JP4093419B2 - Foam sheet, manufacturing method and manufacturing apparatus thereof - Google Patents
Foam sheet, manufacturing method and manufacturing apparatus thereof Download PDFInfo
- Publication number
- JP4093419B2 JP4093419B2 JP2004224156A JP2004224156A JP4093419B2 JP 4093419 B2 JP4093419 B2 JP 4093419B2 JP 2004224156 A JP2004224156 A JP 2004224156A JP 2004224156 A JP2004224156 A JP 2004224156A JP 4093419 B2 JP4093419 B2 JP 4093419B2
- Authority
- JP
- Japan
- Prior art keywords
- sheet
- reflecting plate
- foamed
- light reflecting
- light
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
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- 238000004519 manufacturing process Methods 0.000 title claims description 27
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- 238000000034 method Methods 0.000 claims description 28
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- 239000007789 gas Substances 0.000 description 50
- 239000010410 layer Substances 0.000 description 44
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- 239000004973 liquid crystal related substance Substances 0.000 description 12
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- JHPBZFOKBAGZBL-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylprop-2-enoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)=C JHPBZFOKBAGZBL-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-N 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- UJTRCPVECIHPBG-UHFFFAOYSA-N 3-cyclohexylpyrrole-2,5-dione Chemical compound O=C1NC(=O)C(C2CCCCC2)=C1 UJTRCPVECIHPBG-UHFFFAOYSA-N 0.000 description 1
- IYMZEPRSPLASMS-UHFFFAOYSA-N 3-phenylpyrrole-2,5-dione Chemical compound O=C1NC(=O)C(C=2C=CC=CC=2)=C1 IYMZEPRSPLASMS-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
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- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
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- 239000004734 Polyphenylene sulfide Substances 0.000 description 1
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- 239000000654 additive Substances 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
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- 230000003796 beauty Effects 0.000 description 1
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- GCTPMLUUWLLESL-UHFFFAOYSA-N benzyl prop-2-enoate Chemical compound C=CC(=O)OCC1=CC=CC=C1 GCTPMLUUWLLESL-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
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- 239000001273 butane Substances 0.000 description 1
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- KBLWLMPSVYBVDK-UHFFFAOYSA-N cyclohexyl prop-2-enoate Chemical compound C=CC(=O)OC1CCCCC1 KBLWLMPSVYBVDK-UHFFFAOYSA-N 0.000 description 1
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- RYSQYJQRXZRRPH-UHFFFAOYSA-J tin(4+);dicarbonate Chemical compound [Sn+4].[O-]C([O-])=O.[O-]C([O-])=O RYSQYJQRXZRRPH-UHFFFAOYSA-J 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
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- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
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Images
Classifications
-
- 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
- B29C44/00—Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
- B29C44/34—Auxiliary operations
- B29C44/3442—Mixing, kneading or conveying the foamable material
- B29C44/3446—Feeding the blowing agent
-
- 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
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/22—After-treatment of expandable particles; Forming foamed products
-
- 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
- B29C44/00—Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
-
- 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
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/03—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
- B29C48/07—Flat, e.g. panels
- B29C48/08—Flat, e.g. panels flexible, e.g. films
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- 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
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/16—Articles comprising two or more components, e.g. co-extruded layers
- B29C48/18—Articles comprising two or more components, e.g. co-extruded layers the components being layers
-
- 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
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
-
- 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
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
- C08J9/12—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
-
- 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
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
- C08J9/12—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
- C08J9/122—Hydrogen, oxygen, CO2, nitrogen or noble gases
-
- 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
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/16—Articles comprising two or more components, e.g. co-extruded layers
- B29C48/18—Articles comprising two or more components, e.g. co-extruded layers the components being layers
- B29C48/21—Articles comprising two or more components, e.g. co-extruded layers the components being layers the layers being joined at their surfaces
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2105/00—Condition, form or state of moulded material or of the material to be shaped
- B29K2105/0079—Liquid crystals
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2105/00—Condition, form or state of moulded material or of the material to be shaped
- B29K2105/04—Condition, form or state of moulded material or of the material to be shaped cellular or porous
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2105/00—Condition, form or state of moulded material or of the material to be shaped
- B29K2105/25—Solid
- B29K2105/253—Preform
- B29K2105/256—Sheets, plates, blanks or films
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2995/00—Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
- B29K2995/0012—Properties of moulding materials, reinforcements, fillers, preformed parts or moulds having particular thermal properties
- B29K2995/0015—Insulating
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2995/00—Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
- B29K2995/0012—Properties of moulding materials, reinforcements, fillers, preformed parts or moulds having particular thermal properties
- B29K2995/0016—Non-flammable or resistant to heat
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- 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
- C08J2333/00—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 only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers
- C08J2333/04—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 only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters
- C08J2333/06—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 only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters of esters containing only carbon, hydrogen, and oxygen, the oxygen atom being present only as part of the carboxyl radical
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- Chemical Kinetics & Catalysis (AREA)
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- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Extrusion Moulding Of Plastics Or The Like (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
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- Laminated Bodies (AREA)
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Description
本発明は、発泡シートに関する。詳しくは、本発明は、光反射板、電池等のセパレーター材料、包装用材料、鋼板ラミネート用材料など、特に、液晶等の表示装置用バックライト機構に使用される面状光源用光反射板として好適に使用し得る発泡シート、その製造方法及びその製造における使用に適した装置、並びに該発泡シートを用いた光反射板及びディスプレイ装置に関する。 The present invention relates to a foam sheet. Specifically, the present invention is a light reflector for a planar light source used in a backlight mechanism for a display device such as a liquid crystal, such as a light reflector, separator materials for batteries, packaging materials, steel sheet laminate materials, etc. The present invention relates to a foam sheet that can be suitably used, a method for producing the foam sheet, a device suitable for use in the production, a light reflection plate using the foam sheet, and a display device.
近年、ノートパソコンやデスクトップパソコンのモニター、テレビ、携帯電話などのディスプレイ装置として、薄型化が可能な液晶等の表示装置が数多く用いられている。例えば液晶表示装置は、それ自体が発光体でないために、バックライトと呼ばれる面状光源を設置して裏側から光を照射することにより表示が可能となる。このバックライトは、画面全体を均一に照射させるため、サイドライト型若しくは直下型と呼ばれる面状光源の構造をとるのが通常である。特に、ノート型パソコン等は薄型・小型化が望まれるため、薄型の液晶ディスプレイが可能な用途には、通常、サイドライト型(即ち画面に対し側面から光を照射するタイプ)のバックライトが適用される(特許文献1、2参照)。一方、液晶テレビのような大画面用には、サイドライト方式では画面の高輝度化が望めないことから直下型ライト方式が採用されている。
2. Description of the Related Art In recent years, many display devices such as liquid crystals that can be made thin have been used as display devices for notebook personal computers and desktop personal computers, televisions, mobile phones, and the like. For example, since a liquid crystal display device itself is not a light emitter, display can be performed by installing a planar light source called a backlight and irradiating light from the back side. In order to uniformly illuminate the entire screen, this backlight usually has a planar light source structure called a side light type or a direct type. In particular, since notebook PCs are desired to be thin and small, a sidelight type backlight (ie, a type that irradiates light from the side of the screen) is usually used for applications that enable thin liquid crystal displays. (See
一般的に、サイドライト方式の場合、冷陰極線管を照明光源とし、導光板のエッジから導光板内部の面内で光を均一に伝播・拡散させ、更に導光板から液晶画面とは反対方向に拡散された光を液晶画面方向へ効率的に反射させるため、導光板の下には反射板が設けられる。一方、直下型ライト方式は、液晶画面の下部に冷陰極線管を並列に設けるものであって、反射板上に冷陰極線管が平行に並べられる。反射板としては、平面状、若しくは冷陰極線管の部分を半円凹状に成形したものなどが用いられる。 In general, in the case of the side light method, a cold cathode ray tube is used as an illumination light source, light is uniformly propagated and diffused from the edge of the light guide plate within the surface of the light guide plate, and further from the light guide plate in the opposite direction to the liquid crystal screen. In order to efficiently reflect the diffused light toward the liquid crystal screen, a reflecting plate is provided under the light guide plate. On the other hand, in the direct type light system, cold cathode ray tubes are provided in parallel at the lower part of the liquid crystal screen, and the cold cathode ray tubes are arranged in parallel on the reflector. As the reflection plate, a flat plate or a cold cathode ray tube part formed into a semicircular concave shape is used.
上記のように、液晶表示装置の画面全体を均一に照射するために反射板の果たす役割は大きい。この役割を満足させる反射板には、高度な反射特性が要求され、従来、内部に微細な気泡を含有させたフィルムや白色顔料を添加したフィルム等を、単独で、若しくはこれらのフィルムと金属板、プラスチック板などを張り合わせたものが使用されてきた。この反射板に使われるフィルムとしては、反射光における指向性が比較的小さい二軸延伸白色ポリエステルフィルムが多く用いられている。二軸延伸白色ポリエステルフィルムは、樹脂に充填剤を添加し、シート成形後延伸することにより微細な空隙を形成したものである。 As described above, the reflector plays a large role in uniformly irradiating the entire screen of the liquid crystal display device. Reflectors that satisfy this role are required to have a high degree of reflection characteristics. Conventionally, a film containing fine bubbles inside, a film added with a white pigment, etc., alone or with these films and a metal plate A laminate of plastic plates has been used. As a film used for this reflector, a biaxially stretched white polyester film having a relatively small directivity in reflected light is often used. The biaxially stretched white polyester film is formed by adding a filler to a resin and stretching after forming a sheet to form fine voids.
ところで、液晶ディスプレイ装置は、従来ノート型パソコンが主な用途であったが、近年ではそれに加えて、デスクトップ型パソコンやテレビ、携帯電話のディスプレイなど、様々な機器に採用が広がっている。また、より明るく鮮明な画像が求められており、高輝度、高精細な液晶画面を実現させるための改良が進められており、反射板に対する要求特性も更に厳しくなっている。このため、延伸白色ポリエステルフィルムの反射特性を向上させるための検討が、鋭意行われている(特許文献2、3参照)。
By the way, the liquid crystal display device has been mainly used for a notebook personal computer in the past, but in recent years, it has been increasingly used in various devices such as a desktop personal computer, a television, and a mobile phone display. Further, there is a demand for brighter and clearer images. Improvements for realizing a high-brightness and high-definition liquid crystal screen are being promoted, and the required characteristics for the reflector are becoming stricter. For this reason, studies for improving the reflection characteristics of the stretched white polyester film have been earnestly performed (see
しかし、延伸白色ポリエステルフィルムでは、反射特性を向上させるために気泡の数を増やそうとすると、ポリエステルに非相溶な樹脂や粒子の配合量を増す必要がある。このため、このような非相溶樹脂や粒子は、光を吸収してしまう不純物として、却って反射特性を低下させる原因となり、これ以上、反射特性の向上を望むことは困難である。また、延伸による気泡形成であるため、気泡のサイズがほぼ均一となり、その結果、特定の波長の光の反射率が低下する等の好ましくない現象が生じることがある。更に、直下型ライト方式のバックライトの場合、反射板に波形の成形加工が必要となるが、延伸された白色ポリエステルフィルムはその残留伸度が小さいため、このような成形加工には不向きである。 However, in the stretched white polyester film, in order to increase the number of bubbles in order to improve the reflection characteristics, it is necessary to increase the amount of resin or particles incompatible with the polyester. For this reason, such an incompatible resin or particle is an impurity that absorbs light and causes a decrease in the reflection characteristics, and it is difficult to further improve the reflection characteristics. In addition, since the bubbles are formed by stretching, the size of the bubbles becomes almost uniform, and as a result, an undesirable phenomenon such as a decrease in reflectance of light having a specific wavelength may occur. Furthermore, in the case of a direct light type backlight, a corrugated molding process is required on the reflector, but the stretched white polyester film has a small residual elongation and is not suitable for such a molding process. .
