JPH0257767B2 - - Google Patents
Info
- Publication number
- JPH0257767B2 JPH0257767B2 JP6806583A JP6806583A JPH0257767B2 JP H0257767 B2 JPH0257767 B2 JP H0257767B2 JP 6806583 A JP6806583 A JP 6806583A JP 6806583 A JP6806583 A JP 6806583A JP H0257767 B2 JPH0257767 B2 JP H0257767B2
- Authority
- JP
- Japan
- Prior art keywords
- sheet
- pattern
- resin
- ink
- printed pattern
- 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
Links
- 229920005989 resin Polymers 0.000 claims description 30
- 239000011347 resin Substances 0.000 claims description 30
- 238000010438 heat treatment Methods 0.000 claims description 6
- 230000001678 irradiating effect Effects 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 229920005992 thermoplastic resin Polymers 0.000 claims description 2
- 239000000976 ink Substances 0.000 description 18
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 13
- 238000000034 method Methods 0.000 description 11
- -1 polyethylene Polymers 0.000 description 5
- 239000003085 diluting agent Substances 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 3
- 229910052753 mercury Inorganic materials 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- 239000011342 resin composition Substances 0.000 description 3
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- YNSNJGRCQCDRDM-UHFFFAOYSA-N 1-chlorothioxanthen-9-one Chemical compound S1C2=CC=CC=C2C(=O)C2=C1C=CC=C2Cl YNSNJGRCQCDRDM-UHFFFAOYSA-N 0.000 description 1
- PIZHFBODNLEQBL-UHFFFAOYSA-N 2,2-diethoxy-1-phenylethanone Chemical compound CCOC(OCC)C(=O)C1=CC=CC=C1 PIZHFBODNLEQBL-UHFFFAOYSA-N 0.000 description 1
- NLGDWWCZQDIASO-UHFFFAOYSA-N 2-hydroxy-1-(7-oxabicyclo[4.1.0]hepta-1,3,5-trien-2-yl)-2-phenylethanone Chemical compound OC(C(=O)c1cccc2Oc12)c1ccccc1 NLGDWWCZQDIASO-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000004049 embossing Methods 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 229920006158 high molecular weight polymer Polymers 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000010297 mechanical methods and process Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000001360 synchronised effect Effects 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-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
- B29C59/00—Surface shaping of articles, e.g. embossing; Apparatus therefor
-
- 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
- B29C35/00—Heating, cooling or curing, e.g. crosslinking or vulcanising; Apparatus therefor
- B29C35/02—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould
- B29C35/08—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould by wave energy or particle radiation
-
- 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
- B29C55/00—Shaping by stretching, e.g. drawing through a die; Apparatus therefor
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
- B29L2031/00—Other particular articles
- B29L2031/722—Decorative or ornamental articles
Landscapes
- Shaping Of Tube Ends By Bending Or Straightening (AREA)
- Shaping By String And By Release Of Stress In Plastics And The Like (AREA)
Description
本発明は、表面に施された印刷模様と完全に同
調した凹凸模様を有するシートを製造する方法に
関する。
従来、家具、建具或いは電気機器外装板等とし
て、その表面に木目や幾何学的な凹凸模様を付し
た樹脂装飾シートが広く用いられているが、これ
らのシートは多くの場合、エンボシングによつて
製造されている。しかし、このような機械的な方
法によれば、シートの有する模様と厳密に同調し
た凹凸の模様付けを行なうことは困難であるほ
か、多数の大型の設備を要して製造費用が嵩む問
題がある。
本発明は上記した問題を解決するためになされ
たものであつて、簡単でありながら、印刷模様と
完全に同調した凹凸模様を有する樹脂シートの製
造方法を提供することを目的とする。
本発明による樹脂シートの製造方法は、熱可塑
性樹脂シートの表面に紫外線硬化性樹脂インキに
て所要形状に模様を印刷し、紫外線を照射した
後、加熱延伸して、上記樹脂シート表面に印刷模
様に同調した凹凸模様を形成させることを特徴と
する。
以下に実施例を示す図面に基づいて本発明を説
明する。
第1図は、加熱延伸前の基材樹脂シート1を示
す。基材シートは、特に制限されないが、例え
ば、ポリ塩化ビニル樹脂、ポリエチレン、ポリプ
ロピレン、エチレン−酢酸ビニル共重合体、ポリ
酢酸ビニル、飽和ポリエステル、ポリ塩化ビニリ
デン、アクリル樹脂、熱可塑性ポリウレタン樹脂
等が用いられる。基材シートは樹脂に応じて必要
な各種添加剤、例えば、可塑剤、充填剤、着色
剤、酸化防止剤その他を含有していてもよい。
