JP5275533B2 - Metal foil laminate and prepreg - Google Patents
Metal foil laminate and prepreg Download PDFInfo
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- JP5275533B2 JP5275533B2 JP2000390802A JP2000390802A JP5275533B2 JP 5275533 B2 JP5275533 B2 JP 5275533B2 JP 2000390802 A JP2000390802 A JP 2000390802A JP 2000390802 A JP2000390802 A JP 2000390802A JP 5275533 B2 JP5275533 B2 JP 5275533B2
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- metal foil
- clad laminate
- glass cloth
- prepreg
- resin composition
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- 229910052751 metal Inorganic materials 0.000 title claims description 65
- 239000002184 metal Substances 0.000 title claims description 65
- 239000011888 foil Substances 0.000 title claims description 30
- 239000011521 glass Substances 0.000 claims description 46
- 239000004744 fabric Substances 0.000 claims description 44
- 239000011342 resin composition Substances 0.000 claims description 27
- 229920001187 thermosetting polymer Polymers 0.000 claims description 26
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 12
- 238000010438 heat treatment Methods 0.000 claims description 12
- 239000011889 copper foil Substances 0.000 claims description 10
- 238000010030 laminating Methods 0.000 claims description 9
- 238000003825 pressing Methods 0.000 claims description 8
- 238000001035 drying Methods 0.000 claims description 7
- 239000003822 epoxy resin Substances 0.000 description 23
- 229920000647 polyepoxide Polymers 0.000 description 23
- 238000004519 manufacturing process Methods 0.000 description 11
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- 239000000758 substrate Substances 0.000 description 8
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- 238000000034 method Methods 0.000 description 6
- 239000004020 conductor Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 4
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 4
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 4
- 238000005530 etching Methods 0.000 description 4
- 238000000465 moulding Methods 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- -1 Ketone compounds Chemical class 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 229930003836 cresol Natural products 0.000 description 2
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 2
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- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- VEORPZCZECFIRK-UHFFFAOYSA-N 3,3',5,5'-tetrabromobisphenol A Chemical compound C=1C(Br)=C(O)C(Br)=CC=1C(C)(C)C1=CC(Br)=C(O)C(Br)=C1 VEORPZCZECFIRK-UHFFFAOYSA-N 0.000 description 1
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical compound C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 1
- ULKLGIFJWFIQFF-UHFFFAOYSA-N 5K8XI641G3 Chemical compound CCC1=NC=C(C)N1 ULKLGIFJWFIQFF-UHFFFAOYSA-N 0.000 description 1
- 239000004953 Aliphatic polyamide Substances 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- 239000004285 Potassium sulphite Substances 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229920003231 aliphatic polyamide Polymers 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 150000001896 cresols Chemical class 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- ZZTCPWRAHWXWCH-UHFFFAOYSA-N diphenylmethanediamine Chemical compound C=1C=CC=CC=1C(N)(N)C1=CC=CC=C1 ZZTCPWRAHWXWCH-UHFFFAOYSA-N 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 230000002140 halogenating effect Effects 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 239000009719 polyimide resin Substances 0.000 description 1
- 229920001955 polyphenylene ether Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000007788 roughening Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
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- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
Landscapes
- Reinforced Plastic Materials (AREA)
- Laminated Bodies (AREA)
- Woven Fabrics (AREA)
Description
本発明は、金属箔張り積層板及びプリプレグに関する。 The present invention relates to a metal foil-clad laminate and a prepreg.
従来プリント配線板の製造に用いられる多層板の製造法の一例を以下に示す。例えば、ガラスクロス等の基材にエポキシ樹脂組成物等の熱硬化性樹脂組成物を含浸した後、加熱乾燥して半硬化させることによってプリプレグを作製し、このプリプレグを所要枚数重ねるとともに、銅箔等の金属箔をその片側又は両側に配して積層し、加熱加圧して成形を行うことによって金属箔張り積層板を作製する。そしてその金属箔張り積層板の表面の金属箔をエッチングして表面に導体回路及びプリント配線板を製造するとき用いるガイドマークを形成した内層用基板を作製した後、必要に応じて粗面化処理を行い、次いでその導体回路等を形成した内層用基板に、上記と同様にして作製したプリプレグをその片側又は両側に所要枚数重ねるとともに、必要に応じて金属箔をその片側又は両側に配して積層し、加熱加圧して成形することによって製造を行っている。 An example of the manufacturing method of the multilayer board conventionally used for manufacture of a printed wiring board is shown below. For example, after impregnating a base material such as a glass cloth with a thermosetting resin composition such as an epoxy resin composition, a prepreg is prepared by heating and drying and semi-curing, and a required number of prepregs are stacked and a copper foil A metal foil-clad laminate is prepared by arranging and laminating a metal foil such as one side or both sides of the metal foil, and heating and pressurizing. And after etching the metal foil on the surface of the metal foil-clad laminate to produce a guide mark used on the surface for producing a conductor circuit and a printed wiring board, an inner layer substrate is produced, and then a roughening treatment is performed as necessary. Then, on the inner layer substrate on which the conductor circuit and the like are formed, the required number of prepregs produced in the same manner as described above are stacked on one side or both sides, and a metal foil is disposed on one side or both sides as necessary. Manufacture is performed by laminating and molding by heating and pressing.
