JP5558808B2 - ハイソリッドの非水系分散液のクリアコート塗料組成物 - Google Patents
ハイソリッドの非水系分散液のクリアコート塗料組成物 Download PDFInfo
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- JP5558808B2 JP5558808B2 JP2009506700A JP2009506700A JP5558808B2 JP 5558808 B2 JP5558808 B2 JP 5558808B2 JP 2009506700 A JP2009506700 A JP 2009506700A JP 2009506700 A JP2009506700 A JP 2009506700A JP 5558808 B2 JP5558808 B2 JP 5558808B2
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- functional polymer
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- polymer
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- 239000000047 product Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000007870 radical polymerization initiator Substances 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 239000007962 solid dispersion Substances 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 238000007614 solvation Methods 0.000 description 1
- 238000000935 solvent evaporation Methods 0.000 description 1
- 235000015096 spirit Nutrition 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000007592 spray painting technique Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000010189 synthetic method Methods 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
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000001029 thermal curing Methods 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene Substances 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
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
Description
この段落における説明は、単に本発明に関する背景情報を提供し、かつ先行技術を構成しない。
本発明は、ハイソリッドの非水系分散液のクリアコートに関する。該非水系分散液は、分散相及び連続相を含有する。さらにクリアコート組成物は、カルバメート官能性ポリマー、ヒドロキシル官能性ポリマー、硬化剤、及び弱い非極性溶剤を含む。一般に、弱い非極性溶剤は、連続相の一部として存在する。カルバメート官能性ポリマー及びヒドロキシル官能性ポリマーは、典型的に分散相に位置するが、そうでなくてもよく、又は連続相中に存在してもよい。硬化剤、例えばアミノプラスト及びブロックトイソシアネート硬化剤は、一般に連続相に位置するが、分散相の中に位置していてもよい。
次の記載は、単に例示をする性質のものであって、本発明、その応用、もしくは使用の制限を意図しない。
Claims (9)
- 塗料がハイソリッドである、ハイソリッドで非水系分散液のクリアコート塗料組成物であって、分散相及び連続相を含有し、さらに、
i) a)カルバメート官能性ポリマー、b)ヒドロキシル官能性ポリマー、c)アミノプラスト樹脂及びブロックトポリイソシアネートからなる群から選択される硬化剤、並びに、d)10ヒルデブランド未満の溶解パラメータδを有する溶剤を含有し、ここで、前記連続相は前記溶剤を含むか;又は、
ii) a)第1のカルバメート官能性ポリマー、b)第2のカルバメート官能性ポリマー、c)アミノプラスト樹脂及びブロックトポリイソシアネートからなる群から選択される硬化剤、並びに、d)10ヒルデブランド未満の溶解パラメータδを有する溶剤を含有し、ここで、前記分散相は、前記第1のカルバメート官能性ポリマーを含み、前記分散相は前記連続相中に分散されており、かつ、前記連続相は、前記硬化剤、前記第2のカルバメート官能性ポリマー、及び前記溶剤を含むか;又は、
iii) a)アミノプラスト樹脂及びブロックトポリイソシアネートからなる群から選択される硬化剤、b)10ヒルデブランド未満の溶解パラメータδを有する溶剤、並びにc)前記硬化剤と反応するポリマーを含有し、ここで、前記分散相は、前記硬化剤及び前記硬化剤と反応するポリマーを含み、前記分散相は、前記連続相中に分散されており、前記連続相は、前記溶剤を含み、かつ、前記硬化剤と反応するポリマーがカルバメート官能性ポリマーを含む、クリアコート塗料組成物であって、
a.前記クリアコート塗料組成物が少なくとも57質量%の固体含量を有すること、
b.前記分散相中に存在する官能性ポリマーは、その数平均分子量M n が6000〜100000ダルトンであること、
c.前記分散相中に存在する官能性ポリマーの極性が、当該官能性ポリマーが前記連続相中に存在する溶剤に溶解するのを妨げるために十分であること、及び
d.前記のカルバメート官能性の基は、以下の構造:
を特徴とする、クリアコート塗料組成物。 - 前記(i)の場合に、前記の連続相が、さらに硬化剤を含有する、請求項1に記載のクリアコート塗料組成物。
- 前記(i)の場合に、
(A) 前記カルバメート官能性ポリマーa)が、前記分散相中に存在し、かつ
前記ヒドロキシル官能性ポリマーb)が、前記連続相中に存在するか、又は
(B) 前記カルバメート官能性ポリマーa)及び前記ヒドロキシル官能性ポリマーb)が、前記分散相中に存在するか、又は
(C) 前記ヒドロキシル官能性ポリマーb)が、前記分散相中に存在し、かつ
カルバメート官能性樹脂が、前記連続相中に存在する、
請求項2に記載のクリアコート塗料組成物。 - 前記(B)の場合に、さらに、前記連続相中に存在するヒドロキシル官能性ポリマーを含有する、請求項3に記載のクリアコート塗料組成物。
- 前記分散相中に存在する官能性ポリマーは、その数平均分子量M n が10000〜25000ダルトンである、請求項1に記載のクリアコート塗料組成物。
- 前記(i)の場合に、前記硬化剤が、前記溶剤に可溶なメラミン樹脂を含有する、請求項1に記載のクリアコート塗料組成物。
