JP2002188273A - Protection method for floor members - Google Patents
Protection method for floor membersInfo
- Publication number
- JP2002188273A JP2002188273A JP2000387748A JP2000387748A JP2002188273A JP 2002188273 A JP2002188273 A JP 2002188273A JP 2000387748 A JP2000387748 A JP 2000387748A JP 2000387748 A JP2000387748 A JP 2000387748A JP 2002188273 A JP2002188273 A JP 2002188273A
- Authority
- JP
- Japan
- Prior art keywords
- ultraviolet
- film
- weight
- parts
- floor
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 238000000034 method Methods 0.000 title claims abstract description 19
- 239000000463 material Substances 0.000 claims description 45
- 238000000576 coating method Methods 0.000 claims description 21
- 239000011248 coating agent Substances 0.000 claims description 20
- 239000011342 resin composition Substances 0.000 claims description 18
- 229920002554 vinyl polymer Polymers 0.000 claims description 15
- 238000009408 flooring Methods 0.000 claims description 13
- 239000000203 mixture Substances 0.000 claims description 11
- 239000000178 monomer Substances 0.000 claims description 10
- 125000000129 anionic group Chemical group 0.000 claims description 7
- 238000010030 laminating Methods 0.000 claims description 6
- 239000003999 initiator Substances 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- 230000001678 irradiating effect Effects 0.000 claims description 2
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 2
- 229920005989 resin Polymers 0.000 abstract description 4
- 239000011347 resin Substances 0.000 abstract description 4
- 230000000704 physical effect Effects 0.000 abstract description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 17
- 239000001993 wax Substances 0.000 description 7
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- -1 tetrahydrofurfuryl Chemical group 0.000 description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 5
- 239000001301 oxygen Substances 0.000 description 5
- 229910052760 oxygen Inorganic materials 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 238000009472 formulation Methods 0.000 description 4
- 230000001681 protective effect Effects 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 230000005764 inhibitory process Effects 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
- 239000002904 solvent Substances 0.000 description 3
- 229920003002 synthetic resin Polymers 0.000 description 3
- 239000000057 synthetic resin Substances 0.000 description 3
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 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
- 239000004698 Polyethylene Substances 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical class C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000003475 lamination Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 2
- 229920000573 polyethylene Polymers 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
- 238000005406 washing Methods 0.000 description 2
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical group C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 1
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 1
- MSAHTMIQULFMRG-UHFFFAOYSA-N 1,2-diphenyl-2-propan-2-yloxyethanone Chemical compound C=1C=CC=CC=1C(OC(C)C)C(=O)C1=CC=CC=C1 MSAHTMIQULFMRG-UHFFFAOYSA-N 0.000 description 1
- 239000012956 1-hydroxycyclohexylphenyl-ketone Substances 0.000 description 1
- XMLYCEVDHLAQEL-UHFFFAOYSA-N 2-hydroxy-2-methyl-1-phenylpropan-1-one Chemical compound CC(C)(O)C(=O)C1=CC=CC=C1 XMLYCEVDHLAQEL-UHFFFAOYSA-N 0.000 description 1
- RZVJZTAYJDXIDT-UHFFFAOYSA-N 3-carbamoylbut-3-ene-1-sulfonic acid Chemical group NC(=O)C(=C)CCS(O)(=O)=O RZVJZTAYJDXIDT-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 101500000960 Bacillus anthracis Protective antigen PA-63 Proteins 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000007864 aqueous solution 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
- 230000005540 biological transmission Effects 0.000 description 1
- MQDJYUACMFCOFT-UHFFFAOYSA-N bis[2-(1-hydroxycyclohexyl)phenyl]methanone Chemical compound C=1C=CC=C(C(=O)C=2C(=CC=CC=2)C2(O)CCCCC2)C=1C1(O)CCCCC1 MQDJYUACMFCOFT-UHFFFAOYSA-N 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000012663 cationic photopolymerization Methods 0.000 description 1
- 229930016911 cinnamic acid Natural products 0.000 description 1
- 235000013985 cinnamic acid Nutrition 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 125000005678 ethenylene group Chemical group [H]C([*:1])=C([H])[*:2] 0.000 description 1
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 210000004907 gland Anatomy 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- 230000014759 maintenance of location Effects 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
- 238000005259 measurement Methods 0.000 description 1
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 239000012748 slip agent Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical group OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、床材の保護方法に
関するものである。The present invention relates to a method for protecting flooring.
【0002】[0002]
【従来の技術】現行の床材には、汚れを防ぎ、基材を保
護して、美観を保つために、被覆材をコーティングして
いるのが一般的である。2. Description of the Related Art Existing flooring materials are generally coated with a covering material in order to prevent dirt, protect a base material, and maintain aesthetic appearance.
