JP4437505B2 - Laminated tape for packaging materials - Google Patents
Laminated tape for packaging materials Download PDFInfo
- Publication number
- JP4437505B2 JP4437505B2 JP2008225174A JP2008225174A JP4437505B2 JP 4437505 B2 JP4437505 B2 JP 4437505B2 JP 2008225174 A JP2008225174 A JP 2008225174A JP 2008225174 A JP2008225174 A JP 2008225174A JP 4437505 B2 JP4437505 B2 JP 4437505B2
- Authority
- JP
- Japan
- Prior art keywords
- weight
- paper
- parts
- antistatic agent
- adhesive layer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
- C09J7/35—Heat-activated
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
- C08L71/02—Polyalkylene oxides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0075—Antistatics
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/08—Copolymers of ethene
- C08L23/0807—Copolymers of ethene with unsaturated hydrocarbons only containing more than three carbon atoms
- C08L23/0815—Copolymers of ethene with aliphatic 1-olefins
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
- C09J11/08—Macromolecular additives
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J123/00—Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J123/00—Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers
- C09J123/02—Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers not modified by chemical after-treatment
- C09J123/04—Homopolymers or copolymers of ethene
- C09J123/08—Copolymers of ethene
- C09J123/0846—Copolymers of ethene with unsaturated hydrocarbons containing other atoms than carbon or hydrogen atoms
- C09J123/0853—Vinylacetate
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/20—Adhesives in the form of films or foils characterised by their carriers
- C09J7/22—Plastics; Metallised plastics
- C09J7/24—Plastics; Metallised plastics based on macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- C09J7/241—Polyolefin, e.g.rubber
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/20—Adhesives in the form of films or foils characterised by their carriers
- C09J7/29—Laminated material
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2203/00—Applications of adhesives in processes or use of adhesives in the form of films or foils
- C09J2203/326—Applications 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
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2301/00—Additional features of adhesives in the form of films or foils
- C09J2301/10—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet
- C09J2301/16—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the structure of the carrier layer
- C09J2301/162—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the structure of the carrier layer the carrier being a laminate constituted by plastic layers only
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2301/00—Additional features of adhesives in the form of films or foils
- C09J2301/30—Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier
- C09J2301/304—Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier the adhesive being heat-activatable, i.e. not tacky at temperatures inferior to 30°C
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2423/00—Presence of polyolefin
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2423/00—Presence of polyolefin
- C09J2423/04—Presence of homo or copolymers of ethene
- C09J2423/046—Presence of homo or copolymers of ethene in the substrate
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2467/00—Presence of polyester
- C09J2467/006—Presence of polyester in the substrate
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2471/00—Presence of polyether
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Adhesive Tapes (AREA)
- Wrappers (AREA)
- Laminated Bodies (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Packages (AREA)
Description
本発明は、チップ型電子部品の搬送時などに該電子部品等を包装する包装材用として使用される積層テープに関するものである。 The present invention relates to a laminated tape used as a packaging material for wrapping electronic components and the like when conveying chip-type electronic components.
チップ部品を搬送する方法として、該電子部品を包装材に包装して搬送する、テーピングリール方式が知られている。このテーピングリール方式では、テープ状厚紙の長さ方向に一定間隔でチップ型部品収納用のポケットを設けたキャリア(紙製包装基材)に部品を挿入し、上からカバーテープ(トップテープ)を熱シールして封入して、リール状に巻き取られ搬送される。搬送後には、回路基板などの作製工程において、カバーテープを剥離し、チップ部品をエアー吸着ノズルで吸着して、基板上に実装するシステムが主流となっている As a method of transporting chip components, a taping reel method is known in which the electronic components are packaged and transported in a packaging material. In this taping reel method, parts are inserted into a carrier (paper packaging substrate) with pockets for storing chip-type parts at regular intervals along the length of the tape-shaped cardboard, and cover tape (top tape) is applied from above. It is heat-sealed and sealed, wound up in a reel shape, and conveyed. After transport, in the manufacturing process of circuit boards and the like, the system that peels the cover tape and sucks the chip parts with the air suction nozzle and mounts on the board has become the mainstream
このようなテーピングから基盤へのチップ供給までの一連の工程において、電子部品の包装材として用いられるカバーテープに対しては、チップを確実に供給するために次のような性能が要求されている。すなわち、(1)紙製包装基材に対して良好な接着性を有すること。(2)カバーテープ剥離の際、安定な剥離性があり、紙製包装基材からの毛羽発生などなく、部品実装時のトラブルがないこと。(3)カバーテープ剥離時に発生する剥離帯電によりチップがポケットから飛び出すのを抑制する、いわゆる帯電防止性に優れること。(4)輸送途中、環境条件に起因して部品がカバーテープに付着しないことなどである。 In such a series of steps from taping to chip supply to the substrate, the following performance is required for the cover tape used as a packaging material for electronic components in order to supply chips reliably. . That is, (1) having good adhesion to a paper packaging substrate. (2) When the cover tape is peeled off, there should be stable peelability, no fluff is generated from the paper packaging substrate, and there is no trouble when mounting the components. (3) It is excellent in so-called antistatic property that suppresses the chip from popping out of the pocket due to peeling electrification generated when the cover tape is peeled off. (4) During transportation, parts do not adhere to the cover tape due to environmental conditions.
特に近年、チップ型電子部品においては部品サイズが益々小型化し、カバーテープを剥離する際に生じる紙製包装基材表層を剥がし取る現象(毛羽発生)などが、実装機の吸着ノズルへの悪影響を与え、実装率の低下をもたらすなどの問題が発生している。このため、特に極小部品の包装等に用いられるカバーテープにおいては、良好な剥離性を有し、剥離時、紙製包装基材の表面を毛羽立たせないことが、帯電防止性能とともに重要な性能であり、このようなカバーテープが所望されている。 Particularly in recent years, chip-type electronic components have become increasingly smaller in size, and the phenomenon of flaking off the surface of the paper packaging substrate that occurs when the cover tape is peeled off (occurrence of fluff) has an adverse effect on the suction nozzle of the mounting machine. Giving rise to a decrease in the mounting rate. For this reason, especially in cover tapes used for packaging of extremely small parts, it has an excellent releasability, and it is an important performance along with antistatic performance that the surface of the paper packaging substrate is not fluffed at the time of peeling. There is a desire for such a cover tape.
包装材の剥離帯電圧を抑制する方法としては、ポリ酢酸ビニル系樹脂、エチレン系共重合体、アクリル系樹脂及びワックス類から選択された少なくとも1種の成分を表面又は内部に含有する包装基材と、分子内にカルボキシル基又はアシルオキシ基を含有するオレフィン系共重合体、アイオノマー樹脂、及び芳香族ビニル化合物と共役ジエン系化合物とのブロック共重合体から選択された少なくとも1種の重合体を含む樹脂組成物により形成された接着樹脂層を有しているカバーテープを組み合わせる方法が提案されている(特許文献1参照)。この方法では、種類の違う基材とカバーテープを組み合わせた場合効果が得られなくなるため、組み合わせる基材の種類を問わず帯電防止性能を発揮することができるカバーテープが所望されている。 Packaging substrate containing at least one component selected from polyvinyl acetate resin, ethylene copolymer, acrylic resin and wax on the surface or inside as a method for suppressing the peeling voltage of the packaging material And an olefin copolymer containing a carboxyl group or an acyloxy group in the molecule, an ionomer resin, and at least one polymer selected from a block copolymer of an aromatic vinyl compound and a conjugated diene compound. A method of combining a cover tape having an adhesive resin layer formed of a resin composition has been proposed (see Patent Document 1). In this method, since an effect cannot be obtained when different types of base materials and cover tapes are combined, a cover tape that can exhibit antistatic performance regardless of the types of base materials to be combined is desired.
又、帯電防止性を有するカバーテープとしては、ポリオレフィン系樹脂に帯電防止剤(界面活性剤=低分子型帯電防止剤)を練りこんだ接着剤層が中間層を介して支持基材上に積層されたものが知られている(特許文献2参照)。このカバーテープは、帯電防止剤とし配合した低分子型帯電防止剤が、カバーテープと紙製包装基材の界面にブリードし、ピール強度を低下させてしまう。このため、接着性を確保する為に接着付与剤を配合し、ピール強度を維持している。しかしながら、低分子成分である帯電防止剤は、接着層内を移動するため、時として紙製包装基材との接着力が高くなる場合や、局部的に接着力が上昇してしまうなどして、カバーテープを剥がす際、紙製包装基材の表層を引きちぎるなどして毛羽を発生させてしまう場合があった。このようなカバーフィルムは、部品のサイズ等によっては十分実用に耐え得るものであるが、極小サイズのチップ型電子部品においては、カバーテープを剥離する際に生じる紙製包装基材表層を剥がしとる現象(毛羽発生)などが、実装機の吸着ノズルへの悪影響を与え、実装率の低下をもたらす等の問題が発生している。このため、特に極小部品の包装等に用いられるカバーテープにとっては、良好な剥離性を有し、剥離時、紙製包装基材の表面を毛羽立たせないことが帯電防止性能とともに重要な性能である。 In addition, as an antistatic cover tape, an adhesive layer in which an antistatic agent (surfactant = low molecular weight antistatic agent) is kneaded into a polyolefin resin is laminated on a supporting substrate via an intermediate layer. Is known (see Patent Document 2). In this cover tape, the low molecular weight antistatic agent blended as the antistatic agent bleeds at the interface between the cover tape and the paper packaging substrate, and the peel strength is lowered. For this reason, in order to ensure adhesiveness, the adhesion imparting agent is mix | blended and the peel strength is maintained. However, since the antistatic agent, which is a low molecular component, moves in the adhesive layer, sometimes the adhesive force with the paper packaging substrate is increased, or the adhesive force is locally increased. When the cover tape is peeled off, the surface layer of the paper packaging substrate may be torn off to generate fluff. Such a cover film can be sufficiently practically used depending on the size of the component, but in the case of a very small size chip-type electronic component, the surface layer of the paper packaging substrate that is generated when the cover tape is peeled off is peeled off. The phenomenon (generation of fluff) has an adverse effect on the suction nozzle of the mounting machine, causing problems such as a decrease in mounting rate. For this reason, especially for cover tapes used for packaging of extremely small parts, it has an excellent releasability, and at the time of peeling, it is important performance along with antistatic performance not to fluff the surface of the paper packaging substrate. .
また、接着剤層の表面抵抗率が温度湿度に依存して変化し、これにより接着剤層表面が帯電することを防ぐ方法として、接着剤に高分子型帯電防止剤を配合することが検討されている(特許文献3参照)。このようなカバーテープでは、キャリア台紙との接着性を確保するために、接着剤中に多量の粘着付与剤を配合するために接着力が適性な値よりも強くなったり、経時的に剥離性が低下し、紙製包装基材表面の紙繊維を引き剥がし(毛羽発生)、実装での不良を引き起こす場合があり、このような問題のないカバーテープが望まれている。 In addition, as a method for preventing the surface resistivity of the adhesive layer from changing depending on temperature and humidity, and thereby causing the surface of the adhesive layer to be charged, it has been studied to add a polymer type antistatic agent to the adhesive. (See Patent Document 3). In such a cover tape, in order to ensure adhesion with the carrier mount, a large amount of tackifier is added to the adhesive, so that the adhesive strength becomes stronger than an appropriate value, or the releasability with time. The paper tape on the surface of the paper packaging substrate is peeled off (fluff generation), which may cause defects in mounting, and a cover tape that does not have such a problem is desired.
