AU695571B2 - Method for recovering carboxylic acids from aqueous solutions - Google Patents

Description

Regiilatioii 3.2

AUSTRALIA

K Patents Act 1990 COMPLETE SPECIFICATION FOR A STANDARD PATIENT

ORIGINAL

Name of Applicant: GLITSCH, INC.

Ae Atual Inventors: Joseph Charles GENTRY; Timothy L. HOLMES; John Carl, AddressMcINTYRE and Ronald G. GUALY in Australia: CARTE R SMITH BEADLE 2 Railway Parade Camberwell Victoria 3124 Australia Invention Title: METHOD FOR RE COVERING CARBIOXYLIC ACIDS FROM AQUE OUS SOLUTIONS ~'-the following statement is a full description of this invention, including the best method of pcrforming it known to us 4/ Ct C U C C METHOD FOB-T REC'E NG CARBOXYLIC ACIDS FROM AQUEOUS SOLUTIONS This invention relates to methods for recovering carboxylic acids having from one to ten carbon atoms, and particularly formic acid, acetic acid, and mixtures of formic and acetic acids from aqueous solutions containing the same.

Background of the Invention A number of industrially significant processes produce as a waste product dilute solutions of short chain carboxylic acids, particularly formic .i c r r r PATENT APPLICATION Docket #12327/0248 acid and acetic acid. Typically these solutions are in the range of one to three percent acid by weight. Heretofore it has been common to discard such solutions to the environment, but present day concerns about pollution are increasingly making it necessary to clean such waste water solutions and/or to recover the acids that they contain as economically valuable byproducts of the processes.

Conventional recovery systems, such as distillation, or extractive distillation, tend to be objectionably energy intensive and uneconomical, as L well as involving process difficulties such as the formation of azeotropes and 10 difficult-to-break emulsions and the like.

There is thus a need for a method of treating waste water containing short chain carboxylic acids in a manner which will produce a waste water ~:product which needs little or no after treatment before its ultimate discharge .4 0 or reuse as process water in a plant, and which produces recovered aroxyicacis f schpurtyand qulit as to be saleable or reusable i a process plant, in an economical manner. The present invention is designed to fill that need.

Summary of the Invention Broadly considered, in accordance with the present invention, there is provided a method for recovering short chain carboxylic acids having from one to ten carbon atoms, and particularly formic acid and acetic acid and 1 PATENT APPLICATION Docket #12327/0248 mixtures thereof from dilute aqueous solutions of such acids. Typical concentrations of aqueous solutions amenable to treatment by the method of the invention are one to three percent by weight acids. In accordance with the invention, the aqueous solution is brought into liquid-liquid contact with a water immiscible high boiling trialkylphosphine oxide mixture extractant, and the acids are largely absorbed into the extractant, leaving a substantially pure water raffinate, which is then passed to further treatment, disposal or reuse. The solvent extractant, now rich in acids, is then preferably dehydrated, and the water stream resulting therefrom is preferably recycled to the incoming aqueous solution. The rich solvent is then stripped of its dissolved acids in a distillation process, and the now lean extractant solvent is returned to the liquid-liquid extraction process. If needed, the removed acids are then split into components which are essentially single species of desired purity by distillation, and are thus marketable products or products usable within a plant for other processes.

The preferred solvent extractant for use in the invention is a mixture Iof four trialkylphosphine oxides, manufactured by Cytech Industries under the trademark CYANEX 923.

The preferred solvent extractant is a mixture of four trialkylphosphine oxides as follows:

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PATENT APPLICATION Docket #12327/0248

R

3 P(O) R 2 R'P(O) RR' 2 P(O) R',P(O) Where R [CH 3 normal octyl R' [CH 3

(CH

2 normal hexyl Average Molecular Weight 348 (approximately) *9*4 0 0 *000 *0 S I 0Ir 1 Se *0 Typical properties of this solvent Trialkylphosphine oxides Appearance Specific Gravity Freezing Point Viscosity Flashpoint (Closed Cup Setaflash) Autoignition Temperature Vapor Pressure Boiling Point Solubility in Water Solubility of Water in CYANEX 923 extractant are reported as follows: 93% Colorless mobile liquid 0.88 at 23°C -5 to 0 0

C

40.0 centipoise at 25 0

C

13.7 centipoise at 182°C 218 0

C

0.09 mm Hg at 31 0

C

310°C at 5C mm Hg 10 mg/1 8 w/o When in this specification and in the accompanying claims the term "solvent consisting essentially of mixed trialkylphosphine oxides" is used, the material referred to is that just described and characterized above, and its equivalents.

