NO117391B - - Google Patents
Download PDFInfo
- Publication number
- NO117391B NO117391B NO152041A NO15204164A NO117391B NO 117391 B NO117391 B NO 117391B NO 152041 A NO152041 A NO 152041A NO 15204164 A NO15204164 A NO 15204164A NO 117391 B NO117391 B NO 117391B
- Authority
- NO
- Norway
- Prior art keywords
- trioxane
- flask
- polymerization
- polymer
- crystals
- Prior art date
Links
- BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical compound C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 claims description 54
- 238000006116 polymerization reaction Methods 0.000 claims description 24
- 239000013078 crystal Substances 0.000 claims description 23
- 238000000034 method Methods 0.000 claims description 18
- 229920001577 copolymer Polymers 0.000 claims description 12
- 238000007334 copolymerization reaction Methods 0.000 claims description 11
- 239000007788 liquid Substances 0.000 claims description 9
- 239000007858 starting material Substances 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 239000003505 polymerization initiator Substances 0.000 claims description 4
- 239000007790 solid phase Substances 0.000 claims description 4
- 230000005865 ionizing radiation Effects 0.000 claims description 3
- 239000012808 vapor phase Substances 0.000 claims 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 34
- 229920000642 polymer Polymers 0.000 description 34
- 229910052757 nitrogen Inorganic materials 0.000 description 17
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 description 12
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 12
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 12
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 230000005855 radiation Effects 0.000 description 6
- 239000007789 gas Substances 0.000 description 5
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 239000003999 initiator Substances 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- -1 polyoxymethylene chain Polymers 0.000 description 3
- 229910052573 porcelain Inorganic materials 0.000 description 3
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- VEZXCJBBBCKRPI-UHFFFAOYSA-N beta-propiolactone Chemical compound O=C1CCO1 VEZXCJBBBCKRPI-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 229960000380 propiolactone Drugs 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- VDFVNEFVBPFDSB-UHFFFAOYSA-N 1,3-dioxane Chemical compound C1COCOC1 VDFVNEFVBPFDSB-UHFFFAOYSA-N 0.000 description 1
- VDOKWPVSGXHSNP-UHFFFAOYSA-N 2-methylprop-1-en-1-one Chemical compound CC(C)=C=O VDOKWPVSGXHSNP-UHFFFAOYSA-N 0.000 description 1
- WXNZTHHGJRFXKQ-UHFFFAOYSA-N 4-chlorophenol Chemical compound OC1=CC=C(Cl)C=C1 WXNZTHHGJRFXKQ-UHFFFAOYSA-N 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- 239000011951 cationic catalyst Substances 0.000 description 1
- 238000010538 cationic polymerization reaction Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 150000002012 dioxanes Chemical class 0.000 description 1
- 150000004862 dioxolanes Chemical class 0.000 description 1
- 238000007922 dissolution test Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- CCGKOQOJPYTBIH-UHFFFAOYSA-N ethenone Chemical compound C=C=O CCGKOQOJPYTBIH-UHFFFAOYSA-N 0.000 description 1
- 238000006266 etherification reaction Methods 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000011872 intimate mixture Substances 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 150000002924 oxiranes Chemical class 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2/00—Addition polymers of aldehydes or cyclic oligomers thereof or of ketones; Addition copolymers thereof with less than 50 molar percent of other substances
- C08G2/10—Polymerisation of cyclic oligomers of formaldehyde
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2/00—Addition polymers of aldehydes or cyclic oligomers thereof or of ketones; Addition copolymers thereof with less than 50 molar percent of other substances
- C08G2/18—Copolymerisation of aldehydes or ketones
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2/00—Addition polymers of aldehydes or cyclic oligomers thereof or of ketones; Addition copolymers thereof with less than 50 molar percent of other substances
- C08G2/18—Copolymerisation of aldehydes or ketones
- C08G2/22—Copolymerisation of aldehydes or ketones with epoxy compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
- Polyethers (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE192763 | 1963-02-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO117391B true NO117391B (de) | 1969-08-04 |
Family
ID=20259078
