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JP4094939B2 - Bathroom flooring - Google Patents
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JP4094939B2 - Bathroom flooring - Google Patents

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Publication number
JP4094939B2
JP4094939B2 JP2002341947A JP2002341947A JP4094939B2 JP 4094939 B2 JP4094939 B2 JP 4094939B2 JP 2002341947 A JP2002341947 A JP 2002341947A JP 2002341947 A JP2002341947 A JP 2002341947A JP 4094939 B2 JP4094939 B2 JP 4094939B2
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Prior art keywords
hydrophilic
flooring
paint
silicon
weight
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JP2002341947A
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JP2004176329A (en
Inventor
典彦 陰山
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Yamaha Living Tech Co Ltd
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Yamaha Living Tech Co Ltd
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  • Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)

Description

【0001】
【発明の属する技術分野】
本発明は浴室用床材及びその製造方法に係り、更に詳しくは、床材表面における親水性を十分に発揮させることのできる浴室用床材に関する。
【0002】
【従来の技術】
公知の浴室用の床材としては、SMC等のFRPにより形成されたものが広く利用されるに至っている。このような床材にあっては、表面が撥水性を有するため、入浴後の湯水が水滴状に残ってしまい、表面が滑り易くなったり、水滴にカビ等が付着して表面が汚損するという問題がある。そこで、床材表面に残った湯水の速乾性を高めるため、FRPにより形成された基材の表面に、シリカ等の親水性の添加剤を含む親水性塗料(親水性塗材)を用いて親水化処理を施すことが知られている。(特許文献1参照)
【0003】
【特許文献1】
特開2000−301054号公報
【0004】
【発明が解決しようとする課題】
しかしながら、前述したように、親水性塗材を用いると、シリカの膜内での沈降や塗材内の撥水性成分等の影響により、シリカが床材表面に殆ど発現しなかった。具体的には、床材表面におけるケイ素の量が5mol%以下となり、浴室用の床材として期待する親水性能を得ることができなかった。
【0005】
そこで、本発明者は、親水性塗材の塗布量、硬化温度及び硬化時間、プライマー層の有無等の条件を変えて種々の実験を行ったところ、床材表面におけるケイ素の量を従来よりも多く発現させることができ、且つ、高い親水性能を保有できることを知見した。
【0006】
【発明の目的】
本発明は、かかる知見に基づいて案出されたものであり、その目的は、親水性塗材による親水性を十分に発揮させることができる浴室用床材を提供することにある。
【0007】
【課題を解決するための手段】
前記目的を達成するため、本発明は、樹脂製の基材の表面側に、ケイ素を含む親水性塗材を用いて親水化処理が施された浴室用床材であって、
床材表面におけるケイ素の量をEPMAで測定したときに、当該ケイ素の量が8mol%以上16.4mol%以下である、という構成を採っている。このような構成によれば、床材表面に適度なケイ素が発現しているので、当該ケイ素により床材表面の親水性を十分に発揮させることができる。また、ケイ素の量をmol%(モル百分率)で特定したので、wt%(重量百分率)で特定するよりも、ケイ素原子の数的割合を把握し易くなり、床材表面に発現するケイ素と親水性能との相関性を明確にすることが可能となる。
