JPH08165454A - Heat-resistant moistureproof insulation coating and production of insulated electronic part - Google Patents
Heat-resistant moistureproof insulation coating and production of insulated electronic partInfo
- Publication number
- JPH08165454A JPH08165454A JP30878194A JP30878194A JPH08165454A JP H08165454 A JPH08165454 A JP H08165454A JP 30878194 A JP30878194 A JP 30878194A JP 30878194 A JP30878194 A JP 30878194A JP H08165454 A JPH08165454 A JP H08165454A
- Authority
- JP
- Japan
- Prior art keywords
- parts
- heat
- weight
- resistant
- electronic part
- 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
- 238000000576 coating method Methods 0.000 title claims abstract description 23
- 239000011248 coating agent Substances 0.000 title claims abstract description 22
- 238000009413 insulation Methods 0.000 title claims abstract description 11
- 238000004519 manufacturing process Methods 0.000 title claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 16
- 239000005062 Polybutadiene Substances 0.000 claims abstract description 10
- 229920002857 polybutadiene Polymers 0.000 claims abstract description 10
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims abstract description 9
- 239000002904 solvent Substances 0.000 claims abstract description 8
- 229920001228 polyisocyanate Polymers 0.000 claims abstract description 5
- 239000005056 polyisocyanate Substances 0.000 claims abstract description 5
- 229920000642 polymer Polymers 0.000 claims abstract description 3
- 239000003973 paint Substances 0.000 claims description 7
- 239000000463 material Substances 0.000 claims description 5
- 238000001035 drying Methods 0.000 claims description 4
- 239000008199 coating composition Substances 0.000 claims description 3
- 230000006866 deterioration Effects 0.000 abstract description 4
- 238000000034 method Methods 0.000 abstract description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
- 230000000052 comparative effect Effects 0.000 description 6
- 239000002966 varnish Substances 0.000 description 6
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- -1 copper and solder Chemical class 0.000 description 3
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000008096 xylene Substances 0.000 description 3
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-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
- 239000013032 Hydrocarbon resin Substances 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical class CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
- 125000002723 alicyclic group Chemical group 0.000 description 2
- FPCJKVGGYOAWIZ-UHFFFAOYSA-N butan-1-ol;titanium Chemical group [Ti].CCCCO.CCCCO.CCCCO.CCCCO FPCJKVGGYOAWIZ-UHFFFAOYSA-N 0.000 description 2
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
- 229910001873 dinitrogen Inorganic materials 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- 229920006270 hydrocarbon resin Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229930195734 saturated hydrocarbon Natural products 0.000 description 2
- 229920002050 silicone resin Polymers 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 2
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
- YCIGYTFKOXGYTA-UHFFFAOYSA-N 4-(3-cyanopropyldiazenyl)butanenitrile Chemical compound N#CCCCN=NCCCC#N YCIGYTFKOXGYTA-UHFFFAOYSA-N 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- NBICYCZLCAMSBG-UHFFFAOYSA-L [Co+2].CCCCCC=CC([O-])=O.CCCCCC=CC([O-])=O Chemical compound [Co+2].CCCCCC=CC([O-])=O.CCCCCC=CC([O-])=O NBICYCZLCAMSBG-UHFFFAOYSA-L 0.000 description 1
- COYJIMCVCRLOIW-UHFFFAOYSA-L [Mn+2].CCCCCC=CC([O-])=O.CCCCCC=CC([O-])=O Chemical compound [Mn+2].CCCCCC=CC([O-])=O.CCCCCC=CC([O-])=O COYJIMCVCRLOIW-UHFFFAOYSA-L 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000005456 alcohol based solvent Substances 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000003990 capacitor Substances 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000003759 ester based solvent Substances 0.000 description 1
- XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical group CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 235000010985 glycerol esters of wood rosin Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- SGGOJYZMTYGPCH-UHFFFAOYSA-L manganese(2+);naphthalene-2-carboxylate Chemical compound [Mn+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 SGGOJYZMTYGPCH-UHFFFAOYSA-L 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical class OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 229910000679 solder Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 239000005028 tinplate Substances 0.000 description 1
- 238000005406 washing Methods 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
- H05K3/22—Secondary treatment of printed circuits
- H05K3/28—Applying non-metallic protective coatings
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Polyurethanes Or Polyureas (AREA)
- Paints Or Removers (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、電子部品の絶縁に適し
た耐熱性に優れた防湿絶縁塗料および絶縁処理された電
子部品の製造法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a moisture-proof insulating coating having excellent heat resistance suitable for insulating electronic parts and a method for producing an electronic part subjected to an insulation treatment.
