US20180304239A1 - Purification catalyst for interior of polymer film production furnace and purification method for interior of polymer film production furnace - Google Patents

Purification catalyst for interior of polymer film production furnace and purification method for interior of polymer film production furnace Download PDF

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US20180304239A1
US20180304239A1 US15/769,283 US201615769283A US2018304239A1 US 20180304239 A1 US20180304239 A1 US 20180304239A1 US 201615769283 A US201615769283 A US 201615769283A US 2018304239 A1 US2018304239 A1 US 2018304239A1
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catalyst
polymer film
film production
production furnace
furnace
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Toshiya Nashida
Naoki TONE
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Nikki Universal Co Ltd
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    • B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
    • B01J23/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/84—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • B01J23/889—Manganese, technetium or rhenium
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    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
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    • B01D53/34—Chemical or biological purification of waste gases
    • B01D53/74—General processes for purification of waste gases; Apparatus or devices specially adapted therefor
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    • B01D53/74—General processes for purification of waste gases; Apparatus or devices specially adapted therefor
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    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
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    • B01J23/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/84—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • B01J23/889—Manganese, technetium or rhenium
    • B01J23/8892—Manganese
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    • B01J35/60—Catalysts, in general, characterised by their form or physical properties characterised by their surface properties or porosity
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    • B01J35/613—10-100 m2/g
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    • B01J35/60—Catalysts, in general, characterised by their form or physical properties characterised by their surface properties or porosity
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    • B01J35/615—100-500 m2/g
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C55/00—Shaping by stretching, e.g. drawing through a die; Apparatus therefor
    • B29C55/02—Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets
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    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/18—Manufacture of films or sheets
    • B—PERFORMING OPERATIONS; TRANSPORTING
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    • B01D2255/00—Catalysts
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    • B01D—SEPARATION
    • B01D2255/00—Catalysts
    • B01D2255/90—Physical characteristics of catalysts
    • B01D2255/92—Dimensions
    • B01D2255/9207—Specific surface
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
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    • B01D2257/70—Organic compounds not provided for in groups B01D2257/00 - B01D2257/602
    • B01D2257/708—Volatile organic compounds V.O.C.'s
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    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
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    • B01J2523/00—Constitutive chemical elements of heterogeneous catalysts
    • B01J2523/10—Constitutive chemical elements of heterogeneous catalysts of Group I (IA or IB) of the Periodic Table
    • B01J2523/13—Potassium
    • B—PERFORMING OPERATIONS; TRANSPORTING
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    • B01J2523/00—Constitutive chemical elements of heterogeneous catalysts
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    • B01J2523/00—Constitutive chemical elements of heterogeneous catalysts
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    • B01J2523/72—Manganese
    • 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
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Definitions

  • This invention relates to a catalyst for removing volatile organic compounds (VOCs) or sublimable organic substances generated in a polymer film production furnace; and a method for purifying a gas inside a polymer film production furnace with the use of the catalyst.
  • VOCs volatile organic compounds
  • VOCs volatile organic compounds
  • sublimable organic compounds, etc. derived from a starting polymer
  • Patent Literature 1 discloses the technology of passing hot air within a tenter furnace in PET film production through an oxidation catalyst layer composed of a platinum group metal (ruthenium, rhodium, palladium, osmium, iridium, or platinum).
  • a platinum group metal ruthenium, rhodium, palladium, osmium, iridium, or platinum.
  • Patent Literature 2 discloses a technology which, during production of a PET film with hot air being circulated within a tenter furnace, comprises burning and removing an oligomer generated within the tenter furnace with the use of an oxidation catalyst, and blowing the hot air after removal of the oligomer against the surface of the film.
  • Patent Literature 3 discloses a technology in a process for production of a biaxially oriented polyester film, the technology comprising arranging a platinum catalyst in a hot air circulation path, thereby subjecting low molecular weight substances, which have volatilized from the film and mixed into circulated hot air, to efficient combustion treatment with the platinum catalyst.
  • Patent Literature 4 discloses a technology using a filter incorporating a platinum catalyst block for removal of an oligomer.
  • Patent Literature 5 discloses the technology of providing a tenter with a catalyst for decomposition and removal of a sublimate which has resulted from a thermoplastic resin.
