JP2013113022A - Flooring material - Google Patents

Flooring material Download PDF

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JP2013113022A
JP2013113022A JP2011261146A JP2011261146A JP2013113022A JP 2013113022 A JP2013113022 A JP 2013113022A JP 2011261146 A JP2011261146 A JP 2011261146A JP 2011261146 A JP2011261146 A JP 2011261146A JP 2013113022 A JP2013113022 A JP 2013113022A
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resin layer
resin
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flooring
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JP5913932B2 (en
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Takahiro Shibayama
誉宏 柴山
Koji Nishitani
浩二 西谷
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Suminoe Textile Co Ltd
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Abstract

PROBLEM TO BE SOLVED: To provide a flooring material that hardly generates toxic gas in the case of firing, can prevent the occurrence of valley warp, is excellent in workability, can prevent the occurrence of swelling, and can prevent the occurrence of push-up after construction.SOLUTION: A flooring material 1 has a surface resin layer 2 integrally laminated on an upper surface side of an intermediate resin layer 3 and a rear surface resin layer 4 integrally laminated on a lower surface side of the intermediate resin layer 3. The surface resin layer 2, the intermediate resin layer 3, and the rear surface resin layer 4 are such resin layers that only resins without chlorine atoms in a chemical structure as a resin component are substantially used. The surface resin layer 2 is formed by laminating a surface resin sheet with its linear expansion coefficient being 10.0×10/K or lower on the upper surface side of the intermediate resin layer 3. The rear surface resin layer 4 is formed by laminating a rear surface resin sheet with its linear expansion coefficient being 10.0×10/K or lower on the lower surface side of the intermediate resin layer 3. A thickness of the surface resin layer and a thickness of the rear surface resin layer are 0.03 mm to 1.0 mm, respectively. The rear surface resin layer has the thickness 1.0 to 4.0 times that of the surface resin layer.

Description

本発明は、例えば、ビル、マンション、家屋、商業施設等の建築物の床材、或いは鉄道、バス等の車輌の床材として好適に用いられる床材に関する。   The present invention relates to a flooring material suitably used as a flooring material for buildings such as buildings, condominiums, houses, and commercial facilities, or a flooring material for vehicles such as railways and buses.

なお、本明細書では、「ポリプロピレン系樹脂」の語は、エラストマー(即ちポリプロピレン系エラストマー)を含まない意味で用いている。   In the present specification, the term “polypropylene-based resin” is used in a meaning that does not include an elastomer (that is, a polypropylene-based elastomer).

また、本明細書では、「樹脂シート」の語は、「樹脂フィルム」を含む意味で用いている。   In this specification, the term “resin sheet” is used to mean “resin film”.

また、本明細書では、「線膨張率」の語は、JIS K7197−1991に準拠して熱機械測定装置(TMA)を用いて30℃〜60℃の条件下で測定した線膨張率を意味する。   Moreover, in this specification, the term "linear expansion coefficient" means the linear expansion coefficient measured on 30-60 degreeC conditions using the thermomechanical measuring apparatus (TMA) based on JISK7197-1991. To do.

従来、ビル、マンション、家屋、商業施設等の建築物の床材、或いは鉄道、バス等の車輌の床材(タイル状床材、シート状床材)としては、塩化ビニル樹脂(PVC)からなるものが多く採用されていた。   Conventionally, floor materials for buildings such as buildings, condominiums, houses, commercial facilities, or floor materials for vehicles such as railways and buses (tile floor materials, sheet-like floor materials) are made of vinyl chloride resin (PVC). Many things were adopted.

しかしながら、PVC製床材は、燃焼時において多量の発煙と共に有害ガスを発生することから、火災時において避難者が該有害ガス等を吸入してしまう等の防災上の問題、また焼却廃棄処理によって環境汚染をもたらすという問題があった。また、PVC製床材は可塑剤を多量に含有しているので、特有の臭気があるし、長年の使用により可塑剤が揮発減量して床材としての柔軟性が低下するという問題や、長年の使用により可塑剤が表面にブリードして曇りを生じやすく外観体裁が悪くなるという問題もあった。   However, because PVC flooring generates harmful gases along with a large amount of smoke during combustion, there are problems with disaster prevention such as evacuees inhaling harmful gases during a fire, and incineration disposal treatment. There was a problem of causing environmental pollution. In addition, since PVC flooring contains a large amount of plasticizer, there is a peculiar odor, and the long-term use of the plasticizer volatilizes to reduce the flexibility as a flooring. There is also a problem in that the appearance of the plasticizer tends to be fogged on the surface due to the use, and the appearance is poor.

そこで、近年では、PVC材料に代えて、燃焼時に有害ガスの発生が少ない次のような材料を床材の構成材として用いることが提案されている。例えばポリプロピレン樹脂、ポリエチレン樹脂、エチレン−エチルアクリレートコポリマー、エチレン−メチルメタクリレートコポリマー、エチレン−酢酸ビニルコポリマー等のエチレン系コポリマー、ポリブテン−1等のオレフィン系熱可塑性樹脂、ポリメチルメタクリレート、ポリメチルメタクリレートとアクリルゴムとのコポリマー等のアクリル系熱可塑性樹脂、ポリウレタン系熱可塑性樹脂、オレフィン系熱可塑性エラストマー、スチレン系熱可塑性エラストマー、ウレタン系熱可塑性エラストマー等を床材の構成材として用いることが提案されている(特許文献1、2参照)。これらの樹脂を床材の構成材として用いることで、燃焼時の有害ガスの発生の問題や、可塑剤由来の特有の臭気、曇り発生の問題はほぼ解決される。   Therefore, in recent years, it has been proposed to use the following materials, which generate less harmful gases during combustion, instead of PVC materials as constituent materials for flooring. For example, polypropylene resin, polyethylene resin, ethylene-ethyl acrylate copolymer, ethylene-methyl methacrylate copolymer, ethylene-based copolymer such as ethylene-vinyl acetate copolymer, olefin-based thermoplastic resin such as polybutene-1, polymethyl methacrylate, polymethyl methacrylate and acrylic It has been proposed to use acrylic thermoplastic resins such as copolymers with rubber, polyurethane thermoplastic resins, olefin thermoplastic elastomers, styrene thermoplastic elastomers, urethane thermoplastic elastomers, etc. as constituents of flooring materials. (See Patent Documents 1 and 2). By using these resins as the constituent material of the flooring, the problem of generation of harmful gases during combustion, the peculiar odor caused by the plasticizer, and the problem of clouding are almost solved.

特開2002−145942号公報JP 2002-145942 A 特開2002−105874号公報JP 2002-105874 A

しかしながら、上記後者の従来技術では、床材の谷反り現象(中央部に対して縁部側が上方に反る状態)を十分に防止できるものではなく、このために施工性に劣っていた。また、上記後者の従来技術では、床材に膨れ発生を生じることが懸念される上に、施工後において突き上げ現象が発生しやすいという問題もあった。   However, in the latter prior art, the floor warping phenomenon of the flooring (a state in which the edge side warps upward with respect to the central portion) cannot be sufficiently prevented, and therefore, the workability is inferior. In the latter prior art, there is a concern that the flooring may be swollen, and a push-up phenomenon is likely to occur after construction.

本発明は、かかる技術的背景に鑑みてなされたものであって、燃焼時に有害ガスを発生しにくく、谷反り発生を十分に防止でき、施工性に優れると共に、膨れ発生を抑制することができ、且つ施工後の突き上げ発生も防止できる床材を提供することを目的とする。   The present invention has been made in view of such a technical background, and it is difficult to generate harmful gas during combustion, can sufficiently prevent the occurrence of valley warp, has excellent workability, and can suppress the occurrence of swelling. And it aims at providing the flooring which can also prevent the pushing-up generation | occurrence | production after construction.

前記目的を達成するために、本発明は以下の手段を提供する。   In order to achieve the above object, the present invention provides the following means.

