JPS603624A - Photosensitive composition - Google Patents

Photosensitive composition

Info

Publication number
JPS603624A
JPS603624A JP11233483A JP11233483A JPS603624A JP S603624 A JPS603624 A JP S603624A JP 11233483 A JP11233483 A JP 11233483A JP 11233483 A JP11233483 A JP 11233483A JP S603624 A JPS603624 A JP S603624A
Authority
JP
Japan
Prior art keywords
photosensitive composition
composition
resin
alkali
acrylate
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
JP11233483A
Other languages
Japanese (ja)
Other versions
JPH0336210B2 (en
Inventor
Takao Ono
隆生 大野
Ginya Ishii
石井 銀弥
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to JP11233483A priority Critical patent/JPS603624A/en
Publication of JPS603624A publication Critical patent/JPS603624A/en
Publication of JPH0336210B2 publication Critical patent/JPH0336210B2/ja
Granted legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03FPHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/004Photosensitive materials
    • G03F7/027Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
    • G03F7/032Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with binders

Abstract

PURPOSE:To obtain an alkali-soluble ultraviolet-curing photosensitive composition emitting hardly a foul odor, undergoing little change with the lapse of time, and having superior acid resistance by mixing novolak resin having low mol.wt. with a compound having an alcoholic hydroxyl group and a polymerizable double bond and a photopolymn. initiator. CONSTITUTION:Novolak resin (A) having <=2,000mol.wt. such as phenol resin or cresol resin is mixed with a compound (B) having at least one alcoholic hydroxyl group and one polymerizable double bond in the molecule such as 2-hydroxymethyl acrylate or diethylene glycol monoacrylate and a photopolymn. initiator (C) such as benzoin or benzophenone to obtain the desired photosensitive composition. This composition is suitable for use as an etching resist, a plating resist and filling ink, and it is widely applied by making use of the superior acid resistance and solubility in alkali.

Description

【発明の詳細な説明】 本発明はエツチングレジスト、メツキレシスト及び穴埋
めインクとして使用されるインキ組成物、特に紫外線照
射により硬化し、その硬化塗膜がアルカリ水溶液により
溶解除去可能な感光性インキ組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an ink composition used as an etching resist, a metskire resist, and a hole-filling ink, and particularly to a photosensitive ink composition that is cured by ultraviolet irradiation and whose cured coating film can be dissolved and removed by an aqueous alkaline solution. .

印刷回路板や部分メッキ製品の製造工程においては被印
刷物(銅張積層板)や被メッキ品にスクリーン印刷、オ
フセット印刷等の手法によりエツチングレジスト又はメ
ツキレシストとして成膜性の付キを印刷して所望のパタ
ーン*i’;膜を形成した後、酸性のエツチング液又は
メッーキ液に浸漬して塗膜の形成されていない露出7;
ts分をエツチング又はメッキし、ついでアルカリ水溶
液に浸漬して塗膜を除去する操作が行7cわれる。従っ
てこの株のインキには塗膜として1月酸性であること、
アルカリ水溶液で塗膜が1rzIJHに除去できること
が要求される。従来上としてエツチングレジストに用い
られて来たインキ+i:i、を酸物としてはロジン、マ
レイン敲変性ロジン、フェノールノゼラック樹脂等のア
ルカリ可C谷)コL樹脂を溶剤に溶解したものが知られ
ている。これらは溶剤を揮発させて塗膜の形成ヶ行りも
ので、一般には熱乾燥型エツチングレジストと呼ばれて
いる。このタイプのエツチングレジストは比較的解像性
は良いが鉛蔽硬度がHB以下ど低いため、印刷回路基板
加工工程において傷か入り易く、この為、断線不良も起
り易い。又印刷工程においてはインキ中の溶剤が揮発し
て枯度が上昇したり、スクリーン印刷の場合はスクリー
ンが乾燥して目詰りが起り、印刷パターンにピンホール
やカスレ等が生じて鮮明な回路パターンが得られ難い。
In the manufacturing process of printed circuit boards and partially plated products, a film-formable mark is printed on the substrate (copper-clad laminate) or plated product as an etching resist or metal resist using methods such as screen printing or offset printing to produce the desired results. Pattern *i'; after forming a film, it is immersed in an acidic etching solution or plating solution, and no coating film is formed; exposure 7;
An operation 7c is performed in which the ts portion is etched or plated, and then the coating film is removed by immersion in an alkaline aqueous solution. Therefore, the ink of this strain must be acidic as a coating film,
It is required that the coating film can be removed to 1rzIJH with an alkaline aqueous solution. Ink +i:i, which has conventionally been used for etching resists, is known to be prepared by dissolving alkaline resins such as rosin, maleic denatured rosin, and phenolic noselac resins in solvents. It is being These resists form a coating film by volatilizing a solvent, and are generally called heat-drying etching resists. Although this type of etching resist has relatively good resolution, its lead shielding hardness is as low as HB or less, so it is easily scratched during the printed circuit board processing process, and is therefore prone to disconnection defects. In addition, during the printing process, the solvent in the ink evaporates and dryness increases, and in the case of screen printing, the screen dries and becomes clogged, causing pinholes and scratches in the printed pattern, making it difficult to see clear circuit patterns. is difficult to obtain.

