JPH02103252A - Flexible fluororesin composition - Google Patents
Flexible fluororesin compositionInfo
- Publication number
- JPH02103252A JPH02103252A JP25654788A JP25654788A JPH02103252A JP H02103252 A JPH02103252 A JP H02103252A JP 25654788 A JP25654788 A JP 25654788A JP 25654788 A JP25654788 A JP 25654788A JP H02103252 A JPH02103252 A JP H02103252A
- Authority
- JP
- Japan
- Prior art keywords
- tetrafluoroethylene
- parts
- propylene copolymer
- weight
- hydrogen fluoride
- 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 abstract description 18
- 229920001577 copolymer Polymers 0.000 claims abstract description 20
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims abstract description 15
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 claims abstract description 15
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 claims abstract description 12
- 229910000323 aluminium silicate Inorganic materials 0.000 claims abstract description 12
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims abstract description 12
- 229910000040 hydrogen fluoride Inorganic materials 0.000 claims abstract description 12
- 238000005979 thermal decomposition reaction Methods 0.000 claims abstract description 8
- 229920006172 Tetrafluoroethylene propylene Polymers 0.000 abstract description 6
- 239000002341 toxic gas Substances 0.000 abstract description 4
- 238000010292 electrical insulation Methods 0.000 abstract description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 abstract description 2
- 238000013329 compounding Methods 0.000 abstract 1
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 6
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 4
- KOMNUTZXSVSERR-UHFFFAOYSA-N 1,3,5-tris(prop-2-enyl)-1,3,5-triazinane-2,4,6-trione Chemical compound C=CCN1C(=O)N(CC=C)C(=O)N(CC=C)C1=O KOMNUTZXSVSERR-UHFFFAOYSA-N 0.000 description 3
- 235000021355 Stearic acid Nutrition 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000004132 cross linking Methods 0.000 description 3
- 239000000395 magnesium oxide Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 3
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 3
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 3
- 239000008117 stearic acid Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 239000010432 diamond Substances 0.000 description 2
- 229910003460 diamond Inorganic materials 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 230000002000 scavenging effect Effects 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- 239000005083 Zinc sulfide Substances 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
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000000370 acceptor Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- DNEHKUCSURWDGO-UHFFFAOYSA-N aluminum sodium Chemical compound [Na].[Al] DNEHKUCSURWDGO-UHFFFAOYSA-N 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 229910000410 antimony oxide Inorganic materials 0.000 description 1
- 150000004982 aromatic amines Chemical class 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
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 229910052593 corundum Inorganic materials 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 239000003431 cross linking reagent 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
- IQDXNHZDRQHKEF-UHFFFAOYSA-N dialuminum;dicalcium;dioxido(oxo)silane Chemical compound [Al+3].[Al+3].[Ca+2].[Ca+2].[O-][Si]([O-])=O.[O-][Si]([O-])=O.[O-][Si]([O-])=O.[O-][Si]([O-])=O.[O-][Si]([O-])=O IQDXNHZDRQHKEF-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 239000012784 inorganic fiber Substances 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 239000005078 molybdenum compound Substances 0.000 description 1
- 150000002752 molybdenum compounds Chemical class 0.000 description 1
- 210000003739 neck Anatomy 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920002620 polyvinyl fluoride Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910001845 yogo sapphire Inorganic materials 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Organic Insulating Materials (AREA)
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明は、四フッ化エチレン・プロピレン共重合の熱分
解で生じるフッ化水素を捕捉して火災時等に有毒ガスが
蔓延することを抑制した可撓性フッ素樹脂組成物に関す
る。[Detailed Description of the Invention] Industrial Application Field The present invention is a method for suppressing the spread of toxic gas in the event of a fire by capturing hydrogen fluoride generated by thermal decomposition of tetrafluoroethylene/propylene copolymer. The present invention relates to a flexible fluororesin composition.
