RU2207352C2 - Способ замедления горения полимерного субстрата и композиция ингибитора горения - Google Patents
Способ замедления горения полимерного субстрата и композиция ингибитора горения Download PDFInfo
- Publication number
- RU2207352C2 RU2207352C2 RU2000102671/04A RU2000102671A RU2207352C2 RU 2207352 C2 RU2207352 C2 RU 2207352C2 RU 2000102671/04 A RU2000102671/04 A RU 2000102671/04A RU 2000102671 A RU2000102671 A RU 2000102671A RU 2207352 C2 RU2207352 C2 RU 2207352C2
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- Russia
- Prior art keywords
- alkyl
- carbon atoms
- group
- hydrogen
- substituted
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- 229920000307 polymer substrate Polymers 0.000 title claims abstract 10
- 239000003112 inhibitor Substances 0.000 title claims abstract 6
- 238000000034 method Methods 0.000 title claims 7
- 239000000203 mixture Substances 0.000 title claims 7
- 230000000979 retarding effect Effects 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 claims abstract 31
- -1 amino, carboxy Chemical group 0.000 claims abstract 31
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract 31
- 150000001412 amines Chemical class 0.000 claims abstract 13
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract 13
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical group CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims abstract 8
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 claims abstract 7
- 125000004817 pentamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 claims abstract 7
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims abstract 6
- 229920000642 polymer Polymers 0.000 claims abstract 5
- 150000002148 esters Chemical group 0.000 claims abstract 4
- 229920000098 polyolefin Polymers 0.000 claims abstract 4
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims abstract 4
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims abstract 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims abstract 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims abstract 2
- 229910052796 boron Inorganic materials 0.000 claims abstract 2
- 229910052698 phosphorus Inorganic materials 0.000 claims abstract 2
- 239000011574 phosphorus Substances 0.000 claims abstract 2
- 229910052710 silicon Inorganic materials 0.000 claims abstract 2
- 239000010703 silicon Substances 0.000 claims abstract 2
- 230000002195 synergetic effect Effects 0.000 claims abstract 2
- 239000001257 hydrogen Substances 0.000 claims 24
- 229910052739 hydrogen Inorganic materials 0.000 claims 24
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 22
- 125000003118 aryl group Chemical group 0.000 claims 13
- 125000002947 alkylene group Chemical group 0.000 claims 11
- 125000001931 aliphatic group Chemical group 0.000 claims 10
- KSSJBGNOJJETTC-UHFFFAOYSA-N COC1=C(C=CC=C1)N(C1=CC=2C3(C4=CC(=CC=C4C=2C=C1)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)C1=CC(=CC=C1C=1C=CC(=CC=13)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)C1=CC=C(C=C1)OC Chemical compound COC1=C(C=CC=C1)N(C1=CC=2C3(C4=CC(=CC=C4C=2C=C1)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)C1=CC(=CC=C1C=1C=CC(=CC=13)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)C1=CC=C(C=C1)OC KSSJBGNOJJETTC-UHFFFAOYSA-N 0.000 claims 8
- 239000002253 acid Substances 0.000 claims 6
- 125000003545 alkoxy group Chemical group 0.000 claims 6
- 125000003710 aryl alkyl group Chemical group 0.000 claims 6
- 150000001875 compounds Chemical class 0.000 claims 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 6
- JIHQDMXYYFUGFV-UHFFFAOYSA-N 1,3,5-triazine Chemical compound C1=NC=NC=N1 JIHQDMXYYFUGFV-UHFFFAOYSA-N 0.000 claims 5
- 238000002485 combustion reaction Methods 0.000 claims 5
- 125000000000 cycloalkoxy group Chemical group 0.000 claims 5
