JPH0137266B2 - - Google Patents

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Publication number
JPH0137266B2
JPH0137266B2 JP16581581A JP16581581A JPH0137266B2 JP H0137266 B2 JPH0137266 B2 JP H0137266B2 JP 16581581 A JP16581581 A JP 16581581A JP 16581581 A JP16581581 A JP 16581581A JP H0137266 B2 JPH0137266 B2 JP H0137266B2
Authority
JP
Japan
Prior art keywords
decorative
sheet
polyvinyl chloride
surface protection
adhered
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
Application number
JP16581581A
Other languages
Japanese (ja)
Other versions
JPS5867444A (en
Inventor
Kazuo Noya
Shigeru Kumagai
Noritaka Fujioka
Akihiro Yamamoto
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
SUN A CHEMICAL IND
Original Assignee
SUN A CHEMICAL IND
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by SUN A CHEMICAL IND filed Critical SUN A CHEMICAL IND
Priority to JP16581581A priority Critical patent/JPS5867444A/en
Publication of JPS5867444A publication Critical patent/JPS5867444A/en
Publication of JPH0137266B2 publication Critical patent/JPH0137266B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は鋼板又は木質合板の表面に化粧用ポリ
塩化ビニルシートが接着されてなる化粧板及びそ
の製造法に関するものである。 鋼板又は木質合板の片面又は両面を、着色され
又は模様を印刷されたポリ塩化ビニルシートを接
着することにより化粧した板(以下これを塩ビ化
粧板という)は家具や電気機器の製造に、あるい
は建材として、広く利用されているが、化粧板の
化粧面には、化粧板の製造後使用開始までの種々
の段階における損傷や汚染を防ぐために、表面保
護フイルムを接着しておくことが多い。表面保護
フイルムは、化粧板の通常の取扱いや加工によつ
ては剥離しない程度に、但し化粧板又はそれを用
いた建物等の構造物の使用開始時には容易に剥離
することができる程度に、適度の接着力をもつて
化粧板に接着されていなければならないことはも
ちろんであるが、更にその接着が長期にわたり安
定であることも重要であつて、経時変化により保
護フイルムがひとりでにはがれたり、はがしたあ
とに“糊残り”するようなことがあつてはならな
い。ところが従来の表面保護フイルムは、ポリ塩
化ビニルシート(以下塩ビシートという)表面の
保護に用いるには問題があるものであつた。すな
わち、表面保護フイルムとしては、基材フイルム
に感圧接着剤を塗布した感圧型のもの、及び基材
フイルムに低融点熱可塑性樹脂を積層した感熱型
のものの2種類があるが、いずれの型のものも、
化粧板の塩ビシートに貼り合わされた後の接着が
不安定であるという欠点を持つ。例えば感圧型保
護フイルムとしてはアクリル系又はゴム系の感圧
接着剤を用いたものが代表的であるが、これらの
接着剤はポリ塩化ビニル中の可塑剤の影響を受け
易く、接着後1〜2週間もすると、接着力が低下
するばかりでなく保護フイルムをはがしたときに
接着剤が塩ビシート側に残り、表面が汚くなくな
る。また接着剤としてエチレン・酢酸ビニル共重
合樹脂(又はこれとポリイソブチレンとの混合
物)、エチレン・アクリル酸エチル共重合樹脂な
どを用いた感熱型保護フイルムの場合も、接着力
の経時劣化が著しい。 上述のような塩ビシート面の保護における特有
の課題を解決する手段として、特公昭52−6309号
公報には溶解度パラメーターが8.0〜11.0の含塩
素重合物を混合したエチレン系重合物を接着剤と
して用いる方法が開示されている。しかしなが
ら、この方法は接着力の安定化にはあるていど有
効であるものの、表面保護フイルムの製造工程に
おいて含塩素重合物が熱分解して腐食性のガスを
発生して装置腐食及び環境汚染の原因となるばか
りか、化粧板からはがした保護フイルムを焼却処
分する際にも有毒かつ腐食性のガスを発生させる
ものであるから、決して好ましい方法ではない。 本発明は上述のような従来の塩ビ化粧板の表面
保護手段の欠点を解消したもので、ポリ塩化ビニ
ル用可塑剤を混入したエチレン・酢酸ビニル共重
合樹脂によりポリオレフイン系表面保護フイルム
が接着されていることを特徴とする塩ビ化粧板及
びそれを有利に製造する方法を提供するものであ
る。 本発明における表面保護フイルムの接着剤に用
いるエチレン・酢酸ビニル共重合樹脂としては、
酢酸ビニル含有量20〜50重量%のものが好まし
い。この値が20重量%を下回るものは接着力が小
さすぎるだけでなく、必要量のポリ塩化ビニル用
可塑剤を均一に混入することができない。一方50
重量%をこえるものは、溶融押出成形により表面
保護フイルムの基材フイルムに積層する作業が困
難である。またこの樹脂のメルトインデツクス
は、後記可塑剤を混入した状態で2〜50程度であ
ることが望ましい。 エチレン・酢酸ビニル樹脂に混入するポリ塩化
ビニル用可塑剤としては、ジオクチルフタレート
のようなフタル酸誘導体、ジオクチルアジペート
のようなアジピン酸誘導体、ジオクチルアゼレー
トのようなアゼライン酸誘導体、ジオクチルセバ
ケートのようなセバシン酸誘導体、ジオクチルマ
レエートのようなマレイン酸誘導体、その他フマ
ル酸、トリメリツト酸、クエン酸、イタコン酸、
オレイン酸、リシノール酸、ステアリン酸、各種
スルホン酸、リン酸、グリコール酸等の誘導体な
ど、ポリ塩化ビニルの可塑剤として使用できる化
合物のうち、常温で液体のものを使用する。常温
で固体のイタコン酸モノメチル、ジステアリン酸
ジエチレングリコールなどは、理由は定かでない
が、使用しても効果がない。 可塑剤は化粧用塩ビシートに最も多く含まれて
いる可塑剤(いわゆる第一次可塑剤)と同一であ
るとき混入効果が最大であるが、同一でなければ
ならないというわけではない。エチレン・酢酸ビ
ニル共重合樹脂に対する可塑剤の混入率は2〜30
重量%、好ましくは5〜15重量%とする。 表面保護フイルムの基材となるポリオレフイン
フイルムとしては、特にメルトインデクスが2〜
50(好ましくは6〜15)の低密度ポリエチレン及
び中密度ポリエチレンからなるフイルムが物性面
から好ましい。 表面保護フイルムと化粧板の間の接着力は、一
般に50〜200g/25mm程度(大きくても500g/25
mm迄)が適当とされており、本発明の化粧板にお
いても上記範囲内の接着力のものとなるよう、接
着剤の特性に応じて接着条件を変更するが、自然
剥離の恐れがない限り、20g/25mm程度まで接着
力を下げても差支えない。 本発明の化粧板において、化粧用の塩ビシート
及びそれが接着されている鋼板、木質合板等は、
なんら限定されるものではない。 上述のような本発明の化粧板は、表面保護フイ
ルムの基材としてポリオレフインフイルムを用
い、かつ接着剤としてポリ塩化ビニル用可塑剤を
