JPH0312260A - Powder painting method - Google Patents
Powder painting methodInfo
- Publication number
- JPH0312260A JPH0312260A JP1144002A JP14400289A JPH0312260A JP H0312260 A JPH0312260 A JP H0312260A JP 1144002 A JP1144002 A JP 1144002A JP 14400289 A JP14400289 A JP 14400289A JP H0312260 A JPH0312260 A JP H0312260A
- Authority
- JP
- Japan
- Prior art keywords
- phenol resin
- resin
- resistance
- polybutadiene
- coating
- 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
- 238000000034 method Methods 0.000 title claims abstract description 13
- 238000010433 powder painting Methods 0.000 title abstract 2
- 238000000576 coating method Methods 0.000 claims abstract description 37
- 239000011248 coating agent Substances 0.000 claims abstract description 29
- 239000000843 powder Substances 0.000 claims abstract description 23
- 239000005011 phenolic resin Substances 0.000 claims abstract description 16
- 229920002857 polybutadiene Polymers 0.000 claims abstract description 14
- 239000005062 Polybutadiene Substances 0.000 claims abstract description 12
- 229920001568 phenolic resin Polymers 0.000 claims description 8
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 5
- 238000010422 painting Methods 0.000 claims description 4
- 239000000463 material Substances 0.000 abstract description 20
- 239000002904 solvent Substances 0.000 abstract description 11
- 239000003973 paint Substances 0.000 abstract description 4
- 229920003986 novolac Polymers 0.000 abstract description 3
- 229920003987 resole Polymers 0.000 abstract description 3
- 239000004215 Carbon black (E152) Substances 0.000 abstract description 2
- 125000003700 epoxy group Chemical group 0.000 abstract description 2
- 229930195733 hydrocarbon Natural products 0.000 abstract description 2
- 150000002430 hydrocarbons Chemical class 0.000 abstract description 2
- 239000011247 coating layer Substances 0.000 abstract 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 12
- 229920005989 resin Polymers 0.000 description 9
- 239000011347 resin Substances 0.000 description 9
- 239000010408 film Substances 0.000 description 8
- 239000003054 catalyst Substances 0.000 description 7
- -1 dip Substances 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- 229920002050 silicone resin Polymers 0.000 description 5
- 238000011156 evaluation Methods 0.000 description 4
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 4
- 150000002989 phenols Chemical class 0.000 description 4
- 239000011134 resol-type phenolic resin Substances 0.000 description 4
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 4
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-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
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 3
- 150000001342 alkaline earth metals Chemical class 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 3
- 230000018044 dehydration Effects 0.000 description 3
- 238000006297 dehydration reaction Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000035939 shock Effects 0.000 description 3
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical group CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 239000004312 hexamethylene tetramine Substances 0.000 description 2
- 235000010299 hexamethylene tetramine Nutrition 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 238000007665 sagging Methods 0.000 description 2
- 230000035882 stress Effects 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 1
- 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
- IGFHQQFPSIBGKE-UHFFFAOYSA-N 4-nonylphenol Chemical compound CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- NTDQQZYCCIDJRK-UHFFFAOYSA-N 4-octylphenol Chemical compound CCCCCCCCC1=CC=C(O)C=C1 NTDQQZYCCIDJRK-UHFFFAOYSA-N 0.000 description 1
- QHPQWRBYOIRBIT-UHFFFAOYSA-N 4-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C=C1 QHPQWRBYOIRBIT-UHFFFAOYSA-N 0.000 description 1
- 229920001342 Bakelite® Polymers 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229920003261 Durez Polymers 0.000 description 1
