TW201037053A - Double face adhesive tape - Google Patents

Double face adhesive tape Download PDF

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Publication number
TW201037053A
TW201037053A TW99107568A TW99107568A TW201037053A TW 201037053 A TW201037053 A TW 201037053A TW 99107568 A TW99107568 A TW 99107568A TW 99107568 A TW99107568 A TW 99107568A TW 201037053 A TW201037053 A TW 201037053A
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Taiwan
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adhesive tape
double
sided adhesive
thickness
mass
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TW99107568A
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Chinese (zh)
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TWI424042B (en
Inventor
Takeshi Iwasaki
Hiroki Takano
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Dainippon Ink & Chemicals
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Abstract

A double face adhesive tape, which is an adhesive tape that has adhesive agent layers on two faces of a foaming substrate. The interlayer strength of the foregoing foaming substrate is above 12N/cm. 25 percent compression strength is 30 to 170kPa. The foregoing adhesive agent layers are formed by acrylic based adhesive agent composition. The foregoing acrylic based adhesive agent composition contains: an acrylic based copolymer containing (methyl) acrylate having 4 to 12 carbon atoms and vinyl monomer having carboxyl as the monomer ingredients, and polymerized rosin ester based adhesiveness-providing resin. According to the double face adhesive tape, the excellent fitness, the reworking suitability, and re-peeling ability between the double face adhesive tape and the adhered body can be accomplished even if rigid bodies are laminated with each other, and furthermore immersion of water may be effectively avoided.

Description

201037053 六、發明說明: 【發明所屬之技術領域】 發月係關於以發泡體基材為中芯的雙面黏著帶 【先前技術】201037053 VI. Description of the invention: [Technical field to which the invention pertains] A double-sided adhesive tape with a foam base material as a center core [Prior Art]

在電子筆記本、手機、PHS、照相機、音樂播放器、電 視等可攜式電子機器中,以資訊顯示部的保護面板與殼體 的貼合為代表’在各種構件、模組的固定方面使用雙面黏 著帶。為了確保在市場中的競爭優越性,而追求著多種多 樣的功能,其中之-,追求著賦予防水性功能。 作為用於電子機器的構件的固定用㈣著帶,已公開 如下技術:例如,在-40〜-i5t的溫度範圍具有損耗正切“扣 5)的極大值、對於特定的被黏體的面黏接強度為i9N/ 以上的黏著劑層設置於支撐體的兩面的雙面黏著薄片(參考 專利文獻1)。該雙面黏著薄片,藉由具有特定的黏著劑層, 因而具有良好的黏接力,具有不易發生因物體的落下時的 衝擊所導致的構件的脫落這樣的優異的耐衝擊性。但日, 如保護面板和殼體的黏接、殼體和殼體的黏接,在剛體彼 此的接合中’就該雙面黏著薄片而言,由於在與被黏體的 接合面上難以獲得完全的密合,有時有微小的空隙時就會 發生浸水的情況。 作為密合性優異的雙面黏接膠帶,已公開了如下雙面 黏接膠帶,其以發泡體為基材、具有:顯示損耗正切“抓占) 的極大值的溫度為-251以下、在〇°C的保持試驗中的保持 時間為24小時以上的丙烯酸系黏著劑層(參考專利文獻 3 201037053 2)。就該雙面黏接膠帶而言,對 在構件彼此的黏接時,士 、掛曰為優異,即使 僅… 將構件間適宜地接合,是, 早獨地將發泡體用作基 μ m n〜 们居便難以在構件和黏接劑 層的界面能夠抑制至微小的 Λ Λ, ^ 即使该界面的一部分上 啕j被水次入的空隙或浮起, 入路,因而難以眚银吐Ρ 由於曰從那裡擴大水的侵 吨難以實現防水性。縣&丨β + -r·… 途中,# 特另〗疋在可攜式電子機器用 薄枣m七 •輯件隨的狹框架化、進-步的 溥i化的要求,在追求著 的m⑽ 錢乍的膠页見度、薄的膠帶厚度 的障况下’難以賦予充分的防水性。 =就可攜式電子機器等而言’為了提高製造時的 構㈣ 未成功地接合於未完成品的雙面黏著帶、 構件專進行剝離(再加工),有時 负矸會為了將元成品進行修理或 生、再利用而將殼體、構件進杆八 進仃刀離•分解•解體,但 牙、以在的發泡體基材的替面點輩渔二 w旳又面黏者帶而言,由於發泡體基材 谷易發生層間損壞’容易殘留於構件表面,且去除困難, ^此降低了從殼體、構件去除雙面黏著帶之後重新貼合新 、雙面黏著帶的作業的效率’殼體、構件、製品的良率, 以及回收率。 但是,就以往的發泡體基材而言,雖然追求著在厚度 方向壓縮時的軟度(壓縮強度),但沒有對於在厚度方向拉伸 :it況下的強度(層間強度)的概念。另外,單獨地降低黏著 劑的黏接力的情況下’由於與被黏體的密合性也降低,因 而難以賦予充分的防水性。 專利文獻1 :特開2〇〇5-1875 13號公報 專利文獻2 :特開2005-281360號公報 201037053 【發明内容】 發明所欲解決之課題 本發明要解決的課題在於提供 被黏體的黏接性、跟隨性良好,雙:黏耆帶’其與 和再剝離性優異。 纟且再加工一k)適合性 另外’除了上述課題以外,、罗担# 直且右得里沾, 還如供一種雙面黏著帶, ❹ _ 疋適用於電子機器用途的防水用 的雙面黏著帶。 用 進一步’除了上述課題以外 _ ^ ^ ^ 〜π λ冲,還挺供一種雙面黏著帶,In a portable electronic device such as an electronic notebook, a mobile phone, a PHS, a camera, a music player, a television, etc., the bonding of the protective panel and the housing of the information display unit is represented by the use of double in the fixing of various components and modules. Adhesive tape. In order to ensure the superiority of the competition in the market, and to pursue a variety of functions, among them, the pursuit of water resistance. As a fixing (four) belt for a member for an electronic machine, the following technique has been disclosed: for example, a maximum value of loss tangent " buckle 5" in a temperature range of -40 to -5 Torr, and a surface sticking to a specific adherend a double-sided adhesive sheet having adhesive layers having a strength of i9N/above provided on both sides of the support (refer to Patent Document 1). The double-sided adhesive sheet has a good adhesive force by having a specific adhesive layer. It has excellent impact resistance such that the member is not easily peeled off due to an impact when the object is dropped. However, for example, the adhesion of the protective panel and the casing, and the adhesion of the casing and the casing are in the rigid bodies. In the case of the double-sided adhesive sheet, it is difficult to obtain complete adhesion on the joint surface with the adherend, and water may be immersed when there are minute voids. For the surface-adhesive tape, the following double-sided adhesive tape has been disclosed, which has a foam as a base material and has a temperature at which the maximum value of the loss tangent "grab" is -251 or less, and the holding test at 〇 ° C Keep in For 24 hours or more between the acrylic adhesive layer (refer to Patent Document 32010370532). In the double-sided adhesive tape, when the members are bonded to each other, the shackles and the shackles are excellent, and even if only the components are properly joined, the foam is used as the base mn. ~ It is difficult for them to suppress the microscopic flaws at the interface between the member and the adhesive layer. ^ Even if a part of the interface is filled with water or a floating space, it is difficult to smash silver. It is difficult to achieve water repellency because of the expansion of water from the cockroaches. County & 丨β + -r·... On the way, #特别〗 In the pursuit of the narrow frame of the portable electronic machine, the requirements of the narrow frame, the advancement of the step, the pursuit It is difficult to give sufficient waterproofness under the barrier of the thickness of the rubber sheet of the m(10). = In the case of a portable electronic device, etc., in order to improve the structure at the time of manufacture (4), the double-sided adhesive tape which is unsuccessfully bonded to the unfinished product, and the component are separately peeled (reprocessed), and sometimes the defective product is used for the finished product. Repairing, raw, and reusing, the shell and the member are put into the rod and the knives are separated and decomposed and disintegrated, but the teeth and the foam substrate are replaced by a pair of fish. In this case, since the foam substrate is prone to interlayer damage, it is easy to remain on the surface of the member, and the removal is difficult, thereby reducing the reattachment of the new double-sided adhesive tape after removing the double-sided adhesive tape from the casing and the member. The efficiency of the job 'shell, component, product yield, and recovery rate. However, in the conventional foam substrate, although the softness (compressive strength) at the time of compression in the thickness direction is pursued, there is no concept of strength (interlayer strength) in the case of stretching in the thickness direction. Further, when the adhesive strength of the adhesive is lowered individually, the adhesion to the adherend is also lowered, so that it is difficult to impart sufficient water repellency. [Problem to be Solved by the Invention] The problem to be solved by the present invention is to provide a sticky body of a adherend. Good adhesion and followability, double: adhesive tape 'excellent and re-peelability.再 and re-processing one k) suitability in addition to the above-mentioned topics, Luo Dan # straight and right-handed, as for a double-sided adhesive tape, ❹ _ Adhesive tape. Further ‘ _ ^ ^ ~ λ λ, in addition to the above-mentioned subject, is quite suitable for a double-sided adhesive tape.

