JP2017014529A - Adhesive tape, sheet and article for binding harness - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide an adhesive tape capable of holding adhesion over long time without causing detachment on a boundary surface between an adherend and an adhesive layer even when used for adhesion of the adherend containing a plasticizer.SOLUTION: There is provided an adhesive tape used for adhesion of an adherend containing a plasticizer and having an adhesive layer on one surface side of an air permeable substrate and an adhesive layer on the other surface side, where weight of total of the adhesive layer is in a range of 125 g/mto 175 g/m, gel fraction of the total of adhesive layer is 2 mass% to 35 mass% and the adhesive layer is an adhesive layer containing an acrylic polymer having a structure derived from a nitrogen-containing vinyl monomer.SELECTED DRAWING: None

Description

  The present invention relates to an adhesive tape that can be used for fixing a member containing a plasticizer.

  A plurality of conductive wires (wire harnesses) attached to automobiles, electronic devices, and the like are usually bound by a binding sheet made of a polyvinyl chloride sheet and an adhesive tape.

  As the binding sheet, specifically, a binding sheet in which an adhesive layer made of an aqueous adhesive composition containing a rubber latex and a tackifier resin emulsion is laminated on one side of a polyvinyl chloride sheet. Is known (for example, see Patent Document 1).

  However, since the polyvinyl chloride sheet usually contains a large amount of plasticizer, when the plasticizer moves to the adhesive layer over time, at the interface between the polyvinyl chloride sheet and the adhesive layer. There was a case of causing peeling. In particular, when a polyvinyl chloride sheet having a thickness of about 0.2 mm to 1 mm is folded in two or rolled, and the polyvinyl chloride sheet is bonded with an adhesive tape to bundle several wire harnesses. The transition of the plasticizer over time from the polyvinyl chloride sheet to the adhesive tape and the repulsive force of the polyvinyl chloride sheet slowly returning to the flat sheet state work on the adhesive tape over a long period of time. There has been concern about the possibility of problems such as unraveling of the binding.

JP 2007-211121 A

  The problem to be solved by the present invention is that, even when used for sticking an adherend containing a plasticizer, the sticking does not occur at the interface between the adherend and the pressure-sensitive adhesive layer. It is providing the adhesive tape which can hold | maintain over a long period of time.

  The present inventors consider that the peeling over time may be caused by the plasticizer moving to the pressure-sensitive adhesive layer and softening the pressure-sensitive adhesive layer, and the pressure-sensitive adhesive before the plasticizer is transferred It was examined to set the hardness of the layer higher in advance.

  However, in the pressure-sensitive adhesive layer, there are cases where the peeling with time cannot be effectively prevented. In particular, when the polyvinyl chloride sheet having a thickness of about 0.2 mm to 1 mm is folded in half or wound into a tubular shape, the polyvinyl chloride sheet is bonded with an adhesive tape to bundle several wire harnesses. There was a tendency to cause peeling over time. In addition, since the plasticizer is prevented from moving into the hard pressure-sensitive adhesive layer, it is concentrated on the interface between the polyvinyl chloride sheet and the pressure-sensitive adhesive layer, and is more likely to peel off at the interface. was there.

  Therefore, the present inventors have studied to further soften the pressure-sensitive adhesive layer before the plasticizer is transferred, and unexpectedly, when the range is set to a predetermined gel fraction range. The inventors have found that the peeling with time can be more effectively prevented.

That is, the present inventors are pressure-sensitive adhesive tapes used for sticking the adherend (a1) containing a plasticizer, and have a pressure-sensitive adhesive layer (b1) on one surface side of the gas-permeable substrate, It has the other pressure-sensitive adhesive layer on a surface side (b2), and, in the range basis weight of total of 125g ^{/ m 2} ~175g ^/ m 2 of the pressure-sensitive adhesive layer (b1) and the pressure-sensitive adhesive layer (b2) And the total gel fraction of the said adhesive layer (b1) and an adhesive layer (b2) is 2 mass%-35 mass%, It is related with the adhesive tape characterized by the above-mentioned.

  The pressure-sensitive adhesive tape of the present invention does not cause peeling at the interface between the adherend and the pressure-sensitive adhesive layer even when used for sticking an adherend containing a plasticizer. Can be held over.

The pressure-sensitive adhesive tape of the present invention has a pressure-sensitive adhesive layer (b1) on one side of a gas-permeable substrate, a pressure-sensitive adhesive layer (b2) on the other side, and the pressure-sensitive adhesive layer (b1). ) and it ranges basis weight of total of 125g ^{/ m 2} ~175g ^/ m 2 of the pressure-sensitive adhesive layer (b2), and a total gel fraction of the pressure-sensitive adhesive layer (b1) and the pressure-sensitive adhesive layer (b2) Is a pressure-sensitive adhesive tape having a content of 2% by mass to 35% by mass, and is used exclusively for attaching an adherend (a1) containing a plasticizer.

  The adhesive tape can be used for joining two or more adherends (a1) or joining an adherend other than the adherend (a1) and the adherend (a1).

  As said adhesive layer (b1) and adhesive layer (b2), the thing whose total gel fraction is the range of 2 mass%-35 mass% is used. Thereby, even if it is a case where the said plasticizer transfers to an adhesive layer (b1) etc., generation | occurrence | production of peeling with time can be prevented effectively. The gel fraction is preferably 2% by mass to 25% by mass, preferably 2% by mass to 15% by mass, and the plasticizer is an adhesive layer. Even in the case of shifting to (b1) or the like, it is more preferable for effectively preventing the occurrence of peeling over time.

  In addition, the use of the pressure-sensitive adhesive layer (b1) and the pressure-sensitive adhesive layer (b2) having a gel fraction in the above range allows the plasticizer to pass through the gas-permeable substrate so that the gas-permeable group is used. Since the adhesive layer (b1) and the adhesive layer (b2) provided on both sides of the material are relatively uniformly dispersed, the plasticizer is unevenly distributed at the interface between the adherend (a1) and the adhesive layer. As a result, interfacial peeling between the adherend (a1) and the pressure-sensitive adhesive layer can be effectively suppressed.

  The gel fraction was determined by immersing a pressure-sensitive adhesive tape whose mass of the pressure-sensitive adhesive layer was measured in advance for 72 hours in a mixed solvent of 70 parts by mass of toluene and 30 parts by mass of methanol adjusted to 23 ° C. Using an apparatus, after vibrating for 15 minutes at a frequency of 40 kHz in an atmosphere of 23 ° C., the mass after drying of the pressure-sensitive adhesive layer remaining in the mixed solvent and a value calculated based on the following equation are used.

Gel fraction (mass%) = {(mass of adhesive layer remaining in mixed solvent) / (mass of adhesive layer before immersion)} × 100
The mass of the pressure-sensitive adhesive layer constituting the pressure-sensitive adhesive tape before the immersion refers to a value obtained by subtracting the mass of the air-permeable substrate used for the production from the mass of the pressure-sensitive adhesive tape. Further, the mass of the remaining pressure-sensitive adhesive layer refers to a value obtained by subtracting the mass of the air-permeable substrate from the mass of the residue after drying.

  The gel fraction calculated by using the mixed solvent and applying ultrasonic vibration does not correlate with the gel fraction with respect to the solvent of toluene alone, but the intermolecular and intramolecular hydrogen of the pressure-sensitive adhesive layer. The apparent bond due to bonding or the like is divided, and the gel fraction resulting from the crosslinking reaction of a crosslinking agent or the like is indicated.

As the adhesive tape, to use those having the pressure-sensitive adhesive layer (b1) and an adhesive layer basis weight of the total is 125g ^{/ m 2} ~175g ^/ m 2 of the pressure-sensitive adhesive layer (b2). Thereby, when the plasticizer in the adherend (a1) moves to the pressure-sensitive adhesive layer provided on both surfaces of the gas-permeable substrate by passing through the gas-permeable substrate, the pressure-sensitive adhesive layer Since (b1) and the pressure-sensitive adhesive layer (b2) are relatively uniformly dispersed, it is possible to suppress the uneven distribution of the plasticizer at the interface between the adherend (a1) and the pressure-sensitive adhesive layer. It becomes possible to effectively suppress interfacial peeling between the adherend (a1) and the pressure-sensitive adhesive layer. Moreover, by using the pressure-sensitive adhesive layer having the basis weight in the above range, when the pressure-sensitive adhesive tape before being attached to the adherend (a1) is stored, the pressure-sensitive adhesive layer is prevented from protruding from the end. be able to. As the basis weight is ^preferably in the range of ^{135g / m 2 ~155g / m 2} , and more preferably in the range of ^{138g / m 2 ~145g / m 2} .

The total basis weight of the pressure-sensitive adhesive layer (b1) and the pressure-sensitive adhesive layer (b2) is the mass of the pressure-sensitive adhesive layer (b1) and the pressure-sensitive adhesive layer (b2) present per unit area (1 m ² ) of the pressure-sensitive adhesive tape. The value calculated based on the following formula is shown.

Total basis weight (g / m ² ) of the pressure-sensitive adhesive layer (b1) and pressure-sensitive adhesive layer (b2) = {(mass of pressure-sensitive adhesive layer (b1)) + (mass of pressure-sensitive adhesive layer (b2))} / (Area on one side of adhesive tape)
As the pressure-sensitive adhesive tape of the present invention, it is preferable to use a tape having a total thickness of 130 μm to 180 μm, and using a tape having a thickness of 140 μm to 150 μm can cause interfacial peeling between the adherend (a1) and the pressure-sensitive adhesive layer. It is more preferable for effectively suppressing the pressure-sensitive adhesive layer from protruding from the end during storage of the pressure-sensitive adhesive tape.

