CA1145083A - Fire-retardant polystyrenic compositions - Google Patents
Fire-retardant polystyrenic compositionsInfo
- Publication number
- CA1145083A CA1145083A CA000345834A CA345834A CA1145083A CA 1145083 A CA1145083 A CA 1145083A CA 000345834 A CA000345834 A CA 000345834A CA 345834 A CA345834 A CA 345834A CA 1145083 A CA1145083 A CA 1145083A
- Authority
- CA
- Canada
- Prior art keywords
- carbon atoms
- alkyl radical
- composition
- fire
- compound
- 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.)
- Expired
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 53
- 239000003063 flame retardant Substances 0.000 title claims abstract description 39
- -1 nitrogen-containing organic compound Chemical class 0.000 claims abstract description 61
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 44
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 32
- 229920005989 resin Polymers 0.000 claims abstract description 20
- 239000011347 resin Substances 0.000 claims abstract description 20
- 150000003868 ammonium compounds Chemical class 0.000 claims abstract description 19
- 239000004793 Polystyrene Substances 0.000 claims description 16
- 229920002223 polystyrene Polymers 0.000 claims description 16
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 13
- 229910052794 bromium Inorganic materials 0.000 claims description 9
- 229910052801 chlorine Inorganic materials 0.000 claims description 9
- 229910000410 antimony oxide Inorganic materials 0.000 claims description 7
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 claims description 7
- SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical compound [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 claims description 6
- REZZEXDLIUJMMS-UHFFFAOYSA-M dimethyldioctadecylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC REZZEXDLIUJMMS-UHFFFAOYSA-M 0.000 claims description 6
- 239000004664 distearyldimethylammonium chloride (DHTDMAC) Substances 0.000 claims description 6
- AUTSLLHNWAZVLE-UHFFFAOYSA-N 1,1,2,2,3-pentabromo-3-chlorocyclohexane Chemical compound ClC1(Br)CCCC(Br)(Br)C1(Br)Br AUTSLLHNWAZVLE-UHFFFAOYSA-N 0.000 claims description 5
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 5
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 claims description 5
- 239000000194 fatty acid Substances 0.000 claims description 5
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 claims description 4
- 229920001890 Novodur Polymers 0.000 claims description 4
- 125000002947 alkylene group Chemical group 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- WLCFKPHMRNPAFZ-UHFFFAOYSA-M didodecyl(dimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCC WLCFKPHMRNPAFZ-UHFFFAOYSA-M 0.000 claims description 4
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 4
- 150000003335 secondary amines Chemical class 0.000 claims description 4
- 125000004079 stearyl 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])C([H])([H])C([H])([H])C([H])([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 description 4
- 150000003512 tertiary amines Chemical class 0.000 claims description 4
- QXSZNDIIPUOQMB-UHFFFAOYSA-N 1,1,2,2-tetrabromoethane Chemical group BrC(Br)C(Br)Br QXSZNDIIPUOQMB-UHFFFAOYSA-N 0.000 claims description 3
- GGMQZPIDPNAGFP-UHFFFAOYSA-N 1,1-dibromo-1,2,2,2-tetrachloroethane Chemical compound ClC(Cl)(Cl)C(Cl)(Br)Br GGMQZPIDPNAGFP-UHFFFAOYSA-N 0.000 claims description 3
- CAYGQBVSOZLICD-UHFFFAOYSA-N hexabromobenzene Chemical compound BrC1=C(Br)C(Br)=C(Br)C(Br)=C1Br CAYGQBVSOZLICD-UHFFFAOYSA-N 0.000 claims description 3
