IP Library Granted Patent US 7,012,118
Granted Patent B2
US 7,012,118 · App. 10/681,608 · Granted Mar 14, 2006

Photopolymerizable compositions and flexographic plates prepared from controlled distribution block copolymers

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Quick Facts
Patent No.
US 7,012,118
App. No.
10/681,608
Granted
Mar 14, 2006
Kind
B2
Abstract

The present invention relates to a photopolymerizable composition, which comprises: (a) a block copolymer component comprising an unhydrogenated styrene diene block copolymer and a hydrogenated controlled distribution styrene diene block copolymer (b) one or more photopolymerizable ethylenically unsaturated low molecular weight compounds, (c) one or more polymerization initiators, and optionally (d) from 0 to 40% by weight, based on the total photopolymerizable compositions, of one or more auxiliaries. The invention also includes flexographic printing plates derived from said photopolymerizable compositions, and flexographic printing relief forms prepared from said plates.

Claims (41)

1. A photopolymerizable composition, which comprises:

a. a block copolymer component comprising a non-hydrogenated styrene/diene block copolymer and a hydrogenated, controlled-distribution block copolymer, wherein said hydrogenated, controlled-distribution block copolymer has at least one polymer block A and at least one polymer block B, and wherein:

i) prior to hydrogenation each A block is a mono alkenyl arene homopolymer block and each B block is a controlled distribution copolymer block of at least one conjugated diene and at least one mono alkenyl arene;

ii) subsequent to hydrogenation about 0–10% of the arene double bonds have been reduced, and at least about 90% of the conjugated diene double bonds have been reduced;

iii) each A block having a number average molecular weight between about 3,000 and about 60,000 and each B block having a number average molecular weight between about 20,000 and about 300,000;

iv) each B block comprises terminal regions adjacent to the A blocks that are rich in conjugated diene units and one or more regions not adjacent to the A blocks that are rich in mono alkenyl arene units;

v) the total amount of mono alkenyl arene in the hydrogenated block copolymer is about 20 percent weight to about 80 percent weight; and

vi) the weight percent of mono alkenyl arene in each B block is between about 10 percent and about 75 percent;

vii) the B block has a monoalkenyl arene blockiness index of less than about 40%;

b one or more photopolymerizable ethylenically unsaturated low molecular weight compounds,

c one or more polymerization initiators, and optionally

d from 0 to 40% by weight, based on the total photopolymerizable composition, of one or more auxiliaries.

2. The photopolymerizable composition according to claim 1 wherein said mono alkenyl arene is styrene and said conjugated diene in said controlled distribution block copolymer is selected from the group consisting of isoprene and butadiene.

3. The photopolymerizable composition according to claim 2 wherein said conjugated diene is butadiene, and wherein about 20 to about 80 mol percent of the condensed butadiene units in block B have 1,2-configuration.

4. The photopolymerizable composition according to claim 3 wherein the styrene blockiness of the block B is less than about 40 percent.

5. The photopolymerizable composition according to claim 3 wherein the weight percent of styrene in each B block is between about 10 percent and about 30 percent, and the styrene blockiness index of each block B is less than about 10 percent, said styrene blockiness index being defined to be the proportion of styrene units in the block B having two styrene neighbors on the polymer chain.

6. The photopolymerizable composition according to claim 3 wherein said hydrogenated, controlled-distribution block copolymer is an ABA, (A-B) n , (A-B) n A, or (A-B) n X block copolymer where n is an integer from 2 to about 30, X is the coupling agent residue, said block copolymer having a total molecular weight of about 40,000 to about 140,000 and wherein each B block has between 10 and 30 weight percent styrene.

7. The photopolymerizable composition according to claim 3 , wherein component (b) is selected from esters or amides of acrylic acid or methacrylic acid with monofunctional or polyfunctional alcohols, amines, aminoalcohols and hydroxyl ethers or hydroxyl esters.

8. The photopolymerizable composition according to claim 7 , wherein component (b) is selected from butyl acrylate, isodecyl acrylate, trimethylolpropane triacrylate, hexane diol diacrylate and dipentaerythritol monohydroxypentacrylate.