ここで、ケイ素の量が8mol%未満であると、期待する親水性が床材に付与され難くなる一方、ケイ素の量が30mol%を超えると、表面平滑性が著しく低下して耐汚染性能等の低下を招き、実用上問題となる
【0008】
前記親水性塗材には、シリカが添加されているのが望ましく、これにより、床材表面の親水性をより良好に保有することが可能となる。
【0009】
本発明に係る親水性塗材としては、親水性塗料と親水化剤が挙げられる。前記親水性塗料とは、水との静止接触角が50度以下となる塗膜を形成可能な塗料を意味し、アルカリシリケート類含有無機塗料、金属アルコキシド類含有無機塗料、有機無機複合化塗料、表面親水化塗料等を例示できる。ここで、有機無機複合化塗料は、アクリル、ウレタン、ポリエステル、エポキシ等の有機成分と、ケイ素等を主成分とするシリケート等の無機成分とを、ビニル基、グリシジル基、メタクリロイル基等の末端反応基を有するアルコキシシラン類(シランカップリング剤)等で複合化した塗料である。なお、表面親水化塗料は、塗料中に親水性基を有する親水化剤等を添加し、表面にSi−OH基等の親水性基を出して親水構造とする塗料である。また、前記親水化剤とは、水との静止接触角が50度以下となる薄膜を形成可能な液体を意味し、水やアルコール類を中心とした溶媒中に、アルミナ複合金属やコロイダルシリカ等の親水性物質を含有したもの等が例示でき、親水性塗料と同様、表面にSi−OH基等の親水性基を出して親水構造とするものである。
【0010】
【発明の実施の形態】
図1(A)に示されるように、本発明に係る浴室用床材10は、樹脂製の基材11に親水性塗材を用いた親水化処理が施されて構成される。親水性塗料を用いる場合には、この基材11にプライマー塗料を用いて形成されたプライマー層12と、このプライマー層12に親水性塗料を用いて形成されたトップコート層13とを備えた構成となっている。
なお、図1(B)に示されるように、プライマー層12を省略して基材11の表面11Aにトップコート層13を直接形成してもよい。
【0011】
前記基材11としては、特に限定されるものではないが、SMC等のFRP(繊維強化プラスチック)によって形成される。
【0012】
前記プライマー塗料は、公知のプライマー塗料の成分に、少なくとも親水性物質を加えた成分構成となっている。当該親水性物質は、プライマー塗料の主剤に添加されるものであって、親水性シリカ、アルミナ等の親水性材料を意味する。また、親水化剤を用いる場合には、プライマー層12を設けずに、基材11の表面に塗布する。
【0013】
なお、本明細書において、「親水性基」とは、−OH、−O−、−NHCO−、−CONH2−、−COOH、−SO3−OSO3H、−OPO(OH)2、−NH2、−NH−、−NR2等を総称した概念として用いる。
【0014】
【実施例】
以下に本発明の実施例を比較例とともに説明する。
【0015】
[実施例1]
先ず、平面サイズが600mm角となるプレス成型板から、平面サイズ300mm角のSMCからなる基材11を切り取った。前記SMCは、不飽和ポリエステル樹脂80重量部、架橋ポリスチレン系低収縮剤20重量部、水酸化アルミニウム140重量部、炭酸カルシウム60重量部、ガラス繊維(1インチ長)100重量部、硬化剤1重量部、その他着色トナー、増粘剤、内部離型剤等の添加剤5〜20重量部を配合したものを用いた。
次いで、不織布表面処理材により基材11の表面11Aを研磨する下地処理(以下、単に「下地処理」とする)を行い、表面11Aに凹凸若しくは粗面を形成した。
次に、基材11の表面11Aに対し、プライマー塗料を吹き付けてプライマー層12を設けた。この際、塗膜の厚みを約20μmとした。前記プライマー塗料としては、アクリルポリオールを主成分とする主剤80部、ヘキサメチレンジイソシアネートを主成分とする硬化剤10部、トルエン、キシレン等の混合シンナー50部の割合で配合し、添加剤として親水性シリカ粒子を主剤に対して4重量%の添加割合で添加した。
次いで、プライマー層12の上から、親水性塗料を吹き付けてトップコート層13を設けた。この際、塗膜の厚みを約30μmとした。前記親水性塗料としては、アクリルポリオールを主成分とする主剤80部、ヘキサメチレンジイソシアネートを主成分とする硬化剤20部、トルエン、キシレン等の混合シンナー60部の割合で配合し、前記主剤には、添加剤として親水性シリカ粒子と、シリコン系界面活性剤と、平均粒径が20μmのアクリルビーズとを添加した。ここで、親水性シリカ粒子の添加割合を、主剤に対して6重量%とし、シリコン系界面活性剤及びアクリルビーズの添加割合を、主剤に対してそれぞれ5重量%とした。その後、乾燥温度120℃、乾燥時間20分間の条件下で、プライマー塗料及び親水性塗料を硬化させた後、冷却して浴室用床材10が得られた。
【0016】
[実施例2]
図2に示されるように、実施例1に対し、下地処理を行わず、且つ、プライマー層12を設けずに、トップコート層13の塗膜の厚みを約40μmとした。
