Patent Application
20140256877
1. Technical Field
The present invention relates to a pressure-sensitive adhesive sheet.
2. Background Art
Recently, in various fields, display devices such as a liquid crystal display (LCD), or input devices which are used in combination with the display devices, such as touch panels, have been widely used. In the production or the like of those display devices or input devices, transparent pressure-sensitive adhesive sheets have been used for the purpose of laminating optical members. For instance, transparent pressure-sensitive adhesive sheets have been used for laminating touch panels, lenses or the like to display devices (such as LCDs) (see e.g. Patent Documents 1 to 3).
Patent Document 1: JP-A-2003-238915
Patent Document 2: JP-A-2003-342542
Patent Document 3: JP-A-2004-231723
The pressure-sensitive adhesive sheet to be used for the above use has been required to be excellent in the property of being able to exhibit the pressure-sensitive adhesive force (pressure-sensitive adhesive property) even at −30° C., in order for members laminated by the pressure-sensitive adhesive sheet not to peel away during the use at not only about room temperature (23° C.) but also even a low temperature on the order of −30° C. In addition, recently, there has been a growing need for removal (rework) (especially removal at a low temperature) in the case where the optical members are bonded together, and then, they are required to be bonded again or the like. In particular, there have been growing needs for pressure-sensitive adhesive sheets which have excellent pressure-sensitive adhesiveness even at a temperature on the order of −30° C. and can be removed at a temperature less than −30° C., such as a temperature on the order of −50° C. or less.
However, conventional pressure-sensitive adhesive sheets capable of being removed are excellent in pressure-sensitive adhesive properties at about room temperature (23° C.), but there have been cases where the pressure-sensitive adhesive force thereof has been reduced at a temperature on the order of −30° C. and the conventional pressure-sensitive adhesive sheets have been separated from adherends. More specifically, it is the status quo that pressure-sensitive adhesive sheets, which have excellent pressure-sensitive adhesive properties in a wide temperature range of about −30° C. to room temperature (23° C.) and can be removed (having reworkability) at a low temperature on the order of −50° C. or less, are still unknown.
Additionally, the pressure-sensitive adhesive properties in a wide temperature range of about −30° C. to room temperature (23° C.) and the reworkability at a temperature on the order of −50° C. or less are required in not only the use for lamination of optical members but also various uses.
An object of the present invention is therefore to provide a pressure-sensitive adhesive sheet containing a pressure-sensitive adhesive layer which is excellent in the pressure-sensitive adhesive properties in a temperature range of about −30° C. to room temperature (23° C.) and has the reworkability at a temperature on the order of −50° C. or less.
As a result of extensive studies by the present inventors, the present inventors have found that the pressure-sensitive adhesive sheet containing a pressure-sensitive adhesive layer having a melting point of the specific range is excellent in the pressure-sensitive adhesive properties in a temperature range of about −30° C. to room temperature (23° C.) and has the reworkability at a temperature on the order of −50° C. or less, and thus, the present invention has been accomplished.
That is, the present invention provides the pressure-sensitive adhesive sheet, comprising a pressure-sensitive adhesive layer having a melting point of −60° C. to 0° C.
Because the pressure-sensitive adhesive sheet of the present invention has the above constitution, the present pressure-sensitive adhesive sheet is excellent in the pressure-sensitive adhesive properties in a temperature range of about −30° C. to room temperature (23° C.) and has the reworkability at a temperature on the order of −50° C. or less.
The pressure-sensitive adhesive sheet of the present invention contains at least one layer of a pressure-sensitive adhesive layer having a melting point of −60° C. to 0° C. (which is referred to as the “pressure-sensitive adhesive layer of the present invention” in some cases). The pressure-sensitive adhesive layer of the present invention may contain a substrate, a pressure-sensitive adhesive layer (other pressure-sensitive adhesive layer) other than the pressure-sensitive adhesive layer of the present invention and the other layer (for example, an intermediate layer, undercoating layer and the like) within the range of not impairing the effects of the present invention. With regard to the layer other than the pressure-sensitive adhesive layer of the present invention, only one layer thereof may be contained, and two or more layers thereof may be contained, respectively. The term “pressure-sensitive adhesive sheet” includes the meaning of a “pressure-sensitive adhesive tape”. That is, the pressure-sensitive adhesive sheet of the present invention may be a pressure-sensitive adhesive tape in a tape form.
The pressure-sensitive adhesive sheet of the present invention may be a single-sided pressure-sensitive adhesive sheet which has the surface of a pressure-sensitive adhesive layer (pressure-sensitive adhesive surface) on one side alone, or it may be a double-sided pressure-sensitive adhesive sheet which has the surfaces of a pressure-sensitive adhesive layer on both sides. The pressure-sensitive adhesive sheet of the present invention is not particularly limited, but is preferably a double-sided pressure-sensitive adhesive sheet, more preferably a double-sided pressure-sensitive adhesive sheet having the surfaces of the pressure-sensitive adhesive layer of the present invention on both sides, from the viewpoint of allowing the use for laminating two adherends together.
The pressure-sensitive adhesive sheet of the present invention may be a pressure-sensitive adhesive sheet having no substrate (substrate layer), or the so-called “substrateless-type” pressure-sensitive adhesive sheet (which is referred to as “substrateless pressure-sensitive adhesive sheet in some cases), or it may be a pressure-sensitive adhesive sheet having a substrate. Examples of the substrateless pressure-sensitive adhesive sheet include a double-sided pressure-sensitive adhesive sheet consisting of the pressure-sensitive adhesive layer of the present invention and a double-sided pressure-sensitive adhesive sheet including the pressure-sensitive adhesive layer of the present invention and a pressure-sensitive adhesive layer other than the pressure-sensitive adhesive layer of the present invention (which is referred to as “other pressure-sensitive adhesive layer” in some cases). Examples of the pressure-sensitive adhesive sheet having a substrate include a single-sided pressure-sensitive adhesive sheet having the pressure-sensitive adhesive layer of the present invention on one side of the substrate thereof, a double-sided pressure-sensitive adhesive sheet having the pressure-sensitive adhesive layer of the present invention on both sides of the substrate thereof, and a double-sided pressure-sensitive adhesive sheet having the pressure-sensitive adhesive layer of the present invention on one side of the substrate thereof and the other pressure-sensitive adhesive layer on the other side of the substrate thereof.
Of these, from the viewpoint of improvements in optical properties such as transparency, the substrateless pressure-sensitive adhesive sheets are preferred and the double-sided substrateless pressure-sensitive adhesive sheet consisting of the pressure-sensitive adhesive layer of the present invention is more preferred. If the pressure-sensitive adhesive sheet of the present invention is a pressure-sensitive adhesive sheet having a substrate, there is no particular restriction, but the pressure-sensitive adhesive sheet of the present invention is preferably a double-sided pressure-sensitive adhesive sheet having the pressure-sensitive adhesive layer of the present invention on both sides of the substrate in terms of workability. The term “substrate (substrate layer)” used herein refers to the part to be laminated to an adherend together with the pressure-sensitive adhesive layer when the pressure-sensitive adhesive sheet of the present invention is applied (laminated) to the adherend (e.g. an optical member), and does not include a separator (release liner) to be peeled away when the pressure-sensitive adhesive sheet is used (laminated).
The pressure-sensitive adhesive layer of the present invention is preferably formed from a pressure-sensitive adhesive composition containing an acrylic polymer produced by polymerizing a monomer component(s) or a partial polymerization product of the monomer component(s).
The pressure-sensitive adhesive composition to form the pressure-sensitive adhesive sheet of the present invention preferably contains an acrylic polymer produced by polymerizing a monomer component(s) or a partial polymerization product of the monomer component(s). The pressure-sensitive adhesive composition may further contain a polymerization initiator, a silane coupling agent, an oligomer, a cross-linking agent, a solvent and an additive.
Examples of the pressure-sensitive adhesive composition containing a partial polymerization product of the monomer component(s) include a so-called active energy-ray curable pressure-sensitive adhesive composition. Examples of the pressure-sensitive adhesive composition containing an acrylic polymer produced by polymerizing the monomer component(s) include a so-called solvent type pressure-sensitive adhesive composition.
The term “partial polymerization product of the monomer component(s)” means a material obtained by partially polymerizing one or two or more of the monomer component(s). More specifically, examples thereof include a mixture of the monomer component(s) with a partial polymerization product of the monomer component(s).
The monomer component to constitute (form) the acrylic polymer preferably include alkyl (meth)acrylate having an alkyl group having 10 to 13 carbon atoms (which is referred to as “C10-13 alkyl (meth)acrylate” in some cases) and a polar group-containing monomer other than a carboxyl group-containing monomer (which is referred simply to as “a polar group-containing monomer” hereafter in some cases). In other words, the acrylic polymer preferably contains, as essential monomer components, C10-13 alkyl (meth)acrylate and the polar group-containing monomer other than the carboxyl group-containing monomer.
The term “(meth)acryl” means “acryl” and/or “methacryl” (either of “acryl” or “methacryl”, or both of them), and hereafter the same meaning is given thereto. In addition, the term “alkyl group” means a straight- or branched-chain alkyl group unless otherwise specified.
The term “polar group-containing monomer” in this specification means, unless otherwise indicated, a polar group-containing monomer other than a carboxyl group-containing monomer (a monomer containing, in a molecular thereof, a polar group other than a carboxyl group).
The C10-13 alkyl (meth)acrylate is not particularly limited, and examples thereof include decyl (meth)acrylate, isodecyl (meth)acrylate, undecyl (meth)acrylate, dodecyl (meth)acrylate, tridecyl (meth)acrylate and the like. Of these (meth)acrylates, dodecyl acrylate (lauryl acrylate) is preferred. The C10-13 alkyl (meth)acrylates as recited above may be used alone, or in combination of two or more thereof.
If the polar group-containing monomer as defined above is included in the monomer component, since the polar group-containing monomer has moderate polarity, a pressure-sensitive adhesive layer formed from the pressure-sensitive adhesive composition can develop moderate pressure-sensitive adhesive force.
The polar group-containing monomer is not particularly limited and is preferably an ethylenically unsaturated monomer containing a polar group, and examples thereof include hydroxyl group-containing monomers such as hydroxyalkyl (meth)acrylate such as 2-hydroxyethyl (meth)acrylate, 3-hydroxypropyl (meth)acrylate, 4-hydroxybutyl (meth)acrylate and 6-hydroxyhexyl (meth)acrylate, vinyl alcohol and allyl alcohol; amide group-containing monomers such as (meth)acrylamide, N,N-dimethyl (meth) acrylamide, N-methylol (meth) acrylamide, N-methoxymethyl (meth) acrylamide, N-butoxymethyl (meth)acrylamide, N-hydroxyethyl (meth)acrylamide and N,N-dimethylaminopropyl (meth)acrylamide; amino group-containing monomers such as aminoethyl (meth)acrylate, dimethylaminoethyl (meth)acrylate and t-butylaminoethyl (meth)acrylate; epoxy group-containing monomers such as glycidyl (meth)acrylate and methylglycidyl (meth)acrylate; cyano group-containing monomers such as acrylonitrile and methacrylonitrile; hetero ring-containing vinyl monomers such as N-vinyl-2-pyrrolidone, N-vinylcaprolactam, (meth)acryloyl morpholine, N-vinylpyridine, N-vinylpiperidone, N-vinylpyrimidine, N-vinylpiperazine, N-vinylpyrrole, N-vinylimidazole, and N-vinyloxazole; sulfonic acid group-containing monomers such as sodium vinylsulfonate; phosphoric acid group-containing monomers such as 2-hydroxyethyl acryloyl phosphate; imide group-containing monomers such as cyclohexyl maleimide and isopropyl maleimide; and isocyanate group-containing monomers such as 2-methacryloyloxyethyl isocyanate; and the like. The polar group-containing monomer may be used either alone or in combination of two or more thereof.
The polar group-containing monomers are not particularly limited, but preferably include at least one monomer selected from the group consisting of hydroxyl group-containing monomers and nitrogen atom-containing monomers (one or more kinds of monomers selected from the group consisting of hydroxyl group-containing monomers and nitrogen atom-containing monomers) from the viewpoint of preventing the pressure-sensitive adhesive composition from excessively increasing the pressure-sensitive adhesive force with the lapse of time. Of these, from the viewpoint of developing moderate pressure-sensitive adhesive force and ensuring a moderate elastic modulus at room temperature (excellent step absorbability), it is preferred that the hydroxyl group-containing monomer and the nitrogen atom-containing monomer be both included in the polar group-containing monomers.
The nitrogen atom-containing monomer is a monomer containing at least one nitrogen atom in a molecule thereof. Examples of the nitrogen atom-containing monomer include the above amide group-containing monomers and the hetero ring-containing vinyl monomers containing a nitrogen atom of the above hetero ring-containing vinyl monomers. Of these monomers, N-vinyl-2-pyrrolidone (NVP), N-vinylcaprolactam (NVC) and N,N-dimethylacrylamide (DMAA) are preferred.
