WO2016114010A1 - エマルション型粘着剤組成物 - Google Patents
エマルション型粘着剤組成物 Download PDFInfo
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- WO2016114010A1 WO2016114010A1 PCT/JP2015/082958 JP2015082958W WO2016114010A1 WO 2016114010 A1 WO2016114010 A1 WO 2016114010A1 JP 2015082958 W JP2015082958 W JP 2015082958W WO 2016114010 A1 WO2016114010 A1 WO 2016114010A1
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—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 a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
- C08F220/1808—C8-(meth)acrylate, e.g. isooctyl (meth)acrylate or 2-ethylhexyl (meth)acrylate
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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
- 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
Definitions
- the present invention relates to an emulsion-type pressure-sensitive adhesive composition comprising a mixture of at least two types of emulsions, and more specifically, it has excellent emulsion liquid stability and forms a pressure-sensitive adhesive layer despite its low viscosity.
- the present invention relates to a technique for providing an emulsion-type pressure-sensitive adhesive composition in which the pressure-sensitive adhesive layer exhibits high adhesive strength and high tack.
- ⁇ Adhesives are used in many fields such as tapes, sheets, labels, stickers and wallpaper.
- the material of the adherend covers a wide range, such as plastic, metal, glass, ceramics, paper, cloth, wood or fresh food.
- natural rubber, synthetic rubber, acrylic copolymer, or the like has been used as the main component of the pressure-sensitive adhesive, and these materials can be dissolved in an organic solvent or in water.
- a dispersed emulsion type is known.
- solvent-type pressure-sensitive adhesives harmful gases are generated when burned due to a fire, etc., and there are environmental hygiene problems due to organic solvents that volatilize when manufacturing pressure-sensitive adhesive layers.
- water-based emulsion types have begun to increase.
- emulsion-type pressure-sensitive adhesives mainly composed of an acrylic copolymer having excellent adhesiveness and weather resistance have been widely used.
- the composition of acrylic copolymers can be adjusted, and chain transfer agents and crosslinking agents can be used.
- high adhesive strength is achieved.
- each method has a limit in achieving a pressure-sensitive adhesive that achieves high adhesive strength and high tack.
- achieving high adhesive force is also performed by adding tackifying resin (tackifier).
- tackifying resin tackifier
- high adhesive strength has been achieved by adjusting the softening point and addition amount of the tackifying resin.
- this method has its limitations.
- Patent Document 1 proposes an acrylic emulsion for the purpose of improving adhesiveness to materials such as urethane foam whose surface is not smooth. Specifically, two types of acrylic monomer dispersions having different tackifiers dissolved therein are prepared, and after the polymerization reaction of one acrylic monomer dispersion is performed, the other acrylic monomer dispersion is added. The polymerization reaction is further performed to obtain an acrylic emulsion.
- Patent Documents 2 and 3 propose an emulsion-type pressure-sensitive adhesive composition with improved performances for polyolefin resins.
- an oil-soluble component composed of an ethylenically unsaturated monomer (A) and a tackifier (B) is added to specific particles using an emulsifier (C) in an aqueous medium.
- the resin emulsion [II] obtained by polymerizing the emulsion [I] emulsified to a diameter in the presence of the polymerization initiator (D) the (meth) acrylic acid alkyl ester is further added.
- An emulsion-type pressure-sensitive adhesive composition obtained by polymerizing an ethylenically unsaturated monomer (E) as a component is disclosed.
- Patent Document 3 a specific monomer, a tackifier resin, and an anionic surfactant are emulsified and dispersed to obtain a monomer emulsion having a specific particle size.
- This is a water-soluble polymerization initiator and an anionic surfactant.
- a method for producing a synthetic resin aqueous emulsion of polymer particles having a specific particle size by polymerizing while dropping into an aqueous solution for polymerization is disclosed.
- Patent Document 4 proposes an emulsion-type pressure-sensitive adhesive composition containing a low Tg polymer emulsion, a high Tg polymer emulsion, a crosslinking agent, and a tackifier resin. And according to this technology, even if the amount of tackifying resin used is reduced, it has high adhesion to both difficult-to-adhere adherends such as polyolefin and rough adherends such as corrugated cardboard. It shows strength and is also excellent in the balance between cohesion and tack.
- Patent Document 6 proposes an aqueous pressure-sensitive adhesive composition comprising an acrylic pressure-sensitive adhesive emulsion (A) and a copolymer emulsion (B) having a specific particle diameter and glass transition temperature. And it shows the adhesiveness which was excellent with respect to the film of nonpolar polymers like polyolefin, and it is said that the contact bonding layer is excellent in secondary processability, such as cutting. And it is described that the acrylic adhesive emulsion (A) which is a main component contains a functional group-containing (meth) acrylic acid alkyl ester copolymer and a tackifying resin.
- the purpose of the present invention is to establish a technology that can effectively use the tackifying resin without causing a new problem to the adhesive by adding the tackifying resin, It is to provide an emulsion-type pressure-sensitive adhesive composition excellent in environmental adaptability, in which the formed pressure-sensitive adhesive layer can achieve high adhesive strength and high tack, and can be applied at high speed because of low viscosity. .
- the present invention provides a low-Tg acrylic adhesive emulsion (A) as a main component in a range of 51 to 90% by mass and a high-Tg copolymer emulsion (B) as a secondary component in a range of 10 to 49% by mass.
- An emulsion-type pressure-sensitive adhesive composition comprising a mixture of at least these two types of emulsions, wherein the solid content is 50% or more, the viscosity at 25 ° C. is 1000 mPa ⁇ s or less, and the low Tg
- the acrylic pressure-sensitive adhesive emulsion (A) has a glass transition temperature (Tg) of ⁇ 70 ° C.
- the high-Tg copolymer emulsion (B) is at least a (meth) acrylic acid alkyl ester.
- Tg glass transition temperature
- An emulsion-type pressure-sensitive adhesive composition is provided.
- the amount of the tackifying resin is in the range of 40 to 120 parts by mass with respect to 100 parts by mass of the monomer mixture containing the (meth) acrylic acid alkyl ester monomer, and the copolymer
- the weight average molecular weight of 5,000 to 60,000; 60 to 80% by mass of the low-Tg acrylic adhesive emulsion (A), and 20 to 40% by mass of the high-Tg copolymer emulsion (B) as an auxiliary component.
- the viscosity of the low Tg acrylic pressure-sensitive adhesive emulsion (A) at 25 ° C.
- the tackifying resin is in the range of 50 to 700 mPa ⁇ s
- the high Tg copolymer emulsion (B ) In the range of 50 to 1000 mPa ⁇ s
- the softening point (° C.) of the tackifying resin is in the range of 70 to 170 ° C.
- an adhesive layer having a high adhesive force and a high tack is formed by a low-viscosity adhesive that has been demanded in recent years because the coating amount can be reduced or coating can be performed at high speed.
- An emulsion-type pressure-sensitive adhesive composition with excellent performance that can be provided is provided.
- the emulsion-type pressure-sensitive adhesive composition of the present invention comprises a low-Tg acrylic pressure-sensitive adhesive emulsion (A) as a main component to which a tackifying resin is added and a high-Tg co-weight as a subcomponent.
- the combined emulsion (B) exhibits the above-described excellent performance while having a simple structure containing a mixture of at least two types of emulsions.
- an emulsion having an excellent property can be obtained by an extremely simple structure in which a tackifier resin is present at the stage of obtaining a copolymer emulsion (B) as a subcomponent by emulsion polymerization without using a special process.
- the mold pressure-sensitive adhesive composition can be realized.
- in the aqueous coating composition obtained by mixing the emulsion-type pressure-sensitive adhesive composition of the present invention in addition to being able to reduce the manufacturing cost, it is particularly low even though the tackifying resin is contained in a high concentration. Even if it is a thing of a viscosity, since it becomes the thing of the outstanding property which does not produce the problem of isolation
- FIG 3 is a graph showing the particle size distribution of the copolymer emulsion (B-1) obtained in Synthesis Example 2 constituting the emulsion type pressure-sensitive adhesive composition of the present invention.
- (meth) acryl in the claims and the specification of the present invention means both “acryl” and “methacryl”, and the term “(meth) acrylate” "And” methacrylate ".
- the present inventors have obtained a mixture of polymer emulsions having different glass transition temperatures (Tg), no matter how the mixing ratio is changed.
- Tg glass transition temperatures
- the present inventors have realized that the desired performance desired by the present invention cannot be realized. That is, when polymer emulsions having different glass transition temperatures (Tg) are mixed and used as a base, the low Tg portion has a high tack but a low holding force (adhesive strength), while the high Tg portion has a holding force.
- the tack is low but the tack is low, it is sufficient to use a pressure-sensitive adhesive having a high holding power and a high tack.
- these two types can be used regardless of how the mixing ratio is changed.
- a combination of only polymer emulsions having different Tg's could not realize an adhesive having high holding power and high tack.
