JPH04209770A - Porous material and its production - Google Patents

Porous material and its production

Info

Publication number
JPH04209770A
JPH04209770A JP33842990A JP33842990A JPH04209770A JP H04209770 A JPH04209770 A JP H04209770A JP 33842990 A JP33842990 A JP 33842990A JP 33842990 A JP33842990 A JP 33842990A JP H04209770 A JPH04209770 A JP H04209770A
Authority
JP
Japan
Prior art keywords
porous material
powder
fine powder
fine
less
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP33842990A
Other languages
Japanese (ja)
Inventor
Koji Motoi
孝治 本居
Yosuke Tajima
陽介 田島
Katsufumi Matsumoto
松本 勝文
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.)
Sekisui Chemical Co Ltd
Original Assignee
Sekisui Chemical Co Ltd
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 Sekisui Chemical Co Ltd filed Critical Sekisui Chemical Co Ltd
Priority to JP33842990A priority Critical patent/JPH04209770A/en
Publication of JPH04209770A publication Critical patent/JPH04209770A/en
Pending legal-status Critical Current

Links

Landscapes

  • Floor Finish (AREA)

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】[Detailed description of the invention] 【産業上の利用分野】[Industrial application field]

本発明は建築材料、たとえば水に濡れやすい場所に使用
されるフロア−材、吸放湿壁材、防音材等の各種建材に
適する多孔性材料とその製造方法に関する。
The present invention relates to a porous material suitable for various building materials such as flooring materials, moisture absorbing/releasing wall materials, soundproofing materials, etc. used in places easily exposed to water, and a method for manufacturing the same.

【従来の技術】[Conventional technology]

従来から水に濡れやすい浴室、調理室、便所、玄関、ベ
ランダ、プールサイド、シャワールーム等の場所では、
水により滑ったりすることがないように、たとえば、実
公昭57−15308号公報にみられるような多孔性の
フロア−材が使用されている。 この多孔性のフロア−材は、0.3 mm以上の粒径の
砂等の骨材表面を熱硬化性樹脂で被覆し、この熱硬化性
樹脂によって骨材の接触部で連結固化されることによっ
て、骨材間に連続した透水孔が形成されていて、この透
水孔によって、水を表面から裏面部へ透過させることが
でき、水濡れ時の滑りを防止するようにしていた。
Places that are prone to getting wet, such as bathrooms, galleys, toilets, entrances, balconies, poolside, shower rooms, etc.
In order to prevent slipping due to water, a porous floor material is used, for example, as seen in Japanese Utility Model Publication No. 15308/1983. This porous floor material is made by coating the surface of aggregate such as sand with a particle size of 0.3 mm or more with thermosetting resin, and connecting and solidifying the aggregate at the contact area with this thermosetting resin. Continuous water permeable holes are formed between the aggregates, and these water permeable holes allow water to permeate from the surface to the back surface, thereby preventing slippage when wet.

【発明が解決しようとする課題】[Problem to be solved by the invention]

しかし、上記多孔性のフロア−材は、単に骨材の接触部
で連結固化して骨材間に間隙を形成しているため透水孔
の孔径が大きい。したがって、透水孔内に水とともに固
体の夾雑物が入り、目詰まりを起こして汚れやすいとい
う問題点を有していた。 本発明は、かかる従来技術の有する問題点を解決するこ
とができる新規な多孔性材料とその製造を提供すること
を目的としている。
However, in the above-mentioned porous floor material, the diameter of the water permeable pores is large because the aggregates are simply connected and solidified at the contact portions to form gaps between the aggregates. Therefore, there is a problem in that solid impurities enter the water permeation hole together with water, causing clogging and staining. An object of the present invention is to provide a novel porous material and its production that can solve the problems of the prior art.