From the viewpoint of preventing the pressure-sensitive adhesive composition from excessively increasing the pressure-sensitive adhesive force with the lapse of time and increasing the pressure-sensitive adhesive force with respect to polarizing plates, as the nitrogen atom-containing monomer, preferable examples thereof include nitrogen atom-containing monomers containing a tertiary amino group (tertiary amino group-containing monomers), and particularly preferable examples thereof include dimethylaminopropyl acrylamide (DMAPAA) and dimethylamino ethylacrylate (DMAEA).
The hydroxyl group-containing monomer is not particularly limited and preferable examples thereof include 2-hydroxyethyl acrylate.
The monomer component may further include an alicyclic monomer. In other words, the monomer component may include an alicyclic monomer as needed basis. The alicyclic monomer is an alicyclic compound excluding an aromatic compound, and is a monomer containing a non-aromatic ring in a molecule thereof. Examples of the non-aromatic ring include non-aromatic alicyclic rings (for example, cycloalkane rings such as a cyclopentane ring, a cyclohexane ring, a cycloheptane ring and a cyclooctane ring, and cycloalkene rings such as a cyclohexene ring) and non-aromatic crosslinking rings (for example, bicyclic hydrocarbon rings such as pinane, pinene, bornane, norbornane and norbornene, tricyclic hydrocarbon rings such as adamantane, and other crosslinking hydrocarbon rings such as tetracyclic hydrocarbon rings).
The alicyclic monomer is not particularly limited, and examples thereof include cycloalkyl (meth)acrylate such as cyclopentyl (meth)acrylate, cyclohexyl (meth)acrylate, cycloheptyl (meth)acrylate and cyclooctyl (meth)acrylate; (meth)acrylic acid esters having bicyclic hydrocarbon rings, such as bornyl (meth)acrylate, isobornyl (meth)acrylate, dicyclopentanyl (meth)acrylate and dicyclopentanyloxyethyl (meth)acrylate; and (meth)acrylic acid esters having tri- or multi-cyclic hydrocarbon rings, such as tricyclopentanyl (meth)acrylate, 1-adamantyl (meth)acrylate, 2-methyl-2-adamantyl (meth)acrylate and 2-ethyl-2-adamantyl (meth)acrylate. Of these alicyclic monomers, cyclohexyl acrylate (CHA), cyclohexyl methacrylate (CHMA), isobornyl acrylate (IBXA) and isobornyl methacrylate (IBXMA) are preferred. The alicyclic monomers as recited above may be used alone or in combination of two or more thereof.
From the viewpoint of developing moderate pressure-sensitive adhesive force at room temperature and ensuring excellent reworkability at a temperature on the order of −50° C. or less, it is preferable that the monomer component include the polar group-containing monomer and the alicyclic monomer.
In the case where an adherend contain a metal or metal oxide (e.g. a transparent conductive coating of a transparent conductive film such as an ITO film), it is preferred that carboxyl group-containing monomers are not substantially contained from the standpoints that the adherend hardly suffer from corrosion, the property of filling up a step difference, such as a printing step difference, at room temperature (step absorbability) can be further enhanced and an increase of the pressure-sensitive adhesive force with the lapse of time is hard to occur. The expression “not substantially contained” means that active incorporation is not carried out, except unavoidable incorporation. More specifically, the content of the carboxyl group-containing monomers in the monomer component(s) is preferably less than 0.05 wt %, more preferably less than 0.01 wt %, further more preferably less than 0.001 wt %, with respect to the total amount (100 wt %) of the monomer component(s). Examples of the carboxyl group-containing monomer include acrylic acid (AA), methacrylic acid, itaconic acid, maleic acid, fumaric acid and crotonic acid. Additionally, acid anhydrides of these carboxyl group-containing monomers (e.g. acid anhydride-containing monomers, such as maleic anhydride and itaconic anhydride) are also included in the carboxyl group-containing monomers.
The monomer component may further include a polyphunctional monomer. The polyfunctional monomer is not particularly limited, and examples thereof include hexanediol di(meth)acrylate (e.g. 1,6-hexanediol di(meth)acrylate), butanediol di(meth)acrylate, (poly)ethylene glycol di(meth)acrylate, (poly)propylene glycol di(meth)acrylate, neopentyl glycol di(meth)acrylate, pentaerythritol di(meth)acrylate (tetramethylolmethane tri(meth)acrylate), pentaerythritol tri(meth)acrylate, dipentaerythritol hexa(meth)acrylate, trimethylolpropane tri(meth)acrylate, allyl (meth)acrylate, vinyl (meth)acrylate, divinylbenzene, epoxyacrylate, polyester acrylate and urethane acrylate. Among these, 1,6-hexanediol diacrylate (HDDA) and dipentaerythritol hexaacrylate (DPHA) are preferred. The polyfunctional monomer may be used alone or in combination of two or more thereof.
The monomer component may further include monomers (other monomers) other than the C10-13 alkyl (meth)acrylate, the polar group-containing monomer, the alicyclic monomer and the polyfunctional monomer.
Examples of other monomers include (meth)acrylic acid ester having aromatic hydrocarbyl groups, such as phenyl (meth)acrylate, phenoxyethyl (meth)acrylate and benzyl (meth)acrylate; alkoxyalkyl (meth)acrylate-based monomer, such as methoxyethyl (meth)acrylate and ethoxyethyl (meth)acrylate; and alkyl (meth)acrylate having an alkyl group having 1 to 9 carbon atoms (referred to as “C1-9 alkyl (meth)acrylate in some cases) and alkyl (meth)acrylate having an alkyl group having 14 to 24 carbon atoms (referred to as “C14-24 alkyl (meth)acrylate in some cases). Further examples thereof include vinyl esters such as vinyl acetate and vinyl propionate; aromatic vinyl compounds such as styrene and vinyl toluene; olefins or dienes, such as ethylene, butadiene, isoprene and isobutylene; vinyl ethers such as vinyl alkyl ethers; and vinyl chloride. The other monomers as recited above can be used alone or in combination of two or more thereof.
The C1-9 alkyl (meth)acrylate is not particularly limited, and examples thereof include methyl (meth)acrylate, ethyl (meth)acrylate, propyl (meth)acrylate, isopropyl (meth)acrylate, n-butyl (meth)acrylate, isobutyl (meth)acrylate, s-butyl (meth)acrylate, t-butyl (meth)acrylate, pentyl (meth)acrylate, isopentyl (meth)acrylate, hexyl (meth)acrylate, heptyl (meth)acrylate, octyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, isooctyl (meth)acrylate, nonyl (meth)acrylate and isononyl (meth)acrylate.
The C14-24 alkyl (meth)acrylate is not particularly limited, and examples thereof include tetradecyl (meth)acrylate, pentadecyl (meth)acrylate, isopentadecyl (meth)acrylate, hexadecyl (meth)acrylate, isohexadecyl (meth)acrylate, heptadecyl (meth)acrylate, isoheptadecyl (meth)acrylate, octadecyl (meth)acrylate, isooctadecyl (meth)acrylate, docosyl (meth)acrylate, isodocosyl (meth)acrylate, tetracosyl (meth)acrylate and isotetracosyl (meth)acrylate.
The content of the C10-13 alkyl (meth)acrylate in the monomer component(s) is not particularly limited, and the content thereof is, for example, 40 wt % or more and less than 80 wt %, preferably from 45% to 78 wt %, further preferably from 50% to 76 wt %, with respect to the total amount (100 wt %) of the monomer component(s). By controlling the content of the C10-13 alkyl (meth)acrylate to 40 wt % or more and less than 80 wt %, the pressure-sensitive adhesive layer containing the resulting acrylic polymer can have still more excellent pressure-sensitive adhesive property even at a low temperature on the order of 30° C. In addition, in such a layer, the pressure-sensitive adhesive force can be reduced at a temperature on the order of −50° C. or less, thereby allowing the removal thereof.
If the C1-9 alkyl (meth)acrylate is included in the monomer component(s), the content thereof is not particularly limited, but is preferably e.g. more than 0 wt % and 40 wt % or less, more preferably from 5% to 30 wt %, further preferably from 10% to 20 wt %, with respect to the total amount (100 wt %) of monomer component(s). By controlling the content of the C1-9 alkyl (meth)acrylate to 40 wt % or less, the pressure-sensitive adhesive layer containing the resulting acrylic polymer can have a more moderate elastic modulus and develop higher pressure-sensitive adhesive force at an ordinary temperature (about 23° C.).
The total content of the polar group-containing monomers and the alicyclic monomers in the monomer component(s) is not particularly limited, and the content thereof is, for example, 15 wt % or more (e.g. from 15% to 50 wt %), preferably from 18% to 40 wt %, more preferably from 20% to 30 wt %, with respect to the total amount (100 wt %) of the monomer component(s). By adjusting the total content thereof to 15 wt % or more, the pressure-sensitive adhesive layer containing the resulting acrylic polymer can have still more excellent pressure-sensitive adhesive property at a low temperature on the order of −30° C., and the pressure-sensitive adhesive force is more easily decreased at a temperatures on the order of −50° C. or less, thereby allowing the removal thereof more easily.
The total content of the polar group-containing monomers and the alicylic monomers means the content of the polar group-containing monomer when only the polar group-containing monomer is included, while it means the total content of the polar group-containing monomer and the alicyclic monomer when both of the polar group-containing monomer and the alicyclic monomer are included.
The content of the polar group-containing monomer in the monomer component(s) is not particularly limited, and the content thereof is, for example, preferably 7 wt % or more (e.g. from 7% to 30 wt %), more preferably from 8% to 25 wt %, still more preferably from 10% to 20 wt %, with respect to the total amount (100 wt %) of the monomer component(s). By adjusting the content to fall within the range of 7% to 30 wt %, still more excellent pressure-sensitive adhesive properties can be achieved in a temperature range of about −30° C. to room temperature. In addition, there may be cases where the pressure-sensitive adhesive layer containing the resulting acrylic polymer can inhibit excessive increase of the pressure-sensitive adhesive force with the lapse of time. It is preferable that the total content of the hydroxyl group-containing monomer and the nitrogen atom-containing monomer in the monomer component(s) falls within the range specified above.
If the tertiary amino group-containing monomer as recited above is included as the polar group-containing monomers, the content thereof is not particularly limited, but is preferably more than 0 wt % and 10 wt % or less, more preferably more than 0 wt % and 5 wt % or less, further preferably more than 0 wt % and 3 wt % or less, with respect to the total amount (100 wt %) of the monomer component(s). By controlling the content to 10 wt % or less, the resulting pressure-sensitive adhesive layer becomes resistant to yellowing.
The proportion of the tertiary amino group-containing monomer to the polar group-containing monomers is not particularly limited, but is preferably more than 0 wt % and 20 wt % or less, more preferably more than 0 wt % and 18 wt % or less, further preferably more than 0 wt % and 16 wt % or less, with respect to the total amount (100 wt %) of the polar group-containing monomers. If the tertiary amino group-containing monomer is included in the polar group-containing monomers, the pressure-sensitive adhesive force with respect to polarizing plates can be increased.
The content of the polar group-containing monomers in the monomer component(s) may also be from 15% to 30 wt % (preferably 20% to 30 wt %) with respect to the total amount (100 wt %) of the monomer component(s). If the content of the polar group-containing monomer is within such a range with respect to the total amount (100 wt %) of the monomer component(s), the resulting pressure-sensitive adhesive sheet may have still more excellent pressure-sensitive adhesive properties in a temperature range of about −30° C. to room temperature and can inhibit the excessive increase of the pressure-sensitive adhesive force with the lapse of time, and hydrophilic properties of the resulting pressure-sensitive adhesive may be enhanced to thereby result in improvement of white-turbidity resistance under humidified conditions and the elastic modulus thereof may be heightened, thereby achieving excellent workability.
If the alicyclic monomers are included in the monomer component(s), the content thereof is not particularly limited, but is preferably more than 0 wt % and 43 wt % or less, more preferably from 5% to 35 wt %, further preferably from 8% to 30 wt %, particularly preferably from 10% to 20 wt %, with respect to the total amount (100 wt %) of the monomer component(s). By controlling the content of the alicyclic monomer to 43 wt % or less, the pressure-sensitive adhesive layer containing the resulting acrylic polymer can have a still more moderate elastic modulus and develop still higher pressure-sensitive adhesive force at an ordinary temperature (about 23° C.).
If the polyfunctional monomer as recited above is included in the monomer component(s), the content thereof is not particularly limited, but is preferably more than 0 wt % and 1 wt % or less, more preferably from 0.001% to 0.1 wt %, further preferably from 0.01% to 0.08 wt %, with respect to the total amount (100 wt %) of the monomer component(s). It is preferable that the content of the polyfunctional monomer is controlled to 1 wt % or less because an excessive increase of a gel fraction of the acrylic polymer produced by polymerizing such monomer components can be inhibited and the step absorbability of the pressure-sensitive adhesive layer containing the acrylic polymer can be easily improved. If a crosslinking agent is used, the polyfunctional monomer may not be used, but if a crosslinking agent is not used, it is preferable to use the polyfunctional monomer in the content range specified above.
