JPS6025394B2 - inorganic composition - Google Patents
inorganic compositionInfo
- Publication number
- JPS6025394B2 JPS6025394B2 JP15245180A JP15245180A JPS6025394B2 JP S6025394 B2 JPS6025394 B2 JP S6025394B2 JP 15245180 A JP15245180 A JP 15245180A JP 15245180 A JP15245180 A JP 15245180A JP S6025394 B2 JPS6025394 B2 JP S6025394B2
- Authority
- JP
- Japan
- Prior art keywords
- component
- water
- foam
- composition
- powder
- 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
Links
- 239000000203 mixture Substances 0.000 title claims description 19
- 239000000843 powder Substances 0.000 claims description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 9
- 238000005187 foaming Methods 0.000 claims description 7
- 229910052910 alkali metal silicate Inorganic materials 0.000 claims description 6
- 229910001593 boehmite Inorganic materials 0.000 claims description 6
- FAHBNUUHRFUEAI-UHFFFAOYSA-M hydroxidooxidoaluminium Chemical compound O[Al]=O FAHBNUUHRFUEAI-UHFFFAOYSA-M 0.000 claims description 6
- INJRKJPEYSAMPD-UHFFFAOYSA-N aluminum;silicic acid;hydrate Chemical compound O.[Al].[Al].O[Si](O)(O)O INJRKJPEYSAMPD-UHFFFAOYSA-N 0.000 claims description 4
- 239000010443 kyanite Substances 0.000 claims description 4
- 229910052850 kyanite Inorganic materials 0.000 claims description 4
- -1 diaspo Inorganic materials 0.000 claims description 3
- 239000004088 foaming agent Substances 0.000 claims description 3
- 229910052851 sillimanite Inorganic materials 0.000 claims description 3
- 239000004480 active ingredient Substances 0.000 claims description 2
- 229910001679 gibbsite Inorganic materials 0.000 claims description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 2
- 239000011707 mineral Substances 0.000 claims description 2
- 239000006260 foam Substances 0.000 description 16
- 229910052751 metal Inorganic materials 0.000 description 12
- 239000002184 metal Substances 0.000 description 9
- 150000002739 metals Chemical class 0.000 description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 229910017758 Cu-Si Inorganic materials 0.000 description 2
- 229910017931 Cu—Si Inorganic materials 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 230000005856 abnormality Effects 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 229910000272 alkali metal oxide Inorganic materials 0.000 description 2
- 239000010425 asbestos Substances 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 238000012669 compression test Methods 0.000 description 2
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 229910000765 intermetallic Inorganic materials 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 229910052895 riebeckite Inorganic materials 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- 229910017082 Fe-Si Inorganic materials 0.000 description 1
- 229910017133 Fe—Si Inorganic materials 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 229910014299 N-Si Inorganic materials 0.000 description 1
- 229910014291 N—Cu Inorganic materials 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 241000124033 Salix Species 0.000 description 1
- 238000003723 Smelting Methods 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 1
- 229910007609 Zn—S Inorganic materials 0.000 description 1
- 229910007610 Zn—Sn Inorganic materials 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910001583 allophane Inorganic materials 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 229910001570 bauxite Inorganic materials 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- PASHVRUKOFIRIK-UHFFFAOYSA-L calcium sulfate dihydrate Chemical compound O.O.[Ca+2].[O-]S([O-])(=O)=O PASHVRUKOFIRIK-UHFFFAOYSA-L 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000004568 cement Chemical class 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 229910052733 gallium Inorganic materials 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 229910001710 laterite Inorganic materials 0.000 description 1
- 239000011504 laterite Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 229910001092 metal group alloy Inorganic materials 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011490 mineral wool Substances 0.000 description 1
- 239000013518 molded foam Substances 0.000 description 1
- 229910052755 nonmetal Inorganic materials 0.000 description 1
- 150000002843 nonmetals Chemical class 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 239000010451 perlite Substances 0.000 description 1
- 235000019362 perlite Nutrition 0.000 description 1
- 125000002467 phosphate group Chemical class [H]OP(=O)(O[H])O[*] 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000011505 plaster Substances 0.000 description 1
- 239000002984 plastic foam Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000011802 pulverized particle Substances 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 239000011819 refractory material Substances 0.000 description 1
- 229910052701 rubidium Inorganic materials 0.000 description 1
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000010454 slate Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000010455 vermiculite Substances 0.000 description 1
- 229910052902 vermiculite Inorganic materials 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 235000014692 zinc oxide Nutrition 0.000 description 1
Landscapes
- Curing Cements, Concrete, And Artificial Stone (AREA)
- Porous Artificial Stone Or Porous Ceramic Products (AREA)
Description
【発明の詳細な説明】
本発明は、発泡性を有する組成物に関し、詳しくは、常
温又は加温下で原料物質を水と共に混練するだけで発泡
体を製造し得る組成物に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a composition having foaming properties, and more particularly to a composition that can produce a foam simply by kneading raw materials with water at room temperature or under heating.
