JPS63182499A - Production of non-asbestos type beater sheet - Google Patents
Production of non-asbestos type beater sheetInfo
- Publication number
- JPS63182499A JPS63182499A JP1156487A JP1156487A JPS63182499A JP S63182499 A JPS63182499 A JP S63182499A JP 1156487 A JP1156487 A JP 1156487A JP 1156487 A JP1156487 A JP 1156487A JP S63182499 A JPS63182499 A JP S63182499A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- parts
- asbestos
- fibers
- sheet
- 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
Links
- 239000010425 asbestos Substances 0.000 title claims description 22
- 229910052895 riebeckite Inorganic materials 0.000 title claims description 22
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 229920003043 Cellulose fiber Polymers 0.000 claims description 15
- 239000012210 heat-resistant fiber Substances 0.000 claims description 11
- 229920000620 organic polymer Polymers 0.000 claims description 10
- 239000011256 inorganic filler Substances 0.000 claims description 9
- 229910003475 inorganic filler Inorganic materials 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 7
- 239000002491 polymer binding agent Substances 0.000 claims description 7
- 239000012784 inorganic fiber Substances 0.000 claims description 5
- 239000006185 dispersion Substances 0.000 claims description 3
- 239000000835 fiber Substances 0.000 description 30
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 239000000919 ceramic Substances 0.000 description 7
- 229920000800 acrylic rubber Polymers 0.000 description 6
- 239000011490 mineral wool Substances 0.000 description 6
- 229920000058 polyacrylate Polymers 0.000 description 6
- 238000007789 sealing Methods 0.000 description 6
- 239000004927 clay Substances 0.000 description 5
- 238000004132 cross linking Methods 0.000 description 5
- 239000000839 emulsion Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 229920000561 Twaron Polymers 0.000 description 2
- 239000010439 graphite Substances 0.000 description 2
- 229910002804 graphite Inorganic materials 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 239000004762 twaron Substances 0.000 description 2
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- DEXFNLNNUZKHNO-UHFFFAOYSA-N 6-[3-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperidin-1-yl]-3-oxopropyl]-3H-1,3-benzoxazol-2-one Chemical group C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1CCN(CC1)C(CCC1=CC2=C(NC(O2)=O)C=C1)=O DEXFNLNNUZKHNO-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 229920000271 Kevlar® Polymers 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- -1 Seviolite) Substances 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 238000010009 beating Methods 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- 235000012241 calcium silicate Nutrition 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 229920001973 fluoroelastomer Polymers 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000004761 kevlar Substances 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 229910052919 magnesium silicate Inorganic materials 0.000 description 1
- 235000019792 magnesium silicate Nutrition 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000010455 vermiculite Substances 0.000 description 1
- 229910052902 vermiculite Inorganic materials 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
- 239000010456 wollastonite Substances 0.000 description 1
- 229910052882 wollastonite Inorganic materials 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Landscapes
- Paper (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】
皮呈上食肌片分団
本発明は、ビータ−シートの製造方法に関し、詳しくは
自動車エンジン用あるいはその他一般産業用の各種ガス
ケット材として、特に自動車エンジンのシリンダーヘッ
ド用のガスケット材として好適な非アスベスト系ビータ
−シートの製造方法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing beater sheets, specifically for use as various gasket materials for automobile engines or other general industries, particularly for cylinder heads of automobile engines. The present invention relates to a method of manufacturing a non-asbestos beater sheet suitable as a gasket material.
の ′、並びに勺を べ 。 占
ビーターシートガスケットは、大量生産が可能であるた
めに一般に安価であり、しかも従来使用のアスベスト系
ビータ−シートガスケットはアスベストの特性が反映し
て満足すべき性能を有するため、過去において各種用途
に長年の使用実績を誇っていたが、近時における健康上
からのアスベスト排斥気運から非アスベスト系ビータ−
シートの開発が重要課題としてクローズアンプされてい
る。Be sure to read the ′′, as well as the ′′”. Since beater sheet gaskets can be mass-produced, they are generally inexpensive, and conventionally used asbestos-based beater sheet gaskets have satisfactory performance reflecting the characteristics of asbestos, so they have been used for various purposes in the past. Although it boasted a long history of use, due to the recent movement to ban asbestos from health concerns, non-asbestos beaters have been introduced.
