JP6252714B1 - アクリル変性アルキド樹脂及び無機材料薄膜下塗り用コーティング剤 - Google Patents
アクリル変性アルキド樹脂及び無機材料薄膜下塗り用コーティング剤 Download PDFInfo
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- JP6252714B1 JP6252714B1 JP2017538448A JP2017538448A JP6252714B1 JP 6252714 B1 JP6252714 B1 JP 6252714B1 JP 2017538448 A JP2017538448 A JP 2017538448A JP 2017538448 A JP2017538448 A JP 2017538448A JP 6252714 B1 JP6252714 B1 JP 6252714B1
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- meth
- acrylate
- alkyd resin
- acid
- inorganic material
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- 229920000180 alkyd Polymers 0.000 title claims abstract description 76
- 229910010272 inorganic material Inorganic materials 0.000 title claims abstract description 33
- 239000011147 inorganic material Substances 0.000 title claims abstract description 33
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- 239000000178 monomer Substances 0.000 claims abstract description 37
- 239000011248 coating agent Substances 0.000 claims abstract description 36
- 239000000203 mixture Substances 0.000 claims abstract description 35
- 239000010409 thin film Substances 0.000 claims abstract description 32
- 239000000463 material Substances 0.000 claims abstract description 25
- 229920001577 copolymer Polymers 0.000 claims abstract description 6
- -1 acrylate compound Chemical class 0.000 claims description 85
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 79
- 238000000576 coating method Methods 0.000 claims description 20
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 16
- 229920002554 vinyl polymer Polymers 0.000 claims description 5
- 238000004544 sputter deposition Methods 0.000 claims description 3
- 238000001771 vacuum deposition Methods 0.000 claims description 2
- 239000002994 raw material Substances 0.000 abstract description 11
- 239000004925 Acrylic resin Substances 0.000 abstract description 4
- 229920000178 Acrylic resin Polymers 0.000 abstract description 4
- 239000000470 constituent Substances 0.000 abstract description 2
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- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 14
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- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 6
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- DVVXXHVHGGWWPE-UHFFFAOYSA-N 2-(dimethylamino)benzoic acid Chemical compound CN(C)C1=CC=CC=C1C(O)=O DVVXXHVHGGWWPE-UHFFFAOYSA-N 0.000 description 4
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
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- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- 239000004734 Polyphenylene sulfide Substances 0.000 description 4
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- LZHUBCULTHIFNO-UHFFFAOYSA-N 2,4-dihydroxy-1,5-bis[4-(2-hydroxyethoxy)phenyl]-2,4-dimethylpentan-3-one Chemical compound C=1C=C(OCCO)C=CC=1CC(C)(O)C(=O)C(O)(C)CC1=CC=C(OCCO)C=C1 LZHUBCULTHIFNO-UHFFFAOYSA-N 0.000 description 3
