Deprecated: The each() function is deprecated. This message will be suppressed on further calls in /home/zhenxiangba/zhenxiangba.com/public_html/phproxy-improved-master/index.php on line 456
JP5486283B2 - Base material for foamed resin laminate sheet - Google Patents
[go: Go Back, main page]

JP5486283B2 - Base material for foamed resin laminate sheet - Google Patents

Base material for foamed resin laminate sheet Download PDF

Info

Publication number
JP5486283B2
JP5486283B2 JP2009278651A JP2009278651A JP5486283B2 JP 5486283 B2 JP5486283 B2 JP 5486283B2 JP 2009278651 A JP2009278651 A JP 2009278651A JP 2009278651 A JP2009278651 A JP 2009278651A JP 5486283 B2 JP5486283 B2 JP 5486283B2
Authority
JP
Japan
Prior art keywords
base material
layer
foamed resin
fibers
resin
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.)
Active
Application number
JP2009278651A
Other languages
Japanese (ja)
Other versions
JP2011121192A (en
Inventor
真規子 橋本
智之 高崎
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Asahi Kasei Corp
Original Assignee
Asahi Kasei Fibers Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Asahi Kasei Fibers Corp filed Critical Asahi Kasei Fibers Corp
Priority to JP2009278651A priority Critical patent/JP5486283B2/en
Publication of JP2011121192A publication Critical patent/JP2011121192A/en
Application granted granted Critical
Publication of JP5486283B2 publication Critical patent/JP5486283B2/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Laminated Bodies (AREA)

Description

本発明は、例えば壁材、天井材、床材等の建築物内装材として使用される、合成樹脂発泡層を有する発泡樹脂積層シートにおいて、基材として使用できる発泡樹脂積層シート用基材に関するものである。   The present invention relates to a base material for a foamed resin laminate sheet that can be used as a base material in a foamed resin laminate sheet having a synthetic resin foam layer, for example, used as a building interior material such as a wall material, a ceiling material, and a flooring material. It is.

従来、建築用内装材としては、グラビアプリント、ロータリースクリーンプリント等の意匠表現が容易にでき、耐久性に優れ、かつ汚れ等の除去も容易に行うことのできる、塩化ビニル系樹脂等で形成された合成樹脂製の内装材が主流を占めている。このような内装材は、飲食店等の店舗や集合住宅等において持ち主の変更に伴う改装等により張り替えられる。   Conventionally, as an interior material for construction, it is formed of a vinyl chloride resin or the like that can easily express a design such as gravure printing, rotary screen printing, etc., has excellent durability, and can easily remove dirt and the like. Synthetic resin interior materials are the mainstream. Such interior materials are replaced by refurbishment or the like in accordance with the change of owner in stores such as restaurants and apartment houses.

このような合成樹脂製の内装材では、通常紙基材が裏打材として使用されており、澱粉糊等の接着剤を介して壁の基体となる石膏ボード等に貼付けられる。しかしながら、改装の際、紙基材が裏打材として使用された内装材を剥がそうとすると、紙基材が破れやすく剥がす手間がかかるという問題点を有していた。このような問題点を解決するため、例えば特許文献1、特許文献2及び特許文献3のように、これまでは発泡樹脂積層シートの構成、紙基材に被覆層を設けること等、より層間剥離性を向上させる検討が行われてきた。   In such an interior material made of a synthetic resin, a paper base is usually used as a backing material, and is attached to a gypsum board or the like serving as a wall substrate through an adhesive such as starch paste. However, when refurbishing, if the paper base material is to be peeled off the interior material used as a backing material, there is a problem that the paper base material is easily broken and takes time and effort. In order to solve such problems, for example, Patent Document 1, Patent Document 2 and Patent Document 3, so far, the configuration of the foamed resin laminated sheet, the provision of a coating layer on the paper substrate, etc., more delamination Consideration has been made to improve performance.

特許文献4には、特定の樹脂の基材としてポリエステル不織布が挙げられている。しかしながら、該基材の具体的な内容は示されていない。   Patent Document 4 mentions a polyester nonwoven fabric as a base material of a specific resin. However, the specific content of the substrate is not shown.

特許第3283639号公報Japanese Patent No. 3283639 特許第2891760号公報Japanese Patent No. 2891760 特許第3144777号公報Japanese Patent No. 3144777 特許第3949797号公報Japanese Patent No. 3949797

従って、剥がしやすさという機能が得られるように基材が満足すべき特定の条件については従来考慮されていない。また、層間剥離性を改良すると、改装時の剥がしやすさは向上するものの、施工時及び使用中に接触等の衝撃が加わった際により剥がれやすくなり施工時の取り扱いが難しく、耐久性が短くなる等の問題が生じていた。更に、基材又は裏打材として紙を用いる場合、紙が長期使用において吸放湿することにより寸法変化を起こして目地に隙間が開くという問題があった。   Therefore, the specific conditions that the base material should satisfy so as to obtain the function of ease of peeling have not been conventionally considered. In addition, improving delamination improves the ease of peeling during refurbishment, but makes it easier to peel off when subjected to impacts such as contact during construction and use, making handling difficult during construction and shortening durability Etc. had occurred. Further, when paper is used as a base material or backing material, there is a problem that a dimensional change occurs due to moisture absorption / release in the long-term use, and a gap is formed in the joint.

本発明の課題は、発泡樹脂層との密着性に優れ、基材が緻密化されているために強度が高く、繊維が脱落しにくい構造を有しているため剥がしやすく、加工性(すなわち合成樹脂塗工時の裏抜け防止性、並びに乾燥工程時及び発泡工程時の熱による寸法安定性)に優れ、さらに施工後の寸法安定性にも優れた発泡樹脂積層シート用基材を提供することにある。   The object of the present invention is to provide excellent adhesion to the foamed resin layer, high strength because the base material is densified, and a structure in which fibers are difficult to fall off, and is easy to peel off. To provide a base material for a foamed resin laminate sheet that is excellent in prevention of see-through during resin coating and dimensional stability due to heat during the drying process and foaming process, and also excellent in dimensional stability after construction. It is in.

本発明者は、所定の条件を満足するポリエステル系不織布を発泡樹脂積層シートの基材として使用することにより、改装の際破れることなく剥がすことができるとともに施工後の環境変化による寸法変化が少ない発泡樹脂積層シートが得られることを見出し、本発明に到達した。すなわち本発明は以下の通りである。
[1] 基材と該基材上に形成された発泡樹脂層とを有する発泡樹脂積層シートを形成するために用いる該基材であって、
ポリエステル系繊維を主成分とする見かけ密度0.3〜0.9g/cm3の不織布であり、発泡樹脂層の形成面となる表面の凹凸度が、1〜30μmであり、
該基材は、該発泡樹脂層の形成面を与える表面層、該表面層に接する中間層及び該中間層に接する裏面層が熱圧着により一体化されている積層不織布であり、かつ下記(1)〜(3):
(1)表面層が、繊維径7〜30μmの熱可塑性樹脂長繊維からなる層を少なくとも1層有すること、
(2)中間層が、繊維径1〜5μmのメルトブロウン繊維からなる層を少なくとも1層有し、目付が1g/m 2 以上であり、かつ積層不織布の目付の30質量%以下を構成すること、及び
(3)裏面層が、繊維径7〜30μmの熱可塑性樹脂長繊維からなる層を少なくとも1層有し、かつ目付が3〜40g/m 2 であること
を満足する、発泡樹脂積層シート用基材。
[2] 繊維径1〜30μmの繊維からなり、目付が30〜100g/m2であり、かつ厚みが35〜300μmである、上記[1]に記載の発泡樹脂積層シート用基材。
[3] 180℃環境下無張力で3分間保持したときの乾熱寸法変化率が、経方向0%〜−5.0%、緯方向−1.0%〜3.0%である、上記[1]又は[2]に記載の発泡樹脂積層シート用基材。
[4] レンダー処理されている、上記[1]〜[]のいずれかに記載の発泡樹脂積層シート用基材。
The present inventor uses a polyester-based nonwoven fabric satisfying predetermined conditions as a base material of the foamed resin laminated sheet, and can be peeled without tearing during refurbishment, and foaming with little dimensional change due to environmental changes after construction. The present inventors have found that a resin laminated sheet can be obtained and have reached the present invention. That is, the present invention is as follows.
[1] The base material used for forming a foamed resin laminate sheet having a base material and a foamed resin layer formed on the base material,
A nonwoven fabric apparent density 0.3-0.9 g / cm 3 composed mainly of polyester fibers, irregularities of the surface to be formed surface of the foamed resin layer, Ri. 1 to 30 [mu] m der,
The base material is a laminated non-woven fabric in which a surface layer that provides a surface for forming the foamed resin layer, an intermediate layer in contact with the surface layer, and a back surface layer in contact with the intermediate layer are integrated by thermocompression bonding, and the following (1 ) To (3):
(1) The surface layer has at least one layer of thermoplastic resin long fibers having a fiber diameter of 7 to 30 μm,
(2) The intermediate layer has at least one layer composed of melt-blown fibers having a fiber diameter of 1 to 5 μm, has a basis weight of 1 g / m 2 or more, and constitutes 30% by mass or less of the basis weight of the laminated nonwoven fabric. ,as well as
(3) the back surface layer, a layer made of thermoplastic resin long fibers having a fiber diameter of 7~30μm having at least one layer, and the basis weight is 3~40g / m 2
A base material for a foamed resin laminated sheet that satisfies the requirements.
[2] The base material for a foamed resin laminated sheet according to the above [1], comprising fibers having a fiber diameter of 1 to 30 μm, a basis weight of 30 to 100 g / m 2 , and a thickness of 35 to 300 μm.
[3] The dimensional change rate of dry heat when held for 3 minutes under no tension in an environment of 180 ° C. is 0% to −5.0% in the warp direction and −1.0% to 3.0% in the weft direction. The base material for foamed resin laminated sheets according to [1] or [2].
[4] mosquitoes are rendered processed, the above-mentioned [1] to [3] foamed resin laminate sheet for a substrate according to any one of.