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO152041A NO117391B (de) | 1963-02-22 | 1964-02-17 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US3442862A (de) |
| BE (1) | BE643972A (de) |
| DE (1) | DE1256897B (de) |
| DK (1) | DK109582C (de) |
| GB (3) | GB993391A (de) |
| MY (1) | MY6600094A (de) |
| NL (1) | NL6401684A (de) |
| NO (1) | NO117391B (de) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4045415A (en) * | 1972-12-23 | 1977-08-30 | Hoechst Aktiengesellschaft | Process for preparing copolymers of trioxane |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1271297A (fr) * | 1959-08-29 | 1961-09-08 | Degussa | Procédé pour préparer des polyoxyméthylènes thermiquement et chimiquement stables |
| US3156671A (en) * | 1960-03-28 | 1964-11-10 | Celanese Corp | Method for preparing trioxane-cyclic ether copolymers |
| BE610580A (fr) * | 1960-11-21 | 1962-05-21 | British Industrial Plastics | Copolymères |
| BE610364A (fr) * | 1960-12-01 | 1962-05-16 | Grace W R & Co | Perfectionnements à la production de polyoxyméthylène. |
| BE614946A (de) * | 1961-03-10 | |||
| US3297645A (en) * | 1963-10-21 | 1967-01-10 | Continental Oil Co | Polymerization of trioxane |
-
1964
- 1964-02-12 GB GB5977/64A patent/GB993391A/en not_active Expired
- 1964-02-12 GB GB5979/64A patent/GB991539A/en not_active Expired
- 1964-02-12 GB GB5978/64A patent/GB991538A/en not_active Expired
- 1964-02-14 US US344815A patent/US3442862A/en not_active Expired - Lifetime
- 1964-02-17 NO NO152041A patent/NO117391B/no unknown
- 1964-02-18 BE BE643972D patent/BE643972A/xx unknown
- 1964-02-19 DK DK80464AA patent/DK109582C/da active
- 1964-02-21 NL NL6401684A patent/NL6401684A/xx unknown
- 1964-02-21 DE DES89633A patent/DE1256897B/de active Pending
-
1966
- 1966-12-31 MY MY196694A patent/MY6600094A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| GB991539A (en) | 1965-05-12 |
| BE643972A (de) | 1964-06-15 |
| DE1256897B (de) | 1967-12-21 |
| DK109582C (da) | 1968-05-13 |
| MY6600094A (en) | 1966-12-31 |
| NL6401684A (de) | 1964-08-24 |
| GB993391A (en) | 1965-05-26 |
| GB991538A (en) | 1965-05-12 |
| US3442862A (en) | 1969-05-06 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US2921006A (en) | Polymerization with high energy electrons | |
| Yuki et al. | Stereospecific polymerization of benzyl vinyl ether by BF3· OEt2 | |
| KR100264106B1 (ko) | 생분해성 탄성체의 제조방법 | |
| NO117391B (de) | ||
| Goodman et al. | Stereochemistry of Poly-α-methylvinyl Methyl Ether | |
| Voyer et al. | Synthesis and polymerization of racemic and optically active β‐substituted β‐propiolactones. III. β‐monosubstituted monomers and polymers | |
| Millan et al. | Relation between thermal degradation and tacticity of PVC | |
| US3433724A (en) | Grafting of acrylonitrile and styrene onto polyvinyl chloride using high energy radiation | |
| Ishigaki et al. | Radiation‐induced postpolymerization of trioxane in the solid state. II. Kinetic study of radiation‐induced postpolymerization of trioxane in dry and high‐vacuum system | |
| Miyata et al. | Functional monomers and polymers. XXXVIII. Postirradiation polymerization of 2, 3‐dimethylbutadiene in deoxycholic acid canal complexes | |
| Martinez et al. | Specific polymer-solvent interaction and stereospecificity of nucleophilic substitution reaction of PVC | |
| US3366561A (en) | Ionizing irradiation polymerization of trioxane with copolymerizable stabilizing comonomers | |
| Bamford et al. | The polymerization of crystalline methacrylic acid initiated by ultra-violet radiation I—Radical conformations and reaction mechanism | |
| US3616368A (en) | Method for the radiation polymerization of polyoxymethylene | |
| US4356071A (en) | Thermally stable polyoxymethylene containing polymers | |
| US3305464A (en) | Polymerization of trioxane | |
| Usanmaz et al. | Crystal structure effect on solid state polymerization of allylurea | |
| Chawla et al. | Solid‐state polymerization of hexamethylcyclotrisiloxane. II | |
| US3516973A (en) | Process for the polymerization of beta-lactones | |
| US3165482A (en) | Polymers from n-hetero-bicyclo alkanes and process for producing same | |
| Barkalov et al. | Post‐irradiation grafting of tetrafluoroethylene at low temperatures | |
| Kumar et al. | Simulation of cyclics and degradation product formation in polyethylene terephthalate reactors | |
| SU602509A1 (ru) | Привитые сополимеры поливинилбутирал с винилфторидом | |
| Miao et al. | Modification of poly (D, L-lactic acid)-co-poly (ethylene glycol) copolymer by low energy electron beam (EB) radiation | |
| US3830715A (en) | Process for the preparation of oxymethylene polymers in the presence of an acyclic acetal and a cyclic acetal |