NO121808B - - Google Patents

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Info

Publication number: NO121808B
Authority: NO; Norway
Prior art keywords: ethylene; vessel; solution; vinyl acetate; aqueous
Prior art date: 1966-04-20

Application number

NO167771A

Other languages

English (en)

Norwegian (no)

Inventor

F Gintz

Original Assignee

Bp Chemicals Ltd Gb

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.)

1966-04-20

Filing date

1967-04-18

Publication date

1971-04-13

1967-04-18 Application filed by Bp Chemicals Ltd Gb filed Critical Bp Chemicals Ltd Gb

1971-04-13 Publication of NO121808B publication Critical patent/NO121808B/no

Links

VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 38
239000005977 Ethylene Substances 0.000 claims description 38
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 21
229920001577 copolymer Polymers 0.000 claims description 21
239000006185 dispersion Substances 0.000 claims description 21
238000006116 polymerization reaction Methods 0.000 claims description 20
239000008346 aqueous phase Substances 0.000 claims description 12
238000000034 method Methods 0.000 claims description 12
238000006243 chemical reaction Methods 0.000 claims description 8
239000000084 colloidal system Substances 0.000 claims description 4
239000011953 free-radical catalyst Substances 0.000 claims description 4
239000007788 liquid Substances 0.000 claims description 4
239000004094 surface-active agent Substances 0.000 claims description 4
230000001681 protective effect Effects 0.000 claims description 3
238000007720 emulsion polymerization reaction Methods 0.000 claims 1
239000000243 solution Substances 0.000 description 22
239000000178 monomer Substances 0.000 description 13
239000000839 emulsion Substances 0.000 description 12
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
239000003054 catalyst Substances 0.000 description 10
239000004816 latex Substances 0.000 description 9
229920000126 latex Polymers 0.000 description 9
150000001875 compounds Chemical class 0.000 description 8
-1 alkali metal chlorate Chemical class 0.000 description 7
239000000203 mixture Substances 0.000 description 6
238000003860 storage Methods 0.000 description 6
229910052757 nitrogen Inorganic materials 0.000 description 5
229910052783 alkali metal Inorganic materials 0.000 description 4
230000015572 biosynthetic process Effects 0.000 description 4
150000002148 esters Chemical class 0.000 description 4
239000007789 gas Substances 0.000 description 4
238000007792 addition Methods 0.000 description 3
ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 3
239000012071 phase Substances 0.000 description 3
239000000376 reactant Substances 0.000 description 3
230000001105 regulatory effect Effects 0.000 description 3
229920001567 vinyl ester resin Polymers 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
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 2
IGFHQQFPSIBGKE-UHFFFAOYSA-N 4-nonylphenol Chemical compound CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 2
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
238000010924 continuous production Methods 0.000 description 2
WBZKQQHYRPRKNJ-UHFFFAOYSA-L disulfite Chemical compound [O-]S(=O)S([O-])(=O)=O WBZKQQHYRPRKNJ-UHFFFAOYSA-L 0.000 description 2
150000004698 iron complex Chemical class 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
238000002156 mixing Methods 0.000 description 2
239000012047 saturated solution Substances 0.000 description 2
HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 2
235000010262 sodium metabisulphite Nutrition 0.000 description 2
239000007787 solid Substances 0.000 description 2
238000003756 stirring Methods 0.000 description 2
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
FRQQKWGDKVGLFI-UHFFFAOYSA-N 2-methylundecane-2-thiol Chemical compound CCCCCCCCCC(C)(C)S FRQQKWGDKVGLFI-UHFFFAOYSA-N 0.000 description 1
DYBIGIADVHIODH-UHFFFAOYSA-N 2-nonylphenol;oxirane Chemical compound C1CO1.CCCCCCCCCC1=CC=CC=C1O DYBIGIADVHIODH-UHFFFAOYSA-N 0.000 description 1
239000004160 Ammonium persulphate 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
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical group C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
239000001856 Ethyl cellulose Substances 0.000 description 1
ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
WERKSKAQRVDLDW-ANOHMWSOSA-N [(2s,3r,4r,5r)-2,3,4,5,6-pentahydroxyhexyl] (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO WERKSKAQRVDLDW-ANOHMWSOSA-N 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
229910001870 ammonium persulfate Inorganic materials 0.000 description 1
235000019395 ammonium persulphate Nutrition 0.000 description 1
150000001449 anionic compounds Chemical class 0.000 description 1
235000019400 benzoyl peroxide Nutrition 0.000 description 1
JZQAAQZDDMEFGZ-UHFFFAOYSA-N bis(ethenyl) hexanedioate Chemical compound C=COC(=O)CCCCC(=O)OC=C JZQAAQZDDMEFGZ-UHFFFAOYSA-N 0.000 description 1
238000007664 blowing Methods 0.000 description 1
229910052796 boron Inorganic materials 0.000 description 1
239000000872 buffer Substances 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
229920003086 cellulose ether Polymers 0.000 description 1
XTEGARKTQYYJKE-UHFFFAOYSA-M chlorate Inorganic materials [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
239000008199 coating composition Substances 0.000 description 1
230000008602 contraction Effects 0.000 description 1
LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
230000007423 decrease Effects 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
150000001991 dicarboxylic acids Chemical class 0.000 description 1
235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 description 1
YHAIUSTWZPMYGG-UHFFFAOYSA-L disodium;2,2-dioctyl-3-sulfobutanedioate Chemical compound [Na+].[Na+].CCCCCCCCC(C([O-])=O)(C(C([O-])=O)S(O)(=O)=O)CCCCCCCC YHAIUSTWZPMYGG-UHFFFAOYSA-L 0.000 description 1
238000006073 displacement reaction Methods 0.000 description 1
WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 1
229920001249 ethyl cellulose Polymers 0.000 description 1
235000019325 ethyl cellulose Nutrition 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000001530 fumaric acid Substances 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
239000011261 inert gas Substances 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
150000008040 ionic compounds Chemical class 0.000 description 1
150000004668 long chain fatty acids Chemical class 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
150000004978 peroxycarbonates Chemical class 0.000 description 1
JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
235000019422 polyvinyl alcohol Nutrition 0.000 description 1
229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
235000015497 potassium bicarbonate Nutrition 0.000 description 1
239000011736 potassium bicarbonate Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
BWJUFXUULUEGMA-UHFFFAOYSA-N propan-2-yl propan-2-yloxycarbonyloxy carbonate Chemical compound CC(C)OC(=O)OOC(=O)OC(C)C BWJUFXUULUEGMA-UHFFFAOYSA-N 0.000 description 1
238000010526 radical polymerization reaction Methods 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
ZIWRUEGECALFST-UHFFFAOYSA-M sodium 4-(4-dodecoxysulfonylphenoxy)benzenesulfonate Chemical compound [Na+].CCCCCCCCCCCCOS(=O)(=O)c1ccc(Oc2ccc(cc2)S([O-])(=O)=O)cc1 ZIWRUEGECALFST-UHFFFAOYSA-M 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
235000017557 sodium bicarbonate Nutrition 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
229940001584 sodium metabisulfite Drugs 0.000 description 1
239000004296 sodium metabisulphite Substances 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
239000003381 stabilizer Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 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
- C08F218/00—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 an acyloxy radical of a saturated carboxylic acid, of carbonic acid or of a haloformic acid
- C08F218/02—Esters of monocarboxylic acids
- C08F218/04—Vinyl esters
- 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
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond

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)
Compositions Of Macromolecular Compounds (AREA)
Processes Of Treating Macromolecular Substances (AREA)

NO167771A 1966-04-20 1967-04-18 NO121808B (zh)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB17216/66A GB1133126A (en)	1966-04-20	1966-04-20	Process for the manufacture of stable aqueous dispersions of vinyl esters of organicacids and ethylene

Publications (1)

Publication Number	Publication Date
NO121808B true NO121808B (zh)	1971-04-13

Family

ID=10091272

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO167771A NO121808B (zh)	1966-04-20	1967-04-18

Country Status (9)

Country	Link
US (1)	US3532658A (zh)
BE (1)	BE697308A (zh)
DE (1)	DE1720467A1 (zh)
ES (1)	ES339492A1 (zh)
FI (1)	FI46624C (zh)
GB (1)	GB1133126A (zh)
NL (2)	NL6704604A (zh)
NO (1)	NO121808B (zh)
SE (1)	SE337686B (zh)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3661696A (en) *	1970-09-30	1972-05-09	Union Oil Co	Ethylene-vinyl acetate copolymer adhesive composition and method of preparation
DE2214410C3 (de) *	1972-03-24	1978-10-12	Hoechst Ag, 6000 Frankfurt	Verfahren zur Herstellung eines redispergierbaren Vinylacetat/Äthylen-Polymerdispersionspulvers
JPS603087B2 (ja) *	1976-06-17	1985-01-25	住友化学工業株式会社	水性分散液の製造方法
DE3008748A1 (de) *	1980-03-07	1981-09-24	Bayer Ag, 5090 Leverkusen	Verfahren zur herstellung von ethylen-venylester-pfropfpolymerisatdispersionen
US4476286A (en) *	1981-09-25	1984-10-09	Ppg Industries, Inc.	Thermosetting cationic latex compositions containing aminoplast curing agents
US4380601A (en) *	1981-09-25	1983-04-19	Ppg Industries, Inc.	Thermosetting catonic acrylic latices and their use in coating compositions
US4399254A (en) *	1981-09-25	1983-08-16	Ppg Industries, Inc.	Cationic latices useful for thermoplastic and thermosetting applications
US4921898A (en) *	1985-08-02	1990-05-01	Air Products And Chemicals, Inc.	Vinyl acetate-ethylene copolymer emulsions prepared in the presence of a stabilizing system of a low molecular weight polyvinyl alcohol and a surfactant
DE3535389A1 (de) *	1985-10-03	1987-04-09	Wacker Chemie Gmbh	Verfahren zur herstellung von bindemitteln fuer anstrichfarben und putze
JPH086003B2 (ja) *	1987-09-01	1996-01-24	コニシ株式会社	酢酸ビニル樹脂エマルジョン組成物
DE19531515B4 (de) *	1995-08-26	2005-12-22	Celanese Emulsions Gmbh	Herstellung von Polyvinylester-Dispersionen
DE10035587A1 (de)	2000-07-21	2002-02-07	Wacker Polymer Systems Gmbh	Verfahren zur Herstellung von Schutzkolloid-stabilisierten Polymerisaten mittels kontinuierlicher Emulsionspolymerisation