このような基材シートの厚みは、後述するよう
に、基材シートを加熱延伸したときに、シートが
非印刷部分で延伸され、印刷部分で有効に隆起し
て、所要の凹凸模様を形成することができるよう
に、通常、0.05〜1mm程度であることがが好まし
い。
本発明の方法によれば、このような基材樹脂シ
ートの表面に紫外線硬化性樹脂インキ2にて所要
の模様を印刷する。印刷模様の厚みは、この印刷
インキを架橋させた後に加熱延伸した際に、シー
トの印刷模様部分が実質的に延伸されないように
選ばれる。
本発明の方法において用いる紫外線硬化性樹脂
インキは、通常、塗膜形成性成分、反応性希釈剤
及び光重合開始剤を含有し、必要に応じて溶剤、
染顔料、充填剤等を含有してなり、紫外線照射に
より通常数秒以内に架橋硬化する樹脂組成物から
なるインキである。塗膜形成性成分には通常、ア
クリロイル基やメタクリロイル基或いはその他の
付加重合性二重結合を分子内に有する高分子重合
体、オリゴマー、モノマー等が用いられる。本発
明においては、かかる塗膜形成性成分として、ポ
リエステル(メタ)アクリレートウレタン(メ
タ)アクリレート、エポキシ(メタアクリレート
等が好ましく用いられる。
反応性希釈剤は、上記塗膜形成性成分の粘度を
低下させて、印刷適性を有せしめると共に、紫外
線照射を受けて塗膜形成性成分を架橋網状化させ
ために配合されるもので、通常、多官能性のオリ
ゴマー又はモノマーである。本発明においてはか
かる反応性希釈剤として、分子内に2個以上のア
クリレート基及び/又はメタクリレート基を有す
るモノマーが好ましく用いられ、これらの具体例
として、例えば、トリメチロールプロパントリ
(メタ)アクリレート、ペンタエリスリトールト
リ(メタ)アクリレート、ブタンジオールジ(メ
タ)アクリレート、ネオペンチルグリコールジ
(メタ)アクリレート、1,6−ヘキサンジオー
ルジ(メタ)アクリレート、ジエチレングリコー
ルジ(メタ)アクリレート等を挙げることができ
る。更に、これらに2−エチルヘキシル(メタ)
アクリレート、2−ヒドロキシエチル(メタ)ア
クリレート、グリシジル(メタ)アクリレートN
−ビニル−2−ピロリドン、テトラヒドロフルフ
リル(メタ)アクリレート等の単官能性モノマー
を併用することができる。また、光重合開始剤と
しては、通常、ベンジル、ベンゾフエノン、ベン
ゾインエーテル、クロロチオキサントン、ジエト
キシアセトフエノン、ベンジルジメチルケタール
等が用いられる。
上記のような紫外線硬化性樹脂インキにおける
各成分の配合量は、通常、塗膜形成性成分が約20
〜90重量%、好ましくは40〜70重量%、反応性希
釈剤が約10〜80重量%、好ましくは30〜60重量
%、光重合開始剤が約0.5〜10重量%であり、必
要に応じて前記したような成分が更に配合され
る。
次いで、本発明によれば、シートの上記印刷模
様面から紫外線を照射し、印刷模様を架橋硬化さ
せる。インキを架橋硬化させる方法は、従来より
知られている普通の方法によればよく、例えば、
キセノンランプ、低圧、中圧、高圧或いは超高圧
水銀灯のような紫外線源を使用すればよい。紫外
線は、紫外線硬化性樹脂インキが十分に硬化する
に足る量を照射すればよく、インキに応じて適宜
に選ばれが、一例として主波長が365mμ、出力
80W/cmの水銀灯の場合、1秒間乃至数秒間照射
すればよい。
この後にシートを加熱延伸すると、第2図に示
すように、基材シートは、表面に印刷模様を有し
ないシート部分のみが実質的に延伸され、一方、
表面に印刷模様を有するシート部分はインキが架
橋硬化しているために実質的に延伸されず、かく
して、印刷模様を有するシート部分がシート表面
から隆起して、印刷模様に完全に同調した凹凸模
様を形成する。上記シートの加熱温度は、通常、
100〜200℃の範囲が適当であり、また、延伸率は
縦横共に5〜40%が適当である。尚、縦横共にほ
ぼ同じ延伸率で延伸されるのが望ましい。この加
熱温度及び延伸率によつて、印刷模様を表面に有
しないシート部分の延伸を制御して、印刷模様を
有するシート部分の隆起高さを制御することがで
きる。
第3図は本発明の方法の別の実施例において、
加熱前の積層された基材シートを示す。即ち、紫
外線硬化性樹脂インキ2にて印刷模様を付した基
材シート1を前記と同様にその表面から紫外線を
照射した後、その裏面に別の樹脂シート、例え
ば、塩化ビニル樹脂シート3をラミネーシヨン等
の法により貼着積層し、この後にシートを加熱延
伸することにより、第4図に示すように、前記樹
脂シート3も基材シート1が非印刷模様部分にお
いて延伸されるのに追随して延伸され、かくし
て、印刷模様に完全に同調して凹凸模様を形成す
る。上記樹脂シート3に着色シートを用いると
き、このシートを印刷模様の背景とすることがで
きる。
以上のように、本発明の方法によれば、延伸し
得る基材シートに所要の模様を紫外線硬化性樹脂
インキにて印刷し、その印刷模様面に紫外線を照
射して架橋硬化させた後、基材シートを加熱延伸
するので、表面に架橋したインキによる模様を有
しないシート部分のみが実質的に延伸され、一
方、表面に印刷模様を有する部分を実質的に延伸
されず、この結果、この部分がシート表面に隆起
して、印刷模様に完全に同調した凹凸模様を形成
する。
以下に実施例を挙げて本発明を説明するが、本
発明はこれら実施例により何ら限定されるもので
はない。
実施例 1
平均重合度1100の塩化ビニル樹脂100重量部に
ついて通常の可塑剤12重量部及び適宜量の安定剤
と顔料とを含有する樹脂組成物をカレンダー法に
て厚み0.075mmのシートに成形した。
この基材シートの表面に表に示す組成の紫外線
硬化性樹脂インキA乃至Cをそれぞれ用いて木目
模様を印刷し、主波長356mμ、出力80W/cmの水
銀灯を用いて紫外線を1秒間照射した後、170℃
の温度で縦横共に15%の延伸率で延伸
The present invention relates to a method for producing a sheet having an uneven pattern that is completely in sync with a printed pattern on the surface. Conventionally, resin decorative sheets with wood grain or geometric uneven patterns on the surface have been widely used as exterior panels for furniture, fittings, or electrical equipment, but these sheets are often decorated with embossing. Manufactured. However, with such mechanical methods, it is difficult to create an uneven pattern that closely matches the pattern of the sheet, and there is also the problem that it requires a large number of large equipment, which increases manufacturing costs. be. The present invention has been made in order to solve the above-mentioned problems, and an object of the present invention is to provide a simple method for manufacturing a resin sheet having a concavo-convex pattern that is completely in sync with a printed pattern. The method for manufacturing a resin sheet according to the present invention includes printing a pattern in a desired shape on the surface of a thermoplastic resin sheet using ultraviolet curable resin ink, irradiating it with ultraviolet