【0003】このような被覆材としては、合成樹脂を溶
剤にて溶解させた溶剤タイプが一般的であったが、作業
環境、及び火気に対する危険性から、合成樹脂を水に分
散させたエマルジョンタイプ(特許第2597238号
公報)、紫外線硬化塗料を用いた紫外線硬化タイプ(特
開平6−279566号公報、特許第2549288号
公報)等が種々開発されている。[0003] As such a coating material, a solvent type in which a synthetic resin is dissolved in a solvent is generally used. However, an emulsion type in which the synthetic resin is dispersed in water is preferred due to the danger to the working environment and fire. (Japanese Patent No. 2597238), an ultraviolet-curable type using an ultraviolet-curable paint (JP-A-6-279566, Japanese Patent No. 2549288) and the like have been developed.
【0004】[0004]
【発明が解決しようとする課題】しかしながら、このよ
うな従来の床用被覆材において、エマルジョンタイプ
は、塗布後、完全硬化まで、1週間以上を要するという
問題が有り、また、紫外線硬化タイプは、酸素による硬
化阻害のため、表面物性が十分に発揮しにくいという問
題が有った。However, in such a conventional floor covering material, the emulsion type has a problem that it takes one week or more from application to complete curing, and the ultraviolet curing type has a problem. There is a problem that the surface properties are hardly sufficiently exhibited due to the inhibition of curing by oxygen.
【0005】酸素による硬化阻害を無くすために、光カ
チオン重合系が提案されてはいるが(特開平9−137
079号公報)、ラジカル重合と比較すれば硬化スピー
ドが遅いという問題が有った。In order to eliminate the inhibition of curing by oxygen, a cationic photopolymerization system has been proposed (JP-A-9-137).
No. 079), there is a problem that the curing speed is lower than that of radical polymerization.
【0006】また、いずれのタイプにおいても、ロー
ル、はけ塗り等で塗布するのが一般的であり、現場塗装
において、床材として使用可能な平滑性を出すには熟練
を要することも大きな問題の一つとなっている。[0006] Further, in any type, it is common to apply by a roll, brushing or the like, and it is also a great problem that in order to obtain smoothness usable as a floor material in on-site coating, skill is required. It has become one of.
【0007】さらに、補修及び意匠変更の簡便化のため
に、被覆材を除去出来るものが望まれており、除去性の
良好な被覆材も開発されている。(特許第254928
8号公報) 本発明は、このような点に鑑みてなされたものであり、
作業性が良好で、充分な表面物性と平滑性を持つ保護膜
が得られる床材の保護方法を提供することを目的とす
る。[0007] Further, for the purpose of simplifying repair and design change, a material capable of removing a coating material is desired, and a coating material having good removability has been developed. (Patent No. 254928
No. 8) The present invention has been made in view of such a point,
An object of the present invention is to provide a method for protecting a flooring material, which has good workability and can provide a protective film having sufficient surface physical properties and smoothness.
【0008】[0008]
【課題を解決するための手段】本発明の床材の保護方法
は、紫外線硬化性樹脂組成物が紫外線透過フィルムでラ
ミネートされてなる床用紫外線硬化型被覆材を、床材に
貼り付け、該フィルムの上から紫外線を照射して硬化さ
せて該床材と一体化させることを特徴とするものであ
る。According to the method for protecting a floor material of the present invention, an ultraviolet-curable coating material for a floor, in which an ultraviolet-curable resin composition is laminated with an ultraviolet-transmitting film, is attached to the floor material. It is characterized in that the film is irradiated with ultraviolet rays from above and cured to be integrated with the floor material.
【0009】この保護方法であると、被覆材として紫外
線硬化性樹脂組成物と紫外線透過フィルムとをラミネー
トしてなる紫外線硬化型被覆材を用いていることから、
作業性が良好である。また、表面にフィルムを付けたま
ま硬化させているので、酸素による硬化阻害を抑制して
充分な表面物性を持つとともに、平滑性に優れる保護膜
を形成することができる。According to this protection method, since an ultraviolet-curable coating material obtained by laminating an ultraviolet-curable resin composition and an ultraviolet-transmitting film is used as the coating material,
Workability is good. In addition, since the film is cured with the film attached to the surface, it is possible to form a protective film having sufficient surface properties by suppressing the curing inhibition by oxygen and having excellent smoothness.
【0010】本発明の床材の保護方法において、前記紫
外線硬化性樹脂組成物は下記(A)〜(D)よりなるこ
とが好ましい。In the method for protecting a flooring material of the present invention, the ultraviolet-curable resin composition preferably comprises the following (A) to (D).
