JPWO2008018252A1 - 接着性組成物及びそれを用いた部材の仮固定方法 - Google Patents
接着性組成物及びそれを用いた部材の仮固定方法 Download PDFInfo
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- JPWO2008018252A1 JPWO2008018252A1 JP2008528752A JP2008528752A JPWO2008018252A1 JP WO2008018252 A1 JPWO2008018252 A1 JP WO2008018252A1 JP 2008528752 A JP2008528752 A JP 2008528752A JP 2008528752 A JP2008528752 A JP 2008528752A JP WO2008018252 A1 JPWO2008018252 A1 JP WO2008018252A1
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- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 229920006311 Urethane elastomer Polymers 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 150000008062 acetophenones Chemical class 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 229920000800 acrylic rubber Polymers 0.000 description 1
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 1
- 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
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- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 230000001588 bifunctional effect Effects 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- 229930006711 bornane-2,3-dione Natural products 0.000 description 1
- 150000001634 bornane-2,3-dione derivatives Chemical class 0.000 description 1
- 235000019437 butane-1,3-diol Nutrition 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
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- 238000001816 cooling Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
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- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- TZAMQIAPGYOUKF-UHFFFAOYSA-N diethoxyphosphoryl(phenyl)methanone Chemical compound CCOP(=O)(OCC)C(=O)C1=CC=CC=C1 TZAMQIAPGYOUKF-UHFFFAOYSA-N 0.000 description 1
- XVKKIGYVKWTOKG-UHFFFAOYSA-N diphenylphosphoryl(phenyl)methanone Chemical compound C=1C=CC=CC=1P(=O)(C=1C=CC=CC=1)C(=O)C1=CC=CC=C1 XVKKIGYVKWTOKG-UHFFFAOYSA-N 0.000 description 1
- VFHVQBAGLAREND-UHFFFAOYSA-N diphenylphosphoryl-(2,4,6-trimethylphenyl)methanone Chemical compound CC1=CC(C)=CC(C)=C1C(=O)P(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 VFHVQBAGLAREND-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 238000010556 emulsion polymerization method Methods 0.000 description 1
- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 description 1
- 229940009714 erythritol Drugs 0.000 description 1
- 235000019414 erythritol Nutrition 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 229940119545 isobornyl methacrylate Drugs 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- REEZZSHJLXOIHL-UHFFFAOYSA-N octanoyl chloride Chemical compound CCCCCCCC(Cl)=O REEZZSHJLXOIHL-UHFFFAOYSA-N 0.000 description 1
