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JPS6143317B2 - - Google Patents
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JPS6143317B2 - - Google Patents

Info

Publication number
JPS6143317B2
JPS6143317B2 JP10898780A JP10898780A JPS6143317B2 JP S6143317 B2 JPS6143317 B2 JP S6143317B2 JP 10898780 A JP10898780 A JP 10898780A JP 10898780 A JP10898780 A JP 10898780A JP S6143317 B2 JPS6143317 B2 JP S6143317B2
Authority
JP
Japan
Prior art keywords
silicate
lightweight
aqueous solution
weight
granular
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
Application number
JP10898780A
Other languages
Japanese (ja)
Other versions
JPS5734063A (en
Inventor
Ryuji Nakamura
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.)
SK Kaken Co Ltd
Original Assignee
Shikoku Kaken Industry 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 Shikoku Kaken Industry Co Ltd filed Critical Shikoku Kaken Industry Co Ltd
Priority to JP10898780A priority Critical patent/JPS5734063A/en
Publication of JPS5734063A publication Critical patent/JPS5734063A/en
Publication of JPS6143317B2 publication Critical patent/JPS6143317B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】 本発明は、諸性能の優れた軽量体組成物に係
り、詳しくは、該軽量体の発泡硬化速度が所望の
軽量体を得ようとするに適しく調整された組成物
に関するものである。 本発明者らは、以前よりアルカリ硅酸塩の結合
力並びに不燃性能等の特性を生かして軽量体を得
る研究に従事しており、既に耐水性、圧縮強度、
耐衝撃性などの優れた発泡硬化型の軽量体を創作
してきた。しかしながら、それらは概ね発泡硬化
の時間が短かいために混合ペーストの輸送に時間
がかかり、又、殊に気温の高い場所では発泡硬化
が極端に早くなつて作業上の支障を来たしてい
た。 本発明者らは係る発泡硬化型の軽量体を得るに
際し、種々発泡もしくは硬化を調整する手段を講
じてきたが、ここに軽量体自体の性能を損うこと
なく、発泡硬化の時間を調整し得る組成物を完成
するに到つたものである。即ち、本発明は、一般
式R2O・nSiO2(但し、Rはアルカリ金属又は第
四級アンモニウム、nは1.5〜7.0の正数)で示さ
れる硅酸塩の水溶液、該硅酸塩水溶液の硬化性成
分、粒状軽量材及び次亜塩素酸塩、塩素酸塩、過
塩素酸塩から選ばれる一種の塩単独又は該塩に硅
酸塩を配合した水溶液で前処理した金属粉末から
成る軽量体組成物を提供するものであり、このよ
うな組成物は発泡硬化の際の時間がかなり調整し
やすく、又注形もしくは塗付などの方法によつて
得られる軽量体の圧縮強さもある程度向上するこ
とがわかつた。以下、本発明の各々の成分につき
詳述する。 本発明に用いる硅酸塩の水溶液とは上述のごと
きSiO2/R2Oモル比が1.5〜7.0の範囲にあるアル
カリ硅酸塩で、使用形態は水溶液状を呈し通常水
ガラスと称呼されている。次に、該硅酸塩水溶液
の硬化性成分は、通常水ガラスの硬化剤として使
用されるものが使用でき、フツ化物、硅フツ化
物、リン酸塩、ホウ酸塩、セメント、酸化亜鉛、
亜硫酸カルシウムなどを例示できる。更に、粒状
軽量材とは、有機質、無機質の材質を問わず使用
できるもので例えば塩化ビニル、フエノール、ユ
リア、スチレン、ウレタン、エチレン等の合成樹
脂の粒状発泡体もしくは粒状粉砕物、合成ゴムの
粒状発泡体や粉砕物のごとき有機質軽量材、ヒル
石、膨脹頁岩、パーライト、シリカバルーン、粒
状発泡シリカ等の無機質発泡体、この他無機質人
工軽量骨材やALCの粉砕物などを掲げることが
できる。更に又、前処理した金属粉末の金属と
は、Al、Mg、Mn、Co、Ca、Sn、Mo、Sb等の
いわゆる両性金属単独もしくはそれらを含む合金
であればよく、又金属硅素、シリコマグネシウ
ム、フエロシリコン等の硅素合金も使用できる。
軽量体の組成物調整に当つてはこれら金属粉末を
前処理するのであるが、前処理剤として用いるも
のは、次亜塩素酸ナトリウム、次亜塩素酸カリウ
ム等の次亜塩素酸塩、塩素酸ナトリウム、塩素酸
カリウム等の塩素酸塩、過塩素酸ナトリウム、過
塩素酸カリウム等の過塩素酸塩から選ばれる一種
の塩の水溶液であり、これに必要に応じてアルカ
リ硅酸塩水溶液又はコロイダルシリカを添加配合
することができる。係る前処理剤の前処理に際し
ては濃度の調整が重要で、前記塩素含有塩の場合
は約0.01〜12%、望ましくは約0.01〜8%が良
く、アルカリ硅酸塩の場合は、約0.5〜25%が望
ましい。このような前処理の実施態様を具体的に
例示すると、予め前処理剤の液を調整し、次に金
属粉末を徐々に撹拌しながら混合し、常温下で
0.5〜30分、加温下の場合はもつと短い時間で処
理せしめ、処理後過、水洗、乾燥する。この他
本発明組成物には各種副目的により界面活性剤や
無機質顔料、無機質の各種体質顔料、添加剤など
を適宜配合できる。 本発明は上述のごとき組成物より成るものであ
るが、その配合比は硅酸塩水溶液の固形分100重
量部に対して該硅酸塩水溶液の硬化性成分約1〜
50重量部、粒状軽量材を約5〜100重量部、前処
理金属粉末を約1〜20重量部配合するものであ
る。 このようにして得られる本発明組成物の固体形
成物は注形によつてもしくは塗付によつて、該組
成物の発泡硬化機構により乾燥工程を経て見られ
るものであるが、その作用構成は不明であるにせ
よ、耐水性、耐アルカリ性が非常に良好で、且つ
各種下地への付着性が良く、軽量体を得るに際
し、発泡硬化をよく制御できるために輸送に際し
て管内での固化がなく、又高温にさらされても適
当なポツトライフを有しているので作業上支障が
なく、予想外なことには軽量体の圧縮強度が若干
向上することが分かつたことである。 以下実施例を示す。 実施例 予め、塩素酸カリウムが3重量%、硅酸ナトリ
ウム(SiO2/Na2Oモル比3.9)が17重量%になる
ように処理用水溶液を調整し、この処理液100g
の中に、Al粉末を20g加えて35℃で各々の時間前
処理し(実験1〜5)過、水洗、乾燥を経て、
前処理Al粉末を得た。次に、Na2O・3.1SiO2から
成るアルカリ金属硅酸塩水溶液(固形分40重量
%)100重量部に硅フツ化ナトリウム5重量部、
比重0.2の発泡ヒル石(10〜24メツシユ)10重量
部及び上記前処理Al粉末5重量部配合し、約1
分間撹拌した後300×300×15mmの型枠に注入し、
約20℃の室内で発泡開始時間を測定したところ、
第1表に示すような結果になつた。又、この成形
板を用いて、圧縮強さ試験を行つた所、その結果
は第1表に示すようなものであつた。 【表】
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a lightweight body composition with excellent performance, and more particularly, to a composition in which the foam curing speed of the lightweight body is adjusted to suit the purpose of obtaining a desired lightweight body. It is about things. The present inventors have been engaged in research for some time to obtain a lightweight body by taking advantage of the properties of alkali silicates such as their binding strength and nonflammability, and have already achieved water resistance, compressive strength,
We have created lightweight, foam-hardened bodies with excellent impact resistance. However, since the time for foaming and hardening is generally short, it takes time to transport the mixed paste, and the foaming and hardening occurs extremely quickly, especially in places with high temperatures, causing problems in work. The inventors of the present invention have taken various measures to adjust the foaming or curing process in order to obtain such a foam-hardening lightweight body. The resulting composition has now been completed. That is, the present invention provides an aqueous solution of a silicate represented by the general formula R 2 O.nSiO 2 (where R is an alkali metal or quaternary ammonium, and n is a positive number from 1.5 to 7.0), and an aqueous solution of the silicate. A lightweight material consisting of a curable component, a granular lightweight material, and a metal powder pretreated with a salt selected from hypochlorites, chlorates, and perchlorates, or an aqueous solution containing the salt and a silicate. The foam curing time of such compositions can be easily adjusted, and the compressive strength of lightweight bodies obtained by methods such as casting or painting can be improved to some extent. I found out what to do. Each component of the present invention will be explained in detail below. The aqueous solution of silicate used in the present invention is an alkali silicate having a molar ratio of SiO 2 /R 2 O in the range of 1.5 to 7.0 as described above, and is used in the form of an aqueous solution and is usually called water glass. There is. Next, the hardening components of the silicate aqueous solution can be those commonly used as hardening agents for water glass, such as fluorides, fluorosilicates, phosphates, borates, cement, zinc oxide,