Among them, if the content of the polar group-containing monomer in the monomer component(s) is from 15% to 30 wt % (preferably from 20% to 30 wt %) with respect to the total amount (100 wt %) of the monomer component(s) and the content of the alicyclic monomer in the monomer component(s) is more than 0 wt % and 10 wt % or less with respect to the total amount (100 wt %) of the monomer component(s), the hydrophilic properties of the resulting pressure-sensitive adhesive can be enhanced to thereby improve white-turbidity resistance under humidified conditions, and the high elastic modulus thereof can be increased to thereby achieve excellent workability.
In other words, the acrylic polymer produced by polymerizing the monomer component(s) contains at least a structural unit derived from the C10-13 alkyl (meth)acrylate and a structural unit derived from the polar group-containing monomer other than the carboxyl group-containing monomer. The acrylic polymer produced by polymerizing the monomer component(s) may further contain a structural unit derived from the alicyclic monomer, a structural unit derived from the polyfunctional monomer and a structural unit derived from the other monomer. In addition, it is preferred that the acrylic polymer does not substantially contain a structural units derived from the carboxyl group-containing monomer. Each of those structural units may contain one kind of a structural unit, or two or more kinds of structural units.
The content of the structural units derived from the C10-13 alkyl (meth)acrylate in the acrylic polymer produced by polymerizing the monomer component(s) (100 wt %) is preferably 40 wt % or more and less than 80 wt %, more preferably from 45% to 78 wt %, still more preferably from 50% to 76 wt %.
The total content of the structural units derived from the polar group-containing monomers and structural units derived from the alicyclic monomers is preferably 15 wt % or more (e.g. from 15% to 50 wt %), more preferably from 18% to 40 wt %, still more preferably from 20% to 30 wt %.
The content of the structural units derived from the polar group-containing monomers is preferably 7 wt % or more (e.g. from 7% to 30 wt %), more preferably from 8% to 25 wt %, still more preferably from 10% to 20 wt %. The content of structural units derived from the polar group-containing monomers may be in a range of 15% to 30 wt % (further preferably 20% to 30 wt %).
If the structural units derived from the alicyclic monomers are included, the content thereof is not particularly limited, but is preferably more than 0 wt % and 43 wt % or less, more preferably from 5% to 35 wt %, further preferably from 8% to 30 wt %, particularly preferably from 10% to 20 wt %.
If the structural units derived from the polyfunctional monomers are included, the content thereof is not particularly limited, but is preferably more than 0 wt % and 1 wt % or less, more preferably from 0.001% to 0.1 wt %, further preferably from 0.01% to 0.08 wt %.
The content of the structural units derived from the polar group-containing monomers may be from 15% to 30 wt % (preferably from 20% to 30 wt %), and the content of the structural units derived from the alicyclic monomers may be more than 0 wt % and 10 wt % or less. The structural units derived from the alicyclic monomers may not be contained so long as the content of the structural units derived from polar group-containing monomers is from 15% to 30 wt % (further preferably from 20% to 28 wt %).
The C10-13 alkyl (meth)acrylate is supposed to have a crystal-fusion temperature on the order of −60° C. to 20° C., and the side chain thereof has crystallizing properties (side-chain crystallinity) at a temperature on the order of −60° C. to 20° C. As a result, acrylic polymers formed from the C10-13 alkyl (meth)acrylate have the pressure-sensitive adhesive properties at an ordinary temperature, and the elastic modulus thereof become high at temperatures on the order of −30° C., and the pressure-sensitive adhesive force is decreased thereby to occur the separation easily, whereby the acrylic polymers have reworkability.
It is thought that, by including the C10-13 alkyl (meth)acrylate, the polar group-containing monomer with the content falling within the above range, the alicylic monomer with the content such that the total content of the polar group-containing monomer and alicylic monomer falls within the above range, in the monomer component(s) to form the acrylic polymer, the side chain of the C10-13 alkyl (meth)acrylate is hard to be crystallized in a wide range of about −30° C. to ordinary temperatures, thereby the crystal-fusion temperature is shifted to a lower temperature. As a result, the acrylic polymer can have still more excellent pressure-sensitive adhesive properties in a temperature range of about −30° C. to room temperature (23° C.). At a low temperature on the order of −50° C., the side chain of the C10-13 alkyl (meth)acrylate is crystallized, and thus, the acrylic polymer comes to have a high elastic modulus, and the pressure-sensitive adhesive force thereof is decreased thereby to occur the separation easily, and the reworkability is improved.
Thus, the pressure-sensitive adhesive layer formed from the pressure-sensitive adhesive composition containing the acrylic polymer produced by polymerizing the monomer component(s) or a partial polymerization product of the monomer component(s) has excellent pressure-sensitive adhesive properties in a temperature range of about −30° C. to an ordinary temperature, and the pressure-sensitive adhesive force thereof is easily decreased thereby to occur the separation easily at a low temperature on the order of −50° C., and thus, the excellent reworkability at a low temperature on the order of −50° C. is achieved.
Although the use of monomer component(s) including C10-13 alkyl (meth)acrylate as the essential component is mentioned in the foregoing embodiments, the scope of the present invention should not be construed as being limited to these embodiments. For example, there are cases where effects similar to the above effects can be also achieved by appropriately using the C1-9 alkyl (meth)acrylate and the C14-24 alkyl (meth)acrylate in combination, instead of using the C10-13 alkyl (meth)acrylate. Examples of the C1-9 alkyl (meth)acrylate and the C14-24 alkyl (meth)acrylate include those recited hereinbefore.
The acrylic polymer produced by polymerizing the monomer component(s) can be prepared by polymerizing, e.g., the monomer component as mentioned above or a partial polymerization product of the monomer component(s) (e.g. a mixture of the monomer component(s) with a partial polymerization product of the monomer component(s)) in accordance with conventional polymerization methods. Examples of a method for polymerizing the monomer component(s) include a solution polymerization method, an emulsion polymerization method, a bulk polymerization method, and polymerization methods by an active energy-ray irradiation (e.g. a thermal polymerization method and an active energy-ray polymerization method). Of these methods, a solution polymerization method and an active energy-ray polymerization method are preferable in terms of transparency, water resistance, costs and so on. Although the monomer component(s) and the partial polymerization product of the monomer component(s) are not particularly limited, it is preferred that the polymerization be performed so as to avoid contact with oxygen (e.g. in an atmosphere of nitrogen).
As the active energy-ray irradiated in the active energy-ray polymerization (photopolymerization), examples thereof include an alpha ray, a beta ray, a gamma ray, a neutron ray, an ionizing radiation such as an electron ray, and UV, and UV is preferable. An irradiation energy, an irradiation time and an irradiation method of the active energy-ray are not particularly limited so long as the monomer component(s) may be reacted by activating a photopolymerization initiator.
In the solution polymerization, various kinds of general solvents can be used. Examples of such a solvent include organic solvents such as: esters such as ethyl acetate and n-butyl acetate; aromatic hydrocarbons such as toluene and benzene; aliphatic hydrocarbons such as n-hexane and n-heptane; alicyclic hydrocarbons such as cyclohexane and methylcyclohexane; and ketones such as methylethylketone and methylisobutylketone. The solvents may be used either alone or in combination of two or more thereof
When the monomer component(s) is polymerized, a polymerization initiator such as a photopolymerization initiator (photoinitiator) or a thermal polymerization initiator may be used depending on the kind of polymerization reaction. The polymerization initiator may be used alone or in combination of two or more thereof
The photopolymerization initiator is not particularly limited, and examples thereof include a benzoin ether photopolymerization initiator, an acetophenon photopolymerization initiator, an α-ketol photopolymerization initiator, an aromatic sulfonyl chloride photopolymerization initiator, a photoactive oxime photopolymerization initiator, a benzoin photopolymerization initiator, a benzyl photopolymerization initiator, a benzophenon photopolymerization initiator, a ketal photopolymerization initiator and a thioxantone photopolymerization initiator. The content of the photopolymerization initiator used is not particularly limited, but is preferably 0.01 to 1 parts by weight, and more preferably 0.05 to 0.5 parts by weight with respect to the total amount (100 parts by weight) of the monomer component(s).
As the benzoin ether photopolymerization initiator, examples thereof include benzoin methyl ether, benzoin ethyl ether, benzoin propyl ether, benzoin isopropyl ether, benzoin isobutyl ether, and 2,2-dimethoxy-1,2-diphenylethane-1-on. As the acetophenon photopolymerization initiator, examples thereof include 2,2-diethoxyacetophenon, 2,2-dimethoxy-2-phenylacetophenon, 1-hydroxycyclohexylphenylketone (α-hydroxycyclohexyl phenyl ketone), 4-phenoxydichloroacetophenon and 4-(t-butyl)dichloroacetophenon. As the α-ketol photopolymerization initiator, examples thereof include 2-methyl-2-hydroxypropiophenon and 1-[4-(2-hydroxyethyl)phenyl]-2-methylpropane-1-on. As the aromatic sulfonyl chloride photopolymerization initiator, examples thereof include 2-naphthalenesulfonyl chloride. As the photoactive oxime photopolymerization initiator, examples thereof include 1-phenyl-1,1-propanedion-2-(o-ethoxycarbonyl)-oxime. As the benzoine photopolymerization initiator, examples thereof include benzoin. As the benzyl photopolymerization initiator, examples thereof include benzyl. As the benzophenon photopolymerization initiator, examples thereof include benzophenon, benzoylbenzoate, 3,3′-dimethyl-4-methoxybenzophenon and polyvinylbenzophenon. As the ketal photopolymerization initiator, examples thereof include benzyl dimethyl ketal. As the thioxantone photopolymerization initiator, examples thereof include thioxantone, 2-chlorothioxantone, 2-methylthioxantone, 2,4-dimethylthioxantone, isopropylthioxantone, 2,4-diisopropylthioxantone and dodecylthioxantone.
As the thermal polymerization initiator, examples thereof include an azo-based polymerization initiator, a peroxide-based polymerization initiator (for example, dibenzoyl peroxide and tert-butyl permaleate) and a redox-based polymerization initiator. Among the initiators, the azo-based polymerization initiator disclosed in JP-A-2002-69411 is preferable. As the azo-based polymerization initiator, examples thereof include 2,2′-azobisisobutyronitrile, 2,2′-azobis-2-methylbutyronitrile, dimethyl 2,2′-azobis(2-methylpropionate) and 4,4′-azobis-4-cyanovaleric acid. The content of the thermal polymerization initiator used is not particularly limited, and is preferably 0.05 to 0.5 parts by weight, and more preferably 0.1 to 0.3 parts by weight with regard to the total amount (100 parts by weight) of the monomer component(s).
The acrylic polymer is not particularly limited, and for example, is used as an essential component in the pressure-sensitive adhesive composition.
The partial polymerization product is a partial polymerization product constituted of (formed from) the monomer component(s). The partial polymerization product can be made into an acrylic polymer in accordance with the polymerization method as mentioned above (e.g. active energy-ray polymerization method).
The degree of polymerization of the monomer component(s) in the partial polymerization product is not particularly limited, but is preferably from 5% to 20 wt %, more preferably from 5% to 15 wt %, in terms of the viscosity suitable for handling and coating of the pressure-sensitive adhesive composition.
The degree of polymerization can be determined as follows.
A portion of the partial polymerization product is taken out as a sample. The weight of the sample is determined by precise weighing and referred to as “weight of partial polymerization product before being dried”. And then the sample is dried at 130° C. for 6 hours, and the weight of the thus dried sample is determined by precise weighing and referred to as “weight of the partial polymerization product after being dried”. Then, the weight of the sample reduced in weight by drying at 130° C. for 2 hours is determined from “weight of the partial polymerization product before being dried” and “weight of the partial polymerization product after being dried”, and referred to as “weight decrement” (the total weight of volatile ingredients and unreacted monomers). The degree of polymerization (wt %) of the partial polymerization product of the monomer component(s) is determined from the thus obtained “weight of the partial polymerization product before being dried” and “weight decrement” according to the following expression.
Degree of polymerization (wt %) of the partial polymerization product of the monomer component(s)=[1−(weight decrement)/(weight of the partial polymerization product before being dried)]×100
The partial polymerization product is not particularly limited, and for example, is used as an essential component in the pressure-sensitive adhesive composition.
The pressure-sensitive adhesive composition may include a crosslinking agent. The crosslinking agent is not particularly limited, and examples thereof include isocyanate-based crosslinking agents, epoxy-based crosslinking agents, melamine-based crosslinking agents, peroxide-based crosslinking agents, urea-based crosslinking agents, metal alkoxide-based crosslinking agents, metal chelate-based crosslinking agents, metal salt-based crosslinking agents, carbodiimide-based crosslinking agents, oxazoline-based crosslinking agents, aziridine-based crosslinking agents and amine-based crosslinking agents. Of these crosslinking agents, isocyanate-based crosslinking agents and epoxy-based crosslinking agents are preferred. Such crosslinking agents may be used alone, or in combination of two or more thereof.