  • an oxidation catalyst is used to treat a gas inside a drafting oven in a PET stretching device; that a platinum group metal (ruthenium, rhodium, palladium, osmium, iridium, or platinum) is used as an active ingredient of the oxidation catalyst; and that the treated gas is circulated and used again.
  • a platinum group metal ruthenium, rhodium, palladium, osmium, iridium, or platinum
  • Patent Literature 6 discloses a purification catalyst for a gas inside a PET drafting oven, the purification catalyst containing at least one inorganic oxide, namely alumina or zirconium oxide, and platinum.
  • the literature also discloses that the purification catalyst may contain zeolite.
  • Patent Literature 6 describes that the following effects can be obtained by possessing the above-mentioned features: (1) A sublimable polymer contained in the gas inside the PET drafting oven, such as a PET oligomer, is oxidatively decomposed at a high conversion rate to be converted into CO 2 and H 2 O. The purification catalyst has activity minimally decreased, and is excellent in durability. (2) Aldehydes generated during PET film stretching are oxidatively decomposed at the same time. (3) Long-term purification of the gas inside the PET drafting oven, which has been difficult to achieve using so far known catalysts, can be achieved. Thus, staining of the drafting oven can be prevented, and a burden on the maintenance and administration of the drafting oven can be lessened.
  • Patent Literatures 1 to 5 do not report the details of the catalysts.
  • Silicon-containing compounds or organic sulfur compounds derived from additives incorporated in a polymer film may be included within a polymer film production furnace. Since they cause a decline in catalytic activity, the durability of the catalyst is also important. Moreover, aldehydes such as acetaldehyde are generated, so that a catalyst simultaneously decomposing and removing them is desired.
  • Patent Literature 6 shows that its purification catalyst exhibits excellent performance in removing the PET oligomer generated inside the PET furnace. However, this literature is silent on the removal of volatile organic compounds generated inside production furnaces for other polymer films.
  • VOCs volatile organic compounds
  • the present inventors developed a novel catalyst for decomposing volatile organic compounds (VOCs) or sublimable organic substances, generated inside a polymer film production furnace, at a high conversion rate. They have found that this catalyst is excellent in durability, and have accomplished the present invention.
  • the gist of the present invention is as follows:
  • a purification catalyst for a gas inside a polymer film production furnace the purification catalyst containing a mixed oxide composed of a manganese-based oxide, which contains manganese and potassium and has a cryptomelane structure, and copper oxide.
  • a method for purifying a gas inside a polymer film production furnace comprising: a step 1 of bringing hot air containing volatile and/or sublimable organic substances, generated during production of a polymer film by the polymer film production furnace, into contact with the catalyst according to any one of [1] to [8], which is provided inside or outside the furnace, at a temperature in the range of 180 to 350° C. to decompose the organic substances oxidatively; and a step 2 of refluxing all of or a part of a resultant decomposition gas to the polymer film production furnace.
  • the catalyst of the present invention has effects as shown below.
  • FIG. 1 is an X-ray diffraction pattern showing the crystal structure of a manganese-based oxide having a cryptomelane structure according to the present invention.
  • FIG. 2 shows a reactor for evaluation of caprolactam decomposing properties.
  • FIG. 3 is a graph showing the course of a CO 2 formation rate due to caprolactam decomposition.
  • FIG. 4 is a graph showing the removal rate of caprolactam.
  • FIG. 5 shows a reactor for evaluation of PET oligomer decomposing properties.
  • FIG. 6 is a graph showing the course of a CO 2 formation rate due to PET oligomer decomposition.
  • FIG. 7 is a graph showing the removal rate of a PET oligomer.
  • FIG. 8 is a graph showing the BET specific surface areas of mixed oxides or composite oxides used in Examples and Comparative Examples.
  • An object to which the catalyst of the present invention is applied is a gas inside a polymer film production furnace, the gas containing volatile organic compounds (VOCs) and sublimable organic substances generated within the polymer film production furnace.
  • the polymer, film production furnace refers, for example, to a furnace for stretching a thin plate of a melt-extrudate of starting polymer chips, while heating the thin plate, thereby processing it into a film form.
  • the type of the polymer is not limited, and includes polymers in general which are formed into films by the above method.
  • Their examples include PET, polyamide (nylon), polyethylene, PVA, polypropylene, polyvinyl chloride, and polystyrene.
  • the average particle diameter refers to the average particle diameter of secondary particles measured by the laser method.
  • the specific surface area is a value measured by the BET method.