上記の延伸白色ポリエステルフィルムに替わるものとして、ロールを加圧不活性ガス中に保持しポリエステル樹脂シートに不活性ガスを含浸させた後、常圧下で加熱して発泡させて得たポリエステル樹脂発泡シート(特許文献4参照)が知られている(古河電気工業株式会社からMCPET(登録商標):エムシーペットの名称で入手可能)。
この方法により得られたポリエステル樹脂発泡シートは、不活性ガスの圧力が開放されたときの気泡発生メカニズムを利用するため、延伸による発泡のように、不純物を含んだり、気泡のサイズが完全に揃ったりすることがない。その結果、延伸白色ポリエステルフィルムと比較して反射特性を向上させることが可能となる。また延伸フィルムではないため、成形加工も容易である。
As an alternative to the above stretched white polyester film, a polyester resin foam sheet obtained by holding a roll in a pressurized inert gas and impregnating the polyester resin sheet with an inert gas and then heating and foaming under normal pressure. (See Patent Document 4) (MCPET (registered trademark): available from Furukawa Electric Co., Ltd.).
The polyester resin foam sheet obtained by this method uses a bubble generation mechanism when the pressure of the inert gas is released, so that it contains impurities or bubbles are completely aligned like foaming by stretching. There is nothing to do. As a result, it is possible to improve the reflection characteristics as compared with the stretched white polyester film. Moreover, since it is not a stretched film, a shaping | molding process is also easy.
このように、上記のポリエステル樹脂発泡シートは、延伸白色ポリエステルフィルムの欠点を補うものである。しかし、ポリエステル樹脂シートに不活性ガスを含浸させるのに時間がかかるため、生産性が良くない。また、シート表面で破泡が起こり易いため、表面が粗くなってしまう欠点がある。さらに、表面に無発泡の層を設けようとすれば、ポリエステル樹脂シートを発泡させた後に無発泡シートを貼り合わせる方法しかなく、反射特性に悪影響を及ぼしてしまう欠点もある。 Thus, said polyester resin foam sheet compensates the fault of a stretched white polyester film. However, since it takes time to impregnate the polyester resin sheet with an inert gas, productivity is not good. In addition, there is a drawback that the surface becomes rough because bubbles are easily broken on the surface of the sheet. Furthermore, if a non-foamed layer is to be provided on the surface, there is only a method of bonding the non-foamed sheet after foaming the polyester resin sheet, and there is a drawback in that the reflection characteristics are adversely affected.
一方、メタクリル酸メチル系重合体と発泡剤を押出機で溶融混練して円筒状の発泡体を得、次いで延伸・冷却し、切り開きシート状に引き取ることにより得られる発泡シートの製造方法が知られている(特許文献5参照)。また、シート形態の微細気泡ポリマー材料を押出しして積層物品を形成する方法が知られている(特許文献6参照)。しかし、これらの方法では、気泡の大きさをコントロールすることはできないため、気泡サイズが大きくなってしまい、反射特性の充分な向上は望めない。
特許文献6に開示された方法では、発泡シートと無発泡シートの積層体は、接着による積層が想定されている。しかし、接着による積層では、積層界面に境界ができてしまうため、界面での反射、屈折、更には光の吸収が起こってしまい、トータルの反射特性に悪影響が起こり易いという不都合が考えられる。
On the other hand, a method for producing a foamed sheet obtained by melting and kneading a methyl methacrylate polymer and a foaming agent with an extruder to obtain a cylindrical foam, then drawing and cooling, and taking up into a cut sheet is known. (See Patent Document 5). Further, a method of forming a laminated article by extruding a sheet-shaped fine cell polymer material is known (see Patent Document 6). However, in these methods, the size of the bubbles cannot be controlled, so that the size of the bubbles becomes large, and a sufficient improvement in reflection characteristics cannot be expected.
In the method disclosed in Patent Document 6, the laminated body of the foamed sheet and the non-foamed sheet is assumed to be laminated by adhesion. However, in the lamination by adhesion, a boundary is formed at the lamination interface, so that reflection, refraction, and light absorption at the interface occur, and the total reflection characteristics are likely to be adversely affected.
さらに、押出機内で樹脂組成物にガスを作用させて多孔質ないし発泡性のフィルムやシートを得る方法が知られている(特許文献7〜9参照)。しかし、特許文献7に開示された方法では、ポリマー中の不活性ガスの濃度を低く抑えても、気泡は大きくなっていくばかりであり、微細発泡による光反射板には使用できない。また、特許文献8に開示された方法によっても、一旦シート化した後のガスの放出により、シートの両面でガスの濃度にばらつきができてしまい、発泡する部分とあまり発泡しない部分が混在してしまうという不均一を生じる。更に、特許文献9に開示された方法では、延伸時に気泡サイズが大きく成長してしまう不都合が考えられる。
このように、発泡シートにおける気泡の大きさや形状の制御は、非常に重要であるにも関わらず困難であった。
Furthermore, a method of obtaining a porous or foamable film or sheet by causing a gas to act on the resin composition in an extruder is known (see Patent Documents 7 to 9). However, in the method disclosed in Patent Document 7, even if the concentration of the inert gas in the polymer is kept low, the bubbles only increase and cannot be used for a light reflecting plate by fine foaming. In addition, even by the method disclosed in Patent Document 8, the gas concentration after the sheet is once changed may cause variation in the gas concentration on both sides of the sheet, and the foaming part and the part that does not foam much are mixed. Cause non-uniformity. Furthermore, in the method disclosed in Patent Document 9, there is a disadvantage that the bubble size grows large during stretching.
As described above, it is difficult to control the size and shape of the bubbles in the foam sheet, although it is very important.
従って、上述した従来の二軸延伸白色ポリエステルフィルムの反射特性の限界と成形加工の困難性、さらには気泡のサイズ、形状を用途に応じて適正化し、生産性が良好で、表面が美麗で光反射板用として好適な微細発泡シートを開発すべき課題があった。 Therefore, the limitations of the reflection characteristics of the conventional biaxially stretched white polyester film described above, the difficulty of molding, and the size and shape of the bubbles are optimized according to the application, the productivity is good, the surface is beautiful and the light There was a problem to develop a fine foam sheet suitable for a reflector.
上記課題は、以下に記載する本発明によって解決される。
即ち、本発明は、熱可塑性樹脂を含んで成る無延伸の発泡シートであって、シート中に含まれる気泡のうち80%以上が0.1〜20μmの範囲の気泡径を有し、空隙率が20〜80%である発泡シートに関する。
また、本発明の別の態様では、気体を溶解させた熱可塑性樹脂の溶融ポリマーを無発泡状態でシート化する工程、シートを50〜200℃の温度条件下で真空に晒すことにより気泡を発生させる工程、を含む発泡シートの製造方法に関する。
本発明のさらに別の態様では、気体を溶解させた熱可塑性樹脂と、気体を溶解させない熱可塑性樹脂とを共押出しすることを特徴とする発泡シートの製造方法に関する。
The above problems are solved by the present invention described below.
That is, the present invention is an unstretched foamed sheet comprising a thermoplastic resin, and 80% or more of the bubbles contained in the sheet have a cell diameter in the range of 0.1 to 20 μm, and the porosity Relates to a foamed sheet of 20 to 80%.
In another aspect of the present invention, a step of forming a molten polymer of a thermoplastic resin in which a gas is dissolved in a non-foamed state, and generating bubbles by exposing the sheet to a vacuum under a temperature condition of 50 to 200 ° C. And a step of causing the foamed sheet to be produced.
In still another aspect of the present invention, the present invention relates to a method for producing a foam sheet, which comprises coextruding a thermoplastic resin in which a gas is dissolved and a thermoplastic resin in which a gas is not dissolved.
本発明のさらに別の態様では、スクリュー、シリンダー、およびシリンダーの温度調節機構を備えた押出機であって、該シリンダーの一部の内面に、該シリンダーの外部に設けた高圧気体供給ユニットから供給される気体を導入するためのノズルを備えていることを特徴とする、発泡シート製造用押出装置に関する。
また、本発明のさらに別の態様では、シート成形機のキャスティングロールおよび/またはキャスティングロール以降に、内部を減圧可能なチャンバーおよびシール機構を備えた真空チャンバー装置と、該真空チャンバー装置に付随する真空発生装置が配置されてなる発泡シート用製造装置に関する。
In still another aspect of the present invention, an extruder having a screw, a cylinder, and a temperature control mechanism for the cylinder is supplied from a high-pressure gas supply unit provided on the inner surface of a part of the cylinder, outside the cylinder. The present invention relates to an extrusion apparatus for producing a foam sheet, which is provided with a nozzle for introducing a gas to be produced.
In still another aspect of the present invention, a vacuum chamber apparatus having a chamber capable of reducing the pressure inside the casting roll and / or the casting roll of the sheet forming machine and a sealing mechanism, and a vacuum associated with the vacuum chamber apparatus. The present invention relates to a foam sheet manufacturing apparatus in which a generator is arranged.
本発明者は鋭意検討した結果、無延伸のキャストシートでありながら、0.1〜20μmの範囲にある微細な気泡を有し、かつ一定以上の気泡密度であるべく、気相占有率を表す空隙率が20〜80%の範囲内であると、光反射板等に用いるべき発泡シートとして、前記した従来の発泡シートにはない表面の美麗、易成形加工性、良好な生産性が得られることを見出した。 As a result of intensive studies, the present inventor shows a gas phase occupancy ratio so as to have fine bubbles in a range of 0.1 to 20 μm and a bubble density of a certain level or more while being an unstretched cast sheet. When the porosity is in the range of 20 to 80%, as a foam sheet to be used for a light reflecting plate or the like, the surface beauty, easy moldability, and good productivity that are not found in the conventional foam sheets can be obtained. I found out.
本発明の発泡シートは無延伸シートであるため、発泡シートを適用する用途に応じた成形加工が容易である。ここで無延伸であるとは、シートに配向を生じさせる目的で一軸または二軸に延伸することを行わないことを意味し、キャストやシート化に伴って生じる程度の延伸は許容される。
本発明による発泡シートは、シート中に含まれる気泡のうち80%以上が0.1〜20μmの範囲の気泡径を有しているため、良好な反射特性が得られる。シート中に含まれる気泡のうち80%以上が0.4μm〜8μmの範囲の気泡径を有していることが好ましい。気泡径が小さ過ぎる場合には、光干渉効果などを引き起こすため、十分な反射が得られない。逆に、気泡径が大き過ぎる場合には、界面数を一定量存在させるためにシートの厚みを大きくする必要が生じ、その結果、シートの機械的強度が弱くなったり、所望の膜厚より厚い設計が必要となるなど、実用に供しにくくなることがある。
また、従来の延伸シートでは気泡径が均一であったため、特定の波長の光の反射率が低下する等の不具合があったが、本発明の発泡シートでは、シート中に含まれる気泡径が正規分布を示すことが、良好な反射特性が得られる点で有利である。
Since the foamed sheet of the present invention is an unstretched sheet, it can be easily molded according to the application to which the foamed sheet is applied. Here, the term “non-stretched” means that uniaxial or biaxial stretching is not performed for the purpose of causing the sheet to be oriented, and stretching that occurs with casting or sheeting is allowed.
