JPH0375511B2 - - Google Patents
Info
- Publication number
- JPH0375511B2 JPH0375511B2 JP57055579A JP5557982A JPH0375511B2 JP H0375511 B2 JPH0375511 B2 JP H0375511B2 JP 57055579 A JP57055579 A JP 57055579A JP 5557982 A JP5557982 A JP 5557982A JP H0375511 B2 JPH0375511 B2 JP H0375511B2
- Authority
- JP
- Japan
- Prior art keywords
- cement
- foam
- calcareous
- component
- 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.)
- Expired - Lifetime
Links
Landscapes
- Porous Artificial Stone Or Porous Ceramic Products (AREA)
Description
【発明の詳細な説明】
本発明は発泡体製造用組成物に関し、詳しくは
常温下で安定に発泡硬化し得る機械的強度の優れ
たセメント系発泡体を得る所に特徴がある。
以前より本発明者らは、可溶性硅酸アルカリに
セメントや酸化亜鉛などのような前記成分の硬化
性成分及び特定の発泡安定剤を主要構成成分と
し、これを金属系発泡剤を介して発泡硬化せしめ
て無機質の発泡体を得てきた。係る発泡体製造技
術によつて従来現場発泡形の材料の使用が困難と
されていた建築や築炉の各用途への使用が可能と
なつたばかりではなく、その成分や構造の特異性
などによつて各産業用途にも種々応用されてい
る。しかしながら、可溶性硅酸アルカリを必須成
分として用いているために使用上色々な制限を受
けることもあり、例えば低い温度下での発泡硬化
のタイミング調整などに問題が残されていた。
このような事情に鑑み本発明者らは上述発泡体
の構成成分の内、特に各配合成分が付与する発泡
体製造に際しての機能を究明し続けて来た。とり
わけ、可溶性硅酸アルカリの成分に着目して研究
を続けてきた結果、これを水酸化アルカリ金属と
高硅酸質粉体に分割して発泡体製造の実験をした
宿、意外にも夫々特定の配合比率に調整した場合
にのみ良好な発泡体が得られることが分かり、こ
こに本発明を完成するに至つた。即ち、本発明は
(a)硅酸石灰質セメントとアルミン酸石灰質セメン
トとの混合セメント(以下(a)成分という)、(b)水
酸化アルカリ金属(以下(b)成分という)、(c)高硅
酸質粉体(以下(c)成分という)、及び(d)金属系発
泡剤(以下(d)成分という)を主要構成成分とし、
これに水を加えて一たんペースト状に調整して発
泡体を製造するものである。以下、各々の成分に
ついて詳述する。
(a)成分は前述したごとく硅酸石灰質セメントと
アルミン酸石灰質セメントとの混合セメントで、
硅酸セメントと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、中庸熱ポルトランドセ
メント、シリカセメント、高硫酸塩スラグセメン
ト、フアイアツシユセメント、石灰スラグセメン
トのような単味又は混合の水硬性セメントをい
う。この硅酸石灰質セメントに対してアルミン酸
石灰質セメント、即ちアルミナセメントを配合し
たものである。しかし、アルミナセメント単味の
時又はその量があまりに多い時には硬化反応が先
行して望ましい発泡体が得られないので、その混
合比率は硅酸石灰質セメント100重量部に対して
300重量部以内とするものである。次に(b)成分は
LiOH、NaOH、KOHのようなアルカリ金属の
水酸化物をいうものであり、発泡体製造に際して
は粉体、フレーク状又は水溶液の形態何れでも構
わない。(c)成分はその構成成分中に少なくとも70
重量%のSiO2を含有する高硅酸質の粉体をいい、
硅そう土、硅石、硅砂、硅華などの天然鉱物、電
熱や金法による硅素合金製造の際に副生されるシ
リカダスト、及び化学品としてシリカゲル、ホワ
イトカーボンのようなものが例示できる。これら
は粉体の形態で用いる。(d)成分は、単体金属、合
金及び金属間化合物などアルカリ水溶液中で気泡
を発生するものがこれに含まれる。
本発明は以上の(a)〜(d)成分を必須成分とし、こ
れに水を配合することによつて無機質の発泡体を
製造し得るもので、その配合比率は(a)成分100重
量部に対して、(b)成分2〜150重量部程度、(c)成
分5〜250重量部程度及び(d)成分0.1〜10重量部程
度とし、この内特に(b)成分と(c)成分とは式
SiO2/R2O(但しRはアルカリ金属)で表わされ
るモル比が1.0〜5.0の範囲内であることが重要で
あつて、係るモル比がどちらかに外れる場合には
望ましい発泡体を得難い。また(b)成分と(c)成分の
合計配合量は(a)成分100重量部に対して7〜350重
量部程度とするものである。以上の(a)〜(d)成分を
配合して発泡体を得るに際しては、予め(a)、(c)及
び(d)成分から成る混合粉体を調整しておき、この
混合粉体と(b)成分の水溶液を混合攪拌してペース
ト状にする場合が最も容易である。無論(a)+(d)成
分の粉体系に、(b)+(c)成分の溶液系を混合するこ
とも可能であり、係る調合手段によつて本発明組
成物の反応性状や発泡体性能に格別に支障を与え
るものではない。一たんペースト状に調整された
組成物は、徐々に発泡を開始しながら硬化反応を
併起して発泡体を形成していく。発泡を開始して
から遅くとも24時間以内には軽量で硬い発泡体が
でき上り、この発泡体は断熱性が優れる。特筆す
べきは、係る組成物は極めて低い温度下において
発泡硬化反応が比較的スムースに進行し、この点
今までの発泡体を製造するための組成物とはその
性状を異にする所である。本発明組成物は、上記
(a)〜(d)成分より成るが、機械的強度や断熱性等を
向上する目的で、所謂発泡安定剤を配合すること
ができ、係る発泡安定剤として有効なものは、ゼ
オライト、カーボンブラツク、活性炭のような多
孔性無機質粉末、又マイカ、タルク、セピオライ
ト、パリゴルスカイトのような層状構造を有する
鉱物粉、更には極く少量使用できるものとして界
面活性剤を例示することができる。一方、本発明
組成物は上述必須成分の他に、充てん材あるいは
強度向上材として無機質繊維や軽量骨材、水溶性
高分子、合成高分子の水分散液、酸化亜鉛、リン
