Classifications

• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B27/00—Layered products comprising a layer of synthetic resin
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B27/00—Layered products comprising a layer of synthetic resin
  • B32B27/18—Layered products comprising a layer of synthetic resin characterised by the use of special additives
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B32—LAYERED PRODUCTS
  • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
  • B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
  • B32B7/04—Interconnection of layers
  • B32B7/06—Interconnection of layers permitting easy separation
• • 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
  • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
  • C08J5/18—Manufacture of films or sheets
• • 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
  • 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
  • C08J7/04—Coating

Definitions

• the present invention relates to a film excellent in removing the release layer provided on the film, and a method for producing a recovery film using the same.
• MLCC multilayer ceramic capacitors
• the general manufacturing method of MLCC is that first, a ceramic green sheet and an electrode are laminated on a release film having a release layer provided on a film as a base material, dried and hardened, and the ceramic green sheet and the electrode are formed. After forming the laminate (released object), the laminate is peeled off from the release film.
• a plurality of layers are laminated and fired on a laminated body composed of a ceramic green sheet peeled from a release film and electrodes.
• the release film is discarded as an unnecessary substance after the layer consisting of the ceramic green sheet and the electrode is peeled off.
• Patent Document 1 discloses a technique in which wax is kneaded into a film and used as a release film. Further, Patent Document 2 discloses a method of cleaning a release film with a metal brush and reusing it.
• the release agent when wax is used as the release agent, the coating property of the ceramic slurry for forming the ceramic green sheet to be released and the peelability of the green sheet obtained by drying the slurry are not sufficient. Further, since wax is a substance different from the components constituting the film, there is a problem that it becomes a foreign substance at the time of remelting. Further, when the release film is washed with a metal brush, there are problems that the release film cannot be washed uniformly and the release layer is not sufficiently removable.
• the present invention has the following configuration. That is, [I] A film having a thickness of 500 ⁇ m or less, which has an absorption peak having an absorption peak of 10% or more at the peak having a wavelength of 800 nm or more and 1200 nm or less, or an average absorbance of 15% or more having a wavelength of 800 nm or more and 1200 nm or less. [II] The film according to [I], wherein at least one surface has a contact angle with water of 90 ° or more. [III] The film according to [I] or [II], which has a layer containing a thermoplastic resin as a main component (base material layer) having a melting point of 250 ° C.
• a release layer is provided on the film, then a release material is provided on the release layer of the film having the release layer, and then a release material is provided from the film having the release layer having the release material.
• [X] The residue of the release material and the release layer are removed from the film having the release layer obtained by releasing the release material by irradiation with a laser having an oscillation wavelength of 800 nm or more and 1200 nm or less.
• [XI] The method of using the film according to any one of [I] to [X].
• a method of using a film which comprises a step of removing a residue of a release material and a release layer from a film having a release layer obtained by releasing the release material.
• [XII] A method for producing a recovery film using the film according to any one of [I] to [X].
• a method for producing a recovery film which comprises a step of removing a residue of a release material and a release layer from a film having a release layer obtained by releasing the release material.
• a film to be released is provided with a mold release object, then the mold release material is released from the film having the mold release material, and then the residue and infrared rays of the mold release material are released from the film from which the mold release material is released.
• the layer containing the residue of the release product and the infrared absorber is removed from the film from which the mold release material is released by irradiation with a laser having an oscillation wavelength of 800 nm or more and 1200 nm or less.
• [XVI] The method of using the film according to [XIII] to [XV].
• a film having good coatability such as a ceramic slurry and excellent in removing a release layer from a substrate after use and a method for producing a recovery film using such a film. Can be done.
• the film of the present invention preferably contains a resin as a main component.
• the resin used in the present invention may be either a thermoplastic resin or a thermosetting resin, but a thermoplastic resin is preferable from the viewpoint of good moldability.
• thermoplastic resin examples include polyethylene, polypropylene, poly (1-butene), poly (4-methylpentene), polyisobutylene, polyisoprene, polybutadiene, polyvinylcyclohexane, polystyrene, poly ( ⁇ -methylstyrene), and poly (p-).
• Methylstyrene Polynorbornene, Polycyclopentene and other polyolefins, Nylon 6, Nylon 11, Nylon 12, Nylon 66 and other polyamides, ethylene / propylene copolymers, ethylene / vinylcyclohexane copolymers, ethylene / vinylcyclohexene copolymers, ethylene / alkyl Vinyl monomer copolymers such as acrylate copolymers, ethylene / acrylic methacrylate copolymers, ethylene / norbornene copolymers, ethylene / vinyl acetate copolymers, propylene / butadiene copolymers, isobutylene / isoprene copolymers, vinyl chloride / vinyl acetate copolymers, polyacrylates, polys.
• Acrylic polyethylene terephthalate represented by methacrylate, polymethyl methacrylate, polyacrylamide, polyacrylonitrile, etc., polypropylene terephthalate, polybutylene terephthalate, polyethylene-2, 6-naphthalate, etc., polyester, polyethylene oxide, polypropylene oxide, polyacry Biodecomposition typified by polyethers typified by len glycol, diacetyl cellulose, triacetyl cellulose, propionyl cellulose, butyryl cellulose, acetylpropionyl cellulose, cellulose esters typified by nitrocellulose, polylactic acid, polybutyl succinate, etc.
• Sex Copolymers Others, Polyvinyl Chloride, Vinylidene Chloride, Polyvinyl Alcohol, Polyvinyl Butyral, Polyacetal, Polyglucolic Acid, Polycarbonate, Polyketone, Polyether Sulfone, Polyether Ether Ketone, Modified Polyphenylene Ether, Polyphenylene Sulfide, Polyetherimide, Polyethylene , Polysiloxane, ethylene tetrafluoride, ethylene trifluoride, ethylene trifluoride, ethylene tetrafluoride-6, propylene fluoride copolymer, polyvinylidene fluoride and the like can be used.
• polyolefin, acrylic, polyester, cellulose ester, polyvinyl butyral, polycarbonate, and polyether sulfone are more preferable, and polyester is more preferable from the viewpoint of strength, moldability, and heat resistance.
• the polyester referred to in the present invention has a dicarboxylic acid component and a diol component.
