JPWO2006068000A1 - COF substrate laminate, method for producing the same, and COF film carrier tape formed using this COF substrate laminate - Google Patents
COF substrate laminate, method for producing the same, and COF film carrier tape formed using this COF substrate laminate Download PDFInfo
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- JPWO2006068000A1 JPWO2006068000A1 JP2006548842A JP2006548842A JPWO2006068000A1 JP WO2006068000 A1 JPWO2006068000 A1 JP WO2006068000A1 JP 2006548842 A JP2006548842 A JP 2006548842A JP 2006548842 A JP2006548842 A JP 2006548842A JP WO2006068000 A1 JPWO2006068000 A1 JP WO2006068000A1
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- 239000000758 substrate Substances 0.000 title claims abstract description 29
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 10
- 239000004020 conductor Substances 0.000 claims abstract description 55
- 230000003746 surface roughness Effects 0.000 claims abstract description 41
- 239000011888 foil Substances 0.000 claims abstract description 22
- 239000002184 metal Substances 0.000 claims abstract description 19
- 229910052751 metal Inorganic materials 0.000 claims abstract description 19
- 239000011347 resin Substances 0.000 claims abstract description 16
- 229920005989 resin Polymers 0.000 claims abstract description 16
- 229920001721 polyimide Polymers 0.000 claims description 25
- 238000005498 polishing Methods 0.000 claims description 19
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- 238000001035 drying Methods 0.000 claims description 8
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- 239000010410 layer Substances 0.000 description 82
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 54
- 239000011889 copper foil Substances 0.000 description 51
- 238000006243 chemical reaction Methods 0.000 description 15
- 239000009719 polyimide resin Substances 0.000 description 15
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 12
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- 238000003786 synthesis reaction Methods 0.000 description 8
- 150000008065 acid anhydrides Chemical class 0.000 description 7
- 150000004985 diamines Chemical class 0.000 description 7
- HLBLWEWZXPIGSM-UHFFFAOYSA-N 4-Aminophenyl ether Chemical compound C1=CC(N)=CC=C1OC1=CC=C(N)C=C1 HLBLWEWZXPIGSM-UHFFFAOYSA-N 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- ANSXAPJVJOKRDJ-UHFFFAOYSA-N furo[3,4-f][2]benzofuran-1,3,5,7-tetrone Chemical compound C1=C2C(=O)OC(=O)C2=CC2=C1C(=O)OC2=O ANSXAPJVJOKRDJ-UHFFFAOYSA-N 0.000 description 6
- 239000005457 ice water Substances 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 4
- 238000009413 insulation Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- ZHBXLZQQVCDGPA-UHFFFAOYSA-N 5-[(1,3-dioxo-2-benzofuran-5-yl)sulfonyl]-2-benzofuran-1,3-dione Chemical compound C1=C2C(=O)OC(=O)C2=CC(S(=O)(=O)C=2C=C3C(=O)OC(C3=CC=2)=O)=C1 ZHBXLZQQVCDGPA-UHFFFAOYSA-N 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- 238000002788 crimping Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 229920006259 thermoplastic polyimide Polymers 0.000 description 3
- XFDUHJPVQKIXHO-UHFFFAOYSA-N 3-aminobenzoic acid Chemical compound NC1=CC=CC(C(O)=O)=C1 XFDUHJPVQKIXHO-UHFFFAOYSA-N 0.000 description 2
- WUPRYUDHUFLKFL-UHFFFAOYSA-N 4-[3-(4-aminophenoxy)phenoxy]aniline Chemical compound C1=CC(N)=CC=C1OC1=CC=CC(OC=2C=CC(N)=CC=2)=C1 WUPRYUDHUFLKFL-UHFFFAOYSA-N 0.000 description 2
- ZNVDOKOOMPHOSP-UHFFFAOYSA-N 4-amino-n-(4-amino-2-methoxyphenyl)benzamide Chemical compound COC1=CC(N)=CC=C1NC(=O)C1=CC=C(N)C=C1 ZNVDOKOOMPHOSP-UHFFFAOYSA-N 0.000 description 2
- 241000989747 Maba Species 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- WKDNYTOXBCRNPV-UHFFFAOYSA-N bpda Chemical compound C1=C2C(=O)OC(=O)C2=CC(C=2C=C3C(=O)OC(C3=CC=2)=O)=C1 WKDNYTOXBCRNPV-UHFFFAOYSA-N 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 2
- 229910052737 gold Inorganic materials 0.000 description 2
- 239000010931 gold Substances 0.000 description 2
- 238000007731 hot pressing Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- IXHBSOXJLNEOPY-UHFFFAOYSA-N 2'-anilino-6'-(n-ethyl-4-methylanilino)-3'-methylspiro[2-benzofuran-3,9'-xanthene]-1-one Chemical compound C=1C=C(C2(C3=CC=CC=C3C(=O)O2)C2=CC(NC=3C=CC=CC=3)=C(C)C=C2O2)C2=CC=1N(CC)C1=CC=C(C)C=C1 IXHBSOXJLNEOPY-UHFFFAOYSA-N 0.000 description 1
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 1
- ZGDMDBHLKNQPSD-UHFFFAOYSA-N 2-amino-5-(4-amino-3-hydroxyphenyl)phenol Chemical group C1=C(O)C(N)=CC=C1C1=CC=C(N)C(O)=C1 ZGDMDBHLKNQPSD-UHFFFAOYSA-N 0.000 description 1
- QYIMZXITLDTULQ-UHFFFAOYSA-N 4-(4-amino-2-methylphenyl)-3-methylaniline Chemical group CC1=CC(N)=CC=C1C1=CC=C(N)C=C1C QYIMZXITLDTULQ-UHFFFAOYSA-N 0.000 description 1
- KHYXYOGWAIYVBD-UHFFFAOYSA-N 4-(4-propylphenoxy)aniline Chemical compound C1=CC(CCC)=CC=C1OC1=CC=C(N)C=C1 KHYXYOGWAIYVBD-UHFFFAOYSA-N 0.000 description 1
- JCRRFJIVUPSNTA-UHFFFAOYSA-N 4-[4-(4-aminophenoxy)phenoxy]aniline Chemical compound C1=CC(N)=CC=C1OC(C=C1)=CC=C1OC1=CC=C(N)C=C1 JCRRFJIVUPSNTA-UHFFFAOYSA-N 0.000 description 1
- XPAQFJJCWGSXGJ-UHFFFAOYSA-N 4-amino-n-(4-aminophenyl)benzamide Chemical compound C1=CC(N)=CC=C1NC(=O)C1=CC=C(N)C=C1 XPAQFJJCWGSXGJ-UHFFFAOYSA-N 0.000 description 1
- QQGYZOYWNCKGEK-UHFFFAOYSA-N 5-[(1,3-dioxo-2-benzofuran-5-yl)oxy]-2-benzofuran-1,3-dione Chemical compound C1=C2C(=O)OC(=O)C2=CC(OC=2C=C3C(=O)OC(C3=CC=2)=O)=C1 QQGYZOYWNCKGEK-UHFFFAOYSA-N 0.000 description 1
- 229910000881 Cu alloy Inorganic materials 0.000 description 1
- 229910016847 F2-WS Inorganic materials 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- GTDPSWPPOUPBNX-UHFFFAOYSA-N ac1mqpva Chemical compound CC12C(=O)OC(=O)C1(C)C1(C)C2(C)C(=O)OC1=O GTDPSWPPOUPBNX-UHFFFAOYSA-N 0.000 description 1
- -1 and then Substances 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N ethyl acetate Substances CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 238000000059 patterning Methods 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 238000007517 polishing process Methods 0.000 description 1
- 229920003223 poly(pyromellitimide-1,4-diphenyl ether) Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L23/00—Details of semiconductor or other solid state devices
