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
  • C07C45/51—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
  • C07C45/52—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition by dehydration and rearrangement involving two hydroxy groups in the same molecule
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
  • C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
  • C07C51/21—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
  • C07C51/23—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of oxygen-containing groups to carboxyl groups
  • C07C51/235—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of oxygen-containing groups to carboxyl groups of —CHO groups or primary alcohol groups
• • 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
• • 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
  • C07C51/44—Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation by distillation
• • 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
  • C07C51/48—Separation; Purification; Stabilisation; Use of additives by liquid-liquid treatment
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
  • C07C57/02—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms with only carbon-to-carbon double bonds as unsaturation
  • C07C57/03—Monocarboxylic acids
  • C07C57/04—Acrylic acid; Methacrylic acid

Definitions

• the present invention relates to a process for producing a bio-resourced acrylic acid from glycerol as raw material, the term bio-resoured acid indicating that the acrylic acid is essentially based on a source of carbon of natural origin.
• Acrylic acid is a very important raw material that can be used directly to obtain an acrylic acid polymer or, after esterification with alcohols, to produce a polymer of the corresponding ester.
• These polymers are used as such or as copolymers in fields as varied as hygiene (for example in the production of superabsorbents), detergents, paints, varnishes, adhesives, paper, textiles, leather , etc. ...
• Industrialists have been developing processes for the synthesis of acrylic acid for decades.
• a first generation used acetylenic-type triple bond compounds as raw material, which was reacted with a mixture of carbon monoxide and water in the presence of a nickel-based catalyst.
• Methanolysis of vegetable oils or animal fats can be carried out according to various well-known methods, in particular by using homogeneous catalysis such as sodium hydroxide or sodium methylate in solution in methanol, or by using heterogeneous catalysis.
• homogeneous catalysis such as sodium hydroxide or sodium methylate in solution in methanol
• heterogeneous catalysis we can refer to this topic in the article by D. Ballerini et al. in the Chemical News of nov-dec 2002.
• Patent applications EP 1.710.227, WO2006 / 136336 and WO2006 / 092272 describe such processes for synthesizing acrylic acid from glycerol comprising the step of dehydration in the gas phase in the presence of catalysts consisting of inorganic oxides (mixed or not) based on aluminum, titanium, zirconium, vanadium, etc., and the step of gas phase oxidation of acrolein thus synthesized in the presence of catalysts based on iron oxides, molybdenum, copper, alone or in combination in the form of mixed oxides.
• catalysts consisting of inorganic oxides (mixed or not) based on aluminum, titanium, zirconium, vanadium, etc.
• Acrylic acid is intended for the implementation by the industrialists of polymerization processes either of acrylic acid or of its ester derivatives, processes which are conducted in various forms in bulk, in solution, in suspension, in emulsion. These processes can be very sensitive to the presence in the feed of certain impurities, such as aldehydes or unsaturated compounds, which can sometimes prevent the expected use value from being obtained, for example by limiting the conversion of monomer to polymer, limiting the chain length of the polymer or interfering in the polymerization in the case of unsaturated compounds.
• impurities such as aldehydes or unsaturated compounds
• the reactor outlet effluent is subjected to a combination of stages which may differ by their sequence according to the process: elimination of incondensables and of the essential of the very compounds light, especially acrylic acrolein intermediate synthesis (AA crude), dehydration removing water and formaldehyde (AA dehydrated), elimination of light (especially acetic acid), elimination of heavy, possibly elimination of some residual impurities by chemical treatment.
• the invention relates to a process for manufacturing a "standard" acrylic acid using glycerol as raw material which will be converted into two stages - dehydration and oxidation - as mentioned previously integrated into a global purification process.
• This process has a great analogy with the synthesis process from propylene in that the intermediate product, acrolein, from the first step is the same and the second step is conducted under the same operating conditions.
• the first-stage reaction of the process of the invention dehydration reaction, is different from the propylene oxidation reaction of the usual process.
• the dehydration reaction conducted in the gas phase is carried out using solid catalysts different from those used for the oxidation of propylene.
• the acrolein-rich effluent from the first dehydration stage intended to supply the second acrolein oxidation step to acrylic acid, contains a larger quantity of water, and furthermore has significant differences in terms of byproducts resulting from the reaction mechanisms involved being concretized by different selectivities in each of the two pathways.
• Table 1 summarizes the data concerning the presence of various acids in the crude acrylic acid that is to say in the liquid phase leaving the second stage reactor.
• the impurity / AA ratios depend on the catalysts used, their "age” (degradation of the selectivities over time) and the operating conditions.
• the ratio 2-butenoic acid / AA is mentioned ⁇ 0.001% for the ex-propylene process; however, although the Applicant has never detected it in the AA-propylene, it deems it preferable to write " ⁇ 10 ppm" rather than 0% (result of its analyzes) in order to overcome the problem of detection threshold related to the method of analysis.
