JPS62220555A - Sheet for molding mechanical closure case of cable - Google Patents
Sheet for molding mechanical closure case of cableInfo
- Publication number
- JPS62220555A JPS62220555A JP6458186A JP6458186A JPS62220555A JP S62220555 A JPS62220555 A JP S62220555A JP 6458186 A JP6458186 A JP 6458186A JP 6458186 A JP6458186 A JP 6458186A JP S62220555 A JPS62220555 A JP S62220555A
- Authority
- JP
- Japan
- Prior art keywords
- sheet
- resin
- glass fibers
- weight
- case
- 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
- 238000000465 moulding Methods 0.000 title claims 2
- 239000003365 glass fiber Substances 0.000 claims abstract description 22
- -1 polyethylene Polymers 0.000 claims abstract description 11
- 239000004114 Ammonium polyphosphate Substances 0.000 claims abstract description 6
- 239000004640 Melamine resin Substances 0.000 claims abstract description 6
- 229920000877 Melamine resin Polymers 0.000 claims abstract description 6
- 235000019826 ammonium polyphosphate Nutrition 0.000 claims abstract description 6
- 229920001276 ammonium polyphosphate Polymers 0.000 claims abstract description 6
- 229920005992 thermoplastic resin Polymers 0.000 claims abstract description 6
- 239000000454 talc Substances 0.000 claims abstract description 3
- 229910052623 talc Inorganic materials 0.000 claims abstract description 3
- 239000000203 mixture Substances 0.000 claims description 5
- 239000004254 Ammonium phosphate Substances 0.000 claims description 3
- 229910019142 PO4 Inorganic materials 0.000 claims description 3
- 235000019289 ammonium phosphates Nutrition 0.000 claims description 3
- 239000000843 powder Substances 0.000 claims description 2
- 229920005989 resin Polymers 0.000 abstract description 11
- 239000011347 resin Substances 0.000 abstract description 11
- 229910052736 halogen Inorganic materials 0.000 abstract description 4
- 150000002367 halogens Chemical class 0.000 abstract description 4
- 239000004698 Polyethylene Substances 0.000 abstract description 2
- 239000007789 gas Substances 0.000 abstract description 2
- 229920000573 polyethylene Polymers 0.000 abstract description 2
- 230000001473 noxious effect Effects 0.000 abstract 1
- 239000002245 particle Substances 0.000 abstract 1
- 230000000694 effects Effects 0.000 description 8
- 239000003063 flame retardant Substances 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 6
- 238000000034 method Methods 0.000 description 5
- 239000004033 plastic Substances 0.000 description 5
- 229920003023 plastic Polymers 0.000 description 5
- 239000004743 Polypropylene Substances 0.000 description 4
- 229920001155 polypropylene Polymers 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 229910000831 Steel Inorganic materials 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910000077 silane Inorganic materials 0.000 description 2
- 239000002341 toxic gas Substances 0.000 description 2
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 208000037062 Polyps Diseases 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- RJZNFXWQRHAVBP-UHFFFAOYSA-I aluminum;magnesium;pentahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Al+3] RJZNFXWQRHAVBP-UHFFFAOYSA-I 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 210000003127 knee Anatomy 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Substances OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000012756 surface treatment agent Substances 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明はケーブルのメカニカルジヨイントのケ特に有害
なハロゲンガスf:R生じないメカニカルジヨイントに
用いられるケースに関するものである。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a case for use in mechanical joints of cables, in particular mechanical joints which do not generate harmful halogen gas f:R.
従来の技術
通信ケーブル等ケーブルの接続工法には種々の方法があ
るが、メカニカルクロージヤーを使用して機械的に組立
てる方法り火を使用することなくゼルト、ナツトによっ
て組立てる構改であるところから注目され始めている。Conventional technology There are various methods for connecting cables such as communication cables, but this method is attracting attention because it is assembled mechanically using a mechanical closure and is assembled using bolts and nuts without using a torch. It's starting to happen.
このような目的でケーブルのメカ二カルジョイント工法
が注目され、これに用いられるクロージヤー用ケースと
して不燃性でしかも丈夫なプラスチックケースが要求さ
れている。For this purpose, the cable mechanical joint construction method has attracted attention, and a nonflammable and durable plastic case is required as the closure case used for this method.