また、この多層板を用いてプリント配線板を製造する方法としては、内層用基板に形成したガイドマークを用い、このガイド穴を基準にドリルマシン及びレーザーマシンにて多層板に穴あけをした後、このドリルマシン及びレーザーマシンであけられた穴の壁面にスルホールメッキを施すと共に、外層の金属箔にエッチングを施して外層の導体回路を形成する方法により製造されている。 Moreover, as a method of manufacturing a printed wiring board using this multilayer board, after using the guide mark formed on the substrate for the inner layer, after drilling the multilayer board with a drill machine and a laser machine based on this guide hole, It is manufactured by a method in which through hole plating is performed on the wall surface of a hole drilled by the drill machine and the laser machine, and an outer layer metal foil is etched to form an outer layer conductor circuit.
これらの金属箔張り積層板やプリプレグの作製に用いられるガラスクロスは、平織りで織られたクロスを用いることが一般的であり、その平織りの縦糸と横糸は、同じ種類の単糸を用いて製造されている。 The glass cloth used to make these metal foil-clad laminates and prepregs is generally a cloth woven in a plain weave, and the warp and weft of the plain weave are manufactured using the same type of single yarn. Has been.
近年の電子機器の高密度化等に伴い、軽薄短小な多層プリント配線板が要求されている。そのために、パッケージの分野などでは高密度実装のために、これまで使用されてきた、TSOPやQFPに変わってBGA、CSP、Flip Chip等の形態の多層板が数多く製造されている。 With the recent increase in the density of electronic devices, there is a demand for light and thin multilayer printed wiring boards. Therefore, in the field of packages and the like, many multilayer boards in the form of BGA, CSP, Flip Chip, etc. have been manufactured in place of TSOP and QFP which have been used so far for high-density mounting.
しかし、これまでガラスクロスを用いた金属箔張り積層板やプリプレグを使用し、導体回路を形成した内層用基板とプリプレグにより、得られた多層板は実装時の加熱工程中に、多層板のそり・ねじれが大きく、その影響で実装部品の接続不良による歩留の低下、接続信頼性、電気的信頼性に問題があった。そのため、ガラスクロスを用いた金属箔張り積層板やプリプレグを使用した際に、そり・ねじれ特性に優れた多層板が得られる金属箔張り積層板やプリプレグが求められている。 However, so far, the multilayer board obtained by using a metal foil-clad laminate or prepreg using glass cloth, and the inner layer substrate and prepreg on which the conductor circuit is formed, is warped during the heating process during mounting.・ The twist was large, and this had problems in terms of yield reduction, connection reliability, and electrical reliability due to poor connection of mounted components. Therefore, when using a metal foil-clad laminate or prepreg using glass cloth, there is a need for a metal foil-clad laminate or prepreg that can provide a multilayer board with excellent warpage and twist characteristics.
本発明は、上記問題点を改善するために成されたもので、その目的とするところは、縦方向と横方向の糸の織本数を限定したガラスクロスおよび高伸び金属箔を用いた金属箔張り積層板やプリプレグを使用し、そり・ねじれ特性に優れた多層板を作製するために有用な、金属箔張り積層板およびプリプレグを提供することにある。 The present invention was made in order to improve the above problems, and the object of the present invention is to provide a metal foil using a glass cloth and a highly stretched metal foil in which the number of woven yarns in the longitudinal and transverse directions is limited. An object of the present invention is to provide a metal foil-clad laminate and a prepreg, which are useful for producing a multilayer plate excellent in warping and twisting characteristics using a stretched laminate or a prepreg.
前記課題を解決するために検討を重ねた結果、金属箔張積層板及びプリプレグの作製に用いるガラスクロスの織本数及び金属箔の伸び率が、そり・ねじれが発生する原因であることを見い出した。そして、そり・ねじれ特性に優れた多層板が得られるガラスクロスのの織本数、金属箔の伸び率の好ましい範囲を見い出し課題を解決した。 As a result of repeated studies to solve the above problems, it has been found that the number of glass cloth weaves used in the production of metal foil-clad laminates and prepregs and the elongation of the metal foil are the cause of warping and twisting. . Further, the present inventors have found a preferable range of the number of woven glass cloths and the elongation of the metal foil that can provide a multilayer board excellent in warping and twisting properties, and solved the problem.
