillin.
- This vanillin stream is then subjected to a crystallization step in a water/alcohol solvent as described previously.
- a composition as defined in Table 1 is subjected to crystallization from a water/ethanol mixture, in which the ethanol content is between 15 and 25% by weight. Crystallization is carried out by cooling from 40°C to 4°C. The vanillin concentration at the start of crystallization is between 15 and 25% by weight.
- Crystallized vanillin After crystallization, the crystallized vanillin is filtered, washed with water, dried and analyzed. Crystallized vanillin has a purity of 99.6%. Vanillic alcohol content is 0.04%. The vanillic acid content is 0.01%.
- a composition as defined in Table 1 is subjected to vacuum evaporation.
- the purified vanillin is analyzed.
- Purified vanillin has a purity of 99.7%.
- Vanilla alcohol content is less than 0.01%.
- the vanillic acid content is less than 0.01%.
- Example 2.2 After evaporation, in continuous mode, the purified vanillin is analyzed.
- the overall yield of the vanillin obtained in the context of Example 2.2 is 95%. However, purified vanillin has a purity of 98%.
- the vanilla alcohol content is 1%.
- the vanillic acid content is less than 0.01%.
- the process of the present invention advantageously makes it possible to obtain vanillin having good purity characteristics and with very good yields.
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Abstract
The present invention relates to a process for the purification of vanillin or derivatives thereof obtained by a biotechnological process, which method comprises at least one step in which vanillin or the derivatives thereof are separated from vanillyl alcohol or the derivatives thereof by crystallization.
Description
DESCRIPTION DESCRIPTION
PROCEDE DE PURIFICATION DE VANILLINE OU D'UN DERIVE DE VANILLINE OBTENUS PAR UN PROCEDEMETHOD FOR PURIFYING VANILLIN OR A VANILLIN DERIVATIVE OBTAINED BY A PROCESS
BIOTECHNOLOGIQUE BIOTECHNOLOGY
Domaine de l'invention Field of the invention
La présente invention concerne un procédé de purification de vanilline ou d'un dérivé de vanilline obtenus par un procédé biotechnologique. The present invention relates to a process for purifying vanillin or a vanillin derivative obtained by a biotechnological process.
Art antérieur Prior art
La vanilline peut être obtenue par différentes méthodes connues de l'homme de l'art, et notamment par les deux voies suivantes : Vanillin can be obtained by various methods known to those skilled in the art, and in particular by the following two routes:
- Une voie dite naturelle basée sur un procédé biotechnologique comprenant notamment la culture d'un microorganisme apte à permettre la biotransformation d'un substrat de fermentation en vanilline. Il est notamment connu de la demande EP0885968 un tel procédé dans lequel le substrat de fermentation est l'acide férulique. Le brevet US 5017388 décrit un procédé dans lequel le substrat de fermentation est l'eugénol et/ou l'isoeugénol. Ces procédés aboutissent à la préparation d'une vanilline dite vanilline naturelle. - A so-called natural route based on a biotechnological process comprising in particular the culture of a microorganism capable of allowing the biotransformation of a fermentation substrate into vanillin. It is in particular known from application EP0885968 such a process in which the fermentation substrate is ferulic acid. US patent 5017388 describes a process in which the fermentation substrate is eugenol and/or isoeugenol. These processes lead to the preparation of a so-called natural vanillin.
- Une voie dite synthétique comprenant des réactions chimiques classiques à partir du gaïacol ne faisant pas intervenir de microorganisme. Ce procédé aboutit à la préparation d'une vanilline dite vanilline synthétique. - A so-called synthetic route comprising conventional chemical reactions from guaiacol that do not involve microorganisms. This process leads to the preparation of a so-called synthetic vanillin.
Enfin la vanilline peut également être préparée selon une voie qualifiée de « bio-based » dans laquelle la vanilline est issue de lignine, on peut citer en particulier les documents US 2745796, DE1132113 et l'article intitulé « Préparation of lignin from wood dust as vanillin source and comparison of different extraction method » by Azadbakht et al in International Journal of Biology and Biotechnology, 2004, vol 1, No 4, pp 535-537. Finally, vanillin can also be prepared according to a method described as "bio-based" in which the vanillin is derived from lignin, mention may be made in particular of documents US 2745796, DE1132113 and the article entitled "Preparation of lignin from wood dust as vanillin source and comparison of different extraction method” by Azadbakht et al in International Journal of Biology and Biotechnology, 2004, vol 1, No 4, pp 535-537.
Actuellement la vanilline naturelle peut être purifiée selon le procédé décrit dans la demande EP 2791098 qui comprend une étape d'extraction liquide/liquide d'impuretés ayant un pKa plus élevé que celui de la vanilline. Le rendement de ce procédé est bon, en général supérieur à 80%, toutefois afin d'obtenir des qualités améliorées quant aux propriétés organoleptiques telles que l'odeur et/ou la couleur de la vanilline plusieurs étapes de purification additionnelles sont nécessaires faisant ainsi chuter le rendement global de ce procédé. L'efficacité énergétique de ce procédé est également globalement dégradée du fait de l'utilisation de grandes quantités de solvants. Currently, natural vanillin can be purified according to the process described in application EP 2791098 which comprises a step of liquid/liquid extraction of impurities having a higher pKa than that of vanillin. The yield of this process is good, generally greater than 80%, however in order to obtain improved qualities in terms of organoleptic properties such as the smell and/or the color of the vanillin, several additional purification steps are necessary, thus reducing the overall yield of this process. The energy efficiency of this process is also globally degraded due to the use of large quantities of solvents.
La demande internationale WO 2014/114590 décrit également un procédé de purification de vanilline naturelle. Ce procédé consiste à évaporer la vanilline naturelle, cette évaporation pouvant être effectuée par distillation ou par évaporation sous vide de vanilline fondue. Ce procédé est susceptible de produire de la vanilline naturelle très pure, avec un bon rendement, avec un dispositif simple à mettre en œuvre et fonctionnant de façon continue pour être compatible avec les procédés industriels. Cependant, un tel procédé pourrait être difficile à mettre en pratique en raison du nombre et de la dimension des équipements nécessaires.
Par ailleurs, la vanilline ou ses dérivés obtenus par un procédé biotechnologique peuvent contenir certaines impuretés ayant des points d'ébullition très proches de la vanilline ou ses dérivés. Ainsi il est nécessaire de dimensionner de manière adaptée les équipements afin de permettre une séparation efficace de la vanilline ou ses dérivés de ces produits. Ceci implique en général un allongement du temps de séjour dans les équipements de distillation ce qui peut générer de nouvelles impuretés du fait de l'instabilité à haute température de la vanilline et/ou impuretés. International application WO 2014/114590 also describes a process for purifying natural vanillin. This process consists in evaporating the natural vanillin, this evaporation being able to be carried out by distillation or by vacuum evaporation of molten vanillin. This process is capable of producing very pure natural vanillin, with a good yield, with a device that is simple to implement and operates continuously to be compatible with industrial processes. However, such a method could be difficult to put into practice due to the number and size of equipment required. Furthermore, vanillin or its derivatives obtained by a biotechnological process may contain certain impurities having boiling points very close to vanillin or its derivatives. It is therefore necessary to size the equipment appropriately in order to allow effective separation of vanillin or its derivatives from these products. This generally implies a lengthening of the residence time in the distillation equipment, which can generate new impurities due to the instability at high temperature of the vanillin and/or impurities.
C'est pourquoi il serait avantageux de disposer d'un procédé amélioré par rapport à ceux proposés dans l'art antérieur, notamment en termes d'impact environnemental et/ou énergétique tout en améliorant le rendement global de la purification ainsi que le rendement en vanilline ou ses dérivés. Il est également important que le procédé de purification de la vanilline permette de produire une vanilline dont les propriétés organoleptiques sont préservées notamment en termes de goût, couleur et/ou odeur. This is why it would be advantageous to have an improved process compared to those proposed in the prior art, in particular in terms of environmental and/or energy impact while improving the overall yield of the purification as well as the yield in vanillin or its derivatives. It is also important that the process for purifying the vanillin makes it possible to produce a vanillin whose organoleptic properties are preserved, in particular in terms of taste, color and/or smell.
Brève description brief description
La présente invention concerne un procédé de purification de vanilline ou ses dérivés obtenus par un procédé biotechnologique comprenant au moins une étape dans laquelle la vanilline ou ses dérivés est séparée de l'alcool vanillique ou ses dérivés. The present invention relates to a process for the purification of vanillin or its derivatives obtained by a biotechnological process comprising at least one step in which the vanillin or its derivatives is separated from the vanillic alcohol or its derivatives.
Description des figures Description of figures
Les figures 1 à 5 schématisent différents procédés de purification de vanilline ou ses dérivés obtenus par un procédé biotechnologique selon la présente invention. Figures 1 to 5 schematize various processes for the purification of vanillin or its derivatives obtained by a biotechnological process according to the present invention.
Description détaillée detailed description
Dans le cadre de la présente invention, et sauf indication contraire, l'expression « compris entre ...et... » inclut les bornes. In the context of the present invention, and unless otherwise indicated, the expression "between ... and ..." includes the terminals.