- the present inventors as a high-Tg copolymer emulsion (B), which is a secondary component, contain a (meth) acrylic acid alkyl ester monomer in the presence of a specific amount of tackifier resin.
- a high-Tg copolymer emulsion (B) which is a secondary component, contain a (meth) acrylic acid alkyl ester monomer in the presence of a specific amount of tackifier resin.
- the high-Tg copolymer emulsion (B) constituted as described above has improved tack, high holding power and high tack, and further uses this as a subcomponent, thereby providing a tackifying resin. Therefore, the emulsion-type pressure-sensitive adhesive composition of the present invention, which is mixed with the low-Tg acrylic pressure-sensitive adhesive emulsion (A) as the main component, has a low coating amount.
- the formed pressure-sensitive adhesive layer can achieve a high adhesive force and a high tack, and furthermore, since it has a low viscosity, excellent properties capable of high-speed coating are realized.
- the present inventors consider the reason why the emulsion-type pressure-sensitive adhesive composition of the present invention has the above-described excellent performance as follows. That is, the copolymer emulsion (B) having a high Tg obtained as described above had a low molecular weight of the copolymer and a high tack, because the monomer mixture was emulsified. It is considered that the presence of the tackifier resin during polymerization caused the polymerization of the monomer mixture to be appropriately inhibited.
- the tackifying resin when included during emulsion polymerization, the tackifying resin can be uniformly dissolved or dispersed in the copolymer emulsion (B), so that the tackifying resin is added in the form of an emulsion. It becomes possible to make it contain more.
- the emulsion-type pressure-sensitive adhesive composition of the present invention combined with these, has improved adhesive strength, and has made it possible to realize a pressure-sensitive adhesive that has not been obtained by conventional techniques. thinking. Below, each component etc. which comprise the emulsion type adhesive composition of this invention are demonstrated in detail.
- the emulsion-type pressure-sensitive adhesive composition of the present invention is a copolymer emulsion containing at least 51 to 90% by mass of a low-Tg acrylic pressure-sensitive adhesive emulsion (A) as a main component and a high-Tg tackifying resin as an auxiliary component. It contains at least a mixture of the above two emulsions containing (B) in a proportion of 10 to 49% by mass.
- (A) is contained in a proportion of 60 to 80% by mass
- (B) is contained in a proportion of 20 to 40% by mass.
- the solid content is 50% or more, for example, the solid content is about 60%, the viscosity at 25 ° C.
- the acrylic pressure-sensitive adhesive emulsion (A) as a main component constituting the present invention has a glass transition temperature (Tg) of ⁇ 70 ° C. to ⁇ 50 ° C., which is lower than the copolymer emulsion (B). Further, the viscosity of the emulsion (A) at 25 ° C. is preferably in the range of 50 to 700 mPa ⁇ s.
- the secondary component high-Tg copolymer emulsion (B) mixed with the emulsion (A) at the above-mentioned specific ratio is at least a (meth) acrylic acid alkyl ester in the presence of a specific amount of tackifying resin.
- This is an emulsion of a copolymer obtained by emulsion polymerization of a monomer mixture containing a system monomer, and this configuration makes it possible to realize the remarkable effects of the present invention described above.
- the secondary component high-Tg copolymer emulsion (B) has an adhesion of 20 to 200 parts by mass to 100 parts by mass of a monomer mixture containing at least a (meth) acrylic acid alkyl ester monomer.
- the pressure-sensitive adhesive composition of the present invention is a (meth) acrylic acid alkyl ester monomer in which the amount of the tackifying resin used in the emulsion polymerization of the copolymer emulsion (B) is a polymerization component. More preferably, it is in the range of 40 to 120 parts by mass with respect to 100 parts by mass of the monomer mixture to be included, and the molecular weight of the copolymer is 5000 to 60000. Further, the high Tg copolymer emulsion (B) preferably has a viscosity at 25 ° C. of 50 to 1000 mPa ⁇ s.
- each component constituting the emulsion-type pressure-sensitive adhesive composition of the present invention will be described.
- the emulsion-type pressure-sensitive adhesive composition of the present invention comprises the acrylic pressure-sensitive adhesive emulsion (A) as a main component and 51 to 90% by mass. More preferably, the acrylic pressure-sensitive adhesive emulsion (A) is contained in an amount of 60 to 80% by mass. Further, the acrylic pressure-sensitive adhesive emulsion (A) constituting the present invention needs to have a Tg of ⁇ 70 ° C. to ⁇ 50 ° C., which is lower than the Tg of the copolymer emulsion (B) used in combination. Any known acrylic adhesive emulsion satisfying the glass transition temperature can be used.
- the Tg of the copolymer was calculated from the calculated value using the Tg value of each homopolymer described in the Japan Emulsion Industry Association Standard “Method for Displaying the Hardness of Synthetic Resin Emulsion Films (107-1996)”. Can be sought. This point will be described later.
- the acrylic pressure-sensitive adhesive emulsion (A) has a (co) polymer satisfying the Tg range obtained by emulsion polymerization of an acrylic monomer such as (meth) acrylic acid or (meth) acrylic acid ester. Anything is acceptable.
- an acrylic monomer such as (meth) acrylic acid or (meth) acrylic acid ester. Anything is acceptable.
- the acrylic monomer for example, the following (meth) acrylic acid alkyl ester monomers can be easily obtained either alone or by emulsion polymerization of two or more kinds.
- Examples of the (meth) acrylic acid alkyl ester monomer that can be used for the preparation of the emulsion (A) include methyl (meth) acrylate, ethyl (meth) acrylate, n-propyl (meth) acrylate, isopropyl (meth) ) Acrylate, n-butyl (meth) acrylate, isobutyl (meth) acrylate, sec-butyl (meth) acrylate, t-butyl (meth) acrylate, hexyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, octyl (meth) ) Acrylate, n-nonyl (meth) acrylate, isononyl (meth) acrylate, decyl (meth) acrylate, undecyl (meth) acrylate, dodecyl (meth) acrylate, n-a
- the emulsion (A) constituting the present invention can be prepared by using one or more of the above-mentioned monomers, and is particularly selected from acrylic acid esters having an alkyl chain having 4 to 12 carbon atoms. It is preferable to use a monomer as a main component.
- the acrylic pressure-sensitive adhesive emulsion (A) can be prepared in addition to the above monomers, as well as other acrylic monomers and copolymerizable monomers other than the acrylic monomers as listed below.
- Meters can also be used.
- vinyl monomers such as acrylonitrile, vinyl acetate, vinyl propionate or vinyl versatate, styrene, vinyl benzoate and the like can be mentioned.
- Examples thereof include monomers containing two or more polymerizable unsaturated groups. And from these groups, 1 or more types can be used as needed.
- unsaturated monomers having various functional groups as listed below can also be used as monomers in preparing the acrylic pressure-sensitive adhesive emulsion (A) constituting the present invention.
- examples thereof include unsaturated monomers having a carboxyl group, an amide group or a substituted amide group, an amino group or a substituted amino group, a hydroxyl group, an epoxy group, a carbonyl group, a mercapto group, or a silicon-containing group.
- an unsaturated monomer having a carboxyl group, a hydroxyl group, a carbonyl group, or an epoxy group is used, and one or more of these groups can be used as necessary.
- Examples of the unsaturated monomer having a carboxyl group include (meth) acrylic acid, itaconic acid, maleic acid, maleic anhydride, fumaric acid, fumaric anhydride and the like.
- Examples of the unsaturated monomer having a hydroxyl group include 2-hydroxyethyl (meth) acrylate, 4-hydroxypropyl (meth) acrylate, 2-hydroxybutyl (meth) acrylate, caprolactone-modified (meth) acrylate, polyethylene glycol ( Examples thereof include (meth) acrylate and polypropylene glycol (meth) acrylate.
- Examples of the unsaturated monomer having a carbonyl group include acrolein, diacetone acrylamide, formyl styrene, vinyl methyl ketone, vinyl ethyl ketone, (meth) acrylooxyalkylpropenal, diacetone (meth) acrylate, acetonyl (meth) ) Acrylate, acetoacetoxyethyl (meth) acrylate, and the like.
- Examples of the unsaturated monomer having an epoxy group include glycidyl (meth) acrylate, glycidyl (meth) allyl ether, 3,4-epoxycyclohexyl (meth) acrylate, and the like.
- the acrylic pressure-sensitive adhesive emulsion (A) constituting the emulsion-type pressure-sensitive adhesive composition of the present invention is copolymerized, the resulting emulsion is constituted from calculated values obtained using the Tg values of the respective homopolymers.
- Emulsion polymerization is performed by designing the monomer composition by appropriately selecting the monomers listed above so that the Tg of the copolymer to be in the range of ⁇ 70 ° C. to ⁇ 50 ° C.
- the emulsion polymerization method performed at this time is not particularly limited, and can be appropriately produced using a conventionally known emulsion polymerization method. For example, it can be produced by any one of a one-stage polymerization method, a multi-stage polymerization method, or a combination thereof.
