DE1235281B - Verfahren zur Herstellung von Hartwachsen - Google Patents
Verfahren zur Herstellung von HartwachsenInfo
- Publication number
- DE1235281B DE1235281B DEF46581A DEF0046581A DE1235281B DE 1235281 B DE1235281 B DE 1235281B DE F46581 A DEF46581 A DE F46581A DE F0046581 A DEF0046581 A DE F0046581A DE 1235281 B DE1235281 B DE 1235281B
- Authority
- DE
- Germany
- Prior art keywords
- polymerization
- production
- waxes
- hard waxes
- hard
- 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.)
- Pending
Links
- 239000001993 wax Substances 0.000 title claims description 19
- 238000000034 method Methods 0.000 title claims description 12
- 238000004519 manufacturing process Methods 0.000 title claims description 5
- 238000006116 polymerization reaction Methods 0.000 claims description 15
- 239000003054 catalyst Substances 0.000 claims description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- -1 glycidyl ether aliphatic alcohols Chemical class 0.000 claims description 3
- 238000005727 Friedel-Crafts reaction Methods 0.000 claims description 2
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 8
- 239000000203 mixture Substances 0.000 description 6
- 239000000460 chlorine Substances 0.000 description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 229910052801 chlorine Inorganic materials 0.000 description 4
- 150000002170 ethers Chemical class 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 239000004593 Epoxy Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 229910015900 BF3 Inorganic materials 0.000 description 2
- 239000001293 FEMA 3089 Substances 0.000 description 2
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
- NOPFSRXAKWQILS-UHFFFAOYSA-N docosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCO NOPFSRXAKWQILS-UHFFFAOYSA-N 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical class O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- YZUMRMCHAJVDRT-UHFFFAOYSA-N 2-(hexadecoxymethyl)oxirane Chemical compound CCCCCCCCCCCCCCCCOCC1CO1 YZUMRMCHAJVDRT-UHFFFAOYSA-N 0.000 description 1
- ZXJBWUAALADCRI-UHFFFAOYSA-N 2-(octadecoxymethyl)oxirane Chemical compound CCCCCCCCCCCCCCCCCCOCC1CO1 ZXJBWUAALADCRI-UHFFFAOYSA-N 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 241000220317 Rosa Species 0.000 description 1
- 229910021627 Tin(IV) chloride Inorganic materials 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- VMPVEPPRYRXYNP-UHFFFAOYSA-I antimony(5+);pentachloride Chemical compound Cl[Sb](Cl)(Cl)(Cl)Cl VMPVEPPRYRXYNP-UHFFFAOYSA-I 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- XENVCRGQTABGKY-ZHACJKMWSA-N chlorohydrin Chemical compound CC#CC#CC#CC#C\C=C\C(Cl)CO XENVCRGQTABGKY-ZHACJKMWSA-N 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000012459 cleaning agent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000007033 dehydrochlorination reaction Methods 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 229960000735 docosanol Drugs 0.000 description 1
- 150000002118 epoxides Chemical class 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- BXWNKGSJHAJOGX-UHFFFAOYSA-N n-hexadecyl alcohol Natural products CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 1
- GLDOVTGHNKAZLK-UHFFFAOYSA-N n-octadecyl alcohol Natural products CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001289 polyvinyl ether Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/04—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers only
- C08G65/22—Cyclic ethers having at least one atom other than carbon and hydrogen outside the ring
