US20060234159A1 - Photosensitive epoxy resin adhesive composition and use thereof - Google Patents

Photosensitive epoxy resin adhesive composition and use thereof Download PDF

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Publication number
US20060234159A1
US20060234159A1 US11/399,515 US39951506A US2006234159A1 US 20060234159 A1 US20060234159 A1 US 20060234159A1 US 39951506 A US39951506 A US 39951506A US 2006234159 A1 US2006234159 A1 US 2006234159A1
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Prior art keywords
epoxy resin
photosensitive
adhesive composition
epoxy equivalent
weight
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US11/399,515
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Miho Yamaguchi
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Nitto Denko Corp
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Nitto Denko Corp
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Assigned to NITTO DENKO CORPORATION reassignment NITTO DENKO CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: YAMAGUCHI, MIHO
Assigned to NITTO DENKO CORPORATION reassignment NITTO DENKO CORPORATION CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE'S ADDRESS PREVIOUSLY RECORDED ON REEL 017771, FRAME 0416. ASSIGNOR HEREBY CONFIRMS THE ASSIGNMENT OF THE ENTIRE INTEREST. Assignors: YAMAGUCHI, MIHO
Publication of US20060234159A1 publication Critical patent/US20060234159A1/en
Priority to US11/734,426 priority Critical patent/US7695586B2/en
Abandoned legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/68—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the catalysts used
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J163/00—Adhesives based on epoxy resins; Adhesives based on derivatives of epoxy resins
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2924/00—Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
    • H01L2924/0001—Technical content checked by a classifier
    • H01L2924/0002—Not covered by any one of groups H01L24/00, H01L24/00 and H01L2224/00