- 241000156978 Erebia Species 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000005456 alcohol based solvent Substances 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 239000004637 bakelite Substances 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- YXVFYQXJAXKLAK-UHFFFAOYSA-N biphenyl-4-ol Chemical compound C1=CC(O)=CC=C1C1=CC=CC=C1 YXVFYQXJAXKLAK-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000003990 capacitor Substances 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000003985 ceramic capacitor Substances 0.000 description 1
- 239000007809 chemical reaction catalyst Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 238000005538 encapsulation Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003759 ester based solvent Substances 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000005243 fluidization Methods 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000012778 molding material Substances 0.000 description 1
- IUBMRJVNZLQSHU-FDJBSCRHSA-N monate-a Chemical compound C[C@H](O)[C@H](C)[C@@H]1O[C@H]1C[C@@H]1[C@@H](O)[C@@H](O)[C@H](C\C(C)=C\C(O)=O)OC1 IUBMRJVNZLQSHU-FDJBSCRHSA-N 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000013034 phenoxy resin Substances 0.000 description 1
- 229920006287 phenoxy resin Polymers 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- DVQHRBFGRZHMSR-UHFFFAOYSA-N sodium methyl 2,2-dimethyl-4,6-dioxo-5-(N-prop-2-enoxy-C-propylcarbonimidoyl)cyclohexane-1-carboxylate Chemical compound [Na+].C=CCON=C(CCC)[C-]1C(=O)CC(C)(C)C(C(=O)OC)C1=O DVQHRBFGRZHMSR-UHFFFAOYSA-N 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 230000002747 voluntary effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 125000002256 xylenyl group Chemical class C1(C(C=CC=C1)C)(C)* 0.000 description 1
Landscapes
- Fixed Capacitors And Capacitor Manufacturing Machines (AREA)
- Encapsulation Of And Coatings For Semiconductor Or Solid State Devices (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明はセラミックコンデンサ、バリスター抵抗ネット
ワーク、ハイプリントICなどの電気・電子部品の粉体
塗装に於いて、密着性の良い下塗り塗料を適用して、耐
湿性、耐熱衝撃性を向上し、ピンホールなどの塗装欠陥
をも改良する電気絶縁方法に関するものである。[Detailed Description of the Invention] [Field of Industrial Application] The present invention applies an undercoat paint with good adhesion to powder coating of electrical and electronic components such as ceramic capacitors, varistor resistance networks, and high-print ICs. The present invention relates to an electrical insulation method that improves moisture resistance and thermal shock resistance, and also improves coating defects such as pinholes.
コンデンサ、バリスター、抵抗ネントワーク、ハイブリ
ッドICなどの電子部品を樹脂による絶縁外装する方法
には液状樹脂による注型、デイツプ、ドロップ、シーリ
ングや成形材料による封入成形や粉体塗装など各種ある
が、多様な形状の素子を比較的低コストで容易に外装す
ることができ、生産性の高い塗装法として粉体塗装が広
(採用されている。There are various methods for insulating and encasing electronic components such as capacitors, varistors, resistor networks, and hybrid ICs with resin, such as casting with liquid resin, dip, drop, sealing, encapsulation molding with molding materials, and powder coating. Powder coating is widely used as a highly productive coating method that allows devices of various shapes to be easily coated at relatively low cost.
粉体塗装方法としては、流動浸漬法、静1*動漫漬法、
ころがし法、ふりかけ法、静電スプレー法などがある。Powder coating methods include fluidized dipping method, static 1 * dynamic dipping method,
There are methods such as rolling method, sprinkle method, and electrostatic spray method.
これら粉体塗装製品に於いても、部品の信転性レベルは
益々高度化され、特に絶縁塗膜の耐ヒートサイクル性の
向上、耐湿性の向上が課題である。Even in these powder coated products, the reliability level of the parts is becoming increasingly sophisticated, and in particular, improvement of the heat cycle resistance and moisture resistance of the insulating coating film is a challenge.
耐ヒートサイクル性については、粉体塗料と基板の線膨
張係数が違うため、熱ストレスを加えると内部応力によ
るクランクが発生する。大型のハイブリッドICで著し
い場合は、導体パターンの剥離にもつながることがある
。Regarding heat cycle resistance, since the linear expansion coefficients of the powder coating and the substrate are different, if thermal stress is applied, internal stress will cause cranking. In severe cases in large hybrid ICs, this may lead to peeling of the conductor pattern.
二のようなことを解消するために粉体塗料の低応力化、
及び塗装方法の改善の両面から検討が行なわれている。In order to solve the second problem, reduce the stress of powder coating,
Studies are being carried out from the perspectives of both methods and improvement of coating methods.
粉体塗料に関しては耐ヒートサイクル性を向上させると
、耐湿性が悪化する傾向を示し、両立を計ることはむづ
かしいのが現状である。As for powder coatings, if heat cycle resistance is improved, moisture resistance tends to deteriorate, and it is currently difficult to achieve both.
