DE1694001A1 - Selbsterloeschende Styrolpolymeren-Masse - Google Patents
Selbsterloeschende Styrolpolymeren-MasseInfo
- Publication number
- DE1694001A1 DE1694001A1 DE19681694001 DE1694001A DE1694001A1 DE 1694001 A1 DE1694001 A1 DE 1694001A1 DE 19681694001 DE19681694001 DE 19681694001 DE 1694001 A DE1694001 A DE 1694001A DE 1694001 A1 DE1694001 A1 DE 1694001A1
- Authority
- DE
- Germany
- Prior art keywords
- styrene
- ether
- polymer
- propane
- bromine
- 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
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 title claims description 38
- 229920000642 polymer Polymers 0.000 title claims description 29
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 23
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 claims description 17
- 150000002170 ethers Chemical class 0.000 claims description 11
- 150000001875 compounds Chemical class 0.000 claims description 9
- 239000001294 propane Substances 0.000 claims description 8
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 7
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 7
- 229910052794 bromium Inorganic materials 0.000 claims description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 125000003342 alkenyl group Chemical group 0.000 claims description 4
- 150000002989 phenols Chemical class 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- 125000005024 alkenyl aryl group Chemical group 0.000 claims description 2
- 125000001033 ether group Chemical group 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims description 2
- BPABLEVYTPZMOJ-UHFFFAOYSA-N 1,3-dibromonaphthalen-2-ol Chemical compound C1=CC=CC2=C(Br)C(O)=C(Br)C=C21 BPABLEVYTPZMOJ-UHFFFAOYSA-N 0.000 claims 1
- RZYQECXFRLRRJY-UHFFFAOYSA-N 2,6-dibromo-4-tert-butylphenol Chemical compound CC(C)(C)C1=CC(Br)=C(O)C(Br)=C1 RZYQECXFRLRRJY-UHFFFAOYSA-N 0.000 claims 1
- 238000004140 cleaning Methods 0.000 claims 1
- 238000005260 corrosion Methods 0.000 description 6
- 230000007797 corrosion Effects 0.000 description 6
- 239000003063 flame retardant Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 239000004793 Polystyrene Substances 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- 238000000354 decomposition reaction Methods 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 229920002223 polystyrene Polymers 0.000 description 4
- -1 2,3-dibromo-2-butenyl Chemical group 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 230000015556 catabolic process Effects 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 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 group 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 description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- 150000008378 aryl ethers Chemical class 0.000 description 2
- 125000001246 bromo group Chemical group Br* 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 150000004780 naphthols Chemical class 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- 239000005060 rubber Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 description 1
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 1
- XKZQKPRCPNGNFR-UHFFFAOYSA-N 2-(3-hydroxyphenyl)phenol Chemical compound OC1=CC=CC(C=2C(=CC=CC=2)O)=C1 XKZQKPRCPNGNFR-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- 241001476763 Einara Species 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 241000282320 Panthera leo Species 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 241001122767 Theaceae Species 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- SQHOHKQMTHROSF-UHFFFAOYSA-N but-1-en-2-ylbenzene Chemical compound CCC(=C)C1=CC=CC=C1 SQHOHKQMTHROSF-UHFFFAOYSA-N 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000002144 chemical decomposition reaction Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 239000011872 intimate mixture Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 238000005406 washing Methods 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
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/06—Ethers; Acetals; Ketals; Ortho-esters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/12—Polymerisation in non-solvents
- C08F2/16—Aqueous medium
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F279/00—Macromolecular compounds obtained by polymerising monomers on to polymers of monomers having two or more carbon-to-carbon double bonds as defined in group C08F36/00
- C08F279/02—Macromolecular compounds obtained by polymerising monomers on to polymers of monomers having two or more carbon-to-carbon double bonds as defined in group C08F36/00 on to polymers of conjugated dienes
-
- 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
- C08K5/04—Oxygen-containing compounds
- C08K5/13—Phenols; Phenolates
- C08K5/136—Phenols containing halogens
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L25/00—Compositions 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; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L9/00—Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
Landscapes
- 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)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US256109A US3372141A (en) | 1963-02-04 | 1963-02-04 | Self-extinguishing polystyrene resin compositions |