- BNIXVQGCZULYKV-UHFFFAOYSA-N pentachloroethane Chemical compound ClC(Cl)C(Cl)(Cl)Cl BNIXVQGCZULYKV-UHFFFAOYSA-N 0.000 claims description 3
- HGRZLIGHKHRTRE-UHFFFAOYSA-N 1,2,3,4-tetrabromobutane Chemical compound BrCC(Br)C(Br)CBr HGRZLIGHKHRTRE-UHFFFAOYSA-N 0.000 claims description 2
- QAQSNXHKHKONNS-UHFFFAOYSA-N 1-ethyl-2-hydroxy-4-methyl-6-oxopyridine-3-carboxamide Chemical compound CCN1C(O)=C(C(N)=O)C(C)=CC1=O QAQSNXHKHKONNS-UHFFFAOYSA-N 0.000 claims description 2
- RUHLNQWHGYWOBA-UHFFFAOYSA-N C(CCCCCCCCCCCCCCCCC)OS(=O)(=O)[O-].C(CCCCC)[NH+](C)C Chemical compound C(CCCCCCCCCCCCCCCCC)OS(=O)(=O)[O-].C(CCCCC)[NH+](C)C RUHLNQWHGYWOBA-UHFFFAOYSA-N 0.000 claims description 2
- XCSXSYLKDIICBU-UHFFFAOYSA-M [[2,3-bis(2-methylpropyl)phenyl]-ethoxy-phenoxymethyl]-ethyl-dimethylazanium;chloride;hydrate Chemical compound O.[Cl-].C=1C=CC(CC(C)C)=C(CC(C)C)C=1C([N+](C)(C)CC)(OCC)OC1=CC=CC=C1 XCSXSYLKDIICBU-UHFFFAOYSA-M 0.000 claims description 2
- 150000008051 alkyl sulfates Chemical class 0.000 claims description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- XRWMGCFJVKDVMD-UHFFFAOYSA-M didodecyl(dimethyl)azanium;bromide Chemical compound [Br-].CCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCC XRWMGCFJVKDVMD-UHFFFAOYSA-M 0.000 claims description 2
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- HKUFIYBZNQSHQS-UHFFFAOYSA-N n-octadecyloctadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCNCCCCCCCCCCCCCCCCCC HKUFIYBZNQSHQS-UHFFFAOYSA-N 0.000 claims description 2
- SFVFIFLLYFPGHH-UHFFFAOYSA-M stearalkonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 SFVFIFLLYFPGHH-UHFFFAOYSA-M 0.000 claims description 2
- SWZDQOUHBYYPJD-UHFFFAOYSA-N tridodecylamine Chemical compound CCCCCCCCCCCCN(CCCCCCCCCCCC)CCCCCCCCCCCC SWZDQOUHBYYPJD-UHFFFAOYSA-N 0.000 claims description 2
- 125000005526 alkyl sulfate group Chemical group 0.000 claims 4
- 229920001577 copolymer Polymers 0.000 claims 2
- 229940000425 combination drug Drugs 0.000 claims 1
- 229940126214 compound 3 Drugs 0.000 claims 1
- AICOOMRHRUFYCM-ZRRPKQBOSA-N oxazine, 1 Chemical compound C([C@@H]1[C@H](C(C[C@]2(C)[C@@H]([C@H](C)N(C)C)[C@H](O)C[C@]21C)=O)CC1=CC2)C[C@H]1[C@@]1(C)[C@H]2N=C(C(C)C)OC1 AICOOMRHRUFYCM-ZRRPKQBOSA-N 0.000 claims 1
- 239000012188 paraffin wax Substances 0.000 claims 1
- 150000001412 amines Chemical class 0.000 abstract description 4
- 150000001408 amides Chemical class 0.000 abstract description 3
- 150000001875 compounds Chemical class 0.000 description 20
- 230000002195 synergetic effect Effects 0.000 description 16
- 238000002485 combustion reaction Methods 0.000 description 14
- 239000000460 chlorine Substances 0.000 description 5
- 239000004794 expanded polystyrene Substances 0.000 description 5
- 239000011324 bead Substances 0.000 description 4
- 239000013078 crystal Substances 0.000 description 4
- 229920001971 elastomer Polymers 0.000 description 4
- 150000003254 radicals Chemical class 0.000 description 4
- 229940044603 styrene Drugs 0.000 description 4
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 4
- 239000004604 Blowing Agent Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 125000004429 atom Chemical group 0.000 description 3
- 229920005669 high impact polystyrene Polymers 0.000 description 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 3
- 150000002894 organic compounds Chemical class 0.000 description 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 2
