WO2010032263A2 - Process and equipment for recovery of valuable materials from terephthalic acid manufacture - Google Patents
Process and equipment for recovery of valuable materials from terephthalic acid manufacture Download PDFInfo
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- WO2010032263A2 WO2010032263A2 PCT/IN2009/000468 IN2009000468W WO2010032263A2 WO 2010032263 A2 WO2010032263 A2 WO 2010032263A2 IN 2009000468 W IN2009000468 W IN 2009000468W WO 2010032263 A2 WO2010032263 A2 WO 2010032263A2
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- Prior art keywords
- dilution
- outlet
- tank
- chilling
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- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 title claims abstract description 60
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 28
- 238000011084 recovery Methods 0.000 title claims abstract description 22
- 239000000463 material Substances 0.000 title claims abstract description 19
- 238000000034 method Methods 0.000 title claims abstract description 18
- 238000010790 dilution Methods 0.000 claims abstract description 41
- 239000012895 dilution Substances 0.000 claims abstract description 41
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 34
- 239000003054 catalyst Substances 0.000 claims abstract description 32
- 239000008346 aqueous phase Substances 0.000 claims abstract description 21
- 238000007254 oxidation reaction Methods 0.000 claims abstract description 14
- 230000003647 oxidation Effects 0.000 claims abstract description 12
- 239000007790 solid phase Substances 0.000 claims abstract description 9
- 150000002894 organic compounds Chemical class 0.000 claims abstract description 8
- 238000003756 stirring Methods 0.000 claims abstract description 5
- 238000007865 diluting Methods 0.000 claims abstract description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 30
- 239000012528 membrane Substances 0.000 claims description 26
- 239000007788 liquid Substances 0.000 claims description 21
- 238000001556 precipitation Methods 0.000 claims description 16
- 239000007787 solid Substances 0.000 claims description 13
- 239000003513 alkali Substances 0.000 claims description 11
- 230000008929 regeneration Effects 0.000 claims description 11
- 238000011069 regeneration method Methods 0.000 claims description 11
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 8
- 238000000926 separation method Methods 0.000 claims description 8
- 238000003860 storage Methods 0.000 claims description 8
- 238000001704 evaporation Methods 0.000 claims description 4
- 230000008020 evaporation Effects 0.000 claims description 4
- 239000002244 precipitate Substances 0.000 claims description 4
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 4
- 235000017550 sodium carbonate Nutrition 0.000 claims description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 3
- 238000001914 filtration Methods 0.000 claims description 3
- 229910017052 cobalt Inorganic materials 0.000 description 7
- 239000010941 cobalt Substances 0.000 description 7
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 7
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 6
- 238000013019 agitation Methods 0.000 description 6
- 229910052748 manganese Inorganic materials 0.000 description 6
- 239000011572 manganese Substances 0.000 description 6
- 239000012452 mother liquor Substances 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000012141 concentrate Substances 0.000 description 3
- 239000002826 coolant Substances 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 239000000706 filtrate Substances 0.000 description 3
- 239000011368 organic material Substances 0.000 description 3
- 239000012466 permeate Substances 0.000 description 3
- 238000001223 reverse osmosis Methods 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000002351 wastewater Substances 0.000 description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 238000010926 purge Methods 0.000 description 2
- 239000013049 sediment Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000005711 Benzoic acid Substances 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 229940011182 cobalt acetate Drugs 0.000 description 1
- NXTZRSCVEDUAGZ-UHFFFAOYSA-J cobalt(2+);manganese(2+);tetrabromide Chemical compound [Mn+2].[Co+2].[Br-].[Br-].[Br-].[Br-] NXTZRSCVEDUAGZ-UHFFFAOYSA-J 0.000 description 1
- QAHREYKOYSIQPH-UHFFFAOYSA-L cobalt(II) acetate Chemical compound [Co+2].CC([O-])=O.CC([O-])=O QAHREYKOYSIQPH-UHFFFAOYSA-L 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 229910000042 hydrogen bromide Inorganic materials 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 229940071125 manganese acetate Drugs 0.000 description 1
- UOGMEBQRZBEZQT-UHFFFAOYSA-L manganese(2+);diacetate Chemical compound [Mn+2].CC([O-])=O.CC([O-])=O UOGMEBQRZBEZQT-UHFFFAOYSA-L 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 230000003134 recirculating effect Effects 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/04—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing carboxylic acids or their salts