更に硬化塗膜を得る為には80℃で3〜5分程度の乾燥
が必要となり、この為エネルギーの損失や溶剤による引
火の危険性及び環境汚染等の問題が残る。そこでこれら
の欠点を解消する為、近年・7、雪外線硬化型のインキ
が提案されている(特開昭56−8417号公+1)。
Furthermore, in order to obtain a cured coating film, drying at 80° C. for about 3 to 5 minutes is required, which leaves problems such as energy loss, the risk of ignition by the solvent, and environmental pollution. In order to eliminate these drawbacks, a snow line hardening type ink has recently been proposed (Japanese Patent Application Laid-Open No. 56-8417+1).

しかしこの提案のインキ組成物ではスチレン−マレイン
酸共重合体を使用していることから、臭気が強い上、目
、鼻等の粘膜に強い刺激を与えるので好ましくない。ま
た経時的にインキの粘度変化が生じたり、硬化条件によ
りアルカリ水溶液に対する硬化塗膜の溶解度が減少して
1影潤剥離を起すなどの欠点もあり、十分に満足し得る
ものではない。
However, since the proposed ink composition uses a styrene-maleic acid copolymer, it not only has a strong odor, but also causes strong irritation to the mucous membranes of the eyes, nose, etc., and is therefore undesirable. In addition, there are also drawbacks such as changes in the viscosity of the ink over time, and depending on the curing conditions, the solubility of the cured coating film in an alkaline aqueous solution decreases, resulting in peeling due to one shadow, so that it is not fully satisfactory.

本発明の目的は臭気や粘膜に対する刺激が少なく、経時
によるインキの特性変化や硬化条件による塗膜の特性変
化も少なく、しかも耐酸性に優れ、印刷特性が良好で、
且つ硬度の高い硬°化塗膜を形成し得るアルカリ溶解型
紫外線硬化型感光性インキ組成物ン提供することである
The purpose of the present invention is to provide a material with little odor and irritation to mucous membranes, little change in ink characteristics over time and changes in coating film characteristics due to curing conditions, excellent acid resistance, and good printing characteristics.
Another object of the present invention is to provide an alkali-soluble ultraviolet curable photosensitive ink composition capable of forming a hardened coating film with high hardness.

本発明の′感光性組成物は(a)分子量が2000以下
のノゼラック樹脂と(b1分子内に少くとも1個のアル
コール性水酸基及び1個の重合性二重結合を有する化合
物と(C1光沌合開始剤とを主成分とするもので、紫外
線により硬化し、且つこの硬化部が水性アルカリに可溶
であることを特徴とするものである。
The photosensitive composition of the present invention comprises (a) a Nozelac resin having a molecular weight of 2,000 or less; (b) a compound having at least one alcoholic hydroxyl group and one polymerizable double bond in the molecule; It is characterized in that it is cured by ultraviolet rays and that the cured portion is soluble in aqueous alkali.

本発明の感光性組成物は硬化堕膜が耐r戊性に優れ、且
つアルカリ可溶であることから、エツチングレジストや
メツキレシスト及び穴埋めインクとしてば力)りでなく
、このようン工イ快化1Z、ミm:’;+。
Since the photosensitive composition of the present invention has a cured fallen film that has excellent resistance to scratching and is soluble in alkali, it can be used not only as an etching resist, as a masking resist, and as a hole-filling ink, but also as an easy-to-use material. 1Z, Mi m:';+.

