JPH07126083A - Production of formed inorganic article - Google Patents
Production of formed inorganic articleInfo
- Publication number
- JPH07126083A JPH07126083A JP5270538A JP27053893A JPH07126083A JP H07126083 A JPH07126083 A JP H07126083A JP 5270538 A JP5270538 A JP 5270538A JP 27053893 A JP27053893 A JP 27053893A JP H07126083 A JPH07126083 A JP H07126083A
- Authority
- JP
- Japan
- Prior art keywords
- parts
- starch
- curing
- powder
- weight
- 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
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
- C04B28/00—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
- C04B28/02—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing hydraulic cements other than calcium sulfates
-
- 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
- C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
- C04B2111/30—Nailable or sawable materials
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Organic Chemistry (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は建材、土木用材料として
の無機質成形物の製造方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing an inorganic molded article as a building material or a civil engineering material.
【0002】[0002]
【従来の技術】従来より耐火性、断熱性および強度に優
れた建材および土木用資材として、珪酸カルシウム板や
セメント系無機質板は広く使用されていたが、近年、常
温養生や常圧養生ばかりでなく、短時間に高い強度と優
れた耐久性を有するセメント成型物を製造する方法とし
て高温高圧での蒸気養生、すなわちオートクレーブ養生
が広く用いられるようになった。これらの無機質成形物
の大きな用途として、抄造法による多層突き板や押し出
し成形方法による建物の壁材を中心とした軽量板があ
る。これらは比重が軽くしかも強く強靭な性能が望まれ
ているばかりでなく、釘打ち性や耐凍害性などの厳しい
性能をも要求されている。これらの対策として石綿がセ
メント成形体の流動性や保形性および強度アップの助剤
として必須成分であったが、石綿繊維は人体に有毒であ
ることから、石綿繊維を含有しなくても上記の優れた性
能を有し、オートクレーブ養生可能な組成物の開発が強
く望まれている。石綿の代わりにパルプ、ガラス繊維、
ビニロン繊維やポリプロピレン繊維などが補強材として
添加されかなりの強度の向上につながっいいるが、高い
養生温度に耐えることができなかったり、機械物性や耐
久性が不足する場合が多いという問題が残っている。そ
の他、補強繊維の他にもセメントマトリックスの強度を
向上させ成形物の性能を高める試みが種々なされている
が(たとえば特公昭59−30664号、特開昭64−
56346号)、実際にはシリカヒュームのような超微
粉のシリカを必要とし、量およびコストの面で不利とな
る面が多いのが現状である。2. Description of the Related Art Conventionally, calcium silicate boards and cement-based inorganic boards have been widely used as building materials and civil engineering materials excellent in fire resistance, heat insulation and strength, but in recent years, only room temperature curing and atmospheric curing have been possible. However, steam curing at high temperature and high pressure, that is, autoclave curing has come to be widely used as a method for producing a cement molded product having high strength and excellent durability in a short time. Large applications of these inorganic molded products include a multi-layered veneer made by a papermaking method and a lightweight plate mainly made of a building wall material by an extrusion molding method. Not only are these materials required to have a low specific gravity and are strong and tough, but they are also required to have severe performance such as nailing resistance and frost damage resistance. As these measures, asbestos was an essential component as a fluidity, shape-retaining and strength-enhancing aid for cement compacts, but asbestos fibers are toxic to the human body, so asbestos without asbestos fibers There is a strong demand for the development of a composition capable of curing an autoclave, which has excellent performance as described above. Instead of asbestos, pulp, glass fiber,
Vinylon fiber and polypropylene fiber are added as a reinforcing material, which has led to a considerable improvement in strength, but problems such as being unable to withstand high curing temperatures and often lacking mechanical properties and durability remain. There is. In addition to the reinforcing fibers, various attempts have been made to improve the strength of the cement matrix to enhance the performance of the molded product (for example, Japanese Patent Publication No. 59-30664 and Japanese Patent Laid-Open No. 64-64).
