JPH0125708B2 - - Google Patents
Info
- Publication number
- JPH0125708B2 JPH0125708B2 JP57232353A JP23235382A JPH0125708B2 JP H0125708 B2 JPH0125708 B2 JP H0125708B2 JP 57232353 A JP57232353 A JP 57232353A JP 23235382 A JP23235382 A JP 23235382A JP H0125708 B2 JPH0125708 B2 JP H0125708B2
- Authority
- JP
- Japan
- Prior art keywords
- fire
- flame
- polyethylene
- retardant
- plastic
- 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
- 229920003023 plastic Polymers 0.000 claims description 16
- 239000004033 plastic Substances 0.000 claims description 16
- 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 claims description 10
- 239000003063 flame retardant Substances 0.000 claims description 10
- 239000000839 emulsion Substances 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 9
- 230000009970 fire resistant effect Effects 0.000 claims description 8
- 239000011247 coating layer Substances 0.000 claims description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 5
- 229910052760 oxygen Inorganic materials 0.000 claims description 5
- 239000001301 oxygen Substances 0.000 claims description 5
- 239000000835 fiber Substances 0.000 claims description 4
- 150000002366 halogen compounds Chemical class 0.000 claims description 4
- 239000011256 inorganic filler Substances 0.000 claims description 3
- 229910003475 inorganic filler Inorganic materials 0.000 claims description 3
- -1 polyethylene Polymers 0.000 description 20
- 239000004698 Polyethylene Substances 0.000 description 11
- 229920000573 polyethylene Polymers 0.000 description 11
- 239000004743 Polypropylene Substances 0.000 description 8
- 229920001155 polypropylene Polymers 0.000 description 8
- 239000011248 coating agent Substances 0.000 description 7
- 238000000576 coating method Methods 0.000 description 7
- 239000003973 paint Substances 0.000 description 7
- 229920000114 Corrugated plastic Polymers 0.000 description 4
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 4
- 239000000155 melt Substances 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 102000004190 Enzymes Human genes 0.000 description 2
- 108090000790 Enzymes Proteins 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- WRDNCFQZLUCIRH-UHFFFAOYSA-N 4-(7-azabicyclo[2.2.1]hepta-1,3,5-triene-7-carbonyl)benzamide Chemical compound C1=CC(C(=O)N)=CC=C1C(=O)N1C2=CC=C1C=C2 WRDNCFQZLUCIRH-UHFFFAOYSA-N 0.000 description 1
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 229920006222 acrylic ester polymer Polymers 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 150000001463 antimony compounds Chemical class 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical class OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000000875 corresponding effect Effects 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 239000004703 cross-linked polyethylene Substances 0.000 description 1
- WHHGLZMJPXIBIX-UHFFFAOYSA-N decabromodiphenyl ether Chemical compound BrC1=C(Br)C(Br)=C(Br)C(Br)=C1OC1=C(Br)C(Br)=C(Br)C(Br)=C1Br WHHGLZMJPXIBIX-UHFFFAOYSA-N 0.000 description 1
- HDERJYVLTPVNRI-UHFFFAOYSA-N ethene;ethenyl acetate Chemical group C=C.CC(=O)OC=C HDERJYVLTPVNRI-UHFFFAOYSA-N 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 238000004079 fireproofing Methods 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000012796 inorganic flame retardant Substances 0.000 description 1
