JPS5969461A - Sintered porous ceramic product - Google Patents

Sintered porous ceramic product

Info

Publication number
JPS5969461A
JPS5969461A JP58165836A JP16583683A JPS5969461A JP S5969461 A JPS5969461 A JP S5969461A JP 58165836 A JP58165836 A JP 58165836A JP 16583683 A JP16583683 A JP 16583683A JP S5969461 A JPS5969461 A JP S5969461A
Authority
JP
Japan
Prior art keywords
weight
molded article
molded body
clay
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.)
Pending
Application number
JP58165836A
Other languages
Japanese (ja)
Inventor
ハンス・レンナ−ト・スリツケ
ギヨ−テ・バルデマ−ル・ノ−ルブランド
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.)
ANTIPHON AB
Original Assignee
ANTIPHON AB
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 ANTIPHON AB filed Critical ANTIPHON AB
Publication of JPS5969461A publication Critical patent/JPS5969461A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B38/00Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof
    • C04B38/10Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof by using foaming agents or by using mechanical means, e.g. adding preformed foam
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B38/00Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof
    • C04B38/02Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof by adding chemical blowing agents

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Compositions Of Oxide Ceramics (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)
  • Separation Using Semi-Permeable Membranes (AREA)
  • Porous Artificial Stone Or Porous Ceramic Products (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】 〔発明の関連する技術分野〕 この発明は焼結された多孔性セラミック成形体に関する
DETAILED DESCRIPTION OF THE INVENTION [Technical field to which the invention relates] This invention relates to a sintered porous ceramic molded body.

(従来技術〕 珪灰石(珪酸カルシウム)、燐酸水素アルミニウムおよ
び水を主成分とする混合物から多孔性セラミック材料を
製造することはすでに米国特許第314899(3号に
より公知であるが、この公知の酸塩基系により調製され
たセラミック材料を乾燥し焼成することは極めて面倒な
ことが判っている。このだめ広範囲の乾燥亀裂が製品に
生じるのが普通で、場合によっては製品が焼結時に破れ
てし1うことがある。
PRIOR ART The production of porous ceramic materials from mixtures based on wollastonite (calcium silicate), aluminum hydrogen phosphate and water is already known from US Pat. No. 314,899 (3); Drying and firing ceramic materials prepared by base systems has proven to be extremely tedious. Extensive drying cracks are common in the product, and in some cases the product may tear during sintering. There is one thing.

この問題のため今までこの製品を焼結することを避けて
来だが、乾燥しただけの製品は強度が低過ぎて商業価値
がない」二、その乾燥時の亀裂のため多くを廃棄する必
要があった。
Due to this problem, we have avoided sintering this product until now, but the strength of the dried product is too low to be of commercial value.2) Many have to be discarded due to cracking during drying. there were.

従って上記米国特許による酸塩基方式は何等商業価値の
ある製品をもたらしていない。
Therefore, the acid-base method according to the above US patent has not resulted in a product of any commercial value.

本来この焼結多孔性セラミック材料の製造を可能ならし
めることは高温における熱や音の絶縁用として極めて必
要である。すなわち焼結したセラミック材料はいくつか
の特長を有し、“例えば高温に1制え、通常他の材料を
強く腐食する普通の化学薬品(でよって侵されない。
It is extremely necessary to be able to manufacture this sintered porous ceramic material for use in heat and sound insulation at high temperatures. Thus, sintered ceramic materials have several characteristics, such as being able to withstand high temperatures and being not attacked by common chemicals that normally strongly corrode other materials.

〔発明の開示〕[Disclosure of the invention]

上記公知の酸塩基方式による問題はこの発明により解消
され、焼結した多孔性セラミック成形体が提供される。
The problems caused by the known acid-base method described above are solved by the present invention, and a sintered porous ceramic molded body is provided.

その成形体は次の成分から成る組成物から製造される。The molded body is manufactured from a composition consisting of the following components:

(1)  珪酸カルシウムおよび/またはアルミン酸カ
ルシウムのような1種またはそれ以上の塩基性材料。
(1) One or more basic materials such as calcium silicate and/or calcium aluminate.