- H01L23/48—Arrangements for conducting electric current to or from the solid state body in operation, e.g. leads, terminal arrangements ; Selection of materials therefor
- H01L23/488—Arrangements for conducting electric current to or from the solid state body in operation, e.g. leads, terminal arrangements ; Selection of materials therefor consisting of soldered or bonded constructions
- H01L23/498—Leads, i.e. metallisations or lead-frames on insulating substrates, e.g. chip carriers
- H01L23/4985—Flexible insulating substrates
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/48—Manufacture or treatment of parts, e.g. containers, prior to assembly of the devices, using processes not provided for in a single one of the subgroups H01L21/06 - H01L21/326
- H01L21/4814—Conductive parts
- H01L21/4846—Leads on or in insulating or insulated substrates, e.g. metallisation
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K3/00—Apparatus or processes for manufacturing printed circuits
- H05K3/0011—Working of insulating substrates or insulating layers
- H05K3/0017—Etching of the substrate by chemical or physical means
- H05K3/002—Etching of the substrate by chemical or physical means by liquid chemical etching
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2924/00—Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
- H01L2924/0001—Technical content checked by a classifier
- H01L2924/0002—Not covered by any one of groups H01L24/00, H01L24/00 and H01L2224/00
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K1/00—Printed circuits
- H05K1/02—Details
- H05K1/0266—Marks, test patterns or identification means
- H05K1/0269—Marks, test patterns or identification means for visual or optical inspection
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K1/00—Printed circuits
- H05K1/02—Details
- H05K1/03—Use of materials for the substrate
- H05K1/0393—Flexible materials
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K2201/00—Indexing scheme relating to printed circuits covered by H05K1/00
- H05K2201/01—Dielectrics
- H05K2201/0104—Properties and characteristics in general
- H05K2201/0108—Transparent
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K2201/00—Indexing scheme relating to printed circuits covered by H05K1/00
- H05K2201/01—Dielectrics
- H05K2201/0183—Dielectric layers
- H05K2201/0191—Dielectric layers wherein the thickness of the dielectric plays an important role
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K2201/00—Indexing scheme relating to printed circuits covered by H05K1/00
- H05K2201/03—Conductive materials
- H05K2201/0332—Structure of the conductor
- H05K2201/0335—Layered conductors or foils
- H05K2201/0355—Metal foils
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K2203/00—Indexing scheme relating to apparatus or processes for manufacturing printed circuits covered by H05K3/00
- H05K2203/07—Treatments involving liquids, e.g. plating, rinsing
- H05K2203/0756—Uses of liquids, e.g. rinsing, coating, dissolving
- H05K2203/0759—Forming a polymer layer by liquid coating, e.g. a non-metallic protective coating or an organic bonding layer
Landscapes
- Engineering & Computer Science (AREA)
- Microelectronics & Electronic Packaging (AREA)
- General Physics & Mathematics (AREA)
- Computer Hardware Design (AREA)
- Manufacturing & Machinery (AREA)
- Power Engineering (AREA)
- Physics & Mathematics (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Ceramic Engineering (AREA)
- Laminated Bodies (AREA)
- Manufacturing Of Printed Wiring (AREA)
- Wire Bonding (AREA)
- Parts Printed On Printed Circuit Boards (AREA)
Abstract
絶縁層を透過してドライバICチップの配線を認識することが可能であると共に、導体と絶縁層との間の接着力が高く、耐エレクトロマイグレーション性に優れ、例えば30μmピッチ以下の微細加工可能な積層体とその製造方法を提供する。導電性金属箔よりなる導体の一方の面に絶縁性樹脂よりなる絶縁層が形成されたCOF基板用積層体であり、導体の厚みが1〜8μmであり、導体の絶縁層と接している面の表面粗さRzが1.0μm以下であり、かつ、導体の絶縁層と接していない面の表面粗さRzが1 .0μm以下であるCOF基板用積層体であり、また、少なくとも10μm以上の厚みを有し、かつ、一方の面の表面粗さRzが1.0μm以下である導電性金属箔の当該面に絶縁層を形成し、この絶縁層と接していない導電性金属箔の面を化学研摩しこの導電性金属箔の厚みを1〜8μmにすると共に、表面粗さRzを1.0μm以下にして導体を形成するCOF基板用積層体の製造方法である。It is possible to recognize the wiring of the driver IC chip through the insulating layer, and has a high adhesive force between the conductor and the insulating layer, and is excellent in electromigration resistance. For example, it can be finely processed with a pitch of 30 μm or less. A laminate and a method for manufacturing the same are provided. COF substrate laminate in which an insulating layer made of an insulating resin is formed on one side of a conductor made of conductive metal foil, the thickness of the conductor being 1-8 μm, and the surface in contact with the insulating layer of the conductor COF substrate laminate having a surface roughness Rz of 1.0 μm or less and a surface roughness Rz of the surface not contacting the conductor insulating layer of 1.0 μm or less, and a thickness of at least 10 μm or more An insulating layer is formed on the surface of the conductive metal foil having a surface roughness Rz of 1.0 μm or less on one surface, and the surface of the conductive metal foil not in contact with the insulating layer is chemically polished. This is a method for manufacturing a laminate for a COF substrate in which the conductive metal foil has a thickness of 1 to 8 μm and a surface roughness Rz of 1.0 μm or less to form a conductor.
Description
本発明は、COF用途として使用するフレキシブルプリント基板用の積層体とその製造方法に関するものである。 The present invention relates to a laminate for a flexible printed circuit board used for COF applications and a method for producing the same.
テープキャリアにドライバICを実装するTAB方式(テープ・オートメイティッド・ボンディング)は、液晶表示素子(LCD)を使用するような電子産業において広く用いられている。 A TAB method (tape automated bonding) in which a driver IC is mounted on a tape carrier is widely used in the electronic industry using a liquid crystal display element (LCD).
また、近時では、より小さいスペースで、より高密度の実装を行う実装方法として、裸のICチップをフィルムキャリアテープ上に直接搭載するCOF(チップ・オン・フィルム)が開発されている。 Recently, COF (chip-on-film), in which a bare IC chip is directly mounted on a film carrier tape, has been developed as a mounting method for mounting at a higher density in a smaller space.
