Fire-resistant polymeric composition
专利摘要:
Disclosed is a self-extinguishing polystyrenic composition comprising a polystyrenic resin, a fire-retardant amount of a halogenated organic fire-retardant agent and a benzotriazolic compound having the formula <IMAGE> wherein R1 is H or -CH3 and R2 is H or -CH2N(R3)2 wherein R3 is H, an alkyl radical containing from about 1 to 12 carbon atoms or -CH2 CH2 OH, in an amount between about 1 and 50% of the weight of said fire-retardant agent. 公开号:SU1077574A3 申请号:SU802862208 申请日:1980-01-02 公开日:1984-02-29 发明作者:Мари Бертран Жан-Ноэль 申请人:Лябофина С.А. (Фирма); IPC主号:
专利说明:
vj Compound B R tCH3 3f - R -H, R2 -CH, N (R Compound C o R Compound DRH; R - :: H2N (R with R -CH2CH20H) Samples are obtained from the composition and tested for self-extinguishing. The average burning time is , s: Without an additive With compound A 1.60 With compound B 1.02 With compound C 0.51 With compound D 0.53 EXAMPLE 2 Preparing several mixtures containing 100 parts by weight of crystalline polystyrene 0.05 parts by weight of BHT, 0.035 parts by weight of zinc stearate and 0.75 parts by weight of flame retardant. Some mixtures are also added with 0.20 parts by weight of benotriazole. Samples are prepared from the composition and tested for self-extinguishing Table 1 shows the dependence of the self-extinguishing time qT of the used flame retardant Table The average time of burning is ANTIPYRENE, with benzot without triazole benzoazole Tetrabromide-acetylene 8,21 Dibromotetrachloroethane 15,75 Tetrachloroethane 60, 0 Example 3. A mixture is prepared, holding 100 wt.h. crystalline polystyrene, 0.05 parts by weight of BHT, 0.035 parts by weight of zinc stearate, 3.75 May, including pentabrommonochlorocyclohexane and 1.75 parts by weight benzotriaeol Samples are prepared from the composition and tested for self-extinguishing. . The average burning time is 0.42 s. EXAMPLE 4 Preparing formulations based on 100 wt.h. polystyrene with enhanced impact strength (with uchuch); 10 wt.h. flame retardant and 5. wt.h. antimony trioxide. To a portion of these formulations, 2 mab isotriazole is also added. Samples are prepared from the composition and tested for self-extinguishing. PRI me R 5. A plate is molded on the basis of expandable polystyrene beads. la, containing pentane as a substance that promotes swelling. In the experiment, 1.5 wt.h. pentabromyl and cyclohexane and 0.2 wt.h. benzotriazole compounds corresponding to formula I / where R is H, R (R), where R. Samples are prepared from the composition and tested for self-extinguishing. The average burning time is 8., O c. In another experiment without a benzotriazole compound, the average burning time is 17.0 seconds. Example b ... Preparing a composition based on 100 wt.h. crystalline polystyrene, 5 wt.h. chlorinated paraffin (having an average of 25 carbon atoms, the chlorine content of 70%), 0.1 wt.h. BHT; o, 035 wt.h, zinc stearate and 0.2 wt.h. benzotriazole. Samples are prepared from the composition and tested for self-extinguishing. The average burning time is 22.43 seconds. Such a composition, which does not contain benzotriazole, has an average Burn time above 60 s, Example 7. A composition based on 100 wt.h. acrylonitrile butadiene styrene resin (ABS) (containing 7% butadiene and 17% acrylonitrile), 12 parts by weight, decabromobiphenyl oxide, 5 parts by weight, SbjO and 2% by weight, of a compound of benzotriazole having formula I in which R represents -H R represents -CHjN (,). Samples are prepared from the composition and tested for self-extinguishing. The average burning time is 1.23 seconds. This composition, which does not contain a benzotriazole compound, has an average burning time of 3.48 seconds. Example. (Prototype). Prepare a mixture of 100 mash, high impact polystyrene with 10 mach. decabromobiphenyl, 0.2 mph. lauric acid diethanopamide and 5 May.4. antimony trioxide. Samples are prepared from the composition and tested for self-extinguishing. The burning time is 0.7 s. The data given in examples 1-7 show that adding to the known organic, chlorine and / or bromine-containing fire retardants of the 1, 2,3-benzotriazole derivative according to the invention improves the self-damping effect by a factor of 2-20. Comparison of similar compositions according to the invention (Example 4, flame retardant - Decabromobiphenyl) and the prototype (Example 8) shows that the composition according to the invention is more effective (1.4 times more. Thus, the composition of the invention provides a more fire resistant material.