本発明の発泡樹脂積層シート用基材は、加工性が良好で、発泡樹脂層を直接コーティング等により形成できるものであり、例えば紙基材等の裏打なしで、基材と発泡樹脂との密着性が良好な発泡樹脂積層シートを形成できる。すなわち、基材の見かけ密度を所定の範囲にコントロールすることにより、発泡樹脂が基材に適度にしみこみ密着して一体化し、基材が緻密化することにより繊維同士が強固に圧着され、はがれにくく、繊維くずが出にくいとともに強度が高くなる。このため、本発明の発泡樹脂積層シート用基材は強度に優れ、これを用いて形成される発泡樹脂積層シートは、例えば壁の基体となる石膏ボード等に貼り付けることができ、改装の際は、例えば紙基材を用いる場合のように破れることなく剥がすのが容易である。更に、本発明の発泡樹脂積層シート用基材は環境変化による寸法変化が少なく、施工後長期間経過しても目地が開く等の問題が生じにくいという利点を有する。   The base material for the foamed resin laminate sheet of the present invention has good processability and can form the foamed resin layer directly by coating or the like. For example, adhesion between the base material and the foamed resin without backing of a paper base material or the like. A foamed resin laminate sheet with good properties can be formed. In other words, by controlling the apparent density of the base material within a predetermined range, the foamed resin is appropriately infiltrated and closely integrated with the base material, and when the base material is densified, the fibers are firmly pressed together and difficult to peel off. , Fiber scraps are hard to come out and strength is increased. For this reason, the base material for foamed resin laminate sheets of the present invention is excellent in strength, and the foamed resin laminate sheet formed using the base material can be affixed to, for example, a gypsum board as a base of a wall. Can be easily peeled off without tearing, such as when using a paper substrate. Furthermore, the base material for a foamed resin laminated sheet of the present invention has the advantage that there is little dimensional change due to environmental changes, and problems such as opening of joints are unlikely to occur even after a long period after construction.

以下、本発明について詳細に説明する。   Hereinafter, the present invention will be described in detail.

[発泡樹脂積層シート用基材]
本発明の一態様は、基材と該基材上に形成された発泡樹脂層とを有する発泡樹脂積層シートを形成するために用いる該基材であって、ポリエステル系繊維を主成分とする見かけ密度0.3〜0.9g/cm3の不織布であり、発泡樹脂層形成面となる表面の凹凸度が1〜150μmである、発泡樹脂積層シート用基材を提供する。本発明の発泡樹脂積層シート用基材(以下、基材ということもある)は、例えば建築内装材の装飾層等となる発泡樹脂層の形成のための基材として用いられ、該発泡樹脂層とともに発泡樹脂積層シート(以下、積層シートということもある)を形成できるものである。なお発泡樹脂層の詳細については後述する。本発明の発泡樹脂積層シート用基材としては、1層の不織布、又は1層以上の不織布層を含む複数の層からなる積層不織布を用いることができる。
[Base material for foamed resin laminate sheet]
One aspect of the present invention is a base material used for forming a foamed resin laminate sheet having a base material and a foamed resin layer formed on the base material, and is an appearance mainly composed of polyester fibers Provided is a base material for a foamed resin laminate sheet, which is a nonwoven fabric having a density of 0.3 to 0.9 g / cm 3 , and has a surface irregularity degree of 1 to 150 μm serving as a foamed resin layer forming surface. The base material for a foamed resin laminate sheet of the present invention (hereinafter sometimes referred to as a base material) is used as a base material for forming a foamed resin layer that serves as a decorative layer of a building interior material, for example. At the same time, a foamed resin laminated sheet (hereinafter sometimes referred to as a laminated sheet) can be formed. Details of the foamed resin layer will be described later. As the base material for the foamed resin laminated sheet of the present invention, a single layer nonwoven fabric or a laminated nonwoven fabric composed of a plurality of layers including one or more nonwoven fabric layers can be used.

本発明の発泡樹脂積層シート用基材は、ポリエステル系繊維を主成分とする不織布である。本明細書において、ポリエステル系繊維を主成分とする不織布とは、不織布を構成する要素のうちポリエステル系繊維の含有量(質量基準)が最も多い不織布を意味するが、特に典型的には、不織布の少なくとも70質量%をポリエステル系繊維が占めている不織布である。本発明の発泡樹脂積層シート用基材は、ポリエステル系繊維を主成分とすることによって、例えば従来の紙基材と比べて、破断強度が高く、環境条件下での長期使用時の寸法変化が少ない。よって本発明の発泡樹脂積層シート用基材を用いることにより、強度が高く剥がしやすいため施工時の取り扱い性が良好で、かつ施工後の寸法安定性が良好な発泡樹脂積層シートを得ることができる。   The base material for foamed resin laminated sheets of the present invention is a nonwoven fabric mainly composed of polyester fibers. In the present specification, the nonwoven fabric mainly composed of polyester fibers means a nonwoven fabric having the largest content (mass basis) of polyester fibers among the elements constituting the nonwoven fabric. It is a nonwoven fabric in which at least 70% by mass of polyester fiber occupies. The base material for the foamed resin laminate sheet of the present invention has a high breaking strength and, for example, a dimensional change during long-term use under environmental conditions by using polyester fiber as a main component, for example, compared to a conventional paper base material. Few. Therefore, by using the base material for the foamed resin laminate sheet of the present invention, it is possible to obtain a foamed resin laminate sheet that has high strength and is easy to peel off, has good handleability during construction, and good dimensional stability after construction. .

ポリエステル系繊維は、ポリエチレンテレフタレート(PET)、ポリブチレンテレフタレート(PBT)、及びポリトリメチレンテレフタレート(PTT)等のポリエステル単独重合体、ポリエステル系共重合体、単独重合体と共重合体との混合物等から形成できる。ポリエステル系共重合体としては、テレフタル酸、イソフタル酸、フタル酸、ナフタリンジカルボン酸等の芳香族ジカルボン酸と、エチレングリコール、ジエチレングリコール、1,4−ブタンジオール、シクロヘキサンジメタノール等のジオールとが重合されたもの等が挙げられる。また、生分解性を有する樹脂、例えば、ポリ乳酸をはじめとする脂肪族ポリエステル樹脂を用いてもよい。さらに、例えばリン系有機モノマー等を共重合したポリマーを混用し難燃性を付与することもできる。ポリエステル系繊維としては、短繊維又は長繊維を単独で用いてもよく、2種以上の繊維を積層又は混合して用いてもよい。中でも、ポリエチレンテレフタレートで形成された長繊維不織布は耐熱性、強度の観点から好ましい。また、ポリエステル系繊維中に、他の成分として顔料、艶消し剤、酸化防止剤、紫外線吸収剤、難燃剤、鎖伸張剤等の各種添加剤を例えば10質量%未満混合しても差し支えない。   Polyester fibers are polyester homopolymers such as polyethylene terephthalate (PET), polybutylene terephthalate (PBT), and polytrimethylene terephthalate (PTT), polyester copolymers, mixtures of homopolymers and copolymers, etc. Can be formed from As polyester-based copolymers, aromatic dicarboxylic acids such as terephthalic acid, isophthalic acid, phthalic acid, and naphthalene dicarboxylic acid and diols such as ethylene glycol, diethylene glycol, 1,4-butanediol, and cyclohexanedimethanol are polymerized. And the like. Moreover, you may use biodegradable resin, for example, aliphatic polyester resin including polylactic acid. Further, for example, a polymer obtained by copolymerizing a phosphorus organic monomer or the like can be used in combination to impart flame retardancy. As the polyester fiber, short fibers or long fibers may be used alone, or two or more kinds of fibers may be laminated or mixed. Among these, a long fiber nonwoven fabric formed of polyethylene terephthalate is preferable from the viewpoint of heat resistance and strength. In addition, various additives such as pigments, matting agents, antioxidants, ultraviolet absorbers, flame retardants, and chain extenders may be mixed as less than 10% by mass in the polyester fiber.

ポリエステル系繊維の断面形状としては、丸型断面、並びに扁平型及びT型等の異形断面等が挙げられる。   Examples of the cross-sectional shape of the polyester fiber include a round cross-section, and irregular cross-sections such as a flat type and a T type.

ポリエステル系繊維を主成分とする不織布は、ポリエステル系繊維以外に、バインダー繊維、接着性樹脂等を30質量%以下で含有できる。   The nonwoven fabric which has a polyester fiber as a main component can contain a binder fiber, an adhesive resin, etc. in 30 mass% or less other than a polyester fiber.

バインダー繊維としては、公知の未延伸PET繊維、低融点ポリエステル繊維のようなポリエステル系繊維が挙げられる。また、例えば、実用的な強度に影響のない範囲において、少量のポリオレフィン等の低融点成分をポリエステル系繊維に加えて、不織布の可撓性を改質することもできる。また他の改質としては、ポリエステル系繊維を芯にポリオレフィン等を鞘に用いた芯鞘繊維とすること等が挙げられる。ポリエステル系繊維以外のバインダー繊維の不織布中の含有量としては、繊維同士の接着強度を強固にする観点から3質量%以上が好ましく、30質量%以下が好ましい。該含有量は、より好ましくは5〜20質量%である。   Examples of the binder fiber include known unstretched PET fibers and polyester fibers such as low melting point polyester fibers. In addition, for example, in a range that does not affect the practical strength, a low-melting-point component such as polyolefin can be added to the polyester fiber to modify the flexibility of the nonwoven fabric. Other modifications include a core-sheath fiber using a polyester fiber as a core and a polyolefin or the like as a sheath. As content in the nonwoven fabric of binder fibers other than a polyester fiber, 3 mass% or more is preferable and 30 mass% or less is preferable from a viewpoint of strengthening the adhesive strength of fibers. The content is more preferably 5 to 20% by mass.

接着性樹脂の使用は、ポリエステル系繊維として短繊維を使用する場合に特に有用であり、不織布に優れた形態保持性を与えることができる。接着性樹脂としては、アクリル樹脂、フェノール樹脂、ポリエステル樹脂、ポリビニルアルコール樹脂、ポリ塩化ビニル樹脂、並びにこれらの変性体及び混合体等からなる熱可塑性樹脂等を用いることができる。接着性樹脂の不織布中の含有量としては、繊維同士の接着強度を強固にする観点から3質量%以上が好ましく、ポリエステル系繊維を70質量%以上含有させる観点から30質量%以下が好ましい。該含有量は、より好ましくは5〜20質量%である。   The use of the adhesive resin is particularly useful when short fibers are used as the polyester fibers, and can give excellent shape retention to the nonwoven fabric. As the adhesive resin, an acrylic resin, a phenol resin, a polyester resin, a polyvinyl alcohol resin, a polyvinyl chloride resin, a thermoplastic resin made of a modified body or a mixture thereof, or the like can be used. As content in the nonwoven fabric of adhesive resin, 3 mass% or more is preferable from a viewpoint of strengthening the adhesive strength of fibers, and 30 mass% or less is preferable from a viewpoint of containing 70 mass% or more of polyester fiber. The content is more preferably 5 to 20% by mass.