さらにまた、カバーテープを紙製包装基材から剥離する際に生じる剥離振動(ビビリ)により、キャリア台紙キャビティ内のチップ部品が傾いたりキャビティから飛び出す現象(チップ飛び)などが発生し、チップ部品をエアー吸着ノズルで吸着する際正確な位置での吸着ができず、実装率低下の原因となっている。このような剥離振動の問題は、チップ部品の小型化軽量化が進むにつれますます顕著となっている。しかも、同一のカバーテープを用いても、キャリア台紙の種類やロットにより接着強度が異なるため、一定の剥離力によりカバーテープを剥離させ、剥離振動を低減させるためには、テーピング機での圧着条件を紙製包装基材の種類やロットがかわるごとに調整するなど、高レベルな管理が要求される。このため、キャリア台紙の種類やロットによらず、一定の圧着条件により一定の接着力を安定して発現し、剥離振動を生じにくいカバーテープが望まれている。
本発明の目的は、キャリアテープ等の包装基材に対する熱接着性に優れるとともに、帯電防止性能と、剥離時に紙製包装基材の表面を毛羽立たせることなく剥離できる良好な剥離性を長期間にわたり維持し、高い実装率を確保できる包装材用積層テープを提供することにある。
本発明の他の目的は、湿度等環境が変化しても適度な接着力を安定して維持し、キャリア台紙の種類やロットに依らずに一定の圧着条件により一定の接着力を安定して発現し、極小チップ部品の包装に使用した場合であっても、高い実装率を確保できる包装材用積層テープを提供することにある。
The object of the present invention is excellent in thermal adhesiveness to a packaging substrate such as a carrier tape, antistatic performance, and good releasability capable of peeling without fluffing the surface of the paper packaging substrate during peeling over a long period of time. An object of the present invention is to provide a laminated tape for packaging material that can maintain and ensure a high mounting rate.
Another object of the present invention is to stably maintain an appropriate adhesive force even when the environment such as humidity changes, and to maintain a constant adhesive force by a constant pressure condition irrespective of the type and lot of the carrier mount. Even if it is a case where it expresses and it is a case where it uses for the packaging of a microchip component, it is providing the laminated tape for packaging materials which can ensure a high mounting rate.
上記目的を達成するため鋭意検討した結果、支持基材層上に設ける熱接着剤層を特定の成分で構成すると、包装基材に対する接着性、帯電防止性、剥離時の毛羽発生抑制、剥離振動の抑制の何れをも充足できることを見出し、本発明を完成した。 As a result of diligent studies to achieve the above object, when the thermal adhesive layer provided on the support substrate layer is composed of specific components, adhesion to the packaging substrate, antistatic properties, suppression of fluff generation during peeling, peeling vibration It was found that any of the suppressions can be satisfied, and the present invention has been completed.
すなわち、本発明は、支持基材層上に、ポリオレフィン系樹脂を主成分とするベースポリマー、粘着付与樹脂としての脂環族石油樹脂、高分子型帯電防止剤を含む熱接着剤層が積層されている包装材用積層テープであって、前記ベースポリマーがエチレン−α−オレフィン共重合体を5〜40重量%含むとともに、熱接着剤層が、ベースポリマー100重量部に対して、粘着付与樹脂としての脂環族石油樹脂を1〜20重量部、ポリエーテル構造を含む高分子型帯電防止剤を1〜30重量部含むことを特徴とする包装材用積層テープを提供する。 That is, in the present invention, a thermal adhesive layer containing a base polymer composed mainly of a polyolefin resin , an alicyclic petroleum resin as a tackifying resin , and a polymer-type antistatic agent is laminated on a supporting base material layer. A laminated tape for packaging material, wherein the base polymer contains 5 to 40% by weight of an ethylene-α-olefin copolymer, and the thermal adhesive layer is a tackifying resin with respect to 100 parts by weight of the base polymer. 1-20 parts by weight of an alicyclic petroleum resin as to provide a packaging material for a laminated tape according to claim 1 to 30 parts by weight including that of the polymeric antistatic agent containing a polyether structure.
上記包装材用積層テープにおいて、該包装材用積層テープは、チップ型電子部品を搬送する際の包装材用積層テープとして使用できる。 In the packaging tape, the packaging tape can be used as a packaging tape when a chip-type electronic component is conveyed.
なお、本明細書では下記の発明についても説明する。 In this specification, the following invention is also described.
支持基材層上に、ポリオレフィン系樹脂を主成分とするベースポリマー、粘着付与樹脂、高分子型帯電防止剤を含む熱接着剤層が積層されている包装材用積層テープであって、熱接着剤層が、ベースポリマー100重量部に対して、粘着付与樹脂を1〜20重量部、高分子型帯電防止剤を1〜30重量部含むことを特徴とする包装材用積層テープ。 A laminated tape for packaging materials in which a thermal adhesive layer containing a base polymer composed mainly of a polyolefin resin, a tackifying resin, and a polymer type antistatic agent is laminated on a supporting base material layer, The laminated tape for packaging materials, wherein the agent layer contains 1 to 20 parts by weight of a tackifier resin and 1 to 30 parts by weight of a polymer-type antistatic agent with respect to 100 parts by weight of the base polymer.
上記高分子型帯電防止剤としては、ポリエーテル構造を含むものを好適に使用することができる。 As the polymer type antistatic agent, those containing a polyether structure can be suitably used.
熱接着剤層は、ベースポリマー100重量部に対して、粘着付与樹脂を2〜13重量部、高分子型帯電防止剤を10〜30重量部含むのが好ましい。 The thermal adhesive layer preferably contains 2 to 13 parts by weight of a tackifier resin and 10 to 30 parts by weight of a polymer antistatic agent with respect to 100 parts by weight of the base polymer.
熱接着剤層を構成するベースポリマーには、エチレン−α−オレフィン共重合体を少なくとも含み、その含有量はベースポリマーの50重量%以下であることが好ましい。 The base polymer constituting the thermal adhesive layer contains at least an ethylene-α-olefin copolymer, and the content thereof is preferably 50% by weight or less of the base polymer.
ポリエーテル構造を含む高分子型帯電防止剤としては、ポリエーテルエステルアミドを含む高分子型帯電防止剤を好適に使用できる。 As the polymer antistatic agent containing a polyether structure, a polymer antistatic agent containing a polyether ester amide can be suitably used.
熱接着剤層の厚みは、5〜50μmであり、熱接着剤層の表面抵抗率は1013Ω/□以下であるのが好ましい。また、本発明の包装材用積層テープを2種類の異なる紙製包装基材に190℃で熱シールした際に、各々の紙製包装基材に対する該テープの接着力の差が2倍以内であるのが好ましい。 The thickness of the thermal adhesive layer is 5 to 50 μm, and the surface resistivity of the thermal adhesive layer is preferably 10 13 Ω / □ or less. In addition, when the laminated tape for packaging material of the present invention is heat-sealed to two different paper packaging substrates at 190 ° C., the difference in adhesive strength of the tape to each paper packaging substrate is less than twice. Preferably there is.
包装材用積層テープを紙製基材に熱シールした後、紙製包装基材から剥離させた際の接着剤層に生じる剥離帯電圧(23℃×65%RH、剥離角度180°、剥離速度5000mm/分、電極と接着剤層との距離5mm)の絶対値が200V以下であることが好ましい。 Peeling voltage (23 ° C x 65% RH, peel angle 180 °, peel speed) generated in the adhesive layer when the packaging tape is heat-sealed to the paper base material and then peeled from the paper base material The absolute value of 5000 mm / min and the distance between the electrode and the adhesive layer of 5 mm is preferably 200 V or less.
熱接着剤層を構成する接着剤組成物は、該接着剤組成物を35℃×80%RHの条件にした高温恒湿機中に24時間保存した際の水分率が0.5%以下であるのが好ましい。 The adhesive composition constituting the thermal adhesive layer has a moisture content of 0.5% or less when the adhesive composition is stored for 24 hours in a high-temperature humidity chamber under conditions of 35 ° C. × 80% RH. Preferably there is.
本発明の包装材用積層テープは、紙製包装基材に熱シールした後、紙製包装基材表層の紙繊維を毛羽立たせることなしに剥離できることが好ましい。 It is preferable that the laminated tape for packaging material of the present invention can be peeled without fuzzing the paper fibers on the surface of the paper packaging substrate after heat sealing to the paper packaging substrate.
本発明の包装材用積層テープは、熱接着剤層が特定の成分により構成されているので、キャリアテープなどの包装基材に対する熱接着性に優れるとともに、帯電防止性能と良好な剥離性を長期にわたり維持できる。このため、本発明の包装材用積層テープを小型電子部品包装材のトップカバーとして使用した場合には、剥離時の紙製包装基材表層の毛羽立ちを大幅に抑制することができ、毛羽立ちによる実装機のエアーノズルへの影響も抑制することができる。また、組み合わせる基材の種類を問わず、トップカバー表面の帯電を防止し、帯電による電子部品への影響なども抑制するため、良好な部品実装性が可能となる。さらにまた、一般に普及している紙製包装基材に対して、基材の種類に依らず一定の圧着条件により一定の接着性を安定して発現する。このため、包装材用積層テープを紙製包装基材に熱シールする際に、紙製包装基材の種類やロットに応じて圧着条件を細かく調整することを要せず、剥離時には一定の力により良好に剥離できるため、剥離振動が抑制される。これらの接着性、剥離性、帯電防止性、剥離振動防止性などの性能は、テーピングにより電子部品等を包装後、長期間倉庫等で保管した後でも劣化することなく、高い実装率を達成できる。特に、静電気が発生しやすい乾燥した環境でも優れた帯電防止性能を発揮し、熱接着層を吸水後の水分率が一定の値以下である接着剤組成物により構成すれば、高湿度下や結露時においても一定の接着力を発現し、該一定の接着力を長期間にわたり維持するため、湿度等に左右されず安定した実装が可能となる。 In the laminated tape for packaging material of the present invention, the thermal adhesive layer is composed of a specific component, so that it has excellent thermal adhesion to a packaging substrate such as a carrier tape, and has long-term antistatic performance and good peelability. Can be maintained over time. For this reason, when the laminated tape for packaging material of the present invention is used as the top cover of a small electronic component packaging material, fluffing on the surface layer of the paper packaging substrate during peeling can be greatly suppressed, and mounting due to fluffing The influence on the air nozzle of the machine can also be suppressed. In addition, regardless of the type of base material to be combined, charging of the top cover surface is prevented, and the influence of the charging on the electronic component is also suppressed, so that favorable component mountability is possible. Furthermore, with respect to a paper packaging substrate that has been widely used, a certain level of adhesiveness is stably exhibited under certain pressure bonding conditions regardless of the type of the substrate. For this reason, when heat-sealing the laminated tape for packaging material to the paper packaging substrate, it is not necessary to finely adjust the crimping conditions according to the type and lot of the paper packaging substrate, and a constant force at the time of peeling. Therefore, peeling vibration is suppressed. Performance such as adhesiveness, peelability, antistatic property, peel vibration prevention property can be achieved without deterioration even after electronic parts are packaged by taping and stored in a warehouse for a long time. . In particular, if anti-static performance is exhibited even in a dry environment where static electricity is likely to be generated, and the thermal adhesive layer is made of an adhesive composition that has a moisture content of a certain value or less after water absorption, it is highly humid or dew condensation. Even at times, a constant adhesive force is expressed and the constant adhesive force is maintained for a long period of time, so that stable mounting is possible regardless of humidity.