このCOFに用いられるフレキシブルプリント基板(FPC)は、TAB方式で用いられてきたデバイスホールを有しないため、チップ実装時の相対位置を測定する際、絶縁層を透過してドライバICチップの配線を認識する必要がある。特に、このCOFに用いられるフレキシブルプリント基板(FPC)においては、配線の狭ピッチ化が進み、微細加工が可能である必要がある。 Since the flexible printed circuit board (FPC) used in this COF does not have the device holes that have been used in the TAB method, when measuring the relative position during chip mounting, the wiring of the driver IC chip is transmitted through the insulating layer. Need to recognize. In particular, in a flexible printed circuit board (FPC) used for this COF, it is necessary that the pitch of wiring advances and fine processing is possible.
このようなCOF用のFPCに用いられる積層体としては、ポリイミドフィルムなどの絶縁フィルムにニッケルなどの密着強化層をスパッタした後、銅メッキを施した積層体がある。このような銅メッキ積層体では、ポリイミドフィルムが比較的透明であるので、IC搭載の際の位置合わせが容易ではあるが、導体と絶縁層との間の接着力が弱く、また、耐エレクトロマイグレーション性に劣るといった問題がある。 As a laminated body used for such an FPC for COF, there is a laminated body obtained by sputtering an adhesion reinforcing layer such as nickel on an insulating film such as a polyimide film and then performing copper plating. In such a copper-plated laminate, since the polyimide film is relatively transparent, the alignment during IC mounting is easy, but the adhesive force between the conductor and the insulating layer is weak, and the electromigration resistance There is a problem of inferiority.
上記のような課題を解決する積層体としては、銅箔にポリイミドフィルムを塗布法により積層したキャスティングタイプのものや、銅箔に熱可塑性樹脂や熱硬化性樹脂などを介して絶縁フィルムを熱圧着した熱圧着タイプのものなどがある。 As a laminate that solves the above-mentioned problems, a cast-type laminate in which a polyimide film is laminated on a copper foil by a coating method, or an insulating film is thermocompression bonded to the copper foil via a thermoplastic resin or a thermosetting resin. There is a thermocompression bonding type.
しかしながら、キャスティングタイプの積層体や熱圧着タイプの積層体については、導体と絶縁層との接着力の問題をある程度解消するものの、例えば銅箔をエッチングで除去した領域については、銅箔の粗度(表面粗さ)が絶縁層側に転写されてしまい、絶縁層の表面が光を乱反射して絶縁層を透過して銅パターンが認識できないといった問題がある。 However, for casting-type laminates and thermocompression-type laminates, the problem of adhesion between the conductor and the insulating layer is solved to some extent. For example, in the region where the copper foil is removed by etching, the roughness of the copper foil There is a problem that the (surface roughness) is transferred to the insulating layer side, and the surface of the insulating layer irregularly reflects light and passes through the insulating layer so that the copper pattern cannot be recognized.
そこで、特開2003−23046号公報では、導体層と絶縁層とが積層された構造を有し、この導体層の絶縁層と接する面の表面粗さが0.1〜1.8μmである積層体が開示されている。しかしながら、上記積層体は、絶縁層を透過してドライバICチップの配線を認識する問題についてはある程度解消はされるものの、例えば30μmピッチ以下を必要とするような高密度基板材料としては必ずしも満足出来るものではない。一方、特開2004-142183号公報には絶縁層と接している面の表面粗さが1.0μm以下で裏面の表面粗さが2.0μm以下である積層体が記載されている。しかしながら、絶縁層と接していない面の表面粗さが大きい場合、レジスト形成時に厚みムラが生じ、その後の配線回路のパターニング工程で回路の直線性を良好にするのが困難であった。また、導体の厚さが厚い場合にも、同様に回路の直線性の確保が難しく、特に、30μmピッチ以下の微細加工が困難であった。すなわち、絶縁層側の粗度とレジスト面側の粗度とが適切であって、微細加工の要求を満足できる積層体はなかった。
そこで、本発明では、絶縁層を透過してドライバICチップの配線を認識することが可能であると共に、導体と絶縁層との間の接着力が高く、耐エレクトロマイグレーション性に優れ、例えば30μmピッチ以下の微細加工可能な積層体とその製造方法を提供することを目的とする。 Therefore, in the present invention, it is possible to recognize the wiring of the driver IC chip through the insulating layer, and the adhesive strength between the conductor and the insulating layer is high, and the electromigration resistance is excellent, for example, a pitch of 30 μm. An object of the present invention is to provide the following microfabricated laminate and a method for producing the same.
上記問題点を解決するために、本発明者等が鋭意検討した結果、積層体を形成する導体を所定の厚みにすると共に、この導体の絶縁層と直接接している面の表面粗さRzを1.0μm以下にし、かつ、絶縁層と接していない面の表面粗さRzを1.0μm以下にすることによって、上記課題を解決し得ることを見出し、本発明を完成した。なお、表面粗さRzは「10点平均粗さ」を表し、JIS B 0601に準じて測定される。 In order to solve the above problems, the present inventors have intensively studied. As a result, the conductor forming the laminated body has a predetermined thickness, and the surface roughness Rz of the surface in direct contact with the insulating layer of the conductor is set. The inventors have found that the above problem can be solved by setting the surface roughness Rz of the surface not in contact with the insulating layer to 1.0 μm or less and 1.0 μm or less, thereby completing the present invention. The surface roughness Rz represents “10-point average roughness” and is measured according to JIS B 0601.
したがって、本発明は、導電性金属箔よりなる導体の一方の面に絶縁性樹脂よりなる絶縁層が形成されたCOF基板用積層体であって、導体の厚みが1〜8μmであり、導体の絶縁層と接している面の表面粗さRzが1.0μm以下であり、かつ、導体の絶縁層と接していない面の表面粗さRzが1.0μm以下である、COF基板用積層体である。
また、本発明は、導体の一方の面に絶縁性樹脂よりなる絶縁層が形成されたCOF基板用積層体の製造方法であって、少なくとも10μm以上の厚みを有し、かつ、一方の面の表面粗さRzが1.0μm以下である導電性金属箔の当該面に絶縁層を形成し、この絶縁層と接していない導電性金属箔の面を化学研摩してこの導電性金属箔の厚みを1〜8μmにすると共に、表面粗さRzを1.0μm以下にして導体を形成する、COF基板用積層体の製造方法である。Therefore, the present invention is a COF substrate laminate in which an insulating layer made of an insulating resin is formed on one surface of a conductor made of a conductive metal foil, the thickness of the conductor being 1 to 8 μm, This is a COF substrate laminate in which the surface roughness Rz of the surface in contact with the insulating layer is 1.0 μm or less and the surface roughness Rz of the surface not in contact with the insulating layer of the conductor is 1.0 μm or less.
Further, the present invention is a method for manufacturing a laminate for a COF substrate in which an insulating layer made of an insulating resin is formed on one surface of a conductor, and has a thickness of at least 10 μm or more. An insulating layer is formed on the surface of the conductive metal foil having a surface roughness Rz of 1.0 μm or less, and the surface of the conductive metal foil not in contact with the insulating layer is chemically polished to reduce the thickness of the conductive metal foil. This is a method for producing a laminated body for a COF substrate, wherein the conductor is formed with a surface roughness Rz of 1.0 μm or less while being 1-8 μm.