Examples include calcium sulfite. Furthermore, granular lightweight materials can be used regardless of organic or inorganic materials, such as granular foams or granular crushed products of synthetic resins such as vinyl chloride, phenol, urea, styrene, urethane, and ethylene, and granular particles of synthetic rubber. Organic lightweight materials such as foams and crushed materials, inorganic foams such as vermiculite, expanded shale, perlite, silica balloons, and granular foamed silica, as well as other inorganic artificial lightweight aggregates and crushed materials of ALC, etc. can be listed. Furthermore, the metal of the pretreated metal powder may be a so-called amphoteric metal such as Al, Mg, Mn, Co, Ca, Sn, Mo, Sb alone or an alloy containing them, and metal silicon, silicomagnesium, etc. , silicon alloys such as ferrosilicon can also be used.
These metal powders are pretreated when preparing the composition of the lightweight body, and the pretreatment agents used include hypochlorites such as sodium hypochlorite and potassium hypochlorite, and chloric acid. It is an aqueous solution of a kind of salt selected from chlorates such as sodium and potassium chlorate, and perchlorates such as sodium perchlorate and potassium perchlorate, and if necessary, an aqueous alkali silicate solution or colloidal Silica can be added and blended. It is important to adjust the concentration when pre-treating such a pre-treatment agent; in the case of the chlorine-containing salts, it is about 0.01 to 12%, preferably about 0.01 to 8%, and in the case of alkali silicates, it is about 0.5 to 12%. 25% is desirable. To give a concrete example of such a pretreatment, a pretreatment agent liquid is prepared in advance, then the metal powder is gradually mixed with stirring, and then the mixture is heated at room temperature.
Treat for 0.5 to 30 minutes, or even shorter if heated, and then filter, wash with water, and dry. In addition, surfactants, inorganic pigments, various inorganic extender pigments, additives, and the like may be appropriately blended into the composition of the present invention depending on various subpurposes. The present invention consists of the composition as described above, and the blending ratio is about 1 to 100 parts by weight of the curable component of the silicate aqueous solution to 100 parts by weight of the solid content of the silicate aqueous solution.
50 parts by weight, about 5 to 100 parts by weight of granular lightweight material, and about 1 to 20 parts by weight of pretreated metal powder. The solid formed product of the composition of the present invention obtained in this way can be seen through a drying process by casting or coating, using the foaming hardening mechanism of the composition, but its working structure is Although it is unknown, it has very good water resistance and alkali resistance, and has good adhesion to various substrates, and when obtaining a lightweight body, foam hardening can be well controlled, so it does not solidify in the pipe during transportation. In addition, it has a suitable pot life even when exposed to high temperatures, so there is no problem in working with it, and unexpectedly it has been found that the compressive strength of lightweight bodies is slightly improved. Examples are shown below. Example An aqueous treatment solution was prepared in advance so that potassium chlorate was 3% by weight and sodium silicate (SiO 2 /Na 2 O molar ratio 3.9) was 17% by weight, and 100 g of this treatment solution was prepared.
20g of Al powder was added to the mixture, pretreated at 35°C for various times (Experiments 1 to 5), filtered, washed with water, and dried.
Pretreated Al powder was obtained. Next, 5 parts by weight of sodium fluorosilicate were added to 100 parts by weight of an aqueous alkali metal silicate solution (solid content 40% by weight) consisting of Na 2 O.3.1SiO 2 .
10 parts by weight of foamed vermiculite (10 to 24 mesh) with a specific gravity of 0.2 and 5 parts by weight of the above pretreated Al powder were mixed, and approximately 1
After stirring for a minute, pour it into a 300 x 300 x 15 mm mold.
When we measured the foaming start time in a room at about 20℃,
The results are as shown in Table 1. In addition, a compressive strength test was conducted using this molded plate, and the results were as shown in Table 1. 【table】