As the isocyanate-based crosslinking agent (polyfunctional isocyanate compound), examples thereof include lower aliphatic polyisocyanates such as 1,2-ethylene diisocyanate, 1,4-butylenediisocyanate and 1,6-hexamethylene diisocyanate; alicyclic polyisocyanates such as cyclopentylene diisocyanate, cyclohexylene diisocyanate, isophorone diisocyanate, hydrogenated tolylene diisocyanate and hydrogenated xylene diisocyanate; and aromatic polyisocyanates such as 2,4-tolylene diisocyanate, 2,6-tolylene diisocyanate, 4,4′-diphenylmethane diisocyanate and xylylene diisocyanate. In addition thereto, a trimethylolpropane/tolylene diisocyanate adduct (manufactured by Nippon Polyurethane Industry Co., Ltd., trade name “CORONATE L” or the like), and a trimethylolpropane/hexamethylene diisocyanate adduct (manufactured by Nippon Polyurethane Industry Co., Ltd., trade name “CORONATE HL” or the like) may also be used.
As the epoxy-based crosslinking agent (polyfunctional epoxy compound), examples thereof include N,N,N′,N′-tetraglycidyl-m-xylenediamine, diglycidyl aniline, 1,3-bis(N,N-diglycidylaminomethyl)cyclohexane, 1,6-hexanediol diglycidyl ether, neopentyl glycol diglycidyl ether, ethylene glycol diglycidyl ether, propylene glycol diglycidyl ether, polyethylene glycol diglycidyl ether, polypropylene glycol diglycidyl ether, sorbitol polyglycidyl ether, glycerol polyglycidyl ether, pentaerythritol polyglycidyl ether, polyglycerol polyglycidyl ether, sorbitan polyglycidyl ether, trimethylolpropane polyglycidyl ether, adipic acid diglycidyl ester, o-phthalic diglycidyl ester, triglycidyl-tris(2-hydroxyethyl)isocyanurate, resorcin diglycidyl ether, bisphenol-S-diglycidyl ether and an epoxy-based resin having two or more epoxy groups in the molecule. As commercially available products thereof, trade name “TETRAD C” manufactured by Mitsubishi Gas Chemical Company, Inc. may be used.
The content of the crosslinking agent is not particular limited, and is preferably from 0.001 to 10 parts by weight, preferably from 0.01 to 3 parts by weight, with respect to the total amount (100 parts by weight) of the monomer component(s), from the viewpoint of adjusting the gel fraction of the pressure-sensitive adhesive layer of the present invention to a range within a favorable range.
The pressure-sensitive adhesive composition may include a silane coupling agent from the viewpoint of further improving the pressure-sensitive adhesive properties under the humidified environment at temperatures ranging from about −30° C. to room temperature. The silane coupling agent is not particularly limited, and examples thereof include silane coupling agents with functional groups (such as a vinyl group, an epoxy group, an amino group, a mercapto group, an acryloxy group, a methacryloxy group, an isocyanato group, a styryl group and a polysulfide group). Of these, the silane coupling agents with epoxy groups (epoxy group-containing silane coupling agents) are preferred from the viewpoint of improving the pressure-sensitive adhesive properties particularly with respect to a glass adherend. More specifically, examples thereof include vinyl group-containing silane coupling agents, such as vinyltrimethoxysilane; epoxy group-containing silane coupling agents, such as γ-glycidoxypropyltrimethoxysilane and γ-glycidoxypropyltriethoxysilane; amino group-containing silane coupling agents, such as γ-aminopropyltrimethoxysilane and N-β(aminoethyl) γ-aminopropyltrimethoxysilane; mercapto group-containing silane coupling agents, such as γ-mercaptopropylmethyldimethoxysilane; acryloxy group-containing silane coupling agents, such as γ-acryloxypropyltrimethoxysilane; methacryloxy group-containiing silane coupling agents, such as γ-methacryloxypropyltriethoxysilane; isocyanato group-containing silane coupling agents, such as 3-isocyanatopropyltriethoxysilane; styryl group-containing silane coupling agents, such as p-styryltrimethoxysilane; and polysulfide group-containing silane coupling agents, such as bis(triethoxysilylpropyl)tetrasulfide. These silane coupling agents may be used alone, or in combination of two or more thereof.
The content of the silane coupling agent is not particularly limited, but is preferably from 0.01 to 2 parts by weight, more preferably from 0.03 to 1 parts by weight, with respect to the total amount (100 parts by weight) of the monomer component(s).
The pressure-sensitive adhesive composition of the present invention may include an oligomer from the viewpoint of improving the pressure-sensitive adhesive properties at room temperature. The oligomer is an oligomer (polymer) different from the above-described acrylic polymer and partial polymerization products of the monomer component(s). The word “different” used above means that the oligomer does not completely same as the acrylic polymer and the partial polymerization products in terms of constituent monomers and their contents.
The oligomer is not particularly limited, and is preferably an oligomer containing, as essential monomer components, (meth)acrylic acid ester having a ring structure in its molecule (which is referred to as “ring-containing (meth)acrylic acid ester” in some cases) and alkyl (meth)acrylate containing a straight- or branched-chain alkyl group.
The ring-containing (meth)acrylic acid ester is not particularly limited, and examples thereof include cycloalkyl (meth)acrylate, such as cyclopentyl (meth)acrylate, cyclohexyl (meth)acrylate, cycloheptyl (meth)acrylate and cyclooctyl (meth)acrylate; (meth)acrylic acid ester having a bicyclic aliphatic hydrocarbon ring, such as isobornyl (meth)acrylate; (meth)acrylic acid ester having tri- or multi-cyclic aliphatic hydrocarbon ring, such as dicyclopentanyl (meth)acrylate, dicyclopentanyloxyethyl (meth)acrylate, tricyclopentanyl (meth)acrylate, 1-adamantyl (meth)acrylate, 2-methyl-2-adamantyl (meth)acrylate and 2-ethyl-2-adamantyl (meth)acrylate; and (meth)acrylic acid ester having an aromatic ring, such as aryl (meth)acrylate such as phenyl (meth)acrylate, aryloxyalkyl (meth)acrylate such as phenoxyethyl (meth)acrylate, and arylalkyl (meth)acrylate such as benzyl (meth)acrylate. Among them, (meth)acrylic acid ester having a tri- or multi-cyclic aliphatic hydrocarbon ring (particularly, tri- or multi-crosslinking hydrocarbon ring) is preferable from the viewpoint of making it hard to cause inhibition of polymerization, and dicyclopentanyl methacrylic acid (DCPMA) is more preferred. The ring-containing (meth) acrylic acid ester may be used either alone, or in combination of two or more thereof.
The content of the ring-containing (meth)acrylic acid ester is not particularly limited, but is preferably e.g. from 10% to 90 wt %, more preferably from 20% to 80 wt %, further preferably from 35% to 80 wt %, with respect to the total amount (100 wt %) of monomer component(s) to form the oligomer.
The alkyl (meth)acrylate containing a straight- or branched-chain alkyl group in the oligomer is not particularly limited, and examples thereof include alkyl (meth)acrylates having an alkyl group (straight- or branched-chain alkyl group) having 1 to 20 carbon atoms, such as methyl (meth)acrylate, ethyl (meth)acrylate, propyl (meth)acrylate, isopropyl (meth)acrylate, butyl (meth)acrylate, isobutyl (meth)acrylate, s-butyl (meth)acrylate, t-butyl (meth)acrylate, pentyl (meth)acrylate, isopentyl (meth)acrylate, hexyl (meth)acrylate, heptyl (meth)acrylate, octyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, isooctyl (meth)acrylate, nonyl (meth)acrylate, isononyl (meth)acrylate, decyl (meth)acrylate, isodecyl (meth)acrylate, undecyl (meth)acrylate, dodecyl (meth)acrylate, tridecyl (meth)acrylate, tetradecyl (meth)acrylate, pentadecyl (meth)acrylate, hexadecyl (meth)acrylate, heptadecyl (meth)acrylate, octadecyl (meth)acrylate, nonadecyl (meth)acrylate and eicosyl (meth)acrylate. Of these, methyl methacrylate (MMA) is preferred. The alkyl (meth)acrylate containing a straight- or branched-chain alkyl group may be used alone, or in combination of two or more thereof.
The content of the alkyl (meth)acrylate containing a straight- or branched-chain alkyl group in the oligomer is not particularly limited, but is preferably from 10% to 90 wt %, more preferably from 20% to 80 wt %, further preferably from 20% to 60 wt %, with respect to the total amount (100 wt %) of monomer component(s) to form the oligomer, from the viewpoint of allowing the pressure-sensitive adhesive layer to have a moderate elastic modulus.
The monomer component(s) to form the oiligomer is not particularly limited, and examples thereof may further include alkoxyalkyl (meth)acrylate, a carboxyl group-containing monomer, an amido group-containing monomer, an amino group-containing monomer, a cyano group-containing monomer, a sulfonic group-containing monomer, a phosphoric group-containing monomer, an isocyanato group-containing monomer, an imide group-containing monomer and the like.
The oligomer can be formed by polymerizing such monomer component(s) to form the oligomer in accordance with a conventional polymerization method. Examples of the polymerization method for obtaining the oligomer include a solution polymerization method, an emulsion polymerization, a bulk polymerization method and polymerization methods by an active energy-ray irradiation (e.g. an active energy-ray polymerization method).
On the occasion of polymerization for forming the oligomer, various kinds of general solvents can be used. Examples thereof include organic solvents, such as esters such as ethyl acetate and n-butyl acetate, aromatic hydrocarbons such as toluene and benzene, aliphatic hydrocarbons such as n-hexane and n-heptane, alicyclic hydrocarbons such as cyclohexane and methylcyclohexane, and ketones such as methyl ethyl ketone and methyl isobutyl ketone. These solvents may be used alone, or in combination of two or more thereof
Further, on the occasion of polymerization for forming the oligomer, a conventional polymerization initiator may be used. Examples of the polymerization initiator include: azo-based initiators such as 2,2′-azobisisobutyronitrile (AIBN), 2,2′-azobis-2-methylbutyronitrile (AMBN), dimethyl 2,2′-azobis(2-methylpropionate), 4,4′-azobis-4-cyanovalerianic acid, 2,2′-azobis(4-methoxy-2,4-dimethylvaleronitrile), 2,2′-azobis(2,4-dimethylvaleronitrile), 1,1′-azobis(cyclohexane-1-carbonitrile) and 2,2′-azobis(2,4,4-trimethylpentane); and peroxide-based initiators, such as benzoyl peroxide, t-butyl hydroperoxide, di-t-butyl peroxide, t-butyl peroxybenzoate, dicumyl peroxide, 1,1-bis(t-butylperoxy)-3,3,5-trimethylcyclohexane and 1,1-bis(t-butylperoxy)cyclododecane. In the case of the solution polymerization, an oil-soluble polymerization initiator is preferably used. Those polymerization initiators may be used alone, or in combination of two or more thereof. The used amount of the polymerization initiator is not particularly limited as long as the used amount falls within a usual range. For instance, the used amount is chosen appropriately from the range of 0.1 to 15 parts by weight with respect to the total amount (100 parts by weight) of monomer component(s) forming the oligomer.
On the occasion of polymerization for forming the oligomer, a chain transfer agent can be used for the purpose of controlling its molecular weight. As the chain transfer agent, examples thereof include 2-mercaptoethanol, α-thioglycerol, 2,3-dimercapto-1-propanol, octyl mercaptan, t-nonyl mercaptan, dodecyl mercaptan (lauryl mercaptan), t-dodecyl mercaptan, glycidyl mercaptan, thioglycolic acid, methyl thioglycolate, ethyl thioglycolate, propyl thioglycolate, butyl thioglycolate, t-butyl thioglycolate, 2-ethylhexyl thioglycolate, octyl thioglycolate, isooctyl thioglycolate, decyl thioglycolate, dodecyl thioglycolate, thioglycolic acid ester of ethylene glycol, thioglycolic acid ester of neopentyl glycol, thioglycolic acid ester of pentaerythritol, and α-methylstyrene dimer. Among them, thioglycolic acid and α-thioglycerol are preferred. Those chain transfer agents may be used alone, or in combination of two or more thereof.
The content (used amount) of the chain transfer agent is not particularly limited, but is preferably from 0.1 to 20 parts by weight, more preferably from 0.2 to 15 parts by weight, further preferably from 0.3 to 10 parts by weight, with respect to the total amount (100 parts by weight) of monomer component(s) to form the oligomer, from the viewpoint of controlling the molecular weight of the oligomer to an appropriate range.
The weight-average molecular weight (Mw) of the oligomer is preferably from 1,000 to 30,000, more preferably from 1,000 to 20,000, further preferably from 1,500 to 10,000, still further preferably from 2,000 to 4,000. By controlling the weight-average molecular weight of the oligomer to 1,000 or more, the pressure-sensitive adhesive force and retention properties are enhanced. By controlling the weight-average molecular weight of the oligomer to 30,000 or less, the pressure-sensitive adhesive force at room temperature is enhanced.
