JPH0242958B2 - - Google Patents
Info
- Publication number
- JPH0242958B2 JPH0242958B2 JP17350584A JP17350584A JPH0242958B2 JP H0242958 B2 JPH0242958 B2 JP H0242958B2 JP 17350584 A JP17350584 A JP 17350584A JP 17350584 A JP17350584 A JP 17350584A JP H0242958 B2 JPH0242958 B2 JP H0242958B2
- Authority
- JP
- Japan
- Prior art keywords
- mineral
- fibers
- fiberboard
- skin layer
- mineral fiberboard
- 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.)
- Expired
Links
- 239000011094 fiberboard Substances 0.000 claims description 43
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 43
- 239000011707 mineral Substances 0.000 claims description 43
- 239000000835 fiber Substances 0.000 claims description 42
- 239000002557 mineral fiber Substances 0.000 claims description 28
- 230000005484 gravity Effects 0.000 claims description 17
- 239000011230 binding agent Substances 0.000 claims description 11
- 239000011490 mineral wool Substances 0.000 claims description 9
- 238000010030 laminating Methods 0.000 claims 1
- 239000010410 layer Substances 0.000 description 25
- 239000002002 slurry Substances 0.000 description 13
- 229920002472 Starch Polymers 0.000 description 8
- 239000008107 starch Substances 0.000 description 8
- 235000019698 starch Nutrition 0.000 description 8
- 239000000463 material Substances 0.000 description 7
- 230000018044 dehydration Effects 0.000 description 6
- 238000006297 dehydration reaction Methods 0.000 description 6
- 239000002537 cosmetic Substances 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 239000003973 paint Substances 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 239000000758 substrate Substances 0.000 description 5
- 229920001131 Pulp (paper) Polymers 0.000 description 4
- 239000006260 foam Substances 0.000 description 4
- 239000010893 paper waste Substances 0.000 description 4
- 239000002344 surface layer Substances 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000123 paper Substances 0.000 description 3
- 239000005011 phenolic resin Substances 0.000 description 3
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000002657 fibrous material Substances 0.000 description 2
- 239000004088 foaming agent Substances 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 239000002356 single layer Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000013585 weight reducing agent Substances 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000012784 inorganic fiber Substances 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000011268 mixed slurry Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 239000010451 perlite Substances 0.000 description 1