权利要求:
Claims (1) [1] 1. FIRE-RESISTANT POLYMER COMPOSITION, including a styrene polymer, an organic chlorine and / or bromine-containing flame retardant and an organic nitrogen-containing compound, characterized in that, in order to increase the effect of self-extinguishing, it contains a 1,2-derivative as an organic nitrogen-containing compound 3-Beneotriazole General Formula R 1 i * where R'- - H, —CH, J R 2 - H, -CH 2 N (R *) 1, R '- C m th 41 , -CH 2 CH g OH, in the following ratio of components, parts, parts by weight: Styrene polymer Organic chlorine and / or bromine-containing flame retardant Derived 1,2,3benzotriazole 2. The composition according to p. repenting in that it additionally contains antimony trioxide in an amount of 5 parts by weight 100 IN 0.75-12.0 0.2-2.0 1, about aphids SU, „, 1077574
类似技术:
公开号 | 公开日 | 专利标题 US5760115A|1998-06-02|Fire-retardant polymer composition SE425503B|1982-10-04|BINDING COMPOSITION INCLUDING A SALT OF A TEREFTALAMIDE AS A GELING AGENT SU1077574A3|1984-02-29|Fire-resistant polymeric composition US4173561A|1979-11-06|Flame retardant polymer composition US3271333A|1966-09-06|Self-extinguishing alkenyl aromatic polymers US3004935A|1961-10-17|Self-extinguishing alkenyl polymer compositions containing polybromo cyclohexanes US4134878A|1979-01-16|Novel organotin stabilizer compositions and polyvinyl resins stabilized therewith CA1106990A|1981-08-11|Fire-retardant non-drip elastoplastic polyurethane compositions US2760947A|1956-08-28|Self-extinguishing alkenyl polymer compositions containing bromochloro compounds US4144288A|1979-03-13|Sodium tetraborate pentahydrate as a smoke suppressant for styrenic resins US3269962A|1966-08-30|Self-extinguishing polymer composition containing a halide and a hydrazone US4179298A|1979-12-18|Flame retardant intumescent polyamides US4293464A|1981-10-06|Phosphine oxide flame retarded, rubber-modified, polyphenylene ether resin compositions US4378440A|1983-03-29|Self-extinguishing polystyrenic compositions and process for their preparation US4024092A|1977-05-17|Polymer compositions containing stilbene halide additives US4098759A|1978-07-04|Bromine-containing cyclic phosphonic acid esters US4224217A|1980-09-23|Combustion resistant aromatic polymers containing char-forming benzyl and/or allyl moieties US4725638A|1988-02-16|Flame retardant polymer compositions US4181671A|1980-01-01|Novel organotin stabilizer compositions US3551360A|1970-12-29|Self-extinguishing styrene polymer compositions CA1116628A|1982-01-19|Brominated phenyl benzenesulfonatesas flame-retardant US4059560A|1977-11-22|Smoke and flame retarded styrene polymers US4057531A|1977-11-08|Fire retardant polystyrene US4297475A|1981-10-27|Flame retardant intumescent polyamide from haloamide US4178330A|1979-12-11|Haloaryl halobenzenesulfonate flame retardants
同族专利:
