JPH01247501A - Electrically conductive particles - Google Patents
Electrically conductive particlesInfo
- Publication number
- JPH01247501A JPH01247501A JP7787188A JP7787188A JPH01247501A JP H01247501 A JPH01247501 A JP H01247501A JP 7787188 A JP7787188 A JP 7787188A JP 7787188 A JP7787188 A JP 7787188A JP H01247501 A JPH01247501 A JP H01247501A
- Authority
- JP
- Japan
- Prior art keywords
- parts
- resin powder
- conductive particles
- electrically conductive
- axis size
- 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
- 239000002245 particle Substances 0.000 title claims abstract description 32
- 239000000843 powder Substances 0.000 claims abstract description 19
- 239000011347 resin Substances 0.000 claims abstract description 15
- 229920005989 resin Polymers 0.000 claims abstract description 15
- 229910052751 metal Inorganic materials 0.000 claims abstract description 11
- 239000002184 metal Substances 0.000 claims abstract description 11
- 238000007747 plating Methods 0.000 claims abstract description 10
- 239000003973 paint Substances 0.000 abstract description 11
- 239000006185 dispersion Substances 0.000 abstract description 7
- 229910052802 copper Inorganic materials 0.000 abstract description 5
- 229910052759 nickel Inorganic materials 0.000 abstract description 4
- 229910052709 silver Inorganic materials 0.000 abstract description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- 238000003756 stirring Methods 0.000 description 12
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 6
- -1 polyoxyethylene nonylphenyl ether Polymers 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
- 239000004698 Polyethylene Substances 0.000 description 4
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 4
- 239000010949 copper Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229920000573 polyethylene Polymers 0.000 description 4
- KMUONIBRACKNSN-UHFFFAOYSA-N potassium dichromate Chemical compound [K+].[K+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O KMUONIBRACKNSN-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 239000008096 xylene Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 239000004677 Nylon Substances 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 229920001778 nylon Polymers 0.000 description 3
- 239000004332 silver Substances 0.000 description 3
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000011259 mixed solution Substances 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 238000004062 sedimentation Methods 0.000 description 2
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 2
- KWSLGOVYXMQPPX-UHFFFAOYSA-N 5-[3-(trifluoromethyl)phenyl]-2h-tetrazole Chemical compound FC(F)(F)C1=CC=CC(C2=NNN=N2)=C1 KWSLGOVYXMQPPX-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- KXZJHVJKXJLBKO-UHFFFAOYSA-N chembl1408157 Chemical compound N=1C2=CC=CC=C2C(C(=O)O)=CC=1C1=CC=C(O)C=C1 KXZJHVJKXJLBKO-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000004570 mortar (masonry) Substances 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
- 229910052763 palladium Inorganic materials 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- LFAGQMCIGQNPJG-UHFFFAOYSA-N silver cyanide Chemical compound [Ag+].N#[C-] LFAGQMCIGQNPJG-UHFFFAOYSA-N 0.000 description 1
- 229940098221 silver cyanide Drugs 0.000 description 1
- 229910001961 silver nitrate Inorganic materials 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- HELHAJAZNSDZJO-OLXYHTOASA-L sodium L-tartrate Chemical compound [Na+].[Na+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O HELHAJAZNSDZJO-OLXYHTOASA-L 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 229910001379 sodium hypophosphite Inorganic materials 0.000 description 1
- 239000001433 sodium tartrate Substances 0.000 description 1
- 229960002167 sodium tartrate Drugs 0.000 description 1
- 235000011004 sodium tartrates Nutrition 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Paints Or Removers (AREA)
- Powder Metallurgy (AREA)
- Electroplating Methods And Accessories (AREA)
- Conductive Materials (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野コ
本発明は、電気回路用、電磁波シールド用などの導電性
塗料に用いられる導電性粒子に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to conductive particles used in conductive paints for electrical circuits, electromagnetic shielding, and the like.
