JPH01294017A - Preparation of laminated sheet - Google Patents
Preparation of laminated sheetInfo
- Publication number
- JPH01294017A JPH01294017A JP12645688A JP12645688A JPH01294017A JP H01294017 A JPH01294017 A JP H01294017A JP 12645688 A JP12645688 A JP 12645688A JP 12645688 A JP12645688 A JP 12645688A JP H01294017 A JPH01294017 A JP H01294017A
- Authority
- JP
- Japan
- Prior art keywords
- molding
- temp
- laminated sheet
- highest
- resin
- 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.)
- Pending
Links
- 238000000465 moulding Methods 0.000 claims abstract description 24
- 239000000463 material Substances 0.000 claims abstract description 11
- 229910052751 metal Inorganic materials 0.000 claims abstract description 8
- 239000002184 metal Substances 0.000 claims abstract description 8
- 238000000034 method Methods 0.000 claims description 5
- 239000011888 foil Substances 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract description 7
- 229910052742 iron Inorganic materials 0.000 abstract description 3
- 239000010935 stainless steel Substances 0.000 abstract description 2
- 229910001220 stainless steel Inorganic materials 0.000 abstract description 2
- 238000000748 compression moulding Methods 0.000 abstract 1
- 230000003247 decreasing effect Effects 0.000 abstract 1
- 238000004904 shortening Methods 0.000 abstract 1
- 229920005989 resin Polymers 0.000 description 7
- 239000011347 resin Substances 0.000 description 7
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000003822 epoxy resin Substances 0.000 description 3
- 239000004744 fabric Substances 0.000 description 3
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 3
- 239000010931 gold Substances 0.000 description 3
- 229910052737 gold Inorganic materials 0.000 description 3
- 238000003475 lamination Methods 0.000 description 3
- 239000000123 paper Substances 0.000 description 3
- -1 polybutylene terephthalate Polymers 0.000 description 3
- 229920000647 polyepoxide Polymers 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 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 1
- 229920000742 Cotton Polymers 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004696 Poly ether ether ketone Substances 0.000 description 1
- 239000004962 Polyamide-imide Substances 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004734 Polyphenylene sulfide Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 238000005253 cladding Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000011889 copper foil Substances 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000013013 elastic material Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000012784 inorganic fiber Substances 0.000 description 1
- 239000002655 kraft paper Substances 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 239000011120 plywood Substances 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920002312 polyamide-imide Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920002530 polyetherether ketone Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920006380 polyphenylene oxide Polymers 0.000 description 1
- 229920000069 polyphenylene sulfide Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 238000009824 pressure lamination Methods 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- 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
- H05K3/02—Apparatus or processes for manufacturing printed circuits in which the conductive material is applied to the surface of the insulating support and is thereafter removed from such areas of the surface which are not intended for current conducting or shielding
- H05K3/022—Processes for manufacturing precursors of printed circuits, i.e. copper-clad substrates
Landscapes
- Casting Or Compression Moulding Of Plastics Or The Like (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明はvIL気機器機器算機語、過言機器等に用いら
れるWLgC用積層板積層板方法に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a method for laminating a laminate for WLgC used for VIL equipment, computer equipment, exaggeration equipment, and the like.
従来、vItgC用積層板は樹脂含浸基材、金属箔から
なる積層体を金属プレートに挾んだものを5〜20組重
ねた外側にクラン四ン材を介してキャリア板を配し熱盤
間に挾み成形最高温度で所要成形時間加熱加圧積層成形
して得られるものであるが、熱盤間に挿入する積層体の
組数を多くする程、熱盤付近の積層体と熱盤間中央付近
の積層体との伝熱量の差からくる積層板性能のバフツキ
は避けられないものであった。Conventionally, vItgC laminates have been made by stacking 5 to 20 sets of laminates consisting of a resin-impregnated base material and metal foil sandwiched between metal plates, and placing a carrier plate on the outside with cranium material interposed between the hot plates. It is obtained by heat and pressure lamination molding at the maximum temperature for the required forming time, but as the number of laminates inserted between the hot plates increases, the distance between the laminates near the hot plate and the hot platen increases. Buffiness in the performance of the laminate due to the difference in heat transfer with the laminate near the center was unavoidable.