  The pressure-sensitive adhesive layer (b1) and the pressure-sensitive adhesive layer (b2) have a storage elastic modulus at 23 ° C. measured by a dynamic viscoelastic spectrum measured at a frequency of 1 Hz of 0.08 MPa to 0.12 MPa. It is preferable to use 0.08 MPa to 0.09 MPa, and it is possible to impart excellent adhesive force at the initial stage of application to the adherend (a1), and due to migration of the plasticizer It is more preferable because it can suppress a decrease in adhesive strength over time.

  The pressure-sensitive adhesive layer (b1) and pressure-sensitive adhesive layer (b2) have a ratio (tan δ) of loss elastic modulus to storage elastic modulus at 60 ° C. measured by a dynamic viscoelastic spectrum measured at a frequency of 1 Hz. It is preferable to use what is 0.40 to 0.60, and it is preferable to use what is 0.45 to 0.50 by using the adhesive tape bonded to the adherend (a1) at 60 ° C. When left in the environment, the plasticizer that can migrate from the adherend (a1) over time is not unevenly distributed at the adhesive interface with the adherend (a1), and has excellent adhesive force and cohesive force over a long period of time. It is more preferable when obtaining the adhesive tape to hold | maintain.

  The pressure-sensitive adhesive layer (b1) and the pressure-sensitive adhesive layer (b2) have a ratio of loss elastic modulus (tan δ) to storage elastic modulus at 100 ° C. measured by a dynamic viscoelastic spectrum measured at a frequency of 1 Hz. It is preferable to use what is 0.55-0.80, and it is preferable to use what is 0.60-0.70 for the said adhesive tape adhere | attached on the to-be-adhered body (a1) of 100 degreeC. When left in the environment, the plasticizer that can migrate from the adherend (a1) over time is not unevenly distributed at the adhesive interface with the adherend (a1), and has excellent adhesive force and cohesive force over a long period of time. It is more preferable when obtaining the adhesive tape to hold | maintain.

  The ratio (tan δ) is a value calculated based on the equation tan δ = loss elastic modulus (Pa) / storage elastic modulus (Pa).

  The storage elastic modulus at 23 ° C., and tan δ at 60 ° C. and 100 ° C. are measured using a viscoelasticity tester (trade name: ARES-G2 manufactured by TA Instruments Japan Co., Ltd.). Based on the storage elastic modulus measured at a frequency of 1 Hz under a temperature condition of 23 ° C., 60 ° C. or 100 ° C., and the storage elastic modulus and loss elastic modulus. Refers to the calculated value. In addition, as said test piece, what cut | judged the adhesive tape of this invention in the circular shape which consists of a magnitude | size of 2 mm in thickness and a diameter of 8 mm is used.

  The pressure-sensitive adhesive tape having the pressure-sensitive adhesive layer (b1) and the pressure-sensitive adhesive layer (b2) having a storage elastic modulus at 23 ° C. within the above range and tan δ of 60 ° C. and 100 ° C. is the repulsive force of the adherend (a1). The adherend (a1) caused by the migration of the plasticizer from the adherend (a1) to the pressure-sensitive adhesive layer even when left in an environment of 100 ° C. or less is unlikely to cause peeling. ) And the pressure-sensitive adhesive layer can be effectively suppressed.

  The said adhesive layer (b1) and an adhesive layer (b2) can be formed by using an adhesive, for example. Examples of the pressure-sensitive adhesive include acrylic pressure-sensitive adhesives, urethane-based pressure-sensitive adhesives, synthetic rubber-based pressure-sensitive adhesives, natural rubber-based pressure-sensitive adhesives, and silicone-based pressure-sensitive adhesives, and acrylic pressure-sensitive adhesives can be used. preferable.

  As said acrylic adhesive, what contains an acrylic polymer and a crosslinking agent, tackifying resin, etc. as needed can be used, and contains an acrylic polymer, a crosslinking agent, tackifying resin, etc. It is preferable to use an acrylic pressure-sensitive adhesive to obtain a pressure-sensitive adhesive tape having a pressure-sensitive adhesive layer excellent in weather resistance and heat resistance.

  As an acrylic polymer, what is obtained by superposing | polymerizing the monomer component containing a (meth) acryl monomer etc. can be used.

  Examples of the (meth) acrylic monomer include methyl (meth) acrylate, ethyl (meth) acrylate, n-butyl (meth) acrylate, isobutyl (meth) acrylate, t-butyl (meth) acrylate, and n-hexyl ( It has an alkyl group having 1 to 14 carbon atoms such as (meth) acrylate, n-octyl (meth) acrylate, isooctyl (meth) acrylate, isononyl (meth) acrylate, cyclohexyl (meth) acrylate, 2-ethylhexyl (meth) acrylate and the like. (Meth) acrylate can be used, and (meth) acrylate having an alkyl group having 4 to 9 carbon atoms is preferably used, and n-butyl acrylate or 2-ethylhexyl acrylate can be used alone or in combination. Even better Arbitrariness. After adhering to the surface of the adherend (a1) from the initial stage of application and exhibiting excellent adhesive force, and after the plasticizer migrates from the adherend (a1) to the pressure-sensitive adhesive layer over time, the adherend (a1 N-butyl having 4 carbon atoms, which is less affected by the steric hindrance of the alkyl group, in order to obtain a pressure-sensitive adhesive tape in which a plasticizer is not unevenly distributed at the adhesive interface and maintains excellent adhesive force and cohesive force over a long period of time. Most preferably, 60% by mass or more of acrylate is used.

  The (meth) acrylic monomer having an alkyl group having 1 to 14 carbon atoms is 80% by mass to 98.5% by mass with respect to the total amount of monomer components used for producing the acrylic polymer. It is preferable to use in the range, and it is more preferable to use in the range of 90% by mass to 98.5% by mass.

  As the (meth) acrylic monomer, it is preferable to use a highly polar monomer such as a highly polar vinyl monomer in addition to the above-described one.

  As the highly polar vinyl monomer, a (meth) acryl monomer having a carboxyl group, a nitrogen-containing vinyl monomer having an amino group or an amide group, or the like can be used alone or in combination.

  Of these, it is desirable to use a nitrogen-containing vinyl monomer in combination as the highly polar vinyl monomer.

  When the adherend (a1) is, for example, high-polarity polyvinyl chloride, a plasticizer that easily penetrates between the molecules of the polyvinyl chloride is used in order to more effectively plasticize the polyvinyl chloride. Often to do. Examples of the plasticizer include those having an aromatic ring and an ester group in the molecule. A plasticizer having a structure that is easily polarized between the aromatic ring and an ester group or the like easily enters between the molecules of the polyvinyl chloride.

  Here, when the acrylic polymer in the pressure-sensitive adhesive layers (b1) and (b2) has a carboxyl group, the carboxyl group has an extremely high polarity like the polyvinyl chloride. It becomes easy for the agent to penetrate into the molecule of the acrylic polymer contained in the pressure-sensitive adhesive layer, and as a result, the pressure-sensitive adhesive layer tends to be plasticized and its adhesive strength tends to be slightly reduced.

  Therefore, a pressure-sensitive adhesive layer containing an acrylic polymer using a nitrogen-containing vinyl monomer alone or in combination with a (meth) acrylic monomer having a carboxyl group is used as the highly polar vinyl monomer. Then, plasticization of the pressure-sensitive adhesive layer (b1) and the like by the plasticizer is more effectively suppressed, and as a result, excellent adhesive force can be maintained for a long time.

  Examples of the nitrogen-containing vinyl monomer include N-vinyl-2-pyrrolidone, N-vinylcaprolactam, acryloylmorpholine, dimethylaminoethyl acrylate, N, N-dimethylacrylamide, and N-isopropylacrylamide. The nitrogen-containing vinyl monomer is preferably 0.5% by mass to 20% by mass, and 0.8% by mass to 10% by mass with respect to the total amount of monomer components used for the production of the acrylic polymer. % Is more preferable, and 1.0 mass% to 2.5 mass% is further more preferable. 1.0 mass%-1.9 mass% is the most preferable.

  By adjusting the structural ratio derived from the nitrogen-containing vinyl monomer constituting the acrylic polymer within the above range, the acrylic pressure-sensitive adhesive layer is appropriately softened, and from the initial stage of application to the surface of the adherend (a1). Familiarly, after exhibiting excellent adhesive force and the plasticizer transferred from the adherend (a1) to the pressure-sensitive adhesive layer over time, the plasticizer is not unevenly distributed on the adherend (a1) and the adhesive interface, It is possible to obtain a pressure-sensitive adhesive tape that retains excellent adhesive force and cohesive force over a long period of time.

  The vinyl monomer having a carboxyl group is preferably used in the range of 0.2% by mass to 5% by mass with respect to the total amount of the monomer component, and 0.4% by mass to 3% by mass. It is more preferable to use within a range. Most preferably, it is used in the range of 1.5% by mass to 2.5% by mass. When the amount of the vinyl monomer having a carboxyl group is within the above range, an excellent adhesive force can be exhibited from the initial stage of application to a highly polar adherend (a1) such as a polyvinyl chloride resin.

