TWI707936B - Adhesive tape - Google Patents

Abstract

The present invention provides an adhesive tape comprising: a polyvinyl chloride film containing a plasticizer and an adhesive layer arranged on at least one surface of the film. The heating loss of the above adhesive tape is less than 4%, and the holding power is more than 50 minutes.

Description

Adhesive tape

[cross reference]

This application claims priority based on Japanese Patent Application No. 2015-075201 filed on April 1, 2015 and Japanese Patent Application No. 2015-133295 filed on July 2, 2015, and incorporates all the contents of these applications Included in this manual as a reference.

The invention relates to an adhesive tape provided with a polyvinyl chloride (PVC) film.

Adhesive tapes with an adhesive layer arranged on at least one surface of the PVC film (hereinafter also referred to as "PVC adhesive tapes") are widely used in various applications such as electrical insulation, packaging, and protection due to their good workability.

As prior art documents related to PVC adhesive tapes, Japanese Patent Application Publication No. Hei 8-259909 and Japanese Patent Application Publication No. 2009-249510 may be cited.

In Japanese Patent Application Publication No. Hei 8-259909, it is proposed that in order to obtain a PVC adhesive tape with excellent heat degradation resistance and long-term stable adhesion, a polyester plasticizer with a specific viscosity range is formulated in the PVC film In the adhesive layer, a rubber-based adhesive added with a phenolic antioxidant (paragraph 0007, etc.) is used. However, depending on the use of PVC adhesive tape, there is a high level of requirements for heat-resistant deterioration, and the technology described in Japanese Patent Application Publication No. 8-259909 cannot meet the requirements.

The present invention was made in view of the above circumstances, and its object is to provide a PVC adhesive tape with improved heat-resistant deterioration.

The adhesive tape provided by the present invention includes: a polyvinyl chloride film (PVC film) containing a plasticizer, and an adhesive layer disposed on at least one surface of the PVC film. The heating loss of the above adhesive tape is less than 4%. In addition, the adhesive tape preferably has a holding force of 50 minutes or more. In this way, the PVC adhesive tape with less heat loss is excellent in heat deterioration resistance. In addition, the PVC adhesive tape with the above-mentioned holding power has moderate cohesiveness, so it is more rational when it is manufactured or used.

The PVC film constituting the above-mentioned PVC adhesive tape preferably contains a fatty acid metal salt. The adhesive tape of such a structure can easily suppress the heating loss, and can easily obtain good heat resistance deterioration. As the above-mentioned fatty acid metal salt, those containing at least one metal element (excluding Pb) belonging to any one of Group 1, Group 2, Group 12, Group 13 and Group 14 of the periodic table can be preferably used. . Among them, a fatty acid metal salt containing at least one metal element selected from the group consisting of Li, Na, Ca, Mg, Zn, Ba, and Sn is preferred.

The PVC film constituting a preferred aspect of the adhesive tape contains a polyester plasticizer with a molecular weight of 1,000 or more and a carboxylic acid ester with a molecular weight of less than 1,000 as the plasticizer. The PVC adhesive tape with such a structure can easily balance the heat-resistant deterioration and other characteristics (such as initial adhesion or low-temperature characteristics) at a high level.

The PVC film is preferably the weight W _PLH of the polyester plasticizer with a molecular weight of 1000 or more contained in the PVC film and the weight W _PLL of the carboxylic acid ester with a molecular weight of less than 1000 contained in the PVC film. The relationship satisfies the following formula: 1≦(W _PLH /W _PLL )≦50.

Adhesive tapes with such PVC films are easy to balance heat-resistant degradation and other characteristics (such as initial adhesion or low-temperature characteristics) at a higher level.

The PVC film constituting the adhesive tape disclosed here preferably contains an antioxidant. The adhesive tape of such a structure can easily suppress the heating loss, and can easily obtain good heat resistance deterioration.

In addition, according to the present specification, a wire harness is provided, which has a wire harness Any of the adhesive tapes disclosed here are wrapped around it. With such a configuration, it is possible to achieve good heat deterioration resistance in the above-mentioned wire harness.

1, 2‧‧‧PVC adhesive tape

11‧‧‧Support substrate

11A‧‧‧The first side

11B‧‧‧Second side

21、22‧‧‧Adhesive layer

21A‧‧‧Surface (adhesive surface)

Fig. 1 is a cross-sectional view schematically showing the structure of an adhesive tape according to an embodiment.

Fig. 2 is a cross-sectional view schematically showing the structure of an adhesive tape of another embodiment.

Hereinafter, suitable embodiments of the present invention will be described. Conditions other than the matters specifically mentioned in this specification and necessary for the implementation of the invention can be understood by the industry based on the instructions on the implementation of the invention described in this specification and the technical common sense at the time of filing the application. The present invention can be implemented based on the content disclosed in this specification and common technical knowledge in the field.

The adhesive tape disclosed here includes: a PVC film containing a plasticizer, and an adhesive layer disposed on one or both surfaces of the PVC film.

<PVC film>

The above-mentioned PVC film is typically obtained by filming a PVC composition containing a specific component by a known method. Here, the so-called PVC composition refers to a composition in which the main component of the resin component, that is, the component containing more than 50% by weight, is PVC. According to the above-mentioned PVC composition, a PVC film (typically a film containing a soft vinyl chloride resin) exhibiting physical properties suitable as a base material of an adhesive tape can be formed. The proportion of PVC in the resin component contained in the PVC composition is preferably 80% by weight or more, more preferably about 90% by weight or more. It is also possible that the substantial total amount of resin components is PVC.

(PVC)

The PVC constituting the above-mentioned PVC composition can be various polymers with vinyl chloride as the main monomer (the main component in the monomer component, that is, the monomer occupying more than 50% by weight). That is, in the concept of PVC here, in addition to the homopolymer of vinyl chloride, it also includes copolymers of vinyl chloride and various comonomers. As the above-mentioned comonomers, examples include: vinylidene chloride; Alkenes such as olefins and propylenes (preferably olefins with 2 to 4 carbon atoms); acrylic acid, methacrylic acid (hereinafter referred to as "(meth)acrylic acid"), maleic acid, fumaric acid, etc. Carboxyl group-containing monomers or their anhydrides (maleic anhydride, etc.); (meth)acrylates, such as (meth)acrylic acid esters with alkyl alcohols or cycloalkyl alcohols with a carbon number of about 1-10; vinyl acetate, Vinyl ester monomers such as vinyl propionate; styrene, substituted styrene (α-methylstyrene, etc.), vinyl toluene and other styrene monomers; acrylonitrile, etc. As the above-mentioned copolymer, it is preferable that the copolymerization ratio of vinyl chloride is 70 weight% or more (more preferably 90 weight% or more). PVC is obtained by polymerizing such monomers by an appropriate method (typically a suspension polymerization method).

Although it is not particularly limited, the average degree of polymerization of PVC contained in the PVC composition can be, for example, about 800 to 1800. Considering the balance between processability (formability) and strength, etc., it is preferably a PVC composition whose average degree of polymerization is in the range of about 1000 to 1600 (for example, about 1200 to 1500).

(Plasticizer)

As the plasticizer, various materials known to exhibit the plasticizing effect of PVC can be used without particular limitation. As examples of the above-mentioned plasticizers, parabens (diol benzoate etc.), phthalates, and terephthalates (di(2-ethylhexyl terephthalate) ) Ester, etc.), trimellitate, pyromellitic acid ester and other aromatic carboxylic acid esters; adipate, sebacate, azelate, maleate, citrate (acetyl Aliphatic carboxylic acid esters such as tributyl citrate, etc.; polyesters of polycarboxylic acids and polyols; in addition, polyether polyesters, epoxy polyesters (epoxidized soybean oil or epoxidized linseed oil) Such as epoxidized vegetable oil, epoxidized fatty acid alkyl ester, etc.), phosphoric acid ester (tricresyl phosphate), etc., but not limited to these. The plasticizer can be used alone or in appropriate combination of two or more.

As the above-mentioned phthalates (phthalate-based plasticizers), for example, phthalic acid and a carbon number of 4 to 16 (preferably 6 to 14, typically 8 to 13) can be used Suitable examples of diesters of alkyl alcohol include di-n-octyl phthalate, di(2-ethylhexyl) phthalate, diisononyl phthalate, and phthalic acid Diisodecyl ester and so on.

As the above-mentioned trimellitate (trimellitic acid ester-based plasticizer), for example, a triester of trimellitic acid and an alkyl alcohol having 6 to 14 carbon atoms (typically 8 to 12) can be used. Examples include: tri-n-octyl trimellitate, tris(2-ethylhexyl) trimellitate, triisononyl trimellitate, tri-n-decyl trimellitate, trimellitic acid Triisodecyl ester and so on.

As the aforementioned pyromellitic acid ester (pyromellitic acid ester-based plasticizer), for example, a tetraester of pyromellitic acid and an alkyl alcohol having 6 to 14 carbon atoms (typically 8 to 12) can be used. Suitable examples include tetra-n-octyl pyromellitic acid, tetra-(2-ethylhexyl) pyromellitic acid, and tetra-n-decyl pyromellitic acid.

As the above-mentioned adipate (adipate-based plasticizer), for example, two of adipic acid and an alkyl alcohol having 4 to 16 carbon atoms (preferably 6 to 14 and typically 8 to 13) can be used Suitable examples of the ester include di-n-octyl adipate, di(2-ethylhexyl) adipate, diisononyl adipate, and the like.

As the polyester (polyester plasticizer), for example, succinic acid, adipic acid, suberic acid, azelaic acid, sebacic acid, citric acid, phthalic acid, isophthalic acid, p- Polycarboxylic acids such as phthalic acid and trimellitic acid and (poly)ethylene glycol ("(poly)ethylene glycol" herein collectively refer to the meaning of ethylene glycol and polyethylene glycol. The following is the same ), (poly) propylene glycol, (poly) butylene glycol, (poly) hexanediol, (poly) neopentyl glycol, polyvinyl alcohol and other polyols derived from polyester compounds. The above-mentioned polycarboxylic acid is preferably an aliphatic dicarboxylic acid having 4 to 12 carbon atoms (typically 6 to 10), and suitable examples include adipic acid and sebacic acid. Especially in terms of versatility and price, adipic acid is more desirable. The above-mentioned polyol is preferably an aliphatic diol having 2 to 10 carbon atoms, and suitable examples include ethylene glycol and butanediol (for example, 1,3-butanediol and 1,4-butanediol) Wait.

The amount of plasticizer in the PVC film is not particularly limited. The blending amount of the plasticizer is appropriately set, for example, in such a way that the desired plasticizing effect can be obtained and the heating loss is sufficiently suppressed. The content of the plasticizer is usually set to 1% by weight or more of the PVC film (typically 5% by weight or more, for example, 10% by weight or more). From the viewpoint of obtaining a better plasticizing effect, Preferably it is 15 weight% or more. The content of the plasticizer may be 20% by weight or more, and may be further 25% by weight or more (for example, 30% by weight or more). In addition, the content of the plasticizer can be, for example, 60% by weight or less of the PVC film. From the viewpoint of reducing the heating loss, it is usually preferably 50% by weight or less, and more preferably 40% by weight or less. The technology disclosed here can also be implemented preferably in a state where the content of the plasticizer is less than 35% by weight of the PVC film (typically less than 35% by weight, for example, less than 33% by weight).

