JPH03128982A - Coating resin composition - Google Patents
Coating resin compositionInfo
- Publication number
- JPH03128982A JPH03128982A JP26618689A JP26618689A JPH03128982A JP H03128982 A JPH03128982 A JP H03128982A JP 26618689 A JP26618689 A JP 26618689A JP 26618689 A JP26618689 A JP 26618689A JP H03128982 A JPH03128982 A JP H03128982A
- Authority
- JP
- Japan
- Prior art keywords
- acrylic polyol
- acrylic
- molecular weight
- resin composition
- polyol
- 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.)
- Granted
Links
- 239000011342 resin composition Substances 0.000 title claims abstract description 13
- 239000011248 coating agent Substances 0.000 title abstract description 11
- 238000000576 coating method Methods 0.000 title abstract description 11
- 229920005862 polyol Polymers 0.000 claims abstract description 42
- -1 acrylic polyol Chemical class 0.000 claims abstract description 41
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims abstract description 22
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims abstract description 16
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 10
- 239000005056 polyisocyanate Substances 0.000 claims abstract description 10
- 229920001228 polyisocyanate Polymers 0.000 claims abstract description 10
- 239000003973 paint Substances 0.000 claims description 27
- 238000002156 mixing Methods 0.000 claims description 9
- 239000000203 mixture Substances 0.000 abstract description 5
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 abstract description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract description 4
- 229920001577 copolymer Polymers 0.000 abstract description 4
- 239000002994 raw material Substances 0.000 abstract description 3
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 abstract description 2
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 abstract description 2
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 abstract description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 229920005903 polyol mixture Polymers 0.000 abstract 1
- 238000001035 drying Methods 0.000 description 15
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 239000000178 monomer Substances 0.000 description 8
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 5
- 230000007423 decrease Effects 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 239000000049 pigment Substances 0.000 description 4
- 150000003077 polyols Chemical class 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 229920002554 vinyl polymer Polymers 0.000 description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 125000005442 diisocyanate group Chemical group 0.000 description 3
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- 239000008096 xylene Substances 0.000 description 3
- ALQLPWJFHRMHIU-UHFFFAOYSA-N 1,4-diisocyanatobenzene Chemical compound O=C=NC1=CC=C(N=C=O)C=C1 ALQLPWJFHRMHIU-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 2
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 2
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 2
- 239000002075 main ingredient Substances 0.000 description 2
- AYLRODJJLADBOB-QMMMGPOBSA-N methyl (2s)-2,6-diisocyanatohexanoate Chemical compound COC(=O)[C@@H](N=C=O)CCCCN=C=O AYLRODJJLADBOB-QMMMGPOBSA-N 0.000 description 2
- 238000010926 purge Methods 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- QXRRAZIZHCWBQY-UHFFFAOYSA-N 1,1-bis(isocyanatomethyl)cyclohexane Chemical compound O=C=NCC1(CN=C=O)CCCCC1 QXRRAZIZHCWBQY-UHFFFAOYSA-N 0.000 description 1
- ZXHZWRZAWJVPIC-UHFFFAOYSA-N 1,2-diisocyanatonaphthalene Chemical compound C1=CC=CC2=C(N=C=O)C(N=C=O)=CC=C21 ZXHZWRZAWJVPIC-UHFFFAOYSA-N 0.000 description 1
