JPS61283541A - Manufacture of composite panel - Google Patents
Manufacture of composite panelInfo
- Publication number
- JPS61283541A JPS61283541A JP60124962A JP12496285A JPS61283541A JP S61283541 A JPS61283541 A JP S61283541A JP 60124962 A JP60124962 A JP 60124962A JP 12496285 A JP12496285 A JP 12496285A JP S61283541 A JPS61283541 A JP S61283541A
- Authority
- JP
- Japan
- Prior art keywords
- adhesive
- resin
- parts
- weight
- solvent
- 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.)
- Pending
Links
- 239000002131 composite material Substances 0.000 title claims description 16
- 238000004519 manufacturing process Methods 0.000 title claims description 10
- 239000000853 adhesive Substances 0.000 claims description 41
- 230000001070 adhesive effect Effects 0.000 claims description 41
- 239000000463 material Substances 0.000 claims description 31
- 239000002904 solvent Substances 0.000 claims description 18
- 238000000034 method Methods 0.000 claims description 16
- 229920005989 resin Polymers 0.000 claims description 16
- 239000011347 resin Substances 0.000 claims description 16
- 229920002803 thermoplastic polyurethane Polymers 0.000 claims description 11
- 239000005056 polyisocyanate Substances 0.000 claims description 9
- 229920001228 polyisocyanate Polymers 0.000 claims description 9
- 238000005507 spraying Methods 0.000 claims description 4
- 238000003825 pressing Methods 0.000 claims description 2
- 229920000877 Melamine resin Polymers 0.000 description 8
- 239000004640 Melamine resin Substances 0.000 description 8
- 229910000831 Steel Inorganic materials 0.000 description 8
- 239000010959 steel Substances 0.000 description 8
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
- 125000005442 diisocyanate group Chemical group 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000007921 spray Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 239000004593 Epoxy Substances 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000002788 crimping Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000005011 phenolic resin Substances 0.000 description 3
- 150000002989 phenols Chemical class 0.000 description 3
- 229920003002 synthetic resin Polymers 0.000 description 3
- 239000000057 synthetic resin Substances 0.000 description 3
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000004823 Reactive adhesive Substances 0.000 description 2
- 210000003323 beak Anatomy 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- -1 hydrogen compound Chemical class 0.000 description 2
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 150000003505 terpenes Chemical class 0.000 description 2
- 235000007586 terpenes Nutrition 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- 229920005992 thermoplastic resin Polymers 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 1
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical class [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- 229930194542 Keto Natural products 0.000 description 1
- QORUGOXNWQUALA-UHFFFAOYSA-N N=C=O.N=C=O.N=C=O.C1=CC=C(C(C2=CC=CC=C2)C2=CC=CC=C2)C=C1 Chemical compound N=C=O.N=C=O.N=C=O.C1=CC=C(C(C2=CC=CC=C2)C2=CC=CC=C2)C=C1 QORUGOXNWQUALA-UHFFFAOYSA-N 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004433 Thermoplastic polyurethane Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 230000001588 bifunctional effect Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 238000005056 compaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 125000000468 ketone group Chemical group 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000011120 plywood Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- AVWRKZWQTYIKIY-UHFFFAOYSA-N urea-1-carboxylic acid Chemical compound NC(=O)NC(O)=O AVWRKZWQTYIKIY-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明#′i表面材と裏面材とからなる複合/4ネルが
作業性良く得られる複合パネルの製造方法KIIAする
。DETAILED DESCRIPTION OF THE INVENTION (Industrial Application Field) The present invention #'i is a method for manufacturing a composite panel in which a composite/quad panel consisting of a front surface material and a back surface material can be obtained with good workability.
(従来の技v#)
例えば外観美麗な合成樹脂製の板等を表面材として、こ
れをfI4製の裏面板に接着して複合ノ嘴ネルを得る場
合、接着剤としては、従来よりクロロプレン系溶剤型接
着剤やエポキシ基又f)型接着剤等が用いられていた。(Conventional Technique v#) For example, when a synthetic resin plate with a beautiful appearance is used as a surface material and is bonded to a back plate made of fI4 to obtain a composite beak, the adhesive used is conventionally chloroprene-based. Solvent-based adhesives, epoxy-based adhesives, and type f) adhesives have been used.