【0011】 (A)紫外線硬化性モノマー 10〜90重量部 (B)ビニル重合体 10〜90重量部 (A)成分と(B)成分の合計100重量部に対し、 (C)光重合開始剤 1〜10重量部 (D)ワックス 0〜20重量部 このようにビニル重合体(B)を含む紫外線硬化性樹脂
組成物を用いることにより、被覆材を重ね塗りしたとき
の密着性が良好となり、補修が可能となる。(A) 10 to 90 parts by weight of an ultraviolet curable monomer (B) 10 to 90 parts by weight of a vinyl polymer (C) a photopolymerization initiator with respect to 100 parts by weight in total of the components (A) and (B) 1 to 10 parts by weight (D) wax 0 to 20 parts by weight By using the ultraviolet-curable resin composition containing the vinyl polymer (B) as described above, the adhesion when the coating material is repeatedly applied becomes good, Repair becomes possible.
【0012】また、このビニル重合体(B)として、陰
イオン性解離基を有するビニル重合体を用いる場合があ
り、その場合、被覆材に除去性を付与することができ、
被覆材の補修および意匠変更が簡便となる。Further, as the vinyl polymer (B), a vinyl polymer having an anionic dissociating group may be used, in which case the coating material can be provided with removability,
Repair of the covering material and design change are simplified.
【0013】[0013]
【発明の実施の形態】以下に本発明の実施に関連する事
項について詳細に説明する。DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS The matters relating to the implementation of the present invention will be described below in detail.
【0014】本発明における床用紫外線硬化型被覆材
は、紫外線硬化性樹脂組成物が紫外線透過フィルムでラ
ミネートされてなるものである。The ultraviolet ray-curable coating material for floors in the present invention is obtained by laminating an ultraviolet ray-curable resin composition with an ultraviolet ray transmitting film.
【0015】紫外線硬化性樹脂組成物としては、紫外線
硬化性モノマーと光重合開始剤とを含有し、紫外線によ
り硬化し得る樹脂組成物であれば、特に限定されない
が、好ましくは、紫外線硬化性モノマー(A)、ビニル
重合体(B)、光重合開始剤(C)、及びワックス
(D)からなる樹脂組成物を用いることである。The UV-curable resin composition is not particularly limited as long as it contains a UV-curable monomer and a photopolymerization initiator and can be cured by ultraviolet rays. (A), a vinyl polymer (B), a photopolymerization initiator (C), and a wax (D).
【0016】上記紫外線硬化性モノマー(A)として
は、公知慣用のものが使用可能であり、代表的なものと
しては、2−エチルヘキシルアクリレート、スチレン、
メチルメタクリレート、テトラヒドロフルフリル(メ
タ)アクリレート、フェノキシエチル(メタ)アクリレ
ート、イソボロニル(メタ)アクリレート、エチレング
リコールジ(メタ)アクリレート、プロピレングリコー
ルジ(メタ)アクリレート、ポリエチレングリコールジ
(メタ)アクリレート、ポリプロピレングリコールジ
(メタ)アクリレート、1,4ブタンジオールジ(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、EO変性ビスフェノールジ(メタ)アク
リレート、PO変性ビスフェノールジ(メタ)アクリレ
ート、トリメチロールプロパントリ(メタ)アクリレー
ト、EO変性トリメチロールプロパントリ(メタ)アク
リレート、PO変性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、トリス((メタ)アクリロキシエチル)
イソシアヌレート、ジペンタエリスリトールヘキサ(メ
タ)アクリレート、ジペンタエリスリトールペンタ(メ
タ)アクリレート、等が挙げられる。これらは単独で用
いても、複数種を併用しても構わない。As the UV-curable monomer (A), known and commonly used ones can be used. Typical examples thereof include 2-ethylhexyl acrylate, styrene,
Methyl methacrylate, tetrahydrofurfuryl (meth) acrylate, phenoxyethyl (meth) acrylate, isobornyl (meth) acrylate, ethylene glycol di (meth) acrylate, propylene glycol di (meth) acrylate, polyethylene glycol di (meth) acrylate, polypropylene glycol Di (meth) acrylate, 1,4 butanediol di (meth) acrylate, 1,6 hexanediol di (meth)
Acrylate, EO-modified bisphenol di (meth) acrylate, PO-modified bisphenol di (meth) acrylate, trimethylolpropane tri (meth) acrylate, EO-modified trimethylolpropane tri (meth) acrylate, PO-modified trimethylolpropane tri (meth) acrylate , Pentaerythritol tri (meta)
Acrylate, tris ((meth) acryloxyethyl)
Examples include isocyanurate, dipentaerythritol hexa (meth) acrylate, dipentaerythritol penta (meth) acrylate, and the like. These may be used alone or in combination of two or more.
