JP2002225201A - Expanded decorative material - Google Patents
Expanded decorative materialInfo
- Publication number
- JP2002225201A JP2002225201A JP2001027795A JP2001027795A JP2002225201A JP 2002225201 A JP2002225201 A JP 2002225201A JP 2001027795 A JP2001027795 A JP 2001027795A JP 2001027795 A JP2001027795 A JP 2001027795A JP 2002225201 A JP2002225201 A JP 2002225201A
- Authority
- JP
- Japan
- Prior art keywords
- layer
- decorative material
- composite film
- foam
- ionomer
- 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.)
- Granted
Links
Landscapes
- Floor Finish (AREA)
- Laminated Bodies (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は床材壁材等の内装材
に適する塩素を含有しない発泡装飾材に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a chlorine-free foam decorative material suitable for interior materials such as floor materials and wall materials.
【0002】[0002]
【従来の技術】特開平9−59880号公報の非ハロゲ
ン床材には、上層が単に単層のアイオノマーである構成
が開示されている。この構成では、積層力が低く、白化
が起こった。さらに高価な上、シートの剛性が高く施工
しづらかった。2. Description of the Related Art Japanese Unexamined Patent Publication No. 9-59880 discloses a non-halogen floor material in which the upper layer is simply a single-layer ionomer. In this configuration, the lamination force was low, and whitening occurred. Further, the sheet was expensive and the rigidity of the sheet was high, making it difficult to construct.
【0003】特開平10−280284号公報は、非塩
ビ床材であって上層と、上層よりも柔らかい下層を有す
る複合フィルムが非塩ビ発泡層状に形成された床材が開
示されている。しかし上記床材はシワ、反り、耐傷性、
白化、施工性に問題があった。Japanese Patent Application Laid-Open No. 10-280284 discloses a non-PVC flooring material in which a composite film having an upper layer and a lower layer softer than the upper layer is formed in a non-PVC foam layer. However, the above flooring is wrinkled, warped, scratch resistant,
There were problems with whitening and workability.
【0004】[0004]
【発明が解決しようとする課題】本発明は、塩素を含有
しない床材等の発泡装飾材であって、耐傷性等の耐久性
の高い装飾材を提供する。SUMMARY OF THE INVENTION The present invention provides a foamed decorative material such as a flooring material containing no chlorine and having high durability such as scratch resistance.
【0005】[0005]
【課題を解決するための手段】本発明は塩素を含有しな
い樹脂発泡層上に、アイオノマーの上層と、該上層より
も柔らかい塩素を含有しないフィルムの下層からなる複
合フィルムが積層されたことを特徴とする発泡装飾材、
をその要旨とする。The present invention is characterized in that a composite film comprising an ionomer upper layer and a chlorine-free film lower than the upper layer is laminated on a chlorine-free resin foam layer. And foam decorative material,
Is the gist.
【0006】本発明において、発泡層上に上層と下層か
らなる複合フィルムが積層される。積層フィルムは2層
でも3層でもよい。上層はアイオノマーであり、マイナ
スイオン官能基を有する極性ポリマーが、Zn、Li、
Mg、Na等の金属イオンで架橋結合された構成であ
る。 アイオノマーとしては、MFRが1乃至15g/
10minであるのが望ましい。硬さとしてはシェアD
硬度50以上が望ましい。厚さは20μm以上、更に好
ましくは30〜200μm以上が望ましい。得られた複
合フィルムのアイオノマー部分は、結晶性と非晶性が相
混じっており、柔軟で白化しない。アイオノマーはハイ
ミラン(三井デュポンポリケミカル社製)として、市販
されており、包装用として使用される。この樹脂を表層
フィルムとして好適に利用される。得られた複合フィル
ムは、非塩ビ発泡体に積層される。In the present invention, a composite film comprising an upper layer and a lower layer is laminated on a foam layer. The laminated film may have two layers or three layers. The upper layer is an ionomer, and the polar polymer having a negative ion functional group is Zn, Li,
It is a structure cross-linked by metal ions such as Mg and Na. As an ionomer, the MFR is 1 to 15 g /
Desirably, it is 10 min. Share D as hardness
Hardness of 50 or more is desirable. The thickness is preferably at least 20 μm, more preferably at least 30 to 200 μm. The ionomer portion of the obtained composite film is a mixture of crystallinity and amorphousness, and is soft and does not whiten. The ionomer is commercially available as Himilan (manufactured by Du Pont-Mitsui Polychemicals) and is used for packaging. This resin is suitably used as a surface film. The obtained composite film is laminated on a non-PVC foam.