No. 56346), actually, ultrafine silica such as silica fume is required, and there are many disadvantages in terms of quantity and cost under the present circumstances.
【0003】[0003]
【発明が解決しようとする課題】本発明はオートクレー
ブ養生で、高い強度を発現し、さらに折り曲げ性能や釘
打ち性能などの優れた性能を有する無機質成形物の製造
方法を提供するものである。SUMMARY OF THE INVENTION The present invention provides a method for producing an inorganic molded article which is autoclave-cured, exhibits high strength, and has excellent properties such as bending performance and nailing performance.
【0004】[0004]
【課題を解決するための手段】本発明者等は上記の問題
点を解決すべく鋭意検討した結果、石灰質粉末、シリカ
質粉末および補強繊維からなる水硬性配合組成物100
重量部に対して、デンプン系化合物、多価アルコール化
合物および有機酸塩からなる群から選ばれた1種または
2種以上の添加物を0.1〜10重量部添加し、均一混
合、賦形した後、120〜200℃でオートクレーブ養
生することを特徴とする無機質成形物の製造方法を見出
し、本発明に至ったものである。Means for Solving the Problems As a result of intensive studies made by the present inventors in order to solve the above problems, a hydraulic compound composition 100 comprising a calcareous powder, a siliceous powder and a reinforcing fiber is obtained.
0.1 to 10 parts by weight of one or two or more kinds of additives selected from the group consisting of starch compounds, polyhydric alcohol compounds and organic acid salts are added to parts by weight, and uniform mixing and shaping are performed. After that, the present invention has been completed by finding a method for producing an inorganic molded article, which is characterized by performing autoclave curing at 120 to 200 ° C.
【0005】本発明に於ける石灰質粉末としては、通常
のポルトランドセメント、生石灰、消石灰などの一種以
上が用いられる。シリカ質粉末としては、セメント分野
においてポゾランと称されている石灰と水の存在下で徐
々に水硬性を発揮するもので、珪石粉、フライアッシ
ュ、高炉スラグ粉末、シリカヒューム、珪藻土等のシリ
カ分の含有率の高い無機粉体などの1種以上が用いられ
る。補強繊維としては、ガラス繊維、炭素繊維、パルプ
繊維、ビニロン、ポリプロ等の合成繊維などの一種以上
が用いられる。本発明において、さらに骨材、細骨材を
併用するのが好ましく、その一例としては、砂や砕石の
他にパーライトなどの中空骨材が挙げられる。As the calcareous powder used in the present invention, one or more kinds of ordinary Portland cement, quick lime, slaked lime, etc. are used. The siliceous powder is one that gradually exhibits hydraulic properties in the presence of lime and water, which is called pozzolan in the cement field, and has silica content such as silica stone powder, fly ash, blast furnace slag powder, silica fume, and diatomaceous earth. One or more kinds of inorganic powders having a high content of are used. As the reinforcing fiber, one or more kinds of glass fiber, carbon fiber, pulp fiber, synthetic fiber such as vinylon, polypropylene, etc. are used. In the present invention, it is preferable to use an aggregate and a fine aggregate together, and one example thereof is a hollow aggregate such as pearlite in addition to sand and crushed stone.
【0006】石灰質、シリカ質粉末、補強繊維および骨
材の配合割合については特に制限はないが、石灰質10
0重量部に対してシリカ質粉末30〜200重量部、補
強繊維2〜30重量部および骨材4〜70重量部が好ま
しい。There is no particular limitation on the mixing ratio of the calcareous, siliceous powder, reinforcing fiber and aggregate, but calcareous 10
30 to 200 parts by weight of siliceous powder, 2 to 30 parts by weight of reinforcing fibers, and 4 to 70 parts by weight of aggregate are preferable to 0 parts by weight.