• a constituent component means the smallest unit which can be obtained by hydrolyzing polyester.
• the dicarboxylic acid constituents constituting the polyester include terephthalic acid, isophthalic acid, phthalic acid, 1,4-naphthalenedicarboxylic acid, 1,5-naphthalenedicarboxylic acid, 2,6-naphthalenedicarboxylic acid, and 1,8-naphthalene.
• aromatic dicarboxylic acids such as dicarboxylic acid, 4,4'-diphenyldicarboxylic acid and 4,4'-diphenylether dicarboxylic acid, or ester derivatives thereof.
• PET polyethylene terephthalate
• PEN polyethylene-2,6-naphthalenedicarboxylate
• isophthalic acid and naphthalenedicarboxylic acid as part of the dicarboxylic acid component of PET are used as polyesters.
• polyester obtained by copolymerizing cyclohexanedimethanol, spiroglycol, or diethylene glycol as part of the diol component of PET is preferably used.
• the film of the present invention needs to have an absorption peak with a peak top of 800 nm or more and 1200 nm or less having an absorption peak of 10% or more, or an average absorbance of 800 nm or more and 1200 nm or less of 15% or more.
• the film of the present invention may have an absorption peak having an absorption peak of at least a peak with a wavelength of 800 nm or more and 1200 nm or less having an absorption peak of 10% or more, or an average absorbance having a wavelength of 800 nm or more and 1200 nm or less of 15% or more.
• a film having an absorption peak with a peak top of 800 nm or more and 1200 nm or less having an absorption peak of 10% or more and an average absorption peak of 800 nm or more and 1200 nm or less having an average absorbance of 15% or more is naturally included in the present invention. Is done. More preferably, the absorptivity of the peak top of the absorption peak is more preferably 15% or more, and further preferably 20% or more. Further, the average absorptivity having a wavelength of 800 nm or more and 1200 nm or less is preferably 20% or more.
• the release layer can be easily removed by irradiating a laser beam having an oscillation wavelength at a wavelength of 800 nm or more and 1200 nm or less.
• the film of the present invention needs to have a thickness of 500 ⁇ m or less. If it exceeds 500 ⁇ m, the handleability when removing the release layer may be inferior. It is preferably 250 ⁇ m or less, more preferably 100 ⁇ m or less, still more preferably 37 ⁇ m or less, and most preferably 24 ⁇ m or less. If the thickness of the film becomes thin, the strength becomes insufficient, and the release layer may not be removed or the film may not be conveyed. Therefore, the thickness is preferably 10 ⁇ m or more.
• the film of the present invention preferably has a contact angle with water of 90 ° or more on at least one surface.
• the peelability becomes good when the film of the present invention is used as a release film.
• the upper limit of the water contact angle is not particularly set, but it is preferably 110 ° or less. If it exceeds 110 °, when the ceramic slurry is applied on the film, the slurry may be repelled and a green sheet may not be obtained.
• a method of providing a layer containing an infrared absorber a method of providing a base material layer and a layer containing an infrared absorber by coextrusion, or a method of gravure coating and Mayer a layer containing an infrared absorber on the base material layer. Examples thereof include a method of providing by coating such as bar coating, air knife coating, doctor knife coating, and spin coating.
• the preferable layer thickness ratio of the base material layer and the layer containing the infrared absorber is the thickness of the base material layer (thickness of the base material layer / infrared absorber) with respect to the thickness of the layer containing the infrared absorber.
• the thickness of the layer containing the above) is 10 or more. More preferably, it is 15 or more.
• the upper limit of the thickness ratio is preferably 1000 or less.
• the base material layer contains polyester as a main component because the handleability can be particularly improved and the release layer can be easily removed by the method described later.
• the base material layer preferably has an average absorbance of 10% or less at a wavelength of 800 nm or more and 1200 nm or less.
• the absorbance of the base material layer By setting the absorbance of the base material layer to such a range, when the film of the present invention is irradiated with a laser having an oscillation wavelength of 800 nm or more and 1200 nm or less, energy is concentrated on the layer containing the infrared absorber. Therefore, not only the removability is improved, but also the deterioration of the resin constituting the base material layer can be suppressed. More preferably, it is 8% or less.
• Examples of the infrared absorber in the film of the present invention include metals such as Al, Cu, Au, Ag, and Ti, inorganic substances such as carbon black, and dyes containing organic substances as main components.
• the layer containing the infrared absorber is irradiated with a laser having an oscillation wavelength of 800 nm or more and 1200 nm or less, the infrared absorber absorbs infrared rays and has heat energy. Therefore, the layer containing the infrared absorber or adjacent to the layer. If there are layers, those layers are likely to be destroyed and removed.
• the infrared absorber in the film of the present invention preferably has sublimation properties.
• the volume of the infrared absorber rapidly increases.
• the sublimation temperature of the infrared absorber is preferably 280 ° C. or higher and 400 ° C. or lower.
• the infrared absorber may sublimate in the step of using the film of the present invention as the release film (such as the step of providing the release object on the film), and the release film It may not be possible to use as. If the temperature exceeds 400 ° C., the energy required for sublimation by the infrared absorber may increase, so that the removal performance of the release layer may be inferior. Further, the infrared absorber preferably has a phthalocyanine skeleton. Having a phthalocyanine skeleton is preferable because it is highly soluble in an organic solvent such as toluene or ethanol, and the base material layer can be coated with the solvent at a high concentration.
• the layer containing the infrared absorber may contain a substance that is easily vaporized by the thermal energy generated by the infrared absorber absorbing light having a wavelength of 800 nm to 1200 nm.
• a substance that easily vaporizes for example, nitrocellulose is preferably used.
• the infrared absorber has sublimation properties, the substance that is easily vaporized by the sublimating energy is also vaporized, and the layer adjacent to the layer containing the infrared absorber can be efficiently removed.
• the layer containing the infrared absorber contains a release agent.
• a release agent By impregnating the layer containing the infrared absorber with the release agent, it is not necessary to separately provide a release layer having good releasability, so that a film having excellent process stability can be obtained.
• the release agent used in the present invention include an alkyd resin-based release agent, a polyolefin-based release agent, a long-chain alkyl group-containing resin-based release agent, a fluorine-based release agent, a silicone-based release agent, and an organic-based release agent. And silicone-based mixture or copolymer resin-based mold release agent.