従来の技術及び課題
四フッ化エチレン・プロピレン共重合体をペースに用い
た組成物は、可撓性、電気特性、耐熱性、難燃性などに
優れ、モータ用リード線や電子機器用配線等の種々の製
品における被覆材として多用されている。Conventional technologies and issues Compositions using tetrafluoroethylene/propylene copolymer as a paste have excellent flexibility, electrical properties, heat resistance, flame retardance, etc., and are used as lead wires for motors, wiring for electronic devices, etc. It is widely used as a coating material in various products.
し7かしながら、四フッ化エチレン・プロピレン共重合
体は、火災時等における熱分解で有毒なフッ化水素を発
生する問題点がある。However, the tetrafluoroethylene/propylene copolymer has the problem of generating toxic hydrogen fluoride when thermally decomposed during a fire or the like.
課題を解決するための手段
本発明は、含水アルミノケイ酸塩を配合して上記の問題
点を克服したものである。Means for Solving the Problems The present invention overcomes the above problems by incorporating a hydrous aluminosilicate.
すなわち、本発明は、四フッ化エチレン・プロピレン共
重合体を成分とする可撓性組成物に、四フッ化エチレン
・プロピレン共重合体100重量部あたり15〜170
重量部の含水アルミノケイ酸塩を配合して、四フッ化エ
チレン・プロピレン共重合体の熱分解で生じるフッ化水
素の捕捉能を付与したことを特徴とする可撓性フッ素制
脂組成物を提供するものである。That is, the present invention provides a flexible composition containing a tetrafluoroethylene/propylene copolymer with 15 to 170 parts by weight per 100 parts by weight of the tetrafluoroethylene/propylene copolymer.
Provided is a flexible fluorinated antigreasing composition, characterized in that it contains part by weight of hydrated aluminosilicate to impart the ability to capture hydrogen fluoride generated by thermal decomposition of tetrafluoroethylene/propylene copolymer. It is something to do.
作 用
含水アルミノケイ酸塩を配合することにより、可撓性、
電気特性、耐熱性、難燃性等の物性を推持しつつ、火災
時等における熱分解で発生したフッ化水素等の有毒カス
を捕捉して、それが拡散したり、蔓延することを抑制す
ることができる。Function By blending hydrated aluminosilicate, flexibility and
While maintaining physical properties such as electrical properties, heat resistance, and flame retardancy, it captures toxic residue such as hydrogen fluoride generated by thermal decomposition during fires, etc., and suppresses its diffusion and spread. can do.
発明の構成要素の例示
本発明の組成物は、四フッ化エヂレン・プロピレン共重
合体を用いて可撓性をもたせたものである。その種類に
つき特に限定はない。エチレン・四フッ化エチレン、フ
ッ化エチレン・プロピレン共重合体、ポリフッ化ビニル
、フッ素ゴムグラフト化フッ素樹脂の如きポリマ成分を
通例、四フッ化エチレン・プロピレン共重合体100重
量部あたり25重量部以下併用して、機械的強度を向上
さぜたもの、フッ素樹脂の粉末や無機繊維を通例、四フ
ッ化エチレン・プロピレン共重合体100重量部あたり
5〜70重量部配合して引裂き強度を向上させたもの、
有機過酸化物等の架橋剤や、アリル化合物、イオ「り、
マレイミド、オキシム類等の架橋助剤を配合して水蒸気
架橋等を施しうるようにしたものなとが代表例としてあ
げられる。その他、水和アルミナ、水和マグネシウム、
炭酸マグネシウム、酸化アンチモン、赤リン、モリブデ
ン化合物、ホウ酸化合物、デカブロモジフェニルオキシ
ドの如き難燃剤、カーボンブラック、タルク、硫酸バリ
ウム、水酸化アルミニウム、クレー、シリカ、炭酸カル
シウム、硫化亜鉛、酸化亜鉛の如き充填剤、ステアリン
酸、ステアリン酸ソーダの如き滑剤、酸化マグネシウム
、水酸化カルシウムの如き受酸剤、イミダゾール類、ケ
トン−アミン縮合物類、フェノール類、ヒンダードフェ
ノール頚、芳香族アミン類の如き老化防止剤、酸化チタ
ン、フタロシアニンブルー、ベンガラの如き顔料、チタ
ネート系、アルミニウム系、シラン系等のカップリング
剤、ステアリン酸、オレイン酸、高級脂肪酸金属塩の如
き滑剤、加工助剤などで代表される、ゴムやプラスチッ
クに添加されることのある添加剤が必要に応じ配合され
たものなどもあげられる。Exemplification of Constituent Elements of the Invention The composition of the present invention is made flexible using a tetrafluoroethylene propylene copolymer. There are no particular limitations on the type. Polymer components such as ethylene/tetrafluoroethylene, fluorinated ethylene/propylene copolymer, polyvinyl fluoride, and fluororubber-grafted fluororesin are usually 25 parts by weight or less per 100 parts by weight of tetrafluoroethylene/propylene copolymer. When used in combination with materials that improve mechanical strength, fluororesin powder or inorganic fibers are usually added in an amount of 5 to 70 parts by weight per 100 parts by weight of tetrafluoroethylene/propylene copolymer to improve tear strength. things,
Crosslinking agents such as organic peroxides, allyl compounds, iodine, etc.