ところが、ここに用いられるケース材料を不燃化するに
は通常はプラスチック中にハロゲン系難燃剤を配合する
か、水酸化アルミニウム又は水酸化マグネシウムを配合
し、更に機械的強度を増すためにはガラス繊維等を混入
することが考えられている。However, to make the case material used here nonflammable, halogen-based flame retardants are usually added to the plastic, or aluminum hydroxide or magnesium hydroxide is added to the plastic, and to further increase mechanical strength, glass fiber is added. It is considered that the mixture of
しかしながらプラスチック中にノ・ロゲン系難燃剤を配
合すると、燃焼時に有毒ガスを発生する欠点があυ、又
氷水酸化アルミニウム水酸化マグネシウム等全配合する
と、プラスチック組底物とガラス繊維の濡れ性を阻害し
、空気の流通路を作るために本来気密であるべきクロー
ジヤー用ケースとしては重大な欠点を有するものと言わ
ざるを得ない。However, when a chlorine-based flame retardant is blended into plastic, it has the disadvantage of generating toxic gas when burned, and when it is blended with ice hydroxide, aluminum magnesium hydroxide, etc., it inhibits the wettability of plastic bottoms and glass fibers. However, it must be said that this case has a serious drawback as a case for a closure, which should be airtight in order to create an air flow path.
問題点を解決するための手段
本発明は上記問題点を解決するために鋭意研究の結果な
されたもので、その概要は下記のとおりである。Means for Solving the Problems The present invention has been made as a result of intensive research to solve the above problems, and the outline thereof is as follows.
熱可塑性樹脂にポリリン酸アンモニウム又はリン酸エス
テルと、微粉末メラミン樹脂とを添加した組成を主とし
、これにだラス繊#全分散せしめてなるメカニカルクロ
ージヤーケース底形用シートである。そしてその好まし
い配合について更に詳述すれば以下のとおシである。This is a sheet for the bottom shape of a mechanical closure case, which is mainly composed of a thermoplastic resin, ammonium polyphosphate or phosphoric acid ester, and finely powdered melamine resin, and is made by completely dispersing lass fibers therein. Further details of the preferred formulation are as follows.
熱可塑性樹脂はケース底形用シートの基本材料であるが
一般には低コストで加工し易いものが還択される。従っ
てこれにはポリエチレン、ポリプロピレン、エチレンプ
ロピレン共重合体等が好ましく、塩ビ系の樹脂は火災時
に塩素を発生する点から余シ好ましいものとは言えない
。Thermoplastic resin is the basic material for the sheet for the case bottom shape, and in general, those that are low cost and easy to process are selected. Therefore, polyethylene, polypropylene, ethylene propylene copolymer, etc. are preferable for this purpose, and vinyl chloride resins are not particularly preferable because they generate chlorine in the event of a fire.
そしてこの熱可塑性樹脂は70重景%を越えると、他の
配合剤が少なくなり過ぎて難燃効果を低下し機械的強度
も低下する。又、35重fgq6より少ない場合は加工
性が悪くなりシート形成には不適当となる。If the thermoplastic resin exceeds 70% by weight, the amount of other compounding ingredients becomes too small, resulting in a decrease in flame retardant effect and a decrease in mechanical strength. If the weight is less than 35 fgq6, the processability will be poor and it will be unsuitable for sheet formation.
ポリリン酸アンモニウム又はリン酸エステルは非ハロゲ
ン系の難燃剤で、しかもガラス繊維との濡れ性もよく、
このためシートに充分な難燃効果を与えることができる
。Ammonium polyphosphate or phosphate ester is a non-halogen flame retardant and has good wettability with glass fibers.
Therefore, a sufficient flame retardant effect can be imparted to the sheet.
5重′Mkcs未満ではその効果が不充分であシ、25
重量%を越えると過剰にして離燃性の向上に関係のない
配合tを含むこととなシコストアップとともにケースの
可撓性を損な゛うことになる。If it is less than 5'Mkcs, the effect is insufficient, and 25
If it exceeds the weight percentage, it will contain an excessive amount of the compound t which has nothing to do with improving the flammability, increasing the cost and impairing the flexibility of the case.
微粉末メラミン樹脂は例えば10μ以下のものが充分分
散され易く好ましく、又、分子中のN成分が火焔にあっ
ても難燃作用を発揮し、かつ前記リン酸系の化合物とメ
ラミン樹脂とは相剰効果によシ動燃作用を高めることが
認められる。For example, fine powder melamine resin of 10μ or less is preferable because it is easily dispersed, and the N component in the molecule exhibits a flame retardant effect even when exposed to flame, and the phosphoric acid compound and melamine resin are compatible. It is recognized that the residual effect increases the dynamic and combustion effect.
次にタルクはケースの製造に際し、増量と加工とに寄与
するものである。Next, talc contributes to weight increase and processing during case manufacturing.