本発明では、絶縁層と直接接している導体の表面粗さRzを1.0μm以下とすることにより、仮に絶縁層との積層時に導体の粗度が絶縁層側に転写されても、絶縁層を透過してドライバICチップの配線を認識することが可能となる。また、絶縁層と直接接していない導体の表面粗度Rzが1.0μm以下とすることにより、高密度配線を必要とする場合において例えば30μmピッチ以下の加工が可能である。なお、絶縁層と直接接している導体の表面粗さRzは、絶縁層との密着性を確保するためRzは0.3μmが下限であり、絶縁層と直接接していない導体の表面粗度Rzは、後に積層される絶縁性保護膜との密着性を確保するためRzは0.1μmが下限である。 In the present invention, by setting the surface roughness Rz of the conductor in direct contact with the insulating layer to 1.0 μm or less, even if the roughness of the conductor is transferred to the insulating layer side during lamination with the insulating layer, the insulating layer The wiring of the driver IC chip can be recognized through the transmission. Further, by setting the surface roughness Rz of the conductor not in direct contact with the insulating layer to 1.0 μm or less, processing with a pitch of 30 μm or less is possible when high-density wiring is required. The surface roughness Rz of the conductor that is in direct contact with the insulating layer has a lower limit of 0.3 μm for ensuring the adhesion with the insulating layer, and the surface roughness Rz of the conductor that is not in direct contact with the insulating layer is The lower limit of Rz is 0.1 μm in order to ensure adhesion with an insulating protective film to be laminated later.
本発明における導電性金属箔よりなる導体については、例えば銅又は銅合金からなる銅箔のほか、金、銀等からなる金属箔を挙げることができ、好ましくは銅箔であるのがよい。銅箔については圧延銅箔、電解銅箔等を挙げることができるが、絶縁物である酸化物が混在するおそれを可及的に低減できる電解銅箔が更に好ましい。 Examples of the conductor made of the conductive metal foil in the present invention include a copper foil made of copper or a copper alloy, a metal foil made of gold, silver or the like, and preferably a copper foil. Examples of the copper foil include a rolled copper foil and an electrolytic copper foil, but an electrolytic copper foil that can reduce as much as possible the possibility of mixing an oxide that is an insulator is more preferable.
また、本発明においては、導体の厚みを1〜8μmとする。導体の厚みが1μmより小さいと化学研磨工程時に厚さ制御が困難であると共に信頼性を充分に得ることが出来ない。反対に8μmより大きくなると例えば30μmピッチ加工時に、導体の直線性を得る事が非常に難しくなる。 Moreover, in this invention, the thickness of a conductor shall be 1-8 micrometers. If the thickness of the conductor is smaller than 1 μm, it is difficult to control the thickness during the chemical polishing process and sufficient reliability cannot be obtained. On the other hand, if it is larger than 8 μm, it becomes very difficult to obtain the linearity of the conductor when processing a pitch of 30 μm, for example.
本発明によれば、絶縁層を透過してドライバICチップの配線を認識することが可能であり、導体と絶縁層との間の接着力が高く、耐エレクトロマイグレーション性に優れ、例えば30μmピッチ以下の微細加工が可能な積層体を得ることができる。 According to the present invention, it is possible to recognize the wiring of the driver IC chip through the insulating layer, the adhesive strength between the conductor and the insulating layer is high, the electromigration resistance is excellent, for example, 30 μm pitch or less It is possible to obtain a laminate that can be finely processed.
以下、本発明を詳細に説明する。尚、以下では電解銅箔を用いて積層体を形成する例を説明するが、本発明における積層体とこれを得るための方法については下記の内容に限定されるものではない。 Hereinafter, the present invention will be described in detail. In addition, although the example which forms a laminated body using electrolytic copper foil below is demonstrated, the laminated body in this invention and the method for obtaining this are not limited to the following content.
導電性金属箔よりなる導体として電解銅箔を用いる場合、この電解銅箔については、後に絶縁層を設ける側の面の表面粗さRzが1.0μm以下のものを使用する。これは、既に述べたように、この面に絶縁層を形成して導体を除去した際、絶縁層を透過してドライバICチップの配線の認識を可能とする為である。なお、絶縁層との密着性を確保するためにはRzは0.3μm以上であることが好ましい。また、最終的に得られる積層体における導体の厚みは1〜8μmであるが、この電解銅箔の厚みについては、後述する化学研摩を行うことから、用意する銅箔としては厚さ10μm以上、好ましくは12〜18μmの厚みのものを用いるようにするのがよい。 When an electrolytic copper foil is used as a conductor made of a conductive metal foil, the electrolytic copper foil having a surface roughness Rz of 1.0 μm or less on the surface on which an insulating layer will be provided later is used. This is because, as described above, when an insulating layer is formed on this surface and the conductor is removed, the wiring of the driver IC chip can be recognized through the insulating layer. In order to secure adhesion with the insulating layer, Rz is preferably 0.3 μm or more. Moreover, although the thickness of the conductor in the finally obtained laminate is 1 to 8 μm, the thickness of this electrolytic copper foil is subjected to chemical polishing described later, so that the prepared copper foil has a thickness of 10 μm or more, Preferably, a material having a thickness of 12 to 18 μm is used.
積層体を形成する絶縁層については、例えば熱可塑性樹脂層を有する絶縁フィルムから形成されたものであってもよく、熱硬化性樹脂層を有する絶縁フィルムから形成されたものであってもよい。また、ポリイミド前駆体樹脂溶液が導体に塗布され、このポリイミド前駆体樹脂溶液を乾燥及び硬化させることにより形成してもよい。これらのうち、好ましくは導体にポリイミド前駆体樹脂溶液が塗布された後、乾燥及び硬化させることにより絶縁層を形成したものであるのがよい。 About the insulating layer which forms a laminated body, it may be formed, for example from the insulating film which has a thermoplastic resin layer, and may be formed from the insulating film which has a thermosetting resin layer. Alternatively, the polyimide precursor resin solution may be applied to the conductor, and the polyimide precursor resin solution may be dried and cured. Of these, the insulating layer is preferably formed by drying and curing after the polyimide precursor resin solution is applied to the conductor.
上記絶縁層について、ポリイミド前駆体樹脂溶液を塗布した後、乾燥及び硬化することにより形成する場合には、公知のジアミンと酸無水物とを溶媒の存在下で重合して製造することができる。 About the said insulating layer, when apply | coating a polyimide precursor resin solution and forming by drying and hardening, it can manufacture by polymerizing a well-known diamine and an acid anhydride in presence of a solvent.