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D61/00—Processes of separation using semi-permeable membranes, e.g. dialysis, osmosis or ultrafiltration; Apparatus, accessories or auxiliary operations specially adapted therefor
- B01D61/02—Reverse osmosis; Hyperfiltration ; Nanofiltration
- B01D61/025—Reverse osmosis; Hyperfiltration
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D61/00—Processes of separation using semi-permeable membranes, e.g. dialysis, osmosis or ultrafiltration; Apparatus, accessories or auxiliary operations specially adapted therefor
- B01D61/02—Reverse osmosis; Hyperfiltration ; Nanofiltration
- B01D61/025—Reverse osmosis; Hyperfiltration
- B01D61/026—Reverse osmosis; Hyperfiltration comprising multiple reverse osmosis steps
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D61/00—Processes of separation using semi-permeable membranes, e.g. dialysis, osmosis or ultrafiltration; Apparatus, accessories or auxiliary operations specially adapted therefor
- B01D61/02—Reverse osmosis; Hyperfiltration ; Nanofiltration
- B01D61/04—Feed pretreatment
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/40—Regeneration or reactivation
- B01J31/4015—Regeneration or reactivation of catalysts containing metals
- B01J31/4023—Regeneration or reactivation of catalysts containing metals containing iron group metals, noble metals or copper
- B01J31/403—Regeneration or reactivation of catalysts containing metals containing iron group metals, noble metals or copper containing iron group metals or copper
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/40—Regeneration or reactivation
- B01J31/4015—Regeneration or reactivation of catalysts containing metals
- B01J31/4053—Regeneration or reactivation of catalysts containing metals with recovery of phosphorous catalyst system constituents
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J38/00—Regeneration or reactivation of catalysts, in general
- B01J38/48—Liquid treating or treating in liquid phase, e.g. dissolved or suspended
- B01J38/60—Liquid treating or treating in liquid phase, e.g. dissolved or suspended using acids
- B01J38/62—Liquid treating or treating in liquid phase, e.g. dissolved or suspended using acids organic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/41—Preparation of salts of carboxylic acids
- C07C51/412—Preparation of salts of carboxylic acids by conversion of the acids, their salts, esters or anhydrides with the same carboxylic acid part
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/42—Separation; Purification; Stabilisation; Use of additives
- C07C51/43—Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/42—Separation; Purification; Stabilisation; Use of additives
- C07C51/47—Separation; Purification; Stabilisation; Use of additives by solid-liquid treatment; by chemisorption
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/42—Separation; Purification; Stabilisation; Use of additives
- C07C51/487—Separation; Purification; Stabilisation; Use of additives by treatment giving rise to chemical modification
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2311/00—Details relating to membrane separation process operations and control
- B01D2311/04—Specific process operations in the feed stream; Feed pretreatment
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2317/00—Membrane module arrangements within a plant or an apparatus
- B01D2317/02—Elements in series
- B01D2317/025—Permeate series
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2317/00—Membrane module arrangements within a plant or an apparatus
- B01D2317/02—Elements in series
- B01D2317/027—Christmas tree arrangements
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2317/00—Membrane module arrangements within a plant or an apparatus
- B01D2317/04—Elements in parallel
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/16—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/32—Manganese, technetium or rhenium
- B01J23/34—Manganese
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/74—Iron group metals
- B01J23/75—Cobalt
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/70—Complexes comprising metals of Group VII (VIIB) as the central metal
- B01J2531/72—Manganese
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
- B01J2531/84—Metals of the iron group
- B01J2531/845—Cobalt
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/584—Recycling of catalysts
Definitions
- This invention relates to a process and equipment for recovery of valuable materials from terephthalic acid manufacture.
- Terephthalic acid is manufactured by liquid-phase oxidation of p-xy ⁇ ene with air over cobalt- manganese-bromide catalyst system (cobalt acetate, manganese acetate, and hydrogen bromide) in acetic acid at 150 to 210 °C.
- cobalt- manganese-bromide catalyst system cobalt acetate, manganese acetate, and hydrogen bromide
- the relative weight ratio of cobalt, manganese and bromine are important, and the typical values are manganese: cobalt ratio 3:1 and cobalt: bromine ratio 1 :5.
- the reactor and crystallizer of the terephthalic acid manufacturing plant most of the terephthalic acid crystallizes out from the mother liquor and is separated by filtration.
