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WO2019049793A1 - Feuille stratifiée - Google Patents

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Publication number
WO2019049793A1
WO2019049793A1 PCT/JP2018/032430 JP2018032430W WO2019049793A1 WO 2019049793 A1 WO2019049793 A1 WO 2019049793A1 JP 2018032430 W JP2018032430 W JP 2018032430W WO 2019049793 A1 WO2019049793 A1 WO 2019049793A1
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WO
WIPO (PCT)
Prior art keywords
laminated
less
sheet
layer
mass
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/JP2018/032430
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English (en)
Japanese (ja)
Inventor
義朗 小田
智之 菱田
淳人 田所
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kao Corp
Original Assignee
Kao Corp
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Filing date
Publication date
Application filed by Kao Corp filed Critical Kao Corp
Publication of WO2019049793A1 publication Critical patent/WO2019049793A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/36—Layered products comprising a layer of synthetic resin comprising polyesters
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/18—Manufacture of films or sheets
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/04—Oxygen-containing compounds
    • C08K5/10—Esters; Ether-esters
    • C08K5/11—Esters; Ether-esters of acyclic polycarboxylic acids
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K7/00—Use of ingredients characterised by shape
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L21/00—Compositions of unspecified rubbers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L53/00—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
    • C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
    • C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
    • C08L67/03—Polyesters derived from dicarboxylic acids and dihydroxy compounds the dicarboxylic acids and dihydroxy compounds having the carboxyl- and the hydroxy groups directly linked to aromatic rings
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16F—SPRINGS; SHOCK-ABSORBERS; MEANS FOR DAMPING VIBRATION
    • F16F15/00—Suppression of vibrations in systems; Means or arrangements for avoiding or reducing out-of-balance forces, e.g. due to motion
    • F16F15/02—Suppression of vibrations of non-rotating, e.g. reciprocating systems; Suppression of vibrations of rotating systems by use of members not moving with the rotating systems

Definitions

  • the present invention relates to a laminated sheet for a damping material.
  • FIG. 1 is a schematic view showing the cross-sectional structure of various aspects of the laminated sheet of the present invention.
  • FIG. 2 is a schematic diagram which shows the cross-section of the various aspect of the lamination sheet as comparison object.
  • FIG. 3 is a schematic diagram which shows the cross-section of the one aspect
  • the present invention relates to a laminated sheet having sufficient rigidity and impact strength to an extent that metal material is unnecessary, and having excellent vibration damping properties.
  • the laminated sheet of the present invention has sufficient rigidity and impact strength to such an extent that a metal material is unnecessary, and can exhibit excellent vibration damping properties.
  • the laminated sheet of the present invention is a laminated sheet having a laminated structure in which the first damping layer is laminated on the upper surface of the polycarbonate layer and the second damping layer is laminated on the lower surface of the polycarbonate layer, Component (B) which is a thermoplastic polyester resin (A) composed of a component including a dicarboxylic acid component and a diol component, the first damping layer and the second damping layer, a plasticizer and / or an elastomer, And a sheet-like molded article of a polyester resin composition comprising the inorganic filler (C).
  • Component (B) which is a thermoplastic polyester resin (A) composed of a component including a dicarboxylic acid component and a diol component, the first damping layer and the second damping layer, a plasticizer and / or an elastomer, And a sheet-like molded article of a polyester resin composition comprising the inorganic filler (C).
  • FIG. 1A The cross-sectional structure of one aspect of the laminated sheet of the present invention having such a laminated structure as a basic skeleton is schematically shown as FIG. 1A.
  • the first damping layer 2 is laminated on the upper surface of the polycarbonate layer 1
  • the second damping layer 3 is laminated on the lower surface of the polycarbonate layer 1.
  • the direction in which the first damping layer 2 is stacked as viewed from the polycarbonate layer 1 of the laminated sheet shown in FIG. 1A is referred to as “upper” or “upper surface”
  • the second damping layer 3 is The direction in which the layers are stacked is referred to as "lower” or "lower surface”.
  • the present invention is characterized in the position where the damping layer is present.
  • vibration control is performed with a two-layer structure in which the damping material is simply attached to the sheet serving as a base (made of polycarbonate or the like) having self-supporting properties. It is conceivable to have a three-layer structure sandwiching the material.
  • a sheet having a two-layer structure in which a damping material is simply attached to a sheet serving as a base material can provide high damping properties, it is not sufficient in terms of strength and heat resistance.
  • the mechanism by which the laminated sheet of the present invention exerts an excellent damping effect is presumed as follows. That is, by arranging the damping layer on the surface (that is, both the upper surface and the lower surface) of the laminated sheet, when distortion such as bending is applied to the sheet, the strain energy is biased to the surface-side damping layer. As a result, energy loss occurs, and it is considered that damping property is developed.
  • the laminated sheet of the present invention Since the laminated sheet of the present invention has rigidity, impact strength and excellent vibration damping properties, it can be used as a speaker, television, radio cassette player, headphone, audio component, microphone, etc. as a material for an audio equipment case; Parts and housing materials as electric drills, electric tools such as electric screwdrivers, computers, projectors, servers, electric products with cooling fans such as POS systems, washing machines, clothes dryers, air conditioner indoor machines, sewing machines, dish washing Machines, fan heaters, complex machines, printers, scanners, hard disk drives, video cameras, etc .; parts of electric products with vibration source and housings as electric toothbrushes, electric shavers, massage machines etc .; Parts and housing materials for generators, gas generators, etc .; Parts and housing materials for refrigerators, vending machines, outdoor units of air conditioners, dehumidifiers, household generators; materials for automobile parts such as dashboards, instrument panels, floors, doors, roofs, etc.
  • Materials for engines such as oil pans, front covers, lockers, etc .; interior materials for floors, walls, side plates, ceilings, doors, chairs, tables, etc., as housing materials for railway parts, casings and parts around motors, Various protective covers, etc .; Materials for airplane parts, such as interior materials such as floors, walls, side plates, ceilings, chairs, and tables, casings and parts around engines, etc. Cases for engine room as materials for marine parts Wall materials, enclosures and wall materials for measurement rooms; Walls, ceilings, floors, partition boards, soundproof walls, shutters, curtain rails, piping ducts, stairs, doors, etc.
  • kerosene cans, drums can be used in the composite container, tank trucks, shipping cases and the like.
  • the layer configuration of the laminated sheet of the present invention will be described.
  • the thickness (ie, total thickness) of the entire laminated sheet of the present invention is preferably 0.3 mm or more, more preferably 1.0 mm or more, still more preferably 1. 5 mm or more, more preferably 2.0 mm or more, still more preferably 2.5 mm or more, preferably 30 mm or less, more preferably 10 mm or less, still more preferably from the viewpoint of mass, strength and rigidity required for use It is 5.0 mm or less.
  • a polycarbonate layer is a sheet-like molded object shape
  • the polycarbonate layer is not limited to a single layer, but may be a layer composed of a plurality of layers (for example, a layer formed by thermocompression pressing of a plurality of polycarbonate layers) or a single polycarbonate layer. Treat as. The same applies to the first damping layer and the second damping layer.
  • the thickness of the polycarbonate layer is preferably 0.05 mm or more, more preferably 0.10 mm or more, still more preferably 0.15 mm or more from the viewpoint of the characteristics of the molding method for producing the thin sheet to be used. From the viewpoint of the characteristics of the molding method for producing an object plate, it is preferably 10 mm or less, more preferably 5.0 mm or less, and still more preferably 1.0 mm or less.
  • their thicknesses may be the same or different.
  • the thicknesses of the polycarbonate layer 1, the polycarbonate layer 4 and the polycarbonate layer 5 shown in FIG. 1D may be the same or different.
  • the first vibration damping layer is a sheet-like molded article of a polyester resin composition containing the component (A), the component (B) and the component (C) described later.
  • the thickness of the first damping layer is preferably 0.05 mm or more, more preferably 0.2 mm or more, and still more preferably 0.4 mm or more from the viewpoint of the characteristics of the molding method for producing the thin sheet to be used. From the viewpoint of the characteristics of the molding method for producing the thick plate to be used, the thickness is preferably 10 mm or less, more preferably 5.0 mm or less, and still more preferably 1.0 mm or less.
  • a polycarbonate layer may be further laminated on the upper surface of the first damping layer.
  • the cross-sectional structure of one aspect of the laminated sheet of the present invention having such a structure is schematically shown as FIG. 1B.
  • the first damping layer 2 is laminated on the upper surface of the polycarbonate layer 1
  • the polycarbonate layer 4 is further laminated on the upper surface of the first damping layer 2.
  • the second damping layer 3 is stacked.
  • the thickness of the polycarbonate layer laminated on the upper surface of the first damping layer is preferably 0.05 mm or more, more preferably 0.10 mm or more, and further preferably from the viewpoint of the characteristics of the molding method for producing the thin sheet to be used.
  • the thickness is preferably 0.15 mm or more, and preferably 10 mm or less, more preferably 5.0 mm or less, and still more preferably 1.0 mm or less from the viewpoint of the characteristics of the molding method for producing the thick plate to be used.
  • the thickness of the polycarbonate layer laminated on the upper surface of the first damping layer is preferably 200% or less, more preferably 200% or less, from the viewpoint of the damping effect, when the thickness of the first damping layer is 100%. Is 100% or less, more preferably thinner than the thickness of the first damping layer, specifically 70% or less, preferably 10% or more, more preferably from the viewpoint of improving rigidity and impact strength. Is 20% or more.
  • the second damping layer is a sheet-like molded product of a polyester resin composition containing the component (A), the component (B) and the component (C) described later.
  • the thickness of the second damping layer is preferably 0.05 mm or more, more preferably 0.1 mm or more, still more preferably 0.2 mm or more, from the viewpoint of the characteristics of the molding method for producing the thin sheet to be used. From the viewpoint of the characteristics of the molding method for producing the thick plate to be used, the thickness is preferably 10 mm or less, more preferably 5.0 mm or less, and still more preferably 1.0 mm or less.
  • the thickness of the second damping layer may be the same as or different from the thickness of the first damping layer.
  • a polycarbonate layer may be further laminated on the lower surface of the second damping layer.
  • the cross-sectional structure of one aspect of the laminated sheet of the present invention having such a structure is schematically shown as FIG. 1C.