本発明の発泡樹脂積層シート用基材は見かけ密度が0.3〜0.9g/cm3であることが必要である。発泡樹脂積層シート用基材は見かけ密度を0.3〜0.9g/cm3にすることにより適度に発泡性樹脂が基材中に浸透し、基材と発泡樹脂層との密着性が優れ、基材が緻密化され繊維間の接着性がよいために強度が高く、繊維が脱落しにくい構造になる。それ故、剥がしやすく、同時に加工性(すなわち合成樹脂塗工時の裏抜け防止性、並びに乾燥工程時及び発泡工程時の熱による寸法安定性)にも優れる基材が得られる。見かけ密度が0.3g/cm3未満であると、発泡樹脂層形成時に樹脂の裏抜けがしやすくなり、樹脂の塗工工程での加工性が悪くなるため好ましくない。また、見かけ密度が0.9g/cm3を超えると、不織布の密度が大きくなりすぎて、基材上にコーティング等によって発泡樹脂層を形成する際に発泡性合成樹脂組成物が進入すべき空隙が少なくなるため、発泡樹脂と基材との密着性が不十分となり好ましくない。基材と発泡性樹脂との密着性は発泡性樹脂の粘度を調整することによっても調整できる。粘度を低くすれば密着性はよくなるが裏抜けしやすくなり、粘度を高くすれば密着性が低下する傾向がある。見かけ密度を0.4〜0.9g/cm3に調整すれば通常使用される任意の樹脂を使用しても裏抜けすることなく問題なく使用でき好ましい。より好ましくは0.5〜0.8g/cm3である。上記見かけ密度は、後述の方法で測定される目付及び厚みから、式:見かけ密度=(目付)/(厚み)に従って算出される。 The apparent density of the base material for a foamed resin laminate sheet of the present invention is required to be 0.3 to 0.9 g / cm 3 . The base material for the foamed resin laminate sheet has an apparent density of 0.3 to 0.9 g / cm 3 , so that the foamable resin permeates the base material appropriately, and the adhesion between the base material and the foamed resin layer is excellent. Since the base material is densified and the adhesiveness between the fibers is good, the structure is strong and the fibers are difficult to fall off. Therefore, it is easy to peel off, and at the same time, a substrate having excellent processability (that is, prevention of see-through at the time of synthetic resin coating and dimensional stability due to heat at the time of the drying process and the foaming process) can be obtained. When the apparent density is less than 0.3 g / cm 3 , it is not preferable because the resin can be easily exposed when the foamed resin layer is formed, and the processability in the resin coating process is deteriorated. Further, when the apparent density exceeds 0.9 g / cm 3 , the density of the nonwoven fabric becomes too high, and voids into which the foamable synthetic resin composition should enter when forming the foamed resin layer on the substrate by coating or the like Therefore, the adhesiveness between the foamed resin and the substrate becomes insufficient, which is not preferable. The adhesion between the substrate and the expandable resin can be adjusted by adjusting the viscosity of the expandable resin. If the viscosity is lowered, the adhesion is improved, but it is easy to see through, and if the viscosity is increased, the adhesion tends to be lowered. If the apparent density is adjusted to 0.4 to 0.9 g / cm 3 , it can be used without any problem even if any commonly used resin is used, which is preferable. More preferably, it is 0.5 to 0.8 g / cm 3 . The apparent density is calculated according to the formula: apparent density = (weight per unit area) / (thickness) from the basis weight and thickness measured by the method described later.

本発明の発泡樹脂積層シート用基材は、基材の凹凸が発泡樹脂塗工時に発泡樹脂層の厚み斑につながり、発泡樹脂の発泡後に表面が凹凸になり、意匠性、柄付け性に影響を与える。それ故、基材は平滑であるほど好ましい。シート用基材においては、発泡樹脂層の形成面(例えばコーティング面)となる表面の凹凸度が、1〜150μmの範囲であれば意匠性を確保できる。表面の凹凸度が1μm未満である場合、発泡樹脂層と基材との密着性が低く、150μmを超える場合、発泡樹脂の形成(例えばコーティング)時に基材表面の凹部に厚く付着した発泡樹脂が発泡時に浮き上がるため、樹脂表面の平滑性の理由で内装材等の柄が制限される。上記凹凸度としては、1〜100μmが好ましく、1〜30μmが更に好ましい。上記凹凸度が1〜30μmの範囲である場合、発泡樹脂層の厚み及び柄に影響されず特に有利に使用できる。上記の表面の凹凸度は、非接触高速3次元形状システム(例えばコスム社製 非接触高速3次元形状システム MAP―3D)を使用し、発泡樹脂層形成面となる基材表面を上になるようスライドガラスに両面テープで固定し、20mm間を100μmピッチで表面凹凸を測定し、隣り合う山と谷間の高さを20個測定し数平均することによって求めることができる。特定の周期で凹凸を繰り返す柄(例えばエンボス)が存在する場合には、柄の凹凸の山谷間の高さを測定する。経緯20mm×20mm間をそれぞれ100μmピッチで測定したときに経方向と緯方向とで測定値が異なる場合、上記凹凸度は、より凹凸度が大きい方向での値を意味するものとする。   The base material for the foamed resin laminate sheet of the present invention has unevenness of the base material resulting in uneven thickness of the foamed resin layer when the foamed resin is applied, and the surface becomes uneven after foaming of the foamed resin, affecting the design and patterning properties. give. Therefore, it is preferable that the substrate is smooth. In the base material for sheet | seat, if the unevenness | corrugation degree of the surface used as the formation surface (for example, coating surface) of a foamed resin layer is the range of 1-150 micrometers, designability is securable. When the unevenness of the surface is less than 1 μm, the adhesion between the foamed resin layer and the substrate is low, and when it exceeds 150 μm, the foamed resin that is thickly attached to the recesses on the surface of the substrate during the formation of the foamed resin (for example, coating) Since it floats when foaming, the pattern of the interior material or the like is limited due to the smoothness of the resin surface. As said unevenness degree, 1-100 micrometers is preferable and 1-30 micrometers is still more preferable. When the unevenness is in the range of 1 to 30 μm, it can be used particularly advantageously without being influenced by the thickness and pattern of the foamed resin layer. The degree of unevenness of the above surface is determined so that the surface of the base material to be the foamed resin layer forming surface is up using a non-contact high-speed three-dimensional shape system (for example, non-contact high-speed three-dimensional shape system MAP-3D manufactured by Cosm) It can be obtained by fixing to a slide glass with double-sided tape, measuring surface irregularities at a pitch of 100 μm between 20 mm, measuring 20 heights between adjacent peaks and valleys, and averaging the numbers. When there is a pattern (for example, embossing) that repeats unevenness at a specific period, the height between peaks and valleys of the unevenness of the pattern is measured. If the measured values are different between the warp direction and the weft direction when measuring a distance of 20 mm × 20 mm at a pitch of 100 μm, the degree of unevenness means a value in a direction where the degree of unevenness is larger.

本発明の発泡樹脂積層シート用基材は、繊維径1〜30μmの繊維からなることが好ましい。該基材は、平均繊維径が好ましくは7〜30μmの単層不織布で形成できるが、この場合、平均繊維径1〜5μmの極細繊維を混在させるか又は積層することにより、より緻密化されやすく好ましい。繊維径が1μm未満の場合、基材の生産性が低下する傾向がある。また、繊維径が30μmを超える場合、表面の平滑性が低下するとともに発泡性合成樹脂の裏抜け防止性が低下する傾向がある。上記繊維径は、裏抜け防止性を高めるメルトブロウン層を形成するのに適正な範囲は1〜5μmであり、長繊維不織布、短繊維不織布を形成するのに好ましい範囲は7〜30μmである。上記繊維径は、マイクロスコープにより繊維の直径(異型断面の場合には外接円の直径)を測定したときの、例えば30点の数平均値として算出される値である。   The base material for a foamed resin laminate sheet of the present invention is preferably made of fibers having a fiber diameter of 1 to 30 μm. The base material can be formed of a single-layer nonwoven fabric having an average fiber diameter of preferably 7 to 30 μm, but in this case, it is more easily densified by mixing or laminating ultrafine fibers having an average fiber diameter of 1 to 5 μm. preferable. When the fiber diameter is less than 1 μm, the productivity of the substrate tends to decrease. On the other hand, when the fiber diameter exceeds 30 μm, the smoothness of the surface is lowered and the back-through preventing property of the foamable synthetic resin tends to be lowered. The fiber diameter is appropriately 1 to 5 μm for forming a meltblown layer that enhances the prevention of breakthrough, and preferably 7 to 30 μm for forming long fiber nonwoven fabrics and short fiber nonwoven fabrics. The fiber diameter is a value calculated, for example, as a number average value of 30 points when the diameter of the fiber (diameter of circumscribed circle in the case of an irregular cross section) is measured with a microscope.

本発明の発泡樹脂積層シート用基材の目付は30〜100g/m2であることが好ましい。目付が30g/m2未満の場合、発泡樹脂形成時に樹脂が裏抜けしやすくなる傾向がある。また、目付が100g/m2を超える場合、発泡樹脂積層シートを内装材等として用いる場合に、発泡樹脂積層シート自体の単位面積当たりの重量が増加し、施工性が低下する傾向がある。目付は、より好ましくは40〜80g/m2である。上記目付は、JIS−L−1906に準拠して求めることができる。 It is preferable that the fabric weight of the base material for foamed resin laminate sheets of the present invention is 30 to 100 g / m 2 . When the basis weight is less than 30 g / m 2 , the resin tends to be easily exposed when forming the foamed resin. Moreover, when a fabric weight exceeds 100 g / m < 2 >, when using a foamed resin laminated sheet as an interior material etc., there exists a tendency for the weight per unit area of foamed resin laminated sheet itself to increase, and for workability to fall. The basis weight is more preferably 40 to 80 g / m 2 . The basis weight can be determined in accordance with JIS-L-1906.