の特性を利用したあらゆる用途に適用できる。It can be applied to any application that utilizes the characteristics of

本発明に使用される(a)のノボラックaJ ]i’J
とは水性アルカリに可溶のフェノール樹脂、クレゾール
樹脂及びアルキルフェノール位(脂をいう。 へ分子量
は2000以上では硬化が悪くなるので、2000以下
が好ましい。
Novolak aJ of (a) used in the present invention ]i'J
refers to aqueous alkali-soluble phenolic resins, cresol resins, and alkylphenol resins (fats).If the molecular weight is 2,000 or more, curing will be poor, so a molecular weight of 2,000 or less is preferable.

(b)の分子内に少くとも1個のアルコール性水酸基及
び1個の二重結合な有する化合物としては2−ヒドロキ
シメチ迭アクリレート、2−ヒドロキシエチルアクリレ
ート、2−ヒト90キシプロピルアクリレート、3−ヒ
ドロキシプロピルアクリレート、2−ヒドロキシ−3−
クロルプロピルアクリレート、2−ヒドロキシブチルア
クリレート、ジエチレングリコール七ノアクリレート及
びこれらに対応するブタン1)レートが挙げられる。添
加縫は(a)成分に対し20〜70wt、係が好ましく
、こθ〕範囲以外でQ家?匣(ヒ性が悪く、硬化塗膜の
l104エツチング性も8X−・。
Compounds having at least one alcoholic hydroxyl group and one double bond in the molecule of (b) include 2-hydroxymethacrylate, 2-hydroxyethyl acrylate, 2-human 90xypropyl acrylate, 3- Hydroxypropyl acrylate, 2-hydroxy-3-
Mention may be made of chloropropyl acrylate, 2-hydroxybutyl acrylate, diethylene glycol heptanoacrylate and their corresponding butane 1) acrylates. It is preferable for the additive stitch to have a weight of 20 to 70 wt relative to the component (a). Box (has poor arsenic resistance, and l104 etching resistance of the cured coating is 8X-.

次に(c)の光重合開始剤としてはペンツ°イン、ブチ
ロイン、アセトイン等のα−刀ルゼニルアルコール類;
ベンゾインメチルニー・チル、ベンゾインエチルエーテ
ル、ペンゾインインフ”ロビルエーテル、ペンゾインイ
ソフ′チルエーテル、ビバロインエチルエーテル等ノア
シロインエーテル頌;ジアセチル、ジペンソ9イル、ジ
フェニルケトン、フェニルグリオキサール、2.3−ペ
ンメジオン、1−フェニルブタン−1,2−ジオン、2
,3−オクタジオン、ジフェニルトリケトン等の隣接ポ
リケトン化合物頷;ベンゾフェノン、′ω−ブロムアセ
トフェノン、2−ヒドロキシ−2−メチルプロピオフェ
ノン、4′−イソプロビル−2−ヒドロキシ−2−メチ
ルプロピオフェノン、2,2−ジメトキシ−2−フェニ
ルアセトフェノン、p −tert−ブチルトリクロロ
アセトフェノン、p −tart−ブチルモノクロロア
セトフェノン、2 、2’−ジェトキシアセトフェノン
、4 、4’−ビス−ジアルキルアミノベンゾフェノン
、2,2−ジメトキシ−2−フェニルアセトフェノン等
のフェノン’fA %が2hげられる。
Next, as the photopolymerization initiator (c), α-alcohols such as pentuin, butyroin, acetoin, etc.;
Benzoin methyl ni-thyl, benzoin ethyl ether, penzoin inf'robyl ether, penzoin isof'thyl ether, bivaloin ethyl ether, etc. Noacyloin ethers; diacetyl, dipenso-9yl, diphenyl ketone, phenylglyoxal, 2.3-penmedione, 1- Phenylbutane-1,2-dione, 2
Adjacent polyketone compounds such as , 3-octadione, diphenyltriketone; benzophenone, 'ω-bromoacetophenone, 2-hydroxy-2-methylpropiophenone, 4'-isopropyl-2-hydroxy-2-methylpropiophenone , 2,2-dimethoxy-2-phenylacetophenone, p-tert-butyltrichloroacetophenone, p-tart-butylmonochloroacetophenone, 2, 2'-jethoxyacetophenone, 4, 4'-bis-dialkylaminobenzophenone, 2, Phenone 'fA% such as 2-dimethoxy-2-phenylacetophenone is obtained for 2 h.

