Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethylene | HCID 6325 | — |
| Edukt | 1-Octene | HCID 8125 | — |
| Edukt | N,N-dimethylanilinium tetrakis(pentafluorophenyl)borate | HCID 10996402 | — |
| Edukt | Triisobutylaluminum | HCID 16682931 | — |
| Edukt | HCID 178418750 | HCID 178418750 | — |
| Lösungsmittel | Hexane | HCID 8058 | — |
| Produkt | Ethene;oct-1-ene | HCID 168495 | — |
Reaktionsschritte
Under the pressure of 89 bar, 1-octene and ethylene as monomers and a hexane solvent (3.20 kg/h) were fed into a 1.5 L continuous stirred tank reactor preheated up to 100 to 150° C. Into the reactor were fed a catalyst A, a catalyst B, and a dimethylanilinium tetrakis(pentafluorophenyl) borate cocatalyst from a catalyst storage tank and then added a scavenger (TIBAL) and diethyl zinc to activate a copolymerization reaction. The scavenger was first mixed with reactants in order to eliminate impurities potentially contained in the reactants and then fed into the reactor. In the Examples, the polymerization reaction was carried out at a relatively high temperature of 140 to 150° C., and the polymer solution resulting from the copolymerization reaction was transferred into a solvent separator to remove most of the solvent. The resultant solution was passed through a cooling water and a cutter to yield a granulated polymer product. The polymerization conditions for ethylene and 1-octene according to the Comparative Examples 1 and 2 and Examples 1 to 10 are presented in the following Table 1.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09035006B2 |
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| Quelldatensatz | uspto-grants-2015_05 |
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| ORD ID | ord-154d3b16e3444c2cbf80002b8b95097b |
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| Quellennotiz | uspto-grants-2015_05 |
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