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WO2015190230A1 - Dicing sheet - Google Patents

Dicing sheet Download PDF

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Publication number
WO2015190230A1
WO2015190230A1 PCT/JP2015/064181 JP2015064181W WO2015190230A1 WO 2015190230 A1 WO2015190230 A1 WO 2015190230A1 JP 2015064181 W JP2015064181 W JP 2015064181W WO 2015190230 A1 WO2015190230 A1 WO 2015190230A1
Authority
WO
WIPO (PCT)
Prior art keywords
adhesive layer
sensitive adhesive
pressure
dicing sheet
base material
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/JP2015/064181
Other languages
French (fr)
Japanese (ja)
Inventor
尚哉 佐伯
山本 大輔
裕之 米山
洋一 稲男
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Lintec Corp
Original Assignee
Lintec Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=54833335&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=WO2015190230(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Lintec Corp filed Critical Lintec Corp
Priority to JP2016527710A priority Critical patent/JP6319438B2/en
Priority to CN201580030575.0A priority patent/CN106463375B/en
Priority to KR1020167020119A priority patent/KR102355108B1/en
Priority to MYPI2016704523A priority patent/MY181207A/en
Priority to CN201910444689.XA priority patent/CN110211912B/en
Priority to SG11201609451VA priority patent/SG11201609451VA/en
Publication of WO2015190230A1 publication Critical patent/WO2015190230A1/en
Priority to PH12016502287A priority patent/PH12016502287A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J201/00Adhesives based on unspecified macromolecular compounds
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00Adhesives in the form of films or foils
    • C09J7/20Adhesives in the form of films or foils characterised by their carriers
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00Adhesives in the form of films or foils
    • C09J7/20Adhesives in the form of films or foils characterised by their carriers
    • C09J7/22Plastics; Metallised plastics
    • C09J7/24Plastics; Metallised plastics based on macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • C09J7/241Polyolefin, e.g.rubber
    • C09J7/243Ethylene or propylene polymers
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2301/00Additional features of adhesives in the form of films or foils
    • C09J2301/10Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet
    • C09J2301/12Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the arrangement of layers
    • C09J2301/122Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the arrangement of layers the adhesive layer being present only on one side of the carrier, e.g. single-sided adhesive tape
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2301/00Additional features of adhesives in the form of films or foils
    • C09J2301/30Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier
    • C09J2301/312Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier parameters being the characterizing feature

