WO2011001713A1 - Protection tape for plating - Google Patents
Protection tape for plating Download PDFInfo
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- WO2011001713A1 WO2011001713A1 PCT/JP2010/053779 JP2010053779W WO2011001713A1 WO 2011001713 A1 WO2011001713 A1 WO 2011001713A1 JP 2010053779 W JP2010053779 W JP 2010053779W WO 2011001713 A1 WO2011001713 A1 WO 2011001713A1
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- WIPO (PCT)
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- plating
- sensitive adhesive
- pressure
- protective tape
- photopolymerization initiator
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- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D5/00—Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
- C25D5/02—Electroplating of selected surface areas
- C25D5/022—Electroplating of selected surface areas using masking means
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- 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
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
- C23C18/16—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by reduction or substitution, e.g. electroless plating
- C23C18/1601—Process or apparatus
- C23C18/1603—Process or apparatus coating on selected surface areas
- C23C18/1605—Process or apparatus coating on selected surface areas by masking
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/67—Apparatus specially adapted for handling semiconductor or electric solid state devices during manufacture or treatment thereof; Apparatus specially adapted for handling wafers during manufacture or treatment of semiconductor or electric solid state devices or components ; Apparatus not specifically provided for elsewhere
- H01L21/683—Apparatus specially adapted for handling semiconductor or electric solid state devices during manufacture or treatment thereof; Apparatus specially adapted for handling wafers during manufacture or treatment of semiconductor or electric solid state devices or components ; Apparatus not specifically provided for elsewhere for supporting or gripping
- H01L21/6835—Apparatus specially adapted for handling semiconductor or electric solid state devices during manufacture or treatment thereof; Apparatus specially adapted for handling wafers during manufacture or treatment of semiconductor or electric solid state devices or components ; Apparatus not specifically provided for elsewhere for supporting or gripping using temporarily an auxiliary support
- H01L21/6836—Wafer tapes, e.g. grinding or dicing support tapes
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- 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
- C09J2203/31—Applications of adhesives in processes or use of adhesives in the form of films or foils as a masking tape for painting
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- 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
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2221/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof covered by H01L21/00
- H01L2221/67—Apparatus for handling semiconductor or electric solid state devices during manufacture or treatment thereof; Apparatus for handling wafers during manufacture or treatment of semiconductor or electric solid state devices or components; Apparatus not specifically provided for elsewhere
- H01L2221/683—Apparatus for handling semiconductor or electric solid state devices during manufacture or treatment thereof; Apparatus for handling wafers during manufacture or treatment of semiconductor or electric solid state devices or components; Apparatus not specifically provided for elsewhere for supporting or gripping
- H01L2221/68304—Apparatus for handling semiconductor or electric solid state devices during manufacture or treatment thereof; Apparatus for handling wafers during manufacture or treatment of semiconductor or electric solid state devices or components; Apparatus not specifically provided for elsewhere for supporting or gripping using temporarily an auxiliary support
- H01L2221/68372—Apparatus for handling semiconductor or electric solid state devices during manufacture or treatment thereof; Apparatus for handling wafers during manufacture or treatment of semiconductor or electric solid state devices or components; Apparatus not specifically provided for elsewhere for supporting or gripping using temporarily an auxiliary support used to support a device or wafer when forming electrical connections thereto
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2221/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof covered by H01L21/00
- H01L2221/67—Apparatus for handling semiconductor or electric solid state devices during manufacture or treatment thereof; Apparatus for handling wafers during manufacture or treatment of semiconductor or electric solid state devices or components; Apparatus not specifically provided for elsewhere
- H01L2221/683—Apparatus for handling semiconductor or electric solid state devices during manufacture or treatment thereof; Apparatus for handling wafers during manufacture or treatment of semiconductor or electric solid state devices or components; Apparatus not specifically provided for elsewhere for supporting or gripping
- H01L2221/68304—Apparatus for handling semiconductor or electric solid state devices during manufacture or treatment thereof; Apparatus for handling wafers during manufacture or treatment of semiconductor or electric solid state devices or components; Apparatus not specifically provided for elsewhere for supporting or gripping using temporarily an auxiliary support
- H01L2221/68381—Details of chemical or physical process used for separating the auxiliary support from a device or wafer
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2924/00—Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
- H01L2924/0001—Technical content checked by a classifier
- H01L2924/00013—Fully indexed content
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Metallurgy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- General Physics & Mathematics (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Physics & Mathematics (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- General Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Computer Hardware Design (AREA)
- Mechanical Engineering (AREA)
- Power Engineering (AREA)
- Electrochemistry (AREA)
- Adhesive Tapes (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Chemically Coating (AREA)
- Electroplating Methods And Accessories (AREA)
Abstract
Disclosed is a protection tape for plating, which is capable of preventing occurrence of plating failure and can be easily removed after being used.
Specifically disclosed is a protection tape for plating, which is used for the purpose of protecting a surface that is not to be plated during plating by an electroless plating method or an electrolytic plating method. The protection tape for plating is composed of a base and an adhesive layer that is formed on at least one surface of the base and contains a photocurable adhesive and a photopolymerization initiator. When the molecular weight of the photopolymerization initiator is represented by x and the blending amount of the photopolymerization initiator per 100 parts by weight of the photocurable adhesive in the adhesive layer is represented by y (parts by weight), x and y are within the range indicated by the broken line in fig. 1.
Description
本発明は、使用後は容易に剥離可能であり、かつ、めっき不良の発生を防止できるめっき保護テープに関する。
The present invention relates to a plating protective tape that can be easily peeled off after use and can prevent the occurrence of defective plating.
半導体ウエハの製造においては、アルミニウムパッドと配線ワイヤーとの密着性向上、はんだボールを搭載する際の密着性向上、はんだ拡散防止等の目的で、ウエハの片面にニッケルや金等からなる金属膜（バリアメタル）を形成することが行われる。このようなバリアメタルは、スパッタ等のドライ処理法により形成されていた。
近年、半導体デバイスに対してより高い信頼性が求められるようになってきたことから、バリアメタルを厚くすることが求められるようになってきた。しかし、従来のドライ処理法で厚いバリアメタルを形成するためには、コスト面や作業効率の面で問題があった。そこで、より簡便に厚いバリアメタルを形成可能なウエット処理法が検討されるようになってきた。 In the manufacture of semiconductor wafers, a metal film made of nickel, gold, or the like on one side of the wafer is used for the purpose of improving adhesion between aluminum pads and wiring wires, improving adhesion when mounting solder balls, and preventing solder diffusion. Barrier metal) is formed. Such a barrier metal has been formed by a dry processing method such as sputtering.
In recent years, since higher reliability has been required for semiconductor devices, it has been required to increase the thickness of the barrier metal. However, in order to form a thick barrier metal by the conventional dry processing method, there are problems in terms of cost and work efficiency. Therefore, a wet processing method capable of forming a thick barrier metal more easily has been studied.
近年、半導体デバイスに対してより高い信頼性が求められるようになってきたことから、バリアメタルを厚くすることが求められるようになってきた。しかし、従来のドライ処理法で厚いバリアメタルを形成するためには、コスト面や作業効率の面で問題があった。そこで、より簡便に厚いバリアメタルを形成可能なウエット処理法が検討されるようになってきた。 In the manufacture of semiconductor wafers, a metal film made of nickel, gold, or the like on one side of the wafer is used for the purpose of improving adhesion between aluminum pads and wiring wires, improving adhesion when mounting solder balls, and preventing solder diffusion. Barrier metal) is formed. Such a barrier metal has been formed by a dry processing method such as sputtering.
In recent years, since higher reliability has been required for semiconductor devices, it has been required to increase the thickness of the barrier metal. However, in order to form a thick barrier metal by the conventional dry processing method, there are problems in terms of cost and work efficiency. Therefore, a wet processing method capable of forming a thick barrier metal more easily has been studied.
代表的なウエット処理法としては、無電解めっき法や電解めっき法等のめっき法が挙げられる。めっき法によれば、比較的厚いバリアメタルを容易に形成することができる。しかし、めっき法ではウエハの全体をめっき浴に浸漬する工程が必須となる。この浸漬工程によって、ウエハの他方の面がめっき液で汚染されてしまったり、場合によってはウエハの他方の面にまでめっきが施されてしまうことがあり、歩留まり低下の原因となっていた。
Typical wet treatment methods include plating methods such as electroless plating and electrolytic plating. According to the plating method, a relatively thick barrier metal can be easily formed. However, in the plating method, a step of immersing the entire wafer in a plating bath is essential. Due to this dipping process, the other surface of the wafer may be contaminated with the plating solution, or in some cases, the other surface of the wafer may be plated, causing a decrease in yield.
めっき液との接触を防止したい面を保護する方法としては、レジスト法が提案されている（例えば、特許文献１等）。即ち、めっき工程前に、予めウエハの片面に液状レジストをスピンコート等により被覆し、該レジストを硬化しておくことにより、ウエハの片面を確実に保護することができる。しかし、めっき処理後にレジストを完全に除去するためには、溶剤等を用いた煩雑なレジスト除去工程が必要になるという問題があった。
A resist method has been proposed as a method for protecting the surface to be prevented from contacting with the plating solution (for example, Patent Document 1). That is, by coating a liquid resist on one side of the wafer in advance by spin coating or the like before the plating step and curing the resist, one side of the wafer can be reliably protected. However, in order to completely remove the resist after the plating process, there is a problem that a complicated resist removing process using a solvent or the like is required.
これに対して本発明者は、めっき保護テープによりウエハの片面を保護することを考えた。めっき保護テープを用いれば、面倒な操作を行うことなく、容易にウエハの片面を保護することが期待できる。また、めっき保護テープの粘着剤層として光硬化型粘着剤からなるものを用いることにより、使用後には光を照射して粘着力を低下させることにより、容易に剥離することができる。
しかしながら、光硬化型粘着剤からなる粘着剤層を有するめっき保護テープによりウエハの片面を保護した状態でめっき処理を繰り返し行った場合、充分にめっきされない外観不良のウエハが発生しやすくなることが判ってきた。
本発明は、使用後は容易に剥離可能であり、かつ、めっき不良の発生を防止できるめっき保護テープを提供することを目的とする。 On the other hand, the present inventor considered protecting one side of the wafer with a plating protective tape. If the plating protective tape is used, it can be expected that one side of the wafer is easily protected without troublesome operations. Moreover, by using what consists of a photocurable adhesive as an adhesive layer of a plating protective tape, it can peel easily by irradiating light after use and reducing adhesive force.
However, it has been found that when the plating process is repeated with one side of the wafer protected by a plating protective tape having a pressure-sensitive adhesive layer made of a photocurable pressure-sensitive adhesive, a wafer with poor appearance that is not sufficiently plated is likely to occur. I came.
An object of this invention is to provide the plating protective tape which can be peeled easily after use and can prevent generation | occurrence | production of a plating defect.
しかしながら、光硬化型粘着剤からなる粘着剤層を有するめっき保護テープによりウエハの片面を保護した状態でめっき処理を繰り返し行った場合、充分にめっきされない外観不良のウエハが発生しやすくなることが判ってきた。
本発明は、使用後は容易に剥離可能であり、かつ、めっき不良の発生を防止できるめっき保護テープを提供することを目的とする。 On the other hand, the present inventor considered protecting one side of the wafer with a plating protective tape. If the plating protective tape is used, it can be expected that one side of the wafer is easily protected without troublesome operations. Moreover, by using what consists of a photocurable adhesive as an adhesive layer of a plating protective tape, it can peel easily by irradiating light after use and reducing adhesive force.
However, it has been found that when the plating process is repeated with one side of the wafer protected by a plating protective tape having a pressure-sensitive adhesive layer made of a photocurable pressure-sensitive adhesive, a wafer with poor appearance that is not sufficiently plated is likely to occur. I came.
An object of this invention is to provide the plating protective tape which can be peeled easily after use and can prevent generation | occurrence | production of a plating defect.
本発明１は、無電解めっき法又は電解めっき法によるめっきの際に非めっき面を保護するためのめっき保護テープであって、基材と、前記基材の少なくとも一方の面に形成された光硬化型粘着剤と光重合開始剤とを含有する粘着剤層とからなり、前記光重合開始剤の分子量をｘ、前記粘着剤層中における前記光硬化型粘着剤１００重量部に対する前記光重合開始剤の配合量をｙ重量部としたときに、ｘとｙとが図１の破線で囲まれた範囲内であるめっき保護テープである。
本発明２は、無電解めっき法又は電解めっき法によるめっきの際に非めっき面を保護するためのめっき保護テープであって、基材と、前記基材の少なくとも一方の面に形成された光硬化型粘着剤と光重合開始剤とを含有する粘着剤層とからなり、前記光重合開始剤は、分子末端に水酸基を有するものであるめっき保護テープである。
以下に本発明を詳述する。 The present invention 1 is a plating protective tape for protecting a non-plated surface during plating by an electroless plating method or an electrolytic plating method, and a substrate and light formed on at least one surface of the substrate A pressure-sensitive adhesive layer containing a curable pressure-sensitive adhesive and a photopolymerization initiator, wherein the molecular weight of the photopolymerization initiator is x, and the photopolymerization start with respect to 100 parts by weight of the photo-curable pressure-sensitive adhesive in the pressure-sensitive adhesive layer When the compounding amount of the agent is y parts by weight, it is a plating protective tape in which x and y are within the range surrounded by the broken line in FIG.
The present invention 2 is a plating protective tape for protecting a non-plated surface during plating by an electroless plating method or an electrolytic plating method, and a substrate and light formed on at least one surface of the substrate It consists of a pressure-sensitive adhesive layer containing a curable pressure-sensitive adhesive and a photopolymerization initiator, and the photopolymerization initiator is a plating protective tape having a hydroxyl group at the molecular end.
The present invention is described in detail below.
