JPH0132791B2 - - Google Patents
Info
- Publication number
- JPH0132791B2 JPH0132791B2 JP56149050A JP14905081A JPH0132791B2 JP H0132791 B2 JPH0132791 B2 JP H0132791B2 JP 56149050 A JP56149050 A JP 56149050A JP 14905081 A JP14905081 A JP 14905081A JP H0132791 B2 JPH0132791 B2 JP H0132791B2
- Authority
- JP
- Japan
- Prior art keywords
- heat
- foamable
- pattern
- printing
- ink
- 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
- 239000000463 material Substances 0.000 claims description 42
- 238000005187 foaming Methods 0.000 claims description 28
- 239000000758 substrate Substances 0.000 claims description 11
- 239000006260 foam Substances 0.000 claims description 8
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 238000010438 heat treatment Methods 0.000 claims description 6
- 230000001629 suppression Effects 0.000 claims description 5
- 230000000994 depressogenic effect Effects 0.000 claims description 2
- 238000007639 printing Methods 0.000 description 40
- 239000000123 paper Substances 0.000 description 35
- 239000000976 ink Substances 0.000 description 32
- 238000000034 method Methods 0.000 description 26
- 239000010410 layer Substances 0.000 description 18
- 238000000576 coating method Methods 0.000 description 16
- 229920005989 resin Polymers 0.000 description 16
- 239000011347 resin Substances 0.000 description 16
- 239000011248 coating agent Substances 0.000 description 13
- 239000003981 vehicle Substances 0.000 description 13
- -1 polyethylene Polymers 0.000 description 12
- 239000004088 foaming agent Substances 0.000 description 11
- 239000004800 polyvinyl chloride Substances 0.000 description 8
- 229920000915 polyvinyl chloride Polymers 0.000 description 8
- 238000007646 gravure printing Methods 0.000 description 7
- 239000003973 paint Substances 0.000 description 7
- 239000000049 pigment Substances 0.000 description 6
- 239000004014 plasticizer Substances 0.000 description 6
- 239000011342 resin composition Substances 0.000 description 6
- 239000003381 stabilizer Substances 0.000 description 6
- 239000004743 Polypropylene Substances 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 239000003112 inhibitor Substances 0.000 description 5
- 229920001155 polypropylene Polymers 0.000 description 5
- 238000007650 screen-printing Methods 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 239000000057 synthetic resin Substances 0.000 description 5
- 229920003002 synthetic resin Polymers 0.000 description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 238000007645 offset printing Methods 0.000 description 4
- 238000010023 transfer printing Methods 0.000 description 4
- 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
- 239000004156 Azodicarbonamide Substances 0.000 description 3
- 239000004606 Fillers/Extenders Substances 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- 239000004793 Polystyrene Substances 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
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 3
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 description 3
- 235000019399 azodicarbonamide Nutrition 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- 239000003085 diluting agent Substances 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000003365 glass fiber Substances 0.000 description 3
- 238000004898 kneading Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 150000007524 organic acids Chemical class 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- 229920002223 polystyrene Polymers 0.000 description 3
- 239000011241 protective layer Substances 0.000 description 3
- 239000002904 solvent 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
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- 239000004604 Blowing Agent Substances 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 229920000219 Ethylene vinyl alcohol Polymers 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000004677 Nylon Substances 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 239000012790 adhesive layer Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 238000007754 air knife coating Methods 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 230000003254 anti-foaming effect Effects 0.000 description 2
- 239000002216 antistatic agent Substances 0.000 description 2
- 239000010425 asbestos Substances 0.000 description 2
- 230000000903 blocking effect Effects 0.000 description 2
- 229920006026 co-polymeric resin Polymers 0.000 description 2
- 238000003618 dip coating Methods 0.000 description 2
- 238000007756 gravure coating Methods 0.000 description 2
- 229920000554 ionomer Polymers 0.000 description 2
- 238000007759 kiss coating Methods 0.000 description 2
- 238000007644 letterpress printing Methods 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 239000004745 nonwoven fabric Substances 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 229910052895 riebeckite Inorganic materials 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- 239000002759 woven fabric Substances 0.000 description 2
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-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
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 1
- 229920008347 Cellulose acetate propionate Polymers 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- MWRWFPQBGSZWNV-UHFFFAOYSA-N Dinitrosopentamethylenetetramine Chemical compound C1N2CN(N=O)CN1CN(N=O)C2 MWRWFPQBGSZWNV-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 229920000896 Ethulose Polymers 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- 239000001859 Ethyl hydroxyethyl cellulose Substances 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 229920001944 Plastisol Polymers 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- 229910010413 TiO 2 Inorganic materials 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 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
- 239000001099 ammonium carbonate Substances 0.000 description 1
- 235000012501 ammonium carbonate Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- MOOAHMCRPCTRLV-UHFFFAOYSA-N boron sodium Chemical compound [B].[Na] MOOAHMCRPCTRLV-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 235000019326 ethyl hydroxyethyl cellulose Nutrition 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000009408 flooring Methods 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000002655 kraft paper Substances 0.000 description 1
- 239000011133 lead Substances 0.000 description 1
- 239000002649 leather substitute 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
- 150000002689 maleic acids Chemical class 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 239000004005 microsphere Substances 0.000 description 1
- 229920006284 nylon film Polymers 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000011088 parchment paper Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 239000004999 plastisol Substances 0.000 description 1
- 239000011120 plywood Substances 0.000 description 1
- 229920001485 poly(butyl acrylate) polymer Polymers 0.000 description 1
- 229920001483 poly(ethyl methacrylate) polymer Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920006289 polycarbonate film Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000120 polyethyl acrylate Polymers 0.000 description 1
- 229920013716 polyethylene resin Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 125000006239 protecting group Chemical group 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- XJKVPKYVPCWHFO-UHFFFAOYSA-N silicon;hydrate Chemical compound O.[Si] XJKVPKYVPCWHFO-UHFFFAOYSA-N 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000010345 tape casting Methods 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical compound OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M3/00—Printing processes to produce particular kinds of printed work, e.g. patterns
- B41M3/06—Veined printings; Fluorescent printings; Stereoscopic images; Imitated patterns, e.g. tissues, textiles
Landscapes
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Textile Engineering (AREA)
- Vascular Medicine (AREA)
- Decoration By Transfer Pictures (AREA)
- Laminated Bodies (AREA)
- Molding Of Porous Articles (AREA)
- Printing Methods (AREA)
Description
【発明の詳細な説明】
本発明は転写紙及びこれを用いた化粧材の製造
法に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a transfer paper and a method for producing a decorative material using the same.
