Classifications

• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
  • C09K3/00—Materials not provided for elsewhere
  • C09K3/10—Materials in mouldable or extrudable form for sealing or packing joints or covers
  • C09K3/1006—Materials in mouldable or extrudable form for sealing or packing joints or covers characterised by the chemical nature of one of its constituents
  • C09K3/1009—Fluorinated polymers, e.g. PTFE
• • C—CHEMISTRY; METALLURGY
  • 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
  • C08J3/00—Processes of treating or compounding macromolecular substances
  • C08J3/24—Crosslinking, e.g. vulcanising, of macromolecules
• • C—CHEMISTRY; METALLURGY
  • 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
  • C08J3/00—Processes of treating or compounding macromolecular substances
  • C08J3/28—Treatment by wave energy or particle radiation
• • C—CHEMISTRY; METALLURGY
  • 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
  • C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/16—Nitrogen-containing compounds
  • C08K5/17—Amines; Quaternary ammonium compounds
  • C08K5/18—Amines; Quaternary ammonium compounds with aromatically bound amino groups
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
  • C08K5/37—Thiols
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
  • C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
  • C08L27/12—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
  • C08L27/18—Homopolymers or copolymers or tetrafluoroethene
• • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
  • F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
  • F16J—PISTONS; CYLINDERS; SEALINGS
  • F16J15/00—Sealings
  • F16J15/02—Sealings between relatively-stationary surfaces
  • F16J15/06—Sealings between relatively-stationary surfaces with solid packing compressed between sealing surfaces
  • F16J15/10—Sealings between relatively-stationary surfaces with solid packing compressed between sealing surfaces with non-metallic packing
• • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
  • F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
  • F16J—PISTONS; CYLINDERS; SEALINGS
  • F16J15/00—Sealings
  • F16J15/02—Sealings between relatively-stationary surfaces
  • F16J15/06—Sealings between relatively-stationary surfaces with solid packing compressed between sealing surfaces
  • F16J15/10—Sealings between relatively-stationary surfaces with solid packing compressed between sealing surfaces with non-metallic packing
  • F16J15/102—Sealings between relatively-stationary surfaces with solid packing compressed between sealing surfaces with non-metallic packing characterised by material
• • C—CHEMISTRY; METALLURGY
  • 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
  • C08J2327/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers
  • C08J2327/02—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment
  • C08J2327/12—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
  • C08J2327/18—Homopolymers or copolymers of tetrafluoroethylene
• • C—CHEMISTRY; METALLURGY
  • 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
  • C08J2427/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers
  • C08J2427/02—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment
  • C08J2427/12—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
  • C08J2427/18—Homopolymers or copolymers of tetrafluoroethylene

Definitions

• the present invention relates to a perfluoroelastomer composition, a sealing material using the same, and a method for producing the same.
• a sealing material made of fluororubber As a sealing material (gasket, packing, etc.) used for various applications, a sealing material made of fluororubber is known, and a plasma etching apparatus or a plasma CVD apparatus constituting a semiconductor manufacturing apparatus is, for example, a process for processing a wafer.
• a sealing material for keeping the chamber in a vacuum a sealing material made of a perfluoroelastomer having excellent heat resistance and plasma resistance (decomposition resistance by plasma) is used among fluororubbers. Further, for example, an appropriate mechanical strength is also required for a sealing material used in a gate part that partitions a chamber and a transport part in a semiconductor manufacturing apparatus because compression and release are repeated.
• the mechanical strength of the sealing material made of fluororubber can be improved by adding an inorganic filler.
• an inorganic filler when a sealing material containing an inorganic filler is used for semiconductor manufacturing equipment as described above, even when a perfluoroelastomer having excellent plasma resistance is used, the perfluorocarbon of the sealing material is used in a harsh plasma environment. In some cases, the elastomer component may be etched by plasma. In this case, the blended inorganic filler is scattered in the chamber, which may cause problems such as contamination of the chamber and defective semiconductor products.
• Patent Document 1 contains a perfluoroelastomer and a polytetrafluoroethylene resin powder, and the composition for a sealing material of a plasma etching apparatus in which the amount of eluted metal after vulcanization is a predetermined value or less. Things are listed.
• the object of the present invention is to maintain mechanical strength (hardness and modulus) while maintaining good heat resistance (compression set properties) without blending inorganic fillers that can cause the above problems. It is an object to provide a perfluoroelastomer composition capable of forming an excellent sealing material, a sealing material using the composition, and a method for producing the same.
• the present invention provides the following perfluoroelastomer composition, a sealing material and a method for producing the same.
• A represents SO 2 , O, C ⁇ O, an alkylene group having 1 to 6 carbon atoms, a perfluoroalkylene group having 1 to 10 carbon atoms, or two It is a carbon-carbon bond that directly bonds the benzene ring.
