JPS62195200A - Ag/ni covered cu powder - Google Patents
Ag/ni covered cu powderInfo
- Publication number
- JPS62195200A JPS62195200A JP3524986A JP3524986A JPS62195200A JP S62195200 A JPS62195200 A JP S62195200A JP 3524986 A JP3524986 A JP 3524986A JP 3524986 A JP3524986 A JP 3524986A JP S62195200 A JPS62195200 A JP S62195200A
- Authority
- JP
- Japan
- Prior art keywords
- powder
- conductive
- conductivity
- coated
- oxidation resistance
- 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.)
- Granted
Links
- 239000000843 powder Substances 0.000 title claims description 24
- 229910052709 silver Inorganic materials 0.000 claims description 8
- 239000011247 coating layer Substances 0.000 claims description 7
- 229910052759 nickel Inorganic materials 0.000 claims description 6
- 239000002245 particle Substances 0.000 claims description 6
- 229910052763 palladium Inorganic materials 0.000 claims 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 18
- 239000011347 resin Substances 0.000 description 11
- 229920005989 resin Polymers 0.000 description 11
- 239000003973 paint Substances 0.000 description 9
- 230000003647 oxidation Effects 0.000 description 8
- 238000007254 oxidation reaction Methods 0.000 description 8
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 6
- 238000000576 coating method Methods 0.000 description 6
- 239000007864 aqueous solution Substances 0.000 description 5
- KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 5
- 238000000034 method Methods 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 238000007747 plating Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 239000011231 conductive filler Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000006258 conductive agent Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 230000007257 malfunction Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- LGQLOGILCSXPEA-UHFFFAOYSA-L nickel sulfate Chemical compound [Ni+2].[O-]S([O-])(=O)=O LGQLOGILCSXPEA-UHFFFAOYSA-L 0.000 description 1
- 229910000363 nickel(II) sulfate Inorganic materials 0.000 description 1
- PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- HAAYBYDROVFKPU-UHFFFAOYSA-N silver;azane;nitrate Chemical compound N.N.[Ag+].[O-][N+]([O-])=O HAAYBYDROVFKPU-UHFFFAOYSA-N 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
- Paints Or Removers (AREA)
- Chemically Coating (AREA)
- Shielding Devices Or Components To Electric Or Magnetic Fields (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
く技術分野〉
近年、コンピューター機器が広汎に用いられているが、
外部の電磁波が該コンピューター機器に影響し、誤作動
の原因となることが指摘されている。これはコンピュー
ターの筐体部呻有機樹脂が使用され、有機樹脂では電波
が通過するためである。こり防止対策として有機樹脂を
導電性化して電磁シールドの効果を発揮させることが行
われている。[Detailed Description of the Invention] Technical Field> In recent years, computer equipment has been widely used, but
It has been pointed out that external electromagnetic waves affect computer equipment and cause malfunctions. This is because organic resin is used for computer housings, and radio waves can pass through organic resin. As a measure to prevent stiffness, organic resins are made conductive to provide an electromagnetic shielding effect.
本発明は、特に有機樹脂に混じて該樹脂を導電性化する
に適するNiとAgで被覆したCu粉末に関する。The present invention relates to Cu powder coated with Ni and Ag, which is particularly suitable for mixing with organic resins to make the resins conductive.
〈従来技術とその問題点〉 有機樹脂を導電性化する方法としては ■有機樹脂に導電フィラーを含有させる。<Conventional technology and its problems> How to make organic resin conductive ■Incorporating a conductive filler into the organic resin.
■有機樹脂材の表面を金属亜鉛の溶射等によりメタライ
ズする。■Metallize the surface of the organic resin material by spraying metal zinc.
■有機樹脂材表面に導電塗料を塗布する。■Apply conductive paint to the surface of organic resin material.
等の方法が知られているが、最も広く行われてぃる方法
は■である。The following methods are known, but the most widely used method is (2).
導電塗料は塗料中に導電粉末を含有させたものであるが
、磁気シールドの目的には帯電防止用などよりは高度に
導電性にしなければならないので、充填用の導電粉末と
しては、Nj、 CLI、 Ag等が使用されている。Conductive paint is made by containing conductive powder in the paint, but for the purpose of magnetic shielding, it must be highly conductive rather than for antistatic purposes, so Nj, CLI, etc. are used as conductive powder for filling. , Ag, etc. are used.
この中でAgは最も導電性が高く、耐酸化性があり、長
時間放置しても劣化がないが高価である。またCuは安
価であり導電性も優れているが、酸化され易く、長期に
わたる耐久性に欠ける。Niは耐久性はあるが、Cu及
びAgよりも導電性が劣る。Among these, Ag has the highest conductivity and oxidation resistance, and does not deteriorate even if left for a long time, but it is expensive. Further, although Cu is inexpensive and has excellent conductivity, it is easily oxidized and lacks long-term durability. Although Ni is durable, it has poorer conductivity than Cu and Ag.
本発明は導電塗料に用いる導電粉末に関するものでCu
の耐酸化性と導電性を向上させることにその目的がある
。The present invention relates to conductive powder used in conductive paint, and relates to conductive powder used in conductive paint.