- the mother liquor comprises mainly acetic acid and organic compounds like isopthalic acid, benzoic acid and terephthalic acid, and inorganic compounds like cobalt and manganese along with iron, nickel, chromium and sodium. It is a common practice to recycle a large portion of the recovered mother liquor to the oxidation reaction in order to recover the catalyst partially and promote the oxidation reaction while purging a small portion to a solvent recovery system so as to maintain the level of impurities and by-products in the reaction within tolerable limits.
- mother liquor purge is subjected to evaporation to remove considerable portion of acetic acid and water leaving behind a concentrate containing organic compounds together with heavy metal catalysts.
- the concentrate hereinreferred to as reactor effluent is disposed of by incineration usually in furnaces.
- An object of the invention is to provide a process for recovery of valuable materials from the reactor effluent from terephthalic acid manufacture.
- Another object of the invention is to provide an equipment for recovery of valuable materials from the reactor effluent from terephthalic acid manufacture.
- a process for recovery of valuable materials from terephthalic acid manufacture comprising the steps of diluting the reactor effluent from terephthalic acid manufacture with water in the weight ratio 1 : 1 to 1 :12 and chilling the dilution of the effluent to 5 to 20°C under stirring; separating the aqueous phase rich in the spent oxidation catalyst from the solid phase rich in organic compounds; and concentrating the aqueous phase to recover the spent oxidation catalyst and water.
- the dilution of the effluent with water is carried out in the weight ratio 1 :10 and the dilution of the effluent is chilled at 5-15°C.
- the separation of aqueous phase and solid phase is carried out by solid-liquid separation method.
- concentration of the aqueous phase is carried out by evaporation of the aqueous phase.
- concentration of the aqueous phase is carried out by precipitation by treatment with an alkali to adjust the pH between 7 and 8 under stirring followed by separation of the precipitate by filtration.
- the alkali is soda ash and preferably the precipitate is treated with acetic acid to convert the spent oxidation catalyst into acetate.
- the concentration of the aqueous phase is carried out by membrane separation method.
- an equipment for recovery of valuable materials from terephthalic acid manufacture comprising a jacketed dilution cum chilling tank provided with a stirrer and connected to an inlet line for the reactor effluent from the terephthalic acid manufacture and to a dilution water inlet line, the jacket of the dilution cum chilling tank being connected to a chilling unit, a solid-liquid separator the inlet of which is connected to the outlet of the dilution cum chilling tank, a flasher drum provided with a reboiler and connected to the outlet of the solid liquid separator and a condenser the inlet of which is connected to the vapour outlet of the flasher drum.
- an equipment for recovery of valuable materials from terephthalic acid manufacture comprising a jacketed dilution cum chilling tank provided with a stirrer and connected to an inlet line for the reactor effluent from the terephtalic acid manufacture and to a dilution water inlet line, the jacket of the dilution cum chilling tank being connected to a chilling unit, a solid-liquid separator the inlet of which is connected to the outlet of the dilution cum chilling tank, a precipitation tank provided with a stirrer and connected to the outlet of the solid liquid separator, the precipitation tank being further provided with an alkali dosing line and a CO 2 outlet line, a filter the inlet of which is connected to the outlet of the precipitation tank and a catalyst regeneration tank provided with a stirrer and connected to the outlet of the filter, the catalyst regeneration tank being further provided with an acetic acid dosing line, CO 2 outlet line and a recovered catalyst outlet line.
- an equipment for recovery of valuable materials from terephthalic acid manufacture comprising a jacketed dilution cum chilling tank provided with a stirrer and connected to an inlet line for the reactor effluent from the terephthalic acid manufacture and to a dilution water inlet line, the jacket of the dilution cum chilling tank being connected to a chilling unit, a solid-liquid separator the inlet of which is connected to the outlet of the dilution cum chilling tank and a storage tank the inlet of which is connected to the outlet of the solid liquid separator and the outlet of which is connected to a membrane separator array means.
- Fig 1 is a flow diagram of the equipment for recovering valuable materials from the reactor effluent from terephthalic acid manufacture according to an embodiment of the invention
- Fig 2 is a flow diagram of the equipment for recovering valuable materials from the reactor effluent from terephthalic acid manufacture according to another embodiment of the invention.
- Fig 3 is a flow diagram of the equipment for recovering valuable materials from the reactor effluent from terephthalic acid manufacture according to another embodiment of the invention.