其具有優異的耐"整Wm iU 丁衡擎性,疋適用於可攜式電子機器用途的 防水用的雙面黏著帶。 用以解決課題之手段 本發明人進行了深入研究,結果發現了:藉由使用呈 有特定的柔軟性和制強度的發泡體基材來作為基材以^ 配合了特疋的組成的黏著劑,即使在剛體彼此的貼合時, 也可實現雙面黏著帶與被黏體之間的€異的密合性和再加 工適合性、再剝離性,進而可有效地防止水的浸潰,從而 解決了上述課題。 即本發明提供一種雙面黏著帶,係在發泡體基材的兩 面上具有黏著劑層的雙面黏著帶,其特徵在於,上述發泡 體基材的層間強度為12N/ cm以上,25%壓縮強度為30〜 170kPa ’該黏著劑層係由丙烯酸系黏著劑組合物所構成, 該丙烯酸系黏著劑組合物係含有丙烯酸系共聚物與聚合松 香醋(rosin ester)系黏著賦予樹脂,該丙烯酸系共聚物係含 5 201037053 有=原子數為4〜12的(甲基)丙稀酸s旨和具有緩基的乙烤 基單體作為單體成分。 發明效果 本發明的雙面黏著帶,由於不易發生發泡體基材的層 間損壞’另外即使在產生了層間裂痕的情况下,黏著劑也 :會殘留於構件表面而容易剝離’因&,在可攜式電子機 益等的製造時,將未成功地接合於未完成品的雙面黏著帶 構件等進行剝離(再加工)的情况下,以及在為了對可攜式電 子機器等完成品進行修理或再生、再利用而將殼體、構件 進行分離•分解•解體的情况下,可改善從殼體、構件去 除雙面黏㈣之後重新貼合新的冑面黏t帶的力業的效率 殼體、構件、製品的良率以及回收率。 進步,本發明的雙面黏著帶顯示出與被黏體的適宜 的密合性’可有效地防止水從密合間隙的浸入,具有優異 的防尺力此因此,對於薄型化提高、殼體内的容積限制 嚴格,對於難以另行設置水密封手段的可攜式電子機器等 而言’也可有效地賦予防水功能。 【實施方式】 本發明為一種雙面黏著帶,其在發泡體基材的兩面上 具有黏著劑層的雙面黏著帶,其特徵在於,前述發泡體基 材的層間強度為12N/cm以上,25%壓縮強度為3〇〜 1 70kPa,該黏著劑層係由丙烯酸系黏著劑組合物所構成, 3亥丙烯酸系黏著劑組合物係含有丙烯酸系共聚物與聚合松 香酯系黏著賦予樹脂,該丙烯酸系共聚物係含有碳原子數 6 201037053 為4〜12的(甲基)丙烯酸酯和具有羧基的乙烯基單體作 皁體成分。 〔發泡體基材〕 本發明使用的發泡體基材為:層間強度為12N/Cm以 上,較佳為15〜40N/cm,更佳為18〜35N/cm的發泡體 基材。藉由使用層間強度為該範圍的發泡體,即使在柔軟 的發泡體基材產生了基材的層間裂痕的情況下,也可賦^ 雙面黏著帶的易剝離性。 在此,就層間強度而言,首先在要評價層間強度的發 泡體的兩面,貼合各i張厚度為5〇/zm的強黏著性的黏著 劑層之後,在4(TC熟化48小時,製成層間強度測定用的雙 面黏著帶。 接著,在23。(: · 50% RH的環境下,用2kg的輥,在不 錄鋼板(表面用# 360號的耐水研磨紙進行了極細線紋化 (hairline)處理)上,將在一側的黏著面上内襯有厚度為25 # m的聚酯膜的2cm寬、10cm長(聚烯烴系發泡體的流動方向) 的雙面黏著帶試樣進行1個來回的加壓貼附,在4 〇放置 48小時。在23 °C放置24小時後,測定在23 °C · 50% RH的 環境下’以300mm/min的拉伸速度,在90度方向上將發 泡體撕裂時的強度。 本發明使用的發泡體基材為:25%壓縮強度為3〇〜 170kPa ’較佳為40〜150kPa的發泡體基材。藉由使用25 %壓縮強度為該範圍的發泡體基材,具有與被黏體的優異 的密合性’特別地對於具有凹凸形狀、粗糙面的被黏體, 也適宜地跟隨而具有優異的密合性。另外,就該壓縮強度 7 201037053 的發/包體基材而言,由於具有適度的緩衝性,貼附時的壓 力便集中於接合部,從而容易擠出存在於黏接介面的空 氣,因此在剛體彼此的接合方面,也可實現不產生水進入 的空隙之優異的密合性。 ^在此,就25%壓縮強度而言’將切斷成50mm見方的 试樣疊合至厚度為,約1Gmm。用面積大於試樣的板央住試 樣,在23t下以10mm/min的速度將試樣壓縮為約 2.5mm(原厚度的25%量),然後停止,測定經過2()秒後的 強度。 。就本發明使用的發泡體基材而言包體基材的拉伸 彈性模數為200N/em2以上。單位寬度的拉伸強度為i〇n /cm以上,較佳為12 5N/cm以上,更佳為以上。 另卜士刀斷伸長率雖然沒有特別限定,但$⑽〜1 〇〇〇% , 較佳為300〜700%。藉由使用拉伸彈性模數、拉伸強度、 切斷伸長率為該範圍的發泡體基材,即使為發泡了的季軟 的基材’也可抑制雙面黏著帶的加工性的惡化、破碎,貼 附作業性的降低。另外,在剝離雙面黏著帶時,難以產生 發泡體的層間損壞’即使在產生了層間裂痕的情況下,也 可軾予雙面黏著帶的易剝離性。 ^此,前述的拉伸彈性模數、單位寬度的拉伸强度為: 吏yensil〇n拉伸試驗機,在23t · 5繼h的還境下,在 =Γ3°〇_〜測定條件下,對標線長度峰 m , 又1 cni的樣品進行測定而獲得的 瑕大强度。 藉由使本發明所使用 的發泡體基材的發泡結構為獨立 201037053 :㈣構’由於可有效地防止來自發泡體基材的切斷面的 -水,故較佳。形成獨立氣泡結構的氣泡形狀雖然沒有特 =定i但是’相比於發泡體的厚度方向的平 而吕,流動方向、寬度方向、或這兩個方向的平均氣泡直 ::較長的形狀的獨立氣泡’由於具有適度的緩衝性,故較 Ο Ο 發泡體基材的發泡倍率雖然沒有特別限定 將層間強度、壓縮強度等調整為上述範者谷 ,、被黏體的優異的进合性和剝離容易度的方面考 〜12倍,較佳為2〜8倍,更佳為2 4〜5倍。.。马 取基材的厚度方向的平均氣泡直徑而言,雖秋 決於發泡體的厚度,但適宜為心,較佳為5〜㈣ =公為10〜100"m。發泡體基材的流動方 产 方向的平均氣泡直徑較佳為…。。一 二,最佳為1。〇〜·m。藉由使平均氣泡直徑為該: 即使在雙面黏著帶的寬度變得狹窄的情況下,也容易 路徑蜀立氣泡’可適宜地遮斷來自發泡體基材斷面的浸水 平均氣泡直徑的比率雖然沒有特別限定,但 的2動方向的平均氣泡直徑相對於發泡二 =均氣泡直徑的比(流動方向的平均氣泡直 °的平均氣泡直徑)較佳為J 2〜15,更又 發泡體基材的寬度方向 另外, 的厚声方“工A 相對於發泡體基材 的平均氣泡直徑的比(寬度方向的平均: 旱度方向的平均氣泡直徑)較佳為1>2〜15,更佳為2〜 9 201037053 11。另外,最佳為流動 當該比率為1.2以上時,° ^度方向皆為上述比率範圍。 因此提高了跟隨性。另彳2易確保厚度方向的柔軟性, 泡體基材的流動方向和办為15彳°以下時,不易發生發 均勻現象。 X方向的柔軟性或拉伸強度的不 ^ ^ ,'、 平均氣泡直徑的比率較;:、’现動方向和寬度方向的 倍。當為上述比率範圍時 :。’更佳為〇·33〜3 向和寬度方向的学軟性 χ生發泡體基材的流動方 發泡體基材的宽侉士二 ’勺現象。 流動方向都切斷為lcm。接著 Α在見度方向、 所切斷的發泡體基材的切斷面中二::顯微鏡(_)將 發泡體基材的寬度方向或0倍之後’對 J A机動方向的斷面 泡體基材的切斷面在該基材 ’、、、 " 納於照片巾。在所獲得的辟 -上都被谷 測疋出流動方向或寬戶 方向的放大前的實際長度為2mm ^寬度 入如认# .办士 " 丨刀的切斷面申所存在的 王_泡直徑,根據其平均值來算出平均氣泡直徑。 =體基㈣厚度方向的平均氣泡直徑, 要領來測定。首先,測定由SEM 乳的 運仃拍-的發泡體基材的 厚度。接者,與發泡體基材的流動方向的平均氣泡直徑測 定相同的條件下進行SEM拍照。接著,在所獲得的照片中, 藉由目視來計數出發泡體基材的任意的部位所存在的厚度 方向的氣泡數,藉由以下式子來算出厚度方向的平均氣泡 直徑。 10 201037053 厚度方向的平均氣泡直徑U m)=發泡體基材的厚度 (//m)/氣泡的個數 又 在任意的3部位對其進行測定,將其平均值作為厚度 方向的平均氣泡直徑。 &It has excellent resistance to "Wm iU" and is suitable for waterproof double-sided adhesive tapes for portable electronic applications. The inventors of the present invention conducted intensive studies and found that by using a foam substrate having a specific flexibility and strength as a substrate, the adhesion of the composition of the composition is matched. Even when the rigid bodies are bonded to each other, the adhesion between the double-sided adhesive tape and the adherend, the reworkability and the re-peelability can be achieved, and the water can be effectively prevented from collapsing. Thus, the above problems are solved. That is, the present invention provides a double-sided adhesive tape which is a double-sided adhesive tape having an adhesive layer on both sides of a foam base material, wherein the foam base material has an interlayer strength of 12 N/cm or more, 25 The % compressive strength is 30 to 170 kPa. The adhesive layer is composed of an acrylic pressure-sensitive adhesive composition containing an acrylic copolymer and a rosin ester-based adhesion-imparting resin. The acrylic copolymer contains 5 201037053 = (meth)acrylic acid having an atomic number of 4 to 12 and an ethyl bake monomer having a slow group as a monomer component. Advantageous Effects of Invention The double-sided adhesive tape of the present invention is less likely to cause interlayer damage of the foam base material. Further, even in the case where interlayer cracks occur, the adhesive agent may remain on the surface of the member and be easily peeled off due to & In the case of manufacturing a portable electronic device, etc., when a double-sided adhesive tape member or the like that has not been successfully bonded to an unfinished product is peeled off (reprocessed), and in order to be finished for a portable electronic device or the like When the shell or the member is separated, disassembled, or disassembled by repair, regeneration, and reuse, it is possible to improve the force of removing the double-sided adhesive (4) from the casing and the member and then reattaching the new surface-bonded t-belt. Efficiency shell, component, product yield and recovery. Advance, the double-sided adhesive tape of the present invention exhibits a suitable adhesiveness with the adherend', which can effectively prevent the intrusion of water from the adhesion gap, and has an excellent resistance to the ruler. Therefore, for thinning, the casing is improved. The internal volume limitation is strict, and it is also effective for providing a waterproof function for a portable electronic device or the like which is difficult to provide a water sealing means. [Embodiment] The present invention relates to a double-sided adhesive tape having a double-sided adhesive tape having adhesive layers on both sides of a foam substrate, wherein the foam substrate has an interlayer strength of 12 N/cm. The above 25% compressive strength is 3 〇 to 1 70 kPa, and the adhesive layer is composed of an acrylic pressure-sensitive adhesive composition, and the acrylic adhesive composition contains an acrylic copolymer and a polymerized rosin ester-based adhesion-imparting resin. The acrylic copolymer contains a (meth) acrylate having a carbon number of 6 201037053 of 4 to 12 and a vinyl monomer having a carboxyl group as a soap component. [Foam substrate] The foam substrate used in the present invention is a foam substrate having an interlayer strength of 12 N/cm or more, preferably 15 to 40 N/cm, more preferably 18 to 35 N/cm. By using a foam having an interlayer strength within this range, the peeling property of the double-sided adhesive tape can be imparted even when an interlayer crack of the substrate occurs in the flexible foam substrate. Here, in terms of the interlayer strength, first, each of the two adhesive layers having a thickness of 5 Å/zm is bonded to both sides of the foam to which the interlayer strength is to be evaluated, and then 4 (TC is cured for 48 hours). A double-sided adhesive tape for measuring the strength of the interlayer is produced. Next, in a 23: (: 50% RH environment, a 2 kg roller is used, and the steel sheet is not recorded (the surface is made of #360 water-resistant abrasive paper) On the one side of the hairline treatment, the adhesive surface of one side is lined with a 2 cm wide and 10 cm long (flow direction of the polyolefin-based foam) of a polyester film having a thickness of 25 # m. The adhesive tape sample was subjected to one back and forth pressure attachment, and placed at 4 48 for 48 hours. After standing at 23 ° C for 24 hours, it was measured to stretch at 300 mm/min in an environment of 23 ° C · 50% RH. Velocity, strength when the foam is torn in the direction of 90 degrees. The foam substrate used in the present invention is a foam substrate having a 25% compression strength of 3 Torr to 170 kPa, preferably 40 to 150 kPa. By using a 25% foam strength base material in this range, it has excellent adhesion to the adherend', especially for having The adherend of the convex shape and the rough surface is also suitably followed to have excellent adhesion. In addition, as for the hair/envelope substrate of the compressive strength 7 201037053, since it has moderate cushioning properties, when attached The pressure is concentrated on the joint portion, so that it is easy to extrude the air existing in the bonding interface, so that excellent adhesion of the gap in which water does not enter can be achieved in terms of joining the rigid bodies. In terms of % compressive strength, the sample cut into 50 mm square is laminated to a thickness of about 1 Gmm. The sample is compressed by a plate having a larger area than the sample, and the sample is compressed at a speed of 10 mm/min at 23 t. About 2.5 mm (25% of the original thickness), and then stopped, and measured the strength after 2 () seconds. The tensile elastic modulus of the inclusion substrate was 200 N for the foam substrate used in the present invention. /em2 or more. The tensile strength per unit width is i〇n /cm or more, preferably 12 5 N/cm or more, more preferably more. The elongation of the knife is not particularly limited, but $(10)~1 〇 〇〇%, preferably 300 to 700%, by using tensile modulus, tensile strength, In the foam base material having the elongation at break in this range, even in the case of the foamed soft base material, the deterioration of the workability of the double-sided adhesive tape and the breakage can be suppressed, and the workability of the attachment can be lowered. When the double-sided adhesive tape is peeled off, it is difficult to cause interlayer damage of the foam. Even in the case where interlayer cracks are generated, the peeling property of the double-sided adhesive tape can be imparted. Thus, the aforementioned tensile elastic modulus, The tensile strength per unit width is: 吏yensil〇n tensile testing machine, under the condition of 23t · 5 followed by h, under the condition of =Γ3°〇_~, the length of the marking line is m, and 1 cni The strength of the sample obtained by the measurement of the sample. The foamed structure of the foam base material used in the present invention is preferably 201037053: (4) The structure is effective because it can effectively prevent water from the cut surface of the foam substrate. The shape of the bubble forming the closed cell structure is not as specific as that of the thickness direction of the foam, and the average direction of the flow direction, the width direction, or both directions is straight:: a long shape Since the independent bubble "has a moderate cushioning property, the expansion ratio of the foam substrate is not particularly limited, and the interlayer strength, the compressive strength, and the like are adjusted to the above-described range, and the adherend is excellent. The aspect of the compatibility and the ease of peeling is ~12 times, preferably 2 to 8 times, more preferably 2 4 to 5 times. . . . The average cell diameter in the thickness direction of the substrate is preferably a heart, although it depends on the thickness of the foam, preferably 5 to (4) = 10 to 100 " m. The average bubble diameter in the flow direction of the foam substrate is preferably... . One or two, the best is 1. 〇~·m. By making the average bubble diameter as follows: even in the case where the width of the double-sided adhesive tape becomes narrow, it is easy to block the standing bubble" to appropriately block the average bubble diameter of the water immersion from the cross section of the foam substrate. Although the ratio is not particularly limited, the ratio of the average bubble diameter in the two moving directions to the bubble diameter = the average bubble diameter (the average bubble diameter in the flow direction) is preferably J 2 to 15, and is more complicated. In the width direction of the bubble base material, the ratio of the thick sound side "average A to the average bubble diameter of the foam base material (average in the width direction: average bubble diameter in the dry direction) is preferably 1 > 2~ 15, more preferably 2 to 9 201037053 11. In addition, the optimum flow is when the ratio is 1.2 or more, and the ° ^ direction is the above ratio range. Therefore, the followability is improved. Sexuality, when the flow direction of the foam substrate is less than 15 彳, it is not easy to cause uniformity. The softness or tensile strength of the X direction is not ^^, ', and the average bubble diameter ratio is compared; Current direction and width When it is the above ratio range: 'Better than the width of the 〇·33~3 direction and the width direction of the soft side of the foamed base material of the flow side foam substrate of the wide gentleman's scoop phenomenon. The flow direction is cut to 1 cm. Then, in the direction of the visibility, the cut surface of the cut foam substrate is two:: the microscope (_) will be in the width direction of the foam substrate or after 0 times' The cut surface of the cross-section bubble substrate of the JA maneuvering direction is on the substrate ',, " in the photo towel. On the obtained basis, the flow direction or the direction of the wide household is measured by the valley. The actual length before the enlargement is 2mm ^ Width into the # 认 . 办 & & & & 切断 切断 切断 切断 切断 切断 切断 申 申 王 王 王 王 王 王 王 王 王 王 王 = = = = = = = = = = = = = = = = = = The average bubble diameter is measured by the method. First, the thickness of the foam base material by the SEM emulsion is measured. The contact is performed under the same conditions as the average bubble diameter measurement in the flow direction of the foam substrate. SEM photographing. Next, in the obtained photograph, the foam was counted by visual inspection. The number of bubbles in the thickness direction existing in any part of the material is calculated by the following formula. The average bubble diameter in the thickness direction is calculated by the following formula: 10 201037053 Average bubble diameter U m in the thickness direction = thickness of the foam substrate (// The number of m)/bubbles is measured in any three places, and the average value is taken as the average bubble diameter in the thickness direction.

^發泡體基材的層間強度、壓縮強度和拉伸彈性模數 等,可藉由所使用的基材的原材料、發泡結構來適宜調整。 本發明使制發泡體基材的種類,只要為具有上述層間強 度、壓縮強度,拉伸彈性模數等的發泡體基材,就不受特 別限制’可使用由聚乙烯、聚丙烯、乙烯-丙烯共聚物、乙 烯-乙酸乙烯酯共聚物等構成的聚烯烴系發泡體,聚胺酯系 發泡體,自丙烯酸系橡膠、其他的彈性體等構成的橡:系 發泡體等,其[由於容易製備出對被黏體表面的凹凸的 跟隨性、緩衝吸收性等優異的薄的獨立氣泡結構的發泡體 基材,因此可較佳使用聚烯烴系發泡體。 發泡體基材的厚度雖然只I根據使㈣態來適宜調整 即可,為5(^20(^ m。在電子機器的構件的固定用的情= 下’特別是在小型、薄型的可攜式電子機器的情況下:由 於追求著薄的膠帶厚度,因此基材厚度較佳$ 5〇〜_ m,更佳為70〜400"m。 ,叫π丨,设付的交聯 烯煙系樹月旨發泡體:將„烴系樹脂和熱分解型發 供給於擠出機進行㈣混煉,從擠出機擠出成為片狀 成L包性?㈣烴系樹脂薄片,使用電子射線對其進行交: 之後’進行發'泡、延展、薄片化’從而獲得。關: 系樹脂’可使用以往公知的聚稀煙系樹脂,但較佳為心 11 201037053 40質量%以上藉由使用包含四價過渡金屬的 J i屬方香類化 合物而獲得的聚乙烯系樹脂的聚烯烴系樹脂。另外,也^ 通過在使該發泡體發泡後,將該發泡薄片在厘由 %坪復方向切片 後’用熱輥進行延展、結皮,從而製造。 在發泡體基材中,根據需要可向樹脂中任意地添加如 下公知的添加劑:可塑劑’軟化劑,抗氧化劑,阻燃劑, 玻璃、塑料製的纖維•空心微球(ball〇on) ·珠.金屬粉末等 填充劑,顏料•染料等著色劑,調平劑,增黏劑,拒水劑, 消泡劑等。 就發泡體基材而言,為了提高與黏著劑層或其它層的 密合性,也可進行電暈處理、火焰處理、等離子體處二、 熱風處理、臭氧•紫外線處理、易黏接處理劑的塗布等表 面處理。就表面處理而言,藉由使基於潤濕試劑的潤濕指 數為36mN/m以上,較佳為4〇mN//m以上,進一步較佳 為48mN/m以上,可獲得與黏著劑的良好的密合性。 〔黏著劑層〕 構成本發明的雙面黏著帶的黏著劑層的黏著劑組合物 =特徵在於’由丙烯酸系黏著劑組合物所構成,所述丙稀 酸系黏著劑組合物含有丙烯酸系共聚物與聚合松香醋系黏 著賦予樹脂’肖丙烯酸系共聚物係含有碳原子數為4〜12 的(甲基)丙埽酸6旨和具有叛基的乙烯基單體作為單體成分。 作為蚊原子數為4〜12的(甲基)丙締酸酯,可列舉出: ' (甲基)丙烯酸甲酯、(甲基)丙烯酸乙酯、(甲基)丙烯 酸正丁酯、(甲基)丙烯酸異丁酯、(甲基)丙烯酸叔丁酯、(甲 土)丙烯酸正辛酯、(甲基)丙烯酸異辛酯、(甲基)丙烯酸異壬 12 201037053 酯、(曱基)丙烯酸環己酯、(曱基)丙烯酸2-乙基己酯等單體, 可使用它們的1種或2種以上。其中,烷基的碳原子數為4 〜8的(甲基)丙烯酸酯,特別是丙烯酸正丁酯,由於容易確 保與被黏體的密合性’並且凝聚力、對皮脂類的耐受性優 異,故較佳。丙烯酸正丁酯的含量較佳為全部的碳原子數 為4〜12的(甲基)丙烯酸酯中占60質量%以上,更佳為占 90質量%以上。 丙烯酸系共聚物中的(甲基)丙烯酸酯的含量較佳為構 成丙烯酸系共聚物的單體成分中占8〇〜985質量%,更佳 為90〜98.5質量%。 作為具有羧基的乙烯基單體,可使用丙烯酸、甲基丙 烯酸、衣康酸、馬來酸、(甲基)丙烯酸二聚物、巴豆酸、環 氧乙烷改性琥站酸丙烯酸醋等,其中較佳為將丙烯酸用作 共聚合成分。 丙烯酸系共聚物中的具有羧基的乙烯基單體的含量較 〇 佳為構成丙烯酸系共聚物的單體成分中的〇5〜1〇〇質量 %,更佳為1.5〜5.0質量%。 進一步,就構成本發明的雙面黏著帶的黏著劑層的黏 著劑組合物所使用的丙烯酸系共聚物而言,較佳 分子内具有3級胺骨架的乙烯基單體作為單體成;,理由 在於:可使凝聚力優異並且可抑制黏接力過度提高,因而 對於作為電子機器的殼體、構件等材料的聚苯乙烯、㈣、 丙烯酸類、聚碳酸酉旨、聚酿胺聚§旨、聚丙婦、聚Μ 1 樹脂等樹脂,残鋼、铭、鑛鋅鋼板等金屬,破璃等而古, 可兼顧良好的密合性和再加工適合性、以及再剥離性。 201037053 作為分子内具有3級胺骨架的乙烯基單體,可使用N 乙烯基吡咯烷酮、N-乙烯基己内醯胺、丙烯醯基嗎啉、n,n 二甲基丙烯醯胺等等,其中較佳為將N_乙烯基吡咯烷酮用 作共聚合成分。 丙烯酸系共聚物中的分子内具有3級胺骨架的乙烯基 單體的含量較佳為構成丙烯酸系共聚物的單體成分中的〇5 〜5.0質量% ’更佳為15〜3_0質量%。 另外,將異氰酸醋系交聯劑用作本發明使用的丙烯酸 系共聚物的交聯劑的情況下,作為具有與其反應的官能團 的乙烯基單體,較佳為使用含羥基的乙烯基單體。 作為具有經基的乙稀基單體,可使用例如,(曱基)丙 稀酸24基乙S旨、(甲基)丙稀酸2_經基丙醋、(甲基)丙稀 -夂L基丁 S日(甲基)丙稀酸6•經基己醋等的含經基的(甲 基)丙稀酸醋,其中特佳為(甲基)丙稀酸2-經基乙酿、(甲 基)丙稀酸4,基丁醋。與異氛酸醋系交聯劑反應的含經基 的=稀基早體的含量較佳為構成_酸系共聚物的單體成 ^ ^ %,特別較佳為0.03〜〇·3質量%。 作為7的乙烯基單體,可舉出:乙酸乙_、2_丙稀 酿胺-2 -曱基丙確酸等今泣^ -. t 尹'欠基早體;碳原子數為1〜3的(甲 基)丙烯酸酯、碳原子數為 基㈣酸異冰片,、笨為二上:(甲基㈣酸酿、(甲 其他的乙缚基單艘二::的乙烯基單想。 的單體成分中的i 5〜2 0』旦里又仏為構成丙稀酸系共聚物 進-步較佳為2〜8質量J 更佳為1·5〜1"*%’ 黏著劑的凝聚力 '保拉/。藉由含有於該範圍’可容易將 、力、黏接性調整為適宜的範圍。 14 201037053 丙烯酸系共聚物可藉由溶液聚合法 浮聚合法、乳液聚合法等公知的聚合方法來!;Γ懸 付,但從黏著劑的耐水性考慮,較佳為溶液聚合法二獲 聚合法°,合㈣發方法也可任意地選擇如下;法:使^ 了過氧化本甲冑、過氧化月桂醯等過氧化物系 丁腈等偶氣系的熱聚合起始劑的熱引發方法;㈣= _糸、苯偶姻喊李、贫技# 加么 / 本偶醯縮酮系、醯基氧化膦系、苯偶The interlayer strength, compressive strength, tensile modulus and the like of the foam base material can be suitably adjusted by the raw material of the substrate to be used and the foam structure. The type of the foam base material to be used in the present invention is not particularly limited as long as it is a foam base material having the above-mentioned interlayer strength, compressive strength, tensile modulus, and the like, and polyethylene, polypropylene, and the like can be used. a polyolefin-based foam composed of an ethylene-propylene copolymer, an ethylene-vinyl acetate copolymer, a polyurethane foam, an oak-based foam composed of an acrylic rubber or another elastomer, and the like. [The foam base material having a thin closed cell structure excellent in adherence to irregularities on the surface of the adherend, buffer absorption, and the like is easily produced. Therefore, a polyolefin-based foam can be preferably used. The thickness of the foam base material may be appropriately adjusted according to the (four) state, and may be 5 (^20 (^m. in the case of fixing the member of the electronic device = lower), particularly in a small, thin type. In the case of portable electronic devices: due to the pursuit of a thin tape thickness, the thickness of the substrate is preferably $5〇~_m, more preferably 70~400"m., called π丨, the crosslinked olefin smoke系 月 旨 : : : 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃 烃The ray is applied to it: it is obtained by 'bubbling, stretching, and flaking'. The resin: a resin can be used, and a conventionally known poly-smoke-based resin can be used, but it is preferably a heart 11 201037053 40% by mass or more. A polyolefin-based resin of a polyethylene-based resin obtained by using a quinone-based compound containing a tetravalent transition metal, and also by foaming the foam after the foam is foamed After being sliced in the direction of doubling, 'expanding and crusting with a hot roll, and manufacturing. In the foam base In the above, if necessary, any of the following additives may be added to the resin: a plasticizer, a softener, an antioxidant, a flame retardant, a fiber made of glass or plastic, a hollow ball (ball), a bead, a metal powder, etc. Fillers, colorants such as pigments and dyes, leveling agents, tackifiers, water repellents, defoamers, etc. In order to improve the adhesion to the adhesive layer or other layers, the foam substrate is used. It can also be subjected to surface treatment such as corona treatment, flame treatment, plasma treatment, hot air treatment, ozone/ultraviolet treatment, and application of an easy-adhesion treatment agent. In terms of surface treatment, by wetting agent-based wetting The index is 36 mN/m or more, preferably 4 〇mN//m or more, and more preferably 48 mN/m or more, and good adhesion to the adhesive can be obtained. [Adhesive layer] constituting the double-sided layer of the present invention Adhesive composition of an adhesive layer of an adhesive tape = characterized by 'cured by an acrylic adhesive composition containing an acrylic copolymer and a polymerized rosin-based adhesive-imparting resin' acrylic acid The copolymer contains a (meth)propionic acid 6 having a carbon number of 4 to 12 and a vinyl monomer having a repellent group as a monomer component. As a (meth)propyl group having a mosquito atom number of 4 to 12 Examples of the acid esters include: 'methyl (meth)acrylate, ethyl (meth)acrylate, n-butyl (meth)acrylate, isobutyl (meth)acrylate, t-butyl (meth)acrylate , (a) octyl acrylate, isooctyl (meth) acrylate, isophthalic acid (meth) acrylate 12 201037053 ester, cyclohexyl (meth) acrylate, 2-ethylhexyl (meth) acrylate One or two or more kinds of the monomers may be used. Among them, a (meth) acrylate having an alkyl group having 4 to 8 carbon atoms, particularly n-butyl acrylate, is easy to ensure adhesion to the adherend. It is preferable because it has excellent adhesion and cohesiveness and resistance to sebum. The content of the n-butyl acrylate is preferably 60% by mass or more, and more preferably 90% by mass or more, based on the total of (meth) acrylate having 4 to 12 carbon atoms. The content of the (meth) acrylate in the acrylic copolymer is preferably from 8 to 985 mass%, more preferably from 90 to 98. mass%, based on the monomer component of the acrylic copolymer. As the vinyl monomer having a carboxyl group, acrylic acid, methacrylic acid, itaconic acid, maleic acid, (meth)acrylic acid dimer, crotonic acid, ethylene oxide-modified succinic acid vinegar, and the like can be used. Among them, acrylic acid is preferably used as a copolymerization component. The content of the vinyl monomer having a carboxyl group in the acrylic copolymer is preferably from 5% to 1% by mass, more preferably from 1.5 to 5.0% by mass, based on 5% of the monomer component constituting the acrylic copolymer. Further, in the acrylic copolymer used in the adhesive composition constituting the adhesive layer of the double-sided adhesive tape of the present invention, a vinyl monomer having a tertiary amine skeleton in the molecule is preferably used as a monomer; The reason is that it is excellent in cohesive force and can suppress an excessive increase in adhesion. Therefore, polystyrene, (iv), acrylic, polycarbonate, polyacrylamide, polyacrylic acid, which are materials such as a casing and a member of an electronic device. Resin, such as resin, poly-resin, resin, and other metals such as residual steel, ingot, or zinc-plated steel, and glass, etc., can achieve good adhesion, reworkability, and re-peelability. 201037053 As a vinyl monomer having a tertiary amine skeleton in the molecule, N vinylpyrrolidone, N-vinyl caprolactam, acryloylmorpholine, n,n dimethyl decylamine, or the like can be used, among which It is preferred to use N-vinylpyrrolidone as a copolymerization component. The content of the vinyl monomer having a tertiary amine skeleton in the molecule in the acrylic copolymer is preferably from 5% to 5.0% by mass in the monomer component constituting the acrylic copolymer, more preferably from 15 to 3% by mass. Further, in the case where an isocyanate-based crosslinking agent is used as the crosslinking agent of the acrylic copolymer used in the present invention, as the vinyl monomer having a functional group reactive therewith, it is preferred to use a hydroxyl group-containing vinyl group. monomer. As the vinyl group-containing monomer having a mercapto group, for example, (mercapto)acrylic acid 24-based ethyl s, (meth)acrylic acid 2 _ propyl propyl vinegar, (meth) propylene sulphate L-butyl s-day (methyl) acrylic acid 6 • hexyl vinegar, etc., containing trans-based (meth) acrylate vinegar, especially preferably (meth) acrylate 2-meryl , (Meth)acrylic acid 4, butyl vinegar. The content of the radical-containing = dilute precursor which is reacted with the isocyanate-based crosslinking agent is preferably a monomer of the acid-based copolymer, particularly preferably 0.03 to 〇·3 mass%. . Examples of the vinyl monomer of 7 include: acetic acid B, 2, propylene, chiral amine, 2-mercaptopropanoic acid, etc., so-called t-yin's basal body; carbon number is 1~ 3 (meth) acrylate, the number of carbon atoms is based on (tetra) acid isobornyl, and stupid is two: (methyl (tetra) acid brewing, (a other of the other series of two:: vinyl single thought. i 5~2 0 in the monomer component is further composed of an acrylic acid copolymer, preferably 2 to 8 mass J, more preferably 1·5 to 1 "*%' adhesive The cohesive force ' Paula / can be easily adjusted, the force, and the adhesiveness are adjusted to a suitable range by being included in the range. 14 201037053 The acrylic copolymer can be known by a solution polymerization method such as a float polymerization method or an emulsion polymerization method. The polymerization method is used to: Γ 付 , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 黏 黏 黏 黏 , 黏 黏 , , , , , , , a thermal initiation method of a thermal polymerization initiator such as a peroxide-based nitrile such as a peroxide-based nitrile; (4) = _糸, benzoin, shouting, and poor technology #加Even acyl ketal, acyl phosphine oxide-based, benzoin