  • the first damping layer 2 is laminated on the upper surface of the polycarbonate layer 1
  • the second damping layer 3 is laminated on the lower surface of the polycarbonate layer 1
  • the second damping layer is further formed.
  • the polycarbonate layer 5 is laminated on the lower surface of the third layer 3.
  • the thickness of the polycarbonate layer laminated on the lower surface of the second damping layer is preferably 0.05 mm or more, more preferably 0.15 mm or more, and further preferably from the viewpoint of the characteristics of the molding method for producing the thin sheet to be used.
  • the thickness is preferably 0.20 mm or more, and preferably 10 mm or less, more preferably 5.0 mm or less, and still more preferably 1.0 mm or less from the viewpoint of the characteristics of the molding method for producing the thick plate to be used.
  • the thickness of the polycarbonate layer laminated on the lower surface of the second damping layer is preferably 200% or less, more preferably 200% or less, from the viewpoint of the damping effect, when the thickness of the second damping layer is 100%. Is 100% or less, more preferably thinner than the thickness of the second damping layer, specifically 70% or less, preferably 10% or more, more preferably from the viewpoint of improving rigidity and impact strength. Is 20% or more.
  • FIG. 1D As a further aspect of the laminated sheet of the present invention, an aspect in which the cross-sectional structure is schematically shown as FIG. 1D can be mentioned.
  • a polycarbonate layer 4 or a polycarbonate layer 5 is further laminated on the upper surface of the first damping layer 2 and the lower surface of the second damping layer 3, respectively.
  • the thickness of the polycarbonate layer 5 may be the same as or different from the thickness of the polycarbonate layer 4.
  • FIG. 3A As a further aspect of the laminated sheet of the present invention, an aspect in which the cross-sectional structure is schematically shown as FIG. 3A can be mentioned.
  • the laminated sheet shown in FIG. 3A has a structure in which a damping layer 6 is further laminated on the upper surface of the polycarbonate layer 4 of the laminated sheet shown in FIG. 1B.
  • the thickness of the damping layer 6 may be the same as or different from the thickness of the polycarbonate layer 4.
  • the laminated sheet of the present invention is compatible with the rigidity and impact strength of the laminated sheet and the damping property.
  • the total thickness of the polycarbonate layer and the total thickness of the damping layer depend on the situation where the laminated sheet is applied, that is, the scene where importance is placed on rigidity and impact strength, or where the damping property of the laminated sheet is emphasized.
  • the preferred relationship with can vary.
  • the total thickness of the polycarbonate layer means the thickness of the polycarbonate layer sandwiched between the first and second damping layers, and the top surface of the first damping layer (if any) and / or the second Of the thickness of the polycarbonate layer laminated on the lower surface of the damping layer, and the total thickness of the damping layer means the thickness of the first damping layer and the thickness of the second damping layer And the thickness of the additional damping layer).
  • the total thickness of the polycarbonate layer is preferably equal to or greater than the total thickness of the damping layer.
  • the total thickness of the damping layer is 100%
  • the total thickness of the polycarbonate layer is preferably 100% or more, more preferably 200% or more, still more preferably 300% or more, and the upper limit is preferably 2000% or less, more preferably Is less than 1000%.
  • the total thickness of the polycarbonate layer is preferably equal to or less than the total thickness of the damping layer.
  • the total thickness of the damping layer is 100 When it is%, the total thickness of the polycarbonate layer is preferably 100% or less, more preferably 67% or less, and the lower limit is preferably 33% or more.
  • the surface presence amount of the elastomer in the damping layer constituting the laminated sheet of the present invention, that is, the sheet-like molded product of the polyester resin composition is preferably 0.5% or more, more preferably from the viewpoint of adhesiveness with the PC sheet. Is preferably 1% or more, more preferably 5% or more, and from the viewpoint of maintaining the elastic modulus, preferably 50% or less, more preferably 40% or less, still more preferably 30% or less.
  • the surface existing amount of the elastomer is determined by immersing the sheet-like molded product of the polyester resin composition in a solvent to remove the elastomer, and observing the molded product after treatment with an SEM. Specifically, the surface abundance of the elastomer is indicated by the area% of the void portion per fixed area, where the void portion of the molded article after the treatment is a region where the elastomer was present.
  • the particle diameter of the elastomer in the damping layer constituting the laminated sheet of the present invention is preferably 0.01 ⁇ m or more, more preferably 0.05 ⁇ m or more, still more preferably 0.1 ⁇ m or more from the viewpoint of adhesion to the PC sheet On the other hand, in view of maintaining the elastic modulus, it is preferably 100 ⁇ m or less, more preferably 70 ⁇ m or less, and still more preferably 50 ⁇ m or less.
  • the particle size of the elastomer is determined by observing the molded body after removal of the elastomer, which is obtained by the same method as the method for determining the "surface amount of the elastomer" described above, by SEM.
  • each void is measured, with the void portion of the molded body as the area where the elastomer was present.
  • the diameter of a total of 100 holes is measured, and the average value is taken as the particle size of the elastomer.
  • the damping layer constituting the laminated sheet of the present invention preferably has a large surface area from the viewpoint of adhesion to polycarbonate.
  • the large surface area means that the "surface area / area of arbitrarily designated area” is large.
  • the “surface area / area of arbitrarily designated area” is preferably 1 or more, more preferably 2 or more, still more preferably 5 or more, still more preferably 8 or more, while the sheet shape Preferably, it is 100 or less, more preferably 50 or less from the viewpoint of the stability of
  • the “surface area / area of arbitrarily designated area” can be measured using a three-dimensional image obtained by a confocal laser microscope.
  • the polycarbonate used for the polycarbonate layer has a structure containing a carbonic acid ester bond in the main chain of the molecule, ie,-(O-R-OCO)-(where R is an aliphatic group, an aromatic group)
  • R is an aliphatic group, an aromatic group
  • the lamination sheet which has the self-supporting property in which the metal plate for holding a shape is unnecessary can be obtained.
  • polycarbonate copolymerized with a specific monomer is more preferable.
  • the melt flow rate (MFR) of the polycarbonate used in the polycarbonate layer is preferably 0.1 g / 10 min or more, more preferably 0.1 g / 10 min or more, under the conditions of 300 ° C. and 1.2 kgf, from the viewpoint of extrusion molding and extruder characteristics.
  • 0.5 g / 10 min or more, more preferably 1.0 g / 10 min or more, preferably 20 g / 10 min or less, more preferably 15 g / 10 min or less, from the viewpoint of heat press formability Is less than 8.0 g / 10 min.
  • the MFR value of polycarbonate is measured by the method described in the examples below.
  • the polycarbonate resin composition in the present invention may contain various additives such as a general ultraviolet light absorber, a heat stabilizer, a colorant, a release agent, a lubricant, an antistatic agent and the like.
  • the compositions of the resin compositions constituting them may be the same or different.
  • the composition of the resin composition constituting the polycarbonate layer 1 shown in FIG. 1D, the composition of the resin composition constituting the polycarbonate layer 4 and the composition of the resin composition constituting the polycarbonate layer 5 may be identical to each other. , May be different.
  • the polyester resin composition used for the first damping layer and the second damping layer in the present invention is a thermoplastic polyester resin (A) composed of a dicarboxylic acid component and a diol component, a plasticizer / or an elastomer. It contains a component (B) as well as an inorganic filler (C).
  • the composition of the polyester resin composition that constitutes the first damping layer may be the same as or different from the composition of the polyester resin composition that constitutes the second damping layer.
  • the elastic modulus of the entire resin composition is improved while the loss factor is decreased.
  • the reduction of the loss factor is due to the reduction of the amount of energy loss in the resin portion because the proportion of the resin in the resin composition is reduced by the addition of the filler. Therefore, in the present invention, by adding a plasticizer and / or an elastomer to such a system, by imparting flexibility and facilitating energy loss, the loss coefficient is improved and the elastic modulus of the resin composition is increased. While reducing the loss factor.
  • friction occurs at the interface between the resin or the plasticizer and / or the elastomer and the inorganic filler to cause energy loss, which further suppresses the loss factor reduction. It is estimated that
  • the upper limit of the mass average molecular weight of the thermoplastic polyester resin (A) in the present invention is preferably 300,000.
  • the upper limit does not change depending on the type of thermoplastic polyester resin (A) used, but from the viewpoint of improving the loss coefficient, as the lower limit, for example, polybutylene terephthalate resin is used as the thermoplastic polyester resin (A)
  • 70,000 or more is preferable, 80,000 or more is more preferable, and 100,000 or more is still more preferable.
  • polytrimethylene terephthalate resin as a thermoplastic polyester resin (A)
  • 60,000 or more is preferable and 70,000 or more is more preferable.
  • thermoplastic polyester resin (A) When using a polyethylene terephthalate resin as a thermoplastic polyester resin (A), 30,000 or more is preferable, 40,000 or more is more preferable, 50,000 or more is still more preferable.
  • the polyester resin composition in this invention has the absolute crystallinity degree mentioned later, a minimum changes with values of absolute crystallinity degree (Xc), and if absolute crystallinity degree is 5% or more and 37% or less, Even if the mass average molecular weight of the thermoplastic polyester resin (A) used is less than 50,000, performance can be exhibited, and, for example, 20,000 or more can be mentioned.
  • the mass average molecular weight of the thermoplastic polyester resin (A) to be used is preferably 50,000 or more.
  • the mass average molecular weight of the thermoplastic polyester resin (A) can be measured according to the method described in the examples described later.
  • the lower limit of the absolute crystallinity degree (Xc) of the polyester resin composition in the present invention may be preferably 5%, but it is as follows according to the type of thermoplastic polyester resin (A) used from the viewpoint of improving the loss coefficient. Range is indicated. For example, when using a polybutylene terephthalate resin as the thermoplastic polyester resin (A), 10% or more is preferable, 15% or more is more preferable, 20% or more is more preferable, 25% or more is more preferable, 35% or less is preferable 30% or less is more preferable, and 28% or less is still more preferable.
  • thermoplastic polyester resin (A) When using polytrimethylene terephthalate resin as a thermoplastic polyester resin (A), 10% or more is preferable, 15% or more is more preferable, 20% or more is still more preferable, and 35% or less is preferable. When using a polyethylene terephthalate resin as the thermoplastic polyester resin (A), 10% or more is preferable, 15% or more is more preferable, 20% or more is more preferable, 25% or more is more preferable, and 35% or less is preferable. In addition, since the thermoplastic polyester resin (A) in the present invention has the above-described mass average molecular weight, the value of the absolute crystallinity degree varies depending on the value of the mass average molecular weight of the resin (A).
