JPS6383192A - Fire-proof composition - Google Patents
Fire-proof compositionInfo
- Publication number
- JPS6383192A JPS6383192A JP22786586A JP22786586A JPS6383192A JP S6383192 A JPS6383192 A JP S6383192A JP 22786586 A JP22786586 A JP 22786586A JP 22786586 A JP22786586 A JP 22786586A JP S6383192 A JPS6383192 A JP S6383192A
- Authority
- JP
- Japan
- Prior art keywords
- fire
- proof
- compsn
- flame
- dehydrating agent
- 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
- 239000000203 mixture Substances 0.000 title claims description 12
- 230000009970 fire resistant effect Effects 0.000 claims abstract description 13
- 239000003063 flame retardant Substances 0.000 claims abstract description 11
- 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 abstract description 10
- 239000004215 Carbon black (E152) Substances 0.000 claims abstract description 10
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 10
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 10
- 229920001084 poly(chloroprene) Polymers 0.000 claims abstract description 9
- 239000012024 dehydrating agents Substances 0.000 claims abstract description 8
- 150000005846 sugar alcohols Polymers 0.000 claims description 8
- 239000000463 material Substances 0.000 abstract description 5
- -1 monopentaerythritol) Chemical compound 0.000 abstract description 3
- 239000004254 Ammonium phosphate Substances 0.000 abstract description 2
- 229910000148 ammonium phosphate Inorganic materials 0.000 abstract description 2
- 235000019289 ammonium phosphates Nutrition 0.000 abstract description 2
- 239000003086 colorant Substances 0.000 abstract description 2
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 abstract description 2
- 229920001971 elastomer Polymers 0.000 abstract description 2
- 229940059574 pentaerithrityl Drugs 0.000 abstract description 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 abstract description 2
- 229920003023 plastic Polymers 0.000 abstract description 2
- 239000004033 plastic Substances 0.000 abstract description 2
- 239000004014 plasticizer Substances 0.000 abstract description 2
- 239000005060 rubber Substances 0.000 abstract description 2
- 239000003381 stabilizer Substances 0.000 abstract description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 2
- 239000004902 Softening Agent Substances 0.000 abstract 1
- 239000003963 antioxidant agent Substances 0.000 abstract 1
- 230000003078 antioxidant effect Effects 0.000 abstract 1
- 238000001125 extrusion Methods 0.000 abstract 1
- 238000005187 foaming Methods 0.000 description 7
- 238000003763 carbonization Methods 0.000 description 6
- 238000004898 kneading Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 239000003973 paint Substances 0.000 description 3
- 230000002265 prevention Effects 0.000 description 3
- 229920003020 cross-linked polyethylene Polymers 0.000 description 2
- 239000004703 cross-linked polyethylene Substances 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 239000012212 insulator Substances 0.000 description 2
- 239000013067 intermediate product Substances 0.000 description 2
- 238000004804 winding Methods 0.000 description 2
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 1
- 239000004114 Ammonium polyphosphate Substances 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- 235000019826 ammonium polyphosphate Nutrition 0.000 description 1
- 229920001276 ammonium polyphosphate Polymers 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000007765 extrusion coating Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- XFZRQAZGUOTJCS-UHFFFAOYSA-N phosphoric acid;1,3,5-triazine-2,4,6-triamine Chemical compound OP(O)(O)=O.NC1=NC(N)=NC(N)=N1 XFZRQAZGUOTJCS-UHFFFAOYSA-N 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
Landscapes
- Fireproofing Substances (AREA)
- 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、電線・ケーブル、その他の可燃性物の延焼を
防止するための耐火層を形成する耐火組成物、特に、高
難燃性であることから優れた耐火性能を有する耐火層を
形成できる耐火組成物に関するものである。Detailed Description of the Invention [Field of Industrial Application] The present invention relates to a fire-resistant composition that forms a fire-resistant layer for preventing the spread of fire to electric wires, cables, and other combustible materials, particularly a highly flame-retardant composition. The present invention relates to a fire-resistant composition capable of forming a fire-resistant layer having excellent fire-resistant performance.
[従来の技術]
電線・ケーブル、その他の可燃性物を、火災が発生した
場合に延焼から防止する方法として、防火塗料の塗布や
耐火テープあるいはシートの巻回といった方法が従来か
ら採用されてきている。[Prior Art] As a method of preventing the spread of fire to electric wires, cables, and other combustible materials in the event of a fire, methods such as applying fire-retardant paint and wrapping fire-resistant tape or sheets have traditionally been adopted. There is.
[発明が解決しようとする問題点]
防火塗料による方法では、防火塗料の多くは火災時に塗
膜にヒビ割れが生じたり脱落したりして延焼防止効果が
低下することがある。また、洞道などの狭い場所に布設
される電線・ケーブルに均一に塗装することが困難であ
り、場合によっては乾燥せず塗装後流動する恐れもある
。[Problems to be Solved by the Invention] In methods using fireproof paints, the coating film of many fireproof paints may crack or fall off in the event of a fire, reducing the fire spread prevention effect. In addition, it is difficult to uniformly coat electric wires and cables installed in narrow places such as tunnels, and in some cases, the coating may not dry and flow after coating.
