Patent Application
20130034730
The present invention relates to removable water-dispersible acrylic pressure-sensitive adhesive compositions. Specifically, the present invention relates to removable water-dispersible acrylic pressure-sensitive adhesive compositions capable of forming pressure-sensitive adhesive layers which less suffer from appearance defects such as dimples, have good appearances, and are satisfactorily resistant to increase in adhesive strength with time. The present invention also relates to pressure-sensitive adhesive sheets including pressure-sensitive adhesive layers formed from the pressure-sensitive adhesive compositions.
Surface-protecting films are applied to surfaces of optical members (optical elements; optical materials) typically for preventing surface flaws and stains, improving cutting workability, and reducing cracking in production and working processes of the optical members, in which the optical members are typified by polarizing plates, retardation films, and anti-reflective films (see Patent Literature (PTL) 1 and PTL 2). Such surface-protecting films generally employ removable pressure-sensitive adhesive sheets each including a plastic film substrate and, on a surface thereof, a removable pressure-sensitive adhesive layer.
Solvent-borne acrylic pressure-sensitive adhesives have been used as pressure-sensitive adhesives for the surface-protecting films (see PTL 1 and PTL 2). Attempts, however, have been made to switch the solvent-borne acrylic pressure-sensitive adhesives to water-dispersive acrylic pressure-sensitive adhesives (see PTL 3, PTL 4, and PTL 5), because the solvent-borne acrylic pressure-sensitive adhesives contain organic solvents and may thereby adversely affect working environmental conditions upon application (coating) of the adhesives.
The surface-protecting films should exhibit sufficient adhesiveness during affixation to optical members. In addition, they should exhibit excellent peelability (removability) because they will be peeled off (removed) after being used typically in production processes of optical members. For having excellent removability, surface-protecting films should have a small peel strength (light releasability) and, in addition, have such a property as not to increase in adhesive strength (peel strength) with time after the affixation to an adherend such as an optical member. This property is also referred to as “resistance to increase in adhesive strength.”
The use of a water-insoluble crosslinking agent in a pressure-sensitive adhesive (or in a pressure-sensitive adhesive composition) is effective in obtaining the properties such as light releasability and resistance to increase in adhesive strength. Pressure-sensitive adhesive compositions using a water-insoluble crosslinking agent are exemplified by removable water-dispersible acrylic pressure-sensitive adhesive compositions containing an oil-soluble crosslinking agent (see PTL 6 and PTL 7).
However, the aforementioned pressure-sensitive adhesive compositions and other water-dispersible acrylic pressure-sensitive adhesive compositions using a water-insoluble crosslinking agent may include the water-insoluble crosslinking agent being insufficiently dispersed and remaining as large particles, and the large particles may often cause “dimples” and other appearance defects on the surface of a pressure-sensitive adhesive layer upon the formation thereof. Particularly when the water-insoluble crosslinking agent is used to form a pressure-sensitive adhesive layer of a surface-protecting film, the appearance defects may disadvantageously impede the inspection of the adherend with the surface-protecting film affixed thereto.
Under these present circumstances, no removable water-dispersible acrylic pressure-sensitive adhesive has been obtained, which is capable of forming a pressure-sensitive adhesive layer having excellent adhesiveness and removability (particularly, superior resistance to increase in adhesive strength), less suffering from appearance defects such as “dimples,” and having a good appearance.
Such a water-dispersible acrylic pressure-sensitive adhesive composition contains a surfactant component for stable dispersibility in water, but the presence of the surfactant component causes the pressure-sensitive adhesive composition to be susceptible to foaming. In particular, the pressure-sensitive adhesive composition, when stirred in a stirring process, is liable to include air as bubbles, and the included bubbles are stabilized by the surfactant and become resistant to escaping out. The bubbles may remain in a pressure-sensitive adhesive layer formed from the pressure-sensitive adhesive composition or may form, for example, “dimples” in the surface of the pressure-sensitive adhesive layer, thus disadvantageously forming appearance defects. For example, when the pressure-sensitive adhesive layer is used as a pressure-sensitive adhesive layer of a surface-protecting film, the appearance defects may impede the inspection of the adherend with the surface-protecting film affixed thereto.
Particularly when used in (used to form) a surface-protecting film (particularly a surface-protecting film for an optical member), the pressure-sensitive adhesive composition is strongly desired to give a surface-protecting film without defects derived from bubbles. Specifically, if the surface-protecting film used in such applications has a pressure-sensitive adhesive layer with appearance defects, the appearance defects may impede quality inspection and/or quality control. This is because bubbles remained in the pressure-sensitive adhesive layer and “dimples” present in the surface of the pressure-sensitive adhesive layer are hardly distinguishable as defects of the surface-protecting film itself or as defects of the member (adherend such as optical member) to which the film is affixed.
As a possible solution to improvements (reduction) of the defects derived from bubbles, defoaming agents are added, of which silicone defoaming agents and hydrophobic-silica-containing defoaming agents are expected for their satisfactory defoaming properties (see PTL 8 and 9).
However, the silicone defoaming agents are less uniformly dispersible in a pressure-sensitive adhesive composition, thereby locally form a highly hydrophobic portion, and this causes crawling upon the application of the pressure-sensitive adhesive composition. The silicone defoaming agents have poor miscibility (compatibility) with the acrylic emulsion polymer, thereby bleed out on the surface of the pressure-sensitive adhesive layer after its formation, and cause contamination (staining) to the adherend. Particularly when a resulting pressure-sensitive adhesive sheet including the pressure-sensitive adhesive layer is used in a surface-protecting film for an optical member, the contaminant may significantly disadvantageously affect the optical properties of the adherend optical member.
In contrast, the defoaming agents containing hydrophobic silica are satisfactorily uniformly dispersible in a pressure-sensitive adhesive composition, but the hydrophobic silica contained therein forms secondary aggregates to cause defects derived from or occurring from the silica particles. Independently, the pressure-sensitive adhesive composition, when used for the formation of surface-protecting films for optical members, is generally filtrated typically through a filter to remove foreign matter from the composition, because such foreign matter, if present, will form optical defects. In the filtration, the filter may be clogged with the silica particles, and this disadvantageously reduces production efficiency.
In addition, pressure-sensitive adhesives and pressure-sensitive adhesive layers for use in surface-protecting films (particularly, in surface-protecting films for optical members) are strongly desired to less stain the adherend (e.g., an optical member). This is because staining (contamination) of the surface of the adherend may adversely affect optical properties of the optical member. The staining is due typically to remaining of the pressure-sensitive adhesive on the surface of the adherend (so-called “adhesive residue”) and due to migration of components contained in the pressure-sensitive adhesive layer into the adherend surface upon removal of the pressure-sensitive adhesive sheet.
An object of the present invention is to provide a water-dispersible acrylic pressure-sensitive adhesive composition capable of forming a removable pressure-sensitive adhesive layer which is satisfactorily resistant to increase in adhesive strength, has a good appearance (with less appearance defects such as dimples), and less causes staining. Another object of the present invention is to provide a pressure-sensitive adhesive sheet having a pressure-sensitive adhesive layer formed from the pressure-sensitive adhesive composition.
After intensive investigations to achieve the objects, the present inventors have found a water-dispersible acrylic pressure-sensitive adhesive composition containing an acrylic emulsion polymer formed from constitutive monomers in a specific formulation, a water-insoluble crosslinking agent, a specific acetylenic diol compound, and a specific polyether defoaming agent as components; and have found that the water-dispersible acrylic pressure-sensitive adhesive composition is capable of forming a pressure-sensitive adhesive layer which is satisfactorily resistant to increase in adhesive strength, has a good appearance, and less causes staining. The present invention has been made based on these findings.
Specifically, the present invention provides a removable water-dispersible acrylic pressure-sensitive adhesive composition including an acrylic emulsion polymer (A); a water-insoluble crosslinking agent (B); an acetylenic diol compound (C); and a polyether defoaming agent (D), in which the acrylic emulsion polymer (A) is formed from constitutive monomers essentially containing a (meth)acrylic alkyl ester in a content of from 70 to 99.5 percent by weight and a carboxyl-containing unsaturated monomer in a content of from 0.5 to 10 percent by weight, each based on the total amount of the constitutive monomers, the polyether defoaming agent (D) is at least one compound selected from the group consisting of a compound represented by following Formula (I), a compound represented by following Formula (II), and a compound represented by following Formula (III), the acetylenic diol compound (C) has a hydrophile-lypophile balance (HLB) of less than 13, and the polyether defoaming agent (D) has a propylene oxide in a content of from 70 to 100 percent by weight and a number-average molecular weight of from 1200 to 4000:
RaO—(PO)n1(EO)m1—CO—Rb (I)
wherein PO represents oxypropylene group; EO represents oxyethylene group; Ra represents an alkyl or alkenyl group having 8 to 22 carbon atoms, or an alkylcarbonyl or alkenylcarbonyl group having 8 to 21 carbon atoms; Rb represents an alkyl or alkenyl group having 8 to 21 carbon atoms; m1 denotes an integer of from 0 to 15; and n1 denotes an integer of 1 or more, where EO and PO are added in a random manner or block manner,
RcO—(PO)n2(EO)m2—H (II)
wherein PO represents oxypropylene group; EO represents oxyethylene group; Ro represents nonylphenyl group, octylphenyl group, or an alkyl or alkenyl group having 8 to 22 carbon atoms; m2 denotes an integer of from 0 to 20; and n2 denotes an integer of 1 or more, where EO and PO are added in a random manner or block manner, and
HO—(PO)n3(EO)m3—H (III)
wherein PO represents oxypropylene group; EO represents oxyethylene group; m3 denotes an integer of from 0 to 40; and n3 denotes an integer of 1 or more, where EO and PO are added in a random manner or block manner.
The acrylic emulsion polymer (A) in the removable water-dispersible acrylic pressure-sensitive adhesive composition may be a polymer polymerized with a reactive emulsifier containing a radically polymerizable functional group in the molecule.
In the removable water-dispersible acrylic pressure-sensitive adhesive composition, it is preferred that the water-insoluble crosslinking agent (B) has carboxyl-reactive functional groups being reactive with carboxyl group, and the carboxyl-reactive functional groups are present in an amount of from 0.3 to 1.3 moles per mole of carboxyl group of the carboxyl-containing unsaturated monomer.
The present invention further provides a pressure-sensitive adhesive sheet including a substrate and, on at least one side thereof, a pressure-sensitive adhesive layer formed from the removable water-dispersible acrylic pressure-sensitive adhesive composition.
The pressure-sensitive adhesive layer in the pressure-sensitive adhesive sheet may have a solvent-insoluble content of 90 percent by weight or more and an elongation at break of 200% or less.
The pressure-sensitive adhesive sheet may serve as a surface-protecting film for an optical member.
Pressure-sensitive adhesive compositions according to embodiments of the present invention are dispersible in water and have the above configuration. Pressure-sensitive adhesive layers formed from the pressure-sensitive adhesive compositions, and pressure-sensitive adhesive sheet having the pressure-sensitive adhesive layers therefore have excellent removability, satisfactory adhesiveness, and good appearances, cause (leave) substantially no stain on the surface of an adherend after removal, and thus less cause staining. They are also resistant to increase in adhesive strength to the adherend with time. For these reasons, they are useful for the surface protection of optical films.
A removable water-dispersible acrylic pressure-sensitive adhesive composition (hereinafter also simply referred to as “pressure-sensitive adhesive composition”) according to an embodiment of the present invention contains an acrylic emulsion polymer (A), a water-insoluble crosslinking agent (B), an acetylenic diol compound (C), and a polyether defoaming agent (D) as essential components.
The acrylic emulsion polymer (A) for use in the pressure-sensitive adhesive composition according to the present invention is a polymer formed from a (meth)acrylic alkyl ester and a carboxyl-containing unsaturated monomer as essential constitutive monomers (constitutive monomer components). Specifically, the acrylic emulsion polymer (A) is a polymer formed from a monomer mixture containing a (meth)acrylic alkyl ester and a carboxyl-containing unsaturated monomer as essential components. Each of different acrylic emulsion polymers (A) may be used alone or in combination. As used herein the term “(meth)acrylic” refers to “acrylic” and/or “methacrylic.”
The (meth)acrylic alkyl ester is used as a principal monomer component constituting the acrylic emulsion polymer (A) and mainly performs the function of developing adhesiveness, peelability, and other basic properties as a pressure-sensitive adhesive (or as a pressure-sensitive adhesive layer). Of (meth)acrylic alkyl esters, acrylic alkyl esters may effectively impart flexibility to the polymer constituting the pressure-sensitive adhesive layer and may help the pressure-sensitive adhesive layer to develop adhesion and tackiness; and methacrylic alkyl esters may impart hardness (rigidity) to the polymer constituting the pressure-sensitive adhesive layer and may help the pressure-sensitive adhesive layer to have controlled removability. The (meth)acrylic alkyl ester is exemplified by, but is not limited to, (meth)acrylic alkyl esters whose alkyl moiety being a linear, branched chain, or cyclic alkyl group having 1 to 16 (more preferably 2 to 10, and furthermore preferably 4 to 8) carbon atoms.