本発明の包装材用積層テープは、支持基材層と支持基材層上に設けられた熱接着剤層とで構成されている。支持基材層を構成する支持基材としては、自己支持性を有するものであればよく、例えば和紙、薄葉紙、クレープ紙、混抄紙、複合紙などの紙類;不織布、布;ポリエチレン、ポリプロピレン、エチレン−酸共重合樹脂などのオレフィン系樹脂、ポリプロピレン変性樹脂、スチレン系熱可塑性エラストマーなどの熱可塑性エラストマー、ポリエチレンテレフタレート、ポリブチレンテレフタレート、ポリエチレンナフタレートなどのポリエステル等の熱可塑性樹脂で構成されたプラスチックフィルム又はシート;銅、アルミニウムなどの金属で構成された金属箔又は薄板;これらの積層体などが挙げられる。 The laminated tape for packaging material of the present invention is composed of a supporting base layer and a thermal adhesive layer provided on the supporting base layer. The supporting substrate constituting the supporting substrate layer may be any material having self-supporting properties, for example, paper such as Japanese paper, thin paper, crepe paper, mixed paper, composite paper; non-woven fabric, cloth; polyethylene, polypropylene, Plastics made of thermoplastic resins such as olefin resins such as ethylene-acid copolymer resins, polypropylene modified resins, thermoplastic elastomers such as styrene thermoplastic elastomers, and polyesters such as polyethylene terephthalate, polybutylene terephthalate, and polyethylene naphthalate. Films or sheets; metal foils or thin plates composed of metals such as copper and aluminum; and laminates thereof.
前記支持基材は、融点が90℃以上であるのが好ましい。融点が90℃未満の場合には、金属製アイロンなどを用いて熱圧着によりテーピングを行う際に、支持基材が溶融してアイロンなどに付着し、本来の包装という目的を達成できなくなる恐れがある。 The supporting substrate preferably has a melting point of 90 ° C. or higher. If the melting point is less than 90 ° C, when taping is performed by thermocompression bonding using a metal iron or the like, the support base material may melt and adhere to the iron or the like, and the original packaging purpose may not be achieved. is there.
支持基材層の表面(接着剤層とは反対の面)は、慣用の表面処理、易滑処理、帯電防止処理などが施されていてもよい。また、支持基材層の接着剤層と接する面には、オゾン処理、コロナ処理などの投錨性を向上するための処理が施されていてもよく、特に支持基材がプラスチックフィルムの場合は、アンカーコート剤塗布による投錨性向上手段が採られていてもよい。 The surface of the support substrate layer (the surface opposite to the adhesive layer) may be subjected to conventional surface treatment, easy slip treatment, antistatic treatment, and the like. In addition, the surface of the supporting base material layer that is in contact with the adhesive layer may be subjected to treatment for improving anchoring properties such as ozone treatment and corona treatment, particularly when the supporting base material is a plastic film. Anchoring property improving means by applying an anchor coating agent may be employed.
支持基材層の厚みは、機械的強度、ハンドリング性などが損なわれない範囲で用途に応じて広い範囲で選択できるが、一般には5〜100μm程度、好ましくは10〜50μm程度である。 The thickness of the supporting base material layer can be selected in a wide range depending on the application within the range in which the mechanical strength, handling property and the like are not impaired, but is generally about 5 to 100 μm, preferably about 10 to 50 μm.
熱接着剤層は、ベースポリマー、粘着付与樹脂、及び高分子型帯電防止剤を含む熱可塑性接着剤で構成されている。ベースポリマーは、ポリオレフィン系樹脂を主成分とし、必要に応じてその他のポリマー、例えば酢酸ビニル系樹脂などの熱可塑性樹脂、熱可塑性エラストマーなどを組み合わせて使用できる。なお、ベースポリマーはポリオレフィン系樹脂のみで構成されていてもよく、1種又は2種以上を組み合わせて使用できる。 The thermal adhesive layer is composed of a thermoplastic adhesive containing a base polymer, a tackifying resin, and a polymer type antistatic agent. The base polymer is mainly composed of a polyolefin-based resin, and other polymers, for example, a thermoplastic resin such as a vinyl acetate-based resin, a thermoplastic elastomer, or the like can be used in combination. In addition, the base polymer may be comprised only with polyolefin resin, and can be used 1 type or in combination of 2 or more types.
ポリオレフィン系樹脂としては、例えば、ポリエチレン(低密度ポリエチレン、線状低密度ポリエチレン、メタロセン触媒法ポリエチレン、高密度ポリエチレンなど)、ポリプロピレン、エチレン−α−オレフィン共重合体などのポリオレフィン;エチレン共重合体(例えば、エチレン−アクリル酸共重合体(EAA)、エチレン−メタクリル酸共重合体(EMAA)などのエチレン−不飽和カルボン酸共重合体;アイオノマー;エチレン−アクリル酸メチル共重合体、エチレン−アクリル酸エチル共重合体(EEA)、エチレン−メタクリル酸メチル共重合体などのエチレン−(メタ)アクリル酸エステル共重合体;エチレン−酢酸ビニル共重合体(EVA)、エチレン−ビニルアルコール共重合体など);ポリプロピレン変性樹脂などが挙げられる。ポリオレフィン系樹脂は、ベースポリマー中に60重量%以上、好ましくは80重量%以上、特に好ましくは95重量%以上含まれる。 Examples of the polyolefin resin include polyolefins such as polyethylene (low density polyethylene, linear low density polyethylene, metallocene catalyzed polyethylene, high density polyethylene, etc.), polypropylene, ethylene-α-olefin copolymer; ethylene copolymer ( For example, ethylene-unsaturated carboxylic acid copolymer such as ethylene-acrylic acid copolymer (EAA) and ethylene-methacrylic acid copolymer (EMAA); ionomer; ethylene-methyl acrylate copolymer, ethylene-acrylic acid (Ethylene copolymer (EEA), ethylene- (meth) acrylic acid ester copolymer such as ethylene-methyl methacrylate copolymer; ethylene-vinyl acetate copolymer (EVA), ethylene-vinyl alcohol copolymer, etc.)) ; Polypropylene modified resin, etc. It is below. The polyolefin resin is contained in the base polymer in an amount of 60% by weight or more, preferably 80% by weight or more, particularly preferably 95% by weight or more.
その他のポリマーとしての酢酸ビニル系樹脂としては、例えば、ポリ酢酸ビニル、酢酸ビニル−(メタ)アクリル酸エステル共重合体、酢酸ビニル−ビニルエステル共重合体、酢酸ビニル−マレイン酸エステル共重合体などが挙げられる。 Examples of vinyl acetate resins as other polymers include polyvinyl acetate, vinyl acetate- (meth) acrylic acid ester copolymers, vinyl acetate-vinyl ester copolymers, vinyl acetate-maleic acid ester copolymers, and the like. Is mentioned.
熱可塑性エラストマーとしては例えば、SIS(スチレン−イソプレン−スチレンブロック共重合体)、SBS(スチレン−ブタジエン−スチレンブロック共重合体)、SEBS(スチレン−エチレン−ブチレン−スチレンブロック共重合体)、SEPS(スチレン−エチレン−プロピレン−スチレンブロック共重合体)、SEP(スチレン−エチレン−プロピレンブロック共重合体)などのスチレン系熱可塑性エラストマー;スチレン系ブロックコポリマー(例えばスチレン含有量5重量%以上のスチレン系ブロックコポリマー);ポリウレタン系熱可塑性エラストマー;ポリエステル系熱可塑性エラストマー;ポリプロピレンとEPT(三元系エチレン−プロピレンゴム)とのポリマーブレンドなどのブレンド系熱可塑性エラストマーなどが挙げられる。 Examples of the thermoplastic elastomer include SIS (styrene-isoprene-styrene block copolymer), SBS (styrene-butadiene-styrene block copolymer), SEBS (styrene-ethylene-butylene-styrene block copolymer), SEPS ( Styrenic thermoplastic elastomers such as styrene-ethylene-propylene-styrene block copolymer) and SEP (styrene-ethylene-propylene block copolymer); styrene block copolymer (for example, styrene block having a styrene content of 5% by weight or more) Copolymer); polyurethane-based thermoplastic elastomer; polyester-based thermoplastic elastomer; blend-based thermoplastic elastomer such as polymer blend of polypropylene and EPT (ternary ethylene-propylene rubber) And the like.
ベースポリマーは、エチレン−α−オレフィン共重合体をベースポリマー中50重量%以下の範囲内で含んでいることが好ましい。すなわち、ベースポリマーはエチレン−α−オレフィン共重合体と、エチレン−α−オレフィン共重合体以外のポリオレフィン系樹脂と、必要に応じてその他のポリマーとの組み合わせにより構成されているのが好ましい。エチレン−α−オレフィン共重合体の含有量は、より好ましくはベースポリマーの5〜40重量%であり、特に好ましくは10〜35重量%である。ベースポリマー中にエチレン−α−オレフィン共重合体を含むことにより、接着剤は適度な接着力と良好な剥離性を発現し、さらに粘着特性の経時的な変化を防止できる。エチレン−α−オレフィン共重合体の含有量が50重量%より多いと、接着力が適正な範囲である10〜70gf(98.1〜687mN)を超えてしまい、剥離後、紙製包装基材に毛羽が発生したり、熱接着剤層が柔らかくなりすぎ、テーピング機での圧着時に接着剤がシールコテなどに付着する等のトラブルが発生し、好ましくない。エチレン−α−オレフィン共重合体をベースポリマー中に含む場合は例えば、その他のポリマーとして、酢酸ビニル含有量15重量%以下であるエチレン−酢酸ビニル共重合体樹脂又は、前記酢酸ビニル含有量15重量%以下であるエチレン−酢酸ビニル共重合体樹脂に加えて低密度ポリエチレンを使用するのが好ましい。この際の好ましい配合量は例えば、低密度ポリエチレン:0〜10重量%、酢酸ビニル含有量15重量%以下であるエチレン−酢酸ビニル共重合体樹脂:50〜95重量%、エチレン−α−オレフィン共重合体:5〜40重量%である。 The base polymer preferably contains an ethylene-α-olefin copolymer within the range of 50% by weight or less in the base polymer. That is, the base polymer is preferably composed of a combination of an ethylene-α-olefin copolymer, a polyolefin resin other than the ethylene-α-olefin copolymer, and, if necessary, other polymers. The content of the ethylene-α-olefin copolymer is more preferably 5 to 40% by weight of the base polymer, and particularly preferably 10 to 35% by weight. By including the ethylene-α-olefin copolymer in the base polymer, the adhesive exhibits appropriate adhesive strength and good peelability, and can prevent changes in adhesive properties over time. When the content of the ethylene-α-olefin copolymer is more than 50% by weight, the adhesive strength exceeds 10 to 70 gf (98.1 to 687 mN) which is an appropriate range. This is not preferable because fuzz is generated on the surface, the thermal adhesive layer becomes too soft, and the adhesive adheres to the sealing iron during pressure bonding with a taping machine. When the ethylene-α-olefin copolymer is contained in the base polymer, for example, as the other polymer, an ethylene-vinyl acetate copolymer resin having a vinyl acetate content of 15% by weight or less, or the vinyl acetate content of 15% by weight. It is preferable to use low density polyethylene in addition to the ethylene-vinyl acetate copolymer resin which is not more than%. Preferred blending amounts in this case are, for example, low density polyethylene: 0 to 10% by weight, ethylene acetate vinyl resin having a vinyl acetate content of 15% by weight or less: 50 to 95% by weight, ethylene-α-olefin copolymer Polymer: 5 to 40% by weight.