しかしクロロプレン系溶剤型接着剤は、一般に、耐熱性
が不充分であり、又表面材と裏面材の双方に塗布するこ
と即ち両面塗布を必要とする為作業性が悪かった。特に
吹付は法によって接着剤を塗布する場合は、塗布面の裏
側にも接着剤が付着することが多く1.良好な外観を要
求される表面材の表面を汚損するという欠点があった。However, chloroprene-based solvent-based adhesives generally have insufficient heat resistance and have poor workability because they require coating on both the front and back surfaces, that is, double-sided coating. In particular, when applying adhesive by spraying, the adhesive often adheres to the back side of the applied surface.1. This has the disadvantage that it stains the surface of a surface material that requires a good appearance.
又、エポキシ系反応型接着剤の場合は、粘着性が極めて
小さい為、例えば表面材に反りがある場合#′i裏面材
に圧着した直後に浮きが生じ易いので圧締時間を長くし
なければならないという欠点があった。In addition, in the case of epoxy-based reactive adhesives, the adhesiveness is extremely low, so if the surface material is warped, for example, lifting may occur immediately after being crimped to the back surface material, so the crimping time must be extended. There was a drawback that it was not possible.
(発明が解決しようとする問題点)
本発明の目的は、上述の従来の/曵ネルの製法の欠点に
鑑みて、耐熱性が良好でかつ、片面塗布でも初期接着性
が良好々接着剤を用い、工業的に作業性良く複合パネル
を製造することができる複合ノ曵ネルの製造方法を提供
することKある。(Problems to be Solved by the Invention) In view of the above-mentioned drawbacks of the conventional / tunnel manufacturing method, the object of the present invention is to provide an adhesive that has good heat resistance and good initial adhesion even when coated on one side. It is an object of the present invention to provide a method for manufacturing a composite panel, which can be used to industrially manufacture a composite panel with good workability.
(問題点を解決する為の手段)
本発明方法は、粘着性付与樹脂を含有する熱可塑性ポリ
ウレタン樹脂−ボリイソシアネート系溶剤型接着剤を用
いるもので、該接着剤を裏面材に塗布し、溶剤を揮散さ
せた後、上記裏面材の接着剤塗布面Km面材を接触させ
て圧着し固化せしめることを特徴とする複合7鬼ネルの
製造方法である。(Means for Solving the Problems) The method of the present invention uses a thermoplastic polyurethane resin-polyisocyanate solvent-based adhesive containing a tackifying resin. After volatilizing the adhesive, the adhesive coated surface Km of the back surface material is brought into contact with the surface material and pressed and solidified.
本発明における熱可塑性ポリウレタン樹脂とけ、高分子
量線状ポリマーにして熱可塑性の性質を示すポリフレタ
ン樹脂を意味するが、完全熱可塑性樹脂は勿論、僅かに
部分!1!僑した不完全熱可塑性樹脂をも含むものであ
り、その分子量は特定されないが一般に重量平均分子量
がso、ooo〜20’0.000のものが用いられる
。Thermoplastic polyurethane resin in the present invention refers to a polyurethane resin that is a high molecular weight linear polymer and exhibits thermoplastic properties, but it is of course a completely thermoplastic resin, but only a small portion! 1! Although the molecular weight is not specified, those having a weight average molecular weight of so, ooo to 20'0.000 are generally used.
これは、分子量が低過ぎると接着剤自身の凝集力が小さ
く初期接着力が小さくなり逆圧分子量が高過ぎると溶剤
溶解性が悪くなり塗布作業性が低下する傾向があるから
である。This is because if the molecular weight is too low, the cohesive force of the adhesive itself will be low and the initial adhesive force will be low, and if the reverse pressure molecular weight is too high, the solvent solubility will be poor and the coating workability will tend to be reduced.
