IP Library Granted Patent US 7,544,350
Granted Patent B2
US 7,544,350 · App. 11/123,925 · Granted Jun 9, 2009

Method of decreasing the UV light degradation of polymers

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Quick Facts
Patent No.
US 7,544,350
App. No.
11/123,925
Granted
Jun 9, 2009
Kind
B2
Abstract

A method of decreasing the UV light degradation of a UV-light degradable polymer comprising adding to said polymer an effective amount of a compound of formula (IX): wherein, R 19 , R 20 and R 21 are the same or different and are selected from the group consisting of C 1 -C 30 alkyl, C 3 -C 8 cycloalkyl, substituted alkyl, substituted cycloalkyl, ester, aryl, heteroaryl, heterocycloalkyl, substituted aryl, substituted heteroaryl, substituted heterocycloalkyl, and amino; R 17 and R 23 are the same or different and are selected from the group consisting of C 1 -C 30 alkyl, C 3 -C 8 cycloalkyl, substituted alkyl, substituted cycloalkyl, ester, aryl, heteroaryl, heterocycloalkyl, substituted aryl, substituted heteroaryl, substituted heterocycloalkyl, cyano, and amino; R 18 and R 22 are the same or different and are selected from the group consisting of substituted diphenylmethylene, unsubstituted diphenylmethylene, substituted 9H-fluorene, and unsubstituted 9H-fluorene; t and u are each in the range of 1 to 100; s is in the range of 0 to 100; and a, b, c, and d are each in the range of 0 to 4.

Claims (13)

1. A method of decreasing the UV light degradation of a UV-light degradable polymer comprising adding to said polymer an effective amount of a compound of formula (IX):

wherein, R 19 , R 20 and R 21 are the same or different and are selected from the group consisting of C 1 -C 30 alkyl, C 3 -C 8 cycloalkyl, substituted alkyl, substituted cycloalkyl, ester, aryl, heteroaryl, heterocycloalkyl, substituted aryl, substituted heteroaryl, substituted heterocycloalkyl, and amino; R 17 and R 23 are the same or different and are selected from the group consisting of C 1 -C 30 alkyl, C 3 -C 8 cycloalkyl, substituted alkyl, substituted cycloalkyl, ester, aryl, heteroaryl, heterocycloalkyl, substituted aryl, substituted heteroaryl, substituted heterocycloalkyl, cyano, and amino; R 18 and R 22 are the same or different and are selected from the group consisting of substituted diphenylmethylene, unsubstituted diphenylmethylene, substituted 9H-fluorene, and unsubstituted 9H-fluorene; t and u are each in the range of 1 to 100; s is in the range of 0 to 100; and a, b, c, and d are each in the range of 0 to 4.

2. The method of claim 1 , wherein R 19 , R 20 and R 21 are selected from the group consisting of C 1 -C 15 branched chain alkyl.

3. The method of claim 1 , wherein R 17 and R 23 are the same and are cyano.

4. The method of claim 1 , wherein said compound of formula (IX) is present in a range of about 0.05% to about 25% by weight of the total weight of the composition.

5. The method of claim 4 , wherein said compound of formula (IX) is present in a range of about 0.1% to about 10% by weight of the total weight of the composition.

6. The method of claim 1 , wherein the effective amount of the compound of formula (IX) is in the range of 0.05% to 25%, based on the total weight of UV light-degradable polymer.

7. The method of claim 1 , wherein the UV light-degradable polymer is PVC.

8. The method of claim 7 , wherein the PVC is in the form of a film.

9. A composition that does not include a dibenzoylmethane compound, comprising a UV light-degradable polymer and 0.05% to 25%, based on the total weight of UV light-degradable polymer, of a compound of formula (IX):

wherein, R 19 , R 20 and R 21 are the same or different and are selected from the group consisting of C 1 -C 30 alkyl, C 3 -C 8 cycloalkyl, substituted alkyl, substituted cycloalkyl, ester, aryl, heteroaryl, heterocycloalkyl, substituted aryl, substituted heteroaryl, substituted heterocycloalkyl, and amino; R 17 and R 23 are the same or different and are selected from the group consisting of C 1 -C 30 alkyl, C 3 -C 8 cycloalkyl, substituted alkyl, substituted cycloalkyl, ester, aryl, heteroaryl, heterocycloalkyl, substituted aryl, substituted heteroaryl, substituted heterocycloalkyl, cyano, and amino; R 18 and R 22 are the same or different and are selected from the group consisting of substituted diphenylmethylene, unsubstituted diphenylmethylene, substituted 9H-fluorene, and unsubstituted 9H-fluorene; t and u are each in the range of 1 to 100; s is in the range of 0 to 100; and a, b, c, and d are each in the range of 0 to 4.

10. The composition of claim 9 , wherein R 19 , R 20 and R 21 are selected from the group consisting of C 1 -C 15 branched chain alkyl.

11. The composition of claim 9 , wherein R 17 and R 23 are the same and are cyano.

Assignments (7)
SECOND AMENDED AND RESTATED INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Nov 25, 2014
From: HALLSTAR INNOVATIONS CORP.
To: BANK OF AMERICA, N.A., AS AGENT
Reel/Frame 034468/0854 →
AMENDED AND RESTATED INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Feb 21, 2012
From: HALLSTAR INNOVATIONS CORP.
To: BANK OF AMERICA, N.A., AS AGENT
Reel/Frame 027742/0917 →
SECURITY INTEREST Recorded Oct 16, 2008
From: HALLSTAR INNOVATIONS CORP.
To: LASALLE BANK NATIONAL ASSOCIATION, AS AGENT
Reel/Frame 021709/0286 →
INTELLECTUAL PROPERTY RELEASE Recorded Oct 14, 2008
From: LASALLE BANK NATIONAL ASSOCIATION, AS AGENT
To: HALLSTAR INNOVATIONS CORP.
Reel/Frame 021669/0701 →
CHANGE OF NAME Recorded May 14, 2007
From: CPH INNOVATIONS CORP.
To: HALLSTAR INNOVATIONS CORP.
Reel/Frame 019287/0001 →
SECURITY AGREEMENT Recorded Jan 25, 2006
From: CPH INNOVATIONS CORP.
To: LASALLE BANK NATIONAL ASSOCIATION, AS AGENT
Reel/Frame 017207/0546 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 16, 2005
From: BONDA, MR. CRAIG A.; O'ROURKE, MR. STEVE; PAVLOVIC, MS. ANNA; SHAH, MR. URVIL B.
To: CPH INNOVATIONS CORP.
Reel/Frame 016165/0413 →