Although it is not particularly limited, it is usually appropriate to set the blending amount of the plasticizer relative to 100 parts by weight of PVC to 10 to 75 parts by weight. From the viewpoint of taking into account the heat-resistant degradation and other characteristics at a high level, the blending amount of the plasticizer relative to 100 parts by weight of PVC is preferably 20-60 parts by weight, more preferably 30-50 parts by weight .

In a preferred aspect of the technology disclosed herein, the above-mentioned PVC film combination contains a polyester plasticizer with a molecular weight of 1,000 or more and a carboxylic acid ester with a molecular weight of less than 1,000 as the plasticizer. According to this aspect, it is easy to obtain an adhesive tape that balances heat-resistant deterioration and other characteristics at a higher level.

Generally speaking, polyester plasticizers with a molecular weight of 1000 or more are difficult to volatilize, and it is easy to maintain the plasticizing effect even after the PVC adhesive tape is kept at high temperature for a long time. On the other hand, polyester plasticizers with a molecular weight of 1,000 or more reduce the plasticizing effect at low temperatures due to the viscosity of the plasticizer itself. Therefore, the flexibility required for PVC adhesive tapes tends to be insufficient. On the other hand, carboxylic acid esters with a molecular weight of less than 1000 exhibit excellent flexibility even at low temperatures, but are easy to volatilize at high temperatures and disappear from the PVC film, thereby easily causing the heat resistance of the adhesive tape to deteriorate.

The inventors found that by using a combination of a polyester plasticizer (PLH) with a molecular weight of 1,000 or more and a carboxylic acid ester (PLL) with a molecular weight of less than 1,000, the volatilization of PLL at high temperatures is suppressed, thereby achieving heat resistance The deterioration is improved, and the PVC adhesive tape maintains suitable flexibility in a wide temperature range from high temperature to low temperature. When implementing the technology disclosed here, there is no need to clarify the reason for the above effect, but it is believed that the intermolecular interaction between PLL and PLH It reduces the volatility of PLL. In addition, the inventors found that compared with the case of using a PVC film containing PLL as a plasticizer alone, in an adhesive tape using a PVC film containing PLL and PLH in combination, the adhesive force changes over time (typically For the decrease in adhesion) is suppressed. It is believed that the reason is that one of the reasons for the change in the above-mentioned adhesive force over time is that when PLL is transferred to the adhesive layer, PLH is used in combination with PLL, which may be due to the molecular interaction between PLL and PLH and the interaction between PLH and PLH. The interaction of PVC inhibits the transfer of PLL to the adhesive layer, thereby suppressing the change of adhesive force with time. In this way, by using PLH and PLL in combination, it is possible to achieve a higher level of compatibility with thermal degradation and other characteristics compared to a configuration using PLH or PLL alone.

Furthermore, in this specification, the "molecular weight" of the plasticizer refers to the weight average molecular weight grasped based on the following "(2-2) Molecular Weight Analysis by GPC".

As the carboxylic acid ester (PLL) with a molecular weight of less than 1,000, one kind can be used alone or in combination of two or more of the above-mentioned aromatic carboxylic acid ester, aliphatic carboxylic acid ester and polyester whose molecular weight is less than 1,000. For example, phthalates (di-n-octyl phthalate, bis(2-ethylhexyl) phthalate, diisononyl phthalate, diisodecyl phthalate) can be used Esters, etc.), adipates (di-n-octyl adipate, di(2-ethylhexyl) adipate, diisononyl adipate, etc.), trimellitate (trimellitic acid Tri-n-octyl ester, trimellitic acid tris (2-ethylhexyl) ester, etc.), pyromellitic acid ester (tetra-n-octyl pyromellitic acid, pyromellitic acid tetra-(2-ethylhexyl) ester , Pyromellitic acid tetra-n-decyl ester, etc.), citrate, sebacate, azelate, maleate, benzoate, etc.

As the PLL, aromatic carboxylic acid esters can be preferably used. Among them, preferred are ester compounds derived from aromatic carboxylic acids having trifunctional or higher functions (typically trifunctional or tetrafunctional), and specific examples include trimellitic acid esters and pyromellitic acid esters. This kind of PLL easily exerts the effect brought about by the above-mentioned intermolecular interaction, and the compatibility with PVC is also good. Moreover, compared with the ester compound derived from a monofunctional or difunctional aromatic carboxylic acid, there exists a tendency for volatility to be lower, and it is also preferable in this respect.

The molecular weight of PLL is typically 250 or more, and from the viewpoint of suppressing volatilization and easily achieving the desired heating loss, it is preferably 400 or more, more preferably 500 or more. The technology disclosed herein can be implemented preferably using a PLL with a molecular weight of 600 or more (more preferably 650 or more, for example, 700 or more). The upper limit of the molecular weight of PLL is not particularly limited as long as it is less than 1,000. From the viewpoint of handling properties and the like, it is generally preferable to use a PLL with a molecular weight of 950 or less (for example, 900 or less).

The carbon number of the ester residue in PLL is preferably 6 or more, more preferably 8 or more. Such a PLL easily exerts the effects brought about by the aforementioned intermolecular interaction. In addition, the increase in molecular weight tends to decrease volatility, which is also preferable in this respect. Furthermore, by making the molecular chain longer, the flexibility is increased, and it is easy to become a liquid form at room temperature, thereby improving the handling properties. The upper limit of the carbon number of the ester residue is not particularly limited. From the viewpoint of handling properties or compatibility with PVC, it is usually 16 or less, preferably 14 or less, and more preferably 12 or less (for example, 10 or less) .

Although there is no particular limitation, the blending amount of PLL relative to 100 parts by weight of PVC (in the case of using more than two types, the total amount) is usually less than 75 parts by weight, preferably less than 60 parts by weight. More preferably, it is less than 50 parts by weight. From the viewpoint of easy reduction of heating loss, it is advantageous to set the blending amount of PLL to 100 parts by weight of PVC to be 30 parts by weight or less, preferably 20 parts by weight or less, and more preferably 15 parts by weight or less. The technology disclosed here can also be implemented preferably with respect to a state where the blending amount of PLL of 100 parts by weight of PVC is 10 parts by weight or less. The lower limit of the PLL blending amount can be set in such a way that the desired flexibility can be obtained, and it is generally appropriate to set it to be 1 part by weight or more (preferably 3 parts by weight or more, for example, 5 parts by weight or more) relative to 100 parts by weight of PVC.

As the polyester plasticizer (PLH) with a molecular weight of 1,000 or more, one type may be used alone or in combination of two or more of the polyester plasticizers with a molecular weight of 1,000 or more. From the viewpoint of plasticizing effect or softness at low temperature, a polyester of aliphatic dicarboxylic acid and polyol having 4 to 12 carbon atoms (typically 6 to 10) is preferred. Among them, it is better to Adipic acid polyester plasticizer obtained from dicarboxylic acid and aliphatic diols such as neopentyl glycol, propylene glycol and ethylene glycol as the main component. The reason is that this adipic acid-based polyester plasticizer is rich in intermolecular interactions with PLL and PVC, thereby exerting the effect of suppressing the volatilization of PLL and further suppressing the volatility of PLH itself.

Commercial products that can be used as PLH in the technology disclosed here can be specifically listed: DIC Co., Ltd.’s trade names "W-230H", "W-1020EL", "W-1410EL", "W-2050", "W-2300", "W-2310", "W-2360", "W-360ELS", "W-4010", etc.; ADEKA Co., Ltd. trade names "P-300", "PN-250", "PN-400", "PN-650", "PN-1030", "PN-1430", etc.; Kao Corporation's product name "HA-5", etc.

The molecular weight of PLH is not particularly limited as long as it is 1000 or more. From the viewpoint of easily achieving the desired heating loss, it is generally advantageous to use PLH with a molecular weight of 2000 or more (preferably 2500 or more, for example, 3000 or more). The technology disclosed here can be implemented preferably using PLH with a molecular weight of 4000 or more (for example, 5000 or more). The upper limit of the molecular weight of PLH is not particularly limited, and it is generally appropriate to set it to less than 100,000. From the viewpoint of better exerting the plasticizing effect of PVC and easily achieving the flexibility required by the PVC adhesive tape, the molecular weight of PLH is preferably less than 50,000, more preferably less than 25,000, and even more preferably less than 10,000 (For example, 7000 or less). The technique disclosed here can also be suitably implemented in the form of containing PLH with a molecular weight of 4500 or less (furthermore, 3500 or less, for example, less than 3000).

Although not particularly limited, the blending amount of PLH relative to 100 parts by weight of PVC (in the case of using two or more types, the total amount of these) is usually set to less than 75 parts by weight, preferably less than 60 parts by weight, more preferably less than 50 parts by weight. From the viewpoint of easy reduction of heating loss, the blending amount of PLH relative to 100 parts by weight of PVC is preferably 40 parts by weight or less, and more preferably 30 parts by weight or less. The lower limit of the blending amount of PLH can be set in such a way that the desired flexibility can be obtained. It is usually set to 5 relative to 100 parts by weight of PVC. Part by weight or more (preferably 8 parts by weight or more, for example, 10 parts by weight or more) is appropriate. The technology disclosed here can also be preferably implemented with a blending amount of 15 parts by weight or more of PLH relative to 100 parts by weight of PVC, and further more than 20 parts by weight.

The ratio of the deployment amount of PLH to the deployment amount of PLL is not particularly limited. For example, the ratio (W _PLH /W _PLL ) of the weight of PLH contained in the PVC film (W _PLH ) to the weight of _PLL (W _PLL ) (W _PLH /W _PLL ) can be set to about 0.1 to 500. From the viewpoint of reducing heating loss, it is generally advantageous to set W _PLH /W _PLL to 0.5-100, and preferably 1-50. In terms of a higher level of compatibility with heat deterioration resistance and other characteristics (suppression of adhesion over time, flexibility in a wider temperature range, etc.), in a better aspect, W _PLH can be used /W _{PLL is} set to 1 to 25, more preferably 1 to 15 (for example, 1 to 10), and even more preferably to 1 to 7 (typically 1 or more and less than 5, for example, 1 to 4.5).

(Fatty acid metal salt)

The PVC film in the technology disclosed here preferably contains fatty acid metal salt in addition to PVC and plasticizer. PVC film has the following situations: during the processing of the PVC film or PVC adhesive tape or in the use environment of the adhesive tape, the PVC contained in the above-mentioned PVC film is subjected to physical energy such as heat, ultraviolet rays or shearing force, etc. , Discoloration occurs due to chemical reactions caused by this, or physical, mechanical or electrical properties are impaired. By making the PVC film contain fatty acid metal salt, the fatty acid metal salt can function as a stabilizer to prevent or inhibit the above-mentioned chemical reaction. In addition, preventing or suppressing the above-mentioned chemical reaction (typically the detachment of hydrogen chloride) helps to suppress the heating loss, and thus can make a beneficial contribution to the improvement of the heat-resistant deterioration of the PVC adhesive tape.

