IL25163A - Process for making polyoxymethylene copolymers - Google Patents
Process for making polyoxymethylene copolymersInfo
- Publication number
- IL25163A IL25163A IL25163A IL2516366A IL25163A IL 25163 A IL25163 A IL 25163A IL 25163 A IL25163 A IL 25163A IL 2516366 A IL2516366 A IL 2516366A IL 25163 A IL25163 A IL 25163A
- Authority
- IL
- Israel
- Prior art keywords
- formal
- alkyl
- glycidyl
- weight
- trioxane
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 5
- 229920012196 Polyoxymethylene Copolymer Polymers 0.000 title description 2
- 229920001577 copolymer Polymers 0.000 claims description 14
- 150000001875 compounds Chemical class 0.000 claims description 13
- 150000004292 cyclic ethers Chemical class 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 7
- 239000003054 catalyst Substances 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 5
- 230000001588 bifunctional effect Effects 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 230000000379 polymerizing effect Effects 0.000 claims description 4
- 125000005704 oxymethylene group Chemical group [H]C([H])([*:2])O[*:1] 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 2
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 2
- BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical compound C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 claims 4
- 125000001570 methylene group Chemical class [H]C([H])([*:1])[*:2] 0.000 claims 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- KQBSGRWMSNFIPG-UHFFFAOYSA-N trioxane Chemical compound C1COOOC1 KQBSGRWMSNFIPG-UHFFFAOYSA-N 0.000 description 10
- 229920000642 polymer Polymers 0.000 description 9
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 6
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 6
- 238000006116 polymerization reaction Methods 0.000 description 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 5
- 238000001746 injection moulding Methods 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 229920001897 terpolymer Polymers 0.000 description 4
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 235000011114 ammonium hydroxide Nutrition 0.000 description 3
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical class FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 3
- 230000007062 hydrolysis Effects 0.000 description 3
- 238000006460 hydrolysis reaction Methods 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- HPILSDOMLLYBQF-UHFFFAOYSA-N 2-[1-(oxiran-2-ylmethoxy)butoxymethyl]oxirane Chemical compound C1OC1COC(CCC)OCC1CO1 HPILSDOMLLYBQF-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 150000004982 aromatic amines Chemical class 0.000 description 2
- 235000019445 benzyl alcohol Nutrition 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- AUAGGMPIKOZAJZ-UHFFFAOYSA-N 1,3,6-trioxocane Chemical compound C1COCOCCO1 AUAGGMPIKOZAJZ-UHFFFAOYSA-N 0.000 description 1
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 1
- IUDNGVFSUHFMCF-UHFFFAOYSA-N 4-(chloromethyl)-1,3-dioxolane Chemical compound ClCC1COCO1 IUDNGVFSUHFMCF-UHFFFAOYSA-N 0.000 description 1
- ICMFHHGKLRTCBM-UHFFFAOYSA-N 4-nitrobenzenediazonium Chemical compound [O-][N+](=O)C1=CC=C([N+]#N)C=C1 ICMFHHGKLRTCBM-UHFFFAOYSA-N 0.000 description 1
- 229910015900 BF3 Inorganic materials 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- -1 aliphatic amines Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001409 amidines Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000011951 cationic catalyst Substances 0.000 description 1
- 101150084500 cel2 gene Proteins 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000012954 diazonium Substances 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-O diazynium Chemical compound [NH+]#N IJGRMHOSHXDMSA-UHFFFAOYSA-O 0.000 description 1
- 230000005518 electrochemistry Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- C08G2/06—Catalysts
-
- 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
-
- 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
- C08G2/24—Copolymerisation of aldehydes or ketones with acetals
-
- 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
- C08G4/00—Condensation polymers of aldehydes or ketones with polyalcohols; Addition polymers of heterocyclic oxygen compounds containing in the ring at least once the grouping —O—C—O—
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)
- Compositions Of Macromolecular Compounds (AREA)
- Debarking, Splitting, And Disintegration Of Timber (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF45425A DE1301096B (de) | 1965-03-05 | 1965-03-05 | Verfahren zur Herstellung von Copolymerisaten des Trioxans |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| IL25163A true IL25163A (en) | 1970-04-20 |
Family
ID=7100488
