TW201139259A - Adhesive material reel - Google Patents

Adhesive material reel Download PDF

Info

Publication number
TW201139259A
TW201139259A TW100108321A TW100108321A TW201139259A TW 201139259 A TW201139259 A TW 201139259A TW 100108321 A TW100108321 A TW 100108321A TW 100108321 A TW100108321 A TW 100108321A TW 201139259 A TW201139259 A TW 201139259A
Authority
TW
Taiwan
Prior art keywords
adhesive
mass
adhesive layer
substrate
mentioned
Prior art date
Application number
TW100108321A
Other languages
Chinese (zh)
Other versions
TWI435841B (en
Inventor
Kazuya Matsuda
Takashi Seki
Tohru Fujinawa
Tadayasu Fujieda
Original Assignee
Hitachi Chemical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Hitachi Chemical Co Ltd filed Critical Hitachi Chemical Co Ltd
Publication of TW201139259A publication Critical patent/TW201139259A/en
Application granted granted Critical
Publication of TWI435841B publication Critical patent/TWI435841B/en

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01RELECTRICALLY-CONDUCTIVE CONNECTIONS; STRUCTURAL ASSOCIATIONS OF A PLURALITY OF MUTUALLY-INSULATED ELECTRICAL CONNECTING ELEMENTS; COUPLING DEVICES; CURRENT COLLECTORS
    • H01R4/00Electrically-conductive connections between two or more conductive members in direct contact, i.e. touching one another; Means for effecting or maintaining such contact; Electrically-conductive connections having two or more spaced connecting locations for conductors and using contact members penetrating insulation
    • H01R4/04Electrically-conductive connections between two or more conductive members in direct contact, i.e. touching one another; Means for effecting or maintaining such contact; Electrically-conductive connections having two or more spaced connecting locations for conductors and using contact members penetrating insulation using electrically conductive adhesives
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65HHANDLING THIN OR FILAMENTARY MATERIAL, e.g. SHEETS, WEBS, CABLES
    • B65H37/00Article or web delivery apparatus incorporating devices for performing specified auxiliary operations
    • B65H37/002Web delivery apparatus, the web serving as support for articles, material or another web
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J11/00Features of adhesives not provided for in group C09J9/00, e.g. additives
    • C09J11/02Non-macromolecular additives
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J163/00Adhesives based on epoxy resins; Adhesives based on derivatives of epoxy resins
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00Adhesives in the form of films or foils
    • C09J7/30Adhesives in the form of films or foils characterised by the adhesive composition
    • C09J7/35Heat-activated
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J9/00Adhesives characterised by their physical nature or the effects produced, e.g. glue sticks
    • C09J9/02Electrically-conducting adhesives
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B5/00Non-insulated conductors or conductive bodies characterised by their form
    • H01B5/16Non-insulated conductors or conductive bodies characterised by their form comprising conductive material in insulating or poorly conductive material, e.g. conductive rubber
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L24/00Arrangements for connecting or disconnecting semiconductor or solid-state bodies; Methods or apparatus related thereto
    • H01L24/01Means for bonding being attached to, or being formed on, the surface to be connected, e.g. chip-to-package, die-attach, "first-level" interconnects; Manufacturing methods related thereto
    • H01L24/26Layer connectors, e.g. plate connectors, solder or adhesive layers; Manufacturing methods related thereto
    • H01L24/28Structure, shape, material or disposition of the layer connectors prior to the connecting process
    • H01L24/29Structure, shape, material or disposition of the layer connectors prior to the connecting process of an individual layer connector
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2203/00Applications of adhesives in processes or use of adhesives in the form of films or foils
    • C09J2203/326Applications of adhesives in processes or use of adhesives in the form of films or foils for bonding electronic components such as wafers, chips or semiconductors
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2301/00Additional features of adhesives in the form of films or foils
    • C09J2301/30Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier
    • C09J2301/312Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier parameters being the characterizing feature
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2463/00Presence of epoxy resin
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2224/00Indexing scheme for arrangements for connecting or disconnecting semiconductor or solid-state bodies and methods related thereto as covered by H01L24/00
    • H01L2224/73Means for bonding being of different types provided for in two or more of groups H01L2224/10, H01L2224/18, H01L2224/26, H01L2224/34, H01L2224/42, H01L2224/50, H01L2224/63, H01L2224/71
    • H01L2224/732Location after the connecting process
    • H01L2224/73201Location after the connecting process on the same surface
    • H01L2224/73203Bump and layer connectors
    • H01L2224/73204Bump and layer connectors the bump connector being embedded into the layer connector
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2224/00Indexing scheme for arrangements for connecting or disconnecting semiconductor or solid-state bodies and methods related thereto as covered by H01L24/00
    • H01L2224/80Methods for connecting semiconductor or other solid state bodies using means for bonding being attached to, or being formed on, the surface to be connected
    • H01L2224/83Methods for connecting semiconductor or other solid state bodies using means for bonding being attached to, or being formed on, the surface to be connected using a layer connector
    • H01L2224/831Methods for connecting semiconductor or other solid state bodies using means for bonding being attached to, or being formed on, the surface to be connected using a layer connector the layer connector being supplied to the parts to be connected in the bonding apparatus
    • H01L2224/83101Methods for connecting semiconductor or other solid state bodies using means for bonding being attached to, or being formed on, the surface to be connected using a layer connector the layer connector being supplied to the parts to be connected in the bonding apparatus as prepeg comprising a layer connector, e.g. provided in an insulating plate member
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2924/00Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
    • H01L2924/15Details of package parts other than the semiconductor or other solid state devices to be connected
    • H01L2924/151Die mounting substrate
    • H01L2924/156Material
    • H01L2924/15786Material with a principal constituent of the material being a non metallic, non metalloid inorganic material
    • H01L2924/15788Glasses, e.g. amorphous oxides, nitrides or fluorides

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Computer Hardware Design (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Power Engineering (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Adhesive Tapes (AREA)
  • Storage Of Web-Like Or Filamentary Materials (AREA)

Abstract

An adhesive material reel of this invention includes: a reel core, a pair of side plates disposed on the both side of the reel core and opposite to each other, an adhesive material tape having a tape-shaped substrate and an adhesive layer disposed on one side of the substrate, wherein the adhesive material tape is wrapped on the reel core in a way of the side of the substrate which the adhesive layer is not formed thereon facing the reel core.

Description

201139259 L 六、發明說明: 【發明所屬之技術領域】 本發明是有關於-種接著材捲筒,更詳細而言是有關 於-種具有帶狀基材及設置於該基材的—面上的接著劑層 的接著材帶捲繞於捲芯上的接著材捲筒。 【先前技術】 用以將具有多個電極的電路構件彼此電性連接來製造 電路連接體的連接材料是使用異向導電膜(An—。 Conductive Film ’ ACF)。異向導電膜是於印刷配線基板、 液晶顯示器(Liquid Crystal Display,LCD )用玻璃基板、 可撓性印刷基板等基板上連接積體電路(201139259 L VI. OBJECTS OF THE INVENTION: TECHNICAL FIELD OF THE INVENTION The present invention relates to a roll of a composite material, and more particularly to a tape-shaped substrate and a surface disposed on the substrate The adhesive tape of the adhesive layer is wound around a web of reel on the core. [Prior Art] A connecting material for electrically connecting circuit members having a plurality of electrodes to each other to manufacture a circuit connecting body is an anisotropic conductive film (ACF). The anisotropic conductive film is an integrated circuit connected to a substrate such as a printed wiring board, a liquid crystal display (LCD) glass substrate, or a flexible printed circuit board (

Circuit,IC )、大型積體電路(Scde integratedCircuit, IC), large integrated circuit (Scde integrated

Circuit,LSI)料導體元件或封裝料構件時,以保持相 對的電極彼此的導通狀態,且保持鄰接的電極彼此的絕緣 的方式進行電性連接及機械固著的連接材料。除異向導電 膜以外’已知非導電膜(Non-Conductive Film,NCF)等 連接材料。 上述連接材料包含含有熱硬化性樹脂的接著劑成分、 及根據異向導電膜的情況而視需要調配的導電粒子,於聚 對苯一甲酸乙二酯膜(Polyethylene terephthalate film,PET 膜)等基材上形成膜狀。將所得膜的整幅材料以成為適合 於用途的寬度的方式切斷為帶狀,並將其纏繞於捲芯上而 製造接著材捲筒(參照專利文獻1)。 但是,使電路連接體的連接可靠性下降的原因之一有 201139259 稱為結塊的現象。結塊是指當將捲繞狀態的接著材帶拉出 而使用時’接著劑層轉印於基材的背面的現象。設置於基 材的一面的接著劑層為未硬化狀態’因此具有某種程度的 流動性。若將接著材捲筒長時間放置,則存在接著劑自接 著材帶的端面滲出,且該接著劑黏接著於捲筒的側板上的 情況。若於該狀態下將接著材帶自捲筒上拉出,則存在產 生接著劑層的一部分轉印於基材的背面的不良狀態、或接 著劑層自基材上剝離而僅拉出基材的不良狀態的情況。 圖9是示意地表示自先前的接著材捲筒上拉出接著材 帶時所產生的結塊的一例的剖面圖。圖9所示的接著材帶 25是以接著劑層28朝向捲芯侧(内側)的方式(基材% 朝向外側的方式)捲繞於捲芯1上。 若於拉出接著材帶時產生結塊,則於接著劑層的一部 分轉印於基材的背面的情況,有無法於電路構件上的預定 位置配置必需量的接著劑層,連接部的電性連接或機械固 著變得不充分之虞。另外,於接著劑層自基材上剝離而僅 拉出基材的情況,必需使生產設備停止,而使生產性大幅 下降。於電路連接體或半導體晶片、印刷配線板等需要大 量生產的領域等’為了具有成本競爭力,增加單位時間的 生產個數非常重要,即便為數分鐘左右的停止時間,其影 響亦極大。因此,於上述領域中強烈期望改善結塊(專利 文獻2〜專利文獻8)。 專利文獻2、專利文獻3中,記載有自接著材帶的形 狀的觀點考慮來抑制結塊的技術,揭示有於帶側端面,在 4 201139259 比基材的寬度更狹窄的寬度 二接者腦的接讀帶。專利文獻4中,記載有自接著劑 =成,觀財縣抑制結塊的技術,揭料使對基板的 暫時固定力為預定範圍内的接著材帶。專利文獻5中,記 f有自使用條件的觀點考慮來抑制結塊的技術,揭示有具 有控制捲筒溫度的機構的貼附《置。專利文獻6中1載 ==接著材帶的捲筒零件的結構的觀點考慮來抑制 有,設置於側板上的肋狀結構具有導電性 獻7中’記載有自基材的構成的觀 ^考慮來抑騎塊的技術,揭示有使驗表背面的表面 々ίϊϊ勢差的材質作為基材的捲重體。專利文獻8中,、 =:結束標示與接著劑的相容性的觀點考慮來抑制結 [先前技術文獻] [專利文獻] 專利文獻1 .日本專利特開2〇〇3_34468號公報 專利文獻2 :國際公開第〇8/〇53824號 專利文獻3 .國際公ρ㈣G·5”2號 專利文獻4 .日本專利特開咖〗··^號 專利文獻5 .日本專利特開⑽⑽8867號公 專利文獻6 ·日本糊朗2_ _354號公 專利文獻7 :日本專利特開平11-293206號公報 專利文獻8 .日本專利特開2〇〇1_284〇〇5號公 如上述專利文獻2〜專矛丨 k J文獻8所s己载,自電路連接 201139259 但現狀為尚未發現劃時 慮,對結塊的防止對策進行研究, 代的解決對策。 【發明内容】Circuit, LSI) A material for electrically connecting and mechanically fixing a conductor element or a package member in order to maintain a conductive state of the opposing electrodes and to keep the adjacent electrodes insulated from each other. In addition to the anisotropic conductive film, a known material such as a non-conductive film (NCF) is used. The connecting material includes an adhesive component containing a thermosetting resin and conductive particles which are optionally formulated according to the case of the anisotropic conductive film, and is used in a base such as a polyethylene terephthalate film (PET film). The film is formed into a film. The entire material of the obtained film is cut into a strip shape so as to have a width suitable for the application, and is wound around a winding core to produce a backing roll (see Patent Document 1). However, one of the reasons for the decrease in the connection reliability of the circuit connector is the phenomenon of agglomeration in 201139259. The agglomeration refers to a phenomenon in which the adhesive layer is transferred to the back surface of the substrate when the adhesive tape in the wound state is pulled out. The adhesive layer provided on one side of the substrate is in an uncured state, and thus has a certain degree of fluidity. If the backing roll is placed for a long time, there is a case where the adhesive oozes from the end face of the tape, and the adhesive adheres to the side plate of the roll. When the adhesive tape is pulled out from the roll in this state, there is a problem that a part of the adhesive layer is transferred to the back surface of the substrate, or the adhesive layer is peeled off from the substrate to pull out only the substrate. The situation of the bad state. Fig. 9 is a cross-sectional view schematically showing an example of agglomerates generated when a subsequent tape is pulled from a previous material roll. The adhesive tape 25 shown in Fig. 9 is wound around the winding core 1 so that the adhesive layer 28 faces the core side (inner side) (the substrate % faces outward). When agglomeration occurs when the adhesive tape is pulled out, when a part of the adhesive layer is transferred to the back surface of the substrate, a necessary amount of the adhesive layer cannot be disposed at a predetermined position on the circuit member, and the connection portion is electrically charged. Sexual connections or mechanical fixation become inadequate. Further, in the case where the adhesive layer is peeled off from the substrate and only the substrate is pulled out, it is necessary to stop the production equipment, and the productivity is drastically lowered. In the field of circuit connectors, semiconductor wafers, and printed wiring boards, which require a large amount of production, etc., in order to be cost-competitive, it is very important to increase the number of production per unit time, and even if the stop time is several minutes or so, the influence is extremely large. Therefore, it has been strongly desired to improve agglomeration in the above-mentioned fields (Patent Document 2 to Patent Document 8). Patent Document 2 and Patent Document 3 describe a technique for suppressing agglomeration from the viewpoint of the shape of the adhesive tape, and discloses a width of the two-bit brain which is narrower than the width of the substrate at 4 201139259. Reading tape. Patent Document 4 describes a technique for suppressing agglomeration by the self-adhesive agent = Cheng, and the release material has a temporary fixing force to the substrate within a predetermined range. In Patent Document 5, it is noted that f has a technique for suppressing agglomeration from the viewpoint of use conditions, and discloses a device having a mechanism for controlling the temperature of the reel. In the case of the structure of the roll member of the material tape, the rib structure provided on the side plate is electrically conductive, and the structure of the base material is described. The technique of suppressing the riding block reveals a weight body having a surface 々ίϊϊ potential difference on the back surface of the inspection table as a base material. In the case of the patent document 8, the following is a viewpoint of the end point of the mark and the compatibility of the adhesive agent. [Prior Art Document] [Patent Document] Patent Document 1. Japanese Patent Laid-Open Publication No. Hei 2 No. Hei. Japanese Laid-Open Patent Publication No. Hei. No. Hei. No. Hei. No. Hei. No. Hei. No. Hei. No. Hei. No. Hei. Japanese Laid-Open Patent Publication No. Hei. No. Hei. No. Hei. No. Hei. No. Hei. No. Hei. No. Hei. No. Hei. No. Hei. No. Hei. s self-contained, self-circuit connection 201139259 However, the current situation is that no consideration has been found, and the prevention measures against agglomeration are studied, and the countermeasures are replaced. [Summary of the Invention]

