JP2012514094A - 分岐型のリン含有樹脂を有するコーティング組成物 - Google Patents
分岐型のリン含有樹脂を有するコーティング組成物 Download PDFInfo
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- JP2012514094A JP2012514094A JP2011544424A JP2011544424A JP2012514094A JP 2012514094 A JP2012514094 A JP 2012514094A JP 2011544424 A JP2011544424 A JP 2011544424A JP 2011544424 A JP2011544424 A JP 2011544424A JP 2012514094 A JP2012514094 A JP 2012514094A
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- 238000003379 elimination reaction Methods 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 150000002118 epoxides Chemical class 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- RJUVPCYAOBNZAX-VOTSOKGWSA-N ethyl (e)-3-(dimethylamino)-2-methylprop-2-enoate Chemical compound CCOC(=O)C(\C)=C\N(C)C RJUVPCYAOBNZAX-VOTSOKGWSA-N 0.000 description 1
- XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical compound CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 description 1
- SLAFUPJSGFVWPP-UHFFFAOYSA-M ethyl(triphenyl)phosphanium;iodide Chemical compound [I-].C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(CC)C1=CC=CC=C1 SLAFUPJSGFVWPP-UHFFFAOYSA-M 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- CATSNJVOTSVZJV-UHFFFAOYSA-N heptan-2-one Chemical compound CCCCCC(C)=O CATSNJVOTSVZJV-UHFFFAOYSA-N 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-M hexanoate Chemical compound CCCCCC([O-])=O FUZZWVXGSFPDMH-UHFFFAOYSA-M 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- YAMHXTCMCPHKLN-UHFFFAOYSA-N imidazolidin-2-one Chemical compound O=C1NCCN1 YAMHXTCMCPHKLN-UHFFFAOYSA-N 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 239000006115 industrial coating Substances 0.000 description 1
- 239000003317 industrial substance Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- 230000001788 irregular 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
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000009533 lab test Methods 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- MOUPNEIJQCETIW-UHFFFAOYSA-N lead chromate Chemical compound [Pb+2].[O-][Cr]([O-])(=O)=O MOUPNEIJQCETIW-UHFFFAOYSA-N 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 150000004712 monophosphates Chemical class 0.000 description 1
- DILRJUIACXKSQE-UHFFFAOYSA-N n',n'-dimethylethane-1,2-diamine Chemical compound CN(C)CCN DILRJUIACXKSQE-UHFFFAOYSA-N 0.000 description 1
- LSHROXHEILXKHM-UHFFFAOYSA-N n'-[2-[2-[2-(2-aminoethylamino)ethylamino]ethylamino]ethyl]ethane-1,2-diamine Chemical compound NCCNCCNCCNCCNCCN LSHROXHEILXKHM-UHFFFAOYSA-N 0.000 description 1
- SWVGZFQJXVPIKM-UHFFFAOYSA-N n,n-bis(methylamino)propan-1-amine Chemical compound CCCN(NC)NC SWVGZFQJXVPIKM-UHFFFAOYSA-N 0.000 description 1
- BXYVQNNEFZOBOZ-UHFFFAOYSA-N n-[3-(dimethylamino)propyl]-n',n'-dimethylpropane-1,3-diamine Chemical compound CN(C)CCCNCCCN(C)C BXYVQNNEFZOBOZ-UHFFFAOYSA-N 0.000 description 1
- WHIVNJATOVLWBW-UHFFFAOYSA-N n-butan-2-ylidenehydroxylamine Chemical compound CCC(C)=NO WHIVNJATOVLWBW-UHFFFAOYSA-N 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- KYTZHLUVELPASH-UHFFFAOYSA-N naphthalene-1,2-dicarboxylic acid Chemical compound C1=CC=CC2=C(C(O)=O)C(C(=O)O)=CC=C21 KYTZHLUVELPASH-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 239000004843 novolac epoxy resin Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- NDLPOXTZKUMGOV-UHFFFAOYSA-N oxo(oxoferriooxy)iron hydrate Chemical compound O.O=[Fe]O[Fe]=O NDLPOXTZKUMGOV-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000026731 phosphorylation Effects 0.000 description 1