本発明２は、無電解めっき法又は電解めっき法によるめっきの際に非めっき面を保護するためのめっき保護テープであって、基材と、前記基材の少なくとも一方の面に形成された光硬化型粘着剤と光重合開始剤とを含有する粘着剤層とからなり、前記光重合開始剤は、分子末端に水酸基を有するものであるめっき保護テープである。
以下に本発明を詳述する。 The present invention 1 is a plating protective tape for protecting a non-plated surface during plating by an electroless plating method or an electrolytic plating method, and a substrate and light formed on at least one surface of the substrate A pressure-sensitive adhesive layer containing a curable pressure-sensitive adhesive and a photopolymerization initiator, wherein the molecular weight of the photopolymerization initiator is x, and the photopolymerization start with respect to 100 parts by weight of the photo-curable pressure-sensitive adhesive in the pressure-sensitive adhesive layer When the compounding amount of the agent is y parts by weight, it is a plating protective tape in which x and y are within the range surrounded by the broken line in FIG.
The present invention 2 is a plating protective tape for protecting a non-plated surface during plating by an electroless plating method or an electrolytic plating method, and a substrate and light formed on at least one surface of the substrate It consists of a pressure-sensitive adhesive layer containing a curable pressure-sensitive adhesive and a photopolymerization initiator, and the photopolymerization initiator is a plating protective tape having a hydroxyl group at the molecular end.
The present invention is described in detail below.
本発明者は、めっき処理を繰り返し行ったときに、充分にめっきされない外観不良のウエハが発生する原因を検討した。その結果、めっき保護テープの粘着剤層から溶出する成分によってめっき液が汚染されることに原因があることを見出した。とりわけ、厚さ２００～３００μｍ以下の半導体ウエハのめっきの際の保護にめっき保護テープを用いる場合、薄い半導体ウエハがテープ貼付工程で破損してしまわないように、めっき保護テープを半導体ウエハに比べて大きめに切断する。この状態でめっき液中に浸漬すると、剥きだしの粘着剤層が直接めっき液に曝されることになり、めっき液の汚染が進みやすい。例えば、直径１５０ｍｍの半導体ウエハの片面にめっき処理を施す場合、実生産上では２０～２５枚を１つのウェハカセットに収納した後、カセットごと５０～１００Ｌ程度のめっき液を含むめっき浴を用い、２０００～３０００枚程度の半導体ウエハのめっき処理を行う毎にめっき液の交換を行う。交換前にめっき液の汚染が一定以上に進んでしまった場合に、めっき不良が発生するものと考えられる。
The present inventor has examined the cause of occurrence of a wafer with poor appearance that is not sufficiently plated when the plating process is repeated. As a result, it has been found that there is a cause in that the plating solution is contaminated by components eluted from the adhesive layer of the plating protective tape. In particular, when plating protection tape is used to protect a semiconductor wafer with a thickness of 200 to 300 μm or less, the plating protection tape is compared with that of the semiconductor wafer so that the thin semiconductor wafer will not be damaged in the tape application process. Cut large. When immersed in the plating solution in this state, the exposed adhesive layer is directly exposed to the plating solution, and contamination of the plating solution is likely to proceed. For example, when plating is performed on one side of a semiconductor wafer having a diameter of 150 mm, in actual production, after storing 20 to 25 wafers in one wafer cassette, a plating bath containing about 50 to 100 L of plating solution is used for each cassette. The plating solution is exchanged every time about 2000 to 3000 semiconductor wafers are plated. It is considered that defective plating occurs when the contamination of the plating solution progresses beyond a certain level before replacement.
本発明者は、めっき保護テープの粘着剤層に含まれる成分のうち、光重合開始剤が最もめっき液の汚染を引き起こすことを見出した。
そして、光重合開始剤の分子量と配合量とが特定の範囲内になるように用いることにより、光重合開始剤によるめっき液の汚染を防止し、充分にめっきされない外観不良のウエハの発生を防止できることを見出し、本発明１を完成した。
また、光重合開始剤として特定のものを選択して用いることにより、光重合開始剤によるめっき液の汚染を防止し、充分にめっきされない外観不良のウエハの発生を防止できることを見出し、本発明２を完成した。 This inventor discovered that a photoinitiator caused the contamination of a plating solution most among the components contained in the adhesive layer of a plating protective tape.
By using the photopolymerization initiator so that the molecular weight and blending amount are within a specific range, contamination of the plating solution by the photopolymerization initiator is prevented, and occurrence of wafers with poor appearance that are not sufficiently plated is prevented. As a result, the present invention 1 was completed.
Further, by selecting and using a specific photopolymerization initiator as a photopolymerization initiator, it is found that the plating solution can be prevented from being contaminated by the photopolymerization initiator, and the occurrence of wafers with poor appearance that are not sufficiently plated can be prevented. Was completed.
そして、光重合開始剤の分子量と配合量とが特定の範囲内になるように用いることにより、光重合開始剤によるめっき液の汚染を防止し、充分にめっきされない外観不良のウエハの発生を防止できることを見出し、本発明１を完成した。
また、光重合開始剤として特定のものを選択して用いることにより、光重合開始剤によるめっき液の汚染を防止し、充分にめっきされない外観不良のウエハの発生を防止できることを見出し、本発明２を完成した。 This inventor discovered that a photoinitiator caused the contamination of a plating solution most among the components contained in the adhesive layer of a plating protective tape.
By using the photopolymerization initiator so that the molecular weight and blending amount are within a specific range, contamination of the plating solution by the photopolymerization initiator is prevented, and occurrence of wafers with poor appearance that are not sufficiently plated is prevented. As a result, the present invention 1 was completed.
Further, by selecting and using a specific photopolymerization initiator as a photopolymerization initiator, it is found that the plating solution can be prevented from being contaminated by the photopolymerization initiator, and the occurrence of wafers with poor appearance that are not sufficiently plated can be prevented. Was completed.
本発明１のめっき保護テープは、基材と該基材の少なくとも一方の面に形成された粘着剤層とからなる。
上記基材は特に限定されないが、光を透過又は通過するものであることが好ましく、例えば、アクリル、オレフィン、ポリカーボネート、塩化ビニル、ＡＢＳ、ポリエチレンテレフタレート（ＰＥＴ）、ナイロン、ウレタン、ポリイミド等の透明な樹脂からなるシート、網目状の構造を有するシート、孔が開けられたシート等が挙げられる。 The plating protective tape of the present invention 1 comprises a base material and an adhesive layer formed on at least one surface of the base material.
Although the said base material is not specifically limited, It is preferable that it is what permeate | transmits or passes light, for example, transparent, such as an acryl, an olefin, a polycarbonate, vinyl chloride, ABS, polyethylene terephthalate (PET), nylon, urethane, a polyimide. Examples thereof include a sheet made of resin, a sheet having a network structure, and a sheet having holes.
上記基材は特に限定されないが、光を透過又は通過するものであることが好ましく、例えば、アクリル、オレフィン、ポリカーボネート、塩化ビニル、ＡＢＳ、ポリエチレンテレフタレート（ＰＥＴ）、ナイロン、ウレタン、ポリイミド等の透明な樹脂からなるシート、網目状の構造を有するシート、孔が開けられたシート等が挙げられる。 The plating protective tape of the present invention 1 comprises a base material and an adhesive layer formed on at least one surface of the base material.
Although the said base material is not specifically limited, It is preferable that it is what permeate | transmits or passes light, for example, transparent, such as an acryl, an olefin, a polycarbonate, vinyl chloride, ABS, polyethylene terephthalate (PET), nylon, urethane, a polyimide. Examples thereof include a sheet made of resin, a sheet having a network structure, and a sheet having holes.
上記粘着剤層は、光硬化型粘着剤と光重合開始剤とを含有する。
上記光硬化型粘着剤としては特に限定されず、従来公知のものを用いることができる。具体的には、例えば、分子内にラジカル重合性の不飽和結合を有する（メタ）アクリル酸アルキルエステル系の重合性ポリマーと、ラジカル重合性の多官能オリゴマー又はモノマーとを主成分とし、必要に応じて光重合開始剤を含んでなる光硬化型粘着剤を用いたもの等が挙げられる。
このような光硬化型粘着剤からなる粘着剤層は、光の照射により粘着剤層の全体が均一にかつ速やかに重合架橋して一体化するため、重合硬化による弾性率の上昇が著しくなり、粘着力が大きく低下する。 The pressure-sensitive adhesive layer contains a photocurable pressure-sensitive adhesive and a photopolymerization initiator.
It does not specifically limit as said photocurable adhesive, A conventionally well-known thing can be used. Specifically, for example, a (meth) acrylic acid alkyl ester-based polymerizable polymer having a radical polymerizable unsaturated bond in the molecule and a radical polymerizable polyfunctional oligomer or monomer as main components are necessary. The thing using the photocurable adhesive which contains a photoinitiator according to it, etc. are mentioned.
The pressure-sensitive adhesive layer made of such a photo-curable pressure-sensitive adhesive is uniformly and rapidly polymerized and integrated by light irradiation, so that the elastic modulus increases significantly due to polymerization and curing. Adhesive strength is greatly reduced.
上記光硬化型粘着剤としては特に限定されず、従来公知のものを用いることができる。具体的には、例えば、分子内にラジカル重合性の不飽和結合を有する（メタ）アクリル酸アルキルエステル系の重合性ポリマーと、ラジカル重合性の多官能オリゴマー又はモノマーとを主成分とし、必要に応じて光重合開始剤を含んでなる光硬化型粘着剤を用いたもの等が挙げられる。
このような光硬化型粘着剤からなる粘着剤層は、光の照射により粘着剤層の全体が均一にかつ速やかに重合架橋して一体化するため、重合硬化による弾性率の上昇が著しくなり、粘着力が大きく低下する。 The pressure-sensitive adhesive layer contains a photocurable pressure-sensitive adhesive and a photopolymerization initiator.
It does not specifically limit as said photocurable adhesive, A conventionally well-known thing can be used. Specifically, for example, a (meth) acrylic acid alkyl ester-based polymerizable polymer having a radical polymerizable unsaturated bond in the molecule and a radical polymerizable polyfunctional oligomer or monomer as main components are necessary. The thing using the photocurable adhesive which contains a photoinitiator according to it, etc. are mentioned.
The pressure-sensitive adhesive layer made of such a photo-curable pressure-sensitive adhesive is uniformly and rapidly polymerized and integrated by light irradiation, so that the elastic modulus increases significantly due to polymerization and curing. Adhesive strength is greatly reduced.
上記重合性ポリマーは、例えば、分子内に官能基を持った（メタ）アクリル系ポリマー（以下、官能基含有（メタ）アクリル系ポリマーという）をあらかじめ合成し、分子内に上記の官能基と反応する官能基とラジカル重合性の不飽和結合とを有する化合物（以下、官能基含有不飽和化合物という）と反応させることにより得ることができる。
The polymerizable polymer is prepared by, for example, previously synthesizing a (meth) acrylic polymer having a functional group in the molecule (hereinafter referred to as a functional group-containing (meth) acrylic polymer) and reacting with the functional group in the molecule. It can obtain by making it react with the compound (henceforth a functional group containing unsaturated compound) which has a functional group to perform and a radically polymerizable unsaturated bond.
上記官能基含有（メタ）アクリル系ポリマーは、常温で粘着性を有するポリマーとして、一般の（メタ）アクリル系ポリマーの場合と同様に、アルキル基の炭素数が通常２～１８の範囲にあるアクリル酸アルキルエステル及び／又はメタクリル酸アルキルエステルを主モノマーとし、これと官能基含有モノマーと、更に必要に応じてこれらと共重合可能な他の改質用モノマーとを常法により共重合させることにより得られるものである。上記官能基含有（メタ）アクリル系ポリマーの重量平均分子量は通常２０万～２００万程度である。
The functional group-containing (meth) acrylic polymer is an acrylic polymer having a tackiness at room temperature, as in the case of general (meth) acrylic polymers, in which the alkyl group usually has 2 to 18 carbon atoms. By copolymerizing an acid alkyl ester and / or methacrylic acid alkyl ester as a main monomer, a functional group-containing monomer, and, if necessary, another modifying monomer copolymerizable therewith by a conventional method It is obtained. The weight average molecular weight of the functional group-containing (meth) acrylic polymer is usually about 200,000 to 2,000,000.
上記官能基含有モノマーとしては、例えば、アクリル酸、メタクリル酸等のカルボキシル基含有モノマーや、アクリル酸ヒドロキシエチル、メタクリル酸ヒドロキシエチル等のヒドロキシル基含有モノマーや、アクリル酸グリシジル、メタクリル酸グリシジル等のエポキシ基含有モノマーや、アクリル酸イソシアネートエチル、メタクリル酸イソシアネートエチル等のイソシアネート基含有モノマーや、アクリル酸アミノエチル、メタクリル酸アミノエチル等のアミノ基含有モノマー等が挙げられる。
上記共重合可能な他の改質用モノマーとしては、例えば、酢酸ビニル、アクリロニトリル、スチレン等の一般の（メタ）アクリル系ポリマーに用いられている各種のモノマーが挙げられる。 Examples of the functional group-containing monomer include carboxyl group-containing monomers such as acrylic acid and methacrylic acid, hydroxyl group-containing monomers such as hydroxyethyl acrylate and hydroxyethyl methacrylate, and epoxy such as glycidyl acrylate and glycidyl methacrylate. Examples thereof include group-containing monomers, isocyanate group-containing monomers such as isocyanate ethyl acrylate and isocyanate ethyl methacrylate, and amino group-containing monomers such as aminoethyl acrylate and aminoethyl methacrylate.
Examples of other modifying monomers that can be copolymerized include various monomers used in general (meth) acrylic polymers such as vinyl acetate, acrylonitrile, and styrene.
上記共重合可能な他の改質用モノマーとしては、例えば、酢酸ビニル、アクリロニトリル、スチレン等の一般の（メタ）アクリル系ポリマーに用いられている各種のモノマーが挙げられる。 Examples of the functional group-containing monomer include carboxyl group-containing monomers such as acrylic acid and methacrylic acid, hydroxyl group-containing monomers such as hydroxyethyl acrylate and hydroxyethyl methacrylate, and epoxy such as glycidyl acrylate and glycidyl methacrylate. Examples thereof include group-containing monomers, isocyanate group-containing monomers such as isocyanate ethyl acrylate and isocyanate ethyl methacrylate, and amino group-containing monomers such as aminoethyl acrylate and aminoethyl methacrylate.
