JPH0593108A - Flame-retardant resin composition - Google Patents
Flame-retardant resin compositionInfo
- Publication number
- JPH0593108A JPH0593108A JP3253984A JP25398491A JPH0593108A JP H0593108 A JPH0593108 A JP H0593108A JP 3253984 A JP3253984 A JP 3253984A JP 25398491 A JP25398491 A JP 25398491A JP H0593108 A JPH0593108 A JP H0593108A
- Authority
- JP
- Japan
- Prior art keywords
- ethylene
- resin
- copolymer
- pts
- flame
- 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
- 239000003063 flame retardant Substances 0.000 title claims abstract description 9
- 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 abstract description 8
- 239000011342 resin composition Substances 0.000 title claims description 6
- 229920005989 resin Polymers 0.000 claims abstract description 20
- 239000011347 resin Substances 0.000 claims abstract description 20
- 229920001577 copolymer Polymers 0.000 claims abstract description 11
- 239000004925 Acrylic resin Substances 0.000 claims abstract description 6
- 229920000178 Acrylic resin Polymers 0.000 claims abstract description 6
- 239000004711 α-olefin Substances 0.000 claims abstract description 6
- 229920003229 poly(methyl methacrylate) Polymers 0.000 claims abstract description 5
- 239000004926 polymethyl methacrylate Substances 0.000 claims abstract description 5
- 150000002736 metal compounds Chemical class 0.000 claims description 11
- 239000000203 mixture Substances 0.000 claims description 10
- 229920006122 polyamide resin Polymers 0.000 claims description 8
- 229920006026 co-polymeric resin Polymers 0.000 claims description 7
- 229920006244 ethylene-ethyl acrylate Polymers 0.000 claims description 6
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 5
- 229920005680 ethylene-methyl methacrylate copolymer Polymers 0.000 claims description 4
- 150000004756 silanes Chemical class 0.000 claims description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 3
- 239000005977 Ethylene Substances 0.000 claims description 3
- HBGPNLPABVUVKZ-POTXQNELSA-N (1r,3as,4s,5ar,5br,7r,7ar,11ar,11br,13as,13br)-4,7-dihydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1h-cyclopenta[a]chrysen-9-one Chemical compound C([C@@]12C)CC(=O)C(C)(C)[C@@H]1[C@H](O)C[C@]([C@]1(C)C[C@@H]3O)(C)[C@@H]2CC[C@H]1[C@@H]1[C@]3(C)CC[C@H]1C(=C)C HBGPNLPABVUVKZ-POTXQNELSA-N 0.000 claims description 2
- PFRGGOIBYLYVKM-UHFFFAOYSA-N 15alpha-hydroxylup-20(29)-en-3-one Natural products CC(=C)C1CCC2(C)CC(O)C3(C)C(CCC4C5(C)CCC(=O)C(C)(C)C5CCC34C)C12 PFRGGOIBYLYVKM-UHFFFAOYSA-N 0.000 claims description 2
- SOKRNBGSNZXYIO-UHFFFAOYSA-N Resinone Natural products CC(=C)C1CCC2(C)C(O)CC3(C)C(CCC4C5(C)CCC(=O)C(C)(C)C5CCC34C)C12 SOKRNBGSNZXYIO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 abstract description 7
- 150000002367 halogens Chemical class 0.000 abstract description 7
- 229910052751 metal Inorganic materials 0.000 abstract description 6
- 239000002184 metal Substances 0.000 abstract description 6
- 238000005299 abrasion Methods 0.000 abstract description 3
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 abstract description 3
- 229910000077 silane Inorganic materials 0.000 abstract description 3
- 229920000089 Cyclic olefin copolymer Polymers 0.000 abstract description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 abstract description 2
- 238000013329 compounding Methods 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 229920002647 polyamide Polymers 0.000 abstract 1
- 230000000694 effects Effects 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 3
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- DCTOHCCUXLBQMS-UHFFFAOYSA-N 1-undecene Chemical compound CCCCCCCCCC=C DCTOHCCUXLBQMS-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- 239000004677 Nylon Substances 0.000 description 2
- 229920002292 Nylon 6 Polymers 0.000 description 2
- 229920002302 Nylon 6,6 Polymers 0.000 description 2
- -1 acrylic ester Chemical class 0.000 description 2
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 239000000347 magnesium hydroxide Substances 0.000 description 2
