JPS6112873B2 - - Google Patents
Info
- Publication number
- JPS6112873B2 JPS6112873B2 JP3734877A JP3734877A JPS6112873B2 JP S6112873 B2 JPS6112873 B2 JP S6112873B2 JP 3734877 A JP3734877 A JP 3734877A JP 3734877 A JP3734877 A JP 3734877A JP S6112873 B2 JPS6112873 B2 JP S6112873B2
- Authority
- JP
- Japan
- Prior art keywords
- inorganic
- binder
- hollow spheres
- fiberboard
- fibers
- 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 21
- 239000011230 binding agent Substances 0.000 claims description 19
- 239000010410 layer Substances 0.000 claims description 16
- 239000012784 inorganic fiber Substances 0.000 claims description 14
- 239000002344 surface layer Substances 0.000 claims description 14
- 239000005011 phenolic resin Substances 0.000 claims description 5
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 2
- 238000000748 compression moulding Methods 0.000 claims description 2
- 229920001568 phenolic resin Polymers 0.000 claims description 2
- 239000000463 material Substances 0.000 description 17
- 239000000835 fiber Substances 0.000 description 15
- 238000002156 mixing Methods 0.000 description 13
- 238000000465 moulding Methods 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 7
- 239000011521 glass Substances 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 5
- 239000011490 mineral wool Substances 0.000 description 5
- 238000005452 bending Methods 0.000 description 4
- 238000005507 spraying Methods 0.000 description 3
- JZLWSRCQCPAUDP-UHFFFAOYSA-N 1,3,5-triazine-2,4,6-triamine;urea Chemical compound NC(N)=O.NC1=NC(N)=NC(N)=N1 JZLWSRCQCPAUDP-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000003232 water-soluble binding agent Substances 0.000 description 2
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 239000011491 glass wool Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
- Porous Artificial Stone Or Porous Ceramic Products (AREA)
Description
本発明は無機質繊維板に関するものであつて、
その目的とするところは軽量、強固であり、しか
も乾式製造法にて簡単かつ安価に得ることができ
る無機質繊維板を提供するにある。
従来より無機質繊維をバインダによつて接着せ
る繊維板が建築用材として市販され、実用に供さ
れており、その製造法としては湿式法と乾式法と
があるが、湿式法の場合は廃液処理工程、乾燥工
程が必要であつてコストが高くなり、乾式法の場
合は繊維の破断、座屈のために成形時に高圧を負
荷できず、そのために接着不十分であつたり、バ
インダ量を増やす必要性が生じたりする等の欠点
があつた。
本発明はかかる従来の欠点を解消せんとするも
ので、以下詳細に説明する。本発明は無機質繊維
に所望の割合で無機質の微小中空球体を配合し、
バインダにて板状に成形したものである。ここで
無機質繊維としては例えばガラス長繊維、ガラス
ウール、ロツクウール等があり、無機質の微小中
空球体としては例えばガラス或いはセラミツク質
の微小中空球体がある。またバインダとしては水
溶性又は粉末状のフエノール樹脂、レゾルシノー
ル樹脂、ユリア樹脂、ユリアーメラミン共縮合樹
脂等があるが、その他適宜のものが用いられ、特
に限定しない。更に無機質繊維と無機質微小中空
球体との混合割合は、使用する微小中空球体の密
度によつて大きく異なるが、一般には質量混合比
(繊維質量/中空球体質量)に於いて20/1〜
0.2/1まで広範囲に可能である。例えば密度が
0.3g/cm3の微小中空球体を使用する場合、質量
混合比(繊維質量/中空球体質量)は20/1〜
0.8/1の範囲、望ましくは15/1〜2/1の範
囲がよく、密度が0.7g/cm3の微小中空球体を使
用する場合は質量混合比が17/1〜0.2/1の範
囲、望ましくは10/1〜1/1の範囲がよい。ま
たバインダは特に限定しないが、フエノール樹脂
を使用する場合では繊維板の弾性も高く且つ強度