用いられるジアミンとしては、例えば、4,4’−ジアミノジフェニルエーテル、2’−メトキシ4,4’−ジアミノベンズアニリド、1,4−ビス(4−アミノフェノキシ)ベンゼン、1,3−ビス(4−アミノフェノキシ)ベンゼン、2,2’−ビス[4−(4−アミノフェノキシ)フェニル]プロパン、2,2’−ジメチル−4,4’−ジアミノビフェニル、3,3’−ジヒドロキシ−4,4’−ジアミノビフェニル、4,4’−ジアミノベンズアニリド等が挙げられる。また、酸無水物としては、例えば、無水ピロメリット酸、3,3’,4,4’−ビフェニルテトラカルボン酸二無水物、3,3’,4,4’−ジフェニルスルフォンテトラカルボン酸二無水物、4,4’−オキシジフタル酸無水物が挙げられる。ジアミン、酸無水物はそれぞれ、その1種のみを使用してもよく2種以上を併用して使用することも出来る。 Examples of the diamine used include 4,4′-diaminodiphenyl ether, 2′-methoxy 4,4′-diaminobenzanilide, 1,4-bis (4-aminophenoxy) benzene, and 1,3-bis (4- Aminophenoxy) benzene, 2,2′-bis [4- (4-aminophenoxy) phenyl] propane, 2,2′-dimethyl-4,4′-diaminobiphenyl, 3,3′-dihydroxy-4,4 ′ -Diaminobiphenyl, 4,4'-diaminobenzanilide and the like. Examples of the acid anhydride include pyromellitic anhydride, 3,3 ′, 4,4′-biphenyltetracarboxylic dianhydride, and 3,3 ′, 4,4′-diphenylsulfonetetracarboxylic dianhydride. And 4,4′-oxydiphthalic anhydride. Each of the diamine and acid anhydride may be used alone or in combination of two or more.
溶媒については、ジメチルアセトアミド、n−メチルピロリジノン、2−ブタノン、ジグライム、キシレン等が挙げられ、1種若しくは2種以上併用して使用することもできる。 Examples of the solvent include dimethylacetamide, n-methylpyrrolidinone, 2-butanone, diglyme, xylene and the like, and they can be used alone or in combination of two or more.
上記ポリイミド前駆体樹脂溶液については、前駆体状態で導体の一方の面に直接塗布することが好ましく、重合された樹脂粘度を500cps〜35,000cpsの範囲とすることが好ましい。塗布された樹脂液については熱処理を行う必要があるが、この熱処理については例えば100℃〜150℃を2分〜4分大気中で熱処理し、その後、真空加熱で室温から340℃まで昇温させ再び室温まで戻すといった処理を9時間程度行うのがよい。このようにして形成するポリイミド樹脂からなる絶縁層は、ポリイミド樹脂層の単層のみから形成してもよく、複数層から形成してもよい。ポリイミド樹脂層を複数層から形成する場合、ポリイミド樹脂層の上に異なる構成成分からなる他のポリイミド樹脂を順次塗布して形成してもよい。ポリイミド樹脂層が3層以上からなる場合、同一の構成成分からなるポリイミド樹脂を2回以上使用してもよい。 About the said polyimide precursor resin solution, it is preferable to apply | coat directly to one side of a conductor in a precursor state, and it is preferable to make the polymerized resin viscosity into the range of 500 cps-35,000 cps. The applied resin solution needs to be heat treated. For this heat treatment, for example, heat treatment is performed at 100 ° C. to 150 ° C. in the air for 2 minutes to 4 minutes, and then the temperature is raised from room temperature to 340 ° C. by vacuum heating. The process of returning to room temperature again should be performed for about 9 hours. The insulating layer made of the polyimide resin thus formed may be formed from only a single layer of the polyimide resin layer or may be formed from a plurality of layers. When the polyimide resin layer is formed from a plurality of layers, other polyimide resins made of different components may be sequentially applied on the polyimide resin layer. When the polyimide resin layer is composed of three or more layers, a polyimide resin composed of the same component may be used twice or more.
上記で得た絶縁層と導体との積層体については、絶縁層と直接接していない導体の面を化学研摩することによって、この導体の厚みを1〜8μmにすると共に、この面の表面粗さRzを1.0μm以下にする。この銅箔の表面粗さは、化学研磨の条件によっても変化するが、本発明においては、公知の研磨温度や研磨速度などの研磨条件を調整して、所望の積層体の銅箔表面粗さを調整することができる。但し、研磨液の種類と組成は、銅箔の表面粗さとの関係で重要な因子となるため、その研磨液は、過酸化水素と硫酸を主剤として含有する過酸化水素/硫酸系が好ましい。過酸化水素/硫酸系の研磨液を使用する場合、過酸化水素の濃度については70〜85g/L、硫酸の濃度については18〜22g/Lの範囲とすることが好ましい。濃度範囲が上記範囲にないと表面粗さの精密な制御が困難となる傾向にある。また、研磨温度は、20〜50℃の任意の温度で一定に保つことがよい。 For the laminate of the insulating layer and the conductor obtained above, the surface of the conductor not directly in contact with the insulating layer is chemically polished to reduce the thickness of the conductor to 1 to 8 μm and the surface roughness of this surface. Rz is set to 1.0 μm or less. The surface roughness of the copper foil varies depending on the conditions of chemical polishing. In the present invention, the copper foil surface roughness of a desired laminate is adjusted by adjusting polishing conditions such as a known polishing temperature and polishing rate. Can be adjusted. However, since the type and composition of the polishing liquid are important factors in relation to the surface roughness of the copper foil, the polishing liquid is preferably a hydrogen peroxide / sulfuric acid system containing hydrogen peroxide and sulfuric acid as main components. When using a hydrogen peroxide / sulfuric acid based polishing liquid, the concentration of hydrogen peroxide is preferably in the range of 70 to 85 g / L, and the concentration of sulfuric acid is preferably in the range of 18 to 22 g / L. If the concentration range is not within the above range, precise control of the surface roughness tends to be difficult. The polishing temperature is preferably kept constant at an arbitrary temperature of 20 to 50 ° C.
なお、上記の説明では、電解銅箔上にポリイミド樹脂を塗布することによって絶縁層を形成したが、例えば1層以上のポリイミドフィルムを電解銅箔にラミネートして絶縁層を形成し、その後、上記で説明したような化学研磨を行うようにしてもよい。 In the above description, the insulating layer is formed by applying a polyimide resin on the electrolytic copper foil. However, for example, an insulating layer is formed by laminating one or more polyimide films on the electrolytic copper foil, and then, Chemical polishing as described in (1) may be performed.
