Process for isolating pure 2-ethylhexyl acrylate or pure 2-propylheptyl acrylate from the corresponding crude alkyl acrylate by distillation

Patent metadata

Field	Value
Publication number	US-10894223-B2
Application number	US-201716472054-A
Country	US
Kind code	B2
Filing date	Dec 11, 2017
Priority date	Dec 21, 2016
Publication date	Jan 19, 2021
Grant date	Jan 19, 2021

Abstract

Process for isolating pure 2-ethylhexyl acrylate or pure 2-propylheptyl acrylate from the corresponding crude alkyl acrylate by distillation, wherein the process is carried out in a dividing wall column (1) which has separation-active internals and vaporizer (7) and in which a dividing wall (8) is arranged in the longitudinal direction of the column to form an upper joint column region (9), a lower joint column region (14), an inflow section (10, 12) having a side feed point (2) and an offtake section (11, 13) having a side offtake point (3), the column has a number of theoretical plates in the range from 10 to 60, where the number of theoretical plates of the dividing wall column (1) relates to the sum of the theoretical plates in the joint upper column region (9), the joint lower column region (14) and the inflow section (10, 12), the side feed point (2) for the corresponding crude alkyl acrylate is arranged at a theoretical plate in the region commencing at least two theoretical plates above the bottommost theoretical plate and ending at least two theoretical plates below the uppermost theoretical plate, the side offtake point (3) for the pure 2-ethylhexyl acrylate or pure 2-propylheptyl acrylate is arranged at a theoretical plate in the region commencing at least two theoretical plates above the bottommost theoretical plate and ending at least two theoretical plates below the uppermost theoretical plate and the dividing wall (8) is arranged in the column in the region commencing at least one theoretical plate above the bottommost theoretical plate and ending at least one theoretical plate below the uppermost theoretical plate, where the ratio of amount of liquid at the upper end of the dividing wall (8) going to the enrichment section (10) and the stripping section (11) of the column is set in the range from 1:0.2 to 1:5.

First claim

The invention claimed is:

1. A process for purifying 2-propylheptyl acrylate from a corresponding crude alkyl acrylate, the process comprising:
distilling the corresponding crude alkyl acrylate in a dividing wall column,
wherein the dividing wall column has separation-active internals and a vaporizer and in which a dividing wall is arranged in a longitudinal direction of the dividing wall column to form an upper joint column region, a lower joint column region, an inflow section having a side feed point and a side offtake section having a side offtake point,
wherein the dividing wall column has a number of theoretical plates in the range from 10 to 60, where the number of theoretical plates of the dividing wall column relates to the sum of the theoretical plates in the joint upper column region, the joint lower column region and the inflow section,
wherein in the dividing wall column the side feed point for the corresponding crude alkyl acrylate is arranged at a theoretical plate in a region commencing at least two theoretical plates above a bottommost theoretical plate and ending at least two theoretical plates below an uppermost theoretical plate, the side offtake point for a distilled 2-propylheptyl acrylate is arranged at a theoretical plate in the region commencing at least two theoretical plates above the bottommost theoretical plate and ending at least two theoretical plates below the uppermost theoretical plate, and the dividing wall is arranged in the dividing wall column in a region commencing at least one theoretical plate above the bottommost theoretical plate and ending at least one theoretical plate below the uppermost theoretical plate,
where a ratio of an amount of liquid at the upper end of the dividing wall going to an enrichment section and an amount of liquid at a stripping section of the dividing wall column is in the range from 1:0.2 to 1:5 and a ratio of amounts of a vapor stream at the lower end of the dividing wall going to the stripping section and a vapor stream at the enrichment section of the dividing wall column is in the range from 1:0.5 to 1:2.0, wherein the upper end is above the side feed point and the lower end is below the side offtake point; and
wherein the distilling includes isolating 2-propylheptyl acrylate having a purity of ≥98.5% by weight from the corresponding crude alkyl acrylate.

2. The process according to claim 1 , wherein the side feed point for the corresponding crude alkyl acrylate is arranged at a theoretical plate in a region commencing at least four theoretical plates above the bottommost theoretical plate and ending at least four theoretical plates below the uppermost theoretical plate, the side offtake point for the distilled 2-propylheptyl acrylate is arranged at a theoretical plate in the region commencing at least four theoretical plates above the bottommost theoretical plate and ending at least four theoretical plates below the uppermost theoretical plate and the dividing wall in the dividing wall column is arranged in the region commencing at least two theoretical plates above the bottommost theoretical plate and ending at least two theoretical plates below the uppermost theoretical plate.

