JPH01224253A - Production of calcium silicate-polymer composite board - Google Patents
Production of calcium silicate-polymer composite boardInfo
- Publication number
- JPH01224253A JPH01224253A JP4969088A JP4969088A JPH01224253A JP H01224253 A JPH01224253 A JP H01224253A JP 4969088 A JP4969088 A JP 4969088A JP 4969088 A JP4969088 A JP 4969088A JP H01224253 A JPH01224253 A JP H01224253A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- slurry
- calcium silicate
- parts
- solid content
- 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.)
- Granted
Links
- 239000002131 composite material Substances 0.000 title claims abstract description 27
- 229920000642 polymer Polymers 0.000 title claims abstract description 23
- 238000004519 manufacturing process Methods 0.000 title claims description 17
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 title abstract description 4
- 229910052791 calcium Inorganic materials 0.000 title abstract description 4
- 239000011575 calcium Substances 0.000 title abstract description 4
- 239000002002 slurry Substances 0.000 claims abstract description 53
- 239000000378 calcium silicate Substances 0.000 claims abstract description 41
- 229910052918 calcium silicate Inorganic materials 0.000 claims abstract description 41
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 claims abstract description 41
- 229920000126 latex Polymers 0.000 claims abstract description 29
- 239000004816 latex Substances 0.000 claims abstract description 29
- 239000007787 solid Substances 0.000 claims abstract description 26
- 229920003043 Cellulose fiber Polymers 0.000 claims abstract description 17
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 claims abstract description 16
- 229920003048 styrene butadiene rubber Polymers 0.000 claims abstract description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 16
- 238000004062 sedimentation Methods 0.000 claims abstract description 14
- 239000002174 Styrene-butadiene Substances 0.000 claims abstract description 13
- 239000011115 styrene butadiene Substances 0.000 claims abstract description 13
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 12
- 125000002091 cationic group Chemical group 0.000 claims abstract description 11
- 229920006318 anionic polymer Polymers 0.000 claims abstract description 8
- 238000000034 method Methods 0.000 claims description 31
- 239000000835 fiber Substances 0.000 claims description 4
- 239000012784 inorganic fiber Substances 0.000 claims 1
- 239000000203 mixture Substances 0.000 abstract description 14
- 238000013329 compounding Methods 0.000 abstract 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 11
- 230000005484 gravity Effects 0.000 description 8
- 239000003365 glass fiber Substances 0.000 description 4
- 238000001027 hydrothermal synthesis Methods 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 3
- 125000000129 anionic group Chemical group 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 229920002401 polyacrylamide Polymers 0.000 description 3
- 235000012239 silicon dioxide Nutrition 0.000 description 3
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 2
- 239000000920 calcium hydroxide Substances 0.000 description 2
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 2
- 235000011116 calcium hydroxide Nutrition 0.000 description 2
- 239000003610 charcoal Substances 0.000 description 2
- 239000000701 coagulant Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000010451 perlite Substances 0.000 description 2
- 235000019362 perlite Nutrition 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- 229920002972 Acrylic fiber Polymers 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 229920002978 Vinylon Polymers 0.000 description 1
- UGGQKDBXXFIWJD-UHFFFAOYSA-N calcium;dihydroxy(oxo)silane;hydrate Chemical compound O.[Ca].O[Si](O)=O UGGQKDBXXFIWJD-UHFFFAOYSA-N 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000000834 fixative Substances 0.000 description 1
- 239000008394 flocculating agent Substances 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 238000007517 polishing process Methods 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
Landscapes
- Producing Shaped Articles From Materials (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は抄造法による珪酸カルシウム・ポリマー複合板
の製造方法に関し、更に詳しくは珪酸カルシウム水和物
にポリマーを定着させ丸網、長網またはフローオン式に
よる厚さ15論輸以下の軽量珪酸カルシウム・ポリマー
複合板の製造方法に関する。Detailed Description of the Invention [Industrial Application Field] The present invention relates to a method for producing a calcium silicate/polymer composite plate by a papermaking method, and more specifically, it relates to a method for producing a calcium silicate/polymer composite plate by a papermaking method, and more specifically, it relates to a method for producing a calcium silicate/polymer composite plate by fixing a polymer on a calcium silicate hydrate to form a circular wire, fourdrinier or The present invention relates to a method for producing a lightweight calcium silicate/polymer composite plate having a thickness of 15 mm or less using a flow-on method.