Claims (1)

【特許請求の範囲】[Claims] 1 一般式R2O・nSiO2(但し、Rはアルカリ金
属又は第四級アンモニウム、nは1.5〜7.0の正
数)で示される硅酸塩の水溶液、該硅酸塩水溶液
の硬化性成分、粒状軽量材及び次亜塩素酸塩、塩
素酸塩、過塩素酸塩から選ばれる1種の塩単独又
は該塩に硅酸塩を配合した水溶液で前処理した金
属粉末から成る軽量体組成物。
1 An aqueous solution of a silicate represented by the general formula R 2 O・nSiO 2 (wherein R is an alkali metal or quaternary ammonium, and n is a positive number from 1.5 to 7.0), a curable component of the aqueous silicate solution, A lightweight body composition comprising a granular lightweight material and a metal powder pretreated with an aqueous solution of one kind of salt selected from hypochlorites, chlorates, and perchlorates or a mixture of the salt and a silicate.
JP10898780A 1980-08-07 1980-08-07 Lightweight body composition Granted JPS5734063A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10898780A JPS5734063A (en) 1980-08-07 1980-08-07 Lightweight body composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10898780A JPS5734063A (en) 1980-08-07 1980-08-07 Lightweight body composition

Publications (2)

Publication Number Publication Date
JPS5734063A JPS5734063A (en) 1982-02-24
JPS6143317B2 true JPS6143317B2 (en) 1986-09-26

Family

ID=14498708

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10898780A Granted JPS5734063A (en) 1980-08-07 1980-08-07 Lightweight body composition

Country Status (1)

Country Link
JP (1) JPS5734063A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS627681A (en) * 1985-07-01 1987-01-14 日本軽金属株式会社 Manufacture of inorganic heat insulator
CN106242387A (en) * 2016-07-18 2016-12-21 柳州弘蓝科技有限公司 The method being raw material production heat-preservation building blocks with multiple holes with shale

Also Published As

Publication number Publication date
JPS5734063A (en) 1982-02-24

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