Examples of other modifying monomers that can be copolymerized include various monomers used in general (meth) acrylic polymers such as vinyl acetate, acrylonitrile, and styrene.
上記官能基含有（メタ）アクリル系ポリマーに反応させる官能基含有不飽和化合物としては、上記官能基含有（メタ）アクリル系ポリマーの官能基に応じて上述した官能基含有モノマーと同様のものを使用できる。例えば、上記官能基含有（メタ）アクリル系ポリマーの官能基がカルボキシル基の場合はエポキシ基含有モノマーやイソシアネート基含有モノマーが用いられ、同官能基がヒドロキシル基の場合はイソシアネート基含有モノマーが用いられ、同官能基がエポキシ基の場合はカルボキシル基含有モノマーやアクリルアミド等のアミド基含有モノマーが用いられ、同官能基がアミノ基の場合はエポキシ基含有モノマーが用いられる。
The functional group-containing unsaturated compound to be reacted with the functional group-containing (meth) acrylic polymer is the same as the functional group-containing monomer described above according to the functional group of the functional group-containing (meth) acrylic polymer. it can. For example, when the functional group of the functional group-containing (meth) acrylic polymer is a carboxyl group, an epoxy group-containing monomer or an isocyanate group-containing monomer is used, and when the functional group is a hydroxyl group, an isocyanate group-containing monomer is used. When the functional group is an epoxy group, a carboxyl group-containing monomer or an amide group-containing monomer such as acrylamide is used, and when the functional group is an amino group, an epoxy group-containing monomer is used.
上記多官能オリゴマー又はモノマーとしては、分子量が１万以下であるものが好ましく、より好ましくは加熱又は光の照射による粘着剤層の三次元網状化が効率よくなされるように、その分子量が５，０００以下でかつ分子内のラジカル重合性の不飽和結合の数が２～２０個のものである。このようなより好ましい多官能オリゴマー又はモノマーとしては、例えば、トリメチロールプロパントリアクリレート、テトラメチロールメタンテトラアクリレート、ペンタエリスリトールトリアクリレート、ペンタエリスリトールテトラアクリレート、ジペンタエリスリトールモノヒドロキシペンタアクリレート、ジペンタエリスリトールヘキサアクリレート又は上記同様のメタクリレート類等が挙げられる。その他、１，４－ブチレングリコールジアクリレート、１，６－ヘキサンジオールジアクリレート、ポリエチレングリコールジアクリレート、市販のオリゴエステルアクリレート、上記同様のメタクリレート類等が挙げられる。これらの多官能オリゴマー又はモノマーは、単独で用いられてもよく、２種以上が併用されてもよい。
The polyfunctional oligomer or monomer preferably has a molecular weight of 10,000 or less, and more preferably has a molecular weight of 5, so that the three-dimensional network of the pressure-sensitive adhesive layer can be efficiently formed by heating or light irradiation. 000 or less and the number of radically polymerizable unsaturated bonds in the molecule is 2 to 20. Examples of such more preferred polyfunctional oligomers or monomers include trimethylolpropane triacrylate, tetramethylolmethane tetraacrylate, pentaerythritol triacrylate, pentaerythritol tetraacrylate, dipentaerythritol monohydroxypentaacrylate, dipentaerythritol hexaacrylate. Or the above-mentioned methacrylates etc. are mentioned. Other examples include 1,4-butylene glycol diacrylate, 1,6-hexanediol diacrylate, polyethylene glycol diacrylate, commercially available oligoester acrylate, and methacrylates similar to those described above. These polyfunctional oligomers or monomers may be used alone or in combination of two or more.
上記光重合開始剤は、例えば、２５０～８００ｎｍの波長の光を照射することにより活性化されるものが挙げられる。このような光重合開始剤としては、例えば、メトキシアセトフェノン等のアセトフェノン誘導体化合物や、ベンゾインプロピルエーテル、ベンゾインイソブチルエーテル等のベンゾインエーテル系化合物や、ベンジルジメチルケタール、アセトフェノンジエチルケタール等のケタール誘導体化合物や、フォスフィンオキシド誘導体化合物や、ビス（η５－シクロペンタジエニル）チタノセン誘導体化合物、ベンゾフェノン、ミヒラーケトン、クロロチオキサントン、ドデシルチオキサントン、ジメチルチオキサントン、ジエチルチオキサントン、α－ヒドロキシシクロヘキシルフェニルケトン、２－ヒドロキシメチルフェニルプロパン等の光ラジカル重合開始剤が挙げられる。これらの光重合開始剤は、単独で用いられてもよく、２種以上が併用されてもよい。
Examples of the photopolymerization initiator include those that are activated by irradiation with light having a wavelength of 250 to 800 nm. Examples of such a photopolymerization initiator include acetophenone derivative compounds such as methoxyacetophenone, benzoin ether compounds such as benzoin propyl ether and benzoin isobutyl ether, ketal derivative compounds such as benzyldimethyl ketal and acetophenone diethyl ketal, Phosphine oxide derivative compound, bis (η5-cyclopentadienyl) titanocene derivative compound, benzophenone, Michler ketone, chlorothioxanthone, dodecylthioxanthone, dimethylthioxanthone, diethylthioxanthone, α-hydroxycyclohexyl phenyl ketone, 2-hydroxymethylphenylpropane, etc. These radical photopolymerization initiators. These photoinitiators may be used independently and 2 or more types may be used together.
本発明１のめっき保護テープにおいては、光重合開始剤の分子量をｘ、上記粘着剤層中における上記光硬化型粘着剤１００重量部に対する光重合開始剤の配合量をｙ重量部としたときに、ｘとｙとが図１の破線で囲まれた範囲内である。
図１において、光照射により容易にめっき保護テープを剥離でき、かつ、めっき保護テープで片面を保護した直径１５０ｍｍの半導体ウエハを、５０Ｌのめっき液を用いて１０００枚めっき処理したときにめっき不良が発生しない点を「○」で表し、光照射してもめっき保護テープを剥離できないか、又は、めっき保護テープで片面を保護した直径１５０ｍｍの半導体ウエハを、５０Ｌのめっき液を用いて１０００枚めっき処理したときに１枚でもめっき不良が発生する点を「×」でプロットしている。ｘとｙとが図１の破線で囲まれた範囲内である場合に、粘着剤層が直接めっき液に曝されたときに、重合開始剤がめっき液に溶出して汚染するのを防止することができる。また、光を照射したときに、容易にめっき保護テープを剥離することができる。 In the plating protective tape of the present invention 1, when the molecular weight of the photopolymerization initiator is x and the blending amount of the photopolymerization initiator with respect to 100 parts by weight of the photocurable adhesive in the pressure-sensitive adhesive layer is y parts by weight. , X and y are within the range surrounded by the broken line in FIG.
In FIG. 1, the plating protective tape can be easily peeled off by light irradiation, and a plating failure occurs when 1000 sheets of a semiconductor wafer having a diameter of 150 mm whose one side is protected by the plating protective tape is plated using 50 L of plating solution. The point that does not occur is indicated by “◯”, and the plating protective tape cannot be peeled off even when irradiated with light, or a semiconductor wafer having a diameter of 150 mm, which is protected on one side with the plating protective tape, is plated with a 50 L plating solution. The points at which plating defects occur even when one sheet is processed are plotted with “x”. When x and y are within the range surrounded by the broken line in FIG. 1, when the pressure-sensitive adhesive layer is directly exposed to the plating solution, the polymerization initiator is prevented from being eluted into the plating solution and contaminated. be able to. Moreover, the plating protective tape can be easily peeled off when irradiated with light.
図１において、光照射により容易にめっき保護テープを剥離でき、かつ、めっき保護テープで片面を保護した直径１５０ｍｍの半導体ウエハを、５０Ｌのめっき液を用いて１０００枚めっき処理したときにめっき不良が発生しない点を「○」で表し、光照射してもめっき保護テープを剥離できないか、又は、めっき保護テープで片面を保護した直径１５０ｍｍの半導体ウエハを、５０Ｌのめっき液を用いて１０００枚めっき処理したときに１枚でもめっき不良が発生する点を「×」でプロットしている。ｘとｙとが図１の破線で囲まれた範囲内である場合に、粘着剤層が直接めっき液に曝されたときに、重合開始剤がめっき液に溶出して汚染するのを防止することができる。また、光を照射したときに、容易にめっき保護テープを剥離することができる。 In the plating protective tape of the present invention 1, when the molecular weight of the photopolymerization initiator is x and the blending amount of the photopolymerization initiator with respect to 100 parts by weight of the photocurable adhesive in the pressure-sensitive adhesive layer is y parts by weight. , X and y are within the range surrounded by the broken line in FIG.
In FIG. 1, the plating protective tape can be easily peeled off by light irradiation, and a plating failure occurs when 1000 sheets of a semiconductor wafer having a diameter of 150 mm whose one side is protected by the plating protective tape is plated using 50 L of plating solution. The point that does not occur is indicated by “◯”, and the plating protective tape cannot be peeled off even when irradiated with light, or a semiconductor wafer having a diameter of 150 mm, which is protected on one side with the plating protective tape, is plated with a 50 L plating solution. The points at which plating defects occur even when one sheet is processed are plotted with “x”. When x and y are within the range surrounded by the broken line in FIG. 1, when the pressure-sensitive adhesive layer is directly exposed to the plating solution, the polymerization initiator is prevented from being eluted into the plating solution and contaminated. be able to. Moreover, the plating protective tape can be easily peeled off when irradiated with light.
例えば、光重合開始剤の分子量が２５６である場合、上記粘着剤層中における上記光硬化型粘着剤１００重量部に対する光重合開始剤の配合量が０．１～０．３重量部である場合には、光照射により容易にめっき保護テープを剥離でき、かつ、めっき保護テープで片面を保護した直径１５０ｍｍの半導体ウエハを、５０Ｌのめっき液を用いて１０００枚めっき処理してもめっき不良が発生しない。しかしながら、光重合開始剤の配合量が０．０５重量部であると、光を照射しても粘着力が充分に低下せず、めっき保護テープを剥離することができない。光重合開始剤の配合量が０．４重量部であると、めっき保護テープで片面を保護した直径１５０ｍｍの半導体ウエハを、５０Ｌのめっき液を用いて１０００枚めっき処理すると、めっき不良が発生してくる。
For example, when the molecular weight of the photopolymerization initiator is 256, the blending amount of the photopolymerization initiator with respect to 100 parts by weight of the photocurable pressure-sensitive adhesive in the pressure-sensitive adhesive layer is 0.1 to 0.3 parts by weight. The plating protective tape can be easily peeled off by light irradiation, and plating failure occurs even if a semiconductor wafer with a diameter of 150 mm that is protected on one side with a plating protective tape is plated with 1000 sheets of 50 L of plating solution. do not do. However, when the amount of the photopolymerization initiator is 0.05 parts by weight, the adhesive strength is not sufficiently lowered even when irradiated with light, and the plating protective tape cannot be peeled off. When the blending amount of the photopolymerization initiator is 0.4 parts by weight, plating failure occurs when 1000 sheets of a semiconductor wafer having a diameter of 150 mm, which is protected on one side with a plating protective tape, is plated using a 50 L plating solution. Come.
上記光重合開始剤の分子量の好ましい下限は１６２である。上記光重合開始剤の分子量が１６２未満であると、少量の配合であってもめっき液を汚染して、外観不良のウエハの発生の原因となる。
上記光重合開始剤の分子量の上限は特に限定されないが、実質的に数万程度が上限である。上記光重合開始剤の分子量が数万になると、粘着剤層中に溶解できなくなり、その結果、光硬化性を発揮できなくなる。 A preferable lower limit of the molecular weight of the photopolymerization initiator is 162. When the molecular weight of the photopolymerization initiator is less than 162, the plating solution is contaminated even if the amount is small, causing the appearance of a defective wafer.
The upper limit of the molecular weight of the photopolymerization initiator is not particularly limited, but the upper limit is substantially about tens of thousands. When the molecular weight of the photopolymerization initiator reaches tens of thousands, it cannot be dissolved in the pressure-sensitive adhesive layer, and as a result, it cannot exhibit photocurability.
上記光重合開始剤の分子量の上限は特に限定されないが、実質的に数万程度が上限である。上記光重合開始剤の分子量が数万になると、粘着剤層中に溶解できなくなり、その結果、光硬化性を発揮できなくなる。 A preferable lower limit of the molecular weight of the photopolymerization initiator is 162. When the molecular weight of the photopolymerization initiator is less than 162, the plating solution is contaminated even if the amount is small, causing the appearance of a defective wafer.
The upper limit of the molecular weight of the photopolymerization initiator is not particularly limited, but the upper limit is substantially about tens of thousands. When the molecular weight of the photopolymerization initiator reaches tens of thousands, it cannot be dissolved in the pressure-sensitive adhesive layer, and as a result, it cannot exhibit photocurability.
上記粘着剤層は、光を照射することにより気体を発生する気体発生剤を含有してもよい。このような気体発生剤を含有する上記粘着剤層に光を照射すると、上記光硬化性粘着剤が架橋硬化して粘着剤層全体の弾性率が上昇し、このような硬い粘着剤層中で発生した気体は粘着剤層から接着界面に放出され接着面の少なくとも一部を剥離することから、より容易にめっき保護テープを剥離することができる。
The pressure-sensitive adhesive layer may contain a gas generating agent that generates gas when irradiated with light. When the pressure-sensitive adhesive layer containing such a gas generating agent is irradiated with light, the photocurable pressure-sensitive adhesive is cross-linked and cured, and the elastic modulus of the entire pressure-sensitive adhesive layer is increased. In such a hard pressure-sensitive adhesive layer, The generated gas is released from the pressure-sensitive adhesive layer to the bonding interface and peels at least a part of the bonding surface, so that the plating protective tape can be peeled off more easily.