As the fatty acid metal salt, one compound can be used alone or in combination of two or more compounds that can function as a stabilizer of the PVC film. For example, the fatty acid constituting the fatty acid gold salt may be preferably selected from saturated or unsaturated fatty acids (which may be lauric acid, ricinoleic acid, stearic acid, etc.) with a carbon number of about 10-20 (typically 12-18). Hydroxy fatty acids). From the viewpoint of the formability or processability of PVC film, stearic acid can be preferably used Metal salt. In addition, from the viewpoints of suppression of changes over time of the PVC film or PVC adhesive tape, and flexibility at low temperatures, metal lauric acid salts can be preferably used. In a preferred aspect, metal stearate and metal laurate can be used in combination. In this case, the ratio of the usage amount of lauric acid metal salt to the usage amount of stearate metal salt is not particularly limited, for example, it can be set to 0.1~10 on a weight basis, usually 0.2~5 (for example 0.5~2) is more appropriate.

As the metal constituting the fatty acid metal salt, a metal other than lead (non-lead metal) can be preferably used in consideration of the increasing awareness of environmental hygiene in recent years. According to the technology disclosed here, it is possible to realize a PVC adhesive tape that exhibits good heat-resistant deterioration even in such a state where no lead-containing stabilizer is used. As the above metal, for example, a metal element belonging to any one of Group 1, Group 2, Group 12, Group 13 and Group 14 (except Pb) of the periodic table can be selected. As a suitable example, Li , Na, Ca, Mg, Zn, Ba and Sn. As the aforementioned fatty acid metal salt, a Ca salt or a Ba salt can be preferably used from the viewpoints of cost or availability. In addition, from the viewpoint of the formability and processability of the PVC film, Zn salt can be preferably used. In a preferred aspect, Ca salt and Zn salt can be used in combination. In this case, the ratio of the usage amount of the Zn salt to the usage amount of the Ca salt is not particularly limited. For example, it can be set to 0.1~10 on a weight basis, usually 0.2~5 (for example, 0.5~2). appropriate. The technique disclosed here can be preferably implemented in a state where Ca stearate and Zn lauric acid are contained in the above weight ratio, or a state where Zn stearate and Ca lauric acid are contained in the above weight ratio. Furthermore, in applications that allow the use of fatty acid Pb salts, the PVC film may also contain fatty acid Pb salts.

The amount of fatty acid metal salt used is not particularly limited. The amount of fatty acid metal salt used (in the case of using two or more types, the total amount), for example, can be 0.01 parts by weight or more relative to 100 parts by weight of PVC. From the viewpoint of obtaining higher effects, it is preferable It is 0.05 weight part or more, More preferably, it is 0.1 weight part or more (for example, 0.12 weight part or more). The upper limit of the amount of fatty acid metal salt used is not particularly limited, usually relative to 100 weight The amount of PVC is preferably 5 parts by weight or less. From the viewpoint of flexibility at low temperatures, it is preferably 3 parts by weight or less, and more preferably 1 part by weight or less (for example, 0.5 parts by weight or less). In one aspect, the usage amount of the fatty acid metal salt relative to 100 parts by weight of PVC can also be set to 0.3 parts by weight or less (for example, less than 0.2 parts by weight).

(Antioxidants)

In addition to PVC and plasticizer, the PVC film in the technology disclosed here may also contain antioxidants. By making the PVC film contain an antioxidant, there is a tendency that heating loss is suppressed. Therefore, it is possible to realize a PVC adhesive tape with better resistance to heat deterioration. In addition, by using the heating loss suppression effect obtained by the antioxidant, the design freedom of the composition (type or amount of plasticizer) of the PVC film can be increased, thereby achieving a higher level of compatibility between heat resistance and other properties The adhesive tape.

As the antioxidant, a known material capable of exerting an antioxidant function can be used without particular limitation. Examples of antioxidants include phenol-based antioxidants, phosphorus-based antioxidants, sulfur-based antioxidants, and amine-based antioxidants. Antioxidant can be used individually by 1 type or in combination of 2 or more types.

Suitable examples of antioxidants include phenol-based antioxidants such as hindered phenol-based antioxidants. Examples of hindered phenol-based antioxidants include: pentaerythritol tetra[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate] (trade name "Irganox 1010", Ciba Corporation Manufacture), 3-(3,5-di-tert-butyl-4-hydroxyphenyl) stearyl propionate (trade name "Irganox 1076", manufactured by Ciba Corporation), 4,6-di (Dodecylthiomethyl)-o-cresol (trade name "Irganox 1726", manufactured by Ciba Corporation), triethylene glycol bis[3-(3-tertiarybutyl-5-methyl-4) -Hydroxyphenyl) propionate] (trade name "Irganox 245", manufactured by Ciba Corporation), bis(2,2,6,6-tetramethyl-4-piperidyl) sebacate (commodity The name "TINUVIN 770", manufactured by Ciba Corporation), the condensation polymer of dimethyl succinate and 4-hydroxy-2,2,6,6-tetramethyl-1-piperidine ethanol (dimethyl succinate- 1-(2-hydroxyethyl)-4-hydroxy-2,2,6,6-tetramethylpiperidine polycondensate) (trade name "TINUVIN 622", manufactured by Ciba Corporation), etc. its Among them, pentaerythritol tetrakis[3-(3,5-di-tert-butyl-4-hydroxyphenyl) propionate] (trade name "Irganox 1010", manufactured by Japan Ciba Corporation), triethylene two Alcohol bis[3-(3-tert-butyl-5-methyl-4-hydroxyphenyl)propionate] (trade name "Irganox 245", manufactured by Ciba Corporation) and the like.

The amount of antioxidant used (when two or more types are used, the total amount thereof) is not particularly limited, and for example, it can be 0.001 parts by weight or more with respect to 100 parts by weight of PVC. From the viewpoint of obtaining a higher effect, it is generally appropriate to set the amount of antioxidant to 100 parts by weight of PVC to be 0.01 parts by weight or more, preferably 0.05 parts by weight or more, and more preferably 0.1 parts by weight More than. In a preferred aspect, the amount of antioxidant used relative to 100 parts by weight of PVC can be set to 0.5 parts by weight or more, 1 part by weight or more, and further 2 parts by weight or more (for example, 3 parts by weight). Parts by weight or more). The upper limit of the amount of antioxidant used is not particularly limited, but it is usually 10 parts by weight or less (for example, 5 parts by weight or less) relative to 100 parts by weight of PVC.

(Elastomer)

In addition to PVC and plasticizers, the PVC film in the technology disclosed herein may also contain elastomers. By making the PVC film contain elastomers, the low-temperature properties of the PVC adhesive tape (such as flexibility at low temperatures) can be improved, and the mechanical strength of the PVC film can be improved (for example, even if the PVC film is further thinned, it can be achieved. Expected mechanical strength) and other effects. In addition, by including elastomer in the PVC film, the heating loss of the PVC adhesive tape can be reduced.

As the elastomer, various known polymer materials can be used. As non-limiting examples of such elastomers, chlorinated polyethylene (CPE), ethylene-vinyl acetate copolymer, vinyl chloride-vinyl acetate copolymer (for example, vinyl acetate content of about 10% by weight or more, Typically about 10-25% by weight of vinyl chloride-vinyl acetate copolymer), (meth)acrylate-butadiene-styrene copolymer (for example, methyl methacrylate-butadiene-styrene Copolymer), acrylonitrile-butadiene-styrene copolymer, acrylonitrile-butadiene copolymer, styrene-butadiene copolymer (typically styrene-butadiene block copolymer, such as Styrene content is about 35% by weight or less, typically about 10 to 35% by weight styrene-butadiene block copolymer), styrene-butadiene-styrene block copolymer, chlorosulfonated poly Ethylene (CSM), polyester-based thermoplastic elastomers, thermoplastic polyurethanes, other synthetic rubbers (isoprene rubber, butadiene rubber, etc.), these compounds or modified products, etc. Elastomers can be used alone or in combination of two or more.

In the technology disclosed here, as the elastomer contained in the PVC film, it is preferable to select a material with good compatibility with PVC. Thereby, the low-temperature characteristics of the PVC film and the PVC adhesive tape using the PVC film can be effectively improved. From the viewpoint of the appearance quality of the PVC adhesive tape, etc., the above-mentioned elastomer is preferably used with a composition (content) within a range that achieves a good compatibility state in the PVC film. The aforementioned compatibility state can be grasped, for example, by observing the presence or absence of white turbidity on the PVC film directly or in a state of stretching (for example, extending to about 2 times in the traveling direction).

As a non-limiting example of elastomers that can be preferably used in the technology disclosed herein, chlorinated polyethylene (for example, the chlorine content is about 25-50% by weight, typically about 30-45% by weight, more Preferably about 35~45% by weight of chlorinated polyethylene), (meth)acrylate-butadiene-styrene copolymer, acrylonitrile-butadiene copolymer (for example, the content of acrylonitrile is about 15-50% by weight) %, typically about 25 to 45% by weight, preferably about 30 to 40% by weight of acrylonitrile-butadiene copolymer), ethylene-vinyl acetate copolymer (for example, the content of vinyl acetate is about 30 to 75 % By weight, typically about 40 to 70% by weight, preferably about 50 to 65% by weight of ethylene-vinyl acetate copolymer) and the like.

The content of the elastomer is not particularly limited. The content of the elastomer relative to 100 parts by weight of PVC can be, for example, 0.5 parts by weight or more, usually 1 part by weight or more is appropriate, and from the viewpoint of obtaining higher effects, it is preferably 2 parts by weight or more. In addition, from the viewpoint of easily achieving a balance between the effect of using the elastomer and other characteristics, the content of the elastomer relative to 100 parts by weight of PVC is usually 40 parts by weight or less, preferably 30 parts by weight or less. In a preferred aspect, the content of the elastomer relative to 100 parts by weight of PVC can be set to 3-20 parts by weight (for example, 5-15 parts by weight).

The PVC film in the technology disclosed herein may further contain well-known additives that can be used in PVC films (especially PVC films for PVC adhesive tapes) as needed within a range that does not significantly hinder the effects of the present invention. Examples of such additives include: colorants such as pigments or dyes, stabilizers other than fatty acid metal salts (for example, organotin compounds such as dioctyltin laurate), and stabilization aids (for example, trialkyl phosphite) Inorganic compounds such as phosphites, hydrotalcite or zeolite), light stabilizers, ultraviolet absorbers, modifiers, flame retardants, antistatic agents, antifungal agents, lubricants, etc.

The PVC film of such a composition is typically obtained by forming a PVC composition having a corresponding composition into a film shape using a method known in the art of thermoplastic resin film. As such a known molding method, for example, a melt extrusion molding method (inflation method, T die method, etc.), melt casting method, calendering method, etc. can be used. The technology disclosed here can be preferably implemented even in the aspect of the above-mentioned PVC film that uses treatments that have not implemented the addition of a crosslinking agent or irradiation of active energy rays to deliberately improve the crosslinkability of the PVC film as a whole. . According to this PVC film, there is a tendency to obtain a PVC adhesive tape with higher flexibility.

As an example, the outline of a typical film production procedure when the calendering method is used is shown below.

(1) Measurement: Measure PVC, plasticizer and other materials as needed according to the target composition.

(2) Mixing: Stir and mix the measured materials to prepare a uniform mixture (typically a powdery mixture, that is, mixed powder).