[1]中間樹脂層の上面側に表面樹脂層が積層一体化され、前記中間樹脂層の下面側に裏面樹脂層が積層一体化されてなる床材であって、
前記表面樹脂層、前記中間樹脂層及び前記裏面樹脂層は、樹脂成分として、化学構造中に塩素原子を有しない樹脂のみが実質的に用いられてなる樹脂層であり、
前記表面樹脂層は、線膨張率が10.0×10-5/K以下である表面樹脂シートが前記中間樹脂層の上面側に積層されたものであり、
前記裏面樹脂層は、線膨張率が10.0×10-5/K以下である裏面樹脂シートが前記中間樹脂層の下面側に積層されたものであり、
前記表面樹脂層の厚さは0.03mm〜1.0mmであり、前記裏面樹脂層の厚さは0.03mm〜1.0mmであり、前記裏面樹脂層の厚さは、前記表面樹脂層の厚さの1.0倍〜4.0倍の範囲であることを特徴とする床材。
[1] A flooring material in which a surface resin layer is laminated and integrated on an upper surface side of an intermediate resin layer, and a back surface resin layer is laminated and integrated on a lower surface side of the intermediate resin layer,
The surface resin layer, the intermediate resin layer, and the back resin layer are resin layers in which only a resin having no chlorine atom in the chemical structure is substantially used as a resin component,
The surface resin layer is obtained by laminating a surface resin sheet having a linear expansion coefficient of 10.0 × 10 −5 / K or less on the upper surface side of the intermediate resin layer,
The back resin layer is obtained by laminating a back resin sheet having a linear expansion coefficient of 10.0 × 10 −5 / K or less on the lower surface side of the intermediate resin layer,
The thickness of the surface resin layer is 0.03 mm to 1.0 mm, the thickness of the back surface resin layer is 0.03 mm to 1.0 mm, and the thickness of the back surface resin layer is the thickness of the surface resin layer. A flooring material having a thickness in the range of 1.0 to 4.0 times the thickness.

[2]前記表面樹脂層及び前記裏面樹脂層は、樹脂成分の主成分として、非晶性ポリエステル樹脂が用いられている前項1に記載の床材。   [2] The flooring according to the above item 1, wherein the surface resin layer and the back surface resin layer are made of an amorphous polyester resin as a main component of the resin component.

[3]前記中間樹脂層は、ガラス基布層と、該ガラス基布層の上面側に積層された上側中間樹脂層と、前記ガラス基布層の下面側に積層された下側中間樹脂層と、を含み、
前記上側中間樹脂層及び前記下側中間樹脂層は、樹脂成分として、化学構造中に塩素原子を有しない樹脂のみが実質的に用いられてなる樹脂層であることを特徴とする前項1または2に記載の床材。
[3] The intermediate resin layer includes a glass base fabric layer, an upper intermediate resin layer stacked on the upper surface side of the glass base fabric layer, and a lower intermediate resin layer stacked on the lower surface side of the glass base fabric layer. And including
1 or 2 above, wherein the upper intermediate resin layer and the lower intermediate resin layer are resin layers in which only a resin having no chlorine atom in the chemical structure is substantially used as a resin component. The flooring described in 1.

[4]前記上側中間樹脂層及び前記下側中間樹脂層は、樹脂成分として、ポリプロピレン系エラストマー及びポリプロピレン系樹脂が用いられている前項3に記載の床材。   [4] The flooring according to the above item 3, wherein the upper intermediate resin layer and the lower intermediate resin layer use polypropylene elastomer and polypropylene resin as resin components.

[5]前記表面樹脂層の下面に印刷層が形成され、該印刷層の下面にカルボン酸変性ポリオレフィン樹脂を含有してなるプライマー塗布層が形成されている前項1〜4のいずれか1項に記載の床材。   [5] In any one of the above items 1 to 4, wherein a printed layer is formed on the lower surface of the surface resin layer, and a primer coating layer containing a carboxylic acid-modified polyolefin resin is formed on the lower surface of the printed layer. The flooring described.

[1]の発明では、表面樹脂層、中間樹脂層及び裏面樹脂層は、樹脂成分として、化学構造中に塩素原子を有しない樹脂のみが実質的に用いられてなる樹脂層であるから、燃焼時の有害ガスの発生が少なく、燃焼安全性に優れて防災面で好都合であると共に環境保全にも十分に資することができる。また、表面樹脂層は、線膨張率が10.0×10-5/K以下である表面樹脂シートが中間樹脂層の上面側に積層されたものであり、裏面樹脂層は、線膨張率が10.0×10-5/K以下である裏面樹脂シートが中間樹脂層の下面側に積層されたものであるから、谷反り発生を十分に防止できるし、施工性にも優れる上に、膨れ発生を抑制でき、且つ施工後の突き上げ発生も防止できる。 In the invention of [1], the front surface resin layer, the intermediate resin layer, and the back surface resin layer are resin layers in which only a resin having no chlorine atom in the chemical structure is substantially used as a resin component. There is little generation of harmful gas at the time, it is excellent in combustion safety, is convenient in terms of disaster prevention, and can fully contribute to environmental conservation. Further, the surface resin layer is obtained by laminating a surface resin sheet having a linear expansion coefficient of 10.0 × 10 −5 / K or less on the upper surface side of the intermediate resin layer, and the back surface resin layer has a linear expansion coefficient. Since a back surface resin sheet of 10.0 × 10 −5 / K or less is laminated on the lower surface side of the intermediate resin layer, it is possible to sufficiently prevent the occurrence of valley warp and excellent workability, and also swell Generation | occurrence | production can be suppressed and the pushing-up generation | occurrence | production after construction can also be prevented.

更に、表面樹脂層の厚さは0.03mm〜1.0mmであり、前記裏面樹脂層の厚さは0.03mm〜1.0mmであるから、床材の寸法安定性を向上できると共に、床材としての柔軟性をさらに向上できて施工性をより向上させることができる。   Furthermore, since the thickness of the surface resin layer is 0.03 mm to 1.0 mm and the thickness of the back surface resin layer is 0.03 mm to 1.0 mm, the dimensional stability of the flooring can be improved, and the floor The flexibility as a material can be further improved and the workability can be further improved.

加えて、裏面樹脂層の厚さは、表面樹脂層の厚さの1.0倍〜4.0倍であるから、谷反り発生をより十分に防止できる。   In addition, since the thickness of the back surface resin layer is 1.0 to 4.0 times the thickness of the surface resin layer, generation of valley warp can be more sufficiently prevented.

[2]の発明では、表面樹脂層及び裏面樹脂層は、樹脂成分の主成分として、非晶性ポリエステル樹脂が用いられてなる構成であるから、表面樹脂シートと裏面樹脂シートの線膨張率をそれぞれ10.0×10-5/K以下の範囲内でより小さくすることができ、これにより、谷反り発生をより十分に防止できるし、施工性をさらに向上できると共に、膨れ発生を十分に抑制できるし、施工後の突き上げ発生も十分に防止できる。 In the invention of [2], since the surface resin layer and the back surface resin layer are composed of an amorphous polyester resin as a main component of the resin component, the linear expansion coefficients of the surface resin sheet and the back surface resin sheet are determined. Each can be made smaller within a range of 10.0 × 10 −5 / K or less, thereby preventing the warp generation more sufficiently, further improving the workability, and sufficiently suppressing the occurrence of swelling. It is possible to prevent the occurrence of push-up after construction.

なお、前記「主成分」の語は、樹脂成分の合計質量に占める割合が50質量%以上100質量%以下である成分を意味するものである。樹脂成分が1成分のみである場合にはその1成分を「主成分」と言うものとする。   The term “main component” means a component having a ratio of 50% by mass to 100% by mass with respect to the total mass of the resin components. When the resin component is only one component, the one component is referred to as “main component”.