的にもすぐれている。バインダの混入割合は質量
比(バインダ質量/繊維+中空球体質量)に於い
て2/100〜15/100程度が適当であるが、無機質
繊維と無機質微小中空球体との混合比、更には繊
維径と中空球体径によつてもバインダの混入量を
適宜調整する必要がある。
本発明による無機質繊維板を製造するに当つて
は繊維径が3〜20μ程度の無機質長繊維又は短繊
維(ウール)と、球径が5〜600μ、望ましくは
10〜250μ程度の無機質微小中空球体とを上記の
範囲において混合し、水溶性又は粉末状の樹脂バ
インダを上記の範囲の量だけスプレー或いは散布
する。ここで水溶性バインダを使用する場合は、
予め繊維及び中空球体に別個にスプレーしてバイ
ンダを付着せしめたものを所望の割合に混合して
もよい。しかしてかかる混合物を所望の面積と厚
さを有する枠内に投入し、熱と圧力を負荷して圧
縮成形することにより繊維板を得る。
ここにおいて、無機質繊維板の表層と内層にお
ける無機質繊維の割合と微小中空球体の割合とは
変えるものであり、表層は内層に比べて無機質繊
維の割合を多く配合し、また内層は表層に比べて
微小中空球体の割合を多く配合するものである。
従つて、上記繊維板の製造に当たり、無機質繊維
と微小中空球体との配合割合を変えた2種の配合
材料を用意しておき、それぞれの配合材料にバイ
ンダをスプレーによつて混合して表面層用材料と
中心層用材料とを作製し、そして中心層用材料を
両表面層用材料でサンドイツチした状態で成形す
るものである。また、水溶性バインダの水溶液を
予め繊維及び中空球体に別々にスプレーしてバイ
ンダを付着せしめ、それ等を割合を変えて混合し
て表面層用材料と中心層用材料とを作製するよう
にしても良い。
本発明は上述のように無機質繊維に無機質の微
小中空球体を配合しバインダにて結合せしめたも
のであるから、乾式工法にて簡単に得ることがで
き、また圧縮成形の際に無理なく高圧をかけるこ
とが可能となる。即ち従来の無機質繊維板の場
合、繊維の破断や座屈を避けるために成形時の負
荷圧力は高々数Kg/cm2程度しか負荷できないた
め、繊維同志の接触部分も少なく、バインダも流
れず、本発明の繊維板に比べて非常に少ない接着
点で結合賦形されており、従つて強度にも自と限
界を有するものであつた。またこの場合、たとえ
繊維の破断や座屈を避ける程度の低い負荷圧力範
囲で成形したとしても、圧力を上げる程、密度が
大きくなるから、比強度としてはメリツトがな
い。しかるに本発明にあつては無機質の微小中空
球体を混入してあるから成形時の負荷圧力を10〜
30Kg/cm2程度までスムーズに無理なく上げること
が可能であり、繊維及び中空球体相互の接触箇所
が増大し、かつバインダも加圧流動するために少
量にて極めて効率的な接着を可能とできるもので
あつて、繊維板は従来のものに比べて非常に高強
度を有するものである。またこれに加えて中空球
体自体が低密度であるため、成形時に比較的高圧
を負荷してもそのためにいたずらに繊維板の密度
をあげることはなく、軽量性を損なうことなく強
度を大巾に向上せしめ得る利点がある。また、表
層は内層に比べて無機質繊維の割合が多く配合さ
れ、内層は表層に比べて微小中空球体の割合が多
く配合されて形成されているので、表層は従来の
繊維板と同様に無機質繊維の割合が多く配合され
ていて表面美麗な状態であつて化粧性に富み、中
心部は中空球体の割合が多く配合されていて軽量
となり、また断熱性に富むという利点があり、し
かも無機質繊維板は表層と内層のサンドイツチ構
造であるため強度的にも劣ることがないという利
点がある。
以下本発明を比較例及び実施例に基づいて具体
的に説明する。
〔比較例 1〕
繊維径が5〜11μのロツクウールと平均粒径が
60μ(10〜200μ)、密度が0.33g/cm3のガラスバ
ルーンを下記第1表の如き混合割合で混合し、水
溶性のフエノール樹脂溶液を質量比〔樹脂固形分
質量/(ロツクウール+ガラスバルーン)質量〕
で8/100にてスプレーによつて均一に混入し
た。
The present invention relates to an inorganic fiberboard,
The purpose is to provide an inorganic fiberboard that is lightweight and strong, and that can be easily and inexpensively obtained by a dry manufacturing method. Fibreboard, which is made by bonding inorganic fibers with binders, has been commercially available as a building material and is in practical use.There are two methods for producing it: wet and dry.The wet method involves a waste liquid treatment process. , a drying process is required, which increases costs, and in the dry method, high pressure cannot be applied during molding due to fiber breakage and buckling, resulting in insufficient adhesion and the need to increase the amount of binder. There were drawbacks such as the occurrence of The present invention aims to overcome these conventional drawbacks and will be described in detail below. The present invention blends inorganic micro hollow spheres into inorganic fibers in a desired ratio,