In accordance with the present invention, a method for recovering carboxylic acids having from one to ten carbon atoms and particularly acetic acid and formic acid from aqueous solutions containing mixtures thereof is PATENT APPLICATION Do rket #12327/0248 provided which includes contacting the aqueous solution with a solvent consisting essentially of mixed trialkylphosphine oxides in counter current liquid-liquid extraction flow in a contacting step to thereby trainsfer acids from the aqueous solution to said solvent. This extraction produces a raffinate relatively low in acid content and a solvent relatively rich in acid content, although the acid-rich solvent contains some water. It is dehydrated by applying heat thereto to separate water therefrom in a dehydration step, thereby producing a water stream and a dehydrated rich solvent stream. The acids are stripped from the dehydrated rich solvent stream in a stripping step by applying heat thereto to produce a recycle solvent consisting essentially of mixed trialkylphosphine oxides for recycle to the liquid-liquid extraction flow described above and an acid stream. When the acid stream contains more than one acid, it is split into its constituent acids in a splitting step by distillation.

Preferably, the recycle solvent consisting essentially of mixed :trialkylphosphine oxides is recycled to said contacting step, and the water stream from dehydration of the rich solvent is recycled to the incoming aqueous solution.

In further accordance with the invention, the volume ratio of solvent consisting essentially of mixed trialkylphosphine oxides to aqueous solution during said contacting is from about one part solvent to two parts aqueous PATENT APPLICATION Docket #12327/0248 solution to about two parts solvent to one part aqueous solution. The initial concentration of acids in said aqueous solution is preferably from about onehalf percent by weight to about fifteen percent by weight, although it may be from about one percent by weight to about ten percent by weight. It is also preferred that the recycle solvent consisting essentially of mixed trialkyiphosphine oxides have an acid content less than about 0.5% by weight.

The contacting of aqueous solution with solvent consisting essentially of mixed trialkyiphosphine oxides is performed at a temperature between about 35"C and about 90'C, and more preferably at a temperature between about 50'C and about 80*C. Further, the dehydrating step is preferably S performed at a pressure of about 200 millimeters of xnercuiy absolute. It #t is preferred that the stripping be performed at a temperature w- from about 250'C tc~ about 30000 at the hottest region of said stripping step, and it is also preferred that the stripping be performed at a pressure of from about -'15 to about 50 millimeters of mercury absolute. The pressure at which said stripping is performed is desirably sufficient to avoid freezing of any acid, particularly acetic acid, during said stripping or downstream thereof.

Inodrto maximize energy efcnyha'in the recycle solvent consisting essenti~Uy of mixed trialkyiphosphine oxides from the stripping step may be transferred at least in part to the rich solvent in the dehydration u n

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PATENT APPLICATION Docket #12327/0248 hi! .101 S I ~i ml,

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li Ill C S I

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step. Also, heat in the recycle solvent consisting essentially of mixed trialkylphosphine oxides from the stripping step may be transferred at least in part to the acid stream being split into constituent acids.

Fresh solvent consisting essentially of mixed trialkylphosphine oxides for use in the process may be purified prior to being contacted with said aqueous solution, for example by water washing or by distillation.

Although several modes of operation are possible, it is preferred that the contacting be effected by dispersing the solvent consisting essentially of mixed trialkylphosphine oxides as a dispersed phase in the aqueous solution which is then the continuous phase.

Vapors vented from the dehydration and/or said stripping steps may be scrubbed with scrubbing solvent consisting essentially of mixed trialkylphosphine oxides employed in the contacting step, and acids thereby dissolved in the scrubbing solvent may thereafter be recovered therefrom.

Any solvent consisting essentially of mixed trialkylphosphine oxides which becomes entrained in the raffinate from the contacting step may be coalesced out of the raffinate, thus increasing raffinate purity and recovering solvent for reuse.

Undesirable water in the final acid products may be reduced or eliminated by providing a sidj stream which is drawn from the distillation splitting step at a region where the water concentration therein is greatest, gIlrll

I

I. I PATENT APPLICATION Docket #12327/0248 or at a region where an azeotrope is formed between water and formic acid in the course of being distilled.

