JPS5921558A - Manufacture of calcium silicate formed body - Google Patents

Manufacture of calcium silicate formed body

Info

Publication number
JPS5921558A
JPS5921558A JP12942582A JP12942582A JPS5921558A JP S5921558 A JPS5921558 A JP S5921558A JP 12942582 A JP12942582 A JP 12942582A JP 12942582 A JP12942582 A JP 12942582A JP S5921558 A JPS5921558 A JP S5921558A
Authority
JP
Japan
Prior art keywords
slurry
raw material
water
lime
calcium silicate
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
JP12942582A
Other languages
Japanese (ja)
Other versions
JPH0158147B2 (en
Inventor
輝 高橋
数雄 柴原
迫田 豊彦
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.)
Ohara Inc
Original Assignee
Ohara Inc
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 Ohara Inc filed Critical Ohara Inc
Priority to JP12942582A priority Critical patent/JPS5921558A/en
Publication of JPS5921558A publication Critical patent/JPS5921558A/en
Publication of JPH0158147B2 publication Critical patent/JPH0158147B2/ja
Granted legal-status Critical Current

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  • Curing Cements, Concrete, And Artificial Stone (AREA)
  • Silicates, Zeolites, And Molecular Sieves (AREA)

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 本発明は珪酸fjルシウム成形体及び子の製法((関“
す。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing an fj lucium silicate molded article and a product.
vinegar.

珪酸力ルシウへ成形体は軽量であること、断熱性に優れ
ていること、耐火性の大きいこと、その他数多くの特徴
を有するがために各種の分野に於いて広く利用されてい
る。また珪酸ハルシウムの結晶の種類とし2ても各種の
ものが広く利用されており、たとえば代表的なものとし
でl−ベル上ライ1−族のものやワラス)〜士イト族の
もの等を例示−J゛ろことが出来る。
Molded silicic acid products are widely used in various fields because they are lightweight, have excellent heat insulation properties, have high fire resistance, and have many other characteristics. In addition, various types of halcium silicate crystals are widely used, and representative examples include those of the L-Bel-Grai 1- group and those of the Walas) to Shiite groups. - I can do a lot of things.

本発明者&J珪酸bルシウム成形体K Qいて従平から
イ!1[究を続けて来たが、この仙弗に於い−C1珪酸
j]ルシウt、成形体の従来公知の製法の−゛−)であ
る15法即ち珪酸原料、石灰原料及び水から調製I〜た
原わスラリー全加用斗加熱攪拌しながら合成反応を行な
わしめて珪酸ハルシラへ結晶の水性ス)リーを得、該珪
酸カルシ「゛ツム結晶の水性スラリーを成形、乾燥する
方法に於い−c1]1皮及びアルニーニー「)乙、化α
物を該F↑酸力ルシウへ結晶の71・・1′[ス−うす
−に添加するときは、得られる成形体の常温乾燥収縮が
著しく低トーすることが判明I7た。またこの研究に於
いて、原料スラリ・−にその固形分に対し。
Inventor & J Lucium silicate molded body K Q and I from Yohei! 1. We have continued to research, and in this study, we have found that -C1 silicate is prepared by the 15 conventional methods for producing molded bodies from silicic acid raw materials, lime raw materials, and water. I ~ In a method of carrying out a synthesis reaction while heating and stirring the entire slurry to obtain an aqueous slurry of crystals to silicic acid calcinate, and forming and drying the aqueous slurry of crystals of calcinic silicate. -c1] 1 skin and alnini ``) tsu, ka α
It has been found that when a substance is added to the F↑ acidic liquid at a rate of 71..1' of crystals, the room temperature drying shrinkage of the resulting molded product is significantly lowered. In addition, in this study, the solid content of the raw material slurry was determined.

山皮を特定用共存せしめると、得られる珪酸カルシウム
成形体の曲げ強さも著しく大きくなり、また珪酸カルシ
ウム結晶スラリーに山皮を添加するととにより成形体の
曲げ強さ、焼成後の残存強度率が著しく向−トすること
が見出された。
When the specific coexistence of mountain skin increases the bending strength of the resulting calcium silicate molded product, and when the mountain skin is added to the calcium silicate crystal slurry, the bending strength of the molded product and the residual strength rate after firing increase. It was found that the

本発明しよこれ等新しい知見に基すき完成されている。The present invention has been completed based on new knowledge.