また、塗装方法による粉体塗料のヒートサイクル性の向
上のために、シリコン樹脂やウレタン樹脂などのバッフ
ァー効果を有する下塗り材を適用する方法が採られてい
る。しかし、シリコン樹脂は密着性が悪く、透湿性があ
り、ウレタン樹脂は耐溶剤性、耐水性に欠点があり、い
ずれも耐ヒートサイクル性は向上するが、PCT等のき
びしい条件での耐湿性の向上は期待できず、かえって低
下してしまうものもある。Furthermore, in order to improve the heat cycle properties of powder coatings by coating methods, a method of applying an undercoat material having a buffer effect such as silicone resin or urethane resin has been adopted. However, silicone resin has poor adhesion and moisture permeability, while urethane resin has shortcomings in solvent resistance and water resistance.Although both improve heat cycle resistance, they have poor moisture resistance under severe conditions such as PCT. There are some things that cannot be expected to improve, and instead deteriorate.
下塗り材としては各種部品や外装材との密着性が良好で
、耐湿性、耐溶剤性、耐ヒートサイクル性に優れ、速硬
化で、−成型の材料であることが望ましい。As an undercoat material, it is desirable that the material has good adhesion to various parts and exterior materials, has excellent moisture resistance, solvent resistance, and heat cycle resistance, is fast curing, and can be molded.
本発明の目的とするところは、粉体塗装において密着性
と耐湿性のよい下塗り材を通用して、電気電子部品の耐
ヒートサイクル性の向上と耐湿性の向上の両立化が計れ
る粉体塗装法を提供するにある。An object of the present invention is to use a powder coating material that has good adhesion and moisture resistance to improve both heat cycle resistance and moisture resistance of electrical and electronic components. It is in providing the law.
本発明は、電気・電子部品を粉体塗料にて外装するに際
して、あらかじめフェノール樹脂とエポキシ化ポリブタ
ジェンを必須成分として含む下塗り材で塗装し、該塗料
を硬化後、粉体塗装してなる粉体塗装法である。When coating electrical and electronic components with a powder coating, the present invention applies an undercoating material containing phenol resin and epoxidized polybutadiene as essential components in advance, and after curing the coating material, the powder is coated with a powder coating. It is a painting method.
本発明に使用する下塗り材の一成分であるフェノール樹
脂にはレゾ−ル型フェノール樹脂とノボランク型フェノ
ール樹脂がある。レゾール型フェノール樹脂は、フェノ
ール類1モルに対し通常ホルムアルデヒドを1モル以上
、好ましくは1.1〜1.8モルで、かつ触媒として含
窒素化合物触媒、あるいは含窒素化合物とアルカリ土類
金属触媒を併用使用して、常法により縮合脱水させた樹
脂である。Phenolic resins that are one component of the undercoating material used in the present invention include resol type phenolic resins and novolanc type phenolic resins. The resol type phenolic resin usually contains 1 mol or more of formaldehyde, preferably 1.1 to 1.8 mol, per 1 mol of phenol, and also contains a nitrogen-containing compound catalyst, or a nitrogen-containing compound and an alkaline earth metal catalyst as a catalyst. These resins are used in combination and are condensed and dehydrated using conventional methods.
ここで言うフェノール類とは、フェノール、クレゾール
、キシレノール、レゾルシン、及びパラターシャリブチ
ルフェノール、バラオクチルフェノール、パラノニルフ
ェノール、バラフェニルフェノールなどのアルキルフェ
ノールである。The phenols mentioned here include phenol, cresol, xylenol, resorcinol, and alkylphenols such as paratertiary butylphenol, paraoctylphenol, paranonylphenol, and paraphenylphenol.
ホルムアルデヒドは通常ホルマリン水溶液の他にパラホ
ルムアルデヒドでもよい。Formaldehyde may be usually paraformaldehyde in addition to formalin aqueous solution.
含窒素化合物とは、アンモニア、トリエチルアミン、ト
リエタノールアミン、ジエチレンアミン、アニリン、ヘ
キサメチレンテトラミンなどである。Examples of nitrogen-containing compounds include ammonia, triethylamine, triethanolamine, diethyleneamine, aniline, hexamethylenetetramine, and the like.
アルカリ土類金属とは、カルシウム、マグネシウム、バ
リウムなどアルカリ土類金属の酸化物、水酸化物である
。Alkaline earth metals are oxides and hydroxides of alkaline earth metals such as calcium, magnesium, and barium.
レゾール型フェノール樹脂として、好ましくはアンモニ
ア、ヘキサメチレンテトラミンを反応触媒として使用し
たアンモニアレゾールである。好ましい触媒量はフェノ
ール100部に対して、NH。The resol type phenolic resin is preferably an ammonia resol using ammonia or hexamethylenetetramine as a reaction catalyst. A preferred amount of catalyst is NH per 100 parts of phenol.
とじて3〜15部である。The total amount is 3 to 15 parts.