粘着付与樹脂としては、例えば、石油樹脂(脂肪族石油樹脂、芳香族石油樹脂、前期芳香族石油樹脂を水添した脂環族石油樹脂など)、ロジン系樹脂、テルペン樹脂、スチレン樹脂、クマロン・インデン樹脂などが挙げられる。これらの粘着付与樹脂は単独又は、2種以上組み合わせて使用できる。なお、接着剤層を押出ラミネートにより形成する場合には、高温で溶融酸化されるので、酸化に対する安定性の点から、脂環族石油樹脂が特に好ましい。 Examples of tackifying resins include petroleum resins (aliphatic petroleum resins, aromatic petroleum resins, alicyclic petroleum resins hydrogenated with the previous aromatic petroleum resin, etc.), rosin resins, terpene resins, styrene resins, coumarone And indene resin. These tackifier resins can be used alone or in combination of two or more. In the case where the adhesive layer is formed by extrusion lamination, alicyclic petroleum resin is particularly preferable from the viewpoint of stability against oxidation because it is melted and oxidized at a high temperature.
接着剤層に粘着付与樹脂を含有することにより、テーピング作業性が向上するとともにキャリアテープなどの包装基材に対して安定かつ良好な接着力が得られる。 By including a tackifier resin in the adhesive layer, taping workability is improved and a stable and good adhesive force is obtained for a packaging substrate such as a carrier tape.
粘着付与樹脂の配合量は、ベースポリマー100重量部に対して1〜20重量部、好ましくは2〜13重量部、特に好ましくは3〜10重量部程度である。粘着付与樹脂が1重量部未満の場合は、キャリアテープ(包装基材)との接着性が得られにくい。また、20重量部を超えると、キャリアテープとの接着性は良いが、剥離の際、紙製包装基材表面より紙の繊維を引きちぎり、毛羽の発生につながり、回路基板製造工程においてエアーノズルでの吸着不良などの問題が発生する。また、接着力が著しく上昇して、規格である10〜70gf(98.1mN〜687mN)の適正接着力の範囲を外れてしまい、トップカバーテープとしての使用に適さないこととなる。 The compounding quantity of tackifying resin is 1-20 weight part with respect to 100 weight part of base polymers, Preferably it is 2-13 weight part, Most preferably, it is about 3-10 weight part. When the tackifying resin is less than 1 part by weight, it is difficult to obtain adhesion with a carrier tape (packaging substrate). On the other hand, if the amount exceeds 20 parts by weight, the adhesion to the carrier tape is good, but when peeling, the paper fibers are torn off from the surface of the paper packaging substrate, leading to the generation of fuzz. Problems such as poor adsorption at the surface occur. In addition, the adhesive strength is remarkably increased, and the range of the appropriate adhesive strength of 10 to 70 gf (98.1 mN to 687 mN), which is the standard, is out of the range, so that it is not suitable for use as a top cover tape.
高分子型帯電防止剤の配合量は、ベースポリマー100重量部に対して1〜30重量部、好ましくは10〜30重量部、特に好ましくは15〜25重量部である。高分子型帯電防止剤の配合量が少ない場合は、所望の帯電防止性能が得られず、表面抵抗率が1013Ω/□を超えることとなり、極少のチップ部品では、静電気による接着剤層への付着などの問題が発生する。また、高分子型帯電防止剤の配合割合が多すぎると、帯電防止性能は良好となるが、接着性能の低下をまねき、所望の接着力が得られない。なお、高分子型帯電防止剤に加えて、一般に使用される低分子型帯電防止剤(界面活性剤)を併用して表面抵抗率を調整することも可能である。この際の低分子型帯電防止剤の使用量は特に制限されないが、ベースポリマー100重量部に対して、例えば5重量部を超えない範囲内で適宜選択することができる。低分子型帯電防止剤の配合量が多すぎると、低分子型帯電防止剤が熱接着剤層表面にブリードするなどの問題が発生する場合があり、好ましくない。 The compounding amount of the polymer type antistatic agent is 1 to 30 parts by weight, preferably 10 to 30 parts by weight, particularly preferably 15 to 25 parts by weight with respect to 100 parts by weight of the base polymer. When the amount of the polymeric antistatic agent is small, the desired antistatic performance cannot be obtained, and the surface resistivity exceeds 10 13 Ω / □. Problems such as sticking occur. On the other hand, if the blending ratio of the polymer type antistatic agent is too large, the antistatic performance will be good, but the adhesive performance will be lowered and the desired adhesive strength will not be obtained. In addition to the polymer antistatic agent, it is also possible to adjust the surface resistivity by using a commonly used low molecular antistatic agent (surfactant). The amount of the low molecular weight antistatic agent used in this case is not particularly limited, but can be appropriately selected within a range not exceeding 5 parts by weight with respect to 100 parts by weight of the base polymer. If the amount of the low molecular weight antistatic agent is too large, problems such as bleeding of the low molecular weight antistatic agent to the surface of the thermal adhesive layer may occur.
高分子型帯電防止剤としては、帯電防止性を有するポリマーを何れも使用することができ、特に限定されない。例えば、ポリエーテルエステルアミドなどのポリアミド系コポリマー、カリウムアイオノマーなどのカルボン酸塩基含有ポリマー、第4級アンモニウム塩基含有コポリマーなどが挙げられる。高分子型帯電防止剤は、低分子型の帯電防止剤のように接着剤層内を移動し、接着剤層表面に浮き出ることなどがないため、高分子型帯電防止剤を使用することにより、長期にわたり安定した帯電防止性と接着性が得られる。例えば、接着剤層の表面抵抗率を1013Ω/□以下(例えば、108〜1013Ω/□程度)、好ましくは109〜1012Ω/□程度とすることができる。また、接着力についても適正な接着力である10〜70gf(98.1mN〜687mN)を長期にわたり安定して維持することができる。 As the polymer type antistatic agent, any polymer having antistatic properties can be used and is not particularly limited. Examples thereof include polyamide-based copolymers such as polyether ester amide, carboxylate group-containing polymers such as potassium ionomer, and quaternary ammonium base-containing copolymers. The polymer type antistatic agent moves in the adhesive layer unlike the low molecular type antistatic agent and does not float on the surface of the adhesive layer, so by using the polymer type antistatic agent, Stable antistatic properties and adhesion can be obtained over a long period of time. For example, the surface resistivity of the adhesive layer can be 10 13 Ω / □ or less (for example, about 10 8 to 10 13 Ω / □), preferably about 10 9 to 10 12 Ω / □. Moreover, 10-70 gf (98.1 mN-687 mN) which is an appropriate adhesive force can also be stably maintained over a long period of time.
高分子型帯電防止剤としては、例えばポリエーテルエステルアミド;ポリオレフィンとポリエーテルのブロックポリマー;ポリエチレンエーテル及びグリコールからなるポリマーなどのポリエーテル構造を含む高分子型帯電防止剤を好適に使用することができる。ポリエーテル構造を含む高分子型帯電防止剤を用いると、包装材用積層テープを包装基材に熱シールした後剥離する際に、ポリエーテル成分が基材側に残留し、接着剤中の帯電防止剤の一部が包装基材表面に転写されたかたちとなるため、包装基材の種類(素材)によらず、高い帯電防止効果を発揮することができる。例えば、本発明の包装材用積層テープを紙製包装基材に熱シールした後、紙製包装基材から剥離させた際の熱接着剤層に生じる剥離帯電圧の絶対値(23℃×65%RH、剥離角度180°、剥離速度5000mm/分、電極と接着剤層との距離5mm)は、どのような紙製包装基材を使用した場合であっても200V以下である。 As the polymer type antistatic agent, for example, polyether ester amide; block polymer of polyolefin and polyether; polymer type antistatic agent containing a polyether structure such as a polymer composed of polyethylene ether and glycol is preferably used. it can. When a polymer type antistatic agent containing a polyether structure is used, when the laminated tape for packaging material is heat-sealed to the packaging substrate and then peeled off, the polyether component remains on the substrate side, and the charge in the adhesive Since a part of the inhibitor is transferred to the surface of the packaging substrate, a high antistatic effect can be exhibited regardless of the type (material) of the packaging substrate. For example, after heat-sealing the laminated tape for packaging material of the present invention to a paper packaging substrate, the absolute value (23 ° C. × 65) of the stripping voltage generated in the thermal adhesive layer when peeled from the paper packaging substrate % RH, peeling angle 180 °, peeling speed 5000 mm / min, distance between the electrode and the adhesive layer 5 mm) is 200 V or less even when any paper packaging substrate is used.
また、剥離時にポリエーテル成分が基材側に残留することにより、一般に普及しているいかなる紙製包装基材に対しても、一定の条件で熱シールした場合には一定の接着力を発現する。例えば、本発明の包装材用積層テープを北越製紙製紙製包装基材:商品名「HOCTO40」及紙び北越製紙製紙製包装基材:商品名「HOCTO40E」に190℃で熱シールした場合、紙製包装基材「HOCTO40E」に対する接着力は、紙製包装基材「HOCTO40」に対する接着力の2倍以内である。なお、本発明者の検討によれば、紙製包装基材「HOCTO40」は、一般に普及している紙製包装基材のなかで、高分子型帯電防止剤を含まず、低分子型帯電防止剤を含む接着剤に対して最も低い接着力を示し、紙製包装基材「HOCTO40E」は、高分子型帯電防止剤を含まず、低分子型帯電防止剤を含む接着剤に対して最も高い接着力を示す。例えば、富士共和製紙製:商品名「FK−42」、東京製紙製:商品名「TK−43」、王子製紙製:商品名「HJ−42」などの一般に普及している紙製包装基材に本発明の包装材用積層テープを190℃で熱シールした際の接着力は、何れも本発明の包装材用積層テープを紙製包装基材「HOCTO40E」に190℃で熱シールした際の接着力以下であり、かつ本発明の包装材用積層テープを紙製包装基材「HOCTO40」に190℃で熱シールした際の接着力の2倍以下である。 In addition, since the polyether component remains on the substrate side at the time of peeling, it exhibits a certain adhesive force when heat-sealed under certain conditions to any commonly used paper packaging substrate. . For example, when the laminated tape for packaging material of the present invention is heat-sealed at 190 ° C. to Hokuetsu Papermaking Packaging Base: Trade Name “HOCTO40” and Hokuetsu Papermaking Packaging Base: Tradename “HOCTO40E” The adhesive strength to the packaging base material “HOCTO40E” is within twice the adhesive strength to the paper packaging base material “HOCTO40”. According to the study of the present inventor, the paper packaging substrate “HOCTO40” is a low-molecular-type antistatic agent that does not contain a polymer-type antistatic agent among the paper packaging substrates that are widely used. The paper packaging substrate “HOCTO40E” does not contain a high molecular weight antistatic agent and is the highest for an adhesive containing a low molecular weight antistatic agent. Indicates adhesive strength. For example, commonly used paper packaging substrates such as Fuji Kyowa Paper: trade name “FK-42”, Tokyo Paper: trade name “TK-43”, and Oji Paper: trade name “HJ-42”. The adhesive strength when heat-sealing the laminated tape for packaging material of the present invention at 190 ° C. is the same as when the laminated tape for packaging material of the present invention is heat-sealed at 190 ° C. to the paper packaging substrate “HOCTO40E”. The adhesive strength is less than or equal to twice the adhesive strength when the laminated tape for packaging material of the present invention is heat-sealed to a paper packaging substrate “HOCTO40” at 190 ° C.