  Since the carboxyl group is highly polar as described above, if it is present in a large amount in the pressure-sensitive adhesive layer (b1) or the like, a pressure-sensitive adhesive layer that is easily plasticized by the plasticizer derived from the adherend (a1) is formed. There is a case. Therefore, use of the vinyl monomer having a carboxyl group within the above-described range suppresses the penetration of the plasticizer into the pressure-sensitive adhesive layer (b1) and the like, and the adhesive force due to the influence of the plasticizer. It is preferable for obtaining a pressure-sensitive adhesive tape that is less deteriorated and retains excellent adhesive strength and cohesive strength over a long period of time.

  Examples of the highly polar vinyl monomer include monomers having a sulfonic acid group such as vinyl acetate, ethylene oxide-modified succinic acid acrylate, 2-acrylamido-2-methylpropanesulfonic acid, 2-methoxy, in addition to those described above. Other highly polar vinyl monomers such as terminal alkoxy-modified (meth) acrylates such as ethyl (meth) acrylate and 2-phenoxyethyl (meth) acrylate can be used.

  The other highly polar vinyl monomer is preferably used in a range of 0.2% by mass to 5% by mass with respect to the total amount of the monomer components, and in a range of 0.4% by mass to 3% by mass. More preferably it is used. Most preferably, it is used in the range of 2.0 mass% to 3.0 mass%. When the amount of the other highly polar vinyl monomer used is in the above range, the adhesion to the surface of the highly polar adherend (a1) such as polyvinyl chloride resin is increased from the initial stage of application, and the carboxyl group Since the plasticizer does not have the same polarity as that of the vinyl monomer having an adhesive, it is difficult for the plasticizer to enter between the molecules of the acrylic polymer, and the plasticizer moves from the adherend (a1) to the adhesive layer over time. However, it is possible to obtain a pressure-sensitive adhesive tape that retains excellent adhesive strength and cohesive strength over a long period of time.

  As the monomer that can be used for the production of the acrylic polymer, those having a functional group capable of reacting with a crosslinking agent described later can be used. For example, a (meth) acrylic monomer having a hydroxyl group is used. be able to.

  Examples of the (meth) acrylic monomer having a hydroxyl group include 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 4-hydroxybutyl (meth) acrylate, and 6-hydroxyhexyl (meth). Acrylate or the like can be used.

  The (meth) acrylic monomer having a hydroxyl group is preferably used in the range of 0.05% by mass to 2.0% by mass with respect to the total amount of the monomer component, and 0.1% by mass to 0%. More preferably, it is used in the range of 0.5% by mass, and 0.1% by mass to 0.2% by mass has the gel fraction of the pressure-sensitive adhesive layer (b1) and the pressure-sensitive adhesive layer (b2) in the above-mentioned range. It is easy to adjust, and as a result, it adapts to the surface of the adherend (a1) from the initial stage of application, exhibits an excellent adhesive force, and the plasticizer moves from the adherend (a1) to the adhesive layer over time. The cross-linked structure between the acrylic polymers does not inhibit the fluidity of the plasticizer and can suppress the uneven distribution of the plasticizer at the adhesive interface with the adherend (a1). An adhesive tape that retains force can be obtained.

  The acrylic polymer can be produced by polymerizing the monomer component by a known method such as a solution polymerization method, a bulk polymerization method, a suspension polymerization method, or an emulsion polymerization method, and is produced by a solution polymerization method. It is preferable to improve the production efficiency of the pressure-sensitive adhesive tape and reduce the production cost.

  As the acrylic polymer, those having a weight average molecular weight in the range of 300,000 to 1,500,000 are preferably used, and those having a weight average molecular weight in the range of 500,000 to 1,000,000 are preferably used.

The weight average molecular weight can be measured by gel permeation chromatograph (GPC). More specifically, as a GPC measurement device, “SC8020” manufactured by Tosoh Corporation can be used to measure and obtain the following GPC measurement conditions based on polystyrene conversion values.
(GPC measurement conditions)
Sample concentration: 0.5% by mass (tetrahydrofuran solution)
Sample injection volume: 100 μL
・ Eluent: Tetrahydrofuran (THF)
・ Flow rate: 1.0 mL / min
Column temperature (measurement temperature): 40 ° C
Column: “TSKgel GMHHR-H” manufactured by Tosoh Corporation
・ Detector: Differential refraction

  As the pressure-sensitive adhesive that can be used for forming the pressure-sensitive adhesive layer (b1) and the pressure-sensitive adhesive layer (b2), it is preferable to use a material containing a crosslinking agent in addition to the acrylic polymer. By using the one containing the cross-linking agent, the adhesive strength to the surface of the adherend (a1) is excellent from the initial stage of application, and after the plasticizer is transferred from the adherend (a1) to the pressure-sensitive adhesive layer over time, it is long. A pressure-sensitive adhesive tape that retains excellent adhesive force and cohesive force over a period of time can be obtained.

  Examples of the crosslinking agent include isocyanate crosslinking agents, epoxy crosslinking agents, chelate crosslinking agents, aziridine crosslinking agents, oxazoline crosslinking agents, and the like, depending on the type of crosslinking functional group that the acrylic polymer has. Can be selected and used. The content of the crosslinking agent is preferably 0.3 parts by mass to 1.8 parts by mass, more preferably 0.6 parts by mass to 1.3 parts by mass with respect to 100 parts by mass of the acrylic polymer. 6 parts by mass to 0.9 parts by mass are most preferable.

  The content of the crosslinking agent can be appropriately selected and used so that the pressure-sensitive adhesive layer (b1) and the pressure-sensitive adhesive layer (b2) having the gel fraction can be formed.

  In order to further improve the adhesive force of the pressure-sensitive adhesive tape, the pressure-sensitive adhesive may contain a tackifier resin.

  As the tackifying resin, rosin resin, terpene resin, aliphatic (C5) or aromatic (C9) petroleum resin, styrene resin, phenol resin, xylene resin, methacrylic resin, etc. are used. can do. Among these, as the tackifier resin, it is preferable to use a rosin resin, and it is preferable to use a polymerized rosin resin.

  The tackifying resin is preferably used in an amount of 5 to 50 parts by weight, preferably 10 to 30 parts by weight, based on 100 parts by weight of the acrylic polymer, and is initially applied to the adherend (a1). It is more preferable because excellent adhesive strength can be imparted and a decrease in the adhesive strength over time due to the migration of the plasticizer can be suppressed.

  As an embodiment of the pressure-sensitive adhesive tape of the present invention, a pressure-sensitive adhesive tape having the pressure-sensitive adhesive layer (b1) and the pressure-sensitive adhesive layer (b2) on both sides of a gas-permeable substrate (core) can be mentioned.

  The pressure-sensitive adhesive tape of the present invention includes, for example, a step of forming the pressure-sensitive adhesive layer (b1) and the pressure-sensitive adhesive layer (b2) by coating the pressure-sensitive adhesive on the surface of a release liner and drying, for example. Can be manufactured through a step of transferring to the both sides of the air-permeable substrate.

(Air-permeable substrate)
As the gas permeable substrate, it is possible to use a material in which the plasticizer is transferred from the adherend (a1) to the pressure-sensitive adhesive layer, and then the plasticizer can pass through the gas permeable substrate (core). It is preferable for effectively suppressing interfacial peeling between the adherend (a1) and the pressure-sensitive adhesive layer in contact therewith.

  As the air permeable base material, a test piece is formed by laminating 10 air permeable base materials, and the Gurley type air permeability measured in accordance with JISP 8117 of the test piece is 0.35 sec / 100 ml or less. It is preferable to use those in the range of 0.05 seconds / 100 ml to 0.3 seconds / 100 ml, more preferably in the range of 0.1 seconds / 100 ml to 0.2 seconds / 100 ml. Is used, the plasticizer is relatively uniformly dispersed in the entire pressure-sensitive adhesive layer formed on both surfaces of the gas-permeable substrate. As a result, the adherend (a1) and the pressure-sensitive adhesive layer in contact with the adherend (a1) Can be effectively suppressed.

  The Gurley-type air permeability is an air permeability measured in accordance with JIS P8117 using 10 air permeable base materials stacked and 10 base materials as a test piece. Measurement is performed when 10 core substrates are stacked and set in 23 ° C. and 50% RH, and an inner tube with an inner diameter of 28.6 mm and a weight of 567 g is dropped and 100 ml of air is measured. Measure the transit time.

  As the gas permeable substrate, one having a thickness of 10 μm to 50 μm, preferably 20 μm to 45 μm is used. The pressure-sensitive adhesive layer (b1) and the pressure-sensitive adhesive layer (b2) have been impregnated into the pores of the gas-permeable base material and have migrated from the adherend (a1) by using the gas-permeable base material having the thickness. Since the plasticizer is allowed to pass through, it is possible to suppress the uneven distribution of the plasticizer in the pressure-sensitive adhesive layer (b1) and the pressure-sensitive adhesive layer (b2), and to obtain a pressure-sensitive adhesive tape that maintains excellent adhesive force and cohesive force over a long period of time. be able to. Furthermore, the pressure-sensitive adhesive layer (b1) and the pressure-sensitive adhesive layer (b2) are impregnated into the pores of the gas-permeable substrate by using the gas-permeable substrate having the thickness, and the tensile strength of the gas-permeable substrate is increased. Thus, an adhesive tape excellent in handling workability in the cutting process and the sticking process can be obtained.

  As the air permeable substrate, it is preferable to use a nonwoven fabric substrate or a porous film substrate because it is easy to ensure the air permeability in the above range. Specific examples of the gas permeable substrate include a nonwoven fabric substrate, a woven fabric substrate, and a fiber woven fabric (mesh substrate) composed of monofilament yarn. It is preferable to use a non-woven fabric base material that easily obtains the rate and a mesh base material that easily obtains a high Gurley air permeability.