層自基材上剝離而僅拉出基材的不良狀態。 n/、 從伐耆材捲筒,其於 可以極高的水準抑制接著劑 的不良狀態。以下,本說明 ^中所謂「結塊」,是表示「於拉出捲繞狀態的接著材帶時, 接著劑層自基材上剝離而僅拉出基材的不良狀態」。 本發明的接著材捲筒包括:捲芯;一對側板,其以相 互對向的方式設置於捲芯的兩侧;以及接著材帶,其具有 帶狀基材及設置於該基材的—面上的接著㈣,且ς繞於 捲芯上;並且上述接著材較以基材的未形成接著劑層的 面朝向捲芯側的方式捲繞於捲芯上。 先别,於接著材捲筒的領域中常識為,為了保蠖接 劑層遠離外部環境,而以接著劑層朝向捲芯側(⑴則),並 且基材朝向外側的方式將接著材帶捲繞於捲芯上(參照上 述專利文獻2的圖3、圖4)。例如,若使接著劑層朝向外 側,則存在接著騎上附著塵埃等不良狀態。尤其是用於 電子材料的接著材帶即便是少量的塵埃亦會導致製σ 良’因此藉由使接著朝向捲⑽彳(關)來捲:以保 護其遠離污染源。 +但是,本發明者等人違反先前的常識,以基材朝向捲 芯側(關)且接著劑層朝向外側的方式將接著材帶捲繞 201139259 於捲芯上而嘗試製作接著材顯。評價該接著材捲筒上有 無產生結塊,結果發現可以極高的水準防止結塊。 可藉由使接著材帶的表背面與先前相反來高度抑制結 塊的原因未必明確,但本發明者等人推測如下。即認為, 本發明中,即便接著劑自接著材帶的接著劑層的端面渗出 而黏接著於侧板上,亦於拉出該帶時,由於位於比接著劑 層更靠捲糊(關)絲概起接,故而在所拉 出的接著材帶的接著_與所拉出的接著 欲剝離的力未發揮_,且來自黏接著於側板的部分的景; 響小’因此可達成結塊的抑制。 先刖,由於容易產生結塊,故而對可捲繞於捲芯上的 接著材帶的長度存在關,但藉由採訂述構成,可與先 前品相比使接著材帶更長條化(例如2〇〇 m以上)。 除接著材帶的長條化以外,依據本發明,可將黏度比 較低而於先前技術巾容易產生結塊的接著顧於接著劑 層。本發财,接著騎較佳為於3(rc的剪切黏度為 10=00 Pa.s以下。低黏度的接著劑例如為熱自由基硬化型 接著劑’可列舉低溫硬化^接著劑。低溫硬化型接著劑要 求提高低溫⑷如丨观〜丨赃)下的流雜。具體例可 列舉含有1分鐘半衰期溫度為16忙以下的自由基聚合起 始劑的熱自由基硬化型接著劑。 依據本發明,即便接著劑層含有大量於3CTC為液狀的 材料而流動性比較高,亦可充分抑制結塊。於上述熱自由 基硬化型接賴含有熱龍樹脂、包含於贼為液狀的自 201139259 由基聚合性物質的自由基聚合性材料、及自由基聚合起始 劑的情況,先前的接著材捲筒中容易以高機率產生結塊。 相對於此,本發明的接著材捲筒中,即便相對於熱塑性樹 脂及自由基聚合性材料的總量100質量份,熱自由基硬化 型接著劑中的上述自由基聚合性物質的含量為2〇質量份 〜80質量份’亦可充分抑制結塊。 枨耆劑層1马含有熱塑性樹脂、包含於3(rc為液狀白 環氧樹脂的熱硬化性材料、及硬化劑的環氧系接著劑。在 時’先前的接著材捲筒中’料以高解產生結塊,但^ 發明的接著材捲筒巾,即便相躲熱塑雜脂及熱硬化,卜 材料的總量1GG質量份’環氧系接著射的環細 的含量為2G質量份,質量份,亦可充分抑制結^樹 ㈣’接者劑層的無機填料含量以該接著劑層& 體積為基準時可為2〇體積百分比(vg1%)以下。藉由4 中調配無機填料,可使接著劑層的流動性降低布 填料。本發明,即便不在接著劑層中調配無相 Ϊ科,或者即便無機填料的調配量為20體積%以下,亦^ 充分抑制結塊。 質量=可;=的百無機 ::便不在_中調 1 配‘;= 上述二氧切的含二 旱時,較佳為35質量%以下。於使用氧 8 201139259 化鋁作為無機填料的情況,上述氧化鋁的含量以上述 劑層的質量為基準時,較佳為5〇質量%以下。 接體 依據本發明,即便接著材帶的寬度為〇5 mm〜3〇 mm ’亦可充分抑制結塊。寬度狹窄的帶與寬度粗的帶相 比較,帶端面的接著劑滲出的影響相對較大,容易產生结 塊二上述接著材帶適宜用於電路連接。如上所述,由於; 以南水準抑制結塊,故而可製造連接可靠性優異的電路連 [發明的效果] 依據本發明,當拉出捲繞狀態的接著材帶時,可以極 高的水準抑制接著劑層自基材上剝離。 ^為讓本發明之上述和其他目的、特徵和優點能更明顯 易懂,下文特舉較佳實施例,並配合所附圖式,作詳細說 明如下。 、° 【實施方式】 以下,一邊參照隨附圖式,一邊對本發明的較佳實施 形態進行詳細說明。此外,圖式的說明中對同一要素標註 同一符號’省略重複的說明❶另外,為了圖式的便利,圖 式的尺寸比率與所說明的比率未必一致。 圖1所示的接著材捲筒10包括筒狀的捲芯1、及以相 互對向的方式配置於捲芯1的轴方向的兩侧的一對側板 2。如圖2所示,於捲芯1的外表面F1上捲繞異向導電帶 (接著材帶)5,構成捲重體。異向導電帶5是以基材6 的未形成接著劑層的面朝向捲芯1側且接著劑層8朝向外 201139259 ::2捲=芯1上。於捲重體的狀態下,基材6的 ㈣者綱#面與—捲内側的異向導電帶5的接著 劑層8直接接觸。 藉由以如上所述的朝向將異向導電帶5捲繞於捲芯^ 層8 =電帶5時,以極高的水準抑制接著劑 X自基材6上剝離而僅拉出基材的不良狀態。此外,側 板較佳為⑤置於捲芯的轴方向的兩端部,其原因在於將多 個接著材捲筒制—聽管,但村崎糾一部分穿 透側板而自側板的外側面突出的方式設置側板。 如圖3所示,侧板2在與異向導電帶5鄰接的内側面 F2上具備自φ F2上隆敎自貫軌%㈣緣起放射狀地 延伸存在的肋狀結構部2b。藉由設置肋狀結構部2b,即便 接著劑自異向導f帶5的端面滲$,亦可充分縮小接著劑 黏接著於側板2上的面積,因此可與本發明配合而有效地 抑制結塊。 此外,如圖1、圖2所示,接著材捲筒1〇具有壓接裝 置(未圖示)的旋轉軸所插入的軸孔l〇a,且該軸孔l〇a 上設置有與設置於旋轉軸上的凸部嵌合的缺口部1〇b。其 中’若為當將接著材捲筒10安裝於壓接裝置的旋轉軸上時 可防止空轉的構成,則亦可採用缺口部10b以外的構成。 具備捲芯1及侧板2的捲筒零件可使用塑膠成型品等。 如圖4所示’異向導電帶5具備帶狀基材6、及形成 於基材6的一面上的接著劑層8。 異向導電帶5的長度較佳為1 m〜1〇〇〇 m,更佳為200 201139259 m〜1000 m,尤佳為200 m〜500 m,進而更佳為250 m〜 500 m,特佳為300 m〜500 m。先前,由於容易產生結塊, 故而可捲繞於捲芯1上的異向導電帶5的長度存在限制, 但藉由以基材6朝向内侧的方式將異向導電帶5捲繞於捲 芯1上’可將比先前品更長的異向導電帶5捲繞於捲芯1 上。 異向導電帶5的寬度較佳為0.5 mm〜30 mm,更佳為 0.5 mm〜3.0 mm,尤佳為 0.5 mm〜2.0 mm,特佳為 〇.5mm 〜1.0 mm。先前,由於容易產生結塊,故而可捲繞於捲芯 1上的異向導電帶5的寬度存在限制,但藉由以基材6朝 向内側的方式將異向導電帶5捲繞於捲芯1上,可將寬度 比先前品狹窄的異向導電帶5捲繞於捲芯1上。此外,基 材6的寬度較佳為與形成於該基材6上的接著劑層8的寬 度相同,或者比接著劑層8的寬度更寬。接著劑層8的寬 度只要根據使用用途來調整即可。 接著劑層8的厚度只要根據所使用的接著劑成分及被 接著物的種類等來適當選擇即可’較佳為5 μηι〜1〇〇 μιη, 更佳為10 μιη〜40 μιη。先前,由於容易產生結塊,故而可 捲繞於捲芯1上的異向導電帶5的接著劑層8的厚度存在 限制,但藉由以基材6朝向内侧的方式將異向導電帶5捲 繞於捲芯1上,亦可捲繞包括比具有例如3〇 μιη〜1〇〇 pm 左右厚度的先前品更厚的接著劑層8的異向導電帶5。此 外,基材ό的厚度較佳為4 μιη〜200 左右,更佳為2〇 μιη 〜100 μιη 〇 π 201139259 基材6例如可使用包含聚對苯二曱酸乙二酯、聚萘二 曱酸乙二酯(polyethylene naphthalate )、聚間苯二甲酸乙 二醋(polyethylene isophthalate )、聚對苯二甲酸丁二醋 (polybutylene terephthalate)、聚烯烴(polyolefin)、聚乙 酸酯(polyacetate)、聚碳酸酯(polycarbonate)、聚苯硫峻 (polyphenylene sulfide)、聚酿胺(polyamide)、乙烯-乙 酸乙烯酯共聚物、聚氯乙烯(polyvinyl chloride)、聚偏二 氯乙烯(polyvinylidene chloride)、合成橡膠系、液晶聚合 物等的各種塑膠帶。但是,構成基材6的材質並不限定於 該些材質。另外,基材6亦可使用對與接著劑層8的抵接 面等實施了脫模處理的基材。進而,可為選自上述材料中 的2種以上混合而成的基材,或者將上述膜多層化而成的 基材。 接著劑層8的接著劑成分8a可廣泛應用藉由熱或光而 表現出硬化性的材料,可使用環氧系接著劑或者自由基項 化型接著•或者可使用聚胺基?酸§旨(pQlyurethane)或 聚乙稀基S旨(pGlyvinyleste〇等熱塑性接著劑。由於連接 後的耐熱性或耐祕優異,故而錄為使用交聯性材料。 S ’含有作域硬化性樹脂的環氧細旨作為主成分的環 ,二著劑就可短時間硬化料接作業性良好,分子結榻 劑且特徵而言較佳。另外,自由基硬化型接著 :著劑更低溫短時間的硬化性優異等特 徵,可根據用途來適當選擇。 衣氧系接著軸如含有環氧_旨等熱硬化性材料及項 12 201139259 化劑而成°另外,通常視需要而調配熱塑性樹脂、偶合劑、 填充劑等》 上述環氧樹脂例如可列舉:雙紛A (bisphen〇i a)型 環氧樹脂、雙紛F (bisphen〇1 F)型環氧樹脂、雙驗s (Μ—8)型環氧樹脂、苯紛_ (phen0ln0V0lac) ^•環氧細Θ、甲騎酸(_Q1 nQVGlae)型環氧樹脂、雙 龄A祕(bisphen〇1 An〇v〇lac)型環氧樹脂、伽F _ iTr\Fnovolac) ^ 水甘油酉曰(glycidyl ester)型環氧樹脂、縮水甘油 rm氧樹脂、乙内酶(h細0in)型環氧樹脂、 t (lS;cyanurate> 、a。k些環氧樹脂可經_化,亦可經氫化。另外, ==酿基或甲基丙稀酿基加成於環氧樹脂的側鏈。 〜衣氧樹脂可單獨使用W,或者將2種以上組合使用。 轉3ΓΓ要是可使環氧樹脂硬化的硬化劑,則並 陽硬化劑、 =離子聚合性__硬倾、聚加成型的硬 中,就速硬化性優異、不需要化學當量的考慮的〆 ^面而吕’較佳為陰離子或者陽離子聚合性的觸媒型硬化 列舉上子或者陽離子聚合性的觸媒型硬化劑例如可 歹广•坐(lmldazoIe)系、醯肼(hyd ::、胺錯鹽(。― 、重氮鹽(diazomum salt)、脂肪族疏鹽等)、 13 201139259 胺醯亞胺(amine imide)、二胺基順丁烯二腈(diamin〇 maleonitrile)、三聚氰胺(melamine)及其衍生物、聚胺 (polyamine)的鹽、二氰二胺(dicyandiamide)等,亦可 使用該些化合物的改質物等。上述聚加成型的硬化劑例如 可列舉.聚胺類、聚硫醇(p〇lymercaptan )、聚紛 (polyphenol)、酸酐等。 將該些環氧樹脂的硬化劑以聚胺基曱酸酯系、聚酉旨 (polyester)系等的高分子物質,鎳、銅等的金屬薄膜, 石夕酸舞等的無機物等包覆而微膠囊化的潛在性硬化劑,由 於可使用時間可延長,故而較佳。上述硬化劑可單獨使用 1種,或者將2種以上組合使用。 上述硬化劑的調配量通常相對於熱硬化性材料與視需 要調配的熱塑性樹脂的總量1〇〇質量份,為〇 〇5質量份〜 20質量份左右。 自由基硬化型接著劑例如是含有自由基聚合性材料及 自由基聚合S始劑而成。另外,通常視需要*調配熱塑性 樹脂、偶合劑、填充劑等。 上述自由基聚合性材料只要是例如具有藉由自由基而 聚合的官能基的物質’則可無制限制地使用。具體而言, 例如可列舉:丙稀酸醋(亦包括對應的甲基丙婦酸醋,以 下相同)化合物、丙烯醯氡基(亦包括對應的甲基丙稀酿 氧基以下相同)化合物、順丁稀二酿亞胺(脱麻W) 4 :物甲基順丁婦一醯亞胺(c办沉⑽如此)樹脂、納 迪克醯亞胺(nadimide)樹脂等自由基聚合性物質。該些 201139259 自由基聚合性物質可以單體或者募聚物的狀態使用,亦可 將單體與募聚物併用。 上述丙烯酸酯化合物例如可列舉:丙烯酸曱酯(methyl acrylate )、丙烯酸乙酯(ethyl acrylate )、丙烯酸異丙酯 (isopropyl acrylate )、丙烯酸異丁酯(isobutyl acrylate )、 乙二醇二丙稀酸酯(ethyleneglycol diacrylate)、二乙二醇 二丙稀酸酯(diethyleneglycol diacrylate )、三經曱基丙烧 三丙稀酸醋(trimethylolpropane triacrylate )、四經曱基曱 烧四丙稀酸醋(tetramethylolmethane tetraacrylate)、2-經基 -1,3- 二 丙 烯 醯 氧 基 丙 烷 (2-hydroxy-1,3-diacryloxypropane )、2,2-雙[4-(丙烯醯氧基 甲氧基)苯基]丙烷 (2,2-bis[4-(acryloxymethoxy)phenyl]propane )、2,2-雙 [4-(丙烯醯氧基多乙氧基)苯基]丙烷(2,2_bis[4-(acryl〇xy polyethoxy)phenyl]propane )、丙烯酸二環戊烯醋 (dicyclopentenyl acrylate )、丙稀酸三環癸酯 (tricyclodecanyl acrylate)、異三聚氰酸三(丙烯醯氧基乙 基)酯(tris(acryloyloxyethyl)isocyanurate)、丙稀酸胺基甲 酸酯(urertianeacrylate)等。另外,可視需要而適當使用 對苯二酚(hydroquinone )、甲醚對苯二酚(methyiettler hydroquinone )類等的聚合抑制劑。另外,就耐熱性提高 的觀點而言,較佳為丙烯酸酯化合物等自由基聚合性物質 具有至少1種二環戊烯基、三環癸基、三嗪環等取代基。 上述丙稀酸酯化合物以外的自由基聚合性物質例如可 15 201139259 適宜使用國際公開第2009/063827號所記載的化合物。該 些化合物可單獨使用1種,或者將2種以上組合使用。 上述自由基聚合起始劑只要是例如藉由加熱或光的照 射而分解產生游離自由基的化合物,則可無特別限制地使 用。具體而言’例如可列舉過氧化化合物、偶氮系化合物 等。此種硬化劑可根據作為目標的連接溫度、連接時間、 使用期限等來適當選定。 自由基聚合起始劑更具體而言可列舉:二醯基過氧化 物 (diacyl peroxide )、 過氧化二碳酸酯 (peroxydicarbonate )、過氧醋(per0Xyest;er )、過氧縮 _ (peroxyketal)、二烷基過氧化物(dialkylper〇xide)、氫過 氧化物(hydroperoxide)、甲矽烷基過氧化物(Siiyi peroxide) 等。該些自由基聚合起始劑中,較佳為過氧酯、二烷基過 氧化物、氫過氧化物、矽烷基過氧化物等,更佳為獲得高 反應性的過氧酯。該些自由基聚合起始劑例如可適宜使用 國際公開第2009/063827號所記載的化合物。該些自由基 聚合起始劑可單獨使用1種,或者將2種以上組合使用。 上述自由基聚合起始劑的調配量通常相對於自由基聚 合性材料與視需要而調配的熱塑性樹脂的總量100質量 份,為0.1質量份〜1〇質量份左右。 該些環氧系接著劑以及自由基硬化型接著劑中視需要 而調配的熱塑性樹脂例如為容易對接著劑賦予膜性的樹 月曰該些熱塑性樹脂例如可列舉:苯氧基(phen〇Xy)樹脂、 聚乙烯醇縮甲醛(Polyvinyl formal )樹脂、聚苯乙烯 16 201139259. (polystyrene)樹脂、聚乙烯醇縮丁醛(p〇iyVinyi butyral) 樹脂、聚酯樹脂、聚醯胺樹脂、二甲苯樹脂、聚胺基曱酸 酉旨樹脂、聚醋胺基曱酸醋樹脂、酴樹脂、萜豨岭(terpene phenol)樹脂等。該些熱塑性樹脂例如可適宜使用國際公 開第2009/063827號所記載的化合物。該些化合物中,就 接著性、相容性、耐熱性、機械強度等優異的方面而言, 較佳為苯氧基樹脂。該些樹脂可單獨使用1種,或者將2 種以上組合使用。 於調配於環氧系接著劑中的情況,相對於熱塑性樹脂 及熱硬化性材料的總量1〇〇質量份,該熱塑性樹脂的調配 量通常為5質量份〜80質量份左右。另外,於自由基硬化 型接著劑中調配熱塑性樹脂的情況,熱塑性樹脂的調配量 相對於熱塑性樹脂及自由基聚合性材料的總量質量 伤’通常為5質量份〜80質量份左右。 藉由以基材6朝向内侧的方式將異向導電帶5捲繞於 捲心1上,可將黏度比較低且於先前的技術中容易產生結 塊的接著劑用於接著劑層中。接著劑層8若於3〇<t的剪切 黏度為100000 Pa.s以下即可。該黏度更佳為1〇〇〇 Pa s〜 50000 Pa_s,尤佳為1000 Pa.s〜3〇〇〇〇卩以。低黏度的接著 劑成分8a為熱自由基硬化型接著劑,可列舉低溫硬化型的 接著劑。其具體例可列舉含有丨分鐘半衰期溫度為16(rc 以下的自由基聚合起始劑的熱自由基硬化型接著劑。i分 鐘半衰期溫度更佳為机〜丨贼,尤佳為_〜l2〇(>c。 此種硬化劑可列舉:二·第三丁基過氧化六氣對苯二甲酸酿 17 201139259 (1分鐘半衰期溫度:142°C,Kayaku Akzo股份有限公司 公司製造的HTP-65W(商品名))、經取代的笨曱酿基過氧 化物(1分鐘半衰期溫度:13U〇C,日本油脂股份^限公 司製造,Nyper BMT (商品名))、二月桂醯基過氧化物(】 分鐘半农期溫度:116.4°C ’日本油脂股份有限公司製造, PeroylL (商品名))等。 低點度的接著劑成分8a的其他例子可列舉含有熱塑 性樹脂、包含30。〇為液狀的自由基聚合性物質的自由^聚 合性材料、及自由基聚合起始劑的熱自由基硬化型接著 劑。熱自由基硬化型接著劑中的上述自由基聚合性物質的 含量相對於熱塑性樹脂及自由基聚合性材料的總量1〇〇質 量份,較佳為20質量份〜80質量份。該含量更佳為3〇質 量份〜80質量份’尤佳為4〇質量份〜8〇質量份。 接著劑成分8a可為含有熱塑性樹脂、包含為液 狀的環氧樹脂的熱硬化性材料、及硬化劑而成的環氧系接 者劑。此時,環氧系接著劑中的上述環氧樹脂的含量相對 於熱塑性樹脂及熱硬化性材料的總量1〇〇質量份,較佳為 2〇質量份〜8〇質量份。該含量更佳為4〇質量份〜8〇質量 份,尤佳為30質量份〜80質量份。 此外’於將1C晶片安裝於玻璃基板或可撓性印刷基板 (FPC)上的情況,自抑制由晶片與基板的線膨服係數 的差所產生的基板翹曲的觀點考慮,較佳為將發揮内部應 力的緩和作用的成分調配於接著劑成分中。具體而言,較 佳為於接著材成分中調配丙烯酸系橡膠或彈性體成分。另 18 i. i.201139259 ^型^::丨用如國際公開第98/44067號所記载的自由基硬 金屬例如可列舉Au、Ag、Ni、Cu、焊料等的 鄉mi寻。另外,亦可為以非導電性的玻璃、陶瓷、 物·^I核’於該核上包覆上述金屬或碳的膜、或者金屬 或熱溶融若導電粒子8b為以塑膠為核的導電粒子 可於連接子’於加熱加壓時具有變形性。因此’ 接可靠性時0大電極與導電粒子8b的接觸面積,可提高連 可添加將導電粒子8b的表面進而以高分子樹 “二⑽緣性粒子。藉由添加絕緣性粒子,於增加粒 子彼絲量的情況’ #用作異向導電帶時可抑制由粒 所引起的短路,可提高鄰接的電路電極間的 此外,可將選自絕緣性粒子及導電粒子中的!種 導或者將2種粒子組合使用。就使分散性及 良好的她,導電粒子及絕緣性粒子的平均粒 從較佳為1 μΠ1〜18帅,更佳為2.5 μπι〜10 μιη。 子8b的調配量並無特別限制’以接著劑成分整 2基準時,較佳為W體積%〜3G體義,更佳為(Π /〇〜10體積%,尤佳為〇 5體積%〜5體積%。若導電 $子8b的調配量小於〇]體積%,則存在優異的導電性受 ,的傾向’若超過3。體積%,畴在相作肠導電帶時 谷易產生電路的短路的傾向。 為了使接著劑層8的流動性下降,有時將無機填料調 201139259 配於接著劑成分8 a中。無機填料只要是例如固體粒子狀的 無機化合物’則並無特別限定。無機填料的材質的具體例, 例如可列舉:氫氧化IS、氫氧化鎂、碳酸辦、碳酸鎮、石夕 酸辦、石夕酸鎮、氧化詞、氧化鎮、氧化铭、氮化铭、、職 鋁晶鬚(aluminum borate whisker)、氮化硼、結晶性二氧 化石夕或非晶性二氧化料二氧切、銻氧化物等。益 料可單獨使用1種,或者將2種以上組合使用。… 本實施形態中,藉由以基材6朝向捲芯側(内側)的 方式將異向導電帶5純於捲芯丨±,即财在接著劑層 8中調配無_料’或者即便以接著_ 8的體積為基準 1將調配量設為20體積%以下,亦可充分抑制結塊。無機 填料含量更佳為0體積%〜15體積%,尤佳為Q體積%〜 1〇體積%。 另外,即便將以接著劑層8的f量4 t量料5G質量灿下,亦可充分抑制結塊。無機= 3量更佳為G質量%〜4G f量%,尤佳為G質量%〜3〇質 ,%。無機填料的比重根據義而有所不同,故而質量基 =的含量較佳為根據所使用的無機填料而狀為適當的 層:料為二氧化矽的情況’即便將以接著劑 ^的質#為基準時的含4設為% f量%以下,亦可充分 P^J結塊。二氧化石夕含量更佳為〇質量%〜3〇質量%,尤 即二I2 2G質量%。於無機填料為氧化18的情況’ 以接著綱8的質量為基準時的含量設為5〇質量% 乂下’亦可充分抑制結I氧她含量更佳為G質量%〜 20 201139259 & 40質量%,尤佳為〇質量%〜3〇質量%。 接著可料地計算’但於自 定。 丁叙的情況,例如可利用以下方法測 的電爐(於空氣環先升溫至靴的溫度 見^甲加熱45分鐘。 測填料的含量的 密電子天平,製作所製造的精 ru^、τ,)測小數點後3位(0.0〇U)。 入接菩㈣% Γ上玫置撕’於贿翻自接著材帶上放 入接者劑層約1 g。料’ _量是於23机姻〇蠢、 1個大氣壓下進行。 (4) 將加入有接著劑層的坩堝與(1)同樣地在電爐 中加熱45分鐘。藉由該加熱,接著_成為灰分。 (5) 將電爐的溫度恢復至常溫,於乾燥器中迅速地以 與上述(2)、(3)相同的方法稱量自電爐中取出的坩堝及 灰分的質量。 (6) 自(5)中獲得的坩堝及灰分的質量中減去(2) 中獲得的掛堝的質量,算出灰分的質量。該灰分中應當包 含無機填料及導電粒子(金屬成分)。 (7) 灰分中所含的導電粒子(金屬成分)的種類及含 量是利用感應輕合電漿(Inductively Coupled Plasma,ICP) 發光分光分析法來分別算出。此時,將灰分以氩氟酸及硝 21 201139259 酸的混酸分解而製成供 置The layer is peeled off from the substrate to pull out the poor state of the substrate. n/, from the cutting of the coffin, which can suppress the bad state of the adhesive at a very high level. In the following description, "caking" refers to "a defective state in which the underlayer is peeled off from the substrate and the substrate is pulled out only when the adhesive tape is pulled out." The binder roll of the present invention comprises: a core; a pair of side plates disposed on opposite sides of the core in a mutually opposing manner; and a subsequent strip having a strip substrate and disposed on the substrate - The surface is followed by (4) and wound on the core; and the above-mentioned bonding material is wound on the winding core so that the surface of the substrate on which the adhesive layer is not formed faces the winding core side. In the field of the material roll, it is common knowledge that in order to keep the sizing agent layer away from the external environment, the adhesive layer is rolled toward the core side ((1)), and the substrate is oriented toward the outside. It is wound around a core (refer to FIG. 3 and FIG. 4 of the above-mentioned patent document 2). For example, when the adhesive layer is directed to the outside, there is a problem that a dust or the like adheres to the dust. In particular, even a small amount of dust used in the adhesive tape of the electronic material causes the σ to be made, so that it is subsequently wound toward the roll (10) to protect it from the source of contamination. However, the inventors of the present invention have attempted to fabricate a subsequent material in a manner that the substrate tape is wound toward the core side (closed) and the adhesive layer is directed outward, so that the adhesive tape is wound on the core, in violation of the conventional knowledge. The presence or absence of agglomeration on the web of the laminate was evaluated, and it was found that the agglomeration was prevented at an extremely high level. The reason why the agglomeration of the back surface of the adhesive tape can be highly suppressed by the reverse of the front surface is not necessarily clear, but the inventors of the present invention presume the following. That is, in the present invention, even if the adhesive is adhered to the side plate from the end surface of the adhesive layer of the adhesive tape, the tape is pulled out more than the adhesive layer when the tape is pulled out. The wire is spliced, so that the force of the subsequent strip to be pulled out and the force to be peeled off is not exerted, and the view from the portion adhered to the side panel is small; Block suppression. First, since the agglomeration is easy to occur, the length of the adhesive tape that can be wound around the winding core is closed, but by the configuration, the adhesive tape can be made longer than the prior art ( For example, 2〇〇m or more). In addition to the subsequent striping of the strip, in accordance with the present invention, the viscosity ratio can be lowered and the prior art towel is susceptible to agglomeration followed by the adhesive layer. This is a fortune, and then the ride is preferably 3 (the shear viscosity of rc is 10=00 Pa.s or less. The low-viscosity adhesive is, for example, a thermal radical-curable adhesive), which can be cited as a low-temperature hardening adhesive. The hardening type of