以上の(a)、(b)、(C)3成分の端的な割合は使
用目的によって若干変動するが、(a)成分については
(bl成分に対して30〜70wt、憾、(b)成分に
ついては(a)成分に対して30〜70 wL、 4、
(c)成分については(al +(b)の合計敬に対し
て2〜15 wt、 %が適当である。(&)成分の割
合力’ib)成分に対して30wt、%以下か70 w
t、4以上では硬化速度が遅くなったり内部硬化不良を
起して耐薬品性が不十分と1よる。また(c1成分の割
合が2 wt0%以下では硬化速度が遅くなる上、内部
硬化不良を起して塗膜の耐薬品性が悪くなる。
The exact proportions of the three components (a), (b), and (C) above vary slightly depending on the purpose of use, but for the (a) component, it is 30 to 70 wt relative to the bl component; For component (a), 30 to 70 wL, 4,
For component (c), 2 to 15 wt, % is appropriate for the total weight of (al + (b)).
If t is 4 or more, the curing speed becomes slow or internal curing failure occurs, resulting in insufficient chemical resistance. Furthermore, if the ratio of the c1 component is less than 2 wt 0%, the curing speed will be slow and internal curing will be poor, resulting in poor chemical resistance of the coating film.

一方(c)成分の割合が15%以上では特性の向上が見
られず不経済である。
On the other hand, if the proportion of component (c) is 15% or more, no improvement in properties is observed and it is uneconomical.

本発明の組成物には通常この分野で使用される各種添加
物、例えば改質剤、粘度調整剤、アルカリ除去促進剤、
充填剤、チクソトロピー剤、レベリング剤、着色剤、熱
重合禁止剤、消泡剤等を添加することができる。
The composition of the present invention contains various additives commonly used in this field, such as modifiers, viscosity modifiers, alkali removal promoters,
Fillers, thixotropic agents, leveling agents, colorants, thermal polymerization inhibitors, antifoaming agents, etc. can be added.

改質剤としてはキシレン樹脂、ロジン、ロジン変性樹脂
、アクリル系共重合体、スチレン−マレイン酸共重合体
等がある。これらの使用量は組成I吻に対して1〜30
 wt、 4であり、主としては膜の密着性、レベリン
グ、耐薬品性等の同上を目的として添加される。
Examples of the modifier include xylene resin, rosin, rosin modified resin, acrylic copolymer, and styrene-maleic acid copolymer. The amount used is 1 to 30 for composition I snout.
wt, 4, and is added mainly for the same purposes as the above, such as film adhesion, leveling, and chemical resistance.

粘度MLf4整剤としてはメトキシエチルアクリレート
、エトキシエチルアクリレート、メトキシエチルアクリ
レート、メトキシエチルアクリレート、テトラヒドロア
クリレート、ベンジルアクリレート、フェノキシエチル
アクリレート、シクロヘキ′シルアクリレート、カルピ
トールアクリレート及びこれらに相当するメタクリレー
トが挙げられる。これらの使用量は組成物に対して通常
20 wt、 4以下である。アルカリ除去促進剤、塗
膜硬度の向上剤としてはイタコ/■♀、メチルへキサヒ
ドロフタル酸、3−メチルテトラヒドロフタル酸、4−
メチルテトラヒドロフiA’H% コハク9、メチルへ
Φサヒドロフタル酸及びそれらの酸無水物と2−ヒドロ
キシエチルアクリレート(又はメタクリレート)或いは
2−ヒドロキシエチルアクリレート(又はメタクリレー
ト)等、分子内に少くとも1個のアルコール性水酸基及
び1個の重合性二重結合を有する化合物等とで形成され
るモノエステル化物が挙げられる。これらの使用量は組
成物に対して通常40 wt、4以下である。
Examples of the viscosity MLf4 modifier include methoxyethyl acrylate, ethoxyethyl acrylate, methoxyethyl acrylate, methoxyethyl acrylate, tetrahydroacrylate, benzyl acrylate, phenoxyethyl acrylate, cyclohexyl acrylate, carpitol acrylate, and methacrylates corresponding to these. The amount of these used is usually 20 wt.4 or less relative to the composition. As alkali removal accelerators and coating film hardness improvers, itaco/■♀, methylhexahydrophthalic acid, 3-methyltetrahydrophthalic acid, 4-
Methyltetrahydrophthalic acid and its acid anhydrides and 2-hydroxyethyl acrylate (or methacrylate) or 2-hydroxyethyl acrylate (or methacrylate), etc., at least one in the molecule Examples include monoesterified products formed with a compound having an alcoholic hydroxyl group and one polymerizable double bond. The amount of these used is usually 40 wt, 4 or less based on the composition.