- the equipment IA as illustrated in Fig 1 of the accompanying drawings comprises a jacketed dilution cum chilling tank 2 provided with a stirrer 3.
- the jacket of the tank is marked 4.
- 5 is a chilling unit for recirculating a coolant (not shown) in the jacket of the tank 2 via recirculation lines marked 6 and 7.
- the tank 2 is connected to a reactor effluent inlet line 8 and a dilution water inlet line 9.
- 10 is a solid liquid separator the inlet of which is connected to the outlet of the tank 2 via line 11. Sediment outlet line of the solid liquid separator is marked 12.
- 13 is a flasher drum, the recovered catalyst discharge line of which is marked 14.
- 15 is a reboiler provided with the flasher drum.
- 16 is a condenser the inlet of which is connected to the vapour outlet of the flasher drum via line 17.
- the outlet of the condenser is connected to a recovered water line 18 which in turn is connected to the dilution water inlet line 9.
- Coolant inlet and outlet of the condenser are marked 19 and 20 respectively.
- Reactor effluent (not shown) at about 80 to 9O 0 C from terephthalic acid manufacturing plant (not shown) is fed into the tank 2 via effluent inlet line 8.
- Dilution water (not shown) is fed into the tank 2 via dilution water inlet line 9.
- Dilution of the effluent is carried out with water in the tank 2 in the weight ratio 1 :1 to 1 :12 preferably 1 :10 under agitation with the stirrer 3.
- the effluent dilution in the tank 2 is chilled at 5-20 0 C, preferably 5-15°C by circulating coolant (not shown) from the chilling unit in the jacket of the tank 2. Due to dilution and chilling the organic compounds present in the effluent solidify.
- the aqueous phase rich in spent oxidation catalyst is separated from the solid phase rich in organic compounds in the solid liquid separator.
- the solid phase is discharged through the sediment outlet line 12.
- the aqueous phase is flashed in the flasher drum.
- the reboiler reboils the aqueous phase and feeds into the flasher drum.
- the concentrate rich in the spent oxidation catalyst is collected via the recovered catalyst discharge line 14.
- the vapour phase mainly containing water is fed into the condenser 16 via line 17 and is condensed in the condenser.
- the water recovered in the condenser is fed into the tank 2 via the recovered water line 18.
- the equipment IB as illustrated in Fig 2 of the accompanying drawings comprises a precipitation tank 21 provided with a stirrer 22.
- 23 is an alkali dosing line provided with the precipitation tank.
- 24 is the CO 2 gas outlet of the precipitation tank.
- the precipitation tank is connected to the outlet of the solid liquid separator via line 25.
- 26 is a filter connected to the outlet of the precipitation tank via line 26a.
- 27 is the filtrate outlet line of the filter.
- 28 is a catalyst regeneration tank the inlet of which is connected to the outlet of the filter via line 27a.
- the regeneration tank 28 is provided with a stirrer 29.
- 30 is an acetic acid dosing line provided with the regeneration tank.
- 31 is the CO 2 gas outlet of the regeneration tank.
- 32 is the recovered catalyst outlet line of the regeneration tank.
- the aqueous phase from the solid liquid separator is treated in the precipitation tank 21 with an alkali preferably soda ash under agitation to precipitate the organic catalyst.
- the precipitation is carried out at a pH of 7-8.
- the slurry comprising the spent catalyst is filtered in the filter and the solid phase is fed into the regeneration tank.
- the filtrate namely the recovered water is drained out via the filtrate outlet line 27.
- the catalyst is converted into the acetate in the regeneration tank by treatment with acetic acid under agitation and collected via the outlet line 32.
- the equipment 1 C as illustrated in Fig 3 of the accompanying drawings comprises a storage tank 33 the inlet of which is connected to the outlet of the solid liquid separator 10 via line 34.
- a plurality of membrane separators are marked 35, 36, 37 and 38.
- the inlet of membrane separator 35 is connected to the oulet of storage tank 33 via line 39.
- Reject line 40 of membrane separator 35 is connected to a wash tank 41 which in turn is connected to the inlet of membrane separator 36 via line 42.
- 43 is a reject storage tank connected to the reject line 44 of membrane separator 36 and further connected to the inlet of membrane separator
- 46 is a revocered catalyst storage tank connected to membrane separator 37 via line 47a. Recovered catalyst outlet line of the storage tank 46 is marked 47b.
- the outlet lines marked 48, 49 and 50 of membrane separators 35, 36 and 37, respectively are connected to the inlet of membrane separator 38 via line 51.