ポリエーテル構造を含む高分子型帯電防止剤は公知慣用のものを使用することができ、特に制限されないが、ポリエーテルエステルアミドを含む高分子型帯電防止剤を特に好適に使用できる。例えば、両末端にカルボキシル基を有するポリアミドとポリ(オキシアルキレン)グリコールとの反応により得られ、平均分子量が8000〜100000程度のポリエーテルエステルアミドからなる高分子型帯電防止剤などを例示できる。高分子型帯電防止剤は、ベースポリマーや粘着付与樹脂の種類等により、相溶性やその他の物性を考慮して、適宜選択して使用すればよい。なお、高分子型帯電防止剤は、押出しラミネートや熱シールの際の高温による変質などを防止するために、熱分解温度が120℃以上であることが好ましい。 As the polymer type antistatic agent containing a polyether structure, known and commonly used ones can be used. Although not particularly limited, a polymer type antistatic agent containing a polyether ester amide can be particularly preferably used. For example, a polymer type antistatic agent obtained by a reaction of a polyamide having carboxyl groups at both ends and poly (oxyalkylene) glycol and comprising a polyether ester amide having an average molecular weight of about 8000 to 100,000 can be exemplified. The polymer type antistatic agent may be appropriately selected and used in consideration of compatibility and other physical properties depending on the type of base polymer and tackifying resin. The polymer antistatic agent preferably has a thermal decomposition temperature of 120 ° C. or higher in order to prevent deterioration due to high temperature during extrusion lamination or heat sealing.
粘着付与樹脂及び高分子型帯電防止剤の配合量は、それぞれ上述の範囲内で選択すればよいが、粘着付与樹脂及び高分子型帯電防止剤の添加量の総和がベースポリマー100重量部に対して好ましくは33重量部以下、さらに好ましくは30重量部以下となるような範囲で選択するのが望ましい。粘着付与樹脂及び高分子型帯電防止剤の添加量の総和がこの範囲内であると、接着力や表面抵抗率などの特性の経時変化がさらに抑制された包装材用積層テープが得られるため、好ましい。 The blending amounts of the tackifying resin and the polymer type antistatic agent may be selected within the above-mentioned ranges, respectively, but the total addition amount of the tackifying resin and the polymer type antistatic agent is 100 parts by weight of the base polymer. It is desirable to select within a range of preferably 33 parts by weight or less, more preferably 30 parts by weight or less. When the total amount of addition of the tackifying resin and the polymer antistatic agent is within this range, a laminated tape for a packaging material in which changes over time in properties such as adhesive force and surface resistivity are further suppressed can be obtained. preferable.
また、接着剤層の構成成分として、必要に応じて酸化防止剤、紫外線防止剤、カップリング剤の他、製造時の易加工性を考慮して、離型剤、フィラーなどを添加できる。更に、前記以外の帯電防止剤などを併用して使用することもできる。 In addition to an antioxidant, an ultraviolet ray inhibitor, and a coupling agent, as a constituent component of the adhesive layer, a mold release agent, a filler, and the like can be added in consideration of easy processability during production. Furthermore, antistatic agents other than those described above can be used in combination.
上述のベースポリマー、粘着付与樹脂、高分子型帯電防止剤及び必要に応じて配合されるその他の成分を溶融混合することにより本発明の包装材用積層テープの接着剤層を構成する接着剤組成物が得られる。この接着剤組成物は、該接着剤組成物を粒径約3mmのペレット状に成形し、35℃×80%RHの条件にした恒温恒湿機中に24時間保存した際の水分率が0.5%以下、特に0.3%以下であることが好ましい。吸湿後の水分率がこの範囲内であると、接着剤層が該接着剤よりなる包装材用積層テープは、環境の変化による接着力の変動が特に抑制されており、所望の接着力安定的に持続する。とりわけ、高湿度下や結露時における接着力の低下は上記水分率範囲内において顕著に抑制される。 Adhesive composition constituting the adhesive layer of the laminated tape for packaging material of the present invention by melt-mixing the above base polymer, tackifying resin, polymer antistatic agent and other components blended as necessary Things are obtained. This adhesive composition has a moisture content of 0 when the adhesive composition is formed into a pellet having a particle size of about 3 mm and stored in a thermostatic chamber at 35 ° C. × 80% RH for 24 hours. 0.5% or less, and particularly preferably 0.3% or less. When the moisture content after moisture absorption is within this range, the adhesive tape has an adhesive layer made of the adhesive, and the adhesive strength variation due to environmental changes is particularly suppressed, and the desired adhesive strength is stable. To last. In particular, a decrease in adhesive strength under high humidity and condensation is remarkably suppressed within the above moisture content range.
上記成分により構成される接着剤層の厚さは、接着性やハンドリング性などの点から5〜50μm、特に10〜30μm程度が好ましい。接着剤層の厚さが5μm未満では十分な接着力が得られない場合があり、50μmより厚いと熱シール時に接着剤が染みだしてテーピングマシン等を汚染するトラブルが発生する場合がある。 The thickness of the adhesive layer composed of the above components is preferably 5 to 50 μm, particularly preferably about 10 to 30 μm from the viewpoints of adhesion and handling properties. If the thickness of the adhesive layer is less than 5 μm, sufficient adhesive strength may not be obtained. If the thickness is greater than 50 μm, the adhesive may ooze out during heat sealing, causing troubles that contaminate the taping machine or the like.
本発明では、前記支持基材層と接着剤層の間に、両者の密着性を向上するために、中間層を設けることもできる。この中間層は、例えば、ポリオレフィン系樹脂などの熱可塑性樹脂、熱可塑性エラストマー、などで構成できる。これらの成分は単独で又は2種以上混合して使用できる。ポリオレフィン系樹脂、熱可塑性エラストマーとしては前記例示のものを使用できる。 In this invention, in order to improve both adhesiveness between the said support base material layer and an adhesive bond layer, an intermediate | middle layer can also be provided. This intermediate layer can be composed of, for example, a thermoplastic resin such as a polyolefin-based resin, a thermoplastic elastomer, or the like. These components can be used alone or in admixture of two or more. As the polyolefin resin and the thermoplastic elastomer, those exemplified above can be used.
中間層の厚みとしては、製造工程における作業性や、積層テープとしたときの取り扱い性を損なわない範囲内で適宜選択できるが、例えばラミネート法により製造する場合であれば、5μm〜30μm程度が一般的である。 The thickness of the intermediate layer can be appropriately selected within the range that does not impair the workability in the manufacturing process and the handling property when it is made into a laminated tape. For example, when manufactured by a laminating method, the thickness is generally about 5 μm to 30 μm. Is.
本発明の積層テープは、例えば、接着剤層の構成成分を所定の割合で配合し、二軸混練機でメルトブレンドしてペレット化したもの、またはドライブレンドしたものを慣用のシングル又はタンデム押出しラミネート法により、支持基材上に中間層を介し、又は介さずにラミネートすることにより製造できる。また、接着剤層と中間層とを支持基材層上に共押出しラミネートにより積層して製造することもできる。 The laminated tape of the present invention is, for example, a conventional single or tandem extrusion laminate in which the constituent components of the adhesive layer are blended at a predetermined ratio, melt blended with a twin-screw kneader, pelletized, or dry blended. According to the method, it can be produced by laminating on a supporting substrate with or without an intermediate layer. Moreover, it can also manufacture by laminating | stacking an adhesive bond layer and an intermediate | middle layer on a support base material layer by coextrusion lamination.
このようにして得られる積層テープは、チップ固定抵抗器などの抵抗器、積層セラミックコンデンサなどのチップ型電子部品を搬送する際の包装材用積層テープ等として好適に使用できる。特に、紙製包装基材に熱シールした後、剥離する際の剥離性に優れており、紙製包装基材表層の紙繊維を毛羽立たせることなしに剥離することができる。 The laminated tape thus obtained can be suitably used as a laminated tape for a packaging material when a chip-type electronic component such as a resistor such as a chip-fixed resistor or a laminated ceramic capacitor is conveyed. In particular, after heat-sealing to a paper packaging substrate, it has excellent releasability when peeling, and can be peeled without fluffing the paper fibers on the surface of the paper packaging substrate.
以下、本発明を実施例に基づいてより詳細に説明するが、本発明はこれらの実施例により何ら限定されるものではない。なお、実施例2は参考例として記載するものである。
EXAMPLES Hereinafter, although this invention is demonstrated in detail based on an Example, this invention is not limited at all by these Examples. In addition, Example 2 is described as a reference example.
(実施例1)
ベースポリマーとして、エチレン−酢酸ビニル共重合体(EVA)(三井石油化学工業(株)製:商品名「ミラソンMV0603」)80重量部;エチレン−α−オレフィン共重合体20重量部、脂環族系石油樹脂(荒川化学工業(株)製:商品名「アルコンP−125」)10重量部、ポリエーテル構造を含む高分子型帯電防止剤(三光化学工業(株)製:商品名「サンコノールTBX−310」)5重量部を2軸混練機にてメルトブレンドして溶融物を調製した。支持基材(厚み25μmのポリエステルフィルム)上に、押出ラミネート加工により、低密度ポリエチレン(LDPE)(三井石油化学工業(株)製:商品名「ミラソン16P」)からなる厚さ15μmの中間層を設け、さらにこの中間層の上に上記溶融物を、厚みが20μmとなるように溶融押出しして熱接着剤層を設け、支持基材、中間層及び熱接着剤層よりなる積層テープを得た。
Example 1
As a base polymer, ethylene-vinyl acetate copolymer (EVA) (manufactured by Mitsui Petrochemical Co., Ltd .: trade name “Mirason MV0603”) 80 parts by weight; ethylene-α-olefin copolymer 20 parts by weight, alicyclic -Based petroleum resin (Arakawa Chemical Industries, Ltd .: trade name “Arcon P-125”), 10 parts by weight, a polymer type antistatic agent containing a polyether structure (Sanko Chemical Industries, Ltd .: trade name “Sanconol TBX”) -310 ") 5 parts by weight were melt blended in a twin-screw kneader to prepare a melt. An intermediate layer having a thickness of 15 μm made of low-density polyethylene (LDPE) (trade name “Mirason 16P” manufactured by Mitsui Petrochemical Co., Ltd.) is formed on a supporting substrate (polyester film having a thickness of 25 μm) by extrusion lamination. Furthermore, the above melt was melt-extruded on this intermediate layer so as to have a thickness of 20 μm to provide a thermal adhesive layer, and a laminated tape comprising a support substrate, an intermediate layer and a thermal adhesive layer was obtained. .
(実施例2)
ベースポリマーとして、エチレン−酢酸ビニル共重合体(EVA)(三井石油化学工業(株)製:商品名「ミラソンMV0603」)100重量部、脂環族系石油樹脂(荒川化学工業(株)製:商品名「アルコンP−125」)15重量部、高分子型帯電防止剤としてポリエーテルエステルアミド(三洋化成工業(株)製:商品名「ペレスタット230」)1重量部、低分子型帯電防止剤(花王(株)製:商品名「TS−3B」)1重量部を2軸混練機にてメルトブレンドして溶融物を調製した。支持基材(厚み25μmのポリエステルフィルム)上に、押出ラミネート加工により、低密度ポリエチレン(LDPE)(三井石油化学工業(株)製:商品名「ミラソン16P」)からなる厚さ15μmの中間層を設け、さらにこの中間層の上に上記溶融物を、厚みが20μmとなるように溶融押出しして熱接着剤層を設け、支持基材、中間層及び熱接着剤層よりなる積層テープを得た。
(Example 2)
As a base polymer, ethylene-vinyl acetate copolymer (EVA) (manufactured by Mitsui Petrochemical Industries, Ltd .: trade name “Mirason MV0603”), 100 parts by weight, alicyclic petroleum resin (manufactured by Arakawa Chemical Industries, Ltd.): 15 parts by weight of a trade name “Arcon P-125”, 1 part by weight of a polyether ester amide (manufactured by Sanyo Kasei Kogyo Co., Ltd .: trade name “Pelestat 230”) as a polymer antistatic agent, a low molecular antistatic agent A melt was prepared by melt blending 1 part by weight (trade name “TS-3B”, manufactured by Kao Corporation) with a biaxial kneader. An intermediate layer having a thickness of 15 μm made of low-density polyethylene (LDPE) (trade name “Mirason 16P” manufactured by Mitsui Petrochemical Co., Ltd.) is formed on a supporting substrate (polyester film having a thickness of 25 μm) by extrusion lamination. Furthermore, the above melt was melt-extruded on this intermediate layer so as to have a thickness of 20 μm to provide a thermal adhesive layer, and a laminated tape comprising a support substrate, an intermediate layer and a thermal adhesive layer was obtained. .
