JPH01246122A - Spherical particle of xonotlite for molding material and production thereof - Google Patents

Spherical particle of xonotlite for molding material and production thereof

Info

Publication number
JPH01246122A
JPH01246122A JP7319588A JP7319588A JPH01246122A JP H01246122 A JPH01246122 A JP H01246122A JP 7319588 A JP7319588 A JP 7319588A JP 7319588 A JP7319588 A JP 7319588A JP H01246122 A JPH01246122 A JP H01246122A
Authority
JP
Japan
Prior art keywords
xonotlite
specific gravity
weight
silica powder
slaked lime
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.)
Granted
Application number
JP7319588A
Other languages
Japanese (ja)
Other versions
JPH0822735B2 (en
Inventor
Hideo Uchiyama
秀男 内山
Toshihiro Nakada
中田 敏宏
Mariko Kawamura
河村 真理子
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.)
Ube Corp
Original Assignee
Ube Industries 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 Ube Industries Ltd filed Critical Ube Industries Ltd
Priority to JP7319588A priority Critical patent/JPH0822735B2/en
Publication of JPH01246122A publication Critical patent/JPH01246122A/en
Publication of JPH0822735B2 publication Critical patent/JPH0822735B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Porous Artificial Stone Or Porous Ceramic Products (AREA)
  • Silicates, Zeolites, And Molecular Sieves (AREA)

Abstract

PURPOSE:To obtain the subject material having small apparent specific gravity and improved strength and formability by the hydrothermal synthetic reaction of a specific slaked lime and silica powder in the presence of water. CONSTITUTION:Slaked lime having an Al2O3 content of <=0.1wt.% is mixed with silica powder having an Al2O3 content of 0.5-3wt.% at an SiO2/CaO molar ratio of 1.00. The obtained raw material is added with 5-15 times weight of water and subjected to hydrothermal synthetic reaction in an autoclave under stirring to obtain spherical particle of xonotlite having an apparent specific gravity of 0.15-0.17 and a double-layer structure composed of an inner core and an outer shell connected with each other in the form of a network through acicular xonotlite crystals. 100pts.wt. of a slurry containing said particle is mixed with 1-20pts.wt. of an emulsion of a polymer such as styrene-butadiene copolymer, 1-10pts.wt. of a reinforcing fiber and, as necessary, dispersing agent, expansion material, etc., the mixture is filled in a mold and compression molded and the product is dried at 100-180 deg.C to obtain a xonotlite molded article having a bulk specific gravity of 0.3-0.7.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は、嵩比重が0.3〜0.8の建築材料用成形材
料として好適なゾノトライト球状粒子およびその製造方
法に関するものでおる。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to zonotrite spherical particles having a bulk specific gravity of 0.3 to 0.8 and suitable as a molding material for building materials, and a method for producing the same.

[従来の技術] 水存在下で攪拌しながら水熱合成反応したケイ酸カルシ
ウム(′通常はトバモライト必るいはゾノトライト)は
軽量で熱的に安定な物質でおり、この特性を利用した高
比重が0.3以下のケイ酸カルジム成形体は断熱材、保
温材として広く使用されている。
[Prior art] Calcium silicate (usually tobermorite or xonotlite) produced by hydrothermal synthesis reaction while stirring in the presence of water is a lightweight and thermally stable substance, and this property can be used to produce high specific gravity. Caldium silicate molded bodies with a density of 0.3 or less are widely used as heat insulating materials and heat retaining materials.

またケイ酸カルシウムに補強繊維、ラテックス等を添加
し、嵩比重0.3〜0.7に成形して人造木材を製造し
ようとする試みも(1)特開昭60−24625号公報
などに提案されている。
In addition, an attempt to manufacture artificial wood by adding reinforcing fibers, latex, etc. to calcium silicate and molding it to a bulk specific gravity of 0.3 to 0.7 was proposed in (1) JP-A No. 60-24625, etc. has been done.