印刷の一方法として転写紙を用いて行なう転写
印刷方法は既に知られている。ごく一般的な転写
紙は基体、剥離性層及び印刷層とからなり、これ
らの他、必要に応じて保護層及び接着剤層等を設
けてなるものであつて、これらの転写紙は合皮、
軟質塩ビ、合板、陶磁器、金属、ガラス等への印
刷に用いられ、特に直接鮮明な印刷を行なうこと
が困難な素材、形状の被印刷体に印刷する場合
や、一時に印刷する数量が少なく、しかも柄数が
多い場合等には転写紙を用いる転写印刷方法は印
刷の準備時間や終了後の後始末の時間を省くこと
ができ、柄変更の際の版替えも不要であつて便利
なものである。 2. Description of the Related Art A transfer printing method using transfer paper is already known as a printing method. A very common transfer paper consists of a base, a peelable layer, and a printing layer, and in addition to these, a protective layer, adhesive layer, etc. are provided as necessary.These transfer papers are made of synthetic leather. ,
It is used for printing on soft PVC, plywood, ceramics, metal, glass, etc., especially when printing on materials and shapes that are difficult to directly print clearly, or when printing in small quantities at one time. Moreover, when there are a large number of patterns, the transfer printing method using transfer paper is convenient because it saves preparation time for printing and cleaning up after printing, and there is no need to change plates when changing patterns. It is.
従来の転写紙を用いた転写印刷方法によつて得
られる印刷物は平担な印刷が殆んどであるが、転
写印刷後被印刷体より突出した模様を得たい場合
には、かかる模様を転写紙に形成するときに固形
分の多いインキを用いるか若しくはインキ転移量
の多い印刷方式によつて印刷する等の方法により
行なうのが普通である。しかし、固形分の多いイ
ンキを用いるときはインキの粘弾性が変化して印
刷適性上好ましくなく、又、インキ転移量の多い
印刷方式、例えばシルクスクリーン印刷、凹版印
刷、版深の深いグラビア印刷等の印刷方式を用い
ときは印刷後の乾燥速度が遅くなる欠点があり、
又、転写紙が枚葉印刷方式によつて製造されて堆
積されるとき若しくは輪転方式によつて製造され
て巻取られるときには印刷模様がつぶれる、基体
が変形する等の欠点も有していた。 Most of the printed matter obtained by the transfer printing method using conventional transfer paper is a flat print, but if you want to obtain a pattern that stands out from the printing material after transfer printing, such a pattern can be transferred. This is usually done by using ink with a high solid content when forming on paper, or by printing with a printing method that transfers a large amount of ink. However, when using ink with a high solid content, the viscoelasticity of the ink changes, which is unfavorable in terms of printing suitability, and printing methods that require a large amount of ink transfer, such as silk screen printing, intaglio printing, deep gravure printing, etc. When using this printing method, there is a disadvantage that the drying speed after printing is slow.
Furthermore, when the transfer paper is manufactured by sheet-fed printing and stacked, or manufactured by rotary printing and wound up, it also has drawbacks such as the printed pattern being crushed and the substrate being deformed.
又、従来の転写紙において発泡抑制模様を設け
てなる転写紙は公知であるが、発泡の段階を制御
する事は使用する版の版深のバラツキを少なくし
て明確な段階を設け、使用するインキ中の発泡抑
制化合物の分量を制御しても、転写紙の発泡抑制
模様の発泡抑制能力を長期に渡つて維持すること
はむずかしく、しかもかかる従来の発泡抑制模様
を設けた転写紙を使用すると面積的に見て凹部を
多く有する化粧材を製造するときには高価な発泡
抑制化合物を多量使用して転写紙を製造する必要
があり、しかも得られる転写紙は巻取つた後ブロ
ツキングしやすいという欠点をも有し凸部の面積
の少ない模様には適さず、しかも上記転写紙を利
用しても、発泡後の表面より窪んだ凹部を生じる
ことは出来ても、発泡後の表面より突出した凸部
を設けることは出来なかつた。 In addition, conventional transfer paper with a foam-suppressing pattern is known, but controlling the stage of foaming reduces the variation in the plate depth of the plates used and provides a clear stage for use. Even if the amount of the foam-suppressing compound in the ink is controlled, it is difficult to maintain the foam-suppressing ability of the foam-suppressing pattern of the transfer paper over a long period of time. When producing a decorative material that has many concave areas in terms of area, it is necessary to use a large amount of an expensive foaming-inhibiting compound to produce transfer paper, and the resulting transfer paper has the disadvantage of being prone to blocking after being rolled up. It is not suitable for patterns with a small area of convex parts, and even if the above-mentioned transfer paper is used, it is possible to create concave parts that are concave from the surface after foaming, but it is not suitable for patterns with convex parts that protrude from the surface after foaming. It was not possible to set up a
本発明は特許請求の範囲の欄の構成とすること
により、上記従来の転写紙の欠点を解消し、又、
凸部及び凹部を有する発泡化粧材を得ることに成
功したものである。 The present invention solves the above-mentioned drawbacks of the conventional transfer paper by configuring the scope of claims, and
We succeeded in obtaining a foamed decorative material having convex portions and concave portions.
以下、本発明について詳細に説明する。 The present invention will be explained in detail below.
