US20060046217A1 - Waste treatment system for PTA and PET manufacturing plants - Google Patents

Waste treatment system for PTA and PET manufacturing plants Download PDF

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Publication number
US20060046217A1
US20060046217A1 US11/132,901 US13290105A US2006046217A1 US 20060046217 A1 US20060046217 A1 US 20060046217A1 US 13290105 A US13290105 A US 13290105A US 2006046217 A1 US2006046217 A1 US 2006046217A1
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waste
waste byproduct
byproduct stream
stream
fuel
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US11/132,901
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Joseph Parker
Timothy Upshaw
Robert Lin
Bruce DeBruin
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Eastman Chemical Co
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Eastman Chemical Co
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Priority to US11/132,901 priority Critical patent/US20060046217A1/en
Assigned to EASTMAN CHEMICAL COMPANY reassignment EASTMAN CHEMICAL COMPANY ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: DEBRUIN, BRUCE ROGER, LIN, ROBERT, PARKER, JOSEPH LUTHER, UPSHAW, TIMOTHY ALAN
Publication of US20060046217A1 publication Critical patent/US20060046217A1/en
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    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F23COMBUSTION APPARATUS; COMBUSTION PROCESSES
    • F23GCREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
    • F23G7/00Incinerators or other apparatus for consuming industrial waste, e.g. chemicals
    • F23G7/06Incinerators or other apparatus for consuming industrial waste, e.g. chemicals of waste gases or noxious gases, e.g. exhaust gases
    • F23G7/061Incinerators or other apparatus for consuming industrial waste, e.g. chemicals of waste gases or noxious gases, e.g. exhaust gases with supplementary heating
    • F23G7/065Incinerators or other apparatus for consuming industrial waste, e.g. chemicals of waste gases or noxious gases, e.g. exhaust gases with supplementary heating using gaseous or liquid fuel
    • F23G7/066Incinerators or other apparatus for consuming industrial waste, e.g. chemicals of waste gases or noxious gases, e.g. exhaust gases with supplementary heating using gaseous or liquid fuel preheating the waste gas by the heat of the combustion, e.g. recuperation type incinerator
    • F23G7/068Incinerators or other apparatus for consuming industrial waste, e.g. chemicals of waste gases or noxious gases, e.g. exhaust gases with supplementary heating using gaseous or liquid fuel preheating the waste gas by the heat of the combustion, e.g. recuperation type incinerator using regenerative heat recovery means
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F23COMBUSTION APPARATUS; COMBUSTION PROCESSES
    • F23GCREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
    • F23G5/00Incineration of waste; Incinerator constructions; Details, accessories or control therefor
    • F23G5/006General arrangement of incineration plant, e.g. flow sheets
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F23COMBUSTION APPARATUS; COMBUSTION PROCESSES
    • F23GCREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
    • F23G5/00Incineration of waste; Incinerator constructions; Details, accessories or control therefor
    • F23G5/30Incineration of waste; Incinerator constructions; Details, accessories or control therefor having a fluidised bed
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F23COMBUSTION APPARATUS; COMBUSTION PROCESSES
    • F23GCREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
    • F23G7/00Incinerators or other apparatus for consuming industrial waste, e.g. chemicals
    • F23G7/12Incinerators or other apparatus for consuming industrial waste, e.g. chemicals of plastics, e.g. rubber
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F23COMBUSTION APPARATUS; COMBUSTION PROCESSES
    • F23GCREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
    • F23G2201/00Pretreatment
    • F23G2201/70Blending
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F23COMBUSTION APPARATUS; COMBUSTION PROCESSES
    • F23GCREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
    • F23G2900/00Special features of, or arrangements for incinerators
    • F23G2900/50001Combination of two or more furnaces

Definitions

  • the present invention relates to methods and apparatus for treating the wastes produced in a polyester-manufacturing plant; and in particular, the present invention relates to methods and apparatus for treating the wastes from a PTA or PET plant in which at least one heat source utilizes fuel as a combustion source.
  • Polyester is a widely used polymeric resin used in a number of packaging and fiber based applications.
  • Poly(ethylene terephthalate) (“PET”) or a modified PET is the polymer of choice for making beverage and food containers such as plastic bottles and jars used for carbonated beverages, water, juices, foods, detergents, cosmetics, and other products. These containers are manufactured by a process that typically comprises drying the PET resin, injection molding a preform and, finally, stretch blow molding the finished bottle.
  • PET has become a commodity polymer.
  • PET is also used in a number of film and fiber applications. Commercial production of PET is energy intensive, and therefore even relatively small improvements in energy consumption are of considerable commercial value.
  • a diol such as ethylene glycol is reacted with a dicarboxylic acid or a dicarboxylic acid ester.
  • terephthalic acid is usually slurried in ethylene glycol and heated to produce a mixture of oligomers of a low degree of polymerization.
  • the reaction can be accelerated by the addition of a suitable reaction catalyst. Since the product of these condensation reaction tends to be reversible and in order to increase the molecular weight of the polyesters, this reaction is often carried out in a multi-chamber polycondensation reaction system having several reaction chambers operating in series.
  • the diol and the dicarboxylic acid component are introduced in the first reactor at a relatively high pressure. After polymerizing at an elevated temperature the resulting polymer is then transferred to the second reaction chamber which is operated at a lower pressure than the first chamber. The polymer continues to grow in this second chamber with volatile compounds being removed. This process is repeated successively for each reactor, each of which are operated at lower and lower pressures. The result of this step wise condensation is the formation of polyester with high molecular weight and higher inherent viscosity. During this polycondensation process, various additives such as colorants and UV inhibitors may be also added.
