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JPH0218300B2 - - Google Patents
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JPH0218300B2 - - Google Patents

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Publication number
JPH0218300B2
JPH0218300B2 JP6451584A JP6451584A JPH0218300B2 JP H0218300 B2 JPH0218300 B2 JP H0218300B2 JP 6451584 A JP6451584 A JP 6451584A JP 6451584 A JP6451584 A JP 6451584A JP H0218300 B2 JPH0218300 B2 JP H0218300B2
Authority
JP
Japan
Prior art keywords
fibers
ceramic
ceramic fiber
molded
organic adhesive
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
Application number
JP6451584A
Other languages
Japanese (ja)
Other versions
JPS60210563A (en
Inventor
Jusaku Kobayashi
Toshimoto Yamamoto
Misao Nobori
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.)
Ibiden Co Ltd
Original Assignee
Ibiden Co 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 Ibiden Co Ltd filed Critical Ibiden Co Ltd
Priority to JP6451584A priority Critical patent/JPS60210563A/en
Publication of JPS60210563A publication Critical patent/JPS60210563A/en
Publication of JPH0218300B2 publication Critical patent/JPH0218300B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

〔産業上の利用分野〕 本発明は、炉壁の充填材或いはシール材として
用いるセラミツク繊維構造物の形成方法に関す
る。 〔従来の技術および発明が解決しようとする課
題〕 セラミツク繊維は、一般に500〜1300℃の高温
断熱材として用いられており、これを炉壁の充填
材或いはシール材として用いる場合には、セラミ
ツク繊維を圧縮した状態で炉壁等に取り付ける必
要がある。 しかしながら、セラミツク繊維を圧縮した状態
で目地等の狭い間〓全体に均一に充填することは
軟弱であるため困難であり、また充填した後の復
元性にも問題があつた。 そのため、セラミツク繊維のシート状物に熱膨
張性を付与し、加熱後に充填及びシール性、復元
性を改良する試みがいくつかなされて来た。その
一例として、特開昭49−105319号公報によれば、
セラミツク繊維を真空パツクし炉壁面等に取り付
けた後は真空パツクを除去し、該繊維の復元力で
膨張させ目地等の間〓に充填することが開示され
ている。しかしながら、この方法によれば、真空
パツクによりセラミツク繊維を一定方向に圧縮し
ているため、その形状や寸法には一定の制限があ
り、取り付ける対象物に応じ寸法を調整すること
は困難なものであつた。一方、特開昭50−55603
号公報によれば、セラミツク繊維中に加熱膨張性
のある雲母(バーミキユライト)を混入し、湿式
抄造したシート状物を熱膨張性シートとして使用
することが開示されている。しかしながら、上記
シートはバーミキユライトが1100〜1150℃で熱分
解し、熱分解したバーミキユライトがセラミツク
繊維表面と反応し熱溶融して耐熱性を失い、セラ
ミツク繊維の常用温度である1260℃以上の使用に
耐えない欠点がある。また、上記シートはいわゆ
る湿式法で成形されるため乾燥コストが必要なた
め製造コストが高くなる。 本発明は、このような従来技術の欠点を除去・
改善することを目的としてあらゆる形状の構造物
に対しても寸法精度および耐熱性に優れ、かつ容
易に製造することができるセラミツク繊維構造物
の形成方法を提供することによつて、前記目的を
達成するものである。 〔課題を解決するための手段〕 本発明のセラミツク繊維構造物の形成方法は、
加熱することにより軟化する有機系接着剤により
0.1〜0.3g/cm2の嵩密度に圧縮成形されたセラミ
ツク繊維の成形体を所定の箇所に配設した後、前
記有機系接着剤の軟化温度以上に加熱してセラミ
ツク繊維を復元させることを特徴とする。 すなわち、本発明は加熱により繊維の配列面と
は直角方向に約2倍膨張し得るセラミツク繊維成
形体を配設し、高温断熱材としてはもちろん炉壁
のスペーサーとしての充填材あるいはその他のシ
ール材としてのシール効果をも期待するセラミツ
ク繊維構造物の形成方法である。 以下、本発明のセラミツク繊維構造物の形成方
法を図面や実施例に基づいて具体的に説明する。 本発明の構造物に使用されるセラミツク繊維
は、シリカとアルミナとを主成分とする鉱物原料
を高温で加熱溶融した高温溶融体をブローイング
又はスピニング法により繊維状となし、このよう
にして得られる繊維をネツトを介して空気吸引し
集綿されることによつて層状に繊維が配列された
成形体が得られるものであつて、一般によく知ら
れているものである。この点は、従来のスペーサ
ーも同様な成形体からつくられる。 本発明によれば、前記成形体を嵩密度が0.1〜
0.3g/cm3の範囲になるように圧縮した状態で維
持させるものであり、そのためには100〜350℃の
温度範囲で軟化し流動性を有する熱可塑性樹脂を
主成分とする有機系接着剤で繊維を前記の嵩密度
となるように拘束した状態で成形しておくことが
必要である。これを図面に基づいて具体的に説明
すれば次の通りである。 第1図は、セラミツク繊維の成形体の繊維の絡
み状態を示す説明図であり、この図面において繊
維1は互いに絡み合つて各方向に散在しており、
繊維間には空〓2が存在している。この成形体を
嵩密度0.1〜0.3、最も好ましくは0.13〜0.20g/
cm3となるよう圧縮したセラミツク繊維100重量部