即ち本発明は珪酸原料と石灰原料とを山皮の共存下に水
に懸濁せしめて原料スラリーを調製]7、tW拌押下加
熱加圧して水熱合成反応せしめて珪酸bルシウム結晶ス
ラリーを得、次いでこれに料とイボ灰原料とを山皮の共
存Fまたけ不存在下に水に懸濁せしめて原料スラリーを
調製し、攪拌下に加熱加圧して水熱合成反応せしめて珪
酸力ルシウt、結晶ス:)す・−となし、次いで]11
1υ及びアル、ミニ「゛ツム化合物を添加して成形乾燥
するととを特徴とする珪酸カルシウム成形体の製法に係
るものである。
That is, in the present invention, a raw material slurry is prepared by suspending a silicic acid raw material and a lime raw material in water in the coexistence of mountain bark] 7. A hydrothermal synthesis reaction is carried out by stirring, pressing, heating and pressurizing with tW to obtain a b-lucium silicate crystal slurry. Next, a raw material slurry is prepared by suspending the raw material and privet ash raw material in water in the coexistence of mountain bark and in the absence of silicic acid. t, crystals:) su・- and pear, then] 11
The present invention relates to a method for producing a calcium silicate molded body, which is characterized by adding 1υ, Al, and mini-Tsum compounds and molding and drying.

本発明の大きなI特徴の一つし工珪酸llJルシウム結
晶ス5リーに+、l−+皮及びアル三ニウへ化合物を添
加するととである。これに依り得られる珪酸フコルシウ
ム成形体の常温に於ける乾燥収縮就中厚みjj向の乾燥
収縮が著L−’ <小さくなる。
One of the major features of the present invention is that compounds are added to engineered silicic acid 11 lucium crystal 3 +, 1-+ skins and aluminum 3. As a result, the drying shrinkage of the fucorcium silicate molded product obtained at room temperature, particularly in the direction of thickness jj, becomes significantly smaller than L-'.

本発明の他の大きなI特徴は原料スラリ・−に山皮をl
t!j定量即ち原料スラリーの固形分中KO,O1〜0
.4チ3有けしめるときは得られる成形体の+t1口・
y強さが入きくなると共K、山皮を珪酸ハルシウム結晶
スラリーに添加するときけ得られる成形体の焼成後の残
存強度が著しく向1=、−Jることである。
Another major feature of the present invention is to add mountain bark to the raw material slurry.
T! j Quantification, that is, KO, O1 to 0 in the solid content of the raw material slurry
.. When tightening 4 pieces 3, +t1 mouth of the obtained molded body.
As the y strength increases, the residual strength after firing of the molded product obtained when the husk is added to the halcium silicate crystal slurry increases significantly.

本発明をその製法に基すいて下:If、’= iで説明
rる。
The present invention will be explained below based on its manufacturing method: If,'=i.

先ず珪酸原t1、石灰原料及び水とから、まrはt−1
,−+皮を原料スラリー(で含有ぜ[2める(J、1合
に(ll]l+皮^から原料スラリ・−を’APd製−
する。珪酸原料としては結晶質\1しびに非晶質ト1酸
原料いずi]−も使用出来、前者としでt、1結晶質珪
酸を主成分とするものが広く使用出来、たとえば珪砂、
珪石、珪岩等を、また後者と17でr;I: :iF;
品質珪酸を主成分とする各種の非晶質珪酸が使用出来、
具体的にIr、またとえげ珪藻11.ホワイトカーボン
、シリカフラワー、シリコンづスト等を例示出来る。
First, from silicate source t1, lime raw material and water, mar is t-1
, - + skin is added to the raw material slurry (2).
do. As the silicic acid raw material, crystalline and amorphous silicic acid raw materials can also be used, and those whose main component is crystalline silicic acid can be widely used, such as silica sand,
silica, quartzite, etc., and the latter and 17 r;I: :iF;
Various types of amorphous silicic acid whose main component is quality silicic acid can be used.
Specifically, Ir, Mamagage diatom 11. Examples include white carbon, silica flower, and silicon dust.

一土たイ1灰原料としては各種の石灰原料が使用出来、
具体的にVま生石灰、消石灰、カーバイト滓等を挙げる
ととが出来る。山皮とは含水珪酸マづネシウΔ系鉱物で
あり、たとえば七[ニオライト、パリjルスjyイト、
アタパル、;トイトを代表例とL7で挙げることが出来
る。通常、マウンテンレザー、マウンテン」ルク、メル
シセム(海泡石)等と呼ばれ−もいるものである。オた
山皮幻−原右でもあるいけ市販品でもいずれでも良い。
Various lime raw materials can be used as the ash raw material.
Specific examples include quicklime, slaked lime, carbide slag, etc. Mountain bark is a hydrated silicate mineral, such as niolite, paris jyite,
Attapal and Toito can be cited as representative examples and L7. It is usually called mountain leather, mountain lux, meerschaum, etc. It can be either Otayamapi Gen-Gen-Usa or a commercially available product.