- 229910052757 nitrogen Inorganic materials 0.000 claims 5
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 4
- 239000005977 Ethylene Substances 0.000 claims 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims 4
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims 3
- 150000001408 amides Chemical class 0.000 claims 3
- 125000004104 aryloxy group Chemical group 0.000 claims 3
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 3
- 239000011230 binding agent Substances 0.000 claims 3
- 125000001589 carboacyl group Chemical group 0.000 claims 3
- 229920001577 copolymer Polymers 0.000 claims 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 3
- 125000001624 naphthyl group Chemical group 0.000 claims 3
- 125000003884 phenylalkyl group Chemical group 0.000 claims 3
- 125000006710 (C2-C12) alkenyl group Chemical group 0.000 claims 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- 239000007983 Tris buffer Substances 0.000 claims 2
- 125000003282 alkyl amino group Chemical group 0.000 claims 2
- 125000000732 arylene group Chemical group 0.000 claims 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 2
- OSIVCXJNIBEGCL-UHFFFAOYSA-N bis(2,2,6,6-tetramethyl-1-octoxypiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)N(OCCCCCCCC)C(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)N(OCCCCCCCC)C(C)(C)C1 OSIVCXJNIBEGCL-UHFFFAOYSA-N 0.000 claims 2
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 2
- GBXQPDCOMJJCMJ-UHFFFAOYSA-M trimethyl-[6-(trimethylazaniumyl)hexyl]azanium;bromide Chemical compound [Br-].C[N+](C)(C)CCCCCC[N+](C)(C)C GBXQPDCOMJJCMJ-UHFFFAOYSA-M 0.000 claims 2
- 125000006839 xylylene group Chemical group 0.000 claims 2
- RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidine Chemical group CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 claims 1
- 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 claims 1
- RLHGFJMGWQXPBW-UHFFFAOYSA-N 2-hydroxy-3-(1h-imidazol-5-ylmethyl)benzamide Chemical compound NC(=O)C1=CC=CC(CC=2NC=NC=2)=C1O RLHGFJMGWQXPBW-UHFFFAOYSA-N 0.000 claims 1
- RXFCIXRFAJRBSG-UHFFFAOYSA-N 3,2,3-tetramine Chemical compound NCCCNCCNCCCN RXFCIXRFAJRBSG-UHFFFAOYSA-N 0.000 claims 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims 1
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims 1
- 239000004215 Carbon black (E152) Substances 0.000 claims 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims 1
- 229910019142 PO4 Inorganic materials 0.000 claims 1
- 239000004743 Polypropylene Substances 0.000 claims 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 claims 1
- 125000004450 alkenylene group Chemical group 0.000 claims 1
- 125000005078 alkoxycarbonylalkyl group Chemical group 0.000 claims 1
- 125000005250 alkyl acrylate group Chemical group 0.000 claims 1
- 229910052787 antimony Inorganic materials 0.000 claims 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 125000002619 bicyclic group Chemical group 0.000 claims 1
- 125000006309 butyl amino group Chemical group 0.000 claims 1
- 239000004202 carbamide Substances 0.000 claims 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N carbonic acid monoamide Natural products NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 125000002993 cycloalkylene group Chemical group 0.000 claims 1
- WJTCGQSWYFHTAC-UHFFFAOYSA-N cyclooctane Chemical group C1CCCCCCC1 WJTCGQSWYFHTAC-UHFFFAOYSA-N 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 150000004677 hydrates Chemical class 0.000 claims 1
- 229930195733 hydrocarbon Natural products 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 229910052751 metal Inorganic materials 0.000 claims 1
- 229910000000 metal hydroxide Inorganic materials 0.000 claims 1
- 150000004692 metal hydroxides Chemical class 0.000 claims 1
- 229910044991 metal oxide Inorganic materials 0.000 claims 1
