WO2011043471A1 - Composition d'agent de démoulage, film anti-adhésif, et film adhésif sensible à la pression - Google Patents
Composition d'agent de démoulage, film anti-adhésif, et film adhésif sensible à la pression Download PDFInfo
- Publication number
- WO2011043471A1 WO2011043471A1 PCT/JP2010/067784 JP2010067784W WO2011043471A1 WO 2011043471 A1 WO2011043471 A1 WO 2011043471A1 JP 2010067784 W JP2010067784 W JP 2010067784W WO 2011043471 A1 WO2011043471 A1 WO 2011043471A1
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- Prior art keywords
- film
- release
- polyester resin
- agent composition
- silicone
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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
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C33/00—Moulds or cores; Details thereof or accessories therefor
- B29C33/56—Coatings, e.g. enameled or galvanised; Releasing, lubricating or separating agents
- B29C33/68—Release sheets
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/80—Masked polyisocyanates
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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
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/40—Adhesives in the form of films or foils characterised by release liners
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2067/00—Use of polyesters or derivatives thereof, as moulding material
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2083/00—Use of polymers having silicon, with or without sulfur, nitrogen, oxygen, or carbon only, in the main chain, as moulding material
Definitions
- the present invention relates to a release agent composition, a release film and an adhesive film, and more particularly to a release film useful as a protective film for an anisotropic conductive film and a release agent composition for forming the release layer.
- a release film with a release agent coating (release layer) on one side of a release base material such as a polyester film is an adhesive for electronic devices such as an anisotropic conductive film (ACF). It is widely used as a protective film for various adhesive coatings including adhesive coatings. That is, the pressure-sensitive adhesive film for electronic devices is usually formed by applying a coating liquid containing a pressure-sensitive adhesive and a solvent on the surface of the base film and then heating to remove the solvent. The release film is laminated on the surface of this pressure-sensitive adhesive film and used as a protective film.
- a silicone release agent is generally used to reduce the surface energy, and in particular, an addition reaction type silicone release agent that cures at a relatively low temperature in a short time.
- a mold is used (Patent Documents 1 and 2).
- the addition reaction type silicone release agent is cured (crosslinking reaction) with a metal catalyst such as platinum, and is prepared to have a desired release function (for example, the surface tension ( ⁇ S) of the silicone release layer is 19). ⁇ About 21 dyne / cm).
- the release layer of the release film has a certain degree of affinity for the adhesive film.
- the present invention was created in order to solve the above-described disadvantages of the prior art, and an object thereof is to provide a release film and an adhesive film in which the jerky phenomenon does not appear, and such a release film and an adhesive film.
- An object of the present invention is to provide a release agent composition for forming a release layer.
- thermoplastic saturated polyester resin other than silicone added to the coating liquid of the release agent composition, and form a mixture of silicone and thermoplastic saturated polyester resin.
- a sea-island structure non-uniform structure is obtained in which a large number of regions of thermoplastic saturated polyester resin are dispersed unevenly in the sea where silicone is a continuous phase, resulting in a jerky phenomenon where the peel force is not stable It was found that can be improved.
- the present invention was created based on the above discovery, and is a release agent composition containing an addition reaction type silicone, a curing catalyst for curing the addition reaction type silicone, and a thermoplastic saturated polyester resin. is there.
- the release agent composition of the present invention when the release agent composition is formed into a film, a sea-island structure in which the polyester resin regions are dispersed non-uniformly in a continuous phase of silicone is formed. Is.
- the release agent composition of the present invention preferably contains a blocked isocyanate crosslinking agent that crosslinks the polyester resin.
- the blocked isocyanate crosslinking agent is a crosslinking agent in which an isocyanate group is blocked with a protecting group, and the protecting group is dissociated when heated to a temperature higher than the curing temperature of the addition reaction type silicone.
- the solid component of the polyester resin is preferably 5 parts by weight or more and 100 parts by weight or less, more preferably 7 parts by weight or more, with respect to 100 parts by weight of the solid component of the silicone. It is preferably contained in an amount of 50 parts by weight or less, particularly preferably in the range of 10 parts by weight to 30 parts by weight.