[従来の技術・課題]
従来、厚さ151以下の珪酸カルシウム板の製造法は抄
造法によることが一般的であり、JIS^5418にも
規定されている。この規定で示される最も嵩比重の軽い
製品は嵩比重0.8 (+0.1.−0.2)のもので
、・この嵩比重の範囲では、木材に比較して切削性に乏
しく、加工しにくいという欠点があった。また、嵩比重
をこの規定に示す範囲以下にすると、強度が弱くなり、
厚さ151以下の板状製品としての実用性が得られなか
った。[Prior Art/Problems] Conventionally, a method for manufacturing calcium silicate plates having a thickness of 151 mm or less has generally been based on a papermaking method, which is also specified in JIS^5418. The product with the lightest bulk specific gravity specified in this regulation is one with a bulk specific gravity of 0.8 (+0.1.-0.2), and within this bulk specific gravity range, it has poor cutting properties compared to wood, and it is difficult to process. The drawback was that it was difficult to do. Also, if the bulk specific gravity is lower than the range shown in this regulation, the strength will be weakened,
Practicality as a plate-like product with a thickness of 151 mm or less could not be obtained.
より軽量、高強度にするための提案として特開昭62−
138351号公報があり、JIS^5418に規定す
る製品に比べて軽重、高強度のものが得られるが、それ
でも木材に比べると靭性ば乏しく、切削・加工性に欠け
るという欠点があった。Unexamined Japanese Patent Publication No. 1983-1982 as a proposal to make it lighter and stronger
No. 138351, it is possible to obtain products that are lighter and heavier and have higher strength than the products specified in JIS^5418, but they still have the drawbacks of poor toughness and poor cutting and workability compared to wood.
この靭性改良のために、珪酸カルシウム ポリマー複合
体が考案された。この珪酸カルシウム・ポリマー複合体
は製造方法は特公昭52−39702号公報、特開昭5
2−15516号公報、特公昭62−32148号公報
等に開示されているが、これらの技術はその成形法がい
ずれもモールドブレスを基本としており、脱水を容易に
するためプレス面に金網もしくは枦布を敷くため、平滑
な表面が得られにくいことや、脱水時の水の抜は道によ
り内部に欠陥ができ易く、厚さ約15i*−以下の成形
体の製造は困難であった。To improve this toughness, a calcium silicate polymer composite was devised. The manufacturing method of this calcium silicate polymer composite is disclosed in Japanese Patent Publication No. 52-39702 and Japanese Patent Application Laid-open No. 52-39702.
These techniques are disclosed in Japanese Patent Publication No. 2-15516, Japanese Patent Publication No. 62-32148, etc., but the molding methods of these technologies are all based on mold press, and in order to facilitate dewatering, a wire mesh or mesh is placed on the press surface. Since it is spread with cloth, it is difficult to obtain a smooth surface, and the drainage during dehydration tends to cause defects inside, making it difficult to produce molded products with a thickness of about 15 i* or less.
従って、厚さ15m5以下の板状成形体を得るには、厚
さ15mm程度の成形体をいったんWJi造した後、研
摩等により所望の厚さのものを製造しているのが現状で
ある。このため、薄物製造の生産性が悪く、コスト高で
あり、且つ研摩工程を使用しても厚さ8請−以下の製品
の製造は困難であった。Therefore, in order to obtain a plate-shaped molded product with a thickness of 15 m or less, the current method is to once form a molded product with a thickness of about 15 mm using WJI, and then manufacture it to the desired thickness by polishing or the like. For this reason, the productivity of manufacturing thin products is poor, the cost is high, and even if a polishing process is used, it is difficult to manufacture products with a thickness of 8 cm or less.
また、特開昭62−52159号公報はその成形法の基
本が押出成形であり、本質的に抄造法と原理を異にする
。Furthermore, the basic molding method of JP-A-62-52159 is extrusion molding, which essentially differs in principle from the papermaking method.
従って、本発明の目的は従来の抄造法による珪酸カルシ
ウム板またはモールドブレス法による珪酸カルシウム・
ポリマー複合板の製造上及び性能上の欠点、すなわち生
産性、強度、加工性に関する問題点を改良し、軽量且つ
高強度の薄物珪酸カルシウム板を効率良(製造する方法
を提供するにある。Therefore, the object of the present invention is to produce a calcium silicate plate using the conventional papermaking method or a calcium silicate plate using the mold press method.
The purpose of the present invention is to provide a method for efficiently producing lightweight and high-strength thin calcium silicate plates by improving the production and performance disadvantages of polymer composite plates, that is, problems related to productivity, strength, and workability.
