JPS60187533A - Preparation of resin laminated wooden board - Google Patents
Preparation of resin laminated wooden boardInfo
- Publication number
- JPS60187533A JPS60187533A JP59041228A JP4122884A JPS60187533A JP S60187533 A JPS60187533 A JP S60187533A JP 59041228 A JP59041228 A JP 59041228A JP 4122884 A JP4122884 A JP 4122884A JP S60187533 A JPS60187533 A JP S60187533A
- Authority
- JP
- Japan
- Prior art keywords
- film
- powder
- thermoplastic resin
- wooden board
- resin
- 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.)
- Granted
Links
- 229920005989 resin Polymers 0.000 title abstract description 23
- 239000011347 resin Substances 0.000 title abstract description 23
- 239000000843 powder Substances 0.000 claims abstract description 39
- 229920005992 thermoplastic resin Polymers 0.000 claims abstract description 30
- 239000002023 wood Substances 0.000 claims description 25
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 239000000463 material Substances 0.000 claims description 3
- 238000010309 melting process Methods 0.000 claims 1
- 238000000034 method Methods 0.000 abstract description 13
- 238000010438 heat treatment Methods 0.000 abstract description 11
- 238000002844 melting Methods 0.000 abstract description 9
- 230000008018 melting Effects 0.000 abstract description 9
- 229920000098 polyolefin Polymers 0.000 abstract description 5
- 230000006866 deterioration Effects 0.000 abstract description 2
- 230000004927 fusion Effects 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 11
- 239000011120 plywood Substances 0.000 description 10
- 239000005026 oriented polypropylene Substances 0.000 description 6
- 239000004743 Polypropylene Substances 0.000 description 5
- 229920001971 elastomer Polymers 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- -1 polypropylene Polymers 0.000 description 5
- 239000005060 rubber Substances 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 4
- 229920005672 polyolefin resin Polymers 0.000 description 4
- 229920001155 polypropylene Polymers 0.000 description 4
- 238000003475 lamination Methods 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 2
- 239000012792 core layer Substances 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 238000009503 electrostatic coating Methods 0.000 description 2
- 229920000554 ionomer Polymers 0.000 description 2
- 238000010030 laminating Methods 0.000 description 2
- 239000000088 plastic resin Substances 0.000 description 2
- 239000002356 single layer Substances 0.000 description 2
- 238000003892 spreading Methods 0.000 description 2
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-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
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 235000017166 Bambusa arundinacea Nutrition 0.000 description 1
- 235000017491 Bambusa tulda Nutrition 0.000 description 1
- 241001330002 Bambuseae Species 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 229920002943 EPDM rubber Polymers 0.000 description 1
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 235000015334 Phyllostachys viridis Nutrition 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000011425 bamboo Substances 0.000 description 1
- 229920006378 biaxially oriented polypropylene Polymers 0.000 description 1
- 239000011127 biaxially oriented polypropylene Substances 0.000 description 1
- 229920005549 butyl rubber Polymers 0.000 description 1
- 150000004653 carbonic acids Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000002788 crimping Methods 0.000 description 1
- ILUAAIDVFMVTAU-UHFFFAOYSA-N cyclohex-4-ene-1,2-dicarboxylic acid Chemical compound OC(=O)C1CC=CCC1C(O)=O ILUAAIDVFMVTAU-UHFFFAOYSA-N 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 229920006226 ethylene-acrylic acid Polymers 0.000 description 1
- 239000011094 fiberboard Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000009415 formwork Methods 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 229920000092 linear low density polyethylene Polymers 0.000 description 1
- 239000004707 linear low-density polyethylene Substances 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 229920001179 medium density polyethylene Polymers 0.000 description 1
- 239000004701 medium-density polyethylene Substances 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
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
- B29C63/00—Lining or sheathing, i.e. applying preformed layers or sheathings of plastics; Apparatus therefor
- B29C63/02—Lining or sheathing, i.e. applying preformed layers or sheathings of plastics; Apparatus therefor using sheet or web-like material
-
- 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
- B29C65/00—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor
- B29C65/02—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor by heating, with or without pressure
- B29C65/40—Applying molten plastics, e.g. hot melt
-
- 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
- B29C65/00—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor
- B29C65/48—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor using adhesives, i.e. using supplementary joining material; solvent bonding
- B29C65/486—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor using adhesives, i.e. using supplementary joining material; solvent bonding characterised by their physical form being non-liquid, e.g. in the form of granules or powders
-
- 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
- B29C65/00—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor
- B29C65/48—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor using adhesives, i.e. using supplementary joining material; solvent bonding
- B29C65/52—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor using adhesives, i.e. using supplementary joining material; solvent bonding characterised by the way of applying the adhesive
-
- 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
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/01—General aspects dealing with the joint area or with the area to be joined
- B29C66/05—Particular design of joint configurations
- B29C66/10—Particular design of joint configurations particular design of the joint cross-sections
- B29C66/11—Joint cross-sections comprising a single joint-segment, i.e. one of the parts to be joined comprising a single joint-segment in the joint cross-section
- B29C66/112—Single lapped joints
- B29C66/1122—Single lap to lap joints, i.e. overlap joints
-
- 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
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/40—General aspects of joining substantially flat articles, e.g. plates, sheets or web-like materials; Making flat seams in tubular or hollow articles; Joining single elements to substantially flat surfaces
- B29C66/41—Joining substantially flat articles ; Making flat seams in tubular or hollow articles
- B29C66/45—Joining of substantially the whole surface of the 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
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/70—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
- B29C66/71—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the composition of the plastics material of the parts to be joined
-
- 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
- B29K2711/00—Use of natural products or their composites, not provided for in groups B29K2601/00 - B29K2709/00, for preformed parts, e.g. for inserts
- B29K2711/14—Wood, e.g. woodboard or fibreboard
Landscapes
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Lining Or Joining Of Plastics Or The Like (AREA)
- Finished Plywoods (AREA)
- Laminated Bodies (AREA)
Abstract
Description
【発明の詳細な説明】
木兄ゆjは、木質板の表面に熱可塑性樹脂を積層するこ
とにより改良された木質板を製造する方法に関する。DETAILED DESCRIPTION OF THE INVENTION Yuj Kinoe relates to a method of manufacturing an improved wood board by laminating a thermoplastic resin on the surface of the wood board.
従来、挽き板、合板、集成木質板などの木質板表面を装
飾したり平滑化したりまたは表面硬度を向上するために
、木質板表面に樹脂フィルムを積層することが行われて
いる。一般に、木質板と樹脂フィルムを積層するにあた
っては、木質板の表面に樹脂フィルムを重ねて熱圧着す
る方法、または接着剤を用いて樹脂フィルムを木質板に
貼着する方法などが行われているが、これらの方法は樹
脂フィルムの木質板への接着性が十分ではない。この接
着性を改良するために、例えは木質板上に熱可塑性樹脂
の粉末を散布し、これを加熱浴融し、この上に熱可塑性
樹脂フィルムを供給して加熱出産することにより粉体浴
融樹脂を木質板の微細な凹凸に浸透させて接着性を向上
する方法が提系されている(%開昭58−128850
号公報)。Conventionally, a resin film has been laminated on the surface of a wooden board such as a sawn board, plywood, or laminated wood board in order to decorate or smooth the surface or to improve the surface hardness. Generally, when laminating a wood board and a resin film, methods are used such as stacking the resin film on the surface of the wood board and bonding it with heat, or using an adhesive to attach the resin film to the wood board. However, these methods do not provide sufficient adhesion of the resin film to the wood board. In order to improve this adhesion, for example, thermoplastic resin powder is sprinkled on a wooden board, this is melted in a heating bath, a thermoplastic resin film is supplied on top of this, and the thermoplastic resin is heated and then heated. A method has been proposed to improve adhesion by infiltrating the fine irregularities of a wooden board with a melted resin.
Publication No.).
しかしながら、この方法は積層フィルムの下に空隙が発
現したり、積層フィルムにヒンホールが発生し易く、ま
た積層合也に゛そりが発生し易いという問題があった。However, this method has problems in that voids are likely to appear under the laminated film, hingholes are likely to occur in the laminated film, and warpage is likely to occur during lamination.