- 239000011242 organic-inorganic particle Substances 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 229950000688 phenothiazine Drugs 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- OXNIZHLAWKMVMX-UHFFFAOYSA-N picric acid Chemical compound OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O OXNIZHLAWKMVMX-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920001610 polycaprolactone Polymers 0.000 description 1
- 239000004632 polycaprolactone Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 230000008313 sensitization Effects 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J4/00—Adhesives based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; adhesives, based on monomers of macromolecular compounds of groups C09J183/00 - C09J183/16
-
- 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
- C09J133/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
- C09J133/04—Homopolymers or copolymers of esters
- C09J133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
- C09J11/08—Macromolecular additives
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J133/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
- C09J133/04—Homopolymers or copolymers of esters
- C09J133/14—Homopolymers or copolymers of esters of esters containing halogen, nitrogen, sulfur or oxygen atoms in addition to the carboxy oxygen
-
- 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
- C09J5/00—Adhesive processes in general; Adhesive processes not provided for elsewhere, e.g. relating to primers
- C09J5/06—Adhesive processes in general; Adhesive processes not provided for elsewhere, e.g. relating to primers involving heating of the applied adhesive
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K7/00—Use of ingredients characterised by shape
- C08K7/16—Solid spheres
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
- C08L2666/04—Macromolecular compounds according to groups C08L7/00 - C08L49/00, or C08L55/00 - C08L57/00; Derivatives thereof
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
- C08L33/10—Homopolymers or copolymers of methacrylic acid esters
- C08L33/12—Homopolymers or copolymers of methyl methacrylate
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L35/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical, and containing at least one other carboxyl radical in the molecule, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L35/06—Copolymers with vinyl aromatic monomers
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2301/00—Additional features of adhesives in the form of films or foils
- C09J2301/50—Additional features of adhesives in the form of films or foils characterized by process specific features
- C09J2301/502—Additional features of adhesives in the form of films or foils characterized by process specific features process for debonding adherents
