JPH02275784A - Production of fiber cement board - Google Patents
Production of fiber cement boardInfo
- Publication number
- JPH02275784A JPH02275784A JP9552689A JP9552689A JPH02275784A JP H02275784 A JPH02275784 A JP H02275784A JP 9552689 A JP9552689 A JP 9552689A JP 9552689 A JP9552689 A JP 9552689A JP H02275784 A JPH02275784 A JP H02275784A
- Authority
- JP
- Japan
- Prior art keywords
- cement board
- fiber cement
- curing
- board
- green
- 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
Links
- 239000004568 cement Substances 0.000 title claims abstract description 89
- 239000000835 fiber Substances 0.000 title claims abstract description 47
- 238000004519 manufacturing process Methods 0.000 title claims description 10
- 239000000839 emulsion Substances 0.000 claims abstract description 25
- 239000002002 slurry Substances 0.000 claims abstract description 13
- 238000005520 cutting process Methods 0.000 claims abstract description 4
- 239000007787 solid Substances 0.000 claims abstract description 4
- 238000000034 method Methods 0.000 claims description 7
- 239000007864 aqueous solution Substances 0.000 abstract description 6
- 230000006378 damage Effects 0.000 abstract description 6
- 239000002245 particle Substances 0.000 abstract description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 abstract 1
- 238000000465 moulding Methods 0.000 abstract 1
- 238000001723 curing Methods 0.000 description 34
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- 239000011148 porous material Substances 0.000 description 9
- 230000008961 swelling Effects 0.000 description 8
- 238000010521 absorption reaction Methods 0.000 description 7
- 238000009826 distribution Methods 0.000 description 7
- 239000011398 Portland cement Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 238000005470 impregnation Methods 0.000 description 5
- 238000010586 diagram Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 238000006703 hydration reaction Methods 0.000 description 3
- 238000010422 painting Methods 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 125000005396 acrylic acid ester group Chemical group 0.000 description 2
- 210000000988 bone and bone Anatomy 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000013007 heat curing Methods 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 230000002093 peripheral effect Effects 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 229920002978 Vinylon Polymers 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 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
- 239000010425 asbestos Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000006253 efflorescence Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 230000009746 freeze damage Effects 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- -1 pulp Substances 0.000 description 1
- 206010037844 rash Diseases 0.000 description 1
- 239000012783 reinforcing fiber Substances 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000011882 ultra-fine particle Substances 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
- C04B41/45—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
- C04B41/46—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements with organic materials
- C04B41/48—Macromolecular compounds
- C04B41/483—Polyacrylates
Abstract
Description
本発明は繊維セメントスラリーを抄造して#&維セメン
ト板を製造する方法に関する。The present invention relates to a method for manufacturing #& fiber cement board by forming fiber cement slurry.
従来より、瓦、外装材などとして繊維セメント板が広く
採用されている。M&維セメント板Aは、第1図に示す
ようにしてl!!遺される。即ち、まず繊維セメントス
