DE1569123A1 - Feuerhemmende Masse - Google Patents
Feuerhemmende MasseInfo
- Publication number
- DE1569123A1 DE1569123A1 DE19631569123 DE1569123A DE1569123A1 DE 1569123 A1 DE1569123 A1 DE 1569123A1 DE 19631569123 DE19631569123 DE 19631569123 DE 1569123 A DE1569123 A DE 1569123A DE 1569123 A1 DE1569123 A1 DE 1569123A1
- Authority
- DE
- Germany
- Prior art keywords
- chlorine
- parts
- thermally unstable
- amount
- antimony
- 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
- 239000003063 flame retardant Substances 0.000 title description 21
- 239000000463 material Substances 0.000 claims description 83
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 43
- 239000000460 chlorine Substances 0.000 claims description 42
- 229910052801 chlorine Inorganic materials 0.000 claims description 42
- 229920003023 plastic Polymers 0.000 claims description 38
- 239000004033 plastic Substances 0.000 claims description 38
- 150000001463 antimony compounds Chemical class 0.000 claims description 23
- 239000002245 particle Substances 0.000 claims description 20
- 230000009970 fire resistant effect Effects 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 13
- 229910052787 antimony Inorganic materials 0.000 claims description 12
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 claims description 12
- 229920000642 polymer Polymers 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 11
- 239000012188 paraffin wax Substances 0.000 claims description 10
- 150000001875 compounds Chemical class 0.000 claims description 9
- 229920000620 organic polymer Polymers 0.000 claims description 9
- LIYKJALVRPGQTR-UHFFFAOYSA-M oxostibanylium;chloride Chemical compound [Cl-].[Sb+]=O LIYKJALVRPGQTR-UHFFFAOYSA-M 0.000 claims description 8
- 229920001225 polyester resin Polymers 0.000 claims description 4
- 239000004645 polyester resin Substances 0.000 claims description 4
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 claims description 3
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 101100118976 Mus musculus Clint1 gene Proteins 0.000 claims 1
- FAPDDOBMIUGHIN-UHFFFAOYSA-K antimony trichloride Chemical compound Cl[Sb](Cl)Cl FAPDDOBMIUGHIN-UHFFFAOYSA-K 0.000 claims 1
- 239000003575 carbonaceous material Substances 0.000 claims 1
- 238000010304 firing Methods 0.000 claims 1
- 239000002991 molded plastic Substances 0.000 claims 1
- -1 etc. Polymers 0.000 description 13
- 229920000915 polyvinyl chloride Polymers 0.000 description 11
- 239000004800 polyvinyl chloride Substances 0.000 description 11
- 238000012360 testing method Methods 0.000 description 9
- 239000004698 Polyethylene Substances 0.000 description 6
- 239000004793 Polystyrene Substances 0.000 description 6
- 239000004700 high-density polyethylene Substances 0.000 description 6
- 229920000573 polyethylene Polymers 0.000 description 6
- 229920002223 polystyrene Polymers 0.000 description 6
- 239000000523 sample Substances 0.000 description 6
- 229920001903 high density polyethylene Polymers 0.000 description 5
- 229910000410 antimony oxide Inorganic materials 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000011888 foil Substances 0.000 description 4
- 229920001684 low density polyethylene Polymers 0.000 description 4
- 239000004702 low-density polyethylene Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 4
- 239000004743 Polypropylene Substances 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- RCJVRSBWZCNNQT-UHFFFAOYSA-N dichloridooxygen Chemical compound ClOCl RCJVRSBWZCNNQT-UHFFFAOYSA-N 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 229920001155 polypropylene Polymers 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 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 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- 238000004061 bleaching Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 239000002861 polymer material Substances 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- 239000005033 polyvinylidene chloride Substances 0.000 description 2