Of acrylic alkyl esters, preferred are acrylic alkyl esters whose alkyl moiety having 2 to 14 carbon atoms (more preferably 4 to 8 carbon atoms), which are typified by acrylic alkyl esters whose alkyl moiety being a linear or branched chain alkyl group, such as n-butyl acrylate, isobutyl acrylate, s-butyl acrylate, isoamyl acrylate, hexyl acrylate, heptyl acrylate, octyl acrylate, 2-ethylhexyl acrylate, isooctyl acrylate, nonyl acrylate, and isononyl acrylate. Among them, 2-ethylhexyl acrylate and n-butyl acrylate are more preferred.
Of methacrylic alkyl esters, preferred are methacrylic alkyl esters whose alkyl moiety having 2 to 16 carbon atoms (more preferably 2 to 8 carbon atoms), which are typified by methacrylic alkyl esters whose alkyl moiety being a linear or branched chain alkyl group, such as ethyl methacrylate, propyl methacrylate, isopropyl methacrylate, n-butyl methacrylate, isobutyl methacrylate, s-butyl methacrylate, and t-butyl methacrylate; and alicyclic methacrylic alkyl esters such as cyclohexyl methacrylate, bornyl methacrylate, and isobornyl methacrylate. Among them, n-butyl methacrylate is particularly preferred.
Methyl methacrylate and/or isobornyl acrylate may be used as the (meth)acrylic alkyl ester to help the pressure-sensitive adhesive layer to have a better appearance as mentioned later.
The (meth)acrylic alkyl ester can be suitably chosen according typically to the intended tackiness, and each of different (meth)acrylic alkyl esters may be used alone or in combination.
The (meth)acrylic alkyl ester(s) is contained in a content of from 70 to 99.5 percent by weight, more preferably from 85 to 99 percent by weight, and furthermore preferably from 91 to 98 percent by weight, based on the total amount (100 percent by weight) of constitutive monomers (total constitutive monomers) constituting the acrylic emulsion polymer (A). The (meth)acrylic alkyl ester(s), if present in a content of more than 99.5 percent by weight, causes an excessively small relative content of the carboxyl-containing unsaturated monomer(s), and this may cause a pressure-sensitive adhesive layer formed from the pressure-sensitive adhesive composition to have insufficient anchoring capability, to cause stains, and to have insufficient emulsion stability. The (meth)acrylic alkyl ester(s), if present in a content of less than 70 percent by weight, may cause the pressure-sensitive adhesive layer to have insufficient adhesiveness and removability. Though not critical, the ratio of the content of acrylic alkyl ester(s) to the content of methacrylic alkyl ester(s) in the (meth)acrylic alkyl esters [(content of acrylic alkyl ester(s)):(content of methacrylic alkyl ester(s))] is preferably from 100:0 to 30:70 (by weight), and more preferably from 100:0 to 50:50.
The carboxyl-containing unsaturated monomer exhibit the function of forming a protective layer on surfaces of emulsion particles including the acrylic emulsion polymer (A) to prevent the shear fracture of the emulsion particles. This function is further improved by neutralizing the carboxyl group with a base. The stability of the particles against shear fracture is more generally referred to as mechanical stability. The carboxyl-containing unsaturated monomer may be used in combination with one or more multifunctional compounds (e.g., multifunctional epoxy compounds) being reactive with carboxyl group. This may allow the carboxyl-containing unsaturated monomer to act as crosslinking points during the formation of the pressure-sensitive adhesive layer through removal of water. In addition, the carboxyl-containing unsaturated monomer may increase adhesion (anchoring capacity) of the pressure-sensitive adhesive layer to the substrate through the multifunctional compounds. Exemplary carboxyl-containing unsaturated monomers include (meth)acrylic acid (acrylic acid and methacrylic acid), itaconic acid, maleic acid, fumaric acid, crotonic acid, carboxyethyl acrylate, and carboxypentyl acrylate. As used herein the term “carboxyl-containing unsaturated monomer” also includes unsaturated monomers containing an acid anhydride group, such as maleic anhydride and itaconic anhydride. Among them, acrylic acid is preferred because of easily having a high relative concentration in the surface of the emulsion particles to form a denser protective layer. Each of different carboxyl-containing unsaturated monomers may be used alone or in combination.
The carboxyl-containing unsaturated monomer(s) is contained in a content of from 0.5 to 10 percent by weight, preferably from 1 to 5 percent by weight, and more preferably from 2 to 4 percent by weight, based on the total amount (100 percent by weight) of constitutive monomers (total constitutive monomers) constituting the acrylic emulsion polymer (A). The carboxyl-containing unsaturated monomer(s), if present in a content of more than 10 percent by weight, may undergo polymerization in water to cause thickening (increase in viscosity), because such carboxyl-containing unsaturated monomers (e.g., acrylic acid) are generally soluble in water. In addition, such an excessively large amount of the carboxyl-containing unsaturated monomer(s) may cause the pressure-sensitive adhesive layer to have, after its formation, an increasing interaction with a functional group on the surface of the adherend (e.g., polarizing plate) to thereby have an increasing adhesive strength with time, and this may impede the removal of the pressure-sensitive adhesive layer from the adherend. The carboxyl-containing unsaturated monomer(s), if present in a content of less than 0.5 percent by weight, may cause the emulsion particles to have insufficient mechanical stability and may cause insufficient adhesion (anchoring capability) between the pressure-sensitive adhesive layer and the substrate, thus causing adhesive residue.
Monomer components (constitutive monomers) constituting the acrylic emulsion polymer (A) may further include one or more additional monomer components for imparting a specific function, in addition to the (meth)acrylic alkyl esters and the carboxyl-containing unsaturated monomers. Exemplary additional monomer components are as follows. For higher cohesive force, the monomer components may contain (employ) any of amido-containing monomers such as (meth)acrylamide, N,N-diethyl(meth)acrylamide, and N-isopropyl(meth)acrylamide; and amino-containing monomers such as N,N-dimethylaminoethyl(meth)acrylate and N,N-dimethylaminopropyl(meth)acrylate, in an amount per each category of from about 0.1 to about 15 percent by weight. For the control of refractive index and/or for satisfactory reworkability, the monomer components may contain (employ) any of (meth)acrylic aryl esters such as phenyl(meth)acrylate; vinyl esters such as vinyl acetate and vinyl propionate; and styrenic monomers such as styrene, in an amount per each category of 15 percent by weight or less. For improving crosslinking in the emulsion particles and for higher cohesive force, the monomer components may contain (employ) any of epoxy-containing monomers such as glycidyl(meth)acrylate and allyl glycidyl ether; and multifunctional monomers such as trimethylolpropane tri(meth)acrylate and divinylbenzene, in an amount per each category of less than 5 percent by weight. For forming hydrazide crosslinks with a combination use of a hydrazide crosslinking agent to further less cause staining, the monomer components may contain (employ) any of keto-containing unsaturated monomers such as diacetoneacrylamide (DAAM), allyl acetoacetate, and 2-(acetoacetoxy)ethyl(meth)acrylate in an amount of less than 10 percent by weight, and preferably from 0.5 to 5 percent by weight.
A hydroxyl-containing unsaturated monomer may be used as the additional monomer component. The hydroxyl-containing unsaturated monomer is typified by 2-hydroxyethyl(meth)acrylate, 2-hydroxypropyl(meth)acrylate, 4-hydroxybutyl(meth)acrylate, 6-hydroxyhexyl(meth)acrylate, 8-hydroxyoctyl(meth)acrylate, 10-hydroxydecyl(meth)acrylate, 12-hydroxylauryl(meth)acrylate, (4-hydroxymethylcyclohexyl)methyl acrylate, N-methylol(meth)acrylamide, vinyl alcohol, allyl alcohol, 2-hydroxyethyl vinyl ether, 4-hydroxybutyl vinyl ether, and diethylene glycol monovinyl ether. The amount of the hydroxyl-containing unsaturated monomer to be added (used) is preferably minimized for further less causing whitening as stains. Specifically, the amount of the hydroxyl-containing unsaturated monomer is preferably less than 1 percent by weight, more preferably less than 0.1 percent by weight, and furthermore preferably substantially zero (substantially no hydroxyl-containing unsaturated monomer is contained) (e.g., the content is less than 0.05 percent by weight). However, such a hydroxyl-containing unsaturated monomer may be added (used) in an amount of from about 0.01 to about 10 percent by weight for the purpose of introducing crosslinking points in crosslinking between hydroxyl group and isocyanate group or in metal crosslinking.
The amounts (contents) of the additional monomer components to be added (used) are indicated as contents based on the total amount (100 percent by weight) of constitutive monomers (total constitutive monomers) constituting the acrylic emulsion polymer (A).
The monomer components (constitutive monomers) constituting the acrylic emulsion polymer (A) preferably contain (employ) at least one monomer selected from the group consisting of methyl methacrylate, isobornyl acrylate, N,N-diethylacrylamide, and vinyl acetate, of which methyl methacrylate is more preferred, particularly for a better appearance of the pressure-sensitive adhesive sheet (pressure-sensitive adhesive layer) formed from the pressure-sensitive adhesive composition according to the present invention. The monomer(s) (monomer(s) selected from the group consisting of methyl methacrylate, isobornyl acrylate, N,N-diethylacrylamide, and vinyl acetate) may be contained in a content of preferably from 0.5 to 15 percent by weight, more preferably from 1 to 10 percent by weight, and furthermore preferably from 2 to 5 percent by weight, based on the total amount (100 percent by weight) of constitutive monomers (total constitutive monomers) constituting the acrylic emulsion polymer (A). The monomer(s), if present in a content of less than 0.5 percent by weight, may not effectively contribute to the better appearance; and the monomer(s), if present in a content of more than 15 percent by weight, may cause the polymer constituting the pressure-sensitive adhesive layer to be excessively rigid, thus causing insufficient adhesion. When two or more monomers selected from the group consisting of methyl methacrylate, isobornyl acrylate, N,N-diethylacrylamide, and vinyl acetate are contained in the constitutive monomers constituting the acrylic emulsion polymer (A), the total amount (total content) of methyl methacrylate, isobornyl acrylate, N,N-diethylacrylamide, and vinyl acetate may fall within the above-specified range.
The acrylic emulsion polymer (A) for use in the present invention may be obtained by emulsion polymerization of the constitutive monomers (monomer mixture) with an emulsifier and a polymerization initiator. The emulsion polymerization may further employ a chain-transfer agent for controlling the molecular weight of the acrylic emulsion polymer (A).
The emulsifier for use in the emulsion polymerization to form the acrylic emulsion polymer (A) is preferably a reactive emulsifier having a radically polymerizable functional group introduced into the molecule (reactive emulsifier containing a radically polymerizable functional group). Each of different emulsifiers may be used alone or in combination.
The reactive emulsifier containing a radically polymerizable functional group (hereinafter also simply referred to as “reactive emulsifier”) is an emulsifier containing at least one radically polymerizable functional group in the molecule (per molecule). The reactive emulsifier is typified by, but is not limited to, reactive emulsifiers having one or more radically polymerizable functional groups such as vinyl groups, propenyl groups, isopropenyl groups, vinyl ether groups (vinyloxy groups), and allyl ether groups (allyloxy groups). Each of different reactive emulsifiers may be used alone or in combination. The reactive emulsifier, when used, is taken into the polymer, and this may advantageously reduce stains derived from the emulsifier.
The reactive emulsifier is typified by reactive emulsifiers having a structure (or corresponding to the structure) of a nonionic-anionic emulsifier (anionic emulsifier having a nonionic hydrophilic group), except with an introduced radically polymerizable functional group (radically reactive group) such as propenyl group or allyl ether group. Exemplary nonionic-anionic emulsifiers include sodium polyoxyethylene alkyl ether sulfates, ammonium polyoxyethylene alkyl phenyl ether sulfates, sodium polyoxyethylene alkyl phenyl ether sulfates, and sodium polyoxyethylene alkyl sulfosuccinates. Hereinafter a reactive emulsifier having a structure corresponding to an anionic emulsifier, except with a radically polymerizable functional group being introduced, is referred to as an “anionic reactive emulsifier”; and a reactive emulsifier having a structure corresponding to a nonionic-anionic emulsifier, except with a radically polymerizable functional group being introduced, is referred to as a “nonionic-anionic reactive emulsifier.”
Among them, anionic reactive emulsifiers are preferred, of which nonionic-anionic reactive emulsifiers are more preferred, because these emulsifiers will be taken into the polymer to less cause staining. Such an anionic reactive emulsifier, as having a catalytic activity, can also help the water-insoluble crosslinking agent (B) to exhibit better reactivity, particularly when the crosslinking agent is a multifunctional epoxy crosslinking agent having epoxy groups. If no anionic reactive emulsifier is used, the crosslinking reaction may not complete even through aging, and the resulting pressure-sensitive adhesive layer may disadvantageously have an adhesive strength varying with time. The pressure-sensitive adhesive layer in this case may also contain unreacted carboxyl groups to suffer from increase in adhesive strength to the adherend with time. The anionic reactive emulsifiers are also preferred because they are taken into the polymer, thereby do not precipitate to the surface of the adherend, and cannot cause whitening as stains, unlike quaternary ammonium compounds (e.g., see JP-A No. 2007-31585) which are generally used as catalysts for epoxy crosslinking agents and which precipitate to the surface of the adherend.