Its purpose is to improve the oxidation resistance and conductivity of
Cuの耐酸化性を向上させる目的で塗料中に酸化防止剤
を含有させることが試みられているが、有機物質が主で
あり、満足すべきものはない。又CuにAgを被覆する
ことも知られているが、耐酸化性を生じさせるほどAg
を被覆するとAgの被覆量が多くなり高価なものとなる
。Attempts have been made to include antioxidants in paints for the purpose of improving the oxidation resistance of Cu, but organic substances are the main ingredient, and nothing is satisfactory. It is also known to coat Cu with Ag.
If it is coated with Ag, the amount of Ag coated will be large and the product will be expensive.
本発明者らはCu粉末の表面にNiを被覆することで耐
酸化性を高めることを検討した。しかしNiを被覆する
と耐酸化性はNjと同等となるが導電性はCuよりも低
下した。The present inventors investigated increasing the oxidation resistance by coating the surface of Cu powder with Ni. However, when coated with Ni, the oxidation resistance was equal to that of Nj, but the conductivity was lower than that of Cu.
このため本発明者らはこのNi被覆Cu粉末の上に更に
Agを少量被覆することで導電性をAB、 Cuと同等
に高めることが可能となった。即ち、耐酸化性をNiで
出現させ導電性をAg、 Cuで出現させた画期的な粉
末を見出した。Therefore, the present inventors were able to further increase the conductivity to the same level as AB and Cu by further coating a small amount of Ag on top of the Ni-coated Cu powder. That is, we have discovered an innovative powder that exhibits oxidation resistance with Ni and conductivity with Ag and Cu.
〈発明の構成〉
本発明によれば、Cu粒子の核と
Cu重量に対して
0.01〜0.2%のPdの第1被覆層]、 〜10.
0%のNiの第2被覆層0.2〜5.0%のAgの第3
被覆層
からなるAg、 Ni被覆Cu粉末が提供される。<Configuration of the Invention> According to the present invention, the core of the Cu particles and the first coating layer of Pd in an amount of 0.01 to 0.2% based on the weight of Cu], ~10.
A second coating layer of 0% Ni, a third coating layer of 0.2-5.0% Ag.
A Ag, Ni-coated Cu powder comprising a coating layer is provided.
本発明のAg、 Ni被覆粒子において使用されるCu
粉末の粒度は特に限定されないが、好ましくは0.5〜
500μ、より好ましくは1〜100μである。Cu used in Ag, Ni-coated particles of the present invention
The particle size of the powder is not particularly limited, but is preferably from 0.5 to
It is 500μ, more preferably 1 to 100μ.
純度も特に限定されない。Purity is also not particularly limited.
Pdの第1層はNiめっきのため下地として必然的に形
成されるもので、本発明において積極的意味を有しない
。The first layer of Pd is necessarily formed as a base for Ni plating, and has no positive meaning in the present invention.
Cu粉末にNiを被覆する方法は通常の化学メッキ法で
行える。即ち、Cu粉末にPdを被着した後、Ni水溶
液に懸濁させ、これにヒドラジン等の還元剤を加えるこ
とでNiがCu粉の表面に析出する。さらにAgを被覆
することも化学メッキで行える。即ち、Ni被覆Cu粉
末をアンモニア性Ag水溶液中に懸濁させ、ホルマリン
、酒石酸等の還元剤を加えることで目的の粉末が得られ
る。The method of coating the Cu powder with Ni can be performed by a normal chemical plating method. That is, after depositing Pd on Cu powder, it is suspended in a Ni aqueous solution and a reducing agent such as hydrazine is added thereto, thereby causing Ni to precipitate on the surface of the Cu powder. Furthermore, coating with Ag can also be performed by chemical plating. That is, the desired powder can be obtained by suspending Ni-coated Cu powder in an ammoniacal Ag aqueous solution and adding a reducing agent such as formalin or tartaric acid.
Niの被覆量としてはCu重量に対して0.5〜10ν
t%である。0.5wt%未満であるとNiの被覆が完
全でなく耐酸化性を保持出来ない。また10wt%を越
えると導電性が低下しAgの被覆量が多く必要とする。The amount of Ni covered is 0.5 to 10ν relative to the weight of Cu.
t%. If it is less than 0.5 wt%, the Ni coating will not be complete and oxidation resistance cannot be maintained. Moreover, if it exceeds 10 wt%, the conductivity decreases and a large amount of Ag is required to be coated.
Agの被覆は0.2〜5.0w七%が適当である。0.
2wt%未満であると導電性が出す、5 、0wt%を
越えても導電性の効果はほとんど変らない。A suitable Ag coating is 0.2 to 5.0w 7%. 0.
If it is less than 2 wt%, the conductivity will be improved, and if it exceeds 5.0 wt%, the conductivity effect will hardly change.
本発明による粉末は電磁シールドに用いる導電塗料の導
電フィラーのみならず、導電ペースト用のフィラーとし
ても併用出来ることは言うまでもない。It goes without saying that the powder according to the present invention can be used not only as a conductive filler for conductive paints used for electromagnetic shielding, but also as a filler for conductive pastes.