[課題を解決するための手段]
すなわち、本発明は沈降容積が10mf/9以上の珪酸
カルシウム水和Th1OO重量部、スチレンブタジェン
ラテックス3〜15重量部、枦氷炭が3’10ml以下
のセルローズ繊維をスラリー固形分の1〜5重量%、カ
チオン型のラテックス定着剤を前記スチレン・ブタジエ
ンラテックス重量の1〜20重量%及び水を調合して固
形分濃度0.5〜4重量%のスラリーを得、該スラリー
を抄造バットに注入する際に、更にアニオン型高分子凝
集剤をスラリーの固形分の20〜10000pp−の範
囲の量で滴下して抄造するこiを特徴とする珪酸カルシ
ウム・ポリマー複合板の製造方法に係る。[Means for Solving the Problems] That is, the present invention uses calcium silicate hydrated Th1OO parts by weight with a sedimentation volume of 10 mf/9 or more, 3 to 15 parts by weight of styrene-butadiene latex, and cellulose with a sedimentation volume of 3'10 ml or less. A slurry with a solid content of 1 to 5% by weight of the fibers, a cationic latex fixing agent of 1 to 20% by weight of the styrene-butadiene latex, and water with a solid content concentration of 0.5 to 4% by weight is prepared. A calcium silicate polymer characterized in that when the slurry is poured into a papermaking vat, an anionic polymer flocculant is added dropwise in an amount ranging from 20 to 10,000 pp- of the solid content of the slurry. Pertains to a method of manufacturing a composite plate.
[作 用]
本発明方法は珪酸カルシウム水和物とセルローズ繊維を
含有する水性スラリー中に、該珪酸カルシウム水和物1
00重量部に対しスチレン・ブタジエンラテックスを3
〜15重量部の範囲内で添加し、スチレン・ブタジエン
ラテックスを効率良く定着させるため、カチオン型のラ
テックス定着剤をラテックスに対し0.5〜3重量部添
加して定着後、該スラリーを抄造するものである。[Function] In the method of the present invention, calcium silicate hydrate 1 is added to an aqueous slurry containing calcium silicate hydrate and cellulose fiber.
00 parts by weight of styrene-butadiene latex
In order to efficiently fix the styrene-butadiene latex by adding within the range of ~15 parts by weight, 0.5 to 3 parts by weight of a cationic latex fixing agent is added to the latex, and after fixing, the slurry is made into paper. It is something.
本発明に使用する珪酸カルシウム水和物は珪酸質原料と
石灰原料のCaO/SiO2モル比を0.8〜1.2程
度とし、更に軽量化(嵩が高い)を図るために、使用す
る珪酸質原料の4〜8割を非晶質の珪酸を用い、水蒸気
圧を5kg/c112以上として水熱合成することによ
り得られる。上記の条件下で合成された珪酸カルシウム
水和物は10d/g以上の沈降容積を有する。The calcium silicate hydrate used in the present invention has a CaO/SiO2 molar ratio of silicate raw material and lime raw material of about 0.8 to 1.2, and in order to further reduce the weight (high bulk), the silicate It is obtained by hydrothermal synthesis using amorphous silicic acid for 40 to 80% of the raw material and setting the water vapor pressure to 5 kg/c112 or more. Calcium silicate hydrate synthesized under the above conditions has a sedimentation volume of 10 d/g or more.
なお、本明細書に記載する珪酸カルシウム水和物の沈降
容積は以下のようにして測定した:まず、水熱合成法で
得られた珪酸カルシウム水和物の固形分濃度を測定し、
固形分換算量202を秤量し、10100O!メスシリ
ンダーに移し、蒸留水で1000ml標線までメスアッ
プしたのち、スラリーが漏れないようにメスシリンダー
を上下に10回転倒混合させた後、静1する。24時間
後に固形分が占める容積を読み取り、1請当たりに換算
して沈降容積とする。The sedimentation volume of the calcium silicate hydrate described in this specification was measured as follows: First, the solid content concentration of the calcium silicate hydrate obtained by the hydrothermal synthesis method was measured,
Weighed the solid content equivalent amount 202 and found 10100O! Transfer to a measuring cylinder and make up to 1000 ml with distilled water to the marked line. Mix by inverting the measuring cylinder up and down 10 times to prevent the slurry from leaking, and then let stand. After 24 hours, the volume occupied by the solids is read and converted to the sedimentation volume per contract.
本発明方法においては、上記珪酸カルシウムの水性スラ
リーに予め抄造に適するようにP氷炭 ゛(C3F)3
50s+1以下に叩解したセルローズ繊維を加えること
によって水性スラリーを調製する。In the method of the present invention, P ice charcoal (C3F)3 is added to the aqueous slurry of calcium silicate in advance to make it suitable for papermaking.