本発明は、従来知られている樹脂積層木質板の製造方法
の、このような問題点を解消することを目的になされた
ものであって、本発明の樹脂積層木質板の製造方法は、
熱可塑性樹脂のフィルムまたはシート状物上に熱可塑性
樹脂の粉体を散布した後に、該粉体を加熱浴融し、次い
でこの粉体の溶融層を介して該フィルムまたはシート状
物を木質板上に圧着するものである。The present invention has been made to solve these problems of the conventionally known methods of manufacturing resin-laminated wood boards, and the method of manufacturing resin-laminated wood boards of the present invention includes
After scattering thermoplastic resin powder onto a thermoplastic resin film or sheet, the powder is melted in a heating bath, and then the film or sheet is transferred to a wooden board through the molten layer of the powder. It is crimped onto the top.
本光りJにおり−る熱可塑性樹J]dとしては、特に制
限はなく、ヤリえばポリオレフィン老樹b=、ポリオレ
フィン系樹脂に不飽和カルホンばもしくはその誘導体を
付加させた変性ポリオレフィン、ポリ塩化ビニル、ポリ
塩化ビニリチン、ポリスチレン、ABS樹脂、AS樹崩
、ポリアミド、ポリエステル、ポリウレタン、ボリカー
ホ不イト、アイオノマーなどフィルムまたはシート成形
可能なものがあげられる。上6U2ポリオレフィン系樹
脂としては、例えば高密度、中密度および低密度のポリ
エチレン、線状低密度ポリエチレン、ホリフロビレン、
ボリフデン、エナレンープロピレン共重合体、エチレン
−ブテン共重合体、プロピレン−ブテン共重合体、エチ
レン−酢酸ビニル共重合体、エチレン−アクリル酸エテ
ル共重合体、アイオノマーなどがあげられる。また、変
性ポリオレフィンとしては、上記ポリオレフィン系樹脂
および/またはオレフィン系のニジストマー、例えばポ
リインブチレンゴム、ブチルゴム、エチレンプロピレン
ゴム、エチレンープロピレンージエンターポリマー、エ
チレン−1−ブテンゴム、ブタンエンゴム、スチレン−
ブタジェンゴム、エチレン−フタジエンゴムなどを配合
したものに、不飽和カルホン酸もしくはその誘導体、例
えはマレイン酸、アクリル酸、メタクリル酸、エンド−
ビシクロ−[2,ン、1]−5−へブテン−2,6−ジ
カルボン酸、シス−4−シクロヘキセン−1,2−ジカ
ルボン酸もしくはこれらの酸無水物、エステル類、アミ
ド類、塩類などを反応させて、不飽和カルボン酸もしく
はその誘導体を0.001〜15M量多付加させたもの
などがあげられる。この変性ポリオレフィンの製造法は
、特に限定されず溶融法、溶液法など公知の方法を任意
に適用できる。There are no particular restrictions on the thermoplastic resin used in Honkori J, and examples include old polyolefin resin, modified polyolefin obtained by adding unsaturated calphonium or its derivatives to a polyolefin resin, and polyvinyl chloride. , polyvinyritine chloride, polystyrene, ABS resin, AS resin, polyamide, polyester, polyurethane, polycarbonate, ionomer, etc., which can be formed into a film or sheet. Examples of the above 6U2 polyolefin resin include high density, medium density and low density polyethylene, linear low density polyethylene, holiflopyrene,
Examples include borifdene, enalene-propylene copolymer, ethylene-butene copolymer, propylene-butene copolymer, ethylene-vinyl acetate copolymer, ethylene-acrylic acid ether copolymer, and ionomer. Examples of modified polyolefins include the above-mentioned polyolefin resins and/or olefin-based nidistomers, such as polyimbutylene rubber, butyl rubber, ethylene propylene rubber, ethylene-propylene-diene terpolymer, ethylene-1-butene rubber, butane-ene rubber, and styrene-butylene rubber.