Impurities in the incoming aqueous solution which may interfere with the process may be eliminated by a pretreatment in which rich solvent from the contacting step is mixed with incoming aqueous solution prior to its delivery to the contacting step and then the rich solvent and aqueous solution are separated from each other by coalescing the rich solvent from said aqueous solution, with the separated aqueous solution then being delivered to the contacting step and the separated rich solvent being a1 delivered to the dehydration step.

Impurities tending to accumulate in the recycle solvent consisting essentially of mixed trialkylphosphine oxides may be removed therefrom as It; it is in the course of being recycled. These impurities may be removed by vacuum distillation of at least a portion of the solvent, or by activated carbon filtration of at least a portion of the solvent, or by contacting at least a portion of the solvent with an ion exchange agent in the course of its being recycled. Also, the impurities may be removed by neul-ralization with a basic additive of at least a portion of the solvent for recycle in the course of its being recycled. The impurities may also be controlled by adjusting the relative flow rates of aqueous solution and recycle solvent consisting essentially of mixed trialkylphosphine oxides so that the equilibrium PATENT APPLICATION Docket #12327/0248 concentrations of impurities in the solvent and in the raffinate are each at acceptable levels.

Brief Description of the Drawings FIG. 1 is a diagrammatic flowsheet for a plant for practicing the method of the inventimu, the plant being fitted particularly for recovering and separating formic acid and acetic acid from a dilute aqueous solution; and FIG. 2 is a diagrammatic flowsheet for P. plant for practicing the method of the invention to recover and separat:7 a mixture of short chain '10 carboxylic acids, and showing certain method features which may also be t-t' Iemployed in the plant and method of FIG. 1.

Detailed Description of the Preferred Embodiments Attention is first directed to FIG. 1 which shows in simplified flow diagram form a plant arranged for the practice of thG- method of the invention. Aqueous solution or waste water containing the acids sought to be recovered is delivered to extractor 10 through input line 12. The extractor is shown as being of the rotating plate type, with a motor 14 provided to rotate the plates. Various other kinds of liquid-liquid extractor devices may be employed. The top stream out of the extractor 10 is a rich solvent stream that leaves the extractor through line 16, while the bottom PATENT APPLICATION Docket #12327/0248 f solvent are introduced nto the extractor 10 near the bottom through line the recycle solvent being delivered to line 20 through line 22 and fresh solvent, when needed, being delivered through line 24. The volume ratio of solvent and aqueous solution fed to the extractor is preferably between about one-to-two and two-to-one. The initial concentration of acids in the aqueous solution feed is from about 0.5% to about 15%, and preferably from about 1% to about 6% by weight. The operational temperatuore in the contacting step is between about 35'C and about 90'C, and preferably between about 50'C and about 80'C. The phase separation line is preferably at the top region of the extractor, and the dispersed phase is the solvent while the continuous phase is the aqueous solution.

The rich acid containing solvent is delivered through line 16 to dehydrator 26. Heat is input to the dehydrator through a reboiler system 248 I, lisand water exits the dehydrator at the top through line 30, which is provided with a condenser 32 and reflux line 34 if desired. The water stream is delivered through line 38 in a recycle circuit back to input line 12.

Alternately, the water stream may be delivered out of the plant for use or disposition elsewhere or combined with the raffinate stream. The pressure in the dehydrator is preferably about 200 millimeters of mercury absolute.

-11- PATENT APPLICATION Docket #12327/0248 Rich solvent leaves the dehydrator through line 40 which delivers it to stripper 42. In stripper 42, the acids are separated from the solvent and through application of heat through reboiler system 44, and the mixed acids exit the stripper at the top through line 46, which is provided with a condenser 48 and a recycle line 50. The mixed acids are delivered through line 52 to splitter 54. The stripped solvent leaves the bottom of stripper 42 through line 22 and is recycled to the extractor 10. The acid content of the stripped solvent for recycle is less than about 0.5% by weight. At the hottest region of the stripper, the operating temperature is from about 250°C to about 300°C, and the pressure in the stripper is from about 15 to about millimeters of mercury absolute. In any event, the stripping pressure should be such as to avoid freezing of any acids there or downstream. If desired, o part of the heat in the stripped solvent may be heat exchanged with rich solvent at the dehydrator reboiler system 28, and also, if desired, part of the heat in the stripped solvent may be hat exchanged with the bottom acid ti stream in reboiler system 66 discussed below.

