WO2009069485A1 - エラストマー偏在ポリマー層を有する粘弾性部材 - Google Patents
エラストマー偏在ポリマー層を有する粘弾性部材 Download PDFInfo
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- WO2009069485A1 WO2009069485A1 PCT/JP2008/070832 JP2008070832W WO2009069485A1 WO 2009069485 A1 WO2009069485 A1 WO 2009069485A1 JP 2008070832 W JP2008070832 W JP 2008070832W WO 2009069485 A1 WO2009069485 A1 WO 2009069485A1
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Definitions
- rubber-based and acrylic-based polymers are widely used for sheet fills and cushioning materials.
- the rubber-based rill system has its pros and cons, and it is used according to the purpose.
- adhesive tape or sheet tape or sheet may be simply or sheet
- one of the materials, such as polio fin is the material, such as metal.
- rubber acrylic It is required to have a length.
- rubber-based materials and acryl polymers are blended (, patents
- this blend can be used to improve adhesion to the acrylic system, this blend is made transparent due to the nature of the rubber system and the acrylic polymer. However, there were thoughts such as the fact that there was not enough, and the change in the performance of the preservation from the body production.
- the law requires a different manufacturing process.
- 008 exhibits different properties on the other side of the bright side, and has a transparent appearance and less dyeing.
- the object of the present invention is to provide a layered structure with a polymer polymer having a last polymer polymer that can control the cloth of the polymer in the layer and has excellent adhesion to the polymer polymer having the last polymer layer.
- a polymerizable monomer composed of a polymerizable substance containing at least a polymerizable monomer last is provided on both sides of the monomer capable of absorbing the polymerizable monomer.
- the last polymer moves and the last polymer is obtained.By polymerizing the last polymer, the layer structure with the last polymer monomer is obtained, and in the polymer layer in the last layer polymer layer. They found that the surface opposite to the noma is in the vicinity of the surface and completed the statement.
- poly has a layer structure that absorbs at least some kinds of components constituting the poly, and the poly layer is distributed in the vicinity of the surface opposite to the object. It is characterized in that it is a last polymer layer that includes a last in form.
- the cover fill is laminated on the opposite side.
- the vicinity of the surface opposite to the monomer in 00112 is a region within 5 with respect to the direction from the surface opposite to the monomer.
- the polymer of the monopolymer layer may be an acrylic polymer.
- the monomer component constituting the polymer of the monomer polymer layer is an elastomer polymer. It may be common with any one of the components constituting the poly, and may be mono-adhesive.
- the poly of the elasto poly layer is preferably an acrylic poly.
- the elastomer is a styrene elastomer.
- the elastomeric polymer layer is mono
- It may be a polymer layer in which the last adhesion is present in a form that is distributed in the vicinity of the opposite surface to that of the last. It is preferable that the polymer of the existing poly layer is not attached. No. of last poly layer at 008
- the surface on the opposite side may be sticky.
- 00 9 Tape Can have a sheet-like form. 00200
- the last compatibility can be transferred to the last. After obtaining the last compatibility that is distributed in the vicinity of the surface opposite to the tomoma, the last
- a method in which a polymer layer is polymerized to form a last polymer layer that is distributed in the vicinity of the surface of the last manno and has a layer structure with the last polymer.
- a polymer composed of a lasting compound containing at least a polymerizable monolastomer on a sheet of a sheet capable of absorbing the polymerizable monomer has a structure in which the cover fill is stacked on the last compatibility.
- the compatibility last adhesion-imparting fat is obtained. After moving to obtain a polymerizability that is distributed in the vicinity of the surface opposite to the last, the polymer is polymerized to the opposite of the last.
- a method characterized by forming a polymer layer that is distributed in the vicinity of the surface and having a layer structure with a polymer layer that is provided with last adhesion.
- a polymerizable material composed of a polymerizable material containing at least a polymerizable monomer, a last, and an adhesion-imparting fat is laminated on the surface of a nomadic sheet capable of absorbing the polymerizable compound, and further covers the compatibility.
- the polymer layer is polymerized to form a polymer layer that is unevenly distributed in the vicinity of the surface opposite to the surface attached to the elastomer. It provides a method characterized in that it has a layer structure with an existing polymer layer.
- the cover fill may have:
- the poly of the existing poly layer is not applied.
- the polymer layer is composed of a monomer and a polymer.
- the polymer of the monomer polymer layer may be an acrylic polymer.
- the component constituting the poly of the monopoly layer may be the same as one of the nomal components constituting the poly of the poly layer on which the last poly is attached.
- an acrylic monomer may be used as the polymerizable monomer.
- the surface of the last side of the last polymer layer is sticky.
- 3 3 is a child microscope true in the aspect of implementation 3.