[3]の発明では、上側中間樹脂層と下側中間樹脂層の間にガラス基布層が積層配置されているから、床材の寸法安定性を向上させることができる。   In the invention [3], since the glass base fabric layer is laminated between the upper intermediate resin layer and the lower intermediate resin layer, the dimensional stability of the flooring can be improved.

[4]の発明では、上側中間樹脂層及び下側中間樹脂層は、樹脂成分として、ポリプロピレン系エラストマー及びポリプロピレン系樹脂が用いられているから、床材としての柔軟性を向上させることができて施工性をさらに向上できると共に、床材を曲げても割れを生じない十分な硬さを付与することができる。   In the invention of [4], since the upper intermediate resin layer and the lower intermediate resin layer use polypropylene elastomer and polypropylene resin as the resin component, the flexibility as a flooring material can be improved. Workability can be further improved, and sufficient hardness that does not cause cracking even when the flooring is bent can be imparted.

[5]の発明では、表面樹脂層の下面に形成された印刷層の下面にカルボン酸変性ポリオレフィン樹脂を含有してなるプライマー塗布層が形成されているから、裏面に印刷層が設けられた表面樹脂層と、中間樹脂層との間の密着性を十分に向上させることができ、耐久性に優れた床材が提供される。   In the invention of [5], since the primer coating layer containing the carboxylic acid-modified polyolefin resin is formed on the lower surface of the printing layer formed on the lower surface of the surface resin layer, the surface on which the printing layer is provided on the back surface Adhesiveness between the resin layer and the intermediate resin layer can be sufficiently improved, and a flooring excellent in durability is provided.

本発明に係る床材の一実施形態を示す断面図である。It is sectional drawing which shows one Embodiment of the flooring which concerns on this invention.

本発明に係る床材の一実施形態を図面に基づいて説明する。図1に示すように、本実施形態の床材1は、中間樹脂層3の上面側に表面樹脂層2が積層一体化され、前記中間樹脂層3の下面側に裏面樹脂層4が積層一体化されてなる床材であり、前記表面樹脂層2、前記中間樹脂層3及び前記裏面樹脂層4は、いずれも、樹脂成分として、化学構造中に塩素原子を有しない樹脂のみが実質的に用いられてなる樹脂層であり、前記表面樹脂層2は、線膨張率が10.0×10-5/K以下である表面樹脂シートが前記中間樹脂層3の上面側に積層されたものであり、前記裏面樹脂層4は、線膨張率が10.0×10-5/K以下である裏面樹脂シートが前記中間樹脂層3の下面側に積層された構成である。 An embodiment of a flooring according to the present invention will be described with reference to the drawings. As shown in FIG. 1, in the flooring 1 of the present embodiment, the surface resin layer 2 is laminated and integrated on the upper surface side of the intermediate resin layer 3, and the back surface resin layer 4 is laminated and integrated on the lower surface side of the intermediate resin layer 3. The surface resin layer 2, the intermediate resin layer 3 and the back resin layer 4 are all made of only a resin having no chlorine atom in the chemical structure as a resin component. The surface resin layer 2 is a resin layer formed by laminating a surface resin sheet having a linear expansion coefficient of 10.0 × 10 −5 / K or less on the upper surface side of the intermediate resin layer 3. The back resin layer 4 has a configuration in which a back resin sheet having a linear expansion coefficient of 10.0 × 10 −5 / K or less is laminated on the lower surface side of the intermediate resin layer 3.

更に、本実施形態では、前記中間樹脂層3は、ガラス基布層12と、該ガラス基布層12の上面に積層された上側中間樹脂層11と、前記ガラス基布層12の下面に積層された下側中間樹脂層13と、からなる。前記上側中間樹脂層11及び前記下側中間樹脂層13は、樹脂成分として、化学構造中に塩素原子を有しない樹脂のみが実質的に用いられてなる樹脂層である。   Further, in the present embodiment, the intermediate resin layer 3 is laminated on the glass base fabric layer 12, the upper intermediate resin layer 11 laminated on the upper surface of the glass base fabric layer 12, and the lower surface of the glass base fabric layer 12. The lower intermediate resin layer 13. The upper intermediate resin layer 11 and the lower intermediate resin layer 13 are resin layers in which only a resin having no chlorine atom in the chemical structure is substantially used as a resin component.

前記中間樹脂層3は、樹脂成分として、化学構造中に塩素原子を有しない樹脂のみが実質的に用いられてなる樹脂層である。前記中間樹脂層3は、単層で構成されていてもよいし、複数層で形成されていてもよい。   The intermediate resin layer 3 is a resin layer in which only a resin having no chlorine atom in the chemical structure is substantially used as a resin component. The intermediate resin layer 3 may be composed of a single layer or a plurality of layers.

中でも、前記中間樹脂層3は、ガラス基布層12と、該ガラス基布層12の上面側に積層された上側中間樹脂層11と、前記ガラス基布層12の下面側に積層された下側中間樹脂層13と、を含む構成であるのが好ましい。   Among them, the intermediate resin layer 3 includes a glass base fabric layer 12, an upper intermediate resin layer 11 laminated on the upper surface side of the glass base fabric layer 12, and a lower layer laminated on the lower surface side of the glass base fabric layer 12. The side intermediate resin layer 13 is preferably included.

この時、上側中間樹脂層11の厚さ/下側中間樹脂層13の厚さ=1.0/1.0〜1.0/3.0の範囲に設定されるのが好ましい。この場合には、床材1の谷反り発生をより十分に防止できる。   At this time, the thickness of the upper intermediate resin layer 11 / the thickness of the lower intermediate resin layer 13 is preferably set in a range of 1.0 / 1.0 to 1.0 / 3.0. In this case, the generation of valley warp of the flooring 1 can be more sufficiently prevented.

前記中間樹脂層3(上側中間樹脂層11、下側中間樹脂層13等)を構成する樹脂成分としては、特に限定されるものではないが、例えば、ポリプロピレン系エラストマー、ポリプロピレン系樹脂、ポリエチレン系エラストマー、ポリエチレン系樹脂等が挙げられる。中でも、前記中間樹脂層3(上側中間樹脂層11、下側中間樹脂層13等)を構成する樹脂成分としては、ポリプロピレン系エラストマー及びポリプロピレン系樹脂を用いるのが好ましい。   The resin component constituting the intermediate resin layer 3 (upper intermediate resin layer 11, lower intermediate resin layer 13 and the like) is not particularly limited, and examples thereof include polypropylene elastomers, polypropylene resins, and polyethylene elastomers. And polyethylene resins. Among these, as the resin component constituting the intermediate resin layer 3 (the upper intermediate resin layer 11, the lower intermediate resin layer 13, etc.), it is preferable to use a polypropylene-based elastomer and a polypropylene-based resin.

前記中間樹脂層3(上側中間樹脂層11、下側中間樹脂層13等)において、ポリプロピレン系エラストマーとポリプロピレン系樹脂の配合質量比は、ポリプロピレン系エラストマー/ポリプロピレン系樹脂=55/5〜25/35の範囲に設定するのが好ましい。このような範囲に設定することにより、床材としての柔軟性を向上させることができて施工性をさらに向上できると共に、床材を曲げても割れを生じない十分な硬さを付与することができる。中でも、ポリプロピレン系エラストマーとポリプロピレン系樹脂の配合質量比は、ポリプロピレン系エラストマー/ポリプロピレン系樹脂=50/10〜35/25の範囲に設定するのが特に好ましい。   In the intermediate resin layer 3 (upper intermediate resin layer 11, lower intermediate resin layer 13, etc.), the blending mass ratio of the polypropylene elastomer to the polypropylene resin is polypropylene elastomer / polypropylene resin = 55/5 to 25/35. It is preferable to set in the range. By setting in such a range, the flexibility as a flooring material can be improved and the workability can be further improved, and sufficient hardness that does not cause cracking even when the flooring material is bent can be imparted. it can. Especially, it is especially preferable to set the blending mass ratio of the polypropylene-based elastomer and the polypropylene-based resin within the range of polypropylene-based elastomer / polypropylene-based resin = 50/10 to 35/25.