(2)  次式て表される1種またはそれ以上の化合物
の水溶液。
(2) An aqueous solution of one or more compounds represented by the following formula.

XAl2O3・yP205.zH20 但し、0.3工x9.1工y≦転 1工2≦10、好ま
しくは、x−1、y−3、z=3゜(3)  粘土まだ
はカオリン。
XAl2O3・yP205. zH20 However, 0.3 work x 9.1 work y≦turn 1 work 2≦10, preferably x-1, y-3, z = 3° (3) Clay is kaolin.

(4)  長石 (5)  シリカおよび/まだは燐酸アルミニウム。(4) Feldspar (5) Silica and/or aluminum phosphate.

(6)  随意の水。(6) Voluntary water.

この組成物は成形体を乾燥し最後に焼結するが、硬化前
に気泡を内部に持ったまま化学反応により硬化して多孔
性成形体となるようになっている。
This composition is dried into a molded body and finally sintered, but before hardening, the composition is hardened by a chemical reaction with air bubbles inside to form a porous molded body.

この組成物は成分+1)、(2)の内容により化学反応
によって室温で硬化する。これは通常具なる物質を混入
した後30分以内に起り、従って外部から熱を供給する
必要はない。
This composition cures at room temperature by a chemical reaction depending on the contents of components +1) and (2). This usually occurs within 30 minutes after incorporation of the ingredients, so there is no need for external heat to be supplied.

この発明の適当な実施例によると、成分(1)が珪灰石
から成り、これが成分(2)の燐酸水素アルミニウム水
溶液と反応する。この燐酸水素アルミニウム水溶液は次
式に従って化学量論的に水酸化アルミニウムAZ(OH
)3を85%のオルト燐酸H3PO4に溶解して製する
のがよい。
According to a suitable embodiment of the invention, component (1) consists of wollastonite, which reacts with component (2), an aqueous aluminum hydrogen phosphate solution. This aluminum hydrogen phosphate aqueous solution is stoichiometrically converted into aluminum hydroxide AZ(OH
)3 in 85% orthophosphoric acid H3PO4.

7u+(OH)3+3H3P04→AI!(H2PO4
)、+3H20+熱最終混合物の粘度が高くなりすぎな
いように、大抵の場合反応後溶液に水を力(1える。
7u+(OH)3+3H3P04→AI! (H2PO4
), +3H20+heat In most cases, water is added to the solution after the reaction to prevent the viscosity of the final mixture from becoming too high.

珪灰石は塩基性反応をする珪酸カルシウムで、組成物が
硬化するとき起る化学反応においてカルシウムイオン浸
透のだめAJ(H,、PO4)、  と燐酸カルシウム
の析出を生ずる。珪酸カルシウムの代りにアルミン酸カ
ルシウム捷たは珪酸カルシウムとアルミン酸カルシウム
の混合物を用いることもてきる。
Wollastonite is a calcium silicate that reacts with basicity, and in the chemical reaction that occurs when the composition hardens, calcium ion penetration results in the precipitation of AJ (H,, PO4) and calcium phosphate. Calcium aluminate or a mixture of calcium silicate and calcium aluminate may be used instead of calcium silicate.

上記成分(3)、+4)、+5]は組成物をはX′ポー
セレンペーストの様に問題なく乾燥および焼成し1qる
ようにする。
Ingredients (3), +4), +5] enable the composition to dry and bake without problems like X' porcelain paste.

この発明の1実施例では、成分(3)が粘土から成り、
成分(5)が石英(シリカ)から成り、成分(4)の長
石ど共に焼結時にガラスイ目を形成する。このガラスl
[′4は石英のような砕石状飼料を結着して粒子間に極
めて強力な結合を形成する。長石はカリウム長石がよい
In one embodiment of the invention, component (3) comprises clay;
Component (5) consists of quartz (silica), and forms glass eyes when sintered together with the feldspar of component (4). this glass
['4 binds crushed stone feed such as quartz to form extremely strong bonds between particles. The best feldspar is potassium feldspar.