- the polymer has a layer structure that absorbs at least some kinds of normal components constituting the polymer layer, and the polymer layer is the last monomer for the polymer. It is sometimes referred to as the last-lasting poly-last-poly in the form of being distributed unevenly in the vicinity of the opposite surface). This is the normal state of the distributed part of the last.
- the part that is distributed in the vicinity of the surface opposite to the surface (sometimes referred to as the last or the last), in particular the nature that the last is originally (the, the sex, the flexibility, the adherence to the non-ness, the elasticity (rubber ), Chemical properties such as thermal properties; chemicals such as refractive index; qualities such as air insulation.
- the last poly layer is the opposite of the surface poly layer, and the original nature of such lasts is manifested. This is due to the last last gathering.
- the vicinity of the surface opposite to the surface of the object may be referred to as the surface surface vicinity or the surface vicinity.
- the vicinity of the surface opposite to the surface of the monomer is near the surface of.
- Last polymer layer is the top layer
- the last polymer surface of the light is at least the last polymer distributed in the vicinity of the surface, and at least the polymer of the last polymer layer It may have a layer structure that absorbs various types of components, and the layer structure may be a surface that uses the last poly surface to express the nature of the last.
- the layer structure may be a surface that uses the last poly surface to express the nature of the last.
- it has a layer structure with 0039 last polymer, it is not particularly limited and is selected as necessary, but usually has a sheet-like shape.
- the (lastomer polymer) is adhesive, it can be used as an adhesive or a sheet. therefore
- the side opposite the last poly layer noma and the side of the noma are more sticky and can be double-sided tape or seated if they have a sheet-like shape .
- acrylic rubber-based, acryl-based rubber-based silicone-based, polyester-based poly-ad-based urethane-based fluoric agents, etc. can be used as an adhesive tape or sheet.
- It may be in the form of 0040 or a film. More
- It may have a form wound in a mouth shape, or may have a form in which sheets are stacked.
- the cover film may have or may not have.
- the cover fee may be peeled off or may be configured to maintain the state without being peeled off.
- a normal sheet which is a sheet having an object
- other layers for example, intermediate layers, undercoat layers, etc.
- Last compatibility This is a layer formed by the last compatibility that contains at least a polymerizable monomer that can be polymerized by light or heat.
- Last compatibility Contains at least a polymerizable monomer that can be polymerized by light or heat, or the last.
- it may contain a polymerization initiator, a polymerization initiator, etc.
- Last Coordination Active Energy is polymerized and cured by irradiation with heat or heat to form a poly).
- the last compatible object when it is provided in contact with the last compatible object, the last compatible object
- a polymerizable monomer for example, a radical-compatible monomer such as an acrylic monomer that forms an acrylic polymer; a xy monomer that forms a xy-based fat, or a tan-based monomer that forms an oxtan-based fat
- a radical-compatible monomer such as an acrylic monomer that forms an acrylic polymer
- a xy monomer that forms a xy-based fat or a tan-based monomer that forms an oxtan-based fat
- thione-compatible monoforms such as lute series monoforms that form system fats; combinations with isocyanate polyols that form urethane series fats, and combinations with polyols and polyols that form polystellate series fats.
- acrylic mono Appropriately used.
- the polymerizable monomers may be used alone or in combination.
- the acrylic poly-polyoxy-octane-based fat, the birutel-based fat, the urethane-based fat, the poly-ster-based, each of the acryl-based () -based poly-polyoxy-based poly-poly-octane-based poly It functions as a base polyester based on polyurethane, a base polymer based on urethane, or a polyester based polymer. For this reason, it may contain a last compatible last (sometimes referred to as a lastomer).
- the last polymer layer formed by curing the last compatibility may be the last formed by polymerizing the last.
- the last acrylic material is preferably used as the last. It is preferable that the polymer in the last polymer layer constituting is an acrylic polymer.
- (meth) acrylic steal is preferably used.
- a (meth) acrylate a (meth) acrylic alkyl steal, a (meth) acrylic steal having hydrogen hydride, and a (meth) acrylic steal having an atomic atom can be suitably used.
- the (meth) acrylic alkyl ester one kind may be used, or the above may be combined.
- Such meta) acrylic alkyl esters include, for example, meta) acrylic methyl, meta) acrylic, meta) acrylic fluoro, (meth) acrylic sopropi, (meth) acrylic butel, ) Acrylic (Meth) Acrylic, (Meth) Acrylic Butel Meta) Acrylic Pentel (Meth) Acrylic Pliers, Methacryl Acrylic Sil, Meta) Acrylic
- methacrylic acid examples include chloropentyl (meth) acrylate, cyclosyl (meth) acrylate, isopropyl methacrylate) and the like.
- examples of the (meth) acrylic steal having an oxygen atom include tetrahydrofurfacrylate.
- Examples of (meth) acrylic steal that have (meth) acrylic stealter atoms include (meth) acrylic steal polyalkylene glycols (methacrylates etc.) that have hydrogen fluoride such as methacrylate (methacrylate). Can be mentioned.