混入したエチレン・酢酸ビニル共重合樹脂を用い
たことにより、可塑剤の作用機構は未だ確認され
ていないが、保護フイルムの接着が長時間安定で
あり、したがつて苛酷な条件下に置いても保護フ
イルムが自然にはがれたり、保護フイルムをはが
した後に保護フイルムの接着剤が残つて化粧板表
面を汚したりすることはない。更に化粧板からは
がした後の保護フイルムは、接着剤層が非粘着性
であり、また焼却しても腐食性・刺激性のガスを
発生しないから、廃棄処分が楽であるという利点
もある。 本発明の化粧板は、常法どおり、塩ビ化粧板を
製造したのち表面保護フイルムを接着する方法に
より製造してもよいが、特に有利な製法は、以下
に詳述するような本発明による製法である。 本発明の製法では、第1図に示したように、鋼
板、木質合板等の基板に接着する化粧用塩ビシー
ト1にあらかじめ表面保護フイルム2を接着した
積層シートを用意する。但し図中3は保護フイル
ム用の、前記組成の接着剤層であり、1aは化粧
板の表面となる面、1bは基板に接着される面で
ある。この積層シートはどのような製法によつて
製造されたものであつても差支えないが、積層シ
ート内に残る歪が少ないため接着力が小さくても
自然剥離を起こしにくい点で特に好ましいのが次
のような方法で製造されたものである。すなわ
ち、表面保護フイルムの基材となるポリオレフイ
ン樹脂と接着剤構成成分とを別々の押出機中で加
熱溶融後、溶融物を層状に合流させてTダイから
押出すいわゆる共押出法により製膜し、得られた
ポリオレフイン及び接着剤からなる積層物を、そ
れがまだ溶融状態にある間に、化粧用塩ビシート
に第1図のような配置で圧着するのである。 本発明の製造法では第1図のような積層シート
を、面1bを接着面として鋼材、木質合板等の基
板に接着するが、この接着は、常法により化粧用
塩ビシートを基板に接着する場合と同様にして行
えばよい。 第2図はこのようにして作られた本発明の化粧
板を示し、4は基板、5は第1図の積層シートと
基板4との接着に用いられた接着剤である。 上述のような本発明の製造法の利点は次のとお
りである。 化粧用塩ビシートが基板に接着される段階で
すでに保護フイルムにより保護されているか
ら、接着工程における表面損傷が避けられる。 感熱型表面保護フイルムを従来の常法に従つ
て塩ビ化粧板に接着するには熱容量の大きい化
粧板全体を接着可能温度まで加熱しなければな
らず、消費熱量が大きいだけでなく均一加熱が
むずかしいため、接着強度に斑を生じ易いとい
う問題があつた。塩ビ鋼板の場合、鋼板に塩ビ
シートを加熱状態で接着した後、直ちに表面保
護フイルムを接着することによつて消費熱量を
節減する方法もあるが、この場合も温度斑に基
づく接着斑を生じるのは避けられず、また保護
フイルムの接着工程が塩ビ鋼板製造ラインに組
込まれることにより接着条件が制約を受けるか
ら、加熱温度や圧着時間を変更すれば接着力を
調節できるという感熱型の利点を生かせない。
これに対して本発明の方法では、接着力のデリ
ケートな調節を必要とする保護フイルムの接着
は基板に接着する前の薄い塩ビシートとの間で
済ませておくから、上記従来法の欠点はすべて
解消される。 基板に接着する前の化粧用塩ビシートに感熱
型表面保護シートを接着し積層シートとしてお
く試みが従来無かつたわけではないが、この方
法は、積層直後から塩ビシート中の可塑剤の移
行による接着力低下が始まるため、積層シート
の状態での保存期間の長短によつて製品におけ
る保護フイルムの接着力が変動してしまうとい
う欠点があり実際的でなかつたのに対し、本発
明の方法では可塑剤による接着力低下がきわめ
て少ない独特の接着剤を用いたことによりこの
問題が解決されている。 以下実施例を示して本発明を説明する。なお第
1表に示した接着力は、幅25mmの試料について、
引張速度300mm/分、剥離角180゜、23℃・65%RH
の条件で、東洋ボールドウイン製テンシロンによ
り測定したものである。 実施例 1 基材:密度0.920、MI10のポリエチレン。 接着剤:酢酸ビニル含有量28重量%、MI5のエチ
レン・酢酸ビニル共重合樹脂にジオクチルフタ
レートを10重量%混入したもの。 表面保護フイルム用の上記素材を共押出法によ
り前者が厚さ50μ、後者が厚さ20μの積層物とし
て押出し、それがまだ溶融状態にある間に、塩ビ
鋼板製造用の塩ビシート(可塑剤としてジオクチ
ルフタレートを含有する)に、接着剤層を内側に
して圧着する。その際、押出温度や圧着条件を
種々変更することにより8種類の積層シート(a
〜h)を製造した。 各積層シートを30日間常温で保存後、鋼板に接
着して塩ビ鋼板を製造したが、接着中はもちろ
ん、得られた塩ビ鋼板に曲げ、切断等の後加工を
施しても、保護フイルムの自然剥離は起こらなか
つた。 実施例 2 基材:密度0.924、MI10のポリエチレン。 接着剤:酢酸ビニル含有量20重量%、MI5のエチ
レン・酢酸ビニル共重合体にジオクチルアジペ
ートを5重量%混入したもの。 表面保護フイルム用の上記素材を、実施例1の
場合と同様にして、前者が厚さ30μ、後者が厚さ
40μの積層物とし、更にジオクチルフタレートを
含有する塩ビシートに圧着する。その際圧着条件
を変えることにより、2種類の積層シート(i、
j)を製造した。 各積層シートを30日間常温で保存後、合板に接
着して塩ビ化粧合板を製造した。接着中及び得ら
れた化粧合板の切断加工中、表面保護フイルムの
自然剥離は起こらなかつた。 実施例 3 基材:密度0.918、MI10のポリエチレン。 接着剤:酢酸ビニル含有量45重量%、MI2のエチ
レン・酢酸ビニル共重合樹脂にジオクチルフタ
レート20重量%を混入したもの。 表面保護フイルム用の上記素材を、実施例1の
場合と同様にして、前者が厚さ40μ、後者が厚さ
30μの積層物とし、更にジオクチルフタレートを
含有する塩ビシートに圧着する。その際圧着条件
を変えることにより、2種類の積層シート(k、
l)を製造した。得られた積層シートを次いで鋼
板に接着して塩ビ鋼板を製造した。 〔接着力の比較試験〕 上記各実施例による製品について、保護フイル
ムと化粧用塩ビシートの間の接着力及びその経時
変化を調べた結果を第1表に示す。但し試験は便
宜上基板に接着してない積層シートについて行
い、10g/cm2の荷重を加えて40℃又は65℃に加熱
することにより経時変化を促進した。なお表中に
示した比較例1及び2は各実施例と同様の製法に
よる次のような構成のものである。 保護フイルム基材:実施例1と同じ。 接着剤:酢酸ビニル含有量28重量%、MI5のエチ
レン・酢酸ビニル共重合樹脂。層厚20μ。 塩ビシート:実施例1と同じ。
The present invention relates to a decorative board in which a decorative polyvinyl chloride sheet is adhered to the surface of a steel plate or wood plywood, and a method for manufacturing the same. Boards made by adhering colored or patterned polyvinyl chloride sheets to one or both sides of steel plates or wood plywood (hereinafter referred to as vinyl chloride decorative boards) are used in the manufacture of furniture and electrical equipment, or as building materials. However, a surface protection film is often adhered to the decorative surface of a decorative board in order to prevent damage and contamination at