NO742239L - - Google Patents
Info
- Publication number
- NO742239L NO742239L NO742239A NO742239A NO742239L NO 742239 L NO742239 L NO 742239L NO 742239 A NO742239 A NO 742239A NO 742239 A NO742239 A NO 742239A NO 742239 L NO742239 L NO 742239L
- Authority
- NO
- Norway
- Prior art keywords
- interpolymer
- irradiation
- copolymer
- hydrolyzed
- vinyl acetate
- Prior art date
Links
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 60
- 238000000034 method Methods 0.000 claims description 30
- 238000006460 hydrolysis reaction Methods 0.000 claims description 25
- 229920001577 copolymer Polymers 0.000 claims description 24
- 229920001567 vinyl ester resin Polymers 0.000 claims description 22
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical group CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 20
- 230000007062 hydrolysis Effects 0.000 claims description 19
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical group [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 claims description 16
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 14
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 claims description 13
- 229910052753 mercury Inorganic materials 0.000 claims description 13
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 12
- 239000005977 Ethylene Substances 0.000 claims description 12
- -1 alkali metal alkoxide Chemical class 0.000 claims description 11
- 239000003054 catalyst Substances 0.000 claims description 11
- 239000003795 chemical substances by application Substances 0.000 claims description 11
- 230000003301 hydrolyzing effect Effects 0.000 claims description 10
- 239000007787 solid Substances 0.000 claims description 8
- 229930195735 unsaturated hydrocarbon Natural products 0.000 claims description 4
- 229910052783 alkali metal Inorganic materials 0.000 claims description 3
- 239000004014 plasticizer Substances 0.000 claims description 3
- 238000004383 yellowing Methods 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 230000005670 electromagnetic radiation Effects 0.000 claims description 2
- 125000003158 alcohol group Chemical group 0.000 claims 1
- 150000004703 alkoxides Chemical class 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 description 30
- 239000000047 product Substances 0.000 description 22
- 238000006136 alcoholysis reaction Methods 0.000 description 20
- 229920005989 resin Polymers 0.000 description 18
- 239000011347 resin Substances 0.000 description 18
- 235000019441 ethanol Nutrition 0.000 description 16
- 239000011521 glass Substances 0.000 description 13
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
- 239000000843 powder Substances 0.000 description 12
- 238000010992 reflux Methods 0.000 description 12
- 238000005406 washing Methods 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 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 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 229910052708 sodium Inorganic materials 0.000 description 9
- 239000011734 sodium Substances 0.000 description 9
- 239000000155 melt Substances 0.000 description 7
- 238000003756 stirring Methods 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- 238000001035 drying Methods 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 239000000725 suspension Substances 0.000 description 5
- 150000001298 alcohols Chemical class 0.000 description 4
- 238000002845 discoloration Methods 0.000 description 4
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 4
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 230000001476 alcoholic effect Effects 0.000 description 3
- 239000005038 ethylene vinyl acetate Substances 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000005297 pyrex Substances 0.000 description 3
- 230000035484 reaction time Effects 0.000 description 3
- 230000000717 retained effect Effects 0.000 description 3
- GWHJZXXIDMPWGX-UHFFFAOYSA-N 1,2,4-trimethylbenzene Chemical compound CC1=CC=C(C)C(C)=C1 GWHJZXXIDMPWGX-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 2
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
- 230000009089 cytolysis Effects 0.000 description 2
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 239000003517 fume Substances 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000012299 nitrogen atmosphere Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 239000012429 reaction media Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 238000005029 sieve analysis Methods 0.000 description 2
- 239000007790 solid phase Substances 0.000 description 2
- 239000012798 spherical particle Substances 0.000 description 2