捷た山皮には−゛部炭酸ハルlシウム等が混入している
場合があるが、この゛様な場合にはこれを粉砕石(〈Q
」分離1−25で使用−1ものがtIltしい、との際
の111皮の添加量は原料スラリーの固形分に対し0.
0I〜0.4重h1チ好ましく Id O,03−0,
31tjf1tチfあ2)。コ(7)際(LOI市[豊
)チに達しない場、Piは得らノする成1[つ体の曲げ
強度の向)二が充分でυ;Yなく、゛まだ逆に0.4重
h1チよりも多くなると、同じく成形体の曲げ強Aが低
トする傾向がを)る。水it tit固形分に対し5重
量で15倍以ト好まL<1」18〜40倍程度である。
The shredded mountain bark may contain -partial halcium carbonate, etc., but in such cases, it can be crushed with crushed stone (Q
” When the 1-1 product used in separation 1-25 is too high, the amount of 111 skin added is 0.0% based on the solid content of the raw material slurry.
0I to 0.4 times h1, preferably Id O, 03-0,
31tjf1tchifa2). (7) When the end (LOI city [Yutaka)] is not reached, Pi cannot be obtained, the direction of the bending strength of the body is sufficient, υ; Y, and ゛ is still 0.4 When the weight is greater than 1 inch, the bending strength A of the molded product tends to decrease as well. It is preferably 15 times or more, preferably about 18 to 40 times (L<1), based on the weight of water and solids.

かくしで調製された原料スラリーは次いで檀ゼ(゛トー
加JT:加熱されて珪酸カルシウム結晶のスラリーとさ
れる。この際の条件し[飽和水蒸気圧5 Kq / c
ff!uトであり、反応時間はその蒸気圧並びに目的、
I−する珪酸)Jルシウム結晶の種類に応じ−(適宜に
選択さ)1、たとえば1−べII/ ’C’) −1’
 l−の場合飽和水蒸気用12Kz、/r+Jで3時間
、8にり”’ cJで6時間程度である。ま/こり・−
ノ1〜ライトの1烏合し」IQ5にり/′r−で2時間
、121くり、/ Craで4時間1’X IQ−で?
ある。
The raw material slurry prepared by hiding is then heated to form a slurry of calcium silicate crystals.
ff! The reaction time depends on its vapor pressure and purpose,
I - silicic acid) J Depending on the type of lucium crystal - (appropriately selected) 1, for example 1-beII/'C') -1'
In the case of l-, it takes 3 hours at 12Kz/r+J for saturated steam, and about 6 hours at 8"' cJ.
No 1 ~ Light's 1 combination" IQ5 Niri/'r- for 2 hours, 121 chestnuts, / Cra for 4 hours 1'X IQ-?
be.

この水熱合成反応に依り珪酸カルシウム結晶が多数絡合
してほぼ球状の二次粒子が多数水に分散上記二二次粒子
中に山皮が混入されていることと々る。
Due to this hydrothermal synthesis reaction, a large number of calcium silicate crystals are entangled to form a large number of approximately spherical secondary particles dispersed in water, and mountain bark is mixed into the secondary particles.

ト1t12の如く本発明に於いては珪酸カルシウム結晶
の二次粒子が多数水に分散した水性スラリーが製造さi
するが、この際使用する珪酸原料と石灰原料の種類の組
合せにより得られる上記二次粒子の密度が異なつ1−来
る。たとえば結晶質珪酸原料を使用する場合に於てd石
灰原料と[7て特に沈降容fiN 5 m1以上という
特殊な石灰乳を使用すると0.19 / tri程度の
軽量の一一次粒子も収得出来るという利点があり、また
上記の如く特殊な石灰乳を使用1〜ない場合は、(1,
1’i’ 、/ cJ程度の軒昂々ものは得がたく、こ
れよりも密度の大きい二次粒−子が収得出来る。また非
晶1!■珪酸原料を使用する場合して於いてけ通常の石
灰原1Nを使用し7でも0.lli’、/c−程fc)
−の軽石:な]二次粒子が収イ;)出来、止た江降各積
5mJLソ、]−というI:’ RL、:特殊な石灰乳
を使1トJ”ると実に密用004り/ cA稈程度いう
極めて超軽fitの一次お“ノ子がIIM得出来る。
In the present invention, an aqueous slurry in which a large number of secondary particles of calcium silicate crystals are dispersed in water is produced as shown in Figure 1t12.
However, the density of the secondary particles obtained differs depending on the combination of the silicic acid raw material and lime raw material used. For example, when using a crystalline silicic acid raw material, if you use a lime raw material and a special lime milk with a sedimentation volume fiN 5 m1 or more, it is possible to obtain lightweight primary particles of about 0.19/tri. There is an advantage that, as mentioned above, if special milk of lime is not used (1,
It is difficult to obtain particles as large as 1'i', /cJ, but secondary particles with a density higher than this can be obtained. Amorphous 1 again! ■When using silicic acid raw material, use normal limestone 1N and 0. lli', /c-modefc)
- pumice stone: ) Secondary particles were collected;) completed and stopped, each volume of 5 m JL,] - called I:' RL:: Using a special lime milk, 1 ton J" was secretly used.004 IIM can be obtained for extremely light-fitting first-order children, such as ri/cA culm.

