JPS621664B2 - - Google Patents
Info
- Publication number
- JPS621664B2 JPS621664B2 JP57011980A JP1198082A JPS621664B2 JP S621664 B2 JPS621664 B2 JP S621664B2 JP 57011980 A JP57011980 A JP 57011980A JP 1198082 A JP1198082 A JP 1198082A JP S621664 B2 JPS621664 B2 JP S621664B2
- Authority
- JP
- Japan
- Prior art keywords
- mica
- hours
- inorganic binder
- heat
- mol
- 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
Links
- 239000011230 binding agent Substances 0.000 claims description 23
- KKCBUQHMOMHUOY-UHFFFAOYSA-N Na2O Inorganic materials [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 claims description 2
- 239000010445 mica Substances 0.000 description 37
- 229910052618 mica group Inorganic materials 0.000 description 37
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical group OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 8
- 235000011007 phosphoric acid Nutrition 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000003825 pressing Methods 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 235000010339 sodium tetraborate Nutrition 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 229910004844 Na2B4O7.10H2O Inorganic materials 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 229910021538 borax Inorganic materials 0.000 description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 2
- 239000004327 boric acid Substances 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- HMUNWXXNJPVALC-UHFFFAOYSA-N 1-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C(CN1CC2=C(CC1)NN=N2)=O HMUNWXXNJPVALC-UHFFFAOYSA-N 0.000 description 1
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical compound O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 150000004691 decahydrates Chemical class 0.000 description 1
- UQGFMSUEHSUPRD-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound [Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 UQGFMSUEHSUPRD-UHFFFAOYSA-N 0.000 description 1
- CDMADVZSLOHIFP-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane;decahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.[Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 CDMADVZSLOHIFP-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000033444 hydroxylation Effects 0.000 description 1
- 238000005805 hydroxylation reaction Methods 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910000403 monosodium phosphate Inorganic materials 0.000 description 1
- 235000019799 monosodium phosphate Nutrition 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 235000011008 sodium phosphates Nutrition 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B28/00—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
- C04B28/34—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing cold phosphate binders
- C04B28/342—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing cold phosphate binders the phosphate binder being present in the starting composition as a mixture of free acid and one or more reactive oxides
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Organic Chemistry (AREA)
- Laminated Bodies (AREA)
- Compositions Of Oxide Ceramics (AREA)
- Paints Or Removers (AREA)
- Adhesives Or Adhesive Processes (AREA)
Description
従来の無機のバインダーを用いたマイカ板は、
有機のバインダーを用いたマイカ板と比べて、耐
熱性を除いて耐湿性、曲げ強度、打抜き性に劣
り、更に無機特有のもろさが有り、これを補うた
めにフレークマイカ基材が使用されている。
また、ホウ酸系のバインダーを用いたマイカ板
は、有機バインダーを用いたマイカ板より高温プ
レスを必要とし、設備的にも高価となり、多大の
運転経費を必要とするため、得られるマイカ板も
高価となる。
一方、リン酸を主成分とするバインダーを用い
た場合は、前述のような高温プレスを必要とせ
ず、製造工程も簡単であるがバインダー自体が吸
湿性のため得られるマイカ板も吸湿により電気絶
縁性が著しく低下する。特に集成マイカを基材と
する場合、バインダーが重合体でないためマイカ
板の機械強度は弱く、もろさがあり、打抜き性も
劣る。
本発明は、従来のマイカ板の機械強度、打抜き
性、もろさ、耐湿性等を向上させる無機バインダ
ーを提供するものである。
本発明は、相対モル%でP2O5を20.49〜22.82,
Na2Oを31.81〜40.16,A2O3を0〜4.56および
B2O3を39.35〜40.80の範囲内で総計が100となる
ように含有してなる無機バインダーに関する。
上記の無機バインダーは、リン酸、リン酸ナト
リウム塩、リン酸アルミニウム塩、苛性ソーダ、
炭酸ソーダ、ホウ酸、ホウ酸ナトリウム等を所定
の量で配合して得られる。上記の各成分が、上記
の範囲外の場合には得られる無機バインダーが不
安定となり濁り等が生じ、耐湿性に劣る傾向があ
る。
本発明になる無機バインダーは、従来の方法に
よつてマイカ板等に適用される。上記の無機バイ
ンダーを水に溶解あるいは懸濁させて集成マイカ
シートあるいはマイカ粉に含浸させ、乾燥後、加
熱加圧して得られるマイカ板は、耐湿性、機械強
度がすぐれている。
本発明の実施例を説明する。
実施例 1
1 75%正リン酸(H3PO4)131gに無水炭酸ナト
リウム(Na2CO3)53gを添加し、更に水184g
を添加し溶解させた。次に四ホウ酸ナトリウム
10水塩(Na2B4O7・10H2O)184gを添加し、溶
解させ無機バインダーとした。
得られた無機バインダーは20.49モル%の
P2O5,40.16モル%のNa2Oおよび39.35モル%
のB2O3を含有している。
2 集成マイカシート(日立化成工業株式会社製
パルプマイカ、厚さ0.08mm500×1000mm)約70g
に上記の無機バインダーを得られるマイカシー
