JPS62167339A - Flame-retardant resin composition - Google Patents
Flame-retardant resin compositionInfo
- Publication number
- JPS62167339A JPS62167339A JP797486A JP797486A JPS62167339A JP S62167339 A JPS62167339 A JP S62167339A JP 797486 A JP797486 A JP 797486A JP 797486 A JP797486 A JP 797486A JP S62167339 A JPS62167339 A JP S62167339A
- Authority
- JP
- Japan
- Prior art keywords
- olefin
- flame
- magnesium hydroxide
- resin composition
- groups
- 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
- 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 title claims description 13
- 239000003063 flame retardant Substances 0.000 title claims description 13
- 239000011342 resin composition Substances 0.000 title claims description 9
- 239000004711 α-olefin Substances 0.000 claims abstract description 14
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 13
- 239000000194 fatty acid Substances 0.000 claims abstract description 13
- 229930195729 fatty acid Natural products 0.000 claims abstract description 13
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 13
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 claims abstract description 12
- 239000000347 magnesium hydroxide Substances 0.000 claims abstract description 12
- 229910001862 magnesium hydroxide Inorganic materials 0.000 claims abstract description 12
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 6
- 229920000089 Cyclic olefin copolymer Polymers 0.000 claims abstract description 5
- 239000006087 Silane Coupling Agent Substances 0.000 claims abstract description 5
- 150000003839 salts Chemical class 0.000 claims abstract description 5
- 229910052751 metal Inorganic materials 0.000 claims description 9
- 239000002184 metal Substances 0.000 claims description 9
- 229920005989 resin Polymers 0.000 claims description 9
- 239000011347 resin Substances 0.000 claims description 9
- 150000001336 alkenes Chemical class 0.000 claims description 5
- 229920001519 homopolymer Polymers 0.000 claims description 5
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 3
- 239000000203 mixture Substances 0.000 abstract description 11
- -1 polyethylene Polymers 0.000 abstract description 6
- 238000004381 surface treatment Methods 0.000 abstract description 4
- 229920001400 block copolymer Polymers 0.000 abstract description 3
- 238000002485 combustion reaction Methods 0.000 abstract description 3
- 230000005484 gravity Effects 0.000 abstract description 3
- 238000002156 mixing Methods 0.000 abstract description 2
- 239000004698 Polyethylene Substances 0.000 abstract 1
- 231100000614 poison Toxicity 0.000 abstract 1
- 230000007096 poisonous effect Effects 0.000 abstract 1
- 229920000573 polyethylene Polymers 0.000 abstract 1
- 239000007789 gas Substances 0.000 description 10
- 238000000034 method Methods 0.000 description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- 229910052736 halogen Inorganic materials 0.000 description 4
- 150000002367 halogens Chemical class 0.000 description 4
- 239000004677 Nylon Substances 0.000 description 3
- 239000004793 Polystyrene Substances 0.000 description 3
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 3
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 3
- 229920001778 nylon Polymers 0.000 description 3
- 229920000098 polyolefin Polymers 0.000 description 3
- 229920002223 polystyrene Polymers 0.000 description 3
- 229920005604 random copolymer Polymers 0.000 description 3
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 125000003700 epoxy group Chemical group 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 150000002736 metal compounds Chemical class 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 125000000962 organic group Chemical group 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 229920005992 thermoplastic resin Polymers 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical group CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 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
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene 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
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical group CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 125000003709 fluoroalkyl group Chemical group 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- 150000002366 halogen compounds Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 238000009413 insulation Methods 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
- 239000000314 lubricant Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000008188 pellet Substances 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
- 238000005498 polishing Methods 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229940096992 potassium oleate Drugs 0.000 description 1
- MLICVSDCCDDWMD-KVVVOXFISA-M potassium;(z)-octadec-9-enoate Chemical compound [K+].CCCCCCCC\C=C/CCCCCCCC([O-])=O MLICVSDCCDDWMD-KVVVOXFISA-M 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000012756 surface treatment agent Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 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、難燃性に優れ、燃焼時にあけるドリップ防止
およびノンハロゲン系の腐蝕性、有害性ガスの発生せず
、機械物性のバランスのとれ、更には押出加工性に優れ
た密度が0.92以下のα−オレフィンの単独重合体又
はその共重合体を使用したオレフィン系離燃性樹脂組成
物に関するものである。Detailed Description of the Invention (Field of Industrial Application) The present invention has excellent flame retardancy, prevents dripping during combustion, is non-halogen-based, corrosive, does not generate harmful gases, and has well-balanced mechanical properties. Furthermore, the present invention relates to an olefin-based flame retardant resin composition using an α-olefin homopolymer or copolymer thereof having a density of 0.92 or less and having excellent extrusion processability.
