JPH0566908B2 - - Google Patents
Info
- Publication number
- JPH0566908B2 JPH0566908B2 JP61032123A JP3212386A JPH0566908B2 JP H0566908 B2 JPH0566908 B2 JP H0566908B2 JP 61032123 A JP61032123 A JP 61032123A JP 3212386 A JP3212386 A JP 3212386A JP H0566908 B2 JPH0566908 B2 JP H0566908B2
- Authority
- JP
- Japan
- Prior art keywords
- raw materials
- weight
- alc
- content
- silica
- 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
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 32
- 239000002994 raw material Substances 0.000 claims description 18
- 239000000377 silicon dioxide Substances 0.000 claims description 15
- 239000004575 stone Substances 0.000 claims description 10
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 239000012535 impurity Substances 0.000 claims description 4
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 claims description 4
- 235000012239 silicon dioxide Nutrition 0.000 claims description 4
- 235000008733 Citrus aurantifolia Nutrition 0.000 claims description 3
- 235000011941 Tilia x europaea Nutrition 0.000 claims description 3
- 239000004571 lime Substances 0.000 claims description 3
- 239000004568 cement Substances 0.000 claims description 2
- 239000004576 sand Substances 0.000 claims description 2
- 230000001413 cellular effect Effects 0.000 claims 1
- MKTRXTLKNXLULX-UHFFFAOYSA-P pentacalcium;dioxido(oxo)silane;hydron;tetrahydrate Chemical compound [H+].[H+].O.O.O.O.[Ca+2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[O-][Si]([O-])=O.[O-][Si]([O-])=O.[O-][Si]([O-])=O.[O-][Si]([O-])=O.[O-][Si]([O-])=O.[O-][Si]([O-])=O MKTRXTLKNXLULX-UHFFFAOYSA-P 0.000 description 8
- 238000000034 method Methods 0.000 description 6
- 230000000704 physical effect Effects 0.000 description 6
- 238000002441 X-ray diffraction Methods 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 150000004677 hydrates Chemical class 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 239000005995 Aluminium silicate Substances 0.000 description 2
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 2
- 229940037003 alum Drugs 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005187 foaming Methods 0.000 description 2
- 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 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000011398 Portland cement Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- 235000012255 calcium oxide Nutrition 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 238000011088 calibration curve Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000011381 foam concrete Substances 0.000 description 1
- 238000001027 hydrothermal synthesis Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000036314 physical performance Effects 0.000 description 1
- 238000003908 quality control method Methods 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
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
- C04B28/18—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 mixtures of the silica-lime type
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)
- Porous Artificial Stone Or Porous Ceramic Products (AREA)
Description
〔産業上の利用分野〕
本発明は、水蒸気養生軽量気泡コンクリート
(以下ALCと略す)製造方法の改良に関するもの
である。
〔従来の技術〕
ALCは、石灰及びセメント等の石灰質原粉末
とケイ砂、ケイ石等のケイ酸質原料粉末とに水と
アルミニウム粉末などの添加剤を加えてスラリー
状としたのち発泡、半可塑化させ、次いでオート
クレーブに移して高温高圧水蒸気養生を行なつて
製造されている。
このようにして製造されるALCは、ケイ石等
の天然原料を多量に使用するため建築材料として