に対し2〜15重量部の前記有機系接着剤が含有さ
れるよう繊維表面に均一に添着させ乾燥すると、
第2図のセラミツク繊維成形体の拡大説明図のよ
うに繊維1が一定の方向に整置配列された状態と
なり、繊維間空〓2は極めて少なくなる。 そして、前記有機系接着剤による繊維の拘束状
態が解消すると第1図に示す成形体の繊維状態に
戻る。 この原理を説明すると次のようになる。まず、
成形体に使用するシート状物の繊維は嵩密度が約
0.08g/cm3であるが、これを嵩密度が0.16g/cm3
となるように体積を2分の1に圧縮し、その圧縮
状態で各温度で加熱し解消して成形体の繊維の復
元率を測つた結果を第1表に示す。
[Industrial Application Field] The present invention relates to a method for forming a ceramic fiber structure used as a filling material or a sealing material for a furnace wall. [Prior art and problems to be solved by the invention] Ceramic fibers are generally used as high-temperature insulation materials at temperatures of 500 to 1300°C. It is necessary to attach it to the furnace wall etc. in a compressed state. However, it is difficult to uniformly fill the entire narrow spaces such as joints in a compressed state because the ceramic fibers are soft and weak, and there are also problems with the resilience after filling. Therefore, several attempts have been made to impart thermal expandability to ceramic fiber sheets to improve filling, sealing, and restoring properties after heating. As an example, according to Japanese Patent Application Laid-open No. 105319/1983,
It is disclosed that after vacuum packing ceramic fibers and attaching them to a furnace wall surface, etc., the vacuum packing is removed, and the fibers are expanded by the restoring force and filled between joints and the like. However, according to this method, the ceramic fibers are compressed in a certain direction using a vacuum pack, so there are certain restrictions on the shape and dimensions, and it is difficult to adjust the dimensions depending on the object to be attached. It was hot. On the other hand, JP-A-50-55603
According to the publication, it is disclosed that heat-expandable mica (vermiculite) is mixed into ceramic fibers, and a wet paper-formed sheet is used as a heat-expandable sheet. However, in the above sheet, vermiculite thermally decomposes at 1100 to 1150°C, and the thermally decomposed vermiculite reacts with the surface of the ceramic fiber and melts, losing heat resistance, and the temperature exceeds 1260°C, which is the normal temperature of ceramic fiber. There are drawbacks that make it unusable. Furthermore, since the sheet is molded by a so-called wet method, drying costs are required, which increases manufacturing costs. The present invention eliminates and eliminates such drawbacks of the prior art.
The above object is achieved by providing a method for forming a ceramic fiber structure that has excellent dimensional accuracy and heat resistance and can be easily manufactured for structures of any shape. It is something to do. [Means for Solving the Problems] The method for forming a ceramic fiber structure of the present invention includes:
With organic adhesive that softens when heated
