関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1-Octene | HCID 8125 | — |
| 反応物 | Butyl ether | HCID 8909 | — |
| 反応物 | 1-Decene | HCID 13381 | — |
| 反応物 | Aluminum | HCID 5359268 | — |
| 反応物 | Diisobutyl aluminium chloride | HCID 16686353 | — |
| 溶媒 | Heptane | HCID 8900 | — |
| 生成物 | 1-Decene, adduct with 1-octene (1:1) | HCID 162200 | — |
反応手順
A catalyst was prepared by combining, in a primarily nitrogen environment under ambient temperature and pressure, 2.92 grams of TiCl3.AA with 23.07 grams of purified petroleum distillate, together with 2.05 grams of dibutyl ether promoter according to the teachings of Mack U.S. Pat. No. 4,416,714. The solution was held for 30 minutes while stirring. The catalyst was then activated using 20.71 grams of an aluminum cocatalyst, a 25% solution of diisobutyl aluminum chloride (DIBAC) in heptane solvent (“25% DIBAC solution”). Again, the mixture was held for 30 minutes while stirring. An octene-decene copolymer was prepared in a primarily nitrogen environment under standard temperature and pressure by mixing 381.2 grams of octene with 119.0 grams of decene in a beaker. After stirring, 4.0 milliliters of a 25% DIBAC solution was added to the beaker. The mixture was held for 30 minutes without stirring. A 3.0 milliliter portion of the catalyst mixture prepared was added to the beaker while stirring continuously. The entire mixture was allowed to react. The subsequent copolymer was subsequently tested and found to have a 95.53% conversion to polymer with an inherent viscosity of 27.8 deciliters/gram.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06596832B2 |
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| 出典データセット | uspto-grants-2003_07 |
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| ORD ID | ord-a33c7330270c4f699591d3dd05b09957 |
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| 出典メモ | uspto-grants-2003_07 |
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