- 150000004706 metal oxides Chemical class 0.000 claims 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims 1
- BAQLUVXNKOTTHU-UHFFFAOYSA-N metofenazate Chemical compound COC1=C(OC)C(OC)=CC(C(=O)OCCN2CCN(CCCN3C4=CC(Cl)=CC=C4SC4=CC=CC=C43)CC2)=C1 BAQLUVXNKOTTHU-UHFFFAOYSA-N 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 125000000466 oxiranyl group Chemical group 0.000 claims 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims 1
- 239000010452 phosphate Substances 0.000 claims 1
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical class [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 claims 1
- 229920001155 polypropylene Polymers 0.000 claims 1
- 150000003254 radicals Chemical class 0.000 claims 1
- 229920006395 saturated elastomer Polymers 0.000 claims 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 claims 1
- KJAMZCVTJDTESW-UHFFFAOYSA-N tiracizine Chemical compound C1CC2=CC=CC=C2N(C(=O)CN(C)C)C2=CC(NC(=O)OCC)=CC=C21 KJAMZCVTJDTESW-UHFFFAOYSA-N 0.000 claims 1
- 239000004711 α-olefin Substances 0.000 claims 1
- 230000002401 inhibitory effect Effects 0.000 abstract 2
- 229940058905 antimony compound for treatment of leishmaniasis and trypanosomiasis Drugs 0.000 abstract 1
- 150000001463 antimony compounds Chemical class 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 239000003063 flame retardant Substances 0.000 abstract 1
- 230000005764 inhibitory process Effects 0.000 abstract 1
- 125000005647 linker group Chemical group 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 0 CC1C(*)C(C)C(*)C(C)(C)C1 Chemical compound CC1C(*)C(C)C(*)C(C)(C)C1 0.000 description 2
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3477—Six-membered rings
- C08K5/3492—Triazines
- C08K5/34926—Triazines also containing heterocyclic groups other than triazine groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0066—Flame-proofing or flame-retarding additives
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring
- C08K5/3432—Six-membered rings
- C08K5/3435—Piperidines
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Paper (AREA)
- Printing Methods (AREA)
- Hydrogenated Pyridines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US5133197P | 1997-06-30 | 1997-06-30 | |
| US60/051331 | 1997-06-30 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU2000102671A RU2000102671A (ru) | 2002-10-27 |
| RU2207352C2 true RU2207352C2 (ru) | 2003-06-27 |
Family
ID=21970653
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2000102671/04A RU2207352C2 (ru) | 1997-06-30 | 1998-06-25 | Способ замедления горения полимерного субстрата и композиция ингибитора горения |
Country Status (12)
| Country | Link |
|---|---|
| EP (2) | EP1462481B1 (https=) |
| JP (1) | JP4378574B2 (https=) |
| KR (1) | KR100540156B1 (https=) |
| CN (1) | CN1178978C (https=) |
| AU (1) | AU735643B2 (https=) |
| BR (1) | BR9810957A (https=) |
| CA (1) | CA2292598C (https=) |
| DE (2) | DE69841728D1 (https=) |
| ES (1) | ES2227855T3 (https=) |
| RU (1) | RU2207352C2 (https=) |
| TW (1) | TW480276B (https=) |
| WO (1) | WO1999000450A1 (https=) |
Families Citing this family (86)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6309987B1 (en) * | 1998-04-20 | 2001-10-30 | Bba Nonwovens Simpsonville, Inc. | Nonwoven fabric having both UV stability and flame retardancy |
| EP1235863B1 (en) * | 1999-12-09 | 2005-01-26 | Ciba SC Holding AG | Use of an additive composition for increasing the storage stability of ethylenically unsaturated resins |
| JP2004083913A (ja) * | 2000-04-06 | 2004-03-18 | Mitsubishi Rayon Co Ltd | 難燃性ポリプロピレンフィルム |
| JP3540759B2 (ja) | 2000-04-06 | 2004-07-07 | 三菱レイヨン株式会社 | 難燃性ポリプロピレン繊維及びその製造方法 |
| JP3822046B2 (ja) * | 2000-10-11 | 2006-09-13 | 大和紡績株式会社 | 繊維およびその繊維組成物 |
| JP2002121333A (ja) * | 2000-10-13 | 2002-04-23 | Daiwabo Co Ltd | ポリオレフィン樹脂成形物及びそれからなるフィルム |
