Process for the production of terephthalic acid
Terephthalic acid is produced by oxidation of para xylene, purified in an aqueous phase and recovered by precipitating a purified product from the aqueous phase, the aqueous phase mother liquor is then cooled or evaporated to produce a further less pure precipitate and a second mother liquor and the less pure precipitate is returned to the reaction medium and/or the water of the second mother liquor is used to dissolve the crude solid and/or the second mother liquor is treated to recover water which is used to wash the precipitate recovered from the aqueous solution. The process produces better yields of terephthalic acid, reduces the use of water and reduces problems in the disposal of polluted waste water.
Latest E. I. du Pont de Nemours and Company Patents:
Claims
1. A process in which terephthalic acid is produced of oxidizing para xylene to terephthalic acid in a liquid reaction medium which comprises acetic acid and in which terephthalic acid is separated from the liquid reaction medium as a crude solid, dissolved in a liquid comprising water to produce a solution and purified by a process which comprises contacting the solution under reducing conditions with hydrogen and a heterogenous catalyst for the reduction of at least some impurities, the solution is cooled after said reduction to precipitate solid purified terephthalic acid, aqueous mother liquor is separated from the precipitate wherein;
- a) the aqueous mother liquor is treated to produce a less pure precipitate comprising terephthalic acid and a second mother liquor;
- b) the less pure precipitate is returned directly or indirectly to the reaction medium; and
- c) at least part of the said second mother liquor is, directly as such or indirectly after treatment, used to dissolve the crude solid.
2. A process in which terephthalic acid is produced by oxidizing para xylene to terephthalic acid in a liquid reaction medium which comprises acetic acid and in which terephthalic acid is separated from the liquid reaction medium as a crude solid, dissolved in a liquid comprising water to produce a solution and purified by a process which comprises contacting the solution under reducing conditions with hydrogen and a heterogenous catalyst for the reduction of at least some impurities, the solution is cooled after said reduction to precipitate solid purified terephthalic acid, aqueous mother liquor is separated from the precipitate wherein;
- a) the aqueous mother liquor is treated to produce a less pure precipitate comprising terephthalic acid and a second mother liquor;
- b) the less pure precipitate is returned directly or indirectly to the reaction medium;
- c) at least part of the second mother liquor is subjected to fractional distillation to recover water from the second mother liquor; and
- d) the recovered water is used to wash the precipitate recovered from said solution after the reduction step.
4. A process according to claim 2 in which the fractional distillation (c) is carried out in a column at a reflux ratio of 2 to 10.
5. A process according to claim 4 in which 25 to 125 theoretical plates are used.
6. A process according to claim 4 in which the mother liquor returned to the fractional distillation is fed at within 0 to 30% of the theoretical plates from the top of the column.
9. A process for the production of terephthalic acid comprising:
- in a first reactor oxidizing para xylene to terephthalic acid in a liquid reaction medium which comprises acetic acid, the reaction being accompanied by the evolution of vapor comprising acetic acid and water;
- condensing said vapor and passing part of the condensate to a distillation column for separating acetic acid and water;
- separating terephthalic acid from the liquid reaction medium as a crude solid;
- dissolving the crude terephthalic acid in a liquid comprising water to produce a solution;
- in a second reactor contacting the solution under reducing conditions with hydrogen and a heterogeneous catalyst for the reduction of at least some impurities;
- cooling the solution after said reduction to precipitate solid purified terephthalic acid;
- separating primary aqueous mother liquor from the precipitate;
- treating the primary aqueous mother liquor to produce a less pure precipitate comprising terephthalic acid and a secondary mother liquor containing dissolved contaminants including p-toluic acid;
- passing at least part of the secondary mother liquor to said distillation column for the separation of acetic acid from water;
- operating the distillation column to produce a bottom product containing acetic acid from said condensate together with p-toluic acid and other high boiling point contaminants present in the secondary mother liquor and an overhead product comprising water derived from said condensate and said secondary mother liquor; and
- supplying said bottom product to the first reactor..Iaddend..Iadd.
10. A process as claimed in claim 9 further comprising returning the less pure precipitate directly or indirectly to the reaction medium..Iaddend..Iadd.11. A process as claimed in claim 9 or 10 comprising using at least part of the water derived from the distillation column to wash said precipitate comprising purified solid terephthalic acid..Iaddend..Iadd.12. A process as claimed in claim 9 or 10 comprising using at least part of the water derived from the distillation column in the dissolution of the crude terephthalic acid to produce said
solution..Iaddend..Iadd.13. A process as claimed in claim 9 in which said distillation is carried out in a column at a reflux ratio of 20 to 10..Iaddend..Iadd.14. A process as claimed in claim 13 in which 25 to 125 theoretical plates are used in said distillation..Iaddend..Iadd.15. A process as claimed in claim 13 or 14 in which the secondary mother liquor is fed at within 0 to 30% of the theoretical plates from the top of the column..Iaddend.
2849483 | August 1958 | Ham |
3452088 | June 1969 | Olsen et al. |
3592847 | July 1971 | Gallivan et al. |
3646125 | February 1972 | Berthoux et al. |
4467111 | August 21, 1984 | Puskas et al. |
4933492 | June 12, 1990 | Schroeder et al. |
5166420 | November 24, 1992 | Shiraki et al. |
52-128344 | October 1977 | JPX |
970492 | September 1964 | GBX |
970491 | September 1964 | GBX |
1373230 | November 1974 | GBX |
Type: Grant
Filed: Apr 19, 1996
Date of Patent: Dec 22, 1998
Assignee: E. I. du Pont de Nemours and Company (Wilmington, DE)
Inventors: Eric Hindmarsh (North Yorkshire), John Arthur Turner (Middlesborough), David Parker (Middlesborough)
Primary Examiner: Samuel Barts
Law Firm: Pillsbury, Madison & Sutro, LLP Intellectual Property Group
Application Number: 8/634,991
International Classification: C07C 51215;