- 239000010410 layer Substances 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
- ZADYMNAVLSWLEQ-UHFFFAOYSA-N magnesium;oxygen(2-);silicon(4+) Chemical compound [O-2].[O-2].[O-2].[Mg+2].[Si+4] ZADYMNAVLSWLEQ-UHFFFAOYSA-N 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A30/00—Adapting or protecting infrastructure or their operation
- Y02A30/14—Extreme weather resilient electric power supply systems, e.g. strengthening power lines or underground power cables
Landscapes
- Insulated Conductors (AREA)
- Laminated Bodies (AREA)
Description
本発明は難燃性プラスチツク管に係り、特に、
電線・ケーブルを挿入して保護する電線管に用い
て好適な難燃性プラスチツク管に関するものであ
る。
従来、電線・プラスチツクを布設する場合、そ
の機械的保護のために、電線・ケーブルを電線管
の中に挿入して布設することがある。特に、プラ
ント建設現場で仮配線するような場所では、電
線・ケーブルの保護が必要である。
このような電線管としては、従来、金属製パイ
プあるいはセラミツク製パイプが用いられてき
た。しかし、近年、可撓性や経済性に富み、かつ
軽量である等の特徴をもつ波付きプラスチツク製
パイプが用いられるようになつた。その代表的な
ものはポリエチレン管、ポリプロピレン管等であ
る。
しかし、これらのプラスチツク管は、耐火性に
乏しく、溶接花火やその他の火により容易に燃焼
し、ケーブルを損傷し易いという欠点を有してい
る。そのため、ポリエチレンあるいはポリプロピ
レンの難燃化が検討されているが、このようなプ
ラスチツク自体を難燃化すると機械的強度や耐摩
耗性が低下し、ポリエチレンあるいはポリプロピ
レン本来の特徴が失われてしまうという難点があ
つた。
本発明の目的は、上記難点を解消し、耐火性に
すぐれた難燃性プラスチツク管を提供することに
ある。
本発明は、プラスチツク管の外側に水性エマル
ジヨン、ハロゲン化合物、無機充填剤および防炎
性繊維を主体とし、酵素指数が30以上の耐火性組
成物による被覆層を設けてなることを特徴とする
ものである。
上記耐火性組成物の構成成分である水性エマル
ジヨン樹脂は、ポリ酢酸ビニルエマルジヨン、酢
酸ビニル−エチレンコポリマーエマルジヨン、酢
酸ビニル−プロピオン酸ビニルコポリマーエマル
ジヨン−酢酸ビニル−塩化ビニルコポリマーエマ
ルジヨン−酢酸ビニル−アクリレートコポリマー
エマルジヨン、アクリル酸エステルポリマーエマ
ルジヨン(自己架橋タイプを含む)等が望まし
い。この水性エマルジヨン樹脂は被覆層を形成さ
せる塗膜の結合剤であるが、一般に可燃物である
ため最少限の使用が好ましく、エマルジヨン樹脂
分として乾燥塗膜総重量の15〜35重量%の範囲が
適している。
ハロゲン化合物としては、たとえば、塩化パラ
フイン、塩素化ナフタリン、デカブロモジフエニ
ルオキサイド、ポリブロモビスフエニル、ビスグ
ワニジンテトラブロモフタレート、1,2,5,
6,9,10−ヘキサブロモシクロドデカン、トリ
ス−β−クロロエチルホスフエート等があり、こ
れらを組合わせて使用してもよく、その量は乾燥
塗膜総重量の1.5〜15重量%が適している。ハロ
ゲン化合物とアンチモン化合物、たとえば、三酸
化アンチモンを組合わせると耐火効果が増大する
ので三酸化アンチモンを併用するのが望ましい。
無機充填剤には、たとえば、炭酸カルシウム、
酸化アルミニウム、水酸化アルミニウム、珪酸マ
グネシウム、珪酸アルミニウム、シリカ、硼酸亜
沿、りん酸塩フリツト等がある。これらの不燃物
は耐火性組成物の骨格をなすもので、乾燥塗膜総
重量の40〜70重量%含むことが望ましい。
防炎性繊維としては、カイノール(日本カイノ
ール(株)製品)、ポリ−P−フエニレンテレフタル
アミド繊維、ガラス繊維、アスベスト等があり、
その添加量は乾燥塗膜総重量の0.2〜5重量%が
適している。さらに必要であれば各種の顔料、可
塑剤、増粘剤、界面活性剤、殺菌剤等を含有させ
てもよい。
上記の成分を配合して耐火性組成物による防火
塗料を調整するが、乾燥塗膜の酸素指数は30以上
に調整すべきであり、酵素指数が30以下では十分
な耐火効果が得られない。
この発明に使用するプラスチツク管の材質は、
高分子量のものが好ましく、分子量が高い程耐熱
性が良く、加熱されたときの溶融変形が少く、ま
た機械的強度もすぐれている。たとえばポリエチ
レンの場合はメルトインデツクスが0.3以下、ポ
リプロピレンの場合にはメルトフローレツトが5
以下のものが望ましい。プラスチツク管を波付き
にする目的は可撓性を改善するためである。
以下、本発明の実施例を図に基づいて説明す
る。図において、1は耐火性組成物による被覆
層、2は波付きプラスチツク管、3はケーブル、
4はリボンタイプガスバーナである。
実施例 1
密度0.95、メルトインデツクス0.04の高密度ポ
リエチレンを用いて外径127mm、厚さ2.5mm、波の
高さ13mmの波付きポリエチレン管2を作成する。
次に第1表(1)の組成の防火塗料(塗膜の酸素指
数42)を管2の表面に塗布して、乾燥後の厚さ1
mmの被覆層1を形成させる。この管2の中心に3
心×150mm2架橋ポリエチレン絶縁ビニルシースケ
ーブル3を挿入し、その上端を封止する。この試
験体(長さ2400mm)を図に示すように垂直に設置
し、リボンタイプガスバーナー4の炎により20分
間加熱した。その結果炎の当つた部分のポリエチ
レンが溶融変形しただけで、内部のケーブル3は
殆んど損傷を受けなかつた。
実施例 2
密度0.89、メルトフローレート1.0のポリプロ
ピレンを用い上記と同じ形状の波付きポリプロピ
レン管を作成する。
次に第1表(2)の組成の防火塗料(塗膜の酸素数
40)を管の表面に塗布して、乾燥後の厚さ1mmの
被覆層を形成させる。この試験体を用いて実施例
1と同様の加熱試験を行つた結果、炎の当つた部
分のポリプロピレン管が溶融変形しただけで内部
のケーブルは殆んど損傷を受けなかつた。
比較例
実施例1の波付きポリエチレン管の表面に、第
1表(3)の組成の塗料(塗膜の酸素指数25)を乾燥
後の厚さが1.0mmになるように塗布し、この試験
体を用いて実施例1と同様の加熱試験を行つた結
果、ポリエチレン管およびケーブルの延焼を防止
することができなかつた。
FIELD OF THE INVENTION The present invention relates to flame retardant plastic pipes, and more particularly to:
