TWI253457B - Electroconductive resin composition and electronic parts using the same - Google Patents

Electroconductive resin composition and electronic parts using the same Download PDF

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Publication number
TWI253457B
TWI253457B TW091124102A TW91124102A TWI253457B TW I253457 B TWI253457 B TW I253457B TW 091124102 A TW091124102 A TW 091124102A TW 91124102 A TW91124102 A TW 91124102A TW I253457 B TWI253457 B TW I253457B
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Taiwan
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silver
group
powder
copper powder
plated copper
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TW091124102A
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Chinese (zh)
Inventor
Takehiro Shimizu
Hidekazu Matsuura
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Hitachi Chemical Co Ltd
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    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B1/00Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
    • H01B1/20Conductive material dispersed in non-conductive organic material
    • H01B1/22Conductive material dispersed in non-conductive organic material the conductive material comprising metals or alloys

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  • Physics & Mathematics (AREA)
  • Chemical & Material Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Conductive Materials (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

An electroconductive resin composition which comprises a silver-plated cooper powder (a1) having an aspect ratio of 1 to 20, an electroconductive powder containing a silver powder (A1), a thermoplastic resin (B1) having one or more functional groups selected from the group consisting of an amide group, an ester group, an imide group and en ether group, and an organic solvent (C); an electroconductive resin composition which comprises a silver-plated cooper powder (a2) having cooper exposed on a part of the surface thereof, an electroconductive powder (A2) containing a silver powder, the above thermoplastic resin (B1), and an organic solvent (C); an electroconductive resin composition which comprises the electroconductive powder (A1), a thermoplastic resin (B2) selected from the group consisting of a polyamide silicone resin, a polyamideimide silicone resin and a polyimide silicone resin, and an organic solvent (C); and an electroconductive resin composition which comprises the above electroconductive powder (A2), the above thermoplastic resin (B2) and an organic solvent (C).

Description

1253457 Μ ___ Β7 — - - - I - , . ——- — —— 五、發明説明(1) 發明所屬之技術領域 本發明係有關導電性樹脂組成物及使用其之電子零件 〇 (請先閱讀背面之注意事項再填寫本頁) 先前技術 一般電子零件領域中,於樹脂中混練以金屬爲首之導 電性物質而得的膏狀樹脂組成物,係利用於電路或電極形 成用。其中又以銀爲最具代表性之導電性物質,但,高濕 度條件下負荷電壓時,非常容易離子化,而時有稱爲遷移 之銀移動現象。又,產生遷移時會造成電極間短路,而成 爲電子零件耐濕信賴性降低之原因。 曾檢討添加鎳粉末、鈀粉末或銅粉末以取代銀粉,或 添加各種添加劑,但,任何一種情形就提高電極材料用之 電阻値等而言均寄望改良。 特開平2- 2830 1 0號公報及特開平6-15 1261號公報曾揭示 ,防止固體電解電容器產生遷移之先前技術。 經濟部智慧財產局員工消費合作社印製 發明內容 發明揭示 本發明第一方面係提供,含有含長寬比1至20之鍍銀銅 粉(a 1 )及銀粉的導電性粉末(A 1 ),及具有醯胺基、酉旨 基、醯亞胺基及醚基群中所選出1種以上之官能基的熱證 樹脂(B1 ),及有機溶劑(C )的導電性樹脂組成物(以下 稱爲「組成物K」)。 本紙張尺度適用中國國家標準(CNS ) Α4規格(210Χ297公釐) -4 - 1253457 A7 B7 五、發明説明(2) - - 1 1 Ι^ϋ -I- -i ill e ί·1· I (請先閱讀背面之注意事項再填寫本頁) 本發明第二方面係提供,含有含表面一部分具有銅露 出部分之鍍銀銅粉(a2 )及銀粉的導電性粉末(A2 ),及 具有醯胺基、酯基、醯亞胺基及醚基群中所選出1種以上之 B Hb基的熱塑性樹脂(b 1 ) ’及有機溶劑(C )的導電性樹 組成物(以下稱爲「組成物L」)。 本發明第三方面係提供,含有含長寬比1至2〇之鍍銀銅 粉(a 1 )及銀粉的導電性粉末(A丨),及聚醯胺聚矽氧烷 、聚醯胺醯亞胺聚矽氧烷及聚醯亞胺聚矽氧烷群中所選出 之熱塑性樹脂(B2 ),及有機溶劑(C )的導電性樹脂組成 物(以下稱爲「組成物Μ」)。 本發明第四方面係提供,含有含表面一部分具有銅露 出部分之鍍銀銅粉(a2 )及銀粉的導電性粉末(Α2 ),及 聚醯胺聚矽氧烷、聚醯胺醯亞胺聚矽氧烷及聚醯亞胺聚砂 氧烷群中所選出之熱塑性樹脂(B2 ),及有機溶劑(C )的 導電性樹脂組成物(以下稱爲「組成物N」)。 本發明第五方面係提供,具有使用上述本發明之導電 性樹脂組成物(組成物K、L、Μ、N )而形成的導電體層之 電子零件。 經濟部智慧財產局員工消費合作社印製 發明實施形態 本發明之導電性樹脂組成物爲膏狀樹脂組成物,以下 說明中將單稱爲「組成物」或「膏」。 組成物Κ爲,含有含長寬比1至20之鍍銀銅粉(a 1 )及 銀粉之導電性粉末(A1 ),及具有醯胺基、酯基、醯亞胺 本紙張尺度適用中國國家標準(CNS ) A4規格(2丨〇>< 297公釐) -5- 1253457 A7 B7 經濟部智慧財產局員工消費合作社印製 五、發明説明(3) 基及醚基群中所選出1種以上之官能基的熱塑性樹脂(B1 ) ,及有機溶劑(C )的組成物。使用鱗片狀導電性粉末時, 將其塗布於形狀複雜之部材(多面體)時,邊緣塗覆性將 不足,而會造成電阻力增加及面間電阻偏差,故易使電子 零件產生電特性缺陷,且降低樹脂外裝時之尺寸精準度。 特別是使用於陽極使用閥作用金屬的固體電解電容器之陰 極形成用時,會增加製品漏電流(LC )傾向。相對地,組 成物K具良好塗布性,且乾燥後具良好導電性,又,所得塗 膜於高溫高濕下具優良安定性(耐遷移特性)及尺寸精準 度(邊緣包裹性)。因此,使用組成物K可提供具優良耐濕 信賴性及尺寸精準度的電子零件,例如,將組成物K使用 於陰極形成用時,可提供耐濕信賴性良好且少漏電之固體 電解電容器。 組成物L爲,含有含表面一部分具有銅露出部分之鍍銀 銅粉(a2 )及銀粉的導電性粉末(A2 ),及具有醯胺基、 酯基、醯亞胺基及醚基群中所選出1種以上之官能基的熱塑 性樹脂(B 1 ),及有機溶劑(C )的組成物。目前一般之導 電性粉末係添加銅粉末。此時,電阻値雖優於使用鎳粉或 鈀粉末時,但,隨著銅粉氧化或凝聚合增加膏粘度,而有 經時安定性問題。又,對使用銀粉之導電性膏進行焊接時 ,係利用具焊接機能之粘合用樹脂的熱分解,因此會有塗 膜部分缺損而無法充分接合之問題。另外,先前使用銀粉 及銅粉的導電性膏,會因銀粉與空氣中及粘合用樹脂中所 含的氧起反應,而於表面形成氧化膜,故無法適用於焊接 (請先閲讀背面之注意事項再填寫本頁) 本紙張尺度適用中國國家標準(CNS ) A4規格(210X 297公釐) -6 - 1253457 A7 B7 五、發明説明(4) (請先聞讀背面之注意事項再填寫本頁) 。相對地,組成物L之膏粘度具優良經時安定性,故可形成 能焊接之塗膜。因此’使用組成物L可提供焊接耐熱性優良 之電子零件,例如’將組成物使用於陰極形成用時可提供 ,與抽出陰極部材具優良焊接性,且焊接耐熱性優良之固 體電解電容器。 組成物Μ爲,含有含長寬比1至20之鍍銀銅粉(al )及 銀粉之導電性粉末(A 1 ),及聚醯胺聚矽氧烷、聚醯胺醯 亞胺聚矽氧烷及聚醯亞胺聚矽氧烷群中所選出之熱塑性樹 脂(B2 ),及有機溶劑(C )的組成物。目前,熱硬性樹脂 被廣泛使用爲粘合用膏,但,所得塗膜之塗膜強度及靭性 較差,且形成電路後耐衝擊性較差。又,將該膏使用於固 體電解電容器之電極時,會因塗膜強度及靭性較差,而使 過電壓負荷特性不足。相對地,組成物可形成具優良塗膜 強度及靭性之乾燥塗膜,故使用其特別是可提供過電壓負 荷優良之固體電解電容器等電子零件。 經濟部智慧財產局員工消費合作社印製 組成物N爲,含有含表面一部分具有銅露出部分之鍍銀 銅粉(a2 )及銀粉的導電性粉末(A2 ),及聚醯胺聚矽氧 烷、聚醯胺醯亞胺聚矽氧烷及聚醯亞胺聚矽氧烷群中所選 出之熱塑性樹脂(B2 ),及有機溶劑(C )的組成物。將熱 硬性樹脂作爲粘合用膏時,所得塗膜之撓性較差,因此, 使用於彎曲基板形成電路等,會因彎曲率較大而使塗膜產 生龜裂,而造成短路問題。相對地,組成物N可形成撓性優 良之乾燥塗膜,故使用其特別是可提供耐熱衝擊性優良之 固體電解電容器等電子零件。 -7 - 本紙張尺度適用中國國家標準(CNS ) A4規格(210 X 297公釐) 1253457 A7 B7 經濟部智慧財產局員工消費合作社印製 五、發明説明(5) 組成物K及組成物Μ中,使用含長寬比1至20之鍍銀銅 ( a 1 )及銀粉之導電性粉末(A 1 )。該長寬比係指,鍍 銀銅粉之粒子長徑與短徑比(長徑/短徑)。本發明係以 ’將鍍銀銅粉粒子均混於粘度較低之硬化性樹脂中,靜置 後使粒子沈澱及樹脂硬化,其後切斷所得硬化物之垂直方 向,以顯微鏡觀察剖面所出現之粒子形狀,再一個一個求 取至少1 00個粒子之長徑/短徑而得的平均値爲長寬比。其 中’短徑係指,以二條平行線挾住剖面中出現之粒子外側 時,最短間隔之二條平行線的距離。又,長徑係指,以二 條垂直於短徑的平行線之平行線挾住粒子外側時,最長間 隔之二條平行線的距離,且該四條線所形成的長方形大小 正好可收納粒子。本發明所使用之具體方法如後述。 鍍銀銅粉(a 1 )係指,部分或全部的銅粉表面被覆銀 之導電性粉末。例如,利用取代鍍法、電鍍法、無電解鍍 法等方法,將銀粉被覆於霧狀銅粉上而得。其中又以銅粉 與銀之附著力較高且運轉成本較低之取代鍍法的被覆方法 爲佳。 組成物K中,鍍銀銅粉(a 1 )之銀被覆量並無特別限制 ,就考量導電性及耐遷移性,對銅100重量份較佳爲0.5至50 重量份,更佳爲1.0至35重量份,特佳爲1.5至25重量份。就 膏之塗布性等観點,鑛銀銅粉(a 1 )之長寬比可爲1至2 0。 長寬比超過20時,會使膏之塗布性變差,特別是使用固體 電解電容器之陰極時,會降低元件之邊緣包裹性,而增加 漏電流情形。就考量塗膜導電性等,長寬比較佳爲1.5至18 (請先閲讀背面之注意事項再填寫本頁) 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) -8- 1253457 A7 B7 五、發明説明(6) ,更佳爲2.5至12。就膏之分散性、塗平性、邊緣包裹性及 被膜導電性,鍍銀銅粉(al)之平均粒徑較佳爲0· 2// m至2〇 //m,更佳爲l//m至12//m,特佳爲至8//m。平均粒 徑低於0.2// m時,膏易凝聚,又,超過20// m時,會降低邊 緣包裹性及電阻。該平均粒徑可利用激光散射型流動分布 測定裝置測定。 組成物Μ中,鍍銀銅粉(a 1 )之長寬比可爲1至2 0。言亥 長寬比超過20時,會降低膏之塗布性、導電性塗膜之強度 及靭性,特別是作爲固體電解電容器之陰極用時,會使過 電壓負荷特性變差,而成爲阻抗降低之要因。就考量塗膜 導電性等,該長寬比較佳爲1 · 5至1 8,更佳爲2· 5至1 2。鈹銀 銅粉(a 1 )之銀被覆量並無特別限定,就考量導電性及耐 遷移性,對銅100重量份較佳爲0.5至50重量份,更佳爲1.0 至3 5重量份,更佳爲1.5至2 5重量份。銀被覆量低於1重量份 時,會降低導電性,又,超過30重量份時,會降低電容器 之過電壓負荷特性。就考量膏之分散性、粘度、作業性及 被膜導電性,鍍銀銅粉(al)之平均粒徑較佳爲0.2// m至20 //m,更佳爲l//m至12//m,更佳爲至8//m。平均粒 徑低於0.2//m時,膏易凝聚,又,超過20//m時,會降低塗 布性及電阻。平均粒徑可利用激光散射型流動分布測定裝 置測定。 導電性粉末(A 1 )所含之銀粉並無特別限定,可使用 一般使用的鱗片狀、球狀或塊狀等形狀。就考量導電性、 塗布性及邊緣包裹性,較佳爲鱗片狀及球狀中粒徑爲0.2 本紙張尺度適用中國國家標準(CNS ) A4規格(210X 297公釐) f請先閱讀背面之注意事項再填寫本頁} •壯衣· -訂 經濟部智慧財產局員工消費合作社印製 -9- 1253457 A7 ____ B7 五、發明説明(7) // m至12 // m者,特佳爲1 μ m至8 // m者。 (請先閲讀背面之注意事項再填寫本頁) 導電性粉末(A 1 )中鍍銀銅粉(a 1 )與銀粉比(重量 比)並無特別限制,對鍍銀銅粉(al)丨00重量份之銀粉率 ,就塗膜導電性之觀點,較佳爲25重量份以上,就漏電流 或電容器之過電壓負荷特性觀點,較佳爲400重量份以下, 更佳爲42·8至23 3.3重量份,特佳爲66.6至150重量份。 組成物L及組成物ν中,使用含表面一部分具有銅露出 部分之鍍銀銅粉(a2 )及銀粉的導電性粉末(Α2 )。該鍍 銀銅粉(a2 )爲,部分銅合金粉(即鍍銀銅粉)露出而表 面大略以銀被覆之物。使用鍍銀銅粉之部分銅未露出而全 面以銀被覆之物時,會使組成物之焊接性變差,及使組成 物N之熱衝撃性變差。又,銀粉係提升導電性用,不含銀粉 之組成物不適合導電性層用。 經濟部智慧財產局員工消費合作社印製 鍍銀銅粉(a2 )所使用之銅粉可爲,球狀、鱗片狀、 塊狀、破碎狀等任何形狀,較佳爲霧狀銅粉。就膏粘度之 經時安定性、焊接性、露出部分氧化性、導電性、熱衝撃 性等,鍍銀銅粉(a2)之銅露出面積較佳爲10至70%,更佳 爲10至50%,特佳爲10至30%。銅露出面積可由,測定銀被 覆面積後,與銅粉之表面積的差求得。 鍍銀銅粉(a2 )可利用取代鍍法、電鍍法、無電解鍍 法等方法,將銀被覆於霧狀銅粉上而得。其中又以能提高 銅粉及銀之附著力及運轉成本較低之取代鍍法被覆爲佳。 銅粉表面之銀被覆量就提升骨粘度之經時安定性、焊 接性、成本、導電性等觀點,對銅粉100重量份較佳爲5至 -10 - 本紙張尺度適用中國國家標準(CNS ) A4規格(210X29?公釐) 1253457 A7 B7 五、發明説明(8) 25重量%,特佳爲10至23重量%。 (請先閱讀背面之注意事項再填寫本頁) 導電性粉末(A2 )所含銀粉並無特定限定,可使用一 般所使用的鱗片狀、球狀及塊狀等形狀。就考量導電性、 塗布性及邊緣包裹性,又以鱗球狀及球狀中粒徑0.2 // m至 1 2 // m者爲佳,特佳爲1 // m至8 // m。 鍍銀銅粉(a2 )與銀粉之混合比率並無特別限制,就 考量導電性,對鍍銀銅粉(a2) 100重量單位之銀粉比率較 佳爲25重量份至266重量份,更佳爲66重量份至150重量份。 減少鍍銀銅粉(a2 )之粉末間接觸點時,易提高所得 塗膜之電阻。又,爲了增加鍍銀銅粉之接觸面積以提高導 電性時,較佳係給予鍍銀銅粉(a2 )衝擊使粒子形狀變形 扁平狀。鍍銀銅粉(a2 )之平均粒徑並無特別限制,就考 量膏之塗布性、分散安定性等,較佳爲1至20 // m,較佳爲1 至1 0 // m。平均粒徑可利用激光散射型流動分布測定裝置測 定。 經濟部智慧財產局員工消費合作社印製 組成物K及組成物作爲粘合用樹脂時,就密合性、塡料 分散性及對有機溶劑之溶解性等觀點,而使用具有醯胺基 、酯基、醯亞胺基及醚基群中所選出1種以上之官能基的熱 塑性樹脂(B 1 )。該熱塑性樹脂(B 1 )可複數種組合使用 c 熱塑性樹脂(B 1 )並無特別限制,但就耐熱性等觀點 ,又以具有芳香環爲佳。就對有機溶劑(C )之溶解性的觀 點,又以具有醚鍵爲佳。例如,主鏈具有伸苯基醚(伸苯 基氧化物)鍵及醯胺鍵之聚伸苯基醚醯胺、主鏈具有伸苯 本紙張尺度適用中國國家標準(CNS ) A4規格(2丨〇><297公釐) -11 - 1253457 A7 B7 五、發明説明(9) 基醚鍵及醯亞胺鍵之聚伸苯基醚醯亞胺、主鏈具有伸苯基 醚鍵及醯胺鍵及醯亞胺鍵之聚伸苯基醚醯胺醯亞胺、主鏈 具有伸苯基鍵及醯胺鍵之聚伸苯基醯胺、主鏈具有伸苯基 鍵及醯亞胺鍵之聚伸苯基醯亞胺、主鏈具有伸苯基鍵及醯 胺鍵及醯亞胺鍵之聚伸苯基醯胺醯亞胺、主鏈具有苯二甲 基鍵及醯胺鍵之聚苯二甲基醯胺、主鏈具有苯二甲基鍵及 醯亞胺鍵之聚苯二甲基醯亞胺、主鏈具有苯二甲基鍵及醯 胺鍵及醯亞胺鍵之聚苯二甲基醯胺醯亞胺等,又以使用其 中1種以上爲佳。又,可另含酯鍵、硫化物鍵等,或以隨意 之取代基取代苯環。 具體而言,熱塑性樹脂(B 1 )較佳爲,具有下列一般 式(I)或(Π)所示重覆單位之樹脂。又,較佳爲同時具 有(I)及(II )之重覆單位的樹脂。 一般式(I):1253457 Μ ___ Β7 — — — — I — , . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Note on the back side. In the field of general electronic components, a paste-like resin composition obtained by kneading a conductive material such as a metal in a resin is used for circuit or electrode formation. Among them, silver is the most representative conductive material. However, when the voltage is applied under high humidity conditions, ionization is very easy, and there is a phenomenon of silver migration called migration. Further, when the migration occurs, a short circuit between the electrodes occurs, which is a cause of a decrease in the moisture resistance of the electronic component. It has been reviewed that nickel powder, palladium powder or copper powder is added in place of silver powder, or various additives are added. However, in any case, it is expected to improve the resistance of the electrode material and the like. A prior art for preventing migration of a solid electrolytic capacitor has been disclosed in Japanese Laid-Open Patent Publication No. Hei. No. Hei. No. Hei. The invention provides a conductive powder (A 1 ) containing silver-plated copper powder (a 1 ) having an aspect ratio of 1 to 20 and silver powder, in the first aspect of the invention. And a heat-resistant resin (B1) having one or more functional groups selected from the group consisting of a mercapto group, an anthracene group, a quinone imine group, and an ether group, and a conductive resin composition of the organic solvent (C) (hereinafter referred to as It is "composition K"). This paper scale applies to Chinese National Standard (CNS) Α4 specification (210Χ297 mm) -4 - 1253457 A7 B7 V. Invention description (2) - - 1 1 Ι^ϋ -I- -i ill e ί·1· I ( Please read the following notes on the back side and fill out this page. The second aspect of the present invention provides a conductive powder (A2) containing silver-plated copper powder (a2) having a copper exposed portion on the surface and a silver powder, and having a guanamine A conductive resin composition (b 1 ) of the organic solvent (C) and a conductive tree composition of the organic solvent (C) selected from the group consisting of a base group, an ester group, an oxime imine group, and an ether group (hereinafter referred to as "the composition" L"). According to a third aspect of the present invention, there is provided a conductive powder (A丨) comprising a silver-plated copper powder (a 1 ) having an aspect ratio of 1 to 2 Å and a silver powder, and a polyamine polyoxyalkylene or a polyamide A thermoplastic resin (B2) selected from the group consisting of an imine polyoxyalkylene and a polyamidene polyoxyalkylene group, and a conductive resin composition of an organic solvent (C) (hereinafter referred to as "composition material"). According to a fourth aspect of the present invention, there is provided a conductive powder (Α2) comprising a silver-plated copper powder (a2) having a copper exposed portion on a surface thereof, and a silver powder, and a polyamine polyoxyalkylene or a polyamidimide poly A thermoplastic resin (B2) selected from the group consisting of a siloxane and a polyamidene polysiloxane group, and a conductive resin composition (hereinafter referred to as "composition N") of the organic solvent (C). According to a fifth aspect of the present invention, there is provided an electronic component comprising a conductor layer formed by using the conductive resin composition (compositions K, L, Μ, N) of the present invention. EMBODIMENT OF THE INVENTION The conductive resin composition of the present invention is a paste-like resin composition, and will be referred to as "composition" or "paste" in the following description. The composition is a conductive powder (A1) containing silver-plated copper powder (a 1 ) and silver powder having an aspect ratio of 1 to 20, and having a mercaptoamine group, an ester group, and a quinone imine. Standard (CNS) A4 specification (2丨〇><297mm) -5- 1253457 A7 B7 Ministry of Economic Affairs Intellectual Property Bureau employee consumption cooperative printing 5, invention description (3) selected from the base and ether group A composition of a thermoplastic resin (B1) having a functional group or more and an organic solvent (C). When a scaly conductive powder is used, when it is applied to a member having a complicated shape (polyhedron), the edge coating property is insufficient, and the resistance force is increased and the resistance between the surfaces is deviated, so that the electronic component is liable to cause electrical property defects. And reduce the dimensional accuracy of the resin exterior. In particular, when a cathode of a solid electrolytic capacitor using a valve action metal is used for the anode, the leakage current (LC) of the product tends to increase. In contrast, the composition K has good coatability and good electrical conductivity after drying, and the resulting coating film has excellent stability (migration resistance) and dimensional accuracy (edge wrapping property) under high temperature and high humidity. Therefore, the use of the composition K can provide an electronic component having excellent moisture resistance and dimensional accuracy. For example, when the composition K is used for cathode formation, a solid electrolytic capacitor having good moisture resistance and low leakage can be provided. The composition L is a conductive powder (A2) containing a silver-plated copper powder (a2) having a copper exposed portion on the surface and a silver powder, and has a mercapto group, an ester group, a quinone imine group, and an ether group. A thermoplastic resin (B 1 ) having one or more functional groups and a composition of the organic solvent (C) are selected. At present, a general conductive powder is a copper powder. At this time, although the resistance 値 is superior to the use of the nickel powder or the palladium powder, the viscosity of the paste increases with the oxidation or coagulation of the copper powder, and there is a problem of stability over time. Further, when the conductive paste using silver powder is welded, the resin for bonding with a soldering function is thermally decomposed, so that the coating film portion is defective and cannot be sufficiently joined. In addition, the conductive paste which previously used silver powder and copper powder reacts with oxygen contained in the air and the resin for bonding, and forms an oxide film on the surface, so it is not suitable for soldering (please read the back side first) Note: Please fill in this page. This paper size is applicable to China National Standard (CNS) A4 specification (210X 297 mm) -6 - 1253457 A7 B7 V. Invention description (4) (Please read the notes on the back and fill in the form) Page). In contrast, the paste viscosity of the composition L has excellent stability over time, so that a coating film which can be welded can be formed. Therefore, the use of the composition L can provide an electronic component having excellent solder heat resistance. For example, a composition can be used for forming a cathode, and a solid electrolytic capacitor having excellent solderability and excellent solder heat resistance can be provided. The composition is a conductive powder (A 1 ) containing silver-plated copper powder (al) and silver powder having an aspect ratio of 1 to 20, and polyamine polyoxyalkylene, polyamidoximine polyoxyl A composition of a thermoplastic resin (B2) selected from the group consisting of an alkane and a polyamidene polyoxyalkylene group, and an organic solvent (C). At present, a thermosetting resin is widely used as a paste for bonding, but the film thickness and toughness of the obtained coating film are inferior, and the impact resistance after forming a circuit is inferior. Further, when the paste is used for an electrode of a solid electrolytic capacitor, the strength and toughness of the coating film are poor, and the overvoltage load characteristics are insufficient. On the other hand, since the composition can form a dry coating film having excellent coating film strength and toughness, it is particularly useful for providing electronic parts such as solid electrolytic capacitors excellent in overvoltage load. The printed composition N of the Intellectual Property Office of the Intellectual Property Office of the Ministry of Economic Affairs contains conductive powder (A2) containing silver-plated copper powder (a2) having a copper exposed portion on the surface and silver powder, and polyamine polyoxyalkylene. A composition of a thermoplastic resin (B2) selected from the group consisting of a polyamidoximine polyoxyalkylene and a polyamidene polyoxyalkylene group, and an organic solvent (C). When the thermosetting resin is used as a paste for adhesion, the obtained coating film is inferior in flexibility. Therefore, when it is used in a curved substrate forming circuit or the like, the coating film is cracked due to a large bending rate, which causes a short circuit problem. On the other hand, since the composition N can form a dry coating film excellent in flexibility, it is particularly useful for providing electronic parts such as solid electrolytic capacitors excellent in thermal shock resistance. -7 - The paper size is applicable to China National Standard (CNS) A4 specification (210 X 297 mm) 1253457 A7 B7 Ministry of Economic Affairs Intellectual Property Bureau employee consumption cooperative printing 5, invention description (5) composition K and composition A conductive powder (A 1 ) containing silver-plated copper ( a 1 ) having an aspect ratio of 1 to 20 and silver powder is used. The aspect ratio means the long diameter to short diameter ratio (long diameter/short diameter) of the particles of the silver plated copper powder. In the present invention, the silver-plated copper powder particles are uniformly mixed in a curable resin having a low viscosity, and after standing, the particles are precipitated and the resin is cured, and then the vertical direction of the obtained cured product is cut and observed by a microscope observation section. The particle shape, and the average length of the long diameter/short diameter of at least one hundred particles is obtained as an aspect ratio. The term 'short diameter' refers to the distance between two parallel lines of the shortest interval when two parallel lines are used to clamp the outside of the particles appearing in the section. Further, the long diameter means a distance between two parallel lines of the longest interval when the parallel lines of two parallel lines perpendicular to the short diameter are caught by the outer side of the particle, and the rectangular shape formed by the four lines is just enough to accommodate the particles. The specific method used in the present invention will be described later. The silver-plated copper powder (a 1 ) refers to a conductive powder in which part or all of the copper powder is coated with silver. For example, silver powder is coated on a matte copper powder by a method such as a substitution plating method, a plating method, or an electroless plating method. Among them, a coating method using a substitution plating method in which the adhesion between copper powder and silver is high and the running cost is low is preferable. In the composition K, the silver coating amount of the silver-plated copper powder (a 1 ) is not particularly limited, and the conductivity and the migration resistance are preferably 0.5 to 50 parts by weight, more preferably 1.0 to 100 parts by weight of copper. 35 parts by weight, particularly preferably 1.5 to 25 parts by weight. The aspect ratio of the mineral silver copper powder (a 1 ) may be from 1 to 20 in terms of the coating properties of the paste. When the aspect ratio exceeds 20, the applicability of the paste is deteriorated, and particularly when the cathode of the solid electrolytic capacitor is used, the edge wrapping property of the element is lowered to increase the leakage current. Considering the conductivity of the film, etc., the length and width are preferably 1.5 to 18 (please read the note on the back and fill out this page). The paper size applies to the Chinese National Standard (CNS) A4 specification (210X297 mm) -8- 1253457 A7 B7 5. Invention description (6), more preferably 2.5 to 12. The average particle diameter of the silver-plated copper powder (al) is preferably from 0·2//m to 2〇//m, more preferably l/, in terms of dispersibility, flatness, edge wrapping property and film conductivity. /m to 12//m, especially preferably to 8//m. When the average particle diameter is less than 0.2/m, the paste tends to aggregate, and when it exceeds 20/m, the edge wrapping property and electrical resistance are lowered. The average particle diameter can be measured by a laser scattering type flow distribution measuring device. In the composition, the silver-plated copper powder (a 1 ) may have an aspect ratio of 1 to 20. When the aspect ratio is more than 20, the coating property of the paste and the strength and toughness of the conductive coating film are lowered, and particularly when used as a cathode of a solid electrolytic capacitor, the overvoltage load characteristic is deteriorated, and the impedance is lowered. The cause. Considering the conductivity of the coating film, the length and width are preferably from 1.5 to 18, more preferably from 2.5 to 12. The silver coating amount of the bismuth silver-copper powder (a 1 ) is not particularly limited, and the conductivity and migration resistance are preferably 0.5 to 50 parts by weight, more preferably 1.0 to 35 parts by weight, per 100 parts by weight of copper. More preferably, it is 1.5 to 25 parts by weight. When the amount of silver coating is less than 1 part by weight, the electrical conductivity is lowered, and when it exceeds 30 parts by weight, the overvoltage load characteristics of the capacitor are lowered. The average particle diameter of the silver-plated copper powder (al) is preferably from 0.2/m to 20 //m, more preferably from 1/m to 12/, considering the dispersibility, viscosity, workability and film conductivity of the paste. /m, more preferably up to 8//m. When the average particle diameter is less than 0.2/m, the paste tends to aggregate, and when it exceeds 20/m, the coating property and electrical resistance are lowered. The average particle diameter can be measured by a laser scattering type flow distribution measuring device. The silver powder contained in the conductive powder (A 1 ) is not particularly limited, and a shape such as a scaly shape, a spherical shape or a block shape which is generally used can be used. Considering conductivity, coating and edge wrapping, it is preferred that the scaly and spherical medium particle size is 0.2. The paper size is applicable to the Chinese National Standard (CNS) A4 specification (210X 297 mm) f Please read the back of the note first. Matters to fill out this page} • Sisters · - Department of Economics, Intellectual Property Bureau, Staff Consumer Cooperatives Printed - 9- 1253457 A7 ____ B7 V. Inventions (7) // m to 12 // m, especially good for 1 μ m to 8 // m. (Please read the precautions on the back and fill out this page.) The ratio of silver-plated copper powder (a 1 ) to silver powder (weight ratio) in conductive powder (A 1 ) is not particularly limited. For silver-plated copper powder (al)丨The silver powder ratio of 00 parts by weight is preferably 25 parts by weight or more from the viewpoint of conductivity of the coating film, and is preferably 400 parts by weight or less, more preferably 42.8%, from the viewpoint of leakage current or overvoltage load characteristics of the capacitor. 23 3.3 parts by weight, particularly preferably 66.6 to 150 parts by weight. In the composition L and the composition ν, a conductive powder (Α2) containing silver-plated copper powder (a2) having a copper exposed portion and a silver powder was used. The silver-plated copper powder (a2) is a part of a copper alloy powder (i.e., silver-plated copper powder) which is exposed and has a silver-coated surface. When a part of the copper of the silver-plated copper powder is not exposed and the entire surface is covered with silver, the weldability of the composition is deteriorated, and the thermal flushing property of the composition N is deteriorated. Further, the silver powder is used for improving conductivity, and the composition containing no silver powder is not suitable for the conductive layer. Printed by the Intellectual Property Office of the Intellectual Property Office of the Ministry of Economic Affairs. The copper powder used in the silver-plated copper powder (a2) may be any shape such as a spherical shape, a scale shape, a block shape or a broken shape, and is preferably a copper powder. The copper exposed area of the silver-plated copper powder (a2) is preferably from 10 to 70%, more preferably from 10 to 50, in terms of stability of the viscosity of the paste, weldability, partial oxidation, conductivity, thermal flushing, and the like. %, especially good 10 to 30%. The area of copper exposure can be determined by measuring the difference between the surface area of the silver and the surface area of the copper powder. The silver-plated copper powder (a2) can be obtained by coating silver on a copper-like copper powder by a method such as a substitution plating method, an electroplating method, or an electroless plating method. Among them, it is better to cover the plating method which can improve the adhesion of copper powder and silver and the lower running cost. The silver coating on the surface of the copper powder enhances the stability of the bone viscosity, weldability, cost, conductivity, etc., preferably 100 to 10 parts by weight of the copper powder. The paper scale applies to the Chinese national standard (CNS). A4 size (210X29? mm) 1253457 A7 B7 V. Description of the invention (8) 25 wt%, particularly preferably 10 to 23 wt%. (Please read the precautions on the back and fill in this page.) The silver powder contained in the conductive powder (A2) is not particularly limited, and the scaly, spherical, and block shapes generally used can be used. Considering conductivity, coating and edge wrapping, it is better to have a spherulitic or spherical medium particle size of 0.2 // m to 1 2 // m, especially preferably 1 // m to 8 // m. The mixing ratio of the silver-plated copper powder (a2) to the silver powder is not particularly limited, and the conductivity is considered. The silver powder ratio of the silver-plated copper powder (a2) is preferably from 25 parts by weight to 266 parts by weight, more preferably 66 parts by weight to 150 parts by weight. When the powder indirect contact of the silver-plated copper powder (a2) is reduced, the resistance of the resulting coating film is easily increased. Further, in order to increase the contact area of the silver-plated copper powder to improve the electrical conductivity, it is preferable to apply a silver-plated copper powder (a2) to cause the particle shape to be flattened. The average particle diameter of the silver-plated copper powder (a2) is not particularly limited, and the coating property, dispersion stability, and the like of the paste are preferably from 1 to 20 // m, preferably from 1 to 10 // m. The average particle diameter can be measured by a laser scattering type flow distribution measuring device. When the composition K and the composition of the Intellectual Property Office of the Intellectual Property Office of the Ministry of Economic Affairs are used as a resin for bonding, the use of a mercapto group or ester is used in terms of adhesion, dispersibility of the material, solubility in an organic solvent, and the like. A thermoplastic resin (B 1 ) in which one or more functional groups are selected from the group consisting of a quinone imino group and an ether group. The thermoplastic resin (B 1 ) may be used in combination of plural kinds. The thermoplastic resin (B 1 ) is not particularly limited, but an aromatic ring is preferred from the viewpoint of heat resistance and the like. In view of the solubility of the organic solvent (C), it is preferred to have an ether bond. For example, the main chain has a phenyl ether (phenylene oxide) bond and a guanamine bond, and the main chain has a stretch paper. The Chinese National Standard (CNS) A4 specification (2丨) 〇><297 mm) -11 - 1253457 A7 B7 V. INSTRUCTION DESCRIPTION (9) Polyether phenyl ether quinone imine of an ether bond and a quinone bond, a phenyl ether bond and a hydrazine in the main chain a poly(phenyl ether) amidoxime imine of an amine bond and a quinone bond, a polyphenyleneamine having a phenyl group bond and a guanamine bond in the main chain, a phenyl group bond and a quinone bond in the main chain a polyphenylene quinone imine, a polyphenylene fluorinated imine having a phenylene bond and a guanidine bond in the main chain, and a benzene dimethyl bond and a guanamine bond in the main chain Benzyl decylamine, polyphenylene quinone imine having a benzene dimethyl bond and a quinone bond in the main chain, polyphenyl having a benzene dimethyl bond, a guanamine bond and a quinone bond in the main chain It is preferred to use one or more of dimethylammonium imine or the like. Further, an ester bond, a sulfide bond or the like may be further contained, or a benzene ring may be substituted with an arbitrary substituent. Specifically, the thermoplastic resin (B 1 ) is preferably a resin having a repeating unit represented by the following general formula (I) or (Π). Further, a resin having a repeating unit of (I) and (II) at the same time is preferred. General formula (I):