- 52 is an alkali dosing line connected across line 51 close to the inlet of membrane separator 38.
- 53 is a recovered water line connected to the outlet of membrane separator 38 and to dilution water inlet line 9.
- 54 is a cross line connected to line 53 and to wash tank 41.
- 55 is the waste water outlet line of the membrane separator 38.
- Aqueous phase from the solid liquid separator 10 is stored in tank 33.
- the aqueous phase undergoes reverse osmosis in membrane separator 35.
- the solid phase containing the spent catalyst is washed in wash tank 41 and subjected to further osmosis in membrane separator 36.
- the reject from membrane separator 36 is stored in storage tank 43 and fed into membrane separator 37.
- the reject is further subjected to reverse osmosis in membrane separator 37.
- the recovered catalyst is collected and stored in tank 46 and recovered via outlet line 47b.
- the permeates from membrane separators 35, 36 and 37 is further subjected to reverse osmosis in membrane separator 38.
- the feed going into the membrane separator 38 is dosed with an alkali preferably caustic soda so as to solidify the organic compounds, if any.
- the alkali treatment is carried out to adjust the pH between 7 and 8.
- the waste water is discharged via waste water outlet line 55 and the recovered water is partly fed into inlet line 9 and partly fed into wash tank 41.
- Example 1 In a typical equipment of Fig 1 of the accompanying drawings, reactor effluent (50 litres) at 9O 0 C was diluted with water in the weight ratios of 1 :1, 1 :2, 1 :5, 1 :8, 1 :10 and 1 : 12 under agitation and chilled to 10°C. The percentages of recovery of organic materials like cobalt and manganese were 9, 21, 53, 77, 91, 92 and 10, 25, 62, 85, 94, 99, respectively. (b) To maintain the level of impurities of organic materials and by-products in the reactor within tolerable limits, a few experiments were carried by varying the chilling temperature of the reactor effluent to 5°C, 10°C, and 15°C. The overall percentage recovery of the organic materials was found to be 80, 84 and 87, respectively.
- reactor effluent 50 litres
- water in the weight ratio of 1 :10 under agitation and chilled to 10°C.
- Precipitation of the organic catalyst was carried out with soda ash addition till pH of the solution became 7 to 8.
- Further acetic acid addition was carried out to convert the carbonates into acetates.
- the percentages recovery of cobalt and manganese were found to be 95 and 94, respectively.
- reactor effluent 50 litres at 90°C was diluted in the weight ratio of 1:10 under agitation and chilled to 10°C.
- the percentages of recovery of cobalt and manganese were found to be 98 and 99, respectively.
- Water was also recovered by precipitating the remaining organics from the permeate of the first three membrane separators by adding caustic till the pH of the permeate became 7 to 8 and then passing the solution through the fourth membrane separator. The percentage recovery of water was found to be in the range of 35 to 40.
Abstract
Description
Claims
Priority Applications (2)
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CN2009801337289A CN102137707B (en) | 2008-08-26 | 2009-08-26 | Process and equipment for recovery of valuable materials from terephthalic acid manufacture |
BRPI0918260 BRPI0918260B1 (en) | 2008-08-26 | 2009-08-26 | process and equipment for the recovery of valuable terephthalic acid preparation materials |
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IN1794MU2008 | 2008-08-26 | ||
IN1794/MUM/2008 | 2008-08-26 |
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CN (1) | CN102137707B (en) |
BR (1) | BRPI0918260B1 (en) |
PL (1) | PL217166B1 (en) |
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WO (1) | WO2010032263A2 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102381964A (en) * | 2010-09-01 | 2012-03-21 | 天华化工机械及自动化研究设计院 | Integral process for washing and filtering terephthalic acid and water recovery |
WO2015022493A1 (en) * | 2013-08-14 | 2015-02-19 | Johnson Matthey Davy Technologies Limited | Process for recovering water, metal and organics from the production of polycarboxylic acid |
WO2016005920A3 (en) * | 2014-07-09 | 2016-03-10 | Reliance Industries Limited | Method for recovery of ionic liquid and system thereof |