The mixed acids delivered to splitter 54 through line 52 are separated in a distillation process, with formic acid exiting the splitter through line 56 and being condensed in condenser 58 and refluxed in part through line with the balance being delivered out of the plant through product line 62.

The acetic acid is delivered out of the bottom of the unit through line 64, -1 -12- PATENT APPLICATION Docket #12327/0248 and a reboiler system 66 is provided to deliver heat energy into the distillation tower or splitter 54. In accordance with the invention, a side stream 68 may be taken off the splitter at a point where the concentration of any water contaminant is at its highest; this point most usually being at a point where an a2eotrope is formed between water and the lighter acid, that is, the formic acid.

Attention is now directed to FIG. 2 which is a diagrammatic flow sheet for a plant for practicing other embodiments of the invention. In FIG.

2, pieces of equipment and lines which are identical to those in FIG. 1 are 10 given the same reference characters, and the description of those parts given i" in connection with FIG. 1 applies to the plant shown in FIG. 2 also.

o 0 The plant shown in FIG. 2 differs from that of FIG. 1 in that it is i designed to process an aqueous solution containing more than formic acid t and acetic acid from the group of carboxylic acids having from one to five carbon atoms. Thus the splitter or distillation column 54 in FIG. 2 is provided with additional side stream take-offs 100 and 102 for recovering additional acids beyond those which the distillation operation will tend to separate to the top and bottom of that tower. Those skilled in the art will appreciate that the separation of the recovered mixed acids may be effected stage-wise in a aeries of towers rather than in a single tower, if desired.

-13- PATENT APPLICATION Docket #12327/0248 It has been discovered that impurities in the waste water or input aqueous solution entering the system through line 12 may cause operational difficulties through inducing emulsification in various streams in the plant, and as well as other operating inefficiencies. In accordance with the invention, these impurities may be eliminated by an additional process step in which rich solvent leaving extractor 10 through line 16 is joined with fresh incoming aqueous solution in line 12 and these materials are passed to mixer 104, After being thoroughly mixed, the rich solvent and the incoming aqueous solution pass through line 106 to a coalescer 108 where the species separate, and rich solvent then passes through line 110 to the dehydrator 26, while acid containing water is fed through line 112 into extractor 10. In this S i manner, the impurities in the incoming aqueous solution are made more readily coalescible.

It has also been found that unexpected impurities may be in the fresh solvent which is charged to the plant at startup, or which is added to the plant in the course of operations. As appears in FIG. 2, a purifier 114 may be placed in the fresh solvent input line 24 to remove these impurities. The purifier 114 may be a distillation tower, an activated carbon bed, an ion exchange system, a water wash system, or other separating equipment.

Since the problem of impurities in the fresh solvent is most acute at startup, piping may be provided to utilize equipment of the plant during startup to A i -14- PATENT APPLICATION Docket #12327/0248 effect the removal of the impurities in the fresh solvent. For example, stripper 42 or dehydrator 26 may be temporarily so employed during startup.

Additionally, the impurities may be removed in a purifier which is a separate stand-alone plant, if desired.

As has been explained above, it is preferred that dehydrator 26 and stripper 42 be operated at vacuum. The vacuum inducing equipment is shown in FIG. 2, although it should be understood that similar equipment would be present in a plant arranged as in FIG. 1. This equipment includes j pump 116 and vent 118 in line 38 out of the top of the dehydrator 26. The c OI ,10 pump may be a mechanical pump or other vacuum inducing equipment such as a steam ejector. Since the stream through vent 118 may contain some acids and other material which would be viewed as pollutants, a scrubber 120 may be provided. Scrubber 120 may use as the scrubbing fluid the same kind of solvent as is employed in the plant as the main extractant, and the I t ttt solvent may be passed through scrubber 120 as a side loop in the main SI solvent circuit of the plant.

Similarly for tower 42, a vacuum pump 122 and vent 124 are provided. Also, a scrubber 126 is provided for removing this acid and other pollutants from the stream leaving the plant through vent 124.

As has been noted above, impurities may tend to accumulate in the solvent as it is cycled through the process. These impurities may be 1 PATENT APPLICATION Docket #12327/0248 conveniently removed from the recycle solvent passing through line 22, by drawing off at least a portion of the recycle solvent through line 130 and passing it through purifier 114, or through a separate purifier, where the impurities may be removed by vacuum distillation, activated carbon filtr L.on, ion exchange, or neutralization with a basic additive, or otherwise.