In the foamed sheet according to the present invention, 80% or more of the bubbles contained in the sheet have a bubble diameter in the range of 0.1 to 20 μm, so that good reflection characteristics can be obtained. It is preferable that 80% or more of the bubbles contained in the sheet have a bubble diameter in the range of 0.4 μm to 8 μm. When the bubble diameter is too small, a light interference effect or the like is caused, so that sufficient reflection cannot be obtained. On the other hand, if the bubble diameter is too large, it is necessary to increase the thickness of the sheet in order to have a certain number of interfaces, and as a result, the mechanical strength of the sheet becomes weak or thicker than the desired film thickness. It may be difficult to put it into practical use, such as when design is required.
Moreover, since the cell diameter was uniform in the conventional stretched sheet, there was a problem such as a decrease in the reflectance of light of a specific wavelength. However, in the foam sheet of the present invention, the cell diameter contained in the sheet was normal. The distribution is advantageous in that good reflection characteristics can be obtained.
本発明による発泡シートは、空隙率が20〜80%の範囲にあるため、良好な反射特性が得られる。空隙率は、発泡シートに含まれる気泡の密度に相当し、シートの気相占有率を表すが、シート及び用いる樹脂の密度とシート体積から、これを求めることができる。シートの空隙率は50〜70%であることが好ましい。これは気泡の形状が真球状を維持するためには、理論的な最大の空隙率は約70%であり、これを大きく超えると、気泡がつぶれてしまい、良好な反射特性を得ることができないからである。逆に、空隙率が低過ぎる場合には、気泡の密度が低くなり過ぎるため、所望の反射特性が得られない。 Since the foamed sheet according to the present invention has a porosity in the range of 20 to 80%, good reflection characteristics can be obtained. The porosity corresponds to the density of bubbles contained in the foamed sheet and represents the gas phase occupation ratio of the sheet, and can be determined from the density of the sheet and the resin used and the sheet volume. The porosity of the sheet is preferably 50 to 70%. In order to maintain the spherical shape of the bubble, the theoretical maximum porosity is about 70%, and if it exceeds this, the bubble collapses and good reflection characteristics cannot be obtained. Because. On the other hand, when the porosity is too low, the density of the bubbles becomes too low, so that desired reflection characteristics cannot be obtained.
発泡シートを直下型ライト方式のバックライトユニットに使われる反射板として用いる場合、発泡シートに100℃以上の成形温度で成形加工が施されるのが通常である。このような成形加工を容易とし、良好な反射特性を発現させるため、本発明による発泡シートは、100℃の雰囲気下で測定される引張破断伸度が100%以上であり、かつ100℃、100%伸度での引張応力が50MPa以下であることが好ましい。引張破断伸度は150%以上であることが好ましく、引張応力は0〜30MPa以下であることが好ましい。 When the foamed sheet is used as a reflector used in a direct light type backlight unit, the foamed sheet is usually molded at a molding temperature of 100 ° C. or more. In order to facilitate such molding processing and to exhibit good reflection characteristics, the foamed sheet according to the present invention has a tensile elongation at break of 100% or more measured in an atmosphere of 100 ° C., and 100 ° C., 100 The tensile stress at% elongation is preferably 50 MPa or less. The tensile elongation at break is preferably 150% or more, and the tensile stress is preferably 0 to 30 MPa or less.
本発明による発泡シートを構成する主たる熱可塑性樹脂は、微細な発泡を促すため、溶融張力の高い樹脂であることが好ましい。従って、溶融状態の流動性を示すメルトフローレート(ASTM D1238−98に準じる)が0.5〜44g/10分である熱可塑性樹脂が好ましく、溶融状態の流動性が1.4〜30g/10分の熱可塑性樹脂がより好ましい。熱可塑性樹脂の流動性は、ASTM D1238−98に記載された各種ポリマーに関する測定条件(温度、荷重等)に準じて決定し得る。 The main thermoplastic resin constituting the foamed sheet according to the present invention is preferably a resin having a high melt tension in order to promote fine foaming. Accordingly, a thermoplastic resin having a melt flow rate (according to ASTM D1238-98) showing fluidity in the molten state of 0.5 to 44 g / 10 minutes is preferable, and fluidity in the molten state is 1.4 to 30 g / 10. More preferable is a thermoplastic resin for a minute. The fluidity of the thermoplastic resin can be determined according to measurement conditions (temperature, load, etc.) relating to various polymers described in ASTM D1238-98.
本発明において使用し得る熱可塑性樹脂の具体例としては、例えば、アクリル樹脂、メタクリル樹脂、ポリオレフィン、ポリアミド、ポリエステル、ポリカーボネート、スチレン系樹脂、ポリエーテル、ポリウレタン、ポリフェニレンスルフィド、ポリエステルアミド、ポリエーテルエステル、ポリ塩化ビニル、変性ポリフェニレンエーテル、ポリアリレート、ポリサルホン、ポリイミド、ポリエーテルイミド、ポリアミドイミド、およびこれらを主たる成分とする共重合体、並びにこれらの混合物等を挙げることができるが、これらに限定されない。 Specific examples of the thermoplastic resin that can be used in the present invention include, for example, acrylic resins, methacrylic resins, polyolefins, polyamides, polyesters, polycarbonates, styrene resins, polyethers, polyurethanes, polyphenylene sulfides, polyester amides, polyether esters, Examples thereof include, but are not limited to, polyvinyl chloride, modified polyphenylene ether, polyarylate, polysulfone, polyimide, polyetherimide, polyamideimide, copolymers containing these as main components, and mixtures thereof.
とりわけ、本発明による発泡シートを構成する主たる熱可塑性樹脂としてアクリル樹脂及び/又はメタクリル樹脂を用いると、特に良好な微細発泡性、成形性が得られるため好ましく、また、樹脂そのものの透明度が高いため、結果的に気泡界面における反射も良好となる。更に、耐光性も優れており、原料樹脂も比較的安価に入手し得る。
このようなアクリル樹脂又はメタクリル樹脂の具体例としては、例えば、アクリル酸エステル又はメタクリル酸エステルの単独重合体或いはアクリル酸エステル又はメタクリル酸エステルを50重量%以上と、他の一種以上のビニル単量体との共重合体が挙げられ、なかでも、メタクリル酸エステルを50重量%以上と、他の一種以上のビニル単量体との共重合体が好ましく、とりわけ、メタクリル酸アルキルエステルを50重量%以上と、アクリル酸アルキルエステルを50重量%以下と、メタクリル酸アルキルエステル及びアクリル酸アルキルエステルの少なくとも一方と共重合可能なビニル単量体の一種以上を49重量%以下との共重合体が好ましい。共重合体に含まれるアクリル酸アルキルエステルは、0.1重量%〜40重量%であることが好ましく、1重量%〜15重量%であることがより好ましい。上記のアクリル樹脂又はメタクリル樹脂は、それぞれを単独で又はブレンドして使用してよい。
In particular, it is preferable to use an acrylic resin and / or methacrylic resin as the main thermoplastic resin constituting the foamed sheet according to the present invention, because particularly good fine foamability and moldability can be obtained, and the transparency of the resin itself is high. As a result, reflection at the bubble interface is also improved. Furthermore, the light resistance is also excellent, and the raw material resin can be obtained relatively inexpensively.
Specific examples of such acrylic resin or methacrylic resin include, for example, acrylic acid ester or methacrylic acid ester homopolymer or acrylic acid ester or methacrylic acid ester of 50% by weight or more, and one or more other vinyl monomers. Among them, a copolymer of 50% by weight or more of a methacrylic acid ester and one or more other vinyl monomers is preferable, and in particular, 50% by weight of a methacrylic acid alkyl ester is preferable. A copolymer of 50% by weight or less of the acrylic acid alkyl ester and 49% by weight or less of one or more vinyl monomers copolymerizable with at least one of the methacrylic acid alkyl ester and the acrylic acid alkyl ester is preferable. . The acrylic acid alkyl ester contained in the copolymer is preferably 0.1% by weight to 40% by weight, and more preferably 1% by weight to 15% by weight. The above acrylic resins or methacrylic resins may be used alone or in combination.
このようなアクリル酸エステルとしては、例えば、アクリル酸メチル、アクリル酸エチル、アクリル酸ブチル、アクリル酸シクロヘキシル、アクリル酸フェニル、アクリル酸ベンジル、アクリル酸2−エチルヘキシル、アクリル酸2−ヒドロキシエチル等を挙げることができ、とりわけ、アクリル酸メチル、アクリル酸エチルが好ましい。また、メタクリル酸エステルとしては、例えば、メタクリル酸メチル、メタクリル酸エチル、メタクリル酸ブチル、メタクリル酸シクロヘキシル、メタクリル酸フェニル、メタクリル酸ベンジル、メタクリル酸2−エチルヘキシル、メタクリル酸2−ヒドロキシエチル等を挙げることができ、とりわけ、メタクリル酸メチル、メタクリル酸エチルが好ましい。共重合可能な他のビニル単量体としては、上記のアクリル酸エステル又はメタクリル酸エステルのほか、例えば、アクリル酸、メタクリル酸などの不飽和酸類、スチレン、α−メチルスチレン、アクリロニトリル、メタクリロニトリル、無水マレイン酸、フェニルマレイミド、シクロヘキシルマレイミド等を挙げることができる。 Examples of such acrylates include methyl acrylate, ethyl acrylate, butyl acrylate, cyclohexyl acrylate, phenyl acrylate, benzyl acrylate, 2-ethylhexyl acrylate, 2-hydroxyethyl acrylate, and the like. In particular, methyl acrylate and ethyl acrylate are preferred. Examples of the methacrylic acid ester include methyl methacrylate, ethyl methacrylate, butyl methacrylate, cyclohexyl methacrylate, phenyl methacrylate, benzyl methacrylate, 2-ethylhexyl methacrylate, 2-hydroxyethyl methacrylate, and the like. In particular, methyl methacrylate and ethyl methacrylate are preferable. Other vinyl monomers that can be copolymerized include, in addition to the above acrylic ester or methacrylic ester, for example, unsaturated acids such as acrylic acid and methacrylic acid, styrene, α-methylstyrene, acrylonitrile, methacrylonitrile. , Maleic anhydride, phenylmaleimide, cyclohexylmaleimide and the like.
上記のアクリル樹脂又はメタクリル樹脂の重量平均分子量(Mw)は、4万〜40万であることが好ましく、さらに好ましくは6万〜30万である。Mwが小さ過ぎると得られる発泡シートの機械強度が十分でない場合があり、Mwが大き過ぎると溶融粘度が高くなり、押出性能が低下する場合がある。 The weight average molecular weight (Mw) of the acrylic resin or methacrylic resin is preferably 40,000 to 400,000, more preferably 60,000 to 300,000. When Mw is too small, the mechanical strength of the obtained foamed sheet may not be sufficient, and when Mw is too large, the melt viscosity increases and the extrusion performance may decrease.
更に、上記のアクリル樹脂又はメタクリル樹脂は、ゴム状重合体を含むものであってもよい。アクリル樹脂又はメタクリル樹脂へゴム状重合体を配合することにより、樹脂の粘性および靭性が向上するため、耐衝撃性の良好な発泡シートが得られる。 Further, the above acrylic resin or methacrylic resin may contain a rubber-like polymer. By blending the rubber-like polymer into the acrylic resin or methacrylic resin, the viscosity and toughness of the resin are improved, so that a foam sheet having good impact resistance can be obtained.
