TW201026812A - Antistatic high temperature-resistant polyimide tape - Google Patents
Antistatic high temperature-resistant polyimide tape Download PDFInfo
- Publication number
- TW201026812A TW201026812A TW98100778A TW98100778A TW201026812A TW 201026812 A TW201026812 A TW 201026812A TW 98100778 A TW98100778 A TW 98100778A TW 98100778 A TW98100778 A TW 98100778A TW 201026812 A TW201026812 A TW 201026812A
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- Taiwan
- Prior art keywords
- tape
- layer
- conductive
- conductive layer
- weight
- Prior art date
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- 229920001721 polyimide Polymers 0.000 title claims abstract description 13
- 239000004642 Polyimide Substances 0.000 title claims abstract description 8
- 239000000758 substrate Substances 0.000 claims abstract description 29
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 claims abstract description 14
- 239000010410 layer Substances 0.000 claims description 53
- 239000000203 mixture Substances 0.000 claims description 41
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- 239000000853 adhesive Substances 0.000 claims description 27
- 230000001070 adhesive effect Effects 0.000 claims description 27
- 239000011248 coating agent Substances 0.000 claims description 25
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 20
- 239000000463 material Substances 0.000 claims description 15
- 239000012790 adhesive layer Substances 0.000 claims description 12
- 229920001940 conductive polymer Polymers 0.000 claims description 9
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- 229920005989 resin Polymers 0.000 claims description 8
- 239000011347 resin Substances 0.000 claims description 8
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 claims description 7
- 239000008367 deionised water Substances 0.000 claims description 7
- 229910021641 deionized water Inorganic materials 0.000 claims description 7
- 239000003431 cross linking reagent Substances 0.000 claims description 6
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- CMBZEFASPGWDEN-UHFFFAOYSA-N argon;hydrate Chemical compound O.[Ar] CMBZEFASPGWDEN-UHFFFAOYSA-N 0.000 claims description 2
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- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
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- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
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- 229920000123 polythiophene Polymers 0.000 description 3
- MFAWEYJGIGIYFH-UHFFFAOYSA-N 2-[4-(trimethoxymethyl)dodecoxymethyl]oxirane Chemical compound C(C1CO1)OCCCC(C(OC)(OC)OC)CCCCCCCC MFAWEYJGIGIYFH-UHFFFAOYSA-N 0.000 description 2
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- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
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- MRELNEQAGSRDBK-UHFFFAOYSA-N lanthanum(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[La+3].[La+3] MRELNEQAGSRDBK-UHFFFAOYSA-N 0.000 description 2
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- HMUNWXXNJPVALC-UHFFFAOYSA-N 1-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C(CN1CC2=C(CC1)NN=N2)=O HMUNWXXNJPVALC-UHFFFAOYSA-N 0.000 description 1
- LTSWUFKUZPPYEG-UHFFFAOYSA-N 1-decoxydecane Chemical compound CCCCCCCCCCOCCCCCCCCCC LTSWUFKUZPPYEG-UHFFFAOYSA-N 0.000 description 1
- JOWBFITYYIZBFK-UHFFFAOYSA-N 2,2-bis(sulfanyl)acetamide Chemical compound NC(=O)C(S)S JOWBFITYYIZBFK-UHFFFAOYSA-N 0.000 description 1
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 1
- JECYNCQXXKQDJN-UHFFFAOYSA-N 2-(2-methylhexan-2-yloxymethyl)oxirane Chemical compound CCCCC(C)(C)OCC1CO1 JECYNCQXXKQDJN-UHFFFAOYSA-N 0.000 description 1
- WZFUQSJFWNHZHM-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)CC(=O)N1CC2=C(CC1)NN=N2 WZFUQSJFWNHZHM-UHFFFAOYSA-N 0.000 description 1
- JSGVZIPDZWVOGQ-UHFFFAOYSA-N 2-[bis(sulfanyl)amino]ethanol Chemical compound OCCN(S)S JSGVZIPDZWVOGQ-UHFFFAOYSA-N 0.000 description 1
- CIEMDIKTFOLQML-UHFFFAOYSA-N 2-amino-1-sulfanylethanol Chemical compound NCC(O)S CIEMDIKTFOLQML-UHFFFAOYSA-N 0.000 description 1
- LLBZPESJRQGYMB-UHFFFAOYSA-N 4-one Natural products O1C(C(=O)CC)CC(C)C11C2(C)CCC(C3(C)C(C(C)(CO)C(OC4C(C(O)C(O)C(COC5C(C(O)C(O)CO5)OC5C(C(OC6C(C(O)C(O)C(CO)O6)O)C(O)C(CO)O5)OC5C(C(O)C(O)C(C)O5)O)O4)O)CC3)CC3)=C3C2(C)CC1 LLBZPESJRQGYMB-UHFFFAOYSA-N 0.000 description 1
- JHRDMNILWGIFBI-UHFFFAOYSA-N 6-diazenyl-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(N=N)=N1 JHRDMNILWGIFBI-UHFFFAOYSA-N 0.000 description 1
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- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
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- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
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- CLHAOIOLCMPIRX-UHFFFAOYSA-N benzoic acid diphenylmethanone Chemical compound OC(=O)C1=CC=CC=C1.C=1C=CC=CC=1C(=O)C1=CC=CC=C1 CLHAOIOLCMPIRX-UHFFFAOYSA-N 0.000 description 1
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- 238000010979 pH adjustment Methods 0.000 description 1
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- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
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- 235000011152 sodium sulphate Nutrition 0.000 description 1
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- PBCFLUZVCVVTBY-UHFFFAOYSA-N tantalum pentoxide Inorganic materials O=[Ta](=O)O[Ta](=O)=O PBCFLUZVCVVTBY-UHFFFAOYSA-N 0.000 description 1
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- Adhesive Tapes (AREA)
Abstract
Description