Typical examples include those in which crosslinking aids such as maleimide and oximes are blended to enable steam crosslinking. Others include hydrated alumina, hydrated magnesium,
Magnesium carbonate, antimony oxide, red phosphorus, molybdenum compounds, boric acid compounds, flame retardants such as decabromodiphenyl oxide, carbon black, talc, barium sulfate, aluminum hydroxide, clay, silica, calcium carbonate, zinc sulfide, zinc oxide. Fillers such as stearic acid, lubricants such as stearic acid and sodium stearate, acid acceptors such as magnesium oxide and calcium hydroxide, imidazoles, ketone-amine condensates, phenols, hindered phenol necks, and aromatic amines. Typical examples include anti-aging agents, pigments such as titanium oxide, phthalocyanine blue, and red iron, coupling agents such as titanate, aluminum, and silane, lubricants such as stearic acid, oleic acid, and higher fatty acid metal salts, and processing aids. Examples include those that contain additives that are sometimes added to rubber and plastics, as necessary.
なお、電気絶縁性の点よりは、四フッ化エチレン/プロ
ピレンのモル比が55/45で、ムーニー粘度(100
℃)が30〜150の四フッ化エチレン・プロピレン共
重合体を用いたものが好ましい。また、架橋処理は電子
線等を照射する方式によっても行いつる。In addition, from the point of view of electrical insulation, the molar ratio of tetrafluoroethylene/propylene is 55/45, and the Mooney viscosity (100
It is preferable to use a tetrafluoroethylene/propylene copolymer having a temperature (°C) of 30 to 150. Further, the crosslinking treatment can also be carried out by irradiating with an electron beam or the like.
本発明の組成物は、含水アルミノケイ酸塩を配合して捕
捉能を付与したものである。捕捉の対象は、火災時等の
熱分解で生じるガス、特に四フッ化エヂレン・プロピレ
ン共重合体の熱分解で生じるフッ化水素等の有毒ガスで
ある。The composition of the present invention contains a hydrous aluminosilicate to impart scavenging ability. The targets to be captured are gases generated during thermal decomposition during fires, particularly toxic gases such as hydrogen fluoride generated during thermal decomposition of tetrafluoroethylene propylene copolymer.
用いる含水アルミノケイ酸塩は、一般式:%式%
(ただし、Mはアルカリ金属又はアルカリ土類金属で、
Xはその原子価であり、e、、m1nは任意な数である
。)で表される立体網状構造を有するものであり、ゼオ
ライト(商品名)などの市販品がある。天然物及び合成
物のいずれの含水アルミノケイ酸塩も用いることができ
る。変色防止性、耐候性、電気特性の点より合成ケイ酸
アルミニウムツノルシウム(CaO・Al2O3・2S
IO24H20)が好ましく用いられる。The hydrated aluminosilicate to be used has the general formula: % formula % (where M is an alkali metal or alkaline earth metal,
X is its valence, and e, , m1n are arbitrary numbers. ), and there are commercially available products such as Zeolite (trade name). Both natural and synthetic hydrated aluminosilicates can be used. Synthetic aluminum silicate (CaO・Al2O3・2S
IO24H20) is preferably used.