本発明における熱可塑性樹脂には、発泡シートの反射特性を損なわない範囲内で、少量の、好ましくは0〜3重量%の範囲で、結晶化核剤、結晶化促進剤、気泡化核剤、抗酸化剤、安定剤、加工助剤、可塑剤、帯電防止剤、耐衝撃助剤、発泡剤、充填剤、艶消剤、離型剤、難燃剤、紫外線吸収剤、紫外線防止剤、顔料、染料、滑剤、蛍光増白剤などの各種添加剤が配合されていてよい。 In the thermoplastic resin of the present invention, a small amount, preferably in the range of 0 to 3% by weight, within a range that does not impair the reflective properties of the foam sheet, Antioxidants, stabilizers, processing aids, plasticizers, antistatic agents, impact aids, foaming agents, fillers, matting agents, mold release agents, flame retardants, UV absorbers, UV inhibitors, pigments, Various additives such as dyes, lubricants, and optical brighteners may be blended.
このうち気泡化核剤として機能する無機微粒子としては、それ自体を核として孔を形成し得るものが好ましく、例えば炭酸カルシウム、炭酸マグネシウム、炭酸亜鉛、酸化チタン(アナターゼ型、ルチル型)、酸化亜鉛、硫酸バリウム、硫化亜鉛、塩基性炭酸錫、雲母チタン、酸化アンチモン、酸化マグネシウム、リン酸カルシウム、シリカ、アルミナ、マイカ、タルク、カオリンなどを用いることができる。これらの中で、400〜70Onmの可視光域において吸収の少ない炭酸カルシウム、硫酸バリウムを用いることが特に好ましい。可視光域に吸収があると、輝度が低下する問題が発生することがある。 Among these, as the fine inorganic particles functioning as a bubbling nucleating agent, those capable of forming pores by themselves are preferable, for example, calcium carbonate, magnesium carbonate, zinc carbonate, titanium oxide (anatase type, rutile type), zinc oxide. Barium sulfate, zinc sulfide, basic tin carbonate, mica titanium, antimony oxide, magnesium oxide, calcium phosphate, silica, alumina, mica, talc, kaolin and the like can be used. Among these, it is particularly preferable to use calcium carbonate and barium sulfate, which have low absorption in the visible light region of 400 to 70 Onm. If there is absorption in the visible light region, there may be a problem that the luminance decreases.
シート中に気泡を形成させるため、押出機内で熱可塑性樹脂中に溶解させる気体としては、例えば二酸化炭素、窒素、ブタン、ヘリウム、アルゴン等が挙げられる。その中でも二酸化炭素、窒素は、ガス透過率が低く、安価で安全に取り扱える点で好ましく、これらを単独で、或いは組み合わせて使用してもよい。 Examples of the gas dissolved in the thermoplastic resin in the extruder in order to form bubbles in the sheet include carbon dioxide, nitrogen, butane, helium, and argon. Among these, carbon dioxide and nitrogen are preferable because they have low gas permeability and can be handled safely at low cost, and these may be used alone or in combination.
本発明の発泡シートは、可視光範囲における反射率を85%以上、かつ全光線透過率を10%以下とすることが、表面が美麗で特に光反射板用に好適な発泡シートとして好ましい。 The foam sheet of the present invention preferably has a reflectance in the visible light range of 85% or more and a total light transmittance of 10% or less as a foam sheet particularly suitable for light reflectors because of its beautiful surface.
本発明による発泡シートは、少なくとも片面にエンボス柄が転写されていてよい。このようなエンボス加工は、表面に微細な模様を形成させたキャスティングロール上で熱可塑性樹脂シートに模様を転写させる方法、または無地のキャスティングロールでシート化された発泡シートを一旦ロール上に巻き取った後、改めて微細な模様を表面に持つカレンダー装置にかけてシートに模様を転写させる方法などにより行うことができる。微細な模様としては、光の反射を効率よく行うための、梨地模様、市松模様、半球状模様、山形模様、ピラミッド状模様、またはそれらの複合模様などが挙げられる。 The foam sheet according to the present invention may have an embossed pattern transferred on at least one side. Such embossing is performed by transferring a pattern onto a thermoplastic resin sheet on a casting roll having a fine pattern formed on the surface, or once winding a foam sheet formed into a plain casting roll onto the roll. After that, it can be carried out by a method of transferring the pattern onto the sheet again by using a calendar device having a fine pattern on the surface. Examples of the fine pattern include a satin pattern, a checkered pattern, a hemispherical pattern, a chevron pattern, a pyramid pattern, or a composite pattern thereof for efficiently reflecting light.
本発明による発泡シートの厚みは、20〜500μmであることが好ましく、35〜350μmがより好ましい。厚みが小さ過ぎる場合、シートの平坦性を確保することが困難となり、光反射板として用いた際に、明るさにムラが生じやすい。一方、厚みが大き過ぎると成形性が悪化する場合がある。 The thickness of the foamed sheet according to the present invention is preferably 20 to 500 μm, and more preferably 35 to 350 μm. If the thickness is too small, it becomes difficult to ensure the flatness of the sheet, and unevenness in brightness tends to occur when used as a light reflecting plate. On the other hand, if the thickness is too large, the moldability may deteriorate.
本発明による上記発泡シートは、使用目的に応じて、これを少なくとも1層配置してなる2層以上の積層シートとしてもよい。積層シートとする場合、その副層部/主層部の比率は1/200〜1/3が好ましく、1/50〜1/4がより好ましい。副層部/主層部/副層部の3層積層シート又は3層以上の積層シートである場合には、該比率は両副層部の合計/主層部で表される。積層シートには、上記発泡シートのほか、無発泡層を少なくとも1層配置されていてよい。本発明による発泡シートは、上記の主層部として積層シート中に配置することが好ましい。 The foamed sheet according to the present invention may be a laminated sheet having two or more layers formed by arranging at least one layer according to the purpose of use. In the case of a laminated sheet, the ratio of the sublayer portion / main layer portion is preferably 1/200 to 1/3, and more preferably 1/50 to 1/4. In the case of a sub-layer part / main layer part / sub-layer part three-layer laminated sheet or a laminated sheet of three or more layers, the ratio is expressed as the sum of both sub-layer parts / main layer part. In addition to the foamed sheet, at least one non-foamed layer may be disposed on the laminated sheet. The foamed sheet according to the present invention is preferably disposed in the laminated sheet as the main layer part.
本発明による積層シートは、共押出、押出ラミネーション、熱ラミネーション、コーティング、蒸着等により形成されたものであってよい。なかでも、共押出による積層シートが好ましい。このような積層シートは、例えば、発泡層用主押出機と無発泡層用の副押出機からのポリマーを、ダイス内のマニホールド部若しくはダイに入る前に設置されたフィードブロック部で合流させることにより形成し得る。この共押出積層シートは、接着剤層を設ける必要がないため、反射特性にとって有利であると同時に生産性も良好である。さらに好ましくは、主押出層と副押出層の主原料組成を同じくすることにより、例えば発泡部分と無発泡部分に境界がなくなるなど、主層と副層の境界面の影響を少なくすることができるため、特に光反射板として使用する場合に有利であり得る。 The laminated sheet according to the present invention may be formed by coextrusion, extrusion lamination, thermal lamination, coating, vapor deposition or the like. Especially, the lamination sheet by co-extrusion is preferable. In such a laminated sheet, for example, polymers from a foam layer main extruder and a non-foamed layer sub-extruder are joined together in a manifold part in a die or a feed block part installed before entering the die. Can be formed. Since this coextruded laminated sheet does not need to be provided with an adhesive layer, it is advantageous in terms of reflection characteristics and at the same time has good productivity. More preferably, by making the main raw material composition of the main extrusion layer and the sub-extrusion layer the same, the influence of the interface between the main layer and the sublayer can be reduced, for example, there is no boundary between the foamed portion and the non-foamed portion. Therefore, it can be advantageous particularly when used as a light reflecting plate.
また、この共押出積層シートは、主層(A層)と副層(B層)の2層構成だけでなく、(B層)(A層)(B層)の3層構成、さらには(B層)(A層)(B層)(A層)・・・・(B層)(A層)(B層)のような多層構成を有することも可能であり、厚み方向の気泡形成状態を容易にコントロールし得る点で非常に有効である。 Moreover, this co-extrusion laminated sheet has not only a two-layer structure of a main layer (A layer) and a sub-layer (B layer), but also a three-layer structure of (B layer) (A layer) (B layer), B layer) (A layer) (B layer) (A layer) ... (B layer) (A layer) (B layer) can also have a multi-layered structure, bubble formation state in the thickness direction It is very effective in that it can be controlled easily.
本発明の別の態様では、スクリュー、シリンダー、およびシリンダーの温度調節機構を備えた押出機であって、該シリンダーの一部の内面に、該シリンダーの外部に設けた高圧気体供給ユニットから供給される気体を導入するためのノズルを備えていることを特徴とする、発泡シート製造用押出装置に関する。かかる押出装置は、本発明による上記発泡シート又は積層シートの製造に適したものである。ここで、高圧とは、臨界点を超える状態となる圧力であることが好ましく、例えば押出ガス発泡に有利な炭酸ガスの場合、臨界点は温度31.1℃、圧力7.52MPaである。従って、高圧気体供給ユニットは、各種ガスをそれぞれの臨界点を超える状態で供給することが可能な装置であることが好ましい。 In another aspect of the present invention, the extruder includes a screw, a cylinder, and a temperature control mechanism for the cylinder, and is supplied to a part of the inner surface of the cylinder from a high-pressure gas supply unit provided outside the cylinder. The present invention relates to an extrusion apparatus for producing a foam sheet, which is provided with a nozzle for introducing a gas. Such an extrusion apparatus is suitable for manufacturing the foamed sheet or the laminated sheet according to the present invention. Here, the high pressure is preferably a pressure that exceeds the critical point. For example, in the case of carbon dioxide gas advantageous for extrusion gas foaming, the critical point is a temperature of 31.1 ° C. and a pressure of 7.52 MPa. Therefore, the high-pressure gas supply unit is preferably an apparatus capable of supplying various gases in a state exceeding their critical points.
本発明において使用可能な押出装置は、単軸押出機、二軸押出機、単軸押出機を連結したタンデム押出機、二軸押出機と単軸押出機を組み合わせたタンデム押出機のいずれでもよい。押出機のシリンダー部分は、加熱するためのヒーター、冷却するための空冷装置、水冷装置または油冷装置を含む温調装置を備え、これらは5〜10のブロックに分割して制御可能であることが好ましい。また、シリンダーは、温調制御部分と同じ区分にブロック化されていることが好ましい。スクリューは通常、主に原料樹脂をフィードするゾーンと、樹脂を溶融圧縮するゾーン、さらに圧縮混錬ゾーンに分かれる。スクリューのディメンジョン等は使用する樹脂により最適に設計される。 The extrusion apparatus that can be used in the present invention may be any of a single-screw extruder, a twin-screw extruder, a tandem extruder that connects single-screw extruders, and a tandem extruder that combines a twin-screw extruder and a single-screw extruder. . The cylinder part of the extruder is equipped with a heater for heating, an air cooling device for cooling, a temperature control device including a water cooling device or an oil cooling device, and these can be controlled in 5-10 blocks. Is preferred. The cylinder is preferably blocked in the same section as the temperature control portion. The screw is generally divided into a zone for mainly feeding a raw material resin, a zone for melting and compressing the resin, and a compression kneading zone. The dimensions of the screw are optimally designed according to the resin used.
上記の押出装置内部には、押出機内で溶融された樹脂に気体を溶解させるためのノズルが設置され、好ましくはスクリューディメンジョンの溶融圧縮ゾーンに配置される。具体的には、該ノズルは、溶融圧縮ゾーンに位置するシリンダーの1ブロック部分の内面に、外部に設けた高圧気体供給ユニットから供給される気体を導入するために設置される。
ノズルの形状は、シリンダーの1ブロック部分の内面に全周にわたり微細な孔、例えば気孔径30μm以下、気孔率25%以下を有する構造とすることが好ましく、具体的には、シリンダー内面に金属またはセラミックスで構成されたリング状の着脱可能なノズルを装着する。このようなリング状の金属は、金属パウダーまたは金属繊維を焼結させた材料で構成されることが好ましい。
A nozzle for dissolving a gas in the resin melted in the extruder is installed inside the extrusion apparatus, and is preferably disposed in a melt compression zone of a screw dimension. Specifically, the nozzle is installed on the inner surface of one block portion of the cylinder located in the melt compression zone in order to introduce gas supplied from a high-pressure gas supply unit provided outside.