従来の技術で述べたようにプレス熱盤間に挿入する積層
体の組数を多くする程、積層板性能のバフツキが発生す
る。この対策として樹脂含浸基材の樹脂含有量、硬化度
を検討したり、途!+温、全外圧成形を検討したが性能
バフツキをなくすることはできず、むしろ成形時間の延
長化という問題が発生した。本発明は従来の技術におけ
る上述の問題点に鑑みてなされたもので、その目的とす
るところは性能バラツキのないIfIHI板の製造方法
を提供することにある。As described in the related art section, the larger the number of laminates inserted between press hot platens, the more buffiness occurs in the performance of the laminates. As a countermeasure to this problem, we need to consider the resin content and degree of curing of the resin-impregnated base material. + temperature, full external pressure molding was considered, but it was not possible to eliminate the performance buffiness, and rather the problem of prolonging the molding time occurred. The present invention has been made in view of the above-mentioned problems in the prior art, and its purpose is to provide a method for manufacturing IfIHI boards without variations in performance.
本発明はプレス熱盤間に樹脂含浸基材、金(箔からなる
積層体多数を重ね、各積、1体の上面及び又は下面に金
属プレートを配設して積層成形するに際し、成形最高温
度での所要成形時間を3〜50%短縮し、短縮分は成形
最高温度よ910〜40°C低温に放冷後、その温度に
保持することを特徴とする積層板の製造方法のため、熱
盤間積層体全体の圧力、熱量の伝達を均一にすることが
でき、従って熱盤間で多数得られる積層板の性能バフツ
キをなくすることができたもので、以下本発明の詳細な
説明する。In the present invention, a large number of laminates made of a resin-impregnated base material and gold (foil) are stacked between press hot platens, and a metal plate is placed on the top and/or bottom of each laminate. The required molding time is reduced by 3 to 50%, and the shortened amount is reduced by 910 to 40 degrees Celsius below the maximum molding temperature. It is possible to make the pressure and heat transfer uniform throughout the inter-plate laminated body, and therefore it is possible to eliminate the performance buffiness of the laminated plates obtained in many cases between the hot plates.The present invention will be described in detail below. .
本発明に用いる樹脂含浸基材の樹脂としては、フェノ−
/L/樹脂、クレゾール樹脂、エポキシ樹脂、不飽和ポ
リエステル樹脂、メラミン樹脂、ポリイミド、ポリブタ
ジェン、ポリアミド、ポリアミドイミド、ポリスルフォ
ン、ポリフェニレンサルファイド、ポリフェニレンオキ
サイド、ポリブチレンテレフタレート、ポリエーテルエ
ーテルケトン、弗化樹脂等の単独、変性物、混合物等が
用いられ必要に応じて粘度調整に水、メチルアルコール
、アセトン、シクロヘキサノン、スチレン等の溶媒を添
加したもので、基材としては、がフス、アスベスト等の
無機繊維やポリエステル、ポリアミにポリビニルアルコ
ール、アクリル等の有機合成繊維や木綿等の天然繊維か
らなる織布、不織布、マット或は紙又はこれらの組合せ
基材等である。金11i[、!:しては銅、アルミニウ
ム、鉄、ニッケル、亜鉛等の単独、合金、複合品であシ
、必要に応じて接着面を化学処理及び又は物理処理し更
に必要に応じて接着剤層を設けたものである。金属プレ
ートとしては厚さ1〜2Mの鉄、アルミニウム、鋼、ニ
ッケル等の単独、合金、複合品であり、必要に応じて表
面に雌型層を設けることができる。成形最高温度での所
要成形時間は25−50%短縮することが必要である。As the resin for the resin-impregnated base material used in the present invention, phenol
/L/Resin, cresol resin, epoxy resin, unsaturated polyester resin, melamine resin, polyimide, polybutadiene, polyamide, polyamideimide, polysulfone, polyphenylene sulfide, polyphenylene oxide, polybutylene terephthalate, polyether ether ketone, fluorinated resin, etc. It is used alone, modified products, mixtures, etc., and if necessary, a solvent such as water, methyl alcohol, acetone, cyclohexanone, styrene, etc. is added to adjust the viscosity.As a base material, inorganic fibers such as sulfur, asbestos, etc. The base materials include woven fabrics, nonwoven fabrics, mats, paper, or combinations thereof made of organic synthetic fibers such as polyester, polyamide, polyvinyl alcohol, acrylic, and natural fibers such as cotton. Gold 11i[,! : Single, alloy, or composite products of copper, aluminum, iron, nickel, zinc, etc. The adhesive surface is chemically and/or physically treated as necessary, and an adhesive layer is provided as necessary. It is something. The metal plate may be made of iron, aluminum, steel, nickel, etc. alone, alloy, or composite with a thickness of 1 to 2M, and a female layer may be provided on the surface if necessary. The required molding time at the maximum molding temperature needs to be reduced by 25-50%.