• the NH 2 group and the OH group or SH group on the same benzene ring are adjacent to each other, and the NH 2 group and the OH group or SH group are In the meta or para position.
• At least one crosslinking agent selected from the group consisting of A perfluoroelastomer composition comprising:
• a sealing material comprising a crosslinked product of the perfluoroelastomer composition according to any one of [1] to [4].
• cross-linking step includes a step of cross-linking with ionizing radiation.
• the present invention it is possible to provide a perfluoroelastomer composition having good heat resistance (compression set) after crosslinking and excellent mechanical strength even when no inorganic filler is blended. .
• the perfluoroelastomer composition of the present invention can be suitably applied as a sealing material, particularly as a sealing material for use in semiconductor manufacturing equipment.
• Perfluoroelastomer used in the present invention includes a structural unit I derived from tetrafluoroethylene, a structural unit II derived from perfluoro (alkyl vinyl ether) or perfluoro (alkoxyalkyl vinyl ether), and a nitrile group-containing perfluoro It is a ternary copolymer containing a structural unit III derived from vinyl ether. According to the perfluoroelastomer composition containing the perfluoroelastomer as a main component, a crosslinked molded product (sealant or the like) having excellent plasma resistance can be provided.
• Perfluoro (alkyl vinyl ether) can have 1 to 5 carbon atoms in the alkyl group, such as perfluoro (methyl vinyl ether), perfluoro (ethyl vinyl ether), perfluoro (propyl vinyl ether), and the like. . Perfluoro (methyl vinyl ether) is preferable.
• Perfluoro (alkoxyalkyl vinyl ether) can have 3 to 11 carbon atoms bonded to the vinyl ether group (CF 2 ⁇ CFO—).
• CF 2 CFO (CF 2 ) 3 OC n F 2n + 1
• CF 2 CFOCF 2 CF (CF 3) O (CF 2 O) m C n F 2n + 1
• n is, for example, 1 to 5
• m is, for example, 1 to 3.
• the ratio of each structural unit in the perfluoroelastomer, the ratio of structural unit I / structural unit II / structural unit III is usually 50 to 74.8% / 25 to 49.8% / 0.2 to 5% in molar ratio. Preferably, it is 60 to 74.8% / 25 to 39.5% / 0.5 to 2%.
• the perfluoroelastomer composition of the present invention can also contain two or more perfluoroelastomers having different ratios of structural unit I / structural unit II / structural unit III.
• perfluoroelastomer a commercially available product can be used, and an example thereof is a trade name “PFE 131TZ” manufactured by Dyneon.
• a fluororesin is a resin having a fluorine atom in its molecule.
• PTFE polytetrafluoroethylene
• PFA tetrafluoroethylene-perfluoroalkyl vinyl ether copolymer
• FEP tetrafluoroethylene-hexa Fluoropropylene copolymer
• ETFE tetrafluoroethylene-ethylene copolymer
• PCTFE polychlorotrifluoroethylene
• ECTFE chlorotrifluoroethylene-ethylene copolymer
• PVDF polyvinylidene fluoride
• PVDF Polyvinyl fluoride
• PVDF vinylidene fluoride-hexafluoropropylene copolymer
• VDF-HFP-TFE vinylidene fluoride-hexafluoropropylene-tetrafluoroethylene copolymer
• VDF-HFP-TFE vinylidene fluoride-hexafluoropropylene-
• PFA and PTFE having a high melting point from the viewpoint of preventing the resin from melting and damaging properties such as compression set when a molded product is used at a high temperature.
• the fluororesin may contain a functional group.
• the functional group can be introduced, for example, by copolymerizing a monomer having the functional group. Copolymerization of a crosslinking site monomer as a monomer having a functional group is advantageous for further increasing the mechanical strength and the like of the crosslinked molded product of the perfluoroelastomer composition.
• the crosslinking site monomer can be a nitrile group-containing monomer, similar to the nitrile group-containing perfluorovinyl ether described above.
• nitrile group-containing polytetrafluoroethylene described in JP2013-177631A can be mentioned.
• the fluororesin may be a modified fluororesin such as “TFM modified PTFE” (manufactured by Dinion).
• the content of fluororesin in the perfluoroelastomer composition (the total amount when two or more fluororesins are used) is 1 to less than 25 parts by weight per 100 parts by weight of perfluoroelastomer, preferably 3 to 24 parts by weight, more preferably 3 to 20 parts by weight. Setting the amount to 1 part by weight or more is advantageous in increasing the mechanical strength of the obtained crosslinked molded product (sealant or the like). Further, when the content is less than 25 parts by weight, both good mechanical strength and good heat resistance (compression set characteristics) can be achieved. When the content of the fluororesin is 25 parts by weight or more, the content of the perfluoroelastomer exhibiting elasticity is relatively reduced and the compression set characteristics are deteriorated.