従来より、水可溶性アルカリ桂酸塩を主要成分とする無
機質発泡体製造技術に関しては既に公知であり、例えば
(a、発泡性を用いることなく加熱下において水蒸気の
発生をもって発泡体を得るもの、あるし・は(b}金属
粉体を加えてカスを発生させ発泡体を得るもの等がある
が、いずれの場合も水可溶性アルカリ桂酸塩を水溶液の
形で用いており、発泡体の物性を維持するためには硬化
剤の添加は不可欠のことであり、通常用いられる硬化剤
として、金属の酸性塩、セメント類、石こう等の水硬性
物質、二価以上の金属の酸化物、水酸化物等が使用され
ていた。しかしながら、従来からの硬化剤は水可溶性ア
ルカリ桂酸塩との硬化反応が敏感であり、配合量の変化
が直ちに反応速度に影響を与える一方、発泡体の強度、
耐久性を良くしようとすれば必然的に硬化剤の配合量を
多くしなければならずそれがため硬化速度が速くなって
該組成物の可便時間を短くし、作業を困難ならしめると
いう欠点があった。又反応速度が大きくなるに伴い発泡
体内部における収縮歪みが大きくなりクラック発生が生
ずるという欠点をも有していた。本発明は従来からの硬
化剤に変え、硬化性成分として全く新規な鉱物の粉体及
び/又は赤泥を用いることにその特徴があり、係る硬化
性成分は水可溶性アルカリ桂酸塩との硬化機能を有して
いるが、その反応速度は緩慢であり、配合量の変化に対
しても反応速度に敏感には影響しないという性質を有し
ていることを本発明者らが初めて知見した。Conventionally, techniques for producing inorganic foams containing water-soluble alkali silicate as a main component have already been known. (b) There are methods to obtain foam by adding metal powder to generate scum, but in all cases, water-soluble alkali silicate is used in the form of an aqueous solution, and the physical properties of the foam cannot be improved. The addition of a hardening agent is essential to maintain this property, and commonly used hardening agents include acid salts of metals, cements, hydraulic substances such as plaster, oxides and hydroxides of divalent or higher metals. However, conventional curing agents have a sensitive curing reaction with water-soluble alkali silicate salts, and changes in the amount added immediately affect the reaction rate.
In order to improve the durability, it is necessary to increase the amount of curing agent, which increases the curing speed, shortens the shelf life of the composition, and makes work difficult. was there. Another drawback is that as the reaction rate increases, shrinkage strain within the foam increases, resulting in cracks. The present invention is characterized by using a completely new mineral powder and/or red mud as a hardening component in place of a conventional hardening agent, and the hardening component is hardened with a water-soluble alkali silicate. The present inventors discovered for the first time that although it has a function, its reaction rate is slow, and the reaction rate is not sensitively affected by changes in the amount of compounding.
