DE102008000914A1 - Verfahren zur Synthese von verbesserten Bindemitteln und veränderter Taktizität - Google Patents
Verfahren zur Synthese von verbesserten Bindemitteln und veränderter Taktizität Download PDFInfo
- Publication number
- DE102008000914A1 DE102008000914A1 DE102008000914A DE102008000914A DE102008000914A1 DE 102008000914 A1 DE102008000914 A1 DE 102008000914A1 DE 102008000914 A DE102008000914 A DE 102008000914A DE 102008000914 A DE102008000914 A DE 102008000914A DE 102008000914 A1 DE102008000914 A1 DE 102008000914A1
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- Prior art keywords
- meth
- polymerization
- acrylate
- binder
- preparation
- Prior art date
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- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- XRXPHPJRVWEWKQ-UHFFFAOYSA-N cyclohexyloxymethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCOC1CCCCC1 XRXPHPJRVWEWKQ-UHFFFAOYSA-N 0.000 description 1
- XJOBOFWTZOKMOH-UHFFFAOYSA-N decanoyl decaneperoxoate Chemical compound CCCCCCCCCC(=O)OOC(=O)CCCCCCCCC XJOBOFWTZOKMOH-UHFFFAOYSA-N 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 238000004455 differential thermal analysis Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 150000002084 enol ethers Chemical class 0.000 description 1
- LDLDYFCCDKENPD-UHFFFAOYSA-N ethenylcyclohexane Chemical compound C=CC1CCCCC1 LDLDYFCCDKENPD-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- WMAFNLQQGPUKCM-UHFFFAOYSA-N ethoxymethyl 2-methylprop-2-enoate Chemical compound CCOCOC(=O)C(C)=C WMAFNLQQGPUKCM-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- DNJIEGIFACGWOD-UHFFFAOYSA-N ethyl mercaptane Natural products CCS DNJIEGIFACGWOD-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- DWXAVNJYFLGAEF-UHFFFAOYSA-N furan-2-ylmethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC1=CC=CO1 DWXAVNJYFLGAEF-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 229920001580 isotactic polymer Polymers 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 229920001427 mPEG Polymers 0.000 description 1
- 150000002688 maleic acid derivatives Chemical class 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 239000012452 mother liquor Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- QUWPKSVNVOPLKX-UHFFFAOYSA-N octan-3-yl 2-sulfanylacetate Chemical compound CCCCCC(CC)OC(=O)CS QUWPKSVNVOPLKX-UHFFFAOYSA-N 0.000 description 1
- KZCOBXFFBQJQHH-UHFFFAOYSA-N octane-1-thiol Chemical compound CCCCCCCCS KZCOBXFFBQJQHH-UHFFFAOYSA-N 0.000 description 1
- SRSFOMHQIATOFV-UHFFFAOYSA-N octanoyl octaneperoxoate Chemical compound CCCCCCCC(=O)OOC(=O)CCCCCCC SRSFOMHQIATOFV-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 150000002976 peresters Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- XGRBZUSXGVNWMI-UHFFFAOYSA-N phenylmethoxymethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCOCC1=CC=CC=C1 XGRBZUSXGVNWMI-UHFFFAOYSA-N 0.000 description 1
- 125000005498 phthalate group Chemical class 0.000 description 1
- 230000019612 pigmentation Effects 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- CHKVPAROMQMJNQ-UHFFFAOYSA-M potassium bisulfate Chemical compound [K+].OS([O-])(=O)=O CHKVPAROMQMJNQ-UHFFFAOYSA-M 0.000 description 1
- 229910000343 potassium bisulfate Inorganic materials 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000013074 reference sample Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003203 stereoselective catalyst Substances 0.000 description 1
- 230000000707 stereoselective effect Effects 0.000 description 1
- 230000003335 steric effect Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 description 1
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- BWSZXUOMATYHHI-UHFFFAOYSA-N tert-butyl octaneperoxoate Chemical compound CCCCCCCC(=O)OOC(C)(C)C BWSZXUOMATYHHI-UHFFFAOYSA-N 0.000 description 1
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 1
- 238000006276 transfer reaction Methods 0.000 description 1
- 230000007306 turnover Effects 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
- DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D133/04—Homopolymers or copolymers of esters
-
- 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
- C08F2/00—Processes of polymerisation
- C08F2/02—Polymerisation in bulk
-
- 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
- C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F20/02—Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
- C08F20/10—Esters
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Materials Engineering (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Paints Or Removers (AREA)
- Sealing Material Composition (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Graft Or Block Polymers (AREA)
Priority Applications (11)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102008000914A DE102008000914A1 (de) | 2008-04-01 | 2008-04-01 | Verfahren zur Synthese von verbesserten Bindemitteln und veränderter Taktizität |