前記ポリプロピレン系樹脂としては、特に限定されるものではないが、例えば、エチレン−プロピレン共重合体樹脂、ホモポリプロピレン樹脂(プロピレンの単独重合体)等が挙げられる。   The polypropylene resin is not particularly limited, and examples thereof include an ethylene-propylene copolymer resin and a homopolypropylene resin (a homopolymer of propylene).

前記中間樹脂層3(上側中間樹脂層11、下側中間樹脂層13等)には、充填材(例えば炭酸カルシウム等)、その他の添加剤等を配合してもよい。   The intermediate resin layer 3 (upper intermediate resin layer 11, lower intermediate resin layer 13 and the like) may be blended with a filler (for example, calcium carbonate) and other additives.

前記中間樹脂層3の一部を構成するガラス基布層12としては、特に限定されるものではないが、例えば、ガラス不織布、ガラス織布などが挙げられる。中でも、ガラス不織布を用いるのが好ましく、この場合には、上側中間樹脂層11及び下側中間樹脂層13がガラス基布層(ガラス不織布層)12に含浸しやすく層間剥離強度がさらに向上させることができる。   Although it does not specifically limit as the glass base fabric layer 12 which comprises a part of said intermediate resin layer 3, For example, a glass nonwoven fabric, a glass woven fabric, etc. are mentioned. Among these, it is preferable to use a glass nonwoven fabric. In this case, the upper intermediate resin layer 11 and the lower intermediate resin layer 13 can easily impregnate the glass base fabric layer (glass nonwoven fabric layer) 12 to further improve the delamination strength. Can do.

前記ガラス基布層12の目付としては、20g/m2〜200g/m2に設定されるのが好ましい。20g/m2以上とすることで熱寸法安定性を向上させることができると共に、200g/m2以下とすることで接着性試験(JIS A5536 5.3.3 はくり接着強さに準拠)でこのガラス基布層12の材料破壊が生じないようにすることができる。中でも、前記ガラス基布層12の目付は、50g/m2〜120g/m2に設定されるのがより好ましい。 The basis weight of the glass base fabric layer 12 is preferably set to 20g / m 2 ~200g / m 2 . Thermal dimensional stability can be improved by setting it to 20 g / m 2 or more, and adhesion test (based on peel adhesion strength according to JIS A5536 5.3.3) by setting it to 200 g / m 2 or less. It is possible to prevent the material destruction of the glass base fabric layer 12 from occurring. Above all, the basis weight of said glass base fabric layer 12 is more preferably set to 50g / m 2 ~120g / m 2 .

前記表面樹脂層2は、樹脂成分として、化学構造中に塩素原子を有しない樹脂のみが実質的に用いられてなる樹脂層である。また、前記表面樹脂層2は、線膨張率が10.0×10-5/K以下である表面樹脂シートが前記中間樹脂層3の上面側に積層されたものである。前記表面樹脂層2は、単層で構成されていてもよいし、複数層で形成されていてもよい。前記表面樹脂層2を形成するための、線膨張率が10.0×10-5/K以下である樹脂としては、特に限定されるものではないが、例えば、線膨張率が10.0×10-5/K以下の非晶性ポリエステル樹脂等が挙げられる。しかして、前記表面樹脂層2は、樹脂成分の主成分として、非晶性ポリエステル樹脂が用いられてなる構成であるのが好ましい。前記表面樹脂層2は、樹脂成分の80質量%以上100質量%以下が非晶性ポリエステル樹脂である構成がより好ましい。前記非晶性ポリエステル樹脂としては、例えば、非晶性ポリエチレンテレフタレート(線膨張率が7.2×10-5/K;リケンテクノス社製「PETG」)等を例示できる。中でも、前記表面樹脂層2は、線膨張率が8.0×10-5/K以下である表面樹脂シートが前記中間樹脂層3の上面側に積層されたものであるのが好ましい。 The surface resin layer 2 is a resin layer in which only a resin having no chlorine atom in the chemical structure is substantially used as a resin component. The surface resin layer 2 is obtained by laminating a surface resin sheet having a linear expansion coefficient of 10.0 × 10 −5 / K or less on the upper surface side of the intermediate resin layer 3. The surface resin layer 2 may be composed of a single layer or a plurality of layers. The resin having a linear expansion coefficient of 10.0 × 10 −5 / K or less for forming the surface resin layer 2 is not particularly limited. For example, the linear expansion coefficient is 10.0 × 10 × Examples thereof include amorphous polyester resins of 10 −5 / K or less. Therefore, the surface resin layer 2 preferably has a configuration in which an amorphous polyester resin is used as a main component of the resin component. The surface resin layer 2 is more preferably configured such that 80% by mass or more and 100% by mass or less of the resin component is an amorphous polyester resin. Examples of the amorphous polyester resin include amorphous polyethylene terephthalate (linear expansion coefficient is 7.2 × 10 −5 / K; “PETG” manufactured by Riken Technos). Among them, the surface resin layer 2 is preferably a surface resin sheet having a linear expansion coefficient of 8.0 × 10 −5 / K or less laminated on the upper surface side of the intermediate resin layer 3.

前記表面樹脂層2の厚さは0.03mm〜1.0mmに設定される。中でも、前記表面樹脂層2の厚さは0.05mm〜0.5mmに設定されるのが好ましい。   The thickness of the surface resin layer 2 is set to 0.03 mm to 1.0 mm. Especially, it is preferable that the thickness of the surface resin layer 2 is set to 0.05 mm to 0.5 mm.

前記表面樹脂層2の下面に印刷層を積層してもよい。この場合、前記印刷層の下面にプライマー塗布層が形成されているのが好ましい。このようなプライマー塗布層を形成することによって、前記表面樹脂層2と前記中間樹脂層3との接着強度を向上させることができる。前記プライマー塗布層は、カルボン酸変性ポリオレフィン樹脂を含有してなるプライマー塗布層であるのが好ましい。前記印刷層は、例えば、インクジェット法、グラビア印刷法、スクリーン印刷法、転写印刷法等により形成することができる。   A printed layer may be laminated on the lower surface of the surface resin layer 2. In this case, it is preferable that a primer coating layer is formed on the lower surface of the printing layer. By forming such a primer coating layer, the adhesive strength between the surface resin layer 2 and the intermediate resin layer 3 can be improved. The primer coating layer is preferably a primer coating layer containing a carboxylic acid-modified polyolefin resin. The printing layer can be formed by, for example, an inkjet method, a gravure printing method, a screen printing method, a transfer printing method, or the like.

前記裏面樹脂層4は、樹脂成分として、化学構造中に塩素原子を有しない樹脂のみが実質的に用いられてなる樹脂層である。また、前記裏面樹脂層4は、線膨張率が10.0×10-5/K以下である裏面樹脂シートが前記中間樹脂層3の下面側に積層されたものである。前記裏面樹脂層4は、単層で構成されていてもよいし、複数層で形成されていてもよい。前記裏面樹脂層4を形成するための、線膨張率が10.0×10-5/K以下である樹脂としては、特に限定されるものではないが、例えば、線膨張率が10.0×10-5/K以下の非晶性ポリエステル樹脂等が挙げられる。しかして、前記裏面樹脂層4は、樹脂成分の主成分として、非晶性ポリエステル樹脂が用いられてなる構成であるのが好ましい。前記裏面樹脂層4は、樹脂成分の80質量%以上100質量%以下が非晶性ポリエステル樹脂である構成がより好ましい。前記非晶性ポリエステル樹脂としては、例えば、非晶性ポリエチレンテレフタレート(線膨張率が7.2×10-5/K;リケンテクノス社製「PETG」)等を例示できる。中でも、前記裏面樹脂層4は、線膨張率が8.0×10-5/K以下である裏面樹脂シートが前記中間樹脂層3の下面側に積層されたものであるのが好ましい。 The back resin layer 4 is a resin layer in which only a resin having no chlorine atom in the chemical structure is substantially used as a resin component. In addition, the back surface resin layer 4 is obtained by laminating a back surface resin sheet having a linear expansion coefficient of 10.0 × 10 −5 / K or less on the lower surface side of the intermediate resin layer 3. The said back surface resin layer 4 may be comprised by the single layer, and may be formed by the multiple layer. The resin having a linear expansion coefficient of 10.0 × 10 −5 / K or less for forming the back surface resin layer 4 is not particularly limited. For example, the linear expansion coefficient is 10.0 × 10 × Examples thereof include amorphous polyester resins of 10 −5 / K or less. Therefore, the back surface resin layer 4 preferably has a configuration in which an amorphous polyester resin is used as a main component of the resin component. As for the said back surface resin layer 4, the structure whose 80 to 100 mass% of a resin component is an amorphous polyester resin is more preferable. Examples of the amorphous polyester resin include amorphous polyethylene terephthalate (linear expansion coefficient is 7.2 × 10 −5 / K; “PETG” manufactured by Riken Technos). Especially, it is preferable that the back surface resin layer 4 has a back surface resin sheet having a linear expansion coefficient of 8.0 × 10 −5 / K or less laminated on the lower surface side of the intermediate resin layer 3.