It is molded into a plate shape using a binder. Examples of inorganic fibers include long glass fibers, glass wool, rock wool, etc., and examples of inorganic microscopic hollow spheres include glass or ceramic microscopic hollow spheres. Further, the binder includes water-soluble or powdered phenol resin, resorcinol resin, urea resin, urea melamine cocondensation resin, etc., but other appropriate binders can be used without particular limitation. Furthermore, the mixing ratio of inorganic fibers and inorganic microscopic hollow spheres varies greatly depending on the density of the microscopic hollow spheres used, but generally the mass mixing ratio (fiber mass/hollow sphere mass) is 20/1 to 20/1.
A wide range of up to 0.2/1 is possible. For example, the density
When using micro hollow spheres of 0.3 g/ cm3 , the mass mixing ratio (fiber mass/hollow sphere mass) is 20/1 ~
The mass mixing ratio is preferably in the range of 0.8/1, preferably in the range of 15/1 to 2/1, and when using micro hollow spheres with a density of 0.7 g/cm 3 , the mass mixing ratio is in the range of 17/1 to 0.2/1. It is preferably in the range of 10/1 to 1/1. Although the binder is not particularly limited, when a phenolic resin is used, the fiberboard has high elasticity and excellent strength. The mixing ratio of the binder is approximately 2/100 to 15/100 in terms of mass ratio (binder mass/fiber + hollow sphere mass), but the mixing ratio of inorganic fibers and inorganic fine hollow spheres, and even the fiber diameter It is also necessary to adjust the amount of binder mixed depending on the diameter of the hollow sphere. In producing the inorganic fiberboard according to the present invention, inorganic long fibers or short fibers (wool) with a fiber diameter of about 3 to 20 μm and spherical diameter of 5 to 600 μm, preferably
Inorganic minute hollow spheres of about 10 to 250 microns are mixed in the above range, and a water-soluble or powdered resin binder is sprayed or dispersed in the above range. If you use a water-soluble binder here,
The binder may be applied to the fibers and the hollow spheres by spraying them separately in advance and then mixed in a desired ratio. Then, the mixture is put into a frame having a desired area and thickness, and compression molded by applying heat and pressure to obtain a fiberboard. Here, the ratio of inorganic fibers and the ratio of micro hollow spheres in the surface layer and inner layer of the inorganic fiberboard are changed, and the ratio of inorganic fibers in the surface layer is higher than that in the inner layer, and the ratio of inorganic fibers in the inner layer is higher than that in the surface layer. It contains a large proportion of micro hollow spheres.