即ち25%未満では熱盤間の多数の積層体への圧力、熱
量を充分均一化することができず、50%をこえると積
層板の硬化が不充分になるからである。クッシ璽ン材と
してはゴム、合成m指、紙、布、板、合板、樹脂含浸紙
布のように弾性を有するものであればよく、厚みは1〜
1゜顛であることが好ましい。キャリア板については通
常のものをその41ま用いることができる。That is, if it is less than 25%, it will not be possible to sufficiently uniformize the pressure and heat applied to the large number of laminates between the hot platens, and if it exceeds 50%, the curing of the laminates will be insufficient. The material for the cushion may be any elastic material such as rubber, synthetic rubber, paper, cloth, board, plywood, or resin-impregnated paper cloth, and the thickness is 1 to 1.
Preferably, the size is 1°. As for the carrier plate, up to 41 ordinary ones can be used.
以下本発明を実施例にもとづいて説明する。The present invention will be explained below based on examples.
実施例1
厚さ0.2Hのガラス布に、エポキシ樹脂(シェル化学
株式会社・埒、品名エピコート1001 ) 100重
賦部(以下単に部と記す)、ジンアンジアミド4部、ベ
ンジルジメチルアミン0.2部、メチルオキシド−A/
100部からなるエポキシ樹脂ワニスを、乾燥後樹脂
量が(資)重量%(以下単に客と記す)になるように含
浸、乾燥して得意樹脂含浸基材7枚の上、下面に厚さ0
.035ggの銅箔を夫々配設した積り体を厚さIff
のステンレスm喪金・寓プレートに挾んだもの金lO姐
重ねた外側に厚みムブ1lrIIの厚さ10Hのクラフ
ト紙りツ!/=Iン材分介し厚さ5騙の鉄環キャリア板
を配設してから熱盤間に挾み、成形圧力40kg層、1
80”Cで70分間(々Q1成形成形部圧下のまま放冷
し10分間で170″Cに!14温させ、加圧下のまま
170°Cでり分間積、1成形して10吹の厚さ1.6
allの両面鋼張がフス′)&材エボキン樹脂端層板を
得た。Example 1 A glass cloth with a thickness of 0.2H was coated with 100 parts of an epoxy resin (Shell Chemical Co., Ltd., product name: Epicoat 1001), 4 parts of dianediamide, and 0.0 parts of benzyldimethylamine. 2 parts, methyl oxide-A/
The epoxy resin varnish consisting of 100 parts was impregnated so that the resin amount after drying was % by weight (hereinafter simply referred to as customer), and dried to coat the upper and lower surfaces of 7 resin-impregnated substrates with a thickness of 0.
.. 035gg of copper foil is arranged on each stack with a thickness of Iff.
10H thick kraft paper with a thickness of 1lrII on the outside, sandwiched between stainless steel mourning metal plates and overlaid gold 1O2! / = Insert an iron ring carrier plate with a thickness of 5 mm, sandwich it between hot plates, and apply a molding pressure of 40 kg to 1 layer.
