JP2665942B2 - Calcium silicate hydrate compact and method for producing the same - Google Patents

Calcium silicate hydrate compact and method for producing the same

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Publication number
JP2665942B2
JP2665942B2 JP63162242A JP16224288A JP2665942B2 JP 2665942 B2 JP2665942 B2 JP 2665942B2 JP 63162242 A JP63162242 A JP 63162242A JP 16224288 A JP16224288 A JP 16224288A JP 2665942 B2 JP2665942 B2 JP 2665942B2
Authority
JP
Japan
Prior art keywords
calcium silicate
fiber
raw material
silicate hydrate
potassium titanate
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 - Fee Related
Application number
JP63162242A
Other languages
Japanese (ja)
Other versions
JPH029740A (en
Inventor
紀八郎 西内
正志 吉崎
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Otsuka Chemical Co Ltd
Original Assignee
Otsuka Chemical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Otsuka Chemical Co Ltd filed Critical Otsuka Chemical Co Ltd
Priority to JP63162242A priority Critical patent/JP2665942B2/en
Publication of JPH029740A publication Critical patent/JPH029740A/en
Application granted granted Critical
Publication of JP2665942B2 publication Critical patent/JP2665942B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は珪酸カルシウム水和物成形体及びその製造方
法に関する。
The present invention relates to a calcium silicate hydrate compact and a method for producing the same.

(従来の技術) 近年、珪酸カルシウム水和物成形体が多く製造されて
いる。これらの珪酸カルシウム化合物は耐候性、耐火性
に優れており、工業材料としてはプラスチツク用充填
剤、触媒、吸着剤などに使用されるばかりでなく、内外
装材、断熱材、吸音材、耐火被覆材、軽量気泡コンクリ
ート(ALC)などの建材用に数多く用いられている。
(Prior art) In recent years, a large number of calcium silicate hydrate compacts have been manufactured. These calcium silicate compounds have excellent weather resistance and fire resistance, and are used not only as fillers for plastics, catalysts, adsorbents, etc. as industrial materials, but also as interior and exterior materials, heat insulating materials, sound absorbing materials, and fire-resistant coatings. It is widely used for building materials such as wood and lightweight cellular concrete (ALC).

珪酸カルシウム水和物系の工業材料や内外装材、断熱
材、吸音材、耐火被覆材、ALCなどの建材の製造方法は
いずれもオートクレーブ中で珪酸質原料と石灰質原料と
を反応させて珪酸カルシウム結晶を生成させた後にこの
スラリーを加圧成形して乾燥硬化する方法か、又は予め
加熱し、ゲル化した状態で加圧成形し、オートクレーブ
養生後に乾燥させる方法が用いられている。しかしなが
らこれらの珪酸カルシウム水和物を生成させ、成形体を
得るには長時間の加熱、加圧が必要であり、工程の短縮
化が必要であつた。又このようにして得られた成形体は
建材などに用いられるため高強度である必要があるが、
強度の点についても性能の向上が求められている。
In the manufacturing methods of calcium silicate hydrate-based industrial materials, interior and exterior materials, heat insulation materials, sound absorbing materials, fireproof coating materials, and ALC, all of the production methods for calcium silicate are performed by reacting siliceous raw materials and calcareous raw materials in an autoclave. Either a method in which the slurry is pressure-formed and dried and hardened after the formation of crystals, or a method in which the slurry is pre-heated, pressure-formed in a gelled state, and dried after autoclaving. However, in order to produce these calcium silicate hydrates and obtain a molded body, it is necessary to apply heat and pressure for a long time, and it is necessary to shorten the process. Also, since the molded body obtained in this way is used for building materials, etc., it is necessary to have high strength,
There is also a demand for improved performance in terms of strength.

(発明が解決しようとする課題) 本発明の目的は短い反応時間で優れた強度を有する珪
酸カルシウム水和物成形体を製造する方法及び得られた
珪酸カルシウム水和物成形体を提供することにある。
(Problems to be Solved by the Invention) An object of the present invention is to provide a method for producing a calcium silicate hydrate compact having excellent strength in a short reaction time, and to provide the obtained calcium silicate hydrate compact. is there.