従来、電線、ケーブルをはじめ電器製品の絶縁材料とし
て多用されているポリオレフィン組成物に難燃性を付与
するためには、ポリオレフィンにハロゲン化合物と三酸
化アンチモンを添加することにより達成されていた。し
かるにこれらの組成物はハロゲン化合物であり燃焼時に
ハロゲン化ガスを発生するので人体に有害でおり、かつ
全屈が腐蝕されるので好ましくなかった。Conventionally, flame retardancy has been achieved in polyolefin compositions, which are often used as insulating materials for electric wires, cables, and other electrical appliances, by adding halogen compounds and antimony trioxide to polyolefins. However, these compositions are halogenated compounds and emit halogenated gas when burned, which is harmful to the human body and corrodes the entire bend, which is not desirable.
一方、従来の難燃性組成物におっては、難燃性は水和金
属化合物でノンハロゲン化を達成しているものの、ベー
スになる樹脂については、特許第1231199 @に
みられるように結晶状オレフィン単合体樹脂の他に、ポ
リスチレン、ABS、ナイロン等の熱可塑性樹脂をあげ
ているものが多くこれら樹脂の燃焼した場合のスチレン
系、アミド系が発生するノンハロゲンではあるが相当量
の有害ガスを発生する片手落らのところがみられた。On the other hand, in conventional flame retardant compositions, flame retardancy is achieved by non-halogenated hydrated metal compounds, but the base resin is crystalline as seen in Patent No. 1231199 @. In addition to olefin monopolymer resins, there are many that list thermoplastic resins such as polystyrene, ABS, and nylon, and when these resins are burned, they generate styrene and amide resins, which are non-halogen, but emit a considerable amount of harmful gas. The area where one hand fell off was seen.
また更に上記特許第1231199号にみられるように
熱可塑性樹脂、水酸化マグネシウムおよび炭素粉末の三
者による難燃向上を主体とした、自消性樹脂組成物は用
途によっては、特に通信線の絶縁線およびジャケットな
どは、多色、例えば8色などのカラー表示を限定されて
おり、炭素粉末によって難燃性向上を目的とした組成物
は、全く実際にそぐわない組成物があった。Furthermore, as seen in the above-mentioned Patent No. 1231199, self-extinguishing resin compositions mainly consisting of thermoplastic resin, magnesium hydroxide, and carbon powder to improve flame retardancy can be used for some applications, especially for insulation of communication lines. Lines, jackets, and the like are limited to multiple colors, for example, eight colors, and some compositions that aim to improve flame retardancy using carbon powder are completely unsuitable for actual use.
本発明は、前記の事情を考慮して成されたもので、その
目的とするところは、火災発生時の人体への安全性を高
く周囲の金属等を腐蝕させることもない、ノンハロゲン
ガスも元より有害ガスを全く発生しない、クリーンな無
公害化を達成したものである。The present invention has been made in consideration of the above circumstances, and its purpose is to provide a gas that is highly safe to the human body in the event of a fire, does not corrode surrounding metals, and is a non-halogen gas. It is a clean and non-polluting system that does not emit any harmful gases.