The shape of the nozzle is preferably a structure having fine holes, for example, a pore diameter of 30 μm or less and a porosity of 25% or less, on the inner surface of one block portion of the cylinder. A ring-shaped removable nozzle made of ceramics is installed. Such a ring-shaped metal is preferably composed of a material obtained by sintering metal powder or metal fiber.
また、本発明のさらに別の態様では、シート成形機のキャスティングロールおよび/またはキャスティングロール以降に、内部を減圧可能なチャンバーおよびシール機構を備えた真空チャンバー装置と、該真空チャンバー装置に付随する真空発生装置が配置されてなる発泡シート用製造装置に関する。かかる製造装置は、本発明による上記発泡シート又は積層シートの製造に適したものである。
このような真空チャンバー装置は、所望の発泡シートを得るために、減圧可能なチャンバーの内部を30KPa以下に減圧することが可能であることが好ましい。
In still another aspect of the present invention, a vacuum chamber apparatus having a chamber capable of reducing the pressure inside the casting roll and / or the casting roll of the sheet forming machine and a sealing mechanism, and a vacuum associated with the vacuum chamber apparatus. The present invention relates to a foam sheet manufacturing apparatus in which a generator is arranged. Such a manufacturing apparatus is suitable for manufacturing the foamed sheet or laminated sheet according to the present invention.
In order to obtain a desired foamed sheet, it is preferable that such a vacuum chamber apparatus can reduce the pressure inside the depressurizable chamber to 30 KPa or less.
本発明において使用可能なシート成形機は、通常、樹脂を溶融させるための押出機、シート化するためのフラットダイ、シートを冷却するためのキャストロール、シートの引取り装置、巻取り装置から構成される。フラットダイはTダイが好ましく、ダイ内部で積層させるマルチマニホールドタイプや、ダイの直前で積層させるフィードブロック装置を備えるものも挙げられる。キャストロールは通常、温調機能を備えており、温調方法は、冷却水、温水、またはオイル等を循環させたものや、さらに誘導加熱方式と組み合わせる場合もある。シート引き取り装置は、キャストロールに引き続きロールの温調機能を持たせてもよく、また、厚み測定装置、欠点検出装置、帯電防止装置、コロナ処理やフレーム処理などの表面処理装置を備えることも可能である。巻取り装置はターレット機構、タッチロール機構、巻き替え機構、張力制御装置などを備えることもできる。 The sheet molding machine that can be used in the present invention usually comprises an extruder for melting resin, a flat die for forming a sheet, a cast roll for cooling the sheet, a sheet take-up device, and a winding device. Is done. The flat die is preferably a T die, and examples include a multi-manifold type that is laminated inside the die and a feed block device that is laminated immediately before the die. The cast roll usually has a temperature control function, and the temperature control method may be combined with a method in which cooling water, hot water, oil, or the like is circulated, or in addition to an induction heating method. The sheet take-up device may have a roll temperature control function following the cast roll, and may also be provided with a thickness measurement device, defect detection device, antistatic device, surface treatment device such as corona treatment and frame treatment. It is. The winding device can include a turret mechanism, a touch roll mechanism, a rewinding mechanism, a tension control device, and the like.
本発明において使用可能なチャンバー装置は、キャストロール若しくはキャストロールに続く、引き取り装置中のロール上方に、ロールの曲率に沿った断面を持ち、シートに合わせた幅のボックス状の装置であって、外部に設けた真空ポンプによって、チャンバー内部の空気を排気して減圧させ得るものである。チャンバーボックスは、真空を保持するためのシール機構を有し、必要に応じ、複数の部屋で構成されている。 The chamber apparatus usable in the present invention is a box-shaped apparatus having a cross section along the curvature of the roll above the roll in the take-up apparatus following the cast roll or the cast roll, and having a width corresponding to the sheet, The inside of the chamber can be evacuated and decompressed by a vacuum pump provided outside. The chamber box has a sealing mechanism for maintaining a vacuum, and includes a plurality of rooms as necessary.
本発明において使用可能なチャンバー装置に付属するシール機構は、シートの流れ方向に対して入り口側のインレットシール、出口のアウトレットシール、両側に配置されるサイドシールを含んで構成され、インレットシールおよびアウトレットシールには、ラビリンスシールタイプ、接触ローラー方式シールタイプ等を採用することができる。サイドシールとしては、ラビリンスシールタイプ、接触ガイドタイプ等を採用することができる。 A sealing mechanism attached to a chamber apparatus usable in the present invention includes an inlet-side inlet seal, an outlet outlet seal, and side seals arranged on both sides with respect to the sheet flow direction. As the seal, a labyrinth seal type, a contact roller type seal type, or the like can be adopted. As the side seal, a labyrinth seal type, a contact guide type, or the like can be adopted.
本発明による発泡シートの製造方法について、その好ましい具体例を以下に説明するが、本発明はこれらの具体例に限定されるものではない。
まず、必要に応じて、加熱及び/又は乾燥された原料となる熱可塑性樹脂チップを、それぞれ予め加熱された発泡押出可能な主押出機(A)、および、発泡を行わない副押出機(B)に供給する。主押出機(A)には、機外に置かれたガス供給装置によって、好ましくは超臨界条件以上の条件にて、ガスを供給する。主押出機(A)内部で、溶融した熱可塑性樹脂とガスを十分混錬し、熱可塑性樹脂中にガスを溶解させて押し出す。
Although the preferable specific example is demonstrated below about the manufacturing method of the foam sheet by this invention, this invention is not limited to these specific examples.
First, if necessary, a thermoplastic resin chip as a raw material that has been heated and / or dried is preheated into a main extruder (A) capable of foam extrusion and a sub-extruder (B) that does not perform foaming. ). The main extruder (A) is supplied with gas, preferably under supercritical conditions, by a gas supply apparatus placed outside the apparatus. Inside the main extruder (A), the molten thermoplastic resin and gas are sufficiently kneaded, and the gas is dissolved in the thermoplastic resin and extruded.
主押出機(A)から押し出されたポリマー(a)と副押出機(B)から押し出されたポリマー(b)を、フィードブロックにて(b)(a)(b)の3層となるように合流させた後、Tダイに供給してシート状に吐出させる。このとき、ポリマー(a)は、ガスは溶解しているが、発泡していない無発泡シート状態となるように、ガス供給量を調整する。 The polymer (a) extruded from the main extruder (A) and the polymer (b) extruded from the sub-extruder (B) are made into three layers (b) (a) (b) in the feed block. Are then fed to a T die and discharged into a sheet. At this time, in the polymer (a), the gas supply amount is adjusted so as to be in a non-foamed sheet state in which gas is dissolved but not foamed.
Tダイから吐出させたシートを、キャスティングロールに着地させて冷却させる。このとき、シートは通常、透明状態の均一なシートである。キャスティングロール上で所定の温度まで冷却した後、キャスティングロールに続く引き取りロールにシートを導入させる。次いで、引き取りロール上に設けた真空チャンバーにより、シートを真空状態に晒す。するとシートは微細な発泡を生じ、超白色のシートに変化する。その後、このシートを巻き取り機によって、ロール上に巻き取る。 The sheet discharged from the T die is landed on a casting roll and cooled. At this time, the sheet is usually a transparent uniform sheet. After cooling to a predetermined temperature on the casting roll, the sheet is introduced into a take-up roll following the casting roll. Next, the sheet is exposed to a vacuum state by a vacuum chamber provided on the take-up roll. Then, a sheet | seat produces a fine foam and changes to a super-white sheet | seat. Thereafter, the sheet is wound on a roll by a winder.
本発明による上記発泡シート又は積層シートは、気体が溶解した熱可塑性樹脂を押出すことにより発泡させる工程を含む方法により製造し得る。この場合、真空チャンバー装置を用いずに発泡を行ってよく、無発泡状態又は発泡状態のシートを真空チャンバー装置に通過させてもよい。
本発明はある態様において、気体を溶解させた熱可塑性樹脂の溶融ポリマーを無発泡状態で押出およびシート化する工程、シートを50〜200℃の温度条件下で真空に晒すことにより気泡を発生させる工程、を含む発泡シートの製造方法に関する。かかる製造方法は、本発明による上記発泡シート又は積層シートの製造に適したものであり、上記各工程は、連続していることが好ましい。ここで、温度条件は、70〜120℃であることがより好ましい。
The foamed sheet or laminated sheet according to the present invention can be produced by a method including a step of foaming by extruding a thermoplastic resin in which a gas is dissolved. In this case, foaming may be performed without using the vacuum chamber device, and a non-foamed or foamed sheet may be passed through the vacuum chamber device.
In one aspect, the present invention is a process in which a molten polymer of a thermoplastic resin in which a gas is dissolved is extruded and formed into a sheet, and bubbles are generated by exposing the sheet to a vacuum at a temperature of 50 to 200 ° C. The present invention relates to a method for producing a foam sheet including a process. Such a production method is suitable for production of the foamed sheet or laminated sheet according to the present invention, and the respective steps are preferably continuous. Here, the temperature condition is more preferably 70 to 120 ° C.
本発明において「無発泡状態でシート化する」とは、溶融樹脂ポリマーに気体を溶解させるが、ダイス部分で吐出させる際に発泡することの無い状態でシート化することであって、溶解させる気体の量を減らし、及び/又は吐出条件を制御することによって行い得る。この無発泡状態のシートは、ポリマー中に気体が溶解しているため、シートに減圧等の刺激を与えることにより、容易に発泡させることが可能である。
このシート化後の後発泡方法によれば、シートの温度や減圧等の条件を調整することにより、気泡の発生状態を容易にコントロールできるため、気泡サイズや気泡数を最適化し易い点で好ましい。
In the present invention, “to form a sheet in a non-foamed state” means that the gas is dissolved in the molten resin polymer, but is formed into a sheet without foaming when being discharged at the die portion, and the gas to be dissolved This can be done by reducing the amount and / or controlling the discharge conditions. Since the non-foamed sheet has a gas dissolved in the polymer, it can be easily foamed by applying a stimulus such as reduced pressure to the sheet.
The post-foaming method after forming into a sheet is preferable in that the bubble generation state can be easily controlled by adjusting the conditions such as the temperature of the sheet and the pressure reduction, and therefore the bubble size and the number of bubbles can be easily optimized.
本発明のある態様では、発泡シートは、気体を溶解させた熱可塑性樹脂と、気体を溶解させない熱可塑性樹脂とを共押出しすることにより製造され得る。かかる製造方法は、本発明による上記発泡シート又は積層シートの製造に適したものである。 In one embodiment of the present invention, the foam sheet can be produced by co-extrusion of a thermoplastic resin in which a gas is dissolved and a thermoplastic resin that does not dissolve the gas. Such a manufacturing method is suitable for manufacturing the foamed sheet or laminated sheet according to the present invention.
このように、本発明の発泡シートは、ガス供給押出に続くシート化装置、真空チャンバー装置を用いることにより得ることができる。従って、インラインで、反射特性、加工性、表面平滑性に優れたシートを生産性良く製造することが可能である。 Thus, the foamed sheet of the present invention can be obtained by using a sheeting apparatus and a vacuum chamber apparatus following gas supply extrusion. Therefore, it is possible to produce a sheet excellent in reflection characteristics, workability, and surface smoothness in-line with high productivity.