  • the catalyst of the present invention contains a mixed oxide composed of a manganese-based oxide, which contains manganese and potassium and has a cryptomelane structure, and copper oxide.
  • the cryptomelane structure is considered to be represented by a chemical formula KMn 8 O 16 .
  • this structure is as follows: Manganese oxide (MnO 6 ) having an octahedral structure containing Mn at the center forms a tunnel-shaped structure. A cross-section of the tunnel-shaped structure is in a nearly quadrilateral shape having two Mn's arranged in one side. That is, an eight-membered ring comprising Mn is provided. A side surface of the tunnel-shaped structure is shared with another adjacent tunnel-shaped structure. Within the tunnel-shaped structure, potassium is arranged so as to fulfill the above-mentioned chemical formula.
  • MnO 6 Manganese oxide having an octahedral structure containing Mn at the center forms a tunnel-shaped structure. A cross-section of the tunnel-shaped structure is in a nearly quadrilateral shape having two Mn's arranged in one side. That is, an eight-membered ring comprising Mn is provided. A side surface of the tunnel
  • Whether the cryptomelane structure is taken or not can be determined by X-ray diffraction (XRD).
  • XRD X-ray diffraction
  • the mixed oxide of the present invention is a physical mixture of the Mn-based oxide having the cryptomelane structure, and copper oxide.
  • the content of the copper oxide is preferably 10 to 30% by weight, more preferably 15 to 25% by weight, as CuO based on the mixed oxide. If the content is in the range of 10 to 30% by weight, the purification performance and the durability are enhanced.
  • the content of Cu can be found by XRF (fluorescent X-ray analysis).
  • the content of Mn is preferably 65 to 85% by weight, more preferably 70 to 80% by weight, as MnO 2 based on the mixed oxide. If the content is in the range of 65 to 85% by weight, the purification performance and the durability are enhanced.
  • the content of Mn can be found by XRF (fluorescent X-ray analysis).
  • the content of potassium is preferably 0.1 to 10% by weight, more preferably 0.5 to 5% by weight, based on the mixed oxide. If the content is in the range of 0.1 to 10% by weight, the purification performance and the durability are enhanced.
  • the content of K can be found by XRF (fluorescent X-ray analysis).
  • the average particle diameter of the mixed oxide is preferably 0.1 to 500 ⁇ m, more preferably 0.5 to 200 ⁇ m.
  • the average particle diameter a value measured by laser diffraction scattering is used.
  • the mixed oxide used has a specific surface area (BET specific surface area, before heat treatment) of preferably 200 m 2 /g or larger, more preferably 220 m 2 /g or larger. Further, the specific surface area after heating for 1 hour at 500° C. is preferably 85 m 2 /g or larger, more preferably 90 m 2 /g or larger. That is, the mixed oxide undergoing a smaller structural change when heated at a high temperature is preferred. If the specific surface area (before heat treatment) is less than 200 m 2 /g, the initial purification performance is not sufficient. If the specific surface area after heating for 1 hour at 500° C. is less than 85 m 2 /g, the durability is poor.
  • BET specific surface area, before heat treatment preferably 200 m 2 /g or larger, more preferably 220 m 2 /g or larger.
  • the specific surface area after heating for 1 hour at 500° C. is preferably 85 m 2 /g or larger, more preferably 90 m 2 /g or larger. That
  • the catalyst of the present invention can be supported on a support medium as will be described later.
  • a binder can be used.
  • the binder is not particularly limited, and a publicly known binder can be used. Examples of the binder usable are colloidal silica, alumina sol, titania sol, silica sol, boehmite, and zirconia sol.
  • the catalyst of the present invention does not exclude the incorporation of other components, if they do not impede the intended operational advantages.
  • the other components include noble metals such as Pt, Pd and Rh.
  • this catalyst can be used in a form in which it is supported on a support medium (carrier for supporting the catalyst).
  • the preferred support medium is of a form having heat resistance, a high contact efficiency, and a small pressure loss. It is concretely exemplified by a honeycomb, a sheet, a mesh, a pipe, a filter, a perforated metal, and a foam metal.
  • the material for the support medium is not particularly limited, but is preferably the one having heat resistance and corrosion resistance. Its examples include cordierite, alumina, silica, silica alumina, carbon fibers, metal fibers, glass fibers, ceramic fibers, stainless steel, and titanium.