姻糸、—4甲_系的光聚合起始劑的紫外線照射引發方 法;電子射線照射方法。 就上述丙烯酸系共聚物的分子量而言,由凝膠渗透色 譜儀(G P C)測定之以料聚苯乙烯換算計的重量平均分子 量為40〜160萬’較佳為60〜120萬。 ,本發明使用的丙烯酸系黏著劑組合物中,為了兼顧與 被黏體的密合性和再加工適合性、再剝離性,因此較佳為 使用聚合松香酯系黏著賦予樹脂。聚合松香酯系黏著賦予 樹脂的軟化點為1〇〇〜18(rc,較佳為12〇它〜l6〇tt。 相對於丙烯酸系共聚物1 00質量份而言,聚合松香醋 系黏著賦予樹脂的配合量為1 〇〜40質量份、較佳為1 3〜3 〇 貞量份。此外’聚合松香酯系黏著賦予樹脂可使用1種或2 種以上。 另外’本發明使用的丙稀酸系黏著劑組合物中,出於 D周整與被黏體的密合性和再加工適合性、再剝離性的目 的’可使用聚合松香酯系黏著賦予樹脂以外的1種以上的 黏著賦予樹脂。作為其他的黏著賦予樹脂,呀例示:松香 系、聚合松香系、松香酚系、穩定化松香酯系、歧化松香 15 201037053 醋系、加氫松香醋系、箱稀系、祐烯㈣、石 基)丙稀酸醋系樹脂等 、…θ系、岬 況下,較^ 著麻合物的情 铨為使用乳液型的黏著賦予樹脂。 “其中’較佳為歧化松香酯系黏著賦予樹脂,松 黏:賦予樹脂,加氫松香醋系黏著賦 於 酯系樹脂,特佳為軟化點為60〜130t的歧化 賦予樹脂。 叹冗私杳s日糸黏者 使用其他的黏著賦予樹脂時的配合量,較佳為 丙烯酸系共聚物1〇〇質 5 的配合詈以下…松香酯系黏著賦予樹脂 , ,更佳為相對於丙烯酸系共聚% 100質量份 的黏著賦予樹脂的總量為10〜 銮盔访狄阁 1 错由使兩方的比 Μ祀圍,容易確保與被黏體的密合性。 丙烯酸系黏著劑組合物中,為 力,較佳為對黏著劑進行交聯。作劑層的凝聚 舉出:異氰酸…聯劑氧的,’可列 削衣軋系父聯劑,金屬螯合物系 交聯劑’氮丙咬系交聯劑等。其中’較佳為聚合沾束後添 加而進行交聯反應的類型的交聯劑;較佳為富有與(曱基、、 丙稀酸系共聚物的反應性的異氰酸I系交聯劑和環氧系交 聯劑;從提高與發泡體基材的密合性的方面考慮,更 異氰酸酯系交聯劑。 ‘ 料異氮酸醋系交聯劑’可列舉出:甲苯二異氛酸醋、 蔡獲-1,5 - 一異氰酸酉旨、六亞甲芙-υ备放& 八亞γ丞一異氰酸酯、二笨基甲烷 二異,酸醋、二甲苯二異氰酸醋、三羥甲基丙烷改性甲苯 二異氰酸醋等。特佳為3官能的聚異氰酸醋系化合物。作 為3 g能的異氰酸酯系化合物,可列舉出:甲笨二異氰酸 16 201037053 酉旨和它們的二經曱基丙炫·加成物、三笨基曱烧異氰酸g旨等。 作為交聯度的指標,使用了:對黏著劑層浸潰於甲苯 24小時後的不溶部分進行測定的凝膠分率的值。凝膠分率 較佳為25〜70質量%。更佳為30〜60質量%,最佳為33 〜55質量%,若位於該範圍時,凝集性和黏接性皆為良好。 此外’凝膠分率的測定基於下述。在剝離薄片上,使 乾燥後的厚度為65 # m地塗布黏著劑組合物,在1 〇(rc乾燥 ❹ 5分鐘、在40°C熟化2日,切成50mm見方,將其作為試樣。 接著,預先測定上述試樣的甲苯浸潰前的重量(G1),用3〇〇 目的金屬網,將在23。(:在甲苯溶液中浸潰24小時後的試樣 的甲苯不溶部分進行過濾,從而分離,測定在11〇它乾燥i 小時後的殘渣的重量(G2),按照下式來求出凝膠分率。 凝膠分率(質量%)=(G2/Gl)xl〇〇 作為添加劑,根據需要,可向黏著劑组合物中任意地 〇 添加·可塑劑,軟化劑,抗氧化齊!,玻璃、塑膠製纖維· 二“ Μ球珠•金屬粉末等填充劑,顏料•染料等著色劑, 調平劑’增黏劑’拒水劑’消泡劑等公知的添加劑。 “就本發明的雙面黏著帶所使用的黏著劑層巾言,在頻 率m:下顯不扣耗正切(u“)的極大值的溫度較佳為·3〇 c 1 〇 c。特別是想要提高低溫環境下的耐落下衝擊性之 時’更佳為-3(TC〜(TC,最佳為_25t〜_5t:。 另外,就本發明的雙面黏著帶而言,在頻率1HZ下顯 不損耗正切(ta…的極大值的溫度較佳為贼〜2(rc,更 17 201037053 佳為樹〜㈣,最佳為训〜rc。另夕卜,在頻率IHZ 時的損耗正切(tan<n的極大值為1〇以下,較佳為〇』以 下。籍由使黏著劑層的顯示損耗正切的極大值的溫度或雙 面黏著帶的損耗正切的極大值和顯示極大值的溫度為該範 圍便可谷易賦予本溫下的與被點體的良好的密合性與於〇 c以下的低溫環境下的耐落下衝擊性。 關於本發明的雙面黏著帶所使用的黏著劑層在 頻率1Η z時的儲存彈料描叙,广,、 仔弹性杈數(G ),只要滿足上述損耗正切 ㈣“)的範圍’就沒有特別規定,但是,當 性模數㈣為2.WPa以上’較佳為3加仏以上時, 可在如下情況下容易地賦予耐受性(氣密性)··氣密性高的電 子機器因機器溫度上升所伴隨的内壓的上升的情況;水深 lm的水壓((M 1MPa)以上的力從按壓剝離方向施加於由雙 面黏著帶固定的構件的情況。 —而样^ W (加5 ) ’從從基於溫度分散的動態黏彈性測 :獲传的儲存彈性模數(G,)、損耗彈性彈性模數(G,,),根 八,的式子求出。根據基於溫度分散的動態黏 弹丨生測…獲得某頻率下的損耗正切 顯示極大值的溫度。 斯大值和 稀酸系妓特^ ’可猎由適宜選擇出構成黏著劑的丙 燁-夂糸4物中所使用的單體的種類與 劑的種類與其使用量, :I起始 曰· i者賦予樹脂的種類與使用量’聚合方法等來調整。 據特定L就前述的黏著劑層的動態黏彈性特性而言,根 革、特疋溫度時的動態黏彈性頻譜的損耗正切、 18 201037053 或損耗正切和儲存彈性模數來規定,進—步,根據特定頻 率時之動態黏彈性頻譜的顯示損耗正切的極大值的溫戶, 或損耗正切的極大值來規定。在動態黏彈性的測定中Γ使 用黏彈性試驗機(Rheometric公司製,商品名.Infrared ray, a method of initiating ultraviolet irradiation of a photopolymerization initiator, and an electron beam irradiation method. With respect to the molecular weight of the above acrylic copolymer, the weight average molecular weight in terms of polystyrene measured by a gel permeation chromatograph (G P C) is from 40 to 1.6 million', preferably from 60 to 1.2 million. In the acrylic pressure-sensitive adhesive composition used in the present invention, in order to achieve compatibility with the adherend, reworkability, and removability, it is preferred to use a polymerized rosin ester-based adhesion-imparting resin. The polymerized rosin ester-based adhesion-imparting resin has a softening point of from 1 to 18 (rc, preferably 12 Å to 1600 tt.) Polymerized rosin-based vinegar-based adhesion-imparting resin with respect to 100 parts by mass of the acrylic copolymer The amount of the compound is from 1 to 40 parts by mass, preferably from 1 to 3 parts by weight. Further, one or two types of the polymerized rosin ester-based adhesion-imparting resin may be used. Further, the acrylic acid used in the present invention In the adhesive composition, one or more kinds of adhesion-imparting resins other than the polymerized rosin ester-based adhesion-providing resin can be used for the purpose of adhesion to the adherend and the reworkability and re-peelability of the D-week. As other adhesion-imparting resins, exemplified are: rosin, polymerized rosin, rosin phenol, stabilized rosin ester, disproportionated rosin 15 201037053 vinegar, hydrogenated rosin vinegar, box rare, ene (four), stone In the case of acetaminophen-based resin, etc., in the case of θ system or in the case of an alloy, an emulsion-type adhesion-imparting resin is used. "Where it is preferable to disproportionate rosin ester-based adhesion-imparting resin, loose-bonding: imparting a resin, hydrogenated rosin vinegar-based adhesive to an ester-based resin, particularly preferably a disproportionation-imparting resin having a softening point of 60 to 130 tons. In the case where the adhesive is used in the case of using another adhesive-imparting resin, it is preferably an acryl-based copolymer 1 〇〇 5 5 ... ... ... ... ... ... ... 酯 酯 酯 酯 酯 酯 酯 酯 酯 酯 酯 酯 酯 酯 酯 酯 酯 酯 酯 酯 酯 酯 酯 酯 酯 酯The total amount of the 100 parts by mass of the adhesion-imparting resin is 10 〜 銮 访 访 阁 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 For the force, it is preferred to crosslink the adhesive. The aggregation of the agent layer is as follows: isocyanic acid, oxygen, 'column coating, parent compounding agent, metal chelate crosslinking agent' nitrogen a C-crosslinking agent or the like. Among them, a crosslinking agent of a type which is preferably added after the polymerization is added to carry out a crosslinking reaction; preferably is rich in reactivity with a (meth) group or an acrylic copolymer. Isocyanate I crosslinking agent and epoxy crosslinking agent; from improvement and foaming In view of the adhesion of the substrate, a more isocyanate-based crosslinking agent is used. The term "isophthalic acid vinegar-based crosslinking agent" may be exemplified by toluene diisomeric acid vinegar and Cai get-1,5-isocyanuric acid.酉,六亚甲芙-υ备放amp & 八亚γ丞-isocyanate, di-peptidyl methane diiso, acid vinegar, xylene diisocyanate vinegar, trimethylolpropane modified toluene diisocyanate A vinegar or the like is particularly preferably a trifunctional polyisocyanate-based compound. Examples of the 3 g-enable isocyanate-based compound include methyl acetoise diisocyanate 16 201037053 and their diterpene-based fluorene. The addition product, the tribasic sulfonium isocyanate g, etc. As an index of the degree of crosslinking, the value of the gel fraction of the insoluble portion after the adhesive layer was immersed in toluene for 24 hours was used. The gel fraction is preferably from 25 to 70% by mass, more preferably from 30 to 60% by mass, most preferably from 33 to 55% by mass, and if it is in this range, both cohesiveness and adhesion are good. The gel fraction was measured based on the following. On the release sheet, the adhesive composition was applied to a thickness of 65 # m after drying, at 1 〇 (r c Drying ❹ 5 minutes, aging at 40 ° C for 2 days, cutting into 50 mm square, and using this as a sample. Next, the weight (G1) before toluene impregnation of the above sample was measured in advance, and a metal mesh of 3 mesh was used. (2: The toluene-insoluble portion of the sample after being immersed in the toluene solution for 24 hours was filtered, and separated, and the weight (G2) of the residue after drying for 1 hour at 11 Torr was measured, and the following formula was used. The gel fraction is determined. Gel fraction (% by mass) = (G2/Gl) xl 〇〇 As an additive, if necessary, it can be arbitrarily added to the adhesive composition, a plasticizer, a softener, and an antioxidant. Qi!, glass, plastic fiber, two "Μ ball beads, metal powder and other fillers, colorants such as pigments and dyes, leveling agents, 'tackifiers', water repellents, defoamers, and other known additives. "As for the adhesive layer of the double-sided adhesive tape of the present invention, the temperature at which the maximum value of the tangent (u" is not deduced at the frequency m: is preferably 3 〇 c 1 〇 c. In particular, when it is desired to improve the drop impact resistance in a low-temperature environment, it is more preferably -3 (TC~(TC, preferably _25t~_5t:. Further, in the double-sided adhesive tape of the present invention, The frequency of 1HZ is not lossy tangent (the temperature of the maximum value of ta... is preferably thief ~ 2 (rc, more 17 201037053 good for tree ~ (four), best for training ~ rc. In addition, loss at frequency IHZ Tangent (tan<n has a maximum value of 1 〇 or less, preferably 〇 以下 or less.) The maximum value of the loss tangent of the double-sided adhesive tape and the maximum value of the tangent by the temperature at which the display loss of the adhesive layer is tangent. When the temperature is within this range, it is easy to impart good adhesion to the object at the present temperature and fall impact resistance in a low-temperature environment of 〇c or less. The double-sided adhesive tape used in the present invention is used. The storage trajectory of the adhesive layer at a frequency of 1 Η z, the wide, and the elastic number (G), as long as the above-mentioned loss tangent (four) ") range is not specified, but when the modulus (four) is 2. When WPa or more is preferably 3 or more, it is easy to impart resistance in the following cases. The electronic device with high visibility (airtightness) and airtightness increases the internal pressure due to the increase in the temperature of the machine. The water pressure of the water depth lm (the force of (M 1 MPa) or more is applied from the press-peeling direction to The case where the double-sided adhesive tape is fixed. -When the sample is W (plus 5) 'From the dynamic dispersion measurement based on temperature dispersion: the stored elastic modulus (G,), loss elastic modulus (G) ,,), the root eight, the formula is obtained. According to the temperature-dispersion dynamic viscoelastic test... obtain the loss tangent at a certain frequency to show the maximum temperature. The large value and the dilute acid system ^ ' can The types and the types of the monomers used in the preparation of the binders and the materials used in the preparation of the adhesives are selected, and the type and amount of the monomers to be used are: According to the specific L, the dynamic viscoelastic properties of the above-mentioned adhesive layer are defined by the loss tangent of the dynamic viscoelastic spectrum at the root temperature, the characteristic temperature, 18 201037053 or the loss tangent and the storage elastic modulus. Step-by-step, dynamic viscoelasticity at a specific frequency The characteristic spectrum of the loss spectrum is the maximum value of the tangential value of the temperature, or the maximum value of the loss tangent. In the measurement of dynamic viscoelasticity, the viscoelasticity tester (trade name, manufactured by Rheometric Co., Ltd.) is used.