- the present invention also provides a release film in which a release layer formed of the above release agent composition is laminated on a film substrate, and the release film and the release layer of the release film An adhesive film having an adhesive layer laminated thereon is provided.
- a release film in which a release layer formed of the above release agent composition is laminated on a film substrate, and the release film and the release layer of the release film An adhesive film having an adhesive layer laminated thereon is provided.
- the pressure-sensitive adhesive film an aspect in which the pressure-sensitive adhesive layer contains conductive particles and is used as an anisotropic conductive film is provided.
- the release agent composition of the present invention contains a silicone resin which is an addition reaction type resin and a thermoplastic saturated polyester resin.
- silicone is used in the release layer formed by forming a film of this release agent composition.
- a sea-island structure is formed in which the thermoplastic saturated polyester resin is dispersed non-uniformly in an irregular shape in the sea with the resin as a continuous phase.
- the polyester resin which is an island of sea-island structure, improves the affinity between the release layer and the adhesive layer in contact with the release layer. Therefore, in the adhesive film in which the release layer and the adhesive layer are laminated, The jerky phenomenon is remarkably suppressed and the peeling force is stabilized.
- the polyester resin contained in the release layer is transferred from the release layer to the adhesive layer, dropped off, or the adhesive layer is peeled off to the release layer. There is no inconvenience such as, and a decrease in the residual adhesion rate can be prevented in the pressure-sensitive adhesive layer after the release layer is peeled from the pressure-sensitive adhesive film.
- the polyester resin can be cross-linked during film formation of the release agent composition.
- the residual adhesive force is not reduced in the pressure-sensitive adhesive layer after peeling the release layer, and the solvent-resistant residual adhesive rate of the release layer is improved.
- a release film using the release agent composition of the present invention for the release layer is suitable as a protective film for the anisotropic conductive film, and an adhesive film in which the anisotropic conductive film is laminated on the release film of the present invention. Is useful as an anisotropic conductive film.
- the pressure-sensitive adhesive film of the present invention is useful as a pressure-sensitive adhesive film (adhesive tape) having no jerky phenomenon for electric component arrangement regardless of the presence or absence of conductive particles in the pressure-sensitive adhesive layer.
- the mold release agent composition of the present invention contains an addition reaction type silicone, a curing catalyst for curing the addition reaction type silicone, and a thermoplastic saturated polyester resin.
- the release layer can be cured at a low temperature in a short time as compared with the condensation type silicone.
- the addition reaction type silicone for example, a known polydimethylsiloxane having an alkenyl group (for example, vinyl group, hexenyl group, etc.) in the molecule can be used.
- Specific examples of the addition reaction type silicone include materials such as trade names X52-9201B, KS847, and KS830 manufactured by Shin-Etsu Chemical Co., Ltd.
- a known platinum-based curing catalyst can be preferably exemplified.
- platinum-based curing catalysts include chloroplatinic acid, complex salts of chloroplatinic acid and olefins, and compounds of chloroplatinic acid and alcohols.
- the amount is preferably 0.5 to 5 parts by weight, more preferably 0.5 to 2 parts by weight (including the solvent) with respect to 100 parts by weight (including the solvent) of the solution.
- thermoplastic saturated polyester resin has a number average molecular weight of 1,000 to 50,000, more preferably 5,000 to 30,000, a softening point of 50 ° C. to 250 ° C., more preferably 130 ° C. to 200 ° C., and a glass transition point of 40 ° C. to 90 ° C.
- Specific examples of preferred thermoplastic saturated polyester resins include Elitel UE-3200 (number average molecular weight 16000, softening point 165 ° C., glass transition point 65 ° C.), Elitel UE-3201 (number average molecular weight 20000, softening point 165) manufactured by Unitika Ltd.