沈降容積が太きいということtま石灰が白く水に分ハセ
I1、て安定な状態にあること即ら極免に細かい粒子t
り成り、従っ−C高いノラ応+<+を示−4−ことを意
味“する。沈降容積が5me以上の石灰乳を・製造する
Ji法自体QJ二義的なものであり特に制限されない。
The fact that the sedimentation volume is large means that the lime is white and separates into water, and that it is in a stable state, which means that the particles are extremely fine.
Therefore, it means that -C indicates a high nola reaction +<+.The Ji method for producing milk of lime with a sedimentation volume of 5 me or more is itself secondary to QJ and is not particularly limited.

、この石灰乳の沈降容積は原料と1−るイー1灰イ1自
体、石灰製潰時の焼成温度、石灰を水に消和−Jるとき
の水の量、そのときゃ温度、そのときの攪拌条f′1等
(て)1°右され、17I)中消和時の湛1([、]i
lびに]冑拌条件妬」、す(きく影響布受に’)’ 、
’E+が、いずilにせよ通常σ)r1灰乳の製造方法
でf+;t f1的と七る沈、降tf積5 ml以1・
の石灰乳苓イ1することは114j来ない。而しC沈降
容fl(5mll以内71i灰乳にJ、例えば代表的に
υJ、水利石灰分(固形分)比を5倍(重用)以上とし
て野牛し5くは60℃以上の温度で高速乃至強力攪拌す
るか、またン;]湿式磨砕機を利用して湿式磨砕し、こ
hを静償分散さ辻れは良い。たとえばホ七五士(1−の
如き激L7い撹拌によって上記所望の石灰乳を収得出来
る。攪拌速度並びに攪拌強さは攪拌時の温度を高くしで
並びに時間を長くすれば一般にドげることが出来る。た
とえば20℃で消和した石灰乳でもこれを長時間ホ七ミ
十41−で撹拌すると所期の石灰乳とすることが出来る
。また檀拌機としrは各種のものが使用され邪魔板を有
1〜でいるものでも又はこれの無いものでも使用出来る
, the sedimentation volume of this milk of lime is based on the raw materials, the ash itself, the firing temperature during lime crushing, the amount of water used to slake the lime with water, the temperature at that time, and the temperature at that time. Stirring line f′1 etc. (te) 1° right, 17I) during quenching 1 ([,]i
``I'm jealous of the conditions that affect me'', ``I'm jealous of the conditions that affect me'',
'E+ is usually σ)r1 in the production method of ash milk;
114j does not come to the limestone milk 1. Then, C sedimentation volume fl (within 5 ml) 71i J to ash milk, for example, υ J, water use lime content (solid content) ratio of 5 times (heavy use) or more, wild cow 5 or high speed at a temperature of 60 ° C or more Wet grind using a wet grinder to disperse the powder. For example, by stirring vigorously as in Milk of lime can be obtained.The stirring speed and strength can generally be reduced by increasing the temperature and stirring time during stirring.For example, even if milk of lime has been slaked at 20°C, if it is left for a long time. The desired milk of lime can be obtained by stirring with a ho-7mi-ju 41-.In addition, various kinds of agitators are used, and those with or without baffle plates can be used. I can do it.

本発明圧於いてはかくして得られた珪酸)]ルシウt、
結晶スラリー1(アルミニウム化合物を添加する。この
際使用されるアルミニウム化合物とじでは珪酸カルシウ
ム結晶と反応して水不溶性乃至難溶性のフコルシウム塩
を生成する化合物が使用出来、たとえば硫酸711ノミ
二〇へ(無水塩及び含水塩をnむ)、リシ酸アル′F、
:つΔ、すυ酸水素アルミニウム等を例示出来る。こi
1等アルエ三ウつ化合物in 結晶スラリー中の固形分
及びアルミニr″i /、 化合物の合削重損中に無水
物基準で1〜15重用チ好まり、 < tj: I〜1
o重M%程度添加する。この際Pルミニウム化合l吻の
添加量が1重郊チに達しない場合は所期の効果が期待1
.4!1G <、才だ15重M弼より多く々ると、乾燥
収縮が逆にノ、、:きくなる傾向がある。
In the process of the present invention, the silicic acid thus obtained)]
Crystal slurry 1 (Add aluminum compound. In the aluminum compound binder used at this time, a compound that reacts with calcium silicate crystals to produce a water-insoluble or sparingly soluble fucorcium salt can be used. For example, to sulfuric acid 711 No. 20 ( (including anhydrous salts and hydrated salts), ricylic acid Al'F,
: Δ, aluminum hydrogen sulfate, etc. can be exemplified. Koi
Solid content in crystal slurry and aluminum r″i /, 1 to 15 weight compounds on anhydride basis during compound cutting and weight loss, < tj: I to 1
Add approximately 0% by weight M%. At this time, if the amount of P-luminium compound added does not reach 1%, the expected effect is expected to be 1.
.. 4!1G <、If it is more than 15 weight M, the drying shrinkage tends to become worse.