adhesive is required to increase the flow under low temperature (4) such as 丨 丨赃 ~ 丨赃. Specific examples thereof include a thermal radical curing type adhesive containing a radical polymerization initiator having a one-minute half-life temperature of 16 or less. According to the present invention, even if the adhesive layer contains a large amount of a material in which 3CTC is liquid, the fluidity is relatively high, and agglomeration can be sufficiently suppressed. In the case where the above-mentioned thermal radical curing type is provided with a heat-radical resin, a radical polymerizable material derived from a base polymerizable substance from 201139259, and a radical polymerization initiator in a liquid form, the previous laminate roll is used. It is easy to produce agglomeration in a high probability in the cylinder. On the other hand, in the binder roll of the present invention, the content of the radical polymerizable substance in the thermal radical-curable adhesive is 2 即便 with respect to 100 parts by mass of the total amount of the thermoplastic resin and the radical polymerizable material. The mass parts of -80 parts by mass' can also sufficiently inhibit the agglomeration. The elixir layer 1 contains a thermoplastic resin, an epoxy-based adhesive contained in 3 (rc is a thermosetting material of liquid white epoxy resin, and a curing agent.) In the 'previous backing roll' The high solution produces agglomerates, but the invented web roll of the invention, even if it is separated from the thermoplastic resin and the heat hardening, the total amount of the material of the material is 1 GG parts by mass, and the content of the ring of the epoxy-based film is 2 G parts by mass. , the mass part, can also fully suppress the inorganic filler content of the connector layer (4) 'the carrier layer can be 2 〇 volume percentage (vg1%) or less based on the volume of the adhesive layer & volume. The filler can reduce the fluidity of the adhesive layer to reduce the agglomerate. In the present invention, even if the non-phase is not disposed in the adhesive layer, or even if the amount of the inorganic filler is 20% by volume or less, the agglomeration is sufficiently suppressed. Yes; = hundred inorganic:: it is not in the middle of the 1 with '; = = above the dioxane containing the second drought, preferably less than 35 mass%. In the case of using oxygen 8 201139259 aluminum as an inorganic filler, the above When the content of alumina is based on the mass of the above-mentioned agent layer, Preferably, it is 5 〇 mass% or less. According to the present invention, agglomeration can be sufficiently suppressed even if the width of the subsequent material tape is 〇5 mm to 3 〇mm'. The narrow width band is compared with the thick width band. The influence of the adhesive bleed out is relatively large, and it is easy to produce agglomerate. The above-mentioned adhesive tape is suitable for circuit connection. As described above, since the agglomeration is suppressed at a south level, it is possible to manufacture a circuit having excellent connection reliability. EFFECTS According to the present invention, the peeling of the adhesive layer from the substrate can be suppressed at an extremely high level when the adhesive tape in the wound state is pulled out. ^ To make the above and other objects, features and advantages of the present invention more DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS Hereinafter, preferred embodiments of the present invention will be described in detail with reference to the accompanying drawings. In the description of the drawings, the same elements are denoted by the same reference numerals, and the description thereof will not be repeated. In addition, for the convenience of the drawings, the size ratio of the drawings does not necessarily coincide with the illustrated ratio. The backing material roll 10 shown in Fig. 1 includes a cylindrical core 1 and a pair of side plates 2 which are disposed on opposite sides of the winding core 1 in the axial direction so as to face each other. An opposite conductive tape (subsequent material tape) 5 is wound around the outer surface F1 of the core 1 to constitute a roll weight. The isotropic conductive tape 5 is directed toward the core 1 side of the surface of the substrate 6 where the adhesive layer is not formed, and then The agent layer 8 faces outwards 201139259: 2 rolls = core 1. In the state of the roll weight, the (four) face of the substrate 6 is in direct contact with the adhesive layer 8 of the anisotropic conductive tape 5 on the inside of the roll. When the isotropic conductive tape 5 is wound around the core layer 8 = the electric tape 5 in the orientation as described above, the adhesion of the adhesive X from the substrate 6 is suppressed at an extremely high level, and only the substrate is pulled out. In addition, the side plates are preferably placed at both ends of the winding core in the axial direction, because the plurality of the backing materials are wound into the tube, but the part of the Tsukisaki penetrates the side plate from the outer side of the side plate. The side panels are set in a prominent way. As shown in Fig. 3, the side plate 2 is provided with a rib-like structural portion 2b extending radially from the edge of the φ F2 on the inner side surface F2 adjacent to the anisotropic conductive strip 5 so as to extend radially from the edge of the ridge F4. By providing the rib-like structure portion 2b, even if the adhesive agent permeates from the end face of the different-direction f-belt 5, the area of the adhesive adhered to the side plate 2 can be sufficiently reduced, so that the agglomeration can be effectively suppressed in accordance with the present invention. . Further, as shown in FIG. 1 and FIG. 2, the material roll 1〇 has a shaft hole l〇a into which a rotating shaft of a crimping device (not shown) is inserted, and the shaft hole l〇a is provided with and set. A notch portion 1bb fitted to the convex portion on the rotating shaft. Here, the configuration other than the notch portion 10b may be employed if the configuration in which the secondary reel 10 is attached to the rotating shaft of the crimping device while preventing the idling. A plastic molded article or the like can be used for the reel parts including the winding core 1 and the side plate 2. As shown in Fig. 4, the anisotropic conductive tape 5 is provided with a belt-like base material 6 and an adhesive layer 8 formed on one surface of the base material 6. The length of the anisotropic conductive strip 5 is preferably 1 m to 1 μm, more preferably 200 201139259 m to 1000 m, particularly preferably 200 m to 500 m, and even more preferably 250 m to 500 m, which is particularly good. It is 300 m to 500 m. Previously, since the agglomeration was liable to occur, the length of the anisotropic conductive tape 5 which can be wound around the core 1 was limited, but the anisotropic conductive tape 5 was wound around the core by the substrate 6 facing inward. 1 upper 'can wind the opposite conductive strip 5 longer than the previous product on the winding core 1. The width of the anisotropic conductive tape 5 is preferably from 0.5 mm to 30 mm, more preferably from 0.5 mm to 3.0 mm, even more preferably from 0.5 mm to 2.0 mm, and particularly preferably from 〇.5 mm to 1.0 mm. Previously, since the agglomeration was liable to occur, the width of the anisotropic conductive tape 5 which can be wound around the winding core 1 was limited, but the anisotropic conductive tape 5 was wound around the core by the substrate 6 facing inward. On the 1st, the anisotropic conductive tape 5 having a narrower width than the previous product can be wound around the winding core 1. Further, the width of the substrate 6 is preferably the same as the width of the adhesive layer 8 formed on the substrate 6, or wider than the width of the adhesive layer 8. The width of the subsequent agent layer 8 may be adjusted according to the intended use. The thickness of the adhesive layer 8 may be appropriately selected depending on the adhesive component to be used and the type of the material to be used, etc., preferably 5 μηι to 1 μm, more preferably 10 μm to 40 μm. Previously, since the agglomeration is liable to occur, the thickness of the adhesive layer 8 of the anisotropic conductive tape 5 which can be wound around the winding core 1 is limited, but the anisotropic conductive tape 5 is formed in such a manner that the substrate 6 faces inward. Winding on the core 1, it is also possible to wind up the anisotropic conductive tape 5 including the adhesive layer 8 which is thicker than the previous product having a thickness of, for example, about 3 μm to 1 μm. In addition, the thickness of the substrate ό is preferably about 4 μm to about 200, more preferably 2 〇μιη to 100 μπη 〇π 201139259. The substrate 6 can be, for example, polyethylene terephthalate or polynaphthalene. Polyethylene naphthalate, polyethylene isophthalate, polybutylene terephthalate, polyolefin, polyacetate, polycarbonate Polycarbonate, polyphenylene sulfide, polyamide, ethylene-vinyl acetate copolymer, polyvinyl chloride, polyvinylidene chloride, synthetic rubber Various plastic tapes such as liquid crystal polymers. However, the material constituting the substrate 6 is not limited to these materials. Further, as the substrate 6, a substrate subjected to mold release treatment such as a contact surface with the adhesive layer 8 may be used. Further, it may be a substrate obtained by mixing two or more kinds selected from the above materials, or a substrate obtained by multilayering the above film. The adhesive component 8a of the adhesive layer 8 can be widely applied to a material which exhibits curability by heat or light, and an epoxy-based adhesive or a radical-reactive type can be used. Alternatively, or a polyamine group can be used. Acetic acid (pQlyurethane) or polyethylene based S (a thermoplastic adhesive such as pGlyvinyleste®. It is considered to be a crosslinkable material because it is excellent in heat resistance and resistance after bonding. S ' contains a domain-hardening resin. Epoxy is the ring of the main component, and the second agent can be used for short-term hardening and good workability, and the molecular beding agent is better in characteristics. In addition, the radical hardening type is followed by a lower temperature of the agent. The characteristics such as excellent curability can be appropriately selected depending on the application. The oxygen-based secondary shaft is made of a thermosetting material such as an epoxy resin and a chemical agent such as the item 12 201139259. In addition, a thermoplastic resin or a coupling agent is usually blended as needed. , Filler, etc. The above-mentioned epoxy resin may, for example, be a bisphen A epoxide, a bisphen 〇 1 F epoxy resin, or a double s (8) ring. Oxygen resin, benzene _ (phen0ln0V0lac) ^• epoxy fine Θ, A riding acid (_Q1 nQVGlae) type epoxy resin, double age A secret (bisphen〇1 An〇v〇lac) type epoxy resin, gamma F _ iTr\Fnovolac) ^ Glycidyl ester epoxy resin, Glycidyl rm oxy-resin, ethyl endoenzyme (h fine 0in) type epoxy resin, t (lS; cyanurate>, a. k some epoxy resins can be _, can also be hydrogenated. In addition, == brewing base or Methyl propylene is added to the side chain of the epoxy resin. ~Epoxy resin can be used alone or in combination of two or more. If the hardener can harden the epoxy resin, it will be hardened. Agent, = ionic polymerizability __ hard tilting, hardening in polyaddition, excellent in quick-curing property, no need for chemical equivalent considerations, and L' is preferably anionic or cationically polymerizable catalyst-type hardening Listed as a cation or a cationically polymerizable catalyst-type hardener, for example, lmldazoIe, hy (hyd ::, amine salt, diazomum salt, aliphatic salt Et,) 13 201139259 amine imide, diammine maleimide, melamine and its derivatives, polyamine salts, dicyandiamide ( Such as dicyandiamide), etc., it is also possible to use modified substances of these compounds, etc. Examples of the curing agent include polyamines, polythiols, polyphenols, acid anhydrides, etc. The curing agents of these epoxy resins are polyamino phthalate esters. A polymer material such as a polyester, a metal thin film such as nickel or copper, or an inorganic material coated with an inorganic material such as a sulphuric acid or the like, which is microencapsulated, is preferred because it can be used for a long period of time. These hardeners may be used alone or in combination of two or more. The amount of the above-mentioned hardening agent is usually from about 5 parts by mass to about 20 parts by mass based on the total amount of the thermosetting material and the thermoplastic resin to be blended as needed. The radical-curable adhesive is, for example, a radical polymerizable material and a radical polymerization S-starting agent. Further, a thermoplastic resin, a coupling agent, a filler, and the like are