• a silicone release agent is particularly preferably used from the viewpoint of the coatability of the ceramic slurry used for producing the ceramic green sheet and the peelability of the ceramic green sheet obtained by drying and solidifying the ceramic slurry.
• a method of melt-forming polyester can be preferably used for the layer containing polyester as a main component. That is, the layer containing polyester as a main component is sequentially biaxially stretched or simultaneously biaxially stretched at a temperature equal to or higher than the glass transition point of polyester in a step of cooling and solidifying the polyester from a molten state to obtain a sheet, and a step of stretching.
• a polyester film obtained by undergoing a step of heat-treating at a temperature equal to or lower than the melting point of polyester can be used.
• a method of providing a layer containing an infrared absorber will be described.
• the infrared absorber is dissolved in a solvent such as toluene or methyl ethyl ketone (MEK), and a solution sufficiently stirred with a homogenizer or the like is applied onto the base material layer by coating.
• a solvent such as toluene or methyl ethyl ketone (MEK)
• MEK methyl ethyl ketone
• a solution sufficiently stirred with a homogenizer or the like is applied onto the base material layer by coating.
• a solution sufficiently stirred with a homogenizer or the like is applied onto the base material layer by coating.
• a silicone mold release agent having an addition reaction curing type polysiloxane structure by heating is preferable because it has high solubility in toluene, MEK, etc. and is easily contained in a layer containing an infrared absorber. ..
• the film of the present invention can be obtained by applying a solution containing an infrared absorber and a silicone resin obtained as described above onto a polyester film by coating and drying in an oven or the like to evaporate the solvent. it can.
• a coating method a general coating method such as gravure coating, Mayer bar coating, air knife coating, and doctor knife coating can be used.
• a layer containing an infrared absorber and a release layer are separately provided.
• the contact angle of the film of the present invention with water can be set in a preferable range. It is preferable because it can be done.
• the method of providing the layer containing the infrared absorber is to prepare a film in which the layer containing the infrared absorber is provided in advance by in-line coating, and then prepare the film.
• a method of providing a layer containing a release agent as a release layer, or a layer containing an infrared absorber and a layer containing a release agent as a release layer are simultaneously in-line coated with two layers using a die or the like. There is a method of providing.
• the layer containing the infrared absorber When the layer containing the infrared absorber is provided by in-line coating, it is preferable to disperse the infrared absorber in polyester resin, polycarbonate resin, epoxy resin, alkyd resin, acrylic resin, urea resin, and urethane resin.
• an acrylic resin is preferable from the viewpoint of dispersibility.
• the resin in which the above-mentioned infrared absorber is dispersed is preferably an emulsion type dispersed in water from the viewpoint of environmental protection, resource saving, and exhaustion problem of organic solvent at the time of production. Further, from the viewpoint of adhesion to the film as the base material, it is also a preferable embodiment to add an oxazoline resin, a melamine resin, an epoxy resin, a carbodiimide resin, or an isocyanate resin as a cross-linking agent.
• each layer is provided by in-line coating, from the viewpoint of drying the coating film, when the film as the base material layer is obtained by simultaneous biaxial stretching, it is applied to the film before stretching, and when it is obtained by sequential biaxial stretching, the longitudinal stretching step is performed. It is preferable to apply it later.
• the mold to be released on the film of the present invention is formed of a ceramic slurry made of a dielectric paste.
• a dielectric paste As a dielectric raw material, powders of various compounds to be composite oxides and oxides, such as carbonates, nitrates, hydroxides, and organic metal compounds, are kneaded with an organic vehicle to form a paste. It is the one that was made.
• the organic vehicle is a binder resin dissolved in an organic solvent.
• a polyvinyl butyral resin is preferably used from the viewpoint of coatability.
• the organic solvent used in the organic vehicle is not particularly limited, and for example, an organic solvent such as terpineol, alcohol, butyl carbitol, acetone, and toluene is used.
• the ceramic slurry composed of the dielectric paste is provided on the film of the present invention by coating by a die coating method, a doctor blade method, etc., dried at a temperature of 50 ° C. to 100 ° C. to form a sheet, and then peeled off. ..
• the peeling method is not particularly limited, but is generally performed by making a notch in a predetermined size to be peeled and sucking.
• a release layer is provided on the film of the present invention, a mold release material is provided on the film, and then the mold release material is released, and then the residue of the mold release material and infrared rays are provided from the film. It can be suitably used for removing a layer containing an absorbent.
• the method for removing the residue of the demolded material and the layer containing the infrared absorber from the film of the present invention is preferably performed by irradiation with a laser having an oscillation wavelength of 800 nm or more and 1200 nm or less.
• the layer containing the infrared absorber of the film of the present invention efficiently absorbs the photon energy of the laser, and the layer decomposes and foams. ..
• the layer that absorbs infrared rays, the layer adjacent thereto, and the layer adjacent thereto can be destroyed and removed.
• the recovery film By destroying and removing the layer that absorbs infrared rays, the layer adjacent to it, and the layer adjacent to it (the release layer and the residue of the demolded object), only the film that is the base material (hereinafter referred to as the recovery film). It becomes possible to obtain).
• the recovered film is remelted and then made into chips, which are used as a recycled material for film formation, and are reused as a film for various purposes such as providing a layer containing a release agent on the film again. It is possible to reduce waste and oil resource consumption.
• a mold release agent is contained in the layer containing the infrared absorber of the film of the present invention, a mold release agent is provided on the film, and after the mold release material is released, the mold release material is released from the film. It can be suitably used for removing a layer containing a residue and an infrared absorber.
• the light of a laser having an oscillation wavelength of 800 nm or more and 1200 nm or less is specifically absorbed by a layer having an absorption peak at a wavelength of 800 nm or more and 1200 nm or less, particularly a layer containing an infrared absorber. Irradiation may be performed from the base material side of the film of the present invention or from the side where the releaseable substance residue is present.
• the laser may be a pulse wave or a continuous wave, but it is preferable that the laser is a continuous wave from the viewpoint of continuously and evenly irradiating the film. Further, the oscillation intensity of the laser light is preferably 5 W or more and 50 W or less from the viewpoint of the reactivity efficiency of the layer containing the infrared absorber.