ラIノー1をハチニック式ウェットマシン2により抄造
してグリーンシート3を成形し、メーキングロール4に
より巻取った後、キャリア板5にのせ、グリーンシート
3をプレス!5!6で圧縮、脱水して所定の大きさ、形
状に切断してセメント生板7を製造する(第1図(a)
(b)(c)(cl))。
次いで、セメント生板7を積載して養生角8内において
温熱養生する。温熱養生は通常40〜60°C1湿度7
0%R8以上で6〜10時間行っている。この−次養生
の後に二次養生を行っている。
二次養生は、例えば第2図に示すようにセメント生板7
をパレット9上に積載し、最上段にシート10を覆って
5日問程度自然養生している。このようにして製造され
た繊維セメント板Aは、瓦として使用する場合にはその
表面を塗装して製品としている。又、オートクレーブ養
生をして塗装し製品化する場合は、第3図に示すように
二次養生前にアクリル系塗料、その他の合成樹脂塗料に
よりオートクレーブ前塗装をして(同図(a))白華を
防止した後オートクレーブ11によりオートクレーブ養
生を施し、塗装して製品化している。Fiber cement boards have been widely used for tiles, exterior materials, etc. M&fiber cement board A is l! as shown in FIG. ! be left behind. That is, first, fiber cement slurry I No. 1 is formed into a green sheet 3 using a beech-nick type wet machine 2, and after being wound up using a making roll 4, it is placed on a carrier plate 5, and the green sheet 3 is pressed! Steps 5 and 6 compress and dehydrate the cement and cut it into a predetermined size and shape to produce green cement board 7 (Fig. 1 (a)
(b)(c)(cl)). Next, the green cement boards 7 are loaded and cured under heat within the curing angle 8. Heat curing is usually 40-60°C, humidity 7
The test was carried out for 6 to 10 hours at 0% R8 or higher. After this second curing, a second curing is performed. For example, as shown in Fig. 2, the secondary curing is carried out by
are loaded on a pallet 9, covered with a sheet 10 on the top shelf, and left to naturally cure for about 5 days. When the fiber cement board A manufactured in this manner is used as a roof tile, the surface thereof is coated and the product is made into a product. In addition, if the product is to be painted after autoclave curing, as shown in Figure 3, pre-autoclave painting is done with acrylic paint or other synthetic resin paint before the secondary curing (Figure 3 (a)). After preventing efflorescence, autoclave curing is performed in autoclave 11, and the product is painted and manufactured.
従来にあっては、二次養生において積載したセメント生
板の端面及びその近傍の小口面より水が蒸発して乾燥し
、セメントの水利反応が充分に行なわれないという問題
があった。即ち、二次養生においては、積載したセメン
ト生板の最上段にだけシートを被せていることもあって
、シートで覆われていない積載したセメント生板の外周
部の端面からの水分の蒸発は避けられず、繊維セメント
板の中央部と外周部との乾燥状態にはかなりの差が生じ
ることになる。このため、外周端部の水和反応は充分で
なく、乾燥にともなって、多数の空隙が生成し、耐凍害
性が低下するという問題があった。
本発明は上記問題点を解決するために為されたものであ
り、その目的とするところ1よ、セメント生板の外周端
部での水利反応も充分進行させることができ、空隙を充
填して耐凍害性を向上させることができる繊維セメント
板の製造方法を提供することにある。In the past, there was a problem in that during secondary curing, water evaporated from the end faces of the loaded green cement boards and the small end faces in the vicinity and dried, resulting in insufficient water utilization reaction of the cement. In other words, in the secondary curing, only the top layer of the stacked green cement boards is covered with a sheet, so the evaporation of moisture from the outer edge of the stacked green cement boards that is not covered with the sheet is reduced. Inevitably, there will be a considerable difference in dryness between the center and the outer periphery of the fiber cement board. For this reason, the hydration reaction at the outer peripheral edge is not sufficient, and as it dries, a large number of voids are formed, resulting in a problem of reduced frost damage resistance. The present invention has been made to solve the above-mentioned problems, and has the following objectives: 1. It is possible to sufficiently advance the water utilization reaction at the outer peripheral edge of green cement boards, and to fill the voids. An object of the present invention is to provide a method for manufacturing a fiber cement board that can improve frost damage resistance.
