NO761219L - - Google Patents
Info
- Publication number
- NO761219L NO761219L NO761219A NO761219A NO761219L NO 761219 L NO761219 L NO 761219L NO 761219 A NO761219 A NO 761219A NO 761219 A NO761219 A NO 761219A NO 761219 L NO761219 L NO 761219L
- Authority
- NO
- Norway
- Prior art keywords
- approx
- stated
- weight
- amount
- polyallyl compound
- Prior art date
Links
- 239000000178 monomer Substances 0.000 claims description 22
- 238000000034 method Methods 0.000 claims description 20
- 150000001875 compounds Chemical class 0.000 claims description 16
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 14
- 229920001155 polypropylene Polymers 0.000 claims description 14
- 229920005989 resin Polymers 0.000 claims description 12
- 239000011347 resin Substances 0.000 claims description 12
- 239000002245 particle Substances 0.000 claims description 9
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 9
- 238000010557 suspension polymerization reaction Methods 0.000 claims description 9
- 239000004606 Fillers/Extenders Substances 0.000 claims description 6
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 6
- 239000004641 Diallyl-phthalate Substances 0.000 claims description 5
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 claims description 5
- -1 compound phthalate Chemical class 0.000 claims description 5
- 229920000642 polymer Polymers 0.000 claims description 5
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 4
- 239000004800 polyvinyl chloride Substances 0.000 claims description 4
- 229920001577 copolymer Polymers 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
- PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical group C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000000047 product Substances 0.000 description 7
- 238000006116 polymerization reaction Methods 0.000 description 6
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 239000000375 suspending agent Substances 0.000 description 4
- 238000013019 agitation Methods 0.000 description 3
- 239000008367 deionised water Substances 0.000 description 3
- 229910021641 deionized water Inorganic materials 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 2
- 239000000443 aerosol Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 2
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 2
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 2
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- BJELTSYBAHKXRW-UHFFFAOYSA-N 2,4,6-triallyloxy-1,3,5-triazine Chemical compound C=CCOC1=NC(OCC=C)=NC(OCC=C)=N1 BJELTSYBAHKXRW-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- ATVJXMYDOSMEPO-UHFFFAOYSA-N 3-prop-2-enoxyprop-1-ene Chemical compound C=CCOCC=C ATVJXMYDOSMEPO-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 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
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- UBJVUCKUDDKUJF-UHFFFAOYSA-N Diallyl sulfide Chemical compound C=CCSCC=C UBJVUCKUDDKUJF-UHFFFAOYSA-N 0.000 description 1
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical compound [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920002153 Hydroxypropyl cellulose 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
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 1
- 229920003091 Methocel™ Polymers 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 229920001944 Plastisol Polymers 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- HOBNHEYUHWCGMG-UHFFFAOYSA-M [O-2].[OH-].O.O.O.[Cr+3] Chemical compound [O-2].[OH-].O.O.O.[Cr+3] HOBNHEYUHWCGMG-UHFFFAOYSA-M 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000005250 alkyl acrylate group Chemical group 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- ZPOLOEWJWXZUSP-AATRIKPKSA-N bis(prop-2-enyl) (e)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C\C(=O)OCC=C ZPOLOEWJWXZUSP-AATRIKPKSA-N 0.000 description 1
