JPH0415096B2 - - Google Patents
Info
- Publication number
- JPH0415096B2 JPH0415096B2 JP10944782A JP10944782A JPH0415096B2 JP H0415096 B2 JPH0415096 B2 JP H0415096B2 JP 10944782 A JP10944782 A JP 10944782A JP 10944782 A JP10944782 A JP 10944782A JP H0415096 B2 JPH0415096 B2 JP H0415096B2
- Authority
- JP
- Japan
- Prior art keywords
- ink
- substrate
- inkjet recording
- recording head
- film
- 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.)
- Expired
Links
- 239000000758 substrate Substances 0.000 claims description 35
- 229920005989 resin Polymers 0.000 claims description 21
- 239000011347 resin Substances 0.000 claims description 21
- 229910052809 inorganic oxide Inorganic materials 0.000 claims description 15
- 150000004767 nitrides Chemical class 0.000 claims description 14
- 239000000976 ink Substances 0.000 description 53
- 239000010408 film Substances 0.000 description 24
- 229920002120 photoresistant polymer Polymers 0.000 description 18
- 238000000034 method Methods 0.000 description 15
- 239000000203 mixture Substances 0.000 description 15
- 239000010410 layer Substances 0.000 description 14
- 238000004519 manufacturing process Methods 0.000 description 10
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- 239000000853 adhesive Substances 0.000 description 6
- 230000001070 adhesive effect Effects 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 239000011521 glass Substances 0.000 description 5
- -1 Ta 2 O 5 Chemical class 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000005520 cutting process Methods 0.000 description 4
- 238000005530 etching Methods 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 3
- 239000011241 protective layer Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 229910004298 SiO 2 Inorganic materials 0.000 description 2
- 239000000919 ceramic Substances 0.000 description 2
- BGTFCAQCKWKTRL-YDEUACAXSA-N chembl1095986 Chemical compound C1[C@@H](N)[C@@H](O)[C@H](C)O[C@H]1O[C@@H]([C@H]1C(N[C@H](C2=CC(O)=CC(O[C@@H]3[C@H]([C@@H](O)[C@H](O)[C@@H](CO)O3)O)=C2C=2C(O)=CC=C(C=2)[C@@H](NC(=O)[C@@H]2NC(=O)[C@@H]3C=4C=C(C(=C(O)C=4)C)OC=4C(O)=CC=C(C=4)[C@@H](N)C(=O)N[C@@H](C(=O)N3)[C@H](O)C=3C=CC(O4)=CC=3)C(=O)N1)C(O)=O)=O)C(C=C1)=CC=C1OC1=C(O[C@@H]3[C@H]([C@H](O)[C@@H](O)[C@H](CO[C@@H]5[C@H]([C@@H](O)[C@H](O)[C@@H](C)O5)O)O3)O[C@@H]3[C@H]([C@@H](O)[C@H](O)[C@@H](CO)O3)O[C@@H]3[C@H]([C@H](O)[C@@H](CO)O3)O)C4=CC2=C1 BGTFCAQCKWKTRL-YDEUACAXSA-N 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 229940114081 cinnamate Drugs 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000001723 curing Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000013007 heat curing Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 238000000206 photolithography Methods 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- 150000004756 silanes Chemical class 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 150000003609 titanium compounds Chemical class 0.000 description 2
- WBYWAXJHAXSJNI-VOTSOKGWSA-M trans-cinnamate Chemical compound [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 2
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 1
- KETQAJRQOHHATG-UHFFFAOYSA-N 1,2-naphthoquinone Chemical compound C1=CC=C2C(=O)C(=O)C=CC2=C1 KETQAJRQOHHATG-UHFFFAOYSA-N 0.000 description 1
- HCPAOTGVQASBMP-UHFFFAOYSA-N 2-(oxiran-2-ylmethyl)oxirane Chemical compound C1OC1CC1CO1 HCPAOTGVQASBMP-UHFFFAOYSA-N 0.000 description 1
- WTQZSMDDRMKJRI-UHFFFAOYSA-N 4-diazoniophenolate Chemical compound [O-]C1=CC=C([N+]#N)C=C1 WTQZSMDDRMKJRI-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- DQFBYFPFKXHELB-UHFFFAOYSA-N Chalcone Natural products C=1C=CC=CC=1C(=O)C=CC1=CC=CC=C1 DQFBYFPFKXHELB-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 229910000792 Monel Inorganic materials 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 238000004026 adhesive bonding Methods 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 235000005513 chalcones Nutrition 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000002788 crimping Methods 0.000 description 1
- FHIVAFMUCKRCQO-UHFFFAOYSA-N diazinon Chemical compound CCOP(=S)(OCC)OC1=CC(C)=NC(C(C)C)=N1 FHIVAFMUCKRCQO-UHFFFAOYSA-N 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- CMMUKUYEPRGBFB-UHFFFAOYSA-L dichromic acid Chemical compound O[Cr](=O)(=O)O[Cr](O)(=O)=O CMMUKUYEPRGBFB-UHFFFAOYSA-L 0.000 description 1
