IP Library Granted Patent US 7,491,838
Granted Patent B2
US 7,491,838 · App. 10/648,572 · Granted Feb 17, 2009

Purification of acetonitrile by a distillative recovery/ion exchange resin treatment process

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Quick Facts
Patent No.
US 7,491,838
App. No.
10/648,572
Granted
Feb 17, 2009
Kind
B2
Abstract

A process of producing HPLC grade acetonitrile (UV cutoff<190) comprising a multistep distillation under reflux conditions followed by acidic ion exchange resin treatment to remove essentially all impurities from the acetonitrile.

Claims (21)

1. A process of producing highly purified acetonitrile having no more than about 0.3 milligrams of acetamide per liter of acetonitrile comprising (1) distilling crude acetonitrile in a first distillation column affixed with a first overhead reflux loop at a first pressure of at least 1 atmosphere to remove HCN, producing a first acetonitrile/water azeotrope and a first bottom product containing water, (2) distilling the first azeotrope in a second distillation column affixed with a second overhead reflux loop at a second pressure less than 1 atmosphere to separate the first azeotrope into a second bottoms product containing water and a second acetonitrile/water azeotrope having a greater acetonitrile concentration than that the first azeotrope, (3) distilling the second acetonitrile/water azeotrope in a third distillation column affixed with a third overhead reflux loop at a third pressure above 1 atmosphere to produce a third acetonitrile/water azeotrope containing substantially all of the water from the second azeotrope, a third bottoms product comprising acetonitrile and heavy organics and a side stream comprising highly pure acetonitrile, and (4) passing the highly pure acetonitrile side stream through an acidic ion exchange resin to further purify said highly pure acetonitrile producing highly purified acetonitrile having a UV cutoff for impurities of <190 nm wherein the reflux ratios in Steps 1, 2 and 3 are kept at greater than 3 to 1, greater than 3.4 to 1 and greater than 6.4 to 1, respectively.

2. The process of claim 1 wherein the reflux ratio in step 1 is greater than about 4.4:1.

3. The process of claim 2 wherein the reflux ratio in step 2 is greater than about 4.5:1.

4. The process of claim 3 wherein the reflux ratio in step 3 is greater than about 8:1.

5. The process of claim 1 wherein the acidic ion exchange resin is selected to include a strong acid incorporating sulfonic acid functional groups.

6. The process of claim 1 wherein the acidic ion exchange resin is selected to include weak acid resin incorporating carboxylic acid functional groups.

7. The process of claim 1 further comprising distilling the purified acetonitrile recovered from the acidic ion exchange resin.

8. The process of claim 7 wherein the reflux ratio in step 1 is greater than about 4.4:1.

9. The process of claim 8 wherein the reflux ratio in step 2 is greater than about 4.5:1.

10. The process of claim 9 wherein the reflux ratio in step 3 is greater than about 8:1.

11. The process of claim 7 wherein the acidic ion exchange resin is selected to include a strong acid incorporating sulfonic acid functional groups.

12. The process of claim 7 wherein the acidic ion exchange resin is selected to include weak acid resin incorporating carboxylic acid function groups.

13. A process of producing highly purified acetonitrile comprising:

distilling crude acetonitrile in a first distillation column affixed with a first overhead reflux loop operating at a reflux ratio of greater than 3 to 1 and at a first pressure of at least 1 atmosphere for removing HCN to produce a first acetonitrile/water azeotrope and a first bottom product containing water;

distilling the first azeotrope in a second distillation column affixed with a second overhead reflux loop operating at a reflux ratio of greater than 3.4 to 1 and at a second pressure less than 1 atmosphere to separate the first azeotrope into a second bottoms product containing water and a second acetonitrile/water azeotrope having a greater acetonitrile concentration than that of the first azeotrope;

distilling the second acetonitrile/water azeotrope in a third distillation column affixed with a third overhead reflux loop operating at a reflux ratio of greater than 6.4 to 1 and at a third pressure above 1 atmosphere to produce a third acetonitrile/water azeotrope containing substantially all of the water from the second azeotrope, a third bottoms product comprising acetonitrile and heavy organics, and a side stream comprising highly pure acetonitrile; and

passing the highly pure acetonitrile side stream through an acidic ion exchange resin to further purify the highly pure acetonitrile producing highly purified acetonitrile having an assay of at least 99.97% acetonitrile.

14. The process of claim 13 wherein the reflux ratio of the first overhead reflux loop is greater than about 4.4:1; the reflux ratio in the second overhead reflux loop is greater than about 4.5:1; and the reflux ratio in the third overhead reflux loop is greater than about 8:1.

15. The process of claim 13 wherein the acidic ion exchange resin is selected to include a strong acid incorporating sulfonic acid functional groups.

16. The process of claim 13 wherein the acidic ion exchange resin is selected to include weak acid resin incorporating carboxylic acid functional groups.

17. The process of claim 13 further comprising distilling the purified acetonitrile recovered from the acidic ion exchange resin.

Assignments (6)
SECURITY AGREEMENT Recorded Jun 27, 2012
From: INEOS USA LLC
To: BARCLAYS BANK PLC
Reel/Frame 028451/0309 →
SECURITY INTEREST Recorded Jul 2, 2010
From: INEOS USA LLC
To: BARCLAYS BANK PLC (IN ITS CAPACITY AS SECURITY TRUSTEE FOR ITSELF AND OTHER SECURED PARTIES)
Reel/Frame 024651/0047 →
SECURITY AGREEMENT Recorded Feb 7, 2007
From: INEOS USA LLC
To: BARCLAYS BANK PLC
Reel/Frame 018866/0369 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 25, 2007
From: STANDARD OIL COMPANY, THE
To: O&D USA LLC
Reel/Frame 018806/0941 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 25, 2007
From: O&D USA-LC
To: INNOVENE USA LLC
Reel/Frame 018816/0199 →
CHANGE OF NAME Recorded Jan 25, 2007
From: INNOVENE USA LLC
To: INEOS USA LLC
Reel/Frame 018826/0918 →