IP Library Granted Patent US 8,049,028
Granted Patent B2
US 8,049,028 · App. 11/991,073 · Granted Nov 1, 2011

Industrial process for separating out dialkyl carbonate

Assignee: Asahi Kasei Chemicals Corporation
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Quick Facts
Patent No.
US 8,049,028
App. No.
11/991,073
Granted
Nov 1, 2011
Kind
B2
Abstract

It is an object of the present invention to provide a specific apparatus and process for using a single distillation column on a low boiling point reaction mixture containing a large amount of a dialkyl carbonate and an aliphatic monohydric alcohol produced through a reactive distillation process of taking a cyclic carbonate and the aliphatic monohydric alcohol as starting materials, continuously feeding the starting materials into a continuous multi-stage distillation column in which a homogeneous catalyst is present, and carrying out reaction and distillation simultaneously in the column, so as to separate the low boiling point reaction mixture by distillation into a column top component B T having the aliphatic monohydric alcohol as a main component thereof and a column bottom component B B having the dialkyl carbonate as a main component thereof stably for a prolonged period of time industrially.

Claims (33)

1. In an industrial process for separating out a dialkyl carbonate, comprising the steps of:

continuously feeding starting materials into a continuous multi-stage distillation column A in which a homogeneous catalyst is present by taking a cyclic carbonate and an aliphatic monohydric alcohol as the starting materials;

carrying out reactive distillation in said column A;

continuously withdrawing a high boiling point reaction mixture A B containing a produced diol from a lower portion of said column A in a liquid form;

continuously withdrawing a low boiling point reaction mixture A T containing a produced dialkyl carbonate and the aliphatic monohydric alcohol from an upper portion of said column A in a gaseous form;

continuously feeding said low boiling point reaction mixture A T into a continuous multi-stage distillation column B; and

carrying out separation by distillation into a column top component B T having the aliphatic monohydric alcohol as a main component thereof and a column bottom component B B having the dialkyl carbonate as a main component thereof, wherein the improvement which comprises:

said continuous multi-stage distillation column B comprises a distillation column comprising a stripping section having a length L 1 (cm), an inside diameter D 1 (cm) and an internal with a number of stages n 1 thereinside, and an enrichment section having a length L 2 (cm), an inside diameter D 2 (cm) and an internal with a number of stages n 2 thereinside, wherein L 1 , D 1 , n 1 , L 2 , D 2 , and n 2 satisfy the following formulae (1) to (8);

500≦L 1 ≦3000  (1)

100≦D 1 ≦1000  (2)

2 ≦L 1 /D 1 ≦30  (3)

10≦n 1 ≦40  (4)

700≦L 2 ≦5000  (5)

50≦D 2 ≦800  (6)

10 ≦L 2 /D 2 ≦50  (7), and

35≦n 2 ≦100  (8).

2. The process according to claim 1 , wherein L 1 , D 1 , L 1 /D 1 , n 1 , L 2 , D 2 , L 2 /D 2 , and n 2 for said continuous multi-stage distillation column B satisfy 800≦L 1 ≦2500, 120≦D 1 ≦800, 5≦L 1 /D 1 ≦20, 13≦n 1 ≦25, 1500≦L 2 ≦3500, 70≦D 2 ≦600, 15≦L 2 /D 2 ≦30, 40≦n 2 ≦70, L 1 ≦L 2 , and D 2 ≦D 1 .

3. The process according to claim 1 , wherein the internal in each of the stripping section and the enrichment section of said continuous multi-stage distillation column B is a tray and/or a packing.

4. The process according to claim 3 , wherein the internal in each of the stripping section and the enrichment section of said continuous multi-stage distillation column B is the tray.

5. The process according to claim 4 , wherein said tray is a sieve tray.

6. The process according to claim 5 , wherein said sieve tray has 150 to 1200 holes/m 2 in a sieve portion thereof, and a cross-sectional area per hole is in a range of from 0.5 to 5 cm 2 .

7. The process according to claim 5 , wherein said sieve tray has 200 to 1100 holes/m 2 in said sieve portion thereof, and the cross-sectional area per hole is in a range of from 0.7 to 4 cm 2 .

8. The process according to claim 5 , wherein said sieve tray has 250 to 1000 holes/m 2 in said sieve portion thereof, and the cross-sectional area per hole is in a range of from 0.9 to 3 cm 2 .

9. The process according to claim 1 , wherein said continuous multi-stage distillation column B has a column bottom temperature in a range of from 150 to 250° C.

10. The process according to claim 1 , wherein said continuous multi-stage distillation column B has a reflux ratio in a range of from 0.5 to 5.

11. The process according to claim 1 , wherein a concentration of the dialkyl carbonate in said column bottom component B B is not less than 97% by weight based on 100% by weight of said column bottom component.

12. The process according to claim 1 , wherein a concentration of the dialkyl carbonate in said column bottom component B B is not less than 99% by weight based on 100% by weight of said column bottom component.

13. The process according to claim 1 , wherein a concentration of the dialkyl carbonate in said column bottom component B B is not less than 99.9% by weight based on 100% by weight of said column bottom component.

14. The process according to claim 1 , wherein said column top component B T is recycled as a starting material for producing the dialkyl carbonate and the diol.

15. The process according to claim 1 , wherein the cyclic carbonate comprises ethylene carbonate and/or propylene carbonate, the aliphatic monohydric alcohol comprises methanol and/or ethanol, and the dialkyl carbonate to be separated out comprises dimethyl carbonate and/or diethyl carbonate.

16. A dialkyl carbonate separated out by the process according to claim 1 , which comprises a halogen content of not more than 0.1 ppm.

17. A dialkyl carbonate separated out by the process according to claim 1 , which comprises a halogen content of not more than 1 ppb.

18. The dialkyl carbonate according to claim 16 , which comprises an aliphatic monohydric alcohol content of not more than 0.1% by weight.

Assignments (2)
MERGER Recorded Jul 13, 2016
From: ASAHI KASEI CHEMICALS
To: ASAHI KASEI KABUSHIKI KAISHA
Reel/Frame 039321/0670 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 25, 2008
From: FUKUOKA, SHINSUKE; MIYAJI, HIRONORI; HACHIYA, HIROSHI; MATSUZAKI, KAZUHIKO
To: ASAHI KASEI CHEMICALS CORPORATION
Reel/Frame 021585/0917 →
Priority Claims (1)
JP 2005-371643 · Dec 26, 2005 · national
Continuity (1)
Related Publication 20090054676A1 · Feb 26, 2009