本発明による上記発泡シート又は積層シートは、光反射板として好適に使用し得る。このような光反射板は、上記発泡シート又は積層シートに成形加工が施されたものであってよい。
本発明における成型加工とは、温度調節した金型を用いて真空成形、圧空成形或いはプレス成形、またはカレンダー加工等を行うことによって成形体を得ることを意味する。
The foamed sheet or laminated sheet according to the present invention can be suitably used as a light reflecting plate. Such a light reflecting plate may be obtained by molding the foamed sheet or the laminated sheet.
The molding process in the present invention means that a molded body is obtained by performing vacuum molding, pressure molding, press molding, calendering, or the like using a temperature-controlled mold.
以下に本発明を実施例に基づき詳細に説明するが、本発明はかかる実施例に限定されるものではない。 The present invention will be described in detail below based on examples, but the present invention is not limited to such examples.
[評価方法]
1.反射率
反射率は、分光光度計U−3410((株)日立製作所製)に、φ60積分球130−0632((株)日立製作所製)および10℃傾斜スペーサーを取りつけた状態で、可視光範囲(380〜780nm)における反射率を発泡シート又は積層シートの両面について求め、高い方の値を反射率とした。
[Evaluation methods]
1. Reflectivity Reflectance is in the visible light range with a spectrophotometer U-3410 (manufactured by Hitachi, Ltd.) and a φ60 integrating sphere 130-0632 (manufactured by Hitachi, Ltd.) and a 10 ° C. inclined spacer attached. The reflectance at (380 to 780 nm) was determined for both sides of the foamed sheet or laminated sheet, and the higher value was taken as the reflectance.
2.空隙率
空隙率は、樹脂シート体積に対する気泡の体積の割合であり、シートの厚みと面積からサンプルの体積を求め、重量を測定して、次式を用いて空隙率とした。
空隙率(%)=(1−(重量/樹脂密度)/体積)×100
2. Porosity The porosity is the ratio of the volume of bubbles to the volume of the resin sheet. The volume of the sample was determined from the thickness and area of the sheet, the weight was measured, and the porosity was determined using the following formula.
Porosity (%) = (1− (weight / resin density) / volume) × 100
3.シート厚み
発泡シート又は積層シートの厚み測定に関しては、発泡シート又は積層シートの幅方向に、等間隔に10点の測定点を設け、厚みゲージ(teclock社製厚みゲージ)を用いて測定点の厚みを測定した後、各点の測定値の平均を発泡シートの厚みとした。
3. Sheet thickness For measuring the thickness of a foamed sheet or laminated sheet, 10 measurement points are provided at equal intervals in the width direction of the foamed sheet or laminated sheet, and the thickness of the measured point is measured using a thickness gauge (a thickness gauge manufactured by teclock). After measuring, the average of the measured values at each point was taken as the thickness of the foamed sheet.
4.全光線透過率
全光線透過率は、JIS K7105:1981に準じて発泡シート及び積層シートについて評価した。
4). Total light transmittance The total light transmittance was evaluated for the foamed sheet and the laminated sheet according to JIS K7105: 1981.
5.引張破断伸度
引張破断伸度は、(株)オリエンテック製テンシロンUCT−100引張試験機を用いて、10mm幅、100mm長さのシートを100℃雰囲気下で5分間保持した後、300mm/分で伸長させた際のシート長手方向および横方向の破断伸度の平均値である。
5. Tensile elongation at break The tensile elongation at break is 300 mm / min after holding a 10 mm wide, 100 mm long sheet in a 100 ° C. atmosphere for 5 minutes using a Tensilon UCT-100 tensile tester manufactured by Orientec Co., Ltd. It is an average value of the breaking elongation in the longitudinal direction and the transverse direction when the sheet is stretched by.
6.引張応力
引張応力は、(株)オリエンテック製テンシロンUCT−100引張試験機を用いて、10mm幅、100mm長さのシートを100℃雰囲気下で5分間保持した後、300mm/分で伸長させた際のシート長手方向および横方向の100%伸度時点での応力値の平均値である。
6). Tensile stress Tensile stress was stretched at 300 mm / min after holding a sheet of 10 mm width and 100 mm length in a 100 ° C. atmosphere for 5 minutes using a Tensilon UCT-100 tensile tester manufactured by Orientec Co., Ltd. It is an average value of stress values at the time of 100% elongation in the longitudinal direction and lateral direction of the sheet.
[実施例1]
光学用アクリル樹脂(住友化学(株)スミペックスMGSS)を予め120℃の条件で4時間加熱したものを原料とし、これを1段目として35mm、L/Dが34の単軸押出機、2段目として50mm、L/Dが28の単軸押出機のタンデム構成押出機に供給し、さらに押出機の機外に設置した高圧ガス供給装置から、超臨界条件を越える38℃、15MPaにて、炭酸ガスを1段目押出機の溶融圧縮部のシリンダ部に設けたノズルに供給し、樹脂中に溶解、混錬させた。このときの炭酸ガスの供給量は、押出機の吐出量14.7kg/hに対して、炭酸ガスの割合を0.38kg/hとした。このときの押出温度は、1段目240℃、2段目200℃であった。
これをスリット幅150mm、スリット間隙0.8mmのダイから吐出させてシート化したところ、平均厚み230μm、88mm幅の白色発泡シートが得られた。
このシートをミクロトームにてフィルム断面を潰すことなく切断し、切断した断面を走査型電子顕微鏡S−2100A型((株)日立製作所製)を用いて、500倍にて観察したところ、気泡径は中心が14μmで気泡の80%以上が20μm以下の範囲の気泡径を有していた。気泡による空隙率は密度から計算して76%であった。
表面の荒れている部分を削り取った後、このシートの可視光範囲の反射率を測定したところ85%で、かつ全光線透過率は6%であった。
さらにフィルム強伸度自動測定装置(オリエンテック(株)製テンシロンAMF/RTA−100)を用い、試料サイズ:幅10mm×試長間100mm、温度100℃、引張速度:300mm/分の条件で測定したところ、引張破断伸度は141%、100℃、100%伸度における引張応力は12.0MPaであった。念のため、簡易成形テストを実施したところ、成形性は良好であった。
[Example 1]
Optical acrylic resin (Sumitomo Chemical Co., Ltd. Sumipex MGSS) heated in advance at 120 ° C for 4 hours is used as a raw material. This is the first stage, 35mm, L / D is 34 single screw extruder, 2 stages 50 mm, L / D is supplied to a tandem configuration extruder of 28 single screw extruder, and further from a high pressure gas supply device installed outside the extruder at 38 ° C. and 15 MPa exceeding the supercritical condition, Carbon dioxide gas was supplied to a nozzle provided in the cylinder part of the melt compression part of the first stage extruder, and dissolved and kneaded in the resin. At this time, the supply amount of carbon dioxide gas was 0.38 kg / h with respect to the discharge amount of the extruder 14.7 kg / h. The extrusion temperature at this time was 240 ° C. for the first stage and 200 ° C. for the second stage.
When this was discharged from a die having a slit width of 150 mm and a slit gap of 0.8 mm to form a sheet, a white foam sheet having an average thickness of 230 μm and a width of 88 mm was obtained.
This sheet was cut with a microtome without crushing the film cross section, and the cut cross section was observed at 500 times using a scanning electron microscope S-2100A type (manufactured by Hitachi, Ltd.). The center was 14 μm, and 80% or more of the bubbles had a bubble diameter in the range of 20 μm or less. The porosity due to bubbles was 76% calculated from the density.
After shaving off the rough surface, the reflectance of this sheet in the visible light range was measured and found to be 85% and the total light transmittance was 6%.
Furthermore, using a film strength and elongation automatic measuring device (Tensilon AMF / RTA-100 manufactured by Orientec Co., Ltd.), sample size: width 10 mm × sample length 100 mm, temperature 100 ° C., tensile speed: 300 mm / min. When measured, the tensile elongation at break was 141%, 100 ° C., and the tensile stress at 100% elongation was 12.0 MPa. As a precaution, when a simple molding test was performed, the moldability was good.
[実施例2]
押出機の吐出量を14.3kg/hとしたことと、炭酸ガスを0.03kg/hの割合で供給したこと以外は、実施例1と同様にしてシート化を行ったところ、透明の平滑なシートが得られた。このシートを90℃に加熱しながら、デシケーター(真空容器)に入れて28kPaに減圧したところ、発泡し白濁した。
この得られた白色シート(平均厚み:205μm)を実施例1と同様の方法で観察したところ、気泡径は中心が10μmで気泡の85%以上が20μm以下の範囲の気泡径を有していた。また空隙率は56%であった。このシートの可視光範囲の反射率は88%、かつ全光線透過率は7%であった。表面状態は多少荒れていたが、反射率の低下には至らなかった。
100℃における引張破断伸度は195%、100℃、100%伸度における引張応力は12.5MPaであった。
[Example 2]
Except that the discharge rate of the extruder was 14.3 kg / h, and carbon dioxide gas was supplied at a rate of 0.03 kg / h, sheeting was performed in the same manner as in Example 1 to obtain a transparent smooth A sheet was obtained. When this sheet was heated to 90 ° C. and placed in a desiccator (vacuum container) and depressurized to 28 kPa, it foamed and became cloudy.
When the obtained white sheet (average thickness: 205 μm) was observed in the same manner as in Example 1, the cell diameter was 10 μm at the center and 85% or more of the bubbles had a cell diameter in the range of 20 μm or less. . The porosity was 56%. The sheet had a reflectance in the visible light range of 88% and a total light transmittance of 7%. The surface condition was somewhat rough, but the reflectance did not decrease.
The tensile elongation at break at 100 ° C. was 195%, and the tensile stress at 100 ° C. and 100% elongation was 12.5 MPa.
[実施例3]
実施例2と同様の方法で得られた透明なシートを、50℃に加熱しながら、デシケーターに入れて28kPaに減圧した。
その結果得られた発泡シートは気泡サイズが小さくなり、気泡径は中心が7μmで気泡の100%が20μm以下の範囲の気泡径を有していた。また空隙率は32%であった。このシートの可視光範囲の反射率は89%、かつ全光線透過率は10%であった。表面状態は問題なかった。
[Example 3]
The transparent sheet obtained by the same method as in Example 2 was put in a desiccator while being heated to 50 ° C., and the pressure was reduced to 28 kPa.
As a result, the obtained foamed sheet had a reduced bubble size, and the bubble diameter was 7 μm at the center and 100% of the bubbles had a bubble diameter in the range of 20 μm or less. The porosity was 32%. This sheet had a reflectance in the visible light range of 89% and a total light transmittance of 10%. There was no problem with the surface condition.
[実施例4]
実施例2と同様の方法で得られた透明なシートを、今度は140℃に加熱しながら、デシケーターに入れて28kPaに減圧した。
その結果得られた発泡シートは気泡サイズが大きくなると共に、バラツキが大きくなった。気泡径は中心が18μmで気泡の80%が20μm以下の範囲の気泡径を有していた。また空隙率は61%であった。このシートの可視光範囲の反射率は86%、かつ全光線透過率は9%であった。表面には所々破泡した痕跡があった。
[Example 4]
The transparent sheet obtained by the same method as in Example 2 was placed in a desiccator while being heated to 140 ° C., and the pressure was reduced to 28 kPa.
As a result, the obtained foamed sheet increased in bubble size and variation. The bubble diameter was 18 μm at the center and 80% of the bubbles had a bubble diameter in the range of 20 μm or less. The porosity was 61%. The sheet had a reflectance in the visible light range of 86% and a total light transmittance of 9%. There were traces of broken bubbles on the surface.