Butadiene rubber, ethylene-phtadiene rubber, etc. are blended with unsaturated carbonic acids or derivatives thereof, such as maleic acid, acrylic acid, methacrylic acid, endo-
Bicyclo-[2,1,1]-5-hebutene-2,6-dicarboxylic acid, cis-4-cyclohexene-1,2-dicarboxylic acid, or their acid anhydrides, esters, amides, salts, etc. Examples include those in which an unsaturated carboxylic acid or a derivative thereof is added in an amount of 0.001 to 15M by reaction. The method for producing this modified polyolefin is not particularly limited, and any known method such as a melt method or a solution method can be applied.
上記の熱可塑性樹脂は、二植以上を混合して用いてもよ
い。また、必猥に応じて安定剤、着色剤、充填剤などを
任意に加えることができる。The above thermoplastic resins may be used in combination of two or more. Further, stabilizers, colorants, fillers, etc. can be added as desired.
本発明における熱可塑性樹脂のフィルムまたはシート状
物(以′)′フィルムという)は、上記の熱可塑性樹脂
を単層またはOl、層に成形したもので、無延伸のもの
、−軸延伸のものまたは二軸延伸のものなどが用いられ
るが、平滑性、強度、透明性、防湿性、硬度などの物性
に優れる二軸延伸フィルム、例えば二軸延伸ポリプロピ
レンフィルム(以下OPPフィルムといつ)カ木質板の
表]]II改良に好ましい。これらフィルムまたはシー
ト状物の厚さは、一般には10〜500μmのものが用
いられる。The thermoplastic resin film or sheet-like material (hereinafter referred to as ')' film) in the present invention is one in which the above-mentioned thermoplastic resin is molded into a single layer or a layer, and is unstretched or -axially stretched. Alternatively, biaxially oriented films such as biaxially oriented polypropylene films (hereinafter referred to as OPP films) with excellent physical properties such as smoothness, strength, transparency, moisture resistance, and hardness are used. [Table]] II preferred for improvement. The thickness of these films or sheet-like materials is generally 10 to 500 μm.
次に、本発明における熱可塑性樹脂の粉体は、前記の熱
可塑性樹脂からなる粉体で、特に接着性を向上させた変
性ポリオレフィンの粉体が好ましい。また、粉体の粒径
としては、50〜250μmの範囲のものが好ましい。Next, the thermoplastic resin powder in the present invention is a powder made of the above-mentioned thermoplastic resin, and particularly preferably a modified polyolefin powder with improved adhesiveness. Further, the particle size of the powder is preferably in the range of 50 to 250 μm.
粒径が250μm以上のものを用いると均一な厚みに粉
体を散布し難いと共に木質板との接着性が悪く、また粒
径が50μm以下のものは取扱いがやっかいで作業性が
劣るので好ましくない。If the particle size is 250 μm or more, it will be difficult to spread the powder to a uniform thickness and the adhesion to the wooden board will be poor, and if the particle size is less than 50 μm, it will be difficult to handle and workability will be poor, so it is not preferable. .
また、本発明における木質板としては、各種木材を木材
とする単板、合板、パーティクルボード、ファイバーボ
ードなどがあげられる。Furthermore, examples of the wooden board in the present invention include veneer made of various types of wood, plywood, particle board, fiberboard, and the like.
本発明は樹脂核層木質板を連続的に製造する場合に竹に
有用であり、以下連続的に行なう場合を図面を用いて説
明する。The present invention is useful for bamboo when a resin core layer wood board is manufactured continuously, and the case where the resin core layer is manufactured continuously will be explained below with reference to the drawings.
第1図は本発明の一実施例の工程を示す側面略図で、図
中1は熱可塑性樹脂フィルムで、ロール状に巻かれたも
のから連続して供給される。FIG. 1 is a schematic side view showing the steps of an embodiment of the present invention. In the figure, 1 is a thermoplastic resin film, which is continuously supplied from a rolled film.