  • Polycondensation occurs at relatively high temperature, generally in the range of 280-300° C., under vacuum with water and ethylene glycol produced by the condensation being removed.
  • the heat for the polycondensation reactions is typically supplied by one or more furnaces, such as heat transfer medium furnace (“HTM furnace”).
  • HTM furnace heat transfer medium furnace
  • the waste products needing treatment in the typical PET process are acetic acid, various acid aldehydes, and unreacted ethylene glycol.
  • crude terephthalic acid is made by catalytic oxidation of para-xylene followed by purification of the crude acid.
  • Crude terephthalic acid suitable for making polyesters is typically produced by the oxidation of para-xylene in the presence of catalyst and acetic acid solvent. Oxygen in the air functions as the oxidant and converts the para-xylene in TPA.
  • the reaction mixture typically includes other components in addition to para-xylene. Such additional components include a solvent, a catalyst system, and a promoter. Suitable solvents include monocarboxylic acids such as acetic acid.
  • Catalyst systems that may be used often include a heavy metal or mixture of heavy metals such as cobalt and manganese in the form of acetate salts.
  • Bromine in the form of bromic acid is a commonly used promoter.
  • U.S. Pat. No. 6,137,001 discloses a liquid-phase process in which a benzene derivative or naphthalene derivative is oxidized with oxygen to form a carboxylic acid.
  • the reaction mixture in this process typically includes a reaction catalyst comprising a heavy metal component and a bromine source.
  • U.S. Pat. No. 5,696,285 discloses a process in which the oxidation of para-xylene is carried out using pure or nearly pure oxygen (great to or equal than 75 vol. % oxygen).
  • U.S. Pat. No. 5,420,316 discloses a process with very low amounts of aldehyde and ketone by-products in which a carboxylic acid is made by the ozonization of an organic compound having at least one olefinic bond followed by further oxidation with molecular oxygen.
  • a carboxylic acid is made by the ozonization of an organic compound having at least one olefinic bond followed by further oxidation with molecular oxygen.
  • purification by hydrogenation or other methods and crystallization can be done in order to obtain suitable material for most PET applications.
  • the main impurity (4-carboxybenzaldehyde) is transformed to water-soluble para-toluic acid during hydrogenation. It will also be appreciated that the production of TPA and PTA both produce a number of byproducts that need consideration for proper treatment and disposal.
  • the present invention overcomes one or more problems of the prior art by providing in one embodiment a method of treating waste in a polyester-manufacturing plant.
  • the method of the invention comprises combining the fuel with a first waste byproduct stream to form a combined fuel and first waste byproduct stream mixture.
  • the combined fuel and first waste byproduct mixture is introduced into the first heat source and combusted.
  • the present invention also provides certain useful variations of this method in which one or more of the following steps are performed: a second waste byproduct stream is introduced and treated in a regenerative thermal oxidizer, a third waste byproduct stream is introduced and treated in a waste water treatment plant, or a fourth waste byproduct stream is introduced and treated in a fluid bed incinerator.
  • a second method of treating waste in a polyester-manufacturing plant comprises combining the fuel with a first waste byproduct stream to form a combined fuel and first waste byproduct stream mixture.
  • the combined fuel and first waste byproduct mixture is introduced into the first heat source and combusted.
  • the method further comprises introducing a second waste byproduct stream into a regenerative thermal oxidizer and introducing a third waste byproduct stream into a fluid bed incinerator.
  • an apparatus for treating waste from a polyester-manufacturing plant that utilizes the methods of the invention.
  • the apparatus of the invention comprises a heat source that is used to both provide heat to the one or more polymerization reactors and to combust the waste and a first conduit that transfers a first waste stream from the one or more polymerization reactors to the heat source.
  • the apparatus further includes one or more of the following components: a regenerative thermal oxidizer; a waste water treatment plant; and a fluid bed incinerator.
  • FIG. 1 is a schematic illustrating embodiments of the invention that are useful for treating the waste products from PET and PTA manufacturing processes using the HTM furnace of the PET process.
  • a method of treating waste in a polyester-manufacturing plant is provided.
  • the polyester manufacturing plant 10 include PTA manufacturing component 12 and PET manufacturing component 14 .
  • PTA manufacturing component 12 produces waste byproduct streams 16 , 18 , 20 , 22 .
  • Waste byproduct stream 16 is the off-gas waste from acetic acid/water separation unit 24 which removes byproduct acetic acid from PTA manufacturing line 26 while waste byproduct stream 18 comprises the aqueous wastes from acetic acid/water separation unit 24 .
  • Waste byproduct stream 20 contains solid wastes from PTA manufacturing line 26 and waste stream 22 comprises other aqueous wastes coming directly from PTA manufacturing line 26 .
  • PET manufacturing component 14 produces waste byproduct streams 28 , 30 .
  • at least one heat source 32 is used to provide heat for the condensation reactions between the glycol and diacid that occur in at least one condensation reactor 34 .
  • Ethylene glycol/water separation unit 36 removal waste from condensation reactor 34 .
  • Waste byproduct stream 28 includes the aqueous wastes from separation unit 36 .
  • waste byproduct stream 30 includes waste from condensation reactor 34 .
  • the method of the present invention advantageously utilizes a heat from heat source 32 to combust at least one waste byproduct stream of waste byproduct streams 16 , 18 , 20 , 22 , 28 , 30 .