【課題を解決するための手段】[Means to solve the problem]

このような目的を達成するために、本発明にかかる多孔
性材料は、微細粉粒体が反応性樹脂を介してその表面が
略平滑になるように加圧加熱成形されていて、前記表面
に微細な開口を有し、表面に圧力が加わったとき、表面
を濡らしている水分が前記開口を介して逃げ込む細孔が
その内部に形成されている多孔性材料であって、全細孔
容積の気孔率が2%以上であることを特徴とし、本発明
にかかる多孔性材料の製造方法は、予め粒径0.3■以
下の微細粉粒体に混合時に液状である反応性樹脂を真体
積比率でl:lから20=1の範囲で混合させて、直径
を実質的に微細粉粒体の粒径以上で5n+m以下とした
粉状体を得たのち、この粉状体を成形型上に敷き詰め、
弾性変形及び/または塑性変形可能なクッションシート
を介した状態で加圧加熱成形することを特徴としている
In order to achieve such an object, the porous material according to the present invention is a porous material in which fine powder is pressurized and heated through a reactive resin so that its surface becomes substantially smooth, and the surface is A porous material that has minute openings and has pores formed inside of it through which moisture wetting the surface escapes through the openings when pressure is applied to the surface, and the total pore volume is The method for producing a porous material according to the present invention, which is characterized by a porosity of 2% or more, involves adding a reactive resin, which is liquid at the time of mixing, to a fine powder having a particle size of 0.3 mm or less in true volume in advance. After mixing in a ratio of l:l to 20=1 to obtain a powder whose diameter is substantially greater than the particle size of the fine powder and 5n+m or less, this powder is placed on a mold. Spread it all over the
It is characterized by being pressurized and heated through a cushion sheet that can be elastically and/or plastically deformed.

【作  用】[For production]

上記多孔性材料を、たとえば、浴室等の水に濡れる場所
のフロア材として使用した場合、表面が平滑であるので
、その上に裸足で立つと足の裏が床面に滑らかに密着す
るとともに、表面が水に濡れていても、足の裏で押圧さ
れた水が開口を介して細孔内に逃げ込むため、足の裏と
多孔性材料表面との間に水の膜が無くなる。なお、細孔
は裏面までは達していないので、細孔内に入り込んだ水
が裏面側へ透過することはない。さらに、開口が微細で
あるため、汚れ等が開口から細孔に入りこまないように
なっている。 一方、上記製造方法によれば、所定粒径の微細粒状体と
、この微細粒状体に対して所定量の反応性樹脂とを混合
することにより、所定の大きさの粉状体を得ることがで
きる。そして、この粉状体を型上に敷き詰め、粉状体上
方からクツションシートで覆い、均一な圧力下で微細粉
粒体間に形成された微細な空隙を残して多孔性材料に成
形でき、この成形体を硬化させるので、成形時の開孔に
ムラが無く、表面に細孔が開孔した成形体を成形できる
For example, when the above porous material is used as a floor material in a place that gets wet with water, such as a bathroom, the surface is smooth, so when you stand barefoot on it, the soles of your feet will adhere smoothly to the floor surface. Even if the surface is wet with water, the water pressed by the sole of the foot escapes into the pores through the openings, so there is no water film between the sole of the foot and the surface of the porous material. Note that since the pores do not reach the back surface, water that has entered the pores does not permeate to the back surface side. Furthermore, since the openings are minute, dirt and the like are prevented from entering the pores through the openings. On the other hand, according to the above manufacturing method, a powder of a predetermined size can be obtained by mixing fine particles of a predetermined particle size and a predetermined amount of reactive resin with respect to the fine particles. can. Then, the powder is spread over a mold, covered with a cushion sheet from above, and molded into a porous material under uniform pressure, leaving fine voids formed between the fine powder. Since this molded body is cured, there is no unevenness in the openings during molding, and a molded body with pores formed on the surface can be molded.

