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C[O:2][C:3](=O)[C:4]1C=[CH:8][CH:7]=[CH:6][CH:5]=1.[CH2:11]([OH:17])[CH2:12][CH2:13][CH2:14][CH2:15][CH3:16]>O>[CH2:3]([OH:2])[CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[C:3]([O:17][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16])(=[O:2])[CH3:4]참가 물질
실험 절차
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%.
후처리
- customThe data in Table 2 was obtained in the following manner
- waitto boiling and after a half hour of operation in the 4.5 theoretical plate column
- customat 95° C.
- custom4 hours
- aliquotwith sampling of the overhead and bottoms after 75 minutes
출처 및 근거
- ORD 기록
- ord-d3439c9293a94133bf774bfdd982884a
- 출처 데이터셋
- uspto-grants-1987_06
- 특허 번호
- US04673466
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