- ZPOLOEWJWXZUSP-WAYWQWQTSA-N bis(prop-2-enyl) (z)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C/C(=O)OCC=C ZPOLOEWJWXZUSP-WAYWQWQTSA-N 0.000 description 1
- FPODCVUTIPDRTE-UHFFFAOYSA-N bis(prop-2-enyl) hexanedioate Chemical compound C=CCOC(=O)CCCCC(=O)OCC=C FPODCVUTIPDRTE-UHFFFAOYSA-N 0.000 description 1
- BKXRKRANFLFTFU-UHFFFAOYSA-N bis(prop-2-enyl) oxalate Chemical compound C=CCOC(=O)C(=O)OCC=C BKXRKRANFLFTFU-UHFFFAOYSA-N 0.000 description 1
- IGBSAAYMSMEDQY-UHFFFAOYSA-N carboxy hydrogen carbonate;2-propan-2-ylperoxypropane Chemical compound OC(=O)OC(O)=O.CC(C)OOC(C)C IGBSAAYMSMEDQY-UHFFFAOYSA-N 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- ZWPVWTIRZYDPKW-UHFFFAOYSA-N chromium(VI) oxide peroxide Inorganic materials [O-2].[O-][Cr]([O-])(=O)=O ZWPVWTIRZYDPKW-UHFFFAOYSA-N 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- GYQQNCSTNDNVMM-UHFFFAOYSA-L disodium 4-(octadecylamino)-4-oxo-2-sulfobutanoate Chemical compound [Na+].[Na+].CCCCCCCCCCCCCCCCCCNC(=O)CC(C([O-])=O)S(O)(=O)=O.CCCCCCCCCCCCCCCCCCNC(=O)CC(C([O-])=O)S(O)(=O)=O GYQQNCSTNDNVMM-UHFFFAOYSA-L 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical group CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004999 plastisol Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- RTVVXRKGQRRXFJ-UHFFFAOYSA-N sodium;2-sulfobutanedioic acid Chemical compound [Na].OC(=O)CC(C(O)=O)S(O)(=O)=O RTVVXRKGQRRXFJ-UHFFFAOYSA-N 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- XHGIFBQQEGRTPB-UHFFFAOYSA-N tris(prop-2-enyl) phosphate Chemical compound C=CCOP(=O)(OCC=C)OCC=C XHGIFBQQEGRTPB-UHFFFAOYSA-N 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000007966 viscous suspension Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F14/00—Homopolymers and 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
- C08F14/02—Monomers containing chlorine
- C08F14/04—Monomers containing two carbon atoms
- C08F14/06—Vinyl chloride
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F214/00—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
- C08F214/02—Monomers containing chlorine
- C08F214/04—Monomers containing two carbon atoms
- C08F214/06—Vinyl chloride
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F255/00—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00
- C08F255/02—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00 on to polymers of olefins having two or three carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polymerisation Methods In General (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/567,328 US4031299A (en) | 1975-04-11 | 1975-04-11 | Process for forming a polyvinyl chloride extender resin by incorporating in the suspension polymerization medium a prehomogenized solution of a polyallyl compound and a low molecular polymer of propylene |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO761219L true NO761219L (de) | 1976-10-12 |
Family
ID=24266706
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO761219A NO761219L (de) | 1975-04-11 | 1976-04-08 |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US4031299A (de) |
| JP (1) | JPS51124188A (de) |
| AR (1) | AR210270A1 (de) |
| AU (1) | AU506244B2 (de) |
| BE (1) | BE840632A (de) |
| BR (1) | BR7601949A (de) |
| CS (1) | CS193072B2 (de) |
| DD (1) | DD125793A5 (de) |
| DE (1) | DE2608225A1 (de) |
| EG (1) | EG12655A (de) |
| FR (1) | FR2306998A1 (de) |
| GB (1) | GB1487991A (de) |
| HU (1) | HU172418B (de) |
| IL (1) | IL48998A (de) |
| NL (1) | NL7601939A (de) |
| NO (1) | NO761219L (de) |
| PH (1) | PH13730A (de) |
| PL (1) | PL105848B1 (de) |
| RO (1) | RO70268A (de) |
| SE (1) | SE410465B (de) |
| ZA (1) | ZA761297B (de) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS54134793A (en) * | 1978-04-12 | 1979-10-19 | Sumitomo Chem Co Ltd | Preparation of vinyl chloride resin |
| US4594376A (en) * | 1983-09-07 | 1986-06-10 | Showa Denko Kabushiki Kaisha | Propylene polymer composition |
| US5780564A (en) * | 1991-12-31 | 1998-07-14 | Topvin Oy | Method of preparing a homo-or copolymer of vinyl chloride containing .alpha. |