【課題を解決するための手段1
本発明の繊維セメント板の製造方法は、繊維セメントス
ラリーを抄造してグリーンシートを成形し、グリーンシ
ートを脱水させ、所定の寸法に切断してセメント生板を
形成し、次いでセメント生板に一次養生を施した後二次
養生を施すM/L維セメント板の製造方法において、二
次養生を施す曲にセメント生板にミクロデルエマルジョ
ンを含浸すせることを特徴とするものであり、この構成
により上記課題が解決されたものである。
[作用に
二次養生を施す前にセメント生板にミクロデルエマルジ
ョンを含浸させるので、二次養生において、セメント生
板の外周端部からの水の蒸発を避けることができ、水和
反応を充分進行させることができ、しかも、空隙をミク
ロデルエマルジョンにより充填して耐凍害性を向上させ
ることができるものである。
本発明において使用するセメントとしては、普通ポルト
ランドセメント、早強ポルトランドセメント、中庸ポル
トランドセメントなどの単味ポルトランドセメント、混
合ポルトランドセメント、アルミナセメント、マグネシ
アセメントなどの特殊セメント等いずれをも採用できる
。
このセメントlこつオラストナイト、マイカ、シリカ、
セビオライト等の無機骨材、石綿、パルプ、ビニロンの
ような有msi雑などの補強繊維、所望によりリグニン
スルホン酸、ホルマリン縮合物などの撥水剤その他混和
材料が配合され適量の水を加えてm維セメントスラリー
が調製される。
この繊維セメントスラリーは従来と同様にして例えば、
ハチヱック式ウェットマシンにより抄造される。
そして本発明にあっては、セメント生板の成形後の一次
養生及び/又は二次養生前にミクロデルエマルジョンを
含浸させることを必須構成要件とするものである。ミク
ロデルエマルジョンとしては、例えばアクリル酸エステ
ル系の既架橋Ni微粒子エマルノタンを挙げることがで
き、その平均粒径は0.03μであり、Tgは一23°
C,MFT(造膜温度)は0℃、伸度は400%であり
、柔軟で取り扱い易いものが好ましい。ミクロデルエマ
ルジョンはその含有水;H液中にセメント生板を浸すか
、減圧下で含浸させる。使用するミクロデルエマルジョ
ンの固形分濃度は0.05〜・50重重量であり、セメ
ント生板に含浸させる比率は1〜5重量%である。1重
量%未満であると、防水効果が乏しく耐凍害性の向上効
果が小さく、逆に5重量%を超えると不燃試験で不合格
となる恐れがある。尚、含浸率は式[(ミクロデルエマ
ルジョンを含浸したm維セメント板の重量−繊維セメン
ト板の絶乾重量)/#&維セメント板の絶乾重量×10
0(重量%)1から算出される。
例えば、湿熱養生あるいは自然養生の場合には、m維セ
メントスラリーを抄造してセメント生板を成形し、この
セメント生板にミクロデルエマルジョン水溶液を含浸さ
せた後複数枚積載し、40〜60°C170%RH以上
で6−10hrかけて一次養生する。この後、セメント
生板にミクロデルエマルジョン水溶液を含浸させ、二次
自然養生後塗装を施して繊維セメント板を製造する。オ
ートクレーブ養生の場合には繊維セメントスラリーを抄
造してセメント生板を成形し、このセメント生板にミク
ロデルエマルジョン水溶液を含浸させた後複数枚積載し
、40〜60°C170%RH以上で6〜10hrかけ
て一次養生する。この後、セメント生板にミクロデルエ
マルジョン水溶液を含浸させ、24時間以上二次自然養
生を施す。次いで昇温1hr、保持120℃以上で3
hr、降温1hrの条件でオ−トクレーブ養生を施した
後塗装して#&維セメント板を製造する。
次に、本発明の詳細な説明する。
(実施例1)
通常の方法により繊維セメントスラリーからグリーンシ
ートを成形し、グリーンシートを脱水させ、所定の寸法
に切断してセメント生板を形成した。
二次自然養生する前に積載したセメント生板をアクリル
酸エステル系低架橋超微粒子エマルジョン(平均粒子径
0.03μ)からなる水系ミクロデルエマルジョン(固
形分濃度30重量%)に30分間浸漬した(含浸率2.