  • the mass average molecular weight of the resin (A) is 50,000 or more and 150,000 or less, the performance can be exhibited even in the case of more than 37%, and for example, preferably 40% or less as the upper limit.
  • the mass average molecular weight is less than 50,000, it is preferably 37% or less.
  • the absolute crystallinity degree of a polyester resin composition means the ratio of the crystal part in matrix resin, and it can measure according to the method as described in the below-mentioned Example.
  • thermoplastic polyester resin (A) and the polyester resin composition in the present invention preferably have a mass average molecular weight and an absolute crystallinity within the ranges described above, and as the combination thereof, the thermoplastic polyester resin (A) When polybutylene terephthalate resin is used, the mass average molecular weight is preferably 70,000 to 150,000 and the absolute crystallinity is preferably 25% to 35%. The mass average molecular weight is 100,000 to 150,000 and the absolute crystallinity is 25 % Or more and 35% or less are more preferable.
  • thermoplastic polyester resin (A) is a polyethylene terephthalate resin
  • the mass average molecular weight is 30,000 to 150,000 and the absolute crystallinity is preferably 10% to 35%, and the mass average molecular weight is 40,000 to 150,000.
  • the absolute crystallinity is more preferably 20% or more and 35% or less.
  • thermoplastic polyester resin (A) is composed of a dicarboxylic acid component and a diol component, and can be obtained by a combination of polycondensation of the dicarboxylic acid component and the diol component.
  • the dicarboxylic acid component includes dicarboxylic acid and its lower ester derivative, and these are collectively referred to as a dicarboxylic acid component.
  • dicarboxylic acid component which constitutes thermoplastic polyester resin (A)
  • aliphatic dicarboxylic acid, alicyclic dicarboxylic acid, aromatic dicarboxylic acid, and dicarboxylic acid having a furan ring can be used.
  • examples thereof include terephthalic acid and the like, which are listed in paragraph 0014 of JP-A-2016-89148.
  • the dicarboxylic acid components can be used alone or in combination of two or more.
  • diol component which comprises a thermoplastic polyester resin (A)
  • an aliphatic diol an alicyclic diol, an aromatic diol, and the diol which has a furan ring
  • 1,4-butanediol and the like those listed in paragraph 0015 of JP-A-2016-89148 can be mentioned.
  • the diol components can be used alone or in combination of two or more.
  • an aromatic ring, an alicyclic ring, or a furan ring is a dicarboxylic acid or It is preferable to include it in one or both of the diols. Specific examples thereof include those listed in paragraph 0016 of JP-A-2016-89148.
  • the polycondensation of the dicarboxylic acid component and the diol component is not particularly limited, and can be carried out according to a known method.
  • the thermoplastic polyester resin (A) obtained has a glass transition temperature (Tg) of preferably 20 ° C. or more, more preferably 25 ° C. or more, still more preferably 30 ° C. or more, still more preferably, from the viewpoint of improving molding processability. 35 ° C or higher. Further, from the viewpoint of improving the vibration damping property, it is preferably 160 ° C. or less, more preferably 150 ° C. or less, still more preferably 140 ° C. or less, still more preferably 130 ° C. or less. In order for the glass transition temperature to be the above temperature, it is effective to control the skeleton structure of the polyester resin.
  • thermoplastic polyester resin when a thermoplastic polyester resin is prepared by using a rigid component such as an aromatic dicarboxylic acid component or an alicyclic diol component as a raw material, it is possible to increase the glass transition temperature.
  • the glass transition temperature of resin can be measured in accordance with the method as described in the below-mentioned Example.
  • the thermoplastic polyester resin (A) in this invention has crystallinity from a vibration suppression viewpoint.
  • a method of preparing a thermoplastic polyester resin having crystallinity a method using a dicarboxylic acid component and a diol component having high purity, and a method using a dicarboxylic acid component with a small amount of side chains and a diol component can be mentioned.
  • having crystallinity means heating the resin from 25 ° C. to 300 ° C. at a heating rate of 20 ° C./min according to JIS K 7122 (1999), and holding for 5 minutes in that state, Then, when cooled at ⁇ 20 ° C./min so as to be 25 ° C.
  • thermoplastic polyester resin (A) constituting the present invention preferably has a crystallization enthalpy ⁇ Hmc of 5 J / g or more, more preferably 10 J / g or more, still more preferably 15 J / g or more, still more preferably 30 J / g or more It is preferable to use a resin.
  • the crystallization enthalpy of resin can be measured according to the method as described in the below-mentioned Example.
  • thermoplastic polyester resin (A) examples include, for example, those listed in paragraph 0020 of JP-A-2016-89148, and from the viewpoint of damping property, terephthalic acid and 1,4-butanediol Preferred is polybutylene terephthalate (PBT resin, Tg: 50 ° C.).
  • PBT resin polybutylene terephthalate
  • the thermoplastic polyester resins (A) can be used alone or in combination of two or more.
  • the content of the thermoplastic polyester resin (A) is preferably 50% by mass or more, more preferably 55% by mass or more, and still more preferably 60% by mass or more from the viewpoint of improving the loss coefficient. Further, from the viewpoint of improving the rigidity, 90% by mass or less is preferable, 80% by mass or less is more preferable, 75% by mass or less is more preferable, and 70% by mass or less is more preferable.
  • the mass average molecular weight of the thermoplastic polyester resin (A) is preferably 30,000 or more, more preferably 50,000 or more, still more preferably 70,000 or more, from the viewpoint of improving the damping property. From the viewpoint of improving the properties, it is preferably at most 300,000, more preferably at most 200,000, further preferably at most 150,000. Specifically, the mass average molecular weight of the thermoplastic polyester resin (A) is measured by the method described in the following examples.
  • Component (B) which is a plasticizer and / or an elastomer As a component (B) in this invention, 1 type (s) or 2 or more types selected from the group which consists of a plasticizer and an elastomer are used. In the present specification, the plasticizer and / or the elastomer may be collectively referred to as component (B).
  • the plasticizer in the present invention contains one or more selected from the group consisting of polyester plasticizers, polyhydric alcohol ester plasticizers, polyhydric carboxylic acid ester plasticizers, and bisphenol plasticizers. Is preferred.
  • plasticizers having a 5% mass loss temperature of 200 ° C. or more are preferable, plasticizers of 220 ° C. or more are more preferable, plasticizers of 240 ° C. or more are more preferable, and plasticizers of 260 ° C. or more are more preferable.
  • the measurement of the 5% mass loss temperature of the plasticizer is carried out under the condition that the temperature is raised at 10 ° C./min in an air atmosphere.
  • the weight retention of the plasticizer at 260 ° C. in an air atmosphere for 5 minutes isothermally maintained is preferably 80% or more, more preferably 85% or more, and still more preferably 90% or more. From the viewpoint of improving, it is preferably 100% or less, more preferably 98% or less.
  • polyester plasticizer examples include those listed in paragraph 0024 of JP-A-2016-89148.
  • Preferred examples include, for example, mixed diesters of adipic acid and diethylene glycol monomethyl ether / benzyl alcohol.
  • polyhydric alcohol ester plasticizer examples include those listed in paragraph 0025 of JP-A-2016-89148.
  • polyvalent carboxylic acid ester plasticizers examples include those listed in paragraph 0026 of JP-A-2016-89148.
  • Examples of the bisphenol-based plasticizer include those listed in paragraph 0027 of JP-A-2016-89148.
  • a polyester-based plasticizer from the viewpoint of improving the loss coefficient, a polyester-based plasticizer, a polyhydric alcohol ester-based plasticizer, a polyvalent carboxylic acid, preferably having a (poly) oxyalkylene group or an alkylene group having 2 to 10 carbon atoms
  • the (poly) oxyalkylene group means an oxyalkylene group or a polyoxyalkylene group.
  • the oxyalkylene group is preferably one having an alkylene group having preferably 2 to 10 carbon atoms, more preferably 2 to 6 carbon atoms, and still more preferably 2 to 4 carbon atoms, and an oxyethylene group, an oxypropylene group or an oxybutylene group Preferably, oxyethylene or oxypropylene is more preferred.
  • the plasticizer preferably contains one or more selected from the group consisting of the following compound groups (A) to (C) from the viewpoint of improving the loss coefficient, and the following compound group (A) It is more preferable to contain one or more selected from the group consisting of and (B).
  • Compound Group (A) An ester compound having two or more ester groups in the molecule, wherein at least one of the alcohol components constituting the ester compound has an average of 0 to 2 alkylene oxides per one hydroxyl group.
  • ester compound group (B) Formula (I): R 1 O-CO-R 2 -CO-[(OR 3 ) m O-CO-R 2 -CO-] n OR 1 (I) (Wherein, R 1 is an alkyl group having 1 to 4 carbon atoms, R 2 is an alkylene group having 2 to 4 carbon atoms, R 3 is an alkylene group having 2 to 6 carbon atoms, and m is 1 to 6) And n represents a number of 1 to 12, provided that all R 2 s may be the same or different, and all R 3 s may be the same or different)
  • Compound compound group (C) represented by: an ester compound having two or more ester groups in the molecule, wherein the alcohol component constituting the ester compound is a monoalcohol
  • the ester compound contained in the compound group (A) is a polyhydric alcohol ester or polyhydric carboxylic acid ether ester having two or more ester groups in the molecule, and at least one of alcohol components constituting the ester compound.
  • An ester compound which is an alcohol having an average of 0.5 to 5 moles of an alkylene oxide of 2 to 3 carbon atoms added per hydroxyl group is preferable.
  • R 1 in the formula (I) represents an alkyl group having 1 to 4 carbon atoms, and two in one molecule are present at both ends of the molecule.
  • R 1 may be linear or branched as long as it has 1 to 4 carbon atoms.
  • the carbon number of the alkyl group is preferably 1 to 4 and more preferably 1 to 2 from the viewpoint of exhibiting coloring resistance and a plasticizing effect.
