Optimized liquid-phase oxidation
View Patent ↗Disclosed is an optimized process and apparatus for more efficiently and economically carrying out the liquid-phase oxidation of an oxidizable compound. Such liquid-phase oxidation is carried out in a bubble column reactor that provides for a highly efficient reaction at relatively low temperatures. When the oxidized compound is para-xylene and the product from the oxidation reaction is crude terephthalic acid (CTA), such CTA product can be purified and separated by more economical techniques than could be employed if the CTA were formed by a conventional high-temperature oxidation process.
1. A process for producing terephthalic acid, said process comprising:
(a) oxidizing para-xylene in a liquid phase of a multi-phase reaction medium contained in a bubble column reactor to thereby form crude terephthalic acid, wherein said reaction medium has a maximum height (H) and a minimum width occurring above H/5 from the bottom of said reaction zone (Wmin), wherein the total upright surface area of said reactor that contacts said reaction medium is greater than 3.25 WminH; and
(b) oxidizing said crude terephthalic acid in a secondary oxidation reactor to thereby form purer terephthalic acid.
2. The process of claim 1 wherein the total upright surface area of said reactor that contacts said reaction medium is in the range of from about 3.5 WminH to about 20 WminH.
3. The process of claim 1 wherein the total upright surface area of said reactor that contacts said reaction medium is in the range of from about 4 WminH to about 15 WminH.
4. The process of claim 1 wherein the total upright surface area of said reactor that contacts said reaction medium is in the range of from 5 WminH to about 10 WminH.
5. The process of claim 1 wherein said oxidizing in said secondary oxidation reactor decreases the average concentration of 4-CBA present in said crude terephthalic acid by at least about 200 ppmw to thereby form said purer terephthalic acid.
6. The process of claim 1 wherein said crude terephthalic acid has an average 4-CBA concentration of at least about 400 ppmw and said purer terephthalic acid has an average 4-CBA concentration of less than about 400 ppmw.
7. The process of claim 1 wherein said oxidizing in said secondary oxidation reactor decreases the average concentration of 4-CBA in said crude terephthalic acid by at least about 400 ppmw to thereby form said purer terephthalic acid, wherein said crude terephthalic acid has an average 4-CBA concentration of at least about 800 ppmw and said purer terephthalic acid has an average 4-CBA concentration of less than about 250 ppmw.
8. The process of claim 1 wherein said oxidizing in said secondary oxidation reactor is carried out at an average temperature at least about 10° C. greater than the average temperature of said oxidizing in said bubble column reactor.
9. The process of claim 1 wherein said oxidizing in said bubble column reactor is carried out at an average temperature in the range of from about 125 to about 200° C., wherein said oxidizing in said secondary oxidation reactor is carried out at an average temperature in the range of from about 160 to about 240° C.
10. The process of claim 1 wherein said oxidizing in said secondary oxidation reactor is carried out at an average temperature in the range of from about 20 to about 80° C. greater than the average temperature of said oxidizing in said bubble column reactor, wherein said oxidizing in said bubble column reactor is carried out at an average temperature in the range of from about 140 to about 180° C., wherein said oxidizing in said secondary oxidation reactor is carried out at an average temperature in the range of from about 180 to about 220° C.
11. The process of claim 1 wherein a substantial portion of said crude terephthalic acid exists as solid crude terephthalic acid particles having an average BET surface area of at least about 0.6 meters squared per gram.
12. The process of claim 11 wherein said solid crude terephthalic acid particles have an average particle size in the range of from about 20 to about 150 microns.
13. The process of claim 12 wherein a substantial portion of said solid crude terephthalic acid particles are formed of a plurality of agglomeraged sub-particles having an average particle size in the range of from about 0.5 to about 30 microns.
14. The process of claim 13 wherein said solid crude terephthalic acid particles have an average particle size in the range of from about 30 to about 120 microns, wherein said sub-particles have an average particle size in the range of from about 1 to about 15 microns.
15. The process of claim 1 wherein said process further comprises recovering an initial slurry comprising a mother liquor and said crude terephthalic acid from said bubble column reactor, wherein said process further comprises replacing at least about 50 weight percent of said mother liquor in said initial slurry with a replacement solvent to thereby provide a solvent-exchanged slurry comprising said replacement solvent and said crude terephthalic acid, wherein said process further comprises introducing said solvent-exchanged slurry into said secondary oxidation reactor.
16. A process for producing terephthalic acid, said process comprising:
(a) oxidizing para-xylene in a liquid phase of a multi-phase reaction medium contained in a bubble column reactor to thereby form crude terephthalic acid, wherein said reaction medium has a maximum height (H) and a minimum width occurring above H/5 from the bottom of said reaction zone (Wmin), wherein the total upright surface area of said reactor that contacts said reaction medium is greater than 3.25 WminH; and
(b) oxidizing said crude terephthalic acid in a secondary oxidation reactor to thereby form purer terephthalic acid, wherein said oxidizing in said secondary oxidation reactor is carried out at an average temperature at least about 10° C. greater than the average temperature of said oxidizing in said bubble column reactor and decreases the average concentration of 4-CBA present in said crude terephthalic acid by at least about 200 ppmw to thereby form said purer terephthalic acid.
17. The process of claim 16 wherein the total upright surface area of said reactor that contacts said reaction medium is in the range of from about 3.5 WminH to about 20 WminH.
18. The process of claim 16 wherein the total upright surface area of said reactor that contacts said reaction medium is in the range of from about 4 WminH to about 15 WminH.