【実 施 例】【Example】

以下に、本発明を、その実施例を参照しつつ詳しく説明
する。 第1図は本発明にかかる多孔性材料の1実施例を斜め上
から見た拡大断面図である。 図にみるように、この多孔性材料1は、板状になってい
て、その表面が略平滑になっている。 また、内部には、微小な細孔2が多数形成されている。 しかも、この細孔2は、表面の微小な開口3を介して外
部と連通している。 図中、4は微細粉粒体である。すなわち、細孔2はこの
微細粉粒体4と微細粉粒体4と間に形成されている。 本発明における気孔率とは、細孔2の全容積の、多孔性
材料の見掛は体積に対する容積分率であり、水銀圧入法
(150,crm相当圧から約0.01犀相当圧までの
測定範囲)により測定した細孔容積から算出したものを
言う。 すなわち、かかる気孔率が2%未満であると、水の逃げ
場が少なく、水濡れ時の防滑性に問題が出てくるため、
本発明においては2%以上であることを必要とする。 また、径がlOI!rn以上の開口3を有する細孔2の
好ましい割合は、上記水銀圧入法による全細孔容積中の
容積分率であられして35%未満、より好ましくは30
%未満である。すなわち、l10Ir以上のものが35
%以上になると、耐汚染性の点で問題がでてくる。 本発明にかかる多孔性材料は、以下のようにして製造さ
れる。 ■ 0.3mm(通常は平均値)以下の粒径を有する微
細粉粒体に、常温で液状を示す反応性樹脂を真体積比で
1:1〜20:l、好ましくはlO:3〜20:lの割
合で加えて混合する。 混合により、微細粉粒体が粉砕されてさらに微小の粉状
体になったり、樹脂の粘度や表面張力等の、界面の物理
化学的性質により、微細粉粒体および樹脂が凝集して微
細粉粒体より大きな凝集塊状の粉状体となるが、混合方
法を選択することによって、実質的に微細粉粒体の径以
上で5mm以下(粉砕により微小粉粒体の割合が10重
量%以下、5mmより大きい混合物が5重量%)の粉状
体を形成する。 混合方法としては、各種ブレンダー〔たとえば、スーパ
ーミキサー、アイリッヒミキサー(アイリッヒミキサー
社製)等〕で混合し、さらに分散機〔たとえば、ホソカ
ワミクロン社製タービュライザー、Bachoten社
製ダイノーミル等〕を用いる方法、微細粉粒体に液状樹
脂を噴霧し撹拌する装置〔たとえば、Sugie社製シ
ュギーミキサー、各種気流混合機、Acme社製サター
すミキサー、粉研パウテックス社製フローシェドミキサ
ー等〕を用いる方法等が挙げられる。 微細粉粒体としては、例えば、カオリン、クレー、ケイ
砂、天然鉱物繊維、天然石粉砕粉、マイカ、ガラスミル
ドファイバー、アルミナ短繊維、チタン酸カリウム短繊
維、カーボン短繊維、ウィスカ等が挙げられる。これら
はいずれのものも−種のみで、又は二種以上−緒に使用
することができる。 微細粉粒体の寸法・粒径は、多孔性材料の用途等によっ
て最適の寸法は変わるが粒径300um以下(なお、粒
径は揃っていることが好ましいが、 。 平均300−以下で構わない)のものが用いられる。そ
して微細粉粒体の繊維太さ、粒径、形状および熱硬化性
樹脂の粘度を調整することにより、表面開口の径を調整
することが可能である。 また、反応性樹脂としては、常温で液状物、たとえば、
不飽和ポリエステル樹脂、エポキシ樹脂、フェノール樹
脂、フラン樹脂、イミド樹脂、アクリル系樹脂(また必
ずしも加熱する必要のない常温硬化反応性樹脂を含む)
等が挙げられる。 ■ 得られた粉状体を成形型上に敷き詰める。 ■ 成形型上に均一に敷き詰めた粉状体の上から弾性変
形および/または組成変形可能なクッションシートで覆
い、このクツションシート越しに加圧するとともに、加
熱するか、加圧して賦形後加熱反応固化させて多孔性材
料を得ることができる。 上記クツションシートとしては、特に限定されないが、
たとえば、ゴムシート、フオーム、フェルト、不織布、
粘土状ペーストおよびそれらの複合物等が挙げられる。 (実施例1) 予め、カーボンミルドファイバー(平均繊維径30I!
m)2000重量部にエポキシ樹脂(油化シェル製エピ
コート828と酸無水物系硬化剤をエポキシ等量分混合
した物)2000重量部(かさ体積比1:0.30)を
加え、不二パウダル社製スパルタンリユーザーにより、
混合分散させて得た粉状体を成形型上に均質に敷き詰め
、厚み20+nmの羊毛フェルトを介して、常温でプレ
ス成形機で賦形後加熱硬化させて板状の成形体を得た。 なお、上記粉状体は、50I!m以上2mm以下の粒径
のものが98%であった。 また、全細孔容積の気孔率は6%、10如以上の細孔は
、全細孔容積の20%未満であった。 (実施例2) 予め、大理石粉砕粉(240メツシユパス)4000重
量部にビニルエステル系樹脂(日本ユピカ製)を800
重量部(かさ体積比1:0.27)を加え、アイリッヒ
ミキサー(アイリッヒミキサー社製)で混合し、さらに
ホソカワミクロン社製タービュライザーで分散させて粉
状体を得た。この粉状体を、成形型上に敷き詰め、さら
にその上に粘土状ペーストを2画に造粒し敷き詰め、加
圧硬化させて板状の成形体を得た。なお、上記粉状体は
100−以上3mm以下の粒径のものが98%であった
。 また、全細孔容積の気孔率は4%、lO−以上の細孔は
、全細孔容積の10%未満であった。 (実施例3) 白マイカ粉末(200メツシユパス)4000重量部に
スチレンモノマーを用いてlポイズに調整した不飽和ポ
リエステル樹脂1500重量部(かさ体積比1:o、2
5)を加え、粉研パウテックス社製フローシェドミキサ
ーにより混合し、成形型上に均質に敷き詰め、ウレタン
ゴムで覆い、プレス機で加圧(50kg/crt) し
た後、80℃で加熱硬化させて板状の成形体を得た。 また、全細孔容積の気孔率は4%、lOjrm以上の細
孔は、全細孔容積の5%未満であった。 (比較例1) 不二パウダル社製スパルタンリユーザーにより、混合分
散させる代わりに、アイリッヒミキサーで混合して直径
5mm以上の粉状体が10%あった以外は、実施例1と
同様にして板状の成形体を得た。 (比較例2) アイリッヒミキサーのみで混合して直径5mm以上の粉
状体が20%あった以外は、実施例2と同様にして板状
の成形体を得た。 (比較例3) 粉研パウテックス社製フローシェドミキサーにより混合
する代わりに、アイリッヒミキサーで混合して直径5m
m以上の粉状体が15%あった以外は、実施例3と同様
にして板状の成形体を得た。 (比較例4) 粉研パウテックス社製フローシェドミキサーにより混合
する代わりに、ニーダ−混線後、スーパーミキサーで混
合し、元のマイカ粉の1/2の粒径の粉状体が35%あ
った以外は、実施例3と同様にして板状の成形体を得た
。 (比較例5) 羊毛シートを用いなかった以外は、実施例1と同様にし
て成形体を得ようとした。しかし、均一な成形体が得ら
れなかった。 (従来例) 実公昭57−15308号公報に記載されたように、0
.3mm以上の粒径の砂5重量部に不飽和ポリエステル
樹脂1重量部を混合して砂の表面を樹脂で被覆し、これ
を成形型に敷き詰め80℃で加熱硬化して板状の成形体
(透水性レジンコンクリート材)を得た。 上記実施例1〜3、比較例1〜4、従来例で得られた成
形体、および、参考例としての伊勢化学製ガラスフィル
ター(孔径0.3trrnのマイクロポーラスガラス1
mmX 100mmX I OO+nm)について、開
口径、細孔容積、耐汚染性、滑り抵抗性のそれぞれの評
価を行い、その結果を第1表に示した。 なお、開口径については、水銀圧入法により測定し、そ
の評価は、全細孔容積中の容積分率が、l〇−以上が1
0%未満のものは◎で、1Oln11以上が10%以上
30%未満のものは○で、10trm以上が30%以上
あるものは×で示した。 細孔容積については、全細孔容積の気孔率が2%以上の
ものは◎で示し、2%未満のものは×で示した。 耐汚染性については、タルク粉(101!m以下)を水
中に分散させ(0,2g/cc) 、この液50ccを
試験片10100mmX100に適時散布して試験し、
その評価は、タルク粉が表面に残り、後で洗い流すこと
