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
  • 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
  • C07C51/43—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
  • C07C51/487—Separation; Purification; Stabilisation; Use of additives by treatment giving rise to chemical modification

Definitions

• the present invention relates to the treatment of the reaction mixture resulting from the direct oxidation of hydrocarbon to carboxylic acid, more particularly to the reaction mixture resulting from the reaction of oxidation of cyclohexane to adipic acid, and the separation of the various constituents of said mixture and the purification of the carboxylic acid produced by the oxidation reaction.
• the direct oxidation of cyclohexane to adipic acid is a process which has been worked on for a long time, in particular because of the obvious advantages that there would be to convert cyclohexane to adipic acid, in a single step and without using an oxidizing agent such as than nitric acid, this compound generating nitrogen oxides which must then be treated to avoid any pollution.
• WO-A-94/07834 describes the oxidation of cyclic hydrocarbons to the corresponding diacids, in the liquid phase comprising a solvent, using an oxygen-containing gas and in the presence of a catalyst. oxidation such as a cobalt compound, said solvent comprising an organic acid having only primary or secondary hydrogen atoms.
• This patent more particularly develops the treatment phases of the final reaction mixture. This treatment consists in separating the diacid formed, by cooling the mixture to cause the precipitation of said diacid, in separating by filtration the diacid from two liquid phases, a non-polar which is recycled, a polar which is also at least partially recycled after a possible hydrolysis and separation of an additional quantity of diacid.
• This patent proposes a solution for oxidizing cyclohexane to adipic acid in one step with an industrially acceptable selectivity, but it does not provide a solution applicable industrially to the treatment of the reaction mixture resulting from oxidation, taking into account the separation of the different products and reaction byproducts, unprocessed products and catalyst.
• the purity of the adipic acid used must be extremely high, in particular for the contents of organic products which can cause undesirable coloring.
• WO-A-96/03365 describes a more complete process for treating the reaction mixture resulting from the direct oxidation of cyclohexane to adipic acid, as well as the recycling of the catalyst.
• the Applicant has observed that the presence of oxidation intermediates and by-products, such as in particular cyclohexanone, cyclohexanol, cyclohexyl esters, hydroxycarboxylic acids and lactones, is capable of disturbing the separation and the purification. adipic acid.
• the present invention provides a method which avoids this type of drawback.
• an upper non-polar phase essentially containing the unconverted hydrocarbon
• a lower polar phase essentially comprising the solvent, the acids formed, the catalyst and part of the other reaction products and unprocessed hydrocarbon
• the decantation into two phases of the reaction mixture subjected to the process of the invention essentially depends on the solvent used and the amount of hydrocarbon transformed.
• the hydrocarbons which are used as starting substrates in the process of the invention are more particularly alkanes, cycloalkanes and alkyl-aromatic hydrocarbons, having from 3 to 20 carbon atoms.
• cycloalkanes in particular those which have a ring having 5 to 12 carbon atoms, are certainly the most important, because their oxidation leads to dicarboxylic acids.
• the most interesting hydrocarbon is cyclohexane, the oxidation of which leads to adipic acid, one of the basic compounds of polyamide 6-6.
• the cyclohexane phase obtained in the possible decantation step is most often reintroduced in a cyclohexane oxidation operation.
• the solvent used in the oxidation of the hydrocarbon is an at least partial solvent for the carboxylic acid whose preparation is targeted.
• This solvent can be very varied in nature insofar as it is not substantially oxidizable under the reaction conditions. It can in particular be chosen from polar protic solvents and polar aprotic solvents.
• polar protic solvents mention may, for example, be made of carboxylic acids having only primary or secondary hydrogen atoms, in particular aliphatic acids having from 1 to 9 carbon atoms, perfluoroalkylcarboxylic acids such as trifluoroacetic acid, , alcohols.