(課題を解決するための手段) 本発明は石灰質原料と珪酸質原料と水を高温高圧飽和
水蒸気下で水熱反応させるに際し、石灰室原料と珪酸質
原料とをCaO、SiO2に換算してモル比で前者に対して後
者を0.8〜1.2の割合で配合し、チタン酸カリウムを添加
して成形した後、反応温度180〜220℃で水熱反応させる
ことを特徴とする主としてゾノトライトからなる珪酸カ
ルシウム水和物成形体の製造方法及びチタン酸カリウム
を含有し、主としてゾノトライトからなる珪酸カルシウ
ム水和物成形体に係る。
(Means for Solving the Problems) In the present invention, when a calcareous raw material, a siliceous raw material and water are subjected to a hydrothermal reaction under high-temperature and high-pressure saturated steam, the calcareous raw material and the siliceous raw material are converted into CaO and SiO 2. Silicic acid mainly composed of zonotrite, characterized in that the former is blended at a molar ratio of 0.8 to 1.2 with respect to the former, and potassium titanate is added and molded, followed by a hydrothermal reaction at a reaction temperature of 180 to 220 ° C. The present invention relates to a method for producing a calcium hydrate molded product and a calcium silicate hydrate molded product containing potassium titanate and mainly composed of zonotrite.

本発明において用いられるチタン酸カリウムは一般に K2O・nTiO2・mH2O (n及びmはそれぞれ1<n≦8、0≦m≦4の実数を
示す)で表わされる。チタン酸カリウムの添加量は通
常、珪酸質原料と石灰質原料の合計に対して約3〜40%
(重量%)、好ましくは約5〜30%とするのがよい。
The potassium titanate used in the present invention is generally represented by K 2 O.nTiO 2 .mH 2 O (n and m are real numbers of 1 <n ≦ 8 and 0 ≦ m ≦ 4, respectively). The amount of potassium titanate is usually about 3 to 40% of the total of siliceous raw material and calcareous raw material.
(% By weight), preferably about 5 to 30%.

本発明に用いられる珪酸質原料としては従来の水熱反
応に用いられる原料であればよく、例えば珪石、珪藻
土、シラス、白土、珪砂、フライアツシユ、シリカフラ
ワー、ゼオライトなどがある。石灰質原料としては消石
灰、生石灰、ポルトランドセメント、スラグなどを使用
することができる。これら珪酸質原料と石灰質原料との
使用割合はCaO、SiO2に換算してモル比で前者に対して
後者を0.8〜1.2にするのが好ましい。これらの原料は通
常水性スラリーの状態に調製される。このスラリー濃度
は約3〜10%程度が適当である。調製されたスラリーは
オートクレーブ中で加熱反応させる。加熱反応は通常2
段階で行われる。第1段階は90〜100℃、30分〜2時間
ぐらい加熱することによつてゲル化状態をつくり、次い
でプレス型に充填して加圧脱水して成型する。成型物を
オートクレーブ中で180〜220℃の加熱反応を行い珪酸カ
ルシウム水和物成形体を得る。しかし一段階加熱で行う
場合もある。
The siliceous raw material used in the present invention may be any raw material used in a conventional hydrothermal reaction, and examples thereof include silica stone, diatomaceous earth, shirasu, clay, silica sand, fly ash, silica flower, and zeolite. Slaked lime, quicklime, Portland cement, slag, and the like can be used as the calcareous raw material. The ratio of these siliceous material and calcareous material are CaO, preferably the latter to 0.8 to 1.2 with respect to the former in a molar ratio in terms of SiO 2. These raw materials are usually prepared in the form of an aqueous slurry. The appropriate slurry concentration is about 3 to 10%. The prepared slurry is heated and reacted in an autoclave. Heating reaction is usually 2
Done in stages. In the first step, a gelled state is created by heating at 90 to 100 ° C. for about 30 minutes to 2 hours, and then filled into a press mold and dewatered under pressure to mold. The molded product is subjected to a heating reaction at 180 to 220 ° C. in an autoclave to obtain a calcium silicate hydrate molded product. However, it may be performed by one-stage heating.

