IP Library Granted Patent US 9,284,244
Granted Patent B2
US 9,284,244 · App. 14/399,339 · Granted Mar 15, 2016

Carboxylic acid salt removal during hydrate inhibitor recovery

Inventor: Salim Deshmukh (Oslo, NO)
Assignee: FJORDS PROCESSING AS
C07C29/88B01D3/34B01D9/0054B01D61/00C07C29/86C07C41/38C07C41/44B01D2311/2642C09K2208/22C10L3/107C10L2290/12
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Quick Facts
Patent No.
US 9,284,244
App. No.
14/399,339
Granted
Mar 15, 2016
Kind
B2
Abstract

A method and system for precipitation and separation of carboxylic acid salts from a hydrate inhibitor solution is disclosed. The method comprises lowering the solubility of the carboxylic acid salts to force precipitation of carboxylic acid salts and separation of the precipitated carboxylic acid salts from the hydrate inhibitor solution.

Claims (14)

1. A method for precipitation and separation of carboxylic acid salts from a hydrate inhibitor fluid stream comprising lowering the solubility of the carboxylic acid salts to force precipitation of carboxylic acid salts and separation of the precipitated carboxylic acid salts by separation of the solid precipitated salts from the hydrate inhibitor solution, wherein the hydrate inhibitor comprises at least one glycol based inhibitor, and wherein the lowering of the solubility is performed by adding an antisolvent to the hydrate inhibitor fluid stream.

2. The method according to claim 1 , wherein the lowering of the solubility is further performed by adding a solution of an inorganic salt comprising divalent cations.

3. The method according to claim 2 , wherein the divalent cations are selected from the group consisting of Ca 2+ , Ba 2+ , Sr 2+ , Mg 2+ , and Fe 2+ .

4. The method according to claim 2 wherein the inorganic salt is BaCl 2 .

5. The method according to claim 1 , wherein the antisolvent is selected from the group consisting of alcohols and ketones.

6. The method according to claim 1 , wherein the antisolvent is selected from the group consisting of butanol, iso-propanol, and acetone.

7. The method according to claim 1 , wherein the hydrate inhibitor is MEG.

8. The method according to claim 1 , wherein the method is performed on a slip stream from a partly lean hydrate inhibitor recycle stream.

9. The method according to claim 1 , wherein the method comprises separation of the added antisolvent after the separation of solids, and where heat is transferred from the remaining partly lean hydrate inhibitor recycle stream to aid the separation of the anti solvent.

10. The method according to claim 1 , wherein the method comprises separation of the added antisolvent after the separation of solids using a membrane separation process.

11. The method according to claim 1 , wherein the method comprises separation of the added antisolvent after the separation of solids using a distillation process.

12. The method according to claim 11 , wherein the method comprises cooling of the antisolvent and reuse of the antisolvent, and wherein the hydrate inhibitor fluid stream is recycled.

13. The method according to claim 1 , wherein the temperature during the precipitation is 0 to 130° C.

14. The method according to claim 1 , wherein the antisolvent is selected from the group consisting of methanol, ethanol, butanol, iso-propanol, and acetone.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 3, 2014
From: DESHMUKH, SALIM
To: FJORDS PROCESSING AS
Reel/Frame 034357/0485 →
Priority Claims (1)
NO 20120547 · May 11, 2012 · national
Continuity (1)
Related Publication 20150119609A1 · Apr 30, 2015