前記裏面樹脂層4の厚さは0.03mm〜1.0mmに設定される。中でも、前記裏面樹脂層4の厚さは0.05mm〜0.5mmに設定されるのが好ましい。   The thickness of the back surface resin layer 4 is set to 0.03 mm to 1.0 mm. Especially, it is preferable that the thickness of the said back surface resin layer 4 is set to 0.05 mm-0.5 mm.

前記裏面樹脂層4の上面にプライマー塗布層が形成されているのが好ましい。このようなプライマー塗布層を形成することによって、裏面樹脂層4と中間樹脂層3との接着強度を向上させることができる。前記裏面樹脂層4の上面のプライマー塗布層は、カルボン酸変性ポリオレフィン樹脂を含有してなるプライマー塗布層であるのが好ましい。   A primer coating layer is preferably formed on the upper surface of the back surface resin layer 4. By forming such a primer coating layer, the adhesive strength between the back surface resin layer 4 and the intermediate resin layer 3 can be improved. The primer coating layer on the upper surface of the back surface resin layer 4 is preferably a primer coating layer containing a carboxylic acid-modified polyolefin resin.

前記裏面樹脂層4の下面にプライマー塗布層が形成されているのが好ましい。これにより、施工時の敷設対象面に塗布される接着剤との接着性を向上させることができる。この裏面樹脂層4の下面のプライマー塗布層は、カルボン酸変性ポリオレフィン樹脂を含有してなるプライマー塗布層であるのが好ましい。   A primer coating layer is preferably formed on the lower surface of the back surface resin layer 4. Thereby, adhesiveness with the adhesive agent apply | coated to the installation object surface at the time of construction can be improved. The primer coating layer on the lower surface of the back surface resin layer 4 is preferably a primer coating layer containing a carboxylic acid-modified polyolefin resin.

本発明において、前記裏面樹脂層4の厚さは、前記表面樹脂層2の厚さの1.0倍〜4.0倍の範囲に設定される。このような範囲に設定することにより、床材の谷反り発生をより十分に防止できる。中でも、前記裏面樹脂層4の厚さは、前記表面樹脂層2の厚さの1.5倍〜3.0倍の範囲であるのが好ましい。   In the present invention, the thickness of the back surface resin layer 4 is set in a range of 1.0 to 4.0 times the thickness of the surface resin layer 2. By setting to such a range, generation | occurrence | production of the valley warp of a flooring can be prevented more fully. Especially, it is preferable that the thickness of the said back surface resin layer 4 is the range of 1.5 times-3.0 times the thickness of the said surface resin layer 2. FIG.

前記表面樹脂層2,中間樹脂層3、裏面樹脂層4のいずれにも、酸化防止剤、紫外線吸収剤、滑剤、熱安定剤、光安定剤、難燃剤、着色剤、帯電防止剤等の各種添加剤を適宜含有せしめてもよい。   For each of the front surface resin layer 2, the intermediate resin layer 3, and the back surface resin layer 4, various kinds of antioxidants, ultraviolet absorbers, lubricants, heat stabilizers, light stabilizers, flame retardants, colorants, antistatic agents, etc. You may make it contain an additive suitably.

本発明の床材1の厚さは、特に限定されないものの、1.0mm〜4.0mmに設定されるのが好ましい。   The thickness of the flooring 1 of the present invention is not particularly limited, but is preferably set to 1.0 mm to 4.0 mm.

本発明の床材1は、タイル状床材として構成しても良いし、シート状床材(例えば幅600〜2500mm程度の長尺シート等)として構成しても良く、特に限定されない。   The flooring 1 of the present invention may be configured as a tile-shaped flooring or a sheet-like flooring (for example, a long sheet having a width of about 600 to 2500 mm), and is not particularly limited.

本発明に係る床材の製造方法としては、特に限定されず、例えばカレンダ加工機、押出加工機等の公知の装置や、ホットラミネート加工機等の公知の積層技術を用いて積層することにより製造することができる。また、その積層順序も特に限定されない。   The method for producing the flooring according to the present invention is not particularly limited, and for example, it is produced by laminating using a known laminating technique such as a known machine such as a calendering machine or an extruder or a hot laminating machine. can do. Further, the stacking order is not particularly limited.

次に、本発明の具体的実施例について説明するが、本発明はこれら実施例のものに特に限定されるものではない。   Next, specific examples of the present invention will be described, but the present invention is not particularly limited to these examples.

<実施例1>
ポリプロピレン系エラストマー45質量部、ポリプロピレン系樹脂15質量部、炭酸カルシウム40質量部からなる樹脂組成物をバンバリーミキサーで混練し、カレンダー成形機を用いて、厚さ0.9mmの上側中間シート(上側中間樹脂層11)および厚さ0.9mmの下側中間シート(下側中間樹脂層13)をそれぞれ作製した。
<Example 1>
A resin composition comprising 45 parts by mass of a polypropylene-based elastomer, 15 parts by mass of a polypropylene-based resin, and 40 parts by mass of calcium carbonate was kneaded with a Banbury mixer, and the upper intermediate sheet (upper Resin layer 11) and a lower intermediate sheet having a thickness of 0.9 mm (lower intermediate resin layer 13) were prepared.

また、表面樹脂シート(表面樹脂層2)として、線膨張率が7.2×10-5/Kで厚さ0.1mmの非晶性ポリエチレンテレフタレート樹脂フィルム(リケンテクノス社製「PETG」)を準備し、裏面樹脂シート(裏面樹脂層4)として、線膨張率が7.2×10-5/Kで厚さ0.2mmの非晶性ポリエチレンテレフタレート樹脂フィルム(リケンテクノス社製「PETG」)を準備した。なお、表面樹脂シートの裏面にグラビア印刷を行って印刷層を形成し、該印刷層にカルボン酸変性ポリオレフィン樹脂を含有してなるプライマー液を塗布してプライマー塗布層を形成した。 In addition, as the surface resin sheet (surface resin layer 2), an amorphous polyethylene terephthalate resin film (“PETG” manufactured by Riken Technos) having a linear expansion coefficient of 7.2 × 10 −5 / K and a thickness of 0.1 mm is prepared. Then, an amorphous polyethylene terephthalate resin film (“PETG” manufactured by Riken Technos) having a linear expansion coefficient of 7.2 × 10 −5 / K and a thickness of 0.2 mm is prepared as the back surface resin sheet (back surface resin layer 4). did. In addition, gravure printing was performed on the back surface of the front surface resin sheet to form a printing layer, and a primer solution containing a carboxylic acid-modified polyolefin resin was applied to the printing layer to form a primer coating layer.