R3R3

Y、 (I) (請先閱讀背面之注意事項再填寫本頁) -裝· 訂 ·線 經濟部智懇財產局員工消費合作社印製 (式中’ R1、R2、R3及R4各自獨立爲氫、低級院基、低級院 氧基或鹵原子;X1爲單鍵、-〇-、-S-、-C〇-、-S〇2-、-SO-、 ΗY, (I) (Please read the note on the back and then fill out this page) - Install · Order · Ministry of Economic Affairs Zhizhi Property Bureau employee consumption cooperative printing (in the formula 'R1, R2, R3 and R4 are each independently hydrogen , low-grade courtyard base, low-grade courtyard oxygen or halogen atom; X1 is a single bond, -〇-, -S-, -C〇-, -S〇2-, -SO-, Η

X Η R5 I C—— 或 R6 R5及R6各自獨立爲氫、低級烷基、三氟甲基 氯甲基或 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) -12- 1253457 A7 B7 五、發明説明( 苯基;γ爲 -NH—C-Ar1 —C—NH- 〇 II c 〇〇 II II c c -NH-C-Ar N——A \/ 〇 c II 〇 或 N Ar° N-\/\/ G C II II 〇〇 ;Ar1爲芳香族之2價基;Ar2爲芳香族之3價基;Ar3爲芳香族 之4價基)X Η R5 IC - or R6 R5 and R6 are each independently hydrogen, lower alkyl, trifluoromethyl chloromethyl or this paper scale applicable to China National Standard (CNS) A4 specification (210X297 mm) -12- 1253457 A7 B7 V. Description of the invention (phenyl; γ is -NH-C-Ar1 - C-NH- 〇II c 〇〇II II cc -NH-C-Ar N - A \/ 〇c II 〇 or N Ar° N-\/\/ GC II II 〇〇; Ar1 is an aromatic divalent group; Ar2 is an aromatic trivalent group; Ar3 is an aromatic tetravalent group)

般式(IIGeneral (II

(II) (請先閲讀背面之注意事項再填寫本頁) (式中,R7、R8及R9各自獨立爲低級烷基、低級烷氧基或鹵 原子;s、t及u各自獨立爲取代基數之〇至4的整數;R7、R8及 R9各自爲複數鍵時,可各自相同或不同;X2及X3各自獨立爲-〇-或(II) (Please read the notes on the back and fill out this page) (wherein R7, R8 and R9 are each independently a lower alkyl group, a lower alkoxy group or a halogen atom; and s, t and u are each independently a substituent number Then, an integer of 4; when R7, R8, and R9 are each a plural bond, they may be the same or different; X2 and X3 are each independently -〇- or

R10—C-I11R 經濟部智慧財產局員工消費合作社印製 ;R1()及R11各自獨立爲氫原子、低級烷基、三氟甲基、三氯 甲基或苯基;γ同上述一般式(I)) 一般式(I )及(II )較佳爲,低級烷基、低級烷氧基 、碳數1至4之烷基、碳數1至4之烷氧基。一般式(I)及( Π)之R5、R6、R1Q、R11之苯基可無取代或受甲基、乙基、 磺基等隨意之取代基所取代。 本紙^尺度適用中國國家標準(〇奶)八4規格(210>< 297公釐)'' -13- 1253457 五 A7 B7 、發明説明(11) 一般式(Ο所示重覆單位較佳爲,如下列一般式(III 般,相互以1,4 -位鍵結苯環之物。 R3R10—C-I11R Printed by the Consumers' Cooperative of the Intellectual Property Office of the Ministry of Economic Affairs; R1() and R11 are each independently a hydrogen atom, a lower alkyl group, a trifluoromethyl group, a trichloromethyl group or a phenyl group; γ is the same as the above general formula ( I)) The general formulae (I) and (II) are preferably a lower alkyl group, a lower alkoxy group, an alkyl group having 1 to 4 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms. The phenyl groups of R5, R6, R1Q and R11 of the general formulae (I) and (()) may be unsubstituted or substituted by arbitrary substituents such as methyl, ethyl or sulfo groups. The paper size is applicable to the Chinese national standard (〇奶) 八4 specification (210><297 mm)'' -13- 1253457 five A7 B7, invention description (11) general formula (Ο shows that the repeat unit is preferably , as in the following general formula (III, the benzene ring is bonded to each other at the 1,4 - position. R3

R'R'

RR

-Y— (ΠΙ) R4 一般式(II)所示重覆單位同樣地較佳爲’如下列一般 式(IV)般,相互以1,4-位鍵結苯環之物。-Y - (ΠΙ) R4 The repeating unit represented by the general formula (II) is similarly preferably 'as defined in the following general formula (IV), and the benzene ring is bonded to each other at the 1,4-position.