201026812 六、發明說明: 【發明所屬之技術領域】 本發明係關於一種膠帶’尤其關於一種防靜電的耐高 溫聚醯亞胺膠帶。 【先前技術】 • 隨著電子技術的飛速發展,積體電路物理尺寸逐步縮 小、集成度的不斷提高,以及更多新的高分子材料的廣泛 使用,靜電釋放日益變得重要,靜電防護問題也越來越受 10 到更爲廣泛的關注。其中印刷電路板(PCB )在過波峰焊 或回流焊工藝中需要高溫遮蔽膠帶,對其金手指及一些元 器件進行保護。例如,近年來無鉛回流焊的最高溫度達到 280°C-300°C。如果部分元器件比較靈敏,其容易被產生 的靜電所影響(在膠帶剝離PCB板過程中産生的靜電),因而 Φ #面要求冋/皿膠冑具有較好的耐高溫性,即S高溫後剝 離無殘膠,另一方面也要求耐高溫遮蔽膠帶具有防靜電功 問題: 一坚啊鬲溫防靜電膠帶仍然存在如 ⑴·向㈣切層與基材 劑,其導靜電性能主要㈣w料型添' 將無法發揮正常的二,"濕度’·在高溫環境 20 201026812 .向谬黏劑中引入導電金屬粒子或高分子微粒,儘 ^身可以保持導靜電魏,無縣靠環境巾的濕度, —:、表面或稍凸起的微米級導電顆粒由於直接接觸-些微 一( 方面可此引起短路;另一方面在膠帶剝離後 5可在器件表面留有少量導電粒子;導電顆粒的引入,將影 響膠黏劑本身的一些性能,如降低黏接強度、内聚強度等。 (3)·因向基材或底塗或膠層令的單獨或同時加入導電 • 物質,造轉帶的透光率明顯下降,不利於在PCB過高溫 後檢查膠層是否存在氣泡或殘膠等現象。 1〇 冑對上述問題,一些發明人提供下面的解決方案。如 美國專利公開第US2006025 1892Α1號公開了 一種防靜電單 面或雙面膠帶。這種膠帶的特徵在於在基材與膠層之間存 在一層導電底塗,該底塗包括導電金屬顆粒或導電聚合 物、聚丙烯或酚醛或橡膠樹脂、和交聯劑,通過一般的塗 15佈方式即可;底塗的塗佈厚度在0.5〜25微米範圍;該單面 膠帶的結構爲:膠層/導電底塗/基材;該雙面膠的結構爲膠 籲 導電底塗/基材/導電底膠層、膠層/導電底塗/基材/膠 層;該膠帶的膠系爲丙烯酸壓敏膠;但該膠帶不具備耐高 溫的性能; 20 美國專利1;85,631,079揭示一種耐高溫防靜電膠帶;該 膠帶的膠層爲含有粒徑低於1微米的表面導電包裹顆粒的 丙烯酸亞敏膠;該膠帶可浸泡在融化態金屬錫水(235t 〜265°C)至少5秒鐘後保持剝離無殘膠。 4 201026812 5 10 15 20 歐洲專利EP422919也公開了一種抗靜電耐高溫膠帶。 該膠帶包括基材、中間導電層(基材與膠層之間)、導電踢 層。基材包括耐高溫的聚醯亞胺薄膜。中間導電層爲含有 導電粒子的高分子塗層、或金屬真空渡層、或複合铭箔, 其表面電阻不低於1χ1〇7歐姆。導電膠層爲含有較大顆粒的 導電粒子’導電粒子甚至可以伸出膠面,將被接觸面與中 間導電層接通。當中間導電層使用鋁箔,膠系爲有機矽壓 敏膠時’矽底塗需要塗佈在鋁箔上之後再塗矽膠。此時可 以通過彎折鋁箔刺穿矽底塗及矽膠後,部分刺穿點直接接 觸被黏物而導通即起到防靜電作用,因而膠層中無須加入 任何導電顆粒。但當在較大張力的情況下,上述彎折易恢 復’刺穿點將失效’從而失去靜電功能。 此外,美國專利US5,637,368揭示了一種耐高溫防靜電 膠帶。該膠帶的結構爲(按順序):聚醯亞胺膜/五氧化二礬 塗層/矽底塗/矽膠。五氧化二礬塗層通過使用水性五氧化二 礬分散液(含帶有磺酸基團的聚合物)由特定的塗佈方式完 成。五氧化二蓉是不透明物質。 综上所述,上述專利所揭示的耐高溫防靜電膠帶雖然 在-定程度上滿足了对高溫與抗靜電的功能,但都沒有同 時克服上面描述的問題。 種能夠同時消除上述問題的耐高 因此’有必要開發一 溫防靜電膠帶。 【發明内容】 5 201026812 胺膠ί發在於提供一種耐高温防靜電的聚醯亞 其不僅具有抗靜電性能和耐高溫性能的良好平 而且避免了由離子型添加劑和導電粒子導致的問題, 而且具有良好的透光率。 5 10 15 本發明提供了_種膠帶,其包括:包括兩個主 tr胺基材、塗佈於所述基材至少-個主表面的 的種導電聚合物的導電層、佈置於所述導電層上 氧烧底塗、和佈置^纽底塗上㈣氧絲合劑層。 根據本發明某些實施方式的膠帶具有良好抗靜電性 (例如’膠帶在剝離時生產的靜電壓低於刚伏特⑺)、 與基材接觸面料電粒子、耐高溫⑽如,可在·。C下耐 受10分鐘以上)、透光率好、易於製備(例如採用一般塗佈 方法製備)’因而具備優異的綜合性能。 本發明的膝帶尤其適用於PCB靈敏元器件過波峰焊或 回流焊的遮蔽。 • 【實施方式】 本發明中,除非特別指出,術語“膠帶,,並不限於帶 狀’還包括’例如片狀,和與應用場合相匹配的任何其他 2〇 形狀。 、 本發明提供了-種膠帶,其包括:包括兩個主表面的 聚醯亞胺基材、塗佈於所述基材至少一個主表面的包括至 少一種導電聚合物的導電層、佈置於所述導電層上的石夕氧 烷底塗、和佈置在矽氧烷底塗上的矽氧烷黏合劑層。 25 本發明中對於聚醯亞胺基材沒有任何限制,一般的用 6 201026812 於膠帶領域的聚醯亞胺基材都可以用在本發明中。 根據某些較佳的實施方式,本發明的膠帶中所述導電 聚合物選自聚噻吩、聚噻吩與聚乙烯苯磺酸絡合物 (PEDT/PSS)、聚苯胺、聚呋喃、聚苯磺酸、以及它們的各 5 種混合物中。 根據某些較佳的實施方式,本發明的膠帶中所述導電 聚合物占導電層總重量的20〜50重量。/。。 根據某些較佳的實施方式,本發明的膠帶中所述導電 ❹ 層還包括選自水性樹脂、交聯劑、分散劑、偶聯劑、摻雜 10 劑、去離子水/溶劑混合液、pH調節劑中的至少一種。其中 所述水性樹脂包括但不限於丙烯酸樹脂、聚氨酯、環氧樹 脂、酚醛樹脂、有機矽分散鱧或上述樹脂的改性樹脂。所 述水性樹脂較佳占導電層總重量的4〇〜70重量❶/。。所述交聯 劑包括但不限於三聚氰胺、兩或兩官能度以上的氮丙咬、 15 異氰酸酯或其預聚體。所述交聯劑較佳占導電層總重量的 1〜25重量%。所述偶聯劑例如爲矽烷類偶聯劑,如κΗ56〇, 0 KH550 ’其較佳占導電層總重量的0.1〜5重量%。所述摻雜 劑包括但不限於金屬鹽、路易斯酸、非質子極性溶劑(如二 甲基甲醯胺(DMF),二甲基乙醯胺(DMAC) ,N-甲基 20 吡烙烷酮(NMP)等)、和其混合物。所述摻雜劑較佳占導 電層總重量的0.1〜0.5重量%。所述pH調節劑包括但不限於 氨水、二甲基乙醇胺、和其混合物。所述pH調節劑較佳占 導電層總重量的0.1〜〇.2重量%。 根據某些較佳的實施方式,本發明的膠帶中所述導電 7 201026812 層的塗佈厚度爲0.1〜0.5微米,成本相對較低,這是本發明 膠帶的另一個突出的優點。 根據某些較佳的實施方式,本發明的膠帶中所述導電 層的表面電阻爲1χ1〇5〜q。 5 10 15 ❹ 20 根據某些較佳的實施方式,本發明的膠帶中使用的底 塗爲石夕氧烧底塗。如邁圖新材料集團(中國上海)的 SS4191,道康寧(中國上海)的7499(有機錫)、信越(中 華民國臺北)的KR-3006A。 根據某些較佳的實施方式,本發明膠帶的膠層中的矽 氧烷黏合劑爲縮合型(有機錫催化型)矽氧烷黏合劑。如邁 圖新材料集團的PSA61〇/518 '道康寧的 7406/7355/7566/280A。 上述膠帶的結構可擴展成雙面膠帶,兩面的結構可以 相同或不同。例如,可以在基材的兩面分別塗佈:包括至 少一種導電聚合物的導電層'佈置於所述導電層上的矽氧 烷底塗、和佈置在矽氧烷底塗上的矽氧烷黏合劑層。也可 以在基材的一側塗佈包括至少一種導電聚合物的導電層、 塗佈於所述導電層上㈣纽底塗、和佈置切氧烧底塗 上的矽氧烷黏合劑層,而在基材的另一側分別再塗矽氧烷 底塗、碎乳炫》黏合劑層。 本發明的膠帶可以在膠層上貼合有離型膜。 下面結合附圖和實施例對本發明進行詳細的描述。需 要扣出,34些詳細的描述並非對本發明保護範圍的限制。 本發明的保護範圍以所附的權利要求書爲准。本發明中, 8 201026812 除非特別指出’百分比、份數、比值等均以重量爲基準。 圖1顯示根據本發明膠帶的一個實施方式的結構示意 圖。圖1中’從下到上依次爲基材i、導電塗層2、底塗3 = 膠層4。 — 5 實施例: 縮寫與實物對照表: ❿201026812 VI. Description of the Invention: [Technical Field] The present invention relates to a tape', particularly to an antistatic high temperature resistant polyimide tape. [Prior Art] • With the rapid development of electronic technology, the physical size of integrated circuits is gradually shrinking, the integration level is increasing, and more new polymer materials are widely used, electrostatic discharge is becoming more and more important, and electrostatic protection problems are also More and more 10 to more widespread attention. Among them, printed circuit boards (PCBs) require high-temperature masking tape in the wave soldering or reflow soldering process to protect their gold fingers and some components. For example, in recent years, the maximum temperature of lead-free reflow has reached 280 ° C - 300 ° C. If some components are sensitive, they are easily affected by the generated static electricity (static electricity generated during the process of peeling off the PCB from the tape), so the Φ #面 requires 冋/ 胄 胄 has a good high temperature resistance, that is, after S high temperature Peel-free adhesive residue, on the other hand, it also requires high-temperature masking tape to have anti-static work problem: A strong anti-static tape still exists as (1)·to (four) cut layer and substrate agent, its electrostatic conductivity is mainly (four) w material type Tim' will not be able to play normal two, "humidity" in high temperature environment 20 201026812. Introduce conductive metal particles or polymer particles into the adhesive, keep the static electricity, and the humidity of the environmental towel , --:, surface or slightly raised micron-sized conductive particles due to direct contact - some micro-one (this can cause short circuit; on the other hand, after the tape is peeled off 5, a small amount of conductive particles can be left on the surface of the device; the introduction of conductive particles, Will affect some properties of the adhesive itself, such as reducing the bonding strength, cohesive strength, etc. (3) · due to the substrate or primer or adhesive layer alone or simultaneously add conductive materials, turn belt The light transmittance is significantly reduced, which is not conducive to checking whether there is air bubbles or residual glue in the adhesive layer after the PCB is overheated. 