上記気体発生剤は特に限定されないが、例えば、アジド化合物、アゾ化合物等が挙げられる。なかでも、耐熱性に優れるアジド化合物が好適である。
上記アジド化合物としては特に限定されず、例えば、３－アジドメチル－３－メチルオキセタン、テレフタルアジド、ｐ－ｔｅｒｔ－ブチルベンズアジド、３－アジドメチル－３－メチルオキセタンを開環重合することにより得られるグリシジルアジドポリマー（ＧＡＰ）等のアジド基を有するポリマー等が挙げられる。 Although the said gas generating agent is not specifically limited, For example, an azide compound, an azo compound, etc. are mentioned. Of these, an azide compound having excellent heat resistance is preferable.
The azide compound is not particularly limited. For example, glycidyl obtained by ring-opening polymerization of 3-azidomethyl-3-methyloxetane, terephthalazide, p-tert-butylbenzazide, 3-azidomethyl-3-methyloxetane. Examples thereof include a polymer having an azide group such as an azide polymer (GAP).
上記アジド化合物としては特に限定されず、例えば、３－アジドメチル－３－メチルオキセタン、テレフタルアジド、ｐ－ｔｅｒｔ－ブチルベンズアジド、３－アジドメチル－３－メチルオキセタンを開環重合することにより得られるグリシジルアジドポリマー（ＧＡＰ）等のアジド基を有するポリマー等が挙げられる。 Although the said gas generating agent is not specifically limited, For example, an azide compound, an azo compound, etc. are mentioned. Of these, an azide compound having excellent heat resistance is preferable.
The azide compound is not particularly limited. For example, glycidyl obtained by ring-opening polymerization of 3-azidomethyl-3-methyloxetane, terephthalazide, p-tert-butylbenzazide, 3-azidomethyl-3-methyloxetane. Examples thereof include a polymer having an azide group such as an azide polymer (GAP).
上記粘着剤層は、粘着剤としての凝集力の調節を図る目的でイソシアネート化合物、メラミン化合物、エポキシ化合物等の多官能性化合物を含有してもよい。
上記粘着剤層は、必要に応じて、帯電防止剤、可塑剤、樹脂、界面活性剤、ワックス、微粒子充填剤、熱安定剤、酸化防止剤等の公知の添加剤を含有してもよい。 The pressure-sensitive adhesive layer may contain a multifunctional compound such as an isocyanate compound, a melamine compound, or an epoxy compound for the purpose of adjusting the cohesive force as the pressure-sensitive adhesive.
The pressure-sensitive adhesive layer may contain known additives such as an antistatic agent, a plasticizer, a resin, a surfactant, a wax, a fine particle filler, a heat stabilizer, and an antioxidant as necessary.
上記粘着剤層は、必要に応じて、帯電防止剤、可塑剤、樹脂、界面活性剤、ワックス、微粒子充填剤、熱安定剤、酸化防止剤等の公知の添加剤を含有してもよい。 The pressure-sensitive adhesive layer may contain a multifunctional compound such as an isocyanate compound, a melamine compound, or an epoxy compound for the purpose of adjusting the cohesive force as the pressure-sensitive adhesive.
The pressure-sensitive adhesive layer may contain known additives such as an antistatic agent, a plasticizer, a resin, a surfactant, a wax, a fine particle filler, a heat stabilizer, and an antioxidant as necessary.
本発明１のめっき保護テープを製造する方法は特に限定されず、例えば、上記基材上に上記光硬化性粘着剤と光重合開始剤とを含有する粘着剤をドクターナイフやスピンコーター等を用いて塗工する等の従来公知の方法を用いることができる。
The method for producing the plating protective tape of the present invention 1 is not particularly limited. For example, the adhesive containing the photocurable adhesive and the photopolymerization initiator on the substrate is used using a doctor knife or a spin coater. A conventionally known method such as coating may be used.
本発明１のめっき保護テープを用いれば、無電解めっき法又は電解めっき法によるめっきの際に非めっき面を保護する際に、剥きだしの粘着剤層が直接めっき液に曝されてもめっき液を汚染しにくく、めっき不良の発生を効果的に抑制することができる。本発明１のめっき保護テープは、特に無電解めっき法又は電解めっき法により半導体ウエハの片面に厚いバリアメタルを形成する際の、半導体ウエハのめっき液との接触を防止したい面を保護するのに好適に用いることができる。
When the plating protective tape of the present invention 1 is used, the plating solution can be used even when the exposed adhesive layer is directly exposed to the plating solution when protecting the non-plated surface during electroless plating or electrolytic plating. Is difficult to contaminate, and the occurrence of defective plating can be effectively suppressed. The plating protective tape of the present invention 1 protects the surface of the semiconductor wafer that is desired to prevent contact with the plating solution when a thick barrier metal is formed on one surface of the semiconductor wafer, particularly by electroless plating or electrolytic plating. It can be used suitably.
本発明２のめっき保護テープは、基材と該基材の少なくとも一方の面に形成された粘着剤層とからなる。
上記基材は特に限定されないが、光を透過又は通過するものであることが好ましく、例えば、アクリル、オレフィン、ポリカーボネート、塩化ビニル、ＡＢＳ、ポリエチレンテレフタレート（ＰＥＴ）、ナイロン、ウレタン、ポリイミド等の透明な樹脂からなるシート、網目状の構造を有するシート、孔が開けられたシート等が挙げられる。 The plating protective tape of the present invention 2 comprises a base material and an adhesive layer formed on at least one surface of the base material.
Although the said base material is not specifically limited, It is preferable that it is what permeate | transmits or passes light, for example, transparent, such as an acryl, an olefin, a polycarbonate, vinyl chloride, ABS, polyethylene terephthalate (PET), nylon, urethane, a polyimide. Examples thereof include a sheet made of resin, a sheet having a network structure, and a sheet having holes.
上記基材は特に限定されないが、光を透過又は通過するものであることが好ましく、例えば、アクリル、オレフィン、ポリカーボネート、塩化ビニル、ＡＢＳ、ポリエチレンテレフタレート（ＰＥＴ）、ナイロン、ウレタン、ポリイミド等の透明な樹脂からなるシート、網目状の構造を有するシート、孔が開けられたシート等が挙げられる。 The plating protective tape of the present invention 2 comprises a base material and an adhesive layer formed on at least one surface of the base material.
Although the said base material is not specifically limited, It is preferable that it is what permeate | transmits or passes light, for example, transparent, such as an acryl, an olefin, a polycarbonate, vinyl chloride, ABS, polyethylene terephthalate (PET), nylon, urethane, a polyimide. Examples thereof include a sheet made of resin, a sheet having a network structure, and a sheet having holes.
上記粘着剤層は、光硬化型粘着剤と光重合開始剤とを含有する。
上記光硬化型粘着剤としては特に限定されず、従来公知のものを用いることができる。具体的には、例えば、分子内にラジカル重合性の不飽和結合を有する（メタ）アクリル酸アルキルエステル系の重合性ポリマーと、ラジカル重合性の多官能オリゴマー又はモノマーとを主成分とし、必要に応じて光重合開始剤を含んでなる光硬化型粘着剤を用いたもの等が挙げられる。
このような光硬化型粘着剤からなる粘着剤層は、光の照射により粘着剤層の全体が均一にかつ速やかに重合架橋して一体化するため、重合硬化による弾性率の上昇が著しくなり、粘着力が大きく低下する。 The pressure-sensitive adhesive layer contains a photocurable pressure-sensitive adhesive and a photopolymerization initiator.
It does not specifically limit as said photocurable adhesive, A conventionally well-known thing can be used. Specifically, for example, a (meth) acrylic acid alkyl ester-based polymerizable polymer having a radical polymerizable unsaturated bond in the molecule and a radical polymerizable polyfunctional oligomer or monomer as main components are necessary. The thing using the photocurable adhesive which contains a photoinitiator according to it, etc. are mentioned.
The pressure-sensitive adhesive layer made of such a photo-curable pressure-sensitive adhesive is uniformly and rapidly polymerized and integrated by light irradiation, so that the elastic modulus increases significantly due to polymerization and curing. Adhesive strength is greatly reduced.
上記光硬化型粘着剤としては特に限定されず、従来公知のものを用いることができる。具体的には、例えば、分子内にラジカル重合性の不飽和結合を有する（メタ）アクリル酸アルキルエステル系の重合性ポリマーと、ラジカル重合性の多官能オリゴマー又はモノマーとを主成分とし、必要に応じて光重合開始剤を含んでなる光硬化型粘着剤を用いたもの等が挙げられる。
このような光硬化型粘着剤からなる粘着剤層は、光の照射により粘着剤層の全体が均一にかつ速やかに重合架橋して一体化するため、重合硬化による弾性率の上昇が著しくなり、粘着力が大きく低下する。 The pressure-sensitive adhesive layer contains a photocurable pressure-sensitive adhesive and a photopolymerization initiator.
It does not specifically limit as said photocurable adhesive, A conventionally well-known thing can be used. Specifically, for example, a (meth) acrylic acid alkyl ester-based polymerizable polymer having a radical polymerizable unsaturated bond in the molecule and a radical polymerizable polyfunctional oligomer or monomer as main components are necessary. The thing using the photocurable adhesive which contains a photoinitiator according to it, etc. are mentioned.
The pressure-sensitive adhesive layer made of such a photo-curable pressure-sensitive adhesive is uniformly and rapidly polymerized and integrated by light irradiation, so that the elastic modulus increases significantly due to polymerization and curing. Adhesive strength is greatly reduced.
上記重合性ポリマーは、例えば、分子内に官能基を持った（メタ）アクリル系ポリマー（以下、官能基含有（メタ）アクリル系ポリマーという）をあらかじめ合成し、分子内に上記の官能基と反応する官能基とラジカル重合性の不飽和結合とを有する化合物（以下、官能基含有不飽和化合物という）と反応させることにより得ることができる。
The polymerizable polymer is prepared by, for example, previously synthesizing a (meth) acrylic polymer having a functional group in the molecule (hereinafter referred to as a functional group-containing (meth) acrylic polymer) and reacting with the functional group in the molecule. It can obtain by making it react with the compound (henceforth a functional group containing unsaturated compound) which has a functional group to perform and a radically polymerizable unsaturated bond.
上記官能基含有（メタ）アクリル系ポリマーは、常温で粘着性を有するポリマーとして、一般の（メタ）アクリル系ポリマーの場合と同様に、アルキル基の炭素数が通常２～１８の範囲にあるアクリル酸アルキルエステル及び／又はメタクリル酸アルキルエステルを主モノマーとし、これと官能基含有モノマーと、更に必要に応じてこれらと共重合可能な他の改質用モノマーとを常法により共重合させることにより得られるものである。上記官能基含有（メタ）アクリル系ポリマーの重量平均分子量は通常２０万～２００万程度である。
The functional group-containing (meth) acrylic polymer is an acrylic polymer having a tackiness at room temperature, as in the case of general (meth) acrylic polymers, in which the alkyl group usually has 2 to 18 carbon atoms. By copolymerizing an acid alkyl ester and / or methacrylic acid alkyl ester as a main monomer, a functional group-containing monomer, and, if necessary, another modifying monomer copolymerizable therewith by a conventional method It is obtained. The weight average molecular weight of the functional group-containing (meth) acrylic polymer is usually about 200,000 to 2,000,000.
上記官能基含有モノマーとしては、例えば、アクリル酸、メタクリル酸等のカルボキシル基含有モノマーや、アクリル酸ヒドロキシエチル、メタクリル酸ヒドロキシエチル等のヒドロキシル基含有モノマーや、アクリル酸グリシジル、メタクリル酸グリシジル等のエポキシ基含有モノマーや、アクリル酸イソシアネートエチル、メタクリル酸イソシアネートエチル等のイソシアネート基含有モノマーや、アクリル酸アミノエチル、メタクリル酸アミノエチル等のアミノ基含有モノマー等が挙げられる。
上記共重合可能な他の改質用モノマーとしては、例えば、酢酸ビニル、アクリロニトリル、スチレン等の一般の（メタ）アクリル系ポリマーに用いられている各種のモノマーが挙げられる。 Examples of the functional group-containing monomer include carboxyl group-containing monomers such as acrylic acid and methacrylic acid, hydroxyl group-containing monomers such as hydroxyethyl acrylate and hydroxyethyl methacrylate, and epoxy such as glycidyl acrylate and glycidyl methacrylate. Examples thereof include group-containing monomers, isocyanate group-containing monomers such as isocyanate ethyl acrylate and isocyanate ethyl methacrylate, and amino group-containing monomers such as aminoethyl acrylate and aminoethyl methacrylate.
Examples of other modifying monomers that can be copolymerized include various monomers used in general (meth) acrylic polymers such as vinyl acetate, acrylonitrile, and styrene.
上記共重合可能な他の改質用モノマーとしては、例えば、酢酸ビニル、アクリロニトリル、スチレン等の一般の（メタ）アクリル系ポリマーに用いられている各種のモノマーが挙げられる。 Examples of the functional group-containing monomer include carboxyl group-containing monomers such as acrylic acid and methacrylic acid, hydroxyl group-containing monomers such as hydroxyethyl acrylate and hydroxyethyl methacrylate, and epoxy such as glycidyl acrylate and glycidyl methacrylate. Examples thereof include group-containing monomers, isocyanate group-containing monomers such as isocyanate ethyl acrylate and isocyanate ethyl methacrylate, and amino group-containing monomers such as aminoethyl acrylate and aminoethyl methacrylate.
Examples of other modifying monomers that can be copolymerized include various monomers used in general (meth) acrylic polymers such as vinyl acetate, acrylonitrile, and styrene.