- Such (meth) acrylic steal can be used alone or in combination.
- (meth) acrylic steal is used as the main component of the noma that constitutes the last compatibility (Meth) acrylic ester, especially (meth) acrylic alkyl ester with hydrogen hydride, (meth) acrylic ester with methacrylic ester containing elemental atoms
- a copolymerizable monomer may be used as a mono component.
- methacrylic steal constitutes the last compatibility.
- various kinds of polymerizable monomers such as polar monomers and functional monomers may be used, for example, by using a copolymerizable monomer as a monomer component, for example, The viscosity of the polymer layer can be increased, and the polymer of the last polymer layer can be increased, and the copolymer can be used alone or in combination.
- carbon monomers such as methallyl, itaconic malein, maleic acid, croton isocrotonic acid, etc.
- Acid group such as methacrylic, methacrylic, methacrylicyl, methacrylicylalkyl, etc.
- Nlumono is preferably water.
- the dose of 006 mono can depend on the intended use of the resulting product. For example, when it is used in applications that require the wearability of the last polymer layer (for example, the wearability of glass plastic containers), the amount of monomer component
- the dose of a product exceeds 3 with respect to the content of the product, for example, the last polymer layer may become too hard and adhesion may be reduced. If the dose of a polar thing is too small (for example, relative to the amount of the mono component), for example, the cohesion of the last polymer layer may be reduced, resulting in a high strength, and a strong surface. There is a risk that it will be too difficult to handle.
- the polar monomer dose is relative to the amount of the mono component
- ⁇ ⁇ is preferably ⁇ 7.
- aqueous solution may not be sufficient, and there is a risk that quality for use (eg, moisture) will increase.
- quality for use eg, moisture
- the dose of polar things is too small (for example,
- hexanediol di (meth) acrylate J) Tylene glycol dimeth) acrylate, poly) fullerene glycol dimeth) acrylate, neopentyl glycol di (meth) acrylate pentalithitol di (meth) Acrylate, Pentaerythritol J (Meth) Acrylate Pentalythritol Koxa Meta) Acrylate Trityrol Propant J Meta) Acrylate, Tetratyrol Methane J Meta) Acrylate Ali Meta) Acrylate, (Meth) Acrylate, Orange, Polyacrylate, Poly Examples include stear acrylate urethane acrylate and (meth) acrylate (meth) acrylate.
- the dose of the active product can be determined depending on the intended purpose of use. For example, when it is attached to the last polymer layer, it may be used in an application that requires a glass plastic container or the like.
- the monomer component amount is ⁇ ), and preferably ⁇ ⁇ . If the dose of the active substance exceeds the amount of the mono component, for example, may become too high, the last polymer layer may become too hard, and adhesion may be reduced. In addition, if the dose of an active thing is too small (for example, relative to the amount of a mono component), for example, the cohesion of the last polymer layer may decrease and the surface may become too strong to be handled. There is.
- the dose of the multifunctional monomer is 9% of the amount of the mono component.
- polar monomers other than polymerizable monomers include, for example, rusters such as bipropion bi, bi compounds such as ethylene vinyl toluene, fins or ethylene such as ethylene butane isofrene, and isobutylene; Luthenes such as ethers; (meth) acrylic alcohol monoalkylsulphones such as (metha) acryl methoxyl, (meth) yl toloxy, etc.
- Hong monomers such as sodium sulfone; phosphorous monomers such as tilacryloyl sulfo; cyclosyl lei Monomers such as isopropylate; isocyanate monomers such as tacryloyloxyisocyanate; fluorine atom (meth) acrylate silicon atom (meth) acrylate and the like.
- the start of the polymerization may be carried out if necessary. For example, the deviation of the initiation of polymerization or the start of photopolymerization () may be used. In the light of this, the formation of the last polymer layer can utilize the energy reaction using energy lines such as the start of polymerization and the start of photopolymerization (). For this reason, it is possible to maintain the last compatibility and the structure in which the last exists, and it is easy to form a last polymer layer that is distributed in the vicinity of the surface opposite to the surface of the last monomer (near the surface). can do.
- Polymerization initiation is not particularly limited, for example, a nether-tel system Start of polymerization Acetophenone polymerization start, Toll polymerization start, Sulfur chloride polymerization start, Photooxime polymerization start, Benzoin polymerization start Benzyl polymerization start, Benzonone base polymerization start, Ketal base polymerization start, Xanthone base polymerization initiator Etc. can be used. Polymerization start can be used alone or in combination.
- the initiation of ketal polymerization includes, for example, Toxidiphthane 1 on, for example, trade name “Ilchia 6 1 ⁇ Specialty Luz” and the like.
- examples of the initiation of acetophenone-based polymerization include, for example, cyclol, for example, trade name Illkia ( ⁇ Sperty Chemicals, etc., V-toxitophenone, toxiphentophenone, chlorotophenone () tofu, etc.