- the content of the thermoplastic saturated polyester resin in the release agent composition of the present invention is preferably 5 to 100 parts by weight, more preferably 7 parts by weight of the solid component of the thermoplastic saturated polyester resin with respect to 100 parts by weight of the solid component of silicone. -50 parts by weight, more preferably 10-30 parts by weight.
- the polyester content is excessively small, the sea-island structure cannot be effectively formed in the release layer formed from the release agent composition, and the affinity between the release layer and the adhesive layer cannot be improved.
- the polyester content is excessively large, the coating film performance is adversely affected, and repellency, unevenness, and streaks are likely to occur, and the release performance is also adversely affected.
- the thermoplastic saturated polyester resin may be crosslinked or not crosslinked.
- the polyester is contained in the silicone cured product.
- the release force can be adjusted by dispersing the lump of resin in the form of islands, but the thermoplastic saturated polyester resin is preferably crosslinked, and the release agent composition of the present invention is thermoplastic saturated. It is preferable to contain a crosslinking agent for crosslinking the polyester resin.
- thermoplastic saturation polyester resin itself does not proceed with the crosslinking reaction. Therefore, if a solvent that is soluble in polyester resin or a solvent that is highly compatible with polyester resin is used as the solvent for the adhesive layer to be laminated with the release layer, it is included in the release layer when the release layer and the adhesive layer are peeled off.
- the polyester resin that has been transferred causes transfer or dropping to the pressure-sensitive adhesive layer, resulting in an increase in peeling force and a decrease in peelability, or a decrease in the residual adhesion rate in the pressure-sensitive adhesive layer after peeling.
- the isocyanate-based crosslinking agent that crosslinks the polyester resin to the release agent composition.
- the isocyanate-based crosslinking agent is a catalyst poison of the platinum-based curing catalyst for curing the silicone.
- a system crosslinking agent cannot be blended.
- the cross-linking agent in which the NCO group of the polyisocyanate is blocked with a protecting group is called a blocked isocyanate cross-linking agent.
- a blocked isocyanate cross-linking agent When heated above the temperature at which the protecting group dissociates, the NCO group and the polyester resin from which the protecting group is dissociated It is possible to crosslink between the polyester resins by reacting with the hydroxy group.
- the temperature at which the addition reaction type silicone is cured does not become a catalyst poison of the curing catalyst and is heated to a temperature higher than the curing temperature of the addition reaction type silicone. Then, a blocked isocyanate cross-linking agent from which the protecting group is dissociated is contained.
- the crosslinking agent is activated when the temperature of the release agent composition is increased after completion of the curing reaction of the addition reaction type silicone, and the polyester resin is crosslinked. be able to. Therefore, when the pressure-sensitive adhesive layer laminated on the release layer is peeled from the release layer, the polyester resin can be prevented from being transferred from the release layer to the pressure-sensitive adhesive layer.
- block isocyanate-based crosslinking agent examples include trade name Coronate 2513 (dissociation condition: 120 ° C. ⁇ 30 minutes), Coronate 2507 (dissociation condition: 130 ° C. ⁇ 30 minutes) of Nippon Polyurethane Industry Co., Ltd.
- the weight ratio of solid content of a thermoplastic saturated polyester resin and a block isocyanate type crosslinking agent has preferable 5: 5 to 9: 1. If the amount of blocked isocyanate is more than 5: 5, it remains in the coating film and affects the release performance. If the amount of polyester resin is more than 9: 1, the reaction is not completed, which is not preferable.
- the release agent composition of the present invention can contain a solvent such as toluene, methyl ethyl ketone (MEK), xylene, acetone, hexane, ethyl acetate, MIBK, a release control agent, and the like for improving the coating property. . Moreover, it can prepare by mixing the component mentioned above uniformly by a conventional method.
- a solvent such as toluene, methyl ethyl ketone (MEK), xylene, acetone, hexane, ethyl acetate, MIBK, a release control agent, and the like for improving the coating property. .
- MEK methyl ethyl ketone
- MIBK methyl ethyl ketone
- the release film of the present invention is obtained by laminating a release layer on a film substrate, and the release layer is formed by film formation of the release agent composition of the present invention.