  • methyl group, ethyl group, propyl group, isopropyl group, butyl group, sec-butyl group, tert-butyl group, iso-butyl group can be mentioned, and among them, from the viewpoint of improving the loss factor, methyl A group and an ethyl group are preferable, and a methyl group is more preferable.
  • R 2 in the formula (I) represents an alkylene group having 2 to 4 carbon atoms, and a linear alkylene group is mentioned as a preferable example. Specifically, ethylene, 1,3-propylene and 1,4-butylene are mentioned, and from the viewpoint of improving the loss factor, ethylene, 1,3-propylene and 1,4-butylene are preferable. Preferably, ethylene is more preferred. However, all R 2 s may be the same or different.
  • R 3 in the formula (I) represents an alkylene group having 2 to 6 carbon atoms, and OR 3 is present as an oxyalkylene group in the repeating unit.
  • R 3 may be linear or branched as long as it has 2 to 6 carbon atoms.
  • the number of carbon atoms of the alkylene group is preferably 2 to 6, and more preferably 2 to 3 from the viewpoint of improving the loss coefficient.
  • M represents the average number of repetition of the oxyalkylene group, and from the viewpoint of heat resistance, the number is preferably 1 to 6, more preferably 1 to 4, and still more preferably 1 to 3.
  • N represents the average number of repeating units (average degree of polymerization) of the repeating units, and is a number of 1 to 12.
  • the damping material is preferably a number of 1 to 12, more preferably a number of 1 to 6, and still more preferably a number of 1 to 5 from the viewpoint of improving the loss coefficient.
  • the average degree of polymerization may be determined by analysis such as NMR, but can be calculated according to the method described in paragraph 0100 of JP-A 2016-89148.
  • R 1 is all methyl group
  • R 2 is ethylene group or 1,4-butylene group
  • R 3 is ethylene group or 1,3-propylene group
  • m is a number of 1 to 4 and n is a number of 1 to 6
  • R 1 is all methyl
  • R 2 is ethylene or 1,4-butylene
  • R 3 is ethylene or 1
  • Compounds having a 3-propylene group, m being a number of 1 to 3 and n being a number of 1 to 5 are more preferable.
  • the compound represented by the formula (I) is not particularly limited as long as it has the above-mentioned structure, but a compound obtained by reacting the following (1) to (3) is preferable.
  • (1) and (2), or (2) and (3) may form an ester compound.
  • (2) may be an acid anhydride or an acid halide.
  • a monohydric alcohol having alkyl group having 1 to 4 carbon atoms is an alcohol containing the above R 1 , specifically, methanol, Ethanol, 1-propanol, 2-propanol, 1-butanol, 2-butanol, 2-methyl-1-propanol, tert-butanol can be mentioned.
  • methanol, ethanol, 1-propanol and 1-butanol are preferable, methanol and ethanol are more preferable, and methanol is still more preferable from the viewpoint of improving the loss factor.
  • the dicarboxylic acid having an alkylene group having 2 to 4 carbons is a dicarboxylic acid containing the above-mentioned R 2.
  • succinic acid, Glutaric acid, adipic acid and their derivatives such as succinic anhydride, glutaric anhydride, dimethyl succinate, dibutyl succinate, dimethyl glutarate, dimethyl adipate and the like can be mentioned.
  • succinic acid, adipic acid and derivatives thereof for example, succinic anhydride, dimethyl succinate, dibutyl succinate, dimethyl adipate are preferable, and succinic acid and its derivatives, for example, Succinic anhydride, dimethyl succinate and dibutyl succinate are more preferred.
  • Dihydric alcohol having an alkylene group having 2 to 6 carbon atoms is a dihydric alcohol containing the above R 3 , specifically, Ethylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol, 1,2-propanediol, 1,3-propanediol, 2-methyl-1,3-propanediol, 2,2-dimethyl-1,3-propanediol 1,2-butanediol, 1,3-butanediol, 1,4-butanediol, 1,2-pentanediol, 1,4-pentanediol, 1,5-pentanediol, 2,5-hexanediol, Examples include 1,6-hexanediol and 3-methyl-1,5-pentanediol.
  • diethylene glycol, triethylene glycol, 1,2-propanediol, 1,3-propanediol, tetraethylene glycol and 1,4-butanediol are preferable from the viewpoint of improving the loss coefficient, and diethylene glycol and triethylene glycol, 1,2-propanediol and 1,3-propanediol are more preferable, and diethylene glycol, triethylene glycol and 1,3-propanediol are more preferable.
  • the monohydric alcohol is one or more selected from the group consisting of methanol, ethanol, 1-propanol, and 1-butanol
  • the dicarboxylic acid is succinic acid, adipic acid, glutaric acid, and And one or more selected from the group consisting of derivatives thereof
  • the dihydric alcohol is diethylene glycol, triethylene glycol, 1,2-propanediol, 1,3-propanediol, tetraethylene glycol, and Preferably, it is one or more selected from the group consisting of 1,4-butanediol, (1) One or two or more selected from the group consisting of methanol and ethanol, and (2) One or more selected from the group consisting of succinic acid, adipic acid, and derivatives thereof More than two, and (3) the dihydric alcohol is one or more selected from the group consisting of diethylene glycol, triethylene glycol, 1,2-propanediol, and 1,
  • Embodiment 1 A step of esterification reaction of (2) dicarboxylic acid and (1) monohydric alcohol to synthesize a dicarboxylic acid ester, and a step of esterifying reaction of the obtained dicarboxylic acid ester and (3) dihydric alcohol
  • Method aspect 2 including: Method including batch reaction of (1) monohydric alcohol, (2) dicarboxylic acid, and (3) dihydric alcohol
  • the method of aspect 1 is preferable from the viewpoint of adjusting the average degree of polymerization.
  • reaction of each process mentioned above can be performed according to a well-known method.
  • the compound represented by the formula (I) is preferably 1.50 mg KOH / g or less, more preferably 1.00 mg KOH / g or less, from the viewpoint of improving the loss coefficient, and the hydroxyl value is a loss coefficient From the viewpoint of improving the pH, it is preferably 10.0 mg KOH / g or less, more preferably 5.0 mg KOH / g or less, and still more preferably 3.0 mg KOH / g or less.
  • the acid value and the hydroxyl value of the plasticizer can be measured according to the method described in paragraph 0099 of JP-A-2016-89148.
  • the number average molecular weight of the compound represented by the formula (I) is preferably 300 to 1,500, more preferably 300 to 1000, from the viewpoint of color resistance, from the viewpoint of improving the loss coefficient.
  • the number average molecular weight of the plasticizer can be calculated according to the method described in paragraph 0100 of JP-A-2016-89148.
  • the saponification value of the compound represented by the formula (I) is preferably 500 to 800 mg KOH / g, and more preferably 550 to 750 mg KOH / g from the viewpoint of improving the loss coefficient.
  • the saponification value of the plasticizer can be measured according to the method described in paragraph 0099 of JP-A-2016-89148.
  • the compound represented by the formula (I) preferably has an alkyl esterification ratio (terminal alkyl esterification ratio) to two molecular ends of 95% or more, more preferably 98% or more. It is.
  • the terminal alkyl esterification rate of the plasticizer can be calculated according to the method described in paragraph 0100 of JP-A 2016-89148.
  • the ether group value of the compound represented by the formula (I) is preferably 0 to 8 mmol / g, and more preferably 0 to 6 mmol / g.
  • the ether group value of the plasticizer can be calculated according to the method described in paragraph 0100 of JP-A-2016-89148.
  • the ester compound contained in the compound group (C) is preferably an ester of adipic acid and 2-ethylhexanol (DOA) and an ester of phthalic acid and 2-ethylhexanol (DOP).
  • DOA 2-ethylhexanol
  • DOP 2-ethylhexanol
  • the content of one or more selected from the group consisting of polyester plasticizers, polyhydric alcohol ester plasticizers, polyhydric carboxylic acid ester plasticizers, and bisphenol plasticizers preferably It is selected from the group consisting of polyester-based plasticizers, polyhydric alcohol ester-based plasticizers, polyvalent carboxylic acid ester-based plasticizers, and bisphenol-based plasticizers having a poly (oxyalkylene) group or an alkylene group having 2 to 10 carbon atoms.
  • polyester plasticizers polyhydric alcohol ester plasticizers, polyhydric carboxylic acid ester plasticizers, and bisphenol plasticizers having one or more contents, more preferably (poly) oxyalkylene groups A group consisting of one or more selected from the group consisting of: and such compound groups (A) to (C)
  • the content of one or more compounds selected is preferably 50% by mass or more, more preferably 80% by mass or more, still more preferably 90% by mass or more, further preferably from the viewpoint of improving the loss coefficient. It is 95% by mass or more, more preferably substantially 100% by mass, and still more preferably 100% by mass.
  • substantially 100% by mass means a state in which a trace amount of impurities and the like are inevitably contained.
  • the content of the plasticizer means the total content when a plurality of compounds are contained.
  • the content of the plasticizer is preferably 1 part by mass or more, more preferably 3 parts by mass or more, still more preferably 5 parts by mass from the viewpoint of improving the loss coefficient with respect to 100 parts by mass of the thermoplastic polyester resin (A).
  • the amount is more preferably 10 parts by mass or more, and preferably 50 parts by mass or less, more preferably 40 parts by mass or less, still more preferably 30 parts by mass or less, still more preferably 25 parts by mass or less from the viewpoint of suppressing rigidity reduction. is there.
  • the content of the plasticizer in the polyester resin composition is preferably 1% by mass or more, more preferably 3% by mass or more, still more preferably 5% by mass or more, from the viewpoint of improving the loss coefficient From the viewpoint of suppression, it is preferably 25% by mass or less, more preferably 20% by mass or less, and still more preferably 15% by mass or less.
  • thermoplastic elastomer In the present invention, one or two or more elastomers are used from the viewpoint of the improvement of the damping property in the high temperature range and the low temperature range.
  • a thermoplastic elastomer As an elastomer in the present invention, a thermoplastic elastomer is preferable.
  • the content of the elastomer is preferably 10 parts by mass or more, more preferably 12 parts by mass or more, and 15 parts by mass with respect to 100 parts by mass of the thermoplastic polyester resin (A), from the viewpoint of improving the loss coefficient in the low temperature range.
  • the above is more preferable.
  • 50 mass parts or less are preferable, 40 mass parts or less are more preferable, and 35 mass parts or less are still more preferable.
