IP Library Granted Patent US 10,597,481
Granted Patent B2
US 10,597,481 · App. 15/548,640 · Granted Mar 24, 2020

Hydrogenated block copolymer

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Quick Facts
Patent No.
US 10,597,481
App. No.
15/548,640
Granted
Mar 24, 2020
Kind
B2
Abstract

A hydrogenated block copolymer prepared by hydrogenating a block copolymer that contains a polymer block (A) containing a structural unit derived from an aromatic vinyl compound, a polymer block (B) containing a structural unit derived from farnesene, and a polymer block (C) containing a structural unit derived from a conjugated diene except farnesene, wherein the block copolymer contains at least two above polymer blocks (A), at least one above polymer block (B) and at least one above polymer block (C), and wherein at least one above polymer block (B) is at the terminal, and the hydrogenation rate of the carbon-carbon double bond in the polymer block (B) and the polymer block (C) is 50 mol % or more.

Claims (31)

1. A hydrogenated block copolymer prepared by hydrogenating a block copolymer that comprises a polymer block (A) comprising a structural unit derived from an aromatic vinyl compound, a polymer block (B) comprising a structural unit derived from farnesene, and a polymer block (C) comprising a structural unit derived from a conjugated diene other than farnesene,

wherein:

the block copolymer comprises at least two of the polymer blocks (A), at least one of the polymer block (B) and at least one of the polymer block (C), and wherein at least one of the polymer block (B) is at a terminal,

50 mol % or more of a total of carbon-carbon double bonds in the at least one polymer block (B) and in the at least one polymer block (C) are hydrogenated,

the hydrogenated block copolymer comprises a structure that comprises the polymer block (B), the polymer block (A), and the polymer block (C), in that order, and

an order-disorder transition temperature (ODT) of the hydrogenated block copolymer, as measured by dynamic viscoelastometry, is 290° C. or lower.

2. The hydrogenated block copolymer according to claim 1 , wherein 70 mol % or more of the total of the carbon-carbon double bonds in the at least one polymer block (B) are hydrogenated.

3. The hydrogenated block copolymer according to claim 1 , wherein a ratio by mass of the at least two polymer blocks (A) to a total mass of the at least two polymer blocks (A), the at least one polymer block (B) and the at least one polymer block (C) is from 5/100 to 80/100.

4. The hydrogenated block copolymer according to claim 1 , wherein the aromatic vinyl compound is at least one selected from the group consisting of styrene, a-methylstyrene and 4-methylstyrene.

5. The hydrogenated block copolymer according to claim 1 , wherein the conjugated diene other than farnesene is at least one selected from the group consisting of butadiene, isoprene and myrcene.

6. The hydrogenated block copolymer according to claim 1 , wherein a ratio by mass of the at least one polymer block (C) to the at least one polymer block (B) is from 5/95 to 95/5.

7. The hydrogenated block copolymer according to claim 1 , wherein a peak top molecular weight of the at least two polymer blocks (A) is from 2,000 to 100,000, a peak top molecular weight of the at least one polymer block (B) is from 2,000 to 200,000, and a peak top molecular weight of the at least one polymer block (C) is from 4,000 to 200,000.

8. The hydrogenated block copolymer according to claim 1 , wherein the ODT of the hydrogenated block copolymer, as measured by dynamic viscoelastometry, is 260° C. or lower.

9. A method for producing the hydrogenated block copolymer of claim 1 , comprising:

producing the at least one polymer block (B), the at least two polymer blocks (A) and the at least one polymer block (C) in that order to give a resultant block copolymer, and

hydrogenating the resultant block copolymer.

10. A hydrogenated block copolymer composition comprising the hydrogenated block copolymer of claim 1 , and at least one selected from the group consisting of a polyolefin resin, a tackifier resin and a softening agent.