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 239000000779 smoke Substances 0.000 description 2
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 1
- CRSBERNSMYQZNG-UHFFFAOYSA-N 1-dodecene Chemical compound CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 description 1
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-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
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-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
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 229920000571 Nylon 11 Polymers 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- 229920001007 Nylon 4 Polymers 0.000 description 1
- 229920000305 Nylon 6,10 Polymers 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- VCNTUJWBXWAWEJ-UHFFFAOYSA-J aluminum;sodium;dicarbonate Chemical compound [Na+].[Al+3].[O-]C([O-])=O.[O-]C([O-])=O VCNTUJWBXWAWEJ-UHFFFAOYSA-J 0.000 description 1
- 239000003429 antifungal agent Substances 0.000 description 1
- 229940121375 antifungal agent Drugs 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- RQPZNWPYLFFXCP-UHFFFAOYSA-L barium dihydroxide Chemical compound [OH-].[OH-].[Ba+2] RQPZNWPYLFFXCP-UHFFFAOYSA-L 0.000 description 1
- 229910001863 barium hydroxide Inorganic materials 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 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
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000000805 composite resin Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 229910001647 dawsonite Inorganic materials 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- GDVKFRBCXAPAQJ-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Al+3].[Al+3].[O-]C([O-])=O GDVKFRBCXAPAQJ-UHFFFAOYSA-A 0.000 description 1
- 150000001990 dicarboxylic acid derivatives Chemical class 0.000 description 1
- ZIWYFFIJXBGVMZ-UHFFFAOYSA-N dioxotin hydrate Chemical compound O.O=[Sn]=O ZIWYFFIJXBGVMZ-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- CWAFVXWRGIEBPL-UHFFFAOYSA-N ethoxysilane Chemical compound CCO[SiH3] CWAFVXWRGIEBPL-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 150000002366 halogen compounds Chemical class 0.000 description 1
- 229910001701 hydrotalcite Inorganic materials 0.000 description 1
- 229960001545 hydrotalcite Drugs 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 239000012796 inorganic flame retardant Substances 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- 239000000314 lubricant Substances 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
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- GGROONUBGIWGGS-UHFFFAOYSA-N oxygen(2-);zirconium(4+);hydrate Chemical compound O.[O-2].[O-2].[Zr+4] GGROONUBGIWGGS-UHFFFAOYSA-N 0.000 description 1
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 150000003003 phosphines Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 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
- 150000003839 salts Chemical class 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- SGCFZHOZKKQIBU-UHFFFAOYSA-N tributoxy(ethenyl)silane Chemical compound CCCCO[Si](OCCCC)(OCCCC)C=C SGCFZHOZKKQIBU-UHFFFAOYSA-N 0.000 description 1
- UMFJXASDGBJDEB-UHFFFAOYSA-N triethoxy(prop-2-enyl)silane Chemical compound CCO[Si](CC=C)(OCC)OCC UMFJXASDGBJDEB-UHFFFAOYSA-N 0.000 description 1
- LFRDHGNFBLIJIY-UHFFFAOYSA-N trimethoxy(prop-2-enyl)silane Chemical compound CO[Si](OC)(OC)CC=C LFRDHGNFBLIJIY-UHFFFAOYSA-N 0.000 description 1
- BIKXLKXABVUSMH-UHFFFAOYSA-N trizinc;diborate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]B([O-])[O-].[O-]B([O-])[O-] BIKXLKXABVUSMH-UHFFFAOYSA-N 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Organic Insulating Materials (AREA)
- Insulated Conductors (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、火災発生による燃焼に
よっても有害かつ腐蝕性のハロゲン系ガスを全く発生し
ない、電線、ケーブル等の被覆、ホース類、シートおよ
び射出製品等への適用を目的とした難燃性樹脂組成物に
関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention is intended to be applied to coatings of electric wires and cables, hoses, sheets, injection products, etc., which do not generate harmful and corrosive halogen-based gas even when burned by a fire. And a flame-retardant resin composition.