  • the content of the elastomer in the polyester resin composition is preferably 5% by mass or more, more preferably 8% by mass or more, and still more preferably 9.5% by mass or more, from the viewpoint of improving the loss coefficient
  • a plasticizer and an elastomer may be used in combination, and it is possible to use a plasticizer alone or two or more types and an elastomer alone or a combination of two or more types.
  • a plasticizer and an elastomer in combination, the loss coefficient in the room temperature region is further improved, and the loss coefficient is also improved in a wide temperature region such as a low temperature region or a high temperature region.
  • the total content of the plasticizer and the elastomer in combination is preferably 15 parts by mass or more, and more preferably 20 parts by mass or more with respect to 100 parts by mass of the thermoplastic polyester resin (A). 25 parts by mass or more is more preferable. Moreover, from a viewpoint of rigidity fall suppression, 60 mass parts or less are preferable, 50 mass parts or less are more preferable, and 40 mass parts or less are still more preferable.
  • the mass ratio of plasticizer and elastomer (plasticizer / elastomer) at the time of combined use is preferably 30/70 to 70/30, and 40/60 to 60/40 from the viewpoint of improving the loss coefficient in a wide temperature range. More preferable.
  • thermoplastic elastomer Use of a thermoplastic elastomer as the elastomer is preferable because the effect of improving the damping properties in the high temperature range and the low temperature range is exhibited. Furthermore, by using together with the plasticizer, the vibration damping property can be further improved in a wide temperature range in the high temperature range and the low temperature range.
  • the thermoplastic elastomer preferably has a glass transition temperature Tg of ⁇ 40 ° C. or higher, and preferably 20 ° C. or lower, from the viewpoint of improving the damping performance in the high temperature range and the low temperature range.
  • Tg glass transition temperature
  • the glass transition temperature of the thermoplastic elastomer can be measured according to the method described in the examples below.
  • the thermoplastic elastomer in the present invention includes styrene thermoplastic elastomer, olefin thermoplastic elastomer, polyester thermoplastic elastomer, polyamide thermoplastic elastomer, urethane thermoplastic elastomer, nitrile thermoplastic elastomer, fluorine thermoplastic elastomer And at least one selected from polybutadiene-based thermoplastic elastomers and silicone-based thermoplastic elastomers, and as styrene-based thermoplastic elastomers, polystyrene-vinyl-polyisoprene-polystyrene block copolymer, copolymer of styrene and butadiene, and
  • the hydrogen additive can be mentioned, for example, “Hybler” manufactured by Kuraray Plastics, “Tough Tech” “S.O.E” (registered trademark) manufactured by Asahi Kasei Co., Ltd., Formula company
  • olefin-based thermoplastic elastomer examples include those in which an olefin-based rubber (EPR, EPDM) is finely dispersed in a matrix of an olefin-based resin (polyethylene, polypropylene, etc.). Trademarks, "Espolex” (registered trademark) manufactured by Sumitomo Chemical Co., Ltd., and the like.
  • polyester-based thermoplastic elastomers include copolymers of polybutylene terephthalate and polyether and the like, and examples thereof include Hytrel (registered trademark) manufactured by Toray DuPont Co., Ltd.
  • polyamide-based thermoplastic elastomers include those obtained by transesterification and condensation polymerization reactions using block copolymers of nylon and polyester or polyol, lactams, and dicarboxylic acid polyether diols as raw materials.
  • urethane type thermoplastic elastomer there is, for example, "TPU” manufactured by Nippon Polyurethane Industry Co., Ltd.
  • thermoplastic elastomer As a nitrile thermoplastic elastomer, what emulsion-polymerized acrylonitrile and butadiene, etc. are mentioned.
  • fluorine-based thermoplastic elastomer include copolymers of vinylidene fluoride and hexafluoropropylene, copolymers of vinylidene fluoride, hexafluoropropylene and tetrafluoroethylene, etc.
  • fluorine-based thermoplastic elastomer include copolymers of vinylidene fluoride and hexafluoropropylene, copolymers of vinylidene fluoride, hexafluoropropylene and tetrafluoroethylene, etc.
  • Showa Highpolymer Co., Ltd. There are "Eraftol” (registered trademark), DuPont “Viton” (registered trademark) series, and the like
  • Polybutadiene-based and silicone-based thermoplastic elastomers include organic silicon polymer bonds in which an organic group or the like is directly bonded to the silicon atom with a siloxane bond as a skeleton, and examples thereof include KBM series made by Shin-Etsu Silicone.
  • a thermoplastic elastomer a styrene-based thermoplastic elastomer is preferable from the viewpoint of the improvement of the damping property in the high temperature range and the low temperature range.
  • styrenic thermoplastic elastomer (Styrenic thermoplastic elastomer) in the present invention, block A formed by polymerization of a styrenic compound constituting the hard segment, and conjugated diene constituting the soft segment are polymerized.
  • the block B is composed of Examples of the styrene compound used for the polymer block A include styrene compounds such as styrene, ⁇ -methylstyrene, o-methylstyrene, m-methylstyrene, p-methylstyrene and 1,3-dimethylstyrene; vinyl naphthalene, Polycyclic aromatic compounds having a vinyl group such as vinyl anthracene and the like are mentioned, and among these, polymers of styrene compounds are preferable, and polymers of styrene are more preferable.
  • styrene compounds such as styrene, ⁇ -methylstyrene, o-methylstyrene, m-methylstyrene, p-methylstyrene and 1,3-dimethylstyrene
  • vinyl naphthalene Polycyclic aromatic compounds having a vinyl group such as vinyl anthracene and
  • the conjugated diene used for the polymer block B includes, for example, butadiene, isoprene, butylene, ethylene, 1,3-pentadiene, 2,3-dimethyl-1,3-butadiene and the like, preferably polyisoprene, polybutadiene, and The copolymer of isoprene and butadiene is mentioned, It is the block copolymer which superposed
  • a styrenic compound used for the polymer block A may be copolymerized. In the case of each copolymer, any form of a random copolymer, a block copolymer, and a tapered copolymer can be selected as the form thereof. Alternatively, a hydrogenated structure may be used.
  • styrenic elastomers include polystyrene-isoprene block copolymer (SIS), polystyrene-polybutadiene copolymer (SEBS), polystyrene-hydrogenated polybutadiene copolymer (SEBS), polystyrene-hydrogenated Polyisoprene-polystyrene block copolymer (SEPS), polystyrene-vinyl-polyisoprene-polystyrene block copolymer (SHIVS), polystyrene-hydrogenated polybutadiene-hydrogenated polyisoprene-polystyrene block copolymer, polystyrene-hydrogenated polybutadiene -Polyisoprene-polystyrene block copolymer etc.
  • SIS polystyrene-isoprene block copolymer
  • SEBS polystyrene
  • polystyrene-vinyl-polyisoprene-polystyrene block copolymer is preferably used in the present invention, and commercially available products of such block copolymers include “Hylar” series manufactured by Kuraray Plastics Co., Ltd. .
  • the styrene content in the styrenic elastomer is preferably 10% by mass or more, more preferably 15% by mass or more, preferably 30% by mass or less, from the viewpoint of improving the damping performance in the high temperature range and the low temperature range. Preferably it is 25 mass% or less.
  • the high temperature range means 35 to 80 ° C.
  • the low temperature range means -20 to 10 ° C.
  • the styrene content in the styrenic elastomer is described in the following examples. It can be measured according to the method of
  • styrene-type elastomer a styrene isoprene block copolymer and / or a styrene butadiene block copolymer are preferable.
  • the styrene isoprene block copolymer in the present invention is a block copolymer having a polystyrene block at both ends, and having at least one block of a polyisoprene block or a vinyl-polyisoprene block therebetween.
  • an isoprene block or a butadiene block may be copolymerized or may have a hydrogenated structure.
  • styrene-isoprene block copolymer examples include polystyrene-isoprene block copolymer (SIS), polystyrene-hydrogenated polyisoprene-polystyrene block copolymer (SEPS), polystyrene-vinyl-polyisoprene Polystyrene block copolymer (SHIVS), polystyrene-hydrogenated polybutadiene-hydrogenated polyisoprene-polystyrene block copolymer, polystyrene-hydrogenated polybutadiene-polyisoprene-polystyrene block copolymer, and the like.
  • SIS polystyrene-isoprene block copolymer
  • SEPS polystyrene-hydrogenated polyisoprene-polystyrene block copolymer
  • SHIVS polystyrene-viny
  • polystyrene-vinyl-polyisoprene-polystyrene block copolymer is preferably used in the present invention, and commercially available products of such block copolymers include “Hylar” series manufactured by Kuraray Plastics Co., Ltd. .
  • the styrene butadiene block copolymer in the present invention is a block copolymer having a polystyrene block at both ends and having a polybutadiene block or a hydrogenated substance thereof in between.
  • an isoprene block or a butadiene block may be copolymerized or may have a hydrogenated structure.
  • styrene-butadiene block copolymer examples include polystyrene-polybutadiene copolymer (SEBS), polystyrene-hydrogenated polybutadiene copolymer (SEBS), polystyrene-polybutadiene copolymer (SBS), polystyrene And hydrogenated polybutadiene copolymers (SBS) and the like. These may be used alone or in combination of two or more.
  • SEBS polystyrene-polybutadiene copolymer
  • SEBS polystyrene-hydrogenated polybutadiene copolymer
  • SBS polystyrene-polybutadiene copolymer
  • SBS polystyrene And hydrogenated polybutadiene copolymers
  • SEBS polystyrene-hydrogenated polybutadiene copolymer
  • elastomers with few or no unsaturated bonds are preferable.
  • the thing hydrogenated among various said elastomers is mentioned.
  • an elastomer that is resistant to oxidative degradation or does not undergo oxidative degradation is preferable.
  • the thing hydrogenated among various said elastomers is mentioned.
  • the polyester resin composition in the present invention contains an inorganic filler (C) from the viewpoint of rigidity improvement.
  • the inorganic filler (C) in the present invention is not particularly limited as long as it is a known inorganic filler, and is an inorganic filler generally used for reinforcing a thermoplastic resin, specifically, a plate-like filler, One or more selected from the group consisting of granular fillers, acicular fillers, and fibrous fillers can be used.
  • the plate-like filler has an aspect ratio (length of the longest side of the largest surface of the plate-like body / thickness of the surface) of 20 or more and 150 or less.