- QDWLLVUFTWGZRZ-UHFFFAOYSA-N diphenylmethanone;prop-2-enamide Chemical compound NC(=O)C=C.C=1C=CC=CC=1C(=O)C1=CC=CC=C1 QDWLLVUFTWGZRZ-UHFFFAOYSA-N 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 229920006332 epoxy adhesive Polymers 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- QRWZCJXEAOZAAW-UHFFFAOYSA-N n,n,2-trimethylprop-2-enamide Chemical compound CN(C)C(=O)C(C)=C QRWZCJXEAOZAAW-UHFFFAOYSA-N 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- 239000010680 novolac-type phenolic resin Substances 0.000 description 1
- KQJBQMSCFSJABN-UHFFFAOYSA-N octadecan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCCCCCCCCCCCCCCCC[O-].CCCCCCCCCCCCCCCCCC[O-].CCCCCCCCCCCCCCCCCC[O-].CCCCCCCCCCCCCCCCCC[O-] KQJBQMSCFSJABN-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Substances [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229910000679 solder Inorganic materials 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 229920006305 unsaturated polyester Polymers 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 150000003752 zinc compounds Chemical class 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41J—TYPEWRITERS; SELECTIVE PRINTING MECHANISMS, i.e. MECHANISMS PRINTING OTHERWISE THAN FROM A FORME; CORRECTION OF TYPOGRAPHICAL ERRORS
- B41J2/00—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed
- B41J2/005—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed characterised by bringing liquid or particles selectively into contact with a printing material
- B41J2/01—Ink jet
- B41J2/135—Nozzles
- B41J2/16—Production of nozzles
- B41J2/1621—Manufacturing processes
- B41J2/164—Manufacturing processes thin film formation
- B41J2/1646—Manufacturing processes thin film formation thin film formation by sputtering
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41J—TYPEWRITERS; SELECTIVE PRINTING MECHANISMS, i.e. MECHANISMS PRINTING OTHERWISE THAN FROM A FORME; CORRECTION OF TYPOGRAPHICAL ERRORS
- B41J2/00—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed
- B41J2/005—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed characterised by bringing liquid or particles selectively into contact with a printing material
- B41J2/01—Ink jet
- B41J2/135—Nozzles
- B41J2/16—Production of nozzles
- B41J2/1601—Production of bubble jet print heads
- B41J2/1604—Production of bubble jet print heads of the edge shooter type
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41J—TYPEWRITERS; SELECTIVE PRINTING MECHANISMS, i.e. MECHANISMS PRINTING OTHERWISE THAN FROM A FORME; CORRECTION OF TYPOGRAPHICAL ERRORS
- B41J2/00—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed
- B41J2/005—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed characterised by bringing liquid or particles selectively into contact with a printing material
- B41J2/01—Ink jet
- B41J2/135—Nozzles
- B41J2/16—Production of nozzles
- B41J2/1621—Manufacturing processes
- B41J2/1623—Manufacturing processes bonding and adhesion
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41J—TYPEWRITERS; SELECTIVE PRINTING MECHANISMS, i.e. MECHANISMS PRINTING OTHERWISE THAN FROM A FORME; CORRECTION OF TYPOGRAPHICAL ERRORS
- B41J2/00—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed
- B41J2/005—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed characterised by bringing liquid or particles selectively into contact with a printing material
- B41J2/01—Ink jet
- B41J2/135—Nozzles
- B41J2/16—Production of nozzles
- B41J2/1621—Manufacturing processes
- B41J2/1631—Manufacturing processes photolithography
Landscapes
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Particle Formation And Scattering Control In Inkjet Printers (AREA)
Description
本発明は、インクジエツト記録ヘツド、詳しく
は、所謂インクジエツト記録方式に用いる記録用
インク小滴を発生するためのインクジエツト記録
ヘツドに関する。
インクジエツト記録方式に適用されるインクジ
エツト記録ヘツドは、一般に、微細なインク吐出
口(オリフイス)、インク通路及びこのインク通
路の一部に設けられるインク吐出圧発生部を備え
ている。
従来、この様なインクジエツト記録ヘツドを作
成する方法として、例えば、ガラスや金属の板に
切削やエツチング等により、微細な溝を形成した
後、この溝を形成した板を他の適当な板と接合し
てインク通路の形成を行なう方法が知られてい
る。
しかし、斯かる従来法によつて作成されるヘツ
ドでは、切削加工されるインク通路内壁面の荒れ
が大き過ぎたり、エツチング率の差からインク通
路に歪が生じたりして、精度の良いインク通路が
得難く、製作後のインクジエツト記録ヘツドのイ
ンク吐出特性にバラツキが出易い。また、切削加
工の際に、板の欠けや割れが生じ易く、製造歩留
りが悪いと言う問題点もある。そして、エツチン
グ加工を行なう場合は、製造工程が多く、製造コ
ストの上昇を招くという問題点がある。更に、上