【0007】下層はアイオノマーより柔らかいフィルム
である。フィルムとしては、上層より柔らかいアイオノ
マー、EVA、ナイロン、アクリル系フィルム、ポリオ
レフィンが例示される。下層のMFRは0.1〜20g
/10minが好適である。The lower layer is a film that is softer than the ionomer. Examples of the film include an ionomer softer than the upper layer, EVA, nylon, an acrylic film, and a polyolefin. MFR of lower layer is 0.1-20g
/ 10 min is preferred.
【0008】上記上層と下層が積層された複合フィルム
が得られる。これらのフィルムは、厚さ20〜300μ
mが好適である。 本願発明において、上記複合フィル
ムは下層の表面側に上層が積層された構成で、この複合
フィルムの全厚は50〜500μmで上層:下層の厚み
の比が1:20〜20:1が望ましい。上記のような構
成の複合フィルムは、爪による傷つきがなく、耐傷性、
耐摩耗性が高い。下層フィルムは上層フィルムよりも柔
らかいので、発泡層との接着性が良い。[0008] A composite film in which the upper layer and the lower layer are laminated is obtained. These films have a thickness of 20-300μ.
m is preferred. In the present invention, the composite film has a configuration in which an upper layer is laminated on the surface side of a lower layer, and the total thickness of the composite film is preferably 50 to 500 μm, and the ratio of the thickness of the upper layer to the lower layer is preferably 1:20 to 20: 1. The composite film having the above configuration is free from scratches by nails,
High wear resistance. Since the lower film is softer than the upper film, it has good adhesion to the foam layer.
【0009】[0009]
【発明の実施の形態】「図1」は本発明発泡装飾材断面
図である。1は上層、2は下層、3は複合フィルムであ
り、4 は印刷層であり、5は発泡層である。印刷層直
下に寸法安定性付与のため、不織布、ネット等の繊維層
6を介在させても良い。FIG. 1 is a sectional view of a foam decorative material according to the present invention. 1 is an upper layer, 2 is a lower layer, 3 is a composite film, 4 is a printing layer, and 5 is a foam layer. A fiber layer 6 such as a nonwoven fabric or a net may be interposed immediately below the printing layer to provide dimensional stability.
【0010】不燃紙、塩素原子を含まない合成樹脂シー
ト、ガラス繊維の織布または不織布基材上1に成分中に
塩素原子を含まない樹脂、例えばエチレン−酢ビコポリ
マー(EVA)、エチレン−エチルアクリレート共重合
体、ポリアクリル酸エステル、ポリメタクリル酸エステ
ル、ポリオレフィン等の発泡性樹脂を押出機から0.2
〜1.0mm厚で塗布し、その上に繊維層6を積層し、
プレヒートオーブンにてプレヒートを行い、転写ロール
で樹脂層表面に転写により模様形成し、メインオーブン
にて120〜250℃で加熱発泡を行う。発泡倍率は
1.3〜20倍である。このように本発明発泡装飾材7
が得られる。On a non-combustible paper, a chlorine-free synthetic resin sheet, a glass fiber woven or non-woven fabric substrate 1, a resin containing no chlorine atoms in the components, for example, ethylene-vinyl acetate copolymer (EVA), ethylene-ethyl An acrylate copolymer, a polyacrylate, a polymethacrylate, a foamable resin such as a polyolefin is extruded from an extruder into a mold.