ガラス繊維は通常プラスチックの強化に用いられる25
μφ程度のものを17〜25重fal配合することがシ
・−トの可撓性を保持しながら機械的強度も高めるので
好ましい。17重重量未満ではその作用が不充分であり
、25重g’sを越えると徒らにガラス繊維の址が多く
なるだけである。Glass fiber is commonly used to strengthen plastics25
It is preferable to mix 17 to 25 folds of about .mu.φ because this increases the mechanical strength while maintaining the flexibility of the sheet. If the weight is less than 17 g's, the effect will be insufficient, and if it exceeds 25 g's, the amount of glass fiber will increase unnecessarily.
次にシートの製造手段の代表例について述べる。Next, typical examples of sheet manufacturing means will be described.
1)ガラスファイ/々−の製造
ガラスファイ/々−’e23μφに紡糸して製造し、次
にシラン系表面処理剤で表面処理し表面を活性化する。1) Manufacture of glass fiber//- A glass fiber//'e23μΦ is produced by spinning, and then surface treated with a silane surface treatment agent to activate the surface.
シラン系表面処理は通常のガラスファイバーの場合よシ
もノぞ−オキサイドリッチで行なう方がよい。It is better to carry out silane-based surface treatment in an oxide-rich manner than in the case of ordinary glass fibers.
このようにした表面処理ガラスファイ/々−70本を撚
合せ又は収束してリールに巻取る。Seventy of the surface-treated glass fibers are twisted or converged and wound onto a reel.
11)ガラスファイノ々−マットの製造第1図に示すよ
うにガラスファイ/クー23μφXフ0本elリールと
したもの一30リールを1台に収め、かくしたもの4台
からなるガラスファイ/々−繰出機lOを用意する。一
方コンベア−11を回転させながら、その上に前記ガラ
スファイ/々−Xiコイル状にしながらコンベアーif
上に一様に落して行き、マット化し、ニーPラー12で
針打ち、切断を行ない巻取りリール13でマット14を
巻取る。11) Manufacture of glass fiber mats As shown in Fig. 1, one glass fiber/coo 23 μφ x 0 reel is housed in one 30 reels, and the glass fiber/mat is made up of 4 units. - Prepare a feeding machine IO. On the other hand, while rotating the conveyor 11, the glass fiber/Xi coil is placed on top of the conveyor if
The material is uniformly dropped onto the top, made into a mat, punched and cut with a kneeler 12, and the mat 14 is wound up with a take-up reel 13.
このようにしてできたマット14の状態は第2図の上面
図に示すとおりである。The state of the mat 14 thus produced is as shown in the top view of FIG.
li+ ) シートの製造
第3図に示すように例えばポリプロピレン16を押出機
15よシシート状に押出し、同時に前記11)で製造さ
れたガラスファイ/:!−マツ)14をその上下両面か
ら供給し、更に、その外方から厚さ0.5+u+a度の
ポリプロビレ/フィルム17’)供給し、ラミネーター
に入る。ラミネーターは1対の厚さ2〜3uのスチール
ペル)18からなり、上下より挾んで加工し接着させる
。加圧は約5 Ky/crn2で行なわれ上部のスチー
ルベルトには最初の部分は加熱部19、後の部分は冷却
部20とし。li+) Production of Sheet As shown in FIG. 3, for example, polypropylene 16 is extruded into a sheet by an extruder 15, and at the same time, the glass fiber produced in 11) is produced. - Pine) 14 is supplied from both the upper and lower surfaces, and a polypropylene/film 17') having a thickness of 0.5+U+A degrees is supplied from the outside, and then enters the laminator. The laminator consists of a pair of steel pels 18 with a thickness of 2 to 3 μm, which are sandwiched from above and below to process and adhere. Pressure was applied at approximately 5 Ky/crn2, and the upper steel belt was heated at the heating section 19 at the beginning and at the cooling section 20 at the rear.
加熱部では約350℃で加熱され、サンドインチ状のも
のが樹脂の溶融で一体化され、冷却により°固化する。In the heating section, the resin is heated to about 350°C, and the sandwich-shaped pieces are melted and integrated with the resin, and then solidified by cooling.
しかる後ラミネーターから進行方向に出たところでカッ
ター21によシ所定の長さに切断されてシートを得る。Thereafter, the sheet is cut into a predetermined length by a cutter 21 when it comes out of the laminator in the direction of travel to obtain a sheet.