• Table 1 illustrates some of the main differences, in terms of the constituents of the liquid effluent leaving the oxidation reactor, between the ex-propylene and ex-glycerol processes.
• Table 1 illustrates some of the main differences, in terms of the constituents of the liquid effluent leaving the oxidation reactor, between the ex-propylene and ex-glycerol processes.
• it is also found in crude acrylic acid, that it comes from the ex-propylene process or the ex-glycerol process a whole series of oxygenates, alcohols, aldehydes, ketones , other acids, etc., whose separation, necessary, is known to those skilled in the art.
• the specifications for acrylic acid grades commonly used for the production of acrylic acid and acrylic ester polymers require that the levels of the impurities in Table 1 in acrylic acid be reduced to the values shown in Table 2 below. -Dessous.
• Acetic acid and propionic acid are troublesome in particular because they are not converted during the polymerization process, they are saturated and therefore not polymerizable; depending on the polymerization process involved and the targeted applications for the polymer, these impurities can remain in the finished product and risk giving the finished product undesirable corrosive properties, or be found in the liquid or gaseous discharges generated by the polymerization process and cause organic pollution also undesirable.
• 2-butenoic acid not synthesized by the ex-propylene process but present in its two configurations (E, also called crotonic acid, CAS No. 107-93-7) and (Z, also called isocrotonic acid, No. CAS: 503-64-0) in the ex-glycerol process, is particularly troublesome because, because of its double bond, it is likely to come into play in the polymerization process and thus to modify the characteristics and the use value of the final polymer.
• E also called crotonic acid, CAS No. 107-93-7
• Z also called isocrotonic acid, No. CAS: 503-64-0
• the problem is that of obtaining an acrylic acid of a degree of purity corresponding to the needs of the users and in particular meeting the specifications given in Table 2 by implementing a process for the synthesis of acrylic acid using the glycerol as raw material which has the disadvantage, compared to the conventional propylene oxidation process, of providing at the outlet of the oxidation reactor a gaseous mixture containing a lot of water and having contents important in various impurities such as acetic acid, propionic and 2-butenoic.
• the Applicant has discovered that it is possible to overcome the above disadvantages by implementing a process for purifying the gaseous effluent from the oxidation reactor of a process for synthesizing acrylic acid from glycerol, comprising a first step of dehydration of glycerol followed by a second step of oxidation of acrolein, conjugating a step of absorbing acrylic acid with a heavy solvent at the outlet of the oxidation reactor and a purification phase with several steps ending in a separation of acrylic acid by fractional crystallization.
• the subject of the invention is a process for producing bio-resourced acrylic acid from glycerol comprising the following steps:
• step (3) the liquid phase resulting from step (3) is subjected to
• step 4 a distillation top with separation at the top of the water and residual light (step 4), the bottoms fraction being sent to step (5),
• step 5 a distillation of the acrylic acid solution thus obtained to separate the heavy solvent at the bottom and at the top the acrylic acid fraction containing the intermediate impurities and possibly traces of solvent (step 5)
• Glycerol is a chemical, 1,2,3-propane triol, which can be obtained either by chemical synthesis from propylene, or as a co-product formed during the methanolysis of vegetable oils or animal fats.
• Methanolysis of vegetable oils or animal fats can be carried out according to various well-known methods, in particular by using homogeneous catalysis such as sodium hydroxide or sodium methylate in solution in methanol, or by using heterogeneous catalysis.
• homogeneous catalysis such as sodium hydroxide or sodium methylate in solution in methanol
• heterogeneous catalysis we can refer to this topic in the article by D. Ballerini et al. in the Chemical News of nov-dec 2002.
• Methyl esters are used in particular as fuels or fuels in diesel and heating oil.
• VOME methyl esters of oils vegetable
• the production of glycerol according to this route of production increases sharply, the glycerol representing about 10% of the weight of the processed oil.
• Glycerin the name of glycerol when it is in aqueous solution, obtained from vegetable oils or animal fats may contain salts (NaCl, Na 2 SO 4 , KCl, K 2 SO 4 ).
• a stream feeding the reactor of step (1) containing glycerol and water is generally used, with a water / glycerol mass ratio that can vary widely, for example between 0 , 04/1 and 9/1 and preferably between 0.7 / 1 and 3/1.
• the process is carried out in two distinct steps with two different catalysts.
• the dehydration reaction, step (1) which is a reaction balanced but favored by a high temperature level, is generally carried out in the gas phase in the reactor in the presence of a catalyst at a temperature ranging from 150 ° C. to 500 ° C. 0 C, preferably between 250 0 C and 350 0 C, and an absolute pressure between 1 and 5 bar (100 and 500 kPa). It can also be conducted in the liquid phase. It can also be carried out in the presence of oxygen or an oxygen-containing gas as described in applications WO 06/087083 and WO 06/114506.
• the dehydration reaction of glycerol is generally carried out on acidic solid catalysts.
• Suitable catalysts are materials used in a gaseous or liquid reaction medium, in a heterogeneous phase, which have a Hammett acidity, denoted H 0 of less than +2.
• H 0 Hammett acidity
• These catalysts may be chosen from natural or synthetic siliceous materials or acidic zeolites; inorganic carriers, such as oxides, coated with inorganic acids, mono, di, tri or polyacids; oxides or mixed oxides or heteropolyacids or salts of heteropolyacids.
• These catalysts can generally be constituted by a heteropoly acid salt in which protons of said heteropoly acid are exchanged with at least one cation selected from the elements belonging to Groups I to XVI of the Periodic Table of Elements, these heteropoly acid salts containing at least an element selected from the group consisting of W, Mo and V.