AreUKSTD),在該試驗機的作為測定部的平行圓^之間夹 入試驗片,以頻率1Hz敎從_贼至丨㈣㈣存彈_ 數(G’)和損耗彈性彈性模數(〇就試驗片而言,將黏著劑 層或雙面黏著帶形成為厚度約2mm,夾於平行圓盤之間, 進行測定。 ^就本發明使用的黏著劑層的厚度而言,從即使在製 薄型的膠帶的情況下也容易確保與被黏體的密合性以及再 加工適合性、再剝離性的方面考慮,單面的厚度較佳為Μ 〜100/zm,更佳為30〜80 "m。AreUKSTD), the test piece was sandwiched between the parallel circles of the measuring machine as the measuring unit, and the frequency was measured at a frequency of 1 Hz from the _ thief to the 丨 (four) (four) 弹 _ number (G') and the loss elastic modulus (〇 test In the case of the sheet, the adhesive layer or the double-sided adhesive tape is formed to have a thickness of about 2 mm and sandwiched between the parallel discs for measurement. ^ As far as the thickness of the adhesive layer used in the present invention is concerned, from the thinner In the case of the tape, it is also easy to ensure adhesion to the adherend, reworkability, and re-peelability, and the thickness of one side is preferably Μ100/zm, more preferably 30 to 80 "m .

作為本發明使用的剝離薄片,雖然沒有特別限定,但 可例示:在聚乙烯、聚丙烯、聚酯膜等的合成樹脂膜,紙, 不織布十發泡薄片或金屬箱,以及它們的積層體等的 基材的至少單面上’實施了用於提高從黏著劑剝離的剥離 性的有機石夕系處理、長鏈烧基系處理,處理等 理的剝離薄片。 和聚酯膜的單 其中’較佳為:在積層了聚乙烯的紙、 面’實施了有機石夕系剝離處理的剝離薄片。 〔雙面黏著帶〕 就本發明的雙面黏著帶而 材和黏著劑層,顯示出與被黏 生發泡體基材的層間損壞,另 言,通過使用上述發泡體基 體的適宜的密合性,不易發 外由於即使在產生了層間裂 19 201037053 痕的情况 …,μ仏个霄殘留於構件表面從而容易剝離, 因此,在可攜式電子機器等的製造時,將未成功地接合於 未70成的雙面黏著帶、構件等進行剝離(再加工)的情况下, 以及在| 了對可攜式電子機器等完成口。口進行修理或再生、 再矛!用而將殼體、構件進行分離•分解•解體的情况下, 可改善從忒體、構件去除雙面黏著帶之後重新貼合新的雙 面黏著帶的作業的效率,構件等的良率以及回收率。進-步’在具有防水功能的電子機器的構件的固定方面,可有 效地防止水從密合間隙的浸人,具有優異的防水功能。 、作為本發明的雙面黏著帶的實施方心基本結構為: 、發/包體基材為中芯’在該基材的兩面設置有黏著劑層的 結構。基材與黏著劑層之間可直接地層疊,也可具有其他 的層。这些形態只要根據使用用途來適宜選擇即可,進一 步賦予膠帶以尺寸穩定性、拉伸強度的情況下,可設置聚 醋膜等的層㈣;賦予朦帶以遮光性的情況下,可設置遮 光層;確保光反射性時,可設置光反射層。在設置有這些 其他的層的情況下,使用防水性的層作為該其他的層。 膜。α ^、、曰麼層彳使用以聚醋膜為代表的各種樹脂製 、從毛泡體基材的跟隨性的方面老唐 π万面考慮’该等之厚度較佳 马I〜更佳為3〜12#m。 作為遮光層,可簡便地使用由 Μ ,, ^ ώ 另顏科等者色劑的油 故::的遮光層,由黑油墨形成的層,由於遮光性優里, 文可較佳使用。作為反射層’可簡便地使用由白色油^ 成的層。作為這些層的厚度,較佳 … 平乂住馬2〜2〇以m,其中 6心。藉由使厚度位於該範圍,不易產生由油墨的固 20 201037053 化收縮導致的基材的捲曲’膠帶的加工性良好。 本發明的雙面黏著帶可根據公知慣用的方法來製造。 :列舉出:例如’直接地在發泡體基材上,或者在層疊於 :泡體基材上的其他的層的表面上,冑丙烯酸系黏著劑組 :物進仃塗布、乾燥的直接印法;或在剝離薄片上將丙烯 ,糸黏著劑組合物塗布、乾燥之後,貼合於發泡體基材、 -他的層的表面的轉印法。較佳》’在剝離薄片上將丙烯 θThe release sheet used in the present invention is not particularly limited, and examples thereof include a synthetic resin film such as polyethylene, polypropylene, or a polyester film, paper, a non-woven ten-foamed sheet or a metal case, and a laminate thereof. On at least one side of the base material, a release sheet having an organic stone treatment, a long-chain base treatment, a treatment, and the like for improving the peeling property from the adhesive is performed. And a single sheet of the polyester film, which is preferably a release sheet which has been subjected to an organic stone peeling treatment on a paper or a sheet in which polyethylene is laminated. [Double-sided adhesive tape] The double-sided adhesive tape of the present invention and the adhesive layer exhibit interlayer damage to the adhered foam substrate, in other words, by using the above-mentioned foam base for proper adhesion Sexuality, it is not easy to send out. Even in the case where the interlayer crack 19 201037053 is produced, μ仏 is left on the surface of the member to be easily peeled off, so that it is unsuccessfully bonded to the manufacture of a portable electronic device or the like. When 70% of the double-sided adhesive tape, members, and the like are peeled off (reworked), and the portable electronic device or the like is completed. The port is repaired or regenerated, and the spears are used. When the casing and the member are separated, and the disassembled and disassembled, the double-sided adhesive tape is removed from the carcass and the member, and the new double-sided adhesive tape is reattached. Efficiency, yield of components, etc. and recovery. In the step of fixing the member of the electronic device having the waterproof function, it is possible to effectively prevent the water from being immersed from the close gap and has an excellent waterproof function. The basic structure of the embodiment of the double-sided adhesive tape of the present invention is as follows: The hair/package substrate is a core core. A structure in which an adhesive layer is provided on both surfaces of the substrate. The substrate and the adhesive layer may be directly laminated or may have other layers. These forms may be appropriately selected depending on the intended use, and when the tape is further provided with dimensional stability and tensile strength, a layer (four) such as a polyester film may be provided; and when the tape is provided with light blocking properties, light shielding may be provided. Layer; when ensuring light reflectivity, a light reflecting layer may be provided. In the case where these other layers are provided, a water-repellent layer is used as the other layer. membrane. α^, 曰 曰 layer 彳 各种 各种 彳 彳 彳 彳 彳 各种 各种 各种 各种 各种 各种 各种 α α α α α α α α α α α α α α α α α α α α α α α α α α α α 3~12#m. As the light-shielding layer, it is possible to easily use a light-receiving layer of a coloring agent such as yttrium, yttrium, or the like, and a layer formed of a black ink, which is preferably used as a light-shielding property. As the reflective layer ', a layer made of white oil can be used simply. As the thickness of these layers, it is preferable to hold the horse 2 to 2 inches in m, of which 6 hearts. When the thickness is within this range, the curl of the substrate caused by the shrinkage of the ink is not easily generated. The workability of the tape is good. The double-sided adhesive tape of the present invention can be produced according to a conventionally known method. : exemplified by, for example, 'directly on the foam substrate, or on the surface of other layers laminated on the foam substrate, the enamel acrylic adhesive group: direct printing of the coating and drying Or a transfer method in which a propylene and ruthenium adhesive composition is applied and dried on a release sheet, and then bonded to a surface of a foam substrate and a layer thereof. Preferred"' propylene θ on the release sheet

G 酸系黏著劑組合物塗布、乾燥後,貼合於發泡體基材、其 他的層的表面的轉印法。 本發明的雙面黏I帶的厚度根據使用㈣來適宜調整 P可為70〜14〇〇 " m。在電子機器的構件的固定用的情況 下,特別是小型、薄型的可攜式電子機器的情況下,由於 要求薄的膠帶厚度’故較佳為1〇〇〜6〇〇”,特佳為12〇" m〜500 "m。通過使膠帶厚度為該厚度,還可適宜地適用於 薄型·小型的可攜式電子機H,另外可實現良好的防水功 就本發明的雙面黏著帶而言,藉由下述測定條件測定 的面黏接強度卜較佳為⑽N/W以上,更佳為ΐ3〇Ν/ 4cm2以上。 上述面黏接強度1的測定條件如下。 ^ υ在23°C,在厚度2mm的5cm見方的丙烯酸板上,平 行地貼附2張的寬度5mm長度4cm的雙面黏著帶。 )接著將由1)製成的附有雙面黏著帶的丙稀酸板, 以丙烯酸板的中心肖ABS板的中心—致的方式,貼附於: 在中心部設置有直徑lem的孔的厚度2mm、10xl5em的長 21 201037053 /的平π的ABS板上,以2kg的輥進行i個來回的加壓 之後’在23 °C放置1小時,作為試驗片。 3)從試驗片的ABS侧藉由abs板的孔,用安裝有直徑 8醜的不銹鋼製探針的拉伸試驗機,以l〇_/min將丙烯 酸板進行按壓,測定出剝離丙烯酸板的強度。After the G-acid adhesive composition is applied and dried, the transfer method is applied to the surface of the foam substrate and other layers. The thickness of the double-sided adhesive tape of the present invention can be suitably adjusted according to the use of (4) P can be 70 to 14 〇〇 " m. In the case of fixing the components of the electronic device, particularly in the case of a small and thin portable electronic device, since a thin tape thickness is required, it is preferably 1 〇〇 to 6 〇〇, which is particularly preferable. 12〇" m~500 "m. By making the thickness of the tape to this thickness, it is also suitable for a thin and small portable electronic machine H, and in addition, good waterproof work can be achieved on the double-sided adhesive of the present invention. The surface bonding strength measured by the following measurement conditions is preferably (10) N/W or more, more preferably ΐ3 〇Ν / 4 cm 2 or more. The measurement conditions of the surface bonding strength 1 are as follows. °C, two double-sided adhesive tapes of 5 mm in length and 4 cm in length were attached in parallel on a 5 cm square acrylic plate having a thickness of 2 mm.) Then, an acrylic plate with a double-sided adhesive tape made of 1) was attached. In the center of the center of the acrylic plate, the center of the ABS plate is attached to: the thickness of the hole with the diameter lem at the center is 2mm, the length of 10xl5em is 21 201037053 / the flat π ABS plate, with 2kg After the roller was subjected to i pressurization, it was placed at 23 ° C for 1 hour as a test. 3) From the ABS side of the test piece, the acrylic plate was pressed at 10 〇/min by a tensile tester equipped with a stainless steel probe having a diameter of 8 mm by the hole of the abs plate, and the peeled acrylic plate was measured. Strength of.