Dans la présente invention, l'expression « vanilline naturelle » désigne une vanilline obtenue par un procédé biotechnologique. Ainsi un procédé de préparation de vanilline naturelle désigne ici un procédé biotechnologique comprenant la culture d'un microorganisme apte à permettre la transformation d'un substrat de fermentation en vanilline. Le micro-organisme peut être d'origine sauvage ou être un micro organisme génétiquement modifié (GMM) obtenu par biologie moléculaire. Très préférentiellement, il peut s'agir d'un procédé de fermentation d'acide férulique, tel que celui décrit dans la demande de brevet EP 0885968. Selon un aspect particulier, la vanilline peut être produite par un procédé de fermentation de glucose ou d'acide protocatéchuique tel que décrit dans la demande de brevet WO 2013/022881. In the present invention, the expression “natural vanillin” designates a vanillin obtained by a biotechnological process. Thus a process for the preparation of natural vanillin denotes here a biotechnological process comprising the culture of a microorganism capable of allowing the transformation of a fermentation substrate into vanillin. The microorganism may be of wild origin or be a genetically modified microorganism (GMM) obtained by molecular biology. Very preferably, it may be a ferulic acid fermentation process, such as that described in patent application EP 0885968. According to one particular aspect, vanillin may be produced by a glucose or d protocatechuic acid as described in patent application WO 2013/022881.
Dans le cadre de la présente invention, le terme "dérivé de vanilline" se réfère à tout composé pouvant dériver de la vanilline et en particulier à la vanilline sous forme salifiée ou à la glucovanilline. In the context of the present invention, the term “vanillin derivative” refers to any compound which may be derived from vanillin and in particular to vanillin in salified form or to glucovanillin.
Dans le cadre de la présente invention, le terme "dérivé d'alcool vanillique" se réfère à tout composé pouvant dériver de l'alcool vanillique et en particulier à l'alcool vanillique sous forme salifiée ou au glucoside de l'alcool vanillique. In the context of the present invention, the term “derivative of vanillic alcohol” refers to any compound which may derive from vanillic alcohol and in particular to vanillic alcohol in salified form or to the glucoside of vanillic alcohol.
Dans le cadre de la présente invention, le terme "cristallisation" se réfère à un procédé dans lequel une substance passe à l'état solide par un procédé physique, telle que notamment l'abaissement de la températu re.
Dans le cadre de la présente invention, le terme "précipitation" se réfère à un procédé dans lequel une substance passe à l'état solide par une transformation chimique, telle que notamment par protonation grâce à un changement de pH. In the context of the present invention, the term "crystallization" refers to a process in which a substance changes to the solid state by a physical process, such as in particular lowering the temperature. In the context of the present invention, the term “precipitation” refers to a process in which a substance passes into the solid state by a chemical transformation, such as in particular by protonation thanks to a change in pH.
La présente invention concerne un procédé de purification de vanilline ou ses dérivés obtenus par un procédé biotechnologique comprenant au moins une étape dans laquelle la vanilline ou ses dérivés est séparée de l'alcool vanillique ou ses dérivés. The present invention relates to a process for the purification of vanillin or its derivatives obtained by a biotechnological process comprising at least one step in which the vanillin or its derivatives is separated from the vanillic alcohol or its derivatives.
Selon la présente invention, le procédé de purification de la présente invention comprend au moins une étape de cristallisation de la vanilline ou ses dérivés. L'étape de cristallisation permet de purifier de la vanilline ou ses dérivés, obtenus par un procédé biotechnologique, ayant une pureté comprise entre 85% et 99%, de préférence supérieure ou égale à 90%, très préférentiellement supérieure ou égale à 95%. Avantageusement le procédé de cristallisation permet de produire une vanilline ou ses dérivés purifiés ayant une pureté supérieure ou égale à 95%, de préférence supérieure ou égale à 97%, très préférentiellement supérieure ou égale à 99%. La vanilline ayant une pureté comprise entre 85% et 99% comprend en général au moins un autre composé choisi parmi alcool vanillique, acide vanillique, gaïacol, acétovanillone, 4-((4-hydroxy-3-méthoxy-benzyl)oxy)-3-méthoxybenzaldehyde et 4-hydroxy-3-(4- hydroxy-3-méthoxybenzyl)-5-méthoxybenzaldehyde. La teneur en alcool vanillique est en général comprise entre à 0,01% et 15% en poids. According to the present invention, the purification process of the present invention comprises at least one step of crystallization of vanillin or its derivatives. The crystallization step makes it possible to purify vanillin or its derivatives, obtained by a biotechnological process, having a purity of between 85% and 99%, preferably greater than or equal to 90%, very preferably greater than or equal to 95%. Advantageously, the crystallization process makes it possible to produce a vanillin or its purified derivatives having a purity greater than or equal to 95%, preferably greater than or equal to 97%, very preferably greater than or equal to 99%. Vanillin having a purity of between 85% and 99% generally comprises at least one other compound chosen from vanillic alcohol, vanillic acid, guaiacol, acetovanillone, 4-((4-hydroxy-3-methoxy-benzyl)oxy)-3 -methoxybenzaldehyde and 4-hydroxy-3-(4-hydroxy-3-methoxybenzyl)-5-methoxybenzaldehyde. The vanillic alcohol content is generally between 0.01% and 15% by weight.
La cristallisation est généralement conduite dans une solution alcoolique. De préférence le solvant utilisé pour la cristallisation peut être un alcool soluble avec l'eau, de préférence l'éthanol. Le solvant utilisé pour la cristallisation peut être un mélange eau/alcool. En général, la quantité d'alcool est comprise entre 2% et 40% en masse, de préférence comprise entre 5% et 35% en masse, et très préférentiellement comprise entre 15% à 25% en masse. De manière générale, lors de la cristallisation, la concentration en vanilline, en début de cristallisation, est comprise entre 5% et 60% en poids, de préférence comprise entre 10% et 50% en poids, avantageusement comprise entre 15% et 35% en poids, et encore plus préférentiellement entre 15% et 25%. Très avantageusement la cristallisation permet la séparation de la vanilline ou ses dérivés et l'alcool vanillique ou ses dérivés, cette séparation est avantageusement conduite sans dégradation de la vanilline ou ses dérivés. De préférence la cristallisation permet la séparation de la vanilline et l'alcool vanillique, cette séparation est avantageusement conduite sans dégradation de la vanilline La cristallisation est réalisée à une température comprise entre 0°C et 50°C. Le rendement de la cristallisation est généralement supérieur ou égal à 80%. La vanilline obtenue à l'issue de l'étape de cristallisation présente généralement une couleur en solution éthanolique à 10% en poids inférieure ou égale à 150 Hazen, de préférence inférieure ou égale à 100 Hazen, et très préférentiellement inférieure ou égale à 50 Hazen. Crystallization is usually carried out in an alcoholic solution. Preferably the solvent used for the crystallization can be a water-soluble alcohol, preferably ethanol. The solvent used for the crystallization can be a water/alcohol mixture. In general, the amount of alcohol is between 2% and 40% by weight, preferably between 5% and 35% by weight, and very preferably between 15% and 25% by weight. Generally, during crystallization, the vanillin concentration, at the start of crystallization, is between 5% and 60% by weight, preferably between 10% and 50% by weight, advantageously between 15% and 35% by weight, and even more preferably between 15% and 25%. Very advantageously the crystallization allows the separation of the vanillin or its derivatives and the vanillic alcohol or its derivatives, this separation is advantageously carried out without degradation of the vanillin or its derivatives. Preferably the crystallization allows the separation of the vanillin and the vanillic alcohol, this separation is advantageously carried out without degradation of the vanillin. The crystallization is carried out at a temperature comprised between 0°C and 50°C. The crystallization yield is generally greater than or equal to 80%. The vanillin obtained at the end of the crystallization step generally has a color in 10% by weight ethanolic solution less than or equal to 150 Hazen, preferably less than or equal to 100 Hazen, and very preferably less than or equal to 50 Hazen .
La présente invention concerne un procédé de purification de vanilline ou ses dérivés obtenus par un procédé biotechnologique dans laquelle la vanilline ou ses dérivés est séparée de l'alcool vanillique ou ses dérivés. Avantageusement le procédé de purification de vanilline ou ses dérivés est particulièrement optimisé et permet de réduire la quantité de solvant organique utilisé. En général, la quantité de solvant organique utilisée dans le procédé de purification est réduite d'au moins 5% par rapport aux procédés de purification de vanilline obtenue par un procédé biotechnologique. La réduction de solvant est calculée par rapport à des procédés utilisant au moins un solvant organique. La quantité de solvant utilisée est calculée à partir de toute quantité de solvant utilisée pour la purification entre le moût de fermentation jusqu'à l'obtention de la vanilline purifiée, cristallisée. Le procédé est ainsi amélioré par
rapport aux procédés de l'état de la technique en ce qu'il a un impact écologique et/ou environnemental réduit. The present invention relates to a process for the purification of vanillin or its derivatives obtained by a biotechnological process in which the vanillin or its derivatives is separated from the vanillic alcohol or its derivatives. Advantageously, the process for purifying vanillin or its derivatives is particularly optimized and makes it possible to reduce the quantity of organic solvent used. In general, the amount of organic solvent used in the purification process is reduced by at least 5% compared to purification processes for vanillin obtained by a biotechnological process. Solvent reduction is calculated relative to processes using at least one organic solvent. The amount of solvent used is calculated from any amount of solvent used for purification between the fermentation broth until the purified, crystallized vanillin is obtained. The process is thus improved by compared to the processes of the state of the art in that it has a reduced ecological and/or environmental impact.