Definitions

  • the present invention relates to a photosensitive epoxy resin adhesive composition and its use; particularly to a photosensitive epoxy resin adhesive composition which is capable of forming a pattern by exposure to light through a photomask and development, and which, even after having formed a pattern in that manner, may still exhibit high adhesiveness with keeping its pattern as such by heating.
  • the present invention also relates to a photosensitive adhesive film which comprises the photosensitive epoxy resin adhesive composition.
  • the inner semiconductor packages for the appliances are being changed from lead frame-type packages to new-type high-density semiconductor packages such as BGA, CSP; and for example, for bonding a semiconductor chip to a circuit board or for bonding plural circuit boards together, use of a patterned adhesive is proposed (for example, see Reference 1).
  • a photosensitive adhesive composition heretofore known in the art is patterned by exposing it to light and developing it, whereupon the resin used in the composition is crosslinked and cured. Accordingly, when an object is adhered to the thus-patterned adhesive composition layer, then it must be applied to the layer under thermal pressure at a high temperature.
  • the conventional photosensitive adhesive composition is crosslinked and cured when it forms a pattern, and therefore even when an object is applied to the patterned layer under thermal pressure at such a high temperature, the adhesive composition could not be fully fluid even though it may be softened in some degree, and, as a result, there may occur partial voids in the adhesive interface between the adhesive and the object to be adhered.
  • An object of the present invention is to solve the above-mentioned problems with conventional photosensitive adhesive resin compositions and to provide a photosensitive epoxy resin adhesive composition which is capable of forming a pattern by exposure to light through a photomask and development, and which, even after having formed a pattern in that manner, may still exhibit high adhesiveness when heated while keeping its pattern as such, and to provide a photosensitive adhesive film that comprises the photosensitive epoxy resin adhesive composition.
  • the present invention provides a photosensitive epoxy resin adhesive composition comprising an epoxy resin and an photo-acid generator, wherein the epoxy resin comprises a polyfunctional epoxy resin having an epoxy equivalent of from 100 to 300 g/eq and a polyfunctional epoxy resin having an epoxy equivalent of from 450 to 10,000 g/eq.
  • the present invention also provides a photosensitive adhesive film that comprises the photosensitive epoxy resin adhesive composition.
  • the photosensitive epoxy resin adhesive composition of the present invention may form a pattern through exposure to light and development, and, in addition, even after having formed a pattern, it may still exhibit high adhesiveness by heating and excellent moisture-resistant reliability and excellent chemical resistance while keeping its pattern as such. Accordingly, the photosensitive epoxy resin adhesive composition of the present invention may form a micropattern on a first adherend with it, and then, while keeping the pattern, a second adherend may be applied to it under thermal compression whereby a desired space may be formed between the thus-bonded adherends.
  • the photosensitive epoxy resin adhesive composition of the present invention comprises an epoxy resin and an photo-acid generator, wherein the epoxy resin comprises a polyfunctional epoxy resin having an epoxy equivalent of from 100 to 300 g/eq, preferably from 150 to 280 g/eq (low-epoxy equivalent epoxy resin) and a polyfunctional epoxy resin having an epoxy equivalent of from 450 to 10,000 g/eq, preferably from 450 to 9,000 g/eq (high-epoxy equivalent epoxy resin).
  • the epoxy resin comprises a polyfunctional epoxy resin having an epoxy equivalent of from 100 to 300 g/eq, preferably from 150 to 280 g/eq (low-epoxy equivalent epoxy resin) and a polyfunctional epoxy resin having an epoxy equivalent of from 450 to 10,000 g/eq, preferably from 450 to 9,000 g/eq (high-epoxy equivalent epoxy resin).
  • the low-epoxy equivalent epoxy resin has a low melt viscosity and has good wettability in adhesion, and, in addition, it may form a high-resolution pattern through exposure to light and development.
  • the low-epoxy equivalent epoxy resin of this type is preferably a glycidyl ether-type epoxy resin, more preferably a bisphenol A-type, bisphenol F-type, biphenyl-type, novolak-type or fluorene-type glycidyl ether epoxy resin.
  • the high-epoxy equivalent epoxy resin has plasticity by itself, and therefore, the photosensitive epoxy resin adhesive composition of the present invention which contains it may be formed into a film.
  • the high-epoxy equivalent epoxy resin of this type is preferably a bisphenol A-type phenoxy resin or a bisphenol F-type phenoxy resin.
  • the phenoxy resin as referred to herein means an epoxy resin prepared by reaction of bisphenol A or bisphenol F with epichlorohydrin to thereby greatly increase its molecular weight.
  • the above-mentioned high-epoxy equivalent epoxy resin is combined with the above-mentioned low-epoxy equivalent epoxy resin to give a photosensitive epoxy resin adhesive composition which has excellent wettability to adherends, which may form a micropattern through exposure to light and development, which, even after having formed such a pattern, may still have high adhesiveness while keeping its pattern, and which may be formed into a film.
  • the epoxy resin preferably comprises from 5 to 90% by weight of the low-epoxy equivalent epoxy resin and from 10 to 95% by weight of the high-epoxy equivalent epoxy resin, more preferably from 10 to 60% by weight of the low-epoxy equivalent epoxy resin and from 40 to 90% by weight of the high-epoxy equivalent epoxy resin, furthermore preferably from 10 to 50% by weight of the low-epoxy equivalent epoxy resin and from 50 to 90% by weight of the high-epoxy equivalent epoxy resin (preferably 5:95 to 90:10 by weight, more preferably 10:90 to 60:40 by weight, furthermore preferably 10:90 to 50:50 by weight).
  • the resulting composition may not be formed into a film even when it is combined with the above-mentioned high-epoxy equivalent epoxy resin.
  • the proportion of the high-epoxy equivalent epoxy resin is too high, then the resulting composition may hardly form a micropattern through exposure to light and development even when it is combined with the above-mentioned low-epoxy equivalent epoxy resin and, in addition, the composition may not be able to form adhesion having good moisture-resistant reliability and good chemical resistance between the adherends.
  • a photo-acid generator is used along with the above-mentioned combination of epoxy resins to give a photosensitive epoxy resin adhesive composition.
  • the photo-acid generator generates an acid when the photosensitive epoxy resin adhesive composition is exposed to light, and the acid catalyses crosslinking and cure the epoxy resin in the composition, and therefore, the composition is photosensitive.
  • Any known photo-acid generators may be used herein, including, for example, various onium salts, especially triallylsulfonium salts and diallyliodonium salts with a counter anion such as BF 4 , PF 6 , AsF 6 or SbF 6 . These are commercially available.
  • the amount of the photo-acid generator to be in the composition may be generally from 1 to 15 parts by weight, preferably from 1 to 10 parts by weight relative to 100 parts by weight of the epoxy resin therein.
  • the photosensitive epoxy resin adhesive composition of the present invention may optionally contain, in addition to the above-mentioned low-epoxy equivalent epoxy resin, the high-epoxy equivalent epoxy resin and the photo-acid generator, any additives generally used in photosensitive adhesive compositions such as flame retardant, lubricant, leveling agent, etc.
  • the photosensitive epoxy resin adhesive composition of the present invention may be prepared and used as follows: The above-mentioned epoxy resin and the photo-acid generator and optional additive are dissolved in a suitable organic solvent such as dioxane or cyclohexane, and the resulting mixture is applied onto the surface of a first adherend, for example, a glass substrate, an organic substrate or a silicon substrate, for example, by the spin-coating method, and then dried to form a coating film thereon.
  • a suitable organic solvent such as dioxane or cyclohexane
  • a photomask this is exposed to suitable active rays such as UV rays, electron rays or microwaves, whereupon the epoxy resin is crosslinked and cured by the action of the photo-acid generator, as mentioned above, and then this is developed, i.e., the non-exposed area of the coating film is dissolved and removed by the use of a developer solvent, and thereafter, if desired, this is subjected to post-exposure heating, whereby an adhesive composition of a desired pattern may be formed on the first adherend.
  • a developer for example, herein usable is an organic solvent such as N-methyl-2-pyrrolidone or methyl ethyl ketone.
  • the dipping method or the spraying method may be employed.
  • Another embodiment of the present invention is as follows: The above-mentioned epoxy resin, the photo-acid generator and optional additive(s) are dissolved in a suitable organic solvent such as dioxane, and this is applied onto a suitable substrate and dried to form a film.
  • the resulting film may be transferred onto a first adherend, and, in the same manner as above, this is exposed to light via a photomask, whereupon the epoxy resin is crosslinked and cured by the action of the photo-acid generator, and then this is developed, and optionally further subjected to post-exposure heating, whereby an adhesive composition of a desired pattern may be formed on the adherend.