下側から、裏面樹脂シート、下側中間シート、ガラス不織布(目付60g/m2)、上側中間シートおよび表面樹脂シート(印刷層、プライマー塗布層が下側になる配置)を、この順に重ねて、熱プレス機を用いて150℃、1.0MPaの条件で5分間圧縮成形を行うことによって、図1に示す厚さ2.0mmの床材1を得た。 From the lower side, the back side resin sheet, the lower side intermediate sheet, the glass nonwoven fabric (weight per unit: 60 g / m 2 ), the upper side intermediate sheet and the surface resin sheet (arrangement where the printing layer and primer coating layer are on the lower side) are stacked in this order. The flooring 1 having a thickness of 2.0 mm shown in FIG. 1 was obtained by compression molding using a hot press machine at 150 ° C. and 1.0 MPa for 5 minutes.

<実施例2>
裏面樹脂層の厚さを0.3mmに設定し、裏面樹脂層の厚さ/表面樹脂層の厚さ=3.0に設定した以外は、実施例1と同様にして厚さ2.1mmの床材を得た。
<Example 2>
The thickness of the back surface resin layer was set to 0.3 mm, and the thickness of the back surface resin layer / the thickness of the front surface resin layer was set to 3.0 as in Example 1 except that the thickness was set to 2.1 mm. A flooring was obtained.

<実施例3>
裏面樹脂層の厚さを0.15mmに設定し、裏面樹脂層の厚さ/表面樹脂層の厚さ=1.5に設定した以外は、実施例1と同様にして厚さ1.95mmの床材を得た。
<Example 3>
The thickness of the back surface resin layer was set to 0.15 mm, and the thickness of the back surface resin layer / the thickness of the front surface resin layer was set to 1.5. A flooring was obtained.

<実施例4>
上側中間樹脂層及び下側中間樹脂層を構成する樹脂組成物として、ポリプロピレン系エラストマー35質量部、ポリプロピレン系樹脂25質量部および炭酸カルシウム40質量部を配合して得られた樹脂組成物を用いた以外は、実施例1と同様にして厚さ2.0mmの床材を得た。
<Example 4>
As a resin composition constituting the upper intermediate resin layer and the lower intermediate resin layer, a resin composition obtained by blending 35 parts by mass of a polypropylene elastomer, 25 parts by mass of a polypropylene resin and 40 parts by mass of calcium carbonate was used. Except for this, a flooring material having a thickness of 2.0 mm was obtained in the same manner as in Example 1.

<実施例5>
上側中間樹脂層及び下側中間樹脂層を構成する樹脂組成物として、ポリプロピレン系エラストマー15質量部、ポリプロピレン系樹脂45質量部および炭酸カルシウム40質量部を配合して得られた樹脂組成物を用いた以外は、実施例1と同様にして厚さ2.0mmの床材を得た。
<Example 5>
As a resin composition constituting the upper intermediate resin layer and the lower intermediate resin layer, a resin composition obtained by blending 15 parts by mass of a polypropylene elastomer, 45 parts by mass of a polypropylene resin and 40 parts by mass of calcium carbonate was used. Except for this, a flooring material having a thickness of 2.0 mm was obtained in the same manner as in Example 1.

<実施例6>
表面樹脂シートとして、線膨張率が9.1×10-5/Kで厚さが0.1mmのオレフィン系樹脂フィルム(オレフィン系樹脂35質量部、金属水酸化物塩60質量部、層状珪酸塩5質量部からなる樹脂組成物のフィルム)を用い、裏面樹脂シートとして、線膨張率が9.1×10-5/Kで厚さが0.2mmのオレフィン系樹脂フィルム(オレフィン系樹脂35質量部、金属水酸化物塩60質量部、層状珪酸塩5質量部からなる樹脂組成物のフィルム)を用いた以外は、実施例1と同様にして厚さ2.0mmの床材を得た。
<Example 6>
As a surface resin sheet, an olefin resin film having a linear expansion coefficient of 9.1 × 10 −5 / K and a thickness of 0.1 mm (35 parts by mass of olefin resin, 60 parts by mass of metal hydroxide salt, layered silicate) An olefin resin film having a linear expansion coefficient of 9.1 × 10 −5 / K and a thickness of 0.2 mm (35 mass of olefin resin) is used as the back resin sheet. A flooring material having a thickness of 2.0 mm was obtained in the same manner as in Example 1, except that a resin composition film comprising 5 parts by mass, metal hydroxide salt and 5 parts by mass of layered silicate was used.

<比較例1>
表面樹脂シートとして、線膨張率が10.9×10-5/Kで厚さが0.1mmのオレフィン系樹脂フィルム(オレフィン系樹脂50質量部、金属水酸化物塩45質量部、層状珪酸塩5質量部からなる樹脂組成物のフィルム)を用い、裏面樹脂シートとして、線膨張率が10.9×10-5/Kで厚さが0.2mmのオレフィン系樹脂フィルム(オレフィン系樹脂50質量部、金属水酸化物塩45質量部、層状珪酸塩5質量部からなる樹脂組成物のフィルム)を用いた以外は、実施例1と同様にして厚さ2.0mmの床材を得た。
<Comparative Example 1>
As a surface resin sheet, an olefin resin film having a linear expansion coefficient of 10.9 × 10 −5 / K and a thickness of 0.1 mm (50 parts by mass of olefin resin, 45 parts by mass of metal hydroxide salt, layered silicate) An olefin resin film having a linear expansion coefficient of 10.9 × 10 −5 / K and a thickness of 0.2 mm (50 mass of olefin resin) is used as the back resin sheet. A flooring material having a thickness of 2.0 mm was obtained in the same manner as in Example 1, except that a resin composition film consisting of 5 parts by mass, metal hydroxide salt and 5 parts by mass of layered silicate was used.

<比較例2>
表面樹脂シートとして、線膨張率が9.1×10-5/Kで厚さが0.1mmのオレフィン系樹脂フィルム(オレフィン系樹脂35質量部、金属水酸化物塩60質量部、層状珪酸塩5質量部からなる樹脂組成物のフィルム)を用い、裏面樹脂シートとして、線膨張率が10.9×10-5/Kで厚さが0.2mmのオレフィン系樹脂フィルム(オレフィン系樹脂50質量部、金属水酸化物塩45質量部、層状珪酸塩5質量部からなる樹脂組成物のフィルム)を用いた以外は、実施例1と同様にして厚さ2.0mmの床材を得た。
<Comparative example 2>
As a surface resin sheet, an olefin resin film having a linear expansion coefficient of 9.1 × 10 −5 / K and a thickness of 0.1 mm (35 parts by mass of olefin resin, 60 parts by mass of metal hydroxide salt, layered silicate) An olefin resin film having a linear expansion coefficient of 10.9 × 10 −5 / K and a thickness of 0.2 mm (50 mass of olefin resin) is used as the back resin sheet. A flooring material having a thickness of 2.0 mm was obtained in the same manner as in Example 1, except that a resin composition film consisting of 5 parts by mass, metal hydroxide salt and 5 parts by mass of layered silicate was used.

<比較例3>
表面樹脂層の厚さを0.01mm、裏面樹脂層の厚さを0.02mmに設定した以外は、実施例1と同様にして厚さ1.7mmの床材を得た。
<Comparative Example 3>
A flooring material having a thickness of 1.7 mm was obtained in the same manner as in Example 1 except that the thickness of the front surface resin layer was set to 0.01 mm and the thickness of the back surface resin layer was set to 0.02 mm.

<比較例4>
表面樹脂層の厚さを0.06mm、裏面樹脂層の厚さを0.6mmに設定し、裏面樹脂層の厚さ/表面樹脂層の厚さ=10.0に設定した以外は、実施例1と同様にして厚さ2.3mmの床材を得た。
<Comparative example 4>
Example except that the thickness of the surface resin layer was set to 0.06 mm, the thickness of the back surface resin layer was set to 0.6 mm, and the thickness of the back surface resin layer / the thickness of the surface resin layer was set to 10.0 In the same manner as in Example 1, a 2.3 mm thick flooring was obtained.