(3) Kneading: The mixture prepared in (2) above is heated to melt, and kneading is performed with two or three kneading rolls (typically metal rolls). The temperature of the kneading roll is suitably set to, for example, 100°C to 250°C (preferably 150°C to 200°C).

(4) Calendering: Put the kneaded product obtained in (3) above into a calendering machine to form a PVC film with any thickness.

In the adhesive tape disclosed here, the above-mentioned PVC film may constitute a single layer containing the PVC film or A multi-layer supporting substrate can also constitute a supporting substrate containing other layers in addition to the PVC film. In a preferred aspect, the above-mentioned other layer may be an auxiliary layer such as a printing layer, a peeling treatment layer, a primer layer and the like provided on the surface of the PVC film. Alternatively, the above-mentioned PVC film may constitute a supporting base material in which the PVC film and a resin film other than the PVC film are laminated. As a preferred aspect, a structure in which an adhesive layer is arranged on one side of a support substrate including a single-layer PVC film can be cited.

The thickness of the supporting substrate is not particularly limited. The thickness of the supporting substrate (for example, a supporting substrate including a single-layer PVC film) is typically 500 μm or less, usually 300 μm or less. From the viewpoint of the rationality of the PVC adhesive tape, it is preferably 200 μm or less, more preferably 150 μm or less (for example, 120 μm or less). In addition, the thickness of the support substrate is typically 10 μm or more, and usually 25 μm or more. From the viewpoint of strength and handling properties, it is preferably 50 μm or more, and more preferably 75 μm or more. The thickness of the above-mentioned support base material can be preferably applied to, for example, the protection of wires, piping, etc., or the adhesive tape used in the coating of corrugate tubes that surround and protect the surrounding wires, etc., and for electrical insulation. .

The surface of the adhesive layer is arranged on the supporting substrate, and corona discharge treatment, plasma treatment, ultraviolet irradiation treatment, acid treatment, alkali treatment, coating of primer (primer), antistatic treatment, etc. can also be carried out if necessary Previously known surface treatment. Such surface treatment can be a treatment to improve the adhesion between the substrate and the adhesive layer, in other words, to improve the grip of the adhesive layer on the substrate. The composition of the primer is not particularly limited, and can be appropriately selected from known ones. The thickness of the undercoat layer is not particularly limited, but it is usually preferably 0.01 μm or more and 1 μm or less, and more preferably 0.1 μm or more and 1 μm or less.

In a PVC adhesive tape with an adhesive layer on only one surface of the support substrate, the surface (back) on the side where the adhesive layer is not provided can also be peeled off or antistatically treated as required. . For example, by providing a long-chain alkyl-based, silicone-based peeling treatment layer on the back of the substrate, the unwinding force of the PVC adhesive tape wound in a roll shape can be reduced. In addition, it is also possible to improve printability, reduce light reflectivity, and overlap For the purpose of improving adhesion, etc., treatments such as corona discharge treatment, plasma treatment, ultraviolet irradiation treatment, acid treatment, and alkali treatment are performed on the above-mentioned back surface.

<Adhesive layer>

The adhesive layer in the technology disclosed here is typically a layer containing a material (adhesive) with the following properties: it presents a soft solid (viscoelastic body) state in a temperature region near room temperature, and simply presses Connect with the adherend. The so-called adhesive here is as defined in "CADahlquist, "Adhesion: Fundamental and Practice", McLaren & Sons, (1966), P.143", and generally can have a complex tensile modulus E*(1Hz) Materials with properties of <10 ⁷ dyne/cm ² (typically materials with the above properties at 25°C).

The adhesive layer in the technology disclosed herein can be composed of a water-dispersible adhesive composition, a water-soluble adhesive composition, a solvent-based adhesive composition, a hot-melt adhesive composition, and an active energy ray hardening adhesive. Adhesive layer formed by various forms of adhesive composition such as composition. Here, "active energy rays" refer to energy rays that can cause chemical reactions such as polymerization reactions, cross-linking reactions, and decomposition of initiators, and include light such as ultraviolet rays, visible rays, infrared rays, or α The concepts of radiation, beta rays, gamma rays, electron beams, neutron rays, and X-ray radiation. In terms of inhibiting the transfer of the plasticizer in the PVC film to the adhesive layer and easily inhibiting the change of the adhesive force with time, the adhesive layer formed of a water-dispersed adhesive composition is preferred.

The type of the adhesive constituting the above-mentioned adhesive layer is not particularly limited. The above-mentioned adhesive may be a rubber polymer, acrylic polymer, polyester polymer, urethane polymer, polyether polymer, polysiloxane polymer, which is well-known in the adhesive field. , One or two or more of various rubber-like polymers such as polyamide-based polymers and fluorine-based polymers as the base polymer (the main component in the polymer component). Here, the rubber-based adhesive means an adhesive that contains a rubber-based polymer as a base polymer. The same applies to acrylic adhesives and other adhesives. Also, the so-called acrylic polymer refers to Polymers containing monomer units derived from monomers (acrylic monomers) having at least one (meth)acrylic acid group in a molecule in the polymer structure, typically referring to a ratio of more than 50% by weight A polymer of monomer units derived from acrylic monomers. In addition, the above-mentioned (meth)acryloyl group collectively refers to the meaning of an acrylic group and a methacryloyl group.

As the adhesive layer of the PVC adhesive tape disclosed here, an adhesive layer (rubber-based adhesive layer) with a rubber-based adhesive as the main component can be preferably used. The rubber-based adhesive may be one containing one or two or more rubber-based polymers selected from natural rubber and synthetic rubber. In addition, in this specification, the term "principal component" means a component containing more than 50% by weight when there is no special description. As the rubber-based polymer, either natural rubber or synthetic rubber can be used. As the natural rubber, known materials that can be used in the adhesive composition can be used without particular limitation. The so-called natural rubber here is not limited to unmodified natural rubber, but includes, for example, the concept of modified natural rubber modified by acrylate or the like. Unmodified natural rubber and modified natural rubber can also be used together. As the synthetic rubber, known materials that can be used in the adhesive composition can be used without particular limitation. Suitable examples include styrene-butadiene rubber (SBR), styrene-isoprene rubber, and chloroprene rubber. These synthetic rubbers can be unmodified or modified (for example, carboxyl modification). The rubber-based polymer can be used alone or in combination of two or more.

A preferred aspect of the PVC adhesive tape has a rubber-based adhesive layer formed of a water-dispersible rubber-based adhesive composition. The water-dispersible rubber-based adhesive composition is formulated in rubber latex with an adhesion-imparting resin and Made from other additives. The above-mentioned rubber-based latex may be obtained by dispersing various known rubber-based polymers in water. Either natural rubber latex and synthetic rubber latex can be used. As the natural rubber latex, known materials that can be used in the adhesive composition can be used without particular limitation. The so-called natural rubber latex here is not limited to unmodified natural rubber latex, and includes, for example, the concept of modified natural rubber latex modified by acrylate or the like. Unmodified natural rubber latex Rubber and modified natural rubber latex are used together. As the synthetic rubber latex, known materials that can be used in the adhesive composition can be used without particular limitation. Suitable examples include styrene-butadiene rubber latex (SBR latex), styrene-isoprene rubber latex, and chloroprene rubber latex. The synthetic rubber contained in the synthetic rubber latex may be unmodified or modified (for example, carboxyl group modification). The rubber latex can be used alone or in combination of two or more.

A preferred aspect of the rubber-based adhesive composition (for example, a water-dispersed rubber-based adhesive composition) contains both natural rubber and synthetic rubber as the rubber-based polymer. According to this adhesive composition, a PVC adhesive tape showing good adhesive properties can be formed. For example, it is possible to form a PVC adhesive tape that exhibits adhesive properties suitable for the protection or bundling of electric wires, piping, etc., as described above, for the coating of corrugated pipes, and electrical insulation. The weight ratio of natural rubber to synthetic rubber (natural rubber: synthetic rubber) is preferably in the range of about 10:90 to 90:10, more preferably in the range of about 20:80 to 80:20, and even more preferably about The range of 30:70~70:30. As the above synthetic rubber, SBR can be preferably used.

The adhesive layer (typically a rubber-based adhesive layer) in the technology disclosed here may contain an adhesion-imparting resin in addition to the base polymer as described above. As the adhesion-imparting resin, an appropriate one can be selected and used from various known adhesion-imparting resins. For example, one or two or more of various adhesion-imparting resins selected from rosin-based resins, petroleum resins, terpene-based resins, phenol-based resins, lavender-indene-based resins, and ketone resins can be used.

Examples of rosin-based resins include rosin derivatives such as disproportionated rosin, hydrogenated rosin, polymerized rosin, maleic rosin, and fumaric rosin, phenol-modified rosin, and rosin ester. Examples of phenol-modified rosins include those obtained by addition reaction of phenols with natural rosin or rosin derivatives, or phenol-modified rosins obtained by reacting resol-type phenol resins with natural rosin or rosin derivatives. Wait. As rosin ester, the esterification etc. which made the said rosin-type resin and polyhydric alcohol react, for example, are mentioned. Furthermore, the rosin phenol resin can also be made into an esterified product.

Examples of terpene resins include terpene resins (α-pinene resin, β-pinene resin, limonene resin, etc.), terpene phenol resin, aromatic modified terpene resin, hydrogenated terpene resin Wait.

Examples of petroleum resins include: aliphatic (C5 series) petroleum resins, aromatic (C9 series) petroleum resins, aliphatic/aromatic copolymer series (C5/C9 series) petroleum resins, and hydrogenated products of these (For example, an alicyclic petroleum resin obtained by hydrogenating an aromatic petroleum resin), various modified products of these (for example, maleic anhydride modified products), and the like.

Examples of phenol resins include condensation products of various phenols and formaldehyde, such as phenol, m-cresol, 3,5-xylenol, p-alkylphenol, and resorcinol. As other examples of phenol resins, resol resins obtained by the addition reaction of the above-mentioned phenols and formaldehyde under an alkali catalyst, or the condensation reaction of the above-mentioned phenols and formaldehyde under an acid catalyst can be mentioned. Novolac, etc. obtained.

Examples of lavender-indene resins include lavender-indene resins, hydrogenated lavender-indene resins, phenol-modified lavender-indene resins, epoxy-modified lavender-indene resins, etc. .

Examples of ketone resins include ketones (for example, aliphatic ketones such as methyl ethyl ketone and methyl isobutyl ketone; aromatic ketones such as acetophenone; aliphatic ketones such as acetophenone; or cyclohexane. A ketone resin obtained by condensation of ketone, methylcyclohexanone and other alicyclic ketones, etc.) with formaldehyde.

The softening temperature of the adhesive imparting resin used is not particularly limited. For example, an adhesive imparting resin with a softening point of 60°C to 160°C can be used. Moreover, it is also possible to use the adhesive imparting resin which is liquid at normal temperature. From the viewpoint of a well-balanced balance between cohesive force and low-temperature properties (such as unwinding or adhesion at low temperatures), a softening point of 60°C to 140°C (more preferably 80°C to 120°C) can be used Adhesion imparting resin. For example, it is preferable to use a petroleum resin having a softening point within the above range. Furthermore, the softening point of the adhesion imparting resin can be measured based on the softening point test method (Ring and Ball method) specified in JIS K2207.