• lower alkyl esters alkyl radical having from 1 to 4 carbon atoms
• carboxylic acids in particular aliphatic carboxylic acids having from 1 to 9 carbon atoms or perfluoroalkylcarboxylic acids, tetramethylenesulfone (or sulfolane), aliphatic nitriles such as acetonitrile.
• Acetic acid is generally preferred, in particular when the substrate to be oxidized is cyclohexane.
• the catalyst preferably contains cobalt, manganese, a mixture of cobalt with one or more other metals such as manganese, chromium, iron, zirconium, hafnium, copper, a mixture of manganese with one or more others metals such as chromium, iron, zirconium, hafnium, copper.
• the catalysts comprising either cobalt and chromium, or cobalt, chromium and zirconium, or cobalt and iron, or cobalt and manganese, or cobalt and zirconium and / or hafnium are more particularly suitable.
• This catalyst is used for the oxidation of cyclohexane, in the form of compounds of these metals which are soluble in the reaction medium.
• the reaction mixture to be treated by the process of the invention contains, for information by weight by weight, from 1% to 99% of unprocessed hydrocarbon, from 1% to
• heavy or heavy compounds are meant the compounds formed having a boiling point higher than that of the hydrocarbon and of the reaction intermediates indicated above and which are not the dicarboxylic acids, adipic acid, glutaric acid. and succinic acid, formed by the oxidation reaction.
• This step makes it possible, during the oxidation step of the reaction intermediates, such as cyclohexanol, cyclohexanone, cyclohexyl carboxylates, hydroxycarboxylic acids (hydroxycaproic acid), lactones (essentially butyrolactone, valerolactone) to avoid oxidizing a new quantity. cyclohexane and therefore re-form intermediates and reaction by-products.
• the distillation step is generally carried out at a temperature of 25 ° C to 250 ° C and under an absolute pressure between 10 Pa and atmospheric pressure. Preferably the temperature of the mixture during distillation will be maintained between 70 ° C and 150 ° C.
• an inert entrainer can be used in the distillation, which can be an inert gas such as nitrogen or steam.
• the distillate obtained in the distillation operation essentially comprises the unprocessed cyclohexane, optionally water and reaction intermediates such as cyclohexanol and cyclohexanone.
• the cyclohexane and the intermediates are recycled in a new oxidation reaction of the cyclohexane, after at least partial elimination of the water by any known means, in particular by azeotropic distillation.
• the oxidation of the distillation bottoms (secondary oxidation) is catalyzed by the catalyst used in the main oxidation reaction of the hydrocarbon. Taking into account the quantities of reaction intermediates, small compared to the quantity of hydrocarbon used in the main reaction, the catalyst is found in relatively large quantity, compared to the compounds to be oxidized.
• Secondary oxidation can be carried out with pure oxygen, with air or with other gaseous mixtures containing oxygen, such as, for example, air enriched or depleted in oxygen. It can also be carried out with oxygen donors, such as for example hydrogen peroxide or hydroperoxides organic like tert-butyl hydroperoxide, cyclohexyl hydroperoxide, cumyl hydroperoxide.
• oxygen donors such as for example hydrogen peroxide or hydroperoxides organic like tert-butyl hydroperoxide, cyclohexyl hydroperoxide, cumyl hydroperoxide.
• the pressure used for this oxidation can vary within wide limits. Generally the absolute pressure is between 1 bar (0.1 MPa) and 100 bar (10 MPa) and preferably between 5 bar (0.5 MPa) and 50 bar (5 MPa).
• the temperature can also vary widely, for example from 25 ° C to 250 ° C.
• the oxidation is carried out at a temperature of 40 ° C to 150 ° C.
• the solvent and the other liquid compounds which may be still present are distilled, so as to obtain a mixture essentially containing the dicarboxylic acids formed and the catalyst.
• Adipic acid is then crystallized from water or from an organic solvent which at least partially solubilizes adipic acid when hot.
• This organic solvent can be chosen in particular from ketones, carboxylic acids, esters of carboxylic acids, alcohols, aliphatic nitriles.