- CDMDQYCEEKCBGR-UHFFFAOYSA-N 1,4-diisocyanatocyclohexane Chemical compound O=C=NC1CCC(N=C=O)CC1 CDMDQYCEEKCBGR-UHFFFAOYSA-N 0.000 description 1
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 1
- QZPSOSOOLFHYRR-UHFFFAOYSA-N 3-hydroxypropyl prop-2-enoate Chemical compound OCCCOC(=O)C=C QZPSOSOOLFHYRR-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920000298 Cellophane Polymers 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- WMTLVUCMBWBYSO-UHFFFAOYSA-N N=C=O.N=C=O.C=1C=CC=CC=1OC1=CC=CC=C1 Chemical compound N=C=O.N=C=O.C=1C=CC=CC=1OC1=CC=CC=C1 WMTLVUCMBWBYSO-UHFFFAOYSA-N 0.000 description 1
- QORUGOXNWQUALA-UHFFFAOYSA-N N=C=O.N=C=O.N=C=O.C1=CC=C(C(C2=CC=CC=C2)C2=CC=CC=C2)C=C1 Chemical compound N=C=O.N=C=O.N=C=O.C1=CC=C(C(C2=CC=CC=C2)C2=CC=CC=C2)C=C1 QORUGOXNWQUALA-UHFFFAOYSA-N 0.000 description 1
- 229920000265 Polyparaphenylene Polymers 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- KXBFLNPZHXDQLV-UHFFFAOYSA-N [cyclohexyl(diisocyanato)methyl]cyclohexane Chemical compound C1CCCCC1C(N=C=O)(N=C=O)C1CCCCC1 KXBFLNPZHXDQLV-UHFFFAOYSA-N 0.000 description 1
- BWLKKFSDKDJGDZ-UHFFFAOYSA-N [isocyanato(phenyl)methyl]benzene Chemical compound C=1C=CC=CC=1C(N=C=O)C1=CC=CC=C1 BWLKKFSDKDJGDZ-UHFFFAOYSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 230000008094 contradictory effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003759 ester based solvent Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-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
- 239000005453 ketone based solvent Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- DGTNSSLYPYDJGL-UHFFFAOYSA-N phenyl isocyanate Chemical compound O=C=NC1=CC=CC=C1 DGTNSSLYPYDJGL-UHFFFAOYSA-N 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- AFCAKJKUYFLYFK-UHFFFAOYSA-N tetrabutyltin Chemical compound CCCC[Sn](CCCC)(CCCC)CCCC AFCAKJKUYFLYFK-UHFFFAOYSA-N 0.000 description 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 1
- 150000003606 tin compounds Chemical class 0.000 description 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Paints Or Removers (AREA)
- Polyurethanes Or Polyureas (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、乾燥性と外観のバランスがとれた、2液型ア
クリルウレタン塗料用樹脂組成物に関する。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a resin composition for a two-component acrylic urethane paint that has a good balance between drying properties and appearance.
2液型アクリルウレタン塗料において、乾燥性の向上は
アクリルポリオールを主成分とする主剤に硝化綿やセル
ロースアセテートブチレート(CAB)など、硬い樹脂
をブレンドするか、ポリオールの分子量を大きくすれば
実現できる。In two-component acrylic urethane paints, drying performance can be improved by blending a hard resin such as nitrified cotton or cellulose acetate butyrate (CAB) with the acrylic polyol as the main ingredient, or by increasing the molecular weight of the polyol. .
しかし塗料の粘度が高くなり、塗膜のフロー性が低下す
るため外観は低下すし、作業性上も劣る。However, the viscosity of the paint increases and the flowability of the paint film decreases, resulting in poor appearance and poor workability.
また、硝化綿やCAB等は、アクリルポリオールの組成
物に制限があった。Furthermore, nitrified cotton, CAB, and the like have limitations in the composition of acrylic polyols.
外観のよい塗料を得るには、−船釣には低分子量のアク
リルポリオールの様な塗膜のフロー性良好なハイソリッ
ド型が適用可能である。In order to obtain a paint with a good appearance, - For boat fishing, it is possible to use a high solid type paint film with good flowability, such as a low molecular weight acrylic polyol.
しかし、アクリルポリオールが低分子量となると、乾燥
性は低下し、耐湿気性、耐薬品性、耐候性等の性能を低
下させる傾向にあった。However, when the molecular weight of the acrylic polyol becomes low, the drying properties tend to decrease and performance such as moisture resistance, chemical resistance, and weather resistance tends to decrease.
また、低分子量のため、塗料時、塗料がたれ易い欠点を
有していた。Furthermore, due to its low molecular weight, it had the disadvantage that the paint easily dripped when applied.
