JP4771473B2 - ポジ型感光性組成物 - Google Patents
ポジ型感光性組成物 Download PDFInfo
- Publication number
- JP4771473B2 JP4771473B2 JP2006115337A JP2006115337A JP4771473B2 JP 4771473 B2 JP4771473 B2 JP 4771473B2 JP 2006115337 A JP2006115337 A JP 2006115337A JP 2006115337 A JP2006115337 A JP 2006115337A JP 4771473 B2 JP4771473 B2 JP 4771473B2
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- Prior art keywords
- photosensitive composition
- positive photosensitive
- resin
- component
- copolymer
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims description 48
- 229920001577 copolymer Polymers 0.000 claims description 42
- -1 polyglycerin Chemical compound 0.000 claims description 40
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- 239000000126 substance Substances 0.000 claims description 32
- 229920000642 polymer Polymers 0.000 claims description 25
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 18
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 17
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- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 12
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- 238000004090 dissolution Methods 0.000 claims description 10
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- KIUKXJAPPMFGSW-DNGZLQJQSA-N (2S,3S,4S,5R,6R)-6-[(2S,3R,4R,5S,6R)-3-Acetamido-2-[(2S,3S,4R,5R,6R)-6-[(2R,3R,4R,5S,6R)-3-acetamido-2,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-2-carboxy-4,5-dihydroxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid Chemical compound CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](O[C@H]3[C@@H]([C@@H](O)[C@H](O)[C@H](O3)C(O)=O)O)[C@H](O)[C@@H](CO)O2)NC(C)=O)[C@@H](C(O)=O)O1 KIUKXJAPPMFGSW-DNGZLQJQSA-N 0.000 claims description 8
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- HDTRYLNUVZCQOY-WSWWMNSNSA-N Trehalose Natural products O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 HDTRYLNUVZCQOY-WSWWMNSNSA-N 0.000 claims description 4
- HDTRYLNUVZCQOY-LIZSDCNHSA-N alpha,alpha-trehalose Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 HDTRYLNUVZCQOY-LIZSDCNHSA-N 0.000 claims description 4
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- 239000000463 material Substances 0.000 claims description 2
- JMHCCAYJTTWMCX-QWPJCUCISA-M sodium;(2s)-2-amino-3-[4-(4-hydroxy-3,5-diiodophenoxy)-3,5-diiodophenyl]propanoate;pentahydrate Chemical compound O.O.O.O.O.[Na+].IC1=CC(C[C@H](N)C([O-])=O)=CC(I)=C1OC1=CC(I)=C(O)C(I)=C1 JMHCCAYJTTWMCX-QWPJCUCISA-M 0.000 claims description 2
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- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 16
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- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 14
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- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 12