  As a material of the nonwoven fabric substrate, a known and conventional nonwoven fabric used as a nonwoven fabric for pressure-sensitive adhesive tapes can be used. Typical examples include hemp such as Manila hemp, cellulosic fibers such as rayon, regenerated cellulose, and wood pulp, chemical fibers such as acetate fiber, polyester fiber, polyvinyl alcohol fiber, polyamide fiber, and mixtures thereof. Furthermore, you may perform the impregnation process which used the viscose impregnation and the thermoplastic resin as a binder as needed.

  For the purpose of improving the strength of the nonwoven fabric, it is preferable to add a known and usual reinforcing agent in the nonwoven fabric manufacturing process. As the reinforcing agent, an internal additive reinforcing agent or an external additive reinforcing agent may be used alone or in combination. As the internal reinforcement, polyacrylamide resins, urea-formaldehyde resins, melamine-formaldehyde resins, epoxy-polyamide resins, and the like can be used. In particular, a polyamidoamine / epichlorohydrin resin which is an epoxy-polyamide resin is preferable because it significantly increases the interlayer strength of the nonwoven fabric. The amount of the internally added reinforcing agent is preferably 0.2 to 1% by mass, more preferably 0.3 to 0.5% by mass, based on the nonwoven fabric. On the other hand, as the external additive reinforcing agent, a thermoplastic resin such as starch; viscose, carboxymethylcellulose, polyvinyl alcohol, polyacrylamide or the like can be used. Especially, in order to raise the interlayer strength of a nonwoven fabric base material, it is preferable to use the above-mentioned internal additive reinforcement agent.

The basis weight of the nonwoven fabric base material is preferably 5 to 15 g / ^{m 2,} and still more preferably 7~12g / ^{m 2.} The density of the nonwoven fabric base material is preferably 0.15~0.35g / ^{m 3,} more preferably 0.2 to 0.3 g / ^{m 3.} The pressure-sensitive adhesive layer (b1) and the pressure-sensitive adhesive layer (b2) are impregnated into the pores of the nonwoven fabric base and have migrated from the adherend (a1) when the basis weight range of the nonwoven fabric base is within the range. Since the plasticizer is allowed to pass through, it is possible to suppress the uneven distribution of the plasticizer in the pressure-sensitive adhesive layer (b1) and the pressure-sensitive adhesive layer (b2), and to obtain a pressure-sensitive adhesive tape that maintains excellent adhesive force and cohesive force over a long period of time. Can do. Furthermore, by using the nonwoven fabric substrate having the basis weight, the pressure-sensitive adhesive layer (b1) and the pressure-sensitive adhesive layer (b2) impregnate the pore portions of the substrate, and the tensile strength of the nonwoven fabric substrate is improved. The handling workability in the cutting step and the pasting step can be improved.

  The paper making method of the nonwoven fabric substrate is not particularly limited, but can be obtained by a known wet method, using a circular net paper machine, a short net paper machine, a long net paper machine, an inclined short net paper machine, etc. Various papermaking methods are used.

  As the porous film base material, a mesh base material in which known monofilament fibers such as polyester resin, amide resin, polyarylate resin or the like are woven in a screen shape can be used. Among them, it is preferable to use a polyester resin having a high tensile elastic modulus and high tensile strength as a monofilament. As a form of the mesh substrate, a mesh substrate having a thickness of 10 to 50 μm in which 80 to 300 monofilament yarns having a fiber diameter of 5 to 25 μm are alternately woven by MD and TD per inch is used. Preferably, it is a mesh substrate having a thickness of 10 to 50 μm in which 100 to 200 monofilament yarns having a fiber diameter of 5 to 25 μm are alternately woven in MD and TD per inch. When the fiber diameter is within the mesh base, the pressure-sensitive adhesive layer (b1) and the pressure-sensitive adhesive layer (b2) are impregnated into the pores of the base material, and the plastic that has migrated from the adherend (a1) Since the agent is allowed to pass through, it is possible to suppress the uneven distribution of the plasticizer in the pressure-sensitive adhesive layer (b1) and the pressure-sensitive adhesive layer (b2), and to obtain a pressure-sensitive adhesive tape that maintains excellent adhesive force and cohesive force over a long period of time. it can. Furthermore, by using the mesh base material having the thickness, the pressure-sensitive adhesive layer (b1) and the pressure-sensitive adhesive layer (b2) are impregnated into the pores of the base material, and the tensile strength of the mesh base material is improved. The handling workability in the cutting step and the pasting step can be improved.

  In the pressure-sensitive adhesive tape of the present invention obtained by the above method, a release liner may be laminated on the pressure-sensitive adhesive layer (b1) and the pressure-sensitive adhesive layer (b2). Examples of the release liner include papers such as kraft paper, glassine paper, and high-quality paper, polyethylene, polypropylene (orientated polypropylene (OPP), cast polypropylene (CPP)), resin films such as polyethylene terephthalate, and the papers. Laminated paper laminated with a resin film, paper that has been sealed with clay, polyvinyl alcohol, or the like on the paper, or the like that has one or both sides peeled off with a silicone resin or the like can be used. .

(Adherent (a1))
As the adherend (a1), for example, one containing a plasticizer and polyvinyl chloride, or a plasticizer and rubber can be used.

  Examples of the plasticizer include aliphatic esters such as di-2-ethylhexyl phthalate, diisononyl phthalate, diisodecyl phthalate, phosphate esters such as trioctyl phosphate, dioctyl adipate, diisononyl adipate, and diisodecyl adipate. Illustrative examples include trimellitic acid esters such as dibasic acid esters and trimellitic acid tri-2-ethylhexyl, and epoxy plasticizers such as butyl epoxy stearate. Two or more kinds of the plasticizers may be combined. The pressure-sensitive adhesive tape of the present invention is preferably used for an adherend containing a phthalate ester as the plasticizer, and is preferably used for an adherend containing diisononyl phthalate. Since the plasticization of the sheet can be efficiently performed, the polyvinyl chloride sheet can be plasticized with a small amount of addition, and the decrease in the adhesive force due to the plasticizer can be effectively prevented, which is more preferable.

  As content of the said plasticizer, it is preferable to contain the plasticizer of the range of 15 mass%-30 mass% with respect to the mass of the said adherend (a1), and the mass of the said adherend (a1) is included. On the other hand, it is more preferable to contain a plasticizer in the range of 20% by mass to 26% by mass. The adherend (a1) having a plasticizer content within the above range has sufficient flexibility to bundle the wire harness even in a low temperature environment of about 5 ° C. or less, and adheres from the adherend. The amount of plasticizer transferred to the tape is also preferable because it is more effectively suppressed.

  As the adherend (a1) containing the plasticizer, an inorganic filler such as calcium carbonate, talc, calcined clay, kaolin, aluminum hydroxide, titanium oxide or the like is provided in order to impart moderate impact resistance according to the application. Or you may contain the organic pigment for coloring. The amount of the inorganic additive used is preferably 10% by mass to 60% by mass with respect to the mass of polyvinyl chloride or rubber, and 20% by mass to 40% by mass is excellent in impact resistance and wire. A sufficient level of flexibility to bundle the harness can be achieved. Carbon black or the like can be used as the organic pigment. The amount of the organic pigment used is in the range of 2% by mass to 10% by mass with respect to the mass of polyvinyl chloride or rubber, so that good impact resistance and flexibility can be maintained.

  The thickness of the adherend (a1) containing the plasticizer is preferably 0.2 mm to 1 mm, and 0.3 mm to 0.5 mm is flexible enough to bundle the wire harness. It is more preferable because the adherend (a1) is not easily stretched when the wire harness is bent, and the binding of the wire harness is difficult to loosen. Moreover, the surface of the adherend (a1) containing the plasticizer may have an embossed pattern or the like as necessary. The said embossed pattern can be provided in the surface by letting a to-be-adhered body (a1) pass between the metal nip rolls heated at 80 degreeC or more.

  The adherend (a1) containing the plasticizer is formed into a sheet shape by any film forming method such as T-die extrusion molding, calendar molding, inflation molding, etc., in a state where the resin compound is melted at a high temperature. can do.

(Wire harness binding sheet)
The pressure-sensitive adhesive tape of the present invention obtained by the above method can be used for bonding and fixing a sheet for bundling two or more wire harnesses used in, for example, vehicles. For example, the sheet is continuously bonded to one end of a long adherend (a1) slit in a roll having a width of 50 mm, in the flow direction, and bonded to a wire harness. It becomes a sheet.

  In order to evaluate the peeling resistance due to the migration of the plasticizer during storage in stock, the sheet can be left, for example, under wet heat conditions of 60 ° C. and 80% RH for several days. As wet heat conditions, it is preferable to leave the substrate at a temperature equal to or lower than the softening temperature of the adherend (a1). Specifically, it is preferable to stand for 3 days to 10 days at a temperature of 40 ° C. to 70 ° C. and a humidity of 70% to 90% RH. When the moisture and heat conditions are within the above range, the adherend (a1) is less likely to be thermally deformed, and a rapid transition of the plasticizer can be suppressed. Easy to disperse uniformly.

  The sheet to which the adherend (a1) and the pressure-sensitive adhesive tape are stuck is attached to one end of the same sheet surface to which the pressure-sensitive adhesive tape is not stuck, while wrapping two or more wire harnesses in the center. Two or more wire harnesses can be bundled by combining them or by sticking them to one end of the back surface in a roll shape.