This invention relates to a flame-retardant plastic tube suitable for use as a conduit for inserting and protecting electric wires and cables. Conventionally, when laying electric wires or plastic, the electric wires or cables are sometimes inserted into conduits for mechanical protection. In particular, it is necessary to protect electric wires and cables at locations where temporary wiring is performed at plant construction sites. Conventionally, metal pipes or ceramic pipes have been used as such electric conduits. However, in recent years, corrugated plastic pipes have come into use because they are flexible, economical, and lightweight. Typical examples include polyethylene pipes and polypropylene pipes. However, these plastic tubes have the disadvantage that they have poor fire resistance and are easily combusted by welding fireworks or other fires, which can easily damage the cable. For this reason, making polyethylene or polypropylene flame-retardant is being considered, but the drawback is that making such plastics themselves flame-retardant reduces mechanical strength and abrasion resistance, and the original characteristics of polyethylene or polypropylene are lost. It was hot. SUMMARY OF THE INVENTION An object of the present invention is to solve the above-mentioned problems and provide a flame-retardant plastic pipe with excellent fire resistance. The present invention is characterized in that a coating layer is provided on the outside of the plastic tube with a fire-resistant composition mainly consisting of an aqueous emulsion, a halogen compound, an inorganic filler, and flame-retardant fibers, and having an enzyme index of 30 or more. It is. The aqueous emulsion resin that is a component of the fire-resistant composition is polyvinyl acetate emulsion, vinyl acetate-ethylene copolymer emulsion, vinyl acetate-vinyl propionate copolymer emulsion-vinyl acetate-vinyl chloride copolymer emulsion-vinyl acetate - Acrylate copolymer emulsions, acrylic ester polymer emulsions (including self-crosslinking types), etc. are desirable. This water-based emulsion resin is a binder for the coating film that forms the coating layer, but since it is generally flammable, it is preferable to use it at a minimum, and the emulsion resin content should be in the range of 15 to 35% by weight of the total weight of the dry coating film. Are suitable. Examples of halogen compounds include chlorinated paraffin, chlorinated naphthalene, decabromodiphenyl oxide, polybromobisphenyl, bisguwanidine tetrabromophthalate, 1,2,5,
There are 6,9,10-hexabromocyclododecane, tris-β-chloroethyl phosphate, etc., and these may be used in combination, and the appropriate amount is 1.5 to 15% by weight of the total weight of the dry coating film. ing. Combining a halogen compound and an antimony compound, such as antimony trioxide, increases the fireproofing effect, so it is desirable to use antimony trioxide in combination. Inorganic fillers include, for example, calcium carbonate,
Examples include aluminum oxide, aluminum hydroxide, magnesium silicate, aluminum silicate, silica, boric acid salt, phosphate frit, etc. These noncombustible substances form the framework of the fire-resistant composition, and preferably contain 40 to 70% by weight of the total weight of the dry coating film. Examples of flame-retardant fibers include Kynor (product of Nippon Kynor Co., Ltd.), poly-P-phenylene terephthalamide fiber, glass fiber, and asbestos.