かかる熱可塑性樹脂は、例えば、両末端に水酸基を有す
るポリエステルもしくはポリエーテルの如き二官能性活
性水素化合物と、ジイソシアネート又はジイソシアネー
トとポリオールから得られる末端がNGO基のウレタン
ポリマーとを用い、全反応系中の活水水素基とイソシア
ネート基とを当量反応させて得ることが出来る。Such thermoplastic resins are produced by using, for example, a bifunctional active hydrogen compound such as a polyester or polyether having hydroxyl groups at both ends, and a urethane polymer having an NGO group at the end obtained from a diisocyanate or a diisocyanate and a polyol. It can be obtained by reacting the active water hydrogen groups and isocyanate groups in equivalent quantities.
又、硬化剤として用いられるポリイソシアネ−)Fi1
分子中VC2個以上のイソシアネート基を有する化合物
であり、その具体例としてけト 、ルエンジイソ
シアネート(TDI)、メチレンビスP 7 zニレン
ジイソシアネート(MDI)、ヘキサメチレンジイソシ
アネート、トリフェニルメタントリイソシアネート等が
挙げられる。In addition, polyisocyanate) Fi1 used as a curing agent
A compound having two or more VC isocyanate groups in the molecule, specific examples of which include keto, luene diisocyanate (TDI), methylene bisP 7 z nylene diisocyanate (MDI), hexamethylene diisocyanate, triphenylmethane triisocyanate, etc. .
これらの接着剤中の混合量は特定されるものではないが
、一般に、上記熱可塑性ポリフレタン樹脂100重量部
に対し5〜200重量部とされる。ポリイソシアネート
は、上記熱可塑性ポリフレタン樹脂と反応し、アロファ
ネート架橋を生じせしめて接着剤の耐熱性を高めるもの
と考えられる。Although the amount mixed in these adhesives is not specified, it is generally 5 to 200 parts by weight per 100 parts by weight of the thermoplastic polyurethane resin. It is believed that the polyisocyanate reacts with the thermoplastic polyurethane resin and causes allophanate crosslinking to increase the heat resistance of the adhesive.
本発明における粘着性付与樹脂の具体例としては、アル
キルフェノールとアルデヒドの反応物であるアルキルフ
ェノール樹脂、フェノール類とアルダヒトとの反応物で
あるフェノール類脂をテルペンで変性して得られたテル
ペン変性フェノール樹脂、ロジン変性フェノール樹脂、
ロジン、ロジンエステル、シクロヘキサノン樹脂、クマ
ロン樹脂、キシレンili% フェノール変性キシレン
樹脂、フタル酸樹脂等が挙けられ、特にアルキルフェノ
ール樹脂、テルペンフェノール樹脂、ロジン変性フェノ
ール樹脂、フェノール変性キシレン樹脂等が好ましく用
いられる。Specific examples of the tackifying resin in the present invention include alkylphenol resins that are a reaction product of alkylphenol and aldehyde, and terpene-modified phenol resins obtained by modifying phenolic fats that are a reaction product of phenols and aldahyde with terpenes. , rosin modified phenolic resin,
Examples include rosin, rosin ester, cyclohexanone resin, coumaron resin, xylene ili% phenol-modified xylene resin, phthalic acid resin, etc., and particularly preferred are alkylphenol resin, terpene phenol resin, rosin-modified phenol resin, phenol-modified xylene resin, etc. .
これら粘着性付与樹脂は通常、熱可重性ポリクレタン樹
脂100重量部に対し5〜200重量部用いられ、熱可
塑性ポリフレタン樹脂と相俟って接着剤に適度の初期粘
着性及び初期接着性を発現させ、複合/1ネル製造時の
片面塗り(裏面材にのみ接着剤を塗布すること)を可能
にするのである。These tackifying resins are usually used in an amount of 5 to 200 parts by weight per 100 parts by weight of thermoplastic polyurethane resin, and together with the thermoplastic polyurethane resin, they give the adhesive appropriate initial tackiness and initial adhesion. This enables single-sided coating (applying adhesive only to the back material) during composite/single-wall manufacturing.
接着剤の製造に用いられる溶剤としては、メチレンクロ
ライド、メチルエチルケトン、アセトン、酢酸エチル、
酢酸ブチル等のポリフレタンの良溶媒の他、これらと混
合して用いられるトルエン、キシレン、ヘキサン等のポ
リフレタンの貧溶媒が挙げられる。Solvents used in the manufacture of adhesives include methylene chloride, methyl ethyl ketone, acetone, ethyl acetate,
In addition to good solvents for polyurethane such as butyl acetate, there may be mentioned poor solvents for polyurethane such as toluene, xylene, hexane, etc., which are used in combination with these solvents.