  • the amount of the catalyst supported on the support medium if the support medium is a honeycomb, for example, is preferably 100 to 250 g/L, more preferably 140 to 200 g/L, per liter of the honeycomb. If the amount supported is less than 100 g/L, the performance is poor in terms of durability. A larger amount supported results in better durability, but from the viewpoint of productivity, the preferred amount supported is 250 g/L or less.
  • a first step is a step of preparing a slurry containing the mixed oxide and a binder component.
  • a subsequent second step is a step of coating a honeycomb with a predetermined amount of the slurry, and then drying the coated honeycomb at 100 to 200° C. to form a catalyst precursor containing the mixed oxide and the binder component.
  • a succeeding third step is a step of calcining the catalyst precursor in air at a temperature in the range of 200 to 500° C.
  • the catalyst of the present invention is disposed within a polymer film production furnace or a hot air circulation system, where it is brought into contact with hot air.
  • the hot air circulation system is a flow path on which hot air generated within the polymer film production furnace is once delivered out of the production furnace, and then returned again into the production furnace.
  • volatile and/or sublimable organic substances included within the production furnace or within the hot air circulation system are decomposed by the catalyst and converted into CO 2 and H 2 O.
  • the gas inside the furnace is purified.
  • a temperature range of 180 to 350° C., preferably 200 to 350° C., more preferably 210 to 350° C. is preferred.
  • the decomposition reaction of the volatile and/or sublimable organic substances does not proceed sufficiently, with the result that the undecomposed volatile and/or sublimable organic substances remain, or carbon monoxide (CO) tends to form.
  • CO carbon monoxide
  • the reaction proceeds sufficiently.
  • cooling is required until the temperature lowers to a temperature suitable for heat treatment of the resulting polymer film (i.e., normally 200 to 230° C.), thereby wasting energy.
  • SV space velocity
  • the usual SV is preferably 1,000 to 200,000 hr ⁇ 1 , more preferably 2,000 to 100,000 hr ⁇ 1 , depending on the concentration of the volatile and/or sublimable organic substances in question.
  • the gas treated with the catalyst (treated gas) is refluxed to the polymer film production furnace, if required. On this occasion, the total amount of the treated gas may be refluxed, or after a part of the treated gas is discharged and fresh air is introduced into the remaining gas, the resulting mixture may be refluxed.
  • a catalytic decomposition reaction gasification reaction for converting organic fine particles, which are a polymeric material, into a low molecular weight hydrocarbon
  • an oxidation reaction of the resulting low molecular weight hydrocarbon and
  • a combustion reaction of coke forming on the catalyst in association with the catalytic decomposition reaction are presumed to occur synergistically: (i) A catalytic decomposition reaction (gasification reaction) for converting organic fine particles, which are a polymeric material, into a low molecular weight hydrocarbon, (ii) an oxidation reaction of the resulting low molecular weight hydrocarbon, and (iii) a combustion reaction of coke forming on the catalyst in association with the catalytic decomposition reaction.
  • the polymer film production furnace targeted by the present invention refers to a furnace for stretching a thin plate, which is a melt-extrudate of starting polymer chips, while heating the thin plate, thereby processing it into a film form.
  • the type of the polymer is not limited, and includes polymers in general which are formed into films by the above method. Examples of the polymer include PET, polyamide (nylon), polyethylene, PVA, polypropylene, polyvinyl chloride, and polystyrene.
  • KCG-4P manufactured by Clariant: a mixed oxide containing a manganese-based oxide, which contains manganese and potassium and has a cryptomelane structure, and copper oxide, according to the present invention; its composition contains 73.0 to 79.0% by weight as MnO 2 , 20.0 to 24.0% by weight as CuO, and 1.0 to 3.0% by weight as K, based on the mixed oxide) (111.2 g), 117.0 g of SNOWTEX-C(Nissan Chemical Industries, Ltd.), and 71.8 g of deionized water were mixed to prepare a slurry.
  • This slurry was coated on a ceramic corrugated honeycomb (manufactured by Seibu Giken Co., Ltd., 200 cells/square inch) by washcoating, and the excess slurry was blown off by compressed air. Then, the coated honeycomb was dried for 3 hours at 150° C. in a dryer. Then, the dried honeycomb was calcined for 1 hour at 250° C. in air to obtain Catalyst 1 of a honeycomb type supporting a catalyst layer of the mixed oxide. The weight of the catalyst layer per liter of the honeycomb was 157 g.