<比較例5>
表面樹脂層の厚さを0.2mm、裏面樹脂層の厚さを0.1mmに設定し、裏面樹脂層の厚さ/表面樹脂層の厚さ=0.5に設定した以外は、実施例1と同様にして厚さ2.0mmの床材を得た。
<Comparative Example 5>
Example except that the thickness of the surface resin layer was set to 0.2 mm, the thickness of the back surface resin layer was set to 0.1 mm, and the thickness of the back surface resin layer / the thickness of the surface resin layer was set to 0.5 In the same manner as in No. 1, a flooring material having a thickness of 2.0 mm was obtained.

<比較例6>
表面樹脂層の厚さを1.2mm、裏面樹脂層の厚さを1.2mmに設定した以外は、実施例1と同様にして厚さ4.0mmの床材を得た。
<Comparative Example 6>
A flooring having a thickness of 4.0 mm was obtained in the same manner as in Example 1 except that the thickness of the front surface resin layer was set to 1.2 mm and the thickness of the back surface resin layer was set to 1.2 mm.

なお、表面樹脂シートの線膨張率、裏面樹脂シートの線膨張率は、下記線膨張率測定法により測定された線膨張率(1/K)である。   In addition, the linear expansion coefficient of a surface resin sheet and the linear expansion coefficient of a back surface resin sheet are the linear expansion coefficients (1 / K) measured by the following linear expansion coefficient measuring method.

<線膨張率測定法>
セイコーインスツル社製の熱応力分析装置(TMA)「EXSTAR TMA/SS6000」を用い、JIS K7197−1991に準拠して、各シート(表面樹脂シート、裏面樹脂シート)の線膨張率(1/K)を測定する。この線膨張率の測定の際には、30℃〜60℃の条件下で線膨張量を測定し、この30℃〜60℃の範囲での線膨張量の測定データに基づいて線膨張率の平均値(30℃〜60℃の測定温度範囲での線膨張率の平均値)を算出するものとする。
<Linear expansion coefficient measurement method>
Using a thermal stress analyzer (TMA) “EXSTAR TMA / SS6000” manufactured by Seiko Instruments Inc., in accordance with JIS K7197-1991, the linear expansion coefficient (1 / K) of each sheet (surface resin sheet, back surface resin sheet) ). When measuring the linear expansion coefficient, the linear expansion amount is measured under the conditions of 30 ° C. to 60 ° C., and the linear expansion coefficient is measured based on the measurement data of the linear expansion amount in the range of 30 ° C. to 60 ° C. An average value (average value of linear expansion coefficient in a measurement temperature range of 30 ° C. to 60 ° C.) is calculated.

Figure 2013113022
Figure 2013113022

Figure 2013113022
Figure 2013113022

上記のようにして得られた各床材に対して、下記評価方法に基づいて評価を行った。これらの評価結果を表1、2に示す。   Each flooring obtained as described above was evaluated based on the following evaluation method. The evaluation results are shown in Tables 1 and 2.

<膨れ防止性評価法>
40cm×40cmの大きさの平面視正方形状に切り出した床材を、20℃雰囲気下で表面が平滑な木材製固定板の上にアクリル系接着剤で接着し、20℃雰囲気下で72時間放置した後、床材の4辺を金具で固定板に固定し、さらに60℃のオーブン内に4時間放置した。しかる後、オーブン内から床材を取り出し、床材の表面を目視観察し、膨れが全く生じていないものを「◎」、膨れがほんの僅かしか認められず実質的に膨れがないと判断できるものを「○」、膨れが少し生じたものを「△」、膨れが目立って生じたものを「×」とした。
<Swelling prevention evaluation method>
A flooring cut out in a square shape of 40 cm × 40 cm in plan view is bonded with an acrylic adhesive on a wood fixing plate having a smooth surface in an atmosphere at 20 ° C., and left for 72 hours in an atmosphere at 20 ° C. After that, the four sides of the flooring were fixed to the fixing plate with metal fittings, and further left in an oven at 60 ° C. for 4 hours. After that, take out the flooring from the oven, visually observe the surface of the flooring, "◎" if there is no blistering at all, it can be judged that there is only a slight blistering, and there is no substantial swelling Is indicated by “◯”, the case where the swelling slightly occurred is indicated by “△”, and the case where the swelling is conspicuous is indicated by “X”.

<反り防止性評価法>
JIS A1454−2010 14の反り試験に準拠して床材の反り量(mm)を測定し、下記判定基準に基づき評価した。
(判定基準)
「○」…反り量が−1.0mm以上0.0mm以下(例えば−0.5mm)
「△」…反り量が0.0mmを超えて0.5mm以下
「×」…反り量が0.5mmを超える、または反り量が−1.0mm未満(例えば−2.0mm)。
<Evaluation method for warpage prevention>
Based on the warpage test of JIS A1454-201014, the warpage amount (mm) of the flooring was measured and evaluated based on the following criteria.
(Criteria)
“◯”: warpage amount is −1.0 mm or more and 0.0 mm or less (for example, −0.5 mm)
“Δ”: The amount of warpage exceeds 0.0 mm to 0.5 mm or less. “X”: The amount of warpage exceeds 0.5 mm, or the amount of warpage is less than −1.0 mm (for example, −2.0 mm).

<施工性(硬さ)評価法>
JIS K7171−2008に準拠して床材の曲げ弾性率(MPa)を測定し、下記判定基準に基づき評価した。
(判定基準)
「◎」…曲げ弾性率が500MPa以下である
「○」…曲げ弾性率が500MPaを超えて700MPa以下である
「×」…曲げ弾性率が700MPaを超える。
<Evaluation method for workability (hardness)>
The flexural modulus (MPa) of the flooring was measured according to JIS K7171-2008 and evaluated based on the following criteria.
(Criteria)
“◎”: Bending elastic modulus is 500 MPa or less “◯”: Bending elastic modulus is over 500 MPa to 700 MPa or less “X”: Bending elastic modulus is over 700 MPa.

<突き上げ防止性評価法>
40cm×40cmの大きさの平面視正方形状に切り出した床材9枚を、縦3枚、横3枚ずつ碁盤目状に隙間なく整列配置した状態で、20℃雰囲気下で表面が平滑な木材製固定板の上にアクリル系接着剤で接着し、20℃雰囲気下で72時間放置した後、これら整列配置された9枚の床材の4辺(全体としての4辺)を金具で固定板に固定し、さらに60℃のオーブン内に4時間放置した。しかる後、オーブン内から床材を取り出し、隣り合う床材同士で突き上げが全く発生しなかったものを「◎」、隣り合う床材同士で突き上げがほんの僅かな程度認められたものの実用上問題がないと判断できるものを「○」、隣り合う床材同士で突き上げが少し発生したものを「△」、隣り合う床材同士で突き上げが目立って発生したものを「×」とした。
<Push-up prevention evaluation method>
Wood with a smooth surface in an atmosphere of 20 ° C. with 9 floors cut into a square shape of 40 cm × 40 cm in a plan view and arranged horizontally and 3 by 3 in a grid pattern without gaps After adhering on the fixed plate made of acrylic with an acrylic adhesive and leaving it in an atmosphere at 20 ° C. for 72 hours, fix the four sides (four sides as a whole) of the nine arranged flooring materials with metal fittings. And then left in an oven at 60 ° C. for 4 hours. After that, the floor material is taken out from the oven, and “(◎)” indicates that there was no push-up between adjacent floor materials. “◯” indicates that it could be determined that there was no thrust, “Δ” indicates that a slight push-up occurred between adjacent floor materials, and “x” indicates that a push-up occurred contiguously between adjacent floor materials.

表から明らかなように、本発明の実施例1〜6の床材は、膨れ防止性、反り防止性、施工性、施工後の突き上げ防止性のいずれにも優れていた。   As is clear from the table, the flooring materials of Examples 1 to 6 of the present invention were excellent in all of swelling prevention, warpage prevention, workability, and push-up prevention after construction.

