TW201402763A - Adhesive tape - Google Patents

Abstract

An adhesive tape comprising an adhesive layer on a foam backing, wherein the foam backing has a thickness of 250 μ m or less and interlayer strength of 10 to 18 N/cm, and the adhesive layer has a thickness of 40 μ m or less and properties such that when an adhesive tape formed by providing an adhesive layer with a thickness of 25 μ m on a PET backing with a thickness of 25 μ m is bonded to an SUS plate by compression in a single back and forth motion with a 2 kg roller in an environment including a temperature of 23 DEG C and a relative humidity of 65% RH, and subsequently left to stand for one hour in an environment having a temperature of 23 DEG C and relative humidity of 50% RH, the adhesive tape exhibits a 180 DEG peeling adhesive strength of 0.6 to 2 N/25 mm at a peel rate of 300 mm/min. Such an adhesive tape is suitable for securing an organic EL display, and can realize excellent shock resistance and favorable reworkability despite its thin profile.

Description

Adhesive tape

The present invention relates to an adhesive tape using a foam substrate.

With the thinning of mobile electronic devices such as electronic notebooks, mobile phones, PHS, digital cameras, music players, televisions, tablet PCs, notebook PCs, and game consoles in recent years, image display of such mobile electronic devices When the device is used with an organic EL (Electro Luminescence) display, when the organic EL display and the panel for protecting the image display unit are bonded, and the organic EL display such as the organic EL display and the housing, and the like, and the support inside the mobile electronic device, etc. Use adhesive tape.

As an adhesive tape for fixing a component of a mobile electronic device, for example, a sticky tape having a soft foam as a base material has been disclosed (see Patent Documents 1 and 2), and these adhesive tapes are thin and have good followability. It is ideal to use parts that are fixed in mobile electronic devices.

When the parts of the mobile electronic device are fixed, it is easy to be impacted by the drop, so the desired impact resistance is required. In particular, the organic EL display is extremely thin, and the glass plate used here is also a very thin glass plate, so high impact resistance is required. Sex. Furthermore, organic EL displays are expensive, and when the parts are fixed and the mobile electronic devices after manufacture are defective, it is also necessary to be able to separate the fixed organic displays ideally. In particular, when the organic EL display is bonded to a plate-like rigid body member such as a support or a frame of a mobile electronic device, the plate-like rigid member is bonded to each other, and the thin organic EL display is likely to be damaged during rework, so it is necessary High workability. Accompanied by action electronics The large screen of the device or the increase of the touch panel, the fixing tape of the organic EL display also needs to maintain the force in the cutting direction.

[Patent Document 1] Japanese Patent Laid-Open Publication No. 2010-155969

[Patent Document 2] Japanese Patent Laid-Open Publication No. 2010-260880

An object of the present invention is to provide an adhesive tape which is capable of ideally fixing an organic EL display, which is thin and has good impact resistance and excellent workability.

In the present invention, it has been found that the organic EL display can be ideally fixed by using the following adhesive tape, and the thin impact can achieve excellent impact resistance and excellent workability, and the above problem is solved: the adhesive tape is used. Fixed to the organic EL display, The adhesive base material has an adhesive layer on at least one side of the foam base material, and the foam base material has a thickness of 250 μm or less and an interlayer strength of 10 to 18 N/cm, and the adhesive layer has a thickness of 40 μm or less and will be A PET substrate having a thickness of 25 μm is formed by providing an adhesive layer with a thickness of 25 μm in an environment of a temperature of 23° C. and a relative humidity of 65% RH, using a 2 kg roller to crimp the SUS plate one by one with a number of crimping times, and After standing for 1 hour in an environment of a temperature of 23 ° C and a relative humidity of 50% RH, the peeling adhesion force at a peeling speed of 300 mm/min of 180 degrees was 0.6 to 2 N/25 mm.

Since the adhesive tape of the present invention is thin and excellent in impact resistance when dropped, it is possible to achieve desired impact resistance even when a breakable organic EL display is applied to a mobile electronic device which is susceptible to drop impact. Moreover, since the organic EL display can be ideally fixed and has good reworkability, even if a defect occurs, the components of the mobile electronic device can be separated with good efficiency. Further, when a force in the shearing direction is applied to the organic EL display, the organic EL display can be desirably prevented from falling off, and the organic EL display can be desirably fixed. Therefore, the organic EL of the present invention The adhesive tape for fixing the display is suitable for fixing an organic EL display using a mobile EL such as a smart phone or a tablet type personal computer, a notebook type personal computer, a game machine, or the like. In particular, even when the protective member of the image display unit or the rigid member such as the plate-like frame of the bonding unit and the plate-shaped support inside the mobile electronic device is fixed to the organic EL display, ideal adhesion or impact resistance can be achieved. It is excellent in the ability to achieve excellent workability, so it is particularly suitable for fixing between these plate-like rigid body members and organic EL displays.

1‧‧‧Adhesive tape

2‧‧‧Acrylic sheet

3‧‧‧ABS board

4‧‧‧ inverted font type measuring platform

5‧‧‧ shot core

6‧‧‧Adhesive tape

7‧‧‧Aluminum foil (substrate material)

8‧‧‧SUS board

9‧‧‧ Loads

Fig. 1 is a conceptual view showing a test piece used in the test for impact resistance test from the top surface.

Fig. 2 is a conceptual view showing a test piece used in the test for impact resistance test from the top surface.

Figure 3 shows a conceptual diagram of the test method for the impact resistance test.

Figure 4 shows a conceptual diagram of the test method for shear retention.

The adhesive tape of the present invention has an adhesive layer on at least one side of the foam base material, and the foam base material has a thickness of 250 μm or less and an interlayer strength of 10 to 18 N/cm. Further, the pressure-sensitive adhesive layer has a thickness of 40 μm or less, and an adhesive tape formed by providing an adhesive layer having a thickness of 25 μm on a PET substrate having a thickness of 25 μm is used in an environment of a temperature of 23° C. and a relative humidity of 65% RH. The SUS plate was pressure-bonded one time after the number of crimping, and was allowed to stand for 1 hour in an environment of a temperature of 23 ° C and a relative humidity of 50% RH, and a peeling force of 0.6 to 2 N at a peeling speed of 300 mm/min. 20mm.

[Foam substrate]

The foam substrate used in the present invention has a thickness of 250 μm or less, preferably 50 to 250 μm, more preferably 80 to 200 μm. By this thickness, although the thin shape can maintain the adhesion to the adherend and at the same time suppress the elongation of the foam substrate, good reworkability can be achieved even when the easily rupturable organic EL display is peeled off.

Further, the foam substrate used in the present invention has an interlayer strength of 10 to 18 N/cm, preferably 12 to 16 N/cm. By setting the interlaminar strength to this range, it is easy to ensure good adhesion to the adherend and excellent impact resistance. Furthermore, when the adhered organic EL display is peeled off in order to improve the productivity of the mobile electronic device, or when the adhered organic EL display is separated, decomposed, and disassembled in order to repair or regenerate or reuse the finished product, Can give good reworkability.

The above interlayer strength can be measured by the following method. On both sides of the foam base material for evaluating the interlayer strength, each of the adhesive layers having a thickness of 50 μm adhered to the adhesive layer (which is not peeled off from the adherend and the foam substrate in the following high-speed peeling test) is attached. The mixture was aged at 40 ° C for 48 hours to prepare a double-sided adhesive tape for measuring the interlayer strength. Then, the adhesive surface of one side was passed through a double-sided adhesive tape sample having a width of 1 cm and a length of 15 cm (flow direction and width direction of the foam substrate) of a polyester film substrate having a thickness of 25 μm, at 23 ° C, 50% RH. The polyester film was bonded to a thickness of 50 μm, a width of 3 cm, and a length of 20 cm by a 2 kg roller back and forth, and allowed to stand at 60 ° C for 48 hours. After standing at 23 ° C for 24 hours, the side bonded to the polyester film having a thickness of 50 μm was fixed to a mounting jig of a high-speed peeling test machine at 23 ° C and 50% RH, and the polyester film having a thickness of 25 μm was measured. The stretching speed is 15 m/min and stretched in the direction of 90 degrees until the maximum strength of the foam is broken.

The 25% compressive strength of the foam substrate used in the present invention is preferably 30 kPa or more, more preferably 30 to 450 kPa, and particularly preferably 50 to 120 kPa. If the foam base material has a 25% compression strength in this range, it is easy to obtain a more suitable workability of the organic EL display.

Further, the 25% compressive strength was measured in accordance with JIS K6767. The sample cut into 25 mm square was superposed to a thickness of about 10 mm. The sample was sandwiched between stainless steel plates having an area larger than the sample, and the strength at which the sample was compressed to about 2.5 mm (25% of the original thickness) was measured at 23 ° C at a speed of 10 mm/min.

The density of the foam substrate is preferably 0.1 to 0.7 g/cm ^{3 , more} preferably 0.1 to 0.5 g/cm ^{3 , and} even more preferably 0.15 to 0.45 g/cm ³ . If it is this density, even if it is the thickness of the said thin form, it is easy to achieve the favorable followability and adhesiveness, and the outstanding workability. In addition, this density is an apparent density measured by JIS K6767, and is obtained by measuring the mass of a foam base material cut into a rectangular shape of 4 cm × 5 cm by a weight of about 15 cm ³ .

The average bubble diameter in the flow direction and the width direction of the foam substrate used in the present invention is not particularly limited, and is preferably adjusted in the range of 10 to 700 μm, more preferably 30 to 500 μm, and more preferably 50 to 400 μm. When the average cell diameter in the flow direction and the width direction is within this range, it is easy to ensure adhesion to the adherend, and it is easy to improve impact resistance. Moreover, it is easy to ensure independent bubbles existing in a unit width.

Further, the ratio of the average bubble diameter in the flow direction to the width direction is not particularly limited, and when the flow direction is 1, it is preferably 0.25 to 4 times, more preferably 0.33 to 3 times, still more preferably 0.6 to 1.5 times, and particularly preferably 0.7 to 1.3 times. In the above ratio range, the softness or tensile strength of the flow direction of the foam substrate and the width direction are less likely to be uneven.

The average cell diameter in the thickness direction of the foam substrate used in the present invention is preferably from 10 to 100 μm, more preferably from 15 to 60 μm. When the average cell diameter in the predetermined thickness direction is within this range, the adhesive tape of the thin type as described above can achieve satisfactory followability and cushioning properties, and the adhesion between the organic EL display and the rigid member can easily achieve excellent adhesion. In addition, it is preferable that the average cell diameter in the thickness direction is 1/2 or less, preferably 1/3 or less, of the thickness of the foam substrate, and it is preferable to secure the density or strength of the foam substrate.