充填剤としてはメルク、硫酸バリウム、クレー、シリカ
等がある。これらの使用量は組成物に対して通常1〜5
0 wt、 %である。
Examples of fillers include Merck, barium sulfate, clay, and silica. The amount of these used is usually 1 to 5 based on the composition.
0 wt, %.

チクソトロピー剤としてはアエロシールナ100アエロ
シール≠200、アエロシールR−972(日本アエロ
ジル(株)iAA)のシリカ系化合物やオルガナイ)A
((株)豊順洋行製)のようなモンモリナイトの有機塩
基複合体等がある。これらの使用量は組成物に対し通常
1〜5wt、%である。
As thixotropic agents, Aerosilna 100, Aerosil ≠ 200, Aerosil R-972 (Nippon Aerosil Co., Ltd. iAA) silica-based compounds and Organai) A
There are organic base complexes of montmorinite such as (manufactured by Toyojun Yoko Co., Ltd.). The amount of these used is usually 1 to 5% by weight based on the composition.

着色剤としてはフタロシアニン系、スレン系等の顔料及
びメチルバイオレット、メチレンブルー等の染料がある
。これらの使用量は組成物に対し通常02〜3wt−%
である。
Examples of colorants include phthalocyanine-based pigments, threne-based pigments, and dyes such as methyl violet and methylene blue. The amount of these used is usually 02 to 3 wt-% based on the composition.
It is.

SXCXC合剤止剤てはノ〜イドロキノン、p−メトキ
シフェノール、塩化第一銅、ナフチルアミン等がある。
Examples of the SXCXC mixture inhibitor include nohydroquinone, p-methoxyphenol, cuprous chloride, and naphthylamine.

これらの使用量は組成物に対し通常0.001〜0.1
 wt、係である。
The amount of these used is usually 0.001 to 0.1 based on the composition.
wt, I'm in charge.

消泡剤としては TSA−720,TSA−750゜Y
SA−02(東芝シリコン(株)製)等のシリコーン系
消泡剤や弗素系界面活性剤がある。これらの使用量は組
成物に対し曲常0.5− 2 wt、 %である。
As an antifoaming agent, TSA-720, TSA-750゜Y
There are silicone antifoaming agents such as SA-02 (manufactured by Toshiba Silicon Co., Ltd.) and fluorine surfactants. The amount of these used is typically 0.5-2% by weight based on the composition.

以下に本発明を実施例によって(に詳νもず・ニン。The present invention will now be explained in more detail by way of examples.

フェノールノゼヲツク樹脂の合成: フェノール類 50 50 ホルマリン 47 47 蓚 酸 1.3 1.8 塩 酸 1.2 i、 2 製造方法: マスフェノール類とホルマリン′とf^FIZとを反応
器に仕込み、還流温度で60分間反応させ、次に塩酸を
加えてさらに35分間縮合させる。
Synthesis of phenolic nose resin: Phenols 50 50 Formalin 47 47 Oxalic acid 1.3 1.8 Hydrochloric acid 1.2 i, 2 Production method: Mass phenols, formalin' and f^FIZ are charged in a reactor, React for 60 minutes at reflux temperature, then add hydrochloric acid and condense for a further 35 minutes.

冷水を多量添加して反応を停止し、30分曲fil(置
する。次に減圧脱水を行ない、その後、Cットに得られ
た樹脂液を流して固まらせる。
The reaction is stopped by adding a large amount of cold water, and the mixture is left to stand for 30 minutes. Next, dehydration is performed under reduced pressure, and then the resin liquid obtained is poured into a container to solidify.