Under some operating conditions, the raffinate leaving the extractor through line 18 may have some solvent physically entrained in it. This solvent can be removed and recovered, for example in a coalescer 128. The recovered solvent may be returned to the main solvent circuit of the plant, and the raffinate, now freed of entrained solvent may be discarded, further processed, or reused in the plant.

Various features of the plant illustrated in FIG. 2 which is designed for processing multiple acids in the incoming aqueous solution stream may be incorporated into the plant shown in FIG. 1, which is designed for o processing formic acid and acetic acid only, and the converse is the case as Sbe appreciated by those skilled in the art.

will be appreciated by those skilled in the art.

6 i t

Claims (18)

1. A method for recovering acetic acid and formic acid from an aqueous solution thereof comprising: contacting said aqueous solution with solvent consisting essentially of mixed trialkylphosphine oxides in counter-current liquid-liquid extraction flow in a contacting step to thereby transfer acetic acid and formic acid from said aqueous solution to said solvent, thereby producing a raffinate relatively low in acid content and a solvent relatively rich in acid content, said acid- rich solvent containing some water; dehydrating said rich solvent by applying heat thereto to separate water therefrom in a dehydration step thereby producing a water stream and a dehydrated rich solveris stream; stripping the acetic acid and formic acid from said dehydrated rich recycle solvent stream in a stripping step by applying heat thereto to produce a solvent consisting essentially of mixed trialkylphosphine oxides for recycle to said liquid-liquid extraction flow, and an acid stream ccntaining acetic acid and formic acid; and splitting said acid stream into acetic acid and formic acid in a splitting step by distillation. ii r J lj I 11 -17- PATENT APPLICATION Docket #12327/0248 1 2. A method in accordance with Claim 1 in which said recycle 2 solvent consisting essentially of mixed trialkylphosphine oxides is recycled to 3 said contacting step. 1 3. A method in accordance with Claim 1 in which said water 2 stream from dehydration of said rich solvent is recycled to said aqueous 3 solution. 4*44 4it 1 4. A method in accordance with Claim 1 in which the volume 2 ratio of solvent consisting essentially of mixed trialkylphosphine oxides to 3 aqueous solution during said contacting is from about one part solvent to 4 two parts aqueous solution to about two parts solvent to one part aqueous solution. 1 tp 1 5. A method in accordance with Claim 1 in which the initial 2 concentration of acids in said aqueous solution is from about one percent 3 by weight to about six percent by weight. 1 6. A method in accordance with Claim 1 in which the initial 2 concentration of acids in said aqueous solution is from about one-half 3 percent by weight to about fifteen percent by weight. -18- PATENT APPLICATION Docket #12327/0248 1 7. A method in accordance with Claim 1 in which said recycle 2 solvent consisting essentially of mixed trialkylphosphine oxides has an acid 3 content less than about 0.5% by weight. 1 8. A method in accordance with Claim 1 in which said contacting 2 of aqueous solution with solvent consisting essentially of mixed 3 trialkylphosphine oxides is performed at a temperature between about 35 C .4 and about S* t I 4' 0 S. 1 9. A method in accordance with Claim 1 in which said contacting o% 2 of aqueous solution with solvent consisting essentially of mixed 3 trialkylphosphine oxides is performed at a temperature between about 4 and about 1 10. A method in accordance with Claim 1 in w'uth 4aid 2 dehydrating step is performed at a pressure of about 200 nmilimeters of 3 mercury absolute. 1 11. A method in accordance with Claim 1 in which said stripping 2 is performed at a temperature of from about 250C to about 300°C at the 3 hottest region of said stripping step.