• the irradiation time is not particularly limited, but it is preferable to irradiate for 0.1 seconds or longer.
• the film of the present invention As described above, after removing the residue of the mold release substance and the release layer from the film of the present invention, it is possible to obtain only the film as the base material (recovery film). As a result, the recovered film is remelted and then made into chips, which are used for film formation as a recycled material, or are reused as a film by providing a layer containing a mold release agent on the film again, thereby producing waste. It is possible to reduce the consumption of oil resources.
• the transmittance of the film is subtracted from 100 to obtain the absorbance of the film.
• the absorbance of the film In the range of 800 nm to 1200 nm, if there is a peak with a half width of 100 nm or less, the peak top absorptivity is obtained, and if there is no peak, the average value of the 800 nm to 1200 nm absorptivity is obtained and used as the film absorptivity.
• each layer of film was a laminated film
• the thickness of each layer was determined by the following method. A cross section of the film is cut out with a microtome in a direction parallel to the film width direction. The cross section is observed with a scanning electron microscope at a magnification of 5000 times, and the thickness of each laminated layer is measured.
• the obtained dielectric paste is applied onto the film of the present invention with a die coater so that the thickness after drying is 2 ⁇ m, dried, and wound to obtain a green sheet with a release film.
• the wound green sheet is unwound and visually observed without being peeled off from the release film, and the presence or absence of pinholes and the coating state of the sheet surface and edges are confirmed.
• the area to be observed is 300 mm in width and 500 mm in length.
• the green sheet molded on the release film is illuminated from the back with a backlight unit of 1000 lux, and pinholes due to omission of coating are observed and evaluated as follows.
• A has good manufacturability.
• A There are 5 or less pinholes.
• B 6 or more pinholes.
• release layer E The film after peeling the demolded object by the method described in the section is irradiated with laser light. While irradiating, it sucks dust and the like generated on the film surface.
• Example 12 the same evaluation was performed based on the F element concentration (atomic%) on the film surface on the release layer side after laser irradiation.)
• F-2 Regarding the film surface on the release layer side after laser irradiation, B.I.
• the contact angle of water was calculated in the same manner as in the section. The lower the contact angle of water on the release layer side after laser irradiation, the more the release layer is removed.
• melt-polymerized PET Polymerization was carried out from terephthalic acid and ethylene glycol using antimony trioxide as a catalyst by a conventional method to obtain melt-polymerized PET.
• the obtained melt-polymerized PET had a glass transition temperature of 81 ° C., a melting point of 255 ° C., an intrinsic viscosity of 0.62, and an amount of terminal carboxyl groups of 20 eq. It was / t.
• PET-A 0.3 parts by weight of an infrared absorber FDN-010 (phthalocyanine vanadium complex, sublimation temperature 340 ° C.) manufactured by Yamada Chemical Co., Ltd. was added to 99.7 parts by weight of PET-1. Kneading was carried out in an extruder with a vent hole while maintaining the pressure at 1 kPa or less to obtain PET-A containing an infrared absorber.
• the glass transition temperature is 81 ° C.
• the melting point is 255 ° C.
• the intrinsic viscosity is 0.61
• the amount of terminal carboxyl groups is 30 eq. It was / t.
• PET-B 1 part by weight of an infrared absorber FDN-010 (phthalocyanine vanadium complex, sublimation temperature 340 ° C.) manufactured by Yamada Chemical Co., Ltd. is added to 99 parts by weight of PET-1 and extruded with a vent hole. Kneading was carried out in a machine while maintaining the pressure at 1 kPa or less to obtain PET-B containing an infrared absorber.
• the glass transition temperature is 81 ° C.
• the melting point is 255 ° C.
• the intrinsic viscosity is 0.59
• the amount of terminal carboxyl groups is 38 eq. It was / t.
• coating agent A 100 parts by weight of an addition reaction type silicone resin release agent (trade name: LTC750A manufactured by Toray Dow Corning Silicone Co., Ltd., having a polysiloxane structure), platinum catalyst (Toray Dow Corning Silicone (Toray Dow Corning Silicone) 2 parts by weight of trade name SRX212) manufactured by Co., Ltd. was adjusted to have a solid content of 5% by weight using toluene as a solvent to obtain a coating agent A.
• an addition reaction type silicone resin release agent trade name: LTC750A manufactured by Toray Dow Corning Silicone Co., Ltd., having a polysiloxane structure
• platinum catalyst Toray Dow Corning Silicone (Toray Dow Corning Silicone) 2 parts by weight of trade name SRX212
• Coating B 100 parts by weight of an alkenyl group-containing silicone release agent (having a polysiloxane structure) aqueous dispersion / 12 parts by weight of a Si—H group-containing silicone aqueous dispersion has nonionic properties as an alkyl resin, which will be described later.
• An aqueous dispersion of an acrylic resin (emulsifier: nonionic emulsifier) was mixed, diluted with water, and adjusted to a solid content concentration of 5% by weight to obtain a coating agent B.
• coating material a 50 parts by weight of acrylic resin, 50 parts by weight of methylol-type melamine cross-linking agent (“Nikalac (registered trademark)” MW12LF manufactured by Sanwa Chemical Co., Ltd.), and a solid content concentration of 8% by weight. was mixed and stirred with water to obtain a coating material a.
• methylol-type melamine cross-linking agent (“Nikalac (registered trademark)” MW12LF manufactured by Sanwa Chemical Co., Ltd.)
• coating material E 60 parts by weight of "Clear Lacquer (registered trademark)” manufactured by Washin Paint Co., Ltd. as a coating material containing nitrocellulose, and 20 parts by weight of Epicoat 828 manufactured by Mitsubishi Chemical Co., Ltd. as an epoxy resin, cured.
• a melamine resin (“Uban (registered trademark)” 2061 manufactured by Mitsui Chemicals Co., Ltd.)
• a catalyst light ester PM manufactured by Kyoei Chemical Co., Ltd.