2はフィルム予熱ヒーターで、供給される熱可塑性樹脂
フィルム1を加熱する。この場合の加熱温度は、該熱可
塑性樹脂の軟化点以上で融点未満の温度に加熱する。6
は熱可塑性樹脂の粉体、4は熱可塑性樹脂の粉体6を収
容するホッパーで、粉体6を加熱された熱可塑性樹脂旨
フィルム上に均一に落下散布する。この場合の散布の厚
さは、熱可塑性樹脂フィルム上で溶融し、木質板との接
着性が十分に得られるようにm〜節する。散布厚みが薄
いと加熱により浴融するが接着性が十分でなく、散布厚
みがP¥過ぎると加熱によるフィルム上での溶融が十分
ではなく好ましくない。散布量は熱5J塑性樹脂のフィ
ルムおよび粉体の種類によって適宜選択するが、一般に
は50〜2001tm程度の厚さが得られる範囲で行わ
れる。5は熱可塑性樹脂の粉体3のm融ヒーターで、フ
ィルム1上の粉末3を融点以上に加熱して浴融し、フィ
ルム1にに!r滲する。A film preheating heater 2 heats the supplied thermoplastic resin film 1. In this case, the heating temperature is higher than the softening point of the thermoplastic resin and lower than the melting point. 6
4 is a hopper containing thermoplastic resin powder, and 4 is a hopper containing thermoplastic resin powder 6, which drops and disperses the powder 6 uniformly onto the heated thermoplastic resin film. In this case, the thickness of the spray is determined to be from m to 100 m so that it melts on the thermoplastic resin film and has sufficient adhesion to the wooden board. If the thickness of the spray is too thin, it will melt in the bath when heated, but the adhesion will not be sufficient, and if the thickness of the spray is too thick, the melting on the film will not be sufficient due to heating, which is not preferable. The amount of spraying is appropriately selected depending on the type of thermo-5J plastic resin film and powder, but is generally carried out within a range that provides a thickness of about 50 to 2001 tm. 5 is a melting heater for the thermoplastic resin powder 3, which heats the powder 3 on the film 1 above its melting point and melts it in a bath to form the film 1! r ooze.
6はフィルム1の温度調IJ1〕ロールで、粉体浴融ヒ
ーター5で加熱されたフィルム10展面から温度調節を
行いフィルム1の面一変形を防止する。木質板7は、木
質板子熱ヒーター8で予熱され、ローラーコンベア9で
移送し、木質板70表面上に熱可塑性樹脂のフィルム1
を七の上の粉体浴融層l介して重ね、出潮ロール群10
で圧着して積層する。木質板7に積層するフィルム1は
、切断機11で切断して切り離し、樹脂積層木質板12
はローラーコンベア9で運ばれ木質板両側にはみだした
フィルムの耳を切断(図示していない)1−る。Reference numeral 6 denotes a temperature control IJ1 roll for the film 1, which controls the temperature from the rolled surface of the film 10 heated by the powder bath melting heater 5 to prevent flat deformation of the film 1. The wood board 7 is preheated by a wood board heater 8, transported by a roller conveyor 9, and a thermoplastic resin film 1 is placed on the surface of the wood board 70.
are layered through the powder bath melting layer 1 on top of 7, and the outflow roll group 10
Crimp and laminate. The film 1 to be laminated on the wood board 7 is cut and separated by a cutting machine 11, and the resin laminated wood board 12 is separated.
The film is transported by a roller conveyor 9 and the edges of the film protruding from both sides of the wooden board are cut off (not shown).
なお、上記の熱可塑性樹脂の粉体6の塗装は、第2図に
示すように粉体静電塗装機13に負の、接地されたフィ
ルム1の温#調節ロール乙に正の高圧靜′電気を印加し
、静電引力により粉体3をフィルム1の加熱向に散布す
ることもできる。The coating of the thermoplastic resin powder 6 is performed by applying a negative high pressure to the powder electrostatic coating machine 13 and a positive high pressure to the grounded temperature control roll B, as shown in FIG. It is also possible to apply electricity and scatter the powder 3 in the heating direction of the film 1 by electrostatic attraction.
この散布方法によれば粉末乙の飛散がなく散布厚さを積
度よく調整することができる。According to this spreading method, the powder B is not scattered and the thickness of the spreading can be precisely adjusted.