An aqueous slurry is prepared by adding cellulose fibers beaten to below 50s+1.
セルローズ繊維としてはNBKP、LBKP等を使用で
きる。セルローズ繊維の添加量は水性スラリーの固形分
の1〜5重量%程度が適当である。NBKP, LBKP, etc. can be used as the cellulose fiber. The appropriate amount of cellulose fiber added is about 1 to 5% by weight of the solid content of the aqueous slurry.
セルローズ繊維の添加量が5重量%を超えると、不燃性
を要求される珪酸カルシウム・ポリマー複合板はその性
能を低下するために好ましくなく、また、1重量%未満
では抄造時の微細粒子の逸失が多くなり、所定配合成分
から欠は離れた成分構成になり、製品の強度などの特性
が低下するために好ましくない。If the amount of cellulose fiber added exceeds 5% by weight, the performance of the calcium silicate/polymer composite plate, which is required to be non-flammable, will deteriorate, making it undesirable.If it is less than 1% by weight, fine particles may be lost during paper making. This is undesirable because it increases the number of ingredients in the product, resulting in a component composition that is far removed from the prescribed ingredients, and properties such as strength of the product deteriorate.
本発明においてはセルローズ繊維を使用することにより
抄造性を向上させ、更に得られた成形板の強度の向上に
も寄与するが、更に必要に応じてガラス繊維、ビニロン
繊維、アクリル繊維等と併用し、得られた成形板の強度
及び耐衝撃性の向上を図ることもできる。In the present invention, the use of cellulose fiber improves paper formability and also contributes to improving the strength of the obtained molded plate, but if necessary, it may also be used in combination with glass fiber, vinylon fiber, acrylic fiber, etc. It is also possible to improve the strength and impact resistance of the obtained molded plate.
本発明方法においては、珪酸カルシウム水和物及びセル
ローズ繊維を含有する水性スラリーに、スチレン・ブタ
ジエンラテックスを添加するのでスラリーのP水性が極
端に低下する。そのため抄造性も一段と悪くなる。抄造
の際、P水性を向上し且つ添加ラテックスの定着率を高
めるためにカチオン型の定着剤を添加することを必須と
する。In the method of the present invention, since styrene-butadiene latex is added to an aqueous slurry containing calcium silicate hydrate and cellulose fiber, the P aqueous property of the slurry is extremely reduced. As a result, the papermaking properties are further deteriorated. During papermaking, it is essential to add a cationic fixing agent in order to improve the P aqueous property and the fixing rate of the added latex.
これらの定着剤の添加量は上記スラリー中に添加したス
チレン・ブタジエンラテックスに対して0.5〜20重
1%が効率良く抄造でき且つスチレン・ブタジエンラテ
ックスが成形板に及ぼす性能を発揮する見地からも必要
である。The amount of these fixing agents added is 0.5 to 20% by weight based on the styrene-butadiene latex added to the slurry, from the viewpoint of efficient paper making and the performance of the styrene-butadiene latex on the molded plate. is also necessary.
上記珪酸カルシウム水和物、セルローズ繊維、スチレン
・ブタジエンラテックス及びカチオン型のラテックス定
着剤を含有する水性スラリーの固形分濃度は0.5〜4
重1%程度に調整して抄造に用いるのが好ましい。The solid content concentration of the aqueous slurry containing the calcium silicate hydrate, cellulose fiber, styrene-butadiene latex, and cationic latex fixative is 0.5 to 4.
It is preferable to adjust the weight to about 1% and use it for papermaking.
上記のようにカチオン型のラテックス定着剤を添加する
ことにより得られたスラリーの抄造性を更に向上させる
ためには、安定なフロックを形成することが必要と思わ
れる。そのためには、まず、カチオン型のラテックス定
着剤を添加し、次に、アニオン型高分子凝集剤を添加す
るのが望ましい。In order to further improve the papermaking properties of the slurry obtained by adding a cationic latex fixing agent as described above, it seems necessary to form stable flocs. For this purpose, it is desirable to first add a cationic latex fixing agent and then add an anionic polymer flocculant.
アニオン型高分子凝集剤の添加量はスラリー中の固形分
に対し20〜10000 ppmの範囲内であり、この
範囲内の添加量で安定なフロックを有するスラリーを得
ることができる。アニオン型高分子凝集剤の具体例とし
てはポリアクリルアミド系のものが挙げられる。The amount of the anionic polymer flocculant added is within the range of 20 to 10,000 ppm based on the solid content in the slurry, and a slurry having stable flocs can be obtained with the amount added within this range. Specific examples of anionic polymer flocculants include polyacrylamide-based ones.