  • the typical polyester-manufacturing process produces a number of different waste byproducts that may be present in the first waste byproduct stream.
  • One type of waste byproduct stream comprises an aqueous waste stream which includes one or more combustible organic compounds.
  • the type of organic compounds present will depend on the specific polyester process. For example, the manufacturing of PTA or PET typically produce ethylene glycol, acetic acid, acid aldehydes, and combinations thereof.
  • the first waste byproduct stream may also include solid organic components. These solid organic components are also usually sufficiently combustible to be burned in the at least one heat source.
  • the method of the invention comprises combining fuel in conduit 40 with a first waste byproduct stream to form a combined fuel and first waste byproduct stream mixture.
  • the first waste byproduct stream is combined with the fuel via conduit 42 .
  • Such a mixing of the fuel and first waste byproduct stream may occur within heat source 32 or prior to introduction of the fuel into heat source 32 .
  • the combined fuel and first waste byproduct mixture is introduced into heat source 32 and combusted. Accordingly, at least a portion of the waste byproduct stream 30 is at least partially combusted along with the fuel.
  • heat source 32 is a heat transfer medium furnace (“HTM furnace”) in which a liquid is circulated in a coil 38 that is exposed to an open flame and then further circulated to heat exchange devices which transfer heat to polymer forming reactors.
  • HTM furnace heat transfer medium furnace
  • the open flame is formed by the combustion of the fuel in conduit 40 and first waste byproduct stream 30 .
  • coil 38 of the HTM furnace is heated to a temperature greater than about 300° C.
  • suitable fuels include natural gas, fuel oil, and combinations thereof.
  • the first waste byproduct stream will combine one or more of waste byproduct streams 16 , 18 , 20 , 22 , 28 , 30 .
  • the first waste byproduct stream combines all of waste byproducts 16 , 18 , 20 , 22 , 28 , 30 .
  • the method of the present invention further comprises introducing a second waste byproduct stream into a regenerative thermal oxidizer (“RTO”).
  • RTOs are particularly suitable for removing (oxidizing) byproduct streams that include a significant amount of vapor-phase compounds. Often, such byproduct streams will include an inert gas and one or more volatile organic compounds. Examples of volatile organic compounds that are present in the waste streams of PTA and PET plants are acetic acid, methyl acetate, and combinations thereof.
  • the second waste product stream may also be a liquid waste stream which is vaporized before the second waste byproduct stream is introduced into the regenerative thermal oxidizer.
  • the second waste byproduct stream will include the combination of one or more of waste byproduct streams 16 , 18 , 22 , 28 , 30 .
  • the first waste byproduct stream that is fed into heat source 32 includes wastes stream 20 while the second waste byproduct stream includes waste streams 16 , 18 , 22 , 28 , 30 which are fed to RTO 50 via conduit 52 .
  • the first waste byproduct stream comprises waste byproduct streams 18 , 22 , 20 , 28 , 30 and the second waste byproduct stream includes waste stream 16 .
  • the method of the invention further comprises introducing a third waste byproduct stream into a waste water treatment plant 60 via conduit 62 .
  • This second variation is performed either separately from or in combination with the second variation set forth above.
  • the third waste byproduct stream will include the combination of one or more of waste streams 18 , 22 , 28 , 30 .
  • waste stream 20 is fed to heat source 32
  • waste stream 16 is fed into RTO 50 via conduit 52
  • waste streams 18 , 22 , 28 , 30 are fed to one of heat source 32 , RTO 50 , or water treatment plant 60 .
  • the method of the invention further comprises introducing a fourth waste byproduct stream that is fed into a fluid bed incinerator 70 via conduit 72 .
  • the fourth waste byproduct stream comprises solid organic components, the solid organic components being sufficiently combustible to be burned in the at least one heat source.
  • the fourth waste byproduct stream may be the take off gas from a distillation tower from the various purification stages in a PET or PTA process.
  • this fourth waste byproduct stream may contain an aqueous waste stream which includes a combustible organic compound.
  • the fourth waste byproduct stream will comprise waste stream 20 .
  • waste stream 16 is fed into RTO 50
  • waste stream 20 is feed to fluid bed incinerator 70
  • waste streams 18 , 22 , 28 , 30 are fed to heat source 32 , RTO 50 , or water treatment plant 60 .
  • a second method of treating waste in a polyester-manufacturing plant is provided.
  • polyester-manufacturing plants typically produce one or more waste byproduct streams.
  • such plants will typically have at least one heat source utilizing fuel as a combustion source.
  • the method of this embodiment comprises combining the fuel with a first waste byproduct stream to form a combined fuel and first waste byproduct stream mixture.
  • the combined fuel and first waste byproduct mixture is introduced into heat source 32 and combusted.
  • the method further comprises introducing a second waste byproduct stream into RTO 50 via conduit 52 and introducing a third waste byproduct stream into a fluid bed incinerator 70 via conduit 72 .
  • the selection of the heat source is the same as that set forth above for the first embodiment.
  • waste stream 16 is fed to RTO 50
  • waste stream 20 is feed to fluid bed incinerator 70
  • waste streams 18 , 22 , 28 , 30 are fed to heat source 32 or RTO 50 .
  • an apparatus for treating waste from a polyester-manufacturing plant includes heat source 32 that is used to both provide heat to at least one condensation reactor 34 and to combust the waste.
  • the apparatus also includes a first conduit 42 that transfers a first waste stream from the one or more polymerization reactors to the heat source. The selection of a suitable heat source is the same as that set forth above for the methods of the invention.