′!)だ本発明に於いては珪酸カルシr’)ム結晶スラ
リーに山皮を添加するととも出来る。この添加によりイ
(Iられろ成LEニ体の焼成後の残(1強1隼を向I−
け−し7めることが出来る。この際+、11皮(りj結
晶ス″′51−J −中の固形分及び山皮の合計重量中
KO,4〜15重f11係稈度である。
′! ) In the present invention, it is also possible to add mountain bark to the calcium silicate crystal slurry. By this addition, the residue after firing of the formed LE body (1 strong 1 Hayabusa)
It is possible to set a limit of 7. At this time, the total weight of the solid content in the crystals and the husk is KO, 4 to 15 weights, and the culm degree is 11.

この際()、4重用)係に達り、々い鳴合しI+t’t
l:効果が充分発揮されず、また15重i4%よりも多
くなっでもより以I−の効果i+期期用出来いばかりで
なく、A−”h−IIの増大につれて成形体の乾燥収縮
が犬き(なる傾向があり好−ましくない。この様に珪酸
カルシバツム結晶の水tlスラリーに山皮を添υ]1す
る場合+lJ山皮は珪酸ノコルシウム結晶の二次粒子内
にはイア在せず、該丁次粒子と接[7で1/こけ接せず
に水中に均一に分散[7ている。
At this time, I reached the person in charge of (), quadruple duty) and shouted
l: The effect is not sufficiently exhibited, and even if the amount is more than 15% i4%, the effect of I- is not only achieved in the i+ period, but also the drying shrinkage of the molded product increases as h-II increases. It is undesirable as it tends to cause a scorching effect.In this way, if you add the lint to the water slurry of the calcium silicate crystals, the lint will be present in the secondary particles of the nocolsium silicate crystals. First, it is uniformly dispersed in water without coming into contact with the particles [7].

本発明に於いては珪酸カルシウム成形体に通常の添加料
を含有ぜしめることが出来、この際の添加料としては従
来から使用されて来たものがいず11も使用出来、たと
えば繊維質物質、粘土類、セ:I :、、i l−1」
[コイタルシリハ、アルミすりIl/ 等を例示出来、
史に詳しくは繊維質物質としては石綿、岩綿、15ラス
繊維、セラミックファイバー、炭素繊維、金属繊維等の
無機質繊維、ボリア三ド、ポリゴーステル等各種合成繊
維やパルづ、ゼルロース等の各種天然繊維の如き有機質
繊維を例示出来、また粘土類と[7てばたとえばカオリ
シ、−ベシ1ヘナ。
In the present invention, the calcium silicate molded article can contain ordinary additives, and in this case, any of the additives that have been conventionally used can be used, such as fibrous materials, Clays, Se:I:,,i l-1''
[Koitarushiriha, Aluminum Grip Il/ etc. can be given as examples,
In more detail, fibrous materials include asbestos, rock wool, 15 lath fibers, ceramic fibers, carbon fibers, inorganic fibers such as metal fibers, various synthetic fibers such as boriatrido and polygostel, and various natural fibers such as Palzu and Xelulose. Examples include organic fibers such as clays, and clays, such as kaorishi and henna.

(+−、パーf O−フィー5yト等を、セメントとし
てけたと乏、げポルドラυドセメzノド、P 11/ 
、′士t′4.ン1−1石青等を例示出来る。これ等添
加t(を含有せしめる手段としでは、原料スラリーに添
加1」を添ツノ[1する手段(以下先入れ手段という)
と、旧l−+ルシウム結晶スラリーに添加1Jを添加す
る手段(後入れ手段という)とがあり、先入れ手段の禍
合は通常無機質繊組が使用され、後入11手段σ)鳩i
 u y= <各種の添加材が使用出来る。
(+-, parf O-fee 5yt, etc., as cement, gepoldora υ docemez nod, P 11/
,'shit'4. Examples include N1-1 Sekisei and the like. As a means for containing these additives, there is a means for adding an additive 1 to the raw material slurry (hereinafter referred to as a pre-adding means).
and a means for adding 1 J to the old l-+ lucium crystal slurry (referred to as a post-adding means).In the case of the pre-adding means, inorganic fibers are usually used, and 11 post-adding means σ) pigeon i
u y= <Various additives can be used.

(扶下((月’ %+λ例並びに比較例を示1.て本発
明を具イセ的に説明するが、下記例に於いて部f/こに
IチとあるrI: f侍にことわらないかき゛り重h:
ぞl! +、−fr−rJ、重11(チを示す。
The present invention will be specifically explained with reference to examples and comparative examples. No need to worry:
Wow! +, -fr-rJ, heavy 11 (indicates H).