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/25—Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
- Y10T428/254—Polymeric or resinous material
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Macromonomer-Based Addition Polymer (AREA)
Abstract
Description
本発明の目的は、このような特性を兼ね備えた接着性組成物、及びそれを用いた部材の仮固定方法を提供することにある。
(1)(A)多官能(メタ)アクリレート、(B)単官能(メタ)アクリレート、及び(C)光重合開始剤を含有する接着性組成物であって、該接着性組成物から得られる硬化体のガラス転移温度が−50℃〜40℃であることを特徴する接着性組成物。
(A)多官能(メタ)アクリレートとして、日本合成化学社製「UV-3000B」(ポリエステル系ウレタンアクリレート、以下「UV−3000B」と略す)30質量部、ジシクロぺンタニルジアクリレート(日本化薬社製「KAYARAD R−684」、以下「R−684」と略す)15質量部;(B)単官能(メタ)アクリレートとして、2−(1,2−シクロヘキサカルボキシイミド)エチルアクリレート(東亜合成化学社製「アロニックスM−140」、以下「M−140」と略す)20質量部、フェノールエチレンオキサイド2モル変成アクリレート(東亜合成化学社製「アロニックスM−101A」、以下「M−101A」と略す)35質量部;(C)光重合開始剤として、I−907:2−メチル−1−[4−(メチルチオ)フェニル]−2−モルフォリノプロパン−1−オン(チバ・スペシャルティ・ケミカルズ社製「IRGACURE907」、以下「IRGACURE907」又は単に「I−907」と略す)1質量部;粒状物質(D)として、平均粒径100μm、粒径(μm)を対数で表示したときの粒径に対する粒子体積分布の標準偏差0.063、比重1.05の球状架橋ポリスチレン粒子(ガンツ化成社製「GS−100S」)を1質量部;重合禁止剤として、MDP(2,2−メチレン−ビス(4−メチル−tブチルフェノール、住友化学社製スミライザーMDP−S)0.1質量部、を添加して樹脂組成物(接着性組成物)を作製した。得られた樹脂組成物を使用して、以下に示す評価方法にてガラス転移温度、引張せん断接着強さ、液比重の測定及び剥離試験を行った。それらの結果を表1に示す。また、粒状物質(D)の平均粒径、及び粒径(μm)を対数で表示したときの粒径に対する粒子体積分布の標準偏差も測定した。
表1、表2に示す種類の原材料を表1、表2に示す組成で使用したこと以外は実施例1と同様にして樹脂組成物を作製した。得られた組成物について、実施例1と同様にガラス転移温度、引張せん断接着強さ、液比重の測定及び剥離試験を行った。また、粒状物質(D)の平均粒径及び粒径(μm)を対数で表示したときの粒径に対する粒子体積分布の標準偏差も測定した。それらの結果を表1、表2に示す。
粒状物質(D)として平均粒子径60μm、粒径(μm)を対数で表示したときの粒径に対する粒子体積分布の標準偏差0.086、比重1.05の球状架橋ポリスチレン粒子(綜研化学社製「SGP−150C」)を使用し、表3、表4に示す種類の原材料を表3、表4に示す組成で使用したこと以外は実施例1と同様にして樹脂組成物を作製した。得られた組成物について、実施例1と同様の測定を行った。それらの結果を表3、表4に示す。
粒状物質(D)として平均粒子径58μm、粒径(μm)を対数で表示したときの粒径に対する粒子体積分布の標準偏差0.078、比重1.05の球状架橋ポリスチレン粒子(綜研化学社製「SGP−150C」を目開き63μmの篩と53μmの篩を用いて篩分けして作製)を使用し、表3に示す種類の原材料を表3に示す組成で使用したこと以外は実施例1と同様にして樹脂組成物を作製した。得られた組成物について、実施例1と同様の測定を行った。それらの結果を表3に示す。
粒状物質(D)として平均粒子径140μm、粒径(μm)を対数で表示したときの粒径に対する粒子体積分布の標準偏差0.074、比重1.14の球状架橋ポリメチルメタクリレート粒子(ガンツ化成社製「GM−5003」を目開き150μmの篩と125μmの篩を用いて篩分けして作製)を使用し、表3に示す種類の原材料を表3に示す組成で使用したこと以外は実施例1と同様にして樹脂組成物を作製した。得られた組成物について、実施例1と同様の測定を行った。それらの結果を表3に示す。
粒状物質(D)として平均粒子径70μm、粒径(μm)を対数で表示したときの粒径に対する粒子体積分布の標準偏差0.073、比重1.14の球状架橋ポリメチルメタクリレート粒子(ガンツ化成社製「GM−5003」を目開き75μmの篩と63μmの篩を用いて篩分けして作製)を使用し、表3に示す種類の原材料を表3に示す組成で使用したこと以外は実施例1と同様にして樹脂組成物を作製した。得られた組成物について、実施例1と同様の測定を行った。それらの結果を表3に示す。
粒状物質(D)として平均粒子径40μm、粒径(μm)を対数で表示したときの粒径に対する粒子体積分布の標準偏差0.071、比重1.14の球状架橋ポリメチルメタクリレート粒子(ガンツ化成社製「GM−5003」を目開き45μmの篩と38μmの篩を用いて篩分けして作製)を使用し、表3に示す種類の原材料を表3に示す組成で使用したこと以外は実施例1と同様にして樹脂組成物を作製した。得られた組成物について、実施例1と同様の測定を行った。それらの結果を表3に示す。
粒状物質(D)を使用しないこと以外は実施例1と同様にして樹脂組成物を作製した。得られた樹脂組成物について、実施例1と同様の測定を行った。それらの結果を表5に示す。
BDK:ベンジルジメチルケタール(チバ・スペシャルティ・ケミカルズ社製「IRGACURE651」)
UV−3700B:ポリエーテル系ウレタンアクリレート(日本合成化学社製「UV−3700B」)
UV−7000B:ポリエステル系ウレタンアクリレート(日本合成化学社製「UV−7000B」)
