KR20110030438A - (메트)아크릴레이트에 기초한 실릴-관능화된 ａｂａ 트리블록 공중합체의 제조 방법 - Google Patents
(메트)아크릴레이트에 기초한 실릴-관능화된 ａｂａ 트리블록 공중합체의 제조 방법 Download PDFInfo
- Publication number
- KR20110030438A KR20110030438A KR1020107026535A KR20107026535A KR20110030438A KR 20110030438 A KR20110030438 A KR 20110030438A KR 1020107026535 A KR1020107026535 A KR 1020107026535A KR 20107026535 A KR20107026535 A KR 20107026535A KR 20110030438 A KR20110030438 A KR 20110030438A
- Authority
- KR
- South Korea
- Prior art keywords
- block
- silyl
- meth
- block copolymer
- acrylates
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
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- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 title claims description 23
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 229920000428 triblock copolymer Polymers 0.000 title abstract description 12
- 238000000034 method Methods 0.000 claims abstract description 38
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims abstract description 33
- 230000008569 process Effects 0.000 claims abstract description 21
- 239000000203 mixture Substances 0.000 claims description 67
- 239000000178 monomer Substances 0.000 claims description 52
- 229920000642 polymer Polymers 0.000 claims description 48
- 229920001400 block copolymer Polymers 0.000 claims description 41
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 claims description 32
- 238000006116 polymerization reaction Methods 0.000 claims description 26
- 238000010560 atom transfer radical polymerization reaction Methods 0.000 claims description 21
- 238000009826 distribution Methods 0.000 claims description 16
- 229920001577 copolymer Polymers 0.000 claims description 14
- 239000003999 initiator Substances 0.000 claims description 14
- 239000000565 sealant Substances 0.000 claims description 14
- 238000007306 functionalization reaction Methods 0.000 claims description 13
- 239000003446 ligand Substances 0.000 claims description 13
- 239000003054 catalyst Substances 0.000 claims description 11
- 150000001875 compounds Chemical class 0.000 claims description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- 239000002904 solvent Substances 0.000 claims description 7
- 150000003623 transition metal compounds Chemical class 0.000 claims description 6
- 230000001588 bifunctional effect Effects 0.000 claims description 5
- 238000001914 filtration Methods 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 125000004122 cyclic group Chemical group 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 239000004831 Hot glue Substances 0.000 claims description 2
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 claims description 2
- 238000004026 adhesive bonding Methods 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 239000013522 chelant Substances 0.000 claims description 2
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- 239000005749 Copper compound Substances 0.000 claims 1
- 150000001880 copper compounds Chemical class 0.000 claims 1
- 238000002360 preparation method Methods 0.000 abstract description 3
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 description 19
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- 239000000243 solution Substances 0.000 description 15
- -1 cyclic dienes Chemical class 0.000 description 14
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- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 10
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- 238000003786 synthesis reaction Methods 0.000 description 7
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 7
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
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- LHZBJSPSWKIJKZ-UHFFFAOYSA-N 4-(2-bromo-2-methylpropanoyl)oxybutyl 2-bromo-2-methylpropanoate Chemical compound CC(C)(Br)C(=O)OCCCCOC(=O)C(C)(C)Br LHZBJSPSWKIJKZ-UHFFFAOYSA-N 0.000 description 4
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 4
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- 230000008901 benefit Effects 0.000 description 4
- 239000010949 copper Substances 0.000 description 4
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 238000010526 radical polymerization reaction Methods 0.000 description 4
- 238000012546 transfer Methods 0.000 description 4
- XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 description 3
- 239000005751 Copper oxide Substances 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- 238000005481 NMR spectroscopy Methods 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 238000010276 construction Methods 0.000 description 3
- 229910000431 copper oxide Inorganic materials 0.000 description 3
- 238000011161 development Methods 0.000 description 3
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
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- 230000002028 premature Effects 0.000 description 3
- 238000007342 radical addition reaction Methods 0.000 description 3
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- 230000002441 reversible effect Effects 0.000 description 3
- 239000000741 silica gel Substances 0.000 description 3
- 229910002027 silica gel Inorganic materials 0.000 description 3
- 150000003440 styrenes Chemical group 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- ZGEGCLOFRBLKSE-UHFFFAOYSA-N 1-Heptene Chemical compound CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 2
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
- PGMMQIGGQSIEGH-UHFFFAOYSA-N 2-ethenyl-1,3-oxazole Chemical compound C=CC1=NC=CO1 PGMMQIGGQSIEGH-UHFFFAOYSA-N 0.000 description 2
- JDCUKFVNOWJNBU-UHFFFAOYSA-N 2-ethenyl-1,3-thiazole Chemical compound C=CC1=NC=CS1 JDCUKFVNOWJNBU-UHFFFAOYSA-N 0.000 description 2
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 2
- 229910021589 Copper(I) bromide Inorganic materials 0.000 description 2
- 229910021591 Copper(I) chloride Inorganic materials 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 2