Seat development has been highlighted as an important issue.
アスベストに代わってセラミック繊維などの非アスベス
ト系繊維を用いたビータ−シートガスケットの製造検討
が関係者の間で鋭意進められているが、未だ充分な性能
を示すものが得られていない実情にある。Stakeholders are actively investigating the manufacture of beater sheet gaskets using non-asbestos fibers such as ceramic fibers in place of asbestos, but the reality is that no product with sufficient performance has yet been obtained. .
−占”°の 並びに
本発明は、上記した実情を考慮して行った研究の成果に
基づいて完成したものであって、その要旨とするところ
は、セルロース繊維0.5〜10重量部、非アスベスト
系耐熱性繊維10〜50重置部、有機高分子結合剤2〜
15重景部垂蓋よび無機充填剤30〜90重量部からな
る成分比組成物の水分散液を抄造することを特徴とする
非アスベスト系ビータ−シートの製造方法である。The present invention was completed based on the results of research conducted in consideration of the above-mentioned circumstances, and its gist is that 0.5 to 10 parts by weight of cellulose fiber, 10 to 50 overlapping parts of asbestos-based heat-resistant fibers, 2 to 2 organic polymer binders
This is a method for producing a non-asbestos beater sheet, which is characterized by forming an aqueous dispersion of a component ratio composition consisting of 15 parts by weight and 30 to 90 parts by weight of an inorganic filler.
本発明者らの研究から、繊維材料とてセルロース繊維と
非アスベスト系の耐熱性繊維とを特定量比で使用し、か
つこれら繊維混合物と上記特定量の有機高分子結合およ
び無機充填剤とからなる組成物の水分散液を用いて抄造
することにより、耐熱性、水シール性、並びに応力緩和
性の優れたビータ−シートが安価に得られることがわか
った。From the research of the present inventors, it has been found that the fiber material uses cellulose fibers and non-asbestos heat-resistant fibers in a specific ratio, and that a mixture of these fibers and the above-mentioned specific amounts of organic polymer bonds and inorganic fillers are used. It has been found that beater sheets with excellent heat resistance, water sealing properties, and stress relaxation properties can be obtained at low cost by paper-making using an aqueous dispersion of the composition.
大嵐炭
セルロース繊維としては、たとえば木材、麻、リング−
などの植物を細断、蒸解、叩解などの工程を経て得た種
々のものを用いることができる。Dairantan cellulose fibers include wood, hemp, ring fibers, etc.
Various plants obtained by shredding, cooking, beating, etc. can be used.
本発明においては、抄造により目的物を製造するので、
セルロース繊維はセルロースパルプの形態で使用するの
が実際的であり、亜硫酸パルプ、硫酸パルプ、ソーダパ
ルプ、塩素パルプなどを用いるのが好ましく、特に機械
強度の高い硫酸パルプが好ましい。In the present invention, since the target product is manufactured by papermaking,
It is practical to use the cellulose fiber in the form of cellulose pulp, and it is preferable to use sulfite pulp, sulfuric acid pulp, soda pulp, chlorine pulp, etc., and sulfuric acid pulp, which has high mechanical strength, is particularly preferable.