After arranging a molded body of ceramic fiber compression molded to a bulk density of 0.1 to 0.3 g/cm 2 at a predetermined location, the ceramic fiber is restored by heating to a temperature higher than the softening temperature of the organic adhesive. Features. That is, the present invention provides a ceramic fiber molded body that can expand approximately twice as much when heated in a direction perpendicular to the fiber arrangement plane, and can be used not only as a high-temperature insulating material but also as a filler or other sealing material as a spacer for the furnace wall. This is a method of forming a ceramic fiber structure that is expected to have a sealing effect as well. Hereinafter, the method for forming the ceramic fiber structure of the present invention will be specifically explained based on drawings and examples. The ceramic fiber used in the structure of the present invention is obtained by heating and melting a mineral raw material mainly composed of silica and alumina at high temperature to form a fibrous material by blowing or spinning. This is a generally well-known method in which a molded article in which fibers are arranged in layers is obtained by collecting the fibers by suctioning air through a net. In this respect, conventional spacers are also made from a similar molded body. According to the present invention, the molded body has a bulk density of 0.1 to
It is maintained in a compressed state in the range of 0.3g/ cm3 , and for this purpose an organic adhesive whose main component is a thermoplastic resin that softens and has fluidity in the temperature range of 100 to 350℃. It is necessary to mold the fibers in a restrained state so that they have the above-mentioned bulk density. This will be specifically explained based on the drawings as follows. FIG. 1 is an explanatory diagram showing the state of entanglement of fibers in a ceramic fiber molded body. In this figure, fibers 1 are intertwined with each other and scattered in each direction.
There is a void 〓2 between the fibers. This molded body has a bulk density of 0.1 to 0.3, most preferably 0.13 to 0.20 g/
When 2 to 15 parts by weight of the organic adhesive is uniformly applied to the surface of the fibers and dried, 100 parts by weight of ceramic fibers compressed to a volume of 100 cm 3 are obtained.
As shown in the enlarged explanatory view of the ceramic fiber molded article in FIG. 2, the fibers 1 are arranged in a fixed direction, and the inter-fiber spaces 2 are extremely small. When the fibers are no longer restrained by the organic adhesive, they return to the fiber state of the molded article shown in FIG. This principle can be explained as follows. first,
The bulk density of the fibers used in the sheet material used in the molded product is approximately
0.08g/cm 3 , but the bulk density is 0.16g/cm 3
Table 1 shows the results of measuring the recovery rate of the fibers of the molded product by compressing the volume to one-half so that the compressed state was heated at various temperatures to dissolve the molded product.