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 230000001627 detrimental effect Effects 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920000638 styrene acrylonitrile Polymers 0.000 description 2
- AQPHBYQUCKHJLT-UHFFFAOYSA-N 1,2,3,4,5-pentabromo-6-(2,3,4,5,6-pentabromophenyl)benzene Chemical group BrC1=C(Br)C(Br)=C(Br)C(Br)=C1C1=C(Br)C(Br)=C(Br)C(Br)=C1Br AQPHBYQUCKHJLT-UHFFFAOYSA-N 0.000 description 1
- UZOSVZSBPTTWIG-UHFFFAOYSA-N 1,2,3,4,5-pentabromo-6-chlorocyclohexane Chemical compound ClC1C(Br)C(Br)C(Br)C(Br)C1Br UZOSVZSBPTTWIG-UHFFFAOYSA-N 0.000 description 1
- KNENSDLFTGIERH-UHFFFAOYSA-N 2,2,4,4-tetramethyl-3-phenylpentan-3-ol Chemical compound CC(C)(C)C(O)(C(C)(C)C)C1=CC=CC=C1 KNENSDLFTGIERH-UHFFFAOYSA-N 0.000 description 1
- CQJATPXNOIKBGO-UHFFFAOYSA-N 3-bromo-3,4,4,5,5,6-hexachlorocyclohexene Chemical compound ClC1C=CC(Cl)(Br)C(Cl)(Cl)C1(Cl)Cl CQJATPXNOIKBGO-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000007824 aliphatic compounds Chemical class 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 230000008033 biological extinction Effects 0.000 description 1
- ZCILODAAHLISPY-UHFFFAOYSA-N biphenyl ether Natural products C1=C(CC=C)C(O)=CC(OC=2C(=CC(CC=C)=CC=2)O)=C1 ZCILODAAHLISPY-UHFFFAOYSA-N 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 150000001649 bromium compounds Chemical class 0.000 description 1
- WHHGLZMJPXIBIX-UHFFFAOYSA-N decabromodiphenyl ether Chemical compound BrC1=C(Br)C(Br)=C(Br)C(Br)=C1OC1=C(Br)C(Br)=C(Br)C(Br)=C1Br WHHGLZMJPXIBIX-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 229920006248 expandable polystyrene Polymers 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000012757 flame retardant agent Substances 0.000 description 1
- 229940083124 ganglion-blocking antiadrenergic secondary and tertiary amines Drugs 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 239000004797 high-impact polystyrene Substances 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 150000002896 organic halogen compounds Chemical class 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0014—Use of organic additives
- C08J9/0028—Use of organic additives containing nitrogen
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2325/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Derivatives of such polymers
- C08J2325/02—Homopolymers or copolymers of hydrocarbons
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US2225779A | 1979-03-20 | 1979-03-20 | |
| US22,257 | 1979-03-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1145083A true CA1145083A (en) | 1983-04-19 |
Family
ID=21808670
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000345834A Expired CA1145083A (en) | 1979-03-20 | 1980-02-18 | Fire-retardant polystyrenic compositions |
Country Status (12)
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3047443A1 (de) * | 1980-12-17 | 1982-07-22 | Bayer Ag, 5090 Leverkusen | Gegen thermolyse stabilisierte formmassen mit geringem monomerengehalt |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE817625A (fr) * | 1974-07-12 | 1974-11-04 | Compositions polystyreniques ignifuges. | |
| CS210623B2 (en) * | 1974-07-12 | 1982-01-29 | Labofina Sa | Polymere heat resistant mixture |
-
1980
- 1980-02-11 GB GB8004433A patent/GB2048276B/en not_active Expired
- 1980-02-18 CA CA000345834A patent/CA1145083A/en not_active Expired
- 1980-02-28 SU SU802888301A patent/SU1097200A3/ru active
- 1980-02-29 NL NLAANVRAGE8001248,A patent/NL190163C/xx not_active IP Right Cessation