rays, and then heating and stretching the resin sheet to print the pattern on the surface of the resin sheet. It is characterized by forming a concavo-convex pattern that is synchronized with the . The present invention will be described below based on drawings showing examples. FIG. 1 shows a base resin sheet 1 before being heated and stretched. The base sheet is not particularly limited, but for example, polyvinyl chloride resin, polyethylene, polypropylene, ethylene-vinyl acetate copolymer, polyvinyl acetate, saturated polyester, polyvinylidene chloride, acrylic resin, thermoplastic polyurethane resin, etc. can be used. It will be done. The base sheet may contain various necessary additives depending on the resin, such as plasticizers, fillers, colorants, antioxidants, and the like. The thickness of such a base sheet is such that when the base sheet is heated and stretched, the non-printing part of the sheet is stretched and the printed part is effectively raised to form the desired uneven pattern. Generally, the thickness is preferably about 0.05 to 1 mm. According to the method of the present invention, a desired pattern is printed on the surface of such a base resin sheet using ultraviolet curable resin ink 2. The thickness of the printed pattern is selected so that when the printing ink is crosslinked and then heated and stretched, the printed pattern portion of the sheet is not substantially stretched. The ultraviolet curable resin ink used in the method of the present invention usually contains a film-forming component, a reactive diluent, and a photopolymerization initiator, and if necessary, a solvent,
It is an ink made of a resin composition that contains dyes, pigments, fillers, etc., and is usually crosslinked and cured within a few seconds when exposed to ultraviolet rays. High molecular weight polymers, oligomers, monomers, etc. having an acryloyl group, a methacryloyl group, or other addition-polymerizable double bonds in the molecule are usually used as the film-forming component. In the present invention, polyester (meth)acrylate, urethane (meth)acrylate, epoxy (methacrylate, etc.) are preferably used as the film-forming component.The reactive diluent reduces the viscosity of the film-forming component. It is blended to make the coating film-forming component cross-linked and networked by UV irradiation, and is usually a polyfunctional oligomer or monomer. As the reactive diluent, monomers having two or more acrylate groups and/or methacrylate groups in the molecule are preferably used, and specific examples thereof include trimethylolpropane tri(meth)acrylate, pentaerythritol tri(meth) ) acrylate, butanediol di(meth)acrylate, neopentyl glycol di(meth)acrylate, 1,6-hexanediol di(meth)acrylate, diethylene glycol di(meth)acrylate, and the like. -ethylhexyl (meth)
Acrylate, 2-hydroxyethyl (meth)acrylate, glycidyl (meth)acrylate N
Monofunctional monomers such as -vinyl-2-pyrrolidone and tetrahydrofurfuryl (meth)acrylate can be used in combination. Further, as the photopolymerization initiator, benzyl, benzophenone, benzoin ether, chlorothioxanthone, diethoxyacetophenone, benzyl dimethyl ketal, etc. are usually used. The blending amount of each component in the above-mentioned ultraviolet curable resin ink is usually about 20% of the film-forming component.
-90% by weight, preferably 40-70% by weight, reactive diluent about 10-80% by weight, preferably 30-60% by weight, photoinitiator about 0.5-10% by weight, optionally The above-mentioned components are further blended. Next, according to the present invention, ultraviolet rays are irradiated from the printed pattern surface of the sheet to crosslink and cure the printed pattern. The method for crosslinking and curing the ink may be any conventionally known method, for example,
