DE2046795B2 - Selbstverlöschende Formmassen auf der Basis von Acrylnitril-Butadien-Styrol-Polymerisaten - Google Patents
Selbstverlöschende Formmassen auf der Basis von Acrylnitril-Butadien-Styrol-PolymerisatenInfo
- Publication number
- DE2046795B2 DE2046795B2 DE2046795A DE2046795A DE2046795B2 DE 2046795 B2 DE2046795 B2 DE 2046795B2 DE 2046795 A DE2046795 A DE 2046795A DE 2046795 A DE2046795 A DE 2046795A DE 2046795 B2 DE2046795 B2 DE 2046795B2
- Authority
- DE
- Germany
- Prior art keywords
- self
- acrylonitrile
- butadiene
- bromine
- molding compounds
- 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.)
- Withdrawn
Links
- 229920000642 polymer Polymers 0.000 title claims description 20
- 150000001875 compounds Chemical class 0.000 title claims description 9
- 238000000465 moulding Methods 0.000 title claims description 8
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 title description 16
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 title description 16
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 title description 16
- -1 aromatic bromine compound Chemical class 0.000 description 16
- 229910052794 bromium Inorganic materials 0.000 description 13
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 12
- 239000000460 chlorine Substances 0.000 description 12
- 229910052801 chlorine Inorganic materials 0.000 description 12
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 10
- 239000003063 flame retardant Substances 0.000 description 10
- 239000000203 mixture Substances 0.000 description 9
- 229910052739 hydrogen Inorganic materials 0.000 description 8
- 239000001257 hydrogen Substances 0.000 description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 6
- 125000001246 bromo group Chemical group Br* 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- 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 description 5
- 229920003023 plastic Polymers 0.000 description 5
- 239000004033 plastic Substances 0.000 description 5
- 125000003342 alkenyl group Chemical group 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- 125000001188 haloalkyl group Chemical group 0.000 description 4
- VUNCWTMEJYMOOR-UHFFFAOYSA-N hexachlorocyclopentadiene Chemical class ClC1=C(Cl)C(Cl)(Cl)C(Cl)=C1Cl VUNCWTMEJYMOOR-UHFFFAOYSA-N 0.000 description 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
- 150000001805 chlorine compounds Chemical class 0.000 description 3
- 150000005526 organic bromine compounds Chemical class 0.000 description 3
- 239000004800 polyvinyl chloride Substances 0.000 description 3
- 229920000915 polyvinyl chloride Polymers 0.000 description 3
- NDRKXFLZSRHAJE-UHFFFAOYSA-N 1,2,3,4,5-pentabromo-6-(2,3,4-tribromophenyl)benzene Chemical group BrC1=C(Br)C(Br)=CC=C1C1=C(Br)C(Br)=C(Br)C(Br)=C1Br NDRKXFLZSRHAJE-UHFFFAOYSA-N 0.000 description 2
- 239000004801 Chlorinated PVC Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 150000001463 antimony compounds Chemical class 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 229920000457 chlorinated polyvinyl chloride Polymers 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- LIYKJALVRPGQTR-UHFFFAOYSA-M oxostibanylium;chloride Chemical compound [Cl-].[Sb+]=O LIYKJALVRPGQTR-UHFFFAOYSA-M 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- VCNJVIWFSMCZPE-UHFFFAOYSA-N 1,2,3,4,5-pentabromo-6-prop-2-enoxybenzene Chemical compound BrC1=C(Br)C(Br)=C(OCC=C)C(Br)=C1Br VCNJVIWFSMCZPE-UHFFFAOYSA-N 0.000 description 1
- ORYGKUIDIMIRNN-UHFFFAOYSA-N 1,2,3,4-tetrabromo-5-(2,3,4,5-tetrabromophenoxy)benzene Chemical compound BrC1=C(Br)C(Br)=CC(OC=2C(=C(Br)C(Br)=C(Br)C=2)Br)=C1Br ORYGKUIDIMIRNN-UHFFFAOYSA-N 0.000 description 1
- XTOGZIGVBPDWQI-UHFFFAOYSA-N 1,3,5-tribromo-2-[1,2-dibromo-3-[2,3-dibromo-3-(2,4,6-tribromophenyl)propoxy]propyl]benzene Chemical compound BrC=1C=C(Br)C=C(Br)C=1C(Br)C(Br)COCC(Br)C(Br)C1=C(Br)C=C(Br)C=C1Br XTOGZIGVBPDWQI-UHFFFAOYSA-N 0.000 description 1
- LXIZRZRTWSDLKK-UHFFFAOYSA-N 1,3-dibromo-5-[2-[3,5-dibromo-4-(2,3-dibromopropoxy)phenyl]propan-2-yl]-2-(2,3-dibromopropoxy)benzene Chemical compound C=1C(Br)=C(OCC(Br)CBr)C(Br)=CC=1C(C)(C)C1=CC(Br)=C(OCC(Br)CBr)C(Br)=C1 LXIZRZRTWSDLKK-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N dimethylmethane Natural products CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000003106 haloaryl group Chemical group 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 150000004045 organic chlorine compounds Chemical class 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000011265 semifinished product Substances 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