記した従来法に共通する問題点としては、インク
通路溝を形成した溝付板と、インクに作用するエ
ネルギーを発生する圧電素子、発熱素子等の駆動
素子が設けられた蓋板との貼合せの際に、夫々の
位置合せを精度良く行うことが困難であつて量産
性に欠ける点が挙げられる。
これ等の問題点が解決される構成を有するイン
クジエツト記録ヘツドとして、インク吐出圧発生
素子の設置してある基板に感光性樹脂の硬化膜か
らなるインク通路壁を形成し、その後前記通路に
覆いを設けるインクジエツト記録ヘツドが、例え
ば特開昭57−43876号により知られている。
この感光性樹脂を利用して製作されるインクジ
エツト記録ヘツドは、従来のヘツドの問題点であ
つたインク通路の仕上り精度、製造工程の複雑
さ、製造歩留りが悪いという問題点を解決した点
では優れたものである。しかしながら、インク吐
出圧発生素子の設置してある基板と、その上に形
成した感光性樹脂の硬化膜の通路壁の接合力の点
で問題を残していた。いいかえれば、基板に対す
る感光性樹脂硬化膜の密着性が充分でなく、長時
間に亘つてインク滴を吐出させると、インク滴の
吐出の際の衝撃によつて、或いは自身の経時変化
によつて、インク吐出口部分の基板と通路壁が非
常に僅かではあるが剥離し、インク滴の直進性、
すなわちインク着弾点精度に影響を与えている。
このことは、近年インクジエツト記録方式が高密
度ノズルによつて高解像度の画質への要求が高ま
つている中で、大きな障害となつていた。
本発明は、上記の問題点を鑑み成れたもので、
精密であり、信頼性が高く、使用耐久性に優れ
た、高密度高品質な画質を得るためのインクジエ
ツト記録ヘツドを提供することを目的としてい
る。
このような諸目的を達成する本発明のインクジ
エツト記録ヘツドは、感光性樹脂を用いて形成さ
れた膜を利用して、インクが吐出される吐出口に
連通するインク通路が基板上に設けられているイ
ンクジエツト記録ヘツドにおいて、吐出口近傍の
基板上に、無機酸化物及び無機窒化物の少なくと
もいずれか一方からなる帯状の層と、接着向上剤
層と、前記膜と、を順に有していることを特徴と
する。
以下、図面に基づいて本発明を詳細に説明す
る。
先ず、第1図−a乃至第7図−cに示した作成
工程に従つて本発明の実施例を説明する。
第1図−aの工程では、ガラス、セラミツク、
プラスチツク、金属等からなる基板1上に、イン
ク通路に対応して、インクの吐出口からインクを
吐出するために利用されるエネルギーを発生する
エネルギー発生素子2として熱エネルギーを発生
する発熱素子やピエゾ素子等を所望の個数配置す
る。次いで電気絶縁性を付与する目的で、SiO2、
Ta2O5、Al2O3、ガラス、Si3N4、BN等の無機酸
化物、無機窒化物を被覆し、更に耐インク性を与
えるためAu、Pd、Pt等の貴金属、Ti、Cr、Ni、
Ta、Mo、W、Nb等耐食金属又はSUS、モネル
メタル等の耐食合金を保護層として被覆する。な
お、これら保護層は図示されておらず、また、イ
ンク吐出圧発生素子2には信号入力用電極が接続
してある。第1図−bは前記基板の断面図であ
る。
続く第1図−cの工程では、上記インク吐出圧
発生素子2を有する基板表面に無機酸化物及び/
又は無機窒化物3として、蒸着、スパツタリング
等によつてSiO2、Ta2O5、Al2O3、Si3N4、BN、
ガラス等の薄膜を形成する。この場合の無機酸化
物及び/又は無機窒化物の層の厚さとしては、後
で感光性樹脂膜を被覆する際に障害とならないよ
うに5μm以下が好ましい。
第1図−dの工程では、吐出圧発生素子の配置
された基板1のインク吐出口が形成される端面に
臨む部分にだけ前記無機酸化物及び/又は無機窒
化物3が残るように、公知のフオトリソグラフイ
法によつてフオトレジスト像でカバーし、その後
周知の方法で無機酸化物及び/又は無機窒化物3
の不要な部分をエツチングによつて除去する。
但し、上記の方法によらず、すなわち基板1の
表面に新たに無機酸化物及び/又は無機窒化物3
の薄層を被覆することなく、あらかじめ基板1の
耐インク性を高める目的で被覆してある金属薄層
を必要な領域だけフオトリソグラフイー法によつ
て除去し、前記金属薄層の下層にある無機酸化物
及び/又は無機窒化物の層を露出させる方法もあ
る。以上の工程を経て得られたものが図2図−
a、その断面図が第2図−bである。
無機酸化物及び/又は無機窒化物の層3は、第
2図−aに示されたように、特に大きな接着力が
要求されるインク吐出口が形成される基板の端面
に臨む部分に帯状に設けることが好ましいが、イ
ンク通路が形成される部分にはこの層は必要がな
いのでくし状に無機酸化物及び/又は無機窒化物
の層を設けることもできる。
ただし、無機酸化物や無機窒化物を帯状に設け
た場合には、吐出口近傍の基板面上を一様に平坦
にすることができ、更に基板側と感光性樹脂によ
る膜との接着力を向上させることができる。
次に第2図の工程で得られた基板1の表面を浄
化し、80〜110℃で10分間又はそれ以上乾燥させ
た後、接着向上剤(γ−アミノプロピルトリエト
キシシラン、分子構造式NH2(CH2)3Si(OC2H5)3
のエチルアルコール1%溶液)を1000〜6000rpm
でスピンナーコートし、その後80℃で10〜20分間
加熱する。
本発明方法においては、接着向上剤として上記
のγ−アミノプロピルトリエトキシシラン以外
に、一般知られている有機シラン化合物あるいは
有機チタン化合物、有機アルミニウム化合物、有
機亜鉛化合物を使用することができる。これら接
着剤は、使用する感光性樹脂の組成に応じ、感光
性樹脂と反応する官能基を有する接着向上剤を選
択して使用することが好ましい。これら有機シラ
ン化合物及び有機チタン化合物の代表的なものを
官能基別にまとめたのが表1及び表2である。
The present invention relates to an inkjet recording head, and more particularly to an inkjet recording head for generating recording ink droplets used in so-called inkjet recording systems. An inkjet recording head applied to an inkjet recording system generally includes a fine ink ejection opening (orifice), an ink passage, and an ink ejection pressure generating section provided in a part of the ink passage. Conventionally, such an inkjet recording head has been manufactured by forming fine grooves on a glass or metal plate by cutting or etching, and then bonding the plate with the grooves to another suitable plate. There is a known method for forming ink passages. However, in heads manufactured by such conventional methods, the roughness of the inner wall surface of the ink passages to be cut is too large, and distortion occurs in the ink passages due to differences in etching rate. It is difficult to obtain the desired characteristics, and variations tend to occur in the ink ejection characteristics of the inkjet recording head after manufacture. Further, there is also the problem that the plate is likely to chip or crack during cutting, resulting in poor manufacturing yield. When etching is performed, there are many manufacturing steps, which leads to an increase in manufacturing costs. Furthermore, a problem common to the above-mentioned conventional methods is that the grooved plate in which the ink passage grooves are formed and the lid plate provided with drive elements such as piezoelectric elements and heating elements that generate energy that acts on the ink. During lamination, it is difficult to align the respective positions with high precision, and mass production is lacking. An inkjet recording head having a