【0017】上記ビニル重合体(B)としても公知のも
のが使用可能であり、単量体として典型的なビニル化合
物だけでなく、ビニリデン化合物やビニレン化合物など
の各種エチレン置換体を用いた重合体・共重合体を使用
することができる。単量体として、代表的なものとして
は、スチレン、エチルアクリレート、ブチルアクリレー
ト、メチルメタクリレート、2−エチルヘキシルアクリ
レート等が挙げられ、これらは単独で用いても、複数種
を併用しても構わない。As the vinyl polymer (B), known ones can be used. Polymers using not only typical vinyl compounds but also various ethylene-substituted monomers such as vinylidene compounds and vinylene compounds as monomers. -Copolymers can be used. Representative examples of the monomer include styrene, ethyl acrylate, butyl acrylate, methyl methacrylate, and 2-ethylhexyl acrylate. These may be used alone or in combination of two or more.
【0018】被覆材に除去性を付与するためには、ビニ
ル重合体(B)として陰イオン性解離基を有するものを
用いればよい。かかる陰イオン性解離基としては、カル
ボキシル基やスルホ基を挙げることができ、具体的に
は、単量体として、(メタ)アクリル酸、クロトン酸、
桂皮酸、マレイン酸(またはそのモノアルキルエステ
ル)、フマル酸(またはそのモノアルキルエステル)等
の重合性不飽和基含有カルボン酸、あるいは、ビニルス
ルホン酸、2−スルホエチルアクリルアミド等の重合性
不飽和基含有スルホン酸を用いて重合したビニル重合体
が挙げられる。これら単量体は単独で用いても、複数種
を併用しても構わない。また、これらの単量体ととも
に、陰イオン性解離基を有しない単量体を共重合成分と
して使用してもよく、このような共重合成分としては、
公知のものが使用可能であり、上記したスチレン、エチ
ルアクリレート、ブチルアクリレート、メチルメタクリ
レート、2−エチルヘキシルアクリレート等が挙げられ
る。In order to impart removability to the coating material, a vinyl polymer (B) having an anionic dissociating group may be used. Examples of such an anionic dissociating group include a carboxyl group and a sulfo group. Specifically, (meth) acrylic acid, crotonic acid,
Polymerizable unsaturated group-containing carboxylic acids such as cinnamic acid, maleic acid (or its monoalkyl ester) and fumaric acid (or its monoalkyl ester), or polymerizable unsaturated groups such as vinylsulfonic acid and 2-sulfoethylacrylamide. A vinyl polymer polymerized using a group-containing sulfonic acid is exemplified. These monomers may be used alone or in combination of two or more. In addition, together with these monomers, a monomer having no anionic dissociation group may be used as a copolymer component, such a copolymer component,
Known materials can be used, and examples thereof include styrene, ethyl acrylate, butyl acrylate, methyl methacrylate, and 2-ethylhexyl acrylate.
【0019】なお、ビニル重合体は公知の方法にて合成
でき、代表的なものとしては、溶液重合、乳化重合、懸
濁重合等が挙げられる。The vinyl polymer can be synthesized by a known method, and typical examples include solution polymerization, emulsion polymerization, suspension polymerization and the like.
【0020】光重合開始剤(C)としても公知のものが
使用可能で、代表的なものとしては、1−ヒドロキシシ
クロヘキシルフェニルケトン、2−ヒドロキシ−2−メ
チル−1−フェニルプロパン−1−オン、ベンジルジメ
チルケタール、ベンゾインイソプロピルエーテル、ベン
ゾフェノン等が挙げられる。これらは単独で用いても、
複数種を併用しても構わない。Known photopolymerization initiators (C) can be used, and typical examples thereof include 1-hydroxycyclohexylphenyl ketone and 2-hydroxy-2-methyl-1-phenylpropan-1-one. Benzyldimethyl ketal, benzoin isopropyl ether, benzophenone and the like. These can be used alone,
A plurality of types may be used in combination.
【0021】ワックス(D)としても公知のものが使用
可能であり、天然および合成の炭化水素ワックスやこれ
らの変性物、酸化物などの他、鉱物油および植物性油ワ
ックスやこれらの変性物などが挙げられる。ここで、ワ
ックス(D)は、融点が40℃以上のものが望ましい。
融点が40℃未満の場合、高温時に硬化皮膜のべとつき
が認められ、床用被覆材としての充分な機能を発揮しに
くい。Known waxes can also be used as the wax (D), such as natural and synthetic hydrocarbon waxes, modified products thereof, oxides, mineral oils and vegetable oil waxes and modified products thereof. Is mentioned. Here, the wax (D) desirably has a melting point of 40 ° C. or higher.