本発明は以下(1)〜(8)に記載のものに関する。
(1) ガラスクロスに熱硬化性樹脂組成物を含浸・乾燥した後、金属箔と積層し、次いで加熱加圧して作製する金属箔張り積層板において、使用されるガラスクロスが厚み20〜200μmの平織りのガラスクロスであり、25mmあたりの縦糸の織本数と25mmあたりの横糸の織本数の和が120本以上で、該織本数の差が2本以下のガラスクロスであることを特徴とする金属箔張り積層板。
(2) 金属箔張り積層板の縦方向と横方向の熱膨張係数の差が、1ppm/℃以下であることを特徴とする(1)記載の金属箔張り積層板。
(3) 金属箔張り積層板の縦方向と横方向の弾性率の差が2GPa以下であることを特徴とする(1)又は(2)記載の金属箔張り積層板。
(4) 金属箔張り積層板及び外層に用いる金属箔の高温時の伸び率が4%〜20%であることを特徴とする(1)〜(3)のいずれかに記載の金属箔張り積層板。
(5) 金属箔が銅箔であることを特徴とする(1)〜(4)のいずれかに記載の金属箔張り積層板。
(6) ガラスクロスに熱硬化性樹脂組成物を含浸・乾燥して作製するプリプレグにおいて、使用されるガラスクロスが厚み20〜200μmの平織りのガラスクロスであり、25mmあたりの縦糸の織本数と25mmあたりの横糸の織本数の和が120本以上で、該織本数の差が2本以下のガラスクロスであることを特徴とするプリプレグ。
(7) プリプレグの縦方向と横方向の熱膨張係数の差が、1ppm/℃以下であることを特徴とする(6)記載のプリプレグ。
(8) プリプレグの縦方向と横方向の弾性率の差が2GPa以下であることを特徴とする(6)又は(7)記載のプリプレグ。The present invention relates to the following (1) to (8).
(1) In a metal foil-clad laminate produced by impregnating and drying a glass cloth with a thermosetting resin composition and then laminating with a metal foil and then heating and pressing, the glass cloth used has a thickness of 20 to 200 μm. A metal cloth characterized in that it is a glass cloth of plain weave, the sum of the number of warp yarns per 25 mm and the number of weft yarns per 25 mm is 120 or more, and the difference in the number of weaves is 2 or less Foil-clad laminate.
(2) The metal foil-clad laminate according to (1), wherein the difference between the coefficient of thermal expansion between the metal foil-clad laminate and the longitudinal direction is 1 ppm / ° C. or less.
(3) The metal foil-clad laminate according to (1) or (2), wherein the difference in elastic modulus between the longitudinal direction and the lateral direction of the metal foil-clad laminate is 2 GPa or less.
(4) The metal foil-clad laminate according to any one of (1) to (3), wherein the metal foil used for the metal foil-clad laminate and the outer layer has a high-temperature elongation rate of 4% to 20%. Board.
(5) The metal foil-clad laminate according to any one of (1) to (4), wherein the metal foil is a copper foil.
(6) In a prepreg produced by impregnating and drying a glass cloth with a thermosetting resin composition, the glass cloth used is a plain weave glass cloth having a thickness of 20 to 200 μm, and the number of warp yarns per 25 mm and 25 mm A prepreg characterized by being a glass cloth in which the sum of the number of woven yarns per round is 120 or more and the difference in the number of woven yarns is 2 or less.
(7) The prepreg according to (6), wherein the difference in thermal expansion coefficient between the longitudinal direction and the lateral direction of the prepreg is 1 ppm / ° C. or less.
(8) The prepreg according to (6) or (7), wherein the difference in elastic modulus between the longitudinal direction and the transverse direction of the prepreg is 2 GPa or less.
本発明に係る金属箔張り積層板は、平織りのガラスクロスに熱硬化性樹脂組成物を含浸・乾燥した後、金属箔と積層し、次いで加熱加圧して得られる。また、本発明に係るプリプレグは、平織りのガラスクロスに熱硬化性樹脂組成物を含浸・乾燥して得られる。 The metal foil-clad laminate according to the present invention is obtained by impregnating and drying a thermosetting resin composition on a plain weave glass cloth, laminating it with a metal foil, and then heating and pressing. The prepreg according to the present invention is obtained by impregnating and drying a thermosetting resin composition into a plain weave glass cloth.