このようにして製造した積層体は、絶縁層の片面のみに電解銅箔を有する片面銅張り積層体としてもよく、また、絶縁層の両面に電解銅箔を有する両面銅張り積層体としてもよい。両面銅張り積層体については、片面銅張り積層体を形成した後、電解銅箔を熱プレスにより圧着する方法や2枚の電解銅箔の間にポリイミドフィルムを挟み熱プレスにより圧着する方法等を挙げることができる。いずれの方法においても、圧着後には、絶縁層と直接接していない電解銅箔の面の表面粗さRzを1.0μm以下にすると共にこの電解銅箔の厚みを1〜8μmの範囲となるように化学研磨を行うようにする。なお、絶縁層と直接接していない電解銅箔の表面粗さRzは後から積層される絶縁性保護膜との密着性を確保する観点から0.1μm以上であることが望ましい。 The laminate thus produced may be a single-sided copper-clad laminate having an electrolytic copper foil only on one side of the insulating layer, or a double-sided copper-clad laminate having an electrolytic copper foil on both sides of the insulating layer. . For double-sided copper-clad laminates, after forming a single-sided copper-clad laminate, a method of crimping electrolytic copper foil by hot pressing, a method of sandwiching a polyimide film between two electrolytic copper foils and crimping by hot pressing, etc. Can be mentioned. In any method, after crimping, the surface roughness Rz of the surface of the electrolytic copper foil that is not in direct contact with the insulating layer is made 1.0 μm or less and the thickness of the electrolytic copper foil is in the range of 1 to 8 μm. Do chemical polishing. Note that the surface roughness Rz of the electrolytic copper foil that is not in direct contact with the insulating layer is desirably 0.1 μm or more from the viewpoint of ensuring adhesion with an insulating protective film to be laminated later.
以下、本発明を実施例により更に詳細に説明する。 Hereinafter, the present invention will be described in more detail with reference to examples.
積層体の作成にあたり、下記4種類の銅箔を準備した。
1)銅箔1:電解銅箔 絶縁層側Rz0.7μm、レジスト面側Rz2.0μm
三井金属鉱業(株)製NA−VLP箔 厚さ15μm
2)銅箔2:電解銅箔 絶縁層側Rz1.6μm、レジスト面側Rz1.5μm
古河サーキットフォイル(株)製F2−WS箔 厚さ12μm
3)銅箔3:電解銅箔 絶縁層側Rz2.5μm、レジスト面側Rz1.5μm
三井金属鉱業(株)製SQ−VLP箔 厚さ12μm
4)銅箔4:電解銅箔 絶縁層側Rz0.8μm、レジスト面側Rz1.0μm
日本電解(株)製USLPS箔 厚さ18μmIn creating the laminate, the following four types of copper foils were prepared.
1) Copper foil 1: Electrolytic copper foil Insulation layer side Rz0.7μm, resist side Rz2.0μm
Mitsui Metal Mining Co., Ltd. NA-VLP foil thickness 15μm
2) Copper foil 2: Electrolytic copper foil Insulation layer side Rz 1.6μm, resist surface side Rz 1.5μm
F2-WS foil manufactured by Furukawa Circuit Foil Co., Ltd., thickness 12μm
3) Copper foil 3: Electrolytic copper foil Insulation layer side Rz2.5μm, resist surface side Rz1.5μm
Mitsui Kinzoku Mining Co., Ltd. SQ-VLP foil thickness 12μm
4) Copper foil 4: Electrolytic copper foil Insulation layer side Rz0.8μm, resist surface side Rz1.0μm
US Electrolytic Co., Ltd. USLPS foil thickness 18μm
[合成例1]
熱電対及び攪拌機を備えると共に窒素導入が可能な反応容器にn-メチルピロリジノンを入れた。この反応容器を容器に入った氷水に浸けた後、反応容器に無水ピロメリット酸(PMDA)を投入し、その後、4,4’-ジアミノジフェニルエーテル、(DAPE)と2 ’-メトキシ-4,4’-ジアミノベンズアニリド(MABA)を投入した。モノマーの投入総量が15wt%で、各ジアミンのモル比率(MABA:DAPE)が60:40であり、酸無水物とジアミンのモル比が0.98:1.0となるよう投入した。その後、更に攪拌を続け、反応容器内の温度が、室温から±5℃の範囲となった時に反応容器を氷水から外した。室温のまま3時間攪拌を続け、得られたポリアミック酸の溶液粘度は15,000cpsであった。[Synthesis Example 1]
N-methylpyrrolidinone was put in a reaction vessel equipped with a thermocouple and a stirrer and capable of introducing nitrogen. After soaking the reaction vessel in ice water contained in the vessel, pyromellitic anhydride (PMDA) was added to the reaction vessel, and then 4,4'-diaminodiphenyl ether, (DAPE) and 2'-methoxy-4,4 '-Diaminobenzanilide (MABA) was charged. The total amount of monomers charged was 15 wt%, the molar ratio of each diamine (MABA: DAPE) was 60:40, and the molar ratio of acid anhydride to diamine was 0.98: 1.0. Thereafter, stirring was further continued, and the reaction vessel was removed from the ice water when the temperature in the reaction vessel was in the range of room temperature to ± 5 ° C. Stirring was continued for 3 hours at room temperature, and the solution viscosity of the resulting polyamic acid was 15,000 cps.
[合成例2]
熱電対及び攪拌機を備えると共に窒素導入が可能な反応容器にn-メチルピロリジノンを入れた。この反応容器を容器に入った氷水に浸けた後、反応容器にPMDA/3, 3’,4,4’-ビフェニルテトラカルボン酸二無水物(BTDA)を投入し、その後、4,4’-ジアミノジフェニルエーテル(DAPE)を投入した。モノマーの投入総量が15wt%で、酸無水物とジアミンのモル比が1.03:1.0となるよう投入した。その後、更に攪拌を続け、反応容器内の温度が、室温から±5℃の範囲となった時に反応容器を氷水から外した。室温のまま3時間攪拌を続け、得られたポリアミック酸の溶液粘度は3,200cpsであった。[Synthesis Example 2]
N-methylpyrrolidinone was put in a reaction vessel equipped with a thermocouple and a stirrer and capable of introducing nitrogen. After immersing this reaction vessel in ice water contained in the vessel, PMDA / 3,3 ', 4,4'-biphenyltetracarboxylic dianhydride (BTDA) was charged into the reaction vessel, and then 4,4'- Diaminodiphenyl ether (DAPE) was added. The total monomer charge was 15 wt%, and the molar ratio of acid anhydride to diamine was 1.03: 1.0. Thereafter, stirring was further continued, and the reaction vessel was removed from the ice water when the temperature in the reaction vessel was in the range of room temperature to ± 5 ° C. Stirring was continued for 3 hours at room temperature, and the solution viscosity of the resulting polyamic acid was 3,200 cps.
[合成例3]
熱電対及び攪拌機を備えると共に窒素導入が可能な反応容器にn-メチルピロリジノンを入れた。この反応容器を容器に入った氷水に浸けた後、反応容器に3,3’4,4’-ジフェニルスルフォンテトラカルボン酸二無水物(DSDA)、PMDAを投入し、その後、1,3-ビス(4-アミノフェノキシ)ベンゼン(TPE-R)を投入した。モノマーの投入総量が15wt%で、各酸無水物のモル比率(DSDA:PMDA)が90:10であり、酸無水物とジアミンのモル比が1.03:1.0となるよう投入した。その後、更に攪拌を続け、反応容器内の温度が、室温から±5℃の範囲となった時に反応容器を氷水から外した。室温のまま3時間攪拌を続け、得られたポリアミック酸の溶液粘度は3,200cpsであった。[Synthesis Example 3]
N-methylpyrrolidinone was put in a reaction vessel equipped with a thermocouple and a stirrer and capable of introducing nitrogen. After immersing this reaction vessel in ice water contained in the vessel, 3,3′4,4′-diphenylsulfonetetracarboxylic dianhydride (DSDA) and PMDA were charged into the reaction vessel, and then 1,3-bis (4-Aminophenoxy) benzene (TPE-R) was added. The total monomer charge was 15 wt%, the molar ratio of each acid anhydride (DSDA: PMDA) was 90:10, and the molar ratio of acid anhydride to diamine was 1.03: 1.0. Thereafter, stirring was further continued, and the reaction vessel was removed from the ice water when the temperature in the reaction vessel was in the range of room temperature to ± 5 ° C. Stirring was continued for 3 hours at room temperature, and the solution viscosity of the resulting polyamic acid was 3,200 cps.