The weight-average molecular weight of the oligomer can be measured by gel permeation chromatography (GPC). More specifically, a measurement is performed by using e.g. a GPC measurement device, HLC-8120GPC (trade name, a product of Tosoh Corporation), under the following conditions, and then, the weight-average molecular weight of the oligomer can be calculated by standard polystyrene conversion value.
Sample concentration: About 2.0 g/L (tetrahydrofuran solution)
Amount of sample injected: 20 μL
Column: TSK GEL, SUPER AWM-H+SUPER AW4000+SUPER AW2500, trade names, products of Tosoh Corporation
Column size: Each 6.0 mm I.D.×150 mm
Eluent: Tetrahydrofuran (THF)
Flow rate: 0.4 mL/min
Detector: Refractive index (RI) detector
Column temperature (measurement temperature): 40° C.
The glass transition temperature (Tg) of the oligomer is not particularly limited, but is preferably from 20° C. to 300° C., more preferably from 30° C. to 300° C., further preferably from 40° C. to 300° C. By adjusting the glass transition temperature of the oligomer to 20° C. or more, there is a tendency that the pressure-sensitive adhesive force at room temperature is improved. By controlling the glass transition temperature of the oligomer to 300° C. or less, there is a tendency that the pressure-sensitive adhesive layer can have moderate flexibility and the pressure-sensitive adhesive force and step absorbability thereof are improved.
The glass transition temperature (Tg) of the oligomer is a glass transition temperature (theoretical value) represented by the following equation.
1/Tg=W1/Tg1+W2/Tg2+ . . . +Wn/Tgn
In the equation, Tg stands for the glass transition temperature (unit: K) of the oligomer, Tgi stands for the glass transition temperature (unit: K) of a homopolymer formed from a monomer i, and Wi stands for the weight fraction of the monomer i with respect to the total weight of the monomer component(s) (i=1, 2, . . . , n). The foregoing is an expression for calculation in the case of the oligomer formed from n kinds of monomer components, namely a monomer 1, a monomer 2, . . . , and a monomer n.
The content of the oligomer in the pressure-sensitive adhesive composition is not particularly limited, but is preferably from 1 to 10 parts by weight, more preferably from 1.5 to 8 parts by weight, further preferably from 2 to 5 parts by weight, with respect to the total amount (100 parts by weight) of the monomer component(s) to form the acrylic polymer, from the viewpoint of enhancing the compatibility with the acrylic polymer and enhancing the pressure-sensitive adhesive force at room temperature. The amount of the acrylic polymer in the pressure-sensitive adhesive composition is equal to the total of monomer component(s) to form the acrylic polymer.
The pressure-sensitive adhesive composition may include a solvent. The solvent is not particularly limited, and examples thereof include organic solvents, such as esters such as ethyl acetate and n-butyl acetate, aromatic hydrocarbons such as toluene and benzene, aliphatic hydrocarbons such as n-hexane and n-heptane, alicyclic hydrocarbons such as cyclohexane and methylcyclohexane, ketones such as methyl ethyl ketone and methyl isobutyl ketone, and alcohols such as methanol and butanol. These solvents may be used alone, or in combination of two or more thereof.
The pressure-sensitive adhesive composition may include well-known additives (other additives) so long as the inclusion thereof does not impair the effects of the present invention, and examples thereof include a crosslinking accelerator, a tackifying resin (e.g. a rosin derivative, a polyterpene resin, a petroleum resin, oil-soluble phenol), an anti-aging agent, a filler, a coloring agent (such as pigments and dyes), a UV absorbent, an oxidation inhibitor, a chain transfer agent, a plasticizer, a softening agent, a surfactant and an antistatic agent.
The preparation method of the pressure-sensitive adhesive composition is not particularly limited, and examples thereof include a method by mixing: the acrylic polymer produced by polymerizing the monomer component(s) or the partial polymerization product of the monomer component(s) which is an essential component; and the monomer component(s), the polymerization initiator, the silane coupling agent, the oligomer, the solvent, the crosslinking agent, the additives and the like which may be added if needed. The preparation method of the pressure-sensitive adhesive composition containing, as the essential component, the acrylic polymer obtained by polymerizing the monomer component(s) is not particularly limited, and examples thereof include a method by solving, in a solvent: the acrylic polymer produced by polymerizing the monomer component(s); and the monomer component, the crosslinking agent, the silane coupling agent, the oligomer, the additive and the like which may be added if needed. The preparation method of the pressure-sensitive adhesive composition containing, as the essential component, the partial polymerization product of the monomer component(s) is not particularly limited, and examples thereof include a method by mixing: the partial polymerization product of the monomer component(s); and the monomer components, the polymerization initiator, the silane coupling agent, the oligomer, the solvent, the crosslinking agent, the additives and the like which may be added if needed.
The content of the acrylic polymer in the pressure-sensitive adhesive layer of the present invention is not particularly limited, but is preferably, e.g. 50 wt % or more, more preferably 60 wt % or more, further preferably 80 wt % or more, with respect to the total weight (100 wt %) of the pressure-sensitive adhesive layer, from the viewpoint of allowing formation of a pressure-sensitive adhesive layer still more excellent in the pressure-sensitive adhesive properties at temperatures ranging from about −30° C. to room temperature)(23° as well as reworkability at temperatures on the order of −50° C. or less, and moreover excellent in step absorbability.
The pressure-sensitive adhesive layer of the present invention is formed by subjecting the pressure-sensitive adhesive composition containing the acrylic polymer to drying, curing and so on. Alternatively, the pressure-sensitive adhesive layer of the present invention is formed via the production of acrylic polymer by subjecting the pressure-sensitive adhesive composition containing a partial polymerization product of the monomer component(s) to curing (e.g. thermosetting or curing by irradiation with active energy rays such as UV rays).
The melting point of the pressure-sensitive adhesive layer of the present invention is from −60° C. to 0° C., preferably from −50° C. to −10° C., more preferably from −40° C. to −15° C. or from −30° C. to −10° C. If the melting point thereof is more than 0° C., the pressure-sensitive adhesive force cannot be developed in a temperature range of −30° C. to room temperature. The measurement of the melting point is not particularly limited, and the melting point can be measured by using the pressure-sensitive adhesive layer as a measurement sample according to differential scanning calorimetry (DSC) in conformity with JIS K 7121. Specifically, the measurement can be carried out e.g. by using a measurement device, Q-2000 (trade name, a product of TA Instruments, Inc.) under the condition of rate of temperature rise of 10° C./min from −80° C. to 80° C. More specifically, the melting point can be measured by the method described later in the section “Evaluations” under “(5) Melting point”.
The thickness of the pressure-sensitive adhesive layer of the present invention is not particularly limited, but is preferably from 10 μm to 1 mm, more preferably from 100 μm to 500 μm, further preferably from 150 μm to 350 μm. By adjusting the thickness to 10 μm or more, the pressure-sensitive adhesive layer can have excellent step absorbability. By controlling the thickness to 1 mm or less, the pressure-sensitive adhesive layer resists deformation, and workability thereof can be enhanced.
The gel fraction of the pressure-sensitive adhesive layer of the present invention is not particularly limited, but is preferably from 20% to 90 wt %, more preferably from 30% to 85 wt %, further preferably from 40% to 80 wt %. By controlling the gel fraction to 90 wt % or less, the cohesive force of the pressure-sensitive adhesive layer is reduced to some extent, and the pressure-sensitive adhesive layer becomes soft and tends to follow step-difference portions, thereby improving the step absorbability. On the other hand, if the gel fraction thereof is less than 20 wt %, the pressure-sensitive adhesive layer is too soft and workability of the pressure-sensitive adhesive sheet is lowered. In addition, under high-temperature environments or high-temperature high-humidity environments, air bubbles or lift-off tend to be easily occurred, and thus, anti-foaming release property is decreased. The gel fraction can be controlled by, e.g. kinds and contents (usage) of a polyfunctional monomer and/or a crosslinking agent.
The gel fraction (proportion of solvent-insoluble matter) can be determined as a matter insoluble in ethyl acetate. Specifically, the gel fraction is determined as the proportion (unit: wt %) of the weight of insoluble matter after immersion of a sample of the pressure-sensitive adhesive layer in ethyl acetate at room temperature (23° C.) for 7 days to the weight of the sample before the immersion. More specifically, the gel fraction is a value calculated according to the following “Method of measuring gel fraction”.
About 1 g of a portion of the pressure-sensitive adhesive layer is sampled, and the weight thereof is measured and referred to as “weight of pressure-sensitive adhesive layer before immersion”. Next, the sampled pressure-sensitive adhesive layer is immersed in 40 g of ethyl acetate for 7 days, and then, all the matter insoluble in the ethyl acetate (insoluble residues) is collected and all of the collected insoluble residues are dried at 130° C. for 2 hours to thereby remove the ethyl acetate. Thereafter, the weight thereof is measured, and referred to as “dry weight of insoluble residues” (weight of pressure-sensitive adhesive layer after immersion). Then, the gel fraction is calculated according to the following expression.
Gel fraction (wt %)=[(dry weight of insoluble residues)/(weight of pressure-sensitive adhesive layer before immersion)]×100
The weight-average molecular weight of soluble matter (sol matter) in the pressure-sensitive adhesive layer of the present invention is not particularly limited, but is preferably from 1.0×105 to 5.0×106, more preferably from 2.0×105 to 2.0×106, further preferably from 3.0×105 to 1.0×106. If the weight-average molecular weight of the sol matter is less than 1.0×105, there may be cases where the pressure-sensitive adhesive force is reduced. If the weight-average molecular weight of the sol matter is more than 5.0×106, there may be cases where the elastic modulus thereof is increased and the pressure-sensitive adhesive force is decreased.
The “weight average molecular weight of soluble matter (sol matter)” is calculated according to the following measurement method.
About 1 g of a portion of the pressure-sensitive adhesive layer is sampled, wrapped with a porous tetrafluoroethylene sheet having an average pore size of 0.2 NTF1122 (trade name, a product of NITTO DENKO CORPORATION), and then tied with kite string (here, the pressure-sensitive adhesive layer in this state is referred to as “a sample”). Next, the sample is put in a 50-ml container filled with ethyl acetate and left standing for one week (7 days) at 23° C. Thereafter, the ethyl acetate solution (containing the thus extracted sol matter) in the container is taken out and the solvent (ethyl acetate) is volatilized by drying under a reduced pressure, thereby obtaining a sol matter.
The sol matter is dissolved in tetrahydrofuran (THF), and the weight-average molecular weight (Mw) thereof is determined from measurement using a GPC measurement device, HLC-8120GPC (trade name, a product of Tosoh Corporation), under the following conditions with polystyrene conversion value. (GPC measurement conditions)
Sample concentration: 0.2 wt % (tetrahydrofuran solution)
Amount of sample injected: 10 μL
Eluent: Tetrahydrofuran (THF)
Flow rate (flow velocity): 0.6 mL/min
Column temperature (measurement temperature): 40° C.
Column: TSK GEL SUPER HM-H/H4000/H3000/H200, trade names, products of Tosoh Corporation
Detector: Refractive index (RI) detector
The substrate is not particularly limited, and examples thereof include plastic films and various kinds of optical films, such as an antireflection (AR) film, a polarizing plate and a retardation plate. As materials for the plastic films or the like, examples thereof include plastic materials, such as polyester resins such as polyethylene terephthalate (PET), acrylic resins such as polymethyl methacrylate, polycarbonate, triacetyl cellulose, polysulfone, polyarylate, polyimide, polyvinyl chloride, polyvinyl acetate, polyethylene, polypropylene, an ethylene-propylene copolymer, and cyclic olefin polymers such as “ARTON” (trade name, manufactured by JSR Corporation) and “ZEONOR” (trade name, manufactured by ZEON CORPORATION). These plastic materials may be used alone, or in combination of two or more thereof.
The substrate is not particularly limited, but is preferably e.g. a transparent substrate. The “transparent substrate” used herein refers to the substrate having, e.g. a total light transmittance in the visible light wavelength region of preferably 85% or more, more preferably 88% or more, as measured in accordance with JIS K 7361-1. In addition, a haze of the transparent substrate (as measured in accordance with JIS K 7136) is preferably, e.g. 1.5% or less, more preferably 1.0% or less. Examples of the transparent substrate include PET film and non-oriented films such as “ARTON” (trade name, a product of JSR Corporation) and “ZEONOR” (trade name, a product of ZEON CORPORATION).
The thickness of the substrate is not particularly limited, but is preferably from 12 to 75 μm. The substrate may have either a single-layer form or a multiple-layer form. Further, the substrate surface may be appropriately subjected to conventional surface treatment, such as physical treatment such as corona discharge treatment or plasma treatment, or chemical treatment such as undercoating treatment.