上記官能基含有（メタ）アクリル系ポリマーに反応させる官能基含有不飽和化合物としては、上記官能基含有（メタ）アクリル系ポリマーの官能基に応じて上述した官能基含有モノマーと同様のものを使用できる。例えば、上記官能基含有（メタ）アクリル系ポリマーの官能基がカルボキシル基の場合はエポキシ基含有モノマーやイソシアネート基含有モノマーが用いられ、同官能基がヒドロキシル基の場合はイソシアネート基含有モノマーが用いられ、同官能基がエポキシ基の場合はカルボキシル基含有モノマーやアクリルアミド等のアミド基含有モノマーが用いられ、同官能基がアミノ基の場合はエポキシ基含有モノマーが用いられる。
The functional group-containing unsaturated compound to be reacted with the functional group-containing (meth) acrylic polymer is the same as the functional group-containing monomer described above according to the functional group of the functional group-containing (meth) acrylic polymer. it can. For example, when the functional group of the functional group-containing (meth) acrylic polymer is a carboxyl group, an epoxy group-containing monomer or an isocyanate group-containing monomer is used, and when the functional group is a hydroxyl group, an isocyanate group-containing monomer is used. When the functional group is an epoxy group, a carboxyl group-containing monomer or an amide group-containing monomer such as acrylamide is used, and when the functional group is an amino group, an epoxy group-containing monomer is used.
上記多官能オリゴマー又はモノマーとしては、分子量が１万以下であるものが好ましく、より好ましくは加熱又は光の照射による粘着剤層の三次元網状化が効率よくなされるように、その分子量が５，０００以下でかつ分子内のラジカル重合性の不飽和結合の数が２～２０個のものである。このようなより好ましい多官能オリゴマー又はモノマーとしては、例えば、トリメチロールプロパントリアクリレート、テトラメチロールメタンテトラアクリレート、ペンタエリスリトールトリアクリレート、ペンタエリスリトールテトラアクリレート、ジペンタエリスリトールモノヒドロキシペンタアクリレート、ジペンタエリスリトールヘキサアクリレート又は上記同様のメタクリレート類等が挙げられる。その他、１，４－ブチレングリコールジアクリレート、１，６－ヘキサンジオールジアクリレート、ポリエチレングリコールジアクリレート、市販のオリゴエステルアクリレート、上記同様のメタクリレート類等が挙げられる。これらの多官能オリゴマー又はモノマーは、単独で用いられてもよく、２種以上が併用されてもよい。
The polyfunctional oligomer or monomer preferably has a molecular weight of 10,000 or less, and more preferably has a molecular weight of 5, so that the three-dimensional network of the pressure-sensitive adhesive layer can be efficiently formed by heating or light irradiation. 000 or less and the number of radically polymerizable unsaturated bonds in the molecule is 2 to 20. Examples of such more preferred polyfunctional oligomers or monomers include trimethylolpropane triacrylate, tetramethylolmethane tetraacrylate, pentaerythritol triacrylate, pentaerythritol tetraacrylate, dipentaerythritol monohydroxypentaacrylate, dipentaerythritol hexaacrylate. Or the above-mentioned methacrylates etc. are mentioned. Other examples include 1,4-butylene glycol diacrylate, 1,6-hexanediol diacrylate, polyethylene glycol diacrylate, commercially available oligoester acrylate, and methacrylates similar to those described above. These polyfunctional oligomers or monomers may be used alone or in combination of two or more.
上記光重合開始剤は、例えば、２５０～５００ｎｍの波長の光を照射することにより活性化されるものが挙げられる。このような光重合開始剤としては、例えば、メトキシアセトフェノン等のアセトフェノン誘導体化合物や、ベンゾインプロピルエーテル、ベンゾインイソブチルエーテル等のベンゾインエーテル系化合物や、ベンジルジメチルケタール、アセトフェノンジエチルケタール等のケタール誘導体化合物や、フォスフィンオキシド誘導体化合物や、ビス（η５－シクロペンタジエニル）チタノセン誘導体化合物、ベンゾフェノン、ミヒラーケトン、クロロチオキサントン、ドデシルチオキサントン、ジメチルチオキサントン、ジエチルチオキサントン、α－ヒドロキシシクロヘキシルフェニルケトン、２－ヒドロキシメチルフェニルプロパン等の光ラジカル重合開始剤が挙げられる。
Examples of the photopolymerization initiator include those that are activated by irradiation with light having a wavelength of 250 to 500 nm. Examples of such a photopolymerization initiator include acetophenone derivative compounds such as methoxyacetophenone, benzoin ether compounds such as benzoin propyl ether and benzoin isobutyl ether, ketal derivative compounds such as benzyldimethyl ketal and acetophenone diethyl ketal, Phosphine oxide derivative compound, bis (η5-cyclopentadienyl) titanocene derivative compound, benzophenone, Michler ketone, chlorothioxanthone, dodecylthioxanthone, dimethylthioxanthone, diethylthioxanthone, α-hydroxycyclohexyl phenyl ketone, 2-hydroxymethylphenylpropane, etc. These radical photopolymerization initiators.
本発明２においては、これらの光重合開始剤のなかでも、分子末端に水酸基を有する光重合開始剤を選択して用いる。上記重合開始剤が分子末端に水酸基を有することにより、粘着剤層が直接めっき液に曝されたときに、重合開始剤がめっき液に溶出するのを防止することができる。
上記光硬化型粘着剤と重合開始剤とを含有する粘着剤層を形成する際には、粘着剤としての凝集力の調節を図る目的でイソシアネート化合物、メラミン化合物、エポキシ化合物等の多官能性化合物が配合される。このときイソシアネート化合物等と上記重合開始剤の分子末端の水酸基とが反応して、上記重合開始剤が粘着剤層中に化学的に結合して取り込まれる。このため、重合開始剤の溶出が抑制されるものと考えられる。 In the present invention 2, among these photopolymerization initiators, a photopolymerization initiator having a hydroxyl group at the molecular end is selected and used. When the polymerization initiator has a hydroxyl group at the molecular end, it is possible to prevent the polymerization initiator from eluting into the plating solution when the pressure-sensitive adhesive layer is directly exposed to the plating solution.
When forming a pressure-sensitive adhesive layer containing the photocurable pressure-sensitive adhesive and a polymerization initiator, a polyfunctional compound such as an isocyanate compound, a melamine compound, or an epoxy compound is used for the purpose of adjusting the cohesive force as the pressure-sensitive adhesive. Is blended. At this time, the isocyanate compound or the like reacts with the hydroxyl group at the molecular end of the polymerization initiator, and the polymerization initiator is chemically bonded and incorporated into the pressure-sensitive adhesive layer. For this reason, it is thought that elution of a polymerization initiator is suppressed.
上記光硬化型粘着剤と重合開始剤とを含有する粘着剤層を形成する際には、粘着剤としての凝集力の調節を図る目的でイソシアネート化合物、メラミン化合物、エポキシ化合物等の多官能性化合物が配合される。このときイソシアネート化合物等と上記重合開始剤の分子末端の水酸基とが反応して、上記重合開始剤が粘着剤層中に化学的に結合して取り込まれる。このため、重合開始剤の溶出が抑制されるものと考えられる。 In the present invention 2, among these photopolymerization initiators, a photopolymerization initiator having a hydroxyl group at the molecular end is selected and used. When the polymerization initiator has a hydroxyl group at the molecular end, it is possible to prevent the polymerization initiator from eluting into the plating solution when the pressure-sensitive adhesive layer is directly exposed to the plating solution.
When forming a pressure-sensitive adhesive layer containing the photocurable pressure-sensitive adhesive and a polymerization initiator, a polyfunctional compound such as an isocyanate compound, a melamine compound, or an epoxy compound is used for the purpose of adjusting the cohesive force as the pressure-sensitive adhesive. Is blended. At this time, the isocyanate compound or the like reacts with the hydroxyl group at the molecular end of the polymerization initiator, and the polymerization initiator is chemically bonded and incorporated into the pressure-sensitive adhesive layer. For this reason, it is thought that elution of a polymerization initiator is suppressed.
上記分子末端に水酸基を有する光重合開始剤は、例えば、１－ヒドロキシ－シクロヘキシル－フェニル－ケトン、２－ヒドロキシ－２－メチル－１－フェニル－プロパン－１－オン、１－〔４－（２－ヒドロキシエトキシ）－フェニル〕－２－ヒドロキシ－２－メチル－１－プロパン－１－オン、２－ヒドロキシ－１－｛４－〔４－（２－ヒドロキシ－２－メチル－プロピオニル）－ベンジル〕－フェニル｝－２－メチル－プロパン－１－オン、オリゴ｛２－ヒドロキシ－２－メチル－１－〔４－（１－メチルビニル）フェニル〕プロパン－オン｝等が挙げられる。
上記分子末端に水酸基を有する光重合開始剤のうち市販されているもの、例えば、エサキュアワン（ランベルティ社製）、イルガキュア１８４、ダロキュア１１７３、イルガキュア２９５９、イルガキュア１２７（以上、チバ・スペシャルティ・ケミカルズ社製）等が挙げられる。 Examples of the photopolymerization initiator having a hydroxyl group at the molecular end include 1-hydroxy-cyclohexyl-phenyl-ketone, 2-hydroxy-2-methyl-1-phenyl-propan-1-one, 1- [4- (2 -Hydroxyethoxy) -phenyl] -2-hydroxy-2-methyl-1-propan-1-one, 2-hydroxy-1- {4- [4- (2-hydroxy-2-methyl-propionyl) -benzyl] -Phenyl} -2-methyl-propan-1-one, oligo {2-hydroxy-2-methyl-1- [4- (1-methylvinyl) phenyl] propan-one} and the like.
Of the above photopolymerization initiators having a hydroxyl group at the molecular terminal, commercially available ones such as Esacure One (Lamberti), Irgacure 184, Darocur 1173, Irgacure 2959, Irgacure 127 (above, Ciba Specialty Chemicals) ) And the like.
上記分子末端に水酸基を有する光重合開始剤のうち市販されているもの、例えば、エサキュアワン（ランベルティ社製）、イルガキュア１８４、ダロキュア１１７３、イルガキュア２９５９、イルガキュア１２７（以上、チバ・スペシャルティ・ケミカルズ社製）等が挙げられる。 Examples of the photopolymerization initiator having a hydroxyl group at the molecular end include 1-hydroxy-cyclohexyl-phenyl-ketone, 2-hydroxy-2-methyl-1-phenyl-propan-1-one, 1- [4- (2 -Hydroxyethoxy) -phenyl] -2-hydroxy-2-methyl-1-propan-1-one, 2-hydroxy-1- {4- [4- (2-hydroxy-2-methyl-propionyl) -benzyl] -Phenyl} -2-methyl-propan-1-one, oligo {2-hydroxy-2-methyl-1- [4- (1-methylvinyl) phenyl] propan-one} and the like.
Of the above photopolymerization initiators having a hydroxyl group at the molecular terminal, commercially available ones such as Esacure One (Lamberti), Irgacure 184, Darocur 1173, Irgacure 2959, Irgacure 127 (above, Ciba Specialty Chemicals) ) And the like.
上記粘着剤層における上記光重合開始剤の配合量は特に限定されず、上記光硬化性粘着剤１００重量部に対して好ましい下限は０．１重量部、好ましい上限は５重量部である。上記光重合開始剤の配合量が０．１重量部未満であると、光照射しても充分に硬化せず、剥離しにくくなることがあり、５重量部を超えると、めっき液を汚染しやすくなることがある。上記光重合開始剤の配合量のより好ましい上限は２重量部である。
The compounding quantity of the said photoinitiator in the said adhesive layer is not specifically limited, A preferable minimum is 0.1 weight part with respect to 100 weight part of said photocurable adhesives, and a preferable upper limit is 5 weight part. If the blending amount of the photopolymerization initiator is less than 0.1 parts by weight, it may not be sufficiently cured even when irradiated with light, and may be difficult to peel. If it exceeds 5 parts by weight, the plating solution may be contaminated. May be easier. A more preferable upper limit of the amount of the photopolymerization initiator is 2 parts by weight.
上記粘着剤層は、光を照射することにより気体を発生する気体発生剤を含有してもよい。このような気体発生剤を含有する上記粘着剤層に光を照射すると、上記光硬化性粘着剤が架橋硬化して粘着剤層全体の弾性率が上昇し、このような硬い粘着剤層中で発生した気体は粘着剤層から接着界面に放出され接着面の少なくとも一部を剥離することから、より容易にめっき保護テープを剥離することができる。
The pressure-sensitive adhesive layer may contain a gas generating agent that generates gas when irradiated with light. When the pressure-sensitive adhesive layer containing such a gas generating agent is irradiated with light, the photocurable pressure-sensitive adhesive is cross-linked and cured, and the elastic modulus of the entire pressure-sensitive adhesive layer is increased. In such a hard pressure-sensitive adhesive layer, The generated gas is released from the pressure-sensitive adhesive layer to the bonding interface and peels at least a part of the bonding surface, so that the plating protective tape can be peeled off more easily.
上記気体発生剤は特に限定されないが、例えば、アジド化合物、アゾ化合物等が挙げられる。なかでも、耐熱性に優れるアジド化合物が好適である。
上記アジド化合物としては特に限定されず、例えば、３－アジドメチル－３－メチルオキセタン、テレフタルアジド、ｐ－ｔｅｒｔ－ブチルベンズアジド、３－アジドメチル－３－メチルオキセタンを開環重合することにより得られるグリシジルアジドポリマー（ＧＡＰ）等のアジド基を有するポリマー等が挙げられる。 Although the said gas generating agent is not specifically limited, For example, an azide compound, an azo compound, etc. are mentioned. Of these, an azide compound having excellent heat resistance is preferable.
The azide compound is not particularly limited. For example, glycidyl obtained by ring-opening polymerization of 3-azidomethyl-3-methyloxetane, terephthalazide, p-tert-butylbenzazide, 3-azidomethyl-3-methyloxetane. Examples thereof include a polymer having an azide group such as an azide polymer (GAP).