本発明の発泡樹脂積層シート用基材の厚みは35〜300μmであることが好ましい。厚みが35μm未満の場合は、見かけ密度を高くしても樹脂の裏抜け防止性が低い傾向がある。また厚みが300μmを超える場合は、基材が厚くなりすぎ、壁面角部の施工性が低下する傾向がある。厚みは、より好ましくは45〜200μm、更に好ましくは45〜110μm、特に好ましくは60〜100μmの範囲である。上記厚みは、厚み計(例えばPEACOCK製No.207)を用い、JIS−L−1906に準拠して求めることができる。   The thickness of the base material for a foamed resin laminate sheet of the present invention is preferably 35 to 300 μm. When the thickness is less than 35 μm, even if the apparent density is increased, there is a tendency for the resin to prevent back-through. Moreover, when thickness exceeds 300 micrometers, a base material becomes thick too much and there exists a tendency for the workability of a wall surface corner part to fall. The thickness is more preferably in the range of 45 to 200 μm, still more preferably 45 to 110 μm, particularly preferably 60 to 100 μm. The said thickness can be calculated | required based on JIS-L-1906 using a thickness meter (for example, No.207 by PEACOCK).

本発明の発泡樹脂積層シート用基材をスパンボンド法で製造し、エンボスロールで部分熱圧着する場合には、エンボス深さの小さい柄を用いることが基材の平滑性の観点でより好ましい。例えばエンボス深さは1mm以下が好ましく、0.5mm以下が更に好ましい。また、より平滑性を向上させるにはさらにカレンダー加工を施すことが好ましい。カレンダー加工により見かけ密度も向上させることができる。エンボスロール面ではなく、フラットロール面を発泡樹脂層の形成面とすることにより、エンボスロール面に発泡樹脂層を形成するのと比べてより平滑に樹脂を発泡させることができる。   When the base material for foamed resin laminate sheets of the present invention is produced by the spunbond method and partially thermocompression bonded with an embossing roll, it is more preferable from the viewpoint of the smoothness of the base material to use a handle with a small embossing depth. For example, the emboss depth is preferably 1 mm or less, and more preferably 0.5 mm or less. In order to further improve the smoothness, it is preferable to further perform calendar processing. The apparent density can be improved by calendering. By using the flat roll surface as the foamed resin layer forming surface instead of the embossed roll surface, the resin can be foamed more smoothly than when the foamed resin layer is formed on the embossed roll surface.

本発明の発泡樹脂積層シート用基材は、180℃環境下無張力で3分間保持したときの乾熱寸法変化率が、経方向0%〜−5.0%、緯方向−1.0%〜3.0%であることが好ましい。本発明の発泡樹脂積層シート用基材に発泡樹脂層を形成する際には、例えば発泡性合成樹脂組成物の塗工後、乾燥工程及び樹脂発泡工程という高温処理工程を通る。この場合、基材の乾熱処理での寸法変化が大きいと、製品幅が短くなること、皺が入って製品品位が低下すること等が問題になる。特に、通常、基材上に発泡樹脂層を形成する際、MD(経)方向はロールにより固定されているが、CD(緯)方向は固定されていない場合が多く、CD(緯)方向は特に収縮しやすい。基材を180℃環境下無張力で3分間保持したときの乾熱寸法変化率がMD(経)方向0%〜―5.0%、CD(緯)方向−1%〜3.0%の範囲内にコントロールしている場合、製品品位が良好な発泡樹脂積層シートを製造できる点で有利である。上記乾熱寸法変化率は、MD方向では0%〜−3.5%がより好ましく、CD方向では0%〜3.0%がより好ましい。上記乾熱寸法変化率は、温度180℃の乾燥機中で基材を3分間熱処理し、熱処理前後の寸法から、下記式に従って算出する。
MD方向の乾熱寸法変化率={(熱処理後のMD寸法)−(熱処理前のMD寸法)}/(熱処理前のMD寸法)
CD方向の乾熱寸法変化率={(熱処理後のCD寸法)−(熱処理前のCD寸法)}/(熱処理前のCD寸法)
The base material for a foamed resin laminate sheet of the present invention has a dry heat dimensional change rate of 0% to -5.0% in the warp direction and -1.0% in the weft direction when held for 3 minutes under no tension in an environment of 180 ° C. It is preferable that it is -3.0%. When the foamed resin layer is formed on the base material for the foamed resin laminate sheet of the present invention, for example, after the foamable synthetic resin composition is applied, it passes through a high-temperature treatment process called a drying process and a resin foaming process. In this case, when the dimensional change in the dry heat treatment of the substrate is large, the product width becomes short, and wrinkles enter and the product quality is lowered. In particular, when forming a foamed resin layer on a substrate, the MD (warp) direction is usually fixed by a roll, but the CD (lattice) direction is often not fixed. Especially easy to shrink. When the substrate is held at 180 ° C. under no tension for 3 minutes, the dimensional change rate of dry heat is 0% to −5.0% in the MD (longitudinal) direction and −1% to 3.0% in the CD (longitudinal) direction. Controlling within the range is advantageous in that a foamed resin laminated sheet with good product quality can be produced. The dry heat dimensional change rate is more preferably 0% to -3.5% in the MD direction, and more preferably 0% to 3.0% in the CD direction. The dry heat dimensional change rate is calculated according to the following formula from the dimensions before and after heat treatment of the substrate for 3 minutes in a dryer at a temperature of 180 ° C.
Dry heat dimensional change rate in the MD direction = {(MD dimension after heat treatment) − (MD dimension before heat treatment)} / (MD dimension before heat treatment)
Dry heat dimensional change rate in CD direction = {(CD dimension after heat treatment) − (CD dimension before heat treatment)} / (CD dimension before heat treatment)

ポリエステル系繊維の融点は、200℃以上であることが好ましい。本発明の発泡樹脂積層シート用基材の上に発泡樹脂層を形成する際、通常発泡工程は発泡樹脂面側から加熱し、180℃〜230℃前後で行うため、基材の温度も150℃〜170℃近辺まで上昇すると考えられる。ポリエステル系繊維の融点が200℃以上であれば発泡工程でも基材が断布することなく生産することができる。ポリエステル系繊維の融点は、より好ましくは210〜280℃、更に好ましくは210〜270℃である。なお上記融点は、示差走査熱量計(例えばSIIナノテクノロジー社製のDSC210)を使用し、測定雰囲気:窒素ガス50mL/分 昇温速度:10℃/分で測定を行い、融解ピークの導入部分における変曲点の漸近線とTgより高い温度領域でのベースラインとが交わる温度として求められる値である。   The melting point of the polyester fiber is preferably 200 ° C. or higher. When the foamed resin layer is formed on the base material for the foamed resin laminate sheet of the present invention, the foaming step is usually heated from the foamed resin surface side and is performed at around 180 ° C to 230 ° C. It is thought that it rises to around 170 ° C. If the melting point of the polyester fiber is 200 ° C. or higher, the substrate can be produced without severing even in the foaming process. The melting point of the polyester fiber is more preferably 210 to 280 ° C, still more preferably 210 to 270 ° C. The melting point is measured using a differential scanning calorimeter (for example, DSC210 manufactured by SII Nanotechnology) at a measurement atmosphere: nitrogen gas 50 mL / min, heating rate: 10 ° C./min, and at the melting peak introduction portion. This value is obtained as the temperature at which the asymptotic line of the inflection point intersects with the baseline in the temperature region higher than Tg.

ポリエステル系繊維等の熱可塑性樹脂は、ガラス転移点以上の温度で軟化する。ポリエステル系繊維を主成分とする不織布は、湿潤時に強度が低下しない点で紙基材よりも有利である。しかし、ポリエステル系繊維を主成分とする不織布もガラス転移点以上の温度がかかる環境下で張力がかかると伸びる傾向があるため、発泡樹脂塗工後の乾燥時や発泡の際のロール間張力を、例えば従来の紙基材を使用する場合と比べて低張力に設定することは、品位のよい発泡樹脂積層シートが得られやすい点で好ましい。しかしながら、発泡性樹脂の発泡工程時には基材も150℃〜170℃あたりまで昇温すると考えられるため、ポリエステル系繊維を主成分とする不織布の150℃環境下の熱時破断強度が例えば150N/5cm以上である場合には、特に張力の調整を行わなくても従来の設備を問題なく使用することができ好ましい。なお上記熱時破断強度は、150℃に設定した加熱炉に不織布試験片をセットし、庫内の温度が上記所定の温度に達した時点で破断強度を測定する方法で測定される値である。   Thermoplastic resins such as polyester fibers soften at a temperature above the glass transition point. Nonwoven fabrics composed mainly of polyester fibers are more advantageous than paper bases in that the strength does not decrease when wet. However, non-woven fabrics composed mainly of polyester fibers tend to stretch when tension is applied in an environment where the temperature is higher than the glass transition point. Therefore, the tension between rolls during drying or foaming after foam resin coating is limited. For example, it is preferable to set the tension lower than that in the case of using a conventional paper base material because a foamed resin laminated sheet with good quality can be easily obtained. However, since it is considered that the temperature of the base material is also increased to about 150 ° C. to 170 ° C. during the foaming process of the foamable resin, the thermal break strength in a 150 ° C. environment of a nonwoven fabric mainly composed of polyester fiber is, for example, 150 N / 5 cm. In the case of the above, it is preferable that the conventional equipment can be used without any problem without particularly adjusting the tension. The hot breaking strength is a value measured by a method in which a nonwoven fabric test piece is set in a heating furnace set at 150 ° C., and the breaking strength is measured when the temperature in the cabinet reaches the predetermined temperature. .