  • Catalyst 3 of a honeycomb type supporting a catalyst layer of the mixed oxide according to the present invention was obtained by the same method as for Catalyst 1, except that a cordierite honeycomb (manufactured by NGK INSULATORS, LTD., 200 cells/square inch) was used as a base material.
  • the weight of the catalyst layer per liter of the honeycomb was 148 g.
  • ⁇ -alumina powder manufactured by Nikki-Universal Co., Ltd., average particle diameter 5 ⁇ m
  • alumina sol as a binder in solid form
  • deionized water 600 g
  • This slurry was coated on a cordierite honeycomb (produced by NGK INSULATORS, LTD., 200 cells/square inch) by washcoating, and the excess slurry was blown off by compressed air. Then, the coated honeycomb was dried for 3 hours at 150° C. in a dryer, and then calcined for 1 hour at 500° C.
  • the weight of the ⁇ -alumina layer per liter of the honeycomb was 40 g.
  • Comparative Catalyst 1 of a honeycomb type having 1.8 g/L of Pt supported on alumina was obtained.
  • Comparative Catalyst 1 is a catalyst which has been widely used in catalytic applications to purification of the interior of furnaces.
  • Mn-based oxide Activated manganese dioxide (manufactured by Japan Metals & Chemicals Co., Ltd., BET specific surface area 150 m 2 /g) was used as a Mn-based oxide.
  • This Mn-based oxide does not have a cryptomelane structure, and is substantially free from potassium (even if potassium is contained, it is in a trace amount corresponding to an impurity level).
  • the Mn-based oxide contain copper oxide.
  • 99.6 g of the Mn-based oxide, 117.0 g of SNOWTEX-C(manufactured by Nissan Chemical Industries, Ltd.), and 83.4 g of deionized water were mixed to prepare a slurry.
  • This slurry was coated on a ceramic corrugated honeycomb (manufactured by Seibu Giken Co., Ltd., 200 cells/square inch) by washcoating, and the excess slurry was blown off by compressed air. Then, the coated honeycomb was dried for 3 hours at 150° C. in a dryer. Then, the dried honeycomb was calcined for 1 hour at 250° C. in air to obtain Comparative Catalyst 2 of a honeycomb type supporting a catalyst layer of the Mn-based oxide. The weight of the catalyst layer per liter of the honeycomb was 134 g.
  • Comparative Catalyst 3 of a honeycomb type supporting a catalyst layer of the Mn-based oxide The weight of the catalyst layer per liter of the honeycomb was 179 g.
  • N-840 (manufactured by Clariant) was used as a mixed oxide containing copper oxide and a Mn-based oxide in which the Mn-based oxide contained potassium, but had no cryptomelane structure. 76.4 g of the mixed oxide, 84.0 g of SNOWTEX-C (manufactured by Nissan Chemical Industries, Ltd.), and 120.0 g of deionized water were mixed to prepare a slurry. This slurry was coated on a ceramic corrugated honeycomb (manufactured by Seibu Giken Co., Ltd., 200 cells/square inch) by washcoating, and the excess slurry was blown off by compressed air. Then, the coated honeycomb was dried for 3 hours at 150° C. in a dryer.
  • Comparative Catalyst 4 of a honeycomb type supporting a catalyst layer of the Mn-based oxide The weight of the catalyst layer per liter of the honeycomb was 157 g.
  • DAIPYROXIDE #7710 (manufactured by Dainichiseika Color & Chemicals Mfg. Co., Ltd.) was used as a composite oxide containing copper oxide and a Mn-based oxide in which potassium other than impurities was not contained and the Mn-based oxide had no cryptomelane structure. 80.2 g of the composite oxide, 88.2 g of SNOWTEX-C (manufactured by Nissan Chemical Industries, Ltd.), and 126.0 g of deionized water were mixed to prepare a slurry.
  • This slurry was coated on a ceramic corrugated honeycomb (manufactured by Seibu Giken Co., Ltd., 200 cells/square inch) by washcoating, and the excess slurry was blown off by compressed air. Then, the coated honeycomb was dried for 3 hours at 150° C. in a dryer. Then, the dried honeycomb was calcined for 1 hour at 250° C. in air to obtain Comparative Catalyst 5 of a honeycomb type supporting a catalyst layer of the Mn-based oxide. The weight of the catalyst layer per liter of the honeycomb was 141 g.