| TWI273115B (en) * | 2000-12-12 | 2007-02-11 | Ciba Sc Holding Ag | Improved weatherability of flame retardant polyolefin |
| GB2386901B (en) * | 2000-12-12 | 2004-03-31 | Ciba Sc Holding Ag | Improved weatherability of flame retardant polyolefin |
| JP2002322322A (ja) † | 2001-02-27 | 2002-11-08 | Bromine Compounds Ltd | 難燃性ポリオレフィン組成物 |
| DE60205734T2 (de) * | 2001-03-20 | 2006-03-09 | Ciba Speciality Chemicals Holding Inc. | Flammhemmende zusammensetzungen |
| US6465645B1 (en) | 2001-04-17 | 2002-10-15 | Ciba Specialty Chemicals Corporation | Long chain hindered amines and compositions stabilized therewith |
| JP3679738B2 (ja) * | 2001-07-16 | 2005-08-03 | 三菱レイヨン株式会社 | 難燃性ポリプロピレン繊維及びその製造方法 |
| US6822023B2 (en) * | 2001-12-03 | 2004-11-23 | Kaneka Corporation | Flame retardant polyolefin resin pre-expanded particles and in-mold foamed articles prepared therefrom |
| CN1602334A (zh) * | 2001-12-10 | 2005-03-30 | 西巴特殊化学品控股有限公司 | 阻燃剂组合物 |
| KR101029863B1 (ko) | 2001-12-21 | 2011-04-18 | 시바 홀딩 인코포레이티드 | 신규한 난연제 화합물 |
| JP2003251771A (ja) * | 2002-02-28 | 2003-09-09 | Hagihara Industries Inc | ポリオレフィン防炎性ラミネートシート |
| JP4091317B2 (ja) * | 2002-02-28 | 2008-05-28 | 萩原工業株式会社 | 光透過性を有するクロスシート |
| JP2004315544A (ja) * | 2002-02-28 | 2004-11-11 | Hagihara Industries Inc | ポリオレフィンフイルムまたはラミネートシート |
| JP2003251748A (ja) * | 2002-02-28 | 2003-09-09 | Hagihara Industries Inc | 膜材料ラミネートシート |
| JP2003251767A (ja) * | 2002-02-28 | 2003-09-09 | Hagihara Industries Inc | 不織布補強用ポリオレフィンクロスシート |
| JP4009117B2 (ja) * | 2002-03-06 | 2007-11-14 | 大和紡績株式会社 | オレフィン複合シートおよび強化複合不織布 |
| US7323502B2 (en) * | 2002-03-12 | 2008-01-29 | Ciba Specialty Chemicals Corporation | Flame retardant compositions |
| JP2004000173A (ja) * | 2002-03-28 | 2004-01-08 | Hagihara Industries Inc | 防草シート |
| JP3895207B2 (ja) * | 2002-03-29 | 2007-03-22 | 大和紡績株式会社 | 難燃性ポリオレフィン繊維およびこれを用いた繊維組成物と繊維積層体 |
| CA2479946A1 (en) * | 2002-04-10 | 2003-10-16 | Ciba Specialty Chemicals Holding Inc. | Flame retardant coatings |
| JP4324940B2 (ja) * | 2002-04-17 | 2009-09-02 | チバ ホールディング インコーポレーテッド | ヒドロキシルアミンエステル含有難燃性ポリマー組成物 |
| JP2003313737A (ja) * | 2002-04-24 | 2003-11-06 | Hagihara Industries Inc | パイル糸 |
| JP2004019074A (ja) * | 2002-06-19 | 2004-01-22 | Hagihara Industries Inc | 防虫網 |
| JP4016123B2 (ja) * | 2002-07-22 | 2007-12-05 | 平岡織染株式会社 | 難燃化ポリプロピレン系樹脂膜材 |
| JP2006501340A (ja) * | 2002-10-03 | 2006-01-12 | チバ スペシャルティ ケミカルズ ホールディング インコーポレーテッド | 難燃性組成物 |
| JP2004131869A (ja) * | 2002-10-10 | 2004-04-30 | Mitsubishi Rayon Co Ltd | 難燃性を有するポリプロピレン系熱接着性複合繊維及びその製造方法 |
| MY139230A (en) * | 2002-10-17 | 2009-08-28 | Ciba Holding Inc | Flame retardant polymeric electrical parts |
| US7109260B2 (en) * | 2002-10-17 | 2006-09-19 | Ciba Specialty Chemicals Corporation | Flame retardant compositions |
| CN100352852C (zh) * | 2002-10-17 | 2007-12-05 | 西巴特殊化学品控股有限公司 | 阻燃聚合物电气部件 |
| US7138448B2 (en) * | 2002-11-04 | 2006-11-21 | Ciba Specialty Chemicals Corporation | Flame retardant compositions |
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Also Published As
| Publication number | Publication date |
|---|---|
| WO1999000450A1 (en) | 1999-01-07 |
| EP1462481B1 (en) | 2010-06-16 |
| DE69826477T2 (de) | 2005-11-17 |
| EP1462481A3 (en) | 2004-10-13 |
| CA2292598A1 (en) | 1999-01-07 |
| DE69826477D1 (de) | 2004-10-28 |
| DE69841728D1 (de) | 2010-07-29 |
| CN1261904A (zh) | 2000-08-02 |
| AU8174998A (en) | 1999-01-19 |
| AU735643B2 (en) | 2001-07-12 |
| EP0996669B1 (en) | 2004-09-22 |
| KR100540156B1 (ko) | 2005-12-29 |
| CA2292598C (en) | 2008-03-18 |
| EP0996669A1 (en) | 2000-05-03 |
| ES2227855T3 (es) | 2005-04-01 |
| JP2002507238A (ja) | 2002-03-05 |
| JP4378574B2 (ja) | 2009-12-09 |
| TW480276B (en) | 2002-03-21 |
| EP1462481A2 (en) | 2004-09-29 |
| CN1178978C (zh) | 2004-12-08 |
| BR9810957A (pt) | 2000-09-26 |
| KR20010014333A (ko) | 2001-02-26 |
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