- 235000019362 perlite Nutrition 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 125000000914 phenoxymethylpenicillanyl group Chemical group CC1(S[C@H]2N([C@H]1C(=O)*)C([C@H]2NC(COC2=CC=CC=C2)=O)=O)C 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Paper (AREA)
Description
〔産業上の利用分野〕
本発明は建築物の天井材や壁材あるいはその他
の各種パネル用材として使用される鉱物質繊維板
に関するものである。
〔従来例の構成とその問題点〕
従来、天井板等に用いられるロツクウール板は
吸音性及び断熱性を具備させるために、繊維板を
抄造する際に、スラリー濃度を低くしたり、長繊
維材料や分散剤を加える等して繊維の絡み合い自
体を疎にすることで低密度化することや、スラリ
ー中に軽量骨材を分散させておいて、鉱物質繊維
の一部を、このような軽量な骨材で代替させて軽
量化する等の工夫がなされているが、強度や表面
化粧性の点から、従来の単層構成の鉱物質繊維板
では軽量化の限界があり、比重が0.4以下の比重
の小さい板にすると、板としての形状保持はでき
ても、天井板や壁板としての強度が不足したり、
あるいは繊維が硬い無機質の繊維であるので表面
の凹凸が著しくなつて表面平滑性を損なうと共
に、サンデイング等で平滑化しても表面が疎であ
るために化粧性に劣つてしまうという問題があつ
た。
又、繊維の密度を疎にして軽量化した場合に
は、表面に空隙が多く現れてしまい、塗装仕上げ
する時には表層の空隙部に塗料が吸込まれるため
に、その吸込みムラを防止するための下塗りが必
要となる。しかも良好な塗膜を形成するには塗料
の吸込み量を考慮して多量の塗料を塗布する必要
があり、防火性が低下してしまう虞れがあつた。
さらに、塗料の吸込みが多いと、表層部が膨張
して伸びが発生し、反りが生じるという問題点が
ある。
又、塗装に代えて化粧シートを粘着する場合に
は、繊維密度を疎にした軽量な繊維板では表面に
鉱物質繊維の毛羽立ちが発生しているために、毛
羽立つた鉱物質繊維が折れ易くて化粧シートの接
着性が極めて悪いという問題点がある。
〔発明の目的〕
本発明は上記問題点に鑑みてなされたもので、
難剥離性に優れたスキン層を形成する事により、
繊維密度の低いポーラスな鉱物質繊維板の強度及
び表面性を改善して、塗装性、化粧性を良好に
し、しかも天井板や壁板として使用できる鉱物質
繊維板の軽量化の範囲を広げることのできる鉱物
質繊維板を提供するものである。
〔発明の構成〕
上記目的を達成するために本発明の鉱物質繊維
板は、ロツクウール等の鉱物質繊維を抄造してな
る比重が0.2〜0.4の鉱物質繊維板主体の表面に繊
維長が100〜2000μの鉱物質短繊維にバインダー
を2〜20%の割合で配合した緻密なスキン層を一
体に層着してなるもので、基板が軽量であるにも
かかわらず表面が平滑で毛羽立ちがなく、且つ硬
質化した比強度の大きいものである。
〔実施例の説明〕
本発明の実施例を図面について説明すると、1
はロツクウール又はスラグウールを主体としてス
ラリー濃度の調整や軽量骨材の混入、長繊維の混
入、分散剤、起泡剤等の混入等を行つて抄造、形
成された比重0.2〜0.4の鉱物質繊維板主体で、そ
の表面に鉱物質短繊維を主体とする緻密なスキン
層2を一体に層着してある。
上記スキン層2は鉱物質短繊維を主体としてバ
インダーを2〜20%の割合で配合して形成したも
ので、その繊維長は100〜2000μ、好ましくは100
〜1000μの繊維長のものが50%以上の割合を占め
るように粉砕した鉱物質短繊維を主体にして形成
される。
ここで、100〜2000μの長さのものを使用する
のは、表面平滑性だけを改善するのであれば、通
常の鉱物質繊維板の抄造に使用される10〜30mm長
さのものより短い長さのものを使用することで目
的を達成することが出来るが、鉱物質繊維は植物
質繊維等の有機質の繊維と異なつて柔軟性を欠く
ために、別々に調整したスラリーを抄造して形成
した繊維層を重ね合わせても層間における繊維同
志の絡み合いがほとんど得られず、結合力が弱く
て剥離し易くなるという新たな問題が生じるもの
であり、100〜2000μの長さに粉砕した短繊維で
あれば繊維長が極端に短くて重ね合わせ部分にい
て、上記短繊維が圧力や脱水時の水分の移動で流
動し易く、下層の鉱物質繊維主体1を構成する鉱
物質繊維の空隙部分に食い込むようにして密着し
合つて、両者の結合点が著しく増大し、該結合点
にバインダーを作用させることでその結合点を強
固に固定してスキン層の剥離が防止されるためで
ある。又、上記スキン層は短繊維を主体として形
成したものであるので、断熱性、吸音性、通気性
を有していると共に鉱物質繊維主体1とは別の抄
造装置で均一厚さのシート状に形成して層着する
ことが可能であり、厚さや密度の調整が容易に行
なえるものである。
このような鉱物質繊維板を得るには、第2図に
示すように、まずロツクウールやスラグウール等
の繊維長が4〜30mmの鉱物質繊維にスターチ等の
バインダーを適量添加してなる低密度配合スラリ
ーに必要に応じてパーライトやシラス発泡体等の
無機質軽量骨材、もしくは分散材や起泡剤、ある
いは長繊維材料等を加えて長網あるいは丸網抄造
機等により抄造して鉱物質繊維主体1となる乾燥
後の比重が0.2〜0.4のポーラスなウエツトマツト
11を形成する。このような比重の範囲の鉱物質
繊維板主体は軽量骨材を適宜割合で混合して抄造
する方法の他に抄造時の繊維スラリーの攪拌状態
や抄造速度等の条件を調整しておいて繊維間空隙
を多くして抄造することでも達成できるものであ
り、必らずしも軽量骨材を混入して形成する必要
はない。
一方、スキン層2はロツクウールやスラグウー
ル等の鉱物質繊維を粉砕して繊維長が100〜
2000μ、好ましくは100〜1000μの短繊維とし、こ
の鉱物質短繊維に2〜20%の割合でスターチや
PVA、フエノール、アクリル、アクリルスチレ
ン、石油樹脂等のバインダーを添加すると共に必
要に応じてさらに故紙パルプ等の有機質繊維の短