即ち、本発明は、ポリスチレン、ABS、ナイロン等の
有害ガスを発生する樹脂を対象外として、α−オレフィ
ン単独重合体およびα−オレフィンの共重合体を使用し
、しかもカーボンブラック等の炭素粉末を使用すること
を目的とせず、用途に応じて自由自在にカラーリングが
可能であり、さらには樹脂密度を0.92以下の低結晶
性の柔軟なものを使用し、1種以上のシランカップリン
グ剤などで表面処理された水酸化マグネシウムを使用す
ることにより、多量の水和金属を充填しても、非常に柔
軟で低温特性、および加工性に優れ、従来の炭素粉末の
添加での難燃性効果以上の多量の水和金属化合物を充填
できる難燃樹脂組成物を提供することにある。That is, the present invention excludes resins that generate harmful gases such as polystyrene, ABS, and nylon, and uses α-olefin homopolymers and α-olefin copolymers, and carbon powder such as carbon black. It is not intended for use, and can be freely colored according to the purpose, and furthermore, it uses a low-crystalline flexible material with a resin density of 0.92 or less, and one or more types of silane coupling. By using magnesium hydroxide that has been surface-treated with a chemical agent, it has excellent flexibility, low-temperature properties, and processability even when filled with a large amount of hydrated metal, and is flame retardant compared to the conventional addition of carbon powder. The object of the present invention is to provide a flame-retardant resin composition that can be filled with a large amount of a hydrated metal compound that has a superior performance effect.
本発明の難燃性樹脂組成物は、いずれもハロゲン元素を
一切含まず、燃焼しても有害性ガスを全く発生せず、樹
脂組成物の自由に着色化が容易であることを特徴とする
ものでおる。The flame-retardant resin compositions of the present invention are characterized in that they do not contain any halogen elements, do not generate any harmful gases even when burned, and are easy to freely color the resin composition. It's something.
(1)本発明において用いられるα−オレフィンの単独
重合体又は共重合体は、エチレン、プロピレン等のα−
オレフィンの単独重合体又は、α−オレフィンと他のα
−オレフィンとの結晶性のブロック又はランダム共重合
体例えば、結晶性プロピレン−エチレンブロック共重合
体、エチレン−ブテン−1ランダム共重合体、プロピレ
ン−ブテン−1ランダム共重合体、又は、α−オレフィ
ンを主体とする、酢酸ビニル、無水マレイン酸、アクリ
ル酸等の極性モノマーとの共重合体(グラフト共重合体
を含む)およびこれらの混合物であり、その比重が0.
92以下のものである。(1) The α-olefin homopolymer or copolymer used in the present invention is an α-olefin such as ethylene or propylene.
Homopolymers of olefins or α-olefins and other α-olefins
- crystalline block or random copolymers with olefins, such as crystalline propylene-ethylene block copolymers, ethylene-butene-1 random copolymers, propylene-butene-1 random copolymers, or α-olefins; copolymers (including graft copolymers) with polar monomers such as vinyl acetate, maleic anhydride, and acrylic acid, and mixtures thereof, whose specific gravity is 0.
92 or less.
これら混合物の組み合わせは樹脂組成物の表面硬度、耐
寒性、耐ストレスクラッキング、接着性向上などの諸々
の要求により組み合わせが可能であり、いずれの組み合
わせも容易に混練溶融される。Combinations of these mixtures can be made depending on various requirements such as improving the surface hardness, cold resistance, stress cracking resistance, and adhesion of the resin composition, and any combination can be easily kneaded and melted.
(2)本発明において使用される水酸化マグネシウムは
、シランカップリング剤シリコーン誘導体又は脂肪酸、
脂肪酸金属塩で表面処理を施したものを用いる。(2) Magnesium hydroxide used in the present invention is a silane coupling agent silicone derivative or a fatty acid,
Use one that has been surface-treated with a fatty acid metal salt.
(i)シランカップリング剤としては分子内の一方の末
端に無機質と反応する反応基(メトキシ基、エトキシ基
、カルボキシル基、セロソルブ基など)でおり、これは
一般的に三官能基を有する場合が多いが、三官能、−官
能を有する場合でももちろんよい。またもう一方の末端
には、有機材料である樹脂側と化学結合する反応基(ビ
ニル基、エポキシ基、メタクリル基、アミノ基、メルカ
プト基など)を有するもので主鎖がフルコキシオリゴマ
ーを骨格とするものである。(i) A silane coupling agent has a reactive group (methoxy group, ethoxy group, carboxyl group, cellosolve group, etc.) that reacts with an inorganic substance at one end of the molecule, and this generally has a trifunctional group. However, it is of course also possible to have trifunctional or -functional functional groups. In addition, the other end has a reactive group (vinyl group, epoxy group, methacrylic group, amino group, mercapto group, etc.) that chemically bonds with the resin side of the organic material, and the main chain has a flukoxy oligomer skeleton. It is something to do.