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- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 9
- 125000000217 alkyl group Chemical group 0.000 description 9
- 229910052802 copper Inorganic materials 0.000 description 9
- 239000010949 copper Substances 0.000 description 9
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 9
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- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 8
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- 229910052782 aluminium Inorganic materials 0.000 description 8
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- 125000001424 substituent group Chemical group 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
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- 125000005037 alkyl phenyl group Chemical group 0.000 description 4
- 229910000365 copper sulfate Inorganic materials 0.000 description 4
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 4
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Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
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- B41C—PROCESSES FOR THE MANUFACTURE OR REPRODUCTION OF PRINTING SURFACES
- B41C1/00—Forme preparation
- B41C1/10—Forme preparation for lithographic printing; Master sheets for transferring a lithographic image to the forme
- B41C1/1008—Forme preparation for lithographic printing; Master sheets for transferring a lithographic image to the forme by removal or destruction of lithographic material on the lithographic support, e.g. by laser or spark ablation; by the use of materials rendered soluble or insoluble by heat exposure, e.g. by heat produced from a light to heat transforming system; by on-the-press exposure or on-the-press development, e.g. by the fountain of photolithographic materials
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/05—Alcohols; Metal alcoholates
- C08K5/053—Polyhydroxylic alcohols
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
- C08K5/101—Esters; Ether-esters of monocarboxylic acids
- C08K5/103—Esters; Ether-esters of monocarboxylic acids with polyalcohols
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring
- C08K5/3415—Five-membered rings
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L101/00—Compositions of unspecified macromolecular compounds
- C08L101/02—Compositions of unspecified macromolecular compounds characterised by the presence of specified groups, e.g. terminal or pendant functional groups
- C08L101/06—Compositions of unspecified macromolecular compounds characterised by the presence of specified groups, e.g. terminal or pendant functional groups containing oxygen atoms
- C08L101/08—Carboxyl groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L101/00—Compositions of unspecified macromolecular compounds
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Description
