DE2206020C3 - Flammhemmende Zusammensetzung - Google Patents
Flammhemmende ZusammensetzungInfo
- Publication number
- DE2206020C3 DE2206020C3 DE2206020A DE2206020A DE2206020C3 DE 2206020 C3 DE2206020 C3 DE 2206020C3 DE 2206020 A DE2206020 A DE 2206020A DE 2206020 A DE2206020 A DE 2206020A DE 2206020 C3 DE2206020 C3 DE 2206020C3
- Authority
- DE
- Germany
- Prior art keywords
- fire retardant
- weight
- composition
- adduct
- composition according
- 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 description 111
- 239000003063 flame retardant Substances 0.000 title claims description 77
- 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 description 22
- -1 radical Hydrocarbon Chemical class 0.000 claims description 39
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 claims description 28
- 239000012747 synergistic agent Substances 0.000 claims description 28
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 26
- 125000004432 carbon atom Chemical group C* 0.000 claims description 26
- 239000001301 oxygen Substances 0.000 claims description 26
- 229910052760 oxygen Inorganic materials 0.000 claims description 26
- 229920000642 polymer Polymers 0.000 claims description 24
- 239000004743 Polypropylene Substances 0.000 claims description 23
- 229920001155 polypropylene Polymers 0.000 claims description 23
- 150000001875 compounds Chemical class 0.000 claims description 19
- 125000001931 aliphatic group Chemical group 0.000 claims description 18
- 238000005698 Diels-Alder reaction Methods 0.000 claims description 17
- 239000000460 chlorine Substances 0.000 claims description 12
- 239000000463 material Substances 0.000 claims description 11
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 10
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 claims description 10
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims description 10
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 9
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 9
- 229910052794 bromium Chemical group 0.000 claims description 9
- ZSWFCLXCOIISFI-UHFFFAOYSA-N endo-cyclopentadiene Natural products C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 claims description 9
- 239000011368 organic material Substances 0.000 claims description 9
- 229910052736 halogen Inorganic materials 0.000 claims description 8
- 150000002367 halogens Chemical group 0.000 claims description 8
- 229930195733 hydrocarbon Natural products 0.000 claims description 8
- 125000001246 bromo group Chemical group Br* 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 238000006253 efflorescence Methods 0.000 claims description 7
- 206010037844 rash Diseases 0.000 claims description 7
- 239000011347 resin Substances 0.000 claims description 7
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- 239000004215 Carbon black (E152) Substances 0.000 claims description 6
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 claims description 6
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 5
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 claims description 5
- 150000001993 dienes Chemical class 0.000 claims description 5
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 claims description 4
- 239000001257 hydrogen Chemical group 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 3
- 150000002430 hydrocarbons Chemical group 0.000 claims description 3
- YLUZWKKWWSCRSR-UHFFFAOYSA-N 3,9-bis(8-methylnonoxy)-2,4,8,10-tetraoxa-3,9-diphosphaspiro[5.5]undecane Chemical compound C1OP(OCCCCCCCC(C)C)OCC21COP(OCCCCCCCC(C)C)OC2 YLUZWKKWWSCRSR-UHFFFAOYSA-N 0.000 claims description 2
- PZRWFKGUFWPFID-UHFFFAOYSA-N 3,9-dioctadecoxy-2,4,8,10-tetraoxa-3,9-diphosphaspiro[5.5]undecane Chemical group C1OP(OCCCCCCCCCCCCCCCCCC)OCC21COP(OCCCCCCCCCCCCCCCCCC)OC2 PZRWFKGUFWPFID-UHFFFAOYSA-N 0.000 claims description 2
- 229930185605 Bisphenol Natural products 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 229910052787 antimony Inorganic materials 0.000 claims description 2
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 claims description 2
- 229910052785 arsenic Inorganic materials 0.000 claims description 2
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 claims description 2
- 229910052797 bismuth Inorganic materials 0.000 claims description 2
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 claims description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims description 2
- 238000009835 boiling Methods 0.000 claims description 2
- 229920000098 polyolefin Polymers 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- 229910052717 sulfur Chemical group 0.000 claims description 2
- 239000011593 sulfur Chemical group 0.000 claims description 2
- 229920001169 thermoplastic Polymers 0.000 claims description 2