1.6−HX−A:1,6−ヘキサンジオールジアクリレート(共栄社化学社製「ライトアクリレート1.6−HX−A」)
EC−A:エトキシジエチレングリコールジアクリレート(共栄社化学社製「ライトアクリレートEC−A」)
QM:ジシクロペンテニルオキシエチルメタクリレート(ローム&ハース社製「QM−657」)
BZ:ベンジルメタクリレート(共栄社化学社製「ライトエステルBZ」)
IBX:イソボルニルメタクリレート(共栄社化学社製「ライトエステルIB−X」)
2−HEMA:2-ヒドロキシエチルメタクリレート
N−ビニルピロリドン:N−ビニルピロリドン(日本触媒社製)
実施例2及び5の樹脂組成物を使用し、実施例1と同様に剥離試験体を作製し、温水の温度を40℃、50℃、60、70℃に変えて剥離試験を行った。その結果を表6に示す。その結果、いずれの温度でも剥離性を有する。
実施例2の樹脂組成物を用いて、縦150mm×横150mm×厚さ2mmの板状耐熱パイレックスガラスと、実施例1で用いた青板ガラス(ダミーガラスとして使用)とを、実施例1と同様に接着硬化させた。この接着試験体の耐熱パイレックスガラス部分のみをダイシング装置を使用して10mm角に切断した。切断中に耐熱パイレックスガラスの脱落は発生せず、良好な加工性を示した。耐熱パイレックスガラス部分のみを切断した接着試験体を80℃の温水に浸漬したところ、60分ですべて剥離した。また、その剥離した切断試験片を無作為に10個取り出し、その切断試験片の裏面(樹脂組成物で仮固定した面)の各片を光学顕微鏡を用いて観察し、ガラスが欠けている箇所の最大幅を測定し、その平均値と標準偏差を求めた。その結果を、表7に示す。
ホットメルト型接着剤(日化精工社製「アドフィックスA」)を90℃に加熱し溶解させて、150mm×150mm×2mmの耐熱パイレックスガラスと、実施例1で用いた青板ガラスとを接着させた。この接着試験体の耐熱パイレックスガラス部分のみをダイシング装置を使用して10mm角に切断した。切断中に耐熱パイレックスガラスの脱落は発生せず、良好な加工性を示した。その試験片をN-メチルピドリロン溶液に1日浸漬し、切断試験片を回収し、実施例26と同様に剥離した切断試験片を任意に10個取り出し、その切断試験片の裏面(ホットメルト型接着剤で仮固定した面)の各片を光学顕微鏡を用いて観察し、ガラスが欠けている箇所の最大幅を測定し、その平均値と標準偏差を求めた。その結果を、表6に示す。
UV硬化型PET粘着テープを使用して150mm×150mm×2mmの耐熱パイレックスガラスを接着させた。この接着試験体の耐熱パイレックスガラス部分のみをダイシング装置を使用して10mm角に切断した。その試験片の粘着テープ部分に紫外線を照射させることにより粘着力を低下させ、その切断試験片を回収した。その切断試験片を実施例26と同様に剥離した切断試験片を任意に10個取り出し、その切断試験片の裏面(粘着テープで仮固定した面)の各片を光学顕微鏡を用いて観察し、ガラスが欠けている箇所の最大幅を測定し、その平均値と標準偏差を求めた。その結果を、表6に示す。
表6より、本発明の仮固定方法は、部品加工時のチッピング発生の防止の点で特に優れることが示される。
Claims (11)
- (A)多官能(メタ)アクリレート、(B)単官能(メタ)アクリレート、及び(C)光重合開始剤を含有する接着性組成物であって、該接着性組成物から得られる硬化体のガラス転移温度が−50℃〜40℃であることを特徴する接着性組成物。
- (A)及び(B)がいずれも疎水性である請求項1に記載の接着性組成物。
- (A)及び(B)を、(A):(B)=5:95〜95:5(質量部)の割合で含有し、(A)及び(B)の合計100質量部に対して、(C)を0.1〜20質量部含有する請求項1又は2に記載の接着性組成物。
- (A)、(B)、(C)のいずれにも溶解しない粒状物質(D)を、(A)及び(B)の合計100質量部に対して、0.1〜20質量部含有する請求項1〜3のいずれか1項に記載の接着性組成物。
- (D)の比重が、該接着性組成物の比重と等しいか、若しくは小さい請求項4に記載の接着性組成物。
- (D)の形状が球状である請求項4又は5に記載の接着性組成物。
- (D)が、架橋ポリメタクリル酸メチル粒子、架橋ポリスチレン粒子、及び架橋ポリメタクリル酸メチルポリスチレン共重合体粒子のいずれか、若しくはそれらの一部又は全部の混合物である請求項4〜6のいずれか1項に記載の接着性組成物。
- レーザー法による(D)の平均粒径が20〜200μmである請求項4〜7のいずれか1項に記載の接着性組成物。
- レーザー法による(D)の粒径(μm)を対数で表示したときの粒径に対する粒子体積分布の標準偏差が0.0001〜0.25の範囲にある請求項4〜8のいずれか1項に記載の接着性組成物。
- 請求項1〜9のいずれか1項に記載の接着性組成物を用いて部材を接着し固定してなる構造体。
- 請求項1〜9のいずれか1項に記載の接着性組成物を用いて部材を接着して仮固定し、該仮固定された部材を加工後、該加工された部材を90℃以下の温水に浸漬して、前記接着性組成物の硬化体を部材から取り外すことを特徴とする部材の仮固定方法。
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EP2050799A4 (en) | 2012-06-13 |
US7988811B2 (en) | 2011-08-02 |
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EP2050799B1 (en) | 2014-06-18 |
CN101501152B (zh) | 2013-11-13 |
SG174041A1 (en) | 2011-09-29 |
CN101501152A (zh) | 2009-08-05 |
TWI460245B (zh) | 2014-11-11 |
JP5247447B2 (ja) | 2013-07-24 |
KR20090025231A (ko) | 2009-03-10 |
KR101073153B1 (ko) | 2011-10-12 |
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