DE877062C - Verfahren zur Herstellung eines polymeren Acetals - Google Patents
Verfahren zur Herstellung eines polymeren AcetalsInfo
- Publication number
- DE877062C DE877062C DEP4691D DEP0004691D DE877062C DE 877062 C DE877062 C DE 877062C DE P4691 D DEP4691 D DE P4691D DE P0004691 D DEP0004691 D DE P0004691D DE 877062 C DE877062 C DE 877062C
- Authority
- DE
- Germany
- Prior art keywords
- production
- acetal
- polymeric acetal
- polymerization
- viscous
- 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
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 title claims description 9
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 title claims description 9
- 238000004519 manufacturing process Methods 0.000 title claims description 4
- 238000000034 method Methods 0.000 title claims description 4
- 238000006116 polymerization reaction Methods 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims description 3
- 239000002685 polymerization catalyst Substances 0.000 claims description 2
- 239000000853 adhesive Substances 0.000 description 6
- 230000001070 adhesive effect Effects 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 4
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- FFRBMBIXVSCUFS-UHFFFAOYSA-N 2,4-dinitro-1-naphthol Chemical compound C1=CC=C2C(O)=C([N+]([O-])=O)C=C([N+]([O-])=O)C2=C1 FFRBMBIXVSCUFS-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 229910021627 Tin(IV) chloride Inorganic materials 0.000 description 2
- 239000002998 adhesive polymer Substances 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 2
- 239000004922 lacquer Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000001226 reprecipitation Methods 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- APLNAFMUEHKRLM-UHFFFAOYSA-N 2-[5-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-1,3,4-oxadiazol-2-yl]-1-(3,4,6,7-tetrahydroimidazo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1=NN=C(O1)CC(=O)N1CC2=C(CC1)N=CN2 APLNAFMUEHKRLM-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical class CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- OSKNUZYLXFBIHL-UHFFFAOYSA-N azanium;hydron;phthalate Chemical compound N.OC(=O)C1=CC=CC=C1C(O)=O OSKNUZYLXFBIHL-UHFFFAOYSA-N 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229940068911 chloride hexahydrate Drugs 0.000 description 1
- 238000005352 clarification Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- NIQQIJXGUZVEBB-UHFFFAOYSA-N methanol;propan-2-one Chemical compound OC.CC(C)=O NIQQIJXGUZVEBB-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 229920001289 polyvinyl ether Polymers 0.000 description 1
- LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229910002007 uranyl nitrate Inorganic materials 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- 239000011592 zinc chloride 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
- C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
Landscapes
- 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)
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL64618D NL64618C (enrdf_load_stackoverflow) | 1943-10-26 | ||
| DEP4691D DE877062C (de) | 1943-10-26 | 1943-10-26 | Verfahren zur Herstellung eines polymeren Acetals |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEP4691D DE877062C (de) | 1943-10-26 | 1943-10-26 | Verfahren zur Herstellung eines polymeren Acetals |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE877062C true DE877062C (de) | 1953-05-21 |
Family
ID=7359585
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEP4691D Expired DE877062C (de) | 1943-10-26 | 1943-10-26 | Verfahren zur Herstellung eines polymeren Acetals |
Country Status (2)
| Country | Link |
|---|---|
| DE (1) | DE877062C (enrdf_load_stackoverflow) |
| NL (1) | NL64618C (enrdf_load_stackoverflow) |
-
0
- NL NL64618D patent/NL64618C/xx active
-
1943
- 1943-10-26 DE DEP4691D patent/DE877062C/de not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| NL64618C (enrdf_load_stackoverflow) |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE870032C (de) | Verfahren zur Herstellung von harzartigen Kondensationsprodukten | |
| DE877062C (de) | Verfahren zur Herstellung eines polymeren Acetals | |
| DE1097138B (de) | Verfahren zur Herstellung von Polymeren und Mischpolymeren | |
| DE1062012B (de) | Verfahren zur Herstellung von Polymerisaten des Acroleins | |
| DE1113572B (de) | Verfahren zur Herstellung von hydroxylgruppenhaltigen Mischpoly-merisaten aus Vinylchlorid und Vinylacetat | |
| DE888769C (de) | Verfahren zur Herstellung von Kunststoffen | |
| DE446562C (de) | Verfahren zur Herstellung von in Benzol, Spiritus u. dgl. loeslichen Polymerisationsprodukten des Vinylacetats und deren Lacken | |
| DE1770580A1 (de) | Verfahren zur Herstellung modifizierter Polyvinylalkohole | |
| DE882091C (de) | Verfahren zur Durchfuehrung organischer katalytischer Reaktionen | |
| DE583914C (de) | Verfahren zur Herstellung kautschuk- oder harzartiger Massen | |
| DE827553C (de) | Verfahren zur Herstellung von Kunststoffen | |
| DE695561C (de) | Verfahren zur Darstellung von loeslichen und zugleich hochmolekularen Polymerisationsprodukten von Acrylsaeureverbindungen | |
| DE576141C (de) | Verfahren zur Polymerisation von ungesaettigten Verbindungen | |
| DE960813C (de) | Verfahren zur Herstellung von ungesaettigten ª†- und ª€-Laktonen | |
| DE972529C (de) | Verfahren zur Herstellung von lagerbestaendigen, in der Hitze haertbaren Methyl- oder AEthylsilikonen | |
| DE707280C (de) | Verfahren zur Herstellung von Polymerisationsprodukten der Derivate von olefinischen Oxoverbindungen | |
| DE604776C (de) | Verfahren zur Darstellung von Polyvinylestern | |
| DE875569C (de) | Verfahren zur Herstellung von harzartigen Produkten | |
| DE858549C (de) | Verfahren zur Herstellung von neuen Celluloseabkoemmlingen | |
| EP0004405B1 (de) | Verfahren zur Herstellung von hochreinem Tetrahydrophthalsäureanhydrid | |
| DE963556C (de) | Verfahren zur Herstellung von haertbaren Furfurylalkoholharzen | |
| DE961131C (de) | Verfahren zur Polymerisation von Vinylverbindungen | |
| CH457426A (de) | Verwendung von Verbindungen als UV-Absorber für nicht-textile organische Materialien | |
| DE712277C (de) | Verfahren zur Herstellung polymerer Verbindungen | |
| DE952894C (de) | Verfahren zur Herstellung von AEthern des 2-Methylolbuten-1-ons-(3) |