(実施例3)
ベースポリマーとして、エチレン−酢酸ビニル共重合体(EVA)(三井石油化学工業(株)製:商品名「ミラソンMV0603」)70重量部;エチレン−α−オレフィン共重合体30重量部、脂環族系石油樹脂(荒川化学工業(株)製:商品名「アルコンP−125」)5重量部、高分子型帯電防止剤としてポリエーテルエステルアミド(三洋化成工業(株)製:商品名「ペレスタット230」)20重量部を2軸混練機にてメルトブレンドして溶融物を調製した。支持基材(厚み25μmのポリエステルフィルム)上に、押出ラミネート加工により、低密度ポリエチレン(LDPE)(三井石油化学工業(株)製:商品名「ミラソン16P」)からなる厚さ15μmの中間層を設け、さらにこの中間層の上に上記溶融物を、厚みが20μmとなるように溶融押出しして熱接着剤層を設け、支持基材、中間層及び熱接着剤層よりなる積層テープを得た。
Example 3
As a base polymer, ethylene-vinyl acetate copolymer (EVA) (manufactured by Mitsui Petrochemical Co., Ltd .: trade name “Mirason MV0603”) 70 parts by weight; ethylene-α-olefin copolymer 30 parts by weight, alicyclic -Based petroleum resin (Arakawa Chemical Industries, Ltd .: trade name “Alcon P-125”) 5 parts by weight, polyether ester amide (manufactured by Sanyo Chemical Industries, Ltd .: trade name “Pelestat 230” as a polymer type antistatic agent) ]) 20 parts by weight was melt-blended with a twin-screw kneader to prepare a melt. An intermediate layer having a thickness of 15 μm made of low-density polyethylene (LDPE) (trade name “Mirason 16P” manufactured by Mitsui Petrochemical Co., Ltd.) is formed on a supporting substrate (polyester film having a thickness of 25 μm) by extrusion lamination. Furthermore, the above melt was melt-extruded on this intermediate layer so as to have a thickness of 20 μm to provide a thermal adhesive layer, and a laminated tape comprising a support substrate, an intermediate layer and a thermal adhesive layer was obtained. .
(実施例4)
ベースポリマーとして、エチレン−酢酸ビニル共重合体(EVA)(三井石油化学工業(株)製:商品名「ミラソンMV0603」)90重量部;エチレン−α−オレフィン共重合体10重量部、脂環族系石油樹脂(荒川化学工業(株)製:商品名「アルコンP−125」)10重量部、高分子型帯電防止剤としてポリエーテルエステルアミド(三洋化成工業(株)製:商品名「ペレスタット230」)20重量部を2軸混練機にてメルトブレンドして溶融物を調製した。支持基材(厚み25μmのポリエステルフィルム)上に、押出ラミネート加工により、低密度ポリエチレン(LDPE)(三井石油化学工業(株)製:商品名「ミラソン16P」)からなる厚さ15μmの中間層を設け、さらにこの中間層の上に上記溶融物を、厚みが20μmとなるように溶融押出しして熱接着剤層を設け、支持基材、中間層及び熱接着剤層よりなる積層テープを得た。
(Example 4)
As a base polymer, ethylene-vinyl acetate copolymer (EVA) (manufactured by Mitsui Petrochemical Co., Ltd .: trade name “Mirason MV0603”) 90 parts by weight; ethylene-α-olefin copolymer 10 parts by weight, alicyclic -Based petroleum resin (Arakawa Chemical Industries, Ltd .: trade name “Alcon P-125”), 10 parts by weight of polyether ester amide (manufactured by Sanyo Chemical Industries, Ltd .: trade name “Pelestat 230”) ]) 20 parts by weight was melt-blended with a twin-screw kneader to prepare a melt. An intermediate layer having a thickness of 15 μm made of low-density polyethylene (LDPE) (trade name “Mirason 16P” manufactured by Mitsui Petrochemical Co., Ltd.) is formed on a supporting substrate (polyester film having a thickness of 25 μm) by extrusion lamination. Furthermore, the above melt was melt-extruded on this intermediate layer so as to have a thickness of 20 μm to provide a thermal adhesive layer, and a laminated tape comprising a support substrate, an intermediate layer and a thermal adhesive layer was obtained. .
(実施例5)
ベースポリマーとして、エチレン−酢酸ビニル共重合体(EVA)(三井石油化学工業(株)製:商品名「ミラソンMV0603」)90重量部;エチレン−α−オレフィン共重合体10重量部、脂環族系石油樹脂(荒川化学工業(株)製:商品名「アルコンP−125」)10重量部、高分子型帯電防止剤としてポリエーテルエステルアミド(三洋化成工業(株)製:商品名「ペレスタット212」)20重量部を2軸混練機にてメルトブレンドして溶融物を調製した。支持基材(厚み25μmのポリエステルフィルム)上に、押出ラミネート加工により、低密度ポリエチレン(LDPE)(三井石油化学工業(株)製:商品名「ミラソン16P」)からなる厚さ15μmの中間層を設け、さらにこの中間層の上に上記溶融物を、厚みが20μmとなるように溶融押出しして熱接着剤層を設け、支持基材、中間層及び熱接着剤層よりなる積層テープを得た。
(Example 5)
As a base polymer, ethylene-vinyl acetate copolymer (EVA) (manufactured by Mitsui Petrochemical Co., Ltd .: trade name “Mirason MV0603”) 90 parts by weight; ethylene-α-olefin copolymer 10 parts by weight, alicyclic -Based petroleum resin (Arakawa Chemical Industries, Ltd .: trade name “Alcon P-125”), 10 parts by weight of polyether ester amide (manufactured by Sanyo Chemical Industries, Ltd .: trade name “Pelestat 212” as a polymer type antistatic agent) ]) 20 parts by weight was melt-blended with a twin-screw kneader to prepare a melt. An intermediate layer having a thickness of 15 μm made of low-density polyethylene (LDPE) (trade name “Mirason 16P” manufactured by Mitsui Petrochemical Co., Ltd.) is formed on a supporting substrate (polyester film having a thickness of 25 μm) by extrusion lamination. Furthermore, the above melt was melt-extruded on this intermediate layer so as to have a thickness of 20 μm to provide a thermal adhesive layer, and a laminated tape comprising a support substrate, an intermediate layer and a thermal adhesive layer was obtained. .
(比較例1)
ベースポリマーとして、エチレン−酢酸ビニル共重合体(EVA)(三井石油化学工業(株)製:商品名「ミラソンMV0603」)100重量部、脂環族系石油樹脂(荒川化学工業(株)製:商品名「アルコンP−125」)15重量部、高分子型帯電防止剤としてポリエーテルエステルアミド(三洋化成工業(株)製:商品名「ペレスタット230」)0.5重量部、低分子型帯電防止剤(花王(株)製:商品名「TS−3B」)1重量部を2軸混練機にてメルトブレンドして溶融物を調製した。支持基材(厚み25μmのポリエステルフィルム)上に、押出ラミネート加工により、低密度ポリエチレン(LDPE)(三井石油化学工業(株)製:商品名「ミラソン16P」)からなる厚さ15μmの中間層を設け、さらにこの中間層の上に上記溶融物を、厚みが20μmとなるように溶融押出しして熱接着剤層を設け、支持基材、中間層及び熱接着剤層よりなる積層テープを得た。
(Comparative Example 1)
As a base polymer, ethylene-vinyl acetate copolymer (EVA) (manufactured by Mitsui Petrochemical Industries, Ltd .: trade name “Mirason MV0603”), 100 parts by weight, alicyclic petroleum resin (manufactured by Arakawa Chemical Industries, Ltd.): Product name “Arcon P-125”) 15 parts by weight, polyether ester amide (manufactured by Sanyo Kasei Kogyo Co., Ltd .: trade name “Perestat 230”) as polymer type antistatic agent, 0.5 part by weight, low molecular charge One part by weight of an inhibitor (trade name “TS-3B” manufactured by Kao Corporation) was melt blended with a twin-screw kneader to prepare a melt. An intermediate layer having a thickness of 15 μm made of low-density polyethylene (LDPE) (trade name “Mirason 16P” manufactured by Mitsui Petrochemical Co., Ltd.) is formed on a supporting substrate (polyester film having a thickness of 25 μm) by extrusion lamination. Furthermore, the above melt was melt-extruded on this intermediate layer so as to have a thickness of 20 μm to provide a thermal adhesive layer, and a laminated tape comprising a support substrate, an intermediate layer and a thermal adhesive layer was obtained. .
(比較例2)
ベースポリマーとして、エチレン−酢酸ビニル共重合体(EVA)(三井石油化学工業(株)製:商品名「ミラソンMV0603」)100重量部、脂環族系石油樹脂(荒川化学工業(株)製:商品名「アルコンP−125」)15重量部、低分子型帯電防止剤(花王(株)製:商品名「TS−3B」)1重量部を2軸混練機にてメルトブレンドして溶融物を調製した。支持基材(厚み25μmのポリエステルフィルム)上に、押出ラミネート加工により、低密度ポリエチレン(LDPE)(三井石油化学工業(株)製:商品名「ミラソン16P」)からなる厚さ15μmの中間層を設け、さらにこの中間層の上に上記溶融物を、厚みが20μmとなるように溶融押出しして熱接着剤層を設け、支持基材、中間層及び熱接着剤層よりなる積層テープを得た。
(Comparative Example 2)
As a base polymer, ethylene-vinyl acetate copolymer (EVA) (manufactured by Mitsui Petrochemical Industries, Ltd .: trade name “Mirason MV0603”), 100 parts by weight, alicyclic petroleum resin (manufactured by Arakawa Chemical Industries, Ltd.): 15 parts by weight of trade name “Arcon P-125”) and 1 part by weight of low molecular weight antistatic agent (trade name “TS-3B” manufactured by Kao Corporation) are melt-blended in a twin-screw kneader. Was prepared. An intermediate layer having a thickness of 15 μm made of low-density polyethylene (LDPE) (trade name “Mirason 16P” manufactured by Mitsui Petrochemical Co., Ltd.) is formed on a supporting substrate (polyester film having a thickness of 25 μm) by extrusion lamination. Furthermore, the above melt was melt-extruded on this intermediate layer so as to have a thickness of 20 μm to provide a thermal adhesive layer, and a laminated tape comprising a support substrate, an intermediate layer and a thermal adhesive layer was obtained. .