The other pressure-sensitive adhesive layers (pressure-sensitive adhesive layers other than the pressure-sensitive adhesive layer of the present invention) is not particularly limited, and examples thereof include conventional pressure-sensitive adhesive layers formed from conventional pressure-sensitive adhesives, such as urethane-based pressure-sensitive adhesives, acrylic pressure-sensitive adhesives, rubber-based pressure-sensitive adhesives, silicone-based pressure-sensitive adhesives, polyester-based pressure-sensitive adhesives, polyamide-based pressure-sensitive adhesives, epoxy-based pressure-sensitive adhesives, vinyl alkyl ether-based pressure-sensitive adhesives and fluorine-based pressure-sensitive adhesives. These other pressure-sensitive adhesives may be used alone, or in combination of two or more thereof
The pressure-sensitive adhesive layer surface (pressure-sensitive adhesive surface) of the pressure-sensitive adhesive sheet of the present invention may be protected with a separator (release liner) until it is used. In the double-sided pressure-sensitive adhesive sheet of the present invention, each pressure-sensitive adhesive surface may be protected by two separators, respectively, or protected in such a way that the surface is wound in a roll form by using one separator of which both sides are release surfaces. The separator is used as a protective material of the pressure-sensitive adhesive layer, and peeled away when the pressure-sensitive adhesive sheet of the present invention is laminated to an adherend. In addition, the separator also plays a role as the substrate of the pressure-sensitive adhesive layer. The separator may not be provided.
Any known release paper may be used as the separator. The separator is not particularly limited, and examples thereof include a substrate having a release treated layer, a low adhesive substrate composed of a fluorine polymer, or a low adhesive substrate composed of a non-polar polymer. As the substrate having the release treated layer, examples thereof include a plastic film or paper whose surface is treated with a release agent such as silicon-based release agent, long-chain alkyl-based release agent, fluorine-based release agent, and molybdenum sulfide-based release agent. As the fluorine-based polymer, examples thereof include polytetrafluoroethylene, polychlorotrifluoroethylene, polyvinyl fluoride, polyvinylidene fluoride, a tetrafluoroethylene-hexafluoropropylene copolymer and a chlorofluoroethylene-vinylidene fluoride copolymer. As the non-polar polymer, examples thereof include an olefin-based resin (for example, polyethylene, polypropylene and the like). The separator can be formed by using a known/general method. The thickness of the separator is not particularly limited.
As a method for manufacturing the pressure-sensitive adhesive sheet of the present invention, a conventional manufacturing method can be applied. The method for manufacturing the pressure-sensitive adhesive sheet of the present invention varies depending on the composition of the pressure-sensitive adhesive, and no particular limitation is imposed thereon. Examples thereof include the following methods (1) to (3). If the pressure-sensitive adhesive sheet of the present invention is a double-sided pressure-sensitive adhesive sheet, the methods for forming each surface of the pressure-sensitive adhesive layers may be the same or different from each other.
(1) A method of forming a pressure-sensitive adhesive composition layer by coating a substrate or a separator with the pressure-sensitive adhesive composition containing a partial polymerization product of monomer component(s) and, as required, monomer components, a polymerization initiator, a solvent, a crosslinking agent, a silane coupling agent, an oligomer, additives and the like, followed by curing (e.g. thermal curing or curing by the irradiation of active energy rays such as ultraviolet rays) the pressure-sensitive adhesive composition layer, thereby forming the pressure-sensitive adhesive layer.
(2) A method of forming a pressure-sensitive adhesive layer by coating a substrate or a separator with a pressure-sensitive adhesive composition (solution) prepared by solving, in a solvent, an acrylic polymer and, as required, monomer component(s), a crosslinking agent, additives, a silane coupling agent and an oligomer, followed by drying and/or curing the pressure-sensitive adhesive composition.
(3) A method of further drying the pressure-sensitive adhesive sheet manufactured by the method (1).
As the curing method adopted in the foregoing (1) to (3), preferable examples thereof include methods of curing with active energy rays (particularly, curing with UV rays), from the viewpoint of allowing attainment of excellent productivity and formation of a thick pressure-sensitive adhesive layer. Since curing by the active energy ray may be inhibited by oxygen in air, it is appropriate that oxygen be shut off e.g. by laminating a separator on the pressure-sensitive adhesive layer or being cured in an atmosphere of nitrogen.
The method of manufacturing the pressure-sensitive adhesive sheet of the present invention by using the pressure-sensitive adhesive composition containing the acrylic polymer is not particularly limited, and is preferably e.g. the foregoing method (2). The method of manufacturing the pressure-sensitive adhesive sheet of the present invention by using the pressure-sensitive adhesive composition containing the partial polymerization product is not particularly limited, and is preferably e.g. the foregoing method (1) or (3), more preferably the foregoing method (1) in which the pressure-sensitive adhesive composition is cured by irradiation with UV rays.
In the coating process in the method of manufacturing the pressure-sensitive adhesive sheet of the present invention, conventional coating methods are applicable, and conventional coaters such as a gravure roll coater, a reverse roll coater, a kiss roll coater, a dip roll coater, a bar coater, a knife coater, a spray coater, a comma coater and a direct coater, can be used.
The thickness (total thickness) of the pressure-sensitive adhesive sheet of the present invention is not particularly limited, but is preferably from 10 μm to 1 mm, more preferably from 100 μM to 500 μm, further preferably from 150 μM to 350 μm. By adjusting the thickness to 10 μm or more, the pressure-sensitive adhesive sheet easily follows step-difference portions, and step absorbability is enhanced. The thickness of the pressure-sensitive adhesive sheet of the present invention is defined as a thickness from a point of the pressure-sensitive adhesive surface on one side of the pressure-sensitive adhesive sheet of the present invention to a point of the pressure-sensitive adhesive surface on the other side. The definition of the thickness of the pressure-sensitive adhesive sheet of the present invention does not include the thickness of the separator.
It is preferable that the pressure-sensitive adhesive sheet of the present invention has high transparency. The haze (in conformity with JIS K 7136) of the pressure-sensitive adhesive sheet of the present invention is preferably 2% or less, more preferably 1% or less. By controlling the haze to 2% or less, an optical products or optical members, which are prepared by laminating via the pressure-sensitive adhesive sheet, can have good transparency and appearance. The total light transmittance (total light transmittance in the visible light wavelength region, which is in conformity with JIS K 7361-1) is not particularly limited, but is preferably 85% or more, more preferably 90% or more. By adjusting the total light transmittance to 85% or more, an optical products or optical members, which are prepared by laminating via the pressure-sensitive adhesive sheet, can have good transparency and appearance. The haze and total light transmittance measurements can be measured by, e.g. laminating the pressure-sensitive adhesive sheet to a glass sheet or the like, and using a haze meter. Specifically, the haze and the total light transmittance can be determined by the method described later in the section “Evaluations” under “(2) Haze and total light transmittance”.
A 180° peeling pressure-sensitive adhesive force (180° peeling pressure-sensitive adhesive force to glass, tensile speed: 300 mm/min, temperature: 23° C.) of the pressure-sensitive adhesive sheet of the present invention at room temperature (23° C.) is not particular limited, but is preferably 5.0 N/20 mm or more (e.g. 5.0 to 50 N/20 mm), more preferably 7.0 N/20 mm or more (e.g. 7.0 to 40 N/20 mm), further preferably 10 N/20 mm or more (e.g. 10 to 30 N/20 mm). If the pressure-sensitive adhesive sheet of the present invention is a double-sided pressure-sensitive adhesive sheet, it is preferable that the pressure-sensitive adhesive surface on at least one side thereof has the 180° peeling pressure-sensitive adhesive force at room temperature (23° C.) which falls within the range specified above, and it is more preferable that the pressure-sensitive adhesive surfaces on both sides thereof have the 180° peeling pressure-sensitive adhesive forces which fall within the range specified above. The 180° peeling pressure-sensitive adhesive force can be measured according to the method described later in the section “Evaluations” under “(6-1) 180° peeling pressure-sensitive adhesive force to glass”.
A 180° peeling pressure-sensitive adhesive force (180° peeling pressure-sensitive adhesive force to polarizing plate, tensile speed: 300 mm/min, temperature: 23° C.) of the pressure-sensitive adhesive sheet of the present invention at room temperature (23° C.) is not particular limited, but is preferably 4.0 N/20 mm or more (e.g. 4.0 to 50 N/20 mm), more preferably 6.0 N/20 mm or more (e.g. 6.0 to 40 N/20 mm), further preferably 8.0 N/20 mm or more (e.g. 8.0 to 30 N/20 mm). If the pressure-sensitive adhesive sheet of the present invention is a double-sided pressure-sensitive adhesive sheet, it is preferable that the pressure-sensitive adhesive surface on at least one side thereof has the 180° peeling pressure-sensitive adhesive force at room temperature (23° C.) which falls within the range specified above, and it is more preferable that the pressure-sensitive adhesive surfaces on both sides thereof have the 180° peeling pressure-sensitive adhesive forces which fall within the range specified above. The 180° peeling pressure-sensitive adhesive force can be measured according to the method described later in the “Evaluations” under “(6-2) 180° peeling pressure-sensitive adhesive force to polarizing plate”.
The pressure-sensitive adhesive sheet of the present invention is preferably a double-sided pressure-sensitive adhesive sheet which satisfies the following: in the following <Peel test at −30° C.> using an adherend A and an adherend B, at least one of the adherend A and the adherend B are damaged; and in the following <Peel test at −50° C.> using the adherend A and the adherend B, the adherend A and the adherend B can be peeled without damaging both of the adherend A and adhrend B.
<Peel test at −30° C.>
A sample piece having a structure of adherend A/double-sided pressure-sensitive adhesive sheet/adherend B is prepared by laminating one pressure-sensitive adhesive surface of a double-sided pressure-sensitive adhesive sheet (size: 30 mm length×26 mm width) to a surface of the following adherend A and laminating the other pressure-sensitive adhesive surface to a surface of the following adherend B. Next, the sample piece is put in an autoclave, and the sample piece is treated for 15 minutes under the conditions of a pressure of 5 atm and a temperature of 50° C., followed by allowing to stand for 30 minutes at a temperature of −30° C. Then, in an environment of −30° C., the adherend A is fixed, and the adherend A and the adherend B are peeled by pulling the adherend B in a direction perpendicular to the surface of the adherend A. The pulling speed during pulling the adherend B is preferably from 10 to 1,000 mm/min, more preferably from 100 to 500 mm/min. The adherend A is a glass sheet (a product of Matsunami Glass Ind., Ltd.; thickness: 0.7 mm, size: 100 mm length×50 mm width). The adherend B is a slide glass, “S1112” (trade name, a product of Matsunami Glass Ind., Ltd.; thickness: 1.0 to 1.3 mm, size: length 76 mm×width 26 mm). More specifically, the testing is carried out according to the method described later in the section “Evaluations” under “(3) Glass/glass reworkability”.
A sample piece having a structure of adherend A/double-sided pressure-sensitive adhesive sheet/adherend B is prepared by laminating one pressure-sensitive adhesive surface of a double-sided pressure-sensitive adhesive sheet (size: 30 mm length×26 mm width) to a surface of the following adherend A and laminating the other pressure-sensitive adhesive surface to a surface of the following adherend B. Next, the sample piece is put in an autoclave, and the sample piece is treated for 15 minutes under the conditions of a pressure of 5 atm and a temperature of 50° C., followed by allowing to stand for 30 minutes at a temperature of −50° C. Then, in an environment of −50° C., the adherend A is fixed, and the adherend A and the adherend B are peeled by pulling the adherend B in a direction perpendicular to the surface of the adherend A. The pulling speed during pulling the adherend B is preferably from 10 to 1,000 mm/min, more preferably from 100 to 500 mm/min. The adherend A is a glass sheet (a product of Matsunami Glass Ind., Ltd.; thickness: 0.7 mm, size: 100 mm length×50 mm width). The adherend B is a slide glass, “S1112” (trade name, a product of Matsunami Glass Ind., Ltd.; thickness: 1.0 to 1.3 mm, size: length 76 mm×width 26 mm). More specifically, the testing is carried out according to the method described later in the “Evaluations” under “(3) Glass/glass reworkability”.
The pressure-sensitive adhesive force at −30° C. of the pressure-sensitive adhesive sheet of the present invention in the following <Film T-peel test> is not particular limited, but is preferably from 5N to 50N, more preferably from 6N to 40N, further preferably from 7N to 35N. By giving the pressure-sensitive adhesive force at −30° C. of 5N or more, the pressure-sensitive adhesive sheet is less prone to be peeled away from an adherend even at −30° C. The pressure-sensitive adhesive force at −50° C. of the pressure-sensitive adhesive sheet of the present invention in the following <Film T-peel test> is not particular limited, but is preferably from 0 to 3N, more preferably from 0 to 2.5N, further preferably from 0 to 2N. By giving the pressure-sensitive adhesive force at −50° C. of 3N or less, the adherend is peeled from the pressure-sensitive adhesive sheet at −50° C.