4. -19- PATENT APPLICATION Docket #12327/0248 1 12. A method in accordance with Claim I in which said stripping 2 is performed at a pressure of from about 15 to about 50 millimeters of 3 mercury absolute. 1 13. A method in accordance with Claim 12 in which the 2 temperature and pressure at which said stripping is performed is sufficient 3 to avoid freezing of said acetic acid during said stripping or downstream 4 thereof. S 1 14 A method in accordance with Claim 1 in which heat in said 2 recycle solvent consisting essentially of mixed trialkylphosphine oxides from 3 said stripping step is transferred at least in part to said rich solvent in said 4 dehydration step. 1 15. A method in accordance with Claim 1 in which heat in said 2 recycle solvent consisting essentially of mixed trialkylphosphine oxides from 3 said stripping step is transferred at least in part to said acid stream being 4 split into acetic acid and formic acid. PATENT APPLICATION Docket #12327/0248 1 16. A method in accordance with Claim 1 in which said contacting 2 is effected by dispersing said solvent consisting essentially of mixed 3 trialkylphosphine oxides as a dispersed phase in said aqueous solution as a 4 continuous phase. 1 17. A method in accordance with Claim 1 in which fresh solvent 2 consisting essentially of mixed trialkylphosphine oxides is purified prior to 3 being contacted with said aqueous solution. I 49*

18. A method in accordance with Claim 17 in which fresh solvent 2 consisting essentially of mixed trialkylphosphine oxides is purified by water 3 washing. 3 distillation. i 20. A method in accordance with Claim 1 in which vapors vented 2 from said dehydration and/or said stripping steps are scrubbed with 3 scrubbing solvent consisting essentially of mixed trialkylphosphine oxides 4 employed in said contacting step. j SI -21- PATENT APPLICATION Docket #12327/0248 1 21. A method in accordance with CJim 1 in which vapors vented S2 from said dehydration and/or said stripping steps are scrubbed with 3 scrubbing solvent consisting essentially of mixed trialkylphosphine oxides. 4 and acids thereby dissolved in said scrubbing solvent are thereafter recovered therefrom.

22. A method in accordance with Claim 1 in which any solvent 2 consisting essentially of mixed trialkviphosphine oxides entrained in said 3 raffinate from said contacting step is coalesced out of said raffinate. P 1 23. A method in accordance with Claim 1 in which a side stream 2 is drawn from said distillation splitting step at a region where the water 3 concentration therein is greatest. 1 24. A method in accordance with Claim 1 in which a side stream 2 is drawn from said distillation splitting step at a region where an azeotrope 3 is formed between water and formic acid in the course of being distilled. 1 25. A method in accordance with Claim 1 in which rich solvent 2 from said contacting step is mixed with said aqueous solution prior to its 3 delivery to said contacting step and then said rich solvent and aqueous I~C~~q~ 1 3 at.. atta a Pt t j.t 4 tat. a a 3 1 3 4 -22- PATENT APPLICATION Docket #12327/0248 solution are separated from each other by coalescing said rich solvent from said aqueous solution, with said separated aqueous solution being delivered to said contacting step and said separated rich solvent being delivered to said dehydration step.

26. A method in accordance with Claim 2 in which impurities tending to accumulate in said recycle solvent consisting essentially of mixed trialkylphosphine oxides are removed therefrom in the course of its being recycled.

27. A method in accordance with Claim 26 in which said impurities are removed by vacuum distillation of at least a portion of said recycle solvent consisting essentially of mixed trialkylphosphine oxides in the course of its being recycled.

28. A method in accordance with Claim 26 in which said impurities are removed by activated carbon filtration of at least a portion of said recycle solvent consisting essentially of mixed trialkylphosphine oxides in the course of its being recycled. r r ri ii I I ~II_~1.XUD- SYII~- r_ 1I-- II~ -23- PATENT APPLICATION Docket #12327/0248 oD~ eco *o o sees o c «o o e81€ Ii

29. A method in accordance with Claim 26 in which said impurities are removed by contacting at least a portion of said recycle solvent consisting essentially of mixed trialkylphosphine oxides with an ion exchange agent in the course of its being recycled.

30. A method in accordance with Claim 26 in which said impurities are removed by neutralization with a basic additive of at least a portion of said recycle solvent consisting essentially of mixed trialkylphosphine oxides in the course of its being recycled.

31. A method in accordance with Claim 2 1 which said impurities are controlled by adjusting the relative flow rates or aqueous solution and recycle solvent consisting essentially of mixed trialkylphosphine oxides so that the equilibrium concentra:ions of impurities in said solvent consisting essentially of mixed trialkylphosphine oxides for recycle and in said raffinate are each at acceptable levels.

