JPH0355499B2 - - Google Patents
Info
- Publication number
- JPH0355499B2 JPH0355499B2 JP1566087A JP1566087A JPH0355499B2 JP H0355499 B2 JPH0355499 B2 JP H0355499B2 JP 1566087 A JP1566087 A JP 1566087A JP 1566087 A JP1566087 A JP 1566087A JP H0355499 B2 JPH0355499 B2 JP H0355499B2
- Authority
- JP
- Japan
- Prior art keywords
- resin
- flame
- retardant
- phenolic resin
- prepreg
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 229920005989 resin Polymers 0.000 claims description 26
- 239000011347 resin Substances 0.000 claims description 26
- 239000003063 flame retardant Substances 0.000 claims description 19
- 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 claims description 18
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 12
- 239000005011 phenolic resin Substances 0.000 claims description 10
- 229920001568 phenolic resin Polymers 0.000 claims description 9
- 238000001035 drying Methods 0.000 claims description 7
- 239000000463 material Substances 0.000 claims description 7
- LJCFOYOSGPHIOO-UHFFFAOYSA-N antimony pentoxide Chemical compound O=[Sb](=O)O[Sb](=O)=O LJCFOYOSGPHIOO-UHFFFAOYSA-N 0.000 claims description 6
- 239000004640 Melamine resin Substances 0.000 claims description 4
- 229920000877 Melamine resin Polymers 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 239000007787 solid Substances 0.000 claims description 2
- 230000000694 effects Effects 0.000 description 3
- 238000004080 punching Methods 0.000 description 3
- 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 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical class [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000003475 lamination Methods 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000011889 copper foil Substances 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical class C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 239000002655 kraft paper Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
Landscapes
- Reinforced Plastic Materials (AREA)
- Laminated Bodies (AREA)
Description
産業上の利用分野
本発明は、常温打抜き加工性、難燃性、耐熱
性、及び電気特性を高度に必要とする難燃性フエ
ノール樹脂積層板の製造法に関する。
最近民生機器に於いて、電気絶縁基板として難
燃性フエノール樹脂積層板を使用する率が増加す
る中で、高品質、且つ低価格の要求が益々高くな
つてきている。
高度な電気特性を持つ難燃性フエノール樹脂積
層板を得る為には、積層成形するプリプレグの作
製段階に於いて、基材への熱硬化性樹脂の含浸工
程を下塗りと上塗りの2度繰返す方法がある。従
来、フエノール樹脂初期縮合物とメラミン樹脂を
混合した下塗り樹脂を基材に含浸乾燥後、更に上
塗り樹脂として難燃剤及び難燃樹脂を配合した油
変性フエノール樹脂ワニスを含浸乾燥してプリプ
レグを作製していた。
発明が解決しようとする問題点
従来法に於いては難燃性を確保(UL−94V−
O)する為、下塗り樹脂中にメラミン樹脂を含有
させている。一方、上塗り樹脂中にブロム化エポ
キシ樹脂等の難燃樹脂とテトラブロモビスフエノ
ールA(TBA)、トリフエニルホスフエート
(TPP)等のブロム化合物やリン化合物等の難燃
剤が多量に含有されている為、得られた積層板の
層間密着性が劣り、常温打抜き性及び耐熱性が悪
くなり、更に高価になつている。
従つて、本発明は、常温打抜性、耐熱性が良好
で安価な難燃性フエノール樹脂積層板を提供する
事を目的とする。
問題点を解決するための手段
上記目的を達成するために、本発明は、フエノ
ール樹脂初期縮合物とメラミン樹脂の混合物に固
形分換算で3〜50重量%の五酸化アンチモン
(Sb2O5)ゾルを配合した下塗り樹脂を基材に含
浸乾燥せしめる第1工程、難燃樹脂を含有する油
変性フエノール樹脂を前記第1工程を経た基材に
含浸乾燥せしめる第2工程を経てプリプレグを作
製し、これを積層成形する事を特徴とするもので
ある。
作 用
本発明は、上記の特徴を有することにより、常
温打抜き加工性、難燃性、耐熱性、及び電気特性
を高度に必要とする難燃性フエノール樹脂積層板
が得られる。即ち、難燃性の向上の観点から見る
と、基材を下塗り樹脂で処理する段階が非常に重
要であり、効果がある。そこで、下塗りの樹脂中
に五酸化アンチモン(Sb2O5)ゾルを併用し鋭意
検討した結果、上塗り樹脂中の難燃剤を減らすこ
とが可能となり、前記目的を達成出来た。
但し、Sb2O5ゾルから下塗り樹脂中の3重量%
未満では上塗り樹脂中の難燃剤を減少出来る丈の
効果は見られなかつた。又、Sb2O5ゾルが下塗り
樹脂中の50重量%を越えると積層板が不透明にな
り品質上問題がある。好ましい量としては15〜30
重量%である。
実施例
次に、本発明の実施例を比較例、従来例と共に
説明する。
第1表に示す配合割合(重量%)の下塗り樹脂