• mixed oxides mention may be made especially of those based on iron and phosphorus and those based on cesium, phosphorus and tungsten.
• the catalysts are chosen in particular from zeolites, Nafion® composites (based on sulphonic acid of fluorinated polymers), chlorinated aluminas, acids and salts of phosphotungstic and / or silicotungstic acids, and various solids of metal oxide type such as tantalum oxide Ta 2 Os, niobium oxide Nb 2 Os, alumina Al2O3, titanium oxide TiO 2 , zirconia ZrO 2 , tin oxide SnO 2 , silica SiO 2 or silico-aluminate SiO 2 -Al 2 Os, impregnated acidic functions such as BO3 borate, SO4 sulfate, WO3 tungstate, PO4 phosphate, SiO 2 silicate, or MOO3 molybdate, or a mixture of these compounds.
• metal oxide type such as tantalum oxide Ta 2 Os, niobium oxide Nb 2 Os, alumina Al2O3, titanium oxide TiO 2
• the foregoing catalysts may further comprise a promoter such as Au, Ag, Cu, Pt, Rh, Pd, Ru, Sm, Ce, Yt, Sc, La, Zn, Mg, Fe, Co, Ni, or montmorillonite gold.
• a promoter such as Au, Ag, Cu, Pt, Rh, Pd, Ru, Sm, Ce, Yt, Sc, La, Zn, Mg, Fe, Co, Ni, or montmorillonite gold.
• the preferred catalysts are zirconium phosphates, tungsten zirconias, zirconium silicates, titanium or tin oxides impregnated with tungstate or phosphotungstate, phosphated aluminas or silicas, heteropolyacids or salts. heteropolyacids, iron phosphates and iron phosphates comprising a promoter.
• the reaction medium leaving the dehydration reactor has a significant water content due to the glycerol charge (aqueous solution) and to the reaction itself.
• An additional step (1 ') of partial condensation of the water such as for example that described in the patent application WO 08/087315 in the name of the applicant, will eliminate a part, so as to bring this gas to a composition substantially identical to that of the ex-propylene process, to feed the second step of oxidation of acrolein to acrylic acid.
• substantially identical composition is meant in particular concentrations of acrolein, water and oxygen near.
• This condensation step (1 ') must be carried out with a cooling at a temperature which makes it possible, after removal of the condensed phase, to obtain a gas stream containing water and acrolein in a water / acrolein molar ratio of 1.5 / 1 to 7/1
• This partial condensation of the water makes it possible to avoid a degradation of the acrolein 2 rst stage oxidation catalyst in acrylic acid and to avoid at the subsequent stages the elimination of large quantities of water which are expensive to dispose of later and may lead to loss of acrylic acid.
• the oxidation reaction, step (2) is carried out in the presence of molecular oxygen or a mixture containing molecular oxygen, at a temperature ranging from 200 ° C. to 350 ° C., preferably 250 ° C. at 320 ° C., and at a pressure ranging from 1 to 5 bars in the presence of an oxidation catalyst.
• oxidation catalyst all types of catalysts well known to those skilled in the art are used for this reaction.
• Solids containing at least one element selected from the list Mo, V, W, Re, Cr, Mn, Fe, Co, Ni, Cu, Zn, Sn, Te, Sb, Bi, Pt, Pd, Ru, are generally used.
• Rh present in the metallic form or in the form of oxide, sulphate or phosphate.
• the formulations containing Mo and / or V and / or W and / or Cu and / or Sb and / or Fe are used as main constituents.
• the gaseous mixture resulting from step (2) consists, apart from acrylic acid: - light compounds that are incondensable under the conditions of temperature and pressure usually used: nitrogen, unconverted oxygen, carbon monoxide and carbon dioxide formed in small quantities by ultimate oxidation,
• condensable light compounds in particular water, generated by the dehydration reaction or as a diluent, unconverted acrolein, light aldehydes, such as formaldehyde and acetaldehyde, formic acid, acetic acid; and propionic acid
• the gaseous effluent from step (2) is subjected to a countercurrent absorption stage (3) by means of a hydrophobic heavy solvent which is accompanied by a cooling of the assembly.
• the gaseous effluent is introduced at the bottom of a column and the heavy solvent at the top of the column.
• the flow of solvent introduced at the top of the column is 3 to 6 times by mass that of the acrylic acid in the gaseous feed mixture.
• a heavy solvent solution having an acrylic acid content generally of between 15 and 25% by weight and containing, in addition, intermediate compounds having a boiling point between that of the heavy solvent and that of the solvent is collected at the bottom of the column. acrylic acid.
• intermediate compounds are constituted by the heavy products of the reaction: furfuraldehyde, benzaldehyde, maleic acid and anhydride, 2-butenoic acid, benzoic acid, phenol, protoanemonin and the stabilizing products introduced into the medium to inhibit the polymerization reactions.
• the light fraction, emerging at the top, consists of incondensable light compounds under the conditions of temperature and pressure usually used: nitrogen, unconverted oxygen, carbon monoxide and carbon dioxide formed in small quantities by ultimate oxidation, and light compounds.
• condensables in particular water, generated by the dehydration reaction or as a diluent, unconverted acrolein, light aldehydes, such as formaldehyde and acetaldehyde, formic acid, acetic acid.
• This hydrophobic heavy solvent extraction operation is well known and has even been described for the treatment of acrylic acid synthesized by oxidation of propylene;
• the following patents may be mentioned in this regard: French Patent No. 1,588,432, French Patent No. 2,146,386, German Patent No. 4,308,087, European Patent No. 0 706 986 and French Patent No. 2,756,280 which describe such solvents.
• French Patent No. 1,588,432 describes the use of acid esters. aliphatic or aromatic at high boiling point. They are most often constituted by binary mixtures capable of forming eutectics, such as, for example, diphenyl (DP) and diphenyl ether (DPO) which form a eutectic in a proportion of 26.5-76.5 (BF No. 2 146,386 and EP0706,986) or even ternary, DP-DPO-dimethylphthalate (DMP) (DE No. 4,308,087).
• DP diphenyl
• DPO diphenyl ether
• DMP ternary, DP-DPO-dimethylphthalate