The ratio of the average cell diameter of the foam substrate to the average cell diameter in the thickness direction of the foam substrate (average cell diameter in the flow direction/average cell diameter in the thickness direction), and the width of the foam substrate The ratio of the average bubble diameter in the direction to the average bubble diameter in the thickness direction of the foam substrate (average bubble diameter in the width direction/average bubble diameter in the thickness direction) is preferably 1 to 15, more preferably 1.5 to 10, more preferably 2~8. By this ratio, it is easy to improve the durability against the breakage of the foam layer at the time of the impact of the drop, and it is easy to ensure good followability and cushioning property in the thickness direction, and the bonding between the organic EL display and the rigid body member is easily prevented from occurring. Good adhesion to the gap in which water can enter.

In terms of the bubble size in the foam substrate, the average bubble volume calculated from the average bubble diameter is preferably 50 to 150 μm, more preferably 70 to 120 μm, in terms of the bubble being a true ball.

Further, the average bubble diameter of the foam substrate in the width direction, the flow direction, and the thickness direction was measured in the following manner. First, the foam substrate was cut into 1 cm in the width direction and in the flow direction. Then, the central portion of the cut surface of the cut foam substrate was magnified 200 times by a digital microscope (trade name "KH-7700", manufactured by HiROX Co., Ltd.), and then the foam base was obtained. The cut surface of the material was observed in the width direction of the foam substrate or the cross section of the flow direction in the thickness direction of the substrate. On the obtained enlarged image, the bubble diameter of all the bubbles existing on the cut surface having an actual length of 2 mm before the flow direction or the width direction was measured, and the average bubble diameter was calculated from the average value thereof. The average bubble diameter was obtained from the results measured at any of the 10 points.

The bubble structure of the foam substrate used in the present invention is preferably a closed cell structure, and it is effective to prevent water from seeping from the cut surface of the foam substrate. The shape of the bubble forming the closed cell structure is such that it has a moderate follow-up property and a cushioning property by forming an independent bubble having a shape in the flow direction or the width direction, or an average bubble diameter of both of which is longer than the average bubble diameter in the thickness direction of the foam. More ideal.

Use of the foam substrate of the present invention, the flow of the tensile strength in the width direction is not particularly limited, each of 300N / cm ² or more preferred, more preferably 400 ~ 1200N / cm ^2. Further, the tensile elongation at the time of cutting in the tensile test is not particularly limited, and the tensile elongation in the flow direction is preferably from 100 to 1200%, more preferably from 200 to 1,000%, still more preferably from 200 to 600%. By the foam base material having a tensile strength or a tensile elongation within this range, the processability of the adhesive tape can be prevented from deteriorating or the adhesion property can be lowered even if it is a foamed soft base material. Further, when the adhesive tape is peeled off, the interlayer breakage or tear of the foam is less likely to occur, and the adhesive tape can be easily peeled off even if interlayer cracking occurs.

Further, the tensile strength in the flow direction and the width direction of the foam substrate was measured in accordance with JIS K6767. A sample with a length of 2 cm and a width of 1 cm was used, using a TENSILON tensile tester at 23 ° C. The maximum strength measured under the conditions of a tensile speed of 300 mm/min in an environment of 50% RH.

The compressive strength, density, interlayer strength, tensile strength, and the like of the foam base material can be appropriately adjusted depending on the material of the substrate to be used or the foam structure. The type of the foam substrate used in the present invention is not particularly limited as long as the interlayer strength or the like can be achieved, and polyethylene, polypropylene, and B can be used. A polyolefin-based foam composed of an ene-propylene copolymerized polymer, an ethylene-vinyl acetate copolymerized polymer, or the like, a rubber system composed of a polyurethane foam, an acrylic rubber, or another elastomer. In the foamed body, it is preferable that the polyolefin-based foam is preferably a foamed base material having a thin closed-cell structure excellent in followability of the surface of the adherend or unevenness in cushion absorption.

Among the polyolefin-based foams using the polyolefin-based resin, it is preferred to use a polyethylene-based resin, and it is easy to produce a uniform thickness, and it is easy to impart desired flexibility. In particular, the content of the polyethylene resin in the polyolefin tree is preferably 40% by mass or more, more preferably 50% by mass or more, still more preferably 60% by mass or more, and particularly preferably 100% by mass.

In addition, the polyethylene-based resin used as the polyolefin-based foam is a polyethylene-based resin obtained by using a metallocene compound containing a tetravalent transition metal as a polymerization catalyst, and has a narrow molecular weight distribution and is a copolymer. Any of the molecular weight components can be introduced into the copolymer component in substantially equal proportions, and the polyolefin-based foam can be uniformly crosslinked. Therefore, since the foamed sheet is uniformly crosslinked, the foamed sheet is easily extended as needed, and the thickness of the obtained polyolefin-based resin foam is preferably uniform throughout, which is preferable.

In addition, the polyolefin-based resin constituting the polyolefin-based foam may contain a polyolefin-based resin other than the polyethylene-based resin obtained by using a metallocene compound of a tetravalent transition metal as a polymerization catalyst. Examples of such a polyolefin-based resin include polyethylene resins and polypropylene resins other than the above. Further, the polyolefin resin may be used singly or in combination of two or more.

Such a polyethylene-based resin is, for example, a linear low-density polyethylene, a low-density polyethylene, a medium-density polyethylene, a high-density polyethylene, an ethylene-α-olefin copolymer containing 50% by weight or more of ethylene, and an ethylene-containing 50. The ethylene-vinyl acetate copolymer or the like may be used singly or in combination of two or more kinds. An α-olefin constituting an ethylene-α-olefin copolymer, for example, propylene, 1-butene, 1-pentene, 4-methyl-1-pentene, 1-hexene, 1-heptene, 1-octyl Alkene and the like.

In addition, the polypropylene-based resin is not particularly limited, and examples thereof include polypropylene and a propylene-α-olefin copolymer containing 50% by weight or more of propylene. These may be used alone or in combination of two or more. An α-olefin constituting a propylene-α-olefin copolymer, for example, ethylene, 1-butene, 1-pentene, 4-methyl-1-pentene, 1-hexene, 1-heptene, 1-octyl Alkene and the like.

When the polyolefin-based foam is cross-linked, and the foamable polyolefin-based resin sheet is foamed by a thermally decomposable foaming agent, crosslinking is preferred. When the degree of crosslinking is small, when the foam base material is stretched, bubbles in the vicinity of the surface of the foamed sheet may be broken and the surface may be rough, and the adhesion to the acrylic pressure-sensitive adhesive layer may be lowered. When the foaming polyolefin resin composition is heated and foamed, the foamable polyolefin resin composition is less likely to follow the foaming, and the foaming polyolefin resin composition is not likely to be obtained. The crosslinked polyolefin-based resin foamed sheet having a foaming ratio has a poor impact absorbability, and is preferably from 5 to 60% by mass, more preferably from 20 to 55% by mass.

Next, a method of producing a polyolefin resin foam will be described. The method for producing the polyolefin-based resin foam is not particularly limited, and for example, a method comprising the steps of: supplying the foamable polyolefin-based resin composition to an extruder, performing melt-kneading, and extruding into a sheet shape from an extruder The foamable polyolefin-based resin sheet containing a polyethylene obtained by using a metallocene compound containing a tetravalent transition metal of 40% by weight or more as a polymerization catalyst. a resin-based polyolefin resin, a thermally decomposable foaming agent, a foaming aid, a coloring agent for coloring the foam into black or white, and the like; crosslinking the foamable polyolefin resin sheet; The foamable polyolefin-based resin sheet is foamed; the foamed sheet is melted or softened, and is extended in either the flow direction or the width direction in either direction to extend the foam sheet. Further, the step of extending the foamed sheet may be carried out as needed, and may be carried out a plurality of times.

In addition, a method of crosslinking a polyolefin-based resin foam substrate, for example, a method of irradiating a foamable polyolefin-based resin sheet with ionizing radiation, and pre-blending organic with a foamable polyolefin-based resin composition The peroxide is a method in which the obtained expandable polyolefin-based resin sheet is heated to decompose the organic peroxide, and the like, and these methods may be used in combination.

Examples of the ionizing radiation include an electron beam, an α line, a β line, and a γ line. The amount of the radiation of the ionizing radiation can be appropriately adjusted so that the gel fraction of the polyolefin resin foam base material is in the above-described desired range, but it is preferably in the range of 5 to 200 kGy. Moreover, the irradiation of ionizing radiation is easy to obtain uniform From the viewpoint of the foaming state, it is preferred that the both sides of the foamable polyolefin-based resin sheet are preferably irradiated, and the amount of the radiation irradiated on both sides is preferably the same.

Organic peroxides, for example: 1,1-bis(t-butylperoxy) 3,3,5-trimethylcyclohexane, 1,1-bis(t-butylperoxy)cyclohexane, 2,2-bis(t-butylperoxy)octane, 4,4-bis(t-butylperoxy)-n-butyl valerate, di-tert-butyl peroxide, tert-butylisopropyl Phenyl peroxide, dicumyl peroxide, α,α'-bis(t-butylperoxy-m-isopropyl)benzene, 2,5-dimethyl-2,5-di ( Tert-butyl peroxy)hexane, 2,5-dimethyl-2,5-di(t-butylperoxy)hexyne-3, benzammonium peroxide, cumene peroxynonanoate Ester, tert-butyl peroxybenzoate, 2,5-dimethyl-2,5-bis(benzimidyl peroxy)hexane, butyl peroxydicarbonate, peroxy acrylate The third butyl carbonate or the like may be used singly or in combination of two or more.

When the amount of the organic peroxide added is small, the crosslinking of the foamable polyolefin-based resin sheet may be insufficient. When the amount is large, the obtained crosslinked polyolefin-based resin foam sheet may have an organic peroxide remaining. Since the residue is decomposed, it is preferably 0.01 to 5 parts by weight, more preferably 0.1 to 3 parts by weight, per 100 parts by weight of the polyolefin resin.

The amount of the thermally decomposable foaming agent to be added to the foamable polyolefin resin composition can be appropriately determined depending on the expansion ratio of the polyolefin resin foam substrate, and if it is small, the foamable polyolefin resin sheet is small. The foaming property is lowered, and a polyolefin-based resin foam substrate having a desired expansion ratio may not be obtained. When the polyolefin resin foam substrate is obtained, the tensile strength and compression recovery property of the polyolefin-based resin foam substrate may be obtained. The amount is preferably from 1 to 40 parts by weight, more preferably from 1 to 30 parts by weight, per 100 parts by weight of the polyolefin resin.

Moreover, the method of foaming the foamable polyolefin-based resin sheet is not particularly limited, and for example, a method using hot air heating, a method using infrared heating, a method using a salt bath, a method using an oil bath, or the like may be used in combination. Wait. Among them, the method of heating by hot air or the method of heating by infrared rays is preferable because the difference in surface and back surface is small in terms of the appearance of the surface of the polyolefin resin foam substrate.