が可能なものは◎で、タルク粉が裏面より液出又は目詰
まりを起こしたものは×で示した。 また、滑り抵抗性については、多孔性材料の傾斜面にお
いて、第2図にみるように、JIS A3721の滑り
試験におけるフェルトの代わりに人工皮革片(50nu
nX 30mm) 5、荷重2kgを用いて、多孔性材
料(成形体)1の傾斜を変えて人工皮革片が滑り出す角
度θを測定し、摩擦係数(tanθ)を計算して求め、
その評価は摩擦係数0.6以上を◎で、0.6未満のも
のはXで示した。 第1表 第1表にみるように、実施例1〜3のものは、全て良好
であったが、比較例1〜4、従来例、参考例のものは、
耐汚染性、滑り抵抗性の何れかに問題があった。
The present invention will be explained in detail below with reference to examples thereof. FIG. 1 is an enlarged sectional view of one embodiment of the porous material according to the present invention, viewed obliquely from above. As shown in the figure, this porous material 1 is plate-shaped and has a substantially smooth surface. Moreover, a large number of minute pores 2 are formed inside. Moreover, this pore 2 communicates with the outside via a minute opening 3 on the surface. In the figure, 4 is a fine powder. That is, the pores 2 are formed between the fine powder particles 4 and the fine powder particles 4. The porosity in the present invention is the volume fraction of the total volume of the pores 2 to the apparent volume of the porous material, It is calculated from the pore volume measured according to the measurement range). In other words, if the porosity is less than 2%, there will be few places for water to escape, causing problems with slip resistance when wet.
In the present invention, the content needs to be 2% or more. Also, the diameter is lOI! A preferable ratio of the pores 2 having openings 3 of rn or more is less than 35%, more preferably 30%, as a volume fraction of the total pore volume by the mercury intrusion method.
less than %. That is, more than l10Ir is 35
% or more, problems arise in terms of stain resistance. The porous material according to the present invention is manufactured as follows. ■ A reactive resin that is liquid at room temperature is added to fine powder having a particle size of 0.3 mm (usually the average value) or less in a true volume ratio of 1:1 to 20:l, preferably 1O:3 to 20:1. : Add at a ratio of 1 and mix. Due to mixing, fine powders may be crushed into even finer powders, or due to the physicochemical properties of the interface, such as the viscosity and surface tension of the resin, fine powders and resin may aggregate and become fine powders. The powder will be in the form of agglomerates that are larger than the granules, but by selecting the mixing method, the diameter of the fine powder or granules can be substantially larger than 5 mm (the proportion of the fine granules is 10% by weight or less by pulverization, The mixture is larger than 5 mm (5% by weight) to form a powder. The mixing method includes mixing with various blenders (e.g., Super Mixer, Eirich Mixer (manufactured by Eirich Mixer), etc.), and further using a dispersing machine (e.g., Turbulizer, manufactured by Hosokawa Micron, Dyno Mill, manufactured by Bachoten, etc.). A method using a device that sprays liquid resin onto fine powder and stirs it [for example, a Shugie mixer manufactured by Sugie, various air flow mixers, a Sutter mixer manufactured by Acme, a flow shed mixer manufactured by Kouken Powtex, etc.] etc. Examples of the fine powder include kaolin, clay, silica sand, natural mineral fibers, crushed natural stone powder, mica, glass milled fibers, alumina staple fibers, potassium titanate staple fibers, carbon staple fibers, and whiskers. Any of these can be used alone or in combination. The optimum size and particle size of the fine powder varies depending on the use of the porous material, etc., but the particle size is 300 um or less (although it is preferable that the particle sizes are the same, an average of 300 um or less is acceptable. ) are used. By adjusting the fiber thickness, particle size, and shape of the fine powder and the viscosity of the thermosetting resin, it is possible to adjust the diameter of the surface opening. In addition, reactive resins that are liquid at room temperature, such as