- 1980-03-10 DE DE19803009065 patent/DE3009065A1/de active Granted
- 1980-03-10 FR FR8005297A patent/FR2451928B1/fr not_active Expired
- 1980-03-12 IT IT20521/80A patent/IT1140778B/it active
- 1980-03-14 BE BE0/199810A patent/BE882241A/fr not_active IP Right Cessation
- 1980-03-17 SE SE8002057A patent/SE8002057L/xx unknown
- 1980-03-18 NO NO800768A patent/NO162077C/no unknown
- 1980-03-18 JP JP3351880A patent/JPS55125140A/ja active Granted
- 1980-03-19 CS CS801902A patent/CS226409B2/cs unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NL190163B (nl) | 1993-06-16 |
| NO800768L (no) | 1980-09-22 |
| NL8001248A (nl) | 1980-09-23 |
| JPH0255454B2 (enrdf_load_html_response) | 1990-11-27 |
| GB2048276B (en) | 1983-03-30 |
| FR2451928A1 (fr) | 1980-10-17 |
| GB2048276A (en) | 1980-12-10 |
| IT1140778B (it) | 1986-10-10 |
| DE3009065A1 (de) | 1980-10-02 |
| NO162077B (no) | 1989-07-24 |
| SU1097200A3 (ru) | 1984-06-07 |
| DE3009065C2 (enrdf_load_html_response) | 1993-04-15 |
| IT8020521A0 (it) | 1980-03-12 |
| JPS55125140A (en) | 1980-09-26 |
| NO162077C (no) | 1989-11-01 |
| FR2451928B1 (fr) | 1986-08-01 |
| BE882241A (fr) | 1980-07-01 |
| CS226409B2 (en) | 1984-03-19 |
| NL190163C (nl) | 1993-11-16 |
| SE8002057L (sv) | 1980-09-21 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4092281A (en) | Fire retardant polystyrenic compositions | |
| US3207731A (en) | Self-extinguishing alkenyl aromatic polymeric compositions containing polybromophenyl acrylates and dibromocyclopropyl styrenes | |
| US6908949B2 (en) | Foamable interpolymer resin particles containing limonene as a blowing aid | |
| US4476267A (en) | High impact polystyrene containing halophenoxyalkylsilane flame retardant | |
| US4108943A (en) | Rubber modified fire retardant polymer compositions | |
| US3271333A (en) | Self-extinguishing alkenyl aromatic polymers | |
| US3819547A (en) | Self-extinguishing polymer compositions containing hexabromo-2-butene | |
| EP0014764B1 (de) | Selbstverlöschende feinteilige expandierbare Styrolpolymerisate | |
| US4230821A (en) | Fire-retardant polystyrenic compositions | |
| US4359538A (en) | Fire-retardant polystyrenic compositions | |
| US3284544A (en) | Self-extinguishing alkenyl aromatic resins containing organic polysulfide | |
| CA1145083A (en) | Fire-retardant polystyrenic compositions | |
| US4430467A (en) | Self-extinguishing propylene polymer | |
| US3269962A (en) | Self-extinguishing polymer composition containing a halide and a hydrazone | |
| US3883615A (en) | Flame-retardant impact-resistant resin composition | |
| US3296340A (en) | Self-extinguishing alkenyl aromatic resins containing sulfenamides | |
| US3971758A (en) | Plastic compositions containing acrylonitrile-butadiene-styrene polymer and a bis-phenoxy flame retardant | |
| CA1113650A (en) | Finely divided expandable styrene polymers | |
| EP0103922B1 (en) | Self-extinguishing polycarbonate composition | |
| CA1116800A (en) | Self-extinguishing polystyrenic compositions and process for their preparation | |
| CA1067240A (en) | Smoke-and flame-retardant styrene/acrylonitrile/methyl methacrylate interpolymeric molding compositions | |
| JPS63117057A (ja) | 難燃性耐熱性芳香族ビニル系樹脂組成物 | |
| EP0013051B1 (en) | Thermoplastic moulding material and article prepared thereof | |
| US3892710A (en) | ABS plastic compositions containing halogenated aryl flame retardants | |
| US3883479A (en) | ABS plastic compositions containing bio-phenoxy flame retardants |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MKEX | Expiry |