Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
  • C07C51/42—Separation; Purification; Stabilisation; Use of additives
  • C07C51/43—Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation

Definitions

• the present invention relates to a process for purifying lactic acid so as to produce in a single crystallization step lactic acid crystals with a specific surface area ⁇ 0.05 m 2 / g.
• lactic acid or hydroxy-2-propanoic acid which is an ⁇ -hydroxy carboxylic acid can be produced by fermentation.
• Other routes for obtaining lactic acid are known to those skilled in the art, via chemical transformations of reagents derived from petrochemistry, such as the hydrolysis of lactonitrile, itself obtained from acetaldehyde, chlorination and hydrolysis of propionic acid or else by nitration of propene.
• lactic acid exists in two diastereoisomeric forms, the L (+) form and the D (-) form, and meets with new applications every day, from conventional use as a food preservative to new developments such as the synthesis of solvents, pesticides, herbicides, biodegradable polymers, ...
• the lactic acid must have a very high purity and a very low thermo-stability index, generally less than 50 Hazen, or in some cases less than 30. Hazen. It corresponds to a so-called "polymer” grade when it allows the production of a polylactic acid with a molecular weight greater than 100000 daltons as indicated in the patent (EP 1953 234 A1).
• thermostable lactic acid from a fermentation juice rich in lactic acid can be achieved by various technologies which generally comprise common steps:
• WO 0222545 has also described a method for purifying lactic acid, but which comprises, before the crystallization step, an organic solvent extraction step, instead of a distillation. It is known to those skilled in the art that a small percentage of organic extractant is found in the aqueous phase from this extraction, which requires an additional purification step to remove this solvent residue.
• the impure fermentation juice can be purified without the use of organic solvent.
• the purity of crystals is generally related to their specific surface area.
• the mass specific surface area (SSM) of crystals is the area developed by the crystals per unit weight.
• the specific surface area (SSM) makes it possible to compare the dimensional characteristics of crystals of a suspension or a powder with those of another suspension or powder. This specific surface can be measured by optical imaging based on the volume Vm and the average surface Sm of hundreds of crystals (by measurement of the length of their face) and the density of the crystals Dc:
• the amount of residual mother liquor per unit mass of crystals is proportional to the surface thereof.
• the impurities being mainly in the mother liquor, the less the surface developed by the crystals per unit of mass will be important and the less the mass of crystals will contain impurities. This is for example the case of sugar beet and cane.
• nucleation There are two types of nucleation, primary nucleation and secondary nucleation.
• nucleation In the case of a primary nucleation, the appearance of the germs is done in a medium where there is still no crystal of the phase which precipitates. If the germs are formed in the volume of the solution, the nucleation is called primary homogeneous. If, on the contrary, they form on the walls of the crystallizers, on the agitators or on solid particles floating in the solution, the nucleation is said to be heterogeneous primary.
• the nucleation temperature (Tn) mentioned in the present patent application corresponds to the secondary nucleation temperature.
• supersaturation S (g / 1) at a given temperature can be defined as the difference between the concentration in solution C (g / 1) and the saturation concentration C * (g / 1).
• Ts c is the solubilization temperature
• Tn c is the secondary nucleation temperature.
• the very structure of lactic acid carrying both a hydroxyl function and a carboxylic acid group is at the origin of condensation reactions generating lactoyllactic, dilactoyllactic, trilactoyllactic, ... (n-lactoyllactic) units. also called lactic acid oligomers. These condensation or oligomerization reactions tend towards equilibrium but are all the more likely that the concentration of the starting aqueous solution and the temperature are high (Holten CH., "Lactic Acid: Properties and Chemistry of Lactic Acid and Derivatives"). ", Verlag Chemie, 1971).
• the monomer content relative to the total lactic acid concentration can be estimated by the following equation provided that the total acidity is less than 105%:
• Relative monomer content (AT% - (AT% -AL%) * 2) / AT%
• AT total acidity determined by acid-base titration after saponification and expressed as lactic acid monomer
• AL free acidity determined by direct acid-base titration and expressed as lactic acid monomer
• the subject of the present invention is a process for purifying lactic acid making it possible to produce crystals with a specific surface area of less than 0.05 m 2 / g from an impure aqueous solution with a coloration greater than 500 Hazen.