- the specific method of emulsion polymerization is not particularly limited, but the following methods can be used.
- an acrylic monomer component such as the above-mentioned (meth) acrylic acid alkyl ester monomer alone or a monomer mixture containing a plurality of components is reacted with at least water, a surfactant and a polymerization initiator.
- Emulsion polymerization method single monomer or monomer mixture emulsified with water and surfactant in advance, in water and, if necessary, reaction vessel charged with surfactant and polymerization initiator Examples thereof include a method of performing emulsion polymerization by dropping, a method using a combination thereof, and the like.
- Polymerization initiator As the polymerization initiator used in the above emulsion polymerization, for example, an ammonium salt peroxide such as ammonium persulfate, an organic peroxide such as t-butyl hydroperoxide, hydrogen peroxide, or the like can be used.
- the amount of these polymerization initiators used is about 0.1 to 1.0 part by mass per 100 parts by mass of a single monomer or monomer mixture used in producing the acrylic pressure-sensitive adhesive emulsion (A). It is preferable to do.
- the polymerization initiator can be used in each stage of polymerization, and a predetermined amount can be added in each stage to carry out the polymerization reaction.
- a surfactant in the above emulsion polymerization, can be used as an emulsifier.
- any conventionally known anionic surfactant, nonionic surfactant, etc. may be used. it can.
- a surfactant having at least one hydrophilic group selected from —SO 3 NH 4 group, —OSO 2 NH 4 group, or ethylene oxide chain may be used.
- anionic surfactant examples include New Coal 707SF, New Coal 714SF, New Coal 723SF, and New Coal 740SF [both trade names, manufactured by Nippon Emulsifier Co., Ltd.].
- Specific nonionic surfactants that can be used in the present invention include, for example, New Coal 707, New Coal 710, New Coal 714, New Coal 723, New Coal 740, and New Coal 780 (both trade names, Nippon Emulsifier Co., Ltd.).
- the surfactant used in the present invention is more preferably a reactive surfactant having a polymerizable ethylenically unsaturated group.
- examples of such include sodium polyoxyethylene alkyl ether sulfate.
- LATEMUL E-118B, LATEMUL PD-104, LATEMUL PD-105, LATEMUL PD-420, LATEMUL PD-430, LATEMUL PD-430S and LATEMUL PD-450 [all trade names, manufactured by Kao Corporation , Aqualon HS-10, Aqualon KH-05, Aqualon KH-10, Aqualon RN-05, Aqualon RN-10 and Aqualon RN-20 [all trade names, manufactured by Daiichi Kogyo Seiyaku Co., Ltd.]
- Rear soap SE-10N Adekaria soap SR-10, Adekaria soap SR-20, Adekaria soap SR-3025, Adekaria soap ER-10, Adekaria soap ER-20, Adek
- the amount of the surfactant used as described above when the acrylic pressure-sensitive adhesive emulsion (A) constituting the emulsion-type pressure-sensitive adhesive composition of the present invention is obtained by emulsion polymerization is a single amount used for polymerization. It is preferably 0.1 to 5 parts by mass with respect to 100 parts by mass of the body or monomer mixture. If the amount of the surfactant used is less than 0.1 parts by mass, the resulting emulsion (A) tends to be inferior in polymerization stability, such being undesirable. On the other hand, when the amount of the surfactant used is more than 5 parts by mass, a pressure-sensitive adhesive layer is formed on the adherend using the pressure-sensitive adhesive composition of the present invention obtained by mixing the obtained emulsion (A). In some cases, the properties of the pressure-sensitive adhesive layer do not tend to be sufficiently good.
- the acrylic pressure-sensitive adhesive emulsion (A) constituting the present invention obtained as described above has a glass transition temperature (Tg) of ⁇ 70 ° C. to ⁇ 50 ° C. and a low Tg. Is required. More preferably, it is ⁇ 70 to ⁇ 60 ° C. When Tg is lower than ⁇ 70 ° C., the cohesive force is low and the paste sticking out and die cutting properties are poor. When it is higher than ⁇ 50 ° C., high tack may be difficult to obtain.
- Tg glass transition temperature
- the acrylic pressure-sensitive adhesive emulsion (A) constituting the present invention may be any as long as the Tg is in the above-mentioned range, but more preferably satisfies the following physical properties.
- the viscosity at 25 ° C. is preferably about 50 to 700 mPa ⁇ s, more preferably 50 to 300 mPa ⁇ s. That is, when the viscosity is out of the above range, the finally obtained emulsion-type pressure-sensitive adhesive composition of the present invention has a viscosity at 25 ° C. of 1000 mPa ⁇ s or less, more preferably 500 mPa ⁇ s or less. This is not preferable because it may be difficult.
- the acrylic pressure-sensitive adhesive emulsion (A) constituting the present invention preferably has an average particle size of about 70 to 500 nm. If the particle diameter is out of the above range, there may be a case where the stability of the particles is poor and the emulsion is separated or settled.
- the acrylic pressure-sensitive adhesive emulsion (A) constituting the present invention preferably has a gel fraction of about 40 to 80%. If the gel fraction is outside the above range, the cohesive force may be insufficient or the tack may be low.
- the copolymer emulsion (B) constituting the emulsion-type pressure-sensitive adhesive composition of the present invention is a copolymer obtained by emulsion polymerization of at least a (meth) acrylic acid alkyl ester monomer in the presence of a tackifier resin. It is a polymer emulsion.
- the content of the copolymer emulsion (B) which is a subcomponent of the emulsion-type pressure-sensitive adhesive composition of the present invention is in the range of 10 to 49% by mass, but is mixed in the range of 20 to 40% by mass. Is more preferable.
- the (meth) acrylic acid alkyl ester monomer used for obtaining the copolymer emulsion (B) constituting the present invention is the same as previously described in the description of the acrylic adhesive emulsion (A). Any of these can be used.
- the monomer mixture of the (meth) acrylic acid alkyl ester monomers listed in the description of the emulsion (A), or the (meth) Acrylic acid alkyl ester monomers other acrylic monomers as described above, monomers other than acrylic monomers, and unsaturated monomers having various functional groups as described above
- a monomer mixture in which the body (hereinafter referred to as “other copolymerizable monomer”) is used in combination can be used. For this reason, the description about the monomer which can be used is abbreviate
- the emulsion (B) can be obtained by copolymerizing a monomer mixture using at least a monomer containing a (meth) acrylic acid alkyl ester monomer from the monomers described above. As the production method at that time, the same method as that for producing the emulsion (A) can be used. Therefore, description of this point is also omitted. However, when designing the monomer mixture for obtaining the copolymer emulsion (B), it is necessary to make the Tg of the copolymer obtained by emulsion polymerization to be ⁇ 30 ° C. to 30 ° C. is there. This point will be described later.
- the amount used is, for example, a ratio of 0.1 to 70% by mass in 100% by mass of all the components of the monomer for forming the copolymer emulsion (B). It is preferably used in the range of about 0.1 to 50% by mass.
- Tackifying resin When the copolymer emulsion (B) having a high Tg constituting the present invention is obtained by emulsion polymerization of the monomer mixture as described above, a (meth) acrylic acid alkyl ester-based monomer is present in the presence of a tackifier resin. It is characterized by emulsion polymerization of a monomer having at least a monomer. That is, in the present invention, the high-Tg copolymer emulsion (B), which is a subcomponent, is used instead of the presence of a tackifying resin in the production of the main component, low-Tg acrylic pressure-sensitive adhesive emulsion (A).
- a tackifying resin is present in the preparation obtained by emulsion polymerization.
- the tack of the copolymer emulsion (B) having a high holding power and a low tack, and a high Tg can be increased, and more tackifying resin can be contained. Therefore, in the pressure-sensitive adhesive of the present invention, it is possible to realize a sufficiently high adhesive force and a high tack. Furthermore, the remarkable effect of this invention is achieved by making the copolymer which comprises an emulsion (B) the thing of the specific property prescribed
- the copolymer emulsion (B) is a composite of the emulsion and the tackifier resin in a good state by being configured in this way. Even when (B) is mixed with the low-Tg acrylic pressure-sensitive adhesive emulsion (A), which is the main component described above, to make the emulsion-type pressure-sensitive adhesive composition of the present invention, the tackifying resin is good. The dissolved or dispersed state is maintained.
- the tackifier resin when a tackifier resin is present when preparing by emulsion polymerization of a monomer mixture containing at least a (meth) acrylic acid alkyl ester monomer, the monomer When the tackifier resin is dissolved or dispersed in the mixture and the monomer mixture is emulsion polymerized in that state, the tackifier resin can be uniformly dissolved or dispersed in the resulting copolymer emulsion (B). it can.
- the emulsion-type pressure-sensitive adhesive composition of the present invention comprises a high-Tg copolymer emulsion (B) prepared as described above, in which a tackifying resin is uniformly dissolved or dispersed, and a low-Tg acrylic as a main component.