Therefore, in manufacturing the above-mentioned fiberboard, two types of compound materials with different blending ratios of inorganic fibers and micro hollow spheres are prepared, and a binder is mixed with each compound material by spraying to form a surface layer. The material for the center layer and the material for the center layer are prepared, and the material for the center layer is sandwiched with the materials for both surface layers and then molded. Alternatively, an aqueous solution of a water-soluble binder is separately sprayed on the fibers and the hollow spheres in advance to adhere the binder, and the materials are mixed in different proportions to prepare the surface layer material and the center layer material. Also good. As described above, the present invention is made by blending inorganic microscopic hollow spheres with inorganic fibers and bonding them together with a binder, so it can be easily obtained using a dry method, and it can be easily obtained at high pressure during compression molding. It becomes possible to apply. In other words, in the case of conventional inorganic fiberboards, in order to avoid fiber breakage and buckling, the load pressure during molding can only be a few kg/ cm2 at most, so there are few contact areas between the fibers and the binder does not flow. Compared to the fiberboard of the present invention, the fiberboard is bonded and shaped with far fewer bonding points, and therefore has its own limitations in strength. In this case, even if molding is carried out in a low load pressure range that avoids fiber breakage and buckling, the density increases as the pressure increases, so there is no merit in terms of specific strength. However, in the case of the present invention, since inorganic minute hollow spheres are mixed, the load pressure during molding can be reduced to 10~10.
It is possible to raise the weight up to about 30Kg/cm 2 smoothly and without difficulty, and the contact points between the fibers and the hollow spheres are increased, and the binder also flows under pressure, making it possible to bond extremely efficiently with a small amount. The fiberboard has much higher strength than conventional fiberboard. In addition, since the hollow sphere itself has a low density, even if relatively high pressure is applied during molding, the density of the fiberboard will not increase unnecessarily, allowing for greater strength without sacrificing lightness. There are advantages that can be improved. In addition, the surface layer has a higher proportion of inorganic fibers than the inner layer, and the inner layer has a higher proportion of micro hollow spheres than the surface layer, so the surface layer is made of inorganic fibers like conventional fiberboards. It contains a high proportion of hollow spheres, giving it a beautiful surface and is highly cosmetic.The center contains a large proportion of hollow spheres, making it lightweight, and has the advantage of being highly insulating. It has the advantage of having a sandwich structure between the surface layer and the inner layer, so it is not inferior in strength. The present invention will be specifically described below based on comparative examples and examples. [Comparative Example 1] Rock wool with a fiber diameter of 5 to 11μ and an average particle diameter of
Glass balloons with a diameter of 60 μ (10 to 200 μ) and a density of 0.33 g/cm 3 are mixed at the mixing ratio shown in Table 1 below, and a water-soluble phenol resin solution is added to the mass ratio [resin solid mass/(rock wool + glass balloon)]. )mass〕
It was mixed uniformly by spraying at 8/100.
【表】【table】
比較例1と同じロツクウールとガラスバルーン
を使用し、両者の混合割合をB試料と同様にし、
バインダとしてユリアーメラミン共縮合樹脂を使
用してその混入量も質量比で8/100にした材料
を作製した。次いで成形条件を比較例1と全く同
じ条件で繊維板を成形し、曲げ強度を測定したと
ころ、B試料に比べて若干強度が落ちたが、D試
料(ガラスバルーンを混合しない場合)よりはは
るかに強化された繊維板であつた。
〔実施例〕
比較例1と同じロツクウールとガラスバルーン
を使用し、両者の混合割合を第2表の如く混合し
た2種の配合材料にフエノール樹脂溶液を同表の
量だけスプレーによつて均一に混入して表面層用
材料と中心層用材料を作製した。
The same rock wool and glass balloon as in Comparative Example 1 were used, and the mixing ratio of both was the same as in Sample B.