• the fluororesin content of 1 part by weight or more and less than 25 parts by weight is a relatively small content
• excellent mechanical strength can be obtained by applying a crosslinking system based on a predetermined crosslinking agent described later. Can be realized.
• the perfluoroelastomer composition of the present invention includes a bis (aminophenol) compound represented by the above general formula (1), a bis (aminothiophenol) compound represented by the above general formula (2), and the above It contains at least one crosslinking agent selected from the group consisting of tetraamine compounds represented by general formula (3).
• a cross-linking system based on this cross-linking agent, a perfluoroelastomer having a nitrile group as a cross-linking site is cross-linked, so that a cross-linked molded article having excellent mechanical strength despite a relatively low fluororesin content. Can be granted.
• cross-linking of the fluororesin also proceeds by the cross-linking agent, which can contribute to further improvement of mechanical strength.
• crosslinking agent examples include, for example, 2,2-bis (3-amino-4-hydroxyphenyl) hexafluoropropane (BOAP); 4,4′-sulfonylbis (2-aminophenol) [bis ( 3-amino-4-hydroxyphenyl) sulfone], 3,3′-diaminobenzidine, 3,3 ′, 4,4′-tetraaminobenzophenone.
• BOAP 2,2-bis (3-amino-4-hydroxyphenyl) hexafluoropropane
• 4,4′-sulfonylbis (2-aminophenol) bis ( 3-amino-4-hydroxyphenyl) sulfone]
• 3,3′-diaminobenzidine 3,3 ′, 4,4′-tetraaminobenzophenone.
• BOAP is used.
• the content of the cross-linking agent in the perfluoroelastomer composition (the total amount when two or more cross-linking agents are used) cross-links all the cross-linking sites of the perfluoroelastomer (and in some cases, the cross-linking sites of the fluororesin). It is preferable that the amount is sufficient, typically 0.05 to 5 parts by weight, more preferably 0.1 to 3 parts by weight per 100 parts by weight of the perfluoroelastomer. More preferably, it is 0.1 to 1.5 parts by weight.
• the perfluoroelastomer composition may contain a crosslinking agent or crosslinking catalyst other than the above general formulas (1) to (3).
• a crosslinking agent or crosslinking catalyst other than the above general formulas (1) to (3).
• a tin compound, a phosphorus compound, or a nitrogen compound that is a triazine crosslinking catalyst. Can be included.
• the content of the other crosslinking agent or crosslinking catalyst is 50% by weight or less with respect to 100% by weight of the crosslinking agent of the above general formulas (1) to (3) from the viewpoint of the mechanical strength of the crosslinked molded product. It is preferably 20% by weight or less, more preferably 10% by weight or less, and particularly preferably 0% by weight.
• the perfluoroelastomer composition of the present invention is used for the purpose of improving processability, adjusting physical properties, etc., as necessary, with anti-aging agents, antioxidants, vulcanization accelerators, processing aids ( Stearic acid, etc.), stabilizers, tackifiers, silane coupling agents, plasticizers, flame retardants, mold release agents, waxes, lubricants and the like. Only 1 type may be used for an additive and it may use 2 or more types together.
• the amount of additive is preferably as small as possible.
• 10 parts by weight or less per 100 parts by weight of perfluoroelastomer preferably 5 parts by weight or less, more preferably 2 parts by weight or less, and even more preferably 1 part by weight or less
• the perfluoroelastomer composition of the present invention may be carbon black, silica, alumina, zinc oxide, titanium oxide, clay, talc, diatomaceous earth, barium sulfate, calcium carbonate, magnesium carbonate, calcium oxide, mica, if necessary. It can also contain fillers such as graphite, aluminum hydroxide, aluminum silicate, hydrotalcite, metal powder, glass powder, ceramic powder.
• the amount of inorganic filler is preferably as small as possible (for example, 10 parts by weight or less, preferably 5 parts by weight or less, more preferably 2 parts by weight or less, and further preferably 1 part by weight or less) per 100 parts by weight of the perfluoroelastomer, and it is desirable that no inorganic filler is blended.
• the inorganic filler refers to a filler containing a metal element (Ba, Ti, Zn, Al, Mg, Ca, Si, etc.).
• the perfluoroelastomer composition of the present invention is obtained by uniformly kneading a perfluoroelastomer, a fluororesin, a crosslinking agent, and other compounding agents added as necessary.
• a perfluoroelastomer for example, a conventionally known one such as a mixing roll such as an open roll; a mixer such as a kneader or a Banbury mixer can be used.
• compounding agents may be mixed and kneaded at one time, or after kneading a part of the compounding agents, kneading all the compounding agents in multiple stages such as kneading the remaining compounding agents. You may do it.