繊維や顔料等の着色剤あるいは炭酸カルシウム、
クレー、シリカ、炭酸マグネシウム、鉱物粉、雲
母粉、金属粉、水酸化アルミニウム、アルミナ粉
体、カーボンブラツク、ホワイトカーボン等の無
機質の粉体を適宜添加して鉱物質短繊維主体のス
ラリーとなし、このスラリーを別な抄造装置で抄
造して前記ウエツトマツト11よりも薄いウエツ
トシート12に形成して前記鉱物質繊維のウエツ
トマツト11と重ね合わせて、ロールプレス3,
4で加圧脱脱水するか、あるいは第3図に示す如
く吸引脱水5を行つた後、乾燥して鉱物質繊維板
主体1と一体化する。
尚、上記スキン層はウエツトマツトの上面に鉱
物質短繊維にバインダーを配合した高濃度スラリ
ーを層状に供給して脱水、乾燥することで設ける
こともできる。
以上のような製造方法において、鉱物質繊維板
主体1と鉱物質短繊維を主体とするスキン層2の
界面にスターチ溶液、フエノール樹脂、メラミン
樹脂等の結合剤6を塗布して両者の密着力を高め
て形成してもよい。
尚、上記スキン層2は鉱物質繊維板主体1の両
面に配して一体的に層着してもよく、この場合は
鉱物質繊維板の両面を緻密で硬質な表層に形成し
て全体の強度を向上させることが出来るものであ
り、両面が平滑で、且つ比強度の大きな鉱物質繊
維板を得られるものである。
さらに、スキン層2の表面にはトラバーチン模
様やピン孔模模様等の公知の模様を形成してもよ
く、このはあいにはスキン層が緻密であるので孔
模様がシヤープになつて化粧性に優れたものとな
る。
次に本発明の鉱物質繊維板と従来の単層構成の
鉱物質繊維板の物性の比較を表に示す。
比較例
鉱物質繊維(繊維長4〜30mm)79重量部と故紙
パルプ10重量部、無機発泡体6重量部、スターチ
4重量部のスラリーを抄造して厚さ12mm、比重
0.32の低比重の鉱物質繊維板を形成した。このも
のは、比較的軽量ではあるが、表面が疎であつて
表面平滑性に劣るものであつた。
第1実施例
鉱物質繊維(繊維長4〜30mm)95重量部とスタ
ーチ5重量部を混合攪拌したスラリーを用いて低
密度の鉱物質繊維のウエツトマツトを抄造し、そ
の表面に鉱物質繊維の粉砕短繊維(繊維長100〜
2000μ)86重量部、スターチ4重量部、フエノー
ル樹脂10重量部の組成からなるスラリーを抄造し
た薄いウエツトシートを重ね合わせて脱水、乾燥
し厚さ約0.8mmのスキン層を一体に層着した全体
の厚さが12mmで比重0.28の鉱物質繊維板を形成し
た。この時の鉱物質繊維板主体の比重は0.21であ
り、表面のスキン層の比重は1.25であつた。この
ものは、基板である繊維板主体が繊維密度を極め
て小さくして形成してあり、繊維同志の間に多く
の空隙を有しているのもかかわらず、表面が平滑
であり、且つ緻密なスキン層で被われて表面平滑
性に優れたものであつた。
第2実施例
鉱物質繊維(繊維長4〜30mm)55重量部と故紙
パルプ10重量部、無機発泡体30重量部、スターチ
4重量部のスラリーを用いて鉱物質繊維のウエツ
トマツトを抄造し、その表面に鉱物質繊維の粉砕
短繊維(繊維長200〜1000μ)80重量部、故紙パ
ルプ6重量部、スターチ4重量部、フエノール樹
脂10重量部の組成からなるスラリーを抄造した薄
いウエツトシートを重ね合わせて脱水、乾燥し厚
さ約0.6mmのスキン層を一体に層着した全体厚さ
が12mmで比重0.26の鉱物質繊維板を形成した。
尚、鉱物質繊維板主体の比重は0.21であり、表面
のスキン層の比重は1.2であつた。このものは基
板である繊維板主体に多量の無機発泡体を混入し
てきるにもかかわらず表面が平滑であり、取扱い
時に折れてしまうこともなく、強度的にも満足の
ゆくものであつた。
前記3者の物性を比較したところ、次表の結果
が得られた。
[Industrial Application Field] The present invention relates to a mineral fiberboard used as a ceiling material, wall material, or other various panel materials for buildings. [Conventional structure and problems] Conventionally, in order to provide rock wool boards used for ceiling panels, etc. with sound absorption and heat insulation properties, when making fiberboard, the slurry concentration was lowered and long fiber materials were used. It is possible to lower the density by loosening the intertwining of the fibers by adding fibers or dispersants, or by dispersing lightweight aggregates in the slurry to make some of the mineral fibers Efforts have been made to reduce weight by replacing it with aggregate, but there is a limit to weight reduction with conventional single-layer mineral fiberboard due to strength and surface cosmetics, with a specific gravity of 0.4 or less. If you use a board with a low specific gravity, it may be able to maintain its shape as a board, but it may lack strength as a ceiling board or wall board.