【0002】[0002]
【従来の技術】電気機器は年々小型軽量化および多機能
化の傾向にあり、これを制御する各種電気機器に搭載し
た実装回路板は、湿気、塵埃、ガス等から保護する目的
で絶縁処理が行われている。この絶縁処理法には、アク
リル系樹脂、シリコーン系樹脂、特公平4−26354
号公報に記載のウレタン系樹脂等の塗料による保護コー
ティング処理が広く採用されている。このような実装回
路板は、過酷な環境下、特に高湿度下で使用され、例え
ば洗濯機、自動車等の機器に搭載されて使用されてい
る。しかしながら、前記アクリル系樹脂の塗料は、耐熱
性が80〜100℃であり、加熱劣化後の可とう性が失
われ、耐熱性が要求される用途での使用が限定されてい
た。一方、シリコーン系樹脂の塗料は、耐熱性に優れ、
加熱劣化後の可とう性は良いが材料価格が高く、かつ塗
料に皮張り、ゲル化等が発生し作業性に問題があった。
さらに、特公平4−26354号公報記載のウレタン系
樹脂の塗料は、耐熱性と作業性に優れているが、銅、ハ
ンダ等の金属との密着性に劣り、信頼性に問題があっ
た。2. Description of the Related Art Electric equipment tends to be smaller and lighter and has more and more functions year by year, and mounted circuit boards mounted on various electric equipments for controlling the electric equipment have insulation treatment for the purpose of protection from moisture, dust, gas and the like. Has been done. This insulation treatment method includes acrylic resin, silicone resin and Japanese Patent Publication No. 26354.
The protective coating treatment with a paint such as urethane resin described in Japanese Patent Publication is widely adopted. Such a mounting circuit board is used in a harsh environment, especially under high humidity, and is mounted and used in equipment such as a washing machine and an automobile. However, the acrylic resin coating material has a heat resistance of 80 to 100 ° C., loses its flexibility after heat deterioration, and is limited in use in applications requiring heat resistance. On the other hand, silicone resin paints have excellent heat resistance,
The flexibility after heat deterioration was good, but the material cost was high, and there was a problem in workability because the paint crusted and gelled.
Further, the urethane resin coating described in JP-B-4-26354 has excellent heat resistance and workability, but has poor adhesion to metals such as copper and solder, and has a problem in reliability.
【0003】[0003]
【発明が解決しようとする課題】本発明は、このような
従来技術の問題点を解決し、防湿絶縁等に適し、耐熱性
に優れた耐熱性防湿絶縁塗料および絶縁処理された電子
部品の製造法を提供するものである。SUMMARY OF THE INVENTION The present invention solves the problems of the prior art and is suitable for moisture-proof insulation and the like, and is capable of producing a heat-resistant moisture-proof insulation coating excellent in heat resistance and an insulation-treated electronic component. It provides the law.
【0004】[0004]
【課題を解決するための手段】本発明は、(a)水酸基
含有ポリブタジエン100重量部、(b)水酸基含有水
素添加ポリブタジエン30〜300重量部および(c)
ポリイソシアネートを、(a)および(b)成分の水酸
基1モルに対し、イソシアネート基が0.7〜1.5モ
ルの範囲となる割合で反応させて得られるポリマー、
(d)粘着付与剤10〜100重量部ならびに(e)溶
剤を含有してなる耐熱性防湿絶縁塗料およびこの塗料を
電子部品に塗布し、乾燥する絶縁処理された電子部品の
製造法に関する。The present invention comprises (a) 100 parts by weight of hydroxyl group-containing polybutadiene, (b) 30 to 300 parts by weight of hydroxyl group-containing hydrogenated polybutadiene, and (c).
A polymer obtained by reacting polyisocyanate at a ratio such that the isocyanate group is in the range of 0.7 to 1.5 mol, relative to 1 mol of the hydroxyl group of the components (a) and (b),
The present invention relates to a heat-resistant and moisture-proof insulating coating containing 10 to 100 parts by weight of a tackifier and (e) a solvent, and a method for producing an insulating-processed electronic component by applying the coating to an electronic component and drying.