- 前記(i)の場合に、クリアコート塗料組成物3.785リットル(1ガロン)当たりの揮発性有機溶剤の揮発性有機物含量が1.453キログラム(3.2ポンド)未満である、請求項1に記載のクリアコート塗料組成物。
- 前記(i)の場合に、クリアコート塗料組成物3.785リットル(1ガロン)当たりの揮発性有機溶剤の揮発性有機物含量が1.362キログラム(3.0ポンド)未満である、請求項1に記載のクリアコート塗料組成物。
- 前記(i)の場合に、前記溶剤が、VM&Pナフサを含有する、請求項1に記載のクリアコート塗料組成物。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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US11/379,615 | 2006-04-21 | ||
US11/379,615 US8318849B2 (en) | 2006-04-21 | 2006-04-21 | High solids nonaqueous dispersion clearcoats |
PCT/US2007/066683 WO2007124290A1 (en) | 2006-04-21 | 2007-04-16 | High solids nonaqueous dispersion clearcoats |
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JP2009534505A JP2009534505A (ja) | 2009-09-24 |
JP5558808B2 true JP5558808B2 (ja) | 2014-07-23 |
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JP2009506700A Expired - Fee Related JP5558808B2 (ja) | 2006-04-21 | 2007-04-16 | ハイソリッドの非水系分散液のクリアコート塗料組成物 |
Country Status (6)
Country | Link |
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US (1) | US8318849B2 (ja) |
EP (1) | EP2035509B8 (ja) |
JP (1) | JP5558808B2 (ja) |
AT (1) | ATE520747T1 (ja) |
CA (1) | CA2618226A1 (ja) |
WO (1) | WO2007124290A1 (ja) |
Families Citing this family (4)
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US20110097482A1 (en) * | 2009-10-27 | 2011-04-28 | Basf Coatings Ag | Compact coating system and process |
CN102134439A (zh) * | 2011-02-25 | 2011-07-27 | 上海富臣化工有限公司 | 低温烘烤型pu双组分塑胶漆及其制备方法 |
EP3124515A1 (de) * | 2015-07-28 | 2017-02-01 | Evonik Degussa GmbH | Reaktive nicht wässrige dispersionen für lacke, kleb- und dichtstoffe |
CN109401585A (zh) * | 2018-09-30 | 2019-03-01 | 湖北零柒实业有限责任公司 | 一种军用纽扣涂料 |
Family Cites Families (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2979514A (en) | 1957-07-16 | 1961-04-11 | Rohm & Haas | Process for preparing carbonatoalkyl acrylates and methacrylates |
US3479328A (en) | 1966-11-18 | 1969-11-18 | Ashland Oil Inc | Novel monomers and polymers |
US3674838A (en) | 1969-06-05 | 1972-07-04 | Ashland Oil Inc | Vinyl carbamyloxy carboxylates |
US4126747A (en) | 1976-12-28 | 1978-11-21 | Union Carbide Corporation | Carbamoyloxy acrylate compounds |
US4301257A (en) | 1979-05-18 | 1981-11-17 | Akzona Incorporated | Polyfunctional isocyanates free of alkali and urea groups |
US4279833A (en) | 1979-12-17 | 1981-07-21 | Ashland Chemical Company | Acrylic monomers containing carbamate functionality |
US4340497A (en) | 1980-03-21 | 1982-07-20 | Union Carbide Corporation | (N-Substituted carbamoyloxy) alkanoyloxyalkyl acrylate esters |
US4758632A (en) | 1984-02-17 | 1988-07-19 | American Cyanamid Company | Self-cross-linkable acrylic polymer containing hydroxyalkyl carbamate groups and coating compositions containing the same |
US4818792A (en) | 1985-04-29 | 1989-04-04 | Basf Corporation | Stabilized high solids low Ig copolymer nonaqueous dispersion for clear coat finishes |
WO1993004097A1 (en) * | 1991-08-23 | 1993-03-04 | Exxon Chemical Patents, Inc. | Adhesive acrylic copolymers with a broad molecular weight distribution |
JP2672031B2 (ja) * | 1992-10-30 | 1997-11-05 | ピーピージー インダストリーズ,インコーポレイテッド | 耐酸エッチング性を有する塗膜を与えるアミノプラスト硬化可能な塗膜形成組成物 |