• the subject of the present invention is also a process for purifying lactic acid by crystallization and preferably without distillation, making it possible to produce crystals with a mass surface area of ⁇ 0.05 m 2 / g, the content of other impurities being such that a solution aqueous 90% prepared from the crystals is grade thermostable and preferably coloring less than 30 Hazen after heating at 200 0 C for 2h.
• the present invention also relates to a process for purifying lactic acid by crystallization by controlling the oligomeric content of the solution and by controlling the supersaturation factor.
• the Applicant Company has developed a method for purifying lactic acid comprising a step of forming crystals having a specific surface area of less than 0.05 m 2 / g of crystals from a lactic acid solution with a coloration greater than 500 Hazen. and having a relative monomer content greater than 80% characterized in that: 1) The solution is cooled to a low degree of supersaturation
• crystallization should be carried out by controlling the temperature so as to maintain a degree of supersaturation of less than 60% and preferably of between 1 and 40%.
• the Applicant Company found that on the one hand the residual impurities not removed after crystallization were predominantly present in the surface impregnation liquid and on the other hand that the specific surface area of the crystals was strongly related to the value of supersaturation. Indeed, with low supersaturation, the crystals have a low surface density while at high supersaturation, the applicant company has observed a significant increase in lactic acid crystals (needle shape) with a consequent much larger crystalline surface.
• the Applicant Company has also unexpectedly found that by controlling the relative monomer content of the solution, i.e. keeping it above 80% and preferably above 90% could be affected. strongly crystallization by increasing the solubility temperature and the nucleation temperature and thus the crystallization yield. Indeed, it has been found that a decrease in the relative monomer level has a significant influence on the solubility and nucleation temperatures of lactic acid.
• the temperature is adjusted to 5 ° C below the theoretical solubility temperature.
• the temperature in the reactor is adjusted to 25 ° C (theoretical solubility temperature of 30 0 C for the chosen concentration and a product without oligomer).
• the temperature is then gradually increased until there are no more crystals.
• the temperature at which the last crystal disappears is the experimental solubility temperature.
• the solution is cooled according to a cooling ramp of 10 ° C / h.
• the nucleation temperature is measured when the first crystal (excluding crystals in solution) appears.
• Figure 1 shows the evolution of Tn and Ts as a function of the relative monomer content of a lactic acid having an AT of 89%. It is clear from Table 1 and Figure 1 that a decrease in the relative monomer level has a significant influence on solubility and nucleation temperatures of lactic acid.
• the applicant company has surprisingly found that it is preferable to use a starting lactic acid solution of between 85 and 95% of total acidity and preferably of between 88 and 93% of total acidity and exhibiting relative monomer content greater than 80% and preferably between 90 and 100% to obtain after purification according to the method of the invention crystals having the desired properties.
• the lactic acid solution with a coloration greater than 500 Hazen preferably originates from a prepurified fermentation juice, for example by conventional filtration and / or membrane filtration, by passage over ion exchange resins and / or over activated carbons, and concentrated. by the techniques known to those skilled in the art to the desired title but may also come from any other source of lactic acid such as, in a non-limiting manner, lactic acid production wastes or recycling of lactic acid. poly-lactic acid after hydrolysis.
• the crystallization in itself and outside the control performed on the oligomerization and supersaturation can be carried out by any crystallization technology known to those skilled in the art such as those described in the techniques of the Engineer "Industrial Crystallization” Practical aspects 2 788), such as scraped crystallizers, stirred crystallizers, adiabatic evaporative crystallizers, classification crystallizers (such as DTP Swenson type, DP Tsukishima and Turbulence Messo), fluidized bed crystallizers (such as Oslo or Krystal type), forced circulation crystallizers, direct contact cooling crystallizers, multi-stage multi-stage crystallizers.
• any crystallization technology known to those skilled in the art such as those described in the techniques of the Engineer "Industrial Crystallization” Practical aspects 2 788