  • a suitable heat source is a HTM furnace in which a liquid is circulated in a coil that is exposed to an open flame and then further circulated to heat exchange devices which transfer heat to polymer forming reactors, the open flame being formed by the combustion of the fuel and the one or more waste byproduct steams.
  • the apparatus further includes RTO 50 with or without waste water treatment plant 60 and/or fluid bed incinerator 70 .
  • the apparatus of the invention includes heat source 32 , RTO 50 , and fluid bed incinerator 70 .

Abstract

The present invention provides a method for treating the wastes of polyester-manufacturing processes. The method of the invention comprises combining the fuel with a first waste byproduct stream to form a combined fuel and first waste byproduct stream mixture that is combusted in a furnace. The present invention also provides certain useful variations of this method in which one or more of the following steps are performed: a second waste byproduct stream is introduced and treated in a regenerative thermal oxidizer, a third waste byproduct stream is introduced and treated in a waste water treatment plant, or a fourth waste byproduct stream is introduced and treated in a fluid bed incinerator. The present invention also provides an apparatus that executes the methods of the invention.

Description

    CROSS-REFERENCE TO RELATED APPLICATIONS
  • This application claims priority to U.S. Provisional Application Ser. No. 60/606,857, filed Sep. 2, 2004, the disclosure of which is incorporated herein by this reference to the extent it does not contradict statements made herein.
  • FIELD OF THE INVENTION
  • The present invention relates to methods and apparatus for treating the wastes produced in a polyester-manufacturing plant; and in particular, the present invention relates to methods and apparatus for treating the wastes from a PTA or PET plant in which at least one heat source utilizes fuel as a combustion source.
  • BACKGROUND
  • Polyester is a widely used polymeric resin used in a number of packaging and fiber based applications. Poly(ethylene terephthalate) (“PET”) or a modified PET is the polymer of choice for making beverage and food containers such as plastic bottles and jars used for carbonated beverages, water, juices, foods, detergents, cosmetics, and other products. These containers are manufactured by a process that typically comprises drying the PET resin, injection molding a preform and, finally, stretch blow molding the finished bottle. Despite the stringent matrix of properties required for such uses, particularly for food packaging, PET has become a commodity polymer. PET is also used in a number of film and fiber applications. Commercial production of PET is energy intensive, and therefore even relatively small improvements in energy consumption are of considerable commercial value.
  • In the typical polyester forming polycondensation reaction, a diol such as ethylene glycol is reacted with a dicarboxylic acid or a dicarboxylic acid ester. In the production of PET, terephthalic acid is usually slurried in ethylene glycol and heated to produce a mixture of oligomers of a low degree of polymerization. The reaction can be accelerated by the addition of a suitable reaction catalyst. Since the product of these condensation reaction tends to be reversible and in order to increase the molecular weight of the polyesters, this reaction is often carried out in a multi-chamber polycondensation reaction system having several reaction chambers operating in series. Typically, the diol and the dicarboxylic acid component are introduced in the first reactor at a relatively high pressure. After polymerizing at an elevated temperature the resulting polymer is then transferred to the second reaction chamber which is operated at a lower pressure than the first chamber. The polymer continues to grow in this second chamber with volatile compounds being removed. This process is repeated successively for each reactor, each of which are operated at lower and lower pressures. The result of this step wise condensation is the formation of polyester with high molecular weight and higher inherent viscosity. During this polycondensation process, various additives such as colorants and UV inhibitors may be also added. Polycondensation occurs at relatively high temperature, generally in the range of 280-300° C., under vacuum with water and ethylene glycol produced by the condensation being removed. The heat for the polycondensation reactions is typically supplied by one or more furnaces, such as heat transfer medium furnace (“HTM furnace”). Moreover, the during the polycondensation process, a number of chemical waste byproducts are formed that need to be appropriately treated in order to meet government regulations. Among the waste products needing treatment in the typical PET process are acetic acid, various acid aldehydes, and unreacted ethylene glycol.
  • In the typical process for making purified terephthalic acid (“PTA”), crude terephthalic acid is made by catalytic oxidation of para-xylene followed by purification of the crude acid. Crude terephthalic acid suitable for making polyesters is typically produced by the oxidation of para-xylene in the presence of catalyst and acetic acid solvent. Oxygen in the air functions as the oxidant and converts the para-xylene in TPA. The reaction mixture typically includes other components in addition to para-xylene. Such additional components include a solvent, a catalyst system, and a promoter. Suitable solvents include monocarboxylic acids such as acetic acid. Catalyst systems that may be used often include a heavy metal or mixture of heavy metals such as cobalt and manganese in the form of acetate salts. Bromine in the form of bromic acid is a commonly used promoter. For example, U.S. Pat. No. 6,137,001 discloses a liquid-phase process in which a benzene derivative or naphthalene derivative is oxidized with oxygen to form a carboxylic acid. The reaction mixture in this process typically includes a reaction catalyst comprising a heavy metal component and a bromine source. U.S. Pat. No. 5,696,285 discloses a process in which the oxidation of para-xylene is carried out using pure or nearly pure oxygen (great to or equal than 75 vol. % oxygen). This process also improves reaction efficiency by rapid dilution of the hydrocarbon feed stock. In a somewhat similar process, U.S. Pat. No. 5,420,316 discloses a process with very low amounts of aldehyde and ketone by-products in which a carboxylic acid is made by the ozonization of an organic compound having at least one olefinic bond followed by further oxidation with molecular oxygen. After manufacturing of the crude terephthalic acid, purification by hydrogenation or other methods and crystallization can be done in order to obtain suitable material for most PET applications. The main impurity (4-carboxybenzaldehyde) is transformed to water-soluble para-toluic acid during hydrogenation. It will also be appreciated that the production of TPA and PTA both produce a number of byproducts that need consideration for proper treatment and disposal.