本発明の発泡樹脂積層シート用基材は、目付が30〜100g/m2の範囲において細い繊維と太い繊維を混用して形成することが好ましい。この場合、より基材を緻密化し、より好ましい壁紙基材が得られやすい。その混用例を説明する。発泡樹脂層の形成面を与える表面層、該表面層に接する中間層及び該中間層に接する裏面層が熱圧着により一体化されている積層不織布であり、かつ下記(1)〜(3):
(1)表面層が、繊維径7〜30μmの熱可塑性樹脂長繊維からなる層を少なくとも1層有すること、
(2)中間層が、繊維径1〜5μmのメルトブロウン繊維からなる層を少なくとも1層有し、目付が1g/m2以上であり、かつ積層不織布の目付の30質量%以下を構成すること、及び
(3)裏面層が、繊維径7〜30μmの熱可塑性樹脂長繊維からなる層を少なくとも1層有し、かつ目付が3〜40g/m2であること
を満足する基材は、より好ましく発泡樹脂積層シートを製造することができる。本発明の基材が、表面層、中間層及び裏面層が熱圧着により一体化されている積層不織布である場合、基材の均一性が高く、中間層であるメルトブロウン層が発泡樹脂層形成時の樹脂の裏抜けを防止するためいっそう好ましい。
The base material for a foamed resin laminate sheet of the present invention is preferably formed by mixing thin fibers and thick fibers in the range of 30 to 100 g / m 2 in basis weight. In this case, the base material is further densified, and a more preferable wallpaper base material is easily obtained. A mixed example will be described. A surface non-woven fabric in which a surface layer for forming a foamed resin layer, an intermediate layer in contact with the surface layer, and a back layer in contact with the intermediate layer are integrated by thermocompression bonding, and the following (1) to (3):
(1) The surface layer has at least one layer of thermoplastic resin long fibers having a fiber diameter of 7 to 30 μm,
(2) The intermediate layer has at least one layer composed of melt-blown fibers having a fiber diameter of 1 to 5 μm, has a basis weight of 1 g / m 2 or more, and constitutes 30% by mass or less of the basis weight of the laminated nonwoven fabric. And (3) the base material satisfying that the back surface layer has at least one layer made of a thermoplastic resin long fiber having a fiber diameter of 7 to 30 μm and the basis weight is 3 to 40 g / m 2. Preferably, a foamed resin laminated sheet can be produced. When the base material of the present invention is a laminated nonwoven fabric in which the surface layer, the intermediate layer, and the back layer are integrated by thermocompression bonding, the base material has high uniformity, and the melt blown layer that is the intermediate layer forms a foamed resin layer. It is more preferable in order to prevent the resin from slipping through.

表面層には、平滑でかつ発泡性樹脂が適度にしみこみ発泡性樹脂と基材を密着させる機能が必要である。繊維径が7〜30μmであれば表面の平滑性を維持し、基材を密着させる見かけ密度にコントロールしやすい。このうち基材の最表面をなす層は、上記ポリエステル系繊維から選択される長繊維からなり、繊維径は、好ましくは7〜30μm、より好ましくは7〜20μmの範囲である。上記繊維径が7μm未満では、カレンダー加工時に圧着が効きすぎフィルム化しやすくなるため生産条件のコントロールが難しくなり、発泡性樹脂との密着性が低下しやすくなる。30μmを超えると表面の平滑性が低下する傾向がある。   The surface layer must be smooth and have a function of adhering the foamable resin and the substrate in a proper manner with the foamable resin soaked appropriately. If the fiber diameter is 7 to 30 μm, the smoothness of the surface is maintained and the apparent density at which the substrate is brought into close contact is easily controlled. Among these, the layer which makes the outermost surface of a base material consists of the long fiber selected from the said polyester fiber, and a fiber diameter becomes like this. Preferably it is 7-30 micrometers, More preferably, it is the range of 7-20 micrometers. When the fiber diameter is less than 7 μm, pressure bonding is too effective at the time of calendering, and it becomes easy to form a film. Therefore, it becomes difficult to control production conditions, and adhesion with a foaming resin tends to be lowered. When it exceeds 30 μm, the smoothness of the surface tends to decrease.

中間層のうち少なくとも1つの層は、例えば上記ポリエステル系繊維等から選択されるメルトブロウン繊維からなり、繊維径は、好ましくは1〜5μm、より好ましくは1〜3μmの範囲である。中間層の極細繊維層はより緻密な層を形成し、発泡樹脂の更なるしみこみ(裏抜け)を防止する働きをする。上記繊維径が1μm未満では基材の生産性が低下する傾向があり、5μmを超えると繊維間隙が大きくなりすぎ、発泡樹脂のコーティング時の裏抜け防止性が十分発揮できない傾向がある。   At least one of the intermediate layers is made of, for example, meltblown fibers selected from the above-described polyester fibers and the like, and the fiber diameter is preferably in the range of 1 to 5 μm, more preferably 1 to 3 μm. The ultrafine fiber layer of the intermediate layer forms a denser layer and functions to prevent further penetration (back-through) of the foamed resin. When the fiber diameter is less than 1 μm, the productivity of the base material tends to decrease. When the fiber diameter exceeds 5 μm, the fiber gap becomes too large, and there is a tendency that the anti-through-through prevention property at the time of coating with the foamed resin cannot be exhibited sufficiently.

この中間層に使用されるメルトブロウン繊維はバインダー繊維の働きも有し、裏面層と表面層とを強固に接着し層間剥離や繊維の脱落の防止を助ける機能を有する。中間層の目付が1g/m2未満では発泡樹脂の裏抜け防止機能や繊維間の接着機能が低下する傾向がある。 The meltblown fiber used for this intermediate layer also has the function of a binder fiber, and has a function of firmly adhering the back surface layer and the surface layer to help prevent delamination and fiber loss. If the basis weight of the intermediate layer is less than 1 g / m 2 , the function of preventing foam from falling through and the function of bonding between fibers tend to deteriorate.

中間層の目付は、発泡樹脂の裏抜け防止性の観点から好ましくは1g/m2以上であり、より好ましくは3g/m2〜25g/m2である。また中間層は、積層不織布の目付に対して30質量%以下を構成することが好ましい。30質量%を超えると基材の見かけ密度が高くなりすぎる傾向にある。中間層は、積層不織布の目付の1.5質量%〜30質量%を構成することがより好ましく、3質量%〜25質量%を構成することが更に好ましい。 Basis weight of the intermediate layer is preferably from the viewpoint of prevention of strike-through of the foamed resin is at 1 g / m 2 or more, and more preferably from 3g / m 2 ~25g / m 2 . Moreover, it is preferable that an intermediate | middle layer comprises 30 mass% or less with respect to the fabric weight of a laminated nonwoven fabric. If it exceeds 30% by mass, the apparent density of the substrate tends to be too high. The intermediate layer more preferably constitutes 1.5% by mass to 30% by mass of the basis weight of the laminated nonwoven fabric, and further preferably constitutes 3% by mass to 25% by mass.

裏面層のうちの少なくとも1つの層、好ましくは基材の最裏面をなす層は、例えば表面層において前述したのと同様のものから選択できる熱可塑性樹脂の長繊維からなり、繊維径は、好ましくは7〜30μm、より好ましくは7〜20μmの範囲である。該基材を生産する際、通常は、裏面層を形成した上に引き続き中間層を形成する方法をとっている。これにより、中間層は裏面層の繊維間に絡まるように形成され、裏面層により固定される。このため、裏面層の繊維径が30μmを超えると長繊維同士の繊維間隙が広くなりすぎ、メルトブロウン繊維を十分に固定することができなくなり、発泡樹脂層の形成(例えばコーティング)時に生じる圧力によりメルトブロウン繊維が移動して中間層の繊維間隙が大きくなるため、結果的に裏抜け防止性が十分発揮できない傾向がある。一方、上記繊維径が7μm未満では繊維間隙がメルトブロウン層(中間層)に近くなり、メルトブロウン層に滞留している発泡性樹脂(例えばコーティング樹脂)を毛細管力により吸引する力が強くなるため、十分な裏抜け防止性が発揮できない傾向がある。   At least one layer of the back surface layer, preferably the layer forming the backmost surface of the base material, is made of a long fiber of a thermoplastic resin that can be selected from, for example, the same as described above in the surface layer, and the fiber diameter is preferably Is in the range of 7-30 μm, more preferably 7-20 μm. When producing this base material, the method of forming an intermediate | middle layer normally after forming a back layer normally is taken. Thereby, an intermediate | middle layer is formed so that it may get entangled between the fibers of a back surface layer, and is fixed by the back surface layer. For this reason, when the fiber diameter of the back surface layer exceeds 30 μm, the fiber gap between the long fibers becomes too wide to sufficiently fix the meltblown fibers, and due to the pressure generated during the formation of the foamed resin layer (for example, coating) Since the meltblown fibers move and the fiber gaps in the intermediate layer increase, there is a tendency that as a result, the back-through prevention property cannot be sufficiently exhibited. On the other hand, when the fiber diameter is less than 7 μm, the fiber gap is close to the meltblown layer (intermediate layer), and the force to suck the foamable resin (for example, coating resin) staying in the meltblown layer by capillary force becomes strong. , There is a tendency that sufficient anti-cracking prevention properties cannot be exhibited.

裏面層の目付は、中間層であるメルトブロウン繊維を固定し、発泡性樹脂の裏抜けを防止する観点から好ましくは3〜40g/m2である。 The basis weight of the back layer is preferably 3 to 40 g / m 2 from the viewpoint of fixing the melt-blown fiber as the intermediate layer and preventing the foaming resin from being pulled through.

発泡樹脂積層シート用基材として、メルトブロウン繊維を積層した不織布を用いる場合、フラットロールにて熱圧着する場合には一般的に表面層を樹脂形成(塗工)面とするが、裏面層を樹脂塗工面に用いても何ら差し支えない。また、エンボスロールにて熱圧着する場合には、フラットロール面(裏面層)を樹脂塗工層とすることが平滑性の観点でより望ましい。しかしカレンダー加工を行う場合はこの限りではない。   When using a nonwoven fabric laminated with meltblown fibers as the base material for the foamed resin laminate sheet, when thermocompression bonding is performed with a flat roll, the surface layer is generally the resin-formed (coated) surface, but the back layer is There is no problem even if it is used on the resin coated surface. Moreover, when thermocompression bonding is performed with an embossing roll, it is more desirable from the viewpoint of smoothness that the flat roll surface (back surface layer) is a resin coating layer. However, this is not the case when performing calendar processing.

[発泡樹脂積層シート用基材の製造]
本発明の発泡樹脂積層シート用基材となる不織布は、従来公知のスパンボンド(SB)法、フラッシュ紡糸法、スパンレース法、ニードルパンチ法、抄造法等で製造できる。特にスパンボンド法から得られる長繊維不織布は好ましい。なお基材が積層構造を有する場合には各層を互いに同じ又は異なる方法で形成できる。
[Manufacture of base material for foamed resin laminate sheet]
The nonwoven fabric used as the base material for the foamed resin laminate sheet of the present invention can be produced by a conventionally known spunbond (SB) method, flash spinning method, spunlace method, needle punch method, papermaking method or the like. In particular, a long fiber nonwoven fabric obtained from the spunbond method is preferred. In addition, when a base material has a laminated structure, each layer can be formed by the same or different method.