[発明が解決しようとする課題] ケイ酸カルシウム(通常はゾノトライトあるいはトバモ
ライト)は水熱合成反応によってつくられ、成形体はこ
のケイ酸カルシウムを成形後、乾燥して製造される。従
来提案されているケイ酸カルシウム球状粒子は殻が薄く
、嵩比重0.3〜0.7の成形体製造用として使用した
場合、殻が変形したり、破壊してその球状粒子が有する
特性がそこなわれる。ざらにはその変形や破壊のために
成形性能が低下する、すなわち成形時の水ぬ(プが悪く
なる傾向がある。
[Problems to be Solved by the Invention] Calcium silicate (usually xonotrite or tobermorite) is produced by a hydrothermal synthesis reaction, and a molded article is produced by molding this calcium silicate and then drying it. The previously proposed calcium silicate spherical particles have thin shells, and when used to produce molded products with a bulk specific gravity of 0.3 to 0.7, the shells may deform or break, causing the properties of the spherical particles to deteriorate. It will be damaged. Moreover, molding performance tends to deteriorate due to deformation and destruction, that is, water retention during molding tends to deteriorate.

[課題を解決するための手段] 本発明は2重の殻構造を有し、その内殻と外殻がゾノト
ライト針状結晶により、網目状につながっているゾノト
ライト球状粒子およびその製造方法に関するものでおる
[Means for Solving the Problems] The present invention relates to spherical zonotolite particles having a double shell structure, the inner shell and the outer shell of which are connected in a network shape by needle-like xonotrite crystals, and a method for producing the same. is.

本発明のゾノトライト球状粒子は、酸化アルミニウム成
分量(以下、単にアルミニウム量と略す。)0.1重量
パーセント以下の消石灰とアルミナ量が0.5重量パー
セント以上3重旧パーセント以下のケイ石粉を水の存在
下で攪拌しながらオートクレーブ中で水熱合成反応させ
て得られる。
The zonotolite spherical particles of the present invention are made by mixing slaked lime with an aluminum oxide content (hereinafter simply referred to as aluminum content) of 0.1% by weight or less and silica powder with an alumina content of 0.5% by weight or more and 3% by weight or less. It is obtained by carrying out a hydrothermal synthesis reaction in an autoclave while stirring in the presence of.

このようにして得られたゾノトライト球状粒子は、みか
けの比重が0.15〜0.17と軽くても成形した場合
変形や破壊を生じにくく、成形性のよい高強度を有する
ケイ酸カルシウム成形体を製造できる。
The zonotolite spherical particles obtained in this way are hard to deform or break when molded even though their apparent specific gravity is as light as 0.15 to 0.17, and the calcium silicate molded product has good moldability and high strength. can be manufactured.

上記のような原料を使用した場合、2重の殻を有するゾ
ノトライトを生成する理由は明確ではないが、生石灰を
使用したり、アルミナ】が0.5重量パーセント以下の
ケイ石を使用した場合、2重設ではなく薄い殻のゾノト
ライトしか生成しない。また、アルミナ量が3重量パー
セント以上のケイ石粉や、アルミナ成分を別途添加した
場合も反応時間が遅くなるだけで、上記のようなゾノト
ライトは生成しない。
It is not clear why xonotrite with a double shell is produced when the above raw materials are used, but when quicklime is used or silica stone containing 0.5% by weight or less of alumina is used, Only thin-shelled xonotlites are produced instead of double structures. Furthermore, if silica powder containing 3% by weight or more of alumina or an alumina component is separately added, the reaction time will only be delayed and the above-mentioned xonotrite will not be produced.

本発明に使用する消石灰としては市販の低アルミナ含有
のものが使用され、ケイ石粉はアルミナ量を0.5重量
パーセント以上3重量パーセント以下含有するケイ石を
ブレーン比表面積5000〜10000cn/9に粉砕
したものが使用される。
The slaked lime used in the present invention is commercially available with low alumina content, and the silica powder contains 0.5% by weight or more and 3% by weight or less of alumina and is ground to a Blaine specific surface area of 5000 to 10000 cn/9. is used.