以上、本発明の方法によれば、木質板に積層した樹脂層
の下に空隙の発生や積層樹脂にピンホールが発生するこ
とがなく、また、木質板の加熱工程が短かく加熱温度も
低いために木質板のそりの発生や劣化を防止し、接層強
度に優れる樹脂積層木質板が得られる。また、樹脂層の
積層工程は、溶融粉体のプレスや樹脂積層加熱ローラー
が不要で簡素化および省エイ・ルギー型のもので、安価
に樹脂の櫃鳩工程乞連続して作業効率よく処理を行うこ
とのできるものである。As described above, according to the method of the present invention, there is no occurrence of voids under the resin layer laminated on the wooden board or pinholes in the laminated resin, and the heating process of the wooden board is short and the heating temperature is low. Therefore, a resin-laminated wood board can be obtained which prevents warping and deterioration of the wood board and has excellent bond strength. In addition, the resin layer lamination process does not require molten powder presses or resin lamination heating rollers, making it simple, energy-saving, and energy-saving. It is something that can be done.
本発明の方法により得られる樹脂積層木質板は、化粧合
板、コンクリート型枠板など各種用途に使用できる。The resin laminated wood board obtained by the method of the present invention can be used for various purposes such as decorative plywood and concrete form board.
次に、本発明を実施例により詳細に睨明する。Next, the present invention will be explained in detail with reference to examples.
実施例1
図1に示される連続樹脂積層木質板製造装置を用いて、
厚さ50μmの二11!llI延伸ポリプロピレンフィ
ルム(以下OPPフィルムとい5)1をフィルム予熱ヒ
ーター2で温度140℃に加熱し、OPPフィルムの加
熱向に粒径100〜200μηLの変性ポリプロピレン
(ポリプロピレンに無水マレモノ廠を付刃0させたもの
)の粉体3をホンパー4から厚さか約40μyetにな
るように落下数−布した。この1侍のOPPフィルムの
送り速度は6 m /分であった。次に、粉体浴融ヒー
ター5で温度180℃に加熱し、変性ポリエチレンの粉
体をOPPフィルムに浴着した。Example 1 Using the continuous resin laminated wood board manufacturing apparatus shown in FIG.
211 with a thickness of 50 μm! A stretched polypropylene film (hereinafter referred to as OPP film 5) 1 is heated to a temperature of 140°C with a film preheating heater 2, and a modified polypropylene (polypropylene is coated with anhydrous male monolayer) having a particle size of 100 to 200 μηL is heated in the heating direction of the OPP film. Powder 3 of the above was dropped from the ompper 4 to a thickness of approximately 40 μyet. The feeding speed of this 1 Samurai OPP film was 6 m/min. Next, the powder bath was heated to a temperature of 180° C. using a powder bath melting heater 5, and the modified polyethylene powder was bath-deposited on the OPP film.
この時、フィルムの温度調節ロール6は温度を140℃
に保持した。At this time, the temperature control roll 6 of the film adjusts the temperature to 140°C.
was held at
厚さ12關の合板70表面を木質板子熱ヒーター8で9
5℃に加熱した上に、該OP I)フィルムの粉体溶着
面を接合し、圧着ロール群で圧着し、フィルムの切断を
行って!*層樹脂の厚さ90μ慾のoppフィルム積層
合板を得た。得られたoppフィルム値層金層合板層樹
脂層には望隙およびピンホールは認めもオレず、また相
ノー合板のそりも発生しなかった。槓贋樹jJホの18
0°剥離強度(剥離速度7α/分、以下同じ)は5m
/ 5.5 clnであった。The surface of the plywood 70 with a thickness of 12 mm is heated 9 times with a wood board heater 8.
After heating to 5°C, the powder-welded surfaces of the OP I) film were joined together, crimped with a group of pressure rolls, and the film was cut! *Opp film laminated plywood with a resin layer thickness of 90 μm was obtained. No voids or pinholes were observed in the resulting OPP film layer, gold layer, plywood layer, or resin layer, and no warping of the plywood occurred. 18 of JJ Ho
0° peel strength (peel speed 7α/min, same below) is 5 m
/5.5 cln.