(11)シリコーン誘導体としては、ジメチルポリシロ
キサンのメチル基の一部を各種の有機基を置換したタイ
プで、各種の変性有機基としては、α−メチルスチレン
基、α−オレフィン基、ポリエーテル基、アルコール基
、フルオロアルキル基なとの相溶性、親水性、潤滑性、
祁水性などを改良することを目的とする変性基、アミン
基メルカプル基、エポキシ基、カルボキシル基などの反
応性、吸着性を目的とした変成基、高級脂肪酸、カルバ
ナ、アミドを置換した離型、つや出しを目的とした変成
基、メタアクリロキシプロピル基を有する反応性に富ん
だ変成型、末端にOH基、NH2基を有する反応型など
、多種多様の変成基を置換して導入したシリコーン変成
誘導体があげられる。(11) The silicone derivative is a type in which a part of the methyl group of dimethylpolysiloxane is substituted with various organic groups, and the various modified organic groups include α-methylstyrene group, α-olefin group, and polyether group. , compatibility with alcohol groups, fluoroalkyl groups, hydrophilicity, lubricity,
Modified groups for the purpose of improving water repellency, etc., modified groups for the purpose of reactivity and adsorption such as amine groups, mercapuru groups, epoxy groups, carboxyl groups, mold release substituted with higher fatty acids, carbana, and amide; Silicone modified derivatives introduced by substitution with a wide variety of modified groups, including modified groups for the purpose of polishing, highly reactive modified types with methacryloxypropyl groups, and reactive types with OH groups and NH2 groups at the terminals. can be given.
(iii)脂肪酸としては飽和および不飽和脂肪酸があ
り、炭素数が6以上22までの脂肪酸を指すが特に01
8のステアリン酸、オレイン酸があげられる。(iii) Fatty acids include saturated and unsaturated fatty acids, and refers to fatty acids with carbon numbers of 6 to 22, especially 01
Examples include stearic acid and oleic acid.
(iV)脂肪酸金属塩としては、上記の脂肪酸が金属と
結合した金属石けんを示し、特にステアリン酸ソーダ、
オレイン酸カリ、などがあげられる。(iv) Fatty acid metal salts include metal soaps in which the above-mentioned fatty acids are bonded to metals, particularly sodium stearate,
Examples include potassium oleate.
もちろん脂肪酸としては直鎖飽和型、不飽和型を問わず
側鎖部分が金属と結合したものも、もちろん有効である
。Of course, fatty acids with a side chain bonded to a metal are also effective, regardless of whether they are linear saturated or unsaturated.
上記(i)〜(iV)によって又はその混合体によって
表面処理された水酸化マグネシウムを50重優品から2
50重1部で連用した場合、低密度の低結晶性ポリマー
と相溶するか又は反応し高充填した場合でも容易に、低
温特性、柔軟性および加工性の優れた難燃組成物を形成
できるものであるが、50重量部以下ではその難燃効果
は著しく低下してしまう。また250重量部以上では、
難燃性が著しく向上するものの、柔軟性、低温特性等の
機械特性が低下し、加工性が極端に悪くなることを確認
している。Magnesium hydroxide surface-treated by the above (i) to (iV) or a mixture thereof, from 50 to 2
When used continuously at 50 parts by weight, it is compatible with or reacts with low-density, low-crystalline polymers, and can easily form flame-retardant compositions with excellent low-temperature properties, flexibility, and processability even when highly loaded. However, if the amount is less than 50 parts by weight, the flame retardant effect will be significantly reduced. In addition, at 250 parts by weight or more,
It has been confirmed that although flame retardancy is significantly improved, mechanical properties such as flexibility and low-temperature properties are reduced, and workability is extremely poor.