1〇胄 For the above problems, some inventors provide the following solutions. For example, US Patent Publication No. US2006025 1892Α1 discloses An antistatic single-sided or double-sided tape characterized by the presence of a conductive undercoat between the substrate and the subbing layer comprising conductive metal particles or a conductive polymer, polypropylene or phenolic or rubber resin And a cross-linking agent, which can be applied by a general coating method; the coating thickness of the primer is in the range of 0.5 to 25 μm; the structure of the single-sided tape is: a rubber layer/conductive primer/substrate; The structure of the glue is a rubber-coated conductive primer/substrate/conductive primer layer, a glue layer/conductive primer/substrate/adhesive layer; the adhesive of the tape is an acrylic pressure-sensitive adhesive; but the tape does not have high temperature resistance. Performance; 20 US Patent 1; 85, 631, 079 discloses a high temperature resistant antistatic tape; the adhesive layer of the tape is an acrylic sub-sensitive adhesive containing surface conductive coated particles having a particle diameter of less than 1 micrometer; the tape can be immersed in a molten gold state Tin water (235t ~ 265 ° C) remains stripped without residue after at least 5 seconds. 4 201026812 5 10 15 20 European Patent EP 422 919 also discloses an antistatic high temperature resistant tape. The tape comprises a substrate, an intermediate conductive layer (base) Between the material and the adhesive layer, the conductive kick layer. The substrate comprises a high temperature resistant polyimide film. The intermediate conductive layer is a polymer coating containing conductive particles, or a metal vacuum layer, or a composite foil, the surface thereof The resistance is not less than 1χ1〇7 ohm. The conductive adhesive layer is a conductive particle containing larger particles. The conductive particles can even extend out of the rubber surface and connect the contact surface to the intermediate conductive layer. When the intermediate conductive layer uses aluminum foil, the adhesive system is used. For the organic enamel pressure sensitive adhesive, the enamel primer needs to be coated on the aluminum foil before the enamel is applied. At this time, after the punctured aluminum foil is pierced and the enamel is applied, the puncturing point directly contacts the adherend and conducts the anti-static effect, so that no conductive particles need to be added in the adhesive layer. However, in the case of a large tension, the above-mentioned bending is easy to recover, and the piercing point will fail, thereby losing the electrostatic function. In addition, U.S. Patent No. 5,637,368 discloses a high temperature resistant antistatic tape. The structure of the tape is (in order): polyimine film / tantalum pentoxide coating / enamel coating / silicone. The antimony pentoxide coating is formed by a specific coating method by using an aqueous pentoxide pentoxide dispersion (containing a polymer having a sulfonic acid group). Bismuth pentoxide is an opaque substance. In summary, the high temperature antistatic tape disclosed in the above patents satisfies the functions of high temperature and antistatic to a certain extent, but does not simultaneously overcome the problems described above. The high resistance that can eliminate the above problems at the same time makes it necessary to develop a temperature antistatic tape. SUMMARY OF THE INVENTION 5 201026812 Amine adhesive is to provide a high temperature and antistatic antimony. It not only has good antistatic property and high temperature resistance, but also avoids problems caused by ionic additives and conductive particles, and has Good light transmittance. 5 10 15 The present invention provides an adhesive tape comprising: a conductive layer comprising two main tr amine substrates, a conductive polymer coated on at least one major surface of the substrate, disposed on the conductive The layer is coated with an oxygen-fired primer, and the layer is coated with a (four) oxygen wire mixture layer. The tape according to some embodiments of the present invention has good antistatic properties (e.g., 'the static voltage produced by the tape when peeled off is less than just volts (7)), the contact with the substrate with the electrical particles of the fabric, and the high temperature resistance (10), for example. It is resistant to 10 minutes or more at C), has good light transmittance, and is easy to prepare (for example, prepared by a general coating method) and thus has excellent overall properties. The knee strap of the present invention is particularly suitable for over-wave soldering or reflow soldering of PCB sensitive components. • [Embodiment] In the present invention, unless otherwise specified, the term "adhesive tape, not limited to a belt shape" also includes, for example, a sheet shape, and any other shape that matches the application. The present invention provides - An adhesive tape comprising: a polyimide substrate comprising two major surfaces, a conductive layer comprising at least one conductive polymer coated on at least one major surface of the substrate, and a stone disposed on the conductive layer The base layer of the oxoxane and the layer of the argon oxide adhesive disposed on the base of the siloxane. 