Organic compounds -- part of the class 532-570 series – Organic compounds – Carboxylic acids and salts thereof
Reexamination Certificate
2003-01-03
2004-09-21
Richter, Johann (Department: 1621)
Organic compounds -- part of the class 532-570 series
Organic compounds
Carboxylic acids and salts thereof
C562S598000
Reexamination Certificate
active
06794540
ABSTRACT:
BACKGROUND OF THE INVENTION
Various processes are known for the preparation of sorbic acid.
A particularly commercial process starts from the polymeric polyester reaction product prepared by reacting crotonaldehyde with ketene in an inert solvent in the presence of a fatty acid salt of a divalent and/or trivalent metal of group IIB to VIII of the periodic table as catalyst. The sorbic acid is obtained therefrom by alkaline hydrolysis and reaction with a strong acid (DE-AS 1 042 573).
However, sorbic acid can be obtained in various ways from this polyester.
DE-AS 1 059 899 describes the cleavage of the polyester to sorbic acid in the presence of an inert solvent which boils above 150° C. This solvent acts simultaneously as solvent for the polyester and as entrainer for the distillation of the sorbic acid formed therefrom. Alkali metal hydroxides or alkaline salts of organic acids are added as catalyst to the polyester or the mixture containing the latter.
An industrially important process for preparing sorbic acid consists of carrying out the cleavage of the polyester in the presence of an amine which boils above 150° C. as catalyst at temperatures of from 160 to 220° C. with simultaneous distillation out of the sorbic acid and of the solvent (DE-AS 1 282 645). The solvents used in this case are the solvents mentioned in DE-AS 1 059 899, in particular the aliphatic carboxylic acids having an appropriate boiling point mentioned therein.
When this process is carried out industrially, the polyester cleavage is carried out in a continuously operated distillation apparatus. The sorbic acid polyester dissolved in the solvent is metered into the distillation vessel where the amine-catalysed cleavage of the sorbic acid polyester to sorbic acid takes place. The sorbic acid which is formed is distilled out together with the solvent through a rectification column with reflux. The reflux is thus the distillate, i.e. a mixture of solvent and sorbic acid. The rectification is necessary in order to prevent the amine passing into the distillate and in order to achieve an appropriate purity of the sorbic acid. The sorbic acid is then crystallized out of the distillate and separated from the solvent. The solvent is recycled.
In the thermal cleavage of sorbic acid polyester there is formation in the distillation vessel not only of sorbic acid but also of polymers which must be continuously discharged. However, amine catalyst is also discharged thereby. On the one hand, this means a not inconsiderable loss of yield due to polymer formation and, on the other hand, amine catalyst must be continuously fed in to compensate for the losses due to the discharge.
The object therefore was to develop a process in which the polymer formation during the cleavage of sorbic acid polyester is reduced and thus both the yield of sorbic acid is increased and the consumption of amine is reduced.
BRIEF DESCRIPTION OF THE INVENTION
It has now been found, surprisingly, that polymer formation during the distillation can be markedly reduced with only the solvent, and not the distillate as in the prior art, is used as reflux. The result is a very pure sorbic acid with, at the same time, an increased yield and a reduction in the necessary input of amine as catalyst.
Flow diagram 1 shows diagrammatically the distillation process used in the prior art for the polyester cleavage, in which distillate taken off at the top of the column (mixture of sorbic acid and solvent) is fed as reflux into the rectification column.
Flow diagram 2 shows diagrammatically the distillation process according to the present invention, in which the solvent which has distilled out is, after removal of the sorbic acid, fed as reflux into the rectification column.
DETAILED DESCRIPTION OF THE INVENTION
The present invention thus relates to a process for the preparation of sorbic acid by thermal cleavage of the polyester prepared from crotonaldehyde and ketene, in the presence of a solvent and of an amine as catalyst with simultaneous distillation out of the sorbic acid and of the solvent through a rectification column with reflux, wherein the solvent is used as reflux.
It is possible and advantageous to carry out the process of the invention in such a way that all the vapours produced are cooled to crystallize the sorbic acid, the crystallized sorbic acid is removed, and part of the solvent is reheated to the overhead temperature and fed as reflux through the top of the column into the rectification column. The remaining solvent is, as was originally also the case, used to dilute the sorbic acid polymer being employed. The difference from the prior art in which the reflux necessary for the rectification consists of distillate is that the solvent is used as reflux in the process of the invention.
To achieve the purpose of the invention, it is advantageous for the solvent used as reflux to have been freed as completely as possible from the sorbic acid present in the distillate, but this is not absolutely necessary. However, as the sorbic acid content in the reflux increases there is a decrease in the advantages to be achieved with the process of the invention compared with the prior art. The invention does, however, include these less optimal embodiments.
The flow diagram 1 shows diagrammatically the distillation process used in the prior art for the polyester cleavage, in which distillate taken off at the top of the column (mixture of sorbic acid and solvent) is fed as reflux into the rectification column.
Flow diagram 2 shows diagrammatically the distillation process according to the present invention, in which the solvent which has distilled out is, after removal of the sorbic acid, fed as reflux into the rectification column.
Apart from the effect of increasing the yield, the procedure of the invention also permits an up to 30% increase in capacity, although with at least partial loss of the gain in yield. To achieve the increase in capacity in the procedure of the invention described above with solvent as reflux, part of the solvent in the input is replaced by sorbic acid polyester, i.e. less solvent is used measured by the polyester input in the distillation vessel. Only when the increase in capacity is more than 30% does the yield of sorbic acid fall again to below the yield which can be achieved with the normal procedure corresponding to the prior art.
The arrangement and procedure of the invention for the preparation of sorbic acid thus allows great flexibility in relation to the quantity produced and the plant utilization, with which very rapid responses to market requirements are possible.
The process of the invention for preparing sorbic acid can in principle be carried out as described in DE-AS 1 282 645 without, however, being restricted thereto. To this extent, express reference is made to this publication, and the description of the preparation of sorbic acid using catalytic quantities of an amine (preferably 0.5 to 10% by weight based on the polyester employed) is included in the description of the present invention (cf. concerning this the disclosure from column 3, line 31 onward, with the exception of the sections describing the use of a large excess of amine, the amine simultaneously being catalyst and entrainer for the sorbic acid (distillation)). This reference also applies to the preferred solvents, amines, ratios by weight and/or ratios of amounts of the starting materials and reaction and distillation temperatures described therein.
In particular, reference is made hereinafter to additional particularly advantageous embodiments of the process of the invention.
DE-AS 1 282 645 discloses that secondary or tertiary aliphatic, alicyclic, 5- or 6-membered heterocyclic nitrogen- and/or oxygen-containing or aliphatic-aromatic-substituted amines boiling above 100° C. under atmospheric pressure are suitable as catalysts.
Examples which can be employed very successfully are: methyloctadecylamine, dimethyloctadecylamine, dimethylhexadecylamine, dimethyltetradecylamine, dimethyldodecylamine, dibutyldodecylamine, N,N,N′,N′-tetra
Nutrinova Nutrition Specialties & Food Ingredients GmbH
ProPat L.L.C.
Puttlitz Karl
Richter Johann
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