発泡樹脂積層シート用基材の製造においては、通常熱圧着工程を行う。熱圧着は、ポリエステル系繊維の融点よりも例えば50℃から120℃低い温度で、線圧100〜1000N/cmでフラットロール又はエンボスロールを用いて繊維間(積層構造においては繊維間及び層間)を接合できる。本発明の基材はカレンダー処理されていることがより好ましい。カレンダー処理されることにより、基材表面がより平滑になり、発泡性樹脂発泡後の表面品位がよくなる。また、基材の繊維間の接着強度が増し、繊維くずが脱落しにくくなる他、基材の強度アップにもつながる。この場合、上記の熱圧着後に、例えば熱圧着温度よりも10℃以上高く且つポリエステル系繊維の融点より10〜100℃低い温度で線圧100〜1000N/cmでカレンダー処理することにより、良好な強度が得られ、見かけ密度を制御することができる。カレンダー処理における温度が、ポリエステル系繊維の融点より低く、その温度差が10℃未満である場合には、見かけ密度が高くなりすぎる場合があり、一方その温度差が100℃を超える場合には、乾熱寸法変化率を所定の範囲内に制御することができず、強度が低くなる場合がある。   In the production of the base material for the foamed resin laminated sheet, a thermocompression bonding step is usually performed. Thermocompression bonding is performed at a temperature lower than the melting point of the polyester fiber by, for example, 50 ° C. to 120 ° C., using a flat roll or an emboss roll at a linear pressure of 100 to 1000 N / cm (between fibers and between layers in a laminated structure). Can be joined. The base material of the present invention is more preferably calendered. By performing the calendar treatment, the surface of the base material becomes smoother and the surface quality after foaming of the foamable resin is improved. In addition, the adhesive strength between the fibers of the base material is increased, fiber waste is less likely to fall off, and the strength of the base material is increased. In this case, after the above-described thermocompression bonding, for example, calendering is performed at a linear pressure of 100 to 1000 N / cm at a temperature higher than the thermocompression bonding temperature by 10 ° C. or more and 10 to 100 ° C. lower than the melting point of the polyester fiber, thereby obtaining good strength And the apparent density can be controlled. If the temperature in the calendering process is lower than the melting point of the polyester fiber and the temperature difference is less than 10 ° C, the apparent density may be too high, whereas if the temperature difference exceeds 100 ° C, The dry heat dimensional change rate cannot be controlled within a predetermined range, and the strength may be lowered.

熱圧着工程及びカレンダー処理における線圧が100N/cm未満であると良好な接着が得られにくく、良好な強度が発現されにくい傾向がある。また線圧が1000N/cmを超えると繊維の変形が大きくなりすぎ、見かけ密度が高くなりすぎて本発明の範囲内とすることが難しい傾向がある。   When the linear pressure in the thermocompression bonding process and the calendar process is less than 100 N / cm, it is difficult to obtain good adhesion, and good strength tends not to be expressed. On the other hand, when the linear pressure exceeds 1000 N / cm, the deformation of the fiber becomes too large, the apparent density becomes too high, and it tends to be difficult to make it within the scope of the present invention.

本発明の発泡樹脂積層シート用基材には後加工により難燃性を付与することができる。例えば燃焼カロリーを低下させるために水酸化アルミニウム等が好ましく用いられる。   Flame retardancy can be imparted to the base material for a foamed resin laminate sheet of the present invention by post-processing. For example, aluminum hydroxide or the like is preferably used in order to reduce the burned calories.

[発泡樹脂積層シート]
本発明の発泡樹脂積層シート用基材は、発泡樹脂積層シート用基材と、該発泡樹脂積層シート用基材上に形成された発泡樹脂層とを有し、該発泡樹脂層が、発泡剤を含む発泡性合成樹脂組成物の加熱発泡により形成されている、発泡樹脂積層シートを提供するために使用できる。
[Foamed resin laminate sheet]
The base material for a foamed resin laminate sheet of the present invention has a base material for a foam resin laminate sheet and a foam resin layer formed on the base material for the foam resin laminate sheet, and the foam resin layer is a foaming agent. Can be used to provide a foamed resin laminate sheet formed by heating and foaming a foamable synthetic resin composition.

発泡樹脂層は合成樹脂(通常は軟質樹脂)から形成される。軟質樹脂としては、ポリ塩化ビニル樹脂(PVC)、EVA、ポリオレフィン樹脂等を使用できる。   The foamed resin layer is formed from a synthetic resin (usually a soft resin). As the soft resin, polyvinyl chloride resin (PVC), EVA, polyolefin resin, or the like can be used.

発泡剤としては、一般的に使用されているアゾジカルボアミドの他、オキシビスベンゼンスルフォニルヒドラジド、ベンゼンスルフォニルヒドラジド、p−トルエンスルフォニルヒドラジド、ジアゾアミノベンゼン、アゾビスイソブチロニトリル等の熱分解型有機系発泡剤が使用できる。これらの発泡剤は2種以上併用することができる。また発泡剤の添加量は所望の発泡倍率、使用する発泡剤の種類等により適宜添加することができる。   As the blowing agent, in addition to the commonly used azodicarboxamides, thermal decomposition types such as oxybisbenzenesulfonyl hydrazide, benzenesulfonyl hydrazide, p-toluenesulfonyl hydrazide, diazoaminobenzene, azobisisobutyronitrile, etc. Organic foaming agents can be used. Two or more of these foaming agents can be used in combination. Moreover, the addition amount of a foaming agent can be suitably added with the desired foaming ratio, the kind of foaming agent to be used, etc.

発泡剤を含む発泡性合成樹脂組成物は、上述の合成樹脂、上述の発泡剤、及び可塑剤、更に任意に安定剤、充填剤、顔料等からなる。好ましい発泡性合成樹脂組成物の組成としては、例えば、合成樹脂が塩化ビニル系樹脂である場合は、塩化ビニル樹脂単独又は塩化ビニルと酢酸ビニル、エチレン、プロピレン、マレイン酸エステル、メタクリル酸エステル等との共重合体から選択される1種以上の合成樹脂100質量部に対して、1種以上の発泡剤を0.5〜10質量部、及び可塑剤を50〜100質量部、更に任意成分として、安定剤、充填剤及び顔料を含有させたものが挙げられる。   The foamable synthetic resin composition containing a foaming agent comprises the above-described synthetic resin, the above-mentioned foaming agent, and a plasticizer, and optionally a stabilizer, a filler, a pigment, and the like. As the composition of the preferred foamable synthetic resin composition, for example, when the synthetic resin is a vinyl chloride resin, the vinyl chloride resin alone or vinyl chloride and vinyl acetate, ethylene, propylene, maleate, methacrylate, etc. As an optional component, 0.5 to 10 parts by mass of one or more foaming agents, 50 to 100 parts by mass of a plasticizer, and 100 parts by mass of one or more kinds of synthetic resins selected from the copolymer of , Stabilizers, fillers and pigments.

上述のような発泡性合成樹脂組成物を基材上にナイフコーター等により塗工し、樹脂の仕様に応じた発泡条件を適宜選択して加熱発泡させることにより、基材上に発泡樹脂層を形成できる。発泡樹脂層には、発泡後常套の方法による模様付け又はエンボス等の表面処理が施されていてもよい。   The foamable synthetic resin composition as described above is coated on a substrate with a knife coater or the like, and foamed resin layers are formed on the substrate by appropriately selecting foaming conditions according to the resin specifications and heating and foaming. Can be formed. The foamed resin layer may be subjected to surface treatment such as patterning or embossing by a conventional method after foaming.

以下、実施例を用いて本発明を更に具体的に説明するが本発明はこれらにより何ら限定されるものではない。本発明の特性は、下記の方法で測定した。   Hereinafter, the present invention will be described more specifically with reference to examples, but the present invention is not limited thereto. The characteristics of the present invention were measured by the following methods.

(1) 目付(g/m2
縦20cm×横25cmの試料を3カ所切り取り、質量を測定し、その数平均値を単位面積当たりの質量に換算して求めた(JIS−L−1906に準拠)。
(2) 厚み(μm)
接圧荷重100g/cm2にて幅方向に10箇所測定し、その数平均値を厚みとした。厚み計は、PEACOCK製No.207を用いた。最小目盛が0.01であるため、小数点第3位まで読み取って平均した後、有効数字を2桁としてμmに換算した(JIS−L−1906に準拠)。
(3) 見かけ密度(g/cm3
上記(1)にて測定した目付(g/m2)、及び上記(2)にて測定した厚み(μm)を用い、以下の式により算出した。
見かけ密度=(目付)/(厚み)
(4) 平均繊維径(μm)
試料(不織布)の両端部10cmを除いて、試料の幅20cm毎の区域から、それぞれ1cm角の試験片を切り取った。各試験片について、マイクロスコープで繊維の直径を30点測定して、測定値の数平均値(小数点第2位を四捨五入)を算出し、試料を構成する繊維の平均繊維径とした。
(5) 破断強度(引張強力)(N/5cm)
試料の両端部10cmを除き、幅5cm×長さ20cmの試験片を切り取った。以下の条件で測定したときの試験片の最大荷重時の強さの5箇所での数平均値をMD(経方向)で求めた。
把持長:10cm 引張速度:10cm/分
(1) Weight per unit (g / m 2 )
Samples measuring 20 cm in length and 25 cm in width were cut out at three locations, mass was measured, and the number average value was converted into mass per unit area (based on JIS-L-1906).
(2) Thickness (μm)
Ten locations in the width direction were measured at a contact pressure load of 100 g / cm 2 , and the number average value was taken as the thickness. The thickness gauge is a PEACOCK No. 207 was used. Since the minimum scale was 0.01, after reading to the third decimal place and averaging, it was converted to μm with 2 significant figures (conforming to JIS-L-1906).
(3) Apparent density (g / cm 3 )
Using the basis weight (g / m 2 ) measured in the above (1) and the thickness (μm) measured in the above (2), it was calculated by the following formula.
Apparent density = (weight) / (thickness)
(4) Average fiber diameter (μm)
Except for 10 cm at both ends of the sample (nonwoven fabric), 1 cm square test pieces were cut out from the area of each 20 cm width of the sample. About each test piece, the diameter of the fiber was measured at 30 points with a microscope, the number average value of the measured values (rounded to the first decimal place) was calculated, and the average fiber diameter of the fibers constituting the sample was obtained.
(5) Breaking strength (tensile strength) (N / 5cm)
A test piece having a width of 5 cm and a length of 20 cm was cut out except for 10 cm at both ends of the sample. The number average value at five locations of the strength at the maximum load of the test piece when measured under the following conditions was determined by MD (longitudinal direction).
Gripping length: 10 cm Tensile speed: 10 cm / min