2重量%)後、5日間自然養生して繊維セメント板を製
造した。
この繊維セメント板の細孔分布比、膨潤率(凍害試験A
STMC−666A法200c/sの膨潤率)、吸水率
を測定した。結果を第1表に示す。
(実施例2)
ミクロゲルエマルジョンの含浸率を3.6重量%とじ、
オートクレーブ養生を施した以外は実施例1と同様にし
て繊維セメント板を製造した。
この繊維セメント板の細孔分布比、膨潤率、吸水率を測
定した。結果を第1表に示す。
(実施例3)
ミクロデルエマルジョンの含浸率を0.4重量%とじた
以外は実施例1と同様にして繊維セメント板を製造した
。
この繊維セメント板の細孔分布比、膨潤率、吸水率を測
定した。結果をmi表に示す。
(比較例1)
ミクロゲルエマルジョンを含浸しなかった以外は実施例
1と同様にして繊維セメント板を製造した。
この繊維セメント板の細孔分布比、膨潤率、吸水率を測
定した。結果をfjS1表に示す。
(比較例2)
ミクロゲルエマルジョンを含浸しなかった以外は実施例
2と同様にして繊維セメント板を製造した。
この繊維セメント板の細孔分布比、膨潤率、吸水率を測
定した。結果を第1表に示す。
1表
実施例
比較例
0.1〜1μの
細孔径容積
(cmコ/g) 0.0247 0,0189 0
,0501 0.0652 0,0771全細孔容積
(cmコ/g) 0,0634 0,0413 0
.2292 0.2420 0.2692細孔分布比
(%)、 39.0 45.8 30.1. 2
6.9 28.6膨潤率
(%) 0.81 0,72 3.65 4.0
8 4,86吸水率
6.2 4,7 16,1 18,5 19.
6第1表の結果より、本発明の実施例にあっては細孔分
布比が比較例のものよりも大きく、膨潤率及び吸水率は
比較例のものよりも小さいことが理解される。
【発明の効果】
本発明は、繊維セメントスラリーを抄造してグリーンシ
ートを成形し、グリーンシートを脱水させ、所定の寸法
に切断してセメント生板を形成し、次いでセメント生板
に一次養生を施した後二次養生を施す繊維セメント板の
製造方法において、二次養生を施す前にセメント生板に
ミクロゲルエマルジョンを含浸させるので、二次養生に
おいて、セメント生板の外周端部からの水の蒸発を避け
ることができるものであり、従って、水和反応を充分進
行させることができ、しかも、空隙をミクロゲルエマル
ノタンにより充填して耐凍害性を向上させることができ
るものである。[Means for Solving the Problems 1] The method for manufacturing a fiber cement board of the present invention involves forming a green sheet by making fiber cement slurry, dewatering the green sheet, and cutting it into predetermined dimensions to produce a green cement board. In the manufacturing method of M/L fiber cement board in which green cement board is first cured and then second cured, the green cement board is impregnated with microdel emulsion at the time of second curing. This configuration solves the above problems. [In action, since the green cement board is impregnated with Microdel emulsion before secondary curing, water evaporation from the outer edge of the green cement board can be avoided during the secondary curing, and the hydration reaction can be sufficiently carried out. Furthermore, the microdel emulsion can be used to fill voids and improve frost damage resistance. As the cement used in the present invention, any of plain Portland cement such as ordinary Portland cement, early strength Portland cement, and medium Portland cement, special cement such as mixed Portland cement, alumina cement, and magnesia cement can be used. This cement contains olastonite, mica, silica,
Inorganic aggregates such as Seviolite, reinforcing fibers such as asbestos, pulp, organic materials such as vinylon, water repellents such as lignin sulfonic acid, formalin condensates, and other admixtures are mixed as required, and an appropriate amount of water is added. A fiber cement slurry is prepared. This fiber cement slurry is prepared in the same way as before, for example.
The paper is made using a Hatchik-style wet machine. In the present invention, it is an essential component to impregnate the green cement board with the microdel emulsion before the primary curing and/or the secondary curing after forming. As the microdel emulsion, for example, acrylic acid ester-based pre-crosslinked Ni fine particle emulnotan can be mentioned, the average particle size is 0.03μ, and the Tg is -23°.