various stages from the manufacture of the decorative board to the start of use. The surface protection film should be applied in a moderate amount to the extent that it will not peel off during normal handling or processing of the decorative board, but to the extent that it can be easily peeled off when the decorative board or a structure using it, such as a building, is started to be used. It goes without saying that it must be bonded to the decorative board with an adhesive strength of There should be no ``glue residue'' left after applying the adhesive. However, conventional surface protection films have problems when used to protect the surface of polyvinyl chloride sheets (hereinafter referred to as vinyl chloride sheets). In other words, there are two types of surface protection films: a pressure-sensitive type in which a pressure-sensitive adhesive is applied to a base film, and a heat-sensitive type in which a low-melting thermoplastic resin is laminated on a base film. The ones of
It has the disadvantage that the adhesion is unstable after being bonded to the decorative PVC sheet. For example, pressure-sensitive protective films typically use acrylic or rubber-based pressure-sensitive adhesives, but these adhesives are easily affected by the plasticizer in polyvinyl chloride, and after bonding, After two weeks, not only does the adhesive force deteriorate, but when the protective film is removed, the adhesive remains on the PVC sheet side, leaving the surface dirty. Furthermore, in the case of heat-sensitive protective films that use ethylene/vinyl acetate copolymer resin (or a mixture of this and polyisobutylene), ethylene/ethyl acrylate copolymer resin, or the like as an adhesive, the adhesive strength deteriorates significantly over time. As a means to solve the above-mentioned unique problems in protecting the surface of PVC sheets, Japanese Patent Publication No. 1983-6309 discloses that an ethylene polymer mixed with a chlorine-containing polymer with a solubility parameter of 8.0 to 11.0 is used as an adhesive. A method for use is disclosed. However, although this method is somewhat effective in stabilizing adhesive strength, the chlorine-containing polymer thermally decomposes during the manufacturing process of the surface protection film and generates corrosive gas, resulting in equipment corrosion and environmental pollution. This is not a preferable method because it not only causes a problem but also generates toxic and corrosive gas when the protective film removed from the decorative board is incinerated. The present invention solves the above-mentioned drawbacks of conventional surface protection means for PVC decorative boards, and a polyolefin surface protection film is bonded with an ethylene/vinyl acetate copolymer resin mixed with a plasticizer for polyvinyl chloride. The present invention provides a PVC decorative board and a method for advantageously manufacturing the same. The ethylene/vinyl acetate copolymer resin used as the adhesive for the surface protection film in the present invention includes:
Preferably, the vinyl acetate content is 20 to 50% by weight. If this value is less than 20% by weight, not only the adhesive strength is too low, but also the required amount of polyvinyl chloride plasticizer cannot be mixed uniformly. while 50