The ratio of the polymer component contained in the adhesive layer to the adhesion-imparting resin is not particularly limited, and can be appropriately determined according to the application. Adhesion relative to 100 parts by weight of polymer components The content of the resin imparted on a non-volatile basis can be, for example, 20 parts by weight or more, and usually 50 parts by weight or more is appropriate. From the viewpoint of obtaining higher usage effects, the usage amount of the adhesion-imparting resin relative to 100 parts by weight of the polymer component can be 80 parts by weight or more, or 100 parts by weight or more. On the other hand, from the viewpoint of low-temperature characteristics and the like, it is generally appropriate to set the usage amount of the adhesion-imparting resin to 100 parts by weight of the polymer component to 200 parts by weight or less, and preferably to 150 parts by weight or less.

In addition, the above-mentioned adhesive layer may optionally contain viscosity modifiers (tackifiers, etc.), leveling agents, plasticizers, softeners, fillers, pigments or dyes and other colorants, light stabilizers, anti-aging agents, and anti-aging agents. Oxidizers, water resistant agents, antistatic agents, foaming agents, defoamers, surfactants, preservatives, cross-linking agents, etc. are various additives commonly used in the field of adhesives.

The formation of the adhesive layer can be carried out by appropriately using various previously known methods. For example, a method (direct method) of forming an adhesive layer by directly applying (typically coating) an adhesive composition on the substrate (typically a PVC film) as described above and drying it can be used. In addition, a method of forming an adhesive layer on the surface (peeling surface) and drying the adhesive composition due to the peelable surface (peeling surface) and transferring the adhesive layer to the substrate (transfer India and France). These methods can also be combined. As the above-mentioned release surface, the surface of the release liner or the back surface of the supporting substrate after release treatment can be used.

For coating the adhesive composition, for example, gravure roll coaters, reverse roll coaters, touch roll coaters, dip roll coaters, bar coaters, knife coaters, sprayers, etc. can be used. Or the usual coating machine. The adhesive layer is typically formed continuously, but according to the purpose or application, it may be formed in regular or irregular patterns such as dots and stripes.

Although not particularly limited, the thickness of the adhesive layer is typically 2 μm to 150 μm, usually 5 μm to 100 μm is appropriate, preferably 10 μm to 80 μm, and more preferably 10 μm to 50 μm (for example, 15 μm to 40 μm). The thickness range of the above-mentioned adhesive layer can be preferably applied to PVC adhesive tapes used in the protection or bundling of electric wires, piping, etc., the coating of corrugated pipes as described above, and electrical insulation.

<Adhesive Tape>

An example of the configuration of the adhesive tape disclosed here is shown in FIG. 1. The PVC adhesive tape 1 shown in FIG. 1 is configured as a single-sided adhesive tape, which includes: a supporting substrate (such as a single-layer PVC film) 11 having a first side 11A and a second side 11B, and a first side Adhesive layer 21 on surface 11A. In a preferred aspect, the adhesive tape 1 before use (that is, before attaching to the adherend) may be, for example, as shown in FIG. 1, which is wound on the second side of the supporting substrate by winding in the length direction. 11B abuts against the adhesive layer 21 to protect the surface (adhesive surface) 21A of the adhesive tape roll. Alternatively, it may be a form in which the surface 21A of the adhesive layer 21 is protected by a release liner whose at least the side facing the adhesive layer 21 becomes a release surface. As the release liner, a known or customary one can be used without particular limitation. For example, it can be used for a release liner with a release treatment layer on the surface of a substrate such as plastic film or paper, or a fluorine-based polymer (polytetrafluoroethylene, etc.) or polyolefin-based resin (polyethylene, polypropylene, etc.) Release liners of low adhesion materials, etc.

Another configuration example of the adhesive tape disclosed here is shown in FIG. 2. The adhesive tape shown in FIG. 2 is configured as a double-sided adhesive tape, which is provided with a first adhesive layer 21 and a second surface 11A and a second surface 11B of a supporting substrate (such as a single-layer PVC film) 11, respectively Two adhesive layer 22. The technology disclosed here can also be preferably implemented in the form of such a double-sided adhesive tape.

The adhesive tape disclosed here preferably has a heating loss of less than 4% measured by the following method. The adhesive tape with less heating loss has less plasticizer lost by volatilization, and less hydrogen chloride is generated along with the decomposition of PVC, so it has excellent heat-resistant deterioration. From the above viewpoint, the heating loss of the adhesive tape is preferably less than 3%, more preferably less than 2%, still more preferably less than 1.5%, and particularly preferably less than 1%. From the viewpoint of thermal degradation resistance, the closer the heating loss is to 0, the more advantageous. On the other hand, from the viewpoint of taking into account the heat-resistant degradation and other characteristics at a high level, the adhesive tape disclosed here can also have a heating loss of 0.3% or more (for example, 0.3% or more and less than 1.5%, more preferably 0.3% Above and less than 1.0%), or 0.5% or more (for example, 0.5% or more and less than 1%) is preferably implemented.

(Measurement method of heating loss)

The adhesive tape of the measuring object was cut into a size of 19 mm in width and 25 mm in length to prepare sample pieces. The weight of the above-mentioned sample piece was measured with a meter (Mettler Toledo, model "XP504DRV"), and the value was set to A. Then, the above-mentioned sample piece was placed in an aluminum schale (Gastec Service Company, No. 107), and put into a drying oven (ESPEC Company, PHH-20) set at 150°C for 240 hours. The heated adhesive tape was taken out from the drying oven, and the weight was measured using the above-mentioned meter (Mettler Toledo, XP504DRV). Set this value to B. According to the values A and B, the heating loss (%) is calculated by the following formula: (A-B)/A×100.

The adhesive tape disclosed here preferably has a retention force of 50 minutes or more measured by the following method. The adhesive tape with the above-mentioned holding power has moderate cohesiveness, so it has a good rationality during manufacture or use. From the above viewpoint, the holding power of the adhesive tape is more preferably 90 minutes or more, and even more preferably 120 minutes or more.

(Measurement method of retention)

It is measured according to the method described in JIS Z0237:2009. Specifically, the adhesive tape was allowed to stand at room temperature (23°C ± 2°C) for 1 hour, and then cut into a size of 10 mm in width and 100 mm in length. In order to suppress the elongation of the supporting base material caused by the load application as described below, a commercially available single-sided adhesive tape of the same size as the above was attached to the back of the adhesive tape for lining to prepare a measurement sample. As the above-mentioned commercially available single-sided adhesive tape, one that meets the following objectives can be selected: to suppress the elongation of the supporting substrate against the load, for example, the brand name "No. 31B" manufactured by Nitto Denko Corporation (with a thickness of 25μm) Ester film is used as a single-sided adhesive tape to support the substrate). One end of the short side of the measurement sample was crimped on a bakelite board (thickness 5mm, width 25mm, length 100mm) as the adherend by reciprocating a 2kg roller once so as to have a bonding area of 10mm wide and 20mm long. Attach a 300g weight to the other end of the short side of the measurement sample, keep the measurement sample level, and keep it at 40°C for 30 minutes. Then, under the same environment of 40°C, the above-mentioned bakelite board is held in such a way that the above-mentioned weight is located on the lower side and becomes a vertical direction, so that the measurement of the bakelite A given sample is given a load of 300g. Place it in this state, and measure the time (minutes) until the measured sample peels off the bakelite. Use this measured value as the holding force.

<Analysis>

The composition of the PVC adhesive tape or the PVC film constituting the adhesive tape in the technology disclosed herein can be analyzed using all analysis methods generally used in chemical analysis. Specifically, by appropriately combining analytical equipment or methods described in documents related to analytical chemistry, identification of each chemical species, identification of mixing amount or mixing ratio, and measurement of molecular weight can be performed. Hereinafter, suitable examples of the analysis method of the PVC adhesive tape and the PVC film disclosed herein will be described in more detail, but it is not intended to limit the scope of the present invention.

(1) Analysis method

(1-1) Preparation of samples used in analysis

As the sample used in the analysis, prepare the PVC adhesive tape according to the analysis method or the purpose of analysis, the PVC film used for the production of the adhesive tape, the separation of the above-mentioned adhesive tape into the supporting substrate (typically PVC film) and the adhesive Each solid sample of the agent, or the sample prepared by applying appropriate treatment to the sample, etc. Furthermore, a suitable example of the method of separating the PVC adhesive tape into the supporting substrate and the adhesive will be described later.

When a solution sample is required for analysis, for example, an appropriate solvent is added to the sample, and stirring or heating is performed as necessary to dissolve the components of the analysis object in the above solvent (typically extracted from the sample), This can prepare the above solution sample. As the solvent, considering the polarity and the like, it can be selected from chloroform (CHCl ₃ ), dichloromethane (CH ₂ Cl ₂ ), tetrahydrofuran (THF), acetone, dimethyl sulfide (DMSO), N,N-dimethyl Any one solvent of methylmethamide (DMF), methanol, ethanol, toluene, and water, or a mixed solvent of two or more of them in an arbitrary ratio.

As a solution sample, typically the following can be used: add about 30 mL of solvent to about 0.2 g sample (solid content), and stir in a temperature range from room temperature to about the boiling point of the solvent for about 30 minutes to 12 hours, Then dissolve the ingredients in the above sample to Solution in the above solvent. If necessary, for example, when the extraction efficiency of the components to be analyzed is low, the following operations can also be performed once or repeated multiple times to prepare a solution sample: add the newly added solution to the sample after the above solution is divided and the divided The solution is stirred with almost the same amount of solvent, and the solution is divided.

When it is necessary to adjust the concentration of the analysis target component contained in the solution sample obtained in this way, or when it is necessary to dissolve the analysis target component in a solvent with a different composition from the solvent used for extraction After evaporating part or all of the solvent contained in the above-mentioned solution sample, add the solvent corresponding to the objective composition and amount, thereby preparing the solution sample of the desired concentration or solvent composition.

In addition, when it is necessary to remove insoluble components from the solution sample, a solution sample in which the above-mentioned insoluble components have been removed can be obtained by filtering with a filter paper or a membrane filter.

When it is necessary to obtain a solution sample containing only a part of the type (typically a specific one or about 2 to 5 components) from a solution sample containing multiple components, in addition to using the following reference documents, etc. In addition to the purification or isolation of the column chromatography described, the following high performance liquid chromatography (HPLC) or gel permeation chromatography (GPC) can also be used to obtain the target solution sample.