また、水とこれら原料との配合割合は水/(消石灰+ケ
イ石粉)重量比で5〜15である。
Moreover, the mixing ratio of water and these raw materials is 5 to 15 in weight ratio of water/(slaked lime + silica powder).

次に本発明のゾノトライト系成形体の好適な製造法の一
例を示す。
Next, an example of a preferred method for producing the xonotlite molded article of the present invention will be described.

S i 02 /CaO(モル比)が1.00になるよ
うに、アルミナ!U)、1重量パーセント以下の消石灰
とアルミナ10.5重fflパーセント以上3重ロバ−
セント以下のケイ石粉を配合し、原料に対して水を5〜
15重量倍加えて水熱合成反応させ、ゾノトライトスラ
リーを得る。水熱合成反応は一般にオートクレーブを使
用して行われる。この合成したゾノトライトスラリーの
固形分100重量部に対して、1〜20重量部のスチレ
ン−ブタジェン共重合体、アクリル酸エステル重合体等
の重合体エマルジョン、1〜10重量部のガラス繊維等
の補強繊維、その他に必要に応じて分散剤、膨張材を添
加混合した後、このスラリーを嵩比重0.3〜0.7に
なるように成形する。成形法としては例えば形枠に充填
して加圧脱水する方法が挙げられるが、目的、用途に応
じて従来公知の成形法が適宜採用される。この成形体を
乾燥すると目的とするゾノトライト系成形体いわゆる人
造木材が得られる。乾燥する際の温度は特に制限されな
いが、100〜180℃通常110〜160’Cの温度
が採用される。
Alumina! so that S i 02 /CaO (molar ratio) is 1.00! U), 1 weight percent or less of slaked lime and alumina 10.5 weight percent or more of triple weight
Contains silica powder of less than cents, and adds 5 to 50% water to the raw materials.
Add 15 times the amount by weight and carry out a hydrothermal synthesis reaction to obtain a xonotrite slurry. Hydrothermal synthesis reactions are generally carried out using autoclaves. Based on 100 parts by weight of the solid content of the synthesized xonotrite slurry, 1 to 20 parts by weight of a polymer emulsion such as a styrene-butadiene copolymer or an acrylic ester polymer, and 1 to 10 parts by weight of reinforcement such as glass fiber, etc. After adding and mixing fibers, a dispersant, and an expansion material as necessary, this slurry is molded to have a bulk specific gravity of 0.3 to 0.7. As a molding method, for example, a method of filling a mold and dehydrating under pressure may be mentioned, but a conventionally known molding method may be appropriately adopted depending on the purpose and use. When this molded product is dried, the desired xonotlite-based molded product, so-called artificial wood, is obtained. The temperature for drying is not particularly limited, but a temperature of 100 to 180°C, usually 110 to 160'C is employed.

以下に本発明の実施例を示すが本発明は実施例に限定さ
れない。なお、いずれも加圧成形する際の圧力を2〜5
段階にかえ、高比重が2〜5段階に相違する成形体を調
製し物性を試験した。
Examples of the present invention are shown below, but the present invention is not limited to the examples. In addition, in both cases, the pressure during pressure molding was set to 2 to 5.
Instead of different stages, molded bodies with different high specific gravity levels from 2 to 5 stages were prepared and their physical properties were tested.

[実施例] 成形体物性試験方法は次によった。[Example] The physical properties of the molded body were tested as follows.

(1)曲げ強度:JIS  A1408に準じた。(1) Bending strength: According to JIS A1408.

(2)比 強 度:(曲げ強度)/(嵩比重−)(3)
成形速度:加圧成形する際にスラリーが金型より吹出ざ
ない最高成形 速度。
(2) Specific strength: (bending strength) / (bulk specific gravity -) (3)
Molding speed: Maximum molding speed at which slurry does not blow out of the mold during pressure molding.