• Example 1 Using the coating agent a, use FDN-010 (phthalocyanine vanadium, sublimation temperature 340 ° C.) manufactured by Yamada Chemical Co., Ltd. as an infrared absorber so that the concentration is 1% by weight based on the total solid content concentration of the coating agent. It was added and stirred to obtain a coating agent a-1. Further, PET-1 was vacuum-dried at 160 ° C. for 2 hours, then put into an extruder, melted at 280 ° C., and extruded through a die onto a casting drum having a surface temperature of 25 ° C. to prepare an unstretched sheet.
• FDN-010 phthalocyanine vanadium, sublimation temperature 340 ° C.
• the sheet was preheated by a heated roll group, then stretched 3.5 times in the longitudinal direction (MD direction) at a temperature of 90 ° C., and then cooled by a roll group at a temperature of 25 ° C. to form a uniaxially stretched film.
• MD direction longitudinal direction
• a roll group a temperature of 25 ° C.
• the temperature inside the tenter is 110 ° C. while grasping both ends of the film with clips.
• the film was stretched 4.0 times in the width direction (TD direction) perpendicular to the longitudinal direction. Further, subsequently, heat fixing was performed at a temperature of 230 ° C.
• the film was wound to obtain a film having a base material layer having a thickness of 30 ⁇ m and a layer having an infrared absorber having a thickness of 0.1 ⁇ m.
• a coating agent A is further applied to the surface of the layer of the obtained film having an infrared absorber, and the film is coated with a gravure coater so that the coating thickness after drying is 0.1 ⁇ m, and dried and cured at 100 ° C. for 20 seconds.
• a film in which the release layers were laminated was obtained. Each characteristic of such a film is shown in the table. It was a film having no problem in dielectric paste coating property and peelability.
• the removability of the release layer of the film was evaluated according to item F. That is, D.
• a laser marker MDX1500 manufactured by KEYENCE CORPORATION was used. Since the amount of Si element, which is a component of the release agent, is small and the contact angle with water is less than 90 °, the film has excellent removability of the release layer.
• Example 2-4, 16 A film was obtained in the same manner as in Example 1 except that the infrared absorber concentration and coating thickness of the infrared absorbing layer and the film thickness of the base material were changed as described in the table. Each characteristic is shown in the table.
• Example 2 the concentration of the infrared absorber was high, and in Example 3, the coating thickness of the layer containing the infrared absorber was thicker, so that the film was excellent in removability of the release layer.
• Example 4 the intensity of the laser beam was set to 10 W, but sufficient removability was obtained.
• Example 16 since the thickness of the base film was reduced, the peeling force of the dielectric paste was reduced, and the film was excellent in handleability.
• Example 5 Instead of the infrared absorber of Example 1, a carbon black (non-sublimable) aqueous dispersion (WD-CB2) manufactured by Daito Kasei Kogyo Co., Ltd. was used and added so as to have the concentration shown in the table. Obtained a film in the same manner as in Example 1. Each characteristic is shown in the table. The film of Example 5 did not show a clear peak (maximum value) in the wavelength band of 800 nm or more and 1200 nm or less, but had a high average absorbance of 800 nm or more and 1200 nm or less and was excellent in removability of the release layer. It was a film.
• WD-CB2 carbon black (non-sublimable) aqueous dispersion manufactured by Daito Kasei Kogyo Co., Ltd.
• Example 6 instead of the infrared absorber of Example 1, an infrared absorber FDN-003 (phthalocyanine copper complex, sublimation temperature 380 ° C.) manufactured by Yamada Chemical Co., Ltd. was used and added so as to have the concentration shown in the table. Obtained a film in the same manner as in Example 1. Each characteristic is shown in the table. Further, in order to remove the demolding layer, a pulse laser diode (L11348-307-05) manufactured by Hamamatsu Photonics was used as the laser device, and the laser apparatus was carried out by continuous waves. The removability of the release layer is shown in the table. It was a film having no problem in removing the release layer.
• FDN-003 phthalocyanine copper complex, sublimation temperature 380 ° C.
• Example 7 Instead of the infrared absorber of Example 1, the infrared absorber FDN-003 (phthalocyanine copper complex, sublimation temperature 380 ° C.) manufactured by Yamada Chemical Co., Ltd. and FDN-010 (phthalocyanine vanadium) manufactured by Yamada Chemical Co., Ltd. , Sublimation temperature (340 ° C.) was added so as to have a concentration of 1% by weight each, and a film was obtained in the same manner as in Example 1. Each characteristic is shown in the table. Further, in order to remove the demolding layer, MDX1500 and L11348-307-05 were used as the laser apparatus, and the laser apparatus was performed by continuous waves. The removability of the release layer is shown in the table. It was a film having no problem in removing the release layer.
• FDN-003 phthalocyanine copper complex, sublimation temperature 380 ° C.
• FDN-010 phthalocyanine vanadium
• PET-1 was vacuum-dried at 160 ° C. for 2 hours, then put into an extruder, melted at 280 ° C., and extruded through a die onto a casting drum having a surface temperature of 25 ° C. to prepare an unstretched sheet. Subsequently, the sheet was preheated by a heated roll group, then stretched 3.5 times in the longitudinal direction (MD direction) at a temperature of 90 ° C., and then cooled by a roll group at a temperature of 25 ° C. to form a uniaxially stretched film.
• MD direction longitudinal direction
• the coating material a-1 and the coating material B are applied so that the coating material a-1 is adjacent to the film and the coating material B is adjacent to the layer formed by the coating material a-1.
• the thickness after stretching and drying is adjusted to 0.1 ⁇ m by the die coating method, and the film is applied at the same time. While holding both ends of the film with clips, it is perpendicular to the longitudinal direction in the heating zone at a temperature of 110 ° C. in the tenter. It was stretched 4.0 times in the width direction (TD direction). Further, subsequently, heat fixing was performed at a temperature of 230 ° C. for 10 seconds in the heat treatment zone in the tenter.
• the film is wound to obtain a film having a base material layer having a thickness of 30 ⁇ m, a layer having an infrared absorber having a thickness of 0.1 ⁇ m, and a release layer having a thickness of 0.1 ⁇ m. It was.
• the removal of the release layer was carried out in the same manner as in Example 1. The characteristics of each and the removability of the release layer are shown in the table. It was a film having no problem in removing the release layer.