接着剤を製造するVcFi、一般に、熱可塑性ポリウレ
タン樹脂及び粘着性付与樹脂を上記溶剤に溶解し、丈に
必要に応じて適宜の改質材を少量添加し、使用直前にポ
リイソシアネートを添加する。勿論予め溶剤に溶解して
おいたポリイソシアネートを添加しても差支えない。VcFi for producing adhesives generally involves dissolving a thermoplastic polyurethane resin and a tackifying resin in the above-mentioned solvent, adding a small amount of an appropriate modifier to the adhesive as needed, and adding a polyisocyanate immediately before use. Of course, polyisocyanate dissolved in a solvent in advance may be added.
本発明に用いられる表面材の具体例としては、合成樹脂
板、合成ゴム板、化粧板、合板、木材、鉄・アルミニウ
ム等の金属製板(塗装されていてもよい)、及びこれら
の積層体等が挙げられ、合成樹脂板や金属板等の非孔質
板が好ましく用いられる。又裏面材は、表面材と接着、
積層されて複合パネルとなされ、表面材と比較してより
人目に付きにくい(Mれる)状急で使用されるもので、
上記表面材と同様のものを用い得るが、主として金属板
や塗装金属板が用いられる。Specific examples of surface materials used in the present invention include synthetic resin boards, synthetic rubber boards, decorative boards, plywood, wood, metal boards such as iron and aluminum (which may be painted), and laminates thereof. Non-porous plates such as synthetic resin plates and metal plates are preferably used. In addition, the back material is bonded to the surface material,
It is laminated to form a composite panel and is used in a way that makes it less noticeable (M) than surface materials.
Although the same surface materials as those described above can be used, metal plates and painted metal plates are mainly used.
勿論、積層体であってもよい。Of course, a laminate may be used.
前記接着剤を裏面材に塗布するには、エアースプレー法
やエアーレススプレー法等の吹き付ケ法、カーテン70
−コーター法、ロールコータ−法及びナイフコーク−法
等の従来公知の方法を用い得る。吹き付は法は一般に、
塗布面の裏側に接着剤が著しく回り込むことが多いので
、表面材に接着剤を塗布する必要のない本発明において
好適に採用される。The adhesive can be applied to the backing material by a spraying method such as an air spray method or an airless spray method, or by a curtain 70 method.
- Conventionally known methods such as a coater method, a roll coater method, and a knife coke method can be used. The spraying method is generally
Since the adhesive often wraps around to the back side of the coated surface, it is preferably employed in the present invention, where there is no need to coat the adhesive on the surface material.
その後は常温でもしくは適宜加熱して溶剤を揮散させ、
上記裏面材の接着剤塗布面Kfc面材の隠れ面を接触さ
せてロールプレスや平面プレス等を用いて圧着する。圧
着は瞬間的であってもよく、作業性の点でロールプレス
を用いるのが有利である。このときの温度、圧力は表面
材や裏面材の種類、強度、要求寸法精度等により適宜選
択されるが、温度は一般に常温〜110℃程度とされ、
作業性の点で常温とするのが好ましい。After that, volatilize the solvent at room temperature or by heating as appropriate.
The adhesive coated surface of the backing material is brought into contact with the hidden surface of the Kfc facing material, and the adhesive is pressed using a roll press, a plane press, or the like. The crimping may be instantaneous, and it is advantageous to use a roll press in terms of workability. The temperature and pressure at this time are appropriately selected depending on the type of surface material and back material, strength, required dimensional accuracy, etc., but the temperature is generally about room temperature to 110 ° C.
From the viewpoint of workability, it is preferable to use room temperature.
(実施例) 以下単に部とあるのは重量部を表わす。(Example) Hereinafter, parts simply refer to parts by weight.