C. MFT (film forming temperature) is 0° C., elongation is 400%, and it is preferable that it is flexible and easy to handle. Microdel emulsion is made by immersing a green cement board in its water/H solution or impregnating it under reduced pressure. The solid content concentration of the microdel emulsion used is 0.05 to 50% by weight, and the ratio of impregnation into the green cement board is 1 to 5% by weight. If it is less than 1% by weight, the waterproofing effect will be poor and the effect of improving frost damage resistance will be small, and if it exceeds 5% by weight, there is a risk of failing the nonflammability test. The impregnation rate is determined by the formula [(weight of fiber cement board impregnated with microdel emulsion - bone dry weight of fiber cement board)/# & bone dry weight of fiber cement board x 10
Calculated from 0 (weight %) 1. For example, in the case of moist heat curing or natural curing, m-fiber cement slurry is made into paper to form a green cement board, this green cement board is impregnated with an aqueous solution of Microdel emulsion, and then multiple sheets are stacked at 40 to 60°. Primary curing is performed for 6-10 hours at C170%RH or above. Thereafter, the green cement board is impregnated with an aqueous solution of Microdel emulsion, and after a second natural curing, painting is applied to produce a fiber cement board. In the case of autoclave curing, fiber cement slurry is made into a paper to form a green cement board, this green cement board is impregnated with an aqueous solution of Microdel emulsion, then multiple sheets are loaded, and heated at 40 to 60°C and 170% RH or higher for 6 to 60 minutes. Primary curing takes 10 hours. Thereafter, the raw cement board is impregnated with an aqueous solution of Microdel emulsion and subjected to secondary natural curing for 24 hours or more. Then, the temperature was raised for 1 hour and held at 120℃ or higher for 3 hours.
After curing in an autoclave under the conditions of 1 hour and temperature drop of 1 hour, a #& fiber cement board is manufactured by painting. Next, the present invention will be explained in detail. (Example 1) A green sheet was formed from fiber cement slurry by a conventional method, and the green sheet was dehydrated and cut into a predetermined size to form a green cement board. Before secondary natural curing, the loaded green cement boards were immersed for 30 minutes in an aqueous microdel emulsion (solid content concentration 30% by weight) consisting of an acrylic acid ester-based low-crosslinked ultrafine particle emulsion (average particle size 0.03μ) ( Impregnation rate 2.
2% by weight) and then naturally cured for 5 days to produce a fiber cement board. Pore distribution ratio and swelling rate (freeze damage test A) of this fiber cement board
STMC-666A method (swelling rate of 200 c/s) and water absorption rate were measured. The results are shown in Table 1. (Example 2) The impregnation rate of the microgel emulsion was set at 3.6% by weight,
A fiber cement board was manufactured in the same manner as in Example 1 except that autoclave curing was performed. The pore distribution ratio, swelling ratio, and water absorption rate of this fiber cement board were measured. The results are shown in Table 1. (Example 3) A fiber cement board was manufactured in the same manner as in Example 1 except that the impregnation rate of the microdel emulsion was 0.4% by weight. The pore distribution ratio, swelling ratio, and water absorption rate of this fiber cement board were measured. The results are shown in the mi table. (Comparative Example 1) A fiber cement board was manufactured in the same manner as in Example 1 except that it was not impregnated with the microgel emulsion. The pore distribution ratio, swelling ratio, and water absorption rate of this fiber cement board were measured. The results are shown in table fjS1. (Comparative Example 2) A fiber cement board was manufactured in the same manner as in Example 2 except that it was not impregnated with the microgel emulsion. The pore distribution ratio, swelling ratio, and water absorption rate of this fiber cement board were measured. The results are shown in Table 1. Table 1 Examples Comparative Examples Pore diameter volume of 0.1 to 1μ (cm/g) 0.0247 0,0189 0
,0501 0.0652 0,0771 Total pore volume (cm/g) 0,0634 0,0413 0
.. 2292 0.2420 0.2692 Pore distribution ratio (%), 39.0 45.8 30.1. 2
6.9 28.6 Swelling rate (%) 0.81 0.72 3.65 4.0
8 4,86 Water absorption rate 6.2 4,7 16,1 18,5 19.