このように、乾燥性を上げれば外観が低下し、また外観
を上げれば、乾燥性が低下するという相反する傾向にあ
り、乾燥性、外観のバランスのれた塗料用樹脂組成物が
望まれた。As described above, there is a contradictory tendency that increasing the drying property reduces the appearance, and increasing the appearance reduces the drying property.Therefore, there was a desire for a resin composition for paints with a balance between drying property and appearance. .
本発明は、上記の問題点を解決するため、鋭意検討した
結果、2液型アクリルウレタン塗料において、主成分で
あるアクリルポリオールの低分子量アクリルポリオール
に高分子量アクリルポリオールを混治することにより、
乾燥性と外観のバランスがとれた2液型アクリルウレタ
ン塗料用樹脂組成物を開発でき、漸く本発明を完成した
。In order to solve the above problems, the present invention was developed as a result of intensive studies, and by co-curing a high molecular weight acrylic polyol with a low molecular weight acrylic polyol of the acrylic polyol that is the main component in a two-component acrylic urethane paint,
We were able to develop a two-component acrylic urethane paint resin composition that has a good balance between drying properties and appearance, and finally completed the present invention.
即ち、本発明は、アクリルポリオールを主成分とする主
剤と、ポリイソシアネートである硬化剤とを使用時に混
合して用いる2液型アクリルウレタン塗料用樹脂組底物
において、該アクリルポリオールが、
(1)数平均分子量が7,000以下の低分子量アクリ
ルポリオール(A)と
(2)数平均分子量が10,000以上のアクリル高分
子量ポリオール(B)を含有し、
(3)AとBの混合比率が、重量比で
0.5≦(A)/ (B)≦9の範囲にある2液型アク
リルウレタン塗料用樹脂組成物を提供することを目的と
する。That is, the present invention provides a resin composition for a two-component acrylic urethane paint in which a main component mainly composed of an acrylic polyol and a curing agent which is a polyisocyanate are mixed at the time of use, wherein the acrylic polyol is (1) ) contains a low molecular weight acrylic polyol (A) with a number average molecular weight of 7,000 or less and (2) an acrylic high molecular weight polyol (B) with a number average molecular weight of 10,000 or more; (3) a mixing ratio of A and B; An object of the present invention is to provide a resin composition for a two-component acrylic urethane paint in which the weight ratio is in the range of 0.5≦(A)/(B)≦9.
本発明に使用する低分子量アクリルポリオール(A)と
しては、数平均分子量が7.000以下、好ましくは4
,000〜7,000が適当である。The low molecular weight acrylic polyol (A) used in the present invention has a number average molecular weight of 7.000 or less, preferably 4.
,000 to 7,000 is appropriate.
低分子量アクリルポリオールの数平均分子量が4.00
0以下では、十分な乾燥性が得られなく、7.000を
越えると外観が低下する傾向にある。The number average molecular weight of the low molecular weight acrylic polyol is 4.00.
If it is less than 0, sufficient drying properties cannot be obtained, and if it exceeds 7.000, the appearance tends to deteriorate.
また、高分子量アクリルポリオール(B)としては、数
平均分子量が10,000以上、好ましくは、12.0
00〜20,000が適当である。Further, the high molecular weight acrylic polyol (B) has a number average molecular weight of 10,000 or more, preferably 12.0
00 to 20,000 is appropriate.
高分子量アクリルポリオールの数平均分子量が12.0
00未満では、十分な乾燥性が得られなく、20.00
0を越えると外観が低下し好ましくない。The number average molecular weight of high molecular weight acrylic polyol is 12.0
If it is less than 20.00, sufficient drying properties cannot be obtained;
If it exceeds 0, the appearance deteriorates, which is not preferable.
低分子量アクリルポリオール(A)と高分子量アクリル
ポリオール(B)の混合比率は重量比で、0.5≦(A
)/ (B)≦9の範囲が適当である。The mixing ratio of low molecular weight acrylic polyol (A) and high molecular weight acrylic polyol (B) is 0.5≦(A
)/(B)≦9 is appropriate.