Y— (IV) (請先閱讀背面之注意事項再填寫本頁) •裝· 具有上述重覆單位之熱塑性樹脂(B1 )可由下列所說 明之酸成分(S ),即,芳香族二羧酸、芳香族三羧酸、芳 香族四羧酸或其反應性酸衍生物與下列所說明之二胺反應 而得。又,酸成分及二胺可各自複數種組合使用。 一般式(I )及(III )所示重覆單位中,二胺較佳爲, 例如使用2,2-雙[4-(4-胺基苯氧基)苯基]丙烷、2,2-雙[3-甲基-4-(4-胺基苯氧基)苯基]丙烷、2,2-雙[4-甲基-4-(4-胺 基苯氧基)苯基]丁烷、2,2-雙[3-甲基-4-(4-胺基苯氧基)苯 基]丁烷、2,2-雙[3,5-二甲基-4-(4-胺基苯氧基)苯基]丁烷 、2,2-雙[3 ’ 5-二溴-4-(4-胺基苯氧基)苯基]丁烷、1,1,1 ,3,3,3-六氟-2,2-雙[3 -甲基-4-(4-胺基苯氧基)苯基]丙 烷、1,1-雙[4-(4-胺基苯氧基)苯基]環己烷、1,1-雙[4-(4-胺基苯氧基)苯基]環戊烷、雙[4-(4-胺基苯氧基)苯基]硕、 、-ιτ 經濟部智慧財產局員工消費合作社印製 本紙張尺度適用中國國家標準(CNS ) Α4規格(210Χ297公釐) -14- 1253457 A7 B7 五、發明説明(θ (請先閲讀背面之注意事項再填寫本頁) 雙[4-(4-胺基苯氧基)苯基]醚、雙[4-(3-胺基苯氧基)苯基]硕 、4,4、羰基雙(p -伸苯基氧基)二苯胺、4,4,-雙(4 -胺基苯 氧基)聯苯等1種以上所形成。其中又以2,2 -雙[4 - (4 -胺基苯 氧基)苯基]丙烷特佳。 一般式(Π )及(IV )所示重覆單位中,二胺較佳爲, 例如使用1,3-雙(3-胺基苯氧基)苯、1,3-雙(4-胺基苯氧基 )苯、1,4-雙(4-胺基苯氧基)苯、4,4,-[1,3-伸苯基雙(1-甲基亞乙基)]雙苯胺、4,4’-[1,4-伸苯基雙(1-甲基亞乙基 )]雙苯胺、3,3’-[1,3-伸苯基雙(1-甲基亞乙基)]雙苯胺等1 種以上所形成。 形成一般式(I) 、(II) 、(III) 、(IV)之重覆單 經濟部智慧財產局員工消費合作社印製 位時,除了上述二胺例示外,可倂用4,4·-二胺基二苯基醚 、4,41-二胺基二苯基甲烷、4,4,-二胺基-3,3,,5,5,-四 甲基一^苯基釀、4’ 4^ 一^胺基-3,3’,5,5·-四甲基二苯基 甲烷、4,4·-二胺基-3,3,,5,5,-四乙基二苯基醚、2,2,-[4,4’-二胺基-3,3’,5,5、四甲基二苯基]丙烷、間苯二胺 、對苯二胺、3,3 二胺基二苯基硕、哌嗪 '六伸甲基二胺 、七伸甲基二胺、四伸甲基二胺、p-二甲苯二胺、m-二甲 苯二胺、二甲苯二胺、3-甲基t伸甲基二胺、1,3-雙(3-胺 基丙基)四甲基二矽氧烷等1種以上。 芳香族二羧酸爲,芳香族環鍵結2個羧基之羧酸。芳香 族三羧酸爲,芳香族環鍵結3個羧基之羧酸,又以3個羧基 中2個鍵結於接鄰之碳原子上爲佳。芳香族四羧酸爲,芳香 族環鍵結4個錢基之竣酸’又以4個竣基中2個鍵結於接鄰之 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐1 1253457 Α7 Β7 經濟部智慧財產局員工消費合作社印製 五、發明説明( 碳原子上爲佳。該芳香環可爲導入雜原子之物(芳香族雜 環),或介由伸烷基、氧、單鍵、羰基等鍵結芳香族環們 。另外,該芳香族環可含有無關烷氧基、烯丙氧基、烷基 胺基、鹵素等之縮合反應的取代基。 芳香族二羧酸如,對苯二甲酸、間苯二甲酸、4,4’-二 苯基醚二羧酸、4,4、二苯基硕二羧酸、4,4·-二苯基二羧 酸、1,5_萘二羧酸等,但以易取得且廉價之對苯二甲酸及 間苯二甲酸爲佳。芳香族二羧酸之反應性衍生物係指,前 述芳香族二羧酸之二氫化物或二溴化物、二酯等。 芳香族三羧酸較佳如,偏苯三酸、3,3’,4-二苯甲酮 三羧酸、,2,3,4’-二苯基三羧酸、2,3,6-吡啶三羧酸、3 ,3,4’-苯醯苯胺三羧酸、1,4,5 -萘三殘酸、2’-氯-3,4, 4 ’ -苯醯苯胺二羧酸等。芳香族三羧酸之反應性衍生物係指 ,前述芳香族三羧酸之酸酐物、鹵化物、酯、醯胺、銨鹽 等。具體例較佳如,偏苯三酸酐、偏苯三酸酐單氯化物、1 ,4-二羧基- 3-N,N-二甲基胺基甲醯苯、i,4-二甲酯基-3-羧基苯、1,4-二羧基-3-苯氧羰基苯、2,6-二羧基-3-甲酯 基吡啶、1,6-二羧基-5 -胺基甲醯萘,前述芳香族三羧酸鹽 類與氨、二甲基胺、三甲基胺等所形成之銨鹽等。其中又 以易取得且廉價之偏苯三酸酐及偏苯三酸酐單氯化物爲佳 〇 芳香族四羧酸較佳如,均苯四酸、3,3,,4,4’-二苯甲 酮四羧酸、3,3’,4,4’-聯苯四羧酸、1 , 2,5,6-萘四羧 酸、2,3,ό,7-萘四羧酸、2,3,5,ό-哦啶四羧酸、1,4 (諳先閱讀背面之注意事項再填寫本頁) 本紙張尺度適用中國國家標準(CNS ) Α4規格(210Χ297公釐) -16- 1253457 Α7 Β7 五、發明説明( ,5,8-萘四羧酸、3,4,9,10-驼四羧酸、4,4,-磺醯二默 酉夂、聯二本_3,3",4,4"-四竣酸、ρ -聯二苯-3,3M ? 4 j 4、_四羧酸、4,4’-氧基二酞酸、i,i,1,3,3,3-六氟、2 (請先閎讀背面之注意事項再填寫本頁} ,2-雙(2,3-二羧基苯基)丙烷、2,2-雙(2,3-二羧基苯基) 丙院、2,2 -雙(3,4 -二竣基苯基)丙院、1,1,1,3,3,3、 六氟-2,2’-雙[4-(2,3-二羧基苯氧基)苯基]丙烷等。芳香族 四羧酸之反應性衍生物係指,前述芳香族四羧酸之酸二酐 、鹵化物、酯、醯胺、銨鹽等。 芳香族二羧酸、芳香族三羧酸、芳香族四羧酸或其反 應性衍生物所形成的酸成分(S )之使用量,就所得聚合物 之分子量、機械強度、耐熱性等觀點,對二胺總量i 00莫耳 %較佳爲,總量80至120莫耳%,特佳爲95至1〇5莫耳。/〇。 組成物Μ及組成物N作爲粘合用樹脂時,就提升所形成 之塗膜的耐熱性及低彈性率化等觀點,所使用之熱塑性樹 月旨(Β 2 )爲,聚醯胺聚矽氧樹脂、聚醯胺醯亞胺樹脂及聚 醯亞胺聚矽氧樹脂中所選出。該熱塑性樹脂(Β 2 )可複數 種組合使用。 經濟部智慧財產局員工消費合作社印製 該熱塑性樹脂(Β 2 )並無特別限制,例如可使芳香族 二羧酸、芳香族三羧酸、芳香族四羧酸或其反應性衍生物 等酸成分與’以一胺基聚砂氧院爲必須成分的二胺聚縮合 而得。 所使用之二胺基聚矽氧烷較佳如, 本紙張尺度適用中國國家標準(CNS ) Α4規格(210Χ297公釐) -17- 1253457 A7 B7 五、發明説明(1Y— (IV) (Please read the precautions on the back and fill out this page) • Packing · The thermoplastic resin (B1) having the above repeated unit can be the acid component (S) described below, ie, aromatic dicarboxylic acid An aromatic tricarboxylic acid, an aromatic tetracarboxylic acid or a reactive acid derivative thereof is obtained by reacting a diamine as described below. Further, the acid component and the diamine may be used in combination of plural kinds. In the repeating unit represented by the general formulae (I) and (III), the diamine is preferably, for example, 2,2-bis[4-(4-aminophenoxy)phenyl]propane, 2,2- Bis[3-methyl-4-(4-aminophenoxy)phenyl]propane, 2,2-bis[4-methyl-4-(4-aminophenoxy)phenyl]butane 2,2-bis[3-methyl-4-(4-aminophenoxy)phenyl]butane, 2,2-bis[3,5-dimethyl-4-(4-amino) Phenoxy)phenyl]butane, 2,2-bis[3' 5-dibromo-4-(4-aminophenoxy)phenyl]butane, 1,1,1,3,3, 3-hexafluoro-2,2-bis[3-methyl-4-(4-aminophenoxy)phenyl]propane, 1,1-bis[4-(4-aminophenoxy)benzene Cyclohexane, 1,1-bis[4-(4-aminophenoxy)phenyl]cyclopentane, bis[4-(4-aminophenoxy)phenyl], , Ιτ Ministry of Economic Affairs Intellectual Property Bureau Employees Consumption Cooperatives Printed on this paper scale Applicable to China National Standard (CNS) Α4 Specifications (210Χ297 mm) -14- 1253457 A7 B7 V. Invention Description (θ (Please read the back note first and then fill in This page is bis[4-(4-aminophenoxy)phenyl]ether, bis[4-(3-aminophenoxy)phenyl], 4,4, carbonyl One or more kinds of (p-phenylphenyloxy)diphenylamine and 4,4,-bis(4-aminophenoxy)biphenyl are formed, and 2,2-bis[4 - (4 - Aminophenoxy)phenyl]propane is particularly preferred. In the repeating units represented by the formulae (Π) and (IV), the diamine is preferably, for example, 1,3-bis(3-aminophenoxy). Benzene, 1,3-bis(4-aminophenoxy)benzene, 1,4-bis(4-aminophenoxy)benzene, 4,4,-[1,3-phenylene bis( 1-methylethylidene)]diphenylamine, 4,4'-[1,4-phenylenebis(1-methylethylidene)]diphenylamine, 3,3'-[1,3-stretch One or more kinds of phenylbis(1-methylethylidene)]diphenylamine are formed. The employees of the Intellectual Property Bureau of the Ministry of Economics, which form the general formula (I), (II), (III), and (IV) When the consumer cooperative prints the position, in addition to the above diamines, 4,4·-diaminodiphenyl ether, 4,41-diaminodiphenylmethane, 4,4,-diamino group can be used. -3,3,,5,5,-tetramethyl-phenyl, 4' 4^-amino-3,3',5,5-tetramethyldiphenylmethane, 4,4 ·-Diamino-3,3,,5,5,-tetraethyl Phenyl ether, 2,2,-[4,4'-diamino-3,3',5,5, tetramethyldiphenyl]propane, m-phenylenediamine, p-phenylenediamine, 3,3 Diaminodiphenyl, piperazine 'hexamethyldiamine, heptamethyldiamine, tetramethylamine, p-xylylenediamine, m-xylenediamine, xylenediamine One or more kinds of 3-methyl t-methyldiamine and 1,3-bis(3-aminopropyl)tetramethyldioxane. The aromatic dicarboxylic acid is a carboxylic acid in which two carboxyl groups are bonded to an aromatic ring. The aromatic tricarboxylic acid is a carboxylic acid in which an aromatic ring is bonded to three carboxyl groups, and it is preferred that two of the three carboxyl groups are bonded to the adjacent carbon atom. The aromatic tetracarboxylic acid is an aromatic ring bonded with 4 krafts of citric acid, and 2 of the 4 thiol groups are bonded to the adjacent paper. The Chinese National Standard (CNS) A4 specification (210X297) PCT 1 1253457 Α7 Β7 Ministry of Economic Affairs Intellectual Property Bureau employee consumption cooperative printing 5, invention description (carbon atom is preferred. The aromatic ring can be introduced into the hetero atom (aromatic heterocyclic ring), or through the alkyl group, oxygen The aromatic ring may be bonded to a single bond, a carbonyl group, etc. The aromatic ring may contain a substituent which is not related to a condensation reaction such as an alkoxy group, an allyloxy group, an alkylamino group or a halogen. For example, terephthalic acid, isophthalic acid, 4,4'-diphenyl ether dicarboxylic acid, 4,4, diphenyl terephthalic acid, 4,4·-diphenyldicarboxylic acid, 1 5 - naphthalene dicarboxylic acid, etc., but preferably available and inexpensive terephthalic acid and isophthalic acid. The reactive derivative of the aromatic dicarboxylic acid means the dihydrogenation of the aforementioned aromatic dicarboxylic acid Or dibromide, diester, etc. The aromatic tricarboxylic acid is preferably, for example, trimellitic acid, 3,3',4-benzophenone tricarboxylic acid, , 2,3,4'-diphenyltricarboxylic acid, 2,3,6-pyridinetricarboxylic acid, 3,3,4'-benzoanilide tricarboxylic acid, 1,4,5-naphthalene tris And 2'-chloro-3,4,4'-benzoquinone dicarboxylic acid, etc. The reactive derivative of the aromatic tricarboxylic acid means an anhydride, a halide, an ester, and an anthracene of the aromatic tricarboxylic acid. Amine, ammonium salt, etc. Specific examples are, for example, trimellitic anhydride, trimellitic anhydride monochloride, 1, 4-dicarboxy-3-N,N-dimethylaminomethylhydrazine, i,4-dimethyl ester- 3-carboxybenzene, 1,4-dicarboxy-3-phenoxycarbonylbenzene, 2,6-dicarboxy-3-carbomethoxypyridine, 1,6-dicarboxy-5-aminocarbazinyl, the aforementioned aromatic An ammonium salt formed by a tricarboxylic acid salt, an ammonia, a dimethylamine or a trimethylamine, etc., wherein an easily obtained and inexpensive trimellitic anhydride and a trimellitic anhydride monochloride are preferred. For example, pyromellitic acid, 3,3,4,4'-benzophenone tetracarboxylic acid, 3,3',4,4'-biphenyltetracarboxylic acid, 1, 2,5,6-naphthalene Tetracarboxylic acid, 2,3,anthracene,7-naphthalenetetracarboxylic acid, 2,3,5,indole-omega tetracarboxylic acid, 1,4 Note on this page. This paper size applies to Chinese National Standard (CNS) Α4 specification (210Χ297 mm) -16- 1253457 Α7 Β7 5. Invention description (5,8-naphthalenetetracarboxylic acid, 3,4, 9,10-Camel tetracarboxylic acid, 4,4,-sulfonate, bismuth, bis, _3,3",4,4"-tetradecanoic acid, ρ-biphenyl-3,3M ? 4 j 4, _ tetracarboxylic acid, 4,4'-oxydicyric acid, i, i, 1,3,3,3-hexafluoro, 2 (please read the back of the note first, then fill out this page), 2-bis(2,3-dicarboxyphenyl)propane, 2,2-bis(2,3-dicarboxyphenyl)propyl, 2,2-bis(3,4-diphenyl)propyl Home, 1,1,1,3,3,3, hexafluoro-2,2'-bis[4-(2,3-dicarboxyphenoxy)phenyl]propane, etc. The reactive derivative of the aromatic tetracarboxylic acid means an acid dianhydride, a halide, an ester, a decylamine or an ammonium salt of the above aromatic tetracarboxylic acid. The amount of the acid component (S) formed by the aromatic dicarboxylic acid, the aromatic tricarboxylic acid, the aromatic tetracarboxylic acid or a reactive derivative thereof is based on the molecular weight, mechanical strength, and heat resistance of the obtained polymer. The total amount of the diamines i 00 mol% is preferably from 80 to 120 mol%, particularly preferably from 95 to 1.5 mol. /〇. When the composition Μ and the composition N are used as a resin for bonding, the heat resistance and the low modulus of elasticity of the formed coating film are improved, and the thermoplastic tree used (Β 2 ) is a polyamine polycondensation. Oxygen resin, polyamidoximine resin and polyamidene polyoxyl resin are selected. The thermoplastic resin (Β 2 ) can be used in combination of plural kinds. The thermoplastic resin (Β 2 ) printed by the Intellectual Property Office of the Intellectual Property Office of the Ministry of Economic Affairs is not particularly limited. For example, an acid such as an aromatic dicarboxylic acid, an aromatic tricarboxylic acid, an aromatic tetracarboxylic acid or a reactive derivative thereof may be used. The composition is obtained by polycondensation of a diamine which is an essential component of an amine-based polyoxan. The diamine-based polyoxane used is preferably, for example, the Chinese National Standard (CNS) Α4 specification (210Χ297 mm) -17- 1253457 A7 B7. The invention description (1)

Yl I N H2Yl I N H2

H2 N 1Y— 2I-2 Y—s—V (式中,Y爲2價烴基,γ2爲一價烴基,又,2個γ1可相同或 相異,複數個Υ可相同或相異,m爲i以上之整數)所示之 物。 Y1所示之2價烴基如,碳數1至1〇之伸烷基、取代或無 取代之伸苯基等,Y2所示一價烴基如,碳數1至1〇之烷基、 取代或無取代之苯基等,m較佳爲1至1〇〇之整數。該二胺基 聚矽氧烷可單用或2種以上組用。 能與上述二胺基聚矽氧烷共用之其他二胺並無特別限 制’但就樹脂之耐性、對有機溶劑之溶解性及溶解粘度等 觀點,又以使用芳香族二胺爲佳,更佳爲使用主鏈含有伸 苯基醚之聚伸苯基醚二胺。 具體而言,以使用下列一般式(VI )所示芳香族二胺 爲佳。 h2n、 (請先閱讀背面之注意事項再填寫本頁) 裝· 訂 I·線 經濟部智慧財產局員工消費合作社印製H2 N 1Y— 2I-2 Y—s—V (wherein Y is a divalent hydrocarbon group, γ2 is a monovalent hydrocarbon group, and further, two γ1s may be the same or different, and plural Υ may be the same or different, m is i is an integer shown above). The divalent hydrocarbon group represented by Y1 is, for example, an alkylene group having 1 to 1 Å, a substituted or unsubstituted phenyl group, and the like, and a monovalent hydrocarbon group represented by Y2, for example, an alkyl group having 1 to 1 Å, a substitution or The unsubstituted phenyl group or the like, m is preferably an integer of from 1 to 1 Å. The diaminopolyoxyalkylene oxide may be used singly or in combination of two or more. The other diamine which can be used in common with the above diamine-based polyoxane is not particularly limited, but it is preferable to use an aromatic diamine from the viewpoints of resistance to a resin, solubility to an organic solvent, and solubility. In order to use a polyphenylene ether diamine containing a pendant phenyl ether in the main chain. Specifically, it is preferred to use the aromatic diamine represented by the following general formula (VI). H2n, (please read the precautions on the back and fill out this page) Packing and Booking I·Line Printed by the Intellectual Property Office of the Ministry of Economic Affairs

nh2 (VI) 中,R1、R2、R3及R4各自獨立爲氫、碳數1至4之烷基、 玫1至4之烷氧基或鹵原子;χ1爲單鍵、-〇-、_s_、-co· SOo- > -SO- ' 本紙張尺度適财酬家標準(CNS ) A4規格(2lGX 297公釐) -18- 1253457 A7 B7 五、發明説明(βIn nh2 (VI), R1, R2, R3 and R4 are each independently hydrogen, an alkyl group having 1 to 4 carbon atoms, an alkoxy group of 1 to 4 or a halogen atom; χ1 is a single bond, -〇-, _s_, -co· SOo- > -SO- ' This paper scales the appropriate standard (CNS) A4 specifications (2lGX 297 mm) -18- 1253457 A7 B7 V. Invention description (β

;R5及R6各自獨立爲氫、碳數1至4之低級烷基、三氟甲基 三氯甲基、取代或無取代之苯基)。 一般式(VI )之聚伸苯基醚二胺較佳如下列一般式 VII )所示般,相互以Μ-位鍵結苯環之物。 η2νR5 and R6 are each independently hydrogen, a lower alkyl group having 1 to 4 carbon atoms, a trifluoromethyltrichloromethyl group, a substituted or unsubstituted phenyl group). The polyphenylene diamine of the general formula (VI) is preferably bonded to the benzene ring at the Μ-position as shown by the following general formula VII). Η2ν