La présente invention concerne un procédé de purification de vanilline ou ses dérivés obtenus par un procédé biotechnologique dans laquelle la vanilline ou ses dérivés est séparée de l'alcool vanillique ou ses dérivés. Avantageusement le procédé de la présente invention permet de valoriser l'alcool vanillique ou ses dérivés. L'alcool vanillique ou ses dérivés peuvent en effet être récupérés dans le filtrat issu de la cristallisation. Contrairement aux procédés de l'art antérieur, cet alcool vanillique ou ses dérivés peuvent ensuite être valorisés en tant qu'intermédiaire de synthèse notamment pour la préparation de composés organiques pour l'industrie cosmétique ou la parfumerie. Le procédé de la présente invention ne dégrade pas l'alcool vanillique ou ses dérivés. The present invention relates to a process for the purification of vanillin or its derivatives obtained by a biotechnological process in which the vanillin or its derivatives is separated from the vanillic alcohol or its derivatives. Advantageously, the process of the present invention makes it possible to upgrade vanillic alcohol or its derivatives. The vanillic alcohol or its derivatives can indeed be recovered in the filtrate resulting from the crystallization. Unlike the processes of the prior art, this vanillic alcohol or its derivatives can then be upgraded as a synthesis intermediate, in particular for the preparation of organic compounds for the cosmetics or perfumery industry. The process of the present invention does not degrade vanillic alcohol or its derivatives.
Dans le cadre de la présente invention, à l'issue d'un procédé biotechnologique de préparation de vanilline ou ses dérivés, la vanilline, ou ses dérivés, est en solution aqueuse dans un moût de fermentation. Ainsi le procédé de la présente invention consiste à purifier une solution aqueuse de vanilline ou ses dérivés. De manière générale, la concentration en vanilline dans la solution aqueuse est comprise entre 0,2 et 5% en poids, de préférence comprise entre 0,8 et 2,5% en poids, très préférentiellement entre 1,0 et 1,8% en poids. La solution aqueuse comprend en outre : de la biomasse, en général, la quantité de biomasse est comprise entre 0,5 et 5% en poids de matière sèche, de préférence comprise entre 1,0 et 2,0% en poids de matière sèche ; de l'alcool vanillique, en général, la quantité d'alcool vanillique est comprise entre 0,01% et 0,5% en poids, de préférence comprise entre 0,05% et 0,3% en poids; de l'acide vanillique, en général, la quantité d'acide vanillique est comprise entre 0,01% et 0,5% en poids, de préférence comprise entre 0,05% et 0,3% en poids. In the context of the present invention, at the end of a biotechnological process for the preparation of vanillin or its derivatives, the vanillin or its derivatives is in aqueous solution in a fermentation broth. Thus the process of the present invention consists in purifying an aqueous solution of vanillin or its derivatives. Generally, the vanillin concentration in the aqueous solution is between 0.2 and 5% by weight, preferably between 0.8 and 2.5% by weight, very preferably between 1.0 and 1.8% in weight. The aqueous solution further comprises: biomass, in general, the amount of biomass is between 0.5 and 5% by weight of dry matter, preferably between 1.0 and 2.0% by weight of dry matter ; vanillic alcohol, in general, the amount of vanillic alcohol is between 0.01% and 0.5% by weight, preferably between 0.05% and 0.3% by weight; vanillic acid, in general, the amount of vanillic acid is between 0.01% and 0.5% by weight, preferably between 0.05% and 0.3% by weight.
La solution aqueuse peut également comprendre d'autres composés tels que acide férulique, et dérivés d'acide férulique, acide coumarique, para-hydroxybenzaldéhyde, gaïacol. Ces composés peuvent être séparés de la vanilline ou ses dérivés selon le procédé de la présente invention. Avantageusement au moins un composé choisi parmi l'acide férulique, les dérivés d'acide férulique, l'acide coumarique, le para-hydroxybenzaldéhyde ou le gaïacol peut être valorisé notamment en tant qu'intermédiaire de synthèse. The aqueous solution can also comprise other compounds such as ferulic acid, and derivatives of ferulic acid, coumaric acid, para-hydroxybenzaldehyde, guaiacol. These compounds can be separated from vanillin or its derivatives according to the process of the present invention. Advantageously, at least one compound chosen from ferulic acid, ferulic acid derivatives, coumaric acid, para-hydroxybenzaldehyde or guaiacol can be utilized in particular as a synthesis intermediate.
Le procédé de purification de la présente invention peut comprendre au moins une étape consistant en une séparation de la biomasse de la solution aqueuse de vanilline ou ses dérivés. Cette étape est une étape de séparation d'une phase solide : la biomasse, d'une phase liquide. La phase liquide obtenue à l'issue de l'étape de séparation de la biomasse est une phase aqueuse comprenant la vanilline ou ses dérivés. The purification process of the present invention may comprise at least one step consisting of a separation of the biomass from the aqueous solution of vanillin or its derivatives. This stage is a stage of separation of a solid phase: the biomass, from a liquid phase. The liquid phase obtained at the end of the biomass separation step is an aqueous phase comprising vanillin or its derivatives.
Selon un aspect, l'étape de séparation de la biomasse peut être effectuée par filtration telle que filtration frontale ou filtration tangentielle, en particulier filtration sur membrane, telle que microfiltration, ultrafiltration, nanofiltration, ou osmose inverse. La filtration sur membrane peut être opérée en concentration ou en diafiltration. Avantageusement lorsque l'étape de séparation de la biomasse est une filtration frontale, il est possible d'ajouter des adjuvants afin d'améliorer l'efficacité de la filtration.
Afin d'améliorer l'efficacité de la séparation solide/liquide il est possible de réaliser plusieurs étapes de séparation solide/liquide, notamment pour retirer les particules solides les plus petites. According to one aspect, the step of separating the biomass can be carried out by filtration such as frontal filtration or tangential filtration, in particular membrane filtration, such as microfiltration, ultrafiltration, nanofiltration, or reverse osmosis. Membrane filtration can be carried out in concentration or in diafiltration. Advantageously when the biomass separation step is a frontal filtration, it is possible to add adjuvants in order to improve the efficiency of the filtration. In order to improve the efficiency of the solid/liquid separation, it is possible to carry out several solid/liquid separation steps, in particular to remove the smallest solid particles.
Selon un aspect particulier, l'étape de séparation de la biomasse peut être réalisée par une ou plusieurs membranes de microfiltration, en particulier ayant une limite de coupe d'environ 0,2 pm, suivie d'une ou plusieurs ultrafiltrations ayant une limite de coupe plus petite que celle de la microfiltration. Dans cette configuration, la vanilline est solubilisée en phase aqueuse et la biomasse est retenue par les membranes. Avantageusement l'ultrafiltration permet également de la séparation de molécules solubilisées dans le moût de fermentation. According to a particular aspect, the biomass separation step can be carried out by one or more microfiltration membranes, in particular having a cutting limit of approximately 0.2 μm, followed by one or more ultrafiltrations having a limit of smaller cut than microfiltration. In this configuration, the vanillin is dissolved in the aqueous phase and the biomass is retained by the membranes. Advantageously, ultrafiltration also allows the separation of molecules dissolved in the fermentation broth.
Afin d'améliorer le rendement en vanilline ou ses dérivés dans la phase aqueuse, un solvant, de préférence de l'eau, est ajouté au cours de l'étape de filtration. De manière générale, la quantité de solvant ajoutée est comprise entre 0,5 et 5 équivalents en volume de moût de fermentation. In order to improve the yield of vanillin or its derivatives in the aqueous phase, a solvent, preferably water, is added during the filtration step. In general, the amount of solvent added is between 0.5 and 5 equivalents by volume of fermentation broth.
Selon un aspect la microfiltration, l'ultrafiltration ou la diafiltration peuvent être couplées à une étape de nanofiltration ou d'osmose inverse. En effet la nanofiltration permet d'augmenter la concentration en vanilline dans le rétentat de l'étape de nanofiltration tandis que l'eau passe au travers de la membrane (perméat de l'étape de nanofiltration). Le perméat de cette étape de nanofiltration peut avantageusement être recyclé. De manière générale, l'osmose inverse a une limite de coupe inférieure ou égale 100 Da. De manière générale, la nanofiltration a une limite de coupe inférieure ou égale à 400 Da. De manière générale, la nanofiltration a une limite de coupe supérieure ou égale à 100 Da, par exemple limite de coupe comprise entre 100 et 250 Da. According to one aspect, the microfiltration, ultrafiltration or diafiltration can be coupled with a nanofiltration or reverse osmosis step. In fact, nanofiltration makes it possible to increase the vanillin concentration in the retentate from the nanofiltration step while the water passes through the membrane (permeate from the nanofiltration step). The permeate from this nanofiltration step can advantageously be recycled. Generally speaking, reverse osmosis has a cut limit of less than or equal to 100 Da. In general, nanofiltration has a cut limit of less than or equal to 400 Da. In general, nanofiltration has a cutting limit greater than or equal to 100 Da, for example cutting limit between 100 and 250 Da.
Préalablement à cette étape de séparation de la biomasse de la solution aqueuse de vanilline ou ses dérivés, le moût de fermentation peut être stabilisé. Prior to this step of separating the biomass from the aqueous solution of vanillin or its derivatives, the fermentation must can be stabilized.
Dans le cadre de la présente invention, le terme « stabilisation » se réfère à toute méthode permettant d'éviter la dégradation, notamment par réduction, de la vanilline ou ses dérivés entre la fin de la fermentation et le procédé de purification. In the context of the present invention, the term “stabilization” refers to any method making it possible to avoid the degradation, in particular by reduction, of the vanillin or its derivatives between the end of the fermentation and the purification process.