又、これらの硬化性成分は天然資源として又は産業活動
における副産物として大量にかつ安価に入手できるとい
うところから産業上十分に使用し得るものである。係る
新しい硬化性成分を配合することによって本発明は完成
されたものであり即ち本発明は風水可溶性アルカリ桂酸
塩を主成分とし、【B}金属系発泡剤、硬化性成分とし
て(C}アロフエン、カイアナイト、シリマナイト、ジ
ブサイト、ダイアスポ及びべーマィトから選ばれる少く
とも一種の鉱物の粉体及び/又は赤泥を原料物質としこ
れに{D}水を加えて用いることを特徴とする発泡性を
有する無機質組成物に係るものである。本発明において
A成分としては、可溶性のアルカリ韓酸塩を用いること
を必須とし、これによりはじめて所期の発泡体を収得で
きる。通常の無水水ガラスカレットの如き不溶性ないし
水難溶性のアルカリ金属桂酸塩では、上記発泡体の製造
は不能である。このA成分を構成するアルカリ成分とし
ては、例えばリチウム、ナトリウム、カリウム、ルビジ
ウム等のアルカリ金属及び第4級アンモニウムを例示で
きる。またA成分は水可溶性である限り、その組成やア
ルカリ酸化物(R20として示す)とSiQとのモル比
には本来制限されないのであるが、上記Si02/R2
0のモル比は1.5〜7.0とし、特に1.8〜3.母
屋度とするのが望ましい。上記A成分は、その1種を単
独で又は2種以上を併用して、粉末の形態でも又水溶液
の形態でも有利に用い得るがトペースト調整の容易性を
考慮すれば、固形分濃度を10%以上、通常10〜60
%程度の水溶液の形態で用いるのが好ましい。即ちA成
分を上記範囲の濃度の水溶液の形態で用いる時には、こ
れを他の{Bー〜皿成分及び必要に応じ使用される他の
成分と共に単に混合するだけで容易にペースト状組成物
の調整を行ない得て、適度な流動性が得られると共に硬
化時の収縮率をも比較的少ない。次に本発明においてB
成分とする金属系発泡剤としては、各種の金属元素及び
金属合金ないし金属間化合物が使用できる。金属元素と
しては周期率表OB,mA,mB,WA,NB,VA,
VB,WB,肌B及び血族に属するものがいずれも使用
でき、そのうち第3〜5周期に属するものが好ましく、
かかる金属元素を例示すればCa,Ba,cr,Mn,
Fe,Co,Ni,Cu,Zn,AI,Ga,Si,S
n等が挙げられる。本発明ではまた上記金属の合金ない
し金属間化合物(金属相互間もしくは金属と非金属との
化学結合体)も上記金属と同様に使用でき、談合金ない
し金属間化合物の代表的なものを例示すれば、N−Si
,N−Ti,AI−Mn,AI−Cu−Si,N−Cu
,Zn−S,Zn−Sn,Cu−Si,Fe−Si,S
i−Ni,Co−Sは等が挙げられる。上記B成分は、
通常その1種又は2種以上を約150一以下の粉体で用
いるのが好ましい。本発明に用いられるC成分である硬
化性成分としては次のものをいう。アロフェンは組成式
nSi02・山203・mH20(n=1〜2)で表わ
されるほとんど非晶質の含水アルミ/桂酸塩、カィアナ
ィトは組成式Si02・AI203で表わされるへキ開
性のアルミノ桂酸塩、シリマナィトは組成式Sj02・
N203で表わされる耐火材用のアルミノ桂酸塩、ジプ
サィトは組成式AI(OH)3で表わされ又べーマィト
及びダイアスポは組成式AI○(OH)で表わされるボ
ーキサイトやラテライトなど中に含まれるアルミニウム
の含水酸化物である。又、赤泥は、アルミニウム製練時
に副産物として得られるもので、A!203以外にFe
203及びSi02等を多量に含有しているものである
。これらは有効成分としてかなりの釘203を含んでい
るものであるが、化学的に得られるAI203やAI(
OH)2などとは異なり推定による所では不純成物が何
らかの形で本発明発泡作用及び硬化作用に良好な影響を
するものと思われる。これら硬化性成分はいずれも粉末
状で用いられるものであり、実際の使用に際してはその
ままもしくは予め仮糠した後に本発明の必須原料として
供され、粒度により反応速度は若干変化し粉体粒子が微
細な程反応速度は徐々ながら大きくなる。本発明組成物
の配合割合は、これら各成分とする物質の種類により一
定しないが、通常A成分固形分を基準にして、その10
の重量部に対しB成分は約3〜50重量部とし、C成分
は約20〜50の重量部とする。In addition, these curable components can be sufficiently used industrially because they can be obtained in large quantities and at low cost as natural resources or as by-products of industrial activities. The present invention was completed by blending such a new curable component. That is, the present invention has a feng shui soluble alkali silicate as a main component, [B] a metal foaming agent, and (C) allofene as a curable component. , kyanite, sillimanite, gibbsite, diaspo and boehmite, and/or red mud is used as a raw material, and {D} water is added to the powder, and the foaming property is used. This relates to an inorganic composition. In the present invention, it is essential to use a soluble alkali kolate as the A component, and only then can the desired foam be obtained. It is impossible to manufacture the above-mentioned foam with insoluble or slightly water-soluble alkali metal citrate. Examples of the alkali component constituting component A include alkali metals such as lithium, sodium, potassium, and rubidium, and quaternary ammonium. In addition, as long as component A is water-soluble, there are no restrictions on its composition or the molar ratio of the alkali oxide (shown as R20) and SiQ, but the above Si02/R2