- 239000013074 reference sample Substances 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- PPBRFJLRPRQPEC-UHFFFAOYSA-N 1,3,4-trichloro-5-(2,3,5-trichlorophenyl)-2-(3,4,5-trichlorophenyl)benzene Chemical compound ClC1=CC(Cl)=C(Cl)C(C=2C(=C(Cl)C(=C(Cl)C=2)C=2C=C(Cl)C(Cl)=C(Cl)C=2)Cl)=C1 PPBRFJLRPRQPEC-UHFFFAOYSA-N 0.000 description 1
- 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
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 101100002081 Dickeya chrysanthemi arbB gene Proteins 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 241000272184 Falconiformes Species 0.000 description 1
- 229920006385 Geon Polymers 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229910000806 Latten Inorganic materials 0.000 description 1
- KWORKYDIARWARF-UHFFFAOYSA-N N-(4-chloro-2-methylphenyl)-4-[(4-chloro-2-methylphenyl)diazenyl]-3-hydroxynaphthalene-2-carboxamide Chemical compound Cc1cc(Cl)ccc1NC(=O)c1cc2ccccc2c(N=Nc2ccc(Cl)cc2C)c1O KWORKYDIARWARF-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 102100024237 Stathmin Human genes 0.000 description 1
- 108050003387 Stathmin Proteins 0.000 description 1
- 229920006266 Vinyl film Polymers 0.000 description 1
- XLGNVNJCHMVSGV-UHFFFAOYSA-N [Sb].[Si]=O Chemical compound [Sb].[Si]=O XLGNVNJCHMVSGV-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 229940074323 antara Drugs 0.000 description 1
- 229940058905 antimony compound for treatment of leishmaniasis and trypanosomiasis Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- DGQLVPJVXFOQEV-JNVSTXMASA-N carminic acid Chemical compound OC1=C2C(=O)C=3C(C)=C(C(O)=O)C(O)=CC=3C(=O)C2=C(O)C(O)=C1[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O DGQLVPJVXFOQEV-JNVSTXMASA-N 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 238000005253 cladding Methods 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000013068 control sample Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- YMTINGFKWWXKFG-UHFFFAOYSA-N fenofibrate Chemical compound C1=CC(OC(C)(C)C(=O)OC(C)C)=CC=C1C(=O)C1=CC=C(Cl)C=C1 YMTINGFKWWXKFG-UHFFFAOYSA-N 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000012785 packaging film Substances 0.000 description 1
- 229920006280 packaging film Polymers 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 239000002952 polymeric resin Substances 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 239000001044 red dye Substances 0.000 description 1
- 230000003763 resistance to breakage Effects 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 238000003856 thermoforming Methods 0.000 description 1
- NSBGJRFJIJFMGW-UHFFFAOYSA-N trisodium;stiborate Chemical compound [Na+].[Na+].[Na+].[O-][Sb]([O-])([O-])=O NSBGJRFJIJFMGW-UHFFFAOYSA-N 0.000 description 1
- MECHNRXZTMCUDQ-RKHKHRCZSA-N vitamin D2 Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)/C=C/[C@H](C)C(C)C)=C\C=C1\C[C@@H](O)CCC1=C MECHNRXZTMCUDQ-RKHKHRCZSA-N 0.000 description 1
- 235000001892 vitamin D2 Nutrition 0.000 description 1
- 239000011653 vitamin D2 Substances 0.000 description 1
- 239000011800 void material 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
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/16—Halogen-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
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)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US16910262A | 1962-01-26 | 1962-01-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1569123A1 true DE1569123A1 (de) | 1969-07-24 |
Family
ID=22614272
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19631569123 Pending DE1569123A1 (de) | 1962-01-26 | 1963-01-25 | Feuerhemmende Masse |
Country Status (4)
| Country | Link |
|---|---|
| BE (1) | BE627622A (en, 2012) |
| DE (1) | DE1569123A1 (en, 2012) |
| GB (1) | GB1008994A (en, 2012) |