- 238000005554 pickling Methods 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920001281 polyalkylene Polymers 0.000 description 1
- 229920001610 polycaprolactone Polymers 0.000 description 1
- 239000004632 polycaprolactone Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920000137 polyphosphoric acid Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920000909 polytetrahydrofuran Polymers 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 239000013615 primer Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229940005657 pyrophosphoric acid Drugs 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000007761 roller coating Methods 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- NVKTUNLPFJHLCG-UHFFFAOYSA-N strontium chromate Chemical compound [Sr+2].[O-][Cr]([O-])(=O)=O NVKTUNLPFJHLCG-UHFFFAOYSA-N 0.000 description 1
- 229960002317 succinimide Drugs 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
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- CCIYPTIBRAUPLQ-UHFFFAOYSA-M tetrabutylphosphanium;iodide Chemical compound [I-].CCCC[P+](CCCC)(CCCC)CCCC CCIYPTIBRAUPLQ-UHFFFAOYSA-M 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 239000012974 tin catalyst Substances 0.000 description 1
- RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical compound OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- 150000004072 triols Chemical class 0.000 description 1
- 125000002264 triphosphate group Chemical class [H]OP(=O)(O[H])OP(=O)(O[H])OP(=O)(O[H])O* 0.000 description 1
- AVWRKZWQTYIKIY-UHFFFAOYSA-N urea-1-carboxylic acid Chemical compound NC(=O)NC(O)=O AVWRKZWQTYIKIY-UHFFFAOYSA-N 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003739 xylenols Chemical class 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
- C09D5/44—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes for electrophoretic applications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/14—Polycondensates modified by chemical after-treatment
- C08G59/1405—Polycondensates modified by chemical after-treatment with inorganic compounds
- C08G59/1422—Polycondensates modified by chemical after-treatment with inorganic compounds containing phosphorus
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/14—Polycondensates modified by chemical after-treatment
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/14—Polycondensates modified by chemical after-treatment
- C08G59/1433—Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds
- C08G59/1488—Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds containing phosphorus
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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
- 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
- C09D163/00—Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins
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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
- 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