1.01.0 mm thick, and a fiber layer 6 is laminated thereon,
Preheating is performed in a preheat oven, a pattern is formed on the resin layer surface by transfer with a transfer roll, and heating and foaming are performed in a main oven at 120 to 250 ° C. The expansion ratio is 1.3 to 20 times. Thus, the foam decorative material 7 of the present invention
Is obtained.
【0011】また、とくにメタロセン触媒で重合された
ポリオレフィン(主としてPE)も好適である。一般的
なメタロセン触媒はメタロセン錯体とアルミノキサンに
よって構成される。このメタロセン触媒によるPEは、
シャープな分子量分布および組成分布を持ち、卓越した
低温ヒートシール性を有する。Polyolefins (mainly PE) polymerized with a metallocene catalyst are also suitable. A general metallocene catalyst is composed of a metallocene complex and an aluminoxane. This metallocene-catalyzed PE is
It has a sharp molecular weight distribution and composition distribution, and has excellent low-temperature heat sealability.
【0012】発泡剤としてはジニトロソペンタメチレン
テトラミン、ベンゼンスルホニルヒドラジド、p−トル
エンスルホニルヒドラジド、p、p’−オキシビス(ベ
ンゼンスルホニルヒドラジド)、3、3’−ジスルホン
ヒドラジドフェニルスルホン、アゾビスイソブチルニト
リル、アゾジカルボンアミド等が例示され、発泡促進剤
として尿素エタノールアミン、亜鉛華、炭酸鉛、ステア
リン酸鉛、ステアリン酸亜鉛、グリコール等が例示され
る。さらに充填剤として水酸化アルミニウム、重質炭酸
カルシウム、軽質炭酸カルシウム、クレー、タルク等が
例示される。Examples of the blowing agent include dinitrosopentamethylenetetramine, benzenesulfonylhydrazide, p-toluenesulfonylhydrazide, p, p'-oxybis (benzenesulfonylhydrazide), 3,3'-disulfonehydrazidephenylsulfone, azobisisobutylnitrile, Examples include azodicarbonamide and the like, and examples of the foaming accelerator include urea ethanolamine, zinc white, lead carbonate, lead stearate, zinc stearate, and glycol. Examples of the filler include aluminum hydroxide, heavy calcium carbonate, light calcium carbonate, clay, and talc.
【0013】発泡層をEVAとする時、発泡性樹脂の成
分構成は、EVA100PHRに対し、発泡剤1〜10
PHR、発泡促進剤0.1〜5PHR、顔料1〜20P
HR、充填剤0〜100 PHRが好ましい。このよう
にして得られた床材は燃焼時に有毒ガスを発生させず、
強度面でもPVCを用いた床材と比較して遜色がない
等、有用なものであった。When the foamed layer is made of EVA, the composition of the foamable resin is as follows: EVA100PHR, foaming agent 1 to 10
PHR, foaming accelerator 0.1-5PHR, pigment 1-20P
HR, fillers 0 to 100 PHR are preferred. The flooring material obtained in this way does not generate toxic gas during combustion,
In terms of strength, it was useful as compared with a floor material using PVC.
【0014】上記製造工程にて、押出機を用いて基材上
に塗布される発泡性樹脂に含有されている塩素原子を含
まない樹脂として好ましいのはEVA(MFRが0.1
〜20g/100min・好ましくは、MFRが1.0
〜10g/10min)、酢酸ビニル(VAc量5−4
0wt%)である。 なお、MFRは樹脂の流動性を示
す値であって、数字の大きい程流動性が高いことを示
す。(ASTM D−1238改)In the above production process, the resin containing no chlorine atom, which is contained in the foamable resin applied to the substrate by using an extruder, is preferably EVA (MFR of 0.1 or less).