トに対してバインダー量を8重量%となる様に
スプレー塗布した後、105℃で30分間乾燥して
マイカシートを得た。
3 2で作成したマイカシートを20枚積層し、
190±5℃、圧力60Kgf/cm2で約2時間加熱加
圧処理し、厚さ1mmのマイカ板を得た。
4 3で得たマイカ板を開放状態で乾燥機に入れ
90℃から200℃まで約6時間かけて昇温し200℃
で4時間処理した。更にマイカ板を電気炉に入
れ200℃から650℃まで約8時間かけて昇温し
650℃で3時間加熱処理し、耐熱マイカ板を得
た。
実施例 2
1 実施例1の2で作成したマイカシートを20枚
積層し380±10℃、圧力100Kgf/cm2で約1時間
加熱加圧処理し、約1mmのマイカ板を得た。
2 1で得たマイカ板を開放状態で200℃の乾燥
器に入れ3時間処理した。更にマイカ板を電気
炉に移し200℃から650℃まで約8時間かけて昇
温し、650℃で3時間加熱処理し耐熱マイカ板
を得た。
実施例 3
1 75%正リン酸(H3PO4)65.3gに二水素リン
酸ナトリウム(NaH2PO4・2H2O)78.0gを添加
し、更に水186gを添加し溶解させ、水酸化ア
ルミニウム(A(OH)3)13.0gを添加し溶解
させた。次いで四ホウ酸ナトリウム10水塩
(Na2B4O7・10H2O)170.5gを添加して無機バ
インダーとした。
得られた無機バインダーは22.82モル%の
P2O5,31.81モル%のNa2O,4.56モル%のA
2O3および40.80モル%のB2O3を含有してい
る。
2 実施例1で用いた集成マイカシート約70g
に、上記の無機バインダーを得られるマイカシ
ートに対してバインダー量を8重量%となるよ
うにスプレー塗布した後、105℃で60分間乾燥
してマイカシートを得た。
3 2で作成したマイカシートを20枚積層し、
380±10℃、圧力100Kgf/cm2で約1時間加熱加
圧処理し、厚さ約1mmのマイカ板を得た。
4 3で得たマイカ板を開放状態で乾燥器に入れ
室温から200℃まで約6時間かけて昇温し、200
℃で3時間処理した。更にマイカ板を電気炉に
移し200℃から650℃まで約8時間かけて昇温し
650℃で3時間処理し耐熱マイカ板を得た。
表1に実施例で得た耐熱マイカ板の特性の一例
を示す。
Mica boards using conventional inorganic binders are
Compared to mica boards made with organic binders, they are inferior in moisture resistance, bending strength, and punching properties, in addition to heat resistance, and are also brittle, which is unique to inorganic materials.Flake mica base materials are used to compensate for this. . In addition, mica boards using boric acid binders require higher temperature pressing than mica boards using organic binders, are more expensive in terms of equipment, and require a large amount of operating expenses. It becomes expensive. On the other hand, when using a binder whose main component is phosphoric acid, there is no need for high-temperature pressing as mentioned above and the manufacturing process is simple, but since the binder itself is hygroscopic, the resulting mica plate also becomes electrically insulating due to moisture absorption. sex is significantly reduced. In particular, when a composite mica is used as a base material, the mechanical strength of the mica plate is low, it is brittle, and its punchability is poor because the binder is not a polymer. The present invention provides an inorganic binder that improves the mechanical strength, punchability, brittleness, moisture resistance, etc. of conventional mica plates. The present invention provides P 2 O 5 in relative mol% of 20.49 to 22.82,
Na 2 O from 31.81 to 40.16, A 2 O 3 from 0 to 4.56 and
This invention relates to an inorganic binder containing B 2 O 3 in a range of 39.35 to 40.80, with a total content of 100. The above inorganic binders include phosphoric acid, sodium phosphate, aluminum phosphate, caustic soda,
It is obtained by blending soda carbonate, boric acid, sodium borate, etc. in predetermined amounts. When each of the above components is outside the above range, the resulting inorganic binder becomes unstable, becomes cloudy, and tends to have poor moisture resistance. The inorganic binder of the present invention is applied to a mica plate or the like by a conventional method. A mica plate obtained by dissolving or suspending the above-mentioned inorganic binder in water and impregnating it into a composite mica sheet or mica powder, drying it, and then heating and pressing it has excellent moisture resistance and mechanical strength. Examples of the present invention will be described. Example 1 1 53 g of anhydrous sodium carbonate (Na 2 CO 3 ) was added to 131 g of 75% orthophosphoric acid (H 3 PO 4 ), and then 184 g of water was added.
was added and dissolved. Then sodium tetraborate
184 g of decahydrate (Na 2 B 4 O 7 .10H 2 O) was added and dissolved to form an inorganic binder. The obtained inorganic binder contained 20.49 mol%
P2O5 , 40.16 mol% Na2O and 39.35 mol%
of B 2 O 3 . 2 Laminated mica sheet (pulp mica manufactured by Hitachi Chemical Co., Ltd., thickness 0.08 mm 500 x 1000 mm) approximately 70 g
The above-mentioned inorganic binder was spray coated on the mica sheet so that the binder amount was 8% by weight, and then dried at 105° C. for 30 minutes to obtain a mica sheet. 3 Layer 20 mica sheets created in 2,
Heat and pressure treatment was carried out at 190±5° C. and a pressure of 60 Kgf/cm 2 for about 2 hours to obtain a mica plate with a thickness of 1 mm. 4 Place the mica board obtained in step 3 in the dryer in an open state.