(請先閲讀背面之注意事項再填寫本頁) (VII) 經濟部智慧財產局員工消費合作社印製 一般式(VII )所示具有醚鍵之芳香族二胺(e 1 )如,2 ,2-雙[4-(4-胺基苯氧基)苯基]丙烷、2,2-雙[3-甲基-4-(4-胺基苯氧基)苯基]丙烷、2,2-雙[4_(4-胺基苯氧基)苯基]丁 烷、2,2-雙[3 -甲基- 4-(4-胺基苯氧基)苯基]丁烷、2,2-雙 [3,5-二甲基-4-(4-胺基苯氧基)苯基]丁烷、2,2-雙[3,5-二溴-4-(4-胺基苯氧基)苯基]丁烷、1,1,1,3,3,3-六 氟-2,2-雙[3 -甲基-4-(4-胺基苯氧基)苯基]丙烷、1,1_雙μ-Η-胺基苯氧基) 苯基] 環 己烷、 1 , 1-雙 [4-(4-胺基苯氧基) 苯 基]環戊烷、雙[4-(4-胺基苯氧基)苯基]硕、雙[4-(4-胺基苯 氧基)苯基]醚、雙[4-(3-胺基苯氧基)苯基]硕、4,4’-羰基雙 (P-伸苯基氧基)二苯胺、4,4’-雙(4-胺基苯氧基)聯苯等,又 ,可單用或組用。其中較佳爲2,2-雙[(4-胺基苯氧基)苯基] 丙院。 本紙張尺度適用中國國家標準(CNS ) A4規格(210X 297公釐) -19- 1253457 A7 B7 五、發明説明(1乃 除了上述(el )之芳香族二胺(e2 )如,1,3-雙(3-胺 基苯氧基)苯、1,3-雙(4-胺基苯氧基)苯、1,4-雙(4-胺基苯 氧基)苯、4,4’-[1,3-伸苯基雙(1-甲基亞乙基)]雙苯胺、4 ,4,-[1,4-伸苯基雙(1-甲基亞乙基)]雙苯胺、3,3,-[1,3-伸苯基雙(1-甲基亞乙基)]雙苯胺、4,4,-二胺基苯基醚、4 ,4·-二胺基二苯基甲烷、4,4、二胺基-3,3,,5,5|_四甲 基二苯基醚、4,4、二胺基-3,3,,5,5,_四甲基二苯基甲 烷、4,4’-二胺基-3,3’,5,5'-四乙基二苯基醚、2,2-[4 ,4’-二胺基-3,3,,5,5’-四甲基二苯基]丙烷、間苯二胺 、對苯二胺、3,3·-二胺基二苯基碾、〇_二甲苯二胺、 甲苯二胺、p -二甲苯二胺等,又,可單用或組用。 除了上述(el )及(e2 )之二胺,即脂肪族或脂環式 二胺(e3 )如,哌嗪、六伸曱基二胺、七伸甲基二胺、四 伸甲基二胺、3_甲基t伸甲基二胺等,又,可單用或組用。 合成熱塑性樹脂(B2 )時,與以上述二胺基聚矽氧烷 爲必須成分之二胺反應的酸成分可爲,上述合成樹脂(B 1 )用之上述酸成分(S )。該芳香族二羧酸、芳香族三羧酸 、芳香族四羧酸或其反應性衍生物所形成的酸成分(S )之 使用量,就所得聚合物之分子量、機械強度、耐熱性等觀 點,對二胺總量100莫耳%較佳爲,總量80至120莫耳%,特 佳爲9 5至1 0 5莫耳%。 組成物K中,導電性粉末C AD與熱塑性樹脂(B 1 )之混 合比率並無限定,但就所形成之塗膜的導電性等觀點,對 (A1)成分1〇〇重量份之(B1)成分較佳爲2至25重量份, 本紙張尺度適用中國國家標準(CNS ) Α4規格(210Χ 297公釐) —.---.---^---- (請先閲讀背面之注意事項再填寫本頁) 、1Τ 經濟部智慧財產局員工消費合作社印製 -20- 1253457 A7 __B7_ 五、發明説明(1弓 更佳爲4至14重量份。 組成物(Μ )中,導電性粉末(A1 )與熱塑性樹脂( Β2 )之混合比率並無限定,但就塗膜強度、韌性及導電性 等觀點,對(Α1 )成分100重量份之(Β2 )成分較佳爲2至 25重量份,特佳爲4至14重量份。 組成物Ν中,導電性粉末(Α2)與熱塑性樹脂(Β2)之 混合比率並無限定,但就塗膜之撓性、導電性等觀點,(Α2 )成分100重量份之(Β2)成分較佳爲2至25重量份,更佳 爲4至1 4重量份。 組成物Κ、L、Μ、Ν所使用之有機溶劑(C )如,苯、 甲苯、二甲苯等芳香族溶劑;丙酮、甲基乙基酮、甲基異 丁基酮、環己酮等酮系溶劑;二乙基醚、異丙基醚、四氫 呋喃、二噁烷、乙二醇二甲基醚、乙二醇二乙基醚、二乙 二醇二甲基醚、二乙二醇二乙基醚等醚系溶劑;乙酸乙酯 乙酸-η-丙酯、乙酸異丙酯、乙酸-η-丁酯、乙二醇單甲基醚 乙酸酯、乙二醇單乙基醚乙酸酯、乙二醇單丁基醚乙酸酯 、二乙二醇單甲基醚乙酸酯、二乙二醇單甲基醚乙酸酯、 丙二醇單甲基醚乙酸酯、丙二醇單甲基醚乙酸酯、丙二醇 單乙基醚乙酸酯、r -丁內酯等酯系溶劑;二甲基甲醯胺、 二甲基乙醯胺、N-甲基吡咯烷酮等醯胺系溶劑。該溶劑係 作爲製作膏時溶解樹脂或調整膏之粘度用,又,可單用或2 種以上組用。 有機溶劑(C )之添加量就樹脂之溶解性、膏之粘度、 導電性粉末之分散性及塗膜形成性等觀點,對熱塑性樹脂 (請先閲讀背面之注意事項再填寫本頁) 裝_ 訂 經濟部智慧財產局員工消費合作社印製 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) -21 - 1253457 A7 B7 五、發明説明(1弓 iOO重量份一般爲75至46〇0重量份,較佳爲I25至3〇60重量 份。 (請先閱讀背面之注意事項再填寫本頁) 含上述添加成分之各組成物例如可利用萊卡機、3座滾 軸機、球磨機、分散機等,將各成分混練分散而得。又, 爲了提升導電性粉末(塡料)之分散性及塗布性,可添加 分散劑或偶合劑。 所使用之分散劑較佳如,碳數16至20之棕櫚酸、硬脂 酸等飽和脂肪酸;碳數16至18之油酸、亞油酸等不飽和脂 肪酸;該飽和/不飽和脂肪酸之鈉、鉀、鈣、鋅、銅等金 屬鹽中1種以上。分散劑添加量就導電性粉末之分散性、塗 膜之導電性、塗膜與基材之密合性等觀點,對樹脂1 00重量 份較佳爲0.2至240重量份,更佳爲2至120重量份。 經濟部智慧財產局員工消費合作社印製 偶合劑如,乙烯基甲氧基矽烷、乙烯基三乙氧基矽烷 、乙烯基三(/3 -甲氧基乙氧基)矽烷、/3 -(3,4_環氧基環己 基)乙基三甲氧基矽烷、r-環氧丙氧基丙基三甲氧基矽烷、 r-環氧丙氧基丙基三甲氧基矽烷、r-環氧丙氧基丙基甲基 二乙氧基矽烷、N- /3 -(胺基乙基)-r -胺基丙基甲基二甲氧 基矽烷、r-胺基丙基三乙氧基矽烷、N-苯基胺基丙基 .三甲氧基矽烷、r -锍基丙基三甲氧基矽烷等矽烷偶合劑, 或鈦酸酯系偶合劑、鋁酸酯系偶合劑、鍩鋁酸酯系偶合劑 等,其對上述熱塑性樹脂1 〇 〇重量份之添加量較佳爲3 〇重量 份以下。 本發明之組成物適用於各種電子零件之導電體層,例 如導電電路或電極材料。 本紙張尺度適用中國國家標準(CNS ) A4規格(210X29?公釐) -22- 1253457 A7 B7 五、發明説明(2() (請先閲讀背面之注意事項再填寫本頁) 本發明之電子零件爲,具有使用本發明組成物所形成 之導電體層。各種電子零件如,以該組成物爲電極材料之 鋁電解電容器、鉅固體電解電容器、陶瓷電容器等;利用 網版印刷由本發明組成物形成導電電路之各種基板;以本 發明組成物所形成之導電電路作爲天線用電路的1C卡等。 本發明組成物亦適用爲,陽極使用閥作用金屬之固體電解 電容器的陰極材料。 本發明之電子零件較佳爲,由閥作用金屬所形成之陽 極基體J:,形成含有電介質氧化膜、固體電解質層及使用 本發明組成物而形成的導電體層之陰極層的固體電解電容 器。 經濟部智慧財產局員工消費合作社印製 圖1所示之例的固體電解電容器10具備,含有埋設陽極 線1之陽極基體2,及依序形成於陽極基體2上之電介質氧膜 (陽極氧化被膜)3,及固體電解質層(半導體層)4,及 碳層51與導電體層5 2所構成之陰極5的電容器元件。陽極基 體2所使用之閥作用金屬較佳爲鉬、鋁、鈦、鈮等。陽極基 體2之形狀較佳爲箔狀、板狀或棒狀。該陽極基體2之形成 方法爲’以埋設钽導線等之陽極線1形態,將閥作用金屬粉 末壓縮成型後,真空中以2000 °C加熱數10分鐘而成爲燒結 體。 其次,於硝酸或磷酸等化成液中,對所得燒結體(陽 極基體2 )施加電壓,化成後於陽極基體2表面上形成Ta2〇3 等之電介質氧化膜3。該氧化膜較佳爲,陽極基體金屬本身 之氧化物所形成的層,但可爲不同於陽極基體之電介質氧 ^紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) ~ ' 1253457 A7 B7 五、發明説明(21) (請先閲讀背面之注意事項再填寫本頁) 化物層。形成電介質氧化膜後,將燒結體浸漬於硝酸錳溶 液等半導體母液中,含浸液體後以2〇〇至3 5〇 π燒成熱分解 ’而於燒結體內部(燒結體表面)形成以二氧化錳層爲主 之固體電解質層4。熱分解後再化成以修復燒結時損傷之電 介質氧化膜3 °必要時重覆5至10次以上之浸漬、燒成及再 化成步驟’以形成所需厚度之固體電解質層4。又,該固體 電解質層可使用稱爲有機半導體之TCNQ ( 7,7,8,-四氰 基D奎啉并二甲焼)錯合物或導電性高分子之聚吡咯、聚噻 吩、聚苯胺等形成。 形成固體電解質層4後,塗布碳膏,乾燥後形成陰極層 5 —部分的碳層5 1,接著利用本發明組成物於其上形成陰極 層另一部分之導電體層(銀層或銀膏層)5 2。利用焊接或 導電性接著劑6等,將取出陰極用之導線框7接連於所得導 電體層52 ’另外將由燒結體2引出的陽極線丨熔接於導線框7 等。最後利用樹脂浸漬法或樹脂塑模法等,以外裝樹脂整 體密封。所得之固體電解電容器尺寸一般爲,長2至7111111、 莧 1.25至 4.3mm、局 1.2至 2.8mm。 經濟部智慧財產局員工消費合作社印製 下面將以實施例更詳細說明本發明,又,實施例中各 種特性之測定方法及評估方法如下所示。 [長寬比] 混合低粘度環氧樹脂(繆拉公司製)之主劑(N 〇.丄〇 _ 8130) 8g及硬化劑(ν〇·10-8132) 2g後,加入測定用粉體2g ’充分分散後以30°C真空脫泡,3(TC下靜置1〇小時以使粒 本紙張尺度適用中國國家標準(CNS ) A4規格(210X 297公釐) -24- 1253457 A7 B7 五、發明説明(2弓 子沈澱、樹脂硬化。其後以垂直方向切斷所得硬化物’再 利用顯微鏡以1000倍觀察剖面,並求取剖面所出現150個粒 子之長徑/短徑,再以其平均値爲長寬比。 [平均粒徑] 利用馬斯達分粒器(馬魯曼公司製)測定粉體平均粒 徑。 [銅露出面積] 隨意取出5個製得之鍍銀銅粉粒子,利用掃描型奧格電 子分光分析裝置觀察,並由奧格像進行貴金屬(銀)及非 貴金屬(銅)的定量分析,計算銅佔有率後,以測定用5個 之平均値作爲銅露出面積(% )。 [膏粘度] 恒溫層內溫度設定爲25 °C下,利用東京計器製E型粘度 計3° cone測定,並以開始測定至1〇分鐘後之値爲膏粘度。 (請先閱讀背面之注意事項再填寫本頁) -------m --.....I------ n :―I·- -裝·(Please read the precautions on the back and fill out this page.) (VII) The Ministry of Economic Affairs, Intellectual Property Office, Staff Consumer Cooperative, printed the aromatic diamine (e 1 ) with an ether bond as shown in general formula (VII). - bis[4-(4-aminophenoxy)phenyl]propane, 2,2-bis[3-methyl-4-(4-aminophenoxy)phenyl]propane, 2,2- Bis[4_(4-aminophenoxy)phenyl]butane, 2,2-bis[3-methyl-4-(4-aminophenoxy)phenyl]butane, 2,2- Bis[3,5-dimethyl-4-(4-aminophenoxy)phenyl]butane, 2,2-bis[3,5-dibromo-4-(4-aminophenoxy) Phenyl]butane, 1,1,1,3,3,3-hexafluoro-2,2-bis[3-methyl-4-(4-aminophenoxy)phenyl]propane, 1 , 1_double μ-Η-aminophenoxy)phenyl]cyclohexane, 1, 1-bis[4-(4-aminophenoxy)phenyl]cyclopentane, bis[4-( 4-aminophenoxy)phenyl], bis[4-(4-aminophenoxy)phenyl]ether, bis[4-(3-aminophenoxy)phenyl], 4 And 4'-carbonylbis(P-phenylene)diphenylamine, 4,4'-bis(4-aminophenoxy)biphenyl, etc., which may be used singly or in combination. Among them, 2,2-bis[(4-aminophenoxy)phenyl]propene is preferred. This paper scale applies to Chinese National Standard (CNS) A4 specification (210X 297 mm) -19- 1253457 A7 B7 V. Description of invention (1 is in addition to the above (el) aromatic diamine (e2) such as 1,3- Bis(3-aminophenoxy)benzene, 1,3-bis(4-aminophenoxy)benzene, 1,4-bis(4-aminophenoxy)benzene, 4,4'-[ 1,3-phenylphenylbis(1-methylethylidene)]diphenylamine, 4,4,-[1,4-phenylphenylbis(1-methylethylidene)]diphenylamine, 3, 3,-[1,3-phenylenebis(1-methylethylidene)]diphenylamine, 4,4,-diaminophenyl ether, 4,4·-diaminodiphenylmethane, 4,4,diamino-3,3,5,5|_tetramethyldiphenyl ether, 4,4,diamino-3,3,5,5,4-tetramethyldiphenyl Methane, 4,4'-diamino-3,3',5,5'-tetraethyldiphenyl ether, 2,2-[4,4'-diamino-3,3,,5, 5'-tetramethyldiphenyl]propane, m-phenylenediamine, p-phenylenediamine, 3,3·-diaminodiphenyl milling, hydrazine-xylylenediamine, toluenediamine, p-xylene Diamines, etc., can be used alone or in combination. In addition to the above (el) and (e2) , that is, an aliphatic or alicyclic diamine (e3) such as piperazine, hexamethylenediamine, heptamethylamine, tetramethylammonium, 3-methylthenemethyldiamine, etc. Further, when the thermoplastic resin (B2) is synthesized, the acid component which reacts with the diamine having the above-mentioned diamine polysiloxane as an essential component may be used for the above synthetic resin (B 1 ). The acid component (S). The amount of the acid component (S) formed by the aromatic dicarboxylic acid, the aromatic tricarboxylic acid, the aromatic tetracarboxylic acid or a reactive derivative thereof is the molecular weight of the obtained polymer. From the viewpoints of mechanical strength, heat resistance and the like, the total amount of the diamine is preferably 100 mol%, and the total amount is 80 to 120 mol%, particularly preferably 95 to 105 mol%. In the composition K, conductivity The mixing ratio of the powder C AD and the thermoplastic resin (B 1 ) is not limited. However, from the viewpoint of the conductivity of the formed coating film, etc., the component (B1) of the component (A1) is preferably 2 to 1 part by weight. 25 parts by weight, this paper size applies to Chinese National Standard (CNS) Α4 specifications (210Χ 297 mm) —.---.---^---- (Please read the notes on the back first) Fill in this page), 1Τ Ministry of Economic Affairs Intellectual Property Bureau Staff Consumer Cooperative Printed -20- 1253457 A7 __B7_ V. Invention Description (1 bow is preferably 4 to 14 parts by weight. Composition (Μ), conductive powder (A1 The mixing ratio with the thermoplastic resin ((2) is not limited, but it is preferably 2 to 25 parts by weight based on 100 parts by weight of the (Α2) component, from the viewpoint of coating film strength, toughness, and electrical conductivity. It is preferably 4 to 14 parts by weight. In the composition, the mixing ratio of the conductive powder (Α2) and the thermoplastic resin (Β2) is not limited, but the (Β2) component of the (Α2) component is 100 parts by weight in terms of flexibility, conductivity, and the like of the coating film. It is preferably 2 to 25 parts by weight, more preferably 4 to 14 parts by weight. The organic solvent (C) used for the composition Κ, L, Μ, Ν, for example, an aromatic solvent such as benzene, toluene or xylene; ketone such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone Solvent; diethyl ether, isopropyl ether, tetrahydrofuran, dioxane, ethylene glycol dimethyl ether, ethylene glycol diethyl ether, diethylene glycol dimethyl ether, diethylene glycol diethyl Ether solvent such as ethyl ether; ethyl acetate-η-propyl ester, isopropyl acetate, η-butyl acetate, ethylene glycol monomethyl ether acetate, ethylene glycol monoethyl ether acetate , ethylene glycol monobutyl ether acetate, diethylene glycol monomethyl ether acetate, diethylene glycol monomethyl ether acetate, propylene glycol monomethyl ether acetate, propylene glycol monomethyl ether An ester solvent such as acetate, propylene glycol monoethyl ether acetate or r-butyrolactone; a guanamine solvent such as dimethylformamide, dimethylacetamide or N-methylpyrrolidone. The solvent is used as a resin to dissolve the resin or to adjust the viscosity of the paste, and may be used singly or in combination of two or more. The amount of the organic solvent (C) added is based on the solubility of the resin, the viscosity of the paste, the dispersibility of the conductive powder, and the film formation property. For the thermoplastic resin (please read the back of the back sheet and fill out this page). Ordered by the Ministry of Economic Affairs, Intellectual Property Bureau, Staff and Consumer Cooperatives, printed on this paper scale, applicable to China National Standard (CNS) A4 specification (210X297 mm) -21 - 1253457 A7 B7 V. Invention description (1 bow iOO weight is generally 75 to 46 〇 0 parts by weight, preferably I25 to 3 〇 60 parts by weight. (Please read the following notes on the back side and fill out this page.) For the components containing the above-mentioned additives, for example, a lycra machine, a 3-seater roller machine, a ball mill, or the like can be used. A dispersing machine or the like is obtained by kneading and dispersing the respective components. Further, in order to improve the dispersibility and coatability of the conductive powder (dipping material), a dispersing agent or a coupling agent may be added. The dispersing agent used is preferably, for example, a carbon number of 16. a saturated fatty acid such as palmitic acid or stearic acid of 20; an unsaturated fatty acid such as oleic acid or linoleic acid having a carbon number of 16 to 18; and a metal salt such as sodium, potassium, calcium, zinc or copper of the saturated/unsaturated fatty acid; 1 or more. The amount of the agent added is preferably from 0.2 to 240 parts by weight, more preferably from 2 to 120, per 100 parts by weight of the resin, from the viewpoints of the dispersibility of the conductive powder, the conductivity of the coating film, and the adhesion between the coating film and the substrate. The Ministry of Economic Affairs, Intellectual Property Office, Staff Consumer Cooperative, printing coupling agents such as vinyl methoxy decane, vinyl triethoxy decane, vinyl tris (/3 - methoxy ethoxy) decane, / 3 -(3,4-epoxycyclohexyl)ethyltrimethoxydecane, r-glycidoxypropyltrimethoxydecane, r-glycidoxypropyltrimethoxydecane, r-ring Oxypropoxypropylmethyldiethoxydecane, N-/3-(aminoethyl)-r-aminopropylmethyldimethoxydecane, r-aminopropyltriethoxy a decane coupling agent such as decane, N-phenylaminopropyl.trimethoxydecane or r-mercaptopropyltrimethoxydecane, or a titanate coupling agent, an aluminate coupling agent, yttrium aluminate A coupling agent or the like is preferably added in an amount of not less than 3 parts by weight based on 1 part by weight of the thermoplastic resin. The composition of the present invention is suitable for a conductor layer of various electronic parts. For example, conductive circuit or electrode material. This paper scale applies to Chinese National Standard (CNS) A4 specification (210X29? mm) -22- 1253457 A7 B7 V. Invention description (2() (Please read the note on the back and fill in The electronic component of the present invention has a conductor layer formed by using the composition of the present invention. Various electronic components such as an aluminum electrolytic capacitor, a giant solid electrolytic capacitor, a ceramic capacitor, etc. using the composition as an electrode material; The plate is printed with various substrates which form a conductive circuit from the composition of the present invention; a conductive circuit formed by the composition of the present invention is used as a 1C card or the like for an antenna circuit. The composition of the present invention is also applicable to a cathode material of a solid electrolytic capacitor in which a valve acts as a metal. Preferably, the electronic component of the present invention is a solid electrolytic capacitor comprising a dielectric layer formed of a valve metal and a cathode layer comprising a dielectric oxide film, a solid electrolyte layer, and a conductor layer formed using the composition of the present invention. The solid electrolytic capacitor 10 of the example shown in FIG. 1 is printed by the Intellectual Property Office of the Intellectual Property Office of the Ministry of Economic Affairs, and includes an anode substrate 2 in which the anode wire 1 is buried, and a dielectric oxygen film (anodized film) sequentially formed on the anode substrate 2. 3) and a solid electrolyte layer (semiconductor layer) 4, and a capacitor element of the cathode 5 composed of the carbon layer 51 and the conductor layer 52. The valve action metal used in the anode substrate 2 is preferably molybdenum, aluminum, titanium, tantalum or the like. The shape of the anode base 2 is preferably a foil shape, a plate shape or a rod shape. The anode base 2 is formed by a method in which the valve metal powder is compression-molded in the form of an anode wire 1 in which a ruthenium wire or the like is embedded, and then heated at 2000 ° C for 10 minutes in a vacuum to obtain a sintered body. Then, a voltage is applied to the obtained sintered body (anode base 2) in a chemical solution such as nitric acid or phosphoric acid, and a dielectric oxide film 3 such as Ta2?3 is formed on the surface of the anode base 2 after the formation. The oxide film is preferably a layer formed by an oxide of the anode base metal itself, but may be a dielectric oxygen sheet different from the anode substrate. The Chinese National Standard (CNS) A4 specification (210×297 mm) ~ ' 1253457 A7 B7 V. INSTRUCTIONS (21) (Please read the notes on the back and fill out this page). After the dielectric oxide film is formed, the sintered body is immersed in a semiconductor mother liquid such as a manganese nitrate solution, and after being impregnated with a liquid, it is thermally decomposed by 2 〇〇 to 3 5 〇 π and formed into a sintered body (sinter surface) to be oxidized. A solid electrolyte layer 4 mainly composed of a manganese layer. After the thermal decomposition, it is reformed to repair the dielectric oxide film 3 at the time of sintering, and if necessary, repeat the immersion, firing and reforming steps of 5 to 10 times or more to form the solid electrolyte layer 4 having a desired thickness. Further, as the solid electrolyte layer, a TCNQ (7,7,8,-tetracyano D-quinoline dimethyl hydrazine) complex called an organic semiconductor or a polypyrrole, a polythiophene or a polyaniline of a conductive polymer can be used. Formed. After the solid electrolyte layer 4 is formed, a carbon paste is applied, and after drying, a cathode layer 5 - a portion of the carbon layer 5 1 is formed, and then a conductor layer (silver layer or silver paste layer) of another portion of the cathode layer is formed thereon by using the composition of the present invention. 5 2. The lead frame 7 for taking out the cathode is connected to the obtained conductive layer 52' by soldering or a conductive adhesive 6 or the like, and the anode lead drawn from the sintered body 2 is welded to the lead frame 7 or the like. Finally, it is sealed by an external resin by a resin dipping method, a resin molding method, or the like. The obtained solid electrolytic capacitor is generally 2 to 7111111, 苋 1.25 to 4.3 mm, and 1.2 to 2.8 mm. Printed by the Intellectual Property Office of the Ministry of Economic Affairs, the Consumers' Cooperatives. The present invention will now be described in more detail by way of examples. Further, the measurement methods and evaluation methods of the various characteristics in the examples are as follows. [Aspect ratio] 2 g of a main component (N 〇.丄〇_ 8130) 8 g of a low-viscosity epoxy resin (manufactured by Kura Co., Ltd.) and a curing agent (ν〇·10-8132) were mixed, and 2 g of the powder for measurement was added. 'When fully dispersed, defoaming at 30 ° C vacuum, 3 (standing at TC for 1 〇 hours to make the paper size applicable to China National Standard (CNS) A4 specification (210X 297 mm) -24-1253457 A7 B7 V. DESCRIPTION OF THE INVENTION (2 bow precipitation, resin hardening. Thereafter, the obtained cured product is cut in the vertical direction.) The cross section is observed 1000 times with a microscope, and the long diameter/short diameter of 150 particles appearing in the cross section is obtained, and then averaged.値 is the aspect ratio. [Average particle size] The average particle size of the powder is measured by a Masdar granulator (manufactured by Maruman Co., Ltd.) [Copper exposure area] Five silver-plated copper powder particles are randomly taken out. Observed by a scanning-type Auger electron spectroscopic analyzer, and quantitative analysis of precious metal (silver) and non-precious metal (copper) by Auger image, after calculating the copper occupancy rate, the average enthalpy of five measurements was used as the copper exposed area ( %). [paste viscosity] The temperature in the constant temperature layer is set to 25 °C, using the east The E-type viscometer of the meter is measured by 3° cone, and the viscosity of the paste is measured after the start of measurement to 1 minute (please read the note on the back and fill in the page) -------m --. ....I------ n :―I·- -装·