~ 20 g / 10 0 min. Preferably, MFR is 1.0
-10 g / 10 min), vinyl acetate (VAc amount 5-4)
0 wt%). The MFR is a value indicating the fluidity of the resin, and the larger the number, the higher the fluidity. (ASTM D-1238 revised)
【0015】また発泡樹脂層をオーブンで加熱発泡直前
に複合フィルムを積層し、加熱発泡後エンボスロールで
加圧エンボスをして本願発泡装飾材の床材を得る。Further, the foamed resin layer is laminated with a composite film immediately before heating and foaming in an oven, and after heating and foaming, pressure embossing is performed with an embossing roll to obtain a flooring material of the foamed decorative material of the present invention.
【0016】「図2」は本発明発泡装飾材断面図であ
る。1は上層、2は下層、3は複合フィルムであり、8
は印刷層であり、5は発泡層である。発泡層の床下地近
傍に寸法安定性付与のため、厚さ0.1〜0.5mm、
坪量30〜200g/m2の不織布、ネット等の繊維層
9を介在させても良い。このようにして本願他の発泡装
飾材10を得る。このようにして得られた床材は燃焼時
に有毒ガスを発生させず、強度面でもPVCを用いた床
材と比較して遜色がない等、有用なものであった。FIG. 2 is a sectional view of the foam decorative material of the present invention. 1 is an upper layer, 2 is a lower layer, 3 is a composite film, 8
Is a printing layer, and 5 is a foam layer. In order to provide dimensional stability near the floor base of the foam layer, a thickness of 0.1 to 0.5 mm,
A fiber layer 9 such as a nonwoven fabric or a net having a basis weight of 30 to 200 g / m 2 may be interposed. In this way, another foam decorative material 10 of the present application is obtained. The flooring material thus obtained was useful because it did not generate toxic gas during combustion and was comparable in strength to flooring materials using PVC.
【0017】[0017]
【実施例1】50g/m2のガラス不織布の基材上に
「表2」配合で混入した発泡性樹脂を押出機で厚さ約
0.3mmになる様に塗布し、プレヒートオーブンにて
加熱して模様を転写後、その表面に「表3」の上層と下
層からなる複合フィルムをラミネートし、その後メイン
オーブン(200℃)で加熱発泡し、最後にエンボスロ
ールで型押しして厚さ2mmの 発泡床材を得た。得ら
れた床材は、柔軟である、反りがない、白化しない、施
工性がよい,耐摩耗性がよい,耐傷性がよい,等の効果が
あった。Example 1 A foamable resin mixed with a composition shown in Table 2 was applied to a glass nonwoven fabric substrate of 50 g / m 2 so as to have a thickness of about 0.3 mm by an extruder, and heated in a preheat oven. After transferring the pattern, a composite film consisting of an upper layer and a lower layer of “Table 3” was laminated on the surface, and then heated and foamed in a main oven (200 ° C.). A foam flooring material was obtained. The obtained flooring material had effects such as flexibility, no warpage, no whitening, good workability, good wear resistance, and good scratch resistance.
【0018】 (表2) EVA樹脂1 100(単位:PHR) (MFR2g/10min、VAc28%) アゾジカーボンアミド系発泡剤 3.0 ステアリン酸亜鉛 1.0 着色剤(TiO ) 2.0(Table 2) EVA resin 1 100 (unit: PHR) (MFR 2 g / 10 min, VAc 28%) Azodicarbonamide foaming agent 3.0 Zinc stearate 1.0 Colorant (TiO 2) 2.0
【0019】 (表3) 押出しシート=樹脂層 0.3mm 表層フィルム(2層構成) 2層共押 上層 アイオノマー1 MFR 5g/10min 50μm 下層 アイオノマー1 MFR 14g/10min 50μm(Table 3) Extruded sheet = resin layer 0.3 mm Surface film (two-layer structure) Two layers co-pressed Upper layer Ionomer 1 MFR 5 g / 10 min 50 μm Lower layer Ionomer 1 MFR 14 g / 10 min 50 μm
【0020】[0020]
【実施例2】実施例1の発泡性層上に「表4」の上層―
下層の3層の複合フィルムを積層後加熱発泡し、発泡床
材を得た。Example 2 The upper layer of "Table 4" on the foamable layer of Example 1
After laminating the lower three-layer composite film, it was heated and foamed to obtain a foamed floor material.