本発明において使用する基体、剥離性層、通常
の印刷層及びその他の印刷層、保護層及び接着剤
層はいずれも公知のものを使用しうる。 Known substrates, releasable layers, ordinary printed layers, other printed layers, protective layers, and adhesive layers may be used in the present invention.
まず基体としては、薄葉紙、硫酸紙、クラフト
紙等の紙、ポリエチレンフイルム、ポリプロピレ
ンフイルム、ポリ塩化ビニルフイルム、ポリ塩化
ビニリデンフイルム、ポリビニルアルコールフイ
ルム、ポリエチレンテレフタレートフイルム、ポ
リカーボネートフイルム、ナイロンフイルム、ポ
リスチレンフイルム、エチレン酢酸ビニル共重合
体フイルム、エチレンビニルアルコール共重合体
フイルム、アイオノマー等のプラスチツクフイル
ム若しくはアルミニウム、銅、錫、鉄、鉛等の箔
等、又は以上の各基体の材料の適宜な複合体が使
用しうる。 First, the substrates include paper such as tissue paper, parchment paper, and kraft paper, polyethylene film, polypropylene film, polyvinyl chloride film, polyvinylidene chloride film, polyvinyl alcohol film, polyethylene terephthalate film, polycarbonate film, nylon film, polystyrene film, and ethylene film. A vinyl acetate copolymer film, an ethylene vinyl alcohol copolymer film, a plastic film such as an ionomer, a foil of aluminum, copper, tin, iron, lead, etc., or an appropriate composite of each of the above base materials may be used. sell.
次に剥離性層としては、適宜なベヒクルを主体
としてなるもの又は更にシリコーン若しくはワツ
クス等を添加してなる剥離性塗料を用いて公知の
塗布方法若しくは印刷方法により設けてなるもの
が例示される。剥離性塗料を構成するベヒクルと
してはエチルセルロース、エチルヒドロキシエチ
ルセルロース、セルロースアセテートプロピオネ
ート、酢酸セルロース等のセルロース誘導体、ポ
リスチレン、ポリαメチルスチレンなどのスチレ
ン樹脂及びスチレン共重合体樹脂、ポリメタクリ
ル酸メチル、ポリメタクリル酸エチル、ポリアク
リル酸エチル、ポリアクリル酸ブチルなどの、ア
クリル又はメタクリル樹脂の単独又は共重合樹
脂、ロジン、ロジン変性マレイン酸樹脂、ロジン
変性フエノール樹脂、重合ロジンなどのロジンエ
ステル樹脂、ポリ酢酸ビニル樹脂、クマロン樹
脂、ビニルトルエン樹脂、塩化ビニル樹脂、ポリ
エステル樹脂、ポリウレタン樹脂、ブチラール樹
脂、ポリアミド樹脂、塩化ビニル―酢酸ビニル共
重合樹脂等の1種又は2種以上を用い、以上のベ
ヒクルに可塑剤、安定剤、分散剤、体質顔料、溶
剤及び稀釈剤を適宜添加し、混練し、更にワツク
ス若しくはシリコーン等を添加して剥離性塗料と
し、又、以上のような剥離性塗料を用いて前記の
基体に剥離性層を設ける方法としては、グラビア
コート、ロールコート、エアーナイフコート、キ
スコート、スプレーコート、かけ流しコート、デ
イツプコート、スピンナーコート、ホイーラーコ
ート、刷毛塗り若しくはグラビア印刷、グラビア
オフセツト印刷、平版オフセツト印刷、ダイリソ
印刷、凸版印刷、凹版印刷、シルクスクリーン印
刷、静電印刷等の印刷方法によつて行なうことが
できる。 Next, examples of the releasable layer include those formed mainly of a suitable vehicle, or those formed by a known coating method or printing method using a releasable paint further containing silicone or wax. Vehicles constituting the peelable paint include cellulose derivatives such as ethyl cellulose, ethyl hydroxyethyl cellulose, cellulose acetate propionate, and cellulose acetate, polystyrene, styrene resins and styrene copolymer resins such as polyα-methylstyrene, polymethyl methacrylate, Single or copolymer resins of acrylic or methacrylic resins such as polyethyl methacrylate, polyethyl acrylate, polybutyl acrylate, rosin, rosin ester resins such as rosin-modified maleic acid resin, rosin-modified phenolic resin, polymerized rosin, poly Using one or more of vinyl acetate resin, coumaron resin, vinyl toluene resin, vinyl chloride resin, polyester resin, polyurethane resin, butyral resin, polyamide resin, vinyl chloride-vinyl acetate copolymer resin, etc., in the above vehicle. Plasticizers, stabilizers, dispersants, extender pigments, solvents, and diluents are appropriately added and kneaded, and further wax or silicone is added to make a releasable paint, or using the above releasable paint. Methods for providing a releasable layer on the substrate include gravure coating, roll coating, air knife coating, kiss coating, spray coating, continuous coating, dip coating, spinner coating, wheeler coating, brush coating or gravure printing, and gravure offset printing. This can be carried out by printing methods such as lithographic offset printing, dilithography, letterpress printing, intaglio printing, silk screen printing, and electrostatic printing.
或いは又、前記した基材にポリエチレン樹脂、
ポリプロピレン樹脂、エチレン―酢酸ビニル共重
合樹脂等の樹脂の溶融押出法によつて剥離性層を
設けてもよい。 Alternatively, polyethylene resin,
The peelable layer may be provided by melt extrusion of a resin such as polypropylene resin or ethylene-vinyl acetate copolymer resin.
以上のような剥離性層は基材と後述する加熱発
泡性模様及び通常の印刷層との接着性及び剥離性
を考慮して適宜選択して設けるが、剥離性層を設
けなくても基体表面が元来剥離性を有するもので
あれば剥離性層を設けなくてもよく、かかる基体
としてはポリエチレン、ポリプロピレン、ポリエ
ステル、ナイロン等のフイルム若しくはシートを
例示することができる。 The above-mentioned releasable layer is selected and provided as appropriate in consideration of the adhesion and releasability between the base material and the heat-foamable pattern and normal printing layer described below. If the substrate originally has releasability, it is not necessary to provide a releasable layer, and examples of such substrates include films or sheets of polyethylene, polypropylene, polyester, nylon, and the like.