ガラスクロスの縦方向と横方向の糸密度の比を特定の範囲とすることにより、縦方向と横方向の弾性率、熱膨張係数の差を少なくすることができる。金属箔張り積層板及びプリプレグの作製に用いるガラスクロスの織本数においては、25mmあたりの縦糸の織本数と25mmあたりの横糸の織本数の和が120本以上であり、該織本数の差が2本以下であることが必要である。該織本数の和が120本未満の場合、目曲がりなどによって歪みが発生しやすく、そりが大きくなりやすい。また、該織本数の差が2本を越える場合、異方性により、そり・ねじれが発生しやすくなる。 By setting the ratio of the yarn density in the machine direction and the machine direction of the glass cloth within a specific range, the difference in the elastic modulus and thermal expansion coefficient between the machine direction and the machine direction can be reduced. In the number of woven glass cloths used for producing the metal foil-clad laminate and prepreg, the sum of the number of warp yarns per 25 mm and the number of weft yarns per 25 mm is 120 or more, and the difference in the number of weaves is 2 It must be less than this. When the sum of the number of the weaves is less than 120, distortion is likely to occur due to bends or the like, and warpage tends to increase. Further, when the difference in the number of weaves exceeds two, warping and twisting are likely to occur due to anisotropy.
また、高伸びの金属箔を使用することで加熱成形時に発生する成形歪みを小さくすることができる。その結果、実装時の加熱工程中などで発生するそり・ねじれは小さくなり、特性向上すると考えられる。金属箔張り積層板の作製に用いる金属箔は高温時の伸びが(180℃時)4〜20%であることが好ましい。例えば銅箔の場合、4%以下の場合は効果が成形ひずみの低減効果が小さくなる。また、高温時の伸びが20%を越える銅箔は量産化されておらず、実用的でない。 In addition, by using a highly stretched metal foil, it is possible to reduce molding distortion that occurs during heat forming. As a result, warpage and torsion that occur during the heating process at the time of mounting are reduced, and it is considered that the characteristics are improved. The metal foil used for the production of the metal foil-clad laminate preferably has an elongation at high temperature (at 180 ° C.) of 4 to 20%. For example, in the case of copper foil, if it is 4% or less, the effect is less effective in reducing the molding strain. Also, copper foils with elongation at high temperatures exceeding 20% have not been mass-produced and are not practical.
本発明に用いるガラスクロスは、厚み20〜200μmのガラスクロスに限定される。ガラスクロスの厚みが20μm未満の場合はガラスクロスの製造に使用する単糸が細くなって、ガラスクロスの製造が困難となる。厚みが200μmを越えるガラスクロスを用いた場合、プリプレグや銅箔張り積層板が厚くなりすぎ、基板の重量などが不必要に大きくなる。 The glass cloth used in the present invention is limited to a glass cloth having a thickness of 20 to 200 μm. When the thickness of the glass cloth is less than 20 μm, the single yarn used for the production of the glass cloth becomes thin, and the production of the glass cloth becomes difficult. When a glass cloth having a thickness exceeding 200 μm is used, the prepreg or the copper foil-clad laminate becomes too thick, and the weight of the substrate becomes unnecessarily large.
また、本発明に用いるガラスクロスは、ガラスクロスの縦糸と横糸が共にJIS規格R3413に規定される単糸であることが好ましい。この単糸を用いて厚み20〜200μmの平織りのガラスクロスを製造すると、ガラスクロスに含浸する熱硬化性樹脂組成物の比率を、成形するのに適度な範囲に製造することができ好ましい。 Moreover, it is preferable that the glass cloth used for this invention is a single yarn by which both the warp and the weft of glass cloth are prescribed | regulated to JIS specification R3413. It is preferable to produce a plain weave glass cloth having a thickness of 20 to 200 μm using this single yarn because the ratio of the thermosetting resin composition impregnated into the glass cloth can be produced in an appropriate range for molding.
本発明に用いられる熱硬化性樹脂組成物としては、金属箔張り積層板の製造に用いる熱硬化性樹脂組成物及びプリプレグの製造に用いる熱硬化性樹脂組成物共に、エポキシ樹脂系、フェノール樹脂系、ポリイミド樹脂系、不飽和ポリエステル樹脂系、ポリフェニレンエーテル樹脂系等の単独、変性物、混合物のように、一般に積層板の作成に利用可能な熱硬化性樹脂全般を用いることができる。なお、金属箔張り積層板の製造に用いる熱硬化性樹脂組成物及びプリプレグの製造に用いる熱硬化性樹脂組成物は、同じものでもよく、異なる樹脂組成物でもよい。 As the thermosetting resin composition used in the present invention, both the thermosetting resin composition used for the production of the metal foil-clad laminate and the thermosetting resin composition used for the production of the prepreg are epoxy resin type, phenol resin type. Generally, thermosetting resins that can be generally used for the production of laminates can be used, such as polyimide resins, unsaturated polyester resins, polyphenylene ether resins, and the like alone, modified products, and mixtures. The thermosetting resin composition used for producing the metal foil-clad laminate and the thermosetting resin composition used for producing the prepreg may be the same or different resin compositions.