防火テープあるいはシートの巻回による方法では、比較
的良好な延焼防止効果が達成されるが、難燃性が不十分
であり、十分な延焼防止効果が達成されない場合がある
。The method of winding a fireproof tape or sheet achieves a relatively good fire spread prevention effect, but the flame retardance is insufficient and a sufficient fire spread prevention effect may not be achieved.
本発明は、上記に基いたものでり、高い離燃性を付与て
きることから優れた耐火性能を発揮できる耐火組成物の
提供を目的とするものである。The present invention is based on the above, and aims to provide a fire-resistant composition that can exhibit excellent fire-resistant performance by imparting high flammability.
本発明の耐火組成物は、ポリクロロプレン100重量部
に対して炭化水素系多価アルコール80〜120重量部
および難燃性脱水剤80〜120重量部含有することを
特徴とするものである。The fireproof composition of the present invention is characterized by containing 80 to 120 parts by weight of a hydrocarbon polyhydric alcohol and 80 to 120 parts by weight of a flame retardant dehydrating agent based on 100 parts by weight of polychloroprene.
本発明において、ポリクロロプレンとしてはネオプレン
W1ネオプレンWRT、ネオプレンWB等の商品名で市
販されているものが使用でき、これらを適当な割合でブ
レンドして使用してもよい。In the present invention, as the polychloroprene, those commercially available under trade names such as Neoprene W1, Neoprene WRT, and Neoprene WB can be used, and these may be used by blending them in an appropriate ratio.
炭化水素系多価アルコールとしては、モノペンタエリス
リトール、ジペンタエリスリトール、ポリペンタエリス
リトール、ソルビトール等があげられる。Examples of the hydrocarbon polyhydric alcohol include monopentaerythritol, dipentaerythritol, polypentaerythritol, and sorbitol.
難燃性脱水剤は、熱分解して炭化水素系多価アルコール
に含まれているヒドロキシル基と反応して発泡炭化層を
形成するもので、りん酸アンモニウム、ポリりん酸アン
モニウム、りん酸メラミン等があげられる。Flame-retardant dehydrating agents are those that thermally decompose and react with the hydroxyl groups contained in hydrocarbon polyhydric alcohols to form a foamed carbonized layer, such as ammonium phosphate, ammonium polyphosphate, melamine phosphate, etc. can be given.
炭化水素系多価アルコールおよび難燃性脱水剤はそれぞ
れポリクロロプレン100重量部に対して80〜120
重量部の範囲で含有させる必要があり、80重量部未満
では難燃性および/または発泡炭化性が不十分であり、
120重量部を越えると混練加工性が著しく悪くなる。The amount of hydrocarbon polyhydric alcohol and flame retardant dehydrating agent is 80 to 120 parts by weight per 100 parts by weight of polychloroprene.
It is necessary to contain within a range of parts by weight, and if it is less than 80 parts by weight, flame retardancy and/or foaming carbonization properties are insufficient.
If it exceeds 120 parts by weight, kneading processability will be significantly impaired.
本発明においては、上記成分以外に通常ゴム、プラスチ
ックで使用される劣化防止剤、可塑剤、軟化剤、着色剤
、安定剤等を添加しても差支えない。In the present invention, in addition to the above-mentioned components, deterioration inhibitors, plasticizers, softeners, colorants, stabilizers, etc. commonly used in rubbers and plastics may be added.
なお、加硫剤を添加して耐火層を加硫させると、炎に当
っても全く発泡せず、発泡炭化反応の中間生成物が表面
からドリップする現象が生ずるので加硫剤の添加は避け
、非加硫状態としておく必要がある。In addition, if a vulcanizing agent is added to vulcanize the fireproof layer, it will not foam at all even when exposed to flame, and the intermediate product of the foaming carbonization reaction will drip from the surface, so avoid adding a vulcanizing agent. , it is necessary to keep it in an unvulcanized state.
本発明における耐火組成物は、電線・ケーブル等の可燃
生物の外周に直接押出被覆することにより耐火層を形成
できる。また、耐火組成物をテープあるいはシート状に
成形し、これを可燃性物に巻回するなどして耐火層を形
成することも可能である。The fire-resistant composition of the present invention can form a fire-resistant layer by directly extruding and coating the outer periphery of combustible objects such as electric wires and cables. It is also possible to form a fireproof layer by forming the fireproof composition into a tape or sheet and winding it around a combustible material.
[発明の実施例]
第1表の各側に示す配合の耐火組成物について、難燃性
、発泡炭化性、ロール混練性の各項目について評価し、
その結果を第2表の評価基準に従い第1表の下欄に示し
た。なお、評価は次に基いて行った。[Examples of the Invention] The fireproof compositions having the formulations shown on each side of Table 1 were evaluated for each item of flame retardancy, foaming carbonization property, and roll kneading property.
