IP Library Patent Application 13728067
Patent Application
App. No. 13/728,067

Rosin Esters for Non-Woven Applications, Methods of Making and Using and Products Therefrom

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Quick Facts
Patent No.
US None
App. No.
13/728,067
Filed
Dec 27, 2012
Art Unit
1767
USPC
530/218
Abstract

Rosin esters having suitable color, color stability and/or odor to make them useful for non-woven applications, to non-woven products made from and/or comprising rosin esters, and to methods of making and using such rosin esters and products.

Claims (25)

1 . A method of producing a rosin ester, the method comprising:

(A) Contacting a rosin having PAN isomers with disproportionation agent to provide a rosin having a PAN number less than 45 providing a disproportionated rosin;

(B) Contacting the disproportionated rosin with an adduction agent to further reduce the PAN number to provide an adducted rosin;

(C) Contacting the adducted rosin with a polyhydric polyol to form a rosin ester.

2 . The method of claim 1 , wherein the disproportationation agent comprises at least one selected from among phenol sulfides, metals, iodine, iodides, and sulfides, and the adduction agent is selected to react with the PAN isomers of the rosin through a Diels-Alder reaction or an Ene reaction.

3 . The method of claim 1 wherein the disproportationation agent comprises at least one selected from 2,2′-thiobis phenols, 3,3′-thiobisphenols, 4,4′-thiobis(resorcinol) and t,t′-thiobis(pyrogallol), 4,4′-thiobis(6-t-butyl-m-cresol) and 4/4′-thiobis(6-t-butyl-o-cresol) thiobisnaphthols, 2,2′-thio-bisphenols, 3,3′-thio-bis phenols, palladium, nickel, platinum, iodine, iron iodide, iron sulfide.

4 . The method of claim 1 , wherein the adduction agent comprises at least one selected from fumaric acid, maleic anhydride, acrylic acid, unsaturated acids and anhydrides.

5 . The method of claim 1 , wherein the polyhydric polyol comprises less than 20 weight percent pentaerythritol.

6 . The method of claim 5 , wherein the polyhydric polyol comprises at least one selected from the group consisting of ethylene glycol, propylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol, trimethylene glycol, glycerol, pentaerythritol, dipentaerythritol, tripentaerythritol, trimethylolethane, trimethylolpropane, mannitol and sorbitol.

7 . The method of claim 5 , wherein the polyhydric alcohol comprises at least one selected from the group consisting of glycerol and trimethylolpropane.

8 . The method of claim 1 , wherein the rosin ester has an odor intensity of less than 80% relative to comparison rosin ester made from 100% pentaerythritol.

9 . A method of producing a rosin ester, the method comprising:

(A) Contacting rosin having a PAN number less than 45 with an adduction agent to further reduce the PAN number to provide an adducted rosin;

(B) Contacting the adducted rosin with a polyhydric polyol to form a rosin ester.

10 . The method of claim 9 , wherein the adduction agent is selected to react with the PAN isomers of the rosin through a Diels-Alder reaction or an Ene reaction.

11 . The method of claim 9 , wherein the adduction agent comprises at least one selected from fumaric acid, maleic anhydride, acrylic acid, unsaturated acids and anhydrides.

12 . The method of claim 9 , wherein the polyhydric polyol comprises less than 20 weight percent pentaerythritol.

13 . The method of claim 12 , wherein the polyhydric polyol comprises at least one selected from the group consisting of ethylene glycol, propylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol, trimethylene glycol, glycerol, pentaerythritol, dipentaerythritol, tripentaerythritol, trimethylolethane, trimethylolpropane, mannitol and sorbitol.

14 . The method of claim 12 , wherein the polyhydric alcohol comprises at least one selected from the group consisting of glycerol and trimethylolpropane.

15 . The method of claim 9 , wherein the rosin ester has an odor intensity of less than 80%relative to comparison rosin ester made from 100% pentaerythritol.

16 . A rosin ester composition having an odor intensity of less than 80% relative to comparison rosin ester made from 100% pentaerythritol.

17 . The composition of claim 16 having an odor intensity of less than 60% relative to comparison rosin ester made from 100% pentaerythritol.

18 . The composition of claim 16 having an odor intensity of less than 55% relative to comparison rosin ester made from 100% pentaerythritol.

19 . The composition of claim 16 having an odor intensity of less than 50% relative to comparison rosin ester made from 100% pentaerythritol.

20 - 27 . (canceled)

Assignments (9)
CORRECTIVE ASSIGNMENT TO CORRECT THE PATENT NO. 8837224 TO PATENT NO. 7737224 PREVIOUSLY RECORDED AT REEL: 037448 FRAME: 0453. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Jun 11, 2022
From: KRATON POLYMERS U.S. LLC; ARIZONA CHEMICAL COMPANY, LLC
To: BANK OF AMERICA, N.A.
Reel/Frame 060344/0919 →
RELEASE OF SECURITY INTEREST Recorded Mar 15, 2022
From: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH, AS COLLATERAL AGENT
To: ARIZONA CHEMICAL COMPANY, LLC
Reel/Frame 059366/0727 →
PATENT SECURITY AGREEMENT Recorded Jan 7, 2016
From: ARIZONA CHEMICAL COMPANY, LLC
To: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH, AS COLLATERAL AGENT
Reel/Frame 037457/0928 →
RELEASE OF SECURITY INTEREST IN INTELLECTUAL PROPERTY COLLATERAL AT REEL/FRAME NO. 33146/0361 Recorded Jan 6, 2016
From: GOLDMAN SACHS BANK USA
To: ARIZONA CHEMICAL COMPANY LLC
Reel/Frame 037451/0169 →
CORRECTIVE ASSIGNMENT TO CORRECT THE PATENT NUMBER 8837224 TO PATENT NUMBER 7737224 PREVIOUSLY RECORDED AT REEL: 037448 FRAME: 0453. ASSIGNOR(S) HEREBY CONFIRMS THE SECURITY INTEREST. Recorded Jan 6, 2016
From: KRATON POLYMERS U.S. LLC; ARIZONA CHEMICAL COMPANY, LLC
To: BANK OF AMERICA, N.A.
Reel/Frame 037448/0453 →
RELEASE OF SECURITY INTEREST IN PATENT RIGHTS Recorded Jan 6, 2016
From: ANTARES CAPITAL LP, AS SUCCESSOR TO GENERAL ELECTRIC CAPITAL CORPORATION
To: ARIZONA CHEMICAL COMPANY LLC
Reel/Frame 037451/0057 →
ASSIGNMENT OF INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Oct 9, 2015
From: GENERAL ELECTRIC CAPITAL CORPORATION, AS RETIRING AGENT
To: ANTARES CAPITAL LP, AS SUCCESSOR AGENT
Reel/Frame 036827/0443 →
SECURITY INTEREST Recorded Jun 12, 2014
From: ARIZONA CHEMICAL COMPANY LLC
To: GENERAL ELECTRIC CAPITAL CORPORATION, AS FIRST LIEN COLLATERAL AGENT
Reel/Frame 033146/0333 →
SECURITY INTEREST Recorded Jun 12, 2014
From: ARIZONA CHEMICAL COMPANY LLC
To: GOLDMAN SACHS BANK USA, AS SECOND LIEN COLLATERAL AGENT
Reel/Frame 033146/0361 →