80"C for 70 minutes (Q1 molding part left to cool under pressure and reached 170"C in 10 minutes! 14 Warm it to 170"C while under pressure. Volume for 1 minute, 1 mold and 10 blows. Sa1.6
All double-sided steel cladding was made of Evokin resin end laminate.
実施例2
実施例1と同じ積層体10組を成形圧力40 kg/d
、180″Cで閏分間積層成形後、加圧下で放冷しり分
間で160″Cに降温させ、加圧下で160°Cで鉛分
間積層成形した以外は実施例1と同様に処理して10枚
の積層板を得た。Example 2 Ten sets of the same laminates as in Example 1 were molded under a molding pressure of 40 kg/d.
After lamination molding at 180''C for a leap time, the temperature was lowered to 160''C for a minute under pressure, and lamination molding was performed at 160°C under pressure for a lead minute. Two laminates were obtained.
実施例3
実施例1と同じ積層体10 Miを成形圧力40 kq
/d、180℃でω分間積層成形後、加圧下で放冷しI
分間で160°Cに降温させ、加圧下で160°Cで田
分間積層成形した以外は実施例1と同様に処理して10
枚の蹟7v板を得た。Example 3 The same laminate 10 Mi as in Example 1 was molded at a pressure of 40 kq.
/d, after lamination molding at 180℃ for ω minutes, cool under pressure and I
The process was carried out in the same manner as in Example 1, except that the temperature was lowered to 160°C for 10 minutes, and Tamama laminated molding was performed at 160°C under pressure.
A total of 7V plates were obtained.
比較例
実施例1と同じ積層体10姐を成形圧力40 kg、f
d、180″Cで120分間積層成形した以外は実施例
1と同様に処理して10枚の積層板を得た。Comparative Example The same laminate as Example 1 was molded under a molding pressure of 40 kg, f.
d. Ten laminates were obtained in the same manner as in Example 1, except that laminate molding was carried out at 180''C for 120 minutes.
実施例1乃至3と比較例の積、W板の性能は第1表のよ
うである。The product of Examples 1 to 3 and the comparative example and the performance of the W plate are as shown in Table 1.
第1表
注 辛プレッシャークツカー試験
〔発明の効果〕
本発明は上述した如く構成されている。特許請求の範囲
第1項に記載した構成を有する積層板の製造方法におい
ては、積層板のバフツキが大巾に低下する効果を有して
いる。Note to Table 1: Spicy Pressure Cooker Test [Effects of the Invention] The present invention is constructed as described above. The method for manufacturing a laminate having the structure described in claim 1 has the effect of significantly reducing the buffiness of the laminate.
Claims (1)
層体多数を重ね、各積層体の上面及び又は下面に金属プ
レートを配設して積層成形するに際し、成形最高温度で
の所要成形時間を25〜50%短縮し、短縮分は成形最
高温度より10〜40℃低温に放冷後、その温度に保持
することを特徴とする積層板の製造方法。(1) When stacking a large number of laminates made of resin-impregnated base materials and metal foils between press hot platens and arranging metal plates on the top and/or bottom surfaces of each laminate for laminate molding, the required maximum molding temperature A method for manufacturing a laminate, characterized in that the molding time is shortened by 25 to 50%, and the shortened time is left to cool to a temperature 10 to 40°C lower than the maximum molding temperature, and then maintained at that temperature.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12645688A JPH01294017A (en) | 1988-05-23 | 1988-05-23 | Preparation of laminated sheet |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12645688A JPH01294017A (en) | 1988-05-23 | 1988-05-23 | Preparation of laminated sheet |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01294017A true JPH01294017A (en) | 1989-11-28 |
Family
ID=14935674
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP12645688A Pending JPH01294017A (en) | 1988-05-23 | 1988-05-23 | Preparation of laminated sheet |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01294017A (en) |
-
1988
- 1988-05-23 JP JP12645688A patent/JPH01294017A/en active Pending
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