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- 238000001556 precipitation Methods 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 230000001846 repelling effect Effects 0.000 description 1
- 229920003987 resole Polymers 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 238000007151 ring opening polymerisation reaction Methods 0.000 description 1
- 238000007761 roller coating Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- ADXGNEYLLLSOAR-UHFFFAOYSA-N tasosartan Chemical compound C12=NC(C)=NC(C)=C2CCC(=O)N1CC(C=C1)=CC=C1C1=CC=CC=C1C=1N=NNN=1 ADXGNEYLLLSOAR-UHFFFAOYSA-N 0.000 description 1
- UFDHBDMSHIXOKF-UHFFFAOYSA-N tetrahydrophthalic acid Natural products OC(=O)C1=C(C(O)=O)CCCC1 UFDHBDMSHIXOKF-UHFFFAOYSA-N 0.000 description 1
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- DXNCZXXFRKPEPY-UHFFFAOYSA-N tridecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCC(O)=O DXNCZXXFRKPEPY-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
- 239000002383 tung oil Substances 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- C08F2/44—Polymerisation in the presence of compounding ingredients, e.g. plasticisers, dyestuffs, fillers
-
- 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
- C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
- C08F283/01—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to unsaturated polyesters
-
- 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
- C08F285/00—Macromolecular compounds obtained by polymerising monomers on to preformed graft polymers
-
- 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
- C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C09D133/10—Homopolymers or copolymers of methacrylic acid esters
-
- 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
- C09D151/00—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
- C09D151/08—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers grafted on to macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
-
- 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
- C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
- C09D167/08—Polyesters modified with higher fatty oils or their acids, or with natural resins or resin acids
-
- 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
- C09D4/00—Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
- C09D4/06—Organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond in combination with a macromolecular compound other than an unsaturated polymer of groups C09D159/00 - C09D187/00
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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
- C09D5/002—Priming paints
Landscapes
- Chemical & Material Sciences (AREA)