(6) 熱時破断強度(熱時引張強力)(N/5cm)
上記(5)と同様形状に作製した試料を、所定の温度(150℃)に設定した加熱炉にセットし、庫内の温度が上記所定の温度に達した時点で(5)と同様の条件で試料を伸張して破断強度を求めた。
(7) 乾熱寸法変化率
サンプルを30cm×30cmにサンプリングし、経緯それぞれ20cm間隔で5箇所印をつけた。この試料を3枚準備し、温度180℃で3分間、乾燥機で熱処理し、熱処理前後の印間寸法から、下記式に従って算出した。
MD方向の乾熱寸法変化率={(熱処理後のMD寸法)−(熱処理前のMD寸法)}/(熱処理前のMD寸法)
CD方向の乾熱寸法変化率={(熱処理後のCD寸法)−(熱処理前のCD寸法)}/(熱処理前のCD寸法)
(8) 表面の凹凸度(μm)
コスム社製 非接触高速3次元形状システム MAP―3Dを使用し、発泡樹脂層のコーティング面となる基材表面の凹凸度を測定した。試料をスライドガラスに両面テープで固定し、20mm間について100μmピッチで表面凹凸を測定した。隣り合う山と谷間の高さを20個測定し数平均した。特定の周期で凹凸を繰り返す柄(たとえばエンボス)が存在する場合には柄の凹凸の山谷間の高さを測定した。この数値が小さいほど表面の平滑性に優れる。
(6) Hot breaking strength (thermal tensile strength) (N / 5cm)
A sample prepared in the same shape as in (5) above is set in a heating furnace set at a predetermined temperature (150 ° C.), and the same conditions as in (5) at the time when the internal temperature reaches the predetermined temperature. The sample was stretched to obtain the breaking strength.
(7) Dry heat dimensional change rate Samples were sampled to 30 cm x 30 cm, and 5 points were marked at intervals of 20 cm. Three samples were prepared, heat-treated with a dryer at a temperature of 180 ° C. for 3 minutes, and calculated according to the following formula from the dimension between the marks before and after the heat treatment.
Dry heat dimensional change rate in the MD direction = {(MD dimension after heat treatment) − (MD dimension before heat treatment)} / (MD dimension before heat treatment)
Dry heat dimensional change rate in CD direction = {(CD dimension after heat treatment) − (CD dimension before heat treatment)} / (CD dimension before heat treatment)
(8) Surface roughness (μm)
Using a non-contact high-speed three-dimensional shape system MAP-3D manufactured by Cosm Co., Ltd., the degree of unevenness on the surface of the base material to be the coating surface of the foamed resin layer was measured. The sample was fixed to a slide glass with double-sided tape, and surface irregularities were measured at a pitch of 100 μm between 20 mm. Twenty heights between adjacent peaks and valleys were measured and number averaged. When there was a pattern (for example, embossing) that repeated unevenness at a specific period, the height between the peaks and valleys of the uneven pattern was measured. The smaller this value, the better the surface smoothness.

(9) 樹脂裏抜け防止性
ステンレス板上に固定した基材の上に、下記配合からなる塩化ビニル樹脂組成物を0.2mmの厚さにナイフコーターでコーティングしたのち、ステンレス板上の樹脂汚れの発生の有無を確認した。
評価は下記の基準で行った。
良好:ステンレス板上に樹脂の付着が見られないもの
不良:ステンレス板上に樹脂が付着しているもの。
塩化ビニル樹脂組成物配合
ペースト塩化ビニル樹脂 43質量%
ジオクチルフタレート 20質量%
重質炭酸カルシウム 35質量%
発泡剤(アゾジカルボンアミド) 2質量%
(9) Resin back-through prevention property After coating a vinyl chloride resin composition having the following composition on a base material fixed on a stainless steel plate to a thickness of 0.2 mm with a knife coater, resin stains on the stainless steel plate The presence or absence of occurrence was confirmed.
Evaluation was performed according to the following criteria.
Good: No adhesion of the resin on the stainless steel plate. Bad: The resin is adhered on the stainless steel plate.
Compound containing vinyl chloride resin Paste vinyl chloride resin 43% by mass
Dioctyl phthalate 20% by mass
Heavy calcium carbonate 35% by mass
Foaming agent (azodicarbonamide) 2% by mass

[実施例1〜7]
裏面層としてPET長繊維ウェブを形成した。汎用PET(ポリエチレンテレフタレート)を、スパンボンド法により、紡糸温度300℃で、フィラメント群を移動する捕集ネット面に向けて押し出し、紡糸速度3500m/分で紡糸し、コロナ帯電で3μC/g程度帯電させて十分に開繊させ、PET長繊維ウェブを捕集ネット上に調整した。繊維径の調整は、吐出量を変えることにより行った。
[Examples 1-7]
A PET continuous fiber web was formed as the back layer. General-purpose PET (polyethylene terephthalate) is extruded by spunbonding at a spinning temperature of 300 ° C. toward the collection net surface that moves the filament group, spun at a spinning speed of 3500 m / min, and charged at a corona charge of about 3 μC / g. The PET continuous fiber web was prepared on a collection net. The fiber diameter was adjusted by changing the discharge amount.

次いで、中間層としてメルトブロウン繊維からなる層を形成した。PET(溶液粘度:ηsp/c=0.5)を、紡糸温度300℃、加熱空気1000Nm3/hr/mの条件下で、メルトブロウン法により紡糸して、上記のPET長繊維ウェブ上に吹き付けた。この際、メルトブロウンノズルから長繊維ウェブまでの距離を100mmとし、メルトブロウンノズル直下の捕集面における吸引力を0.2kPa、風速を7m/秒に設定した。繊維径の調整は、吐出量を変えることにより行った。 Next, a layer made of meltblown fibers was formed as an intermediate layer. PET (solution viscosity: ηsp / c = 0.5) was spun by the meltblown method under a spinning temperature of 300 ° C. and heated air of 1000 Nm 3 / hr / m and sprayed onto the PET long fiber web. It was. At this time, the distance from the meltblown nozzle to the long fiber web was set to 100 mm, the suction force at the collection surface immediately below the meltblown nozzle was set to 0.2 kPa, and the wind speed was set to 7 m / sec. The fiber diameter was adjusted by changing the discharge amount.

更に、上記で得た裏面層と中間層とからなる積層ウェブの中間層側に直接、裏面層のPET長繊維ウェブと同様の方法で、表面層としてPET長繊維を所定の繊維径及び繊維量(目付)になるように積層した。上記により、表面層:PET長繊維(S1)/中間層:メルトブロウン繊維(M)/裏面層:PET長繊維(S2)からなる積層ウェブを得た。得られた積層ウェブを、フラットロールにて熱圧着した後、カレンダーロールにて厚み調整を行い、表1に示す見かけ密度の積層不織布を得た。
熱圧着条件:線圧265N/cm ロール温度 表面側/裏面側(180℃/180℃)
カレンダー条件:線圧663N/cm ロール温度 表面側/裏面側(236℃/231℃)
Further, a PET continuous fiber is used as a surface layer in the same manner as the PET continuous fiber web of the back layer directly on the intermediate layer side of the laminated web composed of the back layer and the intermediate layer obtained above, and a predetermined fiber diameter and fiber amount. The layers were laminated so as to have a basis weight. As described above, a laminated web composed of surface layer: PET long fiber (S1) / intermediate layer: meltblown fiber (M) / back layer: PET long fiber (S2) was obtained. The obtained laminated web was thermocompression bonded with a flat roll, and then the thickness was adjusted with a calendar roll to obtain a laminated nonwoven fabric having an apparent density shown in Table 1.
Thermocompression bonding conditions: Linear pressure 265 N / cm Roll temperature Front side / Back side (180 ° C / 180 ° C)
Calendar conditions: Linear pressure 663 N / cm Roll temperature Front side / Back side (236 ° C./231° C.)

[実施例8]
上記の汎用PETに代えて融点205℃の共重合PETを用い、紡糸温度を280℃にした以外は、実施例1と同様の方法で長繊維不織布を得た。更にカレンダーロールにて厚み調整した。カレンダー条件は実施例1と同様の条件とした。
[Example 8]
A long fiber nonwoven fabric was obtained in the same manner as in Example 1 except that copolymer PET having a melting point of 205 ° C. was used in place of the general-purpose PET and the spinning temperature was 280 ° C. Furthermore, the thickness was adjusted with a calendar roll. The calendar conditions were the same as in Example 1.

参考例9]
実施例1と同様の方法で得られた積層ウェブ(S1)/(M)/(S2)をエンボス比率14%の格子柄エンボスロールにて熱圧着し、表2に示す見かけ密度の積層不織布を得た。
[ Reference Example 9]
The laminated web (S1) / (M) / (S2) obtained by the same method as in Example 1 was thermocompression bonded with a lattice pattern embossing roll having an embossing ratio of 14%, and laminated nonwoven fabrics having an apparent density shown in Table 2 were obtained. Obtained.

参考例10]
参考例9で得られた積層不織布(S1)/(M)/(S2)をさらにカレンダーロールにて厚み調整した。カレンダー条件は実施例1と同様の条件とした。
[ Reference Example 10]
The laminated nonwoven fabric (S1) / (M) / (S2) obtained in Reference Example 9 was further thickness adjusted with a calender roll. The calendar conditions were the same as in Example 1.

参考例11]
実施例1の裏面層と表面層とを表中に示す所定の繊維径及び繊維量(目付)になるように積層して、表面層:PET長繊維(S1)/裏面層:PET長繊維(S2)からなる積層ウェブを得た。得られた積層ウェブをエンボス比率14%の格子柄エンボスロールにて熱圧着し、表2に示す見かけ密度の積層不織布を得た。
[ Reference Example 11]
The back layer and the surface layer of Example 1 are laminated so as to have a predetermined fiber diameter and fiber amount (weight per unit area) shown in the table, and the surface layer: PET long fiber (S1) / back surface layer: PET long fiber ( A laminated web consisting of S2) was obtained. The obtained laminated web was thermocompression bonded with a lattice pattern embossing roll having an embossing ratio of 14% to obtain a laminated nonwoven fabric having an apparent density shown in Table 2.