含水アルミノケイ酸塩の配合量は、四フッ化エチレン・
プロピレン共重合体100重量部あたり15〜170重
量部が適当であり、好ましくは30〜150重量部、特
に好ましくは30〜100重量部である。その配合量が
15重量部未満では捕捉能に乏しいし、170重量部を
超えると実用に耐える機械的物11を有する組成物が得
られない。The amount of hydrated aluminosilicate is
A suitable amount is 15 to 170 parts by weight, preferably 30 to 150 parts by weight, particularly preferably 30 to 100 parts by weight, per 100 parts by weight of the propylene copolymer. If the amount is less than 15 parts by weight, the scavenging ability will be poor, and if it exceeds 170 parts by weight, a composition having mechanical properties 11 that can withstand practical use cannot be obtained.
本発明の組成物は、配合する各成分を混合することによ
り調製される。混合はロールミル、バンバリーミキサ、
ヘンシェルミキサなどの適宜な混合機を用いて行ってよ
い。その際、2種以上のボノマ成分を併用する場合には
、含水アルミノケイ酸塩が100℃以上では少量の水を
放出するおそれがあるので、それらを予め混合しておく
ことが好ましい。The composition of the present invention is prepared by mixing the respective components to be blended. Mixing is done using a roll mill, Banbury mixer,
This may be carried out using a suitable mixer such as a Henschel mixer. In this case, when two or more types of bonoma components are used together, it is preferable to mix them in advance, since there is a risk that the hydrated aluminosilicate may release a small amount of water at 100° C. or higher.
本発明の組成物は、そのまま電線の絶縁材や各種物品の
被覆材、あるいはシート製品など、種々の用途に用いる
ことができる。また、例えばエチレン・プロピレン共重
合体など他の被覆材等の改質剤などとしても用いること
ができる。The composition of the present invention can be used as it is for various purposes such as insulating materials for electric wires, coating materials for various articles, and sheet products. It can also be used as a modifier for other coating materials such as ethylene-propylene copolymers.
発明の効果
本発明によれば、含水アルミノケイ酸塩を配合したので
、四フッ化エチレン・プロピレン共重合体の可撓性、電
気特性、耐熱性、難燃性を良好に維持したまま、四フッ
化エチレン・プロピレン共重合体の熱分解で生じるフッ
化水素の拡散、ないし蔓延を抑制することができる。ま
た、その他の有毒ガスも捕捉することができ、公害防止
力ないし安全性に優れている。Effects of the Invention According to the present invention, since a hydrous aluminosilicate is blended, the flexibility, electrical properties, heat resistance, and flame retardance of the tetrafluoroethylene/propylene copolymer are maintained well. It is possible to suppress the diffusion or spread of hydrogen fluoride generated by thermal decomposition of the ethylene/propylene copolymer. In addition, it can also capture other toxic gases, providing excellent pollution prevention and safety.
実施例
実施例1
アフラス150E(商品名、旭硝子社製;四)・ソ化エ
チレン・プロピレン共重合体)100部(重量部、以下
同じ)、ステアリン酸ナトリウム2部、マグネシア3部
、ダイヤブラックH(商品名、三菱モンザント社製;カ
ーボンブラック)5部、C5−100(商品名、耕正社
製;合成ケイ酸アルミニウムノ1ルシウム)30部、パ
ークミルD(商品名、日本油脂社製;ジクミルパーオキ
シド)2部及びTAIC(商品名、日本化成社製;トリ
アリルイソシアネート)5部を、2本ロールを用いて常
温で混練したのち、その混合物を170℃で20分間の
条件でプレス架橋し、厚さ2Mの架橋シートを得た。Examples Example 1 Aflas 150E (trade name, manufactured by Asahi Glass Co., Ltd.; 4), 100 parts (parts by weight, same hereinafter) of sonicated ethylene propylene copolymer), 2 parts of sodium stearate, 3 parts of magnesia, Diamond Black H (Product name, manufactured by Mitsubishi Monzanto Corporation; Carbon Black) 5 parts, C5-100 (Product name, manufactured by Kosei Co., Ltd.; synthetic aluminum lucium silicate) 30 parts, Percmill D (Product name, manufactured by NOF Corporation; After kneading 2 parts of TAIC (trade name, Nippon Kasei Co., Ltd.; triallyl isocyanate) at room temperature using two rolls, the mixture was press-crosslinked at 170°C for 20 minutes. A crosslinked sheet with a thickness of 2M was obtained.