  As a method for confirming uniform dispersion after the migration of the plasticizer into the pressure-sensitive adhesive layer, for example, diisononyl phthalate is used as the plasticizer, and the pressure-sensitive adhesive layer (b1) and the pressure-sensitive adhesive layer (b2) are formed. The value measured by the method of the following (1)-(3) is pointed out for the case where an acrylic adhesive is used as an adhesive used for A.

(1) Preparation of calibration curve A pressure-sensitive adhesive layer is formed by applying and drying a pressure-sensitive adhesive in which 10 parts by mass of a plasticizer is uniformly added to 100 parts by mass of the solid content of the acrylic pressure-sensitive adhesive and drying it. Then, the adhesive tape (C1) is prepared by transferring it onto both surfaces of the nonwoven fabric substrate.

  Next, an acrylic pressure-sensitive adhesive without adding a plasticizer is applied to the surface of the release liner and dried to form a pressure-sensitive adhesive layer, which is then transferred to both sides of the nonwoven fabric base material, thereby giving a pressure-sensitive adhesive tape (C0). Create

  Next, the infrared absorption spectrum of the pressure-sensitive adhesive layer surface of the pressure-sensitive adhesive tape (C1) is measured by the ATR method to obtain an infrared absorption spectrum (D1).

  Next, the infrared absorption spectrum of the pressure-sensitive adhesive layer surface of the pressure-sensitive adhesive tape (C0) is measured by the ATR method to obtain an infrared absorption spectrum (D0).

  Next, the infrared absorption spectrum (E1) of the plasticizer is extracted by subtracting the infrared absorption spectrum (D0) from the infrared absorption spectrum (D1) (difference spectrum).

From the infrared absorption spectrum (E1), the height (F1) of the absorption peak at 1285 cm ⁻¹ derived from the plasticizer is measured.

Next, the infrared absorption spectrum of the pressure-sensitive adhesive layer surface of the pressure-sensitive adhesive tape (C1) is measured by the ATR method to obtain an infrared absorption spectrum (D1). Next, the height (G1) of the absorption peak at 1160 cm ⁻¹ derived from the acrylic polymer is measured from the infrared absorption spectrum (D1).

  Next, an acrylic adhesive in which 20 parts by mass of a plasticizer is added to 100 parts by mass of a solid content of the acrylic adhesive, an acrylic adhesive in which 30 parts by mass of a plasticizer is added, and 40 parts by mass of a plasticizer Each of the added acrylic pressure-sensitive adhesives is prepared, and each pressure-sensitive adhesive is applied to the surface of the release liner and dried to form a pressure-sensitive adhesive layer. Make an adhesive tape.

Next, the infrared absorption spectrum of the adhesive layer surface of the four types of adhesive tapes is measured by the ATR method. From the four types of infrared absorption spectra, the height of the absorption peak at 1285 cm ⁻¹ derived from the plasticizer and the height of the absorption peak at 1160 cm ⁻¹ derived from the acrylic polymer are measured.

The vertical axis represents the plasticizer addition amount [parts by mass] added to 100 parts by mass of the solid content of the acrylic pressure-sensitive adhesive, and the horizontal axis represents the height of the absorption peak at 1160 cm ⁻¹ derived from the acrylic polymer ( The ratio (F1 / G1) of the height (F1) of the absorption peak of 1285 cm ⁻¹ derived from the plasticizer relative to G1), and the ratio of the plasticizer contained in the four types of adhesive tapes and the ratio (F1 / A value corresponding to G1) is plotted to create a calibration curve.

  In addition, the said infrared absorption spectrum is measured using a Fourier-transform infrared spectrophotometer (JASCO Corporation FT / IR-4100).

(2) Measurement of the amount of plasticizer on the surface of the pressure-sensitive adhesive layer After removing the release liner from the surface of the pressure-sensitive adhesive layer (b1) of any pressure-sensitive adhesive tape, it is pasted on the adherend (a1) containing the plasticizer. The adhesive tape (C2) is obtained by allowing it to stand for 9 days in wet heat conditions such as 80 ° C. and 80% RH.

Next, the release liner is removed from the surface of the pressure-sensitive adhesive layer (b2) of the pressure-sensitive adhesive tape (C2), and the infrared absorption spectrum (D2) of the surface of the pressure-sensitive adhesive layer (b2) is measured by the ATR method. based on the external absorption spectrum (D2), the ratio of the height of the absorption peak of 1285 ^-1 derived from the plasticizer (F2) and the height of the absorption peak of 1160 cm ^-1 derived from the acrylic polymer (G2) (F2 / G2) is obtained.

  Next, F2 / G2 is applied to the horizontal axis of the calibration curve, and the content (H2) [part by mass] of the plasticizer contained in the adhesive layer (b2) of the adhesive tape (C2) is calculated. . The content of the plasticizer indicates the migration amount [parts by mass] of the plasticizer that has migrated from the polyvinyl chloride sheet when the pressure-sensitive adhesive layer (b2) excluding the plasticizer is 100 parts by mass. .

  Next, the pressure-sensitive adhesive layer (b1) in contact with the adherend (a1) is peeled off, and the plasticizer content (J2) [parts by mass] contained in the surface of the pressure-sensitive adhesive layer (b1) Calculate in the same way.

(3) Evaluation of Uniform Dispersibility of Plasticizer The uniform dispersibility of the plasticizer is based on the difference between the plasticizer content (H2) obtained by the method and the plasticizer content (J2). If the difference between the content (H2) and the content (J2) is in the range of ± 2 parts by mass, it can be evaluated as an adhesive tape excellent in uniform dispersibility of the plasticizer. it can.

  The amount of plasticizer transferred from the adherend (a1) to the pressure-sensitive adhesive layer (b1) and pressure-sensitive adhesive layer (b2) constituting the pressure-sensitive adhesive tape is preferably 0 to 35 parts by weight, and 0 parts by weight. -20 mass parts is more preferable. If the amount of migration of the plasticizer is within 35 parts by mass, the plasticizer can be dispersed relatively uniformly in the pressure-sensitive adhesive layer (A), so that the plasticizer is bonded to the adherend (a1) and the pressure-sensitive adhesive layer ( Adhesion with A) is not inhibited and good peeling resistance can be maintained.

(T-peel adhesive strength)
An adhesive tape from which the release liner was removed from the adhesive layer (b1) was affixed to the adherend (a1-1) and cut into a 15 mm width and a 100 mm length as a test piece. The test piece was left for 9 days under wet heat conditions such as 60 ° C. and 80% RH. Further, the adherend (a1-2) to which the adhesive tape was not attached was cut into a width of 15 mm and a length of 100 mm and left under the same conditions as the test piece.

  After the standing, the test piece and the adherend (a1-2) are taken out in an atmosphere of 23 ° C. and 50% RH, and the release liner is peeled off from the pressure-sensitive adhesive layer (b2) of the test piece. The adherend (a1-2) was applied, the 2 kg roller was reciprocated once, and left in the same atmosphere for 30 minutes to adhere them.

  One end of the adherend (a1-2) is fixed to the lower chuck of the tensile device of the Tensilon tensile tester, and the adherend (a1-1) is attached to the upper chuck of the tensile device of the Tensilon tensile tester. The adhesive strength (T-peel adhesive strength) was measured by fixing and pulling the upper chuck at a speed of 3 mm / min.

  It was judged that the higher the numerical value, the better the peel resistance in holding the wire harness in a bundle. The range of the adhesive force is preferably 1.5 N / 15 mm or more, and more preferably 2.0 N / 15 mm or more. Moreover, it is preferable that the pressure-sensitive adhesive layer cohesively breaks when measuring the adhesive force. When peeling off at the interface between the adherend (a1-1) and the adhesive tape, the plasticizer transferred from the adherend (a1-1) is the adherend (a1) and the adhesive layer (b1). And the cohesive failure indicates that the plasticizer is uniformly dispersed in the pressure-sensitive adhesive layer (b1) and the pressure-sensitive adhesive layer (b2). It can be said that it is shown.

  Examples will be described in detail below.

Example 1
(1-1) Preparation of acrylic pressure-sensitive adhesive composition (S) In a reaction vessel equipped with a stirrer, a reflux condenser, a nitrogen inlet tube, and a thermometer, 93.4 parts by mass of butyl acrylate, 3 parts by mass of vinyl acetate, acrylic 2.5 parts by weight of acid, 1 part by weight of N-vinyl-2-pyrrolidolin, 0.1 part by weight of 2-hydroxyethyl acrylate, and 0.2 part by weight of 2,2′-azobisisobutylnitrile as a polymerization initiator The resultant was dissolved in 100 parts by mass of ethyl acetate and polymerized at 80 ° C. for 8 hours to obtain an acrylic polymer solution having a weight average molecular weight of 700,000. 15 parts by mass of rosin ester-based resin A-100 (manufactured by Arakawa Chemical Co., Ltd.) as a tackifying resin and 100% by mass of the acrylic polymer (solid content), polymerized rosin ester-based resin D-135 (Arakawa Chemical Industries) 15 parts by mass) was added and diluted with toluene to obtain an acrylic pressure-sensitive adhesive composition (S) having a nonvolatile content of 40% by mass.

(1-2) Double-sided adhesive tape S-1
0.52 parts by mass of an isocyanate-based crosslinking agent (manufactured by Tosoh Corporation, Coronate L-45E, solid content 45% by mass) is added to 100 parts by mass of the acrylic pressure-sensitive adhesive composition (S), and 15 parts by a dissolver stirrer. After stirring for a minute, the pressure-sensitive adhesive layer was applied to the release liner with a roll coater so that the basis weight after drying was 69 g / m ² and dried in an 85 ° C. dryer for 3 minutes. The content of the crosslinking agent (solid content) with respect to 100 parts by mass of the acrylic polymer (solid content) was 0.76 parts by mass.

