JPS6028459A - Acrylic lacquer - Google Patents

Acrylic lacquer

Info

Publication number
JPS6028459A
JPS6028459A JP13510783A JP13510783A JPS6028459A JP S6028459 A JPS6028459 A JP S6028459A JP 13510783 A JP13510783 A JP 13510783A JP 13510783 A JP13510783 A JP 13510783A JP S6028459 A JPS6028459 A JP S6028459A
Authority
JP
Japan
Prior art keywords
copolymer
lacquer
weight
acrylic lacquer
acrylic
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.)
Pending
Application number
JP13510783A
Other languages
Japanese (ja)
Inventor
Keiji Sakata
坂田 慶治
Toashi Kishi
岸 東亜士
Kenji Uchiyama
健治 内山
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 JP13510783A priority Critical patent/JPS6028459A/en
Publication of JPS6028459A publication Critical patent/JPS6028459A/en
Pending legal-status Critical Current

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  • Paints Or Removers (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

PURPOSE:To provide an acrylic lacquer for application to iron plate, etc., with high water, weather and chemical resistance and coatability, which comprises a copolymer from p-methylstyrene and another monomer in a specific proportion. CONSTITUTION:The objective lacquer can be obtained by incorporating (A) a copolymer of a number-average molecular weight 5,000-50,000 from (i) 5- 95wt% of p-methylstyrene and (ii) 95-5wt% of another monomer (e.g., C1-18 alkyl acrylate or alkyl methacrylate) with, if required, (B) one or more ingredients selected from pigments, coating additives and fibrous compounds.

Description

【発明の詳細な説明】 本発明はアクリルラッカーに関し、更に詳しくは、特定
量のパラメチルスチレンを用いて得られる特定の共重合
体を用いることから成る耐水性、耐候性および耐薬品性
にすぐれたラッカーに関する。繊維素系化合物を含むラ
ッカー型塗料は、乾燥性などの性能面に加えて使用面で
の簡便さから、その用途も多方面にわたっている。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an acrylic lacquer, and more particularly to an acrylic lacquer having excellent water resistance, weather resistance and chemical resistance, which is obtained by using a specific copolymer obtained using a specific amount of para-methylstyrene. Regarding lacquer. Lacquer-type paints containing cellulose compounds are used in a wide variety of fields because of their performance, such as drying properties, and their ease of use.

これらのアクリルラッカーのうち樹脂組成として、スチ
レン、ビニールトルエン等の芳香族ビニールモノマーを
ハードモノマーとしたアクリルラッカーは、光沢、物性
の点で非常に優れており、特に多く使用されている。
Among these acrylic lacquers, acrylic lacquers whose resin composition includes aromatic vinyl monomers such as styrene and vinyltoluene as hard monomers are extremely excellent in terms of gloss and physical properties, and are particularly widely used.

しかし乍も、これらのアクリルラッカーを使用した塗料
は、常乾型の故に、架橋型塗料に比較して性能面、特に
耐水性、耐候性、耐薬品性等が劣り、これらの性質の改
善が望まれていた。
However, since paints using these acrylic lacquers are air-drying, they are inferior to cross-linked paints in terms of performance, especially water resistance, weather resistance, and chemical resistance, and it is difficult to improve these properties. It was wanted.

本発明者らは、上記の問題を解決するため鋭意検討した
結果、パラメチルスチレンを重合体の一成分とすること
により、これらの問題を一挙に解決できる事を見い出し
本発明に到達した。
As a result of intensive studies to solve the above problems, the present inventors discovered that these problems could be solved all at once by using paramethylstyrene as a component of the polymer, and arrived at the present invention.

即ち、本発明は、(A)ハラメチルスチレン5〜95重
量%と(B)他の共重合可能な単量体5−95重量%と
を共重合して得られる数平均分子量50.000である
共重合体および必要に応じて顔料、塗料用添加剤および
繊維系化合物の1種または2種以上を併用することを特
徴とするアクリルラッカーである。
That is, the present invention has a number average molecular weight of 50.000 obtained by copolymerizing (A) 5 to 95% by weight of halamethylstyrene and (B) 5 to 95% by weight of another copolymerizable monomer. This is an acrylic lacquer characterized by using a certain copolymer and, if necessary, one or more of pigments, paint additives, and fiber-based compounds.