[実施例5]
主押出機を用いて実施例1と同様の材料、装置、運転条件にて2段で押出しを行い(A層)、さらに副押出機として45mm、L/Dが34の単軸押出機を用いて、主押出機と同じ樹脂(住友化学(株)スミペックスMGSS)を炭酸ガスの供給を行わないで押出しして(B層)、ダイ直前に設置したフィードブロックにて、両者を共押出により(B層)/(A層)/(B層)の3層構成に積層させ、実施例2と同様にシート化した。さらに実施例2と同様にしてデシケーター中で減圧に晒し、発泡させた。
得られた白色積層シート(平均厚み:245μm)は、実施例2と異なり表面が非常に滑らかであった。実施例1と同様の方法で観察したところ、気泡径は中心が8μmで気泡の90%が20μm以下の範囲の気泡径を有していた。また空隙率は50%であった。このシートの可視光範囲の反射率は89%、かつ全光線透過率は9%であった。
100℃における引張破断伸度は163%、100℃、100%伸度における引張応力は13.3MPaであった。
[Example 5]
Extrusion was performed in two stages using the same materials, equipment and operating conditions as in Example 1 using the main extruder (A layer), and a single-screw extruder of 45 mm and L / D of 34 was used as the sub-extruder. The same resin as the main extruder (Sumitomo Chemical Co., Ltd. Sumipex MGSS) was extruded without supplying carbon dioxide (layer B), and both were co-extruded in a feed block installed immediately before the die ( B layers) / (A layers) / (B layers) were laminated into a three-layer structure and formed into a sheet in the same manner as in Example 2. Furthermore, it was exposed to reduced pressure in a desiccator and foamed in the same manner as in Example 2.
Unlike the Example 2, the obtained white laminated sheet (average thickness: 245 μm) had a very smooth surface. When observed by the same method as in Example 1, the bubble diameter was 8 μm at the center and 90% of the bubbles had a bubble diameter in the range of 20 μm or less. The porosity was 50%. The sheet had a reflectance in the visible light range of 89% and a total light transmittance of 9%.
The tensile elongation at break at 100 ° C. was 163%, and the tensile stress at 100 ° C. and 100% elongation was 13.3 MPa.
[比較例1]
炭酸ガスを0.6kg/hに増量したこと以外は実施例1と同様にして、シート化を行い、白色発泡シートを得た。しかし、ダイ直後でしばしば破泡して爆発音が起こった。またシート表面に波打ち現象が見られ、空隙率も85%に増加した。
[Comparative Example 1]
A white foamed sheet was obtained in the same manner as in Example 1 except that the amount of carbon dioxide was increased to 0.6 kg / h. However, there were frequent bubbles immediately after the die and explosions occurred. Further, a wave phenomenon was observed on the sheet surface, and the porosity increased to 85%.
[比較例2]
炭酸ガスを0.1kg/hに減量したこと以外は実施例1と同様にして、シート化を行ったところ、半透明のシートとなった。気泡径は20〜100μmの範囲に分布しており、なかでも50μm以上の大きな気泡が50%以上を占めていた。
[Comparative Example 2]
When a sheet was formed in the same manner as in Example 1 except that the amount of carbon dioxide gas was reduced to 0.1 kg / h, a translucent sheet was obtained. The bubble diameter was distributed in the range of 20 to 100 μm, and large bubbles of 50 μm or more occupied 50% or more.
[比較例3]
炭酸ガスを0.05kg/hに更に減量したこと以外は実施例1と同様にして、シート化を行ったところ、ほぼ透明のシートとなった。しかし、ところどころで2mm以上の大きさの気泡が不定期に出現した。
[Comparative Example 3]
When a sheet was formed in the same manner as in Example 1 except that the amount of carbon dioxide was further reduced to 0.05 kg / h, a substantially transparent sheet was obtained. However, in some places, bubbles with a size of 2 mm or more appeared irregularly.
[比較例4]
炭酸ガスを供給しなかったこと以外は実施例1と同様にして、シート化を行ったところ、透明のシートが得られた。このシートを、実施例2と同様にしてデシケーターで減圧したが、気泡の発生は認められなかった。
[Comparative Example 4]
When a sheet was formed in the same manner as in Example 1 except that carbon dioxide was not supplied, a transparent sheet was obtained. The sheet was decompressed with a desiccator in the same manner as in Example 2, but no generation of bubbles was observed.
[比較例5]
実施例2で得られた透明未発泡シートを、40℃に加熱しながらデシケーターに入れて減圧したが、気泡の発生は認められなかった。
[比較例6]
実施例2で得られた透明未発泡シートを、210℃に加熱しながらデシケーターに入れて減圧したところ、所々表面が風船のように発泡してしまった。
[比較例7]
実施例2で得られた透明未発泡シートを、実施例2と同様に90℃に加熱しながらデシケーターに入れて減圧し、さらに該状態で1時間放置した。得られたシートは実施例2で得られたシートより気泡が大きく成長しており、気泡径は中心が30μmで気泡の60%が20μm以下の範囲の気泡径を有していた。このシートの可視光範囲の反射率は75%、かつ全光線透過率は6%であった。
[Comparative Example 5]
The transparent unfoamed sheet obtained in Example 2 was placed in a desiccator while being heated to 40 ° C. and decompressed, but no generation of bubbles was observed.
[Comparative Example 6]
When the transparent unfoamed sheet obtained in Example 2 was put into a desiccator while being heated to 210 ° C. and depressurized, the surface was foamed like a balloon in some places.
[Comparative Example 7]
The transparent unfoamed sheet obtained in Example 2 was put into a desiccator while being heated to 90 ° C. in the same manner as in Example 2, and the pressure was reduced. The obtained sheet had larger bubbles growing than the sheet obtained in Example 2, and the bubble diameter was 30 μm at the center and 60% of the bubbles had a bubble diameter of 20 μm or less. This sheet had a reflectance in the visible light range of 75% and a total light transmittance of 6%.
本発明の発泡シートは、その白色性、耐候性、保温性、絶縁性、微細気泡含有性などから、反射板、包装用材料、鋼板ラミネート用材料、セパレーター材料等に適用可能であるが、その適用範囲はこれらに限られるものではない。本発明の発泡シートは、液晶表示装置のバックライト機構に使用される面状光源用光反射板として、特に好適に使用できる。
本発明の主たる態様および好ましい態様は、以下を包含する。
〔1〕熱可塑性樹脂を含んで成る無延伸の発泡シートであって、シート中に含まれる気泡のうち80%以上が0.1〜20μmの範囲の気泡径を有し、空隙率が20〜80%である発泡シート。
〔2〕100℃の雰囲気下で測定される引張破断伸度が100%以上であり、かつ100℃、100%伸度での引張応力が50MPa以下である上記〔1〕記載の発泡シート。
〔3〕熱可塑性樹脂は、溶融状態の流動性(ASTM D1238−98に準じる)が0.5〜44g/10分である上記〔1〕または〔2〕に記載の発泡シート。
〔4〕熱可塑性樹脂は、アクリル樹脂及び/又はメタクリル樹脂である上記〔1〕〜〔3〕のいずれかに記載の発泡シート。
〔5〕核剤を0〜3重量%含む上記〔1〕〜〔4〕のいずれかに記載の発泡シート。
〔6〕少なくとも片面にエンボス柄が転写されている、上記〔1〕〜〔5〕のいずれかに記載の発泡シート。
〔7〕2層以上の積層シートであって、上記〔1〕〜〔6〕のいずれかに記載の発泡シートが少なくとも1層配置されてなる積層シート。
〔8〕無発泡層が少なくとも1層配置されてなる上記〔7〕記載の積層シート。
〔9〕可視光範囲における反射率が85%以上で、かつ全光線透過率が10%以下である上記〔1〕〜〔8〕のいずれかに記載のシート。
〔10〕上記〔1〕〜〔9〕のいずれかに記載のシートを用いた光反射板。
〔11〕上記〔10〕に記載のシートに成形加工が施されている光反射板。
〔12〕上記〔10〕又は〔11〕に記載の光反射板を用いたディスプレイ装置。
〔13〕気体が溶解した熱可塑性樹脂を押出すことにより発泡させる工程を含む上記〔1〕〜〔9〕のいずれかに記載のシートの製造方法。
〔14〕気体を溶解させた熱可塑性樹脂の溶融ポリマーを無発泡状態でシート化する工程、
シートを50〜200℃の温度条件下で真空に晒すことにより気泡を発生させる工程、
を含む発泡シートの製造方法。
〔15〕気体を溶解させた熱可塑性樹脂の溶融ポリマーを無発泡状態でシート化する工程、
シートを50〜200℃の温度条件下で真空に晒すことにより気泡を発生させる工程、
を含む上記〔1〕〜〔9〕のいずれかに記載のシートの製造方法。
〔16〕気体を溶解させた熱可塑性樹脂と、気体を溶解させない熱可塑性樹脂とを共押出しすることを特徴とする上記〔1〕〜〔9〕、〔13〕〜〔15〕のいずれかに記載のシートの製造方法。
〔17〕スクリュー、シリンダー、およびシリンダーの温度調節機構を備えた押出機であって、該シリンダーの一部の内面に、該シリンダーの外部に設けた高圧気体供給ユニットから供給される気体を導入するためのノズルを備えていることを特徴とする、発泡シート製造用押出装置。
〔18〕スクリュー、シリンダー、およびシリンダーの温度調節機構を備えた押出機であって、該シリンダーの一部の内面に、該シリンダーの外部に設けた高圧気体供給ユニットから供給される気体を導入するためのノズルを備えていることを特徴とする、上記〔1〕〜〔9〕のいずれかに記載のシート製造用押出装置。
〔19〕前記ノズルは、微細な孔を有するリング状の金属またはセラミックスで構成される上記〔17〕又は〔18〕に記載の押出装置。
〔20〕前記リング状の金属は、金属パウダーまたは金属繊維を焼結させた材料で構成される上記〔19〕に記載の押出装置。
〔21〕シート成形機のキャスティングロールおよび/またはキャスティングロール以降に、内部を減圧可能なチャンバーおよびシール機構を備えた真空チャンバー装置と、該真空チャンバー装置に付随する真空発生装置が配置されてなる発泡シート用製造装置。
〔22〕シート成形機のキャスティングロールおよび/またはキャスティングロール以降に、内部を減圧可能なチャンバーおよびシール機構を備えた真空チャンバー装置と、該真空チャンバー装置に付随する真空発生装置が配置されてなる上記〔1〕〜〔9〕のいずれかに記載のシート用製造装置。
〔23〕前記真空チャンバー装置は、減圧可能なチャンバーの内部を30KPa以下に減圧することが可能である上記〔21〕又は〔22〕に記載の製造装置。
The foam sheet of the present invention is applicable to reflectors, packaging materials, steel sheet laminating materials, separator materials, etc. due to its whiteness, weather resistance, heat retention, insulation, fine bubble content, etc. The scope of application is not limited to these. The foam sheet of the present invention can be particularly suitably used as a light reflecting plate for a planar light source used in a backlight mechanism of a liquid crystal display device.
The main and preferred embodiments of the present invention include the following.
[1] An unstretched foamed sheet comprising a thermoplastic resin, wherein 80% or more of the bubbles contained in the sheet have a cell diameter in the range of 0.1 to 20 μm and a porosity of 20 to A foam sheet that is 80%.
[2] The foamed sheet according to the above [1], wherein the tensile breaking elongation measured in an atmosphere at 100 ° C is 100% or more, and the tensile stress at 100 ° C and 100% elongation is 50 MPa or less.