石英の代りに結晶形の異なる無定形5i02のような5
102も使用することができる上、」二連のようにその
シリカの一部寸たは全部を燐酸アルミニウムで置換する
こともできる。
Amorphous 5 such as 5i02 with a different crystal shape instead of quartz
102 can also be used, as well as some or all of the silica can be replaced with aluminum phosphate, as in the case of 2 series.

ガラス相内には普通焼成により燐酸3石英Ca3(PO
4)2が形成されている。
In the glass phase, phosphoric acid triquartz Ca3 (PO
4) 2 is formed.

成形体は温度800〜1500°C1好捷しくけ100
0〜1300°Cの焼成により焼結される。
The temperature of the molded body is 800 to 1500°C, and the temperature is 100°C.
It is sintered by firing at 0 to 1300°C.

この発明によるセラミック成形体の製造に用いられる組
成物の各種成分の比率は広範囲に変えることができるが
、普通は次の通りである。
The proportions of the various components of the compositions used in the production of ceramic molded bodies according to the invention can vary within a wide range, but are typically as follows.

(1)珪酸カルシウムおよび7才たけアルミン酸カルシ
ウム10〜65、シばしくば10−40、好寸しくけ2
0〜65重量%。
(1) Calcium silicate and 7-year-old calcium aluminate 10-65, Shibashikuba 10-40, Kosun-shikake 2
0-65% by weight.

(2)次式の化合物1種まだはそれ以」−5〜40重量
%。
(2) One or more compounds of the following formula -5 to 40% by weight.

x Al2O2−y P2O,、・z H20<<<<
<< 但し、0.3=x=3.、  I=y=6、I=z==
IJ好ましくは、x−1、y−3、Z−3゜(3)  
粘土まだはカオリン5〜30重量%。
x Al2O2-y P2O,, z H20<<<<
<< However, 0.3=x=3. , I=y=6, I=z==
IJ preferably x-1, y-3, Z-3° (3)
Clay still contains 5 to 30% kaolin by weight.

(4)  長石1〜10重量%。(4) 1-10% by weight of feldspar.

(5)  シリカおよび/または燐酸アルミニウム10
〜40重量・%0 以」二すべで組成物の乾燥状態で計算する。
(5) Silica and/or aluminum phosphate 10
~40% by weight 0 or less'' Calculated based on the dry state of the composition.

この発明による多孔性成形体を得るだめに他の方法を用
いることもできる。例えば発酵法を用い、発酵Allを
加えて所要の多孔度を得ることもできる。
Other methods can also be used to obtain porous molded bodies according to the invention. For example, fermentation methods can be used and fermented All may be added to obtain the desired porosity.

また空気注入または発泡剤との攪拌も有効な方法である
。まだガス発生剤を用いるのも適当て、この発生剤の例
としては炭酸マグネシウムのような炭酸塩や、アルミニ
ウム、鉄のような金属がある。
Injection of air or stirring with a blowing agent is also an effective method. It is also appropriate to use gas generating agents, examples of which include carbonates such as magnesium carbonate, and metals such as aluminum and iron.

炭酸塩添加剤例えば塩基性炭酸マグネシウムに発泡剤と
泡安定剤を加えて強く攪拌すると、成形体内に良好な細
胞状組織ができることが判っだ。
It has been found that adding a foaming agent and a foam stabilizer to a carbonate additive, such as basic magnesium carbonate, and stirring vigorously creates a good cellular structure within the molded body.

この細胞の体積や大きさはその発泡法を種々変えること
により変えることができる。
The volume and size of the cells can be changed by changing the foaming method.

どの発泡法を用いるかはこの発明の重蟹項[1てはない
が、組成物の硬化が終るまでに所要の細胞組織が形成さ
れることがあらゆる場合に必要と考えられる。
The foaming method to be used is not an important aspect of the present invention, but it is considered necessary in all cases that the required cell tissue be formed by the time the composition is completely cured.

場合によっては組成物に界面活性剤を加えることが適当
である。
It may be appropriate to add surfactants to the composition.