【0021】 (表4) 押出しシート=樹脂層 0.5mm 表層フィルム(3層構成) 3層インフレ 上層 アイオノマー2 MFR 1g/10min 中間層 アイオノマー2+EVA2=20:80 下層 EVA2 ( Va 28% MFR 6g/10min) 各層40μm(全厚120μm)(Table 4) Extruded sheet = resin layer 0.5 mm Surface layer film (three-layer configuration) Three-layer inflation Upper layer Ionomer 2 MFR 1 g / 10 min Middle layer Ionomer 2 + EVA2 = 20: 80 Lower layer EVA2 (Va 28% MFR 6 g / 10 min ) Each layer 40μm (total thickness 120μm)
【0022】[0022]
【比較例】実施例1の発泡性層上に「表5」の複合フィ
ルムを積層後発泡し、発泡床材を得た。 (表5) 押出しシート=樹脂層 0.5mm 表層フィルム(3層構成) 3層共押 上層 PP / 中間層 PE / 下層 EVA 各層35μm(全厚105μm)COMPARATIVE EXAMPLE The composite film of Table 5 was laminated on the foamable layer of Example 1 and foamed to obtain a foamed floor material. (Table 5) Extruded sheet = Resin layer 0.5 mm Surface layer film (three-layer configuration) Three layers co-pressed Upper layer PP / Intermediate layer PE / Lower layer EVA Each layer 35 μm (total thickness 105 μm)
【表1】 [Table 1]
【0023】折り曲げ白化 表面側に90°折り曲げ、
同じ線で裏面側に90°折り曲げ、折り曲げ部分が白化し
ているものを ×、白化していないものを ○ 施工性 施工台に施工を行い評価を実施。○ 問題無し △ 端部の治まり作業性に難有り 耐傷付き性 表面を布で擦り、傷が無い物を ○、傷が
つき白くなったものを ×Bending whitening 90 ° bending on the surface side,
The same line was bent 90 degrees to the back side, and the one where the bent part was whitened was ×, and the one that was not whitened was ○ Workability. ○ No problem △ End work hardly workability Scratch resistance Surface rubbed with a cloth, no scratches ○, scratched white x
【0024】得られた発泡床材の性能を「表1」に示
す。表5により、20℃でも5℃でも実施例は比較例よ
り柔軟であり、加熱反りも実施例は、比較例の約60%
と低く、寸法及び形態安定性に優れていた。また耐折り
曲げ白化性、施工性も優れた。さらに比較例の耐摩耗性
が0.20mmであるのに対し、本願実施例では半分以
下の0.09mmであり、耐傷付き性にも優れた。Table 1 shows the performance of the obtained foamed floor material. According to Table 5, at 20 ° C. and at 5 ° C., the examples are more flexible than the comparative examples, and the examples show about 60% of the heating warpage of the comparative examples.
Low and excellent in dimensional and morphological stability. In addition, bending whitening resistance and workability were excellent. Furthermore, while the abrasion resistance of the comparative example was 0.20 mm, the abrasion resistance of the example of the present application was 0.09 mm, which is half or less, and the abrasion resistance was excellent.
【0025】[0025]
【発明の効果】 1.柔軟である。 2.反りがない。 3.白化しない 4.施工性がよい。 5.耐摩耗性がよい。 6.耐傷性がよい。Effect of the Invention Be flexible. 2. There is no warpage. 3. Does not whiten Good workability. 5. Good wear resistance. 6. Good scratch resistance.
【図1】 本発明発泡装飾材断面図である。FIG. 1 is a cross-sectional view of the foam decorative material of the present invention.