The temperature is raised from 90℃ to 200℃ over about 6 hours and then heated to 200℃.
It was treated for 4 hours. Furthermore, the mica plate was placed in an electric furnace and heated from 200℃ to 650℃ over about 8 hours.
Heat treatment was performed at 650°C for 3 hours to obtain a heat-resistant mica board. Example 2 1 20 mica sheets prepared in Example 1-2 were laminated and subjected to heating and pressure treatment at 380±10° C. and a pressure of 100 Kgf/cm 2 for about 1 hour to obtain a mica plate of about 1 mm. 2. The mica plate obtained in 1 was placed in an open oven at 200°C and treated for 3 hours. Furthermore, the mica board was transferred to an electric furnace, and the temperature was raised from 200°C to 650°C over about 8 hours, and then heat-treated at 650°C for 3 hours to obtain a heat-resistant mica board. Example 3 1 78.0 g of sodium dihydrogen phosphate (NaH 2 PO 4 .2H 2 O) was added to 65.3 g of 75% orthophosphoric acid (H 3 PO 4 ), and 186 g of water was further added and dissolved, followed by hydroxylation. 13.0 g of aluminum (A(OH) 3 ) was added and dissolved. Next, 170.5 g of sodium tetraborate decahydrate (Na 2 B 4 O 7 .10H 2 O) was added to form an inorganic binder. The obtained inorganic binder contained 22.82 mol%
P 2 O 5 , 31.81 mol% Na 2 O, 4.56 mol% A
2 O 3 and 40.80 mol% B 2 O 3 . 2 Approximately 70g of laminated mica sheet used in Example 1
Then, the above-mentioned inorganic binder was spray-coated to the mica sheet so that the binder amount was 8% by weight, and then dried at 105° C. for 60 minutes to obtain the mica sheet. 3 Layer 20 mica sheets created in 2,
Heat and pressure treatment was carried out at 380±10° C. and a pressure of 100 Kgf/cm 2 for about 1 hour to obtain a mica plate with a thickness of about 1 mm. 4 Place the mica plate obtained in step 3 in an open dryer and raise the temperature from room temperature to 200℃ over about 6 hours.
It was treated at ℃ for 3 hours. Furthermore, the mica plate was transferred to an electric furnace and heated from 200℃ to 650℃ over about 8 hours.
A heat-resistant mica board was obtained by processing at 650°C for 3 hours. Table 1 shows an example of the characteristics of the heat-resistant mica board obtained in the example.
【表】【table】
【表】
本発明になる無機バインダーを使用することに
より曲げ強度、耐湿性等がすぐれる耐熱マイカ板
を得ることができる。[Table] By using the inorganic binder of the present invention, a heat-resistant mica board having excellent bending strength, moisture resistance, etc. can be obtained.
Claims (1)
31.81〜40.16,A2O3を0〜4.56およびB2O3を
39.35〜40.80の範囲内で総計が100となるように
含有してなる無機バインダー。1 P2O5 in relative mol% 20.49-22.82 , Na2O
31.81 ~ 40.16 , A2O3 from 0~4.56 and B2O3
An inorganic binder containing 100 in the range of 39.35 to 40.80.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57011980A JPS58130160A (en) | 1982-01-27 | 1982-01-27 | Inorganic binder |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57011980A JPS58130160A (en) | 1982-01-27 | 1982-01-27 | Inorganic binder |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS58130160A JPS58130160A (en) | 1983-08-03 |
| JPS621664B2 true JPS621664B2 (en) | 1987-01-14 |
Family
ID=11792746
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP57011980A Granted JPS58130160A (en) | 1982-01-27 | 1982-01-27 | Inorganic binder |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS58130160A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS646975U (en) * | 1987-07-02 | 1989-01-17 |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0341168Y2 (en) * | 1985-08-05 | 1991-08-29 | ||
| JP2813060B2 (en) * | 1990-11-28 | 1998-10-22 | 株式会社曙ブレーキ中央技術研究所 | Non-asbestos friction material |
| PT861216E (en) * | 1995-11-17 | 2000-11-30 | Univ Bruxelles | COMPOSITIONS OF INORGANIC RESINS, THEIR PREPARATION AND THEIR USE |
| CN112408939B (en) * | 2020-11-09 | 2022-05-13 | 湖北工业大学 | Mica plate and preparation method thereof |
-
1982
- 1982-01-27 JP JP57011980A patent/JPS58130160A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS646975U (en) * | 1987-07-02 | 1989-01-17 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS58130160A (en) | 1983-08-03 |
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