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- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Materials Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Paints Or Removers (AREA)
- Laminated Bodies (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Graft Or Block Polymers (AREA)
- Polyesters Or Polycarbonates (AREA)
Abstract
Description
カラム ;東ソー株式会社製 TSKgel 4000HXL、TSKgel 3000HXL、TSKgel 2000HXL、TSKgel 1000HXL
検出器 ;RI(示差屈折計)
データ処理;東ソー株式会社製 GPCワークステーション EcoSEC-WS
測定条件 ;カラム温度 40℃
溶媒 テトラヒドロフラン
流速 0.35ml/分
標準 ;単分散ポリスチレン
試料 ;樹脂固形分換算で0.2質量%のテトラヒドロフラン溶液をマイクロフィルターでろ過したもの(100μl)
重量平均分子量(Mw)、分子量分布(Mw/Mn)は下記条件のゲルパーミュレーションクロマトグラフィー(GPC)により測定した。
カラム ;東ソー株式会社製 TSKgel 4000HXL、TSKgel 3000HXL、TSKgel 2000HXL、TSKgel 1000HXL
検出器 ;RI(示差屈折計)
データ処理;東ソー株式会社製 GPCワークステーション EcoSEC-WS
測定条件 ;カラム温度 40℃
溶媒 テトラヒドロフラン
流速 0.35ml/分
標準 ;単分散ポリスチレン
試料 ;樹脂固形分換算で0.2質量%のテトラヒドロフラン溶液をマイクロフィルターでろ過したもの(100μl)
攪拌棒、温度センサー、精留管を有するフラスコに、脱水ヒマシ油760質量部、ペンタエリスリトール150質量部、トリメチロールプロパン140質量部、無水フタル酸345質量部、無水マレイン酸10質量部を仕込み、乾燥窒素をフラスコ内にフローさせ攪拌しながら210〜230℃に加熱し、脱水縮合反応を行った。酸価が8.0mgKOH/gとなったところで反応を停止し、150℃まで冷却後、酢酸ブチルを滴下して固形分70質量%に希釈して、アルキド樹脂(A−1)溶液を得た。得られたアルキド樹脂(A−1)の油長は60、重量平均分子量(Mw)は10,500、分子量分布(Mw/Mn)は4.5、水酸基価は141mgKOH/g、酸価は8.0mgKOH/gであった。
攪拌棒、温度センサー、精留管を有するフラスコに、亜麻仁油580質量部、ペンタエリスリトール120質量部、グリセリン180質量部、無水フタル酸480質量部を仕込み、乾燥窒素をフラスコ内にフローさせ攪拌しながら210〜230℃に加熱し、脱水縮合反応を行った。酸価が5.0mgKOH/gとなったところで反応を停止し、150℃まで冷却後、酢酸ブチルを滴下して固形分70質量%に希釈して、アルキド樹脂(A−2)溶液を得た。得られたアルキド樹脂(A−2)の油長は50、重量平均分子量(Mw)は9,500、分子量分布(Mw/Mn)は5.6、水酸基価は180mgKOH/g、酸価は5.6mgKOH/gであった。
攪拌棒、温度センサー、コンデンサ、滴下ロートを有するフラスコに、酢酸ブチル326質量部、アルキド樹脂(A−1)714質量部(固形分)を仕込み、乾燥窒素をフラスコ内にフローさせ攪拌しながら80〜90℃に加熱した。滴下ロートにメタクリル酸メチル180質量部、2−ヒドロキシエチルメタクリレート50質量部、スチレン70質量部、及びt−ブチルパーオキシ−2−エチルヘキサノエート10質量部を仕込み、フラスコ中に4時間かけて滴下した。更に80〜90℃で4時間アクリル重合反応を継続し、酢酸ブチルで固形分60質量%に希釈して、アクリル変性アルキド樹脂(1)溶液を得た。得られたアクリル変性アルキド樹脂(1)の油長は42、重量平均分子量(Mw)は25,000、分子量分布(Mw/Mn)は8.5、水酸基価は120mgKOH/g、酸価は7.6mgKOH/gであった。
攪拌棒、温度センサー、コンデンサ、滴下ロートを有するフラスコに、酢酸ブチル326質量部、アルキド樹脂(A−2)714質量部(固形分)を仕込み、乾燥窒素をフラスコ内にフローさせ攪拌しながら80〜90℃に加熱した。滴下ロートにメタクリル酸メチル180質量部、2−ヒドロキシエチルメタクリレート50質量部、スチレン70質量部、及びt−ブチルパーオキシ−2−エチルヘキサノエート10質量部を仕込み、フラスコ中に4時間かけて滴下した。更に80〜90℃で4時間アクリル重合反応を継続し、酢酸ブチルで固形分60質量%に希釈して、アクリル変性アルキド樹脂(2)溶液を得た。得られたアクリル変性アルキド樹脂(2)のの油長は35、重量平均分子量(Mw)は18,000、分子量分布(Mw/Mn)は7.4、水酸基価は145mgKOH/g、酸価は6.0mgKOH/gであった。
攪拌棒、温度センサー、コンデンサを有するフラスコに、酢酸ブチルを410質量部仕込み、80〜90℃に加熱した。滴下ロートに、スチレン160質量部、メチルメタアクリレート20質量部、n−ブチルアクリレート100質量部、4−ヒドロキシブチルアクリレート40質量部、N−(n−ブトキシメチル)アクリルアミド80質量部、重合開始剤としてt−ブチルパーオキシ−2−エチルヘキサノエート10質量部を仕込み、4時間かけて滴下した。更に80〜90℃で4時間アクリル重合反応を継続し、必要に応じて酢酸ブチルを加えることにより固形分50%のアクリル樹脂(1’)溶液を得た。
表1に示す割合で各成分を配合して硬化性組成物を調製し、これについて下記の要領で各種評価を行った。結果を表1に示す。
◆(メタ)アクリレート化合物(X−1):DIC株式会社製「ユニディック V−4000BA」
◆(メタ)アクリレート化合物(X−2):DIC株式会社製「ユニディック V−4001EA」
◆(メタ)アクリレート化合物(X−3):DIC株式会社製「ユニディック V−4025」
◆(メタ)アクリレート化合物(X−4):ジペンタエリスリトールペンタアクリレートとヘキサアクリレートとの混合物(東亞合成株式会社製「アロニックスM−402」)
◆(メタ)アクリレート化合物(X−5):ペンタエリスリトールトリアクリレートとテトラアクリレートとの混合物(東亞合成株式会社製、「アロニックスM−305」)
◆(メタ)アクリレート化合物(X−6):トリメチロールプロパントリアクリレート(TMPTA)(東亞合成株式会社製「アロニックスM−309」)