(比較例3)
ベースポリマーとして、エチレン−酢酸ビニル共重合体(EVA)(三井石油化学工業(株)製:商品名「ミラソンMV0603」)100重量部、脂環族系石油樹脂(荒川化学工業(株)製:商品名「アルコンP−125」)40重量部、高分子型帯電防止剤としてポリエーテルエステルアミド(三洋化成工業(株)製:商品名「ペレスタット230」)20重量部を2軸混練機にてメルトブレンドして溶融物を調製した。支持基材(厚み25μmのポリエステルフィルム)上に、押出ラミネート加工により、低密度ポリエチレン(LDPE)(三井石油化学工業(株)製:商品名「ミラソン16P」)からなる厚さ15μmの中間層を設け、さらにこの中間層の上に上記溶融物を、厚みが20μmとなるように溶融押出しして熱接着剤層を設け、支持基材、中間層及び熱接着剤層よりなる積層テープを得た。
(Comparative Example 3)
As a base polymer, ethylene-vinyl acetate copolymer (EVA) (manufactured by Mitsui Petrochemical Industries, Ltd .: trade name “Mirason MV0603”), 100 parts by weight, alicyclic petroleum resin (manufactured by Arakawa Chemical Industries, Ltd.): 40 parts by weight of a trade name “Arcon P-125”) and 20 parts by weight of a polyether ester amide (manufactured by Sanyo Kasei Kogyo Co., Ltd .: trade name “Perestat 230”) as a polymer type antistatic agent in a biaxial kneader A melt was prepared by melt blending. An intermediate layer having a thickness of 15 μm made of low-density polyethylene (LDPE) (trade name “Mirason 16P” manufactured by Mitsui Petrochemical Co., Ltd.) is formed on a supporting substrate (polyester film having a thickness of 25 μm) by extrusion lamination. Furthermore, the above melt was melt-extruded on this intermediate layer so as to have a thickness of 20 μm to provide a thermal adhesive layer, and a laminated tape comprising a support substrate, an intermediate layer and a thermal adhesive layer was obtained. .
(評価方法)
実施例及び比較例で得られた各積層テープにつき、下記の試験を行った。
[150℃接着力:ピール強度]
紙製包装基材(北越製紙製:商品名「HOCTO40」)の表面に、各積層テープをテーピングマシン(東京ウェルズ製:商品名「TWA−6600」)を用いて、1600PCS/min、圧着温度150℃の条件で熱シールし、熱シール直後及び40℃で1ヶ月間保存した後の接着力を測定した。なお、接着力の測定は、剥離試験機を用いて、剥離速度300mm/min 剥離角度約180°の条件で行った。実施例1、2及び比較例1についての結果を表1に、実施例3、4及び比較例2、3についての結果を表2にそれぞれ示す。なお、実施例1、2及び比較例1については熱シール直後のみ測定を行った。
[180℃接着力:ピール強度]
圧着温度を180℃とした以外は、150℃接着力の測定と同様にして熱シール直後及び40℃で1ヶ月間保存した後の接着力を測定した。実施例1、2及び比較例1についての結果を表1に、実施例3、4及び比較例2、3についての結果を表2にそれぞれ示す。なお、実施例1〜2及び比較例1については熱シール直後のみ測定を行った。
[表面抵抗率]
各積層テープにつき、製造時(初期)及び40℃で1ヶ月間保存後の接着剤層表面の表面抵抗率を、高抵抗率計(三菱化学(株)製:商品名「ハイレスターUP」で測定した。実施例1、2及び比較例1についての結果を表1に、実施例3、4及び比較例2、3についての結果を表2にそれぞれ示す。なお、実施例1〜2及び比較例1については熱シール直後のみ測定を行った。
[実装性試験]
各積層テープをトップカバーとして用いて熱シールして、チップ(0603タイプ)[2000PCS/試験片]をキャリアに封入した後、室温まで冷却した。23℃/50%RHにおいてトップカバーを剥離後実装機にかけたときの、エアーノズルで吸着できたチップの全チップ数に対する割合を求めた。また、チップを封入した後、23℃/30%RHで1ヶ月間保存した後、同様に実装機にかけ、エアーノズルにより吸着できたチップの割合を求めた。実施例1〜2及び比較例1についての結果を表1に、実施例3、4及び比較例2、3についての結果を表2にそれぞれ示す。なお、実施例1〜2及び比較例1については熱シール直後のみ測定を行った。
[毛羽発生確認]
実施例3、4及び比較例2、3で得られた各積層テープを紙製包装基材(北越製紙製:商品名「HOCTO40」、富士共和製紙製:商品名「FK−42」、東京製紙製:商品名「TK−43」、王子製紙製:商品名「HJ−42」)に対し、テーピングマシン(東京ウェルズ製:商品名「TWA−6600」)を用いて、1600PCS/minの条件で圧着温度150℃及び180℃にて熱シールしたテーピングサンプルを40℃にて1ヶ月間保存した後、引き剥がした際、接着剤層表面に紙の繊維が付着しているかどうかを目視にて確認した。結果を表3に示す。尚、評価は以下の基準で行った。○:紙製包装基材表層からの毛羽立ちは目視確認されなかった。△:0.5mm未満毛羽(紙繊維)を目視確認した。×:0.5mm以上の毛羽(紙繊維)を目視確認した。
[剥離帯電圧]
各積層テープを、紙製包装基材(北越製紙製:商品名「HOCTO40」、富士共和製紙製:商品名「FK−42」、東京製紙製:商品名「TK−43」、王子製紙製:商品名「HJ−42」、北越製紙製:商品名「HOCTO40E」)に対し、テーピングマシン(東京ウェルズ製:商品名「TWA−6600」)を用いて、1600PCS/minの条件で圧着温度180℃にて熱シールしてサンプルを作製した。このサンプルの包装材用積層テープ(カバーテープ)を23℃、65%RHの雰囲気下で、剥離試験機を用いて180°方向に剥離速度5000mm/分の速度で100mm引き剥がし、その時の接着剤層表面の静電気発生量[剥離帯電圧(V);表面電位]を、表面電位測定器(商品名「ELECTROSTATIC VOLTMETER」:トレック・ジャパン株式会社製)を用いて測定した。表面電位測定用プローブの高さは、接着剤層表面から約5mmとした。結果を表4に示す。表面電位(表面の静電気発生量)の測定値(V)の数値は実測値である。
[一般に普及している紙製包装基材に対する接着力]
実施例3及び比較例2で得られた包装用積層テープを、一般に普及している紙製包装基材に、テーピングマシン(東京ウェルズ製:商品名「TWA−6600」)を用いて、1600PCS/minの条件で圧着温度130℃、150℃、170℃、190℃で熱シールしてサンプルを作成した。このサンプルの包装材用積層テープを剥離試験機を用いて剥離速度300mm/min、剥離角度180°で剥離して接着力を測定した。なお、一般に普及している紙製包装基材として北越製紙製:商品名「HOCTO40」、富士共和製紙製:商品名「FK−42」、東京製紙製:商品名「TK−43」、王子製紙製:商品名「HJ−42」、北越製紙製:商品名「HOCTO40E」を使用した。結果を表5に示す。
[吸湿後接着力]
紙製包装基材(北越製紙製:商品名「HOCTO40」)の表面に、各積層テープをテーピングマシン(東京ウェルズ製:商品名「TWA−6600」)を用いて、1600PCS/min、圧着温度150℃及び180℃の条件で熱シールし、熱シール直後及び23℃×80%RHで1ヶ月間保存した後の接着力を測定した。なお、接着力の測定は、剥離試験機を用いて、剥離速度300mm/min 剥離角度約180°の条件で行った。結果を表6に示す。
[水分率]
実施例4、5及び比較例2で得られた接着剤層を調製するための溶融物を粒径約3mmのペレット状に成形し、サンプルとした。このサンプルを解放した瓶に入れ、35℃×80%RHの条件にした高温恒湿機中に24時間保存した後、サンプルの水分率を電量滴定式水分測定装置を用いて測定した。結果を表6に示す。
(Evaluation methods)
The following tests were performed on each laminated tape obtained in the examples and comparative examples.
[150 ° C adhesive strength: peel strength]
Using a taping machine (Tokyo Wells: trade name “TWA-6600”), each laminated tape is applied to the surface of a paper packaging substrate (Hokuetsu Paper: trade name “HOCTO40”) at a temperature of 1600 PCS / min. The film was heat-sealed under the condition of ° C., and the adhesive strength was measured immediately after the heat sealing and after storage for 1 month at 40 ° C. In addition, the measurement of adhesive force was performed on the conditions of a peeling speed of 300 mm / min and a peeling angle of about 180 ° using a peeling tester. The results for Examples 1 and 2 and Comparative Example 1 are shown in Table 1, and the results for Examples 3 and 4 and Comparative Examples 2 and 3 are shown in Table 2, respectively. For Examples 1 and 2 and Comparative Example 1, measurement was performed only immediately after heat sealing.
[180 ° C adhesive strength: peel strength]
The adhesive force was measured immediately after heat sealing and after storage at 40 ° C. for 1 month, except that the pressure bonding temperature was 180 ° C. The results for Examples 1 and 2 and Comparative Example 1 are shown in Table 1, and the results for Examples 3 and 4 and Comparative Examples 2 and 3 are shown in Table 2, respectively. In addition, about Examples 1-2 and the comparative example 1, it measured only immediately after heat sealing.
[Surface resistivity]
For each laminated tape, the surface resistivity of the adhesive layer surface at the time of manufacture (initial) and after storage at 40 ° C. for 1 month is measured with a high resistivity meter (Mitsubishi Chemical Co., Ltd. product name: “High Lester UP”). The results for Examples 1 and 2 and Comparative Example 1 are shown in Table 1, and the results for Examples 3 and 4 and Comparative Examples 2 and 3 are shown in Table 2. Examples 1-2 and Comparative For Example 1, measurements were made only immediately after heat sealing.
[Mountability test]
Each laminated tape was heat-sealed using a top cover to enclose a chip (0603 type) [2000 PCS / test piece] in a carrier, and then cooled to room temperature. When the top cover was peeled off at 23 ° C./50% RH and applied to the mounting machine, the ratio of the chips that could be adsorbed by the air nozzle to the total number of chips was determined. In addition, after encapsulating the chip, it was stored at 23 ° C./30% RH for 1 month, and similarly applied to a mounting machine to determine the ratio of the chip that could be adsorbed by the air nozzle. The results for Examples 1 and 2 and Comparative Example 1 are shown in Table 1, and the results for Examples 3 and 4 and Comparative Examples 2 and 3 are shown in Table 2, respectively. In addition, about Examples 1-2 and the comparative example 1, it measured only immediately after heat sealing.
[Fuzz generation confirmation]
Each laminated tape obtained in Examples 3 and 4 and Comparative Examples 2 and 3 was made of a paper packaging substrate (made by Hokuetsu Paper: trade name “HOCTO40”, manufactured by Fuji Kyowa Paper: trade name “FK-42”, Tokyo Paper Industries). Product: “TK-43”, product name “HJ-42” manufactured by Oji Paper Co., Ltd., using a taping machine (product name “TWA-6600” manufactured by Tokyo Wells) under the condition of 1600 PCS / min. Taping samples heat-sealed at 150 ° C and 180 ° C are stored at 40 ° C for 1 month, and when peeled off, it is visually checked whether paper fibers are attached to the adhesive layer surface. did. The results are shown in Table 3. The evaluation was performed according to the following criteria. ○: No fluffing from the surface of the paper packaging substrate was visually confirmed. Δ: Fluff (paper fiber) of less than 0.5 mm was visually confirmed. X: Fluff (paper fiber) of 0.5 mm or more was visually confirmed.