実MH1((II  1 生イ1灰((7゛σ(λQ5.0チ)41.42部を8
0χ゛の温水497部中で消和しでイ(また石灰乳の?
′1−降容積kj−1.5ra7′−でrあつブこ。1
−記石灰乳にf−1,0518合1((0,(1592
係)のセピオライ1〜(中国産)を2oO11ヤ計倍の
水でミ士す・−てで2分間分散させ474Nk。
Real MH1 ((II 1 raw i 1 ash ((7゛σ(λQ5.0chi)) 41.42 parts to 8
It is slaked in 497 parts of 0x゛ warm water (also lime milk?
'1-falling volume kj-1.5ra7'- and r hot. 1
- Add lime milk to f-1,0518 go 1 ((0, (1592
Disperse Sepiolai 1~ (produced in China) of 2000-11 times the total amount of water for 2 minutes at a mixer to make 474Nk.

ス゛)リーとSV均均粒径径025μmのフよりシリ」
シ櫂ス1(810291,5%) 46.08部を20
重量倍の水でiji E E士+J−にて2分間分散さ
せて得たスラリーを加4−1咀に水を加えて全体の水量
を固形分の24重量倍となるように混合して原料スラリ
ーを得た。次いでこれらを飽和水蒸気圧l5Ks+/c
a、温度200.4℃でオートクレーづ中で回転数4O
r、p、mf攪拌翼全回転しながら2時間水熱合成反応
を<1つて結晶スラリーを得た。これらの結晶スラリ・
−を100℃で24時間乾燥してX線回折分相し7た所
、・ノーノドライ1−結晶であることを確認り、、 7
’/1.。
"Sri" and "SV" have an average particle diameter of 025 μm.
Sis Paddle 1 (810291,5%) 46.08 parts to 20
Add the slurry obtained by dispersing the slurry for 2 minutes with twice the weight of water using an Iji E E + J-, add water to 4-1 times the weight, and mix so that the total amount of water is 24 times the weight of the solid content. Got slurry. Next, these are saturated water vapor pressure l5Ks+/c
a. Rotation speed 40 in an autoclay at a temperature of 200.4℃
A hydrothermal synthesis reaction was carried out for 2 hours while r, p, mf stirring blades were rotated at full rotation to obtain a crystal slurry. These crystal slurries
- was dried at 100℃ for 24 hours and subjected to X-ray diffraction phase separation, and it was confirmed that it was a non-dry 1-crystal.
'/1. .

次いで、上記結晶スラリーに、スラリー中の固形分を基
準とI7、添加材としてj3ラス繊#7部、パル15部
、ポルl〜ラシドセメント3部及び硫酸Pルミニウム含
水塩(At2(5OZl )3・l 81120 、、
)を無水物基準で下記第1表に示される比率で加えてづ
゛1ノス成形し1.120℃で20時間乾燥して成形体
を得た。得られた成形体の物性にI、−上記第1表の通
りであった。
Next, to the above crystal slurry, I7 based on the solid content in the slurry, 7 parts of j3 lath fiber #, 15 parts of pal as additives, 3 parts of pol l~rashid cement, and hydrated Pluminium sulfate (At2(5OZl)3) were added to the crystal slurry.・l 81120,,
) were added in the proportions shown in Table 1 below on an anhydride basis, molded in one batch, and dried at 1.120°C for 20 hours to obtain a molded product. The physical properties of the obtained molded article were as shown in Table 1 above.

第1表 残存強度率は下記式によって求めた。Table 1 The residual strength rate was determined by the following formula.

実施例 生石灰(CaO95,0% ) 41.42部を80℃
゛ノ潟水497部中で消第11(〜て得た5灰乳の沈降
容fIf k14.4mlであった。上記石灰乳に平均
粒子径(1,25fimの一7IOE/す]、/ダスト
(St O291,5% )4608部を20重鼠倍の
水でホ′f:ヱクサーにて2分間分散させて得たスラリ
・−を加え、更に水を加えて全体の水昂を固形分の24
重量倍となるように混合(7て原料スラリーを得た。次
いでこれを飽和水蒸気圧15に9/cJ、温度200.
4℃で」−1−クレーづ中で回転数4 Q r、p、m
で攪拌翼を回転しながら2時間水熱合成反応を行って、
リーノトライト結晶よりなるスラリーを得た。
Example 41.42 parts of quicklime (CaO95.0%) at 80℃
The sedimentation volume of the 5 ash milk fIf k14.4 ml was 14.4 ml. Add the slurry obtained by dispersing 4608 parts of (St O291.5%) in 20 parts of water for 2 minutes in an extractor, and then add water to adjust the total water content to the solid content. 24
A raw material slurry was obtained by mixing to double the weight (7).Then, this was heated to a saturated water vapor pressure of 15/cJ and a temperature of 200.
At 4°C - 1 - Number of revolutions in clay 4 Q r, p, m
A hydrothermal synthesis reaction was carried out for 2 hours while rotating the stirring blade.
A slurry consisting of linotrite crystals was obtained.