configuration that solves these problems involves forming an ink passage wall made of a cured film of a photosensitive resin on a substrate on which an ink ejection pressure generating element is installed, and then covering the passage. An inkjet recording head is known, for example, from JP-A-57-43876. The inkjet recording head manufactured using this photosensitive resin is superior in that it solves the problems of conventional heads, such as the precision of the ink passage finish, the complexity of the manufacturing process, and poor manufacturing yield. It is something that However, there remains a problem in the bonding strength between the substrate on which the ink ejection pressure generating element is installed and the passage wall of the cured photosensitive resin film formed thereon. In other words, if the adhesiveness of the photosensitive resin cured film to the substrate is not sufficient and ink droplets are ejected for a long time, the ink droplets may be damaged due to the impact during ejection or due to changes over time. , the substrate at the ink ejection port and the passage wall peeled off, albeit very slightly, and the straightness of the ink droplets deteriorated.
In other words, it affects the accuracy of the ink landing point.
This has become a major hindrance in recent years as the demand for high-resolution image quality in inkjet recording systems has increased due to the use of high-density nozzles. The present invention was made in view of the above problems.
The object of the present invention is to provide an inkjet recording head that is precise, highly reliable, and has excellent durability in use, and is capable of producing high-density, high-quality images. The inkjet recording head of the present invention, which achieves these objects, has an ink passage formed on a substrate that communicates with an ejection port through which ink is ejected, using a film formed using a photosensitive resin. In the inkjet recording head, the substrate near the ejection port has, in this order, a band-shaped layer made of at least one of an inorganic oxide and an inorganic nitride, an adhesion improver layer, and the above film. It is characterized by Hereinafter, the present invention will be explained in detail based on the drawings. First, an embodiment of the present invention will be described according to the manufacturing steps shown in FIGS. 1-a to 7-c. In the process shown in Figure 1-a, glass, ceramic,
On a substrate 1 made of plastic, metal, etc., a heating element or piezoelectric element that generates thermal energy is installed as an energy generating element 2 that generates energy used to eject ink from an ink ejection port, corresponding to an ink passage. A desired number of elements etc. are arranged. Next, for the purpose of imparting electrical insulation, SiO 2 ,
Coated with inorganic oxides and inorganic nitrides such as Ta 2 O 5 , Al 2 O 3 , glass, Si 3 N 4 and BN, and noble metals such as Au, Pd and Pt, Ti and Cr to provide further ink resistance. ,Ni,
A corrosion-resistant metal such as Ta, Mo, W, or Nb or a corrosion-resistant alloy such as SUS or Monel metal is coated as a protective layer. Note that these protective layers are not shown, and a signal input electrode is connected to the ink ejection pressure generating element 2. FIG. 1-b is a sectional view of the substrate. In the subsequent step of FIG. 1-c, inorganic oxide and/or inorganic oxide and/or
Or, as the inorganic nitride 3, SiO 2 , Ta 2 O 5 , Al 2 O 3 , Si 3 N 4 , BN,
Forms a thin film of glass, etc. In this case, the thickness of the inorganic oxide and/or inorganic nitride layer is preferably 5 .mu.m or less so as not to become a hindrance during later coating with a photosensitive resin film. In the step of FIG. 1-d, the inorganic oxide and/or inorganic nitride 3 is left only on the portion facing the end face where the ink ejection port is formed of the substrate 1 on which the ejection pressure generating element is arranged. covered with a photoresist image by the photolithographic method of
Remove unnecessary parts by etching. However, if the method described above is not used, in other words, the inorganic oxide and/or inorganic nitride 3 is newly added to the surface of the substrate 1.