上記銅箔1の絶縁層側の面に合成例1〜3のポリアミック酸溶液を順次塗布し、乾燥を繰り返し、銅箔上にポリイミド前駆体樹脂層を形成した積層体を得た。この積層体を340℃で、8時間かけて熱処理し、ポリイミド樹脂層の厚みが40μm(2μm/36μm/2μm)の片面銅箔の積層体を得た。この積層体を硫酸濃度20g/L、過酸化水素濃度80g/L、添加剤濃度3%の研磨液で化学研磨し、銅箔の厚みが8.0μmになるようにすると共に、ポリイミド樹脂層と接していない銅箔の表面粗さRzが0.8μmとなるようにして導体を形成し、導体と絶縁層とからなるCOF基板用積層体を得た。 The polyamic acid solutions of Synthesis Examples 1 to 3 were sequentially applied to the surface of the copper foil 1 on the insulating layer side, and drying was repeated to obtain a laminate in which a polyimide precursor resin layer was formed on the copper foil. This laminated body was heat-treated at 340 ° C. for 8 hours to obtain a single-sided copper foil laminated body having a polyimide resin layer thickness of 40 μm (2 μm / 36 μm / 2 μm). This laminate is chemically polished with a polishing solution having a sulfuric acid concentration of 20 g / L, a hydrogen peroxide concentration of 80 g / L, and an additive concentration of 3% so that the copper foil has a thickness of 8.0 μm and is in contact with the polyimide resin layer. A conductor was formed such that the surface roughness Rz of the copper foil not formed was 0.8 μm, and a COF substrate laminate comprising a conductor and an insulating layer was obtained.
上記で得たCOF基板用積層体に配線パターンを形成してCOFフィルムキャリアテープとした。この時、インナーリード部の回路パターンを30μmピッチで作成し、錫メッキを施した後、倍率50倍のレーザー顕微鏡にて目視で回路の直線性の確認を行いライン幅が不均一な状態が観察された場合をNGとした。その後、COFフィルムキャリアテープのインナーリード部へ金バンプを有するICを実装した。実装には、フリップチップボンダー「TFC-2100」芝浦メカトロニクス(株)製を使用し、ボンディングヘッドツール温度は100℃、ステージ温度は420℃、接合圧力は1バンプ当たりの荷重が20gfになるようにして行った。この実装の際、COFフィルムキャリアテープを通してICを画像認識してICの位置合わせに用いられるアライメントマークが認識可能であるかどうかで視認性評価を行った。実装後、HHBT試験機「ETAC HIFLEX」楠本化成(株)製にて(8 5℃、85%RT、150V、1000時間)を行い、信頼性評価を行った。結果を表1に示す。 A wiring pattern was formed on the laminate for a COF substrate obtained above to obtain a COF film carrier tape. At this time, the circuit pattern of the inner lead part was created at a pitch of 30μm, tin-plated, and then the linearity of the circuit was visually confirmed with a laser microscope with a magnification of 50 times, and the line width was observed to be uneven. NG was determined as NG. Thereafter, an IC having gold bumps was mounted on the inner lead portion of the COF film carrier tape. The flip chip bonder “TFC-2100” manufactured by Shibaura Mechatronics Co., Ltd. is used for mounting, and the bonding head tool temperature is 100 ° C, the stage temperature is 420 ° C, and the bonding pressure is 20 gf per bump. I went. At the time of this mounting, visibility was evaluated by recognizing whether or not an alignment mark used for IC alignment can be recognized by recognizing an image of the IC through a COF film carrier tape. After mounting, HHBT tester “ETAC HIFLEX” manufactured by Enomoto Kasei Co., Ltd. (85 ° C., 85% RT, 150 V, 1000 hours) was used for reliability evaluation. The results are shown in Table 1.
市販のポリイミド樹脂フィルム(東レ・デュポン(株)製、商品名:カプトン150EN)を用い、片面に合成例1のポリアミック酸溶液をロールコーターにより乾燥後の厚さで2.0μmになるように塗布して150℃で2分間乾燥させた後、もう一方の面に合成例2のポリアミック酸溶液をロールコーターにより乾燥後の厚さが2.0μmになるように塗布し、70℃で5分、110℃で5分乾燥後、140℃2分、180℃5分、265℃2分、エアーフロート方式の加熱炉にて硬化を行い、合成例1のポリアミック酸溶液を塗布した側が非熱可塑性ポリイミド樹脂層であり、合成例2のポリアミック酸溶液を塗布した側が熱可塑性ポリイミド樹脂層であるポリイミドの絶縁フィルムを得た。 Using a commercially available polyimide resin film (manufactured by Toray DuPont Co., Ltd., trade name: Kapton 150EN), apply the polyamic acid solution of Synthesis Example 1 on one side to a thickness of 2.0 μm after drying with a roll coater. After drying at 150 ° C. for 2 minutes, the polyamic acid solution of Synthesis Example 2 was applied to the other surface with a roll coater so that the thickness after drying was 2.0 μm, and at 70 ° C. for 5 minutes, 110 ° C. After drying for 5 minutes at 140 ° C. for 2 minutes, 180 ° C. for 5 minutes and 265 ° C. for 2 minutes, the side coated with the polyamic acid solution of Synthesis Example 1 is a non-thermoplastic polyimide resin layer. Thus, a polyimide insulating film having a thermoplastic polyimide resin layer on the side coated with the polyamic acid solution of Synthesis Example 2 was obtained.