If the amount exceeds % by weight, it is difficult to laminate the base film of the surface protection film by melt extrusion molding. Further, it is desirable that the melt index of this resin is about 2 to 50 in a state in which a plasticizer described below is mixed therein. Plasticizers for polyvinyl chloride mixed into ethylene/vinyl acetate resin include phthalic acid derivatives such as dioctyl phthalate, adipic acid derivatives such as dioctyl adipate, azelaic acid derivatives such as dioctyl azelate, and dioctyl sebacate. sebacic acid derivatives, maleic acid derivatives such as dioctyl maleate, fumaric acid, trimellitic acid, citric acid, itaconic acid,
Among compounds that can be used as plasticizers for polyvinyl chloride, such as derivatives of oleic acid, ricinoleic acid, stearic acid, various sulfonic acids, phosphoric acid, and glycolic acid, those that are liquid at room temperature are used. Monomethyl itaconate, diethylene glycol distearate, and the like, which are solid at room temperature, have no effect when used for reasons that are unclear. The mixing effect is greatest when the plasticizer is the same as the plasticizer most abundantly contained in cosmetic PVC sheets (so-called primary plasticizer), but it does not have to be the same. The mixing ratio of plasticizer to ethylene/vinyl acetate copolymer resin is 2 to 30
% by weight, preferably 5-15% by weight. The polyolefin film used as the base material of the surface protection film has a melt index of 2 to 2.
50 (preferably 6 to 15) low-density polyethylene and medium-density polyethylene are preferred from the viewpoint of physical properties. The adhesive force between the surface protection film and the decorative board is generally about 50 to 200g/25mm (at most 500g/25mm).
mm) is considered appropriate, and the adhesion conditions will be changed depending on the characteristics of the adhesive so that the decorative board of the present invention has an adhesive force within the above range, but as long as there is no risk of natural peeling. , there is no problem even if the adhesive force is lowered to about 20g/25mm. In the decorative board of the present invention, the decorative PVC sheet and the steel plate, wood plywood, etc. to which it is adhered are:
It is not limited in any way. The decorative board of the present invention as described above uses a polyolefin film as the base material of the surface protection film and an ethylene/vinyl acetate copolymer resin mixed with a plasticizer for polyvinyl chloride as an adhesive. Although the mechanism of action of the agent has not yet been confirmed, the adhesion of the protective film is stable for a long time, and therefore the protective film does not peel off naturally even under harsh conditions, and the protective film does not peel off after being peeled off. No adhesive from the film will remain and stain the surface of the decorative board. Furthermore, the protective film after being removed from the decorative board has the advantage of being easy to dispose of, as the adhesive layer is non-stick and does not generate corrosive or irritating gases even when incinerated. . The decorative laminate of the present invention may be manufactured by a conventional method in which a PVC decorative laminate is manufactured and then a surface protection film is bonded to the plate, but a particularly advantageous manufacturing method is the manufacturing method according to the present invention as detailed below. It is. In the manufacturing method of the present invention, as shown in FIG. 1, a laminated sheet is prepared in which a surface protection film 2 is adhered in advance to a decorative PVC sheet 1 to be adhered to a substrate such