The thin metal layer that has been coated in advance to improve the ink resistance of the substrate 1 is removed by photolithography only in the necessary areas, without coating the thin metal layer below the thin metal layer. Another method is to expose a layer of inorganic oxide and/or inorganic nitride. Figure 2 shows what was obtained through the above steps.
a, and its cross-sectional view is shown in FIG. 2-b. As shown in FIG. 2-a, the inorganic oxide and/or inorganic nitride layer 3 is formed in a band-like manner on the part facing the end surface of the substrate where the ink ejection openings, which require particularly high adhesive strength, are formed. Although it is preferable to provide this layer, since this layer is not necessary in the portion where the ink passage is formed, a comb-shaped layer of inorganic oxide and/or inorganic nitride may also be provided. However, if an inorganic oxide or inorganic nitride is provided in a band shape, the surface of the substrate near the discharge port can be made uniformly flat, and the adhesive force between the substrate side and the film made of photosensitive resin can be improved. can be improved. Next, the surface of the substrate 1 obtained in the process shown in Fig. 2 is cleaned and dried at 80 to 110°C for 10 minutes or more. 2 (CH 2 ) 3 Si (OC 2 H 5 ) 3
(1% solution of ethyl alcohol) at 1000 to 6000 rpm
Coat with a spinner and then heat at 80°C for 10-20 minutes. In the method of the present invention, in addition to the above-mentioned γ-aminopropyltriethoxysilane, generally known organic silane compounds, organic titanium compounds, organic aluminum compounds, and organic zinc compounds can be used as adhesion improvers. For these adhesives, it is preferable to select and use an adhesion improver having a functional group that reacts with the photosensitive resin, depending on the composition of the photosensitive resin used. Tables 1 and 2 summarize typical organic silane compounds and organic titanium compounds by functional group.
【表】【table】
【表】【table】
【表】【table】
【表】【table】
【表】
第3図の工程では、第2図の工程を経て得られ
た基板1の表面を浄化し、乾燥させた後、その表
面に80℃〜105℃程度に加温された感光性樹脂で
あるドライフイルムフオトレジスト5(膜厚、約
25μm〜100μm)を0.5〜4f/分の速度、1〜3
Kg/cm2の加圧条件下でラミネートする。このと
き、ドライフイルムフオトレジスト5は自己接着
性を示して基板1の表面に融着して固定され、以
後、相当の外圧が加わつた場合にも基板1から剥
離することはない。特に、本実施例では発熱素子
や電極等や形成するのと同様な半導体製造工程を
用いて無機酸化物や無機窒化物を基板上に設けて
いるが、この無機酸化物や無機窒化物の層と基板
側とは密着力が大であると共に、また接着向上剤
との分子的レベルでの結合(化学的な結合力によ
る結合)が良いため、結果としてドライフイルム
フオトレジスト5との密着が強固に行われる。
続いて、第4図に示す様に、基板面に設けたド
ライフイルムフオトレジスト5上に所定のパター
ンを有するフオトマスク6を重ね合せた後、この
フオトマスク6の上部から露光を行う。このと
き、インク吐出圧発生素子2の設置位置と上記パ
ターンの位置合せを公知の手法で行つておく必要
がある。
第5図は、上記露光済みのドライフイルムフオ
トレジスト5の未露光部分を所定の有機溶剤から
成る現像液にて溶解除去した工程を示す説明図で
ある。次に、基板1に残されたドライフイルムフ
オトレジストの露光された部分5pの耐インク性
向上のため、熱硬化処理(例えば150℃〜250℃で