• 2,756,280 recommends the use of aromatic solvents having a boiling point greater than 260 ° C. and comprising one or two aromatic rings substituted with at least one alkyl radical having from 1 to 4 atoms. carbon, or cycloalkyl, especially ditolyl ether alone or in the form of a mixture of its isomers or ditolyl ether mixture (DTE) and dimethylphthalate.
• aromatic solvents having a boiling point greater than 260 ° C. and comprising one or two aromatic rings substituted with at least one alkyl radical having from 1 to 4 atoms. carbon, or cycloalkyl, especially ditolyl ether alone or in the form of a mixture of its isomers or ditolyl ether mixture (DTE) and dimethylphthalate.
• DTE ditolyl ether mixture
• the process of the invention can be conducted with these various solvents.
• the preferred solvents are those described in this French patent No. 2,756,280 which, in addition to improving the separation of the impurities contained in the reaction mixture, reduce the phenomenon of entrainment of traces of solvent in the flow of compounds. incondensables recycled to the reaction section and allow efficient recovery of polymerization inhibitors.
• the liquid solution of acrylic acid in the heavy solvent is then sent to a topping zone, step (4), to eliminate in the head traces of water and light compounds. condensables that remain at the foot of the previous absorption zone. This heading zone is fed at the top by the foot flow of the absorption zone.
• the head stream enriched with light compounds is returned to the absorption zone, in order to eliminate these light compounds in its head flow.
• the liquid acrylic acid solution obtained at the bottom of this zone is then sent to the distillation zone for the separation of the heavy solvent and the acrylic acid (step 5); the heavy solvent is extracted at the bottom of said zone to be recycled, after treatment, in the first stage.
• the acrylic acid solution containing most of the intermediate compounds comes out of the said zone.
• This stream may optionally also contain some traces of solvent.
• the acrylic acid solution is then sent to a separation zone, on the one hand intermediate compounds and, on the other hand, purified acrylic acid (technical acrylic acid) (step 6).
• the intermediate compounds are extracted at the tail of the zone and the technical acrylic acid extracted at the top of said zone.
• the technical acrylic acid produced is then fed to the fractional crystallization zone.
• the different stages of separation by absorption or distillation require, due to the thermodynamic conditions used, to add polymerization inhibitors to the treated streams in order to avoid the formation of heavy compounds detrimental to the proper functioning of the assembly.
• the polymerization inhibitors generally used for the acrylic acid purification steps are phenolic products, such as hydroquinone or methyl ether of hydroquinone, phenothiazine derivatives, compounds of the family of thiocarbamates, such as copper n-butyl dithiocarbamate, amine derivatives, such as hydroxy-lamines, hydroxydiphenylamine, or phenylenediamine family, nitroxide derivatives of 4-hydroxy-2,2,6,6-tetramethyl-1 oxyl-piperidine (TEMPO), such as 4-hydroxy-TEMPO or 4-oxo-TEMPO, or metal salts, such as manganese acetate.
• TEMPO 4-hydroxy-2,2,6,6-tetramethyl-1 oxyl-piperidine
• metal salts such as manganese acetate.
• These polymerization inhibitors are generally heavy compounds, whose volatility is lower than that of acrylic acid, but may in some cases be lighter than the solvent. They are eliminated at the bottom of the columns when the inhibitors are heavier than the solvent, or are divided between the head flow and the foot flow for inhibitors that are lighter or close to the solvent. In most columns, their concentration in the vapor phase inside the distillation columns is low and insufficient to prevent the initiation of polymers. To prevent the appearance and accumulation of polymers, these additives are usually introduced into the liquid feeds to equipment, but also to the head and at different points of the columns and equipment, so as to ensure a constant and homogeneous reflux of rich solution in polymerization inhibitors on all parts of the equipment. In general, they are sent in solution in a liquid, for example in acrylic acid or in the solvent if the purification step concerns flows containing the solvent.
• the last step of the process of purification of bio-recycled acrylic acid is a separation by fractional crystallization thus associated with the previous purification steps.
• Fractional crystallization is a well-known separation technique. It can be implemented in various forms, dynamic crystallization, static crystallization or suspension crystallization. Mention may be made in this regard of French Patent 77 04510 of 17/02/1977 (BASF) and US Pat. No. 5,504,247 (Sulzer) and 5,831,124 (BASF) and 6,482,981 (Nippon Shokubai), some of which are directed to the purification of synthesized acrylic acid. by oxidation of propylene.
• the most widely used technique is fractional crystallization in falling film, dynamic crystallization, possibly associated with static crystallization in a molten medium.
• Falling film crystallization is generally carried out in a tubular exchanger, multitubular in practice, each tube being fed continuously (at the head), by:
• a coolant flow for example ethylene glycol-water or methanol-water, falling film, preferably along the outer wall of the tube, also recirculated throughout the crystallization within the tube and which will bring the cold or the heat necessary for the operation of the steps of each of the stages.
• é is a combination of successive stages, which each include 3 stages:
• Crystallization the temperature of the coolant is lowered according to a negative temperature gradient from a temperature slightly above the crystallization temperature of the acrylic acid in the medium, of the order of 14 ° C. form an increasingly thick layer on the surface of the tubes.
• a temperature slightly above the crystallization temperature of the acrylic acid in the medium of the order of 14 ° C. form an increasingly thick layer on the surface of the tubes.