実施例1
メチルエチルブト2800部に、熱可塑性ポリエステル
ボリクレタン樹脂としてダスモクール400(住友パイ
エルクレタン社製、重量平均分子量約100,000)
を100部、粘着性付与樹脂としてタマノール581(
繁用化学社製、アルキルフェノール)を100部混合溶
解シ、得られた溶液にメチレンビスP7・=レンジイ
3ンシアネート(MDI)を50部添加して、ポッ
トライフが約24時間の溶剤型接着剤を得た。Example 1 Dasmocur 400 (manufactured by Sumitomo Peyer Cretan, weight average molecular weight approximately 100,000) as a thermoplastic polyester polycretan resin was added to 2800 parts of methyl ethyl but.
100 parts of Tamanol 581 (as a tackifying resin)
Mix and dissolve 100 parts of alkylphenol (manufactured by Shiyo Kagaku Co., Ltd.), and add methylene bis P7 = Renji to the resulting solution.
50 parts of triancyanate (MDI) were added to obtain a solvent-based adhesive with a pot life of about 24 hours.
この接着剤を、塗装鋼板(厚さ約α8%)の裏面にエア
ースプレー法によって約200μmの厚さに塗布し80
℃で3分間乾燥した。この裏面材の接着剤塗布面に、厚
さ約1%のメラミン樹脂化粧板を重ね合せ線圧2 If
/(至)、及び常温の条件で、ロールプレスを用いて両
者を圧着した。This adhesive was applied to the back side of a painted steel plate (thickness approximately α8%) to a thickness of approximately 200 μm using an air spray method.
It was dried for 3 minutes at ℃. A melamine resin decorative board with a thickness of approximately 1% is overlaid on the adhesive-coated surface of this backing material, and a linear pressure of 2 If is applied.
/ (To) and at room temperature, the two were pressed together using a roll press.
メラミン樹脂化粧板は、当初、周縁部に僅かの反りがあ
ったが、ロールプレスによる圧着後は鋼板に良く接着し
て反りは全くあめられなかった。その後宮i!にて約2
4時間放置して塗装鋼板と表面が美麗なメラミン樹脂化
粧板とが強固に接着した複合ノ曵ネルを得て、その引張
強度を測定した。結果#i第1表の通りであった。Initially, the melamine resin decorative board had a slight warp on the peripheral edge, but after being crimped with a roll press, it adhered well to the steel plate and the warp did not improve at all. Then Miya i! approx. 2
After being left for 4 hours, a composite panel in which the painted steel plate and the melamine resin decorative board with a beautiful surface were firmly adhered was obtained, and its tensile strength was measured. Results #i were as shown in Table 1.
比較例1
溶剤型接着剤をしてクロロプレン系接着剤(漬水化学工
業社製、ニスダイン2753 M 2−)を用いる以外
は、実施例1と同様にして塗装鋼板にのみ接着剤を塗布
してメラミン樹脂化粧板を重ね合せてロールで圧着した
。Comparative Example 1 Adhesive was applied only to the painted steel plate in the same manner as in Example 1, except that a chloroprene adhesive (Nisudine 2753 M 2-, manufactured by Tsukimizu Kagaku Kogyo Co., Ltd.) was used instead of a solvent-based adhesive. The melamine resin decorative boards were stacked one on top of the other and pressed together with a roll.
鋼板と化粧板との接着性が悪く、当初、化粧板の周縁に
生じていた反りは圧着後も是正されずに浮き上り、結局
、化粧板が鋼板から全面一1離して複合/曵ネル#′i
得られなかった。The adhesion between the steel plate and the decorative plate was poor, and the warpage that had initially appeared on the periphery of the decorative plate remained uncorrected even after crimping, and eventually the decorative plate was completely separated from the steel plate, resulting in a composite/rubber plate. 'i
I couldn't get it.
比較例2
実施例1で用いた塗装鋼板及びメラミン樹脂化粧板の双
方に、比較例1で用いたクロロプレン系溶剤型接着剤を
エアースプレー法により約200μmの厚さに塗布した
ところ、メラミン樹脂化粧板の表面に接着剤が裏回りし
て付着した。Comparative Example 2 When the chloroprene solvent-based adhesive used in Comparative Example 1 was applied to both the painted steel sheet and the melamine resin decorative board used in Example 1 to a thickness of approximately 200 μm using an air spray method, the melamine resin decorative board The adhesive stuck to the surface of the board.