  • the thickness of the thus-patterned adhesive composition layer formed on the adherend is generally from 10 to 100 ⁇ m, preferably from 20 to 50 ⁇ m.
  • a second adherend is put on the adhesive composition layer thus formed on the first adherend to have a desired pattern, and heated under pressure generally at 90 to 200° C., preferably at 100 to 160° C. and generally under 1 to 200 kg/cm 2 , preferably 10 t 100 kg/cm 2 , whereby the first and second adherend may be bonded together with the patterned adhesive composition layer, while the pattern of the adhesive composition layer is kept as such.
  • the photosensitive epoxy resin adhesive composition of the present invention may be utilized as follows: A solution of the composition is applied onto a first adherend, or a film of the composition is transferred onto a first adherend, and then this is exposed to light and developed to form a suitable pattern on the first adherend so as to have a void space thereon, and thereafter a second adherend is put on it and subjected to thermal compression whereby an adhesion of high reliability is formed between the first and second adherends and, during this, a desired gap space may be formed between the two, corresponding to the above-mentioned void space.
  • the photosensitive adhesive film was transferred onto the surface of a glass plate at 80° C. Using a high-pressure mercury lamp, the photosensitive adhesive film on the surface of the glass plate was exposed to light via a photomask at 1000 mJ/cm 2 , and heated at 80° C. for 10 minutes after the exposure, and then developed with N-methyl-2-pyrrolidone as the developer, thereby forming a pattern of 100- ⁇ m wide lines aligned in parallel to each other at a pitch of 100 ⁇ m.
  • the photosensitive adhesive film was transferred onto a wafer, then its surface was completely exposed to light, heated at 80° C. for 10 minutes after the exposure, and thereafter developed with a developer of N-methyl-2-pyrrolidone. This was cut into small pieces of 3 mm ⁇ 3 mm in size, and thermally pressed against a slide glass plate at 150° C. under a pressure of 55 kg/cm 2 for 10 seconds. Then, this was further heated at 150° C. for 1 hour and was thus post-cured. The shear adhesive power measured was 5 MPa or more. These small pieces were tested for their moisture absorption by keeping them at a relative humidity of 90% for 200 hours, and after the test, the shear adhesive power thereof was still 5 MPa or more.
  • a photosensitive epoxy resin adhesive composition was prepared in the same manner as in Example 1, except that 40 parts by weight of biphenyl-type epoxy resin having an epoxy equivalent of 186 g/eq was used as a low-epoxy equivalent epoxy resin, and 60 parts by weight of bisphenol F-type phenoxy resin having an epoxy equivalent of 4400 g/eq was used as a high-epoxy equivalent epoxy resin. This was formed into a photosensitive adhesive film having a thickness of 35 ⁇ m.
  • the photosensitive adhesive film was patterned, and via the thus-patterned adhesive composition layer having a void space at a pitch of 30 ⁇ m, a pair of glass plates were bonded to each other. Also in the same manner as in Example 1, the photosensitive adhesive film was transferred onto a wafer, then its surface was completely exposed to light, heated after the exposure, developed, and then cut into small pieces of 3 mm ⁇ 3 mm in size, and thermally pressed against a slide glass plate. The shear adhesion power of the pieces measured was 5 MPa or more. After the moisture absorption test, the shear adhesion power of the small pieces was still 5 MPa or more.
  • a photosensitive epoxy resin adhesive composition was prepared in the same manner as in Example 1, except that 50 parts by weight of biphenyl-type epoxy resin having an epoxy equivalent of 186 g/eq was used as a low-epoxy equivalent epoxy resin, and 50 parts by weight of bisphenol F-type phenoxy resin having an epoxy equivalent of 4400 g/eq was used as a high-epoxy equivalent epoxy resin. This was formed into a photosensitive adhesive film having a thickness of 35 ⁇ m.
  • the photosensitive adhesive film was patterned on a glass plate, and via the thus-patterned adhesive composition layer having a void space at a pitch of 30 ⁇ m, a second glass plate was bonded to it. Also in the same manner as in Example 1, the photosensitive adhesive film was transferred onto a wafer, then its surface was completely exposed to light, heated after the exposure, developed, and then cut into small pieces of 3 mm ⁇ 3 mm in size, and thermally pressed against a slide glass plate. The shear adhesion power of the pieces measured was 5 MPa or more. After the moisture absorption test, the shear adhesion power of the small pieces was still 5 MPa or more.
  • a photosensitive epoxy resin adhesive composition was prepared in the same manner as in Example 1, except that 40 parts by weight of novolak-type epoxy resin having an epoxy equivalent of 177 g/eq was used as a low-epoxy equivalent epoxy resin, and 60 parts by weight of bisphenol F-type phenoxy resin having an epoxy equivalent of 8690 g/eq was used as a high-epoxy equivalent epoxy resin. This was formed into a photosensitive adhesive film having a thickness of 35 ⁇ m.
  • the photosensitive adhesive film was patterned on a glass plate, and via the thus-patterned adhesive composition layer having a void space at a pitch of 30 ⁇ m, a second glass plate was bonded to it. Also in the same manner as in Example 1, the photosensitive adhesive film was transferred onto a wafer, then its surface was completely exposed to light, heated after the exposure, developed, and then cut into small pieces of 3 mm ⁇ 3 mm in size, and thermally pressed against a slide glass plate. The shear adhesion power of the pieces measured was 5 MPa or more. After the moisture absorption test, the shear adhesion power of the small pieces was still 5 MPa or more.
  • a photosensitive epoxy resin adhesive composition was prepared in the same manner as in Example 1, except that 10 parts by weight of novolak-type epoxy resin having an epoxy equivalent of 177 g/eq was used as a low-epoxy equivalent epoxy resin, and 90 parts by weight of bisphenol A-type phenoxy resin having an epoxy equivalent of 475 g/eq was used as a high-epoxy equivalent epoxy resin. This was formed into a photosensitive adhesive film having a thickness of 35 ⁇ m.
  • the photosensitive adhesive film was patterned on a glass plate, and via the thus-patterned adhesive composition layer having a void space at a pitch of 30 ⁇ m, a second glass plate was bonded to it. Also in the same manner as in Example 1, the photosensitive adhesive film was transferred onto a wafer, then its surface was completely exposed to light, heated after the exposure, developed, and then cut into small pieces of 3 mm ⁇ 3 mm in size, and thermally pressed against a slide glass plate. The shear adhesion power of the pieces measured was 5 MPa or more. After the moisture absorption test, the shear adhesion power of the small pieces was still 5 MPa or more.
  • a photosensitive epoxy resin adhesive composition was prepared as a varnish thereof having a solid concentration of 50% by weight, except that a high-epoxy equivalent epoxy resin was not used, and 100 parts by weight of bisphenol A-type epoxy resin having an epoxy equivalent of 250 g/eq was used as a low-epoxy equivalent epoxy resin and 9 parts by weight of the same photo-acid generator as in Example 1 was used.
  • the varnish was applied onto a polyester film, heated at 80° C. and dried, but the coating film was extremely sticky. The varnish could not be formed into a dry photosensitive adhesive film.
  • a photosensitive epoxy resin adhesive composition was prepared as a varnish thereof having a solid concentration of 50% by weight, except that a low-epoxy equivalent epoxy resin was not used, and 100 parts by weight of bisphenol F-type epoxy resin having an epoxy equivalent of 8690 g/eq was used as a high-epoxy equivalent epoxy resin and 9 parts by weight of the same photo-acid generator as in Example 1 was used.
  • the varnish was applied onto a polyester film, heated at 80° C. and dried to obtain a photosensitive adhesive film having a thickness of 35 ⁇ m.
  • the photosensitive adhesive film was transferred onto the surface of a glass plate, exposed to light via a photomask, heated after the exposure, and developed, whereupon the film was swollen as a whole and could not form a pattern.
  • a photosensitive epoxy resin adhesive composition was prepared as a varnish thereof having a solid concentration of 50% by weight, except that a low-epoxy equivalent epoxy resin was not used, and 50 parts by weight of bisphenol A-type epoxy resin having an epoxy equivalent of 475 g/eq and 50 parts by weight of bisphenol F-type epoxy resin having an epoxy equivalent of 8690 g/eq were used as high-epoxy equivalent epoxy resins, and 9 parts by weight of the same photo-acid generator as in Example 1 was used.
  • the varnish was applied onto a polyester film, heated at 80° C. and dried to obtain a photosensitive adhesive film having a thickness of 35 ⁇ m.
  • the photosensitive adhesive film was patterned on a glass plate, and via the thus-patterned adhesive composition layer having a void space at a pitch of 30 ⁇ m, a second glass plate was bonded to it.
  • the photosensitive adhesive film was transferred onto a wafer, then its surface was completely exposed to light, heated after the exposure, developed, and then cut into small pieces of 3 mm ⁇ 3 mm in size, and thermally pressed against a slide glass plate.
  • the shear adhesion power of the pieces measured was 2 MPa. After the moisture absorption test, the shear adhesion power of the small pieces was less than 1 MPa.