ここにおいて、パラメチルスチレン(A)と共重合可能
な単量体(B)としては、例えば、炭素数1〜18を有
すアルキルアクリレート又はアルキルメタアクリレート
、β−ヒドロキシエチル(メタ)アクリレート、β−ヒ
ドロキシプロピル(メタ)アクリレート、アクリル酸、
メタアクリル酸、イタコン酸、フマル酸、無水マレイン
酸、グリシジル(メタ)アクリレート、2−エトキシメ
チル(メタ)アクリレート、2・エトキシメチル(メタ
)アクリレート、アクリロニトリル、メタアクリロニト
リル、シクロヘキシル(メタ)アクリレートなどが挙げ
られるが、これらは単独でまたは2種以上の混合物とし
て用いることが出来る。
Here, as the monomer (B) copolymerizable with paramethylstyrene (A), for example, alkyl acrylate or alkyl methacrylate having 1 to 18 carbon atoms, β-hydroxyethyl (meth)acrylate, β -Hydroxypropyl (meth)acrylate, acrylic acid,
Methacrylic acid, itaconic acid, fumaric acid, maleic anhydride, glycidyl (meth)acrylate, 2-ethoxymethyl (meth)acrylate, 2-ethoxymethyl (meth)acrylate, acrylonitrile, methacrylonitrile, cyclohexyl (meth)acrylate, etc. However, these can be used alone or in a mixture of two or more.

本発明に於いて、パラメチルスチレン(A)の使用量は
、得られる共重合物中に5〜95重量%、好ましくは1
0〜80重量%の範囲であり、他方、前記した共重合単
量体(B)の使用量は、5〜95重量%、好ましくは2
0〜90重量%の範囲である。
In the present invention, the amount of paramethylstyrene (A) used is 5 to 95% by weight, preferably 1% by weight in the resulting copolymer.
On the other hand, the amount of copolymerizable monomer (B) used is in the range of 5 to 95% by weight, preferably 2% by weight.
It ranges from 0 to 90% by weight.

本発明に於いてパラメチルスチレンの使用量が5重量%
より少い場合は、アクリルラッカーの耐水性および耐薬
品性(耐アルコール性)が劣り、逆に95重量%を超え
る場合は、耐候性が劣る。
In the present invention, the amount of paramethylstyrene used is 5% by weight.
If the amount is less, the water resistance and chemical resistance (alcohol resistance) of the acrylic lacquer will be poor, and if it exceeds 95% by weight, the weather resistance will be poor.

かかる単量体組成を有すアクリルラッカーは、ガラス転
移点が40〜95℃なる範囲(ガラス転移温度は、Fo
xの式により各単量体の単独重合体の転移温度より計算
された値を言う)にあることが、性能の面より好ましく
、パラメチルスチレンと共重合する各単量体の選択も、
このような観点からなされるべきでもある。又、当該共
重合体は、その数平均分子量が5,000〜50.00
0 の範囲にある事が必要であり、6,000〜3t1
.000の範囲であることが好ましい。而してこの場合
の数平均分子量は、常法に従ってゲルバーメーションク
ロマトグラフによるポリスチレン換算の値によって表わ
される。数平均分子量が5.0Onより低い場合は、耐
水性、耐薬品性および耐候性の点で十分でなく、逆に5
0.000よりも高分子量のものでは、スプレー作業性
の点で糸引き現象が起り問題がある。
The acrylic lacquer having such a monomer composition has a glass transition temperature in the range of 40 to 95°C (the glass transition temperature is Fo
From the viewpoint of performance, it is preferable that each monomer to be copolymerized with para-methylstyrene be selected as follows:
It should also be done from this perspective. Further, the copolymer has a number average molecular weight of 5,000 to 50.00.
It needs to be in the range of 0, 6,000 to 3t1
.. Preferably, it is in the range of 000. The number average molecular weight in this case is expressed by a polystyrene equivalent value determined by gel vermation chromatography according to a conventional method. If the number average molecular weight is lower than 5.0 On, the water resistance, chemical resistance and weather resistance will be insufficient;
If the molecular weight is higher than 0.000, there is a problem in terms of spray workability due to stringiness.