焼結前の成形体はその一1寸で強度が極めて高いた−め
、問題なしにベルトで搬送したり炉内や架台」二に積」
二げることができ、寸だ機械的強度も化学的強度も大き
いだめ焼結なしで使用することもできる。しかし焼結後
は多孔性成形体の性質が極めて良くなる。すなわち機械
的性質が優れている上、薬品その他の腐食性物質に極め
て高い抵抗を示す。
The compact before sintering is 11 inches long and extremely strong, so it can be transported on a belt or stacked in a furnace or on a stand without any problems.
It can be used without sintering because it has very high mechanical and chemical strength. However, after sintering, the properties of the porous compact become significantly better. In other words, it not only has excellent mechanical properties but also exhibits extremely high resistance to chemicals and other corrosive substances.

その」二この成形体は吸音性および断熱性が優れている
Second, this molded body has excellent sound absorption and heat insulation properties.

この発明による成形体は多くの特長を有するだめ種々の
目的に使用することができる。例えば自動車の消音器の
吸音部品として1個寸たけそれ以上の成形体を使用する
こともできる。この成形体口、寸だ曲の吸音目的に使用
し得ることも勿論であるが、建築用ブロック、フィルタ
、各種断熱材のような他の目的にも使用することができ
る。
The molded article according to the invention has many features and can be used for various purposes. For example, molded bodies of one size or more can also be used as sound-absorbing parts for automobile silencers. Of course, this molded body mouth can be used for the purpose of absorbing sound in curves, but it can also be used for other purposes such as building blocks, filters, and various heat insulating materials.

〔発明の実施例〕[Embodiments of the invention]

次にこの発明を種々の組成物を用いた焼結多孔性成形体
の製法を示す実施例について説明する。
Next, the present invention will be described with reference to examples showing methods for producing sintered porous molded bodies using various compositions.

例! AI!(oH)3156g 、 85%燐酸400m/
 オ、L:び水200gから調製された燐酸水素アルミ
ニウム溶液800 gに石英800gを混合して以下A
混液と呼ぶ混合物を作った。焼成珪灰石400g 、、
未焼成珪灰石200g 、、氷状粘土500g、カリウ
ム長石150g %塩基性炭酸マグネシウム(MgC0
3−Mg(OH)−3H20)30g 、水800gオ
、fび発泡剤と泡安定剤の各0.5gを充分に混合して
以下B混液と呼ぶ混合物を作った。
example! AI! (oH) 3156g, 85% phosphoric acid 400m/
E, L: Mix 800 g of quartz with 800 g of aluminum hydrogen phosphate solution prepared from 200 g of water and prepare the following A.
I made a mixture called a mixture. 400g of calcined wollastonite,,
200 g of uncalcined wollastonite, 500 g of icy clay, 150 g of potassium feldspar, % basic magnesium carbonate (MgC0
30 g of 3-Mg(OH)-3H20), 800 g of water, and 0.5 g each of foaming agent and foam stabilizer were thoroughly mixed to prepare a mixture hereinafter referred to as mixed liquid B.

強く攪拌しつつB混液にA /f!液を注入し、1分攪
拌後混合物を鋳型に入れて成形した。20分後この成形
されたサーメットを鋳型から取出してカバーをし、24
時間室温に保った。次にこの一ソーーノット発泡体を乾
燥室内においてツo′ctroo時間乾燥し、その間に
乾燥室内の相対湿度を100ダから遂次fぽに下げた。
While stirring strongly, add A/f to the B mixture! After injecting the liquid and stirring for 1 minute, the mixture was placed in a mold and molded. After 20 minutes, the molded cermet was removed from the mold, covered, and heated for 24 minutes.
It was kept at room temperature for an hour. Next, this one-sew-knot foam was dried in a drying chamber for two hours, during which time the relative humidity in the drying chamber was gradually lowered from 100 degrees to f degrees.

最後例成形体を1260±15°Cで焼成し、焼結多孔
性成形体を得た。
The molded body of the final example was fired at 1260±15°C to obtain a sintered porous molded body.

例2 焼成珪灰石300g、未焼成珪灰石300g、、粘土5
00g。
Example 2 Calcined wollastonite 300g, uncalcined wollastonite 300g, Clay 5
00g.