- a tackifying resin is uniformly dissolved or dispersed
- a low-Tg acrylic as a main component.
- the present invention contains a mixture of two emulsions, a low Tg acrylic adhesive emulsion (A) and a high Tg copolymer emulsion (B).
- a low Tg acrylic adhesive emulsion A
- a high Tg copolymer emulsion B
- emulsion polymerization is carried out without the presence of a tackifying resin, and it is used in the pressure-sensitive adhesive of the present invention. Even if a tackifying resin similar to that described above is added later in the form of an emulsion, the above-described remarkable effects of the present invention cannot be obtained.
- the viscosity of the pressure-sensitive adhesive composition at 25 ° C. is as low as 1000 mPa ⁇ s or less, the post-added tackifying resin is separated or the tackifying resin is precipitated over time, It is not an excellent emulsion-type pressure-sensitive adhesive composition as achieved in the present invention.
- the monomer when producing a low Tg acrylic adhesive emulsion (A) as a main component, the monomer is used alone or a mixture of two or more monomers.
- An emulsion-type pressure-sensitive adhesive composition can be provided.
- the tackifying resin is not particularly limited as long as it can be dissolved or dispersed in a mixture of monomers, and any conventionally known one can be used.
- tackifying resins include rosin resins, polyterpene resins, coumarone indene resins, phenol resins, xylene resins, aliphatic petroleum resins, aromatic petroleum resins, and the like.
- the rosin resin include natural rosin, rosin ester, hydrogenated rosin, hydrogenated rosin ester, polymerized rosin, polymerized rosin ester, disproportionated rosin, and disproportionated rosin ester.
- the polyterpene resin include ⁇ -pinene resin, ⁇ -pinene resin, and terpene phenol resin.
- the hydrogenated petroleum resin etc. of an aliphatic petroleum resin or an aromatic petroleum resin are mentioned.
- tackifying resin used in the present invention among the above-mentioned tackifying resins, those having a softening point (° C.) of 70 ° C. to 170 ° C. are preferable.
- Specific examples of the tackifying resin having a softening point within the above range include, for example, Pencel D-125 (trade name, manufactured by Arakawa Chemical Industries, Ltd.), which is a polymerized rosin ester having a softening point of 125 ° C., and a softening point of 150.
- Pencel D-160 (trade name, manufactured by Arakawa Chemical Co., Ltd.) which is a polymerized rosin ester at °C
- PINEREZ 2410 (trade name, manufactured by LAWTER) which is a rosin ester having a softening point of 100 ° C
- a terpene resin having a softening point of 115 ° C examples thereof include YS resin PX1150 (trade name, manufactured by Yasuhara Chemical Co., Ltd.), YS Polystar T160 (trade name, manufactured by Yasuhara Chemical Co., Ltd.) which is a terpene phenol resin having a softening point of 160 ° C.
- the amount of the tackifying resin used is 20 to 200 parts by mass, and further 40 to 120 parts by mass with respect to 100 parts by mass of the monomer mixture used in the emulsion polymerization of the copolymer emulsion (B). It is preferable.
- the amount used is less than 20 parts by mass, the high-Tg copolymer emulsion (B) is mixed with the low-Tg acrylic pressure-sensitive adhesive emulsion (A) as the main component, and the emulsion-type pressure-sensitive adhesive composition of the present invention.
- the copolymer emulsion (B) can also be appropriately produced by a conventionally known emulsion polymerization method.
- the emulsion polymerization method include a single-stage polymerization method, a multi-stage polymerization method, and a combination thereof, and any of them can be used. Since the polymerization initiator and the surfactant that can be used in the above polymerization can be the same as those that can be used in the production of the acrylic pressure-sensitive adhesive emulsion (A) described above, the description thereof is omitted.
- the copolymer emulsion (B) constituting the present invention obtained as described above has a glass transition temperature (Tg) higher than that of the emulsion (A) used in combination as described above, and is ⁇ 30 ° C. to 30 ° C. It is necessary to be. Further, a temperature of about ⁇ 20 to 20 ° C. is more preferable.
- Tg of a copolymer emulsion (B) can be calculated
- the copolymer emulsion (B) constituting the present invention is required to have a molecular weight of 5000 to 70000.
- a monomer mixture emulsion polymerization containing a (meth) acrylic acid alkyl ester monomer is carried out in the presence of a tackifier resin, the molecular weight of the resulting copolymer becomes small.
- the copolymer emulsion (B) having a high Tg as defined in the present invention as a secondary component it becomes a property that can realize a sufficiently high adhesive force and high tack.
- the molecular weight is 100,000 or more, and the remarkable effects of the present invention are not realized.
- the copolymer emulsion (B) constituted as described above has a gel fraction of 20% or less. According to the study by the present inventors, when the gel fraction exceeds 20%, in the pressure-sensitive adhesive layer formed by using the pressure-sensitive adhesive composition obtained by mixing the emulsion (B), sufficient high adhesive strength and High tack cannot be realized. Although it is possible to prescribe
- the copolymer emulsion (B) constituting the present invention needs to have an average particle size of 200 to 2000 nm, and more preferably 200 to 1000 nm.
- the average particle diameter is smaller than 200 nm, the mixture may be aggregated when mixed with the acrylic pressure-sensitive adhesive emulsion (A) to obtain an emulsion-type pressure-sensitive adhesive composition.
- the average particle size is larger than 2000 nm, separation occurs when the emulsion-type pressure-sensitive adhesive composition is allowed to stand.
- the copolymer emulsion (B) preferably has a viscosity at 25 ° C. of about 50 to 1000 mPa ⁇ s, and more preferably 50 to 500 mPa ⁇ s. If the viscosity is outside the above range, it may be difficult to make the finally obtained emulsion-type pressure-sensitive adhesive composition of the present invention 1000 mPa ⁇ s or less, which is not preferable.
- the emulsion-type pressure-sensitive adhesive composition of the present invention contains the above-mentioned low-Tg acrylic pressure-sensitive adhesive emulsion (A) as a main component, and its content is in the range of 51 to 90% by mass, preferably 60 to 80% by mass.
- the high-Tg copolymer emulsion (B) having the above-mentioned specific properties is used as a subcomponent, and the content thereof is 10 to 49% by mass, preferably 20 to 40% by mass.
- the emulsion-type pressure-sensitive adhesive composition of the present invention is a mixture of a low Tg acrylic pressure-sensitive adhesive emulsion (A) as a main component and a high Tg copolymer emulsion (B) as a subcomponent at the above ratio.
- A low Tg acrylic pressure-sensitive adhesive emulsion
- B high Tg copolymer emulsion
- the emulsion-type pressure-sensitive adhesive composition of the present invention requires that the viscosity at 25 ° C. is as low as 1000 mPa ⁇ s or less as measured by a B-type viscometer. In order to further improve the viscosity, the viscosity at 25 ° C. is preferably about 50 to 700 mPa ⁇ s, and more preferably about 500 mPa ⁇ s.
- the emulsion-type pressure-sensitive adhesive composition of the present invention has a viscosity at a shear rate of 10 4 s ⁇ 1 at 25 ° C. of 200 mPa ⁇ s or less, more preferably 100 mPa ⁇ s or less, as measured by a rheometer.
- the emulsion-type pressure-sensitive adhesive composition of the present invention has a low viscosity as described above, it is possible to reduce the amount of pressure-sensitive adhesive applied when used, and it is economical and forms a pressure-sensitive adhesive layer. Since it is possible to perform coating at a high speed, a remarkable effect can be obtained that the working efficiency can be improved. Furthermore, the emulsion-type pressure-sensitive adhesive composition of the present invention has an excellent performance capable of forming a pressure-sensitive adhesive layer having high adhesive force and high tack while being the above-described low-viscosity pressure-sensitive adhesive.
- the viscosity of the emulsion-type pressure-sensitive adhesive composition of the present invention may be adjusted using a conventionally known thickener. This is a preferred form.
- Tg (° C.) The glass transition temperature Tg (° C.) of each emulsion composed of the copolymer used in Examples and Comparative Examples was determined by the following formula.
- Formula: 1 / (Tg + 273) ⁇ [Wn / (Tg n +273)] (In the above formula, Tg (° C.) represents the glass transition temperature of the copolymer, Wn represents the weight fraction of each monomer, and Tg n (° C.) represents the glass transition temperature of the homopolymer of each monomer, n Represents the type of each monomer.)
- Tg n The glass transition temperature Tg n (° C.) of the homopolymer of each monomer used in the case, respectively using literature values described below.
- Styrene 100 ° C
- the monomer emulsion used above is a monomer mixture of 69 parts of 2-ethylhexyl acrylate (abbreviated as 2-EHA), 30 parts of butyl acrylate (abbreviated as BA) and 1 part of acrylic acid (abbreviated as AAC).