- examples include benzoin methyl ether, benzoin ether benzoin furter benzoyl ether benzoyl ether, etc.
- As the sphinxide polymerization initiation for example, trade name Lucillin TPO (AS) can be used.
- Examples of the toll-based polymerization start include methylropiophenone 2 tert) femethypropane 1-one.
- Examples of the initiation of sul- yl chloride-based polymerization include 2th-terulene chloride.
- Examples of the oxime polymerization start include full propanedioneoxy) oxy.
- Benzoin-based polymerization starts include, for example, benzoy.
- Examples of benzyl-based polymerization initiation include benzine.
- Benzonone-based polymerization for example, benzonone, benzoy Benzoic acid 3 3 Methyl-oxybenzonone Polybenzonone, cyclosulfur, etc. are included.
- xanthone-based polymerization examples include xanthone, 2-chloroxanthone, methylthioxanthone, methylthioxanthone, isopropylthioxanthone, and ruthioxanthone silthioxanthone.
- the dose for initiating polymerization is not particularly limited.
- it can be selected from the range of ⁇ ⁇ (preferably ⁇ ⁇ 3) for the mono component 1 constituting the last compatibility.
- a chemical reaction by active energy lines may be used.
- active energy is, for example,
- Y neutrons Rays of electrons such as electron beams and ultraviolet rays are listed, and ultraviolet rays are particularly preferable. It should be noted that the duration of irradiation of the active energy line, the irradiation method, and the like are particularly limited as long as the last polymer layer can be formed by curing the last compatibility.
- the start of the system is, for example, thyrothryl, methyl thyrothryl, bismethylpropion) methyl anovalerene valerotril bis (nopropane) chloride, 5-2 yl) propan fluoride, bismethylfuropion Azine) Acid salt, Bis (NN Tylene tyrazine) V Rhodoid peroxide peroxide initiation (benzoyloxy e “ate” etc.) Initiating organic peroxides Nadium compounds; organic peroxides dimethylarine; combinations of phenteraldehyde, allin or kuton, etc.).
- the starting dose is not particularly limited and may be within the range available for starting. If the start of the docking system is set as the start of heat mixing, it is possible to polymerize at room temperature.
- rubber 068 As long as it is a rubber that exhibits rubber properties, it is not particularly limited.
- rubber N graft rubber, isoprene rubber R), butane rubber (), chloroprene rubber (CR) tolyl rubber NR) Tylene rubber (SR), Rubber (1R), Tylene rubber (EPDM, Polyethylene rubber, etc. or Synthetic rubber Terylene Propylene polymer Tylene Propylene polymer, Tylene bipolymer Polyolefin, Chlorinated polyethylene, etc.
- a styrene-based polymer such as a styrene-butylene multiblock polymer (SS), a styrene-ethylene-butylene multiblock polymer (SS), a styrene-ethylene-butylene multi-block polymer (SS), or a styrene-based ethylene multi-block polymer (SS); Polyester Elast Amide Last Urethane Last Ma; Silicone lastoma. The last can be used alone or in combination.
- hydrocarbon last is preferred because of its design range, and in particular, it is possible to select from a wide range of styrene and molecular weight.
- Styrene styrene multi-polymer (SS) Styrene styrene butyl block polymer (S) Styrene styrene Butylene ruttic polymer (SS) Styrene Tylene propylene Ruthiblock polymer (Styrene last such as SS is preferred.
- the last dose in the OO Lastoma polymer layer is: For example, it is possible to select from the range of ⁇ preferably ⁇ 7, and more preferably ⁇ for the components constituting the last compatibility that forms the last polymer layer. . If the amount used exceeds 1, the problem of strength may occur when it becomes difficult or after production. Also, ⁇
- the surface of the last layer of the polymer layer near the surface opposite to the surface of the object will be dispersed in an average manner, and it will be difficult to distribute the lastma, and it may be difficult to express the nature of the last There is.
- the 001 Last Consistency may include nothing if necessary. For example,
- Crosslinks such as ionic silicones such as polyisocyanates, silicones, poxy alkyl-tellurans, etc.) Tackifying Adhesion Aging Oxidation, colorants, materials, etc.) Resin rubber, polyester rubber, natural rubber, etc.).
- carbon flack can be used as a coloring pigment.
- the dose of carbon flack is, for example, the monomer component that constitutes the last compatibility 1
- the last compatibility and the last compatibility containing at least a polymerizable monolast adhesion-imparting fat are preferred.
- the part to which the last part is attached acts as a rubber system (rubber type).
- the original nature of the last may be more manifested.
- adhesion imparting examples include gin rosin conductor fat, polyterpene fat, petroleum fat, umalon / indene fat, styrene fat, phenol fat, xylene fat and the like.