[従来の技術及びその課題]
従来使用されている導電性粒子としては各種金属粉、導
電性カーボンなどがあるが、これらの導電性粒子は、そ
の比重が大きいことから、導電性塗料に用いた場合分散
安定性が悪く、沈降が早いという欠点があり、又、有機
及び/又は無機の粉体に銀や銅、ニッケル等の金属をメ
ッキした導電性粒子も知られているが、無機粉体は、均
一なメッキ層の形成が困難であり、高導電性が得られ難
く、又、有機粉体は、その形状が球又は不定形であるた
め、塗料としたとき粒子同志の接触面積が小さいため導
電性が劣るという欠点があった。[Prior art and its problems] Conventionally used conductive particles include various metal powders and conductive carbon, but these conductive particles have a high specific gravity, so they have not been used in conductive paints. However, conductive particles made by plating organic and/or inorganic powder with metals such as silver, copper, and nickel are also known; It is difficult to form a uniform plating layer and it is difficult to obtain high conductivity, and organic powder has a spherical or irregular shape, so when used as a paint, the contact area between particles is small. Therefore, it had the disadvantage of poor conductivity.
本発明は、上記せる分散安定性、導電性の開運を解決し
た導電性粒子を提供することを目的とするものである。The object of the present invention is to provide conductive particles that solve the above problems of dispersion stability and conductivity.
[課題を解決するための手段]
本発明は、平均粒子径が100μm以下、短径が長径の
171〜1/10.厚みが長径の1/2〜1150の範
囲にある扁平状微小樹脂粉に金属をメッキすることによ
り前記せる欠点のない導電性粒子を提供できることを見
出すことによって達成されたものである。[Means for Solving the Problems] The present invention provides particles having an average particle size of 100 μm or less, and a short axis of 171 to 1/10 of the long axis. This was achieved by discovering that it is possible to provide conductive particles without the above-mentioned drawbacks by plating flat microscopic resin powder with a thickness in the range of 1/2 to 1150 mm of the major axis with metal.
以下、本発明の詳細な説明する。The present invention will be explained in detail below.
本発明において、核となる扁平状微小樹脂粉は、本願出
願人が先に提案した特願昭60−244297号に記載
した方法により得られるものや、市販のものが使用でき
る。又、上記扁平状微小樹脂粉を金属メッキするには、
従来公知の方法を用いることができ、用いる金属として
は、特に限定はないが。In the present invention, the flat microscopic resin powder serving as the core can be obtained by the method described in Japanese Patent Application No. 60-244297, which was previously proposed by the applicant of the present application, or a commercially available powder. In addition, in order to metal plate the flat micro resin powder,
Conventionally known methods can be used, and the metal used is not particularly limited.
銀、銅、ニッケル等が、高い導電性を得る上で好ましい
。Silver, copper, nickel, etc. are preferable in order to obtain high conductivity.
[作 用]
本発明に係る導電性粒子は、軽い樹脂粉のまわりを金属
メッキ層で覆っているため全体としての比重が小さくな
り、分散安定性が向上し、更には、核となる樹脂粉に扁
平なものを用いているため、該粒子の接触が面で行なわ
れ、従来の球又は不定形のものの点接触よりも接触面積
が大きく、高い導電性が得られると考えられる。[Function] Since the conductive particles according to the present invention cover the light resin powder with a metal plating layer, the overall specific gravity is reduced, the dispersion stability is improved, and furthermore, the core resin powder is Since the particles are flat, the particles come into contact with each other on the surface, and the contact area is larger than that of conventional point contact made of spheres or irregularly shaped particles, and it is thought that high conductivity can be obtained.
[実施例] 以下実施例にて本発明を更に詳細に説明するが。[Example] The present invention will be explained in more detail with reference to Examples below.
実施例中1部」とあるのは「重量部」を示す。In the examples, "1 part" indicates "part by weight."