、1T 經濟部智慧財產局員工消費合作社印製 [膏粘度之經時變化] 將所得膏放置於30°C恒溫槽內6個月後,測定其粘度。 [體積電阻率] 利用雙橋式電阻測定器(橫河電氣公司製TYPE2769 ) 測定使用膏而得之乾燥塗膜之體積電阻率。 本紙張尺度適用中國國家標準(CNS ) Α4規格(210X 297公釐) -25- 1253457 A7 B7 經濟部智慧財產局員工消費合作社印製 五、發明説明(2弓 [遷移特性] 使用體積電阻率測定用之乾燥塗膜,於乾燥塗膜中央 形成間隔2mm電極後,?問下純水以覆蓋全部電極,再對兩端 施加7V電壓,以所測得之銀移動至電極間短路爲止之時間 評估遷移特性。 [邊緣包裹性] 將lmmx lmmx 1.5mm立方體狀之鉅燒結體浸漬於測定 用膏中,乾燥後,以透明環氧樹脂外裝所得元件,室溫下 放置10小時使其硬化。其後利用鑽石切割機切斷立方體長 邊中央部,以砂紙及硏磨粒子硏磨後,作爲評估用元件。 以電子顯微鏡觀察評估用元件4個角之膏包裹狀態。評估A : 良好,邊緣部之塗膜厚爲1 // m以下,C:邊緣部有缺損 部分。 [塗膜強度] 利用塗布機,以1 80 °C乾燥1小時後,於特氟隆板上形 成膜厚5 0 // m之銀膜。由特氟隆板剝取薄膜,製作寬5mmX 40mm短冊狀之試驗片。 其後利用拉伸強度試驗機(今田製作所製:拉伸壓縮 試驗器SL-200 1 ),測定塗膜強度。 [塗膜之撓性] (請先閱讀背面之注意事項再填寫本頁) 裝·1T Ministry of Economic Affairs Intellectual Property Bureau employee consumption cooperative printing [Change in viscosity of paste] The viscosity of the obtained paste was placed in a thermostat at 30 ° C for 6 months. [Volume Resistivity] The volume resistivity of the dried coating film obtained by using the paste was measured by a double bridge resistance measuring instrument (Model 2769 manufactured by Yokogawa Electric Co., Ltd.). This paper scale applies to China National Standard (CNS) Α4 specification (210X 297 mm) -25- 1253457 A7 B7 Ministry of Economic Affairs Intellectual Property Bureau employee consumption cooperative printing 5, invention description (2 bow [migration characteristics] using volume resistivity determination After drying the coating film, after forming a 2 mm-interval electrode in the center of the dried coating film, pure water was applied to cover all the electrodes, and then 7 V was applied to both ends to evaluate the time until the measured silver moved to the short circuit between the electrodes. [Missing property] The lmmx lmmx 1.5mm cube-shaped giant sintered body was immersed in the measurement paste, and after drying, the obtained element was externally sealed with a transparent epoxy resin, and allowed to stand at room temperature for 10 hours to be hardened. After that, the center of the long side of the cube was cut by a diamond cutter, and it was honed by sandpaper and honing particles, and used as an evaluation component. The state of the paste of the four corners of the evaluation component was observed by an electron microscope. Evaluation A: Good, edge portion The coating film thickness is 1 // m or less, and C: there is a defect portion at the edge portion. [Coating film strength] After drying at 1 80 ° C for 1 hour by a coater, a film thickness of 5 0 / is formed on the Teflon plate. / m Silver film. The film was peeled off from a Teflon plate to prepare a test piece having a width of 5 mm X 40 mm. Then, a tensile tester (manufactured by Imada, Ltd.: tensile compression tester SL-200 1 ) was used to measure the film. Strength [Flexibility of coating film] (Please read the notes on the back and fill in this page)

、1T 本紙張尺度適用中國國家標準(CNS ) Α4規格(210Χ297公釐) -26 - 1253457 A7 B7 五、發明説明( (請先閱讀背面之注意事項再填寫本頁) 將膏以寬2毫方式塗布於厚125//m、寬lcm、長10cm之 PET薄膜上,以180°C乾燥1小時,重覆進行膜一端接觸表面 的另一端後,再接觸背面的另一端,以測定幾次後塗膜出 現龜裂。 [電容器特性] 依據JIS C 5 102- 1994 (電子機器用固定電容器之試驗方 法),測定鉅電容器之特性。又,利用LCR計器測定等價直 列電阻(ESR )。漏電流(LC )爲,製作導電體層使用測 定用膏之鉅電容器後,利用數據微少電流計(阿德曼測試; R8340A )測定85°C,85% RH環境下放置lOOOhr及2000hr之値 。tan5、阻抗係利用休雷頓公司製LCR計器(4284A)測定 。Cap (靜電容量)係利用LCR (休雷頓製4284A )測定。 [電容器之過電壓負荷特性] 對鉅電容器之定格電壓施加過電壓後,測定電容器特 性,以確認電容器之破壞數。 經濟部智慧財產局員工消費合作社印製 [焊接接著性] 將寬lcm、長2cm、厚0.5mm之鋁板浸漬lcm測定用膏後 取出,以烘烤乾燥機於1 80 °C下乾燥1小時’以作爲評估用 試料。將評估用試料浸漬於助熔劑後,再浸漬於各設定溫 度之焊接浴,以觀察焊接之接著狀態。評估A:焊接塗布面 積80%以上之物,B : 50%以上低於80%之物’ C: 30%以上低 -27- 本紙張尺度適用中國國家標準(CNS ) A4規格(210X 297公釐) 1253457 A7 B7 五、發明説明(2今 於50%之物,D:低於30%之物。 [焊接接著性試驗條件] 焊接溫度 230 °C、260°C、290〇C 3 2 0 °C 浸漬時間 2秒 使用焊接浴(Sn:Pb) 6:4 9:1 使用助熔劑 松脂 JIS K5902 1級 1 號 30vol°/〇 溶劑異丙基醇 7Gvg1% (請先閲讀背面之注意事項再填寫本頁) •裝· [電容器之焊接耐熱性] 測定鉅電容器浸漬於焊接浴10秒後之容量變化率。焊 接浴溫度:23CTC、26(TC、29CTC。 [電容器之耐熱衝撃性] 將钽電容器投入熱衝撃試驗器中,循環1 000次後取出 測定電容器特性。熱衝撃條件爲,-5(TC至80°C下進行。即 ,-50°C之槽中放置30分鐘後,3分鐘以內移入80°C之槽中放 置30分鐘,再於3分鐘內移入-50°C之槽中,視爲1次循環。 〈熱塑性樹脂(B1)之合成例1&gt; 氮氣下,將二胺用BAPP ( 2,2-雙[4-(4-胺基苯氧基)苯 基]丙烷)100g ( 0.24莫耳)溶解於備有溫度計、攪拌機、 氮導入管及冷卻管之1升四口燒瓶中的N_甲基-2-吡略烷酮 ^紙張尺度適用中國國家標準(CNS ) A4規格(21〇X29&lt;7公釐) ~~ 訂 經濟部智慧財產局員工消費合作社印製 1253457 經濟部智慧財產局員工消費合作社印製 A7 ____ B7五、發明説明(θ 4 0 0 g中。將所得溶液冷卻至-1 〇 °c後,於溶液溫度不超過_ 5 t下,加入間苯二酸二氯化物49.5g ( 0.24莫耳),再加入 環氧丙烷56.6g。室溫下攪拌3小時後,將反應液投入純水中 使聚合物單離,乾燥後再溶解於N-甲基-2-吡咯烷酮,其後 將所得溶液投入純水中,以精製聚醯胺聚合物。 &lt;熱塑性樹脂(B1)之合成例2&gt; ®熱下’將—^女用2’ 2 -雙[4-(4 -胺基苯氧基)苯基]丙院 )205g ( 500毫莫耳)溶解於備有溫度計、攪拌機、氮導入 管及冷卻管之3升四口中的二乙二醇二甲基醚η 17 7g。將所 得溶液冷卻至-1 0 °C後,於溶液溫度不超過_ 5 °C下,加入偏 苯三酸酐單氯化物105.3g,再加入環氧丙烷87g。室溫下攪 拌3小時後,使反應液粘度上升而成透明液後,追加二乙二 醇二甲基醚841g,再攪拌1小時。其後加入乙酸酐I28g及吡 啶64g,於60 °C持續攪拌一晝夜。將所得反應液投入甲醇 250g中,使聚醯胺醢亞胺單離,乾燥後再溶解於n,N-二甲 基甲醯胺,其後投入甲醇中,得聚醯胺醯亞胺聚合物之生 成物。 &lt;熱塑性樹脂(B2)之合成例1&gt; 氮氣下,將二胺用2,2-雙[4-(4-胺基苯氧基)苯基]丙烷 6 5.6g ( 160毫莫耳)及一般式(V)所示二胺基矽氧烷(信 越化學工業(股)製,X-22-161B; —般式(V)中m = 38、Y、 -C3H6-、Y、-CH3 ) 64g ( 40毫莫耳)(莫耳比爲 80莫耳 %/ 20 (請先閲讀背面之注意事項再填寫本頁) 本紙張尺度適用中國國家標準(CNS ) A4規格(21〇X297公釐) 29- 1253457 Α7 Β7 五、發明説明(27) 莫耳)溶解於備有溫度計、攪拌機、氮導入管及冷卻管之 四口燒瓶中的二乙二醇二甲基醚3 3 5g中。 (請先閱讀背面之注意事項再填寫本頁) 將所得溶液冷卻至-10°C後,於溶液溫度不超過_5t: γ ,加入間苯二酸二氯化物40.6g ( 200毫莫耳),再加入環氧 丙烷23.2g,其後追加二乙二醇二甲基醚96g,室溫下攪枠3 小時後,將反應液投入甲醇中使聚合物單離,乾燥後再溶 解於二甲基甲醯胺中,接著投入甲醇中,以精製聚醯胺聚 矽氧烷共聚物。 &lt;熱塑性樹脂(B2)之合成例2&gt; 氮氣下,將二胺用2, 2-雙[4-(4-胺基苯氧基)苯基]丙院 174.3g ( 425毫莫耳)及二胺基丙基四甲基二矽氧烷18.6§ ( 信越化學工業(股)製,LP7 1 00) ( 75毫莫耳)(莫耳比爲85莫 耳%/ 15莫耳)溶解於備有溫度計、攪拌機、氮導入管及冷 卻管之四口燒瓶中的二乙二醇二甲基醚1177g中。 經濟部智慧財產局員工消費合作社印製 將所得溶液冷卻至-1 0 °C後,於溶液溫度不超過-5 °C下 ,加入偏苯三酸酐單氯化物105.3g( 500毫莫耳),再加入 環氧丙烷87g。室溫下攪拌3小時,使反應液粘度上升而成 爲透明液後,再追加二乙二醇二甲基醚84 1 g。攪拌1小時後 加入乙酸酐128g及吡啶64g,再於6(TC下攪拌一晝夜。將所 得反應液投入η-己烷/甲醇=1/1 (重量比)之大量混合溶劑 中,使聚合物單離,乾燥後,再溶解於Ν,Ν-二甲基甲醯胺 ’其後投入甲醇中,以精製聚醯胺醯亞胺聚矽氧烷共聚物 ,再減壓乾燥。 本紙張尺度適用中國國家標準(CNS ) Α4規格(210X297公釐) -30- 1253457 A7 B7 經濟部智慧財產局員工消費合作社印製 五、發明説明(2芍 &lt;鍍銀銅粉(al)之製作例&gt; 以稀鹽酸及純水洗淨利用噴霧法製得之平均粒徑5.1 从m的球狀銅粉(日本噴霧加工(股)製,商品名SFR_Cu )後 ’以水每1升含AgCN 80g及NaCN 75g之鍍銀液,對球狀銅粉 以銀量爲1 5重量%方式進行取代,再水洗、乾燥,得鍍銀銅 粉。 將所得鍍銀銅粉7 5 0g及直徑5mm之氧化銷球3kg放入2升 球磨機容器內,回轉40分鐘後,得長寬比平均爲1.3及長徑 平均粒徑爲5.5// m之鍍銀銅粉。 &lt;鍍銀銅粉(a2)之製作例&gt; 以稀鹽酸及純水洗淨利用噴霧法製得之平均粒徑5.1 // m的球狀銅粉(日本噴霧加工(股)製,商品名SFR_Cu )後 ,以水每1升含有AgCN 80g及NaCN 75g之鑛銀溶液,對球狀 銅粉以銀量爲20重量%方式進行取代,再水洗、乾燥,得鍍 銀銅粉。 將所得鍍銀銅粉750g及直徑5mm之氧化锆球3kg投入2升 球磨機容器內,回轉40分鐘後,得平均粒徑8.1 // m之鍍銀 銅粉。 實施方式 實施例K 1 依表1所示比率,將上述鍍銀銅粉(a 1 )之製作例所得 (請先閱讀背面之注意事項再填寫本頁) -裝- 訂, 1T This paper scale applies to China National Standard (CNS) Α 4 specifications (210Χ297 mm) -26 - 1253457 A7 B7 V. Invention Description ((Please read the back note first and then fill in this page) Put the paste in 2 Width Applying on a PET film having a thickness of 125/m, a width of 1 cm, and a length of 10 cm, drying at 180 ° C for 1 hour, repeating the other end of the contact surface of one end of the film, and then contacting the other end of the back surface to measure a few times. Cracking of the coating film [Capacitor characteristics] The characteristics of the giant capacitor were measured in accordance with JIS C 5 102-1994 (Test method for fixed capacitors for electronic equipment). The equivalent in-line resistance (ESR) was measured by an LCR meter. (LC): After making a giant capacitor using a measuring paste for a conductor layer, it was measured at 85 ° C using a data micro-amperometer (Ademan test; R8340A), and placed at 1000 ° C for an interval of 1000 hr and 2000 hr. It is measured by an LCR meter (4284A) manufactured by Haleton Co., Ltd. Cap (electrostatic capacity) is measured by LCR (Hybridon 4284A). [Overvoltage load characteristics of capacitor] After applying an overvoltage to the constant voltage of a giant capacitor, Capacitor characteristics were measured to confirm the number of damages of the capacitor. Printed by the Ministry of Economic Affairs, Intellectual Property Office, and the Consumer Cooperatives [welding adhesiveness] The aluminum plate with a width of lcm, a length of 2 cm, and a thickness of 0.5 mm was immersed in a lcm measuring paste and then taken out for baking. The machine was dried at 1 80 ° C for 1 hour to be used as an evaluation sample. The evaluation sample was immersed in a flux and then immersed in a solder bath at each set temperature to observe the subsequent state of the solder. Evaluation A: Solder coating area More than 80%, B: 50% or more and less than 80% 'C: 30% or more and low-27- This paper scale applies to China National Standard (CNS) A4 specification (210X 297 mm) 1253457 A7 B7 V. DESCRIPTION OF THE INVENTION (2 present in 50%, D: less than 30%. [Welding adhesion test conditions] Welding temperature 230 ° C, 260 ° C, 290 ° C 3 2 0 ° C immersion time 2 seconds use Solder bath (Sn:Pb) 6:4 9:1 Use flux rosin JIS K5902 Level 1 No. 1 30vol ° / 〇 solvent isopropyl alcohol 7Gvg1% (Please read the back of the note before you fill out this page) • Install · [Solder heat resistance of capacitor] After measuring the giant capacitor immersed in the solder bath for 10 seconds Capacity change rate: solder bath temperature: 23 CTC, 26 (TC, 29 CTC. [Heat-resistant heat-resistance of capacitor] The tantalum capacitor was placed in a hot-dip tester, and the characteristics of the capacitor were taken out after 1 000 cycles. The hot-pressing condition was -5 (TC to 80 ° C. Namely, after standing in a tank at -50 ° C for 30 minutes, it was placed in a tank of 80 ° C for 3 minutes within 3 minutes, and then transferred into a tank of -50 ° C in 3 minutes, which was regarded as 1 cycle. <Synthesis Example 1 of Thermoplastic Resin (B1)&gt; The diamine was dissolved in BAPP (2,2-bis[4-(4-aminophenoxy)phenyl]propane) 100 g (0.24 mol) under nitrogen. N-methyl-2-pyrrolidone in a 1 liter four-necked flask equipped with a thermometer, a stirrer, a nitrogen inlet tube and a cooling tube. The paper size is applicable to the Chinese National Standard (CNS) A4 specification (21〇X29&lt;7厘) ~~ The Ministry of Economic Affairs Intellectual Property Bureau employees consumption cooperatives printed 1253457 Ministry of Economic Affairs Intellectual Property Bureau employees consumption cooperatives printed A7 ____ B7 five, invention description (θ 4 0 0 g. Cool the resulting solution to -1 〇 ° After c, 49.5 g (0.24 mol) of isophthalic acid dichloride was added at a solution temperature of not more than 5 t, and then 56.6 g of propylene oxide was added. After stirring at room temperature for 3 hours, the reaction liquid was poured into pure. The polymer is separated in water, dried and then dissolved in N-methyl-2-pyrrolidone, and then the resulting solution is poured into pure water to purify the polyamine polymer. <Chemical Resin (B1) Synthesis Example 2&gt;®Hot under 'will-^ female 2' 2 -bis[4-(4-aminophenoxy)phenyl]propyl) 205g (500 millimolar) In equipped with a thermometer, a stirrer, a nitrogen inlet tube and a cooling tube within three-liter four-mouth diethylene glycol dimethyl ether η 17 7g. After the resulting solution was cooled to -10 ° C, 105.3 g of trimellitic anhydride monochloride was added at a solution temperature not exceeding _ 5 ° C, and then 87 g of propylene oxide was added. After stirring at room temperature for 3 hours, the viscosity of the reaction liquid was raised to obtain a transparent liquid, and then 841 g of diethyl dimethyl ether dimethyl ether was added thereto, followed by stirring for 1 hour. Thereafter, acetic anhydride I28 g and pyridine pyridine 64 g were added, and stirring was continued at 60 ° C for a day and night. The obtained reaction liquid was poured into 250 g of methanol to separate the polyamidoximine, and after drying, it was dissolved in n,N-dimethylformamide, and then it was put into methanol to obtain a polyamidoximine polymer. The product. &lt;Synthesis Example 1 of Thermoplastic Resin (B2)&gt; Under a nitrogen gas, 2,2-bis[4-(4-aminophenoxy)phenyl]propane 6 5.6 g (160 mmol) was used for the diamine. The general formula (V) shows a diamine oxirane (manufactured by Shin-Etsu Chemical Co., Ltd., X-22-161B; - (v), m = 38, Y, -C3H6-, Y, -CH3) 64g (40 millimoles) (Morby is 80% by mole / 20 (please read the back note first and then fill out this page) This paper size applies to the Chinese National Standard (CNS) A4 specification (21〇X297 mm) 29- 1253457 Α7 Β7 5. Inventive Note (27) Mohr was dissolved in 3,5 g of diethylene glycol dimethyl ether in a four-necked flask equipped with a thermometer, a stirrer, a nitrogen introduction tube, and a cooling tube. (Please read the precautions on the back and fill out this page.) After cooling the solution to -10 ° C, do not exceed _5t: γ at the solution temperature and add 40.6g (200 millimoles) of isophthalic acid dichloride. Further, 23.2 g of propylene oxide was added, and then 96 g of diethylene glycol dimethyl ether was added thereto, and the mixture was stirred at room temperature for 3 hours, and then the reaction liquid was poured into methanol to separate the polymer, and then dissolved in dimethyl after drying. The carbamide is then added to methanol to refine the polyamine polyoxyalkylene copolymer. &lt;Synthesis Example 2 of Thermoplastic Resin (B2)&gt; 174.3 g (425 mmol) of 2,2-bis[4-(4-aminophenoxy)phenyl]propene was used as the diamine under nitrogen. Diaminopropyltetramethyldioxane 18.6§ (manufactured by Shin-Etsu Chemical Co., Ltd., LP7 1 00) (75 millimoles) (85 molars per mole ratio / 15 moles) dissolved in preparation There were 1177 g of diethylene glycol dimethyl ether in a four-necked flask of a thermometer, a stirrer, a nitrogen introduction tube, and a cooling tube. Printing by the Intellectual Property Office of the Ministry of Economic Affairs, the Consumer Cooperatives, after cooling the obtained solution to -10 °C, adding 105.3 g (500 mmol) of trimellitic anhydride monochloride at a solution temperature not exceeding -5 °C, and then adding the ring. Oxypropane 87g. After stirring at room temperature for 3 hours, the viscosity of the reaction liquid was increased to form a transparent liquid, and then 84 g of diethylene glycol dimethyl ether was added. After stirring for 1 hour, 128 g of acetic anhydride and 64 g of pyridine were added, and the mixture was stirred at 6 (TC) for a day and night. The obtained reaction liquid was poured into a large amount of a mixed solvent of η-hexane/methanol = 1/1 (weight ratio) to obtain a polymer. After separation, after drying, it is redissolved in hydrazine and hydrazine-dimethylformamide, which is then added to methanol to refine the polyamidoamine polyoxyalkylene copolymer and then dried under reduced pressure. China National Standard (CNS) Α4 Specifications (210X297 mm) -30- 1253457 A7 B7 Ministry of Economic Affairs Intellectual Property Bureau Employees Consumption Cooperative Printed 5, Invention Description (2芍&lt;Prepared Example of Silver-plated Copper Powder (al)&gt; Washed with dilute hydrochloric acid and pure water, the spherical copper powder with an average particle diameter of 5.1 from m (manufactured by Nippon Spray Processing Co., Ltd., trade name SFR_Cu) contains 80 g of AgCN and 75 g of NaCN per 1 liter of water. The silver plating liquid is substituted for the spherical copper powder by a silver content of 15% by weight, and then washed with water and dried to obtain a silver-plated copper powder. The obtained silver-plated copper powder is 7550 g and the oxidation pin ball having a diameter of 5 mm is 3 kg. Put into a 2 liter ball mill container, after 40 minutes of rotation, the average aspect ratio is 1.3 and the long diameter average Silver-plated copper powder with a diameter of 5.5//m. &lt;Preparation of silver-plated copper powder (a2)&gt; Spherical copper with an average particle diameter of 5.1 // m obtained by spraying with dilute hydrochloric acid and pure water After the powder (manufactured by Nippon Spray Processing Co., Ltd., trade name: SFR_Cu), the spherical copper powder is replaced with 20% by weight of silver in an amount of 20% by weight of AgCN, and the amount of silver is 20% by weight per 1 liter of water. The silver-plated copper powder was obtained by adding 750 g of the obtained silver-plated copper powder and 3 kg of zirconia balls having a diameter of 5 mm into a 2-liter ball mill vessel, and after 40 minutes of rotation, a silver-plated copper powder having an average particle diameter of 8.1 // m was obtained. EMBODIMENT EXAMPLE K 1 According to the production example of the above-mentioned silver-plated copper powder (a 1 ) according to the ratio shown in Table 1 (please read the note on the back side and then fill in the page) - Pack - Order