- Last compatibility, mixing and mixing with the above Can be prepared This last compatibility is usually formed into a sheet by laying on the base, etc., so it should have a degree suitable for the work. For example, it can be adjusted by blending a polymer such as acrylic rubber polyurethane or agent, or by combining a last compatible monomer by irradiation of light. Use the desired meter to measure N
- Rotation 1 measured temperature: The degree set by the condition of C is ⁇ a ⁇ , more preferably 1 ⁇ a ⁇ . If the degree is a •, the liquid will flow when the cloth is placed on top, and if it exceeds P a •, the viscosity will be too high and the cloth will be difficult.
- a conventional coater such as a roll coater, die roll coater, gravure roll coater, reverse roll coater, kiss roll coater, dip roll coater, bar coater, knife coater, spray coater, etc.
- Last compatibility is achieved by coating with a coater for the above after having determined the support such as the surface provided by the monomer, the treated surface of the normal cover fill of the monomer sheet.
- the last integrity is formed on both sides of the bright object by the last integrity, and the last integrity last is moved to obtain the last integrity that exists in the vicinity of the surface opposite to the surface of the last mano. It is produced by polymerizing the properties, forming a polymer layer, and obtaining a layer structure with the polymer polymer.
- the mono sheet is not particularly limited as long as it has at least a sheet that can absorb one of the last compatible components, and it is composed of, for example, a monomer. No seat less No seat)
- the monoma sheet is the same as the less sheet.
- Examples of such nomales include sheets such as raft clay Japanese paper) sheets (such as cloth, non-woven fabrics, nets), film poly-acrylic polymers, polyuretan resins, and ethylene bipolymer poxy) rubber rubber. Can be mentioned. Monomer These may be used alone or in combination.
- poly can be suitably used as a material for forming objects. That is, a monomer layer made of a monomer or a polymer can be suitably used, and a sheet having a polymer layer can be suitably used as the monomer sheet.
- a polymer is not particularly limited, but a polymer having at least one compatible monomer as a monomer component is preferred.
- last toma as last toma
- an acrylic polymer is preferable as the polymer forming the thing. This is because the acrylic monomer, which is a polymerizable monomer, easily migrates because the acrylic polymer that forms the acrylic monomer, which is a compatible monomer of the last acrylic polymer, is common.
- it may be composed of a polymer layer obtained by polymerizing a polymer having a similar composition except that the last is removed from the monomer last compatible material.
- it may be composed of () such as mono, acrylic, poxy, octane bilter, urethane and polyester agents.
- an acrylic monomer is used as the polymerizable monomer
- an acrylic polymer having an acrylic polymer having a common constitution as a polymer is preferable from the viewpoint of absorption by the polymerizable monomer.
- the polymerizable product before and after the polymerizable product, it may be constant or may be changed.
- the monomer is a high molecular weight polymer
- a polymer having the same composition is polymerized except that the polymer is removed from the above-mentioned polyacrylic polymer, polyurethane-fat ethylene bipolymer poxy).
- the compatible mono it is usually added by absorbing the compatible mono from the compatible layer. That is, by absorbing the molecularly polymerizable substance that forms a thing.
- it may be a monomer whose volume increases by absorbing a monomer or a polymerizable monomer.
- 0089 is a molecular layer, for example,
- the treated surface of the cover fill
- the molecular material is applied by the above coater.
- the molecular layer provided on the support may be dried and / or cured (for example, by light) as necessary.
- it is adjusted to a suitable degree by combining a polymer such as an acrylic rubber agent or partially combining a polymerizable monomer by heating light irradiation when being coated on the above-mentioned molecular support. Moyo.
- the value before absorption of the 0090 monomer can be selected from the range of ⁇ J, preferably ⁇ / u, more preferably ⁇ ). Further, it may have a mono-single layer or a stacked state.
- the mono sheet When the mono sheet is a non-sheet, it can be used for paper such as paper, non-woven metal plates, etc.
- a plastic body such as a sheet; a rubber system such as a sheet; a sheet such as a plastic film of a plastic system and other groups (or a body of a sheeter or the like) can be used.
- a plastic sheet such as a plastic fill sheet can be suitably used as a material for such a plastic sheet, for example, polyethylene (PE), polyfluorene (PP), ethylene-fluorene polymer, and ethylene-bipolymer EVA.
- activation energy lines it is preferable to use those that do not obstruct the activation energy lines.
- corona treatment, chrome treatment, ozone exposure, flame exposure, high piezoelectric exposure, and ion physics can be applied to improve adhesion to objects.
- it may be coated with silicon).
- the substrate is easily peeled off from the mono layer.
- the surface can be raised. Like this, mono
- 0095 can be selected according to the strength, flexibility, and purpose of use. For example, it is generally OO to OOJ), preferably 1 to 3 and more preferably 3 to 34 degrees. Not limited. It may have a single layer or a stacked state.