- 2-EHA 2-ethylhexyl acrylate
- BA butyl acrylate
- AAC acrylic acid
- 4 parts of sodium polyoxyethylene alkyl ether sulfate (trade name: Latemul E-118B, manufactured by Kao Corporation) and 30 parts of ion-exchanged water were mixed and emulsified.
- 4 parts of an aqueous 5% ammonium persulfate solution was dropped. After completion of dropping, the mixture was aged at 80 ° C.
- the gel fraction of the emulsion was measured as follows.
- the emulsion was coated on a polyramidone separator so as to be 20 g / m 2 / dry, and dried for 60 seconds with a 120 ° C. drier.
- 1 g of the obtained film sample was immersed in 500 g of toluene for 24 hours.
- the filtered residue is dried at 90 ° C. for 3 hours with a hot air dryer, and left in a desiccator for 24 hours, and then the weight of the remaining film is measured.
- the gel fraction was calculated from the change.
- the average particle size of the emulsion was measured with a laser diffraction particle size distribution analyzer SALD-7100 (manufactured by Shimadzu Corporation).
- the weight average molecular weight of the soluble tetrahydrofuran in the dried film was measured by GPC (Gel Permeation Chromatography) using polystyrene as a standard substance.
- the monomer emulsion used above was 49 parts of 2-ethylhexyl acrylate, 10 parts of methyl methacrylate (abbreviated as MMA), 40 parts of styrene (abbreviated as ST), 1 part of acrylic acid, and tackifier (tackifier resin).
- Rosin resin Arakawa Chemical Industries, Ltd., trade name: Pencel D-125
- monomer mixture polyoxyethylene alkyl ether sodium sulfate
- Latemul E-118B trade name: Latemul E-118B
- AB-1 is obtained by emulsion polymerization by adding a tackifier to a low Tg monomer and a high Tg monomer, and is completely different from the structure defined in the present invention.
- Examples 1 to 10 and Comparative Examples 1 to 11 The acrylic adhesive emulsions (A-1) to (A-3) obtained in Synthesis Example 1 and Comparative Synthesis Examples 1 and 2 were obtained in Synthesis Examples 2 to 7 and Comparative Synthesis Examples 3 to 8. Copolymer emulsions (B-1) to (B-12) are used and blended in the combinations and proportions shown in Tables 4-1 and 4-2, and the viscosity is adjusted to about 500 mPa ⁇ s with a thickener. By doing this, the emulsion type adhesive composition of the Example of this invention and the comparative example was obtained, respectively.
- the emulsion-type pressure-sensitive adhesive composition of Comparative Example 7 was obtained using the copolymer emulsion (AB-1) obtained in Comparative Synthesis Example 9 described above.
- AB-1 copolymer emulsion obtained in Comparative Synthesis Example 9
- Superester E-730-55 (trade name, viscosity: 40 mPa ⁇ s, average particle size: 500 nm, specific gravity: 1.05) manufactured by Arakawa Chemical Industries, Ltd. was used.
- the acrylic adhesive emulsion of Example 1 prepared as described above the viscosity at a shear rate of 10 4 s ⁇ 1 with a rheometer measured by the following method was 100 mPa ⁇ s.
- Viscosity measurement with a rheometer was performed as follows. Viscoelasticity measuring apparatus Physica MCR301 (manufactured by Anton Paar) was used to measure the viscosity up to a shear rate of 10 4 s ⁇ 1 at 25 ° C. using a cone plate.
- Comparative Examples 8 and 9 The pressure-sensitive adhesive compositions of Comparative Examples 8 and 9 were prepared by using the acrylic pressure-sensitive adhesive emulsions A-2 and A-3 prepared in Comparative Synthesis Examples 1 and 2, respectively, as a copolymer emulsion (B) used in combination. A pressure-sensitive adhesive composition was prepared in the same manner as in Example 4 using the copolymer emulsion (B-4) specified in the present invention prepared in Synthesis Example 5.
- Comparative Examples 10 and 11 The pressure-sensitive adhesive compositions of Comparative Examples 10 and 11 are the acrylic pressure-sensitive adhesive emulsion (A-1) defined in the present invention obtained in Synthesis Example 1 and the copolymer emulsion defined in the present invention prepared in Synthesis Example 5. (B-4) is used, and the usage ratio of both is out of the range defined in the present invention.
- ⁇ Performance test> (Preparation of test samples) Each emulsion-type pressure-sensitive adhesive composition of Examples and Comparative Examples was applied on a polyramidone separator so as to be 20 g / m 2 / dry, dried for 60 seconds with a 120 ° C. drier, and then on the pressure-sensitive adhesive layer. High quality paper (64 g / m 2 ) was bonded and left in a 23 ° C., 50% RH atmosphere for 16 hours or more to prepare an adhesive sheet, which was used as a test sample. A plurality of the test samples were prepared under the same conditions and used for the following tests.
- the pressure-sensitive adhesive layers formed using the pressure-sensitive adhesive compositions of the Examples all have a high adhesive strength of 15 N / 25 mm or more, and all have a loop tack of 13 N / It was confirmed that the tackiness was as high as 25 mm or more and the liquid stability was excellent.
- the pressure-sensitive adhesive layer formed using the pressure-sensitive adhesive composition of Comparative Example is not sufficient in the pressure-sensitive adhesive force and tack of the pressure-sensitive adhesive compositions of Comparative Examples 1 to 3 and 7, and the copolymer emulsion (B ),
- the pressure-sensitive adhesive composition of Comparative Example 4 using a material having an average particle size smaller than that defined in the present invention agglomerated, and the adhesive strength and tack could not be measured.
- Table 5 the pressure-sensitive adhesive compositions of Comparative Example 6 and Comparative Example 7 to which no tackifying resin was present during the emulsion polymerization and the commercially available tackifier emulsion were added were separated. As a result, liquid stability was poor.
- the pressure-sensitive adhesive compositions of Comparative Examples 8 and 9 were prepared by using the acrylic pressure-sensitive adhesive emulsions A-2 and A-3 prepared in Comparative Synthesis Examples 1 and 2, respectively, as a copolymer emulsion (B) used in combination.
- a pressure-sensitive adhesive composition was produced in the same manner as in Example 2 using the copolymer emulsion B-4 produced in Synthesis Example 5.
- these pressure-sensitive adhesive compositions did not have high adhesive strength and high-tack pressure-sensitive adhesive performance like the pressure-sensitive adhesive composition of Example 4.