3. The process according to claim 1 , wherein the dividing wall column has a number of theoretical plates in the range from 15 to 30, the side feed point for the corresponding crude alkyl acrylate is arranged at a theoretical plate in a region commencing at least eight theoretical plates above the bottommost theoretical plate and ending at least six theoretical plates below the uppermost theoretical plate, the side offtake point for the distilled 2-propylheptyl acrylate is arranged at a theoretical plate in a region commencing at least five theoretical plates above the lowermost theoretical plate and ending at least eight theoretical plates below the uppermost theoretical plate and the dividing wall in the column is arranged in a region commencing at least three theoretical plates above the bottommost theoretical plate and ending at least three theoretical plates below the uppermost theoretical plate.

4. The process according to claim 1 , wherein an opposite side offtake point is located at least one theoretical plate below the side feed point, where in the case of different numbers of theoretical plates in the side offtake section and the inflow section, the side having the greatest total number of theoretical plates in the region of the dividing wall is a basis for counting the number of theoretical plates for determining the relative height position of the feed point and the offtake point.

5. The process according to claim 1 , wherein the dividing wall column comprises one or more separation-active internals selected from the group consisting of a random packing element, an ordered packing and a tray.

6. The process according to claim 5 , wherein the dividing wall column comprises dual-flow trays.

7. The process according to claim 6 , wherein dual-flow trays on the inflow side and dual-flow trays on the offtake side have different opening ratios for gas distribution.

8. The process according to claim 1 , wherein during the distilling a residence time of material in the vaporizer and piping in proximity of and fluidly connected to the vaporizer is from 1 to 60 minutes.

9. The process according to claim 1 , wherein the ratio of the amount of the liquid at the upper end of the dividing wall going to the enrichment section and the amount of the liquid going to the stripping section of the dividing wall column is in the range from 1:0.5 to 1:2.

10. The process according to claim 1 , wherein the ratio of the amount of the vapor stream at the lower end of the dividing wall going to the stripping section and the amount of the vapor stream at the enrichment section of the dividing wall column is in the range from 1:0.9 to 1:1.5.

11. The process according to claim 1 , wherein during the distilling a pressure at the top of the dividing wall column is in the range from 10 mbar to 5 bar.

12. The process according to claim 1 , wherein the dividing wall column further comprises a temperature controller in the upper joint column region, wherein the temperature controller receives a temperature signal below the uppermost theoretical plate, and the process further comprises:
changing at least one of a distillate flow, a reflux ratio and an amount of reflux.

13. The process according to claim 1 , wherein the dividing wall column further comprises a temperature controller in the lower joint column region, wherein the temperature controller receives a temperature signal above the bottommost theoretical plate, and the process further comprises:
changing an amount of material taken off at the bottom of the dividing wall column.

14. The process according to claim 1 , wherein the dividing wall column further comprises a level controller at the bottom of the dividing wall column, and the process further comprises:
changing an amount of material taken off at the side of the dividing wall column.

15. The process according to claim 1 , wherein a ratio of a cross-sectional area of a region of the offtake section to a cross-sectional area of a region of the inflow section is from 4:1 to 1:4.

16. The process according to claim 1 , wherein a ratio of a cross-sectional area of a region of the offtake section to a cross-sectional area of a region of the inflow section is from 1.5:1 to 1:1.5.

17. The process according to claim 1 , wherein the corresponding crude alkyl acrylate has the following composition:
from 40 to 99% by weight of 2-propylheptyl acrylate,
from 0.

Assignees

• Basf Se

Inventors

• Lang Ortmund
• Metzen Bernd
• Hechler Claus

Classifications

• C07C69/54

  Acrylic acid esters; Methacrylic acid esters · CPC title

• C07C67/54 Primary

  by distillation · CPC title

• B01D3/00

  Distillation or related exchange processes in which liquids are contacted with gaseous media, e.g. stripping ({evaporation in general, e.g. of liquids for gas phase reactions B01B1/005;} gas chromatography B01D15/08; destructive distillation C10B; preparation of alcoholic beverages by distillation C12H6/02) · CPC title

• B01D3/225

  Dual-flow sieve trays · CPC title

• B01D3/4283

  Bottom stream · CPC title