另外,就本發明的雙面黏著帶而言,根據下述測定條 件測疋的面黏接強度2較佳為250mJ以上,更佳為350mJ 以上。 上述面黏接強度2的測定條件如下。 1)將雙面黏著帶切斷成2cm見方之後,貼附於厚度 2mm、2cm見方的丙烯酸板。 2) 將附有雙面黏著帶的丙烯酸板,以丙烯酸板的中心部 與聚醯胺板的中心部一致的方式,貼附於:在中心部具有 直铨lcm的孔之厚度2mm的4cm見方的聚醢胺板(添加有 〇負里/6玻璃纖維)上,以2kg的輥進行i個來回的加壓之 後,在23t放置24小時,作為試驗片。 3) 將試驗片設置於外形4cm見方的高度3cm、厚度 的不銹鋼製的台座,並使聚醯胺側朝上。 4) 藉由聚醯胺侧的孔,朝向丙烯酸板,使前端具有直徑 5mm、長度lcm的突起的重量1〇〇g的黃銅製圓錐從高度 l〇cm起,以10cm間隔來連續落下(每i階段3次),測定: 在試驗片確認出膠帶的剝離、損壞時的高度。 5) 根據測定結果來算出:落下能量mJ(=98x高度⑽)x 100g) 〇 就本發明的雙面黏著帶而言,即使為薄的膠帶厚度也 22 201037053 顯不出與被黏體的良好的黏接 性和再剝離性。因此,在為了提性以及再加工適合 良率而將去+ 為了如南電子機器等的製造時的 良羊而將未成功地接合於未 進行剝離⑴、 的雙面黏著帶、構件等 再生J )的情况下,或在為了將完成品進行修理或 况下等Γ用而,殼體、構件進行分離•分解•解體的情 貼合作業效率,禮杜制σ & 乂回了·重新 使用形良率和回收率。作為具體的 Ο Π 用於:在電子筆記本、手機、PHS、照 目機、音樂播放器、電視等電子機 一 _ 的保護面板與殼體的貼合,殼此二貧訊顯示部 數位鍵、觸摸板等輸人裝置:::此片狀 107貼口,忒體和裝飾用薄片的 σ,/、他各種構件、模組的固定等。 另外,就本發明的雙面黏著帶而言,即使為薄的膠帶 厚度也顯示出與被黏體的適宜的密合性,可有效地防止水 從d間隙的浸入,具有優異的防水功能。因此,對於薄 ❹型化提高、殼體内的容積限制嚴格、難以另行設置水密封 :段的可攜式電子機ϋ等而言,也可有效地賦予防水功 能。作為具體的使用形態,可適宜地用於:在電子筆記本、 手機PHS、照相機、音樂播放器、電視等可攜式電子機器 方面的,資訊顯示部的保護面板與殼體的貼合,殼體彼二 的貼合’殼體和片狀數位鍵、觸摸板等輸入裝置的貼合, 喊體和裝飾用薄片的貼合,其他各種構件、模組的固定等。 另外,對於使用了橡谬製密封圈(packing)、塾圈、封閉劑等 以往的水密封手段的部分’也可在有效地賦予防水功能的 同時’容易將殼體、構件進行分離•分解•解體,以將完 23 201037053 成品進行修理或再生、再利用。 實施例 (黏著劑溶液A的調製) 在具備攪拌機、回流冷凝器、溫度計、滴液漏斗以及 氮氣導入〇的反應容器中,將丙烯酸丁酯93.54質量份、乙 酸乙烯酯3質量份、丙烯酸2.2質量份、N-乙烯基_2_D比洛 烷酮1_2質量份、丙烯酸4-羥基丁酯0.06質量份、作為聚 合起始劑的2,2’-偶氮二異丁腈〇_1質量份,溶解於由1〇〇 質量份乙酸乙酯構成的溶劑中,在601聚合12小時,從而 獲得重量平均分子量為70萬(以聚笨乙烯換算)的丙烯酸系 共聚物。接著,相對於丙烯酸系共聚物1 〇〇質量份,添加 荒川化學公司製PENSELD135(聚合松香的季戊四醇酷,軟 化點135°C )15質量份、荒川化學公司製SUPEr ESTERAl〇() (歧化松香的甘油酯,軟化點100°c ) 12質量份,加入乙酸乙 酯’均勻地混合’從而獲得不揮發成分為40%的黏著劑溶 液A。 (黏著劑溶液B的調製) 在具備擾拌機、回流冷凝器、溫度計、滴液漏斗以及 氮氣導入口的反應容器中,將丙稀酸丁酯74.9質量份、丙 烯酸2-乙基己酯20質量份、丙烯酸2質量份、乙酸乙稀酿 3質量份、丙烯酸4-羥基丁酯0· 1質量份 '作為聚合起始劑 的2,2’-偶氮二異丁腈〇· 1質量份,溶解於由1〇〇質量份乙 酸乙酯構成的溶劑中’在70 C聚合12小時,從而獲得重量 平均分子量為50萬(以聚苯乙烯換算)的丙烯酸系共聚物。 接著’相對於丙烯酸系共聚物100質量份,添加25質量份 24 201037053 的荒川化學公司製PENSEL D135,加入乙酸乙酯,均勻地 混合’從而獲得不揮發成分為5〇%的黏著劑溶液B。 〔實施例1〕 (雙面黏著帶的調製)Further, in the double-sided adhesive tape of the present invention, the surface adhesive strength 2 measured according to the measurement conditions described below is preferably 250 mJ or more, more preferably 350 mJ or more. The measurement conditions of the above-mentioned surface bonding strength 2 are as follows. 1) After cutting the double-sided adhesive tape into 2 cm square, it was attached to an acrylic plate having a thickness of 2 mm and 2 cm square. 2) The acrylic plate with the double-sided adhesive tape is attached to the center of the acrylic plate in the same manner as the center of the polyimide plate, and is attached to a 4 cm square having a thickness of 2 mm in a hole having a diameter of 1 cm at the center. The polyimide plate (with the addition of the vinegar/6 glass fiber) was subjected to i-back pressure with a 2 kg roller, and then placed at 23 t for 24 hours to serve as a test piece. 3) The test piece was placed on a stainless steel pedestal having a height of 3 cm and a thickness of 4 cm square, and the polyamine side was turned upward. 4) With the polyacetamide side hole facing the acrylic plate, the brass cone having a diameter of 5 mm and a length of 1 cm and having a length of 1 cm from the height l〇cm is continuously dropped at intervals of 10 cm (each I stage 3 times), measurement: The height at which the tape was peeled off or damaged was confirmed in the test piece. 5) Calculated based on the measurement results: drop energy mJ (=98x height (10)) x 100g) 〇 For the double-sided adhesive tape of the present invention, even if the thickness of the tape is thin, 22 201037053 does not show good adhesion to the adherend. Adhesiveness and re-peelability. Therefore, it is unsuccessfully joined to the double-sided adhesive tape, member, etc. which is not peeled off (1) for the good sheep at the time of manufacture, such as a South electronic machine, for the sake of improvement and rework. In the case of the case, in order to repair or use the finished product, the housing and the components are separated, decomposed, and disassembled, and the efficiency of the cooperation is ritual, and the ritual σ & Shape yield and recovery. As a specific Ο Π used for: in the electronic notebook, mobile phone, PHS, eye-catching machine, music player, TV and other electronic devices, the protective panel and the housing, the shell of the two poor display display digital keys, Touch panel and other input devices::: This sheet of 107 sticks, σ of the body and decorative sheets, /, his various components, the fixing of the module, and so on. Further, in the double-sided adhesive tape of the present invention, even a thin tape thickness exhibits an appropriate adhesion to the adherend, and it is possible to effectively prevent water from entering from the d gap and have an excellent waterproof function. Therefore, the waterproof function can be effectively imparted for the improvement of the thinning type, the strict volume limitation in the casing, and the difficulty in providing a separate water seal: the portable electronic case of the segment. As a specific use form, it can be suitably used in the case of a portable electronic device such as an electronic notebook, a mobile phone PHS, a camera, a music player, a television, etc., the protective panel of the information display part is attached to the casing, and the casing The second one is a combination of a housing, a sheet-like numeric key, a touch panel and the like, an attachment of a shouting body and a decorative sheet, and fixing of various other members and modules. In addition, the part 'which is a conventional water-sealing means such as a rubber seal, a ring, or a sealant can effectively separate the casing and the member while dissolving the waterproof function. Disintegration to repair, regenerate and reuse the finished product of 2010 201037053. EXAMPLES (Preparation of Adhesive Solution A) 93.54 parts by mass of butyl acrylate, 3 parts by mass of vinyl acetate, and 2.2 mass of acrylic acid in a reaction vessel equipped with a stirrer, a reflux condenser, a thermometer, a dropping funnel, and a nitrogen introduction crucible Parts, N-vinyl 2_D 1 2 parts by mass of cropirone, 0.06 parts by mass of 4-hydroxybutyl acrylate, 2,2'-azobisisobutyronitrile 〇_1 parts by mass as a polymerization initiator, dissolved In a solvent composed of 1 part by mass of ethyl acetate, it was polymerized at 601 for 12 hours to obtain an acrylic copolymer having a weight average molecular weight of 700,000 (in terms of polystyrene). Then, 15 parts by mass of PENSELD 135 (fine pentaerythritol of polymerized rosin, softening point 135 ° C) manufactured by Arakawa Chemical Co., Ltd., and SUPEr ESTER Al(R) manufactured by Arakawa Chemical Co., Ltd. (disproportionated rosin) were added to 1 part by mass of the acrylic copolymer. Glyceryl ester, softening point 100 ° c) 12 parts by mass, added with ethyl acetate 'evenly mixed' to obtain an adhesive solution A having a nonvolatile content of 40%. (Preparation of Adhesive Solution B) In a reaction vessel equipped with a scrambler, a reflux condenser, a thermometer, a dropping funnel, and a nitrogen introduction port, 74.9 parts by mass of butyl acrylate and 2-ethylhexyl acrylate 20 were used. Parts by mass, 2 parts by mass of acrylic acid, 3 parts by mass of ethyl acetate, 0. 1 part by mass of 4-hydroxybutyl acrylate, 2,2'-azobisisobutyronitrile, 1 part by mass as a polymerization initiator It was dissolved in a solvent composed of 1 part by mass of ethyl acetate to be polymerized at 70 C for 12 hours to obtain an acrylic copolymer having a weight average molecular weight of 500,000 (in terms of polystyrene). Then, 25 parts by mass of PENSEL D135 manufactured by Arakawa Chemical Co., Ltd., 24, 2010, 530, and the like, and ethyl acetate was added thereto and uniformly mixed to obtain an adhesive solution B having a nonvolatile content of 5% by weight. [Example 1] (Modulation of double-sided adhesive tape)

相對於上述黏著劑溶液A 100質量份,添加1.24質量 伤的曰本聚胺酯公司製“ C〇ronate L-45”(異氰酸g旨系交聯 劑,固體成分45% ),攪拌15分鐘後,在進行過剝離處理 的厚度75# m的pet膜上塗布,使乾燥後的厚度為35#m, 在8 0 C乾燥3分鐘,形成黏著劑層。 接著,在白色聚烯烴系發泡體(厚度:13〇 # m,發泡倍 率2.5倍25%壓縮強度.130kPa,拉伸彈性模數:丨14〇n /cm2’拉伸強度14.8N/cm,表面經電暈處理的潤濕指數 為52mN/m)的兩面上,貼合各i張前述黏著薄片之後,採 用線壓5kg/cm的輥進行層壓。其後,在4〇。〇孰化48 從而獲得厚度200#m的雙面黏接薄片。 ’ 〔實施例2〜5〕 除了使用表 . “ 戰料泡體基材來替代白色聚稀煙系 發泡體,將黏著劑的乾燥後的厚度變 ’、 文文為表1所示的厚 以外,藉由與實施例1相同的方法來 又 ,^ 木獲侍雙面黏著帶。 〔實施例6〕 ,而添加0.8質量 (異氰酸醋系交聯 相同的方法來獲 除了相對於黏著劑溶液A 1 〇〇質量份 份的日本聚胺酯公司製‘‘coronate l_45,, 劑,固體成分45%)以外,藉由與實施例工 得雙面黏著帶。 〔實施例7、8〕 25 201037053 相對於上述黏著劑溶液㈣。質量份,添加2 ()f量份 :曰本聚胺醋公司t “C〇r〇nate “5”(異氰酸醋系交聯 Μ ’固體成分45%),授拌15分鐘後,在進行過剝離處理 的厚度75^的PET膜上塗布,使乾燥後的厚度為表"斤 示的厚度,在80T:乾燥3分鐘,從而形成黏著劑層。除了 使用該黏著劑層以外,藉由與實施例丨相同的方法來浐广 雙面黏著帶。 又Τ 〔實施例9〕 替代白色聚烯烴系發泡體,在黑色乙烯_乙酸乙烯醋系 發泡體(厚度:800 # m,發泡倍率8倍,25%壓縮強度: 34kPa ’拉伸強度:24 8N/ cm,表面經電暈處理的潤濕指 數為52mN/m)的兩面上,相對於黏著劑溶液B 1〇〇質量份 添加2.0質量份的日本聚胺酯公司製“c〇r〇nate L_45,,(異 氰酸酯系交聯劑,固體成分45%),攪拌15分鐘後,在進 行過剝離處理的厚度75#m的pet膜上塗布,使乾燥後的 厚度為50#m,在8(rc乾燥3分鐘,從而形成黏著劑層。 除了使用該黏著劑層以外,藉由與實施例8相同的方法來 獲得雙面黏著帶。 〔實施例10〕 (黏著劑溶液F的調製) 在具備攪拌機、回流冷凝器、溫度計、滴液漏斗以及 氣氣導入口的反應容器中,將丙烯酸丁酯85.9質量份、丙 烯酸4質量份、曱基丙烯酸甲基10質量份、丙烯酸4-羥基 丁 S旨0.1質量份、作為聚合起始劑的2,2,_偶氮二異丁腈 質量伤谷解於由1 〇〇質量份乙酸乙酯構成的溶劑中,在 26 201037053 6(TC聚合12小時,從而獲得重量平均分子量為7q萬(以聚 苯乙婦換算)的丙烯酸系共聚物。接著,相對於丙稀酸系共 聚物100質量份,添加荒川化學公司製penseldi6〇(聚合 松香的季戊四醇醋)10質量份、由甲基丙烯酸環己醋97質 量份、丙烯酸3質量份構成的丙烯酸類樹脂(重量平均分子 量:6000,玻璃化溫度:66。〇1〇質量份,加入乙酸乙醋, 均勻地混合,從而獲得不揮發成分30%的黏著劑溶液F。 (雙面黏著帶的調製) 相對於上述黏著劑溶液F 100質量份,添加〇·9質量份 的日本聚胺酯公司t “ C〇ronate L_45”(異氰酸酯系交聯 劑,固體成分45%),搜拌15分鐘後,在進行過剝離處理 的厚度75^m的PET膜上塗布,使乾燥後的厚度為 在80°C乾燥3分鐘,從而形成黏著劑層。除了使用該黏著 劑層以外,藉由與實施例1相同的方法來獲得雙面黏著帶。 〔實施例11〕 (黏著劑溶液G的調製) t在具備授拌機、回流冷凝器、溫度計、滴液漏斗以及 氮氣導入口的反應容器中,將丙烯酸丁酯71.9質量份、丙 烯酸2-乙基己酯2〇質量份、丙烯酸5質量份、丙烯酸甲酯 3質量份、丙烯酸2-羥基乙酯〇.!質量份、作為聚合起始劑 的2,2’-偶氮二異丁腈(M f量份,溶解於由乙酸乙酯⑽ 質量份構成的溶劑中…(TC聚合12小時,從而獲得重量 平均分子量為60萬(以聚苯乙烯換算)的丙烯酸系共聚物。 接著’相對於丙烯酸系共料勿1〇〇質,量份,添加荒川化學 公司製PENSEL D135(聚合松香的季戊四醇醋)別質量份、 27 201037053 yasUHARA CHEMICAL公司製τΐ6〇紛⑽質量份, 加入乙酸乙酿,均勻地尾人 ,從而獲侍不揮發成分4S%的 黏著劑溶液G。 (雙面黏著帶的調製) 相對於上述黏著劑溶液Gl〇〇質量份,添加"質奸 的曰本聚胺醋公司t “CoronateL_45”(異氮酸醋系交聯 劑’固體成分45%)’授拌15分鐘後’在進行過剝離處理 的厚度〜m的而膜上塗布,使乾燥後的厚度為Μ心, 在80C乾燥3分鐘,從而形成黏著劑層。除此以外,藉由 與實施例1相同的方法來獲得雙面黏著帶。 〔比較例1、2〕 除了使用表2記載的發泡體基材來替代白色聚婦煙系 發泡體以外’藉由與實施例丨相同的方法來獲得雙面黏著 帶。 〔比較例3〕 除了使用不織布(單位面積重量:17g/m2,拉伸強产· IWNAm)來替A白色聚稀㈣發泡冑’使用乾燥後的又厚 度為70/zm的黏著劑以外,藉由與實施例i相同的方法來 獲得雙面黏著薄片。 〔比較例4〕 除了使用聚對苯二曱酸乙二醇醋(PET)製膜(厚度:⑽ 一拉伸強度:210N/cm,表面經電暈處理的潤濕指數 為52mN/m)來替代白色聚稀煙系發泡體,並且& 燥後的厚度為表中記載的以外,藉由與實施例"目同二: 法來獲得雙面黏著薄片。 28 201037053 [比較例5] (黏著劑溶液C的調製) • 在具備攪拌機、回流冷凝器、溫度計、滴液漏斗以及 氮氣導入口的反應容器中,將丙烯酸丁酯93.;54質量份、乙 酸乙烯酯3質量份、丙烯酸2.2質量份、N-乙烯基比洛 烷酮1.2質量份、丙烯酸4-羥基丁酯〇.〇6質量份、作為聚 合起始劑的2,2’ -偶氮二異丁腈0.1質量份,溶解於由乙酸 乙酯100質量份構成的溶劑中,在60°C聚合12小時,從而 C| 獲得重量平均分子量為70萬(以聚苯乙烯換算)的丙稀酸系 共聚物。接著,相對於丙烯酸系共聚物100質量份,添加 25質量份的荒川化學製SUPER ESTER A 100作為黏著賦予 樹脂,加入乙酸乙酯,均勻地混合,從而獲得不揮發成分 40%的黏著劑溶液C。 (雙面黏著帶的調製) 相對於上述黏著劑溶液C 1〇〇質量份,添加1 ·〇質量份 ❹的日本聚胺酯公司製“ Coronate L -45”(異氰酸酯系交聯 劑,固體成分45%),攪拌15分鐘後,在進行過剝離處理 的厚度75# m的PET膜上塗布,使乾燥後的厚度為乃以瓜, 在80°C乾燥3分鐘,從而形成黏著劑層。除此之外,藉由 與實施例1相同的方法來獲得雙面黏著帶。 " 〔比較例6〕 (黏著劑溶液D的調製) 在具備授摔機、回流冷凝哭、、、w译斗 |(·今凝益、溫度计、滴液漏斗以及 氮氣導入口的反應容器中,將丙烯酸丁酯97 9質量份、丙 稀酸2_G質量份、丙稀酸4,基丁 0旨Q1 f量份、作為聚合 29 201037053 起始劑的2,2,-偶氮二異丁腈〇」質量份,溶解於由1〇〇質 $份乙酸乙酯構成的溶劑中,在701聚合12小時,從而獲 得重量平均分子量為8〇萬(以聚苯乙烯換算)的丙烯酸系共 聚物。接著,加入乙酸乙酯,均勻地混合,從而獲得不揮 發成分3 0 %的黏著劑溶液d。 (雙面黏著帶的調製) 相對於黏著劑溶液D 1〇〇質量份,添加2.5質量份的曰 本聚胺酯公司製“Cor〇nate L_45”(異氰酸酯系交聯劑,固 體成刀45/6),攪拌15分鐘後,在進行過剝離處理的厚度 75/zm的PET膜上塗布,使乾燥後的厚度為5〇#m,在8〇 C乾燥3分鐘而形成黏著劑層。除此之外,藉由與實施例i 相同的方法來獲得雙面黏著帶。 〔比較例7〕 (黏著劑溶液E的調製) 在具備攪拌機、回流冷凝器、溫度計、滴液漏斗以及 氮氣導入口的反應容器中,將丙烯酸2-乙基己酯98質量 份、丙烯酸1質量份、丙烯酸4-羥基丁酯1質量份、作為 聚合起始劑的2,2,·偶氮二異丁腈0.1質量份,溶解於由100 質董份乙酸乙醋構成的溶劑中,在701聚合1 2小時,從而 獲付重置平均分子量為80萬(以聚苯乙烯換算)的丙烯酸系 八I物。加入乙酸乙酯’均勻地混合,從而獲得不揮發成 分3 0 %的黏著劑溶液e。 (雙面黏著帶的調製) 相對於黏著劑溶液£ 1〇〇質量份,添加1.8質量份的曰 本聚胺S曰公司製“ c〇r〇nate L_45”(異氰酸酯系交聯劑,固 30 201037053 15分鐘後’在進行過剝離處理的厚度 布’使乾燥後的厚度為5〇 β m,在8〇 形成黏著劑層。除此之外,藉由與實 體成分45%),攪拌 75 # m的PET膜上塗 C乾燥3分鐘,從而 施例1相同的方法來獲得雙面黏著帶。 對於上述實施例和比較例中使用的發泡體基材、在上 述實施例和比較例中獲得的雙面黏著帶,進行了以下的評 價。將所獲得的結果顯示於表丨〜3。 ΟTo the 100 parts by mass of the above-mentioned adhesive solution A, "C〇ronate L-45" (isocyanate g-based cross-linking agent, solid content 45%) manufactured by a sputum polyurethane company of 1.24 mass was added, and after stirring for 15 minutes, The film was applied to a pet film having a thickness of 75 # m which was subjected to a release treatment, and the thickness after drying was 35 #m, and dried at 80 C for 3 minutes to form an adhesive layer. Next, in a white polyolefin-based foam (thickness: 13 〇 #m, expansion ratio 2.5 times 25% compressive strength, 130 kPa, tensile elastic modulus: 丨14〇n / cm2' tensile strength 14.8 N/cm On both sides of the surface having a surface having a wetting index of 52 mN/m, after laminating each of the above-mentioned adhesive sheets, lamination was carried out using a roller having a linear pressure of 5 kg/cm. Thereafter, at 4 〇. The crucible 48 is thereby obtained as a double-sided adhesive sheet having a thickness of 200 #m. [Examples 2 to 5] In addition to the use of the table. "The battle cell substrate was used instead of the white poly-smoke foam, the thickness of the adhesive after drying was changed", and the text was as shown in Table 1. In addition, by the same method as in Example 1, the double-sided adhesive tape was obtained. [Example 6], and 0.8 mass (isocyanate-based cross-linking was added to remove the adhesion relative to the same method). The solution A 1 was prepared by the Japanese Polyurethane Co., Ltd. as a 'coronate l_45, a solid component (45%), and a double-sided adhesive tape was produced by the same procedure as in the example. [Examples 7 and 8] 25 201037053 Relative to the above adhesive solution (4). By mass, add 2 () f parts: 曰本聚胺醋公司 t "C〇r〇nate "5" (isocyanate vine cross-linking Μ 'solid content 45%) After 15 minutes of mixing, the film was applied to a PET film having a thickness of 75 Å which had been subjected to the release treatment, and the thickness after drying was the thickness shown in Table <>>, and dried at 80T for 3 minutes to form an adhesive layer. In addition to the use of the adhesive layer, the double-sided adhesive tape was obtained by the same method as in Example 。. Further [Example 9] Instead of the white polyolefin-based foam, the black ethylene-vinyl acetate-based foam (thickness: 800 # m, expansion ratio 8 times, 25% compression strength: 34 kPa) tensile strength : 24 8 N / cm, the surface of the surface was corona treated with a wetting index of 52 mN / m), compared with the adhesive solution B 1 〇〇 by mass, 2.0 parts by mass of the Japanese polyurethane company "c〇r〇nate" L_45, (isocyanate-based crosslinking agent, solid content: 45%), and after stirring for 15 minutes, it was applied on a pet film having a thickness of 75 #m which was subjected to a peeling treatment, and the thickness after drying was 50 #m, at 8 ( Rc was dried for 3 minutes to form an adhesive layer. A double-sided adhesive tape was obtained by the same method as in Example 8 except that the adhesive layer was used. [Example 10] (Preparation of Adhesive Solution F) In a reaction vessel of a stirrer, a reflux condenser, a thermometer, a dropping funnel, and a gas inlet port, 85.9 parts by mass of butyl acrylate, 4 parts by mass of acrylic acid, 10 parts by mass of methyl methacrylate, and 4-hydroxybutyl acrylate were used. 0.1 parts by mass, 2, 2 as a polymerization initiator _Azobisisobutyronitrile quality damage solution in a solvent consisting of 1 〇〇 parts by mass of ethyl acetate, at 26 201037053 6 (TC polymerization for 12 hours, thereby obtaining a weight average molecular weight of 7 million (to Polystyrene) In addition, 10 parts by mass of penseldi 6 〇 (pentaerythritol vinegar of polymerized rosin) and 97 parts by mass of cyclohexyl methacrylate were added to 100 parts by mass of the acrylic acid copolymer. Acrylic resin composed of 3 parts by mass of acrylic acid (weight average molecular weight: 6000, glass transition temperature: 66. 〇1 〇 parts by mass, added with ethyl acetate, uniformly mixed, thereby obtaining a non-volatile content of 30% of the adhesive solution F (Preparation of double-sided adhesive tape) 日本·9 parts by mass of Japan Polyurethane Co., Ltd. “C〇ronate L_45” (isocyanate-based crosslinking agent, solid content: 45%) was added to 100 parts by mass of the above-mentioned adhesive solution F. After 15 minutes of soaking, the film was coated on a PET film having a thickness of 75 μm which was subjected to the release treatment, and dried to a thickness of 80 ° C for 3 minutes to form an adhesive layer. A double-sided adhesive tape was obtained by the same method as in Example 1 except for the layer. [Example 11] (Preparation of Adhesive Solution G) t A mixer, a reflux condenser, a thermometer, a dropping funnel, and a nitrogen gas were provided. In the reaction vessel of the inlet, 71.9 parts by mass of butyl acrylate, 2 parts by mass of 2-ethylhexyl acrylate, 5 parts by mass of acrylic acid, 3 parts by mass of methyl acrylate, and 2-hydroxyethyl acrylate. 2,2'-azobisisobutyronitrile as a polymerization initiator (M f parts, dissolved in a solvent composed of ethyl acetate (10) parts by mass (TC polymerization for 12 hours, thereby obtaining a weight average molecular weight of 600,000 (in terms of polystyrene) acrylic copolymer. Then, the amount of the PENSEL D135 (pentaerythritol vinegar of the polymerized rosin) manufactured by Arakawa Chemical Co., Ltd. was added in an amount of 27 parts by weight, and the amount of iodine (10) parts by weight of yasUHARA CHEMICAL Co., Ltd. was added to the acetic acid-based compound. B is brewed, evenly tailed, so as to obtain a non-volatile content of 4S% of the adhesive solution G. (Preparation of double-sided adhesive tape) 曰 聚 聚 聚 Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor Cor After 'mixing for 15 minutes', the film was coated on the film having a thickness of ~m which was subjected to the peeling treatment, and the thickness after drying was made into a core, and dried at 80 C for 3 minutes to form an adhesive layer. Except for this, a double-sided adhesive tape was obtained by the same method as in Example 1. [Comparative Examples 1 and 2] A double-sided adhesive tape was obtained by the same method as in Example 除了 except that the foam base material described in Table 2 was used instead of the white polydextrose foam. [Comparative Example 3] A non-woven fabric (weight per unit area: 17 g/m 2 , tensile strength and IWNAm) was used for the A white poly (four) foaming crucible, except that the dried adhesive having a thickness of 70 / zm was used. A double-sided adhesive sheet was obtained by the same method as in Example i. [Comparative Example 4] A film made of polyethylene terephthalate (PET) was used (thickness: (10), tensile strength: 210 N/cm, and the surface was subjected to corona treatment with a wetting index of 52 mN/m). A double-sided adhesive sheet was obtained by substituting the same method as the one described in the table, in place of the white poly-smoke-type foam, and the thickness after the drying. 28 201037053 [Comparative Example 5] (Preparation of Adhesive Solution C) • In a reaction vessel equipped with a stirrer, a reflux condenser, a thermometer, a dropping funnel, and a nitrogen inlet, butyl acrylate 93.; 54 parts by mass, acetic acid 3 parts by mass of vinyl ester, 2.2 parts by mass of acrylic acid, 1.2 parts by mass of N-vinyl piroxone, 6 parts by mass of 4-hydroxybutyl acrylate, 6 parts by mass, 2,2'-azo two as a polymerization initiator 0.1 parts by mass of isobutyronitrile was dissolved in a solvent composed of 100 parts by mass of ethyl acetate, and polymerized at 60 ° C for 12 hours to obtain a weight average molecular weight of 700,000 (in terms of polystyrene) of acrylic acid. Is a copolymer. Next, 25 parts by mass of Arakawa Chemical SUPER ESTER A 100 was added as an adhesion-imparting resin to 100 parts by mass of the acrylic copolymer, and ethyl acetate was added thereto to uniformly mix to obtain an adhesive solution C having a nonvolatile content of 40%. . (Preparation of double-sided adhesive tape) "Coronate L-45" (isocyanate-based cross-linking agent, solid content 45%) of Japan Polyurethane Co., Ltd. was added in an amount of 1 part by mass to 1 part by mass of the above-mentioned adhesive solution C 1 part by mass. After stirring for 15 minutes, the film was applied on a PET film having a thickness of 75 # m which was subjected to a release treatment, and the thickness after drying was dried at 80 ° C for 3 minutes to form an adhesive layer. Except for this, a double-sided adhesive tape was obtained by the same method as in Example 1. "Comparative Example 6] (Preparation of Adhesive Solution D) In a reaction vessel equipped with a shattering machine, reflux condensation, crying, and w translation | (in the current congee, thermometer, dropping funnel, and nitrogen inlet) 97 parts by mass of butyl acrylate, 2_G parts by mass of acrylic acid, acrylic acid 4, butyl ketone 0, Q1 f parts, 2,2,-azobisisobutyronitrile as polymerization initiator 29 201037053 The 质量" mass part was dissolved in a solvent composed of 1 part by mass of ethyl acetate, and polymerized at 701 for 12 hours to obtain an acrylic copolymer having a weight average molecular weight of 80,000 (in terms of polystyrene). Next, ethyl acetate was added and uniformly mixed to obtain an adhesive solution d having a nonvolatile content of 30%. (Preparation of double-sided adhesive tape) 2.5 parts by mass based on the mass part of the adhesive solution D 1 〇〇 "Cor〇nate L_45" (isocyanate-based cross-linking agent, solid-forming knife 45/6) manufactured by 曰 聚 polyurethane, and after stirring for 15 minutes, it was coated on a PET film having a thickness of 75/zm which was subjected to a peeling treatment, and dried. The thickness is 5〇#m, and it is dried at 8〇C for 3 minutes to form an adhesive layer. Except for this, a double-sided adhesive tape was obtained by the same method as Example i. [Comparative Example 7] (Preparation of Adhesive Solution E) A stirrer, a reflux condenser, a thermometer, a dropping funnel, and a nitrogen gas introduction were provided. In the reaction vessel of the mouth, 98 parts by mass of 2-ethylhexyl acrylate, 1 part by mass of acrylic acid, and 1 part by mass of 4-hydroxybutyl acrylate, 2,2,·azobisisobutyronitrile as a polymerization initiator 0.1 part by mass, dissolved in a solvent consisting of 100 parts of toluene acetate, and polymerized at 701 for 12 hours to obtain an acrylic octahydrate having a reset average molecular weight of 800,000 (in terms of polystyrene). Adding ethyl acetate 'evenly, to obtain a non-volatile component of 30% of the adhesive solution e. (Preparation of double-sided adhesive tape) Adding 1.8 parts by mass of the mass of the adhesive solution Polyamine S曰 company "c〇r〇nate L_45" (isocyanate crosslinking agent, solid 30 201037053 after 15 minutes 'on the thickness of the cloth after the peeling treatment' to make the thickness after drying is 5 〇β m, at 8 〇 form an adhesive layer. In addition, borrow The double-sided adhesive tape was obtained by the same method as in Example 1 by applying C on a PET film stirred with a solid content of 45%) and stirring for 75 minutes for the foam film of the above-mentioned Examples and Comparative Examples. The double-sided adhesive tapes obtained in the above examples and comparative examples were evaluated as follows. The obtained results are shown in Tables 33.