- 230000008961 swelling Effects 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- OKIRBHVFJGXOIS-UHFFFAOYSA-N 1,2-di(propan-2-yl)benzene Chemical compound CC(C)C1=CC=CC=C1C(C)C OKIRBHVFJGXOIS-UHFFFAOYSA-N 0.000 description 1
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000004604 Blowing Agent Substances 0.000 description 1
- 238000006418 Brown reaction Methods 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 206010042618 Surgical procedure repeated Diseases 0.000 description 1
- ACIAHEMYLLBZOI-ZZXKWVIFSA-N Unsaturated alcohol Chemical compound CC\C(CO)=C/C ACIAHEMYLLBZOI-ZZXKWVIFSA-N 0.000 description 1
- GWJZGOPLQYXBAA-UHFFFAOYSA-N [Na].CO[Na] Chemical compound [Na].CO[Na] GWJZGOPLQYXBAA-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000005233 alkylalcohol group Chemical group 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 229930007927 cymene Natural products 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000004042 decolorization Methods 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- JBSLOWBPDRZSMB-FPLPWBNLSA-N dibutyl (z)-but-2-enedioate Chemical compound CCCCOC(=O)\C=C/C(=O)OCCCC JBSLOWBPDRZSMB-FPLPWBNLSA-N 0.000 description 1
- ZEFVHSWKYCYFFL-UHFFFAOYSA-N diethyl 2-methylidenebutanedioate Chemical compound CCOC(=O)CC(=C)C(=O)OCC ZEFVHSWKYCYFFL-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- ZBGRMWIREQJHPK-UHFFFAOYSA-N ethenyl 2,2,2-trifluoroacetate Chemical compound FC(F)(F)C(=O)OC=C ZBGRMWIREQJHPK-UHFFFAOYSA-N 0.000 description 1
- YCUBDDIKWLELPD-UHFFFAOYSA-N ethenyl 2,2-dimethylpropanoate Chemical compound CC(C)(C)C(=O)OC=C YCUBDDIKWLELPD-UHFFFAOYSA-N 0.000 description 1
- MEGHWIAOTJPCHQ-UHFFFAOYSA-N ethenyl butanoate Chemical compound CCCC(=O)OC=C MEGHWIAOTJPCHQ-UHFFFAOYSA-N 0.000 description 1
- GFJVXXWOPWLRNU-UHFFFAOYSA-N ethenyl formate Chemical compound C=COC=O GFJVXXWOPWLRNU-UHFFFAOYSA-N 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- JILPJDVXYVTZDQ-UHFFFAOYSA-N lithium methoxide Chemical compound [Li+].[O-]C JILPJDVXYVTZDQ-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- HFPZCAJZSCWRBC-UHFFFAOYSA-N p-cymene Chemical compound CC(C)C1=CC=C(C)C=C1 HFPZCAJZSCWRBC-UHFFFAOYSA-N 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- SUBJHSREKVAVAR-UHFFFAOYSA-N sodium;methanol;methanolate Chemical compound [Na+].OC.[O-]C SUBJHSREKVAVAR-UHFFFAOYSA-N 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000004711 α-olefin 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
- C08F8/00—Chemical modification by after-treatment
- C08F8/12—Hydrolysis
-
- 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
- C08F2800/00—Copolymer characterised by the proportions of the comonomers expressed
- C08F2800/20—Copolymer characterised by the proportions of the comonomers expressed as weight or mass percentages
-
- 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
- C08F2810/00—Chemical modification of a polymer
- C08F2810/50—Chemical modification of a polymer wherein the polymer is a copolymer and the modification is taking place only on one or more of the monomers present in minority
Landscapes
- Chemical & Material Sciences (AREA)
- General 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)
- Treatments Of Macromolecular Shaped Articles (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US377997A US3882005A (en) | 1973-07-10 | 1973-07-10 | Process for preventing discoloration in hydrolyzed ethylene-vinyl acetate copolymers by exposure to radiation |
Publications (1)
Publication Number | Publication Date |
---|---|
NO742239L true NO742239L (it) | 1975-02-03 |
Family
ID=23491317
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO742239A NO742239L (it) | 1973-07-10 | 1974-06-19 |
Country Status (17)
Country | Link |
---|---|
US (1) | US3882005A (it) |
JP (1) | JPS5043148A (it) |
AT (1) | ATA565974A (it) |
AU (1) | AU7032674A (it) |
BE (1) | BE817504A (it) |
BR (1) | BR7405675D0 (it) |
DE (1) | DE2433188A1 (it) |
ES (1) | ES428136A1 (it) |
FI (1) | FI207174A (it) |
FR (1) | FR2236878B1 (it) |
GB (1) | GB1477386A (it) |
IT (1) | IT1015787B (it) |
NL (1) | NL7409334A (it) |
NO (1) | NO742239L (it) |
SE (1) | SE7409043L (it) |
SU (1) | SU589928A3 (it) |
ZA (1) | ZA743940B (it) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU563185B2 (en) * | 1981-05-29 | 1987-07-02 | Capsulated Systems Inc. | Hydrolyzed ethylene-vinyl ester polymers |
US4618649A (en) * | 1983-06-03 | 1986-10-21 | Minnesota Mining And Manufacturing Company | Copolymers of poly(vinyl trifluoroacetate) or poly(vinyl alcohol) |
US4694037A (en) * | 1983-06-03 | 1987-09-15 | Minnesota Mining And Manufacturing Company | Copolymers of poly(vinyl trifluoroacetate) or poly(vinyl alcohol) |