カリウム長石150g、塩基性炭酸マグネシウム40g
1水850gおよび界面活性剤0.5gを充分混合して
以下C混液と呼ぶ混合物を作つit。強く攪拌しつつこ
のC混液に例1のA混液1600gを注入し、1分攪拌
後この混合物を鋳型に入れて成形した。このようにして
得られノヒサーメント成形体を鋳型から取出してカバー
を施し、室温に24時間保った。次にこの発泡サーメッ
トU形体を乾燥室内において80°Cて90時間乾燥し
、その間に乾燥室内の相対湿度を100%から遂次10
%まで下げた。最後に成形体を1240±15°Cで焼
成し、焼結多孔性成形体を街だ、。
Potassium feldspar 150g, basic magnesium carbonate 40g
1. 850 g of water and 0.5 g of surfactant are thoroughly mixed to make a mixture hereinafter referred to as C mixture. While vigorously stirring, 1600 g of mixed solution A from Example 1 was poured into the mixed solution C, and after stirring for 1 minute, the mixture was placed in a mold and molded. The thus obtained nohi sament molded body was taken out of the mold, covered, and kept at room temperature for 24 hours. Next, this foamed cermet U-shaped body was dried in a drying chamber at 80°C for 90 hours, during which time the relative humidity in the drying chamber was gradually increased from 100% to 10%.
reduced to %. Finally, the molded body is fired at 1240±15°C to produce a sintered porous molded body.

例3 焼成珪灰石1385g 、、未焼成珪灰石1115g、
、長7」’i’50g、粘度2400g 、、塩基性炭
酸マグネシウム200乙、水3750gおよび界面活性
剤58を充分混合して以下り混液と呼ぶ混合物を作つk
。強く攪拌しつつこのD混液に例1のA混液’7500
gを注入し、1分攪拌後この混合物を鋳型に入れて成形
した。20分後このようにして得られだヴーーメソト成
形イ本を鋳型から取出してカッく−を施し、室温に24
8考間イ呆った。次にこの発泡ダーーメツト成形材(を
Q乞j栗室[)」において50’C、で120時間乾燥
し、この間に乾j栗室1町の相対湿度を100%から遂
次+o%tて−Fkjだ。最後に成形体を1290±1
5°Cて焼成して敷り結多イし性)′y。
Example 3 Calcined wollastonite 1385g, Uncalcined wollastonite 1115g,
, length 7'' 50g, viscosity 2400g, basic magnesium carbonate 200g, water 3750g and surfactant 58 are thoroughly mixed to make a mixture hereinafter referred to as mixed liquid.
. While stirring strongly, add the A mixture '7500 of Example 1 to this D mixture.
After stirring for 1 minute, the mixture was put into a mold and molded. After 20 minutes, the thus obtained molded product was removed from the mold, coated, and heated to room temperature for 24 hours.
I was stunned after thinking about it. Next, this foamed dermet molded material was dried at 50'C for 120 hours in a Kurimuro laboratory, and during this time the relative humidity of the Kurimuro was successively adjusted from 100% to +o%. It's Fkj. Finally, the molded body is 1290±1
It is easy to set after baking at 5°C).

形体を得/ξ。Obtain form/ξ.