• scraped crystallizers such as scraped crystallizers, stirred crystallizers, adiabatic evaporative crystallizers, classification crystallizers (such as DTP Swenson type, DP Tsukishim
• this step can also be carried out by crystallization technologies from a molten medium (such as those of Kobe Steel, Proabd, Sulzer, Phillips, Brodie brands, for example). , 4C Tsukishima, TNO, Brenband, Niro).
• the separation of crystals and mother liquor can be carried out by any of the techniques known to those skilled in the art, such as for example described in Perry's Chemical Engineers' Handbook, chapter 8 (decantation, filtration, centrifugation, spin, washing column).
• the mother liquor recovered during liquid / solid separation can be recycled downstream of the crystallization to ensure a higher overall yield.
• the crystals can also be washed, and in this case the washing of the crystals will be performed using a solution of lactate, lactic acid or water, or by washing the crystal cake during the step of solid-liquid separation either by resuspension of crystals followed by separation of crystals-wash solution.
• the washing solution will preferably be a lactic acid solution saturated or slightly unsaturated so as to cause a slight "wiping" of the crystals during washing. In the latter case, the washing will be preferably by controlling the temperature so as to control "wiping" while avoiding excessive loss of the crystal mass.
• the lactic acid crystals can be redissolved in water.
• the lactic acid solution may be bleached and purified for example on activated charcoal or by any techniques known to those skilled in the art to purify or decolorize lactic acid (membrane, ion exchange resins, adsorbent resins, treatment electrochemical (reduction, oxidation), ).
• the filtrate recovered during the liquid / solid separation can be recycled downstream of the crystallization to ensure a higher overall yield.
• One kilogram of lactic acid from filtered fermentation juice, pre-purified on ion exchange resins and activated charcoal, 99% concentrated and 2000 Hazen color, 96% relative monomer content and diluted at a lactic acid concentration of 92% is introduced into a finely thermostated reactor 51 provided with a propeller-shaped stirring blade.
• solubility and secondary nucleation temperatures measured according to the protocol described in the state of the art are respectively 26 ° C. and 18 ° C.
• the temperature of the solution is set according to the level of supersaturation and the solution is seeded with 20 g of lactic acid crystals.
• the solutions are gradually cooled according to a cooling ramp of 3 ° C / h to avoid nucleation even at high supersaturation for 5 hours.
• the temperatures are then respectively 10 and 4 ° C and maintained for 19 hours to let the crystals grow.
• the crystal size measurements were performed using an optical microscope (Askania RME5) equipped with a digital camera (Nikon Coolpix 4500) equipped with Leica-supplied crystal measuring software. For both conditions tested, the length (L1) and thickness (L2) of 200 crystals were measured.
• the specific surface area of the crystals obtained with low supersaturation is 0.03 m 2 / g whereas that of the crystals with high supersaturation is 0.06 m 2 / g. This is calculated by taking the surface and the volume of a parallelepiped of length L1 and width and thickness L2. The density of lactic acid in crystal form is estimated at 1.22 g / ml.
• the solution is gradually cooled according to a cooling ramp of 3 ° C / h to avoid nucleation even at high supersaturation for 5 hours.
• the temperatures are respectively 9 and 4 ° C and maintained for 19 hours to allow the crystals to grow.
• the 90% lactic acid solution obtained after washing and suspending the crystals is also brought into contact with 20 g / l of Norit ROX active carbon overnight at room temperature in a closed bottle on an orbital shaker.
• the solution is filtered and analyzed.
• the analyzes carried out on the 90% crystal solutions are a measurement of the coloring at room temperature (APHA scale in Hazen units) and a thermal stability test consisting in measuring the color (APHA scale in Hazen units) of the product after heating at room temperature. reflux at a temperature of 200 0 C for two hours.
• the specific surface area of the crystals is also estimated by measuring the length and the thickness of 200 crystals of each sample according to the protocol described in Example 1.
• the comparison of the results (table 5) indicates that the solution obtained from the purified crystals with low supersaturation has a high purity and is thermostable ( ⁇ 30 Hazen after heating).
• the purified crystals with medium supersaturation deliver a lower quality solution but a treatment on charcoal makes it possible to obtain a thermostable quality ( ⁇ 50 Hazen after heating).
• the purified crystals with high supersaturation deliver a low quality non-thermostable solution even after treatment with charcoal.
• a polymerization test is carried out starting from the lactic acid produced in Example 2 (low supersaturation and after treatment with activated charcoal) in order to demonstrate its adequacy with the qualitative requirements required for the production of polylactic acid.