参考例12]
繊維径7μm、繊維長5mm、酸化チタン含有率0.5質量%の延伸短繊維ポリエチレンテレフタレートと繊維径11μm、繊維長5mm、酸化チタン含有率0.5質量%の未延伸短繊維ポリエチレンテレフタレートとを7:3(質量比)の割合で混綿し、抄造法にてネット上に捕集し、120℃で乾燥した後70g/m2の短繊維ウェブを得た。得られたウェブを線圧663N/cm、ロール温度235℃でカレンダー加工した。
[ Reference Example 12]
A stretched short fiber polyethylene terephthalate having a fiber diameter of 7 μm, a fiber length of 5 mm, and a titanium oxide content of 0.5% by mass, and an unstretched short fiber polyethylene terephthalate having a fiber diameter of 11 μm, a fiber length of 5 mm, and a titanium oxide content of 0.5% by mass. The mixture was mixed at a ratio of 7: 3 (mass ratio), collected on a net by a papermaking method, and dried at 120 ° C. to obtain a short fiber web of 70 g / m 2 . The obtained web was calendered at a linear pressure of 663 N / cm and a roll temperature of 235 ° C.

[比較例1]
興人社製 WK−70NTS難燃裏打紙(目付 70g/m2)を使用した。
[Comparative Example 1]
WK-70NTS flame-retardant backing paper (weight per unit area: 70 g / m 2 ) manufactured by Kojin Co., Ltd. was used.

[比較例2]
参考例11と同様の方法で得られた積層ウェブをエンボス比率11%の矩形柄エンボスロールにて熱圧着し、表2に示す見かけ密度の積層不織布を得た。
[比較例3]
参考例11と同様の方法で得られた積層ウェブをエンボス比率11%の矩形柄エンボスロールにて熱圧着し、表2に示す見かけ密度の積層不織布を得た。
[Comparative Example 2]
A laminated web obtained by the same method as in Reference Example 11 was thermocompression bonded with a rectangular pattern embossing roll having an embossing ratio of 11% to obtain a laminated nonwoven fabric having an apparent density shown in Table 2.
[Comparative Example 3]
A laminated web obtained by the same method as in Reference Example 11 was thermocompression bonded with a rectangular pattern embossing roll having an embossing ratio of 11% to obtain a laminated nonwoven fabric having an apparent density shown in Table 2.

Figure 0005486283
Figure 0005486283

Figure 0005486283
Figure 0005486283

本発明の発泡樹脂積層シート用基材は、樹脂との密着性がよく直接発泡樹脂層をコーティング等により形成でき、強度が高く、改装時に剥がす際破れたりすることなくきれいに剥がすことができるため施工作業の効率を向上させることができる。また、該基材を用いて形成した内装材は寸法安定性がよく、長期間の使用時に目地が開く等の不具合が生じにくいという利点を有する。   The base material for the foamed resin laminate sheet of the present invention has good adhesion to the resin, can directly form the foamed resin layer by coating, etc., has high strength, and can be peeled cleanly without tearing when peeled during refurbishment. The work efficiency can be improved. Moreover, the interior material formed using this base material has the advantage that it has good dimensional stability and is less prone to problems such as opening joints during long-term use.

Claims (4)

基材と該基材上に形成された発泡樹脂層とを有する発泡樹脂積層シートを形成するために用いる該基材であって、
ポリエステル系繊維を主成分とする見かけ密度0.3〜0.9g/cm3の不織布であり、発泡樹脂層の形成面となる表面の凹凸度が、1〜30μmであり、
該基材は、該発泡樹脂層の形成面を与える表面層、該表面層に接する中間層及び該中間層に接する裏面層が熱圧着により一体化されている積層不織布であり、かつ下記(1)〜(3):
(1)表面層が、繊維径7〜30μmの熱可塑性樹脂長繊維からなる層を少なくとも1層有すること、
(2)中間層が、繊維径1〜5μmのメルトブロウン繊維からなる層を少なくとも1層有し、目付が1g/m 2 以上であり、かつ積層不織布の目付の30質量%以下を構成すること、及び
(3)裏面層が、繊維径7〜30μmの熱可塑性樹脂長繊維からなる層を少なくとも1層有し、かつ目付が3〜40g/m 2 であること
を満足する、発泡樹脂積層シート用基材。
The base material used for forming a foamed resin laminate sheet having a base material and a foamed resin layer formed on the base material,
A nonwoven fabric apparent density 0.3-0.9 g / cm 3 composed mainly of polyester fibers, irregularities of the surface to be formed surface of the foamed resin layer, Ri. 1 to 30 [mu] m der,
The base material is a laminated non-woven fabric in which a surface layer that provides a surface for forming the foamed resin layer, an intermediate layer in contact with the surface layer, and a back surface layer in contact with the intermediate layer are integrated by thermocompression bonding, and the following (1 ) To (3):
(1) The surface layer has at least one layer of thermoplastic resin long fibers having a fiber diameter of 7 to 30 μm,
(2) The intermediate layer has at least one layer composed of melt-blown fibers having a fiber diameter of 1 to 5 μm, has a basis weight of 1 g / m 2 or more, and constitutes 30% by mass or less of the basis weight of the laminated nonwoven fabric. ,as well as
(3) the back surface layer, a layer made of thermoplastic resin long fibers having a fiber diameter of 7~30μm having at least one layer, and the basis weight is 3~40g / m 2
A base material for a foamed resin laminated sheet that satisfies the requirements.
繊維径1〜30μmの繊維からなり、目付が30〜100g/m2であり、かつ厚みが35〜300μmである、請求項1に記載の発泡樹脂積層シート用基材。 The base material for foamed resin laminated sheets according to claim 1, comprising fibers having a fiber diameter of 1 to 30 µm, a basis weight of 30 to 100 g / m 2 , and a thickness of 35 to 300 µm. 180℃環境下無張力で3分間保持したときの乾熱寸法変化率が、経方向0%〜−5.0%、緯方向−1.0%〜3.0%である、請求項1又は2に記載の発泡樹脂積層シート用基材。   The dimensional change rate of dry heat when held for 3 minutes under no tension in an environment of 180 ° C is 0% to -5.0% in the warp direction and -1.0% to 3.0% in the weft direction. The base material for foamed resin laminated sheets of 2. カレンダー処理されている、請求項1〜のいずれか1項に記載の発泡樹脂積層シート用基材。 The base material for foamed resin laminated sheets according to any one of claims 1 to 3 , which is subjected to a calendar treatment.
JP2009278651A 2009-12-08 2009-12-08 Base material for foamed resin laminate sheet Active JP5486283B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2009278651A JP5486283B2 (en) 2009-12-08 2009-12-08 Base material for foamed resin laminate sheet

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2009278651A JP5486283B2 (en) 2009-12-08 2009-12-08 Base material for foamed resin laminate sheet

Publications (2)

Publication Number Publication Date
JP2011121192A JP2011121192A (en) 2011-06-23
JP5486283B2 true JP5486283B2 (en) 2014-05-07

Family

ID=44285610

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2009278651A Active JP5486283B2 (en) 2009-12-08 2009-12-08 Base material for foamed resin laminate sheet

Country Status (1)

Country Link
JP (1) JP5486283B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2013023782A (en) * 2011-07-21 2013-02-04 Unitika Ltd Foamed wallpaper
JP6929167B2 (en) * 2017-08-31 2021-09-01 旭化成株式会社 Composite sound absorbing material

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2514193B2 (en) * 1986-12-26 1996-07-10 旭化成工業株式会社 Moldable laminated sheet
JP2557864B2 (en) * 1986-12-26 1996-11-27 旭化成工業株式会社 Molding laminate sheet and manufacturing method thereof
JP2890203B2 (en) * 1989-11-17 1999-05-10 共和レザー株式会社 Manufacturing method of foam decorative material
JPH0516964U (en) * 1991-08-26 1993-03-02 東レ株式会社 Indoor and outdoor decorative material fastening sheet
JP2001341251A (en) * 2000-06-02 2001-12-11 Lonseal Corp Interior materials
JP2002069859A (en) * 2000-09-01 2002-03-08 Dainippon Printing Co Ltd Decorative sheet
EP1829603B1 (en) * 2004-12-21 2010-06-16 Asahi Kasei Fibers Corporation Separation-membrane support
JP2007247079A (en) * 2006-03-14 2007-09-27 Toyobo Co Ltd Laminated nonwoven fabric and synthetic leather using the same

Also Published As

Publication number Publication date
JP2011121192A (en) 2011-06-23

Similar Documents

Publication Publication Date Title
JP5272315B2 (en) Nonwoven fabric and underlay material comprising the nonwoven fabric
US9248314B2 (en) Perforated nonslip non-adhesive surface covering
KR102146642B1 (en) Nonwoven fiber sheet, method for producing same, and filter
JP7462748B2 (en) Composite sound absorbing material
JP2010128005A (en) Composite sound absorbing material
JP5788193B2 (en) Nonwoven tape base material
US20070110980A1 (en) Gypsum board liner providing improved combination of wet adhesion and strength
JP5486283B2 (en) Base material for foamed resin laminate sheet
CN105143546A (en) Resin-coated non-woven fabric
JP5697421B2 (en) Durable printing substrate
JP7802060B2 (en) Nonwoven fabric, its manufacturing method and building material
JP2004011150A (en) Wall covering material and method of manufacture the same
JP4782451B2 (en) Method for producing breathable wallpaper
JP3818129B2 (en) Wall covering material and manufacturing method thereof
JPWO2019230837A1 (en) Non-woven fabric for curtains and its manufacturing method
WO2019230836A1 (en) Wall material nonwoven fabric and method of manufacturing same
JP2019098603A (en) Wall covering material
JP3941458B2 (en) Wall covering material and manufacturing method thereof
JP2010125799A (en) Print performance functional paper
JP2022135554A (en) Sound insulating sheet and soundproof sheet
JP2008174882A (en) Woven fabric wall paper
KR20220042001A (en) Eco-friendly foaming wallpaper and method for preparing the same
JP4197766B2 (en) Non-halogen flooring
JPH0310037Y2 (en)
JP4779367B2 (en) wallpaper

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20121121

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20130809

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20130820

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20131015

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20140218

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20140221

R150 Certificate of patent or registration of utility model

Ref document number: 5486283

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R150

S111 Request for change of ownership or part of ownership

Free format text: JAPANESE INTERMEDIATE CODE: R313111

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

S531 Written request for registration of change of domicile

Free format text: JAPANESE INTERMEDIATE CODE: R313531

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

S111 Request for change of ownership or part of ownership

Free format text: JAPANESE INTERMEDIATE CODE: R313111

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250