| AU32218/68A AU422568B2 (en) | 1963-02-04 | 1968-01-10 | Self-extinguishing polystrene resin compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1694001A1 true DE1694001A1 (de) | 1971-03-11 |
Family
ID=25622044
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19681694001 Pending DE1694001A1 (de) | 1963-02-04 | 1968-01-08 | Selbsterloeschende Styrolpolymeren-Masse |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US3372141A (enExample) |
| AU (1) | AU422568B2 (enExample) |
| BE (1) | BE708871A (enExample) |
| DE (1) | DE1694001A1 (enExample) |
| FR (1) | FR1550864A (enExample) |
| GB (1) | GB1211254A (enExample) |
| NL (1) | NL6800406A (enExample) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3883481A (en) * | 1966-10-28 | 1975-05-13 | Huels Chemische Werke Ag | Fire-retardant polyolefin compositions |
| US3666692A (en) * | 1970-02-24 | 1972-05-30 | Dow Chemical Co | Flame retardant polypropylene and polyurethane |
| US3962164A (en) * | 1970-09-23 | 1976-06-08 | Chemische Fabrik Kalk Gmbh | Self-extinguishing acrylonitrile-butadiene-styrene moulding composition |
| US3717609A (en) * | 1971-05-06 | 1973-02-20 | Hercules Inc | Flame retardant polymers |
| IT979365B (it) * | 1973-02-22 | 1974-09-30 | Montedison Spa | Procedimento per la produzione di particelle di polistirene espandibile per l ottenimento di corpi stampati a strutttura cellulare con elevate caratte ristiche |
| US4224217A (en) * | 1978-01-05 | 1980-09-23 | The Dow Chemical Company | Combustion resistant aromatic polymers containing char-forming benzyl and/or allyl moieties |
| US4578416A (en) * | 1982-08-31 | 1986-03-25 | Mobil Oil Corporation | Flame retardant high impact poly paramethylstyrene compositions |
| JPS61179249A (ja) * | 1985-02-05 | 1986-08-11 | Mitsui Toatsu Chem Inc | 難燃性スチレン系樹脂組成物 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3009888A (en) * | 1957-07-13 | 1961-11-21 | Basf Ag | Difficultly inflammable expandable styrene polymer containing an acetal or ether of 2, 3-dibromopropanol-1 and method of preparing same |
| DE1123823B (de) * | 1959-12-18 | 1962-02-15 | Huels Chemische Werke Ag | Schwer entflammbare Formmassen auf Basis von Polyolefinen |
-
1963
- 1963-02-04 US US256109A patent/US3372141A/en not_active Expired - Lifetime
-
1968
- 1968-01-02 BE BE708871D patent/BE708871A/xx unknown
- 1968-01-08 DE DE19681694001 patent/DE1694001A1/de active Pending
- 1968-01-10 AU AU32218/68A patent/AU422568B2/en not_active Expired
- 1968-01-10 GB GB0481/68A patent/GB1211254A/en not_active Expired
- 1968-01-11 NL NL6800406A patent/NL6800406A/xx unknown
- 1968-01-12 FR FR135783A patent/FR1550864A/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| GB1211254A (en) | 1970-11-04 |
| NL6800406A (enExample) | 1969-07-15 |
| US3372141A (en) | 1968-03-05 |
| BE708871A (enExample) | 1968-07-02 |
| AU3221868A (en) | 1969-07-17 |
| FR1550864A (enExample) | 1968-12-20 |
| AU422568B2 (en) | 1972-03-22 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1918069C3 (de) | Fasern und Folien aus Polyätherreste und Harntoffreste enthaltenden segmentierten Polyurethanen | |
| DE1694001A1 (de) | Selbsterloeschende Styrolpolymeren-Masse | |
| DE1201053B (de) | Halogenierte Cyclohexane enthaltende Styrol-polymerisate | |
| DE2120154C3 (de) | Stabilisierte Polymermischungen auf Basis von Polyphenylenäthern und Polystyrol | |
| DE2853884A1 (de) | Flammhemmende polycarbonat-zusammensetzung | |
| DE2854259C2 (de) | Stabilisierte Polycarbonatformmasse | |
| DE1669669A1 (de) | Polyestermaterial und Verfahren zu seiner Herstellung | |
| DE2520317A1 (de) | Statistische gemische halogenierter bisphenole mit halogenfreien bisphenolen sowie ein verfahren zu ihrer herstellung sowie ihre verwendung zur herstellung von hochmolekularen thermoplastischen polycarbonaten | |
| DE962831C (de) | Verfahren zum Stabilisieren von vinylidenchloridhaltigen Mischpolymerisaten | |
| DE2049358C3 (de) | Flammwidriges Polycarbonat | |
| DE2328517A1 (de) | Kunststoffzubereitungen | |
| DE1265409B (de) | Verfahren zum Stabilisieren von Polyolefinen | |
| DE1544882C3 (de) | Stabilisierte Spinnlösungen von Copolymerisaten des Acrylnitril mit Vinylidenchlorid | |
| US4175071A (en) | Titanium dioxide as a U.V. screen in fire retardant vinyl polymers | |
| DE1938014C (de) | 2,3-Dibrom-l,2,4-trichlor-butan und dessen Verwendung | |
| DE2937877A1 (de) | Flammwidrigesolycarbonat | |
| AT209884B (de) | Verfahren zur Stabilisierung chlorierter Kohlenwasserstoffe | |
| DE2202215C3 (de) | Mit organischen, fluoreszierenden Farbstoffen gefärbte Massen | |
| DE2818982C3 (de) | Di-(3,5-dicyclopentyl-4-hydroxybenzyl)sulfid und dessen Verwendung | |
| DE2164464A1 (de) | Polycarbonatzusammensetzung | |
| AT228494B (de) | Verfahren zum Vernetzen von Äthylenpolymeren | |
| DE2302230A1 (de) | Stabilisierung von kautschuk mit nickelkomplexen von thiobis(p-alkylphenolen) | |
| DE1198550B (de) | Stabilisierte Form- oder UEberzugsmassen aus polymeren monovinylaromatischen Kohlenwasserstoffen | |
| DE1244161B (de) | Stabilisierung von Vinylacetat bei der Destillation | |
| DE1282920B (de) | Verfahren zum Stabilisieren von Polymerisaten aus Olefinen |