上記アニオン型高分子凝集剤を添加したスラリーは丸網
、長網またはフローオン方式の抄造機によって抄造され
、得られたシート材を乾燥するか、必要に応じてプレス
を施すことにより加圧・成形して嵩比重を高くすること
も可能である。The slurry to which the anionic polymer flocculant has been added is made into paper using a circular wire, Fourdrinier, or flow-on type paper making machine, and the resulting sheet material is dried or, if necessary, pressurized by pressing. It is also possible to increase the bulk specific gravity by molding.
[実 施 例]
以下に実施例を挙げて本発明による珪酸カルシウム・ポ
リマー複合板の製造方法を更に説明する。[Example] The method for manufacturing a calcium silicate/polymer composite plate according to the present invention will be further explained by giving examples below.
珪 カルシウム の 造
下記の第1表に記載する原料配合及び水熱合成条件下で
沈降容積6簡1/g、8d/g、10ml/g、13m
l/g及び16d、’gの珪酸カルシウム水和物[ゾノ
トライト(以下、Xoと略称する)]を得た。Preparation of silica and calcium Under the raw material composition and hydrothermal synthesis conditions listed in Table 1 below, the sedimentation volume is 6 ml/g, 8 d/g, 10 ml/g, and 13 m.
A calcium silicate hydrate [xonotlite (hereinafter abbreviated as Xo)] of l/g and 16d,'g was obtained.
大IL上2癖り
上述のようにして製造された沈降容積10ml/9.1
3mN/g及び16ml/gのXo固形100重量部に
カルボキシ変性スチレン・ブタジェン共重合体ラテック
ス8重量部、P木皮300wblのセルローズ繊維5重
量部(スラリー固形分に対し4.39重量%)、定着剤
としてカヂオン型のポリジアルキルアミノアルキル(メ
タ)クリレート0.8重量部(ラテックスに対し10重
量%)及び水5000重量部を添加・混合してスラリー
濃度2.2重量%のスラリーを調製した。Large IL top 2 sedimentation volume 10ml/9.1 produced as above
100 parts by weight of Xo solids at 3 mN/g and 16 ml/g, 8 parts by weight of carboxy-modified styrene-butadiene copolymer latex, 5 parts by weight of cellulose fibers with P bark of 300 wbl (4.39% by weight based on the solid content of the slurry), and fixed. A slurry having a slurry concentration of 2.2% by weight was prepared by adding and mixing 0.8 parts by weight of cation type polydialkylaminoalkyl (meth)acrylate (10% by weight based on the latex) and 5000 parts by weight of water as an agent.
次に、上述のスラリーに凝集剤としてアニオン性ポリア
ク、リルアミドをO,C134重量部(スラリー中の固
形分に対し300 ppm)を添加して丸網抄造法によ
り抄造し、得られた生板を110″Cで乾燥することに
より厚さ6−輪の珪酸カルシウム・ポリマー複合板を製
造した。得られた複合板の特性を以下の第2表に記載す
る。Next, 134 parts by weight of O and C (300 ppm based on the solid content in the slurry) of anionic polyacrylate and lylamide as a flocculant were added to the above-mentioned slurry, and the resulting green board was made into a paper sheet using a circular paper making method. A 6-ring thick calcium silicate polymer composite board was produced by drying at 110"C. The properties of the resulting composite board are listed in Table 2 below.
大、lL生ニョト
種々の濃度のスラリーを得るために添加水分量を変化さ
せた以外は実施例1と同じ配合を使用して珪酸カルシウ
ム・ポリマー複合板を製造した。Calcium silicate-polymer composite plates were manufactured using the same formulation as in Example 1, except that the amount of water added was varied to obtain slurries of various concentrations.
添加水分量及び得られた複合板の特性を以下の第3表に
記載する。The amount of added water and the properties of the resulting composite board are listed in Table 3 below.
9〜11 ・ 1
沈降容積8me/g、10輸1/9.13論1/g及び
16d/gのXo固形100重量部にカルボキシ変性ス
チレン・ブタジェン共重合体ラテックス8重量部、P氷
炭300afのセルローズ繊維5重量部(スラリー固形
分に対し4.36重量%)、定着剤としてカチオン型の
ポリジアルキルアミノアルキル(メタ)クリレート0.
