Method for preparing hexane from aromatic hydrocarbon raffinate oil
A technology for raffinate oil and aromatics, applied in the production of n-hexane, isohexane and cyclohexane, which can solve the problems of low yield of cyclohexane, low added value of products, and low yield of n-hexane
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0046] according to figure 1 Shown is a method for preparing hexane from aromatic hydrocarbon raffinate.
[0047] Containing 10wt% C5 and below components, 15wt% isohexane, 8wt% n-hexane, 20wt% methylcyclopentane, 5wt% cyclohexane and 0.1% benzene aromatics raffinate F enters the first rectification column, from The top of the first rectification column obtains stream I containing C5 and below components, the side line position obtains stream II containing isohexane, n-hexane, methylcyclopentane and benzene, and the position below the feed obtains C7 and above containing cyclohexane Component stream III, stream II obtains stream IV through a hydrogenation reactor, and stream IV obtains stream V containing isohexane, normal hexane, and hexanaphthene through an isomerization reactor, and stream V passes through such as figure 2 The shown isohexane tower, n-hexane tower, methylcyclopentane tower, and cyclohexane tower are sequentially separated to obtain isohexane, n-hexane, m...
Embodiment 2
[0053] Implementation is similar to Example 1. Containing 10wt% C5 and below components, 15wt% isohexane, 8wt% n-hexane, 20wt% methylcyclopentane, 5wt% cyclohexane and 0.1% benzene aromatics raffinate F enters the first rectification column, from The top of the first rectification column obtains stream I containing C5 and below components, the side line position obtains stream II containing isohexane, n-hexane, methylcyclopentane and benzene, and the position below the feed obtains C7 and above containing cyclohexane Component stream III, stream II obtains stream IV through a hydrogenation reactor, and stream IV obtains stream V containing isohexane, normal hexane, and hexanaphthene through an isomerization reactor, and stream V passes through such as figure 2 The shown isohexane tower, n-hexane tower, methylcyclopentane tower, and cyclohexane tower are sequentially separated to obtain isohexane, n-hexane, methylcyclopentane, and cyclohexane, wherein methylcyclopentane is rec...
Embodiment 3
[0061] Implementation is similar to Example 1. Containing 1wt% C5 and below components, 15wt% isohexane, 8wt% n-hexane, 20wt% methylcyclopentane, 5wt% cyclohexane and 0.1% benzene aromatics raffinate F enters the first rectification column, from The top of the first rectification column obtains stream I containing C5 and below components, the side line position obtains stream II containing isohexane, n-hexane, methylcyclopentane and benzene, and the position below the feed obtains C7 and above containing cyclohexane Component stream III, stream II obtains stream IV through a hydrogenation reactor, and stream IV obtains stream V containing isohexane, normal hexane, and hexanaphthene through an isomerization reactor, and stream V passes through such as figure 2 The shown isohexane tower, n-hexane tower, methylcyclopentane tower, and cyclohexane tower are sequentially separated to obtain isohexane, n-hexane, methylcyclopentane, and cyclohexane, wherein methylcyclopentane is recy...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 