JP3276152B2 (ja) * | 1994-04-29 | 2002-04-22 | ピーピージー インダストリーズ オハイオ, インコーポレイテッド | 酸エッチング耐性を有する塗膜を提供する柔軟性アミノプラスト硬化性塗膜形成組成物 |
US5593785A (en) * | 1995-06-26 | 1997-01-14 | Ppg Industries, Inc. | Coating compositions containing acrylic polymers with pendant carbamate groups exhibiting improved intercoat adhesion |
US5747590A (en) * | 1996-12-04 | 1998-05-05 | E. I. Du Pont De Nemours And Company | Acrylic-melamine-functionalized oligomer coating composition |
CA2249705C (en) * | 1997-11-12 | 2006-09-12 | Basf Corporation | High solids thermosetting compositions with dual cure mechanism |
JPH11158342A (ja) * | 1997-11-25 | 1999-06-15 | Nippon Paint Co Ltd | 硬化性樹脂組成物 |
BR0013169A (pt) | 1999-09-30 | 2002-05-28 | Basf Corp | Resinas carbamato-funcional possuindo adesão aperfeiçoada, processo para fabricação das mesmas e processo para aperfeiçoar a adesão inter-revestimento |
US6916877B2 (en) | 2000-06-16 | 2005-07-12 | Basf Corporation | Coating composition including a water-based copolymer cross-linking with a water-dispersible cross-linking agent, method of preparing the same, and a cured film thereof |
US6541577B2 (en) * | 2000-12-06 | 2003-04-01 | Basf Corporation | Carbamate functional polymers and oligomers |
US7321013B2 (en) | 2000-12-19 | 2008-01-22 | Basf Corporation | Method for obtaining coating compositions having reduced VOC |
DE10129969A1 (de) * | 2001-06-21 | 2003-01-09 | Basf Coatings Ag | Carbamat- und/oder Allophanatgruppen enthaltende, thermisch und mit aktinischer Strahlung härtbare Gemische |
DE10147546B4 (de) | 2001-09-26 | 2006-04-13 | Basf Coatings Ag | Polyurethan, Verfahren zu seiner Herstellung und seine Verwendung |
US6995208B2 (en) * | 2001-12-11 | 2006-02-07 | Basf Corporation | Clearcoat composition for primerless MVSS adhesion |
US20040087728A1 (en) | 2002-10-31 | 2004-05-06 | Donald Campbell | Carbamate functional addition polymers and a method for their preparation |
US20050074617A1 (en) * | 2003-10-02 | 2005-04-07 | Jun Lin | Clearcoat composition having both windshield sealant and recoat adhesion |
US20050238899A1 (en) | 2004-04-27 | 2005-10-27 | Isao Nagata | High solids clearcoat compositions containing silane functional compounds |
US7838078B2 (en) * | 2004-08-30 | 2010-11-23 | E. I. Du Pont De Nemours And Company | Clearcoat composition compatible with both waterborne and solventborne basecoats |
US7871669B2 (en) * | 2004-08-30 | 2011-01-18 | E.I. Du Pont De Nemours And Company | Method for achieving a durable two-tone finish on a vehicle |
-
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- 2007-04-16 CA CA002618226A patent/CA2618226A1/en not_active Abandoned
- 2007-04-16 AT AT07760692T patent/ATE520747T1/de not_active IP Right Cessation
- 2007-04-16 WO PCT/US2007/066683 patent/WO2007124290A1/en active Application Filing
- 2007-04-16 EP EP07760692A patent/EP2035509B8/en not_active Not-in-force
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JP2009534505A (ja) | 2009-09-24 |
EP2035509A1 (en) | 2009-03-18 |
US20070249777A1 (en) | 2007-10-25 |
CA2618226A1 (en) | 2007-11-01 |
US8318849B2 (en) | 2012-11-27 |
ATE520747T1 (de) | 2011-09-15 |
EP2035509B1 (en) | 2011-08-17 |
EP2035509B8 (en) | 2012-02-08 |
WO2007124290A1 (en) | 2007-11-01 |
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