IP Library › Granted Patent US 10,239,822
Granted Patent B2
US 10,239,822 · App. 15/684,740 · Granted Mar 26, 2019

Process for the separation of long chain amino acids and dibasic acids

Inventor: Songzhou Hu (Princeton, NJ)
Assignee: VITAWORKS IP, LLC
C07C227/40B01D3/36B01D9/0004B01D9/0018B01D11/0492C07C51/43C07C51/44C07C51/46C07C51/47C07C51/48C07C209/86C07C227/42
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Quick Facts
Patent No.
US 10,239,822
App. No.
15/684,740
Granted
Mar 26, 2019
Kind
B2
Abstract

There is disclosed a process for the separation of long chain dibasic acid and fatty acid, comprising: (1) reacting a mixture of long chain dibasic acid and fatty acid with ammonium hydroxide to form an insoluble ammonium salt of fatty acid and a soluble ammonium salt of long chain dibasic acid; (2) recovering the insoluble ammonium salt of fatty acid; and (3) adding an acid to the mother liquor of step (2) to obtain the long chain dibasic acid.

Claims (13)

1. A process for the separation of long chain dibasic acid from one or a mixture of two or more fatty acids, comprising:

(1) reacting a mixture of long chain dibasic acid and one or more fatty acids with an aqueous solution of ammonium hydroxide, ammonium bicarbonate, ammonium carbonate, organic amine of the formula NR 1 R 2 R 3 , or a mixture of two or more thereof, to form a suspension of the ammonium salt of fatty acid in a solution of the ammonium salt of long chain dibasic acid, in the absence or presence of solvent;

(2) separating the solid ammonium salt of fatty acid from step (1) by means of solid-liquid separation to provide a mother liquor containing the ammonium salt of long chain dibasic acid;

(3) adding an acid to the mother liquor of step (2) or a solution of the ammonium salt of long chain dibasic acid to yield the long chain dibasic acid; and

(4) recovering the long chain dibasic acid by means of solid-liquid separation or by extraction with an extractant solvent.

2. The process according to claim 1 , wherein R 1 , R 2 , and R 3 of the organic amine NR 1 R 2 R 3 , are each independently hydrogen, C 1 -C 8 alkyl groups, or benzyl group.

3. The process according to claim 1 , wherein the long chain dibasic acid is azelaic acid, sebacic acid, dodecanedioic acid, or brassylic acid.

4. The process according to claim 1 , wherein the fatty acid is stearic acid, palmitic acid, lauric acid, myristic acid, arachidic acid, behenic acid, lignoceric acid, hydroxy stearic acid, keto stearic acid, oxime stearic acid, the Beckmann rearrangement product of oxime fatty acid, or a mixture of two or more thereof.

5. The process according to claim 1 , wherein the solvent is selected from a group consisting of methanol, ethanol, propanol, isopropanol, tert-butanol, tetrahydrofuran, dioxane, or a mixture of two or more thereof.

6. The process according to claim 1 , wherein the acid is selected from a group consisting of hydrochloric acid, hydrobromic acid, hydroiodic acid, sulfuric acid, nitric acid, phosphoric acid, methanesulfonic acid, ethanesulfonic acid, propanesulfonic acid, isethionic acid, benzenesulfonic acid, toluenesulfonic acid, xylenesulfonic acid, sulfamic acid, malic acid, maleic acid, tartaric acid, glycolic acid, lactic acid, citric acid, oxalic acid, formic acid, acetic acid, propionic acid, or a mixture of two or more thereof.

7. The process according to claim 1 , wherein the acid is sulfuric acid.

8. The process according to claim 1 , wherein the extractant solvent is selected from a group consisting of butyl formate, isobutyl formate, butyl acetate, isobutyl acetate, propyl acetate, isopropyl acetate, ethyl acetate, ethyl propionate, octyl acetate, benzene, toluene, xylene, cumene, anisole, diethyl ether, diisopropyl ether, dibutyl ether, methyl tert-butyl ether, ethyl tert-butyl ether, methyl tetrahydrofuran, petroleum ether, cyclohexane, dichloroethane, methylene chloride, chloroform, carbon tetrachloride, trifluoromethylbenzene, n-butanol, isobutanol, amyl alcohol, isoamyl alcohol, hexanol, cyclohexanol, 2-ethylhexanol, isooctanol, sec-octanol, butanone, pentanone, hexanone, cyclohexanone, methyl isobutyl ketone, or a mixture of two or more thereof.

9. The process according to claim 1 , wherein the extractant solvent is toluene.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 26, 2026
From: NATURAMIDE IP LLC
To: SHANGHAI NATURAMIDE NEW MATERIALS CO., LTD.
Reel/Frame 073901/0884 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 24, 2023
From: VITAWORKS IP, LLC
To: NATURAMIDE IP LLC
Reel/Frame 063754/0070 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 28, 2017
From: HU, SONGZHOU
To: VITAWORKS IP, LLC
Reel/Frame 043426/0032 →
Continuity (4)
Continuation In Part 15645899 · Jul 10, 2017
Continuation 15644665 · Jul 7, 2017
Continuation In Part 15635874 · Jun 28, 2017
Related Publication 20190002397A1 · Jan 3, 2019