The molar ratio of 0 is set to 1.5 to 7.0, particularly 1.8 to 3.0. It is desirable to use the main building level. The above component A can be advantageously used alone or in combination of two or more in the form of a powder or an aqueous solution, but considering the ease of preparing the paste, the solid concentration should be reduced to 10%. Above, usually 10-60
% in the form of an aqueous solution. That is, when component A is used in the form of an aqueous solution with a concentration within the above range, a paste-like composition can be easily prepared by simply mixing it with other ingredients (B) and other ingredients used as necessary. As a result, appropriate fluidity can be obtained, and the shrinkage rate during curing is also relatively small. Next, in the present invention, B
Various metal elements, metal alloys, and intermetallic compounds can be used as the metallic foaming agent. Metal elements include periodic table OB, mA, mB, WA, NB, VA,
Any of those belonging to VB, WB, skin B, and blood relatives can be used, and among them, those belonging to the 3rd to 5th period are preferable.
Examples of such metal elements include Ca, Ba, cr, Mn,
Fe, Co, Ni, Cu, Zn, AI, Ga, Si, S
Examples include n. In the present invention, alloys or intermetallic compounds (chemical combinations between metals or between metals and non-metals) of the above metals can also be used in the same way as the above metals. If, N-Si
, N-Ti, AI-Mn, AI-Cu-Si, N-Cu
, Zn-S, Zn-Sn, Cu-Si, Fe-Si, S
Examples of i-Ni and Co-S include. The above B component is
It is usually preferable to use one or more of them in powder form of about 150 parts or less. The curable component, which is component C, used in the present invention is as follows. Allophane is a nearly amorphous hydrated aluminum/citrate represented by the composition formula nSi02・yama203・mH20 (n=1-2), and kyanite is a cleavable aluminocinate represented by the composition formula Si02・AI203. Salt, sillimanite has the composition formula Sj02.
Gypsite, an aluminosilicate for refractory materials represented by N203, is represented by the compositional formula AI(OH)3, and boehmite and diaspo are contained in bauxite, laterite, etc., represented by the compositional formula AI○(OH). It is a hydrous oxide of aluminum. Also, red mud is obtained as a by-product during aluminum smelting, and A! Fe other than 203
It contains a large amount of 203, Si02, etc. These contain a considerable amount of nail 203 as an active ingredient, but chemically obtained AI203 and AI (
Unlike OH)2, etc., it is presumed that impurities have a favorable influence on the foaming action and curing action of the present invention in some way. All of these curable components are used in powder form, and when actually used, they are used as essential raw materials for the present invention either as they are or after being branned in advance.The reaction rate varies slightly depending on the particle size, and the powder particles are fine. The reaction rate increases gradually. The blending ratio of the composition of the present invention varies depending on the types of substances used as each of these components, but is usually 10% of the solid content of component A.
Component B is about 3 to 50 parts by weight, and component C is about 20 to 50 parts by weight.