Another problem is that since the fibers are hard inorganic fibers, the surface becomes extremely uneven, impairing the surface smoothness, and even when smoothed by sanding or the like, the surface is sparse, resulting in poor cosmetic properties. In addition, if the density of the fibers is reduced to reduce weight, many voids will appear on the surface, and when finishing with paint, the paint will be sucked into the voids in the surface layer. Undercoating is required. Moreover, in order to form a good coating film, it is necessary to apply a large amount of paint in consideration of the amount of paint sucked in, and there is a risk that the fire retardant properties will be lowered. Furthermore, if a large amount of paint is sucked in, the surface layer expands and stretches, causing warping. Also, when applying a decorative sheet instead of painting, lightweight fiberboard with a sparse fiber density has mineral fiber fuzz on its surface, so the fluffy mineral fibers can easily break. There is a problem that the adhesiveness of the decorative sheet is extremely poor. [Object of the invention] The present invention has been made in view of the above problems, and
By forming a skin layer with excellent peelability,
To improve the strength and surface properties of a porous mineral fiberboard with a low fiber density, to improve paintability and cosmetic properties, and to expand the range of lightweight mineral fiberboards that can be used as ceiling boards and wall boards. The present invention provides a mineral fiberboard that can be used in a variety of ways. [Structure of the Invention] In order to achieve the above object, the mineral fiberboard of the present invention has a mineral fiberboard having a specific gravity of 0.2 to 0.4 made from mineral fibers such as rock wool. It is made by integrally layering a dense skin layer containing ~2000μ mineral short fibers and a binder at a ratio of 2 to 20%, and the surface is smooth and fluff-free even though the substrate is lightweight. , and is hardened and has a high specific strength. [Description of Embodiments] Embodiments of the present invention will be explained with reference to the drawings. 1
is a mineral fiber with a specific gravity of 0.2 to 0.4 that is made from rock wool or slag wool and is made by adjusting the slurry concentration, adding lightweight aggregate, long fibers, dispersing agents, foaming agents, etc. It is mainly made of a plate, and a dense skin layer 2 mainly composed of short mineral fibers is integrally layered on its surface. The skin layer 2 is formed by blending a binder at a ratio of 2 to 20% mainly with mineral short fibers, and the fiber length is 100 to 2000μ, preferably 100μ.
