Organic compounds -- part of the class 532-570 series – Organic compounds – Carboxylic acids and salts thereof
Reexamination Certificate
2001-06-12
2003-05-13
Raymond, Richard L. (Department: 1624)
Organic compounds -- part of the class 532-570 series
Organic compounds
Carboxylic acids and salts thereof
Reexamination Certificate
active
06563001
ABSTRACT:
The present invention relates to the processing of the reaction mixture from the direct oxidation of hydrocarbon into carboxylic acid, more particularly the reaction mixture from the oxidation reaction of cyclohexane to adipic acid, and to the separation of the various constituents of the said mixture and to the purification of the carboxylic acid produced in the oxidation reaction.
The direct oxidation of cyclohexane to adipic acid is a process which has been under investigation for a long time, in particular on account of the obvious advantages there would be in converting cyclohexane to adipic acid, in a single step and without using an oxidizing agent such as nitric acid, since this compound generates nitrogen oxides which then need to be processed in order to avoid any pollution.
Patent WO-A-94/07834 describes the oxidation of cyclic hydrocarbons into the corresponding diacids, in a liquid phase comprising a solvent, using a gas containing oxygen and in the presence of an oxidation catalyst such as a cobalt compound, the said solvent comprising an organic acid containing only primary or secondary hydrogen atoms. That patent more particularly develops the phases for processing the final reaction mixture. This processing consists in separating out the diacid formed, cooling the mixture to bring about precipitation of the said diacid, separating the diacid, by filtration, from two liquid phases, a nonpolar phase which is recycled and a polar phase which is also at least partially recycled after an optional hydrolysis, and a separation of a further amount of diacid.
That patent proposes a solution for the one-step oxidation of cyclohexane into adipic acid with industrially acceptable selectivity, but it does not give an industrially acceptable solution to the processing of the reaction mixture from the oxidation, taking into account separation of the various reaction products and side products, the unconverted materials and the catalyst.
In addition, it is found, in practice, that such a concise processing process does not give an adipic acid of the purity required for a great many applications of this highly important starting material.
Specifically, whether it is for the production of polyamide 6-6 or for other applications such as the production of certain polyurethanes, the purity of the adipic acid used must be extremely high, in particular as regards the contents of organic side products which can introduce undesirable colorations.
Patent WO-A-96/03365 describes a more complete process for processing the reaction mixture from the direct oxidation of cyclohexane into adipic acid, as well as the recycling of the catalyst. However, the Applicant has observed that the presence of oxidation intermediates and side products, in particular such as cyclohexanone, cyclohexanol, cyclohexyl esters, hydroxycarboxylic acids and lactones, is liable to interfere with the separation and purification of the adipic acid. The present invention proposes a process which avoids this type of drawback.
More specifically, the invention consists of an improved process for processing the reaction mixture from the direct oxidation of hydrocarbon into carboxylic acid, using molecular oxygen or a gas containing it, in the liquid phase, in a solvent and in the presence of a catalyst dissolved in the reaction medium, characterized in that the said process comprises:
when the composition of the reaction mixture allows it, a decantation into two liquid phases: a nonpolar upper phase essentially containing the unconverted hydrocarbon, and a polar lower phase essentially comprising the solvent, the acids formed, the catalyst and some of the other reaction products and of the unconverted hydrocarbon;
a distillation of the said lower phase or, where appropriate, of all of the reaction mixture, thus separating, on the one hand, a distillate comprising all or at least most of the unconverted hydrocarbon and, on the other hand, the distillation residue comprising the acids formed, the catalyst, the heavy compounds, at least some of the solvent and, if any, the reaction intermediates and side products;
a purification treatment by oxidation, using molecular oxygen or a gas containing it or using oxygen donors, of the distillation residue obtained above,
a distillation of the reaction solvent and the reaction intermediates and side products which may still remain in the mixture,
a crystallization of the carboxylic acid produced in the reaction;
a recrystallization from water of the carboxylic acid produced in the reaction.
The decantation into two phases of the reaction mixture subjected to the process of the invention depends essentially on the solvent used and the amount of hydrocarbon converted.
The hydrocarbons used as starting materials in the process of the invention are, more particularly, alkanes, cycloalkanes and alkylaromatic hydrocarbons containing from 3 to 20 carbon atoms.
Among these hydrocarbons, cycloalkanes, in particular those which have a ring containing from 5 to 12 carbon atoms, are without doubt the most important, since their oxidation leads to dicarboxylic acids.
The most advantageous hydrocarbon is cyclohexane, oxidation of which leads to adipic acid, one of the base compounds of polyamide 6-6.
For convenience, hereinbelow the invention will be described very generally for the processing of the reaction mixtures from the oxidation of cyclohexane into adipic acid, but the process can also be applied to mixtures obtained from other hydrocarbons, and more particularly from other cycloalkanes.
The cyclohexane phase obtained in the optional decantation step is usually reintroduced into a cyclohexane oxidation operation.
The solvent used in the oxidation of the hydrocarbon, preferably cyclohexane, is an at least partial solvent for the carboxylic acid whose preparation is intended. This solvent can be very varied in nature, provided that it is not substantially oxidizable under the reaction conditions. It can be chosen in particular from polar protic solvents and polar aprotic solvents. Polar protic solvents which may be mentioned, for example, are carboxylic acids which contain only primary or secondary hydrogen atoms, in particular aliphatic acids containing from 1 to 9 carbon atoms, perfluoroalkylcarboxylic acids such as trifluoroacetic acid, water and alcohols. Polar aprotic solvents which may be mentioned, for example, are lower alkyl (=alkyl radical containing from 1 to 4 carbon atoms) esters of carboxylic acids, in particular of aliphatic carboxylic acids containing from 1 to 9 carbon atoms or of perfluoroalkylcarboxylic acids, tetramethylenesulphone (or sulpholane), and aliphatic nitrites 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 or copper, or a mixture of manganese with one or more other metals such as chromium, iron, zirconium, hafnium or copper. Among the cobalt-based mixtures, catalysts comprising either cobalt and chromium, cobalt, chromium and zirconium, cobalt and iron, 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 processed by the process of the invention contains, as a guide, on a weight for weight basis, from 1% to 99% of unconverted hydrocarbon, from 1% to 40% of carboxylic acids formed, from 0.1% to 10% of water, from 0.001% to 5% of the metal(s) contained in the catalyst and from 0.1% to 10% of other products of the oxidation reaction, the remainder consisting of the solvent.
The step for distillation of the lower phase or, where appropriate, of the reaction mixture, is carried out such that most, and as far as is possible all, of the unconverted cyclohexane which may still be present in this lower phase is separated from the ad
Costantini Michel
Fache Eric
Marin Gilbert
Raymond Richard L.
Rhodia Fiber & Resin Intermediates
Tucker Zachary C.
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