【0005】本発明に用いられる(a)水酸基含有ポリ
ブタジエンは、分子内または分子末端に水酸基を有し、
塗膜の可とう性および作業性から数平均分子量は好まし
くは、300〜1000、より好ましくは500〜50
00の範囲とされる。この市販品としては、例えばG−
1000、G−2000(日本曹達社製)が挙げられ
る。The (a) hydroxyl group-containing polybutadiene used in the present invention has a hydroxyl group in the molecule or at the terminal of the molecule,
From the flexibility and workability of the coating film, the number average molecular weight is preferably 300 to 1000, more preferably 500 to 50.
The range is 00. Examples of this commercial product include G-
1000, G-2000 (made by Nippon Soda Co., Ltd.) are mentioned.
【0006】本発明に用いられる(b)水酸基含有水素
添加ポリブタジエンは、分子内または分子末端に水酸基
を有し、塗膜の可とう性から水素添加率が好ましくは9
0%以上で、塗膜の可とう性および作業性から数平均分
子量は好ましくは300〜10000、より好ましくは
500〜5000の範囲とされる。この市販品として
は、例えばGI−2000(日本曹達社製)が挙げられ
る。The (b) hydroxyl group-containing hydrogenated polybutadiene used in the present invention has a hydroxyl group in the molecule or at the terminal of the molecule, and preferably has a hydrogenation rate of 9 from the flexibility of the coating film.
When it is 0% or more, the number average molecular weight is preferably in the range of 300 to 10,000, more preferably 500 to 5,000 in view of flexibility and workability of the coating film. Examples of this commercially available product include GI-2000 (manufactured by Nippon Soda Co., Ltd.).
【0007】本発明に用いられる(c)ポリイソシアネ
ートは、トリレンジイソシアネート、ジフェニルメタン
ジイソシアネート、ヘキサメチレンジイソシアネート、
これらのトリメチロールプロパン付加物、ペンタエリス
リトールの付加物等であり、1分子中に2個以上のイソ
シアネート基を有するイソシアネート化合物である。The (c) polyisocyanate used in the present invention is tolylene diisocyanate, diphenylmethane diisocyanate, hexamethylene diisocyanate,
These trimethylolpropane adducts, pentaerythritol adducts, and the like are isocyanate compounds having two or more isocyanate groups in one molecule.
【0008】本発明に用いられる(d)粘着付与剤は、
溶剤に溶解しやすく、常温で固形の軟化点が好ましくは
50〜180℃、より好ましくは60〜170℃の水素
添加ロジン系樹脂、脂環族系飽和炭化水素樹脂等が挙げ
られる。The tackifier (d) used in the present invention is
Examples thereof include hydrogenated rosin-based resins and alicyclic saturated hydrocarbon resins which are easily dissolved in a solvent and have a solid softening point at room temperature of preferably 50 to 180 ° C, more preferably 60 to 170 ° C.
【0009】本発明に用いられる(e)溶剤は、アセト
ン、メチルエチルケトン等のケトン系溶剤、トルエン、
キシレン等の芳香族系溶剤、酢酸エチル、酢酸ブチル等
のエステル系溶剤、エチルアルコール、ブチルアルコー
ル等のアルコール系溶剤、ミネラルターペン、ナフサ等
の石油系溶剤などである。The solvent (e) used in the present invention is a ketone solvent such as acetone or methyl ethyl ketone, toluene,
Examples thereof include aromatic solvents such as xylene, ester solvents such as ethyl acetate and butyl acetate, alcohol solvents such as ethyl alcohol and butyl alcohol, petroleum solvents such as mineral terpenes and naphtha.
【0010】本発明の(a)、(b)および(c)の配
合割合は、(a)成分100重量部に対し、(b)成分
は30〜300重量部の範囲とされる。(b)成分が3
0重量部未満の場合は熱劣化後の塗膜の可とう性の変化
が大きく、300重量部を超えると乾燥性が悪くなる。
(c)成分のポリイソシアネートは、(a)および
(b)成分の水酸基1モルに対しイソシアネート基が
0.7〜1.5モルの範囲となる割合で(a)および
(b)成分と反応させる。イソシアネート基が1.5モ
ルを超えるとイソシアネート基が残存し、塗料の安定性
上好ましくなく、イソシアネート基が0.7モル未満の
場合は反応物の分子量が大きくならない。(a)、
(b)および(c)成分は同時に反応させても、2成分
を先に反応させついで他の成分を反応させてもよい。The blending ratio of (a), (b) and (c) of the present invention is in the range of 30 to 300 parts by weight of the component (b) with respect to 100 parts by weight of the component (a). (B) component is 3
When the amount is less than 0 parts by weight, the flexibility of the coating film after heat deterioration is large, and when it exceeds 300 parts by weight, the drying property is deteriorated.