Unsaturated polyester resins, epoxy resins, phenolic resins, furan resins, imide resins, acrylic resins (including room temperature curing reactive resins that do not necessarily require heating)
etc. ■ Spread the obtained powder on the mold. ■ Cover the powder uniformly spread on the mold with a cushion sheet that can be elastically deformed and/or compositionally deformable, apply pressure through the cushion sheet, and heat it, or heat it after shaping by applying pressure. A porous material can be obtained by reaction solidification. The above-mentioned cushion sheets are not particularly limited, but include:
For example, rubber sheets, foam, felt, non-woven fabrics,
Examples include clay-like pastes and composites thereof. (Example 1) Carbon milled fiber (average fiber diameter 30I!) was prepared in advance.
m) Add 2000 parts by weight of an epoxy resin (a mixture of Epicoat 828 manufactured by Yuka Shell Co., Ltd. and an acid anhydride curing agent in equal amounts of epoxy) (bulk volume ratio 1:0.30) to 2000 parts by weight, and add Fuji Powder to 2000 parts by weight. By Spartan re-user,
The powder obtained by mixing and dispersing was spread homogeneously on a mold, shaped with a press molding machine at room temperature through wool felt with a thickness of 20+ nm, and then heated and hardened to obtain a plate-shaped molded product. In addition, the above powder is 50I! 98% of the particles had a particle size of m or more and 2 mm or less. Further, the porosity of the total pore volume was 6%, and the pores of 10 or more were less than 20% of the total pore volume. (Example 2) In advance, 800 parts by weight of vinyl ester resin (manufactured by U-Pica Japan) was added to 4000 parts by weight of crushed marble powder (240 mesh pass).
Parts by weight (bulk volume ratio 1:0.27) were added, mixed with an Eirich mixer (manufactured by Eirich Mixer), and further dispersed with a turbulizer manufactured by Hosokawa Micron to obtain a powder. This powder was spread on a mold, and on top of it, granulated clay paste was spread in two strokes, and the powder was hardened under pressure to obtain a plate-shaped molded product. Incidentally, 98% of the powdered material had a particle size of 100 mm or more and 3 mm or less. Further, the porosity of the total pore volume was 4%, and the pores of 10- or more were less than 10% of the total pore volume. (Example 3) 4000 parts by weight of white mica powder (200 mesh pass) and 1500 parts by weight of unsaturated polyester resin adjusted to 1 poise using styrene monomer (bulk volume ratio 1:o, 2
5) was added, mixed using a flow shed mixer manufactured by Konken Powtex Co., Ltd., spread uniformly on a mold, covered with urethane rubber, pressurized with a press (50 kg/crt), and then heated and cured at 80°C. A plate-shaped molded body was obtained. Further, the porosity of the total pore volume was 4%, and the pores larger than 10jrm were less than 5% of the total pore volume. (Comparative Example 1) The procedure was the same as in Example 1, except that instead of mixing and dispersing with a Spartan Reuser manufactured by Fuji Paudal Co., Ltd., the powder was mixed with an Eirich mixer and 10% of the powder had a diameter of 5 mm or more. A plate-shaped molded body was obtained. (Comparative Example 2) A plate-shaped molded product was obtained in the same manner as in Example 2, except that 20% of the powder was mixed using an Eirich mixer and had a diameter of 5 mm or more. (Comparative Example 3) Instead of mixing with a flow shed mixer manufactured by Kouken Powtex Co., Ltd., it was mixed with an Eirich mixer and a diameter of 5 m was mixed.