以上のような基体の表面若しくは表面に剥離性
層を有する基体の剥離性層の表面に形成する加熱
発泡性模様としては、適宜なベヒクルを用いたイ
ンキに発泡剤を混入してなる加熱発泡性インキを
用い、公知の印刷方法によつて形成してなるもの
が挙げられる。 The heat-foamable pattern formed on the surface of a substrate or the surface of a peelable layer of a substrate having a peelable layer on the surface as described above is a heat-foamable pattern formed by mixing a foaming agent into an ink using an appropriate vehicle. Examples include those formed by a known printing method using ink.
発泡性インキを構成するベヒクルとしては、前
記した剥離性塗料を構成するベヒククルとして挙
げたものを使用することができ、更にこれらのベ
ヒクルに可塑剤、安定剤、分散剤、体質顔料、染
料・顔料の着色剤、溶剤及び希釈剤を適宜添加
し、更に発泡剤として重炭酸ナトリウム、炭酸ア
ンモニウム、ソジウムボロンハイドライド、シリ
コンオキシハイドライド等の無機発泡剤、アゾジ
カルボンアミド、アゾビスイソブチロニトリル、
ジニトロソペンタメチレンテトラミン、パラトル
エンスルホニルヒドラジツド、4,4′―オキシビ
スベンゼンスルホニルヒドラジツド等の有機発泡
剤、更には、気体や低沸点の有機溶剤を内包した
ミクロバルーン(又はミクロスフエアー)をベヒ
クル100重量部に対して1〜10好ましくは2〜8
重量部添加し混練して発泡性インキを作成し、以
上のような発泡性インキを用いて印刷する方法と
しては公知のグラビア印刷、グラビアオフセツト
印刷、平版オフセツト印刷、ダイリソ印刷、凸版
印刷、凹版印刷、ジエツトプリント、シルクスク
リーン印刷、静電印刷等の印刷方法を例示するこ
とができ、インキ転移量が比較的多いグラビア印
刷、シルクスクリーン印刷が好ましいが、本発明
においては発泡性模様が発泡する事により、該模
様部が突出するから、通常の印刷条件に比べて格
段に転移量を多くする必要はなく、グラビア印刷
においてはグラビア版の版深は100〜250μm、好
ましくは200〜220μmであり、シルクスクリーン
印刷においてはスクリーン線数は100〜20線/
inch、好ましくは40〜20線/inchである。 As the vehicle constituting the foamable ink, those listed above as the vehicle constituting the releasable paint can be used, and in addition to these vehicles, plasticizers, stabilizers, dispersants, extender pigments, dyes and pigments can be used. Colorants, solvents and diluents are added as appropriate, and inorganic blowing agents such as sodium bicarbonate, ammonium carbonate, sodium boron hydride, silicon oxyhydride, azodicarbonamide, azobisisobutyronitrile,
Organic blowing agents such as dinitrosopentamethylenetetramine, paratoluenesulfonylhydrazide, 4,4'-oxybisbenzenesulfonylhydrazide, etc., and microballoons (or microspheres) containing gas or low-boiling organic solvents, etc. ) to 100 parts by weight of vehicle, preferably 2 to 8
The foaming ink is prepared by adding parts by weight and kneading, and the methods of printing using the foaming ink as described above include known gravure printing, gravure offset printing, lithographic offset printing, dilithography, letterpress printing, and intaglio printing. Examples of printing methods include printing, jet printing, silk screen printing, electrostatic printing, etc., and gravure printing and silk screen printing, which have a relatively large amount of ink transfer, are preferred, but in the present invention, the foaming pattern is By doing so, the pattern part protrudes, so there is no need to increase the amount of transfer significantly compared to normal printing conditions, and in gravure printing, the plate depth of the gravure plate is 100 to 250 μm, preferably 200 to 220 μm. Yes, in silk screen printing, the number of screen lines is 100 to 20 lines/
inch, preferably 40 to 20 lines/inch.
次に発泡抑制模様について述べると、かかる発
泡抑制模様としては、発泡剤の分解を妨げるが若
しくは発泡剤の発泡を促進する発泡促進剤の働き
を妨げるような化合物を含む組成物を用いて形成
することができ、かかる化合物即ち発泡抑制剤と
しては日本特許第578566号(特公昭43―28636号
公報)に記載されているが、例えば、マレイン
酸、フマル酸、アジピン酸、1,2―フタル酸の
ような有機酸、特に少なくとも2個のカルボキシ
ル基及び1個の水酸基を含み炭素数が2〜12個の
有機酸:炭素数2〜20の有機酸ハライド、特に酸
塩化物:炭素数2〜20の有機酸無水物:2個の官
能基を有する炭素数が2〜20の多価芳香族アルコ
ール及びケトン:炭素数3〜12の飽和アミン又は
非飽和の6〜10員環アミン等から用途に合わせ、
例えば被転写材料の加熱発泡性基材に用いる発泡
剤、発泡助剤、安定剤との組合せにより発泡温度
を上昇する効果を有するものを選択して用い、適
宜なベヒクル、例えば前記した剥離性層を構成す
る剥離性塗料のベヒクルとして挙げたベヒクルの
うちから、被転写材料との接着性、耐熱性、用途
に合わせた物性を具備するものを選択し、以上の
ようなベヒクル及び前記した化合物に更に顔料若
しくは染料の着色剤、可塑剤、安定剤、分散剤、
体質顔料、溶剤及び希釈剤を適宜添加して混練し
てなる発泡抑制インキを用いて、公知の印刷方法
により設けてなるものを挙げることができる。 Next, regarding the foam suppression pattern, the foam suppression pattern is formed using a composition containing a compound that prevents the decomposition of the foaming agent or inhibits the action of the foaming promoter that promotes the foaming of the foaming agent. Such compounds, that is, foam suppressants, are described in Japanese Patent No. 578566 (Japanese Patent Publication No. 43-28636), and examples thereof include maleic acid, fumaric acid, adipic acid, and 1,2-phthalic acid. Organic acids, especially organic acids containing at least two carboxyl groups and one hydroxyl group and having 2 to 12 carbon atoms: Organic acid halides having 2 to 20 carbon atoms, especially acid chlorides: 2 to 2 carbon atoms 20 organic acid anhydrides: polyhydric aromatic alcohols with 2 to 20 carbon atoms and ketones having 2 functional groups: saturated amines with 3 to 12 carbon atoms or unsaturated 6- to 10-membered ring amines, etc. According to
For example, a foaming agent, a foaming aid, and a stabilizer used in the heat-foamable base material of the transfer material are selected and used in combination with a foaming agent that has the effect of increasing the foaming temperature, and an appropriate vehicle, such as the above-mentioned peelable layer, is used. From among the vehicles listed as vehicles for the releasable paint constituting the releasable paint, select one that has adhesion to the transfer material, heat resistance, and physical properties suited to the intended use. Furthermore, coloring agents for pigments or dyes, plasticizers, stabilizers, dispersants,
Examples include those produced by a known printing method using an anti-foaming ink prepared by adding and kneading extender pigments, solvents and diluents as appropriate.