It is formed mainly from pulverized short mineral fibers so that more than 50% of the fibers have a fiber length of ~1000μ. Here, the reason for using a length of 100 to 2000μ is that if only the surface smoothness is to be improved, the length is shorter than the length of 10 to 30mm used for ordinary mineral fiberboard manufacturing. However, unlike organic fibers such as vegetable fibers, mineral fibers lack flexibility, so mineral fibers are formed by making slurries prepared separately. Even if the fiber layers are stacked together, there is almost no intertwining of the fibers between the layers, and a new problem arises in that the bond strength is weak and the fibers easily peel off. If so, the fiber length is extremely short and the short fibers are located in the overlapped portion, and the short fibers easily flow due to pressure or the movement of water during dehydration, and bite into the voids of the mineral fibers that constitute the mineral fiber main body 1 in the lower layer. This is because when they come into close contact with each other, the bonding points between the two significantly increase, and by applying a binder to the bonding points, the bonding points are firmly fixed and peeling of the skin layer is prevented. In addition, since the skin layer is formed mainly of short fibers, it has heat insulation, sound absorption, and air permeability, and is also formed into a sheet of uniform thickness using a paper-making device separate from the mineral fiber main body 1. It can be formed and layered, and the thickness and density can be easily adjusted. To obtain such a mineral fiberboard, first, as shown in Figure 2, a low-density fiberboard is prepared by adding an appropriate amount of a binder such as starch to mineral fibers such as rock wool or slag wool with a fiber length of 4 to 30 mm. If necessary, inorganic lightweight aggregates such as perlite and shirasu foam, dispersants, foaming agents, or long fiber materials are added to the mixed slurry, and paper is made using a fourdrinier or round net machine to produce mineral fibers. A porous wet mat 11 having a specific gravity of 0.2 to 0.4 after drying is formed as the main body 1. Mineral fiberboard with a specific gravity within this range is mainly produced by mixing lightweight aggregate in an appropriate ratio and then making the fibers by adjusting conditions such as the stirring state of the fiber slurry and the papermaking speed during papermaking. This can also be achieved by papermaking with a large number of voids, and it is not necessarily necessary to form the paper by mixing lightweight aggregate. On the other hand, the skin layer 2 is made by crushing mineral fibers such as rock wool and slag wool to a fiber length of 100~
2000μ, preferably 100 to 1000μ short fibers, and starch or 2 to 20% of these mineral short fibers are added.
In addition to adding binders such as PVA, phenol, acrylic, acrylic styrene, petroleum resin, etc., if necessary, short organic fibers such as waste paper pulp, coloring agents such as pigments, or calcium carbonate,
Inorganic powders such as clay, silica, magnesium carbonate, mineral powder, mica powder, metal powder, aluminum hydroxide, alumina powder, carbon black, and white carbon are added as appropriate to form a slurry mainly consisting of mineral short fibers. This slurry is made into a wet sheet 12 that is thinner than the wet mat 11 by using another paper making device, and is overlapped with the wet mat 11 of the mineral fibers.
After dehydration under pressure (step 4) or suction dehydration (5) as shown in FIG. 3, it is dried and integrated with the mineral fiberboard main body 1. The skin layer can also be provided by supplying a layer of a highly concentrated slurry containing short mineral fibers and a binder to the upper surface of a wet mat, followed by dehydration and drying. In the above manufacturing method, a binder 6 such as a starch solution, phenol resin, or melamine resin is applied to the interface between the mineral fiberboard main body 1 and the skin layer 2 mainly composed of mineral short fibers to improve the adhesion between the two. It may be formed by increasing the The skin layer 2 may be arranged on both sides of the mineral fiberboard main body 1 and layered integrally. In this case, both sides of the mineral fiberboard are formed into a dense and hard surface layer to form a dense and hard surface layer. It is possible to improve the strength, and it is possible to obtain a mineral fiberboard that is smooth on both sides and has a high specific strength. Furthermore, a known pattern such as a travertine pattern or a pin hole pattern may be formed on the surface of the skin layer 2. In this case, since the skin layer is dense, the hole pattern becomes sharp and cosmetic. It will be excellent. Next, a comparison of the physical properties of the mineral fiberboard of the present invention and the conventional mineral fiberboard with a single layer structure is shown in the table. Comparative example A slurry of 79 parts by weight of mineral fibers (fiber length 4 to 30 mm), 10 parts by weight of waste paper pulp, 6 parts by weight of inorganic foam, and 4 parts by weight of starch was made into a paper with a thickness of 12 mm and a specific gravity.