According to the above method, two pressure-sensitive adhesive layers were prepared, which were laminated on both sides of a 43 μm-thick nonwoven fabric A (Nippon Paper Papillia, No. 1215) and heated to 100 ° C. (manufactured by Tester Sangyo Co., Ltd.) SA-1010, a small tabletop test laminator) was applied at a rate of 1 m / min while applying a pressure of 0.4 MPa, and then cured for 48 hours in a dryer at 40 ° C., thereby being provided on both sides of the nonwoven fabric. A double-sided pressure-sensitive adhesive tape having a total basis weight of the pressure-sensitive adhesive layer of 138 g / m ² , a gel fraction of the pressure-sensitive adhesive layer of 10% by mass and a thickness of 145 μm was prepared. The nonwoven fabric No. The Gurley air permeability of 1215 was 0.2 seconds / 100 ml.

(Example 2)
(2-1) Double-sided adhesive tape S-2
Except having changed the usage-amount of the isocyanate type crosslinking agent (The Tosoh Corporation make, Coronate L-45E, solid content 45 mass%) from 0.52 mass part to 0.39 mass part, it carried out similarly to Example 1. Double-sided adhesive tape S-2 was obtained. The gel fraction of the pressure-sensitive adhesive layer was 2% by mass. The content of the crosslinking agent (solid content) with respect to 100 parts by mass of the acrylic polymer (solid content) was 0.57 parts by mass.

(Example 3)
(3-1) Double-sided adhesive tape S-3
Except having changed the usage-amount of the isocyanate type crosslinking agent (the Tosoh Corporation make, Coronate L-45E, solid content 45 mass%) from 0.52 mass part to 0.71 mass part, it carried out similarly to Example 1. Double-sided adhesive tape S-3 was obtained. The gel fraction of the pressure-sensitive adhesive layer was 30% by mass. The content of the crosslinking agent (solid content) with respect to 100 parts by mass of the acrylic polymer (solid content) was 1.04 parts by mass.

Example 4
(4-1) Preparation of acrylic pressure-sensitive adhesive composition (T) In a container, 75 g of deionized water and Aqualon KH-1025 [Daiichi Kogyo Seiyaku Co., Ltd .; active ingredient 25% by mass] as a surfactant are 20 mass. Part and 37.5 parts by mass of Latemul PD-104 [manufactured by Kao Corporation; active ingredient 20% by mass], which is a surfactant, were uniformly dissolved. There, 227.5 parts by weight of n-butyl acrylate, 227.5 parts by weight of 2-ethylhexyl acrylate, 25 parts by weight of methyl methacrylate, 6 parts by weight of N-vinyl-2-pyrrolidone, 4 parts by weight of acrylic acid, 10 parts by weight of methacrylic acid And 0.2 part by mass of lauryl mercaptan as a chain transfer agent was added and emulsified to obtain an emulsion (1) 632.7 parts by mass.

  A reaction vessel equipped with a stirrer, reflux condenser, nitrogen inlet tube, thermometer, and dropping funnel was charged with 333.35 parts by mass of deionized water and heated to 60 ° C. while blowing nitrogen. Under stirring, a part of emulsion (1) 7.59 parts by mass, aqueous ammonium persulfate solution 2.5 parts by mass [active ingredient 6% by mass], sodium hydrogen sulfite aqueous solution 2.5 parts by mass [active ingredient 2% by mass] The polymer was added and polymerized in 1 hour while maintaining 60 ° C.

  Next, 625.11 parts by mass of the remaining emulsion (1) and 50 parts by mass of an aqueous solution of ammonium persulfate [active ingredient 1% by mass] were used for 6 hours while keeping the reaction vessel at 60 ° C. using separate funnels. The polymerization was conducted dropwise.

  Next, using a separate funnel, 2.5 parts by mass of an aqueous ammonium persulfate solution [active ingredient 6% by mass] and 2.5 parts by mass of an aqueous sodium hydrogen sulfite solution 2% by mass are used to bring the reaction vessel to 60 ° C. It was dripped over 1 hour, keeping.

  After completion of dropping, the reaction vessel was stirred for 1 hour while maintaining the temperature at 60 ° C., and then the contents were cooled and adjusted with ammonia water [10% by mass of active ingredient] so that the pH was 7.2. This was filtered through a 200-mesh wire mesh to obtain an acrylic polymer emulsion (1). Here, the obtained acrylic polymer emulsion (1) had a solid content concentration of 50 mass%, an average particle size of 333 nm, and a weight average molecular weight of 800,000.

  Epocross WS-700 [manufactured by Nippon Shokubai Co., Ltd., water-soluble type, nonvolatile content 25 mass%, oxazoline group amount 4.5 mmol / g (solid) to 1000 parts by mass of the acrylic polymer emulsion (1) ] 25 parts by mass, superester E-865NT which is an emulsion type polymerized rosin ester-based tackifier resin as a tackifier resin [Arakawa Chemical Industries, Ltd .; softening point 160 ° C., solid content 50% by mass] 200 parts by mass, leveling Surfinol PSA-336 [manufactured by Air Products Japan Co., Ltd.] 2.5 parts by mass as an agent, Surfinol DF-110D [manufactured by Air Products Japan Ltd.] 2.5 parts by mass as an antifoaming agent did. After stirring uniformly, it was filtered through a 200 mesh wire mesh. The acrylic pressure-sensitive adhesive composition (T) was obtained by curing for 30 days in a 23 ° C. environment. The content of the crosslinking agent (solid content) with respect to 100 parts by mass of the acrylic polymer (solid content) was 1.28 parts by mass.

(4-2) Double-sided adhesive tape T-1
The total basis weight of the pressure-sensitive adhesive layer provided on both sides of the nonwoven fabric was 130 g, as in Example 1, except that the release liner was coated with a roll coater so that the basis weight after drying was 65 g / m ^2. / M ^2, a double-sided pressure-sensitive adhesive tape T-1 having ^a thickness of 140 μm was obtained. The gel fraction of the pressure-sensitive adhesive layer was 28% by mass.

(Example 5)
(5-1) Preparation of acrylic pressure-sensitive adhesive composition (U) 2-ethylhexyl acrylate, methyl methacrylate, N-vinyl-2-pyrrolidone, methacrylic acid are not used, 492.5 parts by mass of n-butyl acrylate and acrylic 7.5 parts by weight of acid is used, and superester E-865NT which is an emulsion-type polymerized rosin ester-based tackifier resin [manufactured by Arakawa Chemical Industries, Ltd .; softening point 160 ° C., solid content 50% by mass] An acrylic pressure-sensitive adhesive composition (U) was obtained in the same manner as in Example 4 except that the amount was reduced from 200 parts by weight to 50 parts by weight. A basis weight of 130 g / m ² and a thickness of 140 μm are the same as in Example 4 except that the acrylic pressure-sensitive adhesive composition (U) is used instead of the acrylic pressure-sensitive adhesive composition (T). No. 2 double-sided pressure-sensitive adhesive tape U-1. The gel fraction of the pressure-sensitive adhesive layer was 26% by mass. The content of the crosslinking agent (solid content) with respect to 100 parts by mass of the acrylic polymer (solid content) was 1.28 parts by mass.

(Example 6)
Same as Example 1 except that a 50 μm thick mesh base material B in which polyester monofilament yarns with a fiber diameter of 25 μm are alternately woven into MD and TD so as to be 132 per inch is used as the base material. Thus, double-sided pressure-sensitive adhesive tape S-5 was obtained. The mesh substrate had a Gurley air permeability of 0.1 sec / 100 ml.

(Example 7)
(7-1) Preparation of acrylic pressure-sensitive adhesive composition (V) In a reaction vessel equipped with a stirrer, a reflux condenser, a nitrogen inlet tube, and a thermometer, 93.4 parts by mass of butyl acrylate, 3 parts by mass of methyl acrylate, acrylic Acetic acid was mixed with 2.3 parts by weight of acid, 1.2 parts by weight of N-isopropylacrylamide, 0.1 part by weight of 2-hydroxyethyl acrylate, and 0.2 part by weight of 2,2′-azobisisobutylnitrile as a polymerization initiator. The resultant was dissolved in 100 parts by mass of ethyl and polymerized at 80 ° C. for 8 hours to obtain an acrylic copolymer solution having a weight average molecular weight of 800,000. 15 parts by mass of rosin ester resin A-100 (Arakawa Chemical Industries, Ltd.) and polymerized rosin ester resin D-135 (Arakawa Chemical Industries, Ltd.) with respect to 100 parts by mass of the acrylic copolymer solid content. Was added and diluted with methyl ethyl ketone to obtain an acrylic pressure-sensitive adhesive composition (V) having a nonvolatile content of 45% by mass.

(7-2) Double-sided adhesive tape V-1
A double-sided pressure-sensitive adhesive tape V-1 was prepared in the same manner as in Example 1 except that the amount of the isocyanate-based crosslinking agent (manufactured by Tosoh Corporation, Coronate L-45E, solid content 45% by mass) was changed to 1.24 parts by mass. Obtained. The gel fraction of the pressure-sensitive adhesive layer was 2% by mass. The content of the crosslinking agent (solid content) with respect to 100 parts by mass of the acrylic polymer (solid content) was 1.61 parts by mass.