【0007】上記の水硬性配合組成物に添加される添加
物としては、デンプン系化合物、多価アルコール化合物
および有機酸塩が挙げられる。デンプン系化合物として
は、トウモロコシデンプン、ジャガイモデンプン、コム
ギデンプン、コメデンプン、タピオカデンプン等の生澱
粉およびこれらの生澱粉を原料にした酸化デンプン、燐
酸エステル化デンプン等の変性デンプンやデキストリン
を指す。これらのデンプン系化合物の中でも生デンプン
が好ましく、さらにトウモロコシデンプンが好ましい。
これらのデンプン系化合物は1種または2種以上を混合
して用いても良い。[0007] Examples of the additives added to the above hydraulic compound composition include starch compounds, polyhydric alcohol compounds and organic acid salts. Examples of the starch-based compound include raw starch such as corn starch, potato starch, wheat starch, rice starch and tapioca starch, and modified starch such as oxidized starch and phosphate esterified starch obtained from these raw starches and dextrin. Of these starch-based compounds, raw starch is preferable, and corn starch is more preferable.
These starch-based compounds may be used alone or in combination of two or more.
【0008】多価アルコール化合物としては、グルコー
ス、しょ糖、ソルビトール、マンニトール、ペンタエリ
スリトール、グリセリン、デキストリンなどが挙げら
れ、特にグルコース、しょ糖、ソルビトールが好まし
く、この中でもソルビトールが好ましい。Examples of the polyhydric alcohol compound include glucose, sucrose, sorbitol, mannitol, pentaerythritol, glycerin and dextrin, and glucose, sucrose and sorbitol are particularly preferable, and sorbitol is particularly preferable.
【0009】有機酸塩としては、グルコン酸塩、ポリア
クリル酸塩、リグニンスルホン酸塩などが挙げられ、こ
の中でもリグニンスルホン酸塩が好ましい。これら有機
酸の塩の種類としては特に限定はなく、ナトリウム塩、
カルシウム塩、マグネシウム塩があり、一般的にはナト
リウム塩である。Examples of the organic acid salt include gluconate, polyacrylic acid, lignin sulfonate and the like, and among these, lignin sulfonate is preferable. There is no particular limitation on the type of salt of these organic acids, sodium salt,
There are calcium salt and magnesium salt, and generally sodium salt.
【0010】本発明のこれらの添加物の添加は、水硬性
配合組成物100重量部に対して、0.1〜10重量部
である。0.1重量部より少ないと添加の効果が得られ
ず、10重量部より多くしても期待した効果が出ないば
かりでなく、やや硬化不良を起こすので好ましくない。The addition amount of these additives of the present invention is 0.1 to 10 parts by weight based on 100 parts by weight of the hydraulic compounding composition. If the amount is less than 0.1 parts by weight, the effect of addition cannot be obtained, and if the amount is more than 10 parts by weight, not only the expected effect is not obtained, but also a curing failure is caused, which is not preferable.
【0011】水硬性配合組成物中に上記添加物を添加す
る方法としては粉体、または液体をそのまま水硬性配合
組成物中に添加した後、加水しても良く、または添加水
の全量または一部に上記添加物を溶解して添加しても良
い。しかし、抄造法などのように大量の水を使用する場
合には、最終配合物中に上記添加量が存在するように濃
度調節を行う必要がある。また上記添加物またはその水
溶液を養生前の成形物に散布したり、養生前の成形物を
上記添加物の水溶液に含浸しても良い。As a method for adding the above-mentioned additive to the hydraulic compounding composition, powder or liquid may be added as it is to the hydraulic compounding composition and then water may be added, or the whole amount or a total amount of the added water may be added. You may melt | dissolve and add the said additive to a part. However, when a large amount of water is used as in the papermaking method, it is necessary to adjust the concentration so that the above-mentioned addition amount is present in the final blend. Further, the above-mentioned additive or its aqueous solution may be sprayed on the molded product before curing, or the molded product before curing may be impregnated with the aqueous solution of the above-mentioned additive.