実施例2
C3−100の使用量を60部としたほかは実施例1に
準じて架橋シートを得た。Example 2 A crosslinked sheet was obtained according to Example 1 except that the amount of C3-100 used was 60 parts.
実施例3
C3−100の使用量を120部としたほかは実施例1
に準じて架橋シートを得た。Example 3 Example 1 except that the amount of C3-100 used was 120 parts.
A crosslinked sheet was obtained according to .
実施例4
C8−100に代えてC8−500(商品名、耕正社製
;合成ケイ酸アルミニウムカルシウム)を用いたほかは
実施例2に準じて架橋シートを得た。Example 4 A crosslinked sheet was obtained according to Example 2, except that C8-500 (trade name, manufactured by Kosei Co., Ltd.; synthetic aluminum calcium silicate) was used in place of C8-100.
実施例5
C8−100に代えてSP#2300 (商品名、日東
粉化社製;天然ケイ酸アルミニウムナトリウム)を用い
たほかは実施例2に準じて架橋シートを得た。Example 5 A crosslinked sheet was obtained according to Example 2, except that SP#2300 (trade name, manufactured by Nitto Funka Co., Ltd.; natural sodium aluminum silicate) was used in place of C8-100.
実施例6
アララス150E;80部と、セフラルソフトG−15
0(商品名、セントラル硝子社製;フッ素ゴムグラフト
化フッ素樹脂)20部を170〜180℃で20分間充
分に混練し、その混合物にステアリン酸ナトリウム2部
、マグネシア3部、ダイヤ1972825部、C5−1
00;60部、パークミルD:2部及びTAIC;5部
を加え、2本ロールを用いて常温て混練した。ついで、
その混合物を170℃で20分間の条件でプレス架橋し
、厚さ2mの架橋シートを得た。Example 6 Araras 150E; 80 parts and Cefural Soft G-15
0 (trade name, manufactured by Central Glass Co., Ltd.; fluorine rubber-grafted fluororesin) were thoroughly kneaded at 170 to 180°C for 20 minutes, and to the mixture were added 2 parts of sodium stearate, 3 parts of magnesia, 1,972,825 parts of diamond, and C5. -1
60 parts of Percmill D, 2 parts of TAIC, and 5 parts of TAIC were added and kneaded at room temperature using two rolls. Then,
The mixture was press crosslinked at 170° C. for 20 minutes to obtain a crosslinked sheet with a thickness of 2 m.
実施例7
アフラス150Eの使用量を90部とし、セフラルソフ
1−G−150;20部に代えてアフロンCOP C
55A(商品名、旭硝子社製;エチレン・四フッ化エチ
レン共重合体)10部を用いたほかは実施例6に準じて
架橋シートを得た。Example 7 The amount used of Afrons 150E was 90 parts, and Cefrarusof 1-G-150 was replaced with 20 parts by Aphron COP C.
A crosslinked sheet was obtained in accordance with Example 6, except that 10 parts of 55A (trade name, manufactured by Asahi Glass Co., Ltd.; ethylene/tetrafluoroethylene copolymer) was used.
実施例8
C5−100の使用量を50部とし、硫酸バリウム10
部を追加配合たほかは実施例2に準じて架橋シートを得
た。Example 8 The amount of C5-100 used was 50 parts, and barium sulfate 10
A crosslinked sheet was obtained in the same manner as in Example 2, except that the following procedure was performed:
比較例I
C3−100を配合せず、硫酸バリウムの使用量を30
部としたほかは実施例8に準じて架橋シートを得た。Comparative Example I C3-100 was not blended and the amount of barium sulfate used was 30
A crosslinked sheet was obtained according to Example 8 except that
比較例2
C8−100の使用量を200部としたほかは実施例1
に準じ架橋シートを得た。Comparative Example 2 Example 1 except that the amount of C8-100 used was 200 parts.