ノボラック型フェノール樹脂は、前記レゾール型フェノ
ール樹脂中で記載したフェノール類とホルムアルデヒド
を用い、触媒としてシェラ酸などの有m酸及び塩酸、硫
酸などの無機酸を使用して、常法により縮合脱水させた
樹脂である。The novolak type phenolic resin is produced by condensation and dehydration using the phenols and formaldehyde described in the resol type phenol resin using a conventional method using an monic acid such as Scherer's acid and an inorganic acid such as hydrochloric acid or sulfuric acid as a catalyst. It is a resin.
さらに必要に応じて、これらのフェノール樹脂はキシレ
ン樹脂、メラミン樹脂、シリコン樹脂、植物油等で変性
したものであってもよい。Furthermore, if necessary, these phenolic resins may be modified with xylene resin, melamine resin, silicone resin, vegetable oil, or the like.
本発明に使用する下塗り材の他の成分であるエポキシ化
ポリブタジェンはポリブタジェンの主鎖中及び末端に複
数のエポキシ基を付与したもので、数平均分子量(Mn
)が600〜5000の液状ゴムである。例えば日本曹
達■製B F−1000、アデカアーガス化学■製B
F−1000、出光石油化学■製Po1y bd R4
5EPT、 Po1y bd R45EP+などを挙げ
ることができる。Epoxidized polybutadiene, which is another component of the undercoating material used in the present invention, is polybutadiene with a plurality of epoxy groups added in the main chain and at the ends, and has a number average molecular weight (Mn
) is 600 to 5000 liquid rubber. For example, Nippon Soda ■ B F-1000, Adeka Argus Chemical ■ B
F-1000, Poly bd R4 manufactured by Idemitsu Petrochemical ■
5EPT, Poly bd R45EP+, and the like.
これらのエポキシ化ポリブタジェンは塗料のタレを防止
する効果が期待できると共に塗膜に可撓性を付与して熱
衝撃性を向上し、硬化物の高周波特性向上を計ることが
できる。These epoxidized polybutadienes can be expected to have the effect of preventing paint from sagging, as well as impart flexibility to the coating film, improve thermal shock resistance, and improve the high frequency properties of the cured product.
これらエポキシ化ポリブタジェンの中でも、1、4結合
が50%以上のエポキシ化重合体が可撓性付与、他成分
との相溶性面より好ましい。Among these epoxidized polybutadienes, an epoxidized polymer having 50% or more of 1,4 bonds is preferable from the viewpoint of imparting flexibility and compatibility with other components.
また、ここでのエポキシ化ポリブタジェンの一部をたと
えば平均分子it 770以上のビスフェノールA型エ
ポキシ樹脂に部分置換して塗膜の諸持性を調整すること
もできる。Further, the durability of the coating film can be adjusted by partially substituting a part of the epoxidized polybutadiene with, for example, a bisphenol A type epoxy resin having an average molecular weight of 770 or more.
本発明に係る下塗り材成分の組成はフェノール樹脂とエ
ポキシ化ポリブタジェンの合計量に対して、フェノール
樹脂15〜85重量%、エポキシ化ポリブタジェン85
〜15重量%の範囲で使用できる。The composition of the undercoat component according to the present invention is 15 to 85% by weight of phenolic resin and 85% by weight of epoxidized polybutadiene, based on the total amount of phenolic resin and epoxidized polybutadiene.
It can be used in a range of 15% by weight.
更に、ポリビニルブチラール樹脂、フェノキシ樹脂、上
記以外のエボキン樹脂などの適宜配合することもできる
。Furthermore, polyvinyl butyral resin, phenoxy resin, Evoquine resin other than those mentioned above, etc. can also be appropriately blended.
本発明に使用する下塗り材に用いる溶剤は、トルエン、
キシレンなどの炭化水素系溶剤、エチルアルコールなど
のアルコール系溶剤、メチルエチルケントなどのゲント
系溶剤、セロソルブアセテート、醋酸ブチルなどのエス
テル系溶剤、メチルセロソルブ、エチルセロソルブなど
のセロソルブ系溶剤などの溶剤、1種または2種以上使
用する。The solvent used for the undercoat material used in the present invention is toluene,
Hydrocarbon solvents such as xylene, alcohol solvents such as ethyl alcohol, gent solvents such as methyl ethyl Kent, ester solvents such as cellosolve acetate and butyl acetate, cellosolve solvents such as methyl cellosolve and ethyl cellosolve, Use one or more types.