- the film substrate a known film substrate such as a polyester film can be used.
- the film substrate can be subjected to a surface treatment such as a corona treatment in order to improve the adhesion with the release layer.
- a surface treatment such as a corona treatment
- the film forming of the release composition can be performed as follows. That is, the release agent composition of the present invention is applied to a film substrate with a coil bar or the like to form a coating film of the release agent composition, and this is heated to cure the addition-reactive silicone, and the release agent When the composition contains a blocked isocyanate crosslinking agent, the release layer is formed by further raising the temperature until the dissociation temperature of the blocked isocyanate crosslinking agent is exceeded and crosslinking the polyester resin.
- the release agent composition it is preferable to dry and heat-harden rapidly after coating the release agent composition in order to form a sea-island structure. Therefore, for example, after applying the release agent composition to the film substrate at room temperature (10 to 35 ° C.), it is preferably in a constant temperature heating chamber of 130 to 180 ° C., more preferably 150 to 170 ° C., preferably 10 to 300 ° C. Heat for 2 seconds, more preferably 40 to 120 seconds. When the heating temperature is lower than 130 ° C., the silicone is not sufficiently cured, and when it exceeds 180 ° C., it is not preferable from the viewpoint of the heat resistance and heat shrinkability of the substrate.
- a release film in which a release layer having a sea-island structure is disposed on a film substrate can be obtained.
- the pressure-sensitive adhesive film of the present invention is obtained by laminating a pressure-sensitive adhesive layer on the release layer of the above-described release film.
- the pressure-sensitive adhesive layer is not limited to one that exhibits adhesiveness at room temperature.
- the main component of the adhesive layer may be formed of a thermoplastic resin, or may exhibit adhesiveness by heating.
- the adhesive layer can be formed on the anisotropic conductive film by containing conductive particles. Therefore, the pressure-sensitive adhesive film of the present invention containing conductive particles in the pressure-sensitive adhesive layer is useful as an anisotropic conductive adhesive film.
- Example 1 10 parts by weight of a 20% solution of polyester (trade name UE3200, manufactured by Unitika Ltd., number average molecular weight 16000, glass transition point 65 ° C.), 30% addition reaction type silicone solution (trade name KS-3703, manufactured by Shin-Etsu Chemical Co., Ltd.) 15 Parts by weight, 30% addition reaction type release control agent (trade name KS-3800, manufactured by Shin-Etsu Chemical Co., Ltd.), 0.3 parts by weight of a platinum curing catalyst (trade name PL-50T, manufactured by Shin-Etsu Chemical Co., Ltd.), A release agent composition was prepared by uniformly mixing 1 part by weight of a block isocyanate-based crosslinking agent (trade name Coronate 2513, manufactured by Nippon Polyurethane Industry Co., Ltd.), 30 parts by weight of toluene and 33 parts by weight of MEK.
- a block isocyanate-based crosslinking agent trade name Coronate 2513, manufactured by Nippon Polyurethane Industry Co.,
- the obtained release agent composition was applied to one side of a 50 ⁇ m-thick polyethylene terephthalate film as a film base with a coil bar so that the dry thickness was 0.3 ⁇ m, and placed in an oven at 160 ° C., and the temperature was set to 1. After holding for a minute, it was taken out from the oven, thereby obtaining a release film in which a release layer was provided on one side of the film substrate.
- Example 2 A release agent composition was prepared in the same manner as in Example 1 except that 1 part by weight of a blocked isocyanate-based crosslinking agent (trade name Coronate 2513, manufactured by Nippon Polyurethane Industry Co., Ltd.) was not added to obtain a release film.
- a blocked isocyanate-based crosslinking agent trade name Coronate 2513, manufactured by Nippon Polyurethane Industry Co., Ltd.
- Example 1 A method similar to Example 1 except that 20 parts by weight of 10% ethylcellulose solution (trade name N100, manufactured by Hercules USA) was added instead of 10 parts by weight of 20% solution of polyester (trade name UE3200, manufactured by Unitika Ltd.). The release agent composition was adjusted to obtain a release film.