本発明に於いて、パラメチルスチレンと他の共重合可能
な単量体との共重合体を得るには、公知の重合法が採用
できるが、好ましくは、溶液重合法が採用される。前記
した単量体を用い、溶剤としては、例工ばトルエン、キ
シレンの如き芳香族炭化水素、酢酸エチル、酢酸ブチル
の如きエステル類、メチルエチルケトン、メチルイソブ
チルケトンの如きケトン類、ブタノール、メタノールの
カキアルコール類を用いることが出来る。又重合開始剤
として、例えばアゾビスイソブチロニトリル、ベンゾイ
ルパーオキサイド、t−ブチルパーベンゾエートなどの
公知のラジカル開始剤の存在下に重合させるのが一般的
である。
In the present invention, to obtain a copolymer of paramethylstyrene and other copolymerizable monomers, any known polymerization method can be employed, but preferably a solution polymerization method is employed. The above-mentioned monomers are used, and the solvent is, for example, aromatic hydrocarbons such as toluene and xylene, esters such as ethyl acetate and butyl acetate, ketones such as methyl ethyl ketone and methyl isobutyl ketone, butanol and methanol. Alcohols can be used. The polymerization is generally carried out in the presence of a known radical initiator such as azobisisobutyronitrile, benzoyl peroxide, or t-butyl perbenzoate.

かくして得られるアクリルラッカーは、適当なシンナー
で希釈してそのままクリヤー塗料として使用することも
可能であり、更に必要に応じて顔料、塗料用添加剤およ
び繊維素化合物の1種または2種以上を適宜併用する形
で混合使用することも出来る。顔料としては、酸化チタ
ン、ベンガラ、炭カル等の無機系顔料等および有機系顔
料等塗料分野において慣用的に用いられる顔料が挙げら
れる。
The acrylic lacquer obtained in this way can be diluted with a suitable thinner and used as a clear paint, and if necessary, one or more of pigments, paint additives, and cellulose compounds may be added as appropriate. They can also be used in combination. Examples of the pigment include pigments conventionally used in the paint field, such as inorganic pigments such as titanium oxide, red iron oxide, and carbonaceous pigments, and organic pigments.

また、塗料用添加剤としては、消泡剤、レベリング剤、
紫外線吸収剤、酸化防止剤、顔料分散助剤の如き公知の
塗料用添加剤の使用量で使用される。
In addition, additives for paint include antifoaming agents, leveling agents,
Known paint additives such as ultraviolet absorbers, antioxidants, and pigment dispersion aids are used in amounts.

更に繊維素系化合物としては、硝化綿やセルローズアセ
テートブチレートの如きものが挙げられる。
Furthermore, examples of cellulose compounds include nitrified cotton and cellulose acetate butyrate.

本発明のアクリルラッカーの塗装方法としては、刷毛塗
り、スプレー塗装またはロール塗装などの如き公知の方
法が採用出来る。
As a method for applying the acrylic lacquer of the present invention, known methods such as brush coating, spray coating, or roll coating can be employed.

上記した本発明のアクリルラッカーは、パラメチルスチ
レンの特定量を使用することにより、特に耐水性、耐候
性および耐薬品性に優れたものであり、且つ塗装性に優
れたものである。
The above-described acrylic lacquer of the present invention has particularly excellent water resistance, weather resistance, and chemical resistance, and has excellent paintability by using a specific amount of paramethylstyrene.

次に、本発明を実施例及び比較例により、説明するが、
特に断わりのない限り部又は%は重量を意味するものと
する。
Next, the present invention will be explained with reference to Examples and Comparative Examples.
Parts or percentages are by weight unless otherwise specified.

実施例1〜3及び比較例1〜4 攪拌装置、不活性ガス導入口、温度計及び冷却器を付設
した4ツロフラスコに、トルエン500g、及びブタノ
ール5009を仕込んだ後昇温しで98℃に上昇した時
点で、表1に示される混合物を各4時間にわたり滴下し
、その後も同温度に7時間保持して重合を行ない、目的
とする共重合物を得た。これらの共重合物の数平均分子
量の測定を行い、表】にまとめて示した。次いで、これ
らの各共重合物の 100部に対して、アルミペースト
(東洋アルミニウム(株)製、商品名1109MA)の
10部を加えて分散させたのち、酢酸エチル/’n−ブ
タノール/プチルセロンルブ=40/’40/20重合
比のシンナーでフォードカップ扁4により30秒になる
ように希釈してラッカーを調整した。
Examples 1 to 3 and Comparative Examples 1 to 4 After charging 500 g of toluene and 5009 butanol into a 4-ton flask equipped with a stirring device, an inert gas inlet, a thermometer, and a condenser, the temperature was raised to 98°C. At that point, the mixture shown in Table 1 was added dropwise over 4 hours each, and the same temperature was maintained for 7 hours to carry out polymerization to obtain the desired copolymer. The number average molecular weights of these copolymers were measured and summarized in Table 1. Next, to 100 parts of each of these copolymers, 10 parts of aluminum paste (manufactured by Toyo Aluminum Co., Ltd., trade name 1109MA) was added and dispersed, and then ethyl acetate/'n-butanol/butyl seron rub= The lacquer was prepared by diluting it with a thinner having a polymerization ratio of 40/'40/20 using a Ford cup flattener 4 for 30 seconds.