(A)/ (B)が9を越えると、乾燥性が極端に遅く
なり、0.5未満では外観が低下する。When (A)/(B) exceeds 9, the drying property becomes extremely slow, and when it is less than 0.5, the appearance deteriorates.
本発明で用いられるアクリルポリオールとしては、−i
にラジカル重合による溶液混合で合成された共重合体が
適当であり、例えば水酸基含有ビニルモノマーとアクリ
ル系モノマーとの共重合せしめて得られる。The acrylic polyol used in the present invention includes -i
A copolymer synthesized by solution mixing using radical polymerization is suitable, and can be obtained, for example, by copolymerizing a hydroxyl group-containing vinyl monomer and an acrylic monomer.
ここで水酸基含有モノマーとしては、例えばアクリル酸
もしくはメタクリル酸と、炭素数2〜IOのグリコール
とのモノエステルが挙げられ、具体的には、ヒドロキシ
エチルアクリレート、ヒドロキシエチルメタクリレート
、ヒドロキシプロピルアクリレート、ヒドロキシプロピ
ルメタクリレート等を例示できる。Here, the hydroxyl group-containing monomer includes, for example, a monoester of acrylic acid or methacrylic acid and a glycol having 2 to 10 carbon atoms, and specifically, hydroxyethyl acrylate, hydroxyethyl methacrylate, hydroxypropyl acrylate, hydroxypropyl Examples include methacrylate.
アクリル系モノマーとしては、例えば、アクリル酸もし
くはメタクリル酸のアルキル(炭素数1〜24)エステ
ル等が挙げられ、更にアクリル酸、メタクリル酸の如き
カルボキシ基含有ビニルモノマー、アマイド系ビニルモ
ノマー、グリシジル基m有ビニルモノマー、スチレン及
びその誘導体、アクリロニトリル、ビニルトルエン、塩
化ビニル、酢酸ビニル等も併用できる。これらは単独又
は2種以上混合して使用される。Examples of acrylic monomers include alkyl (carbon numbers 1 to 24) esters of acrylic acid or methacrylic acid, and also carboxy group-containing vinyl monomers such as acrylic acid and methacrylic acid, amide vinyl monomers, and glycidyl group m Vinyl monomers, styrene and its derivatives, acrylonitrile, vinyltoluene, vinyl chloride, vinyl acetate, etc. can also be used in combination. These may be used alone or in combination of two or more.
本発明において、上記アクリルポリオール単独が好まし
いが、ポリエステルポリオール、エポキシポリオール等
地の成分も併用できる。In the present invention, the above acrylic polyol alone is preferred, but other components such as polyester polyol and epoxy polyol can also be used in combination.
本発明で用いるアクリルポリオールとしては、水酸基が
10〜150KOI(■/g程度のものを使用するのが
好ましく、水酸基が10 KOH■/gであると耐水性
等が低下し、150KOH■/gをこえると密着性が低
下する。As the acrylic polyol used in the present invention, it is preferable to use one with a hydroxyl group of 10 to 150 KOI (■/g). If the hydroxyl group is 10 KOH■/g, water resistance etc. will decrease, and 150 KOH■/g If it exceeds the limit, the adhesion will decrease.
より好ましいアクリルポリオールとしては、水酸基が3
0〜80KOI(■/g程度のものである。A more preferable acrylic polyol has 3 hydroxyl groups.
It is about 0 to 80 KOI (■/g).
本発明に使用される硬化剤としてのポリイソシアネート
としては、通常用いられる公知のポリイソシアネートな
ら何れも使用できる。As the polyisocyanate used as a curing agent in the present invention, any commonly used and known polyisocyanate can be used.