- 10% ethylcellulose solution trade name N100, manufactured by Hercules USA
- polyester trade name UE3200, manufactured by Unitika Ltd.
- Liquid reactive epoxy (trade name PF-55TA, manufactured by PI i Japan Co., Ltd.), which is a constituent material of the anisotropic conductive film, is applied on the release layer of the release film. And then dried in an 80 ° C. oven for 5 minutes to drive off the solvent, and then further dried by aging in an 80 ° C. oven for 5 hours to form an epoxy resin film on the release film, and then the epoxy resin film was peeled off. .
- Adhesive film (Sony Chemical & Information Device Co., Ltd., trade name: T4090) with acrylic resin as the main component was bonded to the release surface of the release film, and the residual peel strength was measured in the same manner as described above to determine the residual adhesion rate (standard The ratio to the peel force (%)) was calculated, and the obtained value was defined as the solvent-resistant residual adhesion rate.
- Table 1 Adhesive film (Sony Chemical & Information Device Co., Ltd., trade name: T4090) with acrylic resin as the main component was bonded to the release surface of the release film, and the residual peel strength was measured in the same manner as described above to determine the residual adhesion rate (standard The ratio to the peel force (%)) was calculated, and the obtained value was defined as the solvent-resistant residual adhesion rate.
- Table 1 The obtained results are shown in Table 1.
- a residual adhesive rate and a solvent-resistant residual adhesive rate the value of 80% or more is calculated
- An adhesive film (PP tape manufactured by Nitto Denko Corporation) with an acrylic adhesive layer provided on a polypropylene base material is bonded to the anisotropic conductive film of this adhesive film, and is a strip shape having a length of 200 mm and a width of 50 mm.
- a T-type peel test is performed to peel the anisotropic conductive film from the release film at 25 ° C., and the initial peel force (g / 5 cm) is measured using a peel strength tester (trade name Tensilon manufactured by Orientec Co., Ltd.) And measured. The obtained results are shown in Table 1.
- Example 1 in Table 1 by using a blocked isocyanate-based crosslinking agent as a crosslinking agent for the polyester resin, initial peeling force, initial residual adhesion rate, solvent resistance residual adhesion rate, anisotropic conductive film peeling Both force and jerky properties are improved, and it can be seen that it is suitable as a release film for an anisotropic conductive film.
- the blocked isocyanate crosslinking agent since the blocked isocyanate crosslinking agent is not used, the polyester resin does not undergo a crosslinking reaction.
- the anisotropic conductive film peeling force and the solvent-resistant residual adhesion Although the rate is small, the jerky property is good, and it can be seen that it is sufficiently suitable as a release film for a general adhesive.
- Comparative Example 1 In the case of Comparative Example 1, by using a cellulosic resin instead of the polyester resin, the initial residual adhesive rate and the solvent resistance residual adhesive rate are greatly inferior compared to Example 1 using the polyester resin. It is inferior to Example 2 which does not carry out the polyester crosslinking reaction. In the case of Comparative Example 2, since no polyester resin was used, the affinity with the adhesive was poor and a jerky phenomenon occurred.
- Example 3 In order to investigate the influence on the jerky properties due to the type of polyester, a release agent composition in which only the type of polyester was changed in the same amount as in Example 1 was prepared, and the obtained release agent composition was prepared in the same manner as in Example 1. A plurality of release films were obtained by processing, and the above-mentioned (d) anisotropic conductive film peeling force (adhesive strength) test was conducted.
- polyester resin used The name of the polyester resin used and the value of the measured adhesive strength are shown in FIG.
- Each product name is a polyester resin manufactured by Unitika. Polyester having a small variation in measured peel force means that no jerky phenomenon occurred. From the measurement result of FIG. 2, the polyester to be added is preferably UE3200 or UE9200. More preferred is UE3200.