usually formulated as needed. The radically polymerizable material can be used without limitation as long as it is, for example, a substance having a functional group polymerized by a radical. Specific examples include, for example, a lactic acid acrylate (including a corresponding methyl acetoacetate, the same applies hereinafter) a compound, a propylene sulfhydryl group (including a corresponding methyl propylene oxide oxy group or lower) compound, Cis-butadiene di-imine (de-maize W) 4 : a radically polymerizable substance such as a methyl cis-butanimide (c) (reagent (10)) resin, nadimide resin. These 201139259 radical polymerizable substances may be used in the form of a monomer or a polymer, or may be used in combination with a monomer. Examples of the above acrylate compound include methyl acrylate, ethyl acrylate, isopropyl acrylate, isobutyl acrylate, and ethylene glycol diacrylate. (ethyleneglycol diacrylate), diethyleneglycol diacrylate, trimethylolpropane triacrylate, tetramethylolmethane tetraacrylate 2-Hydroxy-1,3-diacryloxypropane, 2,2-bis[4-(acryloxymethoxy)phenyl]propane 2,2-bis[4-(acryloxymethoxy)phenyl]propane ), 2,2-bis[4-(acryloxypolyethoxy)phenyl]propane (2,2_bis[4-(acryl〇xy polyethoxy) Phenyl]propane), dicyclopentenyl acrylate, tricyclodecanyl acrylate, tris(acryloyloxyethyl)isocyanurate ), urethane urate (urert) Ianeacrylate) and so on. Further, a polymerization inhibitor such as hydroquinone or methyiettler hydroquinone may be suitably used as needed. In addition, from the viewpoint of the improvement of heat resistance, a radically polymerizable substance such as an acrylate compound preferably has at least one substituent such as a dicyclopentenyl group, a tricyclodecanyl group or a triazine ring. The radically polymerizable substance other than the acrylate compound may be, for example, a compound described in International Publication No. 2009/063827. These compounds may be used alone or in combination of two or more. The above-mentioned radical polymerization initiator can be used without particular limitation as long as it is a compound which decomposes to generate free radicals by, for example, heating or light irradiation. Specifically, for example, a peroxidic compound, an azo compound, or the like can be mentioned. Such a hardener can be appropriately selected depending on the target connection temperature, connection time, use period, and the like. More specifically, the radical polymerization initiator may be exemplified by diacyl peroxide, peroxydicarbonate, peroxyacetic acid (per0Xyest; er), peroxyketal, Dialkylperxide, hydroperoxide, siiyi peroxide, and the like. Among these radical polymerization initiators, peroxy esters, dialkyl peroxides, hydroperoxides, decyl peroxides and the like are preferred, and more preferred peroxyesters are obtained. As the radical polymerization initiator, for example, a compound described in International Publication No. 2009/063827 can be suitably used. These radical polymerization initiators may be used alone or in combination of two or more. The amount of the above-mentioned radical polymerization initiator is usually from 0.1 part by mass to about 1 part by mass based on 100 parts by mass of the total amount of the radical polymerizable material and the thermoplastic resin to be blended as needed. The thermoplastic resin to be blended as needed in the epoxy-based adhesive and the radical-curable adhesive is, for example, a resin which is easy to impart a film property to the adhesive. Examples of the thermoplastic resin include a phenoxy group (phen〇Xy). Resin, polyvinyl formal resin, polystyrene 16 201139259. (polystyrene) resin, polyvinyl butyral (p〇iyVinyi butyral) resin, polyester resin, polyamide resin, xylene resin , polyamino phthalic acid resin, polyacetic acid vinegar resin, enamel resin, terpene phenol resin and the like. As the thermoplastic resin, for example, a compound described in International Publication No. 2009/063827 can be suitably used. Among these compounds, a phenoxy resin is preferred in terms of excellent properties such as adhesion, compatibility, heat resistance, and mechanical strength. These resins may be used alone or in combination of two or more. In the case of being blended in an epoxy-based adhesive, the amount of the thermoplastic resin is usually from 5 parts by mass to about 80 parts by mass based on 1 part by mass of the total amount of the thermoplastic resin and the thermosetting material. In the case where the thermoplastic resin is blended in the radical-curable adhesive, the amount of the thermoplastic resin is usually from 5 parts by mass to 80 parts by mass based on the total mass of the thermoplastic resin and the radical polymerizable material. By winding the anisotropic conductive tape 5 around the core 1 in such a manner that the substrate 6 faces inward, an adhesive having a relatively low viscosity and which is prone to agglomeration in the prior art can be used in the adhesive layer. The subsequent layer 8 may have a shear viscosity of 3 Å < t of 100000 Pa.s or less. The viscosity is preferably 1 〇〇〇 Pa s~ 50000 Pa_s, and more preferably 1000 Pa.s~3 〇〇〇〇卩. The low-viscosity adhesive component 8a is a thermal radical-curable adhesive, and a low-temperature curing type adhesive is exemplified. Specific examples thereof include a thermal radical curing type adhesive containing a radical polymerization initiator having a 丨 minute half-life temperature of 16 or less. The i-minute half-life temperature is more preferably a machine 丨 丨 thief, and particularly preferably _ 〜 l2 〇 (>c. Such a hardener is exemplified by: T. ternary hexaoxyperoxide hexaphthalate terephthalic acid brewing 17 201139259 (1 minute half-life temperature: 142 ° C, HTP-65W manufactured by Kayaku Akzo Co., Ltd. (trade name)), substituted amber-based peroxide (1 minute half-life temperature: 13 U 〇 C, manufactured by Nippon Oil Co., Ltd., Nyper BMT (trade name)), February lauric acid peroxide ( 】 Minute half-agricultural temperature: 116.4 ° C 'Manufactured by Nippon Oil & Fat Co., Ltd., Peroyl L (trade name)), etc. Other examples of the low-grade adhesive component 8a include a thermoplastic resin and 30. a free radical polymerizable material and a thermal radical curing type binder of a radical polymerization initiator; the content of the above radical polymerizable substance in the thermal radical curing type binder is relative to thermoplastic The total amount of the fat and the radical polymerizable material is 1 part by mass, preferably 20 parts by mass to 80 parts by mass. The content is more preferably 3 parts by mass to 80 parts by mass 'more preferably 4 parts by mass to 8 parts by mass. The binder component 8a may be an epoxy binder containing a thermoplastic resin, a thermosetting material containing a liquid epoxy resin, and a curing agent. In this case, an epoxy-based adhesive is used. The content of the epoxy resin is preferably 2 parts by mass to 8 parts by mass, based on the total amount of the thermoplastic resin and the thermosetting material, and is preferably 2 parts by mass to 8 parts by mass. The mass portion is particularly preferably 30 parts by mass to 80 parts by mass. Further, when the 1C wafer is mounted on a glass substrate or a flexible printed circuit board (FPC), the difference in the coefficient of linear expansion between the wafer and the substrate is self-suppressed. In view of the warpage of the substrate to be produced, it is preferable that a component that exhibits a relaxation effect of internal stress is blended in the adhesive component. Specifically, it is preferable to blend an acrylic rubber or an elastomer component into the adhesive component. Another 18 ii201139259 ^Type^::Use as country The radical hard metal described in the publication No. 98/44067 may, for example, be a ceramic such as Au, Ag, Ni, Cu, or a solder, or may be a non-conductive glass, ceramic, or material. The core is coated with a film of the above metal or carbon on the core, or metal or thermally melted. If the conductive particles 8b are made of plastic, the conductive particles can be deformed when the connector is heated and pressurized. When the contact area of the 0-electrode electrode and the conductive particle 8b is increased, the surface of the conductive particle 8b can be added and the "two (10) edge particles of the polymer tree can be added. By adding the insulating particles, the amount of the particles is increased. Case ' When used as an anisotropic conductive tape, the short circuit caused by the particles can be suppressed, and the adjacent circuit electrodes can be improved. Further, it can be selected from insulating particles and conductive particles! Or use two types of particles in combination. The average particle size of the conductive particles and the insulating particles is preferably from 1 μΠ1 to 18, more preferably from 2.5 μm to 10 μιη, in terms of dispersibility and goodness. The blending amount of the sub- 8b is not particularly limited. When the adhesive composition is based on 2, it is preferably W% by volume to 3G, more preferably (Π /〇~10% by volume, particularly preferably 〇5% by volume). 5% by volume. If the amount of the conductive $8b is less than 〇]% by volume, there is an excellent conductivity, and if it exceeds 3.5% by volume, the domain is short-circuited by the circuit when the phase is in the intestinal conductive band. In order to reduce the fluidity of the adhesive layer 8, the inorganic filler may be adjusted to the adhesive component 8a in accordance with 201139259. The inorganic filler is not particularly limited as long as it is, for example, a solid particulate inorganic compound. Specific examples of the material include, for example, water hydroxide IS, magnesium hydroxide, carbonated water, carbonic acid town, Shixi acid office, Shixi acid town, oxidation word, oxidation town, oxidation Ming, nitrite, and occupational aluminum. The aluminum borate whisker, the boron nitride, the crystalline cerium oxide, or the amorphous dioxide dioxin, the cerium oxide, etc. may be used singly or in combination of two or more. In the present embodiment, the substrate 6 is oriented The core side (inside) manner is such that the anisotropic conductive strip 5 is pure to the core 丨±, that is, the material is dispensed in the adhesive layer 8 or even if the volume is set to 1 based on the volume of _ 8 20% by volume or less can also sufficiently suppress agglomeration. The content of the inorganic filler is more preferably from 0% by volume to 15% by volume, particularly preferably from 0% by volume to 1% by volume. Further, even if the amount of the adhesive layer 8 is f 4 t mass 5G mass can be used to suppress agglomeration. Inorganic = 3 is more preferably G mass % ~ 4G f %, especially preferably G mass % ~ 3 tannin, %. The content of the mass base is preferably a suitable layer depending on the inorganic filler to be used: the case where the material is cerium oxide, even if it is based on the mass of the adhesive agent 4 is set to % f by % or less, and may be sufficiently agglomerated. The content of the cerium oxide is preferably 〇% by mass to 3% by mass, especially two parts by weight of I2 2G. The inorganic filler is oxidized 18 In the case of 'the content of the mass of the following 8 is set to 5〇 mass%, the underarm' can also sufficiently suppress the oxygen content of the knot I. Good for G mass%~ 20 201139259 & 40% by mass, especially for 〇% by mass%~3〇% by mass. Next, it can be calculated as 'but in self-determination. For the case of Dingxu, for example, the electric furnace can be measured by the following method (The temperature of the air ring is raised to the temperature of the shoe first and then heated for 45 minutes. The dense electronic balance measuring the content of the filler, the fine ru^, τ produced by the manufacturer, and the decimal point (0.0 〇U) are measured. Bodhisattva (4)% Γ上玫去撕撕' The bribe is turned over from the adhesive tape and placed on the carrier layer about 1 g. The material ' _ amount is carried out in 23 machines, stupid, 1 atmosphere. (4) will join The crucible having the adhesive layer was heated in an electric furnace for 45 minutes in the same manner as (1). By this heating, _ becomes ash. (5) The temperature of the electric furnace was returned to the normal temperature, and the mass of the crucible and the ash taken out from the electric furnace were quickly weighed in the same manner as in the above (2) and (3) in the drier. (6) The mass of the ash obtained in (2) is subtracted from the mass of the 坩埚 and ash obtained in (5), and the mass of the ash is calculated. The ash should contain inorganic fillers and conductive particles (metal components). (7) The type and content of the conductive particles (metal components) contained in the ash are calculated by Inductively Coupled Plasma (ICP) luminescence spectrometry. At this time, the ash is decomposed by the mixed acid of argon fluoride acid and nitrate 21 201139259 acid to prepare the supply.