Selon un premier aspect, la stabilisation peut être effectuée par l'ajout d'au moins un composé. Le composé est préférentiellement choisi parmi le benzoate de sodium, l'acide ascorbique et ses sels, le sorbate de potassium, de calcium ou de sodium, le sulfate de zinc, l'acide propanoïque, acide acétique ou ses sels, diacétate de sodium. De préférence la quantité de composé ajoutée est comprise entre 0,2 g/L et 6 g/L. According to a first aspect, the stabilization can be carried out by adding at least one compound. The compound is preferably chosen from sodium benzoate, ascorbic acid and its salts, potassium, calcium or sodium sorbate, zinc sulphate, propanoic acid, acetic acid or its salts, sodium diacetate. Preferably, the amount of compound added is between 0.2 g/L and 6 g/L.
Selon un autre aspect, la stabilisation peut être effectuée par changement de la température du moût de fermentation. En général, la température est contrôlée de manière à atteindre une température comprise entre 15°C et 23°C, de préférence comprise entre 18°C et 21°C. According to another aspect, the stabilization can be carried out by changing the temperature of the fermentation broth. In general, the temperature is controlled so as to reach a temperature between 15°C and 23°C, preferably between 18°C and 21°C.
Selon un autre aspect, la stabilisation peut être effectuée par changement du pH du moût de fermentation. En général, le pH est contrôlé de manière à atteindre un pH inférieur ou égal à 7,5, de préférence inférieur ou égal à 7, très préférentiellement inférieur ou égal à 6.8. En général, le pH est contrôlé de manière à atteindre un pH supérieur ou égal à 5,0, de préférence supérieur ou égal à 6.According to another aspect, the stabilization can be carried out by changing the pH of the fermentation broth. In general, the pH is controlled so as to reach a pH less than or equal to 7.5, preferably less than or equal to 7, very preferably less than or equal to 6.8. In general, the pH is controlled so as to achieve a pH greater than or equal to 5.0, preferably greater than or equal to 6.
Selon un autre aspect, le moût de fermentation peut également être pasteurisé. En général, le moût de fermentation est alors chauffé à une température comprise entre 50°C et 90°C, de préférence comprise
entre 60°C et 80°C. Le chauffage est en général maintenu pendant une durée comprise entre 10 min et 120 min, de préférence comprise entre 15 min et 45 min, par exemple pendant 20 min. According to another aspect, the fermentation broth can also be pasteurized. In general, the fermentation must is then heated to a temperature between 50°C and 90°C, preferably between between 60°C and 80°C. The heating is generally maintained for a period comprised between 10 min and 120 min, preferably comprised between 15 min and 45 min, for example for 20 min.
Selon un autre aspect, le moût de fermentation peut être stabilisé par ultrasons. En général des ultrasons sont émis dans le moût de fermentation pendant une durée comprise entre 10 min et 120 min. According to another aspect, the fermentation must can be stabilized by ultrasound. In general, ultrasound is emitted in the fermentation must for a period of between 10 min and 120 min.
Selon un aspect particulier ces aspects peuvent être réalisés séparément ou conjointement, ainsi, à titre d'exemple non limitatif, il est possible de modifier la température, le pH et d'ajouter un composé selon les conditions décrites ci-dessus. According to a particular aspect, these aspects can be carried out separately or jointly, thus, by way of nonlimiting example, it is possible to modify the temperature, the pH and to add a compound according to the conditions described above.
Parmi ces méthodes, les méthodes sans ajout de composés sont avantageuses, sans vouloir être lié par une quelconque théorie, elles permettent d'éviter de possibles effets délétères sur la vanilline ou ses dérivés notamment en termes d'odeur ou de couleur. Among these methods, the methods without adding compounds are advantageous, without wishing to be bound by any theory whatsoever, they make it possible to avoid possible deleterious effects on vanillin or its derivatives, in particular in terms of odor or color.
Cependant l'ajout de certains composés choisis pour leur compatibilité avec la vanilline ou ses dérivés et l'absence d'effet secondaire sur la vanilline ou ses dérivés peut se révéler particulièrement avantageuse pour faciliter la suite du procédé de purification de la vanilline ou ses dérivés. However, the addition of certain compounds chosen for their compatibility with vanillin or its derivatives and the absence of side effects on vanillin or its derivatives can prove to be particularly advantageous for facilitating the rest of the process for purifying vanillin or its derivatives. .
Le procédé de purification comprend généralement au moins une étape d'extraction liquide/liquide permettant de récupérer la vanilline ou ses dérivés dans une solution organique. L'étape d'extraction liquide/liquide permet avantageusement de transférer la vanilline ou ses dérivés en solution aqueuse dans le moût de fermentation ou à l'issue d'une séparation solide/liquide du moût de fermentation dans une phase organique. Ainsi à l'issue de l'étape d'extraction liquide/liquide, on obtient une phase organique comprenant la vanilline ou ses dérivés. L'étape d'extraction liquide/liquide permet avantageusement la séparation de la vanilline ou ses dérivés de composés très solubles dans l'eau tels que l'acide vanillique ou ses dérivés, l'acide férulique. The purification process generally comprises at least one liquid/liquid extraction step making it possible to recover the vanillin or its derivatives in an organic solution. The liquid/liquid extraction step advantageously makes it possible to transfer the vanillin or its derivatives in aqueous solution into the fermentation must or, after a solid/liquid separation of the fermentation must, into an organic phase. Thus, at the end of the liquid/liquid extraction step, an organic phase is obtained comprising vanillin or its derivatives. The liquid/liquid extraction step advantageously allows the separation of vanillin or its derivatives from compounds that are very soluble in water such as vanillic acid or its derivatives, ferulic acid.
De manière générale, le pH de la solution aqueuse est compris entre 5 et 8, de préférence compris entre 5,5 et 7,5, très préférentiellement compris entre 6 et 7. Generally, the pH of the aqueous solution is between 5 and 8, preferably between 5.5 and 7.5, very preferably between 6 and 7.
De manière générale, le solvant d'extraction est choisi pour ces propriétés de solubilisation de la vanilline ou ses dérivés, avantageusement le solvant peut être d'origine biosourcée. Selon un aspect, le solvant choisi est compatible avec les normes de l'industrie alimentaire, notamment FEMA GRAS, non- miscible à l'eau. De préférence le solvant est choisi parmi méthyléthylcétone, méthylisobutylcétone, acétate d'éthyle, acétate d'isopropyle ou leurs mélanges. In general, the extraction solvent is chosen for these solubilization properties of vanillin or its derivatives, advantageously the solvent can be of biosourced origin. According to one aspect, the solvent chosen is compatible with the standards of the food industry, in particular FEMA GRAS, immiscible with water. Preferably, the solvent is chosen from methyl ethyl ketone, methyl isobutyl ketone, ethyl acetate, isopropyl acetate or mixtures thereof.
L'étape d'extraction liquide/liquide peut être une extraction liquide-liquide discontinue. Afin de maximiser la quantité de vanilline ou ses dérivés obtenus dans la phase organique, le ratio volumique de solvant par rapport à la solution aqueuse de vanilline ou ses dérivés est compris entre 1 :5 et 5 :1, de préférence compris entre 1 : 1 et 5 :1, de préférence compris entre 1,5 :1 et 3 :1. The liquid/liquid extraction step can be a discontinuous liquid-liquid extraction. In order to maximize the amount of vanillin or its derivatives obtained in the organic phase, the volume ratio of solvent relative to the aqueous solution of vanillin or its derivatives is between 1:5 and 5:1, preferably between 1:1 and 5:1, preferably between 1.5:1 and 3:1.
Selon un autre aspect, l'étape d'extraction liquide/liquide peut être réalisée en continu. De manière générale, le ratio volumique de solvant par rapport à la solution aqueuse de vanilline ou ses dérivés est compris entre 5 : 1 et 1 :2, de préférence compris entre 3:1 et 1:1. According to another aspect, the liquid/liquid extraction step can be carried out continuously. In general, the volume ratio of solvent relative to the aqueous solution of vanillin or its derivatives is between 5:1 and 1:2, preferably between 3:1 and 1:1.
Le rendement en vanilline ou ses dérivés de l'étape d'extraction liquide/liquide est généralement supérieur ou égal à 95%, de préférence supérieur ou égal à 97%, très préférentiellement supérieur ou égal à 98%.
Selon un aspect particulier, les étapes de séparation de la biomasse et d'extraction liquide/liquide peuvent être réalisées simultanément. Cet aspect particulier permet d'extraire la vanilline ou ses dérivés dans le solvant organique à partir du moût de fermentation. La biomasse est ensuite séparée du système bi-phasique. Ce procédé est avantageux en ce que la perte en vanilline ou ses dérivés dans la biomasse est réduite. Cette étape de séparation peut notamment être effectuée en continu par centrifugation en particulier en employant une centrifugeuse deux ou trois phases ou un extracteur à contre-courant. The yield of vanillin or its derivatives from the liquid/liquid extraction stage is generally greater than or equal to 95%, preferably greater than or equal to 97%, very preferably greater than or equal to 98%. According to a particular aspect, the stages of separation of the biomass and of liquid/liquid extraction can be carried out simultaneously. This particular aspect makes it possible to extract the vanillin or its derivatives in the organic solvent from the fermentation broth. The biomass is then separated from the two-phase system. This process is advantageous in that the loss of vanillin or its derivatives in the biomass is reduced. This separation step can in particular be carried out continuously by centrifugation, in particular by using a two- or three-phase centrifuge or a counter-current extractor.