25 In the present invention, there is no limitation on the substrate of the polyimide, and the general use of 6 201026812 in the field of tape Amine substrates can be used in the present invention. According to certain preferred embodiments, the conductive polymer in the tape of the present invention is selected from the group consisting of polythiophene, polythiophene and polyvinylbenzenesulfonic acid complex (PEDT/PSS). , polyaniline, polyfuran, polybenzenesulfonic acid, and a mixture of each of them. According to certain preferred embodiments, the conductive polymer in the tape of the present invention accounts for 20 to 50 of the total weight of the conductive layer. Weight. /. According to In some preferred embodiments, the conductive ruthenium layer in the adhesive tape of the present invention further comprises an aqueous resin, a crosslinking agent, a dispersant, a coupling agent, a doping agent, a deionized water/solvent mixture, and a pH adjustment. At least one of the agents, wherein the aqueous resin includes, but is not limited to, an acrylic resin, a polyurethane, an epoxy resin, a phenol resin, an organic germanium dispersion, or a modified resin of the above resin. The aqueous resin preferably accounts for the total weight of the conductive layer. The crosslinking agent includes, but is not limited to, melamine, two or more functional nitrogen-acrylic nitriles, 15 isocyanate or a prepolymer thereof. The crosslinking agent preferably occupies a conductive layer. The coupling agent is, for example, 1 to 25% by weight of the total amount of the coupling agent, such as decane-type coupling agent, such as κΗ56〇, 0 KH550', which preferably accounts for 0.1 to 5% by weight based on the total weight of the conductive layer. However, it is not limited to metal salts, Lewis acids, aprotic polar solvents (such as dimethylformamide (DMF), dimethylacetamide (DMAC), N-methyl 20 pyrrolidone (NMP), etc.), And a mixture thereof. The dopant preferably accounts for the total weight of the conductive layer The pH adjusting agent includes, but not limited to, ammonia water, dimethylethanolamine, and a mixture thereof, and the pH adjusting agent preferably accounts for 0.1 to 0.2% by weight based on the total weight of the conductive layer. In some preferred embodiments, the conductive layer 7 201026812 of the tape of the present invention has a coating thickness of 0.1 to 0.5 μm and a relatively low cost, which is another outstanding advantage of the tape of the present invention. The surface resistivity of the conductive layer in the adhesive tape of the present invention is 1χ1〇5~q. 5 10 15 ❹ 20 According to some preferred embodiments, the primer used in the adhesive tape of the present invention is Shi Xi oxygen. Burning primers, such as SS4191 of Momentive New Materials Group (Shanghai, China), 7499 (organic tin) of Dow Corning (Shanghai, China), and KR-3006A of Shin-Etsu (Taipei, Republic of China). According to certain preferred embodiments, the siloxane adhesive in the adhesive layer of the tape of the present invention is a condensed (organotin catalyzed) decane adhesive. Such as the Momentive New Materials Group's PSA61〇/518 'Dow Corning's 7406/7355/7566/280A. The structure of the above tape can be expanded into a double-sided tape, and the structures on both sides can be the same or different. For example, it may be separately coated on both sides of the substrate: a conductive layer comprising at least one conductive polymer', a naphthenic primer disposed on the conductive layer, and a lanthanum oxide disposed on the undercoat of the siloxane. Agent layer. It is also possible to coat a conductive layer comprising at least one conductive polymer on one side of the substrate, a (4) neocoat coated on the conductive layer, and a layer of a phthalocyanine adhesive disposed on the oxy-oxygen primer. On the other side of the substrate, a layer of a buffer of a naphthenic base coat and a crushed emulsion was separately applied. The tape of the present invention may have a release film adhered to the adhesive layer. The invention will now be described in detail in conjunction with the drawings and embodiments. The detailed description is not intended to limit the scope of the invention. The scope of the invention is defined by the appended claims. In the present invention, 8 201026812 Unless otherwise specified, 'percentage, parts, ratio, etc. are based on weight. BRIEF DESCRIPTION OF THE DRAWINGS Figure 1 is a schematic view showing the structure of an embodiment of an adhesive tape according to the present invention. In Fig. 1, 'from bottom to top is substrate i, conductive coating 2, primer 3 = glue layer 4. — 5 Example: Abbreviation and physical comparison table: ❿
KH550 3-縮水甘油醚氧基丙基三甲 氧基矽烷KH550 3-glycidoxypropyltrimethoxydecane
DMFDMF
DMAC A-75 L-W75DMAC A-75 L-W75
BPO DCBPO .甲基曱酿胺 二曱基乙酿胺 吡烙烧鲖 75%的BPO與結晶水混合物 75%的BPO與結晶水混合物 過氧化二苯甲醯 2.4—一氣過氧化苯甲酿 國藥集團化學試劑有限公司 (分析純) 國藥集團化學試劑有限公司 (分析純) 國藥集團化學試劑有限公司 (分析純) ΐ7科瑪(常熟)化學:公司_ 阿克蘇諾貝爾中國,上海南 京西路1468號中欣大廈三樓 德固赛中國上海 9 201026812 ❿ D604 非離子氟類表面活性劑 1氣化工產品(中國)投資有 限公司 Sancure 825 HD-MB019 氨醋 丙烯酸酯 儿小金彙利應用化工製品有 限公司 DMAE 二曱基乙醇胺 國藥集團化學試劑有限公司 (分析純) BaytranP 聚噻酚與聚乙烯磺酸納的絡 合物 H.C.Stark,德國 A-187 3-縮水甘油醚氧丙基三甲氧 基矽烷 邁圖南新材料集團,地址: 上海市張江高科技園區李冰 路227號 50MD07 2rml透明氟素離型pet膜 Siliconenature 義大利 SILFLU 75MD07 W 3mil氟素離型PET白色不透 明膜 Siliconenature 義大利 Cymel 325 曱基醚化高亞氨基三聚氰胺 樹脂 美國氰特公司TSXS~ 測試方法: 5 一、 靜電耗散時間 1.測試者帶上靜電防護手套,將預先切好的i5〇mmx 201026812 150mm的樣品放入靜電耗散儀(Model 406C, ElectroTech Systems, Inc. (ETS))測試室; 2.將樣品表面電荷測試值歸零,給樣品瞬間加5000V 高壓; 5 3.按測試鍵,樣品外加電壓立即停止,記錄靜電耗 散時間;一般來說,如果超過30s即視爲絕緣性好, 手動停止測試;低於0.01S即爲具有導靜電功能。 二、 解卷靜電壓的測試 10 1.將膠帶(寬25mm,長33m,卷芯内徑爲76.2mm)放在 IMASS 測試儀(型號爲 SP-2000)上,以 2286mm/min 的速度解卷; 2.