(4)乾燥収縮率ニブレス成形後および乾燥後の成形体
の厚さを測定し、乾燥 時の収縮率を求めた。
(4) Drying shrinkage rate The thickness of the molded product after nibless molding and drying was measured to determine the shrinkage rate during drying.

実施例1 第1表に示すケイ石粉1と消石灰とを5in2 :Ca
Oのモル比が1:1になるように配合し、原料相lに対
して12倍量の水を加えてオートクレーブ中で攪拌しな
がら温度210℃、圧力19f(y/criで3時間水
熱合成反応させた。得られたゾノトライトの電子顕微鏡
写真を第1図および第2図に示す。また得られたゾノト
ライトの物性を第2表に示す。
Example 1 Silica stone powder 1 shown in Table 1 and slaked lime were mixed in 5 in2 :Ca
Blend so that the molar ratio of O is 1:1, add 12 times the amount of water to the raw material phase 1, and hydrothermally heat in an autoclave at a temperature of 210°C and a pressure of 19f (y/cri) for 3 hours with stirring. A synthetic reaction was carried out. Electron micrographs of the obtained xonotlite are shown in Figures 1 and 2. Table 2 shows the physical properties of the obtained xonotlite.

この得られたゾノトライトスラリーに、ゾノトライト結
晶100重量部に対してアクリル酸エステルエマルジョ
゛ン(昭和高分子■製、商品名AT−20)固体重量5
重量部、分散剤(藤沢薬品■製、商品名バリツク#1)
0.5重量部および膨張材(N気化学■、商品名C3A
#20)5重量部を添加、混合した後、ガラス繊維(日
東紡績■、商品名C812GYD)7重量部を添加混合
した。
To the obtained xonotrite slurry, acrylic acid ester emulsion (manufactured by Showa Kobunshi ■, trade name AT-20) solid weight 5 was added to 100 parts by weight of xonotrite crystals.
Parts by weight, dispersant (manufactured by Fujisawa Yakuhin ■, trade name Balik #1)
0.5 parts by weight and expansion material (N gas chemical ■, trade name C3A
After adding and mixing 5 parts by weight of #20), 7 parts by weight of glass fiber (Nitto Boseki ■, trade name C812GYD) was added and mixed.

得られた高分散性ゾノトライトスラリーをプレス成形し
、140℃で16時間乾燥しゾノトライト系成形体を得
た。成形体の試験結果を第3表に示す。
The obtained highly dispersed xonotrite slurry was press-molded and dried at 140°C for 16 hours to obtain a xonotrite-based molded body. The test results of the molded bodies are shown in Table 3.

第3表 単イ立 本L:  kgf/cn+”   本2:  
kgf/cm”  本3:  kgf/cm2−min
*4:% 実施例2 ケイ石原料として第1表に示すケイ石粉2を使用°した
以外は、′実施例1と同様にして得られたゾノトライト
の電子顕微鏡写真を第3図に示す。また、得られたゾノ
トライトの物性を第2表に示す。
Table 3 Single item Book L: kgf/cn+” Book 2:
kgf/cm” Book 3: kgf/cm2-min
*4:% Example 2 Figure 3 shows an electron micrograph of xonotlite obtained in the same manner as in Example 1, except that silica powder 2 shown in Table 1 was used as the silica raw material. Further, the physical properties of the obtained xonotlite are shown in Table 2.

実施例1と同様にして得られた成形体の試験結果を第3
表に示す。
The test results of the molded body obtained in the same manner as in Example 1 were
Shown in the table.

実施例3 ケイ石原料として第1表に示すケイ石粉3を使用した以
外は、実施例1と同様にして得られたゾノトライトの電
子顕微鏡写真を第4図に示す。また、得られたゾノトラ
イトの物性を第2表に示す。
Example 3 FIG. 4 shows an electron micrograph of xonotlite obtained in the same manner as in Example 1, except that silica powder 3 shown in Table 1 was used as the silica raw material. Further, the physical properties of the obtained xonotlite are shown in Table 2.

実施例1と同様にして得られた成形体の試験結果、を第
3表に示す。
Table 3 shows the test results of the molded bodies obtained in the same manner as in Example 1.