非アスベスト系の耐熱性繊維としては、ロックウール、
セラミック繊維、アルミナ繊維、シリカ繊維、表面処理
されたセラミック繊維(商品名イノ−フィルなど)、ガ
ラス繊維、天然無機繊維(セビオライトなど)などの耐
熱性無機繊維、芳香族ポリアミド繊維(商品名ケブラー
、トワロンなど)、フェノール樹脂繊維(商品名カイノ
ール)などの耐熱性有機繊維が用いられる。耐熱性無機
繊維と耐熱性有機繊維とは、それらを混合使用してもよ
い。耐熱性繊維の太さは0.3〜100μ鋼程度、好ま
しくは1〜30μm程度であり、長さは1〜501程度
、好ましくは2〜1ore程度である。上記した非アス
ベスト系耐熱性繊維のうちでは、耐熱性無機繊維、特に
ロックウール、セラミック繊維が好ましい。Non-asbestos heat-resistant fibers include rock wool,
Heat-resistant inorganic fibers such as ceramic fibers, alumina fibers, silica fibers, surface-treated ceramic fibers (product names such as Innofil), glass fibers, natural inorganic fibers (such as Seviolite), aromatic polyamide fibers (product names such as Kevlar, Heat-resistant organic fibers such as Twaron (Twaron, etc.) and phenolic resin fibers (trade name: Kynol) are used. The heat-resistant inorganic fibers and the heat-resistant organic fibers may be used in combination. The thickness of the heat-resistant fiber is about 0.3 to 100 μm, preferably about 1 to 30 μm, and the length is about 1 to 501, preferably about 2 to 1 ore. Among the non-asbestos heat-resistant fibers mentioned above, heat-resistant inorganic fibers, particularly rock wool and ceramic fibers, are preferred.
有機高分子結合剤としては、各種有機高分子のラテック
スが用いられ、この有機高分子としてはたとえばフッ素
ゴム、アクリロニトリル−ブタジェンゴム、アクリルゴ
ム、スチレン−ブタジェンゴムなどのゴム類を挙げるこ
とができる。As the organic polymer binder, latexes of various organic polymers are used, and examples of the organic polymer include rubbers such as fluororubber, acrylonitrile-butadiene rubber, acrylic rubber, and styrene-butadiene rubber.
無機充填剤としては、タルク、クレー、グラファイト、
カオリン、けい酸マグネシウム、けい酸カルシウム、バ
ーミキユライト、けいそう土・ウオラストナイト、ゼオ
ライト、セとオライド、膨張黒鉛などが用いられる。Inorganic fillers include talc, clay, graphite,
Kaolin, magnesium silicate, calcium silicate, vermiculite, diatomaceous earth/wollastonite, zeolite, ceolide, expanded graphite, etc. are used.
本発明においては、上記したセルロース繊維、非アスベ
スト系耐熱性繊維、有機高分子結合剤、および無機充填
剤は、下記の量比で混合使用される。In the present invention, the cellulose fibers, non-asbestos heat-resistant fibers, organic polymer binders, and inorganic fillers described above are mixed and used in the following quantitative ratios.
セルロース繊維:0.5〜10重量部、好ましくは3〜
7重量部(セルロース繊維としてパルプを使用する場合
には、セルロース繊維の乾燥重量に対応するパルフ量が
用いられる。)、
非アスベスト系耐熱性繊維:10〜50重量部、好まし
くは20〜40重量部、
有機高分子結合剤(ラテックス中の固形分量として):
2〜15重量部、好ましくは3〜IO重量部、
無機充填剤;30〜90重量部、好ましくは50〜70
重量部。Cellulose fiber: 0.5 to 10 parts by weight, preferably 3 to 10 parts by weight
7 parts by weight (when pulp is used as the cellulose fiber, the amount of pulp corresponding to the dry weight of the cellulose fiber is used), non-asbestos heat-resistant fiber: 10 to 50 parts by weight, preferably 20 to 40 parts by weight Part, organic polymeric binder (as solid content in latex):
2 to 15 parts by weight, preferably 3 to IO parts by weight, inorganic filler; 30 to 90 parts by weight, preferably 50 to 70 parts by weight
Weight part.