When the melting point is less than 40 ° C., the cured film becomes sticky at a high temperature, and it is difficult to exhibit a sufficient function as a floor covering material.
【0022】これら各成分の配合割合は、(A)成分1
0〜90重量部に対して(B)成分90〜10重量部で
ある。(B)成分が10重量部未満では、密着性や除去
性を高めるという(B)成分の効果が発揮されにくく、
また、90重量部を越えると、組成物の紫外線硬化性が
不十分となる場合がある。好ましくは、(A)成分が3
0〜70重量部で(B)成分が70〜30重量部であ
る。The mixing ratio of these components is as follows:
Component (B) is 90 to 10 parts by weight based on 0 to 90 parts by weight. When the amount of the component (B) is less than 10 parts by weight, the effect of the component (B) of enhancing the adhesion and the removability is hardly exhibited,
If the amount exceeds 90 parts by weight, the ultraviolet curability of the composition may be insufficient. Preferably, component (A) is 3
Component (B) is 70 to 30 parts by weight in 0 to 70 parts by weight.
【0023】上記(C)成分の配合割合は、(A)成分
と(B)成分の合計100重量部に対して1〜10重量
部であり、好ましくは2〜5重量部である。The proportion of the component (C) is 1 to 10 parts by weight, preferably 2 to 5 parts by weight, per 100 parts by weight of the total of the components (A) and (B).
【0024】上記(D)成分の配合割合は、(A)成分
と(B)成分の合計100重量部に対して0〜20重量
部である。この(D)成分は必須ではないが、添加する
ことにより、表面の光沢及び耐洗剤性が更に改善され
る。(D)成分の配合割合は、好ましくは0〜10重量
部である。The mixing ratio of the component (D) is 0 to 20 parts by weight based on 100 parts by weight of the total of the components (A) and (B). The component (D) is not essential, but by adding it, the gloss of the surface and the detergent resistance are further improved. The mixing ratio of the component (D) is preferably 0 to 10 parts by weight.
【0025】なお、この紫外線硬化性樹脂組成物には、
上記成分の他に必要に応じて、スリップ剤、界面活性
剤、可塑剤等の添加剤を添加しても良い。The UV-curable resin composition contains:
If necessary, additives such as a slip agent, a surfactant and a plasticizer may be added in addition to the above components.
【0026】また、(B)成分として、陰イオン性解離
基含有ビニル重合体を含む場合、紫外線硬化性樹脂組成
物は、酸価が30〜200mgKOH/gであることが好
ましい。30mgKOH/g未満では除去性に劣り、20
0mgKOH/gより大きければ耐水性に劣ることにな
る。When the component (B) contains an anionic dissociative group-containing vinyl polymer, the ultraviolet curable resin composition preferably has an acid value of 30 to 200 mgKOH / g. If it is less than 30 mgKOH / g, the removability is poor, and
If it is larger than 0 mgKOH / g, the water resistance will be poor.
【0027】本発明における床用紫外線硬化型被覆材
は、上記した紫外線硬化性樹脂組成物と紫外線透過フィ
ルムとをラミネートしてなるものである。すなわち、該
被覆材は、紫外線硬化性樹脂組成物を紫外線透過フィル
ム上に積層することにより、紫外線硬化性樹脂組成物か
らなる層と紫外線透過フィルムの層との少なくとも2層
からなるラミネート体として構成されている。The ultraviolet-curable floor covering material of the present invention is obtained by laminating the above-mentioned ultraviolet-curable resin composition and an ultraviolet-permeable film. That is, the coating material is formed as a laminate composed of at least two layers of a layer made of the ultraviolet-curable resin composition and a layer of the ultraviolet-permeable film by laminating the ultraviolet-curable resin composition on the ultraviolet-transparent film. Have been.
【0028】ラミネートに用いるフィルムは、紫外線を
透過するものであれば使用可能であり、例えば、ポリエ
チレン、ポリエチレンテレフタレート、ポリイミド等の
透明フィルムが挙げられる。Any film can be used as long as it transmits ultraviolet light, and examples of the film used for lamination include transparent films of polyethylene, polyethylene terephthalate, polyimide and the like.