【図2】 本発明発泡装飾材断面図である。FIG. 2 is a cross-sectional view of the foam decorative material of the present invention.
1 上層 2 下層 3 複合フィルム 5 発泡層 7,10 発泡装飾材 DESCRIPTION OF SYMBOLS 1 Upper layer 2 Lower layer 3 Composite film 5 Foam layer 7,10 Foam decorative material
Claims (2)
ノマーの上層と、該上層よりも柔らかい塩素を含有しな
いフィルムの下層からなる複合フィルムが積層されたこ
とを特徴とする発泡装飾材。1. A foam decorative material comprising a composite film comprising an ionomer upper layer and a chlorine-free film lower than the upper layer, laminated on a chlorine-free resin foam layer.
ー、エチレンー酢酸ビニルコポリマー、ナイロン、アク
リル系樹脂、ポリオレフィンのうちの1種のフィルムで
ある請求項1の発泡装飾材。2. The foam decorative material according to claim 1, wherein the film constituting the lower layer is one of an ionomer, an ethylene-vinyl acetate copolymer, nylon, an acrylic resin, and a polyolefin.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2001027795A JP4695269B2 (en) | 2001-02-05 | 2001-02-05 | Foam decoration |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2001027795A JP4695269B2 (en) | 2001-02-05 | 2001-02-05 | Foam decoration |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2002225201A true JP2002225201A (en) | 2002-08-14 |
JP4695269B2 JP4695269B2 (en) | 2011-06-08 |
Family
ID=18892395
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2001027795A Expired - Fee Related JP4695269B2 (en) | 2001-02-05 | 2001-02-05 | Foam decoration |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP4695269B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006272693A (en) * | 2005-03-29 | 2006-10-12 | Dainippon Printing Co Ltd | Decorative sheet for wall finish |
JP2006272692A (en) * | 2005-03-29 | 2006-10-12 | Dainippon Printing Co Ltd | Decorative sheet for wall finish |
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JPH0542619A (en) * | 1991-08-12 | 1993-02-23 | Du Pont Mitsui Polychem Co Ltd | Laminate and manufacture thereof |
JPH08254004A (en) * | 1995-03-15 | 1996-10-01 | Dainippon Printing Co Ltd | Floor material |
JPH09207276A (en) * | 1995-12-01 | 1997-08-12 | Toppan Printing Co Ltd | Facing material |
JPH11182009A (en) * | 1997-12-24 | 1999-07-06 | Dainippon Printing Co Ltd | Flooring sheet |
JP2001012048A (en) * | 1999-06-30 | 2001-01-16 | Dainippon Printing Co Ltd | Decorative wall sheet |
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2001
- 2001-02-05 JP JP2001027795A patent/JP4695269B2/en not_active Expired - Fee Related
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JPS5529240U (en) * | 1978-08-16 | 1980-02-26 | ||
JPH0542619A (en) * | 1991-08-12 | 1993-02-23 | Du Pont Mitsui Polychem Co Ltd | Laminate and manufacture thereof |
JPH08254004A (en) * | 1995-03-15 | 1996-10-01 | Dainippon Printing Co Ltd | Floor material |
JPH09207276A (en) * | 1995-12-01 | 1997-08-12 | Toppan Printing Co Ltd | Facing material |
JPH11182009A (en) * | 1997-12-24 | 1999-07-06 | Dainippon Printing Co Ltd | Flooring sheet |
JP2001012048A (en) * | 1999-06-30 | 2001-01-16 | Dainippon Printing Co Ltd | Decorative wall sheet |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2006272693A (en) * | 2005-03-29 | 2006-10-12 | Dainippon Printing Co Ltd | Decorative sheet for wall finish |
JP2006272692A (en) * | 2005-03-29 | 2006-10-12 | Dainippon Printing Co Ltd | Decorative sheet for wall finish |
JP4606220B2 (en) * | 2005-03-29 | 2011-01-05 | 大日本印刷株式会社 | Wall decoration sheet |
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