A plate-shaped molded product was obtained in the same manner as in Example 3, except that 15% of the powder had a particle size of m or more. (Comparative Example 4) Instead of mixing with a flow shed mixer manufactured by Kouken Powtex, it was mixed with a super mixer after mixing with a kneader, and 35% of the powder had a particle size that was 1/2 that of the original mica powder. A plate-shaped molded body was obtained in the same manner as in Example 3 except for this. (Comparative Example 5) An attempt was made to obtain a molded article in the same manner as in Example 1, except that the wool sheet was not used. However, a uniform molded product could not be obtained. (Conventional Example) As described in Utility Model Publication No. 15308/1983, 0
.. 5 parts by weight of sand with a particle size of 3 mm or more is mixed with 1 part by weight of unsaturated polyester resin, the surface of the sand is coated with the resin, this is placed in a mold, and heated and cured at 80°C to form a plate-shaped molded product ( A water-permeable resin concrete material) was obtained. The molded bodies obtained in Examples 1 to 3, Comparative Examples 1 to 4, and the conventional example, and a glass filter manufactured by Ise Chemicals (microporous glass 1 with a pore size of 0.3 trrn) as a reference example.
mmX 100mmX IOO+nm), the opening diameter, pore volume, stain resistance, and slip resistance were evaluated, and the results are shown in Table 1. The opening diameter is measured by mercury intrusion method, and the evaluation is that if the volume fraction in the total pore volume is 10- or more,
Those with less than 0% are marked ◎, those with 1Oln11 or more of 10% or more and less than 30% are marked with ○, and those with 10trm or more of 30% or more are marked with ×. Regarding the pore volume, those whose porosity of the total pore volume was 2% or more were indicated by ◎, and those whose porosity was less than 2% were indicated by ×. Contamination resistance was tested by dispersing talcum powder (101!m or less) in water (0.2 g/cc) and spraying 50 cc of this liquid on a 10100 mm x 100 test piece at appropriate times.
The evaluation was rated ◎ if talcum powder remained on the surface and could be washed away later, and × if talcum powder leaked from the back side or caused clogging. Regarding the slip resistance, as shown in Figure 2, on the sloped surface of the porous material, a piece of artificial leather (50 nu
nX 30 mm) 5. Using a load of 2 kg, change the inclination of the porous material (molded body) 1, measure the angle θ at which the artificial leather piece starts to slide, and calculate the coefficient of friction (tan θ).
In the evaluation, a coefficient of friction of 0.6 or more was marked ◎, and a coefficient of friction less than 0.6 was marked X. Table 1 As shown in Table 1, Examples 1 to 3 were all good, but Comparative Examples 1 to 4, Conventional Example, and Reference Example were
There were problems with either stain resistance or slip resistance.

