NO773806L - Vinylklorid- og vinylidenkloridpolymerpreparater - Google Patents

Vinylklorid- og vinylidenkloridpolymerpreparater

Info

Publication number: NO773806L
Authority: NO; Norway
Prior art keywords: approx; parts; weight; vinyl; polymer
Prior art date: 1977-02-22

Application number

NO773806A

Other languages

English (en)

Norwegian (no)

Inventor

Joachim Ernst Hartitz

Original Assignee

Goodrich Co B F

Priority date (The priority date 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 date listed.)

1977-02-22

Filing date

1977-11-07

Publication date

1978-08-23

1977-11-07 Application filed by Goodrich Co B F filed Critical Goodrich Co B F

1978-08-23 Publication of NO773806L publication Critical patent/NO773806L/no

Links

BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 title claims description 14
LGXVIGDEPROXKC-UHFFFAOYSA-N 1,1-dichloroethene Chemical compound ClC(Cl)=C LGXVIGDEPROXKC-UHFFFAOYSA-N 0.000 title 1
238000002360 preparation method Methods 0.000 title 1
229920000642 polymer Polymers 0.000 claims description 35
239000000779 smoke Substances 0.000 claims description 25
239000000203 mixture Substances 0.000 claims description 17
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 11
239000000178 monomer Substances 0.000 claims description 10
150000002148 esters Chemical class 0.000 claims description 8
239000002245 particle Substances 0.000 claims description 8
125000004432 carbon atom Chemical group C* 0.000 claims description 6
150000001735 carboxylic acids Chemical class 0.000 claims description 6
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 4
150000001408 amides Chemical class 0.000 claims description 3
230000015572 biosynthetic process Effects 0.000 claims description 3
238000002485 combustion reaction Methods 0.000 claims description 3
229920001567 vinyl ester resin Polymers 0.000 claims description 3
150000002238 fumaric acids Chemical class 0.000 claims 1
150000002689 maleic acids Chemical class 0.000 claims 1
-1 polyethylene Polymers 0.000 description 7
LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 4
WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 4
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 4
BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 4
150000001875 compounds Chemical class 0.000 description 4
238000000034 method Methods 0.000 description 4
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 4
239000003638 chemical reducing agent Substances 0.000 description 3
239000004615 ingredient Substances 0.000 description 3
239000000463 material Substances 0.000 description 3
239000000843 powder Substances 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
LEJBBGNFPAFPKQ-UHFFFAOYSA-N 2-(2-prop-2-enoyloxyethoxy)ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOC(=O)C=C LEJBBGNFPAFPKQ-UHFFFAOYSA-N 0.000 description 2
GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 2
FWWXYLGCHHIKNY-UHFFFAOYSA-N 2-ethoxyethyl prop-2-enoate Chemical compound CCOCCOC(=O)C=C FWWXYLGCHHIKNY-UHFFFAOYSA-N 0.000 description 2
HFCUBKYHMMPGBY-UHFFFAOYSA-N 2-methoxyethyl prop-2-enoate Chemical compound COCCOC(=O)C=C HFCUBKYHMMPGBY-UHFFFAOYSA-N 0.000 description 2
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
KWCPPCKBBRBYEE-UHFFFAOYSA-N 3-chloropropyl prop-2-enoate Chemical compound ClCCCOC(=O)C=C KWCPPCKBBRBYEE-UHFFFAOYSA-N 0.000 description 2
HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 2
229910000014 Bismuth subcarbonate Inorganic materials 0.000 description 2
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 2
VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
239000000654 additive Substances 0.000 description 2
230000000996 additive effect Effects 0.000 description 2
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
MGLUJXPJRXTKJM-UHFFFAOYSA-L bismuth subcarbonate Chemical compound O=[Bi]OC(=O)O[Bi]=O MGLUJXPJRXTKJM-UHFFFAOYSA-L 0.000 description 2
229940036358 bismuth subcarbonate Drugs 0.000 description 2
FUSUHKVFWTUUBE-UHFFFAOYSA-N buten-2-one Chemical compound CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 2
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
KBLWLMPSVYBVDK-UHFFFAOYSA-N cyclohexyl prop-2-enoate Chemical compound C=CC(=O)OC1CCCCC1 KBLWLMPSVYBVDK-UHFFFAOYSA-N 0.000 description 2
150000001993 dienes Chemical class 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
XJELOQYISYPGDX-UHFFFAOYSA-N ethenyl 2-chloroacetate Chemical compound ClCC(=O)OC=C XJELOQYISYPGDX-UHFFFAOYSA-N 0.000 description 2
GLVVKKSPKXTQRB-UHFFFAOYSA-N ethenyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OC=C GLVVKKSPKXTQRB-UHFFFAOYSA-N 0.000 description 2
UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 2
239000001530 fumaric acid Substances 0.000 description 2
LNMQRPPRQDGUDR-UHFFFAOYSA-N hexyl prop-2-enoate Chemical compound CCCCCCOC(=O)C=C LNMQRPPRQDGUDR-UHFFFAOYSA-N 0.000 description 2
PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 2
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
239000011976 maleic acid Substances 0.000 description 2
238000002156 mixing Methods 0.000 description 2
FSAJWMJJORKPKS-UHFFFAOYSA-N octadecyl prop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C=C FSAJWMJJORKPKS-UHFFFAOYSA-N 0.000 description 2
RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 2
HVAMZGADVCBITI-UHFFFAOYSA-M pent-4-enoate Chemical compound [O-]C(=O)CCC=C HVAMZGADVCBITI-UHFFFAOYSA-M 0.000 description 2
PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 2
WRAQQYDMVSCOTE-UHFFFAOYSA-N phenyl prop-2-enoate Chemical compound C=CC(=O)OC1=CC=CC=C1 WRAQQYDMVSCOTE-UHFFFAOYSA-N 0.000 description 2
238000003825 pressing Methods 0.000 description 2
239000000725 suspension Substances 0.000 description 2
150000004684 trihydrates Chemical class 0.000 description 2
229920002554 vinyl polymer Polymers 0.000 description 2
PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical group C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 description 1
OZCMOJQQLBXBKI-UHFFFAOYSA-N 1-ethenoxy-2-methylpropane Chemical compound CC(C)COC=C OZCMOJQQLBXBKI-UHFFFAOYSA-N 0.000 description 1
UZKWTJUDCOPSNM-UHFFFAOYSA-N 1-ethenoxybutane Chemical compound CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical compound C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 description 1
HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 1
RFIMISVNSAUMBU-UHFFFAOYSA-N 2-(hydroxymethyl)-2-(prop-2-enoxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC=C RFIMISVNSAUMBU-UHFFFAOYSA-N 0.000 description 1
SBYMUDUGTIKLCR-UHFFFAOYSA-N 2-chloroethenylbenzene Chemical compound ClC=CC1=CC=CC=C1 SBYMUDUGTIKLCR-UHFFFAOYSA-N 0.000 description 1
OMPKRANXQGIMCT-UHFFFAOYSA-N 2-cyanopropyl prop-2-enoate Chemical class N#CC(C)COC(=O)C=C OMPKRANXQGIMCT-UHFFFAOYSA-N 0.000 description 1
HKFPXINKVCOLOD-UHFFFAOYSA-N 2-hexylsulfanylethyl prop-2-enoate Chemical compound CCCCCCSCCOC(=O)C=C HKFPXINKVCOLOD-UHFFFAOYSA-N 0.000 description 1
UHBAWOXYQROEIH-UHFFFAOYSA-N 3-chloro-4-(2-chlorobut-3-enoxy)but-1-ene Chemical compound C=CC(Cl)COCC(Cl)C=C UHBAWOXYQROEIH-UHFFFAOYSA-N 0.000 description 1
FASUFOTUSHAIHG-UHFFFAOYSA-N 3-methoxyprop-1-ene Chemical compound COCC=C FASUFOTUSHAIHG-UHFFFAOYSA-N 0.000 description 1
DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 1
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
ICQVTDZLHBCFON-UHFFFAOYSA-N C(C=C)(=S)OCCCCCC Chemical compound C(C=C)(=S)OCCCCCC ICQVTDZLHBCFON-UHFFFAOYSA-N 0.000 description 1
GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
239000004743 Polypropylene Substances 0.000 description 1
QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
125000003342 alkenyl 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
229910000410 antimony oxide Inorganic materials 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
230000005540 biological transmission Effects 0.000 description 1
150000001622 bismuth compounds Chemical class 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
RNFNDJAIBTYOQL-UHFFFAOYSA-N chloral hydrate Chemical compound OC(O)C(Cl)(Cl)Cl RNFNDJAIBTYOQL-UHFFFAOYSA-N 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
125000004386 diacrylate group Chemical group 0.000 description 1
UOCIZHQMWNPGEN-UHFFFAOYSA-N dialuminum;oxygen(2-);trihydrate Chemical compound O.O.O.[O-2].[O-2].[O-2].[Al+3].[Al+3] UOCIZHQMWNPGEN-UHFFFAOYSA-N 0.000 description 1
238000001035 drying Methods 0.000 description 1
238000005530 etching Methods 0.000 description 1
ZTWTYVWXUKTLCP-UHFFFAOYSA-L ethenyl-dioxido-oxo-$l^{5}-phosphane Chemical compound [O-]P([O-])(=O)C=C ZTWTYVWXUKTLCP-UHFFFAOYSA-L 0.000 description 1
125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
229940052303 ethers for general anesthesia Drugs 0.000 description 1
SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000003063 flame retardant Substances 0.000 description 1
VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
239000008187 granular material Substances 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
ZIUHHBKFKCYYJD-UHFFFAOYSA-N n,n'-methylenebisacrylamide Chemical compound C=CC(=O)NCNC(=O)C=C ZIUHHBKFKCYYJD-UHFFFAOYSA-N 0.000 description 1
150000002816 nickel compounds Chemical class 0.000 description 1
JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 description 1
VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000004033 plastic Substances 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
239000004800 polyvinyl chloride Substances 0.000 description 1
229920000915 polyvinyl chloride Polymers 0.000 description 1
238000001556 precipitation 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
238000011084 recovery Methods 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
238000005096 rolling process Methods 0.000 description 1
239000000243 solution Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
230000001629 suppression Effects 0.000 description 1
238000010998 test method Methods 0.000 description 1
BIKXLKXABVUSMH-UHFFFAOYSA-N trizinc;diborate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]B([O-])[O-].[O-]B([O-])[O-] BIKXLKXABVUSMH-UHFFFAOYSA-N 0.000 description 1
229960000834 vinyl ether Drugs 0.000 description 1
239000011787 zinc oxide 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
- 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
- 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
- C08K3/24—Acids; Salts thereof
- C08K3/26—Carbonates; Bicarbonates