その他の添加剤については、密着性をより向上さるため
にシラン系カップリング剤やチタン系カップリングを含
有させることが好ましい。Regarding other additives, it is preferable to include a silane coupling agent or a titanium coupling agent in order to further improve adhesion.
また、必要に応じてイミダゾール類や芳香族アミン、有
機アルミニウム化合物などの硬化促進剤、消泡剤、タレ
止め剤、レベリング剤、染顔料など適量配合することが
できる。In addition, appropriate amounts of curing accelerators such as imidazoles, aromatic amines, and organoaluminum compounds, antifoaming agents, anti-sagging agents, leveling agents, dyes and pigments, etc. can be added as necessary.
この様にして得たー液型の下塗り材は、部品や基板及び
外装粉体塗料との密着性に優れ、特に、100μm以下
の薄膜で耐湿性、耐溶剤性、耐ヒートサイクル性に優れ
た効果を発揮することができる。The liquid-type undercoating material obtained in this way has excellent adhesion to parts, substrates, and exterior powder coatings, and in particular, has excellent moisture resistance, solvent resistance, and heat cycle resistance with a thin film of 100 μm or less. It can be effective.
(実施例) 以下、本発明を実施例により説明する。(Example) The present invention will be explained below using examples.
下塗り材に使用した樹脂組成及びその適用結果を表−1
に示す。Table 1 shows the resin composition used for the undercoat and its application results.
Shown below.
レゾール型フェノール樹脂は、フェノール類1モルに対
しホルムアデヒド1.2モルを配合し、表−1に示すそ
れぞれの触媒により常法により反応し、真空脱水後、メ
チルエチルケトン/メチルセロソルブ=1/2の混合溶
剤により溶解し、樹脂分50%に調整した。Resol type phenolic resin is made by mixing 1.2 moles of formadehyde with 1 mole of phenols, reacting with each catalyst shown in Table 1 in a conventional manner, and after vacuum dehydration, mixing methyl ethyl ketone/methyl cellosolve = 1/2. It was dissolved with a solvent and the resin content was adjusted to 50%.
ノボラック型フェノール樹脂はフェノール類1モルに対
しホルムアルデヒド0.9モル以下を配合し、表−1に
示す触媒により常法により反応し、真空脱水後メチルエ
チルケトン/メチルセロソルブ=1/2の混合溶剤によ
り溶解し、樹脂分50%に調整した。Novolak type phenolic resin is formulated with 0.9 mol or less of formaldehyde per 1 mol of phenols, reacted in a conventional manner with the catalyst shown in Table 1, and after vacuum dehydration, dissolved in a mixed solvent of methyl ethyl ketone/methyl cellosolve = 1/2. The resin content was adjusted to 50%.
ウレタン樹脂は2液硬化型で可撓性のあるもの(住友ベ
ークライト製r G CR−3200J )を、シリコ
ン樹脂は室温硬化型のもの(「信越シリコンKR−2S
IJ)をそれぞれ使用した。The urethane resin is a flexible two-component curing type (Sumitomo Bakelite rG CR-3200J), and the silicone resin is a room temperature curing type (Shin-Etsu Silicon KR-2S).
IJ) were used respectively.
特性測定試験に際して、素子としては横40m、縦20
m、厚み0.71のアルミナ仮にAg /Pdペースト
にて回路幅0.3mm、回路間0.31のくし型抵抗を
焼付け、リードフレームをとりつけたものを使用した。During the characteristic measurement test, the device was 40m wide and 20m long.
A comb-shaped resistor with a circuit width of 0.3 mm and a circuit spacing of 0.3 mm was baked with Ag/Pd paste, and a lead frame was attached to the alumina with a thickness of 0.71 m and a lead frame was used.
この素子に、表−1の各下塗り材をメチル七ロソで゛
ルブ冬希釈して粘度調整し、塗装膜厚20μmになるよ
うに塗布し、室温乾燥1時間後、110°C1時間、1
50°C1時間焼成硬化した。Each of the undercoating materials shown in Table 1 was diluted with methyl heptatoroso to adjust the viscosity and applied to this element to give a film thickness of 20 μm. After drying at room temperature for 1 hour, at 110°C for 1 hour,
It was baked and hardened at 50°C for 1 hour.
粉体塗装に当っては下記の通り実施した。Powder coating was carried out as follows.