上記アジド化合物としては特に限定されず、例えば、３－アジドメチル－３－メチルオキセタン、テレフタルアジド、ｐ－ｔｅｒｔ－ブチルベンズアジド、３－アジドメチル－３－メチルオキセタンを開環重合することにより得られるグリシジルアジドポリマー（ＧＡＰ）等のアジド基を有するポリマー等が挙げられる。 Although the said gas generating agent is not specifically limited, For example, an azide compound, an azo compound, etc. are mentioned. Of these, an azide compound having excellent heat resistance is preferable.
The azide compound is not particularly limited. For example, glycidyl obtained by ring-opening polymerization of 3-azidomethyl-3-methyloxetane, terephthalazide, p-tert-butylbenzazide, 3-azidomethyl-3-methyloxetane. Examples thereof include a polymer having an azide group such as an azide polymer (GAP).
上記粘着剤層は、必要に応じて、帯電防止剤、可塑剤、樹脂、界面活性剤、ワックス、微粒子充填剤、熱安定剤、酸化防止剤等の公知の添加剤を含有してもよい。
The pressure-sensitive adhesive layer may contain known additives such as an antistatic agent, a plasticizer, a resin, a surfactant, a wax, a fine particle filler, a heat stabilizer, and an antioxidant as necessary.
本発明２のめっき保護テープを製造する方法は特に限定されず、例えば、上記基材上に上記光硬化性粘着剤と光重合開始剤とを含有する粘着剤をドクターナイフやスピンコーター等を用いて塗工する等の従来公知の方法を用いることができる。
The method for producing the plating protective tape of the present invention 2 is not particularly limited. For example, the adhesive containing the photocurable adhesive and the photopolymerization initiator on the substrate is used using a doctor knife or a spin coater. A conventionally known method such as coating may be used.
本発明のめっき保護テープを用いれば、無電解めっき法又は電解めっき法によるめっきの時に非めっき面を保護する際に、剥きだしの粘着剤層が直接めっき液に曝されてもめっき液を汚染しにくく、めっき不良の発生を効果的に抑制することができる。本発明２のめっき保護テープは、特に無電解めっき法又は電解めっき法により半導体ウエハの片面に厚いバリアメタルを形成する際の、半導体ウエハのめっき液との接触を防止したい面を保護するのに好適に用いることができる。
When the plating protective tape of the present invention is used, the plating solution is contaminated even when the exposed adhesive layer is directly exposed to the plating solution when protecting the non-plated surface during plating by the electroless plating method or the electrolytic plating method. And the occurrence of defective plating can be effectively suppressed. The plating protective tape of the present invention 2 protects the surface of the semiconductor wafer that is desired to prevent contact with the plating solution when a thick barrier metal is formed on one surface of the semiconductor wafer, particularly by electroless plating or electrolytic plating. It can be used suitably.
本発明によれば、使用後は容易に剥離可能であり、かつ、めっき不良の発生を防止できるめっき保護テープを提供することができる。
ADVANTAGE OF THE INVENTION According to this invention, the plating protective tape which can be peeled easily after use and can prevent generation | occurrence | production of a plating defect can be provided.
以下に実施例を挙げて本発明の態様を更に詳しく説明するが、本発明はこれら実施例にのみ限定されるものではない。
Hereinafter, embodiments of the present invention will be described in more detail with reference to examples. However, the present invention is not limited to these examples.
（実験例）
（１）光硬化型粘着剤の調製
下記の化合物を酢酸エチルに溶解させ、紫外線を照射して重合を行い、重量平均分子量５０万の共重合体からなる光硬化性粘着剤の酢酸エチル溶液を得た。
エチルアクリレート ７５重量部
メチルメタクリレート ２０重量部
アクリル酸 ３重量部
２－ヒドロキシエチルアクリレート ２重量部
光重合開始剤 １重量部
（イルガキュア６５１、５０％酢酸エチル溶液）
ラウリルメルカプタン ０．０１重量部 (Experimental example)
(1) Preparation of photocurable pressure-sensitive adhesive The following compounds are dissolved in ethyl acetate, polymerized by irradiating ultraviolet rays, and an ethyl acetate solution of a photocurable pressure-sensitive adhesive made of a copolymer having a weight average molecular weight of 500,000 is prepared. Obtained.
Ethyl acrylate 75 parts by weight Methyl methacrylate 20 parts by weight Acrylic acid 3 parts by weight 2-hydroxyethyl acrylate 2 parts by weight Photopolymerization initiator 1 part by weight (Irgacure 651, 50% ethyl acetate solution)
Lauryl mercaptan 0.01 parts by weight
（１）光硬化型粘着剤の調製
下記の化合物を酢酸エチルに溶解させ、紫外線を照射して重合を行い、重量平均分子量５０万の共重合体からなる光硬化性粘着剤の酢酸エチル溶液を得た。
エチルアクリレート ７５重量部
メチルメタクリレート ２０重量部
アクリル酸 ３重量部
２－ヒドロキシエチルアクリレート ２重量部
光重合開始剤 １重量部
（イルガキュア６５１、５０％酢酸エチル溶液）
ラウリルメルカプタン ０．０１重量部 (Experimental example)
(1) Preparation of photocurable pressure-sensitive adhesive The following compounds are dissolved in ethyl acetate, polymerized by irradiating ultraviolet rays, and an ethyl acetate solution of a photocurable pressure-sensitive adhesive made of a copolymer having a weight average molecular weight of 500,000 is prepared. Obtained.
Ethyl acrylate 75 parts by weight Methyl methacrylate 20 parts by weight Acrylic acid 3 parts by weight 2-hydroxyethyl acrylate 2 parts by weight Photopolymerization initiator 1 part by weight (Irgacure 651, 50% ethyl acetate solution)
Lauryl mercaptan 0.01 parts by weight
（２）粘着剤層用組成物溶液の調製
得られた光硬化性粘着剤の酢酸エチル溶液の樹脂固形分１００重量部に対して、２－イソシアナトエチルメタクリレート３．５重量部を加えて反応させ、更に、反応後の酢酸エチル溶液の樹脂固形分１００重量部に対して、光重合開始剤としてオリゴ｛２－ヒドロキシ－２－メチル－１－〔４－（１－メチルビニル）フェニル〕プロパン－オン｝（ランベルティ社製、エサキュアワン、分子量４３８）２重量部、ポリイソシアネート０．５重量部を混合し粘着剤層用組成物溶液を調製した。 (2) Preparation of composition solution for pressure-sensitive adhesive layer The reaction was conducted by adding 3.5 parts by weight of 2-isocyanatoethyl methacrylate to 100 parts by weight of the resin solid content of the obtained photocurable pressure-sensitive adhesive in ethyl acetate. Furthermore, oligo {2-hydroxy-2-methyl-1- [4- (1-methylvinyl) phenyl] propane is used as a photopolymerization initiator for 100 parts by weight of the resin solid content of the ethyl acetate solution after the reaction. -ON} (Lamberti, Esacureone, molecular weight 438) 2 parts by weight and polyisocyanate 0.5 part by weight were mixed to prepare an adhesive layer composition solution.
得られた光硬化性粘着剤の酢酸エチル溶液の樹脂固形分１００重量部に対して、２－イソシアナトエチルメタクリレート３．５重量部を加えて反応させ、更に、反応後の酢酸エチル溶液の樹脂固形分１００重量部に対して、光重合開始剤としてオリゴ｛２－ヒドロキシ－２－メチル－１－〔４－（１－メチルビニル）フェニル〕プロパン－オン｝（ランベルティ社製、エサキュアワン、分子量４３８）２重量部、ポリイソシアネート０．５重量部を混合し粘着剤層用組成物溶液を調製した。 (2) Preparation of composition solution for pressure-sensitive adhesive layer The reaction was conducted by adding 3.5 parts by weight of 2-isocyanatoethyl methacrylate to 100 parts by weight of the resin solid content of the obtained photocurable pressure-sensitive adhesive in ethyl acetate. Furthermore, oligo {2-hydroxy-2-methyl-1- [4- (1-methylvinyl) phenyl] propane is used as a photopolymerization initiator for 100 parts by weight of the resin solid content of the ethyl acetate solution after the reaction. -ON} (Lamberti, Esacureone, molecular weight 438) 2 parts by weight and polyisocyanate 0.5 part by weight were mixed to prepare an adhesive layer composition solution.
（３）めっき保護テープの製造
得られた粘着剤層用組成物溶液を、片面にコロナ処理を施した厚さ７５μｍの透明なポリエチレンテレフタレート（ＰＥＴ）フィルムのコロナ処理上に乾燥皮膜の厚さが約１５μｍとなるようにドクターナイフで塗工し１１０℃、５分間加熱して塗工溶液を乾燥させた。乾燥後の粘着剤層は乾燥状態で粘着性を示した。次いで、粘着剤層の表面に離型処理が施されたＰＥＴフィルムを貼り付けた。その後、４０℃、３日間静置養生を行い、めっき保護テープを得た。 (3) Manufacture of plating protective tape The composition solution for the pressure-sensitive adhesive layer obtained was subjected to corona treatment on a transparent polyethylene terephthalate (PET) film having a thickness of 75 μm and subjected to corona treatment on one side. The coating solution was dried with a doctor knife so as to be about 15 μm and heated at 110 ° C. for 5 minutes. The pressure-sensitive adhesive layer after drying showed adhesiveness in a dry state. Next, a PET film that was subjected to a release treatment was attached to the surface of the pressure-sensitive adhesive layer. Then, stationary curing was performed at 40 ° C. for 3 days to obtain a plating protective tape.
得られた粘着剤層用組成物溶液を、片面にコロナ処理を施した厚さ７５μｍの透明なポリエチレンテレフタレート（ＰＥＴ）フィルムのコロナ処理上に乾燥皮膜の厚さが約１５μｍとなるようにドクターナイフで塗工し１１０℃、５分間加熱して塗工溶液を乾燥させた。乾燥後の粘着剤層は乾燥状態で粘着性を示した。次いで、粘着剤層の表面に離型処理が施されたＰＥＴフィルムを貼り付けた。その後、４０℃、３日間静置養生を行い、めっき保護テープを得た。 (3) Manufacture of plating protective tape The composition solution for the pressure-sensitive adhesive layer obtained was subjected to corona treatment on a transparent polyethylene terephthalate (PET) film having a thickness of 75 μm and subjected to corona treatment on one side. The coating solution was dried with a doctor knife so as to be about 15 μm and heated at 110 ° C. for 5 minutes. The pressure-sensitive adhesive layer after drying showed adhesiveness in a dry state. Next, a PET film that was subjected to a release treatment was attached to the surface of the pressure-sensitive adhesive layer. Then, stationary curing was performed at 40 ° C. for 3 days to obtain a plating protective tape.
（４）その他のめっき保護テープの製造
光重合開始剤の種類と配合量とを表１に示したようにした以外は同様の方法により、光重合開始剤の分子量と配合量とが異なるめっき保護テープを製造した。
なお、光重合開始剤は以下の市販品を用いた。 (4) Manufacture of other plating protective tapes The plating protection in which the molecular weight and the blending amount of the photopolymerization initiator are different by the same method except that the types and blending amounts of the photopolymerization initiator are shown in Table 1. Tape was manufactured.
The following commercially available products were used as the photopolymerization initiator.
光重合開始剤の種類と配合量とを表１に示したようにした以外は同様の方法により、光重合開始剤の分子量と配合量とが異なるめっき保護テープを製造した。
なお、光重合開始剤は以下の市販品を用いた。 (4) Manufacture of other plating protective tapes The plating protection in which the molecular weight and the blending amount of the photopolymerization initiator are different by the same method except that the types and blending amounts of the photopolymerization initiator are shown in Table 1. Tape was manufactured.
The following commercially available products were used as the photopolymerization initiator.
フェニルグリオキシリックアジッドメチルエステル（チバ・スペシャルティ・ケミカルズ社製、ダロキュアＭＢＦ、分子量１６２）
２，２－ジメトキシ－１，２－ジフェニル－１－オン（チバ・スペシャルティ・ケミカルズ社製、イルガキュア６５１、分子量２５６）
２－ベンジル－２－ジメチルアミノ－１－（４－モルフォリノフェニル）－ブタノン－１（チバ・スペシャルティ・ケミカルズ社製、イルガキュア３６９、分子量３６６）
オリゴ｛２－ヒドロキシ－２－メチル－１－〔４－（１－メチルビニル）フェニル〕プロパン－オン｝（ランベルティ社製、エサキュアＫＩＰ１５０、分子量６５７） Phenylglyoxylic azide methyl ester (Ciba Specialty Chemicals, Darocur MBF, molecular weight 162)
2,2-dimethoxy-1,2-diphenyl-1-one (manufactured by Ciba Specialty Chemicals, Irgacure 651, molecular weight 256)
2-Benzyl-2-dimethylamino-1- (4-morpholinophenyl) -butanone-1 (manufactured by Ciba Specialty Chemicals, Irgacure 369, molecular weight 366)
Oligo {2-hydroxy-2-methyl-1- [4- (1-methylvinyl) phenyl] propan-one} (Lamberti, Esacure KIP150, molecular weight 657)
２，２－ジメトキシ－１，２－ジフェニル－１－オン（チバ・スペシャルティ・ケミカルズ社製、イルガキュア６５１、分子量２５６）
２－ベンジル－２－ジメチルアミノ－１－（４－モルフォリノフェニル）－ブタノン－１（チバ・スペシャルティ・ケミカルズ社製、イルガキュア３６９、分子量３６６）
オリゴ｛２－ヒドロキシ－２－メチル－１－〔４－（１－メチルビニル）フェニル〕プロパン－オン｝（ランベルティ社製、エサキュアＫＩＰ１５０、分子量６５７） Phenylglyoxylic azide methyl ester (Ciba Specialty Chemicals, Darocur MBF, molecular weight 162)
2,2-dimethoxy-1,2-diphenyl-1-one (manufactured by Ciba Specialty Chemicals, Irgacure 651, molecular weight 256)
2-Benzyl-2-dimethylamino-1- (4-morpholinophenyl) -butanone-1 (manufactured by Ciba Specialty Chemicals, Irgacure 369, molecular weight 366)
Oligo {2-hydroxy-2-methyl-1- [4- (1-methylvinyl) phenyl] propan-one} (Lamberti, Esacure KIP150, molecular weight 657)
（評価）
得られためっき保護テープについて、以下の方法により評価を行った。 (Evaluation)
The obtained plating protective tape was evaluated by the following method.