as a steel plate or wood plywood. However, numeral 3 in the figure is an adhesive layer of the above composition for use as a protective film, 1a is a surface that becomes the surface of the decorative board, and 1b is a surface that is bonded to the substrate. This laminated sheet may be manufactured by any method, but the following are particularly preferable because there is little strain left in the laminated sheet and it is less likely to spontaneously peel off even with low adhesive strength. It is manufactured by a method such as That is, the polyolefin resin that serves as the base material of the surface protection film and the adhesive component are heated and melted in separate extruders, and then the melts are combined into a layer and extruded through a T-die to form a film by a so-called co-extrusion method. The resulting laminate of polyolefin and adhesive, while still in a molten state, is pressed onto a decorative PVC sheet in the arrangement shown in FIG. In the manufacturing method of the present invention, a laminated sheet as shown in Fig. 1 is adhered to a substrate such as steel or wood plywood with surface 1b as the adhesive surface. You can do it in the same way as in the case. FIG. 2 shows the decorative board of the present invention made in this manner, where 4 is a substrate and 5 is an adhesive used to bond the laminated sheet of FIG. 1 to the substrate 4. The advantages of the manufacturing method of the present invention as described above are as follows. Since the decorative PVC sheet is already protected by a protective film at the time it is bonded to the substrate, surface damage during the bonding process can be avoided. In order to adhere a heat-sensitive surface protection film to a PVC decorative board using the conventional method, the entire decorative board, which has a large heat capacity, must be heated to a temperature that can be bonded, which not only consumes a large amount of heat but also makes uniform heating difficult. Therefore, there was a problem in that adhesive strength was likely to be uneven. In the case of PVC steel plates, there is a method to reduce heat consumption by adhering a surface protection film immediately after adhering the PVC sheet to the steel plate in a heated state, but in this case too, adhesion spots may occur due to temperature unevenness. This is unavoidable, and the adhesion conditions are restricted due to the process of adhering the protective film being incorporated into the PVC steel sheet production line. Therefore, the advantage of the heat-sensitive type is that the adhesion force can be adjusted by changing the heating temperature and pressure bonding time. do not have.
In contrast, in the method of the present invention, the protective film, which requires delicate adjustment of adhesive strength, is bonded to the thin PVC sheet before being bonded to the substrate, so all the drawbacks of the conventional method described above are avoided. It will be resolved. Previous attempts have been made to bond a heat-sensitive surface protection sheet to a decorative PVC sheet before adhering it to a substrate to create a laminated sheet, but this method allows the adhesive to be bonded by the transfer of plasticizer in the PVC sheet immediately after lamination. However, the method of the present invention has the drawback that the adhesion strength of the protective film on the product varies depending on the length of storage period in the laminated sheet state as the adhesive strength begins to decrease, making it impractical. This problem has been solved by using a unique adhesive that exhibits very little reduction in adhesive strength. The present invention will be explained below with reference to Examples. The adhesive strength shown in Table 1 is for a sample with a width of 25 mm.