必要な物理的性能及び耐久性などを保証、向上さ
せるために原料の品位管理に留意する必要があ
る。
ALCを製造するにあたつて最も重要なことは、
製品中に結晶度の高いトバモライトを多量且つ均
質に生成させることである。
このため通常、原料の全石灰分とケイ酸分との
重量比率(以下C/S比と略す)は0.45〜0.80に
なるように管理されている。C/S比が上記の範
囲外では、何れも製品の一部に結晶度の低い水和
物が生成し、結晶度の高いトバモライトの生成を
阻害し、そのため製品の圧縮強度が低下し耐久性
も弱くなる。
また、原料中に含まれるアルカリ成分、アルミ
ナ成分などの不純物も、その含有量によつては、
C/S比が0.45又はそれ以上でも低結晶性の水和
物を生成せしめ、結果的にトバモライトの生成を
妨害し、製品の物性、耐久性を低下させる原因と
なるために、原料の品位管理は厳密に為されてい
る。
前述の低結晶性の水和物の生成を抑える方法と
して、近年、鉱物性のアムミナ物質、例えばカオ
リン、高炉水砕スラグ等を原料の全固形物に対し
て内割りで2〜4重量%程度添加することが行な
われている。このカオリン等の添加によれば一応
圧縮強度等は向上するが、発泡段階で気泡の乱れ
が起こり、それに起因するためか製品の吸水率が
高くなるという欠点があり、コスト高にもなると
いう問題点がある。
また原料については、ケイ酸質原料中のアルカ
リ分が1重量%以下、好ましくは0.0重量%以下
のものを使用すると上述の欠点を緩和するという
知見も得られているが、主要原料の管理のみに関
しては今だに充分な成果は得られていないのが現
状である。
〔発明が解決しようとする問題点〕
本発明の目的は、上記の欠点がなく且つ原料の
配合比、C/S比を0.40程度まで下げても安定し
て望ましい物性を示すALCを製造しうる方法を
提供することにある。
〔問題点を解決するための手段〕
この目的を達成するため、本願発明者は鋭意研
究の結果、ALCの主要原料であるケイ石を、該
ケイ石中の不純物として含有される明礬石含有率
を1.6重量%以下のものに限定して使用し、以下
通常の方法に従つてALCを製造するというもの
である。
〔作用〕
本発明の方法において、主要原料のケイ石を、
該ケイ石中の不純物として含有される明礬石
(K2O・3Al2O3・4SO3・6H2O)の含有率を1.6重
量%以下のものに限定して使用する理由は、明礬
石含有率が1.6重量%以上のものを使用すると、
水熱反応の過程でこれが微妙な影響を及ぼし、
C/S比を例えば0.6〜0.8と高めとした場合でも
高結晶性のトバモライトが得られず、ALCの物
性特に圧縮強度が大幅に悪化する現象の実験的知
見に基づいて決めたものである。
ケイ石中の明礬石含有率は、生産地にもよるが
通常1.0〜3.0重量%の範囲に分析しており、この
明礬石の占めるケイ石中の割合がどうして特にオ
ートクレーブ養生過程で均質な水熱合成を阻害
し、高結晶性のトバモライトの生成が妨げられる
のか、その理由については明確ではないが、例え
ばALC製造の過程で生成するケイ酸カルシウム
水和物から結晶性のトバモライトへの移行時に、
該明礬石が分解し、そして溶解した同イオンが微
妙に影響してトバモライトの生成を妨害するので
はないかと想像される。
本発明法によれば、C/S比0.4以上の配合で
特に余分な添加剤を添加することなしに充分な物
性のALCを確実に得ることができる。
〔実施例〕
以下実施例について説明する。
実施例
明礬石含有率が0.1〜2.8重量%のケイ石と生石
灰及びポルトランドセメントの主要原料をC/S
比が所定値となるように配合し、これに硫酸カル
シウムの所定量と水と少量のアルミニウム粉末
(0.063重量部)及び通常の添加剤を添加し以下常
法に従つてALCを製造し、その圧縮強度は、JIS
A−5416−7項により、トバモライトの同定はタ
ーゲツトCuのX線回折により夫々測定した。そ
の結果を第1表及び第2表に比較例と対比して示
す。
[Industrial Application Field] The present invention relates to an improvement in a method for producing steam-cured lightweight cellular concrete (hereinafter abbreviated as ALC). [Prior technology] ALC is a slurry made by adding water and additives such as aluminum powder to calcareous raw powder such as lime and cement and silicic acid raw powder such as silica sand and silica stone, and then foaming and semi-slurry. It is manufactured by plasticizing it, then transferring it to an autoclave and curing it with high temperature and high pressure steam. ALC manufactured in this way uses a large amount of natural raw materials such as silica stone, so care must be taken to control the quality of the raw materials in order to guarantee and improve the physical performance and durability required as a building material. be. The most important thing when manufacturing ALC is
The objective is to uniformly produce a large amount of highly crystalline tobermorite in the product. For this reason, the weight ratio of the total lime content to silicic acid content (hereinafter abbreviated as C/S ratio) of the raw material is usually controlled to be 0.45 to 0.80. If the C/S ratio is outside the above range, hydrates with low crystallinity will form in some parts of the product, inhibiting the formation of tobermorite with high crystallinity, and therefore the compressive strength of the product will decrease and durability will deteriorate. It also becomes weaker. In addition, impurities such as alkali components and alumina components contained in raw materials may also be affected depending on their content.