◆(メタ)アクリレート化合物(X−7):トリプロピレングリコールジアクリレート(東亞合成株式会社製「アロニックスM−220」)
◆(メタ)アクリレート化合物(X−8):トリシクロデカンジメタノールジアクリレート(新中村化学株式会社製「NKエステルA−DCP」)
◆アミノ樹脂:日本サイテックインダストリーズ株式会社製「サイメル303」
◆光重合開始剤(1):BASF社製「イルガキュア651」
◆光重合開始剤(2):BASF社製「イルガキュア184」
◆表面改質剤:DIC株式会社製「メガファックF−477」
プラスチック基材上に硬化性組成物をスプレーガンでスプレー塗装し、80℃で10分間乾燥させた。80W/cmの高圧水銀灯で照射量1000mJ/cm2の紫外線を照射し、プラスチック基材上に指定の膜厚で下塗り層を形成した。次に、下塗り層の表面に真空蒸着装置を用いて100nmのアルミニウム蒸着層を形成し、試験片1〜4を得た。
各試験片のプラスチック基材の種類、及び下塗り層の膜厚は以下の通り。
試験片1:BMC(バルクモールディングコンパウンド)基材、膜厚15〜20μm
試験片2:BMC(バルクモールディングコンパウンド)基材、膜厚45〜50μm
試験片3:ABS(アクリロニトリル−ブタジエン−スチレン共重合樹脂)基材、膜厚15〜20μm
試験片4:PC(ポリカーボネート)基材、膜厚15〜20μm
試験片の表面平滑性を目視評価した。評価は以下の基準で行った。
「◎」:平滑であり、虹や白化、クラック、ブツ等が無い。
「×」:虹や白化、クラック、ブツ等が確認される。
碁盤目剥離試験により、付着性を評価した。試験片に2mm間隔で10×10の碁盤目状にカッターナイフで切れ目を入れ、2mm2の碁盤目を100個作り、その上にセロハンテープを貼りつけて、急速に剥がす操作を行い、剥離せずに残存した碁盤目の数を数えた。評価は以下の基準で行った。
「4」:碁盤目の残存数が100個。
「3」:碁盤目の残存数が80〜99個。
「2」:碁盤目の残存数が50〜79個。
「1」:碁盤目の残存数が49個以下。
試験片を下記温度設定の熱風乾燥機に96時間放置した後の外観及び付着性を初期評価同様にして評価した。
BMC(バルクモールディングコンパウンド)基材(試験片1、2)・・・200℃
ABS(アクリロニトリル−ブタジエン−スチレン共重合樹脂)基材(試験片3)・・・80℃
PC(ポリカーボネート)基材(試験片4)・・・120℃
硬化性組成物を40℃で3ヶ月間保存し、貯蔵安定性を目視評価した。評価は以下の基準で行った。
「◎」:外観及び粘度変化なし。
「×」:粘度変化がある、又はゲル化物が生成している。
Claims (8)
- 分子構造中に不飽和結合を有し、油長が10〜80の範囲であるアルキド樹脂(A)と、分子構造中に不飽和結合を有する重合性モノマー(B)とを必須の構成成分とする共重合体であって、前記分子構造中に不飽和結合を有する重合性モノマー(B)が、(メタ)アクリレートモノマーと芳香族ビニルモノマーとを必須の成分とし、前記分子構造中に不飽和結合を有するアルキド樹脂(A)と、前記子構造中に不飽和結合を有する重合性モノマー(B)との質量比[(A)/(B)]が50/50〜90/10の範囲であることを特徴とするアクリル変性アルキド樹脂。
- 前記分子構造中に不飽和結合を有する重合性モノマー(B)が、水酸基含有(メタ)アクリレートモノマーを必須の成分とする請求項1記載のアクリル変性アルキド樹脂。
- 請求項1又は2に記載のアクリル変性アルキド樹脂と、(メタ)アクリレート化合物(X)とを必須の成分として含有する硬化性組成物。
- 請求項3記載の硬化性組成物の硬化物。
- 請求項3記載の硬化性組成物を用いてなる無機材料薄膜下塗り用コーティング剤。
- 無機材料薄膜の厚さが30nm〜3μmの範囲である請求項5記載の無機材料薄膜下塗り用コーティング剤。
- 無機材料薄膜が真空蒸着又はスパッタリングにて形成されたものである請求項5記載の無機材料薄膜下塗り用コーティング剤。
- 請求項5記載の無機材料薄膜下塗り用コーティング剤からなる下塗り層を有する成形体。
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PCT/JP2017/006771 WO2017154591A1 (ja) | 2016-03-10 | 2017-02-23 | アクリル変性アルキド樹脂及び無機材料薄膜下塗り用コーティング剤 |
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JPS5462294A (en) * | 1977-10-28 | 1979-05-19 | Dainippon Ink & Chem Inc | Preparation of modified copolymer |
JPS6123652A (ja) * | 1984-07-11 | 1986-02-01 | Dainippon Ink & Chem Inc | 塗料用樹脂の製造法 |
JPS6220566A (ja) * | 1985-07-19 | 1987-01-29 | Mitsubishi Petrochem Co Ltd | 被覆用樹脂組成物 |
JP2003026710A (ja) * | 2001-07-13 | 2003-01-29 | Nippon Synthetic Chem Ind Co Ltd:The | 紫外線硬化型樹脂組成物、塗膜形成方法及びその用途 |
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CN108779220A (zh) | 2018-11-09 |
JPWO2017154591A1 (ja) | 2018-03-22 |
US10781316B2 (en) | 2020-09-22 |
EP3428206A1 (en) | 2019-01-16 |
EP3428206B1 (en) | 2021-06-23 |
CN108779220B (zh) | 2021-03-30 |
US20190055411A1 (en) | 2019-02-21 |
TWI781092B (zh) | 2022-10-21 |
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WO2017154591A1 (ja) | 2017-09-14 |
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