CA1089595A - Polymerization process using diperoxy ketals as finishing catalysts - Google Patents
Polymerization process using diperoxy ketals as finishing catalystsInfo
- Publication number
- CA1089595A CA1089595A CA290,695A CA290695A CA1089595A CA 1089595 A CA1089595 A CA 1089595A CA 290695 A CA290695 A CA 290695A CA 1089595 A CA1089595 A CA 1089595A
- Authority
- CA
- Canada
- Prior art keywords
- carbons
- groups
- bis
- initiator
- hydrocarbyl
- 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
- 238000006116 polymerization reaction Methods 0.000 title claims abstract 7
- 239000003054 catalyst Substances 0.000 title claims description 5
- 239000000178 monomer Substances 0.000 claims abstract description 31
- 238000000034 method Methods 0.000 claims abstract description 21
- 239000003999 initiator Substances 0.000 claims abstract 12
- 125000001183 hydrocarbyl group Chemical group 0.000 claims abstract 7
- 229920002554 vinyl polymer Polymers 0.000 claims abstract 5
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims abstract 3
- 238000010526 radical polymerization reaction Methods 0.000 claims abstract 2
- -1 t-amylperoxy Chemical group 0.000 claims description 8
- 229920000642 polymer Polymers 0.000 claims description 5
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 claims description 4
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 2
- RIPYNJLMMFGZSX-UHFFFAOYSA-N (5-benzoylperoxy-2,5-dimethylhexan-2-yl) benzenecarboperoxoate Chemical compound C=1C=CC=CC=1C(=O)OOC(C)(C)CCC(C)(C)OOC(=O)C1=CC=CC=C1 RIPYNJLMMFGZSX-UHFFFAOYSA-N 0.000 claims 2
- HARQWLDROVMFJE-UHFFFAOYSA-N ethyl 3,3-bis(tert-butylperoxy)butanoate Chemical compound CCOC(=O)CC(C)(OOC(C)(C)C)OOC(C)(C)C HARQWLDROVMFJE-UHFFFAOYSA-N 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- JUIBLDFFVYKUAC-UHFFFAOYSA-N [5-(2-ethylhexanoylperoxy)-2,5-dimethylhexan-2-yl] 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOC(C)(C)CCC(C)(C)OOC(=O)C(CC)CCCC JUIBLDFFVYKUAC-UHFFFAOYSA-N 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 125000003302 alkenyloxy group Chemical group 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000003710 aryl alkyl group Chemical group 0.000 claims 1
- 125000004104 aryloxy group Chemical group 0.000 claims 1
- BXIQXYOPGBXIEM-UHFFFAOYSA-N butyl 4,4-bis(tert-butylperoxy)pentanoate Chemical compound CCCCOC(=O)CCC(C)(OOC(C)(C)C)OOC(C)(C)C BXIQXYOPGBXIEM-UHFFFAOYSA-N 0.000 claims 1
- 125000000000 cycloalkoxy group Chemical group 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- QKHUFWBDCOLHNW-UHFFFAOYSA-N ditert-butyl 2-nonyldecanediperoxoate Chemical compound CCCCCCCCCC(C(=O)OOC(C)(C)C)CCCCCCCC(=O)OOC(C)(C)C QKHUFWBDCOLHNW-UHFFFAOYSA-N 0.000 claims 1
- YKYONYBAUNKHLG-UHFFFAOYSA-N n-Propyl acetate Natural products CCCOC(C)=O YKYONYBAUNKHLG-UHFFFAOYSA-N 0.000 claims 1
- 230000000379 polymerizing effect Effects 0.000 claims 1
- 229940090181 propyl acetate Drugs 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 22
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 14
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 12
- 125000000864 peroxy group Chemical group O(O*)* 0.000 description 11
- 102100024133 Coiled-coil domain-containing protein 50 Human genes 0.000 description 10
- 101000910772 Homo sapiens Coiled-coil domain-containing protein 50 Proteins 0.000 description 10
- WCVOGSZTONGSQY-UHFFFAOYSA-N 2,4,6-trichloroanisole Chemical compound COC1=C(Cl)C=C(Cl)C=C1Cl WCVOGSZTONGSQY-UHFFFAOYSA-N 0.000 description 5
- 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 description 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 4
- 229920008712 Copo Polymers 0.000 description 3
- 101150083807 HSD17B10 gene Proteins 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 239000012969 di-tertiary-butyl peroxide Substances 0.000 description 2
- MYWUZJCMWCOHBA-VIFPVBQESA-N methamphetamine Chemical compound CN[C@@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-VIFPVBQESA-N 0.000 description 2
- 239000001294 propane Substances 0.000 description 2