【表】 第1表からも明らかなように、第1図の成形体
の繊維の体積を2分の1に圧縮したときの復元率
は、200〜300℃の範囲が2倍強で最も大きく、
400℃以上になると小さくなる。そのため100〜
350℃で加熱軟化し繊維の拘束力を失う有機系接
着剤を使用することが最適であることを新規に知
見した。この知見に基づいて成形体がつくられる
ものであるがそのために具備すべき必要な条件
は、次の通りである。第1の条件としては成形体
のセラミツク繊維が層状に積層され、しかも繊維
長の平均値が50mm以上であることが必要である。
その理由は、繊維の平均値長さが50mm以下の場合
には嵩密度は大きくなるため繊維間の空気層は少
なくなり復元による膨張率は小さくなるので不適
当な繊維状態となるからである。第2の条件とし
ては積層されたセラミツク繊維が100〜350℃の温
度範囲で軟化し流動性を呈する熱可塑性樹脂を主
成分とする有機系接着剤を繊維表面に均一に添着
させて成形体の嵩密度が0.1〜0.3g/cm3となるよ
うに繊維を拘束状態とすることが必要である。そ
の理由は嵩密度が0.1g/cm3以下であると第1図
に示す繊維状態に近いものとなり、加熱しても復
元性を呈しない。 一方、嵩密度が0.3g/cm3以上になると繊維が
折れた状態となると共に、これらの繊維は加熱し
ても何ら膨張能力を有しないものとなるからであ
る。 このように本発明によれば前記成形体は、加熱
処理温度が350℃に達すると、繊維を拘束してい
る有機系接着剤が軟化し流動性を呈する状態とな
り、繊維の拘束状態が解消され第1図に示すよう
な繊維状態となるため拘束された繊維に比較して
セラミツク繊維の層状配列面に垂直な方向に約
2.2倍膨張することになる。このように前記成形
体はセラミツク繊維の層状配列面に垂直な方向に
加熱膨張するので、セラミツク繊維の層状単体ブ
ロツクの目地等の間〓にスペーサーとして熱膨張
により目地が閉じる状態で使用すれば、従来の膨
張性雲母含有の成形体のようにすべての方向に加
熱膨張するのとは異なり目地間〓に充填挿設する
スペーサーとして最適のものである。 一方、本発明によれば前記成形体において、前
記有機系接着剤の含有量は、セラミツク繊維100
重量部に対し2〜15重量部であることが好適であ
る。その理由は、2重量部以下の含有量であると
有機系接着剤による繊維の拘束状態は得られず、
第2図の繊維状態とはならないのに対し、15重量
部を越えるとセラミツク繊維の加熱による成形体
の膨張が阻害されるからである。このようなこと
を考慮すると有機系接着剤の含有量はセラミツク
繊維100重量部に対し4〜8重量部であることが
最適な条件であり、成形体の嵩密度が0.13〜0.20
g/cm3となるように繊維を拘束して第2図に示す
繊維状態とすることが肝要である。 以下、本発明の実施例について具体的に説明す
る。 実施例 1 集綿し層状に積層したセラミツク繊維のバルク
に、最低造膜温度が8℃のSBRラテツクスエマ
ルジヨン10wt%濃度水溶液を含浸し真空吸引に
より成形し、またセラミツク繊維に対して含液率
を0.55倍まで脱水し乾燥することにより成形体を
得た。この成形体の特性は第2表に示すようなも
のであつた。
[Table] As is clear from Table 1, the recovery rate when the volume of the fibers of the molded body shown in Figure 1 is compressed to half is the highest in the range of 200 to 300℃, which is more than double. ,
It becomes smaller when the temperature exceeds 400℃. Therefore 100~
We newly discovered that it is optimal to use an organic adhesive that softens when heated at 350℃ and loses its binding force on the fibers. A molded article can be produced based on this knowledge, and the necessary conditions for this purpose are as follows. The first condition is that the ceramic fibers of the molded body are laminated in layers and that the average length of the fibers is 50 mm or more.
The reason for this is that when the average length of the fibers is 50 mm or less, the bulk density increases, the air space between the fibers decreases, and the expansion rate due to restoration decreases, resulting in an inappropriate fiber state. The second condition is that the laminated ceramic fibers are uniformly applied to the fiber surface with an organic adhesive whose main component is a thermoplastic resin that softens and exhibits fluidity in the temperature range of 100 to 350°C. It is necessary to constrain the fibers so that the bulk density is 0.1 to 0.3 g/cm 3 . The reason for this is that if the bulk density is 0.1 g/cm 3 or less, the fiber state will be similar to that shown in FIG. 1, and it will not exhibit restorability even when heated. On the other hand, if the bulk density is 0.3 g/cm 3 or more, the fibers will be in a broken state and will not have any expansion ability even when heated. As described above, according to the present invention, when the heat treatment temperature of the molded article reaches 350°C, the organic adhesive that binds the fibers softens and becomes fluid, and the restrained state of the fibers is released. As shown in Figure 1, the ceramic fibers are in a fibrous state, so compared to the restrained fibers, the ceramic fibers are in a fibrous state in a direction perpendicular to the layered arrangement plane.
It will expand 2.2 times. In this way, the molded body expands by heating in the direction perpendicular to the layered arrangement plane of the ceramic fibers, so if it is used as a spacer between the joints of a layered single block of ceramic fibers with the joints closed by thermal expansion, Unlike conventional expansible mica-containing molded products, which expand in all directions when heated, this product is ideal as a spacer to be inserted between joints. On the other hand, according to the present invention, in the molded article, the content of the organic adhesive is 100% of the ceramic fiber.
The amount is preferably 2 to 15 parts by weight. The reason is that if the content is less than 2 parts by weight, the fibers cannot be restrained by the organic adhesive.
This is because, while the fibrous state shown in FIG. 2 will not occur, if the amount exceeds 15 parts by weight, the expansion of the molded product due to heating of the ceramic fibers will be inhibited. Taking these things into consideration, the optimal condition is that the content of the organic adhesive is 4 to 8 parts by weight per 100 parts by weight of ceramic fiber, and the bulk density of the molded product is 0.13 to 0.20.
It is important to restrain the fibers so as to obtain the fiber state shown in FIG . Examples of the present invention will be specifically described below. Example 1 A bulk of ceramic fibers collected and laminated in layers was impregnated with a 10wt% aqueous solution of SBR latex emulsion with a minimum film forming temperature of 8°C, and formed by vacuum suction, and the ceramic fibers were impregnated with the liquid. A molded body was obtained by dehydration and drying to a ratio of 0.55 times. The properties of this molded body were as shown in Table 2.