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyethers (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF46581A DE1235281B (de) | 1965-07-13 | 1965-07-13 | Verfahren zur Herstellung von Hartwachsen |
| GB3150866A GB1150933A (en) | 1965-07-13 | 1966-07-13 | Process for preparing hard waxes |
| FR69369A FR1486708A (fr) | 1965-07-13 | 1966-07-13 | Procédé de préparation de cires |
| BE684080D BE684080A (enrdf_load_stackoverflow) | 1965-07-13 | 1966-07-13 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF46581A DE1235281B (de) | 1965-07-13 | 1965-07-13 | Verfahren zur Herstellung von Hartwachsen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1235281B true DE1235281B (de) | 1967-03-02 |
Family
ID=7101117
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEF46581A Pending DE1235281B (de) | 1965-07-13 | 1965-07-13 | Verfahren zur Herstellung von Hartwachsen |
Country Status (3)
| Country | Link |
|---|---|
| BE (1) | BE684080A (enrdf_load_stackoverflow) |
| DE (1) | DE1235281B (enrdf_load_stackoverflow) |
| GB (1) | GB1150933A (enrdf_load_stackoverflow) |
-
1965
- 1965-07-13 DE DEF46581A patent/DE1235281B/de active Pending
-
1966
- 1966-07-13 BE BE684080D patent/BE684080A/xx unknown
- 1966-07-13 GB GB3150866A patent/GB1150933A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| BE684080A (enrdf_load_stackoverflow) | 1967-01-13 |
| GB1150933A (en) | 1969-05-07 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0003112A1 (de) | Verfahren zur Herstellung von Polybutylenglykolcarbonsäurediester durch Polymerisation von chemisch vorbehandeltem Tetrahydrofuran | |
| DE1150206B (de) | Verfahren zur Herstellung von Polymerisaten aus Olefinoxyden | |
| DE1086226B (de) | Verfahren zur Herstellung von Cyclododecatrien-(1, 5, 9) | |
| DE1246711B (de) | Verfahren zur Herstellung oeliger Polymerisationsprodukte aus AEthylen | |
| DE2633745A1 (de) | Verfahren zur herstellung von polyolefinoelen | |
| DE1495868B2 (de) | Verfahren zur Herstellung von Acyloxyalkylgruppen enthaltenden Organopolysiloxanen | |
| DE3737920A1 (de) | Verfahren zur herstellung von perfluorierten carbonsaeurefluoriden | |
| DE1520900C3 (de) | Verfahren zum Polymerisieren von Olefinen | |
| DE1235281B (de) | Verfahren zur Herstellung von Hartwachsen | |
| DE2801578A1 (de) | Verfahren zur polymerisation von tetrahydrofuran | |
| DE1645115B1 (de) | Verfahren zur Herstellung von Hexafluorpropylenepoxyd-Polymerisaten | |
| DE2437093C2 (de) | Verfahren zur Verhinderung der Vernetzung von Vinylchlorid-Vinyltrialkoxysilan-Copolymerisaten | |
| DE1233378C2 (de) | Verfahren zum reinigen von propylenoxyd | |
| DE1250421B (de) | Verfahren zur Herstellung von wachsartigen löslichen Polyestern | |
| DE1038283B (de) | Verfahren zur Herstellung neuartiger Epoxyverbindungen | |
| DE2047140A1 (de) | Verfahren zur Herstellung von Polypropylen und/oder Polybutylen Ölen | |
| DE1262275B (de) | Verfahren zur Herstellung von Hartwachsen | |
| DE3837506A1 (de) | Verfahren zur herstellung von oligomeren des hexafluorpropenoxids | |
| DE1257435B (de) | Verfahren zur Herstellung von Polysiloxanen mit endstaendig ungesaettigten Gruppen | |
| DE1045662B (de) | Verfahren zur Herstellung von Mischpolymerisaten aus Tetrahydrofuran und Olefinoxyden | |
| DE1495733C (de) | Verfahren zur Herstellung von Oxymethylen Blockcopolymerisaten | |
| DE1257129B (de) | Verfahren zur Herstellung von harten, loeslichen Esterwachsen | |
| DE1261844B (de) | Verfahren zur Herstellung von AEtherwachsen | |
| DE671750C (de) | Verfahren zur Herstellung von Kunstharzen | |
| DE1908340C3 (de) | 2-Norbornen-Verbindungen, Verfahren zu ihrer Herstellung und ihre Verwendung als Comonomere zur Herstellung von Copolymerisaten |