  • the length of the plate-like filler (length of the longest side in the largest surface) It is preferably 1.0 ⁇ m or more, more preferably 5 ⁇ m or more, still more preferably 10 ⁇ m or more, further preferably 20 ⁇ m or more, preferably 150 ⁇ m or less, more preferably 100 ⁇ m or less, further preferably 50 ⁇ m or less, still more preferably 40 ⁇ m or less More preferably, it is 30 ⁇ m or less.
  • the thickness is not particularly limited, but from the same viewpoint, preferably 0.01 ⁇ m or more, more preferably 0.05 ⁇ m or more, still more preferably 0.1 ⁇ m or more, still more preferably 0.2 ⁇ m or more, preferably 5 ⁇ m or less. More preferably, it is 3 ⁇ m or less, still more preferably 2 ⁇ m or less, still more preferably 1 ⁇ m or less, and still more preferably 0.5 ⁇ m or less.
  • the aspect ratio of the plate-like filler is preferably 30 or more, more preferably 40 or more, still more preferably 50 or more, and preferably 120 or less, more preferably 100 or less, from the same viewpoint. Preferably it is 90 or less, More preferably, it is 80 or less.
  • the plate-like filler examples include, for example, those listed in paragraph 0064 of JP-A-2016-89148, such as mica.
  • the side length and thickness of a plate-shaped filler can be calculated
  • the particulate filler is not limited to those having a spherical shape, but also to those having a cross-sectional elliptical or substantially oval shape, and has an aspect ratio (longest diameter of granular body / shortest diameter of granular body) One or more and less than two, and one close to one is preferable.
  • the average particle diameter of the particulate filler is preferably 1.0 ⁇ m or more, more preferably from the viewpoint of obtaining good dispersibility in the polyester resin composition, improving the flexural modulus, and / or improving the loss factor.
  • the thickness is 5 ⁇ m or more, more preferably 10 ⁇ m or more, further preferably 20 ⁇ m or more, preferably 50 ⁇ m or less, more preferably 40 ⁇ m or less, and still more preferably 30 ⁇ m or less.
  • Specific examples of the particulate filler include those listed in paragraph 0065 of JP-A-2016-89148.
  • the diameter of the particulate filler can be determined by cutting 100 fillers randomly selected, observing the cross section with an optical microscope, and calculating the number average.
  • the needle-like filler has an aspect ratio (particle length / particle diameter) in the range of 2 or more and less than 20.
  • the length (particle length) of the needle-like filler is preferably 1.0 ⁇ m from the viewpoint of obtaining good dispersibility in the polyester resin composition, improving the flexural modulus, and / or improving the loss factor. Or more, more preferably 5 ⁇ m or more, still more preferably 10 ⁇ m or more, still more preferably 20 ⁇ m or more, still more preferably 30 ⁇ m or more, preferably 150 ⁇ m or less, more preferably 100 ⁇ m or less, still more preferably 80 ⁇ m or less, more preferably 60 ⁇ m or less It is.
  • the particle diameter is not particularly limited, but from the same viewpoint, preferably 0.01 ⁇ m or more, more preferably 0.1 ⁇ m or more, still more preferably 0.5 ⁇ m or more, preferably 20 ⁇ m or less, more preferably 15 ⁇ m or less, further Preferably it is 10 micrometers or less.
  • the aspect ratio of the needle-like filler is preferably 5 or more, and preferably 10 or less from the same viewpoint. Specific examples of the needle-like filler include those listed in paragraph 0066 of JP-A-2016-89148.
  • the particle length and particle diameter of the needle-like filler can be determined by observing 100 fillers randomly selected with an optical microscope and calculating the number average. When the particle size has a minor axis and a major axis, the major axis is used to calculate.
  • the fibrous filler is one having an aspect ratio (average fiber length / average fiber diameter) of more than 150.
  • the length (average fiber length) of the fibrous filler is preferably 0.15 mm or more, more preferably 0.2 mm or more, and still more preferably 0.5 mm or more, from the viewpoint of improving bending modulus and loss coefficient. More preferably, it is 1 mm or more, preferably 30 mm or less, more preferably 10 mm or less, and still more preferably 5 mm or less.
  • the average fiber diameter is not particularly limited, but from the same viewpoint, it is preferably 1 ⁇ m or more, more preferably 3 ⁇ m or more, preferably 30 ⁇ m or less, more preferably 20 ⁇ m or less, further preferably 10 ⁇ m or less.
  • the aspect ratio is preferably 200 or more, more preferably 250 or more, still more preferably 500 or more, and preferably 10000 or less, more preferably 5000 or less, still more preferably 1000 or less, from the same viewpoint. More preferably, it is 800 or less.
  • Specific examples of fibrous fillers include those listed in paragraph 0067 of JP-A-2016-89148.
  • the fiber length and fiber diameter of a fibrous filler can be calculated
  • the fibrous filler is cut by the shear force in the kneading section and the average is Although the fiber length is shortened, the average fiber length of the fibrous filler in the resin is preferably 100 to 800 ⁇ m, more preferably 200 to 700 ⁇ m, and still more preferably 300 to 600 ⁇ m from the viewpoint of improving the loss coefficient and rigidity.
  • the granular, plate-like or needle-like filler may be coated or converged with a thermoplastic resin such as ethylene / vinyl acetate copolymer or a thermosetting resin such as epoxy resin, aminosilane or epoxy It may be treated with a coupling agent such as silane.
  • a thermoplastic resin such as ethylene / vinyl acetate copolymer or a thermosetting resin such as epoxy resin, aminosilane or epoxy It may be treated with a coupling agent such as silane.
  • fillers can be used alone or in combination of two or more, and fillers of different shapes may be combined.
  • at least one selected from the group consisting of a plate-like filler, a needle-like filler, and a fibrous filler from the viewpoint of improving the flexural modulus and suppressing the decrease in loss coefficient. More preferably, it is 1 type, or 2 or more types selected from the group which consists of a plate-like filler and a needle-like filler, More preferably, it is 1 type or 2 or more types of a plate-like filler.
  • mica, talc and glass fiber are preferably used, mica and talc are more preferably used, and mica is more preferably used.
  • the plate-like filler is oriented in the direction of flow in the injection-molded product, etc., so the tensile modulus in the direction of orientation and the flexural modulus in the direction perpendicular to the direction of orientation are significantly improved compared to other fillers. Also, it is presumed that the loss coefficient is further suppressed because there are many interfaces that affect the friction generated when the molded body vibrates.
  • the content of the plate-like filler in the inorganic filler is preferably 60% by mass or more, more preferably 80% by mass or more, and still more preferably 90% by mass or more from the viewpoint of suppressing the loss coefficient decrease.
  • the content of the inorganic filler (C) is preferably 10 parts by mass or more, more preferably 15 parts by mass or more, and 20 parts by mass or more with respect to 100 parts by mass of the thermoplastic polyester resin (A). Is more preferable, and 30 parts by mass or more is further preferable. Further, from the viewpoint of suppressing a decrease in loss factor, 80 parts by mass or less is preferable, 70 parts by mass or less is more preferable, 60 parts by mass or less is more preferable, 50 parts by mass or less is more preferable, 45 parts by mass or less is more preferable .
  • content of an inorganic filler is the total mass of the inorganic filler used, and when several compounds are contained, it means the thing of total content.
  • the content of the inorganic filler is preferably 5% by mass or more, more preferably 10% by mass or more, still more preferably 15% by mass or more, further preferably 20% by mass from the viewpoint of rigidity improvement.
  • the mass ratio of the component (B) to the inorganic filler (C) is 10/90 to 60 / from the viewpoint of improving the elastic modulus and the loss factor.
  • 40 is preferable, 25/75 to 50/50 is more preferable, and 40/60 to 47/53 is further preferable.
  • the polyester resin composition in the present invention can contain an organic crystal nucleating agent from the viewpoint of improving the crystallization rate of the polyester resin, improving the crystallinity of the polyester resin, and improving the flexural modulus.
  • organic crystal nucleating agent known organic crystal nucleating agents can be used, and organic carboxylic acid metal salts, organic sulfonic acid salts, carboxylic acid amides, phosphorus compound metal salts, metal salts of rosins, alkoxy metal salts, And organic nitrogen-containing compounds can be used. Specifically, for example, those listed in paragraph 0074 of JP-A-2016-89148 can be mentioned.
  • the content of the organic crystal nucleating agent (D) is preferably 0.01 parts by mass or more, more preferably 100 parts by mass of the thermoplastic polyester resin (A), from the viewpoint of improving the bending elastic modulus and the loss coefficient. Is 0.1 parts by mass or more, more preferably 0.2 parts by mass or more, preferably 20 parts by mass or less, more preferably 10 parts by mass or less, from the viewpoint of improving flexural modulus and loss factor Is 5 parts by mass or less, more preferably 3 parts by mass or less, still more preferably 1 part by mass or less.
  • the content of the organic crystal nucleating agent means the total content of all the organic crystal nucleating agents contained in the polyester resin composition.
  • the polyester resin composition in the present invention is a lubricant other than the above components, which is a lubricant, an inorganic crystal nucleating agent, a hydrolysis inhibitor, a flame retardant, an antioxidant, a hydrocarbon wax and an anionic surfactant.
  • An ultraviolet absorber, an antistatic agent, an antifogging agent, a light stabilizer, a pigment, an antifungal agent, an antibacterial agent, a foaming agent, etc. can be contained in the range which does not impair the effect of the present invention.
  • the polyester resin composition in the present invention may be prepared without particular limitation as long as it contains a thermoplastic polyester resin (A), a component (B) which is a plasticizer and / or an elastomer, and an inorganic filler (C).
  • a thermoplastic polyester resin A
  • a component (B) which is a plasticizer and / or an elastomer B
  • an inorganic filler C
  • materials such as thermoplastic polyester resin, plasticizer and / or elastomer, and inorganic filler, and, if necessary, various additives, may be sealed kneader, single- or twin-screw extruder, open-roll type kneader, etc.
  • the composition can be prepared by melt-kneading using a known kneader.
  • the melt-kneaded product may be dried or cooled according to a known method.
  • the raw materials can also be subjected to melt-kneading after being uniformly mixed in advance using a Henschel mixer, a super mixer, or the like.