【0002】[0002]
【従来の技術】従来、電線、ケーブル等の被覆、ホース
類、シートおよび射出製品等に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
ハロゲン組成物であり、燃焼時にハロゲン系ガスを発生
するので人体に有害であり、かつ金属が腐蝕されるため
好ましくなかった。また発煙量が多く、視界が悪いた
め、火災時の人の避難および消火活動が著しく制限され
ていた。2. Description of the Related Art Conventionally, in order to impart flame retardancy to a polyolefin composition which has been widely used for coating electric wires and cables, hoses, sheets and injection products, a halogen compound and antimony trioxide are added to the polyolefin. It was achieved by adding. However, these compositions are halogen compositions, which are not preferable because they generate a halogen-based gas when burned, which is harmful to the human body and corrodes metals. Also, due to the large amount of smoke emitted and poor visibility, evacuation and extinguishing activities of people during a fire were significantly limited.
【0003】特に、最近は安全面からこのようなハロゲ
ン系ガスを発生しないことが強く要望されるようになっ
てきた。このような情勢を踏まえ、発煙性、有害性の非
常に少ない水和金属化合物を用いる無機系難燃剤が注目
されるようになってきた。近年、難燃性を付与するため
に、水酸化マグネシウム、水酸化アルミニウム等を含む
樹脂複合物が実用化されているが、実際に、難燃性を得
るためにはこれらの水和金属化合物を多量に充填する必
要があり、そのため、表面が傷つき易く、摩擦によって
表面が摩耗し易いという問題があった。In particular, recently, from the viewpoint of safety, it has been strongly demanded that such a halogen-based gas should not be generated. In view of such circumstances, attention has been paid to inorganic flame retardants that use hydrated metal compounds that emit extremely little smoke and are less harmful. In recent years, resin composites containing magnesium hydroxide, aluminum hydroxide and the like have been put to practical use in order to impart flame retardancy, but actually, in order to obtain flame retardancy, these hydrated metal compounds are used. Since it is necessary to fill a large amount, there is a problem that the surface is easily scratched and the surface is easily worn by friction.
【0004】このような問題を解決するため、これまで
に樹脂と無機物との相溶性を向上させるため、オレフィ
ン系シラングラフトマーを添加する方法、ジカルボン酸
誘導体または無水ジカルボン酸誘導体を添加する方法、
或は、組成物に表面活性を付与するためにシリコーン組
成物を添加する方法、ワックス、界面活性剤を表面にブ
リードさせる方法等が提案されているが、特に表面の傷
つきにくさ、耐摩耗性が要求される分野では不十分であ
った。In order to solve the above problems and to improve the compatibility between the resin and the inorganic substance, a method of adding an olefinic silane graftmer, a method of adding a dicarboxylic acid derivative or a dicarboxylic acid anhydride derivative,
Alternatively, a method of adding a silicone composition in order to impart surface activity to the composition, a method of bleeding a wax or a surfactant on the surface, and the like have been proposed. Was not enough in the required field.
【0005】[0005]
【発明が解決しようとする課題】本発明は、燃焼時に有
害なハロゲン系ガスを発生せず、水和金属化合物を添加
することによって得られた高度の難燃性を失うことな
く、かつ柔軟性を保持し、耐摩耗性が大幅に改善された
難燃性樹脂組成物の提供を目的としたものである。DISCLOSURE OF THE INVENTION The present invention does not generate harmful halogen-based gas upon combustion, does not lose the high flame retardancy obtained by adding a hydrated metal compound, and is flexible. The purpose of the present invention is to provide a flame-retardant resin composition that retains the above and has significantly improved abrasion resistance.