【発明の効果】【Effect of the invention】

本発明にかかる多孔性材料は、以上のように構成されて
いるので、水濡れ時に滑りにくく、しかも汚れにくい。 したがって、浴室、調理室、便所、玄関、ベランダ、プ
ールサイド、シャワールーム等におけるフロア−材とし
て有効に利用できる。 また、表面に細孔が開口していることから、フロア−材
だけでなく吸放湿壁材、防音材等各種の建築材料として
も適す。 一方、本発明にかかる多孔性材料の製造方法によれば、
上記多孔性材料を精度よく製造することができる。
Since the porous material according to the present invention is configured as described above, it is resistant to slipping when wet with water and is resistant to staining. Therefore, it can be effectively used as a flooring material in bathrooms, cooking rooms, toilets, entrances, balconies, poolsides, shower rooms, etc. In addition, since the surface has pores, it is suitable not only for flooring materials but also for various building materials such as moisture-absorbing wall materials and soundproofing materials. On the other hand, according to the method for producing a porous material according to the present invention,
The above porous material can be manufactured with high precision.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は本発明にかかる多孔性材料の1実施例をあられ
す拡大断面斜視図、第2図は滑り抵抗性試験を説明する
説明図である。 1・・・多孔性材料 2・・・細孔 3・・・開口 4・・・微細粉粒体
FIG. 1 is an enlarged cross-sectional perspective view of one embodiment of the porous material according to the present invention, and FIG. 2 is an explanatory diagram illustrating a slip resistance test. 1... Porous material 2... Pores 3... Openings 4... Fine powder and granules

Claims (2)