Abstract

A photosensitive epoxy resin adhesive composition which is capable of forming a pattern by exposure to light through a photomask and development, and which, even after having formed a pattern in that manner, may still exhibit high adhesiveness when heated while keeping its pattern as such, as well as a photosensitive adhesive film which comprises the photosensitive epoxy resin adhesive composition. The photosensitive epoxy resin adhesive composition comprises an epoxy resin and a photo-acid generator, wherein the epoxy resin comprises a polyfunctional epoxy resin having an epoxy equivalent of from 100 to 300 g/eq and a polyfunctional epoxy resin having an epoxy equivalent of from 450 to 10000 g/eq.

Description

    FIELD OF THE INVENTION
  • The present invention relates to a photosensitive epoxy resin adhesive composition and its use; particularly to a photosensitive epoxy resin adhesive composition which is capable of forming a pattern by exposure to light through a photomask and development, and which, even after having formed a pattern in that manner, may still exhibit high adhesiveness with keeping its pattern as such by heating. The present invention also relates to a photosensitive adhesive film which comprises the photosensitive epoxy resin adhesive composition.
    • BACKGROUND OF THE INVENTION
  • With the recent tendency toward downsizing and increase in circuit integration of information communication appliances, the inner semiconductor packages for the appliances are being changed from lead frame-type packages to new-type high-density semiconductor packages such as BGA, CSP; and for example, for bonding a semiconductor chip to a circuit board or for bonding plural circuit boards together, use of a patterned adhesive is proposed (for example, see Reference 1).
  • In general, however, a photosensitive adhesive composition heretofore known in the art is patterned by exposing it to light and developing it, whereupon the resin used in the composition is crosslinked and cured. Accordingly, when an object is adhered to the thus-patterned adhesive composition layer, then it must be applied to the layer under thermal pressure at a high temperature. In addition, as so mentioned hereinabove, the conventional photosensitive adhesive composition is crosslinked and cured when it forms a pattern, and therefore even when an object is applied to the patterned layer under thermal pressure at such a high temperature, the adhesive composition could not be fully fluid even though it may be softened in some degree, and, as a result, there may occur partial voids in the adhesive interface between the adhesive and the object to be adhered. In general, therefore, it is difficult to obtain a sufficient adhesion strength between the adhesive and the object. Needless-to-say, semiconductor chips and circuit boards that are to be bonded with such an adhesive are damaged by heat, and primarily therefore, their adhesion at a high temperature must be preferably avoided, as mentioned above.
  • Reference 1: JP-A-2003-297876
    • SUMMARY OF THE INVENTION
  • An object of the present invention is to solve the above-mentioned problems with conventional photosensitive adhesive resin compositions and to provide a photosensitive epoxy resin adhesive composition which is capable of forming a pattern by exposure to light through a photomask and development, and which, even after having formed a pattern in that manner, may still exhibit high adhesiveness when heated while keeping its pattern as such, and to provide a photosensitive adhesive film that comprises the photosensitive epoxy resin adhesive composition.
  • The present invention provides a photosensitive epoxy resin adhesive composition comprising an epoxy resin and an photo-acid generator, wherein the epoxy resin comprises a polyfunctional epoxy resin having an epoxy equivalent of from 100 to 300 g/eq and a polyfunctional epoxy resin having an epoxy equivalent of from 450 to 10,000 g/eq. The present invention also provides a photosensitive adhesive film that comprises the photosensitive epoxy resin adhesive composition.
  • The photosensitive epoxy resin adhesive composition of the present invention may form a pattern through exposure to light and development, and, in addition, even after having formed a pattern, it may still exhibit high adhesiveness by heating and excellent moisture-resistant reliability and excellent chemical resistance while keeping its pattern as such. Accordingly, the photosensitive epoxy resin adhesive composition of the present invention may form a micropattern on a first adherend with it, and then, while keeping the pattern, a second adherend may be applied to it under thermal compression whereby a desired space may be formed between the thus-bonded adherends.
    • DETAILED DESCRIPTION OF THE INVENTION
  • The photosensitive epoxy resin adhesive composition of the present invention comprises an epoxy resin and an photo-acid generator, wherein the epoxy resin comprises a polyfunctional epoxy resin having an epoxy equivalent of from 100 to 300 g/eq, preferably from 150 to 280 g/eq (low-epoxy equivalent epoxy resin) and a polyfunctional epoxy resin having an epoxy equivalent of from 450 to 10,000 g/eq, preferably from 450 to 9,000 g/eq (high-epoxy equivalent epoxy resin).
  • In the photosensitive epoxy resin adhesive composition of the present invention, the low-epoxy equivalent epoxy resin has a low melt viscosity and has good wettability in adhesion, and, in addition, it may form a high-resolution pattern through exposure to light and development. The low-epoxy equivalent epoxy resin of this type is preferably a glycidyl ether-type epoxy resin, more preferably a bisphenol A-type, bisphenol F-type, biphenyl-type, novolak-type or fluorene-type glycidyl ether epoxy resin. On the other hand, the high-epoxy equivalent epoxy resin has plasticity by itself, and therefore, the photosensitive epoxy resin adhesive composition of the present invention which contains it may be formed into a film. For example, the high-epoxy equivalent epoxy resin of this type is preferably a bisphenol A-type phenoxy resin or a bisphenol F-type phenoxy resin. The phenoxy resin as referred to herein means an epoxy resin prepared by reaction of bisphenol A or bisphenol F with epichlorohydrin to thereby greatly increase its molecular weight.
  • In the present invention, the above-mentioned high-epoxy equivalent epoxy resin is combined with the above-mentioned low-epoxy equivalent epoxy resin to give a photosensitive epoxy resin adhesive composition which has excellent wettability to adherends, which may form a micropattern through exposure to light and development, which, even after having formed such a pattern, may still have high adhesiveness while keeping its pattern, and which may be formed into a film.
  • In the present invention, the epoxy resin preferably comprises from 5 to 90% by weight of the low-epoxy equivalent epoxy resin and from 10 to 95% by weight of the high-epoxy equivalent epoxy resin, more preferably from 10 to 60% by weight of the low-epoxy equivalent epoxy resin and from 40 to 90% by weight of the high-epoxy equivalent epoxy resin, furthermore preferably from 10 to 50% by weight of the low-epoxy equivalent epoxy resin and from 50 to 90% by weight of the high-epoxy equivalent epoxy resin (preferably 5:95 to 90:10 by weight, more preferably 10:90 to 60:40 by weight, furthermore preferably 10:90 to 50:50 by weight). If the proportion of the low-epoxy equivalent epoxy resin is too high, then the resulting composition may not be formed into a film even when it is combined with the above-mentioned high-epoxy equivalent epoxy resin. On the other hand, if the proportion of the high-epoxy equivalent epoxy resin is too high, then the resulting composition may hardly form a micropattern through exposure to light and development even when it is combined with the above-mentioned low-epoxy equivalent epoxy resin and, in addition, the composition may not be able to form adhesion having good moisture-resistant reliability and good chemical resistance between the adherends.