Reference example 1
(8-1) Preparation of acrylic pressure-sensitive adhesive composition (W) In a reaction vessel equipped with a stirrer, a reflux condenser, a nitrogen introduction tube, and a thermometer, 76.4 parts by mass of n-butyl acrylate, 2-ethylhexyl acrylate 18 .6 parts by weight, 1.2 parts by weight of acrylic acid, 3.9 parts by weight of vinyl acetate, 0.1 part by weight of 2-hydroxyethyl acrylate, 98 parts by weight of ethyl acetate and stirring, up to 80 ° C. while blowing nitrogen The temperature rose. Thereafter, 2 parts by mass (solid content 5% by mass) of an azobisisobutyronitrile solution previously dissolved in ethyl acetate was added. Then, after holding for 8 hours at 80 ° C. with stirring, the contents were cooled to obtain an acrylic copolymer solution having a weight average molecular weight of 520,000. Polymer rosin ester resin PCJ (manufactured by Harima Chemical Co., Ltd.) 25 parts by mass was mixed with 100 parts by mass of the acrylic copolymer solid content to obtain an acrylic pressure-sensitive adhesive composition (W) having a nonvolatile content of 47% by mass. . The content of the crosslinking agent (solid content) with respect to 100 parts by mass of the acrylic polymer (solid content) was 1.08 parts by mass.

(8-2) Double-sided adhesive tape W-1
A double-sided pressure-sensitive adhesive tape W-1 was prepared in the same manner as in Example 1 except that the amount of the isocyanate-based crosslinking agent (manufactured by Tosoh Corporation, Coronate L-45E, solid content 45% by mass) was 0.90 parts by mass. Obtained. The gel fraction of the pressure-sensitive adhesive layer was 2% by mass.

(Comparative Example 1)
Except having changed the usage-amount of the isocyanate type crosslinking agent (The Tosoh Corporation make, Coronate L-45E, solid content 45 mass%) from 0.52 mass part to 1.1 mass part, it carries out similarly to Example 1. Double-sided pressure-sensitive adhesive tape S-6 was obtained. The gel fraction of the pressure-sensitive adhesive layer was 42% by mass. The content of the crosslinking agent (solid content) with respect to 100 parts by mass of the acrylic polymer (solid content) was 1.61 parts by mass.

(Comparative Example 2)
In Example 1, the total basis weight of the pressure-sensitive adhesive layers provided on both surfaces of the nonwoven fabric was 100 g / m in the same manner as in Example 1 except that the basis weight after drying on the release liner was 50 g / m ^{2. 2.} Double-sided pressure-sensitive adhesive tape S-7 having a pressure-sensitive adhesive layer thickness of 110 μm was prepared.

(Comparative Example 3)
Except having changed the usage-amount of the isocyanate type crosslinking agent (The Tosoh Corporation make, Coronate L-45E, solid content 45 mass%) from 0.52 mass part to 1.9 mass parts, it carries out similarly to Example 1. Double-sided pressure-sensitive adhesive tape S-8 was obtained. The gel fraction of the pressure-sensitive adhesive layer was 52% by mass. The content of the crosslinking agent (solid content) with respect to 100 parts by mass of the acrylic polymer (solid content) was 2.78 parts by mass.

[Create adherend]
100 parts by weight of polyvinyl chloride (degree of polymerization 1400), 34 parts by weight of diisononyl phthalate, 25 parts by weight of calcium carbonate, 3 parts by weight of carbon black, 3 parts by weight of barium-zinc stabilizer and polyvinyl chloride resin compound Was prepared. The obtained polyvinyl chloride resin compound was calendered (processing temperature 170 ° C.) to obtain a polyvinyl chloride sheet having a thickness of 0.4 mm.

[Evaluation method of gel fraction]
The double-sided pressure-sensitive adhesive tapes obtained in the above Examples and Comparative Examples were cut into a size of 40 mm × 50 mm, and then the release liner was peeled off to make a test piece. After measuring the mass of the test piece, the test piece was immersed for 72 hours in a mixed solvent of 70 parts by mass of toluene and 30 parts by mass of methanol adjusted to 23 ° C., and then an ultrasonic device (manufactured by As One Corporation, product Name: US CLEANER US-5R), and vibrated at a frequency of 40 kHz at 23 ° C. for 15 minutes.

  After the vibration, the mass of what remained in the mixed solvent was dried for 1 hour using a dryer (105 ° C.) was measured.

  The gel fraction was calculated based on the mass and the following formula.

Gel fraction (mass%) = {(mass of adhesive layer remaining in mixed solvent) / (mass of adhesive layer before immersion)} × 100
The mass of the pressure-sensitive adhesive layer constituting the pressure-sensitive adhesive tape before immersion refers to a value obtained by subtracting the mass of the air-permeable substrate used for the production from the mass of the double-sided pressure-sensitive adhesive tape. Further, the mass of the remaining pressure-sensitive adhesive layer refers to a value obtained by subtracting the mass of the air-permeable substrate from the mass of the residue after drying.

[Evaluation method of dynamic viscoelasticity]
The pressure-sensitive adhesive layer used in producing the double-sided pressure-sensitive adhesive tape in the above Examples and Comparative Examples was made to have a thickness of 2 mm by laminating a plurality of sheets, and the test piece was cut into a cylindrical shape having a diameter of 8 mm. Using a viscoelasticity testing machine (trade name: ARES-G2 manufactured by TA Instruments Japan Co., Ltd.), a test piece is sandwiched between parallel disks which are measuring parts of the testing machine, and the temperature is 23 ° C., 60 The storage elastic modulus and loss elastic modulus at a frequency of 1 Hz were measured at 100 ° C. and 100 ° C. The ratio of loss elastic modulus to storage elastic modulus (tan δ) was calculated by the following equation. tan δ = loss elastic modulus (Pa) / storage elastic modulus (Pa)

[Evaluation method of initial adhesive strength (T-peel adhesive strength)]
The initial adhesive force was measured according to JIS Z 0237. Specifically, it measured by the following method.

  A double-sided pressure-sensitive adhesive tape from which one release liner was removed was affixed to an adherend (a1-1) and cut into a 15 mm width and a 100 mm length to obtain a test piece. The test piece was left in an atmosphere of 23 ° C. and 50% RH for 1 day. Moreover, what cut the to-be-adhered body (a1-2) in which the double-sided adhesive tape was not affixed into 15 mm width and 100 mm length was left on the same conditions as the said test piece.

  After the leaving, the test piece and the adherend (a1-2) are peeled off and removed from the other release liner of the test piece in an atmosphere of 23 ° C. and 50% RH. a1-2) was affixed, the 2 kg roller was reciprocated once, and left in the same atmosphere for 30 minutes to adhere them.

  One end of the adherend (a1-2) is fixed to the lower chuck of the tensile device of the Tensilon tensile tester, and the adherend (a1-1) is attached to the upper chuck of the tensile device of the Tensilon tensile tester. The adhesive strength (T-peel adhesive strength) was measured by fixing and pulling the upper chuck at a speed of 3 mm / min.

[Method for evaluating adhesive strength after long-term storage (T-peel adhesive strength)]
In the same manner as the evaluation method of the initial adhesive force, a test piece obtained by pasting a double-sided pressure-sensitive adhesive tape from which one of the release liners was removed to the adherend (a1-1) and cutting it to 15 mm width and 100 mm length, and The adherend (a1-2) cut to a width of 15 mm and a length of 100 mm was left for 9 days under wet heat conditions such as 60 ° C. and 80% RH, then taken out in an atmosphere of 23 ° C. and 50% RH, and the test The adherend (a1-2) was affixed to the surface from which the other release liner of the piece was peeled and removed, and the 2 kg roller was reciprocated once and allowed to stand for 30 minutes in the same atmosphere to adhere them.

  One end of the adherend (a1-2) is fixed to the lower chuck of the tensile device of the Tensilon tensile tester, and the adherend (a1-1) is attached to the upper chuck of the tensile device of the Tensilon tensile tester. The adhesive strength (T-peel adhesive strength) was measured by fixing and pulling the upper chuck at a speed of 3 mm / min.

  Moreover, in the case of the measurement of the said adhesive force, how to peel the adhesive tape from a to-be-adhered body (a1-1) or a to-be-adhered body (a1-2) was evaluated on the following references | standards.

[Evaluation criteria]
Cohesive failure: The adherend peeled off due to the cohesive failure of the adhesive layer. Interfacial peeling: In the test piece that was left before leaving wet heat, it peeled off at the interface between the polyvinyl chloride sheet and the double-sided adhesive tape.

(1) Preparation of calibration curve An adhesive prepared by adding 10 parts by mass of diisononyl phthalate used as a plasticizer for a polyvinyl chloride sheet to 100 parts by mass of the solid content of the acrylic adhesive composition (S) was released. A double-sided pressure-sensitive adhesive tape (C1) is formed by applying the adhesive layer to the surface of the liner and drying it, and transferring it to both sides of a 43 μm thick nonwoven fabric A (Nippon Paper Papillia, No. 1215). It was created.

  Next, an acrylic pressure-sensitive adhesive composition (S) containing no plasticizer is applied to the surface of the release liner and dried to form a pressure-sensitive adhesive layer, which is then transferred to both sides of the nonwoven fabric A. A double-sided adhesive tape (C0) was prepared.

  Next, the infrared absorption spectrum of the pressure-sensitive adhesive layer surface of the double-sided pressure-sensitive adhesive tape (C1) was measured by the ATR method to obtain an infrared absorption spectrum (D1).

  Next, the infrared absorption spectrum of the pressure-sensitive adhesive layer surface of the double-sided pressure-sensitive adhesive tape (C0) was measured by the ATR method to obtain an infrared absorption spectrum (D0).