The expansion ratio of the foam base material is not particularly limited, and is 2% of the thickness of the thin type, the compressive strength or density, the interlaminar strength, and the like are in the above range, and it is easy to achieve impact resistance or excellent adhesion to the adherend, and rework The view of fitness is 1.5 to 6 times better, 1.8 to 5.5 times better, and more preferably 2.5 to 5 times.

Further, the expansion of the foam base material can be carried out after foaming the foamable polyolefin resin sheet to obtain a foam base material, or by foaming the foamable polyolefin resin sheet. In addition, when the foamed base material sheet is foamed to obtain a foam base material, when the foam base material is stretched, the molten base material can be maintained without cooling the foam base material, and the expansion can be continued. After the foam substrate or the foam substrate is cooled, the foam sheet is heated again to be in a molten or softened state, and the foam substrate is stretched in this state.

Here, the molten state of the foam base material means a state in which the foam base material is heated to a temperature equal to or higher than the melting point of the polyolefin-based resin constituting the foam base material. In addition, the softening of the foam base material means a state in which the foam base material is heated to a temperature at which the temperature of both surfaces thereof is 20° C. or more to a temperature lower than the melting point temperature of the polyolefin-based resin constituting the foam base material. By extending the foam base material, the bubble of the foam base material can be extended and deformed in a predetermined direction, and the aspect ratio of the bubble can be made into a polyolefin-based foam within a predetermined range.

In addition, the extending direction of the foam base material extends in the flow direction or the width direction of the elongated foamable polyolefin resin sheet or in the flow direction and the width direction. Further, when the foam base material is extended in the flow direction and the width direction, the foam base material may be simultaneously extended in the flow direction and the width direction, or may be extended in a single direction.

The method of extending the foam base material in the flow direction, for example, by winding the foam base material in a flow direction to cool the elongated foam sheet while foaming, and winding it at a faster speed (winding speed) The method of extending the speed (supply speed) of the foaming polyolefin resin sheet to the foaming step, and the speed at which the foam substrate is wound to wind the foam substrate (volume) The winding speed is faster than the method of stretching the speed at which the foam substrate is supplied to the stretching step (supply speed).

In addition, in the former method, the foamable polyolefin-based resin sheet expands toward the flow direction due to the foaming of the foamed polyolefin-based resin sheet. Therefore, in the case where the foam base material extends in the flow direction, it is necessary to consider the expandable polyolefin-based resin sheet. After the expansion to the component of the expansion due to the foaming, the supply speed and the winding speed of the foam substrate are adjusted so that the amount of the foam substrate extending toward the flow direction is equal to or greater than the expansion amount.

Further, as a method of extending the foam base material in the width direction, it is preferable that both end portions in the width direction of the foam base material are held by a pair of grip members, and the pair of grip members are placed on each other. The method of slowly moving in the direction of separation to extend the foam substrate in the width direction is preferred. In addition, the foamable polyolefin-based resin sheet expands in the width direction by the foaming of the foamed polyolefin-based resin sheet. Therefore, when the foam base material is extended in the width direction, it is necessary to consider that the foamable polyolefin-based resin sheet is foamed. After expanding the component in the width direction, the foam substrate is adjusted to extend in the width direction so that the amount of elongation becomes more than the expansion component.

Here, the stretching ratio of the polyolefin-based foam is such that the stretching ratio in the flow direction is too small, and the flexibility and tensile strength of the polyolefin-based resin foam substrate are too small. There may be a case of a decrease. If it is too large, there may be a breakage of the foam substrate during the stretching or a foaming gas is detached from the foamed substrate in the foaming, resulting in foaming of the obtained polyolefin resin. The foaming ratio of the bulk substrate is remarkably lowered, and the flexibility and tensile strength of the polyolefin-based resin foam substrate are lowered, and the quality is not uniform, and 1.1 to 2.0 times is preferable, and 1.2 to 1.5 times is more preferable.

Further, if the stretching ratio in the width direction is too small, the flexibility and tensile strength of the polyolefin-based foam substrate may decrease. If the stretching ratio is too large, the foam substrate may be cut during stretching or The foaming gas is detached from the foamed base material during foaming, and the foaming ratio of the obtained polyolefin-based resin foam base material is remarkably lowered, and the flexibility and tensile strength of the polyolefin-based resin foam base material are lowered. In the case of falling and uneven quality, 1.2 to 4.5 times is ideal, and 1.5 to 3.5 times is more desirable.

Further, in the case of extending in the width direction and then extending in the flow direction, the stretching ratio in the width direction should be the same as the stretching ratio in the flow direction, and the stretching ratio in the constant flow direction is preferably the same as the stretching ratio in the width direction.

In order to make the adhesive tape exhibit design, light blocking or concealing properties, light reflectivity, and light resistance, the foam substrate can also be colored. The colorants may be used singly or in combination of two or more.

In the case where the adhesive tape is provided with light-shielding property, concealing property, and light resistance, the foam base material is colored black. Black colorant, carbon black, graphite, copper oxide, manganese dioxide, aniline black, black, titanium black, cyanine black, activated carbon, ferrite, magnetite, chromium oxide, iron oxide , molybdenum disulfide, chromium complex, composite oxide black pigment, lanthanide organic black pigment, and the like. Among them, carbon black is preferred from the viewpoints of cost, availability, insulation, resistance to extrusion of the foamable polyolefin-based resin composition, or heat resistance at the temperature of the heat-expansion step.

In the case where the adhesive tape imparts designability, light reflectivity, etc., the foam base is colored white. White coloring agent, which can use titanium oxide, zinc oxide, aluminum oxide, cerium oxide, magnesium oxide, zirconium oxide, calcium oxide, tin oxide, antimony oxide, antimony oxide, antimony oxide, magnesium carbonate, calcium carbonate, barium carbonate, zinc carbonate , aluminum hydroxide, magnesium hydroxide, calcium hydroxide, zinc hydroxide, aluminum citrate, calcium citrate, barium sulfate, calcium sulfate, barium stearate, zinc oxide, talc, ceria, alumina, clay, Inorganic white colorant such as kaolin, titanium phosphate, mica, gypsum, white carbon, diatomaceous earth, bentonite, lithopone, zeolite, sericite, fluorenone resin particles, acrylic resin particles, uric acid An organic white coloring agent such as an ester resin particle or a melamine resin particle. From the viewpoints of cost, availability, color tone, resistance to extrusion of the foamable polyolefin-based resin composition, or heat resistance at the temperature of the heat-expansion step, alumina or zinc oxide is preferred.

In addition, in the foamable polyolefin resin composition, the plasticizer, the antioxidant, the zinc oxide, etc. may be optionally contained in the resin in the range of the physical properties of the polyolefin-based resin foam substrate. Foaming aids, bubble core adjustment materials, thermal stabilizers, flame retardants such as aluminum hydroxide or magnesium hydroxide, antistatic agents, air balls made of glass or plastic. A known product such as a filler such as a bead, a metal powder or a metal compound, a conductive filler, or a thermally conductive filler. The polyolefin-based resin foam base material used in the adhesive tape of the present invention is preferably from 0.1 to 10% by mass, and preferably from 1 to 7% by mass, based on the polyolefin-based resin, in order to maintain moderate followability and cushioning properties.

Further, the coloring agent, the thermally decomposable foaming agent, the foaming aid, and the like are blended in the foamable polyolefin In the case of the resin composition, from the viewpoint of preventing color unevenness, abnormal foaming, and poor foaming, it is preferable to use a foamable polyolefin resin composition or a foamable polyolefin system before the supply to the extruder. It is preferred that the thermoplastic resin having a high mutual solubility of the resin composition is subjected to a master batch.

The foam substrate may be subjected to corona treatment, flame treatment, plasma treatment, hot air treatment, ozone in order to improve adhesion to the adhesive layer or other layers. Surface treatment such as ultraviolet treatment, application of an easy-to-adhere treatment agent. The surface treatment can be carried out by using a wetting agent to have a wetting index of 36 mN/m or more, preferably 40 mN/m, more preferably 48 mN/m, to obtain good adhesion to the adhesive. The foam base material having improved adhesion can be bonded to the adhesive layer by a continuous step, or can be wound first. When the foam substrate is first wound, in order to prevent the adhesion of the foam substrates which have improved adhesion, it is preferred to use the foam substrate with paper or polyethylene or polypropylene or polyester. It is preferred that the film such as a film is wound together, preferably a polypropylene film or a polyester film having a thickness of 25 μm or less.

[Adhesive layer]

The adhesive layer used in the adhesive tape of the present invention has a thickness of 40 μm or less, preferably 10 to 40 μm. When the thickness of the adhesive layer is within this range, when the organic EL display is reworked, the organic EL display is less likely to be subjected to local stress, and the organic EL display is less likely to be broken, broken, or deformed, and an ideal reworkability can be achieved.

Further, the adhesive force of the adhesive layer is formed by applying a 2 kg roller to the SUS plate under the environment of a temperature of 23 ° C and a relative humidity of 50% RH on a PET substrate having a thickness of 25 μm and a thickness of 25 μm. The peeling speed of the peeling speed of 300 mm/min and the peeling force of the peeling speed of 300 mm/min after the temperature is maintained at a temperature of 23 ° C and a relative humidity of 50% RH for one hour is 0.6 to 2 N / 20 mm, preferably 0.8. ~1.8N/20mm. When the adhesive force is in this range, cracking, breakage, and deformation of the organic EL display are less likely to occur during rework, and ideal impact resistance can be achieved.

The adhesive layer used in the adhesive tape of the present invention preferably exhibits a peak value of the loss tangent (tan δ) at a frequency of 1 Hz, preferably a temperature of -50 ° C to 15 ° C. When the peak value of the loss tangent of the adhesive layer is in this range, it is easy to impart good adhesion to the adherend at normal temperature. especially, When the drop impact resistance is improved in a low temperature environment, -45 ° C ~ 10 ° C is better, and -40 ° C ~ 6 ° C is better.

Loss tangent (tan δ) at a frequency of 1 Hz, which can be obtained from the equation of tan δ=G"/G' from the storage elastic coefficient (G') and the loss elastic modulus (G" obtained by dynamic viscoelasticity measurement by temperature dispersion. . In the measurement of the dynamic viscoelasticity, a viscoelasticity tester (manufactured by TA INSTRUMENTS JAPAN, trade name: ARES G2) was used, and an adhesive layer having a thickness of about 2 mm was formed in a parallel disk having a diameter of 8 mm in the measuring portion of the test machine. The storage elastic modulus (G') and the loss elastic modulus (G") at -60 ° C to 150 ° C were measured at a frequency of 1 Hz as a test piece.

In the tensile test of the adhesive layer, the tensile elongation at the time of cutting is not particularly limited, and the tensile elongation in the flow direction is preferably 200 to 600%, more preferably 250 to 550%, and particularly preferably 250 to 400%. . If the tensile elongation of the adhesive layer is in this range, it is easy to achieve desired reworkability.