  • a supercritical gas may be made to melt-mix.
  • the melt-kneading temperature is not generally set depending on the type of thermoplastic polyester resin to be used, but from the viewpoint of improving the moldability and prevention of deterioration of the polyester resin composition, it is preferably 220 ° C. or more, more preferably 225 ° C. or more It is preferably 230 ° C. or more, preferably 300 ° C. or less, more preferably 290 ° C. or less, still more preferably 280 ° C. or less, still more preferably 260 ° C. or less, still more preferably 250 ° C. or less, more preferably 240 ° C. or less .
  • the melt-kneading time can not be determined generally depending on the melt-kneading temperature and the type of the kneader, but it is preferably 15 to 900 seconds.
  • the laminated sheet of the present invention can be produced by a conventionally known method. For example, a method in which each layer is separately formed in advance and then laminated or thermocompression-pressed, a method in which the upper or lower surface of the previously formed layer is coated to form another layer, and respective resin layers are laminated by coextrusion And the like.
  • a method will be described more specifically, in which each layer is separately formed in advance, each layer is stacked, and then thermocompression bonding is performed.
  • a sheet-like molded article molded from a polycarbonate resin composition used as a polycarbonate layer is to obtain a desired thickness by a known method such as inflation molding, extrusion sheet molding, press molding, cast molding and the like. Can.
  • ⁇ Production of the first damping layer> Producing a first damping layer of a desired thickness by, for example, feeding the melt-kneaded product of the polyester resin composition prepared as described above to a known extruder or drawing machine and drawing it. Can.
  • the second damping layer can also be manufactured in the same manner as the first damping layer.
  • thermocompression bonding press The layers produced as described above are superimposed in a predetermined order. Set in a press, press-fit under the conditions of pressure 1 to 7MPa, temperature 170 to 190 ° C, press time 0.5 to 2.0 minutes, and then water cool to normal temperature to obtain a predetermined laminated sheet Can.
  • pressure 1 to 7MPa pressure 1 to 7MPa
  • temperature 170 to 190 ° C press time 0.5 to 2.0 minutes
  • water cool to normal temperature to obtain a predetermined laminated sheet Can.
  • changes in the thickness of the polycarbonate layer and the damping layer are almost negligible before and after the pressing.
  • the present invention further discloses the following laminated sheet.
  • ⁇ 2> A laminated sheet including the laminated structure according to ⁇ 1>.
  • the total thickness of the ⁇ 3> damping layer is 100%
  • the total thickness of the polycarbonate layer is 100% or more, preferably 200% or more, more preferably 300% or more, and 2000% or less, preferably 1000
  • ⁇ 4> The laminate according to any one of ⁇ 1> to ⁇ 3>, wherein a polycarbonate layer is further laminated on the upper surface of the first damping layer or the lower surface of the second damping layer. Sheet.
  • the thickness of the entire ⁇ 7> laminated sheet is preferably 0.3 mm or more, more preferably 1.0 mm or more, still more preferably 1.5 mm or more, still more preferably 2.0 mm or more, further preferably 2.5 mm or more
  • the laminated sheet according to any one of the above ⁇ 1> to ⁇ 6> which is preferably 30 mm or less, more preferably 10 mm or less, still more preferably 5.0 mm or less.
  • the thermoplastic polyester resin (A) is polybutylene terephthalate.
  • the plasticizer is preferably at least one member selected from the group consisting of polyester plasticizers, polyhydric alcohol ester plasticizers, polyhydric carboxylic acid ester plasticizers, and bisphenol plasticizers;
  • polystyrene-isoprene block copolymer SIS
  • polystyrene-polybutadiene copolymer SEBS
  • polystyrene-hydrogenated polybutadiene copolymer SEBS
  • polystyrene-hydrogenated polyisoprene-polystyrene block copolymer SEPS
  • polystyrene-vinyl-polyisoprene-polystyrene block copolymer SHIVS
  • polystyrene-hydrogenated polybutadiene-hydrogenated polyisoprene-polystyrene block copolymer and polystyrene-hydrogenated polybutadiene-polyiso At least one
  • the content of the thermoplastic polyester resin (A) in the ⁇ 12> polyester resin composition is preferably 50% by mass or more, more preferably 55% by mass or more, still more preferably 60% by mass or more, and preferably 90% by mass or less, more preferably 80% by mass or less, still more preferably 75% by mass or less, still more preferably 70% by mass or less; content of the plasticizer in the polyester resin composition is preferably 1% by mass or more More preferably 3% by mass or more, still more preferably 5% by mass or more, and preferably 25% by mass or less, more preferably 20% by mass or less, still more preferably 15% by mass or less; polyester resin composition
  • the content of the elastomer contained therein is preferably 5% by mass or more, more preferably 8% by mass or more, still more preferably 9.5% by mass or more.
  • the content of the inorganic filler in the polyester resin composition is preferably 5% by mass or more, more The content is preferably 10% by mass or more, more preferably 15% by mass or more, still more preferably 20% by mass or more, still more preferably 23% by mass or more, and preferably 40% by mass or less, more preferably 35% by mass or less.
  • the mass ratio of the component (B) to the inorganic filler (C) is preferably 10/90 to 60/40, more preferably 25/75 to 50.
  • ⁇ 15> The laminated sheet according to any one of the above ⁇ 1> to ⁇ 14>, wherein the flexural modulus is preferably 2.4 or more, and preferably 2.8 or less.
  • thermoplastic polyester resin and elastomer A flat test piece (40 mm ⁇ 5 mm ⁇ 0.4 mm) of a sheet-like molded product of a polyester resin composition or an elastomer, which is prepared in the same manner as described later, or a styrene isoprene block copolymer is produced.
  • a DMA device manufactured by SII, EXSTAR 6000
  • the temperature is raised from -50 ° C. to 250 ° C. at a heating rate of 2 ° C./min. Calculated as a transition point.
  • ⁇ Enthalpy of crystallization of thermoplastic polyester resin About 7 mg of a thermoplastic polyester resin sample is weighed, and the resin is heated from 25 ° C. to 300 ° C. at a temperature rising rate of 20 ° C./min according to JIS K 7122 (1999) using a DSC (Perkin Elmer Co., DSC 8500) Then, after holding for 5 minutes in that state, when cooling at ⁇ 20 ° C./min so as to be 25 ° C. or less, the enthalpy of crystallization is calculated from the exothermic peak accompanying crystallization.
  • ⁇ Styrene content of styrenic elastomer> The elastomer is dissolved in deuterated chloroform, and the H-NMR spectrum of the sample solution is measured at an observation width of 15 ppm.
  • a calibration curve is previously obtained from the peak area and concentration of styrene in the H-NMR spectrum of a polystyrene / deuterated chloroform solution of three different concentrations, and using this calibration curve, the peak area of styrene in the sample solution is used. Calculate the content.
  • Production Example 1 and Production Example 3 (Production of Sheet-Like Molding of Polyester Resin Composition)
  • the raw materials of the polyester resin composition shown in Table 1 are melt-kneaded at 240 ° C. using a co-directional meshing type twin screw extruder (TEX-28V manufactured by Japan Steel Works, Ltd.), and strand cut is performed to obtain a resin composition. Pellets were obtained. The pellets obtained were dried by dehumidification at 110 ° C. for 3 hours to make the water content 500 ppm or less.
  • TEX-28V manufactured by Japan Steel Works, Ltd.
  • the obtained pellets were fed to a 50 mm single screw extruder and melt-kneaded at 240 ° C., and then the melt-kneaded product was formed into a sheet by a roll controlled to a roll temperature of 90 ° C. and a water-cooled roll Thereafter, a sheet having a width of 450 mm and a thickness of 0.5 mm was wound up to obtain a sheet-like molded product of the polyester resin composition.
  • Production Example 2 Production of Polycarbonate Resin Composition Sheet
  • a film was formed at a barrel temperature of 260 to 300 ° C. to obtain a polycarbonate resin composition sheet having a thickness of 0.5 mm.
  • Example 1 (manufacture of laminated sheet) Two sheets of the sheet-like molded article produced in Production Example 1 and one sheet produced in Production Example 2 were prepared. One sheet was laminated on the upper surface of one sheet-like molded product, and one sheet-like molded product was laminated on the upper surface of the sheet. Next, the three laminates were integrated by heating and compressing for 1 minute under conditions of a pressure of 3 to 4 MPa using a press set to a press heating temperature of 180 ° C., and then cooled to room temperature by a cooling press . Thus, a laminated sheet having a thickness of 1.5 mm was produced.
  • the manufactured laminated sheet has a structure in which the first damping layer 2 is laminated on the upper surface of the polycarbonate layer 1 and the second damping layer 3 is laminated on the lower surface of the polycarbonate layer 1, and the cross section thereof is shown in FIG. It corresponds to the cross-sectional view of 1A.
  • Example 2 (manufacture of laminated sheet) Two sheets of the sheet-like molded article produced in Production Example 1 and two sheets produced in Production Example 2 were prepared. One sheet-like molded body was laminated on the upper surface of one sheet, one sheet was laminated on the upper surface of the sheet-like molded body, and one sheet-like molded body was laminated on the upper surface of the sheet. Next, the four laminates were integrated by heating and compressing under the same conditions as in Production Example 1 and then cooled to room temperature by a cooling press. Thus, a laminated sheet having a thickness of 2.0 mm was produced.
  • the first damping layer 2 is laminated on the upper surface of the polycarbonate layer 1
  • the second damping layer 3 is laminated on the lower surface of the polycarbonate layer 1
  • the second damping layer 3 is further formed. It is the structure where the polycarbonate layer 5 is laminated on the lower surface, and the cross section corresponds to the cross sectional view of FIG. 1C.
  • Comparative Example 1 (Production of Laminated Sheet) Three sheets produced in Production Example 2 were prepared. Two sheets were laminated on the upper surface of one sheet. Next, the three laminates were integrated by heating and compressing under the same conditions as in Production Example 1 and then cooled to room temperature by a cooling press. Thus, a laminated sheet having a thickness of 1.5 mm was produced.
  • the manufactured laminated sheet has a structure comprising the polycarbonate layer 1 in which three polycarbonate layers are laminated and integrated, and the cross section corresponds to the cross sectional view of FIG. 2A.