The amount added is suitably 0.2 to 5% by weight based on the total weight of the dry coating film. Furthermore, if necessary, various pigments, plasticizers, thickeners, surfactants, bactericides, etc. may be included. The above ingredients are blended to prepare a fire-resistant paint made of a fire-resistant composition, but the oxygen index of the dry paint film should be adjusted to 30 or more, and if the enzyme index is less than 30, a sufficient fire-resistant effect will not be obtained. The material of the plastic tube used in this invention is
High molecular weight is preferred; the higher the molecular weight, the better the heat resistance, the less melting deformation when heated, and the better the mechanical strength. For example, polyethylene has a melt index of 0.3 or less, and polypropylene has a melt flow rate of 5.
The following are desirable. The purpose of corrugating plastic tubing is to improve its flexibility. Embodiments of the present invention will be described below based on the drawings. In the figure, 1 is a coating layer made of a fire-resistant composition, 2 is a corrugated plastic pipe, 3 is a cable,
4 is a ribbon type gas burner. Example 1 A corrugated polyethylene pipe 2 having an outer diameter of 127 mm, a thickness of 2.5 mm, and a corrugation height of 13 mm is prepared using high-density polyethylene having a density of 0.95 and a melt index of 0.04. Next, a fire protection paint with the composition shown in Table 1 (1) (oxygen index of the coating film: 42) is applied to the surface of the pipe 2, and after drying, the thickness is 1
A coating layer 1 of mm is formed. 3 in the center of this tube 2
Insert the cross - linked polyethylene insulated vinyl sheath cable 3 with 150 mm core and seal its upper end. This test specimen (length 2400 mm) was placed vertically as shown in the figure and heated with the flame of a ribbon type gas burner 4 for 20 minutes. As a result, the polyethylene in the portion hit by the flame was only melted and deformed, and the internal cable 3 suffered almost no damage. Example 2 A corrugated polypropylene tube having the same shape as above was created using polypropylene with a density of 0.89 and a melt flow rate of 1.0. Next, fire prevention paint with the composition shown in Table 1 (2) (oxygen number in the coating film)
40) is applied to the surface of the tube to form a coating layer with a thickness of 1 mm after drying. A heating test similar to that in Example 1 was conducted using this specimen, and as a result, only the polypropylene tube in the portion hit by the flame was melted and deformed, and the internal cable was hardly damaged. Comparative Example A paint having the composition shown in Table 1 (3) (oxygen index of the paint film: 25) was applied to the surface of the corrugated polyethylene pipe of Example 1 so that the thickness after drying was 1.0 mm, and this test was conducted. As a result of conducting a heating test similar to that in Example 1 using a polyethylene pipe, it was not possible to prevent the spread of fire to the polyethylene pipe and cable.