これ等ポリイソシアネートとしては、例えば、ヘキサメ
チレンジイソシアネート(HMDI) 、リジンジイソ
シアネート(LDI) 、イソホロンジイソシアネート
(IPDI)、1,4−シクロヘキサンジイソシアネー
ト、ジシクロヘキシルメタンジイソシアネート(HMD
I)、ビス(イソシアナトメチル)シクロヘキサン(H
XDT)等の、脂肪族又は脂環族ジイソシアネート、或
いは、トリレンジイソシアネート(TDI) 、ジフェ
ニルメタンイソシアネート(MDI)、p−フェニレン
ジイソシアネート(PPDI)、キシレンジイソシアネ
ート(XDI) 、ジフェニルエーテルジイソシアネー
ト、トリジンジイソシアネート、ジアニシジンジイソシ
アネート、ナフタレンジイソシアネート(MDI)等芳
香族ジイソシアネート、又はクルードトリレンジイソシ
アネート(クルード↑DI)、ポリメチレンポリフェニ
レンポリイソシアネート(ポリメリックMDI)、トリ
フヱニルメタントリイソシアネート、トリス(フェニル
イソシアネート)チオフォスフェート等の芳香族ポリイ
ソシアネート、及び上記のジイソシアネートモノマーの
イソシアヌレート変性体、ビューレット変性体体、カル
ボジイミド変性体等のイソシアネート変性体が使用でき
る。Examples of these polyisocyanates include hexamethylene diisocyanate (HMDI), lysine diisocyanate (LDI), isophorone diisocyanate (IPDI), 1,4-cyclohexane diisocyanate, and dicyclohexylmethane diisocyanate (HMD).
I), bis(isocyanatomethyl)cyclohexane (H
Aliphatic or alicyclic diisocyanates such as XDT), or tolylene diisocyanate (TDI), diphenylmethane isocyanate (MDI), p-phenylene diisocyanate (PPDI), xylene diisocyanate (XDI), diphenyl ether diisocyanate, tolidine diisocyanate, dianisidine Aromatic diisocyanates such as diisocyanate and naphthalene diisocyanate (MDI), or aromatic substances such as crude tolylene diisocyanate (crude↑DI), polymethylene polyphenylene polyisocyanate (polymeric MDI), triphenylmethane triisocyanate, and tris(phenylisocyanate) thiophosphate. Group polyisocyanates, and isocyanate-modified products such as isocyanurate-modified products, biuret-modified products, and carbodiimide-modified products of the above-mentioned diisocyanate monomers can be used.
ポリオールとポリイソシアネートの配合比は、目的によ
り種々選択できるが、本発明ではイソシアネート基(N
CO)と水酸基(OH)との当量比(NCO10H)が
0.7〜1.5の範囲となるように構成するのが好まし
い。The blending ratio of polyol and polyisocyanate can be variously selected depending on the purpose, but in the present invention, isocyanate groups (N
It is preferable that the equivalent ratio (NCO10H) of CO) and hydroxyl group (OH) be in the range of 0.7 to 1.5.
本発明の組成物には、更に錫化合物等の触媒を配合する
のが好ましい。It is preferable that the composition of the present invention further contains a catalyst such as a tin compound.
上記の触媒としては、ウレタン化反応に通常用いられる
ものが使用できるが、錫系化合物が最も好ましい。As the above catalyst, those commonly used in urethanization reactions can be used, but tin-based compounds are most preferred.
これらの化合物としては、例えば、ジブチル錫ラウレー
ト、ジプチル錫ジ(2−エチルヘキソエート〉、塩化錫
、テトラ −n−ブチル錫等が挙げられる。この中でも
、ジブチル錫ラウレートが特に好ましい。Examples of these compounds include dibutyltin laurate, diptyltin di(2-ethylhexoate), tin chloride, and tetra-n-butyltin. Among these, dibutyltin laurate is particularly preferred.
上記触媒の配合量は、アクリルポリオール100重量部
当り、0.O1〜0.5重量部程度が適している。The blending amount of the above catalyst is 0.00 parts per 100 parts by weight of the acrylic polyol. Approximately 1 to 0.5 parts by weight of O is suitable.