【0006】[0006]
【課題を解決するための手段】本発明の難燃性樹脂組成
物は下記の(a)〜(d)の成分からなる組成物であって、
(a)+(b)100重量部(但し(a):(b)=97:3〜5
0:50)に対して、(c)を0.1〜30重量部および(d)
を50〜300重量部含有することを特徴とするもので
ある。 (a)エチレンとα−オレフィンとの共重合体、エチレン
−エチルアクリレート共重合樹脂またはエチレン−メチ
ルメタクリレート共重合樹脂の中から選ばれる1種また
は2種以上の樹脂、(b)ポリアミド樹脂、(c)エチレン
−グリシジルメチルアクリレート共重合樹脂、エチレン
−エチルアクリレート−無水マレイン酸共重合樹脂、エ
チレン−アクリル酸エステル共重合樹脂のシラン誘導
体、ポリメチルメタクリレート又はアクリル系樹脂のカ
ルボン酸誘導体の中から選ばれる1種または2種以上の
樹脂、及び(d)水和金属化合物。The flame-retardant resin composition of the present invention is a composition comprising the following components (a) to (d):
(a) + (b) 100 parts by weight (however, (a) :( b) = 97: 3-5)
0:50), 0.1 to 30 parts by weight of (c) and (d)
Is contained in an amount of 50 to 300 parts by weight. (a) one or more resins selected from a copolymer of ethylene and α-olefin, an ethylene-ethyl acrylate copolymer resin or an ethylene-methyl methacrylate copolymer resin, (b) a polyamide resin, ( c) selected from ethylene-glycidyl methyl acrylate copolymer resin, ethylene-ethyl acrylate-maleic anhydride copolymer resin, silane derivative of ethylene-acrylic ester copolymer resin, polymethyl methacrylate or carboxylic acid derivative of acrylic resin One or more kinds of resins described above, and (d) a hydrated metal compound.
【0007】本発明の(a)成分は、水和金属化合物を多
量に充填した場合に引き起こされる、特性の低下を防止
する目的で添加される。本発明において使用されるエチ
レンとα−オレフィンとの共重合体のα−オレフィンと
しては、C3 〜C12の例えばプロピレン、ブテン−1、
ペンテン−1、ヘキセン−1、ヘプテン−1、オクテン
−1、4−メチルペンテン−1、4−メチルヘキセン−
1、4,4−ジメチルペンテン−1、ノネン−1、デセ
ン−1、ウンデセン−1およびドデセン−1等が挙げ
ら、これらの樹脂とエチレン−エチルアクリレート共重
合樹脂またはエチレン−メチルメタクリレート共重合樹
脂の中から選ばれる1種または2種以上の樹脂が使用さ
れる。The component (a) of the present invention is added for the purpose of preventing the deterioration of properties caused when a large amount of a hydrated metal compound is filled. Examples of the α-olefin of the copolymer of ethylene and α-olefin used in the present invention include C 3 to C 12 such as propylene, butene-1,
Pentene-1, hexene-1, heptene-1, octene-1, 4-methylpentene-1, 4-methylhexene-
1,4,4-dimethylpentene-1, nonene-1, decene-1, undecene-1, and dodecene-1, etc., and these resins and ethylene-ethyl acrylate copolymer resin or ethylene-methyl methacrylate copolymer resin. One or more resins selected from the above are used.
【0008】本発明の(b)成分は組成物の耐摩耗性を改
良する目的で添加される。本発明において使用されるポ
リアミド樹脂としては、ナイロン−4、ナイロン−6、
ナイロン−11、ナイロン−12、ナイロン−6,6、
ナイロン−6,10、ナイロン6,12、ナイロン1
1,6およびナイロン−6とナイロン−6,6との共重
合体等が挙げられる。これらの添加量としては、(a)成
分との割合で3重量%以下では所望の耐摩耗性向上の効
果が得にくく、また50重量%以上では柔軟性、難燃性
の低下を招き、製品も高価になるため実用的でない。The component (b) of the present invention is added for the purpose of improving the wear resistance of the composition. The polyamide resin used in the present invention includes nylon-4, nylon-6,
Nylon-11, Nylon-12, Nylon-6,6,
Nylon-6,10, Nylon 6,12, Nylon 1
1,6 and a copolymer of nylon-6 and nylon-6,6 and the like. If the amount of these components added is 3% by weight or less with respect to the component (a), it is difficult to obtain the desired effect of improving wear resistance, and if it is 50% by weight or more, flexibility and flame retardancy are deteriorated. Is not practical because it becomes expensive.