30分〜6時間、加熱)又は、紫外線照射(例えば
50〜200mW/cm2又はそれ以上の紫外線強度で)
を行い、充分に重合硬化反応を進める。上記熱硬
化と紫外線による硬化の両方を兼用するのも効果
的である。
第6図は、上記の充分な重合を終えた硬化した
ドライフイルムレジスト5pでインク通路となる
溝9の形成された基板1に覆いとなる平板8を接
着するか単に圧着して固定したところを示す図で
ある。第6図に示す工程に於て、覆いを付設する
具体的方法としては、
(1) ガラス、セラミツクス、金属、プラスチツク
等の平板8にエポキシ系接着剤を厚さ3〜4μ
mにスピンナーコートした後、予備加熱して接
着剤を所謂、Bステージ化させ、これを硬化し
たフオトレジスト膜5p上に貼り合せて前記接
着剤を本硬化させる。或は、
(2) アクリル系樹脂、ABS樹脂、ポリエチレン
等の熱可塑性樹脂の平板8を硬化したフオトレ
ジスト膜5p上に、直接、熱融着させる方法が
ある。
ここで、第6図示の工程終了後のヘツド外観を
第7図−aに、模式的斜視図で示す。第7図−a
中、9−1はインク供給室、9はインク細流路、
10はインク供給室9−1に不図示のインク供給
管を連結させる為の貫通孔を示している。
このようにして溝を形成した基板と平板との接
合が完了した後、第7図のC−C′線に沿つて切断
する。これは、インク細流路9に於て、インク吐
出圧発生素子2とインク吐出口7との間隔を最適
化する為に行うものであり、ここで切断する領域
は適宜、決定される。この切断に際しては、半導
体工業で通常、採用されているダイシング法が採
用される。
第7図−bは第7図−aのA−A′線切断面図
である。そして、切断面を研磨して平滑化し、貫
通孔10にインク供給管11を取り付けてインク
ジエツト記録ヘツドが完成する。(第7図−c)
以上、図面に基づいて説明した実施例に於て
は、溝作成用の感光性組成物(フオトレジスト)
としてドライフイルムタイプ、つまり固体のもの
を利用したが、本発明では、これのみに限るもの
ではなく、液状の感光性組成物も勿論、利用する
ことができる。基板上へのこの感光性組成物塗膜
の形成方法として、液体の場合にはレリーフ画像
の製作時に用いられるスキージによる方法、すな
わち所望の感光性組成物膜厚に応じた高さの壁を
基板の周囲におき、スキージによつて余分の組成
物を除去する方法である。この場合感光性組成物
の粘度は100cp〜300cpが適当である。また、基
板の周囲におく壁の高さは感光性組成物の溶剤分
の蒸発の減量を見込んで決定する必要がある。
他方、固体の場合は、感光性組成物シートを基
板上に加熱圧着して貼着する。尚、本発明に於て
は、その取扱い上、及び厚さの制御が容易且つ精
確にできる点で、固体のフイルムタイプのものを
利用する方が有利ではある。
このような固体のものとしては、例えば、デユ
ポン社パーマネントフオトポリマーコーテイング
RISTON(ソルダーマスク)730S、同740S、同
730FR、同740FR、同SM1等の商品名で市販され
ている感光性樹脂がある。この他、本発明におい
て使用される感光性組成物としては、感光性樹
脂、フオトレジスト等の通常のフオトリソグラフ
イーの分野において使用されている感光性組成物
の多くのものが挙げられる。これ等の感光性組成
物としては、例えば、ジアゾレジン、P−ジアゾ
キノン、更には例えばビニルモノマーと重合開発
剤を使用する光重合型フオトポリマー、ポリビニ
ルシンナメート等と増感剤を使用する二量化型フ
オトポリマー、オルソナフトキノンジアジドとノ
ボラツクタイプのフエノール樹脂との混合物、ポ
リビニルアルコールとジアゾ樹脂の混合物、4−
グリシジルエチレンオキシドとベンゾフエノンや
グリシジルカルコンとを共重合させたポリエーテ
ル型フオトポリマー、N,N−ジメチルメタクリ
ルアミドと例えばアクリルアミドベンゾフエノン
との共重合体、不飽和ポリエスエル系感光性樹脂
〔例えばAPR(旭化成)、テビスタ(帝人)、ゾン
ネ(関西ペイント)等〕、不飽飽ウレタンオリゴ
マー系感光性樹脂、二官能アクリルモノマーに光
重合開始剤とポリマーとを混合した感光性組成
物、重クロム酸系フオトレジスト、非クロム系水
溶性フオトレジスト、ポリケイ皮酸ビニル系フオ
トレジスト、環化ゴム−アジド系フオトレジス
ト、等が挙げられる。
以上詳しく説明した本発明の効果としては、次
のようなことがあげられる。
1 基板と感光性樹脂の接着が増したことによ
り、特に衝撃のかかるインク吐出口形成の切断
によつても基板からの感光性樹脂の剥れがなく
なつた。
2 接着部の耐溶剤性が向上し、エチレングリコ
ール等の溶剤を含むインクの使用によつても基
板と感光性樹脂硬化膜の通路壁が剥離すること
がなくなつた。
3 インク吐出口の形状安定性が高いため、経時
的なインク着弾点精度が高い。
これら本発明の効果は、以下に示す実施例によ
り、より具体的に説明される。
実施例1〜6及び比較例1〜3
各例間でインク吐出口が形成される端面に臨む
部分の保護層の上に無機酸化物又は無機窒化物の
層を設け又は設けなかつたこと並びにその層を(a)
γ−アミノプロピルエトキシシラン又は(b)テトラ
ステアリルチタネートで処理を実施し又は実施し
なかつたことを除いては、先に示した実施例の工
程(第1図乃至第7図)に従つてインク吐出口を
10個有するインクジエツト記録ヘツドを多数試作
した。これら試作ヘツドのうち、基板と感光性樹
脂の剥離のない正常なものについて、水20%及び
エチレングリコール80%の組成の80℃の溶液に
1000時間の浸漬試験を行つた。これらの結果を表
3に示す。
また、実施例1及び比較例1で得たインクジエ
ツト記録ヘツドに対して、108パルスの耐久印字
試験を行つたところ、実施例のヘツドでは着弾点
精度が±12μm/2mm飛翔距離であつたのに対し
比較例のヘツドでは±60μm/2mm飛翔距離であ
つた。
なお、感光性樹脂は全てRISTON730Sドライ
フイルムフオトレジスト(デユポン社製、商品
名)を使用した。[Table] In the step shown in FIG. 3, the surface of the substrate 1 obtained through the step shown in FIG. Dry film photoresist 5 (film thickness, approx.