The results are shown in the lower column of Table 1 according to the evaluation criteria in Table 2. The evaluation was based on the following.
酸素指数:東洋理化工業(構製燃焼試験器0N−1型を
用いて測定した。Oxygen index: Measured using Toyo Rika Kogyo (structural combustion tester 0N-1 type).
発泡炭化性:添付図面に示すように、直径2mmの銅線
lに厚さ1 m mの架橋ポリエチレン絶縁体2を被覆
した絶縁電線3を用い、これに各側の耐火組成物を厚さ
5mmに押出被覆して耐火層4を形成して試料を作製し
た。この試料を実験用ブンゼンバーナー6で加熱し、架
橋ポリエチレン絶縁体2上に縦添えした直径0.4mm
の銅線5と銅線1との間の電気抵抗を絶縁抵抗計Ωで測
定し、電気抵抗が1MΩ以下となる時間により判定した
。電気抵抗の測定は、横河北辰電機(掬の電池式絶縁抵
抗計を用い、電圧は100OVとした。Foaming carbonization: As shown in the attached drawing, an insulated wire 3 is used, in which a copper wire 1 with a diameter of 2 mm is coated with a cross-linked polyethylene insulator 2 with a thickness of 1 mm, and a fire-resistant composition is coated on each side with a thickness of 5 mm. A sample was prepared by extrusion coating to form a fireproof layer 4. This sample was heated with an experimental Bunsen burner 6 and placed vertically on a cross-linked polyethylene insulator 2 with a diameter of 0.4 mm.
The electrical resistance between the copper wire 5 and the copper wire 1 was measured using an insulation resistance meter Ω, and the determination was made based on the time when the electrical resistance became 1 MΩ or less. The electrical resistance was measured using a battery-type insulation resistance meter manufactured by Yokogawa Hokushin Electric Co., Ltd. (Kiku), and the voltage was 100 OV.
ロール混練性二8インチ2本ロールでの混練作業性から
判定した。Roll kneading property It was judged from the kneading workability using two 28-inch rolls.
第 2 表
第1表からも明らかな通り、本発明の範囲にある実施例
ではいずれの評価項目においても十分満足できる結果と
なっている。これに対し、比較例1は炭化水素系多価ア
ルコールおよび難燃性脱水剤の含有量が規定値より少な
い場合であり、難燃性および発泡炭化性が劣った。比較
例2は炭化水素系多価アルコールの含有量が規定値より
少ない場合、比較3は難燃性脱水剤の含有量が規定値よ
り少ない場合であり、難燃性は良好であるが殆ど発泡せ
ず、加熱による中間生成物が表面からドリップする現象
がみられた。比較例4は炭化水素系多価アルコールおよ
び難燃性脱水剤の含有量が規定値より多い場合であり、
ロール混練作業性が著しく劣る。Table 2 As is clear from Table 1, the Examples within the scope of the present invention had sufficiently satisfactory results in all evaluation items. On the other hand, in Comparative Example 1, the contents of the hydrocarbon polyhydric alcohol and the flame retardant dehydrating agent were lower than the specified values, and the flame retardance and foaming carbonization were inferior. Comparative Example 2 is a case where the content of hydrocarbon polyhydric alcohol is less than the specified value, and Comparative Example 3 is a case where the content of the flame retardant dehydrating agent is less than the specified value, and although the flame retardance is good, there is almost no foaming. However, there was a phenomenon in which intermediate products caused by heating dripped from the surface. Comparative example 4 is a case where the content of hydrocarbon polyhydric alcohol and flame retardant dehydrating agent is higher than the specified value,
Roll kneading workability is extremely poor.
[発明の効果コ
以上説明してきた通り、本発明によれば、良好な難燃性
および耐火性能を有する耐火層の実現が可能となる。[Effects of the Invention] As explained above, according to the present invention, it is possible to realize a fireproof layer having good flame retardancy and fireproof performance.
添付図面は発泡炭化性の評価方法の説明図である。 The attached drawing is an explanatory diagram of a method for evaluating foaming carbonization property.
Claims (1)
系多価アルコール80〜120重量部および難燃性脱水
剤80〜120重量部含有することを特徴とする非加硫
性耐火組成物。(1) A non-vulcanizable fire-resistant composition containing 80 to 120 parts by weight of a hydrocarbon polyhydric alcohol and 80 to 120 parts by weight of a flame retardant dehydrating agent per 100 parts by weight of polychloroprene.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP22786586A JPS6383192A (en) | 1986-09-26 | 1986-09-26 | Fire-proof composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP22786586A JPS6383192A (en) | 1986-09-26 | 1986-09-26 | Fire-proof composition |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6383192A true JPS6383192A (en) | 1988-04-13 |
Family
ID=16867568
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP22786586A Pending JPS6383192A (en) | 1986-09-26 | 1986-09-26 | Fire-proof composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6383192A (en) |
-
1986
- 1986-09-26 JP JP22786586A patent/JPS6383192A/en active Pending
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