この熱硬化性樹脂組成物中には、熱硬化性樹脂を必須として含有し、必要に応じてその熱硬化性樹脂の硬化剤、硬化促進剤、無機充填材及び溶剤等を含有することができる。なおエポキシ樹脂等のように自己硬化性の低い熱硬化性樹脂は、その樹脂を硬化するための硬化剤等も含有することが必要である。 The thermosetting resin composition contains a thermosetting resin as an essential component, and can contain a curing agent, a curing accelerator, an inorganic filler, a solvent, and the like of the thermosetting resin as necessary. . Note that a thermosetting resin with low self-curing property such as an epoxy resin needs to contain a curing agent for curing the resin.
なお、熱硬化性樹脂組成物が、エポキシ樹脂系の場合、電気特性及び接着性のバランスが良好であり、好ましい。エポキシ樹脂系の樹脂組成物に含有するエポキシ樹脂としては、例えばビスフェノールA型エポキシ樹脂、ビスフェノールF型エポキシ樹脂、ビスフェノールS型エポキシ樹脂、フェノールノボラック型エポキシ樹脂、ビスフェノールAノボラック型エポキシ樹脂、ビスフェノールFノボラック型エポキシ樹脂、クレゾールノボラック型エポキシ樹脂、ジアミノジフェニルメタン型エポキシ樹脂、及びこれらのエポキシ樹脂構造体中の水素原子の一部をハロゲン化することにより難燃化したエポキシ樹脂等が挙げられる。また、このエポキシ樹脂系の樹脂組成物に含有する硬化剤としては、例えばジシアンジアミド、脂肪族ポリアミド等のアミド系硬化剤や、アンモニア、トリエチルアミン、ジエチルアミン等のアミン系硬化剤や、フェノールノボラック樹脂、クレゾールノボラック樹脂、p−キシレン−ノボラック樹脂等のフェノール系硬化剤や、酸無水物類等が挙げられる。 In addition, when a thermosetting resin composition is an epoxy resin type | system | group, the balance of an electrical property and adhesiveness is favorable, and it is preferable. Examples of the epoxy resin contained in the epoxy resin-based resin composition include bisphenol A type epoxy resin, bisphenol F type epoxy resin, bisphenol S type epoxy resin, phenol novolac type epoxy resin, bisphenol A novolac type epoxy resin, and bisphenol F novolak. Type epoxy resin, cresol novolac type epoxy resin, diaminodiphenylmethane type epoxy resin, and epoxy resin made flame retardant by halogenating a part of hydrogen atoms in these epoxy resin structures. Examples of the curing agent contained in the epoxy resin-based resin composition include amide-based curing agents such as dicyandiamide and aliphatic polyamide, amine-based curing agents such as ammonia, triethylamine, and diethylamine, phenol novolac resins, and cresols. Examples thereof include phenolic curing agents such as novolak resin and p-xylene-novolak resin, and acid anhydrides.
上記熱硬化性樹脂組成物に含有することができる無機充填材としては、シリカ、炭酸カルシウム、水酸化アルミニウム、タルク等の無機質粉末充填材や、ガラス繊維、パルプ繊維、合成繊維、セラミック繊維等の繊維質充填材が挙げられ、また、上記熱硬化性樹脂組成物に含有することができる溶剤としてはN,N−ジメチルホルムアミド等のアミド類、エチレングリコールモノメチルエーテル等のエーテル化合物、アセトン、メチルエチルケトン等のケトン化合物、メタノール、エタノール等のアルコール化合物、ベンゼン、トルエン等の芳香族炭化水素化合物等が挙げられる。 Examples of inorganic fillers that can be contained in the thermosetting resin composition include inorganic powder fillers such as silica, calcium carbonate, aluminum hydroxide, and talc, and glass fibers, pulp fibers, synthetic fibers, ceramic fibers, and the like. Examples of the solvent that can be contained in the thermosetting resin composition include amides such as N, N-dimethylformamide, ether compounds such as ethylene glycol monomethyl ether, acetone, methyl ethyl ketone, and the like. Ketone compounds, alcohol compounds such as methanol and ethanol, and aromatic hydrocarbon compounds such as benzene and toluene.
この熱硬化性樹脂組成物をガラスクロスに含浸する方法としては特に限定するものではなく、一般の方法が適用可能である。なお、熱硬化性樹脂組成物をガラスクロスに含浸した後、必要に応じて加熱乾燥していてもよい。 A method for impregnating the glass cloth with the thermosetting resin composition is not particularly limited, and a general method is applicable. In addition, after impregnating the thermosetting resin composition in the glass cloth, you may heat-dry as needed.