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Abstract
Description
本発明のエマルション型粘着剤組成物は、アクリル系粘着剤エマルション(A)をその主成分とし、51~90質量%含有してなる。アクリル系粘着剤エマルション(A)を60~80質量%含有するものであることがより好ましい。また、本発明を構成するアクリル系粘着剤エマルション(A)は、そのTgが、併用する共重合体エマルション(B)のTgよりも低い、-70℃~-50℃であることを要する。上記ガラス転移温度を満たすアクリル系の粘着剤エマルションであれば、従来公知のものをいずれも使用することができる。なお、共重合体のTgについては、日本エマルジョン工業会規格「合成樹脂エマルジョンの皮膜の硬さ表示方法(107-1996)」に記載された、各ホモポリマーのTg値を使用して計算値から求めることができる。この点については後述する。
上記アクリル系粘着剤エマルション(A)は、(メタ)アクリル酸や(メタ)アクリル酸エステル等のアクリル系単量体を乳化重合してなる、上記Tgの範囲を満たす(共)重合体を有するものであればよい。アクリル系単量体としては、例えば、下記に挙げるような(メタ)アクリル酸アルキルエステル系単量体を、単独で或いは2種以上を乳化重合することによって容易に得られる。エマルション(A)の調製に用いることのできる(メタ)アクリル酸アルキルエステル系単量体としては、例えば、メチル(メタ)アクリレート、エチル(メタ)アクリレート、n-プロピル(メタ)アクリレート、イソプロピル(メタ)アクリレート、n-ブチル(メタ)アクリレート、イソブチル(メタ)アクリレート、sec-ブチル(メタ)アクリレート、t-ブチル(メタ)アクリレート、ヘキシル(メタ)アクリレート、2-エチルヘキシル(メタ)アクリレート、オクチル(メタ)アクリレート、n-ノニル(メタ)アクリレート、イソノニル(メタ)アクリレート、デシル(メタ)アクリレート、ウンデシル(メタ)アクリレート、ドデシル(メタ)アクリレート、n-アミル(メタ)アクリレート、イソアミル(メタ)アクリレート、ベンジル(メタ)アクリレート、ラウリル(メタ)アクリレート、シクロヘキシル(メタ)アクリレート、テトラデシル(メタ)アクリレート、ステアリル(メタ)アクリレート、2-メトキシエチルアクリレート及びエチルカルビトールアクリレート等が挙げられる。本発明を構成するエマルション(A)は、上記に挙げた単量体の群より1種以上使用することで調製できるが、特に、炭素数4~12のアルキル鎖を有するアクリル酸エステルから選ばれた単量体を主成分として使用することが好ましい。
本発明のエマルション型粘着剤組成物を構成するアクリル系粘着剤エマルション(A)を共重合して得る場合は、各ホモポリマーのTg値を使用して得た計算値から、得られるエマルションを構成する共重合体のTgが-70℃~-50℃の範囲内になるように、上記に挙げたような単量体を適宜に選択してモノマー組成を設計し、乳化重合する。この際に行う乳化重合方法は特に限定されず、従来公知の乳化重合方法を利用して適宜に製造することができる。例えば、1段重合方法、多段重合方法、または、これらの組み合わせによる方法の、いずれの方法でも製造することができる。
上記した乳化重合の際に用いる重合開始剤としては、例えば、過硫酸アンモニウム等のアンモニウム塩過酸化物、t-ブチルハイドロパーオキサイド、過酸化水素等の有機過酸化物等を使用できる。これらの重合開始剤の使用量は、アクリル系粘着剤エマルション(A)を製造する際に用いる、単独単量体或いは単量体混合物100質量部あたり、0.1~1.0質量部程度とすることが好ましい。また、重合開始剤は、重合の各段階で用いることができ、各段階で所定量を添加して、重合反応を行うことができる。
上記した乳化重合の際には、乳化剤として界面活性剤を用いることができる。本発明で規定する共重合体エマルション(B)を得る際に行う乳化重合の際も同様であり、従来公知の陰イオン性界面活性剤、非イオン性界面活性剤等、如何なるものも用いることができる。例えば、-SO3NH4基、-OSO2NH4基、或いは、エチレンオキサイド鎖の中から選ばれた少なくとも1種の、親水基を有する界面活性剤等が挙げられる。具体的な陰イオン性界面活性剤としては、例えば、ニューコール707SF、ニューコール714SF、ニューコール723SF及びニューコール740SF〔共に商品名、日本乳化剤(株)製〕等を使用することができる。また、本発明で使用し得る具体的な非イオン性界面活性剤としては、例えば、ニューコール707、ニューコール710、ニューコール714、ニューコール723、ニューコール740及びニューコール780(共に商品名、日本乳化剤(株)製)等が挙げられる。
上記のようにして得られる本発明を構成するアクリル系粘着剤エマルション(A)は、先述したように、そのガラス転移温度(Tg)が、-70℃~-50℃と、低Tgであることを必須とする。より好ましくは、-70~-60℃であることが好ましい。Tgが、-70℃よりも低いと、凝集力が低く、糊のはみ出しやダイカット性に劣り、-50℃より高いと、高タックが得られ難い場合がある。
次に、上記した主成分である低Tgのアクリル系粘着剤エマルション(A)に混合して用いられる、(A)よりもTgが高い、副成分である高Tgの共重合体エマルション(B)について説明する。本発明のエマルション型粘着剤組成物を構成する共重合体エマルション(B)は、粘着付与樹脂の存在下、少なくとも(メタ)アクリル酸アルキルエステル系単量体を乳化重合することにより得られた共重合体のエマルションである。更に、(メタ)アクリル酸アルキルエステル系単量体を含む単量体混合物100質量部に、20~200質量部の粘着付与樹脂を存在させて乳化重合してなるものであり、且つ、そのTgが-30℃~30℃であり、その分子量が5000~70000であり、更に、共重合体の平均粒子径が200~2000nmの共重合体エマルションである。このように構成したことで、上記共重合体のゲル分率は20%以下と小さくなるが、0であってもよい。本発明のエマルション型粘着剤組成物の副成分である共重合体エマルション(B)の含有量は、10~49質量%の範囲内であるが、20~40質量%の範囲内で混合することがより好ましい。
本発明を構成する共重合体エマルション(B)を得る際に用いる、(メタ)アクリル酸アルキルエステル系単量体には、先にアクリル系粘着剤エマルション(A)の説明で示したと同様のものをいずれも使用することができる。すなわち、エマルション(B)を製造する際には、エマルション(A)の説明の際に列記した前記の(メタ)アクリル酸アルキルエステル系単量体の単量体混合物で、或いは、前記(メタ)アクリル酸アルキルエステル系単量体と共に、前記したその他のアクリル系単量体や、アクリル系単量体以外の共重合可能な単量体、及び、前記した種々の官能基を有する不飽和単量体(以下、「その他の共重合可能な単量体」と呼ぶ。)を併用した単量体混合物を使用することができる。このため、使用できる単量体についての説明は省略する。また、エマルション(B)は、上記した単量体の中から、少なくとも(メタ)アクリル酸アルキルエステル系単量体を含む単量体を併用した単量体混合物を共重合することで得られるが、その際の製造方法は、エマルション(A)を製造する際の方法と同様のものが利用できる。よって、この点についても説明を省略する。但し、共重合体エマルション(B)を得るための単量体混合物を設計する際には、乳化重合して得られる共重合体のTgが、-30℃~30℃となるようにする必要がある。この点については後述する。
本発明を構成する高Tgの共重合体エマルション(B)は、上記したような単量体混合物を乳化重合して得る際に、粘着付与樹脂の存在下、(メタ)アクリル酸アルキルエステル系単量体を少なくとも有する単量体を乳化重合させてなることを特徴とする。すなわち、本発明では、主成分である低Tgのアクリル系粘着剤エマルション(A)の製造の際に粘着付与樹脂を存在させるのでなく、副成分となる高Tgの共重合体エマルション(B)を乳化重合して得る調製時に、粘着付与樹脂を存在させる。このような構成としたことで、通常は、保持力が高くタックが低い、高Tgの共重合体エマルション(B)のタックを高めることができ、更に、粘着付与樹脂を多く含有させることができるので、本発明の粘着剤において、十分な高粘着力と高タックの実現が可能になる。更に、エマルション(B)を構成する共重合体を本発明で規定する特定の性状のものとしたことで、本発明の顕著な効果を達成する。すなわち、本発明者らの検討によれば、このように構成したことで、共重合体エマルション(B)は、エマルションと粘着付与樹脂とが良好な状態に複合化したものとなり、更に、該エマルション(B)を、先に説明した主成分である低Tgのアクリル系粘着剤エマルション(A)に混合して、本発明のエマルション型粘着剤組成物にした場合にも、粘着付与樹脂の良好な溶解或いは分散状態が保たれる。
共重合体エマルション(B)も、アクリル系粘着剤エマルション(A)と同様に、従来公知の乳化重合方法によって適宜に製造することができる。乳化重合方法としては、例えば、1段重合方法、多段重合方法、または、これらの組み合わせによる方法があるが、いずれも使用することができる。上記重合において使用可能な重合開始剤や界面活性剤は、先に記載したアクリル系粘着剤エマルション(A)の製造において使用できるものと同じものを使用することができるので、説明を省略する。
上記のようにして得られる本発明を構成する共重合体エマルション(B)は、そのガラス転移温度(Tg)が、先に説明した併用するエマルション(A)よりも高く、-30℃~30℃であることを要する。更には、-20~20℃程度のものがより好ましい。Tgが、-30℃より低い、或いは、30℃よりも高いと、先に説明した低Tgのアクリル系粘着剤エマルション(A)と混合してなる、粘着剤組成物を用いて形成した粘着剤層が、高粘着力と高タックを実現できなくなる。なお、共重合体エマルション(B)のTgは、先に説明したアクリル系粘着剤エマルション(A)を共重合体とした場合と同様の方法で求めることができる。