〔發泡體基材和雙面黏著帶的厚度〕 猎由尾崎製作#制、生A 士[The thickness of the foam substrate and the double-sided adhesive tape] Hunted by Ozaki made #制,生A士士

所氣:^的錶盤式厚度計(DIAL THICKNESS GAUGES、「剂、仓…I — )G孓進仃測疋。在雙面黏著帶的情況 下,在剥離掉剝離臈之後進行測定。 〔發泡體基材的層間強度〕 相對於黏著劑溶液cl〇〇質量份,添加u質量份的曰 本聚胺_製“CoronateL_45”(異氰酸醋系交聯劑,固 體成分45%) ’授拌15分鐘後,在進行過剝離處理的厚度 乃/zm的PET膜上塗布,使乾燥後的厚度為心爪,在8〇 乾燥3分鐘,從而形成黏著劑層。接著,在要評價層間 強度的發泡體的雙面上’貼合各1張前述黏著劑層之後, 採用線C 5kgf/em的親進行層壓。其後,在4代熟化々a 小時,製成層間強度測定用的雙面黏著帶。 ^接者,將—側黏著面内襯有厚度25 # m的聚對苯二甲 酸乙二醇酉旨膜之2cm寬且1〇咖長(發泡體基材的流動方向) 輕面勘著帶試樣,在23t · 5G%RH的環境下,用叫的 親在不銹鋼板上進行丨個來回的加壓貼附,在飢放置Μ J夺在23 C放置24小時後,測定··在23<>c · 5〇%rh的 31 201037053 環境下,以300mm/min的拉伸速度,在9〇度方向上,將 發泡體撕裂(損壞基材)時的強度(N/ cm)。 〔拉伸彈性模數、拉伸強度〕 將加工成為標線間隔2cm(發泡體基材的流動方向)、寬 度1cm的試驗片的發泡體基材或雙面黏接薄片(剝離掉剝離 膜),以3〇〇mm/min的拉伸速度拉伸至切斷 中的最大強度。 〔發泡體基材的流動方向和寬度方向的平均氣泡直徑〕 :發泡體基材在寬度方向、流動方向皆切斷為_,用 二=:鏡(,曰立製作所製,S',將所切斷 的發泡體基材的切斷面中央邱 某材的…… 刀放大5〇倍之後,對發泡體 土材的見度方向或流動方向的斷面進行拍照 材的切斷面在該基材厚度方向 ,—土 U ^ . 的 P長度上都被容納於昭 片中:在所獲得的照片中,測定出流動方向或寬^ 放大刖的實際長度為2mm —又° ^ 刀的切斷面令所存在的全部的 -泡直徑,根據其平均值來算出平均氣泡直徑。 ,〔發泡體基材的厚度方向的平均氣泡直徑〕 測定由SEM進行拍照的發 體基材的流動方向的平Μ 土㈣度’在與發泡 了_拍,昭。在所獲:1輕測定相同的條件下進行 '·、、在所獲仔的照片中,藉出a、曰Α , 體基材的任意的地方所存在 數出發泡 式,“厚度方向的平均氣=方向的氣泡數’根據下 個直⑽―趙基材的厚度 32 201037053 將其平均值作為厚度方 在任思的3處對其進行測定, 向的平均氣泡直徑。 〔面黏接強度1〕 1) 在23t,將寬度5mm且長戶〇技μ 食度4cm的2張雙面黏著帶 平行地貼㈣厚度2mm丨5em見方的丙稀酸板(三菱麗陽 ⑻製造的ACRYUTEMR2()()(商標名),色相:透明)。The gas thickness of the dial: (DIAL THICKNESS GAUGES, "agent, warehouse...I — ) G 孓 仃 疋. In the case of double-sided adhesive tape, the measurement is carried out after peeling off the peeling 臈. The interlaminar strength of the bulk substrate is added to the mass fraction of the adhesive solution in an amount of u by mass of the sulfonate polyamine _ "Coronate L_45" (isocyanate vinegar cross-linking agent, solid content 45%) After 15 minutes, the film was coated on a PET film having a thickness of /zm which was subjected to the release treatment, and the thickness after drying was a claw, and dried at 8 Torr for 3 minutes to form an adhesive layer. Next, the interlayer strength was evaluated. After bonding each of the above-mentioned adhesive layers on both sides of the foam, lamination was carried out by using a line C 5 kgf/em. Thereafter, the aging was performed for 4 hours in the 4th generation to prepare a double layer for measuring the interlayer strength. Adhesive tape. ^, the side-adhesive surface is lined with a thickness of 25 # m of polyethylene terephthalate film 2cm wide and 1 〇 coffee length (the flow direction of the foam substrate) Lightly surveyed with a sample, in the environment of 23t · 5G% RH, use the called pro on the stainless steel plate The pressure is applied back to the hunger, and after being placed in the 23 C for 24 hours, the measurement is carried out at a tensile speed of 300 mm/min in the environment of 23 <>c · 5〇%rh 31 201037053, Strength (N/cm) when the foam is torn (damaged to the substrate) in the direction of 9 twist. [Tensile modulus, tensile strength] The processing is made into a line spacing of 2 cm (foam base) The flow direction of the material), the foam substrate of the test piece having a width of 1 cm or the double-sided adhesive sheet (peeling off the release film), and stretching at a tensile speed of 3 〇〇mm/min to the maximum strength during cutting [Average bubble diameter in the flow direction and the width direction of the foam base material]: The foam base material is cut in the width direction and the flow direction, and the second is: mirror (manufactured by 曰立制制, S' After the knives of the cut surface of the cut foam substrate are enlarged by 5 times, the cross section of the foam material is cut in the visibility direction or the flow direction. The section is in the thickness direction of the substrate, and the length of the soil U ^ . is accommodated in the projection: in the obtained photograph, the flow direction is measured or ^ The actual length of the magnified 刖 is 2mm - and ° ^ The cut surface of the knives is the total bubble diameter present, and the average bubble diameter is calculated from the average value. [The average bubble in the thickness direction of the foam substrate Diameter] The flat soil (four degrees) of the flow direction of the hair base material photographed by the SEM was measured, and the foaming was performed, and the same conditions were obtained: In the photo taken, a number of foaming patterns are present in any place where a, 曰Α, and the body substrate are borrowed, and the "average gas in the thickness direction = the number of bubbles in the direction" is based on the thickness of the next straight (10) - Zhao substrate 32 201037053 The average value of the average bubble diameter was measured by taking the average value as the thickness at three places of Rensi. [Face bonding strength 1] 1) At 23t, two double-sided adhesive tapes with a width of 5mm and a long household skill of 4cm are placed in parallel (4) Aluminium plate with a thickness of 2mm丨5em square (Mitsubishi Liyang (8) Manufactured ACRYUTEMR2()() (trade name), hue: transparent).