It is preferable that the pressure-sensitive adhesive sheet of the present invention has the pressure-sensitive adhesive force at −30° C. in a range of from 5N to 50N (preferably from 6N to 40N, more preferably from 7 to 35N) in the following <Film T-peel test>, and has the pressure-sensitive adhesive force at −50° C. in a range of from 0 to 3N (preferably from 0 to 2.5N, more preferably from 0 to 2N) in the following <Film T-peel test>. By adjusting the pressure-sensitive adhesive force as determined in the following <Film T-peel test> to fall within the forgoing ranges, the pressure-sensitive adhesive sheet has the pressure-sensitive adhesive property even at −30° C., and the pressure-sensitive adhesive force is decreased at −40° C. or less (especially −50° C. or less) to make it possible to peel the adherend away without bending the adherend even when the adherend is a warp-prone member such as a film.
A sample piece having a structure of PET film/double-sided pressure-sensitive adhesive sheet/PET film is prepared by laminating one pressure-sensitive adhesive surface of a double-sided pressure-sensitive adhesive sheet (size: 50 mm length×20 mm width, thickness: 175 μm or 150 μm) to a surface of polyethylene tetraphthalate (PET) film (size: 150 mm length×20 mm width×100 μm thickness) and laminating the other pressure-sensitive adhesive surface to a surface of PET film (size: 150 mm length×20 mm width×100 μm thickness). Next, the sample piece is put in an autoclave, and the sample piece is treated for 15 minutes under the conditions of a pressure of 5 atm and a temperature of 50° C., followed by allowing to stand for 30 minutes at either of a temperature of −30° C. or a temperature of −50° C. Then, in the same temperature environment as chosen when the sample piece is stand, a T-peel test is carried out under the following conditions, and the peel strength (N) is determined. More specifically, the testing is carried out according to the method described later in the section “Evaluations” under “(4) Film T-peel test”.
Device: AUTOGRAPH, trade name, manufactured by Shimadzu Corporation
Sample width: 20 mm
Tensile speed: 300 mm/min
Pulling direction: CD direction (direction perpendicular to length (MD) direction)
Number of repetitions: n=3
The pressure-sensitive adhesive sheet of the present invention has excellent pressure-sensitive adhesive property at temperatures ranging from about −30° C. to room temperature (23° C.), and has reworkability at a temperature on the order of −50° C. Even in the case where adherends are laminated by the use of the pressure-sensitive adhesive sheet of the present invention, and then, the adherents are peeled again (removed), the pressure-sensitive adhesive sheet of the present invention can be suitably used as a pressure-sensitive adhesive sheet (removable pressure-sensitive adhesive sheet) having removability which allows reuse of the adherends which has been peeled away.
The use of the pressure-sensitive adhesive sheet of the present invention is not particularly limited, and can be suitably used for optical uses, bonding uses and protection uses. In particular, the pressure-sensitive adhesive sheet of the present invention is preferably a pressure-sensitive adhesive sheet for optical uses (an optical pressure-sensitive adhesive sheet). More specifically, the pressure-sensitive adhesive sheet is a pressure-sensitive adhesive sheet used for the purpose of, e.g. laminating optical members (for lamination of optical members) or manufacturing products (optical products) using optical members.
The optical members are not particular limited so long as they have optical properties (such as a light-polarizing property, a light-refracting property, a light-scattering property, a light-reflecting property, a light-transmitting property, a light-absorbing property, a light-diffracting property, optical rotatory properties and visibility), and examples thereof include members included in optical products, such as display devices (image display devices) or input devices, or members used in these devices (optical products). More specifically, examples thereof include a polarizing plate, a wave plate, a retardation plate, an optical compensation film, a brightness-enhancing film, a light-guiding plate, a reflective film, an anti-reflective film, a transparent conductive film (such as an ITO film), a design film, a decorative film, a surface-protecting film, a prism, a lens, a color filter, a transparent substrate, and various laminates of these members.
Examples of the display devices (image display devices) include liquid-crystal display devices, organic EL (electroluminescent) display devices, PDPs (plasma display panels) and electronic papers. Examples of the input devices include touch panels.
The optical members is not particularly limited, and examples thereof include members (e.g. in a sheet form, film form or plate form) made from plastic materials, such as polyester resins such as polyethylene terephthalate (PET), acrylic resins such as polymethyl methacrylate, polycarbonate, triacetyl cellulose, polysulfone, polyarylate, polyimide, polyvinyl chloride, polyvinyl acetate, polyethylene, polypropylene and ethylene-propylene copolymer, or glass, or metal. The term “optical member” used herein is intended to include, as mentioned above, members (e.g. a design film, a decorative film, a surface protective plate or the like) which play a role of decoration or protection while keeping the visibility of adherends such as display devices or input devices.
The pressure-sensitive adhesive sheet of the present invention has the pressure-sensitive adhesive properties in a wide temperature range of −30° C. to room temperature (23° C.). In addition, the pressure-sensitive adhesive sheet can be peeled away at temperatures on the order of −50° C. or less without exerting a strong force on the member to which the pressure-sensitive adhesive sheet has been laminated. Thus, even when it is a warp-prone member (e.g. a film-shaped member made from a plastic material), the member can be peeled off without bending. Thus, it is preferred that the pressure-sensitive adhesive sheet of the present invention be an optical pressure-sensitive adhesive sheet used for lamination of a plastic-based optical member provided with a break-prone film such as an ITO film (e.g. a transparent conductive film). In addition, the pressure-sensitive adhesive sheet of the present invention can be peeled away even a member which is apt to fracture by a force applied thereto (e.g. an optical member having a high stiffness such as an optical member composed of glass) without causing fracture. Thus, it is also preferred that the pressure-sensitive adhesive sheet of the present invention be an optical pressure-sensitive adhesive sheet used for lamination of an optical member composed of glass, such as a glass sensor, a display panel made from glass (e.g. LCD) or a glass sheet with a transparent electrode in a touch panel.
The method of separating members (e.g. optical members) laminated via the pressure-sensitive adhesive sheet of the present invention is not particularly limited, and examples thereof include a method of separating members laminated via the pressure-sensitive adhesive sheet by exerting a force on at least one of the members in at least the direction of the normal to the member (e.g., a method of separation through the application of a force by inserting the tip of a tool with a cuneiform from the side of the pressure-sensitive adhesive sheet), a method of separating members laminated via the pressure-sensitive adhesive sheet by pulling them in the thickness direction (a method of separation by pulling them in the direction perpendicular to the interface between the pressure-sensitive adhesive sheet and the member), a method of separation by bringing two members laminated into relative movements in parallel with each other, and a method of making at least one of members laminated move so that mutually-parallel virtual straight lines specified in the interface between one member and the pressure-sensitive adhesive sheet and the interface between the other member and the pressure-sensitive adhesive sheet, respectively, come to have a skew positional relationship (a method of making at least one of two members move so that one pressure-sensitive adhesive surface of the pressure-sensitive adhesive sheet is skewed to the other pressure-sensitive adhesive surface of the pressure-sensitive adhesive sheet).
The expression of “bringing two members into relative movements in parallel with each other” as used above implies that at least one of two members laminated via the pressure-sensitive adhesive sheet of the present invention is moved while keeping the distance between opposed surfaces of the two members substantially constant. For instance, when the two members are flat-plate members, the expression means that at least one of two members are moved while holding the parallel relationship between the two members (flat plates).
According to the separation methods as recited above, two members laminated via the pressure-sensitive adhesive sheet of the present invention can be separated without substantially applying thereto such a force (load) as to cause damaging, cracking or distortion (deformation) in the members, even when at least one of the members is a warp-prone member or a thin member having poor flexibility.
The present invention will now be described in further detail by reference to examples and comparative example. However, these examples should not be construed as limiting the scope of the present invention in any way. A composition (kinds and amounts used) of monomers constituting the monomer components and a composition (kinds and amounts used) of ingredients in the pressure-sensitive adhesive composition, which are adopted in each of the following examples and comparative example, are shown in Table 1.
Into a four necked flask, a mixture of 75 parts by weight of lauryl acrylate (LA), 13 parts by weight of isobornyl acrylate (IBXA), 6 parts by weight of N-vinyl-2-pyrrolidone (NVP) and 6 parts by weight of 2-hydroxyethyl acrylate (HEA), and 0.05 parts by weight of 1-hydroxycyclohexyl phenyl ketone (IRGACURE 184, trade name, a product of BASF Japan Ltd.) and 0.05 parts by weight of 2,2-dimethoxy-1,2-diphenylethane-1-one (IRGACURE 651, trade name, a product of BASF Japan Ltd.) as a photopolymerization initiator were added. The resulting mixture was irradiated with UV rays in an atmosphere of nitrogen until the viscosity thereof reached about 15 Pa·s (as measured with a BH viscometer, No. 5 rotor, 10 rpm, temperature of 30° C.), thereby undergoing photo polymerization to yield a partially polymerized monomer syrup (a partial polymerization product of the monomer components).
100 parts by weight of the partially polymerized monomer syrup, 0.035 parts by weight of 1,6-hexanediol diacrylate (HDDA, polyfuntional monomer), 0.3 parts by weight of a silane coupling agent (KBM403, trade name, a product of Shin-Etsu Chemical Co., Ltd.), 0.05 parts by weight of 1-hydroxycyclohexyl phenyl ketone (IRGACURE 184, trade name, a product of BASF Japan Ltd.) as photo polymerization initiator (supplementary initiator) and 0.05 parts by weight of 2,2-dimethoxy-1,2-diphenylethane-1-one (IRGACURE 651, trade name, a product of BASF Japan Ltd.) as photo polymerization initiator (supplementary initiator) were mixed homogeneously, thereby preparing a pressure-sensitive adhesive composition.
The thus prepared pressure-sensitive adhesive composition was applied to the release-treated surface of a release film (MRF#38, trade name, a product of Mitsubishi Plastics, Inc.) so as to have a thickness of 175 μm, thereby forming a pressure-sensitive adhesive composition layer. Subsequently, the other surface of the pressure-sensitive adhesive composition layer was laminated to the release-treated surface of a release film (MRN#38, trade name, a product of Mitsubishi Plastics, Inc.), and the laminate thus formed was subjected to photo-curing through irradiation with UV rays under the conditions of an illumination of 4 mW/cm2 and a light intensity of 1,200 mJ/cm2, thereby forming a pressure-sensitive adhesive layer, and then, a pressure-sensitive adhesive sheet was prepared.
The pressure-sensitive adhesive compositions and pressure-sensitive adhesive sheets were prepared in the same manner as in Example 1, except the change of the kinds and mixing amounts of the monomer components and the kinds and mixing amounts of ingredients in the pressure-sensitive adhesive composition to those as shown in Table 1.
An oligomer A used in each of Examples 3, 5, 7 and 14 was prepared in the following manner.
Into a four necked flask, 60 parts by weight of dicyclopentanyl methacrylate (DCPMA) (dicyclopentanyl methacrylate) (FA-513M, trade name, a product of Hitachi Chemical Co., Ltd.) and 40 parts by weight of methyl methacrylate (MMA) as the monomer components, 3.5 parts by weight of α-thioglycerol as a chain transfer agent, and 100 parts by weight of ethyl acetate as a solvent for polymerization were added. In an atmosphere of nitrogen, these ingredients were stirred for one hour at 70° C., and then, 0.2 parts by weight of 2,2′-zobisisobutyronitrile as a polymerization initiator was added thereto, thereby conducting the reaction at 70° C. for 2 hours, followed by the further reaction at 80° C. for 2 hours. Then, the reaction solution was introduced into an atmosphere of 130° C., and ethyl acetate, the chain transfer agent and the monomers remaining unreacted were removed therefrom by drying. Thus, an oligomer A in a solid form was obtained. The weight-average molecular weight of the oligomer A was 4,000. In addition, the glass transition temperature (Tg) of the oligomer A was 130° C.
Into a four necked flask, a mixture of 73 parts by weight of lauryl acrylate (LA), 21 parts by weight of N-vinyl-2-pyrrolidone (NVP) and 6 parts by weight of 2-hydroxyethyl acrylate (HEA), and 0.1 parts by weight of 1-hydroxycyclohexyl phenyl ketone (IRGACURE 184, trade name, a product of BASF Japan Ltd.) and 0.1 parts by weight of 2,2-dimethoxy-1,2-diphenylethane-1-one (IRGACURE 651, trade name, a product of BASF Japan Ltd.) were added. The resulting mixture was irradiated with UV rays in an atmosphere of nitrogen until the viscosity thereof reached about 15 Pa·s (as measured with a BH viscometer, No. 5 rotor, 10 rpm, temperature of 30° C.), thereby undergoing photo polymerization to yield a partially polymerized monomer syrup (a partial polymerization product of the monomer components).
100 parts by weight of the partially polymerized monomer syrup, 0.01 parts by weight of 1,6-hexanediol diacrylate (HDDA, polyfuntional monomer), 0.5 parts by weight of dimethylaminoethyl acrylate (DMAEA, tertiary amino group-containing monomer) and 0.3 parts by weight of a silane coupling agent (KBM403, trade name, a product of Shin-Etsu Chemical Co., Ltd.) were mixed homogeneously, thereby preparing a pressure-sensitive adhesive composition.