  • In the present invention, a photo-acid generator is used along with the above-mentioned combination of epoxy resins to give a photosensitive epoxy resin adhesive composition. Specifically, the photo-acid generator generates an acid when the photosensitive epoxy resin adhesive composition is exposed to light, and the acid catalyses crosslinking and cure the epoxy resin in the composition, and therefore, the composition is photosensitive. Any known photo-acid generators may be used herein, including, for example, various onium salts, especially triallylsulfonium salts and diallyliodonium salts with a counter anion such as BF4, PF6, AsF6 or SbF6. These are commercially available. In the present invention, the amount of the photo-acid generator to be in the composition may be generally from 1 to 15 parts by weight, preferably from 1 to 10 parts by weight relative to 100 parts by weight of the epoxy resin therein.
  • The photosensitive epoxy resin adhesive composition of the present invention may optionally contain, in addition to the above-mentioned low-epoxy equivalent epoxy resin, the high-epoxy equivalent epoxy resin and the photo-acid generator, any additives generally used in photosensitive adhesive compositions such as flame retardant, lubricant, leveling agent, etc.
  • The photosensitive epoxy resin adhesive composition of the present invention may be prepared and used as follows: The above-mentioned epoxy resin and the photo-acid generator and optional additive are dissolved in a suitable organic solvent such as dioxane or cyclohexane, and the resulting mixture is applied onto the surface of a first adherend, for example, a glass substrate, an organic substrate or a silicon substrate, for example, by the spin-coating method, and then dried to form a coating film thereon. Then, via a photomask, this is exposed to suitable active rays such as UV rays, electron rays or microwaves, whereupon the epoxy resin is crosslinked and cured by the action of the photo-acid generator, as mentioned above, and then this is developed, i.e., the non-exposed area of the coating film is dissolved and removed by the use of a developer solvent, and thereafter, if desired, this is subjected to post-exposure heating, whereby an adhesive composition of a desired pattern may be formed on the first adherend. For the developer, for example, herein usable is an organic solvent such as N-methyl-2-pyrrolidone or methyl ethyl ketone. For the development with such a developer, for example, the dipping method or the spraying method may be employed.
  • Another embodiment of the present invention is as follows: The above-mentioned epoxy resin, the photo-acid generator and optional additive(s) are dissolved in a suitable organic solvent such as dioxane, and this is applied onto a suitable substrate and dried to form a film. The resulting film may be transferred onto a first adherend, and, in the same manner as above, this is exposed to light via a photomask, whereupon the epoxy resin is crosslinked and cured by the action of the photo-acid generator, and then this is developed, and optionally further subjected to post-exposure heating, whereby an adhesive composition of a desired pattern may be formed on the adherend. The thickness of the thus-patterned adhesive composition layer formed on the adherend is generally from 10 to 100 μm, preferably from 20 to 50 μm.
  • Next, a second adherend is put on the adhesive composition layer thus formed on the first adherend to have a desired pattern, and heated under pressure generally at 90 to 200° C., preferably at 100 to 160° C. and generally under 1 to 200 kg/cm2, preferably 10 t 100 kg/cm2, whereby the first and second adherend may be bonded together with the patterned adhesive composition layer, while the pattern of the adhesive composition layer is kept as such.
  • Accordingly, the photosensitive epoxy resin adhesive composition of the present invention may be utilized as follows: A solution of the composition is applied onto a first adherend, or a film of the composition is transferred onto a first adherend, and then this is exposed to light and developed to form a suitable pattern on the first adherend so as to have a void space thereon, and thereafter a second adherend is put on it and subjected to thermal compression whereby an adhesion of high reliability is formed between the first and second adherends and, during this, a desired gap space may be formed between the two, corresponding to the above-mentioned void space.
  • The present invention is described concretely with reference to the following Examples, which, however, are not intended to restrict the scope of the present invention.
    • EXAMPLE 1
  • 10 parts by weight of bisphenol A-type epoxy resin having an epoxy equivalent of 250 g/eq, as a low-epoxy equivalent epoxy resin; 90 parts by weight of bisphenol F-type phenoxy resin having an epoxy equivalent of 8690 g/eq, as a high-epoxy equivalent epoxy resin; and 9 parts by weight of 4,4-bis[di(β-hydroxyethoxy)phenylsulfinio]phenylsulfide bis(hexafluoroantimonate) as a photo-acid generator were dissolved in dioxane to prepare a photosensitive epoxy resin adhesive composition as a varnish having a solid concentration of 50% by weight. The varnish was applied onto a polyester film, heated at 80° C. and dried to obtain a photosensitive adhesive film of the photosensitive epoxy resin adhesive composition having a thickness of 35 μm.
  • The photosensitive adhesive film was transferred onto the surface of a glass plate at 80° C. Using a high-pressure mercury lamp, the photosensitive adhesive film on the surface of the glass plate was exposed to light via a photomask at 1000 mJ/cm2, and heated at 80° C. for 10 minutes after the exposure, and then developed with N-methyl-2-pyrrolidone as the developer, thereby forming a pattern of 100-μm wide lines aligned in parallel to each other at a pitch of 100 μm. Next, using a laminator, another glass plate was stuck onto the pattern at a temperature of 150° C., and while the void space at a pitch of 30 μm resulting from the pattern of the photosensitive adhesive film was still kept as such between the glass plates, the pair of the glass plates were adhered to each other.
  • In the same manner, the photosensitive adhesive film was transferred onto a wafer, then its surface was completely exposed to light, heated at 80° C. for 10 minutes after the exposure, and thereafter developed with a developer of N-methyl-2-pyrrolidone. This was cut into small pieces of 3 mm×3 mm in size, and thermally pressed against a slide glass plate at 150° C. under a pressure of 55 kg/cm2 for 10 seconds. Then, this was further heated at 150° C. for 1 hour and was thus post-cured. The shear adhesive power measured was 5 MPa or more. These small pieces were tested for their moisture absorption by keeping them at a relative humidity of 90% for 200 hours, and after the test, the shear adhesive power thereof was still 5 MPa or more.
    • EXAMPLE 2
  • A photosensitive epoxy resin adhesive composition was prepared in the same manner as in Example 1, except that 40 parts by weight of biphenyl-type epoxy resin having an epoxy equivalent of 186 g/eq was used as a low-epoxy equivalent epoxy resin, and 60 parts by weight of bisphenol F-type phenoxy resin having an epoxy equivalent of 4400 g/eq was used as a high-epoxy equivalent epoxy resin. This was formed into a photosensitive adhesive film having a thickness of 35 μm.