(ICP-AES 屬種類及其含量進行定量分析。上的金 酸及水以質量比i: i: 1混合酸、石肖 灰分的質量中減去上述利用 =6=獲得的 電粒子(金W八„ 先77析法算出的導 成/7 )的質量’作為無機填料的質量。 *»,p 乾式比重6丨(島津製作所,乾式密 系列)敏㈣财取出的灰分的=、 ==著劑層的比重,將利用1cp發光分光分析法 檢測出的金屬的理論比重及含4自灰分 填料相對於原本接著劑層的體積百分比。算出-機 為了製作接著材捲筒10’例如可首先將含有接著劑成 分的塗佈液塗佈於基材膜(可使用上述各種材料作為基 材,例如聚對苯二曱酸乙二賴)上等,製作異向導電二 的整幅材料β將該整幅材料以成為適合於用途的寬度的方 式裁斷為帶狀。該裁斷時可使用例如日本專利特開 2003-285293號公報所記載的分割裝置。藉由將成為預定 寬度的異向導電帶5捲取於捲筒零件的捲芯上而製造接著 材捲筒10。此時’本實施形態中,以基材6朝向捲芯1側 且接著劑層8朝向外侧的方式將異向導電帶5捲取於捲芯 1上。 本發明中為了將異向導電帶捲取於捲筒零件的捲芯 上’較佳為將異向導電帶的最初部分(捲繞開始的部分) 22 201139259 固定在捲芯上而觀。該固定方法可使用眾所周知的方 ^ ’例如可利用黏著帶、黏著劑來固定。另外,亦可於捲 ^上設置卡具或切口部來固定。其中,就作業性的觀點而 S,較佳為使用黏著帶或黏著劑來固定。 此外,於異向導電帶5的捲重體的外周露出接著劑層 8’為了使該部分不會被塵埃等污染,而視需要謀求如下所 述的對策。例如’對異向導電帶5的最後部分(捲繞結束 的。卩分)預先去除基材6上的接著劑層8而設置空白部分, 將其纏繞於捲重體上,藉此可防止接著劑層8的露出。或 者,亦可代替於基材6上設置空白部分而準備其他帶(可 ^不與基材相_帶),將其連接於基材6的端部而纏繞於 +重體上。除上述以外,亦可藉由將接著材捲筒1〇放入袋 中保存而抑制來自外部環境的污染。 (電路連接體) 接著,對將本實施形態的接著材捲筒1〇的接著劑層8 ,作電路連接材料而製造的電路連接體進行說明。圖5所 ,的電路連接體1〇〇具備相互對向的第一電路構件3〇及第 一電路構件40,且於第一電路構件3〇與第二電路構件4〇 之間設置有連接該些構件的連接部5〇a。 第一電路構件30具備電路基板31、及形成於電路基 板31的主面31a上的電路電極32。第二電路構件40具備 電路基板41、及形成於電路基板41的主面41a上的電路 電極42。 電路構件的具體例可列舉半導體晶片(IC晶片)、電 23 201139259 阻器B曰片、電谷器晶片等晶片零件等。該些電路構件具備 電路電極’通常具備多個(至少兩個以上)電路電極。、上 述電路構件所連接的另-個電_件的具體例可列舉:具 有金屬配_可撓性帶、可紐印刷配線板、蒸鍍有銦锡 ,化物(Indium Tin Oxide ’ IT0)的玻璃基板等配線基板。 藉由使用自接著材捲筒1〇上拉出的異向導電帶5,可有效 率且以高連接可靠性將電路構件彼此連接。因此,本實施 形態的異向導電帶5適合於具備多個微細連接端子(電路 電極)的晶片零件在配線基板上的c〇G安裝(Chip 〇n Glass)或者 COF 安裝(Chip0nFlex)。 各電路電極32、42的表面可由選自金、銀、錫、釕、 铑、鈀、锇、銥、鉑及銦錫氧化物(IT〇)中的丨種構成, 亦可由2種以上構成。另外,電路電極32、42的表面的材 質可於所有電路電極中相同,亦可不同。 連接部50a具備接著劑層8中所含的接著劑成分如 的硬化物8A、及分散於其中的導電粒子肋。而且,電路 連接體100巾’對向的電路電極32與電路電極42是經由 導電粒子8b而電性連接。即,導電粒子%直接接觸於電 路電極32、42兩者。 因此’電路電極32、42冑的連接電阻充分降低,電路 電極32、42間的良好電性連接成為可能。另一方面,硬化 物8A具有電氣絕緣性,鄰接的電路電極彼此的絕緣性得 到確保。因此,可使電路電極32、42間的電流的流動順利, 可充分發揮電路所具有的功能。 24 201139259 . .'a (電路連接體的製造方法) 法的一實施形態的步驟圖。本實施形能中連=造方 5的’最終製造電路連接帶 捲筒⑻順劑if朝上安裝接著材 上拉出異向導電帶5。2 式自該接著材捲筒U) 載置於電路構件30#主面^導電;"5切斷為預定長度而 接著,向圖二的H (圖6U))。 接著劑層8暫時固定於第:電路構,牛前3= f向加壓’將 此時的壓力只要是不對電 (圖6⑴)。 特別限制,通常較&A D 仏成知傷的範圍,則並無 邊加熱-邊加厂 化的溫度。加熱溫度通著劑層8實質上不硬 剝離基材6後,如圖6 (c) 42朝向第-電路構件3〇側)斤H第二電路電極 (C)的箭碩A及箭頭B方 圖 度是設為接著劑層8的接著f:f °此時的加熱溫 變慢的傾向,=於Γ,則存在硬化速度為 超8 C,則存在容易進行不期望的副 25 201139259^ 反應的傾向。加熱時間較佳為〇」秒〜180秒,更佳為〇 5 秒〜180秒,尤佳為1秒〜180秒。 . 藉由接著劑成分8a的硬化而形成連接部5〇a,獲得圖 5所示的電路賴體1GG。連接的條件是根據所使用的用 途、接著劑成分、電路構件而適當選擇。此外,於使用藉 由光而硬化的成㈣為麟_ 8的接著劑成分的情況f 只要對接著劑層8適當照射活性光線或能量線即可。活性 光線可列舉紫外線、可見光、紅外線等。能量線可列舉電 子束、X射線、γ射線、微波等。 依據本貫施形態,藉由以基材6朝向捲芯侧(内侧) ,方式將異向導電帶5捲繞於捲芯丨上,可於將捲繞於捲 筒零件上的異向導電帶5拉出時,以極高的水準抑接 劑層8自基材6上剝離。 曰以上,已對本發明的較佳實施形態進行說明,但本發 j並不限疋於上述貫施形態。本發明可於不脫離其要旨 範圍内進行各種變形。 、 例如,於上述實施形態中,已例示異向導電帶5作為 =連接㈣接著材帶,但亦可將接著綱8包含接著劑 ^分仏且不含導電粒子肋的非導電帶捲繞於捲芯!上來 ^乍接著材捲筒’亦可使用調配有比異向導電帶更多的導 ,輪子8b的不具異向性的導電帶。另外,亦可適宜用於黏 曰曰膜、銀膜、半導體晶圓加工用的接著臈等各種電子材料 用的接著膜。另外’於上述實施形態巾,已例示採用具有 肋狀結構部2b的側板2的情況,但亦可代替該側板2而使 26 201139259 肋狀結構部的;2b _板(參照圖7)。此種不具有 易產側板由於比上述具有肋狀結構部的側板更容 ^故而可藉由剌本發明而充分抑制結塊。 居祕π於上述實施形態中,已例示接著綱8包含一 ;示二桩?旦亦可於基材6上設置多層。例如,圖8 (a) # u s A者材帶15A具備多層結構的接著劑層18。接著劑 含導f粒子的導妹子非含有層18&及含有導 八;、導電粒子含有層18b所構成。此外,導電粒子非 ,及導電粒子含有層18b的接著舰分可使用與 述,讀層8的接著劑成分相同的成分。 若將上述兩層結構的接著劑層18用作電路連接材 則於電路構件彼此的_ 刀的流動引起的電路電極上的導電粒子個數的減少。因 如於將1C晶片藉由C0G安裝或者c〇F安裂而連接 」土板上的情況,可充分確保1C晶片的金屬凸塊上的導電 粒子的個數。此時,較佳為以IC晶片的具備金屬 ^導電粒子非含有層18a,以及可安裝1C晶片的基板與 電粒子含有層18b分別抵接的方式配置接著劑層18。/、 自更確實地防止接著劑層8的剝離的觀點考慮,圖8 (b)所示的接著材帶15B在基材6與接著劑層8之間茂 f有黏著劑層9a。自對電路構件的貼附性提高的觀 言,圖8(c)所示的接著材帶15C在接著劑層8上進·一 積層有黏著劑層9b。 [實例] 27 201139259 以下,利用實例對本發明 明並不限定於該些實例。 (實例1) 進行更詳細的說明,但本發 [接著劑成分的原材料的準備] 為了製作接著劑成分’而準備以下的原材料。 古阳具有熱塑性的苯氧基樹脂(uni〇n㈤此股份 司’ 商〇口名.pKHc,質量平均分子量 溶解於將甲,(彿點⑽处)與乙酸乙自旨(沸點771。〇 =1 1 (質量比)混合而成的混合溶劑中,製備固體成分 為40質量%的苯氧基樹脂溶液。 準備於30 C為液狀的丙烯酸胺基甲酸酯(新中村化學 工業股份有限公司製造,商品名:UA_512,質量平均分子 量· 2800)、以及於3〇。(:為液狀的二甲基丙烯酸醋(新中 村化學工業股份有限公司製造,商品名:Dcp,質量平均 分子量:332),來作為自由基聚合性物質。 準備二月桂醯基過氧化物(日本油脂股份有限公司製 造’商品名:Peroyl L,1分鐘半衰期溫度1164ΐ,質量 平均分子量:399),來作為產生游離自由基的硬化劑(自 由基產生劑)。 [接著材膜的製作] 使用如上所述準備的原材料,如下所述製作接著材膜。 相對於40質量份的苯氧基樹脂溶液,調配4〇質量份 的液狀丙烯酸胺基曱酸酯、20質量份的液狀二曱基丙歸酸 酯、4質量份的自由基產生劑而獲得混合液。對該混合液 28 201139259 調配平均粒_搜為5μηι的錄粉(導電粒子)、及平均粒徑為 0.5 μηι #二氧化石夕粉(無機填料),獲得於混合液中分散 有鎳粉及一氧化發粉的塗佈液。 使用塗佈裝置,以32〇m的長度將上述塗佈液塗佈於 厚度80 μηι、寬度5〇〇 mm且兩面經聚石夕氧脫模處理的pET 膜(載體膜)上,使用爐長15m、熱風溫度贼的乾燥爐, 以3 m/min的速度進行乾燥。藉此,獲得於ρΕτ膜的一面 上設置有接著劑層(厚度:4〇μιη)的接著材膜(全長32〇 m) 〇 乾燥後的接著劑層的鎳粉含量為15體積%,二氧化 矽粉含量為15體積% (26質量%)。 [剪切黏度的測定] 藉由將上述接著材膜的接著劑層(厚度:4〇 層 壓15片而製作厚度約〇.6 mm的接著劑層,將切割為i cmxl cm尺寸的材料作為試料,測定接著劑層的剪切黏 度。該測定時使用剪切黏彈性測定裝置(TA Instmments 公司製造,商品名:ARES)。其結果為,接著劑層的於3〇 °C的剪切黏度為20000 IVs。此外,測定條件為如下所述。 測定頻率:1〇 Hz ; 環境氣體:氮氣下; 溫度範圍:〇°C〜150°c ; 升溫速度:l〇°C/min ; 探針直徑:8 mm ; 試料尺寸:10 mmxlO mm ; 29 201139259 試料厚度:約0.6 mm ; 測定應變量:1.0%。 [接著材捲筒的製作] 利用輥對輥(roll to roll)的分割設備將上述接著材膜 裁斷為寬度1.5 mm,以300 m的長度將接著材帶捲取於捲 筒零件(捲芯外徑:66 mm,塑膠成型品)上。此時,以 包含PET的基材朝向捲芯側(内侧),且接著劑層朝向外 侧的方式捲取。於捲芯的兩側設置捲筒側板(厚度2〇 mm),該捲筒側板與接著材帶的捲重體之間的間隙距離為 左右分別約0.1 mm〜0.5 mm的範圍内。此外,本實例中 使用圖1所示的具有設置有放射狀地延伸存在的肋狀結構 部2b的捲筒側板的捲筒零件,但使用如圖7所示的具有未 設置放射狀地延伸存在的肋狀結構部的捲筒側板的捲筒零 件’亦獲得本發明的效果。 [關於接著劑層的剝離的有無的評價] 將上述接著材捲筒以於35。〇的恆溫槽内垂直靜置的 狀態放置24小時後’利用顯微鏡觀察侧_狀態。其結果 為’確認自捲重體賴φ滲$的接著獅接著於捲筒側板 上。接著’將該接著材捲筒以每秒〗m的速度進行全長綱 出試驗,結果接著劑層自基材上剝離的不U次亦 (實例2) [接著劑成分的原材料的準備] 為了製作接著劑成分,準備以下的原材料。 30 201139259 有限:以有商熱产::笨氧基樹脂(Uni°n c娜 冰商〇〇名^c,質量平均分子量:4500〇), 二二 <甲笨(彿點11〇.6£>C)與乙酸乙醋(沸點77.rC) 1 · 1 (督署^ μμ、 人 ’ 主)混合而成的混合溶劑中,製備固體成分 *'''質里〇/〇的笨氧基樹脂溶液。 阳八^t 3G°C為液狀的環氧樹脂(日本環氧樹脂股份有 二Λ二商名:孔_環氧當量:180〜19〇)、及 ^ 心的環氧樹脂(曰本環氧樹脂股份有限公司製 Ϊ樹: 1G32H6() ’環氧當量:163〜175) ’來作為環 準備芳麵㈣(三新化學工業股份有限公司製造, 商品名:SI·60)’來作為環氧樹脂的硬化劑。 [接著材臈的製作] 使用如亡所述準備的原材料,如下所述製作接著材膜。 ,對於苯氧基樹脂溶液35質量份,調配6〇質量份的 於”液狀的環氧樹月旨YL-980、5質量份的於30。。為 ,I、的環氧樹脂1032H60、及4質量份的硬化劑SI-60,獲 得混合/液。對該混合液調配平均粒徑為5 μπι的鎳粉 '及 平均粒徑為G.5 的二氧化雜,麟於混合液中分散有 鎳粉及二氧化矽粉的塗佈液。 使用塗佈裝置,以320m的長度將上述塗佈液塗佈於 厚度80 μιη、寬度500 mm且兩面經聚矽氧脫模處理的ρΕτ 膜上’使用爐I 15m、熱風溫度7〇°C的乾燥爐以3m/mm 的速度進行乾燥。藉此,獲得於PET膜的一面上設置有接 201139259 著劑層(厚度:40 μπΟ的接著材膜(全長320 m)。 乾燥後的接著劑層的鎳粉含量為1.5體積%,二氧化 碎粉含量為15體積% (26質量%)。 [剪切黏度的測定] 以與實例1相同的方式測定上述接著材膜的剪切黏 度’結果接著劑層的於30。(:的剪切黏度為loooo pa.s。 [接著材捲筒的製作] 以與實例1相同的方式裁斷上述接著材膜,並且以所 付的接考材帶的基材朝向捲芯側(内側),且接著劑層朝向 外側的方式將上述帶捲取於捲筒零件(塑膠成型品)上。 藉此,獲得捲繞有寬度1.5 mm、長度300 m的接著材帶的 接著材捲筒。捲筒侧板與接著材帶的捲重體之間的間隙距 離為左右分別約〇1 mm〜〇 5 mm的範圍内。 [關於接著劑層的剝離的有無的評價] 將上述接著材捲筒以於35eC的恆溫槽内垂直靜置的 狀態放置24小時後,利用顯微鏡觀察側面的狀態。其結果 為’確,自捲重體賴面滲出的接著麵接著於捲筒侧板 上。接著,將該接著材捲筒以每秒丨m的速度進行全長3⑻ 的抽出試驗’結果接著綱自基材上剝離的不良1次亦 禾產生。 (實例3) 首先,以與實例丨相_方式製作接著材捲筒。由於 ,者劑容易自捲重體的侧面滲出,故而除了於接著的 則端設置5G g的錘來對捲重體整體施加捲緊的張力以 32 201139259 外,與實例1同樣地以於恆溫槽内垂直靜置的狀態放置24 小時。其後,利用顯微鏡觀察側面的狀態,結果確認自捲 重體的側面滲出的接著劑黏接著於捲筒侧板上。接著,將 該接著材捲筒以每秒1 „!的速度進行全長3⑻㈤的抽出試 驗,結果接著劑層自基材上剝離的不良i次亦未產生。 (實例4) 除了代替以與實例1相同的方式製作的接著材捲筒, 而使用以與實例2相同的方式製作的接著材捲筒以外,與 實例3同樣地於接著材帶的前賴置% g的錘㈣接著材 捲筒放置練溫槽内。其後,顯微鏡觀察㈣的狀態, 結果確認自捲重體_面滲出的接著齡接著於捲筒侧板 上接著’將該接著材捲筒以每秒1〇1的速度進行全長3〇〇 m的抽出試驗,結果接㈣丨層自基材上_的不良i次亦 未產生。 (實例5) 除了對以與實例1相同的方式製作的接著材捲筒,將 怪溫槽的溫度設定為贼來代替設定為饥以外,與實例 1同樣地雜料騎放置純溫槽内。錢,利用顯微 鏡觀察側面的狀態,結果確認自捲重體的側面滲出的接著 劑黏接著於捲筒側板上。接著,賴接著材捲筒以每秒i m 的速度進仃全長3GGm的抽出試驗,結果接著劑層自基材 上剝離的不良1次亦未產生。 (比較例1) 除了以基材朝向外側’且接著劑層朝向捲怒側(内側) 33 201139259 的方式將接著材帶捲取於捲芯上以外,以與實例i相同的 方式製作接著材捲筒,以於35°C的恆溫槽内垂直靜置的狀 態放置24小時。其後’利用顯微鏡觀察側面的狀態,結果 確認自捲重體的侧面滲出的接著劑黏接著於捲筒侦|板^。 接著’將該接著材捲筒以每秒1 m的速度進行全長3〇〇 m 的抽出試驗,結果接著劑層自基材上剝離的不良產生15 次。 (比較例2) 除了以基材朝向外側,且接著劑層朝向捲芯側(内側) 的方式將接著材帶捲取於捲芯上以外,以與實例2相同的 方式製作接著材捲筒,以於35°C的恆溫槽内垂直靜置的狀 態,置24小時。其後,利用顯微鏡觀察側面的狀態,結果 確,自捲重體的側面滲出的接著劑黏接著於捲筒側板上。 接著,將該接著材捲筒以每秒丨m的速度進行全長3〇〇瓜 =抽出試驗,結果接著劑層自基材上剝離的不良產生17 次。 雖然本㈣已讀佳實施_露如上,财並非用 2本發明’任何熟習此技藝者,在不脫離本發明之泰 範當可作些許之更動與潤飾,因此本發明之辆 ,圍當視伽之申請專__界定者為準。 【圖式簡單說明】 圖。圖1是表示本發_接著材觸的—實施形態的立體 圖2疋不讀表示圖i所示的接著材㈣的内部結構 34 201139259 _____Γιτ 的剖面圖。 圖3是表示本發明的接著材捲筒的侧板的内側面 面圖。 圖4疋示思性表示異向導電帶的一例的剖面圖。 圖5是示思性表示電路電極彼此連接的電路連接 一例的剖面圖。 ' 圖6(a)〜圖6(c)是示意性表示電路連接體的製造方 的一例的剖面圖。 ' 圖 體圖 圖8(a)〜圖8(c)是示意性表示異向導電帶的其他例子 的剖面圖。 圖9疋不意性表示自先前的接著材捲筒上拉出接著材 可時所產生的結塊的一例的剖面圖。 【主要元件符號說明】 7是表示本發明的接著材捲筒的其他實施形態的立 1 :捲芯 2 =側板 2a :貫通孔 2b :肋狀結構部 5:異向導電帶(接著材帶) 6 ' 26 :基材 8 ' 18、28 :接著劑層 8A ·硬化物 8a :接著劑成分 35 201139259. 8b :導電粒子 9a、9b :黏著劑層 10 :接著材捲筒 10a :軸孔 10b :缺口部 15A、15B、15C、25 :接著材帶 18a :導電粒子非含有層 18b :導電粒子含有層 30 :第一電路構件 31、 41 :電路基板 31a、41a :主面 32、 42 :電路電極 40 :第二電路構件 50a :連接部 100 :電路連接體 A、B .前頭 F1 :外表面 F2 :内側面 36(Quantitative analysis of the genus and its content of ICP-AES. The gold acid and water on the mass ratio i: i: 1 mixed acid, stone ash ash minus the above-mentioned use = 6 = obtained electric particles (Gold W The quality of the inorganic filler is calculated as the mass of the inorganic filler. *»,p The dry specific gravity is 6丨 (Shimadzu Corporation, dry-type dense series) Min (4) The ash of the money is taken =, == The specific gravity of the agent layer, the theoretical specific gravity of the metal detected by the 1 cp luminescence spectrometry and the volume percentage of the ash-containing filler relative to the original adhesive layer. The calculation machine may firstly The coating liquid containing the adhesive component is applied to a substrate film (the above various materials can be used as a substrate, for example, polyethylene terephthalate), and the entire material β of the opposite conductive material is produced. The entire material is cut into a strip shape so as to be suitable for the width of the application. For the cutting, for example, a dividing device described in Japanese Laid-Open Patent Publication No. 2003-285293 can be used, by using an anisotropic conductive tape 5 having a predetermined width. Roll taken from the roll part In this embodiment, the counter conductive tape 5 is wound around the winding core 1 so that the base material 6 faces the winding core 1 side and the adhesive layer 8 faces outward. In the invention, in order to wind the anisotropic conductive tape on the core of the reel part, it is preferable to fix the initial portion (the portion where the winding starts) 22 201139259 of the anisotropic conductive tape to the core. A well-known method can be used, for example, by an adhesive tape or an adhesive. Alternatively, a clip or a notch can be provided on the roll to fix it. Among them, it is preferable to use adhesiveness from the viewpoint of workability. In addition, the adhesive layer 8' is exposed on the outer periphery of the weight body of the anisotropic conductive tape 5 so that the portion is not contaminated by dust or the like, and the following measures are required as needed. For example, The adhesive layer 8 on the substrate 6 is previously removed from the last portion of the anisotropic conductive tape 5 (the end of the winding), and a blank portion is provided, which is wound around the weight body, thereby preventing the adhesive layer 8 is exposed. Alternatively, it can be substituted for the substrate 6 A blank portion is provided to prepare another tape (which may not be associated with the substrate), and is attached to the end of the substrate 6 to be wound around the + heavy body. In addition to the above, the laminate can also be rolled 1 〇 〇 〇 保存 保存 ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( The circuit connector 1A of FIG. 5 includes a first circuit member 3A and a first circuit member 40 opposed to each other, and is disposed between the first circuit member 3A and the second circuit member 4A. The connection portion 5A is connected to the members. The first circuit member 30 includes a circuit board 31 and circuit electrodes 32 formed on the main surface 31a of the circuit board 31. The second circuit member 40 includes a circuit board 41 and a circuit electrode 42 formed on the main surface 41a of the circuit board 41. Specific examples of the circuit member include a semiconductor wafer (IC wafer), a wafer component such as a resistor 23, a semiconductor chip, and an electric grid wafer. These circuit members are provided with circuit electrodes', and usually have a plurality of (at least two or more) circuit electrodes. Specific examples of the other electric component to which the above-mentioned circuit member is connected include a metal-containing flexible tape, a switchable printed wiring board, and a glass in which indium tin oxide (IT0) is deposited. A wiring board such as a substrate. By using the anisotropic conductive tape 5 drawn from the backing roll 1 , the circuit members can be connected to each other efficiently and with high connection reliability. Therefore, the anisotropic conductive tape 5 of the present embodiment is suitable for c〇G mounting or COF mounting (Chip0nFlex) of a wafer component including a plurality of fine connection terminals (circuit electrodes) on a wiring substrate. The surface of each of the circuit electrodes 32 and 42 may be composed of a metal selected from the group consisting of gold, silver, tin, antimony, bismuth, palladium, iridium, iridium, platinum, and indium tin oxide (IT〇), or may be composed of two or more kinds. Further, the material of the surface of the circuit electrodes 32, 42 may be the same or different in all of the circuit electrodes. The connecting portion 50a includes a cured product 8A such as an adhesive component contained in the adhesive layer 8, and conductive particle ribs dispersed therein. Further, the circuit electrode 32 opposed to the circuit connector 100 and the circuit electrode 42 are electrically connected via the conductive particles 8b. That is, the conductive particles % are in direct contact with both of the circuit electrodes 32, 42. Therefore, the connection resistance of the circuit electrodes 32, 42A is sufficiently lowered, and a good electrical connection between the circuit electrodes 32, 42 is possible. On the other hand, the cured product 8A is electrically insulating, and the insulation of the adjacent circuit electrodes is ensured. Therefore, the flow of the current between the circuit electrodes 32 and 42 can be made smooth, and the function of the circuit can be sufficiently exhibited. 24 201139259 . . 'a (Method of Manufacturing Circuit Connector) A step diagram of an embodiment of the method. In the present embodiment, the final manufacturing circuit connecting tape reel (8) is used as the splicing agent, and the counter conductive tape 5 is pulled up from the upper mounting foil. The type is loaded from the bonding material U). The circuit member 30# main surface is electrically conductive; "5 is cut to a predetermined length and then to H (Fig. 6U) of Fig. 2). The subsequent agent layer 8 is temporarily fixed to the first circuit structure, and the front 3 = f is pressurized. The pressure at this time is not electrically connected (Fig. 6 (1)). Special restrictions, usually less than &A D 知 知 的 的 , , , , , , , 知 知 。 。 。 。 。 。 。 。 。 。 。 。 