EP0363813B1 (en) * | 1988-10-06 | 1994-02-16 | Showa Denko Kabushiki Kaisha | Terpolymer and transparent laminate having excellent optical properties |
US5147702A (en) * | 1989-10-26 | 1992-09-15 | Juuro Aoyagi | Seal |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2785118A (en) * | 1954-08-30 | 1957-03-12 | Gen Aniline & Film Corp | Decolorizing solutions of polymeric nu-vinyl lactams |
US3496150A (en) * | 1968-03-22 | 1970-02-17 | Procter & Gamble | Photochemical bleaching of polymaleate homopolymers and copolymers |
FR2034002A5 (en) * | 1969-02-06 | 1970-12-04 | Du Pont | Irradiation of ethylene vinylacetatecopolymers to produce w - copolymers to produce wax additives |
GB1441986A (en) * | 1972-09-25 | 1976-07-07 | Nat Distillers Chemical Corp | Process for the accelerated alcoholysis of ehtylenevinyl ester interpolymers in the solid phase |
-
1973
- 1973-07-10 US US377997A patent/US3882005A/en not_active Expired - Lifetime
-
1974
- 1974-06-19 ZA ZA00743940A patent/ZA743940B/xx unknown
- 1974-06-19 GB GB2723874A patent/GB1477386A/en not_active Expired
- 1974-06-19 NO NO742239A patent/NO742239L/no unknown
- 1974-06-20 AU AU70326/74A patent/AU7032674A/en not_active Expired
- 1974-07-05 FI FI2071/74A patent/FI207174A/fi unknown
- 1974-07-09 AT AT565974A patent/ATA565974A/de not_active Application Discontinuation
- 1974-07-09 SE SE7409043A patent/SE7409043L/xx unknown
- 1974-07-09 SU SU742043318A patent/SU589928A3/ru active
- 1974-07-09 FR FR7423857A patent/FR2236878B1/fr not_active Expired
- 1974-07-09 IT IT24963/74A patent/IT1015787B/it active
- 1974-07-10 DE DE2433188A patent/DE2433188A1/de active Pending
- 1974-07-10 ES ES428136A patent/ES428136A1/es not_active Expired
- 1974-07-10 JP JP49078350A patent/JPS5043148A/ja active Pending
- 1974-07-10 BE BE146436A patent/BE817504A/xx unknown
- 1974-07-10 NL NL7409334A patent/NL7409334A/xx unknown
- 1974-07-10 BR BR5675/74A patent/BR7405675D0/pt unknown
Also Published As
Publication number | Publication date |
---|---|
JPS5043148A (it) | 1975-04-18 |
DE2433188A1 (de) | 1975-02-06 |
BR7405675D0 (pt) | 1975-05-20 |
SE7409043L (it) | 1975-01-13 |
FR2236878A1 (it) | 1975-02-07 |
GB1477386A (en) | 1977-06-22 |
ES428136A1 (es) | 1976-07-16 |
ZA743940B (en) | 1975-06-25 |
AU7032674A (en) | 1976-01-08 |
SU589928A3 (ru) | 1978-01-25 |
FI207174A (it) | 1975-01-11 |
US3882005A (en) | 1975-05-06 |
FR2236878B1 (it) | 1978-01-20 |
NL7409334A (nl) | 1975-01-14 |
IT1015787B (it) | 1977-05-20 |
ATA565974A (de) | 1976-12-15 |
BE817504A (fr) | 1974-11-04 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2367661A (en) | Process of photopolymerization | |
US3214492A (en) | Organic polymeric articles and prepara- tion thereof from derivatives of eth- ylene and unsaturated benzophenones | |
US3759880A (en) | Pyrrolidone-2 manufacture of insoluble and only slightly swellable poly - n - vinyl | |
US3510464A (en) | Process for the preparation of saponified homopolymers of vinyl acetate and copolymers and vinyl acetate | |
NO328079B1 (no) | Dispergeringsstabilisator for suspensjonspolymerisering av vinylforbindelse samt fremgangsmate for fremstilling av samme | |
NO742239L (it) | ||
US5625007A (en) | Process for making low optical polymers and copolymers for photoresists and optical applications | |
EP0790261B1 (en) | Process for preparing beads of polymers having an acrylic basis | |
KR20010050695A (ko) | 에틸렌-비닐 아세테이트 공중합체 수성 에멀젼의 제조방법 | |
US4003810A (en) | Preventing discoloration in hydrolyzed ethylene-vinyl acetate copolymers | |
NO178155B (no) | Fremgangsmåte for fremstilling av polymerer og kopolymerer av 4-hydroksystyren eller substituert 4-hydroksystyren med lav optisk tetthet | |
US5344901A (en) | Process for preparing acrylic polymers in suspension | |
EP3548527B1 (en) | Solution polymerization in isopropanol and water | |
CN107915806B (zh) | 一种聚丙烯颗粒接枝极性单体的方法 | |
US5300601A (en) | Suspension polymers based on methyl methacrylate | |
CA1120886A (en) | Polymerisation process | |
JPH11279210A (ja) | 低温粘度安定性の優れたポリビニルアルコールの製造方法 | |
JPS63273601A (ja) | 光重合法 | |
KR100417882B1 (ko) | 비닐아세테이트폴리머의제조방법 | |
NO116991B (it) | ||
NO153576B (no) | Vinylester/krotonsyre-kopolymer og en fremgangsmaate til fremstilling av en vinylester-kopolymer. | |
US4789716A (en) | Method of manufacturing polymaleic anhydride powders | |
US3284414A (en) | Process for preparing water-soluble copolymers of acrylic acids and n-vinyl heterocyclic monomers in a halogenated hydrocarbon | |
US3121705A (en) | Polymerization of polyvinyl acetate with an initiator of t-butyl peroxypivalate and subsequent hydrolysis to produce polyvinyl alcohol | |
WO2004035637A1 (en) | Process for making crosslinked polyvinylpyrrolidone |