The reactive emulsifiers may also be available as commercial products such as those available under the trade name “ADEKA REASOAP SE-10N” (from ADEKA CORPORATION), the trade name “ADEKA REASOAP SE-20N” (from ADEKA CORPORATION), the trade name “ADEKA REASOAP SR-10” (from ADEKA CORPORATION), the trade name “ADEKA REASOAP SR-20” (from ADEKA CORPORATION), the trade name “AQUALON HS-10” (from Dai-ichi Kogyo Seiyaku Co., Ltd.), the trade name “AQUALON HS-05” (from Dai-ichi Kogyo Seiyaku Co., Ltd.), and the trade name “LATEMUL PD-104” (from Kao Corporation).
The emulsifier for use herein is preferably one having a SO42− ion concentration of 100 μg/g or less, from which impurity ions have been removed, because such impurity ions may adversely affect the composition. Of the anionic emulsifiers, ammonium salt emulsifiers are desirably used. The removal of impurities from the emulsifier may be performed by a suitable process such as a process of removing impurities using an ion-exchange resin, a process of separating impurities using a membrane, or a process of precipitating impurities from an alcohol and removing the precipitates by filtration.
The reactive emulsifier may be incorporated (used) in an amount of preferably from 0.1 to 10 parts by weight, more preferably from 0.5 to 6 parts by weight, furthermore preferably from 1 to 4.5 parts by weight, and most preferably from 1 to 3 parts by weight, per 100 parts by weight of the total amount of constitutive monomers (total constitutive monomers) constituting the acrylic emulsion polymer (A). The reactive emulsifier, if present in an amount of more than 10 parts by weight, may cause the pressure-sensitive adhesive (pressure-sensitive adhesive layer) to have insufficient cohesive force, resulting in more staining on the adherend or resulting in migration and staining of the emulsifier to the adherend. The reactive emulsifier, if present in an amount of less than 0.1 part by weight, may fail to maintain stable emulsification.
The polymerization initiator for use in the emulsion polymerization to form the acrylic emulsion polymer (A) is exemplified by, but is not limited to, azo polymerization initiators such as 2,2′-azobisisobutyronitrile, 2,2′-azobis(2-amidinopropane)dihydrochloride, 2,2′-azobis[2-(5-methyl-2-imidazolin-2-yl)propane]dihydrochloride, 2,2′-azobis(2-methylpropionamidine)disulfate, and 2,2′-azobis(N,N′-dimethyleneisobutylamidine); persulfate polymerization initiators such as potassium peroxodisulfate and ammonium persulfate; peroxide polymerization initiators such as benzoyl peroxide, t-butyl hydroperoxide, and hydrogen peroxide; and redox polymerization initiators each including a peroxide and a reducing agent in combination, such as redox polymerization initiators using a peroxide and ascorbic acid in combination (e.g., one using a hydrogen peroxide solution and ascorbic acid in combination), those using a peroxide and an iron(II) salt in combination (e.g., one using a hydrogen peroxide solution and an iron(II) salt), and those using a persulfate and sodium hydrogen sulfite in combination. Each of different polymerization initiators may be used alone or in combination.
The amount of the polymerization initiator(s) to be added (used) is not critical and may be determined as appropriate according to the types of the polymerization initiator(s) and the constitutive monomers, but is preferably from 0.01 to 1 part by weight, and more preferably from 0.02 to 0.5 part by weight, per 100 parts by weight of the total amount of constitutive monomers (total constitutive monomers) constituting the acrylic emulsion polymer (A).
Polymerization to form the acrylic emulsion polymer (A) may employ a chain-transfer agent so as to regulate the molecular weight of the acrylic emulsion polymer (A). The chain-transfer agent is not limited and can be any of known or customary chain-transfer agents such as lauryl mercaptan, glycidyl mercaptan, mercaptoacetic acid, 2-mercaptoethanol, thioglycolic acid, 2-ethylhexyl thioglycolate, and 2,3-dimercapto-1-propanol. Each of different chain-transfer agents may be used alone or in combination. The chain-transfer agent(s) may be incorporated (used) in an amount of preferably from 0.001 to 0.5 part by weight, per 100 parts by weight of the total amount of constitutive monomers (total constitutive monomers) constituting the acrylic emulsion polymer (A).
The emulsion polymerization to form the acrylic emulsion polymer (A) is not limited in procedure and may be performed by an arbitrary common procedure such as batch polymerization, continuous dropping polymerization, or portion-wise dropping polymerization. The polymerization is, however, preferably performed by batch polymerization at a low temperature (e.g., 55° C. or lower, preferably 30° C. or lower) for less causing staining. The polymerization, when performed under these conditions, may often give a polymer which includes high-molecular-weight components in large amounts but low-molecular-weight components in small amounts, and this may probably reduce staining.
The acrylic emulsion polymer (A) is a polymer including, as essential constitutional units, constitutional units derived from the (meth)acrylic alkyl ester, and constitutional units derived from the carboxyl-containing unsaturated monomer. The acrylic emulsion polymer (A) may contain constitutional units derived from the (meth)acrylic alkyl ester in a content of preferably from 70 to 99.5 percent by weight, more preferably from 85 to 99 percent by weight, and furthermore preferably from 91 to 98 percent by weight. The acrylic emulsion polymer (A) may contain constitutional units derived from the carboxyl-containing unsaturated monomer preferably from 0.5 to 10 percent by weight, more preferably from 1 to 5 percent by weight, and furthermore preferably from 2 to 4 percent by weight.
The acrylic emulsion polymer (A) may have a solvent-insoluble content (percentage of solvent-insoluble matter; also referred to as a “gel fraction”) of preferably 70% (percent by weight) or more, more preferably 75 percent by weight or more, and furthermore preferably 80 percent by weight or more. The acrylic emulsion polymer (A), if having a solvent-insoluble content of less than 70 percent by weight, may contain large amounts of low-molecular-weight components. Such large amounts of low-molecular-weight components may not be reduced by the action of crosslinking alone and may remain in the pressure-sensitive adhesive layer to cause stains on the adherend or to cause the pressure-sensitive adhesive layer to have an excessively high adhesive strength. The solvent-insoluble content can be controlled by conditions or parameters such as the polymerization initiator, the reaction temperature, and the types of the emulsifier and constitutive monomers. Though not critical, the upper limit of the solvent-insoluble content may be 99 percent by weight.
As used herein the term “solvent-insoluble content” of the acrylic emulsion polymer (A) refers to a value as determined by calculation according to the following “method for measuring solvent-insoluble content.”
(Method for Measuring Solvent-Insoluble Content)
About 0.1 g of the acrylic emulsion polymer (A) is sampled to give a specimen, the specimen is covered by a porous tetrafluoroethylene sheet (trade name “NTF1122” supplied by Nitto Denko Corporation) having an average pore size of 0.2 μm, tied with a kite string, and the weight of the resulting article is measured and defined as a “weight before immersion.” The weight before immersion is the total weight of the acrylic emulsion polymer (A) (the sampled specimen), the tetrafluoroethylene sheet, and the kite string. Independently, the total weight of the tetrafluoroethylene sheet and the kite string is measured and defined as a “tare weight.”
Next, the specimen acrylic emulsion polymer (A) covered by the tetrafluoroethylene sheet and tied with the kite string (this article is hereinafter referred to as “sample”) is placed in a 50-ml vessel filled with ethyl acetate and left stand therein at 23° C. for 7 days. The sample (after treatment with ethyl acetate) is recovered from the vessel, transferred to an aluminum cup, dried in a drier at 130° C. for 2 hours to remove ethyl acetate, and the weight of the resulting sample is measured and defined as a “weight after immersion.”
The solvent-insoluble content is calculated according to the following equation:
Solvent-insoluble content (percent by weight)=(a−b)/(c−b)×100 (1)
wherein “a” represents the weight after immersion; “b” represents the tare weight; and “c” represents the weight before immersion.
Though not critical, the pressure-sensitive adhesive composition according to the present invention may contain the acrylic emulsion polymer (A) in a content of preferably 80 percent by weight or more, and more preferably from 90 to 99 percent by weight, based on the total weight (100 percent by weight) of non-volatile components (solids) in the pressure-sensitive adhesive composition.
The water-insoluble crosslinking agent (B) for use in the pressure-sensitive adhesive composition according to the present invention is a water-insoluble compound which may have two or more (e.g., two to six) functional groups reactive with carboxyl group (carboxyl-reactive functional groups) in the molecule (per molecule). The water-insoluble crosslinking agent (B) preferably has three to five carboxyl-reactive functional groups per molecule. With an increasing number of carboxyl-reactive functional groups per molecule, the pressure-sensitive adhesive composition undergoes denser crosslinking. Specifically, the polymer constituting the pressure-sensitive adhesive layer has a denser crosslinking structure. This enables prevention of the spread of the pressure-sensitive adhesive layer caused by wetting after its formation. Such dense crosslinking structure may constrain the polymer constituting the pressure-sensitive adhesive layer and may avoid the segregation of the functional groups (carboxyl groups) in the pressure-sensitive adhesive layer to the surface in contact with the adherend, thus preventing increase in adhesive strength between the pressure-sensitive adhesive layer and the adherend with time. The water-insoluble crosslinking agent (B), if having carboxyl-reactive functional groups in an excessively large number of more than six, may cause the formation of a gelled substance.
Exemplary carboxyl-reactive functional groups in the water-insoluble crosslinking agent (B) include, but are not limited to, epoxy groups, isocyanate groups, and carbodiimide groups. Among them, epoxy groups are preferred for satisfactory reactivity; of which glycidylamino group is more preferred. This is because the glycidylamino group is highly reactive, thereby prevents an unreacted substance from remaining after the crosslinking reaction, and advantageously helps the pressure-sensitive adhesive sheet to less cause staining. The highly-reactive glycidylamino group also reduces the amount of unreacted carboxyl groups in the pressure-sensitive adhesive layer and prevents increase in adhesive strength to the adherend with time, which increase is caused by unreacted carboxyl groups. Specifically, the water-insoluble crosslinking agent (B) is preferably any of epoxy crosslinking agents having epoxy groups and is more preferably any of crosslinking agents having glycidylamino groups (glycidylamino crosslinking agents). The water-insoluble crosslinking agent (B), when being an epoxy crosslinking agent (particularly, a glycidylamino crosslinking agent), has epoxy groups (particularly glycidylamino groups) in a number of two or more (e.g., two to six) and preferably in a number of from three to five per molecule.
The water-insoluble crosslinking agent (B) is a water-insoluble compound. As used herein the term “water-insoluble” refers to that the compound (crosslinking agent) has a solubility of 5 parts by weight or less, per 100 parts by weight of water at 25° C. The solubility is the weight of the compound (crosslinking agent) soluble in 100 parts by weight of water. The solubility is preferably 3 parts by weight or less, and more preferably 2 parts by weight or less. Such a water-insoluble crosslinking agent, when used, hardly causes whitening as stains on the adherend and helps the pressure-sensitive adhesive layer to further less cause staining. The whitening as stains on the adherend may occur in a high-humidity environment by the action of a crosslinking agent which has not undergone crosslinking and remains in the resulting polymer. Specifically, a water-soluble crosslinking agent, if used alone as a crosslinking agent upon crosslinking and if remaining, may be readily dissolved in water and migrate into the adhered to often cause whitening as stains on the adherend. As compared to such a water-soluble crosslinking agent, the water-insoluble crosslinking agent more contributes to the crosslinking reaction (reaction with carboxyl group) and more effectively suppresses increase in adhesive strength with time. The water-insoluble crosslinking agent also exhibits high reactivity in a crosslinking reaction, thereby allows the crosslinking reaction to proceed rapidly during aging, and suppresses increase in adhesive strength to the adherend with time, which increase is caused by unreacted carboxyl groups in the pressure-sensitive adhesive layer.
The solubility of a crosslinking agent in water may be measured typically in the following manner.
Water (25° C.) and the crosslinking agent in equal amounts are mixed with a stirrer at 300 revolutions per minute (rpm) for 10 minutes, and the mixture is separated into an aqueous phase and an oily phase by centrifugal separation. Next, the aqueous phase is recovered, dried at 120° C. for one hour, a weight loss on drying is determined, from which a non-volatile content in the aqueous phases is determined. The non-volatile content is the weight (part by weight) of non-volatile components in the aqueous phase per 100 parts by weight of water.
Specific examples of the water-insoluble crosslinking agent (B) include glycidylamino crosslinking agents such as 1,3-bis(N,N-diglycidylaminomethyl)cyclohexane (e.g., trade name “TETRAD-C” supplied by Mitsubishi Gas Chemical Company, Inc.) [having a solubility of 2 parts by weight or less per 100 parts by weight of water at 25° C.] and 1,3-bis(N,N-diglycidylaminomethyl)benzene (e.g., trade name “TETRAD-X” supplied by Mitsubishi Gas Chemical Company, Inc.) [having a solubility of 2 parts by weight or less per 100 parts by weight of water at 25° C.]; and other epoxy crosslinking agents such as tris(2,3-epoxypropyl)isocyanurate (e.g., trade name “TEPIC-G” supplied by Nissan Chemical Industries, Ltd.) [having a solubility of 2 parts by weight or less per 100 parts by weight of water at 25° C.]. Each of different water-insoluble crosslinking agents (B) may be used alone or in combination.