【表】【table】
【表】
参考例
防火塗料を塗布しない波付きポリエチレン管を
用いて実施例1と同様の加熱試験を行つた結果、
5分間で上部まで延焼、10分間で内部のケーブル
も全焼した。
上記の実施例は波付きプラスチツキ管の耐火処
理について述べたものであるが、平滑なプラスチ
ツク管に適用しても同様の効果を奏することがで
きる。
また、プラスチツク管の材質はポリエチレン、
ポリプロピレンに限定されるものではなく、ビル
ル、ゴム等の管についてもそれ相応の効果を得る
ことができる。
以上説明したように、本発明によれば、プラス
チツク管の機械的強度や耐摩耗性を低下させるこ
となく耐火性にすぐれた難粘性プラスチツク管と
して、実用的効果を発揮することができる。[Table] Reference example The results of a heating test similar to Example 1 using a corrugated polyethylene pipe without fire-retardant paint applied were as follows.
The fire spread to the top within 5 minutes, and the internal cables were completely destroyed within 10 minutes. Although the above-mentioned embodiment describes the fireproof treatment of a corrugated plastic pipe, the same effect can be achieved even when applied to a smooth plastic pipe. In addition, the material of the plastic pipe is polyethylene,
The present invention is not limited to polypropylene, and corresponding effects can also be obtained with tubes made of virure, rubber, etc. As explained above, according to the present invention, a practical effect can be exhibited as a low-viscosity plastic pipe with excellent fire resistance without reducing the mechanical strength or wear resistance of the plastic pipe.
図は本発明の実施例を説明するための難燃性プ
ラスチツク管の縦断面図である。
1:被覆層、2:波付きプラスチツク管、3:
ケーブル、4:リボンタイプガスバーナー。
The figure is a longitudinal cross-sectional view of a flame-retardant plastic tube for explaining an embodiment of the present invention. 1: Covering layer, 2: Corrugated plastic tube, 3:
Cable, 4: Ribbon type gas burner.
Claims (1)
ハロゲン化合物、無機充填剤および防炎性繊維を
主体とし、酸素指数が30以上の耐火性組成物によ
る被覆層を設けてなることを特徴とする難燃性プ
ラスチツク管。1 Aqueous emulsion on the outside of the plastic tube,
1. A flame-retardant plastic pipe comprising a halogen compound, an inorganic filler, and a flame-retardant fiber as main components, and a coating layer made of a fire-resistant composition having an oxygen index of 30 or more.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57232353A JPS59123652A (en) | 1982-12-28 | 1982-12-28 | Flame-retarded plastic pipe |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57232353A JPS59123652A (en) | 1982-12-28 | 1982-12-28 | Flame-retarded plastic pipe |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59123652A JPS59123652A (en) | 1984-07-17 |
JPH0125708B2 true JPH0125708B2 (en) | 1989-05-18 |
Family
ID=16937875
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP57232353A Granted JPS59123652A (en) | 1982-12-28 | 1982-12-28 | Flame-retarded plastic pipe |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59123652A (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ATE68254T1 (en) * | 1988-08-29 | 1991-10-15 | Geberit Ag | PLASTIC FITTING FOR PIPE SYSTEMS. |
-
1982
- 1982-12-28 JP JP57232353A patent/JPS59123652A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS59123652A (en) | 1984-07-17 |
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