• the adipic acid obtained by this crystallization is then recrystallized from water, in order to achieve the purity necessary for the main applications where it is used.
• the recrystallization can be preceded by a black treatment further improving the desired purity.
• the process of the invention makes it possible to obtain pure adipic acid under conditions which do not require an additional catalyst to transform the intermediate compounds and / or the heavy compounds formed in the reaction oxidation of the hydrocarbon.
• the present process also does not require the consumption of an additional reagent such as nitric acid and therefore avoids the corresponding industrial investment.
• the temperature in the autoclave is maintained at around 105 ° C.
• the continuous injection of the liquid phase is started: injection of an acetic acid solution containing 1.1% by weight of acetate of cobalt tetrahydrate and 1.44% by weight of cyclohexanone at a flow rate of 4.6 ml / min (stabilized regime) and injection of cyclohexane at a flow rate of 5 ml / min (stabilized regime).
• the liquid product is continuously stored in a 7 liter decanter at 70 ° C.
• the content of the decanter is a two-phase mixture.
• the upper phase essentially cyclohexane, which contains little product and cobalt, is separated.
• the lower acetic phase (2668 g) contains most of the oxidation and cobalt products.
• the acetic phase is subjected to a first distillation under the following conditions: - pressure: 60 kPa - Temperature: 120 ° C. The purpose of this distillation is to remove all of the cyclohexane.
• the distillate has a mass of 1773 g.
• Half of distillation bottom 1 (447.5 g) is subjected to a second, more advanced distillation intended to remove all the volatile organic compounds which it contains by means of an injection of water vapor at 150 ° C. under pressure 10 kPa.
• the distillate has a mass of 222.5 g.
• the second half of distillation bottom 1 (447.5 g) of Example 1 is diluted in 400 ml of additional acetic acid and subjected to a further oxidation in air.
• the 847.5 g of the above solution are introduced into the 1.5 I titanium autoclave, inert with nitrogen. After closing the autoclave, the nitrogen pressure is brought to 20 bar (2 MPa), stirring (1000 rpm) started and the temperature brought to 105 ° C in 20 minutes. The nitrogen is then replaced by 20 bar of air. The inlet gas flow rate is adjusted to 250 liters per hour. After 3 h, the autoclave is cooled to 70 ° C, depressurized. The oxidized mass is recovered and subjected to type 2 distillation (10 kPa, 150 ° C, steam injection).
• the cobalt catalyst is found in the water of crystallization and washing.
• the batches of adipic acid (A) and (B) are subjected to a heating test.
• This test consists of heating 50 g of each batch at 215 ° C for 205 min, then placing each of them in 415 ml of a 5% aqueous ammonia solution.
• the purified adipic acid (B) according to the present invention contains fewer impurities capable of coloring on heating.

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• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
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• Oil, Petroleum & Natural Gas (AREA)
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• Chemical Kinetics & Catalysis (AREA)
• General Chemical & Material Sciences (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
• Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

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• 1998
  • 1998-09-14 FR FR9811591A patent/FR2784099B1/fr not_active Expired - Fee Related
• 1999
  • 1999-09-13 TW TW088115739A patent/TW522147B/zh not_active IP Right Cessation
  • 1999-09-14 SK SK351-2001A patent/SK3512001A3/sk unknown
  • 1999-09-14 AR ARP990104596A patent/AR020437A1/es unknown
  • 1999-09-14 BR BR9913719-4A patent/BR9913719A/pt not_active IP Right Cessation
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  • 1999-09-14 WO PCT/FR1999/002182 patent/WO2000015598A1/fr not_active Application Discontinuation
  • 1999-09-14 CN CN99812590A patent/CN1348435A/zh active Pending
  • 1999-09-14 CA CA002343013A patent/CA2343013A1/fr not_active Abandoned
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  • 1999-09-14 US US09/787,116 patent/US6563001B1/en not_active Expired - Fee Related
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