A mineral fiberboard with a low specific gravity of 0.32 was formed. Although this material was relatively lightweight, the surface was rough and the surface smoothness was poor. 1st Example A low-density wet mat of mineral fibers is made using a slurry made by mixing and stirring 95 parts by weight of mineral fibers (fiber length 4 to 30 mm) and 5 parts by weight of starch, and crushed mineral fibers are coated on the surface of the wet mat. Short fiber (fiber length 100~
Thin wet sheets made from a slurry with a composition of 86 parts by weight of 2000μ), 4 parts by weight of starch, and 10 parts by weight of phenolic resin are layered, dehydrated and dried, and a skin layer of about 0.8 mm thick is layered together to form a whole. A mineral fiberboard with a thickness of 12 mm and a specific gravity of 0.28 was formed. At this time, the specific gravity of the mineral fiberboard main body was 0.21, and the specific gravity of the surface skin layer was 1.25. This material is made of fiberboard, which is the substrate, with extremely low fiber density, and although there are many voids between the fibers, the surface is smooth and dense. It was covered with a skin layer and had excellent surface smoothness. Second Example A wet mat of mineral fibers was made using a slurry of 55 parts by weight of mineral fibers (fiber length 4 to 30 mm), 10 parts by weight of waste paper pulp, 30 parts by weight of inorganic foam, and 4 parts by weight of starch. A thin wet sheet made of a slurry consisting of 80 parts by weight of crushed short mineral fibers (fiber length 200 to 1000μ), 6 parts by weight of waste paper pulp, 4 parts by weight of starch, and 10 parts by weight of phenolic resin is layered on the surface. After dehydration and drying, a skin layer with a thickness of about 0.6 mm was integrally deposited to form a mineral fiberboard with a total thickness of 12 mm and a specific gravity of 0.26.
The specific gravity of the mineral fiberboard main body was 0.21, and the specific gravity of the surface skin layer was 1.2. This product had a smooth surface, did not break during handling, and was satisfactory in terms of strength, even though a large amount of inorganic foam was mixed into the fiberboard substrate. When the physical properties of the three materials were compared, the results shown in the following table were obtained.
以上のように本発明の鉱物質繊維板によれば、
湿式抄造してなる比重が0.2〜0.4の鉱物質繊維板
主体の表面に繊維長が100〜2000μの鉱物質短繊
維にバインダーを配合してなる緻密なスキン層を
一体に層着しているので基板が低密度で軽量なも
のであるにもかかわらず、表面が平滑かつ緻密に
形成されているため、サンデイング等の表面調整
処理が不要にできると共に表面が緻密で毛羽立ち
がないから塗装に際して塗料の吸込みが殆どな
く、少ない塗布量で均一な塗膜が形成できるもの
であり、基板とな鉱物質繊維板慕いに従来よりも
多くの軽量骨材を混合したり、あるいは繊維の絡
み合いを疎にして一層の多孔質化をはかつて軽量
化の範囲を広げて、従来、強度や化粧性の点から
実施困難であつた比重が0.4以下の低密度の繊維
板を用いて、天井板や壁板等としての表面性を満
足する鉱物質繊維板が得られるものである。
又、表面が平滑面であるから、化粧シートの貼
着が容易且つ確実に行なえるものである。さらに
繊維長が100〜2000μの鉱物質短繊維にバインダ
ーを配合してスキン層を形成してあるので鉱物質
繊維板主体と表面のスキン層との層間剥離が生じ
難くなり、軽量であるにもかかわらず曲げ強度及
び表面強度に優れた鉱物質繊維板が形成出来るも
のである。
As described above, according to the mineral fiberboard of the present invention,
A dense skin layer made of short mineral fibers with a fiber length of 100 to 2000μ mixed with a binder is integrally layered on the surface of a mineral fiberboard with a specific gravity of 0.2 to 0.4 that is produced by wet papermaking. Although the substrate is low-density and lightweight, the surface is smooth and dense, eliminating the need for surface conditioning treatments such as sanding. There is almost no suction, and a uniform coating film can be formed with a small amount of application.It is possible to mix more lightweight aggregate than before with the mineral fiberboard substrate, or to loosen the entanglement of fibers. In order to make the material even more porous, we have expanded the scope of weight reduction and used low-density fiberboard with a specific gravity of 0.4 or less, which was previously difficult to achieve due to strength and cosmetic issues, such as ceiling panels and wall panels. The result is a mineral fiberboard that satisfies the surface properties as described above. Furthermore, since the surface is smooth, the decorative sheet can be attached easily and reliably. Furthermore, since the skin layer is formed by blending a binder with short mineral fibers with a fiber length of 100 to 2000 μm, delamination between the main body of the mineral fiberboard and the skin layer on the surface is less likely to occur, and it is lightweight as well. Regardless, a mineral fiberboard with excellent bending strength and surface strength can be formed.