を11ミルスのクラフト紙に樹脂量10〜15重量%に
なるよう含浸乾燥した後、更に上塗り樹脂を含浸
乾燥せしめる事によつて樹脂量48〜51重量%のプ
リプレグを製造した。このプリプレグを所定枚数
とプリプレグの片側表面に35μ厚銅箔を一体に積
層し、160℃、100Kg/cm2の加熱、加圧下で成形し
1.6mm厚の銅張り積層板を得た。
INDUSTRIAL APPLICATION FIELD The present invention relates to a method for producing a flame-retardant phenolic resin laminate that requires high room-temperature punching workability, flame retardancy, heat resistance, and electrical properties. Recently, as the use of flame-retardant phenolic resin laminates as electric insulating substrates in consumer electronics has been increasing, the demand for high quality and low cost has become higher and higher. In order to obtain flame-retardant phenolic resin laminates with advanced electrical properties, the process of impregnating the base material with thermosetting resin is repeated twice: undercoating and topcoating, during the prepreg production stage for lamination molding. There is. Conventionally, a prepreg is produced by impregnating and drying a base material with an undercoat resin that is a mixture of a phenolic resin initial condensate and a melamine resin, and then impregnating and drying an oil-modified phenolic resin varnish containing a flame retardant and a flame retardant resin as a top coat resin. was. Problems to be solved by the invention Conventional methods ensure flame retardancy (UL-94V-
O), melamine resin is contained in the undercoat resin. On the other hand, the top coat resin contains large amounts of flame retardant resins such as brominated epoxy resins and flame retardants such as bromine compounds such as tetrabromobisphenol A (TBA) and triphenyl phosphate (TPP), and phosphorus compounds. Therefore, the resulting laminate has poor interlayer adhesion, poor punchability at room temperature and heat resistance, and is more expensive. Therefore, an object of the present invention is to provide an inexpensive flame-retardant phenolic resin laminate that has good room-temperature punchability and heat resistance. Means for Solving the Problems In order to achieve the above object, the present invention provides a mixture of a phenolic resin initial condensate and a melamine resin with 3 to 50% by weight of antimony pentoxide (Sb 2 O 5 in terms of solid content). A prepreg is produced through a first step of impregnating and drying an undercoat resin containing a sol into a base material, a second step of impregnating and drying an oil-modified phenol resin containing a flame retardant resin into the base material that has undergone the first step, This is characterized by lamination molding. Effects By having the above-mentioned characteristics, the present invention provides a flame-retardant phenolic resin laminate that requires high room-temperature punching workability, flame retardancy, heat resistance, and electrical properties. That is, from the viewpoint of improving flame retardancy, the step of treating the base material with the undercoat resin is very important and effective. Therefore, as a result of intensive studies using antimony pentoxide (Sb 2 O 5 ) sol in the undercoat resin, it became possible to reduce the amount of flame retardant in the topcoat resin, and the above objective was achieved. However, from Sb 2 O 5 sol to 3% by weight in the undercoat resin.