失五災よ
球状ナイロン(@東し1 10部平均粒子
径5μm)
ニラコールNP−10(日光ケミ 0.1部カルズ
社製、ポリオキシエチレ
ンノニルフェニルエーテル)
水
60部上記成分を混合撹拌した後、磁性ボール200
gを入れた容量300m1の磁性ポットに入れ、36時
間混合した後、濾過、乾燥して、平均長径16μm、平
均短径13μm、平均厚さ1.6μm、の扁平状微小樹
脂粉を得た0次に、重クロム酸カリウム12.5部を水
100部に加熱溶解し、更に濃硫酸50部を撹拌しなが
ら加えた液に、上記扁平状微小樹脂粉を加え70℃にて
15分間撹拌した後、濾過・水洗し、これを5%塩酸水
溶液に投入、1部分間撹拌して濾過した。更にこのもの
をキャタリストC(触媒金属パラジウム付与剤、奥野製
薬工業■製)40部、製塩8140部の混合液中に投入
し10分間撹拌した後濾過・水洗し、次いで硫酸網29
部、炭酸ナトリウム25部、水酸化ナトリウム40部、
ロッセル塩140部を水1000部に溶解した液に投入
し、撹拌しながら35%ホルムアルデヒド水溶液150
部を徐々に投入して、液の色が略なくなるまで反応を行
なった後、濾過・水洗・乾燥して銅メッキした扁平状微
小ナイロンを得た。Spherical nylon (@Higashishi 1, 10 parts, average particle diameter 5 μm), Nylacol NP-10 (Nikko Chemi, 0.1 part, manufactured by Cals Co., Ltd., polyoxyethylene nonylphenyl ether), water
After mixing and stirring 60 parts of the above ingredients, 200 parts of magnetic balls were added.
After mixing for 36 hours, it was filtered and dried to obtain flat micro resin powder with an average major axis of 16 μm, an average minor axis of 13 μm, and an average thickness of 1.6 μm. Next, 12.5 parts of potassium dichromate was heated and dissolved in 100 parts of water, and 50 parts of concentrated sulfuric acid was added with stirring. The above flat resin powder was added to the solution and stirred at 70°C for 15 minutes. After that, the mixture was filtered and washed with water, poured into a 5% aqueous hydrochloric acid solution, stirred for 1 portion, and filtered. Further, this product was added to a mixed solution of 40 parts of Catalyst C (catalytic metal palladium imparting agent, manufactured by Okuno Pharmaceutical Co., Ltd.) and 8140 parts of salt preparation, stirred for 10 minutes, filtered and washed with water, and then sulfuric acid net 29
parts, 25 parts of sodium carbonate, 40 parts of sodium hydroxide,
Add 140 parts of Rossell's salt to 1000 parts of water and add 150 parts of 35% formaldehyde aqueous solution while stirring.
After the reaction was carried out until the color of the liquid almost disappeared, the mixture was filtered, washed with water, and dried to obtain copper-plated flat microscopic nylon.
大嵐叢主
球状ポリスチレン(住人化学工業 10部tmia
、平均粒子径15μm)
ニア:I−ルDLP−10(日光ケ 0.2部ミカル
ズ社製、ポリオキシエチ
レンラウリルエーテルリン酸
ナトリウム)
水
40部上記成分を混合撹拌した後、自動乳鉢にて5時間
混合を行ない、濾過、乾燥して、扁平状微小樹脂粉を得
た。このものは平均長径24μm、平均短径18μm、
平均厚み7μmであった。このものを実施例1と同様に
なして銅メッキを施した後。Daiarashiso main spherical polystyrene (Jumin Chemical Industry 10 parts tmia
, average particle size 15 μm) Near: I-L DLP-10 (Nikko Kei 0.2 parts manufactured by Michals, sodium polyoxyethylene lauryl ether phosphate) Water
After mixing and stirring 40 parts of the above components, the mixture was mixed in an automatic mortar for 5 hours, filtered and dried to obtain flat microscopic resin powder. This item has an average major axis of 24 μm, an average minor axis of 18 μm,
The average thickness was 7 μm. After copper plating was applied to this product in the same manner as in Example 1.
シアン化銀7.5部とシアン化ナトリウム15部とを水
1000部に溶かした液に撹拌しながら投入して20分
間撹拌した後、濾過・水洗・乾燥して銀メッキした扁平
状微小ポリスチレンを得た。Add 7.5 parts of silver cyanide and 15 parts of sodium cyanide to a solution of 1000 parts of water with stirring, stir for 20 minutes, filter, wash, and dry to obtain silver-plated flat polystyrene. Obtained.