(Reference literature)

The following, all edited by the Chemical Society of Japan, Maruzen Publishing House, 5th Edition Experimental Chemistry Lecture

Volume 8 NMR. ESR (issued in 2006)

Volume 9 The Structure of Matter I (issued in 2005)

Volume 10 The Structure of Matter II (issued in 2005)

Volume 20-1 Analytical Chemistry (issued in 2007)

Volume 20-2 Environmental Chemistry (issued in 2007)

Volume 26 Polymer Chemistry (issued in 2005)

(1-2) Method of separating PVC adhesive tape into supporting substrate and adhesive

The method of separating the PVC adhesive tape into the supporting substrate and the adhesive is not particularly limited. Make For a simple and convenient method, the following method can be used: the PVC adhesive tape is bent so that the adhesive layer becomes the inner side, the adhesive layers are attached to each other, and then peeled off, so as to be located on the side of the bent The method of transferring the adhesive layer to the adhesive layer on the other side. By transferring the adhesive layer on one side to the adhesive layer on the other side, the adhesive layer can be removed from the supporting substrate on this side. The two adhesive layers overlapped on the other side can be further overlapped by repeating the same bending and peeling as necessary. According to this method, the self-adhesiveness of the adhesive can be used to separate the support substrate and the adhesive without the use of organic solvents or heat treatment. Therefore, the composition of the adhesive tape can be analyzed with high precision. Furthermore, regarding conditions such as the time to peel off after the adhesive layers are attached to each other, the speed of peeling, and the peeling angle, the industry can appropriately set a way to easily transfer the adhesive layer. In addition, by bonding the adhesive layers of two PVC adhesive tapes to each other instead of bending and peeling one PVC adhesive tape, the adhesive layer of one adhesive tape can also be transferred to the adhesive layer of the other adhesive tape. on.

(1-3) Fourier transform infrared spectroscopic analysis (FT-IR)

The Fourier transform infrared spectroscopic analysis of the solid sample or the solid sample obtained by removing the solvent from the solution sample can be performed by ATR (attenuated total reflection) method using the following equipment and conditions. By using this analysis method alone or in combination with other analysis methods, the composition of the components contained in the PVC adhesive tape or its adhesive layer can be identified and the composition ratio can be calculated.

(Device and conditions)

Device: Thermo Fisher Scientific, Nicolet 6700

Condition: One-time reflection ATR method (Smart iTR, Ge45°)

Resolution: 4cm ^-1

Detector: DTGS

Cumulative times: 64 times

(1-4) Fourier transform nuclear magnetic resonance spectroscopic analysis (FT-NMR)

The solid sample or the solid sample obtained by removing the solvent from the solution sample can be dissolved in any deuterated solvent (CDCl ₃ , CDCl ₂ , THF-d8, acetone-d6, DMSO-d6, DMF-d7, Methanol-d4, ethanol-d6, D ₂ O, etc.), and use the following equipment and conditions to provide Fourier transform nuclear magnetic resonance spectroscopy ( ¹ H-NMR and/or ¹³ C-NMR). In the analysis, a sample whose concentration has been adjusted so that 0.1 g of a deuterated solvent becomes 0.06 to 6 mL with respect to a solid sample can be used. By using this analysis method alone or in combination with other analysis methods, the composition of the components contained in the PVC adhesive tape or its adhesive layer can be identified and the composition ratio can be calculated.

(Device and conditions)

Device: Brook Byerspin, AVANCE III-600, with Cryo Probe

Observation frequency: 600MHz ( ¹ H), 150MHz ( ¹³ C)

Measuring temperature: 300K

(1-5) Gas chromatography/mass spectrometry (GC/MS)

The gas chromatography/mass spectrometry analysis of the above solution sample can be performed using the following equipment and conditions. The concentration of the above-mentioned solution sample can be adjusted appropriately so that the solvent becomes 0.6 to 60 mL with respect to 0.1 g of the solid sample, and it can be used as a sample for analysis. By using this analysis method alone or in combination with other analysis methods, the composition of the components contained in the PVC adhesive tape or its adhesive layer can be identified and the composition ratio can be calculated. Furthermore, with regard to the components of the identified peaks in the peaks appearing in the chromatogram, a calibration curve is made using the identified substance or a compound with a molecular structure similar to the identified substance as a standard, so that the identified composition can be calculated in the test The content in the sample.

(Device and conditions)

Device: ThermoFinigan, Trace GC ultra (GC), Polaris Q (MS)

GC conditions

×30m) . Column: Ultra ALLOY-5 (0.25μm, 0.25mm

×30m)

. Carrier gas: He(1.0mL/min)

. Note inlet: split flow (split ratio 50:1)

. Note inlet temperature: 250℃

. Column temperature: 40℃(3min)→(+20℃/min)→300℃(24min)

MS conditions

. Ionization method: Choose EI, FI or CI appropriately

. Electron energy: 70eV

. Ion source temperature: 210℃

. Interface temperature: 300℃

. Mass range: m/z=20~800

(1-6) Gas Chromatography (GC)

The gas chromatography method of the above solution sample can be performed using the following equipment and conditions. The concentration of the above-mentioned solution sample can be adjusted appropriately so that the solvent becomes 0.6 to 60 mL with respect to 0.1 g of the solid sample, and it can be used as a sample for analysis. By using this analysis method alone or in combination with other analysis methods, the composition of the components contained in the PVC adhesive tape or its adhesive layer can be identified and the composition ratio can be calculated. Furthermore, with regard to the peaks that constitute the identified components in the peaks appearing in the chromatogram, a calibration curve is prepared using the identified substance or a compound with a molecular structure similar to the identified substance as a standard, so that the above identified The content of the ingredients in the sample.

(Device and conditions)

Device: Agilent Technologies, 6890Plus

Column: HP-1, 30m×0.250mm inner diameter×1.0μm film thickness

Column temperature: 100℃→(+20℃/min)→300℃(maintain)

String pressure: 101.7kPa (constant current mode)

Carrier gas: He(1.0mL/min)

Note inlet: split flow (split ratio 20:1)

Note inlet temperature: 250℃

Detector: FID

Detector temperature: 250℃

Injection volume: 1μL

(1-7) Liquid chromatography/Fourier transform mass spectrometry (LC/FT-MS)

The liquid chromatography/Fourier transform mass spectrometry analysis of the above solution sample can be performed using the following equipment and conditions. The concentration of the above-mentioned solution sample can be adjusted appropriately so that the solvent becomes 0.6 to 60 mL with respect to 0.1 g of the solid sample, and it can be used as a sample for analysis. By using this analysis method alone or in combination with other analysis methods, the composition of the components contained in the PVC adhesive tape or its adhesive layer can be identified and the composition ratio can be calculated. Furthermore, with regard to the peaks that constitute the identified components in the peaks appearing in the chromatogram, a calibration curve is prepared using the identified substance or a compound with a molecular structure similar to the identified substance as a standard, so that the above identified The content of the ingredients in the sample.

(Device and conditions)

Device: Thermo Fisher Scientific, UltiMate 3000 (LC), LTQ orbitrap XL (FT-MS)

LC conditions

×100mm，1.8μm) . Column: Agilent Technologies Zorbax Eclipse PlusC8 (3.0mm

×100mm, 1.8μm)

. Eluent composition: ACN (acetonitrile)/ammonium acetate aqueous solution gradient

. Flow rate: 0.5mL/min

. Column temperature: 40℃

Injection volume: 5μL

FT-MS conditions

. Ionization method: ESI (negative, positive)

. Ion spray voltage: 3kV

(1-8) High performance liquid chromatography (HPLC)

The high performance liquid chromatography method of the above solution sample can be performed using the following equipment and conditions. The concentration of the above-mentioned solution sample can be adjusted appropriately so that the solvent becomes 0.6 to 60 mL with respect to 0.1 g of the solid sample, and it can be used as a sample for analysis. By using this analysis method alone or in combination with other analysis methods, the composition of the components contained in the PVC adhesive tape or its adhesive layer can be identified and the composition ratio can be calculated. Furthermore, with regard to the peaks that constitute the identified components in the peaks appearing in the chromatogram, a calibration curve is prepared using the identified substance or a compound with a molecular structure similar to the identified substance as a standard, so that the above identified The content of the ingredients in the sample. In addition, by separating the eluates corresponding to the peaks in the chromatogram, the components contained in the adhesive tape can be separated as a single component or a more simplistic mixture, and the separated can also be used as an analysis The sample is also used in other analysis methods.

(Device and conditions)

Device: Agilent Technologies, 1100

×150mm，5μm) Column: Inertsil C8-4 (4.6mm

×150mm, 5μm)

Composition of the lysate: gradient conditions of distilled water/acetonitrile

Flow rate: 1.0mL/min

Detector: DAD (190~400nm, 230nm detection)

Column temperature: 40℃

Injection volume: 10μL

(1-9) Gel Permeation Chromatography (GPC)

The gel permeation chromatography method of the above solution sample can be performed using the following equipment and conditions. The concentration of the above-mentioned solution sample can be appropriately adjusted so that 1 mg of the solvent of the solid sample becomes 0.1 to 10 mL, and this can be used as an analysis sample. The sample for analysis is filtered with an appropriate filter (for example, a membrane filter with an average pore diameter of about 0.45 μm) and injected into the device. By this analysis, the molecular weight of the peak appearing in the chromatogram can be used as the following standard Calculated based on the value of quasi-polystyrene conversion. In addition, by separating the eluates corresponding to the peaks in the chromatogram, the components contained in the adhesive tape can be separated as a single component or a more simplistic mixture, and the separated can also be used as an analysis The sample is also used in other analysis methods.

(Device and conditions)

Device: Tosoh Corporation, HLC-8120GPC

Pump: Enshine Scientific Corporation, CO-150

Pump flow rate: 1mL/min

Column: Tosoh Corporation, used by connecting HXL Guard Column, TSKgel G4000HXL, TSKgel G5000HXL, TSKgel GMHXL mixed-bed

Column oven temperature: 40℃

Detector: manufactured by Shimadzu Corporation, differential refractive index detector RID-10A

Developing solvent: THF

Injection volume: 100μL

Standard polystyrene: Tosoh Corporation, TSK gel standard polystyrene F-288, TSK gel standard polystyrene F-40, TSK gel standard polystyrene F-4, TSK gel standard polystyrene A-5000 , TSK gel standard polystyrene A-500

(2) Analysis of plasticizer

(2-1) Quantitative analysis by ¹ H-NMR

0.2 g of the supporting substrate (typically PVC film) obtained by removing the adhesive from the PVC adhesive tape by the method in (1-2) above was immersed in 30 mL of chloroform, and stirred at room temperature for 30 minutes, and then Dispense the solution. The supporting substrate was immersed in new 30 mL of chloroform and stirred at room temperature for 30 minutes, then the solution was divided, and this operation was repeated twice. In this way, 90 mL of the chloroform solution containing the plasticizer in the supporting substrate was recovered. To the solid content obtained by evaporating chloroform from the solution, CDCl ₃ is added so as to become the concentration described in (1-4) above to obtain a sample for analysis.

The ¹ H-NMR measurement was performed by the apparatus and conditions described in (1-4) above. Calculate the peaks derived from the plasticizer by referring to the obtained spectrum and the results obtained by other analysis methods, and calculate the content of the plasticizer from the integral ratio of these peaks. When the sample for analysis contains two or more plasticizers, the content of each plasticizer is calculated in the same manner. Furthermore, when the peak derived from a certain plasticizer overlaps with the peak derived from other components (other plasticizers or components other than plasticizers), calculate the integral ratio after removing the contribution of the other components Show the content of the plasticizer.

(2-2) Molecular weight analysis by GPC

90 mL of the chloroform solution from which the plasticizer in the support substrate was extracted was recovered by the same operation as in (2-1) above. The chloroform solution recovered in (2-1) above can also be used in this analysis. To the solid content obtained by evaporating chloroform from this solution, THF is added so as to become the concentration described in (1-9) above to obtain a sample for analysis.