セルロース繊維の使用量が0.5重量部より少くないと
シートの抄造性が悪くなり、一方10重量部より多いと
耐熱性がかなり悪くなる。非アスベスト系耐熱性繊維の
使用量が10重量部より少くないと高温度での弾性が乏
しくなり、一方50重量部より多いと水シール性が悪く
なる。有機高分子結合剤の使用量が2重量部より少くな
いと水シール性が悪くなり、一方15垂蓋部より多いと
応力緩和性が悪くなる。また無機充填剤の使用量が30
重量部より少くないと水シール性が悪くなり、一方90
重量部より多いと弾性が悪くなる。If the amount of cellulose fiber used is less than 0.5 parts by weight, the sheet formability will be poor, while if it is more than 10 parts by weight, the heat resistance will be considerably poor. If the amount of non-asbestos heat-resistant fiber used is less than 10 parts by weight, elasticity at high temperatures will be poor, while if it is more than 50 parts by weight, water sealing properties will be poor. If the amount of the organic polymer binder used is less than 2 parts by weight, water sealing properties will be poor, while if it is more than 15 parts by weight, stress relaxation properties will be poor. In addition, the amount of inorganic filler used is 30
If it is less than 90 parts by weight, the water sealing property will be poor;
If the amount is more than parts by weight, the elasticity will deteriorate.
本発明の目的物は、セルロース繊維、非アスベスト系耐
熱性繊維、有機高分子結合剤、無機充填剤、および必要
に応じて添加されるその他の薬剤たとえば有機高分子結
合剤用の老化防止剤、加硫剤、あるいはその他ビーター
シートに通常用いられるもの、を水に分散させて長網式
抄紙機や丸網式抄紙機などによる通常の抄紙法により抄
造し、ついで抄造シートを乾燥することにより製造する
ことができる。The objects of the present invention are cellulose fibers, non-asbestos heat-resistant fibers, organic polymer binders, inorganic fillers, and other agents added as necessary, such as anti-aging agents for organic polymer binders, Manufactured by dispersing a vulcanizing agent or other materials commonly used in beater sheets in water, making paper using a normal paper making method such as a fourdrinier paper machine or a circular wire paper machine, and then drying the paper sheet. can do.
■
本発明の方法により製造されたシートは非アスベスト系
のものでありながら、安価でかつ性能的には耐熱性、水
シール性、並びに応力緩和性に優れており、従来のアス
ベスト系ビータ−シートに匹敵するシール性能を示す。■ Although the sheet manufactured by the method of the present invention is non-asbestos-based, it is inexpensive and has excellent heat resistance, water sealing properties, and stress relaxation properties, and is superior to conventional asbestos-based beater sheets. Shows sealing performance comparable to that of
したがってそのシートは、自動車エンジン用あるいはそ
の他一般産業用の各種ガスケット材として、特に自動車
エンジンのシリンダーヘッド用のガスケット材として好
適に使用することができる。Therefore, the sheet can be suitably used as various gasket materials for automobile engines or other general industries, particularly as gasket materials for cylinder heads of automobile engines.
以下、実施例および比較例により本発明を一層詳細に説
明する。Hereinafter, the present invention will be explained in more detail with reference to Examples and Comparative Examples.
実施例1
セルロース繊維5重量部、ロックウール(平均繊維径5
μm、平均繊維長5tm)15重量部、セラミック繊維
(平均繊維径2μm、平均繊維長Low)15重量部、
クレー(300sesh通過品)62重量部、アクリル
ゴム(自己架橋型アクリル酸エステル共重合体エマルジ
ッン)8重量部より。Example 1 5 parts by weight of cellulose fiber, rock wool (average fiber diameter 5
μm, average fiber length 5tm) 15 parts by weight, ceramic fiber (average fiber diameter 2 μm, average fiber length Low) 15 parts by weight,
From 62 parts by weight of clay (product that passed 300 sesh) and 8 parts by weight of acrylic rubber (self-crosslinking acrylic acid ester copolymer emulsion).