  • Accordingly, there is a need for improved methods and apparatus for treating the waste byproducts formed in the various polyester-manufacturing processes in an energy efficient manner.
  • SUMMARY OF THE INVENTION
  • The present invention overcomes one or more problems of the prior art by providing in one embodiment a method of treating waste in a polyester-manufacturing plant. The method of the invention comprises combining the fuel with a first waste byproduct stream to form a combined fuel and first waste byproduct stream mixture. Next, the combined fuel and first waste byproduct mixture is introduced into the first heat source and combusted. The present invention also provides certain useful variations of this method in which one or more of the following steps are performed: a second waste byproduct stream is introduced and treated in a regenerative thermal oxidizer, a third waste byproduct stream is introduced and treated in a waste water treatment plant, or a fourth waste byproduct stream is introduced and treated in a fluid bed incinerator.
  • In another embodiment of the invention, a second method of treating waste in a polyester-manufacturing plant is provided. The method of this embodiment comprises combining the fuel with a first waste byproduct stream to form a combined fuel and first waste byproduct stream mixture. Next, the combined fuel and first waste byproduct mixture is introduced into the first heat source and combusted. The method further comprises introducing a second waste byproduct stream into a regenerative thermal oxidizer and introducing a third waste byproduct stream into a fluid bed incinerator.
  • In yet another embodiment of the invention, an apparatus for treating waste from a polyester-manufacturing plant that utilizes the methods of the invention is provided. The apparatus of the invention comprises a heat source that is used to both provide heat to the one or more polymerization reactors and to combust the waste and a first conduit that transfers a first waste stream from the one or more polymerization reactors to the heat source. In certain variations of the apparatus of the invention, the apparatus further includes one or more of the following components: a regenerative thermal oxidizer; a waste water treatment plant; and a fluid bed incinerator.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 is a schematic illustrating embodiments of the invention that are useful for treating the waste products from PET and PTA manufacturing processes using the HTM furnace of the PET process.
  • DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT(S)
  • Reference will now be made in detail to presently preferred compositions or embodiments and methods of the invention, which constitute the best modes of practicing the invention presently known to the inventor.
  • In an embodiment of the present invention, a method of treating waste in a polyester-manufacturing plant is provided. With reference to FIG. 1, a schematic of a polyester-manufacturing plant in which PTA and PET are both formed is provided. The polyester manufacturing plant 10 include PTA manufacturing component 12 and PET manufacturing component 14. PTA manufacturing component 12 produces waste byproduct streams 16, 18, 20, 22. Waste byproduct stream 16 is the off-gas waste from acetic acid/water separation unit 24 which removes byproduct acetic acid from PTA manufacturing line 26 while waste byproduct stream 18 comprises the aqueous wastes from acetic acid/water separation unit 24. Waste byproduct stream 20 contains solid wastes from PTA manufacturing line 26 and waste stream 22 comprises other aqueous wastes coming directly from PTA manufacturing line 26.
  • PET manufacturing component 14 produces waste byproduct streams 28, 30. In PET manufacturing component 14, at least one heat source 32 is used to provide heat for the condensation reactions between the glycol and diacid that occur in at least one condensation reactor 34. Ethylene glycol/water separation unit 36 removal waste from condensation reactor 34. Waste byproduct stream 28 includes the aqueous wastes from separation unit 36. Similarly, waste byproduct stream 30 includes waste from condensation reactor 34. As will be shown below, the method of the present invention advantageously utilizes a heat from heat source 32 to combust at least one waste byproduct stream of waste byproduct streams 16, 18, 20, 22, 28, 30. The typical polyester-manufacturing process produces a number of different waste byproducts that may be present in the first waste byproduct stream. One type of waste byproduct stream comprises an aqueous waste stream which includes one or more combustible organic compounds. The type of organic compounds present will depend on the specific polyester process. For example, the manufacturing of PTA or PET typically produce ethylene glycol, acetic acid, acid aldehydes, and combinations thereof. In addition to the aqueous waste streams, the first waste byproduct stream may also include solid organic components. These solid organic components are also usually sufficiently combustible to be burned in the at least one heat source.
  • Still referring to FIG. 1, the method of the invention comprises combining fuel in conduit 40 with a first waste byproduct stream to form a combined fuel and first waste byproduct stream mixture. The first waste byproduct stream is combined with the fuel via conduit 42. Such a mixing of the fuel and first waste byproduct stream may occur within heat source 32 or prior to introduction of the fuel into heat source 32. The combined fuel and first waste byproduct mixture is introduced into heat source 32 and combusted. Accordingly, at least a portion of the waste byproduct stream 30 is at least partially combusted along with the fuel. Typically, heat source 32 is a heat transfer medium furnace (“HTM furnace”) in which a liquid is circulated in a coil 38 that is exposed to an open flame and then further circulated to heat exchange devices which transfer heat to polymer forming reactors. As used in the present embodiment, the open flame is formed by the combustion of the fuel in conduit 40 and first waste byproduct stream 30. Usually, coil 38 of the HTM furnace is heated to a temperature greater than about 300° C. A variety of fuels may be used in heat source 32. Examples of suitable fuels include natural gas, fuel oil, and combinations thereof.