本発明のエマルション型粘着剤組成物は、上記した低Tgのアクリル系粘着剤エマルション(A)を主成分とし、その含有量が51~90質量%、好ましくは、60~80質量%の範囲であり、上記した特有の性状を有する高Tgの共重合体エマルション(B)を副成分とし、その含有量が10~49質量%、好ましくは、20~40質量%の割合で構成されている。本発明のエマルション型粘着剤組成物は、主成分である低Tgのアクリル系粘着剤エマルション(A)と、副成分である高Tgの共重合体エマルション(B)とを上記の割合で混合してなることで、その液安定性に優れ、また、該エマルション型粘着剤組成物を用いて形成した粘着剤層の粘着性能(高粘着力・高タック)とを、バランスよく達成したものとなる。
式:1/(Tg+273)=Σ〔Wn/(Tgn+273)〕
(上記式中、Tg(℃)は、共重合体のガラス転移温度、Wnは各モノマーの重量分率を表し、Tgn(℃)は、各モノマーによるホモポリマーのガラス転移温度を表し、nは、各モノマーの種類を表す。)
2-エチルヘキシルアクリレート(2EHA):-70℃
ブチルアクリレート(BA):-55℃
メチルメタクリレート(MMA):105℃
イソノニルアクリレート(INA):-85℃
スチレン:100℃
アクリル酸(AAC):106℃
温度計、撹拌機、滴下装置、還流冷却管及び窒素導入管を備えた反応装置に、イオン交換水28部を秤量し、窒素を封入して内温を80℃まで昇温させた。そして、その温度に保ちながら、10%濃度の過硫酸アンモニウム水溶液2部を添加し、直ちに、別に準備しておいた、下記のようにして調製した単量体乳化物を連続的に4時間滴下して乳化重合した。上記で用いた単量体乳化物は、2-エチルヘキシルアクリレート(2-EHAと略記)69部、ブチルアクリレート(BAと略記す)30部、アクリル酸(AACと略記)1部の単量体混合物に、ポリオキシエチレンアルキルエーテル硫酸ナトリウム(花王株式会社製、商品名:ラテムルE-118B)4部とイオン交換水30部を混合し、乳化することで調製した。また、この単量体乳化物の滴下に並行して、5%濃度の過硫酸アンモニウム水溶液4部を滴下した。滴下終了後、80℃で4時間熟成し、その後、室温まで冷却した。最後に、アンモニア水で中和し、固形分を水で調整して、固形分60%、25℃における粘度が70mPa・s、pH8.0、比重カップでの比重が1.03である樹脂の水分散液の、アクリル系粘着剤エマルションA-1を得た。得られたエマルションA-1について、下記の方法で物性を測定し、その結果を表1中に、配合組成とともに記載した。
<粘度>
単一円筒回転式粘度計、いわゆるB型粘度計を用い、25℃で、回転数60rpmで測定した。
本発明では、エマルションのゲル分率を下記のようにして測定した。エマルションを、ポリラミシリコンセパレーター上に20g/m2/dryになるように塗工し、120℃の乾燥機で60秒間乾燥した。得られた皮膜試料1gをトルエン500gに24時間浸漬した。そして、24時間浸漬後、300メッシュステンレス金網でろ過し、ろ過後の残渣を熱風乾燥機で90℃、3時間乾燥させ、デシケーターに24時間放置後に残存皮膜の重量を測定し、浸漬前後の重量変化よりゲル分率を算出した。
本発明では、エマルションの平均粒子径を、レーザー回折式粒子径分布測定装置SALD-7100(株式会社島津製作所製)にて測定した。
本発明では、乾燥皮膜のテトラヒドロフラン可溶物の重量平均分子量を、ポリスチレンを標準物質とするGPC(Gel Permeation Chromatography)にて測定した。
合成例1における単量体混合物の構成成分及び配合量を、表1に記載のものに代えて、合成例1と同様の方法で、Tgがそれぞれ-45℃、-75℃のアクリル系粘着剤エマルションをそれぞれ調製した。これを、比較合成例の、アクリル系粘着剤エマルションA-2と、A-3とした。得られたエマルションA-2、A-3のそれぞれの物性についても、エマルションA-1の場合と同様に測定して、その結果を表1中に記載した。表1に示したように、A-2のTgは-45℃、A-3のTgは-75℃であり、いずれも本発明で規定する低Tgの範囲内のものではなかった。
温度計、撹拌機、滴下装置、還流冷却管及び窒素導入管を備えた反応装置に、イオン交換水28部を秤量し、窒素を封入して内温を80℃まで昇温させた。そして、その温度に保ちながら、10%濃度の過硫酸アンモニウム水溶液2部を添加し、直ちに、別に準備しておいた、下記のようにして調製した単量体乳化物を連続的に4時間滴下して乳化重合した。上記で用いた単量体乳化物は、2-エチルヘキシルアクリレート49部、メチルメタクリレート(MMAと略記)10部、スチレン(STと略記)40部、アクリル酸1部、タッキファイヤー(粘着付与樹脂)としてロジン系樹脂(荒川化学工業株式会社製、商品名:ペンセルD-125)50部の単量体混合物に、ポリオキシエチレンアルキルエーテル硫酸ナトリウム(花王株式会社製、商品名:ラテムルE-118B)4部とイオン交換水63部を混合し、乳化することで調製した。また、この単量体乳化物の滴下に並行して、5%濃度の過硫酸アンモニウム水溶液4部を滴下した。滴下終了後、80℃で4時間熟成し、その後室温まで冷却した。最後に、アンモニア水で中和し、固形分を水で調整して、固形分60%、25℃での粘度が100mPa・s、pH8.0、平均粒子径290nm、比重カップでの比重が1.05の樹脂の水分散液である、共重合体エマルションB-1を得た。また、モノマー組成から求めたB-1のTg値は、-8℃である。得られたエマルションB-1の物性についても、エマルションA-1と同様の方法で測定した。その結果を表2中に配合組成とともに記載した。また、図1に、B-1の平均粒子径を測定した際に得た粒度分布を示した。
合成例2における単量体構成成分及び配合量を、表2に記載のものに代えた以外は、合成例2と同様の方法で、共重合体エマルション(B-2)~(B-6)をそれぞれ作製した。得られたエマルション(B-2)~(B-6)のそれぞれの物性についても同様に測定して、その結果を表2中に配合組成とともに記載した。
合成例2における単量体構成成分及び配合量を、表2に記載のものに代えた以外は、合成例2と同様の方法で、共重合体エマルションB-7、B-8をそれぞれ作製した。得られたエマルションB-7、B-8についても同様に測定して、その結果を表2中に配合組成とともに記載した。表2に示したように、B-7のTgは-42℃、B-8のTgは40℃であり、いずれも本発明で規定する高Tgの範囲内のものではなかった。
合成例5の配合に加え、更に架橋剤として、トリメチロールプロパントリメタクリレート(共栄社化学株式会社製、商品名:ライトエステルTMP)を5部配合して、合成例2と同様の方法で、共重合体エマルションB-9を作製した。得られたエマルションB-9の物性を配合組成とともに表3に示した。表3に示したように、B-9の重量平均分子量は11万であり、本発明で規定する範囲内のものではなかった。
合成例5の配合において、ラテムルE-118Bを3倍量(12部)使用して、合成例2と同様の方法で、共重合体エマルションB-10を作製した。得られたエマルションB-10の物性を配合組成とともに表3に示した。表3に示したように、B-10の平均粒径は100nmであり、本発明で規定する範囲内のものではなかった。
合成例5の配合において、ラテムルE-118Bを0.5倍量(2部)使用して、合成例2と同様の方法で、共重合体エマルションB-11を作製した。得られたエマルションB-11の物性を配合組成とともに表3に示した。表3に示したように、B-11の平均粒径は2500nmであり、本発明で規定する範囲内のものではなかった。
合成例5の配合において、タッキファイヤー(粘着付与樹脂)であるペンセルD-125を使用せず、合成例2と同様の方法で、共重合体エマルションB-12を作製した。得られたエマルションB-12の物性を配合組成とともに表3に示した。表3に示したように、B-12の重量平均分子量は36万であり、本発明で規定する範囲内のものではなかった。
温度計、撹拌機、滴下装置、還流冷却管及び窒素導入管を備えた反応装置に、イオン交換水28部を秤量し、窒素を封入して内温を80℃まで昇温させ、その温度に保ちながら、10%濃度の過硫酸アンモニウム水溶液2部を添加し直ちに、別に準備した2-エチルヘキシルアクリレート55.5部、ブチルアクリレート28.5部、メチルメタクリレート15部、アクリル酸1部の単量体混合物に、タッキファイヤーとしてロジン系樹脂(荒川化学工業株式会社製、商品名:ペンセルD-125)15部、ポリオキシエチレンアルキルエーテル硫酸ナトリウム(花王株式会社製、商品名:ラテムルE-118B)4部とイオン交換水40部を混合し乳化した単量体乳化物を、連続的に4時間滴下して乳化重合した。並行して5%濃度の過硫酸アンモニウム水溶液4部を滴下した。滴下終了後、80℃で4時間熟成し、その後室温まで冷却した。アンモニア水で中和し、固形分を水で調整して、固形分60%、25℃における粘度が500mPa・s、pH8.0なる水分散液を得た。これを共重合体エマルションAB-1とし、その物性を配合組成とともに表3中に示した。AB-1は、低Tgの単量体と高Tgの単量体に、タッキファイヤーを加えて乳化重合したものであり、本発明で規定する構成とは全く異なる。
上記した合成例1と比較合成例1、2で得たアクリル系粘着剤エマルション(A-1)~(A-3)と、上記した合成例2~7及び比較合成例3~8で得た共重合体エマルション(B-1)~(B-12)とを用い、表4-1、表4-2に記載した組み合わせと割合で配合し、増粘剤で粘度を500mPa・s程度に調整することにより、本発明の実施例と比較例のエマルション型粘着剤組成物をそれぞれに得た。また、上記した比較合成例9で得た共重合体エマルション(AB-1)を用いたものを比較例7のエマルション型粘着剤組成物とした。なお、表4-2中のタッキファイヤーエマルションには、荒川化学工業株式会社製のスーパーエステルE-730-55(商品名、粘度40mPa・s、平均粒子径500nm、比重1.05)を使用した。上記のようにして調製した実施例1のアクリル系粘着剤エマルションについて、下記の方法で測定したレオメーターでのずり速度104s-1時の粘度は、100mPa・sであった。
レオメーターによる粘度測定は下記のようにして行った。粘弾性測定装置Physica MCR301(Anton Paar社製)にてコーンプレートを使用して、25℃の条件で、ずり速度104s-1までの粘度を測定した。
比較例8、9の粘着剤組成物は、比較合成例1、2で作製したアクリル系粘着剤エマルションA-2と、A-3とをそれぞれに用い、併用する共重合体エマルション(B)として、合成例5で作製した本発明で規定する共重合体エマルション(B-4)を用い、実施例4と同様にして粘着剤組成物を作製したものである。