(1)粉体塗料:エポキシ樹脂粉体塗料PR−5213
5(住友デュレズ■製)(2)塗装機 :流動浸漬塗装
機
■精研製PC−2S
(3)塗装条件:
下塗り材を塗装した素子をあらかじめ150’Cで30
分間予熱した後、粉体流動槽に3回浸漬し、粉体塗料を
付着させた後、150°C1時間硬化させて膜厚0.6
胴の評価用素子を作成した。(1) Powder coating: Epoxy resin powder coating PR-5213
5 (manufactured by Sumitomo Durez ■) (2) Painting machine: Fluid immersion coating machine ■ Seiken PC-2S (3) Painting conditions: The element coated with the undercoat material was preheated at 150'C for 30 minutes.
After preheating for 1 minute, immersion in a powder fluidization tank 3 times to adhere powder coating, and curing at 150°C for 1 hour to achieve a film thickness of 0.6
An element for evaluation of the torso was created.
なお、参考例は下塗り材を塗装せず、粉体塗料のみを塗
装した。In addition, in the reference example, no undercoat material was applied, and only powder paint was applied.
各特性の評価方法は次の通りである。The evaluation method for each characteristic is as follows.
下塗り材の耐溶剤性:下塗り材を塗布した素子をメチル
エチルケント液中に1時間浸漬し、下塗り材の塗膜の膨
潤を無を観察した。Solvent resistance of undercoat material: The element coated with the undercoat material was immersed in a methyl ethyl Kent solution for 1 hour, and the swelling of the coating film of the undercoat material was observed.
膨潤しないものをO1膨潤したものを×と表示した。Those that did not swell and those that swelled with O1 were indicated as ×.
耐湿性:評価用素子をプレッシャークツカー試験機にて
121°C1150時間吸湿処理後、回路間の絶縁抵抗
変化により耐湿性を評価した。(初期値10′)Ω)
耐ヒートサイクル性二評価用素子を125°C30分間
と一40°C30分間の熱衝撃を与え、50%の試料に
塗膜のクラックが発生するまでのサイクル数(回)を求
めた。Moisture resistance: After the evaluation element was subjected to moisture absorption treatment at 121° C. for 1150 hours using a pressure cutter tester, moisture resistance was evaluated based on changes in insulation resistance between circuits. (Initial value 10') Ω) The heat cycle resistance second evaluation element was subjected to thermal shock at 125°C for 30 minutes and at 140°C for 30 minutes, and the number of cycles until cracks occurred in the coating film in 50% of the samples ( times) was calculated.
本発明の方法に従うと、従来のシリコン樹脂、ウレタン
樹脂による下塗り塗装方法の欠点を克服し、耐ヒートサ
イクル性はもとより、耐湿性を向上することができる。According to the method of the present invention, the drawbacks of conventional undercoating methods using silicone resins and urethane resins can be overcome, and not only heat cycle resistance but also moisture resistance can be improved.
特にバリスター、ハイプリントICに適用した場合、信
績度の高い塗装品が得られる。また、モールド部品搭載
品に通用した場合、個別部品と基板との空隙部の空気だ
まりに起因するフクレ、ピンホールなどの塗膜欠陥をも
本塗装方法は改善できる。Particularly when applied to varistors and high print ICs, coated products with high reliability can be obtained. Furthermore, when applied to products with molded components, this coating method can also improve coating film defects such as blisters and pinholes caused by air pockets in the gaps between individual components and the board.
手続補正書(自発) 平成1年11月Procedural amendment (voluntary) November 1999
Claims (1)
て、部品をあらかじめフェノール樹脂とエポキシ化ポリ
ブタジエンを必須成分として含む下塗り材で塗装し、該
塗料を硬化後、粉体塗装してなる粉体塗装法。(1) When coating electrical/electronic parts with powder coating, the parts are first coated with an undercoat containing phenolic resin and epoxidized polybutadiene as essential components, and after the coating has hardened, powder coating is applied. Body painting method.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1144002A JPH0312260A (en) | 1989-06-08 | 1989-06-08 | Powder painting method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1144002A JPH0312260A (en) | 1989-06-08 | 1989-06-08 | Powder painting method |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0312260A true JPH0312260A (en) | 1991-01-21 |
Family
ID=15352034
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1144002A Pending JPH0312260A (en) | 1989-06-08 | 1989-06-08 | Powder painting method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0312260A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH08339942A (en) * | 1995-06-09 | 1996-12-24 | Nec Kansai Ltd | Electronic component |
-
1989
- 1989-06-08 JP JP1144002A patent/JPH0312260A/en active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH08339942A (en) * | 1995-06-09 | 1996-12-24 | Nec Kansai Ltd | Electronic component |
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