Definitions

  • the present invention relates to a dicing sheet that can be used for dicing a workpiece such as a semiconductor wafer, particularly stealth dicing.
  • a laminated pressure-sensitive adhesive sheet (two layers of pressure-sensitive adhesive sheets composed of a base material and a pressure-sensitive adhesive layer) is attached to an ultrathin semiconductor wafer, and the laminated pressure-sensitive adhesive sheet is used from the side of the laminated pressure-sensitive adhesive sheet. After irradiating the semiconductor wafer with laser light and forming a modified portion inside the semiconductor wafer, the adhesive sheet is expanded to divide the semiconductor wafer along the dicing line and produce semiconductor chips. A stealth dicing method is disclosed.
  • the laser beam when irradiating a workpiece with laser light, the laser beam needs to pass through the adhesive sheet to reach the workpiece, and therefore the adhesive sheet is required to have laser beam transparency.
  • a release sheet is often laminated on the side of the dicing sheet opposite to the base material of the adhesive layer in order to protect the adhesive layer.
  • a dicing sheet is unwound from the roll state, the surface of the rolled dicing sheet opposite to the adhesive layer of the base material and the surface of the release sheet opposite to the adhesive layer are in close contact with each other, thereby blocking. It may occur, and a feeding failure from the roll may occur, or the substrate may be transferred to a release sheet on which the substrate is wound, so that the workpiece cannot be attached.
  • the present invention has been made in view of the actual situation as described above, and can suppress the occurrence of blocking when the dicing sheet is unwound from the roll-up state, and transmits laser light when irradiated with laser light.
  • An object of the present invention is to provide a dicing sheet having excellent properties.
  • the present invention provides a base material, a pressure-sensitive adhesive layer laminated on the first surface side of the base material, and a surface of the pressure-sensitive adhesive layer opposite to the base material.
  • a dicing sheet including a release sheet laminated on the side, wherein the arithmetic average roughness (Ra1) of the second surface of the base material is 0.2 ⁇ m or more, and the second surface of the base material
  • the dicing sheet is characterized in that the arithmetic average roughness (Ra2) after heating the dicing sheet at 130 ° C. for 2 hours is 0.25 ⁇ m or less (Invention 1).
  • the “sheet” includes, for example, a concept of a long tape or the like.
  • invention 1 when the dicing sheet is wound up in a roll shape, the second surface of the base material and the release sheet that comes into contact with the second surface of the base material are hardly adhered, Blocking is unlikely to occur when the rolled-up dicing sheet is fed out. Further, after the dicing sheet is heated, when the laser beam is irradiated from the second surface side of the substrate, the laser beam is transmitted through the dicing sheet without being disturbed by the unevenness of the second surface of the substrate, Efficiently reaches (semiconductor wafer) and has excellent laser beam transmissivity.
  • the arithmetic average roughness (Ra2) after the heating on the second surface of the substrate is preferably smaller than the arithmetic average roughness (Ra1) (Invention 2).
  • the base material preferably has a melting point of 90 to 180 ° C. (Invention 3).
  • the storage elastic modulus of the substrate at 130 ° C. is preferably 1 to 100 MPa (Invention 4).
  • the light transmittance of the substrate after the heating at a wavelength of 1064 nm is preferably 40% or more (Invention 5).
  • the substrate is preferably a film composed of a copolymer of ethylene and propylene (Invention 6).
  • the dicing sheet preferably includes a jig pressure-sensitive adhesive layer laminated on a peripheral edge of the pressure-sensitive adhesive layer on the side opposite to the base material side (Invention 7). .
  • the dicing sheet according to the present invention it is possible to suppress the occurrence of blocking when the dicing sheet is unwound from the state of being wound up in a roll shape, and is excellent in laser light transmittance when irradiated with laser light.
  • FIG. 1 is a cross-sectional view of a dicing sheet according to an embodiment of the present invention.
  • the dicing sheet 1 according to the present embodiment includes a base material 2, a pressure-sensitive adhesive layer 3 laminated on the first surface side of the base material 2 (upper side in FIG. 1), and a pressure-sensitive adhesive. And a release sheet 6 laminated on the layer 3.
  • the release sheet 6 is peeled and removed when the dicing sheet 1 is used, and protects the pressure-sensitive adhesive layer 3 until then.
  • the surface of the base material 2 on the pressure-sensitive adhesive layer 3 side is referred to as a “first surface”
  • the opposite surface the lower surface in FIG. 1 is referred to as a “second surface”.
  • the dicing sheet 1 according to the present embodiment is used, as an example, for holding a semiconductor wafer during dicing of a semiconductor wafer as a workpiece, but is not limited thereto.
  • the dicing sheet 1 according to the present embodiment is usually formed in a long shape, wound into a roll, and used in a roll-to-roll manner.
  • the arithmetic average roughness (Ra1) on the second surface of the base material 2 (hereinafter sometimes referred to as “the back surface of the base material 2”) is 0.2 ⁇ m or more.
  • the arithmetic average roughness (Ra2) on the back surface of the substrate 2 after heating the dicing sheet 1 at 130 ° C. for 2 hours and cooling to room temperature (hereinafter sometimes simply referred to as “after heating”) is 0. 25 ⁇ m or less.
  • the arithmetic mean roughness (Ra1) of the back surface of the base material 2 is the arithmetic average roughness of the back surface of the base material 2 before heating at 130 ° C.
  • arithmetic average roughness before heating is hereinafter referred to as “arithmetic average roughness before heating”.
  • Ra1 ".
  • the arithmetic average roughness (Ra1) before heating and the arithmetic average roughness (Ra2) after heating are measured based on JIS B0601: 2001, and the details of the measuring method are as shown in the test examples described later. is there.
  • Arithmetic average roughness (Ra1) before heating of the back surface of the base material 2 is 0.2 ⁇ m or more, so that the back surface of the base material 2 and the surface opposite to the adhesive layer 3 of the release sheet 6 are in close contact with each other. Difficult. Thereby, blocking is hard to generate
  • the arithmetic average roughness (Ra1) before heating on the back surface of the substrate 2 is preferably 0.25 ⁇ m or more, and particularly preferably 0.30 ⁇ m or more.
  • the upper limit of the arithmetic average roughness (Ra1) before heating on the back surface of the substrate 2 is preferably 1.0 ⁇ m or less, particularly preferably 0.8 ⁇ m or less, and more preferably 0.7 ⁇ m.
  • the following is preferable. If the arithmetic average roughness (Ra1) before heating exceeds 1.0 ⁇ m, it may be difficult to satisfy the arithmetic average roughness (Ra2) after heating described above. That is, the arithmetic average roughness (Ra1) before heating on the back surface of the substrate 41 is preferably in the range of 0.25 to 1.0 ⁇ m, and more preferably in the range of 0.30 to 0.7 ⁇ m. .
  • the laser beam was irradiated from the back side of the base material 2 after the dicing sheet 1 was heated.
  • the laser beam passes through the dicing sheet 1 without being disturbed by the unevenness on the back surface of the base material 2, efficiently reaches the workpiece (semiconductor wafer), and has excellent laser beam transparency. Therefore, it is excellent in the work division property by stealth dicing.
  • the arithmetic average roughness (Ra2) after heating on the back surface of the substrate 2 is preferably 0.20 ⁇ m or less, and particularly preferably 0.10 ⁇ m or less.
  • the lower limit of the arithmetic average roughness (Ra2) after heating on the back surface of the substrate 2 is not particularly limited as long as the arithmetic average roughness (Ra1) before heating is satisfied. However, it is usually 0.001 ⁇ m or more, preferably 0.01 ⁇ m or more. That is, the arithmetic average roughness (Ra2) after heating on the back surface of the substrate 41 is preferably in the range of 0.001 to 0.20 ⁇ m, and more preferably in the range of 0.01 to 0.10 ⁇ m. .
  • the arithmetic average roughness (Ra2) after the heating by the said conditions in the back surface of the base material 2 is smaller than the arithmetic average roughness (Ra1) before a heating.
  • arithmetic mean roughness Ra1
  • the roll surface used when forming the resin film which comprises the base material 2 The surface roughness can be changed, sandblasting, or blending of fillers that melt and become flat by heating can be adjusted.
  • the base material 2 is a resin film having a melting point within a predetermined range (a film mainly composed of a resin-based material).
  • a resin film having a melting point within a predetermined range it is preferable to form a resin film having a melting point within a predetermined range and a storage elastic modulus at 130 ° C. within a predetermined range.
  • the melting point of the substrate 2 is preferably 90 to 180 ° C, particularly preferably 100 to 160 ° C, and more preferably 110 to 150 ° C.
  • the arithmetic average roughness (Ra2) after heating on the back surface of the base material 2 can be easily adjusted to the above range. If the melting point of the substrate 2 is less than 90 ° C, the substrate 2 may be completely melted during heating. On the other hand, when the melting point of the base material 2 exceeds 180 ° C., the arithmetic average roughness on the back surface of the base material 2 may not be changed by heating at 130 ° C. for 2 hours.
  • fusing point was measured based on JISK7121 (ISO3146), and the detail of the measuring method is as showing to the test example mentioned later.
  • the base material 2 can adjust mainly by melting
  • the storage elastic modulus of the substrate 2 at 130 ° C. is preferably 1 to 100 MPa, particularly preferably 2 to 80 MPa, and further preferably 5 to 50 MPa.
  • the arithmetic average roughness (Ra2) after heating on the back surface of the base material 2 can be easily adjusted to the above range. If the storage elastic modulus at 130 ° C. of the base material 2 is less than 1 MPa, the base material 2 may be greatly deformed during the heat treatment, and the workpiece may not be held. On the other hand, when the storage elastic modulus at 130 ° C.
  • the measuring method of the said storage elastic modulus is as showing to the test example mentioned later.
  • the method for adjusting the storage elastic modulus of the substrate 2 at 130 ° C. is not particularly limited, but in general, it can be adjusted mainly by the storage elastic modulus of the resin material to be used. In general, even if the chemical structure is the same, if the molecular weight is high, the storage elastic modulus tends to increase, and the storage elastic modulus tends to increase due to cross-linking and narrow molecular weight distribution. Based on this tendency, the base material 2 can be adjusted to an arbitrary storage elastic modulus.
  • the light transmittance at a wavelength of 1064 nm after heating the substrate 2 is preferably 40% or more, particularly preferably 50% or more, and further 60 % Or more is preferable. Since the light transmittance at a wavelength of 1064 nm after the heating of the base material 2 is in the above range, the work can be easily divided by stealth dicing. In this embodiment, when the arithmetic mean roughness (Ra2) after heating on the back surface of the base material 2 is in the above range, the above light transmittance can be realized. The higher the light transmittance at a wavelength of 1064 nm after heating the substrate 2, the better, but the light transmittance that can be realized is about 99% at the maximum.
  • the resin film constituting the substrate 2 include polyethylene films such as low density polyethylene (LDPE) film, linear low density polyethylene (LLDPE) film, and high density polyethylene (HDPE) film, polypropylene film, and ethylene-propylene.
  • polyethylene films such as low density polyethylene (LDPE) film, linear low density polyethylene (LLDPE) film, and high density polyethylene (HDPE) film, polypropylene film, and ethylene-propylene.
  • Polyolefin films such as copolymer film, polybutene film, polybutadiene film, polymethylpentene film, ethylene-norbornene copolymer film, norbornene resin film; ethylene-vinyl acetate copolymer film, ethylene- (meth) acrylic acid copolymer Polymer films, ethylene copolymer films such as ethylene- (meth) acrylate copolymer films; polyvinyl chloride films such as polyvinyl chloride films and vinyl chloride copolymer films Arm, polyethylene terephthalate film, a polyester film such as polyethylene terephthalate and polybutylene terephthalate film; polyurethane film; polyimide film; polystyrene films; polycarbonate films; and fluorine resin film.
  • modified films such as these crosslinked films and ionomer films are also used.
  • a laminated film in which a plurality of the above films are laminated may be used.
  • (meth) acrylic acid in the present specification means both acrylic acid and methacrylic acid. The same applies to other similar terms.
  • a film whose arithmetic average roughness changes before and after heating is disposed on the back side of the base material 2, and the adhesive layer 3 side of the base material 2 has heat resistance and does not deform even at high temperatures. It is preferable to arrange a film.
  • polyolefin film is preferable, polyethylene film, polypropylene film and ethylene-propylene copolymer film are particularly preferable, and ethylene-propylene copolymer film is more preferable.
  • these resin films the above-described physical properties are easily satisfied.
  • the above-described physical properties are satisfied by adjusting the copolymerization ratio of the ethylene monomer and the propylene monomer. easy.
  • these resin films are preferable also from a viewpoint of workpiece sticking property or chip peelability.
  • the resin film is subjected to surface treatment by an oxidation method, a concavo-convex method, or a primer treatment on one side or both sides as desired.
  • an oxidation method examples include corona discharge treatment, plasma discharge treatment, chromium oxidation treatment (wet), flame treatment, hot air treatment, ozone, ultraviolet irradiation treatment, and the like.
  • a thermal spraying method examples include corona discharge treatment, plasma discharge treatment, chromium oxidation treatment (wet), flame treatment, hot air treatment, ozone, ultraviolet irradiation treatment, and the like.
  • the base material 2 may contain various additives, such as a coloring agent, a flame retardant, a plasticizer, an antistatic agent, a lubricant, a filler, in the said resin film.
  • additives such as a coloring agent, a flame retardant, a plasticizer, an antistatic agent, a lubricant, a filler, in the said resin film.
  • the thickness of the substrate 2 is not particularly limited as long as it can function properly in each step in which the dicing sheet 1 is used, but is preferably 20 to 450 ⁇ m, more preferably 25 to 400 ⁇ m, It is preferably 50 to 350 ⁇ m.
  • the pressure-sensitive adhesive layer 3 included in the dicing sheet 1 according to the present embodiment may be made of a non-energy ray-curable pressure-sensitive adhesive or may be made of an energy-ray-curable pressure-sensitive adhesive.
  • the non-energy ray curable pressure-sensitive adhesive those having desired adhesive strength and removability are preferable.
  • Polyvinyl ether-based pressure-sensitive adhesives can be used. Among these, in the dicing process or the like, an acrylic pressure-sensitive adhesive that can effectively prevent the workpiece or workpiece from falling off is preferable.
  • the adhesive strength of the energy ray curable pressure-sensitive adhesive is reduced by energy ray irradiation, when the workpiece or workpiece and the dicing sheet 1 are to be separated, they can be easily separated by irradiation with energy rays. it can.
  • the energy ray-curable pressure-sensitive adhesive constituting the pressure-sensitive adhesive layer 3 may be mainly composed of a polymer having energy ray-curability, or a polymer having no energy ray-curability and an energy ray-curable property.
  • the main component may be a polyfunctional monomer and / or a mixture with an oligomer.
  • the energy ray-curable pressure-sensitive adhesive is mainly composed of a polymer having energy ray-curability.
  • the polymer having energy ray curability is a (meth) acrylic acid ester (co) polymer (A) (hereinafter referred to as “energy ray”) in which a functional group having energy ray curability (energy ray curable group) is introduced into the side chain. It may be referred to as “curable polymer (A)”).
  • This energy ray curable polymer (A) includes a (meth) acrylic copolymer (a1) having a functional group-containing monomer unit, and an unsaturated group-containing compound (a2) having a substituent bonded to the functional group. It is preferable that it is obtained by making it react.
  • the acrylic copolymer (a1) is composed of a structural unit derived from a functional group-containing monomer and a structural unit derived from a (meth) acrylic acid ester monomer or a derivative thereof.
  • the functional group-containing monomer as a constituent unit of the acrylic copolymer (a1) is a monomer having a polymerizable double bond and a functional group such as a hydroxyl group, an amino group, a substituted amino group, or an epoxy group in the molecule. It is preferable that
  • the functional group-containing monomer examples include 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 3-hydroxypropyl (meth) acrylate, 4-hydroxybutyl (meth) acrylate, and the like. These may be used alone or in combination of two or more.
  • Examples of the (meth) acrylic acid ester monomer constituting the acrylic copolymer (a1) include alkyl (meth) acrylates having 1 to 20 carbon atoms in the alkyl group, cycloalkyl (meth) acrylates, and benzyl (meth) acrylates. Is used. Among these, particularly preferred are alkyl (meth) acrylates having an alkyl group having 1 to 18 carbon atoms, such as methyl (meth) acrylate, ethyl (meth) acrylate, propyl (meth) acrylate, n-butyl (meth) ) Acrylate, 2-ethylhexyl (meth) acrylate and the like are used.
  • the structural unit derived from the functional group-containing monomer is usually 3 to 100% by mass, preferably 4 to 80%, based on the total mass of the acrylic copolymer (a1). More preferably, it is contained in a proportion of 5 to 40% by mass, and the structural unit derived from the (meth) acrylic acid ester monomer or derivative thereof is usually based on the total mass of the acrylic copolymer (a1). It is contained in a proportion of 0 to 97% by mass, preferably 60 to 95% by mass.
  • the acrylic copolymer (a1) can be obtained by copolymerizing a functional group-containing monomer as described above with a (meth) acrylic acid ester monomer or a derivative thereof in a conventional manner. Dimethylacrylamide, vinyl formate, vinyl acetate, styrene and the like may be copolymerized.
  • an energy beam curable polymer (A ) Is obtained.
  • the substituent of the unsaturated group-containing compound (a2) can be appropriately selected according to the type of functional group of the functional group-containing monomer unit of the acrylic copolymer (a1).
  • the substituent is preferably an isocyanate group or an epoxy group
  • the substituent is an amino group, a carboxyl group or an aziridinyl group. preferable.
  • the unsaturated group-containing compound (a2) contains 1 to 5, preferably 1 to 2, energy-polymerizable carbon-carbon double bonds per molecule.
  • Specific examples of such unsaturated group-containing compound (a2) include, for example, 2-methacryloyloxyethyl isocyanate, meta-isopropenyl- ⁇ , ⁇ -dimethylbenzyl isocyanate, methacryloyl isocyanate, allyl isocyanate, 1,1- ( Bisacryloyloxymethyl) ethyl isocyanate; acryloyl monoisocyanate compound obtained by reaction of diisocyanate compound or polyisocyanate compound with hydroxyethyl (meth) acrylate; diisocyanate compound or polyisocyanate compound, polyol compound, and hydroxyethyl (meth) Acryloyl monoisocyanate compound obtained by reaction with acrylate; glycidyl (meth) acrylate; (meth) acrylic acid, 2-
  • the unsaturated group-containing compound (a2) is usually used in a ratio of 10 to 100 equivalents, preferably 20 to 95 equivalents per 100 equivalents of the functional group-containing monomer of the acrylic copolymer (a1).
  • the reaction temperature, pressure, solvent, time, presence of catalyst, catalyst can be selected as appropriate.
  • the functional group present in the acrylic copolymer (a1) reacts with the substituent in the unsaturated group-containing compound (a2), so that the unsaturated group is contained in the acrylic copolymer (a1). It introduce
  • the weight average molecular weight of the energy ray curable polymer (A) thus obtained is preferably 10,000 or more, particularly preferably 150,000 to 1,500,000, and more preferably 200,000 to 1,000,000. Is preferred.
  • the weight average molecular weight (Mw) in this specification is the value of polystyrene conversion measured by the gel permeation chromatography method (GPC method).
  • the energy ray-curable pressure-sensitive adhesive has a polymer having energy ray-curability as a main component
  • the energy ray-curable pressure-sensitive adhesive further contains an energy ray-curable monomer and / or oligomer (B). You may contain.
  • the energy ray-curable monomer and / or oligomer (B) for example, an ester of a polyhydric alcohol and (meth) acrylic acid or the like can be used.
  • Examples of the energy ray-curable monomer and / or oligomer (B) include monofunctional acrylic acid esters such as cyclohexyl (meth) acrylate and isobornyl (meth) acrylate, trimethylolpropane tri (meth) acrylate, penta Erythritol tri (meth) acrylate, pentaerythritol tetra (meth) acrylate, dipentaerythritol hexa (meth) acrylate, 1,4-butanediol di (meth) acrylate, 1,6-hexanediol di (meth) acrylate, polyethylene glycol Polyfunctional acrylic esters such as di (meth) acrylate and dimethyloltricyclodecane di (meth) acrylate, polyester oligo (meth) acrylate, polyurethane oligo (meta Acrylate, and the like.
  • monofunctional acrylic acid esters such as
  • the content of the energy ray curable monomer and / or oligomer (B) in the energy ray curable adhesive is determined by the energy ray curable pressure sensitive adhesive.
  • the total mass is preferably 5 to 80% by mass, more preferably 20 to 60% by mass.
  • photopolymerization initiator (C) examples include benzophenone, acetophenone, benzoin, benzoin methyl ether, benzoin ethyl ether, benzoin isopropyl ether, benzoin isobutyl ether, benzoin benzoic acid, benzoin methyl benzoate, benzoin dimethyl ketal, 2,4-diethylthioxanthone, 1-hydroxycyclohexyl phenyl ketone, benzyldiphenyl sulfide, tetramethylthiuram monosulfide, azobisisobutyronitrile, benzyl, dibenzyl, diacetyl, ⁇ -chloranthraquinone, (2,4 6-trimethylbenzyldiphenyl) phosphine oxide, 2-benzothiazole-N, N-diethyldithiocarbamate, oligo ⁇ 2-hydroxy-2-me Le-1- [4-
  • the photopolymerization initiator (C) is energy beam curable copolymer (A) (when energy beam curable monomer and / or oligomer (B) is blended, energy beam curable copolymer (A). , And a total amount of energy ray-curable monomer and / or oligomer (B) of 100 parts by mass) in an amount of 0.1 to 10 parts by mass, in particular 0.5 to 6 parts by mass with respect to 100 parts by mass. Is preferably used.
  • other components may be appropriately blended in addition to the above components.
  • other components include a polymer component or oligomer component (D) that does not have energy beam curability, and a crosslinking agent (E).
  • Examples of the polymer component or oligomer component (D) having no energy ray curability include polyacrylates, polyesters, polyurethanes, polycarbonates, polyolefins, etc., and polymers having a weight average molecular weight (Mw) of 3,000 to 2.5 million. Or an oligomer is preferable.
  • crosslinking agent (E) a polyfunctional compound having reactivity with the functional group of the energy beam curable copolymer (A) or the like can be used.
  • polyfunctional compounds include, for example, isocyanate compounds, epoxy compounds, amine compounds, melamine compounds, aziridine compounds, hydrazine compounds, aldehyde compounds, oxazoline compounds, metal alkoxide compounds, metal chelate compounds, metal salts, Examples thereof include ammonium salts and reactive phenol resins.
  • the pressure-sensitive adhesive layer 3 is hardened and peelable before curing, strength after curing, and adhesion to other layers. , Storage stability and the like can be improved.
  • the blending amount of these other components is not particularly limited, and is appropriately determined in the range of 0 to 40 parts by mass with respect to 100 parts by mass of the energy beam curable copolymer (A).
  • the energy ray-curable adhesive is mainly composed of a mixture of a polymer component having no energy ray curability and an energy ray-curable polyfunctional monomer and / or oligomer will be described below.
  • the polymer component having no energy beam curability for example, the same components as those of the acrylic copolymer (a1) described above can be used.
  • the content of the polymer component having no energy beam curability in the energy beam curable resin composition is preferably 20 to 99.9% by mass with respect to the total mass of the energy beam curable resin composition, In particular, it is preferably 30 to 80% by mass.
  • the energy ray-curable polyfunctional monomer and / or oligomer the same one as the above-mentioned component (B) is selected.
  • the blending ratio of the polymer component having no energy ray curability and the energy ray curable polyfunctional monomer and / or oligomer is 10 to 150 parts by mass of the polyfunctional monomer and / or oligomer with respect to 100 parts by mass of the polymer component.
  • the amount is preferably 25 to 100 parts by mass.
  • the photopolymerization initiator (C) and the crosslinking agent (E) can be appropriately blended as described above.
  • the thickness of the pressure-sensitive adhesive layer 3 is not particularly limited as long as it can function properly in each process in which the dicing sheet 1 is used. Specifically, the thickness of the pressure-sensitive adhesive layer 3 is preferably 1 to 50 ⁇ m, particularly preferably 2 to 30 ⁇ m, and further preferably 3 to 20 ⁇ m.
  • the release sheet 6 in the present embodiment protects the pressure-sensitive adhesive layer 3 until the dicing sheet 1 is used.
  • the release sheet 6 in the present embodiment is directly laminated on the pressure-sensitive adhesive layer 3, but is not limited to this, and other layers (such as a die bonding film) are laminated on the pressure-sensitive adhesive layer 3, A release sheet 6 may be laminated on the other layer.
  • the configuration of the release sheet 6 is arbitrary, and examples include a plastic film that has been subjected to a release treatment with a release agent or the like.
  • the plastic film include polyester films such as polyethylene terephthalate, polybutylene terephthalate, and polyethylene naphthalate, and polyolefin films such as polypropylene and polyethylene.
  • the release agent for example, silicone-based, fluorine-based, long-chain alkyl-based, and the like can be used, and among these, a silicone-based material that can provide inexpensive and stable performance is preferable.
  • the thickness of the release sheet 6 is not particularly limited, but is usually about 20 to 250 ⁇ m.
  • Manufacturing method of dicing sheet In order to manufacture the dicing sheet 1, as an example, an application for the pressure-sensitive adhesive layer containing the pressure-sensitive adhesive constituting the pressure-sensitive adhesive layer 3 and optionally a solvent on the release surface of the release sheet 6. An adhesive is applied and dried to form the pressure-sensitive adhesive layer 3. Then, the base material 2 is crimped
  • the pressure-sensitive adhesive layer 3 in the present embodiment can be attached to a jig such as a ring frame.
  • a jig such as a ring frame.
  • the laminated body of the base material 2 and the pressure-sensitive adhesive layer 3 may have a desired shape, for example, by inserting a cutting blade from the side of the first release sheet or the second release sheet or half-cutting by laser irradiation, as desired. You may form in circular shapes etc. corresponding to a workpiece
  • work semiconductor wafer. In this case, an excess portion generated by the half cut may be removed as appropriate.
  • the rolled-up dicing sheet 1 is unwound and the adhesive layer 3 of the dicing sheet 1 is attached to the semiconductor wafer 7 and the ring frame 8 as shown in FIG.
  • the arithmetic average roughness (Ra1) before heating of the back surface of the substrate 2 is 0.2 ⁇ m or more, blocking is unlikely to occur during the above-described feeding, so that feeding failure occurs. Or it becomes impossible to attach a workpiece.
  • laminated structure L having a configuration in which the semiconductor wafer 7 is laminated on the surface of the expandable dicing sheet 1 on the pressure-sensitive adhesive layer 3 side (hereinafter, sometimes referred to as “laminated structure L”) is obtained.
  • laminated structure L shown in FIG. 2 further includes a ring frame 8.
  • the dicing sheet 1 is subjected to heat treatment.
  • the heating temperature at this time is preferably 50 to 200 ° C., particularly 90 to 150 ° C., and the heating time is preferably 0.1 to 10 hours, particularly 1 to 3 hours.
  • the arithmetic average roughness (Ra2) of the back surface of the substrate 2 is 0.25 ⁇ m or less by the heat treatment.
  • the laminated structure L is subjected to a stealth dicing process.
  • the laminated structure L is installed in a split processing laser irradiation apparatus, the position of the surface of the semiconductor wafer 7 is detected, and then laser light is applied to the semiconductor wafer 7 via the dicing sheet 1. Irradiation forms a modified layer in the semiconductor wafer 7. Thereafter, an expanding process for extending the dicing sheet 1 is performed to apply a force (tensile force in the main surface direction) to the semiconductor wafer 7. As a result, the semiconductor wafer 7 adhered to the dicing sheet 1 is divided to obtain chips. Thereafter, a chip is picked up from the dicing sheet 1 using a pickup device.
  • the arithmetic average roughness (Ra2) after heating of the back surface of the base material 2 is 0.25 ⁇ m or less, so that the laser light transmission is excellent, so in the stealth dicing step, Excellent work division by stealth dicing.
  • FIG. 3 is a cross-sectional view of a dicing sheet according to another embodiment of the present invention.
  • the dicing sheet 1 ⁇ / b> A includes a base material 2, a pressure-sensitive adhesive layer 3 laminated on one surface side (the upper side in FIG. 1), and a pressure-sensitive adhesive layer.
  • 3 includes a jig pressure-sensitive adhesive layer 5 laminated on the peripheral edge opposite to the substrate 2, and a release sheet 6 laminated on the pressure-sensitive adhesive layer 3 and the jig pressure-sensitive adhesive layer 5. Is done.
  • the adhesive layer 5 for jigs is a layer for bonding the dicing sheet 1 to a jig such as a ring frame.
  • the release sheet 6 protects the pressure-sensitive adhesive layer 3 and the jig pressure-sensitive adhesive layer 5 until the dicing sheet 1A is used. That is, the dicing sheet 1A shown in FIG. 3 is obtained by adding the jig adhesive layer 5 to the dicing sheet 1 shown in FIG.
  • tool what has desired adhesive force and removability is preferable, for example, an acrylic adhesive, a rubber adhesive, a silicone adhesive, a urethane adhesive Polyester-based pressure-sensitive adhesives, polyvinyl ether-based pressure-sensitive adhesives, and the like can be used.
  • the adhesive layer 5 for jigs has high adhesiveness with jigs such as a ring frame, and can effectively prevent the dicing sheet 1A from being peeled off from the ring frame or the like in a dicing process or the like. It is preferable to use an acrylic adhesive.
  • the base material as a core material may interpose inside the thickness direction of the adhesive layer 5 for jig
  • the thickness of the pressure-sensitive adhesive layer 5 for jigs is preferably 5 to 200 ⁇ m, particularly preferably 10 to 100 ⁇ m, from the viewpoint of adhesion to a jig such as a ring frame.
  • each member other than the jig adhesive layer 5 are the same as the material and thickness of each member of the dicing sheet 1 described above.
  • a pressure-sensitive adhesive that constitutes the pressure-sensitive adhesive layer 3 and, if desired, a pressure-sensitive adhesive layer-containing coating agent are applied to the release surface of the release sheet.
  • the pressure-sensitive adhesive layer 3 is formed by drying.
  • the base material 2 is crimped
  • the pressure-sensitive adhesive layer 3 when the pressure-sensitive adhesive layer 3 is made of an energy ray-curable pressure-sensitive adhesive, the pressure-sensitive adhesive layer 3 may be irradiated with energy rays at this stage to cure the pressure-sensitive adhesive layer 3. When laminating these layers, the pressure-sensitive adhesive layer 3 may be cured after laminating with other layers. When the pressure-sensitive adhesive layer 3 is cured after being laminated with another layer, the pressure-sensitive adhesive layer 3 may be cured before the dicing step, or the pressure-sensitive adhesive layer 3 may be cured after the dicing step.
  • energy rays ultraviolet rays, electron beams, etc. are usually used. Irradiation of energy rays varies depending on the kind of energy rays, for example, in the case of ultraviolet rays, preferably 50 ⁇ 1000mJ / cm 2 in quantity, especially 100 ⁇ 500mJ / cm 2 preferably. In the case of an electron beam, about 10 to 1000 krad is preferable.
  • the laminate of the base material 2 and the pressure-sensitive adhesive layer 3 may be half-cut if desired, and formed into a desired shape, for example, a shape corresponding to a workpiece (semiconductor wafer). In this case, an excess portion generated by the half cut may be removed as appropriate.
  • the release sheet is peeled off from the pressure-sensitive adhesive layer 3, and a jig pressure-sensitive adhesive layer 5 is formed on the exposed peripheral edge of the pressure-sensitive adhesive layer 3.
  • the jig pressure-sensitive adhesive layer 5 can also be formed by coating in the same manner as the pressure-sensitive adhesive layer 3.
  • a release sheet 6 is laminated on the exposed surfaces of the pressure-sensitive adhesive layer 3 and the jig pressure-sensitive adhesive layer 5 to obtain a dicing sheet 1A.
  • dicing sheet 1A As mentioned above, although one manufacturing method of dicing sheet 1A was shown, it is not limited to this.
  • the jig pressure-sensitive adhesive layer 5 has a base material, after forming a laminate constituting the jig pressure-sensitive adhesive layer 5 on the release sheet, an annular shape corresponding to the jig, etc. It is also possible to make a half cut into the shape and laminate the adhesive layer 3 on the adhesive layer 3.
  • another layer may be interposed between the base material 2 and the pressure-sensitive adhesive layer 3 in the dicing sheets 1 and 1A. Further, another layer may be interposed between the adhesive layer 3 and the release sheet 6 in the dicing sheets 1 and 1A.
  • the other layer include a die bonding film.
  • the dicing sheets 1 and 1A can be used as a dicing die bonding sheet.
  • the arithmetic average roughness (Ra1) before heating on the back surface of the substrate 2 is about 0.51 to 0.65 ⁇ m and heated at 130 ° C. for 2 hours.
  • the storage elastic modulus of the base material 2 at 130 ° C. is set to about 13 to 20 MPa. It will be excellent.
  • Example 1 In Example 1, a dicing sheet 1 as shown in FIGS. 1 and 4 was manufactured as follows.
  • Adhesive main agent (meth) acrylic acid ester copolymer (copolymer obtained by copolymerizing 40 parts by mass of butyl acrylate, 55 parts by mass of 2-ethylhexyl acrylate, and 5 parts by mass of 2-hydroxylethyl acrylate) , Weight average molecular weight: 600,000) 100 parts by mass
  • the arithmetic mean roughness (Ra1) before the heating was adjusted by changing the arithmetic surface roughness of the surface of the metal roll on which the back side was wound up when the substrate was formed.
  • the arithmetic average roughness (Ra2) after the heating was adjusted by changing the copolymerization ratio of ethylene and propylene constituting the ethylene-propylene copolymer of the base material.
  • Examples 2 to 5 and Comparative Examples 1 to 3 The arithmetic average roughness (Ra1) before heating and the arithmetic average roughness (Ra2) after heating, the melting point and the storage elastic modulus at 130 ° C. on the back surface of the base material were changed as shown in Table 1 below. In the same manner as in Example 1, dicing sheets of Examples 2 to 5 and Comparative Examples 1 to 3 were produced.
  • the dicing sheets of the examples and comparative examples provided with the base material were fixed to a ring frame, and in an oven at 130 ° C. in an air atmosphere. After heating for 2 hours, the value after standing to cool to room temperature was measured. During the heat treatment, the measurement surface (the back surface of the base material) was not in contact with the inner wall or bottom of the oven.
  • dissolving peak temperature was calculated
  • Test Example 4 ⁇ Measurement of light transmittance> As shown in Test Example 1, the base materials used in the examples and comparative examples were heated at 130 ° C. for 2 hours, and then the heated base materials were subjected to UV-visible spectrophotometer (manufactured by Shimadzu Corporation, UV- 3101PC (without integrating sphere)), the light transmittance at a wavelength of 200 to 1200 nm was measured, and the measured value at a wavelength of 1064 nm was read. The results are shown in Table 1 below.
  • Step 1 The silicon wafer and the ring frame to which the dicing sheets of Examples and Comparative Examples are attached are placed at predetermined positions of the laser saw so that laser light can be irradiated from the back side of the substrate.
  • Step 2 After detecting the position of the surface of the silicon wafer, the focal position of the laser beam of the laser saw is set, and the planned cutting line is set so that a 9 mm ⁇ 9 mm chip body is formed on the silicon wafer.
  • Step 3 a laser beam having a wavelength of 1064 nm is irradiated from the laser saw 10 times from the back side of the substrate to form a modified layer in the silicon wafer.
  • the silicon wafer and the ring frame to which the dicing sheet is attached are placed on a die separator (DDS 2300, manufactured by Disco Corporation), and expanded at a pulling rate of 100 mm / second and an expanding amount of 10 mm.
  • DDS 2300 die separator
  • the arithmetic average roughness (Ra1) before heating on the back surface of the substrate is 0.2 ⁇ m or more
  • the dicing sheet of the example was excellent in blocking resistance and also in dicing resolution.
  • the dicing sheet according to the present invention is suitably used when it includes a step of irradiating a laser beam so as to transmit the substrate, such as stealth dicing.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Dicing (AREA)
  • Adhesive Tapes (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Laser Beam Processing (AREA)

