CA2719850A1 - Synthesis of improved binders and modified tacticity - Google Patents
Synthesis of improved binders and modified tacticity Download PDFInfo
- Publication number
- CA2719850A1 CA2719850A1 CA2719850A CA2719850A CA2719850A1 CA 2719850 A1 CA2719850 A1 CA 2719850A1 CA 2719850 A CA2719850 A CA 2719850A CA 2719850 A CA2719850 A CA 2719850A CA 2719850 A1 CA2719850 A1 CA 2719850A1
- Authority
- CA
- Canada
- Prior art keywords
- polymerization
- polymer
- binder
- prepared
- meth
- 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.)
- Abandoned
Links
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- 238000005520 cutting process Methods 0.000 description 1
- 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
- 230000006866 deterioration 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
- WVDDGKGOMKODPV-OCAPALNOSA-N dideuterio(phenyl)methanol Chemical compound [2H][13C]([2H])(O)C1=CC=CC=C1 WVDDGKGOMKODPV-OCAPALNOSA-N 0.000 description 1
- 150000001993 dienes Chemical class 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
- 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
- 206010016256 fatigue Diseases 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000011049 filling 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
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 230000010354 integration 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
- DNHVXYDGZKWYNU-UHFFFAOYSA-N lead;hydrate Chemical compound O.[Pb] DNHVXYDGZKWYNU-UHFFFAOYSA-N 0.000 description 1
- 229920001427 mPEG Polymers 0.000 description 1
- 229920002521 macromolecule 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
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 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
- 238000002156 mixing Methods 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
- 239000001120 potassium sulphate Substances 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
- 150000003254 radicals Chemical class 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000009467 reduction Effects 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
- 230000007017 scission Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 238000010517 secondary 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
- 230000003335 steric effect Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 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
- 238000002076 thermal analysis method Methods 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 238000006276 transfer reaction Methods 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 230000000007 visual effect Effects 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)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Sealing Material Composition (AREA)
- Graft Or Block Polymers (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102008000914.8 | 2008-04-01 | ||
| DE102008000914A DE102008000914A1 (de) | 2008-04-01 | 2008-04-01 | Verfahren zur Synthese von verbesserten Bindemitteln und veränderter Taktizität |
| PCT/EP2009/051117 WO2009121640A1 (de) | 2008-04-01 | 2009-02-02 | Verfahren zur synthese von verbesserten bindemitteln und veränderter taktizität |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2719850A1 true CA2719850A1 (en) | 2009-10-08 |
Family
ID=40591976
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2719850A Abandoned CA2719850A1 (en) | 2008-04-01 | 2009-02-02 | Synthesis of improved binders and modified tacticity |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US8426497B2 (enExample) |
| EP (1) | EP2276817A1 (enExample) |
| JP (1) | JP5634982B2 (enExample) |
| CN (1) | CN101550310B (enExample) |
| BR (1) | BRPI0910448A2 (enExample) |
| CA (1) | CA2719850A1 (enExample) |
| DE (1) | DE102008000914A1 (enExample) |
| RU (1) | RU2010144330A (enExample) |
| TW (1) | TWI498390B (enExample) |