- GXURZKWLMYOCDX-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol;dihydroxyphosphanyl dihydrogen phosphite Chemical compound OP(O)OP(O)O.OCC(CO)(CO)CO GXURZKWLMYOCDX-UHFFFAOYSA-N 0.000 claims 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 1
- 125000002837 carbocyclic group Chemical group 0.000 claims 1
- 229920001038 ethylene copolymer Polymers 0.000 claims 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 claims 1
- 229940117969 neopentyl glycol Drugs 0.000 claims 1
- 230000009965 odorless effect Effects 0.000 claims 1
- 229910052698 phosphorus Inorganic materials 0.000 claims 1
- 239000011574 phosphorus Substances 0.000 claims 1
- 239000004416 thermosoftening plastic Substances 0.000 claims 1
- VUNCWTMEJYMOOR-UHFFFAOYSA-N hexachlorocyclopentadiene Chemical compound ClC1=C(Cl)C(Cl)(Cl)C(Cl)=C1Cl VUNCWTMEJYMOOR-UHFFFAOYSA-N 0.000 description 16
- 239000002904 solvent Substances 0.000 description 16
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 15
- 239000003112 inhibitor Substances 0.000 description 15
- 229920000877 Melamine resin Polymers 0.000 description 14
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 12
- 238000000034 method Methods 0.000 description 11
- 239000000047 product Substances 0.000 description 10
- 238000012360 testing method Methods 0.000 description 10
- RRKODOZNUZCUBN-CCAGOZQPSA-N (1z,3z)-cycloocta-1,3-diene Chemical compound C1CC\C=C/C=C\C1 RRKODOZNUZCUBN-CCAGOZQPSA-N 0.000 description 9
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 9
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 9
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical group NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 9
- 239000000243 solution Substances 0.000 description 8
- 239000000654 additive Substances 0.000 description 7
- 150000003839 salts Chemical class 0.000 description 7
- 150000004671 saturated fatty acids Chemical class 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 238000000354 decomposition reaction Methods 0.000 description 5
- 238000002347 injection Methods 0.000 description 5
- 239000007924 injection Substances 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- 150000002736 metal compounds Chemical class 0.000 description 5
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 5
- 239000007858 starting material Substances 0.000 description 5
- 150000003918 triazines Chemical class 0.000 description 5
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 239000004698 Polyethylene Substances 0.000 description 4
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 4
- 230000031709 bromination Effects 0.000 description 4
- 238000005893 bromination reaction Methods 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 229920000573 polyethylene Polymers 0.000 description 4
- 235000003441 saturated fatty acids Nutrition 0.000 description 4
- JSZOAYXJRCEYSX-UHFFFAOYSA-N 1-nitropropane Chemical compound CCC[N+]([O-])=O JSZOAYXJRCEYSX-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
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- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 239000005062 Polybutadiene Substances 0.000 description 3
- 235000021355 Stearic acid Nutrition 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- LRHPLDYGYMQRHN-UHFFFAOYSA-N butyl alcohol Substances CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
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- 230000000694 effects Effects 0.000 description 3
- 238000000605 extraction Methods 0.000 description 3
- 125000000623 heterocyclic group Chemical group 0.000 description 3
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- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical class [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 3
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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
- C08K5/02—Halogenated 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Paper (AREA)
- Fireproofing Substances (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11508171A | 1971-02-12 | 1971-02-12 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| DE2206020A1 DE2206020A1 (de) | 1972-08-24 |
| DE2206020B2 DE2206020B2 (de) | 1974-03-14 |
| DE2206020C3 true DE2206020C3 (de) | 1974-10-31 |
Family
ID=22359213
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2206020A Expired DE2206020C3 (de) | 1971-02-12 | 1972-02-09 | Flammhemmende Zusammensetzung |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US4127559A (OSRAM) |
| JP (1) | JPS5123840B1 (OSRAM) |
| BE (1) | BE779264A (OSRAM) |
| CA (1) | CA1054284A (OSRAM) |
| DE (1) | DE2206020C3 (OSRAM) |
| FR (1) | FR2125427B1 (OSRAM) |
| GB (1) | GB1377282A (OSRAM) |
| IT (1) | IT948997B (OSRAM) |
| NL (1) | NL144315B (OSRAM) |