25μm~100μm) at a speed of 0.5~4f/min, 1~3
Laminate under pressure conditions of Kg/ cm2 . At this time, the dry film photoresist 5 exhibits self-adhesive properties and is fused and fixed to the surface of the substrate 1, and will not peel off from the substrate 1 even if considerable external pressure is applied thereafter. In particular, in this example, an inorganic oxide or inorganic nitride is provided on the substrate using the same semiconductor manufacturing process as that used to form heating elements, electrodes, etc. It has strong adhesion to the substrate side, and also has good bonding with the adhesion improver at the molecular level (bonding due to chemical bonding force), resulting in strong adhesion to the dry film photoresist 5. It will be held on. Subsequently, as shown in FIG. 4, a photomask 6 having a predetermined pattern is superimposed on the dry film photoresist 5 provided on the substrate surface, and then the photomask 6 is exposed to light from above. At this time, it is necessary to align the installation position of the ink ejection pressure generating element 2 and the pattern using a known method. FIG. 5 is an explanatory diagram showing a process in which the unexposed portions of the exposed dry film photoresist 5 are dissolved and removed using a developer made of a predetermined organic solvent. Next, in order to improve the ink resistance of the exposed portion 5p of the dry film photoresist left on the substrate 1, heat curing treatment (for example, at 150°C to 250°C) is performed.
heating for 30 minutes to 6 hours) or ultraviolet irradiation (e.g.
(with UV intensity of 50-200mW/ cm2 or higher)
to sufficiently advance the polymerization and curing reaction. It is also effective to use both the above-mentioned heat curing and ultraviolet curing. FIG. 6 shows the cured dry film resist 5p that has been sufficiently polymerized as described above, and a flat plate 8 serving as a cover is fixed to the substrate 1 in which grooves 9 serving as ink passages are formed, either by gluing or simply crimping the resist 5p. FIG. In the process shown in Figure 6, the specific method for attaching the cover is as follows: (1) Apply epoxy adhesive to a thickness of 3 to 4 μm on a flat plate 8 made of glass, ceramics, metal, plastic, etc.
After applying spinner coating to the photoresist film 5p, the adhesive is preheated to bring it to the so-called B stage, and this is bonded onto the cured photoresist film 5p to fully cure the adhesive. Alternatively, (2) there is a method of directly heat-sealing a flat plate 8 of thermoplastic resin such as acrylic resin, ABS resin, polyethylene, etc. onto the hardened photoresist film 5p. Here, the appearance of the head after the process shown in FIG. 6 is completed is shown in a schematic perspective view in FIG. 7-a. Figure 7-a
Inside, 9-1 is an ink supply chamber, 9 is an ink narrow flow path,
Reference numeral 10 indicates a through hole for connecting an ink supply pipe (not shown) to the ink supply chamber 9-1. After the substrate in which the grooves have been formed and the flat plate are bonded together in this way, the substrate is cut along line CC' in FIG. This is done to optimize the distance between the ink ejection pressure generating element 2 and the ink ejection opening 7 in the ink narrow flow path 9, and the area to be cut here is determined as appropriate. For this cutting, a dicing method commonly used in the semiconductor industry is used. FIG. 7-b is a cross-sectional view taken along line A-A' in FIG. 7-a. Then, the cut surface is polished to make it smooth, and the ink supply tube 11 is attached to the through hole 10 to complete the inkjet recording head. (Fig. 7-c) In the embodiments described above based on the drawings, the photosensitive composition (photoresist) for creating grooves is
Although a dry film type, that is, a solid composition was used as the composition, the present invention is not limited to this, and of course, a liquid photosensitive composition can also be used. In the case of a liquid, the photosensitive composition coating film is formed on the substrate by using a squeegee, which is used when producing a relief image. In this method, excess composition is removed using a squeegee. In this case, the appropriate viscosity of the photosensitive composition is 100 cp to 300 cp. Further, the height of the wall around the substrate must be determined in consideration of the reduction in evaporation of the solvent component of the photosensitive composition. On the other hand, in the case of a solid, the photosensitive composition sheet is attached to the substrate by heat-pressing. In the present invention, it is advantageous to use a solid film type material in terms of its handling and the fact that the thickness can be easily and precisely controlled. Such solid materials include, for example, DuPont's permanent photopolymer coatings.
RISTON (solder mask) 730S, 740S, RISTON
There are photosensitive resins commercially available under trade names such as 730FR, 740FR, and SM1. In addition, the photosensitive composition used in the present invention includes many photosensitive compositions used in the field of ordinary photolithography, such as photosensitive resins and photoresists. These photosensitive compositions include, for example, diazoresin, P-diazoquinone, photopolymerizable photopolymers using a vinyl monomer and a polymerization developer, and dimerized photopolymers using polyvinyl cinnamate and a sensitizer. Photopolymer, mixture of orthonaphthoquinone diazide and novolac type phenolic resin, mixture of polyvinyl alcohol and diazo resin, 4-
Polyether-type photopolymers made by copolymerizing glycidyl ethylene oxide with benzophenone or glycidyl chalcone, copolymers of N,N-dimethylmethacrylamide with, for example, acrylamide benzophenone, unsaturated polyester-based photosensitive resins [for example, APR (Asahi Kasei Co., Ltd.)] ), Tevista (Teijin), Sonne (Kansai Paint), etc.], unsaturated urethane oligomer-based photosensitive resins, photosensitive compositions in which a difunctional acrylic monomer is mixed with a photopolymerization initiator and a polymer, dichromic acid-based photosensitive resins, etc. resist, non-chromium water-soluble photoresist, polyvinyl cinnamate photoresist, cyclized rubber-azide photoresist, and the like. The effects of the present invention described in detail above include the following. 1. Due to the increased adhesion between the substrate and the photosensitive resin, the photosensitive resin no longer peels off from the substrate even when cutting the ink ejection port formation, which is particularly impactful. 2. The solvent resistance of the bonded portion has been improved, and the passage wall between the substrate and the photosensitive resin cured film no longer peels off even when ink containing a solvent such as ethylene glycol is used. 3. Since the shape stability of the ink ejection port is high, the accuracy of the ink landing point over time is high. These effects of the present invention will be explained more specifically by the examples shown below. Examples 1 to 6 and Comparative Examples 1 to 3 Between each example, an inorganic oxide or inorganic nitride layer was provided or not provided on a portion of the protective layer facing the end face where an ink ejection port is formed, and layer(a)
The inks were prepared according to the steps of the examples set forth above (Figures 1 to 7), with or without treatment with gamma-aminopropylethoxysilane or (b) tetrastearyl titanate. outlet
A number of trial inkjet recording heads with 10 heads were manufactured. Among these prototype heads, normal ones with no peeling between the substrate and the photosensitive resin were soaked in a solution of 20% water and 80% ethylene glycol at 80°C.