The water-insoluble crosslinking agent (B) may be added (incorporated) as intact as a liquid or may be added after dissolving in and/or diluting with an organic solvent in the preparation of the pressure-sensitive adhesive composition according to the present invention. In the latter case, however, the organic solvent is preferably used in a minimum amount. Addition of the water-insoluble crosslinking agent (B) after being emulsified with an emulsifier is not preferred, because the emulsifier may bleed out to cause staining (particularly whitening as stains).
The water-insoluble crosslinking agent(s) (B) is incorporated in an amount (content in the pressure-sensitive adhesive composition according to the present invention) of preferably such that the carboxyl-reactive functional groups of the water-insoluble crosslinking agent (B) are present in an amount of from 0.3 to 1.3 moles per mole of carboxyl group of the carboxyl-containing unsaturated monomer(s) used as a constitutive monomer for the acrylic emulsion polymer (A). Specifically, the pressure-sensitive adhesive composition has a ratio (molar ratio) [(carboxyl-reactive functional groups)/(carboxyl groups)] of preferably from 0.3 to 1.3, more preferably from 0.4 to 1.1, and furthermore preferably from 0.5 to 1.0. The ratio is a ratio of the “total number of moles of carboxyl-reactive functional groups in total water-insoluble crosslinking agents (B)” to the “total number of moles of carboxyl groups in all carboxyl-containing unsaturated monomers used as constitutive monomers for the acrylic emulsion polymer (A).” If the ratio [(carboxyl-reactive functional groups)/(carboxyl groups)] is less than 0.3, a large amount of unreacted carboxyl groups may remain in the pressure-sensitive adhesive layer and may interact with the adherend to increase the adhesive strength with time. If the ratio [(carboxyl-reactive functional groups)/(carboxyl groups)] is more than 1.3, a large amount of unreacted water-insoluble crosslinking agent (B) may remain in the pressure-sensitive adhesive layer to cause appearance defects.
When the water-insoluble crosslinking agent (B) is an epoxy crosslinking agent, the ratio (by mole) of [(epoxy groups)/(carboxyl groups)] is preferably from 0.3 to 1.3, more preferably from 0.4 to 1.1, and furthermore preferably from 0.5 to 1.0. When the water-insoluble crosslinking agent (B) is a glycidylamino crosslinking agent, the ratio (by mole) of [glycidylamino group/carboxyl group] preferably falls within the above-specified range.
The number of moles of carboxyl-reactive functional groups of the water-insoluble crosslinking agent (B) may be calculated according to the following equation, assuming that 4 grams of a water-insoluble crosslinking agent (B) having a functional-group equivalent of carboxyl-reactive functional groups of 110 (g/eq) is added (incorporated) to the pressure-sensitive adhesive composition:
Number of moles of carboxyl-reactive functional groups of water-insoluble crosslinking agent (B)=[Amount of water-insoluble crosslinking agent (B) to be added (incorporated)]/[Functional-group equivalent]=4/110
Typically, the number of moles of epoxy groups of an epoxy crosslinking agent may be calculated according to the following equation, assuming that 4 grams of an epoxy crosslinking agent having an epoxy equivalent of 110 (g/eq) is added (incorporated) as the water-insoluble crosslinking agent (B):
Number of moles of epoxy groups of epoxy crosslinking agent=[Amount of epoxy crosslinking agent to be added (incorporated)]/[Epoxy equivalent]=4/110
The acetylenic diol compound (C) for use in the pressure-sensitive adhesive composition according to the present invention is a diol compound having an acetylene bond in the molecule. Preferred examples of the acetylenic diol compound (C) include, but are not limited to, a compound represented by Formula (IV) and a compound represented by Formula (V) below.
Specifically, preferred examples of the acetylenic diol compound (C) include a compound represented by following Formula (IV):
In Formula (IV), each of R1, R2, R3, and R4 independently represents a hydrocarbon group having 1 to 20 carbon atoms, which may contain one or more heteroatoms. The substituents R1, R2, R3, and R4 may be the same as or different from one another.
Each of R1, R2, R3 and R4 in Formula (IV) may have a linear or branched chain structure. Among them, each of R1 and R4 is preferably an alkyl group having 2 to 10 carbon atoms, and is more preferably an alkyl group having 4 carbon atoms, i.e., n-butyl group, sec-butyl group, tert-butyl group, or isobutyl group. Each of R2 and R3 is preferably an alkyl group having 1 to 4 carbon atoms, and is more preferably an alkyl group having 1 or 2 carbon atoms, i.e., methyl group or ethyl group.
Examples of the acetylenic diol compound (C) represented by Formula (IV) include 7,10-dimethyl-8-hexadecyne-7,10-diol, 4,7-dimethyl-5-decyne-4,7-diol, 2,4,7,9-tetramethyl-5-decyne-4,7-diol, and 3,6-dimethyl-4-octyne-3,6-diol.
The acetylenic diol compound (C) represented by Formula (IV) may be blended as a dispersion or solution in a solvent (medium) in the preparation of the pressure-sensitive adhesive composition according to the present invention, for better workability in blending. The solvent may be exemplified by 2-ethylhexanol, butyl cellosolve, dipropylene glycol, ethylene glycol, propylene glycol, n-propanol, and isopropyl alcohol. Among these solvents, ethylene glycol and/or propylene glycol is preferably employed for good dispersibility in the emulsion system. The content of the solvent in the dispersion or solution for use in the blending is preferably less than 40 percent by weight (e.g., from 15 to 35 percent by weight) upon the use of ethylene glycol as the solvent, and is preferably less than 70 percent by weight (e.g., from 20 to 60 percent by weight) upon the use of propylene glycol as the solvent, each based on the total amount (100 percent by weight) of the dispersion or solution of the acetylenic diol compound (C).
The acetylenic diol compound (C) represented by Formula (IV) is also available as commercial products such as SURFYNOL 104 Series products supplied by Air Products and Chemicals Inc., which are exemplified by SURFYNOL 104E, SURFYNOL 104H, SURFYNOL 104A, SURFYNOL 104BC, SURFYNOL 104DPM, SURFYNOL 104PA, and SURFYNOL 104PG-50.
Preferred examples of the acetylenic diol compound (C) also include a compound represented by following Formula (V):
In Formula (V), each of R5, R6, R7, and R8 independently represents a hydrocarbon group having 1 to 20 carbon atoms, which may contain one or more heteroatoms. The substituents R5, R6, R7, and R8 may be the same as or different from one another. The repetition numbers p and q in Formula (V) are each independently an integer of 0 or more, where the total [p+q] of p and q is 1 or more, and is preferably from 1 to 20 and more preferably from 1 to 9. The repetition numbers p and q may be the same as or different from each other. The numbers p and q are regulated so that the acetylenic diol compound (C) has an HLB of less than 13. When p is 0, the group [—O—(CH2CH2O)pH] is hydroxyl group [—OH]; and the same is true for q.
Each of R5, R6, R7, and R8 in Formula (V) may have a linear or branched chain structure. Among them, each of R5 and R8 is preferably an alkyl group having 2 to 10 carbon atoms, and is more preferably an alkyl group having 4 carbon atoms, i.e., n-butyl group, sec-butyl group, tert-butyl group, or isobutyl group. Each of R6 and R7 is preferably an alkyl group having 1 to 4 carbon atoms, and is more preferably an alkyl group having 1 or 2 carbon atoms, i.e., methyl group or ethyl group.
Examples of the acetylenic diol compound (C) represented by Formula (V) include an ethylene oxide adduct of 7,10-dimethyl-8-hexadecyne-7,10-diol, an ethylene oxide adduct of 4,7-dimethyl-5-decyne-4,7-diol, an ethylene oxide adduct of 2,4,7,9-tetramethyl-5-decyne-4,7-diol, and an ethylene oxide adduct of 3,6-dimethyl-4-octyne-3,6-diol. The average number of moles of ethylene oxide added in the ethylene oxide adduct of 2,4,7,9-tetramethyl-5-decyne-4,7-diol is preferably 9 or less.
The repetition numbers p and q in Formula (V) are regulated so that the acetylenic diol compound (C) has an HLB of less than 13. For example, the total of p and q is preferably 9 or less when the acetylenic diol compound (C) represented by Formula (V) is an ethylene oxide adduct of 2,4,7,9-tetramethyl-5-decyne-4,7-diol.
The acetylenic diol compound (C) represented by Formula (V) (acetylenic diol ethylene oxide adduct) is preferably blended alone without the use of a solvent in the preparation of the pressure-sensitive adhesive composition according to the present invention. However, for better blending workability, the acetylenic diol compound (C) may be used as a dispersion or solution in a solvent. The solvent herein is exemplified by 2-ethylhexanol, butyl cellosolve, dipropylene glycol, ethylene glycol, propylene glycol, n-propanol, and isopropyl alcohol. Among these solvents, ethylene glycol and/or propylene glycol is preferably employed for satisfactory dispersibility in the emulsion system.
The acetylenic diol compound (C) represented by Formula (V) may also be any of commercial products such as SURFYNOL 400 Series products supplied by Air Products and Chemicals Inc., which are exemplified by SURFYNOL 420 and SURFYNOL 440.
Each of different acetylenic diol compounds (C) may be used alone or in combination.
The acetylenic diol compound (C) has a hydrophile-lypophile balance (also simply referred to as “HLB”) of less than 13, preferably from 1 to 10, more preferably from 3 to 8, and furthermore preferably from 3 to 5. An acetylenic diol compound having an HLB of 13 or more may cause stains on the adherend. The HLB is a hydrophile-lypophile balance defined by Griffin and indicates the degree of affinity of a surfactant for water and for oils. The definition of the HLB is described by W. C. Griffin in J. Soc. Cosmetic Chemists, 1, 311 (1949) and by Koshitami TAKAHASHI, Yoshiro NAMBA, Motoo KOIKE, and Masao KOBAYASHI in “Handbook of Surfactants,” 3rd Ed., Kogaku Tosho K.K., Tokyo Japan, Nov. 25, 1972, pp. 179-182.
The acetylenic diol compound(s) (C) may be blended in an amount (content in the pressure-sensitive adhesive composition according to the present invention) of preferably from 0.01 to 10 parts by weight, more preferably from 0.1 to 7 parts by weight, and furthermore preferably from 0.5 to 5 parts by weight, per 100 parts by weight of the acrylic emulsion polymer (A). The acetylenic diol compounds (C), if present in an amount of less than 0.01 part by weight, may not exhibit sufficient activity of suppressing appearance defects due to dimples caused by the water-insoluble crosslinking agent; and the acetylenic diol compounds (C), if present in an amount of more than 10 parts by weight, may stain the adherend.
The acetylenic diol compound (C), when blended, may suppress the occurrence of dimples as defects derived from the water-insoluble crosslinking agent. This is probably because the acetylenic diol compounds (C) may help the water-insoluble crosslinking agent to be more satisfactorily dispersed in the pressure-sensitive adhesive composition and may exhibit a leveling activity upon the formation of the pressure-sensitive adhesive layer.
The polyether defoaming agent (D) for use in the pressure-sensitive adhesive composition according to the present invention is a compound (at least one compound) selected from the group consisting of compounds represented by Formula (I), compounds represented by Formula (II), and compounds represented by Formula (III). The polyether defoaming agent (D) may be obtained by allowing a fatty acid or a higher alcohol to react with propylene oxide or with ethylene oxide and propylene oxide; or by allowing ethylene glycol to react with propylene glycol.
As used herein the symbol PO represents oxypropylene group [—CH2CH(CH3)O—]; and the symbol EO represents oxyethylene group [—CH2CH2O—].
Examples of the polyether defoaming agent (D) include compounds represented by following Formula (I):
RaO—(PO)n1(EO)m1—CO—Rb (I)
In Formula (I), Ra represents an alkyl or alkenyl group having 8 to 22 carbon atoms, or an alkylcarbonyl or alkenylcarbonyl group having 8 to 21 carbon atoms; and Rb represents an alkyl or alkenyl group having 8 to 21 carbon atoms.
In Formula (I), PO represents oxypropylene group; and EO represents oxyethylene group. The repetition number n1 denotes an integer of 1 or more, may be suitably adjusted so as to allow the polyether defoaming agent (D) to have a PO content of from 70 to 100 percent by weight, but is preferably from 2 to 50. The repetition number m1 denotes an integer of from 0 to 15 and is preferably an integer of from 2 to 10. When m1 is 0, the compound of Formula (I) is represented by RaO—(PO)n1—CO—Rb.
EO and PO in Formula (I) are added (copolymerized) in a random manner or block manner. When they are added in a block manner, exemplary arrangement of respective blocks are (EO block)-(PO block)-(EO block); (PO block)-(EO block)-(PO block); (EO block)-(PO block); and (PO block)-(EO block).
Examples of the polyether defoaming agent (D) also include compounds represented by following Formula (II):
RcO—(PO)n2(EO)m2—H (II)
In Formula (II), Ro represents nonylphenyl group, octylphenyl group, or an alkyl or alkenyl group having 8 to 22 carbon atoms.