【0009】本発明において使用される(c)成分はポリ
アミド樹脂と(a)成分で示される樹脂との相溶性および
水和金属化合物との相溶性を向上させるために添加する
ものである。本発明において使用されるエチレン−アク
リル酸エステル共重合樹脂のシラン誘導体のアクリル酸
エステルとしては、エチルアクリレート、メチルアクリ
レート、メチルメタクリレート等が挙げられ、またシラ
ン化合物としては、ビニルトリメトキシシラン、ビニル
トリエトキシシラン、ビニルトリブトキシシラン、アリ
ルトリメトキシシラン、アリルトリエトキシシラン等が
挙げられる。またアクリル系樹脂のカルボン酸誘導体の
アクリル系樹脂としては、ポリメチルメタクリレート、
エチレン−メチルメタクリレート共重合体、エチレン−
メチルアクリレート共重合体、エチレン−エチルアクリ
レート共重合体等が挙げられ、またカルボン酸として
は、アクリル酸、メタクリル酸、フマル酸、無水マレイ
ン酸、イタコン酸等が挙げられる。これらの添加量とし
ては、(a)成分+(b)成分100重量部に対して 0.1
重量部以下ではポリアミド樹脂と他の添加剤との相溶性
が劣るため機械的特性、特に伸びが劣る。また30重量
部以上では、本発明の示す改善効果を上回る著しい効果
を示さず、製品も高価になるため実用的でない。The component (c) used in the present invention is added to improve the compatibility between the polyamide resin and the resin represented by the component (a) and the compatibility with the hydrated metal compound. Examples of the acrylic ester of the silane derivative of the ethylene-acrylic ester copolymer resin used in the present invention include ethyl acrylate, methyl acrylate, methyl methacrylate, and the like, and the silane compound includes vinyltrimethoxysilane and vinyltrimethoxysilane. Examples thereof include ethoxysilane, vinyltributoxysilane, allyltrimethoxysilane, and allyltriethoxysilane. Further, as the acrylic resin of the carboxylic acid derivative of the acrylic resin, polymethylmethacrylate,
Ethylene-methyl methacrylate copolymer, ethylene-
Examples thereof include methyl acrylate copolymers and ethylene-ethyl acrylate copolymers, and examples of carboxylic acids include acrylic acid, methacrylic acid, fumaric acid, maleic anhydride, and itaconic acid. The amount of these added is 0.1 with respect to 100 parts by weight of the component (a) + the component (b).
If it is less than 1 part by weight, the compatibility between the polyamide resin and the other additives is poor, so that the mechanical properties, especially the elongation are poor. On the other hand, when the amount is 30 parts by weight or more, no remarkable effect exceeding the improving effect of the present invention is exhibited and the product becomes expensive, which is not practical.