11. A molded article comprising the hydrogenated block copolymer of claim 1 .

12. A laminate comprising a layer comprising the hydrogenated block copolymer of claim 1 .

13. A film comprising the hydrogenated block copolymer of claim 1 .

14. A protective film comprising the laminate of claim 12 .

15. A fiber comprising the hydrogenated block copolymer of claim 1 .

16. A nonwoven fabric comprising the hydrogenated block copolymer of claim 1 .

17. A decorative molding material comprising the laminate of claim 12 .

18. An adhesive comprising the hydrogenated block copolymer of claim 1 .

19. A hydrogenated block copolymer prepared by hydrogenating a block copolymer that comprises a polymer block (A) comprising a structural unit derived from an aromatic vinyl compound, a polymer block (B) comprising a structural unit derived from farnesene, and a polymer block (C) comprising a structural unit derived from a conjugated diene other than farnesene,

wherein:

the block copolymer comprises at least two of the polymer blocks (A), at least one of the polymer block (B) and at least one of the polymer block (C), and wherein at least one of the polymer block (B) is at a terminal,

50 mol % or more of a total of carbon-carbon double bonds in the at least one polymer block (B) and in the at least one polymer block (C) are hydrogenated,

the hydrogenated block copolymer comprises a structure that comprises the polymer block (B), the polymer block (A), and the polymer block (C), in that order, and

a peak top molecular weight of the at least two polymer block blocks (A) is from 2,000 to 100,000, a peak top molecular weight of the at least one polymer block (B) is from 2,000 to 200,000, and a peak top molecular weight of the at least one polymer block (C) is from 4,000 to 200,000.

Assignments (9)
SECURITY INTEREST Recorded May 24, 2024
From: AMYRIS, INC.
To: EUAGORE, LLC
Reel/Frame 067528/0467 →
SECURITY INTEREST Recorded Aug 17, 2023
From: AMYRIS, INC.; AMYRIS CLEAN BEAUTY, INC.; AMYRIS FUELS, LLC; AB TECHNOLOGIES LLC; APRINNOVA, LLC; AMYRIS-OLINKA, LLC; ONDA BEAUTY INC.; UPLAND 1 LLC; AMYRIS ECO-FAB LLC; CLEAN BEAUTY 4U HOLDINGS, LLC; AMYRIS CLEAN BEAUTY LATAM LTDA; INTERFACES INDUSTRIA E COMERCIA DE COSMETICOS LTDA; AMYRIS BIOTECHNOLOGIA DO BRASIL LTDA; AMYRIS EUROPE TRADING B.V. (NETHERLANDS); AMYRIS BIO PRODCUTS PORTUGAL, UNIPESSOAL, LDA; BEAUTY LABS INTERNATIONAL LIMITED; AMYRIS UK TRADING LIMITED
To: EUAGORE, LLC
Reel/Frame 064619/0778 →
SECURITY INTEREST Recorded Aug 3, 2023
From: AMYRIS CLEAN BEAUTY, INC.; AMYRIS FUELS, LLC; AB TECHNOLOGIES LLC; AMYRIS, INC.
To: MUIRISC, LLC
Reel/Frame 064492/0518 →
RELEASE OF SECURITY INTEREST Recorded Feb 14, 2023
From: SCHOTTENFELD OPPORTUNITIES FUND II, L.P.
To: AMYRIS, INC.
Reel/Frame 062760/0818 →
RELEASE OF SECURITY INTEREST Recorded Feb 14, 2023
From: NAXYRIS S.A.
To: AMYRIS, INC.
Reel/Frame 062760/0753 →
SECURITY INTEREST Recorded Oct 18, 2022
From: AMYRIS, INC.
To: FORIS VENTURES, LLC
Reel/Frame 061703/0499 →
GRANT OF PATENT SECURITY INTEREST Recorded Nov 20, 2019
From: AMYRIS, INC.
To: SCHOTTENFELD OPPORTUNITIES FUND II, L.P.
Reel/Frame 051072/0310 →
SECURITY INTEREST Recorded Aug 16, 2019
From: AMYRIS, INC.
To: NAXYRIS S.A.
Reel/Frame 050081/0106 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 3, 2017
From: UEHARA, YOSUKE; SASAKI, HIROMITSU; KONISHI, DAISUKE; KATO, MASAHIRO
To: KURARAY CO., LTD.; AMYRIS, INC.
Reel/Frame 043189/0734 →