In Formula (II), PO represents oxypropylene group; and EO represents oxyethylene group. The repetition number n2 denotes an integer of 1 or more, may be suitable adjusted so as to allow the polyether defoaming agent (D) to have a PO content of from 70 to 100 percent by weight, but is preferably from 10 to 40. The repetition number m2 denotes an integer of from 0 to 20 and is preferably an integer of from 2 to 10. When m2 is 0, the compound of Formula (II) is represented by RcO—(PO)n2—H.
EO and PO in Formula (II) are added (polymerized) in a random manner or block manner. When they are added in a block manner, exemplary arrangements of respective blocks are (EO block)-(PO block); and (PO block)-(EO block).
Examples of the polyether defoaming agent (D) still also include compounds represented by following Formula (III).
HO—(PO)n3(EO)m3—H (III)
In Formula (III), PO represents oxypropylene group; and EO represents oxyethylene group. The repetition number n3 denotes an integer of 1 or more, may be suitably adjusted so as to allow the polyether defoaming agent (D) to have a PO content of from 70 to 100 percent by weight, but is preferably from 10 to 69. The repetition number m3 denotes an integer of from 0 to 40 and is preferably an integer of from 2 to 27. When m3 is 0, the compound represented by Formula (III) is a polypropylene glycol represented by HO—(PO)n3—H.
EO and PO in Formula (III) are added (copolymerized) in a random manner or block manner. When they are added in a block manner, exemplary arrangements of respective blocks include (EO block)-(PO block)-(EO block); (PO block)-(EO block)-(PO block); (EO block)-(PO block); and (PO block)-(EO block).
Each of different polyether defoaming agents (D) may be used alone or in combination.
Of the polyether defoaming agents (D), compounds represented by Formula (III) are preferred particularly for good balance between defoaming activity and less-staining properties. Among them, a compound represented by Formula (III), in which EO and PO are added (copolymerized) in a block manner and respective blocks are arranged as (PO block)-(EO block)-(PO block), is more preferred. Specifically, the polyether defoaming agent (D) is preferably a triblock copolymer having an EO block and, on both sides thereof, PO blocks.
The polyether defoaming agent (D) can be any of commercial products marketed as defoaming agents. Exemplary commercial products include products available under the trade names “PLONON #101P,” “PLONON #183,” “PLONON #201,” “PLONON #202B,” “PLONON #352,” “UNILUBE 10MS-250 KB,” and “UNILUBE 20MT-2000B” each from NOF CORPORATION; and products available under the trade names “ADEKA PLURONIC L-33,” “ADEKA PLURONIC L-42,” “ADEKA PLURONIC L-43,” “ADEKA PLURONIC L-61,” “ADEKA PLURONIC L-62,” “ADEKA PLURONIC L-71,” “ADEKA PLURONIC L-72,” “ADEKA PLURONIC L-81,” “ADEKA PLURONIC L-92,” “ADEKA PLURONIC L-101,” “ADEKA PLURONIC 17R-2,” “ADEKA PLURONIC 17R-3,” “ADEKA PLURONIC 25R-1,” and “ADEKA PLURONIC 25R-2” each from ADEKA CORPORATION.
The polyether defoaming agent (D) has a propylene oxide content (also referred to as a “PO content”) of 70 to 100 percent by weight, preferably from 70 to 95 percent by weight, more preferably from 80 to 95 percent by weight, furthermore preferably from 85 to 95 percent by weight, and most preferably from 90 to 95 percent by weight, based on the total amount (100 percent by weight) of the polyether defoaming agent (D). A polyether defoaming agent having a PO content of less than 70 percent by weight may cause staining on the adherend. The polyether defoaming agent (D) has a PO content of preferably 95 percent by weight or less, for less causing stains. The term “PO content” as used herein refers to “a ratio (percent by weight) of the total weight of POs (oxypropylene groups) in all polyether defoaming agents (D) contained in the pressure-sensitive adhesive composition according to the present invention to the total weight of all the polyether defoaming agents (D).” The PO content may be measured typically by nuclear magnetic resonance analysis (NMR).
The polyether defoaming agent (D) has a number-average molecular weight (Mn) of from 1200 to 4000 and preferably from 1500 to 3500. A polyether defoaming agent having a number-average weight Mn of more than 4000 may cause staining on the adherend. A polyether defoaming agent having a number-average weight Mn of less than 1200 may also cause staining on the adherend. The term “number-average molecular weight (Mn)” refers to the number-average molecular weight of all polyether defoaming agents (D) contained in the pressure-sensitive adhesive composition according to the present invention. The “number-average molecular weight (Mn)” refers to a value determined by measurement through gel permeation chromatography (GPC). The measurement may be performed, for example, by the following method.
The molecular weight is measured with the GPC system “HLC-8220GPC” supplied by Tosoh Corporation and determined in terms of polystyrene standard. The measurement is performed under the following conditions:
Sample concentration: 0.2 percent by weight (tetrahydrofuran (THF) solution)
Sample volume: 10 μl
Eluent: THF
Flow rate: 0.6 ml/min
Measurement temperature: 40° C.
Columns: Sample columns; one TSKguardcolumn SuperHZ-H column and two TSKgel SuperHZM-H columns
The polyether defoaming agent(s) (D) may be contained in an amount (content in the pressure-sensitive adhesive composition according to the present invention) of preferably from 0.01 to 2.5 parts by weight, more preferably from 0.01 to 1.5 parts by weight, furthermore preferably from 0.02 to 1.0 parts by weight, still more preferably from 0.02 to 0.5 part by weight, and most preferably from 0.02 to 0.3 parts by weight, per 100 parts by weight of the acrylic emulsion polymer (A). The polyether defoaming agent (D), if present in an amount of less than 0.01 part by weight, may not impart sufficient defoaming activity to the pressure-sensitive adhesive composition (may not sufficiently prevent appearance defects derived from bubbles). The polyether defoaming agent (D), if present in an amount of more than 2.5 parts by weight, may often cause staining on the adherend.
The removable water-dispersible acrylic pressure-sensitive adhesive composition according to the present invention contains the acrylic emulsion polymer (A), the water-insoluble crosslinking agent (B), the acetylenic diol compound (C), and the polyether defoaming agent (D) as essential components, as described above. Where necessary, the composition may further contain a crosslinking agent other than the water-insoluble crosslinking agent (B) (hereinafter also referred to as “other crosslinking agent”), a polyoxyalkylene compound other than the polyether defoaming agent (D) (hereinafter also referred to as “other polyoxyalkylene compound”), and other additive.
The pressure-sensitive adhesive composition according to the present invention is a water-dispersible pressure-sensitive adhesive composition. The term “water-dispersible” refers to that the composition is dispersible in an aqueous medium. Specifically, the pressure-sensitive adhesive composition according to the present invention is a pressure-sensitive adhesive composition which is dispersible in an aqueous medium. The aqueous medium is a medium (dispersion medium) which contains water as an essential component and may contain water alone or a mixture of water and a water-soluble (water-miscible) organic solvent. The pressure-sensitive adhesive composition according to the present invention may also be a fluid dispersion using the aqueous medium.
The pressure-sensitive adhesive composition according to the present invention may further contain another crosslinking agent (other crosslinking agent) than the water-insoluble crosslinking agent (B). Though not limited, the other crosslinking agent is preferably a multifunctional hydrazide crosslinking agent. The use of the multifunctional hydrazide crosslinking agent may help the pressure-sensitive adhesive layer formed from the pressure-sensitive adhesive composition to have better removability, more satisfactory adhesiveness, and higher anchoring capability to the substrate. The multifunctional hydrazide crosslinking agent (hereinafter also simply referred to as “hydrazide crosslinking agent”) is a compound having at least two hydrazide groups in the molecule (per molecule). The hydrazide crosslinking agent preferably has two or three hydrazide groups, and more preferably has two hydrazide groups per molecule. Exemplary compounds preferably used as the hydrazide crosslinking agent include, but are not limited to, dihydrazide compounds such as oxalic acid dihydrazide, malonic acid dihydrazide, succinic acid dihydrazide, glutaric acid dihydrazide, adipic acid dihydrazide, pimelic acid dihydrazide, suberic acid dihydrazide, azelaic acid dihydrazide, sebacic acid dihydrazide, dodecanedioic acid dihydrazide, phthalic acid dihydrazide, isophthalic acid dihydrazide, terephthalic acid dihydrazide, 2,6-naphthalenedicarboxylic acid dihydrazide, naphthalic acid dihydrazide, acetonedicarboxylic acid dihydrazide, fumaric acid dihydrazide, maleic acid dihydrazide, itaconic acid dihydrazide, trimellitic acid dihydrazide, 1,3,5-benzenetricarboxylic acid dihydrazide, pyromellitic acid dihydrazide, and aconitic acid dihydrazide. Among them, adipic acid dihydrazide and sebacic acid dihydrazide are particularly preferred. Each of different hydrazide crosslinking agents may be used alone or in combination.
The hydrazide crosslinking agent is also available as commercial products such as products available as “Adipic Acid Dihydrazide (Reagent)” from Tokyo Chemical Industry Co., Ltd. and as “Adipoyl Dihydrazide (Reagent)” from Wako Pure Chemical Industries, Ltd.
The hydrazide crosslinking agent may be contained in an amount (content in the pressure-sensitive adhesive composition according to the present invention) of preferably from 0.025 to 2.5 moles, more preferably from 0.1 to 2 moles, and furthermore preferably from 0.2 to 1.5 moles, per mole of keto groups of the keto-containing unsaturated monomer used as a constitutive monomer for the acrylic emulsion polymer (A). The hydrazide crosslinking agent, if present in an amount of less than 0.025 mole, may not exhibit sufficient effects. This may cause the pressure-sensitive adhesive layer or pressure-sensitive adhesive sheet to be peeled off heavily (with less releasability) and may cause low-molecular-weight components to remain in the polymer constituting the pressure-sensitive adhesive layer to often cause whitening as stains on the adherend. The hydrazide crosslinking agent, if present in an amount of more than 2.5 moles, may remain as an unreacted crosslinking agent component to cause staining.
The pressure-sensitive adhesive composition according to the present invention may further contain another polyoxyalkylene compound (also referred to as “other polyoxyalkylene compound”) than the polyether defoaming agent (D), for furthermore satisfactory defoaming activity. Examples of the other polyoxyalkylene compound include reaction products of a monoalcohol having 4 to 18 carbon atoms, a monocarboxylic acid having 4 to 18 carbon atoms, or a monoamine having 4 to 18 carbon atoms with an alkylene oxide having 2 or 4 carbon atoms; and reaction products of a polyol having 3 to 60 carbon atoms with an alkylene oxide having 2 or 4 carbon atoms. The monoalcohol having 4 to 18 carbon atoms is exemplified by butyl alcohol, isoamyl alcohol, n-amyl alcohol, hexyl alcohol, heptyl alcohol, octyl alcohol, capryl alcohol, nonyl alcohol, decyl alcohol, undecyl alcohol, lauryl alcohol, tridecyl alcohol, myristyl alcohol, pentadecyl alcohol, cetyl alcohol, heptadecyl alcohol, and stearyl alcohol. The monocarboxylic acid having 4 to 18 carbon atoms is exemplified by butyric acid, valeric acid, capric acid, enanthic acid, caprylic acid, pelargonic acid, undecylic acid (undecanoic acid), lauric acid, tridecylic acid (tridecanoic acid), myristic acid, pentadecylic acid (pentadecanoic acid), palmitic acid, heptadecylic acid (heptadecanoic acid), and stearic acid. The monoamine having 4 to 18 carbon atoms is exemplified by butylamine, octylamine, laurylamine, and stearylamine. The polyol having 3 to 60 carbon atoms is typified by glycerol, trimethylolpropane, trimethylolbutane, pentaerythritol, condensates of phenol or an alkylphenol (e.g., octylphenol, nonylphenol, or butylphenol) with formaldehyde, and sugars such as glycoside, sucrose, isosucrose, trehalose, isotrehalose, gentianose, melezitose, planteose, and raffinose.
The other polyoxyalkylene compound may be contained in a content of preferably 120 parts by weight or less, more preferably from 1 to 115 parts by weight, furthermore preferably from 3 to 110 parts by weight, and most preferably from 5 to 100 parts by weight, per 100 parts by weight of the polyether defoaming agent (D).
For less staining, the pressure-sensitive adhesive composition according to the present invention is preferably incorporated with no quaternary ammonium salt and more preferably incorporated with no quaternary ammonium compound. Specifically, the pressure-sensitive adhesive composition according to the present invention preferably contains substantially no quaternary ammonium salt and more preferably contains substantially no quaternary ammonium compound. These compounds are generally used as catalysts for improving the reactivity of epoxy crosslinking agents. The compounds, however, are not integrated into the polymer constituting the pressure-sensitive adhesive layer, can migrate freely in the pressure-sensitive adhesive layer, and are liable to precipitate to the adherend surface. For these reasons, the pressure-sensitive adhesive composition, if containing any of the compounds, may often cause whitening as stains to fail to less cause staining. Specifically, the pressure-sensitive adhesive composition according to the present invention has a quaternary ammonium salt content of preferably less than 0.1 percent by weight, more preferably less than 0.01 percent by weight, and furthermore preferably less than 0.005 percent by weight, based on the total weight (100 percent by weight) of non-volatile components in the pressure-sensitive adhesive composition. More preferably, the pressure-sensitive adhesive composition has a quaternary ammonium compound content falling within the above-specified range.