【0010】本発明において使用される水和金属化合物
としては、分解開始温度が150〜450℃の範囲にあって、
一般式 MmOn・XH2O(ここに Mは金属、m,nは金属の原子
価によって定まる1以上の整数、Xは含有結晶水を示す
数)で表される化合物または該化合物を含む複塩であ
り、具体的には、水酸化アルミニウム(Al2O3・3H2O;
または Al(OH)3)、水酸化マグネシウム(MgO・H2O;ま
たは Mg(OH)2)、水酸化カルシウム(CaO・H2O;または
Ca(OH)2)、水酸化バリウム(BaO・H2O;またはBaO・9
H2O)、酸化ジルコニウム水和物(ZrO・nH20)、酸化ス
ズ水和物(SnO・H20)、塩基性炭酸マグネシウム(3MgC
O3・Mg(OH)2・3H2O)、ハイドロタルサイト(6MgO・Al2
O3・H2O)、ドウソナイト(Na2CO3・Al2O3・nH2O)、硼
砂(Na2O・B2O5・5H2O)、ホウ酸亜鉛(ZnB4O7・2ZnO)
等である。これらの添加量としては、(a)成分+(b)成
分100重量部に対して、50重量部以下では所望の難
燃効果は得にくく、また300重量部以上では抗張力な
どの機械的物性が低下し、また押出加工性が悪くなる。The hydrated metal compound used in the present invention has a decomposition initiation temperature in the range of 150 to 450 ° C.,
A compound represented by the general formula M m O n · XH 2 O (where M is a metal, m and n are integers of 1 or more determined by the valence of the metal, and X is a number of contained waters of crystallization), or a compound represented by the formula It is a double salt containing, specifically, aluminum hydroxide (Al 2 O 3 .3H 2 O;
Or Al (OH) 3 ), magnesium hydroxide (MgO · H 2 O; or Mg (OH) 2 ), calcium hydroxide (CaO · H 2 O; or
Ca (OH) 2 ), barium hydroxide (BaO ・ H 2 O; or BaO ・ 9
H 2 O), zirconium oxide hydrate (ZrO ・ nH 2 0), tin oxide hydrate (SnO ・ H 2 0), basic magnesium carbonate (3MgC
O 3 · Mg (OH) 2 · 3H 2 O), hydrotalcite (6MgO · Al 2
O 3 · H 2 O), dawsonite (Na 2 CO 3 · Al 2 O 3 · nH 2 O), borax (Na 2 O · B 2 O 5 · 5H 2 O), zinc borate (ZnB 4 O 7 · 2ZnO)
Etc. As for the amount of addition of these components, if the amount is 50 parts by weight or less relative to 100 parts by weight of the component (a) + the component (b), it is difficult to obtain the desired flame retardant effect. And the extrusion processability deteriorates.
【0011】その他の添加剤として本発明の難燃性組成
物は所望により通常に使用される添加剤、例えば酸化防
止剤、中和剤、紫外線吸収剤、帯電防止剤、顔料、分散
剤、滑材、増粘剤、発泡剤、金属劣化防止剤、防カビ
剤、流動調整剤等、またリン及びホスフィン誘導体の難
燃剤、その他の無機質充填剤、架橋剤、架橋助剤等、ま
たは他の合成樹脂を含有させることもできる。また電子
線照射架橋させることも可能である。As other additives, the flame-retardant composition of the present invention may optionally contain additives usually used, for example, antioxidants, neutralizing agents, ultraviolet absorbers, antistatic agents, pigments, dispersants, lubricants. Materials, thickeners, foaming agents, metal deterioration inhibitors, antifungal agents, flow regulators, etc., flame retardants of phosphorus and phosphine derivatives, other inorganic fillers, crosslinking agents, crosslinking aids, etc., or other synthetic materials A resin can also be included. It is also possible to carry out electron beam irradiation for crosslinking.
【0012】[0012]
【実施例】以下に実施例を挙げて説明する。表1に示す
ような配合割合に従って各成分を異方向2軸押出機を用
いて押出温度200〜240℃で混練し、造粒した。得られた
組成物をロールプレスし、各種測定用試験片を作成し
た。この試験片を用いて引張破断伸び、酸素指数、摩耗
試験を実施した。また押出機によって外径20mmφ、内径
18mmφ、厚さ1mmのチューブの押出を行い、押出加工性
の評価を行った。EXAMPLES Examples will be described below. Each component was kneaded at an extrusion temperature of 200 to 240 ° C. by using a different-direction twin-screw extruder according to the blending ratio as shown in Table 1, and granulated. The obtained composition was roll-pressed to prepare various measurement test pieces. Using this test piece, tensile breaking elongation, oxygen index and wear test were carried out. Also, depending on the extruder, the outer diameter is 20 mmφ and the inner diameter is
A tube having a diameter of 18 mm and a thickness of 1 mm was extruded to evaluate the extrudability.