8重量部(ラテックスに対し10重量%)、ガラス繊維
1重量部及び水5600重量部を添加・混合してスラリ
ー濃度2.0重量%のスラリーを調製した。9-11 ・1 Sedimentation volume 8 me/g, 100 parts by weight of Xo solids of 1/9.13 theory 1/g and 16 d/g, 8 parts by weight of carboxy-modified styrene-butadiene copolymer latex, 300 af of P ice charcoal 5 parts by weight of cellulose fiber (4.36% by weight based on the solid content of the slurry), 0.0 parts by weight of cationic polydialkylaminoalkyl (meth)acrylate as a fixing agent.
8 parts by weight (10% by weight based on latex), 1 part by weight of glass fiber and 5,600 parts by weight of water were added and mixed to prepare a slurry having a slurry concentration of 2.0% by weight.
次に、上述のスラリーに凝集剤としてアニオン性ポリア
クリルアミドを0.034重量部(スラリー中の固形分
に対し300 ppm)を添加して丸網抄造法により抄
造し、得られた生板を110℃で乾燥することにより厚
さ6−−の珪酸カルシウム・ポリマー複合板を製造した
。得られた複合板の特性ル遺11λご」L
沈降容積10閣1/9.13鵬1/g及び16醜1/g
のXO固形100重量部にセルローズ繊維4.5重量部
(スラリー固形分に対し4.26重量%)、ガラス繊維
1重量部及び水5600重量部を添加・混合してスラリ
ー濃度2.0重量%のスラリーを調製した。Next, 0.034 parts by weight of anionic polyacrylamide (300 ppm based on the solid content in the slurry) was added to the above slurry as a coagulant, and the resulting green board was made into paper using a round net paper making method. A calcium silicate/polymer composite plate having a thickness of 6 mm was produced by drying at .degree. Characteristics of the obtained composite plate: 11λ 1/g, sedimentation volume 10 1/9, 13 1/g and 16 1/g
4.5 parts by weight of cellulose fiber (4.26% by weight based on the slurry solid content), 1 part by weight of glass fiber, and 5600 parts by weight of water were added and mixed to 100 parts by weight of XO solid to make a slurry concentration of 2.0% by weight. A slurry was prepared.
次に、上述のスラリーに凝集剤としてアニオン性ポリア
クリルアミドを0.034重量部(スラリー中の固形分
に対し300 ppm)を添加して丸網抄造法により抄
造し、得られた生板を110”Cで乾燥することにより
厚さ6−の成形板を製造した。Next, 0.034 parts by weight of anionic polyacrylamide (300 ppm based on the solid content in the slurry) was added to the above slurry as a coagulant, and the resulting green board was made into paper using a round net paper making method. A molded plate with a thickness of 6 mm was produced by drying at C.
得られた成形板の特性を以下の第5表に記載する。The properties of the molded plate obtained are listed in Table 5 below.
±淑」LΣ
消石灰100重量部、珪藻土44重量部、珪砂51重量
部、パーライト15重量部、セルローズ繊維11重量部
及び水5300重1部を添加・混合して沈降容積6d/
gの混合物スラリーを調製した。 得られた混合物スラ
リーを丸網抄造法にて抄造し、次に従来法によりオート
クレーブ処理して厚さ6+amの珪酸カルシウム板を製
造した。この珪酸カルシウム板の曲げ強度はタテ100
ky/cI112、ヨコ70 kg/ am2と高い
値を示したが、嵩比重も0.82と高い値を示した。±Shuku" LΣ Add and mix 100 parts by weight of slaked lime, 44 parts by weight of diatomaceous earth, 51 parts by weight of silica sand, 15 parts by weight of perlite, 11 parts by weight of cellulose fiber and 1 part by weight of 5,300 parts of water to create a settling volume of 6 d/
A mixture slurry of g was prepared. The resulting mixture slurry was made into a paper using a round net paper making method, and then autoclaved using a conventional method to produce a calcium silicate plate having a thickness of 6+am. The bending strength of this calcium silicate plate is 100
It showed a high value of ky/cI of 112 and width of 70 kg/am2, but its bulk specific gravity also showed a high value of 0.82.
雌1」忙
消石灰100重量部、珪藻±44重1部、珪砂51重量
部、パーライト60重量部、セルローズ繊維13重量部
及び水8500重量部を添加・混合して沈降容積8ml
/Hの混合物スラリーを調製した。 得られた混合物ス
ラーリーを使用して比較例6と同様の操作により厚さ6
−の珪酸カルシウム板を製造した。この珪酸カルシウム
板の曲げ強度はタテ43 ky/ cm’、ヨコ28
ky/ cm2であり、嵩比重は0.61であった。Add and mix 100 parts by weight of slaked lime, 1 part by weight of diatom ±44 parts, 51 parts by weight of silica sand, 60 parts by weight of perlite, 13 parts by weight of cellulose fiber and 8500 parts by weight of water to obtain a sedimentation volume of 8 ml.
