Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methyl Benzoate | HCID 7150 | — |
| Edukt | 1-Hexanol | HCID 8103 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 1-Hexanol | HCID 8103 | — |
| Produkt | Hexyl Acetate | HCID 8908 | — |
Reaktionsschritte
The data in Table 2 was obtained in the following manner. The charge was brought to boiling and after a half hour of operation in the 4.5 theoretical plate column to establish equilibrium throughout, methylbenzoate at 95° C. and 10-16 ml/min. was pumped in. The rectification was continued for 11/4 hours with sampling of the overhead and bottoms after 75 minutes. The analysis is shown in Table 2 and was 97.3% n-hexyl alcohol in the overhead and 81% n-hexyl alcohol in the bottoms, both on a water-free basis, which gives a relative volatility of 1.605 of n-hexyl alcohol to n-hexyl acetate. This indicates that the ternary azeotrope has been negated and the separation accomplished. The n-hexyl alcohol comes off in the form of its binary azeotrope with water which on condensation, immediately forms two layers. The solubility of n-hexyl alcohol in liquid water is only 0.6%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04673466 |
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| Quelldatensatz | uspto-grants-1987_06 |
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| ORD ID | ord-d3439c9293a94133bf774bfdd982884a |
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| Quellennotiz | uspto-grants-1987_06 |
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