本発明のポジ型感光性組成物に、(D)光酸発生剤をさらに含有することが好適である。
本発明のポジ型感光性組成物に、(E)(1)ビニルピロリドン/酢酸ビニルコポリマー、(2)ビニルピロリドン/ジメチルアミノエチルメタクリレートコポリマー、(3)ビニルピロリドン/ビニルカプロラクタム/ジメチルアミノエチルメタクリレートコポリマー、(4)ポリ酢酸ビニル、(5)ポリビニルブチラール、(6)ポリビニルホルマール、(7)テルペンフェノール樹脂、(8)アルキルフェノール樹脂、(9)メラミン/ホルムアルデヒド樹脂、及び(10)ケトン樹脂からなる群から選択される少なくとも1種の樹脂をさらに含有することが好適である。
本発明のポジ型感光性組成物に、(F)トリアリールメタン系染料をさらに含有することが好ましい。
1.シリンダーに感光液塗布(ドライ膜厚2−5μmが好ましい。ピンホールを無くすため膜は厚い方が良いが、薄い方が使用量が少ない分コストは安くなる。)→2.乾燥(タッチドライまで15分→終了まで15〜20分)→3.露光(光源:半導体レーザー830nm、220mJ/cm2)→4.現像(60〜90秒/25℃)→5.水洗(スプレー30秒)→6.エッチング(深度10〜30μm、腐食 塩化第二銅水溶液、銅換算60g/L)→7.レジスト剥離(アルカリ剥離)→8.水洗→9.Crメッキ(水に対してクロム酸250g/L,硫酸2.5g/L)→10.水洗→11.印刷。
1.CTP(PS版)(アルミ研摩→感光液塗布→乾燥)→2.露光(光源:半導体レーザー830nm、220mJ/cm2)→3.現像→4.印刷。
表1に示す配合物質及び配合割合によりポジ型感光性組成物を調製し、テスト感光液とした。
樹脂A1:SMA 1440(SARTOMER社製,スチレン/無水マレイン酸共重合体のブチルセロソルブによる部分エステル化物)
赤外線吸収色素:前記式(3)で示される赤外線吸収色素
樹脂改質剤1:グリセリン
樹脂改質剤2:ソルビトール
溶解阻止剤:TrisP−PA(本州化学工業(株)製、前記式(7)で示される化合物)
光酸発生剤:IRGACURE(登録商標)250(チバ・スペシャルティ・ケミカルズ(株)製、前記式(8)で示される化合物)
樹脂E1:PVP/VAコポリマー(分子量46,000、ガラス転移点96℃のビニルピロリドンと酢酸ビニルの共重合体、ビニルピロリドン/酢酸ビニル 50/50)
着色色素:オイルブルー613(オリエント化学工業(株)製、Color Index(C.I.) No. 42595)
PM:プロピレングリコールモノメチルエーテル
IPA:イソプロピルアルコール
MEK:メチルエチルケトン
1)エッジの解像性
解像力テストパターンを用いて、市松模様、グレーチングの7.9μmの線のエッジがシャープかどうかを測定した。表中◎は良好な結果であり解像性が合格、×は画像なしで製版できず解像性が不合格。
2)現像ラチチュード
大日本印刷株式会社製のセル蔵(網点の開孔率自動測定のできる装置)を用いて測定を行った。現像の回数を多くしたテスト(本実施例では3回)により、7.9μm×7.9μmの露光により、セル面積計算で60−75μm2に入っている場合は、印刷濃度の許容範囲に入っている為、良好であり、表中◎で示した。印刷許容範囲外の場合を表中×で示した。
3)密着性
tesa test: DIN EN ISO 2409 tesaテープによる碁盤目密着性テストで100マスが全て残る場合を◎、20%未満の範囲で剥離される場合を○、20%以上剥離する場合を×とした。
4)感度
露光量をふり画像パターンに再現性が近いもので感度を決定。露光機はクレオ社のサーマルイメージングヘッドを用いた。
5)現像
残渣がなくなるまでの現像時間を測定した。
6)残膜率
塗膜の厚みを測定する装置であるFILMETRICS Thin Film Analyzer F20(Filmetrics Co製)を用いて、現像前の膜厚、現像後の膜厚を測定し、残膜率を算出した。
7)画像
オリジナル画像に再現性が近いかどうかを評価した。◎:非常に良好、×:非常に悪い、−:現像で画像が無くなる。
8)ひび割れ検査
感光膜にひび割れが発生したか否かを評価した。
Claims (9)
- (A)分子中に少なくとも1つのカルボキシル基を有する高分子物質、
(B)画像露光光源の赤外線を吸収して熱に変換する光熱変換物質、及び
(M)樹脂改質剤
を含有してなるポジ型感光性組成物であって、
前記樹脂改質剤(M)が、グリセリン、ジグリセリン、ポリグリセリン、ヒアルロン酸、ヒアルロン酸の塩、ソルビトール、プロピレングリコール、1,3−ブチレングリコール、エチレングリコール、ジエチレングリコール、果糖、ブドウ糖、オリゴ糖、オリゴ糖アルコール、マルチトール、トレハロース、還元澱粉加水分解物、グリシンベタイン、ピロリドンカルボン酸、ピロリドンカルボン酸塩及び乳酸ナトリウムからなる群から選択される一種又は二種以上であることを特徴とするポジ型感光性組成物。 - 前記樹脂改質剤(M)が、グリセリン又はソルビトールであることを特徴とする請求項1記載のポジ型感光性組成物。
- (C)溶解阻止剤をさらに含有することを特徴とする請求項1又は2記載のポジ型感光性組成物。
- (D)光酸発生剤をさらに含有することを特徴とする請求項1〜3のいずれか1項記載のポジ型感光性組成物。
- (E)(1)ビニルピロリドン/酢酸ビニルコポリマー、(2)ビニルピロリドン/ジメチルアミノエチルメタクリレートコポリマー、(3)ビニルピロリドン/ビニルカプロラクタム/ジメチルアミノエチルメタクリレートコポリマー、(4)ポリ酢酸ビニル、(5)ポリビニルブチラール、(6)ポリビニルホルマール、(7)テルペンフェノール樹脂、(8)アルキルフェノール樹脂、(9)メラミン/ホルムアルデヒド樹脂、及び(10)ケトン樹脂からなる群から選択される少なくとも1種の樹脂をさらに含有することを特徴とする請求項1〜4のいずれか1項記載のポジ型感光性組成物。
- (F)トリアリールメタン系染料をさらに含有することを特徴とする請求項1〜5のいずれか1項記載のポジ型感光性組成物。
- 請求項1〜6のいずれか1項記載のポジ型感光性組成物を用いることを特徴とするフォトファブリケーション方法。
- 印刷版、電子部品、精密機器部品、又は偽造防止用関連部材を製造するために適用されることを特徴とする請求項7記載のフォトファブリケーション方法。
- 請求項1〜6のいずれか1項記載のポジ型感光性組成物を用いた製版方法。
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