本発明の転写紙には以上の他、通常のインキに
よる通常の模様を設けてもよく、又、通常の模
様、加熱発泡性模様及び発泡抑制模様は例えば、
同一の印刷機の各ユニツトを用いて設ける等の方
法により適宜同調整合して設けることができる。 In addition to the above, the transfer paper of the present invention may be provided with a normal pattern using normal ink, and the normal pattern, heat-foamable pattern, and foam-suppressing pattern may include, for example,
They can be provided by suitably adjusting and matching them by a method such as providing each unit of the same printing machine.
次に以上のような本発明の転写紙を用いた本発
明の化粧材の製造法について説明する。 Next, a method for manufacturing the decorative material of the present invention using the transfer paper of the present invention as described above will be explained.
まず本発明の転写紙の模様が設けられている面
と加熱発泡性素材とを接触させて前記素材に前記
加熱発泡性インキからなる加熱発泡性模様及び発
泡抑制インキからなる発泡抑制模様を転写する。
加熱発泡性素材としては、熱可塑性合成樹脂に発
泡剤を添加し、適宜な方法によりフイルム若しく
はシート化した未発泡のものが使用でき、熱可塑
性合成樹脂としては、例えばポリエチレン、ポリ
プロピレン等のポリオレフイン:エチレン―酢酸
ビニル共重合体、アイオノマー、エチレン―ビニ
ルアルコール共重合体等のポリオレフイン系共重
合体、ポリスチレン、ポリ塩化ビニル、ポリ酢酸
ビニル、塩化ビニル―酢酸ビニル共重合体、ナイ
ロン、アクリル等の合成樹脂を用い、発泡剤とし
ては、前記した加熱発泡性模様を構成する加熱発
泡性インキに用いるのと同様な発泡剤のうちか
ら、用いる合成樹脂の軟化点、発泡温度、若しく
は発泡抑制模様を構成する組成物に用いる発泡抑
制剤との組み合わせを考慮して選択し、更に、可
塑剤、安定剤、顔料若しくは染料の着色剤、発泡
促進剤、滑剤、帯電防止剤、紫外線吸収剤、等を
適宜混練してなる加熱発泡性樹脂組成物を用い、
例えば、公知の塗布方法、グラビアコート、ロー
ルコート、エアーナイフコート、キスコート、ス
プレーコート、かけ流しコート、デイツプコー
ト、スピンナーコート、ホイーラーコート、刷毛
塗り、シルクスクリーンによるベタコート、ワイ
ヤーバーコート等の方法により前記した転写紙の
印刷面に加熱発泡性樹脂組成物を塗布する方法に
よるか、又は適当な支持担体、例えばアスベスト
シート、紙、特にガラス繊維混抄紙、織布、特に
ガラス繊維織布、不織布、特にガラス繊維不織布
に塗布乾燥した後、該塗布面に前記転写紙の印刷
面を接触させて加熱及び加圧して転写する方法、
若しくは適宜な剥離性支持担体の表面に前記した
加熱発泡性樹脂組成物を塗布し、必要に応じて前
記した支持担体と複合し乾燥させて剥離性支持担
体を剥した後、剥離性支持担体を剥した後の表面
に転写紙を接触させて加熱及び加圧して転写する
方法等により、前記転写紙の模様が設けられてい
る面と加熱発泡性素材とを接触させて前記素材に
前記加熱発泡性模様及び発泡抑制模様を転写す
る。前記において加熱及び加圧して転写する際に
は、熱プレスを用いるか若しくは熱ロールを用い
て行なうとよく、転写の条件は転写紙及び加熱発
泡性素材によつて異なるが、熱プレスを用いると
きは熱板温度150℃〜200℃、圧力50〜70Kg/cm2、
熱ロールを用いるときは熱ロールの表面温度180
〜220℃、熱ロールと、転写紙及び加熱発泡性素
材を介して対向するロールとの間の線圧8〜10
Kg/cmである。 First, the patterned surface of the transfer paper of the present invention is brought into contact with a heat-foamable material to transfer the heat-foamable pattern made of the heat-foamable ink and the foam-suppressing pattern made of the foam-suppressing ink to the material. .