Abstract

This dicing sheet (1) is provided with a substrate (2), an adhesive layer (3) layered at one surface side of the substrate (2), and a peeling sheet (6) layered at the surface side of the adhesive layer (3) at the reverse of the substrate (2). The arithmetic mean roughness (Ra1) of the second surface of the substrate (2) is at least 0.2 μm, and the arithmetic means roughness (Ra2) of the second surface of the substrate (2) after the dicing sheet (1) is heated for two hours at 130°C is no greater than 0.25 μm.

Description

ダイシングシートDicing sheet

 本発明は、半導体ウエハ等のワークのダイシング、特にステルスダイシングに使用することのできるダイシングシートに関するものである。
本出願は、2014年6月10日に日本に出願された特願2014-120034号に基づき、優先権を主張し、その内容をここに援用する。
The present invention relates to a dicing sheet that can be used for dicing a workpiece such as a semiconductor wafer, particularly stealth dicing.
This application claims priority based on Japanese Patent Application No. 2014-120034 filed in Japan on June 10, 2014, the contents of which are incorporated herein by reference.

 半導体ウエハなどのワークから、半導体チップ等の片状体からなる加工物を製造する際には、従来は、ワークに対し、洗浄等を目的とした液体を吹き付けながら、回転刃でワークを切断して片状体を得るブレードダイシング加工が行われることが一般的であった。しかしながら、近年は、乾式で片状体への分割が可能なステルスダイシング(登録商標;以下同じ)加工が採用されるようになっている(特許文献1)。 When manufacturing a workpiece made of a piece of semiconductor chip or the like from a workpiece such as a semiconductor wafer, conventionally, the workpiece is cut with a rotary blade while spraying a liquid for cleaning or the like on the workpiece. In general, blade dicing is performed to obtain a piece-like body. However, in recent years, stealth dicing (registered trademark; the same applies hereinafter) processing that can be divided into pieces in a dry process has been adopted (Patent Document 1).

 例えば、特許文献2には、積層粘着シート(基材と粘着剤層とからなる粘着シートを2層積層したもの)を極薄の半導体ウエハに貼付し、積層粘着シート側から、この積層粘着シート越しに半導体ウエハに対してレーザ光を照射し、半導体ウエハの内部に改質部を形成した後、粘着シートをエキスパンドすることで、ダイシングラインに沿って半導体ウエハを分割し、半導体チップを生産するステルスダイシング法が開示されている。 For example, in Patent Document 2, a laminated pressure-sensitive adhesive sheet (two layers of pressure-sensitive adhesive sheets composed of a base material and a pressure-sensitive adhesive layer) is attached to an ultrathin semiconductor wafer, and the laminated pressure-sensitive adhesive sheet is used from the side of the laminated pressure-sensitive adhesive sheet. After irradiating the semiconductor wafer with laser light and forming a modified portion inside the semiconductor wafer, the adhesive sheet is expanded to divide the semiconductor wafer along the dicing line and produce semiconductor chips. A stealth dicing method is disclosed.

日本国特許第3762409号公報Japanese Patent No. 3762409 特開2007-123404号公報JP 2007-123404 A

 上記のように、ワークに対してレーザ光を照射する場合、レーザ光は粘着シートを透過してワークに達する必要があるため、粘着シートはレーザ光透過性を有することが要求される。 As described above, when irradiating a workpiece with laser light, the laser beam needs to pass through the adhesive sheet to reach the workpiece, and therefore the adhesive sheet is required to have laser beam transparency.

 ところで、ダイシングシートにおける粘着剤層の基材とは反対側には、前記粘着剤層を保護するために、剥離シートが積層されることが多い。かかるダイシングシートをロールの状態から繰り出すとき、巻き重なったダイシングシートにおける基材の粘着剤層とは反対側の面と、剥離シートの粘着剤層とは反対側の面とが密着してブロッキングが発生し、ロールからの繰り出し不良が生じたり、基材が巻き重なった剥離シートに転写されてしまい、ワークの貼付ができなくなったりすることがある。 Incidentally, a release sheet is often laminated on the side of the dicing sheet opposite to the base material of the adhesive layer in order to protect the adhesive layer. When such a dicing sheet is unwound from the roll state, the surface of the rolled dicing sheet opposite to the adhesive layer of the base material and the surface of the release sheet opposite to the adhesive layer are in close contact with each other, thereby blocking. It may occur, and a feeding failure from the roll may occur, or the substrate may be transferred to a release sheet on which the substrate is wound, so that the workpiece cannot be attached.

 本発明は、上記のような実状に鑑みてなされたものであり、ロール状に巻き取った状態からダイシングシートを繰り出した際のブロッキングの発生を抑制することができ、レーザ光照射時にはレーザ光透過性に優れるダイシングシートを提供することを目的とする。 The present invention has been made in view of the actual situation as described above, and can suppress the occurrence of blocking when the dicing sheet is unwound from the roll-up state, and transmits laser light when irradiated with laser light. An object of the present invention is to provide a dicing sheet having excellent properties.

 上記目的を達成するために、第1に本発明は、基材と、前記基材の第1の面側に積層された粘着剤層と、前記粘着剤層の前記基材とは反対の面側に積層された剥離シートとを備えたダイシングシートであって、前記基材の第2の面における算術平均粗さ(Ra1)は、0.2μm以上であり、前記基材の第2の面における、前記ダイシングシートを130℃で2時間加熱した後の算術平均粗さ(Ra2)は、0.25μm以下であることを特徴とするダイシングシートを提供する(発明1)。なお、本明細書において、「シート」とは、例えば、長尺のテープ等の概念を含むものとする。 In order to achieve the above object, first, the present invention provides a base material, a pressure-sensitive adhesive layer laminated on the first surface side of the base material, and a surface of the pressure-sensitive adhesive layer opposite to the base material. A dicing sheet including a release sheet laminated on the side, wherein the arithmetic average roughness (Ra1) of the second surface of the base material is 0.2 μm or more, and the second surface of the base material The dicing sheet is characterized in that the arithmetic average roughness (Ra2) after heating the dicing sheet at 130 ° C. for 2 hours is 0.25 μm or less (Invention 1). In the present specification, the “sheet” includes, for example, a concept of a long tape or the like.

 上記発明(発明1)によれば、ダイシングシートをロール状に巻き取ったときに、基材の第2の面と、前記基材の第2の面と接触する剥離シートとが密着し難く、巻き取ったロール状のダイシングシートを繰り出す時に、ブロッキングが発生し難い。また、ダイシングシートの加熱後、基材の第2の面側からレーザ光を照射した時に、レーザ光が、基材の第2の面の凹凸で乱されることなくダイシングシートを透過し、ワーク(半導体ウエハ)に効率良く到達し、レーザ光透過性に優れる。 According to the said invention (invention 1), when the dicing sheet is wound up in a roll shape, the second surface of the base material and the release sheet that comes into contact with the second surface of the base material are hardly adhered, Blocking is unlikely to occur when the rolled-up dicing sheet is fed out. Further, after the dicing sheet is heated, when the laser beam is irradiated from the second surface side of the substrate, the laser beam is transmitted through the dicing sheet without being disturbed by the unevenness of the second surface of the substrate, Efficiently reaches (semiconductor wafer) and has excellent laser beam transmissivity.

 上記発明(発明1)において、前記基材の第2の面における前記加熱後の算術平均粗さ(Ra2)は、前記算術平均粗さ(Ra1)より小さいことが好ましい(発明2)。 In the above invention (Invention 1), the arithmetic average roughness (Ra2) after the heating on the second surface of the substrate is preferably smaller than the arithmetic average roughness (Ra1) (Invention 2).

 上記発明(発明1,2)において、前記基材の融点は、90~180℃であることが好ましい(発明3)。 In the above inventions (Inventions 1 and 2), the base material preferably has a melting point of 90 to 180 ° C. (Invention 3).

 上記発明(発明1~3)において、前記基材の130℃における貯蔵弾性率は、1~100MPaであることが好ましい(発明4)。 In the above inventions (Inventions 1 to 3), the storage elastic modulus of the substrate at 130 ° C. is preferably 1 to 100 MPa (Invention 4).

 上記発明(発明1~4)において、前記基材の前記加熱後における波長1064nmの光線透過率は、40%以上であることが好ましい(発明5)。 In the above inventions (Inventions 1 to 4), the light transmittance of the substrate after the heating at a wavelength of 1064 nm is preferably 40% or more (Invention 5).

 上記発明(発明1~5)において、前記基材は、エチレンとプロピレンとの共重合体から構成されるフィルムであることが好ましい(発明6)。 In the above inventions (Inventions 1 to 5), the substrate is preferably a film composed of a copolymer of ethylene and propylene (Invention 6).

 上記発明(発明1~6)において、前記ダイシングシートは、前記粘着剤層の前記基材側とは反対側の周縁部に積層された治具用粘着剤層を備えることが好ましい(発明7)。 In the above inventions (Inventions 1 to 6), the dicing sheet preferably includes a jig pressure-sensitive adhesive layer laminated on a peripheral edge of the pressure-sensitive adhesive layer on the side opposite to the base material side (Invention 7). .

 本発明に係るダイシングシートによれば、ロール状に巻き取った状態から前記ダイシングシートを繰り出した際のブロッキングの発生を抑制することができ、レーザ光照射時にはレーザ光透過性に優れる。 According to the dicing sheet according to the present invention, it is possible to suppress the occurrence of blocking when the dicing sheet is unwound from the state of being wound up in a roll shape, and is excellent in laser light transmittance when irradiated with laser light.

本発明の一実施形態に係るダイシングシートの断面図である。It is sectional drawing of the dicing sheet which concerns on one Embodiment of this invention. 本発明の一実施形態に係るダイシングシートの使用例、具体的には積層構造体を示す断面図である。It is sectional drawing which shows the usage example of the dicing sheet which concerns on one Embodiment of this invention, specifically a laminated structure. 本発明の他の実施形態に係るダイシングシートの断面図である。It is sectional drawing of the dicing sheet which concerns on other embodiment of this invention. 実施例で作製したダイシングシートの平面図である。It is a top view of the dicing sheet produced in the Example.

 以下、本発明の実施形態について説明する。
 図1は本発明の一実施形態に係るダイシングシートの断面図である。図1に示すように、本実施形態に係るダイシングシート1は、基材2と、基材2の第1の面側(図1中における上側)に積層された粘着剤層3と、粘着剤層3上に積層された剥離シート6とを備えて構成される。剥離シート6は、ダイシングシート1の使用時に剥離除去され、それまで粘着剤層3を保護するものである。ここで、基材2における粘着剤層3側の面を「第1の面」、その反対側の面(図1中における下面)を「第2の面」という。
Hereinafter, embodiments of the present invention will be described.
FIG. 1 is a cross-sectional view of a dicing sheet according to an embodiment of the present invention. As shown in FIG. 1, the dicing sheet 1 according to the present embodiment includes a base material 2, a pressure-sensitive adhesive layer 3 laminated on the first surface side of the base material 2 (upper side in FIG. 1), and a pressure-sensitive adhesive. And a release sheet 6 laminated on the layer 3. The release sheet 6 is peeled and removed when the dicing sheet 1 is used, and protects the pressure-sensitive adhesive layer 3 until then. Here, the surface of the base material 2 on the pressure-sensitive adhesive layer 3 side is referred to as a “first surface”, and the opposite surface (the lower surface in FIG. 1) is referred to as a “second surface”.

 本実施形態に係るダイシングシート1は、一例として、ワークとしての半導体ウエハのダイシング加工時に、半導体ウエハを保持するために用いられるが、これに限定されるものではない。 The dicing sheet 1 according to the present embodiment is used, as an example, for holding a semiconductor wafer during dicing of a semiconductor wafer as a workpiece, but is not limited thereto.

 本実施形態に係るダイシングシート1は、通常、長尺に形成されてロール状に巻き取られ、ロール・トゥ・ロールで使用される。 The dicing sheet 1 according to the present embodiment is usually formed in a long shape, wound into a roll, and used in a roll-to-roll manner.