La concentration (C) de la solution organique de vanilline ou ses dérivés obtenue à l'issue de l'étape d'extraction liquide/liquide est généralement comprise entre 0,1% en poids et 10% en poids. The concentration (C) of the organic solution of vanillin or its derivatives obtained at the end of the liquid/liquid extraction step is generally between 0.1% by weight and 10% by weight.
Optionnellement une étape de stripping peut être conduite sur le flux aqueux obtenu à l'issue de l'étape d'extraction liquide-liquide. Avantageusement l'étape de stripping permet la récupération de composés organiques contenus dans le flux aqueux, notamment de la vanilline ou ses dérivés. Ainsi le stripping permet d'améliorer le rendement de vanilline ou ses dérivés. L'étape de stripping permet également de faciliter le traitement des effluents aqueux. Optionally, a stripping step can be carried out on the aqueous stream obtained at the end of the liquid-liquid extraction step. Advantageously, the stripping step allows the recovery of organic compounds contained in the aqueous flow, in particular vanillin or its derivatives. Thus stripping makes it possible to improve the yield of vanillin or its derivatives. The stripping step also makes it possible to facilitate the treatment of the aqueous effluents.
Le procédé de la présente invention comprend au moins une étape de concentration d'une solution aqueuse ou organique de vanilline ou ses dérivés. The method of the present invention comprises at least one step of concentration of an aqueous or organic solution of vanillin or its derivatives.
Selon un aspect particulier, la concentration peut être réalisée sur une solution aqueuse de vanilline ou ses dérivés obtenue à l'issue de l'étape de séparation de la biomasse. Selon un autre aspect, la concentration peut être réalisée sur une solution organique de vanilline ou ses dérivés obtenue à l'issue de l'extraction liquide/liquide. En général à l'issue de l'étape de concentration, la vanilline ou ses dérivés se présente sous la forme liquide ou solide en fonction de la température. En général, au moins 95% du solvant a été séparé de la vanilline ou ses dérivés. Cependant l'étape de concentration peut consister en une ou plusieurs étapes de concentration. According to a particular aspect, the concentration can be carried out on an aqueous solution of vanillin or its derivatives obtained at the end of the stage of separation of the biomass. According to another aspect, the concentration can be carried out on an organic solution of vanillin or its derivatives obtained after the liquid/liquid extraction. In general, at the end of the concentration step, the vanillin or its derivatives is in liquid or solid form depending on the temperature. In general, at least 95% of the solvent has been separated from the vanillin or its derivatives. However, the concentration step can consist of one or more concentration steps.
Ainsi selon un aspect particulier, au moins 95% de la quantité de solvant présent dans la solution organique de vanilline ou ses dérivés obtenue à l'issue de l'extraction liquide-liquide peut être évaporée.Thus, according to a particular aspect, at least 95% of the quantity of solvent present in the organic solution of vanillin or its derivatives obtained at the end of the liquid-liquid extraction can be evaporated.
Selon un autre aspect, la concentration de la solution organique obtenue à l'issue de l'étape d'extraction liquide/liquide peut être partielle, pour aboutir à la formation d'une solution de vanilline ou de ses dérivés concentrée (Cl), de préférence ayant une concentration plus élevée que la concentration (C) de la solution organique de vanilline ou ses dérivés obtenue à l'issue de l'étape d'extraction liquide/liquide.According to another aspect, the concentration of the organic solution obtained at the end of the liquid/liquid extraction step can be partial, to result in the formation of a solution of vanillin or its concentrated derivatives (Cl), preferably having a higher concentration than the concentration (C) of the organic solution of vanillin or its derivatives obtained at the end of the liquid/liquid extraction step.
Selon un aspect particulier, la solution organique de vanilline ou ses dérivés obtenue à l'issue de l'étape d'extraction liquide/liquide est concentrée de manière à obtenir une solution organique de vanilline ou ses dérivés (Cl) ayant une concentration comprise entre 10% en poids et 95% en poids. According to a particular aspect, the organic solution of vanillin or its derivatives obtained at the end of the liquid/liquid extraction step is concentrated so as to obtain an organic solution of vanillin or its derivatives (Cl) having a concentration of between 10% by weight and 95% by weight.
La solution organique de vanilline ou ses dérivés (Cl) peut être soumise à une ou plusieurs étapes de concentration subséquentes de manière à obtenir de la vanilline ou ses dérivés sous forme liquide ou solide en fonction de la température. The organic solution of vanillin or its derivatives (Cl) can be subjected to one or more subsequent concentration steps so as to obtain vanillin or its derivatives in liquid or solid form depending on the temperature.
L'étape de concentration peut être réalisée en procédé continu ou en procédé batch. The concentration step can be carried out in a continuous process or in a batch process.
En procédé batch, l'étape de concentration peut être réalisée dans un réacteur agité ou dans une colonne de distillation. Préférentiellement l'étape de concentration est réalisée sous vide, de préférence
à une pression comprise entre 5 mbar et 300 mbar, de préférence entre 50 mbar et 250 mbar. L'étape de concentration est généralement réalisée à une température comprise entre 25°C et 100°C. In a batch process, the concentration step can be carried out in a stirred reactor or in a distillation column. Preferably, the concentration step is carried out under vacuum, preferably at a pressure between 5 mbar and 300 mbar, preferably between 50 mbar and 250 mbar. The concentration step is generally carried out at a temperature between 25°C and 100°C.
En procédé continu, l'étape de concentration peut être réalisée à l'aide de colonnes de distillation à plateaux ou garnies, d'évaporateurs à film tombant, d'évaporateurs à film raclé ou de colonnes à cloison. In a continuous process, the concentration step can be carried out using tray or packed distillation columns, falling film evaporators, wiped film evaporators or partition columns.
De manière générale, l'étape de concentration est réalisée à une pression en tête de distillation comprise entre 0,5 bar et 5 bar, de préférence comprise entre 1 bar et 3 bar. La température, en tête de distillation, est en général comprise entre 75°C et 150°C, de préférence comprise entre 85°C et 120°C et de manière très préférée comprise entre 90°C et 110°C. In general, the concentration step is carried out at a pressure at the distillation head of between 0.5 bar and 5 bar, preferably between 1 bar and 3 bar. The temperature at the distillation head is generally between 75°C and 150°C, preferably between 85°C and 120°C and very preferably between 90°C and 110°C.
Avantageusement l'étape de concentration est réalisée de manière à réduire le temps de passage de la vanilline ou ses dérivés dans les réacteurs ou colonnes. Advantageously, the concentration step is carried out so as to reduce the transit time of the vanillin or its derivatives in the reactors or columns.
L'étape de concentration permet de récupérer la vanilline ou ses dérivés en pied de colonne tandis que le solvant est récupéré en tête de colonne. La vanilline ou ses dérivés en pied de colonne présente en général une pureté supérieure ou égale à 90%. D'autres composés sont présents avec la vanilline ou ses dérivés en pied de colonne notamment l'alcool vanillique ou ses dérivés. The concentration step makes it possible to recover the vanillin or its derivatives at the bottom of the column while the solvent is recovered at the top of the column. The vanillin or its derivatives at the bottom of the column generally have a purity greater than or equal to 90%. Other compounds are present with vanillin or its derivatives at the bottom of the column, in particular vanillic alcohol or its derivatives.
Le procédé de purification de la présente invention peut comprendre au moins une étape dans laquelle la vanilline ou ses dérivés est séparée de composés ayant un point d'ébullition plus élevé que celui de la vanilline ou ses dérivés. Cette étape peut être une étape de dégoudronnage. The purification process of the present invention may comprise at least one step in which vanillin or its derivatives is separated from compounds having a higher boiling point than that of vanillin or its derivatives. This step can be a tar removal step.
L'étape de dégoudronnage peut être conduite dans une colonne de distillation, une colonne à cloison, un évaporateur à film tombant, ou un évaporateur à film raclé. The tar removal step can be carried out in a distillation column, a partition column, a falling film evaporator, or a wiped film evaporator.
Le procédé de purification de la présente invention comprend au moins une étape de cristallisation de la vanilline ou ses dérivés telle que décrite précédemment. La cristallisation peut notamment être réalisée sur de la vanilline ou ses dérivés obtenus à l'issue d'au moins une étape choisie parmi extraction liquide/liquide, concentration et dégoudronnage. The purification process of the present invention comprises at least one step of crystallization of vanillin or its derivatives as described above. The crystallization can in particular be carried out on vanillin or its derivatives obtained after at least one step chosen from liquid/liquid extraction, concentration and tar removal.