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)
Medicinal Preparation (AREA)

NO773806A 1977-02-22 1977-11-07 Vinylklorid- og vinylidenkloridpolymerpreparater NO773806L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US05/770,326 US4143030A (en)	1977-02-22	1977-02-22	Smoke retardant vinyl chloride and vinylidene chloride polymer compositions

Publications (1)

Publication Number	Publication Date
NO773806L true NO773806L (no)	1978-08-23

Family

ID=25088172

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO773806A NO773806L (no)	1977-02-22	1977-11-07	Vinylklorid- og vinylidenkloridpolymerpreparater

Country Status (15)

Country	Link
US (1)	US4143030A (da)
JP (1)	JPS53105554A (da)
AU (1)	AU511018B2 (da)
BE (1)	BE859763A (da)
CA (1)	CA1090944A (da)
DE (1)	DE2745828A1 (da)
DK (1)	DK452477A (da)
FR (1)	FR2381084A1 (da)
GB (1)	GB1575333A (da)
IT (1)	IT1087962B (da)
NL (1)	NL7800022A (da)
NO (1)	NO773806L (da)
NZ (1)	NZ185387A (da)
SE (1)	SE7711348L (da)
ZA (1)	ZA775998B (da)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS54114558A (en) *	1978-02-28	1979-09-06	Shin Etsu Chem Co Ltd	Flame-retardant vinyl chloride resin composition
DE3275651D1 (en) *	1981-11-19	1987-04-16	M & T Chemicals Inc	Small particle size hydrated alumina as an impact synergist for impact modified vinyl halide polymers
IT1170103B (it) *	1983-01-25	1987-06-03	Umberto Crespi	Compound di pvc plastificato e/o non, atossico e/o non, senza emissione di fumi, corrosivi e non, durante le lavorazioni di trasformazione
US4808459A (en) *	1987-09-16	1989-02-28	Collins & Aikman Corporation	Carpet with polyvinylidene chloride latex tuft-lock adhesive coating
JP2766926B2 (ja) *	1988-10-13	1998-06-18	丸菱油化工業株式会社	防炎、耐透湿性水性被覆材料

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1420978A (en) *	1972-03-24	1976-01-14	Bicc Ltd	Polymer compositions and electric cables made with them
JPS5139986B2 (da) *	1974-08-19	1976-10-30
AR207876A1 (es) *	1974-10-28	1976-11-08	Montedison Spa	Composiciones poliolefinicas aptas para producir articulos autoextinguentes y articulos con ellas obtenidos
US3975359A (en) *	1974-12-30	1976-08-17	The B. F. Goodrich Company	Smoke retardant vinyl chloride and vinylidene chloride polymer compositions
US3985706A (en) *	1975-03-24	1976-10-12	The Firestone Tire & Rubber Company	Smoke-retardant for chlorinated polyethylene and vinyl chloride polymers
US3957723A (en) *	1975-06-27	1976-05-18	The Firestone Tire & Rubber Company	Flame and smoke retardants for polyvinyl chloride