1.基材
 基材2の第2の面(以下「基材2の背面」という場合がある。)における算術平均粗さ(Ra1)は、0.2μm以上である。基材2の背面における、ダイシングシート1を130℃で2時間加熱し、室温まで冷却した後(以下、単に「加熱後」という場合がある。)の算術平均粗さ(Ra2)は、0.25μm以下である。なお、基材2の背面の算術平均粗さ(Ra1)は、130℃で2時間加熱する前の基材2の背面の算術平均粗さのことであり、以下「加熱前の算術平均粗さ(Ra1)」という場合がある。この加熱前の算術平均粗さ(Ra1)および加熱後の算術平均粗さ(Ra2)は、JIS B0601:2001に基づいて測定したものであり、測定方法の詳細は後述する試験例に示す通りである。
1. Base Material The arithmetic average roughness (Ra1) on the second surface of the base material 2 (hereinafter sometimes referred to as “the back surface of the base material 2”) is 0.2 μm or more. The arithmetic average roughness (Ra2) on the back surface of the substrate 2 after heating the dicing sheet 1 at 130 ° C. for 2 hours and cooling to room temperature (hereinafter sometimes simply referred to as “after heating”) is 0. 25 μm or less. In addition, the arithmetic mean roughness (Ra1) of the back surface of the base material 2 is the arithmetic average roughness of the back surface of the base material 2 before heating at 130 ° C. for 2 hours, and is hereinafter referred to as “arithmetic average roughness before heating”. (Ra1) ". The arithmetic average roughness (Ra1) before heating and the arithmetic average roughness (Ra2) after heating are measured based on JIS B0601: 2001, and the details of the measuring method are as shown in the test examples described later. is there.

 なお、巻き取ったロール状のダイシングシート1を繰り出す時は、加熱前であり、ステルスダイシングのレーザ光照射は、加熱後に行うものとする。 It should be noted that when the rolled dicing sheet 1 is unwound, it is before heating, and the laser beam irradiation of stealth dicing is performed after heating.

 基材2の背面の加熱前の算術平均粗さ(Ra1)が0.2μm以上であることにより、基材2の背面と、剥離シート6の粘着剤層3とは反対側の面とが密着し難。これにより、巻き取ったロール状のダイシングシート1を繰り出す時に、ブロッキングが発生し難い。したがって、ブロッキングに起因して、繰り出し不良が生じたり、基材2が巻き重なった剥離シート6に転写されてワークの貼付ができなくなったりすることを抑制することができる。 Arithmetic average roughness (Ra1) before heating of the back surface of the base material 2 is 0.2 μm or more, so that the back surface of the base material 2 and the surface opposite to the adhesive layer 3 of the release sheet 6 are in close contact with each other. Difficult. Thereby, blocking is hard to generate | occur | produce when unwinding the roll-shaped dicing sheet 1 wound up. Therefore, it is possible to suppress the occurrence of feeding failure due to blocking or the transfer of the workpiece 2 to the release sheet 6 on which the base material 2 is wound and the attachment of the workpiece to be impossible.

 上記の観点から、基材2の背面における加熱前の算術平均粗さ(Ra1)は、0.25μm以上であることが好ましく、特に0.30μm以上であることが好ましい。 From the above viewpoint, the arithmetic average roughness (Ra1) before heating on the back surface of the substrate 2 is preferably 0.25 μm or more, and particularly preferably 0.30 μm or more.

 ここで、基材2の背面における加熱前の算術平均粗さ(Ra1)の上限としては、1.0μm以下であることが好ましく、特に0.8μm以下であることが好ましく、さらには0.7μm以下であることが好ましい。加熱前の算術平均粗さ(Ra1)が1.0μmを超えると、上記した加熱後の算術平均粗さ(Ra2)を満たし難くなるおそれがある。
すなわち、基材41の背面における加熱前の算術平均粗さ(Ra1)は、0.25~1.0μmの範囲であることが好ましく、0.30~0.7μmの範囲であることがより好ましい。
Here, the upper limit of the arithmetic average roughness (Ra1) before heating on the back surface of the substrate 2 is preferably 1.0 μm or less, particularly preferably 0.8 μm or less, and more preferably 0.7 μm. The following is preferable. If the arithmetic average roughness (Ra1) before heating exceeds 1.0 μm, it may be difficult to satisfy the arithmetic average roughness (Ra2) after heating described above.
That is, the arithmetic average roughness (Ra1) before heating on the back surface of the substrate 41 is preferably in the range of 0.25 to 1.0 μm, and more preferably in the range of 0.30 to 0.7 μm. .

 一方、基材2の背面の上記条件による加熱後の算術平均粗さ(Ra2)が0.25μm以下であることにより、ダイシングシート1の加熱後、基材2の背面側からレーザ光を照射した時に、レーザ光が基材2の背面の凹凸で乱されることなくダイシングシート1を透過し、ワーク(半導体ウエハ)に効率良く到達し、レーザ光透過性に優れる。したがって、ステルスダイシングによるワークの分割性に優れる。 On the other hand, when the arithmetic average roughness (Ra2) after heating under the above conditions on the back surface of the base material 2 is 0.25 μm or less, the laser beam was irradiated from the back side of the base material 2 after the dicing sheet 1 was heated. Sometimes, the laser beam passes through the dicing sheet 1 without being disturbed by the unevenness on the back surface of the base material 2, efficiently reaches the workpiece (semiconductor wafer), and has excellent laser beam transparency. Therefore, it is excellent in the work division property by stealth dicing.

 上記の観点から、基材2の背面における加熱後の算術平均粗さ(Ra2)は、0.20μm以下であることが好ましく、特に0.10μm以下であることが好ましい。 From the above viewpoint, the arithmetic average roughness (Ra2) after heating on the back surface of the substrate 2 is preferably 0.20 μm or less, and particularly preferably 0.10 μm or less.

 ここで、基材2の背面における加熱後の算術平均粗さ(Ra2)の下限としては、加熱前の算術平均粗さ(Ra1)が満たされる限り、特に制限されない。ただし、通常は0.001μm以上、好ましくは0.01μm以上である。
すなわち、基材41の背面における加熱後の算術平均粗さ(Ra2)は、0.001~0.20μmの範囲であることが好ましく、0.01~0.10μmの範囲であることがより好ましい。
Here, the lower limit of the arithmetic average roughness (Ra2) after heating on the back surface of the substrate 2 is not particularly limited as long as the arithmetic average roughness (Ra1) before heating is satisfied. However, it is usually 0.001 μm or more, preferably 0.01 μm or more.
That is, the arithmetic average roughness (Ra2) after heating on the back surface of the substrate 41 is preferably in the range of 0.001 to 0.20 μm, and more preferably in the range of 0.01 to 0.10 μm. .

 また、基材2においては、基材2の背面における上記条件による加熱後の算術平均粗さ(Ra2)が、加熱前の算術平均粗さ(Ra1)より小さいことが好ましい。このように設定することにより、加熱前のブロッキング抑制効果および加熱後のレーザ光透過性の双方をより優れたものとすることができる。 Moreover, in the base material 2, it is preferable that the arithmetic average roughness (Ra2) after the heating by the said conditions in the back surface of the base material 2 is smaller than the arithmetic average roughness (Ra1) before a heating. By setting in this way, both the blocking suppression effect before heating and the laser beam transparency after heating can be made more excellent.

 基材2の背面における加熱前の算術平均粗さ(Ra1)を調整する方法としては、特に限定されないが、一般的には、基材2を構成する樹脂フィルムを製膜する際に用いるロール表面の表面粗さを変えることや、サンドブラスト加工、あるいは加熱により溶融してフラットになるフィラーの配合などによって調整することができる。 Although it does not specifically limit as a method of adjusting arithmetic mean roughness (Ra1) before the heating in the back surface of the base material 2, Generally, the roll surface used when forming the resin film which comprises the base material 2 The surface roughness can be changed, sandblasting, or blending of fillers that melt and become flat by heating can be adjusted.

 一方、基材2の背面における加熱後の算術平均粗さ(Ra2)を調整する方法としては、基材2を、融点が所定の範囲にある樹脂フィルム(樹脂系の材料を主材とするフィルム)から構成することが好ましく、特に、融点が所定の範囲にあるとともに、130℃における貯蔵弾性率が所定の範囲にある樹脂フィルムから構成することが好ましい。 On the other hand, as a method for adjusting the arithmetic average roughness (Ra2) after heating on the back surface of the base material 2, the base material 2 is a resin film having a melting point within a predetermined range (a film mainly composed of a resin-based material). In particular, it is preferable to form a resin film having a melting point within a predetermined range and a storage elastic modulus at 130 ° C. within a predetermined range.

 基材2の融点は、90~180℃であることが好ましく、特に100~160℃であることが好ましく、さらに110~150℃であることが好ましい。基材2の融点が上記の範囲にあることで、基材2の背面における加熱後の算術平均粗さ(Ra2)を上記の範囲に調整しやすい。基材2の融点が90℃未満であると、加熱中に基材2が完全に溶融してしまうおそれがある。一方、基材2の融点が180℃を超えると、基材2の背面における算術平均粗さが、130℃・2時間の加熱によっても変化しないおそれがある。なお、上記融点は、JIS K7121(ISO3146)に基づいて測定したものであり、測定方法の詳細は後述する試験例に示す通りである。 The melting point of the substrate 2 is preferably 90 to 180 ° C, particularly preferably 100 to 160 ° C, and more preferably 110 to 150 ° C. When the melting point of the base material 2 is in the above range, the arithmetic average roughness (Ra2) after heating on the back surface of the base material 2 can be easily adjusted to the above range. If the melting point of the substrate 2 is less than 90 ° C, the substrate 2 may be completely melted during heating. On the other hand, when the melting point of the base material 2 exceeds 180 ° C., the arithmetic average roughness on the back surface of the base material 2 may not be changed by heating at 130 ° C. for 2 hours. In addition, the said melting | fusing point was measured based on JISK7121 (ISO3146), and the detail of the measuring method is as showing to the test example mentioned later.

 基材2の融点を調整する方法に特に制限はないが、一般的には、主として、用いる樹脂材料の融点によって調整することができる。また、融点の異なる複数の樹脂材料を混合したり、複数のモノマーを共重合したりすることで、基材2任意の融点に調整することもできる。 Although there is no restriction | limiting in particular in the method of adjusting the melting | fusing point of the base material 2, Generally, it can adjust mainly by melting | fusing point of the resin material to be used. Further, the base material 2 can be adjusted to an arbitrary melting point by mixing a plurality of resin materials having different melting points or by copolymerizing a plurality of monomers.

 基材2の130℃における貯蔵弾性率は、1~100MPaであることが好ましく、特に2~80MPaであることが好ましく、さらに5~50MPaであることが好ましい。基材2の130℃における貯蔵弾性率が上記の範囲にあることで、基材2の背面における加熱後の算術平均粗さ(Ra2)を上記の範囲に調整しやすい。基材2の130℃における貯蔵弾性率が1MPa未満であると、加熱処理中に基材2が大きく変形してしまい、ワークを保持することができなくなるおそれがある。一方、基材2の130℃における貯蔵弾性率が100MPaを超えると、基材2の背面における算術平均粗さが、130℃・2時間の加熱によっても変化しないおそれがある。なお、上記貯蔵弾性率の測定方法は、後述する試験例に示す通りである。 The storage elastic modulus of the substrate 2 at 130 ° C. is preferably 1 to 100 MPa, particularly preferably 2 to 80 MPa, and further preferably 5 to 50 MPa. When the storage elastic modulus at 130 ° C. of the base material 2 is in the above range, the arithmetic average roughness (Ra2) after heating on the back surface of the base material 2 can be easily adjusted to the above range. If the storage elastic modulus at 130 ° C. of the base material 2 is less than 1 MPa, the base material 2 may be greatly deformed during the heat treatment, and the workpiece may not be held. On the other hand, when the storage elastic modulus at 130 ° C. of the substrate 2 exceeds 100 MPa, the arithmetic average roughness on the back surface of the substrate 2 may not be changed even by heating at 130 ° C. for 2 hours. In addition, the measuring method of the said storage elastic modulus is as showing to the test example mentioned later.

 基材2の130℃における貯蔵弾性率を調整する方法に、特に限定はないが、一般的には、主として、用いる樹脂材料の貯蔵弾性率によって調整することができる。また、一般的に、同じ化学構造であっても分子量が高いと貯蔵弾性率は高くなる傾向があり、架橋や狭い分子量分布によっても貯蔵弾性率が高くなる傾向がある。この傾向を踏まえて、基材2を任意の貯蔵弾性率に調整することができる。 The method for adjusting the storage elastic modulus of the substrate 2 at 130 ° C. is not particularly limited, but in general, it can be adjusted mainly by the storage elastic modulus of the resin material to be used. In general, even if the chemical structure is the same, if the molecular weight is high, the storage elastic modulus tends to increase, and the storage elastic modulus tends to increase due to cross-linking and narrow molecular weight distribution. Based on this tendency, the base material 2 can be adjusted to an arbitrary storage elastic modulus.

 ステルスダイシング等において波長1064nmのレーザ光を使用する場合、基材2の加熱後における波長1064nmの光線透過率は、40%以上であることが好ましく、特に50%以上であることが好ましく、さらに60%以上であることが好ましい。基材2の加熱後における波長1064nmの光線透過率が上記の範囲にあることで、ステルスダイシングによるワークの分割性に優れたものとなる。本実施形態では、基材2の背面における加熱後の算術平均粗さ(Ra2)が上記の範囲にあることにより、上記の光線透過率を実現することが可能となる。なお、基材2の加熱後における波長1064nmの光線透過率は高いほど好ましいが、実現可能な光線透過率としては、最大で、概ね99%程度である。 When laser light having a wavelength of 1064 nm is used in stealth dicing or the like, the light transmittance at a wavelength of 1064 nm after heating the substrate 2 is preferably 40% or more, particularly preferably 50% or more, and further 60 % Or more is preferable. Since the light transmittance at a wavelength of 1064 nm after the heating of the base material 2 is in the above range, the work can be easily divided by stealth dicing. In this embodiment, when the arithmetic mean roughness (Ra2) after heating on the back surface of the base material 2 is in the above range, the above light transmittance can be realized. The higher the light transmittance at a wavelength of 1064 nm after heating the substrate 2, the better, but the light transmittance that can be realized is about 99% at the maximum.

 基材2を構成する樹脂フィルムの具体例としては、低密度ポリエチレン(LDPE)フィルム、直鎖低密度ポリエチレン(LLDPE)フィルム、高密度ポリエチレン(HDPE)フィルム等のポリエチレンフィルム、ポリプロピレンフィルム、エチレン-プロピレン共重合体フィルム、ポリブテンフィルム、ポリブタジエンフィルム、ポリメチルペンテンフィルム、エチレン-ノルボルネン共重合体フィルム、ノルボルネン樹脂フィルム等のポリオレフィン系フィルム;エチレン-酢酸ビニル共重合体フィルム、エチレン-(メタ)アクリル酸共重合体フィルム、エチレン-(メタ)アクリル酸エステル共重合体フィルム等のエチレン系共重合フィルム;ポリ塩化ビニルフィルム、塩化ビニル共重合体フィルム等のポリ塩化ビニル系フィルム;ポリエチレンテレフタレートフィルム、ポリブチレンテレフタレートフィルム等のポリエステル系フィルム;ポリウレタンフィルム;ポリイミドフィルム;ポリスチレンフィルム;ポリカーボネートフィルム;フッ素樹脂フィルムなどが挙げられる。また、これらの架橋フィルム、アイオノマーフィルムのような変性フィルムも用いられる。さらに上記フィルムを複数積層した積層フィルムであってもよい。なお、本明細書における「(メタ)アクリル酸」は、アクリル酸およびメタクリル酸の両方を意味する。他の類似用語についても同様である。 Specific examples of the resin film constituting the substrate 2 include polyethylene films such as low density polyethylene (LDPE) film, linear low density polyethylene (LLDPE) film, and high density polyethylene (HDPE) film, polypropylene film, and ethylene-propylene. Polyolefin films such as copolymer film, polybutene film, polybutadiene film, polymethylpentene film, ethylene-norbornene copolymer film, norbornene resin film; ethylene-vinyl acetate copolymer film, ethylene- (meth) acrylic acid copolymer Polymer films, ethylene copolymer films such as ethylene- (meth) acrylate copolymer films; polyvinyl chloride films such as polyvinyl chloride films and vinyl chloride copolymer films Arm, polyethylene terephthalate film, a polyester film such as polyethylene terephthalate and polybutylene terephthalate film; polyurethane film; polyimide film; polystyrene films; polycarbonate films; and fluorine resin film. In addition, modified films such as these crosslinked films and ionomer films are also used. Furthermore, a laminated film in which a plurality of the above films are laminated may be used. In addition, “(meth) acrylic acid” in the present specification means both acrylic acid and methacrylic acid. The same applies to other similar terms.

 積層フィルムの場合、例えば、基材2の背面側に、加熱前後で算術平均粗さが変化するフィルムを配置し、基材2の粘着剤層3側に、耐熱性があって高温でも変形しないフィルムを配置することが好ましい。 In the case of a laminated film, for example, a film whose arithmetic average roughness changes before and after heating is disposed on the back side of the base material 2, and the adhesive layer 3 side of the base material 2 has heat resistance and does not deform even at high temperatures. It is preferable to arrange a film.