  • ⁇ -caprolactam decomposition tests of Catalysts 1 and 2 and Comparative Catalysts 1 to 5 were conducted.
  • ⁇ -caprolactam is a typical substance which is deposited and accumulated within a polyamide film production furnace, and the removal of this substance is desired.
  • a sample container 12 for holding a powder of ⁇ -caprolactam (indicated by S in the drawing) is disposed.
  • a catalyst 13 (cylindrical honeycomb catalyst; diameter 21 mm, length 50 mm) is installed in a reaction tube 11 .
  • a gas treated with the catalyst i.e., an exhaust gas
  • a gas collection container 17 connected to the reaction tube 11 via connection piping 16 , and is cooled there to 0 to 5° C. from outside.
  • the undecomposed ⁇ -caprolactam is recovered in a solid form into a sampling container 18 installed within the container 17 , and is weighed.
  • an exhaust pipe 19 connected to the gas collection container 17 continuously measures the concentration of CO 2 in the exhaust gas.
  • the CO 2 concentration was measured with Model 410 i manufactured by Thermo Fisher Scientific.
  • the reaction tube 11 With a mixed gas composed of an N 2 gas and an O 2 gas (volume ratio 80:20) being flowed through a gas introduction pipe 15 of the reactor, the reaction tube 11 is heated from outside so that the catalyst 13 reaches 210° C.
  • the mixed gas has a flow rate set so that its space velocity becomes 70,000 h ⁇ 1 .
  • the sample evaporation container 10 is heated and held at 170° C.
  • a sample inlet attached to the sample evaporation container is opened, the sample container 12 holding 0.4 g of ⁇ -caprolactam (manufactured by Wako Pure Chemical Industries, Ltd.) is placed within the sample evaporation container 10 , and then the sample inlet is closed promptly.
  • the ⁇ -caprolactam is melted and volatilized.
  • the volatilized ⁇ -caprolactam is transported to the catalyst 13 , which has been heated at 210° C., by the mixed gas introduced through the gas introduction pipe 15 , and is treated with the catalyst 13 .
  • One test lasts for 60 minutes from the charging of the s-caprolactam. During the 60-minute test, the CO 2 concentration in the exhaust gas is continuously measured. After a lapse of 60 minutes, the sample container 12 is taken out of the sample evaporation container 10 , and the amount of ⁇ -caprolactam after the test is weighed. From the weighed amount, the amount of the volatilized ⁇ -caprolactam is calculated.
  • the amount of CO 2 discharged during one test (i.e., V2(L)) is determined. From the amount of the volatilized ⁇ -caprolactam, moreover, the amount of CO 2 provided that all the volatilized ⁇ -caprolactam has been converted into CO 2 (i.e., V1(L)) is calculated. Based on these amounts, the CO 2 formation rate is calculated from the equation indicated below. The fact that this value is high means that a proportion in which ⁇ -caprolactam has been completely oxidized is high, that is, that the catalyst performance is high.
  • the sampling container 18 is weighed, and the amount of the undecomposed ⁇ -caprolactam is calculated. Then, the ⁇ -caprolactam removal rate is calculated from the equation shown below. A high value of this rate means that the concentration of ⁇ -caprolactam on the outlet side of the catalyst is low, thus demonstrating that the catalyst performance is high.
  • Catalysts 1 and 2 of the present invention were high in the CO 2 formation rate, and decreases in the CO 2 formation rate were minimal even after repeated measurements, as compared with Comparative Catalysts 1 to 5.
  • Catalysts 1 and 2 of the present invention were superior to Comparative Catalysts 1 to 5, as shown in Table 2 and FIG. 4 .
  • PET oligomer decomposition tests of Catalysts 1 and 3 and Comparative Catalyst 1 were conducted.
  • a sample container 22 for holding PET chips (indicated by S in the drawing) is disposed.
  • a catalyst 23 (cylindrical honeycomb catalyst; diameter 21 mm, length 50 mm) is installed in a reaction tube 21 .
  • an organosilicon bubbling device (not shown) is connected to an upstream side of an organosilicon gas introduction pipe 24 .
  • a downstream side of the organosilicon gas introduction pipe 24 is connected to a downstream side of a gas introduction pipe 25 , providing a structure in which an organosilicon gas generated by bubbling can be supplied into the reaction tube 21 .