帶上靜電防護手套,手持3M718靜電測試儀,紅 外探測對準膠帶解卷的部位,測試解卷過程產生 15 的靜電壓。 三、 对南溫測試 1. 將25mm寬的膠帶貼合在2mm厚50mm X 150mm大 小的鋼板上,然後放入已升至280攝氏度高溫的烘 20 箱; 2. 10分鐘後立即取出鋼板,膠帶與鋼板間無氣泡、 魚眼,高溫剝離膠帶無殘膠;冷卻到室溫後剝離 亦無殘膠。 25 四、 透明度的評定標準 201026812 • 將膠帶貼在電路板(PCB)上’目視對膠帶透明度進行 評定,標準如下: 0: 完全不可見膠帶下面的元器件; 1: 隱約可見膠帶下面的元器件; 5 2: 清晰可見膠帶下面的元器件。 實例1 1.原材料 基材:6051 ’ 25微米厚的聚醯亞胺膜,由天幸市天緣電工 材料有限責任公司; 10 石夕氧烷底塗:SS4191(SS4191A、SS4191B、SS4192C、 SS4259C)由邁圖南新材料集團(上海)提供· 矽氧烷黏合劑: 7406,由道康寧提供(上海); A-75, 75%的BPO ;阿克蘇諾貝爾(常熟)提供; 導電塗層:BaytronP,由 H.C.Stark(德國); 5 Sancure 825,水性聚氨醋,由上海源禾化工提供; D604,非離子氟類表面活性劑,由空氣化工産品(中 國)投資有限公司(上海市); A-187,矽烷偶聯劑’由邁圖新材料集團提供(上海); NMP,試劑級; 20 二曱基乙醇胺,試劑級; 水,去離子水; 異丙醇,試劑級。 2·製備方法 25 2.1配方 12 201026812 A.導電塗層的配方: 表1導電塗層配方(單位:克)BPO DCBPO .Methyl-branched amine dimercapto-ethyl amide-pyro-burning 鲖 75% BPO and crystallization water mixture 75% BPO and crystallization water mixture benzoic acid benzophenone 2.4-one gas peroxide benzoic acid Chinese medicine group Chemical Reagent Co., Ltd. (analytical grade) Sinopharm Chemical Reagent Co., Ltd. (analytical grade) Sinopharm Chemical Reagent Co., Ltd. (analytical grade) ΐ7 Kema (Changshu) Chemistry: Company _ Akzo Nobel China, 1468 Nanjing West Road, Shanghai 3rd Floor, Xin Building, Shanghai, China 9 201026812 ❿ D604 Non-ionic Fluoride Surfactant 1 Gas Chemicals (China) Investment Co., Ltd. Sancure 825 HD-MB019 Ammonia vinegar acrylate Xiaojin Huili Applied Chemicals Co., Ltd. DMAE II Mercaptoethanolamine Sinopharm Chemical Reagent Co., Ltd. (analytical grade) BaytranP complex of polythiophene with sodium sulphate HCStark, Germany A-187 3-glycidyloxypropyltrimethoxydecane Motulnan New Materials Group, Address: No. 227, Libing Road, Zhangjiang Hi-Tech Park, Shanghai 50MD07 2rml transparent fluorinated release pet film Siliconeature Italy SILFLU 75MD07 W 3mil Fluorine-free PET white opaque film Siliconeature Italy Cymel 325 Mercapto etherification high imino melamine resin US Cytec TSXS~ Test method: 5 I. Static dissipative time 1. Tester with ESD gloves Put the pre-cut i5〇mmx 201026812 150mm sample into the static dissipative instrument (Model 406C, ElectroTech Systems, Inc. (ETS)) test room; 2. Zero the sample surface charge test value, and add the sample instantaneously. 5000V high voltage; 5 3. Press the test button, the applied voltage immediately stops, record the static dissipation time; in general, if it exceeds 30s, it is considered to be good insulation, manually stop the test; below 0.01S, it has the function of conducting static electricity. . Second, unwinding static voltage test 10 1. Place the tape (width 25mm, length 33m, core diameter 76.2mm) on the IMASS tester (model SP-2000), unwind at 2286mm/min 2. Bring the static protective gloves, hold the 3M718 static tester, and illuminate the area where the tape is unwound, and test the static voltage generated by the unwinding process. 3. Test on the south temperature 1. Lay the 25mm wide tape on the 2mm thick 50mm X 150mm steel plate, and then put it into the 20-box oven that has been raised to 280 degrees Celsius; 2. Remove the steel plate immediately after 10 minutes. There is no bubble between the steel plate and the fish eye, and the high temperature peeling tape has no residual glue; after cooling to room temperature, there is no residual glue after peeling off. 25 IV. Evaluation of Transparency 201026812 • Stick the tape on the circuit board (PCB). Visually assess the transparency of the tape. The standard is as follows: 0: The components under the tape are completely invisible; 1: The components under the tape are faintly visible. ; 5 2: Clearly visible components under the tape. Example 1 1. Raw material substrate: 6051 '25 μm thick polyimine film, by Tianxing Tianyuan Electric Material Co., Ltd.; 10 Shixioxane primer: SS4191 (SS4191A, SS4191B, SS4192C, SS4259C) Maitu South New Materials Group (Shanghai) offers · siloxane adhesive: 7406, supplied by Dow Corning (Shanghai); A-75, 75% BPO; Akzo Nobel (Changshu); Conductive coating: BaytronP, by HCStark (Germany); 5 Sancure 825, water-based polyurethane, supplied by Shanghai Yuanhe Chemical; D604, non-ionic fluorine surfactant, by Air Products (China) Investment Co., Ltd. (Shanghai); A-187 , decane coupling agent' provided by Momentive New Materials Group (Shanghai); NMP, reagent grade; 20 dimercaptoethanolamine, reagent grade; water, deionized water; isopropanol, reagent grade. 2. Preparation method 25 2.1 Formulation 12 201026812 A. Formulation of conductive coating: Table 1 Conductive coating formula (unit: gram)
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Baytran P 3.320 50% DMAE 0.096 NMP 0.218 去離子水 4.600 異丙醇 4.600 Sancure 825 0.570 正丁醇 0.250 A-187 0.003 D 604 0.008 固含量,% 1.00% 注:各原料依次加入,並邊攪拌邊慢慢加入; B.底塗配方: 表2矽氧烷底塗配方(單位:克) 丁酮 14.1 正庚烧 57.6 30% SS4191A 8 100% SS4191B 0.181 43% SS4192C 0.088 50% SS4259C 0.176 固含量, 3% C.膠配方 13 201026812 表3 7406矽氧烷黏合劑配方(單位:克) 7406 100 10% A-75 22.40 曱苯 30 共計: 152.40 固含量, 3 8% 2.2製備過程 將上述導電塗層混合液用250LPI絲網印刷輥塗於25 Φ 微米厚的聚醯亞胺面一側,並進烘箱烘乾,烘箱最高設置 5 溫度爲180°C。塗佈厚度控制在0.1〜0.5微米。接著在該導 電塗層上面塗佈0.1〜0.5微米厚的矽氧烷底塗並烘乾,最高 設置溫度爲140°C ;最後再在矽氧烷底塗上塗佈矽氧烷黏合 劑,並烘乾固化,塗膠厚度爲25〜30微米。 2.3性能 10 表4實例1的測試性能 性能 測試 測試方法 對鋼板的黏性:(等待 24h at 23C) 0.20 N/mm ASTMD-3330 拉伸強度 : 115 N/25mm ASTMD-882 斷裂伸長率: > 40 % 膠帶總厚度: 0.059 mm ASTMD-3652 擊穿電壓: 6.0 Kv ASTMD-149 靜電耗散時間: <0.01s 如前所述 産生靜電壓:解卷過程 <100 V 如前所述,90 in/min的解卷速 度 201026812 :從FPC剝離 <100 V 如前所述’ 90 in/min的解卷速 度 而才面溫 無殘膠、氣 泡 280°C lOmins 透明度 2 目視 實例2 1.原材料 基材:605卜25微米厚的聚醯亞胺膜,由天津市天緣電工 ® 5 材料有限責任公司; 矽氧烷底塗:SS4191(SS4191A,SS4191B、SS4192C、 SS4259C)由邁圖新材料集團提供; 矽氧烷黏合劑: 7355,由道康寧提供; A-75,阿克蘇諾貝爾提供; 10 DCBPO,德固賽提供; 導電塗層:Baytron P,由 H.C.Stark; HD-MB019,由北京金彙利應用化工製品有限公 φ 司提供; 325,由氰特公司提供; 15 D604,由美國空氣化學提供; A-187,由邁圖高新材料集團(上海)提供; NMP,試劑級; 二曱基乙醯胺,試劑級; 水,水離子水; 20 異丙醇,試劑級。 