  • Also in the same manner as in Example 1, the photosensitive adhesive film was patterned, and via the thus-patterned adhesive composition layer having a void space at a pitch of 30 μm, a pair of glass plates were bonded to each other. Also in the same manner as in Example 1, the photosensitive adhesive film was transferred onto a wafer, then its surface was completely exposed to light, heated after the exposure, developed, and then cut into small pieces of 3 mm×3 mm in size, and thermally pressed against a slide glass plate. The shear adhesion power of the pieces measured was 5 MPa or more. After the moisture absorption test, the shear adhesion power of the small pieces was still 5 MPa or more.
    • EXAMPLE 3
  • A photosensitive epoxy resin adhesive composition was prepared in the same manner as in Example 1, except that 50 parts by weight of biphenyl-type epoxy resin having an epoxy equivalent of 186 g/eq was used as a low-epoxy equivalent epoxy resin, and 50 parts by weight of bisphenol F-type phenoxy resin having an epoxy equivalent of 4400 g/eq was used as a high-epoxy equivalent epoxy resin. This was formed into a photosensitive adhesive film having a thickness of 35 μm.
  • Also in the same manner as in Example 1, the photosensitive adhesive film was patterned on a glass plate, and via the thus-patterned adhesive composition layer having a void space at a pitch of 30 μm, a second glass plate was bonded to it. Also in the same manner as in Example 1, the photosensitive adhesive film was transferred onto a wafer, then its surface was completely exposed to light, heated after the exposure, developed, and then cut into small pieces of 3 mm×3 mm in size, and thermally pressed against a slide glass plate. The shear adhesion power of the pieces measured was 5 MPa or more. After the moisture absorption test, the shear adhesion power of the small pieces was still 5 MPa or more.
    • EXAMPLE 4
  • A photosensitive epoxy resin adhesive composition was prepared in the same manner as in Example 1, except that 40 parts by weight of novolak-type epoxy resin having an epoxy equivalent of 177 g/eq was used as a low-epoxy equivalent epoxy resin, and 60 parts by weight of bisphenol F-type phenoxy resin having an epoxy equivalent of 8690 g/eq was used as a high-epoxy equivalent epoxy resin. This was formed into a photosensitive adhesive film having a thickness of 35 μm.
  • Also in the same manner as in Example 1, the photosensitive adhesive film was patterned on a glass plate, and via the thus-patterned adhesive composition layer having a void space at a pitch of 30 μm, a second glass plate was bonded to it. Also in the same manner as in Example 1, the photosensitive adhesive film was transferred onto a wafer, then its surface was completely exposed to light, heated after the exposure, developed, and then cut into small pieces of 3 mm×3 mm in size, and thermally pressed against a slide glass plate. The shear adhesion power of the pieces measured was 5 MPa or more. After the moisture absorption test, the shear adhesion power of the small pieces was still 5 MPa or more.
    • EXAMPLE 5
  • A photosensitive epoxy resin adhesive composition was prepared in the same manner as in Example 1, except that 10 parts by weight of novolak-type epoxy resin having an epoxy equivalent of 177 g/eq was used as a low-epoxy equivalent epoxy resin, and 90 parts by weight of bisphenol A-type phenoxy resin having an epoxy equivalent of 475 g/eq was used as a high-epoxy equivalent epoxy resin. This was formed into a photosensitive adhesive film having a thickness of 35 μm.
  • Also in the same manner as in Example 1, the photosensitive adhesive film was patterned on a glass plate, and via the thus-patterned adhesive composition layer having a void space at a pitch of 30 μm, a second glass plate was bonded to it. Also in the same manner as in Example 1, the photosensitive adhesive film was transferred onto a wafer, then its surface was completely exposed to light, heated after the exposure, developed, and then cut into small pieces of 3 mm×3 mm in size, and thermally pressed against a slide glass plate. The shear adhesion power of the pieces measured was 5 MPa or more. After the moisture absorption test, the shear adhesion power of the small pieces was still 5 MPa or more.
    • COMPARATIVE EXAMPLE 1
  • In the same manner as in Example 1, a photosensitive epoxy resin adhesive composition was prepared as a varnish thereof having a solid concentration of 50% by weight, except that a high-epoxy equivalent epoxy resin was not used, and 100 parts by weight of bisphenol A-type epoxy resin having an epoxy equivalent of 250 g/eq was used as a low-epoxy equivalent epoxy resin and 9 parts by weight of the same photo-acid generator as in Example 1 was used. The varnish was applied onto a polyester film, heated at 80° C. and dried, but the coating film was extremely sticky. The varnish could not be formed into a dry photosensitive adhesive film.
    • COMPARATIVE EXAMPLE 2
  • In the same manner as in Example 1, a photosensitive epoxy resin adhesive composition was prepared as a varnish thereof having a solid concentration of 50% by weight, except that a low-epoxy equivalent epoxy resin was not used, and 100 parts by weight of bisphenol F-type epoxy resin having an epoxy equivalent of 8690 g/eq was used as a high-epoxy equivalent epoxy resin and 9 parts by weight of the same photo-acid generator as in Example 1 was used. The varnish was applied onto a polyester film, heated at 80° C. and dried to obtain a photosensitive adhesive film having a thickness of 35 μm.
  • Also in the same manner as in Example 1, the photosensitive adhesive film was transferred onto the surface of a glass plate, exposed to light via a photomask, heated after the exposure, and developed, whereupon the film was swollen as a whole and could not form a pattern.
    • COMPARATIVE EXAMPLE 3
  • In the same manner as in Example 1, a photosensitive epoxy resin adhesive composition was prepared as a varnish thereof having a solid concentration of 50% by weight, except that a low-epoxy equivalent epoxy resin was not used, and 50 parts by weight of bisphenol A-type epoxy resin having an epoxy equivalent of 475 g/eq and 50 parts by weight of bisphenol F-type epoxy resin having an epoxy equivalent of 8690 g/eq were used as high-epoxy equivalent epoxy resins, and 9 parts by weight of the same photo-acid generator as in Example 1 was used. The varnish was applied onto a polyester film, heated at 80° C. and dried to obtain a photosensitive adhesive film having a thickness of 35 μm.
  • Also in the same manner as in Example 1, the photosensitive adhesive film was patterned on a glass plate, and via the thus-patterned adhesive composition layer having a void space at a pitch of 30 μm, a second glass plate was bonded to it. On the other hand and in the same manner as in Example 1, the photosensitive adhesive film was transferred onto a wafer, then its surface was completely exposed to light, heated after the exposure, developed, and then cut into small pieces of 3 mm×3 mm in size, and thermally pressed against a slide glass plate. The shear adhesion power of the pieces measured was 2 MPa. After the moisture absorption test, the shear adhesion power of the small pieces was less than 1 MPa.
  • While the invention has been described in detail and with reference to specific embodiments thereof, it will be apparent to one skilled in the art that various changes and modifications can be made therein without departing from the scope thereof.
  • This application is based on Japanese patent application No. 2005-121754 filed Apr. 19, 2005, the entire contents thereof being hereby incorporated by reference.