本纸張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 1253457 A7 B7 五、發明説明(巧 (請先閲讀背面之注意事項再填寫本頁) 的鍍銀銅粉及銀粉(得庫撒公司製 SF # 7 鱗片狀 zp 均粒徑6.8 // m )加入上述熱塑性樹脂(B 1 )之合成例所得 的聚醯胺聚合物22.2重量份中加入二乙二醇二甲基醚222.2 重量份溶解而得的淸漆中,利用分散機分散2〇分鐘後,得 組成物(膏)K。將所得膏脫泡後,利用網版印刷法將一定 量塗布於玻璃載片上(塗布面積:lcmx 7.5cm,塗布厚:40 ± 1 0 // m ),再利用間歇式乾燥爐以1 8 0 °C乾燥1小時,得乾 燥塗膜。測定所得乾燥塗膜之體積電阻率及遷移特性。使 用所得之膏製作鉅電容器,再測定等價直列電阻及漏電流 ,及評估邊緣包裹性。 實施例K2 除了噴霧法所製得之球狀銅粉的平均粒徑爲5.9 // m, 鍍銀銅粉之長寬比爲1 . 5及平均粒徑爲6.7 // m外,其他同實 施例K 1。 實施例K3 經濟部智慧財產局員工消費合作社印製 除了噴霧法所製得之球狀銅粉的平均粒徑爲5.9 // m, 球磨機之回轉時間爲60分鐘,鍍銀銅粉之長寬比爲2.5及平 均粒徑爲8.0 // m外,其他同實施例K 1。 實施例K4 除了噴霧法所製得之球狀銅粉的平均粒徑爲4.2 // m, 球磨機之回轉時間爲1 20分鐘,鍍銀銅粉之長寬比爲1 2及平 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) -32- 1253457 A7 B7 五、發明説明(39 均粒徑爲7.2 // m外,其他同實施例Κ 1。 (請先閱讀背面之注意事項再填寫本頁) 實施例K5 除了噴霧法所製得之球狀銅粉的平均粒徑爲3 . 5 // m, 球磨機之回轉時間爲180分鐘,鍍銀銅粉之長寬比爲20及平 均粒徑爲6.2 // m外,其他同實施例K 1。 實施例K6 除了噴霧法所製得之球狀銅粉的平均粒徑爲0.1 // m, 鍍銀銅粉之長寬比爲3.2及平均粒徑爲0.2// m外,其他同實 施例K 1。 實施例K7 除了噴霧法所製得之球狀銅粉的平均粒徑爲〇. 6 // m, 鑛銀銅粉之長寬比爲3及平均粒徑爲1.0 // m外,其他同實施 例K 1。 實施例K8 經濟部智慧財產局員工消費合作社印製 除了噴霧法所製得之球狀銅粉的平均粒徑爲1 . 〇 # m ’ 鍍銀銅粉之長寬比爲3 . 1及平均粒徑爲1 . 5 // m外,其他同實 施例K 1。 實施例K9 除了噴霧法所製得之球狀銅粉的平均粒徑爲5 . 5 # m ’ -33- 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 1253457 A7 B7 經濟部智慧財產局員工消費合作社印製 五、發明説明(31) 鍍銀銅粉之長寬比爲3 . 1及平均粒徑爲8.0 // m外,其他同實 施例K 1。 實施例K 1 0 除了噴霧法所製得之球狀銅粉的平均粒徑爲8.2 // m, 鍍銀銅粉之長寬比爲3.2及平均粒徑爲1 2 // m外,其他同實 施例K 1。 實施例K 1 1 除了噴霧法所製得之球狀銅粉的平均粒徑爲1 3.6 // m, 鍍銀銅粉之長寬比爲3.0及平均粒徑爲2 0 // m外,其他同實 施例κ 1。 實施例κ 1 2 除了噴霧法所製得之球狀銅粉的平均粒徑爲4.6 // m, 對球狀銅粉之銀取代量爲0.5重量%,鍍銀銅粉之長寬比爲 3 . 5及平均粒徑爲6,7 # :^外,其他同實施例Κ 1。 實施例K13 除了噴霧法所製得之球狀銅粉的平均粒徑爲3.8 // m, 對球狀銅粉之銀取代量爲1.Q重量%,鍍銀銅粉之長寬比爲 3 . 1及平均粒徑爲5 . 3 v m外,其他同實施例κ 1。 實施例K14 (請先閱讀背面之注意事項再填寫本頁) 裝· 本紙張尺度適用中國國家標準(CNS ) M規格(2丨⑴97公羡 -34- 1253457 A7 B7 五、發明説明( (請先閲讀背面之注意事項再填寫本頁) 除了噴霧法所製得之球狀銅粉的平均粒徑爲3 6 # m, 對球狀銅粉之銀取代量爲1.5重量%,鍍銀銅粉之長寬比爲 3 . 5及平均粒徑爲5.2 // m外,其他同實施例κ 1。 實施例K 1 5 除了噴霧法所製得之球狀銅粉的平均粒徑爲4.3 # m, 對球狀銅粉之銀取代量爲25重量%,鍍銀銅粉之長寬比爲 3,4及平均粒徑爲6.2 //历外,其他同實施例κ 1。 實施例κ 1 6 除了噴霧法所製得之球狀銅粉的平均粒徑爲5 . 〇 # m, 對球狀銅粉之銀取代量爲3 5重量%,鍍銀銅粉之長寬比爲 3 . 8及平均粒徑爲7.5 // m外,其他同實施例K 1。 實施例Κ 1 7 經濟部智慧財產局員工消費合作社印製 除了噴霧法所製得之球狀銅粉的平均粒徑爲4.7 # m, 對球狀銅粉之銀取代量爲50重量%,鍍銀銅粉之長寬比爲 4.〇及平均粒徑爲7.1 v❿外,其他同實施例K1。 實施例Κ 1 8 除了噴霧法所製得之球狀銅粉的平均粒徑爲5.9 // m, 對球狀銅粉之銀取代量爲20重量%,鍍銀銅粉之長寬比爲 2.5及平均粒徑爲8.0# m,銀粉(德力化學TCG-1)之形狀 爲球狀及平均粒徑爲2.0 // m外,其他同實施例Κ 1。 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) -35- 1253457 A7 Γ--s —JL7_ 五、發明説明(3今 實施例κ 1 9 (請先閲讀背面之注意事項再填寫本頁) 除了噴霧法所製得之球狀銅粉的平均粒徑爲5.9 # m, 對球狀銅粉之銀取代量爲2〇重量%,鍍銀銅粉之長寬比爲 2 · 5及平均粒徑爲8 . 〇 β历外,其他同實施例κ 1。 實施例K20 除了噴霧法所製得之球狀銅粉的平均粒徑爲5.9 # m, 對球狀銅粉之銀取代量爲2〇重量%,鍍銀銅粉之長寬比爲 2.5及平均粒徑爲8 . 〇 #❿外,其他同實施例κ 1。 實施例K21 除了噴霧法所製得之球狀銅粉的平均粒徑爲5.9 // m, 對球狀銅粉之銀取代量爲20重量%,鑛銀銅粉之長寬比爲 2.5及平均粒徑爲8,0 // m外,其他同實施例K 1。 實施例K22 經濟部智慧財產局員工消費合作社印製 除了噴霧法所製得之球狀銅粉的平均粒徑爲5.9 // m, 對球狀銅粉之銀取代量爲2〇重量%,鍍銀銅粉之長寬比爲 2.5及平均粒徑爲8.〇//111外,其他同實施例5:1。 實施例K23 除了噴霧法所製得之球狀銅粉的平均粒徑爲5.9 // m, 對球狀銅粉之銀取代量爲20重量%,鍍銀銅粉之長寬比爲 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) -36- 1253457 A7 B7 五、發明説明( 2.5及平均粒徑爲8 . 〇 e m外,其他同實施例K 1。 實施例K24 (請先閱讀背面之注意事項再填寫本頁) 除了噴霧法所製得之球狀銅粉的平均粒徑爲5.9 # m, 對球狀銅粉之銀取代量爲20重量%,鍍銀銅粉之長寬比爲 2.5及平均粒徑爲8 . 〇 # ;^外,其他同實施例K 1。 實施例K25 除了使用上述熱塑性樹脂(B 1 )之合成例2所得的聚 醯胺醯亞胺聚合物,噴霧法所製得之球狀銅粉的平均粒徑 爲5.9 // m,對球狀銅粉之銀取代量爲1 5重量%,鍍銀銅粉之 長寬比爲2.5及平均粒徑爲8.0// m外,其他同實施例K1。 實施例K26 除了使用上述熱塑性樹脂(B 1 )之合成例2所得的聚 醯胺醯亞胺聚合物,噴霧法所製得之球狀銅粉的平均粒徑 爲4.4// m,對球狀銅粉之銀取代量爲15重量%,鍍銀銅粉之 長寬比爲3.2及平均粒徑爲6.5 // m外,其他同實施例K1 ° 經濟部智慧財產局員工消費合作社印製 比較例K 1 除了噴霧法所製得之球狀銅粉的平均粒徑爲13.8 # m ’ 對球狀銅粉之銀取代量爲1 5重量%,球磨機之回轉時間爲 240分鐘,鍍銀銅粉之長寬比爲25及平均粒徑爲26 #①外 其他同實施例K1。 本紙張尺度適用中國國家標準(CNS ) A4規格(210X 297公釐) _ 1253457 經濟部智慧財產局員工消費合作社印製 A7 ____ B7五、發明説明(3弓 比較例K2 除了使用上述熱塑性樹脂(B 1 )之合成例2所得的聚 醯胺醯亞胺聚合物,噴霧法所製得之球狀銅粉的平均粒徑 爲1 3.8 // m,對球狀銅粉之銀取代量爲1 5重量%,球磨機之 回轉時間爲240分鐘,鍍銀銅粉之長寬比爲25及平均粒徑爲 26// m外,其他同實施例K1。 比較例K3 除了以球狀銅粉(三井金屬鑛以MFP 11 10平均粒徑1.1 A m )取代鍍銀銅粉外,其他同實施例K1。 比較例K4 除了不含銀粉外,其他同實施例K 1。 比較例K5 除了不含鍍銀銅粉外,其他同實施例K1。 所得結果如表K1及表K2所示。 實施例1 將鍍銀銅粉(a2 )製作例所得之鍍銀銅粉(銅露出面 積20% ) 118.8重量份及銀粉(得庫撒公司製 SF # 7 鱗 片狀 平均粒徑6.8 // m ) 79.2重量份加入上述熱塑性樹脂 (B 1 )之合成例1所得的聚醯胺聚合物2 2.2重量份中加入二 (請先閱讀背面之注意事項再填寫本頁) ---- -—---I ! -- In 111- ; ---裝 訂This paper scale applies to China National Standard (CNS) A4 specification (210X297 mm) 1253457 A7 B7 V. Invention Description (Choose (please read the back note first and then fill this page) silver-plated copper powder and silver powder SF # 7 scaly zp average particle size 6.8 // m) 22.2 parts by weight of the polyamidamide polymer obtained by the synthesis of the above thermoplastic resin (B 1 ), diethylene glycol dimethyl ether 222.2 weight The varnish obtained by dissolving was dispersed by a disperser for 2 minutes to obtain a composition (paste) K. After defoaming the obtained paste, a certain amount was applied to a glass slide by screen printing (coating area: Lcmx 7.5 cm, coating thickness: 40 ± 10 0 / m), and drying in a batch drying oven at 180 ° C for 1 hour to obtain a dried coating film. The volume resistivity and migration characteristics of the obtained dried coating film were measured. The obtained paste was used to make a giant capacitor, and then the equivalent in-line resistance and leakage current were measured, and the edge wrapping property was evaluated. Example K2 The spherical copper powder obtained by the spray method had an average particle diameter of 5.9 // m, and was silver plated. The copper powder has an aspect ratio of 1.5 and an average particle size of 6.7. // m, other than the same embodiment K 1. Example K3 Ministry of Economic Affairs Intellectual Property Bureau employee consumption cooperative printed in addition to the spray method of the spherical copper powder average particle size of 5.9 / m, ball mill turnaround time For 60 minutes, the silver-plated copper powder has an aspect ratio of 2.5 and an average particle diameter of 8.0 // m, and the same as in the example K 1. Example K4 The average particle diameter of the spherical copper powder obtained by the spray method For 4.2 // m, the ball mill has a turnaround time of 1 20 minutes, the silver-plated copper powder has an aspect ratio of 12 and a flat paper scale for the Chinese National Standard (CNS) A4 specification (210X297 mm) -32- 1253457 A7 B7 V. Inventive Note (39 The average particle size is 7.2 // m, other examples are the same as in Example 1. (Please read the back note first and then fill in this page) Example K5 In addition to the spherical copper produced by the spray method The average particle size of the powder is 3.5 mM, the rotation time of the ball mill is 180 minutes, the aspect ratio of the silver-plated copper powder is 20, and the average particle diameter is 6.2 // m, and the other embodiment K 1 is implemented. Example K6 The spherical copper powder prepared by the spray method has an average particle diameter of 0.1 // m, and the silver-plated copper powder has an aspect ratio of 3.2 and The average particle size of the spherical copper powder prepared by the spray method is 〇. 6 // m, the length and width of the ore silver copper powder, except that the average particle diameter is 0.2//m. The ratio is 3 and the average particle size is 1.0 // m, and the other is the same as the embodiment K 1. Example K8 The Ministry of Economic Affairs Intellectual Property Office employee consumption cooperative prints the average particle size of the spherical copper powder obtained by the spray method. 1 . 〇# m ' The silver-plated copper powder has an aspect ratio of 3.1 and an average particle diameter of 1.5 megameters, and the other embodiment K 1 . Example K9 The average particle size of the spherical copper powder prepared by the spray method is 5. 5 # m ' -33- The paper size is applicable to the Chinese National Standard (CNS) A4 specification (210X297 mm) 1253457 A7 B7 Ministry of Economy Intellectual Property Bureau employee consumption cooperative printing 5, invention description (31) silver-plated copper powder aspect ratio of 3.1 and average particle size of 8.0 / m, the same as the embodiment K 1 . Example K 1 0 The spherical copper powder obtained by the spray method has an average particle diameter of 8.2 // m, and the silver-plated copper powder has an aspect ratio of 3.2 and an average particle diameter of 12 @ m. Example K1. Example K 1 1 The spherical copper powder obtained by the spray method has an average particle diameter of 1 3.6 // m, the silver-plated copper powder has an aspect ratio of 3.0 and an average particle diameter of 2 0 // m, and the like. Same as Example κ 1. Example κ 1 2 The spherical copper powder prepared by the spray method has an average particle diameter of 4.6 // m, the silver substitution amount to the spherical copper powder is 0.5% by weight, and the silver-plated copper powder has an aspect ratio of 3 5 and the average particle size is 6,7 #:^, other examples are the same as Κ 1. Example K13 The spherical copper powder obtained by the spray method has an average particle diameter of 3.8 // m, the silver substitution amount to the spherical copper powder is 1.Q% by weight, and the silver-plated copper powder has an aspect ratio of 3 1 and the same as the average particle diameter of 5.3 v, other examples κ 1. Example K14 (Please read the note on the back and then fill out this page) Packing · This paper scale applies to China National Standard (CNS) M specification (2丨(1)97公羡-34- 1253457 A7 B7 V. Invention Description (Please Read the note on the back and fill in this page. The average particle size of the spherical copper powder prepared by the spray method is 3 6 # m, and the silver substitution amount of the spherical copper powder is 1.5% by weight. The aspect ratio is 3.5 and the average particle diameter is 5.2 // m, and other examples are the same as κ 1. Example K 1 5 The spherical copper powder obtained by the spray method has an average particle diameter of 4.3 #m, The substitution amount of silver for the spherical copper powder is 25% by weight, the aspect ratio of the silver-plated copper powder is 3, 4, and the average particle diameter is 6.2 //, and other examples are the same as κ 1. Example κ 1 6 The spherical copper powder obtained by the spray method has an average particle diameter of 5. 〇# m, the substitution amount of silver for the spherical copper powder is 35 wt%, and the aspect ratio of the silver-plated copper powder is 3.8 and average. The particle size is 7.5 // m, and the other is the same as the embodiment K 1. Example Κ 1 7 Ministry of Economic Affairs Intellectual Property Bureau employee consumption cooperative prints spherical copper powder prepared by spray method The average particle diameter was 4.7 #m, the substitution amount of silver for the spherical copper powder was 50% by weight, the aspect ratio of the silver-plated copper powder was 4. 〇 and the average particle diameter was 7.1 v❿, and the same as in the example K1. Example 8 1 8 The spherical copper powder obtained by the spray method has an average particle diameter of 5.9 // m, the silver substitution amount for the spherical copper powder is 20% by weight, and the silver-plated copper powder has an aspect ratio of 2.5 and The average particle size is 8.0# m, and the shape of silver powder (Teli Chemical TCG-1) is spherical and the average particle size is 2.0 // m. Others are the same as in the example Κ 1. The paper scale applies to the Chinese National Standard (CNS). A4 size (210X297 mm) -35- 1253457 A7 Γ--s - JL7_ V. Description of invention (3 present embodiment κ 1 9 (please read the note on the back and then fill out this page) In addition to the spray method The average particle size of the spherical copper powder is 5.9 # m, the substitution amount of silver for the spherical copper powder is 2% by weight, the aspect ratio of the silver-plated copper powder is 2 · 5 and the average particle diameter is 8. 〇β In addition, the other examples are the same as κ 1. Example K20 The spherical copper powder prepared by the spray method has an average particle diameter of 5.9 # m, and the silver substitution amount to the spherical copper powder is 2% by weight. The silver-plated copper powder has an aspect ratio of 2.5 and an average particle diameter of 8. 〇#❿, other examples κ 1. Example K21 The average particle diameter of the spherical copper powder prepared by the spray method is 5.9 / / m, the silver substitution amount of the spherical copper powder is 20% by weight, the aspect ratio of the ore silver copper powder is 2.5, and the average particle diameter is 8,0 // m, and the same as the embodiment K 1. Example K22 The Ministry of Economic Affairs' Intellectual Property Office employee consumption cooperative printed the spherical copper powder prepared by the spray method with an average particle size of 5.9 // m, and the spherical copper powder with a silver substitution of 2% by weight, silver-plated copper powder. The aspect ratio was 2.5 and the average particle diameter was 8. 〇//111, which was the same as in Example 5:1. Example K23 The spherical copper powder prepared by the spray method has an average particle diameter of 5.9 // m, and the silver substitution amount of the spherical copper powder is 20% by weight, and the aspect ratio of the silver-plated copper powder is the paper scale. Applicable to China National Standard (CNS) A4 specification (210X297 mm) -36- 1253457 A7 B7 V. Description of invention (2.5 and average particle size is 8. 〇em, other with the same embodiment K 1. Example K24 Read the note on the back and fill in this page. The average particle size of the spherical copper powder prepared by the spray method is 5.9 # m, and the silver substitution amount of the spherical copper powder is 20% by weight. The broad ratio was 2.5 and the average particle diameter was 8. 〇# ;^, otherwise the same as Example K 1. Example K25 The polyamidoximine polymer obtained in Synthesis Example 2 except the above thermoplastic resin (B 1 ) was used. The spherical copper powder obtained by the spray method has an average particle diameter of 5.9 // m, the silver substitution amount to the spherical copper powder is 15% by weight, and the silver-plated copper powder has an aspect ratio of 2.5 and an average particle diameter. The same as Example 8.0 except that it was 8.0 / / m. Example K26 Polyamine obtained by the synthesis example 2 of the above thermoplastic resin (B1) The yttrium imine polymer, the spherical copper powder prepared by the spray method has an average particle diameter of 4.4/m, the silver substitution amount to the spherical copper powder is 15% by weight, and the silver-plated copper powder has an aspect ratio of 3.2. And the average particle size is 6.5 // m, other examples are the same as the K1 ° Ministry of Economic Affairs Intellectual Property Bureau employee consumption cooperative printing comparison example K 1 The average particle size of the spherical copper powder obtained by the spray method is 13.8 # m The substitution amount of silver for the spherical copper powder is 15% by weight, the rotation time of the ball mill is 240 minutes, the aspect ratio of the silver-plated copper powder is 25, and the average particle diameter is 26 #1, which is the same as the embodiment K1. The paper scale applies to the Chinese National Standard (CNS) A4 specification (210X 297 mm) _ 1253457 Ministry of Economic Affairs Intellectual Property Bureau employee consumption cooperative printed A7 ____ B7 V. Invention description (3 bow comparison example K2 In addition to using the above thermoplastic resin (B 1 The polyamidoximine polymer obtained in Synthesis Example 2, the spherical copper powder obtained by the spray method has an average particle diameter of 1 3.8 // m, and the silver substitution amount to the spherical copper powder is 15 weight. %, the ball mill has a rotation time of 240 minutes, and the silver-plated copper powder has an aspect ratio of 25 and an average particle diameter. The same as Example K1 except for 26 / / m. Comparative Example K3 The same as Example K1 except that the spherical copper powder (Mitsui metal ore with MFP 11 10 average particle diameter 1.1 A m ) was substituted for the silver-plated copper powder. Comparative Example K4 was the same as Example K1 except that no silver powder was contained. Comparative Example K5 was the same as Example K1 except that silver-plated copper powder was not contained. The results obtained are shown in Table K1 and Table K2. Silver-copper powder (a2) silver-plated copper powder obtained in the production example (copper exposed area: 20%) 118.8 parts by weight and silver powder (SF #7 scaly average particle size 6.8 // m manufactured by Cousteau) 79.2 parts by weight To the 2.2 parts by weight of the polyamine polymer 2 obtained in Synthesis Example 1 of the thermoplastic resin (B 1 ), two are added (please read the back of the back sheet and fill in this page) ---------I ! -- In 111- ; ---binding