As the heat-foamable material, an unfoamed material made by adding a foaming agent to a thermoplastic synthetic resin and forming it into a film or sheet by an appropriate method can be used. Examples of the thermoplastic synthetic resin include polyolefins such as polyethylene and polypropylene: Synthesis of polyolefin copolymers such as ethylene-vinyl acetate copolymers, ionomers, ethylene-vinyl alcohol copolymers, polystyrene, polyvinyl chloride, polyvinyl acetate, vinyl chloride-vinyl acetate copolymers, nylon, acrylic, etc. A resin is used, and the foaming agent is selected from the same foaming agents as those used in the heat-foamable ink that forms the heat-foamable pattern described above, depending on the softening point, foaming temperature, or foaming temperature of the synthetic resin used, or the foaming agent that forms the foam-suppressing pattern. In addition, plasticizers, stabilizers, colorants such as pigments or dyes, foam accelerators, lubricants, antistatic agents, ultraviolet absorbers, etc. are selected as appropriate. Using a heat-foamable resin composition obtained by kneading,
For example, the above may be applied by a known coating method such as gravure coating, roll coating, air knife coating, kiss coating, spray coating, continuous coating, dip coating, spinner coating, wheeler coating, brush coating, solid coating by silk screen, wire bar coating, etc. A heat-foamable resin composition is applied to the printed surface of the transfer paper, or a suitable support carrier such as asbestos sheet, paper, especially glass fiber mixed paper, woven fabric, especially glass fiber woven fabric, non-woven fabric, especially A method of coating and drying a glass fiber nonwoven fabric, and then bringing the printed surface of the transfer paper into contact with the coated surface and applying heat and pressure to transfer;
Alternatively, the heat-foamable resin composition described above is applied to the surface of an appropriate releasable support carrier, and if necessary, it is composited with the above-described support carrier, dried, and the releasable support carrier is peeled off, and then the releasable support carrier is removed. The patterned surface of the transfer paper is brought into contact with the heat-foamable material by a method of transferring the transfer paper by contacting the peeled surface with heat and pressure. Transfer the texture pattern and the foaming suppression pattern. When transferring by applying heat and pressure in the above, it is best to use a heat press or a heat roll.The transfer conditions vary depending on the transfer paper and heat-foamable material, but when using a heat press, The heating plate temperature is 150℃~200℃, the pressure is 50~70Kg/ cm2 ,
When using a heat roll, the surface temperature of the heat roll is 180℃.
~220℃, linear pressure between the heated roll and the opposing roll through the transfer paper and heat-foamable material 8-10
Kg/cm.
以上のようにして加熱発泡性素材に加熱発泡性
模様及び発泡抑制模様を転写した後、必要に応じ
て製品となつた後化粧材の表面を保護する透明保
護層を設け、しかる後全体を加熱し加熱発泡性素
材を発泡させる。透明保護基を設けるには前記し
た加熱発泡性樹脂組成物において用いるのと同様
な合成樹脂を用い、可塑剤、安定剤、滑剤、帯電
防止剤、紫外線吸収剤等を適宜添加し混練してな
る透明樹脂組成物を用い、前記した加熱発泡性樹
脂組成物の塗布方法と同様の方法によつて設ける
ことができる。全体を加熱し加熱発泡性素材を発
泡させるには、熱風炉、遠赤外線ヒーター等の公
知の手段を用い、加熱の条件は、加熱発泡性素材
を構成する合成樹脂、可塑剤、発泡剤の組み合わ
せ、配合比によつても異なるが、180℃〜200℃、
所要時間は1〜3分である。 After transferring the heat-foamable pattern and the foam-suppressing pattern to the heat-foamable material as described above, a transparent protective layer is applied to protect the surface of the decorative material after it is made into a product, if necessary, and then the whole is heated. The heat-foamable material is foamed. To provide a transparent protective group, a synthetic resin similar to that used in the heat-foamable resin composition described above is used, and a plasticizer, stabilizer, lubricant, antistatic agent, ultraviolet absorber, etc. are appropriately added and kneaded. It can be provided using a transparent resin composition by a method similar to the method for applying the heat-foamable resin composition described above. In order to heat the entire material and foam the heat-foamable material, a known means such as a hot air stove or a far-infrared heater is used, and the heating conditions are a combination of the synthetic resin, plasticizer, and foaming agent that make up the heat-foamable material. , depending on the blending ratio, 180℃~200℃,
The required time is 1 to 3 minutes.
本発明は以上のような構成を有するので、本発
明の転写紙上に設けられた加熱発泡性模様は格別
固形分の多いインキを用いなくても形成でき、従
つてインキの粘弾性は印刷上好ましい範囲とする
ことが出来、しかも乾燥速度が遅い欠点もなく、
また加熱で自身が膨張する加熱発泡性インキの転
移量は通常の模様インキを使用する印刷条件に比
べて転移量を多くする必要もないから、加熱発泡
性模様は厚みを小さく形成でき、転写紙が枚葉印
刷方式によつて製造されて堆積されるとき又は輪
転方式によつて製造されて巻取られるときその印
刷模様がつぶれることがなく、剥離性基体が変形
して転写の際剥離しにくい等の欠点もなく、しか
も従来の発泡抑制剤のみを用いて転写紙に模様を
形成した場合に比較して、発泡抑制剤のみの多量
使用に起因する抑制イン印刷面のベトつきが少な
く通常の色インキを使用した多色印刷等の重ね印
刷もでき、巻取つた後にブロツキングが発生する
ことがないものである。 Since the present invention has the above configuration, the heat-foamable pattern provided on the transfer paper of the present invention can be formed without using an ink with a particularly high solid content, and therefore the viscoelasticity of the ink is favorable for printing. range, and there is no disadvantage of slow drying speed.
In addition, the transfer amount of heat-foamable ink, which expands when heated, does not need to be increased compared to printing conditions using normal pattern ink, so heat-foamable patterns can be formed with a small thickness, and transfer paper When it is manufactured by a sheet-fed printing method and deposited, or manufactured by a rotary printing method and wound up, the printed pattern is not crushed, and the releasable substrate is deformed and difficult to peel off during transfer. Moreover, compared to the case where a pattern is formed on transfer paper using only a conventional foaming inhibitor, there is less stickiness on the printed surface of the suppression ink due to the use of a large amount of foaming inhibitor only. It can also be used for overprinting such as multicolor printing using colored inks, and blocking does not occur after winding.