After the heating temperature agent layer 8 is substantially not hardly peeled off the substrate 6, as shown in Fig. 6 (c) 42 toward the side of the first circuit member 3), the arrow A and the arrow B of the second circuit electrode (C) The degree of heating is such that the heating temperature of the adhesive layer 8 is f:f°, and the heating temperature becomes slow. If the curing rate is higher than 8 C, the undesired secondary reaction is likely to occur. Propensity. The heating time is preferably 〇 sec to 180 sec, more preferably 〇 5 sec to 180 sec, and particularly preferably 1 sec to 180 sec. The connecting portion 5a is formed by hardening of the adhesive component 8a, and the circuit body 1GG shown in Fig. 5 is obtained. The conditions for the connection are appropriately selected depending on the use, the adhesive composition, and the circuit member to be used. Further, in the case where the (four) which is hardened by light is used as the adhesive component of the lining agent 8, the active light ray or the energy ray may be appropriately applied to the adhesive layer 8. Examples of the active light include ultraviolet light, visible light, infrared light, and the like. Examples of the energy line include an electron beam, X-rays, γ-rays, microwaves, and the like. According to the embodiment, the anisotropic conductive tape 5 is wound on the core rim by the substrate 6 toward the core side (inner side), and the anisotropic conductive tape wound on the reel part can be used. When the film is pulled out, the layer 8 is peeled off from the substrate 6 with an extremely high level. The preferred embodiments of the present invention have been described above, but the present invention is not limited to the above-described embodiments. The present invention can be variously modified without departing from the spirit and scope of the invention. For example, in the above embodiment, the anisotropic conductive tape 5 has been exemplified as a connection (four) adhesive tape, but a non-conductive tape including a bonding agent and a conductive particle rib may be wound around Core! Up, the 乍 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 Further, it can be suitably used for an adhesive film for various electronic materials such as an adhesive film, a silver film, or a semiconductor wafer. Further, in the above-described embodiment, the case where the side plate 2 having the rib-like structure portion 2b is used has been exemplified, but the 2b-plate (see Fig. 7) of the rib-like structure portion may be replaced by the side plate 2 instead of the side plate 2. Such a non-producible side panel can sufficiently suppress agglomeration by the present invention because it is more versatile than the side panel having the rib-like structure portion described above. In the above embodiment, it has been exemplified that the following 8 includes one; It is also possible to provide a plurality of layers on the substrate 6. For example, FIG. 8(a) #u s A material tape 15A has an adhesive layer 18 having a multilayer structure. The subsequent composition is composed of a non-containing layer 18& and a conductive layer-containing layer 18b. Further, the conductive particles are not used, and the subsequent components of the conductive particle-containing layer 18b can be the same as those of the adhesive layer of the read layer 8. When the above-described two-layered adhesive layer 18 is used as a circuit connecting material, the number of conductive particles on the circuit electrodes caused by the flow of the _knife between the circuit members is reduced. For example, when the 1C wafer is connected to the earth plate by C0G mounting or c〇F cracking, the number of conductive particles on the metal bump of the 1C wafer can be sufficiently ensured. In this case, it is preferable that the adhesive layer 18 is disposed such that the metal-containing conductive particle-containing layer 18a of the IC wafer and the substrate on which the 1C wafer can be mounted are in contact with the electrode-containing layer 18b. / From the viewpoint of more reliably preventing the peeling of the adhesive layer 8, the adhesive tape 15B shown in Fig. 8 (b) has an adhesive layer 9a between the substrate 6 and the adhesive layer 8. From the viewpoint of improved adhesion of the circuit member, the adhesive tape 15C shown in Fig. 8(c) has an adhesive layer 9b laminated on the adhesive layer 8. [Examples] 27 201139259 Hereinafter, the present invention is not limited to the examples by way of examples. (Example 1) Although the preparation of the raw material of the adhesive component is prepared in detail, the following raw materials are prepared in order to produce the adhesive component. Guyang has a thermoplastic phenoxy resin (uni〇n (five) this share division' Shangyukou name. pKHc, the mass average molecular weight dissolved in A, (Bu (10)) and acetic acid B (boiling point 771. 〇 = 1) A phenoxy resin solution having a solid content of 40% by mass is prepared in a mixed solvent of 1 (mass ratio). Prepared in a 30 C liquid urethane urethane (manufactured by Shin-Nakamura Chemical Co., Ltd.) , trade name: UA_512, mass average molecular weight · 2800), and 3 〇. (: liquid dimethyl acrylate vinegar (manufactured by Shin-Nakamura Chemical Co., Ltd., trade name: Dcp, mass average molecular weight: 332) , as a radically polymerizable substance. Prepared as a free radical to produce a ruthenium-based peroxide (manufactured by Nippon Oil & Fat Co., Ltd., trade name: Peroyl L, 1 minute half-life temperature: 1164 ΐ, mass average molecular weight: 399) Hardener (free radical generator) [Production of Substrate Film] Using the raw material prepared as described above, a film of a film was produced as follows. Relative to 40 parts by mass of benzene. The base resin solution was prepared by dissolving 4 parts by mass of liquid acrylamide phthalate, 20 parts by mass of liquid dimercaptopropionate, and 4 parts by mass of a radical generator to obtain a mixed solution. 28 201139259 Mixing average particles _ search for 5μηι recording powder (conductive particles), and an average particle size of 0.5 μηι #二氧化石夕粉 (inorganic filler), obtained by dispersing nickel powder and oxidized hair powder in the mixture The coating liquid was applied to a pET film (carrier film) having a thickness of 80 μm and a width of 5 mm and both sides of which were subjected to polyoxo oxygen release treatment using a coating apparatus at a length of 32 μm. Drying was performed at a speed of 3 m/min using a drying furnace having a furnace length of 15 m and a hot air temperature thief. Thereby, a backing film having an adhesive layer (thickness: 4 〇 μηη) provided on one surface of the ρΕτ film was obtained ( The total thickness of the adhesive layer after drying is 15% by volume, and the content of nickel powder of the dried adhesive layer is 15% by volume, and the content of cerium oxide powder is 15% by volume (26% by mass). [Measurement of Shear Viscosity] By using the above-mentioned adhesive film Adhesive layer (thickness: 4 〇 laminate 15 pieces to make thickness about 〇 A .6 mm adhesive layer was used as a sample to cut a material having a size of i cmxl cm, and the shear viscosity of the adhesive layer was measured. The shear viscoelasticity measuring device (manufactured by TA Instmments, trade name: ARES) was used for the measurement. As a result, the shear viscosity of the adhesive layer at 3 ° C was 20000 IVs. Further, the measurement conditions were as follows. Measurement frequency: 1 〇 Hz; Ambient gas: under nitrogen; Temperature range: 〇 ° C ~150 °c; heating rate: l〇 °C / min; probe diameter: 8 mm; sample size: 10 mm x lO mm; 29 201139259 sample thickness: about 0.6 mm; measured strain: 1.0%. [Preparation of the material roll] The above-mentioned film film was cut to a width of 1.5 mm by a roll to roll dividing device, and the backing tape was taken up to the roll part at a length of 300 m (outside the core) Diameter: 66 mm, molded on plastic). At this time, the substrate including PET was wound toward the core side (inner side), and the adhesive layer was taken up toward the outside. A roll side plate (thickness 2 mm) is disposed on both sides of the core, and the gap between the roll side plate and the roll weight of the backing tape is in the range of about 0.1 mm to 0.5 mm. Further, in the present example, the reel member having the reel side plate provided with the radially extending rib-like structural portion 2b shown in Fig. 1 is used, but has an extension extending radially as shown in Fig. 7 The reel part of the reel side plate of the rib structure portion also obtains the effects of the present invention. [Evaluation of the presence or absence of peeling of the adhesive layer] The above-mentioned binder roll was 35. After standing in a state in which the crucible was left standing vertically for 24 hours, the side_state was observed by a microscope. As a result, it is confirmed that the lion that has been infiltrated by the weight of the weight is attached to the side plate of the reel. Then, the full-length test was carried out at a rate of m per second, and the adhesive layer was peeled off from the substrate. (Example 2) [Preparation of raw materials for the adhesive component] Next to the ingredients, the following raw materials were prepared. 30 201139259 Limited: to have a hot product:: Stupid oxy-resin (Uni°nc Na ice merchant 〇〇 name ^c, mass average molecular weight: 4500 〇), two two < A stupid (Bud point 11 〇.6 £ >C) In the mixed solvent of ethyl acetate (boiling point 77.rC) 1 · 1 (supervised ^ μμ, human 'main), the solid component *''' Base resin solution. Yang Ba ^t 3G °C is a liquid epoxy resin (Japanese epoxy resin shares have two trade names: pore_epoxy equivalent: 180~19〇), and ^ core epoxy resin (曰本环Ϊ 氧 : : : : : : : : : : : : : : : : : : : : : 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 A hardener for oxyresin. [Preparation of the material] The raw material prepared as described above was used, and a film of the film was produced as follows. In an amount of 35 parts by mass of the phenoxy resin solution, 6 parts by mass of the liquid epoxy resin YL-980 and 5 parts by mass of the epoxy resin 1032H60, and 4 parts by mass of the hardener SI-60 to obtain a mixture/liquid. The mixture was prepared with a nickel powder having an average particle diameter of 5 μm and a carbon dioxide having an average particle diameter of G.5, which was dispersed in the mixed solution. Coating solution of nickel powder and cerium oxide powder. The coating liquid was applied to a ρ Ετ film having a thickness of 80 μm and a width of 500 mm and both sides of which were subjected to polyfluorination treatment by a coating apparatus using a coating apparatus. Drying was carried out at a speed of 3 m/mm using a furnace of furnace I 15 m and a hot air temperature of 7 ° C. Thereby, a laminate film of a thickness of 40 μπΟ (a thickness of 40 μπΟ) was provided on one side of the PET film. The total length of the adhesive layer after drying was 1.5% by volume, and the content of the pulverized powder was 15% by volume (26% by mass). [Measurement of Shear Viscosity] The same manner as in Example 1 was carried out. The shear viscosity of the above-mentioned adhesive film 'results in the adhesive layer at 30. (: The shear viscosity is loooo pa. s [Production of Substrate Reel] The above-mentioned adhesive film was cut in the same manner as in Example 1, and the substrate of the attached tape was oriented toward the core side (inside), and the adhesive layer was oriented outward. In the manner, the above tape is taken up on a reel part (plastic molded article), whereby a web of a web having a width of 1.5 mm and a length of 300 m is obtained. The reel side plate and the backing material are The gap distance between the weight bodies is in the range of about mm1 mm to 〇5 mm, respectively. [Evaluation of the presence or absence of peeling of the adhesive layer] The above-mentioned succeeding material roll is vertically static in a 35 ° C thermostatic chamber. After the state of being placed for 24 hours, the state of the side surface was observed with a microscope. As a result, it was confirmed that the adhesion surface from which the self-rolling body was oozing out was followed by the side plate of the roll. Then, the roll of the material was wound per second. The speed of 丨m was subjected to a full-length 3 (8) extraction test. The result was followed by a failure in the peeling of the substrate. (Example 3) First, a film roll was produced in the same manner as in the example. Easy to ooze out from the side of the heavy body, so A hammer of 5 G g was placed at the subsequent end to apply a winding tension to the entire weight body to 32. 39259, and placed in a state of standing still in the constant temperature bath for 24 hours in the same manner as in Example 1. Thereafter, the microscope was used. The state of the side surface was observed, and it was confirmed that the adhesive oozing from the side surface of the weighted body adhered to the side plate of the roll. Then, the film roll was subjected to a full-length 3 (8) (five) extraction test at a rate of 1 „! per second. The defect of peeling off the layer from the substrate was also not produced. (Example 4) A laminate roll produced in the same manner as in Example 2 was used instead of the film roll produced in the same manner as in Example 1. In the same manner as in Example 3, in the same manner as in Example 3, a weight (4) of the hammer (4) of the backing material was placed in the temperature-sensing tank. Thereafter, the state of (4) was observed under a microscope, and it was confirmed that the subsequent age from the weight-surface bleed was followed by the side plate of the roll, followed by 'the bottom of the roll was carried out at a speed of 1 〇 1 per second. The extraction test, the result of the (four) 丨 layer from the substrate _ bad i times did not occur. (Example 5) Except for the film roll produced in the same manner as in Example 1, the temperature of the strange temperature tank was set to be a thief instead of being set to be hungry, and the same thing as in Example 1 was placed in a pure temperature bath. Money, the state of the side surface was observed by a microscope, and it was confirmed that the adhesive oozing out from the side of the weight body adhered to the side plate of the roll. Next, the slab of the slab was fed at a speed of i m per second for a full-length 3 GGm extraction test, and as a result, the defect of the adhesive layer peeled off from the substrate was not produced once. (Comparative Example 1) A laminate roll was produced in the same manner as in Example i except that the substrate tape was taken up on the core with the substrate facing outward and the adhesive layer was directed toward the roll side (inside) 33 201139259. The tube was placed in a constant temperature in a 35 ° C thermostatic chamber for 24 hours. Thereafter, the state of the side surface was observed by a microscope, and as a result, it was confirmed that the adhesive oozing out from the side surface of the weighted body adhered to the reel. Then, the backing roll was subjected to a pull-out test of a total length of 3 μm at a speed of 1 m per second, and as a result, the adhesive layer was peeled off from the substrate 15 times. (Comparative Example 2) A film roll was produced in the same manner as in Example 2, except that the substrate tape was wound on the core side so that the substrate layer was directed outward (the inner layer). It was left to stand vertically in a constant temperature bath at 35 ° C for 24 hours. Thereafter, the state of the side surface was observed with a microscope, and as a result, it was confirmed that the adhesive oozing from the side surface of the weighted body adhered to the side plate of the roll. Next, this continuous material roll was subjected to a full-length 3 〇〇 melon = extraction test at a rate of 丨m per second, and as a result, the defect of peeling off the adhesive layer from the substrate occurred 17 times. Although this (4) has been read well, the above is not the same as the invention. Anyone who is familiar with the art can make some changes and refinements without departing from the invention. Therefore, the vehicle of the present invention The application is __ defined as the standard. [Simple diagram of the diagram] Figure. Fig. 1 is a perspective view showing an embodiment of the present invention. Fig. 2 is a cross-sectional view showing the internal structure 34 201139259 _____ Γιτ of the bonding material (4) shown in Fig. i. Fig. 3 is a plan view showing the inner side of the side plate of the binder roll of the present invention. Fig. 4 is a cross-sectional view showing an example of an anisotropic conductive tape. Fig. 5 is a cross-sectional view showing an example of a circuit connection in which circuit electrodes are connected to each other. 6(a) to 6(c) are cross-sectional views schematically showing an example of a method of manufacturing a circuit-connected body. 'Picture Figure 8(a) to Fig. 8(c) are cross-sectional views schematically showing other examples of the anisotropic conductive tape. Fig. 9 is a cross-sectional view showing an example of agglomeration generated when the backing member is pulled out from the previous web roll. [Description of Main Element Symbols] 7 is a vertical one showing another embodiment of the binder roll of the present invention: core 2 = side plate 2a: through hole 2b: rib structure portion 5: anisotropic conductive tape (subsequent material tape) 6 ' 26 : substrate 8 ' 18, 28 : adhesive layer 8A · cured product 8a : adhesive composition 35 201139259. 8b : conductive particles 9a, 9b : adhesive layer 10 : secondary material roll 10a : shaft hole 10b : Notch portions 15A, 15B, 15C, 25: Substrate tape 18a: Conductive particle non-containing layer 18b: Conductive particle containing layer 30: First circuit member 31, 41: Circuit substrate 31a, 41a: Main surface 32, 42: Circuit electrode 40: second circuit member 50a: connection portion 100: circuit connection body A, B. front head F1: outer surface F2: inner side surface 36