しかるのち、これをエアースプレーにより膜厚が15〜
18μになるようにボンデライト#144処理の0.6
朋の鉄板に塗装を行い、60℃で30分間焼付けを行っ
た。
After that, this was air-sprayed to a film thickness of 15~
0.6 of Bonderite #144 treatment to make it 18μ
I painted my iron plate and baked it at 60℃ for 30 minutes.

その後、常温にて3日間放置して得られたそれぞれの塗
膜について性能評価を行った。性能評価結果は表−2に
示す。
Thereafter, each coating film was left at room temperature for 3 days, and the performance of each film was evaluated. The performance evaluation results are shown in Table 2.

表 1 「註〕測定方法 光沢; JISK−5400による 60度鏡面光沢度試験方法に準じた。Table 1 "Note" Measurement method Gloss; according to JISK-5400 According to the 60 degree specular gloss test method.

エリクセン押し出し試験;エリクセン試験機により塗膜
にクラック等が生じない最大押し出しmm数で表示した
Erichsen extrusion test: Expressed as the maximum extrusion mm in which no cracks or the like occur in the coating film using an Erichsen tester.

耐水性;80℃の温水に24時間浸漬後直ちに引き上げ
原板との比較で目視判定した。
Water resistance: Immediately after being immersed in 80°C hot water for 24 hours, it was visually judged by comparison with the original plate.

耐候性試験; J IS −に−5400による耐候性
試験方法に準する。
Weather resistance test: Based on the weather resistance test method according to JIS-5400.

特許出願人 三井東圧化学株式会社patent applicant Mitsui Toatsu Chemical Co., Ltd.

Claims (1)

【特許請求の範囲】[Claims] (1) (A)ハラメチルスチレン5〜95重量%と(
B)他の共重合可能な単量体5〜95重量%とを共重合
して得られる数平均分子量5,000〜50.000で
ある共重合体および必要に応じて顔料、塗料用添加剤お
よび繊維系化合物の1種または2種以上を併用すること
を特徴とするアクリルラッカー。
(1) (A) 5 to 95% by weight of halamethylstyrene and (
B) A copolymer having a number average molecular weight of 5,000 to 50,000 obtained by copolymerizing with 5 to 95% by weight of other copolymerizable monomers, and pigments and paint additives as necessary. and an acrylic lacquer characterized by using one or more types of fiber-based compounds in combination.
JP13510783A 1983-07-26 1983-07-26 Acrylic lacquer Pending JPS6028459A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13510783A JPS6028459A (en) 1983-07-26 1983-07-26 Acrylic lacquer

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13510783A JPS6028459A (en) 1983-07-26 1983-07-26 Acrylic lacquer

Publications (1)

Publication Number Publication Date
JPS6028459A true JPS6028459A (en) 1985-02-13

Family

ID=15143996

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13510783A Pending JPS6028459A (en) 1983-07-26 1983-07-26 Acrylic lacquer

Country Status (1)

Country Link
JP (1) JPS6028459A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8646568B2 (en) 2010-12-28 2014-02-11 Denso Corporation Electric motor assembly and electric power steering device

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS53129285A (en) * 1977-04-19 1978-11-11 Nippon Oil Co Ltd Preparation of resin
JPS5655411A (en) * 1979-09-24 1981-05-16 Mobil Oil Ultraviolet resistant paraamethylstyrene copolymer
JPS5730711A (en) * 1980-06-19 1982-02-19 Basf Ag Copolymer and water-dilutable binder made therefrom for physically dry composition

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS53129285A (en) * 1977-04-19 1978-11-11 Nippon Oil Co Ltd Preparation of resin
JPS5655411A (en) * 1979-09-24 1981-05-16 Mobil Oil Ultraviolet resistant paraamethylstyrene copolymer
JPS5730711A (en) * 1980-06-19 1982-02-19 Basf Ag Copolymer and water-dilutable binder made therefrom for physically dry composition

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8646568B2 (en) 2010-12-28 2014-02-11 Denso Corporation Electric motor assembly and electric power steering device

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