 上記の中でも、ポリオレフィン系フィルムが好ましく、特に、ポリエチレンフィルム、ポリプロピレンフィルムおよびエチレン-プロピレン共重合体フィルムが好ましく、さらにはエチレン-プロピレン共重合体フィルムが好ましい。これらの樹脂フィルムによれば、前述した物性を満たし易く、特に、エチレン-プロピレン共重合体フィルムの場合には、エチレンモノマーとプロピレンモノマーとの共重合比を調整することにより、前述した物性を満たし易い。また、これらの樹脂フィルムは、ワーク貼付性やチップ剥離性の観点からも好ましい。 Among the above, polyolefin film is preferable, polyethylene film, polypropylene film and ethylene-propylene copolymer film are particularly preferable, and ethylene-propylene copolymer film is more preferable. According to these resin films, the above-described physical properties are easily satisfied. In particular, in the case of an ethylene-propylene copolymer film, the above-described physical properties are satisfied by adjusting the copolymerization ratio of the ethylene monomer and the propylene monomer. easy. Moreover, these resin films are preferable also from a viewpoint of workpiece sticking property or chip peelability.

 上記樹脂フィルムは、その表面に積層される粘着剤層3との密着性を向上させる目的で、所望により、片面または両面に、酸化法や凹凸化法などによる表面処理、あるいはプライマー処理を施すことができる。上記酸化法としては、例えば、コロナ放電処理、プラズマ放電処理、クロム酸化処理(湿式)、火炎処理、熱風処理、オゾン、紫外線照射処理などが挙げられ、また、凹凸化法としては、例えばサンドブラスト法、溶射処理法などが挙げられる。 For the purpose of improving the adhesiveness with the pressure-sensitive adhesive layer 3 laminated on the surface, the resin film is subjected to surface treatment by an oxidation method, a concavo-convex method, or a primer treatment on one side or both sides as desired. Can do. Examples of the oxidation method include corona discharge treatment, plasma discharge treatment, chromium oxidation treatment (wet), flame treatment, hot air treatment, ozone, ultraviolet irradiation treatment, and the like. And a thermal spraying method.

 なお、基材2は、上記樹脂フィルム中に、着色剤、難燃剤、可塑剤、帯電防止剤、滑剤、フィラー等の各種添加剤を含有してもよい。 In addition, the base material 2 may contain various additives, such as a coloring agent, a flame retardant, a plasticizer, an antistatic agent, a lubricant, a filler, in the said resin film.

 基材2の厚さは、ダイシングシート1が使用される各工程において適切に機能できる限り、特に限定されないが、20~450μmであることが好ましく、特に25~400μmであることが好ましく、さらには50~350μmであることが好ましい。 The thickness of the substrate 2 is not particularly limited as long as it can function properly in each step in which the dicing sheet 1 is used, but is preferably 20 to 450 μm, more preferably 25 to 400 μm, It is preferably 50 to 350 μm.

2.粘着剤層
 本実施形態に係るダイシングシート1が備える粘着剤層3は、非エネルギー線硬化性粘着剤から構成されてもよいし、エネルギー線硬化性粘着剤から構成されてもよい。非エネルギー線硬化性粘着剤としては、所望の粘着力および再剥離性を有するものが好ましく、例えば、アクリル系粘着剤、ゴム系粘着剤、シリコーン系粘着剤、ウレタン系粘着剤、ポリエステル系粘着剤、ポリビニルエーテル系粘着剤等を使用することができる。これらの中でも、ダイシング工程等において、ワークまたは加工物の脱落を効果的に抑制することができるアクリル系粘着剤が好ましい。
2. Pressure-sensitive adhesive layer The pressure-sensitive adhesive layer 3 included in the dicing sheet 1 according to the present embodiment may be made of a non-energy ray-curable pressure-sensitive adhesive or may be made of an energy-ray-curable pressure-sensitive adhesive. As the non-energy ray curable pressure-sensitive adhesive, those having desired adhesive strength and removability are preferable. For example, acrylic pressure-sensitive adhesive, rubber-based pressure-sensitive adhesive, silicone-based pressure-sensitive adhesive, urethane-based pressure-sensitive adhesive, and polyester-based pressure-sensitive adhesive Polyvinyl ether-based pressure-sensitive adhesives can be used. Among these, in the dicing process or the like, an acrylic pressure-sensitive adhesive that can effectively prevent the workpiece or workpiece from falling off is preferable.

 一方、エネルギー線硬化性粘着剤は、エネルギー線照射により粘着力が低下するため、ワークまたは加工物とダイシングシート1とを分離させたいときに、エネルギー線照射することにより、容易に分離させることができる。 On the other hand, since the adhesive strength of the energy ray curable pressure-sensitive adhesive is reduced by energy ray irradiation, when the workpiece or workpiece and the dicing sheet 1 are to be separated, they can be easily separated by irradiation with energy rays. it can.

 粘着剤層3を構成するエネルギー線硬化性粘着剤は、エネルギー線硬化性を有するポリマーを主成分とするものであってもよいし、エネルギー線硬化性を有しないポリマーと、エネルギー線硬化性の多官能モノマー、および/または、オリゴマーとの混合物を主成分とするものであってもよい。 The energy ray-curable pressure-sensitive adhesive constituting the pressure-sensitive adhesive layer 3 may be mainly composed of a polymer having energy ray-curability, or a polymer having no energy ray-curability and an energy ray-curable property. The main component may be a polyfunctional monomer and / or a mixture with an oligomer.

 エネルギー線硬化性粘着剤が、エネルギー線硬化性を有するポリマーを主成分とする場合について、以下に説明する。 The case where the energy ray-curable pressure-sensitive adhesive is mainly composed of a polymer having energy ray-curability will be described below.

 エネルギー線硬化性を有するポリマーは、側鎖にエネルギー線硬化性を有する官能基(エネルギー線硬化性基)が導入された(メタ)アクリル酸エステル(共)重合体(A)(以下「エネルギー線硬化型重合体(A)」という場合がある。)であることが好ましい。このエネルギー線硬化型重合体(A)は、官能基含有モノマー単位を有する(メタ)アクリル系共重合体(a1)と、その官能基に結合する置換基を有する不飽和基含有化合物(a2)とを反応させて得られるものであることが好ましい。 The polymer having energy ray curability is a (meth) acrylic acid ester (co) polymer (A) (hereinafter referred to as “energy ray”) in which a functional group having energy ray curability (energy ray curable group) is introduced into the side chain. It may be referred to as “curable polymer (A)”). This energy ray curable polymer (A) includes a (meth) acrylic copolymer (a1) having a functional group-containing monomer unit, and an unsaturated group-containing compound (a2) having a substituent bonded to the functional group. It is preferable that it is obtained by making it react.

 アクリル系共重合体(a1)は、官能基含有モノマーから導かれる構成単位と、(メタ)アクリル酸エステルモノマー、または、その誘導体から導かれる構成単位とからなる。 The acrylic copolymer (a1) is composed of a structural unit derived from a functional group-containing monomer and a structural unit derived from a (meth) acrylic acid ester monomer or a derivative thereof.

 アクリル系共重合体(a1)の構成単位としての官能基含有モノマーは、重合性の二重結合と、ヒドロキシル基、アミノ基、置換アミノ基、エポキシ基等の官能基とを分子内に有するモノマーであることが好ましい。 The functional group-containing monomer as a constituent unit of the acrylic copolymer (a1) is a monomer having a polymerizable double bond and a functional group such as a hydroxyl group, an amino group, a substituted amino group, or an epoxy group in the molecule. It is preferable that

 上記官能基含有モノマーのさらに具体的な例としては、2-ヒドロキシエチル(メタ)アクリレート、2-ヒドロキシプロピル(メタ)アクリレート、3-ヒドロキシプロピル(メタ)アクリレート、4-ヒドロキシブチル(メタ)アクリレート等が挙げられ、これらを単独または2種以上を組み合わせて用いられる。 More specific examples of the functional group-containing monomer include 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 3-hydroxypropyl (meth) acrylate, 4-hydroxybutyl (meth) acrylate, and the like. These may be used alone or in combination of two or more.

 アクリル系共重合体(a1)を構成する(メタ)アクリル酸エステルモノマーとしては、アルキル基の炭素数が1~20であるアルキル(メタ)アクリレート、シクロアルキル(メタ)アクリレート、ベンジル(メタ)アクリレートが用いられる。これらの中でも、特に好ましくは、アルキル基の炭素数が1~18であるアルキル(メタ)アクリレート、例えば、メチル(メタ)アクリレート、エチル(メタ)アクリレート、プロピル(メタ)アクリレート、n-ブチル(メタ)アクリレート、2-エチルヘキシル(メタ)アクリレート等が用いられる。 Examples of the (meth) acrylic acid ester monomer constituting the acrylic copolymer (a1) include alkyl (meth) acrylates having 1 to 20 carbon atoms in the alkyl group, cycloalkyl (meth) acrylates, and benzyl (meth) acrylates. Is used. Among these, particularly preferred are alkyl (meth) acrylates having an alkyl group having 1 to 18 carbon atoms, such as methyl (meth) acrylate, ethyl (meth) acrylate, propyl (meth) acrylate, n-butyl (meth) ) Acrylate, 2-ethylhexyl (meth) acrylate and the like are used.

 アクリル系共重合体(a1)は、上記官能基含有モノマーから導かれる構成単位を、アクリル系共重合体(a1)の総質量に対して、通常3~100質量%、好ましくは4~80%、より好ましくは5~40質量%の割合で含有し、(メタ)アクリル酸エステルモノマー、または、その誘導体から導かれる構成単位を、アクリル系共重合体(a1)の総質量に対して、通常0~97質量%、好ましくは60~95質量%の割合で含有してなる。 In the acrylic copolymer (a1), the structural unit derived from the functional group-containing monomer is usually 3 to 100% by mass, preferably 4 to 80%, based on the total mass of the acrylic copolymer (a1). More preferably, it is contained in a proportion of 5 to 40% by mass, and the structural unit derived from the (meth) acrylic acid ester monomer or derivative thereof is usually based on the total mass of the acrylic copolymer (a1). It is contained in a proportion of 0 to 97% by mass, preferably 60 to 95% by mass.

 アクリル系共重合体(a1)は、上記のような官能基含有モノマーと、(メタ)アクリル酸エステルモノマーまたはその誘導体とを常法で共重合することにより得られるが、これらモノマーの他にもジメチルアクリルアミド、蟻酸ビニル、酢酸ビニル、スチレン等が共重合されてもよい。 The acrylic copolymer (a1) can be obtained by copolymerizing a functional group-containing monomer as described above with a (meth) acrylic acid ester monomer or a derivative thereof in a conventional manner. Dimethylacrylamide, vinyl formate, vinyl acetate, styrene and the like may be copolymerized.

 上記官能基含有モノマー単位を有するアクリル系共重合体(a1)を、その官能基に結合する置換基を有する不飽和基含有化合物(a2)と反応させることにより、エネルギー線硬化型重合体(A)が得られる。 By reacting the acrylic copolymer (a1) having the functional group-containing monomer unit with an unsaturated group-containing compound (a2) having a substituent bonded to the functional group, an energy beam curable polymer (A ) Is obtained.

 不飽和基含有化合物(a2)が有する置換基は、アクリル系共重合体(a1)が有する官能基含有モノマー単位の官能基の種類に応じて、適宜選択することができる。例えば、官能基がヒドロキシル基、アミノ基または置換アミノ基の場合、置換基としてはイソシアネート基またはエポキシ基が好ましく、官能基がエポキシ基の場合、置換基としてはアミノ基、カルボキシル基またはアジリジニル基が好ましい。 The substituent of the unsaturated group-containing compound (a2) can be appropriately selected according to the type of functional group of the functional group-containing monomer unit of the acrylic copolymer (a1). For example, when the functional group is a hydroxyl group, an amino group or a substituted amino group, the substituent is preferably an isocyanate group or an epoxy group, and when the functional group is an epoxy group, the substituent is an amino group, a carboxyl group or an aziridinyl group. preferable.

 また、不飽和基含有化合物(a2)には、エネルギー線重合性の炭素-炭素二重結合が、1分子毎に1~5個、好ましくは1~2個含まれている。このような不飽和基含有化合物(a2)の具体例としては、例えば、2-メタクリロイルオキシエチルイソシアネート、メタ-イソプロペニル-α,α-ジメチルベンジルイソシアネート、メタクリロイルイソシアネート、アリルイソシアネート、1,1-(ビスアクリロイルオキシメチル)エチルイソシアネート;ジイソシアネート化合物またはポリイソシアネート化合物と、ヒドロキシエチル(メタ)アクリレートとの反応により得られるアクリロイルモノイソシアネート化合物;ジイソシアネート化合物またはポリイソシアネート化合物と、ポリオール化合物と、ヒドロキシエチル(メタ)アクリレートとの反応により得られるアクリロイルモノイソシアネート化合物;グリシジル(メタ)アクリレート;(メタ)アクリル酸、2-(1-アジリジニル)エチル(メタ)アクリレート、2-ビニル-2-オキサゾリン、2-イソプロペニル-2-オキサゾリン等が挙げられる。 Further, the unsaturated group-containing compound (a2) contains 1 to 5, preferably 1 to 2, energy-polymerizable carbon-carbon double bonds per molecule. Specific examples of such unsaturated group-containing compound (a2) include, for example, 2-methacryloyloxyethyl isocyanate, meta-isopropenyl-α, α-dimethylbenzyl isocyanate, methacryloyl isocyanate, allyl isocyanate, 1,1- ( Bisacryloyloxymethyl) ethyl isocyanate; acryloyl monoisocyanate compound obtained by reaction of diisocyanate compound or polyisocyanate compound with hydroxyethyl (meth) acrylate; diisocyanate compound or polyisocyanate compound, polyol compound, and hydroxyethyl (meth) Acryloyl monoisocyanate compound obtained by reaction with acrylate; glycidyl (meth) acrylate; (meth) acrylic acid, 2- (1 -Aziridinyl) ethyl (meth) acrylate, 2-vinyl-2-oxazoline, 2-isopropenyl-2-oxazoline and the like.

 不飽和基含有化合物(a2)は、上記アクリル系共重合体(a1)の官能基含有モノマー100当量当たりで、通常10~100当量、好ましくは20~95当量の割合で用いられる。 The unsaturated group-containing compound (a2) is usually used in a ratio of 10 to 100 equivalents, preferably 20 to 95 equivalents per 100 equivalents of the functional group-containing monomer of the acrylic copolymer (a1).

 アクリル系共重合体(a1)と不飽和基含有化合物(a2)との反応においては、官能基と置換基との組合せに応じて、反応の温度、圧力、溶媒、時間、触媒の有無、触媒の種類を適宜選択することができる。これにより、アクリル系共重合体(a1)中に存在する官能基と、不飽和基含有化合物(a2)中の置換基とが反応し、不飽和基がアクリル系共重合体(a1)中の側鎖に導入され、エネルギー線硬化型重合体(A)が得られる。 In the reaction between the acrylic copolymer (a1) and the unsaturated group-containing compound (a2), depending on the combination of the functional group and the substituent, the reaction temperature, pressure, solvent, time, presence of catalyst, catalyst Can be selected as appropriate. As a result, the functional group present in the acrylic copolymer (a1) reacts with the substituent in the unsaturated group-containing compound (a2), so that the unsaturated group is contained in the acrylic copolymer (a1). It introduce | transduces into a side chain and an energy-beam curable polymer (A) is obtained.

 このようにして得られるエネルギー線硬化型重合体(A)の重量平均分子量は、1万以上であるのが好ましく、特に15万~150万であるのが好ましく、さらに20万~100万であるのが好ましい。なお、本明細書における重量平均分子量(Mw)とは、ゲルパーミエーションクロマトグラフィー法(GPC法)により測定したポリスチレン換算の値である。 The weight average molecular weight of the energy ray curable polymer (A) thus obtained is preferably 10,000 or more, particularly preferably 150,000 to 1,500,000, and more preferably 200,000 to 1,000,000. Is preferred. In addition, the weight average molecular weight (Mw) in this specification is the value of polystyrene conversion measured by the gel permeation chromatography method (GPC method).

 エネルギー線硬化性粘着剤が、エネルギー線硬化性を有するポリマーを主成分とする場合であっても、エネルギー線硬化性粘着剤は、さらに、エネルギー線硬化性のモノマーおよび/またはオリゴマー(B)を含有してもよい。 Even when the energy ray-curable pressure-sensitive adhesive has a polymer having energy ray-curability as a main component, the energy ray-curable pressure-sensitive adhesive further contains an energy ray-curable monomer and / or oligomer (B). You may contain.

 エネルギー線硬化性のモノマーおよび/またはオリゴマー(B)としては、例えば、多価アルコールと(メタ)アクリル酸とのエステル等を使用することができる。 As the energy ray-curable monomer and / or oligomer (B), for example, an ester of a polyhydric alcohol and (meth) acrylic acid or the like can be used.