本発明では、更に、この種の塗料組成物に通常配合され
ている着色顔料、体質顔料、アルミフレーク等の顔料や
レヘリング剤、沈降防止剤等を必要により配合すること
もできる。In the present invention, pigments such as coloring pigments, extender pigments, aluminum flakes, etc., leveling agents, anti-settling agents, etc., which are usually blended in this type of coating composition, can also be blended as necessary.
又、有機溶剤としては、例えばトルエン、キシレン等の
芳香族炭化水素系溶剤、メチルエチルケトン、メチルイ
ソブチルケトン等のケトン系溶剤、酢酸エチル、セロソ
ルブアセテート等のエステル系溶剤が使用できる。Further, as the organic solvent, for example, aromatic hydrocarbon solvents such as toluene and xylene, ketone solvents such as methyl ethyl ketone and methyl isobutyl ketone, and ester solvents such as ethyl acetate and cellosolve acetate can be used.
本発明の2液型アクリルウレタン塗料用樹脂組成物を使
用するに当っては、例えば、塗装粘度(フォードカップ
#420°C)が10〜20秒、好ましくは13〜17
秒になるように調整し、エアスプレ、エアレススプレー
等の従来公知の塗装方法に従い、硬化塗膜が10〜40
μ程度になるように塗装するのがよい。When using the two-component acrylic urethane paint resin composition of the present invention, for example, the coating viscosity (Ford cup #420°C) is 10 to 20 seconds, preferably 13 to 17 seconds.
The cured coating film is adjusted to 10 to 40 seconds and then applied according to conventionally known painting methods such as air spray or airless spray.
It is best to paint so that the thickness is around μ.
また、ペーパキュアー、ペーパーインジェクションキュ
アー(V I C)等の塗装後、あるいは塗装時に、三
級アミン蒸気と接触させる塗装システムにも適応できる
。It can also be applied to coating systems such as paper cure, paper injection cure (VIC), etc., in which the coating system is brought into contact with tertiary amine vapor after or during coating.
本発明によれば、従来の様に、アクリルポリオールを主
成分とする主剤に、硝化綿やセルロースアセテートブチ
レート(CAB)など、硬い樹脂をブレンドする必要が
ないので、塗料の粘度が比較的低くなり、塗膜のフロー
性が向上するため外観は極めて優れ、且つ、乾燥性の優
れたウレタン2液型アクリルウレタン系塗料用樹脂組戒
物を提供できる。According to the present invention, there is no need to blend a hard resin such as nitrified cotton or cellulose acetate butyrate (CAB) into a base agent mainly composed of acrylic polyol, as in the past, so the viscosity of the paint is relatively low. Therefore, it is possible to provide a resin composition for a two-component urethane type acrylic urethane paint, which has an extremely excellent appearance due to improved flowability of the coating film, and has excellent drying properties.
以下、本発明を更に具体的に説明するため、実施例及び
比較例をあげて説明するが、本発明はこれらの実施例に
限定されるものではない。EXAMPLES Hereinafter, in order to explain the present invention more specifically, Examples and Comparative Examples will be given and explained, but the present invention is not limited to these Examples.
参考例1
アク1ルボIオール a の
攪拌機、温度計、還流コンデンサー及び窒素導入管を備
えた4つロフラスコに、窒素をパージした後、フラスコ
にキジロール100部を仕込み130°Cに加熱昇温し
た。次に表−1に示す原料を5.5時間に渡り滴下して
、1.5時間後には110℃にて2時間保持して、固形
公約50%のアクリルポリオールを得た。Reference Example 1 After purging nitrogen into a four-bottle flask equipped with a stirrer, a thermometer, a reflux condenser, and a nitrogen introduction tube, 100 parts of Kijirole was charged into the flask and the temperature was raised to 130°C. . Next, the raw materials shown in Table 1 were added dropwise over 5.5 hours, and after 1.5 hours, the mixture was held at 110°C for 2 hours to obtain an acrylic polyol with a solid content of about 50%.