2此較例1 ケイ石原料として第1表に示すケイ石粉4を使用した以
外は、実施例1と同様にして得られたゾノトライトの電
子顕微鏡写真を第5図に示す。また、得られたゾノトラ
イトの物性を第2表に示す。
2 Comparative Example 1 FIG. 5 shows an electron micrograph of xonotlite obtained in the same manner as in Example 1, except that silica powder 4 shown in Table 1 was used as the silica raw material. Further, the physical properties of the obtained xonotlite are shown in Table 2.

実施例1と同様にして得られた成形体の試験結果を第4
表に示す。
The test results of the molded body obtained in the same manner as in Example 1 were
Shown in the table.

第4表(1) 単位 d:  kgf/cm”   本2:  kgf
/cm”   本3:  kgf/cm”、min本4
: % 第4表(2) 単イ立 本1:  kgf/cm2 本2:  kgf
/cm2 本3:  kgfz’c+y+″、min本
4: % 比較例2 ケイ石原料として第1表に示すケイ石粉5を使用した以
外は、゛実施例1と同様にして得られたゾノトライトの
電子顕微鏡写真を第6図に示す。また、得られたゾノト
ライトの物性を第2表に示す。
Table 4 (1) Unit d: kgf/cm” Book 2: kgf
/cm” book 3: kgf/cm”, min book 4
: % Table 4 (2) Single unit Book 1: kgf/cm2 Book 2: kgf
/cm2 Book 3: kgfz'c+y+'', min Book 4: % Comparative Example 2 Electrons of xonotlite obtained in the same manner as in Example 1, except that silica powder 5 shown in Table 1 was used as the silica raw material. A micrograph is shown in Fig. 6. The physical properties of the obtained xonotlite are shown in Table 2.

実施例1と同様にして得られた成形体の試験結果を第4
表に示す。
The test results of the molded body obtained in the same manner as in Example 1 were
Shown in the table.

比較例3 ケイ石原料として第1表に示すケイ石粉6を使用した以
外は、実施例1と同様にして得られたゾノトライトの電
子顕微鏡写真を第7図に示す。また、得られたゾノトラ
イトの物性を第2表に示す。
Comparative Example 3 FIG. 7 shows an electron micrograph of xonotlite obtained in the same manner as in Example 1, except that silica powder 6 shown in Table 1 was used as the silica raw material. Further, the physical properties of the obtained xonotlite are shown in Table 2.

実施例1と同様にして得られた成形体の試験結果を第4
表に示す。
The test results of the molded body obtained in the same manner as in Example 1 were
Shown in the table.

比較例4 消石灰の代わりに第1表に示す生石灰を使用した以外は
、実施例1と同様にして得られたゾノトライトの電子顕
微鏡写真を第8図に示す。また、得られたゾノトライト
の物性を第2表に示す。実施例1と同様にして得られた
成形体の試験結果を第4表に示す。
Comparative Example 4 FIG. 8 shows an electron micrograph of xonotlite obtained in the same manner as in Example 1, except that quicklime shown in Table 1 was used instead of slaked lime. Further, the physical properties of the obtained xonotlite are shown in Table 2. Table 4 shows the test results of the molded bodies obtained in the same manner as in Example 1.