- C08K13/00—Use of mixtures of ingredients not covered by one single of the preceding main groups, each of these compounds being essential
- C08K13/02—Organic and inorganic ingredients
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L55/00—Compositions of homopolymers or copolymers, obtained by polymerisation reactions only involving carbon-to-carbon unsaturated bonds, not provided for in groups C08L23/00 - C08L53/00
- C08L55/02—ABS [Acrylonitrile-Butadiene-Styrene] polymers
-
- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K3/2279—Oxides; Hydroxides of metals of antimony
-
- 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
- C08K5/03—Halogenated hydrocarbons aromatic, e.g. C6H5-CH2-Cl
-
- 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
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/26—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers modified by chemical after-treatment
- C08L23/28—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers modified by chemical after-treatment by reaction with halogens or halogen-containing compounds
- C08L23/286—Chlorinated polyethene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—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 a halogen; Compositions of derivatives of such polymers
- C08L27/22—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 a halogen; Compositions of derivatives of such polymers modified by chemical after-treatment
- C08L27/24—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 a halogen; Compositions of derivatives of such polymers modified by chemical after-treatment halogenated
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)
- Fireproofing Substances (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Priority Applications (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2046795A DE2046795B2 (de) | 1970-09-23 | 1970-09-23 | Selbstverlöschende Formmassen auf der Basis von Acrylnitril-Butadien-Styrol-Polymerisaten |
| FR7129421A FR2105858A5 (enExample) | 1970-09-23 | 1971-08-11 | |
| BE771653A BE771653A (fr) | 1970-09-23 | 1971-08-23 | Masses a mouler autoextinctrices a base de polymeres d'acrylonitrile-butadiene-styrene |
| NL7111993.A NL166045C (nl) | 1970-09-23 | 1971-08-31 | Werkwijze ter bereiding van zelfdovende mengsels op basis van thermoplastische acrylonitrile-butadieen- -styreen-polymeren. |
| GB4168671A GB1345211A (en) | 1970-09-23 | 1971-09-07 | Self-extinguishing moulding compositions based on acrylontrile- butadiene-styrene polymers |
| IT12925/71A IT943556B (it) | 1970-09-23 | 1971-09-16 | Prodotti autoestinguenti a base di polimeri di acrilonitrile butadie ne stirolo |
| US00182542A US3830766A (en) | 1970-09-23 | 1971-09-21 | Self-extinguishing moulding composition |
| JP7390871A JPS565784B1 (enExample) | 1970-09-23 | 1971-09-23 | |
| US05/485,558 US3962164A (en) | 1970-09-23 | 1974-07-03 | Self-extinguishing acrylonitrile-butadiene-styrene moulding composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2046795A DE2046795B2 (de) | 1970-09-23 | 1970-09-23 | Selbstverlöschende Formmassen auf der Basis von Acrylnitril-Butadien-Styrol-Polymerisaten |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2046795A1 DE2046795A1 (de) | 1972-03-30 |
| DE2046795B2 true DE2046795B2 (de) | 1975-05-07 |
Family
ID=5783126
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2046795A Withdrawn DE2046795B2 (de) | 1970-09-23 | 1970-09-23 | Selbstverlöschende Formmassen auf der Basis von Acrylnitril-Butadien-Styrol-Polymerisaten |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US3830766A (enExample) |
| JP (1) | JPS565784B1 (enExample) |
| BE (1) | BE771653A (enExample) |
| DE (1) | DE2046795B2 (enExample) |
| FR (1) | FR2105858A5 (enExample) |
| GB (1) | GB1345211A (enExample) |
| IT (1) | IT943556B (enExample) |
| NL (1) | NL166045C (enExample) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2408681A1 (de) * | 1973-02-22 | 1974-09-05 | Montedison Spa | Verfahren zur herstellung von formkoerpern |
| US4200702A (en) | 1977-06-18 | 1980-04-29 | Basf Aktiengesellschaft | Self-extinguishing thermoplastic molding compositions |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3883481A (en) * | 1966-10-28 | 1975-05-13 | Huels Chemische Werke Ag | Fire-retardant polyolefin compositions |