次いで上記結晶スラリーに、スラリー中の固形分を基準
と1〜、添加料としてj3ラス繊維7部、バルー55部
、ポルトランドセメシト3部及び硫酸アルミニウム含水
塩(At2(So、、)、:、J・18H20)を無水
物基準で及び所定昂のtヒオライl−(中国産、炭酸カ
ルシウムが−・部混在している)を100重量倍の水で
可+4j−にて2分間分散させて得たスラリーを第2表
に示される[)c率で加えて、づレス成形り、、120
℃で20時間乾燥して成形体を得た。
Next, to the above crystal slurry, 1 to 7 parts of J3 lath fiber, 55 parts of Balu, 3 parts of Portland Cemecite, and aluminum sulfate hydrate (At2 (So, ), :, J・18H20) was obtained on an anhydride basis by dispersing a specified amount of t-hyolite (produced in China, containing -. part of calcium carbonate) in 100 times its weight of water at +4j- for 2 minutes. Add the slurry at the ratio [)c shown in Table 2, and form it into a zuress, 120
A molded article was obtained by drying at ℃ for 20 hours.

7替られた成形体の物性けTF第2表の通りであった。The physical properties of the molded article were as shown in TF Table 2.

第  2  表 但しA I 、 A、 l l及びAi I 2 il
l比較イノ・11を示゛1゜尚硫酸ア11ノミπつへ含
水用&;i: I 0%の水溶液で添υ++Lだ。
Table 2 Provided that A I , A, l l and Ai I 2 il
l Comparison Ino 11 is shown. 1゜ Sulfuric acid a11 is added for water content &; i: I 0% aqueous solution is added υ++L.

実施例 3 tp゛石灰((、’a095.4%) 45.83部を
80℃の温水550部中で消和し、ホ℃ミタサーにて3
分間水中で分散させて得た石灰乳の沈降容積は18.5
m/′であった。−)1記石灰乳に平均粒子径9μmの
珪石粉末(St 0294.06%) 49.63部を
加え、更に水を加えて全体の水損を固形分の22重溺倍
となるように混合して原料スラリーを得た。次いでこれ
を飽和水蒸気圧15Kq/CJ、温度200 、4℃で
オートクレーづ中で回転数41 r、p9mで攪拌翼を
回転(−ながら2時間水熱合成反応を行って、す・−ド
ライド結晶よりなるスラリーを得た。
Example 3 45.83 parts of tp lime ((,'a095.4%) was slaked in 550 parts of warm water at 80°C, and heated in a thermometer at 3°C.
The sedimentation volume of milk of lime obtained by dispersing in water for 18.5 minutes is
m/'. -) Add 49.63 parts of silica powder (St 0294.06%) with an average particle size of 9 μm to the milk of lime in step 1, and then add water to mix so that the total water loss is 22 times the solid content. A raw material slurry was obtained. Next, this was subjected to a hydrothermal synthesis reaction for 2 hours while rotating the stirring blade at a rotation speed of 41 r and a pg of 9 m in an autoclave at a saturated water vapor pressure of 15 Kq/CJ, a temperature of 200, and a temperature of 4°C. A slurry was obtained.

次いて上記結晶スラリーに、スラリー中の固形分を基準
とし、添加料としてjJシラス維7部、パル15部、ポ
ル1−ランドセメ、J+−3部及び各種アルミニウム化
合物を無水物基準で及び所定JiのセLこ1ライl−’
(代用薬品製、商品名、■・−ドーヲラスAf L −
1001) )を+00重Nt倍の水で2士41−にて
29部間分散させて得たス5リーを第3表に示される比
率で加えて、づレス成形し、! 2 (1℃で20時間
乾燥して成形体を(!J ;#。Y!)ら′iまた成形
体のI物性は下記第3表の通りであった。
Next, to the above crystal slurry, based on the solid content in the slurry, as additives, 7 parts of jJ shirasu fiber, 15 parts of Pal, Pol 1-Landseme, J + - 3 parts, and various aluminum compounds are added on an anhydride basis and at a predetermined Ji. No se L this one lie l-'
(Made by substitute medicine, product name, ■・- Doworas Af L -
1001) ) was dispersed in 29 parts with +00 weight Nt times water at a temperature of 2-41- to add 35% at the ratio shown in Table 3, and form the mixture into a zuresu form. 2 (Dried at 1° C. for 20 hours to obtain a molded product (!J; #.Y!).The physical properties of the molded product were as shown in Table 3 below.

/″ 、、/’ /・″ / /’ S?ノに2〜7に於いてアルミニウム化合物は10チの
水溶液若しくはl腎濁液の状態で添加し7フこ。
/″ 、、/' /・″ / /' S? In steps 2 to 7, the aluminum compound was added in the form of 10 g of aqueous solution or 1 g of renal suspension.