次いで、上記で得られた絶縁フィルムの熱可塑性ポリイミド樹脂層側の面と上記銅箔4の絶縁層側の面とを重ね合わせ、シリコンゴムで覆われたロールラミネーターを用いて240℃、圧力1.5Mpaの条件で銅箔4と上記絶縁フィルムとを貼り合わせた。その後、バッチ式のオートクレーブにて温度340℃4時間窒素雰囲気下でアニールを行って積層体を得た。この得られた積層体を実施例1と同様にして化学研磨を行い、銅箔の厚みを8.0μmとし、絶縁フィルムと接していない銅箔の表面粗さRzを0.6μmとなるようにして導体を形成し、導体と絶縁層とからなるCOF基板用積層体を得た。このCOF基板用積層体について、実施例1と同様にして実装を行い、実装時の画像認識、インナーリードの直線性及びCOF実装後信頼性について評価した。結果を表1に示す。 Next, the surface of the insulating film obtained above on the side of the thermoplastic polyimide resin layer and the surface of the copper foil 4 on the side of the insulating layer are overlapped, and using a roll laminator covered with silicon rubber, 240 ° C., pressure 1 The copper foil 4 and the said insulating film were bonded together on condition of 0.5 Mpa. Thereafter, annealing was performed in a batch-type autoclave at a temperature of 340 ° C. for 4 hours in a nitrogen atmosphere to obtain a laminate. The obtained laminate was chemically polished in the same manner as in Example 1 so that the copper foil had a thickness of 8.0 μm and the surface roughness Rz of the copper foil not in contact with the insulating film was 0.6 μm. A laminate for a COF substrate composed of a conductor and an insulating layer was obtained. The COF substrate laminate was mounted in the same manner as in Example 1, and image recognition during mounting, linearity of the inner leads, and reliability after COF mounting were evaluated. The results are shown in Table 1.
[比較例1]
上記銅箔2を用い、実施例1と同様にして積層体を形成して化学研摩を行った。得られたCOF基板用積層体の導体の厚みは8.0μmであり、絶縁層と接している側の面の表面粗さRzが1.6μm、絶縁層と接していない側(レジスト面側)の表面粗さRzが1.2μmであった。このCOF基板用積層体について、実施例1と同様にして実装を行い、実装時の画像認識、インナーリードの直線性及びCOF実装後信頼性について評価した。結果を表1に示す。[Comparative Example 1]
Using the copper foil 2, a laminate was formed in the same manner as in Example 1, and chemical polishing was performed. The thickness of the conductor of the obtained laminate for COF substrate is 8.0 μm, the surface roughness Rz of the surface in contact with the insulating layer is 1.6 μm, the surface on the side not in contact with the insulating layer (resist surface side) The roughness Rz was 1.2 μm. This COF substrate laminate was mounted in the same manner as in Example 1, and image recognition during mounting, linearity of the inner leads, and reliability after COF mounting were evaluated. The results are shown in Table 1.
[比較例2]
上記銅箔3を用い、実施例1と同様にして積層体を形成して化学研摩を行った。得られたCOF基板用積層体の導体の厚みは8.0μmであり、絶縁層と接している側の面の表面粗さRzが2.5μm、絶縁層と接していない側(レジスト面側)の表面粗さRzが0.9μmであった。このCOF基板用積層体について、実施例1と同様にして実装を行い、実装時の画像認識、インナーリードの直線性及びCOF実装後信頼性について評価した。結果を表1に示す。[Comparative Example 2]
Using the copper foil 3, a laminate was formed in the same manner as in Example 1, and chemical polishing was performed. The thickness of the conductor of the obtained laminate for COF substrate is 8.0 μm, the surface roughness Rz of the surface in contact with the insulating layer is 2.5 μm, and the surface not in contact with the insulating layer (resist surface side) The roughness Rz was 0.9 μm. This COF substrate laminate was mounted in the same manner as in Example 1, and image recognition during mounting, linearity of the inner leads, and reliability after COF mounting were evaluated. The results are shown in Table 1.
[比較例3]
銅箔4を用い、実施例1と同様にして積層体を形成した。この積層体については化学研磨を行わなかった。得られたCOF基板用積層体の導体の厚みは18μmであり、絶縁層と接している側の面の表面粗さRzが0.8μm、絶縁層と接していない側(レジスト面側)の表面粗さRzが1.0μmであった。このCOF基板用積層体について、実施例1と同様にして実装を行い、実装時の画像認識、インナーリードの直線性及びCOF実装後信頼性について評価した。結果を表1に示す。[Comparative Example 3]
A laminated body was formed using the copper foil 4 in the same manner as in Example 1. This laminated body was not subjected to chemical polishing. The thickness of the conductor of the obtained laminate for COF substrate is 18 μm, the surface roughness Rz on the surface in contact with the insulating layer is 0.8 μm, and the surface roughness on the side not in contact with the insulating layer (resist surface side) The thickness Rz was 1.0 μm. The COF substrate laminate was mounted in the same manner as in Example 1, and image recognition during mounting, linearity of the inner leads, and reliability after COF mounting were evaluated. The results are shown in Table 1.
[比較例4]
銅箔1を用いて、化学研摩を行う手前まで実施例1と同様にして積層体を作成した。次いで、この積層体を硫酸濃度80g/L、過酸化水素濃度20g/L、添加剤濃度3%の研磨液を用いて化学研磨を行い、銅箔の厚みが8.0μmになるようにすると共に、ポリイミド樹脂層と接していない銅箔の表面粗さRzが1.6μmとなるようにして導体を形成し、導体と絶縁層とからなるCOF基板用積層体を得た。このCOF基板用積層体について、実施例1と同様にして実装を行い、実装時の画像認識、インナーリードの直線性及びCOF実装後信頼性について評価した。結果を表1に示す。[Comparative Example 4]
Using the copper foil 1, a laminate was prepared in the same manner as in Example 1 until just before chemical polishing. Next, this laminate is subjected to chemical polishing using a polishing liquid having a sulfuric acid concentration of 80 g / L, a hydrogen peroxide concentration of 20 g / L, and an additive concentration of 3% so that the thickness of the copper foil becomes 8.0 μm, A conductor was formed so that the surface roughness Rz of the copper foil not in contact with the polyimide resin layer was 1.6 μm, and a COF substrate laminate comprising a conductor and an insulating layer was obtained. This COF substrate laminate was mounted in the same manner as in Example 1, and image recognition during mounting, linearity of the inner leads, and reliability after COF mounting were evaluated. The results are shown in Table 1.
Claims (6)
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JP4828439B2 (en) * | 2007-01-15 | 2011-11-30 | 新日鐵化学株式会社 | Method for producing flexible laminate |
US8238114B2 (en) | 2007-09-20 | 2012-08-07 | Ibiden Co., Ltd. | Printed wiring board and method for manufacturing same |
JP6094044B2 (en) * | 2011-03-23 | 2017-03-15 | 大日本印刷株式会社 | Heat dissipation board and element using the same |
CN103442511A (en) * | 2013-08-20 | 2013-12-11 | 珠海亚泰电子科技有限公司 | High frequency substrate |
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WO2003096776A1 (en) * | 2002-05-13 | 2003-11-20 | Mitsui Mining & Smelting Co.,Ltd. | Flexible printed wiring board for chip-on-film |
JP2004119961A (en) * | 2002-09-02 | 2004-04-15 | Furukawa Techno Research Kk | Copper foil for chip-on film, plasma display panel, and high-frequency printed wiring board |
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TW200404484A (en) * | 2002-09-02 | 2004-03-16 | Furukawa Circuit Foil | Copper foil for soft circuit board package module, for plasma display, or for radio-frequency printed circuit board |
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JP2004119961A (en) * | 2002-09-02 | 2004-04-15 | Furukawa Techno Research Kk | Copper foil for chip-on film, plasma display panel, and high-frequency printed wiring board |
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