- GOAHRBQLKIZLKG-UHFFFAOYSA-N 1-tert-butylperoxybutane Chemical compound CCCCOOC(C)(C)C GOAHRBQLKIZLKG-UHFFFAOYSA-N 0.000 description 1
- CWPKTBMRVATCBL-UHFFFAOYSA-N 3-[1-[1-[(2-methylphenyl)methyl]piperidin-4-yl]piperidin-4-yl]-1h-benzimidazol-2-one Chemical compound CC1=CC=CC=C1CN1CCC(N2CCC(CC2)N2C(NC3=CC=CC=C32)=O)CC1 CWPKTBMRVATCBL-UHFFFAOYSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- XUKUURHRXDUEBC-KAYWLYCHSA-N Atorvastatin Chemical compound C=1C=CC=CC=1C1=C(C=2C=CC(F)=CC=2)N(CC[C@@H](O)C[C@@H](O)CC(O)=O)C(C(C)C)=C1C(=O)NC1=CC=CC=C1 XUKUURHRXDUEBC-KAYWLYCHSA-N 0.000 description 1
- 101100087530 Caenorhabditis elegans rom-1 gene Proteins 0.000 description 1
- 206010007134 Candida infections Diseases 0.000 description 1
- 241000905957 Channa melasoma Species 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 101100424709 Danio rerio tbxta gene Proteins 0.000 description 1
- 101100536354 Drosophila melanogaster tant gene Proteins 0.000 description 1
- 239000004243 E-number Substances 0.000 description 1
- 235000019227 E-number Nutrition 0.000 description 1
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 1
- 101100305983 Mus musculus Rom1 gene Proteins 0.000 description 1
- 241001163743 Perlodes Species 0.000 description 1
- 240000001987 Pyrus communis Species 0.000 description 1
- 102100022563 Tubulin polymerization-promoting protein Human genes 0.000 description 1
- 101710158555 Tubulin polymerization-promoting protein Proteins 0.000 description 1
- 125000005605 benzo group Chemical group 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 229940097156 peroxyl Drugs 0.000 description 1
- 239000005297 pyrex Substances 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- SYOKIDBDQMKNDQ-XWTIBIIYSA-N vildagliptin Chemical compound C1C(O)(C2)CC(C3)CC1CC32NCC(=O)N1CCC[C@H]1C#N SYOKIDBDQMKNDQ-XWTIBIIYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- CZPRKINNVBONSF-UHFFFAOYSA-M zinc;dioxido(oxo)phosphanium Chemical compound [Zn+2].[O-][P+]([O-])=O CZPRKINNVBONSF-UHFFFAOYSA-M 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
- C08F4/00—Polymerisation catalysts
- C08F4/28—Oxygen or compounds releasing free oxygen
- C08F4/32—Organic compounds
- C08F4/38—Mixtures of peroxy-compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polymerization Catalysts (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US757,189 | 1977-01-06 | ||
| US05/757,189 US4130700A (en) | 1977-01-06 | 1977-01-06 | Polymerization process using diperoxy ketals as finishing catalysts |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1089595A true CA1089595A (en) | 1980-11-11 |
Family
ID=25046771
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA290,695A Expired CA1089595A (en) | 1977-01-06 | 1977-11-10 | Polymerization process using diperoxy ketals as finishing catalysts |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US4130700A (enExample) |
| JP (1) | JPS5385876A (enExample) |
| CA (1) | CA1089595A (enExample) |
| DE (1) | DE2756035A1 (enExample) |
| FR (1) | FR2376872A1 (enExample) |
| GB (1) | GB1588878A (enExample) |
| IT (1) | IT1092246B (enExample) |
| NL (1) | NL184421B (enExample) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS56167706A (en) * | 1980-05-30 | 1981-12-23 | Denki Kagaku Kogyo Kk | Polymerization of styrene type monomer |
| US4330495A (en) * | 1981-02-23 | 1982-05-18 | U.S. Peroxygen Company | Novel method of crosslinking/foaming of low density polyethylene using linear peroxyketals |
| US4804775A (en) * | 1986-09-09 | 1989-02-14 | Pennwalt Corporation | Process for reducing residual monomers in low viscosity polymer-polyols |
| DE4038625A1 (de) * | 1990-12-04 | 1992-06-11 | Basf Ag | Substanz- und suspensionspolymerisate auf der basis von methylmethacrylat |
| CA2063473C (en) * | 1991-07-01 | 1998-09-22 | T. Hwee Ng | Process for preparing copolymers |
| US5637646A (en) * | 1995-12-14 | 1997-06-10 | Minnesota Mining And Manufacturing Company | Bulk radical polymerization using a batch reactor |