本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) -38 - 1253457 經濟部智慧財產局員工消費合作社印製 A7 ____ B7五、發明説明(3今 乙二醇二甲基醚2 22.2重量份溶解而得之淸漆中,以分散機 分散20分鐘後,得粘度2000mPa · s之組成物(膏)L。將所 得膏脫泡後,利用網版印刷法將一定量塗布於玻璃載片上 (塗布面積:lcmx7.5cm,塗布厚:40±10/zm),再利用間 歇式乾燥爐以1 8 0 °C乾燥1小時,得乾燥塗膜。測定所得乾 燥塗膜之體積電阻率。爲了測定膏粘度之經時變化,而將 部分膏移入500毫升聚容器中,再放置於30 °C之高溫槽中, 6個月後再度測定粘度,以算出變化率。又,評估所得膏之 焊接接者性。另外以該膏爲陰極製作組電谷益’目式驗纟干接 耐熱性。 實施例L2 除了製作鍍銀銅粉時之球磨機回轉時間爲60分鐘’所 得鍍銀銅粉之銅露出面積爲3 0%外,其他同實施例L 1。 實施例L3 除了製作鍍銀銅粉時之銀取代量爲1 5重量%,所得鍍銀 銅粉之銅露出面積爲40%外,其他同實施例L1。 實施例L4 除了製作鍍銀銅粉時之球磨機回轉時間爲80分鐘’所 得鍍銀銅粉之銅露出面積爲60%外,其他同實施例L3。 實施例L5 (請先閲讀背面之注意事項再填寫本頁) 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) -39- 1253457 Α7 Β7 五、發明説明(3乃 除了使用上述熱塑性樹脂(B 1 )之合成例2所得的聚醯 胺醯亞胺聚合物外,其他同實施例L2。 (請先閱讀背面之注意事項再填寫本頁) 比較例L 1 除了製作鍍銀銅粉時之銀取代量爲3 〇重量份,球磨機 之回轉時間爲20分鐘,所得鍍銀銅粉之銅露出面積爲0%外 ,其他同實施例L 1。 比較例L 2 除了不使用鍍銀銅粉,銀粉量爲198重量份外,其他同 實施例L 1。 比較例 除了以噴霧法所製得之球狀銅粉取代鍍銀銅粉外,其 他同實施例L 1。 以上所得結果如表L 1所示。 實施例Μ 1 經濟部智慧財產局員工消費合作社印製 將鍍銀銅粉(a 1 )之製作例所得的鍍銀銅粉1 1 8.8重量 份及銀粉(得庫撒公司製SF# 7鱗片狀平均粒徑6.8//m) 79.2重量份,加入上述熱塑性樹脂(B2 )之合成例1所得的 聚醯胺聚矽氧烷共聚物22.2重量份中加入二乙二醇二甲基 醚222.2重量份溶解而得的淸漆中,以分散機分散20分鐘後 ,得粘度2000mPa · s之組成物(膏)Μ。將所得膏脫泡後’ -40- 本紙張尺度適用中國國家標準(CNS ) Α4規格(210Χ297公釐) 1253457 A7 B7 經濟部智慧財產局員工消費合作社印製 五、發明説明(3号 利用網版印刷法將一定量塗布於玻璃載片上(塗布面積: lcmx 7.5cm,塗布厚:40土 10 // m ),再利用間歇式乾燥爐 以1 8 0 °C乾燥1小時,得乾燥塗膜。測定所得乾燥塗膜之體 積電阻率。又,使用所得之膏製作塗膜強度測定用試料’ 再測定塗膜強度。另外以該膏爲陰極製作鉅電容器(定格 電壓4V ),測定啓動試驗後之電容器特性,及確認電容器 破壞情形。 實施例M2 除了製作鑛銀銅粉時之球磨機回轉時間爲8 0分鐘’所 得鍍銀銅粉之長寬比爲6.8外,其他同實施例Ml。 實施例M3 除了製作鍍銀銅粉時之球磨機回轉時間爲1 20分鐘’所 得鍍銀銅粉之長寬比爲12外,其他同實施例Ml。 實施例M4 除了製作鍍銀銅粉時之球磨機回轉時間爲150分鐘,所 得鍍銀銅粉之長寬比爲19.3外,其他同實施例Ml。 實施例 除了使用上述熱塑性樹脂(B2 )之合成例2所得的聚 醯胺醯亞胺聚矽氧烷共聚物外,其他同實施例M2。 (請先閲讀背面之注意事項再填寫本頁) -裝.This paper scale applies to China National Standard (CNS) A4 specification (210X297 mm) -38 - 1253457 Ministry of Economic Affairs Intellectual Property Bureau employee consumption cooperative printed A7 ____ B7 V. Invention description (3 present ethylene glycol dimethyl ether 2 22.2 The lacquer obtained by dissolving in a weight fraction was dispersed in a dispersing machine for 20 minutes to obtain a composition (paste) L having a viscosity of 2000 mPa·s. After the obtained paste was defoamed, a certain amount was applied to the glass by a screen printing method. On-chip (coating area: lcm x 7.5 cm, coating thickness: 40 ± 10 / zm), and drying in a batch drying oven at 180 ° C for 1 hour to obtain a dried coating film. The volume resistivity of the obtained dried coating film was measured. In order to determine the change of the viscosity of the paste over time, a part of the paste was transferred into a 500 ml poly vessel, placed in a high temperature bath at 30 ° C, and the viscosity was measured again after 6 months to calculate the rate of change. Solder joints. In addition, the paste was used as the cathode to make the heat resistance of the group. The example L2 The ball mill rotation time was 60 minutes except for the silver-plated copper powder. The copper exposed area is 30%, and its The same as Example L1. Example L3 The same as Example L1 except that the silver substitution amount in the production of the silver-plated copper powder was 15% by weight, and the copper exposed area of the obtained silver-plated copper powder was 40%. Except for the silver ball-making copper powder, the ball mill rotation time is 80 minutes, and the copper exposed area of the obtained silver-plated copper powder is 60%. Others are the same as the embodiment L3. Example L5 (Please read the back note first and then fill in the page) This paper size is applicable to the Chinese National Standard (CNS) A4 specification (210X297 mm) -39- 1253457 Α7 Β7 5. Inventive Note (3) Polyimine oxime obtained in Synthesis Example 2 except the above thermoplastic resin (B 1 ) In addition to the imine polymer, the same as the same example L2. (Please read the back note first and then fill out this page) Comparative Example L 1 In addition to the silver-plated copper powder, the silver substitution amount is 3 〇 by weight, the ball mill turning time For 20 minutes, the copper exposed area of the obtained silver-plated copper powder was 0%, and the same as in the same example L 1. Comparative Example L 2 except that silver-plated copper powder was not used, and the amount of silver powder was 198 parts by weight, the same as in the same example L 1. The comparative example is prepared by the spray method. The spherical copper powder replaces the silver-plated copper powder, and the other is the same as the embodiment L 1. The above results are shown in Table L 1. Example Μ 1 Ministry of Economic Affairs Intellectual Property Bureau employee consumption cooperative printed silver-plated copper powder (a 1 (1) 8.8 parts by weight of silver-plated copper powder and silver powder (SF# 7 scaly average particle diameter 6.8/m) obtained by the production example, 79.2 parts by weight, and a synthetic example of the thermoplastic resin (B2) 1 2 parts by weight of the obtained polyamidamine polyoxyalkylene copolymer was added to a enamel paint obtained by dissolving 222.2 parts by weight of diethylene glycol dimethyl ether, and dispersed for 20 minutes in a dispersing machine to obtain a viscosity of 2000 mPa·s. Composition (paste) Μ. After degassing the obtained cream '-40- This paper scale is applicable to China National Standard (CNS) Α4 specification (210Χ297 mm) 1253457 A7 B7 Ministry of Economic Affairs Intellectual Property Bureau employee consumption cooperative printing 5, invention description (No. 3 using the screen version) A certain amount of the coating method was applied to a glass slide (coating area: lcmx 7.5 cm, coating thickness: 40 soil 10 // m), and dried in a batch drying oven at 180 ° C for 1 hour to obtain a dried coating film. The volume resistivity of the obtained dried coating film was measured, and the obtained film was used to prepare a sample for measuring the strength of the coating film, and the film strength was measured. Further, a giant capacitor (4 V constant voltage) was prepared using the paste as a cathode, and the test was started. Capacitor characteristics, and confirming the damage of the capacitor. Example M2 The ball mill rotation time was 80 minutes except for the production of the ore-copper copper powder. The aspect ratio of the obtained silver-plated copper powder was 6.8, and the same as in the example M1. In addition to the silver-plated copper powder, the ball mill rotation time is 1 20 minutes' The obtained silver-plated copper powder has an aspect ratio of 12, and the same as in the same embodiment M1. Example M4 except for the production of silver-plated copper powder The mill rotation time was 150 minutes, and the obtained silver-plated copper powder had an aspect ratio of 19.3, which was the same as in Example M1. Examples of the polyamidoximine obtained by the synthesis of the above thermoplastic resin (B2) In addition to the alkane copolymer, the same as the same example M2. (Please read the back note first and then fill out this page) - Pack.

、1T, 1T

本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 1253457 Α7 Β7 五、發明説明(3弓 比較例Μ 1 除了製作鍍銀銅粉時之球磨機回轉時間爲1 8 〇分鐘,所 得鍍銀銅粉之長寬比爲2 3 . 〇外,其他同實施例Μ 1。 (請先閲讀背面之注意事項再填寫本頁) 比較例M2 除了使用上述熱塑性樹脂(Β 1 )之合成例i所得的聚 醯胺聚合物取代聚醯胺聚砂氧院共聚物外,其他同實施例 M2 〇 比較例Μ 3 除了以長寬比3 . 5之銀粉取代鍍銀銅粉外,其他同實施 例Μ 1。 比較例Μ4 除了以長寬比1之銅粉取代鍍銀銅粉外,其他同實施例This paper scale applies to China National Standard (CNS) A4 specification (210X297 mm) 1253457 Α7 Β7 V. Invention description (3 bow comparison example Μ 1 In addition to making silver-plated copper powder, the ball mill rotation time is 18 〇 minutes, the resulting plating The aspect ratio of the silver-copper powder is 2 3 . In addition, the same as in the example Μ 1. (Please read the note on the back side and then fill out this page) Comparative Example M2 In addition to the synthesis example using the above thermoplastic resin (Β 1 ) The obtained polyamine polymer was substituted for the polyamine polyoxalate copolymer, and the other example M2 〇 Comparative Example Μ 3 except for the silver-plated copper powder replaced by the silver powder having an aspect ratio of 3.5, the same example Μ 1. Comparative Example 4 except that silver-plated copper powder was replaced by copper powder of aspect ratio 1, the same example

Ml。 比較例M5 經濟部智慧財產局員工消費合作社印製 除了以環氧樹脂(三井化學(股)製,商品名140C) 60重 量份、脂肪族二縮水甘油醚(旭電化工業(股)製,商品名 ED-5 03 ) 40重量份、2P4MHZ (四國化成(股)製,硫唑)3重 量份及二胺二醯胺(和光純藥工業(股))3重量份取代聚醯 胺聚矽氧烷共聚物外,其他同實施例M2。 所得結果如表Μ 1所示。 -42 - 本紙張尺度適用中國國家標準(CNS ) Α4規格(21〇&gt;&lt;297公釐) 1253457 A7 B7 經濟部智慧財產局員工消費合作社印製 五、發明説明(, 實施例N 1 將鍍銀銅粉(a2 )製作例所得之鍍銀銅粉(銅露出面 積3 0% ) 1 1S. 8重量份及銀粉(得庫撒公司製 SF # 7 鱗 片狀 平均粒徑6.8 // m ) 79.2重量份,加入上述熱塑性樹 脂(B2)之合成例1所得的聚醯胺聚矽氧烷共聚物22.2重量 份中添加二乙二醇二甲基醚222.2重量份溶解而得的淸漆中 ,以分散機分散20分鐘後,得粘度2000mPa · s之組成物( 膏)N。將所得膏脫泡後,利用網版印刷法將一定量塗布於 玻璃載片上(塗布面積:lcmx 7.5cm,塗布厚:40± 10//m) ,再利用間歇式乾燥爐以180 °C乾燥1小時,得乾燥塗膜。 測定所得乾燥塗膜之體積電阻率。又,測定所得膏之撓性 。另外以該膏組成物爲陰極製作鉅電容器,再測定熱衝撃 性試驗後之電容器的漏電流(LC )。 實施例N2 除了使用熱塑性樹脂(B2 )之合成例2所得的聚醯胺醯 亞胺聚矽氧烷共聚物外,其他同實施例N 1。 實施例N3 除了使用熱塑性樹脂(B2 )之合成例2所得的聚醯胺醯 亞胺聚矽氧烷共聚物,製作鍍銀銅粉時之銀取代量爲1 5重 量%,球磨機之回轉時間爲80分鐘,所得鍍銀銅粉之銅露 出面積爲50%外,其他同實施例N1。 (請先閱讀背面之注意事項再填寫本頁) -裝_ 訂Ml. Comparative Example M5 Printed by the Ministry of Economic Affairs, the Intellectual Property Office, and the Consumers' Cooperative, in addition to epoxy resin (Mitsui Chemical Co., Ltd., trade name 140C), 60 parts by weight, aliphatic diglycidyl ether (asahi Chemical Industry Co., Ltd., commodity ED-5 03 ) 40 parts by weight, 2P4MHZ (Shikoku Chemical Co., Ltd., azolidine) 3 parts by weight and diamine diamine (Wako Pure Chemical Industries Co., Ltd.) 3 parts by weight of substituted polyamine polyfluorene Other than the oxyalkylene copolymer, the same as in the example M2. The results obtained are shown in Table 1. -42 - This paper size is applicable to China National Standard (CNS) Α4 specification (21〇&gt;&lt;297 mm) 1253457 A7 B7 Ministry of Economic Affairs Intellectual Property Bureau Employees Consumption Cooperative Printed V. Invention Description (Example N 1 Silver-plated copper powder (a2) silver-plated copper powder (copper exposed area of 30%) 1 1S. 8 parts by weight and silver powder (SF #7 scaly average particle size 6.8 // m made by Cousteau) 79.2 parts by weight of a phthalocyanine obtained by dissolving 222.2 parts by weight of diethylene glycol dimethyl ether added to 22.2 parts by weight of the polyamidamine polyoxyalkylene copolymer obtained in Synthesis Example 1 of the above thermoplastic resin (B2). After dispersing for 20 minutes in a dispersing machine, a composition (paste) N having a viscosity of 2000 mPa·s was obtained. After defoaming the obtained paste, a certain amount was applied to a glass slide by screen printing (coating area: lcmx 7.5 cm, coating) Thickness: 40 ± 10 / / m), and then dried in a batch drying oven at 180 ° C for 1 hour to obtain a dried coating film. The volume resistivity of the obtained dried coating film was measured. Further, the flexibility of the obtained paste was measured. The paste composition is a cathode for making a giant capacitor, and then measuring the thermal flushing property. Leakage current (LC ) of the capacitor after the test. Example N2 The same procedure as in Example N 1 except that the polyamidoximine polyoxyalkylene copolymer obtained in Synthesis Example 2 of the thermoplastic resin (B2) was used. N3 In addition to the polyamidoximine polyoxyalkylene copolymer obtained in Synthesis Example 2 of the thermoplastic resin (B2), the silver substitution amount in the production of the silver-plated copper powder was 15% by weight, and the rotation time of the ball mill was 80 minutes. The copper exposed copper powder has an exposed area of 50%, and the other is the same as the embodiment N1. (Please read the back note first and then fill in the page) - Install _

本紙張尺度適用中國國家標準(CNS ) A4規格(2丨0'〆297公釐) -43- 1253457 A7 B7 五、發明説明(41) 比較例N 1 (請先閲讀背面之注意事項再填寫本頁) 除了製作鍍銀銅粉時之銀取代量爲3 0重量% ’球磨機 之回轉時間爲20分鐘,所得鍍銀銅粉之銅露出面積爲〇% 外,其他同實施例N 1。 比較例N2 除了以環氧樹脂(三井化學(股)製,商品名140C ) 60重 量份、脂肪族二縮水甘油醚(旭電化工業(股)製,商品名 ED-5 03 ) 40重量份、2P4MHZ (四國化成(股)製,硫唑)3重 量份及二胺二醯胺(和光純藥工業(股))3重量份取代聚醯 胺聚矽氧烷共聚物外,其他同實施例N1。 所得結果如表N1所示。 本說明書所揭示,與200 1年10月19日所申請之特願 2001-3 22 320 號、2001 年 10 月 19日所申請之特願 200 1-322321 號、2001年10月31日所申請之特願200 1 -333649號及2001年 10月31日所申請之特願200 1 -333650號所記載之主題有關, 且引用其揭示內容。 經濟部智慧財產局員工消費合作社印製 除了上述外,不離開本發明之新穎且有利的特徵下, 可修正或變更上述實施形態。因此,申請範圍包括所有的 修正及變更內容。 本紙張尺度適用中國國家標準(CNS ) A4規格(210 X 297公釐) -44- 1253457 A7 B7 五、發明説明(叼 [表 K1] 經濟部智慧財產局員工消費合作社印製 添加表 鍍銀銅粉 長寬比 鍍銀銅粉 (重量份) 銀粉 (重量份) 樹脂 (重量份) 有機溶劑 (重量份) 實施例K1 1.3 100 100 22.2 222.2 實施例K2 1.5 100 100 22.2 222.2 實施例K3 2.5 100 100 22.2 222.2 實施例K4 12 100 100 22.2 222.2 實施例K5 20 100 100 22.2 222.2 實施例K6 3.2 100 100 22.2 222.2 實施例K7 3 100 100 22.2 222.2 實施例K8 3.1 100 100 22.2 222.2 實施例K9 3.1 100 100 22.2 222.2 實施例K10 3.2 100 100 22.2 222.2 實施例K11 3 100 100 22.2 222.2 實施例K12 3.5 100 100 22.2 222.2 實施例K13 3.1 100 100 22.2 222.2 實施例K14 3.5 100 100 22.2 222.2 實施例K15 3.4 100 100 22.2 222.2 實施例K16 3.8 100 100 22.2 222.2 實施例K17 4 100 100 22.2 222.2 實施例K18 2.5 100 100 22.2 222.2 實施例K19 2.5 100 25 13.8 222.2 實施例K20 2.5 100 42.8 15.9 222.2 實施例K21 2.5 100 66.6 18.5 222.2 實施例K22 2.5 100 150 27.8 222.2 實施例K23 2.5 100 233.3 37 222.2 實施例K24 2.5 100 400 55.6 222.2 實施例K25 2.5 100 100 22.2 222.2 實施例K26 3.2 100 100 22.2 222.2 比較例K1 25 100 100 22.2 222.2 比較例K2 25 100 100 22.2 222.2 比較例K3 1(銅粉) 1(銅粉) 100 22.2 222.2 比較例K4 1.3 200 0 22.2 222.2 比較例K5 - 0 200 22.2 222.2 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) (請先閱讀背面之注意事項再填寫本頁) -45- 1253457This paper scale applies to Chinese National Standard (CNS) A4 specification (2丨0'〆297 mm) -43- 1253457 A7 B7 V. Invention description (41) Comparative example N 1 (Please read the notes on the back and fill in the form) Page) The silver substitution amount was 30% by weight in the preparation of the silver-plated copper powder. The turning time of the ball mill was 20 minutes, and the copper exposed area of the obtained silver-plated copper powder was 〇%. Comparative Example N2 40 parts by weight of an epoxy resin (manufactured by Mitsui Chemicals Co., Ltd., trade name: 140C), 40 parts by weight of an aliphatic diglycidyl ether (manufactured by Asahi Kasei Co., Ltd., trade name: ED-5 03), 2P4MHZ (manufactured by Shikoku Kasei Co., Ltd., azole) 3 parts by weight and diamine diamine (Wako Pure Chemical Industries, Ltd.) 3 parts by weight of a substituted polyamine polyoxyalkylene copolymer, other examples N1. The results obtained are shown in Table N1. The application disclosed in this specification, with the special wishes of 2001-3 22 320, which were applied for on October 19, 2001, and the special wishes of the company, No. 200 1-322321, applied on October 19, 2001, and October 31, 2001. It is related to the subject matter described in Japanese Patent Application No. 2001-333650, the entire disclosure of which is hereby incorporated by reference. Printed by the Ministry of Economic Affairs, Intellectual Property Office, Employees' Consumer Cooperatives In addition to the above, the above embodiments may be modified or modified without departing from the novel and advantageous features of the present invention. Therefore, the scope of the application includes all amendments and changes. This paper scale applies to China National Standard (CNS) A4 specification (210 X 297 mm) -44- 1253457 A7 B7 V. Invention Description (叼 K1] Ministry of Economic Affairs Intellectual Property Bureau Staff Consumer Cooperative Printed Table Silver Plated Copper Powder aspect ratio silver-plated copper powder (parts by weight) Silver powder (parts by weight) Resin (parts by weight) Organic solvent (parts by weight) Example K1 1.3 100 100 22.2 222.2 Example K2 1.5 100 100 22.2 222.2 Example K3 2.5 100 100 22.2 222.2 Example K4 12 100 100 22.2 222.2 Example K5 20 100 100 22.2 222.2 Example K6 3.2 100 100 22.2 222.2 Example K7 3 100 100 22.2 222.2 Example K8 3.1 100 100 22.2 222.2 Example K9 3.1 100 100 22.2 222.2 Example K10 3.2 100 100 22.2 222.2 Example K11 3 100 100 22.2 222.2 Example K12 3.5 100 100 22.2 222.2 Example K13 3.1 100 100 22.2 222.2 Example K14 3.5 100 100 22.2 222.2 Example K15 3.4 100 100 22.2 222.2 Example K16 3.8 100 100 22.2 222.2 Example K17 4 100 100 22.2 222.2 Example K18 2.5 100 100 22.2 222.2 Example K19 2.5 100 25 13.8 222.2 Example K20 2.5 100 42.8 15.9 222.2 Example K21 2.5 100 66.6 18.5 222.2 Example K22 2.5 100 150 27.8 222.2 Example K23 2.5 100 233.3 37 222.2 Example K24 2.5 100 400 55.6 222.2 Example K25 2.5 100 100 22.2 222.2 Example K26 3.2 100 100 22.2 222.2 Comparative Example K1 25 100 100 22.2 222.2 Comparative Example K2 25 100 100 22.2 222.2 Comparative Example K3 1 (copper powder) 1 (copper powder) 100 22.2 222.2 Comparative Example K4 1.3 200 0 22.2 222.2 Comparative Example K5 - 0 200 22.2 222.2 This paper scale applies to Chinese National Standard (CNS) A4 specification (210X297 mm) (please read the notes on the back and fill out this page) -45- 1253457