2) 接著,將由υ製成的附有雙面黏著帶的丙稀酸板, 貼附於:中心部具有直徑lem的孔之厚度2随、腕5咖 的長方形的ABS板(Takiron公司製,色相:自然色,無敵 紋)’使丙稀酸板的中心與ABS板时心—致,用2kg親進 行1個來回的加壓之後,在23t放置i小時作為試驗片。 3) 從試驗片的ABS側藉由細板的孔,採用安裝有直 徑8mm的不錄鋼製探針的拉伸試驗機,以對丙 烯酸板進行按壓,敎出剝離丙稀酸板的強度。 〔面黏接強度2〕 1) 將雙面黏著帶切斷成2咖見方之後,貼⑽於厚度2_ 且2cm見方的丙烯酸板。 2) 將附有雙面黏接薄片的丙烯酸板,貼附於:中心部具 有直仫1Cm的孔、厚度2mm且4cm見方的聚醯胺板(三菱 ^程塑膠(股)製造的Reny (商標名),添加玻璃纖 )吏丙稀k板的中心部和聚醯胺板的中心部一致,用2kg 的輥進仃1個來回的加壓之後,在23艽放置Μ小時,作為 試驗片。 )將°式驗片設置於外形為4cm見方、高度3 cm、厚度 m的不銹鋼製台座上,並使聚醯胺側朝上。 33 201037053 4) 藉由聚酿胺側的孔,朝向丙稀酸板,使前端具有❹ 5簡、長度1Cm的突起的重量1〇〇§的黃銅製圓雖從⑽爪 起以H)Cm間隔連續落下(每i階段3次),敎:能夠在試 驗片確認出膠帶剝離或損壞時的高度。在此,纟高度 的試驗後的試驗片沒有膠帶剝離、損壞時,就此結束&amp;試驗, 記為 “ 686〈”。2) Next, an acrylic plate with a double-sided adhesive tape made of enamel is attached to a rectangular ABS plate having a diameter of lem at the center and a rectangular ABS plate (manufactured by Takiron Co., Ltd., Hue: natural color, invincible pattern) 'The center of the acrylic plate and the ABS plate are the same, and after 1 kg of pressurization with 2 kg, the test piece is placed at 23t for 1 hour. 3) From the ABS side of the test piece, the acrylic plate was pressed by a tensile tester equipped with a stainless steel probe having a diameter of 8 mm by the hole of the thin plate, and the strength of the acrylic plate was peeled off. [Face bond strength 2] 1) After cutting the double-sided adhesive tape into 2 coffee squares, attach (10) the acrylic plate having a thickness of 2 mm and 2 cm square. 2) Attach the acrylic plate with the double-sided adhesive sheet to the Reny (trademark) manufactured by Mitsubishi Chemicals Co., Ltd. with a hole of 1 cm in the center and a thickness of 2 mm and 4 cm square. Name), glass fiber was added) The center of the acryl plate was the same as the center of the polyamide plate, and it was pressurized with a 2 kg roller and then placed at 23 Μ for a test piece. The ° test piece was placed on a stainless steel pedestal having a shape of 4 cm square, a height of 3 cm, and a thickness m, and the polyamine side was turned upward. 33 201037053 4) With the hole on the side of the polyamide, facing the acrylic plate, the front end has a weight of ❹ 5 and a length of 1 cm. The diameter of the brass is 间隔 § § § § § § § § § § § § § § § § § § § § § § § § § § § § Continuously falling (3 times per i stage), 敎: The height at which the tape can be peeled off or damaged can be confirmed on the test piece. Here, when the test piece after the test of the height of the flaw was not peeled off by the tape or damaged, the test was ended and it was recorded as "686 <".

5) 根據測定結果來算出落下能量mJ(=9 8χ高度㈣X 100g)。 〔再加工適合性〕 υ將雙面黏著帶製成外形65mmx43mm、寬度2_的框 架狀樣品,貼附於:厚唐2mm B &amp; π 7 序沒2mm且外形65mmx45mm的丙烯 酸板(三菱麗陽(股)ACRYLITE MR200 (商標名),色相: 透明,下同)。接著,貼附於:厚度2mm且夕卜形9〇mmx5〇mm 的ABS板(丁akiron公司製,色相:自然色,無敏紋,下同), 以2kg的輥進行i個來回的加壓之後,在23。〇放置24小時, 作為試驗片。 2) 對試驗片,在23°C下,向垂直方向剝離丙烯酸板, 評價此時膠帶的狀態。 3) 接著’對殘留於ABS或丙烯酸板上的雙面黏著帶, 用手向剝離角度約135度方向剝離,評價此時的剝離容易 度。 ◎:無基材的層間裂痕且無糊殘留地剝除。 〇:雖然發泡體基材在層間破裂,但其後用手拉所殘 留的雙面黏著帶時,可無糊殘留地剝除。 x:被黏體上殘留了糊。或發泡體基材在層間破裂,其 34 201037053 後即使用手拉所殘留的雙面黏著帶,亦無法剝除。 〔再剝離性〕5) Calculate the drop energy mJ (= 9 8 χ height (4) X 100 g) based on the measurement result. [Reprocessing suitability] υThe double-sided adhesive tape is made into a frame-shaped sample with a shape of 65 mm x 43 mm and a width of 2 mm, attached to: thick Tang 2 mm B &amp; π 7 sequence 2 mm and shape 65 mm x 45 mm acrylic plate (Mitsubishi Riyang (share) ACRYLITE MR200 (trade name), Hue: transparent, the same below). Next, it was attached to an ABS board having a thickness of 2 mm and a shape of 9 mm x 5 mm, which was made by Ding Akron Co., Ltd., hue: natural color, no sensitive pattern, the same below, and was pressed back and forth with 2 kg of rolls. After that, at 23. The crucible was left for 24 hours as a test piece. 2) For the test piece, the acrylic plate was peeled off in the vertical direction at 23 ° C, and the state of the tape at this time was evaluated. 3) Next, the double-sided adhesive tape remaining on the ABS or acrylic plate was peeled off by a hand at a peeling angle of about 135 degrees, and the ease of peeling at this time was evaluated. ◎: There was no interlaminar crack in the substrate and it was peeled off without a paste residue. 〇: Although the foam substrate is ruptured between the layers, the double-sided adhesive tape remaining after the hand can be peeled off without any residue. x: The paste remains on the adherend. Or the foam substrate is ruptured between the layers, and after the use of the double-sided adhesive tape which is left by hand, it cannot be peeled off. [re-peelability]

1)將雙面黏著帶製成為外形65mmx43mm,寬度2麵的 框架狀樣品,貼附於:厚度2mm且外形65mmx45mm的丙 稀酸板。接著,貼附於厚度2_且外形9〇mmx5〇mm的aBS 板,以2kg的輥進行i個來回的加壓之後,在它放置24 小時。 2) 接著,在60。〇 · 9〇%RH的環境下放置7日後,置於 23 C · 50% RH的環境下,作為試驗片。 3) 對忒驗片,在23C下,向垂直方向剝離丙烯酸板, 評價此時膠帶的狀態。 4) 接著,對殘留於ABS或丙烯酸板上的雙面黏著帶, 用手向剝離角度約135度方向剝離,評價此時的剝離容易 度。 ◎.無發泡體基材的層間裂痕,其後無糊殘留地剝除。 〕〇·雖然發泡體基材在層間破裂,但其後用手拉所殘 留的雙面黏著帶時,可無糊殘留地剝除。 X :被黏體上殘留了糊。或發泡體基材在層間破裂,其 後即使用手拉所殘留的雙面黏著帶亦無法剝除。 〔跟隨性試驗〕 Ό將雙面黏著帶切斷為寬度lcm且長度5cm,貼附於厚 度2mm且寬度2cmx長度5cm的丙烯酸板的寬度方向的中 央部’製成附有雙面黏著帶的丙烯酸板。(圖υ。 2)接著,將厚度20 # m的寬度5mm且長度2cm的聚對 苯二曱酸乙二醇酯基材的黏著帶2張,在寬度方向上以km 35 201037053 間隔平行地貼附於另-張厚度2mm的寬度2cmx5cm的丙烯 酸板的中央部,製成附帶高低差的丙烯酸板(圖2)。 )在3C下將附有雙面黏著帶的丙烯酸板裝載於附 帶高低差的丙烯酸板的黏著帶部分之後,肖2kg的親從端 部進行1個來回的加壓(圖3)。 4)從附帶高低差的丙烯酸板側,藉由目視來評價:在高 低差附近的雙面黏著帶的跟隨狀態。 〇.雙面黏著帶密合於附帶高低差的丙烯酸板上。 X·又面黏t帶在高低差附近並無密纟於附帶高低差的 丙烯酸板上。 〔防水性試驗1〕 )將又面黏著帶製成為外形65mmx45mm且寬度2mm 的框架狀樣口口,貼附於厚度2簡且外形。顏⑷腿的丙1) A double-sided adhesive tape was formed into a frame-shaped sample having a shape of 65 mm x 43 mm and a width of 2 faces, and attached to an acrylic plate having a thickness of 2 mm and a shape of 65 mm x 45 mm. Next, an aBS plate having a thickness of 2 mm and a shape of 9 mmx5 mm was attached, and after pressing back and forth with 2 kg of rolls, it was left for 24 hours. 2) Next, at 60. 〇 · After being placed in an environment of 9〇% RH for 7 days, it was placed in a 23 C · 50% RH environment as a test piece. 3) For the test piece, at 23 C, the acrylic plate was peeled off in the vertical direction, and the state of the tape at this time was evaluated. 4) Next, the double-sided adhesive tape remaining on the ABS or acrylic plate was peeled off by a hand at a peeling angle of about 135 degrees, and the ease of peeling at this time was evaluated. ◎. Interlayer cracks in the non-foamed substrate, which were subsequently peeled off without paste residue. 〕 · Although the foam substrate is ruptured between the layers, it can be peeled off without any residue when the double-sided adhesive tape remaining after the hand is left by hand. X: The paste remains on the adherend. Alternatively, the foam substrate may be ruptured between the layers, and thereafter, the double-sided adhesive tape remaining by hand may not be peeled off. [Follow-up test] 双面 The double-sided adhesive tape was cut into a width of 1 cm and a length of 5 cm, and attached to a central portion in the width direction of an acrylic plate having a thickness of 2 mm and a width of 2 cm x a length of 5 cm to make an acrylic having a double-sided adhesive tape. board. (Fig. 2) Next, two adhesive tapes of a polyethylene terephthalate substrate having a thickness of 20 mm and a length of 2 mm and a length of 2 cm were attached in parallel in the width direction at intervals of km 35 201037053 Attached to the center portion of an acrylic plate having a thickness of 2 mm and a width of 2 cm x 5 cm, an acrylic plate with a height difference was formed (Fig. 2). After the acrylic plate with the double-sided adhesive tape was placed on the adhesive tape portion of the acrylic plate with the high and low difference at 3 C, the back of the 2 kg was subjected to one press-back (Fig. 3). 4) From the side of the acrylic plate with the height difference, the following state of the double-sided adhesive tape in the vicinity of the height difference was evaluated by visual observation. 〇. The double-sided adhesive tape is adhered to the acrylic plate with the height difference. The X·refractive t-belt is not close to the height difference, and is not close to the acrylic plate with the height difference. [Water resistance test 1] The rear adhesive tape was formed into a frame-like mouth having a shape of 65 mm x 45 mm and a width of 2 mm, and was attached to the thickness 2 in a simple shape. Yan (4) leg of C

板之後貼附於厚度2mm且外形65mmx45mm的ABS 板以2kg的輥進行1個來回的加壓之後,在23°c放置24 小時’作為試驗片。 2)對試驗片’實施在抑的5 f量%表面活性劑溶液 (用自來水稀釋P&amp;G公司製J〇Y而製成)中浸潰分鐘— 取出放置10分鐘的循環3〇次之後,評價再次浸潰於溶液 時框架内有無浸水。 〇.無浸水 x .有浸水 〔防水性試驗2〕 )冬又面黏著▼製成為外形65mmx45mm且寬度2mm ’、爿、樣°°貼附於厚度2mm且外形65mmx45mm的丙 36 201037053After the plate was attached to an ABS plate having a thickness of 2 mm and a shape of 65 mm x 45 mm, one back pressure was applied with a 2 kg roller, and then placed at 23 ° C for 24 hours as a test piece. 2) After immersing the test piece in a 5 f amount % surfactant solution (made by tapping water and making J 〇 Y manufactured by G), the test piece was taken out for 3 minutes after being placed for 10 minutes. Evaluate whether there is any immersion in the frame when the solution is again immersed in the solution. 〇. No immersion water x. Immersion water [water resistance test 2]) Winter surface adhesion ▼ made into a shape of 65mmx45mm and a width of 2mm ‘, 爿, sample °° attached to a thickness of 2mm and a shape of 65mmx45mm C 36 201037053

烯酸板之後,貼附於厚度2mm且外形15〇1111^1〇〇111111的ABS 板的中央部(圖4)。用2kg的輥進行i個來回的加壓之後, 在23 C玫置24小時,作為試驗片。 2) 在23 C下’在杜邦式衝擊試驗機(TESTER產業股份 有限公司製)的台座上設置長度15〇mm、寬度1〇〇mm、高度 5mm的U ( π )子型測定台(厚度的铭製物),在其上 裝載試驗片並使丙烯酸板朝下(圖5)。從abs板側,使直徑 0 25ηΐΐη且貝量300g的不銹鋼製擊芯從高度3〇cm位置落下, 以10秒間隔施加5次的對ABS板的中心部分的衝擊(圖6)。 在此,鈿加衝擊而丙烯酸板發生脫落時,就此結束試驗。 3) 對實施過衝擊的試驗片,實施在23。〇的5質量%表 面活〖生劑/谷液(用自來水稀釋p &amp; G公司製而製成)浸 /貝10分鐘—取出放置1〇分鐘的循環3〇次之後,評價再次 浸潰於溶液時框架内有無浸水。 ◎:無浸水,發泡體的外觀沒有變化。 〇 〇.雖然無浸水,但確認出發泡體層的一部分有微少 的裂傷。 X .有次水,或在落下衝擊的階段丙烯酸板就發生了脫 落。 〔氣密性試驗] 。1)將雙面黏著帶製成為外形5cmx4cm且寬度的框 架狀樣品,貼附於厚度2mm且外形5Cmx5cm、在中央具有 直&amp; 3mm的孔的開孔丙烯酸板之後,貼附於厚度且外 形7Cmx5Cm的長方形的丙烯酸板的中央部(圖乃。用的 挺進行1個來回的加壓之後,纟23t放置24小時,作為試 37 201037053 驗片。 2) 在23°C,從開孔丙烯酸板,用氮氣施加〇.〇2MPa的 壓力(圖8)。 3) 測定直到氮氣從窗框狀膠帶部分洩漏的時間。 表1 實施例1 實施例2 實施例3 實施例4 實施例5 實施例6 實施例7 實施例8 實施例9 粘 種類 A A A A A A B B A 著 塗布厚度|&gt;m] 35 35 35 50 50 35 35 50 70 劑 凝膠分率[%] 46 46 46 46 46 33 46 46 46 Tan &lt;5極大值溫度[°C] -11 -11 -11 -11 -11 -11 -Ί -7 -11 白色聚 黑色聚 白色聚 白色聚 黑色聚 白色聚 白色聚 黑色 黑色聚 mm 烯烴系 烯烴系 烯烴系 烯烴系 烯烴系 烯烴系 烯烴系 EVA系 烯烴系 厚度[#ηι] 130 130 100 300 500 130 130 800 200 25%壓縮強度[kPa] 130 150 110 92 98 130 130 34 34 基 層間強度[N/cm] 18.0 20.0 12.8 23.0 15.0 18.0 18.0 33.6 15.0 材 拉伸彈性模數[N/cm2] 1140 1200 1080 510 250 1140 1140 310 520 拉伸強度[N/cm] 14.8 15.0 10.8 15.3 12.5 14.8 14.8 24.8 10.0 平均氣 厚度方向 25 30 30 75 63 25 25 100 50 泡直徑 流動方向 210 130 137 136 302 210 210 320 400 (#m) 寬度方向 273 168 178 180 376 273 273 150 630 發泡位率[倍] 2.5 2.5 2.7 5 10 2.5 2.5 8.0 5 厚度[//m] 200 200 150 400 600 200 200 900 340 Tan &lt;5極大值溫度[°C] -1 -1 -1 -3 -2 -1 5 5 -1 雙 丁汪115極大值[-] 0.74 0.74 0.74 0.80 0.55 0.74 0.73 0.45 0.64 面 面接著強度l[N/4cm2] 150 155 140 180 170 150 130 130 160 面接著強度2[mJ] 490 588 392 588 686 490 490 686&lt; 392 再加工適合性 ◎ ◎ ◎ ◎ ◎ ◎ 〇 ◎ 〇 著 再剝離性 ◎ ◎ 〇 ◎ ◎ 〇 〇 〇 〇 帶 跟隨性試驗 〇 〇 〇 〇 〇 〇 〇 〇 〇 防水性試驗1 〇 〇 〇 〇 〇 〇 〇 〇 〇 防水性試驗2 ◎ ◎ 〇 ◎ ◎ ◎ ◎ ◎ 〇 38 201037053After the olefin plate, it was attached to the center of the ABS plate having a thickness of 2 mm and an outer shape of 15〇1111^1〇〇111111 (Fig. 4). After pressurizing i back and forth with a 2 kg roller, it was placed at 23 C for 24 hours to serve as a test piece. 2) At 23 C, a U (π) subtype measuring table with a length of 15 mm, a width of 1 mm, and a height of 5 mm is set on the pedestal of the DuPont-type impact tester (manufactured by TESTER Industries Co., Ltd.) (thickness Ingredient), on which the test piece is loaded with the acrylic plate facing down (Fig. 5). From the side of the abs plate, a stainless steel shot core having a diameter of 0 25 η ΐΐ and a volume of 300 g was dropped from a height of 3 〇 cm, and impact on the central portion of the ABS plate was applied five times at intervals of 10 seconds (Fig. 6). Here, when the impact is applied and the acrylic sheet falls off, the test is terminated. 3) The test piece that has been subjected to the impact is implemented at 23. 5% by mass of surface 〖 生 / / / 生 生 生 生 生 生 生 生 生 生 生 生 生 生 生 生 生 生 生 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 Whether there is water immersion in the frame during the solution. ◎: There was no water immersion, and the appearance of the foam did not change. 〇 〇. Although there is no water immersion, it is confirmed that a part of the foam layer has a slight laceration. X. There is water, or the acrylic plate is detached at the stage of the impact. [Air tightness test]. 1) The double-sided adhesive tape was formed into a frame-like sample having a shape of 5 cm x 4 cm in width and attached to an open-cell acrylic plate having a thickness of 2 mm and a shape of 5 cm x 5 cm and having a straight &amp; 3 mm hole in the center, attached to the thickness and having a shape of 7 cmx5 cm. The center of the rectangular acrylic plate (Fig. is used after a press of 1 back and forth, 纟 23t placed for 24 hours, as test 37 201037053. 2) At 23 ° C, from the open hole acrylic plate, A pressure of MPa 2 MPa was applied with nitrogen (Fig. 8). 3) Determine the time until nitrogen leaks from the sash-like tape portion. Table 1 Example 1 Example 2 Example 3 Example 4 Example 5 Example 6 Example 7 Example 8 Example 9 Adhesive type AAAAAABBA Coating thickness|&gt;m] 35 35 35 50 50 35 35 50 70 Gel fraction [%] 46 46 46 46 46 33 46 46 46 Tan &lt;5maximum temperature [°C] -11 -11 -11 -11 -11 -11 -Ί -7 -11 White poly black poly white Poly white poly black poly white poly white poly black black poly mm olefin olefin olefin olefin olefin olefin olefin EVA olefin system thickness [# ηι] 130 130 100 300 500 130 130 800 200 25% compressive strength [ kPa] 130 150 110 92 98 130 130 34 34 Inter-base strength [N/cm] 18.0 20.0 12.8 23.0 15.0 18.0 18.0 33.6 15.0 Material tensile modulus [N/cm2] 1140 1200 1080 510 250 1140 1140 310 520 Stretching Strength [N/cm] 14.8 15.0 10.8 15.3 12.5 14.8 14.8 24.8 10.0 Average gas thickness direction 25 30 30 75 63 25 25 100 50 Bubble diameter Flow direction 210 130 137 136 302 210 210 320 400 (#m) Width direction 273 168 178 180 376 273 273 150 630 Foaming rate [times] 2.5 2.5 2.7 5 10 2.5 2.5 8.0 5 Thickness [//m] 200 200 150 400 600 200 200 900 340 Tan &lt;5maximum temperature [°C] -1 -1 -1 -3 -2 -1 5 5 -1 Double汪115max[-] 0.74 0.74 0.74 0.80 0.55 0.74 0.73 0.45 0.64 Surface adhesion strength l[N/4cm2] 150 155 140 180 170 150 130 130 160 Surface adhesion strength 2[mJ] 490 588 392 588 686 490 490 686&lt 392 Reprocessing suitability ◎ ◎ ◎ ◎ ◎ ◎ 〇 ◎ 再 再 再 ◎ ◎ ◎ ◎ ◎ 跟随 belt follow-up test 〇〇〇〇〇〇〇〇〇 waterproof test 1 〇〇〇〇〇 〇〇〇〇Water resistance test 2 ◎ ◎ 〇 ◎ ◎ ◎ ◎ ◎ 〇38 201037053