Even if the C/S ratio is 0.45 or higher, low-crystalline hydrates will be produced, which will eventually interfere with the production of tobermorite and reduce the physical properties and durability of the product, so quality control of raw materials is required. is strictly followed. As a method of suppressing the formation of the aforementioned low-crystalline hydrates, in recent years mineral amimina substances such as kaolin, granulated blast furnace slag, etc. have been used in an amount of about 2 to 4% by weight based on the total solid content of the raw materials. It is being added. Although the addition of kaolin and the like improves the compressive strength to a certain extent, it has the disadvantage that the bubbles become disordered during the foaming stage, which increases the water absorption rate of the product, which also increases the cost. There is a point. Regarding raw materials, it has been found that using silicic acid raw materials with an alkaline content of 1% by weight or less, preferably 0.0% by weight or less, alleviates the above-mentioned drawbacks, but it is only possible to control the main raw materials. Currently, sufficient results have not been obtained in this regard. [Problems to be Solved by the Invention] The purpose of the present invention is to produce an ALC that does not have the above-mentioned drawbacks and stably exhibits desirable physical properties even when the blending ratio of raw materials and C/S ratio is lowered to about 0.40. The purpose is to provide a method. [Means for Solving the Problems] In order to achieve this objective, the inventor of the present application has conducted extensive research and found that the content of silica stone, which is the main raw material of ALC, has been improved by reducing the content of alumite contained as an impurity in the silica stone. ALC is produced by using a limited amount of 1.6% by weight or less, and following a conventional method. [Operation] In the method of the present invention, the main raw material, silica stone, is
The reason why the content of alumite (K 2 O・3Al 2 O 3・4SO 3・6H 2 O) contained as an impurity in the silica stone is limited to 1.6% by weight or less is that If you use a substance with a content of 1.6% by weight or more,
This has a subtle effect on the hydrothermal reaction process,
This was determined based on the experimental findings that even when the C/S ratio is set to a high value of 0.6 to 0.8, highly crystalline tobermorite cannot be obtained, and the physical properties of ALC, particularly the compressive strength, are significantly deteriorated. The alumite content in silica stone is usually analyzed to be in the range of 1.0 to 3.0% by weight, depending on the place of production. It is not clear why thermal synthesis is inhibited and the production of highly crystalline tobermorite is prevented, but for example, during the transition from calcium silicate hydrate produced in the ALC manufacturing process to crystalline tobermorite. ,
It is thought that the alumite decomposes and the dissolved ions subtly influence the formation of tobermorite. According to the method of the present invention, it is possible to reliably obtain ALC with sufficient physical properties without adding any extra additives when the C/S ratio is 0.4 or more. [Example] Examples will be described below. Example C/S silica with an alumite content of 0.1 to 2.8% by weight, quicklime, and the main raw materials for Portland cement
ALC is produced by adding a predetermined amount of calcium sulfate, water, a small amount of aluminum powder (0.063 parts by weight), and usual additives to the mixture so that the ratio becomes a predetermined value. Compressive strength is JIS
According to Section A-5416-7, tobermorite was identified by X-ray diffraction of target Cu. The results are shown in Tables 1 and 2 in comparison with comparative examples.
【表】
表註※ケイ石中の明礬石の含有率の定量は、ケ
イ石に純粋な明礬石の各所定量を添加し、X線回
折によるメインピーク(2θ=30℃)の強度により
検量線を作成し、同様の操作で各試料をX線回折
にかけ、これを換算して品位に測定した。
第1表より明らからなように、原料の配合比を
同じにしてケイ石の明礬石の含有率のみ変動させ
たところ、同品位が1.8重量%遺贈のものは圧縮
強度がその期待値40.0Kgf/cm2より大幅に低下し
たが、それ以外は充分な圧縮強度が得られX線回
折の結果も満足するに足るものであつた。[Table] Table note *To quantify the content of alum in silica, add each predetermined amount of pure alum to silica, and use the intensity of the main peak (2θ = 30℃) by X-ray diffraction to calculate the calibration curve. Each sample was subjected to X-ray diffraction using the same procedure, and this was converted to determine the quality. As is clear from Table 1, when the blending ratio of raw materials was kept the same and only the alumite content of silica stone was varied, the compressive strength of the bequest with the same grade of 1.8% by weight was the expected value of 40.0Kgf. /cm 2 , but other than that, sufficient compressive strength was obtained and the results of X-ray diffraction were also satisfactory.
本発明によれば、特に物性改善のための添加剤
を入れなくても又C/S比を厳密に管理しなくて
も、良好な物性を備えたALCを製造することが
できる。
According to the present invention, ALC with good physical properties can be produced without adding any additives for improving physical properties or without strictly controlling the C/S ratio.
Claims (1)
イ石等のケイ酸質原料とを主要原料とする水蒸気
養生軽量気泡コクリートの製造法において、上記
ケイ石中に不純物として明礬石を1.6重量%以下
含有するケイ酸質原料を使用することを特徴とす
るALCB製造方法。1. In a method for producing steam-cured lightweight cellular cocrete whose main raw materials are calcareous raw materials such as lime and cement and silicic raw materials such as silica sand and silica stone, 1.6% by weight or less of alumite is contained as an impurity in the silica stone. An ALCB manufacturing method characterized by using a silicic acid raw material containing.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3212386A JPS62191481A (en) | 1986-02-17 | 1986-02-17 | Manufacture of alc |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3212386A JPS62191481A (en) | 1986-02-17 | 1986-02-17 | Manufacture of alc |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62191481A JPS62191481A (en) | 1987-08-21 |
JPH0566908B2 true JPH0566908B2 (en) | 1993-09-22 |
Family
ID=12350105
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3212386A Granted JPS62191481A (en) | 1986-02-17 | 1986-02-17 | Manufacture of alc |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62191481A (en) |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS567994A (en) * | 1979-06-29 | 1981-01-27 | Matsushita Electric Works Ltd | Floor panel for floor heating |
-
1986
- 1986-02-17 JP JP3212386A patent/JPS62191481A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS567994A (en) * | 1979-06-29 | 1981-01-27 | Matsushita Electric Works Ltd | Floor panel for floor heating |
Also Published As
Publication number | Publication date |
---|---|
JPS62191481A (en) | 1987-08-21 |
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