関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-Pentenoic acid | HCID 12299 | — |
| 溶媒 | 1-Butanol | HCID 263 | — |
| 生成物 | Carbon Dioxide | HCID 280 | 67% |
| 生成物 | Propanal | HCID 527 | 2% |
| 生成物 | 1-Butene | HCID 7844 | — |
反応手順
An appropriate (and preferred) compromise between obtaining a high rate of GVL conversion and maintaining stable catalyst operation is achieved using an aqueous feed solution containing about 60 wt % GVL at 648 K and at a pressure of about 36 bar (see Table 1, entry 5). Under these conditions, catalytic activity remains constant for over 100 h of time on stream (see FIG. 4 and the accompanying text in the Examples). Under these reaction conditions, the following yields were obtained: 85% conversion of the GVL feed to form butene and stoichiometric CO2 (67% yield), pentenoic acid isomers (15% yield), small oxygenates such as butanol and propionaldehyde (2% yield), and aromatization/oligomerization products including octene and ethylbenzene (1% yield). The butene yield is limited by the unconverted pentenoic acid intermediate, and yields in excess of 90% are achieved using a 60 wt % feed at lower space velocities (Table 1, entry 7) with 100% of GVL conversion. Under these reaction conditions, pentenoic acid was not observed, and 93% yield to butene was achieved. The fraction of butene converted to C8+ alkenes and aromatics increased and accounted for the remainder of products observed (7% yield). The percentage of butene present as 1-butene (33%) compared to cis/trans 2-butene (67%) was higher than thermodynamic equilibrium, suggesting that 1-butene is the primary product.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08410326B2 |
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| 出典データセット | uspto-grants-2013_04 |
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| ORD ID | ord-34cd99527ffa4cefbc14897c5bab00fb |
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| 出典メモ | uspto-grants-2013_04 |
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