(3)他の添加物
本発明の難燃樹脂組成物は所望により、酸化防止剤、中
和剤、紫外線吸収剤、帯電防止剤、顔料、分散剤、滑剤
、増粘剤等の通常配合されるものは配合することができ
る。(3) Other additives The flame retardant resin composition of the present invention may contain antioxidants, neutralizers, ultraviolet absorbers, antistatic agents, pigments, dispersants, lubricants, thickeners, etc., if desired. can be blended.
(4)表面処理方法
処理方法は、ヘンシェルミキサー、ブレダー等の攪拌機
械で充分であり、機種によっては、処理の攪拌時間の長
短の差はあるものの、特別の装置を必要としない。(4) Surface treatment method A stirring machine such as a Henschel mixer or a blender is sufficient for the treatment method, and no special equipment is required, although the length of stirring time for treatment may vary depending on the model.
添加の方法は、滴下式、一括投入方式など、処理剤の使
用方法について使い分ける必要がある。It is necessary to use a different method of addition depending on how the processing agent is used, such as a dripping method or a bulk addition method.
また処理剤の性質によっては水又はアルコール溶剤など
で希釈して用いてもよい。Further, depending on the properties of the processing agent, it may be used after being diluted with water or an alcohol solvent.
また、水酸化マグネシウムの生産ライン工程での処理も
できる。これは生産ライン工程で水酸化マグネシウムは
スラリー状で上がり、このとき表面処理剤を一括投入し
充分に攪拌処理を行ない、乾燥工程を行なうことももち
ろんできる。It can also be processed in the magnesium hydroxide production line process. This is done in the production line process, where the magnesium hydroxide is produced in the form of a slurry, and at this time, the surface treatment agent can be added all at once, sufficiently stirred, and the drying process can of course be carried out.
(5)混合、混練方法
これらの各成分はそれぞれ計量混合され、従来のゴムプ
ラスチックのための装置と方法が利用でき特別の装置を
必要としない。すなわちリボンブレンダー、ヘンシェル
ミキサー等の混合攪拌機を用いて各成分を充分混合分散
させたのち、パンバリロール、押出機等の溶融混線機で
混練し目的物を得る。(5) Mixing and kneading method These components are individually measured and mixed, and conventional equipment and methods for rubber plastics can be used, and no special equipment is required. That is, each component is sufficiently mixed and dispersed using a mixer such as a ribbon blender or a Henschel mixer, and then kneaded using a melt mixer such as a panburi roll or an extruder to obtain the desired product.
(6)成形
成形は、主に射出成形、押出成形等により、(5)で得
たペレットを具体的な形状、主にボックス型の収納ケー
スやジヨイントや、テープ状、チューブ状など任意の形
状の金型およびダイスを用いて成形できる。(6) Molding is performed mainly by injection molding, extrusion molding, etc., to form the pellets obtained in (5) into specific shapes, mainly box-shaped storage cases, joints, tape shapes, tube shapes, etc. Can be molded using molds and dies.
本発明はポリスチレン、ABS、ナイロン等の有害ガス
を発生する樹脂を使用せず、密度が0.92以下の低結
晶性の、α−オレフィンの重合体およびα−オレフィン
の共重合体を使用することによって、更には1種以上の
シランカップリング剤、シリコーン誘導体又は脂肪酸、
脂肪酸金属塩で表面処理した水酸化マグネシウムを使用
することによって、多量の水酸化マグネシウムを高充填
でき、燃焼向上の為にカーボンブラック等の炭素粉末を
使用することなしに、用途によって目的に応じた難燃性
およびカラーリングが可能であり、しかも非常に柔軟で
、低温特性および加工性に優れた難燃組成物を提供でき
るものである。The present invention does not use resins that generate harmful gases such as polystyrene, ABS, and nylon, but uses low-crystalline α-olefin polymers and α-olefin copolymers with a density of 0.92 or less. Possibly also one or more silane coupling agents, silicone derivatives or fatty acids,
By using magnesium hydroxide whose surface has been treated with fatty acid metal salts, it is possible to charge a large amount of magnesium hydroxide, and it can be used in various ways depending on the purpose, without using carbon powder such as carbon black to improve combustion. It is possible to provide a flame-retardant composition that is flame-retardant and can be colored, is extremely flexible, and has excellent low-temperature properties and processability.