B成分の配合比が少ないと発泡が不充分となり、又多過
ぎると発泡体中の気泡が大きくなって強度が低くなる。
C成分が少ないと硬化反応が進行し難く、又多過ぎると
発泡が困難になる。また、本発明組成物は必要に応じて
着色用顔料、増量材としての無機質不活性粉体あるいは
繊維状物質、軽量骨材等を加えることもでき、このよう
なものとして桂石粉、タルク、カオリン、マイ力、ベン
トナイト、アルミナ、ゼオライト、シリカゲル、活性炭
、カーボンブラック、亜鉛華、石綿、岩綿、パーラィト
、発泡ヒル石、プラスチック発泡体粒子又は粉砕粒子等
が例示できる。本発明における無機質組成物は常温で発
泡するものであるが工場において成形板等の成形体を得
ようとする場合には発泡硬化速度を大きくし生産効率を
上げるために加溢することができる。混合ペーストは所
定の形状の型に流し込み反応せしめるわけであるが、そ
の際に型に入った組成物の混合ペーストを3000から
7000、望ましくは40つ○から6000の間の温度
下に加溢することによって反応を短時間に行わしめ所定
の成形発泡体を得ることができる。この際に加温による
水分の蒸発を急激にさせないために水溶性高沸点溶剤、
例えばエチレングリコール、グリセリン等を加えること
もできる。本発明は上述しているように、極めて容易な
操作で発泡体を得ることができ、係る物質を用いて、軽
量成形板を得るのみならず建物の床に流しこんで断熱床
を形成したり、又壁面に中空部を設けて注入したり、壁
面や天井面の表面に左官塗り又は直接エアーやヱアレス
の吹付方法によりペースト化したものを圧送するあるし
、は吹付ノズル先端で強制混合するなどして塗着せしめ
ることができる他、押出成形機などを用いて発泡成形す
ることもでき、その用途は特に定まるところかない。か
くして得られる発泡体は組成が無機質であるため耐火、
耐熱性にすぐれており、特に従来からの水可溶性アルカ
リ建酸塩からの発泡体に比して圧縮強度が大きく、しか
も硬化時の収縮ひずみが極めて小さいため、発泡硬化体
にほとんどクラツクを生じなく常に価値がある他、浸水
後の圧縮強度の低下もすきぶる小さい。実施例を以下説
明するに当り、試験方法を列挙する。If the blending ratio of component B is too low, foaming will be insufficient, and if it is too high, the bubbles in the foam will become large and the strength will decrease.
If the amount of C component is too small, the curing reaction will be difficult to proceed, and if it is too large, foaming will be difficult. Furthermore, the composition of the present invention may contain coloring pigments, inorganic inert powders or fibrous substances as fillers, lightweight aggregates, etc., as required. Examples of the materials include , miryoku, bentonite, alumina, zeolite, silica gel, activated carbon, carbon black, zinc white, asbestos, rock wool, perlite, foamed vermiculite, plastic foam particles, and pulverized particles. The inorganic composition of the present invention foams at room temperature, but when it is intended to produce molded products such as molded plates in a factory, it can be overflowed to increase the foam curing speed and increase production efficiency. The mixed paste is poured into a mold of a predetermined shape and allowed to react. At this time, the mixed paste of the composition in the mold is flooded at a temperature of 3000 to 7000, preferably 40 to 6000. By doing so, the reaction can be carried out in a short time and a predetermined molded foam can be obtained. At this time, in order to prevent rapid evaporation of water due to heating, a water-soluble high boiling point solvent,
For example, ethylene glycol, glycerin, etc. can also be added. As described above, the present invention allows a foam to be obtained with an extremely easy operation, and by using such a material, not only can a lightweight molded board be obtained, but also it can be poured into the floor of a building to form an insulating floor. Alternatively, the paste may be injected into a hollow part of the wall, plastered on the surface of the wall or ceiling, or a paste made by direct air or Ares spraying may be pumped, or it may be forcefully mixed at the tip of a spray nozzle. In addition to being able to be coated and fixed, it can also be foam-molded using an extrusion molding machine, etc., and its uses are not particularly determined. The foam thus obtained has an inorganic composition, so it is fireproof and
It has excellent heat resistance, and has particularly high compressive strength compared to conventional foams made from water-soluble alkali phosphate salts.Furthermore, the shrinkage strain during curing is extremely small, so there is almost no cracking in the cured foam. Not only is it always valuable, but the loss of compressive strength after immersion in water is also extremely small. In describing the examples below, test methods will be listed.
「試験方法」
ィ 可便時間・・…・粘度が急激に高くならす組成物が
発泡を開始する又は粘度が急激に高くなるまでの時間。"Test method" - Convenience time: The time until the composition whose viscosity increases rapidly starts foaming or the viscosity increases rapidly.
ロ 圧縮強度・・・・・・100柳×100肌×50肋
の成形板を作成したもので圧縮試験する。ハ 耐水性・
・・・・・・・・ロと同じ試験片を水中に9母音間浸潰
した後の表面の変化。B. Compressive strength: A compression test is conducted using a molded plate of 100 willow x 100 skin x 50 ribs. C Water resistance/
・・・・・・・・・Changes in the surface after immersing the same test piece in water for 9 vowels.