- C09D5/24—Electrically-conducting paints
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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
- 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
- C09D5/44—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes for electrophoretic applications
- C09D5/4419—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes for electrophoretic applications with polymers obtained otherwise than by polymerisation reactions only involving carbon-to-carbon unsaturated bonds
- C09D5/443—Polyepoxides
- C09D5/4434—Polyepoxides characterised by the nature of the epoxy binder
- C09D5/4438—Binder based on epoxy/amine adducts, i.e. reaction products of polyepoxides with compounds containing amino groups only
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- General Chemical & Material Sciences (AREA)
- Polymers & Plastics (AREA)
- Wood Science & Technology (AREA)
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- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Inorganic Chemistry (AREA)
- Paints Or Removers (AREA)
Abstract
Description
この箇所の記載は、単に、本開示に関連した情報を提供するだけで、先行技術を成さないこともある。
リン酸塩処理されていない金属の基材(すなわち、リン酸塩前処理されていない金属の基材)であってよい金属の基材上に電着コーティングを電着する組成物及び方法であって、その電着コーティングが優れた腐蝕保護を提供するものが開示される。リン酸塩前処理法のための工程及び装置の排除により、新たな塗装作業場の構築における主要なコスト削減を可能にし、目下の自動車生産プラントにおける塗装作業場の運転での簡素化とコスト削減とを可能とする。
以下の詳細な説明は、単に例示を性質とするものであり、本開示、用途もしくは使用を制限することを意図するものではない。
調製物A: 分岐型のリン酸化エポキシ樹脂の製造
撹拌機と還流凝縮器を備えた反応器に、25.85質量部のノルマルブタノール、10.20質量部のエチレングリコールモノブチルエーテル及び55.62質量部のビスフェノールAのジグリシジルエーテルを装填する。該反応器の内容物を、約15分間撹拌し、引き続き3.11部のジエタノールアミンを添加する。得られた混合物を77゜F(25℃)に加熱し、次いで加熱を中止し、そして反応混合物を発熱状態にさせる。反応温度は、120.2〜122゜F(49〜50℃)にまで上がり続ける。該反応混合物を、140〜149゜F(60〜65℃)で30分間保持する。該反応器に、4.261質量部のリン酸(75%水性)及び1.77質量部のノルマルブタノールの混合物を添加する。その添加の間に、温度は、102.2゜F(49℃)未満に保持する。該反応混合物を、約15分にわたり撹拌し、次いで該反応器を220〜250゜F(104.4〜121.1℃)に加熱する。反応は、生成物のエポキシ当たりの質量が800又はそれより高くなるまで継続させる。次いで、脱イオン水を、0.899質量部の第一の部で添加し、該反応混合物を、220〜250゜F(104.4〜121.1℃)で1時間にわたり保持する。脱イオン水の第二の部、すなわち0.70質量部を、次いで該反応混合物に添加する。再び反応混合物を、220〜250゜F(104.4〜121.1℃)で1時間にわたり保持する。脱イオン水の最後の部、すなわち0.70質量部を、次いで該反応混合物に添加する。再び反応混合物を、220〜250゜F(104.4〜121.1℃)で1時間にわたり保持する。生成物を、次いでノルマルブタノールで72質量部の非揮発性物質にまで希釈する。
付属の加熱マントルを有する5Lのフラスコ中で、以下の材料:ビスフェノールAのジグリシジルエーテル(DGEBA)(18.03部)、ビスフェノールA(BPA)(4.1部)、フェノール(1.41部)及びプロピレングリコール n−ブチルエーテル(0.36部)を合する。
EP0505445号B1に従って、有機粉砕樹脂水溶液を、第一段階で2598部のビスフェノールAグリシジルエーテル(エポキシ当量(EEW)188g/当量)、787部のビスフェノールA、603部のドデシルフェノール及び206部のブチルグリコールをステンレス鋼反応容器中で4部のトリフェニルホスフィンの存在下で130℃でEEW(エポキシ当量)が865g/当量に到達するまで反応させることによって製造する。冷却の過程で、そのバッチを、849部のブチルグリコール及び1534部のD.E.R(登録商標)732(ポリプロピレングリコールジグリシジルエーテル、DOW Chemical,米国)で希釈し、そしてさらに90℃で266部の2,2′−アミノエトキシエタノール及び212部のN,N−ジメチルアミノプロピルアミンと反応させる。2時間後に、樹脂溶液の粘度は、一定である(5.3dPas;SOLVENON(登録商標)PM(メトキシプロパノール、BASF(ドイツ))中40%;コーン・プレート粘度計で23℃)。それを、1512部のブチルグリコールで希釈し、そしてベースの基は、201部の氷酢酸で部分的に中和され、そして該生成物をさらに1228部の脱イオン水で希釈し、排出させる。それにより、60%濃度の有機樹脂水溶液であって、その10%希釈がpH6.0を有する溶液が得られる。該樹脂溶液は、ペースト製造のために直接的に使用する。
まず、125部の水と594部の調製物Bの粉砕樹脂からプレミックスを形成する。次いで、7部の酢酸、9部のTetronic(登録商標)901、8部のカーボンブラック、547部の二酸化チタンTI−PURE(登録商標)R900(DuPont、米国)、44部のジ−n−ブチルスズオキシド、47部の次サリチル酸ビスマス及び120部のASP200クレイ(Langer&Co./ドイツ)を添加する。該混合物を、高速溶解撹拌機で30分にわたり予備分散させる。該混合物を引き続き、小さい研究室用のミル(Motor Mini Mill,Eiger Engineering Ltd,英国)中で、それが12μm未満又はそれに等しいヘグマン粒度を測定するまで分散させ、そして固体含有率を追加の水で調整する。得られた顔料ペーストは、固体含有率:67質量%(110℃で1時間)を有する。