酸塩なども本発明の発泡硬化反応に支障のない限
り使用できるものである。以下本発明を実施例に
より詳述する。
実施例 1
普通ポルトランドセメント80g、アルミナセメ
ント20g、シリカダスト50g及び金属アルミニウ
ム粉5gを、1ポリエチレン容器に採取しよく
混合する。一方、水酸化カリウム25gを水75g中
に溶解して得た水酸化カリウム水溶液を上記混合
粉体に混入しよく攪拌混合する。これを迅速に5
℃の定温恒温器に置いて外部から観察する。混合
物は40分後に発泡を開始し初め、4.5時間後には
硬化を終了して発泡体が得られた。この発泡体の
かさ比重は0.27で、圧縮強度は4.9Kg/cm2であつ
た。
実施例 2
実施例1において、各成分を第1表に示す配合
にして適宜水を加えた以外は実施例1と同じ方法
で発泡体を得た。これらの発泡体について、実施
例1と同じ試験を行つた所第1表に示す結果が得
られた。
比較例 1〜2
実施例1において、各成分を第1表に示す配合
にし適宜水を加えた以外は実施例1と同じ方法で
発泡体を得た。これらの発泡体について、実施例
1と同じ試験を行つた所第1表に示す結果が得ら
れた。
【表】DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a composition for producing a foam, and is particularly characterized in that it provides a cement foam with excellent mechanical strength that can be stably foamed and hardened at room temperature. Previously, the present inventors have used soluble alkali silicate as main components, hardening components such as cement and zinc oxide, and a specific foaming stabilizer, and foamed and hardened this through a metal foaming agent. At least we have obtained an inorganic foam. This foam manufacturing technology has not only made it possible to use foam-in-place materials in various applications such as construction and furnace construction, where it was difficult to use conventional materials, but also because of the uniqueness of their components and structure. Therefore, it is also applied to various industrial applications. However, since it uses soluble alkali silicate as an essential component, it is subject to various limitations in use, and problems remain, for example, in adjusting the timing of foaming and curing at low temperatures. In view of these circumstances, the present inventors have continued to investigate, among the constituent components of the above-mentioned foam, especially the functions imparted by each compounded component during the production of the foam. In particular, as a result of continuing research focusing on the components of soluble alkali silicate, it was surprisingly identified that an experiment was carried out to produce foam by dividing it into alkali metal hydroxide and high-silicate powder. It was found that a good foam could be obtained only when the blending ratio was adjusted to , and the present invention was thus completed. That is, the present invention
(a) Mixed cement of calcareous silicate cement and calcareous aluminate cement (hereinafter referred to as (a) component), (b) alkali metal hydroxide (hereinafter referred to as (b) component), (c) high silicate powder (hereinafter referred to as (c) component), and (d) metallic foaming agent (hereinafter referred to as (d) component) as the main components,
A foam is produced by adding water to the mixture and making it into a paste. Each component will be explained in detail below. As mentioned above, component (a) is a mixed cement of silicate calcareous cement and aluminate calcareous cement.