[発明の効果] 本発明は、嵩比重が0.3〜0.8の建築材料用成形材
料おるいは人造木材として好適に利用されるゾノトライ
ト球状粒子とその製造方法を提供している。
[Effects of the Invention] The present invention provides zonotrite spherical particles having a bulk specific gravity of 0.3 to 0.8 and suitably used as a molding material for building materials or artificial wood, and a method for producing the same.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図・第2図は、実施例1において得られたゾノトラ
イト球状粒子の結晶構造を表す電子顕微鏡写真(倍率1
000倍・5000倍で必る)。 第3図は、実施例2において得られたゾノトライト球状
粒子の結晶構造を表す電子顕微鏡写真(倍率1000倍
)である。 第4図は、実施例3において得られたゾノトライト球状
粒子の結晶構造を表す電子顕微鏡写真(倍率1000倍
)である。 第5図は、比較例1において得られたゾノトライト球状
粒子の結晶構造を表す電子顕微鏡写真(倍率1000倍
)でおる。 第6図は、比較例2において得られたゾノトライト球状
粒子の結晶構造を表す電子顕微鏡写真(倍率1000倍
)である。 第7図は、比較例3において得られたゾノトライト球状
粒子の結晶構造を表す電子顕微鏡写真(倍率1ooo倍
)でおる。 第8図は、比較例4において得られたゾノトライト球状
粒子の結晶構造を表す電子顕微鏡写真(倍率1000倍
)でおる。 特許出願人   宇部興産株式会社 第 1・図 第2z@ 第3図 第″l−図 第(図 第す図 第7図 第8 図
Figures 1 and 2 are electron micrographs (magnification: 1
000x and 5000x). FIG. 3 is an electron micrograph (1000x magnification) showing the crystal structure of the zonotrite spherical particles obtained in Example 2. FIG. 4 is an electron micrograph (1000x magnification) showing the crystal structure of the zonotrite spherical particles obtained in Example 3. FIG. 5 is an electron micrograph (1000x magnification) showing the crystal structure of the zonotrite spherical particles obtained in Comparative Example 1. FIG. 6 is an electron micrograph (1000x magnification) showing the crystal structure of the zonotrite spherical particles obtained in Comparative Example 2. FIG. 7 is an electron micrograph (100x magnification) showing the crystal structure of the zonotrite spherical particles obtained in Comparative Example 3. FIG. 8 is an electron micrograph (1000x magnification) showing the crystal structure of the zonotrite spherical particles obtained in Comparative Example 4. Patent Applicant: Ube Industries, Ltd. Figure 1, Figure 2z @ Figure 3, ``l-Figure (Figure 7, Figure 8)

Claims (2)

【特許請求の範囲】[Claims] (1)2重の殻構造を有し、その内殻と外殻がゾノトラ
イト針状結晶により、網目状につながっていることを特
徴とするゾノトライト球状粒子。
(1) Zonotlite spherical particles having a double shell structure, the inner and outer shells of which are connected in a network shape by needle-shaped xonotrite crystals.
(2)酸化アルミニウム成分量が0.1重量パーセント
以下の消石灰と酸化アルミニウム成分量が0.5重量パ
ーセント以上3重量パーセント以下のケイ石粉を、水存
在下で攪拌しながら水熱合成反応してなる、2重の殻構
造を有し、その内殻と外殻がゾノトライト針状結晶によ
り、網目状につがっているゾノトライト球状粒子の製造
方法。
(2) Slaked lime with an aluminum oxide content of 0.1% by weight or less and silica powder with an aluminum oxide content of 0.5% by weight or more and 3% by weight or less are subjected to a hydrothermal synthesis reaction while stirring in the presence of water. A method for producing zonotolite spherical particles having a double shell structure, the inner shell and the outer shell of which are connected in a network shape by needle-like xonotrite crystals.
JP7319588A 1988-03-29 1988-03-29 Zonotolite spherical particles for molding material and method for producing the same Expired - Fee Related JPH0822735B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7319588A JPH0822735B2 (en) 1988-03-29 1988-03-29 Zonotolite spherical particles for molding material and method for producing the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7319588A JPH0822735B2 (en) 1988-03-29 1988-03-29 Zonotolite spherical particles for molding material and method for producing the same

Publications (2)

Publication Number Publication Date
JPH01246122A true JPH01246122A (en) 1989-10-02
JPH0822735B2 JPH0822735B2 (en) 1996-03-06

Family

ID=13511118

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7319588A Expired - Fee Related JPH0822735B2 (en) 1988-03-29 1988-03-29 Zonotolite spherical particles for molding material and method for producing the same

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Country Link
JP (1) JPH0822735B2 (en)

Also Published As

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