Examples of the quaternary ammonium salt include, but are not limited to, compounds represented by the following formula:
In the formula, each of R9, R10, R11, and R12 independently represents not hydrogen atom, but an alkyl group, an aryl group, or a group derived from them (e.g., a substituted alkyl or aryl group); and X− represents a counter ion.
The quaternary ammonium salt and the quaternary ammonium compound are typified by, but are not limited to, alkylammonium hydroxides such as tetramethylammonium hydroxide (TMAH), tetraethylammonium hydroxide, tetrapropylammonium hydroxide, and tetrabutylammonium hydroxide, and salts of them; arylammonium hydroxides such as tetraphenylammonium hydroxide, and salts of them; and bases and salts of them, which bases include, as a cation, any of trilaurylmethylammonium ion, didecyldimethylammonium ion, dicocoyldimethylammonium ion, distearyldimethylammonium ion, dioleyldimethylammonium ion, cetyltrimethylammonium ion, stearyltrimethylammonium ion, behenyltrimethylammonium ion, cocoylbis(2-hydroxyethyl)methylammonium ion, polyoxyethylene(15) cocostearylmethylammonium ion, oleylbis(2-hydroxyethyl)methylammonium ion, cocobenzyldimethylammonium ion, laurylbis(2-hydroxyethyl)methylammonium ion, and decylbis(2-hydroxyethyl)methylammonium ion.
Also for less staining, the pressure-sensitive adhesive composition according to the present invention is preferably incorporated with neither tertiary amines nor imidazole compounds. Such tertiary amines and imidazole compounds are generally used as catalysts for improving the reactivity of epoxy crosslinking agents as with the quaternary ammonium salts (or quaternary ammonium compounds). The pressure-sensitive adhesive composition according to the present invention therefore preferably contains substantially no tertiary amine and substantially no imidazole compound. Specifically, the pressure-sensitive adhesive composition according to the present invention has a content of tertiary amines and imidazole compounds (total content of tertiary amines and imidazole compounds) of preferably less than 0.1 percent by weight, more preferably less than 0.01 percent by weight, and furthermore preferably less than 0.005 percent by weight, based on the total weight (100 percent by weight) of non-volatile components in the pressure-sensitive adhesive composition.
The tertiary amines include tertiary amine compounds such as triethylamine, benzyldimethylamine, and α-methylbenzyl-dimethylamine. The imidazole compounds include 2-methylimidazole, 2-heptadecylimidazole, 2-phenylimidazole, 4-ethylimidazole, 4-dodecylimidazole, 2-phenyl-4-hydroxymethylimidazole, 2-ethyl-4-hydroxymethylimidazole, 1-cyanoethyl-4-methylimidazole, and 2-phenyl-4,5-dihydroxymethylimidazole.
The pressure-sensitive adhesive composition preferably contains substantially no hydrophobic silica. Specifically, the pressure-sensitive adhesive composition has a hydrophobic silica content of preferably less than 5×10−4 percent by weight, more preferably less than 1×10−4 percent by weight, furthermore preferably less than 1×10−5 percent by weight, and most preferably 0 percent by weight, based on the total weight (100 percent by weight) of non-volatile components in the pressure-sensitive adhesive composition. Hydrophobic silica, if contained in the pressure-sensitive adhesive composition, may form secondary aggregates, and the resulting silica particles (aggregates) may cause a defect (appearance defect). In addition, the silica particles may clog a filter upon filtration of the pressure-sensitive adhesive composition through the filter, resulting in insufficient production efficiency.
The pressure-sensitive adhesive composition according to the present invention may further contain any of other additives than those mentioned above, within ranges not adversely affecting less-staining properties. Exemplary other additives include pigments, fillers, dispersing agents, plasticizers, stabilizers, antioxidants, ultraviolet absorbers, ultraviolet stabilizers, age inhibitors, and antiseptic agents.
The pressure-sensitive adhesive composition according to the present invention may be prepared by mixing the acrylic emulsion polymer (A), the water-insoluble crosslinking agent (B), the acetylenic diol compound (C), and the polyether defoaming agent (D) with one another. Where necessary, any of other crosslinking agents, other polyoxyalkylene compounds, and other additives may further be mixed therewith. The mixing may be performed according to any known or customary process for mixing an emulsion with other components, but is preferably performed by stirring with a stirrer. The stirring is not limited in conditions, but may be performed at a temperature of preferably from 10° C. to 50° C. and more preferably from 20° C. to 35° C. for a duration of preferably from 5 to 30 minutes and more preferably from 10 to 20 minutes, at a rate (number of revolutions) of preferably from 10 to 2000 rpm and more preferably from 30 to 1000 rpm.
The pressure-sensitive adhesive composition thus obtained is applied to at least one side (surface) of a substrate (also referred to as a “base material” or “supporting substrate”), dried according to necessity to form a pressure-sensitive adhesive layer, and yields a pressure-sensitive adhesive sheet according to the present invention. This is a pressure-sensitive adhesive sheet including a substrate and, on at least one side thereof, a pressure-sensitive adhesive layer formed from the pressure-sensitive adhesive composition according to the present invention. Crosslinking may be performed typically by heating the pressure-sensitive adhesive sheet after dehydration and drying in the drying step. The pressure-sensitive adhesive layer herein is preferably formed by a so-called direct application process, in which the pressure-sensitive adhesive composition is directly applied to the surface of the substrate, as described above. This is because the pressure-sensitive adhesive layer herein has a high solvent-insoluble content and, if formed by a transfer process, may not exhibit sufficient anchoring capability (adhesion) to the substrate. In the transfer process, a pressure-sensitive adhesive layer is once provided on a release film and then transferred onto the substrate. It should be noted, however, that the pressure-sensitive adhesive sheet according to the present invention has only to be a pressure-sensitive adhesive sheet having a substrate and, at least on one side thereof, a pressure-sensitive adhesive layer formed from the pressure-sensitive adhesive composition according to the present invention, and is not limited in its production method.
The pressure-sensitive adhesive layer (after crosslinking) in the pressure-sensitive adhesive sheet according to the present invention has a thickness of preferably from 1 to 50 μm, more preferably from 1 to 35 μm, and furthermore preferably from 3 to 25 μm.
The pressure-sensitive adhesive layer (after crosslinking) in the pressure-sensitive adhesive sheet according to the present invention has a solvent-insoluble content (gel fraction) of preferably 90% (percent by weight) or more, and more preferably 95 percent by weight or more. The pressure-sensitive adhesive layer, if having a solvent-insoluble content of less than 90 percent by weight, may cause contaminants (staining substances) to migrate into the adherend to thereby cause whitening as stains or may have insufficient removability to cause heavy peeling.
The solvent-insoluble content of the pressure-sensitive adhesive layer (after crosslinking) can be measured by the procedure of the method for measuring the solvent-insoluble content of the acrylic emulsion polymer (A). Specifically, the solvent-insoluble content herein may be measured by the procedure corresponding to the “method for measuring solvent-insoluble content,” except that the term “acrylic emulsion polymer (A)” is read as “pressure-sensitive adhesive layer (after crosslinking).”
The pressure-sensitive adhesive layer (after crosslinking) in the pressure-sensitive adhesive sheet has an elongation at break (elongation at rupture) in a tensile test of preferably 200% or less, more preferably 150% or less, furthermore preferably 130% or less, still more preferably from 40% to 120%, and most preferably from 60% to 115%, for a suitable degree of crosslinking of the pressure-sensitive adhesive layer. The elongation at break is an index of the degree of crosslinking of the pressure-sensitive adhesive layer and, if being 200% or less, the polymer constituting the pressure-sensitive adhesive layer may have a dense crosslinking structure. This enables the prevention of spread by wetting of the pressure-sensitive adhesive layer after its formation. Such dense crosslinking structure may constrain the polymer constituting the pressure-sensitive adhesive layer and may prevent the segregation of the functional groups (carboxyl groups) in the pressure-sensitive adhesive layer to the surface in contact with the adherend, thus preventing increase in adhesive strength to the adherend with time.
The acrylic polymer (after crosslinking) constituting the pressure-sensitive adhesive layer in the pressure-sensitive adhesive sheet according to the present invention has a glass transition temperature of preferably from −70° C. to −10° C., more preferably from −70° C. to −20° C., furthermore preferably from −70° C. to −40° C., and most preferably from −70° C. to −60° C. The acrylic polymer, if having a glass transition temperature of higher than −10° C., may cause the pressure-sensitive adhesive layer to have an insufficient adhesive strength to thereby suffer from gaps and/or separation upon working. The acrylic polymer, if having a glass transition temperature of lower than −70° C., may cause the pressure-sensitive adhesive layer to suffer from heavy peeling when peeled off at higher peel rates (at higher tensile speeds), thus inviting insufficient working efficiency. The glass transition temperature of the acrylic polymer (after crosslinking) constituting the pressure-sensitive adhesive layer may also be controlled typically by the monomer formulation upon the preparation of the acrylic emulsion polymer (A).
The substrate for use in the pressure-sensitive adhesive sheet according to the present invention is preferably a plastic substrate (e.g., a plastic film or plastic sheet) for allowing the pressure-sensitive adhesive sheet to have high transparency. Exemplary materials for the plastic substrate include, but are not limited to, transparent resins including polyolefins (polyolefin resins) such as polypropylenes and polyethylenes; polyesters (polyester resins) such as poly(ethylene terephthalate)s (PETs); polycarbonates; polyamides; polyimides; acrylic resins; polystyrenes; acetate resins; polyethersulfones; and triacetyl cellulose resins. Each of such resins may be used alone or in combination. Though not limited, polyester resins and polyolefin resins are preferred among these resins, of which PETs, polypropylenes, and polyethylenes are more preferred for satisfactory productivity and moldability (formability). Specifically, the substrate is preferably any of polyester films and polyolefin films and is more preferably any of PET films, polypropylene films, and polyethylene films. The polypropylenes are typified by, but are not limited to, homopolypropylenes as homopolymers; random polypropylenes as α-olefin random copolymers; and block polypropylenes as α-olefin block copolymers. The polyethylenes are typified by low-density polyethylenes (LDPEs), high-density polyethylenes (HDPEs), and linear low-density polyethylenes (L-LDPEs). Each of these may be used alone or in combination. Though not critical, the substrate has a thickness of preferably from 10 to 150 μm, and more preferably from 30 to 100 μm.
The surface of the substrate, on which the pressure-sensitive adhesive layer is to be provided, preferably has undergone an adhesion-promoting treatment such as acid treatment, base treatment, primer treatment, corona treatment, plasma treatment, or ultraviolet treatment typically for improving the adhesion to the pressure-sensitive adhesive layer. The pressure-sensitive adhesive sheet may further include an intermediate layer between the substrate and the pressure-sensitive adhesive layer. The intermediate layer has a thickness of preferably from 0.05 to 1 μm, and more preferably from 0.1 to 1 μm.
The pressure-sensitive adhesive sheet according to the present invention has an adhesive strength of preferably from 0.01 to 5 N/25 mm, more preferably from 0.02 to 3 N/25 mm, furthermore preferably from 0.03 to 2 N/25 mm, and most preferably from 0.04 to 1 N/25 mm. The adhesive strength is a peel strength measured in a 180-degree peel test, in which the pressure-sensitive adhesive sheet is once affixed to a polarizing plate (triacetyl cellulose (TAC) plate) (one having an arithmetic mean surface roughness Ra of 50 nm or less) and then peeled off from the polarizing plate at a tensile speed of 0.3 m/min. The pressure-sensitive adhesive sheet, if having an adhesive strength of more than 5 N/25 mm, may be excessively resistant to peeling off (may have insufficient removability) to cause insufficient productivity and handleability in production process of polarizing plates and liquid crystal display devices. The pressure-sensitive adhesive sheet, if having an adhesive strength of less than 0.01 N/25 mm, may suffer from gaps and/or separation and may exhibit an insufficient protecting capability as a surface-protecting pressure-sensitive adhesive sheet in the production process. The arithmetic mean surface roughness Ra may be measured typically by using the stylus-type surface profilometer “P-15” supplied by KLA-Tencor Corporation. Though measurement conditions are not limited, the surface roughness (arithmetic mean surface roughness Ra) may be measured in one scanning pass at a measurement length of 1000 μm and a scanning speed of 50 μm/second under a load of 2 mg.
The pressure-sensitive adhesive sheet according to the present invention satisfactorily less causes whitening as stains on the adherend. This may be evaluated typically in the following manner. The pressure-sensitive adhesive sheet is affixed to a polarizing plate (trade name “SEG1425DUHC” supplied by Nitto Denko Corporation) at a pressure (load) of 0.25 MPa and a rate of 0.3 m/min., left stand at 80° C. for 4 hours, and removed from the polarizing plate. The polarizing plate after the removal of the pressure-sensitive adhesive sheet is further left stand in an environment of 23° C. and 90% relative humidity for 12 hours, and the surface of which is observed. In this observation, preferably no whitening is observed in the surface of the polarizing plate. A pressure-sensitive adhesive sheet, if causing whitening of the adherend polarizing plate under high-humidity conditions after affixation and removal of the sheet, may stain the adherend to such an extent unsuitable as a surface-protecting film for an optical member.