公开号 | 公开日 NL186582C|1991-01-02| CA1153843A|1983-09-13| JPH0255453B2|1990-11-27| FR2449704B1|1983-06-10| NO159450B|1988-09-19| IT7928298D0|1979-12-21| GB2042561A|1980-09-24| FR2449704A1|1980-09-19| JPS55116744A|1980-09-08| DE3000608A1|1980-08-28| SE7910651L|1980-08-27| DE3000608C2|1991-03-21| NO159450C|1988-12-28| CS222685B2|1983-07-29| GB2042561B|1983-03-23| BE881839A|1980-06-16| NO794119L|1980-08-27| NL186582B|1990-08-01| US4230821A|1980-10-28| NL7909194A|1980-08-28| IT1127309B|1986-05-21|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题 DE4301601A1|1993-01-22|1994-07-28|Chemie Linz Deutschland|Fire resistant plastics|NL265130A|1960-05-31| US3324076A|1963-11-04|1967-06-06|Dow Chemical Co|Alkenyl aromatic polymers containing halogen compounds as flame retardants and triphosphate or triborate as corrosion inhibitor| DE2046795B2|1970-09-23|1975-05-07|Chemische Fabrik Kalk Gmbh, 5000 Koeln|Self-extinguishing molding compounds based on acrylonitrile-butadiene-styrene polymers| US3828003A|1970-10-26|1974-08-06|Nippon Oils & Fats Co Ltd|Flame resistant polymer compositions| FR2120813A5|1970-12-31|1972-08-18|Huels Chemische Werke Ag| US3981856A|1974-03-07|1976-09-21|Princeton Polymer Laboratories, Incorporated|Degradable hydrocarbon polymers containing a metal compound and a benzotriazole| DE2314544A1|1973-03-23|1974-10-10|Basf Ag|FINE PART, EXPANDABLE, FLAME RESISTANT STYRENE POLYMERIZED WITH GOOD PROCESSABILITY| JPS5625955B2|1973-12-27|1981-06-16| CS210623B2|1974-07-12|1982-01-29|Labofina Sa|Polymere heat resistant mixture| US4033916A|1974-10-17|1977-07-05|Uniroyal Inc.|Ternary flame-retarded compositions including iron oxide| US4024092A|1975-12-10|1977-05-17|Foster Grant Co., Inc.|Polymer compositions containing stilbene halide additives| US4067930A|1976-11-26|1978-01-10|Cities Service Company|Flame-retardant composition| US4087399A|1977-07-11|1978-05-02|Toray Silicone Company, Ltd.|Self-extinguishing silicone elastomer compositions|US4619954A|1984-06-22|1986-10-28|Sequentia, Incorporated|Fiberglass reinforced plastic sheet material with fire retardant filler| JPH04314749A|1991-04-12|1992-11-05|Dai Ichi Kogyo Seiyaku Co Ltd|Flame-retardant styrene resin composition| US6518468B1|1994-09-16|2003-02-11|Albemarle Corporation|Bromination process| TW455603B|1996-12-23|2001-09-21|Ciba Sc Holding Ag|Light-stabilised flameproof styrene homopolymers and copolymers| US6743825B1|2001-08-03|2004-06-01|Albemarle Corporation|Polyalkane additives and methods for their preparation and use| KR100493957B1|2001-12-27|2005-06-08|제일모직주식회사|Acrylonitrile-Butadiene-Styrene Flame Retardant Resin Composition with Good Impact Strength, Flammability and Easy Colorability|
法律状态:
优先权:
[返回顶部]
申请号 | 申请日 | 专利标题 US06/015,399|US4230821A|1979-02-26|1979-02-26|Fire-retardant polystyrenic compositions| 相关专利
Sulfonates, polymers, resist compositions and patterning process
Washing machine
Washing machine
Device for fixture finishing and tension adjusting of membrane
Structure for Equipping Band in a Plane Cathode Ray Tube
Process for preparation of 7 alpha-carboxyl 9, 11-epoxy steroids and intermediates useful therein an
国家/地区
|