実施例 4 石灰乳の沈降容積が41.3mlのものを用いる以外は
実施例3と同様にニジて合成I−だ〜フ・−ノ1−ライ
ト結晶スラリ・−に、スラリー中の固形分を基準とし、
添加i(、=して15ラス絆i訂17部、バルーづ5部
、ボルトランドセメシ1−3部及び硫酸アルミニウム含
水均(・t〕2 (S01+ )3・l81120)を
無水物フ1(準−ζ゛及び2部のせ1τオライド(中国
産) ’、f、 l 00重fit倍の水でミ±43−
  )7で2分間分散させ−し得たスラリーを第4表に
示される比率で加乏−て、′51ノス成形(〜、120
て゛で20時間乾燥11.て成形体を1()だ。
Example 4 The solid content in the slurry was added to the synthetic I-F-no-1-lite crystal slurry in the same manner as in Example 3 except that milk of lime with a sedimentation volume of 41.3 ml was used. As a standard,
Addition i (, = 15 russian i edition 17 parts, Baluzu 5 parts, Bortland Semesi 1-3 parts and aluminum sulfate water content (・t〕2 (S01+) 3・l81120) was added to the anhydride fu 1 ( Quasi-ζ゛ and 2 parts of 1τ olide (produced in China) ', f, l 00 times the weight of water to mix ±43-
) 7 for 2 minutes, the slurry was enriched and enriched at the ratio shown in Table 4, and '51 Nos. molding (~, 120
Dry for 20 hours 11. The molded body is 1().

得t−)J)だ成J(を休のrlj、rr性は下配第4
火&)1i(iりであった。
Toku t-) J) Dase J
Tuesday &) 1i (It was iri.

第4表 イ!’、 L yf61は比較例6−示−ン。Table 4 stomach! ', Lyf61 is Comparative Example 6-in.

又A2〜4に於いてd硫酸アルミニつへ含水塩を10%
の水溶液で添加した。
In addition, in A2-4, add 10% hydrated salt to aluminum sulfate.
It was added as an aqueous solution.

(以 十)(hereafter 10)

Claims (1)

【特許請求の範囲】[Claims] (1)珪酸原料J゛石灰原岑1とを山皮の共存下に水に
懸濁せI−めで原料スラリーを調製t7、檀、押下に加
熱加圧して水熱合成反応せしめて珪酸カルシウム結晶ス
ラリーを得、次いでこれにアルミニr″ツム化合物を添
加し成形乾燥することを特徴とする珪酸ハルシウム成形
体の製法。 (治 珪酸原料と石灰原料とを山皮の共存下または不存
在下に水に懸濁せ17めて原料スラリーを調製り、、伶
押下に加熱加圧して水熱合成反応忙しめて珪酸カルシウ
ム結晶スラリーとなし、次いで山皮及びアルミニウム化
合物を添加して成形乾燥することを特徴と1−る珪酸カ
ルシウム成形体の製法。
(1) A raw material slurry is prepared by suspending the silicic acid raw material J and limestone 1 in water in the coexistence of mountain bark. A method for producing a halcium silicate molded article, which is characterized by obtaining a slurry, then adding an aluminum r''tum compound thereto, and molding and drying it. 17 to prepare a raw material slurry, heat and pressurize under pressure to carry out a hydrothermal synthesis reaction to form a calcium silicate crystal slurry, then add mountain bark and an aluminum compound and form and dry. 1. A method for producing a calcium silicate molded body.
JP12942582A 1982-07-23 1982-07-23 Manufacture of calcium silicate formed body Granted JPS5921558A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12942582A JPS5921558A (en) 1982-07-23 1982-07-23 Manufacture of calcium silicate formed body

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12942582A JPS5921558A (en) 1982-07-23 1982-07-23 Manufacture of calcium silicate formed body

Publications (2)

Publication Number Publication Date
JPS5921558A true JPS5921558A (en) 1984-02-03
JPH0158147B2 JPH0158147B2 (en) 1989-12-08

Family

ID=15009175

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12942582A Granted JPS5921558A (en) 1982-07-23 1982-07-23 Manufacture of calcium silicate formed body

Country Status (1)

Country Link
JP (1) JPS5921558A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63107851A (en) * 1986-10-24 1988-05-12 三井東圧化学株式会社 Heat-resistant hydraulic cement material and manufacture
JPS63107852A (en) * 1986-10-24 1988-05-12 清水建設株式会社 Sea water-resistant cement material and manufacture of sea water-resistant mortar or concrete

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MXPA05004969A (en) * 2002-11-05 2005-08-02 James Hardie Int Finance Bv Method and apparatus for producing calcium silicate hydrate.

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63107851A (en) * 1986-10-24 1988-05-12 三井東圧化学株式会社 Heat-resistant hydraulic cement material and manufacture
JPS63107852A (en) * 1986-10-24 1988-05-12 清水建設株式会社 Sea water-resistant cement material and manufacture of sea water-resistant mortar or concrete

Also Published As

Publication number Publication date
JPH0158147B2 (en) 1989-12-08

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