Further, in the tensile test of the adhesive layer, the tensile elongation at the time of cutting was performed by using a TENSILON tensile tester at 23 ° C using a sample having a length of 2 cm and a width of 1 cm. In the environment of 50% RH, the elongation at the time of stretching and cutting was performed under the measurement conditions of a tensile speed of 300 mm/min.

As the adhesive composition constituting the adhesive layer of the adhesive tape of the present invention, an adhesive composition which is usually used for an adhesive tape can be used. The adhesive composition is, for example, a (meth)acrylic adhesive, an urethane-based adhesive, a synthetic rubber-based adhesive, a natural rubber-based adhesive, an anthrone-based adhesive, etc., but it is preferable to use An acrylic copolymer composed of a acrylate alone or a copolymer of a (meth) acrylate and another monomer as a base polymer, and if necessary, an additive such as an adhesive-imparting resin or a crosslinking agent is blended as needed. The (meth)acrylic adhesive composition is preferred.

As the acrylic copolymer, an acrylic copolymer mainly containing a (meth) acrylate monomer having 1 to 12 carbon atoms as a monomer component, and a (meth) acrylate having 1 to 12 carbon atoms are preferably used. Methyl acrylate, ethyl (meth) acrylate, n-butyl (meth) acrylate, isobutyl (meth) acrylate, tert-butyl (meth) acrylate, n-hexyl (meth) acrylate, N-octyl (meth)acrylate, isooctyl (meth)acrylate, isodecyl (meth)acrylate, cyclohexyl (meth)acrylate, (meth) propylene One or two or more of these may be used as the monomer such as 2-ethylhexyl acid. Among them, a (meth) acrylate having an alkyl group having a carbon number of 4 to 12 is preferred, and a linear or branched (meth) acrylate having a carbon number of 4 to 9 is more preferable. Among them, a straight chain having a carbon number of 4 to 9 or an acrylate having a branched structure is more preferable.

The content of the (meth) acrylate having 1 to 12 carbon atoms in the acrylic copolymer is preferably 80 to 98.5 mass%, more preferably 90 to 98. mass%, of the monomer components constituting the acrylic copolymer.

Further, the acrylic copolymer used in the present invention may be a copolymer of a highly polar vinyl monomer, and examples of the highly polar vinyl monomer include a vinyl monomer having a hydroxyl group, a vinyl monomer having a carboxyl group, and a fluorene. One or two or more of these may be used.

As the monomer having a hydroxyl group, for example, 2-hydroxyethyl (meth)acrylate, 2-hydroxypropyl (meth)acrylate, 4-hydroxybutyl (meth)acrylate, or (meth)acrylic acid 6 can be used. -Hydroxyhexyl ester or the like having a hydroxyl group-containing (meth) acrylate.

As the vinyl monomer having a carboxyl group, for example, acrylic acid, methacrylic acid, itaconic acid, maleic acid, (meth)acrylic acid dimer, crotonic acid, ethylene oxide-modified succinic acid acrylate, or the like can be used. Among them, acrylic acid is preferred as the copolymerization component.

Further, examples of the monomer having a guanamine group include N-vinylpyrrolidone, N-vinylcaprolactam, and acrylonitrile. Porphyrin, acrylamide, N,N-dimethylpropenamide, and the like.

Examples of the other high-polarity vinyl monomer include a sulfonic acid group-containing monomer such as vinyl acetate, ethylene oxide-modified succinic acid acrylate, and 2-propenylamine-2-methylpropane sulfonic acid. A terminal alkoxy-modified (meth) acrylate such as 2-methoxyethyl acrylate or 2-phenoxyethyl (meth) acrylate.

The content of the highly polar vinyl monomer is preferably from 0.2 to 15% by mass, more preferably from 0.4 to 10% by mass, even more preferably from 0.5 to 6% by mass, based on the monomer component constituting the acrylic copolymer. By including the range, it is easy to adjust the cohesive force, the holding power, and the adhesiveness of the adhesive to a desired range.

Further, in the case where an isocyanate crosslinking agent is used as the crosslinking agent, the vinyl monomer having a functional group reactive therewith is preferably a hydroxyl group-containing vinyl monomer, more preferably 2-hydroxyethyl (meth)acrylate, 4-hydroxybutyl (meth)acrylate or 6-hydroxyhexyl (meth)acrylate. The content of the hydroxyl group-containing vinyl monomer to be reacted with the isocyanate crosslinking agent is preferably 0.1 to 5.0% by mass, more preferably 0.1 to 2.5% by mass, more preferably 0.5 to 1.5, of the monomer component constituting the acrylic copolymer. The quality % is especially good.

The acrylic copolymer can be obtained by copolymerization by a known polymerization method such as a solution polymerization method, a bulk polymerization method, a suspension polymerization method, or an emulsion polymerization method, but from the viewpoint of water resistance of the adhesive, a solution polymerization method or a block form A polymerization method is preferred. In the method of starting the polymerization, a method of using a benzoic acid such as benzoyl peroxide or a oxidized lauric acid such as oxidized lauric acid or an azo-based thermal polymerization initiator such as azobisisobutyl nitrene to start the reaction by heat can be used arbitrarily. Method for starting reaction by ultraviolet irradiation of acetophenone-based, benzoin ether-based, benzyl ketal-based, fluorenylphosphine oxide-based, benzoin-based, and diphenyl ketone-based photopolymerization initiators, and using electrons The method of beam irradiation.

The molecular weight of the above acrylic copolymer is from 40 to 3,000,000, preferably from 800 to 2.5 million, in terms of standard polystyrene, as measured by gel permeation chromatography (GPC).

Here, the measurement of the molecular weight by the GPC method is a standard polystyrene conversion value measured by a GPC apparatus (HLC-8329GPC) manufactured by Tosoh Corporation, and the measurement conditions are as follows.

Sample concentration: 0.5% by mass (THF solution)

Sample injection amount: 100μl

Dissolution: THF

Flow rate: 1.0ml/min

Measuring temperature: 40 ° C

This column: TSKgel GMHHR-H (20) 2

Protection column: TSKgel HXL-H

Detector: Differential Refractometer

Standard polystyrene molecular weight: 10,000 to 20 million (made by Tosoh Co., Ltd.)

In the acrylic pressure-sensitive adhesive composition used in the present invention, an adhesion-imparting resin may be used in order to improve the adhesion to the adherend or the adhesion. Examples of the adhesion-imparting resin include rosin-based, polymerized rosin-based, polymerized rosin-ester-based, rosin-phenol-based, stabilized rosin-ester-based, heterogeneous rosin-ester-based, hydrogenated-rosin-ester-based, terpene-based, and terpene-phenol-based resins. Petroleum resin, (meth) acrylate resin, and the like. When it is used in an emulsion type adhesive composition, it is preferred to use an emulsion type adhesion-imparting resin.

In the acrylic adhesive composition, in order to improve the cohesive force of the adhesive layer, it is preferred to crosslink the adhesive. Examples of such a crosslinking agent include an isocyanate crosslinking agent, an epoxy crosslinking agent, a metal chelate crosslinking agent, and an aziridine crosslinking agent. Among them, a crosslinking agent of a type which is added after the completion of the polymerization and which allows the crosslinking reaction to proceed is preferably an isocyanate crosslinking agent which is rich in reactivity with the (meth)acrylic copolymer and an epoxy crosslinking. The isocyanate crosslinking agent is more preferable from the viewpoint of improving the adhesion to the foam substrate.

Examples of the isocyanate crosslinking agent include methylphenyl diisocyanate, anthranyl-1,5-diisocyanate, hexamethylene diisocyanate, diphenylmethane diisocyanate, xylene diisocyanate, and trishydroxyl. Propane modified methyl phenyl diisocyanate and the like. Particularly preferred is a trifunctional polyisocyanate compound. Examples of the trifunctional isocyanate compound include methylphenyl diisocyanate, such trimethylolpropane adducts, and triphenylmethane isocyanate.

As an index of the degree of crosslinking, the gel fraction of the insoluble component after the adhesive layer is immersed in toluene for 24 hours is 70 to 95% by mass, and more preferably 80 to 93% by mass. If it is in the range of 85 to 93% by mass, the cohesiveness and the adhesion are good.

Further, the gel fraction was measured as follows. The adhesive composition was applied onto the release sheet so that the thickness after drying became 50 μm, dried at 100 ° C for 3 minutes, and aged at 40 ° C for 2 days, and then cut into 50 mm squares to prepare a sample. Then, the weight (G1) of the sample before being immersed in toluene was measured, and the toluene insoluble component of the sample was immersed in a toluene solution at 23 ° C for 24 hours, and then filtered by a 300 mesh metal mesh to separate, and dried at 110 ° C. The residue weight (G2) after 1 hour was determined by the following formula.

Gel fraction (% by mass) = (G2/G1) × 100

As an additive to the adhesive, plasticizer, softener, antioxidant, flame retardant, glass or plastic fiber can be added as needed. Balloon. Fillers, pigments such as beads, metal powders, metal oxides, metal nitrides. A known product such as a coloring agent such as a dye, a coating agent, a tackifier, a water repellent, and an antifoaming agent is used in the adhesive composition.

The adhesive tape of the present invention is an adhesive tape having the above adhesive layer on at least one side, and the adhesive tape of the present invention is made into a double-sided adhesive tape described later, and one of the adhesive layers is the adhesive layer of the above-mentioned weak adhesive force. When the other side is used as an adhesive layer having a strong adhesion to the adhesive layer of the weak adhesive force, the following adhesive layer is preferably used as the adhesive layer of the strong adhesive force.

The thickness of the adhesive layer of the strong adhesive force is preferably the same as the adhesive layer of the weak adhesive force from the viewpoint of easily securing the desired reworkability, preferably 40 μm or less, more preferably 10 to 40 μm.

Further, it is preferable that the adhesion of the adhesive layer of the strong adhesive force is set to an adhesive layer of a thickness of 25 μm on a PET substrate having a thickness of 25 μm, and the adhesive tape is formed in an environment of a temperature of 23 ° C and a relative humidity of 50% RH for SUS. The plate is pressure-bonded by using a 2kg roller in a number of times of crimping, and is allowed to stand for 1 hour in an environment of a temperature of 23 ° C and a relative humidity of 50% RH. The peeling speed of the peeling speed of 300 mm/min is 180 degrees. The adhesive layer of ~25N/20mm is better, and 1.5~20N/20mm is better. Moreover, the 180 degree peeling adhesive force of the adhesive layer of the strong adhesive force is greater than the 180 degree peeling adhesive force of the adhesive layer of the weak adhesive force by 1 N/20 mm or more, preferably 5 to 20 N/20 mm, and more preferably Good for 8~15N/20mm adhesion, easier to selectively strip, ideal.