Claims (1)

201139259 七、申請專利範圍: 1. 一種接著材捲筒,包括: 捲芯; 一對側板’其以相互對向的方式設置於上述捲芯的兩 侧;以及 ,著材帶’其具有帶狀基材及設置於該基材的一面上 的接著劑層’且捲繞於上述捲芯上;並且 上述接著材帶是以上述基材的未形成上述接著劑層的 面朝向上述捲芯側的方式捲繞於上述捲芯上。 2. 如申請專利範圍第1項所述之接著材捲筒,其中上 述接著材帶的長度為2〇〇 m以上。 3. 如申請專利範圍第1項或第2項所述之接著材捲 筒’其中上述接著劑層的於30°C的剪切黏度為100000 Pa.s 以下。 4. 如申請專利範圍第1項至第3項中任一項所述之接 著材捲筒’其申上述接著劑層含有熱自由基硬化型接著劑。 5·如申請專利範圍第4項所述之接著材捲筒,其中上 述熱自由基硬化型接著劑含有1分鐘半衰期溫度為16〇。〇 以下的自由基聚合起始劑。 6.如申請專利範圍第4項或第5項所述之接著材捲 筒’其中上述熱自由基硬化型接著劑含有熱塑性樹脂、包 含於30 C為液狀的自由基聚合性物質的自由基聚合性材 料、及自由基聚合起始劑;並且 相對於上述熱塑性樹脂及上述自由基聚合性材料的總 37 201139259 量100質量份,上述熱自由基硬化型接著劑中的上述自由 基聚合性物質的含量為20質量份〜80質量份。 7. 如申請專利範圍第1項至第3項中任一項所述之接 著材捲筒,其中上述接著劑層含有環氧系接著劑,該環氧 系接著劑包含熱塑性樹脂、包含於3〇它為液狀的環氧樹脂 的熱硬化性材料、及硬化劑;並且 相對於上述熱塑性樹脂及上述熱硬化性材料的總量 1〇〇質量份,上述環氧祕著财的上述環氧樹脂的含量 為20質量份〜8〇質量份。 8. 如中請專利範圍第以至第?項中任 Ϊ材捲筒’其中以上述接著劑層的體積為基準時,上述Ϊ 著劑層的無機填料含量為2〇體積%以下。 9. 如申請專職圍第丨項至帛 ;材捲筒’其中以上述接著劑層的質量為基4= 著劑層的無機填料含量為5〇質量。以下。 10. 如中請糊朗第9賴狀财材 調,於上述接著_中的無機填料為二氧切,並且以該 接者劑層的質量絲準時’上述無機填料的 %以下。 只 11. 如申請專利範圍第9項所述之接著材捲筒,其中 調配於上述接著_中的無機填料為氧她,著 層的質量為基準時,上述無機填料的含4為5Q 下0 U.如申請專利範圍第丨項至第u項中任—項所述之 38 201139259 接著材捲筒,其中上述接著材帶的寬度為0.5 mm〜3.0 mm 〇 13.如申請專利範圍第1項至第12項中任一項所述之 接著材捲筒,其中上述接著材帶是用於電路連接。 39201139259 VII. Patent application scope: 1. A continuous material reel comprising: a core; a pair of side plates ' disposed on opposite sides of the winding core in a mutually opposing manner; and a strip of material having a strip shape a substrate and an adhesive layer disposed on one surface of the substrate and wound around the winding core; and the adhesive tape is oriented toward the core side of a surface of the substrate on which the adhesive layer is not formed The method is wound on the above-mentioned winding core. 2. The binder roll according to claim 1, wherein the length of the above-mentioned backing tape is 2 〇〇 m or more. 3. The binder roll of the above-mentioned adhesive layer according to claim 1 or 2, wherein the above-mentioned adhesive layer has a shear viscosity at 30 ° C of 100000 Pa.s or less. 4. The material roll according to any one of claims 1 to 3, wherein the adhesive layer contains a thermal radical hardening type adhesive. 5. The web roll of claim 4, wherein the thermal radical hardening type adhesive has a one minute half-life temperature of 16 Torr. 〇 The following free radical polymerization initiators. 6. The binder roll according to item 4 or 5, wherein the thermal radical-curable adhesive contains a thermoplastic resin and a radical containing a radical polymerizable substance in a liquid state of 30 C. a polymerizable material and a radical polymerization initiator; and the radical polymerizable substance in the thermal radical-curable adhesive agent in an amount of 100 parts by mass of the total amount of 2011 201129259 of the thermoplastic resin and the radical polymerizable material; The content is 20 parts by mass to 80 parts by mass. The adhesive roll according to any one of claims 1 to 3, wherein the adhesive layer contains an epoxy-based adhesive, and the epoxy-based adhesive contains a thermoplastic resin and is contained in 3 〇 It is a thermosetting material of a liquid epoxy resin and a curing agent; and the epoxy resin is the above-mentioned epoxy with respect to the total amount of the thermoplastic resin and the thermosetting material in an amount of 1 part by mass. The content of the resin is 20 parts by mass to 8 parts by mass. 8. If the scope of the patent is in the first place? In any of the coffin reels, wherein the content of the inorganic filler in the smear layer is 2 vol% or less based on the volume of the above-mentioned adhesive layer. 9. If applying for a full-time sub-item to 帛; the material roll' is based on the mass of the above-mentioned adhesive layer 4 = the inorganic filler content of the agent layer is 5 〇 mass. the following. 10. In the case of the above-mentioned ninth slag, the inorganic filler in the above-mentioned _ is dioxobic, and the mass of the splicer layer is on time 9% or less of the above inorganic filler. 11. The binder roll according to claim 9, wherein the inorganic filler formulated in the above-mentioned _ is oxygen, and the content of the layer is 5Q at the time of the quality of the layer. U. 38 201139259 Subsequent roll according to any one of the claims of the present invention, wherein the width of the above-mentioned adhesive tape is 0.5 mm to 3.0 mm 〇 13. As claimed in the first item The web roll of any one of item 12, wherein the above-mentioned adhesive tape is for electrical connection. 39
TW100108321A 2010-03-12 2011-03-11 Adhesive material reel TWI435841B (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2010056270 2010-03-12
JP2010086330 2010-04-02