本発明で生成される珪酸カルシウム水和物は主として
ゾノトライトの結晶構造を持つたものである。
The calcium silicate hydrate produced in the present invention has mainly the crystal structure of zonotolite.

本発明ではこれらの原料の他に繊維補強材を併用する
ことも可能である。この場合、繊維補強材としては耐ア
ルカリ性ガラス繊維、ロツクウール繊維、炭素繊維、合
成繊維、パルプ、金属繊維、有機繊維などやウイスカー
類が挙げられる。これら補強材は石灰質原料や珪酸質原
料等に配合して使用され、その配合量は通常、石灰質原
料と珪酸質原料の合計に対して約1〜30%とするのが良
い。
In the present invention, it is possible to use a fiber reinforcing material in addition to these raw materials. In this case, examples of the fiber reinforcing material include alkali-resistant glass fiber, rock wool fiber, carbon fiber, synthetic fiber, pulp, metal fiber, organic fiber, and whiskers. These reinforcing materials are used in a mixture with a calcareous raw material, a siliceous raw material, and the like, and the compounding amount is usually preferably about 1 to 30% based on the total of the calcareous raw material and the siliceous raw material.

(実 施 例) 以下に実施例により更に詳しく説明する。単に部とあ
るは重量部を示す。
(Example) Hereinafter, an example will be described in more detail. “Parts” simply means “parts by weight”.

実施例1 消石灰(樫野石灰)、珪石(東海工業)を用いそれぞ
れ粉砕し、180メツシユ全通した粉体をCaO/SiO2のモル
比で1.0に調整し、上記調整した原料100部に対してチタ
ン酸カリウムウイスカー(大塚化学、商品名テイスモ
D)5部及び水1500部を加えて撹拌し、均一なスラリー
とした。このスラリーをオートクレーブ中で95〜100℃
で2時間加熱してゲル化させた後プレス型に充填し、加
圧脱水して成型した。この成型物をオートクレーブ中で
6時間、200℃で反応させた後、取り出して110℃で一夜
乾燥した。この成型体のかさ比重は0.37であつた。
Example 1 Using slaked lime (Kashino lime) and silica stone (Tokai Kogyo), each was pulverized, and the powder passed through 180 mesh was adjusted to 1.0 with a molar ratio of CaO / SiO 2 to 100 parts of the adjusted raw material. 5 parts of potassium titanate whiskers (Otsuka Chemical Co., trade name: Teismo D) and 1500 parts of water were added and stirred to obtain a uniform slurry. This slurry is placed in an autoclave at 95 to 100 ° C.
After heating for 2 hours to form a gel, the mixture was filled into a press mold, dewatered under pressure and molded. The molded product was reacted at 200 ° C. for 6 hours in an autoclave, taken out and dried at 110 ° C. overnight. The bulk specific gravity of this molded product was 0.37.

実施例2〜4 チタン酸カリウムウイスカーをそれぞれ10部、20部、
30部添加した他は実施例1と同様にして成形体を得た。
Examples 2 to 4 10 parts each of potassium titanate whiskers, 20 parts,
A molded product was obtained in the same manner as in Example 1 except that 30 parts were added.

実施例5 オートクレーブ中、200℃での反応時間を3時間とし
た他は実施例1と同様にして成形体を得た。
Example 5 A molded article was obtained in the same manner as in Example 1 except that the reaction time at 200 ° C. in the autoclave was changed to 3 hours.

比較例1 チタン酸カリウムウイスカーを添加せず、水の添加量
を300部にした他は実施例1と同様にして成形体を得
た。
Comparative Example 1 A molded body was obtained in the same manner as in Example 1, except that the potassium titanate whisker was not added and the amount of water was changed to 300 parts.