The polyisocyanate as the component (c) reacts with the components (a) and (b) at a ratio such that the isocyanate group is in the range of 0.7 to 1.5 mol with respect to 1 mol of the hydroxyl group as the components (a) and (b). Let When the isocyanate group exceeds 1.5 mol, the isocyanate group remains, which is not preferable from the viewpoint of stability of the coating material. When the isocyanate group is less than 0.7 mol, the molecular weight of the reaction product does not increase. (A),
The components (b) and (c) may be reacted at the same time, or the two components may be reacted first and then the other components.
【0011】(d)粘着仕上剤の配合量は、(a)、
(b)および(c)成分の反応物100重量部に対し、
10〜100重量部の範囲とされる。(d)成分が10
重量部未満の場合は密着性に劣り、100重量部を超え
ると塗膜の可とう性、防湿性が低下する。(D) The amount of the adhesive finish compounded is (a),
With respect to 100 parts by weight of the reaction products of the components (b) and (c),
The range is 10 to 100 parts by weight. (D) component is 10
When it is less than 100 parts by weight, the adhesion is poor, and when it exceeds 100 parts by weight, the flexibility and moisture resistance of the coating film are deteriorated.
【0012】(e)溶剤の配合量は、作業性に関連する
塗料の粘度に応じて決められるが、通常、耐熱性防湿絶
縁塗料に対して20〜80重量%の割合とされる。ま
た、本発明の塗料には、微粉末酸化けい素、酸化マグネ
シウム、炭酸カルシウム等のフィラーが使用できる。ま
た、乾燥性を向上させるためにナフテン酸マンガン、オ
クテン酸マンガン、ナフテン酸コバルト、オクテン酸コ
バルト等の有機酸金属塩、ターシャリーブチルチタネー
ト、ターシャリーブチルチタネートとアセト酢酸エチル
との反応物などが使用できる。The blending amount of the solvent (e) is determined according to the viscosity of the coating composition which is related to workability, but is usually 20 to 80% by weight with respect to the heat resistant moistureproof insulating coating composition. In addition, fillers such as finely divided silicon oxide, magnesium oxide and calcium carbonate can be used in the coating material of the present invention. Further, in order to improve the drying property, manganese naphthenate, manganese octenoate, cobalt naphthenate, organic acid metal salts such as cobalt octenoate, tertiary butyl titanate, a reaction product of tertiary butyl titanate and ethyl acetoacetate, etc. Can be used.
【0013】本発明になる耐熱性防湿絶縁塗料を用いて
絶縁されたマイコン、トランジスタ、コンデンサ等、こ
れらを搭載した実装回路板などの電子部品が製造される
が、その製造法としては、一般に知られている浸漬法、
ハケ塗り法、スプレー法等によってこの塗料を上記電子
部品に塗布し、乾燥すればよい。Electronic components such as a microcomputer, a transistor, and a capacitor, which are insulated by using the heat-resistant and moisture-proof insulating paint according to the present invention, such as a mounting circuit board on which the components are mounted, are manufactured by a generally known method. Dipping method,
The paint may be applied to the electronic component by a brush coating method, a spray method, or the like and dried.
【0014】以下に本発明を実施例により説明するが、
本発明はこれらに制限されるものではない。以下、
「部」として表わしたものは重量部を示す。 比較例1 メタクリル酸ブチル214部、アクリル酸ブチル25
部、トルエン150部を1リットルの四つ口フラスコに
加え、窒素ガスを通しながら90℃まで昇温し保温し
た。これにメタクリル酸ブチル200部、アクリル酸ブ
チル21部、アゾビスブチロニトリル3部を混合溶解し
た溶液を2時間で滴下しながら重合を進めた。その後、
110℃に昇温し、2時間保温して重合を完了させた後
冷却し50℃になったらトルエン200部を加え10分
間撹拌し均一溶液ワニスAを得た。The present invention will be described below with reference to examples.