ここに用いられる樹脂は勿論ポリプロピレンに限定され
ないが、押出機に供給するものH,MIが2〜3の小さ
いものがよい。 もしもJが余り大きいとガラスマット
のストランドの7アイ/々−1本1本に樹脂が入シにぐ
くストランド表面のみに樹脂が入るからである。The resin used here is of course not limited to polypropylene, but it is preferable to use a resin with a small H and MI of 2 to 3 to be fed to the extruder. This is because if J is too large, the resin will enter only the surface of each strand of the glass mat.
又、上記本発明に係るシートは加熱変形加工されて、中
空の管状体(ケーブルのメカニカルクロージヤー用ケー
スンが容易に形成される。Further, the sheet according to the present invention is heated and deformed to easily form a hollow tubular body (a casen for a mechanical closure of a cable).
次に本発明によるシートの性能を確認するための試作試
験例について述べる。Next, a prototype test example for confirming the performance of the sheet according to the present invention will be described.
試験1、実施例■に示した組成の配合で製造した防火性
シート(厚さ5〜6 U)からなる密閉型ケースを作成
し、このケース内にエア(1,5Kq/crn2)を入
れて水中で漏れを観察した結果洩れはなかった。A sealed case made of a fireproof sheet (thickness 5 to 6 U) manufactured with the composition shown in Test 1, Example As a result of observing the leakage underwater, there was no leakage.
試験2.実施例りに示した組成の配合で製造し次防火性
シート(厚さ5〜6 m )からなる密閉型ケースを作
成し、この中にエア(t、o h/cm2)を入れて、
内圧を連続モニターしながら、ヒートサイクル(−20
〜+60℃、2サイクル/日)50サイクルを印加した
結果洩れは殆んど観察されず、水中での漏れも観察され
なかった。Test 2. A sealed case made of a fireproof sheet (thickness 5 to 6 m) was prepared using the composition shown in the example, and air (t, oh/cm2) was introduced into the case.
While continuously monitoring the internal pressure, heat cycle (-20
As a result of applying 50 cycles (~+60°C, 2 cycles/day), almost no leakage was observed, and no leakage in water was observed.
試験3、実施例1と実施例3の配合により第4図に示す
ように厚さ5朋のシート23を作成して、60 X 6
0 msに切り出し、中央に811jφの穴22aを明
け、第5図に示すようにシートの厚み方向に穴2゛2b
を有する金属パイプ24を前記シート23の穴22aに
嵌合するようにし、その先端をシールするとともにこれ
を水槽25中に入れてエアー(4KII/cm23に矢
印方向に流して水中での漏れを観察し友がシートの表面
・断面からの洩れは観察されなかった。Test 3: A sheet 23 with a thickness of 5 mm was prepared as shown in FIG.
0 ms, a hole 22a of 811jφ in the center, and a hole 2゛2b in the thickness direction of the sheet as shown in Fig. 5.
A metal pipe 24 having a diameter of 4K II was fitted into the hole 22a of the sheet 23, and its tip was sealed, and the pipe was placed in a water tank 25 and air (4KII/cm23) was flowed in the direction of the arrow to observe leakage in the water. No leakage from the surface or cross section of the sheet was observed.
実施例1.2及び3の各試料シートについてトーチラン
プで3分間加熱した後火焔ヲ取り去ったところ5秒以内
に消火した。Each of the sample sheets of Examples 1.2 and 3 was heated with a torch lamp for 3 minutes and then the flame was removed, and the fire extinguished within 5 seconds.
発明の効果
゛本発明によれば以上の試験例から明らかなように、火
災に際して有毒ガスを発生する成分を含有せず、万一の
場合も安全であり、しかも、難燃性で消火能力に優れて
いるばかリアなく、シート中のガラス繊維が配合樹脂と
の濡れ性が良いため、シート中に通気路が生成されず、
この点からも防水性とともに難燃性を補完するものであ
る。Effects of the Invention According to the present invention, as is clear from the above test examples, it does not contain components that generate toxic gas in the event of a fire, is safe even in the event of a fire, and is flame retardant and has excellent fire extinguishing ability. The glass fiber in the sheet has good wettability with the blended resin, so no air passages are created in the sheet.
From this point of view as well, it complements both waterproofness and flame retardancy.
又、このシートは必要な内圧に耐えるケースも容易に底
形加工し得るものであシ、ケーブルのメカニカル・ジヨ
イントのクロージヤー用ケースには非常に有効である。Furthermore, this sheet can be easily shaped into a case that can withstand the necessary internal pressure, and is very effective for cases for closures of mechanical joints of cables.