 かかるエネルギー線硬化性のモノマーおよび/またはオリゴマー(B)としては、例えば、シクロヘキシル(メタ)アクリレート、イソボルニル(メタ)アクリレート等の単官能性アクリル酸エステル類、トリメチロールプロパントリ(メタ)アクリレート、ペンタエリスリトールトリ(メタ)アクリレート、ペンタエリスリトールテトラ(メタ)アクリレート、ジペンタエリスリトールヘキサ(メタ)アクリレート、1,4-ブタンジオールジ(メタ)アクリレート、1,6-ヘキサンジオールジ(メタ)アクリレート、ポリエチレングリコールジ(メタ)アクリレート、ジメチロールトリシクロデカンジ(メタ)アクリレート等の多官能性アクリル酸エステル類、ポリエステルオリゴ(メタ)アクリレート、ポリウレタンオリゴ(メタ)アクリレート等が挙げられる。 Examples of the energy ray-curable monomer and / or oligomer (B) include monofunctional acrylic acid esters such as cyclohexyl (meth) acrylate and isobornyl (meth) acrylate, trimethylolpropane tri (meth) acrylate, penta Erythritol tri (meth) acrylate, pentaerythritol tetra (meth) acrylate, dipentaerythritol hexa (meth) acrylate, 1,4-butanediol di (meth) acrylate, 1,6-hexanediol di (meth) acrylate, polyethylene glycol Polyfunctional acrylic esters such as di (meth) acrylate and dimethyloltricyclodecane di (meth) acrylate, polyester oligo (meth) acrylate, polyurethane oligo (meta Acrylate, and the like.

 エネルギー線硬化性のモノマーおよび/またはオリゴマー(B)を配合する場合、エネルギー線硬化性粘着剤中におけるエネルギー線硬化性のモノマーおよび/またはオリゴマー(B)の含有量は、エネルギー線硬化性粘着剤の総質量に対して、5~80質量%であることが好ましく、特に20~60質量%であることが好ましい。 When the energy ray curable monomer and / or oligomer (B) is blended, the content of the energy ray curable monomer and / or oligomer (B) in the energy ray curable adhesive is determined by the energy ray curable pressure sensitive adhesive. The total mass is preferably 5 to 80% by mass, more preferably 20 to 60% by mass.

 ここで、エネルギー線硬化性樹脂組成物を硬化させるためのエネルギー線として紫外線を用いる場合には、光重合開始剤(C)を添加することが好ましく、この光重合開始剤(C)の使用により、重合硬化時間および光線照射量を少なくすることができる。 Here, when using ultraviolet rays as an energy ray for curing the energy ray curable resin composition, it is preferable to add a photopolymerization initiator (C), and by using this photopolymerization initiator (C). The polymerization curing time and the amount of light irradiation can be reduced.

 光重合開始剤(C)としては、具体的には、ベンゾフェノン、アセトフェノン、ベンゾイン、ベンゾインメチルエーテル、ベンゾインエチルエーテル、ベンゾインイソプロピルエーテル、ベンゾインイソブチルエーテル、ベンゾイン安息香酸、ベンゾイン安息香酸メチル、ベンゾインジメチルケタール、2,4-ジエチルチオキサンソン、1-ヒドロキシシクロヘキシルフェニルケトン、ベンジルジフェニルサルファイド、テトラメチルチウラムモノサルファイド、アゾビスイソブチロニトリル、ベンジル、ジベンジル、ジアセチル、β-クロールアンスラキノン、(2,4,6-トリメチルベンジルジフェニル)フォスフィンオキサイド、2-ベンゾチアゾール-N,N-ジエチルジチオカルバメート、オリゴ{2-ヒドロキシ-2-メチル-1-[4-(1-プロペニル)フェニル]プロパノン}、2,2-ジメトキシ-1,2-ジフェニルエタン-1-オンなどが挙げられる。これらは単独で用いてもよいし、2種以上を併用してもよい。 Specific examples of the photopolymerization initiator (C) include benzophenone, acetophenone, benzoin, benzoin methyl ether, benzoin ethyl ether, benzoin isopropyl ether, benzoin isobutyl ether, benzoin benzoic acid, benzoin methyl benzoate, benzoin dimethyl ketal, 2,4-diethylthioxanthone, 1-hydroxycyclohexyl phenyl ketone, benzyldiphenyl sulfide, tetramethylthiuram monosulfide, azobisisobutyronitrile, benzyl, dibenzyl, diacetyl, β-chloranthraquinone, (2,4 6-trimethylbenzyldiphenyl) phosphine oxide, 2-benzothiazole-N, N-diethyldithiocarbamate, oligo {2-hydroxy-2-me Le-1- [4- (1-propenyl) phenyl] propanone}, and 2,2-dimethoxy-1,2-and the like. These may be used alone or in combination of two or more.

 光重合開始剤(C)は、エネルギー線硬化型共重合体(A)(エネルギー線硬化性のモノマーおよび/またはオリゴマー(B)を配合する場合には、エネルギー線硬化型共重合体(A)、および、エネルギー線硬化性のモノマーおよび/またはオリゴマー(B)の合計量100質量部)100質量部に対して0.1~10質量部、特には0.5~6質量部の範囲の量で用いられることが好ましい。 The photopolymerization initiator (C) is energy beam curable copolymer (A) (when energy beam curable monomer and / or oligomer (B) is blended, energy beam curable copolymer (A). , And a total amount of energy ray-curable monomer and / or oligomer (B) of 100 parts by mass) in an amount of 0.1 to 10 parts by mass, in particular 0.5 to 6 parts by mass with respect to 100 parts by mass. Is preferably used.

 エネルギー線硬化性粘着剤においては、上記成分以外にも、適宜他の成分を配合してもよい。他の成分としては、例えば、エネルギー線硬化性を有しないポリマー成分またはオリゴマー成分(D)、架橋剤(E)等が挙げられる。 In the energy ray-curable pressure-sensitive adhesive, other components may be appropriately blended in addition to the above components. Examples of other components include a polymer component or oligomer component (D) that does not have energy beam curability, and a crosslinking agent (E).

 エネルギー線硬化性を有しないポリマー成分またはオリゴマー成分(D)としては、例えば、ポリアクリル酸エステル、ポリエステル、ポリウレタン、ポリカーボネート、ポリオレフィン等が挙げられ、重量平均分子量(Mw)が3000~250万のポリマーまたはオリゴマーが好ましい。 Examples of the polymer component or oligomer component (D) having no energy ray curability include polyacrylates, polyesters, polyurethanes, polycarbonates, polyolefins, etc., and polymers having a weight average molecular weight (Mw) of 3,000 to 2.5 million. Or an oligomer is preferable.

 架橋剤(E)としては、エネルギー線硬化型共重合体(A)等が有する官能基との反応性を有する多官能性化合物を用いることができる。このような多官能性化合物の例としては、例えば、イソシアナート化合物、エポキシ化合物、アミン化合物、メラミン化合物、アジリジン化合物、ヒドラジン化合物、アルデヒド化合物、オキサゾリン化合物、金属アルコキシド化合物、金属キレート化合物、金属塩、アンモニウム塩、反応性フェノール樹脂等を挙げることができる。 As the crosslinking agent (E), a polyfunctional compound having reactivity with the functional group of the energy beam curable copolymer (A) or the like can be used. Examples of such polyfunctional compounds include, for example, isocyanate compounds, epoxy compounds, amine compounds, melamine compounds, aziridine compounds, hydrazine compounds, aldehyde compounds, oxazoline compounds, metal alkoxide compounds, metal chelate compounds, metal salts, Examples thereof include ammonium salts and reactive phenol resins.

 これら他の成分(D),(E)をエネルギー線硬化性粘着剤に配合することにより、粘着剤層3の硬化前における粘着性および剥離性、硬化後の強度、他の層との接着性、保存安定性などを改善し得る。これら他の成分の配合量は特に限定されず、エネルギー線硬化型共重合体(A)100質量部に対して0~40質量部の範囲で適宜決定される。 By blending these other components (D) and (E) into the energy ray-curable pressure-sensitive adhesive, the pressure-sensitive adhesive layer 3 is hardened and peelable before curing, strength after curing, and adhesion to other layers. , Storage stability and the like can be improved. The blending amount of these other components is not particularly limited, and is appropriately determined in the range of 0 to 40 parts by mass with respect to 100 parts by mass of the energy beam curable copolymer (A).

 次に、エネルギー線硬化性粘着剤が、エネルギー線硬化性を有しないポリマー成分とエネルギー線硬化性の多官能モノマーおよび/またはオリゴマーとの混合物を主成分とする場合について、以下に説明する。 Next, the case where the energy ray-curable adhesive is mainly composed of a mixture of a polymer component having no energy ray curability and an energy ray-curable polyfunctional monomer and / or oligomer will be described below.

 エネルギー線硬化性を有しないポリマー成分としては、例えば、前述したアクリル系共重合体(a1)と同様の成分が使用できる。エネルギー線硬化性樹脂組成物中におけるエネルギー線硬化性を有しないポリマー成分の含有量は、エネルギー線硬化性樹脂組成物の総質量に対して、20~99.9質量%であることが好ましく、特に30~80質量%であることが好ましい。 As the polymer component having no energy beam curability, for example, the same components as those of the acrylic copolymer (a1) described above can be used. The content of the polymer component having no energy beam curability in the energy beam curable resin composition is preferably 20 to 99.9% by mass with respect to the total mass of the energy beam curable resin composition, In particular, it is preferably 30 to 80% by mass.

 エネルギー線硬化性の多官能モノマーおよび/またはオリゴマーとしては、前述の成分(B)と同じものが選択される。エネルギー線硬化性を有しないポリマー成分とエネルギー線硬化性の多官能モノマーおよび/またはオリゴマーとの配合比は、ポリマー成分100質量部に対して、多官能モノマーおよび/またはオリゴマー10~150質量部であるのが好ましく、特に25~100質量部であるのが好ましい。 As the energy ray-curable polyfunctional monomer and / or oligomer, the same one as the above-mentioned component (B) is selected. The blending ratio of the polymer component having no energy ray curability and the energy ray curable polyfunctional monomer and / or oligomer is 10 to 150 parts by mass of the polyfunctional monomer and / or oligomer with respect to 100 parts by mass of the polymer component. The amount is preferably 25 to 100 parts by mass.

 この場合においても、上記と同様に、光重合開始剤(C)や架橋剤(E)を適宜配合することができる。 Also in this case, the photopolymerization initiator (C) and the crosslinking agent (E) can be appropriately blended as described above.

 粘着剤層3の厚さは、ダイシングシート1が使用される各工程において適切に機能できる限り、特に限定されない。具体的には、粘着剤層3の厚さは、1~50μmであることが好ましく、特に2~30μmであることが好ましく、さらには3~20μmであることが好ましい。 The thickness of the pressure-sensitive adhesive layer 3 is not particularly limited as long as it can function properly in each process in which the dicing sheet 1 is used. Specifically, the thickness of the pressure-sensitive adhesive layer 3 is preferably 1 to 50 μm, particularly preferably 2 to 30 μm, and further preferably 3 to 20 μm.

3.剥離シート
 本実施形態における剥離シート6は、ダイシングシート1が使用されるまでの間、粘着剤層3を保護する。本実施形態における剥離シート6は、粘着剤層3上に直接積層されているが、これに限定されるものではなく、粘着剤層3上に他の層(ダイボンディングフィルム等)が積層され、前記他の層上に剥離シート6が積層されてもよい。
3. Release Sheet The release sheet 6 in the present embodiment protects the pressure-sensitive adhesive layer 3 until the dicing sheet 1 is used. The release sheet 6 in the present embodiment is directly laminated on the pressure-sensitive adhesive layer 3, but is not limited to this, and other layers (such as a die bonding film) are laminated on the pressure-sensitive adhesive layer 3, A release sheet 6 may be laminated on the other layer.

 剥離シート6の構成は任意であり、プラスチックフィルムを剥離剤等により剥離処理したものが例示される。プラスチックフィルムの具体例としては、ポリエチレンテレフタレート、ポリブチレンテレフタレート、ポリエチレンナフタレート等のポリエステルフィルム、およびポリプロピレンやポリエチレン等のポリオレフィンフィルムが挙げられる。剥離剤としては、例えば、シリコーン系、フッ素系、長鎖アルキル系等を用いることができるが、これらの中で、安価で安定した性能が得られるシリコーン系が好ましい。剥離シート6の厚さについては、特に制限はないが、通常20~250μm程度である。 The configuration of the release sheet 6 is arbitrary, and examples include a plastic film that has been subjected to a release treatment with a release agent or the like. Specific examples of the plastic film include polyester films such as polyethylene terephthalate, polybutylene terephthalate, and polyethylene naphthalate, and polyolefin films such as polypropylene and polyethylene. As the release agent, for example, silicone-based, fluorine-based, long-chain alkyl-based, and the like can be used, and among these, a silicone-based material that can provide inexpensive and stable performance is preferable. The thickness of the release sheet 6 is not particularly limited, but is usually about 20 to 250 μm.

4.ダイシングシートの製造方法
 ダイシングシート1を製造するには、一例として、剥離シート6の剥離面に、粘着剤層3を構成する粘着剤と、所望によりさらに溶媒とを含有する粘着剤層用の塗布剤を塗布し乾燥させて粘着剤層3を形成する。その後、粘着剤層3の露出面に基材2を圧着し、基材2、粘着剤層3および剥離シート6からなるダイシングシート1を得る。
4). Manufacturing method of dicing sheet In order to manufacture the dicing sheet 1, as an example, an application for the pressure-sensitive adhesive layer containing the pressure-sensitive adhesive constituting the pressure-sensitive adhesive layer 3 and optionally a solvent on the release surface of the release sheet 6. An adhesive is applied and dried to form the pressure-sensitive adhesive layer 3. Then, the base material 2 is crimped | bonded to the exposed surface of the adhesive layer 3, and the dicing sheet 1 which consists of the base material 2, the adhesive layer 3, and the peeling sheet 6 is obtained.

 本実施形態における粘着剤層3は、リングフレーム等の治具に貼付可能であることが好ましい。この場合、粘着剤層3がエネルギー線硬化性粘着剤からなるとき、エネルギー線硬化性粘着剤を硬化させないことが好ましい。これにより、リングフレーム等の治具に対する接着力を高く維持することができる。 It is preferable that the pressure-sensitive adhesive layer 3 in the present embodiment can be attached to a jig such as a ring frame. In this case, when the pressure-sensitive adhesive layer 3 is made of an energy beam-curable pressure-sensitive adhesive, it is preferable not to cure the energy beam-curable pressure-sensitive adhesive. Thereby, the adhesive force with respect to jigs, such as a ring frame, can be maintained highly.

 基材2および粘着剤層3の積層体は、所望により、第1の剥離シートまたは第2の剥離シート側から、切断刃を入れるか、あるいはレーザ照射によるハーフカットを施し、所望の形状、例えばワーク(半導体ウエハ)に対応する円形等の形状に形成してもよい。この場合、ハーフカットにより生じた余分な部分は、適宜除去すればよい。 The laminated body of the base material 2 and the pressure-sensitive adhesive layer 3 may have a desired shape, for example, by inserting a cutting blade from the side of the first release sheet or the second release sheet or half-cutting by laser irradiation, as desired. You may form in circular shapes etc. corresponding to a workpiece | work (semiconductor wafer). In this case, an excess portion generated by the half cut may be removed as appropriate.

5.ダイシングシートの使用方法
 本実施形態に係るダイシングシート1を用いた一例として、ワークとしての半導体ウエハからチップを製造する方法を以下に説明する。
5. Method for Using Dicing Sheet As an example using the dicing sheet 1 according to the present embodiment, a method for manufacturing a chip from a semiconductor wafer as a workpiece will be described below.

 最初に、巻き取ったロール状のダイシングシート1を繰り出して、図2に示すように、ダイシングシート1の粘着剤層3を半導体ウエハ7およびリングフレーム8に貼付する。 First, the rolled-up dicing sheet 1 is unwound and the adhesive layer 3 of the dicing sheet 1 is attached to the semiconductor wafer 7 and the ring frame 8 as shown in FIG.

 本実施形態に係るダイシングシート1では、基材2の背面の加熱前の算術平均粗さ(Ra1)が0.2μm以上であることにより、上記繰り出し時にブロッキングが発生し難いため、繰り出し不良が生じたり、ワークの貼付ができなくなったりすることが抑制される。 In the dicing sheet 1 according to the present embodiment, since the arithmetic average roughness (Ra1) before heating of the back surface of the substrate 2 is 0.2 μm or more, blocking is unlikely to occur during the above-described feeding, so that feeding failure occurs. Or it becomes impossible to attach a workpiece.

 その後、伸長可能なダイシングシート1の粘着剤層3側の面に半導体ウエハ7が積層された構成を備える積層構造体(以下「積層構造体L」という場合がある。)を得る。図2に示される積層構造体Lはリングフレーム8をさらに備える。 Thereafter, a laminated structure having a configuration in which the semiconductor wafer 7 is laminated on the surface of the expandable dicing sheet 1 on the pressure-sensitive adhesive layer 3 side (hereinafter, sometimes referred to as “laminated structure L”) is obtained. The laminated structure L shown in FIG. 2 further includes a ring frame 8.

 ダイシングシート1には、加熱処理を施す。この際の加熱温度は、50~200℃、特に90~150℃であることが好ましく、加熱時間は、0.1~10時間、特に1~3時間であることが好ましい。本実施形態に係るダイシングシート1では、かかる加熱処理により、基材2の背面の算術平均粗さ(Ra2)が0.25μm以下になる。 The dicing sheet 1 is subjected to heat treatment. The heating temperature at this time is preferably 50 to 200 ° C., particularly 90 to 150 ° C., and the heating time is preferably 0.1 to 10 hours, particularly 1 to 3 hours. In the dicing sheet 1 according to the present embodiment, the arithmetic average roughness (Ra2) of the back surface of the substrate 2 is 0.25 μm or less by the heat treatment.

