IP Library Patent Application 15787300
Patent Application
App. No. 15/787,300

Renewably Derived Polyamides and Methods of Making the Same

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Patent No.
US None
App. No.
15/787,300
Abstract

Methods of making polyamides from renewable materials, such as natural oils, are generally disclosed herein. In some embodiments, the polyamides are nylon-10. In some such embodiments, nylon-10 is made by polymerizing 10-aminodecanoic acid, or esters thereof. In some further such embodiments, the 10-aminodecanoic acid monomers (or esters thereof) are derived from natural oils via the metathesis of unsaturated fatty acid moieties of the natural oil.

Claims (34)

1 . A method of making a polyamide from a natural oil, the method comprising:

providing 9-decenoic acid, wherein providing 9-decenoic acid comprises deriving 9-decenoic acid from a natural oil composition;

reacting 9-decenoic acid with a brominating agent to form 10-bromodecanoic acid;

reacting 10-bromodecanoic acid with an aminating agent to form 10-aminodecanoic acid; and

polymerizing 10-aminodecanoic acid to form a polyamide-10 polymer.

2 . The method of claim 1 , wherein deriving 9-decenoic acid from a natural oil comprises:

providing a natural oil composition comprising unsaturated natural fatty acid esters;

reacting the unsaturated natural fatty acid esters with a short-chain alpha-olefin in the presence of a metathesis catalyst to form 9-decenoic acid esters and 1-decene; and

converting the 9-decenoic acid esters to 9-decenoic acid.

3 . The method of claim 2 , wherein the unsaturated natural fatty acid esters are C 1-8 alkyl esters of unsaturated natural fatty acids, and wherein the 9-decenoic acid esters are C 1-8 alkyl esters of 9-decenoic acid.

4 . The method of claim 3 , wherein the unsaturated natural fatty acid esters are methyl esters of unsaturated natural fatty acids, and wherein the 9-decenoic acid esters are methyl esters of 9-decenoic acid.

5 . The method of claim 2 , wherein the unsaturated natural fatty acid esters are glyceryl esters of unsaturated natural fatty acids, and wherein the 9-decenoic acid esters are glyceryl esters of 9-decenoic acid.

6 . The method of claim 2 , wherein the unsaturated natural fatty acids are selected from the group consisting of myristoleic acid, palmitoleic acid, oleic acid, elaidic acid, linoleic acid, linoelaidic acid, and α-linolenic acid.

7 . The method of claim 6 , wherein the unsaturated natural fatty acids are selected from the group consisting of oleic acid, linoleic acid, and α-linolenic acid.

8 . The method of claim 2 , wherein converting the 9-decenoic acid esters to 9-decenoic acid comprises hydrolyzing the 9-decenoic acid esters to form 9-decenoic acid.

9 . The method of claim 2 , wherein converting the 9-decenoic acid esters to 9-decenoic acid comprises:

saponifying the 9-decenoic acid esters to form 9-decenoate anions; and

acidifying the 9-decenoate anions to form 9-decenoic acid.

10 . The method of claim 5 , wherein converting the 9-decenoic acid esters to 9-decenoic acid comprises:

reacting the glyceryl esters of 9-decenoic acid with a C 1-8 monohydric alkanol to form C 1-8 esters of 9-decenoic acid; and

converting the C 1-8 esters of 9-decenoic acid to 9-decenoic acid.

11 . The method of claim 10 , wherein the C 1-8 monohydric alkanol is selected from the group consisting of: methanol, ethanol, propanol, isopropanol, butanol, sec-butanol, tert-butanol, pentanol, neopentanol, hexanol, heptanol, octanol, and 2-ethylhexanol.

12 . The method of claim 11 , wherein the C 1-8 monohydric alkanol is methanol.

13 . The method of claim 10 , wherein the unsaturated natural fatty acids are selected from the group consisting of myristoleic acid, palmitoleic acid, oleic acid, elaidic acid, linoleic acid, linoelaidic acid, and α-linolenic acid.

14 . The method of claim 13 , wherein the unsaturated natural fatty acids are selected from the group consisting of oleic acid, linoleic acid, and α-linolenic acid.

15 . The method of claim 10 , wherein converting the C 1-8 esters of 9-decenoic acid to 9-decenoic acid comprises hydrolyzing the C 1-8 esters of 9-decenoic acid to form 9-decenoic acid.

16 . The method of claim 10 , wherein converting the C 1-8 esters of 9-decenoic acid to 9-decenoic acid comprises:

saponifying the C 1-8 esters of 9-decenoic acid to form 9-decenoate anions; and

acidifying the 9-decenoate anions to form 9-decenoic acid.

17 . The method of claim 2 , wherein the short-chain alpha olefin is selected from the group consisting of: ethylene, propylene, 1-butene, isobutene, 1-pentene, 1-hexene, 1-heptene, 1-octene, and 1-nonene.

18 . The method of claim 17 , wherein the short-chain alpha olefin is selected from the group consisting of: ethylene, propylene, and 1-butene.

19 . The method of claim 1 , wherein the brominating agent is hydrobromic acid.

20 . The method of claim 1 , wherein the aminating agent is ammonia.

21 - 55 . (canceled)

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 15, 2020
From: ELEVANCE RENEWABLE SCIENCES, INC.
To: WILMAR TRADING PTE LTD
Reel/Frame 052942/0933 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 19, 2020
From: QUINN, JORDAN R.
To: ELEVANCE RENEWABLE SCIENCES, INC.
Reel/Frame 052159/0229 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 9, 2019
From: BERTIN, PAUL A.
To: ELEVANCE RENEWABLE SCIENCES, INC.
Reel/Frame 049132/0906 →