RU96110885A - MULTI-BLOCK HYDROGENIZED POLYMERS FOR ADHESIVES - Google Patents
MULTI-BLOCK HYDROGENIZED POLYMERS FOR ADHESIVESInfo
- Publication number
- RU96110885A RU96110885A RU96110885/04A RU96110885A RU96110885A RU 96110885 A RU96110885 A RU 96110885A RU 96110885/04 A RU96110885/04 A RU 96110885/04A RU 96110885 A RU96110885 A RU 96110885A RU 96110885 A RU96110885 A RU 96110885A
- Authority
- RU
- Russia
- Prior art keywords
- molecular weight
- denotes
- copolymer
- range
- polymer block
- Prior art date
Links
- 229920000642 polymer Polymers 0.000 title claims 10
- 239000000853 adhesive Substances 0.000 title claims 2
- 229920001577 copolymer Polymers 0.000 claims 9
- 238000005984 hydrogenation reaction Methods 0.000 claims 7
- 150000001993 dienes Chemical class 0.000 claims 6
- 229920001400 block copolymer Polymers 0.000 claims 5
- KAKZBPTYRLMSJV-UHFFFAOYSA-N butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims 5
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 5
- RRHGJUQNOFWUDK-UHFFFAOYSA-N isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims 4
- 238000010606 normalization Methods 0.000 claims 4
- -1 vinyl aromatic hydrocarbon Chemical class 0.000 claims 3
- 239000003795 chemical substances by application Substances 0.000 claims 2
- 230000001070 adhesive Effects 0.000 claims 1
- 239000011347 resin Substances 0.000 claims 1
- 229920005989 resin Polymers 0.000 claims 1
Claims (14)
D-A-(B-A)n-Dx и/или (D-A-B)q-Y,
где A обозначает винилароматический углеводородный полимерный блок, молекулярная масса которого составляет от 4000 до 35000;
B обозначает гидрогенизованный сопряженный диеновый полимерный блок, молекулярная масса которого равна от 20000 до 200000;
D обозначает гидрогенизованный сопряженный диеновый полимерный блок, молекулярная масса которого составляет от 5000 до 50000, причем, когда либо B, либо D является бутадиеном до гидрогенизации, содержание виниловых звеньев равно от 30 до 65 вес.%, соотношение между молекулярной массой D и молекулярной массой B варьируется так, что показатель нормализованной молекулярной массы находится в пределах от более 0 до 180•10-6;
n обозначает целое число от 1 до 5;
x обозначает 0 или 1;
q равно от 2 до 30;
Y обозначает мультиблочный агент сочетания,
а содержание винилароматических углеводородных звеньев в сополимере составляет от 9 до 35 вес.%, и (б) повышающую липкость смолу.1. The adhesive composition comprising (a) a multi-block copolymer of the formula
DA- (BA) n -D x and / or (DAB) q -Y,
where A denotes a vinyl aromatic hydrocarbon polymer block, the molecular weight of which ranges from 4,000 to 35,000;
B denotes a hydrogenated conjugated diene polymer block whose molecular weight is from 20,000 to 200,000;
D denotes a hydrogenated conjugated diene polymer block whose molecular weight is from 5,000 to 50,000, and when either B or D is butadiene before hydrogenation, the content of vinyl units is from 30 to 65 wt.%, The ratio between molecular weight D and molecular weight B varies so that the rate of normalized molecular weight ranges from more than 0 to 180 • 10 -6 ;
n represents an integer from 1 to 5;
x is 0 or 1;
q is from 2 to 30;
Y stands for multiblock combination agent,
and the content of vinyl aromatic hydrocarbon units in the copolymer is from 9 to 35% by weight, and (b) the tackifying resin.