【表】 得られた成形体を1000℃の炉の炉壁の目地に充
填しスペーサーとして使用したところ常用におい
てシール材としての断熱性およびシール性が充分
発揮され炉の熱効率および耐久性が向上した。 実施例 2 ブローイング法で繊維化する際に最低造膜温度
45℃の5wt%濃度アクリル樹脂エマルジヨン水溶
液を、出湯量に対して同一重量分吹き付け、繊維
に均一に添着させ、セラミツク繊維に対して0.5
〜10wt%程度含水した状態で層状に積層したセ
ラミツクフアイバーのバルクを、層を圧縮した状
態でプレスし、そのまま乾燥して成形体を得た。
この際吹き付け液量がすくないために推積した時
点で全く含水していなければ、樹脂による接着効
果がなくなるため不可である。この時の成形体の
特性は第3表に示すようなものとなつた。
[Table] When the obtained compact was filled into the joints of the furnace wall of a 1000°C furnace and used as a spacer, it exhibited sufficient heat insulation and sealing properties as a sealing material during regular use, improving the thermal efficiency and durability of the furnace. . Example 2 Minimum film forming temperature when fiberizing by blowing method
Spray an aqueous solution of 5 wt% acrylic resin emulsion at 45℃ in the same weight amount based on the amount of hot water released, and apply it uniformly to the fibers.
A bulk of ceramic fibers laminated in layers with a water content of about 10 wt% was pressed while the layers were compressed, and dried as it was to obtain a molded body.
In this case, since the amount of sprayed liquid is so small that it does not contain any water at the time of estimation, it is impossible to do so because the adhesive effect of the resin will be lost. The properties of the molded product at this time were as shown in Table 3.