A 1000 hour immersion test was conducted. These results are shown in Table 3. Furthermore, when a 10 8 pulse durability printing test was conducted on the inkjet recording heads obtained in Example 1 and Comparative Example 1, the impact point accuracy was ±12 μm/2 mm flight distance in the example head. In contrast, the flight distance of the comparative head was ±60 μm/2 mm. The photosensitive resin used was RISTON730S dry film photoresist (manufactured by DuPont, trade name).
第1図−a乃至第7図−cは本発明のインクジ
エツト記録ヘツドをその製造工程に従つて説明す
るための模式図である。
1:基板、2:インク吐出圧発生素子、3:無
機酸化物及び/又は無機窒化物層、4:フオトレ
ジスト像、5:ドライフイルムフオトレジスト、
6:フオトマスク、7:インク吐出口、8:覆
い、9:インク細流路、9−1:インク供給室、
10:貫通孔、11:インク供給管。
FIGS. 1-a to 7-c are schematic diagrams for explaining the inkjet recording head of the present invention according to its manufacturing process. 1: Substrate, 2: Ink discharge pressure generating element, 3: Inorganic oxide and/or inorganic nitride layer, 4: Photoresist image, 5: Dry film photoresist,
6: Photomask, 7: Ink discharge port, 8: Cover, 9: Ink narrow channel, 9-1: Ink supply chamber,
10: Through hole, 11: Ink supply pipe.
Claims (1)
て、インクが吐出される吐出口に連通するインク
通路が基板上に設けられているインクジエツト記
録ヘツドにおいて、 前記吐出口近傍の前記基板上に、無機酸化物及
び無機窒化物の少なくともいずれか一方からなる
帯状の層と、接着向上剤層と、前記膜と、を順に
有していることを特徴とするインクジエツト記録
ヘツド。 2 前記インク通路に対応して、前記吐出口から
インクを吐出するために利用されるエネルギーを
発生するエネルギー発生素子が設けられているこ
とを特徴とする特許請求の範囲第1項に記載のイ
ンクジエツト記録ヘツド。 3 前記エネルギー発生素子は、前記エネルギー
として熱エネルギーを発生する素子である特許請
求の範囲第2項に記載のインクジエツト記録ヘツ
ド。 4 前記エネルギー発生素子はピエゾ素子である
特許請求の範囲第2項に記載のインクジエツト記
録ヘツド。[Scope of Claims] 1. An inkjet recording head in which an ink passage communicating with an ejection port through which ink is ejected is provided on a substrate using a film formed using a photosensitive resin, the ejection port comprising: An inkjet recording head characterized in that it has a strip-shaped layer made of at least one of an inorganic oxide and an inorganic nitride, an adhesion improver layer, and the film on the substrate nearby, in this order. . 2. The ink jet according to claim 1, wherein an energy generating element that generates energy used for ejecting ink from the ejection port is provided corresponding to the ink passage. Record head. 3. The inkjet recording head according to claim 2, wherein the energy generating element is an element that generates thermal energy as the energy. 4. The inkjet recording head according to claim 2, wherein the energy generating element is a piezo element.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10944782A JPS58224758A (en) | 1982-06-25 | 1982-06-25 | inkjet recording head |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10944782A JPS58224758A (en) | 1982-06-25 | 1982-06-25 | inkjet recording head |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS58224758A JPS58224758A (en) | 1983-12-27 |
| JPH0415096B2 true JPH0415096B2 (en) | 1992-03-16 |
Family
ID=14510465
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP10944782A Granted JPS58224758A (en) | 1982-06-25 | 1982-06-25 | inkjet recording head |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS58224758A (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH064323B2 (en) * | 1984-05-08 | 1994-01-19 | キヤノン株式会社 | Liquid jet recording head |
| JP3115720B2 (en) * | 1992-09-29 | 2000-12-11 | キヤノン株式会社 | INK JET PRINT HEAD, INK JET PRINTING APPARATUS HAVING THE PRINT HEAD, AND METHOD OF MANUFACTURING THE PRINT HEAD |
| JP4669138B2 (en) * | 2001-02-22 | 2011-04-13 | キヤノン株式会社 | Method for manufacturing ink jet recording head |
| US12600130B2 (en) | 2023-08-22 | 2026-04-14 | Brady Worldwide, Inc. | Ejection head nozzle flooding control |
-
1982
- 1982-06-25 JP JP10944782A patent/JPS58224758A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS58224758A (en) | 1983-12-27 |
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