(D-A-B)q-Y,
где A обозначает винилароматический углеводородный полимерный блок, молекулярная масса которого составляет от 4000 до 35000;
B обозначает гидрогенизованный сопряженный диеновый полимерный блок, молекулярная масса которого равна от 20000 до 200000;
D обозначает гидрогенизованный сопряженный диеновый полимерный блок, молекулярная масса которого равна от 5000 до 50000, причем, когда B или D обозначает бутадиен до гидрогенизации, содержание виниловых звеньев составляет от 30 до 65 вес.%, а соотношение между молекулярной массой D и молекулярной массой B находится в таком интервале, что показатель нормализованной молекулярной массы находится в интервале от более 0 до 180•10-6;
q равно от 2 до 30;
Y обозначает мультиблочный агент сочетания,
а содержание винилароматических углеводородных звеньев в сополимере составляет от 9 до 35 вес.%.7. Not twisted into a spiral multi-block copolymer of the formula
(DAB) q -Y,
where A denotes a vinyl aromatic hydrocarbon polymer block, the molecular weight of which ranges from 4,000 to 35,000;
B denotes a hydrogenated conjugated diene polymer block whose molecular weight is from 20,000 to 200,000;
D denotes a hydrogenated conjugated diene polymer block whose molecular weight is from 5,000 to 50,000, and when B or D stands for butadiene before hydrogenation, the content of vinyl units ranges from 30 to 65% by weight, and the ratio between molecular weight D and molecular weight B is in the range that the normalized molecular weight index is in the range from more than 0 to 180 • 10 -6 ;
q is from 2 to 30;
Y stands for multiblock combination agent,
and the content of vinyl aromatic hydrocarbon units in the copolymer is from 9 to 35 wt.%.
D-A-(B-A)n-D,
где A обозначает винилароматический углеводородный полимерный блок, молекулярная масса которого составляет от 4000 до 35000;
B обозначает гидрогенизованный сопряженный диеновый полимерный блок, молекулярная масса которого равна от 20000 до 200000;
D обозначает гидрогенизованный сопряженный диеновый полимерный блок, молекулярная масса которого равна от 5000 до 50000, причем, когда B и D обозначает бутадиен до гидрогенизации, содержание виниловых звеньев составляет от 30 до 65 вес.%, соотношение между молекулярной массой D и молекулярной массой B находится в таком интервале, что показатель нормализованной молекулярной массы находится в интервале от более 0 до 180•10-6;
n обозначает целое число от 1 до 5,
а содержание винилароматических углеводородных звеньев в сополимере составляет от 9 до 35 вес.%.10. Not twisted into a spiral multi-block copolymer of the formula
DA- (BA) n -D,
where A denotes a vinyl aromatic hydrocarbon polymer block, the molecular weight of which ranges from 4,000 to 35,000;
B denotes a hydrogenated conjugated diene polymer block whose molecular weight is from 20,000 to 200,000;
D denotes a hydrogenated conjugated diene polymer block whose molecular weight is from 5,000 to 50,000, and when B and D denotes butadiene before hydrogenation, the content of vinyl units is from 30 to 65 wt.%, The ratio between molecular weight D and molecular weight B is in the range that the normalized molecular weight index is in the range from more than 0 to 180 • 10 -6 ;
n denotes an integer from 1 to 5,
and the content of vinyl aromatic hydrocarbon units in the copolymer is from 9 to 35 wt.%.
Applications Claiming Priority (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US14721893A | 1993-11-03 | 1993-11-03 | |
US08/147218 | 1993-11-03 | ||
US08/320,033 US5589542A (en) | 1993-11-03 | 1994-10-07 | Multiblock hydrogenated polymers for adhesives |
US08/320033 | 1994-10-07 | ||
US08/320,033 | 1994-10-07 | ||
US08/147,218 | 1994-10-07 |
Publications (2)
Publication Number | Publication Date |
---|---|
RU96110885A true RU96110885A (en) | 1998-09-27 |
RU2160755C2 RU2160755C2 (en) | 2000-12-20 |
Family
ID=26844698
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU96110885/04A RU2160755C2 (en) | 1993-11-03 | 1994-10-31 | Multiblock hydrogenated polymers for adhesives |
Country Status (15)