 次いで、積層構造体Lを、ステルスダイシング工程に付す。具体的には、積層構造体Lを、分割加工用レーザ照射装置に設置し、半導体ウエハ7の表面の位置を検出したのち、その半導体ウエハ7に対して、ダイシングシート1を介してレーザ光を照射し、半導体ウエハ7内に改質層を形成する。その後、ダイシングシート1を伸長させるエキスパンド工程を実施することにより、半導体ウエハ7に力(主面内方向の引張力)を付与する。その結果、ダイシングシート1に貼着する半導体ウエハ7は分割されて、チップが得られる。その後は、ピックアップ装置を用いて、ダイシングシート1からチップをピックアップする。 Next, the laminated structure L is subjected to a stealth dicing process. Specifically, the laminated structure L is installed in a split processing laser irradiation apparatus, the position of the surface of the semiconductor wafer 7 is detected, and then laser light is applied to the semiconductor wafer 7 via the dicing sheet 1. Irradiation forms a modified layer in the semiconductor wafer 7. Thereafter, an expanding process for extending the dicing sheet 1 is performed to apply a force (tensile force in the main surface direction) to the semiconductor wafer 7. As a result, the semiconductor wafer 7 adhered to the dicing sheet 1 is divided to obtain chips. Thereafter, a chip is picked up from the dicing sheet 1 using a pickup device.

 本実施形態に係るダイシングシート1では、基材2の背面の加熱後の算術平均粗さ(Ra2)が0.25μm以下であることにより、レーザ光透過性に優れるため、上記ステルスダイシング工程では、ステルスダイシングによるワークの分割性に優れる。 In the dicing sheet 1 according to the present embodiment, the arithmetic average roughness (Ra2) after heating of the back surface of the base material 2 is 0.25 μm or less, so that the laser light transmission is excellent, so in the stealth dicing step, Excellent work division by stealth dicing.

6.ダイシングシートの他の実施形態
 図3は、本発明の他の実施形態に係るダイシングシートの断面図である。図3に示すように、本実施形態に係るダイシングシート1Aは、基材2と、基材2の一方の面側(図1中、上側)に積層された粘着剤層3と、粘着剤層3における基材2とは反対側の周縁部に積層された治具用粘着剤層5と、粘着剤層3および治具用粘着剤層5上に積層された剥離シート6とを備えて構成される。治具用粘着剤層5は、ダイシングシート1をリングフレーム等の治具に接着するための層である。剥離シート6は、ダイシングシート1Aが使用されるまでの間、粘着剤層3および治具用粘着剤層5を保護する。すなわち、図1に示されるダイシングシート1に治具用粘着剤層5を加えたものが、図3に示されるダイシングシート1Aである。
6). Other Embodiments of Dicing Sheet FIG. 3 is a cross-sectional view of a dicing sheet according to another embodiment of the present invention. As shown in FIG. 3, the dicing sheet 1 </ b> A according to this embodiment includes a base material 2, a pressure-sensitive adhesive layer 3 laminated on one surface side (the upper side in FIG. 1), and a pressure-sensitive adhesive layer. 3 includes a jig pressure-sensitive adhesive layer 5 laminated on the peripheral edge opposite to the substrate 2, and a release sheet 6 laminated on the pressure-sensitive adhesive layer 3 and the jig pressure-sensitive adhesive layer 5. Is done. The adhesive layer 5 for jigs is a layer for bonding the dicing sheet 1 to a jig such as a ring frame. The release sheet 6 protects the pressure-sensitive adhesive layer 3 and the jig pressure-sensitive adhesive layer 5 until the dicing sheet 1A is used. That is, the dicing sheet 1A shown in FIG. 3 is obtained by adding the jig adhesive layer 5 to the dicing sheet 1 shown in FIG.

 治具用粘着剤層5を構成する粘着剤としては、所望の粘着力および再剥離性を有するものが好ましく、例えば、アクリル系粘着剤、ゴム系粘着剤、シリコーン系粘着剤、ウレタン系粘着剤、ポリエステル系粘着剤、ポリビニルエーテル系粘着剤等を使用することができる。これらの中でも、治具用粘着剤層5として、リングフレーム等の治具との密着性が高く、ダイシング工程等にてリングフレーム等からダイシングシート1Aが剥がれることを効果的に抑制することのできるアクリル系粘着剤を使用することが好ましい。なお、治具用粘着剤層5の厚さ方向の内部には、芯材としての基材が介在していてもよい。また、治具用粘着剤層5の粘着剤層3側には、基材が存在していてもよい。 As an adhesive which comprises the adhesive layer 5 for jig | tool, what has desired adhesive force and removability is preferable, for example, an acrylic adhesive, a rubber adhesive, a silicone adhesive, a urethane adhesive Polyester-based pressure-sensitive adhesives, polyvinyl ether-based pressure-sensitive adhesives, and the like can be used. Among these, the adhesive layer 5 for jigs has high adhesiveness with jigs such as a ring frame, and can effectively prevent the dicing sheet 1A from being peeled off from the ring frame or the like in a dicing process or the like. It is preferable to use an acrylic adhesive. In addition, the base material as a core material may interpose inside the thickness direction of the adhesive layer 5 for jig | tool. Moreover, the base material may exist in the adhesive layer 3 side of the adhesive layer 5 for jig | tool.

 治具用粘着剤層5の厚さは、リングフレーム等の治具に対する接着性の観点から、5~200μmであることが好ましく、特に10~100μmであることが好ましい。 The thickness of the pressure-sensitive adhesive layer 5 for jigs is preferably 5 to 200 μm, particularly preferably 10 to 100 μm, from the viewpoint of adhesion to a jig such as a ring frame.

 本実施形態に係るダイシングシート1Aにおける治具用粘着剤層5以外の各部材の材料および厚さ等は、前述したダイシングシート1の各部材の材料および厚さと同様である。 In the dicing sheet 1A according to the present embodiment, the material and thickness of each member other than the jig adhesive layer 5 are the same as the material and thickness of each member of the dicing sheet 1 described above.

 ダイシングシート1Aを製造する一例としては、まず、剥離シートの剥離面に、粘着剤層3を構成する粘着剤と、所望により、さらに溶媒とを含有する粘着剤層用の塗布剤を塗布し、乾燥させて粘着剤層3を形成する。その後、粘着剤層3の露出面に基材2を圧着し、基材2、粘着剤層3および剥離シートからなる積層体を得る。 As an example of manufacturing the dicing sheet 1A, first, a pressure-sensitive adhesive that constitutes the pressure-sensitive adhesive layer 3 and, if desired, a pressure-sensitive adhesive layer-containing coating agent are applied to the release surface of the release sheet. The pressure-sensitive adhesive layer 3 is formed by drying. Then, the base material 2 is crimped | bonded to the exposed surface of the adhesive layer 3, and the laminated body which consists of the base material 2, the adhesive layer 3, and a peeling sheet is obtained.

 ここで、粘着剤層3がエネルギー線硬化性粘着剤からなる場合には、この段階で粘着剤層3に対してエネルギー線を照射して、粘着剤層3を硬化させてもよいし、他の層を積層する場合には、他の層と積層した後に粘着剤層3を硬化させてもよい。また、他の層と積層した後に粘着剤層3を硬化させる場合、ダイシング工程前に粘着剤層3を硬化させてもよいし、ダイシング工程後に粘着剤層3を硬化させてもよい。 Here, when the pressure-sensitive adhesive layer 3 is made of an energy ray-curable pressure-sensitive adhesive, the pressure-sensitive adhesive layer 3 may be irradiated with energy rays at this stage to cure the pressure-sensitive adhesive layer 3. When laminating these layers, the pressure-sensitive adhesive layer 3 may be cured after laminating with other layers. When the pressure-sensitive adhesive layer 3 is cured after being laminated with another layer, the pressure-sensitive adhesive layer 3 may be cured before the dicing step, or the pressure-sensitive adhesive layer 3 may be cured after the dicing step.

 エネルギー線としては、通常、紫外線、電子線等が用いられる。エネルギー線の照射量は、エネルギー線の種類によって異なるが、例えば紫外線の場合には、光量で50~1000mJ/cmが好ましく、特に100~500mJ/cmが好ましい。また、電子線の場合には、10~1000krad程度が好ましい。 As energy rays, ultraviolet rays, electron beams, etc. are usually used. Irradiation of energy rays varies depending on the kind of energy rays, for example, in the case of ultraviolet rays, preferably 50 ~ 1000mJ / cm 2 in quantity, especially 100 ~ 500mJ / cm 2 preferably. In the case of an electron beam, about 10 to 1000 krad is preferable.

 基材2および粘着剤層3の積層体は、所望によりハーフカットし、所望の形状、例えばワーク(半導体ウエハ)に対応する円形等の形状に形成してもよい。この場合、ハーフカットにより生じた余分な部分は、適宜除去すればよい。 The laminate of the base material 2 and the pressure-sensitive adhesive layer 3 may be half-cut if desired, and formed into a desired shape, for example, a shape corresponding to a workpiece (semiconductor wafer). In this case, an excess portion generated by the half cut may be removed as appropriate.

 次いで、上記剥離シートを粘着剤層3から剥離し、露出した粘着剤層3の周縁部に、治具用粘着剤層5を形成する。治具用粘着剤層5も、上記粘着剤層3と同様の方法により、塗布して形成することができる。最後に、粘着剤層3および治具用粘着剤層5の露出面に、剥離シート6を積層し、ダイシングシート1Aを得る。 Next, the release sheet is peeled off from the pressure-sensitive adhesive layer 3, and a jig pressure-sensitive adhesive layer 5 is formed on the exposed peripheral edge of the pressure-sensitive adhesive layer 3. The jig pressure-sensitive adhesive layer 5 can also be formed by coating in the same manner as the pressure-sensitive adhesive layer 3. Finally, a release sheet 6 is laminated on the exposed surfaces of the pressure-sensitive adhesive layer 3 and the jig pressure-sensitive adhesive layer 5 to obtain a dicing sheet 1A.

 以上、ダイシングシート1Aの一製造方法を示したが、これに限定されるものではない。例えば、治具用粘着剤層5が基材を有するものである場合には、剥離シート上に治具用粘着剤層5用を構成する積層体を形成した後、治具に対応する環状等の形状にハーフカットし、これを上記粘着剤層3に積層するようにしてもよい。 As mentioned above, although one manufacturing method of dicing sheet 1A was shown, it is not limited to this. For example, when the jig pressure-sensitive adhesive layer 5 has a base material, after forming a laminate constituting the jig pressure-sensitive adhesive layer 5 on the release sheet, an annular shape corresponding to the jig, etc. It is also possible to make a half cut into the shape and laminate the adhesive layer 3 on the adhesive layer 3.

 以上説明した実施形態は、本発明の理解を容易にするために記載されたものであって、本発明を限定するために記載されたものではない。したがって、上記実施形態に開示された各要素は、本発明の技術的範囲に属する全ての設計変更や均等物をも含む趣旨である。 The embodiment described above is described for facilitating understanding of the present invention, and is not described for limiting the present invention. Therefore, each element disclosed in the above embodiment is intended to include all design changes and equivalents belonging to the technical scope of the present invention.

 例えば、ダイシングシート1,1Aにおける基材2と粘着剤層3との間には、他の層が介在していてもよい。また、ダイシングシート1,1Aにおける粘着剤層3と剥離シート6との間には、他の層が介在していてもよい。前記他の層としては、例えば、ダイボンディングフィルムが挙げられる。この場合、ダイシングシート1,1Aは、ダイシングダイボンディングシートとして使用することができる。 For example, another layer may be interposed between the base material 2 and the pressure-sensitive adhesive layer 3 in the dicing sheets 1 and 1A. Further, another layer may be interposed between the adhesive layer 3 and the release sheet 6 in the dicing sheets 1 and 1A. Examples of the other layer include a die bonding film. In this case, the dicing sheets 1 and 1A can be used as a dicing die bonding sheet.

また、本発明に係る保護膜形成用複合シートおいては、基材2の背面における加熱前の算術平均粗さ(Ra1)を0.51~0.65μm程度、130℃で2時間加熱した後の算術平均粗さ(Ra2)を0.08~0.22程度としたうえで、基材2の130℃における貯蔵弾性率を13~20MPa程度とすることで、耐ブロッキング性およびダイシング分割性により優れたものとなる。 In the composite sheet for forming a protective film according to the present invention, the arithmetic average roughness (Ra1) before heating on the back surface of the substrate 2 is about 0.51 to 0.65 μm and heated at 130 ° C. for 2 hours. In addition to setting the arithmetic average roughness (Ra2) of about 0.08 to 0.22, the storage elastic modulus of the base material 2 at 130 ° C. is set to about 13 to 20 MPa. It will be excellent.

 以下、実施例等により本発明をさらに具体的に説明するが、本発明の範囲はこれらの実施例等に限定されるものではない。 Hereinafter, the present invention will be described more specifically with reference to examples and the like, but the scope of the present invention is not limited to these examples and the like.

〔実施例1〕
 実施例1では、以下のようにして、図1,4に示すようなダイシングシート1を製造した。
[Example 1]
In Example 1, a dicing sheet 1 as shown in FIGS. 1 and 4 was manufactured as follows.

(1)積層体の作製
 次の(A)および(B)の成分を混合し、固形分濃度が30質量%となるようにメチルエチルケトンで希釈して、粘着剤層用塗布剤を調製した。
(A)粘着主剤:(メタ)アクリル酸エステル共重合体(ブチルアクリレート40質量部、2-エチルヘキシルアクリレート55質量部、および2-ヒドロキシルエチルアクリレート5質量部を共重合して得られた共重合体,重量平均分子量:60万)100質量部
(B)架橋剤:芳香族系ポリイソシアネート化合物(三井化学社製,タケネートD110N)10質量部
(1) Production of Laminate The following components (A) and (B) were mixed and diluted with methyl ethyl ketone so that the solid content concentration was 30% by mass to prepare an adhesive layer coating agent.
(A) Adhesive main agent: (meth) acrylic acid ester copolymer (copolymer obtained by copolymerizing 40 parts by mass of butyl acrylate, 55 parts by mass of 2-ethylhexyl acrylate, and 5 parts by mass of 2-hydroxylethyl acrylate) , Weight average molecular weight: 600,000) 100 parts by mass (B) Crosslinker: aromatic polyisocyanate compound (Mitsui Chemicals, Takenate D110N) 10 parts by mass

 次に、一方の面(基材の背面:基材の第2の面に該当)の加熱前の算術平均粗さ(Ra1)、および、加熱後(130℃・2時間)の算術平均粗さ(Ra2)、融点ならびに130℃における貯蔵弾性率を下記表1のように調整したエチレン-プロピレン共重合体フィルムを作製し、前記フィルムの他方の面にコロナ処理を施して、これを基材とした。なお、上記加熱前の算術平均粗さ(Ra1)は、基材の製膜時に背面側が巻き取られる金属ロール表面の算術表面粗さを変えることにより調整した。また、上記加熱後の算術平均粗さ(Ra2)は、基材のエチレン-プロピレン共重合体を構成するエチレンとプロピレンとの共重合比を変えることにより調整した。 Next, arithmetic average roughness (Ra1) before heating of one surface (back surface of the base material: corresponding to the second surface of the base material), and arithmetic average roughness after heating (130 ° C., 2 hours) (Ra2), an ethylene-propylene copolymer film having a melting point and a storage elastic modulus at 130 ° C. adjusted as shown in Table 1 below, and subjecting the other side of the film to corona treatment, did. In addition, the arithmetic mean roughness (Ra1) before the heating was adjusted by changing the arithmetic surface roughness of the surface of the metal roll on which the back side was wound up when the substrate was formed. The arithmetic average roughness (Ra2) after the heating was adjusted by changing the copolymerization ratio of ethylene and propylene constituting the ethylene-propylene copolymer of the base material.

 厚さ38μmのPETフィルムの片面にシリコーン系の剥離剤層が形成されてなる剥離シート(リンテック社製,SP-PET381031)を用意し、その剥離シートの剥離面上に、前述の粘着剤層用塗布剤を、最終的に得られる粘着剤層の厚さが10μmとなるように、ナイフコーターにて塗布し、乾燥させて、粘着剤層を形成した。その後、粘着剤層に前述した基材のコロナ処理面を重ねて両者を貼り合わせ、基材(図1における基材2)および粘着剤層(図1における粘着剤層3)と、剥離シートとからなる積層体を得た。この積層体は長尺であり、ロール状に巻き取って巻収体とした後、幅方向300mm(図4中、wで示す)に裁断した。 Prepare a release sheet (SP-PET 381031 manufactured by Lintec Co., Ltd.) with a silicone release agent layer formed on one side of a 38 μm thick PET film, and use the adhesive layer on the release surface of the release sheet. The coating agent was applied with a knife coater so that the finally obtained pressure-sensitive adhesive layer had a thickness of 10 μm, and dried to form a pressure-sensitive adhesive layer. Thereafter, the above-mentioned corona-treated surface of the base material is laminated on the pressure-sensitive adhesive layer and bonded together, and the base material (base material 2 in FIG. 1), the pressure-sensitive adhesive layer (pressure-sensitive adhesive layer 3 in FIG. 1), the release sheet, A laminate comprising: This laminated body was long, wound up in a roll shape to obtain a rolled body, and then cut into a width direction of 300 mm (indicated by w 1 in FIG. 4).