/H mixture slurry was prepared. Using the obtained mixture slurry, the same operation as in Comparative Example 6 was performed to obtain a thickness of 6.
A calcium silicate plate of - was manufactured. The bending strength of this calcium silicate plate is 43 ky/cm' vertically and 28 ky/cm' horizontally.
ky/cm2, and the bulk specific gravity was 0.61.
12〜18. γ
種々の濃度のスラリーを得るために添カロ水分量を変化
させた以外は実施例1と同じ配合を使用して珪酸カルシ
ウム・ポリマー複合板を製造した。12-18. γ Calcium silicate/polymer composite plates were manufactured using the same formulation as in Example 1, except that the amount of added caloric water was varied to obtain slurries of various concentrations.
添加水分量及び得られた複合板の特性を以下の第6表に
記載する。The amount of added water and the properties of the resulting composite board are listed in Table 6 below.
方 19〜20 ・ 8〜10ス
ラリ一濃度2.3重量%及び2.1重量%の実施例9と
同じ配合のスラリーを製造し、実施例9と同様の方法で
丸網抄造法にて珪酸カルシウム・ポリマー複合板を製造
した。Methods 19-20 - 8-10 Slurries were prepared with the same composition as in Example 9 with a concentration of 2.3% by weight and 2.1% by weight, and silicic acid was added using the same method as in Example 9 using the circular paper making method. A calcium-polymer composite board was manufactured.
また、比較品として以下に記載する配合をもつスラリー
を使用してモールドプレス法にて成形板を製造した。In addition, as a comparison product, a molded plate was manufactured by a mold press method using a slurry having the formulation described below.
比較品を製造する時に使用するスラリーは沈降容積10
−1/gのXo固形100重量部にカルボキシ変性スチ
レン・ブタジェン共重合体ラテックス8重量部、セルロ
ーズ繊維1.5重量部(スラリー固形分に対し1.29
重量%)、定着剤としてカチオン型のポリジアルキルア
ミノアルキル(メタ)クリレート0.8重量部(ラテッ
クスに対し10重量%)、ガラス繊維6重量部よりなる
。なお、スラリー濃度は第7表に記載する。The slurry used to produce the comparative product had a sedimentation volume of 10
-1/g of Xo solids, 8 parts by weight of carboxy-modified styrene-butadiene copolymer latex, 1.5 parts by weight of cellulose fiber (1.29 parts by weight based on the solid content of the slurry)
% by weight), 0.8 parts by weight of cationic polydialkylaminoalkyl (meth)acrylate as a fixing agent (10% by weight based on the latex), and 6 parts by weight of glass fiber. Note that the slurry concentration is listed in Table 7.
!」ゴI上二二と
実施例9及び10で丸網抄造法で得た生板をプレスして
嵩比重を調整して厚さ6輪部の珪酸カルシウム・ポリマ
ー複合板を製造した。得られた珪酸カルシウム・ポリマ
ー複合板の特性を以下の第8表に記載する。! A calcium silicate/polymer composite board having a thickness of 6 rings was produced by pressing the raw boards obtained by the round net papermaking method in Examples 9 and 10 to adjust the bulk specific gravity. The properties of the obtained calcium silicate/polymer composite board are listed in Table 8 below.
[発明の効果]
本発明は予め水熱合成により得られた特定の沈降容積を
有する珪酸カルシウム水和物を使用し、更に、抄造の際
のスラリー濃度を規定することにより抄造法による珪酸
カルシウム板の従来の製造法を改良したものであり、軽
量、高強度、更に靭性に富む切削加工性を高めた薄物珪
酸カルシウム・ポリマー複合板を効率良く製造し得るも
のである。[Effects of the Invention] The present invention uses calcium silicate hydrate having a specific sedimentation volume obtained in advance by hydrothermal synthesis, and further specifies the slurry concentration during papermaking, thereby producing a calcium silicate board by a papermaking method. This method is an improvement on the conventional manufacturing method, and enables the efficient production of thin calcium silicate/polymer composite plates that are lightweight, have high strength, are tough, and have improved machinability.
