DE1255302C2 - Thermoplastische Formmassen zur Herstellung selbstverloeschender Formkoerper - Google Patents
Thermoplastische Formmassen zur Herstellung selbstverloeschender FormkoerperInfo
- Publication number
- DE1255302C2 DE1255302C2 DE1965B0082751 DEB0082751A DE1255302C2 DE 1255302 C2 DE1255302 C2 DE 1255302C2 DE 1965B0082751 DE1965B0082751 DE 1965B0082751 DE B0082751 A DEB0082751 A DE B0082751A DE 1255302 C2 DE1255302 C2 DE 1255302C2
- Authority
- DE
- Germany
- Prior art keywords
- polymers
- compounds
- parts
- flame
- self
- 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
- 150000001875 compounds Chemical class 0.000 title claims description 24
- 238000000465 moulding Methods 0.000 title claims description 18
- 238000009757 thermoplastic moulding Methods 0.000 title claims description 4
- 238000004519 manufacturing process Methods 0.000 title description 5
- 229920000642 polymer Polymers 0.000 claims description 48
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 38
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 10
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 8
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 8
- 229910052794 bromium Inorganic materials 0.000 claims description 8
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims description 6
- 238000006116 polymerization reaction Methods 0.000 claims description 4
- 230000031709 bromination Effects 0.000 claims description 3
- 238000005893 bromination reaction Methods 0.000 claims description 3
- 229920003052 natural elastomer Polymers 0.000 claims description 3
- 229920001194 natural rubber Polymers 0.000 claims description 3
- 229920003051 synthetic elastomer Polymers 0.000 claims description 3
- 239000005061 synthetic rubber Substances 0.000 claims description 3
- 239000000203 mixture Substances 0.000 description 23
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
- 239000003063 flame retardant Substances 0.000 description 11
- 239000000126 substance Substances 0.000 description 11
- DEIGXXQKDWULML-UHFFFAOYSA-N 1,2,5,6,9,10-hexabromocyclododecane Chemical compound BrC1CCC(Br)C(Br)CCC(Br)C(Br)CCC1Br DEIGXXQKDWULML-UHFFFAOYSA-N 0.000 description 9
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 9
- 150000005526 organic bromine compounds Chemical class 0.000 description 9
- 125000001424 substituent group Chemical group 0.000 description 8
- SPPWGCYEYAMHDT-UHFFFAOYSA-N 1,4-di(propan-2-yl)benzene Chemical compound CC(C)C1=CC=C(C(C)C)C=C1 SPPWGCYEYAMHDT-UHFFFAOYSA-N 0.000 description 7
- 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 7
- 239000004793 Polystyrene Substances 0.000 description 7
- 229910052736 halogen Inorganic materials 0.000 description 7
- 150000002367 halogens Chemical class 0.000 description 7
- 229920002223 polystyrene Polymers 0.000 description 7
- 230000002195 synergetic effect Effects 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 239000006260 foam Substances 0.000 description 6
- 150000002978 peroxides Chemical class 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 4
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000004604 Blowing Agent Substances 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- UNEATYXSUBPPKP-UHFFFAOYSA-N 1,3-Diisopropylbenzene Chemical compound CC(C)C1=CC=CC(C(C)C)=C1 UNEATYXSUBPPKP-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 230000008033 biological extinction Effects 0.000 description 2
- -1 bromine compound Chemical class 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 150000001451 organic peroxides Chemical class 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 230000000379 polymerizing effect Effects 0.000 description 2
- 239000003380 propellant Substances 0.000 description 2