【特許請求の範囲】[Claims] (1)微細粉粒体が反応性樹脂を介してその表面が略平
滑になるように加圧加熱成形されていて、前記表面に微
細な開口を有し、表面に圧力が加わったとき、表面を濡
らしている水分が前記開口を介して逃げ込む細孔がその
内部に形成されている多孔性材料であって、全細孔容積
の気孔率が2%以上であることを特徴とする多孔性材料
(1) A fine powder material is pressurized and heated through a reactive resin so that its surface becomes approximately smooth, and the surface has fine openings, and when pressure is applied to the surface, the surface A porous material having pores formed therein through which water wetting the water escapes through the openings, the porous material having a porosity of 2% or more of the total pore volume. .
(2)請求項第1項記載の多孔性材料を得るにあたり、
予め粒径0.3mm以下の微細粉粒体に混合時に液状で
ある反応性樹脂を真体積比率で1:1から20:1の範
囲で混合させ、直径を実質的に微細粉粒体の粒径以上で
5mm以下とした粉状体を得たのち、この粉状体を成形
型上に敷き詰め、弾性変形及び/または塑性変形可能な
クッションシートを介した状態で加圧加熱成形すること
を特徴とする多孔性材料の製造方法。
(2) In obtaining the porous material according to claim 1,
A reactive resin that is liquid at the time of mixing is mixed in advance with fine powder particles with a particle size of 0.3 mm or less at a true volume ratio in the range of 1:1 to 20:1, and the diameter is substantially reduced to the size of the particles of the fine powder particles. After obtaining a powder whose diameter is greater than or equal to 5 mm, this powder is spread over a mold and pressurized and heated through a cushion sheet that can be elastically deformed and/or plastically deformed. A method for producing a porous material.
JP33842990A 1990-11-30 1990-11-30 Porous material and its production Pending JPH04209770A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP33842990A JPH04209770A (en) 1990-11-30 1990-11-30 Porous material and its production

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP33842990A JPH04209770A (en) 1990-11-30 1990-11-30 Porous material and its production

Publications (1)

Publication Number Publication Date
JPH04209770A true JPH04209770A (en) 1992-07-31

Family

ID=18318067

Family Applications (1)

Application Number Title Priority Date Filing Date
JP33842990A Pending JPH04209770A (en) 1990-11-30 1990-11-30 Porous material and its production

Country Status (1)

Country Link
JP (1) JPH04209770A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06321654A (en) * 1993-05-19 1994-11-22 Fujimi Ceramic Kk Expanded ceramic product for bathroom and its production

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06321654A (en) * 1993-05-19 1994-11-22 Fujimi Ceramic Kk Expanded ceramic product for bathroom and its production

Similar Documents

Publication Publication Date Title
JPH04209770A (en) Porous material and its production
HUE029345T2 (en) Sound absorbing structures
JPH04209771A (en) Porous material and its production
JPH0446074A (en) Porous material
JP2940555B2 (en) Porous molded body
JP3256178B2 (en) Method of manufacturing patterned lightweight cellular concrete panel
JP2006077433A (en) Concrete surface finishing method
JPH03108527A (en) Manufacture of porous material
JP2763121B2 (en) Floor material
JPH0314864A (en) Molding composition for porous material
JPH04301438A (en) Manufacture of porous material
JPH03100029A (en) Porous board and its preparation
JP4313468B2 (en) Method for producing porous concrete molded body
JPH0313319A (en) Method of manufacturing porous molding
JPH074265Y2 (en) Permeable flooring
JP2013217033A (en) Substrate concrete surface high-pressure adjustment method, and substrate concrete floor construction method applying the same
JPH0446076A (en) Production of porous material
JPH04203158A (en) Non-slip floor material and manufacture thereof
JPH0446072A (en) Production of porous material
JPH02228337A (en) Production of porous flooring
JPH0446075A (en) Production of porous material
JPH02178461A (en) Floor material
JPH0227301B2 (en)
JP2000129813A (en) Thermal insulation sheet material and method of manufacturing the same
JPH02228336A (en) Production of porous flooring