15 201026812 2.製備方法 2.1配方 A.導電塗層的配方: 表5導電塗層配方(單位:克)Baytran P 3.320 50% DMAE 0.096 NMP 0.218 Deionized water 4.600 Isopropanol 4.600 Sancure 825 0.570 n-butanol 0.250 A-187 0.003 D 604 0.008 Solids, % 1.00% Note: Add the ingredients in turn and slowly while stirring B. Primer formulation: Table 2: Naphthenic basecoating formula (unit: gram) Butanone 14.1 Zhenggeng 57.6 30% SS4191A 8 100% SS4191B 0.181 43% SS4192C 0.088 50% SS4259C 0.176 Solid content, 3% C Gel Formulation 13 201026812 Table 3 7406 Oxane Adhesive Formulation (Unit: gram) 7406 100 10% A-75 22.40 Toluene 30 Total: 152.40 Solid Content, 3 8% 2.2 Preparation Process The above conductive coating mixture is used A 250 LPI screen printing roll was applied to the side of a 25 Φ micron thick polyimide surface and dried in an oven with a maximum oven temperature of 180 °C. The coating thickness is controlled to be 0.1 to 0.5 μm. Then coating a 0.1~0.5 micron thick porphyrin undercoat on the conductive coating layer and drying, the maximum setting temperature is 140 ° C; finally, coating the decyl oxide primer on the bottom layer of the oxirane, and Drying and curing, the thickness of the glue is 25~30 microns. 2.3 Performance 10 Table 4 Test performance of Example 1 Performance test Test method Viscosity to steel plate: (waiting 24h at 23C) 0.20 N/mm ASTMD-3330 Tensile strength: 115 N/25mm ASTMD-882 Elongation at break: > 40 % total tape thickness: 0.059 mm ASTMD-3652 breakdown voltage: 6.0 Kv ASTMD-149 static dissipation time: <0.01s static voltage generated as previously described: unwinding process <100 V as previously described, 90 In/min unwinding speed 201026812: peeling from FPC <100 V As described above, '90 in/min unwinding speed, only face temperature without residue, bubble 280 °C lOmins transparency 2 Visual example 2 1. Raw materials Substrate: 605 25 μm thick polyimide film, by Tianjin Tianyuan Electrician® 5 Materials Co., Ltd.; 矽 底 底 :: SS4191 (SS4191A, SS4191B, SS4192C, SS4259C) by Momentive New Materials Group Provided; Alkane adhesive: 7355, supplied by Dow Corning; A-75, supplied by AkzoNobel; 10 DCBPO, supplied by Degussa; Conductive coating: Baytron P, by HCStark; HD-MB019, by Beijing Jinhui Li Applied Chemicals Co., Ltd. provides 256 Division; 325 Provided by Cytec; 15 D604, supplied by American Air Chemistry; A-187, supplied by Momentive New Materials Group (Shanghai); NMP, reagent grade; dimercaptoacetamide, reagent grade; water, water ionized water 20 isopropyl alcohol, reagent grade. 15 201026812 2. Preparation method 2.1 Formulation A. Formulation of conductive coating: Table 5 Conductive coating formula (unit: gram)
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Baytran P 6.600 50% DMAE 0.096 NMP 0.218 去離子水 5.000 異丙醇 5.000 HD-MD019 0.300 Cymel 325 0.080 正丁醇 0.250 A-187 0.003 D 604 0.008 固含量,% 1.04% 註:各原料依次加入,並邊授摔邊慢慢加入; B.底塗配方: 表6矽氧烷底塗配方(單位:克) 丁酮 14.1 正庚烷 57.6 30% SS4191A 8 100% SS4191B 0.181 43% SS4192C 0.088 50% SS4259C 0.176 固含量, 3% 16 201026812 C.膠配方 表7矽氧烷黏合劑配方(單位:克)Baytran P 6.600 50% DMAE 0.096 NMP 0.218 Deionized water 5.000 Isopropyl alcohol 5.000 HD-MD019 0.300 Cymel 325 0.080 n-butanol 0.250 A-187 0.003 D 604 0.008 Solids content, % 1.04% Note: The raw materials are added in sequence and B. Primer formulation: Table 6: Oxane basecoat formulation (unit: gram) Butanone 14.1 n-heptane 57.6 30% SS4191A 8 100% SS4191B 0.181 43% SS4192C 0.088 50% SS4259C 0.176 Solid Content, 3% 16 201026812 C. Glue Formulation Table 7 Oxane Adhesive Formulation (Unit: gram)
7355 100 10% A-75 22.40 曱苯 30 共計: 152.40 固含量, 3 8% 57355 100 10% A-75 22.40 toluene 30 Total: 152.40 Solids, 3 8% 5
2.2製備過程 與例1相同 2.3性能 表8實例2的測試性能 性能 測試 測試方法 對鋼板的黏性:(等待 24h at 23C) 0.28 N/mm ASTMD-3330 拉伸強度 : 115 N/25mm ASTMD-882 斷裂伸長率: >40 % 膠帶總厚度: 0.050 mm ASTMD-3652 擊穿電壓: 6.0 Kv ASTMD-149 靜電耗散時間: <0.01 S 如前所述 産生靜電壓:解卷過程 <100V 如前所述, 90 in/min的解卷速度 201026812 :從FPC剝離 <100V 如前所述, 90 in/min的解卷速度 而子南溫 無殘膠、氣 泡 280°C lOmins 透明度 2 目視 實例3 1.原材料 參 5 10 15 基材:605卜25微米厚的聚醯亞胺膜,由天津市天緣電工 材料有限責任公司; 矽氧烷底塗:SS4191(SS4191A、SS4191B、SS4192C、 SS4259C)由邁圖新材料集團(上海)提供; 矽氧烷黏合劑:7355,由道康寧(上海)提供; 7406,由道康寧(上海)提供; A-75,阿克瑪(常熟)提供; 導電塗層:Baytron P,由 H.C.Stark(德國); HD-MB019, 由北京金彙利應用化工製品有限 公司提供;2.2 Preparation process is the same as in Example 1. 2.3 Performance Table 8 Test performance of Example 2 Performance test Test method Viscosity to steel plate: (waiting 24h at 23C) 0.28 N/mm ASTMD-3330 Tensile strength: 115 N/25mm ASTMD-882 Elongation at break: > 40 % Total thickness of tape: 0.050 mm ASTMD-3652 Breakdown voltage: 6.0 Kv ASTMD-149 Static dissipative time: <0.01 S Static voltage generated as described above: unwinding process <100V As previously mentioned, 90 in/min unwinding speed 201026812: stripping from FPC <100V as previously described, 90 in/min unwinding speed while sub-small temperature without residue, bubble 280 ° C lOmins transparency 2 visual example 3 1. Raw material reference 5 10 15 Substrate: 605 25 μm thick polyimide film, by Tianjin Tianyuan Electrical Material Co., Ltd.; Oxygenane primer: SS4191 (SS4191A, SS4191B, SS4192C, SS4259C) Provided by Momentive New Materials Group (Shanghai); siloxane adhesive: 7355, supplied by Dow Corning (Shanghai); 7406, supplied by Dow Corning (Shanghai); A-75, supplied by Acme (Changshu); Conductive coating :Baytron P, by HCStark (German ); HD-MB019, provided by the Beijing Jinhweili Applied Chemical Products Co., Ltd.;