Le procédé de purification de la présente invention peut en outre comprendre une étape de précipitation de la vanilline ou ses dérivés en présence de la biomasse. Cette étape de précipitation est en général préliminaire à l'étape de séparation de la biomasse. La précipitation de la vanilline ou ses dérivés en présence de la biomasse est en général réalisée à une température comprise entre 0°C et 6°C. Cette étape peut être simultanée à une étape de stabilisation du moût de fermentation, notamment par modification du pH. Cet aspect permet ensuite la séparation de la biomasse de la phase liquide. La vanilline ou ses dérivés étant sous forme solide est récupérée dans le gâteau avec la biomasse. Le gâteau est avantageusement repris avec un solvant dans lequel la vanilline ou ses dérivés est soluble, pour permettre la formation d'une phase solide et d'une phase organique de vanilline ou ses dérivés liquide qui peut être purifiée selon les différentes étapes de concentration, de dégoudronnage et/ou de cristallisation telles que décrites précédemment. The purification process of the present invention may further comprise a step of precipitation of vanillin or its derivatives in the presence of the biomass. This precipitation step is generally preliminary to the biomass separation step. The precipitation of vanillin or its derivatives in the presence of biomass is generally carried out at a temperature between 0°C and 6°C. This step can be simultaneous with a step for stabilizing the fermentation broth, in particular by modifying the pH. This aspect then allows the separation of the biomass from the liquid phase. The vanillin or its derivatives being in solid form is recovered in the cake with the biomass. The cake is advantageously taken up with a solvent in which the vanillin or its derivatives is soluble, to allow the formation of a solid phase and an organic phase of vanillin or its liquid derivatives which can be purified according to the different concentration stages, tar removal and/or crystallization as described above.
Selon un autre aspect de la présente invention, le procédé de purification de vanilline ou ses dérivés obtenue par un procédé biotechnologique est caractérisé en ce qu'aucun solvant organique n'est utilisé à l'exception du solvant utilisé lors de la cristallisation. Ainsi selon un aspect particulier de la présente
invention, la quantité de solvant organique utilisé est réduite de 100% par rapport aux procédés de l'état de la technique. According to another aspect of the present invention, the process for purifying vanillin or its derivatives obtained by a biotechnological process is characterized in that no organic solvent is used except for the solvent used during the crystallization. Thus, according to a particular aspect of the present invention, the quantity of organic solvent used is reduced by 100% compared to the methods of the state of the art.
Selon un aspect particulier, le procédé de purification de vanilline ou ses dérivés obtenus par un procédé biotechnologique et, préalablement à l'étape de cristallisation, peut comprendre au moins une étape de séparation solide/liquide, de concentration et/ou de dégoudronnage telles que décrites précédemment sans utilisation de solvant organique. According to one particular aspect, the method for purifying vanillin or its derivatives obtained by a biotechnological method and, prior to the crystallization step, may comprise at least one step of solid/liquid separation, concentration and/or tar removal such as previously described without the use of organic solvent.
Selon un premier mode de réalisation représenté par la figure 1, le moût de fermentation est soumis à une étape de stabilisation. Ce moût de fermentation stabilisé est alors centrifugé avec une centrifugeuse à assiette permettant la séparation de la biomasse. Un solvant organique est ajouté simultanément pour permettre d'extraire la vanilline en solution organique, les phases aqueuses et organiques sont séparées. La phase organique est alors soumise à une concentration, de préférence en utilisant un évaporateur à film raclé, et/ou un évaporateur à film tombant. Le solvant organique évaporé est recyclé dans l'étape de séparation de la biomasse. La vanilline est alors soumise à une deuxième étape d'évaporation, de préférence dans un évaporateur à film raclé de manière à séparer la vanilline des lourds. La vanilline est récupérée en tête d'évaporateur avec d'éventuelles impuretés telles que l'alcool vanillique. Enfin ce flux récupéré en tête d'évaporateur est cristallisé pour permettre la préparation d'une vanilline cristallisée ayant une pureté supérieure ou égale à 99,5% et ayant une couleur en solution éthanolique à 10% en poids inférieure ou égale à 150 Hazen, de préférence inférieure ou égale à 100 Hazen, et très préférentiellement inférieur ou égale à 50 Hazen. According to a first embodiment represented by FIG. 1, the fermentation broth is subjected to a stabilization step. This stabilized fermentation broth is then centrifuged with a plate centrifuge allowing the separation of the biomass. An organic solvent is added simultaneously to make it possible to extract the vanillin in organic solution, the aqueous and organic phases are separated. The organic phase is then subjected to concentration, preferably using a wiped film evaporator, and/or a falling film evaporator. The evaporated organic solvent is recycled to the biomass separation step. The vanillin is then subjected to a second stage of evaporation, preferably in a wiped film evaporator so as to separate the vanillin from the heavies. The vanillin is recovered at the head of the evaporator with any impurities such as vanillic alcohol. Finally, this stream recovered at the head of the evaporator is crystallized to allow the preparation of a crystallized vanillin having a purity greater than or equal to 99.5% and having a color in ethanolic solution at 10% by weight less than or equal to 150 Hazen, preferably less than or equal to 100 Hazen, and very preferably less than or equal to 50 Hazen.
Selon un deuxième mode de réalisation, également représenté par la figure 1, le moût de fermentation est soumis à une étape de stabilisation. Ce moût de fermentation stabilisé est alors décanté, puis filtré permettant la séparation de la biomasse. Un solvant organique est ajouté simultanément pour permettre d'extraire la vanilline en solution organique, les phases aqueuses et organiques sont séparées. La phase organique est alors soumise à une concentration par distillation sous vide. Le solvant organique évaporé peut être recyclé dans l'étape de séparation de la biomasse. La vanilline est alors soumise à une deuxième étape d'évaporation, de préférence dans un évaporateur à film raclé de manière à séparer la vanilline et les lourds. La vanilline est récupérée en tête de l'évaporateur avec d'éventuelles impuretés telles que l'alcool vanillique. Enfin ce flux récupéré en tête d'évaporateur est cristallisé pour permettre la préparation d'une vanilline cristallisée ayant une pureté supérieure ou égale à 99,9% et ayant une couleur en solution éthanolique à 10% en poids inférieure ou égale à 150 Hazen, de préférence inférieure ou égale à 100 Hazen, et très préférentiellement inférieur ou égale à 50 Hazen.According to a second embodiment, also represented by FIG. 1, the fermentation broth is subjected to a stabilization step. This stabilized fermentation must is then decanted, then filtered allowing the separation of the biomass. An organic solvent is added simultaneously to make it possible to extract the vanillin in organic solution, the aqueous and organic phases are separated. The organic phase is then subjected to concentration by vacuum distillation. The evaporated organic solvent can be recycled to the biomass separation step. The vanillin is then subjected to a second stage of evaporation, preferably in a wiped film evaporator so as to separate the vanillin and the heavies. The vanillin is recovered at the top of the evaporator with any impurities such as vanillic alcohol. Finally, this stream recovered at the head of the evaporator is crystallized to allow the preparation of a crystallized vanillin having a purity greater than or equal to 99.9% and having a color in ethanolic solution at 10% by weight less than or equal to 150 Hazen, preferably less than or equal to 100 Hazen, and very preferably less than or equal to 50 Hazen.
Selon un troisième mode de réalisation, représenté par la figure 1, le moût de fermentation est soumis à une étape de stabilisation par abaissement de la température à 21°C, ajustement du pH à 6,8, et ajout d'un adjuvant ou une pasteurisation à 60°C pendant 20 min. Un solvant organique est ajouté simultanément pour permettre d'extraire la vanilline en solution organique. La séparation de la biomasse et des phases aqueuse et organique est effectuée à l'aide d'un extracteur à contre-courant. La phase organique est alors soumise à une concentration par distillation sous vide. Le solvant organique évaporé peut être recyclé dans l'étape de séparation de la biomasse. La vanilline est alors soumise à une deuxième étape d'évaporation, de préférence dans un évaporateur à film raclé de manière à séparer la vanilline et les lourds. La vanilline est récupérée en tête de l'évaporateur avec d'éventuelles impuretés telles que l'alcool vanillique. Enfin ce flux récupéré en tête d'évaporateur est cristallisé pour permettre la préparation d'une vanilline cristallisée ayant une pureté supérieure ou égale à 99,9% et ayant une
couleur en solution éthanolique à 10% en poids inférieure ou égale à 150 Hazen, de préférence inférieure ou égale à 100 Hazen, et très préférentiellement inférieur ou égale à 50 Hazen. According to a third embodiment, represented by FIG. 1, the fermentation must is subjected to a stabilization step by lowering the temperature to 21° C., adjusting the pH to 6.8, and adding an adjuvant or a pasteurization at 60°C for 20 min. An organic solvent is added simultaneously to allow the vanillin to be extracted in organic solution. The separation of the biomass and the aqueous and organic phases is carried out using a counter-current extractor. The organic phase is then subjected to concentration by vacuum distillation. The evaporated organic solvent can be recycled to the biomass separation step. The vanillin is then subjected to a second stage of evaporation, preferably in a wiped film evaporator so as to separate the vanillin and the heavies. The vanillin is recovered at the top of the evaporator with any impurities such as vanillic alcohol. Finally, this stream recovered at the top of the evaporator is crystallized to allow the preparation of a crystallized vanillin having a purity greater than or equal to 99.9% and having a color in 10% by weight ethanol solution less than or equal to 150 Hazen, preferably less than or equal to 100 Hazen, and very preferably less than or equal to 50 Hazen.