なる組成物を用いて長網式抄紙機により通常の抄紙法で
0.8龍厚のシートを得た。このシートを0.25■■
厚のフック立て鉄板の両側に貼り合わせ、1.25m■
厚のシートを作成し、このシートをシリコンレジンで含
浸加熱処理してガスケット用シートを得た。A sheet having a thickness of 0.8 mm was obtained using a fourdrinier paper machine using a conventional paper making method. This sheet is 0.25■■
Pasted on both sides of a thick hook stand iron plate, 1.25m■
A thick sheet was prepared, and this sheet was impregnated with silicone resin and heat-treated to obtain a gasket sheet.
実施例2
セルロース繊維5重量部、ロックウール(平均繊維径5
μM、平均繊維長5n+)30重量部、クレー(300
mesh通過品)62重量部、アクリルゴム(自己架橋
型アクリル酸エステル共重合体エマルジョン)8重量部
よりなる組成物を用いた以外は実施例1と同様にしてガ
スケット用シートを得た。Example 2 5 parts by weight of cellulose fiber, rock wool (average fiber diameter 5
μM, average fiber length 5n+) 30 parts by weight, clay (300
A gasket sheet was obtained in the same manner as in Example 1, except that a composition consisting of 62 parts by weight of acrylic rubber (self-crosslinking acrylic ester copolymer emulsion) and 8 parts by weight of acrylic rubber (self-crosslinking acrylic ester copolymer emulsion) was used.
実施例3
セルロース繊維5重量部、ロックウール(平均繊維径5
μm、平均繊維長5w)15重量部、セラミック繊維(
平均繊維径2μm、平均繊維長108m)15重量部、
クレー(300mesh通過品)42重量部、タルク(
300meshiil過品)20重量部、アクリルゴム
(自己架橋型アクリル酸エステ7L4i11合体エマル
ジョン)8重量部よりなる組成物を用いた以外は実施例
1と同様にしてガスケット用シートを得た。Example 3 5 parts by weight of cellulose fiber, rock wool (average fiber diameter 5
μm, average fiber length 5w) 15 parts by weight, ceramic fiber (
average fiber diameter 2 μm, average fiber length 108 m) 15 parts by weight,
42 parts by weight of clay (product passing through 300 mesh), talc (
A gasket sheet was obtained in the same manner as in Example 1, except that a composition consisting of 20 parts by weight of acrylic rubber (self-crosslinking type acrylic acid ester 7L4i11 combined emulsion) was used.
比較例1
セルロース繊維15重量部、ロックウール(平均繊維径
5μ麟、平均繊維長5fl)25重量部、セラミック繊
維(平均繊維径2μ鋼、平均繊維長ioms)25@量
部、クレー(3Q O+aeshA過品)25重量部、
アクリルゴム(自己架橋型アクリル酸エステル共重合体
エマルジョン)8重量部よりなる組成物を用いた以外は
実施例1と同様にしてガスケット用シートを得た。Comparative Example 1 15 parts by weight of cellulose fiber, 25 parts by weight of rock wool (average fiber diameter 5μ, average fiber length 5fl), 25 parts by weight of ceramic fiber (average fiber diameter 2μ steel, average fiber length ioms), clay (3Q O+AeshA) 25 parts by weight,
A gasket sheet was obtained in the same manner as in Example 1, except that a composition consisting of 8 parts by weight of acrylic rubber (self-crosslinking acrylic ester copolymer emulsion) was used.
実施例1〜3、比較例1で得たガスゲット用シートにつ
き下記試験を行い、その結果を表に示した。The following tests were conducted on the gas get sheets obtained in Examples 1 to 3 and Comparative Example 1, and the results are shown in the table.
応力緩和性:
JIS R3453−1985の試験方法に従って試験
温度150℃で試験を行い、初期応力に対する残留応力
の割合を求めた。Stress Relaxation: A test was conducted at a test temperature of 150° C. according to the test method of JIS R3453-1985, and the ratio of residual stress to initial stress was determined.