• the temperature of the coolant is heated to a positive temperature gradient to melt out the impurities trapped as inclusions in the crystal layer of acrylic acid in formation, these are mainly located at the level of the the outermost layer that is in contact with a recirculated stream increasingly rich in impurities.
• the first molecules to be melted are eutectic mixtures of impurities and AA, impurities located in the crystal layer migrate to the outer layer that which was in contact with the recirculated flow. A small portion of this crystal layer is thus melted and transferred to a receptor, preferably the same receptor as that of mother liquors recovered during the crystallization step.
• melting the temperature of the coolant is rapidly increased beyond the melting point of AA (14 ° C) and should preferably remain below a maximum temperature beyond which there is a fear of (explosive) polymerization of medium: this maximum temperature is of the order of 35-40 0 C to remain safe to do melt the layer of purified AA crystals.
• the recovered purified liquid is placed in a second receiver.
• the purified liquid at the end of this first stage can again undergo a succession of the 3 steps described in a 2nd purification stage (purification phase).
• the mother liquors from this 2nd stage are purer than those of the previous stage and can thus be used in mixture with a new charge of AA to be purified in the stage 1.
• the same operation can be carried out in a third stage of purification, the mother liquors from this third stage can be recycled in the load of the 2nd floor, the pure product is recovered by melting the crystals.
• the mother liquors of the purification stage "n" can be recycled by mixing them with the feed stream of the "n-1" purification stage.
• the polymerization inhibitors contained in the mixtures to be purified are treated as impurities and are therefore eliminated in the mother liquors.
• an inhibitor which is compatible in nature and concentration is preferably added with the final use of the monomer. This addition will be implemented in particular during the last step of melting a stage fed by a stream free of polymerization inhibitor, such as for example the last purification stage "n" fed only with a purified stream of the floor "n-1".
• the mother liquors collected following the first purification stage can be treated in a "-1" stage according to the same three-stage process.
• the recovered crystallizate can be used as a supplement to the feedstock of the first stage.
• the mother liquors of the stage “-1” are then treated according to the same process for a new separation whose crystallizate will enter as the charge of the next higher stage and the mother-waters subjected again to the process in a lower stage " - 2 ".
• the stages "-1", “-2”, etc. constitute the concentration stages (the successive stages make it possible to concentrate the impurities in the flows of mother liquors).
• the mother liquors of the concentration stages "n" are treated according to the same 3-step process in the subsequent stage "n-1".
• concentration phase will allow impurities to be concentrated in a mother liquor stream that is increasingly rich in impurities. fractions of pure acrylic acid will be brought back to the initial stage. Thus, the acrylic acid entrained in the initial mother liquors can be recovered to improve the recovery yield and moreover obtain an "enriched" mixture of impurities.
• the successive concentration stages are characterized by mother liquor streams increasingly concentrated in impurities, as these stages are accumulated. In doing so, the crystallization temperature of these mixtures is becoming lower, which has the effect of increasing the energy cost of cooling. Furthermore, the time required to crystallize the same amount of acrylic acid is longer and longer, which has the effect of reducing the productivity of purification for the same crystallization surface. Therefore, the number of concentration steps will generally be preferably stopped before the total concentration of impurities in the mother liquors exceeds 50% by weight of the flux.
• “Technical” comprises at least 2 purification stages, preferably between 2 and 4 purification stages, and between 1 and 4 stages for the concentration of impurities.
• a last recovery stage in a static crystallizer.
• the mixture to be crystallized is placed in contact with a cooled wall.
• a cooled wall It may be for example an exchanger consisting of metal plates circulated by a heat transfer fluid, immersed in a vessel containing the mother liquors of crystallization of the previous stages.
• the AA forms a crystal layer on the wall of the plates, then the mother liquors are removed and the crystallized layer is melted for further processing in a falling film dynamic crystallization upper stage.
• FIGS. 1 to 4 schematically illustrate the different embodiments.
• the symbols of the main heat exchangers have been symbolized on the diagrams by a down arrow for the cooling stages, a rising arrow for the warming stages Figure 1 :
• the reaction gas stream (1) is introduced at the bottom of the absorption column C1, which countercurrently receives a heavy solvent or a mixture of hydrophobic heavy solvents.
• the liquid stream (2) still contains water and light (especially acetic acid). It is sent to a distillation column C2 which makes it possible to recover the water and the light ones (acetic acid) at the top, in the stream (3) which is recycled towards the column C1.
• the gas stream (14) contains all incondensable compounds (nitrogen, oxygen, CO, CO 2 ) and light compounds (acetaldehyde, acrolein, acetic acid, water, ). This stream (14) can be partially recycled to the reaction (15) and partially or completely purged (16).
• the liquid mixture contains AA (15-25%) in solution in the solvent, and the intermediate heavy compounds (with a boiling point between that of the AA and that of the solvent, as maleic anhydride, furfural, benzaldehyde, protoanemonin, 2-butenoic acid, etc.) and any compounds present which would be heavier than the solvent.
• the flow (9) is recycled at the top of the absorption column C 1, possibly after purging (10 and 11) in all or part of the stream (9) of the compounds heavier than the solvent in an evaporator, the flow of evaporator containing the recoverable solvent (12).