これに対し、表面樹脂シート、裏面樹脂シートのうち少なくとも一方が、線膨張率が10.0×10-5/Kを超えている比較例1、2の床材は、膨れ防止性、突き上げ防止性のいずれにも劣っていた。また、表面樹脂層及び裏面樹脂層の厚さが本発明の規定範囲の下限を逸脱している比較例3の床材は、膨れ防止性、突き上げ防止性のいずれにも劣っていた。また、(裏面樹脂層の厚さ/表面樹脂層の厚さ)の比が、本発明の規定範囲を逸脱している比較例4、5の床材は、反り防止性に劣っていた。また、また、表面樹脂層及び裏面樹脂層の厚さが本発明の規定範囲の上限を逸脱している比較例6の床材は、柔軟性が不十分であり施工性に劣っていた。 On the other hand, the flooring material of Comparative Examples 1 and 2 in which at least one of the front surface resin sheet and the back surface resin sheet has a linear expansion coefficient exceeding 10.0 × 10 −5 / K has the swelling prevention property and the pushup prevention property. It was inferior to any sex. Moreover, the floor material of the comparative example 3 in which the thickness of the surface resin layer and the back surface resin layer deviates from the lower limit of the specified range of the present invention was inferior in both the swelling prevention property and the push-up prevention property. Moreover, the flooring of Comparative Examples 4 and 5 in which the ratio of (thickness of the back surface resin layer / thickness of the surface resin layer) deviated from the specified range of the present invention was inferior in warpage prevention properties. Moreover, the flooring of Comparative Example 6 in which the thicknesses of the front surface resin layer and the back surface resin layer deviate from the upper limit of the specified range of the present invention was insufficient in flexibility and inferior in workability.

本発明の床材は、例えば、ビル、マンション、家屋、商業施設等の建築物の床材、或いは鉄道、バス等の車輌の床材として好適に用いられるが、特にこのような用途に限定されるものではない。   The flooring of the present invention is suitably used, for example, as a flooring for buildings such as buildings, condominiums, houses, and commercial facilities, or a flooring for vehicles such as railways and buses, but is particularly limited to such applications. It is not something.

1…床材
2…表面樹脂層
3…中間樹脂層
4…裏面樹脂層
11…上側中間樹脂層
12…ガラス基布層
13…下側中間樹脂層
DESCRIPTION OF SYMBOLS 1 ... Flooring material 2 ... Surface resin layer 3 ... Intermediate resin layer 4 ... Back surface resin layer 11 ... Upper side intermediate resin layer 12 ... Glass base fabric layer 13 ... Lower side intermediate resin layer

Claims (5)

中間樹脂層の上面側に表面樹脂層が積層一体化され、前記中間樹脂層の下面側に裏面樹脂層が積層一体化されてなる床材であって、
前記表面樹脂層、前記中間樹脂層及び前記裏面樹脂層は、樹脂成分として、化学構造中に塩素原子を有しない樹脂のみが実質的に用いられてなる樹脂層であり、
前記表面樹脂層は、線膨張率が10.0×10-5/K以下である表面樹脂シートが前記中間樹脂層の上面側に積層されたものであり、
前記裏面樹脂層は、線膨張率が10.0×10-5/K以下である裏面樹脂シートが前記中間樹脂層の下面側に積層されたものであり、
前記表面樹脂層の厚さは0.03mm〜1.0mmであり、前記裏面樹脂層の厚さは0.03mm〜1.0mmであり、前記裏面樹脂層の厚さは、前記表面樹脂層の厚さの1.0倍〜4.0倍の範囲であることを特徴とする床材。
A floor material in which a surface resin layer is laminated and integrated on the upper surface side of the intermediate resin layer, and a back resin layer is laminated and integrated on the lower surface side of the intermediate resin layer,
The surface resin layer, the intermediate resin layer, and the back resin layer are resin layers in which only a resin having no chlorine atom in the chemical structure is substantially used as a resin component,
The surface resin layer is obtained by laminating a surface resin sheet having a linear expansion coefficient of 10.0 × 10 −5 / K or less on the upper surface side of the intermediate resin layer,
The back resin layer is obtained by laminating a back resin sheet having a linear expansion coefficient of 10.0 × 10 −5 / K or less on the lower surface side of the intermediate resin layer,
The thickness of the surface resin layer is 0.03 mm to 1.0 mm, the thickness of the back surface resin layer is 0.03 mm to 1.0 mm, and the thickness of the back surface resin layer is the thickness of the surface resin layer. A flooring material having a thickness in the range of 1.0 to 4.0 times the thickness.
前記表面樹脂層及び前記裏面樹脂層は、樹脂成分の主成分として、非晶性ポリエステル樹脂が用いられている請求項1に記載の床材。   The flooring material according to claim 1, wherein the front surface resin layer and the back surface resin layer use an amorphous polyester resin as a main component of a resin component. 前記中間樹脂層は、ガラス基布層と、該ガラス基布層の上面側に積層された上側中間樹脂層と、前記ガラス基布層の下面側に積層された下側中間樹脂層と、を含み、
前記上側中間樹脂層及び前記下側中間樹脂層は、樹脂成分として、化学構造中に塩素原子を有しない樹脂のみが実質的に用いられてなる樹脂層であることを特徴とする請求項1または2に記載の床材。
The intermediate resin layer includes a glass base fabric layer, an upper intermediate resin layer laminated on the upper surface side of the glass base fabric layer, and a lower intermediate resin layer laminated on the lower surface side of the glass base fabric layer. Including
2. The upper intermediate resin layer and the lower intermediate resin layer are resin layers in which only a resin having no chlorine atom in a chemical structure is substantially used as a resin component. The flooring according to 2.
前記上側中間樹脂層及び前記下側中間樹脂層は、樹脂成分として、ポリプロピレン系エラストマー及びポリプロピレン系樹脂が用いられている請求項3に記載の床材。   The floor material according to claim 3, wherein the upper intermediate resin layer and the lower intermediate resin layer are made of polypropylene elastomer and polypropylene resin as resin components. 前記表面樹脂層の下面に印刷層が形成され、該印刷層の下面にカルボン酸変性ポリオレフィン樹脂を含有してなるプライマー塗布層が形成されている請求項1〜4のいずれか1項に記載の床材。   The printing layer is formed in the lower surface of the said surface resin layer, The primer coating layer containing a carboxylic acid modified polyolefin resin is formed in the lower surface of this printing layer. Flooring.
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2015148083A (en) * 2014-02-06 2015-08-20 東リ株式会社 Floor material
JP2016223154A (en) * 2015-05-29 2016-12-28 住江織物株式会社 Floor material with excellent shapability
KR101755075B1 (en) * 2014-06-30 2017-07-07 (주)엘지하우시스 decorative flooring using composite high pressure laminate

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006052601A (en) * 2004-08-13 2006-02-23 Ryoichi Kitamura Tile material
JP2006281657A (en) * 2005-04-01 2006-10-19 Sekisui Chem Co Ltd Laminated molded product
JP2010059611A (en) * 2008-09-01 2010-03-18 Suminoe Textile Co Ltd Olefinic floor material

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006052601A (en) * 2004-08-13 2006-02-23 Ryoichi Kitamura Tile material
JP2006281657A (en) * 2005-04-01 2006-10-19 Sekisui Chem Co Ltd Laminated molded product
JP2010059611A (en) * 2008-09-01 2010-03-18 Suminoe Textile Co Ltd Olefinic floor material

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2015148083A (en) * 2014-02-06 2015-08-20 東リ株式会社 Floor material
KR101755075B1 (en) * 2014-06-30 2017-07-07 (주)엘지하우시스 decorative flooring using composite high pressure laminate
JP2016223154A (en) * 2015-05-29 2016-12-28 住江織物株式会社 Floor material with excellent shapability

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