【0029】ラミネートの仕方としては、フィルムの片
側に所定の膜厚になるように上記組成物をコーティング
したり、あるいはまた、上記組成物を2枚のフィルムの
間に所定の膜厚になるように挟んだりする方法が挙げら
れる。2枚のフィルムで挟む場合、2枚とも紫外線透過
フィルムとしてもよいが、1枚が紫外線透過フィルムで
あれば、もう1枚は剥離紙などの紫外線が透過しないフ
ィルムでもよい。As a method of laminating, one side of the film is coated with the above composition so as to have a predetermined thickness, or alternatively, the above composition is coated so as to have a predetermined thickness between two films. Or a method of sandwiching them. When sandwiched between two films, both may be ultraviolet-transmitting films, but if one is an ultraviolet-transmitting film, the other may be a film that does not transmit ultraviolet light, such as release paper.
【0030】以上よりなる床用紫外線硬化型被覆材を用
いて床材に保護膜を形成するためには、該被覆材を床材
表面の所望位置に貼り付け、紫外線透過フィルムを付け
たままの状態で紫外線を照射して樹脂組成物を硬化さ
せ、これにより床材と一体化させた後、表面のフィルム
を剥離すればよい。In order to form a protective film on a flooring material using the ultraviolet curing type coating material for floors constructed as described above, the coating material is attached to a desired position on the surface of the flooring material, and the ultraviolet light transmitting film is kept attached. The resin composition may be cured by irradiating the resin composition with ultraviolet rays in this state, thereby integrating the resin composition with the floor material, and then removing the film on the surface.
【0031】詳細には、2枚のフィルムでラミネートさ
れた場合は片方のフィルムを剥がしながら床材に貼り付
け、1枚のフィルムでラミネートされた場合はそのまま
床材に貼り付けて、フィルム(紫外線透過フィルム)の
上から高圧水銀ランプなどの紫外線照射装置で紫外線を
照射して硬化させる。このように、フィルムを付けたま
ま硬化させることができるため、基材表面に形成される
皮膜(保護膜)に平滑性を付与することができるととも
に、紫外線硬化樹脂の酸素による硬化阻害を防止するこ
とができる。More specifically, when two films are laminated, one film is peeled off and attached to a floor material, and when one film is laminated, the film is directly adhered to the floor material and the film (ultraviolet rays) UV light is irradiated from above the transmission film) with an ultraviolet irradiation device such as a high-pressure mercury lamp to cure the film. As described above, since the film can be cured with the film attached, the film (protective film) formed on the base material surface can be provided with smoothness, and the curing of the ultraviolet-curable resin is prevented from being inhibited by oxygen. be able to.
【0032】本発明における床材は、特に限定されるも
のではないが、代表的なものとしては、塩化ビニル樹
脂、ポリエステル樹脂、ポリウレタン樹脂、エポキシ樹
脂、アクリル樹脂、ポリオレフィン樹脂等の合成樹脂、
木材、石材等の天然素材が挙げられる。The floor material in the present invention is not particularly limited, but typical examples thereof include synthetic resins such as vinyl chloride resin, polyester resin, polyurethane resin, epoxy resin, acrylic resin, polyolefin resin, and the like.
Examples include natural materials such as wood and stone.
【0033】[0033]
【実施例】以下に本発明を実施例及び比較例により具体
的に説明するが、本発明はこれらの実施例により何ら限
定されるものではない。なお、以下において「部」及び
「%」は、特に断りのない限り、全て重量基準であるも
のとする。EXAMPLES The present invention will be specifically described below with reference to examples and comparative examples, but the present invention is not limited to these examples. In the following, “parts” and “%” are all based on weight unless otherwise specified.
【0034】下記表1に示す配合にて、配合1〜6の紫
外線硬化性樹脂組成物を調製した。The UV curable resin compositions of Formulations 1 to 6 were prepared according to the formulations shown in Table 1 below.
【0035】[0035]
【表1】 [Table 1]
【0036】実施例1〜5および比較例1については、
それぞれ下記表2に示す各配合の組成物を用いて、2枚
の透明なポリエチレンフィルムに厚み30μmになるよ
うに挟んでラミネート品の被覆材を作成した。そして、
塩ビ床材に、ラミネートされた被覆材の片方のフィルム
をはがしながら貼り付け、そのまま80W/cmの高圧
水銀ランプを用いて、積算照度350mJ/cm2の条
件で硬化させ、硬化後、表面のフィルムを剥離して、下
記の試験に供した。For Examples 1 to 5 and Comparative Example 1,
Using the compositions of the respective formulations shown in Table 2 below, a coating material for a laminated product was prepared by sandwiching two transparent polyethylene films so as to have a thickness of 30 μm. And
One film of the laminated coating material is attached to a PVC flooring material while peeling it off, and cured using an 80 W / cm high-pressure mercury lamp under the condition of an integrated illuminance of 350 mJ / cm 2 , and after curing, the surface film is cured. Was peeled off and subjected to the following test.