Silicate cement refers to single or mixed hydraulic cements such as ordinary Portland cement, early strength Portland cement, moderate heat Portland cement, silica cement, high sulfate slag cement, fire ash cement, and lime slag cement. This calcareous silicate cement is blended with a calcareous aluminate cement, that is, alumina cement. However, when alumina cement is used alone or in too large a quantity, the curing reaction takes place and the desired foam cannot be obtained.
The amount shall be within 300 parts by weight. Next, component (b) is
It refers to an alkali metal hydroxide such as LiOH, NaOH, and KOH, and when producing foam, it may be in the form of powder, flakes, or an aqueous solution. (c) the component contains at least 70% in its constituent parts;
Highly silicic acid powder containing % by weight of SiO2 ,
Examples include natural minerals such as silica earth, silica stone, silica sand, and silica flowers, silica dust by-produced during the production of silicon alloys by electric heating or metallurgy, and chemical products such as silica gel and white carbon. These are used in powder form. Component (d) includes those that generate bubbles in an alkaline aqueous solution, such as simple metals, alloys, and intermetallic compounds. The present invention uses the above components (a) to (d) as essential components, and by blending them with water, an inorganic foam can be produced, and the blending ratio is 100 parts by weight of component (a). Component (b) should be about 2 to 150 parts by weight, component (c) should be about 5 to 250 parts by weight, and component (d) should be about 0.1 to 10 parts by weight, especially the (b) and (c) components. is the expression
It is important that the molar ratio expressed by SiO 2 /R 2 O (where R is an alkali metal) is within the range of 1.0 to 5.0; if the molar ratio is outside the range, it will be difficult to obtain a desired foam. . The total amount of components (b) and (c) is about 7 to 350 parts by weight per 100 parts by weight of component (a). When blending the above components (a) to (d) to obtain a foam, a mixed powder consisting of components (a), (c), and (d) is prepared in advance, and this mixed powder and The easiest method is to mix and stir an aqueous solution of component (b) to form a paste. Of course, it is also possible to mix a solution system of components (b) + (c) with a powder system of components (a) + (d), and by such a preparation method, the reaction properties of the composition of the present invention and the foam can be changed. It does not particularly impede performance. Once the composition has been prepared into a paste, it gradually starts foaming and undergoes a curing reaction to form a foam. A lightweight, hard foam is produced within 24 hours at the latest from the start of foaming, and this foam has excellent thermal insulation properties. What is noteworthy is that the foaming and curing reaction of this composition proceeds relatively smoothly at extremely low temperatures, and in this respect its properties are different from those of conventional compositions for producing foams. . The composition of the present invention has the above-mentioned properties.
It consists of components (a) to (d), but a so-called foaming stabilizer can be added for the purpose of improving mechanical strength, heat insulation, etc. Effective foaming stabilizers include zeolite, carbon black, etc. , porous inorganic powders such as activated carbon, mineral powders having a layered structure such as mica, talc, sepiolite, and palygorskite, and surfactants that can be used in extremely small amounts. On the other hand, in addition to the above-mentioned essential components, the composition of the present invention also contains inorganic fibers, lightweight aggregates, water-soluble polymers, aqueous dispersions of synthetic polymers, zinc oxide, phosphates, etc. as fillers or strength-improving materials. It can be used as long as it does not interfere with the foam curing reaction of the invention. The present invention will be explained in detail below with reference to Examples. Example 1 80 g of ordinary Portland cement, 20 g of alumina cement, 50 g of silica dust, and 5 g of metal aluminum powder were collected in a polyethylene container and mixed well. On the other hand, a potassium hydroxide aqueous solution obtained by dissolving 25 g of potassium hydroxide in 75 g of water is mixed into the above mixed powder and mixed with thorough stirring. Do this quickly 5