  • Comparative Example 2 (Production of Laminated Sheet) One sheet of the sheet-like molded product produced in Production Example 1 and two sheets produced in Production Example 2 were prepared. One sheet-like molded product was laminated on the upper surface of one sheet, and one sheet was laminated on the upper surface of the sheet-like molded product. Next, the three laminates were integrated by heating and compressing under the same conditions as in Production Example 1 and then cooled to room temperature by a cooling press. Thus, a laminated sheet having a thickness of 1.5 mm was produced.
  • the manufactured laminated sheet has a structure in which the polycarbonate layer 4 is laminated on the upper surface of the damping layer 6, and the polycarbonate layer 5 is laminated on the lower surface of the damping layer 6, and the cross section corresponds to the cross sectional view of FIG. It was
  • Comparative Example 3 (Production of Laminated Sheet) Three sheet-like molded articles produced in Production Example 1 were prepared. Two sheets of one sheet-like compact were laminated on the upper surface of one sheet-like compact. Next, the three laminates were integrated by heating and compressing under the same conditions as in Production Example 1 and then cooled to room temperature by a cooling press. Thus, a laminated sheet having a thickness of 1.5 mm was produced.
  • the manufactured laminated sheet has a structure including the vibration control layer 6 in which three vibration control layers are stacked and integrated, and the cross section corresponds to the cross sectional view of FIG. 2C.
  • Comparative Example 4 (Production of Laminated Sheet) Two sheets of the sheet-like molded article produced in Production Example 1 and two sheets produced in Production Example 2 were prepared. One sheet-like molded body was laminated on the upper surface of one sheet, one sheet-like molded body was laminated on the upper surface of the sheet-like molded body, and one sheet was laminated on the upper surface of the sheet-like molded body. Next, the four laminates were integrated by heating and compressing under the same conditions as in Production Example 1 and then cooled to room temperature by a cooling press. Thus, a laminated sheet having a thickness of 2.0 mm was produced.
  • the manufactured laminated sheet has a structure in which a damping layer 6 in which two sheet-like molded articles are integrated is laminated on the upper surface of the polycarbonate layer 5, and the polycarbonate layer 4 is laminated on the upper surface of the damping layer 6.
  • the cross section corresponds to that of FIG. 2D.
  • Example 3 (manufacture of laminated sheet) Two sheets of the sheet-like molded article produced in Production Example 1 and three sheets produced in Production Example 2 were prepared. One sheet-like molded body is laminated on the upper surface of one sheet, one sheet is laminated on the upper surface of the sheet-like molded body, one sheet-like molded body is laminated on the upper surface of the sheet, and the sheet One sheet was laminated on the upper surface of the green molded body. Next, the five laminates were integrated by heating and compressing under the same conditions as in Production Example 1, and then cooled to room temperature by a cooling press. Thus, a laminated sheet having a thickness of 2.5 mm was produced.
  • the first damping layer 2 is laminated on the upper surface of the polycarbonate layer 1, and the polycarbonate layer 4 is further laminated on the upper surface of the first damping layer 2.
  • the damping layer 3 is laminated, and the polycarbonate layer 5 is further laminated on the lower surface of the second damping layer 3, and the cross section corresponds to the cross sectional view of FIG. 1D.
  • Example 4 (manufacture of laminated sheet) Three sheets of the sheet-like molded article produced in Production Example 1 and two sheets produced in Production Example 2 were prepared. One sheet is laminated on the upper surface of one sheet-like molded product, one sheet-like molded product is laminated on the upper surface of the sheet, one sheet is laminated on the upper surface of the sheet-like molded product, and the sheet One sheet-like compact was laminated on the upper surface of the sheet. Next, the five laminates were integrated by heating and compressing under the same conditions as in Production Example 1, and then cooled to room temperature by a cooling press. Thus, a laminated sheet having a thickness of 2.5 mm was produced.
  • the first damping layer 2 is laminated on the upper surface of the polycarbonate layer 1
  • the second damping layer 3 is laminated on the lower surface of the polycarbonate layer 1
  • the first damping layer 2 is formed. It has a structure in which an additional polycarbonate layer 4 is laminated on the upper surface and an additional damping layer 6 is laminated on the upper surface of the additional polycarbonate layer 4, and the cross section corresponds to the cross sectional view of FIG. 3A. .
  • Example 5 (manufacture of laminated sheet)
  • One sheet produced in Production Example 2 and two sheet-like molded articles produced in Production Example 3 were prepared.
  • One sheet was laminated on the upper surface of one sheet-like molded product, and one sheet-like molded product was laminated on the upper surface of the sheet.
  • the three laminates were integrated by heating and compressing for 1 minute under conditions of a pressure of 3 to 4 MPa using a press set to a press heating temperature of 180 ° C., and then cooled to room temperature by a cooling press .
  • a laminated sheet having a thickness of 1.5 mm was produced.
  • the manufactured laminated sheet has a structure in which the first damping layer 2 is laminated on the upper surface of the polycarbonate layer 1 and the second damping layer 3 is laminated on the lower surface of the polycarbonate layer 1, and the cross section thereof is shown in FIG. It corresponds to the cross-sectional view of 1A.
  • Test Example 1 Each laminated sheet is cut into a size of 127 mm ⁇ 12.7 mm ⁇ thickness (1.5 to 2.0) mm (the thickness depends on the thickness of the laminated sheet obtained in each example and comparative example), and flat plate test pieces And The loss factor of the flat plate test piece was calculated by the half width method from the peak of the secondary resonance of the frequency response function measured by the central excitation method based on JIS K 7391.
  • the oscillator was Type 3160
  • the amplifier was Type 2718
  • the exciter was Type 4810
  • the acceleration sensor was Type 8001 (all manufactured by B & K)
  • MS18143 was used.
  • the measurement environment was controlled by a thermostatic bath (manufactured by ESPEC, PU-3J), and was measured at 23 ° C. As the loss factor of the laminated sheet is higher, it can be judged that the vibration damping is faster, that is, the damping effect of the laminated sheet is higher.
  • Test Example 2 (Stiffness) Each laminated sheet was cut into a size of 30 mm ⁇ 25 mm ⁇ thickness (1.5 to 2.0) mm (the thickness depends on the thickness of the laminated sheet obtained in each of the examples and comparative examples) to obtain flat test pieces. .
  • a flat plate test piece was subjected to a bending test at a distance between supporting points of 24 mm and a test speed of 1 mm / min using a TENSILON universal material tester (RTC-1250A manufactured by Orientec Co., Ltd.) based on JIS K7171.
  • the flexural modulus was determined. When the bending elastic modulus is 2.0 GPa or more, it can be judged that the bending elastic modulus is high and the rigidity is good.
  • the laminated sheet (of the example) of the present invention has a high loss coefficient and a high elastic modulus, and is excellent in both the self-supporting property and the damping effect. In addition, sufficient stiffness and impact strength are expected to be high.
  • the laminated sheet (comparative example 1) formed only from the polycarbonate layer is poor in the damping effect because the loss coefficient is low
  • the laminated sheet (comparative example 3) formed only from the damping layer is It was found that the rigidity is low because the elastic modulus is low.
  • the laminated sheet of the present invention has sufficient rigidity and impact strength to have a polycarbonate layer, and also has a high loss coefficient and is excellent in the damping effect, so for example, a speaker, a television, a radio cassette player, a headphone, an audio component Alternatively, it can be suitably used as a material for an acoustic device such as a microphone, an electric product, a product such as a vehicle, a building, an industrial device or a part thereof, or a damping material for a housing.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • General Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Physics & Mathematics (AREA)
  • Acoustics & Sound (AREA)
  • Aviation & Aerospace Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Laminated Bodies (AREA)
  • Vibration Prevention Devices (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

La présente invention concerne une feuille stratifiée, laquelle feuille comprend une structure stratifiée dans laquelle une première couche d'amortissement (2) est stratifiée sur la surface supérieure d'une couche de polycarbonate (1), tandis qu'une seconde couche d'amortissement (3) est stratifiée sur la surface inférieure de ladite couche de polycarbonate, les première et seconde couches d'amortissement étant chacune constituées par un corps formé sous la forme d'une feuille d'une composition de résine de polyester qui comprend : une résine de polyester thermoplastique (A) comprenant un composant qui comprend un composant d'acide dicarboxylique et un composant de diol ; un composant (B) qui est un plastifiant et/ou un élastomère ; et une charge minérale (C). La feuille stratifiée selon la présente invention a une rigidité et une résistance à l'impact suffisantes du fait qu'elle a la couche de polycarbonate dans celle-ci, et elle présente en outre un excellent effet d'amortissement du fait qu'elle a un coefficient de perte élevé, et, par conséquent, cette feuille stratifiée peut être utilisée de manière appropriée en tant que matériau pour un équipement audio tel que des haut-parleurs, des télévisions, des radiocassettes, des écouteurs, des composants audio et des microphones, ou en tant que matériau d'amortissement pour des produits tels que des accessoires, des véhicules, des structures architecturales et des machines industrielles, ou des composants de ceux-ci, ou des enceintes de ceux-ci.
PCT/JP2018/032430 2017-09-06 2018-08-31 Feuille stratifiée Ceased WO2019049793A1 (fr)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07196992A (ja) * 1993-12-28 1995-08-01 Nippon Autom Kk 制振シート
JP2016089148A (ja) * 2014-10-31 2016-05-23 花王株式会社 制振材料用のポリエステル樹脂組成物

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JPH05147096A (ja) * 1991-11-28 1993-06-15 Nippon Steel Chem Co Ltd 熱可塑性樹脂多層構造体
JPH08176352A (ja) * 1994-12-22 1996-07-09 Ntn Corp 制振性弾性体組成物
US6132882A (en) * 1996-12-16 2000-10-17 3M Innovative Properties Company Damped glass and plastic laminates
EP2803648B1 (fr) * 2012-01-13 2018-08-22 Sekisui Chemical Co., Ltd. Film intermédiaire pour verre feuilleté, et verre feuilleté
WO2016076337A1 (fr) * 2014-11-10 2016-05-19 株式会社クラレ Film intermédiaire pour verre feuilleté et verre feuilleté

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07196992A (ja) * 1993-12-28 1995-08-01 Nippon Autom Kk 制振シート
JP2016089148A (ja) * 2014-10-31 2016-05-23 花王株式会社 制振材料用のポリエステル樹脂組成物

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