【0037】また、比較例2として、上記配合2を酢酸
エチルにて溶解させた溶剤系の被覆材を用いて、これを
塩ビ床材上に厚さ50μmで塗布し、80℃で30分間
乾燥してから高圧水銀ランプで硬化させた後、同様の試
験に供した。さらに、比較例3として、市販のウレタン
系フロアーポリッシュであるポリーズユシロンコートC
グランド(ユシロ化学社製)を用いて、これを塩ビ床材
上に3回塗布して、24時間以上放置してから同様の試
験に供した。As Comparative Example 2, a solvent-based coating material obtained by dissolving Formulation 2 in ethyl acetate was applied to a thickness of 50 μm on a PVC flooring material, and dried at 80 ° C. for 30 minutes. Then, after curing with a high-pressure mercury lamp, the same test was performed. Further, as Comparative Example 3, a commercially available urethane floor polish, POLYSUILON COAT C
Using a gland (manufactured by Yushiro Chemical Co., Ltd.), this was applied three times on a PVC flooring material, left for 24 hours or more, and subjected to the same test.
【0038】得られた皮膜についての試験項目及び条件
は、以下の通りである。The test items and conditions for the obtained film are as follows.
【0039】表面状態:硬化皮膜の表面状態を目視及び
指触にて評価した。Surface condition: The surface condition of the cured film was evaluated visually and by finger touch.
【0040】光沢度:JIS K 3920−14に準じ
て鏡面光沢度計にて光沢度(%)を測定した。Gloss: Gloss (%) was measured with a specular gloss meter according to JIS K 3920-14.
【0041】耐水性:JIS K 3920−17に準じ
て表面の白化状態を目視にて評価した。○は、変化が認
められなかったことを示す。Water resistance: The whitening state of the surface was visually evaluated according to JIS K 3920-17. ○ indicates that no change was observed.
【0042】除去性:5%KOH水溶液に硬化皮膜を3
0分間浸漬した後、流水にて充分にすすぎ、皮膜の状態
を目視にて評価した。○は除去性良好、×は除去性不良
を示す。Removability: 3 cured films in 5% KOH aqueous solution
After immersion for 0 minutes, the film was sufficiently rinsed with running water, and the state of the film was visually evaluated. ○ indicates good removability, and X indicates poor removability.
【0043】密着性:得られた各皮膜上に、それぞれ皮
膜と同一の被覆材を、同様の方法により積層形成した。
積層後の皮膜について、JIS K 5400−8.5
(碁盤目テープ法)に準じて測定し、100個のますめ
(1mm間隔)のうち、残った個数にて評価した。Adhesion: The same coating material as the coating was laminated on each of the obtained coatings in the same manner.
Regarding the film after lamination, JIS K 5400-8.5
The measurement was carried out according to the (cross-cut tape method), and the evaluation was made based on the number of remaining pieces out of 100 pieces (1 mm intervals).
【0044】耐洗剤性:JIS K 3920−18に準
じて洗浄前後の光沢度を測定し、光沢保持率にて評価を
行なった。Detergent resistance: The glossiness before and after washing was measured according to JIS K 3920-18, and the gloss retention was evaluated.
【0045】耐ヒールマーク性:JIS K 3920−
15に準じてヒールマークの付着度合いを目視で評価し
た。付着がほとんどないものを○、付着の著しいものを
×とした。Heel mark resistance: JIS K 3920-
According to No. 15, the degree of adhesion of the heel mark was visually evaluated.ほ と ん ど indicates that there was little adhesion, and X indicates that adhesion was significant.
【0046】[0046]
【表2】 結果は、表2に示す通りである。[Table 2] The results are as shown in Table 2.
【0047】実施例1〜5によれば、エマルジョンタイ
プの比較例3が24時間以上の養生が必要なのに比較し
て短時間で硬化し、また、紫外線硬化樹脂の特徴の一つ
である光沢度が高かった。しかも、フィルムを付けたま
ま硬化させているため、比較例2に比べて、皮膜表面の
平滑性に優れ、また、酸素による硬化阻害を受けずに良
好な表面物性を示した。According to Examples 1 to 5, the comparative example 3 of the emulsion type cures in a shorter time than the curing time of 24 hours or more is required, and the glossiness which is one of the characteristics of the ultraviolet curable resin. Was high. In addition, since the film was cured with the film attached, the film surface was excellent in smoothness as compared with Comparative Example 2, and showed good surface properties without being inhibited from curing by oxygen.