以下実施例をあげて説明する。 This will be explained below by giving examples.
実施例1〜7の各難燃性混和物を下記表1に従って各々
配合し、パンバリロールで溶融混練し目的物を得た。ま
た水酸化マグネシウムの表面処理は処理剤を加えてスー
パーミキサーで高速30分処理を行なった。次にチュー
ブ押出加工性、脆化温度、有害ガス成分、伸び、加熱変
形率、燃焼性の各特性を調べた。Each of the flame-retardant mixtures of Examples 1 to 7 was blended according to Table 1 below, and melt-kneaded using a panburi roll to obtain the desired product. In addition, the surface treatment of magnesium hydroxide was carried out by adding a treating agent and performing high-speed treatment for 30 minutes in a super mixer. Next, the tube extrusion processability, embrittlement temperature, harmful gas components, elongation, thermal deformation rate, and combustibility were investigated.
これらの結果を表1に示す。These results are shown in Table 1.
Claims (2)
体又はα−オレフィンの共重合体樹脂100重量部に対
して、(1) For 100 parts by weight of an α-olefin homopolymer or α-olefin copolymer resin having a density of 0.92 or less,
導体又は脂肪酸、脂肪酸金属塩で表面処理した水酸化マ
グネシウム50〜250重量部を添加してなるオレフィ
ン系難燃樹脂組成物。(2) An olefin flame-retardant resin composition containing 50 to 250 parts by weight of magnesium hydroxide surface-treated with one or more silane coupling agents, silicone derivatives, fatty acids, or fatty acid metal salts.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP797486A JPS62167339A (en) | 1986-01-20 | 1986-01-20 | Flame-retardant resin composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP797486A JPS62167339A (en) | 1986-01-20 | 1986-01-20 | Flame-retardant resin composition |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS62167339A true JPS62167339A (en) | 1987-07-23 |
Family
ID=11680430
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP797486A Pending JPS62167339A (en) | 1986-01-20 | 1986-01-20 | Flame-retardant resin composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62167339A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62212446A (en) * | 1986-03-13 | 1987-09-18 | Mitsui Petrochem Ind Ltd | Vulcanizable rubber composition |
JPH0238434A (en) * | 1988-07-29 | 1990-02-07 | Nippon Unicar Co Ltd | Flame-retarding polyolefin resin composition |
WO1998046673A1 (en) | 1997-04-17 | 1998-10-22 | Duslo, A.S. S^¿Ala | A polymeric composite material with improved flame resistance |
WO2005103138A1 (en) * | 2004-04-20 | 2005-11-03 | Yazaki Corporation | Polyolefin resin composition and electric wires made by using the same |
US7799857B2 (en) | 2005-05-20 | 2010-09-21 | Sun Allomer Ltd. | Flame-retardant thermoplastic resin composition, molded product thereof and electric wire |
US8313674B2 (en) | 2004-08-11 | 2012-11-20 | Sun Allomer Ltd. | Flame-retardant polyolefin resin composition |
-
1986
- 1986-01-20 JP JP797486A patent/JPS62167339A/en active Pending
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62212446A (en) * | 1986-03-13 | 1987-09-18 | Mitsui Petrochem Ind Ltd | Vulcanizable rubber composition |
JPH0238434A (en) * | 1988-07-29 | 1990-02-07 | Nippon Unicar Co Ltd | Flame-retarding polyolefin resin composition |
WO1998046673A1 (en) | 1997-04-17 | 1998-10-22 | Duslo, A.S. S^¿Ala | A polymeric composite material with improved flame resistance |
WO2005103138A1 (en) * | 2004-04-20 | 2005-11-03 | Yazaki Corporation | Polyolefin resin composition and electric wires made by using the same |
US8313674B2 (en) | 2004-08-11 | 2012-11-20 | Sun Allomer Ltd. | Flame-retardant polyolefin resin composition |
US7799857B2 (en) | 2005-05-20 | 2010-09-21 | Sun Allomer Ltd. | Flame-retardant thermoplastic resin composition, molded product thereof and electric wire |
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