【0017】
[実施例3]
実施例2と同様に、下地処理を行わず、且つ、プライマー層12を設けずに、基材11の表面11Aに親水性塗料をハンドレイアップ法により塗装した。トップコート層13の塗膜の厚みを約30μmとし、硬化条件を乾燥温度50℃、乾燥時間120分間とした。
【0018】
[実施例4]
実施例4では、実施例1と同様に切り取られた平面サイズ300mm角の基材11の表面11Aに対し、親水化剤をウエスにより塗布した。この際、親水化剤の塗布量は50g/mとした。本実施例における親水化剤としては、水60〜70重量%、エチルアルコール30〜35重量%、アルミナ複合金属0.01〜1重量%、コロイダルシリカ5重量%の割合で配合したものを用いた。
その後、常温にて約24時間乾燥させて表面硬化を行い、床材10を形成した。
【0019】
[実施例5]
実施例4に対し、親水化剤及びその塗布量を変えた。すなわち、親水化剤として、水50重量%、エチルアルコール48重量%、アルミナ複合金属0.01〜1重量%、コロイダルシリカ2重量%の割合で配合したものを用い、親水性塗材の塗布量を100g/mとした。
【0020】
[比較例1]
実施例3に対し、下地処理を行った後、スプレーにより塗膜の厚みが20μmとなるプライマー層12を設けた。また、トップコート層13の塗膜の厚みを約40μmに変えた。
【0021】
[比較例2〜3]
比較例1に対し、硬化条件を乾燥温度40℃、乾燥時間180分間に変えた。また、比較例2では、下地処理を行わず、トップコート層13の塗膜の厚みを約30μmとした。比較例3では、プライマー層12を設けなかった。
【0022】
[比較例4〜5]
実施例1に対し、強制加熱を加えずに、硬化条件を、常温、乾燥時間24時間とした。比較例4では、下地処理を行わず、トップコート層13の塗膜の厚みを約40μmとした。比較例5では、プライマー層12を設けなかった。
【0023】
[比較例6]
実施例5に対し、親水性塗材の塗布量を50g/mに変えた。その他は、実施例5と略同一の条件とした。
【0024】
以上のようにして得られた各床材10に対して、親水性を確認するための実験を行い、また、床材10の表面におけるケイ素量を測定した。結果を図2に示す。
【0025】
ここで、親水性に関する実験としては、床材10を水で洗い流した直後の状態における親水性を三段階で評価したものである。すなわち、「◎」は、床材10の表面の大部分が親水性である非常に良好な評価を表し、「○」は、床材10の表面の一部が親水性となる良好な評価を表す。また、「×」は、床材10の表面が撥水性となり、期待する親水性が得られないという評価を表す。
【0026】
ケイ素量の測定は、PMAにより、加速電圧15kV、照射線径50μm、倍率150倍の条件下で行った。この際、被試験体を導電性を有する金(Au)で蒸着したので、金について補正をした。
ここで、「EPMA」とは、電子プローブX線マイクロアナライザであり、細く絞った電子線を試料表面にあてた際に発生するX線や二次電子等を検出器で測定でき、また、前記電子線を走査したり、ステージを動かしたりすることによって試料表面の二次元的な組成分布を測定することができる解析機である。
なお、特許請求の範囲を含む本明細書において、「EPMA」は、前述したものを意味し、ケイ素の量は、EPMAにより前述の条件で測定したものである。
【0027】
また、EPMAにより床材10の表面の微細観察を行った。各実施例1〜5では、アクリルビーズとシリカが多く析出しており、床材10表面の凹凸が多く確認された。一方、各比較例では、アクリルビーズやシリカがトップコート層12内に大部分若しくは完全に埋まってしまい、床材10表面の凹凸が少なかった。従って、床材10表面の凹凸も床材10の親水性能について影響を与えるものと考えられる。
【0028】
【発明の効果】
以上の実験からも明らかなように、本発明によれば、床材表面におけるケイ素の量を8mol%以上16.4mol%以下とすることで、親水性塗材による親水性を十分に発揮させることが可能になる。
【図面の簡単な説明】
【図1】 (A)及び(B)は、本発明に係る浴室用床材の層構造を示す概略断面図。
【図2】 実験条件及び実験結果を示す図表。
【符号の説明】
10・・・浴室用床材、11・・・基材、11A・・・表面、13・・・トップコート層
[0001]
BACKGROUND OF THE INVENTION
The present invention relates to a bathroom flooring and a method for producing the same, and more particularly to a bathroom flooring that can sufficiently exhibit hydrophilicity on the surface of the flooring.