Tensile speed 300mm/min, peel angle 180゜, 23℃・65%RH
Measured using Toyo Baldwin Tensilon under the following conditions. Example 1 Base material: polyethylene with a density of 0.920 and MI10. Adhesive: MI5 ethylene/vinyl acetate copolymer resin with vinyl acetate content of 28% by weight and 10% by weight of dioctyl phthalate. The above materials for surface protection films are co-extruded into laminates with a thickness of 50 μm for the former and 20 μm for the latter, and while they are still in a molten state, a PVC sheet (as a plasticizer) is containing dioctyl phthalate) with the adhesive layer on the inside. At that time, eight types of laminated sheets (a
-h) were produced. Each laminated sheet was stored at room temperature for 30 days and then bonded to a steel plate to produce a PVC steel plate. No peeling occurred. Example 2 Base material: polyethylene with a density of 0.924 and MI10. Adhesive: MI5 ethylene/vinyl acetate copolymer with a vinyl acetate content of 20% by weight and 5% by weight of dioctyl adipate. The above materials for the surface protection film were prepared in the same manner as in Example 1, with the former having a thickness of 30 μm and the latter having a thickness of 30 μm.
A laminate with a thickness of 40 μm is formed and is further pressure-bonded to a PVC sheet containing dioctyl phthalate. At that time, by changing the pressure bonding conditions, two types of laminated sheets (i,
j) was manufactured. After storing each laminated sheet at room temperature for 30 days, it was adhered to plywood to produce decorative PVC plywood. During adhesion and cutting of the obtained decorative plywood, natural peeling of the surface protection film did not occur. Example 3 Base material: polyethylene with a density of 0.918 and MI10. Adhesive: 45% by weight of vinyl acetate, MI2 ethylene/vinyl acetate copolymer resin mixed with 20% by weight of dioctyl phthalate. The above materials for the surface protection film were prepared in the same manner as in Example 1, with the former having a thickness of 40 μm and the latter having a thickness of 40 μm.
A laminate with a thickness of 30μ is formed, and is further pressure-bonded to a PVC sheet containing dioctyl phthalate. At that time, by changing the pressure bonding conditions, two types of laminated sheets (k,
l) was produced. The obtained laminated sheet was then adhered to a steel plate to produce a PVC steel plate. [Comparative Test of Adhesive Strength] Table 1 shows the results of examining the adhesive strength between the protective film and the cosmetic PVC sheet and its change over time for the products according to each of the above examples. However, for convenience, the test was conducted on a laminated sheet that was not adhered to a substrate, and the change over time was accelerated by applying a load of 10 g/cm 2 and heating to 40°C or 65°C. Comparative Examples 1 and 2 shown in the table were manufactured by the same manufacturing method as each Example and had the following configuration. Protective film base material: Same as Example 1. Adhesive: MI5 ethylene/vinyl acetate copolymer resin with vinyl acetate content of 28% by weight. Layer thickness 20μ. PVC sheet: Same as Example 1.