  • In a first variation of the invention, the first waste byproduct stream will combine one or more of waste byproduct streams 16, 18, 20, 22, 28, 30. Preferably, the first waste byproduct stream combines all of waste byproducts 16, 18, 20, 22, 28, 30.
  • In a second variation of the present embodiment, the method of the present invention further comprises introducing a second waste byproduct stream into a regenerative thermal oxidizer (“RTO”). RTOs are particularly suitable for removing (oxidizing) byproduct streams that include a significant amount of vapor-phase compounds. Often, such byproduct streams will include an inert gas and one or more volatile organic compounds. Examples of volatile organic compounds that are present in the waste streams of PTA and PET plants are acetic acid, methyl acetate, and combinations thereof. The second waste product stream may also be a liquid waste stream which is vaporized before the second waste byproduct stream is introduced into the regenerative thermal oxidizer. In accordance with this variation, the second waste byproduct stream will include the combination of one or more of waste byproduct streams 16, 18, 22, 28, 30. For example, the first waste byproduct stream that is fed into heat source 32 includes wastes stream 20 while the second waste byproduct stream includes waste streams 16, 18, 22, 28, 30 which are fed to RTO 50 via conduit 52. Alternatively, for example, the first waste byproduct stream comprises waste byproduct streams 18, 22, 20, 28, 30 and the second waste byproduct stream includes waste stream 16.
  • In a third variation of the present embodiment, the method of the invention further comprises introducing a third waste byproduct stream into a waste water treatment plant 60 via conduit 62. This second variation is performed either separately from or in combination with the second variation set forth above. In accordance with this variation, the third waste byproduct stream will include the combination of one or more of waste streams 18, 22, 28, 30. For example, waste stream 20 is fed to heat source 32, waste stream 16 is fed into RTO 50 via conduit 52, and waste streams 18, 22, 28, 30 are fed to one of heat source 32, RTO 50, or water treatment plant 60.
  • In a fourth variation of the present embodiment, the method of the invention further comprises introducing a fourth waste byproduct stream that is fed into a fluid bed incinerator 70 via conduit 72. Again, this variation is performed separately from or in combination with the first, second, and third variations. The fourth waste byproduct stream comprises solid organic components, the solid organic components being sufficiently combustible to be burned in the at least one heat source. Moreover, the fourth waste byproduct stream may be the take off gas from a distillation tower from the various purification stages in a PET or PTA process. Furthermore, this fourth waste byproduct stream may contain an aqueous waste stream which includes a combustible organic compound. As set forth above, examples of combustible organic compounds that are present in a PET or PTA plant are ethylene glycol, acetic acid, acid aldehydes, and combinations thereof. In accordance with this variation, the fourth waste byproduct stream will comprise waste stream 20. For example, waste stream 16 is fed into RTO 50, waste stream 20 is feed to fluid bed incinerator 70, and waste streams 18, 22, 28, 30 are fed to heat source 32, RTO 50, or water treatment plant 60.
  • In another embodiment of the invention, a second method of treating waste in a polyester-manufacturing plant is provided. As set forth above, polyester-manufacturing plants typically produce one or more waste byproduct streams. Moreover, such plants will typically have at least one heat source utilizing fuel as a combustion source. The method of this embodiment comprises combining the fuel with a first waste byproduct stream to form a combined fuel and first waste byproduct stream mixture. Next, the combined fuel and first waste byproduct mixture is introduced into heat source 32 and combusted. The method further comprises introducing a second waste byproduct stream into RTO 50 via conduit 52 and introducing a third waste byproduct stream into a fluid bed incinerator 70 via conduit 72. The selection of the heat source is the same as that set forth above for the first embodiment. Moreover, the selection of the compositions of the first waste byproduct stream, the second waste by byproduct stream, and the third waste byproduct streams are also the same as those set forth above. For example waste stream 16 is fed to RTO 50, waste stream 20 is feed to fluid bed incinerator 70, and waste streams 18, 22, 28, 30 are fed to heat source 32 or RTO 50.
  • In yet another embodiment of the invention, an apparatus for treating waste from a polyester-manufacturing plant is provided. With reference to FIG. 1, the apparatus of the invention include heat source 32 that is used to both provide heat to at least one condensation reactor 34 and to combust the waste. The apparatus also includes a first conduit 42 that transfers a first waste stream from the one or more polymerization reactors to the heat source. The selection of a suitable heat source is the same as that set forth above for the methods of the invention. Specifically, a suitable heat source is a HTM furnace in which a liquid is circulated in a coil that is exposed to an open flame and then further circulated to heat exchange devices which transfer heat to polymer forming reactors, the open flame being formed by the combustion of the fuel and the one or more waste byproduct steams. In a first variation of the apparatus of the invention, the apparatus further includes RTO 50 with or without waste water treatment plant 60 and/or fluid bed incinerator 70. In a second variation, the apparatus of the invention includes heat source 32, RTO 50, and fluid bed incinerator 70.
  • While embodiments of the invention have been illustrated and described, it is not intended that these embodiments illustrate and describe all possible forms of the invention. Rather, the words used in the specification are words of description rather than limitation, and it is understood that various changes may be made without departing from the spirit and scope of the invention.

Claims (30)

1. A method of treating waste in a polyester-manufacturing plant, the polyester-manufacturing plant producing one or more waste byproduct streams and having at least one heat source utilizing a fuel as a combustion source, the method comprising:
combining the fuel with a first waste byproduct stream to form a combined fuel and first waste byproduct mixture; and
combusting the combined fuel and first waste byproduct mixture in the at least one heat source; and
wherein the second waste byproduct stream is a liquid waste stream which is vaporized before the second waste byproduct stream is introduced into the regenerative thermal oxidizer.