また、○PPフィルム積層合板をコンクリート型枠板と
して用いたところ、コンタリートとの剥離性がよ(、フ
ィルムの剥離およびコンクリートの付着がみもれず、従
来品に比べて繰返し使用回数がはるかに向上1−るもの
であった。In addition, when PP film laminated plywood was used as a concrete formwork board, it showed good peelability from contourite (no peeling of the film or adhesion of concrete, and the number of repeated uses was much improved compared to conventional products. It was one thing.
災施例2
実施例1に2いて、変性ポリプロピレンの粉体3の散布
を、第2図に示すような静電塗装機16を用いて行った
以外は同様にしてQPPフィルム積j積層板を得た。得
られたO、Pトフイルム積層合板は、空隙およびピンホ
ールは認められず、また槓ノー合板のそりも発生しなか
った。Accidental Example 2 A QPP film laminate was prepared in the same manner as in Example 1, except that the modified polypropylene powder 3 was sprayed using an electrostatic coating machine 16 as shown in FIG. Obtained. In the obtained O, P film laminated plywood, no voids or pinholes were observed, and no warping of the plywood occurred.
積層樹脂の180°剥離強度は51<g/ 3.5.7
F+であった。The 180° peel strength of the laminated resin is 51<g/3.5.7
It was F+.
第1図は、本究明の一実施態様を示す側面概略図で、第
2図は他の実施態様であるn電塗装工程の状態乞示す概
略図である。
1・・熱町塑性樹IIdフィルム、2・フィルム予熱ヒ
ーター、ろ・熱oJ塑性樹脂粉体、4・−ホッパー、5
・・粉体浴融ヒーター、6・ フィルム温度1=j m
I’−ラー、7・・木質板、8 木質板子熱ヒーター
、9 ・ローラーコンベア、10−・・圧着ロール、1
1・切断機、12・・・樹脂抗層木質板13・・・粉体
静’ttJ、m装機
代理人 内 1) 明
代理人 萩 原 亮 −
第2図FIG. 1 is a schematic side view showing one embodiment of the present invention, and FIG. 2 is a schematic diagram showing the state of the n-electronic coating process, which is another embodiment. 1. Atsumachi plastic tree IId film, 2. Film preheating heater, filter, thermo oJ plastic resin powder, 4.-Hopper, 5
・・Powder bath melting heater, 6・Film temperature 1=j m
I'-Lar, 7...Wood board, 8 Wood board heat heater, 9 - Roller conveyor, 10-...Crimping roll, 1
1. Cutting machine, 12... Resin anti-layer wood board 13... Powder static 'ttJ, m equipment representative 1) Akira representative Ryo Hagihara - Figure 2
Claims (1)
樹脂の粉体を散布した後に、該粉体な加熱溶融し、次い
でこの粉体の溶融ノーを介して該フィルムまたはシート
状物を木質板上に圧着することを%徴とする樹脂積層木
質板の製造方法。After scattering thermoplastic resin powder onto a thermoplastic resin film or sheet, the powder is heated and melted, and then the film or sheet is placed on a wooden board through the melting process. A method for producing resin-laminated wood boards that is characterized by being crimped to a material.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59041228A JPS60187533A (en) | 1984-03-06 | 1984-03-06 | Preparation of resin laminated wooden board |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59041228A JPS60187533A (en) | 1984-03-06 | 1984-03-06 | Preparation of resin laminated wooden board |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60187533A true JPS60187533A (en) | 1985-09-25 |
| JPH0378252B2 JPH0378252B2 (en) | 1991-12-13 |
Family
ID=12602551
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59041228A Granted JPS60187533A (en) | 1984-03-06 | 1984-03-06 | Preparation of resin laminated wooden board |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60187533A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1010505A1 (en) * | 1998-12-17 | 2000-06-21 | Bush Industries, Inc. | Veneer and method of manufacture |
-
1984
- 1984-03-06 JP JP59041228A patent/JPS60187533A/en active Granted
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1010505A1 (en) * | 1998-12-17 | 2000-06-21 | Bush Industries, Inc. | Veneer and method of manufacture |
| US6686037B2 (en) | 1998-12-17 | 2004-02-03 | Bush Industries, Inc. | Wood veneer comprising ethylene styrene interpolymer layer and process for producing the same |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0378252B2 (en) | 1991-12-13 |
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