UV light sources such as xenon lamps, low pressure, medium pressure, high pressure or extra high pressure mercury lamps may be used. The amount of ultraviolet rays that is sufficient to fully cure the ultraviolet curable resin ink can be selected depending on the ink.
In the case of an 80W/cm mercury lamp, irradiation can be performed for one to several seconds. When the sheet is then heated and stretched, only the portion of the base sheet that does not have a printed pattern on its surface is substantially stretched, as shown in FIG.
The sheet portion having the printed pattern on its surface is not substantially stretched because the ink has been cross-linked and cured, and thus the sheet portion having the printed pattern rises from the sheet surface, creating an uneven pattern that perfectly matches the printed pattern. form. The heating temperature of the above sheet is usually
A suitable temperature range is 100 to 200°C, and a suitable stretching ratio is 5 to 40% in both length and width. Note that it is desirable that the film be stretched at approximately the same stretching rate in both length and width. By controlling the heating temperature and stretching rate, it is possible to control the stretching of the sheet portion that does not have a printed pattern on its surface, and to control the height of the protrusion of the sheet portion that has a printed pattern. FIG. 3 shows, in another embodiment of the method of the invention,
The laminated base sheets are shown before heating. That is, after irradiating the surface of a base sheet 1 with a printed pattern using ultraviolet curable resin ink 2 with ultraviolet rays in the same manner as described above, another resin sheet, for example, a vinyl chloride resin sheet 3, is laminated on the back surface of the base sheet 1. By adhering and laminating the sheets by the method of Shion et al., and then heating and stretching the sheets, the resin sheet 3 follows the stretching of the base sheet 1 in the non-printed pattern area, as shown in FIG. and is stretched, thus forming an uneven pattern in perfect synchronization with the printed pattern. When a colored sheet is used as the resin sheet 3, this sheet can be used as a background of a printed pattern. As described above, according to the method of the present invention, a desired pattern is printed on a stretchable base sheet using ultraviolet curable resin ink, and the printed pattern surface is crosslinked and cured by irradiating ultraviolet rays. Since the base sheet is heated and stretched, only the portion of the sheet that does not have a cross-linked ink pattern on its surface is substantially stretched, while the portion that has a printed pattern on its surface is not substantially stretched. The areas are raised on the surface of the sheet, forming an uneven pattern that perfectly matches the printed pattern. The present invention will be explained below with reference to Examples, but the present invention is not limited to these Examples in any way. Example 1 A resin composition containing 100 parts by weight of vinyl chloride resin with an average degree of polymerization of 1100, 12 parts by weight of a conventional plasticizer, and appropriate amounts of stabilizers and pigments was molded into a sheet with a thickness of 0.075 mm by a calendar method. . After printing a wood grain pattern on the surface of this base sheet using ultraviolet curable resin inks A to C having the compositions shown in the table, and irradiating it with ultraviolet rays for 1 second using a mercury lamp with a dominant wavelength of 356 mμ and an output of 80 W/cm, ,170℃
Stretched at a temperature of 15% in both length and width.