The thus prepared pressure-sensitive adhesive composition was applied to the release-treated surface of a release film (MRF#38, trade name, a product of Mitsubishi Plastics, Inc.) so as to have a thickness of 150 μm, thereby forming a pressure-sensitive adhesive composition layer. Subsequently, the other surface of the pressure-sensitive adhesive composition layer was laminated to the release-treated surface of a release film (MRN#38, trade name, a product of Mitsubishi Plastics, Inc.), and the laminate thus formed was subjected to photo-curing through irradiation with UV rays under the conditions of an illumination of 4 mW/cm2 and a light intensity of 1,200 mJ/cm2, thereby forming a pressure-sensitive adhesive layer, and thus, a pressure-sensitive adhesive sheet was prepared.
The pressure-sensitive adhesive compositions and pressure-sensitive adhesive sheets were prepared in the same manner as in Example 8, except the change of the kinds and mixing amounts of the monomer components and the kinds and mixing amounts of ingredients in the pressure-sensitive adhesive composition to those as shown in Table 1.
The gel fraction, haze, total light transmittance, glass/glass reworkability, film T-peel test, melting point and 180° peeling pressure-sensitive adhesive force were evaluated for each of the pressure-sensitive adhesive compositions and pressure-sensitive adhesive sheets obtained in Examples and Comparative Example. The methods by which these evaluations were performed are described below. The results of these evaluations are shown in Table 1.
The measurement of the gel fraction was conducted according to the description in the above section “Method of measuring gel fraction”.
From each of the pressure-sensitive adhesive sheets obtained in Examples and Comparative Example, the release film (MRN#38) on one side was peeled away, and the resulting pressure-sensitive adhesive sheet was laminated to a glass sheet (SLIDE GLASS S111, trade name, a product of Matsunami Glass Ind., Ltd.; thickness: 1.0 mm, Haze: 0.1%), and further the release film on the other side was peeled away. Thus, sample pieces were prepared.
On each of these sample pieces, the measurement of the haze (%) in conformity with JIS K 7136 and total light transmittance (%) in conformity with JIS K 7361-1 were conducted by using a haze meter (HM-150, trade name, a product of Murakami Color Research Laboratory).
A sheet piece (size: 30 mm length×26 mm width) was cut from each of the pressure-sensitive adhesive sheets obtained in Examples and Comparative Example. The release film (MRN#38) on one side of the sheet piece was peeled away. The resulting sheet piece was laminated to a slide glass (a) 12, and the release film (MRF#38) on the other side was peeled away, and the other pressure-sensitive adhesive surface was laminated to a glass sheet (b) 13. In this way, the slide glass (a) 12 (size: 76 mm length×26 mm width, thickness: 1.0 mm) and the glass sheet (b) 13 (size: 100 mm length×50 mm width, thickness: 0.7 mm) were laminated via the sheet piece 11, thereby forming an evaluative sample as shown in
Each of the evaluative samples was placed in an autoclave and the evaluative samples were treated for 15 minutes under a pressure of 5 atm and a temperature of 50° C. After the autoclave treatment, each evaluative sample was taken out of the autoclave, and allowed to stand for 30 minutes at a temperature of −30° C. Subsequently, as shown in
The glass/glass reworkability (−30° C.) was rated as “good (A)” when both the slide glass (a) and the glass (b) were separated without breaking, and it was rated as “poor (B)” when at least one of the slide glass (a) and the glass (b) were damaged.
Each of the evaluative samples was placed in an autoclave and the evaluative samples were treated for 15 minutes under a pressure of 5 atm and a temperature of 50° C. After the autoclave treatment, each evaluative sample was taken out of the autoclave, and allowed to stand for 30 minutes at a temperature of −50° C. Subsequently, as shown in
The glass/glass reworkability (−50° C.) was rated as “good (A)” when both the slide glass (a) and the glass (b) were separated without breaking, and it was rated as “poor (B)” when at least one of the slide glass (a) and the glass (b) were damaged.
Sheet pieces (size: 50 mm length×20 mm width, thickness: 175 μm or 150 μm) were cut from each of the pressure-sensitive adhesive sheets obtained in Examples and Comparative Example. The release film (MRN#38) on one side of each sheet piece was peeled away. The resulting sheet piece was laminated to a polyethylene terephthalate film (PET film) (i) 22 (A4100, trade name, a product of TOYOBO CO., LTD., size: 150 mm length×20 mm width, thickness: 100 μm), and the release film (MRF#38) on the other side was peeled away, and the other pressure-sensitive adhesive surface was laminated to a PET film (ii) 23 (A4100, trade name, a product of TOYOBO CO., LTD., size: 150 mm length×20 mm width, thickness: 100 μm), and thus, the PET film (i) 22 and the PET film (ii) 23 were laminated via the sheet piece 21 thereby to form an evaluative sample (
Each of the evaluative samples was placed in an autoclave and the evaluative samples were treated for 15 minutes under a pressure of 5 atm and a temperature of 50° C. After the autoclave treatment, each evaluative sample was taken out of the autoclave, and the sheet pieces thereof were allowed to stand for 30 minutes under the environments of a temperature of −30° C. or −50° C. Thereafter, in the environment same as the environment where the sheet piece was left standing for 30 minutes, one end 24 of the PET film (i) and one end 25 of the PET film (ii) were fixed to a tensile tester by means of chucks (gripping tools), and the end 24 of the PET film (i) was pulled in the pulling direction shown in
Device (Tensile tester): AUTOGRAPH, trade name, a product of Shimadzu Corporation
Sample width: 20 mm
Pulling speed: 300 mm/min
Pulling direction: CD direction (the direction shown by the arrow in
Number of repetitions: n=3
The separability was rated as A (excellent, or equivalently, poor in pressure-sensitive adhesive property) when the film T-peel force measured was less than 2N, it was rated as B (somewhat poor, or equivalently, good in pressure-sensitive adhesive property) when the film T-peel force measured was 2N or more and less than 5N, and it was rated as C (poor, or equivalently, excellent in pressure-sensitive adhesive property) when the film T-peel force measured was 5N or more.
The evaluation results of the film T-peel force in the film T-peel test at −30° C. and the separability are shown in the columns “Film T-peel force (N) (−30° C.)” and “Separability evaluation (−30° C.)” of Table 1, respectively. The evaluation results of the film T-peel force in the film T-peel test at −50° C. and the separability are shown in the columns “Film T-peel force (N) (−50° C.)” and “Separability evaluation (−50° C.)” of Table 1, respectively.
A sample for measurement was prepared by taking 2 to 3 mg of pressure-sensitive adhesive layer out of each of the pressure-sensitive adhesive sheets obtained in Examples and Comparative Example, putting the taken pressure-sensitive adhesive layer in an aluminum container and crimping the container. The sample for measurement was subjected to the measurement using a differential scanning calorimeter (DSC) (Q-2000, trade name, a product of TA Instruments, Inc.) in conformity with JIS K 7121 under the condition of a rate of temperature rise of 10° C./min in the temperature range of from −80° C. to 80° C., and the temperature (Tm) of the heat-absorption peak top in this measurement was defined as a melting point (° C.).
When a sample was not crystallized, the melting point of the sample was not able to be measured. The melting point in this case is symbolized by “x”.
In addition, the case where no measurement for the melting point was made is symbolized by “−”.
A sheet piece having a length of 100 mm and width of 20 mm (a sheet piece having a size of 100 mm×20 mm) was cut from each of the pressure-sensitive adhesive sheets obtained in Examples and Comparative Example. The release film (MRN#38) on one side of the sheet piece was peeled away, and the thus bared pressure-sensitive adhesive surface (surface opposite to the surface to be measured) of the sheet piece was laminated to (lined with) a PET film (LUMIRROR S-10, trade name, a product of TORAY INDUSTRIES, INC., thickness: 50 μm), thereby making a sheet piece in rectangular form.
Subsequently, the release film (MRF#38) on the other side was peeled away from the sheet piece in rectangular form, and the thus bared pressure-sensitive adhesive surface (the surface to be measured) was pressed on a glass sheet (manufactured by Matsunami Glass Ind., Ltd.; thickness: 0.7 mm) by moving a 2 kg roller forward and backward once in the atmosphere of 23° C., thereby making a sample for measurement.
The sample for measurement was allowed to stand for 30 minutes in the atmosphere of 23° C. and 50% RH, and after that, a 180° peel test was carried out using a tensile tester, and then 180° peeling pressure-sensitive adhesive force (N/20 mm) to the glass sheet was measured. This measurement was carried out in the atmosphere of 23° C. and 50% RH under the conditions of a peel angle of 180° and a tensile speed of 300 mm/min.
A sheet piece having a length of 100 mm and a width of 20 mm (a sheet piece having a size of 100 mm×20 mm) was cut from each of the pressure-sensitive adhesive sheets obtained in Examples and Comparative Example. The release film (MRN#38) on one side of the sheet piece was peeled away, and the thus bared pressure-sensitive adhesive surface (surface opposite to the surface to be measured) of the sheet piece was laminated to (lined with) a PET film (LUMIRROR S-10, trade name, a product of TORAY INDUSTRIES, INC., thickness: 50 μm), thereby making a sheet piece in rectangular form.
Subsequently, the release film (MRF#38) on the other side was peeled away from the sheet piece in rectangular form, and the thus bared pressure-sensitive adhesive surface (the surface to be measured) was pressed on a polarizing plate (manufactured by NITTO DENKO CORPORATION; thickness: 250 μm) by moving a 2 kg roller forward and backward once in the atmosphere of 23° C., thereby making a sample for measurement.
The sample for measurement was allowed to stand for 30 minutes in the atmosphere of 23° C. and 50% R11, and after that, a 180° peel test was carried out using a tensile tester, and the 180° peeling pressure-sensitive adhesive force (N/20 mm) to the polarizing plate was measured. This measurement was carried out in the atmosphere of 23° C. and 50% RH under the conditions of a peel angle of 180° and a tensile speed of 300 mm/min.
When such measurement was not made, the mark “−” is shown in the column “180° peeling pressure-sensitive adhesive force to polarizing plate (N/20 mm)”.
A sheet piece having a length of 100 mm and a width of 50 mm (a sheet piece having a size of 100 mm×50 mm) was cut from each of the pressure-sensitive adhesive sheets obtained in Examples and Comparative Example. The release film (MRN#38) on one side of the sheet piece was peeled away, and the thus bared pressure-sensitive adhesive surface of the sheet piece was laminated to a glass sheet (a product of Matsunami Glass Ind., Ltd.; thickness: 0.7 mm, size: 100 mm length×50 mm width) by means of a hand roller. The release film (MRF#38) on the other side was peeled away, and the thus bared pressure-sensitive adhesive surface was also laminated to a glass sheet (a product of Matsunami Glass Ind., Ltd.; thickness: 0.7 mm, size: 100 mm length×50 mm width) in the same manner, thereby laminating the two glass sheets via the sheet piece. Thus, evaluative samples having a structure of glass sheet/pressure-sensitive adhesive sheet (sheet piece)/glass sheet were obtained.
Each of the evaluative samples was placed in an autoclave, followed by subjecting to autoclave treatment for 15 minutes under a pressure of 5 atm and a temperature of 50° C. After the autoclave treatment, each evaluative sample was taken out of the autoclave, followed by allowing to stand for 100 hours in humidified environments (temperature: 85° C., humidity: 85% RH). Then, each evaluative sample was allowed to stand for 24 hours in room temperature environments (temperature: 23° C., humidity: 50% RH). Thereafter, whether or not white turbidity developed in the pressure-sensitive adhesive layer of each evaluative sample was visually observed, and evaluated on the basis of the following criteria.
In white turbidity resistance under humidified conditions, the case where no white turbidity was observed was rated as A (excellent), the case where white turbidity was observed in the pressure-sensitive adhesive only at the four corners of the evaluative sample was rated as B (good), and the case where white turbidity was observed over the whole pressure-sensitive adhesive in the evaluative sample was rated as C (poor).
As can be clearly seen from the results shown in Table 1, the pressure-sensitive adhesive sheets prepared in Examples 1 to 14 had excellent pressure-sensitive adhesive properties at room temperature, and had excellent pressure-sensitive adhesive properties at −30° C. In addition, they had excellent reworkability at −50° C. Further, the pressure-sensitive adhesive sheets prepared in Examples 4 to 14 were especially superior in white-turbidity resistance under humidified conditions. Furthermore, the pressure-sensitive adhesive sheets prepared in Examples 8 to 14 were especially superior in pressure-sensitive adhesive force to polarizing plates.
While the invention has been described in detail and with reference to specific embodiments thereof, it will be apparent to one skilled in the art that various changes and modifications can be made therein without departing from the spirit and scope thereof
This application is based on Japanese Patent Application No. 2013-46768 filed on Mar. 8, 2013, the entire subject matters of which are incorporated herein by reference.