Country | Link |
---|---|
US (3) | US5589542A (en) |
EP (1) | EP0726927B1 (en) |
JP (1) | JP3556224B2 (en) |
KR (1) | KR100346241B1 (en) |
CN (1) | CN1066182C (en) |
AT (1) | ATE163031T1 (en) |
AU (1) | AU687131B2 (en) |
BR (1) | BR9407936A (en) |
CA (1) | CA2175580A1 (en) |
DE (1) | DE69408474T2 (en) |
DK (1) | DK0726927T3 (en) |
ES (1) | ES2111966T3 (en) |
NO (1) | NO308906B1 (en) |
RU (1) | RU2160755C2 (en) |
WO (1) | WO1995012645A1 (en) |
Families Citing this family (35)
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US5777043A (en) * | 1997-03-05 | 1998-07-07 | Shell Oil Company | Sealant formulations containing high vinyl content hydrogenated styrene-butadiene-styrene block copolymers |
DE19815895C2 (en) * | 1997-04-09 | 2000-04-13 | Asahi Chemical Ind | Hydrogenated block copolymers, compositions containing them and moldings |
DE69914109T2 (en) * | 1998-08-27 | 2004-11-18 | Kraton Polymers Research B.V. | MELT ADHESIVE COMPOSITION WITH HIGH RESEARCH RESISTANCE AND HIGH CAPACITY |
US6221483B1 (en) | 1998-09-10 | 2001-04-24 | Avery Dennison Corporation | Reversibly extensible film |
US6455627B1 (en) * | 1999-06-25 | 2002-09-24 | Kraton Polymers Us Llc | Hot melt pressure sensitive positions adhesive (II) |
US6451913B1 (en) * | 1999-09-01 | 2002-09-17 | Kraton Polymers U.S. Llc | Radial hydrogenated block copolymers showing one phase melt behavior |
EP1299475A1 (en) * | 2000-06-27 | 2003-04-09 | ExxonMobil Chemical Patents Inc. | Tetrablock copolymers |
EP1905808B1 (en) | 2000-06-27 | 2011-05-25 | ExxonMobil Chemical Patents Inc. | Adhesives with improved die-cutting performance |
JP5442176B2 (en) * | 2000-06-27 | 2014-03-12 | トリムルティ ホールディング コーポレイション | Adhesive with improved punching performance |
US6576686B1 (en) | 2000-06-27 | 2003-06-10 | Exxonmobil Chemical Patents Inc. | Road marking compound comprising linear tetrablock copolymers |
JP3938270B2 (en) * | 2000-06-29 | 2007-06-27 | 三菱電機株式会社 | Optical repeater amplifier |
US6362282B1 (en) * | 2000-09-29 | 2002-03-26 | Firestone Polymers, Llc | Polymers with high vinyl end segments |
US7268184B2 (en) * | 2002-01-31 | 2007-09-11 | Kraton Polymers U.S. Llc | Blockcopolymer compositions, having improved mechanical properties and processability and styrenic blockcopolymer to be used in them |
EP1333058A1 (en) * | 2002-01-31 | 2003-08-06 | KRATON Polymers Research B.V. | Modified styrenic block copolymer and compounds thereof having improved mechanical properties and processability |
AU2003202559A1 (en) * | 2002-01-31 | 2003-09-02 | Kraton Polymers Research B.V. | Block copolymer compositions, having improved mechanical properties and processability |
CN101696248B (en) | 2002-04-10 | 2012-07-25 | 旭化成化学株式会社 | Modified polymers and compositions containing the same |
KR20040032488A (en) * | 2002-10-10 | 2004-04-17 | 금호석유화학 주식회사 | Ternary block copolymer and menufacturing method of the same |
DE602004014593D1 (en) * | 2003-02-21 | 2008-08-07 | Kraton Polymers Res Bv | LABEL PREMATURE WITH IMPROVED PUNCHING BEHAVIOR |
KR100718353B1 (en) * | 2003-02-21 | 2007-05-14 | 크레이튼 폴리머즈 리서치 비.브이. | Adhesive composition and tapes and labels derived therefrom |
EP1449898A1 (en) * | 2003-02-21 | 2004-08-25 | KRATON Polymers Research B.V. | Adhesive composition and tapes and labels derived therefrom |
US7517932B2 (en) * | 2003-03-24 | 2009-04-14 | Kraton Polymers U.S. Llc | Poly(styrene-butadiene-styrene)polymers having a high vinyl content in the butadiene block and hot melt adhesive composition comprising said polymers |
US6916750B2 (en) * | 2003-03-24 | 2005-07-12 | Kimberly-Clark Worldwide, Inc. | High performance elastic laminates made from high molecular weight styrenic tetrablock copolymer |
EP1553149A1 (en) * | 2003-12-31 | 2005-07-13 | Kraton Polymers Research B.V. | Low viscosity, hot-melt stable adhesive compositions |
WO2005075594A1 (en) * | 2004-02-06 | 2005-08-18 | Kraton Polymers Research B.V. | Pressure sensitive adhesive and compositions prepared with same |