A crosslinked sheet was obtained according to .
評価試験
実施例、比較例で得た架橋シートにつき下記の試験を行
った。The following tests were conducted on the crosslinked sheets obtained in the evaluation test examples and comparative examples.
[引張強さ、伸び]
JIS K 6301の引張試験方法に準拠して破断
時の引張強さ、及び伸びを調べた。[Tensile Strength, Elongation] The tensile strength and elongation at break were examined in accordance with the tensile test method of JIS K 6301.
[フッ化水素発生量]
JC853(日本電線工業会規格)における塩酸ガス測
定法に準拠して、組成物を800℃で30分間強熱し、
発生したフッ化水素をN15水酸化す1ヘリウム溶液に
吸収させた。ついで、得られた吸収液をJIS K
0105 (排ガス中のフッ素化合物の分析方法)にお
けるイオン電極法に準じてフッ化水素量を測定した。[Amount of Hydrogen Fluoride Generated] The composition was ignited at 800°C for 30 minutes in accordance with the hydrochloric acid gas measurement method in JC853 (Japan Electric Cable Manufacturers Association standard),
The generated hydrogen fluoride was absorbed into a N15 hydroxide/1 helium solution. Then, the obtained absorption liquid was rated according to JIS K
The amount of hydrogen fluoride was measured according to the ion electrode method in 0105 (Method for analyzing fluorine compounds in exhaust gas).
表より、実施例ではフッ化水素の発生量が少なく、シか
も引張強さ及び伸びを良好に維持していることがわかる
。From the table, it can be seen that in the examples, the amount of hydrogen fluoride generated was small, and the tensile strength and elongation were maintained well.
特許出願人 三菱電線工業株式会社Patent applicant: Mitsubishi Cable Industries, Ltd.
Claims (1)
る可撓性組成物に、四フッ化エチレン・プロピレン共重
合体100重量部あたり15〜170重量部の含水アル
ミノケイ酸塩を配合して、四フッ化エチレン・プロピレ
ン共重合体の熱分解で生じるフッ化水素の捕捉能を付与
したことを特徴とする可撓性フッ素樹脂組成物。1. A flexible composition containing tetrafluoroethylene/propylene copolymer is blended with 15 to 170 parts by weight of hydrated aluminosilicate per 100 parts by weight of tetrafluoroethylene/propylene copolymer. A flexible fluororesin composition characterized by being endowed with the ability to capture hydrogen fluoride generated by thermal decomposition of an ethylene-propylene copolymer.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP25654788A JPH02103252A (en) | 1988-10-12 | 1988-10-12 | Flexible fluororesin composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP25654788A JPH02103252A (en) | 1988-10-12 | 1988-10-12 | Flexible fluororesin composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH02103252A true JPH02103252A (en) | 1990-04-16 |
Family
ID=17294155
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP25654788A Pending JPH02103252A (en) | 1988-10-12 | 1988-10-12 | Flexible fluororesin composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH02103252A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010071717A (en) * | 2008-09-17 | 2010-04-02 | Fuji Electric Holdings Co Ltd | Method and apparatus for analyzing non-condensible gas of refrigerant |
| CN102131545A (en) * | 2006-03-20 | 2011-07-20 | 塞拉莫普泰克工业公司 | Device and method for treating benign prostatic hyperplasia |
-
1988
- 1988-10-12 JP JP25654788A patent/JPH02103252A/en active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102131545A (en) * | 2006-03-20 | 2011-07-20 | 塞拉莫普泰克工业公司 | Device and method for treating benign prostatic hyperplasia |
| JP2010071717A (en) * | 2008-09-17 | 2010-04-02 | Fuji Electric Holdings Co Ltd | Method and apparatus for analyzing non-condensible gas of refrigerant |
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