| DE19749570A1 (de) * | 1997-11-10 | 1999-05-12 | Basf Ag | Verfahren zur Herstellung von expandierbaren Styrolpolymerisaten |
| JP4011415B2 (ja) * | 2002-06-20 | 2007-11-21 | 日本ペイント株式会社 | アクリル共重合体の製造方法 |
| US7605216B2 (en) * | 2004-11-10 | 2009-10-20 | Basf Corporation | Method of reducing a content of a residual styrene monomer in a polyol |
| KR20100090287A (ko) * | 2007-11-20 | 2010-08-13 | 아크조 노벨 엔.브이. | 스티렌계 （코）폴리머의 제조 방법 |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA751552A (en) * | 1967-01-24 | B. Towne Edmund | Process for polymerizing unsaturated polymerizable compounds | |
| CA915850A (en) * | 1972-11-28 | Rexall Drug And Chemical Company | Process for the polymerization of a vinyl aromatic compound | |
| NL235733A (enExample) * | 1958-02-03 | |||
| NL120227C (enExample) * | 1962-10-12 | 1965-03-15 | ||
| DE1234989C2 (de) * | 1962-12-14 | 1973-10-04 | Eastman Kodak Co | Verfahren zur Herstellung von Polymerisaten aus aethylenisch ungesaettigten Verbindungen |
| US3287337A (en) * | 1962-12-14 | 1966-11-22 | Eastman Kodak Co | Esters of diperoxy carbonic acid and polymerization processes employing the same |
| US3414547A (en) * | 1963-06-13 | 1968-12-03 | Nalco Chemical Co | Polymerization process |
| DE1443912C3 (de) * | 1964-12-08 | 1975-07-10 | Bayer Ag, 5090 Leverkusen | 3,5-Dialkyl-4-hydroxy-benzylamide der Acryl- bzw. Methacrylsäure und Verfahren zu ihrer Herstellung |
| GB1243197A (en) * | 1968-01-18 | 1971-08-18 | British Petroleum Co | Polymerisation process |
| US3839390A (en) * | 1968-07-17 | 1974-10-01 | Pennwalt Corp | Polyperoxides affording sequential free radical generation |
| US3534009A (en) * | 1969-01-29 | 1970-10-13 | Du Pont | Method for reducing residual vinyl acetate monomer |
| US3832336A (en) * | 1970-06-03 | 1974-08-27 | Pennwalt Corp | Curing and polymerizing processes employing beta-substituted diperoxyketals |
| US3763275A (en) * | 1970-06-03 | 1973-10-02 | Pennwalt Corp | Curing processes employing beta-substituted diperoxyketals |
| JPS5220473B1 (enExample) * | 1970-06-29 | 1977-06-03 | ||
| US3784532A (en) * | 1970-09-18 | 1974-01-08 | Rohm & Haas | Bulk polymerization process modified with solvent to reduce residual monomer content |
| GB1330896A (en) * | 1970-11-06 | 1973-09-19 | Monsanto Chemicals | Polymerisation process |
| GB1329859A (en) * | 1970-11-06 | 1973-09-12 | Monsanto Chemicals | Polymerisation process |
| US3681305A (en) * | 1970-11-13 | 1972-08-01 | Richardson Co | Transparent,high heat polystyrenes |
| US3743630A (en) * | 1971-06-30 | 1973-07-03 | Argus Chem | Styrene polymerization with ring substituted alkyl perbenzoates and new branched chain alkyl perbenzoates |
| BE789896A (nl) * | 1971-11-01 | 1973-02-01 | Akzo Nv | Werkwijze voor het uitvoeren van door organische peroxyden geinitieerdechemische reacties |
| US3960994A (en) * | 1974-11-26 | 1976-06-01 | The United States Of America As Represented By The United States Energy Research And Development Administration | Preparation of high temperature gas-cooled reactor fuel element |
-
1977
- 1977-01-06 US US05/757,189 patent/US4130700A/en not_active Expired - Lifetime
- 1977-11-10 CA CA290,695A patent/CA1089595A/en not_active Expired
- 1977-11-24 GB GB48999/77A patent/GB1588878A/en not_active Expired
- 1977-12-02 NL NLAANVRAGE7713366,A patent/NL184421B/xx not_active Application Discontinuation
- 1977-12-15 FR FR7737845A patent/FR2376872A1/fr active Granted
- 1977-12-15 DE DE19772756035 patent/DE2756035A1/de active Granted
- 1977-12-21 IT IT52325/77A patent/IT1092246B/it active
-
1978
- 1978-01-05 JP JP5478A patent/JPS5385876A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| IT1092246B (it) | 1985-07-06 |
| US4130700A (en) | 1978-12-19 |
| GB1588878A (en) | 1981-04-29 |
| DE2756035A1 (de) | 1978-07-13 |
| JPS6160083B2 (enExample) | 1986-12-19 |
| JPS5385876A (en) | 1978-07-28 |
| NL184421B (nl) | 1989-02-16 |
| NL7713366A (nl) | 1978-07-10 |
| FR2376872A1 (fr) | 1978-08-04 |
| FR2376872B1 (enExample) | 1981-02-13 |
| DE2756035C2 (enExample) | 1988-06-09 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MKEX | Expiry |