The adhesive layer of the strong adhesive force preferably exhibits a peak value of the loss tangent (tan δ) at a frequency of 1 Hz, preferably a temperature of -40 ° C to 15 ° C. When the peak value of the loss tangent of the adhesive layer is in this range, it is easy to impart good adhesion to the adherend at normal temperature. In particular, when the drop impact resistance is improved in a low temperature environment, -35 ° C to 10 ° C is more preferable, and -30 ° C to 6 ° C is more preferable.

The adhesive composition constituting the adhesive layer of the strong adhesive force, if it is the range of the above adhesive force, The adhesive layer of the above-mentioned weak adhesion which is used in the usual adhesive tape can be used as the same adhesive composition, and a (meth)acrylic adhesive composition is preferable.

As the acrylic copolymer, an acrylic copolymer mainly containing a (meth) acrylate monomer having 1 to 12 carbon atoms as a monomer component is preferably used as the (meth) acrylate having 1 to 12 carbon atoms. The adhesive layer having the above-mentioned weak adhesion is the same one or two or more kinds of monomers. Among them, a (meth) acrylate having an alkyl group having 4 to 12 carbon atoms is preferred, and a linear or branched (meth) acrylate having a carbon number of 4 to 8 is more preferable. In particular, n-butyl acrylate is preferred because it is easy to ensure adhesion to the adherend, and is excellent in cohesive force or resistance to sebum.

The content of the (meth) acrylate having 1 to 12 carbon atoms in the acrylic copolymer is preferably 80 to 98.5 mass%, more preferably 90 to 98. mass%, of the monomer components constituting the acrylic copolymer.

Further, the acrylic copolymer used in the adhesive layer of the strong adhesive layer may also copolymerize a highly polar vinyl monomer. As the highly polar vinyl monomer, a vinyl monomer having a hydroxyl group and a carboxyl group may be mentioned. One or two or more of these may be used as the vinyl monomer, the vinyl monomer having a mercapto group. As the above-mentioned highly polar vinyl monomer, a monomer which is the same as the above-mentioned weak adhesion adhesive layer can be used, and a vinyl monomer having a carboxyl group, particularly acrylic acid, is preferably used.

The content of the highly polar vinyl monomer is preferably from 1.5 to 20% by mass, more preferably from 1.5 to 10% by mass, even more preferably from 2 to 8% by mass, based on the monomer component constituting the acrylic copolymer. When the content is in this range, it is easy to adjust the cohesive force, the holding power, and the adhesiveness of the adhesive to a desired range.

Further, in the case where an isocyanate crosslinking agent is used as the crosslinking agent, the vinyl monomer having a functional group reactive therewith is preferably a hydroxyl group-containing vinyl monomer, 2-hydroxyethyl (meth)acrylate, ( 4-Hydroxymethyl methacrylate and 6-hydroxyhexyl (meth) acrylate are particularly preferred. The content of the hydroxyl group-containing vinyl monomer to be reacted with the isocyanate crosslinking agent is preferably 0.01 to 1.0% by mass, more preferably 0.03 to 0.3% by mass, based on the monomer component constituting the acrylic copolymer.

The molecular weight of the above acrylic copolymer, the standard polystyrene determined by gel permeation chromatography (GPC) The weight average molecular weight in terms of ethylene is from 4 to 3,000,000, preferably from 80 to 2.5 million. The measurement of the molecular weight by the GPC method was carried out in the same manner as the above-mentioned weak adhesion adhesive layer.

In the acrylic adhesive composition used for the adhesive layer of the strong adhesive force, in order to improve the adhesion to the adherend or the surface adhesive strength, it is preferred to use an adhesive-imparting resin. Examples of the adhesive-imparting resin include rosin-based, polymerized rosin-based, polymerized rosin-ester-based, rosin-phenol-based, stabilized rosin-ester-based, heterogeneous rosin-ester-based, hydrogenated-rosin-ester-based, terpene-based, terpene-phenol-based, and petroleum-based resins. Resin type, (meth) acrylate type resin, etc. When it is used in an emulsion type adhesive composition, it is preferred to use an emulsion type adhesion-imparting resin.

Among them, a heterogeneous rosin ester-based adhesion-imparting resin, a polymerized rosin-based adhesion-imparting resin, a rosin-phenol-based adhesion-imparting resin, a hydrogenated rosin-based adhesion-imparting resin, and a (meth)acrylate-based resin are preferable. One type or two or more types can be used for the adhesion-imparting resin.

The softening point of the adhesive imparting resin is not particularly specified, and is 30 to 180 ° C, preferably 70 ° C to 140 ° C. High adhesion performance can be expected by imparting a resin with a high softening point. In the case of a (meth) acrylate-based adhesion-imparting resin, the glass transition temperature is 30 to 200 ° C, preferably 50 ° C to 160 ° C.

The blending ratio of the acrylic copolymer and the tackifying resin is preferably from 5 to 60 parts by mass, more preferably from 8 to 50 parts by mass, per 100 parts by mass of the acrylic copolymer. By setting the ratio of the two to this range, it is easy to ensure adhesion to the adherend.

In the acrylic adhesive composition, in order to improve the cohesive force of the adhesive layer, it is preferred to crosslink the adhesive. As such a crosslinking agent, it is preferred to use the same crosslinking agent as the above-mentioned weak adhesion adhesive layer, and it is preferred that the crosslinking agent is added after the completion of the polymerization and the crosslinking reaction proceeds, preferably rich. The isocyanate crosslinking agent and the epoxy crosslinking agent which are reactive with the (meth)acrylic copolymer are more preferable from the viewpoint of improving the adhesion to the foam substrate. The isocyanate crosslinking agent is the same crosslinking agent as the above-mentioned weak adhesion adhesive layer.

As an index of the degree of crosslinking, the value of the gel fraction of the insoluble component after the adhesive layer was immersed in toluene for 24 hours was measured. The gel fraction is preferably from 25 to 70% by mass. More preferably, it is 30 to 60% by mass, and more preferably 30 to 55% by mass, and the cohesiveness and adhesion are good.

Moreover, as with the adhesive layer of weak adhesion, a plasticizer, a softener, an antioxidant, a flame retardant, a glass or a plastic fiber as an additive may be optionally added to the adhesive composition. Balloon. Fillers, pigments such as beads, metal powders, metal oxides, metal nitrides. A known product such as a coloring agent such as a dye, a coating agent, a tackifier, a water repellent, and an antifoaming agent.

[adhesive tape]

The adhesive tape of the present invention has the above-mentioned adhesive layer on at least one side of the above-mentioned foam substrate, has excellent impact resistance, and has good workability of the rigid member, and can securely fix the member well. Since the holding force is sheared, even when the flat organic EL display is fixed to the rigid member in the form of a plate, it is possible to suppress the organic EL display from falling off when a force in the shearing direction is applied to the organic EL display. Therefore, the adhesive tape of the present invention can be suitably used for fixing a protective panel of an image display portion of a mobile electronic device such as a smart phone or a tablet type personal computer, or a liquid crystal display module having a glass in a surface layer portion, and an organic EL module. Such as image display module. Moreover, since the rigid body members are excellent in adhesion to each other, the frame or the image display module which is suitable for bonding the protective panel to the image display module or the fixing portion to the flat plate is fixed to the support.

As an embodiment of the adhesive tape of the present invention, the foam base material is basically constituted by a core material, and at least one surface of the base material is preferably provided with an adhesive layer on both surfaces. The substrate and the adhesive layer may be laminated directly or may have other layers. Such an aspect can be appropriately selected depending on the intended use, and when it is desired to further impart dimensional stability or tensile strength to the tape, a laminate layer such as a polyester film may be provided, and when light shielding properties are to be imparted to the tape, light shielding may be imparted. The layer, when ensuring the light reflectivity, can also be provided with a reflective layer. When these other layers are provided, a waterproof layer is used as the other layer.

When two or more members are fixed, in the form of a single-sided adhesive tape, one of the fixed members may be attached to other members via another adhesive tape or adhesive, and if it is a double-sided adhesive tape Form, easy to fix between components, ideal. In the case of a double-sided adhesive tape, the adhesive layer on both sides can be used as the adhesive layer of the weak adhesion of the 180-degree peeling adhesive force of 0.6 to 2 N/20 mm, or the adhesive layer of the weak adhesive force on one side. Further, the other surface is an adhesive layer having a strong adhesion to the adhesive layer of the weak adhesive force, whereby it is preferable to peel off from the desired member side at the time of peeling.

As the laminate layer, a polyester film such as polyethylene terephthalate or a film made of various resins such as a polyethylene film or a polypropylene film can be used. The thickness of the film is preferably from 1 to 16 μm, more preferably from 2 to 12 μm, in terms of followability of the foam substrate.

As the light-shielding layer, a layer formed of a black ink containing a coloring agent such as a pigment can be easily used, and a layer composed of a black ink is preferable because it is excellent in light-shielding property. The reflective layer can be easily used as a layer formed of a white ink. The thickness of these layers is preferably 2 to 20 μm, and 4 to 6 μm is more desirable. When the thickness is within this range, curling of the substrate due to hardening shrinkage of the ink is less likely to occur, and the workability of the tape is good.

The adhesive tape of the present invention can be produced by a conventionally known method. For example, after applying the adhesive composition directly to the surface of the foam substrate or on the surface of another layer laminated on the foam substrate, the direct printing method is dried, or the adhesive is coated on the release sheet. After the material is dried, it is applied to a transfer method of a foam substrate or other layer surface. Further, the adhesive layer is obtained by drying a composition in which an acrylic adhesive composition and a crosslinking agent are blended, and if the adhesive tape is prepared, it is at 20 ° C to 50 ° C, preferably 23 ° C to 45 ° C. In the environment of 2 to 7 days, the adhesion between the foam base material and the adhesive layer or the adhesive property is stabilized, which is preferable.

The thickness of the adhesive tape of the present invention can be appropriately adjusted according to the state of use, but it is preferably used as a small and thin type of mobile electronic device, preferably 500 μm or less, more preferably 100 to 400 μm, and more preferably 120 μm to 350 μm. 130~250μm is especially good. By making the tape thickness the thickness, for the thin type. Small mobile electronic devices are also ideally used, and can achieve excellent reworkability with good followability or impact resistance.

The adhesive tape of the present invention is pressed against the glass plate by a 2kg roller at a temperature of 23 ° C and a relative humidity of 50% RH, and is pressed back and forth once in a pressure of 23 ° C and a relative humidity of 50% RH. After 1 hour, the peeling speed of 300 mm/min is 180 degrees. The peeling adhesive force is preferably 0.2 to 6 N/20 mm, more preferably 0.5 to 5 N/20 mm. Moreover, when the adhesive tape layer having a weak adhesive force and the adhesive layer of the adhesive layer having a strong adhesive force are formed, the adhesive force when the adhesive layer of the weak adhesive force is adhered to the glass plate is preferably the above range. Preferably.