その後80℃で3分間乾燥し、接着剤の塗布面同士を線
圧2 )f/mのロールプレスで圧着し、常温で24時
間放置後の引張強度を測定した。Thereafter, it was dried at 80° C. for 3 minutes, and the surfaces coated with the adhesive were pressed together using a roll press at a linear pressure of 2) f/m, and the tensile strength was measured after being left at room temperature for 24 hours.
結果Fi第1表の通ね耐熱性が不充分であった。As a result, the heat resistance shown in Table 1 was insufficient.
比較例3
エポキシ−ポリアミド基又E)fM接着剤(漬水化学工
業社製、ニスゲイン3100)を実施例1で用いたのと
同じ鋼板の裏面に約200μの厚さに塗布し、メラミン
樹脂化粧板を重ねて線圧2 K9/ tsの常温ロール
プレスで圧着した。このときメラミン樹脂化粧板の周縁
は反りにより僅かに浮き上っていた。そこで更に24時
間圧着(IQ/ctI、2o℃)した後、24時間放置
して複合パネルを得た。引張強度の測定結果F′i、第
1表の通りで、耐熱性は比較例2よりも改善されたが実
施例1よりも劣るものであった。Comparative Example 3 An epoxy-polyamide based adhesive (Nisgain 3100, manufactured by Uzukumizu Kagaku Kogyo Co., Ltd.) was applied to the back side of the same steel plate as used in Example 1 to a thickness of about 200 μm, and a melamine resin coating was applied. The plates were stacked and crimped using a room temperature roll press with a linear pressure of 2 K9/ts. At this time, the periphery of the melamine resin decorative board was slightly raised due to warping. Then, after pressing for another 24 hours (IQ/ctI, 2oC), the composite panel was left for 24 hours. The tensile strength measurement result F'i is as shown in Table 1, and the heat resistance was improved compared to Comparative Example 2, but inferior to Example 1.
@ 1 表
(発明の効果)
本発明方法によれば、上述のように、工業的に作業性良
く複合ノ畷ネルを製造することができる。@ 1 Table (Effects of the Invention) According to the method of the present invention, as described above, a composite channel can be produced industrially with good workability.
即ち本発明方法は、粘着性付与樹脂、熱可塑性ポリフレ
タン樹脂及びポリイソシアネートを含有する溶剤型接着
剤を用いて表面材及び裏面材から複合ノ嘴ネルを得るも
ので、表面材及び裏面材の双方に接着剤の塗布が必要な
従来のクロロプレン系溶剤型接着剤を用いる場合に比し
て、裏面材に接着剤を塗布する丈でよいので、塗布面積
が小さくて済む点、良好な外観が要求される表面材の表
面を汚損する虞れが無い点で、作業性良く複合パネルが
得られるのである。That is, the method of the present invention uses a solvent-based adhesive containing a tackifying resin, a thermoplastic polyurethane resin, and a polyisocyanate to obtain a composite beak from a face material and a backing material. Compared to using conventional chloroprene-based solvent-based adhesives, which require adhesive to be applied to the backing material, the adhesive only needs to be applied to the backing material, so the area to be applied is smaller, and a good appearance is required. Since there is no risk of staining the surface of the surface material being used, a composite panel can be obtained with good workability.
又、初期接着性が充分であるので、例えば表面材に僅か
な反りがあっても、エポキシ系反応型接着剤を用いる場
合の様に表面材及び裏面材を長時間圧締する必要がない
。In addition, since the initial adhesion is sufficient, even if the surface material is slightly warped, there is no need to press the surface material and the back material for a long time, unlike when using an epoxy-based reactive adhesive.
更に本発明によれば、ポリイソシアネートの作用により
耐熱性圧すぐれた複合ノ曵ネルが得られる。Furthermore, according to the present invention, a composite rope with excellent heat resistance and compaction can be obtained due to the action of the polyisocyanate.