| WO (1) | WO2009121640A1 (enExample) |
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 |
| US11970641B2 (en) | 2017-03-02 | 2024-04-30 | 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 |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE190433C (enExample) | ||||
| US4529787A (en) | 1982-06-15 | 1985-07-16 | S. C. Johnson & Son, Inc. | Bulk polymerization process for preparing high solids and uniform copolymers |
| US4546160A (en) * | 1984-02-29 | 1985-10-08 | S. C. Johnson & Son, Inc. | Bulk polymerization process for preparing high solids and uniform copolymers |
| JP2582510B2 (ja) * | 1992-07-10 | 1997-02-19 | 株式会社日本触媒 | アクリル系重合体の製造方法 |
| US6160059A (en) | 1996-07-26 | 2000-12-12 | Cook Composites And Polymers Co. | Bulk polymerization process for preparing solid acrylic resin |
| WO1998004593A1 (en) | 1996-07-26 | 1998-02-05 | Henkel Corporation | Solid acrylic resin using a continuous tube reactor |
| DE19638094A1 (de) | 1996-09-18 | 1998-03-19 | Basf Ag | Verfahren zur Herstellung von Methylmethacrylat-Polymeren in einem Kreislaufreaktor |
| CA2307665A1 (en) * | 1997-10-31 | 1999-05-14 | Cognis Corporation | Continuous bulk polymerization process |
| JP3628518B2 (ja) * | 1998-07-14 | 2005-03-16 | 三菱レイヨン株式会社 | メタクリル系重合体およびその製造方法 |
| JP2000034303A (ja) * | 1998-07-21 | 2000-02-02 | Mitsubishi Rayon Co Ltd | メタクリル系重合体の製造方法 |
| US20030134949A1 (en) * | 2001-07-17 | 2003-07-17 | Brown Ward Thomas | Wear-resistant coating composition and method for producing a coating |
| DE10149015B4 (de) | 2001-10-04 | 2005-04-14 | Basf Coatings Ag | Verfahren zur kontinuierlichen Polymerisation in Masse und Taylorreaktor für seine Durchführung |
| DE10312509A1 (de) | 2003-03-20 | 2004-09-30 | Basf Ag | Verfahren zur Herstellung von Polymeren mit iso- oder syndiotaktischen Bereichen |
| DE102004001599A1 (de) | 2004-01-09 | 2005-08-04 | Röhm GmbH & Co. KG | Verfahren zur Herstellung von Schmelzpolymerisaten im Rohrreaktor |
| JP4325475B2 (ja) * | 2004-04-27 | 2009-09-02 | Ｄｉｃ株式会社 | メタクリル系重合体及びその製造方法 |
| DE102005001802A1 (de) | 2004-09-30 | 2006-04-06 | List Holding Ag | Verfahren zur kontinuierlichen Durchführung von Polymerisationsprozessen |
| WO2007087465A2 (en) | 2006-01-24 | 2007-08-02 | Intertape Polymer Corp. | Continuous bulk polymerization in a planetary roller extruder |
| DE102006015541A1 (de) | 2006-03-31 | 2007-10-04 | List Holding Ag | Verfahren und Vorrichtung zur Behandlung von zähviskosen Produkten |
-
2008
- 2008-04-01 DE DE102008000914A patent/DE102008000914A1/de not_active Withdrawn
-
2009
- 2009-02-02 WO PCT/EP2009/051117 patent/WO2009121640A1/de not_active Ceased
- 2009-02-02 BR BRPI0910448A patent/BRPI0910448A2/pt not_active IP Right Cessation
- 2009-02-02 JP JP2011502306A patent/JP5634982B2/ja active Active
- 2009-02-02 RU RU2010144330/05A patent/RU2010144330A/ru unknown
- 2009-02-02 EP EP09728210A patent/EP2276817A1/de not_active Ceased
- 2009-02-02 US US12/864,363 patent/US8426497B2/en not_active Expired - Fee Related
- 2009-02-02 CA CA2719850A patent/CA2719850A1/en not_active Abandoned
- 2009-03-27 TW TW098110167A patent/TWI498390B/zh active
- 2009-03-31 CN CN200910132534.9A patent/CN101550310B/zh active Active
Also Published As
| Publication number | Publication date |
|---|---|
| US8426497B2 (en) | 2013-04-23 |
| DE102008000914A1 (de) | 2009-10-08 |
| BRPI0910448A2 (pt) | 2015-09-29 |
| TW201006897A (en) | 2010-02-16 |
| TWI498390B (zh) | 2015-09-01 |
| CN101550310B (zh) | 2014-10-22 |
| EP2276817A1 (de) | 2011-01-26 |
| JP5634982B2 (ja) | 2014-12-03 |
| RU2010144330A (ru) | 2012-05-10 |
| JP2011518238A (ja) | 2011-06-23 |
| HK1138309A1 (en) | 2010-08-20 |
| WO2009121640A1 (de) | 2009-10-08 |
| CN101550310A (zh) | 2009-10-07 |
| US20100298466A1 (en) | 2010-11-25 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FZDE | Discontinued |
Effective date: 20130204 |