本発明に用いられる金属箔としては銅、アルミニウム、真鍮、ニッケル等の単独、合金、複合の金属箔を用いることができ、金属箔の代わりに金属箔が積層成形された片面金属箔張り積層板、両面金属箔張り積層板を用いることもできる。なお、この金属箔は、金属箔張り積層板の作製のみに用いることに限定するものではなく、内層用基板とプリプレグとを積層したその積層物の片側又は両側に積層して用いてもよい。金属箔の厚みとしては、特に制限はされないが、金属箔張り積層板の作製に用いる場合は0.009〜0.070mmが、内層用基板とプリプレグとを積層したその積層物の片側又は両側に積層する場合は0.009〜0.035mmが一般的であり、本発明においてもこれらに従った金属箔を使用することが好ましい。 The metal foil used in the present invention can be a single, alloy, or composite metal foil of copper, aluminum, brass, nickel, etc., and a single-sided metal foil-clad laminate in which a metal foil is laminated and formed instead of the metal foil A double-sided metal foil-clad laminate can also be used. In addition, this metal foil is not limited to use only for preparation of a metal foil-clad laminate, and may be used by being laminated on one side or both sides of the laminate obtained by laminating an inner layer substrate and a prepreg. Although it does not restrict | limit especially as thickness of metal foil, When using for preparation of a metal foil tension laminated board, 0.009-0.070mm is the one side or both sides of the laminated body which laminated | stacked the board | substrate for inner layers, and the prepreg. When laminating, 0.009 to 0.035 mm is common, and it is preferable to use a metal foil according to these also in the present invention.
金属箔張り積層板を製造するときの加熱加圧する条件、及び内層用基板とプリプレグとを積層した後の加熱加圧する条件としては、熱硬化性樹脂組成物が硬化する条件で適宜調整して加熱加圧すればよいが、加圧の圧力が高いと導体回路の寸法収縮のばらつきが大きくなる場合があるため、成形性を満足する範囲内で、できるだけ低圧で加圧することが好ましい。なお、加熱加圧を300Torr以下の減圧雰囲気下で行うと、成形性が良好となり、好ましい。 Conditions for heating and pressing when producing a metal foil-clad laminate and conditions for heating and pressing after laminating the substrate for the inner layer and the prepreg are appropriately adjusted and heated under conditions for curing the thermosetting resin composition. Although pressurization may be performed, if the pressurization pressure is high, the dimensional shrinkage variation of the conductor circuit may increase. Therefore, it is preferable to pressurize as low pressure as possible within a range satisfying the moldability. Note that it is preferable to perform heating and pressing in a reduced-pressure atmosphere of 300 Torr or less because moldability is improved.
金属箔張り積層板表面に回路形成する際に金属箔をエッチングする方法としては、特に限定するものではなく、金属箔及びそのエッチングに用いるエッチングレジストに合わせて、一般に用いられている方法を適用することができ、回路形成することによってプリント配線板とすることができる。こうして得られたプリント配線板は、さらに絶縁フィルムや本発明によるプリプレグを積層し、その外層にさらに回路形成するなど、一般に知られている方法で多層化して多層配線板とすることもできる。 The method for etching the metal foil when forming a circuit on the surface of the metal foil-clad laminate is not particularly limited, and a generally used method is applied according to the metal foil and the etching resist used for the etching. It is possible to form a printed wiring board by forming a circuit. The printed wiring board thus obtained can be multilayered by a generally known method such as further laminating an insulating film or the prepreg according to the present invention and further forming a circuit on the outer layer thereof to form a multilayer wiring board.
(実施例1)
JIS規格R3413に規定されるE225 1/0の単糸を縦糸及び横糸に用いて、縦糸の糸密度を25mm当たり61本、横糸の糸密度を25mm当たり59本となるように織って平織りのガラスクロスを得た。なお、糸密度の比は(縦糸)/(横糸)=1.03/1である。また、このガラスクロスの厚みをJIS規格R3420に従い測定したところ95μmであり、ガラスクロスの重量をIPC規格EG−140に従い測定したところ107.9g/平方mであった。Example 1
Plain weave glass using E225 1/0 single yarn specified in JIS standard R3413 for warp and weft yarns so that the warp yarn density is 61 per 25 mm and the weft yarn density is 59 per 25 mm. Got a cross. The ratio of yarn density is (warp yarn) / (weft yarn) = 1.03 / 1. Further, the thickness of the glass cloth was measured according to JIS standard R3420 to be 95 μm, and the weight of the glass cloth was measured according to IPC standard EG-140 to be 107.9 g / square m.