The analysis sample was analyzed by the apparatus and conditions described in (1-9) above to obtain a chromatogram. With reference to the obtained chromatogram and the results obtained by other analysis methods, the peak derived from the plasticizer is identified from the above chromatogram. The line connecting the two foothills of the peak (the vicinity where the peak starts to rise and the vicinity where it converges) is used as the reference line to obtain the molecular weight of the plasticizer. When the sample for analysis contains two or more plasticizers, the molecular weight of each plasticizer is calculated in the same manner.

(2-3) Allocation amount and allocation ratio of PLH and PLL

The allocation amount of PLH and PLL (W _PLH , W _PLL ) and the weight-based allocation ratio (W _PLH /W _PLL ) are calculated as follows.

(i) The plasticizer (PLL, PLH) is extracted from the supporting substrate by the method described in (2-1) above. At this time, the weight of the solvent-insoluble matter and the weight of the solvent-soluble matter (that is, the extract obtained by the solvent) are separately measured.

(ii) For the above extract, the ¹ H-NMR and ¹³ C-NMR of (1-4) above or the analysis described in (1-3), (1-5), (1-7) above are appropriately used Method, the chemical structure of the components contained in the extract is identified, and the formula weight (molecular weight) is calculated. For specific chemical structures, publicly known atlas data sets can be used as needed.

(iii) In the ¹ H-NMR spectrum of (1-4) above, calculate the molar ratio of each component from the number of protons (integration ratio) derived from the PLH, PLL, and other components contained in the above extract . By applying the formula weight obtained in (ii) above to the result, the weight ratio of each component can be calculated. The blending ratio (W _PLH /W _PLL ) is obtained from this weight ratio.

(iv) Calculate the weight ratio of PLH and PLL to the total weight of the supporting substrate from the weight ratio of (i) and (iii) above.

Depending on the situation, as another method, it is also possible to apply the molecular weight of each component grasped by the GPC of (2-2) to each component calculated from the integral ratio in the ¹ H-NMR spectrum of (ii) Calculate the allocation ratio (W _PLH /W _PLL ) based on the molar ratio.

As another method, in the analysis of (1-7) in (ii) above, when PLH and PLL can be separated with high accuracy (when the peaks of these components are well separated), the above ( Separate PLH and PLL by the method described in 1-8), and calculate the blending ratio (W _PLH /W _PLL ) from the dry weight of these.

Furthermore, the molecular weight of the plasticizer used in the production of PVC film (the plasticizer before use, that is, the plasticizer raw material) can be replaced by, for example, an analytical sample prepared by directly dissolving the above plasticizer raw material in THF The analysis sample of (2-2) above was obtained by extracting the plasticizer in the supporting base material. In more detail, it can be prepared by dissolving the above-mentioned plasticizer raw material in THF at the concentration described in (1-9) above (for example, 10 mg of the plasticizer raw material, a concentration of 10 mL of THF) in THF The sample is analyzed by the apparatus and conditions described in (1-9) above to obtain a chromatogram, and the molecular weight is determined from the chromatogram in the same manner as in (2-2) above. Although there is no particular limitation, a PVC film that satisfies the preferred blending ratio (W _PLH /W _PLL ) disclosed herein can be obtained, for example, by the following method: a plasticizer classified as PLH is selected based on the molecular weight mastered by the above method And classified as PLL plasticizer, and according to the desired W _PLH / W _{PLL to} mix these. However, the description in this paragraph is only an example, and does not limit the scope of the invention disclosed herein.

(3) Analysis of antioxidants

(3-1) Composition analysis

90 mL of the chloroform solution from which the antioxidant in the support substrate was extracted was recovered by the same operation as in (2-1) above. The chloroform solution recovered in (2-1) or (2-2) above can also be used in this analysis. Use this chloroform solution, and apply one or a combination of two or more appropriate analytical methods from the above-mentioned HPLC, FT-IR, ¹ H-NMR, ¹³ C-NMR and LC/FT-MS to identify antioxidants And conduct composition analysis.

(3-2) Quantitative analysis

0.2 g of the supporting substrate (typically a PVC film) obtained by removing the adhesive from the PVC adhesive tape was immersed in 30 mL of THF, and stirred at room temperature for 30 minutes, and then the solution was divided. The supporting substrate was immersed in new 30 mL of THF, and stirred at room temperature for 30 minutes, and then the solution was divided, and this operation was repeated twice. In this way, 90 mL of the THF solution from which the antioxidant in the support substrate was extracted was recovered. The reprecipitation operation was performed by adding the THF solution to 100 times the amount of the THF solution (volume basis) in methanol, and the supernatant was filtered with a membrane filter, and then analyzed by HPLC to obtain chromatography Figure. Using the antioxidant-derived peak appearing in the chromatogram, the antioxidant specified by the above composition analysis was used as a standard to prepare a calibration curve to quantify the antioxidant.

(4) Analysis of fatty acid metal salt

Qualitative analysis of the metal species constituting the fatty acid metal salt can be performed by fluorescent X-ray analysis (XRF) using the following equipment and conditions. Specifically, the adhesive surface of the PVC adhesive tape (the surface of the adhesive layer) was attached to a filter paper with a diameter of 20 mm, and X-rays were irradiated from the supporting substrate side.

(Device and conditions)

Device: Rigaku Corporation, ZSX100e

X-ray source: vertical Rh tube

Analysis element: B~U

Analysis area: 20mm

X-ray output and spectroscopic crystal: as shown in Table 1.

<Use>

Since the adhesive tape disclosed here is excellent in heat deterioration resistance, it can be used in various fields requiring heat resistance. For example, it is suitable for the protection or bundling of electric wires and piping, covering and electric insulation of corrugated pipes that surround electric wires and the like for protection. Among them, preferred applications include bundling or fixing of wiring harnesses (such as wiring harnesses for automobiles and other vehicles, especially wiring harnesses for vehicles with internal combustion engines, etc.), and covering or bundling and fixing wiring harness corrugated pipes. The purpose of winding around the wires (typically a plurality of wires) constituting the wire harness. Here, in the case where the adhesive tape is wound around the wire constituting the wire harness, it includes the case where the adhesive tape is wound around the wire, or around the tube (such as a corrugated tube) containing the above-mentioned wire It is wrapped with adhesive tape. In addition, the adhesive tape disclosed here is not limited to the above-mentioned uses, and can also be used in various fields where PVC adhesive tape has been previously used, such as insulation, fixing, and fixing between layers or outer surfaces of electrical parts (transformers, coils, etc.), electronic parts, etc. Appropriate use in fields such as display and identification.

The matters disclosed in this manual include the following.

(1) An adhesive tape comprising: a polyvinyl chloride film containing a plasticizer, and an adhesive layer arranged on at least one surface of the film, The heating loss is less than 4%, and the holding power is more than 50 minutes.

(2) The adhesive tape of (1) above, wherein the content of the plasticizer in the polyvinyl chloride film is about 10-50% by weight.

(3) The adhesive tape according to (1) or (2) above, wherein the polyvinyl chloride film contains a fatty acid metal salt.

(4) The adhesive tape of (3) above, wherein the fatty acid metal salt contains any one of Group 1, Group 2, Group 12, Group 13 and Group 14 (excluding Pb) of the periodic table At least one metal element.

(5) The adhesive tape of (3) or (4) above, wherein the fatty acid metal salt contains at least one metal element selected from the group consisting of Li, Na, Ca, Mg, Zn, Ba, and Sn.

(6) The adhesive tape of any one of (3) to (5) above, wherein the fatty acid metal salt is a metal stearate, a metal laurate, or a combination of a metal stearate and a metal laurate .

(7) The adhesive tape of any one of (3) to (6) above, wherein the content of the fatty acid metal salt in the PVC film is about 0.02% by weight or more and about 1% by weight or less.

(8) The adhesive tape according to any one of (1) to (7) above, wherein the polyvinyl chloride film contains an antioxidant (for example, a hindered phenol-based antioxidant).

(9) The adhesive tape of the above (8), wherein the content of the antioxidant in the PVC film is about 0.05% by weight or more and about 10% by weight or less.

(10) The adhesive tape of any one of (1) to (9) above, wherein the polyvinyl chloride film contains a polyester plasticizer with a molecular weight of 1,000 or more and a carboxylic acid ester with a molecular weight of less than 1,000 as the plasticizer Agent.

(11) The adhesive tape of (10) above, wherein for the polyvinyl chloride film, the weight of the polyester plasticizer with a molecular weight of 1,000 or more contained in the film W _PLH and the weight of the polyester plasticizer contained in the film The relationship between the weight W _PLL of the above-mentioned carboxylic acid ester with a molecular weight of less than 1000 satisfies the following formula: 1≦(W _PLH /W _PLL )≦50.

(12) The adhesive tape of the above (10) or (11), wherein the carboxylic acid ester having a molecular weight of less than 1,000 includes an aromatic carboxylic acid ester.

(13) The adhesive tape of (12) above, wherein the aromatic carboxylic acid ester includes at least one of trimellitate and pyromellitic acid ester.

(14) The adhesive tape according to any one of (10) to (13) above, wherein the carboxylic acid ester with a molecular weight of less than 1000 includes an ester of a carboxylic acid and an alkyl alcohol having 6 to 14 carbon atoms.

(15) The adhesive tape of any one of the above (10) to (14), wherein the content of the carboxylic acid ester with a molecular weight of less than 1000 in the PVC film is about 0.5% by weight or more (preferably about 1% by weight) % Or more, more preferably about 2% by weight or more) and about 25% by weight or less (preferably about 20% by weight or less, more preferably about 15% by weight or less).

(16) The adhesive tape according to any one of (10) to (15) above, wherein the polyester plasticizer with a molecular weight of 1,000 or more includes an adipic acid polyester plasticizer.

(17) The adhesive tape according to any one of (10) to (16) above, wherein the polyester plasticizer having a molecular weight of 1,000 or more includes an adipic acid polyester plastic having a molecular weight of about 2500 or more and about 7000 or less.化剂。 Chemical agent.

(18) The adhesive tape according to any one of the above (10) to (17), wherein the content of the polyester plasticizer with a molecular weight of 1000 or more in the PVC film is about 3% by weight or more (preferably about 5% by weight or more, more preferably about 10% by weight or more) and about 35% by weight or less (preferably about 30% by weight or less, more preferably about 25% by weight or less).

(19) The adhesive tape according to any one of (1) to (18) above, wherein the polyvinyl chloride film contains an elastomer.

(20) The adhesive tape of (19) above, wherein the content of the elastomer in the PVC film is about 1% by weight or more and about 30% by weight or less.

(21) The adhesive tape of the above (19) or (20), wherein the elastomer contains one or two or more selected from the following compounds: (A) Chlorinated polyethylene with a chlorine content of about 25-50% by weight (e.g. about 35-45% by weight), (B) (meth)acrylate-butadiene-styrene copolymer, (C) propylene An acrylonitrile-butadiene copolymer with a nitrile content of about 15-50% by weight (e.g., about 30-40% by weight), and (D) a vinyl acetate content of about 30-75% by weight (e.g., about 50-65% by weight) %) of ethylene-vinyl acetate copolymer.