• Example 9 FDN-010 (phthalocyanine vanadium, sublimation temperature 340 ° C.) manufactured by Yamada Chemical Industry Co., Ltd. was added as an infrared absorber so as to have a concentration of 3% by weight with respect to the solid content concentration of the coating material A, and the mixture was stirred. A coating agent A-1 was obtained. Further, PET-1 was vacuum-dried at 160 ° C. for 2 hours, then put into an extruder, melted at 280 ° C., and extruded through a die onto a casting drum having a surface temperature of 25 ° C. to prepare an unstretched sheet.
• FDN-010 phthalocyanine vanadium, sublimation temperature 340 ° C.
• the sheet was preheated by a heated roll group, then stretched 3.5 times in the longitudinal direction (MD direction) at a temperature of 90 ° C., and then cooled by a roll group at a temperature of 25 ° C. to form a uniaxially stretched film.
• MD direction longitudinal direction
• a roll group a temperature of 25 ° C.
• the film was stretched 4.0 times in the width direction (TD direction) perpendicular to the longitudinal direction in the heating zone at a temperature of 110 ° C. in the tenter.
• heat fixing was performed at a temperature of 230 ° C. for 10 seconds in the heat treatment zone in the tenter.
• the film was wound to obtain a film having a thickness of 30 ⁇ m.
• the coating agent A-1 on one side of the obtained film, apply it with a gravure coater so that the coating thickness after drying becomes 0.1 ⁇ m, and dry and cure at 100 ° C. for 20 seconds to obtain an infrared absorber.
• a film was obtained by laminating layers having a release agent. Each characteristic is shown in the table.
• Example 2 Regarding the removability of the release layer, the same method as in Example 1 was carried out. Since the infrared absorber and the release agent are contained in the same layer, it was found that the film is easy to react and has excellent release properties.
• Example 10 a film was obtained in the same manner as in Example 9 except that the content of the infrared absorber was changed as shown in the table, and then the releasability was confirmed. Each characteristic is shown in the table. The amount of the infrared absorber added was large, and the film was excellent in removing the release layer.
• Example 11 The film of Example 10 was used, and the evaluation was performed in the same manner as in Example 10 except that the laser light intensity for removing the release layer was changed as shown in the table. The results are shown in the table. It was found that the amount of the infrared absorber added was large and the removability of the release layer was excellent even when the laser light intensity was lowered.
• Example 12 As the coating agent C-1, a coating agent was prepared by adding FDN-010 manufactured by Yamada Chemical Co., Ltd. so as to have a concentration of 1% by weight with respect to the solid content concentration of the coating agent C. Further, PET-1 was vacuum-dried at 160 ° C. for 2 hours, then put into an extruder, melted at 280 ° C., and extruded through a die onto a casting drum having a surface temperature of 25 ° C. to prepare an unstretched sheet.
• FDN-010 manufactured by Yamada Chemical Co., Ltd.
• the sheet was preheated by a heated roll group, then stretched 3.5 times in the longitudinal direction (MD direction) at a temperature of 90 ° C., and then cooled by a roll group at a temperature of 25 ° C. to form a uniaxially stretched film.
• MD direction longitudinal direction
• a roll group a temperature of 25 ° C.
• the film was stretched 4.0 times in the width direction (TD direction) perpendicular to the longitudinal direction in the heating zone at a temperature of 110 ° C. in the tenter.
• heat fixing was performed at a temperature of 230 ° C. for 10 seconds in the heat treatment zone in the tenter.
• the film was wound to obtain a film having a thickness of 30 ⁇ m.
• the coating agent C-1 on one side of the obtained film, apply it with a gravure coater so that the coating thickness after drying becomes 0.1 ⁇ m, and dry and cure at 100 ° C. for 20 seconds to obtain an infrared absorber.
• a film was obtained by laminating layers having a release agent. Each characteristic is shown in the table. It was found that the contact with water was rather large, and the number of repellents tended to increase slightly in the coatability of the dielectric paste.
• Example 9 the evaluation of the removability of the release layer was carried out in the same manner as in Example 9 except that the element concentration measurement by XPS in the item (F-1) was changed to fluorine, and the removability of the release layer was evaluated. It turned out that there was no problem.
• PET-B was vacuum-dried at 160 ° C. for 2 hours, then put into an extruder, melted at 280 ° C., and extruded through a die onto a casting drum having a surface temperature of 25 ° C. to prepare an unstretched sheet. Subsequently, the sheet was preheated by a heated roll group, then stretched 3.5 times in the longitudinal direction (MD direction) at a temperature of 90 ° C., and then cooled by a roll group at a temperature of 25 ° C. to form a uniaxially stretched film.
• MD direction longitudinal direction
• the film was stretched 4.0 times in the width direction (TD direction) perpendicular to the longitudinal direction in the heating zone at a temperature of 110 ° C. in the tenter. Further, subsequently, heat fixing was performed at a temperature of 230 ° C. for 10 seconds in the heat treatment zone in the tenter. Then, after slowly cooling uniformly in the cooling zone, the film was wound to obtain a film having an infrared absorber and having a thickness of 30 ⁇ m. A release layer is laminated on one side of the obtained film by applying the coating agent A with a gravure coater so that the coating thickness after drying becomes 0.1 ⁇ m, and drying and curing at 100 ° C. for 20 seconds.
• Example 9 Got the film. Each characteristic is shown in the table. Moreover, the evaluation of the removability of the release layer was carried out in the same manner as in Example 9. Since the polyester film, which is the base material layer, also contains an infrared absorber, it was found that the film is slightly inferior in the removability of the release layer because the laser light is absorbed by the entire Polysell film and the energy is dispersed. It was.
• Example 14 TF850H manufactured by Prime Polymer Co., Ltd. was put into an extruder as a polypropylene resin, melted at 240 ° C., and extruded through a die onto a casting drum having a surface temperature of 25 ° C. to prepare an unstretched sheet. Subsequently, the sheet was preheated by a heated roll group, stretched 4.3 times in the longitudinal direction (MD direction) at a temperature of 125 ° C., and then cooled by a roll group at a temperature of 25 ° C. to form a uniaxially stretched film.