The present invention is not limited to these. Less than,
Those expressed as "parts" indicate parts by weight. Comparative Example 1 214 parts of butyl methacrylate and 25 parts of butyl acrylate
And 150 parts of toluene were added to a 1-liter four-necked flask, and the temperature was raised to 90 ° C. while maintaining the temperature while passing nitrogen gas. Polymerization was carried out while dropwise adding a solution in which 200 parts of butyl methacrylate, 21 parts of butyl acrylate, and 3 parts of azobisbutyronitrile were dissolved for 2 hours. afterwards,
After the temperature was raised to 110 ° C., the temperature was kept for 2 hours to complete the polymerization and then cooled, and when the temperature reached 50 ° C., 200 parts of toluene was added and stirred for 10 minutes to obtain a uniform solution varnish A.
【0015】比較例2 1リットルの四つ口フラスコにトリメチロールプロパン
45部、トリレンジイソシアネート174部、酢酸ブチ
ル219部を加え、窒素ガス雰囲気下で撹拌し、80℃
で2時間反応させた。次いで、G−1000(日本曹達
社製商品名、水酸基含有ポリブタジエン、数平均分子量
1400)281部と酢酸ブチル281部を混合溶解し
た溶液を約1時間で滴下し、その後80℃で2時間反応
させワニスBを得た。Comparative Example 2 45 parts of trimethylolpropane, 174 parts of tolylene diisocyanate and 219 parts of butyl acetate were added to a 1 liter four-necked flask, and the mixture was stirred under a nitrogen gas atmosphere at 80 ° C.
And reacted for 2 hours. Then, a solution prepared by mixing and dissolving 281 parts of G-1000 (trade name of Nippon Soda Co., Ltd., hydroxyl group-containing polybutadiene, number average molecular weight 1400) and 281 parts of butyl acetate was added dropwise in about 1 hour, and then reacted at 80 ° C. for 2 hours. Varnish B was obtained.
【0016】比較例3 1リットルの四つ口フラスコにGI−2000(日本曹
達社製商品名、水酸基含有水素添加ポリブタジエン、数
平均分子量2100)280部、キシレン280部、比
較例2で得たワニスB460部を混合撹拌し70℃で3
時間反応させた。このときのイソシアネート基のモル数
は水酸基1モルに対して、1.1モルであった。その
後、50℃に合成温度を下げエチルアルコール100部
を加え50℃で1時間反応させワニスCを得た。Comparative Example 3 280 parts of GI-2000 (trade name of Nippon Soda Co., Ltd., hydroxylated hydrogenated polybutadiene, number average molecular weight 2100), 280 parts of xylene, and 280 parts of xylene in a 1 liter four-necked flask, the varnish obtained in Comparative Example 2 Mix 460 parts of B and stir at 70 ° C for 3
Allowed to react for hours. At this time, the number of moles of isocyanate groups was 1.1 moles per 1 mole of hydroxyl groups. Then, the synthesis temperature was lowered to 50 ° C., 100 parts of ethyl alcohol was added, and the mixture was reacted at 50 ° C. for 1 hour to obtain a varnish C.
【0017】実施例1 1リットルの四つ口フラスコに比較例3で得たワニスC
250部、水素添加ロジン系樹脂(軟化点80℃、荒川
化学工業社製商品名、エステルガムHP)40部、トル
エン210部を加え、室温で撹拌し均一溶液ワニスDを
得た。Example 1 Varnish C obtained in Comparative Example 3 in a 1-liter four-necked flask
250 parts of hydrogenated rosin resin (softening point 80 ° C., trade name of Arakawa Chemical Industry Co., Ltd., ester gum HP) 40 parts and 210 parts of toluene were added and stirred at room temperature to obtain a uniform solution varnish D.
【0018】実施例2 1リットルの四つ口フラスコに比較例3で得たワニスC
250部、脂環族系飽和炭化水素樹脂(軟化点125
℃、荒川化学工業社製商品名、アルコンP−125)4
0部、トルエン210部を加え、室温で撹拌し均一溶液
ワニスEを得た。Example 2 Varnish C obtained in Comparative Example 3 in a 1-liter four-necked flask
250 parts, alicyclic saturated hydrocarbon resin (softening point 125
℃, trade name of Arakawa Chemical Industry Co., Ltd., Alcon P-125) 4
0 parts and 210 parts of toluene were added and stirred at room temperature to obtain a uniform solution varnish E.
【0019】以上で得たワニスA〜Eを鉛筆硬度および
屈曲性試験用としてブリキ板(50×180×0.25
mm)に、密着性試験用として銅板(50×100×1.