【0012】本発明におけるオートクレーブ養生は、1
20〜200℃で行われる。オートクレーブ養生の時間
としては3〜24時間が好ましい。尚、オートクレーブ
養生に先だって、5〜80℃で12〜30時間の一次養
生を行うことが好ましく、一次養生は常圧の飽和蒸気圧
下でのスチーム養生がより好ましい。また本発明には上
記添加物以外の添加物を本発明の効果を損なわない範囲
で併用しても差し支えない。その一例としては、メチル
セルロース、ポリビニルアルコールなどの流動性改良
剤、硼酸、硼砂、硼酸カルシウム、硼酸エステルなどの
硼酸系化合物、ステアリン酸カルシウムなどの撥水剤、
泡連行剤などが挙げられる。The autoclave curing in the present invention is 1
It is carried out at 20 to 200 ° C. The autoclave curing time is preferably 3 to 24 hours. In addition, prior to autoclave curing, it is preferable to perform primary curing at 5 to 80 ° C. for 12 to 30 hours, and the primary curing is more preferably steam curing under normal pressure saturated vapor pressure. Further, in the present invention, additives other than the above-mentioned additives may be used in combination as long as the effects of the present invention are not impaired. Examples thereof include fluidity improvers such as methyl cellulose and polyvinyl alcohol, boric acid compounds such as boric acid, borax, calcium borate and borate esters, water repellents such as calcium stearate,
A foam entraining agent and the like are included.
【0013】[0013]
【実施例】以下に実施例を挙げて本発明をさらに詳しく
説明するが、本発明はこれによって限定されるものでは
ない。なお実施例中とくに断りのないかぎり、「%」お
よび「部」は重量基準を表す。The present invention will be described in more detail with reference to the following examples, but the present invention is not limited thereto. In the examples, "%" and "parts" are based on weight unless otherwise specified.
【0014】[0014]
【評価方法】嵩比重:JIS A5413に準拠し、試
験片を100℃で24時間乾燥後の重量と体積より求め
た。 曲げ強度、曲げたわみ:JIS A1408「建築ボー
ド類の曲げ試験法」に準拠し、スパン長5cmで測定し
た。スパン中央部の最大たわみ量を曲げたわみとする。
曲げたわみが大であるほど成形物が柔軟性を有しており
好ましい。 釘打ち性:3cm角の試料10個のそれぞれの中央部に
釘を打ち破断しなかった個数で表す。[Evaluation method] Bulk specific gravity: Based on JIS A5413, the test piece was obtained from the weight and volume after drying at 100 ° C. for 24 hours. Bending strength and bending deflection: Measured with a span length of 5 cm in accordance with JIS A1408 "Bending test method for building boards". The maximum amount of deflection at the center of the span is the bending deflection.
The larger the bending flexure, the more flexible the molded product is, which is preferable. Nailability: It is represented by the number of nails that were not broken at the center of each of 10 samples of 3 cm square.
【0015】実施例1 ポルトランドセメント48部、珪石粉32部およびパー
ライト15部からなる配合物95部に対して、トウモロ
コシデンプン粉末5部を添加し、混合した粉体を叩解パ
ルプ5部を予め水に離解した分散液に投入撹拌してスラ
リーを抄造後プレス成形して、20℃で24時間の1次
養生した後、160℃で10時間のオートクレーブ養生
をすることにより、無機質成形物を製造した。製造条件
を表1に、物性を表2に示す。併せて、トウモロコシデ
ンプンを添加しない場合を比較例1として表1および表
2に示す。Example 1 5 parts of corn starch powder was added to 95 parts of a mixture consisting of 48 parts of Portland cement, 32 parts of silica stone powder and 15 parts of perlite, and 5 parts of beaten pulp was preliminarily mixed with 5 parts of water. An inorganic molded product was produced by adding the mixture to the dispersion liquid disintegrated and stirring it to form a slurry, press-molding it, and then subjecting it to primary curing at 20 ° C. for 24 hours and then autoclaving at 160 ° C. for 10 hours. . The manufacturing conditions are shown in Table 1 and the physical properties are shown in Table 2. In addition, Table 1 and Table 2 show Comparative Example 1 in the case where corn starch was not added.