- ROXLYQQDLJJEBE-UHFFFAOYSA-N 1,2,4,5-tetra(propan-2-yl)benzene Chemical compound CC(C)C1=CC(C(C)C)=C(C(C)C)C=C1C(C)C ROXLYQQDLJJEBE-UHFFFAOYSA-N 0.000 description 1
- BMVSGYZZGVEXTB-UHFFFAOYSA-N 1,4-di(butan-2-yl)benzene Chemical compound CCC(C)C1=CC=C(C(C)CC)C=C1 BMVSGYZZGVEXTB-UHFFFAOYSA-N 0.000 description 1
- KUZWOCIAIWAHEG-UHFFFAOYSA-N 1,4-dichloro-2,5-di(propan-2-yl)benzene Chemical compound CC(C)C1=CC(Cl)=C(C(C)C)C=C1Cl KUZWOCIAIWAHEG-UHFFFAOYSA-N 0.000 description 1
- MBEBPYJMHLBHDJ-UHFFFAOYSA-N 1,4-dimethyl-2,5-di(propan-2-yl)benzene Chemical compound CC(C)C1=CC(C)=C(C(C)C)C=C1C MBEBPYJMHLBHDJ-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- SGDXAVBMPYRDQA-UHFFFAOYSA-N 2-tert-butyl-1,4-di(propan-2-yl)benzene Chemical compound C(C)(C)C1=C(C=C(C=C1)C(C)C)C(C)(C)C SGDXAVBMPYRDQA-UHFFFAOYSA-N 0.000 description 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 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
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 239000004338 Dichlorodifluoromethane Substances 0.000 description 1
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical class OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 1
- 235000000177 Indigofera tinctoria Nutrition 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- NEHMKBQYUWJMIP-NJFSPNSNSA-N chloro(114C)methane Chemical compound [14CH3]Cl NEHMKBQYUWJMIP-NJFSPNSNSA-N 0.000 description 1
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Substances ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 1
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000004794 expanded polystyrene Substances 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 150000002366 halogen compounds Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229940097275 indigo Drugs 0.000 description 1
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920006216 polyvinyl aromatic Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 230000006798 recombination Effects 0.000 description 1
- 238000005215 recombination Methods 0.000 description 1
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 1
- 229940048086 sodium pyrophosphate Drugs 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 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
- C08J9/0095—Mixtures of at least two compounding ingredients belonging to different one-dot groups
-
- 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
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/02—Halogenated hydrocarbons
-
- 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
- C08L25/02—Homopolymers or copolymers of hydrocarbons
- C08L25/04—Homopolymers or copolymers of styrene
-
- 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
- C08L25/02—Homopolymers or copolymers of hydrocarbons
- C08L25/16—Homopolymers or copolymers of alkyl-substituted styrenes
-
- 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
- C08L25/18—Homopolymers or copolymers of aromatic monomers containing elements other than carbon and hydrogen
-
- 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
- C08J2325/04—Homopolymers or copolymers of styrene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L65/00—Compositions of macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain; Compositions of derivatives of such polymers
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S521/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S521/907—Nonurethane flameproofed cellular product
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)
- Processes Of Treating Macromolecular Substances (AREA)
Priority Applications (11)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR1486273D FR1486273A (en, 2012) | 1965-07-09 | ||