熱硬化性樹脂組成物として、下記のエポキシ樹脂2種類、硬化剤、硬化促進剤及び溶剤2種類よりなるエポキシ樹脂系樹脂組成物を使用した。
・エポキシ樹脂1:テトラブロモビスフェノールA型エポキシ樹脂[東都化成株式会社製、商品名YDB−500]を固形分として87.5重量部
・エポキシ樹脂2:クレゾールノボラック型エポキシ樹脂[東都化成株式会社製、商品名YDCN−220]を固形分として12.5重量部
・硬化剤:ジシアンジアミドを2.8重量部
・硬化促進剤:2−エチル−4−メチルイミダゾールを0.18重量部
・溶剤:N,N−ジメチルホルムアミドを25重量部。
・溶剤2:メチルエチルケトンを100重量部。As the thermosetting resin composition, an epoxy resin resin composition composed of the following two epoxy resins, a curing agent, a curing accelerator, and two solvents was used.
Epoxy resin 1: Tetrabromobisphenol A type epoxy resin [manufactured by Toto Kasei Co., Ltd., trade name YDB-500] 87.5 parts by weight as a solid content Epoxy resin 2: Cresol novolac type epoxy resin [manufactured by Toto Kasei Co., Ltd. , Trade name YDCN-220] as a solid content, 12.5 parts by weight, curing agent: 2.8 parts by weight of dicyandiamide, curing accelerator: 0.18 parts by weight of 2-ethyl-4-methylimidazole, solvent: N , 25 parts by weight of N-dimethylformamide.
Solvent 2: 100 parts by weight of methyl ethyl ketone.
この樹脂組成物を、上記ガラスクロスに、乾燥後の熱硬化性樹脂組成物の量が、熱硬化性樹脂組成物及びガラスクロスの合計100重量部に対し、52重量部となるように調整して含浸した後、最高温度165℃で乾燥してプリプレグを作製した。 The resin composition was adjusted so that the amount of the thermosetting resin composition after drying was 52 parts by weight with respect to the total of 100 parts by weight of the thermosetting resin composition and the glass cloth. After impregnation, the product was dried at a maximum temperature of 165 ° C. to prepare a prepreg.
次いで得られたプリプレグを所定枚数重ね、両側に厚み12μm(180℃時伸び=2.0%)の銅箔を配して積層した後、この積層物を金属プレートで挟み、最高温度180℃、圧力3.0MPaで90分加熱加圧して成形して両面銅張り積層板を作製した。 Next, a predetermined number of the obtained prepregs were stacked, and a copper foil having a thickness of 12 μm (elongation at 180 ° C. = 2.0%) was placed on both sides and laminated. A double-sided copper-clad laminate was formed by heating and pressing at a pressure of 3.0 MPa for 90 minutes.
(実施例2)
実施例1と同様のガラスクロスを用い、両側に厚み12μm(180℃時伸び=4.0%)の銅箔を配して積層したこと以外は実施例1と同様にして両面銅張積層板を得た。(Example 2)
Double-sided copper-clad laminate in the same manner as in Example 1 except that the same glass cloth as in Example 1 was used and a copper foil having a thickness of 12 μm (elongation at 180 ° C. = 4.0%) was arranged on both sides and laminated. Got.
(実施例3)
実施例1と同様のガラスクロスを用い、両側に厚み12μm(180℃時伸び=8.0%)の銅箔を配して積層したこと以外は実施例1と同様にして両面銅張積層板を得た。(Example 3)
Double-sided copper-clad laminate as in Example 1 except that the same glass cloth as in Example 1 was used and a copper foil having a thickness of 12 μm (elongation at 180 ° C. = 8.0%) was arranged on both sides and laminated. Got.
(実施例4)
実施例1と同様のガラスクロスを用い、両側に厚み12μm(180℃時伸び=12.0%)の銅箔を配して積層したこと以外は実施例1と同様にして両面銅張積層板を得た。Example 4
Double-sided copper-clad laminate in the same manner as in Example 1 except that the same glass cloth as in Example 1 was used and a copper foil having a thickness of 12 μm (elongation at 180 ° C. = 12.0%) was disposed on both sides. Got.
(比較例1)
縦糸の糸密度を25mm当たり66本、横糸の糸密度を25mm当たり55本となるように織ってガラスクロスを得たこと以外は実施例1と同様にして両面銅張り積層板を得た。なお、糸密度の比は(縦糸)/(横糸)=1.20/1である。また、このガラスクロスを実施例1と同様にして測定したところ、厚み95μm、重量107.6g/平方mであった。(Comparative Example 1)
A double-sided copper-clad laminate was obtained in the same manner as in Example 1 except that a glass cloth was obtained by weaving so that the warp yarn density was 66 per 25 mm and the weft yarn density was 55 per 25 mm. The ratio of yarn density is (warp yarn) / (weft yarn) = 1.20 / 1. The glass cloth was measured in the same manner as in Example 1. The thickness was 95 μm and the weight was 107.6 g / square m.