| FI95474C (fi) * | 1991-12-31 | 1996-02-12 | Topvin Oy | Vinyylikloridipolymeeri |
| FI95473C (fi) * | 1991-12-31 | 1996-02-12 | Topvin Oy | Työstöön valmis polyvinyylikloridi ja sen valmistusmenetelmä |
| US9334344B2 (en) | 2010-09-22 | 2016-05-10 | Vinnolit Gmbh & Co. Kg | Process for the production of a polyvinyl-chloride (PVC) resin |
| ES2400216T3 (es) | 2010-09-22 | 2013-04-08 | Vinnolit Gmbh & Co. Kg | Procedimiento para producir una resina de poli(cloruro de vinilo) (PVC) |
| KR102024141B1 (ko) * | 2016-06-21 | 2019-09-23 | 주식회사 엘지화학 | 염화비닐계 중합체의 제조방법 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE654644A (de) * | 1961-01-03 | |||
| US3468840A (en) * | 1964-08-18 | 1969-09-23 | Air Reduction | Vinyl chloride-ethylene copolymers and molding compositions containing said copolymers |
| GB1085114A (en) * | 1964-09-12 | 1967-09-27 | Sumitomo Chemical Co | Improvements in or relating to vinyl chloride polymers |
| US3468858A (en) * | 1964-12-31 | 1969-09-23 | Air Reduction | Vinyl chloride-propylene copolymers |
| FR1559743A (de) * | 1967-12-29 | 1969-03-14 | ||
| DE2006775A1 (de) * | 1970-02-14 | 1971-08-19 | Bayer Ag | Warmestabile Vinylchlorid Copoly mensate |
| GB1378391A (en) * | 1971-04-21 | 1974-12-27 | Bp Chem Int Ltd | Polymerisation process making same |
| US3816565A (en) * | 1972-05-08 | 1974-06-11 | Hooker Chemical Corp | Particle size control of bulk polymerized vinyl chloride polymers and copolymers |
| US3813373A (en) * | 1972-10-17 | 1974-05-28 | Sumitomo Chemical Co | Method for producing high bulk density polyvinyl chloride |
| US3838138A (en) * | 1972-11-16 | 1974-09-24 | Air Prod & Chem | Short cycle,thermally stable vinyl chloride-propylene copolymers |
-
1975
- 1975-04-11 US US05/567,328 patent/US4031299A/en not_active Expired - Lifetime
-
1976
- 1976-02-09 IL IL48998A patent/IL48998A/xx unknown
- 1976-02-12 SE SE7601599A patent/SE410465B/xx unknown
- 1976-02-13 AU AU11115/76A patent/AU506244B2/en not_active Expired
- 1976-02-25 AR AR262376A patent/AR210270A1/es active
- 1976-02-25 NL NL7601939A patent/NL7601939A/xx not_active Application Discontinuation
- 1976-02-28 DE DE19762608225 patent/DE2608225A1/de active Pending
- 1976-03-02 GB GB8251/76A patent/GB1487991A/en not_active Expired
- 1976-03-03 ZA ZA761297A patent/ZA761297B/xx unknown
- 1976-03-10 EG EG145/76A patent/EG12655A/xx active
- 1976-03-17 FR FR7607684A patent/FR2306998A1/fr active Granted
- 1976-03-25 PL PL1976188216A patent/PL105848B1/pl unknown
- 1976-03-31 BR BR7601949A patent/BR7601949A/pt unknown
- 1976-04-01 RO RO7685380A patent/RO70268A/ro unknown
- 1976-04-07 JP JP51039145A patent/JPS51124188A/ja active Pending
- 1976-04-07 HU HU76SA00002912A patent/HU172418B/hu unknown
- 1976-04-08 PH PH15318A patent/PH13730A/en unknown
- 1976-04-08 CS CS762331A patent/CS193072B2/cs unknown
- 1976-04-08 NO NO761219A patent/NO761219L/no unknown
- 1976-04-09 BE BE7000802A patent/BE840632A/xx unknown
- 1976-04-09 DD DD192300A patent/DD125793A5/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| SE7601599L (sv) | 1976-10-12 |
| US4031299A (en) | 1977-06-21 |
| IL48998A (en) | 1978-09-29 |
| DD125793A5 (de) | 1977-05-18 |
| FR2306998A1 (fr) | 1976-11-05 |
| RO70268A (ro) | 1982-03-24 |
| BR7601949A (pt) | 1976-10-05 |
| GB1487991A (en) | 1977-10-05 |
| PH13730A (en) | 1980-09-09 |
| BE840632A (nl) | 1976-10-11 |
| PL105848B1 (pl) | 1979-11-30 |
| EG12655A (en) | 1979-06-30 |
| ZA761297B (en) | 1977-02-23 |
| HU172418B (hu) | 1978-08-28 |
| AU506244B2 (en) | 1979-12-20 |
| JPS51124188A (en) | 1976-10-29 |
| AR210270A1 (es) | 1977-07-15 |
| AU1111576A (en) | 1977-08-18 |
| SE410465B (sv) | 1979-10-15 |
| NL7601939A (nl) | 1976-10-13 |
| DE2608225A1 (de) | 1976-10-21 |
| IL48998A0 (en) | 1976-04-30 |
| CS193072B2 (en) | 1979-09-17 |
| FR2306998B1 (de) | 1980-05-16 |
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