Simplified process for isolating pure 1,3-butadiene

Patent metadata

Field	Value
Publication number	US-10968152-B2
Application number	US-201816493185-A
Country	US
Kind code	B2
Filing date	Mar 12, 2018
Priority date	Mar 13, 2017
Publication date	Apr 6, 2021
Grant date	Apr 6, 2021

Abstract

A process for isolating pure 1,3-butadiene from a crude C 4 fraction, which produces pure 1,3-butadiene having a prescribed maximum content of at least one low boiler and a prescribed maximum content of 1,2-butadiene, in each case based on 1,3-butadiene, wherein (a) a low boiler fraction and a high boiler fraction are separated off by distillation from the crude C 4 fraction, giving a purified C 4 fraction whose content of the at least one low boiler, based on 1,3-butadiene, is equal to or lower than the prescribed maximum content of the at least one low boiler and whose content of 1,2-butadiene, based on 1,3-butadiene, is equal to or lower than the prescribed maximum content of 1,2-butadiene; (b) the purified C 4 fraction is subjected to at least one extractive distillation using a selective solvent, giving at least a fraction comprising butanes and butenes and a pure 1,3-butadiene fraction, is described. The process makes a pure distillation column dispensable.

First claim

The invention claimed is:

1. A process for isolating pure 1,3-butadiene from a crude C 4 fraction, the process comprising:
introducing the crude C 4 fraction into a predistillation column comprising a dividing wall running in a longitudinal direction of the predistillation column, and taking off a C 3 low boiler fraction, comprising C 3 hydrocarbons, as an overhead stream from the predistillation column, taking off a high boiler fraction as a bottom stream from the predistillation column, and taking off a purified C 4 fraction as a side stream from the predistillation column;
extractively distilling the purified C 4 fraction using a selective solvent to obtain a fraction comprising butanes and butenes and a pure 1,3-butadiene fraction comprising at least 99.5 wt. % 1,3-butadiene,
wherein the purified C 4 fraction comprises a lower boiler in an amount equal to or lower than a prescribed maximum lower boiler content and 1,2-butadiene in an amount equal to or lower than a prescribed maximum 1,2-butadiene content, and
wherein the prescribed maximum 1,2-butadiene content is 25 ppm, based on 1,3-butadiene.

2. The process of claim 1 , wherein the low boiler is propyne.

3. The process of claim 2 , wherein the prescribed maximum content of propyne is 20 ppm, based on 1,3-butadiene.

4. The process of claim 3 , wherein the prescribed maximum 1,2-butadiene content is 15 ppm, based on 1,3-butadiene.

5. The process of claim 1 , wherein the extractively distilling comprises:
obtaining a loaded solvent fraction comprising 1,3-butadiene and the selective solvent, and desorbing crude 1,3-butadiene from the loaded solvent fraction, and
scrubbing the crude 1,3-butadiene in a rectification zone comprising at least two theoretical plates with liquid 1,3-butadiene obtained by condensation of a vapor obtained at a top of the rectification zone, giving the pure 1,3-butadiene fraction.

6. The process of claim 5 , wherein an acetylene fraction is also desorbed from the loaded solvent fraction, giving an outgassed selective solvent.

7. The process of claim 6 , wherein the crude 1,3-butadiene is extracted with the outclassed selective solvent before the scrubbing with the liquid 1,3-butadiene.

8. The process of claim 7 , wherein the extractively distilling comprises:
contacting the purified C 4 fraction with the selective solvent in at least one extraction column, giving an overhead fraction comprising butanes and butenes and a bottom fraction comprising 1,3-butadiene and the selective solvent;
desorbing the crude 1,3-butadiene from the bottom fraction, giving a preoutgassed selective solvent;
desorbing acetylenes from the preoutgassed selective solvent, giving the outgassed selective solvent;
extracting the crude 1,3-butadiene with the outgassed selective solvent in an after-scrubbing zone; and
scrubbing the extracted crude 1,3-butadiene with the liquid 1,3-butadiene in the rectification zone, giving the pure 1,3-butadiene fraction.

9. The process of claim 8 , wherein the rectification zone is arranged above the after-scrubbing zone in a column or a column section.

10. The process of claim 8 , wherein the purified C 4 fraction is brought into contact with the selective solvent in an extraction column and in an upper section of an extraction and preoutgassing column and the crude 1,3-butadiene is desorbed from the bottom fraction in a lower section of the extraction and preoutgassing column and an outgassing column.

11. The process of claim 10 , wherein the after-scrubbing zone and the rectification zone are formed in an upper section of the extraction and preoutgassing column which is separated by a dividing wall running in a longitudinal direction of the column.

12. The process of claim 10 , wherein an outgassing column is operated at the same pressure level as the extraction and preoutgassing column and an overhead product from the outgassing column is recirculated without increasing pressure into the extraction and preoutgassing column.

13. The process of claim 8 , wherein a part of the vapor which has not been condensed at the top of the rectification zone is conveyed together with the vapor from the predistillation column through an overhead condenser of the predistillation column.

14. The process of claim 1 , further comprising:
separating off dissolved water from the pure 1,3-butadiene fraction.

15. The process of claim 14 , wherein the separating off of the water comprises cooling and phase separating and/or stripping in a stripping column.

16. The process of claim 1 , wherein the selective solvent comprises at least 80% by weight of N-methylpyrrolidone.

17. The process of claim 1 , wherein the love boiler comprises propyne.

18. The process of claim 1 , wherein the selective solvent comprises acetonitrile, propionitrile, methoxypropionitrile, acetone, furfuryl alcohol, dimethylformamide, diethylformamide, dimethylacetamide, diethylacetamide, N-formylmorpholine, and/or N-methylpyrrolidone.

19. The process of claim 1 , wherein the selective solvent comprises dimethylformamide, acetonitrile, or furfuryl alcohol.

Assignees

• Basf Se

Inventors

• Heida Bernd
• Keller Tobias

Classifications

• C07C7/08 Primary

  by extractive distillation · CPC title

• C07C7/04 Primary

  by distillation · CPC title

• B01D3/40

  Extractive distillation · CPC title

• B01D3/143

  by two or more of a fractionation, separation or rectification step · CPC title

• C07C11/167 Primary

  1, 3-Butadiene · CPC title