得られためっき保護テープについて、以下の方法により評価を行った。 (Evaluation)
The obtained plating protective tape was evaluated by the following method.
厚さ２００μｍ、直径１５０ｍｍのＳｉウエハの片面に、得られためっき保護テープを貼り合わせた後、２３℃で２０分静置した。その後、ウエハの外周に沿って、めっき保護テープのはみ出し量が０．５ｍｍとなるようにめっき保護テープを切断した。なお、めっき保護テープのはみ出し量を０．５ｍｍ未満としようとすると、ウエハが破損してしまうことがあった。
The obtained plating protective tape was bonded to one side of a Si wafer having a thickness of 200 μm and a diameter of 150 mm, and then allowed to stand at 23 ° C. for 20 minutes. Thereafter, the plating protective tape was cut along the outer periphery of the wafer so that the protruding amount of the plating protective tape was 0.5 mm. If the amount of protrusion of the plating protective tape is less than 0.5 mm, the wafer may be damaged.
めっき保護テープにより保護されたウエハのめっきを施す面に、メルクリーナーＳＣ－７００１（メルテックス株式会社製）を用いて脱脂処理し、メルプレートＥ－７１２１（メルテックス株式会社製）を用いてエッチング処理を行った後、メルプレートコンディショナー７２３０（メルテックス株式会社製）を用いてコンディショニングを行った。次いで、メルプレートＦＺ－７３５０（メルテックス株式会社製）を用いて第１亜鉛置換処理を行い、３０ｗｔ％の硝酸を用いた亜鉛剥離を行い、メルプレートＦＢＺ（メルテックス株式会社製）を用いて第２亜鉛置換処理を行った。次いで、無電解ニッケルめっき液（メルプレートＮＩ－８６９、メルテックス株式会社製）を用いた無電解ニッケルめっきと、無電解金めっき液（メルプレートＡｕ－７６２１、メルテックス株式会社製）を用いた無電解金めっきを行い、めっき工程を完了した。
めっき工程後、めっき保護テープの基材側から２０００ｍＪ／ｃｍ２の紫外線を照射して、めっき保護テープを剥離した。このとき、剥離できなかった場合は「×」と評価した。 The surface to be plated of the wafer protected by the plating protective tape is degreased using Mel Cleaner SC-7001 (Meltex Co., Ltd.) and etched using Mel Plate E-7121 (Meltex Co., Ltd.). After the treatment, conditioning was performed using Melplate Conditioner 7230 (Meltex Co., Ltd.). Next, a first zinc replacement treatment was performed using Melplate FZ-7350 (Meltex Co., Ltd.), zinc peeling using 30 wt% nitric acid was performed, and Melplate FBZ (Meltex Co., Ltd.) was used. A second zinc replacement treatment was performed. Next, electroless nickel plating using an electroless nickel plating solution (Melplate NI-869, manufactured by Meltex Co., Ltd.) and an electroless gold plating solution (Melplate Au-7621, manufactured by Meltex Co., Ltd.) were used. Electroless gold plating was performed to complete the plating process.
After the plating step, the plating protective tape was peeled off by irradiating with 2000 mJ / cm 2 ultraviolet rays from the substrate side of the plating protective tape. At this time, when it was not able to peel, it evaluated as "x".
めっき工程後、めっき保護テープの基材側から２０００ｍＪ／ｃｍ２の紫外線を照射して、めっき保護テープを剥離した。このとき、剥離できなかった場合は「×」と評価した。 The surface to be plated of the wafer protected by the plating protective tape is degreased using Mel Cleaner SC-7001 (Meltex Co., Ltd.) and etched using Mel Plate E-7121 (Meltex Co., Ltd.). After the treatment, conditioning was performed using Melplate Conditioner 7230 (Meltex Co., Ltd.). Next, a first zinc replacement treatment was performed using Melplate FZ-7350 (Meltex Co., Ltd.), zinc peeling using 30 wt% nitric acid was performed, and Melplate FBZ (Meltex Co., Ltd.) was used. A second zinc replacement treatment was performed. Next, electroless nickel plating using an electroless nickel plating solution (Melplate NI-869, manufactured by Meltex Co., Ltd.) and an electroless gold plating solution (Melplate Au-7621, manufactured by Meltex Co., Ltd.) were used. Electroless gold plating was performed to complete the plating process.
After the plating step, the plating protective tape was peeled off by irradiating with 2000 mJ / cm 2 ultraviolet rays from the substrate side of the plating protective tape. At this time, when it was not able to peel, it evaluated as "x".
同様のめっき処理を、同じめっき液を用いて１０００枚行った。得られためっき処理後のウエハのめっき処理面を、顕微鏡を用いて５００倍にて観察し、めっき不良の有無を確認した。
めっき開始１枚目から、１０００枚目まで、めっき不良が１件も発生しなかった場合を「○」と、１件でもめっき不良が発生した場合を「×」と評価した。
結果を表１に示した。 The same plating process was performed 1000 sheets using the same plating solution. The plating treatment surface of the obtained wafer after the plating treatment was observed at 500 times using a microscope to confirm the presence or absence of plating defects.
From the first plating start to the 1000th plating, the case where no plating failure occurred was evaluated as “◯”, and the case where even one plating failure occurred was evaluated as “x”.
The results are shown in Table 1.
めっき開始１枚目から、１０００枚目まで、めっき不良が１件も発生しなかった場合を「○」と、１件でもめっき不良が発生した場合を「×」と評価した。
結果を表１に示した。 The same plating process was performed 1000 sheets using the same plating solution. The plating treatment surface of the obtained wafer after the plating treatment was observed at 500 times using a microscope to confirm the presence or absence of plating defects.
From the first plating start to the 1000th plating, the case where no plating failure occurred was evaluated as “◯”, and the case where even one plating failure occurred was evaluated as “x”.
The results are shown in Table 1.
（実施例１）
（１）光硬化型粘着剤の調製
下記の化合物を酢酸エチルに溶解させ、紫外線を照射して重合を行い、重量平均分子量５０万の共重合体からなる光硬化性粘着剤の酢酸エチル溶液を得た。
エチルアクリレート ７５重量部
メチルメタクリレート ２０重量部
アクリル酸 ３重量部
２－ヒドロキシエチルアクリレート ２重量部
光重合開始剤 １重量部
（イルガキュア６５１、５０％酢酸エチル溶液）
ラウリルメルカプタン ０．０１重量部 Example 1
(1) Preparation of photocurable pressure-sensitive adhesive The following compounds are dissolved in ethyl acetate, polymerized by irradiating ultraviolet rays, and an ethyl acetate solution of a photocurable pressure-sensitive adhesive made of a copolymer having a weight average molecular weight of 500,000 is prepared. Obtained.
Ethyl acrylate 75 parts by weight Methyl methacrylate 20 parts by weight Acrylic acid 3 parts by weight 2-hydroxyethyl acrylate 2 parts by weight Photopolymerization initiator 1 part by weight (Irgacure 651, 50% ethyl acetate solution)
Lauryl mercaptan 0.01 parts by weight
（１）光硬化型粘着剤の調製
下記の化合物を酢酸エチルに溶解させ、紫外線を照射して重合を行い、重量平均分子量５０万の共重合体からなる光硬化性粘着剤の酢酸エチル溶液を得た。
エチルアクリレート ７５重量部
メチルメタクリレート ２０重量部
アクリル酸 ３重量部
２－ヒドロキシエチルアクリレート ２重量部
光重合開始剤 １重量部
（イルガキュア６５１、５０％酢酸エチル溶液）
ラウリルメルカプタン ０．０１重量部 Example 1
(1) Preparation of photocurable pressure-sensitive adhesive The following compounds are dissolved in ethyl acetate, polymerized by irradiating ultraviolet rays, and an ethyl acetate solution of a photocurable pressure-sensitive adhesive made of a copolymer having a weight average molecular weight of 500,000 is prepared. Obtained.
Ethyl acrylate 75 parts by weight Methyl methacrylate 20 parts by weight Acrylic acid 3 parts by weight 2-hydroxyethyl acrylate 2 parts by weight Photopolymerization initiator 1 part by weight (Irgacure 651, 50% ethyl acetate solution)
Lauryl mercaptan 0.01 parts by weight
（２）粘着剤層用組成物溶液の調製
得られた光硬化性粘着剤の酢酸エチル溶液の樹脂固形分１００重量部に対して、２－イソシアナトエチルメタクリレート３．５重量部を加えて反応させ、更に、反応後の酢酸エチル溶液の樹脂固形分１００重量部に対して、光重合開始剤としてオリゴ｛２－ヒドロキシ－２－メチル－１－〔４－（１－メチルビニル）フェニル〕プロパン－オン｝（ランベルティ社製、エサキュアワン）２重量部、ポリイソシアネート０．５重量部を混合し粘着剤層用組成物溶液を調製した。 (2) Preparation of composition solution for pressure-sensitive adhesive layer The reaction was conducted by adding 3.5 parts by weight of 2-isocyanatoethyl methacrylate to 100 parts by weight of the resin solid content of the obtained photocurable pressure-sensitive adhesive in ethyl acetate. Furthermore, oligo {2-hydroxy-2-methyl-1- [4- (1-methylvinyl) phenyl] propane is used as a photopolymerization initiator for 100 parts by weight of the resin solid content of the ethyl acetate solution after the reaction. -ON} (Lamberti Co., Esacure One) 2 parts by weight and polyisocyanate 0.5 parts by weight were mixed to prepare a composition solution for an adhesive layer.
得られた光硬化性粘着剤の酢酸エチル溶液の樹脂固形分１００重量部に対して、２－イソシアナトエチルメタクリレート３．５重量部を加えて反応させ、更に、反応後の酢酸エチル溶液の樹脂固形分１００重量部に対して、光重合開始剤としてオリゴ｛２－ヒドロキシ－２－メチル－１－〔４－（１－メチルビニル）フェニル〕プロパン－オン｝（ランベルティ社製、エサキュアワン）２重量部、ポリイソシアネート０．５重量部を混合し粘着剤層用組成物溶液を調製した。 (2) Preparation of composition solution for pressure-sensitive adhesive layer The reaction was conducted by adding 3.5 parts by weight of 2-isocyanatoethyl methacrylate to 100 parts by weight of the resin solid content of the obtained photocurable pressure-sensitive adhesive in ethyl acetate. Furthermore, oligo {2-hydroxy-2-methyl-1- [4- (1-methylvinyl) phenyl] propane is used as a photopolymerization initiator for 100 parts by weight of the resin solid content of the ethyl acetate solution after the reaction. -ON} (Lamberti Co., Esacure One) 2 parts by weight and polyisocyanate 0.5 parts by weight were mixed to prepare a composition solution for an adhesive layer.
（３）めっき保護テープの製造
得られた粘着剤層用組成物溶液を、片面にコロナ処理を施した厚さ７５μｍの透明なポリエチレンテレフタレート（ＰＥＴ）フィルムのコロナ処理上に乾燥皮膜の厚さが約１５μｍとなるようにドクターナイフで塗工し１１０℃、５分間加熱して塗工溶液を乾燥させた。乾燥後の粘着剤層は乾燥状態で粘着性を示した。次いで、粘着剤層の表面に離型処理が施されたＰＥＴフィルムを貼り付けた。その後、４０℃、３日間静置養生を行い、めっき保護テープを得た。 (3) Manufacture of plating protective tape The composition solution for the pressure-sensitive adhesive layer obtained was subjected to corona treatment on a transparent polyethylene terephthalate (PET) film having a thickness of 75 μm and subjected to corona treatment on one side. The coating solution was dried with a doctor knife so as to be about 15 μm and heated at 110 ° C. for 5 minutes. The pressure-sensitive adhesive layer after drying showed adhesiveness in a dry state. Next, a PET film that was subjected to a release treatment was attached to the surface of the pressure-sensitive adhesive layer. Then, stationary curing was performed at 40 ° C. for 3 days to obtain a plating protective tape.
得られた粘着剤層用組成物溶液を、片面にコロナ処理を施した厚さ７５μｍの透明なポリエチレンテレフタレート（ＰＥＴ）フィルムのコロナ処理上に乾燥皮膜の厚さが約１５μｍとなるようにドクターナイフで塗工し１１０℃、５分間加熱して塗工溶液を乾燥させた。乾燥後の粘着剤層は乾燥状態で粘着性を示した。次いで、粘着剤層の表面に離型処理が施されたＰＥＴフィルムを貼り付けた。その後、４０℃、３日間静置養生を行い、めっき保護テープを得た。 (3) Manufacture of plating protective tape The composition solution for the pressure-sensitive adhesive layer obtained was subjected to corona treatment on a transparent polyethylene terephthalate (PET) film having a thickness of 75 μm and subjected to corona treatment on one side. The coating solution was dried with a doctor knife so as to be about 15 μm and heated at 110 ° C. for 5 minutes. The pressure-sensitive adhesive layer after drying showed adhesiveness in a dry state. Next, a PET film that was subjected to a release treatment was attached to the surface of the pressure-sensitive adhesive layer. Then, stationary curing was performed at 40 ° C. for 3 days to obtain a plating protective tape.
（実施例２）
光重合開始剤を２－ヒドロキシ－２－メチル－１－フェニル－プロパン－１－オン（チバ・スペシャルティ・ケミカルズ社製、ダロキュア１１７３）２重量部に代えた以外は実施例１と同様にして、めっき保護テープを得た。 (Example 2)
Except that the photopolymerization initiator was replaced with 2 parts by weight of 2-hydroxy-2-methyl-1-phenyl-propan-1-one (Ciba Specialty Chemicals, Darocur 1173), the same as in Example 1, A plating protective tape was obtained.