Cymel 325,由氰特公司(上海)提供; D 604,由美國空氣化學(上海)提供; A-187,由邁圖新材料集團(上海)提供; NMP,試劑級; 二甲基乙醯胺,試劑級; 水,水離子水; 18 201026812 異丙醇,試劑級; 離型膜:SILFLU 50MD07,由 Siliconenature提供; SILFLU 75MD07W,由 Siliconenature提供。 2.製備方法 2.1配方 A.導電塗層的配方:Cymel 325, supplied by Cytec (Shanghai); D 604, supplied by American Air Chemistry (Shanghai); A-187, supplied by Momentive New Materials Group (Shanghai); NMP, reagent grade; dimethylacetamide , reagent grade; water, water ionized water; 18 201026812 isopropanol, reagent grade; release membrane: SILFLU 50MD07, supplied by Siliconenature; SILFLU 75MD07W, supplied by Siliconenature. 2. Preparation method 2.1 Formulation A. Formulation of conductive coating:
10 表9導電塗層配方(單位:克) Baytran P 6.600 50% DMAE 0.096 NMP 0.218 去離子水 5.000 異丙醇 5.000 HD-MD019 0.300 Cymel 325 0.080 正丁醇 0.250 A-187 0.003 D 604 0.008 固含量,% 1.04% 註:各原料依次加入,並邊攪拌邊慢慢加入; B.底塗配方: 表10矽氧烷底塗配方(單位:克) 丁酮 14.1 正庚烧 57.6 30% SS4191A 8 19 201026812 100% SS4191B 0.181 43% SS4192C 0.088 50% SS4259C 0.176 固含量, 3% c.膠配方 表1 1 7355矽氧烷黏合劑配方(單位:克)10 Table 9 conductive coating formula (unit: gram) Baytran P 6.600 50% DMAE 0.096 NMP 0.218 deionized water 5.000 isopropanol 5.000 HD-MD019 0.300 Cymel 325 0.080 n-butanol 0.250 A-187 0.003 D 604 0.008 solid content, % 1.04% Note: Each raw material is added in sequence and slowly added while stirring; B. Primer formulation: Table 10 Oxane basecoating formula (unit: gram) Butanone 14.1 Zhenggeng 57.6 30% SS4191A 8 19 201026812 100% SS4191B 0.181 43% SS4192C 0.088 50% SS4259C 0.176 Solids, 3% c. Glue Formulation Table 1 1 7355 Oxane Adhesive Formulation (Unit: gram)
7355 100 10% DCBPO 22.40 曱苯 30 共計: 152.40 固含量, 38% 5 表12 7406矽氧烷黏合劑配方(單位··克) 7406 100 10% A-75 22.40 甲苯 30 共計: 152.40 固含量, 38%7355 100 10% DCBPO 22.40 Benzene 30 Total: 152.40 Solids, 38% 5 Table 12 7406 Hydroxide Adhesive Formulations (Units·g) 7406 100 10% A-75 22.40 Toluene 30 Total: 152.40 Solids, 38 %
2.2製備過程 先在PI膜一側分別塗佈導電塗層、矽氧烷底塗、7406 矽氧烷黏合劑,工藝和塗佈厚度與例1相同;然後再在線複 10 合白色的氟素離型膜(SILFLU 50MD07W)。接著在PI的另 一側(另一側複合著離型膜)分別塗佈矽氧烷底塗和7355矽 20 201026812 氧烧黏合劑,石夕氧烧黏合劑厚度爲0.05mm。最後在線複合 SILFLU75MD07離型膜。 2.3性能 5 表13實例3的測試性能 性能 測試 測試方法 對鋼板的黏性:7355膠 面 0.40 N/mm ASTMD-3330 7406膠面 0.20 N/mm 拉伸強度 : 115 N/25mm ASTMD-882 斷裂伸長率: >40 % 膠帶總厚度: 0.105 mm ASTMD-3652 擊穿電壓: 6.5 Kv ASTMD-149 靜電耗散時間: <0.01 S 如前所述 産生靜電壓:自解卷 <100 V 如前所述 從FPC剝離 <100 V 如前所述,90 in/min的 解卷速度 财而溫 無殘膠、氣 泡 280°C lOmins 透明度 2 目視 實例4 1.原材料 21 201026812 基材:6051,25微米厚的聚醯亞胺膜,由天津市天緣電工 材料有限責任公司; 矽氧烷底塗:SS4191(SS4191A、SS4191B、SS4192C、 SS4259C)由邁圖新材料集團(上海)提供; 5 矽氧烷黏合劑:7355,由道康寧(上海)提供; 7406,由道康寧(上海)提供; A-75,阿克瑪(常熟)提供; 導電塗層:BaytronP,由 H.C.Stark(德國); 〇 HD-MB019, 水性聚丙烯酸,由北京金彙利應 10 用化工製品有限公司提供;2.2 Preparation process First, a conductive coating, a siloxane topcoat, and a 7406 decane adhesive were applied to the side of the PI film. The process and coating thickness were the same as in Example 1. Then, the white fluorination was repeated online. Type film (SILFLU 50MD07W). Next, on the other side of the PI (the other side is combined with the release film), a naphthenic base coat and a 7355 矽 20 201026812 oxy-fired adhesive are respectively applied, and the thickness of the shixi oxygen burning adhesive is 0.05 mm. Finally, the online composite SILFLU75MD07 release film. 2.3 Performance 5 Table 13 Test performance of Example 3 Performance test Test method Viscosity to steel plate: 7355 rubber surface 0.40 N/mm ASTMD-3330 7406 rubber surface 0.20 N/mm Tensile strength: 115 N/25mm ASTMD-882 elongation at break Rate: >40 % Total tape thickness: 0.105 mm ASTMD-3652 Breakdown voltage: 6.5 Kv ASTMD-149 Static dissipation time: <0.01 S Static voltage generated as described above: self-unwinding <100 V as before The stripping from FPC <100 V is as described above, the unwinding speed of 90 in/min is free of residual glue, the bubble is 280 ° C lOmins transparency 2 Visual Example 4 1. Raw material 21 201026812 Substrate: 6051, 25 Micron thick polyimide film, by Tianjin Tianyuan Electrical Material Co., Ltd.; 矽 底 底 :: SS4191 (SS4191A, SS4191B, SS4192C, SS4259C) provided by Momentive New Materials Group (Shanghai); 5 矽 oxygen Alkane binder: 7355, supplied by Dow Corning (Shanghai); 7406, supplied by Dow Corning (Shanghai); A-75, supplied by Acme (Changshu); Conductive coating: BaytronP, by HCStark (Germany); 〇HD- MB019, Waterborne Polyacrylic Acid, by Beijing Gold Huili Ying 10 is provided by Chemical Products Co., Ltd.;
Cymel 325,由氰特公司(上海)提供; D 604,由美國空氣化學(上海)提供; A-187,由邁圖新材料集團(上海)提供; NMP,試劑級; 15 二甲基乙醯胺,試劑級; 水,水離子水; φ 異丙醇,試劑級; 離型膜:SILFLU 50MD07,由 Siliconenature提供; SILFLU 75MD07W,由 Siliconenature提供。 20 2.製備方法 2.1配方 A.導電塗層的配方: 表14導電塗層配方(單位:克) 22 201026812Cymel 325, supplied by Cytec (Shanghai); D 604, supplied by American Air Chemistry (Shanghai); A-187, supplied by Momentive New Materials Group (Shanghai); NMP, reagent grade; 15 dimethylacetate Amine, reagent grade; water, water ionized water; φ isopropanol, reagent grade; release membrane: SILFLU 50MD07, supplied by Siliconenature; SILFLU 75MD07W, supplied by Siliconenature. 20 2. Preparation method 2.1 Formulation A. Formulation of conductive coating: Table 14 Conductive coating formula (unit: gram) 22 201026812
Baytran P 1.65 50% DMAE 0.096 NMP 0.218 去離子水 4.5 異丙醇 4.5 HD-MD019 0.570 Sancure 325 0.14 正丁醇 0.250 A187 0.003 D604 0.008 固含量,% 1.04% 註:各原料依次加入,並邊攪拌邊慢慢加入; B.底塗配方: 表15矽氧烷底塗配方(單位:克) 丁酮 14.1 正庚烧 57.6 30% SS4191A 8 100% SS4191B 0.181 43% SS4192C 0.088 50% SS4259C 0.176 固含量, 3% 5 C.膠配方 表161 7355矽氧烷黏合劑配方(單位:克) 23 201026812 7355 100 10% DCBPO 22.40 甲苯 30 共計: 152.40 固含量, 3 8% 表17 7406矽氧烷黏合劑配方(單位:克) 7406 100 10% A-75 22.40 甲苯 30 共計: 152.40 固含量, 38%Baytran P 1.65 50% DMAE 0.096 NMP 0.218 Deionized water 4.5 Isopropyl alcohol 4.5 HD-MD019 0.570 Sancure 325 0.14 n-butanol 0.250 A187 0.003 D604 0.008 Solids content, % 1.04% Note: The ingredients are added sequentially and stirred slowly. Slow addition; B. Primer formulation: Table 15 oxirane primer formulation (unit: gram) butanone 14.1 gamma burn 57.6 30% SS4191A 8 100% SS4191B 0.181 43% SS4192C 0.088 50% SS4259C 0.176 solid content, 3% 5 C. Glue Formulation Table 161 7355 Oxane Adhesive Formulation (Unit: gram) 23 201026812 7355 100 10% DCBPO 22.40 Toluene 30 Total: 152.40 Solid Content, 3 8% Table 17 7406 Oxane Adhesive Formulation (Unit: g) 7406 100 10% A-75 22.40 Toluene 30 Total: 152.40 Solids, 38%