図面は本発明の実施例を示すもので、第1図は
その断面図、第2図は製造方法を示す簡略側面
図、第3図は吸引脱水を行つた場合の簡略側面図
である。
1……鉱物質繊維板主体、2……スキン層。
The drawings show an embodiment of the present invention; FIG. 1 is a sectional view thereof, FIG. 2 is a simplified side view showing the manufacturing method, and FIG. 3 is a simplified side view when suction dehydration is performed. 1... Mineral fiberboard main body, 2... Skin layer.
Claims (1)
なる比重が0.2〜0.4の鉱物質繊維板主体の表面に
繊維長が100〜2000μの鉱物質短繊維にバインダ
ーを2〜20%割合で配合した緻密なスキン層を一
体に層着してなる鉱物質繊維板。 2 スキン層は、抄き合わせによつて鉱物繊維板
主体に一体に層着されたものである特許請求の範
囲第1項記載の鉱物質繊維板。 3 スキン層が結合剤を介して鉱物質繊維板主体
に一体に層着されている特許請求の範囲第1項又
は第2項記載の鉱物質繊維板。 4 スキン層が鉱物質繊維板主体の両面に一体に
層着されている特許請求の範囲第1項ないし、第
3項のいずれかに記載の鉱物質繊維板。[Scope of Claims] 1. On the surface of a mineral fiberboard with a specific gravity of 0.2 to 0.4, which is produced by wet paper-making of mineral fibers such as rock wool, 2 to 20% of binder is applied to short mineral fibers with a fiber length of 100 to 2000μ. A mineral fiberboard made of a dense skin layer that is blended in a % ratio. 2. The mineral fiberboard according to claim 1, wherein the skin layer is integrally layered on the main body of the mineral fiberboard by laminating. 3. The mineral fiberboard according to claim 1 or 2, wherein the skin layer is integrally layered on the mineral fiberboard main body via a binder. 4. The mineral fiberboard according to any one of claims 1 to 3, wherein the skin layer is integrally layered on both sides of the mineral fiberboard main body.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17350584A JPS6155297A (en) | 1984-08-21 | 1984-08-21 | mineral fiberboard |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17350584A JPS6155297A (en) | 1984-08-21 | 1984-08-21 | mineral fiberboard |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6155297A JPS6155297A (en) | 1986-03-19 |
| JPH0242958B2 true JPH0242958B2 (en) | 1990-09-26 |
Family
ID=15961765
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP17350584A Granted JPS6155297A (en) | 1984-08-21 | 1984-08-21 | mineral fiberboard |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6155297A (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5137353B2 (en) * | 2006-07-31 | 2013-02-06 | 大建工業株式会社 | Inorganic board and method for producing the same |
| JP5137364B2 (en) * | 2006-09-15 | 2013-02-06 | 大建工業株式会社 | Inorganic board and method for producing the same |
| WO2008016011A1 (en) * | 2006-07-31 | 2008-02-07 | Daiken Corporation | Inorganic plate and method for producing the same |
| JP6021607B2 (en) * | 2012-11-20 | 2016-11-09 | 大建工業株式会社 | Eaves ceiling material |
-
1984
- 1984-08-21 JP JP17350584A patent/JPS6155297A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6155297A (en) | 1986-03-19 |
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