(22) The adhesive tape of any one of (1) to (21) above, wherein the adhesive layer is a rubber-based adhesive layer with a rubber-based adhesive as a main component.

(23) The adhesive tape of any one of (1) to (22) above, wherein the adhesive layer contains natural rubber and synthetic rubber (such as SBR) in a weight ratio of about 10:90 to 90:10.

(24) The adhesive tape of any one of (1) to (23) above, wherein the adhesive layer contains a resin selected from the group consisting of rosin resin, petroleum resin, terpene resin, phenol resin, and lavender carbo-indene resin. One or more of resins and ketone resins for adhesion imparting resins.

(25) The adhesive tape of any one of (1) to (24) above, wherein the adhesive layer contains a rubber-based polymer and an adhesion-imparting resin, The content of the adhesion imparting resin is about 50 to 150 parts by weight relative to 100 parts by weight of the rubber-based polymer.

(26) A wire harness comprising an electric wire and the adhesive tape of any one of (1) to (25) above wound around the electric wire.

Example

Hereinafter, some embodiments of the present invention will be described, but the present invention is not intended to be limited to those shown in the specific example. In addition, "parts" and "%" in the following descriptions are based on weight unless otherwise specified.

<Use materials>

The materials used in the following examples and their symbol numbers are as follows.

(Polyvinyl chloride (PVC))

A: Shin-Etsu Chemical Co., Ltd. product, polymerization degree 1300, trade name "TK-1300"

B: Product of Shin-Etsu Chemical Co., Ltd., polymerization degree 1400, trade name "TK-1400"

(Antioxidants)

A: BASF company product, phenolic antioxidant, trade name "Irganox 1010"

(Fatty acid metal salt)

A: Calcium stearate (product of Kishita Chemical Co., Ltd.)

B: Zinc laurate (product of Sanjinhe Chemical Co., Ltd.)

(Plasticizer)

H1: Product of DIC Co., Ltd., adipic acid-based polyester plasticizer, trade name "W-360ELS", molecular weight 2800 (based on the value measured by the above method)

H2: Product of DIC Co., Ltd., adipic acid-based polyester plasticizer, trade name "W-2300", molecular weight 3200 (measured value based on the above method)

H3: Product of DIC Co., Ltd., adipic acid-based polyester plasticizer, trade name "W-4010", molecular weight 5800 (based on the value measured by the above method)

L1: J-PLUS Co., Ltd. product, diisononyl phthalate, trade name "DINP", molecular weight 504 (value based on the above method)

L2: DIC Co., Ltd. product, tri-n-octyl trimellitate, trade name "W-755", molecular weight 750 (based on the value measured by the above method)

L3: DIC Co., Ltd. product, tris(2-ethylhexyl) trimellitate, trade name "W-705", molecular weight 750 (based on the value measured by the above method)

L4: Kao Co., Ltd. product, triisodecyl trimellitate, trade name "TRIMEX T-10", molecular weight 810 (measured based on the above method)

L5: Product of ADEKA Co., Ltd., pyromellitic acid tetrakis (2-ethylhexyl) Ester, trade name "UL-80", molecular weight 834 (based on the value measured by the above method)

(Elastomer)

A: Showa Denko Co., Ltd. product, chlorinated polyethylene, trade name "ELASLEN 301A"

B: Product of Nippon Synthetic Chemical Industry Co., Ltd., ethylene-vinyl acetate copolymer, trade name "Soarblen BH"

<Making of Adhesive Tape>

(Example 1)

Based on the solid content basis, 60 parts of SBR latex (product of Zeon Corporation, trade name "Nipol LX426"), 40 parts of natural rubber latex (product of GOLDEN HOPE company, trade name "HYTEX HA") and 120 petroleum resin emulsion The parts are mixed to prepare a water-dispersed rubber-based adhesive composition. As the above-mentioned petroleum resin emulsion, 75 parts of petroleum resin (product of EXXON, aliphatic hydrocarbon resin, trade name "ESCOREZ 1202", softening point 100°C) was dissolved in 25 parts of toluene, and a surfactant ( Product of Kao Co., Ltd., trade name "EMULGEN 920") 3.5 parts and 46.5 parts of water, mixed and emulsified with a homomixer. Hereinafter, the above-mentioned adhesive composition is referred to as "adhesive composition A".

The raw materials shown in Table 2 are made into the composition shown in Table 2 (that is, antioxidant A is contained at a rate of 0.05% by weight, fatty acid metal salt A is contained at a rate of 0.10% by weight, and plastic is contained at a rate of 26% by weight. The chemical agent H3, the plasticizer L2 at a ratio of 6% by weight, and the remainder containing polyvinyl chloride A) are measured and mixed. After kneading, they are formed into a thickness of 100μm at a molding temperature of 150°C using a calender molding machine. Long film shape. In this way, the PVC film of Example 1 was obtained.

Using a comma direct coater, apply the adhesive composition A to one surface of the PVC film, and dry it, and take it up to a sufficient length for the following winding test . The coating amount of adhesive composition A is dry Adjust the thickness of the adhesive layer to be formed later to 20μm. It was cut into a width of 19 mm (cut into a long strip) to obtain the adhesive tape of Example 1 having an adhesive layer on one surface of the PVC film.

(Examples 2 to 11 and Comparative Examples 1 to 2)

The composition of the PVC film, the thickness of the PVC film, and the thickness of the adhesive layer were set as shown in Table 2. Except for this, in the same manner as in Example 1, Examples 2 to 11 and Comparative Examples 1 to 2 were produced. The adhesive tape.

<Measurement and Evaluation>

(Heat loss)

According to the above heating loss measurement method, the heating loss of the adhesive tape of each case was measured. The results obtained are shown in Table 2.

(Retentivity)

According to the above-mentioned retention force measurement method, the retention force of the adhesive tape of each case was measured. The results obtained are shown in Table 2.

(Initial adhesion)

Cut the adhesive tape (width 19mm) of each example to an appropriate length, and press a 2kg roller back and forth at 23°C and 50% RH to crimp the stainless steel plate (SUS plate) as the adherend. Place it in an environment of 23°C and 50%RH for 30 minutes, and then measure the 180-degree peel strength (N/19mm) at a tensile speed of 300mm/min using a tensile testing machine in accordance with JIS Z0237:2009. The results obtained are shown in Table 2.

(Winding test)

10mm)之長度600mm之範圍內，藉由半搭接(half lap)而纏繞各例之黏著帶(寬19mm)，製作評價用之樣品。此處所謂半搭接，係指於纏繞黏著帶時，以該黏著帶之寬度之一半重疊於已纏繞之黏著帶之寬度之一半之方式進行之纏繞態樣。將上述樣品投入至設定為105 ℃之吉爾烘箱(Geer oven)(東洋精機公司，ACR60)中保持3000小時。其後，將上述樣品自吉爾烘箱中取出，放置於室溫(25±3℃)下，於樣品之溫度等同於室溫後，以沿著100mm徑之鋼棒之外周之方式進行纏繞。維持該狀態，纏繞於鋼棒外周30分鐘後，藉由目視觀察樣品之外觀。具體而言，觀察有無龜裂(纏繞於波紋管之黏著帶中產生電裂之狀態)、及於黏著帶之開始纏繞及結束纏繞之端部有無自波紋管之剝落。 Corrugated pipe for protecting vehicle wiring harness (manufactured by Yazaki Corporation, HCOT-FR,

The adhesive tape (width 19mm) of each example was wound by half lap within the range of 600mm in length of 10mm) to prepare samples for evaluation. The so-called semi-lap joint here refers to the winding state in which half of the width of the adhesive tape overlaps with half of the width of the wound adhesive tape when the adhesive tape is wound. The above-mentioned sample was put into a Geer oven (Toyo Seiki Co., Ltd., ACR60) set at 105°C and kept for 3000 hours. After that, the above-mentioned sample was taken out of the Geer oven and placed at room temperature (25±3°C). After the temperature of the sample was equal to room temperature, it was wound along the outer circumference of a steel rod with a diameter of 100 mm. Maintaining this state, after winding around the outer circumference of the steel bar for 30 minutes, the appearance of the sample was observed visually. Specifically, observe whether there is a crack (a state where electric cracks are generated in the adhesive tape wound around the corrugated tube), and whether there is peeling off the corrugated tube at the beginning and end of the winding of the adhesive tape.

The observation results are shown in Table 2 according to the following three levels.

◎: No cracks and end peeling were found (excellent).

○: Slight cracks are found, but the outer surface of the bellows is not seen, and no end peeling is found (good).

×: Cracks at the level of the outer surface of the bellows are seen, and peeling at the ends is also found (poor).

According to the results of the winding test shown in Table 2, it can be seen that the adhesive tapes of Examples 1 to 11 whose heating loss is suppressed to less than 4% are compared with the adhesive tapes of Comparative Examples 1 to 2 whose heating loss is more than 4%. Obviously good heat deterioration resistance. The adhesive tapes of Examples 1-7, 10, and 11 containing PLH and PLL in a weight ratio of 0.5-100 with W _PLH /W _PLL showed particularly good heat-resistant deterioration. Furthermore, it can be seen that although the adhesive tape of Example 8 exhibits performance equivalent to or higher than that of Examples 1 to 7, 10, and 11 in terms of heat degradation resistance, the flexibility at low temperatures is slightly insufficient.

The specific examples of the present invention have been described in detail above, but these are only examples and do not limit the scope of patent applications. The technology described in the scope of the patent application includes various changes and modifications to the specific examples illustrated above.

1‧‧‧PVC Adhesive Tape

11‧‧‧Support substrate

11A‧‧‧The first side

11B‧‧‧Second side

21‧‧‧Adhesive layer

21A‧‧‧Surface (adhesive surface)

Claims (7)

An adhesive tape comprising: a polyvinyl chloride film containing a plasticizer and an adhesive layer arranged on at least one surface of the film, the heating loss is less than 4%, and the retention force is more than 50 minutes. Containing a polyester plasticizer with a molecular weight of 1,000 or more and a carboxylic acid ester with a molecular weight of less than 1,000 as the plasticizer, and for the polyvinyl chloride film, the polyester with a molecular weight of 1,000 or more contained in the film The relationship between the weight of the plasticizer W _PLH and the weight of the above-mentioned carboxylic acid ester with a molecular weight of less than 1000 contained in the film W _PLL satisfies the following formula: 1≦(W _PLH /W _PLL )≦50. The adhesive tape of claim 1, wherein the polyvinyl chloride film contains fatty acid metal salt. Such as the adhesive tape of claim 2, wherein the fatty acid metal salt contains at least one metal belonging to any one of Group 1, Group 2, Group 12, Group 13 and Group 14 (except Pb) of the periodic table element. The adhesive tape of claim 2, wherein the fatty acid metal salt contains at least one metal element selected from the group consisting of Li, Na, Ca, Mg, Zn, Ba, and Sn. The adhesive tape of any one of claims 1 to 4, wherein the polyvinyl chloride film contains an antioxidant. The adhesive tape according to any one of claims 1 to 4, wherein the polyvinyl chloride film contains an elastomer. A wire harness comprising an electric wire and an adhesive tape such as any one of claims 1 to 6 wound around the electric wire.

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