2.2製備過程 5 先在PI膜一側分別塗佈導電塗層、矽氧烷底塗、7406 矽氧烧黏合劑,工藝和塗佈厚度與例1相同;然後再在線複 合白色的氟素離型膜(SILFLU 50MD07W)。接著在PI的另 一側分別塗佈導電塗層、矽氧烷底塗和7355矽氧烷黏合 劑,矽氧烷黏合劑層厚度爲〇.〇5mm。最後在線複合 1〇 SILFLU75MD07離型膜。 2.3性能 表1 8實例3的測試性能 |測試 |測試方法 24 201026812 對鋼板的黏性:7355膠 面 0.40 N/mm ASTMD-3330 7406膠面 0.20 N/mm 拉伸強度: 115 N/25mm ASTMD-882 斷裂伸長率: >40 % 膠帶總厚度: 0.105 mm ASTMD-3652 擊穿電壓: 6.5 Kv ASTMD-149 靜電耗散時間: <0.01 S 如前所述 産生靜電壓:從FPC剝離 <100 V 如前所述,90 in/min的 解卷速度 财1¾溫 無殘膠、氣 泡 280°C lOmins 透明度 2 目視 對比例1 1.原材料 基材:6051,25微米厚的聚醯亞胺膜,由天津市天緣電工 5 材料有限責任公司; 矽氧烷底塗:SS4191(SS4191A、SS4191B、SS4192C、 SS4259C)由邁圖新材料集團(上海)提供; 矽氡烷黏合劑:7355,由道康寧(上海)提供; A-75,阿克瑪(常熟)提供。 25 201026812 2.製備方法 2.1配方 A.底塗配方: 表19矽氧烷底塗配方 (單位:克) 丁酮 ΤΪΓΡ''" 正庚烷 rTe 30% SS4191A 8 — 100% SS4191B οΤΐΤΐ — 43% SS4192C 〇88 ~~~ 50% SS4259C~ 〇ΤΪ76 ~~~ 固含量, 3%^~ ^2.2 Preparation process 5 First, a conductive coating, a siloxane top coat, a 7406 矽 oxy-burn adhesive were applied to the side of the PI film, and the process and coating thickness were the same as in Example 1; then the white fluorinated release was repeated online. Membrane (SILFLU 50MD07W). Next, a conductive coating, a siloxane topcoat and a 7355 oxirane adhesive were applied to the other side of the PI, and the thickness of the siloxane adhesive layer was 〇.〇5 mm. Finally online compound 1〇 SILFLU75MD07 release film. 2.3 Performance Table 1 8 Test Performance of Example 3|Test|Test Method 24 201026812 Adhesion to Steel Plate: 7355 Rubber Surface 0.40 N/mm ASTMD-3330 7406 Rubber Surface 0.20 N/mm Tensile Strength: 115 N/25mm ASTMD- 882 Elongation at break: >40 % Total thickness of tape: 0.105 mm ASTMD-3652 Breakdown voltage: 6.5 Kv ASTMD-149 Static dissipative time: <0.01 S Static voltage generated as described above: Stripped from FPC <100 V As mentioned above, 90 in/min unwinding speed 13⁄4 temperature without residue, bubble 280 ° C lOmins transparency 2 visual comparison 1 1. Raw material substrate: 6051, 25 μm thick polyimide film, Tianjin Tianyuan Electric 5 Materials Co., Ltd.; 矽 底 底 primer: SS4191 (SS4191A, SS4191B, SS4192C, SS4259C) provided by Momentive New Materials Group (Shanghai); decane binder: 7355, by Dow Corning ( Shanghai) Provided; A-75, provided by Arkema (Changshu). 25 201026812 2. Preparation method 2.1 Formulation A. Primer formulation: Table 19: Oxygenane primer formulation (unit: gram) Butanone ΤΪΓΡ ''" n-heptane rTe 30% SS4191A 8 — 100% SS4191B οΤΐΤΐ — 43% SS4192C 〇88 ~~~ 50% SS4259C~ 〇ΤΪ76 ~~~ Solid content, 3%^~ ^
C.膠配方 表20矽氧烷黏合劑配方(單位:克) 7355 Ϊ00~~~--- 10% Α-75 2^40 甲苯 --------- 30 共計: 152.40 — 固含量, 3 8% 10 2·2製備過程 與例1相同,只是沒有塗佈導電層,僅塗矽氧烷底塗和 石夕氧烷黏合劑。 2·3性能 26 201026812 表21實例2的測試性能 性能 測試 測試方法 對鋼板的黏性:(等 待24h ,在23°C) 0.28 N/mm ASTMD-3330 鬃 拉伸強度 : 115 N/25mm ASTMD-882 斷裂伸長率: >40 % - 膠帶總厚度: 0.050 mm ASTMD-3652 擊穿電壓: 6,0 Kv ASTMD-149 靜電耗散時間: > 20S 如前所述 産生靜電壓:解卷過程 5,000-10,00 ον 如前所it, 90 in/min的解卷速度 :從FPC剝離 >5000V 如前所述, 90 in/min的解卷速度 对局溫 無殘膠、氣 泡 280〇C lOmins 透明度 2 目視 對比例2 根據EP422919實施例1揭露的方法製備的膠帶,並按 5 實例2的測試方法進行性能測試,透光度爲0或1。靜電釋放 時間小於0.01S。 耐溫條件:250攝氏度下最多只能保持5 秒鐘。 27 201026812 【圖式簡單說明】 圖1係根據本發明一個實施方式的結構示意圖。 【主要元件符號說明】 1基材 2導電塗層 3底塗 4膠層C. Glue Formulation Table 20 Oxygenane Binder Formulation (Unit: gram) 7355 Ϊ00~~~--- 10% Α-75 2^40 Toluene--------- 30 Total: 152.40 — Solid Content The preparation process of 3 8% 10 2·2 was the same as that of Example 1, except that no conductive layer was applied, and only the decane-based primer and the oxalate-based adhesive were applied. 2·3 performance 26 201026812 Table 21 Example 2 Test performance Performance test Test method Viscosity to steel plate: (waiting 24 h at 23 ° C) 0.28 N/mm ASTMD-3330 鬃 Tensile strength: 115 N/25 mm ASTMD- 882 Elongation at break: >40 % - Total thickness of tape: 0.050 mm ASTMD-3652 Breakdown voltage: 6,0 Kv ASTMD-149 Static dissipative time: > 20S Static voltage generated as described above: unwinding process 5,000 -10,00 ον As before, the unwinding speed of 90 in/min: stripping from FPC >5000V As mentioned above, the unwinding speed of 90 in/min has no residue on the local temperature, and the bubble is 280 〇C lOmins Transparency 2 Visually Comparative Example 2 An adhesive tape prepared according to the method disclosed in Example 1 of EP422919 was tested for performance according to the test method of Example 2, and the transmittance was 0 or 1. The electrostatic discharge time is less than 0.01S. Temperature resistance: up to 5 seconds at 250 degrees Celsius. 27 201026812 [Schematic Description of the Drawings] Fig. 1 is a schematic view showing the structure according to an embodiment of the present invention. [Main component symbol description] 1 substrate 2 conductive coating 3 primer 4 layer
2828
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| US20180093455A1 (en) * | 2015-03-31 | 2018-04-05 | Rogers Corporation | Substrates, laminates, and assemblies for flexible heaters, flexible heaters, and methods of manufacture |
| TWI691399B (en) * | 2015-03-31 | 2020-04-21 | 美商羅傑斯公司 | Substrates, laminates, and components for flexible heaters, flexible heaters, and methods of manufacturing the same |
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