参考例2
アク1ルポリオール b の
0
攪拌機、温度計、還流コンデンサー及び窒素導入管を備
えた4つロフラスコに、窒素をパージした後、フラスコ
にキジロール70部を仕込み100°Cに加熱昇温した
。次に表−1に示す原料を5.5時間に渡り滴下して、
滴下後回し温度でさらに5時間保持した後、キジロール
を30部加え、固形公約50%のアクリルポリオールを
得た。Reference Example 2 Acrylic Polyol b No. 0 After purging nitrogen into a four-bottle flask equipped with a stirrer, thermometer, reflux condenser, and nitrogen inlet tube, 70 parts of Kijirole was charged into the flask and the temperature was raised to 100°C. . Next, the raw materials shown in Table 1 were added dropwise over 5.5 hours.
After the dropwise addition and holding at the temperature for an additional 5 hours, 30 parts of Kijirole was added to obtain an acrylic polyol with a solid content of approximately 50%.
実施例1〜4 ペースコー Sの1堅 ベースコート塗料を下記の様に配合した。Examples 1-4 Pacco S 1st Ken The base coat paint was formulated as follows.
合成したアクリル樹脂(固形分50χ)70部酸化チタ
ンCR−90(石原産業社製) 46.5部シンナ
(キシレン:トルエン:酢酸ブチル:
メチルイソブチルケトン−2:1:1:1) 30部
レジごツクスRL−4(レベリンク剤;三井東圧圧化学
社製)0.07部
VIC5054(アッシュランドケごカル社製)0.0
7部
上記配合にて、ペイントシェーカーにより1時1
間顔料を分散した。Synthesized acrylic resin (solid content 50χ) 70 parts Titanium oxide CR-90 (manufactured by Ishihara Sangyo Co., Ltd.) 46.5 parts Thinner (xylene: toluene: butyl acetate: methyl isobutyl ketone -2:1:1:1) 30 parts Cash register Gotsukusu RL-4 (level linking agent; manufactured by Mitsui Toatsu Chemical Co., Ltd.) 0.07 parts VIC5054 (manufactured by Ashland Kegokal Co., Ltd.) 0.0
7 parts The pigment was dispersed in the above formulation for 1 hour using a paint shaker.
硬化剤は、オレスターNP100O(三井東圧化学社製
)を、当量比がNC0101−I−1になるよう配合し
、さらに上記シンナーにて希釈し、フォードカップ#4
にて14秒/20°Cに粘度調整し、ヘースコート塗料
を得た。As a curing agent, Olestar NP100O (manufactured by Mitsui Toatsu Chemical Co., Ltd.) was blended so that the equivalent ratio was NC0101-I-1, and further diluted with the above thinner.
The viscosity was adjusted to 14 seconds/20°C to obtain a hair coat paint.
アクリルポリオール樹脂の配合例を表−2に示す。Table 2 shows blending examples of acrylic polyol resins.
この塗料を、5PCC−5[l#144処理板に、VI
Cシステムにて、膜厚30μmになるようにスプレーし
た。Apply this paint to the 5PCC-5 [l #144 treated plate, VI
It was sprayed using a C system to a film thickness of 30 μm.
結果を表−3に示す。The results are shown in Table-3.
比較例1〜4 実施例と全く同し様にしてヘースコート塗料を得た。Comparative examples 1 to 4 A hair coat paint was obtained in exactly the same manner as in the example.
アクリルポリオール樹脂の配合例を表−2に示す。Table 2 shows blending examples of acrylic polyol resins.
この塗料を、実施例と同様に、5PCC−3B#144
処理板に、VTGシステムにて、膜厚30μmになるよ
うにスプレーした。This paint was applied to 5PCC-3B#144 as in the example.
The treated plate was sprayed with a VTG system to a film thickness of 30 μm.
2 結果を表 3に示す。2 Display results Shown in 3.
性能評価は次のようにして行なった。Performance evaluation was performed as follows.