第1図はガラスマットの製造工程の説明図、第2図はガ
ラスマットの一例を示す上面図、第3図は本発明のシー
トの製造工程例を示す説明図、第4図は試験試料の形状
を示す斜視図、第5図はその試験状態を示す断面図であ
る。
工・・・ガラスファイ/々−,10・・・ガラスファイ
/マー繰出機、11・・・コンベア、12・・・ニー?
ラー1工3・・・巻取りリール、工4・・・マット、1
5・・・押出機、16・・・ポリプロピレン、17・・
・ポリプ四ピレンフィルム、18・・・スチールベルト
、19・・・加熱部、20・・・冷却部、21・・・カ
ッター、22・・・穴、23・・・シート、24・・・
金属パイプ、25・・・水槽。
代理人 弁理士 竹 内 守
第1図Fig. 1 is an explanatory diagram of the manufacturing process of the glass mat, Fig. 2 is a top view showing an example of the glass mat, Fig. 3 is an explanatory diagram showing an example of the manufacturing process of the sheet of the present invention, and Fig. 4 is an illustration of the test sample. A perspective view showing the shape, and FIG. 5 a cross-sectional view showing the test state. Engineering...Glass Fiber/T-, 10...Glass Fiber/Mer feeding machine, 11...Conveyor, 12...Knee?
Ra 1 work 3...take-up reel, work 4...mat, 1
5... Extruder, 16... Polypropylene, 17...
・Polyp tetrapyrene film, 18... Steel belt, 19... Heating section, 20... Cooling section, 21... Cutter, 22... Hole, 23... Sheet, 24...
Metal pipe, 25...Aquarium. Agent Patent Attorney Mamoru Takeuchi Figure 1
Claims (2)
酸エステルと微粉末メラミン樹脂を主とする組成物のシ
ート中にガラス繊維が分散されていることを特徴とする
ケーブルのメカニカルクロージヤーケース成形用シート(1) For molding a mechanical closure case for a cable, characterized in that glass fibers are dispersed in a sheet of a composition mainly consisting of a thermoplastic resin, ammonium polyphosphate or phosphate ester, and finely powdered melamine resin. sheet
モニウム又はリン酸エステル5〜25重量%、微粉末メ
ラミン樹脂5〜35重量%、タルク5〜15重量%、ガ
ラス繊維17〜25重量%とからなる特許請求の範囲第
1項記載のケーブルのメカニカルクロージヤーケース成
形用シート(2) 70-35% by weight of thermoplastic resin, 5-25% by weight of ammonium polyphosphate or phosphate ester, 5-35% by weight of fine powder melamine resin, 5-15% by weight of talc, and 17-25% by weight of glass fiber. A sheet for forming a mechanical closure case for a cable according to claim 1 consisting of
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6458186A JPS62220555A (en) | 1986-03-22 | 1986-03-22 | Sheet for molding mechanical closure case of cable |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6458186A JPS62220555A (en) | 1986-03-22 | 1986-03-22 | Sheet for molding mechanical closure case of cable |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS62220555A true JPS62220555A (en) | 1987-09-28 |
Family
ID=13262351
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6458186A Pending JPS62220555A (en) | 1986-03-22 | 1986-03-22 | Sheet for molding mechanical closure case of cable |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62220555A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01203468A (en) * | 1988-02-10 | 1989-08-16 | Marubishi Yuka Kogyo Kk | Flame-retardant synthetic resin composition |
JPH02128710A (en) * | 1988-11-10 | 1990-05-17 | Daiki:Kk | Bedding |
US5286576A (en) * | 1989-08-21 | 1994-02-15 | The B. F. Goodrich Company | Compression molded flame retardant and high impact strength ultra high molecular weight polyethylene composition |
EP1461383A4 (en) * | 2001-12-05 | 2005-12-28 | Isola Laminate Systems Corp | Thermosetting resin composition for high performance laminates |
-
1986
- 1986-03-22 JP JP6458186A patent/JPS62220555A/en active Pending
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01203468A (en) * | 1988-02-10 | 1989-08-16 | Marubishi Yuka Kogyo Kk | Flame-retardant synthetic resin composition |
JPH02128710A (en) * | 1988-11-10 | 1990-05-17 | Daiki:Kk | Bedding |
US5286576A (en) * | 1989-08-21 | 1994-02-15 | The B. F. Goodrich Company | Compression molded flame retardant and high impact strength ultra high molecular weight polyethylene composition |
EP1461383A4 (en) * | 2001-12-05 | 2005-12-28 | Isola Laminate Systems Corp | Thermosetting resin composition for high performance laminates |
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