JPH03128982A - Coating resin composition - Google Patents

Coating resin composition

Info

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
Application number
JP26618689A
Other languages
Japanese (ja)
Other versions
JP2825554B2 (en
Inventor
Hiroshi Kagono
楮野 博司
Taisaku Kano
加納 泰作
Tsukasa Murakami
司 村上
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mitsui Toatsu Chemicals Inc
Original Assignee
Mitsui Toatsu Chemicals Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Mitsui Toatsu Chemicals Inc filed Critical Mitsui Toatsu Chemicals Inc
Priority to JP26618689A priority Critical patent/JP2825554B2/en
Publication of JPH03128982A publication Critical patent/JPH03128982A/en
Application granted granted Critical
Publication of JP2825554B2 publication Critical patent/JP2825554B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Paints Or Removers (AREA)
  • Polyurethanes Or Polyureas (AREA)

Abstract

PURPOSE:To obtain the title composition excellent in the balance between the dryability and the appearance by using a specified acrylic polyol in a two-pack acrylic urethane coating resin composition consisting of a principal component composed mainly of an acrylic polyol and a curing agent comprising a polyisocyanate. CONSTITUTION:A two-pack acrylic urethane coating resin composition consisting of a principal component composed mainly of an acrylic polyol and a curing agent comprising a polyisocyanate which are mixed before use, wherein an acrylic polyol mixture containing a low molecular acrylic polyol (A) (e.g. a copolymer of methyl, n-butyl or hydroxyethyl methacrylate, hydroxyethyl acrylate, styrene, or methacrylic acid) having a number-average molecular weight of 7, 000 or lower and a high-molecular acrylic polyol (B) (e.g. a copolymer obtained from the same raw material as that for the copolymer mentioned above) having a number-average molecular weight of 10,000 or higher at a weight ratio of A to B of 00.5 to 9 is used as the acrylic polyol.

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.

〔従来の技術〕[Conventional technology]

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.

〔発明が解決しようとする課題〕[Problem to be solved by the invention]

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. .

〔課題を解決するための手段〕[Means to solve the problem]

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.

〔実施例〕〔Example〕

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)

【特許請求の範囲】 1、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.
JP26618689A 1989-10-16 1989-10-16 Resin composition for paint Expired - Fee Related JP2825554B2 (en)

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

Family Applications (1)

Application Number Title Priority Date Filing Date
JP26618689A Expired - Fee Related JP2825554B2 (en) 1989-10-16 1989-10-16 Resin composition for paint

Country Status (1)

Country Link
JP (1) JP2825554B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008003714A (en) * 2006-06-20 2008-01-10 Toshiba Corp Component coupling structure and electronic apparatus

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101947240B1 (en) * 2016-11-21 2019-02-12 주식회사 케이씨씨 Coating composition

Cited By (1)

* Cited by examiner, † Cited by third party
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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