DE1965B0082751 DE1255302C2 (de) | 1965-07-09 | 1965-07-09 | Thermoplastische Formmassen zur Herstellung selbstverloeschender Formkoerper |
GB30552/66A GB1146653A (en) | 1965-07-09 | 1966-07-07 | Self-extinguishing thermoplastic compositions |
BR181120/66A BR6681120D0 (pt) | 1965-07-09 | 1966-07-08 | Aperfeicoamento em composicoes moldaveis para o fabrico de corpos moldados auto-extintores de chama |
US563713A US3457204A (en) | 1965-07-09 | 1966-07-08 | Self-extinguishing thermoplastic compositions |
LU51513A LU51513A1 (en, 2012) | 1965-07-09 | 1966-07-08 | |
NL6609646A NL6609646A (en, 2012) | 1965-07-09 | 1966-07-08 | |
IS1573A IS1573A7 (is) | 1965-07-09 | 1966-07-08 | Mótunarefni til framleiðslu á sjálfslökkvandi mótunarhlutum |
SE9413/66A SE312434B (en, 2012) | 1965-07-09 | 1966-07-08 | |
ES0328914A ES328914A1 (es) | 1965-07-09 | 1966-07-09 | Procedimiento para la preparacion de polvos de moldeo autoextintores. |
BE683943D BE683943A (en, 2012) | 1965-07-09 | 1966-07-11 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE1965B0082751 DE1255302C2 (de) | 1965-07-09 | 1965-07-09 | Thermoplastische Formmassen zur Herstellung selbstverloeschender Formkoerper |
Publications (2)
Publication Number | Publication Date |
---|---|
DE1255302B DE1255302B (de) | 1967-11-30 |
DE1255302C2 true DE1255302C2 (de) | 1973-09-20 |
Family
ID=6981639
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE1965B0082751 Expired DE1255302C2 (de) | 1965-07-09 | 1965-07-09 | Thermoplastische Formmassen zur Herstellung selbstverloeschender Formkoerper |
Country Status (11)
Country | Link |
---|---|
US (1) | US3457204A (en, 2012) |
BE (1) | BE683943A (en, 2012) |
BR (1) | BR6681120D0 (en, 2012) |
DE (1) | DE1255302C2 (en, 2012) |
ES (1) | ES328914A1 (en, 2012) |
FR (1) | FR1486273A (en, 2012) |
GB (1) | GB1146653A (en, 2012) |
IS (1) | IS1573A7 (en, 2012) |
LU (1) | LU51513A1 (en, 2012) |
NL (1) | NL6609646A (en, 2012) |
SE (1) | SE312434B (en, 2012) |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2300114C3 (de) * | 1973-01-03 | 1983-03-10 | Basf Ag, 6700 Ludwigshafen | Selbstverlöschende Formmassen aus Styrolpolymerisaten |
DE2338709C2 (de) * | 1973-07-31 | 1975-05-22 | Basf Ag, 6700 Ludwigshafen | Farblose Oligomere des Disopropylbenzols, Verfahren zu ihrer Herstellung und ihre Verwendung |
IT1025744B (it) * | 1973-11-26 | 1978-08-30 | Basf Ag | Masse per formatura termopla stiche autoestinglenti |
FI752642A7 (en, 2012) * | 1974-10-11 | 1976-04-12 | Basf Ag | |
US4178327A (en) * | 1974-12-19 | 1979-12-11 | The Dow Chemical Company | Ar-halo-ar(t-alkyl)styrenes and polymers thereof |
US4122066A (en) * | 1977-06-28 | 1978-10-24 | Borg-Warner Corporation | Flame retardant propylene compositions containing trityl compound synergists |
EP0010586B2 (fr) * | 1978-11-07 | 1987-04-15 | LES CABLES DE LYON Société anonyme dite: | Matériau isolant ignifugé pour câble électrique, et câble électrique obtenu à l'aide de ce matériau |
DE2853992A1 (de) * | 1978-12-14 | 1980-07-03 | Basf Ag | Selbstverloeschende thermoplastische formmassen und formteile aus diesen |
DE2906336C3 (de) * | 1979-02-19 | 1982-01-07 | Chemische Werke Hüls AG, 4370 Marl | Feinteilige selbstverlöschende expandierbare Styrolpolymerisate |
US4359538A (en) * | 1979-03-20 | 1982-11-16 | Labofina, S.A. | Fire-retardant polystyrenic compositions |
DE2929950A1 (de) * | 1979-07-24 | 1981-02-26 | Basf Ag | Di- und/oder oligomerisierung von cyclischen, aliphatischen aethern und verwendung der entstandenen produkte |
US4331780A (en) * | 1980-03-20 | 1982-05-25 | Phillips Petroleum Company | Flame retardant transparent resinous copolymer |
JPH02501663A (ja) * | 1987-10-09 | 1990-06-07 | グレート・レークス・ケミカル・コーポレーション | 難燃性pvc樹脂組成物 |