Selon un quatrième mode de réalisation, représenté par la figure 1, le moût de fermentation est soumis à une étape de stabilisation. Ce moût de fermentation stabilisé est agité avec ajout simultané d'un solvant organique. Ce mélange est alors séparé en employant un décanteur centrifuge. La phase organique est alors soumise à une concentration par distillation sous vide en continu ou discontinu. Le solvant organique évaporé peut être recyclé dans l'étape de séparation de la biomasse. La vanilline est alors soumise à une deuxième étape d'évaporation, de préférence dans un évaporateur à film raclé de manière à séparer la vanilline et les lourds. La vanilline est récupérée en tête de l'évaporateur avec d'éventuelles impuretés telles que l'alcool vanillique. Enfin ce flux récupéré en tête d'évaporateur est cristallisé pour permettre la préparation d'une vanilline cristallisée ayant une pureté supérieure ou égale à 99,9% et ayant une couleur en solution éthanolique à 10% en poids inférieure ou égale à 150 Hazen, de préférence inférieure ou égale à 100 Hazen, et très préférentiellement inférieur ou égale à 50 Hazen.According to a fourth embodiment, represented by FIG. 1, the fermentation broth is subjected to a stabilization step. This stabilized fermentation broth is stirred with the simultaneous addition of an organic solvent. This mixture is then separated using a centrifugal decanter. The organic phase is then subjected to concentration by continuous or discontinuous vacuum distillation. The evaporated organic solvent can be recycled to the biomass separation step. The vanillin is then subjected to a second stage of evaporation, preferably in a wiped film evaporator so as to separate the vanillin and the heavies. The vanillin is recovered at the top of the evaporator with any impurities such as vanillic alcohol. Finally, this stream recovered at the head of the evaporator is crystallized to allow the preparation of a crystallized vanillin having a purity greater than or equal to 99.9% and having a color in ethanolic solution at 10% by weight less than or equal to 150 Hazen, preferably less than or equal to 100 Hazen, and very preferably less than or equal to 50 Hazen.
Selon un cinquième mode de réalisation, représenté par la figure 2, le moût de fermentation est soumis à une étape de stabilisation. Ce moût de fermentation stabilisé est filtré permettant la séparation de la biomasse. La filtration est effectuée par microfiltration suivie d'une nanofiltration. Un solvant organique est ensuite ajouté pour permettre d'extraire la vanilline en solution organique, les phases aqueuses et organiques sont séparées par extraction en continu. La phase organique est alors soumise à une concentration par distillation sous vide en continu ou discontinu. Le solvant organique évaporé peut être recyclé dans l'étape de séparation de la biomasse. La vanilline est alors soumise à une deuxième étape d'évaporation, de préférence dans un évaporateur à film raclé de manière à séparer la vanilline et les lourds. La vanilline est récupérée en tête de l'évaporateur avec d'éventuelles impuretés telles que l'alcool vanillique. Enfin ce flux récupéré en tête d'évaporateur est cristallisé pour permettre la préparation d'une vanilline cristallisée ayant une pureté supérieure ou égale à 99,9% et ayant une couleur en solution éthanolique à 10% en poids inférieure ou égale à 150 Hazen, de préférence inférieure ou égale à 100 Hazen, et très préférentiellement inférieur ou égale à 50 Hazen. According to a fifth embodiment, represented by FIG. 2, the fermentation broth is subjected to a stabilization step. This stabilized fermentation must is filtered allowing the separation of the biomass. Filtration is carried out by microfiltration followed by nanofiltration. An organic solvent is then added to make it possible to extract the vanillin in organic solution, the aqueous and organic phases are separated by continuous extraction. The organic phase is then subjected to concentration by continuous or discontinuous vacuum distillation. The evaporated organic solvent can be recycled to the biomass separation step. The vanillin is then subjected to a second stage of evaporation, preferably in a wiped film evaporator so as to separate the vanillin and the heavies. The vanillin is recovered at the top of the evaporator with any impurities such as vanillic alcohol. Finally, this stream recovered at the head of the evaporator is crystallized to allow the preparation of a crystallized vanillin having a purity greater than or equal to 99.9% and having a color in ethanolic solution at 10% by weight less than or equal to 150 Hazen, preferably less than or equal to 100 Hazen, and very preferably less than or equal to 50 Hazen.
Selon un sixième mode de réalisation, représenté par la figure 2, le moût de fermentation est soumis à une étape de stabilisation. Ce moût de fermentation stabilisé est filtré permettant la séparation de la biomasse par filtration frontale. Un solvant organique est ensuite ajouté pour permettre d'extraire la vanilline en solution organique, les phases aqueuses et organiques sont séparées par extraction en continu. La phase organique est alors soumise à une concentration par distillation sous vide en continu ou discontinu. Le solvant organique évaporé peut être recyclé dans l'étape de séparation de la biomasse. La vanilline est alors soumise à une deuxième étape d'évaporation, de préférence dans un évaporateur à film raclé de manière à séparer la vanilline et les lourds. La vanilline est récupérée en tête de l'évaporateur avec d'éventuelles impuretés telles que l'alcool vanillique. Enfin ce flux récupéré en tête d'évaporateur est cristallisé pour permettre la préparation d'une vanilline cristallisée ayant une pureté supérieure ou égale à 99,9% et ayant une couleur en solution éthanolique à 10% en poids inférieure ou égale à 150 Hazen, de préférence inférieure ou égale à 100 Hazen, et très préférentiellement inférieur ou égale à 50 Hazen. According to a sixth embodiment, shown in Figure 2, the fermentation broth is subjected to a stabilization step. This stabilized fermentation must is filtered allowing the separation of the biomass by frontal filtration. An organic solvent is then added to make it possible to extract the vanillin in organic solution, the aqueous and organic phases are separated by continuous extraction. The organic phase is then subjected to concentration by continuous or discontinuous vacuum distillation. The evaporated organic solvent can be recycled to the biomass separation step. The vanillin is then subjected to a second stage of evaporation, preferably in a wiped film evaporator so as to separate the vanillin and the heavies. The vanillin is recovered at the top of the evaporator with any impurities such as vanillic alcohol. Finally, this stream recovered at the head of the evaporator is crystallized to allow the preparation of a crystallized vanillin having a purity greater than or equal to 99.9% and having a color in ethanolic solution at 10% by weight less than or equal to 150 Hazen, preferably less than or equal to 100 Hazen, and very preferably less than or equal to 50 Hazen.
Selon un septième mode de réalisation représenté par la figure 3, le moût de fermentation est stabilisé et précipité. Une étape de séparation solide/liquide est ensuite réalisée de manière à séparer le gâteau comprenant la vanilline et la biomasse d'une phase aqueuse liquide comprenant certaines impuretés du
procédé de fermentation. La vanilline contenue dans le gâteau est ensuite solubilisée avec un solvant organique ou de l'eau pour permettre la séparation d'une phase liquide aqueuse ou organique comprenant la vanilline de la biomasse. La phase liquide aqueuse ou organique comprenant la vanilline est ensuite soumise à des étapes de concentration, séparation des lourds et cristallisation telles que décrites dans le premier mode de réalisation. According to a seventh embodiment represented by FIG. 3, the fermentation broth is stabilized and precipitated. A solid/liquid separation step is then carried out so as to separate the cake comprising the vanillin and the biomass from a liquid aqueous phase comprising certain impurities of the fermentation process. The vanillin contained in the cake is then dissolved with an organic solvent or water to allow the separation of an aqueous or organic liquid phase comprising the vanillin from the biomass. The aqueous or organic liquid phase comprising the vanillin is then subjected to steps of concentration, separation of heavy substances and crystallization as described in the first embodiment.
Selon un huitième mode de réalisation, représenté par la figure 4, le moût de fermentation est stabilisé. Une étape de séparation solide/liquide est ensuite réalisée de manière à séparer le gâteau comprenant la biomasse d'une phase aqueuse liquide comprenant la vanilline. La séparation solide/liquide peut être effectuée par n'importe quelle méthode décrite selon les modes de réalisations 1 à 6. La phase liquide aqueuse est alors soumise à une étape d'adsorption sur résine ou de pertraction avec ajout simultané d'un solvant organique. La phase organique comprenant la vanilline est ensuite soumise à des étapes de concentration, séparation des lourds et cristallisation telles que décrites dans le premier mode de réalisation. According to an eighth embodiment, represented by FIG. 4, the fermentation broth is stabilized. A solid/liquid separation step is then carried out so as to separate the cake comprising the biomass from a liquid aqueous phase comprising the vanillin. The solid/liquid separation can be carried out by any method described according to embodiments 1 to 6. The aqueous liquid phase is then subjected to a step of adsorption on resin or pertraction with simultaneous addition of an organic solvent. . The organic phase comprising the vanillin is then subjected to steps of concentration, separation of heavy substances and crystallization as described in the first embodiment.
Selon un neuvième mode de réalisation, représenté par la figure 5, le moût de fermentation est stabilisé. Une étape de séparation solide/liquide est ensuite réalisée de manière à séparer la biomasse, de préférence cette séparation est conduite par microfiltration ou diafiltration. Cette première séparation peut être suivie d'une étape d'ultrafiltration. Cette ultrafiltration permet en particulier de séparer des particules non séparées lors de la séparation sur membrane céramique. L'ultrafiltrat est ensuite soumis à une étape de nanofiltration (ou éventuellement d'osmose inverse) afin de concentrer le flux en vanilline. Ce flux de vanilline est ensuite soumis à une étape de cristallisation dans un solvant eau/alcool telle que décrite précédemment. According to a ninth embodiment, represented by FIG. 5, the fermentation broth is stabilized. A solid/liquid separation stage is then carried out so as to separate the biomass, preferably this separation is carried out by microfiltration or diafiltration. This first separation can be followed by an ultrafiltration step. This ultrafiltration makes it possible in particular to separate particles not separated during the separation on a ceramic membrane. The ultrafiltrate is then subjected to a nanofiltration step (or optionally reverse osmosis) in order to concentrate the flux in vanillin. This vanillin stream is then subjected to a crystallization step in a water/alcohol solvent as described previously.