The release sheet used in the present invention is not particularly limited, and examples thereof include at least a synthetic resin film such as polyethylene, polypropylene or polyester film, paper, non-woven fabric, cloth, foamed sheet or metal foil, and substrates such as these laminates. A peeling treatment such as an anthrone-based treatment, a long-chain alkyl group treatment, or a fluorine-based treatment for improving the peeling property from the adhesive is performed on one side.

Among them, a high-quality paper obtained by laminating polyethylene having a thickness of 10 to 40 μm on both sides or a release sheet having an oxime-based release treatment on one side or both sides of a substrate of the polyester film is preferable.

Since the adhesive tape of the present invention has excellent adhesiveness, impact resistance, and reworkability, it can be desirably fixed to an organic EL display which is thin and easily broken or deformed, and can be expensive organic EL when reworked. The display is peeled off without damage or deformation. In particular, when the organic EL display is fixed to a support member such as a support for a mobile electronic device or a plate-shaped rigid member such as a frame, for example, when it is fixed to a plate-shaped rigid member such as a metal support such as SUS or a plate-shaped plastic frame, it is particularly difficult to peel off. The adhesive tape of the present invention can ideally fix the organic EL display even in the fixing step, and the organic EL display is not easily peeled off even when the force is applied in the shearing direction, and good good workability can be achieved. Among them, the fixing of an organic EL display using a glass panel of 0.6 mm or less, preferably 0.5 mm or less in the surface layer can be preferably used.

The adhesive tape of the present invention has such excellent characteristics, and therefore, an organic EL display can be preferably used as an electronic notepad for a video display device, a mobile phone, a PHS, a digital camera, a music player, a television, a notebook personal computer, a smart phone. Mobile electronic devices such as tablet PCs and game consoles, or electronic devices such as wall-mounted TVs, screens, and personal computers.

(Preparation of adhesive solution (1))

In a reaction vessel equipped with a stirrer, a reflux condenser, a thermometer, a dropping funnel, and a nitrogen inlet, 88.6 parts by mass of 2-ethylhexyl acrylate, 10 parts by mass of methyl acrylate, 1 part by mass of acrylic acid, and 4-hydroxy acrylate. 0.4 parts by mass of butyl ester, 0.1 parts by mass of 2,2'-azobisisobutyronitrile as a polymerization initiator, dissolved in a solvent consisting of 150 parts by mass of ethyl acetate, and polymerized at 70 ° C for 12 hours to obtain a weight. An acrylic copolymer (1) having an average molecular weight of 1.97 million (in terms of polystyrene). Then, ethyl acetate was added and uniformly mixed to obtain a 30% non-volatile component of the adhesive solution (1).

(Preparation of adhesive solution (2))

In a reaction vessel equipped with a stirrer, a reflux condenser, a thermometer, a dropping funnel, and a nitrogen inlet, 83.6 parts by mass of 2-ethylhexyl acrylate, 15 parts by mass of methyl acrylate, 1 part by mass of acrylic acid, and 4-hydroxy acrylate. 0.4 parts by mass of butyl ester and 0.1 parts by mass of 2,2'-azobisisobutyronitrile as a polymerization initiator were dissolved in a solvent consisting of 150 parts by mass of ethyl acetate, and polymerization was carried out at 70 ° C for 12 hours to obtain a weight average. An acrylic copolymer (1) having a molecular weight of 1.7 million (in terms of polystyrene). Then, ethyl acetate was added and uniformly mixed to obtain a 30% non-volatile component of the adhesive solution (2).

(Preparation of adhesive solution (3))

73 parts by mass of 2-ethylhexyl acrylate, 25 parts by mass of methyl acrylate, 1 part by mass of acrylic acid, and 2-hydroxy acrylate in a reaction vessel equipped with a stirrer, a reflux condenser, a thermometer, a dropping funnel, and a nitrogen inlet. 1 part by mass of ethyl ester and 0.1 part by mass of 2,2'-azobisisobutyronitrile as a polymerization initiator, dissolved in a solvent consisting of 150 parts by mass of ethyl acetate, and polymerized at 70 ° C for 12 hours to obtain a weight. An acrylic copolymer (3) having an average molecular weight of 1.38 million (in terms of polystyrene). Then, ethyl acetate was added and uniformly mixed to obtain a 30% non-volatile component of the adhesive solution (3).

(Preparation of adhesive solution (4))

With a mixer, reflux cooler, thermometer, dropping funnel and nitrogen inlet In the container, 93.4 parts by mass of n-butyl acrylate, 3.5 parts by mass of acrylic acid, 3 parts by mass of ethyl acetate, 0.1 parts by mass of 2-hydroxyethyl acrylate, and 2, 2'-azo double as a polymerization initiator. 0.1 parts by mass of isobutyronitrile was dissolved in a solvent consisting of 100 parts by mass of ethyl acetate, and polymerization was carried out at 70 ° C for 12 hours to obtain an acrylic copolymer (4) having a weight average molecular weight of 1.6 million (in terms of polystyrene). Then, 9.4 parts by mass of "SUPERESTER A100" (glycerol ester of uneven rosin) manufactured by Arakawa Chemical Co., Ltd., and "HARITAC PCJ" manufactured by Soy Chemicals Co., Ltd. (polymerized rosin pentaerythritol) were added to 100 parts by mass of the acrylic copolymer (4). Ester) 9.4 parts by mass, and ethyl acetate was added and uniformly mixed to obtain a 38% non-volatile component of the adhesive solution (4).

(Preparation of adhesive solution (5))

In a reaction vessel equipped with a stirrer, a reflux condenser, a thermometer, a dropping funnel, and a nitrogen inlet, 74.9 parts by mass of n-butyl acrylate, 20 parts by mass of 2-ethylhexyl acrylate, 2.0 parts by mass of acrylic acid, and vinyl acetate. 3 parts by mass, 0.1 parts by mass of 4-hydroxybutyl acrylate, and 0.1 parts by mass of 2,2'-azobisisobutyronitrile as a polymerization initiator, dissolved in a solvent consisting of 100 parts by mass of ethyl acetate, 70 The polymerization was carried out for 12 hours at ° C to obtain an acrylic copolymer (5) having a weight average molecular weight of 1.2 million (in terms of polystyrene). Then, 20 parts by mass of "PENSEL D135" (pentaerythritol ester of polymerized rosin) manufactured by Arakawa Chemical Co., Ltd. was added to 100 parts by mass of the acrylic copolymer (4), and ethyl acetate was added thereto, and the mixture was uniformly mixed to obtain a nonvolatile component of 50%. Adhesive solution (5).

(Preparation of adhesive solution (6))

In a reaction vessel equipped with a stirrer, a reflux condenser, a thermometer, a dropping funnel, and a nitrogen inlet, 97.97 parts by mass of n-butyl acrylate, 2.0 parts by mass of acrylic acid, and 0.03 parts by mass of 4-hydroxybutyl acrylate were used as polymerization initiation. 0.1 parts by mass of 2,2'-azobisisobutyronitrile dissolved in a solvent consisting of 100 parts by mass of ethyl acetate, and polymerized at 70 ° C for 12 hours to obtain a weight average molecular weight of 1.6 million (in terms of polystyrene) Acrylic copolymer (6). Then, 25 parts by mass of "SUPER ESTER A100" (glycerol ester of uneven rosin) manufactured by Arakawa Chemical Co., Ltd., and "PENSEL D135" manufactured by Arakawa Chemical Co., Ltd. (polymerized rosin) were added to 100 parts by mass of the acrylic copolymer (6). 5 parts by mass of pentaerythritol ester), 20 parts by mass of FTR 6100 (styrene-based petroleum resin) manufactured by Mitsui Chemicals Co., Ltd., and added with ethyl acetate, and uniformly mixed to obtain a 40% non-volatile component adhesive solution. (6).

(Preparation of adhesive solution (7))

88 parts by mass of 2-ethylhexyl acrylate, 8 parts by mass of 2-methoxyethyl acrylate, and 1 part by mass of acrylic acid in a reaction vessel equipped with a stirrer, a reflux condenser, a thermometer, a dropping funnel, and a nitrogen inlet. 3 parts by mass of 4-hydroxybutyl acrylate, 2 parts by mass of 2,2'-azobisisobutyronitrile as a polymerization initiator, dissolved in a solvent consisting of 150 parts by mass of ethyl acetate, and carried out at 70 ° C for 12 hours. Polymerization was carried out to obtain an acrylic copolymer (7) having a weight average molecular weight of 2.02 million (in terms of polystyrene). Then, ethyl acetate was added and uniformly mixed to obtain a 30% non-volatile component of the adhesive solution (7).

[Example 1]

(Preparation of double-sided adhesive tape)

To 100 parts by mass of the above-mentioned adhesive solution (1), 0.67 parts by mass of "CORONATE L-45" (isocyanate-based crosslinking agent, solid content: 45%) manufactured by Nippon Polyurethane Co., Ltd. was added and stirred for 15 minutes, and then the coating was peeled off. The peeled-treated surface of the PET film having a thickness of 75 μm was treated to have a thickness of 20 μm and dried at 80 ° C for 3 minutes to form a weak adhesive layer. The gel fraction of the weak adhesive layer was 86% by mass, and the temperature at the peak of the loss tangent (tan δ) at a frequency of 1 Hz was -36 °C.

Then, 1.1 parts by mass of "CORONATE L-45" (isocyanate-based crosslinking agent, solid content: 45%) manufactured by Nippon Polyurethane Co., Ltd. was added to 100 parts by mass of the above-mentioned adhesive solution (4), and the mixture was stirred for 15 minutes, and then applied to the solution. The peeled-treated surface of the PET film having a thickness of 75 μm which was peeled off was dried to a thickness of 25 μm, and dried at 80° C. for 3 minutes to form a strong adhesive layer. The gel fraction of the strong adhesive layer was 48% by mass, and the temperature at the peak value of the loss tangent (tan δ) at a frequency of 1 Hz was -16 °C.

Then, the black polyolefin-based foam (1) (thickness: 100 μm, interlayer strength: 12.6 N/cm, apparent density 0.40 g/cm ³ , 25% compressive strength: 103 kPa, tensile strength in the flow direction: 1084 N/ cm ^2, a tensile strength of width direction: 790N / cm ^2, corona-treated surface side of a substrate so that the wetting index of 52mN / m, Sekisui chemical (shares) Corporation) the configuration, the bonding 1 The weak adhesive layer was bonded to the opposite side with a strong adhesive layer, and then laminated at 23 ° C under the following line pressure of 5 kg/cm. Thereafter, it was aged at 40 ° C for 48 hours to obtain a double-sided adhesive tape having a thickness of 145 μm.