(2)ダイシングシートの作製
 上記(1)で得られた積層体に対し、上記基材側から、基材および粘着剤層の積層体を切断するようにハーフカットを施した。具体的には、図4に示すように、円形(直径d:270mm;図4中の符号401;円形のダイシングシート本体)を形成するとともに、その円形から外側に20mmの間隔(図4中、wで示す)を有する円弧(図4中の符号402)を形成した。また、隣り合う円形同士の間には、積層体の幅方向端部と平行する2本の直線(図4中の符号403)を形成し、前記直線にて隣り合う上記円弧を連結した。
(2) Production of dicing sheet The laminate obtained in the above (1) was half-cut so as to cut the laminate of the substrate and the pressure-sensitive adhesive layer from the substrate side. Specifically, as shown in FIG. 4, a circular shape (diameter d 1 : 270 mm; reference numeral 401 in FIG. 4; circular dicing sheet body) is formed, and an interval of 20 mm from the circular shape to the outside (in FIG. 4). , Indicated by w 2 ) was formed (reference numeral 402 in FIG. 4). In addition, two straight lines (reference numeral 403 in FIG. 4) parallel to the end portions in the width direction of the stacked body were formed between the adjacent circles, and the adjacent arcs were connected by the straight lines.

 その後、上記円形のダイシングシート本体と上記円弧との間の部分および上記2本の直線で挟まれた部分を除去し、図1,4に示すダイシングシートを得た。 Thereafter, the part between the circular dicing sheet main body and the arc and the part sandwiched between the two straight lines were removed, and the dicing sheet shown in FIGS.

〔実施例2~5および比較例1~3〕
 基材の背面の加熱前の算術平均粗さ(Ra1)および加熱後の算術平均粗さ(Ra2)、融点および130℃における貯蔵弾性率を、下記表1に示すように変更した点以外は、実施例1と同様にして実施例2~5および比較例1~3のダイシングシートを製造した。
[Examples 2 to 5 and Comparative Examples 1 to 3]
The arithmetic average roughness (Ra1) before heating and the arithmetic average roughness (Ra2) after heating, the melting point and the storage elastic modulus at 130 ° C. on the back surface of the base material were changed as shown in Table 1 below. In the same manner as in Example 1, dicing sheets of Examples 2 to 5 and Comparative Examples 1 to 3 were produced.

〔試験例1〕<基材の算術平均粗さの測定>
 実施例および比較例で使用した基材の背面における加熱前の算術平均粗さ(Ra1:μm)および加熱後の算術平均粗さ(Ra2:μm)を、接触式表面粗さ計(ミツトヨ社製,SURFTEST SV-3000)を用いて、カットオフ値λcを0.8mm、評価長さLnを4mmとし、JIS B0601:2001に準拠して測定した。この結果を下記表1に示す。
[Test Example 1] <Measurement of arithmetic average roughness of substrate>
The arithmetic average roughness before heating (Ra1: μm) and the arithmetic average roughness after heating (Ra2: μm) on the back surface of the base material used in Examples and Comparative Examples were measured using a contact-type surface roughness meter (manufactured by Mitutoyo Corporation). , SURFTEST SV-3000), the cut-off value λc was 0.8 mm, the evaluation length Ln was 4 mm, and the measurement was performed according to JIS B0601: 2001. The results are shown in Table 1 below.

 ここで、加熱後の算術平均粗さ(Ra2)については、前記基材を備えた実施例および比較例のダイシングシートをリングフレームに固定した状態で、オーブン内において、大気雰囲気下、130℃で2時間加熱した後、放置して室温まで冷却した後の値を測定した。この加熱処理の際には、測定面(基材の背面)がオーブン内の内壁や底部に接触しないようにした。 Here, for the arithmetic average roughness (Ra2) after heating, the dicing sheets of the examples and comparative examples provided with the base material were fixed to a ring frame, and in an oven at 130 ° C. in an air atmosphere. After heating for 2 hours, the value after standing to cool to room temperature was measured. During the heat treatment, the measurement surface (the back surface of the base material) was not in contact with the inner wall or bottom of the oven.

〔試験例2〕<基材の融点の測定>
 実施例および比較例で使用した基材について、示差走査熱量計(ティー・エイ・インスツルメント社製,Q2000)を用いて、JIS K7121(ISO3146)に準拠して融解ピーク温度を求めた。具体的には、基材を23℃から200℃まで毎分10℃で加熱し、DSC曲線を描いた。得られた昇温時のDSC曲線から融解ピーク温度(℃)を求めた。この結果を下記表1に示す。
[Test Example 2] <Measurement of melting point of substrate>
About the base material used by the Example and the comparative example, melting | dissolving peak temperature was calculated | required based on JISK7121 (ISO3146) using the differential scanning calorimeter (TA Instruments company make, Q2000). Specifically, the substrate was heated from 23 ° C. to 200 ° C. at 10 ° C. per minute to draw a DSC curve. The melting peak temperature (° C.) was determined from the obtained DSC curve at the time of temperature increase. The results are shown in Table 1 below.

〔試験例3〕<基材の貯蔵弾性率の測定>
 実施例および比較例で使用した基材について、下記の装置および条件で130℃における貯蔵弾性率を測定した。この結果を下記表1に示す。
 測定装置:ティー・エイ・インスツルメント社製,動的弾性率測定装置「DMA Q800」
 試験開始温度:0℃
 試験終了温度:200℃
 昇温速度:3℃/分
 周波数:11Hz
 振幅:20μm
[Test Example 3] <Measurement of storage elastic modulus of substrate>
With respect to the base materials used in Examples and Comparative Examples, the storage elastic modulus at 130 ° C. was measured with the following apparatus and conditions. The results are shown in Table 1 below.
Measuring device: Dynamic instrument measurement device “DMA Q800” manufactured by TA Instruments
Test start temperature: 0 ° C
Test end temperature: 200 ° C
Temperature increase rate: 3 ° C / min Frequency: 11Hz
Amplitude: 20 μm

〔試験例4〕<光線透過率の測定>
 実施例および比較例で使用した基材を、試験例1に示したように130℃で2時間加熱した後、前記加熱後の基材について、紫外可視分光光度計(島津製作所社製,UV-3101PC,積分球不使用)を用いて、波長200~1200nmの光線透過率を測定し、波長1064nmの測定値を読み取った。この結果を下記表1に示す。
[Test Example 4] <Measurement of light transmittance>
As shown in Test Example 1, the base materials used in the examples and comparative examples were heated at 130 ° C. for 2 hours, and then the heated base materials were subjected to UV-visible spectrophotometer (manufactured by Shimadzu Corporation, UV- 3101PC (without integrating sphere)), the light transmittance at a wavelength of 200 to 1200 nm was measured, and the measured value at a wavelength of 1064 nm was read. The results are shown in Table 1 below.

〔試験例5〕<耐ブロッキング性評価>
 実施例および比較例で製造したダイシングシートを貼付装置(リンテック社製,RAD-2700 F/12)にセットし、ロール・トゥ・ロールで、70℃の環境下にて、シリコンウエハ(外径:8インチ,厚さ:100μm)およびリングフレーム(ステンレス製)にダイシングシート本体を貼付した。その際、10枚連続で貼付作業を行い、下記の基準に基づいて耐ブロッキング性を評価した。この結果を下記表1に示す。
 A:問題なく貼付することができた(ブロッキングの発生が全くなし)。
 B:貼付はできたが、基材と基材背面側の剥離シートとが一部密着し、ダイシングシートを繰り出す際に、粘着剤層から剥離シートが一部剥離していた。
 C:1枚でもダイシングシート本体が基材背面側の剥離シートに転写されたり、ダイシングシートの繰り出しできなかったりする等の貼付不良が発生した(ブロッキングの発生あり)。
[Test Example 5] <Evaluation of blocking resistance>
The dicing sheets produced in the examples and comparative examples were set in a sticking apparatus (RAD-2700 F / 12, manufactured by Lintec Corporation), and roll-to-roll in a 70 ° C. environment at a silicon wafer (outer diameter: The dicing sheet main body was affixed to 8 inches, thickness: 100 μm) and a ring frame (made of stainless steel). At that time, 10 sheets were continuously applied, and blocking resistance was evaluated based on the following criteria. The results are shown in Table 1 below.
A: It was possible to apply without any problem (no blocking occurred at all).
B: Although pasting was possible, a part of the base material and the release sheet on the back side of the base material were in close contact, and the release sheet was partly released from the adhesive layer when the dicing sheet was fed out.
C: Even with one sheet, the dicing sheet main body was transferred to the release sheet on the back side of the base material, or a sticking failure such that the dicing sheet could not be fed out occurred (blocking occurred).

〔試験例6〕<ダイシング分割性評価>
 実施例および比較例で製造したダイシングシートを貼付装置(リンテック社製,RAD-2700 F/12)にセットし、70℃の環境下にて、シリコンウエハ(外径:8インチ,厚さ:100μm)およびリングフレーム(ステンレス製)にダイシングシート本体を貼付した。その後、130℃で2時間加熱処理を行った。
[Test Example 6] <Dicing division property evaluation>
The dicing sheets produced in the examples and comparative examples were set in a sticking apparatus (RAD-2700 F / 12, manufactured by Lintec Corporation), and the silicon wafer (outer diameter: 8 inches, thickness: 100 μm) in an environment of 70 ° C. ) And a ring frame (made of stainless steel). Thereafter, heat treatment was performed at 130 ° C. for 2 hours.

 次いで、ダイシングシート上のシリコンウエハに対して、レーザーソー(ディスコ社製,DFL7360)を用いて、次の工程からなるステルスダイシングによる分割加工を行った。
(工程1)実施例および比較例のダイシングシートが貼付されたシリコンウエハおよびリングフレームを、基材背面側からレーザ光を照射できるように、レーザーソーの所定の位置に設置する。
(工程2)シリコンウエハの表面の位置の検出を行った後、レーザーソーのレーザ光の焦点位置を設定し、シリコンウエハに9mm×9mmのチップ体が形成されるように設定された切断予定ラインに沿って、レーザーソーから波長1064nmのレーザ光を、基材背面側から10回照射して、シリコンウエハ内に改質層を形成する。
(工程3)ダイシングシートが貼付されたシリコンウエハおよびリングフレームを、ダイセパレーター(ディスコ社製,DDS2300)に設置し、引き落とし速度100mm/秒、エキスパンド量10mmでエキスパンドを行う。
Next, the silicon wafer on the dicing sheet was subjected to division processing by stealth dicing consisting of the following steps using a laser saw (DFL 7360, manufactured by Disco Corporation).
(Step 1) The silicon wafer and the ring frame to which the dicing sheets of Examples and Comparative Examples are attached are placed at predetermined positions of the laser saw so that laser light can be irradiated from the back side of the substrate.
(Step 2) After detecting the position of the surface of the silicon wafer, the focal position of the laser beam of the laser saw is set, and the planned cutting line is set so that a 9 mm × 9 mm chip body is formed on the silicon wafer. Then, a laser beam having a wavelength of 1064 nm is irradiated from the laser saw 10 times from the back side of the substrate to form a modified layer in the silicon wafer.
(Step 3) The silicon wafer and the ring frame to which the dicing sheet is attached are placed on a die separator (DDS 2300, manufactured by Disco Corporation), and expanded at a pulling rate of 100 mm / second and an expanding amount of 10 mm.

 以上の工程により、内部に改質層が形成されたシリコンウエハの少なくとも一部が分割予定ラインに沿って分割され、複数のチップが得られた。そのときの分割率(=(実際に分割して得られたチップ数/分割を予定していたチップ数)×100)(%)に基づき、下記の基準に従ってダイシング分割性を評価した。この結果を下記表1に示す。
 A:チップ分割率100%(分割性優良)
 B:チップ分割率90%以上100%未満(許容される分割性を有する)
 C:チップ分割率80%以上90%未満(許容される分割性を有する)
 D:チップ分割率80%未満(許容される分割性を有しない)
Through the above-described steps, at least a part of the silicon wafer having the modified layer formed therein was divided along the line to be divided, and a plurality of chips were obtained. Based on the division ratio (= (number of chips actually obtained / number of chips planned to be divided) × 100) (%), the dicing division property was evaluated according to the following criteria. The results are shown in Table 1 below.
A: Chip division ratio 100% (excellent division)
B: Chip division ratio of 90% or more and less than 100% (having an acceptable division property)
C: Chip division rate of 80% or more and less than 90% (having an acceptable division property)
D: Chip division rate of less than 80% (does not have acceptable division)

Figure JPOXMLDOC01-appb-T000001
Figure JPOXMLDOC01-appb-T000001

 表1から分かるように、基材の背面における加熱前の算術平均粗さ(Ra1)が0.2μm以上であり、基材の背面における130℃で2時間加熱した後の算術平均粗さ(Ra2)が0.25μm以下である実施例のダイシングシートは、耐ブロッキング性に優れるとともに、ダイシング分割性にも優れるものであった。 As can be seen from Table 1, the arithmetic average roughness (Ra1) before heating on the back surface of the substrate is 0.2 μm or more, and the arithmetic average roughness (Ra2) after heating at 130 ° C. for 2 hours on the back surface of the substrate. ) Is 0.25 μm or less, the dicing sheet of the example was excellent in blocking resistance and also in dicing resolution.

 本発明に係るダイシングシートは、ステルスダイシングなど、基材を透過させるようにレーザ光を照射する工程を含む場合に好適に用いられる。 The dicing sheet according to the present invention is suitably used when it includes a step of irradiating a laser beam so as to transmit the substrate, such as stealth dicing.

1,1A…ダイシングシート
2…基材
3…粘着剤層
401…円形
402…円弧
403…直線
5…治具用粘着剤層
6…剥離シート
7…半導体ウエハ
8…リングフレーム
DESCRIPTION OF SYMBOLS 1,1A ... Dicing sheet 2 ... Base material 3 ... Adhesive layer 401 ... Circular 402 ... Arc 403 ... Straight line 5 ... Jig adhesive layer 6 ... Release sheet 7 ... Semiconductor wafer 8 ... Ring frame

Claims (7)

 基材と、
 前記基材の第1の面側に積層された粘着剤層と、
 前記粘着剤層の前記基材とは反対の面側に積層された剥離シートと
を備えたダイシングシートであって、
 前記基材の第2の面における算術平均粗さ(Ra1)は、0.2μm以上であり、
 前記基材の第2の面における、前記ダイシングシートを130℃で2時間加熱した後の算術平均粗さ(Ra2)は、0.25μm以下である
ことを特徴とするダイシングシート。
A substrate;
A pressure-sensitive adhesive layer laminated on the first surface side of the substrate;
A dicing sheet provided with a release sheet laminated on the side of the pressure-sensitive adhesive layer opposite to the base material,
The arithmetic average roughness (Ra1) on the second surface of the substrate is 0.2 μm or more,
The arithmetic average roughness (Ra2) of the second surface of the substrate after heating the dicing sheet at 130 ° C. for 2 hours is 0.25 μm or less.
 前記基材の第2の面における前記加熱後の算術平均粗さ(Ra2)は、前記算術平均粗さ(Ra1)より小さいことを特徴とする請求項1に記載のダイシングシート。 The dicing sheet according to claim 1, wherein the arithmetic average roughness (Ra2) after the heating on the second surface of the substrate is smaller than the arithmetic average roughness (Ra1).  前記基材の融点は、90~180℃であることを特徴とする請求項1または2に記載のダイシングシート。 The dicing sheet according to claim 1 or 2, wherein the base material has a melting point of 90 to 180 ° C.  前記基材の130℃における貯蔵弾性率は、1~100MPaであることを特徴とする請求項1~3のいずれか一項に記載のダイシングシート。 The dicing sheet according to any one of claims 1 to 3, wherein the substrate has a storage elastic modulus at 130 ° C of 1 to 100 MPa.  前記基材の前記加熱後における波長1064nmの光線透過率は、40%以上であることを特徴とする請求項1~4のいずれか一項に記載のダイシングシート。 The dicing sheet according to any one of claims 1 to 4, wherein the substrate has a light transmittance of 40% or more at a wavelength of 1064 nm after the heating.  前記基材は、エチレンとプロピレンとの共重合体から構成されるフィルムであることを特徴とする請求項1~5のいずれか一項に記載のダイシングシート。 The dicing sheet according to any one of claims 1 to 5, wherein the base material is a film composed of a copolymer of ethylene and propylene.  前記ダイシングシートは、前記粘着剤層の前記基材側とは反対側の周縁部に積層された治具用粘着剤層を備えたことを特徴とする請求項1~6のいずれか一項に記載のダイシングシート。 The dicing sheet includes a jig pressure-sensitive adhesive layer laminated on a peripheral edge of the pressure-sensitive adhesive layer opposite to the base material side. The dicing sheet described.
PCT/JP2015/064181 2014-06-10 2015-05-18 Dicing sheet Ceased WO2015190230A1 (en)

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KR20180122317A (en) * 2016-03-04 2018-11-12 린텍 가부시키가이샤 Semiconductor processing sheet
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