【0016】実施例2〜4 実施例1に於いてトウモロコシデンプンを表1の各種デ
ンプン系粉末に変えた以外は、実施例1同様にして成形
物を製造した。製造条件を表1に、物性を表2に示す。Examples 2 to 4 Molded articles were produced in the same manner as in Example 1 except that the starch powder of Table 1 was used instead of the corn starch in Example 1. The manufacturing conditions are shown in Table 1 and the physical properties are shown in Table 2.
【0017】実施例5 実施例1に於いてポリビニルアルコール(クラレ製のP
VA−117:重合度1750、けん化度98.5モル
%)を併用した以外は、実施例1と同様にして成形物を
製造した。製造条件を表1に、物性を表2に示す。Example 5 In Example 1, polyvinyl alcohol (Kuraray P
A molded product was produced in the same manner as in Example 1 except that VA-117: degree of polymerization 1750, degree of saponification 98.5 mol%) was used in combination. The manufacturing conditions are shown in Table 1 and the physical properties are shown in Table 2.
【0018】実施例6 実施例1に於いてほう酸を併用した以外は、実施例1と
同様にして成形物を製造した。製造条件を表1に、物性
を表2に示す。併せて、トウモロコシデンプンを添加し
ない場合を比較例2として表1および表2に示す。Example 6 A molded article was produced in the same manner as in Example 1 except that boric acid was used in combination in Example 1. The manufacturing conditions are shown in Table 1 and the physical properties are shown in Table 2. In addition, Table 1 and Table 2 show Comparative Example 2 in which no corn starch was added.
【0019】比較例3 実施例1に於いてトウモロコシデンプンの添加量を15
部にした以外は、実施例1と同様にして成形物を製造し
た。結果を表1および表2に示す。Comparative Example 3 The amount of corn starch added in Example 1 was 15
A molded product was produced in the same manner as in Example 1 except that the parts were used. The results are shown in Tables 1 and 2.
【0020】[0020]
【表1】 [Table 1]
【0021】[0021]
【表2】 [Table 2]
【0022】実施例7 ポルトランドセメント46部、シリカ(3500ブレー
ン)38部、微粉パーライト12部および叩解パルプ4
部からなるセメント配合物100部に対して、グルコー
ス粉末2部を混合し、混練機を通した後、押出成型機に
て成形した。この成形体を60℃の常圧の飽和水蒸気下
で12時間一次養生した後、160℃で16時間のオー
トクレーブ養生をすることによりセメント成形体を製造
した。製造条件を表3に、物性を表4に示す。Example 7 Portland cement 46 parts, silica (3500 branes) 38 parts, finely divided perlite 12 parts and beaten pulp 4
2 parts of glucose powder was mixed with 100 parts of the cement mixture consisting of 1 part, passed through a kneader, and then molded with an extruder. This molded body was subjected to primary curing for 12 hours under saturated steam at 60 ° C. under normal pressure, and then to 16 hour autoclave curing at 160 ° C. to produce a cement molded body. The manufacturing conditions are shown in Table 3 and the physical properties are shown in Table 4.
【0023】実施例8 実施例7のグルコースに代えて、しょ糖を添加した他
は、実施例7と同様にしてセメント成形体を作成した。
製造条件を表3に、物性を表4に示す。Example 8 A cement molded product was prepared in the same manner as in Example 7, except that sucrose was added instead of glucose in Example 7.
The manufacturing conditions are shown in Table 3 and the physical properties are shown in Table 4.
【0024】実施例9〜16 実施例7と同様にして表3に示した配合量で押し出し成
形した後、一次養生後オートクレーブ養生することによ
り成形体を製造した。製造条件を表3に、物性を表4に
示す。Examples 9 to 16 Extrusion molding was carried out in the same amount as shown in Table 3 in the same manner as in Example 7, followed by primary curing followed by autoclave curing to produce molded products. The manufacturing conditions are shown in Table 3 and the physical properties are shown in Table 4.