6mm)に各々塗布し、80℃で2時間乾燥し20μm
の塗膜を作成した。ついで、この塗膜を125℃の恒温
槽に放置し、各時間毎に鉛筆硬度、屈曲性および銅との
密着性を測定した。結果を表1に示す。The varnishes A to E obtained above were used as a tin plate (50 × 180 × 0.25) for pencil hardness and flexibility tests.
mm) and a copper plate (50 × 100 × 1.
6 mm) and dried at 80 ° C for 2 hours to 20 μm
A coating film of Then, this coating film was left in a constant temperature bath at 125 ° C., and the pencil hardness, the flexibility and the adhesion to copper were measured every time. The results are shown in Table 1.
【0020】[0020]
【表1】 [Table 1]
【0021】[0021]
【発明の効果】本発明の耐熱性防湿絶縁塗料の塗膜は、
高温で加熱劣化しても可とう性および金属との密着性が
低下しないことから耐熱性に優れ、これによって高い信
頼性の絶縁処理された電子部品を得ることができる。The coating film of the heat-resistant and moisture-proof insulating paint of the present invention is
Since the flexibility and the adhesiveness to a metal do not deteriorate even if it is deteriorated by heating at a high temperature, the heat resistance is excellent, and thus a highly reliable insulation-treated electronic component can be obtained.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 // C08G 18/62 NFC 18/69 NFC ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification number Office reference number FI technical display location // C08G 18/62 NFC 18/69 NFC
Claims (3)
重量部、(b)水酸基含有水素添加ポリブタジエン30
〜300重量部および(c)ポリイソシアネートを、
(a)および(b)成分の水酸基1モルに対し、イソシ
アネート基が0.7〜1.5モルの範囲となる割合で反
応させて得られるポリマー、(d)粘着付与剤10〜1
00重量部ならびに(e)溶剤を含有してなる耐熱性防
湿絶縁塗料。1. (a) Hydroxyl group-containing polybutadiene 100
Parts by weight, (b) hydroxyl group-containing hydrogenated polybutadiene 30
~ 300 parts by weight and (c) polyisocyanate,
Polymers obtained by reacting isocyanate groups in a ratio of 0.7 to 1.5 moles with respect to 1 mole of hydroxyl groups of components (a) and (b), and (d) tackifiers 10 to 1.
A heat-resistant and moisture-proof insulating coating material containing 00 parts by weight and (e) a solvent.
範囲である請求項1記載の耐熱性防湿絶縁塗料。2. The heat-resistant moisture-proof insulating coating composition according to claim 1, wherein the tackifier has a softening point in the range of 50 to 180 ° C.
電子部品に塗布し、乾燥する絶縁処理された電子部品の
製造法。3. The heat-resistant and moisture-proof insulating paint according to claim 1,
A method of manufacturing electronic components that have been subjected to insulation treatment by applying to electronic components and drying.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP30878194A JPH08165454A (en) | 1994-12-13 | 1994-12-13 | Heat-resistant moistureproof insulation coating and production of insulated electronic part |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP30878194A JPH08165454A (en) | 1994-12-13 | 1994-12-13 | Heat-resistant moistureproof insulation coating and production of insulated electronic part |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH08165454A true JPH08165454A (en) | 1996-06-25 |
Family
ID=17985234
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP30878194A Pending JPH08165454A (en) | 1994-12-13 | 1994-12-13 | Heat-resistant moistureproof insulation coating and production of insulated electronic part |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH08165454A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0994140A1 (en) * | 1998-10-15 | 2000-04-19 | Ajinomoto Co., Inc. | Curable resin composition for coating flexible circuits |
JP2000186248A (en) * | 1998-10-15 | 2000-07-04 | Ajinomoto Co Inc | Resin composition for flexible circuit over-coating |
JP2020169302A (en) * | 2019-04-05 | 2020-10-15 | 日東シンコー株式会社 | Moisture-proof coating composition |
-
1994
- 1994-12-13 JP JP30878194A patent/JPH08165454A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0994140A1 (en) * | 1998-10-15 | 2000-04-19 | Ajinomoto Co., Inc. | Curable resin composition for coating flexible circuits |
JP2000186248A (en) * | 1998-10-15 | 2000-07-04 | Ajinomoto Co Inc | Resin composition for flexible circuit over-coating |
JP2020169302A (en) * | 2019-04-05 | 2020-10-15 | 日東シンコー株式会社 | Moisture-proof coating composition |
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