1977
- 1977-02-22 US US05/770,326 patent/US4143030A/en not_active Expired - Lifetime
- 1977-10-05 CA CA288,156A patent/CA1090944A/en not_active Expired
- 1977-10-06 ZA ZA00775998A patent/ZA775998B/xx unknown
- 1977-10-07 AU AU29473/77A patent/AU511018B2/en not_active Expired
- 1977-10-07 GB GB41770/77A patent/GB1575333A/en not_active Expired
- 1977-10-07 NZ NZ185387A patent/NZ185387A/xx unknown
- 1977-10-10 SE SE7711348A patent/SE7711348L/xx unknown
- 1977-10-12 DK DK452477A patent/DK452477A/da not_active Application Discontinuation
- 1977-10-12 DE DE19772745828 patent/DE2745828A1/de not_active Withdrawn
- 1977-10-14 BE BE181776A patent/BE859763A/xx unknown
- 1977-10-14 IT IT28645/77A patent/IT1087962B/it active
- 1977-10-24 FR FR7731989A patent/FR2381084A1/fr not_active Withdrawn
- 1977-10-27 JP JP12822477A patent/JPS53105554A/ja active Pending
- 1977-11-07 NO NO773806A patent/NO773806L/no unknown
1978
- 1978-01-02 NL NL7800022A patent/NL7800022A/xx not_active Application Discontinuation

Also Published As

Publication number	Publication date
CA1090944A (en)	1980-12-02
JPS53105554A (en)	1978-09-13
AU2947377A (en)	1979-04-12
IT1087962B (it)	1985-06-04
NZ185387A (en)	1979-03-16
NL7800022A (nl)	1978-08-24
BE859763A (fr)	1978-02-01
ZA775998B (en)	1978-05-30
AU511018B2 (en)	1980-07-24
DK452477A (da)	1978-08-23
SE7711348L (sv)	1978-08-22
US4143030A (en)	1979-03-06
FR2381084A1 (fr)	1978-09-15
DE2745828A1 (de)	1978-08-24
GB1575333A (en)	1980-09-17

Publication	Publication Date	Title
US3965068A (en)	1976-06-22	Smoke retardant vinyl chloride and vinylidene chloride polymer compositions
JPH04233964A (ja)	1992-08-21	高靱性の熱可塑性ポリオキシメチレン成形組成物及びその用途
EP0042091B1 (de)	1985-01-16	Kerbschlagzähe Vinylchloridpolymerisate
NO773806L (no)	1978-08-23	Vinylklorid- og vinylidenkloridpolymerpreparater
US4507414A (en)	1985-03-26	Smoke retardant vinyl halide polymer compositions
US3975356A (en)	1976-08-17	Smoke retardant vinyl chloride and vinylidene chloride polymer compositions
CA1087783A (en)	1980-10-14	Smoke retardant vinyl chloride and vinylidene chloride polymer compositions
DE2257103C2 (de)	1982-12-09	Schwerentflammbares, schlagfestes Polymerisatgemisch
EP0459147B1 (de)	1995-11-15	Expandierbare Styrolpolymerisate
US3962163A (en)	1976-06-08	Smoke retardant vinyl chloride and vinylidene chloride polymer compositions
US3975359A (en)	1976-08-17	Smoke retardant vinyl chloride and vinylidene chloride polymer compositions
US3058927A (en)	1962-10-16	Self-extinguishing thermoplastic alkenyl aromatic polymer composition containing ammonium bromide, an anticorrosion agent, and a di (aralkyl) peroxide and method of preparing same
CA1067228A (en)	1979-11-27	Smoke retardant vinyl chloride and vinylidene chloride polymer compositions
DE2148224C2 (de)	1982-10-28	Verwendung von wässrigen Polymerisatdispersionen zur Umhüllung von Granulaten aus Äthylen/Vinylacetat-Copolymerisaten
EP4077481A1 (de)	2022-10-26	Flammgeschützte copolymere und formmassen
JPH0425302B2 (da)	1992-04-30
US3878167A (en)	1975-04-15	Flame and smoke retardant vinyl chloride and vinylidene chloride polymer compositions
WO1995015994A1 (de)	1995-06-15	Plastisolzusammensetzung
JPH11335481A (ja)	1999-12-07	抗菌性発泡樹脂粒子及びその成形体
US3970638A (en)	1976-07-20	Smoke retardant vinyl chloride and vinylidene chloride polymer compositions
US3968064A (en)	1976-07-06	Smoke retardant vinyl chloride and vinylidene chloride polymer compositions
DE2257066C2 (de)	1982-09-16	Schwerentflammbares, schlagfestes Polymerisatgemisch
IL33893A (en)	1973-07-30	Method of imparting the feature of self-extinguishing to polyvinyl chloride whose resistance to infection has changed
US4234472A (en)	1980-11-18	Smoke retardant vinyl chloride and vinylidene chloride polymer compositions
EP1151015B1 (de)	2002-05-29	Verfahren zur minderung der geruchsemission wässriger schutzkolloid-stabilisierter vinylaromat-1,3-dien-copolymerisatdispersionen