〔発明の効果〕〔Effect of the invention〕

上記の如く本発明のセラミツク繊維構造物の形
成方法はブランケツト、フエルト等の一般の乾式
セラミツク繊維シート状物と同程度に安価に製造
でき、加工が容易な圧縮成形されたセラミツク繊
維の成形体を配設しその後加熱により復元させた
のであるから高温で使用する耐熱性のシール材、
充填材の形成方法として最適であり、産業上有用
である。
As described above, the method for forming the ceramic fiber structure of the present invention can produce a compression-molded ceramic fiber compact that is as inexpensive as general dry ceramic fiber sheets such as blankets and felts, and is easy to process. Because it was installed and then restored by heating, it is a heat-resistant sealing material that can be used at high temperatures.
This is an optimal method for forming fillers and is industrially useful.

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

第1図は、従来セラミツク繊維の成形体の繊維
状態を示す説明図、第2図は本発明による熱膨張
性セラミツク繊維成形体の繊維配列状態を示す拡
大説明図である。 図面において、1はセラミツク繊維、2は繊維
間空〓である。
FIG. 1 is an explanatory view showing the fiber state of a conventional ceramic fiber molded article, and FIG. 2 is an enlarged explanatory diagram showing the fiber arrangement state of a thermally expandable ceramic fiber molded article according to the present invention. In the drawings, 1 is a ceramic fiber and 2 is a space between the fibers.

Claims (1)

【特許請求の範囲】 1 加熱することにより軟化する有機系接着剤に
より0.1〜0.3g/cm2の嵩密度に圧縮成形されたセ
ラミツク繊維の成形体を所定の箇所に配設した
後、前記有機系接着剤の軟化温度以上に加熱して
セラミツク繊維を復元させることを特徴とすセラ
ミツク繊維構造物の形成方法。 2 前記有機系接着剤の軟化温度は、100〜350℃
の範囲である特許請求の範囲第1項記載のセラミ
ツク繊維構造物の形成方法。 3 前記有機系接着剤はセラミツク繊維100重量
部に対し2〜15重量部含有され、前記繊維に均一
に添着されている特許請求の範囲第1項記載のセ
ラミツク繊維構造物の形成方法。
[Scope of Claims] 1. After arranging at a predetermined location a ceramic fiber molded body compression-molded to a bulk density of 0.1 to 0.3 g/cm 2 using an organic adhesive that softens when heated, A method for forming a ceramic fiber structure, which comprises restoring ceramic fibers by heating the adhesive to a temperature higher than the softening temperature of the adhesive. 2 The softening temperature of the organic adhesive is 100 to 350°C.
A method for forming a ceramic fiber structure according to claim 1, which falls within the scope of claim 1. 3. The method of forming a ceramic fiber structure according to claim 1, wherein the organic adhesive is contained in an amount of 2 to 15 parts by weight per 100 parts by weight of the ceramic fibers and is uniformly attached to the fibers.
JP6451584A 1984-03-31 1984-03-31 Thermally expansive ceramic fiber formed body Granted JPS60210563A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6451584A JPS60210563A (en) 1984-03-31 1984-03-31 Thermally expansive ceramic fiber formed body

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6451584A JPS60210563A (en) 1984-03-31 1984-03-31 Thermally expansive ceramic fiber formed body

Publications (2)

Publication Number Publication Date
JPS60210563A JPS60210563A (en) 1985-10-23
JPH0218300B2 true JPH0218300B2 (en) 1990-04-25

Family

ID=13260421

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6451584A Granted JPS60210563A (en) 1984-03-31 1984-03-31 Thermally expansive ceramic fiber formed body

Country Status (1)

Country Link
JP (1) JPS60210563A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005118467A1 (en) * 2004-06-02 2005-12-15 Ebara Ballard Corporation Fuel treating device
JP2022503876A (en) * 2018-09-28 2022-01-12 トレンコ シーピージー ユーケー リミテッド Flame stop product

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2603974B2 (en) * 1987-12-03 1997-04-23 浩章 堀津 Porous ceramic sintered body and method for producing the same

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005118467A1 (en) * 2004-06-02 2005-12-15 Ebara Ballard Corporation Fuel treating device
JP2022503876A (en) * 2018-09-28 2022-01-12 トレンコ シーピージー ユーケー リミテッド Flame stop product

Also Published As

Publication number Publication date
JPS60210563A (en) 1985-10-23

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