【0013】[0013]
【表1】 [Table 1]
【0014】(1)日本石油化学製 ソフトレックス(エチ
レン−α−オレフィン共重合体) (2)日本石油化学製 レクスロン (エチレン−エチルア
クリレート共重合体) (3)住友化学工業製 低密度ポリエチレン (4)住友化学工業製 エチレン−グリシジルメチルアクリ
レート共重合体 (5)住友化学工業製 エチレン−エチルアクリレート−無
水マレイン酸共重合体 (6)ROHM & HAAS社製 アクリル系樹脂のカルボン酸誘導
体 (7)呉羽化学工業製 ポリメチルメタクリレート (8)三井デュポンポリケミカル製 エチレン−エチルアク
リレート共重合樹脂のシラン誘導体 (9)昭和電工製 ハイジライト H42M (10)協和化学製 キスマ 5B (11)三洋化成工業製 サンワックス 171P 1.0重量部 チバガイギー製 イルガノックス 1076 0.3重量部 及
び 住友化学工業製 スミライザー WXR 0.3重量部の混
合物 (12)顔料 黒の場合:VALCAN 9A-32 3.0重量部 (13)JIS K6760 による。 (14)JIS K7201 による。 (15)摩耗輪 CS-10、荷重 500g、1000回転。 (16)50mmφの単軸押出機 160-165-170-180℃L/D:25
圧縮比 3.5 チューブ押出外径 20mmφ、内径 18mmφ 評価 優>良>可>不可の順とし、可のレベルまでを合
格とした。(1) Nippon Petrochemical Softlex (ethylene-α-olefin copolymer) (2) Nippon Petrochemical Lexulon (ethylene-ethyl acrylate copolymer) (3) Sumitomo Chemical low density polyethylene ( 4) Sumitomo Chemical Co., Ltd. ethylene-glycidyl methyl acrylate copolymer (5) Sumitomo Chemical Co., Ltd. ethylene-ethyl acrylate-maleic anhydride copolymer (6) ROHM & HAAS acrylic resin carboxylic acid derivative (7) Kureha Chemical Industry Polymethyl Methacrylate (8) Mitsui DuPont Polychemical Silane Derivative of Ethylene-Ethyl Acrylate Copolymer Resin (9) Showa Denko Heidilite H42M (10) Kyowa Chemical Kisuma 5B (11) Sanyo Chemical Industries Sun Wax 171P 1.0 parts by weight Ciba Geigy Irganox 1076 0.3 parts by weight and Sumitomo Chemical Sumilizer WXR 0.3 parts by weight Material (12) Pigment Black: VALCAN 9A-32 3.0 parts by weight (13) According to JIS K6760. (14) According to JIS K7201. (15) Worn wheel CS-10, load 500g, 1000 rotations. (16) 50mmφ single screw extruder 160-165-170-180 ℃ L / D: 25
Compression ratio 3.5 Tube extrusion Outer diameter 20 mmφ, Inner diameter 18 mmφ Evaluation Excellent>Good>Acceptable> Impossible, in order of acceptable level.
【0015】表1から明らかなように、実施例1〜4に
示す材料は難燃性を維持し、ポリアミド樹脂の添加によ
り良好な耐摩耗性を示し、かつポリマーと水和金属化合
物との相溶性が極めて良好で、非常に優れた加工性およ
び破断時伸び値を示している。これに対し比較例1で
は、ポリアミド樹脂を添加していないため耐摩耗性が劣
り、ポリアミド樹脂添加量の多い比較例2では柔軟性が
劣り、破断時伸び値も大幅に低下している。相溶化剤と
しての(c)成分を添加していない比較例3では破断時伸
び値が大幅に低下している。また水和金属化合物の添加
量が少ない比較例4では難燃性が劣り、水和金属化合物
の添加量が300重量部を越える比較例5は加工性が悪
い。As is clear from Table 1, the materials shown in Examples 1 to 4 maintain flame retardancy, exhibit good wear resistance by the addition of the polyamide resin, and form the phase of the polymer and the hydrated metal compound. It has very good solubility and shows very good workability and elongation at break. On the other hand, in Comparative Example 1, since no polyamide resin was added, wear resistance was poor, and in Comparative Example 2 in which the amount of polyamide resin added was large, the flexibility was poor and the elongation at break value was also significantly reduced. In Comparative Example 3 in which the component (c) as the compatibilizer was not added, the elongation at break value was significantly reduced. Further, in Comparative Example 4 in which the addition amount of the hydrated metal compound is small, the flame retardancy is poor, and in Comparative Example 5 in which the addition amount of the hydrated metal compound exceeds 300 parts by weight, the workability is poor.