【0048】また、組成物中にビニル重合体を含有する
ため、重ね塗り時の密着性が良好であり、更に、組成物
中に陰イオン性解離基含有ビニル重合体を含む実施例1
〜3では、除去性にも優れていた。Further, since the composition contains a vinyl polymer, the adhesion at the time of recoating is good, and the composition contains a vinyl polymer containing an anionic dissociating group.
In Nos. To 3, the removability was excellent.
【0049】[0049]
【発明の効果】以上のように、本発明の床材の保護方法
は、作業環境を損なうことなく、かつ簡便で効率の良い
方法であるために、被覆作業の効率化を図ることができ
る。また、得られた皮膜も光沢、耐水、耐洗浄性等の表
面物性に優れる。As described above, the method for protecting flooring according to the present invention is a simple and efficient method without impairing the working environment, so that the efficiency of the covering operation can be improved. Further, the obtained film has excellent surface properties such as gloss, water resistance, and washing resistance.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) E04F 15/10 104 E04F 15/10 104A (72)発明者 斎藤 友尚 神奈川県高座郡寒川町田端1580番地 ユシ ロ化学工業株式会社内 (72)発明者 祝迫 浩一 滋賀県大津市本宮2丁目5−10−711 (72)発明者 菅原 輝明 滋賀県守山市石田町910−60 Fターム(参考) 4J011 AA05 PA56 PA63 PA69 PA70 PB40 QA03 QA09 QA12 QA13 QA23 QA24 QA25 QA33 QA37 QB16 RA03 RA04 RA10 RA11 SA01 SA21 SA31 SA51 UA01 WA02 ──────────────────────────────────────────────────の Continued on the front page (51) Int.Cl. 7 Identification symbol FI Theme coat ゛ (Reference) E04F 15/10 104 E04F 15/10 104A (72) Inventor Tomohisa Saito 1580 Tabata, Samukawa-cho, Koza-gun, Kanagawa Prefecture Yushiro Chemical Industry Co., Ltd. (72) Inventor Koichi Sakusako 2-5-10-711 Motomiya, Otsu City, Shiga Prefecture (72) Inventor Teruaki Sugawara 910-60 Ishidacho, Moriyama City, Shiga Prefecture F-term (reference) 4J011 AA05 PA56 PA63 PA69 PA70 PB40 QA03 QA09 QA12 QA13 QA23 QA24 QA25 QA33 QA37 QB16 RA03 RA04 RA10 RA11 SA01 SA21 SA31 SA51 UA01 WA02
Claims (5)
ルムでラミネートされてなる床用紫外線硬化型被覆材
を、床材に貼り付け、該フィルムの上から紫外線を照射
して硬化させて該床材と一体化させることを特徴とする
床材の保護方法。An ultraviolet-curable coating material for a floor, which is formed by laminating an ultraviolet-curable resin composition with an ultraviolet-transmissive film, is adhered to a floor material, and cured by irradiating ultraviolet rays from above the film. A method for protecting flooring, characterized by being integrated with the flooring.
(A)〜(D)よりなることを特徴とする請求項1記載
の床材の保護方法。 (A)紫外線硬化性モノマー 10〜90重量部 (B)ビニル重合体 10〜90重量部 (A)成分と(B)成分の合計100重量部に対し、 (C)光重合開始剤 1〜10重量部 (D)ワックス 0〜20重量部2. The method according to claim 1, wherein the ultraviolet curable resin composition comprises the following (A) to (D). (A) 10 to 90 parts by weight of an ultraviolet curable monomer (B) 10 to 90 parts by weight of a vinyl polymer (C) Photopolymerization initiator 1 to 10 based on a total of 100 parts by weight of the components (A) and (B) Parts by weight (D) wax 0 to 20 parts by weight
するビニル重合体であることを特徴とする請求項2記載
の床材の保護方法。3. The method according to claim 2, wherein the component (B) is a vinyl polymer having an anionic dissociating group.
〜200mgKOH/gであることを特徴とする請求項3
記載の床材の保護方法。4. An ultraviolet curable resin composition having an acid value of 30.
4. The composition according to claim 3, wherein the amount is from 200 mgKOH / g.
The method of protecting the flooring described.
はスルホ基を有するビニル重合体であることを特徴とす
る請求項3又は4記載の床材の保護方法。5. The method according to claim 3, wherein the component (B) is a vinyl polymer having a carboxyl group or a sulfo group.
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JP2000387748A JP2002188273A (en) | 2000-12-20 | 2000-12-20 | Protection method for floor members |
Applications Claiming Priority (1)
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JP2000387748A JP2002188273A (en) | 2000-12-20 | 2000-12-20 | Protection method for floor members |
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JP2000387748A Pending JP2002188273A (en) | 2000-12-20 | 2000-12-20 | Protection method for floor members |
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