【0025】比較例4 実施例7の最終的に混合された組成物をオートクレーブ
養生をする代わりに、高湿度下で常温養生を行ったとこ
ろ、2週後の成形物の強度はほとんど測定できず、十分
な硬化が行われていなかった。Comparative Example 4 When the finally mixed composition of Example 7 was cured at room temperature under high humidity instead of being cured by autoclave, the strength of the molded product after 2 weeks could hardly be measured. , Was not sufficiently cured.
【0026】比較例5 実施例1のグルコースの添加を行わない他は、実施例1
と同様にして成形、オートクレーブ養生をすることによ
りセメント成形物を製造した。製造条件を表3に、物性
を表4に示す。Comparative Example 5 Example 1 was repeated except that glucose was not added in Example 1.
A cement molded product was produced by molding and curing in the same manner as in 1. The manufacturing conditions are shown in Table 3 and the physical properties are shown in Table 4.
【0027】[0027]
【表3】 [Table 3]
【0028】[0028]
【表4】 [Table 4]
【0029】[0029]
【発明の効果】本発明によると、機械的強度に優れ、か
つ釘打ち性などに優れた無機質成形物が得られる。EFFECTS OF THE INVENTION According to the present invention, an inorganic molded article having excellent mechanical strength and nailability can be obtained.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 C04B 24:18 B 14:18 24:02 16:06) Z 103:60 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Internal reference number FI Technical indication C04B 24:18 B 14:18 24:02 16:06) Z 103: 60
Claims (1)
維からなる水硬性配合組成物100重量部に対して、デ
ンプン系化合物、多価アルコール化合物および有機酸塩
からなる群から選ばれた1種または2種以上の添加物を
0.1〜10重量部添加し、均一混合、賦形した後、1
20〜200℃でオートクレーブ養生することを特徴と
する無機質成形物の製造方法。1. One kind selected from the group consisting of starch compounds, polyhydric alcohol compounds and organic acid salts per 100 parts by weight of a hydraulic compounding composition consisting of calcareous powder, siliceous powder and reinforcing fiber, or 0.1 to 10 parts by weight of two or more kinds of additives are added, uniformly mixed and shaped, and then 1
A method for producing an inorganic molded article, which comprises performing autoclave curing at 20 to 200 ° C.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5270538A JPH07126083A (en) | 1993-10-28 | 1993-10-28 | Production of formed inorganic article |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5270538A JPH07126083A (en) | 1993-10-28 | 1993-10-28 | Production of formed inorganic article |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH07126083A true JPH07126083A (en) | 1995-05-16 |
Family
ID=17487599
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP5270538A Pending JPH07126083A (en) | 1993-10-28 | 1993-10-28 | Production of formed inorganic article |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH07126083A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996034839A1 (en) * | 1995-05-04 | 1996-11-07 | Bowman, Paul, Alan | Process for producing insulating materials and products thereof |
JP2000335955A (en) * | 1999-05-28 | 2000-12-05 | Inax Corp | Production of hydrothermally solidified article |
JP2008017223A (en) * | 2006-07-06 | 2008-01-24 | Casio Comput Co Ltd | Imaging apparatus, guide display method of imaging apparatus, and program |
-
1993
- 1993-10-28 JP JP5270538A patent/JPH07126083A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996034839A1 (en) * | 1995-05-04 | 1996-11-07 | Bowman, Paul, Alan | Process for producing insulating materials and products thereof |
JP2000335955A (en) * | 1999-05-28 | 2000-12-05 | Inax Corp | Production of hydrothermally solidified article |
JP2008017223A (en) * | 2006-07-06 | 2008-01-24 | Casio Comput Co Ltd | Imaging apparatus, guide display method of imaging apparatus, and program |
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