KR100830024B1 (en) | 2004-03-03 | 2008-05-15 | 크레이튼 폴리머즈 리서치 비.브이. | Block copolymers having high flow and high elasticity |
DE602005009514D1 (en) * | 2004-03-25 | 2008-10-16 | Kraton Polymers Res Bv | THERMOPLASTIC GEL COMPOSITIONS THAT CAN BE CONVERTED BY IRRADIATION IN DUROPLASTIC GEL COMPOSITIONS |
US7262248B2 (en) * | 2004-05-11 | 2007-08-28 | Kraton Polymers U.S. Llc | Articles prepared from high molecular weight tetrablock copolymers |
US7651653B2 (en) | 2004-12-22 | 2010-01-26 | Kimberly-Clark Worldwide, Inc. | Machine and cross-machine direction elastic materials and methods of making same |
US7645507B2 (en) * | 2005-10-24 | 2010-01-12 | Kraton Polymers U.S. Llc | Protective films and pressure sensitive adhesives |
JP4571689B2 (en) * | 2006-04-28 | 2010-10-27 | Jsr株式会社 | Adhesive composition, method for producing the same, and adhesive |
WO2010024382A1 (en) | 2008-08-29 | 2010-03-04 | 株式会社クラレ | Hydrogenated block copolymer and composition containing same |
JP6272468B2 (en) * | 2014-05-19 | 2018-01-31 | 旭化成株式会社 | Hydrogenated block copolymer composition and adhesive composition |
JP7176522B2 (en) * | 2017-08-30 | 2022-11-22 | 日本ゼオン株式会社 | Binder composition for non-aqueous secondary battery electrode, slurry composition for non-aqueous secondary battery electrode, electrode for non-aqueous secondary battery, and non-aqueous secondary battery |
US11466115B2 (en) * | 2018-06-01 | 2022-10-11 | 3M Innovative Properties Company | Porous membranes including triblock copolymers |
JP7502347B2 (en) * | 2019-06-21 | 2024-06-18 | ピュアウィック コーポレイション | Fluid collection devices including base fastening regions and related systems and methods - Patents.com |
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JPS5938029A (en) * | 1982-08-25 | 1984-03-01 | Denki Kagaku Kogyo Kk | Transparent heat-shrinkable film |
JPH0621136B2 (en) * | 1984-04-26 | 1994-03-23 | シエル・インターナシヨナル・リサーチ・マートスハツペイ・ベー・ヴエー | Block copolymer |
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IT1222429B (en) * | 1987-07-31 | 1990-09-05 | Enichem Elastromeri S P A | BLOCK COPOLYMER PROCEDURE FOR ITS PREPARATION |
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IT1227927B (en) * | 1988-11-25 | 1991-05-14 | Enichem Elastomers | LINEAR COPOLYMERS WITH ALTERNATE BLOCKS. |
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US5292820A (en) * | 1990-01-16 | 1994-03-08 | Mobil Oil Corporation | Solid elastomeric block copolymers |
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US5120765A (en) * | 1990-09-28 | 1992-06-09 | Shell Oil Company | Block copolymer dispersions and process to prepare block copolymer dispersions |
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-
1994
- 1994-10-07 US US08/320,033 patent/US5589542A/en not_active Ceased
- 1994-10-31 ES ES94931557T patent/ES2111966T3/en not_active Expired - Lifetime
- 1994-10-31 JP JP51302095A patent/JP3556224B2/en not_active Expired - Lifetime
- 1994-10-31 DK DK94931557.6T patent/DK0726927T3/en active
- 1994-10-31 RU RU96110885/04A patent/RU2160755C2/en not_active IP Right Cessation
- 1994-10-31 DE DE69408474T patent/DE69408474T2/en not_active Expired - Fee Related
- 1994-10-31 EP EP94931557A patent/EP0726927B1/en not_active Expired - Lifetime
- 1994-10-31 KR KR1019960702287A patent/KR100346241B1/en not_active IP Right Cessation
- 1994-10-31 WO PCT/EP1994/003608 patent/WO1995012645A1/en active IP Right Grant
- 1994-10-31 AU AU11073/95A patent/AU687131B2/en not_active Ceased
- 1994-10-31 BR BR9407936A patent/BR9407936A/en not_active IP Right Cessation
- 1994-10-31 AT AT94931557T patent/ATE163031T1/en not_active IP Right Cessation
- 1994-10-31 CN CN94194396A patent/CN1066182C/en not_active Expired - Fee Related
- 1994-10-31 CA CA002175580A patent/CA2175580A1/en not_active Abandoned
-
1995
- 1995-10-26 US US08/548,719 patent/US5627235A/en not_active Expired - Lifetime
-
1996
- 1996-04-30 NO NO961760A patent/NO308906B1/en not_active IP Right Cessation
-
1997
- 1997-02-26 US US08/805,599 patent/USRE36757E/en not_active Expired - Lifetime
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