| NL (1) | NL288263A (en, 2012) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3310880A1 (de) * | 1983-03-25 | 1984-10-04 | Minnesota Mining And Manufacturing Co., Saint Paul, Minn. | Vergossene kabelverbindung |
| DE3432158A1 (de) * | 1984-08-31 | 1986-03-13 | Minnesota Mining And Manufacturing Co., Saint Paul, Minn. | Gegen feuer widerstandsfaehige vergossene kabelverbindung |
| US4822953A (en) * | 1985-09-19 | 1989-04-18 | Minnesota Mining And Manufacturing Company | Fire-protected electrical cable connection |
| US5091608A (en) * | 1988-07-27 | 1992-02-25 | Minnesota Mining And Manufacturing Company | Flame retardant splicing system |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1301505B (de) * | 1964-10-01 | 1969-08-21 | Polymer Corp | Verfahren zur Herstellung von flammhemmendem Latexschaumgummi |
| DE3032192C2 (de) * | 1980-08-27 | 1982-10-07 | Chemische Fabrik Kalk GmbH, 5000 Köln | Brandgeschützte thermoplastische Kunststoffe, elastomere Kunststoffe, duromere Kunststoffe und Kautschuk |
-
0
- BE BE627622D patent/BE627622A/xx unknown
- NL NL288263D patent/NL288263A/xx unknown
-
1963
- 1963-01-25 DE DE19631569123 patent/DE1569123A1/de active Pending
- 1963-01-25 GB GB326463A patent/GB1008994A/en not_active Expired
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3310880A1 (de) * | 1983-03-25 | 1984-10-04 | Minnesota Mining And Manufacturing Co., Saint Paul, Minn. | Vergossene kabelverbindung |
| DE3432158A1 (de) * | 1984-08-31 | 1986-03-13 | Minnesota Mining And Manufacturing Co., Saint Paul, Minn. | Gegen feuer widerstandsfaehige vergossene kabelverbindung |
| US4822953A (en) * | 1985-09-19 | 1989-04-18 | Minnesota Mining And Manufacturing Company | Fire-protected electrical cable connection |
| US5091608A (en) * | 1988-07-27 | 1992-02-25 | Minnesota Mining And Manufacturing Company | Flame retardant splicing system |
Also Published As
| Publication number | Publication date |
|---|---|
| BE627622A (en, 2012) | |
| GB1008994A (en) | 1965-11-03 |
| NL288263A (en, 2012) |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2739429C3 (de) | Schwer entflammbare Formmasse auf der Basis von thermoplastischen Harzen | |
| DE1769823C3 (de) | Farbstabilisierte Polycarbonatmassen | |
| DE2158432A1 (de) | Verstärkte Polyalkylenterephthalatmassen mit verringerter Brennbarkeit | |
| DE2233743A1 (de) | Stabilisiertes polyvinylchlorid und stabilisierungsmischungen hierfuer | |
| DE2546668A1 (de) | Selbstloeschende kunststoffmasse | |
| DE2733695A1 (de) | Stabilisierte feuerhemmende styrolpolymermischungen | |
| DE69110598T2 (de) | Beschichtungen auf Basis thermoplastischer Elastomere, insbesondere Fussbodenbeläge. | |
| DE2736513A1 (de) | Polyvinylchloridpolymer | |
| EP2688981A1 (de) | Flammschutz | |
| DE2263005A1 (de) | Feuerhemmende zubereitungen | |
| DE2154095A1 (de) | Ammoniumpolyphosphat-Phosphoniumbromid-Kombinationen als feuerhemmende Mittel für Propylenpolymere | |
| DE69923230T2 (de) | Polycarbonat-folie mit verbesserter flammhemmungsleistung | |
| EP0025544A1 (de) | Thermoplastische Masse | |
| DE1569123A1 (de) | Feuerhemmende Masse | |
| DE2800923C2 (de) | Flammfeste aromatische Polycarbonate mit guten mechanischen Eigenschaften und guter Schmelzstabilität | |
| DE69010333T2 (de) | Gegen ultraviolettes licht stabile polymerzusammensetzungen. | |
| DE3208842A1 (de) | Formungsgemische | |
| DE2853580A1 (de) | Flammwidrige pvc-mischungen | |
| DE2328535B2 (de) | Flammfeste formmassen auf der basis von acryl-nitril-butadien-styrol- polymerisaten | |
| DE1694494A1 (de) | Flammbestaendige Nylonzusammensetzungen | |
| DE69426549T2 (de) | Polymerische Zusammensetzung aus sehr niedriger Dichte, Polyethylene und ihre Verwendung für Tunnelauskleidungen | |
| DE2112005A1 (de) | Flammverzoegernde Masse und deren Verwendung | |
| DE2007706A1 (de) | Verfahren zur Erzielung von Selbstauslöschungsflamm-Eigenschaften bei schlagfestigkeit smodifiziertem Polyvinylchlorid | |
| DE2437525C2 (de) | Form- und Preßmassen | |
| DE2228952A1 (de) | Entflammungsbestandige Massen |