US4892892A (en) * | 1987-10-09 | 1990-01-09 | Great Lakes Chemical Corporation | Flame retardant polyurethane foam compositions containing polynuclearbrominated alkylbenzene |
US4829118A (en) * | 1987-10-09 | 1989-05-09 | Great Lakes Chemical Corporation | Flame retardant ABS resin compositions |
US5008323A (en) * | 1987-10-09 | 1991-04-16 | Great Lakes Chemical Corporation | Flame retardant PVC resin compositions |
US4831072A (en) * | 1987-10-09 | 1989-05-16 | Great Lakes Chemical Corporation | Flame retardant MPPE resin compositions |
IT1271419B (it) * | 1993-08-11 | 1997-05-28 | Himont Inc | Composizioni per fibre poliolefiniche aventi migliorate caratteristiche di resistenza alla fiamma ed assenza di corrosivita' |
US6989449B1 (en) * | 1999-09-15 | 2006-01-24 | Ciba Specialty Chemicals Corporation | Chlorohydrin and cationic compounds having high affinity for pulp or paper |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
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DE1181403B (de) * | 1959-12-24 | 1964-11-12 | Dow Chemical Co | Verfahren zur Herstellung von flammfesten Schaumstoffkoerpern aus thermoplastischen Polymeren von monovinylaromatischen Verbindungen |
DE1182810B (de) * | 1961-10-27 | 1964-12-03 | Basf Ag | Verfahren zum Flammwidrigmachen von Styrolpolymerisaten |
DE1193669B (de) * | 1962-06-09 | 1965-05-26 | Hoechst Ag | Selbstverloeschende Formmassen aus Olefin- oder Styrolpolymerisaten |
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US3058926A (en) * | 1958-07-24 | 1962-10-16 | Dow Chemical Co | Method for making self-extinguishing alkenyl aromatic resin compositions comprising incorporating therein an organic bromine-containing compound and an organic peroxide |
DE1494934B2 (de) * | 1963-02-19 | 1970-10-01 | Badische Anilin- & Soda-Fabrik Ag, 6700 Ludwigshafen | Schwerentflammbare feinteilige expandierbare Formmasse |
US3338864A (en) * | 1965-05-14 | 1967-08-29 | Wallace & Tiernan Inc | Flame retardant monoalkenyl benzene polymer compositions containing silane peroxy compounds |
-
0
- FR FR1486273D patent/FR1486273A/fr not_active Expired
-
1965
- 1965-07-09 DE DE1965B0082751 patent/DE1255302C2/de not_active Expired
-
1966
- 1966-07-07 GB GB30552/66A patent/GB1146653A/en not_active Expired
- 1966-07-08 US US563713A patent/US3457204A/en not_active Expired - Lifetime
- 1966-07-08 SE SE9413/66A patent/SE312434B/xx unknown
- 1966-07-08 NL NL6609646A patent/NL6609646A/xx unknown
- 1966-07-08 BR BR181120/66A patent/BR6681120D0/pt unknown
- 1966-07-08 LU LU51513A patent/LU51513A1/xx unknown
- 1966-07-08 IS IS1573A patent/IS1573A7/is unknown
- 1966-07-09 ES ES0328914A patent/ES328914A1/es not_active Expired
- 1966-07-11 BE BE683943D patent/BE683943A/xx unknown
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1181403B (de) * | 1959-12-24 | 1964-11-12 | Dow Chemical Co | Verfahren zur Herstellung von flammfesten Schaumstoffkoerpern aus thermoplastischen Polymeren von monovinylaromatischen Verbindungen |
DE1182810B (de) * | 1961-10-27 | 1964-12-03 | Basf Ag | Verfahren zum Flammwidrigmachen von Styrolpolymerisaten |
DE1193669B (de) * | 1962-06-09 | 1965-05-26 | Hoechst Ag | Selbstverloeschende Formmassen aus Olefin- oder Styrolpolymerisaten |
Also Published As
Publication number | Publication date |
---|---|
IS1573A7 (is) | 1966-10-08 |
FR1486273A (en, 2012) | 1967-10-05 |
ES328914A1 (es) | 1967-04-16 |
GB1146653A (en) | 1969-03-26 |
BR6681120D0 (pt) | 1973-07-03 |
BE683943A (en, 2012) | 1967-01-11 |
US3457204A (en) | 1969-07-22 |
NL6609646A (en, 2012) | 1967-01-10 |
DE1255302B (de) | 1967-11-30 |
LU51513A1 (en, 2012) | 1966-09-08 |
SE312434B (en, 2012) | 1969-07-14 |
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