- Example 4 The addition amount of the polyester resin has little influence on the jerky phenomenon. However, when the addition amount is increased, the film performance of the release layer after applying the ACF, that is, the solvent resistance is lowered.
- the same type of polyester (UE3200) as in Example 1 was used, and the amount of components other than polyester was the same as in Example 1.
- the amount of polyester added was 0 to 200% of solid component relative to 100 parts by weight of the solid component of silicone.
- the release agent composition was adjusted within the range described above, and the obtained release agent composition was treated in the same manner as in Example 1 to prepare a plurality of types of release films.
- the obtained release film was measured for the aforementioned (d) anisotropic conductive film peeling force (adhesion strength) and (c) solvent resistance residual adhesion rate (residual adhesion rate).
- the measurement results are shown in the graph of FIG. From the graph of FIG. 3, it can be seen that the amount of polyester added has little effect on the jerky phenomenon, but as the amount added increases, the solvent resistance of the release layer after applying the anisotropic conductive film decreases. .
- the polyester is preferably added in an amount of 5 to 100 parts by weight (ie, 5 to 100% in FIG. 3), more preferably 10 to 30 parts by weight (ie, 100 parts by weight of the solid component of silicone). 10 to 30% in FIG. Moreover, when the addition amount of polyester exceeds 150% of FIG. 3 with respect to a silicone resin, it turns out that a residual adhesive rate falls and it is not preferable.
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- Medicinal Chemistry (AREA)
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Abstract
Cette invention concerne une composition d'agent de démoulage qui ne provoque
pas de phénomène de démoulage saccadé et un film anti-adhésif formé à partir de ladite composition.
La composition d'agent de démoulage selon l'invention comprend une silicone obtenue par une réaction d'addition, un catalyseur de durcissage pour durcir la silicone obtenue par la réaction d'addition, et une résine polyester saturé thermoplastique. Cette composition donne un film contenant des particules de résine polyester dispersées dans la silicone durcie.
Priority Applications (1)
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KR1020127009006A KR101732753B1 (ko) | 2009-10-08 | 2010-10-08 | 이형제 조성물, 이형 필름 및 점착 필름 |
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JP2009234011 | 2009-10-08 | ||
JP2009-234011 | 2009-10-08 |
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WO2011043471A1 true WO2011043471A1 (fr) | 2011-04-14 |
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PCT/JP2010/067784 WO2011043471A1 (fr) | 2009-10-08 | 2010-10-08 | Composition d'agent de démoulage, film anti-adhésif, et film adhésif sensible à la pression |
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JP (1) | JP5742161B2 (fr) |
KR (1) | KR101732753B1 (fr) |
TW (1) | TWI502028B (fr) |
WO (1) | WO2011043471A1 (fr) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
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US20150361235A1 (en) * | 2013-02-06 | 2015-12-17 | Mitsubishi Plastics, Inc. | Release film |