| EP09728210A EP2276817A1 (de) | 2008-04-01 | 2009-02-02 | Verfahren zur synthese von verbesserten bindemitteln und veränderter taktizität |
| US12/864,363 US8426497B2 (en) | 2008-04-01 | 2009-02-02 | Synthesis of improved binders and modified tacticity |
| PCT/EP2009/051117 WO2009121640A1 (de) | 2008-04-01 | 2009-02-02 | Verfahren zur synthese von verbesserten bindemitteln und veränderter taktizität |
| RU2010144330/05A RU2010144330A (ru) | 2008-04-01 | 2009-02-02 | Способ синтеза улучшенных связующих с модифицированной регулярностью микроструктуры |
| JP2011502306A JP5634982B2 (ja) | 2008-04-01 | 2009-02-02 | 改良された結合剤及び変性タクチシティの合成法 |
| CA2719850A CA2719850A1 (en) | 2008-04-01 | 2009-02-02 | Synthesis of improved binders and modified tacticity |
| BRPI0910448A BRPI0910448A2 (pt) | 2008-04-01 | 2009-02-02 | síntese dos aglutinantes melhorados e taticidade modificada |
| TW098110167A TWI498390B (zh) | 2008-04-01 | 2009-03-27 | 具有修飾的立體規整度之改良的黏合劑之合成方法 |
| CN200910132534.9A CN101550310B (zh) | 2008-04-01 | 2009-03-31 | 合成改善的粘结剂和改变的立构规整度的方法 |
| HK10103402.4A HK1138309B (en) | 2008-04-01 | 2010-04-07 | Process for synthesis of improved binder modified tacticity |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102008000914A DE102008000914A1 (de) | 2008-04-01 | 2008-04-01 | Verfahren zur Synthese von verbesserten Bindemitteln und veränderter Taktizität |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE102008000914A1 true DE102008000914A1 (de) | 2009-10-08 |
Family
ID=40591976
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE102008000914A Withdrawn DE102008000914A1 (de) | 2008-04-01 | 2008-04-01 | Verfahren zur Synthese von verbesserten Bindemitteln und veränderter Taktizität |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US8426497B2 (https=) |
| EP (1) | EP2276817A1 (https=) |
| JP (1) | JP5634982B2 (https=) |
| CN (1) | CN101550310B (https=) |
| BR (1) | BRPI0910448A2 (https=) |
| CA (1) | CA2719850A1 (https=) |
| DE (1) | DE102008000914A1 (https=) |
| RU (1) | RU2010144330A (https=) |
| TW (1) | TWI498390B (https=) |
| WO (1) | WO2009121640A1 (https=) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102009000814A1 (de) * | 2009-02-12 | 2010-08-19 | Evonik Röhm Gmbh | Verfahren zur Synthese von verbesserten Bindemitteln mit definierter Korngrößenverteilung |
| DE102009046922A1 (de) * | 2009-11-20 | 2011-05-26 | Evonik Röhm Gmbh | Substanzpolymerisation von (Meth)acrylat-Copolymeren, die im Wässrig-alkalischen löslich sind |
| WO2018161025A1 (en) * | 2017-03-02 | 2018-09-07 | Nitto Denko Corporation | Ionic compositions and related uses thereof |
| CN109535838B (zh) * | 2018-11-27 | 2021-11-23 | 山东国瓷康立泰新材料科技有限公司 | 一种光泽度可调的精雕效果的陶瓷喷墨打印墨水及其制备方法 |
| KR102852425B1 (ko) * | 2021-10-28 | 2025-08-29 | 주식회사 엘엑스엠엠에이 | 자외선 투과율이 우수한 uv살균용 아크릴계 공중합체의 제조방법 |
| CN116650695B (zh) * | 2023-07-28 | 2023-10-13 | 山东亘泽医疗科技有限公司 | 压力蒸汽灭菌化学指示物的制备工艺 |
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| WO1998004593A1 (en) | 1996-07-26 | 1998-02-05 | Henkel Corporation | Solid acrylic resin using a continuous tube reactor |
| WO1998012229A1 (de) | 1996-09-18 | 1998-03-26 | Basf Aktiengesellschaft | Verfahren zur herstellung von methylmethacrylat-polymeren in einem kreislaufreaktor |
| WO1999023119A1 (en) | 1997-10-31 | 1999-05-14 | Cognis Corporation | Continuous bulk polymerization process |
| US6476170B1 (en) | 1996-07-26 | 2002-11-05 | Cook Composites & Polymers Co. | Solid acrylic resin using a continuous tube reactor |
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-
2008
- 2008-04-01 DE DE102008000914A patent/DE102008000914A1/de not_active Withdrawn
-
2009
- 2009-02-02 CA CA2719850A patent/CA2719850A1/en not_active Abandoned
- 2009-02-02 EP EP09728210A patent/EP2276817A1/de not_active Ceased
- 2009-02-02 JP JP2011502306A patent/JP5634982B2/ja active Active
- 2009-02-02 US US12/864,363 patent/US8426497B2/en not_active Expired - Fee Related
- 2009-02-02 BR BRPI0910448A patent/BRPI0910448A2/pt not_active IP Right Cessation
- 2009-02-02 RU RU2010144330/05A patent/RU2010144330A/ru unknown
- 2009-02-02 WO PCT/EP2009/051117 patent/WO2009121640A1/de not_active Ceased
- 2009-03-27 TW TW098110167A patent/TWI498390B/zh active
- 2009-03-31 CN CN200910132534.9A patent/CN101550310B/zh active Active
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Also Published As
| Publication number | Publication date |
|---|---|
| RU2010144330A (ru) | 2012-05-10 |
| TWI498390B (zh) | 2015-09-01 |
| EP2276817A1 (de) | 2011-01-26 |
| HK1138309A1 (en) | 2010-08-20 |
| CN101550310B (zh) | 2014-10-22 |
| WO2009121640A1 (de) | 2009-10-08 |
| CN101550310A (zh) | 2009-10-07 |
| JP2011518238A (ja) | 2011-06-23 |
| CA2719850A1 (en) | 2009-10-08 |
| BRPI0910448A2 (pt) | 2015-09-29 |
| TW201006897A (en) | 2010-02-16 |
| JP5634982B2 (ja) | 2014-12-03 |
| US20100298466A1 (en) | 2010-11-25 |
| US8426497B2 (en) | 2013-04-23 |
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