The pressure-sensitive adhesive sheet may be formed into a roll. In this case, the sheet may be wound as a roll with the pressure-sensitive adhesive layer being protected by a release film (separator). The pressure-sensitive adhesive sheet may have a backing layer (e.g., release layer or antifouling layer) on its backside (side opposite to the pressure-sensitive adhesive layer). The backing layer may be formed through a release treatment and/or an antifouling treatment typically with a release agent such as a silicone, a fluorine-containing compound, a long-chain alkyl, or a fatty acid amide; or a silica powder. Above all, the pressure-sensitive adhesive sheet preferably has a structure of [(pressure-sensitive adhesive layer)/(substrate)/(backing layer)].
The pressure-sensitive adhesive sheet according to the present invention preferably has undergone an antistatic treatment. The antistatic treatment may be performed by a common antistatic treatment process, is not limited, but may be performed typically by a process of providing an antistatic layer on the backside (side opposite to the pressure-sensitive adhesive layer) of the substrate, or a process of incorporating a kneading-type antistatic agent (electrification preventing agent) into the substrate.
The antistatic layer may be provided typically by applying an antistatic resin containing an antistatic agent alone or in combination with a resin component, applying an electroconductive resin composition containing an electroconductive material and a resin component, or applying an electroconductive polymer; or by performing vapor deposition or plating of an electroconductive material.
The antistatic agent is exemplified by cationic antistatic agents having a cationic functional group (e.g., a primary, secondary, or tertiary amino group), such as quaternary ammonium salts and pyridinium salts; anionic antistatic agents having an anionic functional group, such as sulfonic acid salts, sulfuric ester salts, phosphoric acid salts, and phosphoric ester salts; amphoteric antistatic agents such as alkylbetaines and derivatives thereof, imidazoline and derivatives thereof, and alanine and derivatives thereof; nonionic antistatic agents such as amino-alcohols and derivatives thereof, glycerol and derivatives thereof, and polyethylene glycols and derivatives thereof; as well as ionic conductive polymers obtained by polymerization or copolymerization of a monomer or monomers having an ionic conductive group, as typified by the cationic antistatic agents, anionic antistatic agents, and amphoteric antistatic agents.
Specifically, the cationic antistatic agents are exemplified by alkyltrimethylammonium salts; acyloylamidopropyltrimethylammonium methosulfates; alkylbenzylmethylammonium salts; acylcholine chlorides; (meth)acrylate copolymers having quaternary ammonium groups, such as poly(dimethylaminoethyl methacrylate)s; styrenic copolymers having quaternary ammonium groups, such as poly(vinylbenzyltrimethylammonium chloride)s; and diallylamine copolymers having quaternary ammonium groups, such as poly(diallyldimethylammonium chloride)s. The anionic antistatic agents are typified by alkylsulfonic acid salts, alkylbenzenesulfonic acid salts, alkyl sulfate salts, alkyl ethoxysulfate salts, alkyl phosphate salts, and sulfo-containing styrenic copolymers. The amphoteric antistatic agents are typified by alkylbetaines, alkylimidazolium betaines, and carbobetaine graft copolymers. The nonionic antistatic agents are exemplified by fatty acid alkylolamides, di-(2-hydroxyethyl)alkylamines, polyoxyethylene alkylamines, fatty acid glycerol esters, polyoxyethylene glycol fatty acid esters, sorbitan fatty acid esters, polyoxysorbitan fatty acid esters, polyoxyethylene alkyl phenyl ethers, polyoxyethylene alkyl ethers, polyethylene glycols, polyoxyethylenediamines, copolymers formed from a polyether, a polyester, and a polyamide, and methoxypolyethylene glycol(meth)acrylates.
The electroconductive polymer is typified by polyanilines, polypyrroles, and polythiophenes.
The electroconductive material is typified by tin oxide, antimony oxide, indium oxide, cadmium oxide, titanium oxide, zinc oxide, indium, tin, antimony, gold, silver, copper, aluminum, nickel, chromium, titanium, iron, cobalt, copper iodide, and alloys or mixtures of them.
The resin component may be any of general-purpose resins such as polyesters, acrylic resins, vinyl polymers, urethane resins, melamine resins, and epoxy resins. The antistatic resin, when containing a polymeric antistatic agent as the antistatic agent, does not have to further contain the resin component. The antistatic resin may further contain, as a crosslinking agent, a compound such as methylolated or alkylolated melamine, urea, glyoxal, or acrylamide compound, as well as an epoxy compound or an isocyanate compound.
The antistatic layer, when to be formed by coating, may be formed by diluting the antistatic resin, the electroconductive polymer, or the electroconductive resin composition with a solvent or dispersion medium (e.g., an organic solvent or water) to give a coating composition, applying the coating composition to the substrate, and drying the applied composition. The organic solvent is exemplified by methyl ethyl ketone, acetone, ethyl acetate, tetrahydrofuran, dioxane, cyclohexanone, n-hexane, toluene, xylene, methanol, ethanol, n-propanol, and isopropyl alcohol. Each of these may be used alone or in combination. The coating may be performed according to a known coating procedure such as roll coating, gravure coating, reverse coating, roll brush coating, spray coating, air knife coating, impregnation, or curtain coating.
The antistatic layer formed by coating (antistatic resin layer, electroconductive polymer layer, or electroconductive resin composition layer) has a thickness of preferably from 0.001 to 5 μm, and more preferably from 0.005 to 1 μm.
Exemplary procedures for the vapor deposition or plating of the electroconductive material include vacuum deposition, sputtering, ion plating, chemical vapor deposition, spray pyrolysis, chemical plating, and electroplating.
The antistatic layer formed by vapor deposition or plating (electroconductive material layer) has a thickness of preferably from 20 to 10000 angstroms, and more preferably from 50 to 5000 angstroms.
Any of the antistatic agents may be suitably used as the kneading-type antistatic agent. The kneading-type antistatic agent may be contained in an amount of preferably 20 percent by weight or less, and more preferably from 0.05 to 10 percent by weight, based on the total weight (100 percent by weight) of the substrate. The way to incorporate the kneading-type antistatic agent into the substrate is not limited, as long as the kneading-type antistatic agent can be uniformly mixed with, for example, a resin for constituting a plastic substrate, and is generally exemplified by a process using a heating roll, Banbury mixer, press kneader, or double-screw kneader.
The pressure-sensitive adhesive composition according to the present invention is a pressure-sensitive adhesive composition capable of forming a pressure-sensitive adhesive layer having excellent adhesiveness and satisfactory removability (easy peelability) and being removable. The composition is therefore used for the formation of a removable pressure-sensitive adhesive layer that is used in applications where the pressure-sensitive adhesive layer will be removed. Specifically, the pressure-sensitive adhesive sheet having a pressure-sensitive adhesive layer formed from the pressure-sensitive adhesive composition according to the present invention may be used in applications where the sheet will be removed. Exemplary applications include masking tapes such as masking tapes for protection or curing in construction, masking tapes for automobile painting, masking tapes for electronic components (e.g., lead frames and printed circuit boards), and masking tapes for sand blasting; surface-protecting films such as surface-protecting films for aluminum sash, surface-protecting films for optical plastics, surface-protecting films for optical glass, surface-protecting films for automobiles, and surface-protecting films for metal plates; pressure-sensitive adhesive tapes for production processes of semiconductor/electronic components, such as backgrinding tapes, pellicle-fixing tapes, dicing tapes, lead-frame-fixing tapes, cleaning tapes, dedusting tapes, carrier tapes, and cover tapes; packaging tapes for electronic appliances and electronic components; temporal tacking tapes used upon transportation; binding tapes; and labels.
The pressure-sensitive adhesive sheet according to the present invention also less suffers from appearance defects such as “dimples” in the pressure-sensitive adhesive layer and has a good appearance. The pressure-sensitive adhesive sheet, when used as being affixed to an adherend, does not cause stains, such as whitening, on the adherend and satisfactorily less causes staining. For these reasons, the pressure-sensitive adhesive sheet according to the present invention is preferably used particularly for the surface protection of optical members (e.g., optical plastics, optical glass, and optical films), typically as a surface-protecting film for an optical member. This is because pressure-sensitive adhesive sheets for use in such optical members should have good appearances and should cause less staining. Exemplary optical members include polarizing plates, retardation films, anti-reflective films, wave plates, compensation films, and brightness enhancing films for constituting panels typically of liquid crystal displays, organic electroluminescence (organic EL) displays, and field emission displays. However, the pressure-sensitive adhesive sheet can also be used for other applications not limited to the above ones and can be used typically for surface-protection, failure-prevention, removal of foreign matter, or masking upon production of microfabricated components of semiconductors (semiconductor devices), circuits, printed circuit boards, masks, and lead frames.
The present invention will be illustrated in further detail with reference to several working examples below. It should be noted, however, that these examples are never construed to limit the scope of the present invention. All parts and percentages below are by weight, unless otherwise specified.
In a vessel were placed 90 parts by weight of water, as well as constitutive monomers and an emulsifier in amounts given in Table 1, and they were mixed with stirring using a homomixer to yield a monomer emulsion.
Next, 50 parts by weight of water, 0.01 part by weight of a polymerization initiator (ammonium persulfate), and the above-prepared monomer emulsion in an amount corresponding to 10 percent by weight thereof were placed in a reactor equipped with a condenser, a nitrogen inlet tube, a thermometer, and a stirrer, followed by emulsion polymerization with stirring at 65° C. for one hour. Another portion (0.05 part by weight) of the polymerization initiator (ammonium persulfate) was further added and, to the stirred mixture, all the residual monomer emulsion (in an amount corresponding to 90 percent by weight) was added over 3 hours, followed by a reaction at 75° C. for 3 hours. This was cooled to 30° C., combined with a 10 percent by weight ammonia water to be adjusted to pH 8, and thereby yielded a water dispersion of acrylic emulsion polymer having a concentration of the acrylic emulsion polymer of 42 percent by weight.
To 238 parts by weight of the above-prepared water dispersion of acrylic emulsion polymer (42 percent by weight) (i.e., to 100 parts by weight of the acrylic emulsion polymer) were added 3 parts by weight of an epoxy crosslinking agent [trade name “TETRAD-C” supplied by Mitsubishi Gas Chemical Company, Inc., 1,3-bis(N,N-diglycidylaminomethyl)cyclohexane, having an epoxy equivalent of 110 and a number of functional groups of 4] as a water-insoluble crosslinking agent, 1 part by weight (0.75 part by weight as active acetylenic diol compound) of an acetylenic diol compound (composition) having an HLB of 4 [trade name “SURFYNOL 104H” supplied by Air Products and Chemicals Inc., containing 75 percent by weight active ingredient], and 0.1 part by weight of a polypropylene glycol [trade name “Polypropylene Glycol, Diol Type” supplied by Wako Pure Chemical Industries, Ltd., having a number-average molecular weight Mn of 3000 and a PO content of 100 percent by weight] were added and mixed by stirring at 300 rpm with a stirrer at 23° C. for 10 minutes, and thereby yielded a removable water-dispersible acrylic pressure-sensitive adhesive composition.
The above-prepared removable water-dispersible acrylic pressure-sensitive adhesive composition was applied to a corona-treated surface of a PET film (trade name “T100N38” supplied by Mitsubishi Plastics, Inc., having a thickness of 38 μm) using an applicator supplied by Tester Sangyo Co., Ltd., so as to have a dry thickness of 15 μm, dried in an oven with internal air circulation at 120° C. for 2 minutes, further aged at 50° C. for 3 days, and thereby yielded a pressure-sensitive adhesive sheet.
Removable water-dispersible acrylic pressure-sensitive adhesive compositions and pressure-sensitive adhesive sheets were prepared by the procedure of Example 1, except for using a polyether defoaming agent of a different type as indicated in Table 1.
Removable water-dispersible acrylic pressure-sensitive adhesive compositions and pressure-sensitive adhesive sheets were prepared by the procedure of Example 1, except for using an acetylenic diol compound of a different type and/or a defoaming agent of a different type, as indicated in Table 1.
A monomer emulsion was prepared by the procedure of Example 1, except for using constitutive monomers of different types and/or in different amounts as indicated in Table 1.
Except for using this monomer emulsion, a removable water-dispersible acrylic pressure-sensitive adhesive composition and a pressure-sensitive adhesive sheet were prepared by the procedure of Example 1.
A monomer emulsion was prepared by the procedure of Example 1, except for using constitutive monomers of different types and/or in different amounts as indicated in Table 1.
A removable water-dispersible acrylic pressure-sensitive adhesive composition and a pressure-sensitive adhesive sheet were prepared by the procedure of Example 1, except for using the above-prepared monomer emulsion, using the water-insoluble crosslinking agent in a different amount, and further using a hydrazide crosslinking agent.