異状がなければ−、異状があれば十とする。ニ 収縮ひ
ずみ・・・・・・成形板で発泡硬化せしめた時** の
発泡体の収縮率を%で示し、石綿スレートの面にへラで
3肋厚に塗り、発泡硬化後のクラック発生がない時を−
、クラックが発生する時は十で表示する。If there is no abnormality, score -, if there is any abnormality, score 10. D. Shrinkage strain...The shrinkage rate of the foam is shown in % when it is foamed and cured with a molded plate. It is applied to the asbestos slate surface with a spatula to a thickness of 3 ribs, and cracks occur after the foam is cured. When there is no -
, when a crack occurs, it is displayed as a 10.
ホ 比重・…・・かさ比重
へ 浸水強度・・・・・・ハで試験したた後に圧縮試験
する。E. Specific gravity: Bulk specific gravity Water immersion strength: Perform compression test after testing in C.
実施例 1
市販1号桂酸ソーダ(濃度40重量%)875g、水1
25g、金属アルミニウム粉末50g、ベーマィト粉体
60雌並びにカオリンクレー200gから成る混合物を
鷹梓器を用いて約3分間蝿拝してペーストを得たが、こ
の組成物及び発泡硬化した後の発泡体の性能は第1表に
示すとおりであった。Example 1 Commercially available No. 1 sodium citrate (concentration 40% by weight) 875 g, water 1
A paste was obtained by stirring a mixture of 25g of aluminum powder, 50g of metal aluminum powder, 60g of boehmite powder, and 200g of kaolin clay using a hawker for about 3 minutes. The performance was as shown in Table 1.
又この組成物2ぴ音量を用いて約20〆分吹付塗装した
ところ、15分間で作業をし終え、この間に作業を阻害
する要因は何らなかつた。実施例 2
実施例1において、ベーマィト粉体に変えてカィアナィ
トの600003時間仮暁粉体を用いた他は実施例1と
全く同様にして第1表に示す性能を得た。When this composition was spray coated for about 20 minutes using a volume of 2, the work was completed in 15 minutes, and there were no factors that hindered the work during this time. Example 2 The performance shown in Table 1 was obtained in exactly the same manner as in Example 1, except that kyanite 600,003-hour suspended powder was used instead of boehmite powder.
実施例3及び4
実施例1においてべーマィト粉体に変えて赤泥の粉体の
配合量をそれぞれ100g(実施例3)及び900g(
実施例4)に変えた以外は実施例1と全く同様にして第
1表に示す結果を得た。Examples 3 and 4 In Example 1, the amount of red mud powder was changed to 100 g (Example 3) and 900 g (
The results shown in Table 1 were obtained in exactly the same manner as in Example 1 except that Example 4) was used.
比較例
実施例1においてべ−マィト粉体600gに変えて硫酸
アルミニウム30雌を用いた他は実施例1と全く同様に
試験したところ第1表に示す結果を得た。Comparative Example Tests were conducted in exactly the same manner as in Example 1, except that 30 g of aluminum sulfate was used in place of 600 g of boehmite powder, and the results shown in Table 1 were obtained.
第 1 表Table 1
Claims (1)
ブサイト、ダイアスポ及びベーマイトから選ばれる少く
とも一種の鉱物の粉体及び/又は赤泥、及び(D) 水 を有効成分として含有して成る発泡性を有する無機質組
成物。[Scope of Claims] 1 (A) water-soluble alkali silicate, (B) metallic foaming agent, (C) at least one mineral powder selected from allofene, kyanite, sillimanite, gibbsite, diaspo, and boehmite. and/or red mud, and (D) an inorganic composition having foaming properties that contains water as an active ingredient.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15245180A JPS6025394B2 (en) | 1980-10-28 | 1980-10-28 | inorganic composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15245180A JPS6025394B2 (en) | 1980-10-28 | 1980-10-28 | inorganic composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5777063A JPS5777063A (en) | 1982-05-14 |
| JPS6025394B2 true JPS6025394B2 (en) | 1985-06-18 |
Family
ID=15540801
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP15245180A Expired JPS6025394B2 (en) | 1980-10-28 | 1980-10-28 | inorganic composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6025394B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5845954A (en) * | 1996-06-25 | 1998-12-08 | Toyota Technical Center, U.S.A., Inc. | Glove box assembly including glove box that is positionable in a partially open position |
-
1980
- 1980-10-28 JP JP15245180A patent/JPS6025394B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5777063A (en) | 1982-05-14 |
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