実施例1 下記処決の感光性組成物を調製しtこ。Example 1 A photosensitive composition having the following treatment was prepared.

ノエノールノボラツク樹脂(合成例2) 30wt、%
2−ヒドロキシエチルメタクリレート 30 〃フタロ
シアニンブル−〇、5 wt、qb2−ヒドロキシ−2
−メチルプロピオフェノン 3 〃硫酸バリウム 36
.5 tt 比紋例1 実施例1に2いて、2−ヒドロキシエチルメタクリレー
トのみをカルピトールアクリレートに変えて感光性組成
物を調製した。
Noenol novolac resin (synthesis example 2) 30wt, %
2-Hydroxyethyl methacrylate 30 Phthalocyanine blue-○, 5 wt, qb2-hydroxy-2
-Methylpropiophenone 3 Barium sulfate 36
.. 5 tt Ratio Example 1 A photosensitive composition was prepared in Example 1 and 2 except that only 2-hydroxyethyl methacrylate was replaced with carpitol acrylate.

比較例2 実施例2に訃いて 2−ヒドロキシエチルメタクリレー
トのみを1,3−プクンジオールアクリレートに変えて
感光性組成物を調製した。
Comparative Example 2 A photosensitive composition was prepared in accordance with Example 2 except that only 2-hydroxyethyl methacrylate was replaced with 1,3-pukundiol acrylate.

実施例2 下記処決の感光性組成物を調製した。Example 2 A photosensitive composition having the following treatment was prepared.

フェノールノボラック樹脂(合成例1) 20wt、4
2−メメクロキシエチルアシット’−+ナヒドロフタレ
ート 10 〃2〜ヒドロキシプロピルアクリレート 
40 〃フタロシアニンブルー 0.5〃 2.2−ジェトキシアセトフェノン 5 〃モダフロー
(モンサント社製しベリンク剤) 3 、ttシリカ 
24.5 7/ 比較例3 実施例2において、2−ヒドロキシプロピルメタクリレ
ートのみをベンジルアクリレートに変えて感光性組成物
を調製し4こ。
Phenol novolak resin (synthesis example 1) 20wt, 4
2-memecloxyethyl acit'-+nahydrophthalate 10 2-hydroxypropyl acrylate
40 〃Phthalocyanine Blue 0.5〃 2.2-Jethoxyacetophenone 5 〃Modaflow (Belink agent manufactured by Monsanto) 3, tt silica
24.5 7/ Comparative Example 3 A photosensitive composition was prepared in Example 2 except that only 2-hydroxypropyl methacrylate was replaced with benzyl acrylate.

比較例4 実施例2において、2−ヒドロキシプロピルメタクリレ
ートのみをテトラエチレングリコールに変えて感光性組
成物を調製した。
Comparative Example 4 A photosensitive composition was prepared in Example 2 except that only 2-hydroxypropyl methacrylate was replaced with tetraethylene glycol.

次に以上の感光性組成物をインキとして苗(T’な銅張
積層板にスクリーン印刷により20μnLの膜厚となる
よう印刷塗布し、これを強凡80W/cIrLのオゾン
レス集光型高圧水銀灯を” 16j 1!:’iiえた
紫外線硬化炉中、sm/分の速度でNyx j:ilJ
きせながら、照射距離10CrILで紫外線照射して?
fミ膜を硬化させ、この硬化塗膜について鉛”ill 
4Qi、!p:、’l、アルカリ浴解性及び耐エツチン
グ性な試J6 した。
Next, the above photosensitive composition was applied as an ink to a seedling (T') copper-clad laminate by screen printing to a film thickness of 20 μnL, and this was applied using an ozone-less concentrating high-pressure mercury lamp of 80 W/cIrL. ” 16j 1!:'ii Nyx j:ilJ at a speed of sm/min in a UV curing oven
Is it irradiated with ultraviolet rays at an irradiation distance of 10 CrIL?
The film is cured and the cured film is treated with lead”ill.
4 Qi,! p:,'l, alkaline bath dissolution and etching resistance test J6.

また感光性組成物(インキ)についてもイ’、+:存安
定性を試験した。これらの試験方法は下記のと 1おり
である。
The photosensitive compositions (inks) were also tested for stability (A', +). These test methods are as follows.