• MD direction longitudinal direction
• the film was stretched 5.0 times in the width direction (TD direction) perpendicular to the longitudinal direction in the heating zone at a temperature of 160 ° C. in the tenter. Subsequently, heat fixation was performed in the heat treatment zone in the tenter at a temperature of 140 ° C. for 10 seconds. Then, after slowly cooling uniformly in the cooling zone, the film was wound to obtain a film having a thickness of 30 ⁇ m. On one side of the obtained film, a coating agent a-1 was used, applied with a bar coater so that the coating thickness after drying was 0.1 ⁇ m, and dried and cured at 100 ° C. for 60 seconds to form a substrate layer.
• a film obtained by laminating a layer having an infrared absorber having a thickness of 0.1 ⁇ m on a certain polypropylene film was obtained.
• a coating agent A is used on the surface of the layer of the obtained film having an infrared absorber, applied with a gravure coater so that the coating thickness after drying is 0.1 ⁇ m, and dried and cured at 100 ° C. for 20 seconds.
• a film in which a release layer was laminated was obtained. Each characteristic is shown in the table. Since the melting point is low, the film is inferior in handleability and slightly inferior in peelability of the dielectric, but there is no problem in practical use.
• the removability of the release layer was evaluated according to item F. That is, D.
• the green sheet prepared according to the above section was peeled off to a size of 10 cm ⁇ 10 cm, and the portion was irradiated with continuous wave laser light having a wavelength of 1064 nm and an intensity of 20 W, and then the residual layer of the release layer was subjected to the Si element content and water. It was evaluated by measuring the contact angle of.
• a laser marker MDX1500 manufactured by KEYENCE CORPORATION was used as the laser apparatus. Since the amount of Si element, which is a component of the release agent, is small and the contact angle with water is less than 90 °, the film has excellent removability of the release layer.
• Example 15 Apply the coating agent a-1 on one side of the polyphenylene sulfide (PPS) film "Trelina” (registered trademark) (30 ⁇ m) manufactured by Toray Industries, Inc., and apply it with a bar coater so that the coating thickness after drying is 0.1 ⁇ m. Then, it was dried and cured at 200 ° C. for 40 seconds to obtain a film in which a layer having an infrared absorber having a thickness of 0.1 ⁇ m was laminated on a PPS film as a base material layer.
• PPS polyphenylene sulfide
• a coating agent A is used on the surface of the layer of the obtained film having an infrared absorber, applied with a gravure coater so that the coating thickness after drying is 0.1 ⁇ m, and dried and cured at 100 ° C. for 20 seconds. Further, a film in which a release layer was laminated was obtained. Each characteristic is shown in the table. It was a film having no problem in dielectric paste coating property and peelability.
• the removability of the release layer was evaluated according to item F. That is, D.
• the green sheet prepared according to the above section was peeled off to a size of 10 cm ⁇ 10 cm, and the portion was irradiated with continuous wave laser light having a wavelength of 1064 nm and an intensity of 20 W, and then the residual layer of the release layer was subjected to the Si element content and water. It was evaluated by measuring the contact angle of.
• a laser marker MDX1500 manufactured by KEYENCE CORPORATION was used as the laser apparatus. Since the amount of Si element, which is a component of the release agent, is small and the contact angle with water is less than 90 °, the film has excellent removability of the release layer.
• PET-1 was vacuum-dried at 160 ° C. for 2 hours, then put into an extruder, melted at 280 ° C., and extruded through a die onto a casting drum having a surface temperature of 25 ° C. to prepare an unstretched sheet. Subsequently, the sheet was preheated by a heated roll group, then stretched 3.5 times in the longitudinal direction (MD direction) at a temperature of 90 ° C., and then cooled by a roll group at a temperature of 25 ° C. to form a uniaxially stretched film.
• MD direction longitudinal direction
• the film was stretched 4.0 times in the width direction (TD direction) perpendicular to the longitudinal direction in the heating zone at a temperature of 110 ° C. in the tenter. Further, subsequently, heat fixing was performed at a temperature of 230 ° C. for 10 seconds in the heat treatment zone in the tenter. Then, after slowly cooling uniformly in the cooling zone, the film was wound to obtain a film having a thickness of 30 ⁇ m.
• a coating agent D is used on one side of the obtained film, and the film is coated with a gravure coater so that the coating thickness after drying is 0.3 ⁇ m, and dried and cured at 100 ° C.
• Example 2 A film having an absorbing layer was obtained. Further, the release layer is applied by the gravure coating method using the coating agent A in the same manner as in Example 1 so as to be in contact with the layer that absorbs infrared rays of the film having the layer that absorbs infrared rays, and has the release layer. I got a film. Each characteristic is shown in the table. Regarding the release layer removability, the same method as in Example 1 was carried out.
• the film of Example 17 did not show a clear peak (maximum value) in the band of wavelength 800 nm or more and 1200 nm or less, but had a high average absorbance of wavelength 800 nm or more and 1200 nm or less, and the infrared absorber and the release agent were present. It was found that the film was contained in the same layer, so that the reaction proceeded easily and the release layer was excellent in removability.
• Example 18 and 19 In Examples 18 and 19, FDN-010 (phthalocyanine vanadium, sublimation temperature 340 ° C.) manufactured by Yamada Chemical Co., Ltd. was added to the coating material E as an infrared absorber as an infrared absorber as shown in the table. Instead of the coating material D of Example 17, the layer containing the infrared absorber and the release agent (release layer) was used in the same manner as in Example 17. Obtained a film to have. Each characteristic is shown in the table.
• FDN-010 phthalocyanine vanadium, sublimation temperature 340 ° C.
• Example 2 Regarding the removability of the release layer, the same method as in Example 1 was carried out. Since the infrared absorber and the release agent are contained in the same layer, it was found that the film is easy to proceed with the reaction and has excellent removability of the release layer.
• Example 20 In Example 20, a pulse wave laser was used instead of a continuous wave when removing the film releasability produced in Example 17. Specifically, a laser marker MDX1500 manufactured by KEYENCE CORPORATION was used as a laser apparatus, and laser light was oscillated and irradiated at a wavelength of 1064 nm, an output of 20 W, and a frequency of 200 kHz. Each characteristic is shown in the table. It was a film having excellent removability of the release layer.