9. The photopolymerizable composition of claim 8 wherein component (b) is hexane diol diacrylate.

10. The photopolymerizable composition of claim 3 wherein the weight ratio of controlled distribution block copolymer to unhydrogenated styrene/diene block copolymer is between about 5:95 to about 40:60.

11. The photopolymerizable composition of claim 10 wherein said unhydrogenated styrene/diene block copolymer is an CDC, (C-D) n , (C-D) n C, (C-D) n Y(D) m or (C-D) n Y block copolymer where n is an integer from 2 to about 30, m is an integer from 1 to about 5, Y is the coupling agent residue, C is a styrene homopolymer block, and D is a polymer block of one or more conjugated dienes selected from butadiene and isoprene, said unhydrogenated block copolymer having a total molecular weight of about 40,000 to about 200,000.

12. The photopolymerizable composition according to claim 11 wherein said unhydrogenated block copolymer is a styrene-isoprene-styrene block copolymer.

13. The photopolymerizable composition according to claim 11 wherein said unhydrogenated block copolymer is a styrene-isoprene/butadiene-styrene block copolymer.

14. The photopolymerizable composition according to claim 11 wherein said unhydrogenated block copolymer is a radial styrene/butadiene block copolymer having the structure (C-D) n Y or (C-D) n Y(D) m where the C block is a block of styrene polymer, the D block is a butadiene block, Y is the coupling agent residue, n is on average about 2 and m is on average about 1.5.

15. The photopolymerizable composition of claim 3 wherein said polymerization initiators are selected from the group consisting of methylbenzoin, benzoin acetate, benzophenone, benzyl dimethyl-ketal and ethyl anthraquinone/4,4-bis(dimethyl amino)benzo-phenone.

16. The photopolymerizable composition of claim 3 wherein said auxiliaries are selected from the group consisting of plasticizers, aromatic resins, compatible rubbers, fillers, dyes, pigments, antioxidants, antiozonates, and thermal polymerization inhibitors.

17. A flexographic printing plate derived from the photopolymerizable composition of claim 1 .

18. A flexographic printing relief form prepared from the flexographic printing plate of claim 17 .

19. A clear composition comprising:

b. about 5 to about 75 weight percent of a hydrogenated controlled distribution block copolymer, and

c. about 95 to about 25 weight percent of an unhydrogenated radial styrene butadiene block copolymer, wherein said controlled distribution block copolymer has at least one polymer block A and at least one polymer block B, and wherein:

viii) prior to hydrogenation each A block is a mono alkenyl arene homopolymer block and each B block is a controlled distribution copolymer block of at least one conjugated diene and at least one mono alkenyl arene;

ix) subsequent to hydrogenation about 0–10% of the arene double bonds have been reduced, and at least about 90% of the conjugated diene double bonds have been reduced;

x) each A block having a number average molecular weight between about 3,000 and about 60,000 and each B block having a number average molecular weight between about 20,000 and about 300,000;

xi) each B block comprises terminal regions adjacent to the A blocks that are rich in conjugated diene units and one or more regions not adjacent to the A blocks that are rich in mono alkenyl arene units;

xii) the total amount of mono alkenyl arene in the hydrogenated block copolymer is about 20 percent weight to about 80 percent weight; and

xiii) the weight percent of mono alkenyl arene in each B block is between about 10 percent and about 75 percent;

xiv) the B block has a monoalkenyl axene blockiness index of less than about 40%;

and the unhydrogenated radial block copolymer is a radial styrene/butadiene block copolymer having the structure (C-D) n Y(D) m where the C block is a polymer block of styrene, the D block is a polymer block of 1,3-butadiene having a 1,2-vinyl content of between about 5 mol percent and 80 mol percent, Y is the coupling agent residue, n is an integer from 2 to about 30 and m is an integer from 1 to about 10.

20. The composition according to claim 19 wherein said controlled distribution block copolymer is an ABA, (A-B) n , (A-B) n A, or (A-B) n X block copolymer where n is an integer from 2 to about 30, X is the coupling agent residue, and wherein said monoalkenyl arene is styrene and said conjugated diene is 1,3-butadiene.