32. A method for recovering carboxyiic acids from an aqueous solution containing at least one acid from the group consisting of carboxylic acids having from one to ten carbon atoms comprising: 1 2 3 4 6 L- l-r~ -24- PATENT APPLICATION Docket #12327/0248 4 contacting said aqueous solution with solvent consisting essentially of mixed trialkylphosphine oxides in counter-current liquid-liquid extraction 6 flow in a contacting step to thereby transfer said acids from said aqueous 7 solution to said solvent, thereby producing a raffinate relatively low in acid 8 content and a solvent relatively rich in acid content, said acid-rich solvent 9 containing some water; dehydrating said rich solvent by applying heat thereto to separate 11 water therefrom in a dehydration step thereby producing a water stream and a c 12 a dehydrated rich solvent stream; and *0 0 13 stripping the acids from said dehydrated rich solvent stream in a 14 stripping step by applying heat thereto to produce a recycle solvent 15 consisting essentially of mixed trialkylphosphine oxides for recycle to said 16 liquid-liquid extraction flow and an acid stream containing said acids. 1 33. A method in accordance with Claim 32 in which said aqueous 1, 2 solution contains at least two carboxylic acids and further comprising 3 splitting said acid stream into individual acids in a splitting step by 4 distillation. u" n. PATENT APPLICATION Docket #12327/0248 re:

34. A method in accordance with Claim 32 in which said solvent consisting essentially of mixed trialkylphosphine oxides for recycle is recycled to said contacting step. A method in accordance with Claim 32 in which said water stream from dehydration of said rich solvent is recycled to said aqueous solution.

36. A method in accordance with Claim 32 in which the volume ratio of solvent consisting essentially of mixed trialkylphosphine oxides to aqueous solution during said contacting is from about one part solvent to two parts aqueous solution to about two narts solvent to one part aqueous solution.

37. A method in accordance with Claim 32 in which the initial concentration of acids in said aqueous solution is from about one percent by weirh: :o about six percent by weight.

38. A method in accordance with Claim 32 in which the initial concentration of acids in said aqueous solution is from about one-half percent by weight to about fifteen percent by weight. I i -26- PATENT APPLICATION Docket #12327/0248

39. A method in accordance with Claim 32 in which said solvent consisting essentially of mixed trialkylphosphine oxides for recycle has an acid content less than about 0.5% by weight.

40. A method in accordance with Claim 32 in which said contacting of aqueous solution with solvent consisting essentially of mixed trialkylphosphine oxides is performed at a temperature between about and about 90 0 C. o 4 0 ar U U 1 2 3 4 1 41. A method in accordance with Claim 32 in which said 2 contacting of aqueous solution with solvent consisting essentially of mixed 3 trialkylphosphine oxides is performed at a temperature between about 4 and about 800C. 1 42. A method in accordance with Claim 32 in which said 2 dehydrating step is performed a: a pressure of about 200 millimeters of 3 mercury absolute. 1 43. A method.in accordance with Claim 32 in which said stripping 2 is performed at a temperature of from about 250*C to about 300"C at the 3 hottest region of said stripping step. -27- PATENT APPLICATION Docket #12327/0248 1 44. A method in accordance with Claim 32 in which said stripping 2 is performed at a pressure of from about 15 to about 50 millimeters of 3 rncrcurv absolute. 1 45. A method in accordance with Claim 44 in which the 2 mperature and pressure at which said stripping is performed is sufficient 3 to avoid freezing of said any acid during said stripping or downstream 4 thereof. Cf