Removable water-dispersible acrylic pressure-sensitive adhesive compositions and pressure-sensitive adhesive sheets were prepared by the procedure of Example 1, except for using no polyether defoaming agent as indicated in Table 1. Comparative Example 3 employed a silicone defoaming agent.
A removable water-dispersible acrylic pressure-sensitive adhesive composition and a pressure-sensitive adhesive sheet were prepared by the procedure of Example 1, except for using no acetylenic diol compound as indicate in Table 1.
A removable water-dispersible acrylic pressure-sensitive adhesive composition and a pressure-sensitive adhesive sheet were prepared by the procedure of Example 1, except for using not a water-insoluble crosslinking agent but a water-soluble crosslinking agent alone as a crosslinking agent.
The pressure-sensitive adhesive sheets obtained in the examples and comparative examples were evaluated according to the following measurement or evaluation methods. The solvent-insoluble content of the pressure-sensitive adhesive layer (after crosslinking) was measured according to the aforementioned measurement method.
The evaluation results are indicated in Table 1.
Each of the pressure-sensitive adhesive sheets obtained in the examples and comparative examples (sample size: 25 mm wide by 100 mm long) was affixed to a polarizing plate (trade name “SEG1425DUHC” supplied by Nitto Denko Corporation, 70 mm wide by 120 mm long) using a laminator (tabletop laminator, supplied by Tester Sangyo Co., Ltd.) at a pressure (load) of 0.25 MPa and a rate of 0.3 m/min.
The polarizing plate with the pressure-sensitive adhesive sheet being affixed thereto was as intact left stand at 80° C. for 4 hours, followed by removal of the pressure-sensitive adhesive sheet therefrom. The polarizing plate, from which the pressure-sensitive adhesive sheet had been removed, was left stand in a high-humidity environment (at 23° C. and 90% relative humidity) for 12 hours, the surface of which was visually observed, and whether and how the polarizing plate was stained was evaluated according to the following criteria:
Less staining (Good): No change was observed in a region where the pressure-sensitive adhesive sheet had been affixed, as compared to a region where the pressure-sensitive adhesive sheet had not been affixed.
Staining (Poor): Whitening was observed in the region where the pressure-sensitive adhesive sheet had been affixed.
Each of the pressure-sensitive adhesive sheets obtained in the examples and comparative examples (sample size: 25 mm wide by 100 mm long) was affixed to a polarizing plate at a pressure (load) of 0.25 MPa and a rate of 0.3 m/min using a laminator (tabletop laminator, supplied by Tester Sangyo Co., Ltd.) to give a laminated sample. The polarizing plate is made from a triacetyl cellulose (TAC) and has an arithmetic mean surface roughness Ra of about 21 nm in the machine direction (MD), about 31 nm in the transverse direction (TD), and about 26 nm on an average of the machine direction and the transverse direction.
The laminated sample of the pressure-sensitive adhesive sheet and the polarizing plate was left stand in an environment of 23° C. and 50% relative humidity for 20 minutes, subjected to a 180-degree peel test under conditions mentioned later to measure an adhesive strength (N/25 mm) of the pressure-sensitive adhesive sheet to the polarizing plate, and the measured adhesive strength was defined as an “initial adhesive strength.”
(Adhesive Strength after Affixation/Storage at 40° C. for One Week)
Each of the pressure-sensitive adhesive sheets obtained in the examples and comparative examples (sample size: 25 mm wide by 100 mm long) was affixed to a polarizing plate using a laminator (tabletop laminator, supplied by Tester Sangyo Co., Ltd.) at a pressure (load) of 0.25 MPa and a rate of 0.3 m/min to give a laminated sample. The polarizing plate is made from a triacetyl cellulose (TAC) and has an arithmetic mean surface roughness Ra of about 21 nm in the machine direction, about 31 nm in the transverse direction, and about 26 nm on average in the machine direction and the transverse direction.
The laminated sample of the pressure-sensitive adhesive sheet and the polarizing plate was stored in an environment of 40° C. for one week, left stand in an environment of 23° C. and 50% relative humidity for 2 hours, subjected to a 180-degree peel test under the following conditions to measure an adhesive strength (N/25 mm) of the pressure-sensitive adhesive sheet to the polarizing plate, and the measured adhesive strength was defined as an “adhesive strength after affixation/storage at 40° C. for one week.”
The 180-degree peel test was performed using a tensile tester in an environment of 23° C. and 50% relative humidity at a tensile speed of 0.3 m/min.
A sample may be evaluated as having excellent resistance to increase in adhesive strength, when having a difference between the initial adhesive strength and the adhesive strength after affixation/storage at 40° C. for one week [(adhesive strength after affixation/storage at 40° C. for one week)-(initial adhesive strength)] of 0.10 N/25 mm or less.
The surface of the pressure-sensitive adhesive layer of each of the pressure-sensitive adhesive sheets obtained in the examples and comparative examples was visually observed, by which a number of defects (dimples and bubbles) in an observation area of 10 cm wide and 10 cm long was counted, and the appearance was evaluated according to the following criteria:
Good appearance (Good): The sample had a number of defects of from 0 to 100; and
Poor appearance (Poor): The sample had a number of defects of 101 or more.
(4) Elongation at Break (Elongation at Rupture) of Pressure-Sensitive Adhesive Layer (after Crosslinking) [Tensile Test]
Each of the removable water-dispersible acrylic pressure-sensitive adhesive compositions prepared in the examples and comparative examples was applied to a surface, which had been treated with a silicone, of a PET film (“MRF38” supplied by Mitsubishi Plastics, Inc.) so as to have a dry thickness of 50 μm, dried in an oven with internal air circulation at 120° C. for 2 minutes, aged at 50° C. for 3 days, and thereby yielded a pressure-sensitive adhesive layer.
Next, the pressure-sensitive adhesive layer was rounded to give a cylindrical pressure-sensitive adhesive layer sample (50 mm in length and 1 mm2 in sectional area (base area)).
The elongation at rupture (elongation at break) was measured by performing a tensile test at a tensile speed of 50 mm/min using a tensile tester, while setting chucks so as to give an initial measurement length (chuck-to-chuck distance) of 10 mm.
The elongation at rupture (elongation at break) indicates a percentage elongation at the time when the specimen (pressure-sensitive adhesive layer sample) breaks in the tensile test, and is calculated according to the following expression:
Elongation at rupture (elongation at break) (%)=[(Length of specimen at break (chuck-to-chuck distance at break))−(Initial length (10 mm))]/(Initial length (10 mm))×100
Abbreviations used in Table 1 are as follows. The amounts of the respective components of the removable water-dispersible acrylic pressure-sensitive adhesive compositions in Table 1 are indicated as actual blending amounts (blending amounts of the commercial products). The amount of the acrylic emulsion polymer (A) is indicated as the weight of solid matter (solids content).
2EHA: 2-Ethylhexyl acrylate
DAAM: Diacetoneacrylamide
MMA: Methyl methacrylate
AA: Acrylic acid
SE-10N: Trade name “ADEKA REASOAP SE-10N” (nonionic-anionic reactive emulsifier) supplied by ADEKA CORPORATION
TETRAD-C: Trade name “TETRAD-C” (1,3-bis(N,N-diglycidylaminomethyl)cyclohexane, having an epoxy equivalent of 110 and a number of functional groups of 4) supplied by Mitsubishi Gas Chemical Company, Inc.
Adipic acid dihydrazide: Trade name “Adipic Acid Dihydrazide” supplied by Tokyo Chemical Industry Co., Ltd.
DENACOL EX-512: Trade name “DENACOL EX-512” (polyglycerol polyglycidyl ether, having an epoxy equivalent of 168 and a number of functional groups of about 4) supplied by Nagase ChemteX Corporation
SURFYNOL 104H: Trade name “SURFYNOL 104H” (having an HLB of 4 and containing 75 percent by weight active ingredient) supplied by Air Products and Chemicals Inc.
SURFYNOL 104PG-50: Trade name “SURFYNOL 104PG-50” (having an HLB of 4 and containing 50 percent by weight active ingredient) supplied by Air Products and Chemicals Inc.
SURFYNOL 420: Trade name “SURFYNOL 420” (having an HLB of 4 and containing 100 percent by weight active ingredient) supplied by Air Products and Chemicals Inc.
SURFYNOL 440: Trade name “SURFYNOL 440” (having an HLB of 8 and containing 100 percent by weight active ingredient) supplied by Air Products and Chemicals Inc.
SURFYNOL 465: Trade name “SURFYNOL 465” (having an HLB of 13 and containing 100 percent by weight active ingredient) supplied by Air Products and Chemicals Inc.
Polypropylene glycol: Trade name “Polypropylene Glycol, Diol Type” (having a number-average molecular weight of 3000 and a PO content of 100 percent by weight, and containing 100 percent by weight active ingredient) supplied by Wako Pure Chemical Industries, Ltd.
ADEKA PLURONIC L-61: Trade name “ADEKA PLURONIC L-61” (having a number-average molecular weight of 2000 and a PO content of 90 percent by weight, and containing 100 percent by weight active ingredient) supplied by ADEKA CORPORATION
ADEKA PLURONIC 25R-1: Trade name “ADEKA PLURONIC 25R-1” (having a number-average molecular weight of 2800 and a PO content of 90 percent by weight, and containing 100 percent by weight active ingredient) supplied by ADEKA CORPORATION
ADEKA PLURONIC 25R-2: Trade name “ADEKA PLURONIC 25R-2” (having a number-average molecular weight of 3100 and a PO content of 80 percent by weight, and containing 100 percent by weight active ingredient) supplied by ADEKA CORPORATION
ADEKA PLURONIC 17R-3: Trade name “ADEKA PLURONIC 17R-3” (having a number-average molecular weight of 2000 and a PO content of 70 percent by weight, and containing 100 percent by weight active ingredient) supplied by ADEKA CORPORATION
ADEKA PLURONIC P-65: Trade name “ADEKA PLURONIC P-65” (having a number-average molecular weight of 3500 and a PO content of 50 percent by weight, and containing 100 percent by weight active ingredient) supplied by ADEKA CORPORATION
ADEKA PLURONIC L-31: Trade name “ADEKA PLURONIC L-31” (having a number-average molecular weight of 1100 and a PO content of 90 percent by weight, and containing 100 percent by weight active ingredient) supplied by ADEKA CORPORATION
ADEKA PLURONIC L-121: Trade name “ADEKA PLURONIC L-121” (having a number-average molecular weight of 4500 and a PO content of 90 percent by weight, and containing 100 percent by weight active ingredient) supplied by ADEKA CORPORATION
SN-DEFOAMER 1315: Trade name “SN-DEFOAMER 1315” (silicone defoaming agent) supplied by SAN NOPCO LIMITED
The results in Table 1 demonstrate as follows. The pressure-sensitive adhesive sheets (Examples 1 to 10) each having a pressure-sensitive adhesive layer formed from a pressure-sensitive adhesive composition satisfying the conditions specified in the present invention had good appearances and did not cause whitening as stains on the polarizing plates even in a high-humidity environment after they were affixed to and removed from the polarizing plates, thus satisfactorily less causing staining. They also had small increases in adhesive strength with time after the affixation.
By contrast, the sample using no polyether defoaming agent (Comparative Example 1) suffered from bubble defects in the pressure-sensitive adhesive layer; the sample using no acetylenic diol compound (Comparative Example 2) suffered from dimple defects in the pressure-sensitive adhesive layer; and the sample using a silicone defoaming agent (Comparative Example 3) suffered from dimple defects in the pressure-sensitive adhesive layer, thus each having poor appearances. The sample using an acetylenic diol compound having an HLB of 13 or more (Comparative Example 4), the sample using a polyether defoaming agent having a PO content of less than 70 percent by weight (Comparative Example 5), and the samples using polyether deforming agents having a PO content of less than 1200 or more than 4000 (Comparative Examples 6 and 7) caused whitening as stains on the adherend in a high-humidity environment. The sample using no water-insoluble crosslinking agent (Comparative Example 8) had high adhesive strengths after affixation/storage and suffered from large increases in adhesive strength with time.
As is described above, the samples using the pressure-sensitive adhesive compositions not satisfying the conditions specified in the present invention failed to balance a good appearance, less-causing properties, and satisfactory resistance to increase in adhesive strength.
Pressure-sensitive adhesive compositions according to embodiments of the present invention give pressure-sensitive adhesive layers and, in turn, pressure-sensitive adhesive sheets having the pressure-sensitive adhesive layers, which have excellent removability, satisfactory adhesiveness, and good appearances, cause (leave) substantially no stain on the surface of an adherend after removal, and thus less cause staining. In addition, the pressure-sensitive adhesive layers (pressure-sensitive adhesive sheets) are resistant to increase in adhesive strength to the adherend with time. For these reasons, the pressure-sensitive adhesive compositions according to the present invention are useful as pressure-sensitive adhesive compositions for the formation of pressure-sensitive adhesive layers of pressure-sensitive adhesive sheets which are used for surface protection of optical films.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2010-097232 | Apr 2010 | JP | national |
| 2010-097233 | Apr 2010 | JP | national |
| 2010-097234 | Apr 2010 | JP | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/JP2011/059075 | 4/12/2011 | WO | 00 | 10/15/2012 |