例4 A l (OH) s  + 56 g N  85 
%燐酸350m1.%”よひ: J(250gかも調製
した燐酸水素アルミニウムm〜800gに石英′700
乙を混合して以I:E混液と称する混合4勿をf′「つ
だ。珪灰石600g 、、粘土600g 、、力)ノウ
ム長石’l?:)Og、塩貼τL炭酸マグネシウム25
g1 水900gおよび発泡剤と泡安定剤各0.5gを
充分イ昆合して以下Fγ昆液と叶ふ混合物を作った。強
く攪t<+:しつつとのF r’J!液にE混液を注入
し、1分]菫指ミ後その混合物を鋳型に入れて成形した
。20分後このようにしてIj!12.ノ杉し/こヅ−
−7ノトを鋳型から収fJi してカッく−を施し、室
温に24時間保った。次にこの発泡ヴーーメソト成形体
を乾燥室内において75・Cで95時間乾燥し、この間
に乾燥室内の相対湿度を100%75・らi鉱次10%
にFげた。最後にこの成形体を1250±15°Cで焼
成して焼結多孔性成形体を得だ。
Example 4 A l (OH) s + 56 g N 85
% phosphoric acid 350ml1. %" Yohi: J (250g of prepared aluminum hydrogen phosphate m ~ 800g of quartz
Mix B and call it the I:E mixture. F' 600 g of wollastonite, 600 g of clay, 600 g of clay, 25 g of magnesium carbonate.
g1 900 g of water and 0.5 g each of a foaming agent and a foam stabilizer were sufficiently mixed together to prepare the following mixture of Fγ kombu liquid and Kofu. Stir strongly t<+: Shitsuto's F r'J! Mixture E was poured into the solution, and after stirring for 1 minute, the mixture was put into a mold and molded. 20 minutes later Ij like this! 12. Nosugishi/Kozu-
-7 pieces were collected from the mold, cut and kept at room temperature for 24 hours. Next, this foamed Voux Mesotho molded body was dried in a drying chamber at 75.C for 95 hours, during which time the relative humidity in the drying chamber was adjusted to 100%, 75.degree.
I got an F. Finally, this molded body was fired at 1250±15°C to obtain a sintered porous molded body.

この発明は上記実施例に限定されるものではなく、その
技術的範囲内で種々の改変カー可倉ヒである。
The present invention is not limited to the above embodiments, but may be modified in various ways within the technical scope thereof.

Claims (1)

【特許請求の範囲】 (1)珪酸カルシウムおよび/またはアルミン酸カルシ
ウムのような1種まだはそれ以上の塩基性態<<   
<<’  << 機物と、0 、3 = x = 3 、I = y =
 6.1=z=ioとし、好寸しくはx=l、y = 
3、z=3としだとき式xAe203・yP206.z
H20で与えられる1種まだはそれ以」二の化合物の水
溶液と、粘土寸たはカオリンと、長石と、シリカおよび
/捷たけ燐酸アルミニウムと、随意の水とを含み、硬化
前に内部に気泡を含ませた形で化学反応により多孔性成
形体として硬化させることができる組成物を使用し、こ
の様にしてできだ成形体を乾燥し最後に焼結して製造さ
れたことを特徴とする焼結多孔性セラミック成形体。 としだとき式x Ap、、05・yP、、05.zH,
、Oで与えられる1種まだはそれ以上の化合物の水溶液
と、粘土と、カリウム長石と、シリカと、随意の水と、
1種捷だはそれ以上の炭酸塩まだはAI!まだはFe等
の金属のようなガス形成添加物とを含み、化学反応によ
り硬化して多孔性成形体となるような組成物を使用し、
この様にしてできた成形体を乾燥し最後に焼結して製造
されたことを特徴とする焼結多孔性セラミック成形体。 +31 1記組成物が外部から熱の補給なく化学反応に
より硬化するようになっていることを特徴とする特許請
求の範囲(1)または(2〕記載の成形体。 (4)温度800〜1500℃、好ましくは1000〜
1300℃で焼結されたことを特徴とする特許請求の範
囲+1)、(2)または(3)記載の成形体。 (5)上記組成物がさらに界面活性剤を含むことを特徴
とする特許請求の範囲(+)、(2)、(31または(
4)記載の成形体。 (6)  珪酸カルシウムおよび7才たけアルミン酸カ
ルシウム10〜65重量%、好ましくは20〜65重量
く〈 %と、Q、3=)(=31,4y46.1工z工10、
 好ま1〜<はx=l ’t y=3 、z=3とした
とき式XAl2O5。 yP20.・z H20て与えられる1種まだはそれ以
上の5〜40重量%と、粘土寸だはカオリン5〜30重
量%と、長石1〜10重量%と、シリカおよび/捷だは
燐酸アルミニウム10〜40重量%とを含み、すべての
重量%が乾燥物で計算された組成物から製造されたこと
を特徴とする特許請求の範囲flL、 (2)、(3)
、(4)まだは(5)記載の成形体。
[Scope of Claims] (1) One or more basic forms such as calcium silicate and/or calcium aluminate <<
<<'<< Machine and 0, 3 = x = 3, I = y =
6.1=z=io, preferably x=l, y=
3. When z=3, the formula xAe203・yP206. z
It contains an aqueous solution of one or more compounds given by H20, clay or kaolin, feldspar, silica and/or precipitated aluminum phosphate, and optionally water, with air bubbles inside before curing. The invention is characterized in that it is manufactured by using a composition that can be hardened into a porous molded body through a chemical reaction in a form that contains it, and then drying the resulting molded body and finally sintering it. Sintered porous ceramic molded body. Toshidatoki formula x Ap,,05・yP,,05. zH,
, an aqueous solution of one or more compounds given by O, clay, potassium feldspar, silica, and optionally water,
If it's 1st grade, it's more carbonate than AI! a gas-forming additive such as a metal such as Fe;
A sintered porous ceramic molded article characterized in that it is produced by drying the molded article thus produced and finally sintering it. +31 The molded article according to claim (1) or (2), characterized in that the composition of item 1 is cured by a chemical reaction without external heat supply. (4) Temperature: 800-1500 °C, preferably 1000~
The molded article according to claim +1), (2) or (3), which is sintered at 1300°C. (5) Claim (+), (2), (31) or (
4) The molded article described above. (6) Calcium silicate and calcium aluminate 10-65% by weight, preferably 20-65% by weight,
Preferably 1~< is the formula XAl2O5 when x=l'ty=3 and z=3. yP20. - 5 to 40% by weight of one type given by H20 or more, 5 to 30% by weight of kaolin for clay, 1 to 10% by weight of feldspar, and 10 to 10% of aluminum phosphate for silica and/or silicate. 40% by weight, all weight% calculated on dry matter, (2), (3)
, (4) still the molded article described in (5).
JP58165836A 1982-09-08 1983-09-07 Sintered porous ceramic product Pending JPS5969461A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE82050964 1982-09-08
SE8205096A SE8205096D0 (en) 1982-09-08 1982-09-08 SINTRAD POROS CERAMIC FORM BODY