2. The method of claim 1 wherein the at least one heat source is a heat transfer medium furnace in which a liquid is circulated in a coil that is exposed to an open flame and then further circulated to heat exchange devices which transfer heat to polymer forming reactors, the open flame being formed by the combustion of the fuel and the one or more waste byproduct steams.
3. The method of claim 2 wherein the coil is heated to a temperature of greater than about 300° C.
4. The method of claim 2 wherein the fuel comprising a component selected from the group consisting of natural gas, fuel oil, or combinations thereof.
5. The method of claim 1 wherein the first waste byproduct stream comprises an aqueous waste stream which includes an organic compound.
6. The method of claim 5 wherein the combustible organic compound is selected from the group consisting of ethylene glycol, acetic acid, acid aldehydes, and combinations thereof.
7. The method of claim 1 wherein the polyester-manufacturing plant is a PET or PTA forming plant.
8. The method of claim 1 wherein the first waste byproduct stream comprises solid organic components, the solid organic components being sufficiently combustible to be burned in the at least one heat source.
9. The method of claim 1 wherein the polyester-manufacturing plant comprises one or more reactors in which polycondensation is utilized to form a polyester.
10. The method of claim 1 further comprising introducing a second waste byproduct stream into a regenerative thermal oxidizer.
11. The method of claim 10 wherein the second waste byproduct stream comprises a significant amount of non-condensble compounds.
12. The method of claim 11 wherein the second waste byproduct stream comprises an inert gas and a volatile organic compound.
13. The method of claim 12 wherein the volatile organic compound is selected from the group consisting of acetic acid, methyl acetate, and combinations thereof.
14. The method of claim 10 wherein the second waste byproduct stream is a liquid waste stream which is vaporized before the second waste byproduct stream is introduced into the regenerative thermal oxidizer.
15. The method of claim 10 further comprising introducing a third waste byproduct stream into a waste water treatment plant.
16. The method of claim 15 further comprising introducing a fourth waste byproduct stream into a fluid bed incinerator.
17. The method of claim 16 wherein the fourth waste byproduct stream comprises solid organic components, the solid organic components being sufficiently combustible to be burned in the at least one heat source.
18. The method of claim 17 wherein the fourth waste byproduct stream comprise the take off gas from a distillation tower.
19. The method of claim 18 wherein the fourth waste byproduct stream comprises an aqueous waste stream which includes a volatile organic compound.
20. The method of claim 19 wherein the combustible organic compound is selected from the group consisting of ethylene glycol, acetic acid, acid aldehydes, and combinations thereof.
21. A method of treating waste in a polyester-manufacturing plant, the polyester forming plant producing one or more waste byproduct streams and having at least one heat source utilizing a fuel as a combustion source, the method comprising:
combining the fuel with a first waste byproduct stream such that at least a portion of the waste byproduct stream is at least partially combusted with the fuel;
introducing a second waste byproduct stream into a regenerative thermal oxidizer; and
introducing a third waste byproduct stream into a fluid bed incinerator; and
wherein the second waste byproduct stream is a liquid waste stream which is vaporized before the second waste byproduct stream is introduced into the regenerative thermal oxidizer.
22. The method of claim 21 wherein the at least one heat source is a heat transfer medium furnace in which a liquid is circulated in a coil that is exposed to an open flame and then further circulated to heat exchange devices which transfer heat to polymer forming reactors, the open flame being formed by the combustion of the fuel and the one or more waste byproduct steams.
23. The method of claim 21 wherein the second waste byproduct stream comprises a significant amount of non-condensible compounds.
24. The method of claim 21 wherein the second waste byproduct stream comprises an inert gas and a volatile organic compound.
25. The method of claim 24 wherein the volatile organic compound is selected from the group consisting of acetic acid, methyl acetate, and combinations thereof.
26. The method of claim 21 wherein the second waste byproduct stream is a liquid waste stream which is vaporized before the second waste byproduct stream is introduced into the regenerative thermal oxidizer.
27. The method of claim 26 wherein the third waste byproduct stream comprises solid organic components, the solid organic components being sufficiently combustible to be burned in the at least one heat source.
28. The method of claim 26 wherein the third waste byproduct stream comprise the take off gas from a distillation tower.
29. The method of claim 28 wherein the third waste byproduct stream comprises an aqueous waste stream which includes a volatile organic compound.
30. The method of claim 29 wherein the combustible organic compound is selected from the group consisting of ethylene glycol, acetic acid, acid aldehydes, and combinations thereof.