Claims (1)
物100重量部、スチレン・ブタジエンラテックス3〜
15重量部、ろ水度が350ml以下のセルローズ繊維
をスラリー固形分の1〜5重量%、カチオン型のラテッ
クス定着剤を前記スチレンブタジエンラテックス重量の
1〜20重量%及び水を調合して固形分濃度0.5〜4
重量%のスラリーを得、該スラリーを抄造バットに注入
する際に、更にアニオン型高分子凝集剤をスラリーの固
形分の20〜10000ppmの範囲の量で滴下して抄
造することを特徴とする珪酸カルシウム・ポリマー複合
板の製造方法。 2、スラリーが無機繊維及び有機繊維からなる群から選
択された1種または2種以上の繊維を含有する特許請求
の範囲第1項記載の珪酸カルシウム・ポリマー複合板の
製造方法。[Claims] 1. 100 parts by weight of calcium silicate hydrate having a sedimentation volume of 10 ml/g or more, styrene-butadiene latex 3-
15 parts by weight, cellulose fibers with a freeness of 350 ml or less are mixed into a slurry with a solid content of 1 to 5% by weight, a cationic latex fixing agent is mixed with 1 to 20% by weight of the styrene-butadiene latex, and water to make a solid content. Concentration 0.5-4
% by weight, and when the slurry is injected into a papermaking vat, an anionic polymer flocculant is further added dropwise in an amount ranging from 20 to 10,000 ppm of the solid content of the slurry. Method for manufacturing calcium-polymer composite board. 2. The method for producing a calcium silicate/polymer composite board according to claim 1, wherein the slurry contains one or more types of fibers selected from the group consisting of inorganic fibers and organic fibers.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4969088A JPH0818857B2 (en) | 1988-03-04 | 1988-03-04 | Method for producing calcium silicate-polymer composite plate |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4969088A JPH0818857B2 (en) | 1988-03-04 | 1988-03-04 | Method for producing calcium silicate-polymer composite plate |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01224253A true JPH01224253A (en) | 1989-09-07 |
JPH0818857B2 JPH0818857B2 (en) | 1996-02-28 |
Family
ID=12838180
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4969088A Expired - Fee Related JPH0818857B2 (en) | 1988-03-04 | 1988-03-04 | Method for producing calcium silicate-polymer composite plate |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0818857B2 (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6525116B2 (en) | 1999-01-26 | 2003-02-25 | National Gypsum Properties Llc | Gypsum composition with ionic styrene butadiene latex additive |
JP2006143534A (en) * | 2004-11-19 | 2006-06-08 | Taiheiyo Cement Corp | Calcium silicate hardened body and its production method |
WO2013178417A1 (en) * | 2012-05-29 | 2013-12-05 | Construction Research & Technology Gmbh | Pulverulent accelerator |
US9926233B2 (en) | 2014-12-18 | 2018-03-27 | Basf Se | Construction chemical composition for tile mortar |
CN110330305A (en) * | 2019-07-15 | 2019-10-15 | 重庆大学 | A kind of hydrated calcium silicate imitated wood material and preparation method thereof |
CN114805640A (en) * | 2022-04-20 | 2022-07-29 | 青岛科技大学 | Non-acid flocculation method of styrene-butadiene latex |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3624434B1 (en) | 2017-07-07 | 2021-06-02 | Huawei Technologies Co., Ltd. | Terminal provided with camera, and photographing method |
-
1988
- 1988-03-04 JP JP4969088A patent/JPH0818857B2/en not_active Expired - Fee Related
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6525116B2 (en) | 1999-01-26 | 2003-02-25 | National Gypsum Properties Llc | Gypsum composition with ionic styrene butadiene latex additive |
JP2006143534A (en) * | 2004-11-19 | 2006-06-08 | Taiheiyo Cement Corp | Calcium silicate hardened body and its production method |
WO2013178417A1 (en) * | 2012-05-29 | 2013-12-05 | Construction Research & Technology Gmbh | Pulverulent accelerator |
US9926233B2 (en) | 2014-12-18 | 2018-03-27 | Basf Se | Construction chemical composition for tile mortar |
CN110330305A (en) * | 2019-07-15 | 2019-10-15 | 重庆大学 | A kind of hydrated calcium silicate imitated wood material and preparation method thereof |
CN114805640A (en) * | 2022-04-20 | 2022-07-29 | 青岛科技大学 | Non-acid flocculation method of styrene-butadiene latex |
CN114805640B (en) * | 2022-04-20 | 2023-06-20 | 青岛科技大学 | Non-acid flocculation method for styrene-butadiene latex |
Also Published As
Publication number | Publication date |
---|---|
JPH0818857B2 (en) | 1996-02-28 |
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