[3] The foamed sheet according to the above [1] or [2], wherein the thermoplastic resin has a molten state fluidity (according to ASTM D1238-98) of 0.5 to 44 g / 10 min.
[4] The foamed sheet according to any one of [1] to [3], wherein the thermoplastic resin is an acrylic resin and / or a methacrylic resin.
[5] The foam sheet according to any one of the above [1] to [4], containing 0 to 3% by weight of a nucleating agent.
[6] The foam sheet according to any one of [1] to [5], wherein an embossed pattern is transferred on at least one side.
[7] A laminated sheet having two or more layers, wherein the foamed sheet according to any one of [1] to [6] is disposed at least one layer.
[8] The laminated sheet according to the above [7], wherein at least one non-foamed layer is disposed.
[9] The sheet according to any one of [1] to [8], wherein the reflectance in the visible light range is 85% or more and the total light transmittance is 10% or less.
[10] A light reflecting plate using the sheet according to any one of [1] to [9].
[11] A light reflector in which the sheet according to [10] is molded.
[12] A display device using the light reflecting plate according to [10] or [11].
[13] The method for producing a sheet according to any one of [1] to [9], including a step of foaming by extruding a thermoplastic resin in which a gas is dissolved.
[14] A step of forming a molten polymer of a thermoplastic resin in which a gas is dissolved in a non-foamed state,
Generating bubbles by exposing the sheet to a vacuum at a temperature of 50 to 200 ° C.,
A method for producing a foam sheet.
[15] A step of forming a molten polymer of a thermoplastic resin in which a gas is dissolved in a non-foamed state,
Generating bubbles by exposing the sheet to a vacuum at a temperature of 50 to 200 ° C.,
The manufacturing method of the sheet | seat in any one of said [1]-[9] containing.
[16] Any one of [1] to [9] and [13] to [15], wherein a thermoplastic resin in which a gas is dissolved and a thermoplastic resin in which a gas is not dissolved are coextruded. The manufacturing method of the sheet | seat of description.
[17] An extruder equipped with a screw, a cylinder, and a temperature control mechanism for the cylinder, wherein a gas supplied from a high-pressure gas supply unit provided outside the cylinder is introduced into an inner surface of a part of the cylinder. An extrusion apparatus for producing a foam sheet, comprising a nozzle for producing the foam sheet.
[18] An extruder equipped with a screw, a cylinder, and a temperature control mechanism for the cylinder, wherein a gas supplied from a high-pressure gas supply unit provided outside the cylinder is introduced into an inner surface of a part of the cylinder. The apparatus for producing a sheet according to any one of [1] to [9], further comprising a nozzle for the purpose.
[19] The extrusion apparatus according to [17] or [18], wherein the nozzle is made of a ring-shaped metal or ceramic having fine holes.
[20] The extrusion apparatus according to [19], wherein the ring-shaped metal is made of a material obtained by sintering metal powder or metal fiber.
[21] Foam formed by disposing a vacuum chamber device having a chamber capable of decompressing the inside and a sealing mechanism, and a vacuum generator attached to the vacuum chamber device, after the casting roll and / or the casting roll of the sheet forming machine Sheet manufacturing equipment.
[22] The above-mentioned structure in which a vacuum chamber apparatus provided with a chamber capable of decompressing the inside and a sealing mechanism, and a vacuum generation apparatus associated with the vacuum chamber apparatus are arranged after the casting roll and / or the casting roll of the sheet forming machine. [1] to [9] The sheet manufacturing apparatus according to any one of [9] to [9].
[23] The manufacturing apparatus according to [21] or [22], wherein the vacuum chamber device is capable of depressurizing the interior of the depressurizable chamber to 30 KPa or less.
1 押出装置1
1a 押出装置2
2 フィードブロック
3 ダイス
4 キャストロール
5 引き取りロール1
5a 引き取りロール2
6 真空チャンバー
7 真空ポンプ
8 シート
11 シリンダーブロック
11a ノズル部分のシリンダーブロック
12 スクリュー
13 ヒーター
14 ノズルブロック
14a ノズルメディア
14b 通気孔
15 ガス注入口
1
2
5a Take-
6 Vacuum chamber 7 Vacuum pump 8
Claims (12)
気体を溶解させたアクリル樹脂及び/又はメタクリル樹脂の溶融ポリマーを無発泡状態で押出およびシート化する工程、
シートを50〜200℃の温度条件下で真空に晒すことにより気泡を発生させる工程、
を含む工程により製造する、請求項1〜3のいずれかに記載の光反射板の製造方法。 The foam sheet,
A process of extruding and sheeting a molten polymer of acrylic resin and / or methacrylic resin in which gas is dissolved, in a non-foamed state;
Generating bubbles by exposing the sheet to a vacuum at a temperature of 50 to 200 ° C.,
The manufacturing method of the light reflecting plate in any one of Claims 1-3 manufactured by the process including this.
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
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JP2004224156A JP4093419B2 (en) | 2004-07-30 | 2004-07-30 | Foam sheet, manufacturing method and manufacturing apparatus thereof |
CN2005800258633A CN1993410B (en) | 2004-07-30 | 2005-07-27 | Foam board, method and apparatus for manufacturing the same |
KR1020077002313A KR100842524B1 (en) | 2004-07-30 | 2005-07-27 | Foamed sheet, and method and apparatus for producing same |
PCT/JP2005/013750 WO2006011521A1 (en) | 2004-07-30 | 2005-07-27 | Foamed sheet, and method and apparatus for producing same |
TW094125725A TWI347334B (en) | 2004-07-30 | 2005-07-29 | Foamed sheets, and methods and apparatuses for manufacturing the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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JP2004224156A JP4093419B2 (en) | 2004-07-30 | 2004-07-30 | Foam sheet, manufacturing method and manufacturing apparatus thereof |
Publications (3)
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JP2006045259A JP2006045259A (en) | 2006-02-16 |
JP2006045259A5 JP2006045259A5 (en) | 2007-03-15 |
JP4093419B2 true JP4093419B2 (en) | 2008-06-04 |
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JP2004224156A Expired - Fee Related JP4093419B2 (en) | 2004-07-30 | 2004-07-30 | Foam sheet, manufacturing method and manufacturing apparatus thereof |
Country Status (5)
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JP (1) | JP4093419B2 (en) |
KR (1) | KR100842524B1 (en) |
CN (1) | CN1993410B (en) |
TW (1) | TWI347334B (en) |
WO (1) | WO2006011521A1 (en) |
Families Citing this family (24)
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JP2007261071A (en) * | 2006-03-28 | 2007-10-11 | Sekisui Plastics Co Ltd | Light reflecting object and its manufacturing method |
KR100850793B1 (en) | 2006-05-09 | 2008-08-06 | 주식회사 엘지화학 | Foamed sheet for light reflection having good thermal conductivity and light reflectance |
JP4782617B2 (en) * | 2006-06-08 | 2011-09-28 | 帝人デュポンフィルム株式会社 | Polyester laminated film roll |
JP5211508B2 (en) * | 2007-02-28 | 2013-06-12 | 東レ株式会社 | White laminated polyester film for liquid crystal reflection |
JP4999073B2 (en) * | 2007-03-22 | 2012-08-15 | 古河電気工業株式会社 | Resin foam structure, light reflector, and method for producing resin foam structure |
JP5117757B2 (en) * | 2007-04-26 | 2013-01-16 | 日東電工株式会社 | Light reflecting member including polyolefin resin foam and method for producing the same |
JP2009086430A (en) * | 2007-10-01 | 2009-04-23 | Furukawa Electric Co Ltd:The | Light reflecting molded product |
KR101079004B1 (en) * | 2007-12-31 | 2011-11-01 | 주식회사 삼양사 | A collective fibers reinforced polymeric strip, method thereof, and a geogrid using the same |
JP5089436B2 (en) * | 2008-02-29 | 2012-12-05 | 古河電気工業株式会社 | Light reflecting sheet and manufacturing method thereof |
JP5259719B2 (en) * | 2008-08-04 | 2013-08-07 | 丸尾カルシウム株式会社 | Porous polyolefin resin foam sheet and method for producing the same |
US8779017B2 (en) | 2008-11-14 | 2014-07-15 | Mitsui Chemicals, Inc. | Foam and production method of the same |
JP5555525B2 (en) * | 2010-03-31 | 2014-07-23 | 積水化成品工業株式会社 | Method for producing resin foam sheet and reflection sheet |
CN102085689A (en) * | 2010-11-26 | 2011-06-08 | 卢文成 | Production method for inorganic foaming board |
JP2012189661A (en) * | 2011-03-09 | 2012-10-04 | Mitsubishi Plastics Inc | Olefin resin reflective material |
US11292163B2 (en) * | 2012-03-30 | 2022-04-05 | Mucell Extrusion, Llc | Method of forming polymeric foam and related foam articles |
CN104114365B (en) * | 2012-06-18 | 2016-01-20 | 古河电气工业株式会社 | Foamed sheet |
CN104165329B (en) * | 2014-08-13 | 2016-08-17 | 福建省锐驰电子科技有限公司 | One can plastic uptake reflector plate |
KR102353732B1 (en) * | 2015-02-16 | 2022-01-21 | 삼성디스플레이 주식회사 | Protection film and fabricating method of the same |
LU93110B1 (en) * | 2016-06-16 | 2018-01-09 | Tarkett Gdl Sa | Piezoelectret Film Production Method |
FR3080997B1 (en) * | 2018-05-14 | 2020-05-08 | Compagnie Generale Des Etablissements Michelin | EXTRUSION PLANT FOR COMPLEX PROFILES IN ELASTOMERIC MIXTURES |
CN112300436B (en) * | 2019-07-24 | 2022-12-13 | 中国科学院宁波材料技术与工程研究所 | Polymer foam material and preparation method thereof |
KR102119789B1 (en) * | 2020-02-03 | 2020-06-05 | 김하무 | manufacturing methods diffuser plate for display by cars |
KR102458420B1 (en) * | 2022-01-10 | 2022-10-25 | 안종호 | Silicone sheet forming device |
CN117801353B (en) * | 2023-10-20 | 2024-07-05 | 广东瑞捷新材料股份有限公司 | PEI foaming diffusion plate and preparation method thereof |
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KR940006459B1 (en) * | 1991-04-24 | 1994-07-20 | 주식회사 럭키 | Thermoplastic resin foaming composition |
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KR0139144B1 (en) * | 1994-03-30 | 1998-05-01 | 강박광 | Method of manufacturing blowing preform for midsole |
KR100363291B1 (en) * | 1994-12-27 | 2003-05-09 | 세키스이가세이힝코교가부시키가이샤 | Continuous manufacturing method and apparatus for thermoplastic polyester resin foam |
JP3115215B2 (en) * | 1995-10-05 | 2000-12-04 | 松下電器産業株式会社 | Low dielectric constant plastic insulating film and method of manufacturing the same |
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JP2001011228A (en) * | 1999-06-30 | 2001-01-16 | Toray Ind Inc | Foam and preparation thereof |
JP4036601B2 (en) * | 2000-06-05 | 2008-01-23 | 日東電工株式会社 | Polyolefin resin foam and method for producing the same |
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2004
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2005
- 2005-07-27 WO PCT/JP2005/013750 patent/WO2006011521A1/en active Application Filing
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JP2006045259A (en) | 2006-02-16 |
KR20070039106A (en) | 2007-04-11 |
CN1993410B (en) | 2012-05-30 |
WO2006011521A1 (en) | 2006-02-02 |
CN1993410A (en) | 2007-07-04 |
KR100842524B1 (en) | 2008-07-01 |
TW200615317A (en) | 2006-05-16 |
TWI347334B (en) | 2011-08-21 |
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