| US3962164A (en) * | 1970-09-23 | 1976-06-08 | Chemische Fabrik Kalk Gmbh | Self-extinguishing acrylonitrile-butadiene-styrene moulding composition |
| US3989531A (en) * | 1971-08-05 | 1976-11-02 | General Electric Company | Fire-retardant polymeric compositions containing brominated biphenols |
| US3965214A (en) * | 1971-12-17 | 1976-06-22 | Michigan Chemical Corporation | Flame retardant ABS polymer compositions |
| US3957722A (en) * | 1973-07-05 | 1976-05-18 | The Firestone Tire & Rubber Company | Flame-resistant polybutadiene resin |
| US3953396A (en) * | 1973-12-28 | 1976-04-27 | General Electric Company | Flame retardant polycarbonate composition |
| US4032506A (en) * | 1973-12-28 | 1977-06-28 | General Electric Company | Flame retardant polycarbonate composition |
| US4033916A (en) * | 1974-10-17 | 1977-07-05 | Uniroyal Inc. | Ternary flame-retarded compositions including iron oxide |
| US4000114A (en) * | 1975-02-24 | 1976-12-28 | Hooker Chemicals & Plastics Corporation | Fire retardant polymer compositions with improved physical properties |
| US4144225A (en) * | 1975-08-18 | 1979-03-13 | Kanebo, Ltd. | Novel aromatic diamine compounds and flame-resistant polyamide compositions containing said compounds |
| US4138447A (en) * | 1977-06-20 | 1979-02-06 | Monsanto Company | Nitrogenous polymer compositions |
| US4230821A (en) * | 1979-02-26 | 1980-10-28 | Labofina, S.A. | Fire-retardant polystyrenic compositions |
| US4623583A (en) * | 1979-04-18 | 1986-11-18 | White Chemical Corporation | Flame retardant textile fabrics |
| US4600606A (en) * | 1979-04-18 | 1986-07-15 | White Chemical Corporation | Process for rendering non-thermoplastic fibrous materials flame resistant to molten materials by application thereto of a flame resistant composition, and related articles and compositions |
| US4456721A (en) * | 1982-12-02 | 1984-06-26 | Borg-Warner Chemicals, Inc. | Flame-retarded acrylonitrile-butadiene-styrene copolymer compositions comprising bis(beta-pentabromophenoxyethyl) succinate |
| DE3307051A1 (de) * | 1983-03-01 | 1984-09-06 | Basf Ag, 6700 Ludwigshafen | Schwerentflammbare, transparente poly-(arylether-aryl-sulfon)-formmassen, verfahren zu deren herstellung sowie deren verwendung |
| 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 |
| US5112896A (en) * | 1989-06-06 | 1992-05-12 | Ferro Corporation | High-impact polystyrene containing low molecular weight brominated polystyrene |
| US5112897A (en) * | 1989-06-06 | 1992-05-12 | Ferro Corporation | High impact polystyrene containing low molecular weight brominated polystyrene |
| US5112898A (en) * | 1989-06-06 | 1992-05-12 | Ferro Corporation | High impact polystyrene containing low molecular weight brominated polystyrene |
| US20080221239A1 (en) * | 2007-03-07 | 2008-09-11 | Falloon Stephen B | Flame retardant composition for use in styrenics |
| US9481621B2 (en) * | 2013-01-06 | 2016-11-01 | Bromine Compounds Ltd. | Preparation of bromine-containing aromatic compounds and their application as flame retardants |
-
1970
- 1970-09-23 DE DE2046795A patent/DE2046795B2/de not_active Withdrawn
-
1971
- 1971-08-11 FR FR7129421A patent/FR2105858A5/fr not_active Expired
- 1971-08-23 BE BE771653A patent/BE771653A/xx unknown
- 1971-08-31 NL NL7111993.A patent/NL166045C/xx not_active IP Right Cessation
- 1971-09-07 GB GB4168671A patent/GB1345211A/en not_active Expired
- 1971-09-16 IT IT12925/71A patent/IT943556B/it active
- 1971-09-21 US US00182542A patent/US3830766A/en not_active Expired - Lifetime
- 1971-09-23 JP JP7390871A patent/JPS565784B1/ja active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2408681A1 (de) * | 1973-02-22 | 1974-09-05 | Montedison Spa | Verfahren zur herstellung von formkoerpern |
| US4200702A (en) | 1977-06-18 | 1980-04-29 | Basf Aktiengesellschaft | Self-extinguishing thermoplastic molding compositions |
Also Published As
| Publication number | Publication date |
|---|---|
| GB1345211A (en) | 1974-01-30 |
| NL7111993A (enExample) | 1972-03-27 |
| FR2105858A5 (enExample) | 1972-04-28 |
| DE2046795A1 (de) | 1972-03-30 |
| JPS565784B1 (enExample) | 1981-02-06 |
| US3830766A (en) | 1974-08-20 |
| IT943556B (it) | 1973-04-10 |
| NL166045B (nl) | 1981-01-15 |
| BE771653A (fr) | 1971-12-31 |
| NL166045C (nl) | 1981-06-15 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8230 | Patent withdrawn |