比較例10、11の粘着剤組成物は、合成例1で得た本発明で規定するアクリル系粘着剤エマルション(A-1)と、合成例5で作製した本発明で規定する共重合体エマルション(B-4)を用い、両者の使用比率を本発明で規定する範囲外としたものである。
上記した表4-1に示した配合を有する実施例の各エマルション型粘着剤組成物と、上記した表4-2に示した配合を有する比較例の各エマルション型粘着剤組成物のそれぞれについて、下記の方法及び基準で性能を評価した。具体的には、粘着力及びループタックを測定し、性能を評価するとともに、液の安定性を下記の基準で評価した。そして、表5に、得られた結果をまとめて示した。先の方法で測定した粘度についても、表5中にまとめて示した。
(試験用の試料の作製)
実施例及び比較例の各エマルション型粘着剤組成物を、ポリラミシリコンセパレーター上に20g/m2/dryになるように塗工し、120℃の乾燥機で60秒間乾燥後、粘着層上に上質紙(64g/m2)を貼り合わせ、23℃、50%RH雰囲気中に16時間以上放置して、粘着シートを作製し、これを試験試料とした。また、該試験試料は、同じ条件で複数作製し、下記の試験に用いた。
上記で得た試験試料を、23℃、50%RH雰囲気中で、ステンレス板に圧着した直後の180°はくり強度を、JIS Z0237粘着テープ・粘着シート試験方法に準じ、テンシロンにて測定した。そして、粘着力については、測定値が15N/25mm以上のものを、高粘着力のものであると評価した。表5に、得られた測定値を示した。
上記で得た試験試料を、23℃、50%RH雰囲気中で、ループ状にして、水平にしたステンレス板に貼り付け、300mm/minの速度で引き剥がした時の強度をテンシロンにて測定した。そして、タックについては、13N/25mm以上のものを高タックのものであると評価した。表5に、得られた測定値を示した。
実施例及び比較例の各エマルション型粘着剤組成物について、製造時の凝集物の有無や、放置後(3ヶ月)の液の分離状態を目視で確認し、評価した。表5中の「○」は、製造時に凝集物がなく、放置後に液の分離がなかったことを意味する。一方、「凝集」は製造時に凝集物があったことを意味し、「分離」は放置後の液が分離したことを意味する。表5に、評価結果を示した。
Claims (5)
- 主成分として低Tgのアクリル系粘着剤エマルション(A)を51~90質量%、副成分として高Tgの共重合体エマルション(B)を10~49質量%の範囲内で含む、少なくともこれら2種類のエマルションの混合物を含有してなるエマルション型粘着剤組成物であって、
その固形分が50%以上で、25℃での粘度が1000mPa・s以下であり、
前記低Tgのアクリル系粘着剤エマルション(A)は、そのガラス転移温度(Tg)が-70℃~-50℃であり、
前記高Tgの共重合体エマルション(B)は、少なくとも(メタ)アクリル酸アルキルエステル系単量体を含む単量体混合物100質量部に、20~200質量部の粘着付与樹脂を存在させて乳化重合した共重合体のエマルションであり、該共重合体のガラス転移温度(Tg)が-30℃~30℃で、その重量平均分子量が5000~70000で、且つ、その平均粒子径が200~2000nmであることを特徴とするエマルション型粘着剤組成物。 - 前記粘着付与樹脂の量が、前記(メタ)アクリル酸アルキルエステル系単量体を含む単量体混合物100質量部に対して、40~120質量部の範囲内であり、前記共重合体の重量平均分子量が5000~60000である請求項1に記載のエマルション型粘着剤組成物。
- 前記低Tgのアクリル系粘着剤エマルション(A)を60~80質量%、副成分として高Tgの共重合体エマルション(B)を20~40質量%の範囲内で含む請求項1又は2に記載のエマルション型粘着剤組成物。
- 前記低Tgのアクリル系粘着剤エマルション(A)の25℃での粘度が、50~700mPa・sの範囲内であり、且つ、前記高Tgの共重合体エマルション(B)の25℃での粘度が、50~1000mPa・sの範囲内である請求項1~3のいずれか1項に記載のエマルション型粘着剤組成物。
- 前記粘着付与樹脂の軟化点(℃)が、70℃~170℃である請求項1~4のいずれか1項に記載のエマルション型粘着剤組成物。
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Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5958069A (ja) * | 1982-09-27 | 1984-04-03 | Hoechst Gosei Kk | 強接着性エマルジヨン型粘着剤 |
US20030077443A1 (en) * | 2001-07-06 | 2003-04-24 | Di Stefano Frank Vito | Blends of high Tg polymer emulsions and pressure sensitive adhesive polymer emulsions useful as pressure sensitive adhesives |
JP2005239875A (ja) * | 2004-02-26 | 2005-09-08 | Soken Chem & Eng Co Ltd | 粘着性向上剤、それを含有する(メタ)アクリル系粘着剤組成物及び粘着シート |
JP2006509890A (ja) * | 2002-12-13 | 2006-03-23 | イーストマン ケミカル カンパニー | 水性組成物の製造方法 |
JP2012126889A (ja) * | 2010-11-25 | 2012-07-05 | Nitto Denko Corp | 光学フィルム用粘着剤層、粘着剤層付光学フィルム、画像表示装置および光学フィルムの剥離方法 |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH07107150B2 (ja) * | 1987-03-27 | 1995-11-15 | 日本合成ゴム株式会社 | エマルジヨン型感圧接着剤 |
US20030143409A1 (en) * | 2001-07-06 | 2003-07-31 | Di Stefano Frank Vito | Blends of high Tg polymer emulsions and pressure sensitive adhesive polymer emulsions useful as pressure sensitive adhesives |
JP3942150B2 (ja) * | 2001-09-26 | 2007-07-11 | 日本合成化学工業株式会社 | エマルジョン型粘着剤組成物 |
JP4795766B2 (ja) * | 2004-09-30 | 2011-10-19 | 株式会社日本触媒 | エマルション型粘着剤組成物 |
-
2015
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Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5958069A (ja) * | 1982-09-27 | 1984-04-03 | Hoechst Gosei Kk | 強接着性エマルジヨン型粘着剤 |
US20030077443A1 (en) * | 2001-07-06 | 2003-04-24 | Di Stefano Frank Vito | Blends of high Tg polymer emulsions and pressure sensitive adhesive polymer emulsions useful as pressure sensitive adhesives |
JP2006509890A (ja) * | 2002-12-13 | 2006-03-23 | イーストマン ケミカル カンパニー | 水性組成物の製造方法 |
JP2005239875A (ja) * | 2004-02-26 | 2005-09-08 | Soken Chem & Eng Co Ltd | 粘着性向上剤、それを含有する(メタ)アクリル系粘着剤組成物及び粘着シート |
JP2012126889A (ja) * | 2010-11-25 | 2012-07-05 | Nitto Denko Corp | 光学フィルム用粘着剤層、粘着剤層付光学フィルム、画像表示装置および光学フィルムの剥離方法 |
Non-Patent Citations (1)
Title |
---|
See also references of EP3246372A4 * |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2017186387A (ja) * | 2016-03-31 | 2017-10-12 | 株式会社日本触媒 | 水分散型アクリル系粘着剤組成物 |
CN112689505A (zh) * | 2018-09-26 | 2021-04-20 | 日绊株式会社 | 含水贴剂 |
JP2020084121A (ja) * | 2018-11-30 | 2020-06-04 | 東洋インキScホールディングス株式会社 | 水性感圧式接着剤、感圧式接着シート、および水性感圧式接着剤の製造方法 |
JP7468110B2 (ja) | 2020-04-17 | 2024-04-16 | artience株式会社 | 水性感圧式接着剤、感圧式接着シート、および水性感圧式接着剤の製造方法 |
Also Published As
Publication number | Publication date |
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EP3246372B1 (en) | 2020-01-08 |
EP3246372A1 (en) | 2017-11-22 |
CN106459707B (zh) | 2018-02-16 |
CN106459707A (zh) | 2017-02-22 |
EP3246372A4 (en) | 2018-08-22 |
JP6183821B2 (ja) | 2017-08-23 |
JPWO2016114010A1 (ja) | 2017-05-18 |
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