実施例1〜4及び比較例1で得られた多層板について曲げ弾性率、熱膨張係数及びそり量を測定した。熱膨張係数の測定方法は、TMAを用いてJIS-C6481に準拠し測定を行った。そり量の測定は、各10枚行いその平均値をその多層板のそり量とした。また、そり量の測定方法は、得られた積層板を35×31mmに切断し、銅箔を全面エッチングした後、定盤の上に置き、接触式表面粗さ計ではね上がり量の一番大きい部分と一番小さい部分の間隔を反り量として測定した。 The multilayered boards obtained in Examples 1 to 4 and Comparative Example 1 were measured for flexural modulus, thermal expansion coefficient and warpage. The measurement method of the thermal expansion coefficient was measured based on JIS-C6481 using TMA. The amount of warpage was measured for 10 sheets each, and the average value was taken as the amount of warpage of the multilayer board. In addition, the method for measuring the amount of warpage is that the obtained laminate is cut to 35 × 31 mm, the copper foil is etched on the entire surface, then placed on a surface plate, and the largest amount of protrusion by the contact-type surface roughness meter. The distance between the portion and the smallest portion was measured as the amount of warpage.
結果は表1に示した通り、各実施例は比較例1と比べ弾性率・熱膨張係数の縦横の差が小さく、反り量が小さくなることが確認された。 As shown in Table 1, it was confirmed that each example had a smaller vertical / horizontal difference in elastic modulus and thermal expansion coefficient and a smaller amount of warpage than Comparative Example 1.
本発明のプリプレグ及び金属箔張り積層板は、ガラスクロスが厚み20μm以上であることから、機械強度を損なうこと無く、また、ガラスクロスの縦方向と横方向の25mmあたりの糸密度の差を2本以下としたガラスクロスを用いることにより、異方性が小さく、そり・ねじれが低減される。 In the prepreg and the metal foil-clad laminate of the present invention, since the glass cloth has a thickness of 20 μm or more, the difference in the yarn density per 25 mm in the vertical direction and the horizontal direction of the glass cloth is 2 without impairing the mechanical strength. By using the glass cloth below this, the anisotropy is small, and warpage and twisting are reduced.
Claims (4)
In a metal foil-clad laminate produced by impregnating and drying a glass cloth with a thermosetting resin composition, laminating with a metal foil, and then heating and pressing, the glass cloth used is a plain weave glass with a thickness of 20 to 200 μm a cross, a sum of weft woven number per weave number and 25mm warp per 25mm 120 or more, the difference in woven number is Ri glass cloth der below two, the metal foil used is , metal foil-clad laminate elongation at high temperature, characterized in 4% to 12% of the metal foil der Rukoto.
2. The metal foil-clad laminate according to claim 1, wherein the difference in thermal expansion coefficient between the metal foil-clad laminate and the longitudinal direction is 1 ppm / ° C. or less.
The metal foil-clad laminate according to claim 1 or 2, wherein the difference in elastic modulus between the longitudinal direction and the lateral direction of the metal-foil-clad laminate is 2 GPa or less.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2000390802A JP5275533B2 (en) | 2000-12-22 | 2000-12-22 | Metal foil laminate and prepreg |
Applications Claiming Priority (1)
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JP2000390802A JP5275533B2 (en) | 2000-12-22 | 2000-12-22 | Metal foil laminate and prepreg |
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JP2002194120A JP2002194120A (en) | 2002-07-10 |
JP5275533B2 true JP5275533B2 (en) | 2013-08-28 |
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JP2000390802A Expired - Lifetime JP5275533B2 (en) | 2000-12-22 | 2000-12-22 | Metal foil laminate and prepreg |
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CN103582664B (en) * | 2011-05-27 | 2016-03-23 | 三菱瓦斯化学株式会社 | Resin combination, prepreg and veneer sheet |
JP2013014744A (en) * | 2011-06-10 | 2013-01-24 | Sumitomo Bakelite Co Ltd | Glass woven fabric, transparent glass fiber composite resin sheet, display device, and solar cell |
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JP3638635B2 (en) * | 1994-07-01 | 2005-04-13 | 株式会社有沢製作所 | Printed circuit board |
JPH10272733A (en) * | 1997-03-31 | 1998-10-13 | Hitachi Chem Co Ltd | Manufacture of metal-clad laminate |
JPH11195853A (en) * | 1998-01-06 | 1999-07-21 | Asahi Schwebel Co Ltd | Printed-wiring board |
JP3023427B2 (en) * | 1998-02-27 | 2000-03-21 | 旭シュエーベル株式会社 | Glass cloth and printed wiring board |
US7049253B1 (en) * | 1999-04-05 | 2006-05-23 | Asahi-Schwebel Co., Ltd. | Glass cloth and printed wiring board |
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