更に本発明の化粧材の製造法によれば、加熱に
より発泡膨張した加熱発泡性素材の表面よりさら
に突出した凸部と、該加熱発泡性素材の表面より
窪んだ凹部とを有する化粧材を一度の転写工程に
より設けることができ、しかも、得られる凸部は
加熱発泡性インキからなる加熱発泡性模様が転写
し発泡せられてなるものであるから加熱発泡性素
材が発泡してなるものと同様の柔軟性を与えるこ
とが出来、凸部を固形分の多いインキを用いて形
成した場合にくらべ凸部のみが摩耗する欠点がな
く、又、発泡抑制インキによる凹状模様に加え、
それ自身が加熱発泡する加熱発泡性インキによる
凸状模様が加熱発泡性素材の表面より突出して形
成されるため、発泡抑制剤の量の調節によつて凹
凸模様を形成する従来の方法に比べ、凹凸模様の
コントラストが大きく、より明瞭な模様を表わす
ことができ、空気中からの水分吸収等の経時変化
による抑制効果を低下させる性質を有する発泡抑
制剤のみを使用していないため、凹凸階調変化を
起しにくく、均一で安定した凹凸模様の化粧材を
製造できるという効果を有し、なお本発明の化粧
材の製造法は従来、転写紙を用いて行なわれてい
るいわゆるケキカルエンボス方式のクツシヨンフ
ロアー、壁紙等の製造ラインを用いて容易に実施
でき、得られるそれらのクツシヨンフロアー、壁
紙等の化粧材は繊細な興趣感に富む凸部及び凹部
を有する。 Furthermore, according to the method for producing a decorative material of the present invention, a decorative material having a convex portion further protruding from the surface of the heat-foamable material that has been foamed and expanded by heating, and a recessed portion recessed from the surface of the heat-foamable material is once produced. It can be provided by the transfer process of 1, and since the resulting convex portion is formed by transferring and foaming a heat-foamable pattern made of heat-foamable ink, it is similar to that formed by foaming a heat-foamable material. In addition to the concave pattern created by the anti-foaming ink, there is no disadvantage that only the convex portions are worn compared to when the convex portions are formed using ink with a high solid content.
The convex pattern created by the heat-foamable ink, which itself heat-foams, is formed so as to protrude from the surface of the heat-foamable material, so compared to the conventional method of forming a concavo-convex pattern by adjusting the amount of foaming inhibitor. The contrast of the uneven pattern is large, making it possible to express a clearer pattern, and because it does not use only a foaming inhibitor that has the property of reducing the suppressing effect due to changes over time such as moisture absorption from the air, the uneven gradation It has the effect of being able to produce a decorative material with a uniform and stable uneven pattern that does not easily change, and the method for producing the decorative material of the present invention is a method of manufacturing the so-called Kekikaru emboss method, which is conventionally carried out using transfer paper. It can be easily carried out using a production line for cushion floors, wallpaper, etc., and the resulting decorative materials such as cushion floors, wallpaper, etc. have delicate and interesting convex and concave portions.
以下に本発明をより具体的に示すための実施例
を掲げる。 Examples are given below to more specifically illustrate the present invention.
実施例
上質紙(坪量50g/m2)の表面にエクストル―
ジヨンコーテイング方式によりポリプロピレン樹
脂からなる剥離層を厚みが25μmになるように設
け、更に剥離層上に重ねて、塩ビ酢ビ共重合樹脂
系の塩ビ印刷用グラビアインキを用いてグラビア
印刷により模様を印刷し、しかる後、同様の塩ビ
印刷用インキに発泡抑制剤としてトリメリツト酸
無水物をベヒクル100重量部に対し80重量部添加
し混合してなる発泡抑制インキを用いて発泡抑制
模様を、模様を印刷するのと同様の塩ビ印刷用イ
ンキに発泡剤としてアゾジカルボンアミドをベヒ
クル100重量部に対し5重量部添加し混合してな
る発泡性インキを用いて発泡性模様をいずれもグ
ラビア印刷により印刷し、転写紙を作成した。Example: Extrude on the surface of high-quality paper (basis weight 50g/m 2 )
A release layer made of polypropylene resin is provided with a thickness of 25 μm using the Zion coating method, and a pattern is printed on the release layer using gravure printing using a vinyl chloride-vinyl acetate copolymer resin-based gravure ink for PVC printing. After that, a foam-suppressing pattern was printed using a foam-suppressing ink prepared by adding 80 parts by weight of trimellitic anhydride as a foaming inhibitor to 100 parts by weight of the vehicle to the same PVC printing ink. Using a foaming ink prepared by adding and mixing 5 parts by weight of azodicarbonamide as a foaming agent to 100 parts by weight of vehicle to a PVC printing ink similar to the above, foaming patterns were printed by gravure printing, I created a transfer paper.
一方、厚み0.7mmのアスベスト紙に下記組成の
加熱発泡性組成物をナイフコート法により、塗布
し温度160℃にて1分間加熱し乾燥させた後、表
面に前記の転写紙を印刷面が接触するようにして
重ね合わせ、表面温度200℃の加熱ロールを用い、
線圧8Kg/cm、速度0.1m/secで加熱及び加圧し
模様を転写した後、上質紙及び剥離層からなる剥
離紙を剥離した。 On the other hand, a heat-foamable composition with the following composition was applied to asbestos paper with a thickness of 0.7 mm by the knife coating method, heated at a temperature of 160°C for 1 minute and dried, and then the printed surface of the transfer paper was brought into contact with the surface. Layer them together in this way, and use a heating roll with a surface temperature of 200℃.
After transferring the pattern by heating and pressing at a linear pressure of 8 kg/cm and a speed of 0.1 m/sec, the release paper consisting of the high-quality paper and the release layer was peeled off.