失胤気ユ
破砕状ポリエチレン(製鉄化学@ 10部製、平均
粒子径20μm)
ベンゼン 35部上記成分を
、磁性ボール200gを入れた容量300+++1の磁
性ポットに入れ、4時間混合させた後、濾過・乾燥して
、扁平状微小樹脂粉を得た。Crushed polyethylene (manufactured by Seitetsu Kagaku @ 10 parts, average particle size 20 μm) 35 parts of benzene The above ingredients were placed in a magnetic pot with a capacity of 300++1 containing 200 g of magnetic balls, mixed for 4 hours, and then filtered. It was dried to obtain flat microscopic resin powder.
このものは平均長径48μm、平均短径37μm、平均
厚さ24μm、であった。次に、重クロム酸カリウム1
2.5部を水100部に加熱溶解し、更に濃硫酸50部
を撹拌しながら加えた液に、上記扁平状微小樹脂粉を加
え70℃にて15分間撹拌した後、濾過・水洗し、これ
を5%塩酸水溶液に投入、1部分間撹拌して濾過した。This material had an average major axis of 48 μm, an average minor axis of 37 μm, and an average thickness of 24 μm. Next, potassium dichromate 1
2.5 parts were heated and dissolved in 100 parts of water, and 50 parts of concentrated sulfuric acid was added with stirring.The above flat resin powder was added to the solution, stirred at 70°C for 15 minutes, filtered and washed with water, This was poured into a 5% aqueous hydrochloric acid solution, stirred for 1 portion, and filtered.
更にこのものをキャタリストC40部、濃塩酸140部
の混合液中に投入し10分間撹拌した後濾過・水洗し。Further, this product was added to a mixed solution of 40 parts of Catalyst C and 140 parts of concentrated hydrochloric acid, stirred for 10 minutes, and then filtered and washed with water.
次いで硫酸ニッケル30部、酒石酸ナトリウム30部、
プロピオン酸4部を水1000部に溶解した液に投入し
、撹拌しながら55℃に加熱した後、次亜リン酸ナトリ
ウム15部を徐々に加え、30分間撹拌して濾過・水洗
・乾燥してニッケルメッキした扁平状微小ポリエチレン
を得た。Next, 30 parts of nickel sulfate, 30 parts of sodium tartrate,
Add 4 parts of propionic acid to 1000 parts of water and heat to 55°C with stirring, then gradually add 15 parts of sodium hypophosphite, stir for 30 minutes, filter, wash with water, and dry. A flat microscopic polyethylene plated with nickel was obtained.
これを更に、硝酸銀15部、アンモニア水150部を水
1ooO部に溶解した液中に投入し、撹拌しなからチオ
硫酸ナトリウム210部を徐々に添加して30分間撹拌
した後、濾過・水洗・乾燥して銀メッキした扁平状微小
ポリエチレンを得た。This was further poured into a solution in which 15 parts of silver nitrate and 150 parts of aqueous ammonia were dissolved in 100 parts of water, and 210 parts of sodium thiosulfate was gradually added without stirring. After stirring for 30 minutes, filtration, washing with water, After drying, silver-plated flat microscopic polyethylene was obtained.
以上実施例1〜3で得られた導電性粒子の表面を電子顕
微鏡でa察したところいずれも核となる扁平状微小樹脂
粉のまわりを金属メッキ層が覆っていることが確認され
た。When the surfaces of the conductive particles obtained in Examples 1 to 3 were observed using an electron microscope, it was confirmed that in each case, a metal plating layer covered the flat microscopic resin powder serving as the core.
応用例1
実施例1で得られた導電性粒子 60部バリアク
ロン8001 (播磨化成 20部工業■製、接着
剤)
キシレン 2o部上記成分
を混合、撹拌して導電性塗料を得た。Application Example 1 60 parts of conductive particles obtained in Example 1 Barracron 8001 (20 parts manufactured by Harima Kasei, adhesive) 20 parts of xylene The above components were mixed and stirred to obtain a conductive paint.
妄皿璽ス
実施例2で得られた導電性粒子 60部バリアク
ロン8001 20部キシレン
20部上記成分を混合、撹拌して
導電性塗料を得た。Conductive particles obtained in Example 2 60 parts Barracron 8001 20 parts xylene
20 parts of the above components were mixed and stirred to obtain a conductive paint.
