ES344132A1 - Procedimiento de obtencion de copolimeros a base de clorurode vinilo. - Google Patents
Procedimiento de obtencion de copolimeros a base de clorurode vinilo.Info
- Publication number
- ES344132A1 ES344132A1 ES344132A ES344132A ES344132A1 ES 344132 A1 ES344132 A1 ES 344132A1 ES 344132 A ES344132 A ES 344132A ES 344132 A ES344132 A ES 344132A ES 344132 A1 ES344132 A1 ES 344132A1
- Authority
- ES
- Spain
- Prior art keywords
- vinyl
- methacrylate
- vinyl chloride
- fumarate
- alkyl
- 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
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 title abstract 2
- 239000000203 mixture Substances 0.000 title abstract 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 abstract 4
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 abstract 4
- 229920001577 copolymer Polymers 0.000 abstract 4
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 abstract 4
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 abstract 3
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 abstract 3
- 150000001993 dienes Chemical class 0.000 abstract 3
- 150000002148 esters Chemical class 0.000 abstract 3
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 abstract 2
- 150000001735 carboxylic acids Chemical class 0.000 abstract 2
- 239000000178 monomer Substances 0.000 abstract 2
- 150000002825 nitriles Chemical class 0.000 abstract 2
- KYPOHTVBFVELTG-OWOJBTEDSA-N (e)-but-2-enedinitrile Chemical compound N#C\C=C\C#N KYPOHTVBFVELTG-OWOJBTEDSA-N 0.000 abstract 1
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 abstract 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 abstract 1
- BXAAQNFGSQKPDZ-UHFFFAOYSA-N 3-[1,2,2-tris(prop-2-enoxy)ethoxy]prop-1-ene Chemical compound C=CCOC(OCC=C)C(OCC=C)OCC=C BXAAQNFGSQKPDZ-UHFFFAOYSA-N 0.000 abstract 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 abstract 1
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 abstract 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 abstract 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 abstract 1
- -1 alkyl vinyl ethers Chemical class 0.000 abstract 1
- 239000012736 aqueous medium Substances 0.000 abstract 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 abstract 1
- 235000013539 calcium stearate Nutrition 0.000 abstract 1
- 239000008116 calcium stearate Substances 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 abstract 1
- YCZJVRCZIPDYHH-UHFFFAOYSA-N ditridecyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCCCCCC YCZJVRCZIPDYHH-UHFFFAOYSA-N 0.000 abstract 1
- GLVVKKSPKXTQRB-UHFFFAOYSA-N ethenyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OC=C GLVVKKSPKXTQRB-UHFFFAOYSA-N 0.000 abstract 1
- AFSIMBWBBOJPJG-UHFFFAOYSA-N ethenyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC=C AFSIMBWBBOJPJG-UHFFFAOYSA-N 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-M hexadecanoate Chemical compound CCCCCCCCCCCCCCCC([O-])=O IPCSVZSSVZVIGE-UHFFFAOYSA-M 0.000 abstract 1
- YJOMWQQKPKLUBO-UHFFFAOYSA-L lead(2+);phthalate Chemical compound [Pb+2].[O-]C(=O)C1=CC=CC=C1C([O-])=O YJOMWQQKPKLUBO-UHFFFAOYSA-L 0.000 abstract 1
- 150000002763 monocarboxylic acids Chemical class 0.000 abstract 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 abstract 1
- 150000001451 organic peroxides Chemical class 0.000 abstract 1
- 230000000379 polymerizing effect Effects 0.000 abstract 1
- 229920005989 resin Polymers 0.000 abstract 1
- 239000011347 resin Substances 0.000 abstract 1
- 229920001567 vinyl ester resin Polymers 0.000 abstract 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 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