【表】【table】
【表】
して、いずれのインキを用いた場合にも、印刷模
様部分に同調して凸模様が形成されたシートを得
ることができた。
実施例 2
実施例1で得た印刷済みのシートを同様に紫外
線照射した。別に、平均重合度1100の塩化ビニル
樹脂100重量部について、通常の可塑剤17重量部
及び適宜量の安定剤、顔料及び充填剤とを含有す
る樹脂組成物をカレンダー法にて厚み0.1mmのシ
ートに成形し、これを上記基材シートの裏面にラ
ミネーシヨンした。次いで、この積層シートを
170℃の温度で縦横共に15%の延伸率で延伸して、
いずれのインキを用いた場合にも、印刷模様部分
に同調して凸模様が形成されたシートを得ること
ができた。[Table] No matter which ink was used, it was possible to obtain a sheet in which a convex pattern was formed in synchronization with the printed pattern portion. Example 2 The printed sheet obtained in Example 1 was similarly irradiated with ultraviolet rays. Separately, a resin composition containing 100 parts by weight of vinyl chloride resin with an average degree of polymerization of 1100, 17 parts by weight of a normal plasticizer, and appropriate amounts of stabilizers, pigments, and fillers was prepared by calendering into a sheet with a thickness of 0.1 mm. This was then laminated on the back side of the base sheet. Next, this laminated sheet
Stretched at a temperature of 170°C with a stretching ratio of 15% in both the length and width,
No matter which ink was used, it was possible to obtain a sheet in which a convex pattern was formed in synchronization with the printed pattern portion.
図面は本発明による方法の実施例を示し、第1
図は紫外線硬化性樹脂インキによる印刷模様を表
面に有する基材シートの要部断面図、第2図は第
1図のシートから得られる本発明による凹凸模様
を有するシートの要部断面図、第3図は例えば着
色樹脂シートを積層した基材シートの断面図、第
4図は第3図のシートから得られる本発明による
凹凸模様を有するシートの断面図である。
1……基材シート、2……紫外線硬化性樹脂イ
ンキ、3……樹脂シート。
The drawing shows an embodiment of the method according to the invention, in which the first
The figure is a cross-sectional view of a main part of a base sheet having a pattern printed with ultraviolet curable resin ink on its surface, FIG. FIG. 3 is a sectional view of a base sheet laminated with, for example, colored resin sheets, and FIG. 4 is a sectional view of a sheet having an uneven pattern according to the present invention obtained from the sheet of FIG. 3. 1... Base material sheet, 2... Ultraviolet curable resin ink, 3... Resin sheet.
Claims (1)
脂インキにて所要形状に模様を印刷し、紫外線を
照射した後、加熱延伸して、上記樹脂シート表面
に印刷模様に同調した凹凸模様を形成させること
を特徴とする樹脂シートの製造方法。1. Printing a pattern in a desired shape on the surface of a thermoplastic resin sheet using ultraviolet curable resin ink, irradiating it with ultraviolet rays, and then heating and stretching to form an uneven pattern on the surface of the resin sheet that matches the printed pattern. A method for producing a resin sheet characterized by:
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6806583A JPS59192531A (en) | 1983-04-18 | 1983-04-18 | Manufacturing method of resin sheet |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6806583A JPS59192531A (en) | 1983-04-18 | 1983-04-18 | Manufacturing method of resin sheet |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59192531A JPS59192531A (en) | 1984-10-31 |
| JPH0257767B2 true JPH0257767B2 (en) | 1990-12-05 |
Family
ID=13362999
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP6806583A Granted JPS59192531A (en) | 1983-04-18 | 1983-04-18 | Manufacturing method of resin sheet |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59192531A (en) |
-
1983
- 1983-04-18 JP JP6806583A patent/JPS59192531A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS59192531A (en) | 1984-10-31 |
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