Claims (7)

1. A photosensitive epoxy resin adhesive composition comprising an epoxy resin and an photo-acid generator, wherein the epoxy resin comprises a first polyfunctional epoxy resin having an epoxy equivalent of from 100 to 300 g/eq and a second polyfunctional epoxy resin having an epoxy equivalent of from 450 to 10000 g/eq.
2. The photosensitive epoxy resin adhesive composition according to claim 1, wherein the first polyfunctional epoxy resin has an epoxy equivalent of from 150 to 280 g/eq.
3. The photosensitive epoxy resin adhesive composition according to claim 1, wherein the second polyfunctional epoxy resin has an epoxy equivalent of from 450 to 9,000 g/eq.
4. The photosensitive epoxy resin adhesive composition according to claim 1, wherein the ratio of the first polyfunctional epoxy resin and the second polyfunctional epoxy resin is 5:95 to 90:10 by weight.
5. The photosensitive epoxy resin adhesive composition according to claim 4, wherein the ratio of the first polyfunctional epoxy resin and the second polyfunctional epoxy resin is 10:90 to 60:40 by weight.
6. The photosensitive epoxy resin adhesive composition according to claim 5, wherein the ratio of the first polyfunctional epoxy resin and the second polyfunctional epoxy resin is 10:90 to 50:50 by weight.
7. A photosensitive adhesive film comprising the photosensitive epoxy resin adhesive composition of claim 1.
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100277037A1 (en) * 2006-12-28 2010-11-04 Kyocera Corporation Surface Acoustic Wave Device and Method of Manufacturing the Same
US20100314783A1 (en) * 2005-07-05 2010-12-16 Takashi Kawamori Photosensitive adhesive composition, and obtained using the same, adhesive film, adhesive sheet, semiconductor wafer with adhesive layer, semiconductor device and electronic part
US20110109704A1 (en) * 2009-11-11 2011-05-12 Seiko Epson Corporation Liquid droplet ejecting head, method for manufacturing the same, and liquid droplet ejecting apparatus

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5615512B2 (en) * 2009-04-27 2014-10-29 日東電工株式会社 Photosensitive resin composition, flexible circuit board using the same, and method for producing the circuit board
KR101377356B1 (en) 2012-12-26 2014-03-25 주식회사 두산 Epoxy resin composition having an excellent adhesive property and copper foil with resin
DE102013109755A1 (en) 2013-09-06 2015-03-12 Rent A Scientist Gmbh Conductive adhesive
KR101832522B1 (en) * 2013-11-29 2018-04-04 주식회사 엘지화학 Composition for forming adhesive film, adhesive film before light curing for further processing, adhesive film and electronic paper display

