IP Library › Granted Patent US 10,899,700
Granted Patent B2
US 10,899,700 · App. 16/717,165 · Granted Jan 26, 2021

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

Inventors: Songzhou Hu (Princeton, NJ); Zhen Song (Shanghai, CN)
Assignee: Vitaworks IP, LLC
C07C227/40B01D3/36B01D9/0004B01D9/0018B01D9/0059B01D11/0488B01D11/0492C07C51/42C07C51/43C07C51/44C07C51/46C07C51/47C07C51/48C07C209/86C07C227/42B01D21/262
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Quick Facts
Patent No.
US 10,899,700
App. No.
16/717,165
Granted
Jan 26, 2021
Kind
B2
Abstract

There is disclosed a process for the separation of long chain amino acid and long chain dibasic acid, comprising: (1) adding an ammonium salt to the mixture of alkali salts of long chain amino acid and long chain dibasic acid; (2) heating to remove ammonia; and (3) separating long chain amino acid by solid-liquid separation; and (4) acidifying the salt of long chain dibasic acid with an acid to separate long chain dibasic acid.

Claims (17)

1. A process for separation of a long chain amino acid, dibasic acid, short chain alkylamine, and alkanoic acid of the following structures:

from at least two of them in an alkali hydroxide hydrolysis solution of mixed amide derivatives of the following structures:

wherein m is an integer from 0 to 10;

n is an integer from 6 to 20;

X is OR or NR 1 R 2 , wherein OR is OH, C 1 -C 8 monohydric alcohol, or C 1 -C 8 polyhydric alcohol, and R 1 and R 2 are each independently hydrogen or C 1 -C 8 alkyl group; comprising:

(1) adding an ammonium salt to a mixture of alkali salts of a long chain amino acid and a long chain dibasic acid;

(2) heating the solution resulting from step (1) to remove ammonia to yield a crystalline suspension of the long chain amino acid; and

(3) cooling the crystalline suspension and separating the long chain amino acid by a method of solid-liquid separation to obtain a mother liquor containing a salt of the long chain dibasic acid.

2. The process according to claim 1 , wherein the separation of a long chain dibasic acid further comprises:

(4) acidifying the mother liquor of step (3) with an acid to precipitate the long chain dibasic acid; and

(5) recovering the long chain dibasic acid by a method of solid-liquid separation.

3. The process according to claim 1 , wherein the ammonium salt is selected from the group consisting of ammonium chloride, ammonium bromide, ammonium sulfate, ammonium bisulfate, ammonium nitrate, ammonium phosphate, ammonium hydrogen phosphate, ammonium dihydrogen phosphate, ammonium carbonate, ammonium bicarbonate, ammonium sulfite, ammonium bisulfite, ammonium salts of organic carboxylic acids, ammonium salts of aryl sulfonate and alkyl sulfonate, and a mixture of two or more thereof.

4. The process according to claim 1 , wherein the ammonium salt is ammonium sulfate.

5. The process according to claim 2 , wherein the acid is selected from the 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, and a mixture of two or more thereof.

6. The process according to claim 2 , wherein the acid is sulfuric acid.

7. The process according to claim 2 , wherein the long chain dibasic acid is extracted into an extractant solvent after the mother liquor is acidified with the acid.

8. The process according to claim 7 , wherein the extractant solvent is selected from the 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, and trifluoromethylbenzene, n-butanol, isobutanol, amyl alcohol, isoamyl alcohol, hexanol, cyclohexanol, 2-ethylhexanol, isooctanol, sec-octanol, butanone, pentanone, hexanone, cyclohexanone, methyl isobutyl ketone, and a mixture of two or more thereof.

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 Dec 18, 2019
From: HU, SONGZHOU; SONG, ZHEN
To: VITAWORKS IP, LLC
Reel/Frame 051316/0689 →
Continuity (6)
Continuation In Part PCTUS2018039139 · Jun 22, 2018
Continuation 15684740 · Aug 23, 2017
Continuation In Part 15645899 · Jul 10, 2017
Continuation 15644665 · Jul 7, 2017
Continuation In Part 15635874 · Jun 28, 2017
Related Publication 20200157041A1 · May 21, 2020