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Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20080179247A1 (en) * 2007-01-30 2008-07-31 Eastman Chemical Company Elimination of Wastewater Treatment System
US20100113824A1 (en) * 2008-10-31 2010-05-06 Eastman Chemical Company Dicarboxylic Acid Production with Self-Fuel Oxidative Destruction
RU2538488C2 (en) * 2008-10-31 2015-01-10 Групо Петротемекс, С.А. Де С.В. Obtaining dicarboxylic acids with increased energy regeneration
RU2575118C2 (en) * 2008-10-31 2016-02-10 Групо Петротемекс, С.А. Де С.В. Obtaining dicarboxylic acid by method of self-activated oxidative destruction
RU2575927C2 (en) * 2008-10-31 2016-02-27 Групо Петротемекс, С.А. Де С.В. Production of dicarboxylic acid with minimal formation of sewage waters
RU2577244C2 (en) * 2008-10-31 2016-03-10 Групо Петротемекс, С.А. Де С.В. Obtaining dicarboxylic acid with direct heating of off-gas with flame
CN110805913A (en) * 2019-11-11 2020-02-18 江苏华旭环保股份有限公司 Process for producing cobalt manganese oxide by using PTA (pure terephthalic acid) activated sludge and benzoic acid rectification residues
CN110805914A (en) * 2019-11-11 2020-02-18 江苏华旭环保股份有限公司 Rotary kiln drying incineration process for PTA activated sludge with additional pre-dryer
US20210262659A1 (en) * 2018-06-12 2021-08-26 General Electric Company System and method for processing an exhaust gas

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3934969A (en) * 1973-12-22 1976-01-27 Kawasaki Jukogyo Kabushiki Kaisha Method for burning emulsion oils
US5245937A (en) * 1989-05-29 1993-09-21 Mitsui Engineering & Shipbuilding Co., Ltd. Method and apparatus for burning combustible solid residue from chemical plant
US5420316A (en) * 1994-02-10 1995-05-30 Henkel Corporation Process for making carboxylic acids
US5464540A (en) * 1993-12-09 1995-11-07 Bend Research, Inc. Pervaporation by countercurrent condensable sweep
US5696285A (en) * 1995-12-29 1997-12-09 Praxair Technology, Inc. Production of terephthalic acid with excellent optical properties through the use of pure or nearly pure oxygen as the oxidant in p-xylene oxidation
US5771821A (en) * 1994-03-25 1998-06-30 Science-Technical And Product-Innovative Center "Tokema" Method of treating plastic waste
US6137001A (en) * 1998-02-11 2000-10-24 Bp Amoco Corporation Process for preparing aromatic carboxylic acids with efficient treatments of gaseous effluent
US6703479B1 (en) * 2001-12-03 2004-03-09 Uop Llc Process and apparatus for cooling polymer in a reactor
US6964729B1 (en) * 2000-09-05 2005-11-15 Parviz Khosrowyar Oxidizing undesired compounds resident within liquid absorbent compounds, reducing atmospheric pollution, regenerating a liquid absorbent and conserving fuel usage associated with reboiler utilization

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3934969A (en) * 1973-12-22 1976-01-27 Kawasaki Jukogyo Kabushiki Kaisha Method for burning emulsion oils
US5245937A (en) * 1989-05-29 1993-09-21 Mitsui Engineering & Shipbuilding Co., Ltd. Method and apparatus for burning combustible solid residue from chemical plant
US5464540A (en) * 1993-12-09 1995-11-07 Bend Research, Inc. Pervaporation by countercurrent condensable sweep
US5420316A (en) * 1994-02-10 1995-05-30 Henkel Corporation Process for making carboxylic acids
US5771821A (en) * 1994-03-25 1998-06-30 Science-Technical And Product-Innovative Center "Tokema" Method of treating plastic waste
US5696285A (en) * 1995-12-29 1997-12-09 Praxair Technology, Inc. Production of terephthalic acid with excellent optical properties through the use of pure or nearly pure oxygen as the oxidant in p-xylene oxidation
US6137001A (en) * 1998-02-11 2000-10-24 Bp Amoco Corporation Process for preparing aromatic carboxylic acids with efficient treatments of gaseous effluent
US6964729B1 (en) * 2000-09-05 2005-11-15 Parviz Khosrowyar Oxidizing undesired compounds resident within liquid absorbent compounds, reducing atmospheric pollution, regenerating a liquid absorbent and conserving fuel usage associated with reboiler utilization
US6703479B1 (en) * 2001-12-03 2004-03-09 Uop Llc Process and apparatus for cooling polymer in a reactor

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20080179247A1 (en) * 2007-01-30 2008-07-31 Eastman Chemical Company Elimination of Wastewater Treatment System
US20100113824A1 (en) * 2008-10-31 2010-05-06 Eastman Chemical Company Dicarboxylic Acid Production with Self-Fuel Oxidative Destruction
RU2538488C2 (en) * 2008-10-31 2015-01-10 Групо Петротемекс, С.А. Де С.В. Obtaining dicarboxylic acids with increased energy regeneration
RU2575118C2 (en) * 2008-10-31 2016-02-10 Групо Петротемекс, С.А. Де С.В. Obtaining dicarboxylic acid by method of self-activated oxidative destruction
RU2575927C2 (en) * 2008-10-31 2016-02-27 Групо Петротемекс, С.А. Де С.В. Production of dicarboxylic acid with minimal formation of sewage waters
RU2577244C2 (en) * 2008-10-31 2016-03-10 Групо Петротемекс, С.А. Де С.В. Obtaining dicarboxylic acid with direct heating of off-gas with flame
US9505692B2 (en) * 2008-10-31 2016-11-29 Grupo Petrotemex, S.A. De C.V. Dicarboxylic acid production with self-fuel oxidative destruction
US20210262659A1 (en) * 2018-06-12 2021-08-26 General Electric Company System and method for processing an exhaust gas
CN110805913A (en) * 2019-11-11 2020-02-18 江苏华旭环保股份有限公司 Process for producing cobalt manganese oxide by using PTA (pure terephthalic acid) activated sludge and benzoic acid rectification residues
CN110805914A (en) * 2019-11-11 2020-02-18 江苏华旭环保股份有限公司 Rotary kiln drying incineration process for PTA activated sludge with additional pre-dryer

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