• PET-1 was vacuum-dried at 160 ° C. for 2 hours, then put into an extruder, melted at 280 ° C., and extruded through a die onto a casting drum having a surface temperature of 25 ° C. to prepare an unstretched sheet. Subsequently, the sheet was preheated by a heated roll group, then stretched 3.5 times in the longitudinal direction (MD direction) at a temperature of 90 ° C., and then cooled by a roll group at a temperature of 25 ° C. to form a uniaxially stretched film.
• MD direction longitudinal direction
• the coating agent a is applied to the obtained uniaxially stretched film with a Meyer bar so that the thickness after stretching and drying is 0.1 ⁇ m, and then the temperature inside the tenter is 110 ° C. while grasping both ends of the film with clips.
• the film was stretched 4.0 times in the width direction (TD direction) perpendicular to the longitudinal direction.
• heat fixing was performed at a temperature of 230 ° C. for 10 seconds in the heat treatment zone in the tenter. Then, after slowly cooling uniformly in the cooling zone, the film was wound to obtain a film having a thickness of 30 ⁇ m.
• a release layer is laminated on one side of the obtained film by further applying the coating agent A with a gravure coater so that the coating thickness after drying becomes 0.1 ⁇ m, and drying and curing at 100 ° C. for 20 seconds. And got the film.
• Each characteristic is shown in the table. No absorption peak was obtained at a wavelength of 800 nm or more and 1200 nm or less, and the average absorbance at a wavelength of 800 nm or more and 1200 nm was also low.
• the removability of the release layer was evaluated in the same manner as in Example 1, but there was no layer containing an infrared absorber, no absorption peak was present at a wavelength of 800 nm or more and 1200 nm or less, and the wavelength was 800 nm or more. Since the film has a low average absorptivity at 1200 nm, the removability of the release layer was not excellent.
• PET-1 was vacuum-dried at 160 ° C. for 2 hours, then put into an extruder, melted at 280 ° C., and extruded through a die onto a casting drum having a surface temperature of 25 ° C. to prepare an unstretched sheet. Subsequently, the sheet was preheated by a heated roll group, then stretched 3.5 times in the longitudinal direction (MD direction) at a temperature of 90 ° C., and then cooled by a roll group at a temperature of 25 ° C. to form a uniaxially stretched film.
• MD direction longitudinal direction
• the film was stretched 4.0 times in the width direction (TD direction) perpendicular to the longitudinal direction in the heating zone at a temperature of 110 ° C. in the tenter. Further, subsequently, heat fixing was performed at a temperature of 230 ° C. for 10 seconds in the heat treatment zone in the tenter. Then, after slowly cooling uniformly in the cooling zone, the film was wound to obtain a film having a thickness of 30 ⁇ m. A release layer is laminated on one side of the obtained film by applying the coating agent A with a gravure coater so that the coating thickness after drying becomes 0.1 ⁇ m, and drying and curing at 100 ° C. for 20 seconds. , Got the film. Each characteristic is shown in the table. No absorption peak was obtained at a wavelength of 800 nm or more and 1200 nm or less, and the average absorbance at a wavelength of 800 nm or more and 1200 nm was also low.
• the removability of the release layer was evaluated in the same manner as in Example 1, but there was no layer containing an infrared absorber, no absorption peak was present at a wavelength of 800 nm or more and 1200 nm or less, and the wavelength was 800 nm or more. Since the film has a low average absorptivity at 1200 nm, the removability of the release layer was not excellent.
• PET-A was vacuum-dried at 160 ° C. for 2 hours, then put into an extruder, melted at 280 ° C., and extruded through a die onto a casting drum having a surface temperature of 25 ° C. to prepare an unstretched sheet. Subsequently, the sheet was preheated by a heated roll group, then stretched 3.5 times in the longitudinal direction (MD direction) at a temperature of 90 ° C., and then cooled by a roll group at a temperature of 25 ° C. to form a uniaxially stretched film.
• MD direction longitudinal direction
• the film was stretched 4.0 times in the width direction (TD direction) perpendicular to the longitudinal direction in the heating zone at a temperature of 110 ° C. in the tenter. Further, subsequently, heat fixing was performed at a temperature of 230 ° C. for 10 seconds in the heat treatment zone in the tenter. Then, after slowly cooling uniformly in the cooling zone, the film was wound to obtain a film having a thickness of 30 ⁇ m. A release layer is laminated on one side of the obtained film by applying the coating agent A with a gravure coater so that the coating thickness after drying becomes 0.1 ⁇ m, and drying and curing at 100 ° C. for 20 seconds. , Got the film.
• the film had a low content of the infrared absorber, could not obtain an absorption peak at a wavelength of 800 nm or more and 1200 nm or less, and had a low average absorbance at a wavelength of 800 nm or more and 1200 nm.
• the removability of the release layer was evaluated in the same manner as in Example 1, but the film had no absorption peak at a wavelength of 800 nm or more and 1200 nm or less, and had a low average absorbance at a wavelength of 800 nm or more and 1200 nm. Therefore, the removability of the release layer was not excellent.
• PET-C was vacuum dried at 160 ° C. for 2 hours, then put into an extruder, melted at 280 ° C., and extruded through a die onto a casting drum having a surface temperature of 25 ° C., but the amount containing an infrared absorber was large. , A sheet could not be obtained because the melt viscosity of the raw material was low.
• Comparative Example 5 A roll-shaped release film provided with a release layer produced in Comparative Example 2 was wound at a speed of 15 m / using a film feeding device, a winding device, and a cleaning brush provided in the middle. The release layer was peeled off while feeding out at min.
• a cleaning brush provided in the middle a stainless wire having a wire diameter of 0.1 mm and a bristles length of 15 mm, finished with an outer diameter of 180 mm was used.
• a hard chrome-plated free roll was used as the backup roll when the brush came into contact with the film.
• the film of the present invention is excellent in releasability, particularly excellent applicability and peelability of the dielectric paste, it can be suitably used as a film for a manufacturing process of a multilayer ceramic capacitor (MLCC). Further, since the release layer can be easily removed after the film of the present invention is used in the MLCC manufacturing process or the like, a recovery film from which the release layer has been removed can be easily produced.
• MLCC multilayer ceramic capacitor

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