- C08F259/00—Macromolecular compounds obtained by polymerising monomers on to polymers of halogen containing monomers as defined in group C08F14/00
- C08F259/02—Macromolecular compounds obtained by polymerising monomers on to polymers of halogen containing monomers as defined in group C08F14/00 on to polymers containing chlorine
- C08F259/04—Macromolecular compounds obtained by polymerising monomers on to polymers of halogen containing monomers as defined in group C08F14/00 on to polymers containing chlorine on to polymers of vinyl chloride
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)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Graft Or Block Polymers (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR73145A FR1496772A (fr) | 1966-08-16 | 1966-08-16 | Procédé de fabrication de copolymères réticulables à base de chlorure de vinyle |
Publications (1)
Publication Number | Publication Date |
---|---|
ES344132A1 true ES344132A1 (es) | 1968-11-01 |
Family
ID=8615433
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES344132A Expired ES344132A1 (es) | 1966-08-16 | 1967-08-14 | Procedimiento de obtencion de copolimeros a base de clorurode vinilo. |
Country Status (9)
Country | Link |
---|---|
US (1) | US3544661A (es) |
AT (1) | AT277576B (es) |
BE (1) | BE702421A (es) |
CH (1) | CH475291A (es) |
ES (1) | ES344132A1 (es) |
FR (1) | FR1496772A (es) |
GB (1) | GB1138440A (es) |
NL (1) | NL6711206A (es) |
SE (1) | SE332714B (es) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3981846A (en) * | 1970-05-05 | 1976-09-21 | Dynamit Nobel Aktiengesellschaft | Workable and thermal stable interpolymers of dicarboxylic acid esters and vinyl chloride |
US4210739A (en) * | 1975-09-05 | 1980-07-01 | Stauffer Chemical Company | Internally plasticized vinyl chloride copolymer composition |
CA1116790A (en) * | 1977-01-27 | 1982-01-19 | Stauffer Chemical Company | Internally plasticized vinyl chloride copolymer |
US10138311B2 (en) | 2015-06-05 | 2018-11-27 | Lg Chem, Ltd. | Vinyl-based polymer and method of preparing the same |
EP3284761B1 (en) * | 2015-06-05 | 2020-08-05 | LG Chem, Ltd. | Vinyl chloride-based polymer and preparation method therefor |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE593821A (es) * | 1959-08-07 | |||
US3330886A (en) * | 1959-08-07 | 1967-07-11 | Pechiney Prod Chimiques Sa | Graft copolymers of polyvinyl chloride with butadiene, acrylate ester and diethylenic compound |
BE629046A (es) * | 1962-02-28 | |||
US3428707A (en) * | 1965-05-10 | 1969-02-18 | Dow Chemical Co | Modified vinyl chloride polymer compositions |
US3382215A (en) * | 1967-07-14 | 1968-05-07 | Union Carbide Corp | Virgin olefin polymers modified with organic polyisocyanates |
-
1966
- 1966-08-16 FR FR73145A patent/FR1496772A/fr not_active Expired
-
1967
- 1967-07-11 CH CH983067A patent/CH475291A/fr not_active IP Right Cessation
- 1967-08-02 GB GB35454/67A patent/GB1138440A/en not_active Expired
- 1967-08-08 BE BE702421D patent/BE702421A/xx unknown
- 1967-08-11 US US659849A patent/US3544661A/en not_active Expired - Lifetime
- 1967-08-14 ES ES344132A patent/ES344132A1/es not_active Expired
- 1967-08-15 SE SE11476/67A patent/SE332714B/xx unknown
- 1967-08-15 NL NL6711206A patent/NL6711206A/xx unknown
- 1967-08-16 AT AT753767A patent/AT277576B/de not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
CH475291A (fr) | 1969-07-15 |
FR1496772A (fr) | 1967-10-06 |
SE332714B (es) | 1971-02-15 |
GB1138440A (en) | 1969-01-01 |
AT277576B (de) | 1969-12-29 |
BE702421A (es) | 1968-02-08 |
US3544661A (en) | 1970-12-01 |
NL6711206A (es) | 1968-02-19 |
DE1745408B1 (de) | 1972-09-21 |
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