鉛筆硬度: 硬化塗膜試片の塗膜上に市販の鉛筆(三菱鉛筆(株)製
ユニ)を当てその上に1ゆの荷重をかけて塗膜に傷が入
った時の硬度をめる。
Pencil hardness: Place a commercially available pencil (Uni manufactured by Mitsubishi Pencil Co., Ltd.) on the paint film of a cured paint film sample, apply a 1-Yu load on it, and measure the hardness when the paint film is scratched. .

アルカリ溶解性: 硬化塗膜試片の塗膜面に39g水酸化ナトリウムを吹き
付けて塗膜が溶解する迄の時間をめる。
Alkali solubility: Spray 39g of sodium hydroxide onto the coating surface of a cured coating sample and measure the time until the coating dissolves.

耐エツチング液性: 塩化第一銅40wt、係、塩酸10 wt、チ及び水5
0 wt0%よりなる50℃のエツチング液に硬化塗膜
試片な30分間浸漬し、塗膜の状態を目視で観察する。
Etching liquid resistance: cuprous chloride 40wt, hydrochloric acid 10wt, water 5wt
A specimen of the cured coating film was immersed in an etching solution of 0 wt% at 50° C. for 30 minutes, and the condition of the coating film was visually observed.

保存安定性: 感光性組成物50gを容器50ccの茶色のポリ容器に
入れ、70℃の恒温槽中に放置して組成物がゲル化する
迄の時間をめる。
Storage stability: 50 g of the photosensitive composition is placed in a 50 cc brown plastic container and left in a constant temperature bath at 70° C. to allow time for the composition to gel.

試験結果は下表の通りである。The test results are shown in the table below.

Claims (1)

【特許請求の範囲】 1、(a)分子量が2000以下のノゼラツク樹脂と(
b)分子内に少くとも1個のアルコール性水酸基及び1
個の重合性二重結合を有する化合物と(e)光重合開始
剤とを主成分とする感光性組成物。 2、光1合開始剤がフ二ノン系である特許請求の範囲第
1項記載の組成物。
[Scope of Claims] 1. (a) Nozerak resin having a molecular weight of 2000 or less and (
b) At least one alcoholic hydroxyl group and one
A photosensitive composition containing as main components a compound having 1 or more polymerizable double bonds and (e) a photopolymerization initiator. 2. The composition according to claim 1, wherein the photo-initiator is a funinone type.
JP11233483A 1983-06-22 1983-06-22 Photosensitive composition Granted JPS603624A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11233483A JPS603624A (en) 1983-06-22 1983-06-22 Photosensitive composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11233483A JPS603624A (en) 1983-06-22 1983-06-22 Photosensitive composition

Publications (2)

Publication Number Publication Date
JPS603624A true JPS603624A (en) 1985-01-10
JPH0336210B2 JPH0336210B2 (en) 1991-05-30

Family

ID=14584077

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11233483A Granted JPS603624A (en) 1983-06-22 1983-06-22 Photosensitive composition

Country Status (1)

Country Link
JP (1) JPS603624A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1150165A1 (en) * 2000-04-25 2001-10-31 JSR Corporation Radiation sensitive resin composition for forming barrier ribs for an el display element, barrier ribs and el display element

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55127097A (en) * 1979-03-20 1980-10-01 Matsushita Electric Ind Co Ltd Photocurable resin composition and solder resist
JPS5825371A (en) * 1981-08-06 1983-02-15 Toyobo Co Ltd Ultraviolet-curing ink composition for printed circuit

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55127097A (en) * 1979-03-20 1980-10-01 Matsushita Electric Ind Co Ltd Photocurable resin composition and solder resist
JPS5825371A (en) * 1981-08-06 1983-02-15 Toyobo Co Ltd Ultraviolet-curing ink composition for printed circuit

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1150165A1 (en) * 2000-04-25 2001-10-31 JSR Corporation Radiation sensitive resin composition for forming barrier ribs for an el display element, barrier ribs and el display element
KR20010098809A (en) * 2000-04-25 2001-11-08 마쯔모또 에이찌 Radiation sensitive resin composition for forming barrier ribs for an EL display element, barrier rib and EL display element

Also Published As

Publication number Publication date
JPH0336210B2 (en) 1991-05-30

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