【表】 第1表から明らかなように、加熱促進試験によ
り比較例のものはまつたく接着力を失なつたのに
対し、本発明のものは、初期強度がかなり小さい
ものでも、なお自然剥離を起こさない程度の接着
力を維持していた。また接着力測定後に塩ビシー
トの表面を観察したが、汚れ等はまつたく認めら
れなかつた。
[Table] As is clear from Table 1, in the accelerated heating test, the comparative example quickly lost its adhesive strength, whereas the inventive product still peeled naturally even though its initial strength was quite low. The adhesion strength was maintained to the extent that no damage was caused. Furthermore, when the surface of the PVC sheet was observed after measuring the adhesive strength, no stains or the like were observed at all.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は本発明の化粧板を製造するのに用いる
積層シートの断面図、第2図は第1図の積層シー
トを用いて作られた本発明の化粧板の断面図であ
る。 1:化粧用塩ビシート、2:表面保護フイル
ム、3,5:接着剤層、4:基板。
FIG. 1 is a sectional view of a laminated sheet used to manufacture the decorative laminate of the present invention, and FIG. 2 is a sectional view of the decorative laminate of the present invention made using the laminated sheet of FIG. 1. 1: Decorative PVC sheet, 2: Surface protection film, 3, 5: Adhesive layer, 4: Substrate.