[Embodiment 2]

The adhesive solution (1) was replaced with an adhesive solution (2), and "CORONATE L-45" (isocyanate-based crosslinking agent, solid content 45%) was added to 100 parts by mass of the adhesive solution (2). After 0.89 parts by mass, a double-sided adhesive tape having a thickness of 145 μm was obtained in the same manner as in Example 1 except that the weak adhesive layer was used. The gel fraction of the weak adhesive layer was 90% by mass, and the temperature at the peak value of the loss tangent (tan δ) at a frequency of 1 Hz was -31 °C.

[Example 3]

The adhesive solution (1) was replaced with an adhesive solution (3), and "CORONATE L-45" (isocyanate-based crosslinking agent, solid content 45%) was added to 100 parts by mass of the adhesive solution (3). After 1.80 parts by mass, a double-sided adhesive tape having a thickness of 145 μm was obtained in the same manner as in Example 1 except that the weak adhesive layer was used. The gel fraction of the adhesive layer was 92% by mass, and the temperature at the peak value of the loss tangent (tan δ) at a frequency of 1 Hz was -25 °C.

[Example 4]

The black polyolefin-based foam (1) was replaced with a black polyolefin-based foam (2) (thickness: 200 μm, interlayer strength: 12.9 N/cm, apparent density: 0.20 g/cm ³ , 25% compressive strength: 52 kPa, tensile strength in the flow direction: 495 N/cm ² , tensile modulus in the width direction: 412 N/cm ² , surface was corona treated to make the wetness index 52 mN/m, manufactured by Sekisui Chemical Industry Co., Ltd., except A double-sided adhesive tape having a thickness of 245 μm was obtained in the same manner as in Example 1 except for the above.

[Example 5]

The black polyolefin-based foam (1) was replaced with a black polyolefin-based foam (3) (thickness: 80 μm, interlayer strength: 10.3 N/cm, apparent density: 0.41 g/cm ³ , 25% compressive strength: 92 kPa, tensile strength in the flow direction: 1062 N/cm ² , tensile modulus in the width direction: 962 N/cm ² , and the surface was corona treated to have a wetness index of 52 mN/m, manufactured by Sekisui Chemical Industry Co., Ltd., except A double-sided adhesive tape having a thickness of 125 μm was obtained in the same manner as in Example 1 except for this.

[Embodiment 6]

The black polyolefin-based foam (1) was replaced with a black polyolefin-based foam (4) (thickness: 120 μm, interlayer strength: 16.0 N/cm, apparent density: 0.38 g/cm ³ , 25% compressive strength: 118 kPa, tensile strength in the flow direction: 994 N/cm ² , tensile modulus in the width direction: 713 N/cm ² , surface was corona treated to achieve a wetness index of 52 mN/m, manufactured by Sekisui Chemical Industry Co., Ltd., except A double-sided adhesive tape having a thickness of 165 μm was obtained in the same manner as in Example 1 except for the above.

[Embodiment 7]

A double-sided adhesive tape having a thickness of 135 μm was obtained in the same manner as in Example 1 except that the thickness of the weak adhesive layer was changed from 20 μm to 10 μm.

[Embodiment 8]

A double-sided adhesive tape having a thickness of 165 μm was obtained in the same manner as in Example 3 except that the thickness of the weak adhesive layer was changed to 20 μm to 40 μm.

[Embodiment 9]

The adhesive solution (4) was replaced with an adhesive solution (5), and "CORONATE L-45" (isocyanate-based crosslinking agent, solid content 45%) was added to 100 parts by mass of the adhesive solution (5). After 1.77 parts by mass, a double-sided adhesive tape having a thickness of 145 μm was obtained in the same manner as in Example 1 except that it was used for a strong adhesive layer. The gel fraction of the adhesive layer was 46% by mass, and the temperature at the peak value of the loss tangent (tan δ) at a frequency of 1 Hz was -7 °C.

[Embodiment 10]

The adhesive solution (4) was replaced with an adhesive solution (6), and "CORONATE L-45" (isocyanate-based crosslinking agent, solid content 45%) was added to 100 parts by mass of the adhesive solution (6). After 1.33 parts by mass, a double-sided adhesive tape having a thickness of 145 μm was obtained in the same manner as in Example 1 except that the adhesive layer was used. The gel fraction of the adhesive layer was 37% by mass, and the temperature at the peak value of the loss tangent (tan δ) at a frequency of 1 Hz was 2 °C.

[Comparative Example 1]

The adhesive solution (1) was replaced with an adhesive solution (7), and "CORONATE L-45" (isocyanate-based crosslinking agent, solid content 45%) was added to 100 parts by mass of the adhesive solution (7). A double-sided adhesive tape having a thickness of 145 μm was obtained in the same manner as in Example 1 except that 0.89 parts by mass was used for the weak adhesive layer. The gel fraction of the weak adhesive layer was 87% by mass, and the temperature at the peak value of the loss tangent (tan δ) at a frequency of 1 Hz was -38 °C.

[Comparative Example 2]

A double-sided adhesive tape having a thickness of 145 μm was obtained in the same manner as in Example 1 except that the amount of the crosslinking agent of the weak adhesive layer was changed to 0.64 parts by mass. The gel fraction of the weak adhesive layer was 81% by mass, and the temperature at the peak value of the loss tangent (tan δ) at a frequency of 1 Hz was -37 °C.

[Comparative Example 3]

A double-sided adhesive tape having a thickness of 145 μm was obtained in the same manner as in Example 3 except that the amount of the crosslinking agent of the weak adhesive layer was changed from 1.80 parts by mass to 1.33 parts by mass. The gel fraction of the weak adhesive layer was 87% by mass, and the temperature at the peak value of the loss tangent (tan δ) at a frequency of 1 Hz was -25 °C.

[Comparative Example 4]

The black polyolefin-based foam (1) was replaced with a black polyolefin-based foam (5) (thickness: 300 μm, interlayer strength: 22 N/cm, apparent density: 0.20 g/cm ³ , 25% compressive strength: 90 kPa) The tensile modulus of elasticity in the flow direction is 530 N/cm ² , the tensile modulus of elasticity in the width direction is 340 N/cm ² , the surface is corona treated to make the wetness index 52 mN/m, and the water vapor chemical industry (stock) company makes 52 mN/m. A double-sided adhesive tape having a thickness of 345 μm was obtained in the same manner as in Example 1 except that INOAC CORPORATION (manufactured by INOAC CORPORATION).

[Comparative Example 5]

The black polyolefin-based foam (1) was replaced with a black polyolefin-based foam (6) (thickness: 140 μm, interlayer strength: 19.1 N/cm, apparent density 0.40 g/cm ³ , 25% compressive strength: 130 kPa, tensile strength in the flow direction: 994 N/cm ² , tensile strength in the width direction: 713 N/cm ² , surface wetness measurement to 52 mN/m, 52 mN/m manufactured by Sekisui Chemical Co., Ltd. A double-sided adhesive tape having a thickness of 185 μm was obtained in the same manner as in Example 1 except that INOAC CORPORATION (manufactured by INOAC CORPORATION).

[Comparative Example 6]

The black polyolefin-based foam (1) was replaced with a black polyolefin-based foam (7) (thickness: 100 μm, interlayer strength: 8.9 N/cm, apparent density: 0.33 g/cm ³ , 25% compressive strength: 70 kPa, tensile strength in the flow direction: 799 N/cm ² , tensile strength in the width direction: 627 N/cm ² , surface was corona treated to have a wetness index of 52 mN/m, and 52 mN/m manufactured by Sekisui Chemical Industry Co., Ltd. A double-sided adhesive tape having a thickness of 145 μm was obtained in the same manner as in Example 1 except that INOAC CORPORATION (manufactured by INOAC CORPORATION).

[Comparative Example 7]

A double-sided adhesive tape having a thickness of 175 μm was obtained in the same manner as in Example 2 except that the thickness of the weak adhesive layer after drying was changed to 20 μm.

[Comparative Example 8]

The black polyolefin-based foam (1) was replaced with a film made of polyethylene terephthalate (PET) (thickness: 25 μm, surface was corona treated to have a wetness index of 52 mN/m), and used for double A double-sided adhesive tape having a thickness of 70 μm was obtained in the same manner as in Example 1 except for the substrate of the surface adhesive tape.

[Comparative Example 9]

The black polyolefin-based foam (1) was replaced with a film made of polyethylene terephthalate (PET) (thickness: 50 μm, surface was corona treated to have a wetness index of 52 mN/m), and used for double A double-sided adhesive tape having a thickness of 95 μm was obtained in the same manner as in Example 1 except for the substrate of the surface adhesive tape.

[Comparative Example 10]

Replace the adhesive solution (1) with the adhesive solution (4), and replace the weak adhesive layer with "CORONATE L-45" (isocyanate system) manufactured by Nippon Polyurethane Co., Ltd. with respect to 100 parts by mass of the adhesive solution (4). The cross-linking agent and the solid content of 45%) of 1.1 parts by mass, in addition to the examples, 1 A double-sided adhesive tape having a thickness of 145 μm was obtained in the same manner. The gel fraction of the adhesive layer was 48% by mass, and the temperature at the peak value of the loss tangent (tan δ) at a frequency of 1 Hz was -16 °C.

The foam base material used in the above examples and comparative examples, and the double-sided adhesive tape obtained in the above examples and comparative examples were evaluated as follows. The results obtained are shown in the table.

[Thickness of foam substrate and adhesive tape]

It was measured by the G type of the dial thickness gauge manufactured by Ozaki. In the case of an adhesive tape, the peeling film is peeled off and measured.

[Interlayer strength of foam substrate]

1.3 parts by mass of "CORONATE L-45" (isocyanate-based crosslinking agent, solid content: 45%) manufactured by Nippon Polyurethane Co., Ltd. was added to 100 parts by mass of the adhesive solution (6), and the mixture was stirred for 15 minutes, and then applied to the peeled off. The peeled-treated surface of the PET film having a thickness of 75 μm was treated to have a thickness of 50 μm after drying, and dried at 80 ° C for 3 minutes to form an adhesive layer. Then, one sheet of the above-mentioned adhesive layer was bonded to both sides of the foam for evaluating the interlayer strength, and then laminated at 23 ° C with a roll having a linear pressure of 5 kgf/cm. Thereafter, the mixture was aged at 40 ° C for 48 hours to obtain a double-sided adhesive tape for measuring the interlayer strength.