Claims (1)
リイソシアネートを含有する溶剤型接着剤を裏面材に塗
布し、溶剤を揮散させた後、上記裏面材の接着剤塗布面
に表面材を接触させて圧着し固化せしめることを特徴と
する複合パネルの製造方法。 2、粘着性付与樹脂の含有量が熱可塑性ポリウレタン樹
脂100重量部に対し5〜200重量部であり、ポリイ
ソシアネートの含有量が熱可塑性ポリウレタン樹脂10
0重量部に対し5〜200重量部である第1項記載の製
造方法。 3、接着剤の塗布方法が吹き付け法である第1項もしく
は第2項記載の製造方法。[Scope of Claims] 1. After applying a solvent-based adhesive containing a tackifying resin, a thermoplastic polyurethane resin, and a polyisocyanate to the backing material and volatilizing the solvent, A method for manufacturing a composite panel, characterized by bringing surface materials into contact and pressing and solidifying them. 2. The content of the tackifier resin is 5 to 200 parts by weight per 100 parts by weight of the thermoplastic polyurethane resin, and the content of polyisocyanate is 10 parts by weight of the thermoplastic polyurethane resin.
The manufacturing method according to item 1, wherein the amount is 5 to 200 parts by weight relative to 0 parts by weight. 3. The manufacturing method according to item 1 or 2, wherein the adhesive application method is a spraying method.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60124962A JPS61283541A (en) | 1985-06-07 | 1985-06-07 | Manufacture of composite panel |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60124962A JPS61283541A (en) | 1985-06-07 | 1985-06-07 | Manufacture of composite panel |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS61283541A true JPS61283541A (en) | 1986-12-13 |
Family
ID=14898526
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60124962A Pending JPS61283541A (en) | 1985-06-07 | 1985-06-07 | Manufacture of composite panel |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61283541A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH05320614A (en) * | 1992-03-17 | 1993-12-03 | Sekisui Chem Co Ltd | Polyurethane adhesive and production of coating material of decorative sheet by using the same |
JPH06200229A (en) * | 1992-03-03 | 1994-07-19 | Sekisui Chem Co Ltd | Polyurethane adhesive and production of article covered with decorative sheet using the same |
US5846474A (en) * | 1992-12-21 | 1998-12-08 | Basf Corporation | Thermoplastic polyurethane with poly(hydroxyl group)-containing resin |
US5977268A (en) * | 1993-11-08 | 1999-11-02 | Basf Corporation | Thermoplastic polyurethane with poly(hydroxyl group)-containing resin |
US6306942B1 (en) | 2000-04-05 | 2001-10-23 | 3M Innovative Properties Company | Low temperature thermally activated water-dispersed adhesives |
US6310125B1 (en) | 2000-04-05 | 2001-10-30 | 3M Innovative Properties Company | Water-dispersed adhesive compositions |
US6444737B1 (en) | 2000-04-05 | 2002-09-03 | 3M Innovative Properties Company | Water-dispersed polymer stabilizer |
US6541550B1 (en) | 2000-04-05 | 2003-04-01 | 3M Innovative Properties Company | Low temperature thermally activated water-dispersed adhesive compositions |
-
1985
- 1985-06-07 JP JP60124962A patent/JPS61283541A/en active Pending
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH06200229A (en) * | 1992-03-03 | 1994-07-19 | Sekisui Chem Co Ltd | Polyurethane adhesive and production of article covered with decorative sheet using the same |
JPH05320614A (en) * | 1992-03-17 | 1993-12-03 | Sekisui Chem Co Ltd | Polyurethane adhesive and production of coating material of decorative sheet by using the same |
US5846474A (en) * | 1992-12-21 | 1998-12-08 | Basf Corporation | Thermoplastic polyurethane with poly(hydroxyl group)-containing resin |
US5977268A (en) * | 1993-11-08 | 1999-11-02 | Basf Corporation | Thermoplastic polyurethane with poly(hydroxyl group)-containing resin |
US6306942B1 (en) | 2000-04-05 | 2001-10-23 | 3M Innovative Properties Company | Low temperature thermally activated water-dispersed adhesives |
US6310125B1 (en) | 2000-04-05 | 2001-10-30 | 3M Innovative Properties Company | Water-dispersed adhesive compositions |
US6444737B1 (en) | 2000-04-05 | 2002-09-03 | 3M Innovative Properties Company | Water-dispersed polymer stabilizer |
US6541550B1 (en) | 2000-04-05 | 2003-04-01 | 3M Innovative Properties Company | Low temperature thermally activated water-dispersed adhesive compositions |
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