  • the supplied organosilicon gas works as a substance poisonous to the catalyst.
  • KF-96L-1CS manufactured by Shin-Etsu Chemical Co., Ltd. is used as organosilicon, and volatilized by bubbling.
  • the gas treated with the catalyst i.e., an exhaust gas
  • the undecomposed PET oligomer is recovered in a solid form into a sampling container 28 installed within the container 27 , and is weighed.
  • an exhaust pipe 29 connected to the gas collection container 27 continuously measures the concentration of CO 2 in the exhaust gas.
  • the CO 2 concentration was measured with Model 410 i manufactured by Thermo Fisher Scientific.
  • the reaction tube 21 With a mixed gas composed of an N 2 gas and an O 2 gas (volume ratio 80:20) being flowed through the gas introduction pipe 25 of the reactor, the reaction tube 21 is heated from outside so that the catalyst 23 reaches 230° C.
  • the mixed gas has a flow rate set so that its space velocity becomes 35,000 h ⁇ 1 .
  • the sample evaporation container 20 is heated and held at 400° C.
  • a sample inlet attached to the sample evaporation container is opened, the sample container 22 holding 1.65 g of PET chips is placed in the sample evaporation container 20 , and then the sample inlet is closed promptly. As a result, the PET chips are melted to generate a PET oligomer.
  • the generated PET oligomer is transported to the catalyst 23 , which has been heated at 230° C., by the mixed gas introduced through the gas introduction pipe 25 , and is treated with the catalyst 23 .
  • the organosilicon gas is supplied into the reaction tube 21 via the organosilicon gas introduction pipe 24 . Consequently, the decomposition of the PET oligomer is performed under a poisonous environment due to the organosilicon gas.
  • One test lasts for 30 minutes from the charging of the PET chips. During the 30-minute test, the CO 2 concentration in the exhaust gas is continuously measured. After a lapse of 30 minutes, the sample container 22 is taken out of the sample evaporation container 20 , and the amount of the PET chips after the test is weighed. From the weighed amount, the amount of the volatilized PET chips is calculated.
  • the amount of CO 2 discharged during one test i.e., V2(L)
  • the amount of CO 2 provided that all the volatilized PET chips are converted into CO 2 i.e., V1(L)
  • the CO 2 formation rate is calculated from the equation indicated below. A high value of this rate means that a proportion in which the volatilized PET oligomer has been completely oxidized is high, namely, that the catalyst performance is high.
  • the sampling container 28 is weighed, and the amount of the undecomposed PET oligomer is calculated. Then, the PET oligomer removal rate is calculated from the equation shown below. A high value of this rate means that the concentration of the PET oligomer on the outlet side of the catalyst is low, thus demonstrating that the catalyst performance is high.
  • Comparative Catalyst 1 showed a high CO 2 formation rate at the initial stage, but this formation rate declined rapidly. This finding shows that Comparative Catalyst 1 is easily poisoned with organosilicon.
  • Catalysts 1 and 3 of the present invention were lower than the comparative catalyst in the initial CO 2 formation rate, but their decreases in the CO 2 formation rate were slower. That is, Catalysts 1 and 3 of the present invention were more resistant to poisoning by organosilicon, and were longer in catalyst life.
  • Catalysts 1 and 3 of the present invention were comparable to Comparative Catalyst 1, as shown in Table 4 and FIG. 7 .
  • the measurements made in the present 12 tests correspond to about 1 year of use in a general real furnace (depending on the type of a polymer film manufactured in a production furnace, the manufacturing conditions, and so on, however, the duration of use may be longer or shorter than 1 year).
  • the various mixed oxides and composite oxides used above were measured for the BET specific surface areas before heat treatment and after heat treatment performed for 1 hour at 500° C.
  • the BET specific surface areas were measured with TriStar II 3020 manufactured by Micromeritics. The results of the measurements are shown in FIG. 8 .
  • KCG-4P used in the Example had a specific surface area of more than 85 m 2 /g even after heat treatment performed for 1 hour at 500° C.
  • N-840 and DAIPYROXIDE #7710 had specific surface areas of more than 200 m 2 /g before heat treatment, but showed specific surface areas of less than 85 m 2 /g after heat treatment performed for 1 hour at 500° C. That is, KCG-4P proves to be smaller in structural change due to heat treatment than N-840 and DAIPYROXIDE #7710.

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