光重合開始剤を２－ヒドロキシ－２－メチル－１－フェニル－プロパン－１－オン（チバ・スペシャルティ・ケミカルズ社製、ダロキュア１１７３）２重量部に代えた以外は実施例１と同様にして、めっき保護テープを得た。 (Example 2)
Except that the photopolymerization initiator was replaced with 2 parts by weight of 2-hydroxy-2-methyl-1-phenyl-propan-1-one (Ciba Specialty Chemicals, Darocur 1173), the same as in Example 1, A plating protective tape was obtained.
（比較例１）
光重合開始剤を２－ベンジル－２－ジメチルアミノ－１－（４－モルフォリノフェニル）－ブタノン－１（チバ・スペシャルティ・ケミカルズ社製、イルガキュア３６９）２重量部に代えた以外は実施例１と同様にして、めっき保護テープを得た。 (Comparative Example 1)
Example 1 except that the photopolymerization initiator was changed to 2 parts by weight of 2-benzyl-2-dimethylamino-1- (4-morpholinophenyl) -butanone-1 (manufactured by Ciba Specialty Chemicals, Irgacure 369). In the same manner as above, a plating protective tape was obtained.
光重合開始剤を２－ベンジル－２－ジメチルアミノ－１－（４－モルフォリノフェニル）－ブタノン－１（チバ・スペシャルティ・ケミカルズ社製、イルガキュア３６９）２重量部に代えた以外は実施例１と同様にして、めっき保護テープを得た。 (Comparative Example 1)
Example 1 except that the photopolymerization initiator was changed to 2 parts by weight of 2-benzyl-2-dimethylamino-1- (4-morpholinophenyl) -butanone-1 (manufactured by Ciba Specialty Chemicals, Irgacure 369). In the same manner as above, a plating protective tape was obtained.
（比較例２）
光重合開始剤を２－メチル－１－〔４－（メチルチオ）フェニル〕－２－モルフォリノプロパン－１－オン（チバ・スペシャルティ・ケミカルズ社製、イルガキュア９０７）２重量部に代えた以外は実施例１と同様にして、めっき保護テープを得た。 (Comparative Example 2)
Implemented except that the photopolymerization initiator was replaced with 2 parts by weight of 2-methyl-1- [4- (methylthio) phenyl] -2-morpholinopropan-1-one (Ciba Specialty Chemicals, Irgacure 907) In the same manner as in Example 1, a plating protective tape was obtained.
光重合開始剤を２－メチル－１－〔４－（メチルチオ）フェニル〕－２－モルフォリノプロパン－１－オン（チバ・スペシャルティ・ケミカルズ社製、イルガキュア９０７）２重量部に代えた以外は実施例１と同様にして、めっき保護テープを得た。 (Comparative Example 2)
Implemented except that the photopolymerization initiator was replaced with 2 parts by weight of 2-methyl-1- [4- (methylthio) phenyl] -2-morpholinopropan-1-one (Ciba Specialty Chemicals, Irgacure 907) In the same manner as in Example 1, a plating protective tape was obtained.
（比較例３）
光重合開始剤をビス（２，４，６－トリメチルベンゾイル）フェニルフォスフィンオキサイド（チバ・スペシャルティ・ケミカルズ社製、イルガキュア８１９）２重量部に代えた以外は実施例１と同様にして、めっき保護テープを得た。 (Comparative Example 3)
Plating protection was carried out in the same manner as in Example 1 except that the photopolymerization initiator was replaced with 2 parts by weight of bis (2,4,6-trimethylbenzoyl) phenylphosphine oxide (manufactured by Ciba Specialty Chemicals, Irgacure 819). I got a tape.
光重合開始剤をビス（２，４，６－トリメチルベンゾイル）フェニルフォスフィンオキサイド（チバ・スペシャルティ・ケミカルズ社製、イルガキュア８１９）２重量部に代えた以外は実施例１と同様にして、めっき保護テープを得た。 (Comparative Example 3)
Plating protection was carried out in the same manner as in Example 1 except that the photopolymerization initiator was replaced with 2 parts by weight of bis (2,4,6-trimethylbenzoyl) phenylphosphine oxide (manufactured by Ciba Specialty Chemicals, Irgacure 819). I got a tape.
（評価）
実施例及び比較例で製造しためっき保護テープについて、以下の方法により評価を行った。 (Evaluation)
About the plating protective tape manufactured by the Example and the comparative example, it evaluated by the following method.
実施例及び比較例で製造しためっき保護テープについて、以下の方法により評価を行った。 (Evaluation)
About the plating protective tape manufactured by the Example and the comparative example, it evaluated by the following method.
厚さ２００μｍ、直径１５０ｍｍのＳｉウエハの片面に、実施例及び比較例で製造しためっき保護テープを貼り合わせた後、２３℃で２０分静置した。その後、ウエハの外周に沿って、めっき保護テープのはみ出し量が０．５ｍｍとなるようにめっき保護テープを切断した。なお、めっき保護テープのはみ出し量を０．５ｍｍ未満としようとすると、ウエハが破損してしまうことがあった。
The plating protective tapes produced in Examples and Comparative Examples were bonded to one side of a Si wafer having a thickness of 200 μm and a diameter of 150 mm, and then allowed to stand at 23 ° C. for 20 minutes. Thereafter, the plating protective tape was cut along the outer periphery of the wafer so that the protruding amount of the plating protective tape was 0.5 mm. If the amount of protrusion of the plating protective tape is less than 0.5 mm, the wafer may be damaged.
めっき保護テープにより保護されたウエハのめっきを施す面に、メルクリーナーＳＣ－７００１（メルテックス株式会社製）を用いて脱脂処理し、メルプレートＥ－７１２１（メルテックス株式会社製）を用いてエッチング処理を行った後、メルプレートコンディショナー７２３０（メルテックス株式会社製）を用いてコンディショニングを行った。次いで、メルプレートＦＺ－７３５０（メルテックス株式会社製）を用いて第１亜鉛置換処理を行い、３０ｗｔ％の硝酸を用いた亜鉛剥離を行い、メルプレートＦＢＺ（メルテックス株式会社製）を用いて第２亜鉛置換処理を行った。次いで、無電解ニッケルめっき液（メルプレートＮＩ－８６９、メルテックス株式会社製）を用いた無電解ニッケルめっきと、無電解金めっき液（メルプレートＡｕ－７６２１、メルテックス株式会社製）を用いた無電解金めっきを行い、めっき工程を完了した。
最後に、めっき保護テープの基材側から２０００ｍＪ／ｃｍ２の紫外線を照射して、めっき保護テープを剥離した。 The surface to be plated of the wafer protected by the plating protective tape is degreased using Mel Cleaner SC-7001 (Meltex Co., Ltd.) and etched using Mel Plate E-7121 (Meltex Co., Ltd.). After the treatment, conditioning was performed using Melplate Conditioner 7230 (Meltex Co., Ltd.). Next, a first zinc replacement treatment was performed using Melplate FZ-7350 (Meltex Co., Ltd.), zinc peeling using 30 wt% nitric acid was performed, and Melplate FBZ (Meltex Co., Ltd.) was used. A second zinc replacement treatment was performed. Next, electroless nickel plating using an electroless nickel plating solution (Melplate NI-869, manufactured by Meltex Co., Ltd.) and an electroless gold plating solution (Melplate Au-7621, manufactured by Meltex Co., Ltd.) were used. Electroless gold plating was performed to complete the plating process.
Finally, 2000 mJ / cm 2 of ultraviolet light was irradiated from the substrate side of the plating protective tape to peel off the plating protective tape.
最後に、めっき保護テープの基材側から２０００ｍＪ／ｃｍ２の紫外線を照射して、めっき保護テープを剥離した。 The surface to be plated of the wafer protected by the plating protective tape is degreased using Mel Cleaner SC-7001 (Meltex Co., Ltd.) and etched using Mel Plate E-7121 (Meltex Co., Ltd.). After the treatment, conditioning was performed using Melplate Conditioner 7230 (Meltex Co., Ltd.). Next, a first zinc replacement treatment was performed using Melplate FZ-7350 (Meltex Co., Ltd.), zinc peeling using 30 wt% nitric acid was performed, and Melplate FBZ (Meltex Co., Ltd.) was used. A second zinc replacement treatment was performed. Next, electroless nickel plating using an electroless nickel plating solution (Melplate NI-869, manufactured by Meltex Co., Ltd.) and an electroless gold plating solution (Melplate Au-7621, manufactured by Meltex Co., Ltd.) were used. Electroless gold plating was performed to complete the plating process.
Finally, 2000 mJ / cm 2 of ultraviolet light was irradiated from the substrate side of the plating protective tape to peel off the plating protective tape.
同様のめっき処理を、同じめっき液を用いて２０００枚行った。得られためっき処理後のウエハのめっき処理面を顕微鏡を用いて５００倍にて観察し、めっき不良の有無を確認した。
めっき開始１枚目から、５００枚目、１０００枚目、１５００枚目及び２０００枚目までのめっき不良発生の有無を表２に示した。 The same plating treatment was performed 2000 sheets using the same plating solution. The plated surface of the obtained wafer after the plating treatment was observed at 500 times using a microscope to confirm the presence or absence of plating defects.
Table 2 shows the presence or absence of defective plating from the first plate to the 500th, 1000th, 1500th and 2000th plates.
めっき開始１枚目から、５００枚目、１０００枚目、１５００枚目及び２０００枚目までのめっき不良発生の有無を表２に示した。 The same plating treatment was performed 2000 sheets using the same plating solution. The plated surface of the obtained wafer after the plating treatment was observed at 500 times using a microscope to confirm the presence or absence of plating defects.
Table 2 shows the presence or absence of defective plating from the first plate to the 500th, 1000th, 1500th and 2000th plates.
本発明によれば、使用後は容易に剥離可能であり、かつ、めっき不良の発生を防止できるめっき保護テープを提供することができる。
ADVANTAGE OF THE INVENTION According to this invention, the plating protective tape which can be peeled easily after use and can prevent generation | occurrence | production of a plating defect can be provided.
ADVANTAGE OF THE INVENTION According to this invention, the plating protective tape which can be peeled easily after use and can prevent generation | occurrence | production of a plating defect can be provided.
Claims (4)
- 無電解めっき法又は電解めっき法によるめっきの際に非めっき面を保護するためのめっき保護テープであって、
基材と、前記基材の少なくとも一方の面に形成された光硬化型粘着剤と光重合開始剤とを含有する粘着剤層とからなり、前記光重合開始剤の分子量をｘ、前記粘着剤層中における前記光硬化型粘着剤１００重量部に対する前記光重合開始剤の配合量をｙ重量部としたときに、ｘとｙとが図１の破線で囲まれた範囲内である
ことを特徴とするめっき保護テープ。 A plating protective tape for protecting the non-plated surface during plating by electroless plating or electrolytic plating,
And a pressure-sensitive adhesive layer containing a photocurable pressure-sensitive adhesive and a photopolymerization initiator formed on at least one surface of the base material, wherein the molecular weight of the photopolymerization initiator is x, and the pressure-sensitive adhesive 1 and x are within the range surrounded by the broken line in FIG. 1, when the blending amount of the photopolymerization initiator with respect to 100 parts by weight of the photocurable pressure-sensitive adhesive in the layer is y parts by weight. Plating protective tape. - 粘着剤層は、光を照射することにより気体を発生する気体発生剤を特徴とする請求項１記載のめっき保護テープ。 The plating protective tape according to claim 1, wherein the pressure-sensitive adhesive layer is a gas generating agent that generates gas when irradiated with light.
- 無電解めっき法又は電解めっき法によるめっきの際に非めっき面を保護するためのめっき保護テープであって、
基材と、前記基材の少なくとも一方の面に形成された光硬化型樹脂と光重合開始剤とを含有する粘着剤層とからなり、前記光重合開始剤は、分子末端に水酸基を有するものである
ことを特徴とするめっき保護テープ。 A plating protective tape for protecting the non-plated surface during plating by electroless plating or electrolytic plating,
A substrate and a pressure-sensitive adhesive layer containing a photocurable resin and a photopolymerization initiator formed on at least one surface of the substrate, and the photopolymerization initiator has a hydroxyl group at the molecular end The plating protective tape characterized by being. - 粘着剤層は、光を照射することにより気体を発生する気体発生剤を特徴とする請求項３記載のめっき保護テープ。
The plating protective tape according to claim 3, wherein the pressure-sensitive adhesive layer is a gas generating agent that generates gas when irradiated with light.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2010511002A JPWO2011001713A1 (en) | 2009-06-29 | 2010-03-08 | Plating protective tape |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2009-154003 | 2009-06-29 | ||
| JP2009154003 | 2009-06-29 | ||
| JP2009155972 | 2009-06-30 | ||
| JP2009-155972 | 2009-06-30 |
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| WO2011001713A1 true WO2011001713A1 (en) | 2011-01-06 |
Family
ID=43410797
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP2010/053779 WO2011001713A1 (en) | 2009-06-29 | 2010-03-08 | Protection tape for plating |
Country Status (2)
| Country | Link |
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| JP (2) | JPWO2011001713A1 (en) |
| WO (1) | WO2011001713A1 (en) |
Cited By (3)
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| US9447288B2 (en) | 2011-09-29 | 2016-09-20 | Lg Chem, Ltd. | Anti-reflective coating composition providing improved scratch resistance, anti-reflective film using the same, and manufacturing method thereof |
| RU2672257C2 (en) * | 2014-09-26 | 2018-11-13 | Чанчжоу Иньшэн Фармасьютикал Ко., Лтд. | Analogue of benzofurane as ns4b inhibitor |
| JP2020158656A (en) * | 2019-03-27 | 2020-10-01 | リンテック株式会社 | Tacky adhesive sheet for workpiece processing |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN110616053A (en) * | 2018-06-19 | 2019-12-27 | 无锡市祁达胶粘带有限公司 | Electroplating film adhesive formula and preparation method thereof |
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Also Published As
| Publication number | Publication date |
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| JP2011026595A (en) | 2011-02-10 |
| JPWO2011001713A1 (en) | 2012-12-13 |
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