Place in a constant temperature incubator at ℃ and observe from the outside. The mixture started foaming after 40 minutes, and curing was completed after 4.5 hours to obtain a foam. This foam had a bulk specific gravity of 0.27 and a compressive strength of 4.9 Kg/cm 2 . Example 2 A foam was obtained in the same manner as in Example 1, except that each component was formulated as shown in Table 1 and water was added as appropriate. When these foams were subjected to the same tests as in Example 1, the results shown in Table 1 were obtained. Comparative Examples 1 to 2 A foam was obtained in the same manner as in Example 1, except that each component was formulated as shown in Table 1 and water was added as appropriate. When these foams were subjected to the same tests as in Example 1, the results shown in Table 1 were obtained. 【table】
Claims (1)
セメントとの混合セメント100重量部に対し、 (b) 水酸化アルカリ金属2〜150重量部、 (c) 高硅酸質粉体5〜250重量部、及び、 (d) 金属系発泡剤0.1〜10重量部 並びに水から成る発泡体製造用組成物。 2 混合セメントにおける硅酸石灰質セメントと
アルミン酸石灰質セメントの比率が、1:3以下
である特許請求の範囲第1項に記載の発泡体製造
用組成物。 3 水酸化アルカリ金属中のアルカリ金属酸化物
1モルに対し、高硅酸質粉体中の硅酸が1.0〜5.0
モル調整されて配合される特許請求の範囲第1項
に記載の発泡体製造用組成物。 4 更に発泡安定剤が配合されて成る特許請求の
範囲第1項に記載の発泡体製造用組成物。[Scope of Claims] 1 (a) 100 parts by weight of mixed cement of calcareous silicate cement and calcareous aluminate cement, (b) 2 to 150 parts by weight of alkali metal hydroxide, (c) high silica powder (d) 0.1 to 10 parts by weight of a metal blowing agent and water. 2. The composition for producing a foam according to claim 1, wherein the ratio of calcareous silicate cement and calcareous aluminate cement in the mixed cement is 1:3 or less. 3 The amount of silicic acid in the high silicic acid powder is 1.0 to 5.0 per mole of alkali metal oxide in the alkali metal hydroxide.
The composition for producing a foam according to claim 1, which is blended in a molar adjusted manner. 4. The composition for producing a foam according to claim 1, further comprising a foam stabilizer.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5557982A JPS58172258A (en) | 1982-04-03 | 1982-04-03 | Foamed body manufacturing composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5557982A JPS58172258A (en) | 1982-04-03 | 1982-04-03 | Foamed body manufacturing composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS58172258A JPS58172258A (en) | 1983-10-11 |
| JPH0375511B2 true JPH0375511B2 (en) | 1991-12-02 |
Family
ID=13002642
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5557982A Granted JPS58172258A (en) | 1982-04-03 | 1982-04-03 | Foamed body manufacturing composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS58172258A (en) |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS51130422A (en) * | 1975-05-08 | 1976-11-12 | Asahi Chemical Ind | Manufacturing of light foamed concrete |
| JPS5442373A (en) * | 1977-09-12 | 1979-04-04 | Tokuyama Soda Co Ltd | Clamping type gasket for electrolytic cell |
-
1982
- 1982-04-03 JP JP5557982A patent/JPS58172258A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS58172258A (en) | 1983-10-11 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA1065901A (en) | Process for preparing a foamed body | |
| JP5730325B2 (en) | Inorganic binder systems for the production of chemically resistant building chemicals | |
| EP3262008B1 (en) | Particulate compositions for the formation of geopolymers, their use and methods for forming geopolymers therewith | |
| US4030939A (en) | Cement composition | |
| CN104395263B (en) | Form the inorganic foamed method of quick-hardening | |
| JPH0218314B2 (en) | ||
| US2914413A (en) | Cement composition and method of preparation | |
| WO1985000359A1 (en) | Cementitious composite material | |
| JPH06503798A (en) | Method for producing microporous foam consisting primarily of inorganic components | |
| JP3174050B2 (en) | Kit of molding material and components for producing molded article, and molded article | |
| US9957197B1 (en) | Porous geopolymers | |
| US7354542B1 (en) | Lightweight, heat insulating, high mechanical strength shaped product and method of producing the same | |
| JP2000178065A (en) | Curable inorganic composition and method for producing inorganic molded article | |
| JPS5926957A (en) | Manufacture of calcium silicate hydrate hardened body | |
| JPH0375511B2 (en) | ||
| WO1993016965A1 (en) | Geopolymeric binder material | |
| JP2881511B2 (en) | Composition for inorganic foam | |
| JP7757226B2 (en) | Geopolymer composition and its hardened product | |
| JPS6149272B2 (en) | ||
| JPS6149273B2 (en) | ||
| JPH0637336B2 (en) | Manufacturing method of inorganic foam | |
| JP2000159582A (en) | Inorganic foam cured body | |
| JPH0323507B2 (en) | ||
| JPH02120255A (en) | Production of foamed inorganic glass | |
| JP2006111485A (en) | Setting accelerator for cement and cement composition |