水シール性:
ASTM F37 (シール性試験方法)に準じた試験
装置に打抜き試験片90−74φを治具間にセットし、
締めつけ面圧50 kg / cJを与え、内部水圧を
0.5kg/adから0.5kir/−のステップで上
昇させ、各上昇水圧毎に15分間維持し水漏れが発生す
る内部水圧を調べる。水漏れ発生の有無は目視により行
う。Water sealability: A punched test piece 90-74φ was set between jigs in a test device according to ASTM F37 (Sealability test method).
Apply a tightening surface pressure of 50 kg/cJ, increase the internal water pressure in steps from 0.5 kg/ad to 0.5 kir/-, maintain it for 15 minutes for each increase in water pressure, and check the internal water pressure at which water leakage occurs. Visually check for water leakage.
耐熱性:
20 m* X 50 mvsの試験片を200℃X1
6hr加熱処理し、取出後常温まで放置した後、圧縮率
、復元率、重量減少率、厚さ減少率を測定した。Heat resistance: 20 m* x 50 mvs test piece at 200℃ x 1
After being heat-treated for 6 hours and left to stand at room temperature after being taken out, the compression rate, recovery rate, weight reduction rate, and thickness reduction rate were measured.
特許出願人 日本ラインツ株式会社 阿波製紙株式会社 Patent applicant: Nihon Reinz Co., Ltd. Awa Paper Co., Ltd.
Claims (1)
系耐熱性繊維10〜50重量部、有機高分子結合剤2〜
15重量部、および無機充填剤30〜90重量部からな
る成分比組成物の水分散液を抄造することを特徴とする
非アスベスト系ビーターシートの製造方法。 2、非アスベスト系耐熱性繊維が無機繊維である特許請
求の範囲第1項に記載の製造方法。[Claims] 1. 0.5 to 10 parts by weight of cellulose fiber, 10 to 50 parts by weight of non-asbestos heat-resistant fiber, 2 to 5 parts by weight of organic polymer binder.
1. A method for producing a non-asbestos beater sheet, which comprises producing an aqueous dispersion of a component ratio composition comprising 15 parts by weight of an inorganic filler and 30 to 90 parts by weight of an inorganic filler. 2. The manufacturing method according to claim 1, wherein the non-asbestos heat-resistant fiber is an inorganic fiber.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1156487A JPS63182499A (en) | 1987-01-20 | 1987-01-20 | Production of non-asbestos type beater sheet |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1156487A JPS63182499A (en) | 1987-01-20 | 1987-01-20 | Production of non-asbestos type beater sheet |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS63182499A true JPS63182499A (en) | 1988-07-27 |
Family
ID=11781432
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1156487A Pending JPS63182499A (en) | 1987-01-20 | 1987-01-20 | Production of non-asbestos type beater sheet |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63182499A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1065253A1 (en) * | 1999-06-30 | 2001-01-03 | Omniafiltra Cartiera del Torano S.p.a. | Sealing gasket material in roll produced with the beater addition technique |
JP2006242044A (en) * | 2005-03-01 | 2006-09-14 | Mazda Motor Corp | Oil pump device for engine |
JP2007512473A (en) * | 2003-11-20 | 2007-05-17 | ドレッサ、インク | Gasket with push rod retainer |
-
1987
- 1987-01-20 JP JP1156487A patent/JPS63182499A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1065253A1 (en) * | 1999-06-30 | 2001-01-03 | Omniafiltra Cartiera del Torano S.p.a. | Sealing gasket material in roll produced with the beater addition technique |
JP2007512473A (en) * | 2003-11-20 | 2007-05-17 | ドレッサ、インク | Gasket with push rod retainer |
JP2006242044A (en) * | 2005-03-01 | 2006-09-14 | Mazda Motor Corp | Oil pump device for engine |
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