Publications (2)

Publication Number Publication Date
TW201139259A true TW201139259A (en) 2011-11-16
TWI435841B TWI435841B (en) 2014-05-01

Family

ID=44563582

Family Applications (1)

Application Number Title Priority Date Filing Date
TW100108321A TWI435841B (en) 2010-03-12 2011-03-11 Adhesive material reel

Country Status (5)

Country Link
JP (3) JPWO2011111784A1 (en)
KR (2) KR20120113803A (en)
CN (2) CN104403589B (en)
TW (1) TWI435841B (en)
WO (1) WO2011111784A1 (en)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6046896B2 (en) * 2012-01-30 2016-12-21 デクセリアルズ株式会社 Film winding body and method for manufacturing film winding body
JP5997306B2 (en) * 2015-02-18 2016-09-28 株式会社ホンマ Corner adhesive tape
KR102615097B1 (en) * 2015-11-25 2023-12-18 가부시끼가이샤 레조낙 Adhesive composition and structure for circuit connection
DE102016200810A1 (en) 2016-01-21 2017-07-27 Tesa Se Dispenser, use of a unwinder, adhesive tape for bonding components and bonding of two components
CN108603078A (en) * 2016-01-29 2018-09-28 日立化成株式会社 Adhesive film and its manufacturing method, bonding agent band and adhesive film spool
CN111466015B (en) * 2018-03-23 2023-08-29 琳得科株式会社 Die bonding film, dicing die bonding sheet, and method for manufacturing semiconductor chip
JP2020073404A (en) * 2019-09-30 2020-05-14 日立化成株式会社 Reel for anisotropic conductive film and anisotropic conductive film roll
JP7446095B2 (en) * 2019-12-03 2024-03-08 デクセリアルズ株式会社 Manufacturing method of film wrapping body and connection body

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3045427B2 (en) * 1992-06-22 2000-05-29 ソニー株式会社 Method and apparatus for attaching anisotropic conductive film
JPH0749504A (en) * 1993-08-06 1995-02-21 Hitachi Electron Eng Co Ltd Slit detector for anisotropically conductive tape
JP3223780B2 (en) * 1996-01-19 2001-10-29 松下電器産業株式会社 Chip mounting equipment
JPH1051115A (en) * 1996-07-29 1998-02-20 Sony Corp Anisotropic conducting film sticking equipment and anisotropic conducting film dividing method
JP4151083B2 (en) * 1997-05-12 2008-09-17 日立化成工業株式会社 Method and apparatus for applying anisotropic conductive adhesive tape
JP3648933B2 (en) * 1997-08-06 2005-05-18 松下電器産業株式会社 Method of attaching anisotropic conductive material
JPH11339575A (en) * 1998-05-22 1999-12-10 Sony Corp Manufacture of anisotropic conductive tape and its manufacturing device
JP3680669B2 (en) * 1999-12-17 2005-08-10 ソニーケミカル株式会社 Multilayer anisotropic conductive film laminate
JP4648521B2 (en) * 2000-07-17 2011-03-09 スタンレー電気株式会社 Manufacturing method of liquid crystal device
JP2002226822A (en) * 2001-01-30 2002-08-14 Three M Innovative Properties Co Method of adhering substrates by using photo activating type adhesive film
JP2004323621A (en) * 2003-04-23 2004-11-18 Hitachi Chem Co Ltd Adhesive material tape
JP4654566B2 (en) * 2003-04-23 2011-03-23 日立化成工業株式会社 Adhesive tape connection method and adhesive tape connector
JP4239585B2 (en) * 2002-12-24 2009-03-18 日立化成工業株式会社 Adhesive tape connection method and adhesive tape connector
JP4333140B2 (en) * 2003-01-08 2009-09-16 日立化成工業株式会社 Method for producing adhesive tape
CN100548840C (en) * 2002-07-30 2009-10-14 日立化成工业株式会社 The method of attachment of adhesive material tape connector and adhesive material tape
JP3991268B2 (en) * 2002-11-29 2007-10-17 日立化成工業株式会社 Film adhesive for connecting circuit members and semiconductor device using the same
EP1754762A4 (en) * 2004-06-09 2009-07-22 Hitachi Chemical Co Ltd Adhesive composition, circuit connecting material, connecting structure for circuit member, and semiconductor device
JP4595459B2 (en) * 2004-09-15 2010-12-08 カシオ計算機株式会社 Adhesive adhesive transfer method
JP2009004354A (en) * 2007-05-23 2009-01-08 Hitachi Chem Co Ltd Adhesive reel and method of manufacturing circuit connector using the same
JP5456475B2 (en) * 2007-09-05 2014-03-26 日立化成株式会社 Adhesive and connection structure using the same
JP5332259B2 (en) * 2008-03-28 2013-11-06 デクセリアルズ株式会社 Anisotropic conductive film transfer tool and connection method

Also Published As

Publication number Publication date
JPWO2011111784A1 (en) 2013-06-27
WO2011111784A1 (en) 2011-09-15
JP2014037544A (en) 2014-02-27
CN102712834A (en) 2012-10-03
CN102712834B (en) 2014-11-26
TWI435841B (en) 2014-05-01
CN104403589B (en) 2017-01-11
JP2015083691A (en) 2015-04-30
KR20120113803A (en) 2012-10-15
KR20140054438A (en) 2014-05-08
KR101763458B1 (en) 2017-07-31
CN104403589A (en) 2015-03-11
JP5928567B2 (en) 2016-06-01

Similar Documents

Publication Publication Date Title
TW201139259A (en) Adhesive material reel
WO2013024544A1 (en) Adhesive material reel
JP4993880B2 (en) Anisotropic conductive adhesive sheet and finely connected structure
TWI328602B (en)
TW201108876A (en) Circuit connecting material, connection structure for circuit member using the same and production method thereof
TW201216301A (en) Anisotropic conductive film
JP2011192651A (en) Anisotropic conductive film, connection method, and connection structure
JP2014102943A (en) Anisotropic conductive film, connection method and joined body
JP2005200521A (en) Adhesive film and method of manufacturing adhesive film
US20230287246A1 (en) Method for manufacturing joined body, joined body, and hot-melt adhesive sheet
TWI334880B (en) Circuit connecting adhesive with anisotropic conductivity connecting method of circuit board and circuit connecting construction by using the adhesive
TWI450942B (en) Then the material tape and then the material tape wound body
JP7020029B2 (en) Conductive adhesive film
TW201640631A (en) COF semiconductor package, and liquid crystal device
JP4994653B2 (en) Anisotropic conductive adhesive sheet
JP6408759B2 (en) Adhesive composition and film winding body
JP2008133411A (en) Adhesive film for electrical connection
JPH1021740A (en) Anisotropic conductive composition and film
JP7446095B2 (en) Manufacturing method of film wrapping body and connection body
JP2005197032A (en) Anisotropic conductive film
JP7294145B2 (en) Adhesive composition, connection structure and method for producing the same
JP2007018760A (en) Anisotropic conduction film for glass base plate connection
TW201242884A (en) Circuit connecting tape, adhesive reel and method for manufacturing circuit-connected body
CN115349003B (en) Adhesive composition, adhesive film, connection structure, and method for producing same
JP5370694B2 (en) Connection structure