比較例2 オートクレーブ中、200℃での反応時間を12時間とし
た他は比較例1と同様にして成形体を得た。
Comparative Example 2 A molded article was obtained in the same manner as in Comparative Example 1, except that the reaction time at 200 ° C. in an autoclave was changed to 12 hours.

実施例1〜5及び比較例1〜2で得られた成形体の曲
げ強度(JIS A 1408で測定)を第1表に示す。
Table 1 shows the bending strength (measured by JIS A 1408) of the molded articles obtained in Examples 1 to 5 and Comparative Examples 1 and 2.

(発明の効果) 本発明においては珪酸カルシルム水和物成形体を製造
するに際し、チタン酸カリウムを添加することによつ
て、短い反応時間により高強度の成形体の取得が可能で
ある。
(Effect of the Invention) In the present invention, when a calcium silicate hydrate molded article is produced, by adding potassium titanate, a high-strength molded article can be obtained in a short reaction time.

Claims (3)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】チタン酸カリウムを含有し、主としてゾノ
トライトからなる珪酸カルシウム水和物成形体。
1. A calcium silicate hydrate compact comprising potassium titanate and mainly consisting of zonotrite.
【請求項2】更に繊維補強材として耐アルカリ性ガラス
繊維、ロツクウール繊維、炭素繊維、合成繊維、パル
プ、金属繊維、有機繊維又はウイスカーの1種又は2種
以上を配合した請求項1記載の珪酸カルシウム水和物成
形体。
2. The calcium silicate according to claim 1, further comprising one or more of alkali-resistant glass fiber, rock wool fiber, carbon fiber, synthetic fiber, pulp, metal fiber, organic fiber and whisker as a fiber reinforcing material. Hydrate molded body.
【請求項3】石灰質原料と珪酸質原料と水を高温高圧飽
和水蒸気下で水熱反応させるに際し、石灰室原料と珪酸
質原料とをCaO、SiO2に換算してモル比で前者に対して
後者を0.8〜1.2の割合で配合し、チタン酸カリウムを添
加して成形した後、反応温度180〜220℃で水熱反応させ
ることを特徴とする主としてゾノトライトからなる珪酸
カルシウム水和物成形体の製造方法。
3. A hydrothermal reaction of a calcareous raw material, a siliceous raw material, and water under a high-temperature, high-pressure saturated steam, wherein the lime-chamber raw material and the siliceous raw material are converted into CaO and SiO 2 in a molar ratio to the former. The latter is blended at a ratio of 0.8 to 1.2, and after adding potassium titanate and molding, a calcium silicate hydrate molded body mainly composed of zonotlite characterized by being subjected to a hydrothermal reaction at a reaction temperature of 180 to 220 ° C. Production method.
JP63162242A 1988-06-28 1988-06-28 Calcium silicate hydrate compact and method for producing the same Expired - Fee Related JP2665942B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63162242A JP2665942B2 (en) 1988-06-28 1988-06-28 Calcium silicate hydrate compact and method for producing the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63162242A JP2665942B2 (en) 1988-06-28 1988-06-28 Calcium silicate hydrate compact and method for producing the same

Publications (2)

Publication Number Publication Date
JPH029740A JPH029740A (en) 1990-01-12
JP2665942B2 true JP2665942B2 (en) 1997-10-22

Family

ID=15750689

Family Applications (1)

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Country Link
JP (1) JP2665942B2 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6654996B1 (en) * 1996-07-17 2003-12-02 Richard T. Harris Tube remover and method for axially removing a metal tube
JP4743379B2 (en) * 2004-08-04 2011-08-10 株式会社風船工房匠 Clean room
JP4920197B2 (en) * 2005-04-05 2012-04-18 高砂熱学工業株式会社 Clean booth

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5838379B2 (en) * 1981-09-09 1983-08-23 財団法人生産開発科学研究所 waterproof cement composition
JPS63107848A (en) * 1986-10-23 1988-05-12 九州耐火煉瓦株式会社 Inorganic fiber reinforced cement composite material

Also Published As

Publication number Publication date
JPH029740A (en) 1990-01-12

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