[Peeling voltage]
Each laminated tape is made of a paper packaging substrate (made by Hokuetsu Paper: trade name “HOCTO40”, made by Fuji Kyowa Paper: trade name “FK-42”, made by Tokyo Paper: trade name “TK-43”, made by Oji Paper: Using a taping machine (manufactured by Tokyo Wells: trade name “TWA-6600”) against a trade name “HJ-42”, Hokuetsu Paper: trade name “HOCTO40E”), a pressure bonding temperature of 180 ° C. under the condition of 1600 PCS / min. A sample was prepared by heat sealing at. The laminated tape (cover tape) for the packaging material of this sample is peeled off 100 mm at a peeling speed of 5000 mm / min in a 180 ° direction using a peeling tester in an atmosphere of 23 ° C. and 65% RH, and the adhesive at that time The amount of static electricity generated on the surface of the layer [peeling voltage (V); surface potential] was measured using a surface potential measuring device (trade name “ELECTROSTATIC VOLTMETER” manufactured by Trek Japan Co., Ltd.). The height of the surface potential measuring probe was about 5 mm from the surface of the adhesive layer. The results are shown in Table 4. The measured value (V) of the surface potential (the amount of static electricity generated on the surface) is an actually measured value.
[Adhesion to commonly used paper packaging substrates]
Using the taping machine (manufactured by Tokyo Wells: trade name “TWA-6600”), the laminated tape for packaging obtained in Example 3 and Comparative Example 2 on a widely used paper packaging substrate, 1600 PCS / Samples were prepared by heat-sealing at 130 ° C., 150 ° C., 170 ° C., and 190 ° C. under the conditions of min. The laminated tape for packaging material of this sample was peeled off at a peeling speed of 300 mm / min and a peeling angle of 180 ° using a peel tester, and the adhesive strength was measured. In addition, as a paper packaging base material that is widely used, Hokuetsu Paper Industries: trade name “HOCTO40”, Fuji Kyowa Paper: trade name “FK-42”, Tokyo Paper Industries: trade name “TK-43”, Oji Paper Product name: “HJ-42”, Hokuetsu Paper Industries: product name “HOCTO40E” was used. The results are shown in Table 5.
[Adhesive strength after moisture absorption]
Using a taping machine (Tokyo Wells: trade name “TWA-6600”), each laminated tape is applied to the surface of a paper packaging substrate (Hokuetsu Paper: trade name “HOCTO40”) at a temperature of 1600 PCS / min. The film was heat-sealed under the conditions of 180 ° C. and 180 ° C., and the adhesive force was measured immediately after the heat sealing and after storage at 23 ° C. × 80% RH for 1 month. In addition, the measurement of adhesive force was performed on the conditions of a peeling speed of 300 mm / min and a peeling angle of about 180 ° using a peeling tester. The results are shown in Table 6.
[Moisture percentage]
The melt for preparing the adhesive layers obtained in Examples 4 and 5 and Comparative Example 2 was formed into pellets having a particle size of about 3 mm to obtain samples. The sample was placed in an opened bottle and stored in a high-temperature humidity chamber under conditions of 35 ° C. × 80% RH for 24 hours, and then the moisture content of the sample was measured using a coulometric titration moisture measuring device. The results are shown in Table 6.
実施例5で得られた包装材用積層テープは、接着剤層が高湿度下で保存後の水分率が低い接着剤により構成されているので、適度な接着力を高湿度に保存した場合であっても長期間にわたり維持している。これに対して実施例4で得られた包装材用積層テープは、接着力、表面抵抗率ともに良好で、該良好な値を長期間にわたり維持しており、毛羽発生や剥離帯電圧についても良好な成績であるが、接着剤層が高湿度下で保存後の水分率が0.6%と高い接着剤により構成されているため、高湿度下で保存した場合は接着力が低下する。また、比較例2で得られた包装材用積層テープは、高湿度下で保存後の接着剤の水分率は低いが、高分子型帯電防止剤を含まないため接着力が経時的に変化し、特に高湿度下で保存した場合には接着力が著しく低下する。 The laminated tape for packaging material obtained in Example 5 is composed of an adhesive whose adhesive layer has a low moisture content after storage under high humidity, and therefore has an appropriate adhesive strength when stored at high humidity. Even if so, it is maintained for a long time. On the other hand, the laminated tape for packaging material obtained in Example 4 has good adhesive force and surface resistivity, maintains the good values over a long period of time, and has good fuzz generation and peeling voltage. Although it is a good result, since the adhesive layer is composed of an adhesive having a high moisture content of 0.6% after storage under high humidity, the adhesive strength decreases when stored under high humidity. In addition, the laminated tape for packaging material obtained in Comparative Example 2 has a low moisture content of the adhesive after storage under high humidity, but the adhesive strength changes with time because it does not contain a polymer type antistatic agent. In particular, when it is stored under high humidity, the adhesive strength is remarkably reduced.
Claims (2)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2008225174A JP4437505B2 (en) | 2005-05-19 | 2008-09-02 | Laminated tape for packaging materials |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2005146225 | 2005-05-19 | ||
JP2006073421 | 2006-03-16 | ||
JP2008225174A JP4437505B2 (en) | 2005-05-19 | 2008-09-02 | Laminated tape for packaging materials |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2006129827A Division JP4198163B2 (en) | 2005-05-19 | 2006-05-09 | Laminated tape for packaging materials |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2008285687A JP2008285687A (en) | 2008-11-27 |
JP4437505B2 true JP4437505B2 (en) | 2010-03-24 |
Family
ID=37706658
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2008086417A Expired - Fee Related JP5106208B2 (en) | 2005-05-19 | 2008-03-28 | Laminated tape for packaging materials |
JP2008225174A Expired - Fee Related JP4437505B2 (en) | 2005-05-19 | 2008-09-02 | Laminated tape for packaging materials |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2008086417A Expired - Fee Related JP5106208B2 (en) | 2005-05-19 | 2008-03-28 | Laminated tape for packaging materials |
Country Status (4)
Country | Link |
---|---|
JP (2) | JP5106208B2 (en) |
KR (3) | KR100964050B1 (en) |
MY (1) | MY147303A (en) |
TW (1) | TWI332970B (en) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2010116446A (en) * | 2008-11-11 | 2010-05-27 | Tokyo Printing Ink Mfg Co Ltd | Antistatic resin composition and molded product |
JP5577111B2 (en) * | 2010-02-23 | 2014-08-20 | 日東電工株式会社 | Antistatic laminate sheet |
JP2012214252A (en) * | 2010-09-30 | 2012-11-08 | Sumitomo Bakelite Co Ltd | Cover tape for packaging electronic component |
TWI564151B (en) * | 2011-03-30 | 2017-01-01 | 住友電木股份有限公司 | Film and packaged product |
JP5485476B2 (en) * | 2011-07-20 | 2014-05-07 | 三井・デュポンポリケミカル株式会社 | Pressure sensitive adhesive film or sheet, surface protective film or sheet, and method used to protect the surface of an article |
WO2013042727A1 (en) * | 2011-09-22 | 2013-03-28 | 東ソー株式会社 | Adhesive resin composition and easy-peeling film |
JP2016182989A (en) * | 2015-03-27 | 2016-10-20 | 住友ベークライト株式会社 | Electronic component packaging cover tape, electronic component packaging material and electronic component packaging body |
KR101819723B1 (en) * | 2015-12-28 | 2018-03-02 | 주식회사 휴비스 | Environment-Friendly Hot-Melt Adhesive Resin Composition |
CN112352027A (en) * | 2018-06-13 | 2021-02-09 | 琳得科株式会社 | Adhesive sheet |
CN111440556B (en) * | 2019-09-29 | 2022-02-22 | 宁波激智科技股份有限公司 | Protective film and preparation method thereof |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2887359B2 (en) * | 1992-06-04 | 1999-04-26 | 住友ベークライト 株式会社 | Film adhesive |
JPH1017015A (en) * | 1996-06-27 | 1998-01-20 | Nitto Denko Corp | Cover tape for carrier of electronic part |
JP4301673B2 (en) * | 2000-01-19 | 2009-07-22 | 日東電工株式会社 | Laminated tape for packaging materials |
EP1270210B1 (en) * | 2001-06-26 | 2006-08-16 | Sumitomo Bakelite Company Limited | Cover tape for packaging electronic components |
-
2006
- 2006-05-18 KR KR1020060044646A patent/KR100964050B1/en not_active IP Right Cessation
- 2006-05-18 MY MYPI20062285A patent/MY147303A/en unknown
- 2006-05-18 TW TW095117649A patent/TWI332970B/en not_active IP Right Cessation
-
2008
- 2008-03-28 JP JP2008086417A patent/JP5106208B2/en not_active Expired - Fee Related
- 2008-09-02 JP JP2008225174A patent/JP4437505B2/en not_active Expired - Fee Related
-
2009
- 2009-05-18 KR KR1020090043236A patent/KR100964051B1/en not_active IP Right Cessation
-
2010
- 2010-03-25 KR KR1020100026545A patent/KR20100037085A/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
MY147303A (en) | 2012-11-30 |
TW200700520A (en) | 2007-01-01 |
TWI332970B (en) | 2010-11-11 |
KR100964050B1 (en) | 2010-06-16 |
KR100964051B1 (en) | 2010-06-16 |
KR20090055547A (en) | 2009-06-02 |
JP2008285687A (en) | 2008-11-27 |
JP5106208B2 (en) | 2012-12-26 |
KR20100037085A (en) | 2010-04-08 |
KR20060120457A (en) | 2006-11-27 |
JP2008179833A (en) | 2008-08-07 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP4437505B2 (en) | Laminated tape for packaging materials | |
JP6358403B1 (en) | Resin composition, cover tape, and packaging for electronic parts | |
JP6638751B2 (en) | Cover tape and electronic component package | |
JP2016182989A (en) | Electronic component packaging cover tape, electronic component packaging material and electronic component packaging body | |
JP4573442B2 (en) | Bottom cover tape for electronic component carriers | |
WO2005102860A1 (en) | Cover tape, and carrier tape system for packing electronic component | |
JP4301673B2 (en) | Laminated tape for packaging materials | |
JP4198163B2 (en) | Laminated tape for packaging materials | |
JP5419329B2 (en) | Laminated tape for packaging materials | |
JP7018173B2 (en) | Easy-to-peel film | |
CN1865377B (en) | Laminated belt for package material | |
EP1167224B1 (en) | Cover tape for electronic part conveyance and electronic part conveying member | |
KR20030053439A (en) | Cover tape for the electronic part conveyance, process for its production and electronic part conveying member | |
JP2018118766A (en) | Cover tape and packaging body for electronic components | |
JP7206747B2 (en) | Adhesive resin composition and easily peelable film | |
JP2023049018A (en) | Cover tape and electronic component package | |
JP7289816B2 (en) | Cover tape and electronic component package | |
JP2001106994A (en) | Cover tape for electronic component carrier and electronic component carrier | |
JPH09175592A (en) | Cover tape for packing electronic part | |
JP2004237996A (en) | Cover tape and package using the same | |
JP4615984B2 (en) | Cover tape | |
JP5166762B2 (en) | Antistatic film |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20080902 |
|
A871 | Explanation of circumstances concerning accelerated examination |
Free format text: JAPANESE INTERMEDIATE CODE: A871 Effective date: 20090702 |
|
A975 | Report on accelerated examination |
Free format text: JAPANESE INTERMEDIATE CODE: A971005 Effective date: 20090728 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20090929 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20091126 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20091222 |
|
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20091222 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20130115 Year of fee payment: 3 |
|
R150 | Certificate of patent or registration of utility model |
Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20160115 Year of fee payment: 6 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
LAPS | Cancellation because of no payment of annual fees |