比較例1 比車交例2 比較例3 比較例4 比車交例5 比較例6 比較例7 粘 種類 A A A A A A B 著 塗布厚度[ym] 50 50 70 50 50 35 35 劑 凝膠分率[°/〇] 46 46 46 46 46 33 46 Tan (5極大值溫度[°C] -11 -11 -11 -11 -11 -11 -7 種類 黑色聚 烯烴系 白色聚 烯烴系 不織布 PET 白色聚 烯烴系 白色聚 烯烴系 白色聚 烯烴系 厚度[//m] 100 100 - 100 500 130 130 25%壓縮強度[kPa] 70 190 - - 98 130 130 基 層間強度[N/cm] 10 24.3 - - 18 18 18 材 拉伸彈性模數[N/cm2] 770 1600 - - 1140 1140 1140 拉伸強度[N/cm] 8.0 16.0 16.0 210.0 14.8 14.8 14.8 平均氣 厚度方向 50 20 — — 25 25 25 泡直徑 流動方向 500 209 - - 210 210 210 (μτη) 寬度方向 650 230 - - 273 273 273 發泡位率[倍] 3 2 - - 2.5 2.5 2.5 厚度[^m] 200 200 150 200 200 200 200 Tan 5極大值溫度[°C] -1 -1 -11 -11 -5 -25 -30 雙 面 Tan 5極大值[-] 0.75 0.79 1.77 1.82 0.83 0.86 0.82 面接著強度l[N/4cm2] 140 150 120 140 120 90 34 面接著強度2[mJ] 196 588 294 392 490 294 196 黏 再加工適合性 X ◎ ◎ ◎ X ◎ ◎ 著 再剝離性 X ◎ ◎ ◎ X 〇 ◎ 帶 跟隨性試驗 〇 X X X 〇 X X 防水性試驗1 〇 X X X 〇 X X 防水性試驗2 〇 X X X ◎ X X 39 201037053Comparative Example 1 Example 2 Comparison Example 3 Comparative Example 4 Comparative Example 5 Comparative Example 6 Comparative Example 7 Adhesive Type AAAAAAB Coating Thickness [ym] 50 50 70 50 50 35 35 Gel Fraction [°/〇 ] 46 46 46 46 46 33 46 Tan (5 max. temperature [°C] -11 -11 -11 -11 -11 -11 -7 Black polyolefin white polyolefin non-woven PET white polyolefin white polyolefin White polyolefin thickness [//m] 100 100 - 100 500 130 130 25% compressive strength [kPa] 70 190 - - 98 130 130 Inter-base strength [N/cm] 10 24.3 - - 18 18 18 Material stretching Elastic modulus [N/cm2] 770 1600 - - 1140 1140 1140 Tensile strength [N/cm] 8.0 16.0 16.0 210.0 14.8 14.8 14.8 Average gas thickness direction 50 20 — — 25 25 25 Bubble diameter flow direction 500 209 - - 210 210 210 (μτη) Width direction 650 230 - - 273 273 273 Foaming rate [倍] 3 2 - - 2.5 2.5 2.5 Thickness [^m] 200 200 150 200 200 200 200 Tan 5 Maximum temperature [°C] - 1 -1 -11 -11 -5 -25 -30 Double-sided Tan 5 maxima [-] 0.75 0.79 1.77 1.82 0.83 0.86 0.82 Surface adhesion strength l[N/4cm2] 140 150 12 0 140 120 90 34 Surface adhesion strength 2 [mJ] 196 588 294 392 490 294 196 Adhesive rework suitability X ◎ ◎ ◎ X ◎ ◎ Re-peelability X ◎ ◎ ◎ X 〇 ◎ Belt follow-up test 〇 XXX 〇 XX Water resistance test 1 〇 XXX 〇 XX Water resistance test 2 〇 XXX ◎ XX 39 201037053

實施例10 實施例11 種類 F G 粘 塗布厚度[//m] 35 35 著 凝膠分率[%] 53 40 劑 20°C之儲存彈性模數 [xl05Pa] 4.0 3.2 Tan (5極大值溫度[°C] -3 8 種類 白色聚 烯烴系 白色聚 烯烴系 厚度[Am] 130 130 25%壓縮強度[kPa] 130 130 基 層間強度[N/cm] 18.0 18.0 材 拉伸彈性模數[N/cm2] 1140 1140 拉伸強度[N/cm] 14.8 14.8 平均氣 厚度方向 25 25 泡直徑 流動方向 210 210 (/zm) 寬度方向 273 273 發泡位率[倍] 2.5 2.5 厚度[//m] 200 200 Tan 5極大值溫度[°C] 7 16 Tan 5極大值[-] 0.5 0.66 雙 面接著強度l[N/4cm2] 160 180 面 面接著強度2[mJ] 294 294 黏 再加工適合性 〇 〇 著 再剝離性 〇 〇 帶 跟隨性試驗 〇 〇 防水性試驗1 〇 〇 防水性試驗2 〇 ◎ 氣密性試驗 80分鐘 60分鐘 如從上述實施例1〜9可知,本發明的雙面黏著帶兼具 與被黏體的優異的密合性和再加工適合性、再剝離性。另 外,實施例10〜11的雙面黏著帶,在具有優異的密合性、 40 201037053 #加工適合性的同時,還具有適宜的氣密性。另一方面, . 就比較例1的雙面黏著帶而言,由於發泡體基材的層間強 度拉伸強度低,因此在實用時,在再加工或再剝離時難 乂釗掉雙面黏著帶。另外’就比較例2〜4的雙面黏著帶而 °跟隨性都差,因而在防水性試驗中確認有浸水,難以 實現防水性。就比較例5而言,在再加工和再剝離時,難 、釗離又面黏著帶。就比較例6和7而言,黏接力都低, 難以貫現防水性。 〇 L園武簡單說明】 圖1表示跟隨性試驗用的附有雙面黏著帶的丙稀酸板 的概念圖。 微 圖I不跟隨性試驗用的附帶高低差的丙稀酸板的概 念圖。Example 10 Example 11 Type FG Adhesive coating thickness [//m] 35 35 Gel fraction [%] 53 40 Agent storage elastic modulus at 20 ° C [xl05Pa] 4.0 3.2 Tan (5 max temperature [° C] -3 8 kinds of white polyolefin white polyolefin system thickness [Am] 130 130 25% compressive strength [kPa] 130 130 interlayer strength [N/cm] 18.0 18.0 material tensile modulus of elasticity [N/cm2] 1140 1140 Tensile strength [N/cm] 14.8 14.8 Average gas thickness direction 25 25 Bubble diameter Flow direction 210 210 (/zm) Width direction 273 273 Foaming rate [times] 2.5 2.5 Thickness [//m] 200 200 Tan 5maximum temperature [°C] 7 16 Tan 5 max. [-] 0.5 0.66 double-sided strength l[N/4cm2] 160 180 surface adhesion strength 2[mJ] 294 294 adhesive rework suitability Peeling tape following test 〇〇 Water resistance test 1 〇〇 Water repellency test 2 〇 ◎ Air tightness test 80 minutes 60 minutes As can be seen from the above Examples 1 to 9, the double-sided adhesive tape of the present invention has both Excellent adhesion and reworkability and re-peelability of the adherend. Further, Example 10 11 double-sided adhesive tape, with excellent adhesion, 40 201037053 # processing suitability, but also has a suitable airtightness. On the other hand, in the double-sided adhesive tape of Comparative Example 1, due to Since the interlaminar strength tensile strength of the foam base material is low, it is difficult to remove the double-sided adhesive tape during reworking or re-peeling in practical use. In addition, the double-sided adhesive tape of Comparative Examples 2 to 4 is followed by ° Since the properties were inferior, it was confirmed that water immersion was observed in the water repellency test, and it was difficult to achieve water repellency. In Comparative Example 5, it was difficult to peel off the adhesive tape at the time of reworking and re-peeling, and Comparative Examples 6 and 7 In other words, the adhesion is low, and it is difficult to achieve water resistance. 〇L Yuan Wu simple explanation] Figure 1 shows the conceptual diagram of the acrylic plate with double-sided adhesive tape for follow-up test. Micrograph I non-following test A conceptual diagram of an acrylic plate with a height difference.

G %说“ &lt; 斷面方向’對跟隨性試驗的附有雙面點著帶的 概念圖。Τ间低差的丙烯酸板的貼合狀態進行觀察的 圖4表示防水性試驗2用的試驗片的概念圖。 丙烤酸板朝下的方式將測定台防水性試驗2用 ==Η字形測定台6(厚度一製物) 上的狀悲下,從測定a Α &amp; — _ 、 ° 、底面側進行觀察的概念圖。 圖表不施加落下衝擊的操作的概念圖。 圊7表示氣密性試驗的試驗片的概念圓。 圖8表示向試驗片施加壓力的操作的概念圖。 41 201037053 【主要元件符號說明】 1 雙面黏著帶 2 丙稀酸板 3 高低差用的黏著帶 4 評價跟隨性的部位 5 ABS 板 6 用擊芯撞擊的地方 7 落下衝擊用擊芯 8 U字形測定台 9 開孔丙烯酸板 10 厚度3mm的丙稀酸板 11 氮氣導入管 12 氮氣 42G % says " &lt; section direction" is a conceptual diagram with a double-sided dot tape for the follow-up test. Figure 4 showing the adhesion state of the acrylic plate with a low gap between the turns shows the test for the water resistance test 2 Conceptual diagram of the sheet. The method of measuring the water repellency test 2 of the measuring board with the acrylic acid plate facing downwards is determined by using the == Η-shaped measuring table 6 (thickness of one product), from the measurement a Α &amp; — _ , ° Fig. 8 is a conceptual diagram of an operation of a test piece in which the airtightness test is performed. Fig. 8 is a conceptual diagram showing an operation of applying pressure to the test piece. [Main component symbol description] 1 Double-sided adhesive tape 2 Acrylic acid plate 3 Adhesive tape for height difference 4 Evaluation of follow-up parts 5 ABS plate 6 Place where impact is hit by the core 7 Drop impact core 8 U-shaped measuring table 9 open-cell acrylic plate 10 3 mm thick acrylic plate 11 nitrogen inlet pipe 12 nitrogen 42

Claims (1)

201037053 七、申請專利範圍: Ο 1·一種雙面黏著帶,係在發泡體基材的兩面具有黏著劑 層而得者,其特徵在於,該發泡體基材的層間強度為12N /⑽以上,25%壓縮強度為3〇〜麗以,該黏著劑層係由 丙烯酸系黏著劑組合物所構成’該丙烯酸系黏著劑组合物 係含有丙烯酸系共聚物與聚合松香I系黏著賦予樹脂,該 丙烤酸系共聚物係含有碳原子數為4〜12的(甲基)丙稀酸 酯和具有羧基的乙烯基單體作為單體成分。 2·如申請專利範圍第&quot;員之雙面黏著帶,其中該發泡體 基材的拉伸彈性模數為卿cm2以上’單位寬度的拉伸 強度為1 ON/ cm以上。 利範圍第1或2項之雙面黏著帶,其中該發 =材的厚度方向的平均氣泡直徑為M00 一流動方 向和寬度方向的平均氣泡直徑為J 2〜700“ m ^ 4.如申請專利範圍第3項之雙面黏著 其鉍沾也士 ’、中該發泡體 基材的^動方向的平均氣泡直徑相對於厚度 泡直徑的比為,寬度方向的平 千句乳 度方向的平均氣泡直徑的比為,直後相對於厚 ,5.如申請專利範圍第.…項之雙面黏著帶 泡體基材為聚烯烴系發泡體基材。 、'^發 6·如申請專利範圍第【或2項之雙面黏著帶 於該丙浠酸系共聚⑯100質量份,含有該:中相對 著賦予樹脂1 0〜40質量份。 。权香自曰系黏 7.如申請專利範圍第1或2項之雙面黏著帶,其中’ 稀酸系共聚物係含有分子内具有3級胺骨架的乙 43 201037053 作為單體成分。 8. 如申請專利範圍第 再生或再利用的電子機3項之雙面黏著帶,其用於可 、器的構件的固定。 9. 如申請專利範圍 ^ ^ ^ 弟1或2項之雙面黏著帶’其用 有防水功能的電子機器 、用於具 獨立氣泡形成的發泡體/的固疋,㈣泡體基材為由 广_如申睛專利範圍第!或2項之雙面黏著帶,其中該 黏者劑層在頻率1Ηζ τ的動態黏彈性頻譜中顯示損耗正切 的極大值的溫度為— 3〇〜10°c。 11.如申請專利範圍第1項之雙面黏著帶,其中該雙面 黏著帶在頻率1Η Z下的動態黏彈性頻譜中顯示損耗正切的 極大值的溫度為_3〇〜2〇。(3 ’該損耗正切的極大值為以 下。 八、圖式: (如次頁) 44201037053 VII. Patent application scope: Ο 1. A double-sided adhesive tape having an adhesive layer on both sides of a foam substrate, characterized in that the interlayer strength of the foam substrate is 12N / (10) In the above, the 25% compressive strength is 3 Å to 丽, and the adhesive layer is composed of an acrylic pressure-sensitive adhesive composition. The acrylic pressure-sensitive adhesive composition contains an acrylic copolymer and a polymerized rosin I-based adhesion-providing resin. The acrylic acid-based copolymer contains a (meth) acrylate having 4 to 12 carbon atoms and a vinyl monomer having a carboxyl group as a monomer component. 2. The double-sided adhesive tape of the applicant's patent range, wherein the foam substrate has a tensile modulus of more than cm 2 or more and a tensile strength per unit width of 1 ON/cm or more. The double-sided adhesive tape of item 1 or 2, wherein the average bubble diameter in the thickness direction of the hair material is M00, and the average bubble diameter in the flow direction and the width direction is J 2 to 700" m ^ 4. In the third aspect of the range, the double-sided adhesion is the same as the thickness of the foamed substrate, and the ratio of the average bubble diameter to the thickness of the bubble is the average of the width direction of the longitudinal direction. The ratio of the diameter of the bubble is straight and then relatively thick. 5. The double-sided adhesive tape substrate of the item of the patent application is a polyolefin-based foam substrate. The double-sided adhesive tape of the item [or item 2] is used in the copolymerization of 16100 parts by mass of the propionic acid-based copolymer, and contains: 10 to 40 parts by mass of the resin to be added in the opposite direction. A double-sided adhesive tape of 1 or 2, wherein the 'dilute acid copolymer contains B, 43, 2010, 370, 153, which has a tertiary amine skeleton in the molecule as a monomer component. 8. The electronic machine 3 is regenerated or reused as claimed in the patent application. Double-sided adhesive tape for components of the device 9. If you apply for a patent, ^ ^ ^ Dimensional adhesive tape of 1 or 2, 'Electronic machine with waterproof function, foam for solid bubble formation, (4) Bubble base The material is a double-sided adhesive tape of the broadest _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ 10°c. 11. The double-sided adhesive tape of claim 1, wherein the double-sided adhesive tape exhibits a maximum value of the loss tangent in the dynamic viscoelastic spectrum at a frequency of 1 Η Z is _3〇~2 〇. (3 'The maximum value of the loss tangent is the following. VIII. Schema: (such as the next page) 44
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US10316221B2 (en) 2012-03-22 2019-06-11 Dic Corporation Adhesive tape
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TWI507504B (en) * 2013-05-27 2015-11-11 Dainippon Ink & Chemicals Double-sided adhesive tape
TWI634143B (en) * 2013-09-30 2018-09-01 積水化學工業股份有限公司 Crosslinked polyolefin resin foam sheet
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US10793755B2 (en) 2014-03-13 2020-10-06 Dic Corporation Adhesive sheet and electronic device

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JP5556987B2 (en) 2014-07-23
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