[0002]
[Prior art]
As a well-known flooring material for bathrooms, those formed by FRP such as SMC have been widely used. In such a flooring, since the surface has water repellency, the hot water after bathing remains in the form of water droplets, the surface becomes slippery, or the surface is soiled by mold or the like attached to the water droplets. There's a problem. Therefore, in order to improve the quick drying property of the hot water remaining on the floor material surface, the surface of the base material formed by FRP is made hydrophilic using a hydrophilic paint (hydrophilic coating material) containing a hydrophilic additive such as silica. It is known to perform the conversion process. (See Patent Document 1)
[0003]
[Patent Document 1]
Japanese Patent Laid-Open No. 2000-301054
[Problems to be solved by the invention]
However, as described above, when a hydrophilic coating material is used, silica hardly appears on the surface of the flooring material due to sedimentation in the silica film, water repellent components in the coating material, and the like. Specifically, the amount of silicon on the floor material surface was 5 mol% or less, and the hydrophilic performance expected as a floor material for bathrooms could not be obtained.
[0005]
Therefore, the present inventor conducted various experiments by changing the conditions such as the coating amount of the hydrophilic coating material, the curing temperature and the curing time, and the presence or absence of the primer layer. It has been found that a large amount can be expressed and a high hydrophilic performance can be retained.
[0006]
OBJECT OF THE INVENTION
The present invention has been devised based on such knowledge, and an object of the present invention is to provide a bathroom flooring that can sufficiently exhibit the hydrophilicity of the hydrophilic coating material.
[0007]
[Means for Solving the Problems]
In order to achieve the above-mentioned object, the present invention is a bathroom floor material that has been subjected to a hydrophilic treatment using a hydrophilic coating material containing silicon on the surface side of a resin base material,
When the amount of silicon on the floor material surface is measured by EPMA, the amount of silicon is 8 mol% or more and 16.4 mol% or less. According to such a configuration, since appropriate silicon is expressed on the floor material surface, the hydrophilicity of the floor material surface can be sufficiently exhibited by the silicon. Moreover, since the amount of silicon is specified by mol% (mole percentage), it is easier to grasp the numerical ratio of silicon atoms than by specifying wt% (weight percentage), and silicon and hydrophilicity expressed on the flooring surface It becomes possible to clarify the correlation with the performance.
Here, when the amount of silicon is less than 8 mol%, it is difficult to impart the expected hydrophilicity to the flooring. On the other hand, when the amount of silicon exceeds 30 mol%, the surface smoothness is remarkably lowered and the stain resistance performance, etc. This is a practical problem .
[0008]
It is desirable that silica is added to the hydrophilic coating material, which makes it possible to better retain the hydrophilicity of the flooring surface.
[0009]
Examples of the hydrophilic coating material according to the present invention include a hydrophilic paint and a hydrophilizing agent. The hydrophilic paint means a paint capable of forming a coating film having a static contact angle with water of 50 degrees or less, an alkali silicate-containing inorganic paint, a metal alkoxide-containing inorganic paint, an organic-inorganic composite paint, A surface hydrophilizing paint can be exemplified. Here, the organic / inorganic composite coating is an organic component such as acrylic, urethane, polyester, and epoxy, and an inorganic component such as silicate containing silicon as a main component, and a terminal reaction such as vinyl group, glycidyl group, and methacryloyl group. It is a paint compounded with alkoxysilanes having a group (silane coupling agent) or the like. The surface-hydrophilized paint is a paint having a hydrophilic structure by adding a hydrophilic agent having a hydrophilic group or the like to the paint and outputting a hydrophilic group such as a Si-OH group on the surface. The hydrophilizing agent means a liquid capable of forming a thin film having a static contact angle with water of 50 degrees or less, and in a solvent centered on water or alcohol, alumina composite metal, colloidal silica, etc. In the same manner as the hydrophilic paint, a hydrophilic group such as a Si—OH group is formed on the surface to form a hydrophilic structure.
[0010]
DETAILED DESCRIPTION OF THE INVENTION
As shown in FIG. 1A, a bathroom floor 10 according to the present invention is configured by applying a hydrophilic treatment to a resin base 11 using a hydrophilic coating material. In the case where a hydrophilic paint is used, a structure including a primer layer 12 formed on the base material 11 using a primer paint and a topcoat layer 13 formed on the primer layer 12 using a hydrophilic paint. It has become.
As shown in FIG. 1B, the primer layer 12 may be omitted and the topcoat layer 13 may be directly formed on the surface 11A of the substrate 11.
[0011]
Although it does not specifically limit as the said base material 11, It forms with FRP (fiber reinforced plastics), such as SMC.
[0012]
The primer paint has a component structure in which at least a hydrophilic substance is added to the components of a known primer paint. The said hydrophilic substance is added to the main ingredient of a primer coating, Comprising: Hydrophilic materials, such as hydrophilic silica and an alumina, are meant. Further, when a hydrophilizing agent is used, it is applied to the surface of the substrate 11 without providing the primer layer 12.