| ZA (1) | ZA718662B (OSRAM) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4098761A (en) | 1974-03-04 | 1978-07-04 | Hooker Chemicals & Plastics Corp. | Halogen containing fire retardant additive with improved heat stability |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2300114C3 (de) * | 1973-01-03 | 1983-03-10 | Basf Ag, 6700 Ludwigshafen | Selbstverlöschende Formmassen aus Styrolpolymerisaten |
| US4289687A (en) * | 1979-01-22 | 1981-09-15 | Japan Atomic Energy Research Institute | Fire retardant resin molded product and preparation process of the same |
| JPS6025063B2 (ja) * | 1980-03-03 | 1985-06-15 | 日本原子力研究所 | 高分子物質の耐放射線性難燃化処理方法 |
| US4820770A (en) * | 1988-01-25 | 1989-04-11 | Ethyl Corporation | Polyamide composition |
| US4857597A (en) * | 1988-02-01 | 1989-08-15 | Ethyl Corporation | Thermoplastic formulations |
| US5104604A (en) * | 1989-10-05 | 1992-04-14 | Dexter Electronic Materials Div. Of Dexter Corp. | Flame retardant epoxy molding compound, method and encapsulated device method of encapsulating a semiconductor device with a flame retardant epoxy molding compound |
| US5476716A (en) * | 1988-10-17 | 1995-12-19 | The Dexter Corporation | Flame retardant epoxy molding compound, method and encapsulated device |
| US5084213A (en) * | 1990-03-05 | 1992-01-28 | Ethyl Corporation | Mixed halogenation of cyclododecatriene |
| US5439965A (en) * | 1993-09-16 | 1995-08-08 | Quantum Chemical Corporation | Abrasion resistant crosslinkable insulation compositions |
| CN109705507B (zh) * | 2018-11-30 | 2020-11-17 | 金发科技股份有限公司 | 一种阻燃hips材料及其制备方法 |
| CN109705506B (zh) * | 2018-11-30 | 2020-11-17 | 金发科技股份有限公司 | 一种阻燃hips材料及其制备方法 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2741641A (en) * | 1950-06-13 | 1956-04-10 | Velsicol Chemical Corp | Manufacture of chlorinated compounds |
| US3050567A (en) * | 1954-03-29 | 1962-08-21 | Universal Oil Prod Co | Polycyclic compounds containing nuclearly substituted halogens |
| US3025329A (en) * | 1959-03-02 | 1962-03-13 | Exxon Research Engineering Co | Halogenated derivatives of cyclododecatriene |
| NL289359A (OSRAM) * | 1962-02-22 | |||
| GB1090598A (en) * | 1964-08-17 | 1967-11-08 | Hooker Chemical Corp | Polymers and coatings rendered flame retardant by the addition of halogenated cyclopentadiene diels-alder adducts |
| US3365505A (en) * | 1965-10-22 | 1968-01-23 | Phillips Petroleum Co | Novel halogenated compounds and methods for the preparation thereof |
| US3410916A (en) * | 1966-05-31 | 1968-11-12 | Olin Mathieson | 5, 6, 7, 8, 11, 11, 12, 12-octachloro-2, 3, 3a, 4, 4a, 5, 8, 8a, 9, 9a-decahydro-2, 3:4, 9:5, 8-trimethano-1h-cyclopenta(3a:9a) naphthalene |
| US3396201A (en) * | 1966-11-30 | 1968-08-06 | Hooker Chemical Corp | Adducts of hexahalocyclopentadiene with alkadienes |
| US3697607A (en) * | 1970-01-02 | 1972-10-10 | Phillips Petroleum Co | Brominated adducts of acyclic trienes |
-
1971
- 1971-12-28 ZA ZA718662A patent/ZA718662B/xx unknown
-
1972
- 1972-01-11 CA CA132,189A patent/CA1054284A/en not_active Expired
- 1972-02-01 GB GB472372A patent/GB1377282A/en not_active Expired
- 1972-02-02 IT IT67309/72A patent/IT948997B/it active
- 1972-02-08 NL NL727201618A patent/NL144315B/xx not_active IP Right Cessation
- 1972-02-09 DE DE2206020A patent/DE2206020C3/de not_active Expired
- 1972-02-10 JP JP47014077A patent/JPS5123840B1/ja active Pending
- 1972-02-11 FR FR7204747A patent/FR2125427B1/fr not_active Expired
- 1972-02-11 BE BE779264A patent/BE779264A/xx unknown
- 1972-08-18 US US05/281,692 patent/US4127559A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4098761A (en) | 1974-03-04 | 1978-07-04 | Hooker Chemicals & Plastics Corp. | Halogen containing fire retardant additive with improved heat stability |
Also Published As
| Publication number | Publication date |
|---|---|
| ZA718662B (en) | 1972-09-27 |
| FR2125427B1 (OSRAM) | 1977-04-01 |
| DE2206020B2 (de) | 1974-03-14 |
| BE779264A (fr) | 1972-08-11 |
| DE2206020A1 (de) | 1972-08-24 |
| NL144315B (nl) | 1974-12-16 |
| NL7201618A (OSRAM) | 1972-08-15 |
| CA1054284A (en) | 1979-05-08 |
| IT948997B (it) | 1973-06-11 |
| US4127559A (en) | 1978-11-28 |
| FR2125427A1 (OSRAM) | 1972-09-29 |
| GB1377282A (en) | 1974-12-11 |
| JPS5123840B1 (OSRAM) | 1976-07-20 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C3 | Grant after two publication steps (3rd publication) | ||
| E77 | Valid patent as to the heymanns-index 1977 | ||
| 8327 | Change in the person/name/address of the patent owner |
Owner name: ETHYL CORP., 23219 RICHMOND, VA., US |
|
| 8328 | Change in the person/name/address of the agent |
Free format text: BOEHMERT, A., DIPL.-ING. HOORMANN, W., DIPL.-ING. DR.-ING. GODDAR, H., DIPL.-PHYS. DR.RER.NAT., PAT.-ANW. STAHLBERG, W. KUNTZE, W., RECHTSANW., 2800 BREMEN |
|
| 8339 | Ceased/non-payment of the annual fee |