【0016】[0016]
【発明の効果】以上説明したように、本発明によれば、
燃焼時に有害なハロゲン系ガスを発生せず、高度の難燃
性と柔軟性を保持するとともに、耐摩耗性の大幅に向上
した樹脂組成物を得ることができる。As described above, according to the present invention,
It is possible to obtain a resin composition which does not generate a harmful halogen-based gas at the time of combustion, retains a high degree of flame retardancy and flexibility, and has significantly improved abrasion resistance.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 H01B 3/44 P 9059−5G // H01B 7/34 B 7244−5G ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification code Internal reference number FI Technical indication H01B 3/44 P 9059-5G // H01B 7/34 B 7244-5G
Claims (1)
であって、(a)+(b)100重量部(但し(a):(b)=
97:3〜50:50)に対して、(c)を0.1〜30重量部お
よび(d)を50〜300重量部含有することを特徴とす
る難燃性樹脂組成物。 (a)エチレンとα−オレフィンとの共重合体、エチレン
−エチルアクリレート共重合樹脂またはエチレン−メチ
ルメタクリレート共重合樹脂の中から選ばれる1種また
は2種以上の樹脂、 (b)ポリアミド樹脂、 (c)エチレン−グリシジルメチルアクリレート共重合樹
脂、エチレン−エチルアクリレート−無水マレイン酸共
重合樹脂、エチレン−アクリル酸エステル共重合樹脂の
シラン誘導体、ポリメチルメタクリレート又はアクリル
系樹脂のカルボン酸誘導体の中から選ばれる1種または
2種以上の樹脂、及び (d)水和金属化合物。1. A composition comprising the following components (a) to (d), wherein (a) + (b) 100 parts by weight (where (a) :( b) =
97: 3 to 50:50), 0.1 to 30 parts by weight of (c) and 50 to 300 parts by weight of (d) are contained in the flame-retardant resin composition. (a) one or more resins selected from a copolymer of ethylene and α-olefin, an ethylene-ethyl acrylate copolymer resin or an ethylene-methyl methacrylate copolymer resin, (b) a polyamide resin, c) selected from ethylene-glycidyl methyl acrylate copolymer resin, ethylene-ethyl acrylate-maleic anhydride copolymer resin, silane derivative of ethylene-acrylic ester copolymer resin, polymethyl methacrylate or carboxylic acid derivative of acrylic resin One or more kinds of resins, and (d) a hydrated metal compound.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3253984A JPH0593108A (en) | 1991-10-02 | 1991-10-02 | Flame-retardant resin composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3253984A JPH0593108A (en) | 1991-10-02 | 1991-10-02 | Flame-retardant resin composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0593108A true JPH0593108A (en) | 1993-04-16 |
Family
ID=17258657
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3253984A Pending JPH0593108A (en) | 1991-10-02 | 1991-10-02 | Flame-retardant resin composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0593108A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0704489A1 (en) | 1994-09-28 | 1996-04-03 | Elf Atochem S.A. | Flame resistant polyamide compositions and their use as coating of electrical cables |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04277540A (en) * | 1991-03-05 | 1992-10-02 | Idemitsu N S G Kk | Flame-retardant resin composition |
-
1991
- 1991-10-02 JP JP3253984A patent/JPH0593108A/en active Pending
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04277540A (en) * | 1991-03-05 | 1992-10-02 | Idemitsu N S G Kk | Flame-retardant resin composition |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0704489A1 (en) | 1994-09-28 | 1996-04-03 | Elf Atochem S.A. | Flame resistant polyamide compositions and their use as coating of electrical cables |
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