• the stream (17) is then sent to a distillation column C4 which separates the technical grade AA at the top (6) and the "heavy" at the bottom (5), composed of the solvent and the intermediates.
• This stream (5) can then be purified in an additional column (not shown in the diagram) in order to eliminate the intermediate heavy compounds at the top and recover the foot solvent and inhibitors, the latter foot stream can then be recycled to upstream of the process.
• column C2 does not remove all of this impurity.
• the flow of technical AA (6) still contains acetic acid, as well as propionic acid and 2-butenoic acid.
• This stream (6) is purified by fractional crystallization which makes it possible to eliminate both acetic acid, propionic acid and 2-butenoic acid.
• liquid phase resulting from step (3) is subjected to
• step 5 a distillation top with separation at the top of the water and residual light (step 4), the bottoms fraction being sent to a step 5,
• the stream (4) feeds a column C3 comprising 3 sections, from bottom to top, Sl, S2 and S3.
• This single column fulfills the functions of columns C3 and C4 of FIG. 1.
• Feeding by stream 4 takes place at the tail of section S1.
• a stream (5) rich in intermediate heavy impurities and containing a little solvent and optionally stabilizers is recovered.
• This stream may be treated as described above to recover the solvent and the stabilizer for recycling upstream of the process.
• the tail of S3, the solvent 9 and the heavy compounds which are recycled to the absorption column after preliminary treatment via 10, 11, 12 and 13 are recovered in stream 9.
• liquid phase resulting from step (3) is subjected to
• step 4 the bottoms fraction being addressed to a step 5
• liquid phase resulting from step (3) is subjected to
• step 4 a fractionation by distillation in an area comprising two sections with separation at the top of the water and residual light, at the tail of the heavy solvent and by side withdrawal, at the border of the two sections, of the acrylic acid (step 4), - A purification of the acrylic acid from the side withdrawal of step (4) by fractional crystallization.
• This stream (6) is purified by crystallization.
• the flow (4) at the bottom of the column C2 is sent to a column C3 to remove at the top (5) a stream containing the bulk of the intermediate heavy compounds, with a little solvent.
• This stream (5) can then be treated as described above to recover the solvent and optionally stabilizers which will be recycled upstream of the process.
• the invention also relates to the use of the bio-resourced acrylic acid obtained according to the process of the invention for the manufacture of homopolymers and copolymers produced by polymerization of acrylic acid and optionally other unsaturated monomers, by example the manufacture of superabsorbent polymers obtained by polymerization of said partially neutralized acid, or the polymerization of said acid followed by a partial neutralization of the polyacrylic acid obtained.
• the invention also relates to polymers and copolymers obtained by polymerization of bio-resourced acrylic acid and possibly other bio-recycled monomers or from fossil raw materials.
• the invention also relates to the superabsorbents obtained by polymerization of bio-resourced acrylic acid.
• the invention also relates to the use of bio-resourced acrylic acid for the manufacture of polymers or copolymers by polymerization of derivatives of said acid in ester or amide form. It also relates to polymers or copolymers obtained by polymerization of the derivatives in ester or amide form of bio-resourced acrylic acid.
• the preliminary step is to purify the crude glycerol obtained from vegetable oil, removing the salts.
• the crude glycerol solution consists of 89.7% glycerol, 3.9% water and 5.1% sodium chloride.
• This stream (6,400 g) is continuously fed to a stirred reactor of 2 liters heated by an external electric reactor heater.
• the glycerol and water vapors are condensed in a refrigerant and recovered in a receiver.
• This purification operation is carried out under a pressure of 670 Pa (5 mm Hg). 5 710 g of a solution of glycerol free of sodium chloride are obtained.
• step (1) of the process the dehydration reaction of glycerol to acrolein and the condensation (1 ') of part of the water is carried out.
• the dehydration reaction is carried out in the gas phase in a fixed bed reactor in the presence of a solid catalyst consisting of a ZrO 2 -WO 5 tungsten zirconia at a temperature of 320 ° C. under atmospheric pressure.
• a mixture of glycerol (20% by mass) and water (80% by mass) is sent into a vaporizer, in the presence of air, in an O 2 / glycerol molar ratio of 0.6 / 1.
• the gaseous medium leaving the vaporizer at 290 0 C is introduced in the reactor, consisting of a 30 mm diameter tube loaded with 390 ml of catalyst, immersed in a salt bath (eutectic mixture KNO3, NaNO 3 , NaNO 2 ) maintained at a temperature of 320 ° C.
• a salt bath eutectic mixture KNO3, NaNO 3 , NaNO 2
• the gaseous reaction mixture is sent at the bottom of a condensation column.
• This column consists of a lower section filled with raschig rings, surmounted by a condenser circulated by a cold heat transfer fluid.
• the cooling temperature in the exchangers is adapted so as to obtain at the top of the column a vapor temperature of 72 ° C. under atmospheric pressure. Under these conditions, the loss of acrolein at the bottom of the condensation column is less than 5%.
• the gaseous mixture is introduced, after addition of air (molar ratio O 2 / acrolein of 0.8 / 1) and nitrogen in the amount necessary to obtain an acrolein concentration of 6. , 5 mol%, for feeding the acrolein oxidation reactor with acrylic acid.
• This oxidation reactor consists of a 30 mm diameter tube charged with 480 ml of a commercial acrolein oxidation catalyst made of acrylic acid based on mixed oxides of aluminum, molybdenum, silicon, vanadium and copper immersed in a bath of salt identical to that described above, maintained at a temperature of 250 ° C. Before introduction on the catalyst bed, the gaseous mixture is preheated in a tube also immersed in the salt bath.
• the gaseous mixture (1) is introduced at the bottom of an absorption column C1, step (3) operating at atmospheric pressure.
• This column is filled with ProPak stainless steel bulk packing.