Then, the one-side adhesive surface was made to have a width of 1 cm by a substrate of a polyethylene terephthalate film having a thickness of 25 μm (the side bonded to the adhesive surface was corona treated to have a wetness index of 52 mN/m). A double-sided adhesive tape sample having a length of 10 cm (flow direction of the foam substrate) was applied to a polyethylene terephthalate having a thickness of 50 μm by applying a back-and-pressure pressure at 23 ° C and 50% RH using a 2 kg roller. The film (the side adhered to the adhesive surface was subjected to corona treatment to have a wetting index of 52 mN/m), and allowed to stand at 60 ° C for 48 hours. After standing at 23 ° C for 24 hours, the polyethylene terephthalate film side having a thickness of 50 μm was fixed to a high-speed peeling tester (TE-703 manufactured by TESTER Industries Co., Ltd.) with a double-sided adhesive tape for fixing. After the test piece mounting table, the polyester film side having a thickness of 25 μm was stretched at a tensile speed of 15 m/min in a direction of 90 degrees at 23 ° C, and the maximum strength when the foam was pulled (substrate destruction) was measured. (Unit: N/cm)

[Tensile Strength]

A foam substrate or a double-sided adhesive tape (peeling film peeled off) of a test piece having a line spacing of 2 cm (flow direction and width direction of the foam substrate) and a width of 1 cm was processed at a tensile speed of 300 mm/min. The stretching was performed, and the strength at the time of cutting was measured. Then, the measured value was divided by the thickness of the foam substrate to calculate the tensile strength. (Unit: N/cm ² )

[Tensile elongation]

The foam substrate or the double-sided adhesive tape (peeling film peeled off) which was processed into a test piece having a line spacing of 2 cm and a width of 1 cm was stretched at a stretching speed of 300 mm/min along the flow direction of the foam substrate. The elongation at the time of cutting was taken as the tensile elongation.

[Average bubble diameter in the flow direction and width direction of the foam substrate]

The foam substrate was cut into 1 cm in the width direction and in the flow direction. Then, the central portion of the cut surface of the cut foam substrate was magnified 200 times by a digital microscope (trade name "KH-7700", manufactured by HiROX Co., Ltd.), and the width direction or flow direction of the foam substrate was taken. The cross section allows the cut surface of the foam substrate to be accommodated in the photograph along the entire length of the substrate. From the photographs obtained, the bubble diameters of the bubbles existing on the cut surface having an actual length of 2 mm before the enlargement in the flow direction or the width direction were measured, and the average bubble diameter was calculated from the average value thereof. The average bubble diameter was measured at any 10 points as the average bubble diameter in the flow direction (MD) and the width direction (CD).

[Average bubble diameter in the thickness direction of the foam substrate]

The average cell diameter in the thickness direction of the foam substrate is observed under a microscope under the same conditions as the average cell diameter of the flow direction of the foam substrate, and the diameter of the bubble in the flow direction or the width direction in the photograph obtained by the measurement is observed. The bubbles were all measured in the thickness direction of the bubble diameter, and the average bubble diameter was calculated from the average value. This was measured at arbitrary 10 points, and the average value was taken as the average bubble diameter in the thickness direction (CD). Further, it is the average bubble diameter in the thickness direction (CD).

[180 degree peel adhesion (adhesive layer)]

The 180-degree peeling adhesion of each of the adhesive layers used in the examples and the comparative examples was measured by the following method.

1) 100 parts by mass of each of the adhesive compositions described in the examples and the comparative examples, In the examples and comparative examples, a crosslinking agent was added, and after stirring for 15 minutes, it was applied onto a PET film having a thickness of 75 μm which was subjected to release treatment, and the thickness after drying was 25 μm, and dried at 80 ° C for 3 minutes to form an adhesive layer. Then, after bonding the above-mentioned adhesive layer to a polyethylene terephthalate film having a thickness of 25 μm (the side bonded to the adhesive surface by a corona treatment to have a wetness index of 52 mN/m), a linear pressure of 5 kgf was applied at 23 ° C. The /cm roller was laminated. Thereafter, the mixture was aged at 40 ° C for 48 hours to prepare an adhesive tape for measuring adhesion.

2) Using a 2kg roller in an environment with a temperature of 23 ° C and a relative humidity of 50% RH, press the stainless steel plate one by one with the number of crimping times (the hairline finish is processed with water resistant paper of SUS304, #360) )).

3) The strength (unit: N/20 mm) when peeled in a direction of 180 degrees at a tensile speed of 300 mm/min at 23 ° C, 50% RH, after standing at 23 ° C, 50% RH for 1 hour.

[180 degree peel adhesion (adhesive tape)]

The 180-degree peel adhesion of the adhesive tapes of the examples and the comparative examples was measured by the following method.

1) The strong adhesive side is made of a polyethylene terephthalate film having a thickness of 25 μm (the side adhered to the adhesive surface is corona treated to have a wetness index of 52 mN/m) and the width is 2 cm. A double-sided adhesive tape sample having a length of 10 cm (flow direction of the foam substrate) is bonded to a stainless steel plate having a thickness of 1.5 mm (SUS304, surface BA) by using a 2 kg roller back and forth at 23 ° C at 50% RH. The processing is the same as the following) or an alkali-free glass ("EAGLE-XG" manufactured by Corning Incorporated) having a thickness of 0.5 mm.

2) The strength (unit: N/20 mm) at the time of stretching at a tensile speed of 300 mm/min in a direction of 180 degrees at 23 ° C, 50% RH, after standing at 23 ° C, 50% RH for 1 hour.

[Impact resistance test]

1) Two sheets of a length of 40 mm and a width of 5 mm are laminated in parallel at intervals of 40 mm in an acrylic plate having a thickness of 2 mm and an outer shape of 50 mm × 50 mm (Mitsubishi Riyang (share) ACRYLITE L "trade name", hue: transparent). After the weak adhesive surface of the double-sided adhesive tape (Fig. 1), it is bonded to an ABS board having a thickness of 2 mm and a shape of 150 mm × 100 mm (made by Sumitomo Bakelite Co., Ltd., TOUGHACE R "trade name" Hue: natural, no embossing, the same below The central part (Figure 2). After pressurizing back and forth once with a 2 kg roller, it was allowed to stand at 23 ° C for 1 hour to obtain a test piece.

2) Set the length on the pedestal of the DuPont impact tester (manufactured by TESTER Industries Co., Ltd.) A 150 mm, a width of 100 mm, and a height of 45 mm was used to measure the test piece (aluminum made of 5 mm thick) on which the test piece was taken up with an acrylic plate (Fig. 3). From the side of the ABS plate, the core made of stainless steel with a diameter of 25 mm and a mass of 300 g was changed by 10 cm each time, and dropped to the center of the ABS plate at intervals of 10 seconds at each height for 5 times. The height at which it has been stripped or destroyed.

◎: After the height of 80cm test, the tape still has no peeling and damage

○: After the test of height 70~80cm, the tape is peeled off or destroyed by the invention.

×: After the test of height 50~60cm, the tape peeled off or destroyed

××: peeling or damage of the tape after the test with a height of 40 cm or less

[heavy workability]

1) The weak adhesive surface of the double-sided adhesive tape having a shape of 30 mm × 30 mm is attached to an alkali-free glass plate having a thickness of 0.5 mm and a shape of 30 mm × 30 mm. Next, a SUS plate (SUS304, surface BA processing) having a thickness of 0.5 mm and an outer shape of 30 mm × 100 mm was attached, and the mixture was pressed once and twice with a 2 kg roller, and then left at 23 ° C for 24 hours to prepare a test piece.

2) Evaluation of the ease of peeling when the alkali-free glass plate was peeled off in the vertical direction at 23 °C.

○: It can be easily peeled off without breaking the alkali-free glass.

×: The alkali-free glass was broken and could not be peeled off.

[Shear retention test]

1) A double-sided adhesive tape sample having a width of 2 cm and a length of 7 cm (flow direction of a foam substrate) obtained by using an aluminum foil substrate having a thickness of 50 μm on the strong adhesive side of the adhesive tape of the examples and the comparative examples, at a temperature 23 ° C, relative humidity 50% RH environment, using a 2kg roller to crimp back and forth to a thickness of 1.5mm, vertical 40mm × horizontal 50mm stainless steel plate (with SUS304, #360 water-resistant paper in the longitudinal direction of the thin line The processing is such that the bonding area becomes 2 cm in length × 2 cm in width. The test piece was prepared by allowing to stand at 23 ° C and 50% RH for 1 hour.

2) After the test piece was allowed to stand in an environment of 90 ° C for 1 hour, the stainless steel plate side of the test piece was attached to a holding force tester (manufactured by TESTER Industries) having a temperature of 90 ° C in the layer, and the end of the double-sided adhesive tape side was used. A load of 500 g was installed in the section, and a load was applied to the shear direction of the adhesive surface of the double-sided adhesive tape and the stainless steel, and the test was started. After 24 hours, it was evaluated whether the double-sided adhesive tape was peeled off from the stainless steel plate. (Figure 4)

○: The double-sided adhesive tape was not peeled off.

×: The double-sided adhesive tape peeled off.

As in the above Examples 1 to 10, the adhesive tape of the present invention has excellent impact resistance and followability with the adherend, and has good reworkability. Further, the adhesive tapes of the present invention of Examples 1 to 10 have a good shear holding force which hardly deviates even if the deviation distance after 24 hours is 1 mm or less. On the other hand, the adhesive tapes of Comparative Examples 1 to 10 did not have ideal impact resistance, followability, and reworkability.

Claims (6)

An adhesive tape which is fixed to an organic EL display and has an adhesive layer on at least one side of the foam substrate, and the thickness of the foam substrate is 250 μm or less and the interlayer strength is 10 to 18 N/cm. The adhesive layer is a thickness of 40 μm or less, and an adhesive tape formed by setting an adhesive layer of a thickness of 25 μm on a PET substrate having a thickness of 25 μm is pressed at a temperature of 23° C. and a relative humidity of 65% RH using a 2 kg roller. The SUS plate was pressure-bonded once and again, and allowed to stand for 1 hour in an environment of a temperature of 23 ° C and a relative humidity of 50% RH, and a peeling force of 0.6 to 2 N / 25 mm at a peeling speed of 300 mm/min. For example, in the adhesive tape of claim 1, the organic EL display is fixed to the plate-shaped rigid body member. The adhesive tape of claim 1 or 2, wherein the foam substrate has a 25% compressive strength of 30 kPa or more. The adhesive tape of claim 1 or 2, wherein the foam substrate has an apparent density of 0.1 to 0.7 g/cm ³ . The adhesive tape of claim 1 or 2, wherein the foam substrate is a polyolefin-based foam substrate. The adhesive tape of claim 1 or 2, wherein the adhesive layer on one side of the foam substrate is provided with a thickness of 25 μm on the PET substrate having a thickness of 25 μm and the adhesive tape is formed at a temperature of 23 ° C. In the case of a relative humidity of 50% RH, the SUS plate is pressed with a 2 kg roller one by one, and the peeling speed is allowed to stand for one hour in an environment of a temperature of 23 ° C and a relative humidity of 50% RH. The 180 degree peel adhesion of 300mm/min is 1~25N/20mm.