146. A method in accordance with Claim 32 in which heat in said recycle solvent consisting essentially of mixed trialkyiphosphine oxides from It3 said stripping step is trantsferred at least in part to said rich solvent in said *I4 dehydration step. 1 47. A method in accordance with Claim 32 in which heat in said 2 recycle solvent consisting essentially of mixed trialkylphosphine oxides from 3 said stripping step is transferred at least in part to said acid stream being I 4 split into its constituent acids. -28- PATENT APPLICATION Docket #12327/0248 1 48. A method in accordance with Claim 32 in which said 2 contacting is effected by dispersing said solvent consisting essentially of 3 mixed trialkylphosphine oxides as a dispersed phase in said aqueous solution 4 as a continuous phase. I d9. A method in accordance with Claim 32 in which fresh solvent 2 consisting essentially of mixed trialkylphosphine oxides is purified prior to 3 being contacted with said aqueous solution. (I 1 50. A method in accordance with Claim 49 in which fresh solvent 2 consisting essentially of mixed trialkylphosphine oxides is purified by water 3 washing. 1 51. A method in accordance with Claim 49 in which fresh solvent 2 consisting essentially of mixed trialkylphosphine oxides is purified by 3 distillation. 1 52. A method in accordance with Claim 32 in which vapors vented 2 from said dehydration and/or said stripping steps are scrubbed with 3 scrubbing solvent consisting essentially of mixed trialkylphosphine oxides 4 employed in said contacting step. i- -29- PATENT APPLICATION Docket #12327/0248 1 53. A method in accordance with Claim 32 in which vapors vented 2 from said dehydration and/or said stripping steps are scrubbed with 3 scrubbing solvent consisting essentially of mixed trialkylphosphine oxides, 4 and acids thereby dissolved in said scrubbing solvent are thereafter recovered therefrom. 1 54. A method 1 accordance with Claim 32 in which any solvent 2 consisting essentially of mixed trialkylphosphine oxides entrained in said 3 raffinate from said contacting step is coalesced out of said raffinate. 1 55. A method in accordance with Claim 32 in which a side stream 2 is drawn from said distillation splitting step at a region where the water 3 concentration therein is greatest. Si 1 56. A method in accordance with Claim 32 in which a side stream 2 is drawn from said distillation splitting step at a region where an azeotrope 3 is formed between water and formic acid in the course of being distilled. 1 57. A method in accordance with Claim 32 in which rich solvent 2 from said contacting step is mixed with said aqueous solution prior to its 3 delivery to said contacting step and then said rich solvent and aqueous 1f"" PATENT APPLICATION Docket #12327/0248 solution are separated from each other by coalescing said rich solvent fr.m said aqueous solution, with said separated aqueous solution being delivered to said contacting step and said separated rich solvent being delivered to said dehydration step. 58. A method in accordance with Claim 34 in which impurities tending to accumulate in said recycle solvent consisting essentially of mixed trialkylphosphine oxides are removed therefrom in the course of its being recycled. 59. A method in accordance with Claim 58 in which said impurities are removed by vacuum distillation of at least a portion of said recycle solvent consisting essentially of mixed trialkylphosphine oxides in the course of its being recycled. t i i A method in accordance with Claim 58 in which said impurities are removed by activated carbon filtration of at least a portion of said recycle solvent consisting essentially oi mixed trialkylphosphine oxides in the course of its being recycled. -31- PATENT APPLICATION Docket #12327/0248 1 61. A method in accordance with Claim 58 in which said 2 impurities are removed by contacting at least a portion of said solvent 3 consisting essentially of mixed trialkylphosphine oxides for recycle with an 4 ion exchange agent in the course of its being recycled. I 62. A method in accordance with Claim 58 in which said 2 impurities are removed by neutralization with a basic additive of at least a 3 portion of said solvent consisting essentially of mixed trialkylphosphine 4 oxides for recycle in the course of its being recycled. 1 63. A method in accordance with Claim 34 in which said 2 impurities are controlled by adjusting the relative flow rates of aqueous 3 solution and recycle solvent consisting essentially ji mixed trialkylphosphine S 4 oxides so that the equilibrium corcentrarions of impurities in said solvent t tt consisting essentially of aixed trialkylphosphine oxides for recycle and in t I 6 said raffinate are each at acceptable levels. t t *DATED: 25 June 1998 CARTER SMITH BEADLE Patent Attorneys ibr the Applicant: GLITSCH, INC. n~ l -r rri*l i ~Z k -4*Cll.r ycllrcrsrr=~2~nrrrcsi--=i=~C LI~I SPATENT APPLICATION Docket #12327/0248 ABSTRACT Disclosed is a method for recovering carboxylic acids having from one to ten carbon atoms, and particularly formic acid, acetic acid and mixtures of formic and acetic acids, from aqueous solutions, in which the aqueous solution is contacted with solvent consisting essentially of mixed trialkylphosphine oxides in counter-current liquid-liquid extraction flow in a contacting step to thereby transfer the acids from the aqueous solution to S, the solvent, thus producing a raffinate relatively low in acid content and a rich solvent. The rich solvent is preferably dehydrated to separate water S 10 therefrom and yield a dehydrated rich solvent. The dehydrated rich solvent then has the acids stripped from it and the resulting lean solvent is then returned to the liquid-liquid extraction step, while the separated acids are split into their constituent components in a distillation operation. T