When the length was less than 100%, no effect of reducing the flame retardant in the top coat resin was observed. Furthermore, if the Sb 2 O 5 sol exceeds 50% by weight in the undercoat resin, the laminate becomes opaque, which poses a quality problem. The preferred amount is 15-30
Weight%. Examples Next, examples of the present invention will be described together with comparative examples and conventional examples. After impregnating and drying 11 mils kraft paper with the undercoat resin in the proportions (wt%) shown in Table 1 to a resin content of 10 to 15% by weight, further impregnating and drying the topcoat resin resulted in a resin content of 48%. ~51 wt% prepreg was produced. A predetermined number of sheets of this prepreg and 35 μ thick copper foil are laminated together on one surface of the prepreg, and molded under heat and pressure at 160℃ and 100Kg/cm 2 .
A copper-clad laminate with a thickness of 1.6 mm was obtained.
【表】
尚、第1表で難燃樹脂は、ブロム化エポキシ樹
脂にトリフエニルホスフエートを溶解混合したも
のである。
上記実施例並びに比較例、従来例で得られた銅
張り積層板の特性試験結果を第2表に示す。[Table] In Table 1, the flame-retardant resin is a mixture of brominated epoxy resin and triphenyl phosphate. Table 2 shows the characteristics test results of the copper-clad laminates obtained in the above Examples, Comparative Examples, and Conventional Examples.
【表】【table】
【表】
発明の効果
上述したように、本発明によれば、第1表及び
第2表からわかる様に難燃性を保持しながら上塗
り樹脂中の難燃剤と共に難燃樹脂をも使用量を減
少出来、油変性フエノール樹脂量を増加する事が
可能となつたので、耐熱性、打抜き加工性の向上
が図れた。また、下塗り樹脂中にSb2O5ゾルを用
いる事により高価なブロム、リン系難燃剤、難燃
樹脂が減少出来る為積層板のコストダウンが出
来、工業的価値は極めて大なるものである。[Table] Effects of the Invention As described above, according to the present invention, as can be seen from Tables 1 and 2, the amount of flame retardant resin used together with the flame retardant in the top coat resin can be reduced while maintaining flame retardancy. Since it became possible to increase the amount of oil-modified phenolic resin, heat resistance and punching workability were improved. In addition, by using Sb 2 O 5 sol in the undercoat resin, the amount of expensive bromine, phosphorus flame retardant, and flame retardant resin can be reduced, so the cost of the laminate can be reduced, and the industrial value is extremely large.
Claims (1)
混合物に固形分換算で3〜50重量%の五酸化アン
チモン(Sb2O5)ゾルを配合した下塗り樹脂を基
材に含浸乾燥せしめる第1工程、難燃樹脂を含有
する油変性フエノール樹脂を前記第1工程を経た
基材に含浸乾燥せしめる第2工程を経てプリプレ
グを作製し、このプリプレグを積層成形する事を
特徴とする難燃性フエノール樹脂積層板の製造
法。1. The first step is to impregnate and dry the base material with an undercoat resin, which is a mixture of a phenolic resin initial condensate and a melamine resin mixed with antimony pentoxide (Sb 2 O 5 ) sol of 3 to 50% by weight in terms of solid content, flame retardant. A flame-retardant phenolic resin laminate characterized in that a prepreg is produced through a second step of impregnating and drying an oil-modified phenolic resin containing resin into the base material that has passed through the first step, and this prepreg is laminated and molded. Manufacturing method.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1566087A JPS63183939A (en) | 1987-01-26 | 1987-01-26 | Production of laminated flame-retardant phenolic resin board |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1566087A JPS63183939A (en) | 1987-01-26 | 1987-01-26 | Production of laminated flame-retardant phenolic resin board |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS63183939A JPS63183939A (en) | 1988-07-29 |
| JPH0355499B2 true JPH0355499B2 (en) | 1991-08-23 |
Family
ID=11894892
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1566087A Granted JPS63183939A (en) | 1987-01-26 | 1987-01-26 | Production of laminated flame-retardant phenolic resin board |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS63183939A (en) |
-
1987
- 1987-01-26 JP JP1566087A patent/JPS63183939A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS63183939A (en) | 1988-07-29 |
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