[0013]
In this specification, “hydrophilic group” means —OH, —O—, —NHCO—, —CONH 2, —COOH, —SO 3 H , —OSO 3 H, —OPO (OH) 2. , —NH 2 , —NH—, —NR 2 and the like are used as a generic concept.
[0014]
【Example】
Examples of the present invention will be described below together with comparative examples.
[0015]
[Example 1]
First, the base material 11 made of SMC having a plane size of 300 mm square was cut from a press-molded plate having a plane size of 600 mm square. The SMC comprises 80 parts by weight of an unsaturated polyester resin, 20 parts by weight of a crosslinked polystyrene-based low shrinkage agent, 140 parts by weight of aluminum hydroxide, 60 parts by weight of calcium carbonate, 100 parts by weight of glass fiber (1 inch long), and 1 part by weight of a curing agent. Part and other additives such as colored toner, thickener, internal mold release agent and the like were used.
Next, a base treatment (hereinafter simply referred to as “base treatment”) for polishing the surface 11A of the base material 11 with a nonwoven fabric surface treatment material was performed to form irregularities or a rough surface on the surface 11A.
Next, the primer layer 12 was provided by spraying a primer paint onto the surface 11A of the substrate 11. At this time, the thickness of the coating film was about 20 μm. The primer paint is blended in a ratio of 80 parts of a main agent mainly composed of acrylic polyol, 10 parts of a curing agent mainly composed of hexamethylene diisocyanate, and 50 parts of mixed thinner such as toluene and xylene, and hydrophilic as an additive. Silica particles were added at a ratio of 4% by weight based on the main agent.
Next, a top coat layer 13 was provided by spraying a hydrophilic paint on the primer layer 12. At this time, the thickness of the coating film was about 30 μm. The hydrophilic paint is blended in a ratio of 80 parts of a main ingredient mainly composed of acrylic polyol, 20 parts of a curing agent mainly composed of hexamethylene diisocyanate, and 60 parts of a mixed thinner such as toluene and xylene. As additives, hydrophilic silica particles, silicon surfactant, and acrylic beads having an average particle diameter of 20 μm were added. Here, the addition ratio of the hydrophilic silica particles was 6% by weight with respect to the main agent, and the addition ratio of the silicon surfactant and acrylic beads was 5% by weight with respect to the main agent. Thereafter, the primer coating and the hydrophilic coating were cured under conditions of a drying temperature of 120 ° C. and a drying time of 20 minutes, and then cooled to obtain a bathroom flooring 10.
[0016]
[Example 2]
As shown in FIG. 2, with respect to Example 1, the surface treatment was not performed, and the primer layer 12 was not provided, and the thickness of the top coat layer 13 was about 40 μm.
[0017]
[Example 3]
In the same manner as in Example 2, a hydrophilic paint was applied to the surface 11A of the base material 11 by the hand lay-up method without performing the ground treatment and without providing the primer layer 12. The thickness of the top coat layer 13 was about 30 μm, and the curing conditions were a drying temperature of 50 ° C. and a drying time of 120 minutes.
[0018]
[Example 4]
In Example 4, a hydrophilizing agent was applied to the surface 11A of the substrate 11 having a plane size of 300 mm square cut out in the same manner as in Example 1 with a waste cloth. At this time, the coating amount of the hydrophilizing agent was 50 g / m 2 . As the hydrophilizing agent in the present example, a mixture of 60 to 70% by weight of water, 30 to 35% by weight of ethyl alcohol, 0.01 to 1% by weight of alumina composite metal, and 5% by weight of colloidal silica was used. .
Then, it was made to dry for about 24 hours at normal temperature, surface hardening was performed, and the flooring 10 was formed.
[0019]
[Example 5]
Compared to Example 4, the hydrophilizing agent and its coating amount were changed. That is, as a hydrophilizing agent, a coating amount of hydrophilic coating material using 50% by weight of water, 48% by weight of ethyl alcohol, 0.01 to 1% by weight of alumina composite metal, and 2% by weight of colloidal silica was used. Was 100 g / m 2 .
[0020]
[Comparative Example 1]
The primer layer 12 having a coating film thickness of 20 μm was provided by spraying after Example 3 was ground. Further, the thickness of the top coat layer 13 was changed to about 40 μm.