Exemples Examples
Une composition telle que définie dans le tableau 1 est soumise à une cristallisation dans un mélange eau/éthanol, dans lequel la teneur est éthanol est comprise entre 15 et 25% en masse. La cristallisation est conduite par refroidissement de 40°C à 4°C. La concentration en vanilline en début de cristallisation est comprise entre 15 et 25% en masse. A composition as defined in Table 1 is subjected to crystallization from a water/ethanol mixture, in which the ethanol content is between 15 and 25% by weight. Crystallization is carried out by cooling from 40°C to 4°C. The vanillin concentration at the start of crystallization is between 15 and 25% by weight.
Tableau 1
Table 1
Après cristallisation, la vanilline cristallisée est filtrée, lavée à l'eau, séchée et analysée. La vanilline cristallisée présente une pureté de 99,6% La teneur en alcool vanillique est de 0,04%. La teneur en acide vanillique est de 0,01%. After crystallization, the crystallized vanillin is filtered, washed with water, dried and analyzed. Crystallized vanillin has a purity of 99.6%. Vanillic alcohol content is 0.04%. The vanillic acid content is 0.01%.
Avantageusement, le rendement global en vanilline lors de la cristallisation est de 94% sans recycle du filtrat de la cristallisation.
Exemple 2 (Comparatif) Advantageously, the overall vanillin yield during the crystallization is 94% without recycling the crystallization filtrate. Example 2 (Comparative)
Une composition telle que définie dans le tableau 1 est soumise à une évaporation sous vide. A composition as defined in Table 1 is subjected to vacuum evaporation.
Exemple 2.1: Example 2.1:
Après évaporation, en mode batch, la vanilline purifiée est analysée. La vanilline purifiée présente une pureté de 99,7%. La teneur en alcool vanillique est inférieure à 0,01%. La teneur en acide vanillique est inférieure à 0,01%. After evaporation, in batch mode, the purified vanillin is analyzed. Purified vanillin has a purity of 99.7%. Vanilla alcohol content is less than 0.01%. The vanillic acid content is less than 0.01%.
Cependant, le rendement global de la vanilline obtenue dans le cadre de l'exemple 2.1 n'est que de 70%. However, the overall yield of the vanillin obtained in the context of Example 2.1 is only 70%.
Exemple 2.2: Après évaporation, en mode continu, la vanilline purifiée est analysée. Example 2.2: After evaporation, in continuous mode, the purified vanillin is analyzed.
Le rendement global de la vanilline obtenue dans le cadre de l'exemple 2.2 est de 95%. Cependant, La vanilline purifiée présente une pureté de 98%. La teneur en alcool vanillique est de 1%. La teneur en acide vanillique est inférieure à 0,01%. The overall yield of the vanillin obtained in the context of Example 2.2 is 95%. However, purified vanillin has a purity of 98%. The vanilla alcohol content is 1%. The vanillic acid content is less than 0.01%.
Le procédé de la présente invention permet avantageusement d'obtenir de la vanilline ayant de bonnes caractéristiques de pureté et avec de très bons rendements.
The process of the present invention advantageously makes it possible to obtain vanillin having good purity characteristics and with very good yields.
Claims
1. Procédé de purification de vanilline ou ses dérivés, obtenus par un procédé biotechnologique, comprenant au moins une étape dans laquelle la vanilline ou ses dérivés sont séparés de l'alcool vanillique ou ses dérivés par cristallisation. 1. Process for the purification of vanillin or its derivatives, obtained by a biotechnological process, comprising at least one stage in which the vanillin or its derivatives are separated from the vanillic alcohol or its derivatives by crystallization.
2. Procédé selon la revendication 1 caractérisé en ce que la cristallisation est effectuée dans un mélange eau/alcool, de préférence la quantité d'alcool est comprise entre 2% et 40% en poids. 2. Method according to claim 1 characterized in that the crystallization is carried out in a water / alcohol mixture, preferably the amount of alcohol is between 2% and 40% by weight.
3. Procédé selon l'une quelconque des revendication 1 à 2 caractérisé en ce qu'il comprend en outre au moins une étape de stabilisation d'un moût de fermentation comprenant de la vanilline ou ses dérivés obtenus par un procédé biotechnologique. 3. Method according to any one of claims 1 to 2 characterized in that it further comprises at least one step of stabilizing a fermentation broth comprising vanillin or its derivatives obtained by a biotechnological process.
4. Procédé selon l'une quelconque des revendications 1 à 3 caractérisé en ce qu'il comprend en outre au moins une étape de séparation de la biomasse. 4. Method according to any one of claims 1 to 3 characterized in that it further comprises at least one biomass separation step.
5. Procédé selon l'une quelconque des revendications 1 à 4 caractérisé en ce qu'il comprend en outre au moins une étape de concentration d'une solution aqueuse ou organique de vanilline ou ses dérivés. 5. Method according to any one of claims 1 to 4 characterized in that it further comprises at least one step of concentrating an aqueous or organic solution of vanillin or its derivatives.
6. Procédé selon l'une quelconque des revendications 1 à 5 caractérisé en ce qu'il comprend en outre au moins une étape dans laquelle la vanilline ou ses dérivés est séparée de composés ayant un point d'ébullition plus élevé que celui de la vanilline ou ses dérivés. 6. Method according to any one of claims 1 to 5 characterized in that it further comprises at least one step in which vanillin or its derivatives is separated from compounds having a higher boiling point than that of vanillin or its derivatives.
7. Procédé selon l'une quelconque des revendications 1 à 6 dans lequel la vanilline ou ses dérivés obtenus à l'issue de l'étape de cristallisation présentent une couleur en solution éthanolique à 10% en poids inférieure ou égale à 150 Hazen, de préférence inférieure ou égale à 100 Hazen, et très préférentiellement inférieure ou égale à 50 Hazen.
7. Process according to any one of claims 1 to 6, in which the vanillin or its derivatives obtained at the end of the crystallization step have a color in 10% by weight ethanolic solution of less than or equal to 150 Hazen, of preferably less than or equal to 100 Hazen, and very preferably less than or equal to 50 Hazen.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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FR2102534A FR3120629B1 (en) | 2021-03-15 | 2021-03-15 | Process for purifying vanillin or a vanillin derivative obtained by a biotechnological process |
PCT/EP2022/056527 WO2022194771A1 (en) | 2021-03-15 | 2022-03-14 | Process for the purification of vanillin or a vanillin derivative obtained by a biotechnological process |
Publications (1)
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EP4308534A1 true EP4308534A1 (en) | 2024-01-24 |
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Application Number | Title | Priority Date | Filing Date |
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EP22714200.7A Pending EP4308534A1 (en) | 2021-03-15 | 2022-03-14 | Process for the purification of vanillin or a vanillin derivative obtained by a biotechnological process |
Country Status (6)
Country | Link |
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US (1) | US20240190801A1 (en) |
EP (1) | EP4308534A1 (en) |
CN (1) | CN117098747A (en) |
BR (1) | BR112023018030A2 (en) |
FR (1) | FR3120629B1 (en) |
WO (1) | WO2022194771A1 (en) |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2745796A (en) | 1953-10-21 | 1956-05-15 | Aschaffenburger Zellstoffwerke | Method of recovering vanillin |
DE1132113B (en) | 1959-07-09 | 1962-06-28 | Aschaffenburger Zellstoffwerke | Method of purifying vanillin |
DE3920039A1 (en) | 1989-06-20 | 1991-01-03 | Haarmann & Reimer Gmbh | METHOD FOR PRODUCING NATURAL VANILLIN |
CA2238215A1 (en) | 1997-06-19 | 1998-12-19 | Markus Wetli | Process for the production of vanillin |
BR112014003041B1 (en) | 2011-08-08 | 2021-10-13 | International Flavors & Fragrances Inc. | METHOD FOR PRODUCING BETA-D-GLYCOSIDE VANILIN AND/OR VANILIN, MUTANT CATECHOL-OMETYL TRANSFERASE (COMT) POLYPEPTIDE, AND RECOMBINANT HOST MICROORGANISM |
FR2984314B1 (en) | 2011-12-15 | 2014-01-17 | Rhodia Operations | PROCESS FOR PURIFYING VANILLIN BY LIQUID-LIQUID EXTRACTION |
JP6579957B2 (en) | 2013-01-24 | 2019-09-25 | ローディア オペレーションズ | Purification method of natural vanillin |
FR3099477B1 (en) * | 2019-07-30 | 2023-01-13 | Rhodia Operations | Natural vanillin compositions |
-
2021
- 2021-03-15 FR FR2102534A patent/FR3120629B1/en active Active
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2022
- 2022-03-14 BR BR112023018030A patent/BR112023018030A2/en unknown
- 2022-03-14 US US18/550,801 patent/US20240190801A1/en active Pending
- 2022-03-14 EP EP22714200.7A patent/EP4308534A1/en active Pending
- 2022-03-14 CN CN202280021151.8A patent/CN117098747A/en active Pending
- 2022-03-14 WO PCT/EP2022/056527 patent/WO2022194771A1/en active Application Filing
Also Published As
Publication number | Publication date |
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WO2022194771A1 (en) | 2022-09-22 |
FR3120629B1 (en) | 2024-01-19 |
US20240190801A1 (en) | 2024-06-13 |
CN117098747A (en) | 2023-11-21 |
BR112023018030A2 (en) | 2023-10-03 |
FR3120629A1 (en) | 2022-09-16 |
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