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- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
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- AYOHIQLKSOJJQH-UHFFFAOYSA-N dibutyltin Chemical compound CCCC[Sn]CCCC AYOHIQLKSOJJQH-UHFFFAOYSA-N 0.000 description 2
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- 125000005843 halogen group Chemical group 0.000 description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-M hexanoate Chemical compound CCCCCC([O-])=O FUZZWVXGSFPDMH-UHFFFAOYSA-M 0.000 description 2
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- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
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Classifications
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/10—Materials in mouldable or extrudable form for sealing or packing joints or covers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F293/00—Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule
- C08F293/005—Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule using free radical "living" or "controlled" polymerisation, e.g. using a complexing agent
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L53/00—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L53/005—Modified block copolymers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J153/00—Adhesives based on block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers
- C09J153/005—Modified block copolymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2200/00—Chemical nature of materials in mouldable or extrudable form for sealing or packing joints or covers
- C09K2200/06—Macromolecular organic compounds, e.g. prepolymers
- C09K2200/0615—Macromolecular organic compounds, e.g. prepolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C09K2200/0625—Polyacrylic esters or derivatives thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Graft Or Block Polymers (AREA)
- Sealing Material Composition (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102008002016A DE102008002016A1 (de) | 2008-05-28 | 2008-05-28 | Verfahren zur Herstellung von silyl-funktionalisierten ABA-Triblockcopolymeren auf (Meth)acrylatbasis |
| DE102008002016.8 | 2008-05-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20110030438A true KR20110030438A (ko) | 2011-03-23 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020107026535A Withdrawn KR20110030438A (ko) | 2008-05-28 | 2009-04-14 | (메트)아크릴레이트에 기초한 실릴-관능화된 ａｂａ 트리블록 공중합체의 제조 방법 |
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| Country | Link |
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| US (1) | US8431652B2 (enExample) |
| EP (1) | EP2285849B1 (enExample) |
| JP (1) | JP5661611B2 (enExample) |
| KR (1) | KR20110030438A (enExample) |
| CN (2) | CN102046678A (enExample) |
| AU (1) | AU2009253311A1 (enExample) |
| CA (1) | CA2725584A1 (enExample) |
| DE (1) | DE102008002016A1 (enExample) |
| WO (1) | WO2009144082A1 (enExample) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20100137520A (ko) | 2008-03-20 | 2010-12-30 | 애버리 데니슨 코포레이션 | 작용기의 위치가 조절된 아크릴 중합체 |
| DE102008025575A1 (de) | 2008-05-28 | 2009-12-03 | Evonik Röhm Gmbh | Mit Wasser vernetzbare Dichtmasse |
| DE102008043674A1 (de) | 2008-11-12 | 2010-05-20 | Evonik Röhm Gmbh | Verfahren zur Herstellung von Telechelen mit einer bimodalen Molekulkargewichtsverteilung |
| DE102008043668A1 (de) | 2008-11-12 | 2010-05-20 | Evonik Röhm Gmbh | Verfahren zur Herstellung von ABA-Triblockcopolymeren mit einem bimodalen B-Block |
| DE102008043658A1 (de) | 2008-11-12 | 2010-05-20 | Evonik Röhm Gmbh | Verfahren zur Herstellung von AB-Diblockcopolymeren mit einem breit verteilten A-Block |
| DE102008043662A1 (de) | 2008-11-12 | 2010-05-20 | Evonik Röhm Gmbh | Verfahren zur Herstellung von Telechelen mit breiter Molekulargewichtsverteilung |
| DE102008043666A1 (de) | 2008-11-12 | 2010-05-20 | Evonik Röhm Gmbh | Verfahren zur Herstellung von AB-Diblockcopolymeren mit einem bimodalen verteilten A-Block |
| DE102008043669A1 (de) | 2008-11-12 | 2010-05-20 | Evonik Röhm Gmbh | Verfahren zur Herstellung von ABA-Triblockcopolymeren mit einem breit verteilten B-Block |
| DE102009001771A1 (de) | 2009-03-24 | 2010-09-30 | Henkel Ag & Co. Kgaa | Erstarrende Klebstoffe mit Silanvernetzung |
| DE102009027620A1 (de) | 2009-07-10 | 2011-01-13 | Evonik Röhm Gmbh | Copolymerisation von Silyl-funktionellen Komponenten in wässrigen Polymerisationssystemen |
| DE102009046190A1 (de) | 2009-10-30 | 2011-05-05 | Henkel Ag & Co. Kgaa | Kaschierklebstoff mit Silanvernetzung |
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-
2008
- 2008-05-28 DE DE102008002016A patent/DE102008002016A1/de not_active Withdrawn
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2009
- 2009-04-14 AU AU2009253311A patent/AU2009253311A1/en not_active Abandoned
- 2009-04-14 KR KR1020107026535A patent/KR20110030438A/ko not_active Withdrawn
- 2009-04-14 US US12/992,430 patent/US8431652B2/en not_active Expired - Fee Related
- 2009-04-14 EP EP09753737.7A patent/EP2285849B1/de not_active Not-in-force
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- 2009-04-14 CA CA2725584A patent/CA2725584A1/en not_active Abandoned
- 2009-04-14 WO PCT/EP2009/054364 patent/WO2009144082A1/de not_active Ceased
- 2009-04-14 CN CN201510092308.8A patent/CN104710585A/zh active Pending
- 2009-04-14 JP JP2011510918A patent/JP5661611B2/ja not_active Expired - Fee Related
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| US8431652B2 (en) | 2013-04-30 |
| JP5661611B2 (ja) | 2015-01-28 |
| CA2725584A1 (en) | 2009-12-03 |
| JP2011522074A (ja) | 2011-07-28 |
| EP2285849A1 (de) | 2011-02-23 |
| CN102046678A (zh) | 2011-05-04 |
| EP2285849B1 (de) | 2014-06-18 |
| WO2009144082A1 (de) | 2009-12-03 |
| DE102008002016A1 (de) | 2009-12-03 |
| AU2009253311A1 (en) | 2009-12-03 |
| CN104710585A (zh) | 2015-06-17 |
| US20110086984A1 (en) | 2011-04-14 |
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