• the lactic acid obtained above (-250 g) is introduced into a stirred flask and heated to 160 ° C. In order to facilitate the rapid extraction of the volatile compound, the unit is gradually placed under vacuum, the pressure varying between atmospheric pressure and 150 mbar (absolute) for ⁇ 10h. Lactic acid polymerizes to form a prepolymer characterized by a molecular weight of 1500 daltons.
• the prepolymer obtained is introduced into a flask heated by a heating cap at 220-250 ° C. and stirred with a magnetic chip.
• a polymerization catalyst, tin octoate, is then introduced into the flask at a rate of 1% by weight relative to the amount of prepolymer introduced.
• the flask is surmounted by a reflux at 180-200 ° C. and then a condenser cooled to 80-100 ° C. and finally a condensate collection flask.
• the whole is put under vacuum between 10 and 20 mbar.
• the impure lactide collected in the condensate flask is purified twice by recrystallization in a 1: 1 ratio with toluene.
• the purified lactide crystals are recovered by filtration and dried under vacuum in a Rotavapor type apparatus.
• Residual acidity ⁇ 10 meq / kg - Water content: 40 ppm
• a small amount of the purified product obtained above (10gr) is introduced into a test tube under a nitrogen sweep (several tests were run in parallel). After melting the mixture (100 ° C.), a solution of tin octoate is added so as to respect a molar monomer / catalyst ratio of 4500. Once the solution is well homogenized, it is immersed in an oil bath whose temperature is maintained at 180 ° C.
• test tubes After one hour, the test tubes are removed from the oil bath, cooled and broken so as to recover very rigid and opaque polymers.
• the polymers obtained were analyzed by GPC in chloroform at 35 ° C. and Mn between 90,000 and 110,000 measured (the molecular masses determined on the basis of a polystyrene calibration (PS) are corrected on an absolute basis using a universal calibration. as described by HA Andreetta, IH Sorokin, RV Figini, (1985) Absolute calibration method for liquid chromatography exclusion (GPC), Theoretical basis and methodology Die Makromolekulare Chemie, Rapid Communications, Volume 6, Issue 6, Pages 419-423)) which demonstrate the possibility of satisfactorily polymerizing purified lactic acid according to the proposed process
• Example 4 Impact of the lactic acid concentration on the productivity and the quality of the crystals
• the lactic acid concentration of the starting solution is ⁇ 95% and preferably between 85 and 95%. Indeed, as shown in the example below when the concentration of the starting solution is> 95%, there is a drastic decrease in the quality and productivity of lactic acid crystals, all other parameters remaining in the defined conditions of the process of the invention
• the solution is gradually cooled according to a cooling ramp of 3 ° C / h to avoid nucleation even at high supersaturation for 5 hours.
• the temperature is then 26 ° C.
• Half of the suspension is directly treated on wringer as described in Example 2 (crystals 4.a), while the other half is maintained at 26 ° C. for 19h (crystals 4.b) before being also treated identically.
• the 90% lactic acid solution obtained after washing and suspending the crystals is also brought into contact with 20 g / l of Norit ROX active carbon overnight at room temperature in a closed bottle on an orbital shaker.
• the solution is filtered and analyzed.
• Tables 7 and 8 show the poor quality of the lactic acid crystals produced by the process described in this invention when the starting solution has a concentration greater than 95% lactic acid. This quality improves by letting the crystals ripen for 19 hours but the productivity drops sharply.
• the present invention will therefore be applied preferentially to starting solutions with a concentration of less than or equal to 95%.

Landscapes

• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Crystallography & Structural Chemistry (AREA)
• Engineering & Computer Science (AREA)
• Oil, Petroleum & Natural Gas (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
• Preparation Of Compounds By Using Micro-Organisms (AREA)
• Polyesters Or Polycarbonates (AREA)

Applications Claiming Priority (2)

Publications (1)

Family

ID=40822909

Family Applications (1)

Country Status (6)

Families Citing this family (7)

Family Cites Families (8)

• 2008
  • 2008-12-24 BE BE2008/0702A patent/BE1018561A3/fr active
• 2009
  • 2009-11-18 BR BRPI0923650A patent/BRPI0923650A2/pt not_active IP Right Cessation
  • 2009-11-18 WO PCT/EP2009/065385 patent/WO2010072473A1/fr active Application Filing
  • 2009-11-18 EP EP09752839A patent/EP2376418A1/de not_active Withdrawn
  • 2009-11-18 CN CN200980147359.9A patent/CN102227399A/zh active Pending
  • 2009-11-18 US US13/141,920 patent/US8471062B2/en not_active Expired - Fee Related

Non-Patent Citations (1)

Also Published As

Similar Documents

Legal Events