DE1420206A1 - Verfahren zur Herstellung von Polymerisationsprodukten aus olefinisch ungesaettigtenVerbindungen - Google Patents
Verfahren zur Herstellung von Polymerisationsprodukten aus olefinisch ungesaettigtenVerbindungenInfo
- Publication number
- DE1420206A1 DE1420206A1 DE19551420206 DE1420206A DE1420206A1 DE 1420206 A1 DE1420206 A1 DE 1420206A1 DE 19551420206 DE19551420206 DE 19551420206 DE 1420206 A DE1420206 A DE 1420206A DE 1420206 A1 DE1420206 A1 DE 1420206A1
- Authority
- DE
- Germany
- Prior art keywords
- parts
- olefinically unsaturated
- unsaturated compounds
- preparation
- polymerization products
- 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
- 150000001875 compounds Chemical class 0.000 title claims description 9
- 238000006116 polymerization reaction Methods 0.000 title claims description 6
- 238000000034 method Methods 0.000 title claims description 4
- 238000002360 preparation method Methods 0.000 title claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 239000003054 catalyst Substances 0.000 claims description 6
- -1 aryl compound Chemical class 0.000 claims description 5
- 150000004820 halides Chemical class 0.000 claims description 5
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- 230000000737 periodic effect Effects 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- MRMOZBOQVYRSEM-UHFFFAOYSA-N tetraethyllead Chemical compound CC[Pb](CC)(CC)CC MRMOZBOQVYRSEM-UHFFFAOYSA-N 0.000 description 8
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 6
- 239000005977 Ethylene Substances 0.000 description 6
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 4
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 4
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 4
- 238000001816 cooling Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 2
- 150000002366 halogen compounds Chemical class 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- RWWNQEOPUOCKGR-UHFFFAOYSA-N tetraethyltin Chemical compound CC[Sn](CC)(CC)CC RWWNQEOPUOCKGR-UHFFFAOYSA-N 0.000 description 2
- 238000010792 warming Methods 0.000 description 2
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 1
- 238000006418 Brown reaction Methods 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 241001582367 Polia Species 0.000 description 1
- 208000000474 Poliomyelitis Diseases 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229910021552 Vanadium(IV) chloride Inorganic materials 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- 229910007926 ZrCl Inorganic materials 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical group FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 description 1
- 229940117389 dichlorobenzene Drugs 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- BXVLQFGQYHYURU-UHFFFAOYSA-N diethyltin Chemical compound CC[Sn]CC BXVLQFGQYHYURU-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- 239000003701 inert diluent Substances 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000005673 monoalkenes Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- 125000003107 substituted aryl group Chemical group 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- UAPQJVJCJITJET-UHFFFAOYSA-N triphenyltin Chemical compound C1=CC=CC=C1[Sn](C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1[Sn](C=1C=CC=CC=1)C1=CC=CC=C1 UAPQJVJCJITJET-UHFFFAOYSA-N 0.000 description 1
- JTJFQBNJBPPZRI-UHFFFAOYSA-J vanadium tetrachloride Chemical compound Cl[V](Cl)(Cl)Cl JTJFQBNJBPPZRI-UHFFFAOYSA-J 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 238000004804 winding Methods 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
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEB0037136 | 1955-09-09 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1420206A1 true DE1420206A1 (de) | 1968-10-31 |
Family
ID=6965120
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19551420206 Pending DE1420206A1 (de) | 1955-09-09 | 1955-09-09 | Verfahren zur Herstellung von Polymerisationsprodukten aus olefinisch ungesaettigtenVerbindungen |
Country Status (5)
| Country | Link |
|---|---|
| BE (1) | BE550840A (enrdf_load_stackoverflow) |
| DE (1) | DE1420206A1 (enrdf_load_stackoverflow) |
| FR (1) | FR1160375A (enrdf_load_stackoverflow) |
| GB (1) | GB798447A (enrdf_load_stackoverflow) |
| IT (1) | IT558973A (enrdf_load_stackoverflow) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE586479A (enrdf_load_stackoverflow) * | 1959-01-12 | |||
| BE602439A (enrdf_load_stackoverflow) * | 1960-04-13 |
-
0
- IT IT558973D patent/IT558973A/it unknown
- BE BE550840D patent/BE550840A/xx unknown
-
1955
- 1955-09-09 DE DE19551420206 patent/DE1420206A1/de active Pending
-
1956
- 1956-09-03 GB GB2682156A patent/GB798447A/en not_active Expired
- 1956-09-07 FR FR1160375D patent/FR1160375A/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| GB798447A (en) | 1958-07-23 |
| IT558973A (enrdf_load_stackoverflow) | |
| FR1160375A (fr) | 1958-07-15 |
| BE550840A (enrdf_load_stackoverflow) |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2350196C2 (de) | Verfahren zur Polymerisation von Äthylen | |
| DE1052689B (de) | Verfahren zur Herstellung von hochmolekularen Polymerisaten der Acetylenkohlenwasserstoffe | |
| DE1112297B (de) | Verfahren zur Herstellung fester oder halbfester AEthylenpolymerisate | |
| DE3148229A1 (de) | Verfahren zur herstellung von polyolefinwachsen | |
| DE1420662A1 (de) | Verfahren zum Polymerisieren endstaendig ungesaettigter Kohlenwasserstoffe | |
| DE1595708A1 (de) | Verfahren zur Herstellung von Mischpolymerisaten des Vinylchlorids | |
| DE1420206A1 (de) | Verfahren zur Herstellung von Polymerisationsprodukten aus olefinisch ungesaettigtenVerbindungen | |
| DE1104182B (de) | Polymerisationskatalysator fuer die Block- und Loesungspolymerisation | |
| DE1016018B (de) | Verfahren zur Herstellung von Polymerisaten aus Olefinen | |
| DE1795467A1 (de) | Verfahren zur Herstellung von Polyamiden durch Polymerisieren von epsilon-Caprolactam | |
| DE1420482A1 (de) | Verfahren zur Polymerisation von Lactamen | |
| DE1178431B (de) | Verfahren zur Herstellung von polymeren Zinnalkylenchloriden | |
| DE1907242A1 (de) | Polymerisationskatalysator und kationische Polymerisation | |
| DE1645250C3 (de) | Verfahren zur Herstellung von isotaktischen Polyolefinen | |
| DE2047140A1 (de) | Verfahren zur Herstellung von Polypropylen und/oder Polybutylen Ölen | |
| DE1176867B (de) | Verfahren zur Herstellung von Polybuten | |
| AT205961B (de) | Verfahren zum Dimerisieren von niederen α-Olefinen | |
| DE1645150A1 (de) | Cyclobutancarbonitrilpolymerisate und Verfahren zu ihrer Herstellung | |
| DE1668300A1 (de) | Neue organometallische Komplexe und ihre Anwendung bei der Herstellung von Katalysatoren fuer die Oligomerisation,Polymerisation und Copolymerisation von ungesaettigten Kohlenwasserstoffen | |
| DE736504C (de) | Verfahren zur Herstellung von ª‡-Acetoxyacrylnitril | |
| DE2721377C2 (enrdf_load_stackoverflow) | ||
| DE1720419A1 (de) | Katalysator zur stereoregulaeren Polymerisation von C3-bis C6-Mono-alpha-olefinen | |
| AT229571B (de) | Verfahren zur Herstellung hochmolekularer, linearer, amorpher Copolymere von Äthylen mit höheren α - Olefinen | |
| AT271878B (de) | Verfahren zur Herstellung von Vinylchlorid-Polymerisaten | |
| DE2524921C3 (enrdf_load_stackoverflow) |