- the last compatibility is established on one side of the object using the elastomeric properties, and after obtaining the last properties, the last properties are overlapped to form the last polymer layer.
- the reaction is adversely affected by in the air. Therefore, it is preferable to cover the surface of the polymer with a cover fill.
- a cover fill When using, even if you remove the cover fill You can use it without removing the cover fill. If the cover fill is used without removing the cover fill, the cover fill is used as a part of the cover.
- the 0097 cover fill is not particularly limited even if it is difficult to contain oxygen, but a transparent one is preferred when using photopolymerization.
- a cover fill for example, paper for use can be used.
- the cover fill has () on at least one side, for example, m), for example, polytetrafluoroethylene, polychlorotrifluoroethylene, polyfluorini, polyfluoridene, tetrafluoro.
- adhesion material composed of a thylene / xafluorofluorene polymer (chlorofluorene / vinylidene polymerization) or an apolar polymer (adhesive material composed of a fin-based fat such as polyethylene or polyfluorene).
- chlorofluorene / vinylidene polymerization chlorofluorene / vinylidene polymerization
- apolar polymer adhesive material composed of a fin-based fat such as polyethylene or polyfluorene
- cover film for example, a cover film (having a cover film) formed on the other side of the cover film may be used, or a cover film may be left as it is.
- cover films include plastic films (polyethylene terephthalate film, etc.), olefin films, polyterylene film, polypropylene film, etc., polyvinyl films, poly films, poly films (nylon films), Yon fill, and other plastics. System film)
- the cover film is a light plastic film (especially polyethylene terephthalate film). Can be suitably used. 00 is not particularly limited, for example, silicone
- Fluoroalkyl-based agents can be used. They may be used alone or in combination. Note that the cover fill that has been treated by is formed by, for example, the following method.
- cover fill is not particularly limited, it can be selected from the range of, for example, ⁇ 1 or ⁇ ) from the viewpoint of ease of handling and economy.
- the cover fill may have a single layer or a stacked state.
- At least one of the components constituting the polymer polymer layer can be absorbed.
- elastomer polymer layer is the top layer
- the last polymer polymer layer is provided on the top of the nozzle, so the last polymer polymer layer is last. For this reason, the elastomer polymer layer is the best. It exhibits the original nature of the last layer.
- the last compatibility is provided by moving the last structure.
- the last compatibility After obtaining the last compatibility containing the elastomer in a form that is distributed unevenly in the vicinity of the surface opposite to the surface and the surface near the surface, the last compatibility is polymerized to form the last polymer layer, and the last polymer layer It can be manufactured by obtaining a layer structure.
- the last compatibility consisting of a last compatible material containing at least a polymerizable mono last is laminated on the surface of the non-sheet that can absorb the polymerizable mono (the surface of the mono sheet), and further the last compatibility.
- the cover film is laminated on the top, and the last layer is moved so that it is biased near the surface of the layer surface on the cover film side (near the surface opposite to the surface of the object).
- the last compatibility is polymerized by light irradiation and heating, and the vicinity of the surface of the layer on the cover film side (opposite to the surface with the object) of
- a polymerizable monomer, a last, an adhesion-imparting fat are applied to both sides of the monomer capable of absorbing the polymerizable monomer.
- the synthetic last fat was moved, and polymerizability distributed in the vicinity of the surface opposite to the last attachment was obtained.
- a poly layer is formed which is distributed in the vicinity of the surface opposite to the surface where the elastomer is applied, and a layer structure with the layer where the elastomer is applied is obtained. It can also be produced using the method produced by the above method.
- a polymerizable layer composed of a polymerizable substance containing at least a polymerizable monomer, a last, and an adhesion resin, and a cover film is laminated on the composition. After the last adhesion-imparting fat is moved to obtain the polymerizability that is distributed in the vicinity of the opposite surface to the last adhesion-giving area, the compatibility is polymerized and the last adhesion-giving nose is obtained.
- the constant light irradiation may be manufactured by (constant production, () the constant light irradiation.
- a photopolymerizable composition containing a last (sometimes referred to as “lastomer polymerizability”) on a covered film on which at least one surface has been separated, G.
- last sometimes referred to as “lastomer polymerizability”
- Examples of 011 irradiation include irradiation of external rays with a flak light lamp chemical run, a high-pressure mercury-free metal run lamp, and the like.
- examples of the heating include the following (for example, a heating method using an electric heater, a heating method using an infrared ray, etc.).
- a specific film having a form formed by a cover film having a last polymerizable surface provided with a last polymerizable surface provided on a sheet of a cover film It may be manufactured by irradiating with a monomer.
- 011 is the length from the last contact with the last match to the end of the match.
- the polymerization initiation can be easily controlled by light irradiation, it is preferable to irradiate with light above contact, preferably above, and more preferably within 1 minute.
- the last poly layer at 0 it is distributed in the vicinity of the surface of the last toma surface (near the surface opposite to the surface of the object).