1096.1部の調製物Bと、147.3部の調製物Dと、1256.6部の脱イオン水とを合することによって浴を調製した。水・調製物Bの樹脂エマルジョンを一定の撹拌をしつつ1つの容器中で合し、そして調製物Dを撹拌しながら添加する。前記浴の固体含有率は、19質量%である。
対照パネルを、実施例1について記載される通りであるが、U32AD500(BASF Corporationにより販売される市販品)を使用して製造した。
統合プロセスSB(溶剤系):
− U28AU227(BASF Corporationにより販売される市販品)を0.9ミルまで適用し、引き続き5分間室温でフラッシングする
− E38WU466L(BASF Corporationにより販売される市販品)を0.9ミルまで適用し、引き続き8分間室温でフラッシングする
− R10CG392(BASF Corporationにより販売される市販品)を1.8ミルまで適用し、引き続き8分間室温でフラッシングし、引き続き5分間200゜Fでフラッシングし、引き続き17分間285゜Fでフラッシングする
− U28WW554(BASF Corporationにより販売される市販品)を1.0ミルまで適用し、5分間室温でフラッシングし、引き続き30分間265゜Fでフラッシングする
− E54WW301(BASF Corporationにより販売される市販品)を0.5ミルまで適用し、5分間150゜Fでフラッシングする
− E211WW328(BASF Corporationにより販売される市販品)を0.4ミルまで適用し、5分間150゜Fでフラッシングする
− E10CG081(BASF Corporationにより販売される市販品)を1.8ミルまで適用し、10分間室温でフラッシングし、引き続き10分間180゜Fでフラッシングし、25分間255゜Fでフラッシングする
− 960KM0002(BASF Corporationにより販売される市販品)を2.0ミルまで適用し、20分340゜Fで硬化させる
Claims (15)
- バインダーを含む水性のカソード電着可能なコーティング組成物であって、前記バインダーが分岐型のリン酸化エポキシ樹脂を含む前記コーティング組成物。
- 前記分岐型のリン酸化エポキシ樹脂がアミン官能性である、請求項1又は2に記載の水性のカソード電着可能なコーティング組成物。
- 前記分岐型のリン酸化樹脂が、一リン酸エステル基、一ホスホン酸エステル基、二リン酸エステル基、二ホスホン酸エステル基又はその組み合わせを含む、請求項1から3までのいずれか1項に記載の水性のカソード電着可能なコーティング組成物。
- 前記分岐型のリン酸化樹脂が、平均で、1分子当たり1個より多くのリン原子を含む、請求項1から4までのいずれか1項に記載の水性のカソード電着可能なコーティング組成物。
- 前記コーティング組成物がリン酸化エポキシ樹脂以外のエポキシ樹脂を含まず、かつ該リン酸化エポキシ樹脂がアミン官能性である、請求項1から5までのいずれか1項に記載の水性のカソード電着可能なコーティング組成物。
- 前記バインダーが、約0.01〜約99質量%の分岐型のリン酸化樹脂、好ましくは少なくとも約5質量%の分岐型のリン酸化樹脂を含む、請求項1から6までのいずれか1項に記載の水性のカソード電着可能なコーティング組成物。
- 前記分岐型のリン酸化エポキシ樹脂が、ビスフェノールAを基礎とするものである、請求項1から7までのいずれか1項に記載の水性のカソード電着可能なコーティング組成物。
- 前記バインダーが、更に、第二のアミン官能性樹脂を含む、請求項1から8までのいずれか1項に記載の水性のカソード電着可能なコーティング組成物。
- 前記リン酸化樹脂が、三リン酸エステル基を含む、請求項1から9までのいずれか1項に記載の水性のカソード電着可能なコーティング組成物。
- 更に、前記分岐型のエポキシ樹脂と反応性の架橋剤を含む、請求項1から10までのいずれか1項に記載の水性のカソード電着可能なコーティング組成物。
- 更に、前記架橋剤と反応性の第二のアミン官能性樹脂を含み、その際、該第二のアミン官能性の樹脂が、リン含有基を含まない、請求項11に記載の水性のカソード電着可能なコーティング組成物。
- 金属の自動車車体をコーティングする方法であって、
(a)金属の自動車車体を清浄化することと、
(b)清浄化した金属の自動車車体を、請求項1から12までのいずれか1項に記載の水性のコーティング組成物中に入れることと、
(c)前記金属の自動車車体をカソードとして電気回路に接続し、そして前記水性のコーティング組成物に電流を流して、前記金属の自動車車体上にコーティング層を析出させることと、
を含む、金属の自動車車体をコーティングする方法。 - 前記金属の自動車車体が、リン酸塩前処理されていない、請求項13に記載の導電性の基材のコーティング方法。
- 請求項13又は14に記載の方法により製造されるコーティングされた基材。
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US12/344,902 | 2008-12-29 | ||
US12/344,902 US9206284B2 (en) | 2008-12-29 | 2008-12-29 | Coating compositions with branched phosphorous-containing resin |
PCT/US2009/048640 WO2010077381A1 (en) | 2008-12-29 | 2009-06-25 | Coating compositions with branched phosphorous-containing resin |
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EP (1) | EP2379615B1 (ja) |
JP (1) | JP5738198B2 (ja) |
KR (1) | KR20110118648A (ja) |
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US10370545B2 (en) * | 2017-09-19 | 2019-08-06 | Ppg Industries Ohio, Inc. | Low VOC anionic electrodepositable coating composition |
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WO2010077381A1 (en) | 2010-07-08 |
EP2379615A1 (en) | 2011-10-26 |
EP2379615B1 (en) | 2014-11-05 |
KR20110118648A (ko) | 2011-10-31 |
US9206284B2 (en) | 2015-12-08 |
US20100163424A1 (en) | 2010-07-01 |
CN102272189A (zh) | 2011-12-07 |
JP5738198B2 (ja) | 2015-06-17 |
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