• the column is equipped with a condensing section, at the top of which is recycled a portion of the condensed mixture recovered at the bottom of the column, after cooling to 70 0 C in a heat exchanger external.
• a stream (14) consisting of DTE (ditolyl ether) is fed at a temperature of 54 ° C., with a mass ratio of solvent / acrylic acid contained in the reaction gas of 4/1, in which it has previously been dissolved 0.5% EMHQ as a polymerization inhibitor.
• the temperature of the vapors at the top of the column is 52 ° C., that of the acrylic acid solution obtained at the bottom of the column is 84 ° C.
• the product (2) obtained at the bottom is cooled to a temperature of 35 ° C, and is sent using a pump at the head of a column C2 equipped with 15 perforated trays spillways.
• the distillation is carried out in this column at a pressure of 187 hPa.
• the temperature measured at the bottom of the column is 113 ° C. and the temperature at the top of the column is 88 ° C. All condensed vapors at the top (3) are returned to the external cooling loop of column Cl.
• the flow (4) extracted at the bottom of this column is crude acrylic acid, which has a title of 20.2% of acrylic acid.
• concentrations of impurities in the flow are 0.72% acetic acid, 0.81% propionic acid, 0.01% furfural, 0.02% protoanemonin, , 03% benzaldehyde, 0.04% 2-butenoic acid, 0.41% maleic anhydride.
• the flow of crude acrylic acid obtained in the preceding step is fed to a column C3 operating under a pressure of 117 hPa equipped with 4 perforated trays each provided with a weir, fed between the 2nd and 3rd tray.
• the technical acrylic acid obtained at the top of the column is titled 98% AA.
• the impurities present in this flow are acetic acid (0.68%), propionic acid (0.76%), furfural (0.005%), protoanemonin (0.009%), benzaldehyde (0.012%), 2-butenoic acid (0.016%), maleic anhydride (0.12%), water (0.21%) ) and the DTE (0.005%).
• the technical grade acrylic acid stream obtained in Example 1 is subjected to a series of fractional crystallization purification and concentration stages as described herein.
• the assembly used is a drop-flow crystallizer consisting of a vertical stainless steel tube filled with heat transfer fluid (ethylene glycol-water mixture) circulating in a closed circuit, via a pump, through an external heat exchanger programmable in a temperature ramp (bath cryostat Lauda).
• This tube is fed at the top in the form of a liquid film flowing uniformly on its outer wall.
• Crystallization the coolant is rapidly cooled so as to lower the temperature of the falling film of acrylic acid to the crystallization temperature of the acrylic acid in the mixture, determined beforehand from a sample of the mixture to be purified; then a negative temperature gradient is imposed on the coolant, 0.1 to 0.5 ° C / min.
• the volume of crystallized acrylic acid measured by difference by evaluating the liquid level in the collector at the bottom of the crystallizer, reaches 70% of the starting mixture, the recirculation of the falling film of the mixture to be purified is stopped, and the tube is drained.
• the liquid mixture of mother liquors thus obtained is separated and stored in a recipe.
• the melt purified product in the last stage of the first purification stage is sent to the second purification stage, where it will be subjected to a new series of 3 purification steps under the same operating conditions.
• the mother liquors of the second purification stage are then mixed with a new feed of the technical AA feed stream in stage 1. This process is repeated thus until obtaining the desired quality in the purified melt product.
• the last crystallization stage is realized static mode.
• the stream to be purified is placed in a double-walled stainless steel vessel circulated by a cold fluid maintained at the crystallization temperature of the medium, previously determined by a crystallization temperature measurement.
• a vertical stainless steel tube filled with heat transfer fluid ethylene glycol-water mixture circulating in a closed circuit, via a pump, is immersed through an external heat exchanger programmable in a temperature ramp.
• a first step the temperature of the coolant in the tube is rapidly lowered to the temperature of crystallization of the medium, then a negative temperature gradient of 0.1 to 0.5 ° C./min.
• the crystallized volume reaches approximately 50% of the starting material, the mother liquors are removed, then a bleeding step is carried out and finally the melting step, as in the upper stages of crystallization in dynamic mode.
• the concentration of acrylic acid in the residual mother liquors of the final concentration stage is 71%.
• the recovery yield of AA in this purification step is 97.2%.
• the AA concentration in the ultimate mother liquors is 54.3% and the overall purification efficiency is 99.3%.
• the residue has the following composition by weight: AA: 54.3%; water: 7.3%; maleic anhydride: 8.9%; protoanemonin: 1%; benzaldehyde: 2%; acetic acid: 4.3%; propionic acid: 16.7%; acrolein: 1.6%; furfural: 0.8%; 2-butenoic acid: 2%.
• the acrylic acid produced according to the invention is a bio-resourced acid made from non-fossil natural raw materials.
• non-fossil natural carbonaceous raw materials can be detected by the carbon atoms used in the composition of the final product.
• materials composed of renewable raw materials contain the 14 C radioactive isotope. All carbon samples taken from living organisms (animals or plants) are in fact a mixture of 3 isotopes: 12 C (representing 98.892%), 13 C ( ⁇ 1.108%) and 14 C (traces: 1, 2.10 "10 %) The 14 C / 12 C ratio of the living tissues is identical to that of the CO 2 of the atmosphere .
• the constancy of the 14 C / 12 C ratio in a living organism is related to its metabolism with continuous exchange with the atmosphere.
• the decay constant of 14 C is such that the 14 C content is practically constant from the harvesting of plant raw materials to the production of the final product.
• the bio-resourced acrylic acid obtained by the process of the invention has a mass content of 14 C such that the ratio 14 C / 12 C is greater than 0.8.10 "12 and preferably greater than 1.10 12 .
• Measurement of the 14 C content of the materials is precisely described in ASTM D6866 (including D6866-06) and ASTM D7026 (including 7026-04).