- the layer structure consisting of the layer of the polymer and the layer of the polymer (of the last part of the layer structure) is (preferably lower than the lower). This is because, when it is provided in contact with the last polymer forming the last polymer layer, one monomer component is absorbed by the monomer, and the last polymer is polymerized.
- the last polymer layer can be controlled by adjusting the amount of the last polymer layer in the direction from the surface, so that the last polymer layer can be controlled by adjusting the last dose. Can control the nature of the nature of
- 0119 is not particularly limited, it is usually 1 to U or more from the point of handling and cost. Preference is 3 to U.
- the layer structure consisting of mono layer and last polymer layer may be referred to as a layer structure, but it is usually limited to 1 to better than OO. Is ⁇ 5 U).
- a body length of 4 may cause problems in the case of Cotin's, especially when it has a sheet-like form.
- the last polymer layer where the last polymer layer last is distributed, the last polymer layer is mixed with the last polymer layer.
- the part where the last is distributed (last)
- the part where the last is not distributed may be called the presence of the last, because it has a last-like state.
- the presence of the last layer of the poly layer (sometimes referred to as “up”, “preferably”, “preferably” is “up”). This is because it may be difficult to exhibit the original properties.
- the thickness of the last poly layer in, although not particularly limited, is preferably such that it has the above-mentioned ratio.
- the physical thickness is, for example, 1 to (preferably 5 to O, more preferably 5).
- the extent to which the last property of the last polymer can be controlled.
- the last polymer layer is the last dispersed polymer layer by comparing the elastomer polylast dispersion polymer (polyester in which the last is dispersed in the thickness direction) with a common content of 026 and the last component. Compared to, it demonstrates the original nature of the last.
- the Last Polymer Layer is a small amount that does not reveal the original nature of the Last in the Last Dispersion Polymer Layer. Exhibits the inherent nature of the last in a large amount. This is because the last polymer layer has a layered last in which the last is gathered.
- the last polymer and the last polymer have surfaces that have the properties of the last surface and the polymer surface. For this reason, using For the purposes of joining articles made of the same quality, for example, as a last, a tyrene-based last-methylene-based last attachment (rubber-based) is used as a polymer, and an acrylic-based polymer (acrylic) is used as a material such as a flash and a material such as a metal Applications that require flexibility on the other side and applications that require resistance on the other side Applications that require adherence on one side and applications that require flexibility on the other side require hydrophilicity on the other side It can be used for applications in which the other side requires properties, heat resistance is required in the other side, and heat meltability is required in the other side.
- a product having a last polymer layer can be produced without leaving (for example, having an adverse effect on the boundary between the agent and the organic compound).
- the ratio of the monomer is not particularly limited because it is not particularly limited as long as it can absorb one of the polymerizable monomers used in the last compatibility. In other words, as long as it can absorb any of the polymerizable monomers used in lasting compatibility, it is free of adhesives, polymer layers, etc., as well as plastic sheets, card coats, colored layers, etc. Any of these can be present. For this reason, it is possible to manufacture on the surface of such as an adhesive poly layer and a plastic sheet coated color layer which are not restricted to the sheet.
- the gel rate is not particularly limited. Therefore, in the monomer polymer layer, the gel:) can be obtained even if the gel rate is reduced to a small extent or almost not. For this reason, if a poly layer having a high (high gel ratio) is used,
- the thermal properties In the poly layer, the thermal properties and can be exhibited.
- Mono acrylate, acrylate, acrylic :, photopolymerization initiation Product name Ilkia 1 ⁇ Specialty Kecals), Heavy platform (Product name Illukia 84 ⁇ Specialty Luz)
- Styrene / ethylene / ethylene block polymer (SES product name: RATON G clayton polymer zipan).
- Xanthdiol diacrylate was added as follows to obtain the last polymer compatibility (sometimes referred to as the last compatibility D).
- last compatibility (sometimes referred to as lastomer compatibility (E)).
- a 38-thickness polyethylene terephthalate film (product name: RN 8 Ryoh Chemical Polyster Film) with one side treated with silicone was used.
- a polyethylene terephthalate film with a thickness of one side treated with a silicone system (product name R Ryo Chemical Polyester Film) was used.
- the sheet A) is sometimes referred to.
- the last compatibility corresponding to the following, the noma layer and the last after fabrication A sheet having a laser compatibility was produced on the cover film by spreading so that the degree of polymerization was about 8 4.
- the sheet having the last compatibility was laminated on the cover sheet (A), which was formed by peeling off the cover fill and contacting with the monolast compatibility.
- ultraviolet rays (: W 2) are simultaneously irradiated from the surface by using a Brautleytran to cure the lasting compatibility and form the lasting polymerization (last polymerization). This was made.