A material was prepared in which a urea melamine cocondensation resin was used as a binder and the amount of the mixed resin was 8/100 in terms of mass ratio. Next, a fiberboard was molded under the same molding conditions as in Comparative Example 1, and the bending strength was measured. Although the strength was slightly lower than that of sample B, it was much lower than that of sample D (when glass balloons were not mixed). It was made of reinforced fiberboard. [Example] The same rock wool and glass balloon as in Comparative Example 1 were used, and the phenol resin solution was uniformly sprayed in the amount shown in Table 2 to two types of compounded materials whose mixing ratios were as shown in Table 2. A material for the surface layer and a material for the center layer were prepared by mixing the materials.
【表】
これらの材料を用い、表裏両層が共に0.3mmに
なるように表面層用材料を使用し、中心層が0.4
mmになるように中心層用材料を使用して、成形温
度200℃、成形時間5分、成形圧力9〜15Kg/cm2
の範囲で300W×600L×10Hの寸法のサンドイツチ
状繊維板を得た。この繊維板をE試料とする。し
かしてこのE試料より試料を採取し、曲げ強度を
測定した結果を上記のB試料、D試料と対比して
第2図に示した。E試料では強度的にはB試料よ
りも若干落ちたが、表面は非常に美麗であつた。[Front] Using these materials, use the surface layer material so that both the front and back layers are 0.3 mm, and the center layer is 0.4 mm.
Use the center layer material so that the thickness is 200℃, molding temperature 200℃, molding time 5 minutes, molding pressure 9-15Kg/cm 2
Sand German trench fiberboards with dimensions of 300 W × 600 L × 10 H were obtained in the range of . This fiberboard is designated as E sample. However, a sample was taken from this sample E, and the bending strength was measured, and the results are shown in FIG. 2 in comparison with the above samples B and D. Although the strength of sample E was slightly lower than that of sample B, the surface was very beautiful.
第1図は本発明の比較例1に於ける各試料の密
度と曲げ強度との関係を示す特性図、第2図は同
上の実施例に於ける各試料の密度と曲げ強度との
関係を示す特性図である。
Figure 1 is a characteristic diagram showing the relationship between density and bending strength of each sample in Comparative Example 1 of the present invention, and Figure 2 is a characteristic diagram showing the relationship between density and bending strength of each sample in the same example. FIG.
Claims (1)
1〜0.2/1の割合で配合されてバインダにて結
合されており、表層は内層に比べて無機質繊維の
割合が多く配合され、内層は表層に比べて微小中
空球体の割合が多く配合されて形成されて成るこ
とを特徴とする無機質繊維板。 2 バインダとしてフエノール樹脂を用いたこと
を特徴とする特許請求の範囲第1項記載の無機質
繊維板。 3 製板を圧縮成形にて行つたことを特徴とする
特許請求の範囲第1項又は第2項記載の無機質繊
維板。[Claims] 1. Inorganic fibers and inorganic minute hollow spheres are 20/20/
They are blended at a ratio of 1 to 0.2/1 and bonded with a binder, with the surface layer containing a higher proportion of inorganic fibers than the inner layer, and the inner layer containing a higher proportion of micro hollow spheres than the surface layer. An inorganic fiberboard comprising: 2. The inorganic fiberboard according to claim 1, characterized in that a phenolic resin is used as the binder. 3. The inorganic fiberboard according to claim 1 or 2, characterized in that the board is made by compression molding.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3734877A JPS53121816A (en) | 1977-03-31 | 1977-03-31 | Inorganic fiber board |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3734877A JPS53121816A (en) | 1977-03-31 | 1977-03-31 | Inorganic fiber board |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS53121816A JPS53121816A (en) | 1978-10-24 |
| JPS6112873B2 true JPS6112873B2 (en) | 1986-04-10 |
Family
ID=12495058
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3734877A Granted JPS53121816A (en) | 1977-03-31 | 1977-03-31 | Inorganic fiber board |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS53121816A (en) |
-
1977
- 1977-03-31 JP JP3734877A patent/JPS53121816A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS53121816A (en) | 1978-10-24 |
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