応JD」l
実施例3で得られた導電性粒子 60部バリアク
ロン8001 20部キシレン
20部上記成分を混合、撹拌して
導電性塗料を得た。Conductive particles obtained in Example 3 60 parts Barracron 8001 20 parts xylene
20 parts of the above components were mixed and stirred to obtain a conductive paint.
ル較五上
市販銀粉(平均粒子径10μm 60部鱗片状
)
バリアクロン8001 20部キシレン
20部上記成分を混合、
撹拌して導電性塗料を得た。Commercially available silver powder (average particle size 10 μm, 60 parts scaly) Barracron 8001 20 parts xylene 20 parts Mix the above ingredients,
A conductive paint was obtained by stirring.
よ較■裟
実施例1で用いた球状ナイロンを扁平化せずにそのまま
用い、実施例1と同様に銅メッキを施し、導電性粒子を
得た後、応用例3と同様にして導電性塗料を得た。For comparison, the spherical nylon used in Example 1 was used as it was without being flattened, and after copper plating was applied in the same manner as in Example 1 to obtain conductive particles, conductive paint was prepared in the same manner as in Application Example 3. I got it.
皮較旌止
実施例3の破砕状ポリエチレンを扁平化せずにそのまま
用い、実施例1と同様に銀メッキを施し、導電性粒子を
得た後、応用例1と同様にして導電性塗料を得た。The crushed polyethylene of Skin Comparison Example 3 was used as it is without being flattened, and after silver plating was applied in the same manner as in Example 1 to obtain conductive particles, a conductive paint was applied in the same manner as in Application Example 1. Obtained.
[効 果]
以上応用例1〜3、比較例1〜3について、分散安定性
、導電性について評価を行なった。[Effects] Application Examples 1 to 3 and Comparative Examples 1 to 3 were evaluated for dispersion stability and conductivity.
表 評価結果
分散安定性:室温1週間後の粒子の沈み具合を目視判定
した。Table: Evaluation results Dispersion stability: The degree of settling of the particles was visually determined after one week at room temperature.
0:沈降なし
X:完全に沈降
導 電 性:フィルム上に塗布してその導電性を測定し
た。0: No sedimentation X: Completely sedimentation Conductivity: The film was coated and its conductivity was measured.
O:良好 Δ:やや劣る。O: Good Δ: Slightly inferior.
以上詳細に説明したように、本発明の導電性粒子は分散
安定性が良く1通電性も良好であるので、導電性塗料に
好適なものである。As explained in detail above, the conductive particles of the present invention have good dispersion stability and good current conductivity, so they are suitable for conductive paints.
Claims (1)
/10、厚みの長径の1/2〜1/50の範囲にある扁
平状微小樹脂粉に金属メッキしたことを特徴とする導電
性粒子。The average particle diameter is 100 μm or less, and the short axis is 1/1 to 1 of the long axis.
/10, conductive particles characterized by metal plating on flat microscopic resin powder having a thickness in the range of 1/2 to 1/50 of the major axis.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7787188A JPH01247501A (en) | 1988-03-30 | 1988-03-30 | Electrically conductive particles |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7787188A JPH01247501A (en) | 1988-03-30 | 1988-03-30 | Electrically conductive particles |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01247501A true JPH01247501A (en) | 1989-10-03 |
Family
ID=13646118
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP7787188A Pending JPH01247501A (en) | 1988-03-30 | 1988-03-30 | Electrically conductive particles |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01247501A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6906427B2 (en) | 1997-04-17 | 2005-06-14 | Sekisui Chemical Co., Ltd. | Conductive particles and method and device for manufacturing the same, anisotropic conductive adhesive and conductive connection structure, and electronic circuit components and method of manufacturing the same |
US7045050B2 (en) | 2001-07-31 | 2006-05-16 | Sekisui Chemical Co., Ltd. | Method for producing electroconductive particles |
-
1988
- 1988-03-30 JP JP7787188A patent/JPH01247501A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6906427B2 (en) | 1997-04-17 | 2005-06-14 | Sekisui Chemical Co., Ltd. | Conductive particles and method and device for manufacturing the same, anisotropic conductive adhesive and conductive connection structure, and electronic circuit components and method of manufacturing the same |
US7045050B2 (en) | 2001-07-31 | 2006-05-16 | Sekisui Chemical Co., Ltd. | Method for producing electroconductive particles |
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