- Fabrication was carried out in the same manner as in the practice, except that the last polymerization after the partial production was made so that the degree of last polymerization was as high as possible, the film was used in place of the noma sheet (A).
- the film was peeled off and the 8 urn thick polyethylene terephthalate film product name Lumirror S) was combined with: O and length: to obtain a measurement sample. 2. Remove the cover fill from the sun-flux to expose the last polymerized surface. C. Propylene coated PP) Stainless steel (US). After 3 aging with C. Using a tensile tester (product name: TCM N Minebea) in an atmosphere of C, tension 3 O
- the cover fill was peeled off and a 38-thickness polyethylene terephthalate film (product name: Lumira S) was put together and cut into O length: to obtain a measurement sample.
- a 38-thickness polyethylene terephthalate film product name: Lumira S
- the surface is brought out and crimped under the conditions of C-enclosed propylene (P) and stainless steel (US). Jinged with C.
- the cover fill was peeled off and the polymer was polymerized to obtain a measurement sample. And the last of Sanfuru
- each cover with the cover fill removed was observed with a microscope (SM).
- SM scanning microscope
- S34N manufactured by Hitachi Technologies, Ltd. was used.
- S The submicroscope
- a means last polymerization, and means last polymerization last.
- the sheet (of the film monolayer and the cover fill) was measured, and the thickness of the cover cover film was subtracted from the thickness of the sheet.
- the length of the last polymerization last is an average value determined from the true value of the child microscope of the surface by the scanning microscope.
- the last polymerization was calculated from the following.
- Last in the layer structure (: A total) with last-no-polymerization.
- the ratio of occupying was calculated from the following.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Toxicology (AREA)
- General Chemical & Material Sciences (AREA)
- Laminated Bodies (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Adhesive Tapes (AREA)
- Graft Or Block Polymers (AREA)
Abstract
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US12/734,823 US8501306B2 (en) | 2007-11-30 | 2008-11-11 | Viscoelastic articles with polymer layer containing elastomer unevenly distributed |
EP08853852.5A EP2226191A4 (en) | 2007-11-30 | 2008-11-11 | VISCOELASTIC LINK WITH A POLYMER LAYER CONTAINING A ELASTOMER ARRANGED THEREIN |
CN200880118447.1A CN102405137B (zh) | 2007-11-30 | 2008-11-11 | 具有弹性体不均匀存在的聚合物层的粘弹性部件 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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JP2007-309987 | 2007-11-30 | ||
JP2007309987A JP4628416B2 (ja) | 2007-11-30 | 2007-11-30 | エラストマー偏在ポリマー層を有する粘弾性部材 |
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WO2009069485A1 true WO2009069485A1 (ja) | 2009-06-04 |
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PCT/JP2008/070832 WO2009069485A1 (ja) | 2007-11-30 | 2008-11-11 | エラストマー偏在ポリマー層を有する粘弾性部材 |
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US (1) | US8501306B2 (ja) |
EP (1) | EP2226191A4 (ja) |
JP (1) | JP4628416B2 (ja) |
KR (1) | KR20100089863A (ja) |
CN (1) | CN102405137B (ja) |
WO (1) | WO2009069485A1 (ja) |
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US20120058329A1 (en) * | 2008-11-28 | 2012-03-08 | Sakurai Aizoh | pressure sensitive adhesive composition and a pressure sensitive adhesive tape |
US20120328800A1 (en) * | 2010-02-26 | 2012-12-27 | Sung Soo Yoon | PRESSURE SENSITIVE ADHESIVE COMPOSITION (As Amended) |
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US8356373B2 (en) | 2009-03-06 | 2013-01-22 | Noel Group Llc | Unitary composite/hybrid cushioning structure(s) and profile(s) comprised of a thermoplastic foam(s) and a thermoset material(s) |
USD693145S1 (en) | 2010-03-03 | 2013-11-12 | Noel Group Llc | Mattress bed cushion |
USD694553S1 (en) | 2010-03-03 | 2013-12-03 | Noel Group Llc | Mattress bed cushion |
USD688492S1 (en) | 2010-03-03 | 2013-08-27 | Noel Group Llc | Mattress bed cushion |
USD693144S1 (en) | 2010-03-03 | 2013-11-12 | Noel Group Llc | Mattress bed cushion |
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- 2008-11-11 KR KR1020107011715A patent/KR20100089863A/ko not_active Application Discontinuation
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Also Published As
Publication number | Publication date |
---|---|
JP2009132038A (ja) | 2009-06-18 |
CN102405137A (zh) | 2012-04-04 |
CN102405137B (zh) | 2014-09-03 |
KR20100089863A (ko) | 2010-08-12 |
US20100304104A1 (en) | 2010-12-02 |
EP2226191A1 (en) | 2010-09-08 |
JP4628416B2 (ja) | 2011-02-09 |
EP2226191A4 (en) | 2014-08-27 |
US8501306B2 (en) | 2013-08-06 |
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