Landscapes

• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Engineering & Computer Science (AREA)
• Oil, Petroleum & Natural Gas (AREA)
• Crystallography & Structural Chemistry (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Applications Claiming Priority (2)

Publications (1)

Family

ID=41510613

Family Applications (1)

Country Status (10)

Families Citing this family (6)

Family Cites Families (22)

• 2009
  • 2009-07-22 FR FR0955112A patent/FR2948366B1/fr not_active Expired - Fee Related
• 2010
  • 2010-06-29 CN CN2010800420258A patent/CN102482189A/zh active Pending
  • 2010-06-29 EP EP10745373A patent/EP2456746A1/fr not_active Withdrawn
  • 2010-06-29 BR BR112012001326A patent/BR112012001326A2/pt not_active IP Right Cessation
  • 2010-06-29 SG SG2012004743A patent/SG177732A1/en unknown
  • 2010-06-29 KR KR1020127003316A patent/KR20120038479A/ko not_active Application Discontinuation
  • 2010-06-29 US US13/386,096 patent/US20120190890A1/en not_active Abandoned
  • 2010-06-29 JP JP2012521074A patent/JP2012533610A/ja not_active Abandoned
  • 2010-06-29 WO PCT/FR2010/051363 patent/WO2011010036A1/fr active Application Filing
• 2012
  • 2012-01-20 IN IN601DEN2012 patent/IN2012DN00601A/en unknown

Non-Patent Citations (1)

Also Published As

Similar Documents

Legal Events