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4548890A (en) * 1983-03-31 1985-10-22 Sericol Group Limited Water-based photopolymerizable compositions and their use
US4957946A (en) * 1987-06-05 1990-09-18 Ciga-Geigy Corporation Cationically polymerizable mixtures containing metallocene complex salt of certain carboxylic or suffonic acids
US5144051A (en) * 1990-05-29 1992-09-01 Minnesota Mining And Manufacturing Company Branched alkoxyphenyl iodonium salt photoinitiators
US5252694A (en) * 1992-01-22 1993-10-12 Minnesota Mining And Manufacturing Company Energy-polymerization adhesive, coating, film and process for making the same
US5264325A (en) * 1988-12-30 1993-11-23 International Business Machines Corporation Composition for photo imaging
US5543266A (en) * 1985-06-26 1996-08-06 Canon Kabushiki Kaisha Active energy ray-curing resin composition
US5766277A (en) * 1996-09-20 1998-06-16 Minnesota Mining And Manufacturing Company Coated abrasive article and method of making same

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62277421A (en) * 1986-05-26 1987-12-02 Matsushita Electric Works Ltd One-pack type sealant for sealing semiconductor
EP0430881A3 (en) 1989-11-29 1991-10-23 Ciba-Geigy Ag Photochromic compounds, process for their preparation and their use
AU672337B2 (en) * 1993-10-27 1996-09-26 Nippon Paint Co., Ltd. Curable resin composition for coating uses
DE69738783D1 (en) * 1996-10-08 2008-07-31 Hitachi Chemical Co Ltd SEMICONDUCTOR ARRANGEMENT, SEMICONDUCTOR CHIP SUPPLEMENT, ARRANGEMENT METHOD FOR ARRANGEMENT AND SUBSTRATE, ADHESIVE AND DOUBLE-SIDED ADHESIVE TAPE
JP2002069159A (en) * 2000-08-30 2002-03-08 Hitachi Ltd Photosensitive epoxy resin composition
JP3893303B2 (en) 2002-03-29 2007-03-14 住友ベークライト株式会社 Manufacturing method of semiconductor package
JP2003313274A (en) * 2002-04-25 2003-11-06 Dainippon Ink & Chem Inc Ultraviolet-curable composition and optical disk using the same

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4548890A (en) * 1983-03-31 1985-10-22 Sericol Group Limited Water-based photopolymerizable compositions and their use
US5543266A (en) * 1985-06-26 1996-08-06 Canon Kabushiki Kaisha Active energy ray-curing resin composition
US4957946A (en) * 1987-06-05 1990-09-18 Ciga-Geigy Corporation Cationically polymerizable mixtures containing metallocene complex salt of certain carboxylic or suffonic acids
US5264325A (en) * 1988-12-30 1993-11-23 International Business Machines Corporation Composition for photo imaging
US5144051A (en) * 1990-05-29 1992-09-01 Minnesota Mining And Manufacturing Company Branched alkoxyphenyl iodonium salt photoinitiators
US5252694A (en) * 1992-01-22 1993-10-12 Minnesota Mining And Manufacturing Company Energy-polymerization adhesive, coating, film and process for making the same
US5766277A (en) * 1996-09-20 1998-06-16 Minnesota Mining And Manufacturing Company Coated abrasive article and method of making same

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8323873B2 (en) 2005-07-05 2012-12-04 Hitachi Chemical Company, Ltd. Photosensitive adhesive composition, and obtained using the same, adhesive film, adhesive sheet, semiconductor wafer with adhesive layer, semiconductor device and electronic part
US20100314783A1 (en) * 2005-07-05 2010-12-16 Takashi Kawamori Photosensitive adhesive composition, and obtained using the same, adhesive film, adhesive sheet, semiconductor wafer with adhesive layer, semiconductor device and electronic part
US20110065260A1 (en) * 2005-07-05 2011-03-17 Takashi Kawamori Photosensitive adhesive composition, and obtained using the same, adhesive film, adhesive sheet, semiconductor wafer with adhesive layer, semiconductor device and electronic part
US20110065043A1 (en) * 2005-07-05 2011-03-17 Takashi Kawamori Photosensitive adhesive composition, and obtained using the same, adhesive film, adhesive sheet, semiconductor wafer with adhesive layer, semiconductor device and electronic part
US20110079927A1 (en) * 2005-07-05 2011-04-07 Takashi Kawamori Photosensitive adhesive composition, and obtained using the same, adhesive film, adhesive sheet, semiconductor wafer with adhesive layer, semiconductor device and electronic part
US8293453B2 (en) * 2005-07-05 2012-10-23 Hitachi Chemical Company, Ltd. Photosensitive adhesive composition, and obtained using the same, adhesive film, adhesive sheet, semiconductor wafer with adhesive layer, semiconductor device and electronic part
US8445177B2 (en) 2005-07-05 2013-05-21 Hitachi Chemical Company, Ltd. Photosensitive adhesive composition, and obtained using the same, adhesive film, adhesive sheet, semiconductor wafer with adhesive layer, semiconductor device and electronic part
US8673539B2 (en) 2005-07-05 2014-03-18 Hitachi Chemical Company, Ltd. Photosensitive adhesive composition, and obtained using the same, adhesive film, adhesive sheet, semiconductor wafer with adhesive layer, semiconductor device and electronic part
US8008837B2 (en) 2006-12-28 2011-08-30 Kyocera Corporation Surface acoustic wave device and method of manufacturing the same
CN101573868B (en) * 2006-12-28 2012-05-30 京瓷株式会社 Surface acoustic wave device and method for manufacturing the same
US20100277037A1 (en) * 2006-12-28 2010-11-04 Kyocera Corporation Surface Acoustic Wave Device and Method of Manufacturing the Same
US20110109704A1 (en) * 2009-11-11 2011-05-12 Seiko Epson Corporation Liquid droplet ejecting head, method for manufacturing the same, and liquid droplet ejecting apparatus
US8820897B2 (en) 2009-11-11 2014-09-02 Seiko Epson Corporation Liquid droplet ejecting head, method for manufacturing the same, and liquid droplet ejecting apparatus

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