Claims (1)

【特許請求の範囲】 1 鋼板又は木質合板からなる基板、基板の少な
くとも1面に接着された化粧用ポリ塩化ビニルシ
ート、及び化粧用ポリ塩化ビニルシートに剥離可
能な程度に接着された表面保護用ポリオレフイン
フイルムよりなり、ポリオレフインフイルムは常
温で液体のポリ塩化ビニル用可塑剤を混入したエ
チレン−酢酸ビニル共重合樹脂により化粧用ポリ
塩化ビニルシートに接着されていることを特徴と
する表面保護シート付化粧板。 2 鋼板又は木質合板からなる基板に化粧用ポリ
塩化ビニルシートが接着され更に表面保護フイル
ムが剥離可能な程度に接着された化粧板を製造す
るに当り、表面保護用ポリオレフインフイルムが
常温で液体のポリ塩化ビニル用可塑剤を混入した
エチレン−酢酸ビニル共重合樹脂によりあらかじ
め化粧用ポリ塩化ビニルシートに接着されてなる
積層シートの形で化粧用ポリ塩化ビニルシートを
基板に接着することを特徴とする表面化粧板の製
造法。
[Scope of Claims] 1. A substrate made of a steel plate or wood plywood, a decorative polyvinyl chloride sheet adhered to at least one surface of the substrate, and a surface protection sheet adhered to the decorative polyvinyl chloride sheet to a peelable extent. A cosmetic with a surface protection sheet, which is made of a polyolefin in-film, and the polyolefin in-film is adhered to a cosmetic polyvinyl chloride sheet using an ethylene-vinyl acetate copolymer resin mixed with a plasticizer for polyvinyl chloride, which is liquid at room temperature. Board. 2. When manufacturing a decorative board in which a decorative polyvinyl chloride sheet is adhered to a substrate made of steel plate or wood plywood, and a surface protection film is further adhered to such an extent that it can be peeled off, the surface protection polyolefin film is a liquid polyvinyl chloride sheet at room temperature. A surface characterized by adhering a decorative polyvinyl chloride sheet to a substrate in the form of a laminated sheet, which has been previously adhered to the decorative polyvinyl chloride sheet with an ethylene-vinyl acetate copolymer resin mixed with a plasticizer for vinyl chloride. Manufacturing method of decorative board.
JP16581581A 1981-10-19 1981-10-19 Decorative board and its manufacture Granted JPS5867444A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP16581581A JPS5867444A (en) 1981-10-19 1981-10-19 Decorative board and its manufacture

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP16581581A JPS5867444A (en) 1981-10-19 1981-10-19 Decorative board and its manufacture

Publications (2)

Publication Number Publication Date
JPS5867444A JPS5867444A (en) 1983-04-22
JPH0137266B2 true JPH0137266B2 (en) 1989-08-04

Family

ID=15819516

Family Applications (1)

Application Number Title Priority Date Filing Date
JP16581581A Granted JPS5867444A (en) 1981-10-19 1981-10-19 Decorative board and its manufacture

Country Status (1)

Country Link
JP (1) JPS5867444A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2683562B2 (en) * 1988-06-22 1997-12-03 大日本印刷株式会社 Method of preventing retransfer of diallyl phthalate resin entrained embossed decorative board
JPH0379930U (en) * 1989-12-05 1991-08-15

Also Published As

Publication number Publication date
JPS5867444A (en) 1983-04-22

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