  Next, the infrared absorption spectrum (E1) of the plasticizer was extracted by subtracting the infrared absorption spectrum (D0) from the infrared absorption spectrum (D1) (difference spectrum).

From the infrared absorption spectrum (E1), the height (F1) of the absorption peak at 1285 cm ⁻¹ derived from diisononyl phthalate was measured.

Next, the infrared absorption spectrum of the pressure-sensitive adhesive layer surface of the double-sided pressure-sensitive adhesive tape (C1) is measured by the ATR method to obtain an infrared absorption spectrum (D1). Next, the height (G1) of the absorption peak at 1160 cm ⁻¹ derived from the acrylic polymer was measured from the infrared absorption spectrum (D1).

  Next, an acrylic pressure-sensitive adhesive in which 20 parts by mass of diisononyl phthalate used as a plasticizer for a polyvinyl chloride sheet is added to 100 parts by mass of the solid content of the acrylic pressure-sensitive adhesive composition (S), and 30 parts by mass is added. The acrylic pressure-sensitive adhesive and the acrylic pressure-sensitive adhesive added with 40 parts by mass were prepared, and each pressure-sensitive adhesive was applied to the surface of the release liner and dried to form a pressure-sensitive adhesive layer. 4 types of double-sided pressure-sensitive adhesive tapes were prepared by transferring to both sides.

Next, the release liner of either one of the four types of double-sided pressure-sensitive adhesive tape is removed, and the infrared absorption spectrum of the pressure-sensitive adhesive layer surface is measured by the ATR method. From the four types of infrared absorption spectra, the height of the absorption peak at 1285 cm ⁻¹ derived from diisononyl phthalate and the height of the absorption peak at 1160 cm ⁻¹ derived from the acrylic polymer were measured.

The vertical axis indicates the amount of diisononyl phthalate added to 100 parts by mass of the acrylic copolymer [parts by mass], and the horizontal axis indicates the height (G1) of the absorption peak at 1160 cm ⁻¹ derived from the acrylic polymer. The ratio (F1 / G1) of the absorption peak height (F1) of 1285 cm ⁻¹ derived from diisononyl phthalate (F1 / G1), and the amount of diisononyl phthalate contained in the four types of double-sided adhesive tape and the ratio (F1 / A calibration curve was created by plotting the values corresponding to G1).

  In addition, the said infrared absorption spectrum was measured using the Fourier transform infrared spectrophotometer (JASCO Corporation FT / IR-4100).

  Further, instead of the acrylic pressure-sensitive adhesive composition (S), the acrylic pressure-sensitive adhesive composition (T), the acrylic pressure-sensitive adhesive composition (U), the acrylic pressure-sensitive adhesive composition (V), and the acrylic pressure-sensitive adhesive Calibration curves were prepared in the same manner as described above except that each of the compositions (W) was used.

(2) Measurement of the amount of plasticizer on the surface of the pressure-sensitive adhesive layer After removing the release liner from the surface of the pressure-sensitive adhesive layer corresponding to the pressure-sensitive adhesive layer (b1) of the double-sided pressure-sensitive adhesive tape obtained in Examples and Comparative Examples, the plasticizer Was attached to the above-obtained polyvinyl chloride sheet and left for 9 days in wet heat conditions such as 60 ° C. and 80% RH to obtain a double-sided pressure-sensitive adhesive tape (C2).

Next, the release liner is removed from the surface of the pressure-sensitive adhesive layer corresponding to the pressure-sensitive adhesive layer (b2) of the double-sided pressure-sensitive adhesive tape (C2) after being left, and the infrared absorption spectrum of the surface of the pressure-sensitive adhesive layer (b2) ( D2) was measured by the ATR method, and based on the infrared absorption spectrum (D2), the height of the absorption peak at 1285 cm ⁻¹ derived from diisononyl phthalate (F2) and the absorption at 1160 cm ⁻¹ derived from the acrylic polymer The ratio (F2 / G2) of peak height (G2) was determined.

  Next, F2 / G2 is applied to the horizontal axis of the calibration curve, and the content (H2) of the plasticizer contained in the adhesive layer corresponding to the adhesive layer (b2) of the adhesive tape (C2) [ Parts by mass] were calculated. The content of the plasticizer is the amount of plasticizer transferred from the polyvinyl chloride sheet when the pressure-sensitive adhesive layer corresponding to the pressure-sensitive adhesive layer (b2) excluding the plasticizer is 100 parts by mass. [Mass] is shown.

  Next, the pressure-sensitive adhesive layer (b1) in contact with the polyvinyl chloride sheet is peeled off from the surface of the polyvinyl chloride sheet, and the content of the plasticizer contained in the surface of the pressure-sensitive adhesive layer (b1) (J2) [mass Part] was calculated by the same method as described above.

(3) Evaluation of Uniform Dispersibility of Plasticizer The uniform dispersibility of the plasticizer depends on the difference between the diisononyl phthalate content (H2) obtained by the above method and the diisononyl phthalate content (J2). Based on the following evaluation criteria.

  ◯: The difference between the content (H2) and the content (J2) is within a range of ± 2 parts by mass, and the plasticizer is excellent in uniform dispersibility.

  X: The difference between the content (H2) and the content (J2) is outside the range of ± 2 parts by mass, and the uniform dispersibility of the plasticizer is poor.

[Method of evaluating peel resistance]
One of the tapes obtained by cutting the double-sided pressure-sensitive adhesive tapes obtained in Examples and Comparative Examples to a width of 15 mm on one end of the polyvinyl chloride sheet cut to a width of 50 mm in an environment of 23 ° C. and 50% RH. The pressure-sensitive adhesive surface was attached, and the 2 kg roller was reciprocated once and pressurized. Next, the test piece of the polyvinyl chloride sheet to which the double-sided pressure-sensitive adhesive tape was applied was cut into a length of 100 mm to prepare a test piece having a length of 100 mm and a width of 50 mm. Left for days.

  Next, in a 23 ° C. and 50% RH environment, the polyvinyl chloride sheet was folded in the middle, and the adhesive layer on the other side was attached to the end (center bending attachment).

  Similarly, after leaving the test piece of the polyvinyl chloride sheet with the adhesive tape affixed in an atmosphere of 60 ° C. and 80% RH for 9 days, in a 23 ° C. and 50% RH environment, The sheet was bent into a cylindrical shape, and the pressure-sensitive adhesive layer on the other side was attached to one end of the back surface (spiral winding).

  The test pieces obtained by the center bending and spiral winding were left for 24 hours in a 23 ° C. and 50% RH environment, and their peel resistance was evaluated according to the following criteria.

  A: No peeling occurred in any of the test pieces bonded in the center bending and spiral winding.

  (Circle): All the test pieces paste | laminated by center bending and spiral winding were peeling length of less than 3 mm.

  Δ: Either one of the test pieces bonded to the center bending and spiral winding had a peeling length of 3 mm or more.

  X: All the test pieces pasted by center bending and spiral winding had a peeling length of 3 mm or more.

[Gurley type air permeability of substrate]
The base materials used in the above examples and comparative examples were set by stacking 10 base materials in 23 ° C. and 50% RH, an inner cylinder having a diameter of 28.6 mm and a weight of 567 g dropped, and 100 ml of air was dropped. The transit time was measured. As a measuring instrument, Gurley type air permeability manufactured by Toyo Seiki Seisakusho in accordance with JIS P8117 was used.

Claims (8)

An adhesive tape used for attaching an adherend (a1) containing a plasticizer, having an adhesive layer (b1) on one surface side of a gas-permeable substrate, and an adhesive layer on the other surface side (b2) has, and a range basis weight of total of 125g ^{/ m 2} ~175g ^/ m 2 of the pressure-sensitive adhesive layer (b1) and the pressure-sensitive adhesive layer (b2), and the pressure-sensitive adhesive layer ( The total gel fraction of b1) and the pressure-sensitive adhesive layer (b2) is 2% by mass to 35% by mass, and the pressure-sensitive adhesive layer (b1) and the pressure-sensitive adhesive layer (b2) are derived from a nitrogen-containing vinyl monomer. A pressure-sensitive adhesive tape comprising an adhesive layer containing an acrylic polymer. The pressure-sensitive adhesive tape according to claim 1, wherein the air-permeable substrate is a nonwoven fabric substrate or a porous film substrate having a thickness of 10 to 50 µm. The Gurley type air permeability measured based on JISP8117 of the said test piece is set to 0.35 second / 100ml or less, using what laminated | stacked ten said air-permeable base materials as a test piece, The claim 1 or 2 Adhesive tape. The structure derived from the nitrogen-containing vinyl monomer is a structure derived from N-vinyl-2-pyrrolidone, N-vinylcaprolactam, acryloylmorpholine, dimethylaminoethyl acrylate, N, N-dimethylacrylamide or N-isopropylacrylamide. Item 4. The adhesive tape according to any one of items 1 to 3. The adherend (a1) contains a plasticizer in the range of 15% by mass to 30% by mass with respect to the mass of the adherend (a1), and has a thickness in the range of 0.2 mm to 1 mm. It is a film or a sheet-like material, The adhesive tape of any one of Claims 1-4. The pressure-sensitive adhesive tape according to any one of claims 1 to 5, wherein the plasticizer is a phthalate ester plasticizer. The sheet | seat for wire harness binding which has the structure by which the adhesive tape of any one of Claims 1-6 was stuck to the said to-be-adhered body (a1). An article in which two or more wire harnesses are bound by the wire harness binding sheet according to claim 7.