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3296170A (en) *	1963-04-03	1967-01-03	Union Carbide Corp	Emulsion polymerization of ethylene

0
- NL NL135330D patent/NL135330C/xx active
1966
- 1966-04-20 GB GB17216/66A patent/GB1133126A/en not_active Expired
1967
- 1967-03-22 US US625065A patent/US3532658A/en not_active Expired - Lifetime
- 1967-03-31 NL NL6704604A patent/NL6704604A/xx unknown
- 1967-04-05 FI FI670999A patent/FI46624C/fi active
- 1967-04-12 DE DE19671720467 patent/DE1720467A1/de active Pending
- 1967-04-17 SE SE05341/67A patent/SE337686B/xx unknown
- 1967-04-18 NO NO167771A patent/NO121808B/no unknown
- 1967-04-19 ES ES339492A patent/ES339492A1/es not_active Expired
- 1967-04-20 BE BE697308D patent/BE697308A/xx unknown

Also Published As

Publication number	Publication date
FI46624C (fi)	1973-05-08
ES339492A1 (es)	1968-05-01
NL135330C (zh)
SE337686B (zh)	1971-08-16
FI46624B (zh)	1973-01-31
DE1720467A1 (de)	1970-03-12
US3532658A (en)	1970-10-06
NL6704604A (zh)	1967-10-23
BE697308A (zh)	1967-10-20
GB1133126A (en)	1968-11-06

Publication	Publication Date	Title
US6255384B1 (en)	2001-07-03	Method of manufacturing fluoropolymers
NO121808B (zh)	1971-04-13
US3501440A (en)	1970-03-17	Process for preparing vinyl chloride/ethylene copolymers
WO1997017381A9 (en)	1997-09-18	Method of manufacturing fluoropolymers
US2468054A (en)	1949-04-26	Copolymers of vinylidene fluoride with ethylene and halogenated ethylenes
US6245851B1 (en)	2001-06-12	Vinyl acetate/ethylene high solids emulsions
EP0460936A1 (en)	1991-12-11	Methanol copolymerization of ethylene
US3954698A (en)	1976-05-04	Polymerisation process
US3983096A (en)	1976-09-28	Polymerization process under pressure in an annular equipment
NO823346L (no)	1983-04-07	Fremgangsmaate ved fremstilling av vandige copolymer-dispersjoner og anvendelse derav
NO140937B (no)	1979-09-03	Fremgangsmaate ved bleking av cellulosemasse
GB703253A (en)	1954-02-03	A process for the preparation of copolymers and compositions containing the same
US3163628A (en)	1964-12-29	Polymerization process for unsaturated fluoroolefins
NO138622B (no)	1978-07-03	Anordning i lufteledningene fra oljetanker paa skip
DE2521766C2 (de)	1984-06-28	Mischpolymere und Verfahren zu deren Herstellung
US4816534A (en)	1989-03-28	Preparation of vinylpyrrolidone polymers
US3963687A (en)	1976-06-15	Two step continuous polymerization method to form acrylonitrile copolymers
US2404817A (en)	1946-07-30	Production of copolymers of monoethenoid compounds
KR20080106235A (ko)	2008-12-04	비닐 클로라이드 (코)폴리머의 연속 제조 방법
US2507568A (en)	1950-05-16	Telomers of monoolefins and saturated halogenated carboxylic acids, esters, and anhydrides
US4009140A (en)	1977-02-22	Clear ethylene polymer emulsions having light transmission of at least 95% and polishes containing the same
US3642754A (en)	1972-02-15	Process for polymerizing fluoro-olefins in the presence of isobutyryl peroxide
US2616881A (en)	1952-11-04	Shortstopping vinyl chloride polymerizations with ethylenically-unsaturated ketones
ES2599581T3 (es)	2017-02-02	Procedimiento continuo para la producción de (co)polímeros de cloruro de vinilo
JPH0321561B2 (zh)	1991-03-25