Publications (1)

Publication Number Publication Date
JPS5969461A true JPS5969461A (en) 1984-04-19

Family

ID=20347752

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58165836A Pending JPS5969461A (en) 1982-09-08 1983-09-07 Sintered porous ceramic product

Country Status (8)

Country Link
JP (1) JPS5969461A (en)
BR (1) BR8304837A (en)
DE (1) DE3331613A1 (en)
ES (1) ES8404965A1 (en)
FR (1) FR2532644A1 (en)
GB (1) GB2129416A (en)
IT (1) IT1169462B (en)
SE (2) SE8205096D0 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108585940A (en) * 2018-04-25 2018-09-28 东南大学 Phosphate porous ceramic and its preparation method and application

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4329558A1 (en) * 1993-09-02 1995-03-09 Friedrich Dr Ing Sperling Soot filter for diesel engines
FR2857961A1 (en) * 2003-07-24 2005-01-28 Centre Nat Rech Scient Preparation of a monolithic solid inorganic sponge with three degrees of porosity for a wide range of filtration and insulation applications

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1074423A (en) * 1964-09-14 1967-07-05 Horizons Inc Improvements in or relating to ceramic material
CA1186130A (en) * 1981-06-16 1985-04-30 Jeffery L. Barrall Rigid, water-resistant phosphate ceramic materials and processes for preparing them

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108585940A (en) * 2018-04-25 2018-09-28 东南大学 Phosphate porous ceramic and its preparation method and application

Also Published As

Publication number Publication date
SE8205096D0 (en) 1982-09-08
FR2532644A1 (en) 1984-03-09
ES525444A0 (en) 1984-05-16
SE8304683L (en) 1984-03-09
DE3331613A1 (en) 1984-03-08
GB8324019D0 (en) 1983-10-12
ES8404965A1 (en) 1984-05-16
SE8304683D0 (en) 1983-08-30
GB2129416A (en) 1984-05-16
BR8304837A (en) 1984-04-24
IT1169462B (en) 1987-05-27
IT8322800A0 (en) 1983-09-07
IT8322800A1 (en) 1985-03-07

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