[0021]
[Comparative Examples 2-3]
For Comparative Example 1, the curing conditions were changed to a drying temperature of 40 ° C. and a drying time of 180 minutes. In Comparative Example 2, the base treatment was not performed, and the thickness of the top coat layer 13 was about 30 μm. In Comparative Example 3, the primer layer 12 was not provided.
[0022]
[Comparative Examples 4 to 5]
In contrast to Example 1, no forced heating was applied, and the curing conditions were normal temperature and a drying time of 24 hours. In Comparative Example 4, the surface treatment was not performed, and the thickness of the top coat layer 13 was about 40 μm. In Comparative Example 5, the primer layer 12 was not provided.
[0023]
[Comparative Example 6]
Compared to Example 5, the coating amount of the hydrophilic coating material was changed to 50 g / m 2 . The other conditions were substantially the same as in Example 5.
[0024]
For each flooring 10 obtained as described above, an experiment for confirming hydrophilicity was performed, and the silicon amount on the surface of the flooring 10 was measured. The results are shown in FIG.
[0025]
Here, as an experiment on hydrophilicity, the hydrophilicity in a state immediately after washing the flooring 10 with water is evaluated in three stages. That is, “◎” represents a very good evaluation that most of the surface of the flooring 10 is hydrophilic, and “◯” represents a good evaluation that a part of the surface of the flooring 10 becomes hydrophilic. To express. In addition, “x” represents an evaluation that the surface of the flooring 10 becomes water-repellent and the desired hydrophilicity cannot be obtained.
[0026]
Measurement of amount of silicon is by E PMA, accelerating voltage 15kV, irradiation diameter 50 [mu] m, it was carried out under the conditions of magnification 150 times. At this time, the test object was vapor-deposited with gold (Au) having conductivity, so that gold was corrected.
Here, “EPMA” is an electron probe X-ray microanalyzer, which can measure X-rays, secondary electrons, etc. generated when a finely focused electron beam is applied to the sample surface with a detector. This analyzer can measure the two-dimensional composition distribution on the sample surface by scanning an electron beam or moving a stage.
In addition, in this specification including a claim, "EPMA" means what was mentioned above, and the quantity of silicon was measured by EPMA on the above-mentioned conditions.
[0027]
Further, the surface of the flooring 10 was finely observed by EPMA. In each Example 1-5, many acrylic beads and silica precipitated, and many unevenness | corrugations on the flooring 10 surface were confirmed. On the other hand, in each comparative example, acrylic beads and silica were mostly or completely embedded in the topcoat layer 12, and the surface of the flooring 10 was less uneven. Therefore, it is considered that the unevenness on the surface of the flooring 10 also affects the hydrophilic performance of the flooring 10.
[0028]
【The invention's effect】
As is clear from the above experiments, according to the present invention, the hydrophilicity of the hydrophilic coating material is sufficiently exhibited by setting the amount of silicon on the floor material surface to 8 mol% or more and 16.4 mol% or less. It becomes possible.
[Brief description of the drawings]
1A and 1B are schematic cross-sectional views showing a layer structure of a bathroom flooring according to the present invention.
FIG. 2 is a chart showing experimental conditions and experimental results.
[Explanation of symbols]
DESCRIPTION OF SYMBOLS 10 ... Floor material for bathrooms, 11 ... Base material, 11A ... Surface, 13 ... Topcoat layer

Claims (2)

樹脂製の基材の表面側に、ケイ素を含む親水性塗材を用いて親水化処理が施された浴室用床材であって、
床材表面におけるケイ素の量をEPMAで測定したときに、当該ケイ素の量が8mol%以上16.4mol%以下であることを特徴とする浴室用床材。
On the surface side of the resin base material, a flooring for bathroom that has been subjected to a hydrophilic treatment using a hydrophilic coating material containing silicon,
A bathroom flooring characterized in that when the amount of silicon on the surface of the flooring is measured by EPMA, the amount of silicon is 8 mol% or more and 16.4 mol% or less.
前記親水化塗材には、シリカが添加されていることを特徴とする請求項1記載の浴室用床材。  The bathroom flooring according to claim 1, wherein silica is added to the hydrophilic coating material.
JP2002341947A 2002-11-26 2002-11-26 Bathroom flooring Expired - Fee Related JP4094939B2 (en)

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JP4844273B2 (en) * 2006-07-26 2011-12-28 パナソニック電工株式会社 Water-related parts
CN102011477A (en) * 2010-12-03 2011-04-13 广东盈然木业有限公司 Self-cleaning floor board

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