Assignments (15)
RELEASE OF SECURITY INTEREST IN PATENTS Recorded Jul 24, 2024
From: GOLDMAN SACHS BANK USA, AS COLLATERAL AGENT
To: KRATON CHEMICAL, LLC; KRATON CORPORATION
Reel/Frame 068671/0836 →
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 →
SECURITY INTEREST Recorded Mar 18, 2022
From: KRATON CHEMICAL, LLC; KRATON POLYMERS LLC; KRATON POLYMERS U.S. LLC
To: GOLDMAN SACHS BANK USA, AS COLLATERAL AGENT
Reel/Frame 059864/0455 →
SECURITY INTEREST Recorded Mar 18, 2022
From: KRATON CHEMICAL, LLC; KRATON POLYMERS LLC; KRATON POLYMERS U.S. LLC
To: GOLDMAN SACHS BANK USA, AS COLLATERAL AGENT
Reel/Frame 059525/0804 →
RELEASE OF SECURITY INTEREST Recorded Mar 16, 2022
From: BANK OF AMERICA, N.A.
To: KRATON POLYMERS U.S. LLC; KRATON CHEMICAL, LLC F/K/A ARIZONA CHEMICAL COMPANY, LLC; KRATON POLYMERS LLC; KRATON CORPORATION; KRATON CHEMICAL B.V.
Reel/Frame 059910/0017 →
RELEASE OF SECURITY INTEREST Recorded Mar 15, 2022
From: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH, AS COLLATERAL AGENT
To: KRATON POLYMERS U.S. LLC
Reel/Frame 059366/0611 →
SECURITY INTEREST Recorded Apr 16, 2020
From: KRATON POLYMERS U.S. LLC; KRATON CHEMICAL, LLC F/K/A ARIZONA CHEMICAL COMPANY, LLC; KRATON POLYMERS LLC; KRATON CORPORATION
To: BANK OF AMERICA, N.A.
Reel/Frame 053020/0101 →
PATENT SECURITY AGREEMENT Recorded Jan 7, 2016
From: KRATON POLYMERS U.S. LLC
To: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH, AS COLLATERAL AGENT
Reel/Frame 037457/0843 →
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 →
CORRECTIVE ASSIGNMENT TO CORRECT THE INCORRECT PATENT NUMBER 7720798 AND REPLACE WITH PATENT NUMBER 7220798 PREVIOUSLY RECORDED ON REEL 025845 FRAME 0795. ASSIGNOR(S) HEREBY CONFIRMS THE RELEASE BY SECURED PARTY. Recorded Dec 16, 2015
From: USB AG, STAMFORD BRANCH
To: KRATON POLYMERS U.S. LLC
Reel/Frame 037312/0070 →
RELEASE OF SECURITY INTEREST Recorded Mar 28, 2013
From: BANK OF AMERICA, N.A.
To: KRATON POLYMERS U.S. LLC
Reel/Frame 030108/0288 →
NOTICE OF GRANT OF SECURITY INTEREST IN PATENTS Recorded Mar 4, 2011
From: KRATON POLYMERS U.S. LLC
To: BANK OF AMERICA N.A., AS COLLATERAL AGENT
Reel/Frame 025899/0176 →
RELEASE OF SECURITY INTEREST Recorded Feb 24, 2011
From: UBS AG, STAMFORD BRANCH
To: KRATON POLYMERS U.S. LLC
Reel/Frame 025845/0795 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 29, 2006
From: HANSEN, DAVID ROMME; ST. CLAIR, DAVID JOHN; DUBOIS, DONN ANTHONY; HANDLIN, JR., DALE L.; WILLIS, CARL L.
To: KRATON POLYMES U.S. LLC
Reel/Frame 018348/0250 →
SECURITY INTEREST Recorded Jan 2, 2004
From: KRATON POLYMERS U.S. LLC
To: UBS AG, STAMFORD BRANCH
Reel/Frame 014242/0281 →