JP2019147909A (ja) * | 2018-02-28 | 2019-09-05 | 旭化成ワッカーシリコーン株式会社 | ブロックポリイソシアネート組成物を含有する硬化性シリコーン組成物またはシリコーン組成物キット、基材と一体成形物を得る製造方法および得られた一体成形物 |
JP2020070357A (ja) * | 2018-10-31 | 2020-05-07 | 旭化成ワッカーシリコーン株式会社 | 熱解離性ブロックポリイソシアネート組成物を含有する難燃性、または、自消性の硬化性シリコーン組成物。 |
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JP5956483B2 (ja) * | 2014-02-28 | 2016-07-27 | 三菱樹脂株式会社 | 積層ポリエステルフィルム |
WO2015141551A1 (fr) * | 2014-03-19 | 2015-09-24 | リンテック株式会社 | Composition d'agent antiadhésif, film antiadhésif, rouleau de film antiadhésif et procédé de production dudit rouleau |
JP5948000B2 (ja) * | 2014-07-28 | 2016-07-06 | 三菱樹脂株式会社 | 積層ポリエステルフィルム |
JP6406145B2 (ja) * | 2015-07-18 | 2018-10-17 | 三菱ケミカル株式会社 | 積層ポリエステルフィルム |
KR102518776B1 (ko) * | 2017-12-27 | 2023-04-10 | 도요보 가부시키가이샤 | 세라믹 그린 시트 제조용 이형 필름 |
US20220017758A1 (en) * | 2018-11-23 | 2022-01-20 | Basf Coatings Gmbh | Self-releasing in-mold coating (imc) for coating substrates |
JP2022183682A (ja) * | 2021-05-31 | 2022-12-13 | 日東電工株式会社 | 積層フィルム |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4947155B1 (fr) * | 1968-05-09 | 1974-12-13 | ||
JPS61136572A (ja) * | 1984-12-06 | 1986-06-24 | Nitto Electric Ind Co Ltd | 剥離性処理層 |
JP2003020347A (ja) * | 2001-07-10 | 2003-01-24 | Mitsubishi Polyester Film Copp | シリコーン含有ポリエステルフィルム |
JP2004091754A (ja) * | 2002-09-04 | 2004-03-25 | Sony Chem Corp | 離型剤組成物、離型フィルム及びその製造方法 |
JP2009088465A (ja) * | 2007-09-14 | 2009-04-23 | Hitachi Chem Co Ltd | 異方導電性接着剤、異方導電性フィルムおよび回路接続構造体の製造方法 |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001115111A (ja) * | 1999-08-11 | 2001-04-24 | Oji Paper Co Ltd | 剥離性シートおよび粘着テープ |
-
2010
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- 2010-10-08 JP JP2010228798A patent/JP5742161B2/ja active Active
- 2010-10-08 TW TW099134555A patent/TWI502028B/zh active
- 2010-10-08 WO PCT/JP2010/067784 patent/WO2011043471A1/fr active Application Filing
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4947155B1 (fr) * | 1968-05-09 | 1974-12-13 | ||
JPS61136572A (ja) * | 1984-12-06 | 1986-06-24 | Nitto Electric Ind Co Ltd | 剥離性処理層 |
JP2003020347A (ja) * | 2001-07-10 | 2003-01-24 | Mitsubishi Polyester Film Copp | シリコーン含有ポリエステルフィルム |
JP2004091754A (ja) * | 2002-09-04 | 2004-03-25 | Sony Chem Corp | 離型剤組成物、離型フィルム及びその製造方法 |
JP2009088465A (ja) * | 2007-09-14 | 2009-04-23 | Hitachi Chem Co Ltd | 異方導電性接着剤、異方導電性フィルムおよび回路接続構造体の製造方法 |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20150361235A1 (en) * | 2013-02-06 | 2015-12-17 | Mitsubishi Plastics, Inc. | Release film |
JP2019147909A (ja) * | 2018-02-28 | 2019-09-05 | 旭化成ワッカーシリコーン株式会社 | ブロックポリイソシアネート組成物を含有する硬化性シリコーン組成物またはシリコーン組成物キット、基材と一体成形物を得る製造方法および得られた一体成形物 |
WO2019166243A1 (fr) * | 2018-02-28 | 2019-09-06 | Wacker Chemie Ag | Composition de silicone durcissable ou kit de composition de silicone comprenant une composition de polyisocyanate bloquée, procédé de production pour obtenir un produit moulé d'un seul tenant avec un matériau de base, et produit moulé d'un seul tenant |
JP2020070357A (ja) * | 2018-10-31 | 2020-05-07 | 旭化成ワッカーシリコーン株式会社 | 熱解離性ブロックポリイソシアネート組成物を含有する難燃性、または、自消性の硬化性シリコーン組成物。 |
Also Published As
Publication number | Publication date |
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TW201122059A (en) | 2011-07-01 |
KR101732753B1 (ko) | 2017-05-04 |
TWI502028B (zh) | 2015-10-01 |
JP2011099097A (ja) | 2011-05-19 |
JP5742161B2 (ja) | 2015-07-01 |
KR20120082420A (ko) | 2012-07-23 |
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