US9776943B2 (en) | 2014-02-20 | 2017-10-03 | Reliance Industries Limited | Catalyst recovery and recycling process during aromatic carboxylic acid production |
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US3170768A (en) * | 1959-04-22 | 1965-02-23 | Standard Oil Co | System for continuous preparation of terephthalic acid |
GB1460941A (en) * | 1973-03-30 | 1977-01-06 | Matsuyama Petrochemicals Inc | Method of recovering cobalt and or manganese-bromine liquid- phase oxidation catalyst |
WO1985002353A1 (en) * | 1983-11-30 | 1985-06-06 | Ecolochem, Inc. | Recovery of organic acids, catalysts and water from terephthalic acid manufacture |
EP1167336A2 (en) * | 2000-06-27 | 2002-01-02 | Mitsubishi Gas Chemical Company, Inc. | Process for recovering catalyst components from a mother liquor of liquid phase oxidation |
WO2006009571A1 (en) * | 2004-06-23 | 2006-01-26 | Eastman Chemical Company | Process for removal of impurities from mother liquor in the synthesis of carboxylic acid using pressure filtration |
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US5693856A (en) * | 1996-01-16 | 1997-12-02 | The Boc Group, Inc. | Production of terephthalic acid |
CN101152969B (en) * | 2006-09-29 | 2011-01-19 | 中国石油化工股份有限公司石油化工科学研究院 | Method of processing p-benzene dicarboxylic acid production wastewater |
CN101134628A (en) * | 2007-07-31 | 2008-03-05 | 凯能高科技工程(上海)有限公司 | Comprehensive processing utilization method for PTA refining waste-water |
-
2009
- 2009-08-26 CN CN2009801337289A patent/CN102137707B/en not_active Expired - Fee Related
- 2009-08-26 WO PCT/IN2009/000468 patent/WO2010032263A2/en active Application Filing
- 2009-08-26 PT PT2009000468A patent/PT2010032263W/en unknown
- 2009-08-26 BR BRPI0918260 patent/BRPI0918260B1/en not_active IP Right Cessation
- 2009-08-26 PL PL395933A patent/PL217166B1/en unknown
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
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US3170768A (en) * | 1959-04-22 | 1965-02-23 | Standard Oil Co | System for continuous preparation of terephthalic acid |
GB1460941A (en) * | 1973-03-30 | 1977-01-06 | Matsuyama Petrochemicals Inc | Method of recovering cobalt and or manganese-bromine liquid- phase oxidation catalyst |
WO1985002353A1 (en) * | 1983-11-30 | 1985-06-06 | Ecolochem, Inc. | Recovery of organic acids, catalysts and water from terephthalic acid manufacture |
EP1167336A2 (en) * | 2000-06-27 | 2002-01-02 | Mitsubishi Gas Chemical Company, Inc. | Process for recovering catalyst components from a mother liquor of liquid phase oxidation |
WO2006009571A1 (en) * | 2004-06-23 | 2006-01-26 | Eastman Chemical Company | Process for removal of impurities from mother liquor in the synthesis of carboxylic acid using pressure filtration |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102381964A (en) * | 2010-09-01 | 2012-03-21 | 天华化工机械及自动化研究设计院 | Integral process for washing and filtering terephthalic acid and water recovery |
WO2015022493A1 (en) * | 2013-08-14 | 2015-02-19 | Johnson Matthey Davy Technologies Limited | Process for recovering water, metal and organics from the production of polycarboxylic acid |
US9505698B2 (en) | 2013-08-14 | 2016-11-29 | Johnson Matthey Davy Technologies Limited | Process for recovering water, metal and organics from the production of polycarboxylic acid |
EA030560B1 (en) * | 2013-08-14 | 2018-08-31 | Джонсон Мэтти Дэйви Текнолоджис Лимитед | Process for recovering water, metal and organics from the production of polycarboxylic acid |
US9776943B2 (en) | 2014-02-20 | 2017-10-03 | Reliance Industries Limited | Catalyst recovery and recycling process during aromatic carboxylic acid production |
WO2016005920A3 (en) * | 2014-07-09 | 2016-03-10 | Reliance Industries Limited | Method for recovery of ionic liquid and system thereof |
Also Published As
Publication number | Publication date |
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WO2010032263A3 (en) | 2010-09-16 |
BRPI0918260B1 (en) | 2019-12-03 |
PL395933A1 (en) | 2011-12-05 |
BRPI0918260A2 (en) | 2015-12-15 |
PT2010032263W (en) | 2011-09-14 |
CN102137707B (en) | 2013-08-21 |
PL217166B1 (en) | 2014-06-30 |
CN102137707A (en) | 2011-07-27 |
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