加熱発泡性組成物
ポリ塩化ビニル樹脂 100重量部
(鐘淵化学工業製、カネカビニールペースト
PSL―37A)
ジオクチルフタレート 50 〃
エポキシ大豆油 2 〃
炭酸カルシウム 10 〃
TiO2 3 〃
ZnO 2 〃
アゾジカーボンアミド 3 〃
転写後、更に模様が転写された面に重ねて透明
塩ビプラスチゾルをワイヤーバーを用い、厚み
0.2mmになる様塗布し、その後、全体を温度200℃
で2分間加熱し発泡させたところ、発泡性模様の
部分が突出して凸部となり、発泡抑制模様の部分
が窪んで凹部となつた化粧材を得、得られた化粧
材は床材としてすぐれた外観を有し、かつ耐摩耗
性も良好であつた。Heat-foamable composition polyvinyl chloride resin 100 parts by weight (Kaneka Vinyl Paste, Kaneka Chemical Industry Co., Ltd.)
PSL-37A) Dioctyl phthalate 50 〃 Epoxy soybean oil 2 〃 Calcium carbonate 10 〃 TiO 2 3 〃 ZnO 2 〃 Azodicarbonamide 3 〃 After the transfer, overlay the pattern-transferred surface and apply transparent PVC plastisol with a wire bar. usage, thickness
Apply to a thickness of 0.2mm, then heat the entire surface to 200℃.
When heated for 2 minutes and foamed, a decorative material was obtained in which the foaming pattern part protruded and became a convex part, and the foaming suppressing pattern part became depressed and became a concave part, and the obtained decorative material was excellent as a flooring material. It had a good appearance and good wear resistance.
Claims (1)
が膨張する加熱発泡性インキからなる加熱発泡性
模様及び発泡抑制インキからなる発泡抑制模様を
形成してなることを特徴とする転写紙。 2 剥離性基体の剥離性を有する面に加熱で自身
が膨張する加熱発泡性インキからなる加熱発泡性
模様及び発泡抑制インキからなる発泡抑制模様を
形成してなる転写紙の加熱発泡性模様及び発泡抑
制模様が設けられている模様形成面と、加熱発泡
性素材とを接触させて該加熱発泡性素材に前記加
熱発泡性模様及び発泡抑制模様を転写し、しかる
後加熱発泡性素材を加熱発泡し、加熱発泡性模様
が転写された部分に発泡後の加熱発泡性素材表面
から突出する加熱発泡性インキによる凸状模様、
発泡抑制模様が転写された部分に発泡後の加熱発
泡性素材表面から窪んだ発泡抑制インキによる凹
状模様を形成させることを特徴とする化粧材の製
造法。[Scope of Claims] 1. A heat-foamable pattern made of a heat-foamable ink that expands when heated and a foam-suppressing pattern made of a foam-suppressing ink are formed on the releasable surface of a releasable substrate. transfer paper. 2 Heat-foamable pattern and foaming of transfer paper formed by forming a heat-foamable pattern made of a heat-foamable ink that expands by heating and a foam-suppressing pattern made of a foam-suppressing ink on the releasable surface of a releasable substrate The pattern forming surface provided with the suppression pattern is brought into contact with the heat-foamable material to transfer the heat-foamable pattern and the foam-suppression pattern to the heat-foamable material, and then the heat-foamable material is heated and foamed. , a convex pattern made of heat-foamable ink protruding from the surface of the heat-foamable material after foaming on the area to which the heat-foamable pattern has been transferred;
1. A method for producing a decorative material, which comprises forming a concave pattern made of foam suppressing ink, which is depressed from the surface of a heat-foamable material after foaming, on a portion to which a foam suppressing pattern has been transferred.
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56149050A JPS5851180A (en) | 1981-09-21 | 1981-09-21 | Transfer paper and method for producing decorative materials using the same |
| KR8203354A KR860000462B1 (en) | 1981-09-21 | 1982-07-27 | Method of manufacturing transfer paper and cosmetic material using the same |
| US06/419,525 US4482598A (en) | 1981-09-21 | 1982-09-17 | Transfer sheets and production of decorative articles therewith |
| EP82108688A EP0075832A1 (en) | 1981-09-21 | 1982-09-20 | Transfer sheets and production of decorative articles therewith |
| CA000411813A CA1197147A (en) | 1981-09-21 | 1982-09-21 | Transfer sheets and production of decorative articles therewith |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56149050A JPS5851180A (en) | 1981-09-21 | 1981-09-21 | Transfer paper and method for producing decorative materials using the same |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5851180A JPS5851180A (en) | 1983-03-25 |
| JPH0132791B2 true JPH0132791B2 (en) | 1989-07-10 |
Family
ID=15466550
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56149050A Granted JPS5851180A (en) | 1981-09-21 | 1981-09-21 | Transfer paper and method for producing decorative materials using the same |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5851180A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH10193538A (en) * | 1997-01-17 | 1998-07-28 | Dainippon Printing Co Ltd | Wall paper |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62124470U (en) * | 1986-01-30 | 1987-08-07 | ||
| JPH0729518B2 (en) * | 1987-03-12 | 1995-04-05 | 凸版印刷株式会社 | Transfer film |
| JPH0823206B2 (en) * | 1988-03-09 | 1996-03-06 | 株式会社アイジー技術研究所 | Hard wall material |
| JP7512715B2 (en) * | 2020-07-02 | 2024-07-09 | Toppanホールディングス株式会社 | Transfer sheet and decorative sheet using same |
| JP7574554B2 (en) * | 2020-07-02 | 2024-10-29 | Toppanホールディングス株式会社 | Transfer sheet and method for producing the same |
| JP2023163495A (en) * | 2022-04-28 | 2023-11-10 | 大日本印刷株式会社 | Decorative sheet laminate, decorative sheet, decorative transfer sheet, and decorative article |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS51139414A (en) * | 1975-05-26 | 1976-12-01 | Toppan Printing Co Ltd | Transfer sheet for producing decorating material with embossed surface |
| JPS5747018B2 (en) * | 1976-02-20 | 1982-10-06 |
-
1981
- 1981-09-21 JP JP56149050A patent/JPS5851180A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH10193538A (en) * | 1997-01-17 | 1998-07-28 | Dainippon Printing Co Ltd | Wall paper |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5851180A (en) | 1983-03-25 |
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