1)目視外観 塗膜外観の秀れているものを◎、劣るもの×とした。1) Visual appearance Those with excellent coating film appearance were rated ◎, and those with poor coating film appearance were rated ×.
2)光沢 光沢は60°Cグロスでの光沢計の数値を測定した。2) Gloss The gloss was measured using a gloss meter at 60°C gloss.
3)乾燥性
指触乾燥時間と、完全硬化時間(指でおして跡が残らな
い)
4)密着性
JIS K5400
のゴバン目セロハンテープ試験
3
表
5
16
〔発明の効果〕
本発明による2液型アクリルウレタン塗料用樹脂組底物
は、バランスがとれ、乾燥性及び外観が優れているのに
比べ、従来の高分子アクリルポリオールンを主剤とする
2液型アクリルウレタン塗料用樹脂組底物(比較例4)
は乾燥性の速いが外観の低下を招き、低分子アクリルポ
リオールンを主剤とする2液型アクリルウレタン塗料用
樹脂組成物(比較例3)は外観に優れるが乾燥性に劣る
ことは表3から明らかである。3) Drying time to the touch and complete curing time (no marks left when rubbed with fingers) 4) Adhesion JIS K5400 cellophane tape test 3 Table 5 16 [Effects of the invention] Two-component acrylic according to the present invention Resin bottoms for urethane paints are well-balanced and have excellent drying properties and appearance, whereas conventional resin bottoms for two-component acrylic urethane paints (comparative example 4)
Table 3 shows that although drying property is fast, the appearance deteriorates, and the two-component acrylic urethane paint resin composition (Comparative Example 3), which has low molecular weight acrylic polyol as the main ingredient, has excellent appearance but poor drying property. it is obvious.
Claims (1)
ソシアネートである硬化剤とを、使用時に混合して用い
る2液型アクリルウレタン塗料用樹脂組成物において、
該アクリルポリオールが、 (1)数平均分子量が7,000以下の低分子量アクリ
ルポリオール(A)と (2)数平均分子量が10,000以上の高分子量アク
リルポリオール(B)を含有し、(3)AとBの混合比
率が、重量比で 0.5≦(A)/(B)≦9の範囲にあることを特徴と
する2液型アクリルウレタン塗料用樹脂組成物。[Scope of Claims] 1. A two-component acrylic urethane paint resin composition in which a main component containing an acrylic polyol and a curing agent which is a polyisocyanate are mixed at the time of use,
The acrylic polyol contains (1) a low molecular weight acrylic polyol (A) having a number average molecular weight of 7,000 or less and (2) a high molecular weight acrylic polyol (B) having a number average molecular weight of 10,000 or more; ) A resin composition for a two-component acrylic urethane paint, characterized in that the mixing ratio of A and B is in the range of 0.5≦(A)/(B)≦9 in terms of weight ratio.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP26618689A JP2825554B2 (en) | 1989-10-16 | 1989-10-16 | Resin composition for paint |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP26618689A JP2825554B2 (en) | 1989-10-16 | 1989-10-16 | Resin composition for paint |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH03128982A true JPH03128982A (en) | 1991-05-31 |
JP2825554B2 JP2825554B2 (en) | 1998-11-18 |
Family
ID=17427453
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JP26618689A Expired - Fee Related JP2825554B2 (en) | 1989-10-16 | 1989-10-16 | Resin composition for paint |
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JP (1) | JP2825554B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008003714A (en) * | 2006-06-20 | 2008-01-10 | Toshiba Corp | Component coupling structure and electronic apparatus |
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KR101947240B1 (en) * | 2016-11-21 | 2019-02-12 | 주식회사 케이씨씨 | Coating composition |
-
1989
- 1989-10-16 JP JP26618689A patent/JP2825554B2/en not_active Expired - Fee Related
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008003714A (en) * | 2006-06-20 | 2008-01-10 | Toshiba Corp | Component coupling structure and electronic apparatus |
Also Published As
Publication number | Publication date |
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JP2825554B2 (en) | 1998-11-18 |
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