6 From the results in Table 1, it is understood that the pore distribution ratio of the examples of the present invention is larger than that of the comparative example, and the swelling ratio and water absorption rate are smaller than those of the comparative example. Effects of the Invention The present invention involves forming fiber cement slurry into a green sheet, dewatering the green sheet, cutting it into predetermined dimensions to form a green cement board, and then subjecting the green cement board to primary curing. In the manufacturing method of fiber cement board, which performs secondary curing after the second curing, the green cement board is impregnated with microgel emulsion before the second curing, so that water from the outer edge of the green cement board is absorbed during the second curing. It is possible to avoid evaporation, therefore, the hydration reaction can proceed sufficiently, and moreover, the voids can be filled with the microgel emalnotane to improve frost damage resistance.
第1図(a)(b)(c)(d)(e)(f)は繊維セ
メント板の一次養生までの製造工程を示す説明図、第2
図(、)(b)は繊維セメント板の自然養生による二次
養生の工程を示す説明図、第3図し)(b)(c)は繊
維セメント板のオートクレーブ養生による二次養生の工
程を示す説明図であって、Aは繊維セメント板、1は繊
維セメントスラリー 2はハチニック式ウェットマシン
、
3はグリーンシート、
6はプレス機、
7はセメント生板、8は養生缶、1oはシート、11は
オートクレーブである。Figures 1 (a), (b), (c), (d), (e) and (f) are explanatory diagrams showing the manufacturing process up to the primary curing of fiber cement boards;
Figures (, ) and (b) are explanatory diagrams showing the process of secondary curing by natural curing of fiber cement boards, and Figure 3) (b) and (c) are explanatory diagrams showing the process of secondary curing of fiber cement boards by autoclave curing. 1 is a fiber cement board, 1 is a fiber cement slurry, 2 is a beech-nick type wet machine, 3 is a green sheet, 6 is a press machine, 7 is a raw cement board, 8 is a curing can, 1o is a sheet, 11 is an autoclave.
Claims (3)
を成形し、グリーンシートを脱水させ、所定の寸法に切
断してセメント生板を形成し、次いでセメント生板に一
次養生を施した後二次養生を施す繊維セメント板の製造
方法において、二次養生を施す前にセメント生板にミク
ロゲルエマルジョンを含浸させることを特徴とする繊維
セメント板の製造方法。(1) Paper-making fiber cement slurry to form a green sheet, dewatering the green sheet, and cutting it into predetermined dimensions to form a green cement board.The green cement board is then subjected to primary curing, followed by secondary curing. A method for producing a fiber cement board comprising: impregnating a green cement board with a microgel emulsion before performing secondary curing.
〜50重量%であることを特徴とする請求項1記載の繊
維セメント板の製造方法。(2) The solid content concentration of the microgel emulsion is 0.05
The method for manufacturing a fiber cement board according to claim 1, characterized in that the content is 50% by weight.
上浸漬させることを特徴とする繊維セメント板の製造方
法。(3) A method for producing a fiber cement board, which comprises immersing a green cement board in a microgel emulsion for 3 seconds or more.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9552689A JPH02275784A (en) | 1989-04-15 | 1989-04-15 | Production of fiber cement board |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9552689A JPH02275784A (en) | 1989-04-15 | 1989-04-15 | Production of fiber cement board |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH02275784A true JPH02275784A (en) | 1990-11-09 |
Family
ID=14139998
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP9552689A Pending JPH02275784A (en) | 1989-04-15 | 1989-04-15 | Production of fiber cement board |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH02275784A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000167480A (en) * | 1998-12-05 | 2000-06-20 | Rohm & Haas Co | Method for coating unhardened inorganic base body |
-
1989
- 1989-04-15 JP JP9552689A patent/JPH02275784A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000167480A (en) * | 1998-12-05 | 2000-06-20 | Rohm & Haas Co | Method for coating unhardened inorganic base body |
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