〈発明の具体的記載〉
実施例
Cu粉末(幅用金属ハク社製、粒度3oμm) 10g
を塩化パラジウム水溶液(Pdとして0.3gIQ濃度
)中に浸漬し、表面にPdを被着させた後、硫酸ニッケ
ル水溶液中に懸濁し、60℃に保ちながらヒドラジン(
0,5〜4g)を加え、約1時間反応させてNiを粒子
表面に析出させた。Niの析出量は0.5〜l Qwt
%まで変化させた。次に、この粉末を集めてアンモニア
性硝酸銀水溶液中に懸濁し、これにヒドラジンを加えA
gを析出させた粉末を集め水洗乾燥した。<Specific description of the invention> Example Cu powder (manufactured by Width Metal Haku Co., Ltd., particle size 3oμm) 10g
was immersed in a palladium chloride aqueous solution (0.3 g IQ concentration as Pd) to deposit Pd on the surface, then suspended in a nickel sulfate aqueous solution, and hydrazine (
0.5 to 4 g) was added and reacted for about 1 hour to precipitate Ni on the particle surface. The amount of Ni precipitation is 0.5~l Qwt
It was changed up to %. Next, this powder was collected and suspended in an ammoniacal silver nitrate aqueous solution, and hydrazine was added to it.
The powder from which g was precipitated was collected, washed with water, and dried.
Agの析出量は0.2〜5.0wt%まで変化させた。The amount of Ag precipitated was varied from 0.2 to 5.0 wt%.
この粉末をアクリル塗料(関西ペイント(株)アクリツ
ク200樹脂35wt%、アセトン、MEK、トルエン
混合溶剤65wt%)に加え、ホモミキサーを用い、2
000r、pomで15分間分散し、導電性アクリル塗
料を作製、これをアクリル板の上に50μmの厚さで塗
布し、電気伝導度、耐酸化性等の試験を行った。This powder was added to acrylic paint (Kansai Paint Co., Ltd. Acryk 200 resin 35 wt%, acetone, MEK, toluene mixed solvent 65 wt%), and using a homo mixer, 2
A conductive acrylic paint was prepared by dispersing it at 000r and pom for 15 minutes, and this was applied onto an acrylic plate to a thickness of 50 μm, and tests for electrical conductivity, oxidation resistance, etc. were conducted.
結果を表に示す。The results are shown in the table.
表
0.5 0 1.I
XO,541,1Δ
1.0 3 1.1
02.0 0 3.0
02.00゜2 1.8
02.0 0.5 1.
2 02.0 1.0
1.1 02.0 5.
0 1.0 05.0
0 6 05.0
0.2 2.0 0
10.0 0 8
010.0 1.0 1.6
0この結果は本発明の粉末が有機樹脂
に混する導電性化剤としてCu粉末に比して極めて優れ
ていることを物語っている。Table 0.5 0 1. I
XO,541,1Δ 1.0 3 1.1
02.0 0 3.0
02.00゜2 1.8
02.0 0.5 1.
2 02.0 1.0
1.1 02.0 5.
0 1.0 05.0
0 6 05.0
0.2 2.0 0
10.0 0 8
010.0 1.0 1.6
0 This result proves that the powder of the present invention is extremely superior to Cu powder as a conductive agent to be mixed into an organic resin.
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61035249A JPH0797717B2 (en) | 1986-02-21 | 1986-02-21 | Cu powder coated with Ag and Ni |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61035249A JPH0797717B2 (en) | 1986-02-21 | 1986-02-21 | Cu powder coated with Ag and Ni |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62195200A true JPS62195200A (en) | 1987-08-27 |
JPH0797717B2 JPH0797717B2 (en) | 1995-10-18 |
Family
ID=12436555
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61035249A Expired - Lifetime JPH0797717B2 (en) | 1986-02-21 | 1986-02-21 | Cu powder coated with Ag and Ni |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0797717B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002075057A (en) * | 2000-08-30 | 2002-03-15 | Mitsui Mining & Smelting Co Ltd | Coated copper powder |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60162779A (en) * | 1984-02-06 | 1985-08-24 | Nippon Chem Ind Co Ltd:The | Silver plated composition and its manufacture |
JPS60177183A (en) * | 1984-02-24 | 1985-09-11 | Nippon Chem Ind Co Ltd:The | Silver plated composition and its manufacture |
-
1986
- 1986-02-21 JP JP61035249A patent/JPH0797717B2/en not_active Expired - Lifetime
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60162779A (en) * | 1984-02-06 | 1985-08-24 | Nippon Chem Ind Co Ltd:The | Silver plated composition and its manufacture |
JPS60177183A (en) * | 1984-02-24 | 1985-09-11 | Nippon Chem Ind Co Ltd:The | Silver plated composition and its manufacture |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002075057A (en) * | 2000-08-30 | 2002-03-15 | Mitsui Mining & Smelting Co Ltd | Coated copper powder |
Also Published As
Publication number | Publication date |
---|---|
JPH0797717B2 (en) | 1995-10-18 |
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