經濟部智慧財產局員工消費合作社印製Ministry of Economic Affairs, Intellectual Property Bureau, employee consumption cooperative, printing

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(請先閱讀背面之注意事項再填寫本頁) •裝· 訂 1253457 A7 B7 五、發明説明(4今 經濟部智慧財產局員工消費合作社印製 【η撇】 備考 聚醯胺 聚醯胺 聚醯胺 聚醯胺 聚醯胺醯亞胺 聚醯胺 聚醯胺 聚醯胺 S — 嘈讲 歌 与 ^ i η悔_ 坳娣 If 识 290 °C r-H τ—Η CO r—i CN1 〇〇 260 °C ι &lt; r-Ή CNl uo τ—Η 〇 CSI CSI r-H r—Η τ—Η r-H 〇〇 焊接接著性 ____________ 320 °C pq PQ PQ o PQ 1 1 Q 290 °C PQ PQ PQ PQ PQ 1 1 Q 260 °C PQ C &lt; PQ &lt; U 1 Q 230 °C &lt; &lt; &lt; PQ &lt; U Q 體積電阻率 (Ω · cm) 3.5x10—5 4.5xl0—5 5.1χ10&quot;5 5.5xl0&quot;5 4.7χ10&quot;5 2.5χ10—5 2.1χ10&quot;5 1 8.2x10-4 膏之經時安定 性粘度增加率 (%) 卜 卜 〇 卜 Η 銅露出 面積(%) ο 〇 僅銅粉 〇 Η 實施例LI 實施例L2 實施例L3 實施例L4 實施例L5 比較例L1 比較例L2 比較例L3(Please read the notes on the back and fill out this page) • Install · Book 1253457 A7 B7 V. Invention Description (4 Printed by the Intellectual Property Office of the Ministry of Economic Affairs, Employees' Consumption Cooperatives [η撇] Prepared Polyamide Polyamine Polyamide Amine Polyamide Polyamide Amidoxime Polyamide Polyamide Polyamine S — 嘈 歌 song and ^ i η _ 坳娣 If you know 290 °C rH τ—Η CO r—i CN1 〇〇260 ° C ι &lt; r-Ή CNl uo τ—Η 〇CSI CSI rH r—Η τ—Η rH 〇〇welding adhesion ____________ 320 °C pq PQ PQ o PQ 1 1 Q 290 °C PQ PQ PQ PQ PQ 1 1 Q 260 °C PQ C &lt; PQ &lt; U 1 Q 230 °C &lt;&lt;&lt;&lt; PQ &lt; UQ Volume resistivity (Ω · cm) 3.5x10—5 4.5xl0—5 5.1χ10&quot;5 5.5xl0&quot ;5 4.7χ10&quot;5 2.5χ10—5 2.1χ10&quot;5 1 8.2x10-4 Paste stability viscosity increase rate (%) Bu Bu Bu Bu copper exposed area (%) ο 〇 Only copper powder 〇Η Implementation Example LI Example L2 Example L3 Example L4 Example L5 Comparative Example L1 Comparative Example L2 Comparative Example L3

ffil— V (請先閲讀背面之注意事項再填寫本頁) -裝· 訂 本紙張尺度適用中國國家標準(CNS ) Α4規格(210'乂297公釐) - 47- 1253457 A7 B7 經濟部智慧財產局員工消費合作社印製 五、發明説明(岣 τ—Η o ο 〇 〇 〇 Cvl CO VD oo 寸 &gt; o ο 〇 〇 〇 T—Η y~i cn 寸 〇 £ ® I ijiiml IvP \ &lt; o ο 〇 〇 〇 τ—Η r—Η CNl CO 〇〇 o ο 〇 〇 〇 Ο Ο o τ—Η cn s s I® pr &gt; o ο 〇 〇 〇 ο Ο o Ο 〇 oo CN1 cn 〇 卜 UO CNl Cvl On οό § uS Ό CO CO VO 〇6 劁z if 翅g UTi U&quot;i U&quot;&gt; ITi to 寸 1 o 1 ο 1 ο 1 〇 1 〇 1 ο 1 ο 1 o 1 ο 1 〇 If · X X r—Η X τ—Η X Η X Η X r—Η X r-H X τ—Η X ▼.....i X 駟a m igpn 寸 ΟΟ CO oo 〇4 οα r—( CO oo uo ΟΟ 00 1 崎 CSI 'sd CNl 〇6 擊 擊 擊 馨 € 鱷 譲 擊 € 擊 € Φ 迦 伽 crx? 祕 祕 祕 祕 祕 齡 祕 祕 奪 m 祕 塵 Μ 酹 狴 m 狴 塵 灑 灑 灑 灑 塵 灑 疆w cn 〇〇 CS cn On 〇〇 CO CNI 〇〇 £ S _ 1/Ί 鹪 ur&gt; CO T—Η r—Η CN1 cn 寸 1—Η CN| CO 寸 un s S Γ—! -Η 孽 氧 孽 羣 掌 孽 辑 闺 鎰 鎰 鎰 鎰 鎰 1¾ 舾 U U U ΛΛ λλ J.J ^LA (請先閲讀背面之注意事項再填寫本頁) 本紙張尺度適用中國國家標準(CNS ) Α4規格(210Χ 297公釐) 裝-Ffil—V (Please read the note on the back and fill out this page) -Installation · The size of the paper is applicable to the Chinese National Standard (CNS) Α4 specification (210'乂297 mm) - 47- 1253457 A7 B7 Ministry of Economics Intellectual Property Bureau employee consumption cooperative printing 5, invention description (岣τ—Η o ο 〇〇〇Cvl CO VD oo inch&gt; o ο 〇〇〇T—Η y~i cn inch ® £ ® I ijiiml IvP \ &lt; o ο 〇〇〇τΗΗ rΗΗ CNl CO 〇〇o ο 〇〇〇Ο Ο o τ—Η cn ss I® pr &gt; o ο 〇〇〇ο Ο o Ο 〇oo CN1 cn 〇 U UO CNl Cvl On οό § uS Ό CO CO VO 〇6 劁z if wing g UTi U&quot;i U&quot;&gt; ITi to inch 1 o 1 ο 1 ο 1 〇1 〇1 ο 1 ο 1 o 1 ο 1 〇If · XX r —Η X τ—Η X Η X Η X r—Η X rH X τ—Η X ▼.....i X 驷am igpn inch ΟΟ CO oo 〇4 οα r—( CO oo uo ΟΟ 00 1 Saki CSI 'sd CNl 〇6 击打打馨 € crocodile sniper €€ Φ 迦加crx? Secret 秘秘秘秘秘秘 m Secret Μ 狴m 狴 洒 洒 w w CN 〇〇 On 〇〇CO CNI 〇〇£ S _ 1/Ί 鹪Ur&gt; CO T—Η r—Η CN1 cn inch 1—Η CN| CO inch un s S Γ—! -Η 孽 孽 孽 孽 孽 闺镒镒镒镒镒 ⁄ ⁄ U U U U U U U U λ λ λ λ J J J J J Read the notes on the back and fill out this page.) The paper size is applicable to the Chinese National Standard (CNS) Α4 specification (210Χ 297 mm).

、1T -48- 1253457, 1T -48- 1253457

7 B 49 五、發明説明( 經濟部智慧財產局員工消費合作社印製 鉅電容器之熱衝撃試驗LC(pA) 30⑻循環 10以下 10以下 10以下 8 CO 5000 2000循環 10以下 10以下 10以下 Τ—Η 1000 1000循環 10以下 10以下 10以下 〇 撓性試驗 1萬次以上 1萬次以上 1禹次以上 1萬次以上 cn 體積電阻率 〇 • G 4.0χ10'5 4.3χ10'5 6·2χ10·5 2.0χ10'5 ι.Οχίσ4 樹脂 聚醯胺聚矽氧烷共聚物 聚醯胺醯亞胺聚矽氧烷共聚物 聚醯胺醯亞胺聚矽氧烷共聚物 聚醯胺聚矽氧烷共聚物 環氧樹脂 銅露出面積 〇 實施例N1 實施例N2 實施例Ν3 比較例Ν1 比較例Ν2 (請先閲讀背面之注意事項再填寫本頁)7 B 49 V. INSTRUCTIONS (The Ministry of Economic Affairs, Intellectual Property Office, Staff and Consumers Cooperative, Printed Giant Capacitor, Thermal Crush Test LC(pA) 30(8) Cycle 10 or less 10 or less 10 or less 8 CO 5000 2000 Cycle 10 or less 10 or less 10 or less Τ-Η 1000 1000 cycles 10 or less 10 or less 10 or less 〇Flexibility test 10,000 times or more 10,000 times or more 1 time or more 10,000 times or more cn Volume resistivity 〇• G 4.0χ10'5 4.3χ10'5 6·2χ10·5 2.0 Χ10'5 ι.Οχίσ4 Resin Polyamine Polyoxyalkylene Copolymer Polyamidimide Polyoxane Copolymer Polyamidoquinone Polyoxane Copolymer Polyamine Polyoxane Copolymer Ring Oxygen resin copper exposed area 〇 Example N1 Example N2 Example Ν 3 Comparative Example 比较 1 Comparative Example Ν 2 (Please read the back note and then fill out this page)

LP 裝. 訂 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) -49- 1253457 A7 B7 五、發明説明( 圖式簡單說明 圖1爲,有關本發明電子零件之一實施形態的固體電解 電容器一例之模式剖面圖。 主要元件對照表 1陽極線 2陽極基體 3電介質氧化膜 4固體電解質層 5陰極層 6導電性接著劑 7導線框 8外裝樹脂 10固體電解電容器 51碳層 52導電體層 (請先閱讀背面之注意事項再填寫本頁) 裝· 訂 經濟部智慧財產局員工消費合作社印製 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) -50-LP Packing. The standard paper size is applicable to the Chinese National Standard (CNS) A4 specification (210X297 mm) -49- 1253457 A7 B7 V. Description of the Invention (Simplified illustration of Figure 1 is an embodiment of the electronic component of the present invention. A schematic cross-sectional view of an example of a solid electrolytic capacitor. Main component comparison table 1 anode wire 2 anode substrate 3 dielectric oxide film 4 solid electrolyte layer 5 cathode layer 6 conductive adhesive 7 wire frame 8 exterior resin 10 solid electrolytic capacitor 51 carbon layer 52 Conductor layer (please read the precautions on the back and fill out this page) Packing · Ministry of Economic Affairs Intellectual Property Bureau Staff Consumer Cooperative Printed Paper Size Applicable to China National Standard (CNS) A4 Specification (210X297 mm) -50-

Claims (1)

六、申請專利範圍 第91 ] 24 1 02號專利申請案 中文申請專利範圍修正本 民國93年]1月12日修正 1 . 一種導電性樹脂組成物,其係含有含長寬比]至20之 鍍銀銅粉(a 1 )及銀粉的導電性粉末(A 1 ),及具有由醯 胺基、酯基、醯亞胺基及醚基群中所選出]種以上之官能基 的熱塑性樹脂(B 1 ),及有機溶劑(C )。 2. —種導電性樹脂組成物’其係含有含表面一部分具有 銅露出部分之鍍銀銅粉(a2 )及銀粉的導電性粉末(A2 ), 及具有由醯胺基、酯基、醯亞胺基及醚基群中所選出1種以 上之官能基的熱塑性樹脂(B 1 ),及有機溶劑(C )。 3. 如申請專利範圍第1或2項之導電性樹脂組成物,其中 ,熱塑性樹脂(B 1 )爲由聚伸苯基醚醯胺、聚伸苯基醚醯 亞胺、聚伸苯基醚醯胺醯亞胺、聚伸苯基醯胺、聚伸苯基 醯亞胺、聚伸苯基醯胺醯亞胺、聚苯二甲基醯胺、聚苯二 甲基醯亞胺及聚苯二甲基醯胺醯亞胺群中所選出者。 4. 如申請專利範圍第1或2項之導電性樹脂組成物,其中 ,熱塑性樹脂(B 1 )爲具有下列一般式(I ): I^-- (讀先閱讀背面之注意事項再填寫本頁) *11 r線VI. Application for Patent Scope 91] 24 1 02 Patent Application Revision of Chinese Patent Application Scope Amendment of the Republic of China 93 Years] January 12 Revision 1. A conductive resin composition containing an aspect ratio] to 20 a silver-plated copper powder (a 1 ) and a conductive powder (A 1 ) of silver powder, and a thermoplastic resin having a functional group selected from the group consisting of a mercapto group, an ester group, a quinone imine group, and an ether group ( B 1 ), and an organic solvent (C). 2. A conductive resin composition comprising a conductive powder (A2) containing a silver-plated copper powder (a2) having a copper exposed portion on a surface thereof, and a silver powder, and having a mercapto group, an ester group, and a ruthenium group A thermoplastic resin (B 1 ) having one or more functional groups selected from the group consisting of an amine group and an ether group, and an organic solvent (C). 3. The conductive resin composition according to claim 1 or 2, wherein the thermoplastic resin (B 1 ) is a polyphenylene ether oxime, a polyphenylene phenyl sulfoxide, a polyphenylene ether Amidoxime, polyphenyleneamine, polyphenyleneimine, polyphenylene phthalimide, polyphthalene decylamine, polyphenylene quinone imine, and polyphenylene Selected from the group of dimethyl amidoxime imines. 4. The conductive resin composition according to claim 1 or 2, wherein the thermoplastic resin (B 1 ) has the following general formula (I): I^-- (Read the first note on the back and fill in the form) Page) *11 r line (式中:R]、R2、R3及IT各自獨立爲氫、低級烷基、低級烷 本紙張尺度適用中國國家摞準(CNS ) A4規格(210X 297公釐) 1253457 A8 B8 C8 D8 六、申請專利範圍 氧基或鹵原子;X噫單鍵 C〇-、-S〇2-、 _S〇- H \/ H 或 Rd I -Ο Ι 甴6 ,其中R5及R6各自獨立爲氫、低級烷基 基或苯基;Y爲 氟甲基 氯甲 -NH—C—Ar —C—ΝΗ- -NH- C— II 〇 〇 II cΛ^, N— C II 〇 或 〇〇 II丨丨 c c/\/3\ -N Ar'3 N-\/\/ c c II II 〇 〇 (請先閱·#背面之注意事項再填寫本頁) -裝--------訂-- ,其中Ar1爲芳香族之2價基;Ar2爲芳香族之3價基;Ar3爲芳 香族之4價基) ••線 所示重覆單位,及下列一般式(II ):(In the formula: R], R2, R3 and IT are each independently hydrogen, lower alkyl, lower alkane. The paper size is applicable to China National Standard (CNS) A4 specification (210X 297 mm) 1253457 A8 B8 C8 D8 VI. Application Patent range oxy or halogen atom; X 噫 single bond C 〇 -, -S 〇 2, _S 〇 - H \ / H or Rd I - Ο 甴 甴 6, wherein R 5 and R 6 are each independently hydrogen, lower alkyl Or phenyl; Y is fluoromethylchloromethyl-NH-C-Ar-C-ΝΗ--NH-C-II 〇〇II cΛ^, N-C II 〇 or 〇〇II丨丨cc/\/ 3\ -N Ar'3 N-\/\/ cc II II 〇〇 (please read the first note on the back of the page and fill in this page) - install -------- order --- where Ar1 is Aromatic 2-valent group; Ar2 is an aromatic trivalent group; Ar3 is an aromatic 4-valent group) •• Repeated units shown by the line, and the following general formula (II): ⑼ (式中,R7、Rs&amp; R9各自獨立爲低級烷基、低級烷氧基或鹵 原子;s、t及u各自獨立爲表示取代基數目的〇至4之整數;R7 、Rs及R9各自具有複數個鍵時,可各自相同或相異;X 2及X 3 本紙張尺度適用中國國家摞準(CNS ) A4規格(2]0Χ297公嫠) 1253457 A8 B8 C8 D8 RIC—R 「、申請專利範圍 各自獨立爲-0-或(9) (wherein R7, Rs&amp; R9 are each independently a lower alkyl group, a lower alkoxy group or a halogen atom; and s, t and u are each independently an integer representing from the number of substituents to 4; and R7, Rs and R9 each have When multiple keys are used, they may be the same or different; X 2 and X 3 are applicable to China National Standard (CNS) A4 specification (2]0Χ297 mm) 1253457 A8 B8 C8 D8 RIC-R ", patent application scope Each is independently -0- or ,其中1^°及11]1各自獨立爲氫原子、低級烷基、三氟甲基、 三氯甲基或苯基;Y同上述一般式(I)所定義) 所示重覆單位中至少一者之樹脂。 5. —種導電性樹脂組成物、其係含有含長寬比1至20之 鍍銀銅粉(a 1 )及銀粉的導電性粉末(A 1 ),及聚醯胺聚 矽氧樹脂、聚醯胺醯亞胺聚矽氧樹脂及聚醯亞胺聚矽氧樹 脂群中所選出的熱塑性樹脂(B2 ),及有機溶劑(C )。 6. —種導電性樹脂組成物,其係含有含表面一部分具有 銅露出部分之鍍銀銅粉(a 2 )及銀粉的導電性粉末(A 2 ), 及聚醯胺聚矽氧樹脂、聚醯胺醯亞胺聚矽氧樹脂及聚醯亞 胺聚矽氧樹脂群中所選出的熱塑性樹脂(B2 ),及有機溶 劑(C )。 7·如申請專利範圍第2或6項之導電性樹脂組成物,其中 ,鍍銀銅粉(a2 )之銅露出面積爲10至70%。 8·—種鉅電解電容器,其係於由鉅所形成之陽極基體上 ’形成含有鉅氧化膜、固體電解質層,及使用申請專利範 圍第Γ、2、5與6項中任何一項之導電性樹脂組成物而形成 的含有導電體層之陰極層。 ------------- ---:___. ^ -___ 本纸張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) ~裝 訂 線 (請先閱讀背面之注意事項再填寫本頁) 經濟部智慧財產局員工消費合itri印製Wherein 1^° and 11]1 are each independently a hydrogen atom, a lower alkyl group, a trifluoromethyl group, a trichloromethyl group or a phenyl group; Y is at least as defined in the above general formula (I) One of the resins. 5. A conductive resin composition comprising a conductive powder (A 1 ) comprising silver-plated copper powder (a 1 ) having an aspect ratio of 1 to 20 and silver powder, and polyamine polyoxyl resin, poly The thermoplastic resin (B2) selected from the group consisting of amidoxime polyoxyl resin and a polyamidene polyoxyl resin group, and an organic solvent (C). 6. A conductive resin composition comprising a conductive powder (A 2 ) comprising a silver-plated copper powder (a 2 ) having a copper exposed portion on a surface thereof, and a silver powder, and a polyamine polyoxyl resin, a poly The thermoplastic resin (B2) selected from the group consisting of amidoxime polyoxyl resin and a polyamidene polyoxyl resin group, and an organic solvent (C). 7. The conductive resin composition according to claim 2 or 6, wherein the silver-plated copper powder (a2) has an exposed area of copper of 10 to 70%. 8. A giant electrolytic capacitor which is formed on an anode substrate formed by a giant body to form a conductive film containing a giant oxide film, a solid electrolyte layer, and using any one of the patent applications, items 2, 5 and 6. A cathode layer containing a conductor layer formed of a resin composition. ------------- ---:___. ^ -___ This paper size applies to Chinese National Standard (CNS) A4 specification (210X297 mm) ~ Gutter (please read the back of the note first) Matters to fill out this page) Ministry of Economic Affairs, Intellectual Property Bureau, employee consumption, itri printing
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US10629323B2 (en) * 2015-08-28 2020-04-21 Dupont Electronics, Inc. Electrically conductive adhesives
CN107922800B (en) 2015-08-28 2020-02-28 杜邦公司 Coated copper particles and uses thereof
US10611931B2 (en) 2015-08-28 2020-04-07 Dupont Electronics, Inc. Electrically conductive adhesives
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IT201800021346A1 (en) 2018-12-28 2020-06-28 Enrico Luigi Seveso Hot-melt resin to dissipate heat, electrically non-conductive and / or electrically insulating.
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