• kneading of perfluoroelastomer and fluororesin for example, 1) a method of kneading perfluoroelastomer powder and fluororesin powder using a mixing roll, 2) perfluoroelastomer powder or pellets and fluororesin powder or pellets In addition to the melt kneading method using a mixer, 3) a method of adding a fluororesin in the preparation stage of the perfluoroelastomer can be used.
• a crosslinked molded product such as a sealing material can be obtained by crosslinking (vulcanizing) the perfluoroelastomer composition.
• Crosslinking molding can be performed by preforming a perfluoroelastomer composition as necessary and then press molding using a mold.
• the molding temperature is, for example, about 150 to 220 ° C.
• Molding may be performed by feed press molding, injection molding, extrusion molding, or the like. If necessary, secondary crosslinking may be performed at a temperature of about 150 to 280 ° C.
• perfluoroelastomer composition examples include ETFE, PVDF, PCTFE, ECTFE, vinylidene fluoride-hexafluoropropylene copolymer (VDF-HFP copolymer), vinylidene fluoride-hexafluoropropylene-tetrafluoroethylene copolymer (
• VDF-HFP copolymer vinylidene fluoride-hexafluoropropylene-tetrafluoroethylene copolymer
• the above-described cross-linking molding (press molding) Etc.) is preferably further provided with a step of crosslinking by irradiation with ionizing radiation.
• the ionizing radiation electron beams and ⁇ rays can be preferably used.
• Sealing material can be packing or gasket.
• the shape of the sealing material is appropriately selected according to the application, and a typical example is an O-ring having a cross-sectional shape of O-type. Since the sealing material according to the present invention may have good heat resistance (compression set characteristics) and mechanical strength while containing no inorganic filler, it is particularly suitable as a sealing material for use in semiconductor manufacturing equipment. Can be used.
• FFKM1 Tetrafluoroethylene / perfluoro (alkyl vinyl ether) / nitrile group-containing perfluoroelastomer which is a nitrile group-containing perfluoro (alkyl vinyl ether) copolymer (“PFE-131TZ” manufactured by Dyneon).
• FFKM2 A mixture of perfluoroelastomer and fluororesin [“PFE-133TBZ” manufactured by Dyneon].
• the perfluoroelastomer is a nitrile group-containing perfluoroelastomer which is a tetrafluoroethylene / perfluoro (alkyl vinyl ether) / nitrile group-containing perfluoro (alkyl vinyl ether) copolymer.
• Table 1 shows the content (parts by weight) of the perfluoroelastomer contained in FFKM2 in the column “FFKM2”, and the content (parts by weight) of the fluororesin contained in FFKM2 in the column “Fluororesin 1”. ).
• FFKM3 “PFR94” manufactured by Solvay Specialty Polymers.
• Fluororesin 2 Polytetrafluoroethylene micropowder (“TF9207Z” manufactured by Dyneon).
• BOAP 2,2-bis (3-amino-4-hydroxyphenyl) hexafluoropropane [Tokyo Chemical Industry Co., Ltd., “2,2-Bis (3-amino-4-hydroxyphenyl) hexafluoropropane (CAS number: 83558) -87-6)]]].
• Triazine crosslinking catalyst “PFE300C” manufactured by Dyneon.
• TAIC triallyl isocyanurate [Nippon Kasei Co., Ltd. “TAIC”].
• Perhexa 25B 2,5-dimethyl-2,5-di (t-butylperoxy) hexane [“Perhexa 25B” manufactured by NOF Corporation].

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• Chemical Kinetics & Catalysis (AREA)
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• Polymers & Plastics (AREA)
• Engineering & Computer Science (AREA)
• General Engineering & Computer Science (AREA)
• Materials Engineering (AREA)
• Mechanical Engineering (AREA)
• Sealing Material Composition (AREA)
• Compositions Of Macromolecular Compounds (AREA)
• Gasket Seals (AREA)
• Treatments Of Macromolecular Shaped Articles (AREA)

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• 2013
  • 2013-12-27 JP JP2013271345A patent/JP6230415B2/ja active Active
• 2014
  • 2014-11-13 KR KR1020167014841A patent/KR20160104620A/ko not_active Withdrawn
  • 2014-11-13 CN CN201480070928.5A patent/CN105899600B/zh active Active
  • 2014-11-13 US US15/108,110 patent/US20160319102A1/en not_active Abandoned
  • 2014-11-13 EP EP14873637.4A patent/EP3088460A4/en not_active Withdrawn
  • 2014-11-13 SG SG11201605257UA patent/SG11201605257UA/en unknown
  • 2014-11-13 WO PCT/JP2014/080026 patent/WO2015098337A1/ja not_active Ceased
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