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL25163A IL25163A (en) | 1965-03-05 | 1966-02-11 | Process for making polyoxymethylene copolymers |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US3453238A (en, 2012) |
| JP (1) | JPS4326871B1 (en, 2012) |
| AT (1) | AT255763B (en, 2012) |
| BE (1) | BE677436A (en, 2012) |
| CH (1) | CH468421A (en, 2012) |
| DE (1) | DE1301096B (en, 2012) |
| ES (1) | ES323739A1 (en, 2012) |
| FR (1) | FR1470692A (en, 2012) |
| GB (1) | GB1105858A (en, 2012) |
| IL (1) | IL25163A (en, 2012) |
| NL (1) | NL143961B (en, 2012) |
| NO (1) | NO117658B (en, 2012) |
| SE (1) | SE318411B (en, 2012) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH315369D (en, 2012) * | 1968-03-05 | 1900-01-01 | ||
| TWI237035B (en) * | 1998-07-24 | 2005-08-01 | Polyplastics Co | Polyacetal copolymer |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1114325B (de) * | 1958-04-03 | 1961-09-28 | Bayer Ag | Verfahren zur Herstellung von hochmolekularen Polyadditionsprodukten |
| GB971915A (en) * | 1960-11-09 | 1964-10-07 | Celanese Corp | Mouldable oxymethylene polymers |
| BE634303A (en, 2012) * | 1962-06-28 | |||
| DE1303485C2 (de) * | 1962-11-30 | 1979-07-19 | Hoechst Ag, 6000 Frankfurt | Verfahren zur herstellung von copolymerisaten des trioxans |
| FR1376169A (fr) * | 1962-11-30 | 1964-10-23 | Hoechst Ag | Procédé de préparation de copolymères à base de trioxanne |
| US3275604A (en) * | 1963-07-19 | 1966-09-27 | Celanese Corp | Moldable oxymethylene copolymers and method of preparing same |
-
1965
- 1965-03-05 DE DEF45425A patent/DE1301096B/de active Pending
-
1966
- 1966-02-10 US US526399A patent/US3453238A/en not_active Expired - Lifetime
- 1966-02-11 IL IL25163A patent/IL25163A/en unknown
- 1966-02-22 GB GB7693/66A patent/GB1105858A/en not_active Expired
- 1966-02-23 NL NL666602331A patent/NL143961B/xx unknown
- 1966-03-02 SE SE2758/66A patent/SE318411B/xx unknown
- 1966-03-02 ES ES0323739A patent/ES323739A1/es not_active Expired
- 1966-03-02 CH CH295866A patent/CH468421A/de unknown
- 1966-03-03 AT AT200166A patent/AT255763B/de active
- 1966-03-04 JP JP1292266A patent/JPS4326871B1/ja active Pending
- 1966-03-04 FR FR52082A patent/FR1470692A/fr not_active Expired
- 1966-03-04 NO NO161961A patent/NO117658B/no unknown
- 1966-03-07 BE BE677436D patent/BE677436A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AT255763B (de) | 1967-07-25 |
| FR1470692A (fr) | 1967-02-24 |
| CH468421A (de) | 1969-02-15 |
| NL143961B (nl) | 1974-11-15 |
| NO117658B (en, 2012) | 1969-09-08 |
| DE1301096B (de) | 1969-08-14 |
| JPS4326871B1 (en, 2012) | 1968-11-19 |
| US3453238A (en) | 1969-07-01 |
| ES323739A1 (es) | 1967-01-16 |
| NL6602331A (en, 2012) | 1966-09-06 |
| SE318411B (en, 2012) | 1969-12-08 |
| BE677436A (en, 2012) | 1966-09-07 |
| GB1105858A (en) | 1968-03-13 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US5608030A (en) | Process for the preparation of polyacetals | |
| US3256246A (en) | Copolymerization of trioxane with preformed linear polymers | |
| EP0325052B1 (en) | Process for the preparation of acetal polymer or copolymer | |
| US3385827A (en) | Trioxane terpolymers | |
| US3306877A (en) | Process for the manufacture of copolyacetals | |
| US3519696A (en) | Process for preparing copolymers of trioxane | |
| US4931535A (en) | Process for the preparation of acetal polymer or copolymer | |
| US3297647A (en) | Product and process for the manufacture of linear terpolymers of acetals | |
| IL25163A (en) | Process for making polyoxymethylene copolymers | |
| US3457229A (en) | Copolymers of trioxane,cyclic ethers and trifunctional compounds and process for their manufacture | |
| JP2011516702A (ja) | オキシメチレンコポリマー及びその使用並びにオキシメチレンコポリマーの製造方法 | |
| US3457228A (en) | Polymerization of trioxane with polyacetals | |
| USRE39182E1 (en) | Process for the preparation of thermally stable polyoxymethylene copolymers | |
| US3424725A (en) | Copolymers of trioxane,cyclic ethers,and bifunctional epoxides and a process for their manufacture | |
| US3494893A (en) | Process for preparing copolymers of trioxane | |
| US3453239A (en) | Process for the manufacture of copolymers of trioxane and cyclic ethers with dioxolanyl - 4 - methyl-alkyl formals | |
| KR100306072B1 (ko) | 중합 반응의 정지 방법 | |
| US3687898A (en) | Process for the production of heat resistant oxymethylene polymer | |
| US4151346A (en) | Process for preparing oxymethylene polymers in a granular form | |
| US4082729A (en) | Process for the preparation of oxymethylene polymers | |
| US3435006A (en) | Copolyacetals and process for their manufacture | |
| US3477992A (en) | Polyoxymethylene copolymers | |
| US3598788A (en) | Process for the manufacture of copolymers of trioxane | |
| Price et al. | The polymerization and copolymerization of trioxane | |
| US3557058A (en) | Process for obtaining polyoxymethylenes having controlled molecular weight and products obtained therefrom |